ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
CNGDEHKH_00001 | 1.3e-254 | 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 | ||
CNGDEHKH_00002 | 4.4e-203 | 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 | |
CNGDEHKH_00003 | 1.2e-32 | yaaA | S | S4 domain | ||
CNGDEHKH_00004 | 1.6e-205 | 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 | ||
CNGDEHKH_00005 | 7.3e-11 | yaaB | S | Domain of unknown function (DUF370) | ||
CNGDEHKH_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 | |
CNGDEHKH_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 | |
CNGDEHKH_00008 | 1.7e-196 | M1-161 | T | HD domain | ||
CNGDEHKH_00009 | 4.3e-42 | S | COG NOG14552 non supervised orthologous group | |||
CNGDEHKH_00012 | 1.7e-41 | |||||
CNGDEHKH_00013 | 3.9e-36 | csfB | S | Inhibitor of sigma-G Gin | ||
CNGDEHKH_00014 | 1.8e-289 | adiA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | Orn Lys Arg decarboxylase | |
CNGDEHKH_00015 | 2e-120 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
CNGDEHKH_00016 | 9.8e-55 | yaaQ | S | protein conserved in bacteria | ||
CNGDEHKH_00017 | 1.8e-72 | yaaR | S | protein conserved in bacteria | ||
CNGDEHKH_00018 | 4.3e-186 | holB | 2.7.7.7 | L | DNA polymerase III | |
CNGDEHKH_00019 | 1.7e-148 | yaaT | S | stage 0 sporulation protein | ||
CNGDEHKH_00020 | 4.5e-67 | yabA | L | Involved in initiation control of chromosome replication | ||
CNGDEHKH_00021 | 3.8e-139 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
CNGDEHKH_00022 | 1e-47 | yazA | L | endonuclease containing a URI domain | ||
CNGDEHKH_00023 | 2.7e-152 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
CNGDEHKH_00024 | 1.2e-56 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
CNGDEHKH_00025 | 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 | |
CNGDEHKH_00026 | 3e-147 | tatD | L | hydrolase, TatD | ||
CNGDEHKH_00027 | 8.5e-105 | 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 | |
CNGDEHKH_00028 | 2.3e-159 | 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 | |
CNGDEHKH_00029 | 8.7e-167 | yabG | S | peptidase | ||
CNGDEHKH_00030 | 2.4e-37 | veg | S | protein conserved in bacteria | ||
CNGDEHKH_00031 | 1.9e-33 | sspF | S | DNA topological change | ||
CNGDEHKH_00032 | 3.2e-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 | |
CNGDEHKH_00033 | 6.4e-154 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
CNGDEHKH_00034 | 2.7e-61 | yabJ | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | |
CNGDEHKH_00035 | 3.6e-48 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
CNGDEHKH_00037 | 3.7e-135 | S | Psort location CytoplasmicMembrane, score | |||
CNGDEHKH_00038 | 2.7e-82 | L | Transposase | |||
CNGDEHKH_00039 | 7.3e-45 | L | Transposase, IS4 family protein | |||
CNGDEHKH_00040 | 1.3e-21 | S | Psort location CytoplasmicMembrane, score | |||
CNGDEHKH_00041 | 2.9e-63 | V | ABC transporter | |||
CNGDEHKH_00042 | 2.9e-81 | |||||
CNGDEHKH_00043 | 3.5e-247 | 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 | |
CNGDEHKH_00044 | 4.3e-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) | |
CNGDEHKH_00045 | 6.3e-111 | 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 | ||
CNGDEHKH_00046 | 9.3e-106 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
CNGDEHKH_00047 | 1.7e-37 | yabK | S | Peptide ABC transporter permease | ||
CNGDEHKH_00048 | 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 | ||
CNGDEHKH_00049 | 1.8e-90 | spoVT | K | stage V sporulation protein | ||
CNGDEHKH_00050 | 3.1e-287 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
CNGDEHKH_00051 | 3.7e-196 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
CNGDEHKH_00052 | 1.1e-41 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
CNGDEHKH_00053 | 4.7e-51 | yabP | S | Sporulation protein YabP | ||
CNGDEHKH_00054 | 3.7e-111 | yabQ | S | spore cortex biosynthesis protein | ||
CNGDEHKH_00055 | 1.9e-60 | divIC | D | Septum formation initiator | ||
CNGDEHKH_00056 | 2.8e-54 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
CNGDEHKH_00058 | 0.0 | spoIIE | 3.1.3.16, 3.1.3.3 | KT | stage II sporulation protein E | |
CNGDEHKH_00059 | 4.3e-119 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
CNGDEHKH_00060 | 2e-167 | KLT | serine threonine protein kinase | |||
CNGDEHKH_00061 | 3.1e-278 | 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 | |
CNGDEHKH_00062 | 1.1e-95 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
CNGDEHKH_00063 | 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 | ||
CNGDEHKH_00064 | 1.7e-159 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
CNGDEHKH_00065 | 3e-159 | 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 | ||
CNGDEHKH_00066 | 2.6e-169 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
CNGDEHKH_00067 | 8.3e-159 | 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 | |
CNGDEHKH_00068 | 3.5e-61 | 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 | |
CNGDEHKH_00069 | 2.1e-96 | 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 | |
CNGDEHKH_00070 | 3.5e-285 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
CNGDEHKH_00071 | 4.3e-42 | S | COG NOG14552 non supervised orthologous group | |||
CNGDEHKH_00072 | 5.3e-43 | |||||
CNGDEHKH_00075 | 1.6e-08 | |||||
CNGDEHKH_00076 | 4e-08 | |||||
CNGDEHKH_00080 | 4.3e-42 | S | COG NOG14552 non supervised orthologous group | |||
CNGDEHKH_00081 | 1.6e-42 | |||||
CNGDEHKH_00082 | 1.3e-181 | yaaC | S | YaaC-like Protein | ||
CNGDEHKH_00083 | 1.5e-272 | 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 | |
CNGDEHKH_00084 | 6.5e-251 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
CNGDEHKH_00085 | 1.6e-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 | |
CNGDEHKH_00086 | 1.3e-102 | 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 | |
CNGDEHKH_00087 | 2.9e-211 | 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) | |
CNGDEHKH_00088 | 3e-248 | L | PFAM Transposase, IS4-like | |||
CNGDEHKH_00089 | 2.9e-09 | |||||
CNGDEHKH_00090 | 3.3e-126 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
CNGDEHKH_00091 | 2.9e-119 | dgk | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxyguanosine kinase | |
CNGDEHKH_00092 | 8.5e-229 | yaaH | M | Glycoside Hydrolase Family | ||
CNGDEHKH_00093 | 2.1e-88 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
CNGDEHKH_00094 | 5.3e-306 | 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 | |
CNGDEHKH_00095 | 5e-35 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
CNGDEHKH_00096 | 1.5e-109 | 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 | ||
CNGDEHKH_00097 | 3.4e-08 | yaaL | S | Protein of unknown function (DUF2508) | ||
CNGDEHKH_00098 | 4.8e-36 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
CNGDEHKH_00100 | 1.6e-210 | L | Transposase | |||
CNGDEHKH_00101 | 4.3e-42 | S | COG NOG14552 non supervised orthologous group | |||
CNGDEHKH_00104 | 5.3e-43 | |||||
CNGDEHKH_00105 | 5.4e-75 | ctsR | K | Belongs to the CtsR family | ||
CNGDEHKH_00106 | 1.3e-99 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
CNGDEHKH_00107 | 2.1e-191 | 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 | |
CNGDEHKH_00108 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
CNGDEHKH_00109 | 2.9e-254 | 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 | ||
CNGDEHKH_00110 | 6.9e-198 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
CNGDEHKH_00111 | 7.5e-118 | 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) | |
CNGDEHKH_00112 | 2.1e-82 | 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) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)