ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
CNHFAHCC_00001 | 6e-252 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
CNHFAHCC_00002 | 6.1e-205 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
CNHFAHCC_00003 | 2.4e-33 | yaaA | S | S4 domain | ||
CNHFAHCC_00004 | 1.4e-206 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
CNHFAHCC_00005 | 1.8e-37 | yaaB | S | Domain of unknown function (DUF370) | ||
CNHFAHCC_00006 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
CNHFAHCC_00007 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
CNHFAHCC_00008 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00011 | 2.7e-182 | yaaC | S | YaaC-like Protein | ||
CNHFAHCC_00012 | 1.8e-273 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
CNHFAHCC_00013 | 5.2e-248 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
CNHFAHCC_00014 | 2.2e-157 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
CNHFAHCC_00015 | 8e-108 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
CNHFAHCC_00016 | 4.3e-207 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
CNHFAHCC_00017 | 1.3e-09 | |||||
CNHFAHCC_00018 | 2.2e-122 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
CNHFAHCC_00019 | 3.2e-115 | dgk | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxyguanosine kinase | |
CNHFAHCC_00020 | 5.6e-215 | yaaH | M | Glycoside Hydrolase Family | ||
CNHFAHCC_00021 | 2.4e-98 | yaaI | Q | COG1335 Amidases related to nicotinamidase | ||
CNHFAHCC_00022 | 1e-84 | tadA | 3.5.4.1, 3.5.4.3, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
CNHFAHCC_00023 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
CNHFAHCC_00024 | 5.3e-37 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
CNHFAHCC_00025 | 3.9e-110 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
CNHFAHCC_00026 | 7.9e-32 | yaaL | S | Protein of unknown function (DUF2508) | ||
CNHFAHCC_00027 | 3.7e-36 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
CNHFAHCC_00028 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00031 | 3.4e-31 | csfB | S | Inhibitor of sigma-G Gin | ||
CNHFAHCC_00032 | 4.7e-103 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
CNHFAHCC_00033 | 4.5e-203 | yaaN | P | Belongs to the TelA family | ||
CNHFAHCC_00034 | 1.1e-275 | adiA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | Orn Lys Arg decarboxylase | |
CNHFAHCC_00035 | 3.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
CNHFAHCC_00036 | 2.2e-54 | yaaQ | S | protein conserved in bacteria | ||
CNHFAHCC_00037 | 1.5e-71 | yaaR | S | protein conserved in bacteria | ||
CNHFAHCC_00038 | 2.2e-182 | holB | 2.7.7.7 | L | DNA polymerase III | |
CNHFAHCC_00039 | 2.1e-146 | yaaT | S | stage 0 sporulation protein | ||
CNHFAHCC_00040 | 4.8e-31 | yabA | L | Involved in initiation control of chromosome replication | ||
CNHFAHCC_00041 | 2.5e-138 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
CNHFAHCC_00042 | 1.5e-49 | yazA | L | endonuclease containing a URI domain | ||
CNHFAHCC_00043 | 4.3e-158 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
CNHFAHCC_00044 | 8.8e-44 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
CNHFAHCC_00045 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
CNHFAHCC_00046 | 1.8e-144 | tatD | L | hydrolase, TatD | ||
CNHFAHCC_00047 | 4.3e-194 | rpfB | GH23 | T | protein conserved in bacteria | |
CNHFAHCC_00048 | 8.4e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
CNHFAHCC_00049 | 2.4e-156 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
CNHFAHCC_00050 | 3.3e-137 | yabG | S | peptidase | ||
CNHFAHCC_00051 | 7.8e-39 | veg | S | protein conserved in bacteria | ||
CNHFAHCC_00052 | 2e-26 | sspF | S | DNA topological change | ||
CNHFAHCC_00053 | 4.1e-161 | ispE | 2.1.1.182, 2.7.1.148 | I | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
CNHFAHCC_00054 | 2.6e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
CNHFAHCC_00055 | 3.8e-63 | yabJ | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | |
CNHFAHCC_00056 | 1e-47 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
CNHFAHCC_00058 | 6.6e-230 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
CNHFAHCC_00059 | 9.4e-175 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
CNHFAHCC_00060 | 3.9e-97 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
CNHFAHCC_00061 | 8e-105 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
CNHFAHCC_00062 | 2.4e-39 | yabK | S | Peptide ABC transporter permease | ||
CNHFAHCC_00063 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
CNHFAHCC_00064 | 1.5e-92 | spoVT | K | stage V sporulation protein | ||
CNHFAHCC_00065 | 2.4e-287 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
CNHFAHCC_00066 | 2.7e-245 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
CNHFAHCC_00067 | 1.1e-37 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
CNHFAHCC_00068 | 1.5e-49 | yabP | S | Sporulation protein YabP | ||
CNHFAHCC_00069 | 3.9e-108 | yabQ | S | spore cortex biosynthesis protein | ||
CNHFAHCC_00070 | 3.7e-48 | divIC | D | Septum formation initiator | ||
CNHFAHCC_00071 | 8.5e-58 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
CNHFAHCC_00074 | 0.0 | spoIIE | 3.1.3.16, 3.1.3.3 | KT | stage II sporulation protein E | |
CNHFAHCC_00075 | 1.5e-124 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
CNHFAHCC_00076 | 6.7e-187 | KLT | serine threonine protein kinase | |||
CNHFAHCC_00077 | 3.5e-274 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
CNHFAHCC_00078 | 7.9e-94 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
CNHFAHCC_00079 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
CNHFAHCC_00080 | 1.5e-146 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
CNHFAHCC_00081 | 2.9e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
CNHFAHCC_00082 | 1.6e-160 | yacD | 5.2.1.8 | O | peptidyl-prolyl isomerase | |
CNHFAHCC_00083 | 8.9e-170 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
CNHFAHCC_00084 | 4.7e-271 | pabB | 2.6.1.85 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
CNHFAHCC_00085 | 1.5e-106 | pabA | 2.6.1.85, 4.1.3.27 | EH | Anthranilate synthase | |
CNHFAHCC_00086 | 1.6e-168 | pabC | 2.6.1.42, 4.1.3.38 | EH | 4-amino-4-deoxychorismate lyase | |
CNHFAHCC_00087 | 2.6e-160 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
CNHFAHCC_00088 | 8.2e-63 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
CNHFAHCC_00089 | 2.7e-88 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
CNHFAHCC_00090 | 4.1e-30 | yazB | K | transcriptional | ||
CNHFAHCC_00091 | 3.7e-190 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
CNHFAHCC_00092 | 1.3e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
CNHFAHCC_00093 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00098 | 2e-08 | |||||
CNHFAHCC_00103 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00104 | 2.9e-76 | ctsR | K | Belongs to the CtsR family | ||
CNHFAHCC_00105 | 4.7e-47 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
CNHFAHCC_00106 | 6.1e-202 | mcsB | 2.7.14.1, 2.7.3.2, 2.7.3.3 | E | Catalyzes the specific phosphorylation of arginine residues in a large number of proteins. Is part of the bacterial stress response system. Protein arginine phosphorylation has a physiologically important role and is involved in the regulation of many critical cellular processes, such as protein homeostasis, motility, competence, and stringent and stress responses, by regulating gene expression and protein activity | |
CNHFAHCC_00107 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
CNHFAHCC_00108 | 4.6e-233 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
CNHFAHCC_00109 | 1.3e-196 | disA | 2.7.7.85 | L | Has also diadenylate cyclase activity, catalyzing the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP). c- di-AMP acts as a signaling molecule that couples DNA integrity with progression of sporulation. The rise in c-di-AMP level generated by DisA while scanning the chromosome, operates as a positive signal that advances sporulation | |
CNHFAHCC_00110 | 2.7e-197 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
CNHFAHCC_00111 | 3.8e-125 | ispD | 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
CNHFAHCC_00112 | 3.1e-86 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
CNHFAHCC_00113 | 1.9e-280 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
CNHFAHCC_00114 | 1.1e-115 | cysE | 2.3.1.30 | E | Serine acetyltransferase | |
CNHFAHCC_00115 | 4.9e-273 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
CNHFAHCC_00116 | 1e-72 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
CNHFAHCC_00117 | 1.2e-135 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
CNHFAHCC_00118 | 1.2e-88 | yacP | S | RNA-binding protein containing a PIN domain | ||
CNHFAHCC_00119 | 1.5e-115 | sigH | K | Belongs to the sigma-70 factor family | ||
CNHFAHCC_00120 | 1e-21 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
CNHFAHCC_00121 | 5.2e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
CNHFAHCC_00122 | 2.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
CNHFAHCC_00123 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
CNHFAHCC_00124 | 5.1e-79 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
CNHFAHCC_00125 | 1.3e-42 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
CNHFAHCC_00126 | 8.2e-108 | rsmC | 2.1.1.172 | J | Methyltransferase | |
CNHFAHCC_00127 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_00128 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_00129 | 8e-33 | ybxF | J | Belongs to the eukaryotic ribosomal protein eL8 family | ||
CNHFAHCC_00130 | 8.5e-72 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
CNHFAHCC_00131 | 6e-82 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
CNHFAHCC_00132 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
CNHFAHCC_00133 | 2.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
CNHFAHCC_00134 | 9.1e-186 | ybaC | 3.4.11.5 | S | Alpha/beta hydrolase family | |
CNHFAHCC_00135 | 7.5e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
CNHFAHCC_00136 | 6.3e-111 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
CNHFAHCC_00137 | 3e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
CNHFAHCC_00138 | 1.2e-43 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
CNHFAHCC_00139 | 1.5e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
CNHFAHCC_00140 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
CNHFAHCC_00141 | 4.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
CNHFAHCC_00142 | 6.2e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
CNHFAHCC_00143 | 1.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
CNHFAHCC_00144 | 1.7e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
CNHFAHCC_00145 | 3.5e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
CNHFAHCC_00146 | 3.9e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
CNHFAHCC_00147 | 6.2e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
CNHFAHCC_00148 | 4.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
CNHFAHCC_00149 | 3.4e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
CNHFAHCC_00150 | 3.9e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
CNHFAHCC_00151 | 1.3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
CNHFAHCC_00152 | 4e-57 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
CNHFAHCC_00153 | 3.1e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
CNHFAHCC_00154 | 1.9e-23 | rpmD | J | Ribosomal protein L30 | ||
CNHFAHCC_00155 | 1.8e-72 | rplO | J | binds to the 23S rRNA | ||
CNHFAHCC_00156 | 8e-230 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
CNHFAHCC_00157 | 5.7e-123 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
CNHFAHCC_00158 | 3.7e-142 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
CNHFAHCC_00159 | 1.1e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
CNHFAHCC_00160 | 4.2e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
CNHFAHCC_00161 | 3.1e-57 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
CNHFAHCC_00162 | 2.1e-64 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
CNHFAHCC_00163 | 3.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_00164 | 3.6e-58 | rplQ | J | Ribosomal protein L17 | ||
CNHFAHCC_00165 | 5.1e-156 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
CNHFAHCC_00166 | 1.7e-154 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
CNHFAHCC_00167 | 4.7e-119 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
CNHFAHCC_00168 | 2.8e-142 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
CNHFAHCC_00169 | 6.4e-78 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
CNHFAHCC_00170 | 4.7e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
CNHFAHCC_00171 | 8.2e-145 | ybaJ | Q | Methyltransferase domain | ||
CNHFAHCC_00172 | 9.7e-66 | ybaK | S | Protein of unknown function (DUF2521) | ||
CNHFAHCC_00173 | 1.1e-132 | cwlD | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
CNHFAHCC_00174 | 1.4e-198 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
CNHFAHCC_00175 | 1.2e-84 | gerD | ||||
CNHFAHCC_00176 | 1.5e-102 | kbaA | 2.7.8.43 | S | Involved in the activation of the KinB signaling pathway of sporulation | |
CNHFAHCC_00177 | 1.2e-140 | pdaB | 3.5.1.104 | G | Polysaccharide deacetylase | |
CNHFAHCC_00178 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00179 | 3.3e-39 | S | COG NOG15344 non supervised orthologous group | |||
CNHFAHCC_00182 | 2e-08 | |||||
CNHFAHCC_00186 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00187 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00188 | 3.9e-249 | ybaR | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | ||
CNHFAHCC_00190 | 1.2e-161 | ybaS | 1.1.1.58 | S | Na -dependent transporter | |
CNHFAHCC_00191 | 2.2e-142 | ybbA | S | Putative esterase | ||
CNHFAHCC_00192 | 3e-179 | feuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00193 | 1.1e-176 | feuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00194 | 7.2e-167 | feuA | P | Iron-uptake system-binding protein | ||
CNHFAHCC_00195 | 5.4e-308 | ybbB | K | COG2207 AraC-type DNA-binding domain-containing proteins | ||
CNHFAHCC_00196 | 4.4e-241 | ybbC | 3.2.1.52 | S | protein conserved in bacteria | |
CNHFAHCC_00197 | 0.0 | ybbD | 3.2.1.52 | G | Belongs to the glycosyl hydrolase 3 family | |
CNHFAHCC_00198 | 4e-256 | yfeW | 3.4.16.4 | V | Belongs to the UPF0214 family | |
CNHFAHCC_00199 | 9.8e-234 | ybbF | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_00200 | 1.1e-150 | ybbH | K | transcriptional | ||
CNHFAHCC_00201 | 2.1e-163 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
CNHFAHCC_00202 | 6.4e-87 | ybbJ | J | acetyltransferase | ||
CNHFAHCC_00203 | 3.9e-78 | ybbK | 2.4.2.1, 6.3.2.4 | S | Protein of unknown function (DUF523) | |
CNHFAHCC_00209 | 8.5e-99 | sigW | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_00210 | 1.7e-103 | rsiW | K | Is the anti-sigma factor for SigW. The presence of RsiW leads to the inactivation of SigW, and its proteolytic destruction to sigma-W activation | ||
CNHFAHCC_00211 | 2.7e-146 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
CNHFAHCC_00212 | 3e-225 | ybbR | S | protein conserved in bacteria | ||
CNHFAHCC_00213 | 9.3e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
CNHFAHCC_00214 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
CNHFAHCC_00215 | 2.1e-176 | alkA | 3.2.2.21 | L | COG0122 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
CNHFAHCC_00216 | 1.4e-121 | adaA | 3.2.2.21 | K | Transcriptional regulator | |
CNHFAHCC_00217 | 5.1e-101 | ogt | 2.1.1.63, 3.2.2.21 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
CNHFAHCC_00218 | 1.5e-278 | ndhF | 1.6.5.3 | CP | COG1009 NADH ubiquinone oxidoreductase subunit 5 (chain L) Multisubunit Na H antiporter, MnhA subunit | |
CNHFAHCC_00219 | 0.0 | ybcC | S | Belongs to the UPF0753 family | ||
CNHFAHCC_00220 | 4.6e-96 | can | 4.2.1.1 | P | carbonic anhydrase | |
CNHFAHCC_00221 | 3.9e-47 | |||||
CNHFAHCC_00222 | 4.7e-61 | ybcI | S | Uncharacterized conserved protein (DUF2294) | ||
CNHFAHCC_00224 | 5.1e-50 | ybzH | K | Helix-turn-helix domain | ||
CNHFAHCC_00225 | 2e-203 | ybcL | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00226 | 1.5e-49 | glmD | 2.6.1.16 | M | glutamine-fructose-6-phosphate transaminase (isomerizing) activity | |
CNHFAHCC_00228 | 9.1e-239 | J | 4Fe-4S single cluster domain | |||
CNHFAHCC_00229 | 1.6e-277 | V | CAAX protease self-immunity | |||
CNHFAHCC_00230 | 1.9e-135 | skfE | V | ABC transporter | ||
CNHFAHCC_00231 | 4e-248 | skfF | S | ABC transporter | ||
CNHFAHCC_00232 | 7.8e-91 | C | HEAT repeats | |||
CNHFAHCC_00233 | 9.6e-79 | txn | CO | Thioredoxin-like | ||
CNHFAHCC_00234 | 6.2e-182 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
CNHFAHCC_00235 | 1.5e-123 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_00236 | 1.8e-173 | T | His Kinase A (phospho-acceptor) domain | |||
CNHFAHCC_00238 | 1.6e-140 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_00239 | 4.8e-154 | ybdN | ||||
CNHFAHCC_00240 | 1.5e-217 | ybdO | S | Domain of unknown function (DUF4885) | ||
CNHFAHCC_00241 | 2.4e-259 | yifK | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_00242 | 3.7e-38 | csgA | S | Sigma-G-dependent sporulation-specific SASP protein | ||
CNHFAHCC_00243 | 4.9e-30 | ybxH | S | Family of unknown function (DUF5370) | ||
CNHFAHCC_00244 | 7.2e-152 | ybxI | 3.5.2.6 | V | beta-lactamase | |
CNHFAHCC_00245 | 1.4e-247 | cypC | 1.11.2.4, 1.14.14.1 | Q | Cytochrome P450 | |
CNHFAHCC_00246 | 4.9e-41 | ybyB | ||||
CNHFAHCC_00247 | 1.8e-290 | ybeC | E | amino acid | ||
CNHFAHCC_00248 | 5.6e-166 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
CNHFAHCC_00249 | 7.3e-258 | glpT | G | -transporter | ||
CNHFAHCC_00250 | 2.9e-35 | S | Protein of unknown function (DUF2651) | |||
CNHFAHCC_00251 | 1.6e-171 | ybfA | 3.4.15.5 | K | FR47-like protein | |
CNHFAHCC_00252 | 2.2e-224 | ybfB | G | COG0477 Permeases of the major facilitator superfamily | ||
CNHFAHCC_00254 | 0.0 | ybfG | 3.2.1.132 | M | Domain of unknown function (DUF1906) | |
CNHFAHCC_00255 | 8.8e-162 | ybfH | EG | EamA-like transporter family | ||
CNHFAHCC_00256 | 2.3e-145 | msmR | K | AraC-like ligand binding domain | ||
CNHFAHCC_00257 | 1.9e-214 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
CNHFAHCC_00258 | 6.9e-178 | mpr | 3.4.21.19 | M | Belongs to the peptidase S1B family | |
CNHFAHCC_00260 | 2.5e-169 | S | Alpha/beta hydrolase family | |||
CNHFAHCC_00261 | 3.2e-95 | pssA | 2.7.8.8 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
CNHFAHCC_00262 | 2.7e-85 | ybfM | S | SNARE associated Golgi protein | ||
CNHFAHCC_00263 | 5.6e-149 | psd | 4.1.1.65 | I | Catalyzes the formation of phosphatidylethanolamine (PtdEtn) from phosphatidylserine (PtdSer) | |
CNHFAHCC_00264 | 3.2e-46 | ybfN | ||||
CNHFAHCC_00265 | 4.3e-258 | S | Erythromycin esterase | |||
CNHFAHCC_00266 | 6.7e-167 | ybfP | K | Transcriptional regulator | ||
CNHFAHCC_00267 | 3.9e-192 | yceA | S | Belongs to the UPF0176 family | ||
CNHFAHCC_00268 | 4.9e-216 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
CNHFAHCC_00269 | 0.0 | ptsG | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_00270 | 2.1e-137 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
CNHFAHCC_00271 | 4.9e-128 | K | UTRA | |||
CNHFAHCC_00273 | 5.5e-203 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
CNHFAHCC_00274 | 6.7e-262 | mmuP | E | amino acid | ||
CNHFAHCC_00275 | 9.3e-183 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine | |
CNHFAHCC_00276 | 2.3e-257 | agcS | E | Sodium alanine symporter | ||
CNHFAHCC_00277 | 1.5e-188 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
CNHFAHCC_00278 | 1.5e-229 | phoQ | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_00279 | 9e-170 | glnL | T | Regulator | ||
CNHFAHCC_00280 | 2.7e-174 | kdgD | 4.2.1.41 | EM | 5-dehydro-4-deoxyglucarate dehydratase activity | |
CNHFAHCC_00281 | 3.6e-274 | ycbD | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | ||
CNHFAHCC_00282 | 1.2e-255 | gudP | G | COG0477 Permeases of the major facilitator superfamily | ||
CNHFAHCC_00283 | 2.2e-270 | gudD | 4.2.1.40 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
CNHFAHCC_00284 | 1.5e-124 | ycbG | K | FCD | ||
CNHFAHCC_00285 | 3.7e-298 | garD | 4.2.1.42, 4.2.1.7 | G | Altronate | |
CNHFAHCC_00286 | 1.8e-178 | ycbJ | S | Macrolide 2'-phosphotransferase | ||
CNHFAHCC_00287 | 4.4e-24 | rtpA | K | Tryptophan RNA-binding attenuator protein inhibitory protein | ||
CNHFAHCC_00288 | 7.3e-172 | eamA1 | EG | spore germination | ||
CNHFAHCC_00289 | 2.2e-125 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_00290 | 2.4e-170 | T | PhoQ Sensor | |||
CNHFAHCC_00291 | 4.8e-168 | ycbN | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_00292 | 2.1e-115 | S | ABC-2 family transporter protein | |||
CNHFAHCC_00293 | 8.2e-53 | ycbP | S | Protein of unknown function (DUF2512) | ||
CNHFAHCC_00294 | 1.3e-78 | sleB | 3.5.1.28 | M | Cell wall | |
CNHFAHCC_00295 | 6.6e-136 | ycbR | T | vWA found in TerF C terminus | ||
CNHFAHCC_00296 | 0.0 | phoD | 3.1.3.1 | P | COG3540 Phosphodiesterase alkaline phosphatase D | |
CNHFAHCC_00297 | 5e-28 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
CNHFAHCC_00298 | 1.2e-124 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
CNHFAHCC_00299 | 1.4e-121 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
CNHFAHCC_00300 | 6.2e-210 | ycbU | E | Selenocysteine lyase | ||
CNHFAHCC_00301 | 9.1e-230 | lmrB | EGP | the major facilitator superfamily | ||
CNHFAHCC_00302 | 4.8e-102 | yxaF | K | Transcriptional regulator | ||
CNHFAHCC_00303 | 2.2e-202 | ansB | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
CNHFAHCC_00304 | 5.6e-115 | lip | 3.1.1.3 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |
CNHFAHCC_00305 | 2e-59 | S | RDD family | |||
CNHFAHCC_00306 | 9.5e-200 | yccF | K | DNA-templated transcriptional preinitiation complex assembly | ||
CNHFAHCC_00307 | 2e-161 | 2.7.13.3 | T | GHKL domain | ||
CNHFAHCC_00308 | 1.2e-126 | lytR_2 | T | LytTr DNA-binding domain | ||
CNHFAHCC_00309 | 4.1e-133 | natA | 3.6.3.7 | CP | ATPases associated with a variety of cellular activities | |
CNHFAHCC_00310 | 4.5e-203 | natB | CP | ABC-2 family transporter protein | ||
CNHFAHCC_00311 | 1.6e-174 | yccK | C | Aldo keto reductase | ||
CNHFAHCC_00312 | 6.6e-177 | ycdA | S | Domain of unknown function (DUF5105) | ||
CNHFAHCC_00313 | 5.9e-282 | ycdB | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_00314 | 7.4e-267 | ycdC | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_00315 | 1.7e-95 | cwlK | M | D-alanyl-D-alanine carboxypeptidase | ||
CNHFAHCC_00316 | 5.5e-174 | S | response regulator aspartate phosphatase | |||
CNHFAHCC_00317 | 1.6e-140 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_00318 | 0.0 | ycdG | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
CNHFAHCC_00319 | 6.6e-168 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
CNHFAHCC_00320 | 2.5e-132 | adcC | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
CNHFAHCC_00321 | 1.7e-135 | adcB | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
CNHFAHCC_00322 | 6.2e-179 | yceB | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_00323 | 3.9e-110 | yceC | 3.5.4.33 | T | proteins involved in stress response, homologs of TerZ and | |
CNHFAHCC_00324 | 2.8e-105 | yceD | T | proteins involved in stress response, homologs of TerZ and | ||
CNHFAHCC_00325 | 4.6e-108 | yceE | T | proteins involved in stress response, homologs of TerZ and | ||
CNHFAHCC_00326 | 6.3e-137 | terC | P | Protein of unknown function (DUF475) | ||
CNHFAHCC_00327 | 0.0 | yceG | S | Putative component of 'biosynthetic module' | ||
CNHFAHCC_00328 | 2e-192 | yceH | P | Belongs to the TelA family | ||
CNHFAHCC_00329 | 1e-218 | naiP | P | Uncharacterised MFS-type transporter YbfB | ||
CNHFAHCC_00330 | 1.9e-209 | yceJ | EGP | Uncharacterised MFS-type transporter YbfB | ||
CNHFAHCC_00331 | 1.6e-45 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
CNHFAHCC_00332 | 5.1e-229 | proV | 3.6.3.32 | E | glycine betaine | |
CNHFAHCC_00333 | 1.3e-127 | opuAB | P | glycine betaine | ||
CNHFAHCC_00334 | 5.3e-164 | opuAC | E | glycine betaine | ||
CNHFAHCC_00335 | 1.2e-219 | amhX | S | amidohydrolase | ||
CNHFAHCC_00336 | 1e-257 | ycgA | S | Membrane | ||
CNHFAHCC_00337 | 1.1e-98 | ycgB | ||||
CNHFAHCC_00338 | 0.0 | amyE | 3.2.1.1 | GH13 | G | alpha-amylase |
CNHFAHCC_00339 | 3.3e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
CNHFAHCC_00340 | 6.5e-293 | lctP | C | L-lactate permease | ||
CNHFAHCC_00341 | 6.2e-269 | mdr | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00342 | 3.4e-77 | emrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_00343 | 6.8e-113 | ycgF | E | Lysine exporter protein LysE YggA | ||
CNHFAHCC_00344 | 1.2e-151 | yqcI | S | YqcI/YcgG family | ||
CNHFAHCC_00345 | 5.6e-250 | ycgH | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_00346 | 2.4e-112 | ycgI | S | Domain of unknown function (DUF1989) | ||
CNHFAHCC_00347 | 1.5e-149 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
CNHFAHCC_00348 | 2.5e-109 | tmrB | S | AAA domain | ||
CNHFAHCC_00349 | 3e-104 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
CNHFAHCC_00350 | 3.6e-145 | yafE | Q | ubiE/COQ5 methyltransferase family | ||
CNHFAHCC_00351 | 2.2e-179 | oxyR3 | K | LysR substrate binding domain | ||
CNHFAHCC_00352 | 2.9e-184 | cah | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
CNHFAHCC_00353 | 2.9e-145 | ycgL | S | Predicted nucleotidyltransferase | ||
CNHFAHCC_00354 | 5.1e-170 | ycgM | E | Proline dehydrogenase | ||
CNHFAHCC_00355 | 7.3e-294 | rocA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
CNHFAHCC_00356 | 3.1e-262 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
CNHFAHCC_00357 | 1.6e-227 | ycgP | QT | COG2508 Regulator of polyketide synthase expression | ||
CNHFAHCC_00358 | 2.6e-147 | ycgQ | S | membrane | ||
CNHFAHCC_00359 | 1.7e-141 | ycgR | S | permeases | ||
CNHFAHCC_00360 | 5.7e-163 | I | alpha/beta hydrolase fold | |||
CNHFAHCC_00361 | 1.3e-193 | ycgT | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
CNHFAHCC_00362 | 9.3e-283 | cobA | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
CNHFAHCC_00363 | 3.9e-56 | nirD | 1.7.1.15 | P | Nitrite reductase | |
CNHFAHCC_00364 | 0.0 | nirB | 1.7.1.15 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
CNHFAHCC_00365 | 0.0 | nasC | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
CNHFAHCC_00366 | 0.0 | nirB | 1.7.1.15 | C | Assimilatory nitrate reductase (electron transfer subunit) | |
CNHFAHCC_00367 | 7.6e-222 | nasA | P | COG2223 Nitrate nitrite transporter | ||
CNHFAHCC_00368 | 1.4e-172 | folE2 | 3.5.4.16 | S | Converts GTP to 7,8-dihydroneopterin triphosphate | |
CNHFAHCC_00369 | 5.5e-109 | yciB | M | ErfK YbiS YcfS YnhG | ||
CNHFAHCC_00370 | 1.4e-228 | yciC | S | GTPases (G3E family) | ||
CNHFAHCC_00371 | 2.4e-116 | yecS | P | COG0765 ABC-type amino acid transport system, permease component | ||
CNHFAHCC_00372 | 4.4e-131 | yckB | ET | COG0834 ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
CNHFAHCC_00374 | 3.3e-77 | yckC | S | membrane | ||
CNHFAHCC_00375 | 3.5e-52 | yckD | S | Protein of unknown function (DUF2680) | ||
CNHFAHCC_00376 | 1.2e-298 | yckE | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CNHFAHCC_00377 | 3.4e-70 | nin | S | Competence protein J (ComJ) | ||
CNHFAHCC_00378 | 3.2e-72 | nucA | M | Deoxyribonuclease NucA/NucB | ||
CNHFAHCC_00379 | 3e-187 | tlpC | 2.7.13.3 | NT | chemotaxis protein | |
CNHFAHCC_00380 | 4.6e-97 | hxlB | 4.1.2.43, 5.3.1.27 | G | SIS domain | |
CNHFAHCC_00381 | 3.3e-107 | hxlA | 4.1.2.43 | G | 3-hexulose-6-phosphate synthase | |
CNHFAHCC_00382 | 1.3e-63 | hxlR | K | transcriptional | ||
CNHFAHCC_00383 | 0.0 | srfAA | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
CNHFAHCC_00384 | 0.0 | srfAB | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
CNHFAHCC_00385 | 0.0 | srfAC | Q | COG1020 Non-ribosomal peptide synthetase modules and related proteins | ||
CNHFAHCC_00386 | 5.7e-140 | srfAD | Q | thioesterase | ||
CNHFAHCC_00387 | 4.2e-228 | EGP | Major Facilitator Superfamily | |||
CNHFAHCC_00388 | 4.9e-91 | S | YcxB-like protein | |||
CNHFAHCC_00389 | 7.4e-164 | ycxC | EG | EamA-like transporter family | ||
CNHFAHCC_00390 | 4.4e-255 | ycxD | K | GntR family transcriptional regulator | ||
CNHFAHCC_00391 | 4.4e-75 | acpT | 2.7.8.7 | H | Belongs to the P-Pant transferase superfamily | |
CNHFAHCC_00392 | 4.4e-115 | yczE | S | membrane | ||
CNHFAHCC_00393 | 2.8e-134 | tcyC | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
CNHFAHCC_00394 | 6.2e-123 | tcyB | P | COG0765 ABC-type amino acid transport system, permease component | ||
CNHFAHCC_00395 | 1.5e-141 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
CNHFAHCC_00396 | 4.9e-162 | bsdA | K | LysR substrate binding domain | ||
CNHFAHCC_00397 | 2e-109 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
CNHFAHCC_00398 | 1.8e-283 | yclC | 4.1.1.61 | H | Decarboxylase involved in the decarboxylation and detoxification of phenolic derivatives under both aerobic and anaerobic conditions. It is able to catalyze the reversible decarboxylation of 4-hydroxybenzoate | |
CNHFAHCC_00399 | 4e-39 | bsdD | 4.1.1.61 | S | response to toxic substance | |
CNHFAHCC_00400 | 2.4e-80 | yclD | ||||
CNHFAHCC_00401 | 6.2e-162 | yclE | 3.4.11.5 | S | Alpha beta hydrolase | |
CNHFAHCC_00402 | 1.5e-267 | dtpT | E | amino acid peptide transporter | ||
CNHFAHCC_00403 | 2.9e-310 | yclG | M | Pectate lyase superfamily protein | ||
CNHFAHCC_00405 | 6.8e-282 | gerKA | EG | Spore germination protein | ||
CNHFAHCC_00406 | 1.3e-232 | gerKC | S | spore germination | ||
CNHFAHCC_00407 | 9.9e-200 | gerKB | F | Spore germination protein | ||
CNHFAHCC_00408 | 3.9e-122 | yclH | P | ABC transporter | ||
CNHFAHCC_00409 | 1.7e-204 | yclI | V | ABC transporter (permease) YclI | ||
CNHFAHCC_00410 | 2.4e-127 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_00411 | 1.8e-262 | yclK | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |
CNHFAHCC_00412 | 5.2e-71 | S | aspartate phosphatase | |||
CNHFAHCC_00416 | 1.5e-253 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
CNHFAHCC_00418 | 1.6e-161 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00419 | 2.6e-164 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00420 | 4.7e-137 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
CNHFAHCC_00421 | 5.5e-175 | yclQ | P | COG4607 ABC-type enterochelin transport system, periplasmic component | ||
CNHFAHCC_00422 | 1.4e-251 | ycnB | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00423 | 6.5e-154 | ycnC | K | Transcriptional regulator | ||
CNHFAHCC_00424 | 4.4e-135 | nfrA2 | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
CNHFAHCC_00425 | 1.6e-45 | ycnE | S | Monooxygenase | ||
CNHFAHCC_00426 | 2.2e-51 | yczG | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
CNHFAHCC_00427 | 1.3e-273 | gabR | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
CNHFAHCC_00428 | 4.4e-247 | gabT | 2.6.1.19, 2.6.1.22 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
CNHFAHCC_00429 | 3.4e-266 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
CNHFAHCC_00430 | 6.1e-149 | glcU | U | Glucose uptake | ||
CNHFAHCC_00431 | 9.9e-146 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_00432 | 1.3e-100 | ycnI | S | protein conserved in bacteria | ||
CNHFAHCC_00433 | 1.4e-308 | ycnJ | P | protein, homolog of Cu resistance protein CopC | ||
CNHFAHCC_00434 | 1.7e-107 | ycnK | K | COG1349 Transcriptional regulators of sugar metabolism | ||
CNHFAHCC_00435 | 7.3e-56 | |||||
CNHFAHCC_00436 | 5.6e-240 | mtlA | 2.7.1.197 | G | COG2213 Phosphotransferase system, mannitol-specific IIBC component | |
CNHFAHCC_00437 | 2e-71 | mtlF | 2.7.1.197 | G | COG4668 Mannitol fructose-specific phosphotransferase system, IIA domain | |
CNHFAHCC_00438 | 7.3e-211 | mtlD | 1.1.1.17 | G | COG0246 Mannitol-1-phosphate altronate dehydrogenases | |
CNHFAHCC_00439 | 3.8e-201 | ycsA | 1.1.1.83, 1.1.1.93, 4.1.1.73 | CE | Tartrate dehydrogenase | |
CNHFAHCC_00440 | 3.2e-10 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CNHFAHCC_00441 | 7.6e-76 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CNHFAHCC_00442 | 5e-113 | M1-673 | 3.1.1.45 | Q | COG0412 Dienelactone hydrolase and related enzymes | |
CNHFAHCC_00443 | 5.4e-68 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
CNHFAHCC_00445 | 8e-137 | ycsE | 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
CNHFAHCC_00446 | 1.2e-140 | ycsF | S | Belongs to the UPF0271 (lamB) family | ||
CNHFAHCC_00447 | 6.5e-213 | ycsG | P | COG1914 Mn2 and Fe2 transporters of the NRAMP family | ||
CNHFAHCC_00448 | 9.6e-149 | ycsI | S | Belongs to the D-glutamate cyclase family | ||
CNHFAHCC_00449 | 1.9e-135 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
CNHFAHCC_00450 | 5.1e-187 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
CNHFAHCC_00451 | 1.2e-132 | kipR | K | Transcriptional regulator | ||
CNHFAHCC_00452 | 9.9e-120 | ycsK | E | anatomical structure formation involved in morphogenesis | ||
CNHFAHCC_00454 | 1.4e-49 | yczJ | S | biosynthesis | ||
CNHFAHCC_00455 | 0.0 | pbpC | 3.4.16.4 | M | Penicillin-binding Protein | |
CNHFAHCC_00456 | 2.8e-176 | ydhF | S | Oxidoreductase | ||
CNHFAHCC_00457 | 0.0 | mtlR | K | transcriptional regulator, MtlR | ||
CNHFAHCC_00458 | 1.4e-294 | ydaB | IQ | acyl-CoA ligase | ||
CNHFAHCC_00459 | 1.1e-99 | ydaC | Q | Methyltransferase domain | ||
CNHFAHCC_00460 | 1.4e-161 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_00461 | 1.2e-96 | MA20_27600 | 5.3.1.15 | S | Cupin 2, conserved barrel domain protein | |
CNHFAHCC_00462 | 5e-104 | rimL | 1.1.1.25 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
CNHFAHCC_00463 | 6.8e-77 | ydaG | 1.4.3.5 | S | general stress protein | |
CNHFAHCC_00464 | 4.1e-139 | amj | U | Involved in peptidoglycan biosynthesis. Transports lipid-linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane | ||
CNHFAHCC_00465 | 5.1e-47 | ydzA | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00466 | 2.5e-74 | lrpC | K | Transcriptional regulator | ||
CNHFAHCC_00467 | 0.0 | topB | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
CNHFAHCC_00468 | 1.9e-208 | ydaJ | M | Belongs to the glycosyl hydrolase 8 (cellulase D) family | ||
CNHFAHCC_00469 | 2e-152 | ydaK | T | Diguanylate cyclase, GGDEF domain | ||
CNHFAHCC_00470 | 0.0 | ydaL | S | Uncharacterized protein conserved in bacteria (DUF2334) | ||
CNHFAHCC_00471 | 4.5e-233 | ydaM | M | Glycosyl transferase family group 2 | ||
CNHFAHCC_00472 | 0.0 | ydaN | S | Bacterial cellulose synthase subunit | ||
CNHFAHCC_00473 | 0.0 | ydaO | E | amino acid | ||
CNHFAHCC_00474 | 4.6e-79 | mutT | 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
CNHFAHCC_00475 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
CNHFAHCC_00477 | 9.4e-40 | |||||
CNHFAHCC_00478 | 1e-224 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
CNHFAHCC_00480 | 3.3e-77 | ydaT | S | Uncharacterized protein conserved in bacteria (DUF2188) | ||
CNHFAHCC_00481 | 3.8e-148 | ydbA | 3.6.3.4, 3.6.3.54 | P | EcsC protein family | |
CNHFAHCC_00483 | 8.9e-59 | ydbB | G | Cupin domain | ||
CNHFAHCC_00484 | 2.8e-63 | ydbC | S | Domain of unknown function (DUF4937 | ||
CNHFAHCC_00485 | 3.2e-155 | ydbD | P | Catalase | ||
CNHFAHCC_00486 | 2.7e-199 | dctB | G | COG1638 TRAP-type C4-dicarboxylate transport system, periplasmic component | ||
CNHFAHCC_00487 | 2.5e-297 | dctS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
CNHFAHCC_00488 | 8.1e-120 | dctR | T | COG4565 Response regulator of citrate malate metabolism | ||
CNHFAHCC_00489 | 6.3e-227 | dctA | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
CNHFAHCC_00490 | 4.4e-181 | ydbI | S | AI-2E family transporter | ||
CNHFAHCC_00492 | 3.6e-171 | ydbJ | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_00493 | 5.5e-125 | ydbK | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | ||
CNHFAHCC_00494 | 2.7e-52 | ydbL | ||||
CNHFAHCC_00495 | 1.6e-213 | ydbM | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
CNHFAHCC_00496 | 2.5e-18 | S | Fur-regulated basic protein B | |||
CNHFAHCC_00497 | 2.2e-07 | S | Fur-regulated basic protein A | |||
CNHFAHCC_00498 | 6.4e-146 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
CNHFAHCC_00499 | 8.6e-56 | ydbP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
CNHFAHCC_00500 | 1.8e-198 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
CNHFAHCC_00501 | 3.7e-247 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
CNHFAHCC_00502 | 1e-244 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
CNHFAHCC_00503 | 3e-81 | ydbS | S | Bacterial PH domain | ||
CNHFAHCC_00504 | 3.3e-243 | ydbT | S | Membrane | ||
CNHFAHCC_00505 | 4.9e-105 | ydcA | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
CNHFAHCC_00506 | 1.1e-54 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
CNHFAHCC_00507 | 1.1e-181 | ydcC | M | COG2834 Outer membrane lipoprotein-sorting protein | ||
CNHFAHCC_00508 | 2.3e-223 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
CNHFAHCC_00509 | 4.8e-42 | ndoAI | K | transcriptional regulators containing the CopG Arc MetJ DNA-binding domain and a metal-binding domain | ||
CNHFAHCC_00510 | 2.5e-56 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
CNHFAHCC_00511 | 1.3e-143 | rsbR | T | Positive regulator of sigma-B | ||
CNHFAHCC_00512 | 5.2e-57 | rsbS | T | antagonist | ||
CNHFAHCC_00513 | 1.3e-69 | rsbT | 2.7.11.1 | T | COG2172 Anti-sigma regulatory factor (Ser Thr protein kinase) | |
CNHFAHCC_00514 | 7.1e-189 | rsbU | 3.1.3.3 | KT | phosphatase | |
CNHFAHCC_00515 | 7e-53 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
CNHFAHCC_00516 | 2.4e-86 | rsbW | 2.7.11.1 | F | Negative regulator of sigma-B activity. Phosphorylates and inactivates its specific antagonist protein, RsbV. Upon phosphorylation of RsbV, RsbW is released and binds to sigma-B, thereby blocking its ability to form an RNA polymerase holoenzyme (E-sigma-B) | |
CNHFAHCC_00517 | 3.4e-138 | sigB | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_00518 | 4.8e-108 | rsbX | 3.1.3.16, 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
CNHFAHCC_00522 | 1.5e-82 | ydcG | S | EVE domain | ||
CNHFAHCC_00523 | 1.6e-76 | ydcH | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_00524 | 0.0 | yhgF | K | COG2183 Transcriptional accessory protein | ||
CNHFAHCC_00525 | 1.6e-84 | ydcK | S | Belongs to the SprT family | ||
CNHFAHCC_00533 | 7e-178 | luxA | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_00534 | 2.4e-71 | lrpA | K | transcriptional | ||
CNHFAHCC_00535 | 3.9e-78 | lrpB | K | transcriptional | ||
CNHFAHCC_00536 | 9.6e-100 | yddQ | 3.5.1.19 | Q | Isochorismatase family | |
CNHFAHCC_00537 | 1.5e-143 | yddR | S | Zn-dependent hydrolases of the beta-lactamase fold | ||
CNHFAHCC_00538 | 5e-227 | ydeG | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00542 | 1.4e-112 | ydeA | 1.11.1.6, 3.5.1.124 | S | DJ-1/PfpI family | |
CNHFAHCC_00543 | 8.7e-30 | cspL | K | Cold shock | ||
CNHFAHCC_00544 | 6.1e-79 | carD | K | Transcription factor | ||
CNHFAHCC_00545 | 4.6e-35 | ydzE | EG | spore germination | ||
CNHFAHCC_00546 | 1.1e-166 | rhaS5 | K | AraC-like ligand binding domain | ||
CNHFAHCC_00547 | 2.3e-173 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
CNHFAHCC_00548 | 2.5e-166 | ydeE | K | AraC family transcriptional regulator | ||
CNHFAHCC_00549 | 2.2e-265 | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | |||
CNHFAHCC_00550 | 3.4e-220 | ydeG | EGP | Major facilitator superfamily | ||
CNHFAHCC_00551 | 2.9e-47 | ydeH | ||||
CNHFAHCC_00552 | 8.9e-107 | ydeI | S | Bacteriocin-protection, YdeI or OmpD-Associated | ||
CNHFAHCC_00553 | 4e-116 | |||||
CNHFAHCC_00554 | 1.8e-153 | ydeK | EG | -transporter | ||
CNHFAHCC_00555 | 1.5e-274 | ydeL | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
CNHFAHCC_00556 | 4.2e-74 | maoC | I | N-terminal half of MaoC dehydratase | ||
CNHFAHCC_00557 | 8.6e-107 | ydeN | S | Serine hydrolase | ||
CNHFAHCC_00558 | 1.1e-58 | K | HxlR-like helix-turn-helix | |||
CNHFAHCC_00559 | 1.9e-153 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
CNHFAHCC_00560 | 4.8e-69 | ydeP | K | Transcriptional regulator | ||
CNHFAHCC_00561 | 1e-110 | ydeQ | S | NADPH-quinone reductase (modulator of drug activity B) | ||
CNHFAHCC_00562 | 1.2e-195 | ydeR | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00563 | 6.5e-105 | ydeS | K | Transcriptional regulator | ||
CNHFAHCC_00565 | 1.3e-57 | arsR | K | transcriptional | ||
CNHFAHCC_00566 | 5.2e-232 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
CNHFAHCC_00568 | 7.2e-149 | ydfB | J | GNAT acetyltransferase | ||
CNHFAHCC_00569 | 1e-162 | ydfC | EG | EamA-like transporter family | ||
CNHFAHCC_00570 | 1.9e-275 | ydfD | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
CNHFAHCC_00571 | 5.9e-117 | ydfE | S | Flavin reductase like domain | ||
CNHFAHCC_00572 | 2.7e-123 | ydfF | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
CNHFAHCC_00573 | 1.5e-79 | ydfG | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | ||
CNHFAHCC_00575 | 5.3e-180 | ydfH | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_00576 | 1.4e-110 | ydfI | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_00577 | 0.0 | ydfJ | S | drug exporters of the RND superfamily | ||
CNHFAHCC_00578 | 1.9e-177 | S | Alpha/beta hydrolase family | |||
CNHFAHCC_00579 | 5.9e-118 | S | Protein of unknown function (DUF554) | |||
CNHFAHCC_00580 | 3.2e-147 | K | Bacterial transcription activator, effector binding domain | |||
CNHFAHCC_00581 | 1.6e-155 | fieF | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
CNHFAHCC_00582 | 9.6e-112 | ydfN | C | nitroreductase | ||
CNHFAHCC_00583 | 3.6e-187 | ydfO | E | COG0346 Lactoylglutathione lyase and related lyases | ||
CNHFAHCC_00584 | 8.8e-63 | mhqP | S | DoxX | ||
CNHFAHCC_00585 | 1.3e-57 | traF | CO | Thioredoxin | ||
CNHFAHCC_00586 | 7.1e-15 | ydgA | S | Spore germination protein gerPA/gerPF | ||
CNHFAHCC_00587 | 6.3e-29 | |||||
CNHFAHCC_00589 | 4.4e-118 | ydfR | S | Protein of unknown function (DUF421) | ||
CNHFAHCC_00590 | 5.2e-122 | ydfS | S | Protein of unknown function (DUF421) | ||
CNHFAHCC_00591 | 1.7e-75 | cotP | O | Belongs to the small heat shock protein (HSP20) family | ||
CNHFAHCC_00592 | 1.4e-37 | ydgA | S | Spore germination protein gerPA/gerPF | ||
CNHFAHCC_00593 | 1.3e-41 | ydgB | S | Spore germination protein gerPA/gerPF | ||
CNHFAHCC_00594 | 1.5e-101 | K | Bacterial regulatory proteins, tetR family | |||
CNHFAHCC_00595 | 1.9e-53 | S | DoxX-like family | |||
CNHFAHCC_00596 | 2.4e-86 | yycN | 2.3.1.128 | K | Acetyltransferase | |
CNHFAHCC_00597 | 4.2e-308 | expZ | S | ABC transporter | ||
CNHFAHCC_00598 | 4e-251 | cycA | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_00599 | 4.6e-91 | dinB | S | DinB family | ||
CNHFAHCC_00600 | 4.2e-80 | K | helix_turn_helix multiple antibiotic resistance protein | |||
CNHFAHCC_00601 | 0.0 | ydgH | S | drug exporters of the RND superfamily | ||
CNHFAHCC_00602 | 1e-113 | drgA | C | nitroreductase | ||
CNHFAHCC_00603 | 1.1e-69 | ydgJ | K | Winged helix DNA-binding domain | ||
CNHFAHCC_00604 | 2.5e-209 | tcaB | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00605 | 1.2e-121 | ydhB | S | membrane transporter protein | ||
CNHFAHCC_00606 | 6.5e-122 | ydhC | K | FCD | ||
CNHFAHCC_00607 | 3.3e-244 | ydhD | M | Glycosyl hydrolase | ||
CNHFAHCC_00608 | 7e-228 | ydhE | CG | COG1819 Glycosyl transferases, related to UDP-glucuronosyltransferase | ||
CNHFAHCC_00609 | 1.9e-127 | |||||
CNHFAHCC_00610 | 1.4e-259 | phoB | 3.1.3.1 | P | Belongs to the alkaline phosphatase family | |
CNHFAHCC_00611 | 4.6e-69 | frataxin | S | Domain of unknown function (DU1801) | ||
CNHFAHCC_00613 | 4.1e-86 | K | Acetyltransferase (GNAT) domain | |||
CNHFAHCC_00614 | 1.8e-184 | ydhJ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
CNHFAHCC_00615 | 1.7e-99 | ydhK | M | Protein of unknown function (DUF1541) | ||
CNHFAHCC_00616 | 4.6e-200 | pbuE | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00617 | 1.1e-47 | ydhM | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
CNHFAHCC_00618 | 3.5e-52 | ydhN3 | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
CNHFAHCC_00619 | 2e-239 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CNHFAHCC_00620 | 2.4e-288 | ydhP | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CNHFAHCC_00621 | 3.9e-133 | ydhQ | K | UTRA | ||
CNHFAHCC_00622 | 9.2e-172 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
CNHFAHCC_00623 | 4.2e-191 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
CNHFAHCC_00624 | 5.7e-216 | gmuG | 3.2.1.78 | GH26 | G | Belongs to the glycosyl hydrolase 26 family |
CNHFAHCC_00625 | 8.7e-78 | ydhU | P | Catalase | ||
CNHFAHCC_00626 | 1.1e-16 | ydhU | P | Manganese containing catalase | ||
CNHFAHCC_00629 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00630 | 7.8e-08 | |||||
CNHFAHCC_00632 | 4.6e-185 | thiL | 2.7.4.16 | H | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 | |
CNHFAHCC_00633 | 9.1e-86 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
CNHFAHCC_00634 | 9e-127 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
CNHFAHCC_00635 | 1.3e-84 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
CNHFAHCC_00636 | 1.2e-191 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
CNHFAHCC_00637 | 0.0 | ydiF | S | ABC transporter | ||
CNHFAHCC_00638 | 5.5e-89 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
CNHFAHCC_00639 | 8.8e-116 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
CNHFAHCC_00640 | 7.5e-22 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
CNHFAHCC_00641 | 8.4e-126 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
CNHFAHCC_00642 | 2.9e-27 | ydiK | S | Domain of unknown function (DUF4305) | ||
CNHFAHCC_00643 | 7.9e-129 | ydiL | S | CAAX protease self-immunity | ||
CNHFAHCC_00645 | 1.3e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
CNHFAHCC_00646 | 1.2e-278 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
CNHFAHCC_00647 | 1.5e-24 | S | Protein of unknown function (DUF4064) | |||
CNHFAHCC_00649 | 0.0 | K | NB-ARC domain | |||
CNHFAHCC_00650 | 3.2e-200 | gutB | 1.1.1.14 | E | Dehydrogenase | |
CNHFAHCC_00651 | 5.8e-250 | gutA | G | MFS/sugar transport protein | ||
CNHFAHCC_00652 | 4.4e-172 | ydjE | 2.7.1.4 | G | pfkB family carbohydrate kinase | |
CNHFAHCC_00653 | 4.3e-31 | yjdJ | S | Domain of unknown function (DUF4306) | ||
CNHFAHCC_00654 | 3.3e-113 | pspA | KT | Phage shock protein A | ||
CNHFAHCC_00655 | 2.6e-178 | ydjG | 3.6.4.12 | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | |
CNHFAHCC_00656 | 3.1e-120 | ydjH | S | COG1512 Beta-propeller domains of methanol dehydrogenase type | ||
CNHFAHCC_00657 | 1.1e-149 | ydjI | S | virion core protein (lumpy skin disease virus) | ||
CNHFAHCC_00658 | 0.0 | yrhL | I | Acyltransferase family | ||
CNHFAHCC_00659 | 1.4e-145 | rsiV | S | Protein of unknown function (DUF3298) | ||
CNHFAHCC_00660 | 4.3e-86 | sigV | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_00661 | 4.4e-194 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
CNHFAHCC_00662 | 7.1e-62 | ydjM | M | Lytic transglycolase | ||
CNHFAHCC_00663 | 9.4e-136 | ydjN | U | Involved in the tonB-independent uptake of proteins | ||
CNHFAHCC_00665 | 8.6e-35 | ydjO | S | Cold-inducible protein YdjO | ||
CNHFAHCC_00666 | 0.0 | cotA | 1.10.3.4, 1.16.3.3 | Q | multicopper oxidases | |
CNHFAHCC_00667 | 7.3e-245 | gabP | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_00668 | 2.2e-154 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
CNHFAHCC_00669 | 1.7e-176 | yeaC | S | COG0714 MoxR-like ATPases | ||
CNHFAHCC_00670 | 5.4e-212 | yeaD | S | conserved protein (some members contain a von Willebrand factor type A (vWA) domain) | ||
CNHFAHCC_00671 | 0.0 | yebA | E | COG1305 Transglutaminase-like enzymes | ||
CNHFAHCC_00672 | 1.2e-301 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
CNHFAHCC_00673 | 7.6e-140 | 6.3.4.18, 6.3.5.5 | F | 5-(carboxyamino)imidazole ribonucleotide synthase activity | ||
CNHFAHCC_00674 | 5.1e-117 | F | ATP-grasp domain | |||
CNHFAHCC_00675 | 1e-106 | pphA | 5.4.2.9 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
CNHFAHCC_00676 | 4.1e-135 | aspC | 2.6.1.1 | E | DegT/DnrJ/EryC1/StrS aminotransferase family | |
CNHFAHCC_00677 | 3.8e-138 | yqjV | G | Major Facilitator Superfamily | ||
CNHFAHCC_00678 | 8.6e-93 | sigV | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_00679 | 2.4e-246 | S | Domain of unknown function (DUF4179) | |||
CNHFAHCC_00680 | 6.2e-209 | pbuG | S | permease | ||
CNHFAHCC_00681 | 5.6e-133 | yebC | M | Membrane | ||
CNHFAHCC_00683 | 2e-92 | yebE | S | UPF0316 protein | ||
CNHFAHCC_00684 | 6.1e-28 | yebG | S | NETI protein | ||
CNHFAHCC_00685 | 2.5e-83 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
CNHFAHCC_00686 | 2.6e-222 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
CNHFAHCC_00687 | 3.6e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
CNHFAHCC_00688 | 1.2e-129 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
CNHFAHCC_00689 | 8.4e-38 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
CNHFAHCC_00690 | 7.3e-129 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
CNHFAHCC_00691 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
CNHFAHCC_00692 | 3.6e-271 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
CNHFAHCC_00693 | 7.6e-178 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
CNHFAHCC_00694 | 1.3e-105 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
CNHFAHCC_00695 | 1.2e-288 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
CNHFAHCC_00696 | 1.7e-235 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
CNHFAHCC_00697 | 3.5e-73 | K | helix_turn_helix ASNC type | |||
CNHFAHCC_00698 | 2.3e-232 | yjeH | E | Amino acid permease | ||
CNHFAHCC_00699 | 2.7e-27 | S | Protein of unknown function (DUF2892) | |||
CNHFAHCC_00700 | 0.0 | yerA | 3.5.4.2 | F | adenine deaminase | |
CNHFAHCC_00701 | 3e-192 | yerB | S | Protein of unknown function (DUF3048) C-terminal domain | ||
CNHFAHCC_00702 | 4.8e-51 | yerC | S | protein conserved in bacteria | ||
CNHFAHCC_00703 | 3.2e-305 | yerD | 1.4.7.1 | E | Belongs to the glutamate synthase family | |
CNHFAHCC_00705 | 2.2e-125 | pcrB | I | 35 carbon atoms) to the C3 hydroxyl of sn-glycerol-1-phosphate (G1P), producing heptaprenylglyceryl phosphate (HepGP). This reaction is an ether-bond-formation step in the biosynthesis of archaea-type G1P-based membrane lipids found in Bacillales | ||
CNHFAHCC_00706 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
CNHFAHCC_00707 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
CNHFAHCC_00708 | 4.1e-220 | camS | S | COG4851 Protein involved in sex pheromone biosynthesis | ||
CNHFAHCC_00709 | 2e-199 | yerI | S | homoserine kinase type II (protein kinase fold) | ||
CNHFAHCC_00710 | 9.4e-124 | sapB | S | MgtC SapB transporter | ||
CNHFAHCC_00711 | 2e-264 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
CNHFAHCC_00712 | 2.1e-45 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
CNHFAHCC_00713 | 1.2e-274 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
CNHFAHCC_00714 | 3.1e-270 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
CNHFAHCC_00715 | 4e-156 | yerO | K | Transcriptional regulator | ||
CNHFAHCC_00716 | 0.0 | swrC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
CNHFAHCC_00717 | 3e-170 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
CNHFAHCC_00718 | 1.2e-255 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
CNHFAHCC_00719 | 3.2e-98 | L | Recombinase | |||
CNHFAHCC_00720 | 3.2e-53 | L | Resolvase, N terminal domain | |||
CNHFAHCC_00721 | 0.0 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
CNHFAHCC_00722 | 0.0 | yeeB | L | DEAD-like helicases superfamily | ||
CNHFAHCC_00723 | 1.8e-212 | pstS | P | T5orf172 | ||
CNHFAHCC_00726 | 6.2e-31 | S | Colicin immunity protein / pyocin immunity protein | |||
CNHFAHCC_00727 | 4e-83 | S | Protein of unknown function, DUF600 | |||
CNHFAHCC_00728 | 0.0 | L | nucleic acid phosphodiester bond hydrolysis | |||
CNHFAHCC_00729 | 1.8e-192 | 3.4.24.40 | CO | amine dehydrogenase activity | ||
CNHFAHCC_00730 | 5.5e-214 | S | Tetratricopeptide repeat | |||
CNHFAHCC_00732 | 9.4e-127 | yeeN | K | transcriptional regulatory protein | ||
CNHFAHCC_00734 | 1.2e-103 | dhaR3 | K | Transcriptional regulator | ||
CNHFAHCC_00735 | 9.7e-82 | yesE | S | SnoaL-like domain | ||
CNHFAHCC_00736 | 2.2e-159 | yesF | GM | NAD(P)H-binding | ||
CNHFAHCC_00737 | 5.3e-45 | cotJA | S | Spore coat associated protein JA (CotJA) | ||
CNHFAHCC_00738 | 1.5e-45 | cotJB | S | CotJB protein | ||
CNHFAHCC_00739 | 5.2e-104 | cotJC | P | Spore Coat | ||
CNHFAHCC_00740 | 4.2e-103 | yesJ | K | Acetyltransferase (GNAT) family | ||
CNHFAHCC_00742 | 4.4e-104 | yesL | S | Protein of unknown function, DUF624 | ||
CNHFAHCC_00743 | 0.0 | yesM | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_00744 | 2.9e-204 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
CNHFAHCC_00745 | 5e-248 | yesO | G | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_00746 | 6.9e-167 | yesP | G | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_00747 | 1.3e-165 | yesQ | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_00748 | 1.6e-199 | 3.2.1.172 | GH105 | S | Glycosyl Hydrolase Family 88 | |
CNHFAHCC_00749 | 0.0 | yesS | K | Transcriptional regulator | ||
CNHFAHCC_00750 | 3.8e-133 | E | GDSL-like Lipase/Acylhydrolase | |||
CNHFAHCC_00751 | 8.9e-132 | yesU | S | Domain of unknown function (DUF1961) | ||
CNHFAHCC_00752 | 1e-113 | yesV | S | Protein of unknown function, DUF624 | ||
CNHFAHCC_00753 | 0.0 | yesX | 4.2.2.23, 4.2.2.24 | PL11 | E | cell wall organization |
CNHFAHCC_00754 | 0.0 | yesX | 4.2.2.23, 4.2.2.24 | PL11 | E | cell wall organization |
CNHFAHCC_00755 | 3e-124 | yesY | E | GDSL-like Lipase/Acylhydrolase | ||
CNHFAHCC_00756 | 0.0 | yesZ | 3.2.1.23 | G | beta-galactosidase activity | |
CNHFAHCC_00757 | 0.0 | yetA | ||||
CNHFAHCC_00758 | 9.6e-291 | lplA | G | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_00759 | 1.3e-176 | lplB | G | COG4209 ABC-type polysaccharide transport system, permease component | ||
CNHFAHCC_00760 | 1.7e-162 | lplC | G | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_00761 | 3.3e-258 | lplD | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase |
CNHFAHCC_00762 | 6.1e-123 | yetF | S | membrane | ||
CNHFAHCC_00763 | 4.4e-55 | isdI | 1.14.99.48, 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | |
CNHFAHCC_00764 | 2e-64 | yetH | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
CNHFAHCC_00765 | 2.2e-34 | |||||
CNHFAHCC_00766 | 2.2e-89 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
CNHFAHCC_00767 | 4.4e-43 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
CNHFAHCC_00768 | 8.9e-20 | yezD | S | Uncharacterized small protein (DUF2292) | ||
CNHFAHCC_00769 | 5.3e-105 | yetJ | S | Belongs to the BI1 family | ||
CNHFAHCC_00770 | 1.3e-171 | yetK | EG | EamA-like transporter family | ||
CNHFAHCC_00771 | 6.4e-90 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_00772 | 7.8e-213 | yetM | CH | FAD binding domain | ||
CNHFAHCC_00773 | 3.6e-199 | yetN | S | Protein of unknown function (DUF3900) | ||
CNHFAHCC_00774 | 0.0 | cypD | 1.14.14.1, 1.6.2.4 | C | Belongs to the cytochrome P450 family | |
CNHFAHCC_00775 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
CNHFAHCC_00776 | 2.1e-148 | rfbF | 2.7.7.33 | JM | Nucleotidyl transferase | |
CNHFAHCC_00777 | 1.9e-172 | yfnG | 4.2.1.45 | M | dehydratase | |
CNHFAHCC_00778 | 3.8e-181 | yfnF | M | Nucleotide-diphospho-sugar transferase | ||
CNHFAHCC_00779 | 1.4e-225 | yfnE | 2.4.1.338 | GT2 | S | Glycosyltransferase like family 2 |
CNHFAHCC_00780 | 1.8e-180 | yfnD | M | Nucleotide-diphospho-sugar transferase | ||
CNHFAHCC_00781 | 2e-206 | fsr | P | COG0477 Permeases of the major facilitator superfamily | ||
CNHFAHCC_00782 | 7.8e-134 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
CNHFAHCC_00783 | 1.3e-241 | yfnA | E | amino acid | ||
CNHFAHCC_00784 | 2.8e-279 | yfmT | 1.2.1.3, 1.2.1.67 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
CNHFAHCC_00785 | 1.1e-113 | yfmS | NT | chemotaxis protein | ||
CNHFAHCC_00786 | 0.0 | yfmR | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
CNHFAHCC_00787 | 3e-75 | yfmQ | S | Uncharacterised protein from bacillus cereus group | ||
CNHFAHCC_00788 | 8.5e-77 | yfmP | K | transcriptional | ||
CNHFAHCC_00789 | 1.5e-209 | yfmO | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00790 | 1.4e-19 | |||||
CNHFAHCC_00791 | 1.9e-297 | yfmM | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
CNHFAHCC_00792 | 6.3e-202 | yfmL | 3.6.4.13 | L | COG0513 Superfamily II DNA and RNA helicases | |
CNHFAHCC_00793 | 7.5e-82 | yfmK | 2.3.1.128 | K | acetyltransferase | |
CNHFAHCC_00794 | 8.5e-190 | yfmJ | S | N-terminal domain of oxidoreductase | ||
CNHFAHCC_00795 | 7.7e-214 | G | Major Facilitator Superfamily | |||
CNHFAHCC_00796 | 2.6e-296 | 1.14.99.50 | S | Sulfatase-modifying factor enzyme 1 | ||
CNHFAHCC_00797 | 1.1e-149 | yfmF | 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
CNHFAHCC_00798 | 1.2e-169 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00799 | 4.4e-165 | viuD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00800 | 3.4e-169 | fecB | P | COG4594 ABC-type Fe3 -citrate transport system, periplasmic component | ||
CNHFAHCC_00801 | 2.6e-24 | S | Protein of unknown function (DUF3212) | |||
CNHFAHCC_00802 | 7.6e-58 | yflT | S | Heat induced stress protein YflT | ||
CNHFAHCC_00803 | 3.8e-240 | pel | 4.2.2.10, 4.2.2.2 | G | Pectate lyase | |
CNHFAHCC_00804 | 3.2e-235 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
CNHFAHCC_00805 | 1e-290 | citS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
CNHFAHCC_00806 | 8.9e-119 | citT | T | response regulator | ||
CNHFAHCC_00807 | 3e-181 | yflP | S | Tripartite tricarboxylate transporter family receptor | ||
CNHFAHCC_00809 | 8.5e-227 | citM | C | Citrate transporter | ||
CNHFAHCC_00810 | 5.5e-152 | yflN | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
CNHFAHCC_00811 | 1.3e-217 | nos | 1.14.14.47 | C | Belongs to the NOS family. Bacterial NOS oxygenase subfamily | |
CNHFAHCC_00812 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
CNHFAHCC_00813 | 9e-124 | yflK | S | protein conserved in bacteria | ||
CNHFAHCC_00814 | 4e-18 | yflJ | S | Protein of unknown function (DUF2639) | ||
CNHFAHCC_00815 | 4.1e-19 | yflI | ||||
CNHFAHCC_00816 | 2.4e-50 | yflH | S | Protein of unknown function (DUF3243) | ||
CNHFAHCC_00817 | 1.1e-138 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
CNHFAHCC_00818 | 1.1e-250 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | COG1263 Phosphotransferase system IIC components, glucose maltose N-acetylglucosamine-specific | |
CNHFAHCC_00819 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
CNHFAHCC_00820 | 6e-67 | yhdN | S | Domain of unknown function (DUF1992) | ||
CNHFAHCC_00821 | 3.4e-256 | agcS_1 | E | Sodium alanine symporter | ||
CNHFAHCC_00822 | 1.6e-194 | E | Spore germination protein | |||
CNHFAHCC_00824 | 5.1e-207 | yfkR | S | spore germination | ||
CNHFAHCC_00825 | 1.5e-283 | yfkQ | EG | Spore germination protein | ||
CNHFAHCC_00826 | 8.5e-257 | treP | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_00827 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
CNHFAHCC_00828 | 1.8e-133 | treR | K | transcriptional | ||
CNHFAHCC_00829 | 1.6e-125 | yfkO | C | nitroreductase | ||
CNHFAHCC_00830 | 0.0 | cpdB | 3.1.3.5, 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
CNHFAHCC_00831 | 1.6e-91 | yfkM | 1.11.1.6, 3.5.1.124 | S | protease | |
CNHFAHCC_00832 | 6.8e-207 | ydiM | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00833 | 2.1e-29 | yfkK | S | Belongs to the UPF0435 family | ||
CNHFAHCC_00834 | 2.2e-84 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
CNHFAHCC_00835 | 8.4e-51 | yfkI | S | gas vesicle protein | ||
CNHFAHCC_00836 | 9.7e-144 | yihY | S | Belongs to the UPF0761 family | ||
CNHFAHCC_00837 | 2.9e-08 | |||||
CNHFAHCC_00838 | 6.9e-220 | ycaD | EGP | COG0477 Permeases of the major facilitator superfamily | ||
CNHFAHCC_00839 | 6.1e-183 | cax | P | COG0387 Ca2 H antiporter | ||
CNHFAHCC_00840 | 1.2e-146 | yfkD | S | YfkD-like protein | ||
CNHFAHCC_00841 | 6e-149 | yfkC | M | Mechanosensitive ion channel | ||
CNHFAHCC_00842 | 5.4e-222 | yfkA | S | YfkB-like domain | ||
CNHFAHCC_00843 | 1.1e-26 | yfjT | ||||
CNHFAHCC_00844 | 2.6e-154 | pdaA | G | deacetylase | ||
CNHFAHCC_00845 | 4.2e-150 | yfjR | 1.1.1.31 | I | NAD-binding of NADP-dependent 3-hydroxyisobutyrate dehydrogenase | |
CNHFAHCC_00846 | 3.8e-184 | corA | P | Mediates influx of magnesium ions | ||
CNHFAHCC_00847 | 1e-167 | yfjP | 3.2.2.21 | L | COG0122 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
CNHFAHCC_00848 | 1.1e-267 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
CNHFAHCC_00849 | 1.6e-39 | S | YfzA-like protein | |||
CNHFAHCC_00850 | 5.1e-192 | yfjN | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
CNHFAHCC_00851 | 3.9e-86 | yfjM | S | Psort location Cytoplasmic, score | ||
CNHFAHCC_00852 | 3e-29 | yfjL | ||||
CNHFAHCC_00853 | 1.2e-191 | acoA | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | ||
CNHFAHCC_00854 | 1e-190 | acoB | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | ||
CNHFAHCC_00855 | 2.9e-197 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
CNHFAHCC_00856 | 6.4e-257 | acoL | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
CNHFAHCC_00857 | 0.0 | acoR | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | ||
CNHFAHCC_00858 | 1.2e-25 | sspH | S | Belongs to the SspH family | ||
CNHFAHCC_00859 | 4e-56 | yfjF | S | UPF0060 membrane protein | ||
CNHFAHCC_00860 | 1.3e-80 | S | Family of unknown function (DUF5381) | |||
CNHFAHCC_00861 | 1.8e-101 | yfjD | S | Family of unknown function (DUF5381) | ||
CNHFAHCC_00862 | 4.1e-144 | yfjC | ||||
CNHFAHCC_00863 | 9.2e-191 | yfjB | ||||
CNHFAHCC_00864 | 1.2e-44 | yfjA | S | Belongs to the WXG100 family | ||
CNHFAHCC_00865 | 9.9e-263 | aglB | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
CNHFAHCC_00866 | 3.2e-141 | glvR | K | Helix-turn-helix domain, rpiR family | ||
CNHFAHCC_00867 | 4.7e-296 | glvC | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_00868 | 2.1e-310 | yfiB3 | V | ABC transporter | ||
CNHFAHCC_00869 | 0.0 | yfiC | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
CNHFAHCC_00870 | 9.8e-65 | mhqP | S | DoxX | ||
CNHFAHCC_00871 | 5.7e-163 | yfiE | 1.13.11.2 | S | glyoxalase | |
CNHFAHCC_00872 | 1.5e-177 | K | AraC-like ligand binding domain | |||
CNHFAHCC_00873 | 1.8e-262 | iolT | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00874 | 8.4e-184 | G | Xylose isomerase | |||
CNHFAHCC_00875 | 3.8e-234 | S | Oxidoreductase | |||
CNHFAHCC_00877 | 1.1e-214 | yxjM | T | Histidine kinase | ||
CNHFAHCC_00878 | 3.2e-113 | KT | LuxR family transcriptional regulator | |||
CNHFAHCC_00879 | 6.2e-171 | V | ABC transporter, ATP-binding protein | |||
CNHFAHCC_00880 | 9.8e-214 | V | ABC-2 family transporter protein | |||
CNHFAHCC_00881 | 4.6e-208 | V | COG0842 ABC-type multidrug transport system, permease component | |||
CNHFAHCC_00882 | 8.3e-99 | padR | K | transcriptional | ||
CNHFAHCC_00883 | 3.1e-78 | estA | 3.1.1.3 | S | acetyltransferases and hydrolases with the alpha beta hydrolase fold | |
CNHFAHCC_00884 | 9e-198 | yfiQ | G | COG3936 Protein involved in polysaccharide intercellular adhesin (PIA) synthesis biofilm formation | ||
CNHFAHCC_00885 | 2e-109 | yfiR | K | Transcriptional regulator | ||
CNHFAHCC_00886 | 5.1e-221 | yfiS | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00887 | 3.3e-100 | yfiT | S | Belongs to the metal hydrolase YfiT family | ||
CNHFAHCC_00888 | 8.7e-287 | yfiU | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00889 | 3.1e-81 | yfiV | K | transcriptional | ||
CNHFAHCC_00890 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
CNHFAHCC_00891 | 6.2e-182 | yfiY | P | ABC transporter substrate-binding protein | ||
CNHFAHCC_00892 | 3.1e-176 | yfiZ | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00893 | 5.2e-171 | yfhA | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_00894 | 1.8e-167 | yfhB | 5.3.3.17 | S | PhzF family | |
CNHFAHCC_00895 | 3.9e-107 | yfhC | C | nitroreductase | ||
CNHFAHCC_00896 | 2.1e-25 | yfhD | S | YfhD-like protein | ||
CNHFAHCC_00898 | 4.9e-173 | yfhF | S | nucleoside-diphosphate sugar epimerase | ||
CNHFAHCC_00899 | 1.1e-141 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
CNHFAHCC_00900 | 9.7e-52 | yfhH | S | Protein of unknown function (DUF1811) | ||
CNHFAHCC_00901 | 1.1e-209 | yfhI | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00902 | 6.2e-20 | sspK | S | reproduction | ||
CNHFAHCC_00903 | 1.3e-44 | yfhJ | S | WVELL protein | ||
CNHFAHCC_00904 | 9.2e-92 | batE | T | Bacterial SH3 domain homologues | ||
CNHFAHCC_00905 | 8.7e-51 | yfhL | S | SdpI/YhfL protein family | ||
CNHFAHCC_00906 | 6.7e-172 | yfhM | S | Alpha beta hydrolase | ||
CNHFAHCC_00907 | 2.7e-185 | csbB | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
CNHFAHCC_00908 | 0.0 | yfhO | S | Bacterial membrane protein YfhO | ||
CNHFAHCC_00909 | 5.5e-186 | yfhP | S | membrane-bound metal-dependent | ||
CNHFAHCC_00910 | 7e-212 | mutY | L | A G-specific | ||
CNHFAHCC_00911 | 6.9e-36 | yfhS | ||||
CNHFAHCC_00912 | 2.9e-134 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_00913 | 2.4e-08 | sspE | S | Small, acid-soluble spore protein, gamma-type | ||
CNHFAHCC_00914 | 1.5e-37 | ygaB | S | YgaB-like protein | ||
CNHFAHCC_00915 | 1.3e-104 | ygaC | J | Belongs to the UPF0374 family | ||
CNHFAHCC_00916 | 1.8e-301 | ygaD | V | ABC transporter | ||
CNHFAHCC_00917 | 1.4e-179 | ygaE | S | Membrane | ||
CNHFAHCC_00918 | 1.2e-246 | gsaB | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
CNHFAHCC_00919 | 2.8e-87 | bcp | 1.11.1.15 | O | Peroxiredoxin | |
CNHFAHCC_00920 | 4e-80 | perR | P | Belongs to the Fur family | ||
CNHFAHCC_00921 | 1.5e-56 | ygzB | S | UPF0295 protein | ||
CNHFAHCC_00922 | 6.7e-167 | ygxA | S | Nucleotidyltransferase-like | ||
CNHFAHCC_00923 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_00928 | 7.8e-08 | |||||
CNHFAHCC_00936 | 2e-08 | |||||
CNHFAHCC_00940 | 2.7e-143 | spo0M | S | COG4326 Sporulation control protein | ||
CNHFAHCC_00941 | 3e-27 | |||||
CNHFAHCC_00942 | 7.2e-134 | pepE | 3.4.11.2, 3.4.13.21 | E | Belongs to the peptidase S51 family | |
CNHFAHCC_00944 | 0.0 | thiC | 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
CNHFAHCC_00945 | 1.9e-266 | ygaK | C | Berberine and berberine like | ||
CNHFAHCC_00947 | 3.2e-291 | katA | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
CNHFAHCC_00948 | 1.1e-145 | ssuB | P | COG1116 ABC-type nitrate sulfonate bicarbonate transport system, ATPase component | ||
CNHFAHCC_00949 | 1.7e-171 | ssuA | M | Sulfonate ABC transporter | ||
CNHFAHCC_00950 | 1.5e-147 | ssuC | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
CNHFAHCC_00951 | 3.1e-217 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
CNHFAHCC_00953 | 6e-42 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
CNHFAHCC_00954 | 4.1e-78 | ygaO | ||||
CNHFAHCC_00955 | 4.4e-29 | K | Transcriptional regulator | |||
CNHFAHCC_00957 | 7.9e-114 | yhzB | S | B3/4 domain | ||
CNHFAHCC_00958 | 2.1e-224 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
CNHFAHCC_00959 | 9.5e-180 | yhbB | S | Putative amidase domain | ||
CNHFAHCC_00960 | 8.2e-87 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
CNHFAHCC_00961 | 1.2e-109 | yhbD | K | Protein of unknown function (DUF4004) | ||
CNHFAHCC_00962 | 1.6e-65 | yhbE | M | COG1664 Integral membrane protein CcmA involved in cell shape determination | ||
CNHFAHCC_00963 | 8.2e-75 | yhbF | M | COG1664 Integral membrane protein CcmA involved in cell shape determination | ||
CNHFAHCC_00964 | 0.0 | prkA | T | Ser protein kinase | ||
CNHFAHCC_00965 | 2.5e-225 | yhbH | S | Belongs to the UPF0229 family | ||
CNHFAHCC_00966 | 2.2e-76 | yhbI | K | DNA-binding transcription factor activity | ||
CNHFAHCC_00967 | 3.1e-97 | yhbJ | V | COG1566 Multidrug resistance efflux pump | ||
CNHFAHCC_00968 | 3.1e-271 | yhcA | EGP | Major facilitator Superfamily | ||
CNHFAHCC_00969 | 1e-98 | yhcB | 1.6.5.2 | S | Belongs to the WrbA family | |
CNHFAHCC_00970 | 2.8e-37 | yhcC | ||||
CNHFAHCC_00971 | 7.8e-55 | |||||
CNHFAHCC_00972 | 6.6e-60 | yhcF | K | Transcriptional regulator | ||
CNHFAHCC_00973 | 1.6e-123 | yhcG | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_00974 | 2.6e-166 | yhcH | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_00975 | 3.9e-165 | yhcI | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | ||
CNHFAHCC_00976 | 1e-30 | cspB | K | Cold-shock protein | ||
CNHFAHCC_00977 | 5.2e-153 | metQ | M | Belongs to the nlpA lipoprotein family | ||
CNHFAHCC_00978 | 1.2e-197 | yhcK | 2.7.7.65 | T | COG2199 FOG GGDEF domain | |
CNHFAHCC_00979 | 6.3e-220 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
CNHFAHCC_00980 | 3.7e-44 | yhcM | ||||
CNHFAHCC_00981 | 2.1e-68 | yhcN | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
CNHFAHCC_00982 | 2.5e-167 | yhcP | ||||
CNHFAHCC_00983 | 5.2e-100 | yhcQ | M | Spore coat protein | ||
CNHFAHCC_00984 | 0.0 | yhcR | 3.1.3.5, 3.1.31.1 | F | Belongs to the 5'-nucleotidase family | |
CNHFAHCC_00985 | 7.6e-106 | yhcS | 3.4.22.70 | M | COG3764 Sortase (surface protein transpeptidase) | |
CNHFAHCC_00986 | 7.9e-171 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
CNHFAHCC_00987 | 9.3e-68 | yhcU | S | Family of unknown function (DUF5365) | ||
CNHFAHCC_00988 | 9.9e-68 | yhcV | S | COG0517 FOG CBS domain | ||
CNHFAHCC_00989 | 4.6e-120 | yhcW | 5.4.2.6 | S | hydrolase | |
CNHFAHCC_00990 | 2.7e-304 | yhcX | 3.5.1.3 | K | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
CNHFAHCC_00991 | 1.1e-261 | yhxA | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | ||
CNHFAHCC_00992 | 5.2e-104 | glpP | K | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | ||
CNHFAHCC_00993 | 1.9e-152 | glpF | G | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
CNHFAHCC_00994 | 4.6e-293 | glpK | 2.7.1.30 | C | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
CNHFAHCC_00995 | 0.0 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
CNHFAHCC_00996 | 0.0 | pmmB | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
CNHFAHCC_00997 | 6.7e-212 | yhcY | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_00998 | 1.1e-113 | yhcZ | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_00999 | 1.4e-84 | azr | 1.7.1.6 | S | NADPH-dependent FMN reductase | |
CNHFAHCC_01000 | 1.2e-38 | yhdB | S | YhdB-like protein | ||
CNHFAHCC_01001 | 4.8e-54 | yhdC | S | Protein of unknown function (DUF3889) | ||
CNHFAHCC_01002 | 7.9e-189 | cwlS | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
CNHFAHCC_01003 | 3.5e-76 | nsrR | K | Transcriptional regulator | ||
CNHFAHCC_01004 | 8.7e-239 | ygxB | M | Conserved TM helix | ||
CNHFAHCC_01005 | 2.1e-276 | ycgB | S | Stage V sporulation protein R | ||
CNHFAHCC_01006 | 5.8e-258 | phoB | 3.1.3.1 | P | Belongs to the alkaline phosphatase family | |
CNHFAHCC_01007 | 2.5e-141 | lytE | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
CNHFAHCC_01008 | 3.8e-162 | citR | K | Transcriptional regulator | ||
CNHFAHCC_01009 | 1.4e-206 | citA | 2.3.3.1 | C | Belongs to the citrate synthase family | |
CNHFAHCC_01010 | 4.9e-162 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_01011 | 3.4e-250 | yhdG | E | amino acid | ||
CNHFAHCC_01012 | 1.5e-242 | yhdH | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
CNHFAHCC_01013 | 3.7e-276 | ydeL | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
CNHFAHCC_01014 | 7.5e-77 | BH1582 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
CNHFAHCC_01015 | 8.1e-45 | yhdK | S | Sigma-M inhibitor protein | ||
CNHFAHCC_01016 | 6.6e-201 | yhdL | S | Sigma factor regulator N-terminal | ||
CNHFAHCC_01017 | 5.5e-86 | sigM | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_01018 | 1.5e-191 | yhdN | C | Aldo keto reductase | ||
CNHFAHCC_01019 | 3e-110 | plsC | 2.3.1.51 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
CNHFAHCC_01020 | 3.1e-240 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
CNHFAHCC_01021 | 4.1e-74 | cueR | K | transcriptional | ||
CNHFAHCC_01022 | 1.4e-223 | yhdR | 2.6.1.1 | E | Aminotransferase | |
CNHFAHCC_01023 | 1.1e-240 | corC1 | P | COG1253 Hemolysins and related proteins containing CBS domains | ||
CNHFAHCC_01024 | 2.8e-47 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
CNHFAHCC_01025 | 5.1e-66 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
CNHFAHCC_01026 | 3.3e-135 | yhdW | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
CNHFAHCC_01028 | 6.6e-204 | yhdY | M | Mechanosensitive ion channel | ||
CNHFAHCC_01029 | 1.2e-140 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
CNHFAHCC_01030 | 1.7e-151 | yheN | G | deacetylase | ||
CNHFAHCC_01031 | 1.1e-153 | dat | 2.6.1.21 | E | Acts on the D-isomers of alanine, leucine, aspartate, glutamate, aminobutyrate, norvaline and asparagine. The enzyme transfers an amino group from a substrate D-amino acid to the pyridoxal phosphate cofactor to form pyridoxamine and an alpha- keto acid in the first half-reaction | |
CNHFAHCC_01032 | 2.2e-233 | nhaC | C | Na H antiporter | ||
CNHFAHCC_01033 | 3.1e-84 | nhaX | T | Belongs to the universal stress protein A family | ||
CNHFAHCC_01034 | 0.0 | yheI | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
CNHFAHCC_01035 | 0.0 | yheH | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
CNHFAHCC_01036 | 3.7e-111 | yheG | GM | NAD(P)H-binding | ||
CNHFAHCC_01037 | 6.3e-28 | sspB | S | spore protein | ||
CNHFAHCC_01038 | 1.3e-36 | yheE | S | Family of unknown function (DUF5342) | ||
CNHFAHCC_01039 | 1.6e-268 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
CNHFAHCC_01040 | 4.3e-216 | yheC | HJ | YheC/D like ATP-grasp | ||
CNHFAHCC_01041 | 6.7e-204 | yheB | S | Belongs to the UPF0754 family | ||
CNHFAHCC_01042 | 9.5e-48 | yheA | S | Belongs to the UPF0342 family | ||
CNHFAHCC_01043 | 3.1e-206 | yhaZ | L | DNA alkylation repair enzyme | ||
CNHFAHCC_01044 | 4.3e-142 | yhaX | S | haloacid dehalogenase-like hydrolase | ||
CNHFAHCC_01045 | 9.3e-294 | hemZ | H | coproporphyrinogen III oxidase | ||
CNHFAHCC_01046 | 1.7e-208 | yhaU | P | COG0475 Kef-type K transport systems, membrane components | ||
CNHFAHCC_01047 | 7.8e-88 | yhaT | P | regulatory, ligand-binding protein related to C-terminal domains of K channels | ||
CNHFAHCC_01049 | 1.9e-133 | yhaR | 5.3.3.18 | I | enoyl-CoA hydratase | |
CNHFAHCC_01050 | 1.1e-26 | S | YhzD-like protein | |||
CNHFAHCC_01051 | 1.8e-167 | yhaQ | S | ABC transporter, ATP-binding protein | ||
CNHFAHCC_01052 | 4.2e-215 | yhaP | CP | COG1668 ABC-type Na efflux pump, permease component | ||
CNHFAHCC_01053 | 9.4e-228 | yhaO | L | DNA repair exonuclease | ||
CNHFAHCC_01054 | 0.0 | yhaN | L | AAA domain | ||
CNHFAHCC_01055 | 1.5e-177 | yhaM | L | Shows a 3'-5' exoribonuclease activity | ||
CNHFAHCC_01056 | 1.6e-21 | yhaL | S | Sporulation protein YhaL | ||
CNHFAHCC_01057 | 1.9e-121 | prsA | 5.2.1.8 | M | plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
CNHFAHCC_01058 | 8.7e-90 | yhaK | S | Putative zincin peptidase | ||
CNHFAHCC_01059 | 1.3e-54 | yhaI | S | Protein of unknown function (DUF1878) | ||
CNHFAHCC_01060 | 1e-113 | hpr | K | Negative regulator of protease production and sporulation | ||
CNHFAHCC_01061 | 7e-39 | yhaH | S | YtxH-like protein | ||
CNHFAHCC_01062 | 3.6e-80 | trpP | S | Tryptophan transporter TrpP | ||
CNHFAHCC_01063 | 9.9e-205 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
CNHFAHCC_01064 | 4.7e-81 | hit | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
CNHFAHCC_01065 | 4.6e-137 | ecsA | V | transporter (ATP-binding protein) | ||
CNHFAHCC_01066 | 1.8e-215 | ecsB | U | ABC transporter | ||
CNHFAHCC_01067 | 4.8e-115 | ecsC | S | EcsC protein family | ||
CNHFAHCC_01068 | 2.3e-231 | yhaA | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
CNHFAHCC_01069 | 1.9e-248 | yhfA | C | membrane | ||
CNHFAHCC_01070 | 5.4e-10 | 1.15.1.2 | C | Rubrerythrin | ||
CNHFAHCC_01071 | 1.3e-90 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
CNHFAHCC_01072 | 0.0 | pbpF | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
CNHFAHCC_01073 | 1.7e-204 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
CNHFAHCC_01074 | 1.5e-177 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
CNHFAHCC_01075 | 1.7e-268 | hemG | 1.14.19.9, 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
CNHFAHCC_01076 | 1.4e-101 | yhgD | K | Transcriptional regulator | ||
CNHFAHCC_01077 | 1e-238 | yhgE | S | YhgE Pip N-terminal domain protein | ||
CNHFAHCC_01078 | 3e-184 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
CNHFAHCC_01079 | 9.8e-138 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
CNHFAHCC_01081 | 1.6e-199 | yhfE | 3.2.1.4 | GH5,GH9 | G | peptidase M42 |
CNHFAHCC_01082 | 1.7e-72 | 3.4.13.21 | S | ASCH | ||
CNHFAHCC_01083 | 3.8e-227 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
CNHFAHCC_01084 | 1.8e-141 | yhfI | S | COG1234 Metal-dependent hydrolases of the beta-lactamase superfamily III | ||
CNHFAHCC_01085 | 2e-191 | lplJ | 6.3.1.20 | H | Lipoate-protein ligase | |
CNHFAHCC_01086 | 2.6e-112 | yhfK | GM | NmrA-like family | ||
CNHFAHCC_01087 | 7.3e-302 | fadD | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
CNHFAHCC_01088 | 1.9e-65 | yhfM | ||||
CNHFAHCC_01089 | 5.4e-242 | yhfN | 3.4.24.84 | O | Peptidase M48 | |
CNHFAHCC_01090 | 2.3e-204 | aprE | 3.4.21.62 | O | Belongs to the peptidase S8 family | |
CNHFAHCC_01091 | 9.2e-80 | VY92_01935 | K | acetyltransferase | ||
CNHFAHCC_01092 | 8.3e-182 | yhfP | 1.1.1.1 | C | Quinone oxidoreductase | |
CNHFAHCC_01093 | 4.3e-159 | yfmC | M | Periplasmic binding protein | ||
CNHFAHCC_01094 | 1.9e-109 | yhfR | 3.1.3.73 | G | Belongs to the phosphoglycerate mutase family | |
CNHFAHCC_01095 | 2.3e-201 | vraB | 2.3.1.9 | I | Belongs to the thiolase family | |
CNHFAHCC_01096 | 1e-281 | yhfT | 6.2.1.3 | IQ | AMP-binding enzyme C-terminal domain | |
CNHFAHCC_01097 | 5e-91 | bioY | S | BioY family | ||
CNHFAHCC_01098 | 1e-182 | hemAT | NT | chemotaxis protein | ||
CNHFAHCC_01099 | 1.2e-302 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
CNHFAHCC_01100 | 1.6e-157 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_01101 | 1.3e-32 | yhzC | S | IDEAL | ||
CNHFAHCC_01102 | 4.2e-109 | comK | K | Competence transcription factor | ||
CNHFAHCC_01103 | 2.1e-168 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_01104 | 7.8e-42 | yhjA | S | Excalibur calcium-binding domain | ||
CNHFAHCC_01105 | 6.1e-266 | yhjB | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
CNHFAHCC_01106 | 6.9e-27 | yhjC | S | Protein of unknown function (DUF3311) | ||
CNHFAHCC_01107 | 5e-60 | yhjD | ||||
CNHFAHCC_01108 | 9.1e-110 | yhjE | S | SNARE associated Golgi protein | ||
CNHFAHCC_01109 | 1.2e-91 | sipV | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CNHFAHCC_01110 | 1.1e-286 | yhjG | CH | FAD binding domain | ||
CNHFAHCC_01111 | 1.2e-94 | yhjH | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_01112 | 6.9e-215 | glcP | G | Major Facilitator Superfamily | ||
CNHFAHCC_01113 | 1.1e-200 | thuB | 1.1.1.361 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
CNHFAHCC_01114 | 1.8e-161 | ntdB | 3.1.3.92 | S | Sucrose-6F-phosphate phosphohydrolase | |
CNHFAHCC_01115 | 4.4e-255 | ntdA | 2.6.1.104 | E | Belongs to the DegT DnrJ EryC1 family | |
CNHFAHCC_01116 | 7e-189 | yhjM | 5.1.1.1 | K | Transcriptional regulator | |
CNHFAHCC_01117 | 3.8e-202 | abrB | S | membrane | ||
CNHFAHCC_01118 | 3.1e-215 | EGP | Transmembrane secretion effector | |||
CNHFAHCC_01119 | 0.0 | S | Sugar transport-related sRNA regulator N-term | |||
CNHFAHCC_01120 | 2e-36 | yhjQ | C | COG1145 Ferredoxin | ||
CNHFAHCC_01121 | 2.2e-78 | yhjR | S | Rubrerythrin | ||
CNHFAHCC_01122 | 0.0 | addB | 3.1.21.3, 3.6.4.12 | L | ATP-dependent helicase deoxyribonuclease subunit B | |
CNHFAHCC_01123 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
CNHFAHCC_01124 | 1.7e-221 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
CNHFAHCC_01125 | 0.0 | sbcC | L | COG0419 ATPase involved in DNA repair | ||
CNHFAHCC_01126 | 6e-51 | yisB | V | COG1403 Restriction endonuclease | ||
CNHFAHCC_01127 | 4.5e-32 | gerPF | S | Spore germination protein gerPA/gerPF | ||
CNHFAHCC_01128 | 3e-66 | gerPE | S | Spore germination protein GerPE | ||
CNHFAHCC_01129 | 6.3e-24 | gerPD | S | Spore germination protein | ||
CNHFAHCC_01130 | 1.8e-54 | gerPC | S | Spore germination protein | ||
CNHFAHCC_01131 | 4e-34 | gerPB | S | cell differentiation | ||
CNHFAHCC_01132 | 1.9e-33 | gerPA | S | Spore germination protein | ||
CNHFAHCC_01133 | 1.5e-22 | yisI | S | Spo0E like sporulation regulatory protein | ||
CNHFAHCC_01134 | 1.7e-176 | cotH | M | Spore Coat | ||
CNHFAHCC_01135 | 3.2e-172 | yisK | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
CNHFAHCC_01136 | 3e-57 | yisL | S | UPF0344 protein | ||
CNHFAHCC_01137 | 0.0 | wprA | O | Belongs to the peptidase S8 family | ||
CNHFAHCC_01138 | 7.2e-106 | yisN | S | Protein of unknown function (DUF2777) | ||
CNHFAHCC_01139 | 0.0 | asnO | 6.3.5.4 | E | Asparagine synthase | |
CNHFAHCC_01140 | 2.1e-88 | yizA | S | Damage-inducible protein DinB | ||
CNHFAHCC_01141 | 6.8e-150 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | phytoene | |
CNHFAHCC_01142 | 4e-243 | yisQ | V | Mate efflux family protein | ||
CNHFAHCC_01143 | 1.4e-161 | yisR | K | Transcriptional regulator | ||
CNHFAHCC_01144 | 2.4e-184 | purR | K | helix_turn _helix lactose operon repressor | ||
CNHFAHCC_01145 | 4.5e-199 | yisS | 1.1.1.370 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
CNHFAHCC_01146 | 1.3e-93 | yisT | S | DinB family | ||
CNHFAHCC_01147 | 6.4e-108 | argO | S | Lysine exporter protein LysE YggA | ||
CNHFAHCC_01148 | 1.2e-282 | yisV | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
CNHFAHCC_01149 | 4e-36 | mcbG | S | Pentapeptide repeats (9 copies) | ||
CNHFAHCC_01150 | 3.1e-155 | yisY | I | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | ||
CNHFAHCC_01151 | 4.9e-113 | cysC | 1.8.4.10, 1.8.4.8, 2.7.1.25, 2.7.7.4 | P | Catalyzes the synthesis of activated sulfate | |
CNHFAHCC_01152 | 3.2e-233 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
CNHFAHCC_01153 | 6.7e-135 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
CNHFAHCC_01154 | 4.9e-125 | comB | 3.1.3.71 | H | Belongs to the ComB family | |
CNHFAHCC_01155 | 1.9e-141 | yitD | 4.4.1.19 | S | synthase | |
CNHFAHCC_01156 | 1.7e-108 | yitE | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
CNHFAHCC_01157 | 5.4e-222 | yitF | 5.5.1.27 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
CNHFAHCC_01158 | 4e-229 | yitG | EGP | Major facilitator Superfamily | ||
CNHFAHCC_01159 | 1.8e-161 | yitH | K | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_01160 | 2e-82 | yjcF | S | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_01161 | 0.0 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | Catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
CNHFAHCC_01162 | 8.6e-55 | yajQ | S | Belongs to the UPF0234 family | ||
CNHFAHCC_01163 | 4e-161 | cvfB | S | protein conserved in bacteria | ||
CNHFAHCC_01164 | 8.5e-94 | |||||
CNHFAHCC_01165 | 2.2e-125 | |||||
CNHFAHCC_01166 | 1.5e-97 | S | Sporulation delaying protein SdpA | |||
CNHFAHCC_01167 | 1.5e-58 | K | Transcriptional regulator PadR-like family | |||
CNHFAHCC_01168 | 2e-95 | |||||
CNHFAHCC_01169 | 1.4e-44 | yitR | S | Domain of unknown function (DUF3784) | ||
CNHFAHCC_01170 | 2.2e-311 | nprB | 3.4.24.28 | E | Peptidase M4 | |
CNHFAHCC_01171 | 8.4e-159 | yitS | S | protein conserved in bacteria | ||
CNHFAHCC_01172 | 2.5e-147 | yitT | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
CNHFAHCC_01173 | 1.9e-72 | ipi | S | Intracellular proteinase inhibitor | ||
CNHFAHCC_01174 | 1.5e-26 | S | Protein of unknown function (DUF3813) | |||
CNHFAHCC_01175 | 1.9e-155 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
CNHFAHCC_01176 | 4.5e-143 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
CNHFAHCC_01177 | 4.7e-51 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
CNHFAHCC_01178 | 1.5e-22 | pilT | S | Proteolipid membrane potential modulator | ||
CNHFAHCC_01179 | 4.3e-272 | yitY | C | D-arabinono-1,4-lactone oxidase | ||
CNHFAHCC_01180 | 1.7e-88 | norB | G | Major Facilitator Superfamily | ||
CNHFAHCC_01181 | 5.4e-200 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
CNHFAHCC_01182 | 3.1e-231 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
CNHFAHCC_01183 | 2.2e-137 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
CNHFAHCC_01184 | 4.4e-219 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
CNHFAHCC_01185 | 3.9e-206 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
CNHFAHCC_01186 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase ammonia chain | |
CNHFAHCC_01187 | 3.8e-176 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
CNHFAHCC_01188 | 9.5e-28 | yjzC | S | YjzC-like protein | ||
CNHFAHCC_01189 | 2.3e-16 | yjzD | S | Protein of unknown function (DUF2929) | ||
CNHFAHCC_01190 | 6.2e-142 | yjaU | I | carboxylic ester hydrolase activity | ||
CNHFAHCC_01191 | 7.3e-103 | yjaV | ||||
CNHFAHCC_01192 | 8.5e-167 | med | S | Transcriptional activator protein med | ||
CNHFAHCC_01193 | 7.3e-26 | comZ | S | ComZ | ||
CNHFAHCC_01194 | 1.9e-23 | yjzB | ||||
CNHFAHCC_01195 | 3.9e-173 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
CNHFAHCC_01196 | 1.8e-234 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
CNHFAHCC_01197 | 7.8e-151 | yjaZ | O | Zn-dependent protease | ||
CNHFAHCC_01198 | 1.8e-184 | appD | P | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_01199 | 6.5e-187 | appF | E | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_01200 | 3.5e-48 | appA | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
CNHFAHCC_01201 | 1.9e-190 | appA | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
CNHFAHCC_01202 | 1.3e-171 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CNHFAHCC_01203 | 7.9e-163 | appC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CNHFAHCC_01204 | 5e-147 | yjbA | S | Belongs to the UPF0736 family | ||
CNHFAHCC_01205 | 6.1e-185 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
CNHFAHCC_01206 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
CNHFAHCC_01207 | 2.7e-166 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CNHFAHCC_01208 | 7.7e-166 | oppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CNHFAHCC_01209 | 3e-198 | oppD | P | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_01210 | 5.5e-172 | oppF | E | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_01211 | 3e-207 | yjbB | EGP | Major Facilitator Superfamily | ||
CNHFAHCC_01212 | 6.9e-104 | yjbC | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
CNHFAHCC_01213 | 2.1e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
CNHFAHCC_01214 | 6e-112 | yjbE | P | Integral membrane protein TerC family | ||
CNHFAHCC_01215 | 2.3e-116 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. Acts negatively in the development of competence by binding ComK and recruiting it to the ClpCP protease. When overexpressed, inhibits sporulation. Also involved in Spx degradation by ClpC | ||
CNHFAHCC_01216 | 2.3e-223 | yjbF | S | Competence protein | ||
CNHFAHCC_01217 | 0.0 | pepF | E | oligoendopeptidase F | ||
CNHFAHCC_01218 | 1.8e-20 | |||||
CNHFAHCC_01219 | 3.3e-169 | yjbH | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
CNHFAHCC_01220 | 3.7e-72 | yjbI | S | Bacterial-like globin | ||
CNHFAHCC_01221 | 1.5e-87 | yjbJ | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
CNHFAHCC_01222 | 2.4e-101 | yjbK | S | protein conserved in bacteria | ||
CNHFAHCC_01223 | 7.1e-62 | yjbL | S | Belongs to the UPF0738 family | ||
CNHFAHCC_01224 | 2.6e-112 | yjbM | 2.7.6.5 | S | GTP pyrophosphokinase | |
CNHFAHCC_01225 | 2.1e-151 | nadK | 2.7.1.23 | G | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
CNHFAHCC_01226 | 9.5e-161 | yjbO | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
CNHFAHCC_01227 | 3e-128 | prpE | 3.1.3.16, 3.6.1.41 | T | Asymmetrically hydrolyzes Ap4p to yield AMP and ATP | |
CNHFAHCC_01228 | 0.0 | yjbQ | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
CNHFAHCC_01229 | 3.4e-137 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
CNHFAHCC_01230 | 3.8e-108 | tenI | 2.5.1.3, 5.3.99.10 | H | Transcriptional regulator TenI | |
CNHFAHCC_01231 | 7.2e-219 | thiO | 1.4.3.19 | E | Glycine oxidase | |
CNHFAHCC_01232 | 3e-30 | thiS | H | thiamine diphosphate biosynthetic process | ||
CNHFAHCC_01233 | 1.5e-135 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
CNHFAHCC_01234 | 6e-188 | thiF | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
CNHFAHCC_01235 | 5.3e-150 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
CNHFAHCC_01236 | 3.2e-141 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
CNHFAHCC_01237 | 5.9e-54 | yjbX | S | Spore coat protein | ||
CNHFAHCC_01238 | 5.2e-83 | cotZ | S | Spore coat protein | ||
CNHFAHCC_01239 | 3.4e-96 | cotY | S | Spore coat protein Z | ||
CNHFAHCC_01240 | 6.4e-77 | cotX | S | Spore Coat Protein X and V domain | ||
CNHFAHCC_01241 | 3e-32 | cotW | ||||
CNHFAHCC_01242 | 2.3e-55 | cotV | S | Spore Coat Protein X and V domain | ||
CNHFAHCC_01243 | 8.7e-57 | yjcA | S | Protein of unknown function (DUF1360) | ||
CNHFAHCC_01246 | 2.9e-38 | spoVIF | S | Stage VI sporulation protein F | ||
CNHFAHCC_01247 | 0.0 | yjcD | 3.6.4.12 | L | DNA helicase | |
CNHFAHCC_01248 | 1.7e-38 | |||||
CNHFAHCC_01249 | 3e-72 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
CNHFAHCC_01250 | 2.9e-93 | yjcG | J | Belongs to the 2H phosphoesterase superfamily. YjcG family | ||
CNHFAHCC_01251 | 1.8e-138 | yjcH | P | COG2382 Enterochelin esterase and related enzymes | ||
CNHFAHCC_01252 | 3.8e-215 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
CNHFAHCC_01253 | 2.9e-218 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
CNHFAHCC_01254 | 3.7e-99 | rimJ | 2.3.1.128 | J | Alanine acetyltransferase | |
CNHFAHCC_01255 | 1.1e-212 | yjcL | S | Protein of unknown function (DUF819) | ||
CNHFAHCC_01258 | 2.1e-190 | S | Putative amidase domain | |||
CNHFAHCC_01259 | 2.6e-44 | yjcN | ||||
CNHFAHCC_01262 | 8.5e-81 | L | Transposase | |||
CNHFAHCC_01263 | 1.6e-72 | yjcP | ||||
CNHFAHCC_01264 | 4.1e-49 | S | YjcQ protein | |||
CNHFAHCC_01265 | 1.1e-92 | yqaS | L | DNA packaging | ||
CNHFAHCC_01266 | 2.2e-47 | yjcS | S | Antibiotic biosynthesis monooxygenase | ||
CNHFAHCC_01267 | 2.4e-141 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_01269 | 0.0 | manR | 2.7.1.200, 2.7.1.202 | GKT | transcriptional antiterminator | |
CNHFAHCC_01270 | 0.0 | manP | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
CNHFAHCC_01271 | 6.7e-189 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
CNHFAHCC_01272 | 4.8e-51 | yjdF | S | Protein of unknown function (DUF2992) | ||
CNHFAHCC_01273 | 2.5e-94 | yjdG | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
CNHFAHCC_01275 | 8e-82 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
CNHFAHCC_01276 | 4.2e-29 | S | Domain of unknown function (DUF4177) | |||
CNHFAHCC_01277 | 2.7e-52 | yjdJ | S | Domain of unknown function (DUF4306) | ||
CNHFAHCC_01278 | 3.3e-175 | cyoE | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
CNHFAHCC_01280 | 4.9e-265 | xynD | 3.5.1.104 | G | Polysaccharide deacetylase | |
CNHFAHCC_01281 | 5.5e-83 | S | Protein of unknown function (DUF2690) | |||
CNHFAHCC_01282 | 3.6e-21 | yjfB | S | Putative motility protein | ||
CNHFAHCC_01283 | 1.6e-171 | yjfC | O | Predicted Zn-dependent protease (DUF2268) | ||
CNHFAHCC_01284 | 2.2e-69 | T | PhoQ Sensor | |||
CNHFAHCC_01285 | 8.9e-104 | yjgB | S | Domain of unknown function (DUF4309) | ||
CNHFAHCC_01286 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase (NAD+) activity | |
CNHFAHCC_01287 | 4.3e-95 | yjgD | S | Protein of unknown function (DUF1641) | ||
CNHFAHCC_01288 | 8.7e-07 | S | Domain of unknown function (DUF4352) | |||
CNHFAHCC_01289 | 2e-117 | yjhB | 3.6.1.13, 3.6.1.55 | F | ADP-ribose pyrophosphatase | |
CNHFAHCC_01291 | 3.8e-226 | yjiB | 1.14.13.154, 1.14.15.8 | C | Cytochrome P450 | |
CNHFAHCC_01292 | 4.5e-219 | oleD | GT1 | CG | COG1819 Glycosyl transferases, related to UDP-glucuronosyltransferase | |
CNHFAHCC_01293 | 8.2e-30 | |||||
CNHFAHCC_01294 | 1.2e-146 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
CNHFAHCC_01295 | 1.9e-122 | ybbM | S | transport system, permease component | ||
CNHFAHCC_01296 | 5.2e-136 | pstB | 3.6.3.27 | P | ATPases associated with a variety of cellular activities | |
CNHFAHCC_01297 | 1.8e-176 | yjlA | EG | Putative multidrug resistance efflux transporter | ||
CNHFAHCC_01298 | 2.8e-93 | yjlB | S | Cupin domain | ||
CNHFAHCC_01299 | 7.1e-66 | yjlC | S | Protein of unknown function (DUF1641) | ||
CNHFAHCC_01300 | 2.6e-219 | yjlD | 1.6.99.3 | C | NADH dehydrogenase | |
CNHFAHCC_01301 | 1.1e-286 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
CNHFAHCC_01302 | 5.8e-250 | yjmB | G | symporter YjmB | ||
CNHFAHCC_01303 | 3e-195 | yjmC | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
CNHFAHCC_01304 | 1.6e-193 | rspB | 1.1.1.380 | E | Alcohol dehydrogenase GroES-like domain | |
CNHFAHCC_01305 | 4.7e-215 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
CNHFAHCC_01306 | 2.3e-153 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_01307 | 3.7e-227 | exuT | G | Sugar (and other) transporter | ||
CNHFAHCC_01308 | 2.3e-184 | exuR | K | transcriptional | ||
CNHFAHCC_01309 | 2.1e-287 | uxaB | 1.1.1.17, 1.1.1.58 | G | tagaturonate reductase activity | |
CNHFAHCC_01310 | 2e-288 | uxaA | 4.2.1.7, 4.4.1.24 | G | Altronate | |
CNHFAHCC_01311 | 4.3e-130 | MA20_18170 | S | membrane transporter protein | ||
CNHFAHCC_01312 | 3.3e-80 | yjoA | S | DinB family | ||
CNHFAHCC_01313 | 9.4e-247 | ftsH2 | 3.4.21.53 | O | AAA domain (dynein-related subfamily) | |
CNHFAHCC_01314 | 3e-212 | S | response regulator aspartate phosphatase | |||
CNHFAHCC_01316 | 6.3e-41 | S | YCII-related domain | |||
CNHFAHCC_01317 | 9.1e-170 | xlyA | 3.5.1.28 | CBM50 | M | N-acetylmuramoyl-L-alanine amidase |
CNHFAHCC_01318 | 2.1e-61 | yjqA | S | Bacterial PH domain | ||
CNHFAHCC_01319 | 4.2e-112 | yjqB | S | Pfam:DUF867 | ||
CNHFAHCC_01320 | 4.4e-160 | ydbD | P | Catalase | ||
CNHFAHCC_01321 | 1.6e-111 | xkdA | E | IrrE N-terminal-like domain | ||
CNHFAHCC_01322 | 3.2e-56 | xre | K | Helix-turn-helix XRE-family like proteins | ||
CNHFAHCC_01324 | 5.9e-157 | xkdB | K | sequence-specific DNA binding | ||
CNHFAHCC_01325 | 6.4e-119 | xkdC | L | Bacterial dnaA protein | ||
CNHFAHCC_01329 | 4.6e-10 | yqaO | S | Phage-like element PBSX protein XtrA | ||
CNHFAHCC_01330 | 4.4e-86 | xpf | K | COG1595 DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog | ||
CNHFAHCC_01331 | 4.8e-140 | xtmA | L | phage terminase small subunit | ||
CNHFAHCC_01332 | 9.6e-255 | xtmB | S | phage terminase, large subunit | ||
CNHFAHCC_01333 | 5.4e-286 | yqbA | S | portal protein | ||
CNHFAHCC_01334 | 1.2e-133 | yqbD | 2.1.1.72 | L | Putative phage serine protease XkdF | |
CNHFAHCC_01335 | 5.8e-169 | xkdG | S | Phage capsid family | ||
CNHFAHCC_01336 | 5.5e-65 | yqbG | S | Protein of unknown function (DUF3199) | ||
CNHFAHCC_01337 | 8.7e-65 | yqbH | S | Domain of unknown function (DUF3599) | ||
CNHFAHCC_01338 | 4.4e-88 | xkdI | S | Bacteriophage HK97-gp10, putative tail-component | ||
CNHFAHCC_01339 | 1.9e-77 | xkdJ | ||||
CNHFAHCC_01340 | 3.8e-31 | |||||
CNHFAHCC_01341 | 2.5e-256 | xkdK | S | Phage tail sheath C-terminal domain | ||
CNHFAHCC_01342 | 6.1e-76 | xkdM | S | Phage tail tube protein | ||
CNHFAHCC_01343 | 1.9e-77 | S | Phage XkdN-like tail assembly chaperone protein, TAC | |||
CNHFAHCC_01344 | 0.0 | xkdO | L | Transglycosylase SLT domain | ||
CNHFAHCC_01345 | 6.9e-122 | xkdP | S | Lysin motif | ||
CNHFAHCC_01346 | 4.8e-182 | yqbQ | 3.2.1.96 | G | NLP P60 protein | |
CNHFAHCC_01347 | 2.1e-39 | xkdR | S | Protein of unknown function (DUF2577) | ||
CNHFAHCC_01348 | 9.6e-71 | xkdS | S | Protein of unknown function (DUF2634) | ||
CNHFAHCC_01349 | 1.2e-191 | xkdT | S | Evidence 3 Function proposed based on presence of conserved amino acid motif, structural feature or limited homology | ||
CNHFAHCC_01350 | 9e-101 | xkdU | S | Uncharacterised protein conserved in bacteria (DUF2313) | ||
CNHFAHCC_01351 | 6.7e-41 | |||||
CNHFAHCC_01352 | 0.0 | |||||
CNHFAHCC_01353 | 2.6e-55 | xkdW | S | XkdW protein | ||
CNHFAHCC_01354 | 1.7e-23 | xkdX | ||||
CNHFAHCC_01355 | 1.2e-154 | xepA | ||||
CNHFAHCC_01356 | 2.8e-39 | xhlA | S | Haemolysin XhlA | ||
CNHFAHCC_01357 | 9.3e-40 | xhlB | S | SPP1 phage holin | ||
CNHFAHCC_01358 | 1.2e-163 | xlyA | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
CNHFAHCC_01359 | 6.7e-23 | spoIISB | S | Stage II sporulation protein SB | ||
CNHFAHCC_01360 | 1.8e-136 | spoIISA | S | Toxin SpoIISA, type II toxin-antitoxin system | ||
CNHFAHCC_01361 | 5.8e-175 | pit | P | phosphate transporter | ||
CNHFAHCC_01362 | 6.9e-110 | ykaA | P | COG1392 Phosphate transport regulator (distant homolog of PhoU) | ||
CNHFAHCC_01363 | 9.4e-242 | steT | E | amino acid | ||
CNHFAHCC_01364 | 7.2e-183 | mhqA | E | COG0346 Lactoylglutathione lyase and related lyases | ||
CNHFAHCC_01366 | 0.0 | ykcB | M | COG1807 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
CNHFAHCC_01367 | 1.3e-179 | ykcC | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
CNHFAHCC_01369 | 8.5e-214 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
CNHFAHCC_01370 | 1e-137 | proG | 1.5.1.2 | E | Pyrroline-5-carboxylate reductase | |
CNHFAHCC_01371 | 7.9e-154 | dppA | E | D-aminopeptidase | ||
CNHFAHCC_01372 | 4.5e-155 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CNHFAHCC_01373 | 3.9e-176 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
CNHFAHCC_01374 | 3.4e-191 | dppD | P | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_01375 | 0.0 | dppE | E | ABC transporter substrate-binding protein | ||
CNHFAHCC_01377 | 8.1e-179 | ykfA | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
CNHFAHCC_01378 | 3.2e-203 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
CNHFAHCC_01379 | 5.3e-172 | ykfC | 3.4.14.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
CNHFAHCC_01380 | 7.7e-188 | ykfD | E | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_01381 | 7.4e-205 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
CNHFAHCC_01382 | 5.3e-161 | ykgA | E | Amidinotransferase | ||
CNHFAHCC_01383 | 1.5e-92 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
CNHFAHCC_01384 | 1e-226 | hmp | 1.14.12.17 | C | Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress | |
CNHFAHCC_01385 | 1e-07 | |||||
CNHFAHCC_01386 | 5.4e-130 | ykjA | S | Protein of unknown function (DUF421) | ||
CNHFAHCC_01387 | 1e-98 | ykkA | S | Protein of unknown function (DUF664) | ||
CNHFAHCC_01388 | 1e-98 | ykkB | 2.3.1.128 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
CNHFAHCC_01389 | 3.5e-55 | ykkC | P | Multidrug resistance protein | ||
CNHFAHCC_01390 | 1.1e-50 | ykkD | P | Multidrug resistance protein | ||
CNHFAHCC_01391 | 3.9e-170 | purU | 2.7.7.72, 3.5.1.10 | F | Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4) | |
CNHFAHCC_01392 | 1.3e-31 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
CNHFAHCC_01393 | 4.9e-19 | rom | S | Rop protein | ||
CNHFAHCC_01394 | 2.9e-63 | mbeC | S | Psort location Cytoplasmic, score | ||
CNHFAHCC_01395 | 1.2e-214 | tetA | EGP | Sugar (and other) transporter | ||
CNHFAHCC_01396 | 1.2e-242 | tetL | EGP | Major Facilitator Superfamily | ||
CNHFAHCC_01397 | 2e-160 | penP | 3.5.2.6 | V | Beta-lactamase | |
CNHFAHCC_01398 | 3.9e-205 | macB | V | MacB-like periplasmic core domain | ||
CNHFAHCC_01399 | 3.4e-83 | fur | K | Ferric uptake regulator family | ||
CNHFAHCC_01400 | 1.4e-158 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
CNHFAHCC_01401 | 3.2e-289 | purH | 2.1.2.3, 3.5.4.10 | F | AICARFT/IMPCHase bienzyme | |
CNHFAHCC_01402 | 3.7e-64 | |||||
CNHFAHCC_01403 | 3.6e-179 | ubiE | Q | Methyltransferase small domain | ||
CNHFAHCC_01404 | 2.5e-52 | S | Domain of unknown function (DUF3067) | |||
CNHFAHCC_01405 | 2.9e-208 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_01406 | 3.5e-193 | trxB2 | 1.8.1.9 | O | Pyridine nucleotide-disulphide oxidoreductase | |
CNHFAHCC_01407 | 3.5e-35 | S | GLTT repeat (6 copies) | |||
CNHFAHCC_01408 | 6e-43 | |||||
CNHFAHCC_01409 | 4.7e-114 | |||||
CNHFAHCC_01410 | 0.0 | dnaE | 2.7.7.7 | F | DNA polymerase alpha chain like domain | |
CNHFAHCC_01412 | 0.0 | lepA | J | GTP-binding protein LepA C-terminus | ||
CNHFAHCC_01413 | 1.1e-196 | yqjG | 1.8.5.7, 2.5.1.18 | O | Glutathione S-transferase, C-terminal domain | |
CNHFAHCC_01414 | 4.2e-183 | waaQ | GT9 | M | Glycosyltransferase family 9 (heptosyltransferase) | |
CNHFAHCC_01415 | 5.5e-65 | T | Cyclic nucleotide-monophosphate binding domain | |||
CNHFAHCC_01416 | 1.6e-131 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | F | Phosphoribosyl-AMP cyclohydrolase | |
CNHFAHCC_01417 | 5.4e-185 | S | metal chaperone, involved in Zn homeostasis, GTPase of COG0523 family | |||
CNHFAHCC_01418 | 8.2e-140 | S | ABC-2 family transporter protein | |||
CNHFAHCC_01420 | 1.5e-175 | sds | 2.5.1.84, 2.5.1.85 | H | Polyprenyl synthetase | |
CNHFAHCC_01421 | 1.6e-110 | rluE | 5.4.99.20, 5.4.99.22 | J | RNA pseudouridylate synthase | |
CNHFAHCC_01422 | 8.4e-93 | |||||
CNHFAHCC_01423 | 3.7e-136 | KLT | ARM-like repeat domain, GUN4-N terminal | |||
CNHFAHCC_01424 | 5.8e-213 | acsF | 1.14.13.81, 1.16.3.1, 4.1.99.5 | F | Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) | |
CNHFAHCC_01425 | 1.4e-183 | fcl | 1.1.1.271 | GM | Catalyzes the two-step NADP-dependent conversion of GDP- 4-dehydro-6-deoxy-D-mannose to GDP-fucose, involving an epimerase and a reductase reaction | |
CNHFAHCC_01426 | 1.7e-212 | gmd | 4.2.1.47 | M | Catalyzes the conversion of GDP-D-mannose to GDP-4- dehydro-6-deoxy-D-mannose | |
CNHFAHCC_01427 | 4.6e-210 | pufM | 1.10.3.9 | C | Photosystem II (PSII) is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1 D2 (PsbA PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors | |
CNHFAHCC_01429 | 0.0 | speA | 4.1.1.19 | E | Catalyzes the biosynthesis of agmatine from arginine | |
CNHFAHCC_01430 | 0.0 | ligA | 2.7.7.7, 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
CNHFAHCC_01431 | 5.7e-106 | S | Putative restriction endonuclease | |||
CNHFAHCC_01432 | 3.7e-177 | yfiZ | U | FecCD transport family | ||
CNHFAHCC_01433 | 1.9e-189 | fecD | U | FecCD transport family | ||
CNHFAHCC_01434 | 8.9e-150 | yusV | 3.6.3.34 | HP | ATPases associated with a variety of cellular activities | |
CNHFAHCC_01435 | 1.6e-179 | yfiY | P | Periplasmic binding protein | ||
CNHFAHCC_01436 | 0.0 | iutA | P | TonB dependent receptor | ||
CNHFAHCC_01437 | 4.8e-190 | K | helix_turn_helix, arabinose operon control protein | |||
CNHFAHCC_01438 | 2.1e-222 | mefE | EGP | Major facilitator superfamily | ||
CNHFAHCC_01439 | 7e-194 | O | PFAM Sucrase ferredoxin-like | |||
CNHFAHCC_01440 | 3.4e-183 | P | ABC-type Fe3 -hydroxamate transport system, periplasmic component | |||
CNHFAHCC_01441 | 0.0 | P | TonB dependent receptor | |||
CNHFAHCC_01442 | 2.3e-198 | K | COGs COG2207 AraC-type DNA-binding domain-containing protein | |||
CNHFAHCC_01443 | 1.9e-152 | 2.1.1.163, 2.1.1.201 | Q | Methyltransferase type 11 | ||
CNHFAHCC_01444 | 0.0 | P | TonB dependent receptor | |||
CNHFAHCC_01445 | 2e-65 | exbD | U | Biopolymer transport protein ExbD/TolR | ||
CNHFAHCC_01446 | 5.8e-104 | U | MotA/TolQ/ExbB proton channel family | |||
CNHFAHCC_01447 | 3.4e-177 | M | Gram-negative bacterial TonB protein C-terminal | |||
CNHFAHCC_01448 | 2.8e-18 | XK27_09805 | 2.7.11.1 | S | Possible plasma membrane-binding motif in junctophilins, PIP-5-kinases and protein kinases. | |
CNHFAHCC_01449 | 0.0 | V | ABC transporter transmembrane region | |||
CNHFAHCC_01450 | 4e-192 | K | COGs COG2207 AraC-type DNA-binding domain-containing protein | |||
CNHFAHCC_01451 | 3.5e-200 | P | COGs COG4773 Outer membrane receptor for ferric coprogen and ferric-rhodotorulic acid | |||
CNHFAHCC_01452 | 2.8e-246 | P | COGs COG4773 Outer membrane receptor for ferric coprogen and ferric-rhodotorulic acid | |||
CNHFAHCC_01453 | 1.1e-186 | fecB | P | COGs COG0614 ABC-type Fe3 -hydroxamate transport system periplasmic component | ||
CNHFAHCC_01454 | 1.5e-175 | fecB | P | Periplasmic binding protein | ||
CNHFAHCC_01455 | 3.6e-69 | S | Protein of unknown function (DUF1636) | |||
CNHFAHCC_01456 | 0.0 | V | ABC transporter transmembrane region | |||
CNHFAHCC_01457 | 3.7e-176 | |||||
CNHFAHCC_01458 | 2.1e-60 | |||||
CNHFAHCC_01459 | 5.5e-36 | S | Protein of unknown function (DUF433) | |||
CNHFAHCC_01460 | 4.7e-240 | S | Domain of unknown function (DUF4336) | |||
CNHFAHCC_01461 | 2.8e-57 | psb28 | S | Psb28 protein | ||
CNHFAHCC_01462 | 0.0 | dinG | 3.6.4.12 | KL | COG1199 Rad3-related DNA | |
CNHFAHCC_01463 | 6e-17 | L | Transposase DDE domain | |||
CNHFAHCC_01464 | 4.6e-157 | L | Transposase | |||
CNHFAHCC_01465 | 1.9e-121 | |||||
CNHFAHCC_01466 | 4.2e-222 | hypD | O | Hydrogenase formation hypA family | ||
CNHFAHCC_01467 | 1.3e-154 | rfbD | 1.1.1.133 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
CNHFAHCC_01468 | 1.1e-129 | msrA | 1.8.4.11 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
CNHFAHCC_01469 | 3e-305 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
CNHFAHCC_01470 | 1.5e-106 | K | Bacterial regulatory proteins, tetR family | |||
CNHFAHCC_01471 | 5.3e-132 | K | PFAM Acetyltransferase (GNAT) family | |||
CNHFAHCC_01472 | 9.4e-186 | V | ATPases associated with a variety of cellular activities | |||
CNHFAHCC_01473 | 0.0 | CP | transmembrane transport | |||
CNHFAHCC_01474 | 3e-136 | Q | AdoMet dependent proline di-methyltransferase | |||
CNHFAHCC_01475 | 2.2e-101 | S | DinB family | |||
CNHFAHCC_01476 | 6.9e-144 | Q | methyltransferase | |||
CNHFAHCC_01477 | 0.0 | 3.1.4.46 | S | Calcineurin-like phosphoesterase | ||
CNHFAHCC_01478 | 8.3e-142 | 2.4.1.187 | GT26 | M | Glycosyl transferase WecB/TagA/CpsF family | |
CNHFAHCC_01479 | 1.9e-126 | yeaZ | O | Glycoprotease family | ||
CNHFAHCC_01480 | 4e-138 | tesA | E | GDSL-like Lipase/Acylhydrolase family | ||
CNHFAHCC_01481 | 2.5e-54 | |||||
CNHFAHCC_01482 | 9.9e-62 | zmpC | D | nuclear chromosome segregation | ||
CNHFAHCC_01483 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
CNHFAHCC_01484 | 8.9e-40 | |||||
CNHFAHCC_01485 | 2.8e-45 | S | Peptidase propeptide and YPEB domain | |||
CNHFAHCC_01486 | 1.8e-158 | pilD | 3.4.23.43 | NOU | Cleaves type-4 fimbrial leader sequence and methylates the N-terminal (generally Phe) residue | |
CNHFAHCC_01487 | 1.7e-96 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
CNHFAHCC_01488 | 9.7e-152 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
CNHFAHCC_01489 | 5.5e-61 | trxM2 | 5.3.4.1 | O | Thioredoxin | |
CNHFAHCC_01490 | 1.4e-27 | S | Protein of unknown function (DUF2442) | |||
CNHFAHCC_01491 | 4.4e-28 | S | Domain of unknown function (DUF4160) | |||
CNHFAHCC_01492 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
CNHFAHCC_01493 | 4.1e-141 | S | Alternative locus ID | |||
CNHFAHCC_01494 | 7.9e-105 | nudF | 3.6.1.13 | L | NUDIX domain | |
CNHFAHCC_01495 | 2.5e-233 | M | Barrel-sandwich domain of CusB or HlyD membrane-fusion | |||
CNHFAHCC_01496 | 3.8e-102 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
CNHFAHCC_01497 | 5.2e-248 | gpmB | 3.1.3.3, 3.1.3.73 | G | Histidine phosphatase superfamily (branch 1) | |
CNHFAHCC_01498 | 3.2e-239 | crtX | 2.4.1.276 | GT1 | CG | UDP-glucoronosyl and UDP-glucosyl transferase |
CNHFAHCC_01499 | 3e-60 | S | Sulfite exporter TauE/SafE | |||
CNHFAHCC_01500 | 6.3e-114 | cpcF | 4.4.1.32 | C | PBS lyase HEAT-like repeat | |
CNHFAHCC_01501 | 0.0 | E | Transglutaminase/protease-like homologues | |||
CNHFAHCC_01502 | 2.2e-145 | O | Heat shock protein | |||
CNHFAHCC_01503 | 1.2e-137 | hflC | O | prohibitin homologues | ||
CNHFAHCC_01504 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
CNHFAHCC_01505 | 2.7e-101 | rnhB | 3.1.26.4 | J | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CNHFAHCC_01506 | 2e-73 | mutY | 3.6.1.55 | L | NUDIX domain | |
CNHFAHCC_01507 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
CNHFAHCC_01508 | 2.3e-98 | lepB | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
CNHFAHCC_01509 | 7.4e-253 | me | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
CNHFAHCC_01510 | 1.8e-189 | cysB | 2.5.1.47 | E | Pyridoxal-phosphate dependent enzyme | |
CNHFAHCC_01511 | 5.5e-183 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
CNHFAHCC_01512 | 0.0 | |||||
CNHFAHCC_01513 | 2.4e-272 | V | restriction endodeoxyribonuclease activity | |||
CNHFAHCC_01514 | 1.8e-156 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
CNHFAHCC_01515 | 1.2e-129 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
CNHFAHCC_01516 | 1.6e-207 | S | chaperone-mediated protein folding | |||
CNHFAHCC_01517 | 1.5e-55 | sohA | K | prlF antitoxin for toxin YhaV_toxin | ||
CNHFAHCC_01518 | 4.4e-75 | yhaV | S | Toxin with endonuclease activity, of toxin-antitoxin system | ||
CNHFAHCC_01520 | 9.6e-226 | rfaL | M | O-Antigen ligase | ||
CNHFAHCC_01521 | 4.1e-47 | S | Protein of unknown function (DUF3181) | |||
CNHFAHCC_01522 | 1.9e-68 | S | Protein of unknown function (DUF3119) | |||
CNHFAHCC_01523 | 3.3e-201 | DZ | Protein of unknown function (DUF3086) | |||
CNHFAHCC_01524 | 4.2e-225 | nifS | 2.8.1.7 | E | Aminotransferase class-V | |
CNHFAHCC_01525 | 5.1e-73 | S | Phosphate-starvation-inducible E | |||
CNHFAHCC_01526 | 2e-238 | 1.3.5.5, 1.6.1.1, 1.8.1.4 | C | Pyridine nucleotide-disulphide oxidoreductase | ||
CNHFAHCC_01527 | 2.3e-63 | P | alginic acid biosynthetic process | |||
CNHFAHCC_01528 | 4.4e-20 | |||||
CNHFAHCC_01529 | 4.9e-176 | xerC | L | Phage integrase, N-terminal SAM-like domain | ||
CNHFAHCC_01530 | 1.1e-41 | |||||
CNHFAHCC_01531 | 5.1e-220 | forZ | 1.4.3.19, 1.4.3.3 | E | FAD dependent oxidoreductase | |
CNHFAHCC_01532 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_01533 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_01534 | 0.0 | nblS | 2.7.13.3 | T | HAMP domain | |
CNHFAHCC_01535 | 5.8e-76 | psaD | S | PsaD | ||
CNHFAHCC_01536 | 1e-300 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
CNHFAHCC_01537 | 5.8e-164 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Polyprenyl synthetase | |
CNHFAHCC_01538 | 2.2e-69 | |||||
CNHFAHCC_01539 | 4.4e-155 | S | CAAX protease self-immunity | |||
CNHFAHCC_01540 | 1.6e-120 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
CNHFAHCC_01541 | 1.8e-78 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
CNHFAHCC_01542 | 1.6e-212 | nusA | K | Participates in both transcription termination and antitermination | ||
CNHFAHCC_01543 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
CNHFAHCC_01544 | 1.1e-124 | 2.5.1.18 | O | Glutathione S-transferase, N-terminal domain | ||
CNHFAHCC_01545 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Carbohydrate-binding module 48 (Isoamylase N-terminal domain) |
CNHFAHCC_01546 | 9.6e-71 | KLT | serine threonine protein kinase | |||
CNHFAHCC_01547 | 3.6e-48 | L | DDE superfamily endonuclease | |||
CNHFAHCC_01548 | 2.2e-145 | cobM | 1.3.1.76, 2.1.1.131, 2.1.1.133, 2.1.1.271, 3.7.1.12, 4.99.1.4 | H | Tetrapyrrole (Corrin/Porphyrin) Methylases | |
CNHFAHCC_01549 | 1.1e-71 | K | Penicillinase repressor | |||
CNHFAHCC_01550 | 1.2e-162 | O | Peptidase family M48 | |||
CNHFAHCC_01551 | 7.3e-91 | bcp | 1.11.1.15 | O | Redoxin | |
CNHFAHCC_01552 | 1.7e-96 | |||||
CNHFAHCC_01553 | 4.7e-51 | yqgV | S | Thiamine-binding protein | ||
CNHFAHCC_01554 | 7.4e-155 | T | Universal stress protein family | |||
CNHFAHCC_01556 | 9.6e-185 | acuC | BQ | Histone deacetylase domain | ||
CNHFAHCC_01557 | 4.2e-180 | speB | 3.5.3.11 | E | Arginase family | |
CNHFAHCC_01558 | 2.7e-137 | ppiB | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
CNHFAHCC_01559 | 4.5e-100 | ycf4 | S | Seems to be required for the assembly of the photosystem I complex | ||
CNHFAHCC_01560 | 9.7e-307 | IQ | GH3 auxin-responsive promoter | |||
CNHFAHCC_01561 | 4.3e-169 | ET | Bacterial periplasmic substrate-binding proteins | |||
CNHFAHCC_01562 | 1.4e-68 | S | Domain of unknown function (DUF1818) | |||
CNHFAHCC_01563 | 5.6e-92 | lptA | S | OstA-like protein | ||
CNHFAHCC_01564 | 4.7e-137 | lptB | S | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_01565 | 9.2e-144 | cobK | 1.3.1.106, 1.3.1.54, 1.3.1.76, 2.1.1.131, 2.1.1.132, 3.7.1.12, 4.99.1.4 | H | Precorrin-6x reductase CbiJ/CobK | |
CNHFAHCC_01566 | 8.3e-33 | psaK | U | Photosystem I psaG / psaK | ||
CNHFAHCC_01567 | 6.1e-10 | S | Protein conserved in bacteria | |||
CNHFAHCC_01568 | 9.1e-276 | nuoN | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_01569 | 4.2e-194 | phoA | 3.1.3.1 | S | Calcineurin-like phosphoesterase | |
CNHFAHCC_01570 | 3.2e-144 | S | RDD family | |||
CNHFAHCC_01571 | 4.3e-103 | bcp | 1.11.1.15 | O | Redoxin | |
CNHFAHCC_01572 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
CNHFAHCC_01573 | 0.0 | norV | 1.6.3.4 | C | Mediates electron transfer from NADH to oxygen, reducing it to water. This modular protein has 3 redox cofactors, in other organisms the same activity requires 2 or 3 proteins (By similarity) | |
CNHFAHCC_01574 | 1.6e-83 | S | PFAM Phosphate-starvation-inducible E | |||
CNHFAHCC_01575 | 0.0 | norV | 1.6.3.4 | C | Mediates electron transfer from NADH to oxygen, reducing it to water. This modular protein has 3 redox cofactors, in other organisms the same activity requires 2 or 3 proteins | |
CNHFAHCC_01576 | 1.7e-257 | ctpB | 3.4.21.102 | M | tail specific protease | |
CNHFAHCC_01577 | 2.7e-117 | yciO | 2.7.7.87 | J | Telomere recombination | |
CNHFAHCC_01578 | 7.7e-249 | larC | 4.99.1.12 | S | Protein of unknown function DUF111 | |
CNHFAHCC_01579 | 3.7e-163 | atpG | F | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
CNHFAHCC_01580 | 5.1e-276 | atpA | 3.6.3.14 | F | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
CNHFAHCC_01581 | 3.4e-92 | atpH | F | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
CNHFAHCC_01582 | 3.3e-52 | atpF | C | ATP synthase F(0) sector subunit b | ||
CNHFAHCC_01583 | 8.6e-35 | atpF | C | ATP synthase F(0) sector subunit b' | ||
CNHFAHCC_01584 | 2.5e-31 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
CNHFAHCC_01585 | 4.1e-133 | atpI | C | it plays a direct role in the translocation of protons across the membrane | ||
CNHFAHCC_01586 | 1.1e-60 | atp1 | U | atp synthase | ||
CNHFAHCC_01587 | 5.9e-263 | era | S | Domain of unknown function (DUF697) | ||
CNHFAHCC_01588 | 2.3e-256 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_01589 | 2.4e-214 | S | Domain of unknown function (DUF4350) | |||
CNHFAHCC_01590 | 3.2e-175 | moxR2 | O | ATPase family associated with various cellular activities (AAA) | ||
CNHFAHCC_01591 | 1.4e-62 | ycf57 | S | Iron-sulphur cluster biosynthesis | ||
CNHFAHCC_01592 | 2.9e-179 | eamA1 | U | EamA-like transporter family | ||
CNHFAHCC_01593 | 1.8e-124 | S | HAS barrel domain | |||
CNHFAHCC_01594 | 1.5e-146 | mkl | Q | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_01595 | 0.0 | ybiO | M | Mechanosensitive ion channel | ||
CNHFAHCC_01596 | 4.5e-111 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
CNHFAHCC_01598 | 5.2e-155 | S | Protein of unknown function (DUF429) | |||
CNHFAHCC_01599 | 2.3e-192 | S | A predicted alpha-helical domain with a conserved ER motif. | |||
CNHFAHCC_01600 | 7.4e-123 | S | Putative restriction endonuclease | |||
CNHFAHCC_01601 | 1.4e-270 | lpdA | 1.16.1.1, 1.8.1.4 | F | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
CNHFAHCC_01602 | 6.9e-89 | S | Pfam:DUF1817 | |||
CNHFAHCC_01603 | 9e-104 | C | HEAT repeat | |||
CNHFAHCC_01604 | 3.7e-111 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
CNHFAHCC_01605 | 1e-71 | |||||
CNHFAHCC_01606 | 2.3e-76 | uspA | T | Universal stress protein family | ||
CNHFAHCC_01607 | 0.0 | T | Forkhead associated domain | |||
CNHFAHCC_01608 | 0.0 | T | Inner membrane component of T3SS, cytoplasmic domain | |||
CNHFAHCC_01609 | 0.0 | T | Forkhead associated domain | |||
CNHFAHCC_01610 | 0.0 | typA | T | Elongation factor G C-terminus | ||
CNHFAHCC_01611 | 9.2e-278 | S | NMT1-like family | |||
CNHFAHCC_01612 | 3.6e-173 | 3.1.26.11 | S | Beta-lactamase superfamily domain | ||
CNHFAHCC_01613 | 2.9e-29 | |||||
CNHFAHCC_01614 | 2.5e-118 | upp | 2.4.2.9 | F | Uracil phosphoribosyltransferase | |
CNHFAHCC_01615 | 7.4e-147 | hflC | O | prohibitin homologues | ||
CNHFAHCC_01616 | 3.6e-257 | |||||
CNHFAHCC_01617 | 0.0 | prpC | 3.1.3.16 | KLT | Serine/threonine phosphatases, family 2C, catalytic domain | |
CNHFAHCC_01618 | 1e-125 | yrdA | S | Carbon dioxide concentrating mechanism protein | ||
CNHFAHCC_01619 | 0.0 | ccmM | C | Ribulose bisphosphate carboxylase, small chain | ||
CNHFAHCC_01620 | 1.6e-48 | ccmL | CQ | Ethanolamine utilisation protein EutN/carboxysome | ||
CNHFAHCC_01621 | 6.1e-52 | ccmK1 | CQ | BMC | ||
CNHFAHCC_01622 | 1.4e-47 | CQ | BMC | |||
CNHFAHCC_01623 | 9.1e-302 | gltD | 1.4.1.13, 1.4.1.14 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
CNHFAHCC_01624 | 9.7e-178 | yplB | S | Ankyrin repeat | ||
CNHFAHCC_01625 | 1e-92 | S | Protein of unknown function (DUF1092) | |||
CNHFAHCC_01626 | 9.7e-219 | 3.5.1.24 | M | PFAM Linear amide C-N hydrolases, choloylglycine hydrolase family | ||
CNHFAHCC_01627 | 1.8e-294 | S | RNase_H superfamily | |||
CNHFAHCC_01628 | 5.2e-147 | S | Predicted periplasmic protein (DUF2092) | |||
CNHFAHCC_01629 | 1.8e-60 | |||||
CNHFAHCC_01630 | 0.0 | U | Sulfate permease family | |||
CNHFAHCC_01631 | 7e-212 | pcxA | U | Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport | ||
CNHFAHCC_01632 | 0.0 | bchD | 6.6.1.1 | H | magnesium ion into protoporphyrin IX to yield | |
CNHFAHCC_01633 | 2.9e-11 | |||||
CNHFAHCC_01634 | 1.7e-101 | |||||
CNHFAHCC_01635 | 1.4e-278 | speA | 4.1.1.18, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, major domain | |
CNHFAHCC_01636 | 2.8e-191 | ald | 1.4.1.1 | E | Alanine dehydrogenase/PNT, C-terminal domain | |
CNHFAHCC_01637 | 4.7e-118 | pdxJ | 2.6.99.2 | H | Catalyzes the complicated ring closure reaction between the two acyclic compounds 1-deoxy-D-xylulose-5-phosphate (DXP) and 3-amino-2-oxopropyl phosphate (1-amino-acetone-3-phosphate or AAP) to form pyridoxine 5'-phosphate (PNP) and inorganic phosphate | |
CNHFAHCC_01638 | 1.2e-52 | ycf54 | S | Protein of unknown function (DUF2488) | ||
CNHFAHCC_01639 | 7.1e-272 | D | Transglutaminase/protease-like homologues | |||
CNHFAHCC_01640 | 2.9e-101 | msrB | 1.8.4.12 | O | SelR domain | |
CNHFAHCC_01641 | 3.8e-218 | hhoA | 3.4.21.107 | O | Trypsin | |
CNHFAHCC_01642 | 5e-125 | ycf29 | T | helix_turn_helix, Lux Regulon | ||
CNHFAHCC_01643 | 6.9e-189 | bvdR | 1.3.1.24 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
CNHFAHCC_01644 | 1.7e-91 | spmB | S | PFAM Nucleoside recognition | ||
CNHFAHCC_01645 | 2.6e-104 | spmA | S | Nucleoside recognition | ||
CNHFAHCC_01646 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
CNHFAHCC_01647 | 1.8e-83 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
CNHFAHCC_01648 | 2.2e-207 | thiL | 2.7.4.16 | H | Catalyzes the ATP-dependent phosphorylation of thiamine- monophosphate (TMP) to form thiamine-pyrophosphate (TPP), the active form of vitamin B1 | |
CNHFAHCC_01649 | 7.2e-200 | |||||
CNHFAHCC_01650 | 2.4e-278 | |||||
CNHFAHCC_01651 | 1.2e-252 | T | COG3706 Response regulator containing a CheY-like receiver domain and a GGDEF domain | |||
CNHFAHCC_01652 | 0.0 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_01653 | 6.6e-85 | yafP | 5.3.1.16 | K | Acetyltransferase (GNAT) domain | |
CNHFAHCC_01654 | 1.8e-96 | S | Copper resistance protein D | |||
CNHFAHCC_01655 | 1.1e-141 | cysH | 1.8.4.10, 1.8.4.8 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
CNHFAHCC_01656 | 2.2e-210 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
CNHFAHCC_01658 | 9.2e-101 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
CNHFAHCC_01659 | 8.2e-205 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
CNHFAHCC_01660 | 7.2e-29 | S | Protein of unknown function (DUF2862) | |||
CNHFAHCC_01661 | 4.5e-205 | arsA | 3.6.3.16 | OP | Anion-transporting ATPase | |
CNHFAHCC_01662 | 4.2e-119 | msrA | 1.8.4.11 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
CNHFAHCC_01663 | 4.5e-48 | S | Protein of unknown function (DUF2288) | |||
CNHFAHCC_01664 | 2.1e-34 | S | Tetratricopeptide repeat | |||
CNHFAHCC_01665 | 6.5e-93 | O | DnaJ molecular chaperone homology domain | |||
CNHFAHCC_01666 | 1.4e-110 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
CNHFAHCC_01667 | 1.1e-264 | kefA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
CNHFAHCC_01669 | 5.2e-186 | wcaA | 2.4.1.175, 2.4.1.226 | GT2 | S | Glycosyltransferase like family 2 |
CNHFAHCC_01670 | 2.2e-69 | nblB | C | PBS lyase HEAT-like repeat | ||
CNHFAHCC_01671 | 2e-166 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
CNHFAHCC_01673 | 2.9e-299 | pleD | T | MASE1 | ||
CNHFAHCC_01674 | 2.8e-30 | S | ChrR Cupin-like domain | |||
CNHFAHCC_01675 | 2.5e-109 | spoT | 2.7.6.5, 3.1.7.2 | KT | HD domain | |
CNHFAHCC_01676 | 1.8e-228 | mqnC | 1.21.98.1, 2.5.1.120, 2.5.1.77, 4.1.99.19 | H | Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) | |
CNHFAHCC_01677 | 3.7e-87 | E | glyoxalase bleomycin resistance protein dioxygenase | |||
CNHFAHCC_01678 | 0.0 | S | Tetratricopeptide repeat | |||
CNHFAHCC_01679 | 2.3e-193 | |||||
CNHFAHCC_01680 | 5.1e-99 | C | Protein of unknown function (DUF3611) | |||
CNHFAHCC_01681 | 1.9e-160 | birA | 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
CNHFAHCC_01682 | 4.3e-68 | usp | T | Universal stress protein family | ||
CNHFAHCC_01683 | 7.6e-137 | ubiE | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of 2- phytyl-1,4-beta-naphthoquinol to phylloquinol | |
CNHFAHCC_01684 | 1.9e-58 | bsr | 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
CNHFAHCC_01686 | 1.3e-26 | S | CopG antitoxin of type II toxin-antitoxin system | |||
CNHFAHCC_01687 | 4.2e-280 | icd | 1.1.1.42 | C | Isocitrate/isopropylmalate dehydrogenase | |
CNHFAHCC_01688 | 1.2e-108 | S | Putative restriction endonuclease | |||
CNHFAHCC_01689 | 2.5e-120 | S | transposase or invertase | |||
CNHFAHCC_01690 | 0.0 | nuoM | 1.6.5.3 | C | NDH-1 shuttles electrons from NAD(P)H, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
CNHFAHCC_01691 | 2.7e-216 | G | Major facilitator superfamily | |||
CNHFAHCC_01692 | 2e-299 | crtD | Q | Flavin containing amine oxidoreductase | ||
CNHFAHCC_01693 | 1.8e-41 | ylmG | S | YGGT family | ||
CNHFAHCC_01694 | 2.4e-203 | futA1 | P | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_01695 | 2.6e-129 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
CNHFAHCC_01696 | 1.8e-23 | |||||
CNHFAHCC_01697 | 9.9e-205 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
CNHFAHCC_01698 | 0.0 | S | Fusaric acid resistance protein-like | |||
CNHFAHCC_01699 | 1.7e-66 | psbU | L | Stabilizes the structure of photosystem II oxygen- evolving complex (OEC), the ion environment of oxygen evolution and protects the OEC against heat-induced inactivation | ||
CNHFAHCC_01700 | 6.1e-93 | mcrA | V | HNH endonuclease | ||
CNHFAHCC_01701 | 2.6e-15 | |||||
CNHFAHCC_01702 | 3.7e-257 | ugd | 1.1.1.22 | M | UDP binding domain | |
CNHFAHCC_01703 | 1.1e-242 | ubiH | CH | FAD binding domain | ||
CNHFAHCC_01704 | 3.1e-69 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
CNHFAHCC_01705 | 3.2e-38 | S | Pfam:DUF1049 | |||
CNHFAHCC_01706 | 5e-30 | |||||
CNHFAHCC_01707 | 3.9e-149 | 3.4.21.72 | D | nuclear chromosome segregation | ||
CNHFAHCC_01708 | 9.1e-225 | cupB | C | CO2 hydration protein (ChpXY) | ||
CNHFAHCC_01709 | 9.2e-252 | egtB | 1.14.99.50, 2.7.11.1 | S | Sulfatase-modifying factor enzyme 1 | |
CNHFAHCC_01710 | 5.6e-255 | glcE | 1.1.3.15 | C | FAD binding domain | |
CNHFAHCC_01711 | 0.0 | actA | T | Putative diguanylate phosphodiesterase | ||
CNHFAHCC_01712 | 1.4e-278 | era | S | Domain of unknown function (DUF697) | ||
CNHFAHCC_01713 | 3.6e-93 | MA20_39615 | S | Cupin superfamily (DUF985) | ||
CNHFAHCC_01714 | 6e-165 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
CNHFAHCC_01715 | 8.2e-122 | S | Putative restriction endonuclease | |||
CNHFAHCC_01716 | 1.1e-208 | hemF | 1.3.3.3 | H | Involved in the heme and chlorophyll biosynthesis. Catalyzes the aerobic oxidative decarboxylation of propionate groups of rings A and B of coproporphyrinogen-III to yield the vinyl groups in protoporphyrinogen-IX | |
CNHFAHCC_01717 | 4.8e-131 | hmuO | 1.14.15.20 | P | Heme oxygenase | |
CNHFAHCC_01718 | 2.8e-113 | |||||
CNHFAHCC_01719 | 1.3e-37 | rpmB | J | Ribosomal L28 family | ||
CNHFAHCC_01720 | 6.7e-193 | S | Ycf66 protein N-terminus | |||
CNHFAHCC_01722 | 2.1e-125 | |||||
CNHFAHCC_01723 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | C | Belongs to the nitrite and sulfite reductase 4Fe-4S domain family | |
CNHFAHCC_01724 | 6.2e-115 | P | Iron permease FTR1 family | |||
CNHFAHCC_01725 | 5.1e-215 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
CNHFAHCC_01726 | 4.3e-141 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
CNHFAHCC_01727 | 1.4e-19 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_01728 | 8e-61 | S | Protein of unknown function (DUF1622) | |||
CNHFAHCC_01729 | 1e-223 | dapL | 2.6.1.83 | E | Aminotransferase class I and II | |
CNHFAHCC_01730 | 2.1e-51 | S | Bacterial SH3 domain | |||
CNHFAHCC_01731 | 2.2e-295 | ubiD | 4.1.1.61, 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
CNHFAHCC_01732 | 0.0 | cobJ | 2.1.1.130, 2.1.1.131, 2.1.1.133, 2.1.1.271, 2.6.1.9, 3.7.1.12 | H | Cobalamin synthesis G N-terminal | |
CNHFAHCC_01733 | 5.5e-237 | S | Domain of unknown function (DUF4335) | |||
CNHFAHCC_01734 | 7.4e-181 | aroF | 2.5.1.54 | E | NeuB family | |
CNHFAHCC_01735 | 2.9e-76 | S | Protein of unknown function (DUF3464) | |||
CNHFAHCC_01736 | 3.9e-41 | rpsO | J | Ribosomal_S15 | ||
CNHFAHCC_01737 | 1.8e-176 | ycgR | S | Predicted permease | ||
CNHFAHCC_01738 | 1.3e-79 | S | Tetratricopeptide repeat | |||
CNHFAHCC_01739 | 1e-87 | |||||
CNHFAHCC_01740 | 9.3e-86 | apcD | O | Phycobilisome protein | ||
CNHFAHCC_01741 | 2.9e-232 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
CNHFAHCC_01742 | 3.6e-193 | dusA | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines. Specifically modifies U20 and U20a in tRNAs | ||
CNHFAHCC_01743 | 8.5e-113 | S | Putative restriction endonuclease | |||
CNHFAHCC_01744 | 1.1e-92 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
CNHFAHCC_01745 | 4e-153 | yaaW | S | COGs COG4735 conserved | ||
CNHFAHCC_01746 | 1.8e-101 | S | Uncharacterized metal-binding protein (DUF2227) | |||
CNHFAHCC_01748 | 0.0 | epsB | 2.7.10.2 | D | Chain length determinant protein | |
CNHFAHCC_01749 | 5.6e-127 | S | Putative restriction endonuclease | |||
CNHFAHCC_01750 | 1.2e-152 | U | ABC-2 type transporter | |||
CNHFAHCC_01751 | 7.5e-23 | |||||
CNHFAHCC_01752 | 5.9e-76 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_01753 | 6.7e-104 | S | Putative restriction endonuclease | |||
CNHFAHCC_01754 | 9.9e-252 | 3.6.3.38 | GM | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_01755 | 1.6e-153 | rfbF | 2.7.7.33 | JM | MobA-like NTP transferase domain | |
CNHFAHCC_01756 | 3e-209 | rfbG | 4.2.1.45 | GM | RmlD substrate binding domain | |
CNHFAHCC_01757 | 5.8e-108 | rfbC | 5.1.3.13 | M | dTDP-4-dehydrorhamnose 3,5-epimerase | |
CNHFAHCC_01758 | 5.9e-238 | tpm | 2.1.1.67 | Q | C-methyltransferase C-terminal domain | |
CNHFAHCC_01759 | 8.9e-83 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_01760 | 2.7e-120 | S | Putative restriction endonuclease | |||
CNHFAHCC_01761 | 3.4e-106 | S | Putative restriction endonuclease | |||
CNHFAHCC_01762 | 5e-53 | S | Protein of unknown function (DUF2442) | |||
CNHFAHCC_01763 | 1.2e-221 | rfbE | 2.6.1.102 | M | DegT/DnrJ/EryC1/StrS aminotransferase family | |
CNHFAHCC_01764 | 1.6e-191 | 6.3.5.5 | S | ATP-grasp domain | ||
CNHFAHCC_01765 | 8e-235 | 4.1.1.35, 4.2.1.46, 5.1.3.2, 5.1.3.6 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
CNHFAHCC_01766 | 2.3e-150 | H | Methyltransferase domain | |||
CNHFAHCC_01767 | 1.1e-141 | V | Cephalosporin hydroxylase | |||
CNHFAHCC_01768 | 5.8e-21 | |||||
CNHFAHCC_01769 | 1.2e-58 | T | Toxic component of a toxin-antitoxin (TA) module | |||
CNHFAHCC_01770 | 0.0 | M | Glycosyl transferase, family 2 | |||
CNHFAHCC_01771 | 3.1e-214 | GT4 | M | Glycosyl transferases group 1 | ||
CNHFAHCC_01772 | 4e-214 | M | glycosyl transferase | |||
CNHFAHCC_01773 | 1.5e-233 | 2.4.1.11 | GT3 | M | Glycosyl transferases group 1 | |
CNHFAHCC_01774 | 3e-195 | galE | 5.1.3.2 | M | RmlD substrate binding domain | |
CNHFAHCC_01775 | 7.4e-08 | Q | methyltransferase activity | |||
CNHFAHCC_01777 | 1.5e-168 | pssJ | 2.7.8.20 | M | Glycosyl transferase family 2 | |
CNHFAHCC_01778 | 1.7e-156 | 2.1.1.222, 2.1.1.64 | H | Nodulation protein S (NodS) | ||
CNHFAHCC_01779 | 4.4e-180 | yefA | 4.2.1.47 | M | GDP-mannose 4,6 dehydratase | |
CNHFAHCC_01780 | 2.1e-221 | GT2,GT4 | M | PFAM Glycosyl transferase, group 1 | ||
CNHFAHCC_01782 | 4.6e-157 | L | Transposase | |||
CNHFAHCC_01783 | 1.2e-224 | pimB | 2.4.1.346 | GT4 | M | Glycosyltransferase Family 4 |
CNHFAHCC_01784 | 9.9e-227 | bme6 | 2.4.1.52 | GT4 | M | Glycosyl transferase 4-like domain |
CNHFAHCC_01785 | 8.1e-41 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
CNHFAHCC_01786 | 1.6e-35 | N | Periplasmic or secreted lipoprotein | |||
CNHFAHCC_01787 | 2.2e-56 | galE | 5.1.3.2 | M | RmlD substrate binding domain | |
CNHFAHCC_01788 | 5.8e-51 | |||||
CNHFAHCC_01789 | 9e-26 | |||||
CNHFAHCC_01790 | 3.2e-29 | S | conserved small protein | |||
CNHFAHCC_01791 | 1.3e-116 | S | Putative restriction endonuclease | |||
CNHFAHCC_01792 | 2.6e-49 | |||||
CNHFAHCC_01793 | 7.9e-102 | S | Putative restriction endonuclease | |||
CNHFAHCC_01794 | 1e-78 | wcaF | 2.3.1.79 | S | PFAM Bacterial transferase hexapeptide (three repeats) | |
CNHFAHCC_01795 | 1.4e-242 | wbjE | M | Glycosyl transferase 4-like domain | ||
CNHFAHCC_01796 | 3.1e-204 | S | Esterase-like activity of phytase | |||
CNHFAHCC_01797 | 7.4e-222 | E | FAD dependent oxidoreductase | |||
CNHFAHCC_01798 | 2.8e-42 | S | Belongs to the UPF0367 family | |||
CNHFAHCC_01799 | 1.1e-156 | yneE | S | Bestrophin, RFP-TM, chloride channel | ||
CNHFAHCC_01800 | 7.8e-227 | sucC | 6.2.1.5 | C | ATP-grasp domain | |
CNHFAHCC_01801 | 3.7e-123 | terC | P | Integral membrane protein TerC family | ||
CNHFAHCC_01802 | 9e-252 | S | Flotillin | |||
CNHFAHCC_01803 | 3.5e-162 | M | Glycosyl transferase family 2 | |||
CNHFAHCC_01804 | 4e-209 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
CNHFAHCC_01805 | 7.3e-25 | hli3 | S | PFAM Chlorophyll A-B binding protein | ||
CNHFAHCC_01806 | 6.3e-153 | gloB | 3.1.2.6 | S | Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid | |
CNHFAHCC_01807 | 5.2e-264 | pyrC | 3.5.2.3 | F | TIGRFAM dihydroorotase, multifunctional complex type | |
CNHFAHCC_01808 | 4.6e-252 | amtB | U | Ammonium Transporter Family | ||
CNHFAHCC_01809 | 3.1e-217 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_01810 | 2.7e-160 | uspA | T | Universal stress protein family | ||
CNHFAHCC_01811 | 0.0 | L | pilus organization | |||
CNHFAHCC_01812 | 0.0 | 3.1.3.1, 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
CNHFAHCC_01813 | 7.5e-97 | cysC | 1.8.4.10, 1.8.4.8, 2.7.1.25, 2.7.7.4 | F | Catalyzes the synthesis of activated sulfate | |
CNHFAHCC_01814 | 5.8e-118 | exbB | U | MotA/TolQ/ExbB proton channel family | ||
CNHFAHCC_01815 | 1.2e-135 | exbD | U | Biopolymer transport protein ExbD/TolR | ||
CNHFAHCC_01816 | 2.9e-262 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
CNHFAHCC_01817 | 3e-72 | djlA | O | PFAM Tellurite resistance protein TerB | ||
CNHFAHCC_01818 | 3.1e-137 | yrbG | P | Sodium/calcium exchanger protein | ||
CNHFAHCC_01819 | 2.6e-233 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
CNHFAHCC_01820 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_01821 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_01822 | 3e-133 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_01823 | 8.4e-172 | wecA | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
CNHFAHCC_01824 | 5.9e-151 | rnaZ | 3.1.26.11 | S | Beta-lactamase superfamily domain | |
CNHFAHCC_01825 | 0.0 | cya2 | 4.6.1.1 | T | CHASE2 | |
CNHFAHCC_01826 | 9e-142 | S | Domain of Unknown Function (DUF928) | |||
CNHFAHCC_01827 | 5.9e-188 | 3.1.1.83 | I | Steryl acetyl hydrolase | ||
CNHFAHCC_01828 | 2.9e-52 | S | Domain of unknown function (DUF4870) | |||
CNHFAHCC_01829 | 4.8e-111 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
CNHFAHCC_01830 | 3.5e-274 | cph2 | T | diguanylate cyclase | ||
CNHFAHCC_01831 | 3.7e-298 | |||||
CNHFAHCC_01832 | 0.0 | citT | U | Sodium:sulfate symporter transmembrane region | ||
CNHFAHCC_01833 | 2.1e-196 | csaB | S | Polysaccharide pyruvyl transferase | ||
CNHFAHCC_01834 | 8e-31 | S | Protein of unknown function (DUF2949) | |||
CNHFAHCC_01835 | 4.7e-232 | S | Homocysteine biosynthesis enzyme, sulfur-incorporation | |||
CNHFAHCC_01836 | 8.1e-235 | 2.7.7.72, 3.1.13.3, 3.1.3.7 | S | PFAM DHH family | ||
CNHFAHCC_01837 | 2.7e-255 | U | CHAT domain | |||
CNHFAHCC_01838 | 0.0 | ycf45 | S | Putative single-stranded nucleic acids-binding domain | ||
CNHFAHCC_01839 | 1e-190 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
CNHFAHCC_01840 | 2.7e-155 | btpA | S | BtpA family | ||
CNHFAHCC_01842 | 1e-90 | |||||
CNHFAHCC_01843 | 3.7e-165 | T | ATPase activity | |||
CNHFAHCC_01844 | 8.8e-228 | selD | 2.7.9.3 | C | Pyridine nucleotide-disulphide oxidoreductase | |
CNHFAHCC_01845 | 1.1e-172 | 5.4.99.23 | J | S4 RNA-binding domain | ||
CNHFAHCC_01846 | 2.2e-173 | T | Putative diguanylate phosphodiesterase | |||
CNHFAHCC_01847 | 8.9e-220 | cheV | T | cheY-homologous receiver domain | ||
CNHFAHCC_01848 | 2.3e-213 | nhaS4 | P | Sodium/hydrogen exchanger family | ||
CNHFAHCC_01849 | 0.0 | uvrD2 | L | DNA helicase | ||
CNHFAHCC_01850 | 2.5e-234 | pcxA | U | Involved in light-induced Na( )-dependent proton extrusion. Also seems to be involved in CO(2) transport | ||
CNHFAHCC_01851 | 2.1e-76 | S | Domain of unknown function (DUF4278) | |||
CNHFAHCC_01852 | 5.7e-166 | soj1 | D | AAA domain | ||
CNHFAHCC_01853 | 2.7e-76 | O | Hsp20/alpha crystallin family | |||
CNHFAHCC_01855 | 1.4e-184 | ccsA | U | Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment | ||
CNHFAHCC_01856 | 2.1e-75 | K | HxlR-like helix-turn-helix | |||
CNHFAHCC_01857 | 3.9e-167 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
CNHFAHCC_01858 | 9.3e-107 | S | Bacterial transferase hexapeptide (six repeats) | |||
CNHFAHCC_01859 | 3.9e-144 | I | Fatty acid hydroxylase superfamily | |||
CNHFAHCC_01860 | 2.6e-55 | ycf20 | S | Protein of unknown function (DUF565) | ||
CNHFAHCC_01861 | 1.5e-135 | nnrU | S | Phospholipid methyltransferase | ||
CNHFAHCC_01862 | 6e-31 | S | YlqD protein | |||
CNHFAHCC_01864 | 3.1e-60 | |||||
CNHFAHCC_01865 | 3.1e-159 | lpxC | 3.5.1.108, 4.2.1.59 | M | Catalyzes the hydrolysis of UDP-3-O-myristoyl-N- acetylglucosamine to form UDP-3-O-myristoylglucosamine and acetate, the committed step in lipid A biosynthesis | |
CNHFAHCC_01866 | 8.6e-93 | S | Alpha/beta hydrolase of unknown function (DUF1400) | |||
CNHFAHCC_01867 | 5.3e-213 | 4.2.2.26 | S | Heparinase II/III-like protein | ||
CNHFAHCC_01868 | 0.0 | ftsH2 | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
CNHFAHCC_01870 | 2.1e-41 | L | Transposase | |||
CNHFAHCC_01871 | 5.8e-39 | vapC | S | COGs COG1487 nucleic acid-binding protein contains PIN domain | ||
CNHFAHCC_01872 | 7.8e-35 | vapB | S | Virulence associated protein B | ||
CNHFAHCC_01873 | 2.3e-36 | S | TIGRFAM addiction module toxin, RelE StbE family | |||
CNHFAHCC_01874 | 5.5e-30 | |||||
CNHFAHCC_01875 | 9e-56 | S | Protein of unknown function DUF86 | |||
CNHFAHCC_01876 | 9.5e-52 | S | Nucleotidyltransferase domain | |||
CNHFAHCC_01877 | 4.5e-296 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
CNHFAHCC_01878 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | GXGXG motif | |
CNHFAHCC_01879 | 3.7e-23 | D | protein conserved in cyanobacteria | |||
CNHFAHCC_01880 | 4.2e-39 | D | protein conserved in cyanobacteria | |||
CNHFAHCC_01881 | 4.3e-244 | G | Glucose / Sorbosone dehydrogenase | |||
CNHFAHCC_01882 | 1.9e-288 | cbiA | 6.3.5.10, 6.3.5.11, 6.3.5.9 | F | Catalyzes the ATP-dependent amidation of the two carboxylate groups at positions a and c of cobyrinate, using either L-glutamine or ammonia as the nitrogen source | |
CNHFAHCC_01883 | 1.1e-206 | cobT | 2.4.2.21 | H | Belongs to the UPF0284 family | |
CNHFAHCC_01884 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
CNHFAHCC_01885 | 1.7e-226 | KT | Domain of unknown function (DUF4388) | |||
CNHFAHCC_01886 | 3.7e-81 | KT | cheY-homologous receiver domain | |||
CNHFAHCC_01887 | 2.6e-100 | cheW | NT | Two component signalling adaptor domain | ||
CNHFAHCC_01888 | 0.0 | ctr1 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | ||
CNHFAHCC_01889 | 1.5e-138 | ttg2B | U | Permease MlaE | ||
CNHFAHCC_01890 | 8.9e-60 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
CNHFAHCC_01891 | 6e-263 | 3.1.3.3 | T | GAF domain | ||
CNHFAHCC_01893 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
CNHFAHCC_01894 | 3.6e-47 | O | DnaJ molecular chaperone homology domain | |||
CNHFAHCC_01895 | 9.8e-22 | rpmF | J | Ribosomal L32p protein family | ||
CNHFAHCC_01896 | 7e-283 | pmt | 2.4.1.109 | GT39 | O | C-terminal four TMM region of protein-O-mannosyltransferase |
CNHFAHCC_01897 | 2e-143 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl-(Acyl carrier protein) reductase | |
CNHFAHCC_01898 | 7.7e-91 | S | SPTR Alr1246 protein | |||
CNHFAHCC_01899 | 9.8e-141 | S | Protein of unknown function (DUF2993) | |||
CNHFAHCC_01900 | 2.2e-185 | frpC | Q | Haemolysin-type calcium-binding repeat (2 copies) | ||
CNHFAHCC_01901 | 0.0 | bchH | 6.6.1.1, 6.6.1.2 | H | Domain of unknown function (DUF3479) | |
CNHFAHCC_01902 | 0.0 | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | |||
CNHFAHCC_01903 | 1.4e-190 | |||||
CNHFAHCC_01904 | 4.1e-147 | mazG | 3.6.1.66, 3.6.1.9 | S | MazG nucleotide pyrophosphohydrolase domain | |
CNHFAHCC_01905 | 8e-224 | 2.4.1.83, 2.7.8.12 | GT2 | M | Glycosyl transferase family group 2 | |
CNHFAHCC_01906 | 0.0 | T | PAS fold | |||
CNHFAHCC_01907 | 4.3e-26 | L | Putative transposase of IS4/5 family (DUF4096) | |||
CNHFAHCC_01908 | 5.4e-227 | ycf22 | Q | MlaD protein | ||
CNHFAHCC_01909 | 3.2e-144 | mkl | Q | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_01910 | 4.2e-43 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CNHFAHCC_01911 | 0.0 | U | haemagglutination activity domain | |||
CNHFAHCC_01912 | 4.5e-180 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
CNHFAHCC_01913 | 9.5e-97 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
CNHFAHCC_01914 | 2.2e-289 | glnA | 6.3.1.2 | E | Glutamine synthetase, catalytic domain | |
CNHFAHCC_01915 | 0.0 | T | CHASE | |||
CNHFAHCC_01916 | 4.1e-178 | T | diguanylate cyclase | |||
CNHFAHCC_01917 | 1.7e-105 | ytfC | 5.2.1.8 | O | FKBP-type peptidyl-prolyl cis-trans isomerase | |
CNHFAHCC_01918 | 7.7e-108 | ygfA | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
CNHFAHCC_01919 | 1.7e-123 | 3.1.3.18 | S | HAD-hyrolase-like | ||
CNHFAHCC_01920 | 1.2e-235 | S | Putative zinc binding domain | |||
CNHFAHCC_01921 | 9.1e-89 | |||||
CNHFAHCC_01922 | 7.9e-94 | terZ | T | TerD domain | ||
CNHFAHCC_01923 | 8.1e-284 | gadB | 4.1.1.15 | E | Pyridoxal-dependent decarboxylase conserved domain | |
CNHFAHCC_01924 | 6.5e-34 | S | Protein of unknown function (DUF433) | |||
CNHFAHCC_01925 | 1.8e-56 | S | protein conserved in bacteria | |||
CNHFAHCC_01926 | 9.2e-186 | ramA_1 | S | Carbon-nitrogen hydrolase | ||
CNHFAHCC_01927 | 9.8e-140 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
CNHFAHCC_01928 | 8.9e-75 | psbQ | S | TIGRFAM Photosystem II protein PsbQ | ||
CNHFAHCC_01929 | 2.3e-146 | O | prohibitin homologues | |||
CNHFAHCC_01930 | 1.7e-82 | yrdA | S | Bacterial transferase hexapeptide (six repeats) | ||
CNHFAHCC_01931 | 7.9e-60 | |||||
CNHFAHCC_01932 | 0.0 | S | X-Pro dipeptidyl-peptidase C-terminal non-catalytic domain | |||
CNHFAHCC_01933 | 2.4e-121 | thyX | 2.1.1.148 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor, and NADPH and FADH(2) as the reductant | |
CNHFAHCC_01934 | 2.2e-16 | psbK | U | One of the components of the core complex of photosystem II (PSII). PSII is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation | ||
CNHFAHCC_01935 | 2e-137 | 2.3.1.51 | I | Phosphate acyltransferases | ||
CNHFAHCC_01936 | 5e-38 | bolA | 6.3.5.3 | T | BolA-like protein | |
CNHFAHCC_01937 | 2.8e-54 | grxD | O | Glutaredoxin | ||
CNHFAHCC_01938 | 1.3e-52 | ybaB | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
CNHFAHCC_01939 | 3.9e-240 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
CNHFAHCC_01940 | 2.8e-293 | merA | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
CNHFAHCC_01941 | 2.4e-56 | |||||
CNHFAHCC_01942 | 0.0 | ureC | 3.5.1.5 | E | Urease alpha-subunit, N-terminal domain | |
CNHFAHCC_01943 | 9e-86 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_01944 | 4.9e-38 | |||||
CNHFAHCC_01945 | 5.7e-11 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_01946 | 4.3e-21 | |||||
CNHFAHCC_01947 | 0.0 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
CNHFAHCC_01948 | 4.1e-101 | ycf23 | 1.1.1.205, 1.13.12.16 | S | Protein of unknown function (DUF561) | |
CNHFAHCC_01949 | 0.0 | dxs | 2.2.1.7 | F | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
CNHFAHCC_01950 | 2.3e-62 | rub | C | Rubredoxin | ||
CNHFAHCC_01951 | 6e-151 | ycf48 | S | The ortholog in A.thaliana is involved in photosystem II (PSII) assembly, but knockout of the corresponding gene in Synechoccus PCC 7002 has no effect on PSII activity | ||
CNHFAHCC_01952 | 6.6e-40 | psbE | C | Lumenal portion of Cytochrome b559, alpha (gene psbE) subunit | ||
CNHFAHCC_01953 | 1.3e-16 | psbF | A | This b-type cytochrome is tightly associated with the reaction center of photosystem II (PSII). PSII is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation | ||
CNHFAHCC_01954 | 7.5e-13 | psbL | U | One of the components of the core complex of photosystem II (PSII). PSII is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. This subunit is found at the monomer-monomer interface and is required for correct PSII assembly and or dimerization | ||
CNHFAHCC_01955 | 1.7e-12 | psbJ | U | (PSII) is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation | ||
CNHFAHCC_01956 | 3.9e-204 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
CNHFAHCC_01957 | 8e-24 | L | transposition | |||
CNHFAHCC_01958 | 4.6e-12 | L | Putative transposase of IS4/5 family (DUF4096) | |||
CNHFAHCC_01959 | 8.4e-190 | L | PFAM Transposase | |||
CNHFAHCC_01960 | 7.1e-161 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
CNHFAHCC_01961 | 3.5e-120 | S | Putative restriction endonuclease | |||
CNHFAHCC_01962 | 5.6e-111 | pilP | NU | Pilus assembly protein, PilP | ||
CNHFAHCC_01963 | 0.0 | gyrA | 5.99.1.3 | L | DNA gyrase/topoisomerase IV, subunit A | |
CNHFAHCC_01964 | 3.6e-67 | rpfC | 2.7.13.3 | T | cheY-homologous receiver domain | |
CNHFAHCC_01965 | 3.2e-163 | mtfA | S | Glucose-regulated metallo-peptidase M90 | ||
CNHFAHCC_01966 | 1.9e-83 | S | Bacterial pre-peptidase C-terminal domain | |||
CNHFAHCC_01967 | 2.5e-118 | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | |||
CNHFAHCC_01968 | 1.3e-32 | |||||
CNHFAHCC_01969 | 4.3e-112 | S | Putative restriction endonuclease | |||
CNHFAHCC_01970 | 2.5e-71 | zur | P | Ferric uptake regulator family | ||
CNHFAHCC_01971 | 3.6e-164 | znuA | 1.6.5.3 | P | Zinc-uptake complex component A periplasmic | |
CNHFAHCC_01972 | 2.1e-165 | znuC | 3.6.3.34 | P | AAA domain, putative AbiEii toxin, Type IV TA system | |
CNHFAHCC_01973 | 1.2e-133 | znuB | U | ABC 3 transport family | ||
CNHFAHCC_01974 | 9.5e-46 | Q | calcium- and calmodulin-responsive adenylate cyclase activity | |||
CNHFAHCC_01975 | 0.0 | mshQ | QU | Cadherin repeats. | ||
CNHFAHCC_01976 | 2.4e-181 | phoH | T | PhoH-like protein | ||
CNHFAHCC_01977 | 2.6e-158 | S | Tetratricopeptide repeat | |||
CNHFAHCC_01978 | 1.4e-109 | ycf58 | E | Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins | ||
CNHFAHCC_01979 | 5e-139 | cpcG | 2.7.7.24 | G | Phycobilisome Linker polypeptide | |
CNHFAHCC_01980 | 1.2e-163 | |||||
CNHFAHCC_01981 | 8.8e-83 | |||||
CNHFAHCC_01982 | 7.9e-165 | I | alpha/beta hydrolase fold | |||
CNHFAHCC_01983 | 7.2e-172 | dnaJ3 | J | DnaJ C terminal domain | ||
CNHFAHCC_01984 | 0.0 | dnaK | O | MreB/Mbl protein | ||
CNHFAHCC_01985 | 7.3e-247 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
CNHFAHCC_01986 | 3.7e-50 | L | IS1 transposase | |||
CNHFAHCC_01987 | 1.2e-88 | L | DDE superfamily endonuclease | |||
CNHFAHCC_01988 | 0.0 | comEC | S | Domain of unknown function (DUF4131) | ||
CNHFAHCC_01989 | 1.2e-111 | ectA | 2.3.1.178 | K | FR47-like protein | |
CNHFAHCC_01990 | 3.9e-75 | |||||
CNHFAHCC_01991 | 0.0 | M | Carbohydrate-selective porin, OprB family | |||
CNHFAHCC_01992 | 2.7e-117 | narL | KT | helix_turn_helix, Lux Regulon | ||
CNHFAHCC_01993 | 2.2e-190 | amiC | 3.5.1.28 | M | Ami_3 | |
CNHFAHCC_01994 | 1.5e-79 | |||||
CNHFAHCC_01995 | 3.4e-79 | S | Protein of unknown function (DUF1036) | |||
CNHFAHCC_01996 | 1.1e-56 | T | STAS domain | |||
CNHFAHCC_01997 | 3.2e-59 | |||||
CNHFAHCC_01998 | 2e-61 | |||||
CNHFAHCC_01999 | 1.5e-138 | M | Curli production assembly/transport component CsgG | |||
CNHFAHCC_02000 | 4.9e-72 | S | PFAM TM2 domain | |||
CNHFAHCC_02001 | 8.2e-51 | S | Domain of unknown function (DUF1825) | |||
CNHFAHCC_02002 | 1e-164 | pcaD | 2.3.1.20, 3.1.1.24, 3.1.1.76, 4.1.1.44 | S | Serine aminopeptidase, S33 | |
CNHFAHCC_02003 | 8.9e-183 | acoC | 2.3.1.12 | I | Serine aminopeptidase, S33 | |
CNHFAHCC_02004 | 2e-109 | O | Protein CHAPERONE-LIKE PROTEIN OF POR1-like | |||
CNHFAHCC_02005 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein dimerisation domain | |
CNHFAHCC_02006 | 5.3e-75 | T | Histidine kinase | |||
CNHFAHCC_02007 | 4.2e-269 | glcF | C | 4Fe-4S dicluster domain | ||
CNHFAHCC_02008 | 1.4e-198 | J | translation release factor activity | |||
CNHFAHCC_02009 | 0.0 | aarF | S | ABC1 family | ||
CNHFAHCC_02010 | 4.2e-211 | |||||
CNHFAHCC_02011 | 1.8e-187 | rbcR | K | LysR substrate binding domain | ||
CNHFAHCC_02012 | 4e-27 | gifA | ||||
CNHFAHCC_02013 | 3.9e-178 | phzF | 5.3.3.17 | S | Phenazine biosynthesis-like protein | |
CNHFAHCC_02015 | 2.4e-200 | S | Wd-40 repeat | |||
CNHFAHCC_02016 | 1.7e-159 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
CNHFAHCC_02017 | 2e-94 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
CNHFAHCC_02018 | 1.1e-230 | sqdB | 3.13.1.1 | GM | GDP-mannose 4,6 dehydratase | |
CNHFAHCC_02019 | 4.3e-46 | P | Protein of unknown function (DUF2470) | |||
CNHFAHCC_02020 | 5.7e-113 | S | Putative restriction endonuclease | |||
CNHFAHCC_02021 | 1.8e-109 | S | Protein of unknown function (DUF1449) | |||
CNHFAHCC_02022 | 5.2e-201 | kch | P | Ion channel | ||
CNHFAHCC_02023 | 1.1e-247 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
CNHFAHCC_02024 | 3.4e-57 | 1.13.11.4, 5.3.1.15 | S | Cupin domain | ||
CNHFAHCC_02025 | 3.3e-115 | S | PAP_fibrillin | |||
CNHFAHCC_02026 | 1.1e-24 | |||||
CNHFAHCC_02027 | 7.4e-168 | fghA | 3.1.2.12 | CE1 | S | Putative esterase |
CNHFAHCC_02028 | 1.7e-215 | adhC | 1.1.1.1, 1.1.1.284 | C | Zinc-binding dehydrogenase | |
CNHFAHCC_02030 | 0.0 | Q | Domain of unknown function (DUF4114) | |||
CNHFAHCC_02031 | 1.1e-198 | chlI | 6.6.1.1 | H | magnesium ion into protoporphyrin IX to yield | |
CNHFAHCC_02032 | 7.4e-233 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
CNHFAHCC_02033 | 4.4e-61 | S | PFAM DsrE DsrF-like family | |||
CNHFAHCC_02034 | 0.0 | L | helicase activity | |||
CNHFAHCC_02035 | 5.6e-36 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
CNHFAHCC_02036 | 1.8e-68 | ycf41 | L | Single-strand binding protein family | ||
CNHFAHCC_02037 | 1.3e-96 | |||||
CNHFAHCC_02038 | 1.5e-67 | L | COGs COG3677 Transposase and inactivated derivatives | |||
CNHFAHCC_02039 | 0.0 | ybiO | M | Mechanosensitive ion channel | ||
CNHFAHCC_02040 | 2e-82 | 4.4.1.5, 5.1.99.1 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
CNHFAHCC_02041 | 4.3e-65 | KT | cheY-homologous receiver domain | |||
CNHFAHCC_02042 | 6.5e-157 | mnmC | 2.1.1.61, 2.1.1.72, 2.4.2.29, 4.2.1.151 | S | S-adenosyl-L-methionine-dependent methyltransferase | |
CNHFAHCC_02043 | 4.7e-64 | S | granule-associated protein | |||
CNHFAHCC_02044 | 9.2e-89 | |||||
CNHFAHCC_02045 | 1.2e-219 | rnhA | 3.1.26.4 | L | Reverse transcriptase-like | |
CNHFAHCC_02046 | 6.8e-122 | Q | Putative RNA methylase family UPF0020 | |||
CNHFAHCC_02047 | 6.8e-56 | |||||
CNHFAHCC_02048 | 7.5e-123 | lepB | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
CNHFAHCC_02049 | 2.6e-117 | S | Putative restriction endonuclease | |||
CNHFAHCC_02050 | 1.1e-278 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
CNHFAHCC_02051 | 1.2e-180 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
CNHFAHCC_02052 | 1.5e-115 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
CNHFAHCC_02053 | 4.6e-238 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
CNHFAHCC_02054 | 1.4e-138 | clcD | 3.1.1.45 | Q | Dienelactone hydrolase family | |
CNHFAHCC_02056 | 1.1e-86 | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | |||
CNHFAHCC_02058 | 5.3e-228 | S | protein conserved in bacteria | |||
CNHFAHCC_02059 | 2.8e-182 | devS | 2.7.13.3 | T | GAF domain | |
CNHFAHCC_02060 | 3.1e-43 | |||||
CNHFAHCC_02061 | 2.1e-204 | pobA | P | Rieske [2Fe-2S] domain | ||
CNHFAHCC_02062 | 1.5e-49 | fdxC | 4.6.1.1 | C | 2Fe-2S iron-sulfur cluster binding domain | |
CNHFAHCC_02063 | 0.0 | pilL | 2.7.13.3 | NT | Signal transducing histidine kinase, homodimeric domain | |
CNHFAHCC_02064 | 0.0 | pilJ | 4.6.1.1 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |
CNHFAHCC_02065 | 1.6e-82 | cheW | NT | Two component signalling adaptor domain | ||
CNHFAHCC_02066 | 4.4e-64 | KT | cheY-homologous receiver domain | |||
CNHFAHCC_02067 | 3.7e-227 | KT | cheY-homologous receiver domain | |||
CNHFAHCC_02068 | 0.0 | rnb | 3.1.13.1 | J | RNB | |
CNHFAHCC_02069 | 6.9e-112 | O | Redoxin | |||
CNHFAHCC_02070 | 0.0 | ftsH4 | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
CNHFAHCC_02071 | 2.2e-84 | S | domain, Protein | |||
CNHFAHCC_02072 | 1.3e-35 | feoA | P | Fe2 transport system protein A | ||
CNHFAHCC_02073 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
CNHFAHCC_02074 | 4e-33 | S | PFAM Chlorophyll A-B binding protein | |||
CNHFAHCC_02075 | 0.0 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |||
CNHFAHCC_02076 | 1.1e-75 | yuiD | S | Divergent PAP2 family | ||
CNHFAHCC_02078 | 9.7e-115 | ycfA | K | Bacterial regulatory proteins, tetR family | ||
CNHFAHCC_02079 | 4.6e-210 | S | Glycosyl Transferase | |||
CNHFAHCC_02080 | 8.4e-116 | |||||
CNHFAHCC_02081 | 3.6e-114 | J | tRNA 5'-leader removal | |||
CNHFAHCC_02083 | 6.9e-178 | mqnC | 1.21.98.1, 2.5.1.120, 2.5.1.77, 4.1.99.19 | H | Catalyzes the radical-mediated transfer of the hydroxybenzyl group from 4-hydroxyphenylpyruvate (HPP) to 5-amino- 6-ribitylamino-2,4(1H,3H)-pyrimidinedione to form 7,8-didemethyl- 8-hydroxy-5-deazariboflavin (FO) | |
CNHFAHCC_02084 | 3e-113 | CP_0488 | S | Phospholipase/Carboxylesterase | ||
CNHFAHCC_02085 | 3.5e-216 | spoIID | D | Stage II sporulation protein | ||
CNHFAHCC_02086 | 2.1e-162 | S | Protein of unknown function (DUF1350) | |||
CNHFAHCC_02087 | 1.1e-76 | 6.6.1.2 | C | Ferredoxin | ||
CNHFAHCC_02088 | 1e-179 | recN | 6.5.1.2 | LNU | breast cancer carboxy-terminal domain | |
CNHFAHCC_02089 | 0.0 | 3.6.4.12 | L | AAA domain | ||
CNHFAHCC_02090 | 3.2e-278 | gumB | M | Polysaccharide biosynthesis/export protein | ||
CNHFAHCC_02091 | 1.8e-46 | S | Tryptophan-rich protein (DUF2389) | |||
CNHFAHCC_02092 | 4.1e-133 | S | Domain of unknown function (DUF1995) | |||
CNHFAHCC_02093 | 3.3e-247 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
CNHFAHCC_02094 | 3.4e-39 | boxA | 1.14.13.208, 1.18.1.2, 1.19.1.1 | P | CpcD/allophycocyanin linker domain | |
CNHFAHCC_02095 | 5.1e-159 | coaE | 2.7.1.24 | H | CpcD/allophycocyanin linker domain | |
CNHFAHCC_02096 | 5.5e-147 | coaE | 2.7.1.24 | H | CpcD/allophycocyanin linker domain | |
CNHFAHCC_02097 | 1.9e-86 | rpcA | C | Phycobilisome protein | ||
CNHFAHCC_02098 | 1.6e-88 | cpcB | C | Phycobilisome protein | ||
CNHFAHCC_02099 | 9.1e-33 | |||||
CNHFAHCC_02100 | 1e-148 | U | multi-organism process | |||
CNHFAHCC_02101 | 8.7e-30 | |||||
CNHFAHCC_02102 | 8.1e-243 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_02103 | 1.1e-50 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_02104 | 4.5e-71 | |||||
CNHFAHCC_02105 | 5.2e-164 | aspA | 3.5.1.15 | E | Succinylglutamate desuccinylase / Aspartoacylase family | |
CNHFAHCC_02106 | 5.1e-195 | dfrA | 1.1.1.219 | GM | Male sterility protein | |
CNHFAHCC_02107 | 1.8e-24 | copZ | P | Heavy-metal-associated domain | ||
CNHFAHCC_02108 | 2.9e-208 | M | Peptidase family M23 | |||
CNHFAHCC_02109 | 3.7e-257 | dnaE | 2.7.7.7 | L | Helix-hairpin-helix motif | |
CNHFAHCC_02110 | 2.1e-142 | S | RDD family | |||
CNHFAHCC_02111 | 1.9e-132 | G | transport | |||
CNHFAHCC_02112 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | MT | Inner membrane component of T3SS, cytoplasmic domain |
CNHFAHCC_02113 | 7e-104 | S | PAP_fibrillin | |||
CNHFAHCC_02114 | 0.0 | gsiA | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
CNHFAHCC_02115 | 8.8e-73 | rpaC | ||||
CNHFAHCC_02116 | 1.1e-147 | S | Beta-lactamase superfamily domain | |||
CNHFAHCC_02117 | 5.5e-121 | Z012_00420 | S | Uncharacterized integral membrane protein (DUF2301) | ||
CNHFAHCC_02118 | 1.3e-52 | P | NADH-ubiquinone/plastoquinone oxidoreductase chain 4L | |||
CNHFAHCC_02119 | 1.8e-265 | ndhD5 | 1.6.5.3 | CP | Proton-conducting membrane transporter | |
CNHFAHCC_02120 | 1.8e-54 | P | NADH-ubiquinone/plastoquinone oxidoreductase chain 4L | |||
CNHFAHCC_02121 | 9.3e-262 | nuoM2 | 1.6.5.3 | CP | Proton-conducting membrane transporter | |
CNHFAHCC_02122 | 8.3e-69 | mrpE | P | Na+/H+ ion antiporter subunit | ||
CNHFAHCC_02123 | 1.8e-32 | |||||
CNHFAHCC_02124 | 3e-47 | P | Na+/H+ antiporter subunit | |||
CNHFAHCC_02125 | 4e-96 | P | Domain of unknown function (DUF4040) | |||
CNHFAHCC_02126 | 3e-108 | P | Domain related to MnhB subunit of Na+/H+ antiporter | |||
CNHFAHCC_02127 | 4.5e-244 | S | Protein of unknown function DUF58 | |||
CNHFAHCC_02128 | 4.9e-131 | crp1 | K | helix_turn_helix, cAMP Regulatory protein | ||
CNHFAHCC_02129 | 1.4e-142 | comGD | NU | Prokaryotic N-terminal methylation motif | ||
CNHFAHCC_02130 | 3.2e-83 | lspI | NU | Prokaryotic N-terminal methylation motif | ||
CNHFAHCC_02131 | 5.6e-200 | NU | pilus assembly protein PilW | |||
CNHFAHCC_02132 | 0.0 | NU | Pilus assembly protein PilX | |||
CNHFAHCC_02133 | 0.0 | V | ABC transporter transmembrane region | |||
CNHFAHCC_02134 | 1.6e-137 | S | Tetratricopeptide repeat | |||
CNHFAHCC_02135 | 0.0 | silP | 3.6.3.4, 3.6.3.54 | P | Heavy-metal-associated domain | |
CNHFAHCC_02136 | 1.3e-162 | fabD | 2.3.1.39 | I | Acyl transferase domain | |
CNHFAHCC_02137 | 6.3e-91 | T | cheY-homologous receiver domain | |||
CNHFAHCC_02138 | 4.9e-81 | S | Putative bacterial sensory transduction regulator | |||
CNHFAHCC_02139 | 1e-245 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
CNHFAHCC_02140 | 7.2e-112 | nadD | 2.7.7.18, 3.6.1.55 | F | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
CNHFAHCC_02141 | 5.8e-100 | E | lactoylglutathione lyase activity | |||
CNHFAHCC_02142 | 6.2e-165 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
CNHFAHCC_02143 | 1e-259 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
CNHFAHCC_02144 | 0.0 | C | FAD dependent oxidoreductase | |||
CNHFAHCC_02145 | 8e-45 | S | PIN domain | |||
CNHFAHCC_02147 | 2.3e-63 | |||||
CNHFAHCC_02148 | 0.0 | zam | J | Cold shock protein domain | ||
CNHFAHCC_02149 | 4.5e-263 | C | Protein of unknown function (DUF512) | |||
CNHFAHCC_02150 | 2.9e-260 | rsbU | 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
CNHFAHCC_02151 | 1.5e-08 | |||||
CNHFAHCC_02152 | 3.1e-259 | argH | 4.3.2.1 | E | Argininosuccinate lyase C-terminal | |
CNHFAHCC_02153 | 7.2e-77 | nudF | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
CNHFAHCC_02154 | 0.0 | S | KAP family P-loop domain | |||
CNHFAHCC_02155 | 0.0 | C | Uncharacterized protein conserved in bacteria (DUF2344) | |||
CNHFAHCC_02156 | 4e-184 | coxM | 1.9.3.1 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
CNHFAHCC_02157 | 0.0 | ctaD | 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
CNHFAHCC_02158 | 3.9e-113 | ctaE | 1.9.3.1 | C | Cytochrome c oxidase subunit III | |
CNHFAHCC_02159 | 1.8e-56 | trxA3 | O | Thioredoxin | ||
CNHFAHCC_02160 | 2.5e-219 | strS | M | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
CNHFAHCC_02161 | 8.8e-150 | tauB | P | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_02162 | 1.3e-148 | P | Binding-protein-dependent transport system inner membrane component | |||
CNHFAHCC_02163 | 1.1e-189 | P | NMT1/THI5 like | |||
CNHFAHCC_02164 | 3.3e-129 | hypB | KO | CobW/HypB/UreG, nucleotide-binding domain | ||
CNHFAHCC_02165 | 1e-65 | hypA | S | Probably plays a role in a hydrogenase nickel cofactor insertion step | ||
CNHFAHCC_02166 | 2.4e-233 | speB2 | 3.5.3.11 | E | Arginase family | |
CNHFAHCC_02167 | 3.1e-92 | T | GAF domain | |||
CNHFAHCC_02168 | 1.3e-190 | T | diguanylate cyclase | |||
CNHFAHCC_02169 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
CNHFAHCC_02170 | 2.2e-24 | |||||
CNHFAHCC_02171 | 0.0 | leuS | 6.1.1.4 | J | Leucyl-tRNA synthetase, Domain 2 | |
CNHFAHCC_02172 | 3.1e-215 | gltS | E | Catalyzes the sodium-dependent transport of glutamate | ||
CNHFAHCC_02173 | 5.8e-52 | S | Protein of unknown function (DUF3155) | |||
CNHFAHCC_02174 | 1.3e-235 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |||
CNHFAHCC_02175 | 1.5e-103 | FG | Domain of unknown function (DUF4269) | |||
CNHFAHCC_02176 | 0.0 | MdlB | V | ABC transporter transmembrane region | ||
CNHFAHCC_02177 | 1.1e-97 | |||||
CNHFAHCC_02178 | 2.2e-122 | S | Putative restriction endonuclease | |||
CNHFAHCC_02179 | 2.8e-159 | S | Alternative locus ID | |||
CNHFAHCC_02180 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
CNHFAHCC_02181 | 8.4e-240 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
CNHFAHCC_02182 | 9.8e-33 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
CNHFAHCC_02183 | 8.3e-78 | |||||
CNHFAHCC_02184 | 3.3e-39 | sipA | S | Protein of unknown function (DUF3148) | ||
CNHFAHCC_02185 | 7.9e-82 | bfr | 1.16.3.1 | P | Iron-storage protein, whose ferroxidase center binds Fe(2 ) ions, oxidizes them by dioxygen to Fe(3 ), and participates in the subsequent Fe(3 ) oxide mineral core formation within the central cavity of the protein complex | |
CNHFAHCC_02186 | 9.2e-104 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_02187 | 1.2e-61 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
CNHFAHCC_02188 | 1.4e-261 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
CNHFAHCC_02189 | 6.4e-08 | S | Protein of unknown function (DUF2949) | |||
CNHFAHCC_02190 | 2.1e-41 | rpmE | J | Ribosomal protein L31 | ||
CNHFAHCC_02191 | 1.4e-71 | rpsI | J | Ribosomal protein S9/S16 | ||
CNHFAHCC_02192 | 1e-81 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
CNHFAHCC_02193 | 4.5e-165 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
CNHFAHCC_02194 | 2.9e-57 | rplQ | J | Ribosomal protein L17 | ||
CNHFAHCC_02195 | 1.8e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_02196 | 8.1e-64 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
CNHFAHCC_02197 | 8.7e-63 | rpsM | J | Ribosomal protein S13/S18 | ||
CNHFAHCC_02198 | 7.8e-35 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
CNHFAHCC_02199 | 3.7e-102 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
CNHFAHCC_02200 | 4e-240 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
CNHFAHCC_02201 | 2e-74 | rplO | J | Ribosomal proteins 50S-L15, 50S-L18e, 60S-L27A | ||
CNHFAHCC_02202 | 8.4e-85 | rpsE | J | Belongs to the universal ribosomal protein uS5 family | ||
CNHFAHCC_02203 | 4.4e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
CNHFAHCC_02204 | 3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
CNHFAHCC_02205 | 4.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
CNHFAHCC_02206 | 3.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
CNHFAHCC_02207 | 7.6e-58 | rplX | J | Ribosomal proteins 50S L24/mitochondrial 39S L24 | ||
CNHFAHCC_02208 | 3.5e-61 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
CNHFAHCC_02209 | 4e-37 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
CNHFAHCC_02210 | 7.8e-32 | rpmC | J | Ribosomal L29 protein | ||
CNHFAHCC_02211 | 3.5e-73 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
CNHFAHCC_02212 | 1.7e-131 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
CNHFAHCC_02213 | 1.3e-60 | rplV | J | Ribosomal protein L22p/L17e | ||
CNHFAHCC_02214 | 3.5e-45 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
CNHFAHCC_02215 | 2e-152 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
CNHFAHCC_02216 | 2.4e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
CNHFAHCC_02217 | 5.8e-112 | rplD | J | Ribosomal protein L4/L1 family | ||
CNHFAHCC_02218 | 2.9e-79 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
CNHFAHCC_02219 | 4.2e-83 | dps | P | Ferritin-like domain | ||
CNHFAHCC_02220 | 2e-109 | ubiC | 4.1.3.40 | H | Protein of unknown function (DUF98) | |
CNHFAHCC_02221 | 1.6e-229 | S | Calcineurin-like phosphoesterase | |||
CNHFAHCC_02222 | 8e-72 | S | Domain of unknown function (DUF1823) | |||
CNHFAHCC_02223 | 4.5e-61 | petJ | C | Functions as an electron carrier between membrane-bound cytochrome b6-f and photosystem I in oxygenic photosynthesis | ||
CNHFAHCC_02224 | 3.6e-224 | srrA1 | G | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_02225 | 3.5e-163 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
CNHFAHCC_02226 | 4.4e-124 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
CNHFAHCC_02227 | 3.8e-139 | S | Protein of unknown function (DUF3386) | |||
CNHFAHCC_02228 | 4e-179 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
CNHFAHCC_02229 | 1.5e-79 | L | PFAM IS1 transposase | |||
CNHFAHCC_02230 | 4.4e-71 | L | PFAM transposase, IS4 family protein | |||
CNHFAHCC_02231 | 4.3e-70 | L | Putative transposase of IS4/5 family (DUF4096) | |||
CNHFAHCC_02232 | 0.0 | rpoC2 | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_02233 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_02234 | 1.7e-150 | dtd3 | L | TatD related DNase | ||
CNHFAHCC_02235 | 8.5e-42 | rpsT | J | Ribosomal protein S20 | ||
CNHFAHCC_02236 | 0.0 | 2.7.13.3 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | ||
CNHFAHCC_02237 | 1.8e-147 | |||||
CNHFAHCC_02238 | 0.0 | 3.1.11.5, 3.6.4.12 | L | UvrD-like helicase C-terminal domain | ||
CNHFAHCC_02239 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
CNHFAHCC_02240 | 2.1e-215 | hsK1 | S | Ecdysteroid kinase | ||
CNHFAHCC_02241 | 4.2e-129 | P | Mo-dependent nitrogenase C-terminus | |||
CNHFAHCC_02242 | 4.3e-88 | S | Protein of unknown function (DUF3531) | |||
CNHFAHCC_02243 | 1.4e-98 | S | Tetratricopeptide repeat | |||
CNHFAHCC_02244 | 1.7e-229 | ligA | 2.7.7.7, 6.5.1.2 | LU | DNA recombination-mediator protein A | |
CNHFAHCC_02245 | 2.2e-51 | S | Putative heavy-metal-binding | |||
CNHFAHCC_02246 | 1.2e-45 | S | Protein of unknown function (DUF2442) | |||
CNHFAHCC_02247 | 2.3e-121 | lsfA | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
CNHFAHCC_02248 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
CNHFAHCC_02249 | 7.1e-209 | urtB | E | Branched-chain amino acid transport system / permease component | ||
CNHFAHCC_02250 | 1.7e-229 | urtC | E | Branched-chain amino acid transport system / permease component | ||
CNHFAHCC_02251 | 1.8e-167 | lacF | G | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_02252 | 9.3e-77 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02253 | 9e-234 | htrA | 3.4.21.107 | O | Trypsin | |
CNHFAHCC_02254 | 8.8e-92 | ndoA | P | Rieske-like [2Fe-2S] domain | ||
CNHFAHCC_02255 | 2.3e-120 | L | Protein of unknown function (DUF1997) | |||
CNHFAHCC_02256 | 4e-199 | acrA | M | Barrel-sandwich domain of CusB or HlyD membrane-fusion | ||
CNHFAHCC_02257 | 2.1e-28 | |||||
CNHFAHCC_02258 | 0.0 | IQ | Class II Aldolase and Adducin N-terminal domain | |||
CNHFAHCC_02259 | 2e-55 | S | Protein of unknown function (DUF433) | |||
CNHFAHCC_02260 | 2.7e-67 | 1.17.4.1 | S | Mut7-C RNAse domain | ||
CNHFAHCC_02261 | 0.0 | cobN | 6.6.1.1, 6.6.1.2 | H | CobN/Magnesium Chelatase | |
CNHFAHCC_02262 | 0.0 | pdtaS | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_02263 | 1.7e-131 | phyR | K | helix_turn_helix, arabinose operon control protein | ||
CNHFAHCC_02264 | 1.2e-213 | patA | 2.7.13.3 | T | cheY-homologous receiver domain | |
CNHFAHCC_02265 | 1.2e-123 | slr1215 | ||||
CNHFAHCC_02266 | 5.9e-82 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
CNHFAHCC_02267 | 6.4e-16 | |||||
CNHFAHCC_02268 | 5.2e-206 | mgtE | P | MgtE intracellular N domain | ||
CNHFAHCC_02269 | 2.4e-239 | 2.4.1.11, 2.4.1.18 | GH57,GT4 | G | Glycosyl transferase 4-like | |
CNHFAHCC_02270 | 3.5e-151 | S | protein conserved in bacteria | |||
CNHFAHCC_02271 | 3.1e-53 | |||||
CNHFAHCC_02272 | 3.5e-114 | lip | 3.1.1.3 | S | Lipase (class 2) | |
CNHFAHCC_02273 | 5.8e-117 | pmgA | 2.7.11.1 | T | Histidine kinase-like ATPase domain | |
CNHFAHCC_02274 | 1.3e-270 | rumA | 2.1.1.190, 2.1.1.35 | J | tRNA (Uracil-5-)-methyltransferase | |
CNHFAHCC_02275 | 7e-297 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
CNHFAHCC_02276 | 5.5e-98 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
CNHFAHCC_02277 | 6.8e-71 | manA | 2.7.7.13, 5.3.1.8 | G | Mannose-6-phosphate isomerase | |
CNHFAHCC_02278 | 3.4e-31 | S | BrnA antitoxin of type II toxin-antitoxin system | |||
CNHFAHCC_02279 | 1.9e-43 | S | Ribonuclease toxin, BrnT, of type II toxin-antitoxin system | |||
CNHFAHCC_02280 | 4e-50 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
CNHFAHCC_02281 | 1.5e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
CNHFAHCC_02282 | 0.0 | T | Putative diguanylate phosphodiesterase | |||
CNHFAHCC_02284 | 3.7e-96 | 3.6.1.13 | L | pfam nudix | ||
CNHFAHCC_02285 | 6.1e-108 | S | Alternative locus ID | |||
CNHFAHCC_02286 | 1.3e-204 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
CNHFAHCC_02287 | 1.2e-48 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
CNHFAHCC_02288 | 4.3e-89 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
CNHFAHCC_02289 | 3.2e-127 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
CNHFAHCC_02290 | 3.3e-71 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
CNHFAHCC_02291 | 9.3e-115 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
CNHFAHCC_02292 | 2.4e-34 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
CNHFAHCC_02294 | 5.1e-60 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
CNHFAHCC_02295 | 1.4e-71 | |||||
CNHFAHCC_02296 | 4.6e-156 | acoC | 2.3.1.12, 3.8.1.5 | I | Serine aminopeptidase, S33 | |
CNHFAHCC_02297 | 6.3e-167 | S | Late competence development protein ComFB | |||
CNHFAHCC_02298 | 2.2e-128 | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | |||
CNHFAHCC_02299 | 1.3e-79 | ycf60 | S | Chloroplast import apparatus Tic20-like | ||
CNHFAHCC_02300 | 2.3e-53 | 1.18.1.3 | C | 2Fe-2S iron-sulfur cluster binding domain | ||
CNHFAHCC_02301 | 1.3e-190 | phaE | A | Poly(R)-hydroxyalkanoic acid synthase subunit (PHA_synth_III_E) | ||
CNHFAHCC_02302 | 1.2e-221 | phaC | I | Protein of unknown function (DUF3141) | ||
CNHFAHCC_02303 | 4.5e-67 | K | transcription initiation from RNA polymerase II promoter | |||
CNHFAHCC_02304 | 5.2e-66 | M | Four repeated domains in the Fasciclin I family of proteins, present in many other contexts. | |||
CNHFAHCC_02305 | 1.2e-260 | cupA | C | CO2 hydration protein (ChpXY) | ||
CNHFAHCC_02306 | 1.3e-274 | nuoM | 1.6.5.3 | C | Proton-conducting membrane transporter | |
CNHFAHCC_02307 | 0.0 | ndhF3 | 1.6.5.3 | CP | NADH-Ubiquinone oxidoreductase (complex I), chain 5 N-terminus | |
CNHFAHCC_02308 | 2.5e-123 | L | nUDIX hydrolase | |||
CNHFAHCC_02309 | 0.0 | psaA | C | PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX | ||
CNHFAHCC_02310 | 0.0 | psaB | C | PsaA and PsaB bind P700, the primary electron donor of photosystem I (PSI), as well as the electron acceptors A0, A1 and FX. PSI is a plastocyanin cytochrome c6-ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn. Oxidized P700 is reduced on the lumenal side of the thylakoid membrane by plastocyanin or cytochrome c6 | ||
CNHFAHCC_02311 | 6.9e-197 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
CNHFAHCC_02312 | 0.0 | V | ABC transporter transmembrane region | |||
CNHFAHCC_02313 | 9.7e-219 | icsA | M | Glycosyl transferases group 1 | ||
CNHFAHCC_02314 | 3.8e-224 | GT4 | M | Glycosyl transferases group 1 | ||
CNHFAHCC_02315 | 1.5e-255 | redA | S | Glycosyltransferase family 28 C-terminal domain | ||
CNHFAHCC_02316 | 7.5e-129 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_02317 | 1.5e-183 | pdhB | 1.2.4.1 | C | Transketolase, pyrimidine binding domain | |
CNHFAHCC_02318 | 1.5e-49 | ccmK3 | CQ | BMC | ||
CNHFAHCC_02319 | 2.2e-54 | ccmK4 | CQ | BMC domain | ||
CNHFAHCC_02320 | 1.3e-212 | glxK | 2.7.1.165 | G | Glycerate kinase family | |
CNHFAHCC_02321 | 0.0 | M | Carbohydrate-selective porin, OprB family | |||
CNHFAHCC_02322 | 1.8e-170 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
CNHFAHCC_02323 | 2.9e-303 | zwf | 1.1.1.363, 1.1.1.49 | F | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
CNHFAHCC_02324 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
CNHFAHCC_02325 | 1.7e-295 | |||||
CNHFAHCC_02326 | 4.7e-156 | L | Transposase | |||
CNHFAHCC_02327 | 3.3e-68 | S | PIN domain | |||
CNHFAHCC_02328 | 2.3e-66 | |||||
CNHFAHCC_02329 | 2.6e-13 | |||||
CNHFAHCC_02330 | 2.5e-205 | cobD | 4.1.1.81 | E | Aminotransferase class I and II | |
CNHFAHCC_02331 | 6.9e-47 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
CNHFAHCC_02332 | 5.9e-168 | 2.3.1.128, 2.3.1.59 | K | Acetyltransferase (GNAT) family | ||
CNHFAHCC_02333 | 8.8e-297 | G | Belongs to the glycosyl hydrolase 57 family | |||
CNHFAHCC_02334 | 2e-285 | recQ | 3.6.4.12 | L | RecQ zinc-binding | |
CNHFAHCC_02335 | 2.7e-160 | M | Glycosyltransferase like family 2 | |||
CNHFAHCC_02336 | 9.4e-206 | cbiD | 2.1.1.195 | H | Catalyzes the methylation of C-1 in cobalt-precorrin-5B to form cobalt-precorrin-6A | |
CNHFAHCC_02337 | 1.6e-182 | 4.2.1.46, 5.1.3.2 | GM | NAD(P)H-binding | ||
CNHFAHCC_02338 | 6e-77 | S | Protein of unknown function (DUF3782) | |||
CNHFAHCC_02339 | 1.3e-87 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
CNHFAHCC_02340 | 7.1e-235 | dinF | V | MatE | ||
CNHFAHCC_02341 | 1.8e-183 | crtR | I | Fatty acid desaturase | ||
CNHFAHCC_02342 | 6.8e-33 | S | Chlorophyll A-B binding protein | |||
CNHFAHCC_02343 | 2.7e-54 | |||||
CNHFAHCC_02344 | 4.1e-124 | sigG | K | ECF sigma factor | ||
CNHFAHCC_02345 | 1e-101 | 2.7.11.1 | K | transmembrane transcriptional regulator | ||
CNHFAHCC_02346 | 2e-180 | ycgR | S | Predicted permease | ||
CNHFAHCC_02348 | 2e-249 | pimA | M | Gkycosyl transferase family 4 group | ||
CNHFAHCC_02349 | 5e-34 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
CNHFAHCC_02350 | 3.4e-285 | S | Uncharacterized ACR, YdiU/UPF0061 family | |||
CNHFAHCC_02351 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
CNHFAHCC_02352 | 4.9e-193 | hypE | O | AIR synthase related protein, C-terminal domain | ||
CNHFAHCC_02353 | 9.6e-126 | S | Putative restriction endonuclease | |||
CNHFAHCC_02354 | 1e-135 | surE | 3.1.3.5 | S | Survival protein SurE | |
CNHFAHCC_02355 | 3.1e-101 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
CNHFAHCC_02356 | 6.8e-27 | |||||
CNHFAHCC_02357 | 1e-292 | lysS | 6.1.1.6 | J | tRNA synthetases class II (D, K and N) | |
CNHFAHCC_02358 | 8e-174 | rfbJ | M | Glycosyl transferase family 2 | ||
CNHFAHCC_02359 | 3e-162 | H | Methyltransferase FkbM domain | |||
CNHFAHCC_02360 | 0.0 | S | Psort location CytoplasmicMembrane, score | |||
CNHFAHCC_02361 | 2.2e-84 | S | Conserved nitrate reductase-associated protein (Nitr_red_assoc) | |||
CNHFAHCC_02362 | 5.6e-18 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_02363 | 0.0 | narB | 1.7.7.2, 1.8.1.2 | C | Molydopterin dinucleotide binding domain | |
CNHFAHCC_02365 | 2.5e-186 | nasD | 3.6.3.36 | P | ATPases associated with a variety of cellular activities | |
CNHFAHCC_02366 | 0.0 | nasD | 3.6.3.36 | P | NMT1/THI5 like | |
CNHFAHCC_02367 | 8e-146 | nrtB | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_02368 | 7.1e-250 | nrtA | P | NMT1-like family | ||
CNHFAHCC_02369 | 7.4e-205 | 2.4.2.18 | E | Glycosyl transferase family, a/b domain | ||
CNHFAHCC_02370 | 3.5e-125 | 3.1.3.3, 3.1.3.73, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
CNHFAHCC_02371 | 1.3e-51 | rlpA | M | Lytic transglycolase | ||
CNHFAHCC_02372 | 2.2e-235 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
CNHFAHCC_02373 | 5e-153 | ftsQ | 6.3.2.4 | M | POTRA domain, FtsQ-type | |
CNHFAHCC_02374 | 1.8e-234 | ctpA | 3.4.21.102 | M | tail specific protease | |
CNHFAHCC_02375 | 6.4e-130 | S | Putative restriction endonuclease | |||
CNHFAHCC_02376 | 2.7e-171 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
CNHFAHCC_02377 | 3.6e-82 | S | Domain of unknown function (DUF4168) | |||
CNHFAHCC_02378 | 1.7e-78 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
CNHFAHCC_02380 | 7.7e-161 | S | PRC-barrel domain | |||
CNHFAHCC_02381 | 4.1e-106 | |||||
CNHFAHCC_02383 | 0.0 | pcrA | 3.6.4.12 | L | UvrD-like helicase C-terminal domain | |
CNHFAHCC_02384 | 3e-90 | S | Bifunctional nuclease | |||
CNHFAHCC_02385 | 1.3e-173 | yfhF | S | Domain of unknown function (DUF1731) | ||
CNHFAHCC_02386 | 5.7e-233 | tupC | 3.6.3.55 | G | TOBE domain | |
CNHFAHCC_02387 | 1.2e-269 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_02388 | 9.4e-138 | pgmB | 3.1.3.18, 5.4.2.6 | S | Haloacid dehalogenase-like hydrolase | |
CNHFAHCC_02389 | 5.9e-140 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | SAICAR synthetase | |
CNHFAHCC_02390 | 0.0 | yaeT | M | POTRA domain, ShlB-type | ||
CNHFAHCC_02391 | 0.0 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
CNHFAHCC_02392 | 2.6e-272 | ybaR | P | Sulfate permease | ||
CNHFAHCC_02393 | 1.7e-151 | uspA | T | Universal stress protein | ||
CNHFAHCC_02394 | 5.1e-195 | S | Flavin containing amine oxidoreductase | |||
CNHFAHCC_02395 | 6.6e-101 | |||||
CNHFAHCC_02396 | 1.9e-42 | |||||
CNHFAHCC_02397 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Fumarate reductase flavoprotein C-term | |
CNHFAHCC_02398 | 2.8e-41 | bchB | S | Proto-chlorophyllide reductase 57 kD subunit | ||
CNHFAHCC_02399 | 1.4e-59 | hit | FG | HIT domain | ||
CNHFAHCC_02400 | 4.8e-173 | acoC | 2.3.1.12 | I | Serine aminopeptidase, S33 | |
CNHFAHCC_02401 | 7e-95 | S | Uncharacterized ACR, COG1430 | |||
CNHFAHCC_02402 | 4.3e-25 | bfd | P | BFD-like [2Fe-2S] binding domain | ||
CNHFAHCC_02403 | 2.2e-284 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
CNHFAHCC_02404 | 1.3e-78 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
CNHFAHCC_02405 | 9e-272 | codA | 3.5.4.1 | F | Amidohydrolase family | |
CNHFAHCC_02406 | 6.3e-60 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
CNHFAHCC_02407 | 1.7e-41 | |||||
CNHFAHCC_02408 | 1.8e-172 | todF | I | Serine aminopeptidase, S33 | ||
CNHFAHCC_02409 | 3e-33 | |||||
CNHFAHCC_02410 | 6.7e-46 | grxC | O | Glutaredoxin | ||
CNHFAHCC_02411 | 1.6e-182 | gshB | 6.3.2.2, 6.3.2.3 | F | Prokaryotic glutathione synthetase, N-terminal domain | |
CNHFAHCC_02412 | 1.1e-43 | |||||
CNHFAHCC_02413 | 2e-160 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
CNHFAHCC_02414 | 2.4e-271 | pntA | 1.6.1.2 | C | Alanine dehydrogenase/PNT, C-terminal domain | |
CNHFAHCC_02415 | 3.5e-94 | |||||
CNHFAHCC_02416 | 1e-57 | S | Nucleotidyltransferase domain | |||
CNHFAHCC_02417 | 1.6e-24 | N | HicA toxin of bacterial toxin-antitoxin, | |||
CNHFAHCC_02418 | 1.1e-36 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_02419 | 9.6e-256 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
CNHFAHCC_02420 | 1.4e-245 | pmbA | S | Putative modulator of DNA gyrase | ||
CNHFAHCC_02421 | 1.3e-162 | 2.1.1.79 | M | Methyltransferase domain | ||
CNHFAHCC_02422 | 4.7e-60 | 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | ||
CNHFAHCC_02423 | 8.6e-175 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
CNHFAHCC_02424 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
CNHFAHCC_02425 | 1.4e-31 | |||||
CNHFAHCC_02426 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunits gamma and tau domain III | |
CNHFAHCC_02427 | 1.6e-81 | S | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
CNHFAHCC_02428 | 0.0 | tsdA | 1.8.2.2 | C | Cytochrome C oxidase, cbb3-type, subunit III | |
CNHFAHCC_02429 | 1.1e-233 | oxdD | 4.1.1.2 | G | Cupin | |
CNHFAHCC_02430 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
CNHFAHCC_02432 | 6.5e-65 | S | ATPase (AAA superfamily | |||
CNHFAHCC_02433 | 4e-98 | S | Putative restriction endonuclease | |||
CNHFAHCC_02434 | 1.8e-08 | S | Protein of unknown function (DUF2442) | |||
CNHFAHCC_02435 | 5.1e-164 | nqrB | 1.6.5.8 | U | NQR2, RnfD, RnfE family | |
CNHFAHCC_02436 | 0.0 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_02437 | 5e-195 | S | CHAD | |||
CNHFAHCC_02440 | 0.0 | recJ | L | DHH family | ||
CNHFAHCC_02441 | 0.0 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_02442 | 1.8e-270 | 2.7.13.3 | S | Predicted membrane protein (DUF2079) | ||
CNHFAHCC_02443 | 3e-178 | cscK | 2.7.1.4 | G | pfkB family carbohydrate kinase | |
CNHFAHCC_02444 | 2.6e-85 | cybB | C | Prokaryotic cytochrome b561 | ||
CNHFAHCC_02445 | 2.4e-50 | |||||
CNHFAHCC_02446 | 1.2e-208 | 2.1.1.63 | S | Pentapeptide repeats (8 copies) | ||
CNHFAHCC_02447 | 6.4e-122 | cbbZp | 1.17.99.6, 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
CNHFAHCC_02448 | 1.1e-172 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
CNHFAHCC_02449 | 3.7e-90 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
CNHFAHCC_02450 | 3.3e-23 | psbZ | U | Controls the interaction of photosystem II (PSII) cores with the light-harvesting antenna | ||
CNHFAHCC_02452 | 6.5e-179 | rps1a | J | Ribosomal protein S1-like RNA-binding domain | ||
CNHFAHCC_02453 | 1.3e-156 | L | Transposase | |||
CNHFAHCC_02454 | 2.3e-215 | recF | F | linear DNA. It also seems to bind ATP | ||
CNHFAHCC_02455 | 5.6e-289 | mdlB | V | ABC transporter transmembrane region | ||
CNHFAHCC_02456 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | F | Pyruvate kinase, barrel domain | |
CNHFAHCC_02457 | 4.8e-72 | S | Domain of unknown function (DUF1824) | |||
CNHFAHCC_02458 | 1.4e-103 | S | Protein of unknown function (DUF2396) | |||
CNHFAHCC_02459 | 7.1e-294 | pap | S | Polyphosphate kinase 2 (PPK2) | ||
CNHFAHCC_02460 | 4.3e-200 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
CNHFAHCC_02461 | 6.6e-119 | bioY | S | BioY family | ||
CNHFAHCC_02462 | 2.9e-87 | lspA | 3.4.23.36 | MU | Signal peptidase (SPase) II | |
CNHFAHCC_02463 | 8e-271 | 2.7.1.74, 2.7.1.76 | F | nucleoside 2-deoxyribosyltransferase | ||
CNHFAHCC_02464 | 3.9e-139 | S | Domain of unknown function (DUF4393) | |||
CNHFAHCC_02465 | 2.7e-25 | |||||
CNHFAHCC_02466 | 0.0 | M | Carbohydrate-selective porin, OprB family | |||
CNHFAHCC_02467 | 1.7e-293 | glnH | P | Bacterial periplasmic substrate-binding proteins | ||
CNHFAHCC_02468 | 5.4e-43 | |||||
CNHFAHCC_02469 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
CNHFAHCC_02470 | 4.7e-128 | cbiT | 2.1.1.132, 2.1.1.196 | H | Putative methyltransferase | |
CNHFAHCC_02471 | 6.2e-165 | cdsA | 2.7.7.41 | I | Cytidylyltransferase family | |
CNHFAHCC_02472 | 1.3e-287 | NU | Pilus assembly protein PilX | |||
CNHFAHCC_02473 | 1.1e-77 | |||||
CNHFAHCC_02474 | 0.0 | S | TamB, inner membrane protein subunit of TAM complex | |||
CNHFAHCC_02475 | 2.6e-271 | K | AAA-like domain | |||
CNHFAHCC_02476 | 3.4e-63 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
CNHFAHCC_02477 | 6.2e-114 | ruvA | 3.6.4.12 | F | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
CNHFAHCC_02478 | 4e-139 | S | Integral membrane protein DUF92 | |||
CNHFAHCC_02479 | 1.3e-248 | fccB | 1.8.5.4 | S | Pyridine nucleotide-disulphide oxidoreductase | |
CNHFAHCC_02480 | 8.9e-40 | rbpD | S | RNA recognition motif | ||
CNHFAHCC_02481 | 2.1e-271 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
CNHFAHCC_02482 | 1.4e-141 | nlpD | 3.4.24.75 | M | Peptidase family M23 | |
CNHFAHCC_02483 | 1.1e-68 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
CNHFAHCC_02484 | 0.0 | yloA | K | Domain of unknown function (DUF814) | ||
CNHFAHCC_02485 | 8e-229 | nspC | 4.1.1.96 | E | Pyridoxal-dependent decarboxylase, C-terminal sheet domain | |
CNHFAHCC_02486 | 5.8e-32 | hemH | 4.99.1.1, 4.99.1.9 | H | PFAM Chlorophyll A-B binding protein | |
CNHFAHCC_02487 | 1.9e-52 | |||||
CNHFAHCC_02488 | 7.1e-60 | |||||
CNHFAHCC_02489 | 1.6e-216 | lptG | S | Predicted permease YjgP/YjgQ family | ||
CNHFAHCC_02491 | 6.4e-276 | psr | K | LytR cell envelope-related transcriptional attenuator | ||
CNHFAHCC_02492 | 1.3e-75 | |||||
CNHFAHCC_02493 | 2.2e-193 | gapA | 1.2.1.12, 1.2.1.59 | F | Glyceraldehyde 3-phosphate dehydrogenase, C-terminal domain | |
CNHFAHCC_02495 | 7.1e-109 | S | COGs COG4636 conserved | |||
CNHFAHCC_02496 | 1.1e-112 | aat | 2.3.2.6 | O | Functions in the N-end rule pathway of protein degradation where it conjugates Leu, Phe and, less efficiently, Met from aminoacyl-tRNAs to the N-termini of proteins containing an N-terminal arginine or lysine | |
CNHFAHCC_02497 | 2.3e-175 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
CNHFAHCC_02498 | 2.5e-241 | S | Aldo/keto reductase family | |||
CNHFAHCC_02499 | 6.3e-126 | IQ | KR domain | |||
CNHFAHCC_02500 | 4e-166 | ilvE | 2.6.1.42, 4.1.3.38 | EH | Amino-transferase class IV | |
CNHFAHCC_02501 | 3.3e-86 | |||||
CNHFAHCC_02502 | 7.5e-233 | S | ABC1 family | |||
CNHFAHCC_02503 | 1.6e-39 | S | unusual protein kinase | |||
CNHFAHCC_02504 | 8.7e-66 | S | Aspartyl protease | |||
CNHFAHCC_02505 | 0.0 | uvrC | J | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
CNHFAHCC_02506 | 0.0 | amiA | 2.7.11.1, 3.4.21.107, 3.5.1.28 | M | Bacterial SH3 domain homologues | |
CNHFAHCC_02507 | 4.6e-92 | S | JAB/MPN domain | |||
CNHFAHCC_02508 | 1.5e-70 | |||||
CNHFAHCC_02509 | 2.3e-276 | S | Peptidase family M50 | |||
CNHFAHCC_02510 | 8.8e-162 | murQ | 4.2.1.126 | S | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
CNHFAHCC_02511 | 2.6e-94 | S | Protein of unknown function (DUF3110) | |||
CNHFAHCC_02512 | 1.7e-182 | petA | 1.8.2.2 | C | Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions | |
CNHFAHCC_02513 | 2.7e-102 | petC | 1.10.9.1 | C | Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions | |
CNHFAHCC_02514 | 2.1e-28 | psbH | S | Photosystem II 10 kDa phosphoprotein | ||
CNHFAHCC_02515 | 1.5e-14 | psbN | S | May play a role in photosystem I and II biogenesis | ||
CNHFAHCC_02516 | 2.1e-47 | S | YCII-related domain | |||
CNHFAHCC_02517 | 3e-198 | S | WD40 repeats | |||
CNHFAHCC_02518 | 3.2e-206 | dctP | G | Bacterial extracellular solute-binding protein, family 7 | ||
CNHFAHCC_02519 | 0.0 | Q | FG-GAP repeat | |||
CNHFAHCC_02520 | 3.9e-128 | IQ | KR domain | |||
CNHFAHCC_02521 | 1.6e-94 | S | Haem-degrading | |||
CNHFAHCC_02522 | 4.7e-157 | G | Cupin 2, conserved barrel domain protein | |||
CNHFAHCC_02523 | 5.4e-101 | S | WD40 repeats | |||
CNHFAHCC_02524 | 3.5e-148 | S | WD40 repeats | |||
CNHFAHCC_02525 | 3.3e-89 | hbpS | S | Haem-degrading | ||
CNHFAHCC_02526 | 1.2e-196 | G | Polysaccharide deacetylase | |||
CNHFAHCC_02527 | 5.1e-175 | S | alpha/beta hydrolase fold | |||
CNHFAHCC_02528 | 1.5e-171 | 5.1.3.30, 5.1.3.31 | G | Xylose isomerase-like TIM barrel | ||
CNHFAHCC_02529 | 9.8e-157 | G | Oxalate decarboxylase | |||
CNHFAHCC_02530 | 9.3e-25 | |||||
CNHFAHCC_02531 | 1.2e-154 | G | Cupin 2, conserved barrel domain protein | |||
CNHFAHCC_02532 | 1.2e-76 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
CNHFAHCC_02533 | 1.1e-111 | |||||
CNHFAHCC_02534 | 2.6e-58 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
CNHFAHCC_02535 | 2.9e-113 | 3.5.1.124 | S | DJ-1/PfpI family | ||
CNHFAHCC_02536 | 0.0 | 5.1.3.11, 5.1.3.8 | G | PFAM N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | ||
CNHFAHCC_02537 | 3e-51 | T | STAS domain | |||
CNHFAHCC_02538 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Carbohydrate-binding module 48 (Isoamylase N-terminal domain) |
CNHFAHCC_02539 | 1.3e-51 | T | STAS domain | |||
CNHFAHCC_02540 | 0.0 | sigB | 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
CNHFAHCC_02541 | 9.1e-77 | btrW | 2.7.11.1, 3.1.3.3 | T | Histidine kinase-like ATPase domain | |
CNHFAHCC_02542 | 4e-130 | L | transposition | |||
CNHFAHCC_02543 | 8.4e-190 | L | PFAM Transposase | |||
CNHFAHCC_02544 | 1.9e-294 | |||||
CNHFAHCC_02545 | 9.2e-195 | S | Membrane transport protein | |||
CNHFAHCC_02546 | 6e-247 | MA20_03685 | G | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_02547 | 1.6e-108 | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | ||
CNHFAHCC_02548 | 3.9e-190 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
CNHFAHCC_02549 | 2.3e-119 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
CNHFAHCC_02550 | 0.0 | 3.2.1.45 | GH116 | G | beta-glucosidase 2, glycosyl-hydrolase family 116 N-term | |
CNHFAHCC_02551 | 3.4e-14 | S | Uncharacterised protein family (UPF0175) | |||
CNHFAHCC_02552 | 5.6e-125 | S | transposase or invertase | |||
CNHFAHCC_02553 | 9.1e-133 | |||||
CNHFAHCC_02555 | 1.5e-135 | S | NYN domain | |||
CNHFAHCC_02556 | 4.2e-23 | S | PFAM Iron-binding zinc finger CDGSH type | |||
CNHFAHCC_02557 | 1.6e-134 | yhhW | S | Pirin | ||
CNHFAHCC_02558 | 8.5e-162 | MA20_14610 | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
CNHFAHCC_02559 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
CNHFAHCC_02560 | 9.8e-143 | prpC | 3.1.3.16 | T | Serine/threonine phosphatases, family 2C, catalytic domain | |
CNHFAHCC_02561 | 0.0 | S | ABC1 family | |||
CNHFAHCC_02562 | 4.2e-07 | |||||
CNHFAHCC_02563 | 2.3e-48 | S | granule-associated protein | |||
CNHFAHCC_02564 | 2.2e-44 | |||||
CNHFAHCC_02565 | 5.3e-23 | |||||
CNHFAHCC_02566 | 1.9e-175 | oppB | U | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_02567 | 8.5e-209 | ddl | 6.3.2.4 | F | D-ala D-ala ligase N-terminus | |
CNHFAHCC_02568 | 5.8e-112 | exoD | S | Exopolysaccharide synthesis, ExoD | ||
CNHFAHCC_02569 | 1.3e-50 | clpS | S | ATP-dependent Clp protease adaptor protein ClpS | ||
CNHFAHCC_02570 | 5e-84 | hoxW | C | TIGRFAM hydrogenase maturation protease | ||
CNHFAHCC_02571 | 3.8e-54 | rpsF | 4.3.1.19 | J | Binds together with S18 to 16S ribosomal RNA | |
CNHFAHCC_02572 | 3.2e-155 | hpcE | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
CNHFAHCC_02573 | 3.7e-135 | cpcE | 4.4.1.32 | C | PBS lyase HEAT-like repeat | |
CNHFAHCC_02574 | 1.1e-241 | aslB | C | Radical SAM superfamily | ||
CNHFAHCC_02575 | 4e-87 | |||||
CNHFAHCC_02576 | 7.1e-37 | |||||
CNHFAHCC_02577 | 1.1e-42 | |||||
CNHFAHCC_02578 | 8.3e-165 | ET | Bacterial periplasmic substrate-binding proteins | |||
CNHFAHCC_02579 | 7.3e-135 | cobI | 2.1.1.130, 2.1.1.131, 2.1.1.151 | H | Tetrapyrrole (Corrin/Porphyrin) Methylases | |
CNHFAHCC_02580 | 9.3e-112 | O | Bacterial protein of unknown function (DUF922) | |||
CNHFAHCC_02581 | 3.2e-172 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
CNHFAHCC_02582 | 1.5e-224 | mdsC | 2.7.1.162, 2.7.1.39 | S | Phosphotransferase enzyme family | |
CNHFAHCC_02583 | 2.3e-281 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
CNHFAHCC_02584 | 4.3e-41 | C | 4Fe-4S binding domain | |||
CNHFAHCC_02585 | 7e-130 | livF | E | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_02586 | 4.9e-160 | ribF | 2.7.1.26, 2.7.7.2 | F | Riboflavin kinase | |
CNHFAHCC_02587 | 1.4e-126 | M | protein involved in exopolysaccharide biosynthesis | |||
CNHFAHCC_02588 | 1.5e-48 | S | Protein of unknown function (DUF3143) | |||
CNHFAHCC_02589 | 8.5e-34 | cp12 | S | CP12 | ||
CNHFAHCC_02590 | 7.4e-194 | trpS | 6.1.1.2 | J | tRNA synthetases class I (W and Y) | |
CNHFAHCC_02591 | 4.9e-18 | |||||
CNHFAHCC_02592 | 1.5e-106 | nadD | 2.7.6.3, 2.7.7.18 | H | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
CNHFAHCC_02593 | 2.4e-83 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
CNHFAHCC_02594 | 1e-215 | |||||
CNHFAHCC_02595 | 7.8e-177 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
CNHFAHCC_02596 | 0.0 | CJ | Acetyl-CoA hydrolase/transferase C-terminal domain | |||
CNHFAHCC_02597 | 0.0 | pta | 2.3.1.8 | F | Involved in acetate metabolism | |
CNHFAHCC_02598 | 6.5e-76 | V | (ABC) transporter | |||
CNHFAHCC_02599 | 1.3e-136 | sfsA | S | Sugar fermentation stimulation protein | ||
CNHFAHCC_02600 | 5.7e-106 | S | Protein of unknown function (DUF1997) | |||
CNHFAHCC_02601 | 5.9e-169 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_02602 | 2.7e-122 | queE | 1.97.1.4, 4.3.99.3 | F | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
CNHFAHCC_02603 | 1.8e-267 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
CNHFAHCC_02604 | 4.6e-249 | ymfH | S | Peptidase M16 inactive domain | ||
CNHFAHCC_02605 | 4.1e-250 | S | Peptidase M16 inactive domain | |||
CNHFAHCC_02606 | 9.1e-144 | hupE | O | HupE / UreJ protein | ||
CNHFAHCC_02607 | 3.4e-230 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
CNHFAHCC_02608 | 1.3e-72 | V | HNH nucleases | |||
CNHFAHCC_02609 | 5.1e-57 | |||||
CNHFAHCC_02610 | 0.0 | gyrB | 3.6.4.12, 4.2.1.46, 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
CNHFAHCC_02611 | 2.3e-43 | S | Protein CHLORORESPIRATORY REDUCTION 7 | |||
CNHFAHCC_02612 | 3.7e-12 | psbY | U | Manganese-binding polypeptide with L-arginine metabolizing enzyme activity. Component of the core of photosystem II | ||
CNHFAHCC_02613 | 7.2e-189 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
CNHFAHCC_02614 | 4.6e-264 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
CNHFAHCC_02615 | 4e-239 | cefD | E | Aminotransferase class-V | ||
CNHFAHCC_02616 | 4.5e-171 | S | Protein of unknown function (DUF1092) | |||
CNHFAHCC_02617 | 3.9e-153 | |||||
CNHFAHCC_02618 | 1.2e-177 | dam | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
CNHFAHCC_02619 | 6.2e-156 | L | Transposase | |||
CNHFAHCC_02620 | 3.6e-137 | IQ | KR domain | |||
CNHFAHCC_02621 | 6.1e-53 | S | Domain of unknown function (DUF427) | |||
CNHFAHCC_02622 | 8.1e-120 | K | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_02623 | 0.0 | T | MASE1 | |||
CNHFAHCC_02624 | 3e-147 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_02625 | 0.0 | sppA | OU | Peptidase family S49 | ||
CNHFAHCC_02626 | 1e-87 | ycf51 | S | Protein of function (DUF2518) | ||
CNHFAHCC_02627 | 3.6e-148 | I | Serine aminopeptidase, S33 | |||
CNHFAHCC_02628 | 1.6e-230 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
CNHFAHCC_02629 | 3.2e-144 | |||||
CNHFAHCC_02630 | 0.0 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
CNHFAHCC_02631 | 2.2e-66 | |||||
CNHFAHCC_02632 | 5e-184 | S | Domain of unknown function (DUF362) | |||
CNHFAHCC_02633 | 7e-83 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02634 | 4.5e-85 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02635 | 4.1e-83 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02636 | 1.4e-83 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02637 | 1.1e-100 | S | Methyltransferase domain | |||
CNHFAHCC_02638 | 0.0 | O | Glycosyl transferase family 41 | |||
CNHFAHCC_02639 | 2.8e-151 | S | Tetratricopeptide repeat | |||
CNHFAHCC_02640 | 4.7e-88 | NU | general secretion pathway protein | |||
CNHFAHCC_02641 | 5.7e-86 | U | Type IV pilin-like G and H, putative | |||
CNHFAHCC_02642 | 7e-261 | Q | Protein of unknown function (DUF1698) | |||
CNHFAHCC_02643 | 1e-86 | S | ATPase (AAA superfamily | |||
CNHFAHCC_02644 | 1.9e-77 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_02645 | 6.2e-60 | S | Domain of unknown function (DUF4351) | |||
CNHFAHCC_02646 | 4.9e-09 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_02647 | 4.9e-199 | sigE | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_02648 | 6e-249 | thrC1 | 4.2.3.1 | E | Pyridoxal-phosphate dependent enzyme | |
CNHFAHCC_02649 | 5.5e-283 | arnT_1 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
CNHFAHCC_02650 | 0.0 | T | diguanylate cyclase | |||
CNHFAHCC_02651 | 1.3e-180 | rseP | M | Peptidase family M50 | ||
CNHFAHCC_02652 | 2.7e-120 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
CNHFAHCC_02653 | 5.4e-80 | |||||
CNHFAHCC_02654 | 2.8e-90 | tadA | 3.4.17.13, 3.5.4.1, 3.5.4.3, 3.5.4.33, 3.8.1.5 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
CNHFAHCC_02655 | 4.1e-69 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02656 | 6.7e-281 | phrB | 4.1.99.3 | K | DNA photolyase | |
CNHFAHCC_02657 | 6.9e-172 | S | Tetratricopeptide repeats | |||
CNHFAHCC_02658 | 2.9e-262 | opcA | GM | Putative peptidoglycan binding domain | ||
CNHFAHCC_02659 | 3e-139 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
CNHFAHCC_02660 | 2.6e-109 | lexA | 3.4.21.88 | K | LexA DNA binding domain | |
CNHFAHCC_02661 | 8.8e-192 | sdhB | 1.3.5.1, 1.3.5.4 | C | 2Fe-2S iron-sulfur cluster binding domain | |
CNHFAHCC_02662 | 7.8e-188 | MA20_23615 | T | HD domain | ||
CNHFAHCC_02663 | 8.5e-122 | bioM | 3.6.3.55 | P | ATPases associated with a variety of cellular activities | |
CNHFAHCC_02664 | 6.5e-173 | 2.5.1.115, 2.5.1.116 | H | UbiA prenyltransferase family | ||
CNHFAHCC_02665 | 1.5e-229 | 5.5.1.24 | S | Tocopherol cyclase | ||
CNHFAHCC_02666 | 1.4e-109 | O | Redoxin | |||
CNHFAHCC_02667 | 2.6e-76 | perR | P | Ferric uptake regulator family | ||
CNHFAHCC_02668 | 5e-84 | S | Protein of unknown function (DUF1499) | |||
CNHFAHCC_02669 | 7.6e-64 | psb28-2 | S | Psb28 protein | ||
CNHFAHCC_02670 | 0.0 | appA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
CNHFAHCC_02672 | 3e-102 | S | Alternative locus ID | |||
CNHFAHCC_02673 | 1.6e-148 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
CNHFAHCC_02674 | 1.9e-233 | ndbB | 1.6.99.3 | C | Pyridine nucleotide-disulphide oxidoreductase | |
CNHFAHCC_02675 | 0.0 | amiC | 3.5.1.28 | M | Ami_3 | |
CNHFAHCC_02676 | 1.9e-158 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
CNHFAHCC_02677 | 1.1e-269 | P | Pheophorbide a oxygenase | |||
CNHFAHCC_02678 | 2.1e-257 | ndh | 1.6.99.3 | C | Pyridine nucleotide-disulphide oxidoreductase | |
CNHFAHCC_02679 | 2.7e-73 | |||||
CNHFAHCC_02680 | 4.4e-88 | rimI | 2.3.1.128 | K | FR47-like protein | |
CNHFAHCC_02681 | 6.7e-297 | phr | 4.1.99.3 | L | DNA photolyase | |
CNHFAHCC_02682 | 4.1e-84 | NPTU | Heavy-metal resistance | |||
CNHFAHCC_02683 | 3.9e-68 | |||||
CNHFAHCC_02684 | 1.2e-101 | sigH | K | ECF sigma factor | ||
CNHFAHCC_02685 | 2.1e-252 | clcA | P | Voltage gated chloride channel | ||
CNHFAHCC_02686 | 3e-178 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
CNHFAHCC_02687 | 1.9e-100 | J | Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins | |||
CNHFAHCC_02688 | 5.9e-28 | |||||
CNHFAHCC_02689 | 2.2e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_02690 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_02691 | 1.5e-277 | psbC | A | One of the components of the core complex of photosystem II (PSII). It binds chlorophyll and helps catalyze the primary light-induced photochemical processes of PSII. PSII is a light- driven water plastoquinone oxidoreductase, using light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation | ||
CNHFAHCC_02692 | 5e-209 | psbD | 1.10.3.9 | C | Photosystem II (PSII) is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1 D2 (PsbA PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors. D2 is needed for assembly of a stable PSII complex | |
CNHFAHCC_02693 | 4.6e-252 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
CNHFAHCC_02694 | 1.8e-66 | S | Domain of unknown function (DUF202) | |||
CNHFAHCC_02695 | 2.6e-214 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
CNHFAHCC_02696 | 4.7e-51 | S | Protein of unknown function (DUF1232) | |||
CNHFAHCC_02697 | 5.5e-186 | lmbP | 2.7.1.168 | S | GHMP kinases C terminal | |
CNHFAHCC_02698 | 2.9e-273 | S | Putative modulator of DNA gyrase | |||
CNHFAHCC_02699 | 1.5e-208 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
CNHFAHCC_02700 | 2.3e-217 | |||||
CNHFAHCC_02701 | 5.3e-302 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha-amylase domain |
CNHFAHCC_02702 | 9.6e-311 | S | ABC transporter | |||
CNHFAHCC_02703 | 6.2e-193 | egtD | 2.1.1.44 | S | Histidine-specific methyltransferase, SAM-dependent | |
CNHFAHCC_02704 | 1.9e-109 | |||||
CNHFAHCC_02705 | 5.3e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
CNHFAHCC_02706 | 2.1e-59 | S | Tetratricopeptide repeat | |||
CNHFAHCC_02707 | 1.2e-88 | |||||
CNHFAHCC_02708 | 1.6e-49 | KLT | Protein tyrosine kinase | |||
CNHFAHCC_02709 | 0.0 | S | Dynamin family | |||
CNHFAHCC_02710 | 3.5e-61 | S | KGK domain | |||
CNHFAHCC_02712 | 3.1e-15 | S | KGK domain | |||
CNHFAHCC_02713 | 2.6e-200 | lptC | S | Lipopolysaccharide-assembly, LptC-related | ||
CNHFAHCC_02714 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
CNHFAHCC_02715 | 0.0 | |||||
CNHFAHCC_02716 | 1.5e-186 | 3.1.3.16 | U | EamA-like transporter family | ||
CNHFAHCC_02717 | 1.5e-61 | S | Cupin domain | |||
CNHFAHCC_02718 | 8.1e-131 | S | Protein of unknown function (DUF4079) | |||
CNHFAHCC_02719 | 3.1e-184 | 4.6.1.1 | CT | PFAM Adenylate and Guanylate cyclase catalytic domain | ||
CNHFAHCC_02720 | 4.7e-82 | |||||
CNHFAHCC_02721 | 8.3e-122 | O | Redoxin | |||
CNHFAHCC_02722 | 7.3e-62 | |||||
CNHFAHCC_02723 | 9.6e-169 | K | LysR substrate binding domain | |||
CNHFAHCC_02724 | 4.3e-45 | L | Transposase | |||
CNHFAHCC_02725 | 3.4e-97 | L | PFAM transposase, IS4 family protein | |||
CNHFAHCC_02726 | 8.4e-47 | L | PFAM IS1 transposase | |||
CNHFAHCC_02727 | 2.1e-52 | S | Protein of unknown function (DUF2973) | |||
CNHFAHCC_02728 | 4.4e-214 | norA | EGP | MFS_1 like family | ||
CNHFAHCC_02729 | 3.6e-185 | P | PBP superfamily domain | |||
CNHFAHCC_02730 | 1e-171 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
CNHFAHCC_02731 | 2.1e-149 | pstA | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_02732 | 4.4e-149 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
CNHFAHCC_02733 | 8e-96 | 5.2.1.8 | J | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | ||
CNHFAHCC_02734 | 1.1e-49 | phhB | 4.2.1.96 | H | Pterin 4 alpha carbinolamine dehydratase | |
CNHFAHCC_02735 | 0.0 | S | Domain of unknown function (DUF389) | |||
CNHFAHCC_02736 | 1.6e-41 | T | Domain of unknown function (DUF1816) | |||
CNHFAHCC_02737 | 3.5e-102 | S | Inhibitor of apoptosis-promoting Bax1 | |||
CNHFAHCC_02738 | 1.5e-43 | |||||
CNHFAHCC_02739 | 4.5e-282 | pds | 1.17.8.1, 1.3.5.5, 1.3.5.6 | CH | Flavin containing amine oxidoreductase | |
CNHFAHCC_02740 | 2.9e-198 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.96, 2.5.1.99 | I | Squalene/phytoene synthase | |
CNHFAHCC_02741 | 6.7e-69 | 2.5.1.18 | S | MAPEG family | ||
CNHFAHCC_02742 | 1.4e-47 | ureA | 3.5.1.5 | E | Urease, gamma subunit | |
CNHFAHCC_02744 | 9.8e-222 | ET | Ligand-gated ion channel | |||
CNHFAHCC_02745 | 3.8e-126 | S | periplasmic protein | |||
CNHFAHCC_02746 | 5.9e-134 | S | Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid | |||
CNHFAHCC_02747 | 4e-98 | S | Protein of unknown function (DUF3122) | |||
CNHFAHCC_02748 | 1.1e-92 | ygaP | P | Rhodanese Homology Domain | ||
CNHFAHCC_02749 | 1.1e-150 | S | Sulfite exporter TauE/SafE | |||
CNHFAHCC_02750 | 3.2e-272 | flgE | N | Protein of unknown function (DUF3370) | ||
CNHFAHCC_02751 | 2e-211 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
CNHFAHCC_02752 | 6.6e-72 | |||||
CNHFAHCC_02753 | 8e-151 | 3.1.3.15, 3.1.3.25, 3.1.3.93 | G | Inositol monophosphatase family | ||
CNHFAHCC_02754 | 2.1e-199 | hisC | 2.6.1.9 | E | Aminotransferase class I and II | |
CNHFAHCC_02755 | 1.2e-54 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
CNHFAHCC_02756 | 2.3e-136 | aqpZ | U | Channel that permits osmotically driven movement of water in both directions. It is involved in the osmoregulation and in the maintenance of cell turgor during volume expansion in rapidly growing cells. It mediates rapid entry or exit of water in response to abrupt changes in osmolarity | ||
CNHFAHCC_02757 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
CNHFAHCC_02758 | 6.4e-56 | CP | 4Fe-4S dicluster domain | |||
CNHFAHCC_02759 | 3.5e-271 | I | Phosphate acyltransferases | |||
CNHFAHCC_02760 | 1.6e-16 | |||||
CNHFAHCC_02761 | 1.1e-106 | S | Putative restriction endonuclease | |||
CNHFAHCC_02762 | 5.2e-62 | |||||
CNHFAHCC_02763 | 9.1e-52 | S | Protein of unknown function (DUF2442) | |||
CNHFAHCC_02764 | 2.6e-222 | L | Probable transposase | |||
CNHFAHCC_02765 | 0.0 | Q | calcium- and calmodulin-responsive adenylate cyclase activity | |||
CNHFAHCC_02766 | 1.2e-134 | H | Methyltransferase FkbM domain | |||
CNHFAHCC_02767 | 1.4e-122 | |||||
CNHFAHCC_02768 | 7.3e-83 | apcA | O | Light-harvesting photosynthetic bile pigment-protein from the phycobiliprotein complex. Allophycocyanin has a maximum absorption at approximately 650 nanometers | ||
CNHFAHCC_02769 | 2.4e-81 | apcB | O | Light-harvesting photosynthetic bile pigment-protein from the phycobiliprotein complex. Allophycocyanin has a maximum absorption at approximately 650 nanometers | ||
CNHFAHCC_02770 | 6.1e-31 | apcC | O | Rod linker protein, associated with allophycocyanin. Linker polypeptides determine the state of aggregation and the location of the disk-shaped phycobiliprotein units within the phycobilisome and modulate their spectroscopic properties in order to mediate a directed and optimal energy transfer (By similarity) | ||
CNHFAHCC_02771 | 2.7e-179 | prmA | J | Ribosomal protein L11 methyltransferase (PrmA) | ||
CNHFAHCC_02772 | 8.5e-290 | serA | 1.1.1.310, 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
CNHFAHCC_02773 | 6.5e-136 | S | Protein of unknown function (DUF3120) | |||
CNHFAHCC_02774 | 2.1e-196 | cyaA | 4.6.1.1 | T | Adenylyl- / guanylyl cyclase, catalytic domain | |
CNHFAHCC_02775 | 1.3e-84 | btuE | 1.11.1.22, 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
CNHFAHCC_02776 | 1.8e-230 | phaA | 2.3.1.9 | I | Thiolase, C-terminal domain | |
CNHFAHCC_02777 | 1e-128 | IQ | KR domain | |||
CNHFAHCC_02778 | 4.8e-263 | pucC | G | PUCC protein | ||
CNHFAHCC_02779 | 0.0 | letS | 2.7.13.3 | T | Histidine Phosphotransfer domain | |
CNHFAHCC_02780 | 4.5e-249 | C | FAD dependent oxidoreductase | |||
CNHFAHCC_02781 | 2.7e-70 | N | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_02782 | 9.6e-159 | S | S-layer homology domain | |||
CNHFAHCC_02783 | 1e-153 | cphB | 3.4.15.6 | PQ | Exopeptidase that catalyzes the hydrolytic cleavage of multi-L-arginyl-poly-L-aspartic acid (cyanophycin | |
CNHFAHCC_02784 | 0.0 | cphA | 6.3.2.13, 6.3.2.29, 6.3.2.30 | HJM | RimK-like ATP-grasp domain | |
CNHFAHCC_02785 | 8.5e-124 | S | Domain of unknown function (DUF4129) | |||
CNHFAHCC_02786 | 2.5e-241 | 2.5.1.18 | O | Glutathione S-transferase, C-terminal domain | ||
CNHFAHCC_02787 | 2.1e-48 | |||||
CNHFAHCC_02788 | 1.8e-283 | S | amine dehydrogenase activity | |||
CNHFAHCC_02789 | 4.4e-13 | S | HicB family | |||
CNHFAHCC_02790 | 1.3e-124 | S | transposase or invertase | |||
CNHFAHCC_02791 | 1.5e-250 | mnmE | J | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
CNHFAHCC_02792 | 0.0 | ctpF | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
CNHFAHCC_02793 | 1e-79 | |||||
CNHFAHCC_02794 | 8.6e-256 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
CNHFAHCC_02795 | 1.3e-220 | I | Fatty acid desaturase | |||
CNHFAHCC_02796 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_02797 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_02798 | 4.5e-94 | S | Putative restriction endonuclease | |||
CNHFAHCC_02799 | 0.0 | E | Domain of unknown function (DUF3488) | |||
CNHFAHCC_02801 | 1.2e-149 | S | NAD synthase | |||
CNHFAHCC_02802 | 2.5e-141 | S | DUF218 domain | |||
CNHFAHCC_02803 | 1.6e-88 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
CNHFAHCC_02804 | 5.7e-132 | comB | 3.1.3.71 | H | 2-phosphosulpholactate phosphatase | |
CNHFAHCC_02805 | 4.2e-112 | ydgI | C | Nitroreductase family | ||
CNHFAHCC_02806 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
CNHFAHCC_02807 | 6.8e-289 | U | Involved in the tonB-independent uptake of proteins | |||
CNHFAHCC_02808 | 3.6e-213 | guaB3 | 1.1.1.205 | F | IMP dehydrogenase / GMP reductase domain | |
CNHFAHCC_02809 | 1.2e-145 | lacG | G | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_02810 | 2.3e-245 | S | Saccharopine dehydrogenase | |||
CNHFAHCC_02811 | 2.5e-146 | S | Protein of unknown function (DUF3153) | |||
CNHFAHCC_02812 | 3.6e-32 | natC | E | L-phenylalanine transmembrane transporter activity | ||
CNHFAHCC_02814 | 3.2e-164 | sitC | U | ABC 3 transport family | ||
CNHFAHCC_02815 | 1.9e-141 | sitB | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
CNHFAHCC_02816 | 1.2e-185 | sitA | P | Zinc-uptake complex component A periplasmic | ||
CNHFAHCC_02817 | 7.1e-32 | L | Transposase | |||
CNHFAHCC_02818 | 1.1e-53 | kaiB | T | PFAM KaiB domain | ||
CNHFAHCC_02819 | 0.0 | kaiC | T | Core component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. Binds to DNA. The KaiABC complex may act as a promoter-nonspecific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction | ||
CNHFAHCC_02820 | 5.9e-129 | S | Protein of unknown function (DUF4230) | |||
CNHFAHCC_02821 | 4.2e-175 | rbcR | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
CNHFAHCC_02822 | 5.6e-273 | P | Sodium/hydrogen exchanger family | |||
CNHFAHCC_02823 | 1.8e-113 | KT | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_02824 | 4.6e-194 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_02825 | 3.4e-305 | kdpA | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit binds and transports the potassium across the cytoplasmic membrane | |
CNHFAHCC_02826 | 0.0 | kdpB | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system | |
CNHFAHCC_02828 | 6.6e-99 | kdpC | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit acts as a catalytic chaperone that increases the ATP- binding affinity of the ATP-hydrolyzing subunit KdpB by the formation of a transient KdpB KdpC ATP ternary complex | |
CNHFAHCC_02829 | 4.1e-206 | T | Osmosensitive K channel histidine kinase KdpD | |||
CNHFAHCC_02830 | 0.0 | M | Domain of Unknown Function (DUF748) | |||
CNHFAHCC_02831 | 0.0 | crtU | H | Thi4 family | ||
CNHFAHCC_02832 | 4.1e-80 | |||||
CNHFAHCC_02833 | 3.6e-111 | cobO | 2.5.1.17 | H | Cob(I)alamin adenosyltransferase N terminal | |
CNHFAHCC_02834 | 3.3e-11 | |||||
CNHFAHCC_02835 | 4.7e-225 | spoIID | D | Stage II sporulation protein | ||
CNHFAHCC_02836 | 6.3e-237 | nuoD | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_02837 | 1.2e-65 | |||||
CNHFAHCC_02838 | 5.7e-49 | |||||
CNHFAHCC_02839 | 2.7e-204 | S | Alpha/beta hydrolase family | |||
CNHFAHCC_02840 | 1.1e-155 | L | Transposase | |||
CNHFAHCC_02841 | 1.7e-229 | coaBC | 4.1.1.36, 6.3.2.5 | F | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
CNHFAHCC_02842 | 1.7e-31 | S | Protein of unknown function (DUF2555) | |||
CNHFAHCC_02843 | 4.3e-146 | bioH | 3.1.1.85 | Q | Thioesterase involved in non-ribosomal peptide biosynthesis | |
CNHFAHCC_02844 | 8e-96 | fldA | C | Low-potential electron donor to a number of redox enzymes | ||
CNHFAHCC_02845 | 1e-198 | isiA | A | Photosystem II protein | ||
CNHFAHCC_02846 | 3.1e-153 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
CNHFAHCC_02847 | 1e-196 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
CNHFAHCC_02848 | 1.4e-197 | galE | 5.1.3.2 | M | RmlD substrate binding domain | |
CNHFAHCC_02849 | 2.9e-105 | |||||
CNHFAHCC_02850 | 3.3e-55 | S | Protein of unknown function (DUF2605) | |||
CNHFAHCC_02851 | 8.5e-24 | S | Phycobilisome degradation protein nblA | |||
CNHFAHCC_02852 | 1.3e-24 | S | Phycobilisome degradation protein nblA | |||
CNHFAHCC_02854 | 3.8e-187 | |||||
CNHFAHCC_02855 | 3.4e-156 | |||||
CNHFAHCC_02857 | 0.0 | iga | 3.4.24.13 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |
CNHFAHCC_02858 | 2.2e-137 | T | Two component regulator propeller | |||
CNHFAHCC_02859 | 4.9e-122 | potA_1 | 3.6.3.30 | P | ATPase activity | |
CNHFAHCC_02860 | 2e-302 | P | ABC-type Fe3 transport system permease component | |||
CNHFAHCC_02861 | 1.2e-191 | P | ABC-type Fe3 transport system, periplasmic component | |||
CNHFAHCC_02863 | 0.0 | E | Zn_pept | |||
CNHFAHCC_02864 | 2.5e-194 | glsA | 3.5.1.2 | E | Glutaminase | |
CNHFAHCC_02865 | 2e-36 | |||||
CNHFAHCC_02866 | 1.3e-86 | V | HNH endonuclease | |||
CNHFAHCC_02867 | 6.2e-154 | tyrA | 1.3.1.12, 1.3.1.43, 1.3.1.78 | E | Prephenate dehydrogenase | |
CNHFAHCC_02868 | 0.0 | 1.9.3.1 | C | Cytochrome C and Quinol oxidase polypeptide I | ||
CNHFAHCC_02869 | 2.7e-111 | ctaE | 1.9.3.1 | C | Cytochrome c oxidase subunit III | |
CNHFAHCC_02870 | 3.3e-126 | S | Putative restriction endonuclease | |||
CNHFAHCC_02871 | 9.9e-166 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
CNHFAHCC_02872 | 0.0 | katG | 1.11.1.21 | P | Bifunctional enzyme with both catalase and broad- spectrum peroxidase activity | |
CNHFAHCC_02873 | 1.6e-263 | ccs1 | O | Required during biogenesis of c-type cytochromes (cytochrome c6 and cytochrome f) at the step of heme attachment | ||
CNHFAHCC_02874 | 0.0 | ilvB | 2.2.1.6 | E | Thiamine pyrophosphate enzyme, central domain | |
CNHFAHCC_02875 | 0.0 | shc | 4.2.1.129, 5.4.99.17 | I | A-macroglobulin complement component | |
CNHFAHCC_02877 | 1.2e-25 | L | transposition | |||
CNHFAHCC_02878 | 8.2e-63 | L | transposition | |||
CNHFAHCC_02879 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_02880 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_02881 | 5.8e-126 | L | DDE superfamily endonuclease | |||
CNHFAHCC_02882 | 6e-29 | S | Putative restriction endonuclease | |||
CNHFAHCC_02883 | 2.5e-49 | S | Putative restriction endonuclease | |||
CNHFAHCC_02884 | 0.0 | ilvB | 2.2.1.6 | EH | Thiamine pyrophosphate enzyme, central domain | |
CNHFAHCC_02885 | 4.4e-30 | |||||
CNHFAHCC_02887 | 3.4e-97 | txlA | CO | Thioredoxin-like | ||
CNHFAHCC_02888 | 4.5e-76 | S | Tpr repeat-containing protein | |||
CNHFAHCC_02889 | 2.2e-193 | glpX | 3.1.3.11, 3.1.3.37 | G | Belongs to the FBPase class 2 family | |
CNHFAHCC_02890 | 1.1e-79 | L | PFAM IS1 transposase | |||
CNHFAHCC_02891 | 2.6e-64 | glbN | C | Group 1 truncated hemoglobin | ||
CNHFAHCC_02892 | 0.0 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_02893 | 3.4e-200 | 2.7.13.3, 4.6.1.1 | T | PhoQ Sensor | ||
CNHFAHCC_02894 | 6.8e-209 | T | COG3437 Response regulator containing a CheY-like receiver domain and an HD-GYP domain | |||
CNHFAHCC_02895 | 4.5e-76 | bacB | 5.3.3.19 | S | Cupin domain | |
CNHFAHCC_02896 | 9.8e-243 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
CNHFAHCC_02897 | 7.9e-176 | I | Diacylglycerol acyltransferase | |||
CNHFAHCC_02898 | 0.0 | 2.7.13.3, 3.1.3.3 | T | PhoQ Sensor | ||
CNHFAHCC_02899 | 2.7e-112 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
CNHFAHCC_02900 | 1.1e-301 | gldG | N | ABC-type uncharacterized transport system | ||
CNHFAHCC_02901 | 2.6e-94 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
CNHFAHCC_02902 | 1.5e-158 | V | Alternative locus ID | |||
CNHFAHCC_02903 | 2.8e-30 | L | recombinase activity | |||
CNHFAHCC_02904 | 2.2e-146 | S | Sodium Bile acid symporter family | |||
CNHFAHCC_02905 | 3.2e-194 | tas | 1.1.1.65 | C | Aldo/keto reductase family | |
CNHFAHCC_02906 | 9.6e-220 | hhoB | 3.4.21.107 | O | Trypsin | |
CNHFAHCC_02907 | 6.8e-86 | |||||
CNHFAHCC_02908 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
CNHFAHCC_02909 | 1.7e-105 | S | Late competence development protein ComFB | |||
CNHFAHCC_02910 | 3.2e-145 | sll1424 | S | Protein of unknown function (DUF3084) | ||
CNHFAHCC_02911 | 1.8e-119 | ntcA | K | helix_turn_helix, cAMP Regulatory protein | ||
CNHFAHCC_02912 | 8.8e-40 | |||||
CNHFAHCC_02913 | 0.0 | S | Platelet-activating factor acetylhydrolase, isoform II | |||
CNHFAHCC_02915 | 1.2e-204 | hpnH | S | Domain of unknown function (DUF3463) | ||
CNHFAHCC_02916 | 1e-223 | rfaG | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
CNHFAHCC_02917 | 3.8e-238 | trkH | P | Cation transport protein | ||
CNHFAHCC_02918 | 2.7e-191 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
CNHFAHCC_02919 | 8.3e-166 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
CNHFAHCC_02920 | 1e-99 | psbP | S | PsbP | ||
CNHFAHCC_02921 | 1.9e-198 | sbtA | S | Na+-dependent bicarbonate transporter superfamily | ||
CNHFAHCC_02922 | 1.7e-54 | E | Belongs to the P(II) protein family | |||
CNHFAHCC_02923 | 7.2e-180 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
CNHFAHCC_02924 | 2.7e-121 | thf1 | A | May be involved in photosynthetic membrane biogenesis | ||
CNHFAHCC_02925 | 2.2e-18 | |||||
CNHFAHCC_02926 | 9.5e-272 | ictB | M | O-Antigen ligase | ||
CNHFAHCC_02927 | 1.6e-45 | S | Protein of unknown function (DUF3288) | |||
CNHFAHCC_02928 | 5.3e-115 | sodB | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
CNHFAHCC_02929 | 1.3e-201 | leuB | 1.1.1.85 | E | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
CNHFAHCC_02930 | 8.2e-44 | |||||
CNHFAHCC_02931 | 2.5e-172 | menA | 2.5.1.74 | H | Involved in the synthesis of phylloquinone (vitamin K1). Catalyzes the transfer of a prenyl chain to 2-carboxy-1,4- naphthoquinone | |
CNHFAHCC_02932 | 2.5e-42 | hglK | S | Pentapeptide repeats (9 copies) | ||
CNHFAHCC_02933 | 4.7e-210 | S | 4Fe-4S dicluster domain | |||
CNHFAHCC_02934 | 3.9e-290 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
CNHFAHCC_02936 | 8.1e-207 | L | DDE superfamily endonuclease | |||
CNHFAHCC_02937 | 4.6e-22 | L | transposition | |||
CNHFAHCC_02938 | 4.3e-126 | L | HTH-like domain | |||
CNHFAHCC_02939 | 3.1e-87 | L | Transposase | |||
CNHFAHCC_02940 | 8.5e-50 | L | Transposase | |||
CNHFAHCC_02941 | 1.9e-192 | 2.6.1.102 | M | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
CNHFAHCC_02942 | 9.9e-307 | 2.4.1.182 | GT19 | M | Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell | |
CNHFAHCC_02943 | 2.6e-157 | M | glycosyl transferase | |||
CNHFAHCC_02944 | 1.2e-100 | S | Protein of unknown function DUF115 | |||
CNHFAHCC_02945 | 3.4e-12 | S | Protein of unknown function DUF115 | |||
CNHFAHCC_02946 | 8.4e-248 | M | transferase activity, transferring glycosyl groups | |||
CNHFAHCC_02947 | 2e-165 | H | protein methyltransferase activity | |||
CNHFAHCC_02948 | 9.4e-194 | GT2 | M | Glycosyl transferase family 2 | ||
CNHFAHCC_02949 | 2e-120 | 3.5.1.9 | S | Putative cyclase | ||
CNHFAHCC_02950 | 8.9e-127 | 2.7.7.43 | M | Cytidylyltransferase | ||
CNHFAHCC_02951 | 8.8e-181 | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
CNHFAHCC_02952 | 1.5e-135 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_02953 | 1.5e-154 | S | Protein of unknown function DUF115 | |||
CNHFAHCC_02954 | 2.7e-165 | S | Glycosyltransferase like family 2 | |||
CNHFAHCC_02956 | 9.6e-90 | S | ATPase (AAA superfamily | |||
CNHFAHCC_02957 | 2.6e-82 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_02958 | 6.3e-184 | M | Glycosyl transferase family 2 | |||
CNHFAHCC_02959 | 5.5e-186 | hemB | 4.2.1.24 | H | Delta-aminolevulinic acid dehydratase | |
CNHFAHCC_02961 | 2.3e-201 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
CNHFAHCC_02962 | 0.0 | U | Protein export membrane protein | |||
CNHFAHCC_02963 | 3.5e-11 | |||||
CNHFAHCC_02964 | 5e-31 | S | PIN domain | |||
CNHFAHCC_02965 | 5.8e-111 | |||||
CNHFAHCC_02966 | 9.4e-83 | |||||
CNHFAHCC_02967 | 9.9e-80 | |||||
CNHFAHCC_02968 | 2e-280 | tldD | S | Putative modulator of DNA gyrase | ||
CNHFAHCC_02969 | 9.8e-174 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
CNHFAHCC_02970 | 7.3e-225 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_02971 | 5.2e-27 | |||||
CNHFAHCC_02972 | 1.3e-53 | |||||
CNHFAHCC_02973 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | F | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
CNHFAHCC_02974 | 3.7e-243 | ahcY | 3.3.1.1 | F | May play a key role in the regulation of the intracellular concentration of adenosylhomocysteine | |
CNHFAHCC_02975 | 2.9e-31 | |||||
CNHFAHCC_02976 | 1.9e-74 | S | PIN domain | |||
CNHFAHCC_02977 | 7.4e-174 | E | Bacterial transglutaminase-like N-terminal region | |||
CNHFAHCC_02978 | 1.6e-105 | S | Putative restriction endonuclease | |||
CNHFAHCC_02979 | 1.4e-215 | mtfB | 2.4.1.349 | GT4 | M | Glycosyl transferases group 1 |
CNHFAHCC_02980 | 3.6e-205 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_02981 | 0.0 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |||
CNHFAHCC_02982 | 3.3e-272 | atpD | 3.6.3.14 | F | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
CNHFAHCC_02983 | 2.8e-67 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
CNHFAHCC_02984 | 3.2e-286 | ymxG | S | Peptidase M16 inactive domain | ||
CNHFAHCC_02985 | 2e-238 | fabF2 | 2.3.1.179, 2.3.1.41 | IQ | Beta-ketoacyl synthase, N-terminal domain | |
CNHFAHCC_02986 | 2.4e-283 | hoxH | 1.12.1.2 | C | Nickel-dependent hydrogenase | |
CNHFAHCC_02987 | 7e-80 | S | Toxic component of a toxin-antitoxin (TA) module. An RNase | |||
CNHFAHCC_02988 | 2.2e-38 | |||||
CNHFAHCC_02989 | 1.6e-102 | hoxY | 1.12.1.2 | C | NADH ubiquinone oxidoreductase, 20 Kd subunit | |
CNHFAHCC_02990 | 2e-137 | hoxU | 1.17.1.10, 1.6.5.3 | C | 4Fe-4S binding domain | |
CNHFAHCC_02991 | 3.6e-122 | S | Putative restriction endonuclease | |||
CNHFAHCC_02992 | 0.0 | hoxF | 1.12.1.3, 1.6.5.3 | C | NADH-ubiquinone oxidoreductase-F iron-sulfur binding region | |
CNHFAHCC_02993 | 6.9e-95 | hoxE | 1.6.5.3 | C | Thioredoxin-like [2Fe-2S] ferredoxin | |
CNHFAHCC_02995 | 2.3e-37 | L | Transposase | |||
CNHFAHCC_02996 | 1.5e-283 | femD | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, C-terminal domain | |
CNHFAHCC_02997 | 1.8e-56 | |||||
CNHFAHCC_02998 | 1.9e-118 | GM | NmrA-like family | |||
CNHFAHCC_02999 | 1.1e-129 | ung2 | 3.2.2.27 | L | Uracil DNA glycosylase superfamily | |
CNHFAHCC_03000 | 2.3e-27 | |||||
CNHFAHCC_03001 | 4.9e-176 | dacB | 3.4.16.4 | M | Beta-lactamase enzyme family | |
CNHFAHCC_03002 | 7.7e-252 | 1.1.3.15 | C | FAD binding domain | ||
CNHFAHCC_03003 | 3.1e-14 | psaJ | U | May help in the organization of the PsaE and PsaF subunits | ||
CNHFAHCC_03004 | 2.6e-91 | psaF | S | Photosystem I reaction centre subunit III | ||
CNHFAHCC_03005 | 2.5e-197 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
CNHFAHCC_03006 | 1.2e-100 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
CNHFAHCC_03007 | 8.5e-195 | uxs | 4.1.1.35, 4.2.1.46 | M | Male sterility protein | |
CNHFAHCC_03008 | 5.5e-59 | S | Domain of unknown function (DUF4351) | |||
CNHFAHCC_03009 | 3.7e-151 | rsmI | 2.1.1.198 | J | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
CNHFAHCC_03010 | 4.3e-33 | |||||
CNHFAHCC_03011 | 3.9e-170 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
CNHFAHCC_03012 | 5.8e-216 | mviM | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
CNHFAHCC_03013 | 9.3e-147 | O | SPFH domain Band 7 family | |||
CNHFAHCC_03014 | 1.9e-169 | cruF | S | Carotenoid biosynthesis protein | ||
CNHFAHCC_03015 | 1.1e-161 | coxM | 1.9.3.1 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
CNHFAHCC_03016 | 7.8e-151 | coaX | 2.7.1.33, 6.3.4.15 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
CNHFAHCC_03017 | 3.1e-228 | ugcG | 2.4.1.80 | GT21 | M | Glycosyl transferase family group 2 |
CNHFAHCC_03018 | 3.8e-73 | |||||
CNHFAHCC_03019 | 1.2e-33 | ndhL | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient | |
CNHFAHCC_03020 | 4.1e-50 | slr0815 | S | Protein of unknown function (DUF3007) | ||
CNHFAHCC_03021 | 1e-95 | yceD | S | Uncharacterized ACR, COG1399 | ||
CNHFAHCC_03022 | 2.4e-42 | L | PFAM Transposase DDE domain | |||
CNHFAHCC_03023 | 2.3e-104 | tnpA | L | DDE superfamily endonuclease | ||
CNHFAHCC_03024 | 1.3e-131 | lipM | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
CNHFAHCC_03026 | 9.1e-275 | menF | 5.4.4.2 | HQ | chorismate binding enzyme | |
CNHFAHCC_03027 | 7.9e-244 | S | Tetratricopeptide repeat | |||
CNHFAHCC_03028 | 2.2e-311 | lnt | GT2 | M | Transfers the fatty acyl group on membrane lipoproteins | |
CNHFAHCC_03029 | 1.1e-43 | XAC3035 | O | Glutaredoxin-like domain (DUF836) | ||
CNHFAHCC_03030 | 2.8e-279 | M | Bacterial sugar transferase | |||
CNHFAHCC_03031 | 1.2e-31 | L | DDE superfamily endonuclease | |||
CNHFAHCC_03032 | 2.5e-98 | L | Transposase | |||
CNHFAHCC_03033 | 1.7e-44 | cysO | 2.7.7.80, 2.8.1.11 | H | ThiS family | |
CNHFAHCC_03034 | 7.4e-129 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
CNHFAHCC_03035 | 0.0 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | ||
CNHFAHCC_03036 | 1.1e-79 | S | for the assembly of the photosystem I | |||
CNHFAHCC_03037 | 1.8e-251 | ycjF | S | TIGRFAM Small GTP-binding protein | ||
CNHFAHCC_03038 | 1.8e-86 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_03039 | 1.8e-80 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_03040 | 2.5e-23 | |||||
CNHFAHCC_03041 | 2.1e-171 | fieF | U | Dimerisation domain of Zinc Transporter | ||
CNHFAHCC_03042 | 6.4e-87 | ndhN | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_03043 | 9.8e-115 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
CNHFAHCC_03044 | 2.3e-145 | rpsB | J | Ribosomal protein S2 | ||
CNHFAHCC_03046 | 1.9e-195 | cax | P | Sodium/calcium exchanger protein | ||
CNHFAHCC_03047 | 1.4e-109 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
CNHFAHCC_03048 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_03049 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_03050 | 1.5e-106 | S | vWA found in TerF C terminus | |||
CNHFAHCC_03051 | 3.3e-08 | |||||
CNHFAHCC_03052 | 4.4e-97 | MA20_02285 | 2.3.1.57 | K | -acetyltransferase | |
CNHFAHCC_03053 | 3.8e-190 | L | PFAM Transposase | |||
CNHFAHCC_03054 | 2.4e-184 | S | Domain of unknown function DUF21 | |||
CNHFAHCC_03055 | 3.5e-252 | S | Putative nucleotide-binding of sugar-metabolising enzyme | |||
CNHFAHCC_03056 | 5.5e-310 | phrB | S | Deoxyribodipyrimidine photo-lyase-related protein | ||
CNHFAHCC_03057 | 0.0 | cca | 2.7.7.19, 2.7.7.72, 3.1.13.3, 3.1.3.7 | J | Poly A polymerase head domain | |
CNHFAHCC_03058 | 2.3e-139 | ylmH | 5.4.99.23, 5.4.99.24 | S | S4 RNA-binding domain | |
CNHFAHCC_03059 | 6.5e-151 | ttg2B | Q | Permease MlaE | ||
CNHFAHCC_03060 | 1.3e-56 | L | Tetratricopeptide repeat | |||
CNHFAHCC_03061 | 9.8e-24 | S | protein conserved in cyanobacteria | |||
CNHFAHCC_03062 | 2e-64 | S | COGs COG4636 conserved | |||
CNHFAHCC_03063 | 1.2e-285 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Pantoate-beta-alanine ligase | |
CNHFAHCC_03064 | 1.6e-182 | 4.2.1.1 | P | Carbonic anhydrase | ||
CNHFAHCC_03065 | 6.6e-123 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
CNHFAHCC_03066 | 9.2e-308 | pgi | 5.3.1.9 | F | Phosphoglucose isomerase | |
CNHFAHCC_03067 | 7.1e-216 | desA | 1.14.19.23, 1.14.19.45 | I | Fatty acid desaturase | |
CNHFAHCC_03068 | 3.1e-245 | S | PFAM Archaeal ATPase | |||
CNHFAHCC_03069 | 9.1e-256 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
CNHFAHCC_03070 | 1.3e-66 | cytM | C | Cytochrome C oxidase, cbb3-type, subunit III | ||
CNHFAHCC_03071 | 1.2e-83 | rplI | J | Ribosomal protein L9, N-terminal domain | ||
CNHFAHCC_03072 | 6.2e-125 | |||||
CNHFAHCC_03073 | 0.0 | MA20_17485 | C | cobalamin binding | ||
CNHFAHCC_03074 | 1.5e-57 | S | Tetratricopeptide repeat | |||
CNHFAHCC_03075 | 1.7e-56 | L | nUDIX hydrolase | |||
CNHFAHCC_03076 | 1.5e-101 | KLT | GUN4-like | |||
CNHFAHCC_03077 | 9.4e-123 | vatD | S | Bacterial transferase hexapeptide (six repeats) | ||
CNHFAHCC_03078 | 4.3e-33 | hypC | O | HupF/HypC family | ||
CNHFAHCC_03079 | 4e-167 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
CNHFAHCC_03080 | 6.4e-176 | ctaA | O | Cytochrome oxidase assembly protein | ||
CNHFAHCC_03081 | 0.0 | 2.7.7.7, 3.6.4.12 | LO | EXOIII | ||
CNHFAHCC_03082 | 5.3e-77 | S | EVE domain | |||
CNHFAHCC_03083 | 1.6e-51 | L | DDE superfamily endonuclease | |||
CNHFAHCC_03084 | 2.6e-48 | D | protein conserved in cyanobacteria | |||
CNHFAHCC_03085 | 6.4e-215 | Q | Part of the tripartite ATP-independent periplasmic (TRAP) transport system | |||
CNHFAHCC_03086 | 1.5e-134 | T | Forkhead associated domain | |||
CNHFAHCC_03087 | 2.9e-63 | mbeC | S | Psort location Cytoplasmic, score | ||
CNHFAHCC_03088 | 1.2e-214 | tetA | EGP | Sugar (and other) transporter | ||
CNHFAHCC_03089 | 1.2e-242 | tetL | EGP | Major Facilitator Superfamily | ||
CNHFAHCC_03090 | 2e-160 | penP | 3.5.2.6 | V | Beta-lactamase | |
CNHFAHCC_03091 | 6.6e-162 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
CNHFAHCC_03092 | 2.5e-228 | proA | 1.2.1.41, 1.2.1.81 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
CNHFAHCC_03093 | 1.3e-70 | ohrA | O | Organic hydroperoxide resistance protein | ||
CNHFAHCC_03094 | 3.9e-75 | ohrR | K | COG1846 Transcriptional regulators | ||
CNHFAHCC_03095 | 8.4e-72 | ohrB | O | Organic hydroperoxide resistance protein | ||
CNHFAHCC_03097 | 2.8e-87 | guaD | 3.5.4.12, 3.5.4.3, 3.5.4.33 | FJ | COG0590 Cytosine adenosine deaminases | |
CNHFAHCC_03098 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
CNHFAHCC_03099 | 1.7e-176 | isp | O | Belongs to the peptidase S8 family | ||
CNHFAHCC_03100 | 6.3e-151 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
CNHFAHCC_03101 | 1.8e-136 | ykoC | P | Cobalt transport protein | ||
CNHFAHCC_03102 | 4.6e-311 | P | ABC transporter, ATP-binding protein | |||
CNHFAHCC_03103 | 6.9e-99 | ykoE | S | ABC-type cobalt transport system, permease component | ||
CNHFAHCC_03104 | 7.9e-111 | ykoF | S | YKOF-related Family | ||
CNHFAHCC_03105 | 2.4e-124 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_03106 | 9.4e-245 | ykoH | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_03107 | 1.1e-113 | ykoI | S | Peptidase propeptide and YPEB domain | ||
CNHFAHCC_03108 | 4.4e-86 | ykoJ | S | Peptidase propeptide and YPEB domain | ||
CNHFAHCC_03111 | 2.2e-222 | mgtE | P | Acts as a magnesium transporter | ||
CNHFAHCC_03112 | 1.4e-53 | tnrA | K | transcriptional | ||
CNHFAHCC_03113 | 5.9e-18 | |||||
CNHFAHCC_03114 | 6.9e-26 | ykoL | ||||
CNHFAHCC_03115 | 1.3e-81 | mhqR | K | transcriptional | ||
CNHFAHCC_03116 | 2.3e-220 | ugtP | 2.4.1.315 | GT28 | M | COG0707 UDP-N-acetylglucosamine LPS N-acetylglucosamine transferase |
CNHFAHCC_03117 | 3.7e-99 | ykoP | G | polysaccharide deacetylase | ||
CNHFAHCC_03118 | 7.1e-155 | ykoQ | S | Calcineurin-like phosphoesterase superfamily domain | ||
CNHFAHCC_03119 | 0.0 | ykoS | ||||
CNHFAHCC_03120 | 2.5e-186 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
CNHFAHCC_03121 | 0.0 | ligD | 6.5.1.1 | L | ATP-dependent DNA ligase | |
CNHFAHCC_03122 | 7.3e-172 | ku | L | With LigD forms a non-homologous end joining (NHEJ) DNA repair enzyme, which repairs dsDNA breaks with reduced fidelity. Binds linear dsDNA with 5'- and 3'- overhangs but not closed circular dsDNA nor ssDNA. Recruits and stimulates the ligase activity of LigD | ||
CNHFAHCC_03123 | 0.0 | ydcR | 2.7.7.65 | T | Diguanylate cyclase | |
CNHFAHCC_03124 | 1.4e-116 | ykoX | S | membrane-associated protein | ||
CNHFAHCC_03125 | 2.1e-177 | ykoY | P | COG0861 Membrane protein TerC, possibly involved in tellurium resistance | ||
CNHFAHCC_03126 | 9.5e-130 | sigI | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_03127 | 8.2e-117 | rsgI | S | Anti-sigma factor N-terminus | ||
CNHFAHCC_03128 | 1.9e-26 | sspD | S | small acid-soluble spore protein | ||
CNHFAHCC_03129 | 1.5e-124 | ykrK | S | Domain of unknown function (DUF1836) | ||
CNHFAHCC_03130 | 7e-156 | htpX | O | Belongs to the peptidase M48B family | ||
CNHFAHCC_03131 | 1.7e-233 | ktrB | P | COG0168 Trk-type K transport systems, membrane components | ||
CNHFAHCC_03132 | 1.2e-10 | ydfR | S | Protein of unknown function (DUF421) | ||
CNHFAHCC_03133 | 4.5e-22 | ykzE | ||||
CNHFAHCC_03134 | 6.5e-190 | ykrP | G | COG3594 Fucose 4-O-acetylase and related acetyltransferases | ||
CNHFAHCC_03135 | 0.0 | kinE | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_03136 | 7e-89 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
CNHFAHCC_03137 | 3.3e-197 | mtnA | 5.3.1.23 | E | Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P) | |
CNHFAHCC_03138 | 7.5e-230 | mtnK | 2.7.1.100 | F | Catalyzes the phosphorylation of methylthioribose into methylthioribose-1-phosphate | |
CNHFAHCC_03139 | 3.5e-151 | mtnU | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
CNHFAHCC_03140 | 8e-232 | mtnE | 2.6.1.83 | E | Aminotransferase | |
CNHFAHCC_03141 | 4.1e-231 | mtnW | 5.3.2.5 | G | Catalyzes the enolization of 2,3-diketo-5- methylthiopentyl-1-phosphate (DK-MTP-1-P) into 2-hydroxy-3-keto-5- methylthiopentenyl-1-phosphate (HK-MTPenyl-1-P) | |
CNHFAHCC_03142 | 7.5e-137 | mtnX | 3.1.3.87, 4.2.1.109 | E | Dephosphorylates 2-hydroxy-3-keto-5-methylthiopentenyl- 1-phosphate (HK-MTPenyl-1-P) yielding 1,2-dihydroxy-3-keto-5- methylthiopentene (DHK-MTPene) | |
CNHFAHCC_03143 | 7.2e-115 | mtnB | 3.1.3.87, 4.1.2.17, 4.2.1.109, 5.1.3.4 | E | Catalyzes the dehydration of methylthioribulose-1- phosphate (MTRu-1-P) into 2,3-diketo-5-methylthiopentyl-1- phosphate (DK-MTP-1-P) | |
CNHFAHCC_03144 | 1.3e-96 | mtnD | 1.13.11.53, 1.13.11.54 | S | Catalyzes 2 different reactions between oxygene and the acireductone 1,2-dihydroxy-3-keto-5-methylthiopentene (DHK-MTPene) depending upon the metal bound in the active site. Fe-containing acireductone dioxygenase (Fe-ARD) produces formate and 2-keto-4- methylthiobutyrate (KMTB), the alpha-ketoacid precursor of methionine in the methionine recycle pathway. Ni-containing acireductone dioxygenase (Ni-ARD) produces methylthiopropionate, carbon monoxide and formate, and does not lie on the methionine recycle pathway | |
CNHFAHCC_03145 | 1.3e-51 | XK27_09985 | S | Protein of unknown function (DUF1232) | ||
CNHFAHCC_03146 | 6.4e-09 | S | Spo0E like sporulation regulatory protein | |||
CNHFAHCC_03147 | 1.4e-64 | eag | ||||
CNHFAHCC_03148 | 2.9e-279 | kinD | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
CNHFAHCC_03149 | 1.3e-75 | ykvE | K | transcriptional | ||
CNHFAHCC_03150 | 2.5e-125 | motB | N | Flagellar motor protein | ||
CNHFAHCC_03151 | 3e-138 | motA | N | flagellar motor | ||
CNHFAHCC_03152 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
CNHFAHCC_03153 | 8.7e-182 | ykvI | S | membrane | ||
CNHFAHCC_03154 | 7.3e-126 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
CNHFAHCC_03155 | 2.8e-81 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
CNHFAHCC_03156 | 1.3e-139 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
CNHFAHCC_03157 | 2e-96 | queF | 1.7.1.13 | S | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
CNHFAHCC_03158 | 2e-61 | ykvN | K | Transcriptional regulator | ||
CNHFAHCC_03159 | 8.2e-134 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_03160 | 1.3e-234 | ykvP | 3.5.1.28 | M | Glycosyl transferases group 1 | |
CNHFAHCC_03161 | 1.2e-35 | 3.5.1.104 | M | LysM domain | ||
CNHFAHCC_03162 | 8.5e-133 | G | Glycosyl hydrolases family 18 | |||
CNHFAHCC_03164 | 5.6e-46 | ykvR | S | Protein of unknown function (DUF3219) | ||
CNHFAHCC_03165 | 6e-25 | ykvS | S | protein conserved in bacteria | ||
CNHFAHCC_03166 | 2.8e-28 | |||||
CNHFAHCC_03167 | 1.7e-103 | ykvT | 3.5.1.28 | M | Cell Wall Hydrolase | |
CNHFAHCC_03168 | 9.9e-239 | ykvU | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
CNHFAHCC_03169 | 4.9e-90 | stoA | CO | thiol-disulfide | ||
CNHFAHCC_03170 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
CNHFAHCC_03171 | 8.7e-209 | pepQ | 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
CNHFAHCC_03173 | 9.8e-180 | ykvZ | 5.1.1.1 | K | Transcriptional regulator | |
CNHFAHCC_03174 | 4.5e-128 | glcT | K | antiterminator | ||
CNHFAHCC_03175 | 0.0 | ptsG | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_03176 | 2.1e-39 | ptsH | G | phosphocarrier protein HPr | ||
CNHFAHCC_03177 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
CNHFAHCC_03178 | 7.2e-39 | splA | S | Transcriptional regulator | ||
CNHFAHCC_03179 | 2.6e-202 | splB | 4.1.99.14 | L | Spore photoproduct lyase | |
CNHFAHCC_03180 | 1.2e-131 | ykwB | 2.3.1.1 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
CNHFAHCC_03181 | 2e-264 | mcpC | NT | chemotaxis protein | ||
CNHFAHCC_03182 | 5e-159 | glxR | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
CNHFAHCC_03183 | 8e-124 | ykwD | J | protein with SCP PR1 domains | ||
CNHFAHCC_03184 | 0.0 | mrdA | 3.4.16.4 | M | Penicillin-binding Protein | |
CNHFAHCC_03185 | 0.0 | pilS | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_03186 | 8e-224 | patA | 2.6.1.1 | E | Aminotransferase | |
CNHFAHCC_03187 | 2.2e-15 | |||||
CNHFAHCC_03188 | 1.6e-168 | cheV | 2.7.13.3 | T | Chemotaxis protein CheV | |
CNHFAHCC_03189 | 1.7e-84 | ykyB | S | YkyB-like protein | ||
CNHFAHCC_03190 | 1.6e-238 | ykuC | EGP | Major facilitator Superfamily | ||
CNHFAHCC_03191 | 4.6e-88 | ykuD | S | protein conserved in bacteria | ||
CNHFAHCC_03192 | 9.4e-166 | ykuE | S | Metallophosphoesterase | ||
CNHFAHCC_03193 | 2.2e-142 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_03194 | 0.0 | 3.2.1.132 | M | Putative peptidoglycan binding domain | ||
CNHFAHCC_03195 | 1.4e-102 | M | Peptidoglycan-binding domain 1 protein | |||
CNHFAHCC_03197 | 5.2e-234 | ykuI | T | Diguanylate phosphodiesterase | ||
CNHFAHCC_03199 | 3.9e-37 | ykuJ | S | protein conserved in bacteria | ||
CNHFAHCC_03200 | 4.4e-94 | ykuK | S | Ribonuclease H-like | ||
CNHFAHCC_03201 | 3.9e-27 | ykzF | S | Antirepressor AbbA | ||
CNHFAHCC_03202 | 1.6e-76 | ykuL | S | CBS domain | ||
CNHFAHCC_03203 | 3.5e-168 | ccpC | K | Transcriptional regulator | ||
CNHFAHCC_03204 | 5.7e-88 | fld | C | Flavodoxin domain | ||
CNHFAHCC_03205 | 3.2e-177 | ykuO | ||||
CNHFAHCC_03206 | 3.2e-80 | fld | C | Flavodoxin | ||
CNHFAHCC_03207 | 1.1e-74 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
CNHFAHCC_03208 | 5.8e-216 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
CNHFAHCC_03209 | 9e-37 | ykuS | S | Belongs to the UPF0180 family | ||
CNHFAHCC_03210 | 8.8e-142 | ykuT | M | Mechanosensitive ion channel | ||
CNHFAHCC_03211 | 3.9e-101 | ykuU | O | Alkyl hydroperoxide reductase | ||
CNHFAHCC_03212 | 4.4e-82 | ykuV | CO | thiol-disulfide | ||
CNHFAHCC_03213 | 5.8e-95 | rok | K | Repressor of ComK | ||
CNHFAHCC_03214 | 2.9e-147 | yknT | ||||
CNHFAHCC_03215 | 3.9e-110 | mobA | 2.7.7.77 | H | Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor | |
CNHFAHCC_03216 | 5.3e-192 | moeB | 2.7.7.73, 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
CNHFAHCC_03217 | 8.1e-246 | moeA | 2.10.1.1 | H | molybdopterin | |
CNHFAHCC_03218 | 9.9e-94 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
CNHFAHCC_03219 | 8.5e-84 | moaE | 2.8.1.12 | H | COG0314 Molybdopterin converting factor, large subunit | |
CNHFAHCC_03220 | 2.8e-32 | moaD | 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
CNHFAHCC_03221 | 0.0 | yknU | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
CNHFAHCC_03222 | 0.0 | yknV | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
CNHFAHCC_03223 | 1e-117 | yknW | S | Yip1 domain | ||
CNHFAHCC_03224 | 3e-159 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
CNHFAHCC_03225 | 2.5e-124 | macB | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_03226 | 2.1e-211 | yknZ | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
CNHFAHCC_03227 | 3.1e-136 | fruR | K | Transcriptional regulator | ||
CNHFAHCC_03228 | 6.2e-168 | fruK | 2.7.1.11, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
CNHFAHCC_03229 | 0.0 | fruA | 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
CNHFAHCC_03230 | 4.8e-105 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CNHFAHCC_03231 | 8.1e-39 | ykoA | ||||
CNHFAHCC_03232 | 5.8e-310 | ybiT | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
CNHFAHCC_03233 | 1.5e-169 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
CNHFAHCC_03234 | 2e-238 | ampS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
CNHFAHCC_03235 | 1.1e-12 | S | Uncharacterized protein YkpC | |||
CNHFAHCC_03236 | 7.6e-183 | mreB | D | Rod-share determining protein MreBH | ||
CNHFAHCC_03237 | 1.5e-43 | abrB | K | of stationary sporulation gene expression | ||
CNHFAHCC_03238 | 1.3e-241 | kinC | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
CNHFAHCC_03239 | 1.6e-162 | ykqA | P | Gamma-glutamyl cyclotransferase, AIG2-like | ||
CNHFAHCC_03240 | 4e-116 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
CNHFAHCC_03241 | 0.0 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
CNHFAHCC_03242 | 0.0 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
CNHFAHCC_03243 | 8.2e-31 | ykzG | S | Belongs to the UPF0356 family | ||
CNHFAHCC_03244 | 1.4e-147 | ykrA | S | hydrolases of the HAD superfamily | ||
CNHFAHCC_03245 | 4e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
CNHFAHCC_03247 | 2.8e-115 | recN | L | Putative cell-wall binding lipoprotein | ||
CNHFAHCC_03248 | 9.9e-192 | pdhA | 1.2.4.1, 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
CNHFAHCC_03249 | 2.9e-179 | pdhB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
CNHFAHCC_03250 | 9.9e-231 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
CNHFAHCC_03251 | 2.4e-243 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
CNHFAHCC_03252 | 1.3e-63 | slp | CO | COG0526, thiol-disulfide isomerase and thioredoxins | ||
CNHFAHCC_03253 | 3.5e-277 | speA | 4.1.1.19 | E | Arginine | |
CNHFAHCC_03254 | 1.6e-42 | yktA | S | Belongs to the UPF0223 family | ||
CNHFAHCC_03255 | 7.1e-118 | yktB | S | Belongs to the UPF0637 family | ||
CNHFAHCC_03256 | 7.1e-26 | ykzI | ||||
CNHFAHCC_03257 | 4.6e-151 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
CNHFAHCC_03258 | 6.9e-78 | ykzC | S | Acetyltransferase (GNAT) family | ||
CNHFAHCC_03259 | 6.5e-173 | Q | Exhibits S-adenosyl-L-methionine-dependent methyltransferase activity | |||
CNHFAHCC_03260 | 2.2e-293 | mpl | 3.4.24.28, 3.4.24.29 | E | Peptidase M4 | |
CNHFAHCC_03261 | 0.0 | ylaA | ||||
CNHFAHCC_03262 | 2.7e-42 | ylaB | ||||
CNHFAHCC_03263 | 2.7e-91 | ylaC | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_03264 | 1.2e-11 | sigC | S | Putative zinc-finger | ||
CNHFAHCC_03265 | 1.8e-38 | ylaE | ||||
CNHFAHCC_03266 | 8.2e-22 | S | Family of unknown function (DUF5325) | |||
CNHFAHCC_03267 | 0.0 | typA | T | GTP-binding protein TypA | ||
CNHFAHCC_03268 | 4.2e-47 | ylaH | S | YlaH-like protein | ||
CNHFAHCC_03269 | 2.5e-32 | ylaI | S | protein conserved in bacteria | ||
CNHFAHCC_03270 | 1.1e-89 | ylaJ | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
CNHFAHCC_03271 | 8e-249 | phoH | T | ATPase related to phosphate starvation-inducible protein PhoH | ||
CNHFAHCC_03272 | 2.7e-85 | ylaL | S | Part of the MsrPQ system that repairs oxidized periplasmic proteins containing methionine sulfoxide residues (Met-O), using respiratory chain electrons. Thus protects these proteins from oxidative-stress damage caused by reactive species of oxygen and chlorine generated by the host defense mechanisms. MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation. The catalytic subunit MsrP is non-stereospecific, being able to reduce both (R-) and (S-) diastereoisomers of methionine sulfoxide | ||
CNHFAHCC_03273 | 1.6e-171 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
CNHFAHCC_03274 | 8.7e-44 | ylaN | S | Belongs to the UPF0358 family | ||
CNHFAHCC_03275 | 4.5e-214 | ftsW | D | Belongs to the SEDS family | ||
CNHFAHCC_03276 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
CNHFAHCC_03277 | 2.6e-166 | ctaA | 2.5.1.141 | O | Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group | |
CNHFAHCC_03278 | 3.2e-164 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
CNHFAHCC_03279 | 6.2e-191 | ctaC | 1.9.3.1 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
CNHFAHCC_03280 | 0.0 | ctaD | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
CNHFAHCC_03281 | 3.3e-112 | cyoC | 1.10.3.12, 1.9.3.1 | C | COG1845 Heme copper-type cytochrome quinol oxidase, subunit 3 | |
CNHFAHCC_03282 | 4.2e-53 | ctaF | 1.10.3.12, 1.9.3.1 | C | COG3125 Heme copper-type cytochrome quinol oxidase, subunit 4 | |
CNHFAHCC_03283 | 3e-167 | ctaG | S | cytochrome c oxidase | ||
CNHFAHCC_03284 | 7e-62 | ylbA | S | YugN-like family | ||
CNHFAHCC_03285 | 2.6e-74 | ylbB | T | COG0517 FOG CBS domain | ||
CNHFAHCC_03286 | 3e-201 | ylbC | S | protein with SCP PR1 domains | ||
CNHFAHCC_03287 | 4.1e-63 | ylbD | S | Putative coat protein | ||
CNHFAHCC_03288 | 6.7e-37 | ylbE | S | YlbE-like protein | ||
CNHFAHCC_03289 | 1.8e-75 | ylbF | S | Belongs to the UPF0342 family | ||
CNHFAHCC_03290 | 7.5e-39 | ylbG | S | UPF0298 protein | ||
CNHFAHCC_03291 | 1.9e-98 | rsmD | 2.1.1.171 | L | Methyltransferase | |
CNHFAHCC_03292 | 3.9e-84 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
CNHFAHCC_03293 | 3.8e-221 | ylbJ | S | Sporulation integral membrane protein YlbJ | ||
CNHFAHCC_03294 | 7.5e-138 | ylbK | S | esterase of the alpha-beta hydrolase superfamily | ||
CNHFAHCC_03295 | 6.8e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
CNHFAHCC_03296 | 2.8e-235 | ylbM | S | Belongs to the UPF0348 family | ||
CNHFAHCC_03298 | 1.3e-90 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
CNHFAHCC_03299 | 1.2e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
CNHFAHCC_03300 | 6.8e-75 | ylbO | S | SANT SWI3, ADA2, N-CoR and TFIIIB'' DNA-binding domains | ||
CNHFAHCC_03301 | 4.7e-89 | ylbP | K | n-acetyltransferase | ||
CNHFAHCC_03302 | 7.3e-169 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
CNHFAHCC_03303 | 2.9e-309 | bshC | S | Involved in bacillithiol (BSH) biosynthesis. May catalyze the last step of the pathway, the addition of cysteine to glucosamine malate (GlcN-Mal) to generate BSH | ||
CNHFAHCC_03304 | 2.9e-78 | mraZ | K | Belongs to the MraZ family | ||
CNHFAHCC_03305 | 6.6e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
CNHFAHCC_03306 | 3.7e-44 | ftsL | D | Essential cell division protein | ||
CNHFAHCC_03307 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
CNHFAHCC_03308 | 0.0 | ftsI | 3.4.16.4 | M | stage V sporulation protein D | |
CNHFAHCC_03309 | 5.2e-281 | murE | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
CNHFAHCC_03310 | 3.2e-170 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
CNHFAHCC_03311 | 2.6e-255 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
CNHFAHCC_03312 | 1.9e-198 | spoVE | D | Belongs to the SEDS family | ||
CNHFAHCC_03313 | 2.3e-201 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
CNHFAHCC_03314 | 5.3e-167 | murB | 1.3.1.98 | M | cell wall formation | |
CNHFAHCC_03315 | 2.6e-138 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
CNHFAHCC_03316 | 2.4e-103 | ylxW | S | protein conserved in bacteria | ||
CNHFAHCC_03317 | 2.8e-117 | ylxX | S | protein conserved in bacteria | ||
CNHFAHCC_03318 | 6.2e-58 | sbp | S | small basic protein | ||
CNHFAHCC_03319 | 2.4e-229 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
CNHFAHCC_03320 | 2e-203 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
CNHFAHCC_03321 | 0.0 | bpr | O | COG1404 Subtilisin-like serine proteases | ||
CNHFAHCC_03322 | 4.4e-172 | spoIIGA | M | aspartic protease that is responsible for the proteolytic cleavage of the RNA polymerase sigma E factor (SigE spoIIGB) to yield the active peptide in the mother cell during sporulation. Responds to a signal from the forespore that is triggered by the extracellular signal protein SpoIIR | ||
CNHFAHCC_03323 | 1.4e-125 | sigE | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_03324 | 3.6e-140 | sigG | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_03325 | 1.1e-147 | modF | 3.6.3.21, 3.6.3.34 | P | COG1119 ABC-type molybdenum transport system, ATPase component photorepair protein PhrA | |
CNHFAHCC_03326 | 1.3e-256 | argE | 3.5.1.16 | E | Acetylornithine deacetylase | |
CNHFAHCC_03327 | 2.4e-37 | ylmC | S | sporulation protein | ||
CNHFAHCC_03328 | 1.1e-158 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
CNHFAHCC_03329 | 2.9e-125 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
CNHFAHCC_03330 | 1.4e-62 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
CNHFAHCC_03331 | 1.3e-39 | yggT | S | membrane | ||
CNHFAHCC_03332 | 6.7e-139 | ylmH | 5.4.99.23, 5.4.99.24 | S | conserved protein, contains S4-like domain | |
CNHFAHCC_03333 | 2.6e-67 | divIVA | D | Cell division initiation protein | ||
CNHFAHCC_03334 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
CNHFAHCC_03335 | 1.3e-63 | dksA | T | COG1734 DnaK suppressor protein | ||
CNHFAHCC_03336 | 1.8e-78 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
CNHFAHCC_03337 | 1.1e-164 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
CNHFAHCC_03338 | 2.7e-94 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
CNHFAHCC_03339 | 9e-232 | pyrP | F | Xanthine uracil | ||
CNHFAHCC_03340 | 1.4e-167 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
CNHFAHCC_03341 | 1.7e-251 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
CNHFAHCC_03342 | 5e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
CNHFAHCC_03343 | 0.0 | carB | 6.3.5.5 | F | Belongs to the CarB family | |
CNHFAHCC_03344 | 4.8e-145 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
CNHFAHCC_03345 | 2.9e-176 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
CNHFAHCC_03346 | 8e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
CNHFAHCC_03347 | 2.9e-116 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
CNHFAHCC_03348 | 3.5e-142 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
CNHFAHCC_03349 | 1.1e-179 | cysP | P | phosphate transporter | ||
CNHFAHCC_03350 | 1.3e-223 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
CNHFAHCC_03351 | 7.3e-109 | cysC | 2.7.1.25 | P | Catalyzes the synthesis of activated sulfate | |
CNHFAHCC_03352 | 2.2e-145 | hemD | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
CNHFAHCC_03353 | 2e-146 | cbiX | 4.99.1.3, 4.99.1.4, 5.4.99.60, 5.4.99.61 | S | Sirohydrochlorin ferrochelatase | |
CNHFAHCC_03354 | 4.3e-83 | cysG | 1.3.1.76, 4.99.1.4 | H | Siroheme synthase | |
CNHFAHCC_03355 | 0.0 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
CNHFAHCC_03356 | 0.0 | yloB | 3.6.3.8 | P | COG0474 Cation transport ATPase | |
CNHFAHCC_03357 | 2.8e-154 | yloC | S | stress-induced protein | ||
CNHFAHCC_03358 | 1.5e-40 | ylzA | S | Belongs to the UPF0296 family | ||
CNHFAHCC_03359 | 3.1e-110 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
CNHFAHCC_03360 | 2.2e-28 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
CNHFAHCC_03361 | 8.8e-226 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
CNHFAHCC_03362 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
CNHFAHCC_03363 | 6e-85 | def | 2.1.2.9, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
CNHFAHCC_03364 | 3.8e-176 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
CNHFAHCC_03365 | 2.9e-254 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
CNHFAHCC_03366 | 4.8e-207 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
CNHFAHCC_03367 | 2.4e-141 | stp | 3.1.3.16 | T | phosphatase | |
CNHFAHCC_03368 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
CNHFAHCC_03369 | 8.6e-170 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
CNHFAHCC_03370 | 4.2e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
CNHFAHCC_03371 | 3.1e-121 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
CNHFAHCC_03372 | 4.2e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
CNHFAHCC_03373 | 5.5e-59 | asp | S | protein conserved in bacteria | ||
CNHFAHCC_03374 | 2.7e-302 | yloV | S | kinase related to dihydroxyacetone kinase | ||
CNHFAHCC_03375 | 1.9e-118 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
CNHFAHCC_03376 | 9.3e-156 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
CNHFAHCC_03377 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
CNHFAHCC_03378 | 4e-80 | fapR | 5.3.1.23 | K | Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism | |
CNHFAHCC_03379 | 4.3e-178 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
CNHFAHCC_03380 | 9.1e-170 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
CNHFAHCC_03381 | 6.1e-129 | IQ | reductase | |||
CNHFAHCC_03382 | 2.8e-32 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
CNHFAHCC_03383 | 1.2e-135 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
CNHFAHCC_03384 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
CNHFAHCC_03385 | 8.8e-176 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
CNHFAHCC_03386 | 2.9e-87 | |||||
CNHFAHCC_03387 | 1.6e-49 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
CNHFAHCC_03388 | 6e-236 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
CNHFAHCC_03389 | 1.1e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
CNHFAHCC_03390 | 1.2e-36 | ylqC | S | Belongs to the UPF0109 family | ||
CNHFAHCC_03391 | 1.3e-61 | ylqD | S | YlqD protein | ||
CNHFAHCC_03392 | 5.3e-95 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
CNHFAHCC_03393 | 9.2e-138 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
CNHFAHCC_03394 | 1.4e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
CNHFAHCC_03395 | 4.2e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
CNHFAHCC_03396 | 4.1e-136 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CNHFAHCC_03397 | 8.5e-291 | ylqG | ||||
CNHFAHCC_03398 | 3e-44 | ylqH | S | homolog of the cytoplasmic domain of flagellar protein FhlB | ||
CNHFAHCC_03399 | 3.4e-211 | sucC | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
CNHFAHCC_03400 | 1.1e-167 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
CNHFAHCC_03401 | 1.7e-170 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
CNHFAHCC_03402 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
CNHFAHCC_03403 | 7.4e-247 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
CNHFAHCC_03404 | 2.5e-169 | xerC | L | tyrosine recombinase XerC | ||
CNHFAHCC_03405 | 4.4e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
CNHFAHCC_03406 | 1.5e-250 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
CNHFAHCC_03407 | 9.2e-136 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
CNHFAHCC_03408 | 2.3e-63 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
CNHFAHCC_03409 | 6.9e-75 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
CNHFAHCC_03410 | 3.5e-28 | fliE | N | Flagellar hook-basal body | ||
CNHFAHCC_03411 | 2.4e-255 | fliF | N | The M ring may be actively involved in energy transduction | ||
CNHFAHCC_03412 | 2e-178 | fliG | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
CNHFAHCC_03413 | 2.5e-106 | fliH | NU | COG1317 Flagellar biosynthesis type III secretory pathway protein | ||
CNHFAHCC_03414 | 2.5e-242 | fliI | 3.6.3.14 | NU | COG1157 Flagellar biosynthesis type III secretory pathway ATPase | |
CNHFAHCC_03415 | 1.5e-69 | fliJ | N | Flagellar biosynthesis chaperone | ||
CNHFAHCC_03416 | 7.7e-37 | ylxF | S | MgtE intracellular N domain | ||
CNHFAHCC_03417 | 1.2e-221 | fliK | N | Flagellar hook-length control protein | ||
CNHFAHCC_03418 | 1.7e-72 | flgD | N | Flagellar basal body rod modification protein | ||
CNHFAHCC_03419 | 8.2e-140 | flgG | N | Flagellar basal body rod | ||
CNHFAHCC_03420 | 2.6e-32 | flbD | N | protein, possibly involved in motility | ||
CNHFAHCC_03421 | 4.6e-49 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
CNHFAHCC_03422 | 1.9e-181 | fliM | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
CNHFAHCC_03423 | 4.5e-184 | fliN | N | FliN is one of three proteins (FliG, FliN, FliM) that form the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
CNHFAHCC_03424 | 1.6e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | response regulator | |
CNHFAHCC_03425 | 9.3e-97 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
CNHFAHCC_03426 | 1.6e-109 | fliP | N | Plays a role in the flagellum-specific transport system | ||
CNHFAHCC_03427 | 2.3e-36 | fliQ | N | Role in flagellar biosynthesis | ||
CNHFAHCC_03428 | 3.6e-132 | fliR | N | Flagellar biosynthetic protein FliR | ||
CNHFAHCC_03429 | 1.4e-190 | flhB | N | Required for formation of the rod structure in the basal body of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
CNHFAHCC_03430 | 0.0 | flhA | N | Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
CNHFAHCC_03431 | 6.4e-196 | flhF | N | Flagellar biosynthesis regulator FlhF | ||
CNHFAHCC_03432 | 7.5e-158 | flhG | D | Belongs to the ParA family | ||
CNHFAHCC_03433 | 5.8e-197 | cheB | 3.1.1.61, 3.5.1.44 | NT | catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR | |
CNHFAHCC_03434 | 0.0 | cheA | 2.7.13.3 | NT | COG0643 Chemotaxis protein histidine kinase and related kinases | |
CNHFAHCC_03435 | 2.8e-79 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
CNHFAHCC_03436 | 1.3e-111 | cheC | NT | COG1776 Chemotaxis protein CheC, inhibitor of MCP methylation | ||
CNHFAHCC_03437 | 1.1e-86 | cheD | 3.5.1.44 | NT | Deamidates glutamine residues to glutamate on methyl- accepting chemotaxis receptors (MCPs). CheD-mediated MCP deamidation is required for productive communication of the conformational signals of the chemoreceptors to the CheA kinase | |
CNHFAHCC_03438 | 5.6e-138 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_03439 | 4.3e-78 | ylxL | ||||
CNHFAHCC_03440 | 1e-131 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
CNHFAHCC_03441 | 6.3e-157 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
CNHFAHCC_03442 | 2.7e-126 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
CNHFAHCC_03443 | 6.4e-91 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
CNHFAHCC_03444 | 8.3e-145 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
CNHFAHCC_03445 | 1.2e-138 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
CNHFAHCC_03446 | 4.6e-216 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
CNHFAHCC_03447 | 7.7e-233 | rasP | M | zinc metalloprotease | ||
CNHFAHCC_03448 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
CNHFAHCC_03449 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
CNHFAHCC_03450 | 3.3e-80 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
CNHFAHCC_03451 | 1.1e-203 | nusA | K | Participates in both transcription termination and antitermination | ||
CNHFAHCC_03452 | 3.4e-32 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
CNHFAHCC_03453 | 3.1e-47 | ylxQ | J | ribosomal protein | ||
CNHFAHCC_03454 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
CNHFAHCC_03455 | 3e-44 | ylxP | S | protein conserved in bacteria | ||
CNHFAHCC_03456 | 2.5e-56 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
CNHFAHCC_03457 | 1.3e-173 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
CNHFAHCC_03458 | 1.1e-169 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
CNHFAHCC_03459 | 6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
CNHFAHCC_03460 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
CNHFAHCC_03461 | 4.2e-183 | ylxY | 3.5.1.104 | G | Sporulation protein, polysaccharide deacetylase | |
CNHFAHCC_03462 | 4.4e-233 | pepR | S | Belongs to the peptidase M16 family | ||
CNHFAHCC_03463 | 2.6e-42 | ymxH | S | YlmC YmxH family | ||
CNHFAHCC_03464 | 2.9e-162 | spoVFA | 1.1.1.29, 1.1.1.399, 1.1.1.95 | CH | Dipicolinate synthase subunit A | |
CNHFAHCC_03465 | 4.3e-109 | spoVFB | H | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) | ||
CNHFAHCC_03466 | 1.4e-192 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
CNHFAHCC_03467 | 3.8e-221 | dapG | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
CNHFAHCC_03468 | 1.4e-156 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
CNHFAHCC_03469 | 1.9e-308 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
CNHFAHCC_03470 | 5.3e-133 | tepA | 3.4.21.92 | OU | COG0740 Protease subunit of ATP-dependent Clp proteases | |
CNHFAHCC_03471 | 4.4e-32 | S | YlzJ-like protein | |||
CNHFAHCC_03472 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
CNHFAHCC_03473 | 1.4e-133 | ymfC | K | Transcriptional regulator | ||
CNHFAHCC_03474 | 9.2e-207 | ymfD | EGP | Major facilitator Superfamily | ||
CNHFAHCC_03475 | 2.6e-236 | ymfF | S | Peptidase M16 | ||
CNHFAHCC_03476 | 1.4e-242 | ymfH | S | zinc protease | ||
CNHFAHCC_03477 | 9.2e-130 | ymfI | 1.1.1.100, 1.3.1.28 | S | Catalyzes the first of the two reduction steps in the elongation cycle of fatty acid synthesis | |
CNHFAHCC_03478 | 4.8e-41 | ymfJ | S | Protein of unknown function (DUF3243) | ||
CNHFAHCC_03479 | 2.2e-80 | ymfK | S | Protein of unknown function (DUF3388) | ||
CNHFAHCC_03480 | 3.1e-53 | ymfK | S | Protein of unknown function (DUF3388) | ||
CNHFAHCC_03481 | 1.9e-124 | ymfM | S | protein conserved in bacteria | ||
CNHFAHCC_03482 | 2.5e-101 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
CNHFAHCC_03483 | 1.9e-236 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
CNHFAHCC_03484 | 8.1e-188 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
CNHFAHCC_03485 | 1e-215 | pbpX | V | Beta-lactamase | ||
CNHFAHCC_03486 | 2.1e-224 | rny | S | Endoribonuclease that initiates mRNA decay | ||
CNHFAHCC_03487 | 1.9e-152 | ymdB | S | protein conserved in bacteria | ||
CNHFAHCC_03488 | 1.2e-36 | spoVS | S | Stage V sporulation protein S | ||
CNHFAHCC_03489 | 2.7e-199 | tdh | 1.1.1.103 | C | Catalyzes the NAD( )-dependent oxidation of L-threonine to 2-amino-3-ketobutyrate | |
CNHFAHCC_03490 | 6.5e-218 | kbl | 2.3.1.29, 2.3.1.47 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
CNHFAHCC_03491 | 2.7e-296 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
CNHFAHCC_03492 | 9.2e-69 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
CNHFAHCC_03493 | 2.2e-88 | cotE | S | Spore coat protein | ||
CNHFAHCC_03494 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
CNHFAHCC_03495 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
CNHFAHCC_03496 | 2.3e-70 | S | Regulatory protein YrvL | |||
CNHFAHCC_03498 | 1.2e-97 | ymcC | S | Membrane | ||
CNHFAHCC_03499 | 4.4e-109 | pksA | K | Transcriptional regulator | ||
CNHFAHCC_03500 | 2.5e-129 | pksB | 3.1.2.6 | S | Polyketide biosynthesis | |
CNHFAHCC_03502 | 2.6e-163 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
CNHFAHCC_03503 | 2.4e-186 | pksD | Q | Acyl transferase domain | ||
CNHFAHCC_03504 | 0.0 | fabD | 1.13.12.16, 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
CNHFAHCC_03505 | 1.4e-37 | acpK | IQ | Phosphopantetheine attachment site | ||
CNHFAHCC_03506 | 2.7e-238 | pksF | 2.3.1.179, 2.3.1.41 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
CNHFAHCC_03507 | 1.3e-245 | pksG | 2.3.3.10 | I | synthase | |
CNHFAHCC_03508 | 2.6e-143 | pksH | 4.2.1.18 | I | enoyl-CoA hydratase | |
CNHFAHCC_03509 | 2.7e-137 | pksI | I | Belongs to the enoyl-CoA hydratase isomerase family | ||
CNHFAHCC_03510 | 0.0 | rhiB | IQ | polyketide synthase | ||
CNHFAHCC_03511 | 0.0 | pfaA | Q | Polyketide synthase of type I | ||
CNHFAHCC_03512 | 0.0 | pfaA | 4.1.1.35 | GT4 | IQ | polyketide synthase |
CNHFAHCC_03513 | 0.0 | dhbF | IQ | polyketide synthase | ||
CNHFAHCC_03514 | 0.0 | dhbF | IQ | polyketide synthase | ||
CNHFAHCC_03515 | 0.0 | pks13 | HQ | Beta-ketoacyl synthase | ||
CNHFAHCC_03516 | 2.5e-233 | cypA | C | Cytochrome P450 | ||
CNHFAHCC_03517 | 1.2e-61 | ymzB | ||||
CNHFAHCC_03518 | 6.6e-164 | ymaE | S | Metallo-beta-lactamase superfamily | ||
CNHFAHCC_03519 | 4.6e-252 | aprX | O | Belongs to the peptidase S8 family | ||
CNHFAHCC_03520 | 2.1e-126 | ymaC | S | Replication protein | ||
CNHFAHCC_03521 | 5.4e-80 | ymaD | O | redox protein, regulator of disulfide bond formation | ||
CNHFAHCC_03522 | 4.7e-55 | ebrB | P | COG2076 Membrane transporters of cations and cationic drugs | ||
CNHFAHCC_03523 | 4.9e-51 | ebrA | P | Small Multidrug Resistance protein | ||
CNHFAHCC_03525 | 4.8e-47 | ymaF | S | YmaF family | ||
CNHFAHCC_03526 | 9.3e-175 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
CNHFAHCC_03527 | 1.9e-33 | hfq | J | RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs | ||
CNHFAHCC_03528 | 6.3e-23 | |||||
CNHFAHCC_03529 | 7.2e-22 | ymzA | ||||
CNHFAHCC_03530 | 1.9e-49 | nrdI | 1.17.4.1 | F | Probably involved in ribonucleotide reductase function | |
CNHFAHCC_03531 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
CNHFAHCC_03532 | 4.5e-188 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
CNHFAHCC_03533 | 2e-109 | ymaB | ||||
CNHFAHCC_03534 | 8e-116 | cwlC | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
CNHFAHCC_03536 | 1.7e-176 | spoVK | O | stage V sporulation protein K | ||
CNHFAHCC_03537 | 5.5e-231 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
CNHFAHCC_03538 | 3.3e-244 | ynbB | 4.4.1.1 | P | COG4100 Cystathionine beta-lyase family protein involved in aluminum resistance | |
CNHFAHCC_03539 | 1.1e-68 | glnR | K | transcriptional | ||
CNHFAHCC_03540 | 7e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
CNHFAHCC_03541 | 5e-10 | |||||
CNHFAHCC_03542 | 2.5e-32 | |||||
CNHFAHCC_03543 | 5.8e-39 | |||||
CNHFAHCC_03544 | 6.8e-80 | G | regulation of fungal-type cell wall biogenesis | |||
CNHFAHCC_03545 | 4.9e-145 | ynaC | ||||
CNHFAHCC_03546 | 2e-99 | ynaD | J | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_03547 | 1.9e-123 | ynaE | S | Domain of unknown function (DUF3885) | ||
CNHFAHCC_03548 | 6.4e-60 | ynaF | ||||
CNHFAHCC_03551 | 1.1e-83 | XK27_05370 | 5.3.1.24 | E | phosphoribosylanthranilate isomerase activity | |
CNHFAHCC_03552 | 2.7e-255 | xynT | G | MFS/sugar transport protein | ||
CNHFAHCC_03553 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
CNHFAHCC_03554 | 1e-215 | xylR | GK | ROK family | ||
CNHFAHCC_03555 | 4e-264 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
CNHFAHCC_03556 | 6e-293 | xylB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | xylulose kinase | |
CNHFAHCC_03557 | 1.4e-113 | yokF | 3.1.31.1 | L | RNA catabolic process | |
CNHFAHCC_03558 | 3.5e-247 | iolT | EGP | Major facilitator Superfamily | ||
CNHFAHCC_03559 | 2.7e-219 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
CNHFAHCC_03560 | 6.3e-84 | yncE | S | Protein of unknown function (DUF2691) | ||
CNHFAHCC_03561 | 4.9e-78 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | Deoxyuridine 5'-triphosphate | |
CNHFAHCC_03562 | 5.2e-15 | |||||
CNHFAHCC_03566 | 1.2e-165 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
CNHFAHCC_03568 | 1.3e-134 | S | Domain of unknown function, YrpD | |||
CNHFAHCC_03571 | 7.9e-25 | tatA | U | protein secretion | ||
CNHFAHCC_03572 | 1.8e-71 | |||||
CNHFAHCC_03573 | 5.2e-80 | yndB | S | Activator of Hsp90 ATPase homolog 1-like protein | ||
CNHFAHCC_03576 | 5.7e-286 | gerAA | EG | Spore germination protein | ||
CNHFAHCC_03577 | 4.5e-197 | gerAB | U | Spore germination | ||
CNHFAHCC_03578 | 4.2e-220 | gerLC | S | Spore germination protein | ||
CNHFAHCC_03579 | 7.7e-154 | yndG | S | DoxX-like family | ||
CNHFAHCC_03580 | 2.1e-117 | yndH | S | Domain of unknown function (DUF4166) | ||
CNHFAHCC_03581 | 0.0 | yndJ | S | YndJ-like protein | ||
CNHFAHCC_03583 | 8.6e-139 | yndL | S | Replication protein | ||
CNHFAHCC_03584 | 1.5e-92 | yndM | S | Protein of unknown function (DUF2512) | ||
CNHFAHCC_03585 | 2e-79 | fosB | 2.5.1.18 | H | Metallothiol transferase which confers resistance to fosfomycin by catalyzing the addition of a thiol cofactor to fosfomycin. L-cysteine is probably the physiological thiol donor | |
CNHFAHCC_03587 | 2.6e-109 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
CNHFAHCC_03588 | 3.4e-49 | yneA | D | Inhibits cell division during the SOS response. Affects a later stage of the cell division protein assembly, after the assembly of the Z ring, by probably suppressing recruitment of FtsL and or DivIC to the division machinery | ||
CNHFAHCC_03589 | 9.2e-113 | yneB | L | resolvase | ||
CNHFAHCC_03590 | 1.3e-32 | ynzC | S | UPF0291 protein | ||
CNHFAHCC_03591 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
CNHFAHCC_03592 | 2.2e-81 | yneE | S | Sporulation inhibitor of replication protein sirA | ||
CNHFAHCC_03593 | 1.8e-28 | yneF | S | UPF0154 protein | ||
CNHFAHCC_03594 | 6.4e-14 | ynzD | S | Spo0E like sporulation regulatory protein | ||
CNHFAHCC_03595 | 7.1e-127 | ccdA | O | cytochrome c biogenesis protein | ||
CNHFAHCC_03596 | 7.2e-59 | cheB | 3.1.1.61, 3.5.1.44 | T | cheY-homologous receiver domain | |
CNHFAHCC_03597 | 5.1e-76 | yneJ | O | COG4846 Membrane protein involved in cytochrome C biogenesis | ||
CNHFAHCC_03598 | 4.2e-74 | yneK | S | Protein of unknown function (DUF2621) | ||
CNHFAHCC_03599 | 4.1e-65 | hspX | O | Spore coat protein | ||
CNHFAHCC_03600 | 3.9e-19 | sspP | S | Belongs to the SspP family | ||
CNHFAHCC_03601 | 2.2e-14 | sspO | S | Belongs to the SspO family | ||
CNHFAHCC_03602 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
CNHFAHCC_03603 | 4.1e-92 | yneN | CO | alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | ||
CNHFAHCC_03604 | 3.1e-08 | sspN | S | Small acid-soluble spore protein N family | ||
CNHFAHCC_03605 | 3.9e-35 | tlp | S | Belongs to the Tlp family | ||
CNHFAHCC_03606 | 1.2e-73 | yneP | S | Thioesterase-like superfamily | ||
CNHFAHCC_03607 | 1.3e-53 | yneQ | ||||
CNHFAHCC_03608 | 4.1e-49 | yneR | S | Belongs to the HesB IscA family | ||
CNHFAHCC_03609 | 5e-94 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
CNHFAHCC_03610 | 6.6e-69 | yccU | S | CoA-binding protein | ||
CNHFAHCC_03611 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
CNHFAHCC_03612 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
CNHFAHCC_03613 | 2.3e-12 | |||||
CNHFAHCC_03614 | 1.6e-70 | ynfC | ||||
CNHFAHCC_03615 | 8.2e-252 | agcS | E | Sodium alanine symporter | ||
CNHFAHCC_03616 | 1.1e-286 | bglC5 | 3.2.1.4 | GH5,GH9 | G | PFAM glycoside hydrolase family 5 |
CNHFAHCC_03618 | 3.7e-251 | xynC | 3.2.1.136 | GH5 | M | Belongs to the glycosyl hydrolase 30 family |
CNHFAHCC_03619 | 4.4e-299 | xynD3 | 3.2.1.55 | CBM6,GH43 | G | Belongs to the glycosyl hydrolase 43 family |
CNHFAHCC_03620 | 2.4e-80 | yngA | S | membrane | ||
CNHFAHCC_03621 | 4.1e-164 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
CNHFAHCC_03622 | 5.5e-104 | yngC | S | membrane-associated protein | ||
CNHFAHCC_03623 | 1.9e-233 | nrnB | S | phosphohydrolase (DHH superfamily) | ||
CNHFAHCC_03624 | 6.3e-290 | yngE | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
CNHFAHCC_03625 | 2.2e-137 | yngF | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
CNHFAHCC_03626 | 8e-168 | mvaB | 4.1.3.4, 6.4.1.4 | E | Hydroxymethylglutaryl-CoA lyase | |
CNHFAHCC_03627 | 6e-32 | pycB | 2.3.1.12, 6.4.1.1 | I | Biotin carboxyl carrier protein | |
CNHFAHCC_03628 | 3e-251 | yngH | 6.3.4.14, 6.4.1.2, 6.4.1.3, 6.4.1.4 | I | Biotin carboxylase | |
CNHFAHCC_03629 | 0.0 | yngI | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
CNHFAHCC_03630 | 4.4e-211 | yngJ | 1.3.8.1, 1.3.99.12 | I | acyl-CoA dehydrogenase | |
CNHFAHCC_03631 | 1.8e-31 | S | Family of unknown function (DUF5367) | |||
CNHFAHCC_03633 | 1.3e-306 | yngK | T | Glycosyl hydrolase-like 10 | ||
CNHFAHCC_03634 | 2.8e-64 | yngL | S | Protein of unknown function (DUF1360) | ||
CNHFAHCC_03635 | 0.0 | 6.3.2.14 | Q | amino acid activation for nonribosomal peptide biosynthetic process | ||
CNHFAHCC_03636 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
CNHFAHCC_03637 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
CNHFAHCC_03638 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
CNHFAHCC_03639 | 4.3e-275 | dacC | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
CNHFAHCC_03640 | 6e-193 | yoxA | 5.1.3.3 | G | Aldose 1-epimerase | |
CNHFAHCC_03641 | 2.3e-246 | yoeA | V | MATE efflux family protein | ||
CNHFAHCC_03642 | 1.1e-98 | yoeB | S | IseA DL-endopeptidase inhibitor | ||
CNHFAHCC_03644 | 2.2e-96 | L | Integrase | |||
CNHFAHCC_03645 | 3e-34 | yoeD | G | Helix-turn-helix domain | ||
CNHFAHCC_03646 | 0.0 | ggt | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
CNHFAHCC_03647 | 2.5e-158 | gltR1 | K | Transcriptional regulator | ||
CNHFAHCC_03648 | 5e-187 | yogA | C | COG0604 NADPH quinone reductase and related Zn-dependent oxidoreductases | ||
CNHFAHCC_03649 | 2.7e-293 | gltD | 1.4.1.13, 1.4.1.14 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
CNHFAHCC_03650 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase | |
CNHFAHCC_03651 | 7.8e-155 | gltC | K | Transcriptional regulator | ||
CNHFAHCC_03652 | 4.1e-206 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
CNHFAHCC_03653 | 2.5e-144 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
CNHFAHCC_03654 | 1.9e-59 | rtp | K | Plays a role in DNA replication and termination (fork arrest mechanism). Two dimers of rtp bind to the two inverted repeat regions (IRI and IRII) present in the termination site. The binding of each dimer is centered on an 8 bp direct repeat | ||
CNHFAHCC_03655 | 2.2e-123 | fabG | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
CNHFAHCC_03656 | 3e-42 | yoxC | S | Bacterial protein of unknown function (DUF948) | ||
CNHFAHCC_03657 | 3.1e-144 | yoxB | ||||
CNHFAHCC_03658 | 7.5e-97 | yoaA | 2.3.1.128 | J | COG1670 Acetyltransferases, including N-acetylases of ribosomal proteins | |
CNHFAHCC_03659 | 6.2e-235 | yoaB | EGP | Major facilitator Superfamily | ||
CNHFAHCC_03660 | 1e-284 | yoaC | 2.7.1.12, 2.7.1.17, 2.7.1.189, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
CNHFAHCC_03661 | 1.7e-190 | yoaD | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
CNHFAHCC_03662 | 0.0 | yoaE | C | belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
CNHFAHCC_03663 | 1.9e-33 | yoaF | ||||
CNHFAHCC_03664 | 2.2e-08 | ywlA | S | Uncharacterised protein family (UPF0715) | ||
CNHFAHCC_03665 | 7e-14 | |||||
CNHFAHCC_03666 | 1.5e-38 | S | Protein of unknown function (DUF4025) | |||
CNHFAHCC_03667 | 7e-66 | mcpU | NT | methyl-accepting chemotaxis protein | ||
CNHFAHCC_03668 | 1.6e-116 | mcpU | NT | methyl-accepting chemotaxis protein | ||
CNHFAHCC_03669 | 8.7e-281 | hpaB | 1.14.14.9 | Q | COG2368 Aromatic ring hydroxylase | |
CNHFAHCC_03670 | 3.8e-133 | yoaJ | G | Endoglucanase C-terminal domain subunit and related proteins | ||
CNHFAHCC_03671 | 2.3e-111 | yoaK | S | Membrane | ||
CNHFAHCC_03672 | 2.3e-198 | pelB | 4.2.2.10, 4.2.2.2 | G | Amb_all | |
CNHFAHCC_03673 | 1.1e-132 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
CNHFAHCC_03675 | 2.6e-235 | oxdC | 4.1.1.2 | G | Oxalate decarboxylase | |
CNHFAHCC_03677 | 1.5e-146 | yoaP | 3.1.3.18 | K | YoaP-like | |
CNHFAHCC_03678 | 9.8e-67 | yoaQ | S | Evidence 4 Homologs of previously reported genes of | ||
CNHFAHCC_03679 | 4.1e-89 | |||||
CNHFAHCC_03680 | 2.4e-172 | yoaR | V | vancomycin resistance protein | ||
CNHFAHCC_03681 | 4.3e-75 | yoaS | S | Protein of unknown function (DUF2975) | ||
CNHFAHCC_03682 | 4.2e-37 | yozG | K | Transcriptional regulator | ||
CNHFAHCC_03683 | 1.1e-149 | yoaT | S | Protein of unknown function (DUF817) | ||
CNHFAHCC_03684 | 8.6e-159 | yoaU | K | LysR substrate binding domain | ||
CNHFAHCC_03685 | 6e-160 | yijE | EG | EamA-like transporter family | ||
CNHFAHCC_03686 | 3.7e-78 | yoaW | ||||
CNHFAHCC_03687 | 1.1e-118 | yoaZ | 1.11.1.6, 3.5.1.124 | S | DJ-1/PfpI family | |
CNHFAHCC_03688 | 2.3e-170 | bla | 3.5.2.6 | V | beta-lactamase | |
CNHFAHCC_03693 | 0.0 | pps | 2.7.9.2 | GT | phosphoenolpyruvate synthase | |
CNHFAHCC_03694 | 1.8e-121 | xlnB | 3.2.1.8 | G | Glycosyl hydrolases family 11 | |
CNHFAHCC_03696 | 1.4e-37 | S | TM2 domain | |||
CNHFAHCC_03697 | 5.7e-58 | K | Helix-turn-helix | |||
CNHFAHCC_03699 | 1.6e-69 | yoaQ | S | Evidence 4 Homologs of previously reported genes of | ||
CNHFAHCC_03700 | 6.6e-127 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
CNHFAHCC_03701 | 1.8e-178 | yobF | ||||
CNHFAHCC_03706 | 1.7e-207 | S | aspartate phosphatase | |||
CNHFAHCC_03708 | 3.1e-80 | dinB2 | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
CNHFAHCC_03709 | 1.4e-59 | dinB2 | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
CNHFAHCC_03710 | 2.6e-38 | S | YolD-like protein | |||
CNHFAHCC_03711 | 1.2e-49 | |||||
CNHFAHCC_03712 | 0.0 | K | Psort location Cytoplasmic, score | |||
CNHFAHCC_03714 | 2.7e-157 | yobJ | ||||
CNHFAHCC_03715 | 3e-86 | S | SMI1-KNR4 cell-wall | |||
CNHFAHCC_03716 | 0.0 | L | A nuclease of the HNH/ENDO VII superfamily with conserved LHH | |||
CNHFAHCC_03717 | 7.9e-105 | yokH | G | SMI1 / KNR4 family | ||
CNHFAHCC_03718 | 5.2e-278 | iaaM | 1.4.3.4 | E | COG1231 Monoamine oxidase | |
CNHFAHCC_03719 | 0.0 | yobO | M | Pectate lyase superfamily protein | ||
CNHFAHCC_03720 | 9.9e-55 | csaA | 6.1.1.10, 6.1.1.20, 6.1.1.6 | J | tRNA-binding protein | |
CNHFAHCC_03721 | 2.7e-137 | yobQ | K | helix_turn_helix, arabinose operon control protein | ||
CNHFAHCC_03722 | 2.5e-143 | yobR | 2.3.1.1 | J | FR47-like protein | |
CNHFAHCC_03723 | 3e-99 | yobS | K | Transcriptional regulator | ||
CNHFAHCC_03724 | 4.2e-132 | yobT | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
CNHFAHCC_03725 | 1.5e-88 | yobU | K | Bacterial transcription activator, effector binding domain | ||
CNHFAHCC_03726 | 9e-178 | yobV | K | WYL domain | ||
CNHFAHCC_03727 | 2.5e-95 | yobW | ||||
CNHFAHCC_03728 | 1e-51 | czrA | K | transcriptional | ||
CNHFAHCC_03729 | 4.4e-118 | pvaA | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
CNHFAHCC_03730 | 1.5e-92 | yozB | S | membrane | ||
CNHFAHCC_03731 | 2.2e-145 | |||||
CNHFAHCC_03732 | 1.9e-94 | yocC | ||||
CNHFAHCC_03733 | 6.9e-189 | yocD | 3.4.17.13 | V | peptidase S66 | |
CNHFAHCC_03734 | 4.1e-203 | des | 1.14.19.23, 1.14.19.45 | I | fatty acid desaturase | |
CNHFAHCC_03735 | 3.2e-198 | desK | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_03736 | 1e-105 | desR | T | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_03737 | 7.1e-113 | yocH | CBM50 | M | COG1388 FOG LysM repeat | |
CNHFAHCC_03738 | 0.0 | recQ | 3.6.4.12 | L | DNA helicase | |
CNHFAHCC_03739 | 7.9e-114 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
CNHFAHCC_03740 | 3.3e-83 | dksA | T | general stress protein | ||
CNHFAHCC_03741 | 6.4e-54 | yocL | ||||
CNHFAHCC_03742 | 6.6e-34 | |||||
CNHFAHCC_03743 | 1.3e-87 | yocM | O | Belongs to the small heat shock protein (HSP20) family | ||
CNHFAHCC_03744 | 1.1e-40 | yozN | ||||
CNHFAHCC_03745 | 1.9e-36 | yocN | ||||
CNHFAHCC_03746 | 4.2e-56 | yozO | S | Bacterial PH domain | ||
CNHFAHCC_03747 | 2.7e-31 | yozC | ||||
CNHFAHCC_03748 | 4e-289 | dhaS | 1.2.1.3, 1.2.1.39 | C | Belongs to the aldehyde dehydrogenase family | |
CNHFAHCC_03749 | 0.0 | sqhC | 4.2.1.137, 5.4.99.7 | I | COG1657 Squalene cyclase | |
CNHFAHCC_03750 | 5.4e-166 | sodA | 1.15.1.1 | P | Superoxide dismutase | |
CNHFAHCC_03751 | 3.4e-231 | yocR | S | Belongs to the sodium neurotransmitter symporter (SNF) (TC 2.A.22) family | ||
CNHFAHCC_03752 | 5.1e-168 | yocS | S | -transporter | ||
CNHFAHCC_03753 | 1.8e-194 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
CNHFAHCC_03754 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components 2- oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) | |
CNHFAHCC_03755 | 0.0 | yojO | P | Von Willebrand factor | ||
CNHFAHCC_03756 | 1.1e-161 | yojN | S | ATPase family associated with various cellular activities (AAA) | ||
CNHFAHCC_03757 | 1e-110 | sodC | 1.15.1.1 | P | Destroys radicals which are normally produced within the cells and which are toxic to biological systems | |
CNHFAHCC_03758 | 1.6e-198 | sle1 | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
CNHFAHCC_03759 | 1.8e-231 | yojK | CG | UDP-glucoronosyl and UDP-glucosyl transferase | ||
CNHFAHCC_03760 | 1.2e-109 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
CNHFAHCC_03762 | 4.2e-245 | norM | V | Multidrug efflux pump | ||
CNHFAHCC_03763 | 8.4e-151 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
CNHFAHCC_03764 | 2.1e-125 | yojG | S | deacetylase | ||
CNHFAHCC_03765 | 2.2e-60 | yojF | S | Protein of unknown function (DUF1806) | ||
CNHFAHCC_03766 | 1.5e-43 | |||||
CNHFAHCC_03767 | 3.5e-163 | rarD | S | -transporter | ||
CNHFAHCC_03768 | 2.6e-61 | yozR | S | COG0071 Molecular chaperone (small heat shock protein) | ||
CNHFAHCC_03769 | 3.4e-09 | |||||
CNHFAHCC_03770 | 8.2e-209 | gntP | EG | COG2610 H gluconate symporter and related permeases | ||
CNHFAHCC_03771 | 3.8e-66 | yodA | S | tautomerase | ||
CNHFAHCC_03772 | 1.7e-57 | yodB | K | transcriptional | ||
CNHFAHCC_03773 | 4.8e-108 | yodC | C | nitroreductase | ||
CNHFAHCC_03774 | 3.8e-113 | mhqD | S | Carboxylesterase | ||
CNHFAHCC_03775 | 5.8e-174 | yodE | E | COG0346 Lactoylglutathione lyase and related lyases | ||
CNHFAHCC_03776 | 6.2e-28 | S | Protein of unknown function (DUF3311) | |||
CNHFAHCC_03777 | 4.2e-270 | yodF | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
CNHFAHCC_03778 | 1.9e-253 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
CNHFAHCC_03779 | 1.7e-128 | yodH | Q | Methyltransferase | ||
CNHFAHCC_03780 | 5.2e-24 | yodI | ||||
CNHFAHCC_03781 | 2.5e-139 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
CNHFAHCC_03782 | 3.2e-127 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
CNHFAHCC_03783 | 5.3e-09 | |||||
CNHFAHCC_03784 | 3.6e-54 | yodL | S | YodL-like | ||
CNHFAHCC_03785 | 5.4e-107 | yodM | 3.6.1.27 | I | Acid phosphatase homologues | |
CNHFAHCC_03786 | 2.8e-24 | yozD | S | YozD-like protein | ||
CNHFAHCC_03788 | 1.4e-124 | yodN | ||||
CNHFAHCC_03789 | 1.4e-36 | yozE | S | Belongs to the UPF0346 family | ||
CNHFAHCC_03790 | 2.9e-47 | yokU | S | YokU-like protein, putative antitoxin | ||
CNHFAHCC_03791 | 1.4e-278 | kamA | 5.4.3.2 | E | lysine 2,3-aminomutase | |
CNHFAHCC_03792 | 2.5e-155 | yodP | 2.3.1.264 | K | Acetyltransferase (GNAT) family | |
CNHFAHCC_03793 | 1.4e-258 | yodQ | 3.5.1.16 | E | Acetylornithine deacetylase | |
CNHFAHCC_03794 | 1.6e-117 | scoB | 2.8.3.5, 2.8.3.8, 2.8.3.9 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
CNHFAHCC_03795 | 8.1e-10 | yodS | 2.8.3.8, 2.8.3.9 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
CNHFAHCC_03796 | 1.6e-249 | yodT | H | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | ||
CNHFAHCC_03797 | 2.9e-145 | yiiD | K | acetyltransferase | ||
CNHFAHCC_03798 | 1e-256 | cgeD | M | maturation of the outermost layer of the spore | ||
CNHFAHCC_03799 | 3.5e-38 | cgeC | ||||
CNHFAHCC_03800 | 2.6e-65 | cgeA | ||||
CNHFAHCC_03801 | 3.3e-188 | cgeB | S | Spore maturation protein | ||
CNHFAHCC_03802 | 3.6e-213 | phy | 3.1.3.8 | I | Myo-inositol-hexaphosphate 3-phosphohydrolase | |
CNHFAHCC_03803 | 5.6e-125 | 4.2.1.115 | GM | Polysaccharide biosynthesis protein | ||
CNHFAHCC_03804 | 1.4e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
CNHFAHCC_03805 | 7e-103 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
CNHFAHCC_03806 | 1.6e-70 | ypoP | K | transcriptional | ||
CNHFAHCC_03807 | 2.6e-223 | mepA | V | MATE efflux family protein | ||
CNHFAHCC_03808 | 5.5e-29 | ypmT | S | Uncharacterized ympT | ||
CNHFAHCC_03809 | 5e-99 | ypmS | S | protein conserved in bacteria | ||
CNHFAHCC_03810 | 1.3e-137 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
CNHFAHCC_03811 | 3.2e-109 | ypmQ | S | protein SCO1 SenC PrrC, involved in biogenesis of respiratory and photosynthetic systems | ||
CNHFAHCC_03812 | 3.1e-40 | ypmP | S | Protein of unknown function (DUF2535) | ||
CNHFAHCC_03813 | 4.4e-244 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
CNHFAHCC_03814 | 1.6e-185 | pspF | K | Transcriptional regulator | ||
CNHFAHCC_03815 | 4.2e-110 | hlyIII | S | protein, Hemolysin III | ||
CNHFAHCC_03816 | 7.4e-112 | ypkP | 2.3.1.51 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
CNHFAHCC_03817 | 7.9e-96 | folA | 1.1.1.262, 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
CNHFAHCC_03818 | 4.3e-157 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
CNHFAHCC_03819 | 3.3e-92 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
CNHFAHCC_03820 | 7.8e-114 | ypjP | S | YpjP-like protein | ||
CNHFAHCC_03821 | 1.3e-145 | ypiP | 2.1.1.242 | AJ | Putative SAM-dependent methyltransferase | |
CNHFAHCC_03822 | 1.7e-75 | yphP | S | Belongs to the UPF0403 family | ||
CNHFAHCC_03823 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
CNHFAHCC_03824 | 1.8e-156 | ypgR | C | COG0694 Thioredoxin-like proteins and domains | ||
CNHFAHCC_03825 | 3.1e-110 | ypgQ | S | phosphohydrolase | ||
CNHFAHCC_03826 | 2.3e-89 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
CNHFAHCC_03827 | 7.3e-177 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
CNHFAHCC_03828 | 2e-216 | ugtP | 2.4.1.315 | GT28 | M | Processive glucosyltransferase involved in the biosynthesis of both the bilayer- and non-bilayer-forming membrane glucolipids. Is able to successively transfer up to three glucosyl residues to diacylglycerol (DAG), thereby catalyzing the formation of beta-monoglucosyl-DAG (3-O-(beta-D-glucopyranosyl)-1,2-diacyl- sn-glycerol), beta-diglucosyl-DAG (3-O-(beta-D-glucopyranosyl- beta-(1- 6)-D-glucopyranosyl)-1,2-diacyl-sn-glycerol) and beta- triglucosyl-DAG (3-O-(beta-D-glucopyranosyl-beta-(1- 6)-D- glucopyranosyl-beta-(1- 6)-D-glucopyranosyl)-1,2-diacyl-sn- glycerol). Beta-diglucosyl-DAG is the predominant glycolipid found in Bacillales and is also used as a membrane anchor for lipoteichoic acid (LTA) |
CNHFAHCC_03829 | 7.9e-31 | cspD | K | Cold-shock protein | ||
CNHFAHCC_03830 | 3.8e-16 | degR | ||||
CNHFAHCC_03831 | 6.6e-31 | S | Protein of unknown function (DUF2564) | |||
CNHFAHCC_03832 | 4.1e-29 | ypeQ | S | Zinc-finger | ||
CNHFAHCC_03833 | 1.2e-126 | ypeP | 3.1.26.4 | L | COG0328 Ribonuclease HI | |
CNHFAHCC_03834 | 5.4e-107 | ypdP | S | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
CNHFAHCC_03835 | 8.5e-69 | rnhA | 3.1.26.4 | L | Ribonuclease | |
CNHFAHCC_03837 | 1.5e-166 | polA | 2.7.7.7 | L | 5'3' exonuclease | |
CNHFAHCC_03838 | 2e-07 | |||||
CNHFAHCC_03839 | 1e-38 | ypbS | S | Protein of unknown function (DUF2533) | ||
CNHFAHCC_03840 | 0.0 | ypbR | S | Dynamin family | ||
CNHFAHCC_03841 | 5.1e-87 | ypbQ | S | protein conserved in bacteria | ||
CNHFAHCC_03842 | 4.4e-208 | bcsA | Q | Naringenin-chalcone synthase | ||
CNHFAHCC_03843 | 1.6e-228 | pbuX | F | xanthine | ||
CNHFAHCC_03844 | 8.8e-99 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
CNHFAHCC_03845 | 4.2e-294 | ypwA | 3.4.17.19 | E | Broad specificity carboxypetidase that releases amino acids sequentially from the C-terminus, including neutral, aromatic, polar and basic residues | |
CNHFAHCC_03846 | 5e-171 | kdgT | P | The 2-keto-3-deoxygluconate permease transports the degraded pectin products into the bacterial cell, where they serve as carbon and energy sources. This is a hydrogen coupled transport system | ||
CNHFAHCC_03847 | 7e-104 | eda | 2.7.1.45, 4.1.2.14, 4.1.3.42 | G | 2-dehydro-3-deoxy-phosphogluconate aldolase | |
CNHFAHCC_03848 | 2.9e-187 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
CNHFAHCC_03849 | 3.9e-187 | ptxS | K | transcriptional | ||
CNHFAHCC_03850 | 1.7e-159 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
CNHFAHCC_03851 | 7.1e-133 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_03852 | 0.0 | ypvA | 3.6.4.12 | KL | COG1199 Rad3-related DNA helicases | |
CNHFAHCC_03854 | 5.4e-225 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
CNHFAHCC_03855 | 2.8e-45 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
CNHFAHCC_03856 | 3.3e-97 | ypsA | S | Belongs to the UPF0398 family | ||
CNHFAHCC_03858 | 1.3e-237 | yprB | L | RNase_H superfamily | ||
CNHFAHCC_03859 | 0.0 | yprA | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
CNHFAHCC_03860 | 1.6e-81 | ypqE | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | |
CNHFAHCC_03861 | 8.6e-72 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
CNHFAHCC_03862 | 1.2e-48 | yppG | S | YppG-like protein | ||
CNHFAHCC_03864 | 2e-11 | yppE | S | Bacterial domain of unknown function (DUF1798) | ||
CNHFAHCC_03867 | 2.6e-188 | yppC | S | Protein of unknown function (DUF2515) | ||
CNHFAHCC_03868 | 1.2e-114 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
CNHFAHCC_03869 | 0.0 | ponA | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | M | penicillin-binding protein |
CNHFAHCC_03870 | 4.7e-93 | ypoC | ||||
CNHFAHCC_03871 | 2.2e-122 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
CNHFAHCC_03872 | 5.7e-129 | dnaD | L | DNA replication protein DnaD | ||
CNHFAHCC_03873 | 5.8e-252 | asnS | 6.1.1.22 | J | asparaginyl-tRNA | |
CNHFAHCC_03874 | 1.5e-222 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
CNHFAHCC_03875 | 3.4e-80 | ypmB | S | protein conserved in bacteria | ||
CNHFAHCC_03876 | 6.7e-23 | ypmA | S | Protein of unknown function (DUF4264) | ||
CNHFAHCC_03877 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
CNHFAHCC_03878 | 3.5e-64 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
CNHFAHCC_03879 | 1.2e-157 | panC | 2.7.4.25, 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
CNHFAHCC_03880 | 1.4e-150 | panB | 2.1.2.11 | H | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate | |
CNHFAHCC_03881 | 8.7e-184 | birA | 6.3.4.15 | K | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
CNHFAHCC_03882 | 4.4e-222 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
CNHFAHCC_03883 | 3.7e-210 | bshA | GT4 | M | N-acetyl-alpha-D-glucosaminyl L-malate synthase | |
CNHFAHCC_03884 | 6.9e-130 | bshB1 | S | proteins, LmbE homologs | ||
CNHFAHCC_03885 | 6.5e-72 | mgsA | 2.7.1.24, 4.2.3.3 | G | methylglyoxal synthase | |
CNHFAHCC_03886 | 6.3e-148 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
CNHFAHCC_03887 | 3.1e-56 | ypjD | 2.5.1.19 | S | Nucleotide pyrophosphohydrolase | |
CNHFAHCC_03888 | 8.1e-157 | ypjC | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
CNHFAHCC_03889 | 6.1e-143 | ypjB | S | sporulation protein | ||
CNHFAHCC_03890 | 2.1e-97 | ypjA | S | membrane | ||
CNHFAHCC_03891 | 1.5e-146 | qcrC | C | Menaquinol-cytochrome c reductase cytochrome b c subunit | ||
CNHFAHCC_03892 | 5.2e-127 | petB | C | COG1290 Cytochrome b subunit of the bc complex | ||
CNHFAHCC_03893 | 9.3e-97 | qcrA | C | Menaquinol-cytochrome c reductase | ||
CNHFAHCC_03894 | 8.5e-78 | ypiF | S | Protein of unknown function (DUF2487) | ||
CNHFAHCC_03895 | 2.8e-99 | ypiB | S | Belongs to the UPF0302 family | ||
CNHFAHCC_03896 | 4.1e-234 | S | COG0457 FOG TPR repeat | |||
CNHFAHCC_03897 | 4.7e-230 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
CNHFAHCC_03898 | 1.8e-201 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
CNHFAHCC_03899 | 2.1e-199 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
CNHFAHCC_03900 | 1.6e-135 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
CNHFAHCC_03901 | 3.9e-226 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
CNHFAHCC_03902 | 6.7e-119 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
CNHFAHCC_03903 | 4.7e-113 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
CNHFAHCC_03904 | 1.2e-180 | trpD | 2.4.2.18, 4.1.3.27 | E | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
CNHFAHCC_03905 | 6.6e-295 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
CNHFAHCC_03906 | 4.6e-64 | aroH | 2.7.4.25, 5.4.99.5 | E | Catalyzes the Claisen rearrangement of chorismate to prephenate. Probably involved in the aromatic amino acid biosynthesis | |
CNHFAHCC_03907 | 8.1e-207 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
CNHFAHCC_03908 | 5.5e-217 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
CNHFAHCC_03909 | 3.2e-143 | cheR | 2.1.1.80 | NT | COG1352 Methylase of chemotaxis methyl-accepting proteins | |
CNHFAHCC_03910 | 9.1e-80 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
CNHFAHCC_03911 | 4.5e-194 | hepT | 2.5.1.30, 2.5.1.83, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
CNHFAHCC_03912 | 8.6e-133 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
CNHFAHCC_03913 | 5.6e-138 | hepS | 2.5.1.30 | H | Heptaprenyl diphosphate synthase (HEPPP synthase) subunit 1 | |
CNHFAHCC_03914 | 2.3e-34 | mtrB | K | Required for transcription attenuation control in the Trp operon. This trans-acting factor seems to recognize a 10 bases nucleotide sequence in the Trp leader transcript causing transcription termination. Binds the leader RNA only in presence of L-tryptophan | ||
CNHFAHCC_03915 | 7.1e-101 | folE | 3.5.4.16 | H | GTP cyclohydrolase | |
CNHFAHCC_03916 | 4.7e-42 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
CNHFAHCC_03917 | 3.7e-279 | spoIVA | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | ||
CNHFAHCC_03918 | 5.4e-138 | yphF | ||||
CNHFAHCC_03919 | 1.6e-18 | yphE | S | Protein of unknown function (DUF2768) | ||
CNHFAHCC_03920 | 2.3e-190 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
CNHFAHCC_03921 | 3.9e-248 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
CNHFAHCC_03922 | 1.6e-28 | ypzH | ||||
CNHFAHCC_03923 | 2.5e-161 | seaA | S | YIEGIA protein | ||
CNHFAHCC_03924 | 1.3e-102 | yphA | ||||
CNHFAHCC_03925 | 1e-07 | S | YpzI-like protein | |||
CNHFAHCC_03926 | 4.1e-187 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
CNHFAHCC_03927 | 4.3e-206 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
CNHFAHCC_03928 | 1.9e-113 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
CNHFAHCC_03929 | 1.8e-23 | S | Family of unknown function (DUF5359) | |||
CNHFAHCC_03930 | 9.2e-113 | ypfA | M | Flagellar protein YcgR | ||
CNHFAHCC_03931 | 8.2e-105 | hemX | 2.1.1.107, 4.2.1.75 | H | sporulation protein | |
CNHFAHCC_03932 | 2.2e-134 | hemX | 2.1.1.107, 4.2.1.75 | H | sporulation protein | |
CNHFAHCC_03933 | 4.7e-155 | sleB | 3.5.1.28 | M | Spore cortex-lytic enzyme | |
CNHFAHCC_03934 | 1e-119 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
CNHFAHCC_03935 | 1.6e-174 | ypdA | 1.18.1.2, 1.19.1.1, 1.8.1.9 | O | COG0492 Thioredoxin reductase | |
CNHFAHCC_03936 | 7.3e-247 | gudB | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
CNHFAHCC_03937 | 1.3e-102 | mecB | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. Acts negatively in the development of competence by binding ComK and recruiting it to the ClpCP protease. When overexpressed, inhibits sporulation. Also involved in Spx degradation by ClpC | ||
CNHFAHCC_03938 | 1.8e-147 | ypbG | S | Calcineurin-like phosphoesterase superfamily domain | ||
CNHFAHCC_03939 | 2.8e-81 | ypbF | S | Protein of unknown function (DUF2663) | ||
CNHFAHCC_03940 | 4.6e-81 | ypbE | M | Lysin motif | ||
CNHFAHCC_03941 | 2.2e-100 | ypbD | S | metal-dependent membrane protease | ||
CNHFAHCC_03942 | 3.2e-286 | recQ | 3.6.4.12 | L | DNA helicase | |
CNHFAHCC_03943 | 3.8e-201 | ypbB | 5.1.3.1 | S | protein conserved in bacteria | |
CNHFAHCC_03944 | 4.7e-41 | fer | C | Ferredoxin | ||
CNHFAHCC_03945 | 5.8e-87 | fmnP | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
CNHFAHCC_03946 | 9.2e-10 | |||||
CNHFAHCC_03947 | 1.5e-294 | serA | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
CNHFAHCC_03948 | 9e-136 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
CNHFAHCC_03949 | 6.8e-201 | rsiX | ||||
CNHFAHCC_03950 | 2.6e-103 | sigX | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_03951 | 0.0 | resE | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_03952 | 2.3e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_03953 | 3.9e-215 | ccsA | O | 'COG0755 ABC-type transport system involved in cytochrome c biogenesis, permease component' | ||
CNHFAHCC_03954 | 0.0 | ccs1 | O | COG1333 ResB protein required for cytochrome c biosynthesis | ||
CNHFAHCC_03955 | 1.3e-99 | resA | CO | Thiol-disulfide oxidoreductase which is required in disulfide reduction during c-type cytochrome synthesis. May accept reducing equivalents from CcdA, leading to breakage of disulfide bonds in apocytochrome c | ||
CNHFAHCC_03956 | 6.9e-133 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
CNHFAHCC_03957 | 1.9e-87 | spmB | S | Spore maturation protein | ||
CNHFAHCC_03958 | 3.5e-103 | spmA | S | Spore maturation protein | ||
CNHFAHCC_03959 | 1.2e-213 | dacB | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
CNHFAHCC_03960 | 4e-98 | ypuI | S | Protein of unknown function (DUF3907) | ||
CNHFAHCC_03961 | 1.9e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
CNHFAHCC_03962 | 4.5e-130 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
CNHFAHCC_03963 | 4.5e-94 | ypuF | S | Domain of unknown function (DUF309) | ||
CNHFAHCC_03964 | 4.5e-64 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
CNHFAHCC_03965 | 3.9e-81 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
CNHFAHCC_03966 | 9.8e-230 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
CNHFAHCC_03967 | 1.5e-115 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
CNHFAHCC_03968 | 1.3e-204 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
CNHFAHCC_03969 | 6e-55 | ypuD | ||||
CNHFAHCC_03970 | 5.2e-101 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
CNHFAHCC_03971 | 2.3e-33 | yhcC | S | nucleic-acid-binding protein containing a Zn-ribbon domain | ||
CNHFAHCC_03972 | 1.5e-17 | S | SNARE associated Golgi protein | |||
CNHFAHCC_03976 | 8e-81 | ppiB | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
CNHFAHCC_03977 | 4.6e-150 | ypuA | S | Secreted protein | ||
CNHFAHCC_03978 | 5.2e-256 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
CNHFAHCC_03979 | 1.4e-273 | spoVAF | EG | Stage V sporulation protein AF | ||
CNHFAHCC_03980 | 1.4e-110 | spoVAEA | S | stage V sporulation protein | ||
CNHFAHCC_03981 | 2.2e-57 | spoVAEB | S | stage V sporulation protein | ||
CNHFAHCC_03982 | 9e-192 | spoVAD | I | Stage V sporulation protein AD | ||
CNHFAHCC_03983 | 2.3e-78 | spoVAC | S | stage V sporulation protein AC | ||
CNHFAHCC_03984 | 1e-67 | spoVAB | S | Stage V sporulation protein AB | ||
CNHFAHCC_03985 | 7.4e-112 | spoVAA | S | Stage V sporulation protein AA | ||
CNHFAHCC_03986 | 2.4e-136 | sigF | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_03987 | 1.8e-75 | spoIIAB | 2.7.11.1 | F | Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition | |
CNHFAHCC_03988 | 3.9e-57 | spoIIAA | T | Belongs to the anti-sigma-factor antagonist family | ||
CNHFAHCC_03989 | 2.8e-213 | dacF | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
CNHFAHCC_03990 | 1.7e-148 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
CNHFAHCC_03991 | 1.2e-232 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
CNHFAHCC_03992 | 2.6e-166 | xerD | L | recombinase XerD | ||
CNHFAHCC_03993 | 3.7e-37 | S | Protein of unknown function (DUF4227) | |||
CNHFAHCC_03994 | 2.4e-80 | fur | P | Belongs to the Fur family | ||
CNHFAHCC_03995 | 2.3e-108 | spoIIM | S | Required for complete septum migration and engulfment of the forespore compartment during sporulation. Required for stabilizing and recruiting of SpoIIP to the septal membrane | ||
CNHFAHCC_03996 | 2e-32 | yqkK | ||||
CNHFAHCC_03997 | 5.5e-242 | mleA | 1.1.1.38 | C | malic enzyme | |
CNHFAHCC_03998 | 3.1e-235 | mleN | C | Na H antiporter | ||
CNHFAHCC_03999 | 2.9e-268 | aspA | 4.2.1.2, 4.3.1.1 | E | Aspartate ammonia-lyase | |
CNHFAHCC_04000 | 3.6e-185 | ansA | 3.5.1.1 | EJ | L-asparaginase | |
CNHFAHCC_04001 | 4.5e-58 | ansR | K | Transcriptional regulator | ||
CNHFAHCC_04002 | 3e-223 | yqxK | 3.6.4.12 | L | DNA helicase | |
CNHFAHCC_04003 | 1.2e-92 | nudF | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
CNHFAHCC_04005 | 4.4e-169 | yqkF | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | ||
CNHFAHCC_04006 | 4e-14 | yqkE | S | Protein of unknown function (DUF3886) | ||
CNHFAHCC_04007 | 2.4e-175 | yqkD | S | COG1073 Hydrolases of the alpha beta superfamily | ||
CNHFAHCC_04008 | 9.4e-39 | yqkC | S | Protein of unknown function (DUF2552) | ||
CNHFAHCC_04009 | 2.8e-54 | yqkB | S | Belongs to the HesB IscA family | ||
CNHFAHCC_04010 | 4.7e-196 | yqkA | K | GrpB protein | ||
CNHFAHCC_04011 | 8e-60 | yqjZ | 2.3.1.128, 2.5.1.18 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
CNHFAHCC_04012 | 3.6e-87 | yqjY | K | acetyltransferase | ||
CNHFAHCC_04013 | 2.2e-49 | S | YolD-like protein | |||
CNHFAHCC_04014 | 3.1e-239 | polYB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
CNHFAHCC_04016 | 5.2e-226 | yqjV | G | Major Facilitator Superfamily | ||
CNHFAHCC_04018 | 7.2e-73 | yqjT | 3.1.26.4 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
CNHFAHCC_04019 | 2.4e-178 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
CNHFAHCC_04020 | 2.4e-264 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
CNHFAHCC_04021 | 3.5e-143 | yqjQ | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
CNHFAHCC_04022 | 3.4e-180 | yqjP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
CNHFAHCC_04023 | 8.6e-148 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
CNHFAHCC_04024 | 0.0 | rocB | E | arginine degradation protein | ||
CNHFAHCC_04025 | 1.4e-192 | namA | 1.6.99.1 | C | Catalyzes the reduction of the double bond of an array of alpha,beta-unsaturated aldehydes and ketones. It also reduces the nitro group of nitroester and nitroaromatic compounds. It could have a role in detoxification processes | |
CNHFAHCC_04026 | 9.6e-146 | yqjL | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | ||
CNHFAHCC_04027 | 2.9e-173 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
CNHFAHCC_04028 | 1.6e-290 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
CNHFAHCC_04029 | 6.9e-267 | gnd | 1.1.1.343, 1.1.1.44 | G | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
CNHFAHCC_04030 | 7.3e-236 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
CNHFAHCC_04031 | 4.5e-24 | yqzJ | ||||
CNHFAHCC_04032 | 5.7e-144 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
CNHFAHCC_04033 | 3.6e-142 | yqjF | S | Uncharacterized conserved protein (COG2071) | ||
CNHFAHCC_04034 | 1.6e-202 | yqjE | 3.4.11.4 | E | COG2195 Di- and tripeptidases | |
CNHFAHCC_04035 | 4.4e-291 | mmdA | 2.1.3.15, 6.4.1.3 | I | COG4799 Acetyl-CoA carboxylase, carboxyltransferase component (subunits alpha and beta) | |
CNHFAHCC_04036 | 2.2e-75 | mce | 4.4.1.5, 5.1.99.1, 5.4.99.2 | E | COG0346 Lactoylglutathione lyase and related lyases | |
CNHFAHCC_04038 | 1.4e-98 | yqjB | S | protein conserved in bacteria | ||
CNHFAHCC_04039 | 1.1e-175 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
CNHFAHCC_04040 | 2e-129 | artM | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
CNHFAHCC_04041 | 6.2e-109 | artQ | E | COG0765 ABC-type amino acid transport system, permease component | ||
CNHFAHCC_04042 | 6.3e-137 | artP | ET | Belongs to the bacterial solute-binding protein 3 family | ||
CNHFAHCC_04043 | 5.9e-76 | yqiW | S | Belongs to the UPF0403 family | ||
CNHFAHCC_04044 | 8.8e-167 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
CNHFAHCC_04045 | 7.9e-208 | norA | EGP | Major facilitator Superfamily | ||
CNHFAHCC_04046 | 2.6e-152 | bmrR | K | helix_turn_helix, mercury resistance | ||
CNHFAHCC_04047 | 3.5e-233 | bfmBB | 2.3.1.168, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
CNHFAHCC_04048 | 3.2e-184 | bfmBAB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
CNHFAHCC_04049 | 1.9e-186 | bfmBAA | 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
CNHFAHCC_04050 | 3.4e-269 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
CNHFAHCC_04051 | 1.2e-202 | buk | 2.7.2.7 | C | Belongs to the acetokinase family | |
CNHFAHCC_04052 | 2.2e-207 | ldh | 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
CNHFAHCC_04053 | 7.1e-156 | pta | 2.3.1.19, 2.3.1.8 | C | phosphate butyryltransferase | |
CNHFAHCC_04054 | 0.0 | bkdR | 2.7.13.3 | KT | Transcriptional regulator | |
CNHFAHCC_04055 | 4e-34 | yqzF | S | Protein of unknown function (DUF2627) | ||
CNHFAHCC_04056 | 7.1e-164 | prpB | 4.1.3.30 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
CNHFAHCC_04057 | 5.7e-277 | prpD | 4.2.1.79 | S | 2-methylcitrate dehydratase | |
CNHFAHCC_04058 | 8.1e-210 | prpC | 2.3.3.1, 2.3.3.5 | C | Belongs to the citrate synthase family | |
CNHFAHCC_04059 | 1.8e-212 | mmgC | I | acyl-CoA dehydrogenase | ||
CNHFAHCC_04060 | 4.7e-157 | hbdA | 1.1.1.157 | I | Dehydrogenase | |
CNHFAHCC_04061 | 1.2e-219 | mmgA | 2.3.1.9 | I | Belongs to the thiolase family | |
CNHFAHCC_04062 | 1.8e-133 | yqiK | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
CNHFAHCC_04063 | 5.4e-107 | amiC | 3.5.1.28 | M | Cell wall hydrolase autolysin | |
CNHFAHCC_04064 | 5.9e-27 | |||||
CNHFAHCC_04065 | 1.3e-215 | yqiG | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | ||
CNHFAHCC_04066 | 3.2e-144 | KT | May play the central regulatory role in sporulation. It may be an element of the effector pathway responsible for the activation of sporulation genes in response to nutritional stress. Spo0A may act in concert with spo0H (a sigma factor) to control the expression of some genes that are critical to the sporulation process | |||
CNHFAHCC_04067 | 1.2e-238 | rseP | 3.4.21.116 | M | Stage IV sporulation protein B | |
CNHFAHCC_04068 | 0.0 | recN | L | May be involved in recombinational repair of damaged DNA | ||
CNHFAHCC_04069 | 1.7e-78 | argR | K | Regulates arginine biosynthesis genes | ||
CNHFAHCC_04070 | 6.6e-156 | rrmJ | 2.1.1.226, 2.1.1.227 | J | rRNA methylase | |
CNHFAHCC_04071 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
CNHFAHCC_04072 | 7.7e-163 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
CNHFAHCC_04073 | 5.8e-39 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
CNHFAHCC_04074 | 2.9e-246 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
CNHFAHCC_04075 | 1e-156 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
CNHFAHCC_04076 | 1.9e-65 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
CNHFAHCC_04077 | 2.1e-67 | yqhY | S | protein conserved in bacteria | ||
CNHFAHCC_04078 | 1.5e-255 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
CNHFAHCC_04079 | 1.5e-64 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
CNHFAHCC_04080 | 9.9e-91 | spoIIIAH | S | SpoIIIAH-like protein | ||
CNHFAHCC_04081 | 6.9e-103 | spoIIIAG | S | stage III sporulation protein AG | ||
CNHFAHCC_04082 | 3.1e-102 | spoIIIAF | S | Stage III sporulation protein AF (Spore_III_AF) | ||
CNHFAHCC_04083 | 1.3e-197 | spoIIIAE | S | stage III sporulation protein AE | ||
CNHFAHCC_04084 | 2.3e-58 | spoIIIAD | S | Stage III sporulation protein AD | ||
CNHFAHCC_04085 | 7.6e-29 | spoIIIAC | S | stage III sporulation protein AC | ||
CNHFAHCC_04086 | 2.9e-85 | spoIIIAB | S | Stage III sporulation protein | ||
CNHFAHCC_04087 | 4.7e-171 | spoIIIAA | S | stage III sporulation protein AA | ||
CNHFAHCC_04088 | 7.9e-37 | yqhV | S | Protein of unknown function (DUF2619) | ||
CNHFAHCC_04089 | 5.4e-98 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
CNHFAHCC_04090 | 8.9e-174 | yqhT | 3.4.11.9, 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
CNHFAHCC_04091 | 1.5e-77 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
CNHFAHCC_04092 | 2.3e-93 | yqhR | S | Conserved membrane protein YqhR | ||
CNHFAHCC_04093 | 1.5e-172 | yqhQ | S | Protein of unknown function (DUF1385) | ||
CNHFAHCC_04094 | 2.2e-61 | yqhP | ||||
CNHFAHCC_04095 | 8.1e-165 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
CNHFAHCC_04096 | 9.4e-74 | mntR | K | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon | ||
CNHFAHCC_04097 | 5.2e-161 | lipM | 6.3.1.20 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation | |
CNHFAHCC_04098 | 2.3e-63 | yqhL | P | COG0607 Rhodanese-related sulfurtransferase | ||
CNHFAHCC_04099 | 2.8e-287 | gcvPB | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
CNHFAHCC_04100 | 3.4e-255 | gcvPA | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
CNHFAHCC_04101 | 1.1e-206 | gcvT | 1.4.4.2, 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
CNHFAHCC_04102 | 0.0 | yqhH | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
CNHFAHCC_04103 | 2.5e-152 | yqhG | S | Bacterial protein YqhG of unknown function | ||
CNHFAHCC_04104 | 1.2e-24 | sinI | S | Anti-repressor SinI | ||
CNHFAHCC_04105 | 1e-54 | sinR | K | transcriptional | ||
CNHFAHCC_04106 | 2.3e-142 | tasA | S | Cell division protein FtsN | ||
CNHFAHCC_04107 | 6.7e-59 | sipW | 3.4.21.89 | U | Signal peptidase | |
CNHFAHCC_04108 | 2e-70 | yqxM | ||||
CNHFAHCC_04109 | 2.7e-35 | yqxM | ||||
CNHFAHCC_04110 | 7.3e-54 | yqzG | S | Protein of unknown function (DUF3889) | ||
CNHFAHCC_04111 | 1.4e-26 | yqzE | S | YqzE-like protein | ||
CNHFAHCC_04112 | 3.7e-42 | S | ComG operon protein 7 | |||
CNHFAHCC_04113 | 5.5e-49 | comGF | U | Putative Competence protein ComGF | ||
CNHFAHCC_04114 | 1.1e-59 | comGE | ||||
CNHFAHCC_04115 | 4.8e-71 | gspH | NU | protein transport across the cell outer membrane | ||
CNHFAHCC_04116 | 1.4e-47 | comGC | U | Required for transformation and DNA binding | ||
CNHFAHCC_04117 | 1.6e-175 | comGB | NU | COG1459 Type II secretory pathway, component PulF | ||
CNHFAHCC_04118 | 3.9e-201 | comGA | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
CNHFAHCC_04119 | 7.2e-175 | corA | P | Mg2 transporter protein | ||
CNHFAHCC_04120 | 4.3e-242 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
CNHFAHCC_04121 | 1.7e-151 | yqhA | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | ||
CNHFAHCC_04123 | 7.8e-64 | yqgZ | 1.20.4.1 | P | Belongs to the ArsC family | |
CNHFAHCC_04124 | 1.8e-37 | yqgY | S | Protein of unknown function (DUF2626) | ||
CNHFAHCC_04125 | 4.3e-120 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
CNHFAHCC_04126 | 8.9e-23 | yqgW | S | Protein of unknown function (DUF2759) | ||
CNHFAHCC_04127 | 6.9e-50 | yqgV | S | Thiamine-binding protein | ||
CNHFAHCC_04128 | 2.7e-199 | yqgU | ||||
CNHFAHCC_04129 | 1.4e-222 | yqgT | 3.4.19.11 | E | Gamma-D-glutamyl-L-diamino acid endopeptidase | |
CNHFAHCC_04130 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
CNHFAHCC_04131 | 5.2e-181 | glcK | 2.7.1.2 | G | Glucokinase | |
CNHFAHCC_04132 | 4.3e-33 | yqgQ | S | Protein conserved in bacteria | ||
CNHFAHCC_04133 | 1.4e-268 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
CNHFAHCC_04134 | 2.5e-09 | yqgO | ||||
CNHFAHCC_04135 | 2.7e-105 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
CNHFAHCC_04136 | 9.4e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
CNHFAHCC_04137 | 2.9e-201 | yqgM | 2.4.1.11, 2.4.1.18 | GH57,GT4 | M | Glycosyl transferases group 1 |
CNHFAHCC_04139 | 9.2e-51 | yqzD | ||||
CNHFAHCC_04140 | 1.9e-75 | yqzC | S | YceG-like family | ||
CNHFAHCC_04141 | 9.8e-146 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
CNHFAHCC_04142 | 9e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
CNHFAHCC_04143 | 4.4e-158 | pstA | P | Phosphate transport system permease | ||
CNHFAHCC_04144 | 1.3e-160 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
CNHFAHCC_04145 | 9.8e-144 | pstS | P | Phosphate | ||
CNHFAHCC_04146 | 0.0 | pbpA | 3.4.16.4 | M | penicillin-binding protein | |
CNHFAHCC_04147 | 2.5e-231 | yqgE | EGP | Major facilitator superfamily | ||
CNHFAHCC_04148 | 6.3e-116 | sodA | 1.15.1.1 | P | radicals which are normally produced within the cells and which are toxic to biological systems | |
CNHFAHCC_04149 | 4e-73 | yqgC | S | protein conserved in bacteria | ||
CNHFAHCC_04150 | 8.5e-134 | yqgB | S | Protein of unknown function (DUF1189) | ||
CNHFAHCC_04151 | 2.2e-75 | yqgA | ||||
CNHFAHCC_04152 | 5.2e-47 | yqfZ | M | LysM domain | ||
CNHFAHCC_04153 | 2.8e-202 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
CNHFAHCC_04154 | 5.8e-63 | yqfX | S | membrane | ||
CNHFAHCC_04155 | 1.2e-108 | yqfW | S | Belongs to the 5'(3')-deoxyribonucleotidase family | ||
CNHFAHCC_04156 | 1.9e-77 | zur | P | Belongs to the Fur family | ||
CNHFAHCC_04157 | 1.6e-157 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
CNHFAHCC_04158 | 2.1e-36 | yqfT | S | Protein of unknown function (DUF2624) | ||
CNHFAHCC_04159 | 8.8e-167 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
CNHFAHCC_04160 | 1.7e-243 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
CNHFAHCC_04161 | 2.9e-14 | yqfQ | S | YqfQ-like protein | ||
CNHFAHCC_04162 | 2.6e-177 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
CNHFAHCC_04163 | 5.1e-212 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
CNHFAHCC_04164 | 3.5e-112 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
CNHFAHCC_04165 | 2.2e-60 | cccA | C | COG2010 Cytochrome c, mono- and diheme variants | ||
CNHFAHCC_04166 | 1.2e-200 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
CNHFAHCC_04167 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
CNHFAHCC_04168 | 4.5e-88 | yaiI | S | Belongs to the UPF0178 family | ||
CNHFAHCC_04169 | 5.8e-149 | yqfL | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
CNHFAHCC_04170 | 4.5e-112 | ccpN | K | CBS domain | ||
CNHFAHCC_04171 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
CNHFAHCC_04172 | 3.3e-174 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
CNHFAHCC_04173 | 4.8e-145 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
CNHFAHCC_04174 | 8.4e-19 | S | YqzL-like protein | |||
CNHFAHCC_04175 | 3.1e-167 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
CNHFAHCC_04176 | 7.1e-71 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
CNHFAHCC_04177 | 1.6e-61 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
CNHFAHCC_04178 | 5.1e-81 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
CNHFAHCC_04179 | 0.0 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
CNHFAHCC_04181 | 1.1e-175 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
CNHFAHCC_04182 | 1.5e-185 | yqfD | 3.1.3.102, 3.1.3.104 | S | Stage IV sporulation | |
CNHFAHCC_04183 | 2.7e-45 | yqfC | S | sporulation protein YqfC | ||
CNHFAHCC_04184 | 6e-25 | yqfB | ||||
CNHFAHCC_04185 | 4.3e-122 | yqfA | S | UPF0365 protein | ||
CNHFAHCC_04186 | 5.4e-229 | yqeZ | O | COG1030 Membrane-bound serine protease (ClpP class) | ||
CNHFAHCC_04187 | 2.5e-61 | yqeY | S | Yqey-like protein | ||
CNHFAHCC_04188 | 1.2e-19 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
CNHFAHCC_04189 | 1.6e-158 | yqeW | P | COG1283 Na phosphate symporter | ||
CNHFAHCC_04190 | 2.1e-260 | yqeV | 2.8.4.5 | J | ribosomal protein S12 methylthiotransferase | |
CNHFAHCC_04191 | 1.4e-141 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
CNHFAHCC_04192 | 5.4e-175 | prmA | J | Methylates ribosomal protein L11 | ||
CNHFAHCC_04193 | 4.2e-182 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
CNHFAHCC_04194 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
CNHFAHCC_04195 | 3.8e-75 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
CNHFAHCC_04196 | 4.7e-188 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
CNHFAHCC_04197 | 4.8e-218 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
CNHFAHCC_04198 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
CNHFAHCC_04199 | 1e-54 | yqxA | S | Protein of unknown function (DUF3679) | ||
CNHFAHCC_04200 | 6.9e-223 | spoIIP | M | stage II sporulation protein P | ||
CNHFAHCC_04201 | 1.3e-204 | gpr | 3.4.24.78 | C | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | |
CNHFAHCC_04202 | 9.7e-37 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
CNHFAHCC_04203 | 1.1e-189 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
CNHFAHCC_04204 | 0.0 | comEC | S | Competence protein ComEC | ||
CNHFAHCC_04205 | 2.1e-105 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
CNHFAHCC_04206 | 3e-105 | wza | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
CNHFAHCC_04207 | 8.4e-148 | comER | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | ||
CNHFAHCC_04208 | 2.9e-139 | yqeM | Q | Methyltransferase | ||
CNHFAHCC_04209 | 6.9e-62 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
CNHFAHCC_04210 | 7.4e-103 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
CNHFAHCC_04211 | 2.7e-108 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
CNHFAHCC_04212 | 2.1e-45 | yhbY | J | RNA-binding protein containing KH domain, possibly ribosomal protein | ||
CNHFAHCC_04213 | 2.7e-157 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
CNHFAHCC_04214 | 9.1e-214 | yqeH | S | In Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
CNHFAHCC_04215 | 5.3e-95 | yqeG | S | hydrolase of the HAD superfamily | ||
CNHFAHCC_04217 | 6.2e-142 | yqeF | E | GDSL-like Lipase/Acylhydrolase | ||
CNHFAHCC_04218 | 2.1e-137 | xlyA | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
CNHFAHCC_04219 | 4.7e-106 | yqeD | S | SNARE associated Golgi protein | ||
CNHFAHCC_04220 | 1.2e-171 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase | |
CNHFAHCC_04221 | 2.3e-133 | yqeB | ||||
CNHFAHCC_04222 | 1.1e-74 | nucB | M | Deoxyribonuclease NucA/NucB | ||
CNHFAHCC_04223 | 3.1e-125 | sigK | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_04224 | 2e-68 | psiE | S | Protein PsiE homolog | ||
CNHFAHCC_04225 | 9e-237 | yrkQ | T | Histidine kinase | ||
CNHFAHCC_04226 | 1.1e-127 | T | Transcriptional regulator | |||
CNHFAHCC_04227 | 8.2e-224 | yrkO | P | Protein of unknown function (DUF418) | ||
CNHFAHCC_04228 | 6e-105 | yrkN | K | Acetyltransferase (GNAT) family | ||
CNHFAHCC_04229 | 1.5e-97 | ywrO | S | Flavodoxin-like fold | ||
CNHFAHCC_04230 | 2.8e-79 | S | Protein of unknown function with HXXEE motif | |||
CNHFAHCC_04231 | 4.3e-117 | yrkJ | S | membrane transporter protein | ||
CNHFAHCC_04232 | 2.4e-36 | yrkI | O | Belongs to the sulfur carrier protein TusA family | ||
CNHFAHCC_04233 | 1.1e-219 | yrkH | P | Rhodanese Homology Domain | ||
CNHFAHCC_04234 | 3e-08 | perX | S | DsrE/DsrF-like family | ||
CNHFAHCC_04235 | 1.7e-99 | yrkF | OP | Belongs to the sulfur carrier protein TusA family | ||
CNHFAHCC_04236 | 5.1e-84 | yrkE | O | DsrE/DsrF/DrsH-like family | ||
CNHFAHCC_04237 | 7.8e-39 | yrkD | S | protein conserved in bacteria | ||
CNHFAHCC_04238 | 2e-28 | |||||
CNHFAHCC_04239 | 2.6e-108 | yrkC | G | Cupin domain | ||
CNHFAHCC_04240 | 4.8e-151 | bltR | K | helix_turn_helix, mercury resistance | ||
CNHFAHCC_04241 | 3.5e-211 | blt | EGP | Major facilitator Superfamily | ||
CNHFAHCC_04242 | 1.4e-83 | bltD | 2.3.1.57 | K | FR47-like protein | |
CNHFAHCC_04243 | 4.5e-236 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
CNHFAHCC_04244 | 2.1e-17 | S | YrzO-like protein | |||
CNHFAHCC_04245 | 1.7e-171 | yrdR | EG | EamA-like transporter family | ||
CNHFAHCC_04246 | 5.9e-160 | yrdQ | K | Transcriptional regulator | ||
CNHFAHCC_04247 | 2e-199 | trkA | P | Oxidoreductase | ||
CNHFAHCC_04248 | 3.5e-158 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
CNHFAHCC_04249 | 1.3e-66 | yodA | S | tautomerase | ||
CNHFAHCC_04250 | 7.7e-163 | gltR | K | LysR substrate binding domain | ||
CNHFAHCC_04252 | 1.5e-231 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
CNHFAHCC_04253 | 2.5e-50 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
CNHFAHCC_04254 | 3.3e-138 | azlC | E | AzlC protein | ||
CNHFAHCC_04255 | 2.2e-79 | bkdR | K | helix_turn_helix ASNC type | ||
CNHFAHCC_04256 | 4.1e-46 | yrdF | K | ribonuclease inhibitor | ||
CNHFAHCC_04257 | 4.1e-231 | cypA | C | Cytochrome P450 | ||
CNHFAHCC_04260 | 3.1e-101 | yrdC | 3.5.1.19 | Q | Isochorismatase family | |
CNHFAHCC_04261 | 1.9e-57 | S | Protein of unknown function (DUF2568) | |||
CNHFAHCC_04262 | 1.2e-91 | yrdA | S | DinB family | ||
CNHFAHCC_04263 | 7.6e-168 | aadK | G | Streptomycin adenylyltransferase | ||
CNHFAHCC_04264 | 1.5e-194 | yrpB | 1.13.12.16 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | |
CNHFAHCC_04265 | 4.2e-141 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
CNHFAHCC_04266 | 3e-125 | yrpD | S | Domain of unknown function, YrpD | ||
CNHFAHCC_04268 | 5.4e-117 | adcA | S | ZinT (YodA) periplasmic lipocalin-like zinc-recruitment | ||
CNHFAHCC_04269 | 6.3e-96 | sigZ | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_04270 | 4.5e-188 | yrpG | C | Aldo/keto reductase family | ||
CNHFAHCC_04271 | 2e-08 | yrpG | C | Aldo/keto reductase family | ||
CNHFAHCC_04272 | 9.5e-226 | yraO | C | Citrate transporter | ||
CNHFAHCC_04273 | 1.2e-163 | yraN | K | Transcriptional regulator | ||
CNHFAHCC_04274 | 2.4e-206 | yraM | S | PrpF protein | ||
CNHFAHCC_04276 | 2.7e-157 | csn | 3.2.1.132 | M | Aids in the defense against invading fungal pathogens by degrading their cell wall chitosan | |
CNHFAHCC_04277 | 7.6e-42 | yraL | S | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_04278 | 3.2e-155 | S | Alpha beta hydrolase | |||
CNHFAHCC_04279 | 2.6e-61 | T | sh3 domain protein | |||
CNHFAHCC_04280 | 2.4e-61 | T | sh3 domain protein | |||
CNHFAHCC_04281 | 1.3e-66 | E | Glyoxalase-like domain | |||
CNHFAHCC_04282 | 5.3e-37 | yraG | ||||
CNHFAHCC_04283 | 6.4e-63 | yraF | M | Spore coat protein | ||
CNHFAHCC_04284 | 2.9e-223 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284, 1.2.1.46 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
CNHFAHCC_04285 | 2.6e-26 | yraE | ||||
CNHFAHCC_04286 | 1.1e-49 | yraD | M | Spore coat protein | ||
CNHFAHCC_04287 | 4.3e-47 | yraB | K | helix_turn_helix, mercury resistance | ||
CNHFAHCC_04288 | 3.2e-29 | yphJ | 4.1.1.44 | S | peroxiredoxin activity | |
CNHFAHCC_04289 | 1.9e-200 | adhA | 1.1.1.1 | C | alcohol dehydrogenase | |
CNHFAHCC_04290 | 5e-90 | yhbO | 1.11.1.6, 3.5.1.124 | S | protease | |
CNHFAHCC_04291 | 0.0 | sacC | 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
CNHFAHCC_04292 | 1.5e-152 | manZ | G | COG3716 Phosphotransferase system, mannose fructose N-acetylgalactosamine-specific component IID | ||
CNHFAHCC_04293 | 4.9e-116 | manY | G | COG3715 Phosphotransferase system, mannose fructose N-acetylgalactosamine-specific component IIC | ||
CNHFAHCC_04294 | 8.2e-82 | levE | 2.7.1.202 | G | PTS system mannose fructose sorbose family | |
CNHFAHCC_04295 | 3.9e-75 | levD | 2.7.1.202 | G | PTS system fructose IIA component | |
CNHFAHCC_04296 | 0.0 | levR | K | PTS system fructose IIA component | ||
CNHFAHCC_04297 | 1.6e-255 | cycA | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_04298 | 3.6e-106 | yrhP | E | LysE type translocator | ||
CNHFAHCC_04299 | 1.1e-150 | yrhO | K | Archaeal transcriptional regulator TrmB | ||
CNHFAHCC_04300 | 4.3e-86 | sigV | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_04301 | 1.7e-151 | rsiV | S | Protein of unknown function (DUF3298) | ||
CNHFAHCC_04302 | 0.0 | yrhL | I | Acyltransferase family | ||
CNHFAHCC_04303 | 1.5e-46 | yrhK | S | YrhK-like protein | ||
CNHFAHCC_04304 | 0.0 | cypD | 1.14.14.1, 1.6.2.4 | C | Belongs to the cytochrome P450 family | |
CNHFAHCC_04305 | 4.8e-105 | Z012_03230 | K | Tetracycline repressor, C-terminal all-alpha domain | ||
CNHFAHCC_04306 | 4.5e-97 | yrhH | Q | methyltransferase | ||
CNHFAHCC_04309 | 1.8e-142 | focA | P | Formate nitrite | ||
CNHFAHCC_04310 | 7.8e-61 | yrhF | S | Uncharacterized conserved protein (DUF2294) | ||
CNHFAHCC_04311 | 0.0 | fdhA | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase (NAD+) activity | |
CNHFAHCC_04312 | 1.4e-78 | yrhD | S | Protein of unknown function (DUF1641) | ||
CNHFAHCC_04313 | 1.5e-32 | yrhC | S | YrhC-like protein | ||
CNHFAHCC_04314 | 2.6e-211 | mccB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
CNHFAHCC_04315 | 1.2e-171 | mccA | 2.5.1.134, 2.5.1.47 | E | Cysteine synthase | |
CNHFAHCC_04316 | 4.2e-124 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
CNHFAHCC_04317 | 1.2e-120 | yrrT | 4.4.1.21 | Q | Could be a S-adenosyl-L-methionine-dependent methyltransferase | |
CNHFAHCC_04318 | 7e-27 | yrzA | S | Protein of unknown function (DUF2536) | ||
CNHFAHCC_04319 | 4.2e-63 | yrrS | S | Protein of unknown function (DUF1510) | ||
CNHFAHCC_04320 | 0.0 | pbpI | 3.4.16.4 | M | Penicillin-binding Protein | |
CNHFAHCC_04321 | 2.4e-78 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
CNHFAHCC_04322 | 4.7e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
CNHFAHCC_04323 | 2.7e-246 | yegQ | O | COG0826 Collagenase and related proteases | ||
CNHFAHCC_04324 | 7.8e-174 | yegQ | O | Peptidase U32 | ||
CNHFAHCC_04325 | 5.9e-120 | yrrM | 2.1.1.104 | S | O-methyltransferase | |
CNHFAHCC_04326 | 1.6e-183 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
CNHFAHCC_04327 | 1.2e-45 | yrzB | S | Belongs to the UPF0473 family | ||
CNHFAHCC_04328 | 2.1e-70 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
CNHFAHCC_04329 | 1.7e-41 | yrzL | S | Belongs to the UPF0297 family | ||
CNHFAHCC_04330 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
CNHFAHCC_04331 | 2.7e-170 | yrrI | S | AI-2E family transporter | ||
CNHFAHCC_04332 | 1.3e-131 | glnQ | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
CNHFAHCC_04333 | 5.1e-145 | glnH | ET | Belongs to the bacterial solute-binding protein 3 family | ||
CNHFAHCC_04334 | 3.6e-109 | gluC | P | ABC transporter | ||
CNHFAHCC_04335 | 7.6e-107 | glnP | P | ABC transporter | ||
CNHFAHCC_04336 | 8e-08 | S | Protein of unknown function (DUF3918) | |||
CNHFAHCC_04337 | 9.8e-31 | yrzR | ||||
CNHFAHCC_04338 | 1.2e-94 | yrrD | S | protein conserved in bacteria | ||
CNHFAHCC_04339 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
CNHFAHCC_04340 | 1.4e-15 | S | COG0457 FOG TPR repeat | |||
CNHFAHCC_04341 | 2.3e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
CNHFAHCC_04342 | 4.7e-213 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
CNHFAHCC_04343 | 1.2e-70 | cymR | K | Transcriptional regulator | ||
CNHFAHCC_04344 | 2e-236 | rarA | L | COG2256 ATPase related to the helicase subunit of the Holliday junction resolvase | ||
CNHFAHCC_04345 | 2.8e-137 | yrvM | H | COG1179 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | ||
CNHFAHCC_04346 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
CNHFAHCC_04347 | 5.2e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
CNHFAHCC_04349 | 3.9e-263 | lytH | 3.5.1.28 | M | COG3103 SH3 domain protein | |
CNHFAHCC_04350 | 1.9e-68 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
CNHFAHCC_04351 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
CNHFAHCC_04352 | 5.9e-91 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
CNHFAHCC_04353 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
CNHFAHCC_04354 | 1.3e-48 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
CNHFAHCC_04355 | 1.7e-87 | yrvC | P | regulatory, ligand-binding protein related to C-terminal domains of K channels | ||
CNHFAHCC_04356 | 0.0 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
CNHFAHCC_04357 | 9.4e-49 | yrzD | S | Post-transcriptional regulator | ||
CNHFAHCC_04358 | 5.7e-270 | spoVB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
CNHFAHCC_04359 | 2.2e-114 | yrbG | S | membrane | ||
CNHFAHCC_04360 | 1.2e-74 | yrzE | S | Protein of unknown function (DUF3792) | ||
CNHFAHCC_04361 | 1.1e-38 | yajC | U | Preprotein translocase subunit YajC | ||
CNHFAHCC_04362 | 5.2e-228 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
CNHFAHCC_04363 | 2e-194 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
CNHFAHCC_04364 | 2.6e-18 | yrzS | S | Protein of unknown function (DUF2905) | ||
CNHFAHCC_04365 | 6.6e-187 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
CNHFAHCC_04366 | 1.6e-106 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
CNHFAHCC_04367 | 4.8e-93 | bofC | S | BofC C-terminal domain | ||
CNHFAHCC_04368 | 5.3e-253 | csbX | EGP | Major facilitator Superfamily | ||
CNHFAHCC_04369 | 1.3e-193 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
CNHFAHCC_04370 | 6.5e-119 | yrzF | T | serine threonine protein kinase | ||
CNHFAHCC_04372 | 2.4e-35 | S | Family of unknown function (DUF5412) | |||
CNHFAHCC_04374 | 1.8e-262 | alsT | E | Sodium alanine symporter | ||
CNHFAHCC_04375 | 1.9e-127 | yebC | K | transcriptional regulatory protein | ||
CNHFAHCC_04376 | 1e-46 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
CNHFAHCC_04377 | 9.8e-158 | safA | M | spore coat assembly protein SafA | ||
CNHFAHCC_04378 | 2.8e-215 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
CNHFAHCC_04379 | 5.4e-161 | nadC | 1.4.3.16, 2.4.2.19 | H | Belongs to the NadC ModD family | |
CNHFAHCC_04380 | 2.7e-307 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
CNHFAHCC_04381 | 1.2e-230 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
CNHFAHCC_04382 | 3.6e-94 | niaR | S | small molecule binding protein (contains 3H domain) | ||
CNHFAHCC_04383 | 3.3e-163 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
CNHFAHCC_04384 | 2.2e-73 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
CNHFAHCC_04385 | 1.5e-231 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
CNHFAHCC_04386 | 1.5e-106 | spo0B | T | Sporulation initiation phospho-transferase B, C-terminal | ||
CNHFAHCC_04387 | 2.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
CNHFAHCC_04388 | 4.1e-56 | ysxB | J | ribosomal protein | ||
CNHFAHCC_04389 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
CNHFAHCC_04390 | 9.2e-161 | spoIVFB | S | Stage IV sporulation protein | ||
CNHFAHCC_04391 | 3.8e-145 | spoIVFA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
CNHFAHCC_04392 | 2.5e-144 | minD | D | Belongs to the ParA family | ||
CNHFAHCC_04393 | 1.4e-108 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
CNHFAHCC_04394 | 1.4e-84 | mreD | M | shape-determining protein | ||
CNHFAHCC_04395 | 2.8e-157 | mreC | M | Involved in formation and maintenance of cell shape | ||
CNHFAHCC_04396 | 1.8e-184 | mreB | D | Rod shape-determining protein MreB | ||
CNHFAHCC_04397 | 2.1e-117 | radC | E | Belongs to the UPF0758 family | ||
CNHFAHCC_04398 | 2.8e-102 | maf | D | septum formation protein Maf | ||
CNHFAHCC_04399 | 1.1e-168 | spoIIB | S | Sporulation related domain | ||
CNHFAHCC_04400 | 6.6e-85 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
CNHFAHCC_04401 | 4.3e-247 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
CNHFAHCC_04402 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
CNHFAHCC_04403 | 1.6e-25 | |||||
CNHFAHCC_04404 | 1.5e-199 | ysxE | S | A protein kinase that phosphorylates Ser and Thr residues. Probably acts to suppress the effects of stress linked to accumulation of reactive oxygen species. Probably involved in the extracytoplasmic stress response | ||
CNHFAHCC_04405 | 1.9e-226 | spoVID | M | stage VI sporulation protein D | ||
CNHFAHCC_04406 | 4.6e-249 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
CNHFAHCC_04407 | 5.6e-183 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
CNHFAHCC_04408 | 4.4e-146 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
CNHFAHCC_04409 | 3e-173 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
CNHFAHCC_04410 | 3.6e-146 | hemX | O | cytochrome C | ||
CNHFAHCC_04411 | 3.5e-247 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
CNHFAHCC_04412 | 1.4e-89 | ysxD | ||||
CNHFAHCC_04413 | 1.2e-106 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
CNHFAHCC_04414 | 0.0 | lon | 3.4.21.53 | O | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner | |
CNHFAHCC_04415 | 2.3e-311 | lonB | 2.7.7.7, 3.4.21.53 | LO | Belongs to the peptidase S16 family | |
CNHFAHCC_04416 | 3.4e-233 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
CNHFAHCC_04417 | 8.3e-227 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
CNHFAHCC_04418 | 2.3e-187 | ysoA | H | Tetratricopeptide repeat | ||
CNHFAHCC_04419 | 8.1e-116 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
CNHFAHCC_04420 | 3.7e-48 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
CNHFAHCC_04421 | 4.1e-144 | ant | 2.7.7.47 | S | Domain of unknown function (DUF4111) | |
CNHFAHCC_04422 | 3.7e-62 | macB | V | MacB-like periplasmic core domain | ||
CNHFAHCC_04423 | 1.1e-70 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
CNHFAHCC_04424 | 6.2e-114 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
CNHFAHCC_04425 | 2.9e-235 | PT | Cyclic nucleotide-monophosphate binding domain | |||
CNHFAHCC_04426 | 2.8e-250 | S | Glycosyl hydrolase-like 10 | |||
CNHFAHCC_04427 | 2.8e-265 | cpgS | S | cyclic 2,3-diphosphoglycerate synthetase activity | ||
CNHFAHCC_04428 | 2e-174 | arcC | 2.7.2.2 | F | Belongs to the carbamate kinase family | |
CNHFAHCC_04429 | 5.5e-208 | nrdB | 1.17.4.1 | F | Ribonucleotide reductase, small chain | |
CNHFAHCC_04430 | 9e-142 | U | ABC-2 type transporter | |||
CNHFAHCC_04431 | 3.5e-140 | 3.6.3.38, 3.6.3.40 | GM | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_04432 | 1.2e-177 | M | RmlD substrate binding domain | |||
CNHFAHCC_04433 | 7.9e-126 | S | Protein of unknown function (DUF2993) | |||
CNHFAHCC_04434 | 1.7e-99 | S | Cofactor assembly of complex C subunit B | |||
CNHFAHCC_04435 | 1.7e-66 | |||||
CNHFAHCC_04436 | 2.9e-29 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_04437 | 9.6e-230 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
CNHFAHCC_04438 | 9.3e-53 | |||||
CNHFAHCC_04439 | 2.1e-145 | 3.1.3.18 | S | HAD-hyrolase-like | ||
CNHFAHCC_04440 | 8.9e-231 | argG | 6.3.4.5 | E | Arginosuccinate synthase | |
CNHFAHCC_04441 | 1e-195 | yjgB | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
CNHFAHCC_04442 | 9.3e-68 | S | Protein of unknown function (DUF1269) | |||
CNHFAHCC_04443 | 2.2e-129 | pilI | S | ABC-2 family transporter protein | ||
CNHFAHCC_04444 | 3.5e-182 | 2.1.1.10 | H | Homocysteine S-methyltransferase | ||
CNHFAHCC_04445 | 4.7e-112 | im30 | KT | PspA/IM30 family | ||
CNHFAHCC_04446 | 1.2e-178 | |||||
CNHFAHCC_04447 | 5.2e-75 | S | Predicted membrane protein (DUF2214) | |||
CNHFAHCC_04448 | 5.1e-101 | 1.10.9.1 | C | Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions | ||
CNHFAHCC_04449 | 3.2e-13 | S | Protein of unknown function (DUF2892) | |||
CNHFAHCC_04450 | 1.9e-86 | P | PFAM Rhodanese-like domain | |||
CNHFAHCC_04451 | 6.1e-108 | tehB | Q | Tellurite resistance protein TehB | ||
CNHFAHCC_04452 | 2.9e-98 | ste14 | O | Methyltransferase | ||
CNHFAHCC_04453 | 4.6e-210 | pufM | 1.10.3.9 | C | Photosystem II (PSII) is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1 D2 (PsbA PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors | |
CNHFAHCC_04454 | 1.4e-158 | surE | 3.1.3.5 | S | Nucleotidase that shows phosphatase activity on nucleoside 5'-monophosphates | |
CNHFAHCC_04455 | 3e-99 | S | Protein of unknown function (DUF3727) | |||
CNHFAHCC_04456 | 4.4e-200 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
CNHFAHCC_04457 | 4.6e-224 | anmK | 2.7.1.170, 4.2.1.126 | F | Catalyzes the specific phosphorylation of 1,6-anhydro-N- acetylmuramic acid (anhMurNAc) with the simultaneous cleavage of the 1,6-anhydro ring, generating MurNAc-6-P. Is required for the utilization of anhMurNAc either imported from the medium or derived from its own cell wall murein, and thus plays a role in cell wall recycling | |
CNHFAHCC_04458 | 1.8e-59 | T | Bacterial SH3 domain homologues | |||
CNHFAHCC_04459 | 2.1e-154 | ycgQ | S | TIGRFAM TIGR03943 family protein | ||
CNHFAHCC_04460 | 8.1e-246 | glgC | 2.7.7.27, 3.2.1.68 | CBM48,GH13 | F | Nucleotidyl transferase |
CNHFAHCC_04461 | 0.0 | htpG | O | Hsp90 protein | ||
CNHFAHCC_04462 | 4.6e-99 | L | DDE superfamily endonuclease | |||
CNHFAHCC_04463 | 1.3e-31 | L | transposition | |||
CNHFAHCC_04464 | 4.6e-157 | L | Transposase | |||
CNHFAHCC_04465 | 2.2e-84 | L | DDE superfamily endonuclease | |||
CNHFAHCC_04467 | 1.3e-280 | 3.4.24.3 | O | Subtilase family | ||
CNHFAHCC_04468 | 1.1e-115 | pgp | 3.1.3.18 | S | Haloacid dehalogenase-like hydrolase | |
CNHFAHCC_04469 | 8.8e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
CNHFAHCC_04470 | 5.4e-54 | |||||
CNHFAHCC_04471 | 2.2e-67 | S | COGs COG3937 conserved | |||
CNHFAHCC_04472 | 0.0 | V | Protein export membrane protein | |||
CNHFAHCC_04473 | 1.3e-84 | S | Polyketide cyclase / dehydrase and lipid transport | |||
CNHFAHCC_04474 | 6.5e-38 | |||||
CNHFAHCC_04475 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | XFP C-terminal domain | |
CNHFAHCC_04476 | 0.0 | ilvD | 4.2.1.9 | E | Dehydratase family | |
CNHFAHCC_04477 | 3.3e-255 | 2.7.7.7 | L | GIY-YIG catalytic domain | ||
CNHFAHCC_04478 | 5e-54 | T | ATPase activity | |||
CNHFAHCC_04479 | 0.0 | helY | L | DSHCT | ||
CNHFAHCC_04480 | 5.8e-255 | |||||
CNHFAHCC_04481 | 6.7e-87 | |||||
CNHFAHCC_04482 | 9.5e-291 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
CNHFAHCC_04483 | 0.0 | ftsA | D | cell division | ||
CNHFAHCC_04485 | 1.1e-206 | |||||
CNHFAHCC_04486 | 1.7e-215 | 3.4.21.107 | S | Wd-40 repeat | ||
CNHFAHCC_04487 | 1.5e-129 | fnr-1 | K | cyclic nucleotide-binding | ||
CNHFAHCC_04488 | 0.0 | norB | 1.7.2.5 | P | PFAM Cytochrome C and Quinol oxidase polypeptide I | |
CNHFAHCC_04489 | 8e-87 | elaA | K | protein acetylation | ||
CNHFAHCC_04490 | 9e-135 | S | Protein of unknown function (DUF2887) | |||
CNHFAHCC_04492 | 5.9e-26 | |||||
CNHFAHCC_04493 | 2e-146 | NU | Pili and flagellar-assembly chaperone, PapD N-terminal domain | |||
CNHFAHCC_04494 | 4.3e-92 | |||||
CNHFAHCC_04495 | 5.1e-75 | G | Toxic component of a toxin-antitoxin (TA) module. An RNase | |||
CNHFAHCC_04497 | 1.6e-25 | K | Transcriptional regulator | |||
CNHFAHCC_04498 | 2.5e-121 | KT | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_04499 | 6.9e-37 | |||||
CNHFAHCC_04500 | 4e-220 | degT | M | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
CNHFAHCC_04501 | 5.6e-163 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
CNHFAHCC_04502 | 0.0 | P | PFAM TrkA-N domain | |||
CNHFAHCC_04503 | 1.6e-135 | gst1 | 2.5.1.18 | O | Glutathione S-transferase, N-terminal domain | |
CNHFAHCC_04504 | 0.0 | U | Haemolysin secretion/activation protein ShlB/FhaC/HecB | |||
CNHFAHCC_04505 | 4.2e-308 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
CNHFAHCC_04506 | 3.3e-77 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
CNHFAHCC_04507 | 1.9e-106 | S | Protein of unknown function (DUF3172) | |||
CNHFAHCC_04508 | 5.4e-56 | S | COGs COG5439 conserved | |||
CNHFAHCC_04509 | 1.9e-112 | S | COGs COG5381 conserved | |||
CNHFAHCC_04510 | 2e-152 | T | diguanylate cyclase | |||
CNHFAHCC_04511 | 2.1e-199 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
CNHFAHCC_04512 | 9.7e-16 | psaI | U | May help in the organization of the PsaL subunit | ||
CNHFAHCC_04513 | 6.5e-84 | psaL | U | Photosystem I reaction centre subunit XI | ||
CNHFAHCC_04514 | 2.9e-136 | G | Histidine phosphatase superfamily (branch 1) | |||
CNHFAHCC_04515 | 0.0 | M | Carbohydrate-selective porin, OprB family | |||
CNHFAHCC_04516 | 1.8e-239 | ama | S | Peptidase dimerisation domain | ||
CNHFAHCC_04517 | 1.6e-123 | sec59 | 2.7.1.182 | I | Dolichol kinase | |
CNHFAHCC_04518 | 0.0 | comA | V | Peptidase C39 family | ||
CNHFAHCC_04521 | 9.2e-172 | K | PFAM Acetyltransferase (GNAT) family | |||
CNHFAHCC_04522 | 1.2e-79 | O | COG2994 ACP hemolysin acyltransferase (hemolysin-activating protein) | |||
CNHFAHCC_04523 | 0.0 | cloSI | 3.4.22.8 | Q | Haemolysin-type calcium-binding repeat (2 copies) | |
CNHFAHCC_04524 | 1.3e-111 | |||||
CNHFAHCC_04525 | 0.0 | 3.4.24.40 | Q | calcium- and calmodulin-responsive adenylate cyclase activity | ||
CNHFAHCC_04526 | 1.1e-294 | kaiC | T | Core component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. Binds to DNA. The KaiABC complex may act as a promoter-nonspecific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction | ||
CNHFAHCC_04527 | 3.1e-50 | kaiB | T | Component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. The KaiABC complex may act as a promoter-non-specific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction. In the complex, it decreases the phosphorylation status of KaiC. It has no effect on KaiC by itself, but instead needs the presence of both KaiA and KaiC, suggesting that it acts by antagonizing the interaction between KaiA and KaiC | ||
CNHFAHCC_04528 | 8.6e-170 | kaiA | J | Component of the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria. The KaiABC complex may act as a promoter-nonspecific transcription regulator that represses transcription, possibly by acting on the state of chromosome compaction. In the complex, it enhances the phosphorylation status of KaiC. In contrast, the presence of KaiB in the complex decreases the phosphorylation status of KaiC, suggesting that KaiB acts by antagonizing the interaction between KaiA and KaiC. A KaiA dimer is sufficient to enhance KaiC hexamer phosphorylation | ||
CNHFAHCC_04529 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, C-terminal domain | |
CNHFAHCC_04530 | 0.0 | S | COGs COG5305 membrane protein | |||
CNHFAHCC_04531 | 5.8e-22 | N | HicA toxin of bacterial toxin-antitoxin, | |||
CNHFAHCC_04532 | 1.4e-30 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_04533 | 1.3e-102 | MA20_36560 | S | NYN domain | ||
CNHFAHCC_04534 | 8.8e-43 | S | Domain of unknown function (DUF4327) | |||
CNHFAHCC_04535 | 7.2e-27 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_04536 | 9.5e-25 | N | PFAM YcfA-like protein | |||
CNHFAHCC_04537 | 3.7e-182 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
CNHFAHCC_04538 | 4.7e-165 | dmnB | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
CNHFAHCC_04539 | 6.5e-22 | |||||
CNHFAHCC_04540 | 7.2e-237 | U | Arsenical pump membrane protein | |||
CNHFAHCC_04541 | 2.9e-87 | 4.2.1.1 | P | reversible hydration of carbon dioxide | ||
CNHFAHCC_04542 | 4.6e-241 | eno | 4.2.1.11 | F | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
CNHFAHCC_04543 | 2.5e-42 | S | Tetratricopeptide repeat | |||
CNHFAHCC_04544 | 5e-78 | S | Domain of unknown function (DUF4278) | |||
CNHFAHCC_04545 | 1e-278 | chlN | 1.3.7.7 | F | Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The NB-protein (ChlN-ChlB) is the catalytic component of the complex | |
CNHFAHCC_04546 | 3.4e-163 | chlL | 1.3.7.7 | F | Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The L component serves as a unique electron donor to the NB-component of the complex, and binds Mg-ATP | |
CNHFAHCC_04547 | 1.8e-127 | S | Alternative locus ID | |||
CNHFAHCC_04548 | 2.2e-311 | 2.4.1.18 | GH57 | G | Domain of unknown function (DUF1957) | |
CNHFAHCC_04549 | 1.4e-244 | S | Glycosyl hydrolase-like 10 | |||
CNHFAHCC_04550 | 1.3e-204 | ugpC | E | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_04551 | 2.3e-245 | stpA | 3.1.3.69 | F | Glucosylglycerol-phosphate phosphatase (Salt_tol_Pase) | |
CNHFAHCC_04552 | 1.4e-242 | yhjK | T | Putative diguanylate phosphodiesterase | ||
CNHFAHCC_04553 | 3.9e-270 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
CNHFAHCC_04554 | 1.6e-64 | L | Transposase | |||
CNHFAHCC_04555 | 2.4e-62 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_04556 | 9.8e-129 | KT | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_04557 | 1.2e-137 | cpcG2 | 2.7.7.24 | G | Phycobilisome Linker polypeptide | |
CNHFAHCC_04559 | 2.6e-269 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |||
CNHFAHCC_04560 | 8.4e-190 | L | PFAM Transposase | |||
CNHFAHCC_04561 | 1.8e-164 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_04562 | 1e-60 | S | Domain of unknown function (DUF1815) | |||
CNHFAHCC_04563 | 0.0 | S | CAAX protease self-immunity | |||
CNHFAHCC_04564 | 1.7e-136 | pgl | 2.7.1.12, 3.1.1.31 | F | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
CNHFAHCC_04565 | 1.5e-234 | devB | M | Biotin-lipoyl like | ||
CNHFAHCC_04566 | 1.5e-214 | devC | V | FtsX-like permease family | ||
CNHFAHCC_04567 | 3.6e-86 | M | Four repeated domains in the Fasciclin I family of proteins, present in many other contexts. | |||
CNHFAHCC_04568 | 4.1e-278 | ndbC | 1.6.99.3 | C | Pyridine nucleotide-disulphide oxidoreductase | |
CNHFAHCC_04569 | 2.6e-88 | S | Predicted membrane protein (DUF2231) | |||
CNHFAHCC_04570 | 1.8e-118 | S | Predicted membrane protein (DUF2231) | |||
CNHFAHCC_04572 | 0.0 | M | Protein of unknown function (DUF3352) | |||
CNHFAHCC_04573 | 2.4e-81 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
CNHFAHCC_04574 | 5.4e-50 | |||||
CNHFAHCC_04575 | 4.2e-267 | MT | Cyclic nucleotide-monophosphate binding domain | |||
CNHFAHCC_04576 | 7.3e-40 | NPD7_560 | S | Domain of unknown function (DUF370) | ||
CNHFAHCC_04577 | 7.6e-154 | yfiH | S | Multi-copper polyphenol oxidoreductase laccase | ||
CNHFAHCC_04578 | 1.8e-161 | S | Mitochondrial biogenesis AIM24 | |||
CNHFAHCC_04579 | 3.7e-125 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
CNHFAHCC_04580 | 9.9e-123 | S | Mitochondrial biogenesis AIM24 | |||
CNHFAHCC_04581 | 3.2e-97 | M | Peptidase family M23 | |||
CNHFAHCC_04582 | 2.5e-144 | cpmA | S | AIR carboxylase | ||
CNHFAHCC_04583 | 1.2e-78 | |||||
CNHFAHCC_04584 | 0.0 | susD | M | Has lipid A 3-O-deacylase activity. Hydrolyzes the ester bond at the 3 position of lipid A, a bioactive component of lipopolysaccharide (LPS), thereby releasing the primary fatty acyl moiety | ||
CNHFAHCC_04585 | 1.6e-130 | S | Anaphase-promoting complex subunit 4 WD40 domain | |||
CNHFAHCC_04586 | 2.3e-215 | 2.4.1.83, 2.7.8.12 | GT2 | M | Glycosyl transferase family 21 | |
CNHFAHCC_04587 | 2.1e-60 | iscA | S | Iron-sulphur cluster biosynthesis | ||
CNHFAHCC_04588 | 3.5e-143 | sigF | K | Sigma-70, region 4 | ||
CNHFAHCC_04589 | 6.1e-176 | yniA | G | Fructosamine kinase | ||
CNHFAHCC_04590 | 1.6e-60 | grxC | O | Has a glutathione-disulfide oxidoreductase activity in the presence of NADPH and glutathione reductase. Reduces low molecular weight disulfides and proteins | ||
CNHFAHCC_04591 | 5.6e-233 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
CNHFAHCC_04592 | 4.9e-162 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
CNHFAHCC_04594 | 9.5e-233 | lhgO | 1.1.99.2 | S | FAD dependent oxidoreductase | |
CNHFAHCC_04595 | 0.0 | mpg | 1.6.5.5, 2.7.7.13, 5.4.2.10, 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
CNHFAHCC_04596 | 1.2e-181 | K | sequence-specific DNA binding | |||
CNHFAHCC_04597 | 5.7e-252 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthase small chain, CPSase domain | |
CNHFAHCC_04598 | 2.9e-190 | ldhA | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
CNHFAHCC_04599 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | GXGXG motif | |
CNHFAHCC_04600 | 5.8e-21 | yqjG | 1.8.5.7, 2.5.1.18 | O | Glutathione S-transferase, C-terminal domain | |
CNHFAHCC_04601 | 1.1e-95 | |||||
CNHFAHCC_04602 | 2e-94 | |||||
CNHFAHCC_04604 | 7.2e-155 | |||||
CNHFAHCC_04605 | 0.0 | acnB | 4.2.1.3, 4.2.1.99 | C | Aconitate B N-terminal domain | |
CNHFAHCC_04606 | 3.2e-59 | DJ | Cytotoxic translational repressor of toxin-antitoxin stability system | |||
CNHFAHCC_04607 | 3.1e-40 | S | InterPro IPR007367 | |||
CNHFAHCC_04608 | 5.2e-128 | ccdA | O | Cytochrome C biogenesis protein transmembrane region | ||
CNHFAHCC_04609 | 3e-181 | nadA | 2.5.1.72 | F | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
CNHFAHCC_04610 | 3e-102 | |||||
CNHFAHCC_04611 | 0.0 | speA | 4.1.1.19 | E | Catalyzes the biosynthesis of agmatine from arginine | |
CNHFAHCC_04612 | 4.7e-54 | S | PFAM PilT protein domain protein | |||
CNHFAHCC_04613 | 4.1e-29 | K | protein encoded in hypervariable junctions of pilus gene clusters | |||
CNHFAHCC_04614 | 2.7e-131 | S | Methyltransferase domain | |||
CNHFAHCC_04615 | 4.1e-302 | invA | 3.2.1.26 | GH32 | G | Alkaline and neutral invertase |
CNHFAHCC_04616 | 3.8e-137 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
CNHFAHCC_04617 | 0.0 | prlC | 3.4.24.70 | E | Peptidase family M3 | |
CNHFAHCC_04618 | 1.8e-189 | S | TIR domain | |||
CNHFAHCC_04619 | 0.0 | lysC | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
CNHFAHCC_04621 | 1.1e-244 | MA20_36195 | S | Peptidogalycan biosysnthesis/recognition | ||
CNHFAHCC_04622 | 6.2e-107 | S | Domain of unknown function (DUF427) | |||
CNHFAHCC_04623 | 8.7e-147 | |||||
CNHFAHCC_04624 | 7.9e-75 | ble | E | Glyoxalase-like domain | ||
CNHFAHCC_04625 | 1.5e-73 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
CNHFAHCC_04626 | 1.4e-63 | psaK2 | U | Photosystem I psaG / psaK | ||
CNHFAHCC_04627 | 8.9e-80 | |||||
CNHFAHCC_04628 | 0.0 | nadB | 1.3.5.1, 1.3.5.4, 1.4.3.16 | F | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
CNHFAHCC_04629 | 1.1e-141 | hisA | 5.3.1.16 | E | Histidine biosynthesis protein | |
CNHFAHCC_04630 | 1.5e-67 | H | Domain of unknown function (DUF4346) | |||
CNHFAHCC_04631 | 4.4e-183 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
CNHFAHCC_04632 | 1.8e-34 | nifU | O | NifU-like domain | ||
CNHFAHCC_04634 | 1.1e-149 | C | Radical SAM | |||
CNHFAHCC_04635 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
CNHFAHCC_04636 | 9.8e-284 | mglA | S | Domain of unknown function (DUF697) | ||
CNHFAHCC_04637 | 0.0 | pkn5 | 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
CNHFAHCC_04638 | 1.3e-105 | SEN0012 | S | Rhomboid family | ||
CNHFAHCC_04639 | 0.0 | helZ | 2.7.11.1 | KL | SNF2 Helicase protein | |
CNHFAHCC_04640 | 1.8e-87 | apcF | C | Phycobilisome protein | ||
CNHFAHCC_04641 | 1.2e-219 | chrA | P | Chromate transporter | ||
CNHFAHCC_04642 | 6.7e-98 | U | Prokaryotic N-terminal methylation motif | |||
CNHFAHCC_04643 | 4e-198 | cysA | 3.6.3.25, 3.6.3.29 | P | Part of the ABC transporter complex CysAWTP involved in sulfate thiosulfate import. Responsible for energy coupling to the transport system | |
CNHFAHCC_04644 | 5.5e-147 | cysW | P | Sulfate transport system permease protein CysW | ||
CNHFAHCC_04645 | 4.9e-122 | cysT | O | Sulfate transport system permease protein CysT | ||
CNHFAHCC_04646 | 1.3e-45 | P | NIL | |||
CNHFAHCC_04647 | 1.2e-175 | subI | P | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_04648 | 1.5e-147 | T | - Catabolite gene activator and regulatory subunit of cAMP-dependent protein | |||
CNHFAHCC_04649 | 1.1e-147 | |||||
CNHFAHCC_04650 | 6.8e-158 | 3.1.3.25 | G | Inositol monophosphatase family | ||
CNHFAHCC_04651 | 1e-139 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_04652 | 2.6e-277 | flgE | N | Protein of unknown function (DUF3370) | ||
CNHFAHCC_04653 | 8.6e-133 | |||||
CNHFAHCC_04655 | 1.1e-164 | S | SWIM zinc finger | |||
CNHFAHCC_04656 | 2.5e-294 | 2.7.13.3 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | ||
CNHFAHCC_04657 | 0.0 | S | Gtr1/RagA G protein conserved region | |||
CNHFAHCC_04658 | 0.0 | 2.6.1.13 | E | Amidinotransferase | ||
CNHFAHCC_04659 | 4.1e-93 | |||||
CNHFAHCC_04660 | 6.3e-128 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
CNHFAHCC_04661 | 5.9e-44 | S | Protein of unknown function (DUF3146) | |||
CNHFAHCC_04662 | 2.7e-82 | bfrA | 1.16.3.1 | P | Iron-storage protein, whose ferroxidase center binds Fe(2 ) ions, oxidizes them by dioxygen to Fe(3 ), and participates in the subsequent Fe(3 ) oxide mineral core formation within the central cavity of the protein complex | |
CNHFAHCC_04663 | 1.6e-63 | |||||
CNHFAHCC_04664 | 1.6e-182 | murB | 1.3.1.98 | M | UDP-N-acetylenolpyruvoylglucosamine reductase, C-terminal domain | |
CNHFAHCC_04665 | 1.6e-293 | murC | 6.3.2.8 | M | Mur ligase family, catalytic domain | |
CNHFAHCC_04666 | 5.8e-191 | gapB | 1.2.1.12, 1.2.1.59 | F | Glyceraldehyde 3-phosphate dehydrogenase, NAD binding domain | |
CNHFAHCC_04667 | 0.0 | pepN | 3.4.11.2 | CE | Peptidase family M1 domain | |
CNHFAHCC_04668 | 6.9e-127 | M | heme binding | |||
CNHFAHCC_04669 | 3e-28 | |||||
CNHFAHCC_04670 | 1.9e-55 | S | Domain of unknown function (DUF4258) | |||
CNHFAHCC_04671 | 5.5e-24 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_04672 | 8.8e-245 | xylB | 2.7.1.17 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
CNHFAHCC_04673 | 8.5e-78 | sufE | S | Fe-S metabolism associated domain | ||
CNHFAHCC_04674 | 1.1e-222 | pyrD | 1.3.1.14, 1.3.5.2 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
CNHFAHCC_04675 | 3.9e-204 | nuoH | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient | |
CNHFAHCC_04677 | 3.3e-90 | ndhI | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient | |
CNHFAHCC_04678 | 1.2e-95 | ndhG | 1.6.5.3 | C | NADH-ubiquinone/plastoquinone oxidoreductase chain 6 | |
CNHFAHCC_04679 | 4.2e-47 | nuoK | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_04680 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
CNHFAHCC_04681 | 4.3e-258 | S | FIST N domain | |||
CNHFAHCC_04682 | 1e-37 | D | positive regulation of growth | |||
CNHFAHCC_04683 | 5.8e-42 | S | PIN domain | |||
CNHFAHCC_04684 | 8.9e-116 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
CNHFAHCC_04685 | 8.6e-204 | VVA0737 | S | Peptidase family M50 | ||
CNHFAHCC_04686 | 0.0 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |||
CNHFAHCC_04687 | 0.0 | KL | Domain of unknown function (DUF3854) | |||
CNHFAHCC_04688 | 5.7e-109 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18, 5.4.99.23 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
CNHFAHCC_04689 | 1.6e-134 | |||||
CNHFAHCC_04690 | 0.0 | rnj | J | activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
CNHFAHCC_04691 | 1.3e-170 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
CNHFAHCC_04692 | 5e-182 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
CNHFAHCC_04693 | 1.2e-253 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
CNHFAHCC_04694 | 3.5e-123 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
CNHFAHCC_04695 | 2.4e-253 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
CNHFAHCC_04696 | 4.3e-195 | U | Ion channel | |||
CNHFAHCC_04697 | 6.3e-182 | U | Ammonium Transporter Family | |||
CNHFAHCC_04698 | 2e-112 | U | Ammonium Transporter Family | |||
CNHFAHCC_04699 | 2.6e-158 | trpC | 4.1.1.48, 5.3.1.24 | E | Indole-3-glycerol phosphate synthase | |
CNHFAHCC_04700 | 1.6e-168 | cysQ | 3.1.3.7 | P | Inositol monophosphatase family | |
CNHFAHCC_04701 | 4.9e-90 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
CNHFAHCC_04702 | 5.2e-180 | dnaJ | A | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
CNHFAHCC_04703 | 2.8e-41 | tusA | 1.8.7.1 | O | Sulfurtransferase TusA | |
CNHFAHCC_04704 | 6.3e-215 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
CNHFAHCC_04705 | 2.7e-41 | S | Domain of unknown function (DUF4327) | |||
CNHFAHCC_04706 | 1.4e-235 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
CNHFAHCC_04707 | 3.8e-116 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
CNHFAHCC_04708 | 1.8e-41 | S | Uncharacterized protein family UPF0016 | |||
CNHFAHCC_04709 | 2.3e-256 | MA20_41470 | S | Protein of unknown function (DUF815) | ||
CNHFAHCC_04710 | 2.7e-103 | D | AAA domain | |||
CNHFAHCC_04711 | 5e-209 | psbD | 1.10.3.9 | C | Photosystem II (PSII) is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1 D2 (PsbA PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors. D2 is needed for assembly of a stable PSII complex | |
CNHFAHCC_04712 | 1.4e-161 | ubiA | 2.5.1.39 | H | Catalyzes the prenylation of para-hydroxybenzoate (PHB) with an all-trans polyprenyl group. Mediates the second step in the final reaction sequence of plastoquinone-9 (PQ-9) biosynthesis, which is the condensation of the polyisoprenoid side chain with PHB, generating the first membrane-bound Q intermediate 4-hydroxy-3-solanesylbenzoate | |
CNHFAHCC_04713 | 4.3e-67 | ssb | L | Single-strand binding protein family | ||
CNHFAHCC_04714 | 1.7e-88 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
CNHFAHCC_04715 | 2.8e-171 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
CNHFAHCC_04716 | 1.1e-124 | trkA | P | TrkA-C domain | ||
CNHFAHCC_04717 | 2e-167 | |||||
CNHFAHCC_04719 | 3e-08 | |||||
CNHFAHCC_04720 | 1.2e-304 | asnS | 6.1.1.22 | J | tRNA synthetases class II (D, K and N) | |
CNHFAHCC_04721 | 4.4e-222 | lptG | S | Predicted permease YjgP/YjgQ family | ||
CNHFAHCC_04722 | 1.5e-180 | tas | 1.1.1.65 | C | Aldo/keto reductase family | |
CNHFAHCC_04723 | 1.1e-160 | S | Domain of unknown function (DUF3598) | |||
CNHFAHCC_04724 | 2.4e-80 | S | TM2 domain | |||
CNHFAHCC_04725 | 2.2e-145 | salX | V | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_04726 | 1.8e-285 | S | CHAT domain | |||
CNHFAHCC_04727 | 8.3e-240 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
CNHFAHCC_04728 | 2.6e-106 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
CNHFAHCC_04729 | 4.6e-134 | F | Peptidase C26 | |||
CNHFAHCC_04730 | 2e-180 | gtrB | GT2 | M | Glycosyltransferase like family 2 | |
CNHFAHCC_04731 | 0.0 | argS | 6.1.1.19 | J | Arginyl tRNA synthetase N terminal dom | |
CNHFAHCC_04732 | 1.6e-250 | mglA | S | Domain of unknown function (DUF697) | ||
CNHFAHCC_04733 | 1.4e-272 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
CNHFAHCC_04734 | 6.3e-160 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
CNHFAHCC_04735 | 1.4e-141 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
CNHFAHCC_04736 | 3e-215 | corA | P | Mediates influx of magnesium ions | ||
CNHFAHCC_04737 | 5.1e-187 | pfkB | 2.7.1.15, 2.7.1.4 | G | pfkB family carbohydrate kinase | |
CNHFAHCC_04738 | 1.1e-92 | |||||
CNHFAHCC_04739 | 2.2e-173 | apa2 | 2.7.7.53 | F | ATP adenylyltransferase | |
CNHFAHCC_04740 | 7.6e-202 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
CNHFAHCC_04741 | 0.0 | O | Subtilase family | |||
CNHFAHCC_04742 | 0.0 | slt | GH23 | M | Transglycosylase SLT domain | |
CNHFAHCC_04743 | 3.9e-204 | tcsS4 | 2.7.13.3 | T | HAMP domain | |
CNHFAHCC_04744 | 1.3e-153 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
CNHFAHCC_04745 | 7e-164 | aglG | P | ABC-type sugar transport system, permease component | ||
CNHFAHCC_04746 | 3.7e-150 | G | COG1175 ABC-type sugar transport systems permease components | |||
CNHFAHCC_04747 | 2.8e-251 | aglE | G | ABC-type sugar transport system periplasmic component | ||
CNHFAHCC_04748 | 0.0 | ysh1 | J | Zn-dependent metallo-hydrolase RNA specificity domain | ||
CNHFAHCC_04749 | 2.9e-295 | murE | 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
CNHFAHCC_04750 | 5.7e-129 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
CNHFAHCC_04751 | 1.9e-141 | panB | 2.1.2.11 | H | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate | |
CNHFAHCC_04752 | 3.1e-127 | chlM | 2.1.1.11 | H | Magnesium-protoporphyrin IX methyltransferase C-terminus | |
CNHFAHCC_04753 | 7.5e-49 | rbpD | S | Pfam:RRM_6 | ||
CNHFAHCC_04754 | 3.1e-199 | |||||
CNHFAHCC_04755 | 0.0 | ndhF4 | 1.6.5.3 | CP | NADH-Ubiquinone oxidoreductase (complex I), chain 5 N-terminus | |
CNHFAHCC_04756 | 1.6e-272 | nuoM | 1.6.5.3 | C | Proton-conducting membrane transporter | |
CNHFAHCC_04757 | 1.4e-158 | nasD | 3.6.3.36 | P | ATPases associated with a variety of cellular activities | |
CNHFAHCC_04758 | 0.0 | nasD | 3.6.3.36 | P | NMT1-like family | |
CNHFAHCC_04759 | 0.0 | M | Carbohydrate-selective porin, OprB family | |||
CNHFAHCC_04760 | 4e-153 | cmpB | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_04761 | 6.9e-272 | cmpA | P | NMT1-like family | ||
CNHFAHCC_04762 | 2.2e-165 | cmpR | K | LysR substrate binding domain | ||
CNHFAHCC_04763 | 1e-193 | pta | C | DRTGG domain | ||
CNHFAHCC_04764 | 5e-69 | |||||
CNHFAHCC_04765 | 3.2e-225 | ldpA | C | Iron-Sulfur binding protein C terminal | ||
CNHFAHCC_04766 | 8.4e-303 | crtH | 5.2.1.13 | Q | Flavin containing amine oxidoreductase | |
CNHFAHCC_04767 | 2e-114 | yodJ | 3.4.13.22, 3.4.16.4, 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
CNHFAHCC_04768 | 3.7e-221 | aspC4 | 4.1.1.82 | E | Cys/Met metabolism PLP-dependent enzyme | |
CNHFAHCC_04769 | 3.1e-237 | mgsA | 4.2.3.3 | GI | Diacylglycerol kinase catalytic domain (presumed) | |
CNHFAHCC_04771 | 5.5e-181 | cbiX | 4.99.1.3, 4.99.1.4, 5.4.99.60, 5.4.99.61 | H | CbiX | |
CNHFAHCC_04772 | 1.3e-51 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
CNHFAHCC_04773 | 1.2e-174 | ilvE | 2.6.1.42 | E | Belongs to the class-IV pyridoxal-phosphate-dependent aminotransferase family | |
CNHFAHCC_04774 | 0.0 | S | M61 glycyl aminopeptidase | |||
CNHFAHCC_04775 | 1.5e-225 | cheV | T | cheY-homologous receiver domain | ||
CNHFAHCC_04776 | 7.6e-61 | KT | cheY-homologous receiver domain | |||
CNHFAHCC_04777 | 4.5e-103 | cheW | NT | Two component signalling adaptor domain | ||
CNHFAHCC_04778 | 0.0 | T | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |||
CNHFAHCC_04779 | 2.7e-77 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |||
CNHFAHCC_04780 | 0.0 | pilL | 2.7.13.3 | T | Signal transducing histidine kinase, homodimeric domain | |
CNHFAHCC_04781 | 5.1e-84 | NT | Two component signalling adaptor domain | |||
CNHFAHCC_04782 | 4.8e-102 | |||||
CNHFAHCC_04783 | 0.0 | sps | 2.4.1.14, 2.4.1.246, 3.1.3.24, 3.1.3.79 | GT4 | M | Sucrose synthase |
CNHFAHCC_04784 | 1.4e-73 | S | Putative zinc- or iron-chelating domain | |||
CNHFAHCC_04785 | 1.4e-31 | ycf12 | U | A core subunit of photosystem II (PSII) | ||
CNHFAHCC_04786 | 1.5e-177 | T | diguanylate cyclase | |||
CNHFAHCC_04787 | 0.0 | M | O-Antigen ligase | |||
CNHFAHCC_04788 | 8.9e-142 | modA | P | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_04789 | 0.0 | modB | 3.6.3.25, 3.6.3.29 | P | Binding-protein-dependent transport system inner membrane component | |
CNHFAHCC_04790 | 7.8e-108 | S | Putative restriction endonuclease | |||
CNHFAHCC_04791 | 0.0 | nifJ | 1.2.7.1 | C | Oxidoreductase required for the transfer of electrons from pyruvate to flavodoxin | |
CNHFAHCC_04792 | 2.3e-78 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_04793 | 3.1e-89 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_04794 | 9.5e-197 | 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | ||
CNHFAHCC_04795 | 7.3e-222 | pfkA | 2.7.1.11, 2.7.1.90 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
CNHFAHCC_04796 | 0.0 | ybiO | M | Mechanosensitive ion channel | ||
CNHFAHCC_04797 | 3.6e-202 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
CNHFAHCC_04798 | 5.2e-40 | S | Uncharacterised protein family (UPF0175) | |||
CNHFAHCC_04799 | 4.1e-81 | S | Domain of unknown function (DUF3368) | |||
CNHFAHCC_04800 | 2.8e-309 | 5.5.1.19 | C | oxidoreductase | ||
CNHFAHCC_04801 | 2.7e-221 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
CNHFAHCC_04803 | 2e-194 | pdxA | 1.1.1.262, 1.1.1.408, 1.1.1.409 | H | Catalyzes the NAD(P)-dependent oxidation of 4- (phosphohydroxy)-L-threonine (HTP) into 2-amino-3-oxo-4- (phosphohydroxy)butyric acid which spontaneously decarboxylates to form 3-amino-2-oxopropyl phosphate (AHAP) | |
CNHFAHCC_04804 | 1.2e-32 | S | Protein of unknown function (DUF2997) | |||
CNHFAHCC_04805 | 2.6e-67 | ycf35 | S | Protein of unknown function (DUF1257) | ||
CNHFAHCC_04806 | 5.2e-66 | fer | C | 4Fe-4S single cluster domain of Ferredoxin I | ||
CNHFAHCC_04807 | 6e-177 | mprF | 2.3.2.3 | S | Lysylphosphatidylglycerol synthase TM region | |
CNHFAHCC_04808 | 4.3e-76 | queF | 1.7.1.13 | F | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
CNHFAHCC_04809 | 2.7e-249 | gdhA | 1.4.1.2, 1.4.1.3, 1.4.1.4 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
CNHFAHCC_04810 | 4.6e-67 | tdcF | 3.5.99.10 | J | Endoribonuclease L-PSP | |
CNHFAHCC_04811 | 3.7e-168 | yurQ | 2.7.7.7 | L | Excinuclease ABC C subunit | |
CNHFAHCC_04812 | 1.2e-63 | L | Putative transposase of IS4/5 family (DUF4096) | |||
CNHFAHCC_04813 | 5.1e-77 | L | Transposase | |||
CNHFAHCC_04814 | 5.4e-121 | L | DDE superfamily endonuclease | |||
CNHFAHCC_04815 | 1.4e-68 | L | transposition | |||
CNHFAHCC_04816 | 2.2e-229 | |||||
CNHFAHCC_04817 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits | |
CNHFAHCC_04819 | 4.7e-96 | enhA_2 | S | ErfK YbiS YcfS YnhG family protein | ||
CNHFAHCC_04820 | 1.5e-222 | corA | P | Mediates influx of magnesium ions | ||
CNHFAHCC_04821 | 0.0 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | ||
CNHFAHCC_04822 | 1e-72 | L | DDE superfamily endonuclease | |||
CNHFAHCC_04823 | 6e-157 | L | Transposase | |||
CNHFAHCC_04824 | 3.6e-156 | L | Transposase | |||
CNHFAHCC_04825 | 7.2e-46 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_04826 | 4.6e-102 | S | GXWXG protein | |||
CNHFAHCC_04827 | 3.6e-156 | L | Transposase | |||
CNHFAHCC_04828 | 1.1e-72 | I | Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA | |||
CNHFAHCC_04829 | 2.6e-225 | |||||
CNHFAHCC_04830 | 2.7e-70 | K | helix_turn_helix, mercury resistance | |||
CNHFAHCC_04831 | 2.8e-241 | E | Amino acid permease | |||
CNHFAHCC_04833 | 1e-86 | cyaA | 4.6.1.1 | S | CYTH | |
CNHFAHCC_04834 | 0.0 | hyuB | 3.5.2.14, 3.5.2.9 | EQ | Hydantoinase B/oxoprolinase | |
CNHFAHCC_04835 | 1.6e-21 | S | Proteolipid membrane potential modulator | |||
CNHFAHCC_04839 | 1.1e-225 | lptA | 3.5.1.28 | KLT | RIO1 family | |
CNHFAHCC_04840 | 6.9e-167 | yodJ | 3.4.13.22, 3.4.16.4, 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
CNHFAHCC_04841 | 0.0 | V | ABC-type multidrug transport system ATPase component | |||
CNHFAHCC_04842 | 0.0 | 2.7.11.1 | KT | diguanylate cyclase | ||
CNHFAHCC_04844 | 5.1e-89 | MA20_04335 | S | Protein of unknown function (DUF1348) | ||
CNHFAHCC_04845 | 5.9e-205 | KT | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_04846 | 5.2e-250 | P | Flavin-binding monooxygenase-like | |||
CNHFAHCC_04847 | 4e-89 | S | TIGRFAM MSMEG_0572 family protein | |||
CNHFAHCC_04848 | 1.1e-197 | nitA | 3.5.5.1, 3.5.5.7 | S | Carbon-nitrogen hydrolase | |
CNHFAHCC_04849 | 1e-204 | 1.17.98.2 | S | Elongator protein 3, MiaB family, Radical SAM | ||
CNHFAHCC_04850 | 8.6e-98 | K | Acetyltransferase (GNAT) family | |||
CNHFAHCC_04851 | 4.1e-186 | thiL_1 | S | AIR synthase related protein, C-terminal domain | ||
CNHFAHCC_04852 | 9.3e-49 | P | flavoprotein involved in K transport | |||
CNHFAHCC_04853 | 6.7e-72 | L | PFAM transposase, IS4 family protein | |||
CNHFAHCC_04854 | 1.4e-107 | S | Domain of unknown function (DUF4142) | |||
CNHFAHCC_04855 | 5.2e-130 | KT | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_04856 | 1.2e-255 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_04857 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | haloacid dehalogenase-like hydrolase | |
CNHFAHCC_04858 | 2.1e-55 | smtB | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
CNHFAHCC_04859 | 8.2e-54 | yfjF | S | PFAM Uncharacterised BCR, YnfA UPF0060 family | ||
CNHFAHCC_04860 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | ATPase, P-type (transporting), HAD superfamily, subfamily IC | |
CNHFAHCC_04861 | 3.4e-208 | cobH | 5.4.99.60, 5.4.99.61 | HK | MerR family regulatory protein | |
CNHFAHCC_04862 | 2.1e-228 | nreB | EGP | Transmembrane secretion effector | ||
CNHFAHCC_04863 | 3.2e-139 | 3.2.1.17 | G | Phage lysozyme | ||
CNHFAHCC_04864 | 0.0 | cecA_2 | P | AcrB/AcrD/AcrF family | ||
CNHFAHCC_04865 | 2.3e-100 | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | |||
CNHFAHCC_04866 | 1.5e-129 | K | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_04867 | 1.1e-256 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_04868 | 2.1e-38 | umuC | 2.7.7.7 | L | Nucleotidyltransferase DNA polymerase involved in DNA repair | |
CNHFAHCC_04869 | 2.7e-105 | T | HPP family | |||
CNHFAHCC_04870 | 2.4e-272 | pncB | 2.4.2.12 | H | Nicotinate phosphoribosyltransferase (NAPRTase) family | |
CNHFAHCC_04871 | 5e-198 | nadM | 2.7.7.1, 3.6.1.13, 3.6.1.55 | F | Cytidylyltransferase-like | |
CNHFAHCC_04872 | 9e-26 | D | Antitoxin Phd_YefM, type II toxin-antitoxin system | |||
CNHFAHCC_04873 | 7.7e-35 | S | PFAM PIN domain | |||
CNHFAHCC_04874 | 2.6e-70 | S | transposase or invertase | |||
CNHFAHCC_04875 | 1.9e-152 | map | 3.4.11.18 | J | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
CNHFAHCC_04876 | 3.2e-26 | S | CopG-like RHH_1 or ribbon-helix-helix domain, RHH_5 | |||
CNHFAHCC_04877 | 1.1e-164 | bla | 3.5.2.6 | V | Penicillin binding protein transpeptidase domain | |
CNHFAHCC_04878 | 1.2e-94 | 3.5.3.18 | J | Endoribonuclease L-PSP | ||
CNHFAHCC_04879 | 7.9e-21 | 3.5.3.18 | J | Endoribonuclease L-PSP | ||
CNHFAHCC_04880 | 3.1e-148 | azoB | GM | NmrA-like family | ||
CNHFAHCC_04881 | 2.8e-29 | |||||
CNHFAHCC_04882 | 6.9e-139 | S | CAAX protease self-immunity | |||
CNHFAHCC_04884 | 4.6e-129 | S | KR domain | |||
CNHFAHCC_04885 | 7.4e-160 | 1.11.1.10 | I | Alpha/beta hydrolase family | ||
CNHFAHCC_04886 | 4.8e-102 | O | DSBA-like thioredoxin domain | |||
CNHFAHCC_04887 | 4.5e-109 | T | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_04888 | 0.0 | 2.7.13.3 | T | Histidine kinase | ||
CNHFAHCC_04889 | 5e-14 | T | Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase | |||
CNHFAHCC_04890 | 1.1e-203 | K | DNA-templated transcription, initiation | |||
CNHFAHCC_04891 | 2e-219 | 3.4.24.3 | C | Protein of unknown function (DUF1822) | ||
CNHFAHCC_04892 | 1.4e-181 | T | Chase2 domain | |||
CNHFAHCC_04895 | 5.9e-282 | C | cobalamin binding | |||
CNHFAHCC_04896 | 1.5e-225 | ybeL | 1.17.4.1, 4.6.1.1 | J | xyloglucan:xyloglucosyl transferase activity | |
CNHFAHCC_04897 | 0.0 | S | Domain of unknown function DUF87 | |||
CNHFAHCC_04898 | 5e-98 | K | Acetyltransferase (GNAT) domain | |||
CNHFAHCC_04899 | 1.6e-293 | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | ||
CNHFAHCC_04900 | 1.2e-106 | ydjX | S | SNARE associated Golgi protein | ||
CNHFAHCC_04901 | 7.8e-196 | S | Protein of unknown function (DUF3641) | |||
CNHFAHCC_04902 | 7.5e-188 | arsM | 2.1.1.137 | Q | ubiE/COQ5 methyltransferase family | |
CNHFAHCC_04903 | 0.0 | T | diguanylate cyclase | |||
CNHFAHCC_04904 | 0.0 | ppsA | 2.7.9.2 | F | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
CNHFAHCC_04905 | 4.5e-111 | S | COGs COG4636 conserved | |||
CNHFAHCC_04906 | 7.3e-140 | V | Chloramphenicol acetyltransferase | |||
CNHFAHCC_04907 | 1.8e-118 | fraH | T | zinc-ribbon domain | ||
CNHFAHCC_04908 | 1.3e-134 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
CNHFAHCC_04909 | 6.3e-140 | minD | D | Cellulose biosynthesis protein BcsQ | ||
CNHFAHCC_04910 | 9.1e-44 | minE | D | Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell | ||
CNHFAHCC_04911 | 9.9e-19 | |||||
CNHFAHCC_04913 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
CNHFAHCC_04914 | 8.1e-274 | penP | 3.5.2.6 | V | Beta-lactamase enzyme family | |
CNHFAHCC_04915 | 1.5e-130 | trmJ | 2.1.1.200, 3.5.1.19, 6.1.1.16 | J | Catalyzes the formation of 2'O-methylated cytidine (Cm32) or 2'O-methylated uridine (Um32) at position 32 in tRNA | |
CNHFAHCC_04916 | 1.1e-170 | rbn | S | Virulence factor BrkB | ||
CNHFAHCC_04917 | 1.1e-269 | thiC | 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
CNHFAHCC_04918 | 8.7e-122 | L | DDE superfamily endonuclease | |||
CNHFAHCC_04919 | 2.7e-50 | L | transposition | |||
CNHFAHCC_04920 | 1.3e-139 | pcyA | 1.3.7.5 | Q | Catalyzes the four-electron reduction of biliverdin IX- alpha (2-electron reduction at both the A and D rings) | |
CNHFAHCC_04921 | 7.2e-135 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_04922 | 2.2e-274 | pkn5 | 3.1.3.3 | KT | stage II sporulation protein E | |
CNHFAHCC_04923 | 1.2e-92 | |||||
CNHFAHCC_04924 | 1.5e-41 | |||||
CNHFAHCC_04925 | 1.7e-111 | parA | D | VirC1 protein | ||
CNHFAHCC_04926 | 9.8e-266 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_04927 | 0.0 | S | ABC1 family | |||
CNHFAHCC_04928 | 4.8e-265 | ylbE | GM | Complex I intermediate-associated protein 30 (CIA30) | ||
CNHFAHCC_04929 | 3.8e-176 | M | Small-conductance mechanosensitive channel | |||
CNHFAHCC_04930 | 3.7e-219 | |||||
CNHFAHCC_04932 | 1.1e-200 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
CNHFAHCC_04933 | 2e-241 | cobL | 2.1.1.132, 2.1.1.196 | H | Putative methyltransferase | |
CNHFAHCC_04934 | 4.2e-228 | ama | S | Peptidase dimerisation domain | ||
CNHFAHCC_04935 | 5.8e-49 | |||||
CNHFAHCC_04936 | 1.6e-126 | K | Rho termination factor, N-terminal domain | |||
CNHFAHCC_04937 | 2.9e-265 | D | ATPase MipZ | |||
CNHFAHCC_04938 | 1e-201 | |||||
CNHFAHCC_04939 | 5.7e-220 | S | von Willebrand factor type A domain | |||
CNHFAHCC_04940 | 0.0 | yqfF | S | 7TM-HD extracellular | ||
CNHFAHCC_04941 | 2.6e-199 | |||||
CNHFAHCC_04942 | 3.7e-112 | eda | 2.7.1.45, 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
CNHFAHCC_04943 | 5.5e-286 | nrgA | P | Ammonium Transporter Family | ||
CNHFAHCC_04944 | 3.3e-194 | L | DDE superfamily endonuclease | |||
CNHFAHCC_04945 | 6e-179 | M | Glycosyl transferase family 2 | |||
CNHFAHCC_04946 | 3.8e-66 | aroH | 2.7.4.25, 5.4.99.5 | E | Catalyzes the Claisen rearrangement of chorismate to prephenate. Probably involved in the aromatic amino acid biosynthesis | |
CNHFAHCC_04947 | 5e-268 | gltS | E | Sodium/glutamate symporter | ||
CNHFAHCC_04948 | 1.5e-211 | wecB | 5.1.3.14 | G | UDP-N-acetylglucosamine 2-epimerase | |
CNHFAHCC_04949 | 7.6e-94 | ycf36 | S | Protein of unknown function (DUF1230) | ||
CNHFAHCC_04950 | 8.5e-198 | ansA | 3.5.1.1 | E | L-asparaginase II | |
CNHFAHCC_04951 | 3.3e-55 | trxA | O | Thioredoxin | ||
CNHFAHCC_04952 | 1.3e-245 | yhiN | S | HI0933-like protein | ||
CNHFAHCC_04953 | 1.4e-270 | pyk | 2.7.1.40 | F | Pyruvate kinase, barrel domain | |
CNHFAHCC_04954 | 2.1e-79 | |||||
CNHFAHCC_04955 | 1.1e-39 | 1.18.1.3 | C | 2Fe-2S iron-sulfur cluster binding domain | ||
CNHFAHCC_04956 | 2.2e-201 | 4.1.1.46 | E | amidohydrolase | ||
CNHFAHCC_04957 | 1e-292 | cobQ | 6.3.5.10 | H | Catalyzes amidations at positions B, D, E, and G on adenosylcobyrinic A,C-diamide. NH(2) groups are provided by glutamine, and one molecule of ATP is hydrogenolyzed for each amidation | |
CNHFAHCC_04958 | 1.5e-308 | mscM | M | mechanosensitive ion channel | ||
CNHFAHCC_04959 | 2.1e-236 | P | PFAM Chloride channel | |||
CNHFAHCC_04960 | 3.7e-40 | |||||
CNHFAHCC_04961 | 4.3e-236 | EGP | Major Facilitator Superfamily | |||
CNHFAHCC_04962 | 0.0 | mdlA | V | ABC transporter transmembrane region | ||
CNHFAHCC_04963 | 1.3e-196 | glk | 2.7.1.2 | F | Glucokinase | |
CNHFAHCC_04964 | 8.7e-113 | K | helix_turn_helix, cAMP Regulatory protein | |||
CNHFAHCC_04965 | 7e-77 | |||||
CNHFAHCC_04966 | 4.6e-137 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
CNHFAHCC_04967 | 1.7e-188 | S | AI-2E family transporter | |||
CNHFAHCC_04968 | 2.6e-216 | queA | 2.4.2.29, 2.4.99.17 | F | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
CNHFAHCC_04969 | 8.1e-131 | bioD | 6.3.3.3 | H | Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring | |
CNHFAHCC_04970 | 1.2e-177 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
CNHFAHCC_04971 | 1.4e-98 | S | Protein of unknown function (DUF2808) | |||
CNHFAHCC_04972 | 0.0 | 1.5.99.6 | E | FAD dependent oxidoreductase | ||
CNHFAHCC_04973 | 1.6e-144 | S | PFAM Pentapeptide repeats (8 copies) | |||
CNHFAHCC_04974 | 1.3e-165 | EG | EamA-like transporter family | |||
CNHFAHCC_04975 | 1.6e-128 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
CNHFAHCC_04976 | 4.5e-45 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
CNHFAHCC_04977 | 6e-54 | scrB | 3.2.1.26 | GH32 | G | Alpha-L-arabinofuranosidase B (ABFB) domain |
CNHFAHCC_04978 | 1.1e-120 | K | FR47-like protein | |||
CNHFAHCC_04979 | 1.6e-180 | P | NMT1/THI5 like | |||
CNHFAHCC_04980 | 0.0 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_04981 | 5.9e-27 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_04982 | 1.4e-127 | |||||
CNHFAHCC_04983 | 2.1e-199 | futA1 | P | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_04984 | 1.4e-122 | U | MotA/TolQ/ExbB proton channel family | |||
CNHFAHCC_04985 | 1.5e-74 | exbD | U | Biopolymer transport protein ExbD/TolR | ||
CNHFAHCC_04986 | 6.9e-75 | exbD | U | Biopolymer transport protein ExbD/TolR | ||
CNHFAHCC_04987 | 2e-16 | yurQ | 2.7.7.7 | L | Excinuclease ABC C subunit | |
CNHFAHCC_04988 | 1.5e-154 | L | Transposase | |||
CNHFAHCC_04989 | 2e-291 | MT | Cyclic nucleotide-monophosphate binding domain | |||
CNHFAHCC_04990 | 4.3e-112 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
CNHFAHCC_04991 | 6.1e-243 | dapL | 2.6.1.83 | E | Involved in the synthesis of meso-diaminopimelate (m-DAP or DL-DAP), required for both lysine and peptidoglycan biosynthesis. Catalyzes the direct conversion of tetrahydrodipicolinate to LL-diaminopimelate | |
CNHFAHCC_04992 | 9.2e-83 | |||||
CNHFAHCC_04993 | 1.5e-219 | 3.1.1.3 | I | Protein of unknown function (DUF2974) | ||
CNHFAHCC_04994 | 1.8e-186 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_04995 | 6.6e-41 | U | WD40-like Beta Propeller Repeat | |||
CNHFAHCC_04996 | 9.8e-138 | KLT | PFAM Ycf66 protein N-terminus | |||
CNHFAHCC_04997 | 1.2e-194 | cobW | S | Cobalamin synthesis protein cobW C-terminal domain | ||
CNHFAHCC_04998 | 9.9e-132 | hrtA | V | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_04999 | 1.5e-161 | T | cheY-homologous receiver domain | |||
CNHFAHCC_05000 | 3.4e-49 | kaiB | T | KaiB | ||
CNHFAHCC_05001 | 1.2e-238 | H | Mycolic acid cyclopropane synthetase | |||
CNHFAHCC_05002 | 1.9e-112 | S | Putative restriction endonuclease | |||
CNHFAHCC_05003 | 1.3e-116 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
CNHFAHCC_05004 | 5.9e-183 | ccmA | 3.6.3.7 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |
CNHFAHCC_05005 | 4.3e-124 | RB9536 | U | Ion channel | ||
CNHFAHCC_05006 | 1.6e-291 | U | Sulfate permease family | |||
CNHFAHCC_05007 | 3.2e-121 | 2.1.1.104 | S | O-methyltransferase | ||
CNHFAHCC_05008 | 2e-188 | dnaJ3 | O | DnaJ C terminal domain | ||
CNHFAHCC_05009 | 3.6e-148 | MA20_42350 | 2.4.1.83, 2.7.8.12 | GT2 | M | Glycosyltransferase like family 2 |
CNHFAHCC_05010 | 1.4e-264 | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | ||
CNHFAHCC_05011 | 1.8e-200 | hppD | 1.13.11.27, 1.13.11.46 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
CNHFAHCC_05012 | 2.3e-175 | 2.1.1.295, 2.1.1.95 | Q | Putative S-adenosyl-L-methionine-dependent methyltransferase | ||
CNHFAHCC_05013 | 0.0 | crtO | Q | FAD dependent oxidoreductase | ||
CNHFAHCC_05014 | 1.3e-309 | O | MreB/Mbl protein | |||
CNHFAHCC_05015 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
CNHFAHCC_05016 | 1.8e-118 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
CNHFAHCC_05017 | 4.8e-204 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
CNHFAHCC_05018 | 1.9e-267 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
CNHFAHCC_05019 | 3.6e-257 | rimO | 2.8.4.4 | J | Catalyzes the methylthiolation of an aspartic acid residue of ribosomal protein S12 | |
CNHFAHCC_05020 | 1.4e-141 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_05021 | 4.7e-90 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CNHFAHCC_05022 | 0.0 | NU | Type II secretion system (T2SS), protein E, N-terminal domain | |||
CNHFAHCC_05023 | 4.4e-70 | queD | 4.1.2.50, 4.2.3.12 | F | 6-pyruvoyl tetrahydropterin synthase | |
CNHFAHCC_05024 | 1.6e-108 | gmhA | 2.7.7.71, 5.3.1.28 | G | Catalyzes the isomerization of sedoheptulose 7-phosphate in D-glycero-D-manno-heptose 7-phosphate | |
CNHFAHCC_05025 | 1.1e-90 | gmhB | 3.1.3.82, 3.1.3.83 | G | Polynucleotide kinase 3 phosphatase | |
CNHFAHCC_05026 | 2.4e-239 | M | transferase activity, transferring glycosyl groups | |||
CNHFAHCC_05027 | 2.7e-227 | arsA | 3.6.3.16 | P | Anion-transporting ATPase | |
CNHFAHCC_05028 | 3.9e-245 | sufS | 2.8.1.7, 4.4.1.16 | E | Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family | |
CNHFAHCC_05029 | 1.7e-254 | sufD | O | Uncharacterized protein family (UPF0051) | ||
CNHFAHCC_05030 | 7.2e-141 | sufC | O | ABC transporter | ||
CNHFAHCC_05031 | 2.4e-278 | sufB | O | Uncharacterized protein family (UPF0051) | ||
CNHFAHCC_05032 | 2.3e-133 | sufR | K | Bacterial regulatory protein, arsR family | ||
CNHFAHCC_05033 | 6.3e-163 | 2.7.13.3 | T | Histidine Phosphotransfer domain | ||
CNHFAHCC_05034 | 1.4e-152 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
CNHFAHCC_05035 | 5.7e-51 | mutS2 | L | negative regulation of DNA recombination | ||
CNHFAHCC_05036 | 2.9e-84 | coaD | 2.7.7.3 | F | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
CNHFAHCC_05037 | 0.0 | cph2 | T | Phytochrome region | ||
CNHFAHCC_05038 | 7.7e-85 | iscR | 2.8.1.7 | K | Transcriptional regulator | |
CNHFAHCC_05039 | 9.5e-65 | abrB | K | AbrB-like transcriptional regulator | ||
CNHFAHCC_05040 | 1.3e-144 | 1.3.5.1, 1.3.5.4 | C | 2Fe-2S iron-sulfur cluster binding domain | ||
CNHFAHCC_05041 | 1.7e-107 | |||||
CNHFAHCC_05042 | 1.5e-30 | |||||
CNHFAHCC_05043 | 0.0 | nuoL | 1.6.5.3 | CP | NADH-dehyrogenase subunit F, TMs, (complex I) C-terminus | |
CNHFAHCC_05044 | 1.8e-45 | ycf34 | S | Hypothetical chloroplast protein Ycf34 | ||
CNHFAHCC_05045 | 1.9e-236 | cca | 2.7.7.19, 2.7.7.72 | J | tRNA nucleotidyltransferase domain 2 putative | |
CNHFAHCC_05046 | 1.6e-232 | yhjK | T | Cyclic nucleotide-monophosphate binding domain | ||
CNHFAHCC_05047 | 8.4e-162 | MA20_05910 | O | META domain | ||
CNHFAHCC_05048 | 9.6e-259 | S | Protein conserved in bacteria | |||
CNHFAHCC_05049 | 4.4e-291 | nylA | 3.5.1.4 | J | Amidase | |
CNHFAHCC_05050 | 1.8e-228 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
CNHFAHCC_05051 | 1.7e-119 | rapQ | 2.1.1.163, 2.1.1.201 | J | Tellurite resistance protein TehB | |
CNHFAHCC_05052 | 2.9e-198 | purM | 6.3.3.1, 6.3.4.13 | F | AIR synthase related protein, C-terminal domain | |
CNHFAHCC_05053 | 0.0 | fusA2 | J | Elongation factor G, domain IV | ||
CNHFAHCC_05054 | 8.4e-41 | |||||
CNHFAHCC_05055 | 1.7e-206 | rfbB | 4.2.1.46 | M | Male sterility protein | |
CNHFAHCC_05056 | 1.1e-164 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
CNHFAHCC_05057 | 0.0 | dnaB | 3.6.4.12, 5.99.1.3 | L | Participates in initiation and elongation during chromosome replication | |
CNHFAHCC_05058 | 1.7e-42 | |||||
CNHFAHCC_05059 | 1.5e-73 | sll0832 | L | Likely ribonuclease with RNase H fold. | ||
CNHFAHCC_05060 | 1.1e-209 | oppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
CNHFAHCC_05061 | 4.3e-287 | bicA | U | Sulfate permease family | ||
CNHFAHCC_05062 | 0.0 | 2.7.7.65, 2.7.7.7 | KT | HAMP domain | ||
CNHFAHCC_05063 | 3.2e-228 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
CNHFAHCC_05064 | 4.5e-32 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
CNHFAHCC_05065 | 0.0 | dap2 | E | Prolyl oligopeptidase family | ||
CNHFAHCC_05066 | 5.7e-185 | 1.1.1.271 | GM | RmlD substrate binding domain | ||
CNHFAHCC_05067 | 2.4e-236 | S | Domain of unknown function (DUF4105) | |||
CNHFAHCC_05068 | 3.6e-171 | P | PBP superfamily domain | |||
CNHFAHCC_05069 | 7e-21 | |||||
CNHFAHCC_05070 | 2.5e-56 | mliC | S | Membrane-bound lysozyme-inhibitor of c-type lysozyme | ||
CNHFAHCC_05071 | 2.6e-241 | ynbB | 4.4.1.1 | P | Methionine gamma-lyase | |
CNHFAHCC_05072 | 5.9e-193 | desC | 1.14.19.1 | I | Fatty acid desaturase | |
CNHFAHCC_05073 | 8.6e-49 | |||||
CNHFAHCC_05074 | 0.0 | acsA | 6.2.1.1 | F | Catalyzes the conversion of acetate into acetyl-CoA (AcCoA), an essential intermediate at the junction of anabolic and catabolic pathways. AcsA undergoes a two-step reaction. In the first half reaction, AcsA combines acetate with ATP to form acetyl-adenylate (AcAMP) intermediate. In the second half reaction, it can then transfer the acetyl group from AcAMP to the sulfhydryl group of CoA, forming the product AcCoA | |
CNHFAHCC_05075 | 1.5e-95 | S | Protein of unknown function (DUF2854) | |||
CNHFAHCC_05076 | 3e-251 | cyp | Q | Cytochrome P450 | ||
CNHFAHCC_05077 | 6.4e-09 | L | Phage integrase family | |||
CNHFAHCC_05078 | 2e-35 | cyaA | 4.6.1.1 | S | triphosphatase activity | |
CNHFAHCC_05079 | 7.2e-77 | |||||
CNHFAHCC_05080 | 1.7e-38 | S | Interferon-induced transmembrane protein | |||
CNHFAHCC_05081 | 7.7e-79 | S | Protein of unknown function (DUF2752) | |||
CNHFAHCC_05082 | 1.7e-69 | |||||
CNHFAHCC_05083 | 1e-187 | holA | 2.7.7.7 | L | DNA polymerase III, delta subunit | |
CNHFAHCC_05084 | 7.3e-129 | 3.6.1.27 | I | Acid phosphatase homologues | ||
CNHFAHCC_05085 | 1.3e-54 | yciH | J | Translation initiation factor SUI1 | ||
CNHFAHCC_05086 | 3.5e-120 | S | Tetratricopeptide repeat | |||
CNHFAHCC_05087 | 9.4e-299 | nusA | S | Domain of unknown function(DUF2779) | ||
CNHFAHCC_05088 | 1.1e-137 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | ||
CNHFAHCC_05089 | 0.0 | norV | 1.6.3.4 | C | Mediates electron transfer from NADH to oxygen, reducing it to water. This modular protein has 3 redox cofactors, in other organisms the same activity requires 2 or 3 proteins | |
CNHFAHCC_05090 | 1e-184 | CO | VKc | |||
CNHFAHCC_05091 | 6e-45 | |||||
CNHFAHCC_05092 | 1.9e-169 | acoC | 2.3.1.12 | I | Serine aminopeptidase, S33 | |
CNHFAHCC_05093 | 8.7e-65 | ftrC | 1.8.7.2 | C | Catalytic subunit of the ferredoxin-thioredoxin reductase (FTR), which catalyzes the two-electron reduction of thioredoxins by the electrons provided by reduced ferredoxin | |
CNHFAHCC_05094 | 1.3e-148 | map | 3.4.11.18 | E | Metallopeptidase family M24 | |
CNHFAHCC_05096 | 0.0 | nhaP | P | Sodium/hydrogen exchanger family | ||
CNHFAHCC_05097 | 1.7e-246 | natB | E | Receptor family ligand binding region | ||
CNHFAHCC_05098 | 1.1e-125 | S | Tic22-like family | |||
CNHFAHCC_05099 | 2.8e-57 | ycf65 | J | Probably a ribosomal protein or a ribosome-associated protein | ||
CNHFAHCC_05100 | 3.7e-113 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
CNHFAHCC_05101 | 2.4e-36 | S | Protein of unknown function (DUF2811) | |||
CNHFAHCC_05102 | 2.7e-32 | ndhO | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | ||
CNHFAHCC_05103 | 5.4e-178 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
CNHFAHCC_05104 | 2e-79 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
CNHFAHCC_05105 | 1.8e-83 | 1.1.1.169, 3.1.3.25, 3.6.1.55 | F | NUDIX domain | ||
CNHFAHCC_05106 | 1.1e-85 | S | Protein of unknown function, DUF393 | |||
CNHFAHCC_05107 | 1.6e-145 | map | 3.4.11.18 | J | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
CNHFAHCC_05108 | 3.9e-256 | bioF | 2.3.1.29, 2.3.1.47 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
CNHFAHCC_05109 | 7.1e-80 | L | PD-(D/E)XK endonuclease | |||
CNHFAHCC_05110 | 0.0 | |||||
CNHFAHCC_05111 | 6.1e-299 | |||||
CNHFAHCC_05112 | 8e-148 | E | O-methyltransferase activity | |||
CNHFAHCC_05113 | 8.3e-217 | ksgA | 2.1.1.182, 2.1.1.184 | J | Methyltransferase FkbM domain | |
CNHFAHCC_05114 | 0.0 | ccmI | HO | Methyltransferase FkbM domain | ||
CNHFAHCC_05115 | 1.3e-306 | psbB | U | One of the components of the core complex of photosystem II (PSII). It binds chlorophyll and helps catalyze the primary light-induced photochemical processes of PSII. PSII is a light- driven water plastoquinone oxidoreductase, using light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation | ||
CNHFAHCC_05116 | 3.5e-301 | bchE | 1.21.98.3 | F | IX monomethyl ester oxidative cyclase | |
CNHFAHCC_05117 | 9.1e-289 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
CNHFAHCC_05118 | 1.4e-44 | S | Protein of unknown function (DUF4090) | |||
CNHFAHCC_05119 | 4.7e-81 | moaE | 2.7.7.80, 2.8.1.11, 2.8.1.12 | H | MoaE protein | |
CNHFAHCC_05120 | 7.6e-36 | moaD | 2.7.7.77, 2.8.1.12, 4.6.1.17 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
CNHFAHCC_05121 | 1.7e-201 | moaC | 2.7.7.77, 4.6.1.17 | F | MoaC family | |
CNHFAHCC_05122 | 1.8e-184 | moaA | 4.1.99.22 | F | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
CNHFAHCC_05123 | 1.3e-229 | moeA | 2.10.1.1 | F | MoeA C-terminal region (domain IV) | |
CNHFAHCC_05124 | 4.6e-79 | cynS | 4.2.1.104 | P | Catalyzes the reaction of cyanate with bicarbonate to produce ammonia and carbon dioxide | |
CNHFAHCC_05125 | 6.2e-298 | nirA | 1.7.7.1 | P | Nitrite and sulphite reductase 4Fe-4S domain | |
CNHFAHCC_05126 | 0.0 | 3.2.1.4, 3.2.1.78 | GH26,GH5,GH9 | G | CBD_II | |
CNHFAHCC_05127 | 2.4e-256 | norM | U | MatE | ||
CNHFAHCC_05128 | 8.2e-102 | betI9 | K | Bacterial regulatory proteins, tetR family | ||
CNHFAHCC_05129 | 8.8e-57 | S | Tetratricopeptide repeat | |||
CNHFAHCC_05130 | 3.5e-252 | pmbA | S | Putative modulator of DNA gyrase | ||
CNHFAHCC_05131 | 1e-30 | metH | 2.1.1.13 | E | methionine synthase | |
CNHFAHCC_05132 | 5.2e-104 | S | Putative restriction endonuclease | |||
CNHFAHCC_05133 | 0.0 | T | Nacht domain | |||
CNHFAHCC_05134 | 1.2e-28 | |||||
CNHFAHCC_05135 | 4.1e-08 | S | nucleic acid-binding protein contains PIN domain | |||
CNHFAHCC_05136 | 8.2e-40 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_05137 | 2.5e-19 | N | HicA toxin of bacterial toxin-antitoxin, | |||
CNHFAHCC_05138 | 0.0 | metH | 2.1.1.13 | E | B12 binding domain | |
CNHFAHCC_05139 | 1e-234 | K | Acetyltransferase, gnat family | |||
CNHFAHCC_05140 | 1.9e-35 | S | Protein of unknown function (DUF2839) | |||
CNHFAHCC_05141 | 1.3e-245 | F | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_05142 | 3.6e-196 | S | PAS domain | |||
CNHFAHCC_05143 | 1.1e-36 | ftrV | S | Ferredoxin thioredoxin reductase variable alpha chain | ||
CNHFAHCC_05144 | 2.5e-141 | 5.2.1.8 | G | PPIC-type PPIASE domain | ||
CNHFAHCC_05145 | 0.0 | 2.3.1.82 | S | Zeta toxin | ||
CNHFAHCC_05146 | 1.5e-280 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
CNHFAHCC_05147 | 2e-76 | 3.1.2.28 | S | Thioesterase-like superfamily | ||
CNHFAHCC_05148 | 1.5e-163 | M | Barrel-sandwich domain of CusB or HlyD membrane-fusion | |||
CNHFAHCC_05149 | 1.8e-20 | N | HicA toxin of bacterial toxin-antitoxin, | |||
CNHFAHCC_05150 | 7.2e-32 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_05151 | 3.9e-12 | |||||
CNHFAHCC_05152 | 0.0 | S | SbmA/BacA-like family | |||
CNHFAHCC_05153 | 3e-26 | S | NAD(P)H dehydrogenase subunit S | |||
CNHFAHCC_05154 | 2.8e-92 | S | TPR repeat | |||
CNHFAHCC_05155 | 1.9e-46 | ylmG | S | YGGT family | ||
CNHFAHCC_05156 | 4e-173 | hdrB | C | Cysteine-rich domain | ||
CNHFAHCC_05157 | 1.9e-204 | sigC | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_05158 | 1.5e-177 | egtC | 3.5.1.118 | S | Glutamine amidotransferases class-II | |
CNHFAHCC_05159 | 1.5e-244 | S | Rho termination factor, N-terminal domain | |||
CNHFAHCC_05160 | 0.0 | comEA | 2.4.1.21 | GT5 | IL | Phospholipase D. Active site motifs. |
CNHFAHCC_05161 | 3.1e-68 | S | Protein conserved in bacteria | |||
CNHFAHCC_05162 | 3.5e-81 | U | WD40-like Beta Propeller Repeat | |||
CNHFAHCC_05163 | 3e-117 | rpiA | 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
CNHFAHCC_05164 | 1.1e-75 | rbp3 | S | RNA recognition motif | ||
CNHFAHCC_05165 | 4.3e-61 | pspE | P | Rhodanese Homology Domain | ||
CNHFAHCC_05166 | 0.0 | lytB | D | Stage II sporulation protein | ||
CNHFAHCC_05167 | 7.6e-203 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
CNHFAHCC_05168 | 1.3e-86 | yraN | L | Uncharacterised protein family UPF0102 | ||
CNHFAHCC_05169 | 2.7e-238 | cinA | 3.5.1.42 | S | Competence-damaged protein | |
CNHFAHCC_05170 | 7.2e-121 | folE | 3.5.4.16 | F | GTP cyclohydrolase I | |
CNHFAHCC_05172 | 9.6e-92 | pyrR | 2.4.2.9 | F | Phosphoribosyl transferase domain | |
CNHFAHCC_05173 | 1.4e-69 | |||||
CNHFAHCC_05174 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
CNHFAHCC_05175 | 2.4e-308 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
CNHFAHCC_05176 | 4.5e-32 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
CNHFAHCC_05177 | 3.9e-21 | hicA | N | PFAM YcfA-like protein | ||
CNHFAHCC_05178 | 9e-91 | S | Protein of unknown function (DUF3177) | |||
CNHFAHCC_05179 | 5.3e-245 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
CNHFAHCC_05180 | 1.5e-135 | urtE | E | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_05181 | 2.9e-171 | rlpA | M | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
CNHFAHCC_05182 | 6.3e-48 | |||||
CNHFAHCC_05183 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
CNHFAHCC_05184 | 6.2e-137 | cobA | 1.3.1.76, 2.1.1.107, 4.2.1.75, 4.99.1.4 | H | Tetrapyrrole (Corrin/Porphyrin) Methylases | |
CNHFAHCC_05185 | 1.7e-139 | yndB | 3.1.1.45 | Q | Dienelactone hydrolase | |
CNHFAHCC_05186 | 8.9e-127 | |||||
CNHFAHCC_05187 | 1.6e-139 | lpxA | 2.3.1.129 | I | Involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell | |
CNHFAHCC_05188 | 1.2e-213 | rfbW | M | Glycosyl transferases group 1 | ||
CNHFAHCC_05189 | 7.8e-48 | |||||
CNHFAHCC_05191 | 3.5e-18 | |||||
CNHFAHCC_05192 | 2.9e-162 | |||||
CNHFAHCC_05193 | 4.5e-95 | P | PFAM Nickel transport complex, NikM subunit, transmembrane | |||
CNHFAHCC_05194 | 1.5e-112 | cbiM | P | Cobalt uptake substrate-specific transmembrane region | ||
CNHFAHCC_05195 | 2.4e-136 | cbiQ | P | Cobalt transport protein | ||
CNHFAHCC_05196 | 4.6e-143 | P | ATPases associated with a variety of cellular activities | |||
CNHFAHCC_05197 | 1.3e-178 | S | Calcineurin-like phosphoesterase superfamily domain | |||
CNHFAHCC_05198 | 0.0 | gyrA | 5.99.1.3 | Z | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
CNHFAHCC_05199 | 2.2e-70 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_05200 | 0.0 | napA | P | Sodium/hydrogen exchanger family | ||
CNHFAHCC_05201 | 1.3e-116 | |||||
CNHFAHCC_05202 | 4.4e-120 | 3.1.3.73, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
CNHFAHCC_05203 | 5e-122 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_05204 | 1.8e-124 | S | Protein of unknown function (DUF1361) | |||
CNHFAHCC_05205 | 4e-256 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
CNHFAHCC_05206 | 8.2e-108 | S | NYN domain | |||
CNHFAHCC_05207 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
CNHFAHCC_05208 | 7.6e-157 | nit | S | Carbon-nitrogen hydrolase | ||
CNHFAHCC_05209 | 6.4e-10 | |||||
CNHFAHCC_05210 | 1.8e-278 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
CNHFAHCC_05211 | 3.4e-109 | S | von Willebrand factor (vWF) type A domain | |||
CNHFAHCC_05212 | 0.0 | prpC | 3.1.3.16 | T | Serine/threonine phosphatases, family 2C, catalytic domain | |
CNHFAHCC_05213 | 0.0 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
CNHFAHCC_05214 | 3.1e-203 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
CNHFAHCC_05215 | 5.4e-264 | E | Periplasmic binding protein | |||
CNHFAHCC_05216 | 5.2e-273 | S | PFAM Peptidase family M50 | |||
CNHFAHCC_05217 | 3.5e-269 | U | BT1 family | |||
CNHFAHCC_05218 | 9.4e-55 | ycf49 | S | Protein of unknown function (DUF2499) | ||
CNHFAHCC_05219 | 9.9e-52 | S | Protein of unknown function (DUF3593) | |||
CNHFAHCC_05220 | 4.4e-247 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_05221 | 1.8e-156 | mscS | U | Mechanosensitive ion channel | ||
CNHFAHCC_05222 | 1.7e-178 | glyQ | 6.1.1.14 | J | Glycyl-tRNA synthetase alpha subunit | |
CNHFAHCC_05223 | 1.1e-141 | NU | Tfp pilus assembly protein FimV | |||
CNHFAHCC_05226 | 4e-147 | cobS | 2.7.8.26 | H | Joins adenosylcobinamide-GDP and alpha-ribazole to generate adenosylcobalamin (Ado-cobalamin). Also synthesizes adenosylcobalamin 5'-phosphate from adenosylcobinamide-GDP and alpha-ribazole 5'-phosphate | |
CNHFAHCC_05227 | 2.7e-79 | |||||
CNHFAHCC_05228 | 1.6e-182 | ygfZ | 2.1.2.10 | S | Aminomethyltransferase folate-binding domain | |
CNHFAHCC_05229 | 2e-74 | L | Protein of unknown function (DUF3782) | |||
CNHFAHCC_05230 | 0.0 | thiG | 1.4.3.19, 2.8.1.10 | H | Thiazole biosynthesis protein ThiG | |
CNHFAHCC_05231 | 2.4e-198 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
CNHFAHCC_05232 | 8.7e-74 | S | Domain of unknown function (DUF4253) | |||
CNHFAHCC_05233 | 9.3e-107 | S | Uncharacterized protein family UPF0016 | |||
CNHFAHCC_05234 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
CNHFAHCC_05235 | 8e-133 | ymaE | S | Metallo-beta-lactamase superfamily | ||
CNHFAHCC_05237 | 1.4e-118 | pspA | KT | PspA/IM30 family | ||
CNHFAHCC_05238 | 8.6e-47 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
CNHFAHCC_05239 | 6.4e-19 | rom | S | Rop protein | ||
CNHFAHCC_05240 | 2.9e-63 | mbeC | S | Psort location Cytoplasmic, score | ||
CNHFAHCC_05241 | 1.2e-214 | tetA | EGP | Sugar (and other) transporter | ||
CNHFAHCC_05242 | 1.2e-242 | tetL | EGP | Major Facilitator Superfamily | ||
CNHFAHCC_05243 | 2e-160 | penP | 3.5.2.6 | V | Beta-lactamase | |
CNHFAHCC_05244 | 3.5e-220 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
CNHFAHCC_05245 | 3.3e-200 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
CNHFAHCC_05246 | 4e-292 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
CNHFAHCC_05247 | 3.1e-192 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
CNHFAHCC_05248 | 3.2e-84 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
CNHFAHCC_05249 | 0.0 | ilvB | 2.2.1.6 | E | Acetolactate synthase | |
CNHFAHCC_05251 | 7.6e-82 | ysnE | K | acetyltransferase | ||
CNHFAHCC_05252 | 9.1e-134 | ysnF | S | protein conserved in bacteria | ||
CNHFAHCC_05254 | 1.4e-92 | ysnB | S | Phosphoesterase | ||
CNHFAHCC_05255 | 4.5e-103 | rdgB | 3.6.1.66 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
CNHFAHCC_05256 | 1.8e-133 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
CNHFAHCC_05257 | 2.9e-196 | gerM | S | COG5401 Spore germination protein | ||
CNHFAHCC_05258 | 1.2e-154 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
CNHFAHCC_05259 | 2.3e-75 | ysmB | 2.4.2.28 | K | helix_turn_helix multiple antibiotic resistance protein | |
CNHFAHCC_05260 | 3.3e-30 | gerE | K | Transcriptional regulator | ||
CNHFAHCC_05261 | 7.7e-79 | ybgC | 3.1.2.23, 3.1.2.28 | S | thioesterase | |
CNHFAHCC_05262 | 4.6e-148 | sdhB | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
CNHFAHCC_05263 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
CNHFAHCC_05264 | 2.4e-107 | sdhC | C | succinate dehydrogenase | ||
CNHFAHCC_05265 | 1.2e-79 | yslB | S | Protein of unknown function (DUF2507) | ||
CNHFAHCC_05266 | 1.3e-216 | lysC | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
CNHFAHCC_05267 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
CNHFAHCC_05268 | 2e-52 | trxA | O | Belongs to the thioredoxin family | ||
CNHFAHCC_05269 | 4e-305 | xsa | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
CNHFAHCC_05271 | 4.2e-178 | etfA | C | Electron transfer flavoprotein | ||
CNHFAHCC_05272 | 1.2e-135 | etfB | C | Electron transfer flavoprotein | ||
CNHFAHCC_05273 | 3.1e-136 | fadB | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
CNHFAHCC_05274 | 1.9e-95 | fadR | K | Transcriptional regulator | ||
CNHFAHCC_05275 | 0.0 | lcfA | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
CNHFAHCC_05276 | 7.3e-68 | yshE | S | membrane | ||
CNHFAHCC_05277 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
CNHFAHCC_05278 | 0.0 | polX | L | COG1796 DNA polymerase IV (family X) | ||
CNHFAHCC_05279 | 1.3e-85 | cvpA | S | membrane protein, required for colicin V production | ||
CNHFAHCC_05280 | 2.4e-40 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
CNHFAHCC_05281 | 2e-170 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
CNHFAHCC_05282 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
CNHFAHCC_05283 | 2.8e-196 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
CNHFAHCC_05284 | 3.1e-133 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
CNHFAHCC_05285 | 2.6e-32 | sspI | S | Belongs to the SspI family | ||
CNHFAHCC_05286 | 4.4e-208 | ysfB | KT | regulator | ||
CNHFAHCC_05287 | 7.2e-264 | glcD | 1.1.3.15 | C | Glycolate oxidase subunit | |
CNHFAHCC_05288 | 5.6e-258 | glcF | C | Glycolate oxidase | ||
CNHFAHCC_05289 | 3.6e-38 | ysfE | 4.4.1.5 | E | lactoylglutathione lyase activity | |
CNHFAHCC_05291 | 0.0 | cstA | T | Carbon starvation protein | ||
CNHFAHCC_05292 | 4.6e-301 | abfA | 3.2.1.55 | GH51 | G | alpha-L-arabinofuranosidase activity |
CNHFAHCC_05293 | 3.4e-144 | araQ | G | transport system permease | ||
CNHFAHCC_05294 | 1.4e-167 | araP | G | carbohydrate transport | ||
CNHFAHCC_05295 | 2.2e-254 | araN | G | carbohydrate transport | ||
CNHFAHCC_05296 | 5e-226 | egsA | 1.1.1.261 | I | Catalyzes the NAD(P)H-dependent reduction of dihydroxyacetonephosphate (DHAP or glycerone phosphate) to glycerol 1-phosphate (G1P). The G1P thus generated is probably used for the synthesis of phosphoglycerolipids in Gram-positive bacterial species | |
CNHFAHCC_05297 | 1e-148 | araL | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
CNHFAHCC_05298 | 8.4e-133 | araD | 4.1.2.17, 4.2.1.109, 5.1.3.4 | G | COG0235 Ribulose-5-phosphate 4-epimerase and related epimerases and aldolases | |
CNHFAHCC_05299 | 0.0 | araB | 2.7.1.16 | C | Belongs to the ribulokinase family | |
CNHFAHCC_05300 | 1.9e-294 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
CNHFAHCC_05301 | 2.1e-190 | abnA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
CNHFAHCC_05302 | 4.5e-205 | ysdC | G | COG1363 Cellulase M and related proteins | ||
CNHFAHCC_05303 | 9.2e-68 | ysdB | S | Sigma-w pathway protein YsdB | ||
CNHFAHCC_05304 | 7.5e-45 | ysdA | S | Membrane | ||
CNHFAHCC_05305 | 3.6e-58 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
CNHFAHCC_05306 | 9e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
CNHFAHCC_05307 | 3.3e-86 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
CNHFAHCC_05309 | 2.4e-111 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like protein CidA. The LrgAB and CidA proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
CNHFAHCC_05310 | 2.2e-49 | lrgA | S | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgB, with the holin-like protein CidA. The LrgAB and CidA proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
CNHFAHCC_05311 | 6.3e-131 | lytT | T | COG3279 Response regulator of the LytR AlgR family | ||
CNHFAHCC_05312 | 0.0 | lytS | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_05313 | 1.5e-149 | ysaA | S | HAD-hyrolase-like | ||
CNHFAHCC_05314 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
CNHFAHCC_05315 | 3.8e-159 | ytxC | S | YtxC-like family | ||
CNHFAHCC_05316 | 4.9e-111 | ytxB | S | SNARE associated Golgi protein | ||
CNHFAHCC_05317 | 3e-173 | dnaI | L | Primosomal protein DnaI | ||
CNHFAHCC_05318 | 3.5e-266 | dnaB | L | Membrane attachment protein | ||
CNHFAHCC_05319 | 1.1e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
CNHFAHCC_05320 | 2e-67 | speH | 4.1.1.50 | E | Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine | |
CNHFAHCC_05321 | 2.8e-193 | gapB | 1.2.1.12, 1.2.1.59 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
CNHFAHCC_05322 | 9.9e-67 | ytcD | K | Transcriptional regulator | ||
CNHFAHCC_05323 | 4.9e-205 | ytbD | EGP | Major facilitator Superfamily | ||
CNHFAHCC_05324 | 8.9e-161 | ytbE | S | reductase | ||
CNHFAHCC_05325 | 7.6e-98 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
CNHFAHCC_05326 | 1.1e-107 | ytaF | P | Probably functions as a manganese efflux pump | ||
CNHFAHCC_05327 | 2e-157 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
CNHFAHCC_05328 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
CNHFAHCC_05329 | 0.0 | phoR | 2.7.13.3 | T | Signal transduction histidine kinase | |
CNHFAHCC_05330 | 8.3e-131 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_05331 | 1.1e-170 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
CNHFAHCC_05332 | 1.8e-242 | icd | 1.1.1.42 | C | isocitrate | |
CNHFAHCC_05333 | 4.7e-210 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
CNHFAHCC_05334 | 4.7e-71 | yeaL | S | membrane | ||
CNHFAHCC_05335 | 2.6e-192 | ytvI | S | sporulation integral membrane protein YtvI | ||
CNHFAHCC_05336 | 1.8e-63 | fxsA | S | COG3030 Protein affecting phage T7 exclusion by the F plasmid | ||
CNHFAHCC_05337 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
CNHFAHCC_05338 | 3.4e-180 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
CNHFAHCC_05339 | 1.6e-182 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
CNHFAHCC_05340 | 8.4e-162 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
CNHFAHCC_05341 | 1.5e-225 | ytsJ | 1.1.1.38 | C | Malate dehydrogenase | |
CNHFAHCC_05342 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
CNHFAHCC_05343 | 3.2e-56 | ytrH | S | Sporulation protein YtrH | ||
CNHFAHCC_05344 | 8.2e-69 | ytrI | ||||
CNHFAHCC_05345 | 9.2e-29 | |||||
CNHFAHCC_05346 | 7.8e-182 | nrnA | 3.1.13.3, 3.1.3.7 | S | COG0618 Exopolyphosphatase-related proteins | |
CNHFAHCC_05347 | 2.4e-47 | ytpI | S | YtpI-like protein | ||
CNHFAHCC_05348 | 8e-241 | ytoI | K | transcriptional regulator containing CBS domains | ||
CNHFAHCC_05350 | 1.2e-158 | ytnM | S | membrane transporter protein | ||
CNHFAHCC_05351 | 4.9e-240 | ytnL | 3.5.1.47 | E | hydrolase activity | |
CNHFAHCC_05352 | 6.3e-128 | ribF | 2.7.1.26, 2.7.7.2 | H | Riboflavin kinase | |
CNHFAHCC_05353 | 1e-256 | moxC | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_05354 | 2.9e-47 | ytnI | O | COG0695 Glutaredoxin and related proteins | ||
CNHFAHCC_05355 | 1.2e-185 | ytmO | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_05356 | 1e-142 | tcyN | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
CNHFAHCC_05357 | 7.6e-121 | tcyM | U | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_05358 | 3.7e-123 | tcyL | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_05359 | 1.5e-149 | tcyK | M | Bacterial periplasmic substrate-binding proteins | ||
CNHFAHCC_05360 | 9.5e-152 | tcyK | ET | Bacterial periplasmic substrate-binding proteins | ||
CNHFAHCC_05361 | 1.5e-100 | ytmI | K | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_05362 | 2.9e-173 | ytlI | K | LysR substrate binding domain | ||
CNHFAHCC_05363 | 1.7e-130 | ytkL | S | Belongs to the UPF0173 family | ||
CNHFAHCC_05364 | 1.1e-141 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_05366 | 3.1e-267 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
CNHFAHCC_05367 | 2.2e-102 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
CNHFAHCC_05368 | 8.5e-70 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
CNHFAHCC_05369 | 5.7e-86 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
CNHFAHCC_05370 | 4.1e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
CNHFAHCC_05371 | 7e-165 | ytxK | 2.1.1.72 | L | DNA methylase | |
CNHFAHCC_05372 | 2.4e-89 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
CNHFAHCC_05373 | 8.7e-70 | ytfJ | S | Sporulation protein YtfJ | ||
CNHFAHCC_05374 | 5.6e-116 | ytfI | S | Protein of unknown function (DUF2953) | ||
CNHFAHCC_05375 | 1.3e-87 | yteJ | S | RDD family | ||
CNHFAHCC_05376 | 2.4e-181 | sppA | OU | signal peptide peptidase SppA | ||
CNHFAHCC_05377 | 2.2e-148 | nadK | 2.7.1.23 | G | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
CNHFAHCC_05378 | 0.0 | ytcJ | S | amidohydrolase | ||
CNHFAHCC_05379 | 2e-307 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
CNHFAHCC_05380 | 2e-29 | sspB | S | spore protein | ||
CNHFAHCC_05381 | 3.5e-227 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
CNHFAHCC_05382 | 2.2e-210 | iscS2 | 2.8.1.7 | E | Cysteine desulfurase | |
CNHFAHCC_05383 | 4.9e-238 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
CNHFAHCC_05384 | 4.1e-274 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
CNHFAHCC_05385 | 1.6e-154 | hisK | 3.1.3.15 | E | COG1387 Histidinol phosphatase and related hydrolases of the PHP family | |
CNHFAHCC_05386 | 3.4e-109 | yttP | K | Transcriptional regulator | ||
CNHFAHCC_05387 | 1.2e-88 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
CNHFAHCC_05388 | 0.0 | ytrP | 2.7.7.65 | T | COG2199 FOG GGDEF domain | |
CNHFAHCC_05389 | 2.5e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
CNHFAHCC_05391 | 3.6e-238 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
CNHFAHCC_05392 | 0.0 | acsA | 6.2.1.1 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
CNHFAHCC_05393 | 3.6e-122 | acuA | K | Part of the acuABC operon, which is possibly involved in the breakdown of acetoin and butanediol. Acts as an acetyltransferase inactivating acetyl-CoA synthetase AcsA via acetylation at a Lys residue | ||
CNHFAHCC_05394 | 1.6e-117 | acuB | S | Domain in cystathionine beta-synthase and other proteins. | ||
CNHFAHCC_05395 | 1.9e-225 | acuC | BQ | histone deacetylase | ||
CNHFAHCC_05396 | 1.4e-125 | motS | N | Flagellar motor protein | ||
CNHFAHCC_05397 | 7.1e-147 | motA | N | flagellar motor | ||
CNHFAHCC_05398 | 1.7e-182 | ccpA | K | catabolite control protein A | ||
CNHFAHCC_05399 | 4.9e-196 | aroF | 2.5.1.54, 5.4.99.5 | E | Catalyzes the formation of 3-deoxy-D-aribino-hept-2-ulosonate 7-phosphate from phosphoenolpyruvate and D-erythrose 4-phosphate and the formation of prephenate from chorismate | |
CNHFAHCC_05400 | 4.4e-55 | ytxJ | O | Protein of unknown function (DUF2847) | ||
CNHFAHCC_05401 | 6.6e-17 | ytxH | S | COG4980 Gas vesicle protein | ||
CNHFAHCC_05402 | 2.1e-17 | ytxG | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
CNHFAHCC_05403 | 1.6e-254 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
CNHFAHCC_05404 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
CNHFAHCC_05405 | 9.7e-109 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
CNHFAHCC_05406 | 9.8e-149 | ytpQ | S | Belongs to the UPF0354 family | ||
CNHFAHCC_05407 | 2.1e-57 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
CNHFAHCC_05408 | 5.9e-79 | ytoQ | S | Nucleoside 2-deoxyribosyltransferase YtoQ | ||
CNHFAHCC_05409 | 4.7e-207 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
CNHFAHCC_05410 | 9.8e-52 | ytzB | S | small secreted protein | ||
CNHFAHCC_05411 | 0.0 | sfcA | 1.1.1.38 | C | Malate dehydrogenase | |
CNHFAHCC_05412 | 6.4e-151 | ytnP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
CNHFAHCC_05413 | 1.4e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
CNHFAHCC_05414 | 2e-45 | ytzH | S | YtzH-like protein | ||
CNHFAHCC_05415 | 6.1e-151 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
CNHFAHCC_05416 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
CNHFAHCC_05417 | 2.9e-181 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
CNHFAHCC_05418 | 1.3e-165 | ytlQ | ||||
CNHFAHCC_05419 | 4.3e-103 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
CNHFAHCC_05420 | 8.6e-173 | ytkP | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
CNHFAHCC_05421 | 7.1e-272 | pepV | 3.5.1.18 | E | Dipeptidase | |
CNHFAHCC_05422 | 7.2e-226 | pbuO | S | permease | ||
CNHFAHCC_05423 | 3.9e-207 | ythQ | U | Bacterial ABC transporter protein EcsB | ||
CNHFAHCC_05424 | 4.3e-132 | ythP | V | ABC transporter | ||
CNHFAHCC_05425 | 1.9e-29 | ytzE | K | COG1349 Transcriptional regulators of sugar metabolism | ||
CNHFAHCC_05426 | 2.6e-132 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
CNHFAHCC_05427 | 1.3e-293 | ytgP | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
CNHFAHCC_05428 | 4.5e-241 | ytfP | S | HI0933-like protein | ||
CNHFAHCC_05429 | 3.4e-283 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
CNHFAHCC_05430 | 3.1e-26 | yteV | S | Sporulation protein Cse60 | ||
CNHFAHCC_05431 | 4.8e-117 | yteU | S | Integral membrane protein | ||
CNHFAHCC_05432 | 2.6e-249 | yteT | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
CNHFAHCC_05433 | 4.6e-73 | yteS | G | transport | ||
CNHFAHCC_05434 | 8.9e-225 | yteR | 3.2.1.172 | GH105 | G | unsaturated glucuronyl hydrolase involved in regulation of bacterial surface properties, and related proteins |
CNHFAHCC_05435 | 2e-172 | lplB | G | COG4209 ABC-type polysaccharide transport system, permease component | ||
CNHFAHCC_05436 | 0.0 | ytdP | K | Transcriptional regulator | ||
CNHFAHCC_05437 | 1.2e-290 | ytcQ | G | COG1653 ABC-type sugar transport system, periplasmic component | ||
CNHFAHCC_05438 | 1.5e-144 | ytcP | G | COG0395 ABC-type sugar transport system, permease component | ||
CNHFAHCC_05439 | 9.6e-138 | udh | 1.1.1.203, 1.1.1.388 | GM | NAD dependent epimerase/dehydratase family | |
CNHFAHCC_05440 | 1.5e-225 | bioI | 1.14.14.46 | C | Cytochrome P450 | |
CNHFAHCC_05441 | 2.2e-190 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
CNHFAHCC_05442 | 6.4e-125 | bioD | 6.3.3.3 | H | Catalyzes a mechanistically unusual reaction, the ATP- dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA) to form an ureido ring | |
CNHFAHCC_05443 | 1.4e-220 | bioF | 2.3.1.29, 2.3.1.47, 6.2.1.14 | H | Catalyzes the decarboxylative condensation of pimeloyl- acyl-carrier protein and L-alanine to produce 8-amino-7- oxononanoate (AON), acyl-carrier protein , and carbon dioxide | |
CNHFAHCC_05444 | 2.4e-261 | bioA | 2.6.1.105, 2.6.1.62 | H | Catalyzes the transfer of the alpha-amino group from S- adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). It is the only animotransferase known to utilize SAM as an amino donor | |
CNHFAHCC_05445 | 1.6e-142 | bioW | 2.3.1.47, 6.2.1.14 | H | Catalyzes the transformation of pimelate into pimeloyl- CoA with concomitant hydrolysis of ATP to AMP | |
CNHFAHCC_05446 | 1.3e-173 | ytaP | S | Acetyl xylan esterase (AXE1) | ||
CNHFAHCC_05447 | 2.3e-190 | msmR | K | Transcriptional regulator | ||
CNHFAHCC_05448 | 2.3e-248 | msmE | G | Bacterial extracellular solute-binding protein | ||
CNHFAHCC_05449 | 1.5e-169 | amyD | P | ABC transporter | ||
CNHFAHCC_05450 | 1.5e-144 | amyC | P | ABC transporter (permease) | ||
CNHFAHCC_05451 | 4e-253 | melA | 3.2.1.122, 3.2.1.22, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase |
CNHFAHCC_05452 | 2.1e-51 | ytwF | P | Sulfurtransferase | ||
CNHFAHCC_05453 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
CNHFAHCC_05454 | 7.7e-55 | ytvB | S | Protein of unknown function (DUF4257) | ||
CNHFAHCC_05455 | 6e-143 | pfyP | T | Motif C-terminal to PAS motifs (likely to contribute to PAS structural domain) | ||
CNHFAHCC_05456 | 2.1e-211 | yttB | EGP | Major facilitator Superfamily | ||
CNHFAHCC_05457 | 1.8e-43 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
CNHFAHCC_05458 | 0.0 | bceB | V | ABC transporter (permease) | ||
CNHFAHCC_05459 | 1.1e-138 | bceA | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_05460 | 5.6e-186 | T | PhoQ Sensor | |||
CNHFAHCC_05461 | 5.5e-130 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_05462 | 8.5e-235 | ytrF | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
CNHFAHCC_05463 | 3.1e-127 | ytrE | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_05464 | 5.9e-148 | |||||
CNHFAHCC_05465 | 6.1e-169 | P | ABC-2 family transporter protein | |||
CNHFAHCC_05466 | 1.1e-161 | ytrB | P | abc transporter atp-binding protein | ||
CNHFAHCC_05467 | 5.1e-66 | ytrA | K | GntR family transcriptional regulator | ||
CNHFAHCC_05469 | 6.7e-41 | ytzC | S | Protein of unknown function (DUF2524) | ||
CNHFAHCC_05470 | 2.1e-190 | yhcC | S | Fe-S oxidoreductase | ||
CNHFAHCC_05471 | 4.9e-48 | ytqB | J | Putative rRNA methylase | ||
CNHFAHCC_05472 | 2e-160 | penP | 3.5.2.6 | V | Beta-lactamase | |
CNHFAHCC_05473 | 4.2e-126 | catB | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
CNHFAHCC_05474 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
CNHFAHCC_05475 | 8e-133 | ymaE | S | Metallo-beta-lactamase superfamily | ||
CNHFAHCC_05477 | 1.4e-118 | pspA | KT | PspA/IM30 family | ||
CNHFAHCC_05478 | 8.6e-47 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
CNHFAHCC_05480 | 1.2e-168 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_05481 | 2.9e-190 | pstS | P | PBP superfamily domain | ||
CNHFAHCC_05482 | 1.1e-198 | pstS | P | PBP superfamily domain | ||
CNHFAHCC_05483 | 1e-160 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
CNHFAHCC_05484 | 6.4e-146 | pstA | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_05485 | 1.1e-152 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
CNHFAHCC_05486 | 1.4e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
CNHFAHCC_05487 | 4.1e-81 | resA | O | Thioredoxin | ||
CNHFAHCC_05488 | 2.2e-143 | O | Cytochrome C biogenesis protein transmembrane region | |||
CNHFAHCC_05489 | 4.8e-94 | K | ECF sigma factor | |||
CNHFAHCC_05490 | 1.7e-140 | S | Anti-sigma-K factor rskA | |||
CNHFAHCC_05491 | 7.9e-228 | nhaS3 | P | Sodium/hydrogen exchanger family | ||
CNHFAHCC_05492 | 1.6e-39 | ntrP | S | Virulence-associated protein | ||
CNHFAHCC_05493 | 8.5e-69 | vapC | S | nucleic acid-binding protein contains PIN domain | ||
CNHFAHCC_05494 | 3.2e-104 | |||||
CNHFAHCC_05495 | 9.1e-189 | pheS | 6.1.1.20 | J | tRNA synthetases class II core domain (F) | |
CNHFAHCC_05496 | 5.4e-53 | |||||
CNHFAHCC_05497 | 8.7e-144 | acpT | 2.7.8.7 | H | 4'-phosphopantetheinyl transferase superfamily | |
CNHFAHCC_05498 | 3e-240 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
CNHFAHCC_05499 | 9.1e-197 | 1.1.1.412 | GM | NAD(P)H-binding | ||
CNHFAHCC_05500 | 4.3e-70 | wbpW | 2.7.7.13, 5.3.1.8 | G | Mannose-6-phosphate isomerase | |
CNHFAHCC_05501 | 1.8e-294 | menE | 4.2.1.113, 6.2.1.26 | IQ | AMP-binding enzyme C-terminal domain | |
CNHFAHCC_05502 | 6.4e-86 | S | Gamma-glutamyl cyclotransferase, AIG2-like | |||
CNHFAHCC_05503 | 1.1e-64 | |||||
CNHFAHCC_05504 | 1.6e-288 | murJ | S | Involved in peptidoglycan biosynthesis. Transports lipid-linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane | ||
CNHFAHCC_05505 | 1.8e-84 | KT | PAS fold | |||
CNHFAHCC_05506 | 0.0 | T | C-terminal domain of two-partite extracellular sensor domain | |||
CNHFAHCC_05507 | 1.2e-70 | 2.7.11.1 | S | CAAD domains of cyanobacterial aminoacyl-tRNA synthetase | ||
CNHFAHCC_05508 | 1.4e-144 | Q | Mycolic acid cyclopropane synthetase | |||
CNHFAHCC_05509 | 3.8e-287 | ycf46 | 3.6.4.6 | O | ATPase family associated with various cellular activities (AAA) | |
CNHFAHCC_05510 | 8.8e-141 | L | PD-(D/E)XK nuclease superfamily | |||
CNHFAHCC_05511 | 6.7e-116 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
CNHFAHCC_05512 | 3.7e-12 | psbX | U | Involved in the binding and or turnover of quinones at the Q(B) site of Photosystem II | ||
CNHFAHCC_05513 | 9e-58 | |||||
CNHFAHCC_05514 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
CNHFAHCC_05515 | 3.6e-76 | rcp1 | T | cheY-homologous receiver domain | ||
CNHFAHCC_05516 | 0.0 | aphA | 2.7.13.3 | T | PAS fold | |
CNHFAHCC_05517 | 1.3e-240 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
CNHFAHCC_05519 | 1.3e-183 | perM | S | AI-2E family transporter | ||
CNHFAHCC_05520 | 2.6e-109 | rps4 | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
CNHFAHCC_05521 | 5.3e-07 | S | Putative abortive phage resistance protein AbiGi, antitoxin | |||
CNHFAHCC_05522 | 5.4e-147 | natA | E | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_05523 | 6.7e-192 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
CNHFAHCC_05524 | 1.7e-87 | tadA | 3.5.4.3, 3.5.4.33 | FJ | MafB19-like deaminase | |
CNHFAHCC_05525 | 1.2e-123 | ethD | S | Antibiotic biosynthesis monooxygenase | ||
CNHFAHCC_05526 | 9.9e-263 | accC | 6.3.4.14, 6.4.1.2 | I | Biotin carboxylase C-terminal domain | |
CNHFAHCC_05527 | 1.9e-192 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
CNHFAHCC_05528 | 1.8e-245 | S | Peptidase M16 inactive domain | |||
CNHFAHCC_05529 | 1.8e-214 | ribD | 1.1.1.193, 3.5.4.26 | F | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
CNHFAHCC_05530 | 3.6e-122 | 2.1.1.265 | J | Protein of unknown function (DUF938) | ||
CNHFAHCC_05531 | 5.2e-228 | rlmL | 2.1.1.173, 2.1.1.264 | J | THUMP | |
CNHFAHCC_05532 | 0.0 | pilB | NU | Type II secretion system (T2SS), protein E, N-terminal domain | ||
CNHFAHCC_05533 | 1e-131 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
CNHFAHCC_05534 | 0.0 | dnaK | O | MreB/Mbl protein | ||
CNHFAHCC_05535 | 3.1e-184 | S | AI-2E family transporter | |||
CNHFAHCC_05536 | 2.8e-117 | |||||
CNHFAHCC_05537 | 9.8e-216 | S | Patatin-like phospholipase | |||
CNHFAHCC_05538 | 1.6e-51 | |||||
CNHFAHCC_05540 | 5.8e-52 | phaI | S | Poly(hydroxyalcanoate) granule associated protein (phasin) | ||
CNHFAHCC_05541 | 1.4e-74 | |||||
CNHFAHCC_05542 | 3e-210 | U | AI-2E family transporter | |||
CNHFAHCC_05543 | 4.1e-43 | S | Protein of unknown function (DUF3539) | |||
CNHFAHCC_05544 | 8.8e-153 | ET | Bacterial periplasmic substrate-binding proteins | |||
CNHFAHCC_05545 | 1.5e-183 | chlG | 2.5.1.133, 2.5.1.62 | H | UbiA prenyltransferase family | |
CNHFAHCC_05546 | 4.6e-103 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Peptidase C26 | |
CNHFAHCC_05547 | 6.5e-77 | dgkA | 2.7.1.107, 2.7.1.66 | I | Prokaryotic diacylglycerol kinase | |
CNHFAHCC_05548 | 4.3e-100 | ybeY | 2.6.99.2, 3.5.4.5 | J | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
CNHFAHCC_05549 | 1.2e-25 | S | Protein of unknown function (DUF3285) | |||
CNHFAHCC_05550 | 1.3e-85 | ilvN | 2.2.1.6 | E | ACT domain | |
CNHFAHCC_05551 | 1.4e-170 | MU | outer membrane autotransporter barrel domain protein | |||
CNHFAHCC_05552 | 8.3e-99 | gst | 2.5.1.18 | O | Glutathione S-transferase, C-terminal domain | |
CNHFAHCC_05553 | 0.0 | cpeY | CT | NACHT domain | ||
CNHFAHCC_05554 | 3.6e-148 | MA20_32445 | O | proteasome-type protease | ||
CNHFAHCC_05555 | 4.8e-140 | cah | 4.2.1.1 | P | Carbonic anhydrase | |
CNHFAHCC_05556 | 3.7e-162 | purU | 2.7.7.72, 3.5.1.10 | F | Catalyzes the hydrolysis of 10-formyltetrahydrofolate (formyl-FH4) to formate and tetrahydrofolate (FH4) | |
CNHFAHCC_05557 | 7e-197 | M | Glycosyl transferases group 1 | |||
CNHFAHCC_05558 | 1.6e-99 | 3.4.21.102 | K | Helix-turn-helix XRE-family like proteins | ||
CNHFAHCC_05559 | 7.6e-188 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
CNHFAHCC_05560 | 8.2e-34 | thiS | H | ThiS family | ||
CNHFAHCC_05561 | 2.9e-237 | LYS1 | 1.5.1.7 | E | Saccharopine dehydrogenase NADP binding domain | |
CNHFAHCC_05562 | 7e-155 | rsbQ | I | Serine aminopeptidase, S33 | ||
CNHFAHCC_05563 | 2.6e-91 | sixA | T | Phosphoglycerate mutase family | ||
CNHFAHCC_05564 | 5.9e-227 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
CNHFAHCC_05565 | 1.7e-218 | aspC | 2.6.1.1 | E | Cys/Met metabolism PLP-dependent enzyme | |
CNHFAHCC_05566 | 2.2e-14 | L | DDE superfamily endonuclease | |||
CNHFAHCC_05567 | 3.8e-287 | S | WD40 repeats | |||
CNHFAHCC_05569 | 1.6e-49 | S | Protein of unknown function (DUF3082) | |||
CNHFAHCC_05570 | 8.3e-287 | glcD | 1.1.2.4, 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
CNHFAHCC_05572 | 2e-13 | |||||
CNHFAHCC_05573 | 2.1e-143 | |||||
CNHFAHCC_05574 | 1.9e-86 | S | PIN domain | |||
CNHFAHCC_05575 | 3e-143 | ccmO | CQ | BMC | ||
CNHFAHCC_05576 | 3.6e-71 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
CNHFAHCC_05577 | 2.6e-100 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
CNHFAHCC_05578 | 7.1e-228 | 5.2.1.8 | O | Cyclophilin type peptidyl-prolyl cis-trans isomerase/CLD | ||
CNHFAHCC_05579 | 1.9e-191 | menC | 4.2.1.113, 5.1.1.20 | H | Enolase C-terminal domain-like | |
CNHFAHCC_05580 | 1.2e-91 | fcbC | S | Thioesterase superfamily | ||
CNHFAHCC_05581 | 5.3e-226 | yheB | S | Protein of unknown function (DUF445) | ||
CNHFAHCC_05582 | 3.5e-106 | S | Protein of unknown function (DUF3038) | |||
CNHFAHCC_05583 | 3.2e-97 | MU | Domain of unknown function (DUF4335) | |||
CNHFAHCC_05584 | 1.3e-120 | S | Protein of unknown function (DUF541) | |||
CNHFAHCC_05585 | 1.5e-75 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_05586 | 2.5e-183 | pilH | P | ATPases associated with a variety of cellular activities | ||
CNHFAHCC_05587 | 2.5e-276 | groL2 | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
CNHFAHCC_05588 | 3.3e-169 | O | SMART Prolyl 4-hydroxylase, alpha subunit | |||
CNHFAHCC_05589 | 2e-52 | trxM1 | 1.8.1.8, 5.3.4.1 | O | Thioredoxin-like domain | |
CNHFAHCC_05590 | 7e-121 | dedA | 3.6.1.27 | S | SNARE associated Golgi protein | |
CNHFAHCC_05591 | 3.5e-249 | lpxK | 2.7.1.130 | S | TIGRFAM conserved | |
CNHFAHCC_05592 | 2e-85 | alkA | 2.1.1.63, 3.2.2.21 | L | PFAM HhH-GPD superfamily base excision DNA repair protein | |
CNHFAHCC_05593 | 6e-157 | L | Transposase | |||
CNHFAHCC_05595 | 7.3e-158 | glxR | 1.1.1.31, 1.1.1.60 | I | NAD-binding of NADP-dependent 3-hydroxyisobutyrate dehydrogenase | |
CNHFAHCC_05596 | 2.9e-134 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
CNHFAHCC_05597 | 4.6e-117 | lonD | 3.4.21.53 | S | Found in ATP-dependent protease La (LON) | |
CNHFAHCC_05598 | 0.0 | ftsH1 | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
CNHFAHCC_05599 | 3.7e-110 | S | Putative restriction endonuclease | |||
CNHFAHCC_05600 | 1.1e-264 | NU | Pilus assembly protein PilX | |||
CNHFAHCC_05601 | 2.5e-62 | petE | 1.7.2.1 | C | Participates in electron transfer between P700 and the cytochrome b6-f complex in photosystem I | |
CNHFAHCC_05602 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_05603 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_05604 | 2e-126 | I | PFAM Fatty acid hydroxylase superfamily | |||
CNHFAHCC_05605 | 0.0 | gidA | J | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
CNHFAHCC_05606 | 0.0 | 3.1.3.3 | T | His Kinase A (phosphoacceptor) domain | ||
CNHFAHCC_05607 | 5.3e-264 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
CNHFAHCC_05608 | 1.9e-22 | S | Protein of unknown function (DUF2281) | |||
CNHFAHCC_05609 | 2.8e-66 | S | PIN domain | |||
CNHFAHCC_05610 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
CNHFAHCC_05611 | 2.5e-217 | rfbA | 2.3.1.157, 2.7.7.13, 2.7.7.23, 2.7.7.24, 5.4.2.8 | M | MobA-like NTP transferase domain | |
CNHFAHCC_05612 | 5.3e-127 | 1.14.13.81, 1.16.3.1, 4.1.99.5 | S | Catalyzes the decarbonylation of fatty aldehydes to alkanes | ||
CNHFAHCC_05613 | 3.9e-195 | 1.2.1.80 | S | Shikimate / quinate 5-dehydrogenase | ||
CNHFAHCC_05614 | 2.5e-18 | |||||
CNHFAHCC_05615 | 2.1e-78 | |||||
CNHFAHCC_05616 | 1.1e-106 | cobU | 2.7.1.156, 2.7.7.62, 6.3.5.10 | H | Cobinamide kinase / cobinamide phosphate guanyltransferase | |
CNHFAHCC_05617 | 5.8e-175 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
CNHFAHCC_05618 | 4.4e-252 | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | ||
CNHFAHCC_05619 | 0.0 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
CNHFAHCC_05621 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
CNHFAHCC_05622 | 2.2e-151 | sppA | OU | Peptidase family S49 | ||
CNHFAHCC_05623 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
CNHFAHCC_05624 | 0.0 | S | ABC1 family | |||
CNHFAHCC_05625 | 6.1e-232 | 2.6.1.83 | E | Aminotransferase class I and II | ||
CNHFAHCC_05626 | 7.6e-103 | S | Putative restriction endonuclease | |||
CNHFAHCC_05627 | 2.9e-90 | |||||
CNHFAHCC_05628 | 0.0 | NU | Outer membrane usher protein | |||
CNHFAHCC_05630 | 4e-267 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
CNHFAHCC_05631 | 1e-243 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
CNHFAHCC_05632 | 7e-98 | yckC | S | RDD family | ||
CNHFAHCC_05633 | 1.4e-49 | C | Ferredoxins are iron-sulfur proteins that transfer electrons in a wide variety of metabolic reactions | |||
CNHFAHCC_05634 | 5.2e-215 | lpxB | 2.4.1.182 | GT19 | I | Condensation of UDP-2,3-diacylglucosamine and 2,3- diacylglucosamine-1-phosphate to form lipid A disaccharide, a precursor of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell |
CNHFAHCC_05635 | 3.6e-156 | L | Transposase | |||
CNHFAHCC_05636 | 8.4e-126 | mgtC | S | PFAM MgtC family | ||
CNHFAHCC_05637 | 2.2e-88 | S | Domain of unknown function (DUF4330) | |||
CNHFAHCC_05638 | 1e-62 | rbcS | 4.1.1.39 | C | Ribulose bisphosphate carboxylase, small chain | |
CNHFAHCC_05639 | 1.3e-67 | rbcX | S | RbcX protein | ||
CNHFAHCC_05640 | 4.8e-284 | cbbL | 4.1.1.39 | G | RuBisCO catalyzes two reactions the carboxylation of D- ribulose 1,5-bisphosphate, the primary event in carbon dioxide fixation, as well as the oxidative fragmentation of the pentose substrate in the photorespiration process. Both reactions occur simultaneously and in competition at the same active site | |
CNHFAHCC_05641 | 8.6e-240 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
CNHFAHCC_05642 | 2.1e-140 | 2.7.7.13, 2.7.7.71, 3.1.3.82, 3.1.3.83 | JM | MobA-like NTP transferase domain | ||
CNHFAHCC_05643 | 1.9e-118 | ywlC | 2.7.7.87 | J | Telomere recombination | |
CNHFAHCC_05644 | 2.8e-221 | mltA | GH102 | M | MltA specific insert domain | |
CNHFAHCC_05645 | 8.1e-246 | hemL | 5.4.3.8 | H | Aminotransferase class-III | |
CNHFAHCC_05646 | 3.8e-204 | fba | 4.1.2.13 | F | Fructose-bisphosphate aldolase class-II | |
CNHFAHCC_05647 | 1.2e-222 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
CNHFAHCC_05648 | 0.0 | clpC | O | C-terminal, D2-small domain, of ClpB protein | ||
CNHFAHCC_05649 | 1.9e-239 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
CNHFAHCC_05650 | 4.7e-90 | S | Flavin reductase like domain | |||
CNHFAHCC_05651 | 5e-139 | yjfM | S | Protein of unknown function (DUF1190) | ||
CNHFAHCC_05652 | 1.6e-265 | ygiC | E | Glutathionylspermidine synthase preATP-grasp | ||
CNHFAHCC_05653 | 2.2e-156 | |||||
CNHFAHCC_05654 | 9.1e-135 | |||||
CNHFAHCC_05655 | 6.2e-184 | rimI | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | |
CNHFAHCC_05656 | 4.5e-184 | |||||
CNHFAHCC_05657 | 3.1e-256 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
CNHFAHCC_05658 | 1.2e-183 | agpB | 2.4.2.7 | EP | Binding-protein-dependent transport system inner membrane component | |
CNHFAHCC_05659 | 1.7e-110 | S | Protein of unknown function (DUF2808) | |||
CNHFAHCC_05660 | 2.5e-186 | lysDH | 1.4.1.18, 1.5.1.10, 1.5.1.7 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
CNHFAHCC_05661 | 1.6e-81 | S | KNTase C-terminal domain | |||
CNHFAHCC_05662 | 3.2e-23 | rpsU | J | Ribosomal protein S21 | ||
CNHFAHCC_05663 | 6.1e-122 | P | AAA domain, putative AbiEii toxin, Type IV TA system | |||
CNHFAHCC_05664 | 2e-148 | S | tetratricopeptide | |||
CNHFAHCC_05665 | 7.1e-124 | 3.2.1.20 | GH31 | S | Protein of unknown function DUF86 | |
CNHFAHCC_05666 | 6e-157 | L | Transposase | |||
CNHFAHCC_05667 | 2.1e-67 | L | PFAM Transposase | |||
CNHFAHCC_05668 | 1.7e-248 | S | Putative S-adenosyl-L-methionine-dependent methyltransferase | |||
CNHFAHCC_05669 | 3.6e-156 | L | Transposase | |||
CNHFAHCC_05670 | 7.3e-115 | htpX | O | Protein of unknown function (DUF3318) | ||
CNHFAHCC_05671 | 7.7e-238 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
CNHFAHCC_05672 | 1.7e-130 | ftsZ | M | Protein of unknown function (DUF3747) | ||
CNHFAHCC_05673 | 8.8e-124 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
CNHFAHCC_05674 | 9e-131 | yxlG | S | ABC-2 family transporter protein | ||
CNHFAHCC_05675 | 9.2e-294 | E | FAD dependent oxidoreductase | |||
CNHFAHCC_05676 | 0.0 | hypF | O | Acylphosphatase | ||
CNHFAHCC_05677 | 1.9e-135 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
CNHFAHCC_05678 | 5e-20 | |||||
CNHFAHCC_05679 | 6e-70 | |||||
CNHFAHCC_05680 | 4.7e-279 | M | Glycosyl transferases group 1 | |||
CNHFAHCC_05681 | 2.2e-87 | petD | U | Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions | ||
CNHFAHCC_05682 | 4.5e-123 | petB | C | Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions | ||
CNHFAHCC_05683 | 1.1e-291 | U | Involved in the tonB-independent uptake of proteins | |||
CNHFAHCC_05684 | 1e-181 | ET | Bacterial periplasmic substrate-binding proteins | |||
CNHFAHCC_05685 | 7.7e-175 | perM | S | AI-2E family transporter | ||
CNHFAHCC_05686 | 1.6e-126 | tpiA | 2.7.2.3, 5.1.3.39, 5.3.1.1, 5.3.1.33 | F | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
CNHFAHCC_05687 | 4.1e-104 | 3.5.1.28 | S | Sporulation and spore germination | ||
CNHFAHCC_05688 | 2.2e-218 | T | May be involved in signal transduction. Participates in the KaiABC clock protein complex, which constitutes the main circadian regulator in cyanobacteria, via its interaction with KaiC. Required for robustness of the circadian rhythm of gene expression and is involved in clock outputs | |||
CNHFAHCC_05689 | 5e-284 | 1.4.3.4 | E | Flavin containing amine oxidoreductase | ||
CNHFAHCC_05690 | 3e-110 | ycf22 | Q | ABC-type transport system involved in resistance to organic solvents periplasmic component | ||
CNHFAHCC_05691 | 4.2e-161 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
CNHFAHCC_05692 | 6.2e-28 | ycf33 | S | Protein of unknown function (DUF751) | ||
CNHFAHCC_05693 | 1.3e-64 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
CNHFAHCC_05694 | 6.1e-111 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
CNHFAHCC_05695 | 8e-111 | |||||
CNHFAHCC_05696 | 2.1e-85 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
CNHFAHCC_05698 | 9.2e-286 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
CNHFAHCC_05699 | 7.9e-106 | S | Domain of unknown function (DUF4126) | |||
CNHFAHCC_05700 | 8.3e-185 | ccmA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
CNHFAHCC_05701 | 2.1e-152 | ycf38 | U | ABC-2 family transporter protein | ||
CNHFAHCC_05702 | 3e-57 | |||||
CNHFAHCC_05703 | 2.7e-83 | ftsZ | NU | Tfp pilus assembly protein FimV | ||
CNHFAHCC_05704 | 2.6e-208 | urtD | S | Branched-chain amino acid ATP-binding cassette transporter | ||
CNHFAHCC_05707 | 1.4e-161 | yceA | S | Rhodanese Homology Domain | ||
CNHFAHCC_05708 | 4.7e-134 | radC | E | RadC-like JAB domain | ||
CNHFAHCC_05709 | 6.3e-28 | rpmI | J | Ribosomal protein L35 | ||
CNHFAHCC_05710 | 2.6e-53 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
CNHFAHCC_05711 | 3.7e-116 | lpxD | 2.3.1.191 | I | Catalyzes the N-acylation of UDP-3-O-acylglucosamine using 3-hydroxyacyl-ACP as the acyl donor. Is involved in the biosynthesis of lipid A, a phosphorylated glycolipid that anchors the lipopolysaccharide to the outer membrane of the cell | |
CNHFAHCC_05712 | 4.4e-164 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
CNHFAHCC_05713 | 1.7e-249 | secD | 6.3.2.2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | |
CNHFAHCC_05714 | 8.2e-260 | gtr | U | Sugar (and other) transporter | ||
CNHFAHCC_05715 | 0.0 | M | Carbohydrate-selective porin, OprB family | |||
CNHFAHCC_05716 | 1.1e-121 | trkA | P | TrkA-C domain | ||
CNHFAHCC_05717 | 2.2e-298 | chlB | 1.3.7.7 | F | Component of the dark-operative protochlorophyllide reductase (DPOR) that uses Mg-ATP and reduced ferredoxin to reduce ring D of protochlorophyllide (Pchlide) to form chlorophyllide a (Chlide). This reaction is light-independent. The NB-protein (ChlN-ChlB) is the catalytic component of the complex | |
CNHFAHCC_05718 | 3.7e-57 | |||||
CNHFAHCC_05719 | 6.6e-56 | S | Protein of unknown function (DUF433) | |||
CNHFAHCC_05720 | 6e-114 | S | L,D-transpeptidase catalytic domain | |||
CNHFAHCC_05721 | 8e-128 | comF | 2.4.2.14 | S | TIGRFAM comF family protein | |
CNHFAHCC_05722 | 6e-216 | iscS | 2.8.1.7 | E | Beta-eliminating lyase | |
CNHFAHCC_05723 | 2.6e-241 | E | GDSL-like Lipase/Acylhydrolase | |||
CNHFAHCC_05724 | 1.1e-26 | S | Wd-40 repeat | |||
CNHFAHCC_05725 | 1.4e-74 | |||||
CNHFAHCC_05726 | 8.7e-281 | gnd | 1.1.1.343, 1.1.1.44 | F | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
CNHFAHCC_05727 | 8.5e-237 | sqdX | M | Glycosyl transferase 4-like | ||
CNHFAHCC_05728 | 2.7e-108 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
CNHFAHCC_05729 | 1.1e-141 | 1.1.1.100 | S | KR domain | ||
CNHFAHCC_05730 | 2.8e-69 | gloA | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
CNHFAHCC_05731 | 5.8e-266 | U | CHAT domain | |||
CNHFAHCC_05732 | 5.2e-121 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
CNHFAHCC_05733 | 0.0 | 3.5.1.97 | S | Penicillin amidase | ||
CNHFAHCC_05734 | 4.4e-209 | T | PFAM Adenylate and Guanylate cyclase catalytic domain | |||
CNHFAHCC_05735 | 4.5e-58 | S | Protein of unknown function (DUF1257) | |||
CNHFAHCC_05736 | 3.1e-281 | 3.6.4.6 | O | ATPase family associated with various cellular activities (AAA) | ||
CNHFAHCC_05737 | 2.4e-65 | |||||
CNHFAHCC_05738 | 5.2e-286 | gcs2 | S | Circularly permuted ATP-grasp type 2 | ||
CNHFAHCC_05739 | 4e-189 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
CNHFAHCC_05740 | 6.8e-253 | T | His Kinase A (phosphoacceptor) domain | |||
CNHFAHCC_05741 | 4e-259 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Aldehyde dehydrogenase family | |
CNHFAHCC_05742 | 0.0 | V | AcrB/AcrD/AcrF family | |||
CNHFAHCC_05743 | 0.0 | yeeJ | 3.2.1.8 | S | protein secretion | |
CNHFAHCC_05744 | 3.5e-108 | S | Protein of unknown function (DUF721) | |||
CNHFAHCC_05745 | 2.8e-12 | psbI | U | PSII is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation | ||
CNHFAHCC_05746 | 0.0 | M | Protein of unknown function (DUF3769) | |||
CNHFAHCC_05747 | 4.5e-94 | yqeG | S | Mitochondrial PGP phosphatase | ||
CNHFAHCC_05748 | 1e-136 | rsuA | 5.4.99.19, 5.4.99.20, 5.4.99.22 | J | S4 RNA-binding domain | |
CNHFAHCC_05749 | 9.9e-302 | pbuG | P | secondary active sulfate transmembrane transporter activity | ||
CNHFAHCC_05750 | 0.0 | 2.7.7.65 | T | Putative diguanylate phosphodiesterase | ||
CNHFAHCC_05751 | 7.1e-300 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
CNHFAHCC_05752 | 2.8e-257 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
CNHFAHCC_05753 | 5.1e-102 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
CNHFAHCC_05754 | 3.7e-111 | |||||
CNHFAHCC_05755 | 1.1e-104 | |||||
CNHFAHCC_05756 | 1.6e-148 | S | Beta-lactamase superfamily domain | |||
CNHFAHCC_05757 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
CNHFAHCC_05758 | 2.7e-128 | ccmC | O | Prokaryotic cytochrome b561 | ||
CNHFAHCC_05759 | 4e-33 | |||||
CNHFAHCC_05760 | 5.4e-147 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
CNHFAHCC_05761 | 2.9e-53 | L | Transposase | |||
CNHFAHCC_05762 | 8.4e-190 | L | PFAM Transposase | |||
CNHFAHCC_05763 | 7.3e-200 | S | Dynamin family | |||
CNHFAHCC_05764 | 2.8e-76 | KT | Phage shock protein A | |||
CNHFAHCC_05765 | 0.0 | S | Anaphase-promoting complex subunit 4 WD40 domain | |||
CNHFAHCC_05766 | 3.1e-289 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase HemD | |
CNHFAHCC_05767 | 1.5e-86 | |||||
CNHFAHCC_05768 | 3.8e-59 | |||||
CNHFAHCC_05769 | 0.0 | O | Protein of unknown function (DUF4101) | |||
CNHFAHCC_05770 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
CNHFAHCC_05771 | 1.7e-212 | gcvT | 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
CNHFAHCC_05772 | 1e-81 | |||||
CNHFAHCC_05773 | 5.3e-195 | vgb | V | Inactivates the type B streptogramin antibiotics by linearizing the lactone ring at the ester linkage, generating a free phenylglycine carboxylate and converting the threonyl moiety into 2-amino-butenoic acid | ||
CNHFAHCC_05774 | 9.4e-158 | ET | Bacterial periplasmic substrate-binding proteins | |||
CNHFAHCC_05775 | 0.0 | IV02_08645 | S | FAD-dependent | ||
CNHFAHCC_05776 | 6e-31 | |||||
CNHFAHCC_05777 | 2.1e-33 | |||||
CNHFAHCC_05778 | 1.5e-78 | S | Metal-sensitive transcriptional repressor | |||
CNHFAHCC_05779 | 5.2e-256 | L | Recombinase | |||
CNHFAHCC_05780 | 6.6e-81 | S | Domain in cystathionine beta-synthase and other proteins. | |||
CNHFAHCC_05781 | 1.3e-88 | S | Tetratricopeptide repeat | |||
CNHFAHCC_05782 | 3.4e-112 | CQ | BMC | |||
CNHFAHCC_05783 | 0.0 | 1.7.2.1 | Q | Multicopper oxidase | ||
CNHFAHCC_05784 | 5.4e-178 | mviM | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
CNHFAHCC_05786 | 4.1e-92 | NU | Tfp pilus assembly protein FimV | |||
CNHFAHCC_05787 | 3.7e-237 | S | NurA | |||
CNHFAHCC_05788 | 0.0 | G | Glycosyl hydrolase family 57 | |||
CNHFAHCC_05789 | 0.0 | coaE | 2.7.1.24, 2.7.7.24 | GH | This protein is postulated to act both as terminal energy acceptor (by its phycobilin-like domains) and as a linker polypeptide (by its repeats and arms) that stabilizes the phycobilisome core architecture. Has intrinsic bilin lyase activity (By similarity) | |
CNHFAHCC_05790 | 2.4e-155 | S | Haloacid dehalogenase-like hydrolase | |||
CNHFAHCC_05792 | 2.6e-55 | |||||
CNHFAHCC_05793 | 5.2e-53 | 3.5.1.28 | T | Bacterial SH3 domain | ||
CNHFAHCC_05794 | 2.4e-292 | ndhD | 1.6.5.3 | C | NDH-1 shuttles electrons from NAD(P)H, via FMN and iron- sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient | |
CNHFAHCC_05795 | 2.5e-23 | psaC | C | essential for photochemical activity. FB is the terminal electron acceptor of PSI, donating electrons to ferredoxin. The C-terminus interacts with PsaA B D and helps assemble the protein into the PSI complex. Required for binding of PsaD and PsaE to PSI. PSI is a plastocyanin cytochrome c6- ferredoxin oxidoreductase, converting photonic excitation into a charge separation, which transfers an electron from the donor P700 chlorophyll pair to the spectroscopically characterized acceptors A0, A1, FX, FA and FB in turn | ||
CNHFAHCC_05796 | 6.4e-44 | K | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_05797 | 6.2e-102 | S | COGs COG4636 conserved | |||
CNHFAHCC_05798 | 6.8e-91 | yacP | S | YacP-like NYN domain | ||
CNHFAHCC_05799 | 2.5e-112 | S | Uncharacterized protein conserved in bacteria (DUF2062) | |||
CNHFAHCC_05800 | 3.8e-173 | glcK | 2.7.1.2 | GK | ROK family | |
CNHFAHCC_05801 | 4.3e-76 | ptpA | 3.1.3.48 | T | Low molecular weight phosphatase family | |
CNHFAHCC_05802 | 0.0 | fbpB | P | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_05803 | 6.3e-81 | |||||
CNHFAHCC_05804 | 2.6e-126 | ribE | 2.5.1.9 | H | Lumazine binding domain | |
CNHFAHCC_05805 | 2e-30 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_05806 | 7.3e-91 | S | MEKHLA domain | |||
CNHFAHCC_05807 | 4.8e-157 | oppC | U | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_05808 | 0.0 | ams1 | 3.2.1.24 | GH38 | G | Alpha mannosidase, middle domain |
CNHFAHCC_05809 | 0.0 | pilL | 2.7.13.3 | T | Signal transducing histidine kinase, homodimeric domain | |
CNHFAHCC_05810 | 1e-173 | era | J | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
CNHFAHCC_05811 | 4.7e-177 | sigB | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
CNHFAHCC_05812 | 0.0 | C | Elongator protein 3, MiaB family, Radical SAM | |||
CNHFAHCC_05813 | 3.3e-58 | S | Domain of unknown function (DUF1830) | |||
CNHFAHCC_05814 | 1.5e-288 | glgA | 2.4.1.21 | GT5 | G | Starch synthase catalytic domain |
CNHFAHCC_05816 | 7.8e-48 | |||||
CNHFAHCC_05817 | 8.2e-110 | lipB | 2.3.1.181, 2.8.1.8 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domains of lipoate-dependent enzymes. Lipoyl-ACP can also act as a substrate although octanoyl-ACP is likely to be the physiological substrate | |
CNHFAHCC_05818 | 4.9e-102 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
CNHFAHCC_05819 | 0.0 | nlpD | 3.4.24.75 | M | Lysin motif | |
CNHFAHCC_05820 | 6.7e-86 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
CNHFAHCC_05821 | 2.5e-222 | gshA | S | Glutamate-cysteine ligase family 2(GCS2) | ||
CNHFAHCC_05822 | 3.1e-136 | yebC | K | Transcriptional regulator | ||
CNHFAHCC_05823 | 4.6e-82 | T | Forkhead associated domain | |||
CNHFAHCC_05824 | 0.0 | zntA | 3.6.3.4 | P | Heavy-metal-associated domain | |
CNHFAHCC_05825 | 4.4e-112 | S | Protein of unknown function (DUF3318) | |||
CNHFAHCC_05826 | 3.9e-179 | pdhC | 1.8.1.4, 2.3.1.12 | C | 2-oxoacid dehydrogenases acyltransferase (catalytic domain) | |
CNHFAHCC_05827 | 5.5e-152 | O | Zinc-dependent metalloprotease | |||
CNHFAHCC_05828 | 4.8e-32 | secG | U | Preprotein translocase SecG subunit | ||
CNHFAHCC_05829 | 0.0 | gpmI | 5.4.2.12 | F | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
CNHFAHCC_05830 | 0.0 | S | Alpha/beta hydrolase of unknown function (DUF1400) | |||
CNHFAHCC_05831 | 1.5e-172 | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 | |
CNHFAHCC_05832 | 1.6e-24 | S | Proto-chlorophyllide reductase 57 kD subunit | |||
CNHFAHCC_05833 | 7.7e-288 | kaiC | T | DnaB-like helicase C terminal domain | ||
CNHFAHCC_05834 | 9e-86 | T | TspO/MBR family | |||
CNHFAHCC_05835 | 2.2e-38 | S | PFAM Uncharacterised BCR, COG1649 | |||
CNHFAHCC_05836 | 2.1e-162 | |||||
CNHFAHCC_05837 | 0.0 | O | Peptidase family M48 | |||
CNHFAHCC_05838 | 5.2e-127 | plsC | 2.3.1.51, 2.7.4.25 | I | Phosphate acyltransferases | |
CNHFAHCC_05839 | 2.8e-196 | mtnA | 5.3.1.23 | E | Catalyzes the interconversion of methylthioribose-1- phosphate (MTR-1-P) into methylthioribulose-1-phosphate (MTRu-1- P) | |
CNHFAHCC_05840 | 4.9e-127 | P | PFAM Rieske 2Fe-2S domain | |||
CNHFAHCC_05841 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_05842 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_05843 | 2.5e-70 | hcaE | 1.14.13.82 | P | PFAM Rieske 2Fe-2S domain | |
CNHFAHCC_05845 | 8.3e-81 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
CNHFAHCC_05846 | 1.4e-91 | S | Protein of unknown function (DUF3750) | |||
CNHFAHCC_05847 | 1e-164 | xthA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
CNHFAHCC_05848 | 1.6e-255 | EGP | Transmembrane secretion effector | |||
CNHFAHCC_05849 | 2.7e-196 | pdhA | 1.2.4.1 | C | The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2) | |
CNHFAHCC_05850 | 0.0 | |||||
CNHFAHCC_05851 | 8.5e-104 | rfbC | 5.1.3.13 | G | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
CNHFAHCC_05852 | 3.6e-156 | L | Transposase | |||
CNHFAHCC_05853 | 5.1e-147 | L | Transposase and inactivated derivatives | |||
CNHFAHCC_05854 | 2.5e-62 | |||||
CNHFAHCC_05855 | 1.5e-17 | |||||
CNHFAHCC_05856 | 1.4e-121 | MA20_22480 | I | Ndr family | ||
CNHFAHCC_05857 | 3e-162 | NU | pilus assembly protein PilW | |||
CNHFAHCC_05858 | 8.2e-102 | NU | general secretion pathway protein | |||
CNHFAHCC_05859 | 2.3e-93 | NU | general secretion pathway protein | |||
CNHFAHCC_05860 | 1.2e-74 | ppdC | NU | Prokaryotic N-terminal methylation motif | ||
CNHFAHCC_05861 | 6.1e-235 | S | Protein of unknown function DUF58 | |||
CNHFAHCC_05862 | 1.5e-86 | smf | LU | Alternative locus ID | ||
CNHFAHCC_05863 | 0.0 | eriC | PT | Voltage gated chloride channel | ||
CNHFAHCC_05864 | 3.3e-31 | |||||
CNHFAHCC_05865 | 1.1e-165 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
CNHFAHCC_05866 | 1.2e-191 | cobD | 6.3.1.10 | H | CobD/Cbib protein | |
CNHFAHCC_05867 | 4.6e-235 | 3.4.16.4 | V | Beta-lactamase | ||
CNHFAHCC_05868 | 6.6e-234 | frhB | 1.12.98.1, 1.3.7.13 | C | Coenzyme F420 hydrogenase/dehydrogenase, beta subunit N-term | |
CNHFAHCC_05869 | 2.9e-53 | L | Transposase | |||
CNHFAHCC_05870 | 2.7e-17 | |||||
CNHFAHCC_05871 | 4.7e-35 | S | Protein of unknown function (DUF3134) | |||
CNHFAHCC_05872 | 6.1e-168 | mtnP | 2.4.2.28 | F | Catalyzes the reversible phosphorylation of S-methyl-5'- thioadenosine (MTA) to adenine and 5-methylthioribose-1-phosphate. Involved in the breakdown of MTA, a major by-product of polyamine biosynthesis. Responsible for the first step in the methionine salvage pathway after MTA has been generated from S- adenosylmethionine. Has broad substrate specificity with 6- aminopurine nucleosides as preferred substrates | |
CNHFAHCC_05873 | 3.6e-265 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
CNHFAHCC_05874 | 1.7e-108 | clpP3 | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
CNHFAHCC_05875 | 3.5e-123 | clpP | 3.4.21.92 | OU | Clp protease | |
CNHFAHCC_05876 | 7.4e-127 | pilC | U | Type II secretion system (T2SS), protein F | ||
CNHFAHCC_05877 | 5e-87 | pilC | U | Type II secretion system (T2SS), protein F | ||
CNHFAHCC_05878 | 4.7e-202 | pilT | NU | Type II/IV secretion system protein | ||
CNHFAHCC_05879 | 7.3e-176 | M | Barrel-sandwich domain of CusB or HlyD membrane-fusion | |||
CNHFAHCC_05880 | 0.0 | V | AcrB/AcrD/AcrF family | |||
CNHFAHCC_05881 | 2.4e-94 | KLT | serine threonine protein kinase | |||
CNHFAHCC_05882 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
CNHFAHCC_05883 | 1e-25 | N | mRNA binding | |||
CNHFAHCC_05884 | 8.4e-34 | S | PFAM Uncharacterised protein family UPF0150 | |||
CNHFAHCC_05885 | 4.7e-140 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
CNHFAHCC_05886 | 1.2e-89 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
CNHFAHCC_05887 | 2.1e-197 | natC | E | Branched-chain amino acid transport system / permease component | ||
CNHFAHCC_05888 | 0.0 | cruA | 5.5.1.19 | C | COGs COG0644 Dehydrogenase (flavoprotein) | |
CNHFAHCC_05889 | 0.0 | S | Caspase domain | |||
CNHFAHCC_05890 | 0.0 | S | protein complex oligomerization | |||
CNHFAHCC_05891 | 0.0 | KLT | Serine/Threonine protein kinases, catalytic domain | |||
CNHFAHCC_05892 | 1.2e-153 | S | Tetratricopeptide repeat | |||
CNHFAHCC_05893 | 1.9e-52 | 1.18.1.3 | C | 2Fe-2S iron-sulfur cluster binding domain | ||
CNHFAHCC_05894 | 1.4e-83 | S | Phycobilisome protein | |||
CNHFAHCC_05895 | 7.1e-98 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
CNHFAHCC_05896 | 1.6e-128 | IV02_16895 | S | V4R | ||
CNHFAHCC_05897 | 1e-87 | S | Phycobilisome protein | |||
CNHFAHCC_05898 | 2.5e-76 | |||||
CNHFAHCC_05899 | 2.3e-144 | IV02_16895 | S | V4R | ||
CNHFAHCC_05900 | 0.0 | hat | S | WD40 repeats | ||
CNHFAHCC_05901 | 5.8e-124 | S | Protein of unknown function (DUF1275) | |||
CNHFAHCC_05902 | 0.0 | G | Domain of unknown function (DUF4114) | |||
CNHFAHCC_05903 | 1.2e-154 | Q | Fibrillarin | |||
CNHFAHCC_05904 | 5e-198 | pyrC | 3.5.2.3 | F | Catalyzes the reversible cyclization of carbamoyl aspartate to dihydroorotate | |
CNHFAHCC_05905 | 1.7e-27 | S | Protein of unknown function (DUF2442) | |||
CNHFAHCC_05906 | 2.3e-81 | S | Domain of unknown function (DUF4281) | |||
CNHFAHCC_05907 | 9.4e-186 | U | EamA-like transporter family | |||
CNHFAHCC_05908 | 1.7e-119 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
CNHFAHCC_05909 | 2.3e-47 | |||||
CNHFAHCC_05910 | 1.7e-112 | S | Protein of unknown function (DUF1517) | |||
CNHFAHCC_05911 | 4.7e-52 | glnB | K | Belongs to the P(II) protein family | ||
CNHFAHCC_05912 | 4.7e-108 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
CNHFAHCC_05914 | 9.8e-227 | E | Bacterial extracellular solute-binding protein | |||
CNHFAHCC_05915 | 6.9e-175 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
CNHFAHCC_05916 | 7.4e-183 | ycf39 | GM | NmrA-like family | ||
CNHFAHCC_05917 | 1.7e-87 | S | PilZ domain | |||
CNHFAHCC_05918 | 3.2e-101 | S | Protein of unknown function (DUF3038) | |||
CNHFAHCC_05919 | 2.4e-83 | abrB | K | AbrB-like transcriptional regulator | ||
CNHFAHCC_05920 | 3.8e-156 | S | CAAX protease self-immunity | |||
CNHFAHCC_05921 | 6.8e-69 | |||||
CNHFAHCC_05922 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
CNHFAHCC_05923 | 8.6e-173 | ntcB | K | LysR substrate binding domain | ||
CNHFAHCC_05924 | 8.4e-213 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
CNHFAHCC_05925 | 2.9e-74 | 5.3.3.1 | S | Uncharacterized conserved protein (DUF2358) | ||
CNHFAHCC_05926 | 1.9e-11 | S | Protein of unknown function (DUF433) | |||
CNHFAHCC_05927 | 2.5e-67 | V | HNH nucleases | |||
CNHFAHCC_05928 | 7e-57 | |||||
CNHFAHCC_05929 | 4.7e-82 | |||||
CNHFAHCC_05930 | 0.0 | gcvP | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
CNHFAHCC_05931 | 1e-65 | ydiB | 2.7.1.221, 5.1.1.1 | J | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
CNHFAHCC_05932 | 4e-137 | cbiX | 1.3.1.76, 4.99.1.3, 4.99.1.4 | S | CbiX | |
CNHFAHCC_05933 | 4.8e-28 | |||||
CNHFAHCC_05934 | 4.1e-86 | psbV | C | Low-potential cytochrome c that plays a role in the oxygen-evolving complex of photosystem II | ||
CNHFAHCC_05935 | 2.4e-77 | S | Domain of unknown function DUF29 | |||
CNHFAHCC_05936 | 0.0 | glnN | 6.3.1.2 | S | Glutamine synthetase type III N terminal | |
CNHFAHCC_05937 | 1.3e-57 | CP_0960 | S | KH domain | ||
CNHFAHCC_05938 | 1.8e-37 | rpsP | J | Ribosomal protein S16 | ||
CNHFAHCC_05939 | 5.5e-245 | tlyC | S | Transporter associated domain | ||
CNHFAHCC_05940 | 4.1e-74 | |||||
CNHFAHCC_05941 | 3.3e-150 | |||||
CNHFAHCC_05942 | 1.4e-121 | M1-769 | L | Radical SAM domain protein | ||
CNHFAHCC_05943 | 7.7e-50 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
CNHFAHCC_05944 | 0.0 | P | TrkA-N domain | |||
CNHFAHCC_05945 | 2.6e-213 | desD | 1.14.19.3 | I | Fatty acid desaturase | |
CNHFAHCC_05946 | 1.1e-140 | |||||
CNHFAHCC_05947 | 1.4e-222 | P | Rieske [2Fe-2S] domain | |||
CNHFAHCC_05948 | 2.5e-169 | 1.14.13.81, 1.14.19.11, 1.14.19.2, 1.14.19.26, 1.16.3.1, 4.1.99.5 | S | Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) | ||
CNHFAHCC_05949 | 1.7e-240 | |||||
CNHFAHCC_05950 | 0.0 | T | CHASE | |||
CNHFAHCC_05951 | 7.4e-53 | XK27_07760 | S | YtxH-like protein | ||
CNHFAHCC_05952 | 1.7e-67 | |||||
CNHFAHCC_05953 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
CNHFAHCC_05954 | 0.0 | G | Phosphodiester glycosidase | |||
CNHFAHCC_05955 | 4.4e-144 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
CNHFAHCC_05956 | 1.8e-86 | S | Protein of unknown function (DUF2996) | |||
CNHFAHCC_05957 | 8e-267 | nhaS2 | U | Sodium/hydrogen exchanger family | ||
CNHFAHCC_05958 | 9.9e-42 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_05959 | 2.6e-280 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
CNHFAHCC_05960 | 4.2e-253 | urtA | E | Periplasmic binding protein domain | ||
CNHFAHCC_05962 | 7e-178 | holB | 2.7.7.7 | L | DNA polymerase III, delta subunit | |
CNHFAHCC_05963 | 1.1e-186 | 2.1.1.295, 2.1.1.95 | Q | Methionine biosynthesis protein MetW | ||
CNHFAHCC_05964 | 4.4e-77 | |||||
CNHFAHCC_05965 | 1.3e-53 | ureB | 3.5.1.5 | E | Urease beta subunit | |
CNHFAHCC_05966 | 2.6e-106 | S | Putative restriction endonuclease | |||
CNHFAHCC_05967 | 4.2e-242 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminus | |
CNHFAHCC_05968 | 3.9e-173 | 3.5.1.1 | E | Asparaginase | ||
CNHFAHCC_05970 | 1.2e-85 | |||||
CNHFAHCC_05971 | 6.4e-309 | C | Elongator protein 3, MiaB family, Radical SAM | |||
CNHFAHCC_05972 | 3.3e-250 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
CNHFAHCC_05973 | 1.3e-63 | |||||
CNHFAHCC_05975 | 5.7e-55 | |||||
CNHFAHCC_05976 | 1.4e-153 | psbO | S | Manganese-stabilising protein / photosystem II polypeptide | ||
CNHFAHCC_05977 | 5.7e-43 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
CNHFAHCC_05978 | 2.8e-19 | |||||
CNHFAHCC_05979 | 3.3e-24 | S | BrnA antitoxin of type II toxin-antitoxin system | |||
CNHFAHCC_05980 | 6.7e-36 | S | Ribonuclease toxin, BrnT, of type II toxin-antitoxin system | |||
CNHFAHCC_05981 | 1.5e-27 | S | PilT protein domain protein | |||
CNHFAHCC_05982 | 2.7e-11 | S | Protein of unknown function (DUF2281) | |||
CNHFAHCC_05983 | 5.3e-195 | O | SMART Prolyl 4-hydroxylase, alpha subunit | |||
CNHFAHCC_05984 | 8.4e-297 | infB | NU | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
CNHFAHCC_05985 | 1.6e-308 | recN | L | May be involved in recombinational repair of damaged DNA | ||
CNHFAHCC_05986 | 0.0 | norV | 1.6.3.4 | C | Mediates electron transfer from NADH to oxygen, reducing it to water. This modular protein has 3 redox cofactors, in other organisms the same activity requires 2 or 3 proteins (By similarity) | |
CNHFAHCC_05987 | 1.4e-79 | pgsA | 2.7.8.5 | I | CDP-alcohol phosphatidyltransferase | |
CNHFAHCC_05988 | 2.7e-111 | cpcT | E | Covalently attaches a chromophore to Cys residue(s) of phycobiliproteins | ||
CNHFAHCC_05989 | 8.3e-33 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
CNHFAHCC_05990 | 3.2e-40 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
CNHFAHCC_05991 | 4.7e-295 | 1.13.11.75 | Q | Retinal pigment epithelial membrane protein | ||
CNHFAHCC_05992 | 4.9e-137 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
CNHFAHCC_05993 | 1.1e-127 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
CNHFAHCC_05994 | 8e-67 | psb27 | M | Plays a role in the repair and or biogenesis of the calcium-manganese-oxide cluster on the lumenal face of the thylakoid membrane | ||
CNHFAHCC_05995 | 1.7e-154 | S | Tetratricopeptide repeat | |||
CNHFAHCC_05996 | 7.5e-152 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
CNHFAHCC_05997 | 1.2e-243 | petH | 1.14.13.208, 1.18.1.2, 1.19.1.1 | P | Oxidoreductase NAD-binding domain | |
CNHFAHCC_05998 | 9.5e-194 | prk | 2.7.1.19 | F | Phosphoribulokinase / Uridine kinase family | |
CNHFAHCC_05999 | 4.4e-46 | |||||
CNHFAHCC_06000 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
CNHFAHCC_06001 | 6.7e-292 | Q | Predicted methyltransferase regulatory domain | |||
CNHFAHCC_06002 | 0.0 | M | Glycosyl transferase 4-like domain | |||
CNHFAHCC_06003 | 0.0 | wbsE | M | Glycosyl transferase family 2 | ||
CNHFAHCC_06004 | 3.4e-227 | H | Methyltransferase FkbM domain | |||
CNHFAHCC_06005 | 0.0 | |||||
CNHFAHCC_06006 | 5.9e-82 | smpB | J | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | ||
CNHFAHCC_06007 | 1.4e-53 | S | Protein of unknown function (DUF760) | |||
CNHFAHCC_06009 | 1.7e-113 | ypuF | S | Domain of unknown function (DUF309) | ||
CNHFAHCC_06010 | 8.4e-190 | L | PFAM Transposase | |||
CNHFAHCC_06011 | 6.7e-34 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
CNHFAHCC_06012 | 2.1e-117 | |||||
CNHFAHCC_06013 | 2.3e-46 | |||||
CNHFAHCC_06014 | 2.6e-204 | pilT2 | NU | Type II/IV secretion system protein | ||
CNHFAHCC_06015 | 7.9e-221 | wcnD | M | Glycosyltransferase Family 4 | ||
CNHFAHCC_06016 | 1e-136 | wcaJ | M | Bacterial sugar transferase | ||
CNHFAHCC_06017 | 2e-180 | rluD | 5.4.99.23 | J | S4 RNA-binding domain | |
CNHFAHCC_06018 | 2.5e-76 | S | Uncharacterized protein conserved in bacteria (DUF2237) | |||
CNHFAHCC_06019 | 6.5e-226 | moeB | 2.7.7.73, 2.7.7.80, 2.8.1.11 | HP | ThiF family | |
CNHFAHCC_06020 | 4.1e-99 | U | LysE type translocator | |||
CNHFAHCC_06021 | 8.7e-78 | folB | 1.13.11.81, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
CNHFAHCC_06022 | 5.8e-76 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
CNHFAHCC_06023 | 0.0 | bgl | 3.2.1.21, 3.2.1.52 | GH3 | G | Glycosyl hydrolase family 3 N terminal domain |
CNHFAHCC_06024 | 3.6e-260 | C | dehydrogenase complex catalyzes the overall conversion of | |||
CNHFAHCC_06025 | 2e-64 | ndhM | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_06026 | 1e-124 | ppa | 3.6.1.1 | C | Inorganic pyrophosphatase | |
CNHFAHCC_06027 | 6.7e-223 | MA20_09515 | 2.4.1.83 | GT2 | M | GtrA-like protein |
CNHFAHCC_06028 | 1.3e-47 | clpS | S | ATP-dependent Clp protease adaptor protein ClpS | ||
CNHFAHCC_06029 | 4.5e-301 | 1.13.11.75 | Q | Retinal pigment epithelial membrane protein | ||
CNHFAHCC_06030 | 8.7e-75 | |||||
CNHFAHCC_06031 | 6e-291 | S | CAAX protease self-immunity | |||
CNHFAHCC_06032 | 4.8e-105 | maf | 1.1.1.25, 2.1.1.190 | D | Maf-like protein | |
CNHFAHCC_06033 | 1.9e-291 | cysS | 6.1.1.16, 6.3.1.13 | J | DALR_2 | |
CNHFAHCC_06034 | 6.6e-53 | T | Domain of unknown function (DUF1816) | |||
CNHFAHCC_06035 | 6e-176 | rlmB | 2.1.1.185 | J | RNA 2'-O ribose methyltransferase substrate binding | |
CNHFAHCC_06036 | 2.9e-75 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
CNHFAHCC_06037 | 6.3e-48 | rsbV | T | STAS domain | ||
CNHFAHCC_06038 | 4.3e-143 | mfppA | 2.4.1.14, 3.1.3.24, 3.1.3.79 | GT4 | S | Sucrose-6F-phosphate phosphohydrolase |
CNHFAHCC_06039 | 1.2e-199 | fbp | 3.1.3.11 | G | Fructose-1-6-bisphosphatase, N-terminal domain | |
CNHFAHCC_06040 | 2.9e-133 | ispD | 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
CNHFAHCC_06041 | 1e-98 | O | Heat shock protein DnaJ domain protein | |||
CNHFAHCC_06043 | 4.7e-40 | |||||
CNHFAHCC_06044 | 5.1e-153 | tlyA | 2.1.1.226, 2.1.1.227 | J | FtsJ-like methyltransferase | |
CNHFAHCC_06045 | 1.5e-155 | livH | E | Branched-chain amino acid transport system / permease component | ||
CNHFAHCC_06046 | 0.0 | yfmR | S | ABC transporter C-terminal domain | ||
CNHFAHCC_06047 | 4.1e-112 | S | Putative restriction endonuclease | |||
CNHFAHCC_06048 | 1.4e-118 | T | Cofactor assembly of complex C subunit B, CCB2/CCB4 | |||
CNHFAHCC_06049 | 1.8e-133 | T | Transcriptional regulatory protein, C terminal | |||
CNHFAHCC_06050 | 4.9e-69 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
CNHFAHCC_06051 | 8.4e-116 | arsH | S | NADPH-dependent FMN reductase | ||
CNHFAHCC_06052 | 2.7e-208 | arsB | U | Sodium Bile acid symporter family | ||
CNHFAHCC_06053 | 2.5e-219 | tomA | 3.1.4.46, 3.2.1.18, 3.2.1.8 | GH33 | E | GDSL-like Lipase/Acylhydrolase |
CNHFAHCC_06054 | 7.5e-166 | fda | 4.1.2.13 | F | Fructose-bisphosphate aldolase class-I | |
CNHFAHCC_06055 | 3.5e-185 | 1.1.1.2 | S | Aldo/keto reductase family | ||
CNHFAHCC_06056 | 6.3e-81 | S | Polyketide cyclase / dehydrase and lipid transport | |||
CNHFAHCC_06057 | 5.5e-283 | crtQ | 1.17.8.1, 1.3.5.5, 1.3.5.6 | S | Catalyzes the conversion of zeta-carotene to lycopene via the intermediary of neurosporene. It carries out two consecutive desaturations (introduction of double bonds) at positions C-7 and C-7' | |
CNHFAHCC_06058 | 2e-299 | pqqL | S | Peptidase M16 inactive domain | ||
CNHFAHCC_06059 | 2.9e-119 | cobH | 5.4.99.60, 5.4.99.61 | H | Precorrin-8X methylmutase | |
CNHFAHCC_06060 | 1.1e-261 | murE | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
CNHFAHCC_06061 | 8.5e-200 | tnpT | 2.1.1.80, 3.1.1.61 | M | protein involved in exopolysaccharide biosynthesis | |
CNHFAHCC_06062 | 3.7e-154 | nadC | 1.4.3.16, 2.4.2.19 | F | Belongs to the NadC ModD family | |
CNHFAHCC_06063 | 3.9e-78 | OU | NfeD-like C-terminal, partner-binding | |||
CNHFAHCC_06064 | 5.2e-07 | |||||
CNHFAHCC_06065 | 0.0 | ppc | 4.1.1.31 | C | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
CNHFAHCC_06066 | 1.8e-116 | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | |||
CNHFAHCC_06067 | 6.3e-270 | 2.7.11.1 | KLT | Protein tyrosine kinase | ||
CNHFAHCC_06068 | 0.0 | pheT | 6.1.1.20 | J | B3/4 domain | |
CNHFAHCC_06069 | 3.8e-81 | T | Sensors of blue-light using FAD | |||
CNHFAHCC_06070 | 4.4e-219 | cheV | T | cheY-homologous receiver domain | ||
CNHFAHCC_06071 | 6.4e-190 | yhjK | T | Putative diguanylate phosphodiesterase | ||
CNHFAHCC_06072 | 0.0 | nadE | 6.3.1.5, 6.3.5.1 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
CNHFAHCC_06073 | 7.7e-137 | 3.6.1.55 | F | NUDIX domain | ||
CNHFAHCC_06074 | 1.2e-171 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
CNHFAHCC_06075 | 1.7e-34 | psaE | S | Stabilizes the interaction between PsaC and the PSI core, assists the docking of the ferredoxin to PSI and interacts with ferredoxin-NADP oxidoreductase | ||
CNHFAHCC_06076 | 2e-205 | 2.7.13.3, 2.7.7.65 | T | cheY-homologous receiver domain | ||
CNHFAHCC_06077 | 2.5e-197 | fni | 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
CNHFAHCC_06078 | 1.1e-169 | sucD | 6.2.1.5 | C | CoA binding domain | |
CNHFAHCC_06079 | 5.1e-223 | cugP | 2.7.7.13, 5.4.2.8 | F | Catalyzes the formation of UDP-glucose, from UTP and glucose 1-phosphate | |
CNHFAHCC_06080 | 1.2e-57 | C | PBS lyase HEAT-like repeat | |||
CNHFAHCC_06081 | 1.3e-50 | fdx | 4.6.1.1 | C | 2Fe-2S iron-sulfur cluster binding domain | |
CNHFAHCC_06082 | 1.1e-69 | T | Forkhead associated domain | |||
CNHFAHCC_06083 | 1.1e-214 | dhsS | 1.12.1.2 | E | Aminotransferase class-V | |
CNHFAHCC_06084 | 6e-87 | L | transposition | |||
CNHFAHCC_06085 | 1.9e-68 | L | DDE superfamily endonuclease | |||
CNHFAHCC_06086 | 1.1e-189 | L | PFAM Transposase | |||
CNHFAHCC_06087 | 4.3e-68 | L | transposition | |||
CNHFAHCC_06088 | 1.6e-174 | |||||
CNHFAHCC_06089 | 0.0 | putA | 1.2.1.88, 1.5.5.2 | CE | Proline dehydrogenase | |
CNHFAHCC_06090 | 3.5e-82 | |||||
CNHFAHCC_06091 | 0.0 | D | Involved in chromosome partitioning | |||
CNHFAHCC_06092 | 9.8e-25 | 3.6.1.55 | F | GDP-mannose mannosyl hydrolase activity | ||
CNHFAHCC_06093 | 3.1e-40 | T | Domain of unknown function DUF29 | |||
CNHFAHCC_06094 | 1.1e-19 | 3.6.3.38 | GM | teichoic acid transport | ||
CNHFAHCC_06095 | 0.0 | cimA | 2.3.3.13 | E | LeuA allosteric (dimerisation) domain | |
CNHFAHCC_06096 | 7.9e-145 | ddpX | 3.4.13.22 | M | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
CNHFAHCC_06097 | 5.8e-42 | rpmA | J | Ribosomal L27 protein | ||
CNHFAHCC_06098 | 2.1e-61 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
CNHFAHCC_06099 | 2.1e-233 | lpxB | 2.4.1.182 | GT19 | M | lipid A disaccharide synthetase |
CNHFAHCC_06100 | 1.6e-85 | S | Protein of unknown function (DUF4079) | |||
CNHFAHCC_06101 | 1.3e-57 | hypA | S | hydrogenase nickel incorporation protein HypA | ||
CNHFAHCC_06102 | 4.1e-59 | S | Protein of unknown function (DUF760) | |||
CNHFAHCC_06103 | 6.9e-150 | spoU | 2.1.1.185 | J | RNA 2'-O ribose methyltransferase substrate binding | |
CNHFAHCC_06104 | 4.6e-293 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
CNHFAHCC_06105 | 0.0 | G | Hypothetical glycoside hydrolase 5 | |||
CNHFAHCC_06106 | 1.9e-294 | ggpS | 2.4.1.15, 2.4.1.213, 2.4.1.347, 3.1.3.12 | GT20 | F | Glycosyltransferase family 20 |
CNHFAHCC_06107 | 0.0 | glpD | 1.1.5.3 | F | C-terminal domain of alpha-glycerophosphate oxidase | |
CNHFAHCC_06108 | 1.1e-149 | S | ABC-2 family transporter protein | |||
CNHFAHCC_06109 | 1.4e-23 | |||||
CNHFAHCC_06110 | 1.2e-274 | S | Uncharacterized protein conserved in bacteria (DUF2330) | |||
CNHFAHCC_06111 | 6.6e-81 | NU | Tfp pilus assembly protein FimV | |||
CNHFAHCC_06112 | 4.6e-272 | sglT | E | Sodium:solute symporter family | ||
CNHFAHCC_06113 | 6e-117 | |||||
CNHFAHCC_06114 | 1.2e-34 | S | Protein of unknown function (DUF3493) | |||
CNHFAHCC_06115 | 7.9e-96 | gpo | 1.11.1.22, 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
CNHFAHCC_06116 | 6.8e-54 | S | Uncharacterized protein family UPF0016 | |||
CNHFAHCC_06117 | 3.5e-117 | |||||
CNHFAHCC_06118 | 2.1e-54 | S | Protein of unknown function (DUF433) | |||
CNHFAHCC_06119 | 1.5e-211 | gldA | 1.1.1.1, 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
CNHFAHCC_06120 | 1.8e-231 | chlP | 1.3.1.111, 1.3.1.83 | C | geranylgeranyl reductase | |
CNHFAHCC_06121 | 8.3e-13 | S | KAP family P-loop domain | |||
CNHFAHCC_06122 | 4.7e-31 | S | Protein of unknown function (DUF2281) | |||
CNHFAHCC_06123 | 2.6e-67 | S | PIN domain | |||
CNHFAHCC_06124 | 1.3e-204 | GT4 | M | Glycosyl transferases group 1 | ||
CNHFAHCC_06125 | 3e-231 | sat | 2.7.7.4 | P | PUA-like domain | |
CNHFAHCC_06126 | 0.0 | nrdA | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
CNHFAHCC_06127 | 2.6e-46 | |||||
CNHFAHCC_06128 | 0.0 | oprB | M | Carbohydrate-selective porin, OprB family | ||
CNHFAHCC_06129 | 2e-177 | ethD | S | Antibiotic biosynthesis monooxygenase | ||
CNHFAHCC_06130 | 6.4e-113 | FJ | Cytidine and deoxycytidylate deaminase zinc-binding region | |||
CNHFAHCC_06131 | 3.3e-08 | L | Transposase | |||
CNHFAHCC_06132 | 4.5e-21 | L | Integrase core domain | |||
CNHFAHCC_06133 | 5.7e-39 | L | DDE superfamily endonuclease | |||
CNHFAHCC_06134 | 8.3e-52 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
CNHFAHCC_06135 | 7.8e-106 | |||||
CNHFAHCC_06136 | 2e-241 | purD | 6.3.2.6, 6.3.4.13, 6.3.5.3 | F | Phosphoribosylglycinamide synthetase, ATP-grasp (A) domain | |
CNHFAHCC_06137 | 1e-124 | S | Uncharacterized protein conserved in bacteria (DUF2064) | |||
CNHFAHCC_06138 | 5.1e-63 | rpsL | J | Ribosomal protein S12/S23 | ||
CNHFAHCC_06139 | 1.3e-79 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
CNHFAHCC_06140 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
CNHFAHCC_06141 | 2.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
CNHFAHCC_06142 | 4.4e-52 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
CNHFAHCC_06143 | 7.3e-100 | dctQ | Q | Tripartite ATP-independent periplasmic transporters, DctQ component | ||
CNHFAHCC_06144 | 4.6e-236 | dctM | Q | Tripartite ATP-independent periplasmic transporter, DctM component | ||
CNHFAHCC_06145 | 1.5e-155 | glnH | ET | Bacterial periplasmic substrate-binding proteins | ||
CNHFAHCC_06146 | 2.9e-31 | |||||
CNHFAHCC_06147 | 4.1e-10 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_06148 | 1.6e-179 | ykfA | 3.4.17.13 | V | LD-carboxypeptidase | |
CNHFAHCC_06149 | 2.6e-58 | |||||
CNHFAHCC_06150 | 5.4e-129 | hypB | KO | CobW/HypB/UreG, nucleotide-binding domain | ||
CNHFAHCC_06151 | 1.8e-300 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
CNHFAHCC_06152 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
CNHFAHCC_06153 | 8.1e-282 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
CNHFAHCC_06154 | 2.9e-60 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_06155 | 2.4e-89 | L | DDE superfamily endonuclease | |||
CNHFAHCC_06156 | 2.4e-230 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
CNHFAHCC_06157 | 7.5e-23 | |||||
CNHFAHCC_06158 | 1.6e-146 | cspH | K | Cold shock | ||
CNHFAHCC_06159 | 2.4e-153 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
CNHFAHCC_06160 | 3.7e-136 | pdxH | 1.4.3.5 | H | Catalyzes the oxidation of either pyridoxine 5'- phosphate (PNP) or pyridoxamine 5'-phosphate (PMP) into pyridoxal 5'-phosphate (PLP) | |
CNHFAHCC_06161 | 9.2e-219 | desB | 1.14.19.25, 1.14.19.35, 1.14.19.36 | I | Fatty acid desaturase | |
CNHFAHCC_06162 | 0.0 | pspF | CKT | Sigma-54 interaction domain | ||
CNHFAHCC_06163 | 7.4e-61 | U | domain, Protein | |||
CNHFAHCC_06164 | 7.9e-33 | S | Domain of unknown function (DUF4926) | |||
CNHFAHCC_06165 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
CNHFAHCC_06166 | 1e-113 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
CNHFAHCC_06167 | 7.1e-13 | S | Pentapeptide repeats (9 copies) | |||
CNHFAHCC_06168 | 8.4e-66 | S | Domain of unknown function (DUF4359) | |||
CNHFAHCC_06169 | 6.4e-191 | S | AI-2E family transporter | |||
CNHFAHCC_06170 | 5.4e-98 | yyaK | S | CAAX protease self-immunity | ||
CNHFAHCC_06171 | 1.1e-192 | S | Protein of unknown function (DUF3326) | |||
CNHFAHCC_06172 | 3e-24 | |||||
CNHFAHCC_06173 | 1.9e-242 | V | Beta-lactamase | |||
CNHFAHCC_06174 | 1.1e-203 | pehS | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
CNHFAHCC_06175 | 6.9e-130 | K | Cyclic nucleotide-monophosphate binding domain | |||
CNHFAHCC_06176 | 2e-310 | T | Domain of unknown function (DUF1816) | |||
CNHFAHCC_06177 | 1.2e-85 | L | Transposase | |||
CNHFAHCC_06178 | 1.2e-58 | L | PFAM Transposase, Synechocystis PCC 6803 | |||
CNHFAHCC_06179 | 2.9e-104 | ndhJ | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_06180 | 3.6e-137 | ndhK | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_06181 | 1.9e-59 | nuoA | 1.6.5.3 | C | electron donor, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory and or the photosynthetic chain. The immediate electron acceptor for the enzyme in this species is believed to be plastoquinone. Couples the redox reaction to proton translocation, and thus conserves the redox energy in a proton gradient. Cyanobacterial NDH-1 also plays a role in inorganic carbon- concentration | |
CNHFAHCC_06182 | 2.4e-214 | thrC | 4.2.3.1 | E | Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine | |
CNHFAHCC_06183 | 8.2e-190 | tilS | 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
CNHFAHCC_06184 | 9.3e-138 | Q | Methyltransferase FkbM domain | |||
CNHFAHCC_06185 | 1.3e-156 | hb6 | D | Methyltransferase FkbM domain | ||
CNHFAHCC_06186 | 0.0 | gspD | NU | Bacterial type II/III secretion system short domain | ||
CNHFAHCC_06187 | 1.6e-130 | mshJ | NU | carbon utilization | ||
CNHFAHCC_06188 | 2.1e-149 | xpsL | NU | PFAM Fimbrial assembly protein (PilN) | ||
CNHFAHCC_06189 | 1e-201 | pilM | NU | Type IV pilus assembly protein PilM; | ||
CNHFAHCC_06190 | 1.8e-75 | |||||
CNHFAHCC_06191 | 3.1e-144 | opdC | M | S-layer homology domain | ||
CNHFAHCC_06192 | 6.4e-147 | rffM | 2.4.1.187 | GT26 | M | Glycosyl transferase WecB/TagA/CpsF family |
CNHFAHCC_06193 | 5.4e-284 | tolC | MU | Outer membrane efflux protein | ||
CNHFAHCC_06194 | 5.5e-289 | ggt | 2.3.2.2, 3.4.19.13 | E | Gamma-glutamyltranspeptidase | |
CNHFAHCC_06195 | 1.5e-217 | ftsW | 2.4.1.227 | GT28 | D | Cell cycle protein |
CNHFAHCC_06196 | 3.8e-99 | S | Protein of unknown function (DUF2808) | |||
CNHFAHCC_06197 | 0.0 | nolO | O | Carbamoyltransferase N-terminus | ||
CNHFAHCC_06198 | 0.0 | rpoC1 | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
CNHFAHCC_06199 | 0.0 | hlyB | V | Peptidase C39 family | ||
CNHFAHCC_06200 | 4.3e-274 | hlyD | MV | HlyD membrane-fusion protein of T1SS | ||
CNHFAHCC_06201 | 3.1e-71 | 1.10.9.1 | C | Rieske [2Fe-2S] domain | ||
CNHFAHCC_06202 | 1.5e-247 | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | ||
CNHFAHCC_06203 | 1e-206 | xanB | 2.7.7.13, 5.3.1.8 | M | Nucleotidyl transferase | |
CNHFAHCC_06204 | 7.7e-126 | crp1 | K | helix_turn_helix, cAMP Regulatory protein | ||
CNHFAHCC_06205 | 8.5e-148 | yybS | S | Predicted membrane protein (DUF2232) | ||
CNHFAHCC_06206 | 8.3e-99 | |||||
CNHFAHCC_06207 | 4.4e-12 | |||||
CNHFAHCC_06208 | 1.1e-305 | melB | U | MFS/sugar transport protein | ||
CNHFAHCC_06209 | 1.8e-239 | carF | 5.1.3.34 | I | short chain dehydrogenase | |
CNHFAHCC_06210 | 1.8e-178 | S | Stage II sporulation protein M | |||
CNHFAHCC_06211 | 4.4e-285 | 2.4.1.336 | GT2 | I | Glycosyl transferase family group 2 | |
CNHFAHCC_06212 | 4.1e-180 | S | Protein of unknown function (DUF1838) | |||
CNHFAHCC_06214 | 4.1e-189 | pyrB | 2.1.3.2 | F | Aspartate/ornithine carbamoyltransferase, Asp/Orn binding domain | |
CNHFAHCC_06215 | 1.3e-119 | KLT | GUN4-like | |||
CNHFAHCC_06216 | 6.7e-69 | |||||
CNHFAHCC_06217 | 2.4e-155 | spr7 | M | NlpC/P60 family | ||
CNHFAHCC_06219 | 1.4e-65 | 1.18.1.3 | C | 2Fe-2S iron-sulfur cluster binding domain | ||
CNHFAHCC_06220 | 2e-163 | suhB | 3.1.3.25 | G | Inositol monophosphatase family | |
CNHFAHCC_06221 | 1.4e-170 | O | DnaJ molecular chaperone homology domain | |||
CNHFAHCC_06222 | 3.4e-83 | jag | S | R3H domain | ||
CNHFAHCC_06223 | 3.2e-209 | yidC | U | 60Kd inner membrane protein | ||
CNHFAHCC_06224 | 5.8e-70 | rnpA | 3.1.26.5 | J | Bacterial PH domain | |
CNHFAHCC_06225 | 3.2e-46 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
CNHFAHCC_06226 | 4.1e-15 | rpmH | J | Ribosomal protein L34 | ||
CNHFAHCC_06227 | 1.3e-81 | S | EVE domain | |||
CNHFAHCC_06228 | 2.3e-113 | cobH | 5.4.99.60, 5.4.99.61 | H | Precorrin-8X methylmutase | |
CNHFAHCC_06229 | 1.6e-91 | comEA | L | COG1555 DNA uptake protein and related DNA-binding | ||
CNHFAHCC_06230 | 5.6e-154 | 3.1.3.16 | T | Calcineurin-like phosphoesterase | ||
CNHFAHCC_06231 | 1.8e-11 | petG | U | Component of the cytochrome b6-f complex, which mediates electron transfer between photosystem II (PSII) and photosystem I (PSI), cyclic electron flow around PSI, and state transitions. PetG is required for either the stability or assembly of the cytochrome b6-f complex | ||
CNHFAHCC_06233 | 2.3e-81 | uspA | T | Universal stress protein family | ||
CNHFAHCC_06234 | 3.1e-101 | |||||
CNHFAHCC_06235 | 5e-36 | |||||
CNHFAHCC_06236 | 2.3e-128 | ydjH | S | TPM domain | ||
CNHFAHCC_06237 | 1.2e-106 | sua5 | 2.7.7.87 | J | Telomere recombination | |
CNHFAHCC_06238 | 4.6e-210 | pufM | 1.10.3.9 | C | Photosystem II (PSII) is a light-driven water plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. The D1 D2 (PsbA PsbA) reaction center heterodimer binds P680, the primary electron donor of PSII as well as several subsequent electron acceptors | |
CNHFAHCC_06239 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
CNHFAHCC_06240 | 1.5e-169 | rps1b | J | Ribosomal protein S1-like RNA-binding domain | ||
CNHFAHCC_06241 | 3.6e-215 | cbaB | P | Rieske [2Fe-2S] domain | ||
CNHFAHCC_06242 | 5.6e-121 | P | ATPases associated with a variety of cellular activities | |||
CNHFAHCC_06243 | 0.0 | 3.1.3.3 | T | Sigma factor PP2C-like phosphatases | ||
CNHFAHCC_06244 | 1.2e-61 | KT | cheY-homologous receiver domain | |||
CNHFAHCC_06245 | 0.0 | T | HAMP domain | |||
CNHFAHCC_06246 | 2.1e-260 | lytR | K | LytR cell envelope-related transcriptional attenuator | ||
CNHFAHCC_06247 | 3.4e-40 | |||||
CNHFAHCC_06248 | 2.5e-208 | acsF2 | 1.14.13.81, 1.16.3.1, 4.1.99.5 | F | Catalyzes the formation of the isocyclic ring in chlorophyll biosynthesis. Mediates the cyclase reaction, which results in the formation of divinylprotochlorophyllide (Pchlide) characteristic of all chlorophylls from magnesium-protoporphyrin IX 13-monomethyl ester (MgPMME) | |
CNHFAHCC_06249 | 1.4e-141 | hmuO | 1.14.15.20 | F | Heme oxygenase | |
CNHFAHCC_06250 | 2.6e-274 | hemN | 1.3.98.3 | F | Belongs to the anaerobic coproporphyrinogen-III oxidase family | |
CNHFAHCC_06251 | 1.8e-145 | cysZ | E | Etoposide-induced protein 2.4 (EI24) | ||
CNHFAHCC_06252 | 2.1e-276 | pabB | 2.6.1.85 | EH | Anthranilate synthase component I, N terminal region | |
CNHFAHCC_06253 | 3.1e-140 | cbiQ | P | Cobalt transport protein | ||
CNHFAHCC_06254 | 9.6e-135 | MA20_16045 | 1.17.7.4, 3.2.2.9 | F | Phosphorylase superfamily | |
CNHFAHCC_06255 | 8.5e-212 | potA | 3.6.3.30 | E | ATPases associated with a variety of cellular activities | |
CNHFAHCC_06256 | 0.0 | ycf55 | T | Protein of unknown function (DUF3685) | ||
CNHFAHCC_06257 | 1.5e-79 | yjbQ | S | Uncharacterised protein family UPF0047 | ||
CNHFAHCC_06258 | 1.8e-239 | ce | 5.1.3.11, 5.1.3.8 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
CNHFAHCC_06259 | 1.6e-50 | S | Tetratricopeptide repeat | |||
CNHFAHCC_06260 | 1.2e-230 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
CNHFAHCC_06261 | 1.9e-190 | |||||
CNHFAHCC_06262 | 7.2e-261 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
CNHFAHCC_06263 | 0.0 | xylA5 | 3.2.1.37 | GH52 | NU | Alternative locus ID |
CNHFAHCC_06264 | 1.3e-110 | 1.1.9.1 | C | Dihaem cytochrome c | ||
CNHFAHCC_06265 | 8e-192 | yacL | S | Large family of predicted nucleotide-binding domains | ||
CNHFAHCC_06266 | 9.3e-36 | |||||
CNHFAHCC_06267 | 5.3e-245 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | |||
CNHFAHCC_06268 | 1.7e-151 | S | Peptidase family M48 | |||
CNHFAHCC_06269 | 5.6e-89 | S | Late competence development protein ComFB | |||
CNHFAHCC_06270 | 2.2e-31 | hfq | S | regulation of RNA biosynthetic process | ||
CNHFAHCC_06271 | 0.0 | 2.7.13.3 | T | Domain present in phytochromes and cGMP-specific phosphodiesterases. | ||
CNHFAHCC_06272 | 1.3e-107 | cobN | 6.6.1.1, 6.6.1.2 | H | COG1429 Cobalamin biosynthesis protein CobN and related | |
CNHFAHCC_06273 | 5.2e-136 | cyaD | 4.6.1.1 | T | Chase2 domain | |
CNHFAHCC_06274 | 0.0 | S | CHAT domain | |||
CNHFAHCC_06275 | 2.2e-131 | PT | iron ion homeostasis | |||
CNHFAHCC_06276 | 1.2e-143 | hisF | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | ||
CNHFAHCC_06277 | 3.9e-144 | 3.2.1.17 | G | Phage lysozyme | ||
CNHFAHCC_06278 | 0.0 | ribBA | 3.5.4.25, 4.1.99.12 | F | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
CNHFAHCC_06279 | 4.6e-52 | |||||
CNHFAHCC_06280 | 9.7e-180 | S | Nuclear transport factor 2 (NTF2) domain | |||
CNHFAHCC_06281 | 0.0 | T | Forkhead associated domain | |||
CNHFAHCC_06282 | 6.4e-215 | Q | Part of the tripartite ATP-independent periplasmic (TRAP) transport system | |||
CNHFAHCC_06283 | 2.6e-48 | D | protein conserved in cyanobacteria | |||
CNHFAHCC_06284 | 1.6e-51 | L | DDE superfamily endonuclease | |||
CNHFAHCC_06285 | 5.3e-77 | S | EVE domain | |||
CNHFAHCC_06286 | 0.0 | 2.7.7.7, 3.6.4.12 | LO | EXOIII | ||
CNHFAHCC_06287 | 8.7e-19 | rom | S | Rop protein | ||
CNHFAHCC_06288 | 2.9e-63 | mbeC | S | Psort location Cytoplasmic, score | ||
CNHFAHCC_06289 | 1.2e-214 | tetA | EGP | Sugar (and other) transporter | ||
CNHFAHCC_06290 | 1.2e-242 | tetL | EGP | Major Facilitator Superfamily | ||
CNHFAHCC_06291 | 2e-160 | penP | 3.5.2.6 | V | Beta-lactamase | |
CNHFAHCC_06292 | 5.5e-50 | ytqB | J | Putative rRNA methylase | ||
CNHFAHCC_06293 | 2e-216 | ytpB | 4.2.3.130 | S | Tetraprenyl-beta-curcumene synthase | |
CNHFAHCC_06294 | 3.3e-149 | ytpA | 3.1.1.5 | I | Alpha beta hydrolase | |
CNHFAHCC_06295 | 1.6e-59 | ytoA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
CNHFAHCC_06296 | 8.4e-257 | ytnA | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_06297 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
CNHFAHCC_06298 | 4.3e-225 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
CNHFAHCC_06299 | 2.2e-311 | pckA | 4.1.1.49 | C | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA | |
CNHFAHCC_06300 | 1.3e-37 | ytmB | S | Protein of unknown function (DUF2584) | ||
CNHFAHCC_06301 | 5.5e-149 | ytmA | E | COG1506 Dipeptidyl aminopeptidases acylaminoacyl-peptidases | ||
CNHFAHCC_06302 | 5e-190 | ytlA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
CNHFAHCC_06303 | 1.4e-144 | ytlC | P | ABC transporter | ||
CNHFAHCC_06304 | 1.8e-142 | ytlD | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
CNHFAHCC_06305 | 2.8e-87 | ytkD | 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
CNHFAHCC_06306 | 5.4e-63 | ytkC | S | Bacteriophage holin family | ||
CNHFAHCC_06307 | 2.1e-76 | dps | P | Belongs to the Dps family | ||
CNHFAHCC_06309 | 3.6e-73 | ytkA | S | YtkA-like | ||
CNHFAHCC_06310 | 1.6e-87 | luxS | 4.4.1.21 | T | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
CNHFAHCC_06311 | 8e-40 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
CNHFAHCC_06312 | 5.7e-103 | ytiB | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
CNHFAHCC_06313 | 3.6e-41 | rpmE2 | J | Ribosomal protein L31 | ||
CNHFAHCC_06314 | 4.7e-249 | cydA | 1.10.3.14 | C | oxidase, subunit | |
CNHFAHCC_06315 | 7.3e-189 | cydB | 1.10.3.14 | C | COG1294 Cytochrome bd-type quinol oxidase, subunit 2 | |
CNHFAHCC_06316 | 1.1e-24 | S | Domain of Unknown Function (DUF1540) | |||
CNHFAHCC_06317 | 1.4e-151 | troD | P | 'COG1108 ABC-type Mn2 Zn2 transport systems, permease components' | ||
CNHFAHCC_06318 | 3.2e-234 | mntC | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
CNHFAHCC_06319 | 1.2e-140 | mntB | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
CNHFAHCC_06320 | 1.8e-170 | troA | P | Belongs to the bacterial solute-binding protein 9 family | ||
CNHFAHCC_06321 | 1.4e-214 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
CNHFAHCC_06322 | 2.4e-278 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
CNHFAHCC_06323 | 4.2e-155 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
CNHFAHCC_06324 | 3.8e-156 | menH | 4.2.99.20 | S | Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) | |
CNHFAHCC_06325 | 0.0 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
CNHFAHCC_06326 | 8.5e-273 | menF | 5.4.4.2 | HQ | Isochorismate synthase | |
CNHFAHCC_06327 | 2.6e-132 | dksA | T | COG1734 DnaK suppressor protein | ||
CNHFAHCC_06328 | 1e-153 | galU | 2.7.7.9 | M | Nucleotidyl transferase | |
CNHFAHCC_06329 | 1.5e-244 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
CNHFAHCC_06330 | 3.9e-181 | ytcB | 5.1.3.2 | M | NAD-dependent epimerase dehydratase | |
CNHFAHCC_06331 | 3.6e-235 | ytcC | M | Glycosyltransferase Family 4 | ||
CNHFAHCC_06333 | 2.3e-206 | cotS | S | Seems to be required for the assembly of the CotSA protein in spores | ||
CNHFAHCC_06334 | 1.8e-217 | cotSA | M | Glycosyl transferases group 1 | ||
CNHFAHCC_06335 | 1.8e-206 | cotI | S | Spore coat protein | ||
CNHFAHCC_06336 | 9.9e-77 | tspO | T | membrane | ||
CNHFAHCC_06337 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
CNHFAHCC_06338 | 4.3e-288 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
CNHFAHCC_06339 | 1.3e-177 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Glucose-1-phosphate adenylyltransferase, GlgD subunit |
CNHFAHCC_06340 | 3.6e-197 | glgC | 2.7.7.27 | G | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
CNHFAHCC_06341 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
CNHFAHCC_06350 | 7.8e-08 | |||||
CNHFAHCC_06351 | 1.3e-09 | |||||
CNHFAHCC_06358 | 2e-08 | |||||
CNHFAHCC_06364 | 2e-08 | |||||
CNHFAHCC_06369 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
CNHFAHCC_06370 | 4.3e-90 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
CNHFAHCC_06371 | 3.4e-94 | M1-753 | M | FR47-like protein | ||
CNHFAHCC_06372 | 4.1e-188 | yuaG | 3.4.21.72 | S | protein conserved in bacteria | |
CNHFAHCC_06373 | 1.4e-77 | yuaF | OU | Membrane protein implicated in regulation of membrane protease activity | ||
CNHFAHCC_06374 | 3.9e-84 | yuaE | S | DinB superfamily | ||
CNHFAHCC_06375 | 7.9e-108 | yuaD | ||||
CNHFAHCC_06376 | 2.9e-229 | gbsB | 1.1.1.1 | C | alcohol dehydrogenase | |
CNHFAHCC_06377 | 8e-282 | gbsA | 1.2.1.8 | C | Belongs to the aldehyde dehydrogenase family | |
CNHFAHCC_06378 | 1.1e-95 | yuaC | K | Belongs to the GbsR family | ||
CNHFAHCC_06379 | 2.2e-91 | yuaB | ||||
CNHFAHCC_06380 | 5e-122 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
CNHFAHCC_06381 | 5.4e-237 | ktrB | P | Potassium | ||
CNHFAHCC_06382 | 1e-38 | yiaA | S | yiaA/B two helix domain | ||
CNHFAHCC_06383 | 6.4e-153 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
CNHFAHCC_06384 | 6.2e-277 | yubD | P | Major Facilitator Superfamily | ||
CNHFAHCC_06385 | 2.6e-88 | cdoA | 1.13.11.20 | S | Cysteine dioxygenase type I | |
CNHFAHCC_06387 | 1.2e-133 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
CNHFAHCC_06388 | 6.3e-197 | yubA | S | transporter activity | ||
CNHFAHCC_06389 | 3.3e-183 | ygjR | S | Oxidoreductase | ||
CNHFAHCC_06390 | 1.4e-253 | rhaA | 2.7.1.5, 5.3.1.14 | G | Belongs to the rhamnose isomerase family | |
CNHFAHCC_06391 | 6.9e-52 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
CNHFAHCC_06392 | 1.3e-281 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | G | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
CNHFAHCC_06393 | 1e-134 | fucR | K | COG1349 Transcriptional regulators of sugar metabolism | ||
CNHFAHCC_06394 | 0.0 | rhaD | 1.1.1.1, 4.1.2.19 | IQ | Class II Aldolase and Adducin N-terminal domain | |
CNHFAHCC_06395 | 5.1e-239 | mcpA | NT | chemotaxis protein | ||
CNHFAHCC_06396 | 2.2e-295 | mcpA | NT | chemotaxis protein | ||
CNHFAHCC_06397 | 1.5e-222 | mcpA | NT | chemotaxis protein | ||
CNHFAHCC_06398 | 3.2e-225 | mcpA | NT | chemotaxis protein | ||
CNHFAHCC_06399 | 2.6e-140 | tgl | 2.3.2.13 | S | protein-glutamine gamma-glutamyltransferase activity | |
CNHFAHCC_06400 | 1.5e-34 | |||||
CNHFAHCC_06401 | 2.1e-72 | yugU | S | Uncharacterised protein family UPF0047 | ||
CNHFAHCC_06402 | 0.0 | yugT | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | COG0366 Glycosidases |
CNHFAHCC_06403 | 2.6e-236 | yugS | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
CNHFAHCC_06404 | 1.4e-116 | yugP | S | Zn-dependent protease | ||
CNHFAHCC_06405 | 4.6e-39 | |||||
CNHFAHCC_06406 | 1.1e-53 | mstX | S | Membrane-integrating protein Mistic | ||
CNHFAHCC_06407 | 1.7e-182 | yugO | P | COG1226 Kef-type K transport systems | ||
CNHFAHCC_06408 | 1.3e-72 | yugN | S | YugN-like family | ||
CNHFAHCC_06410 | 1.6e-260 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
CNHFAHCC_06411 | 2.8e-229 | yugK | C | Dehydrogenase | ||
CNHFAHCC_06412 | 8.9e-228 | yugJ | C | oxidoreductases, Fe-dependent alcohol dehydrogenase family | ||
CNHFAHCC_06413 | 1.1e-34 | yuzA | S | Domain of unknown function (DUF378) | ||
CNHFAHCC_06414 | 8.9e-63 | yugI | 5.3.1.9 | J | RNA binding protein (contains ribosomal protein S1 domain) | |
CNHFAHCC_06415 | 1.7e-215 | yugH | 2.6.1.1 | E | Aminotransferase | |
CNHFAHCC_06416 | 1.6e-85 | alaR | K | Transcriptional regulator | ||
CNHFAHCC_06417 | 1e-156 | yugF | I | Hydrolase | ||
CNHFAHCC_06418 | 9.8e-42 | yugE | S | Domain of unknown function (DUF1871) | ||
CNHFAHCC_06419 | 1.8e-228 | patB | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
CNHFAHCC_06420 | 4.6e-233 | T | PhoQ Sensor | |||
CNHFAHCC_06421 | 2e-70 | kapB | G | Kinase associated protein B | ||
CNHFAHCC_06422 | 1.9e-115 | kapD | L | the KinA pathway to sporulation | ||
CNHFAHCC_06424 | 3.5e-186 | yuxJ | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06425 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin-binding Protein |
CNHFAHCC_06426 | 6.3e-75 | yuxK | S | protein conserved in bacteria | ||
CNHFAHCC_06427 | 6.3e-78 | yufK | S | Family of unknown function (DUF5366) | ||
CNHFAHCC_06428 | 9.9e-294 | dcuS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
CNHFAHCC_06429 | 2.3e-125 | dcuR | T | COG4565 Response regulator of citrate malate metabolism | ||
CNHFAHCC_06430 | 2.5e-192 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
CNHFAHCC_06431 | 1.1e-273 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
CNHFAHCC_06432 | 6.5e-185 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
CNHFAHCC_06433 | 4.5e-169 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
CNHFAHCC_06434 | 1.3e-233 | maeN | C | COG3493 Na citrate symporter | ||
CNHFAHCC_06435 | 1.9e-14 | |||||
CNHFAHCC_06436 | 0.0 | phaA | 1.6.5.3 | CP | COG1009 NADH ubiquinone oxidoreductase subunit 5 (chain L) Multisubunit Na H antiporter, MnhA subunit | |
CNHFAHCC_06437 | 5.4e-69 | mrpB | P | Subunit B of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
CNHFAHCC_06438 | 1.5e-50 | phaC | 1.6.5.3 | P | Subunit C of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | |
CNHFAHCC_06439 | 3.8e-263 | mrpD | CP | Subunit D of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
CNHFAHCC_06440 | 4.8e-79 | mrpE | P | Subunit E of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
CNHFAHCC_06441 | 7.2e-38 | phaF | P | Subunit F of antiporter complex involved in resistance to high concentrations of Na , K , Li and or alkali | ||
CNHFAHCC_06442 | 5.2e-60 | phaG | P | COG1320 Multisubunit Na H antiporter, MnhG subunit | ||
CNHFAHCC_06443 | 9.7e-65 | ydiI | Q | protein, possibly involved in aromatic compounds catabolism | ||
CNHFAHCC_06444 | 5.1e-116 | comA | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_06445 | 0.0 | comP | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_06447 | 2.5e-162 | comQ | H | Polyprenyl synthetase | ||
CNHFAHCC_06449 | 1.1e-22 | yuzC | ||||
CNHFAHCC_06450 | 2.2e-232 | yuxH | 3.1.4.52 | T | signal transduction protein containing EAL and modified HD-GYP domains | |
CNHFAHCC_06451 | 3.6e-266 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
CNHFAHCC_06452 | 2.9e-104 | pncA | Q | COG1335 Amidases related to nicotinamidase | ||
CNHFAHCC_06453 | 1.6e-67 | yueI | S | Protein of unknown function (DUF1694) | ||
CNHFAHCC_06454 | 7.4e-39 | yueH | S | YueH-like protein | ||
CNHFAHCC_06455 | 2.1e-32 | yueG | S | Spore germination protein gerPA/gerPF | ||
CNHFAHCC_06456 | 1.9e-190 | yueF | S | transporter activity | ||
CNHFAHCC_06457 | 6.1e-72 | S | Protein of unknown function (DUF2283) | |||
CNHFAHCC_06458 | 2.9e-24 | S | Protein of unknown function (DUF2642) | |||
CNHFAHCC_06459 | 4.8e-96 | yueE | S | phosphohydrolase | ||
CNHFAHCC_06460 | 4.4e-132 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_06461 | 5.4e-65 | yueC | S | Family of unknown function (DUF5383) | ||
CNHFAHCC_06462 | 0.0 | esaA | S | type VII secretion protein EsaA | ||
CNHFAHCC_06463 | 0.0 | essC | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
CNHFAHCC_06464 | 2.3e-211 | essB | S | WXG100 protein secretion system (Wss), protein YukC | ||
CNHFAHCC_06465 | 7.7e-41 | yukD | S | WXG100 protein secretion system (Wss), protein YukD | ||
CNHFAHCC_06466 | 2.8e-45 | esxA | S | Belongs to the WXG100 family | ||
CNHFAHCC_06467 | 1.5e-228 | yukF | QT | Transcriptional regulator | ||
CNHFAHCC_06468 | 1.2e-205 | ald | 1.4.1.1 | E | Belongs to the AlaDH PNT family | |
CNHFAHCC_06469 | 1.1e-132 | yukJ | S | Uncharacterized conserved protein (DUF2278) | ||
CNHFAHCC_06470 | 3.8e-36 | mbtH | S | MbtH-like protein | ||
CNHFAHCC_06471 | 0.0 | dhbF | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | ||
CNHFAHCC_06472 | 1.4e-178 | entB | 3.3.2.1, 6.3.2.14 | Q | Isochorismatase family | |
CNHFAHCC_06473 | 0.0 | entE | 2.7.7.58, 6.3.2.14 | Q | 2,3-dihydroxybenzoate-AMP ligase | |
CNHFAHCC_06474 | 2.3e-226 | entC | 5.4.4.2 | HQ | Isochorismate synthase | |
CNHFAHCC_06475 | 7.3e-141 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_06476 | 1.3e-167 | besA | S | Putative esterase | ||
CNHFAHCC_06477 | 5.8e-122 | yuiH | S | Oxidoreductase molybdopterin binding domain | ||
CNHFAHCC_06478 | 1.1e-93 | bioY | S | Biotin biosynthesis protein | ||
CNHFAHCC_06479 | 3.9e-211 | yuiF | S | antiporter | ||
CNHFAHCC_06480 | 1.5e-280 | pepA | 3.4.11.1, 3.4.11.5 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
CNHFAHCC_06481 | 1.2e-77 | yuiD | S | protein conserved in bacteria | ||
CNHFAHCC_06482 | 9.5e-118 | yuiC | S | protein conserved in bacteria | ||
CNHFAHCC_06483 | 8.4e-27 | yuiB | S | Putative membrane protein | ||
CNHFAHCC_06484 | 2.5e-236 | yumB | 1.6.99.3 | C | NADH dehydrogenase | |
CNHFAHCC_06485 | 3.5e-188 | yumC | 1.18.1.2, 1.19.1.1 | C | reductase | |
CNHFAHCC_06487 | 4.9e-187 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
CNHFAHCC_06488 | 1.2e-117 | paiB | K | Putative FMN-binding domain | ||
CNHFAHCC_06489 | 4.7e-72 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
CNHFAHCC_06490 | 3.7e-63 | erpA | S | Belongs to the HesB IscA family | ||
CNHFAHCC_06491 | 2.2e-162 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
CNHFAHCC_06492 | 2.4e-199 | yutK | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
CNHFAHCC_06493 | 3.2e-39 | yuzB | S | Belongs to the UPF0349 family | ||
CNHFAHCC_06494 | 1.2e-199 | yutJ | 1.6.99.3 | C | NADH dehydrogenase | |
CNHFAHCC_06495 | 3.5e-57 | yuzD | S | protein conserved in bacteria | ||
CNHFAHCC_06496 | 1.2e-35 | yutI | O | COG0694 Thioredoxin-like proteins and domains | ||
CNHFAHCC_06497 | 0.0 | yuxL | 3.4.14.5, 3.4.19.1 | EU | peptidase | |
CNHFAHCC_06498 | 8.6e-173 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
CNHFAHCC_06499 | 2.3e-198 | thrC | 4.2.3.1 | E | Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine | |
CNHFAHCC_06500 | 2.7e-241 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
CNHFAHCC_06501 | 2e-199 | yutH | S | Spore coat protein | ||
CNHFAHCC_06502 | 5.6e-86 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
CNHFAHCC_06503 | 6.5e-142 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
CNHFAHCC_06504 | 1e-75 | yutE | S | Protein of unknown function DUF86 | ||
CNHFAHCC_06505 | 9.7e-48 | yutD | S | protein conserved in bacteria | ||
CNHFAHCC_06506 | 4.9e-111 | yutC | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
CNHFAHCC_06507 | 1e-167 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
CNHFAHCC_06508 | 2.1e-196 | lytH | M | Peptidase, M23 | ||
CNHFAHCC_06509 | 8.4e-134 | yunB | S | Sporulation protein YunB (Spo_YunB) | ||
CNHFAHCC_06510 | 5.1e-48 | yunC | S | Domain of unknown function (DUF1805) | ||
CNHFAHCC_06511 | 5.8e-266 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
CNHFAHCC_06512 | 2e-141 | yunE | S | membrane transporter protein | ||
CNHFAHCC_06513 | 5.7e-171 | yunF | S | Protein of unknown function DUF72 | ||
CNHFAHCC_06514 | 3e-62 | yunG | ||||
CNHFAHCC_06515 | 1e-259 | allB | 3.5.2.5 | F | Catalyzes the conversion of allantoin (5- ureidohydantoin) to allantoic acid by hydrolytic cleavage of the five-member hydantoin ring | |
CNHFAHCC_06516 | 1.2e-302 | pucR | QT | COG2508 Regulator of polyketide synthase expression | ||
CNHFAHCC_06517 | 2.1e-236 | pbuX | F | Permease family | ||
CNHFAHCC_06518 | 1.3e-224 | pbuX | F | xanthine | ||
CNHFAHCC_06519 | 6.6e-284 | uraD | 1.7.3.3, 3.5.1.41, 4.1.1.97 | Q | Catalyzes the oxidation of uric acid to 5- hydroxyisourate, which is further processed to form (S)-allantoin | |
CNHFAHCC_06520 | 7.3e-61 | uraH | 3.5.2.17, 4.1.1.97 | S | Belongs to the transthyretin family. 5-hydroxyisourate hydrolase subfamily | |
CNHFAHCC_06522 | 7.9e-99 | 1.17.1.4, 1.2.5.3, 1.3.99.16 | C | COG2080 Aerobic-type carbon monoxide dehydrogenase, small subunit CoxS CutS homologs | ||
CNHFAHCC_06523 | 0.0 | xdhA | 1.17.1.4 | C | COG1529 Aerobic-type carbon monoxide dehydrogenase, large subunit CoxL CutL homologs | |
CNHFAHCC_06524 | 3.4e-152 | ygfM | 1.17.1.4, 1.2.5.3 | C | COG1319 Aerobic-type carbon monoxide dehydrogenase, middle subunit CoxM CutM homologs | |
CNHFAHCC_06525 | 3.6e-111 | pucB | 1.1.1.328, 1.17.1.4, 2.7.7.76 | S | MobA-like NTP transferase domain | |
CNHFAHCC_06526 | 1.7e-190 | pucA | 1.17.1.4 | O | COG1975 Xanthine and CO dehydrogenases maturation factor, XdhC CoxF family | |
CNHFAHCC_06527 | 1.9e-239 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | COG0075 Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
CNHFAHCC_06528 | 1.6e-238 | pucF | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | COG0624 Acetylornithine deacetylase Succinyl-diaminopimelate desuccinylase and related deacylases | |
CNHFAHCC_06529 | 2.4e-169 | bsn | L | Ribonuclease | ||
CNHFAHCC_06530 | 1.2e-205 | msmX | P | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_06531 | 1.1e-135 | yurK | K | UTRA | ||
CNHFAHCC_06532 | 1.5e-163 | yurL | 2.7.1.218 | G | pfkB family carbohydrate kinase | |
CNHFAHCC_06533 | 7.3e-169 | yurM | P | COG0395 ABC-type sugar transport system, permease component | ||
CNHFAHCC_06534 | 1.4e-156 | yurN | G | Binding-protein-dependent transport system inner membrane component | ||
CNHFAHCC_06535 | 1.3e-240 | yurO | G | COG1653 ABC-type sugar transport system, periplasmic component | ||
CNHFAHCC_06536 | 1.8e-184 | frlB | M | Catalyzes the conversion of a range of fructosamine 6- phosphates to glucose 6-phosphate and a free amino acid | ||
CNHFAHCC_06537 | 2.8e-66 | yurQ | 2.7.7.7 | L | COG0322 Nuclease subunit of the excinuclease complex | |
CNHFAHCC_06538 | 1.8e-209 | yurR | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
CNHFAHCC_06540 | 1e-41 | |||||
CNHFAHCC_06541 | 7.6e-67 | yurT | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
CNHFAHCC_06542 | 3.3e-43 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
CNHFAHCC_06543 | 3.5e-271 | sufB | O | FeS cluster assembly | ||
CNHFAHCC_06544 | 1.4e-77 | nifU | C | COG0822 NifU homolog involved in Fe-S cluster formation | ||
CNHFAHCC_06545 | 9.4e-236 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
CNHFAHCC_06546 | 1.4e-245 | sufD | O | assembly protein SufD | ||
CNHFAHCC_06547 | 2.3e-142 | sufC | O | COG0396 ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
CNHFAHCC_06548 | 1.4e-65 | yurZ | 2.3.1.12, 4.1.1.44 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |
CNHFAHCC_06549 | 1.9e-147 | metQ | P | Belongs to the NlpA lipoprotein family | ||
CNHFAHCC_06550 | 1.4e-95 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
CNHFAHCC_06551 | 5.2e-185 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
CNHFAHCC_06552 | 2.4e-56 | yusD | S | SCP-2 sterol transfer family | ||
CNHFAHCC_06553 | 5.6e-55 | traF | CO | Thioredoxin | ||
CNHFAHCC_06554 | 3.3e-74 | rnmV | 3.1.26.8 | L | COG1658 Small primase-like proteins (Toprim domain) | |
CNHFAHCC_06555 | 1.1e-39 | yusG | S | Protein of unknown function (DUF2553) | ||
CNHFAHCC_06556 | 9.3e-65 | gcvH | E | Is also involved in protein lipoylation via its role as an octanoyl lipoyl carrier protein intermediate | ||
CNHFAHCC_06557 | 2.8e-63 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
CNHFAHCC_06558 | 0.0 | fadE | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
CNHFAHCC_06559 | 1.4e-217 | fadA | 2.3.1.16 | I | Belongs to the thiolase family | |
CNHFAHCC_06560 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
CNHFAHCC_06561 | 4.7e-09 | S | YuzL-like protein | |||
CNHFAHCC_06562 | 2.2e-165 | fadM | E | Proline dehydrogenase | ||
CNHFAHCC_06563 | 5.1e-40 | |||||
CNHFAHCC_06564 | 3.2e-53 | yusN | M | Coat F domain | ||
CNHFAHCC_06565 | 5.4e-75 | yusO | K | Iron dependent repressor, N-terminal DNA binding domain | ||
CNHFAHCC_06566 | 3.8e-293 | yusP | P | Major facilitator superfamily | ||
CNHFAHCC_06567 | 8.4e-66 | yusQ | S | Tautomerase enzyme | ||
CNHFAHCC_06568 | 2.7e-55 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_06569 | 2.5e-50 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_06570 | 2.7e-160 | yusT | K | LysR substrate binding domain | ||
CNHFAHCC_06571 | 5.6e-39 | yusU | S | Protein of unknown function (DUF2573) | ||
CNHFAHCC_06572 | 1e-153 | yusV | 3.6.3.34 | HP | ABC transporter | |
CNHFAHCC_06573 | 5.6e-66 | S | YusW-like protein | |||
CNHFAHCC_06574 | 6.3e-258 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
CNHFAHCC_06575 | 3.9e-34 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
CNHFAHCC_06576 | 4.7e-154 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_06577 | 1.2e-79 | dps | P | Ferritin-like domain | ||
CNHFAHCC_06578 | 9.6e-237 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
CNHFAHCC_06579 | 3.4e-126 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_06580 | 4.3e-250 | cssS | 2.7.13.3 | T | PhoQ Sensor | |
CNHFAHCC_06581 | 2.1e-158 | yuxN | K | Transcriptional regulator | ||
CNHFAHCC_06582 | 2.5e-261 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
CNHFAHCC_06583 | 2.3e-24 | S | Protein of unknown function (DUF3970) | |||
CNHFAHCC_06584 | 2.2e-247 | gerAA | EG | Spore germination protein | ||
CNHFAHCC_06585 | 9.1e-198 | gerAB | E | Spore germination protein | ||
CNHFAHCC_06586 | 4.6e-189 | gerAC | S | Spore germination B3/ GerAC like, C-terminal | ||
CNHFAHCC_06587 | 1.3e-108 | vraR | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_06588 | 5.5e-187 | vraS | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_06589 | 5.6e-127 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
CNHFAHCC_06590 | 9.3e-129 | liaG | S | Putative adhesin | ||
CNHFAHCC_06591 | 2.5e-105 | liaH | KT | COG1842 Phage shock protein A (IM30), suppresses sigma54-dependent transcription | ||
CNHFAHCC_06592 | 5.6e-62 | liaI | S | membrane | ||
CNHFAHCC_06593 | 4.8e-227 | yvqJ | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06594 | 6.5e-102 | yvqK | 2.5.1.17 | S | Adenosyltransferase | |
CNHFAHCC_06595 | 2.8e-249 | yvrA | 3.6.3.34 | HP | COG1120 ABC-type cobalamin Fe3 -siderophores transport systems, ATPase components | |
CNHFAHCC_06596 | 1.3e-171 | btuC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_06597 | 1.8e-170 | yvrC | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
CNHFAHCC_06598 | 6.2e-140 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_06599 | 1.5e-171 | yvrE | G | SMP-30/Gluconolaconase/LRE-like region | ||
CNHFAHCC_06600 | 0.0 | T | PhoQ Sensor | |||
CNHFAHCC_06601 | 3.8e-131 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_06602 | 3.6e-22 | |||||
CNHFAHCC_06603 | 1.8e-96 | yvrI | K | RNA polymerase | ||
CNHFAHCC_06604 | 2.4e-19 | S | YvrJ protein family | |||
CNHFAHCC_06605 | 7.3e-230 | oxdC | 4.1.1.2 | G | Oxalate decarboxylase | |
CNHFAHCC_06606 | 1.3e-64 | yvrL | S | Regulatory protein YrvL | ||
CNHFAHCC_06607 | 1.8e-210 | yvrN | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
CNHFAHCC_06608 | 7.1e-124 | macB | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_06609 | 4.8e-176 | M | Efflux transporter rnd family, mfp subunit | |||
CNHFAHCC_06610 | 4.4e-149 | fhuC | 3.6.3.34 | HP | ABC transporter | |
CNHFAHCC_06611 | 5.3e-176 | fhuG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_06612 | 5.4e-204 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
CNHFAHCC_06613 | 2.1e-179 | fhuD | P | ABC transporter | ||
CNHFAHCC_06615 | 2.6e-237 | yvsH | E | Arginine ornithine antiporter | ||
CNHFAHCC_06616 | 6.5e-16 | S | Small spore protein J (Spore_SspJ) | |||
CNHFAHCC_06617 | 1e-84 | yvsG | S | LexA-binding, inner membrane-associated putative hydrolase | ||
CNHFAHCC_06618 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
CNHFAHCC_06619 | 8e-171 | yvgK | P | COG1910 Periplasmic molybdate-binding protein domain | ||
CNHFAHCC_06620 | 5.8e-138 | modA | P | COG0725 ABC-type molybdate transport system, periplasmic component | ||
CNHFAHCC_06621 | 4.7e-120 | modB | P | COG4149 ABC-type molybdate transport system, permease component | ||
CNHFAHCC_06622 | 9.1e-158 | yvgN | S | reductase | ||
CNHFAHCC_06623 | 5.4e-86 | yvgO | ||||
CNHFAHCC_06624 | 0.0 | yjcE | P | COG0025 NhaP-type Na H and K H antiporters | ||
CNHFAHCC_06625 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate | |
CNHFAHCC_06626 | 0.0 | cysJ | 1.8.1.2 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component | |
CNHFAHCC_06627 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
CNHFAHCC_06628 | 4.1e-107 | yvgT | S | membrane | ||
CNHFAHCC_06629 | 2.2e-72 | bdbC | O | Required for disulfide bond formation in some proteins | ||
CNHFAHCC_06630 | 1.6e-104 | bdbD | O | Thioredoxin | ||
CNHFAHCC_06631 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
CNHFAHCC_06632 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
CNHFAHCC_06633 | 1.5e-29 | copZ | P | Copper resistance protein CopZ | ||
CNHFAHCC_06634 | 2.2e-48 | csoR | S | transcriptional | ||
CNHFAHCC_06635 | 2.1e-199 | yvaA | 1.1.1.371 | S | Oxidoreductase | |
CNHFAHCC_06636 | 2.4e-118 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
CNHFAHCC_06637 | 0.0 | yvaC | S | Fusaric acid resistance protein-like | ||
CNHFAHCC_06638 | 5.7e-73 | yvaD | S | Family of unknown function (DUF5360) | ||
CNHFAHCC_06639 | 2.8e-55 | yvaE | P | Small Multidrug Resistance protein | ||
CNHFAHCC_06640 | 4.1e-101 | K | Bacterial regulatory proteins, tetR family | |||
CNHFAHCC_06641 | 9.1e-131 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_06643 | 1.6e-82 | smpB | O | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | ||
CNHFAHCC_06644 | 0.0 | rnr | K | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
CNHFAHCC_06645 | 5.6e-143 | est | 3.1.1.1 | S | Carboxylesterase | |
CNHFAHCC_06646 | 2.4e-23 | secG | U | Preprotein translocase subunit SecG | ||
CNHFAHCC_06647 | 3.7e-153 | yvaM | S | Serine aminopeptidase, S33 | ||
CNHFAHCC_06648 | 7.5e-36 | yvzC | K | Transcriptional | ||
CNHFAHCC_06649 | 4e-69 | K | transcriptional | |||
CNHFAHCC_06650 | 8e-70 | yvaO | K | Cro/C1-type HTH DNA-binding domain | ||
CNHFAHCC_06651 | 2.2e-54 | yodB | K | transcriptional | ||
CNHFAHCC_06652 | 4.2e-226 | NT | chemotaxis protein | |||
CNHFAHCC_06653 | 8.1e-112 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
CNHFAHCC_06654 | 1.1e-172 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
CNHFAHCC_06655 | 2.5e-110 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
CNHFAHCC_06656 | 3e-212 | opuCA | 3.6.3.32 | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | |
CNHFAHCC_06657 | 8.8e-61 | yvbF | K | Belongs to the GbsR family | ||
CNHFAHCC_06658 | 7.9e-13 | S | Sporulation delaying protein SdpA | |||
CNHFAHCC_06659 | 7.6e-172 | |||||
CNHFAHCC_06660 | 4.4e-08 | |||||
CNHFAHCC_06661 | 3.3e-96 | sdpI | S | Immunity protein that provides protection for the cell against the toxic effects of SDP, its own SdpC-derived killing factor, and that functions as a receptor signal transduction protein as well. Once SDP accumulates in the extracellular milieu, SdpI binds to SDP, causing sequestration of SdpR at the bacterial membrane | ||
CNHFAHCC_06662 | 4.5e-45 | sdpR | K | transcriptional | ||
CNHFAHCC_06663 | 8.7e-114 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
CNHFAHCC_06664 | 2.5e-172 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
CNHFAHCC_06665 | 4.5e-112 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
CNHFAHCC_06666 | 8.8e-212 | opuCA | 3.6.3.32 | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | |
CNHFAHCC_06667 | 1.4e-98 | yvbF | K | Belongs to the GbsR family | ||
CNHFAHCC_06668 | 6.4e-103 | yvbG | U | UPF0056 membrane protein | ||
CNHFAHCC_06669 | 8.6e-113 | yvbH | S | YvbH-like oligomerisation region | ||
CNHFAHCC_06670 | 4.2e-124 | exoY | M | Membrane | ||
CNHFAHCC_06671 | 0.0 | tcaA | S | response to antibiotic | ||
CNHFAHCC_06672 | 7.7e-82 | yvbK | 3.1.3.25 | K | acetyltransferase | |
CNHFAHCC_06673 | 8.4e-243 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
CNHFAHCC_06674 | 1.3e-298 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and | |
CNHFAHCC_06675 | 4.3e-138 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
CNHFAHCC_06676 | 1e-218 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
CNHFAHCC_06677 | 6.2e-185 | gapA | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
CNHFAHCC_06678 | 6.3e-185 | cggR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
CNHFAHCC_06679 | 1.6e-252 | araE | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06680 | 5.5e-203 | araR | K | transcriptional | ||
CNHFAHCC_06681 | 1.5e-191 | yvbT | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_06682 | 3.9e-159 | yvbU | K | Transcriptional regulator | ||
CNHFAHCC_06683 | 8.5e-157 | yvbV | EG | EamA-like transporter family | ||
CNHFAHCC_06684 | 2.8e-241 | yvbW | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
CNHFAHCC_06685 | 4.3e-197 | yvbX | S | Glycosyl hydrolase | ||
CNHFAHCC_06686 | 2.3e-133 | lutC | S | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
CNHFAHCC_06687 | 1.2e-274 | lutB | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. Has probably a role as an electron transporter during oxidation of L-lactate | ||
CNHFAHCC_06688 | 1.5e-137 | lutA | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
CNHFAHCC_06689 | 2.6e-106 | desR | T | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_06690 | 8.9e-201 | desK | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_06691 | 6.2e-134 | yvfS | V | COG0842 ABC-type multidrug transport system, permease component | ||
CNHFAHCC_06692 | 3e-162 | yvfR | V | COG1131 ABC-type multidrug transport system, ATPase component | ||
CNHFAHCC_06693 | 2.6e-157 | rsbQ | S | Alpha/beta hydrolase family | ||
CNHFAHCC_06694 | 1.4e-199 | rsbU | 3.1.3.3 | T | response regulator | |
CNHFAHCC_06695 | 1.6e-252 | galA | 3.2.1.89 | G | arabinogalactan | |
CNHFAHCC_06696 | 0.0 | lacA | 3.2.1.23 | G | beta-galactosidase | |
CNHFAHCC_06697 | 3.2e-150 | ganQ | P | transport | ||
CNHFAHCC_06698 | 1.3e-232 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
CNHFAHCC_06699 | 1.4e-226 | cycB | G | COG2182 Maltose-binding periplasmic proteins domains | ||
CNHFAHCC_06700 | 1.8e-184 | lacR | K | Transcriptional regulator | ||
CNHFAHCC_06701 | 6.6e-111 | yvfI | K | COG2186 Transcriptional regulators | ||
CNHFAHCC_06702 | 1.4e-309 | yvfH | C | L-lactate permease | ||
CNHFAHCC_06703 | 6.5e-243 | rpoN | K | COG1508 DNA-directed RNA polymerase specialized sigma subunit, sigma54 homolog | ||
CNHFAHCC_06704 | 1e-31 | yvfG | S | YvfG protein | ||
CNHFAHCC_06705 | 5.8e-188 | yvfF | GM | Exopolysaccharide biosynthesis protein | ||
CNHFAHCC_06706 | 1.2e-224 | epsN | 2.6.1.102 | E | Belongs to the DegT DnrJ EryC1 family | |
CNHFAHCC_06707 | 2.2e-58 | epsM | GM | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
CNHFAHCC_06708 | 1.1e-46 | epsL | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
CNHFAHCC_06709 | 1.2e-35 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
CNHFAHCC_06710 | 3.6e-19 | IFNB1 | T | Interferon alpha, beta and delta. | ||
CNHFAHCC_06711 | 1.6e-81 | S | KNTase C-terminal domain | |||
CNHFAHCC_06712 | 1.4e-195 | epsF | GT4 | M | Glycosyl transferases group 1 | |
CNHFAHCC_06713 | 4.1e-158 | epsE | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
CNHFAHCC_06714 | 2e-224 | epsD | GT4 | M | Glycosyl transferase 4-like | |
CNHFAHCC_06715 | 0.0 | pglF | 4.2.1.115, 4.2.1.135, 4.2.1.46 | GM | Polysaccharide biosynthesis protein | |
CNHFAHCC_06716 | 1e-114 | epsB | 2.7.10.2 | D | COG0489 ATPases involved in chromosome partitioning | |
CNHFAHCC_06717 | 4e-122 | ywqC | M | biosynthesis protein | ||
CNHFAHCC_06718 | 5.7e-77 | slr | K | transcriptional | ||
CNHFAHCC_06719 | 4.8e-287 | pnbA | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
CNHFAHCC_06721 | 4.6e-93 | padC | Q | Phenolic acid decarboxylase | ||
CNHFAHCC_06722 | 1.3e-48 | MA20_18690 | S | Protein of unknown function (DUF3237) | ||
CNHFAHCC_06723 | 3.1e-127 | racX | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
CNHFAHCC_06724 | 9.6e-266 | pbpE | V | Beta-lactamase | ||
CNHFAHCC_06725 | 1.2e-274 | sacB | 2.4.1.10 | GH68 | M | levansucrase activity |
CNHFAHCC_06726 | 0.0 | levB | 3.2.1.26, 3.2.1.64, 3.2.1.65, 3.2.1.80 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
CNHFAHCC_06727 | 1.8e-295 | yveA | E | amino acid | ||
CNHFAHCC_06728 | 2.6e-106 | yvdT | K | Transcriptional regulator | ||
CNHFAHCC_06729 | 6.7e-51 | ykkC | P | Small Multidrug Resistance protein | ||
CNHFAHCC_06730 | 4.1e-50 | sugE | P | Small Multidrug Resistance protein | ||
CNHFAHCC_06731 | 2.2e-93 | yvdQ | S | Protein of unknown function (DUF3231) | ||
CNHFAHCC_06732 | 8.4e-270 | ygaK | C | COG0277 FAD FMN-containing dehydrogenases | ||
CNHFAHCC_06733 | 1.5e-183 | S | Patatin-like phospholipase | |||
CNHFAHCC_06735 | 1.2e-103 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
CNHFAHCC_06736 | 1.3e-122 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
CNHFAHCC_06737 | 0.0 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
CNHFAHCC_06738 | 0.0 | yvdK | 2.4.1.8 | GH65 | G | Glycoside hydrolase, family 65 |
CNHFAHCC_06739 | 1.2e-158 | malA | S | Protein of unknown function (DUF1189) | ||
CNHFAHCC_06740 | 7.8e-149 | malD | P | transport | ||
CNHFAHCC_06741 | 5.3e-245 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
CNHFAHCC_06742 | 3.7e-235 | mdxE | G | COG2182 Maltose-binding periplasmic proteins domains | ||
CNHFAHCC_06743 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha amylase, N-terminal ig-like domain |
CNHFAHCC_06744 | 3.6e-174 | yvdE | K | Transcriptional regulator | ||
CNHFAHCC_06745 | 3.3e-106 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
CNHFAHCC_06746 | 6.8e-53 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
CNHFAHCC_06747 | 2.1e-288 | sulP | P | COG0659 Sulfate permease and related transporters (MFS superfamily) | ||
CNHFAHCC_06748 | 5.7e-106 | ytiB | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
CNHFAHCC_06749 | 1.3e-184 | ghrB | 1.1.1.215, 1.1.1.26, 1.1.1.43, 1.1.1.79, 1.1.1.81 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
CNHFAHCC_06750 | 0.0 | yxdM | V | ABC transporter (permease) | ||
CNHFAHCC_06751 | 5.6e-141 | yvcR | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_06752 | 2.3e-198 | yvcQ | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
CNHFAHCC_06753 | 3.9e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_06754 | 1.8e-33 | |||||
CNHFAHCC_06755 | 8.6e-147 | nhoA | 2.3.1.118 | Q | Belongs to the arylamine N-acetyltransferase family | |
CNHFAHCC_06756 | 1.6e-36 | crh | G | Phosphocarrier protein Chr | ||
CNHFAHCC_06757 | 1.4e-170 | whiA | K | May be required for sporulation | ||
CNHFAHCC_06758 | 7.3e-178 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
CNHFAHCC_06759 | 5.7e-166 | rapZ | S | Displays ATPase and GTPase activities | ||
CNHFAHCC_06760 | 1.8e-89 | yvcI | 3.6.1.55 | F | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
CNHFAHCC_06761 | 1.4e-175 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
CNHFAHCC_06762 | 1.4e-102 | usp | CBM50 | M | protein conserved in bacteria | |
CNHFAHCC_06763 | 2.4e-278 | S | COG0457 FOG TPR repeat | |||
CNHFAHCC_06764 | 0.0 | msbA2 | 3.6.3.44 | V | ABC transporter | |
CNHFAHCC_06766 | 0.0 | |||||
CNHFAHCC_06767 | 4.6e-121 | |||||
CNHFAHCC_06768 | 8e-114 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | belongs to the PRA-CH family | |
CNHFAHCC_06769 | 2.8e-137 | hisF | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | ||
CNHFAHCC_06770 | 3.1e-133 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
CNHFAHCC_06771 | 1.7e-116 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
CNHFAHCC_06772 | 2.1e-108 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
CNHFAHCC_06773 | 6.6e-232 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
CNHFAHCC_06774 | 1.5e-115 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
CNHFAHCC_06775 | 4.8e-221 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
CNHFAHCC_06776 | 4.5e-140 | yvpB | NU | protein conserved in bacteria | ||
CNHFAHCC_06777 | 5.5e-121 | hrpW | 4.2.2.10, 4.2.2.2 | G | Pectate lyase | |
CNHFAHCC_06778 | 3e-82 | yvoF | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
CNHFAHCC_06779 | 1.3e-119 | ppaX | 3.1.3.18, 3.6.1.1 | S | Hydrolyzes pyrophosphate formed during P-Ser-HPr dephosphorylation by HPrK P. Might play a role in controlling the intracellular pyrophosphate pool | |
CNHFAHCC_06780 | 1.5e-164 | yvoD | P | COG0370 Fe2 transport system protein B | ||
CNHFAHCC_06781 | 4.9e-148 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
CNHFAHCC_06782 | 1.7e-168 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Also phosphorylates dephosphorylates the HPr-like catabolite repression protein crh on a specific serine residue. Therefore, by controlling the phosphorylation state of HPr and crh, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
CNHFAHCC_06783 | 6.8e-223 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
CNHFAHCC_06784 | 8.9e-133 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
CNHFAHCC_06785 | 3.6e-134 | yvoA | K | transcriptional | ||
CNHFAHCC_06786 | 0.0 | yvnB | 3.1.4.53 | Q | Calcineurin-like phosphoesterase | |
CNHFAHCC_06787 | 8.5e-84 | adcR | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_06788 | 8.2e-232 | cypX | 1.14.15.13 | C | Cytochrome P450 | |
CNHFAHCC_06789 | 1.6e-137 | yvmC | 2.3.2.22 | S | Involved in the biosynthesis of pulcherrimin, a red extracellular pigment. It uses activated amino acids in the form of aminoacyl-tRNAs (aa-tRNAs) as substrates to catalyze the ATP- independent formation of cyclodipeptides which are intermediates in diketopiperazine (DKP) biosynthetic pathways. Catalyzes the formation of cyclo(L-Leu-L-Leu) (cLL) from L-leucyl-tRNA(Leu). Can also incorporate various nonpolar residues, such as L- phenylalanine, L-leucine and methionine, into cyclodipeptides | |
CNHFAHCC_06790 | 3e-87 | yvmB | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_06791 | 2.7e-203 | yvmA | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06792 | 1.2e-50 | yvlD | S | Membrane | ||
CNHFAHCC_06793 | 2.6e-26 | pspB | KT | PspC domain | ||
CNHFAHCC_06794 | 3.4e-168 | yvlB | S | Putative adhesin | ||
CNHFAHCC_06795 | 8e-49 | yvlA | ||||
CNHFAHCC_06796 | 6.7e-34 | yvkN | ||||
CNHFAHCC_06797 | 2.9e-79 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
CNHFAHCC_06798 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
CNHFAHCC_06799 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
CNHFAHCC_06800 | 1.2e-30 | csbA | S | protein conserved in bacteria | ||
CNHFAHCC_06801 | 0.0 | yvkC | 2.7.9.2 | GT | Phosphotransferase | |
CNHFAHCC_06803 | 2.7e-94 | yvkB | K | Transcriptional regulator | ||
CNHFAHCC_06804 | 7.9e-228 | yvkA | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06805 | 4.9e-221 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
CNHFAHCC_06806 | 1e-54 | swrA | S | Swarming motility protein | ||
CNHFAHCC_06807 | 6.9e-270 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
CNHFAHCC_06808 | 1.6e-155 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
CNHFAHCC_06809 | 1.6e-123 | ftsE | D | cell division ATP-binding protein FtsE | ||
CNHFAHCC_06810 | 5.3e-56 | cccB | C | COG2010 Cytochrome c, mono- and diheme variants | ||
CNHFAHCC_06811 | 5.5e-142 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
CNHFAHCC_06812 | 6.1e-185 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
CNHFAHCC_06813 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
CNHFAHCC_06814 | 2.2e-102 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
CNHFAHCC_06815 | 2.9e-66 | |||||
CNHFAHCC_06816 | 1.9e-08 | fliT | S | bacterial-type flagellum organization | ||
CNHFAHCC_06817 | 2.9e-69 | fliS | N | flagellar protein FliS | ||
CNHFAHCC_06818 | 1.3e-266 | fliD | N | morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
CNHFAHCC_06819 | 6.1e-57 | flaG | N | flagellar protein FlaG | ||
CNHFAHCC_06820 | 1.9e-156 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
CNHFAHCC_06821 | 2e-30 | csrA | T | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
CNHFAHCC_06822 | 2.7e-73 | fliW | S | Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum | ||
CNHFAHCC_06823 | 2.6e-50 | yviE | ||||
CNHFAHCC_06824 | 1.1e-156 | flgL | N | Belongs to the bacterial flagellin family | ||
CNHFAHCC_06825 | 1.2e-264 | flgK | N | flagellar hook-associated protein | ||
CNHFAHCC_06826 | 2.4e-78 | flgN | NOU | FlgN protein | ||
CNHFAHCC_06827 | 4.2e-40 | flgM | KNU | Negative regulator of flagellin synthesis | ||
CNHFAHCC_06828 | 7e-74 | yvyF | S | flagellar protein | ||
CNHFAHCC_06829 | 2.7e-129 | comFC | S | Phosphoribosyl transferase domain | ||
CNHFAHCC_06830 | 5.7e-46 | comFB | S | Late competence development protein ComFB | ||
CNHFAHCC_06831 | 5.6e-269 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
CNHFAHCC_06832 | 7.3e-155 | degV | S | protein conserved in bacteria | ||
CNHFAHCC_06833 | 2e-126 | degU | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
CNHFAHCC_06834 | 1.9e-182 | degS | 2.7.13.3 | T | Member of the two-component regulatory system DegS DegU, which plays an important role in the transition growth phase | |
CNHFAHCC_06835 | 2e-120 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
CNHFAHCC_06836 | 6e-163 | yvhJ | K | Transcriptional regulator | ||
CNHFAHCC_06837 | 2.6e-181 | tagO | 2.7.8.33, 2.7.8.35 | M | COG0472 UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
CNHFAHCC_06838 | 4.4e-238 | tuaH | M | Teichuronic acid biosynthesis glycosyltransferase tuaH | ||
CNHFAHCC_06839 | 2.1e-145 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
CNHFAHCC_06840 | 6e-115 | tuaF | M | protein involved in exopolysaccharide biosynthesis | ||
CNHFAHCC_06841 | 1.7e-263 | tuaE | M | Teichuronic acid biosynthesis protein | ||
CNHFAHCC_06842 | 2.4e-259 | tuaD | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
CNHFAHCC_06843 | 7.4e-222 | tuaC | 2.4.1.21, 3.2.1.1 | GH13,GT4,GT5 | GM | Teichuronic acid |
CNHFAHCC_06844 | 3.3e-248 | wzxC | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
CNHFAHCC_06845 | 4.6e-112 | tuaA | M | COG2148 Sugar transferases involved in lipopolysaccharide synthesis | ||
CNHFAHCC_06846 | 3e-268 | lytC | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
CNHFAHCC_06847 | 0.0 | lytB | 3.5.1.28 | D | Stage II sporulation protein | |
CNHFAHCC_06848 | 6e-38 | |||||
CNHFAHCC_06849 | 6.1e-163 | lytR | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
CNHFAHCC_06850 | 8.5e-218 | mnaA | 5.1.3.14 | M | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
CNHFAHCC_06851 | 9e-164 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
CNHFAHCC_06852 | 0.0 | ggaB | GT2 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
CNHFAHCC_06853 | 8.1e-257 | ggaA | M | Glycosyltransferase like family 2 | ||
CNHFAHCC_06854 | 2.4e-11 | tagF | 2.7.8.12 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
CNHFAHCC_06856 | 1.6e-100 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
CNHFAHCC_06857 | 1.8e-279 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
CNHFAHCC_06858 | 1.1e-150 | tagG | GM | Transport permease protein | ||
CNHFAHCC_06859 | 0.0 | tagF | 2.7.8.12 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
CNHFAHCC_06860 | 0.0 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferase 1 domain A |
CNHFAHCC_06861 | 5.7e-70 | tagD | 2.7.7.15, 2.7.7.39 | IM | Cytidylyltransferase | |
CNHFAHCC_06862 | 1.8e-144 | tagA | 2.4.1.187 | GT26 | M | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
CNHFAHCC_06863 | 5e-215 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
CNHFAHCC_06864 | 1.2e-260 | |||||
CNHFAHCC_06865 | 7.2e-217 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
CNHFAHCC_06866 | 7.1e-191 | pmi | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
CNHFAHCC_06867 | 3.5e-266 | gerBA | EG | Spore germination protein | ||
CNHFAHCC_06868 | 7.5e-200 | gerBB | E | Spore germination protein | ||
CNHFAHCC_06869 | 7.6e-216 | gerAC | S | Spore germination protein | ||
CNHFAHCC_06870 | 1.9e-248 | ywtG | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06871 | 8.4e-171 | ywtF | K | Transcriptional regulator | ||
CNHFAHCC_06872 | 7e-161 | ywtE | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
CNHFAHCC_06873 | 5e-240 | pgdS | CBM50 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
CNHFAHCC_06874 | 3.6e-21 | ywtC | ||||
CNHFAHCC_06875 | 1.7e-218 | capA | M | enzyme of poly-gamma-glutamate biosynthesis (capsule formation) | ||
CNHFAHCC_06876 | 8.6e-70 | pgsC | S | biosynthesis protein | ||
CNHFAHCC_06877 | 6.1e-224 | murD | 6.3.2.9 | M | COG0769 UDP-N-acetylmuramyl tripeptide synthase | |
CNHFAHCC_06878 | 1.5e-180 | rbsR | K | transcriptional | ||
CNHFAHCC_06879 | 2.9e-162 | rbsK | 2.7.1.15, 2.7.1.4 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
CNHFAHCC_06880 | 2.8e-64 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
CNHFAHCC_06881 | 2.3e-276 | rbsA | 3.6.3.17 | G | Part of the ABC transporter complex RbsABC involved in ribose import. Responsible for energy coupling to the transport system | |
CNHFAHCC_06882 | 1.4e-154 | rbsC | G | Belongs to the binding-protein-dependent transport system permease family | ||
CNHFAHCC_06883 | 4.4e-161 | rbsB | G | COG1879 ABC-type sugar transport system, periplasmic component | ||
CNHFAHCC_06884 | 4.6e-94 | batE | T | Sh3 type 3 domain protein | ||
CNHFAHCC_06885 | 3.6e-48 | ywsA | S | Protein of unknown function (DUF3892) | ||
CNHFAHCC_06886 | 1.5e-97 | ywrO | S | NADPH-quinone reductase (modulator of drug activity B) | ||
CNHFAHCC_06887 | 1.3e-145 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
CNHFAHCC_06888 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
CNHFAHCC_06889 | 1.1e-169 | alsR | K | LysR substrate binding domain | ||
CNHFAHCC_06890 | 3.3e-239 | ywrK | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
CNHFAHCC_06891 | 7.5e-126 | ywrJ | ||||
CNHFAHCC_06892 | 7.6e-131 | cotB | ||||
CNHFAHCC_06893 | 1.2e-210 | cotH | M | Spore Coat | ||
CNHFAHCC_06894 | 3.7e-12 | |||||
CNHFAHCC_06895 | 8.1e-111 | ywrF | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | ||
CNHFAHCC_06896 | 2.9e-54 | S | Domain of unknown function (DUF4181) | |||
CNHFAHCC_06897 | 9.6e-310 | ggt | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
CNHFAHCC_06898 | 2.9e-82 | ywrC | K | Transcriptional regulator | ||
CNHFAHCC_06899 | 2.4e-104 | ywrB | P | Chromate transporter | ||
CNHFAHCC_06900 | 6.9e-90 | ywrA | P | COG2059 Chromate transport protein ChrA | ||
CNHFAHCC_06902 | 2.7e-102 | ywqN | S | NAD(P)H-dependent | ||
CNHFAHCC_06903 | 2.9e-162 | K | Transcriptional regulator | |||
CNHFAHCC_06904 | 4.5e-137 | nfi | 3.1.21.7 | L | DNA repair enzyme involved in the repair of deaminated bases. Selectively cleaves double-stranded DNA at the second phosphodiester bond 3' to a deoxyinosine leaving behind the intact lesion on the nicked DNA | |
CNHFAHCC_06905 | 1.7e-52 | S | MORN repeat variant | |||
CNHFAHCC_06906 | 0.0 | ywqJ | L | nucleic acid phosphodiester bond hydrolysis | ||
CNHFAHCC_06907 | 1.3e-38 | ywqI | S | Family of unknown function (DUF5344) | ||
CNHFAHCC_06908 | 3.3e-15 | S | Domain of unknown function (DUF5082) | |||
CNHFAHCC_06909 | 3.4e-154 | ywqG | S | Domain of unknown function (DUF1963) | ||
CNHFAHCC_06910 | 3e-248 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
CNHFAHCC_06911 | 1.4e-141 | ywqE | 3.1.3.48 | GM | COG4464 Capsular polysaccharide biosynthesis protein | |
CNHFAHCC_06912 | 1.1e-119 | ywqD | 2.7.10.1 | D | COG0489 ATPases involved in chromosome partitioning | |
CNHFAHCC_06913 | 2e-116 | ywqC | M | biosynthesis protein | ||
CNHFAHCC_06914 | 1.2e-17 | |||||
CNHFAHCC_06915 | 3.8e-309 | ywqB | S | SWIM zinc finger | ||
CNHFAHCC_06916 | 0.0 | ywqA | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
CNHFAHCC_06917 | 3.6e-157 | ywpJ | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
CNHFAHCC_06918 | 9.2e-139 | glcR | K | COG1349 Transcriptional regulators of sugar metabolism | ||
CNHFAHCC_06919 | 9.8e-58 | ssbB | L | Single-stranded DNA-binding protein | ||
CNHFAHCC_06920 | 1.3e-66 | ywpG | ||||
CNHFAHCC_06921 | 1.1e-66 | ywpF | S | YwpF-like protein | ||
CNHFAHCC_06922 | 8e-51 | srtA | 3.4.22.70 | M | Sortase family | |
CNHFAHCC_06923 | 1.4e-153 | ywpD | T | Histidine kinase | ||
CNHFAHCC_06924 | 1.5e-54 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
CNHFAHCC_06925 | 4.6e-82 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
CNHFAHCC_06926 | 2.1e-199 | S | aspartate phosphatase | |||
CNHFAHCC_06927 | 1.5e-141 | flhP | N | flagellar basal body | ||
CNHFAHCC_06928 | 5.4e-126 | flhO | N | flagellar basal body | ||
CNHFAHCC_06929 | 3.5e-180 | mbl | D | Rod shape-determining protein | ||
CNHFAHCC_06930 | 3e-44 | spoIIID | K | Stage III sporulation protein D | ||
CNHFAHCC_06931 | 2.1e-70 | ywoH | K | COG1846 Transcriptional regulators | ||
CNHFAHCC_06932 | 4.4e-203 | ywoG | EGP | Major facilitator Superfamily | ||
CNHFAHCC_06933 | 9.7e-232 | ywoF | P | Right handed beta helix region | ||
CNHFAHCC_06934 | 3e-281 | ybbW | FH | COG1953 Cytosine uracil thiamine allantoin permeases | ||
CNHFAHCC_06935 | 4.4e-242 | ywoD | EGP | Major facilitator superfamily | ||
CNHFAHCC_06936 | 4e-104 | phzA | Q | Isochorismatase family | ||
CNHFAHCC_06937 | 1.2e-77 | |||||
CNHFAHCC_06938 | 2.5e-225 | amt | P | Ammonium transporter | ||
CNHFAHCC_06939 | 1.6e-58 | nrgB | K | Belongs to the P(II) protein family | ||
CNHFAHCC_06940 | 3.4e-103 | bcrC | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | |
CNHFAHCC_06941 | 3.5e-73 | ywnJ | S | VanZ like family | ||
CNHFAHCC_06942 | 5.5e-126 | spoIIQ | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
CNHFAHCC_06943 | 6.4e-90 | ywnH | 2.3.1.183 | M | COG1247 Sortase and related acyltransferases | |
CNHFAHCC_06944 | 2.7e-14 | ywnC | S | Family of unknown function (DUF5362) | ||
CNHFAHCC_06945 | 2.2e-70 | ywnF | S | Family of unknown function (DUF5392) | ||
CNHFAHCC_06946 | 1.2e-277 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
CNHFAHCC_06947 | 4.1e-144 | mta | K | transcriptional | ||
CNHFAHCC_06948 | 2.6e-59 | ywnC | S | Family of unknown function (DUF5362) | ||
CNHFAHCC_06949 | 1.6e-114 | ywnB | S | NAD(P)H-binding | ||
CNHFAHCC_06950 | 1.7e-64 | ywnA | K | Transcriptional regulator | ||
CNHFAHCC_06951 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
CNHFAHCC_06952 | 5.9e-64 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
CNHFAHCC_06953 | 6.3e-51 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
CNHFAHCC_06955 | 3.8e-11 | csbD | K | CsbD-like | ||
CNHFAHCC_06956 | 3e-84 | ywmF | S | Peptidase M50 | ||
CNHFAHCC_06957 | 1.3e-103 | S | response regulator aspartate phosphatase | |||
CNHFAHCC_06958 | 7e-192 | moaA | 4.1.99.22, 4.6.1.17 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
CNHFAHCC_06959 | 2.6e-146 | fdhD | C | Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH | ||
CNHFAHCC_06961 | 7.2e-121 | ywmD | S | protein containing a von Willebrand factor type A (vWA) domain | ||
CNHFAHCC_06962 | 1.7e-122 | ywmC | S | protein containing a von Willebrand factor type A (vWA) domain | ||
CNHFAHCC_06963 | 2e-178 | spoIID | D | Stage II sporulation protein D | ||
CNHFAHCC_06964 | 1.2e-241 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
CNHFAHCC_06965 | 1.6e-134 | ywmB | S | TATA-box binding | ||
CNHFAHCC_06966 | 1.3e-32 | ywzB | S | membrane | ||
CNHFAHCC_06967 | 4.3e-88 | ywmA | ||||
CNHFAHCC_06968 | 5.9e-54 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
CNHFAHCC_06969 | 1.2e-266 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
CNHFAHCC_06970 | 1.1e-150 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
CNHFAHCC_06971 | 6.9e-281 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
CNHFAHCC_06972 | 1.1e-90 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
CNHFAHCC_06973 | 3.8e-45 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
CNHFAHCC_06974 | 1.6e-26 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
CNHFAHCC_06975 | 4.6e-129 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
CNHFAHCC_06976 | 2.5e-62 | atpI | S | ATP synthase | ||
CNHFAHCC_06977 | 4.7e-114 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
CNHFAHCC_06978 | 2.1e-238 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
CNHFAHCC_06979 | 7.2e-95 | ywlG | S | Belongs to the UPF0340 family | ||
CNHFAHCC_06980 | 1.7e-81 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
CNHFAHCC_06981 | 1.7e-78 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
CNHFAHCC_06982 | 1.7e-91 | mntP | P | Probably functions as a manganese efflux pump | ||
CNHFAHCC_06983 | 1.2e-196 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
CNHFAHCC_06984 | 1.3e-76 | ywlB | 1.20.4.1, 2.3.1.1 | E | Belongs to the acetyltransferase family. ArgA subfamily | |
CNHFAHCC_06985 | 6.1e-112 | spoIIR | S | stage II sporulation protein R | ||
CNHFAHCC_06986 | 3.4e-56 | ywlA | S | Uncharacterised protein family (UPF0715) | ||
CNHFAHCC_06988 | 2.3e-159 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
CNHFAHCC_06989 | 9.5e-192 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
CNHFAHCC_06990 | 8.2e-69 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
CNHFAHCC_06991 | 1.7e-91 | racA | K | Required for the formation of axial filaments and for anchoring the origin regions at the cell poles in sporulating cells, thus ensuring proper chromosome segregation in the prespore. Binds in a dispersed manner throughout the chromosome but preferentially to sites clustered in the origin portion of the chromosome, causing condensation of the chromosome and its remodeling into an elongated, anchored structure | ||
CNHFAHCC_06992 | 8.6e-160 | ywkB | S | Membrane transport protein | ||
CNHFAHCC_06993 | 0.0 | sfcA | 1.1.1.38 | C | malic enzyme | |
CNHFAHCC_06995 | 2.4e-104 | tdk | 2.7.1.21 | F | thymidine kinase | |
CNHFAHCC_06996 | 1.1e-32 | rpmE | J | Binds the 23S rRNA | ||
CNHFAHCC_06997 | 2.8e-238 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
CNHFAHCC_06998 | 1.9e-175 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
CNHFAHCC_06999 | 8.6e-240 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
CNHFAHCC_07000 | 1.5e-112 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
CNHFAHCC_07001 | 7.2e-158 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
CNHFAHCC_07002 | 1.1e-62 | spo0F | T | COG0784 FOG CheY-like receiver | ||
CNHFAHCC_07003 | 2.4e-92 | ywjG | S | Domain of unknown function (DUF2529) | ||
CNHFAHCC_07004 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
CNHFAHCC_07005 | 1.5e-49 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
CNHFAHCC_07006 | 2.6e-211 | acdA | 1.3.8.1, 1.3.8.7 | I | acyl-CoA dehydrogenase | |
CNHFAHCC_07007 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
CNHFAHCC_07008 | 2.3e-223 | clsB | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
CNHFAHCC_07009 | 6.6e-184 | uvsE | L | Component in a DNA repair pathway. Removal of UV-light damaged nucleotides. Recognizes pyrimidine dimers and cleave a phosphodiester bond immediately 5' to the lesion | ||
CNHFAHCC_07010 | 2.7e-42 | ywjC | ||||
CNHFAHCC_07011 | 4.8e-96 | ywjB | H | RibD C-terminal domain | ||
CNHFAHCC_07012 | 6.8e-311 | ywjA | V | ABC transporter | ||
CNHFAHCC_07013 | 6.4e-287 | ywiE | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
CNHFAHCC_07014 | 1.8e-124 | narI | 1.7.5.1 | C | nitrate reductase, gamma | |
CNHFAHCC_07015 | 2.4e-98 | narJ | 1.7.5.1 | C | nitrate reductase | |
CNHFAHCC_07016 | 1e-297 | narH | 1.7.5.1 | C | Nitrate reductase, beta | |
CNHFAHCC_07017 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
CNHFAHCC_07018 | 7e-86 | arfM | T | cyclic nucleotide binding | ||
CNHFAHCC_07019 | 4.3e-140 | ywiC | S | YwiC-like protein | ||
CNHFAHCC_07020 | 5.3e-130 | fnr | K | helix_turn_helix, cAMP Regulatory protein | ||
CNHFAHCC_07021 | 1e-213 | narK | P | COG2223 Nitrate nitrite transporter | ||
CNHFAHCC_07022 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
CNHFAHCC_07023 | 4.7e-73 | ywiB | S | protein conserved in bacteria | ||
CNHFAHCC_07024 | 1e-07 | S | Bacteriocin subtilosin A | |||
CNHFAHCC_07025 | 7e-269 | C | Fe-S oxidoreductases | |||
CNHFAHCC_07026 | 3.3e-132 | cbiO | V | ABC transporter | ||
CNHFAHCC_07027 | 3.1e-237 | mgtA | 3.6.3.2 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
CNHFAHCC_07028 | 3.5e-219 | 2.7.1.26, 2.7.7.2 | L | Peptidase, M16 | ||
CNHFAHCC_07029 | 1.2e-249 | L | Peptidase, M16 | |||
CNHFAHCC_07031 | 2.9e-249 | ywhL | CO | amine dehydrogenase activity | ||
CNHFAHCC_07032 | 2.5e-205 | ywhK | CO | amine dehydrogenase activity | ||
CNHFAHCC_07033 | 2.3e-79 | S | aspartate phosphatase | |||
CNHFAHCC_07035 | 1e-84 | ywhH | S | Aminoacyl-tRNA editing domain | ||
CNHFAHCC_07036 | 9.2e-169 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
CNHFAHCC_07037 | 1.4e-158 | speE | 2.5.1.16 | E | Catalyzes the irreversible transfer of a propylamine group from the amino donor S-adenosylmethioninamine (decarboxy- AdoMet) to putrescine (1,4-diaminobutane) to yield spermidine | |
CNHFAHCC_07038 | 0.0 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
CNHFAHCC_07039 | 5.2e-95 | ywhD | S | YwhD family | ||
CNHFAHCC_07040 | 5.1e-119 | ywhC | S | Peptidase family M50 | ||
CNHFAHCC_07041 | 2.7e-25 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
CNHFAHCC_07042 | 3.5e-71 | ywhA | K | Transcriptional regulator | ||
CNHFAHCC_07043 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
CNHFAHCC_07045 | 2.6e-242 | mmr | U | Major Facilitator Superfamily | ||
CNHFAHCC_07046 | 2.8e-79 | yffB | K | Transcriptional regulator | ||
CNHFAHCC_07047 | 5.4e-89 | ywgA | 2.1.1.72, 3.1.21.3 | |||
CNHFAHCC_07048 | 1.8e-256 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
CNHFAHCC_07049 | 3.1e-36 | ywzC | S | Belongs to the UPF0741 family | ||
CNHFAHCC_07050 | 1.6e-111 | rsfA_1 | ||||
CNHFAHCC_07051 | 5.2e-159 | ywfM | EG | EamA-like transporter family | ||
CNHFAHCC_07052 | 6.6e-156 | lipL | 2.3.1.200, 2.3.1.204 | H | Catalyzes the amidotransfer (transamidation) of the octanoyl moiety from octanoyl-GcvH to the lipoyl domain of the E2 subunit of lipoate-dependent enzymes | |
CNHFAHCC_07053 | 7.2e-164 | cysL | K | Transcriptional regulator | ||
CNHFAHCC_07054 | 6.6e-176 | pta | 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
CNHFAHCC_07055 | 1.1e-146 | ywfI | C | May function as heme-dependent peroxidase | ||
CNHFAHCC_07056 | 3.4e-135 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_07057 | 2.7e-235 | ywfG | 2.6.1.83 | E | Aminotransferase class I and II | |
CNHFAHCC_07058 | 2.9e-210 | bacE | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07059 | 3.6e-271 | purD | 6.3.2.49, 6.3.4.13 | F | Part of the bacABCDEFG operon responsible for the biosynthesis of bacilysin, an irreversible inactivator of the glutaminase domain of glucosamine synthetase. Catalyzes the formation of alpha-dipeptides from various L-amino acids in the presence of ATP. In vivo catalyzes the ligation of L-alanine and L-anticapsin (epoxycyclohexanonyl-Ala) to produce the final bacilysin antibiotic (L-Ala-L-4S-cyclohexenonyl-Ala dipeptide) | |
CNHFAHCC_07060 | 1.3e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
CNHFAHCC_07061 | 1.3e-136 | bacB | 5.3.3.19, 5.4.99.5 | S | Part of the bacABCDEF operon responsible for the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. Bacilysin is an irreversible inactivator of the glutaminase domain of glucosamine synthetase. BacB catalyzes the allylic isomerization of the | |
CNHFAHCC_07062 | 3.3e-112 | pheA | 1.1.1.3, 1.3.1.12, 4.1.1.100, 4.2.1.51, 5.4.99.5 | E | Part of the bacABCDEF operon responsible for the biosynthesis of the nonribosomally synthesized dipeptide antibiotic bacilysin, composed of L-alanine and L-anticapsin. Bacilysin is an irreversible inactivator of the glutaminase domain of glucosamine synthetase. BacA is an unusual prephenate decarboxylase that avoids the typical aromatization of the cyclohexadienol ring of prephenate. BacA catalyzes the protonation of prephenate (1-carboxy-4-hydroxy-alpha-oxo-2,5-cyclohexadiene-1- propanoic acid) at C6 position, followed by a decarboxylation to produce the endocyclic-delta(4),delta(8)-7R-dihydro- hydroxyphenylpyruvate (en-H2HPP). En-H2HPP is able to undergo a slow nonenzymatic isomerization to produce the exocyclic- delta(3),delta(5)-dihydro-hydroxyphenylpyruvate (ex-H2HPP). BacA isomerizes only the pro-R double bond in prephenate | |
CNHFAHCC_07063 | 4.6e-206 | ywfA | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07064 | 4e-262 | lysP | E | amino acid | ||
CNHFAHCC_07065 | 0.0 | rocB | E | arginine degradation protein | ||
CNHFAHCC_07066 | 1.4e-297 | putA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
CNHFAHCC_07067 | 7.5e-244 | rocG | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
CNHFAHCC_07068 | 1.8e-78 | |||||
CNHFAHCC_07069 | 3.5e-87 | spsL | 5.1.3.13 | M | Spore Coat | |
CNHFAHCC_07070 | 5.3e-161 | spsK | 1.1.1.133 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
CNHFAHCC_07071 | 1e-181 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
CNHFAHCC_07072 | 1.9e-138 | spsI | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
CNHFAHCC_07073 | 1.7e-190 | spsG | M | Spore Coat | ||
CNHFAHCC_07074 | 9.7e-132 | spsF | M | Spore Coat | ||
CNHFAHCC_07075 | 3.2e-214 | spsE | 2.5.1.56 | M | acid synthase | |
CNHFAHCC_07076 | 4e-164 | spsD | 2.3.1.210 | K | Spore Coat | |
CNHFAHCC_07077 | 1.6e-224 | spsC | E | Belongs to the DegT DnrJ EryC1 family | ||
CNHFAHCC_07078 | 1.8e-278 | spsB | M | Capsule polysaccharide biosynthesis protein | ||
CNHFAHCC_07079 | 2.8e-145 | spsA | M | Spore Coat | ||
CNHFAHCC_07080 | 4.8e-75 | gerQ | S | Essential for the localization of CwlJ in the spore coat and for spore germination triggered by calcium and dipicolinic acid (DPA). Its assembly into the spore coat is dependent on the coat morphogenetic proteins CotE and SpoIVA | ||
CNHFAHCC_07081 | 4.3e-59 | ywdK | S | small membrane protein | ||
CNHFAHCC_07082 | 1.3e-238 | ywdJ | F | Xanthine uracil | ||
CNHFAHCC_07083 | 7.7e-49 | ywdI | S | Family of unknown function (DUF5327) | ||
CNHFAHCC_07084 | 5.9e-263 | ywdH | 1.2.1.3 | C | Belongs to the aldehyde dehydrogenase family | |
CNHFAHCC_07085 | 5e-130 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
CNHFAHCC_07086 | 1.1e-152 | ywdF | GT2,GT4 | S | Glycosyltransferase like family 2 | |
CNHFAHCC_07088 | 1.4e-113 | ywdD | ||||
CNHFAHCC_07089 | 1.3e-57 | pex | K | Transcriptional regulator PadR-like family | ||
CNHFAHCC_07090 | 9.3e-147 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
CNHFAHCC_07091 | 2e-28 | ywdA | ||||
CNHFAHCC_07092 | 9.5e-296 | scrB | 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH32 | G | invertase |
CNHFAHCC_07093 | 3.9e-254 | scrA | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_07094 | 1e-139 | focA | P | Formate/nitrite transporter | ||
CNHFAHCC_07095 | 2.4e-150 | sacT | K | transcriptional antiterminator | ||
CNHFAHCC_07097 | 0.0 | vpr | O | Belongs to the peptidase S8 family | ||
CNHFAHCC_07098 | 5.1e-187 | ywcH | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_07099 | 7.2e-138 | nfrA | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
CNHFAHCC_07100 | 2.9e-202 | rodA | D | Belongs to the SEDS family | ||
CNHFAHCC_07101 | 2.7e-39 | ywcE | S | Required for proper spore morphogenesis. Important for spore germination | ||
CNHFAHCC_07102 | 2.6e-64 | qoxD | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
CNHFAHCC_07103 | 1.2e-111 | qoxC | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
CNHFAHCC_07104 | 0.0 | qoxB | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
CNHFAHCC_07105 | 2.1e-177 | cyoA | 1.10.3.10, 1.10.3.12 | C | Catalyzes quinol oxidation with the concomitant reduction of oxygen to water. Subunit II transfers the electrons from a quinol to the binuclear center of the catalytic subunit I | |
CNHFAHCC_07106 | 1e-35 | ywzA | S | membrane | ||
CNHFAHCC_07107 | 3.7e-306 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
CNHFAHCC_07108 | 6.2e-229 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
CNHFAHCC_07109 | 9.5e-60 | gtcA | S | GtrA-like protein | ||
CNHFAHCC_07110 | 2.2e-122 | ywcC | K | transcriptional regulator | ||
CNHFAHCC_07112 | 9.8e-49 | ywcB | S | Protein of unknown function, DUF485 | ||
CNHFAHCC_07113 | 1.4e-268 | ywcA | S | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
CNHFAHCC_07114 | 1.9e-112 | ywbO | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
CNHFAHCC_07115 | 2.6e-225 | ywbN | P | Dyp-type peroxidase family protein | ||
CNHFAHCC_07116 | 2e-187 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
CNHFAHCC_07117 | 8.2e-255 | P | COG0672 High-affinity Fe2 Pb2 permease | |||
CNHFAHCC_07118 | 4.1e-116 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
CNHFAHCC_07119 | 2.8e-143 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
CNHFAHCC_07120 | 4.3e-153 | ywbI | K | Transcriptional regulator | ||
CNHFAHCC_07121 | 6.5e-58 | ywbH | S | Increases the activity of extracellular murein hydrolases possibly by mediating their export via hole formation. Inhibited by the antiholin-like proteins LrgAB. In an unstressed cell, the LrgAB products probably inhibit the function of the CidA protein. When a cell is stressed by the addition of antibiotics or by other factors in the environment, CidA possibly oligomerizes within the bacterial cell membrane, creating lesions that disrupt the proton motive force, which in turn results in loss of cell viability. These lesions are also hypothesized to regulate the subsequent cell lysis by either allowing the murein hydrolases access to the cell wall substrate and or regulating their activity by a | ||
CNHFAHCC_07122 | 2.3e-111 | ywbG | M | effector of murein hydrolase | ||
CNHFAHCC_07123 | 1.9e-209 | ywbF | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07124 | 1.2e-28 | ywbE | S | Uncharacterized conserved protein (DUF2196) | ||
CNHFAHCC_07125 | 8.9e-223 | ywbD | 2.1.1.191 | J | Methyltransferase | |
CNHFAHCC_07126 | 4.4e-67 | ywbC | 4.4.1.5 | E | glyoxalase | |
CNHFAHCC_07127 | 1.8e-127 | ywbB | S | Protein of unknown function (DUF2711) | ||
CNHFAHCC_07128 | 5.8e-247 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CNHFAHCC_07129 | 1.6e-277 | epr | 3.4.21.62 | O | Belongs to the peptidase S8 family | |
CNHFAHCC_07130 | 5.2e-243 | scrA | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_07131 | 4e-153 | sacY | K | transcriptional antiterminator | ||
CNHFAHCC_07132 | 7e-169 | gspA | M | General stress | ||
CNHFAHCC_07133 | 1.7e-128 | ywaF | S | Integral membrane protein | ||
CNHFAHCC_07134 | 8.1e-88 | ywaE | K | Transcriptional regulator | ||
CNHFAHCC_07135 | 4.4e-233 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
CNHFAHCC_07136 | 1.4e-251 | ywaD | 3.4.11.10, 3.4.11.6 | S | PA domain | |
CNHFAHCC_07137 | 5e-116 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
CNHFAHCC_07138 | 5.4e-167 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
CNHFAHCC_07140 | 5e-14 | S | D-Ala-teichoic acid biosynthesis protein | |||
CNHFAHCC_07141 | 7.9e-293 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
CNHFAHCC_07142 | 1.2e-232 | dltB | M | membrane protein involved in D-alanine export | ||
CNHFAHCC_07143 | 1.5e-36 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
CNHFAHCC_07144 | 2.3e-231 | dltD | M | COG3966 Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
CNHFAHCC_07145 | 6.6e-139 | dltE | M | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
CNHFAHCC_07146 | 3.1e-206 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
CNHFAHCC_07147 | 1.1e-253 | licH | 3.2.1.86 | GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
CNHFAHCC_07148 | 6.7e-38 | licA | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
CNHFAHCC_07149 | 7.4e-250 | licC | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
CNHFAHCC_07150 | 2.3e-50 | licB | 2.7.1.196, 2.7.1.205 | G | transporter subunit IIB | |
CNHFAHCC_07151 | 0.0 | licR | 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
CNHFAHCC_07152 | 1.1e-19 | yxzF | ||||
CNHFAHCC_07153 | 1e-110 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
CNHFAHCC_07154 | 0.0 | katX | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
CNHFAHCC_07155 | 2.1e-216 | yxlH | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07156 | 1.8e-139 | yxlG | S | COG1277 ABC-type transport system involved in multi-copper enzyme maturation, permease component | ||
CNHFAHCC_07157 | 5.1e-167 | yxlF | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_07158 | 7.6e-28 | yxlE | S | Phospholipase_D-nuclease N-terminal | ||
CNHFAHCC_07159 | 1.2e-31 | |||||
CNHFAHCC_07160 | 3.9e-48 | yxlC | S | Family of unknown function (DUF5345) | ||
CNHFAHCC_07161 | 4.7e-91 | sigY | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
CNHFAHCC_07162 | 2.3e-254 | yxlA | F | Belongs to the purine-cytosine permease (2.A.39) family | ||
CNHFAHCC_07163 | 8e-162 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
CNHFAHCC_07164 | 0.0 | cydD | V | ATP-binding protein | ||
CNHFAHCC_07165 | 0.0 | cydD | V | ATP-binding | ||
CNHFAHCC_07166 | 2.9e-190 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase, subunit II | |
CNHFAHCC_07167 | 1.3e-268 | cydA | 1.10.3.14 | C | oxidase, subunit | |
CNHFAHCC_07168 | 1.5e-229 | cimH | C | COG3493 Na citrate symporter | ||
CNHFAHCC_07169 | 0.0 | 3.4.24.84 | O | Peptidase family M48 | ||
CNHFAHCC_07170 | 3e-156 | yxkH | G | Polysaccharide deacetylase | ||
CNHFAHCC_07171 | 5.9e-205 | msmK | P | Belongs to the ABC transporter superfamily | ||
CNHFAHCC_07172 | 4.8e-165 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
CNHFAHCC_07173 | 2.5e-275 | aldY | 1.2.1.3 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
CNHFAHCC_07174 | 1.9e-147 | yxkD | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
CNHFAHCC_07175 | 4.1e-73 | yxkC | S | Domain of unknown function (DUF4352) | ||
CNHFAHCC_07176 | 4.6e-196 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
CNHFAHCC_07177 | 1.3e-95 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
CNHFAHCC_07178 | 1.9e-166 | yxjO | K | LysR substrate binding domain | ||
CNHFAHCC_07179 | 2.4e-78 | S | Protein of unknown function (DUF1453) | |||
CNHFAHCC_07180 | 1.5e-193 | yxjM | T | Signal transduction histidine kinase | ||
CNHFAHCC_07181 | 8.9e-116 | K | helix_turn_helix, Lux Regulon | |||
CNHFAHCC_07182 | 3.6e-235 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
CNHFAHCC_07185 | 1e-87 | yxjI | S | LURP-one-related | ||
CNHFAHCC_07186 | 5.5e-222 | yxjG | 2.1.1.14 | E | Methionine synthase | |
CNHFAHCC_07187 | 1e-220 | yxjG | 2.1.1.14 | E | Methionine synthase | |
CNHFAHCC_07188 | 1.3e-137 | IQ | Catalyzes the formation of acetoacetate from 3-hydroxybutyrate | |||
CNHFAHCC_07189 | 6.8e-113 | scoB | 2.8.3.5 | I | COG2057 Acyl CoA acetate 3-ketoacid CoA transferase, beta subunit | |
CNHFAHCC_07190 | 1.4e-130 | scoA | 2.8.3.5 | I | COG1788 Acyl CoA acetate 3-ketoacid CoA transferase, alpha subunit | |
CNHFAHCC_07191 | 2.6e-253 | yxjC | EG | COG2610 H gluconate symporter and related permeases | ||
CNHFAHCC_07192 | 3.2e-161 | rlmA | 2.1.1.187 | Q | Methyltransferase domain | |
CNHFAHCC_07193 | 1.9e-212 | nupG | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
CNHFAHCC_07194 | 5e-35 | T | Domain of unknown function (DUF4163) | |||
CNHFAHCC_07195 | 1.2e-22 | T | Domain of unknown function (DUF4163) | |||
CNHFAHCC_07196 | 2.7e-48 | yxiS | ||||
CNHFAHCC_07197 | 0.0 | katE | 1.11.1.6, 3.5.1.124 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
CNHFAHCC_07198 | 6.6e-224 | citH | C | Citrate transporter | ||
CNHFAHCC_07199 | 5e-144 | exoK | GH16 | M | licheninase activity | |
CNHFAHCC_07200 | 8.3e-151 | licT | K | transcriptional antiterminator | ||
CNHFAHCC_07201 | 6.6e-114 | |||||
CNHFAHCC_07202 | 3.2e-224 | yxiO | S | COG2270 Permeases of the major facilitator superfamily | ||
CNHFAHCC_07203 | 1e-265 | dbpA | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in the assembly of the 50S ribosomal subunit. Has an RNA-dependent ATPase activity, which is specific for 23S rRNA, and a 3' to 5' RNA helicase activity that uses the energy of ATP hydrolysis to destabilize and unwind short rRNA duplexes | |
CNHFAHCC_07204 | 7.5e-219 | 3.2.1.14 | GH18 | E | GDSL-like Lipase/Acylhydrolase | |
CNHFAHCC_07206 | 1.6e-48 | yxiJ | S | YxiJ-like protein | ||
CNHFAHCC_07207 | 1.2e-96 | yxiI | S | Protein of unknown function (DUF2716) | ||
CNHFAHCC_07208 | 3.8e-81 | |||||
CNHFAHCC_07209 | 4.9e-46 | |||||
CNHFAHCC_07210 | 3.7e-75 | yxiG | ||||
CNHFAHCC_07211 | 6.4e-63 | |||||
CNHFAHCC_07212 | 1.7e-84 | |||||
CNHFAHCC_07213 | 1.5e-71 | yxxG | ||||
CNHFAHCC_07214 | 0.0 | wapA | M | COG3209 Rhs family protein | ||
CNHFAHCC_07215 | 2.9e-168 | yxxF | EG | EamA-like transporter family | ||
CNHFAHCC_07216 | 1.1e-72 | yxiE | T | Belongs to the universal stress protein A family | ||
CNHFAHCC_07217 | 6.5e-281 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CNHFAHCC_07218 | 0.0 | bglF | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
CNHFAHCC_07219 | 3.6e-51 | |||||
CNHFAHCC_07220 | 2.2e-78 | S | SMI1 / KNR4 family | |||
CNHFAHCC_07221 | 0.0 | S | nuclease activity | |||
CNHFAHCC_07222 | 3.6e-39 | yxiC | S | Family of unknown function (DUF5344) | ||
CNHFAHCC_07223 | 2.1e-21 | S | Domain of unknown function (DUF5082) | |||
CNHFAHCC_07224 | 6.3e-284 | yxiA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
CNHFAHCC_07226 | 5e-78 | hutP | K | Antiterminator that binds to cis-acting regulatory sequences on the mRNA in the presence of histidine, thereby suppressing transcription termination and activating the hut operon for histidine utilization | ||
CNHFAHCC_07227 | 2.3e-284 | hutH | 4.3.1.3 | E | Histidine ammonia-lyase | |
CNHFAHCC_07228 | 0.0 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
CNHFAHCC_07229 | 1.2e-238 | hutI | 3.5.2.7 | Q | Imidazolone-5-propionate hydrolase | |
CNHFAHCC_07230 | 8e-182 | hutG | 3.5.3.11, 3.5.3.8 | E | Catalyzes the conversion of N-formimidoyl-L-glutamate to L-glutamate and formamide | |
CNHFAHCC_07231 | 6.1e-252 | lysP | E | amino acid | ||
CNHFAHCC_07232 | 4.2e-234 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase | |
CNHFAHCC_07233 | 9.8e-206 | nupC | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
CNHFAHCC_07234 | 7e-116 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
CNHFAHCC_07235 | 3.5e-174 | deoR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
CNHFAHCC_07236 | 3e-153 | yxxB | S | Domain of Unknown Function (DUF1206) | ||
CNHFAHCC_07237 | 6.8e-201 | eutH | E | Ethanolamine utilisation protein, EutH | ||
CNHFAHCC_07238 | 2e-255 | yxeQ | S | MmgE/PrpD family | ||
CNHFAHCC_07239 | 3.8e-215 | yxeP | 3.5.1.47 | E | hydrolase activity | |
CNHFAHCC_07240 | 5.4e-133 | yxeO | 3.6.3.21 | P | ABC transporter, ATP-binding protein | |
CNHFAHCC_07241 | 5.4e-108 | yxeN | P | COG0765 ABC-type amino acid transport system, permease component | ||
CNHFAHCC_07242 | 2.5e-144 | yxeM | M | Belongs to the bacterial solute-binding protein 3 family | ||
CNHFAHCC_07243 | 7.3e-94 | yxeL | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
CNHFAHCC_07244 | 2.2e-254 | yxeK | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
CNHFAHCC_07246 | 8.8e-192 | yxeI | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
CNHFAHCC_07247 | 6.2e-151 | yidA | S | hydrolases of the HAD superfamily | ||
CNHFAHCC_07250 | 1.3e-20 | yxeE | ||||
CNHFAHCC_07251 | 1.9e-16 | yxeD | ||||
CNHFAHCC_07252 | 8.5e-69 | |||||
CNHFAHCC_07253 | 6e-177 | fhuD | P | ABC transporter | ||
CNHFAHCC_07254 | 1.5e-58 | yxeA | S | Protein of unknown function (DUF1093) | ||
CNHFAHCC_07255 | 0.0 | yxdM | V | ABC transporter (permease) | ||
CNHFAHCC_07256 | 9.4e-141 | yxdL | V | ABC transporter, ATP-binding protein | ||
CNHFAHCC_07257 | 1.3e-182 | T | PhoQ Sensor | |||
CNHFAHCC_07258 | 2.9e-122 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_07259 | 5.4e-161 | iolJ | 4.1.2.13, 4.1.2.29 | F | Produces dihydroxyacetone phosphate (DHAP or glycerone phosphate) and malonic semialdehyde (MSA or 3-oxopropanoate) from 6-phospho-5-dehydro-2-deoxy-D-gluconate (DKGP) | |
CNHFAHCC_07260 | 1.9e-139 | iolI | 5.3.99.11 | G | Involved in the reversible interconverion of 2-keto-myo- inositol (2KMI, inosose or 2,4,6 3,5-pentahydroxycyclohexanone) to 1-keto-D-chiro-inositol (1KDCI or 2,3,5 4,6- pentahydroxycyclohexanone) | |
CNHFAHCC_07261 | 2.3e-167 | iolH | G | Xylose isomerase-like TIM barrel | ||
CNHFAHCC_07262 | 2.8e-196 | iolG | 1.1.1.18, 1.1.1.369 | S | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
CNHFAHCC_07263 | 1.3e-235 | iolF | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07264 | 2.1e-176 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
CNHFAHCC_07265 | 0.0 | iolD | 3.7.1.22 | E | Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) | |
CNHFAHCC_07266 | 2.9e-179 | iolC | 2.7.1.92 | G | Catalyzes the phosphorylation of 5-dehydro-2-deoxy-D- gluconate (2-deoxy-5-keto-D-gluconate or DKG) to 6-phospho-5- dehydro-2-deoxy-D-gluconate (DKGP) | |
CNHFAHCC_07267 | 1.1e-155 | iolB | 5.3.1.30 | G | Involved in the isomerization of 5-deoxy-glucuronate (5DG) to 5-dehydro-2-deoxy-D-gluconate (DKG or 2-deoxy-5-keto-D- gluconate) | |
CNHFAHCC_07268 | 1.4e-281 | iolA | 1.2.1.18, 1.2.1.27 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
CNHFAHCC_07269 | 3.3e-138 | iolR | K | COG1349 Transcriptional regulators of sugar metabolism | ||
CNHFAHCC_07270 | 3.7e-176 | iolS | C | Aldo keto reductase | ||
CNHFAHCC_07272 | 8.3e-48 | yxcD | S | Protein of unknown function (DUF2653) | ||
CNHFAHCC_07273 | 2.3e-246 | csbC | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07274 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
CNHFAHCC_07276 | 5.7e-152 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
CNHFAHCC_07277 | 2.2e-215 | yxbF | K | Bacterial regulatory proteins, tetR family | ||
CNHFAHCC_07278 | 1.4e-248 | alkH | 1.2.1.3 | C | Belongs to the aldehyde dehydrogenase family | |
CNHFAHCC_07279 | 1.6e-85 | yxbD | 3.2.2.20 | K | Acetyltransferase (GNAT) domain | |
CNHFAHCC_07280 | 2.2e-187 | yxbC | 1.14.11.47 | S | A domain family that is part of the cupin metalloenzyme superfamily. | |
CNHFAHCC_07281 | 3.3e-127 | yxbB | Q | Met-10+ like-protein | ||
CNHFAHCC_07282 | 4.9e-44 | S | Coenzyme PQQ synthesis protein D (PqqD) | |||
CNHFAHCC_07283 | 1.1e-86 | yxnB | ||||
CNHFAHCC_07284 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
CNHFAHCC_07285 | 7.6e-214 | yxaM | U | MFS_1 like family | ||
CNHFAHCC_07286 | 8.9e-93 | S | PQQ-like domain | |||
CNHFAHCC_07287 | 3.5e-65 | S | Family of unknown function (DUF5391) | |||
CNHFAHCC_07288 | 1.1e-75 | yxaI | S | membrane protein domain | ||
CNHFAHCC_07289 | 1.4e-228 | P | Protein of unknown function (DUF418) | |||
CNHFAHCC_07290 | 1.5e-199 | yxaG | 1.13.11.24 | S | AraC-like ligand binding domain | |
CNHFAHCC_07291 | 7.1e-101 | yxaF | K | Transcriptional regulator | ||
CNHFAHCC_07292 | 2.3e-201 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
CNHFAHCC_07293 | 4.4e-71 | yxaD | K | helix_turn_helix multiple antibiotic resistance protein | ||
CNHFAHCC_07294 | 1.4e-43 | S | LrgA family | |||
CNHFAHCC_07295 | 2.6e-118 | yxaC | M | effector of murein hydrolase | ||
CNHFAHCC_07296 | 1.3e-193 | yxaB | GM | Polysaccharide pyruvyl transferase | ||
CNHFAHCC_07297 | 7e-209 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
CNHFAHCC_07298 | 7.3e-127 | gntR | K | transcriptional | ||
CNHFAHCC_07299 | 4.6e-304 | gntK | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
CNHFAHCC_07300 | 4.6e-144 | gntP | EG | COG2610 H gluconate symporter and related permeases | ||
CNHFAHCC_07301 | 2.7e-49 | gntP | EG | COG2610 H gluconate symporter and related permeases | ||
CNHFAHCC_07302 | 3.8e-273 | gnd | 1.1.1.343, 1.1.1.44 | G | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
CNHFAHCC_07303 | 2.1e-105 | ahpC | 1.11.1.15 | O | Alkyl hydroperoxide reductase | |
CNHFAHCC_07304 | 3.8e-287 | ahpF | O | Alkyl hydroperoxide reductase | ||
CNHFAHCC_07305 | 6.4e-292 | bglA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
CNHFAHCC_07306 | 2.3e-34 | 2.7.1.199 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
CNHFAHCC_07307 | 1.3e-128 | yydK | K | Transcriptional regulator | ||
CNHFAHCC_07308 | 7.6e-13 | |||||
CNHFAHCC_07309 | 3.3e-119 | S | ABC-2 family transporter protein | |||
CNHFAHCC_07310 | 1.8e-110 | prrC | P | ABC transporter | ||
CNHFAHCC_07311 | 8.4e-134 | yydH | O | Peptidase M50 | ||
CNHFAHCC_07312 | 8e-165 | S | Radical SAM superfamily | |||
CNHFAHCC_07313 | 8e-12 | |||||
CNHFAHCC_07314 | 0.0 | fbp | 3.1.3.11 | G | Firmicute fructose-1,6-bisphosphatase | |
CNHFAHCC_07315 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2326) | |||
CNHFAHCC_07316 | 2.8e-65 | |||||
CNHFAHCC_07317 | 9.6e-280 | S | Calcineurin-like phosphoesterase | |||
CNHFAHCC_07318 | 5.2e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
CNHFAHCC_07319 | 1.1e-09 | S | YyzF-like protein | |||
CNHFAHCC_07320 | 2.2e-71 | |||||
CNHFAHCC_07321 | 3e-234 | fdhA | 1.1.1.1, 1.1.1.14, 1.1.1.284, 1.2.1.46 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
CNHFAHCC_07323 | 2.1e-33 | yycQ | S | Protein of unknown function (DUF2651) | ||
CNHFAHCC_07324 | 1.6e-221 | yycP | ||||
CNHFAHCC_07325 | 5.8e-132 | yycO | S | Permuted papain-like amidase enzyme, YaeF/YiiX, C92 family | ||
CNHFAHCC_07326 | 3.1e-86 | yycN | 2.3.1.128 | K | Acetyltransferase | |
CNHFAHCC_07327 | 5e-188 | S | aspartate phosphatase | |||
CNHFAHCC_07329 | 2.3e-167 | rocF | 3.5.3.1, 3.5.3.11 | E | Belongs to the arginase family | |
CNHFAHCC_07330 | 9.4e-253 | rocE | E | amino acid | ||
CNHFAHCC_07331 | 1.7e-234 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
CNHFAHCC_07332 | 1.5e-258 | rocR | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | ||
CNHFAHCC_07334 | 8.4e-221 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
CNHFAHCC_07335 | 8.7e-150 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
CNHFAHCC_07336 | 7.3e-155 | yycI | S | protein conserved in bacteria | ||
CNHFAHCC_07337 | 3.6e-260 | yycH | S | protein conserved in bacteria | ||
CNHFAHCC_07338 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
CNHFAHCC_07339 | 1.1e-132 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
CNHFAHCC_07345 | 1.7e-248 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
CNHFAHCC_07346 | 8e-78 | yycE | 3.4.21.26, 5.3.1.24 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
CNHFAHCC_07347 | 3e-251 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
CNHFAHCC_07348 | 1.9e-29 | yycD | S | Uncharacterized protein conserved in bacteria (DUF2188) | ||
CNHFAHCC_07350 | 1.7e-15 | yycC | K | YycC-like protein | ||
CNHFAHCC_07351 | 8.4e-221 | yeaN | P | COG2807 Cyanate permease | ||
CNHFAHCC_07352 | 0.0 | yycA | M | COG1807 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
CNHFAHCC_07353 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
CNHFAHCC_07354 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
CNHFAHCC_07355 | 2.9e-160 | yybS | S | membrane | ||
CNHFAHCC_07357 | 3.9e-84 | cotF | M | Spore coat protein | ||
CNHFAHCC_07358 | 1.4e-68 | ydeP3 | K | Transcriptional regulator | ||
CNHFAHCC_07359 | 1.1e-164 | ppaC | 3.6.1.1 | C | Inorganic pyrophosphatase | |
CNHFAHCC_07360 | 1.3e-70 | |||||
CNHFAHCC_07362 | 2.3e-240 | yybO | G | COG0477 Permeases of the major facilitator superfamily | ||
CNHFAHCC_07363 | 1e-16 | |||||
CNHFAHCC_07364 | 1e-07 | yybH | S | SnoaL-like domain | ||
CNHFAHCC_07366 | 1.3e-78 | yybN | S | Protein of unknown function (DUF2712) | ||
CNHFAHCC_07367 | 4.1e-125 | |||||
CNHFAHCC_07368 | 9e-122 | |||||
CNHFAHCC_07369 | 2e-127 | S | Protein of unknown function (DUF2705) | |||
CNHFAHCC_07370 | 2.6e-115 | V | ATPases associated with a variety of cellular activities | |||
CNHFAHCC_07371 | 6.2e-132 | |||||
CNHFAHCC_07372 | 4.8e-67 | yybH | S | SnoaL-like domain | ||
CNHFAHCC_07373 | 3e-124 | yybG | S | Pentapeptide repeat-containing protein | ||
CNHFAHCC_07374 | 3.2e-220 | ynfM | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07375 | 2.1e-165 | yybE | K | Transcriptional regulator | ||
CNHFAHCC_07376 | 2e-79 | yjcF | S | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_07377 | 2.7e-77 | yybC | ||||
CNHFAHCC_07378 | 3e-127 | S | Metallo-beta-lactamase superfamily | |||
CNHFAHCC_07379 | 5.6e-77 | yybA | 2.3.1.57 | K | transcriptional | |
CNHFAHCC_07380 | 5.9e-79 | yjcF | S | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_07381 | 1.5e-101 | yyaS | S | Membrane | ||
CNHFAHCC_07382 | 5.4e-100 | yyaR | K | Acetyltransferase (GNAT) domain | ||
CNHFAHCC_07383 | 5.4e-67 | yyaQ | S | YjbR | ||
CNHFAHCC_07384 | 1.7e-107 | yyaP | 1.5.1.3 | H | RibD C-terminal domain | |
CNHFAHCC_07385 | 1.7e-249 | tetL | EGP | Major facilitator Superfamily | ||
CNHFAHCC_07386 | 9.7e-44 | yyaL | O | Highly conserved protein containing a thioredoxin domain | ||
CNHFAHCC_07387 | 6.1e-62 | yyaN | K | MerR HTH family regulatory protein | ||
CNHFAHCC_07388 | 3.3e-161 | yyaM | EG | EamA-like transporter family | ||
CNHFAHCC_07389 | 0.0 | yyaL | O | COG1331 Highly conserved protein containing a thioredoxin domain | ||
CNHFAHCC_07390 | 9.5e-169 | yyaK | S | CAAX protease self-immunity | ||
CNHFAHCC_07391 | 2.8e-241 | EGP | Major facilitator superfamily | |||
CNHFAHCC_07392 | 5.1e-96 | maa | 2.3.1.79 | S | Bacterial transferase hexapeptide (six repeats) | |
CNHFAHCC_07393 | 4e-68 | yyaH | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
CNHFAHCC_07394 | 3.3e-180 | ccpB | 3.5.1.4, 5.1.1.1 | K | Transcriptional regulator | |
CNHFAHCC_07395 | 8.1e-145 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
CNHFAHCC_07396 | 5.1e-37 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
CNHFAHCC_07397 | 2.9e-69 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
CNHFAHCC_07398 | 4.3e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
CNHFAHCC_07399 | 4e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
CNHFAHCC_07400 | 0.0 | yyaE | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | ||
CNHFAHCC_07401 | 2.3e-33 | yyzM | S | protein conserved in bacteria | ||
CNHFAHCC_07402 | 2.9e-180 | yyaD | S | Membrane | ||
CNHFAHCC_07403 | 1.6e-111 | yyaC | S | Sporulation protein YyaC | ||
CNHFAHCC_07404 | 2.1e-149 | spo0J | K | Belongs to the ParB family | ||
CNHFAHCC_07405 | 2.2e-134 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
CNHFAHCC_07406 | 1.5e-74 | S | Bacterial PH domain | |||
CNHFAHCC_07407 | 1.9e-150 | noc | D | Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage | ||
CNHFAHCC_07408 | 2.2e-131 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 535 of 16S rRNA | |
CNHFAHCC_07409 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
CNHFAHCC_07410 | 3.1e-251 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
CNHFAHCC_07411 | 6.5e-108 | jag | S | single-stranded nucleic acid binding R3H | ||
CNHFAHCC_07412 | 1.7e-118 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
CNHFAHCC_07413 | 3e-54 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
CNHFAHCC_07414 | 4.5e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)