ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AHJIJCLC_00001 | 4.7e-91 | cvpA | S | Colicin V production protein | ||
AHJIJCLC_00002 | 1.6e-163 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHJIJCLC_00003 | 5.7e-33 | yrzB | S | Belongs to the UPF0473 family | ||
AHJIJCLC_00004 | 9.6e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
AHJIJCLC_00005 | 1.2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
AHJIJCLC_00006 | 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 | |
AHJIJCLC_00007 | 4.2e-232 | 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 | |
AHJIJCLC_00008 | 6.8e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
AHJIJCLC_00009 | 1.1e-39 | yajC | U | Preprotein translocase | ||
AHJIJCLC_00010 | 2.2e-176 | 2.4.2.29 | F | queuine tRNA-ribosyltransferase activity | ||
AHJIJCLC_00011 | 1.1e-189 | 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 | |
AHJIJCLC_00012 | 1.9e-104 | 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 | |
AHJIJCLC_00013 | 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 | ||
AHJIJCLC_00014 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
AHJIJCLC_00015 | 1e-202 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AHJIJCLC_00016 | 2.2e-193 | 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 | ||
AHJIJCLC_00017 | 1.9e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
AHJIJCLC_00018 | 8.5e-102 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
AHJIJCLC_00019 | 1.8e-96 | ymfM | S | Helix-turn-helix domain | ||
AHJIJCLC_00020 | 1.1e-250 | ymfH | S | Peptidase M16 | ||
AHJIJCLC_00021 | 7.3e-231 | ymfF | S | Peptidase M16 inactive domain protein | ||
AHJIJCLC_00022 | 4.1e-161 | aatB | ET | ABC transporter substrate-binding protein | ||
AHJIJCLC_00023 | 4.8e-114 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHJIJCLC_00024 | 1.4e-108 | glnP | P | ABC transporter permease | ||
AHJIJCLC_00025 | 6.6e-93 | mreD | M | rod shape-determining protein MreD | ||
AHJIJCLC_00026 | 3.7e-146 | mreC | M | Involved in formation and maintenance of cell shape | ||
AHJIJCLC_00027 | 1.9e-181 | mreB | D | cell shape determining protein MreB | ||
AHJIJCLC_00028 | 2.5e-115 | radC | L | DNA repair protein | ||
AHJIJCLC_00029 | 1.9e-250 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHJIJCLC_00030 | 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 | |
AHJIJCLC_00031 | 1.6e-88 | 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 | |
AHJIJCLC_00034 | 1.6e-36 | M | LysM domain | |||
AHJIJCLC_00035 | 1.6e-299 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
AHJIJCLC_00036 | 9.8e-163 | yvgN | C | Aldo keto reductase | ||
AHJIJCLC_00037 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AHJIJCLC_00038 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AHJIJCLC_00039 | 3.3e-280 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHJIJCLC_00040 | 0.0 | clpL | O | associated with various cellular activities | ||
AHJIJCLC_00041 | 1e-34 | |||||
AHJIJCLC_00042 | 2e-214 | patA | 2.6.1.1 | E | Aminotransferase | |
AHJIJCLC_00043 | 5.7e-183 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHJIJCLC_00044 | 1.4e-183 | D | Alpha beta | |||
AHJIJCLC_00045 | 6.2e-190 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHJIJCLC_00049 | 9.6e-25 | S | Peptidase M15A | |||
AHJIJCLC_00050 | 6.3e-28 | L | endonuclease activity | |||
AHJIJCLC_00052 | 5.3e-104 | S | structural molecule activity | |||
AHJIJCLC_00055 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AHJIJCLC_00056 | 1.5e-146 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | |
AHJIJCLC_00057 | 4.1e-130 | gntR | K | UbiC transcription regulator-associated domain protein | ||
AHJIJCLC_00058 | 7.1e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AHJIJCLC_00059 | 3.2e-130 | |||||
AHJIJCLC_00060 | 1.7e-265 | pipD | E | Dipeptidase | ||
AHJIJCLC_00061 | 2.9e-137 | L | Transposase and inactivated derivatives, IS30 family | |||
AHJIJCLC_00062 | 1.7e-271 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHJIJCLC_00063 | 3.3e-146 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
AHJIJCLC_00064 | 2.1e-157 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
AHJIJCLC_00065 | 1.5e-55 | yabA | L | Involved in initiation control of chromosome replication | ||
AHJIJCLC_00066 | 1.4e-192 | holB | 2.7.7.7 | L | DNA polymerase III | |
AHJIJCLC_00067 | 4e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
AHJIJCLC_00068 | 6e-117 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AHJIJCLC_00069 | 2.4e-21 | S | Protein of unknown function (DUF2508) | |||
AHJIJCLC_00070 | 3e-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 | ||
AHJIJCLC_00071 | 4.9e-40 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
AHJIJCLC_00072 | 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 | |
AHJIJCLC_00074 | 6.3e-80 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
AHJIJCLC_00075 | 2e-35 | nrdH | O | Glutaredoxin | ||
AHJIJCLC_00076 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHJIJCLC_00077 | 8.6e-195 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHJIJCLC_00078 | 4.1e-248 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AHJIJCLC_00080 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AHJIJCLC_00081 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AHJIJCLC_00082 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AHJIJCLC_00083 | 4.1e-176 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
AHJIJCLC_00084 | 1.1e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AHJIJCLC_00085 | 4.6e-53 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
AHJIJCLC_00086 | 8.4e-82 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
AHJIJCLC_00087 | 4.6e-244 | steT | E | amino acid | ||
AHJIJCLC_00088 | 7.4e-121 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
AHJIJCLC_00089 | 2.2e-51 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
AHJIJCLC_00090 | 4.5e-97 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
AHJIJCLC_00091 | 2.4e-23 | 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 | ||
AHJIJCLC_00092 | 3.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AHJIJCLC_00093 | 1.1e-104 | sigH | K | Belongs to the sigma-70 factor family | ||
AHJIJCLC_00094 | 2e-135 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHJIJCLC_00095 | 1.6e-70 | 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) | ||
AHJIJCLC_00096 | 1e-270 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AHJIJCLC_00097 | 7.8e-100 | ywlG | S | Belongs to the UPF0340 family | ||
AHJIJCLC_00098 | 6.2e-290 | 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) | |
AHJIJCLC_00099 | 3.2e-206 | yacL | S | domain protein | ||
AHJIJCLC_00100 | 5.6e-253 | 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 | ||
AHJIJCLC_00101 | 1.4e-98 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AHJIJCLC_00102 | 4.2e-55 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
AHJIJCLC_00103 | 6.7e-122 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AHJIJCLC_00104 | 1.1e-94 | maa | 2.3.1.18, 2.3.1.79 | S | Transferase hexapeptide repeat | |
AHJIJCLC_00105 | 4e-264 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AHJIJCLC_00106 | 9.9e-131 | opuAC | E | ABC transporter, substrate-binding protein, QAT family | ||
AHJIJCLC_00107 | 2.8e-135 | opuAB | P | glycine betaine transport system, permease | ||
AHJIJCLC_00108 | 1.4e-199 | proV | 3.6.3.32 | P | COG4175 ABC-type proline glycine betaine transport system, ATPase component | |
AHJIJCLC_00109 | 6.9e-87 | P | phosphate-selective porin O and P | |||
AHJIJCLC_00110 | 4.6e-208 | EGP | Major facilitator Superfamily | |||
AHJIJCLC_00111 | 6.1e-211 | ycsG | P | Natural resistance-associated macrophage protein | ||
AHJIJCLC_00112 | 1.7e-134 | ycsF | S | LamB/YcsF family | ||
AHJIJCLC_00113 | 1.7e-257 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
AHJIJCLC_00114 | 1.9e-58 | 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 | |
AHJIJCLC_00115 | 6.5e-190 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
AHJIJCLC_00116 | 4.6e-134 | ybgJ | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
AHJIJCLC_00117 | 9.7e-194 | ampC | V | Beta-lactamase | ||
AHJIJCLC_00118 | 1.7e-287 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AHJIJCLC_00119 | 2.8e-48 | |||||
AHJIJCLC_00120 | 3.4e-140 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
AHJIJCLC_00121 | 4.9e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AHJIJCLC_00122 | 1.2e-108 | tdk | 2.7.1.21 | F | thymidine kinase | |
AHJIJCLC_00123 | 2.5e-155 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AHJIJCLC_00124 | 7.1e-158 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
AHJIJCLC_00125 | 4.9e-193 | 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 | |
AHJIJCLC_00126 | 4.6e-230 | 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 | |
AHJIJCLC_00127 | 1.2e-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 | |
AHJIJCLC_00128 | 8.7e-188 | yibE | S | overlaps another CDS with the same product name | ||
AHJIJCLC_00129 | 3.3e-125 | yibF | S | overlaps another CDS with the same product name | ||
AHJIJCLC_00130 | 5.4e-218 | pyrP | F | Permease | ||
AHJIJCLC_00131 | 5.8e-129 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
AHJIJCLC_00132 | 1.2e-16 | 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 | ||
AHJIJCLC_00133 | 1.7e-193 | adh | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
AHJIJCLC_00134 | 2.3e-65 | lytE | M | LysM domain protein | ||
AHJIJCLC_00135 | 2.8e-85 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
AHJIJCLC_00136 | 7.7e-76 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
AHJIJCLC_00137 | 5.7e-110 | K | Transcriptional regulator, TetR family | |||
AHJIJCLC_00140 | 4e-22 | |||||
AHJIJCLC_00141 | 1.2e-67 | S | Protein of unknown function (DUF2829) | |||
AHJIJCLC_00142 | 1.2e-61 | K | DNA binding | |||
AHJIJCLC_00143 | 1.7e-116 | M | Phage head morphogenesis protein, SPP1 gp7 family | |||
AHJIJCLC_00144 | 2.7e-186 | S | Phage portal protein, SPP1 family | |||
AHJIJCLC_00145 | 7.5e-175 | S | Phage terminase large subunit | |||
AHJIJCLC_00146 | 1.4e-45 | S | DNA-packaging protein gp3 | |||
AHJIJCLC_00147 | 2.8e-07 | |||||
AHJIJCLC_00149 | 5.8e-80 | S | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_00151 | 2e-14 | M | lysozyme activity | |||
AHJIJCLC_00152 | 8.8e-194 | L | Resolvase, N terminal domain | |||
AHJIJCLC_00153 | 4.2e-39 | S | tRNA_anti-like | |||
AHJIJCLC_00156 | 3.4e-55 | S | Phage regulatory protein | |||
AHJIJCLC_00159 | 3.1e-25 | K | Helix-turn-helix domain | |||
AHJIJCLC_00168 | 1.8e-92 | S | AAA domain | |||
AHJIJCLC_00169 | 3.2e-59 | |||||
AHJIJCLC_00170 | 2.8e-69 | |||||
AHJIJCLC_00171 | 2.8e-29 | L | CHC2 zinc finger | |||
AHJIJCLC_00172 | 2.8e-149 | L | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_00173 | 2.1e-69 | rnhA | 3.1.26.4 | L | PIF1-like helicase | |
AHJIJCLC_00175 | 4.2e-49 | |||||
AHJIJCLC_00177 | 1.2e-10 | |||||
AHJIJCLC_00181 | 7.7e-11 | |||||
AHJIJCLC_00183 | 5.9e-18 | S | YopX protein | |||
AHJIJCLC_00187 | 5.8e-09 | |||||
AHJIJCLC_00189 | 5e-47 | |||||
AHJIJCLC_00192 | 2.3e-151 | xtmA | L | Terminase small subunit | ||
AHJIJCLC_00193 | 8.5e-148 | S | phage minor capsid protein | |||
AHJIJCLC_00195 | 9.5e-84 | S | Phage minor capsid protein 2 | |||
AHJIJCLC_00196 | 1.1e-41 | |||||
AHJIJCLC_00197 | 2.3e-26 | S | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_00198 | 4.2e-08 | |||||
AHJIJCLC_00199 | 7.2e-27 | |||||
AHJIJCLC_00201 | 9.5e-16 | |||||
AHJIJCLC_00202 | 8.2e-46 | |||||
AHJIJCLC_00203 | 7.1e-37 | |||||
AHJIJCLC_00206 | 2.2e-47 | S | COG NOG36366 non supervised orthologous group | |||
AHJIJCLC_00207 | 7.9e-107 | |||||
AHJIJCLC_00208 | 7.4e-22 | |||||
AHJIJCLC_00209 | 8.2e-112 | 2.1.1.72 | V | type I restriction-modification system | ||
AHJIJCLC_00210 | 2.1e-23 | S | Psort location CytoplasmicMembrane, score | |||
AHJIJCLC_00211 | 2.9e-36 | |||||
AHJIJCLC_00213 | 1.3e-34 | |||||
AHJIJCLC_00214 | 2.7e-40 | |||||
AHJIJCLC_00215 | 5.2e-08 | |||||
AHJIJCLC_00216 | 1.7e-94 | S | Bacteriophage Gp15 protein | |||
AHJIJCLC_00217 | 4.7e-175 | S | phage tail tape measure protein | |||
AHJIJCLC_00219 | 7.8e-69 | S | Phage minor structural protein | |||
AHJIJCLC_00221 | 4.6e-55 | M | autolytic lysozime (1,4-beta-N-acetylmuramidase), family 25 of glycosyl hydrolases | |||
AHJIJCLC_00222 | 8.8e-194 | L | Resolvase, N terminal domain | |||
AHJIJCLC_00223 | 4.2e-39 | S | tRNA_anti-like | |||
AHJIJCLC_00226 | 3.4e-55 | S | Phage regulatory protein | |||
AHJIJCLC_00229 | 3.1e-25 | K | Helix-turn-helix domain | |||
AHJIJCLC_00238 | 1.8e-92 | S | AAA domain | |||
AHJIJCLC_00239 | 3.2e-59 | |||||
AHJIJCLC_00240 | 2.8e-69 | |||||
AHJIJCLC_00241 | 2.8e-29 | L | CHC2 zinc finger | |||
AHJIJCLC_00242 | 2.8e-149 | L | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_00243 | 2.1e-69 | rnhA | 3.1.26.4 | L | PIF1-like helicase | |
AHJIJCLC_00245 | 4.2e-49 | |||||
AHJIJCLC_00247 | 1.2e-10 | |||||
AHJIJCLC_00251 | 7.7e-11 | |||||
AHJIJCLC_00253 | 5.9e-18 | S | YopX protein | |||
AHJIJCLC_00257 | 5.8e-09 | |||||
AHJIJCLC_00259 | 5e-47 | |||||
AHJIJCLC_00262 | 2.3e-151 | xtmA | L | Terminase small subunit | ||
AHJIJCLC_00263 | 8.5e-148 | S | phage minor capsid protein | |||
AHJIJCLC_00265 | 9.5e-84 | S | Phage minor capsid protein 2 | |||
AHJIJCLC_00266 | 1.1e-41 | |||||
AHJIJCLC_00267 | 2.3e-26 | S | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_00268 | 4.2e-08 | |||||
AHJIJCLC_00269 | 7.2e-27 | |||||
AHJIJCLC_00271 | 9.5e-16 | |||||
AHJIJCLC_00272 | 8.2e-46 | |||||
AHJIJCLC_00273 | 7.1e-37 | |||||
AHJIJCLC_00276 | 2.2e-47 | S | COG NOG36366 non supervised orthologous group | |||
AHJIJCLC_00277 | 7.9e-107 | |||||
AHJIJCLC_00278 | 7.4e-22 | |||||
AHJIJCLC_00279 | 8.2e-112 | 2.1.1.72 | V | type I restriction-modification system | ||
AHJIJCLC_00280 | 2.1e-23 | S | Psort location CytoplasmicMembrane, score | |||
AHJIJCLC_00281 | 2.9e-36 | |||||
AHJIJCLC_00283 | 1.3e-34 | |||||
AHJIJCLC_00284 | 2.7e-40 | |||||
AHJIJCLC_00285 | 5.2e-08 | |||||
AHJIJCLC_00286 | 1.7e-94 | S | Bacteriophage Gp15 protein | |||
AHJIJCLC_00287 | 4.7e-175 | S | phage tail tape measure protein | |||
AHJIJCLC_00291 | 1.2e-110 | S | VIT family | |||
AHJIJCLC_00292 | 9.4e-116 | S | membrane | |||
AHJIJCLC_00293 | 7.1e-164 | czcD | P | cation diffusion facilitator family transporter | ||
AHJIJCLC_00294 | 3.1e-124 | sirR | K | iron dependent repressor | ||
AHJIJCLC_00295 | 1.3e-30 | cspA | K | Cold shock protein | ||
AHJIJCLC_00296 | 2.6e-127 | thrE | S | Putative threonine/serine exporter | ||
AHJIJCLC_00297 | 2.8e-82 | S | Threonine/Serine exporter, ThrE | |||
AHJIJCLC_00298 | 9.1e-116 | lssY | 3.6.1.27 | I | phosphatase | |
AHJIJCLC_00299 | 1.2e-154 | I | alpha/beta hydrolase fold | |||
AHJIJCLC_00301 | 2.6e-236 | kgtP | EGP | Sugar (and other) transporter | ||
AHJIJCLC_00302 | 7.4e-29 | M | domain protein | |||
AHJIJCLC_00303 | 2.2e-27 | |||||
AHJIJCLC_00304 | 1.1e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
AHJIJCLC_00305 | 3.5e-158 | noc | K | Belongs to the ParB family | ||
AHJIJCLC_00306 | 2.1e-146 | spo0J | K | Belongs to the ParB family | ||
AHJIJCLC_00307 | 9.3e-32 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
AHJIJCLC_00308 | 1.3e-199 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
AHJIJCLC_00309 | 7.7e-135 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
AHJIJCLC_00310 | 4.5e-208 | guaB | 1.1.1.205 | 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 | |
AHJIJCLC_00311 | 4e-168 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AHJIJCLC_00312 | 2.1e-132 | epsB | M | biosynthesis protein | ||
AHJIJCLC_00313 | 1.4e-114 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
AHJIJCLC_00314 | 1e-139 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
AHJIJCLC_00315 | 4.1e-83 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
AHJIJCLC_00316 | 3.4e-171 | L | Integrase core domain | |||
AHJIJCLC_00317 | 7.3e-46 | L | Transposase | |||
AHJIJCLC_00318 | 7.1e-264 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
AHJIJCLC_00319 | 1.3e-75 | 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 | |
AHJIJCLC_00320 | 1.6e-63 | 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 | |
AHJIJCLC_00321 | 1.3e-229 | 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 | |
AHJIJCLC_00322 | 1e-128 | IQ | reductase | |||
AHJIJCLC_00323 | 1.1e-172 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
AHJIJCLC_00324 | 4.2e-34 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
AHJIJCLC_00325 | 8.9e-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 | |
AHJIJCLC_00326 | 2.3e-75 | marR | K | Transcriptional regulator, MarR family | ||
AHJIJCLC_00327 | 1.3e-75 | 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 | |
AHJIJCLC_00329 | 1.2e-194 | 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 | |
AHJIJCLC_00330 | 1.3e-110 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
AHJIJCLC_00331 | 2.2e-131 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
AHJIJCLC_00332 | 2.2e-215 | arcT | 2.6.1.1 | E | Aminotransferase | |
AHJIJCLC_00333 | 2.7e-221 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
AHJIJCLC_00334 | 2.7e-258 | E | Arginine ornithine antiporter | |||
AHJIJCLC_00335 | 8.2e-240 | arcA | 3.5.3.6 | E | Arginine | |
AHJIJCLC_00336 | 1.4e-167 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
AHJIJCLC_00337 | 6e-188 | 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 | |
AHJIJCLC_00338 | 2.4e-145 | KT | YcbB domain | |||
AHJIJCLC_00339 | 1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
AHJIJCLC_00340 | 7e-49 | 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 | ||
AHJIJCLC_00341 | 1.9e-219 | lysP | E | amino acid | ||
AHJIJCLC_00342 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
AHJIJCLC_00343 | 3e-292 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
AHJIJCLC_00344 | 1.8e-292 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
AHJIJCLC_00345 | 1.9e-112 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AHJIJCLC_00346 | 4.9e-224 | 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 | |
AHJIJCLC_00347 | 1.1e-139 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
AHJIJCLC_00348 | 3.3e-209 | 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 | |
AHJIJCLC_00349 | 5e-51 | |||||
AHJIJCLC_00350 | 1.7e-96 | tag | 3.2.2.20 | L | glycosylase | |
AHJIJCLC_00351 | 7.8e-203 | EGP | Major facilitator Superfamily | |||
AHJIJCLC_00352 | 3.6e-78 | 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 | |
AHJIJCLC_00353 | 2.4e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
AHJIJCLC_00354 | 2.9e-81 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
AHJIJCLC_00355 | 7.3e-89 | K | Acetyltransferase (GNAT) domain | |||
AHJIJCLC_00356 | 1.3e-101 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
AHJIJCLC_00357 | 5.7e-166 | murB | 1.3.1.98 | M | Cell wall formation | |
AHJIJCLC_00358 | 7.8e-149 | 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 | |
AHJIJCLC_00359 | 9.1e-116 | ybbR | S | YbbR-like protein | ||
AHJIJCLC_00360 | 2.5e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
AHJIJCLC_00361 | 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 | |
AHJIJCLC_00362 | 3.3e-52 | |||||
AHJIJCLC_00363 | 5.4e-211 | oatA | I | Acyltransferase | ||
AHJIJCLC_00364 | 2.6e-149 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
AHJIJCLC_00365 | 2.4e-75 | lytE | M | Lysin motif | ||
AHJIJCLC_00366 | 1.3e-158 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
AHJIJCLC_00367 | 2.8e-168 | K | LysR substrate binding domain | |||
AHJIJCLC_00368 | 1.7e-131 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
AHJIJCLC_00369 | 1.3e-148 | yitS | S | EDD domain protein, DegV family | ||
AHJIJCLC_00370 | 6.5e-90 | racA | K | Domain of unknown function (DUF1836) | ||
AHJIJCLC_00371 | 2.3e-181 | yfeX | P | Peroxidase | ||
AHJIJCLC_00372 | 5.3e-181 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
AHJIJCLC_00373 | 2.7e-122 | manY | G | PTS system | ||
AHJIJCLC_00374 | 7.4e-169 | manN | G | system, mannose fructose sorbose family IID component | ||
AHJIJCLC_00375 | 2.3e-56 | S | Domain of unknown function (DUF956) | |||
AHJIJCLC_00377 | 0.0 | rnjA | J | 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 | ||
AHJIJCLC_00378 | 1.5e-58 | |||||
AHJIJCLC_00379 | 1.9e-74 | merR | K | MerR HTH family regulatory protein | ||
AHJIJCLC_00380 | 1.1e-267 | lmrB | EGP | Major facilitator Superfamily | ||
AHJIJCLC_00381 | 6.1e-33 | U | EntS YbdA MFS transporter | |||
AHJIJCLC_00382 | 1.4e-07 | U | Parallel beta-helix repeats | |||
AHJIJCLC_00383 | 3.8e-185 | M | Psort location Cellwall, score | |||
AHJIJCLC_00384 | 7.5e-216 | M | Psort location Cellwall, score | |||
AHJIJCLC_00385 | 8.7e-84 | 3.4.22.70 | M | Sortase family | ||
AHJIJCLC_00386 | 2.4e-29 | |||||
AHJIJCLC_00387 | 2.6e-46 | srtB | 3.4.22.70 | S | sortase, SrtB family | |
AHJIJCLC_00389 | 1.8e-21 | S | cell division cycle 2-like 6 (CDK8-like) | |||
AHJIJCLC_00392 | 3.2e-19 | S | Psort location CytoplasmicMembrane, score 9.26 | |||
AHJIJCLC_00393 | 1.3e-58 | S | Psort location CytoplasmicMembrane, score | |||
AHJIJCLC_00394 | 1.4e-12 | S | PrgI family protein | |||
AHJIJCLC_00395 | 6.6e-295 | U | type IV secretory pathway VirB4 | |||
AHJIJCLC_00396 | 2e-51 | spr | M | CHAP domain | ||
AHJIJCLC_00399 | 8.6e-13 | K | Helix-turn-helix XRE-family like proteins | |||
AHJIJCLC_00400 | 5.2e-121 | L | Transposase IS116/IS110/IS902 family | |||
AHJIJCLC_00401 | 1.4e-44 | mdtG | EGP | Major facilitator Superfamily | ||
AHJIJCLC_00402 | 5.8e-50 | mdtG | EGP | Major facilitator Superfamily | ||
AHJIJCLC_00403 | 6e-41 | rpmE2 | J | Ribosomal protein L31 | ||
AHJIJCLC_00404 | 5.2e-237 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
AHJIJCLC_00405 | 4.4e-311 | 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 | |
AHJIJCLC_00406 | 1.6e-47 | 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 | ||
AHJIJCLC_00407 | 3.2e-74 | ywiB | S | Domain of unknown function (DUF1934) | ||
AHJIJCLC_00408 | 4.3e-266 | ywfO | S | HD domain protein | ||
AHJIJCLC_00409 | 4.8e-143 | yxeH | S | hydrolase | ||
AHJIJCLC_00410 | 3e-32 | |||||
AHJIJCLC_00411 | 6.1e-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) | |
AHJIJCLC_00412 | 2.8e-204 | 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 | |
AHJIJCLC_00413 | 7.5e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
AHJIJCLC_00414 | 3.2e-128 | znuB | U | ABC 3 transport family | ||
AHJIJCLC_00415 | 3.9e-93 | fhuC | P | ABC transporter | ||
AHJIJCLC_00416 | 1.2e-58 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AHJIJCLC_00417 | 2.3e-59 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
AHJIJCLC_00418 | 0.0 | XK27_08315 | M | Sulfatase | ||
AHJIJCLC_00419 | 2.7e-139 | yihY | S | Belongs to the UPF0761 family | ||
AHJIJCLC_00420 | 3.8e-31 | S | Protein of unknown function (DUF2922) | |||
AHJIJCLC_00421 | 1.3e-07 | |||||
AHJIJCLC_00422 | 5.5e-147 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
AHJIJCLC_00423 | 1.1e-118 | rfbP | M | Bacterial sugar transferase | ||
AHJIJCLC_00424 | 0.0 | yjcE | P | Sodium proton antiporter | ||
AHJIJCLC_00425 | 1.2e-16 | yvlA | ||||
AHJIJCLC_00426 | 2.2e-114 | P | Cobalt transport protein | |||
AHJIJCLC_00427 | 3.7e-257 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
AHJIJCLC_00428 | 1.3e-99 | S | ABC-type cobalt transport system, permease component | |||
AHJIJCLC_00429 | 2e-180 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
AHJIJCLC_00430 | 4.4e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
AHJIJCLC_00431 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
AHJIJCLC_00432 | 2.5e-33 | copZ | P | Heavy-metal-associated domain | ||
AHJIJCLC_00433 | 9.8e-100 | dps | P | Belongs to the Dps family | ||
AHJIJCLC_00434 | 2.8e-106 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
AHJIJCLC_00435 | 2e-85 | |||||
AHJIJCLC_00436 | 5.1e-259 | L | Transposase IS66 family | |||
AHJIJCLC_00437 | 1e-81 | uspA | T | universal stress protein | ||
AHJIJCLC_00438 | 1.9e-77 | K | AsnC family | |||
AHJIJCLC_00439 | 4.6e-140 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
AHJIJCLC_00440 | 3.1e-101 | MA20_03535 | 1.1.1.399, 1.1.1.95 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHJIJCLC_00441 | 4.7e-177 | K | helix_turn _helix lactose operon repressor | |||
AHJIJCLC_00442 | 8.2e-111 | pepF | E | oligoendopeptidase F | ||
AHJIJCLC_00443 | 6.1e-196 | 6.3.1.20 | H | Lipoate-protein ligase | ||
AHJIJCLC_00444 | 2.3e-248 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AHJIJCLC_00445 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
AHJIJCLC_00446 | 8.1e-207 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AHJIJCLC_00447 | 2.8e-246 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AHJIJCLC_00448 | 8.9e-181 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AHJIJCLC_00449 | 1.2e-73 | ycsI | S | Protein of unknown function (DUF1445) | ||
AHJIJCLC_00451 | 1.1e-223 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AHJIJCLC_00452 | 3.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AHJIJCLC_00453 | 9.2e-98 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AHJIJCLC_00454 | 1.1e-116 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
AHJIJCLC_00455 | 9.6e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
AHJIJCLC_00456 | 1.2e-180 | glk | 2.7.1.2 | G | Glucokinase | |
AHJIJCLC_00457 | 1.5e-71 | yqhL | P | Rhodanese-like protein | ||
AHJIJCLC_00458 | 4.8e-24 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
AHJIJCLC_00459 | 3.2e-172 | miaA | 2.5.1.75 | F | 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) | |
AHJIJCLC_00460 | 7.6e-139 | P | phosphate-selective porin O and P | |||
AHJIJCLC_00461 | 5e-163 | proV | 3.6.3.32 | P | COG4175 ABC-type proline glycine betaine transport system, ATPase component | |
AHJIJCLC_00462 | 3.2e-118 | opuAB | P | glycine betaine transport system, permease | ||
AHJIJCLC_00463 | 1.1e-108 | opuAC | E | ABC transporter, substrate-binding protein, QAT family | ||
AHJIJCLC_00464 | 1.4e-22 | kamA | 5.4.3.2 | C | Lysine 2,3-aminomutase | |
AHJIJCLC_00465 | 3e-184 | fruR3 | K | Transcriptional regulator, LacI family | ||
AHJIJCLC_00466 | 1.1e-161 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
AHJIJCLC_00467 | 7.7e-166 | rbsK | 2.7.1.15 | 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 | |
AHJIJCLC_00468 | 1e-56 | trxA1 | O | Belongs to the thioredoxin family | ||
AHJIJCLC_00469 | 5.2e-142 | terC | P | membrane | ||
AHJIJCLC_00470 | 9.3e-169 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AHJIJCLC_00471 | 1e-170 | corA | P | CorA-like Mg2+ transporter protein | ||
AHJIJCLC_00473 | 6.2e-86 | M | COG3209 Rhs family protein | |||
AHJIJCLC_00474 | 1.3e-179 | S | Psort location OuterMembrane, score | |||
AHJIJCLC_00475 | 5.6e-95 | P | Imelysin | |||
AHJIJCLC_00476 | 7.4e-221 | C | Di-haem oxidoreductase, putative peroxidase | |||
AHJIJCLC_00477 | 1.6e-179 | P | Psort location OuterMembrane, score | |||
AHJIJCLC_00478 | 1e-48 | |||||
AHJIJCLC_00479 | 4.3e-182 | J | endoribonuclease L-PSP | |||
AHJIJCLC_00480 | 3.2e-46 | S | Toxin SymE, type I toxin-antitoxin system | |||
AHJIJCLC_00481 | 6.7e-254 | |||||
AHJIJCLC_00482 | 0.0 | |||||
AHJIJCLC_00483 | 1.2e-58 | |||||
AHJIJCLC_00484 | 4.8e-270 | S | Phage-related minor tail protein | |||
AHJIJCLC_00485 | 3.5e-21 | |||||
AHJIJCLC_00486 | 1.4e-65 | S | Psort location Cytoplasmic, score | |||
AHJIJCLC_00487 | 4.7e-87 | S | phage major tail protein, phi13 family | |||
AHJIJCLC_00488 | 3.7e-51 | |||||
AHJIJCLC_00489 | 4e-60 | S | Bacteriophage HK97-gp10, putative tail-component | |||
AHJIJCLC_00490 | 1.6e-55 | S | Phage head-tail joining protein | |||
AHJIJCLC_00491 | 8.1e-39 | S | Phage gp6-like head-tail connector protein | |||
AHJIJCLC_00492 | 1.2e-219 | S | Phage capsid family | |||
AHJIJCLC_00493 | 2.8e-130 | clpP | 3.4.21.92 | OU | Serine dehydrogenase proteinase | |
AHJIJCLC_00494 | 8.8e-101 | K | helix_turn_helix multiple antibiotic resistance protein | |||
AHJIJCLC_00495 | 1e-64 | fsr | EGP | Major Facilitator Superfamily | ||
AHJIJCLC_00496 | 2.8e-47 | fsr | EGP | Major Facilitator Superfamily | ||
AHJIJCLC_00497 | 9.2e-100 | ogt | 2.1.1.63, 3.2.2.20 | 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 | |
AHJIJCLC_00498 | 2.7e-103 | S | CAAX protease self-immunity | |||
AHJIJCLC_00500 | 8.2e-120 | Q | Methyltransferase domain | |||
AHJIJCLC_00501 | 9.6e-90 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
AHJIJCLC_00502 | 2.8e-51 | K | 2 iron, 2 sulfur cluster binding | |||
AHJIJCLC_00503 | 0.0 | mco | Q | Multicopper oxidase | ||
AHJIJCLC_00504 | 7.1e-89 | S | Aminoacyl-tRNA editing domain | |||
AHJIJCLC_00505 | 1.2e-74 | ddaH | 3.5.3.18 | E | Amidinotransferase | |
AHJIJCLC_00507 | 3.9e-193 | nhaC | C | Na H antiporter NhaC | ||
AHJIJCLC_00508 | 1.9e-186 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
AHJIJCLC_00509 | 2.2e-51 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
AHJIJCLC_00510 | 1.6e-27 | S | FRG domain protein | |||
AHJIJCLC_00511 | 3e-116 | G | Domain of unknown function (DUF3473) | |||
AHJIJCLC_00513 | 1.5e-14 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | |||
AHJIJCLC_00514 | 2.8e-184 | Q | FkbH domain protein | |||
AHJIJCLC_00515 | 7.9e-46 | 5.1.99.1 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
AHJIJCLC_00516 | 7.1e-123 | fabH | 2.3.1.180 | I | 3-Oxoacyl-[acyl-carrier-protein (ACP)] synthase III C terminal | |
AHJIJCLC_00517 | 2.1e-36 | IQ | COGs COG1028 Dehydrogenase with different specificities (related to short-chain alcohol dehydrogenase) | |||
AHJIJCLC_00518 | 2.9e-20 | IQ | Phosphopantetheine attachment site | |||
AHJIJCLC_00519 | 1.1e-66 | M | LicD family | |||
AHJIJCLC_00520 | 2.1e-98 | eps4I | GM | Male sterility protein | ||
AHJIJCLC_00521 | 1.8e-114 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase | |
AHJIJCLC_00522 | 1.2e-42 | cpsIaJ | S | Glycosyltransferase like family 2 | ||
AHJIJCLC_00523 | 2.2e-24 | S | EpsG family | |||
AHJIJCLC_00524 | 1.9e-200 | S | Polysaccharide biosynthesis protein | |||
AHJIJCLC_00525 | 7.9e-205 | wecA | 2.7.8.33, 2.7.8.35, 5.1.3.14 | M | UDP-N-acetylmuramyl pentapeptide phosphotransferase | |
AHJIJCLC_00527 | 1e-273 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
AHJIJCLC_00530 | 7.8e-229 | yjmB | G | MFS/sugar transport protein | ||
AHJIJCLC_00531 | 4.5e-246 | 5.1.2.7 | S | tagaturonate epimerase | ||
AHJIJCLC_00532 | 3.9e-241 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
AHJIJCLC_00533 | 2.1e-45 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
AHJIJCLC_00534 | 2.4e-84 | kdgR | K | FCD domain | ||
AHJIJCLC_00535 | 6.8e-124 | V | Polysaccharide biosynthesis C-terminal domain | |||
AHJIJCLC_00537 | 8.7e-217 | gph | G | MFS/sugar transport protein | ||
AHJIJCLC_00538 | 0.0 | yicI | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
AHJIJCLC_00539 | 3.6e-218 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
AHJIJCLC_00540 | 4.5e-123 | yqhA | G | Aldose 1-epimerase | ||
AHJIJCLC_00541 | 1.4e-120 | G | Glycosyl hydrolases family 28 | |||
AHJIJCLC_00542 | 2.3e-195 | gudD | 4.2.1.40 | M | Mandelate racemase / muconate lactonizing enzyme, C-terminal domain | |
AHJIJCLC_00543 | 6.7e-251 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
AHJIJCLC_00544 | 3.4e-230 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
AHJIJCLC_00545 | 3.2e-115 | exuR | K | Periplasmic binding protein domain | ||
AHJIJCLC_00546 | 4.1e-53 | KT | PspC domain protein | |||
AHJIJCLC_00547 | 1.2e-47 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
AHJIJCLC_00548 | 2.7e-177 | 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. Therefore, by controlling the phosphorylation state of HPr, 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 | ||
AHJIJCLC_00549 | 1.1e-161 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
AHJIJCLC_00550 | 5.3e-184 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AHJIJCLC_00551 | 2.1e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
AHJIJCLC_00552 | 7.5e-146 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
AHJIJCLC_00553 | 1.1e-225 | mtnE | 2.6.1.83 | E | Aminotransferase | |
AHJIJCLC_00554 | 5.8e-188 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AHJIJCLC_00555 | 5.8e-76 | yphH | S | Cupin domain | ||
AHJIJCLC_00556 | 2.9e-103 | dedA | S | SNARE-like domain protein | ||
AHJIJCLC_00557 | 5.7e-25 | S | Protein of unknown function (DUF1461) | |||
AHJIJCLC_00558 | 6.6e-142 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
AHJIJCLC_00559 | 1.2e-97 | yutD | S | Protein of unknown function (DUF1027) | ||
AHJIJCLC_00560 | 2e-109 | S | Calcineurin-like phosphoesterase | |||
AHJIJCLC_00561 | 2.1e-224 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AHJIJCLC_00562 | 8.6e-159 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AHJIJCLC_00564 | 1e-14 | |||||
AHJIJCLC_00566 | 2.3e-15 | NU | general secretion pathway protein | |||
AHJIJCLC_00567 | 1.1e-47 | comGC | U | competence protein ComGC | ||
AHJIJCLC_00568 | 7.8e-159 | comGB | NU | type II secretion system | ||
AHJIJCLC_00569 | 7.7e-177 | comGA | NU | Type II IV secretion system protein | ||
AHJIJCLC_00570 | 1.3e-86 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
AHJIJCLC_00571 | 2.5e-97 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
AHJIJCLC_00572 | 9.2e-83 | mltD | CBM50 | M | PFAM NLP P60 protein | |
AHJIJCLC_00573 | 3.7e-134 | yebC | K | Transcriptional regulatory protein | ||
AHJIJCLC_00574 | 3.6e-85 | |||||
AHJIJCLC_00575 | 2.2e-185 | ccpA | K | catabolite control protein A | ||
AHJIJCLC_00576 | 7.7e-213 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AHJIJCLC_00577 | 4.9e-70 | |||||
AHJIJCLC_00578 | 2.7e-25 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
AHJIJCLC_00579 | 4e-156 | ykuT | M | mechanosensitive ion channel | ||
AHJIJCLC_00580 | 1.4e-150 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | ||
AHJIJCLC_00581 | 1.4e-95 | S | Phosphoesterase | |||
AHJIJCLC_00582 | 3.6e-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 | |
AHJIJCLC_00583 | 6.3e-148 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AHJIJCLC_00584 | 1.6e-94 | yslB | S | Protein of unknown function (DUF2507) | ||
AHJIJCLC_00585 | 1.2e-225 | clcA_2 | P | Chloride transporter, ClC family | ||
AHJIJCLC_00586 | 7.6e-32 | trxA | O | Belongs to the thioredoxin family | ||
AHJIJCLC_00587 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AHJIJCLC_00588 | 1.4e-167 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
AHJIJCLC_00589 | 7.7e-154 | yitU | 3.1.3.104 | S | hydrolase | |
AHJIJCLC_00590 | 0.0 | narH | 1.7.5.1 | C | Respiratory nitrate reductase beta C-terminal | |
AHJIJCLC_00591 | 3.1e-102 | narJ | C | Nitrate reductase delta subunit | ||
AHJIJCLC_00592 | 4e-127 | narI | 1.7.5.1 | C | Nitrate reductase | |
AHJIJCLC_00593 | 5e-184 | |||||
AHJIJCLC_00594 | 1.3e-75 | |||||
AHJIJCLC_00595 | 6e-113 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
AHJIJCLC_00596 | 8.6e-116 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
AHJIJCLC_00597 | 3.6e-111 | |||||
AHJIJCLC_00598 | 9.9e-183 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
AHJIJCLC_00599 | 9e-119 | S | CAAX protease self-immunity | |||
AHJIJCLC_00600 | 2.5e-62 | 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 | |
AHJIJCLC_00601 | 1.5e-94 | 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 | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
AHJIJCLC_00602 | 1.5e-103 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
AHJIJCLC_00603 | 2.2e-243 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AHJIJCLC_00604 | 1.2e-106 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
AHJIJCLC_00606 | 3.4e-240 | dtpT | U | amino acid peptide transporter | ||
AHJIJCLC_00608 | 2.4e-212 | ydiN | G | Major Facilitator Superfamily | ||
AHJIJCLC_00609 | 7.6e-13 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase type II | |
AHJIJCLC_00610 | 7.4e-214 | 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 | |
AHJIJCLC_00611 | 3.2e-103 | |||||
AHJIJCLC_00612 | 1.3e-11 | S | YjcQ protein | |||
AHJIJCLC_00613 | 4.6e-149 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
AHJIJCLC_00614 | 2.4e-133 | S | Membrane | |||
AHJIJCLC_00615 | 1.3e-75 | 4.4.1.5 | E | Glyoxalase | ||
AHJIJCLC_00616 | 1.5e-85 | yueI | S | Protein of unknown function (DUF1694) | ||
AHJIJCLC_00617 | 2.2e-235 | rarA | L | recombination factor protein RarA | ||
AHJIJCLC_00619 | 6.8e-81 | usp6 | T | universal stress protein | ||
AHJIJCLC_00620 | 7.1e-150 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
AHJIJCLC_00621 | 7.7e-216 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
AHJIJCLC_00622 | 5.3e-181 | S | Protein of unknown function (DUF2785) | |||
AHJIJCLC_00624 | 5.8e-222 | rodA | D | Belongs to the SEDS family | ||
AHJIJCLC_00625 | 7.9e-32 | S | Protein of unknown function (DUF2969) | |||
AHJIJCLC_00626 | 2.6e-183 | mbl | D | Cell shape determining protein MreB Mrl | ||
AHJIJCLC_00627 | 2.1e-219 | murA | 2.5.1.7 | M | EPSP synthase (3-phosphoshikimate 1-carboxyvinyltransferase) | |
AHJIJCLC_00628 | 2.8e-29 | S | Protein of unknown function (DUF1146) | |||
AHJIJCLC_00629 | 4.4e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AHJIJCLC_00630 | 4.4e-253 | 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 | |
AHJIJCLC_00631 | 2.3e-165 | 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 | ||
AHJIJCLC_00632 | 4e-284 | 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 | |
AHJIJCLC_00633 | 3.7e-91 | 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 | ||
AHJIJCLC_00634 | 4.4e-56 | 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 | |
AHJIJCLC_00635 | 3.1e-220 | purK2 | 6.3.4.18 | 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 | |
AHJIJCLC_00636 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
AHJIJCLC_00637 | 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 | |
AHJIJCLC_00638 | 3.2e-166 | camS | S | sex pheromone | ||
AHJIJCLC_00639 | 1e-48 | 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) | |
AHJIJCLC_00640 | 2e-272 | 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) | |
AHJIJCLC_00641 | 5e-273 | 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) | |
AHJIJCLC_00642 | 4.8e-185 | yegS | 2.7.1.107 | G | Lipid kinase | |
AHJIJCLC_00643 | 2e-263 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHJIJCLC_00644 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
AHJIJCLC_00645 | 0.0 | norZ | 1.7.2.5 | P | Cytochrome C and Quinol oxidase polypeptide I | |
AHJIJCLC_00647 | 5.1e-93 | K | Transcriptional regulator (TetR family) | |||
AHJIJCLC_00648 | 4e-187 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AHJIJCLC_00649 | 4.4e-169 | |||||
AHJIJCLC_00651 | 3.4e-82 | zur | P | Belongs to the Fur family | ||
AHJIJCLC_00652 | 1.7e-105 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
AHJIJCLC_00653 | 1.3e-72 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
AHJIJCLC_00654 | 8.8e-206 | yfnA | E | Amino Acid | ||
AHJIJCLC_00655 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
AHJIJCLC_00656 | 4e-178 | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | ||
AHJIJCLC_00657 | 6.6e-116 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
AHJIJCLC_00658 | 1.4e-272 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AHJIJCLC_00659 | 1.2e-182 | 1.17.4.1 | F | Ribonucleotide reductase, small chain | ||
AHJIJCLC_00660 | 8.8e-170 | nrdF | 1.17.4.1 | F | Ribonucleotide reductase, small chain | |
AHJIJCLC_00661 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
AHJIJCLC_00662 | 3.1e-83 | nrdI | F | NrdI Flavodoxin like | ||
AHJIJCLC_00663 | 5.1e-110 | M | ErfK YbiS YcfS YnhG | |||
AHJIJCLC_00665 | 9.8e-205 | nrnB | S | DHHA1 domain | ||
AHJIJCLC_00666 | 3.4e-291 | S | ABC transporter, ATP-binding protein | |||
AHJIJCLC_00667 | 5.9e-180 | ABC-SBP | S | ABC transporter | ||
AHJIJCLC_00668 | 8.7e-138 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
AHJIJCLC_00669 | 1.4e-133 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
AHJIJCLC_00671 | 9.7e-225 | amtB | P | ammonium transporter | ||
AHJIJCLC_00672 | 8.6e-235 | mepA | V | MATE efflux family protein | ||
AHJIJCLC_00673 | 2.2e-170 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
AHJIJCLC_00674 | 1.6e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AHJIJCLC_00675 | 6.4e-78 | trpD | 2.4.2.18, 2.6.1.85, 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) | |
AHJIJCLC_00676 | 1.3e-223 | 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 | |
AHJIJCLC_00677 | 3.7e-176 | T | PhoQ Sensor | |||
AHJIJCLC_00678 | 2.1e-105 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
AHJIJCLC_00679 | 7.7e-106 | L | transposase, IS605 OrfB family | |||
AHJIJCLC_00680 | 2.9e-52 | tlpA2 | L | Transposase IS200 like | ||
AHJIJCLC_00681 | 3.6e-296 | ybeC | E | amino acid | ||
AHJIJCLC_00682 | 1.2e-134 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHJIJCLC_00683 | 1.6e-146 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
AHJIJCLC_00684 | 1e-15 | |||||
AHJIJCLC_00685 | 1e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
AHJIJCLC_00686 | 7.3e-225 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
AHJIJCLC_00687 | 3.1e-144 | 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) | |
AHJIJCLC_00688 | 1e-248 | 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 | |
AHJIJCLC_00689 | 1.5e-253 | yifK | E | Amino acid permease | ||
AHJIJCLC_00690 | 2.2e-290 | clcA | P | chloride | ||
AHJIJCLC_00691 | 7.7e-33 | secG | U | Preprotein translocase | ||
AHJIJCLC_00692 | 2.6e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
AHJIJCLC_00693 | 8.7e-119 | 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 | ||
AHJIJCLC_00694 | 2.7e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
AHJIJCLC_00695 | 4.8e-45 | 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 | ||
AHJIJCLC_00696 | 3.2e-150 | 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 | ||
AHJIJCLC_00697 | 8.4e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
AHJIJCLC_00698 | 2.2e-52 | 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 | ||
AHJIJCLC_00699 | 6.2e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
AHJIJCLC_00700 | 6e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
AHJIJCLC_00701 | 1.1e-27 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
AHJIJCLC_00702 | 6.5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
AHJIJCLC_00703 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
AHJIJCLC_00704 | 5.2e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
AHJIJCLC_00705 | 4.2e-95 | 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 | ||
AHJIJCLC_00706 | 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 | ||
AHJIJCLC_00707 | 1e-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 | ||
AHJIJCLC_00708 | 5.1e-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 | ||
AHJIJCLC_00709 | 3.9e-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 | ||
AHJIJCLC_00710 | 2.6e-86 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
AHJIJCLC_00711 | 2.5e-23 | rpmD | J | Ribosomal protein L30 | ||
AHJIJCLC_00712 | 2.1e-65 | rplO | J | Binds to the 23S rRNA | ||
AHJIJCLC_00713 | 5.8e-236 | 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 | ||
AHJIJCLC_00714 | 6.4e-122 | 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 | |
AHJIJCLC_00715 | 2e-32 | 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 | ||
AHJIJCLC_00716 | 1.1e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
AHJIJCLC_00717 | 9.5e-59 | 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 | ||
AHJIJCLC_00718 | 1e-63 | 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 | ||
AHJIJCLC_00719 | 2e-169 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
AHJIJCLC_00720 | 2.8e-61 | rplQ | J | Ribosomal protein L17 | ||
AHJIJCLC_00721 | 1.7e-148 | 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 | ||
AHJIJCLC_00722 | 2e-155 | 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 | |
AHJIJCLC_00723 | 1.1e-139 | ecfT | U | 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 | ||
AHJIJCLC_00724 | 6.3e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
AHJIJCLC_00725 | 2.6e-79 | 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 | ||
AHJIJCLC_00726 | 1.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
AHJIJCLC_00727 | 1.2e-09 | K | Cro/C1-type HTH DNA-binding domain | |||
AHJIJCLC_00728 | 2.3e-90 | S | COG NOG27987 non supervised orthologous group | |||
AHJIJCLC_00730 | 4.9e-260 | nhaD | P | Citrate transporter | ||
AHJIJCLC_00731 | 6.9e-103 | Z012_01655 | C | Flavodoxin | ||
AHJIJCLC_00732 | 7.3e-95 | C | Flavodoxin | |||
AHJIJCLC_00733 | 3.4e-173 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
AHJIJCLC_00734 | 1.1e-174 | S | X-Pro dipeptidyl-peptidase (S15 family) | |||
AHJIJCLC_00735 | 1.7e-66 | chbR | K | Transcriptional regulator | ||
AHJIJCLC_00736 | 3.2e-148 | K | helix_turn_helix, arabinose operon control protein | |||
AHJIJCLC_00737 | 6.9e-23 | S | Psort location CytoplasmicMembrane, score | |||
AHJIJCLC_00738 | 4.6e-87 | T | Psort location Cytoplasmic, score 8.96 | |||
AHJIJCLC_00739 | 4.4e-125 | K | Helix-turn-helix domain | |||
AHJIJCLC_00740 | 9.2e-150 | akr5f | S | Aldo/keto reductase family | ||
AHJIJCLC_00741 | 2.5e-231 | J | (SAM)-dependent | |||
AHJIJCLC_00742 | 1.8e-204 | atsB | C | Iron-sulfur cluster-binding domain | ||
AHJIJCLC_00743 | 7.6e-80 | |||||
AHJIJCLC_00744 | 2.6e-07 | |||||
AHJIJCLC_00745 | 1.8e-36 | |||||
AHJIJCLC_00746 | 1.6e-32 | |||||
AHJIJCLC_00747 | 4.8e-35 | |||||
AHJIJCLC_00748 | 1.7e-51 | |||||
AHJIJCLC_00749 | 1.2e-14 | |||||
AHJIJCLC_00751 | 4.8e-84 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
AHJIJCLC_00752 | 4.9e-187 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
AHJIJCLC_00753 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AHJIJCLC_00754 | 2.1e-160 | 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 | |
AHJIJCLC_00755 | 5.6e-98 | 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 | |
AHJIJCLC_00756 | 5.3e-147 | tatD | L | hydrolase, TatD family | ||
AHJIJCLC_00757 | 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 | |
AHJIJCLC_00758 | 6.2e-162 | yunF | F | Protein of unknown function DUF72 | ||
AHJIJCLC_00759 | 1.2e-211 | norA | EGP | Major facilitator Superfamily | ||
AHJIJCLC_00760 | 4.4e-129 | cobB | K | SIR2 family | ||
AHJIJCLC_00761 | 7.2e-186 | |||||
AHJIJCLC_00762 | 6.2e-222 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
AHJIJCLC_00763 | 6.6e-173 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHJIJCLC_00764 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
AHJIJCLC_00765 | 4e-204 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AHJIJCLC_00766 | 9.6e-155 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
AHJIJCLC_00768 | 2.1e-140 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
AHJIJCLC_00769 | 5.1e-24 | phaG | GT1 | I | carboxylic ester hydrolase activity | |
AHJIJCLC_00770 | 6e-58 | K | Transcriptional regulator | |||
AHJIJCLC_00771 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
AHJIJCLC_00772 | 5.6e-197 | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | ||
AHJIJCLC_00773 | 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 | ||
AHJIJCLC_00774 | 1.1e-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 | ||
AHJIJCLC_00775 | 1.4e-153 | jag | S | R3H domain protein | ||
AHJIJCLC_00776 | 3.4e-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 | ||
AHJIJCLC_00777 | 1.4e-56 | 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 | |
AHJIJCLC_00778 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
AHJIJCLC_00780 | 5.2e-248 | 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 | ||
AHJIJCLC_00781 | 1.5e-206 | 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 | |
AHJIJCLC_00782 | 2.2e-34 | yaaA | S | S4 domain protein YaaA | ||
AHJIJCLC_00783 | 3.3e-203 | 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 | ||
AHJIJCLC_00784 | 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 | |
AHJIJCLC_00785 | 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 | |
AHJIJCLC_00786 | 5e-232 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
AHJIJCLC_00787 | 4e-121 | pgm7 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
AHJIJCLC_00788 | 1.6e-117 | dedA | S | SNARE associated Golgi protein | ||
AHJIJCLC_00789 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
AHJIJCLC_00790 | 2.5e-161 | EG | EamA-like transporter family | |||
AHJIJCLC_00791 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AHJIJCLC_00792 | 9.1e-133 | IQ | Dehydrogenase reductase | |||
AHJIJCLC_00793 | 1.5e-82 | 2.3.1.128 | K | acetyltransferase | ||
AHJIJCLC_00794 | 2.2e-08 | |||||
AHJIJCLC_00795 | 9.2e-36 | S | Phage tail-collar fibre protein | |||
AHJIJCLC_00796 | 5.8e-47 | |||||
AHJIJCLC_00797 | 3.6e-157 | S | Baseplate J-like protein | |||
AHJIJCLC_00798 | 4.4e-52 | S | methyltransferase activity | |||
AHJIJCLC_00799 | 5.4e-38 | |||||
AHJIJCLC_00800 | 7.1e-109 | |||||
AHJIJCLC_00801 | 4.2e-69 | |||||
AHJIJCLC_00802 | 4.2e-232 | S | TIGRFAM phage tail tape measure protein, TP901 family, core region | |||
AHJIJCLC_00803 | 2.3e-21 | |||||
AHJIJCLC_00804 | 5.5e-43 | |||||
AHJIJCLC_00805 | 2.1e-60 | |||||
AHJIJCLC_00806 | 1.1e-219 | S | Protein of unknown function (DUF2586) | |||
AHJIJCLC_00807 | 4.5e-15 | |||||
AHJIJCLC_00808 | 1.7e-69 | |||||
AHJIJCLC_00809 | 2.4e-65 | S | S | Phage virion morphogenesis family | ||
AHJIJCLC_00810 | 7.2e-56 | S | Protein of unknown function (DUF1320) | |||
AHJIJCLC_00811 | 2.4e-132 | gpT | S | Mu-like prophage major head subunit gpT | ||
AHJIJCLC_00812 | 1.3e-49 | |||||
AHJIJCLC_00813 | 5.9e-130 | S | Mu-like prophage I protein | |||
AHJIJCLC_00814 | 2.6e-108 | S | Phage Mu protein F like protein | |||
AHJIJCLC_00815 | 2.8e-232 | gp29 | S | Protein of unknown function (DUF935) | ||
AHJIJCLC_00816 | 8.1e-305 | S | TIGRFAM Phage | |||
AHJIJCLC_00817 | 4.9e-86 | S | Protein of unknown function (DUF3486) | |||
AHJIJCLC_00818 | 7.2e-42 | |||||
AHJIJCLC_00819 | 1.2e-32 | |||||
AHJIJCLC_00820 | 2.1e-50 | |||||
AHJIJCLC_00821 | 7.6e-33 | S | Mor transcription activator family | |||
AHJIJCLC_00822 | 2.9e-182 | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
AHJIJCLC_00825 | 6.3e-12 | S | SPTR Toxin-antitoxin system, toxin component, RelE family | |||
AHJIJCLC_00826 | 1.4e-51 | S | Protein of unknown function (DUF1018) | |||
AHJIJCLC_00827 | 3.2e-60 | gam | S | bacteriophage Mu Gam like protein | ||
AHJIJCLC_00828 | 2.2e-131 | 3.6.1.3 | S | AAA domain | ||
AHJIJCLC_00829 | 2e-299 | L | Bacteriophage Mu transposase | |||
AHJIJCLC_00830 | 4.3e-22 | K | Helix-turn-helix XRE-family like proteins | |||
AHJIJCLC_00833 | 9e-37 | |||||
AHJIJCLC_00834 | 6.3e-18 | |||||
AHJIJCLC_00835 | 5.9e-16 | K | sequence-specific DNA binding | |||
AHJIJCLC_00837 | 7.5e-103 | 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 | |
AHJIJCLC_00838 | 2.4e-49 | yktA | S | Belongs to the UPF0223 family | ||
AHJIJCLC_00839 | 2.8e-137 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
AHJIJCLC_00840 | 0.0 | typA | T | GTP-binding protein TypA | ||
AHJIJCLC_00841 | 9.9e-214 | ftsW | D | Belongs to the SEDS family | ||
AHJIJCLC_00842 | 1.4e-47 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AHJIJCLC_00843 | 1.3e-99 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
AHJIJCLC_00844 | 9.6e-89 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
AHJIJCLC_00845 | 6.7e-198 | ylbL | T | Belongs to the peptidase S16 family | ||
AHJIJCLC_00846 | 1.3e-90 | comEA | L | Competence protein ComEA | ||
AHJIJCLC_00847 | 3.4e-88 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
AHJIJCLC_00848 | 0.0 | comEC | S | Competence protein ComEC | ||
AHJIJCLC_00849 | 1.8e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
AHJIJCLC_00850 | 2.3e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
AHJIJCLC_00851 | 4.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
AHJIJCLC_00852 | 1e-139 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AHJIJCLC_00853 | 1.4e-161 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
AHJIJCLC_00854 | 3.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
AHJIJCLC_00855 | 7.1e-104 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
AHJIJCLC_00856 | 1.1e-167 | ypmR | E | lipolytic protein G-D-S-L family | ||
AHJIJCLC_00857 | 3.2e-107 | cat | S | Bacterial transferase hexapeptide (six repeats) | ||
AHJIJCLC_00858 | 2.6e-49 | yhbY | J | RNA-binding protein | ||
AHJIJCLC_00859 | 2.6e-216 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AHJIJCLC_00860 | 2.2e-96 | yqeG | S | HAD phosphatase, family IIIA | ||
AHJIJCLC_00861 | 1.6e-25 | yoaK | S | Protein of unknown function (DUF1275) | ||
AHJIJCLC_00862 | 1.9e-19 | yoaK | S | Protein of unknown function (DUF1275) | ||
AHJIJCLC_00863 | 6.6e-57 | 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 | ||
AHJIJCLC_00864 | 1.5e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
AHJIJCLC_00865 | 1.7e-85 | 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 | ||
AHJIJCLC_00866 | 9.6e-172 | dnaI | L | Primosomal protein DnaI | ||
AHJIJCLC_00867 | 6.1e-146 | dnaB | L | replication initiation and membrane attachment | ||
AHJIJCLC_00868 | 6.4e-18 | P | Sodium:sulfate symporter transmembrane region | |||
AHJIJCLC_00869 | 4.8e-31 | P | Sodium:sulfate symporter transmembrane region | |||
AHJIJCLC_00870 | 8.5e-75 | 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 | |
AHJIJCLC_00871 | 5.4e-246 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
AHJIJCLC_00876 | 2.4e-17 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
AHJIJCLC_00878 | 2.4e-42 | |||||
AHJIJCLC_00879 | 3.2e-248 | 3.6.4.12 | L | UvrD-like helicase C-terminal domain | ||
AHJIJCLC_00880 | 3.2e-112 | L | DNA synthesis involved in DNA repair | |||
AHJIJCLC_00881 | 3.3e-154 | S | Fic family | |||
AHJIJCLC_00882 | 1.7e-97 | S | Pfam:DUF3816 | |||
AHJIJCLC_00883 | 3.6e-142 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
AHJIJCLC_00884 | 1.8e-134 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
AHJIJCLC_00885 | 6.5e-162 | EG | EamA-like transporter family | |||
AHJIJCLC_00886 | 6e-246 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
AHJIJCLC_00888 | 7.2e-15 | |||||
AHJIJCLC_00889 | 5.2e-156 | V | ABC transporter, ATP-binding protein | |||
AHJIJCLC_00890 | 7.8e-64 | gntR1 | K | Transcriptional regulator, GntR family | ||
AHJIJCLC_00891 | 2.5e-172 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
AHJIJCLC_00892 | 3.8e-68 | glfT1 | 1.1.1.133 | S | Glycosyltransferase like family 2 | |
AHJIJCLC_00893 | 1.2e-285 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
AHJIJCLC_00894 | 1.5e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
AHJIJCLC_00895 | 2.2e-215 | 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) | |
AHJIJCLC_00896 | 3.6e-254 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
AHJIJCLC_00897 | 4.7e-159 | hrpQ | 4.6.1.1 | T | histone H2A K63-linked ubiquitination | |
AHJIJCLC_00898 | 2e-169 | ponA | V | Beta-lactamase enzyme family | ||
AHJIJCLC_00899 | 3.1e-265 | yjeM | E | Amino Acid | ||
AHJIJCLC_00901 | 6.1e-111 | |||||
AHJIJCLC_00902 | 6.8e-164 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
AHJIJCLC_00903 | 3.2e-164 | K | LysR substrate binding domain | |||
AHJIJCLC_00904 | 8.2e-116 | D | Alpha beta | |||
AHJIJCLC_00905 | 6.2e-190 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AHJIJCLC_00906 | 7.4e-110 | ysdA | CP | transmembrane transport | ||
AHJIJCLC_00907 | 9.1e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AHJIJCLC_00908 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AHJIJCLC_00909 | 2.8e-249 | malT | G | Major Facilitator | ||
AHJIJCLC_00910 | 2e-97 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
AHJIJCLC_00912 | 1.7e-36 | |||||
AHJIJCLC_00914 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AHJIJCLC_00915 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
AHJIJCLC_00916 | 9.8e-56 | yheA | S | Belongs to the UPF0342 family | ||
AHJIJCLC_00917 | 1.3e-179 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AHJIJCLC_00918 | 3.1e-149 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AHJIJCLC_00920 | 1.4e-77 | hit | FG | histidine triad | ||
AHJIJCLC_00921 | 2.3e-133 | ecsA | V | ABC transporter, ATP-binding protein | ||
AHJIJCLC_00922 | 2.3e-204 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AHJIJCLC_00923 | 6.1e-209 | EG | GntP family permease | |||
AHJIJCLC_00924 | 2.5e-228 | 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 | |
AHJIJCLC_00925 | 2.9e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
AHJIJCLC_00926 | 2.2e-307 | 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 | ||
AHJIJCLC_00927 | 4.8e-108 | 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 | ||
AHJIJCLC_00929 | 2.1e-35 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
AHJIJCLC_00930 | 0.0 | rnjB | J | 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 | ||
AHJIJCLC_00931 | 1.2e-163 | S | Tetratricopeptide repeat | |||
AHJIJCLC_00932 | 3.3e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AHJIJCLC_00933 | 5.7e-215 | 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 | ||
AHJIJCLC_00934 | 1.5e-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 | ||
AHJIJCLC_00935 | 2.3e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
AHJIJCLC_00936 | 8.3e-53 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
AHJIJCLC_00938 | 3.3e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHJIJCLC_00939 | 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 | ||
AHJIJCLC_00940 | 6.7e-52 | T | Protein phosphatase 2C | |||
AHJIJCLC_00941 | 1.3e-33 | D | protein involved in cytokinesis, contains TGc (transglutaminase protease-like) domain | |||
AHJIJCLC_00942 | 6.6e-75 | L | ATPase involved in DNA repair | |||
AHJIJCLC_00943 | 4.7e-108 | P | P-loop Domain of unknown function (DUF2791) | |||
AHJIJCLC_00944 | 9.9e-117 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
AHJIJCLC_00945 | 2.5e-235 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
AHJIJCLC_00946 | 4.5e-208 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
AHJIJCLC_00947 | 3.8e-39 | |||||
AHJIJCLC_00948 | 2.4e-154 | M | glycosyl transferase group 1 | |||
AHJIJCLC_00949 | 1.3e-221 | 3.6.4.12 | L | DnaB-like helicase C terminal domain | ||
AHJIJCLC_00950 | 2.1e-97 | xerC | L | Phage integrase, N-terminal SAM-like domain | ||
AHJIJCLC_00951 | 5.3e-99 | D | Cellulose biosynthesis protein BcsQ | |||
AHJIJCLC_00954 | 7.4e-76 | S | Homeodomain-like domain | |||
AHJIJCLC_00956 | 1.6e-36 | |||||
AHJIJCLC_00959 | 7.6e-216 | 2.1.1.72 | L | DNA methylase | ||
AHJIJCLC_00960 | 1.4e-252 | res_1 | 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
AHJIJCLC_00961 | 8.7e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
AHJIJCLC_00962 | 1.6e-121 | lutA | C | Cysteine-rich domain | ||
AHJIJCLC_00963 | 1.1e-244 | lutB | C | 4Fe-4S dicluster domain | ||
AHJIJCLC_00964 | 5.7e-87 | yrjD | S | LUD domain | ||
AHJIJCLC_00965 | 5.3e-43 | UW | LPXTG-motif cell wall anchor domain protein | |||
AHJIJCLC_00966 | 2.6e-62 | UW | LPXTG-motif cell wall anchor domain protein | |||
AHJIJCLC_00967 | 2.7e-25 | yitW | S | Iron-sulfur cluster assembly protein | ||
AHJIJCLC_00968 | 7.1e-92 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AHJIJCLC_00969 | 4.8e-64 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
AHJIJCLC_00972 | 2.3e-45 | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | |||
AHJIJCLC_00973 | 1.9e-150 | nans | 2.5.1.132, 2.5.1.56, 2.5.1.57 | M | Psort location Cytoplasmic, score 8.96 | |
AHJIJCLC_00974 | 4.2e-37 | ykrP | G | Acyltransferase family | ||
AHJIJCLC_00975 | 3e-87 | neuA | 2.5.1.55, 2.7.7.43, 2.7.7.92, 3.1.3.103, 3.1.3.45 | M | 3-deoxy-D-manno-octulosonate 8-phosphate phosphatase, YrbI family | |
AHJIJCLC_00976 | 2.1e-62 | S | Polysaccharide biosynthesis protein | |||
AHJIJCLC_00977 | 2e-116 | L | Belongs to the 'phage' integrase family | |||
AHJIJCLC_00978 | 5.3e-22 | S | Excisionase | |||
AHJIJCLC_00980 | 9.3e-21 | phyR | K | Sigma-70, region 4 | ||
AHJIJCLC_00981 | 1.2e-22 | S | Domain of unknown function (DUF3846) | |||
AHJIJCLC_00982 | 1.9e-44 | ard | S | Antirestriction protein (ArdA) | ||
AHJIJCLC_00986 | 3.5e-136 | phnE1 | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
AHJIJCLC_00987 | 3.3e-125 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
AHJIJCLC_00988 | 4.7e-132 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
AHJIJCLC_00989 | 1.8e-168 | phnD | P | Phosphonate ABC | ||
AHJIJCLC_00990 | 2.9e-12 | |||||
AHJIJCLC_00995 | 5.6e-13 | |||||
AHJIJCLC_00996 | 1.8e-71 | S | Protein of unknown function (DUF1351) | |||
AHJIJCLC_00997 | 1.4e-138 | recT | L | RecT family | ||
AHJIJCLC_00998 | 3.5e-59 | S | May be involved in the transport of PQQ or its precursor to the periplasm | |||
AHJIJCLC_00999 | 5e-53 | S | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_01001 | 5e-37 | L | Single-strand binding protein family | |||
AHJIJCLC_01002 | 3.9e-35 | L | dnaD_dom DnaD domain protein | |||
AHJIJCLC_01003 | 1.8e-309 | ubiB | S | ABC1 family | ||
AHJIJCLC_01004 | 2.3e-130 | 1.14.12.17 | C | Oxidoreductase NAD-binding domain | ||
AHJIJCLC_01005 | 8.8e-170 | GK | ROK family | |||
AHJIJCLC_01006 | 1.1e-40 | |||||
AHJIJCLC_01007 | 4.2e-80 | copY | K | Copper transport repressor CopY TcrY | ||
AHJIJCLC_01009 | 1.1e-169 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
AHJIJCLC_01010 | 2e-310 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | carbohydrate kinase FGGY | |
AHJIJCLC_01011 | 1.4e-138 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
AHJIJCLC_01012 | 5.8e-205 | araR | K | Transcriptional regulator | ||
AHJIJCLC_01013 | 1.3e-201 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AHJIJCLC_01014 | 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 | ||
AHJIJCLC_01015 | 6.5e-96 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
AHJIJCLC_01016 | 1.2e-128 | comFC | S | Competence protein | ||
AHJIJCLC_01017 | 5.9e-252 | comFA | L | Helicase C-terminal domain protein | ||
AHJIJCLC_01018 | 1.1e-113 | yvyE | 3.4.13.9 | S | YigZ family | |
AHJIJCLC_01019 | 6.4e-38 | |||||
AHJIJCLC_01020 | 2.4e-256 | ydaO | E | amino acid | ||
AHJIJCLC_01021 | 1.7e-131 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AHJIJCLC_01022 | 6e-154 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
AHJIJCLC_01023 | 2.6e-169 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
AHJIJCLC_01024 | 3.8e-198 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
AHJIJCLC_01025 | 1.6e-171 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHJIJCLC_01026 | 2.8e-137 | cof | S | haloacid dehalogenase-like hydrolase | ||
AHJIJCLC_01027 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AHJIJCLC_01028 | 6.8e-113 | yfbR | S | HD containing hydrolase-like enzyme | ||
AHJIJCLC_01030 | 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 | ||
AHJIJCLC_01031 | 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 | ||
AHJIJCLC_01032 | 7.6e-205 | |||||
AHJIJCLC_01033 | 3.3e-158 | rapZ | S | Displays ATPase and GTPase activities | ||
AHJIJCLC_01034 | 1.7e-187 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
AHJIJCLC_01035 | 1.9e-167 | whiA | K | May be required for sporulation | ||
AHJIJCLC_01036 | 2.5e-118 | 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 | |
AHJIJCLC_01037 | 1.3e-102 | clpP | 3.4.21.92 | O | 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 | |
AHJIJCLC_01041 | 2.2e-96 | V | VanZ like family | |||
AHJIJCLC_01042 | 1.1e-220 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
AHJIJCLC_01043 | 2.5e-61 | yneR | ||||
AHJIJCLC_01044 | 1.9e-181 | K | Transcriptional regulator, LacI family | |||
AHJIJCLC_01045 | 3.2e-229 | gntT | EG | Gluconate | ||
AHJIJCLC_01046 | 2.2e-287 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
AHJIJCLC_01047 | 8.3e-108 | mutR | K | Transcriptional activator, Rgg GadR MutR family | ||
AHJIJCLC_01048 | 8.7e-51 | mutR | K | Transcriptional activator, Rgg GadR MutR family | ||
AHJIJCLC_01050 | 1.7e-119 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AHJIJCLC_01052 | 2.2e-199 | gldA | 1.1.1.6 | C | dehydrogenase | |
AHJIJCLC_01053 | 1.3e-16 | xre | K | Helix-turn-helix domain | ||
AHJIJCLC_01054 | 2e-51 | S | Sugar efflux transporter for intercellular exchange | |||
AHJIJCLC_01055 | 3e-56 | 1.14.99.57 | S | Antibiotic biosynthesis monooxygenase | ||
AHJIJCLC_01056 | 8.7e-44 | S | Protein conserved in bacteria | |||
AHJIJCLC_01057 | 3.3e-112 | L | Psort location Cytoplasmic, score 8.96 | |||
AHJIJCLC_01058 | 0.0 | |||||
AHJIJCLC_01059 | 3.1e-237 | |||||
AHJIJCLC_01061 | 2.2e-190 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
AHJIJCLC_01062 | 4.1e-90 | M | Glycosyl transferase family 2 | |||
AHJIJCLC_01063 | 1.6e-54 | gspA | M | Psort location Cytoplasmic, score 8.96 | ||
AHJIJCLC_01064 | 2e-66 | M | Glycosyl transferases group 1 | |||
AHJIJCLC_01065 | 1.2e-90 | GT2,GT4 | M | Glycosyltransferase like family 2 | ||
AHJIJCLC_01066 | 5.8e-65 | gspA | M | Psort location Cytoplasmic, score 8.96 | ||
AHJIJCLC_01067 | 2.9e-83 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
AHJIJCLC_01068 | 8.1e-81 | 2.7.8.12 | GT2 | M | Glycosyltransferase like family 2 | |
AHJIJCLC_01069 | 1.5e-191 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
AHJIJCLC_01070 | 2.7e-101 | 3.2.1.40 | G | Alpha-L-rhamnosidase | ||
AHJIJCLC_01071 | 8.5e-49 | nlhH_1 | I | Carboxylesterase family | ||
AHJIJCLC_01072 | 3.6e-108 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
AHJIJCLC_01073 | 0.0 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AHJIJCLC_01074 | 1.1e-86 | adhA | 1.1.1.1 | C | Zinc-binding alcohol dehydrogenase family protein | |
AHJIJCLC_01075 | 3e-227 | ktrB | P | Potassium uptake protein | ||
AHJIJCLC_01076 | 3.3e-197 | 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 | |
AHJIJCLC_01077 | 6.5e-218 | patA | 2.6.1.1 | E | Aminotransferase | |
AHJIJCLC_01078 | 2.8e-140 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
AHJIJCLC_01079 | 1.3e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AHJIJCLC_01080 | 3.3e-118 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AHJIJCLC_01081 | 1.5e-118 | S | Protein of unknown function (DUF554) | |||
AHJIJCLC_01082 | 9e-256 | rarA | L | recombination factor protein RarA | ||
AHJIJCLC_01084 | 0.0 | oppD | EP | Psort location Cytoplasmic, score | ||
AHJIJCLC_01085 | 8e-243 | codA | 3.5.4.1 | F | cytosine deaminase | |
AHJIJCLC_01086 | 1.6e-244 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
AHJIJCLC_01087 | 1e-82 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
AHJIJCLC_01088 | 0.0 | icmB | U | type IV secretory pathway VirB4 | ||
AHJIJCLC_01089 | 1.5e-201 | |||||
AHJIJCLC_01090 | 2.9e-25 | |||||
AHJIJCLC_01091 | 0.0 | |||||
AHJIJCLC_01092 | 1.3e-100 | |||||
AHJIJCLC_01093 | 4.1e-127 | larA | 5.1.2.1 | S | Domain of unknown function (DUF2088) | |
AHJIJCLC_01094 | 1.7e-131 | cpmA | S | AIR carboxylase | ||
AHJIJCLC_01095 | 2.4e-216 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
AHJIJCLC_01096 | 4.5e-129 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AHJIJCLC_01097 | 1.7e-148 | larE | S | NAD synthase | ||
AHJIJCLC_01098 | 5.3e-184 | hoxN | U | High-affinity nickel-transport protein | ||
AHJIJCLC_01099 | 0.0 | GT2,GT4 | M | PFAM Glycosyl transferase family 2 | ||
AHJIJCLC_01100 | 2.7e-53 | H | Methyltransferase domain | |||
AHJIJCLC_01101 | 1.1e-74 | H | Methyltransferase domain | |||
AHJIJCLC_01102 | 1.4e-143 | 2.7.8.14, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | ||
AHJIJCLC_01103 | 7.7e-97 | ispD | 2.7.7.60, 4.6.1.12 | I | 2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase | |
AHJIJCLC_01104 | 2.4e-139 | GM | 3-beta hydroxysteroid dehydrogenase/isomerase family | |||
AHJIJCLC_01105 | 3.3e-84 | M | Glycosyltransferase like family 2 | |||
AHJIJCLC_01106 | 5.1e-180 | S | Terminase-like family | |||
AHJIJCLC_01107 | 9.6e-21 | xtmA | L | Homeodomain-like domain | ||
AHJIJCLC_01110 | 7.2e-53 | traI | S | metal-dependent phosphohydrolase, HD sub domain | ||
AHJIJCLC_01116 | 2.3e-74 | dcm | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | |
AHJIJCLC_01117 | 3.7e-140 | pstA | P | Phosphate transport system permease protein PstA | ||
AHJIJCLC_01118 | 2.6e-135 | 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 | |
AHJIJCLC_01119 | 1.1e-122 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AHJIJCLC_01120 | 2.9e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
AHJIJCLC_01121 | 2e-39 | ylqC | S | Belongs to the UPF0109 family | ||
AHJIJCLC_01122 | 2.1e-88 | 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 | ||
AHJIJCLC_01123 | 1.2e-140 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AHJIJCLC_01124 | 7.5e-261 | yfnA | E | Amino Acid | ||
AHJIJCLC_01126 | 1.4e-33 | feoA | P | FeoA domain | ||
AHJIJCLC_01127 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
AHJIJCLC_01128 | 6.7e-23 | S | Virus attachment protein p12 family | |||
AHJIJCLC_01129 | 2.4e-156 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
AHJIJCLC_01130 | 5.5e-178 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AHJIJCLC_01131 | 2.5e-183 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
AHJIJCLC_01132 | 7.2e-158 | aspB | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
AHJIJCLC_01133 | 7.2e-83 | lytH | 3.5.1.28 | M | Ami_3 | |
AHJIJCLC_01134 | 2.5e-64 | yniA | G | Phosphotransferase enzyme family | ||
AHJIJCLC_01135 | 1.3e-62 | yniA | G | Phosphotransferase enzyme family | ||
AHJIJCLC_01136 | 1.1e-172 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AHJIJCLC_01137 | 1.2e-245 | mmuP | E | amino acid | ||
AHJIJCLC_01138 | 2e-157 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
AHJIJCLC_01139 | 8.1e-213 | hom1 | 1.1.1.3 | E | Homoserine dehydrogenase | |
AHJIJCLC_01141 | 2.7e-137 | IQ | KR domain | |||
AHJIJCLC_01142 | 2.5e-98 | K | DNA-templated transcription, initiation | |||
AHJIJCLC_01143 | 7.1e-74 | IQ | reductase | |||
AHJIJCLC_01144 | 4e-241 | treB | G | phosphotransferase system | ||
AHJIJCLC_01145 | 2.1e-70 | treR | K | UTRA | ||
AHJIJCLC_01146 | 2.7e-238 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AHJIJCLC_01148 | 4.7e-26 | |||||
AHJIJCLC_01149 | 1.1e-27 | L | Toxic component of a toxin-antitoxin (TA) module | |||
AHJIJCLC_01152 | 1.4e-124 | 2.7.7.19 | S | Psort location Cytoplasmic, score | ||
AHJIJCLC_01153 | 2.3e-130 | L | RAMP superfamily | |||
AHJIJCLC_01154 | 1.6e-89 | L | RAMP superfamily | |||
AHJIJCLC_01155 | 4.8e-07 | |||||
AHJIJCLC_01156 | 2.3e-119 | L | RAMP superfamily | |||
AHJIJCLC_01157 | 4.1e-46 | S | CRISPR-associated (Cas) DxTHG family | |||
AHJIJCLC_01158 | 1.8e-41 | S | CRISPR-associated (Cas) DxTHG family | |||
AHJIJCLC_01159 | 1.6e-06 | |||||
AHJIJCLC_01160 | 6.3e-46 | cas6 | S | CRISPR-associated endoribonuclease Cas6 | ||
AHJIJCLC_01161 | 1.7e-47 | O | S-layer homology domain | |||
AHJIJCLC_01162 | 2.9e-263 | arcD | E | Amino acid permease | ||
AHJIJCLC_01163 | 2.9e-198 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
AHJIJCLC_01164 | 1.6e-106 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHJIJCLC_01165 | 6.2e-77 | yncA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
AHJIJCLC_01166 | 3.7e-85 | S | Fic/DOC family | |||
AHJIJCLC_01167 | 2.5e-95 | apt | 2.4.2.22, 2.4.2.7 | F | Phosphoribosyl transferase domain | |
AHJIJCLC_01168 | 2.9e-246 | EGP | Sugar (and other) transporter | |||
AHJIJCLC_01169 | 5.6e-184 | 1.4.1.1, 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | ||
AHJIJCLC_01170 | 7.7e-216 | 2.6.1.1 | E | Aminotransferase | ||
AHJIJCLC_01173 | 3e-61 | xkdG | S | Phage capsid family | ||
AHJIJCLC_01174 | 3.5e-39 | S | Caudovirus prohead serine protease | |||
AHJIJCLC_01175 | 2e-158 | S | Phage portal protein | |||
AHJIJCLC_01176 | 1.4e-167 | S | Terminase | |||
AHJIJCLC_01178 | 3.9e-18 | L | HNH nucleases | |||
AHJIJCLC_01181 | 2.3e-16 | S | Protein of unknwon function (DUF3310) | |||
AHJIJCLC_01182 | 4.8e-19 | |||||
AHJIJCLC_01189 | 5.2e-86 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
AHJIJCLC_01191 | 7e-11 | S | Phage uncharacterised protein (Phage_XkdX) | |||
AHJIJCLC_01192 | 1.3e-19 | |||||
AHJIJCLC_01193 | 5.4e-28 | |||||
AHJIJCLC_01194 | 1.6e-26 | |||||
AHJIJCLC_01195 | 4.7e-45 | |||||
AHJIJCLC_01197 | 4.1e-123 | |||||
AHJIJCLC_01198 | 3.4e-51 | |||||
AHJIJCLC_01199 | 3.3e-09 | |||||
AHJIJCLC_01200 | 1.9e-112 | 3.1.3.73 | G | phosphoglycerate mutase | ||
AHJIJCLC_01201 | 7.5e-18 | C | aldo keto reductase | |||
AHJIJCLC_01202 | 1.2e-80 | C | aldo keto reductase | |||
AHJIJCLC_01203 | 1.3e-201 | 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 | |
AHJIJCLC_01204 | 4.8e-221 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHJIJCLC_01205 | 2.2e-102 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
AHJIJCLC_01206 | 2.4e-226 | 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 | |
AHJIJCLC_01207 | 4.9e-108 | 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 | |
AHJIJCLC_01208 | 7.1e-217 | 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 | |
AHJIJCLC_01209 | 1.5e-168 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
AHJIJCLC_01210 | 6.5e-51 | hisF | 3.5.4.19, 3.6.1.31 | 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 | |
AHJIJCLC_01211 | 1.6e-08 | hisF | 3.5.4.19, 3.6.1.31 | 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 | |
AHJIJCLC_01212 | 2.4e-53 | 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 | ||
AHJIJCLC_01213 | 0.0 | S | PglZ domain | |||
AHJIJCLC_01214 | 0.0 | 3.4.21.53 | O | Putative ATP-dependent Lon protease | ||
AHJIJCLC_01215 | 0.0 | yfjM | S | Protein of unknown function DUF262 | ||
AHJIJCLC_01216 | 6.1e-08 | D | Transglutaminase-like domain | |||
AHJIJCLC_01217 | 1.9e-47 | O | Heat shock 70 kDa protein | |||
AHJIJCLC_01220 | 6.2e-45 | sulP | P | Psort location CytoplasmicMembrane, score 9.99 | ||
AHJIJCLC_01221 | 2.5e-25 | |||||
AHJIJCLC_01222 | 7.4e-22 | S | Rhomboid family | |||
AHJIJCLC_01223 | 1.2e-256 | gp17a | S | Mu-like prophage FluMu protein gp28 | ||
AHJIJCLC_01225 | 5.2e-238 | |||||
AHJIJCLC_01226 | 4.5e-78 | mutS | L | Helicase C-terminal domain protein | ||
AHJIJCLC_01227 | 3.5e-16 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
AHJIJCLC_01228 | 1.7e-69 | 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 | |
AHJIJCLC_01229 | 4.5e-113 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
AHJIJCLC_01230 | 9.4e-205 | coiA | 3.6.4.12 | S | Competence protein | |
AHJIJCLC_01231 | 2.6e-112 | yjbH | Q | Thioredoxin | ||
AHJIJCLC_01232 | 6e-123 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
AHJIJCLC_01233 | 1.3e-153 | 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 | |
AHJIJCLC_01234 | 8.2e-173 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
AHJIJCLC_01235 | 1.4e-195 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
AHJIJCLC_01236 | 9.7e-163 | rrmA | 2.1.1.187 | H | Methyltransferase | |
AHJIJCLC_01237 | 6.7e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
AHJIJCLC_01238 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
AHJIJCLC_01239 | 1.2e-07 | S | Protein of unknown function (DUF4044) | |||
AHJIJCLC_01240 | 5.8e-58 | |||||
AHJIJCLC_01241 | 5.6e-79 | mraZ | K | Belongs to the MraZ family | ||
AHJIJCLC_01242 | 2.5e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AHJIJCLC_01243 | 7e-09 | ftsL | D | Cell division protein FtsL | ||
AHJIJCLC_01244 | 1.2e-79 | V | Psort location CytoplasmicMembrane, score 9.99 | |||
AHJIJCLC_01245 | 6.2e-120 | 3.4.17.11 | E | Peptidase family M28 | ||
AHJIJCLC_01246 | 2.5e-75 | K | Transcriptional regulator | |||
AHJIJCLC_01247 | 1.4e-11 | |||||
AHJIJCLC_01248 | 9.3e-111 | S | Calcineurin-like phosphoesterase | |||
AHJIJCLC_01249 | 1.1e-42 | E | Peptidase dimerisation domain | |||
AHJIJCLC_01250 | 1.6e-11 | yhaA1 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | ||
AHJIJCLC_01251 | 2.3e-14 | pilD | 3.4.23.43 | NOU | aspartic-type endopeptidase activity | |
AHJIJCLC_01252 | 2.2e-213 | ykiI | ||||
AHJIJCLC_01253 | 2.5e-135 | puuD | S | peptidase C26 | ||
AHJIJCLC_01254 | 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 | |
AHJIJCLC_01255 | 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 | |
AHJIJCLC_01256 | 5.8e-106 | K | Bacterial regulatory proteins, tetR family | |||
AHJIJCLC_01257 | 0.0 | clpC | 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 | ||
AHJIJCLC_01258 | 4.8e-79 | ctsR | K | Belongs to the CtsR family | ||
AHJIJCLC_01259 | 9.7e-194 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
AHJIJCLC_01260 | 3.2e-95 | K | transcriptional regulator | |||
AHJIJCLC_01261 | 2.2e-72 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
AHJIJCLC_01262 | 0.0 | L | Helicase C-terminal domain protein | |||
AHJIJCLC_01263 | 1.6e-54 | S | MazG-like family | |||
AHJIJCLC_01264 | 4.7e-108 | lssY | 3.6.1.27 | I | Acid phosphatase homologues | |
AHJIJCLC_01265 | 1.2e-199 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
AHJIJCLC_01266 | 2e-97 | |||||
AHJIJCLC_01267 | 2.9e-224 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AHJIJCLC_01268 | 1.9e-118 | ponA | V | Beta-lactamase enzyme family | ||
AHJIJCLC_01269 | 3.3e-58 | ytzB | S | Small secreted protein | ||
AHJIJCLC_01270 | 6.5e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
AHJIJCLC_01271 | 2e-117 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHJIJCLC_01272 | 4.2e-250 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AHJIJCLC_01273 | 1.8e-114 | ybhL | S | Belongs to the BI1 family | ||
AHJIJCLC_01274 | 1.5e-138 | aroD | S | Serine hydrolase (FSH1) | ||
AHJIJCLC_01279 | 6e-289 | L | SNF2 family N-terminal domain | |||
AHJIJCLC_01280 | 1.2e-51 | |||||
AHJIJCLC_01281 | 6.2e-70 | |||||
AHJIJCLC_01282 | 6e-70 | S | Psort location Cytoplasmic, score 8.96 | |||
AHJIJCLC_01283 | 5.5e-79 | S | Erf family | |||
AHJIJCLC_01285 | 4.7e-16 | |||||
AHJIJCLC_01286 | 6.5e-55 | K | helix_turn_helix, Lux Regulon | |||
AHJIJCLC_01289 | 2.1e-42 | |||||
AHJIJCLC_01291 | 1.8e-38 | K | Transcriptional regulator | |||
AHJIJCLC_01299 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AHJIJCLC_01300 | 1.1e-197 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AHJIJCLC_01301 | 7.8e-60 | yodB | K | Transcriptional regulator, HxlR family | ||
AHJIJCLC_01302 | 7.8e-91 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
AHJIJCLC_01303 | 1.2e-141 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AHJIJCLC_01304 | 4.1e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
AHJIJCLC_01305 | 8.8e-184 | |||||
AHJIJCLC_01306 | 1.2e-39 | |||||
AHJIJCLC_01307 | 4e-116 | nreC | K | PFAM regulatory protein LuxR | ||
AHJIJCLC_01308 | 1.6e-183 | comP | 2.7.13.3 | F | Sensor histidine kinase | |
AHJIJCLC_01309 | 1.4e-77 | nreA | T | GAF domain | ||
AHJIJCLC_01310 | 4.2e-40 | |||||
AHJIJCLC_01311 | 1.5e-97 | 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 | |
AHJIJCLC_01312 | 9.3e-85 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
AHJIJCLC_01313 | 5.3e-49 | moeA | 2.10.1.1 | H | MoeA N-terminal region (domain I and II) | |
AHJIJCLC_01314 | 1.6e-53 | yhdP | S | Transporter associated domain | ||
AHJIJCLC_01315 | 1.5e-89 | GM | epimerase | |||
AHJIJCLC_01316 | 1.3e-85 | M1-874 | K | Domain of unknown function (DUF1836) | ||
AHJIJCLC_01317 | 9.8e-157 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
AHJIJCLC_01318 | 1.7e-265 | pipD | E | Dipeptidase | ||
AHJIJCLC_01319 | 3.2e-130 | |||||
AHJIJCLC_01320 | 7.1e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AHJIJCLC_01321 | 6.4e-131 | gntR | K | UbiC transcription regulator-associated domain protein | ||
AHJIJCLC_01322 | 7.5e-64 | rumA | 2.1.1.190 | H | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AHJIJCLC_01323 | 6e-150 | 2.1.1.72, 3.1.21.3 | L | Type I restriction modification DNA specificity domain | ||
AHJIJCLC_01324 | 2e-07 | |||||
AHJIJCLC_01325 | 0.0 | draG | 2.1.1.72 | V | Overlaps another CDS with the same product name | |
AHJIJCLC_01326 | 1.7e-199 | 2.1.1.72 | V | Overlaps another CDS with the same product name | ||
AHJIJCLC_01327 | 1.5e-113 | 2.1.1.72, 3.1.21.3 | L | Type I restriction modification DNA specificity domain | ||
AHJIJCLC_01328 | 0.0 | hsdR | 3.1.21.3 | L | Type I restriction enzyme R protein N terminus (HSDR_N) | |
AHJIJCLC_01329 | 3.8e-16 | |||||
AHJIJCLC_01330 | 3e-143 | E | Zn peptidase | |||
AHJIJCLC_01331 | 1.8e-58 | K | DNA-templated transcription, initiation | |||
AHJIJCLC_01332 | 6e-53 | S | Psort location Cytoplasmic, score | |||
AHJIJCLC_01333 | 8e-90 | |||||
AHJIJCLC_01334 | 0.0 | L | Virulence-associated protein E | |||
AHJIJCLC_01335 | 1.1e-33 | S | VRR-NUC domain protein | |||
AHJIJCLC_01336 | 2.8e-217 | L | snf2 family | |||
AHJIJCLC_01337 | 4.3e-22 | |||||
AHJIJCLC_01338 | 3.1e-53 | K | Protein of unknown function (DUF1492) | |||
AHJIJCLC_01340 | 2.1e-46 | L | HNH endonuclease | |||
AHJIJCLC_01341 | 1.2e-91 | |||||
AHJIJCLC_01342 | 3.9e-34 | |||||
AHJIJCLC_01343 | 3.8e-232 | 2.1.1.72 | KL | ParB-like nuclease domain | ||
AHJIJCLC_01344 | 1.1e-99 | S | Psort location Cytoplasmic, score | |||
AHJIJCLC_01345 | 3.5e-32 | S | Domain of unknown function (DUF4314) | |||
AHJIJCLC_01346 | 0.0 | M | COG COG3209 Rhs family protein | |||
AHJIJCLC_01348 | 0.0 | M | COG3209 Rhs family protein | |||
AHJIJCLC_01350 | 2e-35 | S | Psort location Cytoplasmic, score 8.96 | |||
AHJIJCLC_01351 | 1.4e-64 | M1-568 | M | Collagen binding domain | ||
AHJIJCLC_01352 | 1.2e-63 | repB | L | Initiator Replication protein | ||
AHJIJCLC_01353 | 2.9e-162 | F | DNA/RNA non-specific endonuclease | |||
AHJIJCLC_01354 | 1.2e-69 | L | nuclease | |||
AHJIJCLC_01355 | 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) | |
AHJIJCLC_01356 | 6.4e-22 | |||||
AHJIJCLC_01357 | 9.7e-278 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AHJIJCLC_01358 | 7.1e-189 | tdh | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
AHJIJCLC_01359 | 3.7e-108 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
AHJIJCLC_01360 | 6e-159 | hrtB | V | ABC transporter permease | ||
AHJIJCLC_01361 | 5.5e-124 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
AHJIJCLC_01362 | 1.8e-75 | argR | K | Regulates arginine biosynthesis genes | ||
AHJIJCLC_01363 | 2.6e-46 | czrA | K | Transcriptional regulator, ArsR family | ||
AHJIJCLC_01364 | 2.7e-174 | acm2 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |
AHJIJCLC_01365 | 2e-169 | scrR | K | Transcriptional regulator, LacI family | ||
AHJIJCLC_01366 | 9.5e-26 | |||||
AHJIJCLC_01367 | 4.1e-102 | |||||
AHJIJCLC_01368 | 1e-96 | 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 | ||
AHJIJCLC_01369 | 8.5e-108 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the epimerization of the S- and R-forms of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration. This is a prerequisite for the S- specific NAD(P)H-hydrate dehydratase to allow the repair of both epimers of NAD(P)HX | |
AHJIJCLC_01370 | 5.6e-55 | |||||
AHJIJCLC_01371 | 4.8e-125 | yrkL | S | Flavodoxin-like fold | ||
AHJIJCLC_01373 | 6.8e-65 | yeaO | S | Protein of unknown function, DUF488 | ||
AHJIJCLC_01374 | 1.3e-116 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
AHJIJCLC_01375 | 9.5e-206 | 3.1.3.1 | S | associated with various cellular activities | ||
AHJIJCLC_01376 | 1.5e-214 | S | Putative metallopeptidase domain | |||
AHJIJCLC_01377 | 2.5e-46 | |||||
AHJIJCLC_01378 | 1.8e-229 | pbuG | S | permease | ||
AHJIJCLC_01379 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AHJIJCLC_01380 | 1.1e-92 | ymdB | S | Macro domain protein | ||
AHJIJCLC_01381 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AHJIJCLC_01382 | 1.1e-92 | ymdB | S | Macro domain protein | ||
AHJIJCLC_01383 | 6.9e-147 | pnuC | H | nicotinamide mononucleotide transporter | ||
AHJIJCLC_01384 | 7.6e-80 | 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 | ||
AHJIJCLC_01385 | 1.4e-170 | MA20_03535 | 1.1.1.399, 1.1.1.95 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AHJIJCLC_01386 | 2e-52 | |||||
AHJIJCLC_01387 | 5.7e-141 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
AHJIJCLC_01388 | 5.3e-119 | tcyB | U | Binding-protein-dependent transport system inner membrane component | ||
AHJIJCLC_01389 | 6.6e-136 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AHJIJCLC_01390 | 6.9e-36 | |||||
AHJIJCLC_01391 | 2.7e-96 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
AHJIJCLC_01392 | 7e-139 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AHJIJCLC_01393 | 1.2e-182 | celE | 3.2.1.4 | GH5,GH9 | E | GDSL-like Lipase/Acylhydrolase family |
AHJIJCLC_01394 | 3e-223 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AHJIJCLC_01395 | 4e-286 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AHJIJCLC_01396 | 5.1e-179 | galR | K | Transcriptional regulator | ||
AHJIJCLC_01397 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
AHJIJCLC_01398 | 6.6e-276 | lacS | G | Transporter | ||
AHJIJCLC_01399 | 1.6e-21 | 3.6.1.67 | L | COG COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
AHJIJCLC_01400 | 3e-280 | 1.8.4.10, 1.8.4.8 | CEH | Phosphoadenosine phosphosulfate reductase family | ||
AHJIJCLC_01401 | 5.2e-111 | S | Protein of unknown function (DUF4007) | |||
AHJIJCLC_01402 | 0.0 | P | ATPase activity | |||
AHJIJCLC_01403 | 7.4e-142 | sufS | 2.8.1.7, 4.4.1.16 | E | TIGRFAM cysteine desulfurase family protein | |
AHJIJCLC_01404 | 5.6e-284 | L | helicase superfamily c-terminal domain | |||
AHJIJCLC_01406 | 2.8e-229 | L | AAA domain | |||
AHJIJCLC_01407 | 2e-68 | |||||
AHJIJCLC_01408 | 6.9e-255 | 2.7.7.7 | K | Bacterial RNA polymerase, alpha chain C terminal domain | ||
AHJIJCLC_01409 | 1.6e-180 | S | PD-(D/E)XK nuclease superfamily | |||
AHJIJCLC_01410 | 2.2e-25 | S | PD-(D/E)XK nuclease superfamily | |||
AHJIJCLC_01411 | 7.3e-61 | S | KAP family P-loop domain | |||
AHJIJCLC_01412 | 3.2e-52 | rfbC | 5.1.3.13 | M | 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 | |
AHJIJCLC_01413 | 3.2e-46 | 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 | |
AHJIJCLC_01414 | 3.9e-113 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
AHJIJCLC_01415 | 3.3e-15 | |||||
AHJIJCLC_01416 | 2.4e-306 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AHJIJCLC_01417 | 6.2e-76 | argR | K | Regulates arginine biosynthesis genes | ||
AHJIJCLC_01418 | 3.2e-147 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AHJIJCLC_01419 | 9.6e-158 | 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 | |
AHJIJCLC_01420 | 1e-18 | 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 | |
AHJIJCLC_01421 | 8.3e-35 | 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 | |
AHJIJCLC_01424 | 1.4e-29 | L | HNH nucleases | |||
AHJIJCLC_01425 | 4.6e-38 | |||||
AHJIJCLC_01426 | 7.1e-226 | S | Terminase | |||
AHJIJCLC_01427 | 5.8e-95 | S | Phage portal protein | |||
AHJIJCLC_01429 | 3.1e-97 | S | Phage major capsid protein, HK97 family | |||
AHJIJCLC_01431 | 2.4e-15 | S | Phage gp6-like head-tail connector protein | |||
AHJIJCLC_01432 | 3.3e-26 | S | head-tail adaptor | |||
AHJIJCLC_01433 | 1.3e-16 | S | Psort location Cytoplasmic, score | |||
AHJIJCLC_01434 | 9.7e-20 | |||||
AHJIJCLC_01435 | 2.8e-40 | S | phage major tail protein, phi13 family | |||
AHJIJCLC_01436 | 7e-28 | S | Psort location Cytoplasmic, score 7.50 | |||
AHJIJCLC_01437 | 6.1e-108 | nlpD | M | Phage-related minor tail protein | ||
AHJIJCLC_01438 | 1.2e-154 | K | Appr-1'-p processing enzyme | |||
AHJIJCLC_01439 | 1.7e-86 | XK26_04895 | ||||
AHJIJCLC_01440 | 2e-33 | |||||
AHJIJCLC_01442 | 2.3e-61 | |||||
AHJIJCLC_01443 | 7.2e-142 | mnaA | 5.1.3.14 | M | UDP-N-acetylglucosamine 2-epimerase | |
AHJIJCLC_01444 | 1.3e-122 | G | Glycosyl hydrolases family 8 | |||
AHJIJCLC_01445 | 2.5e-186 | ydaM | M | Glycosyl transferase family group 2 | ||
AHJIJCLC_01447 | 1.1e-78 | |||||
AHJIJCLC_01448 | 1.3e-137 | V | domain protein | |||
AHJIJCLC_01449 | 2.1e-183 | fecB | P | Periplasmic binding protein | ||
AHJIJCLC_01450 | 7.2e-272 | sufB | O | assembly protein SufB | ||
AHJIJCLC_01451 | 3.2e-83 | nifU | C | SUF system FeS assembly protein, NifU family | ||
AHJIJCLC_01452 | 5.8e-233 | 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 | |
AHJIJCLC_01453 | 1.3e-243 | sufD | O | FeS assembly protein SufD | ||
AHJIJCLC_01454 | 9.4e-144 | sufC | O | FeS assembly ATPase SufC | ||
AHJIJCLC_01455 | 4.7e-123 | srtA | 3.4.22.70 | M | sortase family | |
AHJIJCLC_01456 | 4.8e-47 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AHJIJCLC_01457 | 8.7e-88 | lemA | S | LemA family | ||
AHJIJCLC_01458 | 4.9e-157 | htpX | O | Belongs to the peptidase M48B family | ||
AHJIJCLC_01459 | 2.1e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
AHJIJCLC_01460 | 6.6e-252 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
AHJIJCLC_01461 | 2.9e-60 | 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 | |
AHJIJCLC_01462 | 9.6e-211 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AHJIJCLC_01463 | 5e-57 | L | Toxic component of a toxin-antitoxin (TA) module | |||
AHJIJCLC_01464 | 8.1e-114 | S | (CBS) domain | |||
AHJIJCLC_01465 | 8.2e-102 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
AHJIJCLC_01466 | 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 | ||
AHJIJCLC_01467 | 1.6e-39 | yabO | J | S4 domain protein | ||
AHJIJCLC_01468 | 1.5e-56 | divIC | D | Septum formation initiator | ||
AHJIJCLC_01469 | 3e-87 | yabR | J | RNA binding | ||
AHJIJCLC_01470 | 2.8e-257 | tilS | 2.4.2.8, 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 | |
AHJIJCLC_01471 | 4.1e-98 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AHJIJCLC_01472 | 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 | ||
AHJIJCLC_01473 | 1.3e-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 | ||
AHJIJCLC_01474 | 5.4e-189 | 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 | ||
AHJIJCLC_01475 | 1.2e-290 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AHJIJCLC_01476 | 1.2e-21 | 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 | |
AHJIJCLC_01477 | 2e-247 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
AHJIJCLC_01478 | 1.4e-130 | stp | 3.1.3.16 | T | phosphatase | |
AHJIJCLC_01479 | 0.0 | KLT | serine threonine protein kinase | |||
AHJIJCLC_01480 | 4.1e-164 | 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 | |
AHJIJCLC_01481 | 1.1e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AHJIJCLC_01482 | 4.4e-246 | S | response to antibiotic | |||
AHJIJCLC_01483 | 1.9e-135 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
AHJIJCLC_01484 | 3e-37 | 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 | |
AHJIJCLC_01485 | 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 | |
AHJIJCLC_01486 | 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 | |
AHJIJCLC_01487 | 5.7e-280 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
AHJIJCLC_01488 | 2e-194 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
AHJIJCLC_01489 | 6e-108 | 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 | |
AHJIJCLC_01490 | 1.6e-140 | fhuC | 3.6.3.34 | HP | ABC transporter, ATP-binding protein | |
AHJIJCLC_01491 | 7.5e-153 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AHJIJCLC_01492 | 2.8e-149 | isdE | P | Periplasmic binding protein | ||
AHJIJCLC_01493 | 1e-94 | M | Iron Transport-associated domain | |||
AHJIJCLC_01494 | 3.8e-265 | isdH | M | Iron Transport-associated domain | ||
AHJIJCLC_01495 | 1.4e-93 | 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 | ||
AHJIJCLC_01496 | 1.6e-129 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
AHJIJCLC_01497 | 3.2e-153 | 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 | ||
AHJIJCLC_01498 | 1.1e-141 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
AHJIJCLC_01499 | 8.7e-47 | yazA | L | GIY-YIG catalytic domain protein | ||
AHJIJCLC_01500 | 4e-136 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
AHJIJCLC_01501 | 3.3e-115 | plsC | 2.3.1.51 | I | Acyltransferase | |
AHJIJCLC_01502 | 2.7e-27 | yneF | S | Uncharacterised protein family (UPF0154) | ||
AHJIJCLC_01503 | 9.2e-37 | ynzC | S | UPF0291 protein | ||
AHJIJCLC_01504 | 4.2e-115 | 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 | |
AHJIJCLC_01505 | 4.4e-36 | S | VRR_NUC | |||
AHJIJCLC_01506 | 0.0 | S | Virulence-associated protein E | |||
AHJIJCLC_01507 | 1.2e-293 | 2.7.7.7 | L | DNA polymerase A domain | ||
AHJIJCLC_01508 | 5.4e-86 | S | Protein of unknown function (DUF2815) | |||
AHJIJCLC_01509 | 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 | |
AHJIJCLC_01510 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AHJIJCLC_01511 | 8.3e-218 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
AHJIJCLC_01512 | 2.7e-137 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
AHJIJCLC_01513 | 5.1e-153 | 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 | |
AHJIJCLC_01514 | 8.7e-20 | |||||
AHJIJCLC_01515 | 2.1e-59 | |||||
AHJIJCLC_01516 | 3.1e-75 | uspA | T | universal stress protein | ||
AHJIJCLC_01518 | 6.9e-128 | qmcA | O | prohibitin homologues | ||
AHJIJCLC_01519 | 1.6e-219 | glpT | G | Major Facilitator Superfamily | ||
AHJIJCLC_01520 | 5.9e-48 | tkt | 2.2.1.1 | H | 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 | |
AHJIJCLC_01521 | 9.8e-29 | |||||
AHJIJCLC_01522 | 2e-224 | GT2,GT4 | M | Glycosyltransferase, group 2 family protein | ||
AHJIJCLC_01523 | 1.4e-235 | GT2,GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
AHJIJCLC_01524 | 1.2e-45 | 3.4.16.4 | M | Belongs to the peptidase S11 family | ||
AHJIJCLC_01525 | 4e-111 | KT | YcbB domain | |||
AHJIJCLC_01526 | 1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
AHJIJCLC_01527 | 8.2e-171 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
AHJIJCLC_01528 | 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) | |
AHJIJCLC_01529 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AHJIJCLC_01531 | 1.3e-84 | ydcK | S | Belongs to the SprT family | ||
AHJIJCLC_01532 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
AHJIJCLC_01533 | 2.6e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
AHJIJCLC_01534 | 8.5e-284 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
AHJIJCLC_01535 | 1.4e-127 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
AHJIJCLC_01536 | 4.3e-132 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
AHJIJCLC_01537 | 9.6e-115 | |||||
AHJIJCLC_01539 | 1.4e-111 | divIVA | D | DivIVA domain protein | ||
AHJIJCLC_01540 | 1.3e-145 | ylmH | S | S4 domain protein | ||
AHJIJCLC_01541 | 6.8e-41 | yggT | S | YGGT family | ||
AHJIJCLC_01542 | 2.5e-75 | 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 | ||
AHJIJCLC_01543 | 9e-221 | 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 | ||
AHJIJCLC_01544 | 4.2e-224 | 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 | ||
AHJIJCLC_01545 | 8.4e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AHJIJCLC_01546 | 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) |
AHJIJCLC_01547 | 3.4e-146 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AHJIJCLC_01548 | 9.2e-61 | |||||
AHJIJCLC_01549 | 4.7e-208 | lmrP | E | Major Facilitator Superfamily | ||
AHJIJCLC_01550 | 6.3e-244 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
AHJIJCLC_01551 | 1.2e-74 | rplI | J | Binds to the 23S rRNA | ||
AHJIJCLC_01552 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
AHJIJCLC_01553 | 2.1e-35 | 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 | ||
AHJIJCLC_01554 | 6.4e-91 | 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 | ||
AHJIJCLC_01555 | 3.6e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
AHJIJCLC_01556 | 2.8e-70 | K | helix_turn_helix, mercury resistance | |||
AHJIJCLC_01557 | 5.9e-82 | S | Psort location Cytoplasmic, score | |||
AHJIJCLC_01558 | 1.3e-287 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
AHJIJCLC_01559 | 1.1e-95 | wecD | K | Acetyltransferase (GNAT) family | ||
AHJIJCLC_01560 | 6.4e-105 | 3.2.1.17 | NU | mannosyl-glycoprotein | ||
AHJIJCLC_01561 | 5.1e-195 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
AHJIJCLC_01562 | 4.9e-215 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
AHJIJCLC_01563 | 3e-89 | luxS | 4.4.1.21 | H | 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) | |
AHJIJCLC_01564 | 3.5e-38 | S | Cytochrome B5 | |||
AHJIJCLC_01567 | 4.7e-138 | lmrB | EGP | Major facilitator Superfamily | ||
AHJIJCLC_01568 | 1e-22 | XK27_06785 | V | ABC transporter | ||
AHJIJCLC_01569 | 2.3e-99 | K | Transcriptional regulator | |||
AHJIJCLC_01570 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
AHJIJCLC_01571 | 8.2e-173 | L | transposase, IS605 OrfB family | |||
AHJIJCLC_01572 | 2.7e-64 | L | Transposase IS200 like | |||
AHJIJCLC_01573 | 5.4e-242 | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |||
AHJIJCLC_01574 | 2.1e-257 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AHJIJCLC_01575 | 1.6e-88 | ypmB | S | Protein conserved in bacteria | ||
AHJIJCLC_01576 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AHJIJCLC_01577 | 4.9e-168 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
AHJIJCLC_01578 | 1.9e-113 | tnp | L | DDE domain | ||
AHJIJCLC_01579 | 1.2e-68 | |||||
AHJIJCLC_01580 | 5.9e-26 | K | Transcriptional | |||
AHJIJCLC_01581 | 4.2e-256 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
AHJIJCLC_01582 | 1.5e-249 | scrB | 3.2.1.26 | GH32 | G | invertase |
AHJIJCLC_01583 | 1.3e-176 | malR | K | Transcriptional regulator, LacI family | ||
AHJIJCLC_01584 | 5.7e-71 | K | Transcriptional regulator | |||
AHJIJCLC_01585 | 3e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
AHJIJCLC_01586 | 3e-208 | htrA | 3.4.21.107 | O | serine protease | |
AHJIJCLC_01587 | 6e-154 | vicX | 3.1.26.11 | S | domain protein | |
AHJIJCLC_01588 | 9.4e-144 | yycI | S | YycH protein | ||
AHJIJCLC_01589 | 3e-240 | yycH | S | YycH protein | ||
AHJIJCLC_01590 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
AHJIJCLC_01591 | 6.8e-130 | K | response regulator | |||
AHJIJCLC_01592 | 3.5e-202 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
AHJIJCLC_01593 | 1.7e-43 | lacA | S | transferase hexapeptide repeat | ||
AHJIJCLC_01594 | 2.6e-157 | L | Thioesterase-like superfamily | |||
AHJIJCLC_01596 | 3.5e-58 | S | NADPH-dependent FMN reductase | |||
AHJIJCLC_01597 | 6.8e-13 | S | NADPH-dependent FMN reductase | |||
AHJIJCLC_01598 | 2.3e-241 | yfnA | E | amino acid | ||
AHJIJCLC_01599 | 1.6e-233 | V | MatE | |||
AHJIJCLC_01600 | 9e-281 | arlS | 2.7.13.3 | T | Histidine kinase | |
AHJIJCLC_01601 | 5.6e-121 | K | response regulator | |||
AHJIJCLC_01602 | 7.2e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
AHJIJCLC_01603 | 2.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
AHJIJCLC_01604 | 1.7e-215 | ylbM | S | Belongs to the UPF0348 family | ||
AHJIJCLC_01605 | 8.3e-142 | yqeM | Q | Methyltransferase | ||
AHJIJCLC_01606 | 2.1e-58 | 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 | ||
AHJIJCLC_01607 | 7.3e-112 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
AHJIJCLC_01608 | 5.2e-83 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
AHJIJCLC_01609 | 3.3e-86 | uspA | T | Belongs to the universal stress protein A family | ||
AHJIJCLC_01610 | 3.6e-276 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AHJIJCLC_01611 | 2.4e-156 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
AHJIJCLC_01612 | 6.1e-61 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
AHJIJCLC_01613 | 8e-299 | ytgP | S | Polysaccharide biosynthesis protein | ||
AHJIJCLC_01614 | 1.4e-127 | 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 | ||
AHJIJCLC_01615 | 8.3e-176 | 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 | |
AHJIJCLC_01616 | 3.3e-155 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AHJIJCLC_01617 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AHJIJCLC_01618 | 1.4e-290 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
AHJIJCLC_01619 | 4.3e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
AHJIJCLC_01620 | 4.4e-115 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
AHJIJCLC_01621 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
AHJIJCLC_01622 | 5.6e-175 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
AHJIJCLC_01623 | 3.7e-91 | bioY | S | BioY family | ||
AHJIJCLC_01624 | 1.5e-135 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
AHJIJCLC_01625 | 1e-139 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
AHJIJCLC_01626 | 1.8e-33 | 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 | |
AHJIJCLC_01627 | 4.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
AHJIJCLC_01629 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
AHJIJCLC_01630 | 6.4e-128 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
AHJIJCLC_01631 | 9.4e-70 | pncA | Q | Isochorismatase family | ||
AHJIJCLC_01634 | 3.1e-15 | mshQ | U | COG3209 Rhs family protein | ||
AHJIJCLC_01635 | 2.5e-14 | |||||
AHJIJCLC_01637 | 1.9e-54 | |||||
AHJIJCLC_01638 | 3.9e-193 | S | Domain of unknown function DUF87 | |||
AHJIJCLC_01639 | 1.5e-36 | |||||
AHJIJCLC_01640 | 7e-74 | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | |||
AHJIJCLC_01641 | 1.2e-69 | 1.8.4.10, 1.8.4.8 | K | exodeoxyribonuclease I activity | ||
AHJIJCLC_01642 | 1.5e-185 | O | Heat shock 70 kDa protein | |||
AHJIJCLC_01643 | 6.1e-198 | O | Heat shock 70 kDa protein | |||
AHJIJCLC_01644 | 3.6e-29 | 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 | |||
AHJIJCLC_01645 | 2.2e-69 | T | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | |||
AHJIJCLC_01647 | 2.4e-173 | KLT | Protein tyrosine kinase | |||
AHJIJCLC_01648 | 1.3e-156 | KLT | Protein tyrosine kinase | |||
AHJIJCLC_01649 | 7.8e-73 | |||||
AHJIJCLC_01650 | 1.7e-150 | S | Psort location Cytoplasmic, score 8.87 | |||
AHJIJCLC_01651 | 4.2e-74 | spx4 | 1.20.4.1 | P | ArsC family | |
AHJIJCLC_01652 | 9.4e-178 | 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) | |
AHJIJCLC_01653 | 0.0 | recD | 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 | |
AHJIJCLC_01654 | 7.1e-124 | S | Repeat protein | |||
AHJIJCLC_01655 | 4.1e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
AHJIJCLC_01656 | 4e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AHJIJCLC_01657 | 7e-195 | S | amidohydrolase | |||
AHJIJCLC_01658 | 1.5e-92 | S | amidohydrolase | |||
AHJIJCLC_01659 | 1.5e-59 | flgE | N | Flagellar basal body rod FlgEFG protein C-terminal | ||
AHJIJCLC_01660 | 3e-27 | flbD | N | Flagellar protein (FlbD) | ||
AHJIJCLC_01661 | 2.6e-144 | motA | N | MotA/TolQ/ExbB proton channel family | ||
AHJIJCLC_01662 | 1.5e-135 | motB | N | OmpA family | ||
AHJIJCLC_01663 | 1.8e-187 | fliM | N | Flagellar motor switch protein FliM | ||
AHJIJCLC_01664 | 3e-57 | cheY | T | cheY-homologous receiver domain | ||
AHJIJCLC_01665 | 6.7e-75 | flgC | N | Flagellar basal body rod FlgEFG protein C-terminal | ||
AHJIJCLC_01666 | 1.6e-196 | fliN | N | Type III flagellar switch regulator (C-ring) FliN C-term | ||
AHJIJCLC_01667 | 1e-57 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
AHJIJCLC_01668 | 9e-108 | fliP | N | Plays a role in the flagellum-specific transport system | ||
AHJIJCLC_01669 | 2.1e-36 | fliQ | N | Flagellar biosynthetic protein FliQ | ||
AHJIJCLC_01670 | 2.4e-128 | fliR | N | Role in flagellar biosynthesis | ||
AHJIJCLC_01671 | 3.1e-187 | 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 | ||
AHJIJCLC_01672 | 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 | ||
AHJIJCLC_01673 | 3.7e-140 | fliA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
AHJIJCLC_01674 | 1e-131 | flhO | N | Flagellar basal body rod FlgEFG protein C-terminal | ||
AHJIJCLC_01675 | 5.3e-130 | flgG | N | Flagellar basal body rod FlgEFG protein C-terminal | ||
AHJIJCLC_01676 | 1.8e-102 | cheC | NT | CheC-like family | ||
AHJIJCLC_01677 | 6.6e-84 | cheD | 3.5.1.44 | NT | Probably deamidates glutamine residues to glutamate on methyl-accepting chemotaxis receptors (MCPs), playing an important role in chemotaxis | |
AHJIJCLC_01678 | 2e-166 | cheV | T | Two component signalling adaptor domain | ||
AHJIJCLC_01679 | 3.4e-225 | T | HDOD domain | |||
AHJIJCLC_01680 | 2.8e-92 | S | Late competence development protein ComFB | |||
AHJIJCLC_01681 | 5e-137 | D | Cellulose biosynthesis protein BcsQ | |||
AHJIJCLC_01682 | 0.0 | fliD | N | Required for 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 | ||
AHJIJCLC_01683 | 4.3e-59 | fliS | N | Flagellar protein FliS | ||
AHJIJCLC_01684 | 7.8e-62 | |||||
AHJIJCLC_01685 | 3.1e-80 | ftsE | D | ATPases associated with a variety of cellular activities | ||
AHJIJCLC_01686 | 3.1e-217 | S | Uncharacterised nucleotidyltransferase | |||
AHJIJCLC_01687 | 5.1e-190 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |||
AHJIJCLC_01689 | 1.4e-167 | L | ISXO2-like transposase domain | |||
AHJIJCLC_01691 | 2.4e-80 | |||||
AHJIJCLC_01693 | 6.6e-39 | |||||
AHJIJCLC_01696 | 6.2e-123 | S | TIR domain | |||
AHJIJCLC_01697 | 2.9e-32 | |||||
AHJIJCLC_01698 | 1.3e-245 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
AHJIJCLC_01699 | 2.6e-147 | prrC | V | AAA domain | ||
AHJIJCLC_01700 | 6.9e-61 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AHJIJCLC_01701 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
AHJIJCLC_01702 | 2.3e-113 | |||||
AHJIJCLC_01703 | 1.6e-32 | |||||
AHJIJCLC_01704 | 1.6e-15 | |||||
AHJIJCLC_01705 | 9.2e-56 | ampD | 3.5.1.28 | V | Ami_2 | |
AHJIJCLC_01706 | 9e-33 | S | Holin of 3TMs, for gene-transfer release | |||
AHJIJCLC_01708 | 2.1e-45 | |||||
AHJIJCLC_01710 | 5.3e-79 | mleR | K | LysR family | ||
AHJIJCLC_01711 | 1.6e-230 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
AHJIJCLC_01712 | 2.1e-183 | XK27_09615 | S | reductase | ||
AHJIJCLC_01713 | 1.9e-91 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
AHJIJCLC_01714 | 6.1e-223 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
AHJIJCLC_01715 | 3.6e-215 | frdC | 1.3.5.4 | C | FAD binding domain | |
AHJIJCLC_01716 | 1.9e-224 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
AHJIJCLC_01717 | 4.5e-163 | mleR | K | LysR family transcriptional regulator | ||
AHJIJCLC_01718 | 2.7e-252 | yjjP | S | Putative threonine/serine exporter | ||
AHJIJCLC_01719 | 5.5e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
AHJIJCLC_01720 | 2.4e-189 | I | Alpha beta | |||
AHJIJCLC_01721 | 1e-107 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
AHJIJCLC_01722 | 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 | |
AHJIJCLC_01723 | 1.1e-200 | T | COG NOG25714 non supervised orthologous group | |||
AHJIJCLC_01724 | 5.9e-59 | K | Helix-turn-helix domain | |||
AHJIJCLC_01725 | 1.7e-38 | L | Psort location Cytoplasmic, score 8.96 | |||
AHJIJCLC_01726 | 3.9e-270 | L | viral genome integration into host DNA | |||
AHJIJCLC_01727 | 2.3e-53 | S | Mazg nucleotide pyrophosphohydrolase | |||
AHJIJCLC_01728 | 2.3e-136 | E | GDSL-like Lipase/Acylhydrolase family | |||
AHJIJCLC_01729 | 1.1e-123 | C | nitroreductase | |||
AHJIJCLC_01730 | 1.3e-176 | rihA | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
AHJIJCLC_01731 | 2.9e-120 | arcC | 2.7.2.2 | E | Amino acid kinase family | |
AHJIJCLC_01734 | 3.6e-40 | sucD | 6.2.1.5 | C | Protein of unknown function (DUF1116) | |
AHJIJCLC_01735 | 3.4e-69 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Aminotransferase class-V | |
AHJIJCLC_01736 | 9.5e-63 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Aminotransferase class-V | |
AHJIJCLC_01737 | 2.6e-180 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
AHJIJCLC_01738 | 3.2e-256 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
AHJIJCLC_01739 | 1.9e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AHJIJCLC_01740 | 1.4e-130 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
AHJIJCLC_01741 | 1.2e-109 | 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) | |
AHJIJCLC_01742 | 6.9e-47 | |||||
AHJIJCLC_01743 | 3.5e-272 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
AHJIJCLC_01745 | 7.6e-35 | U | EntS YbdA MFS transporter |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)