ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HIDONJMO_00002 | 6.6e-94 | L | Integrase | |||
HIDONJMO_00004 | 2.6e-162 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
HIDONJMO_00005 | 2e-83 | copB | 3.6.3.4 | P | P-type ATPase | |
HIDONJMO_00007 | 8.5e-50 | |||||
HIDONJMO_00012 | 1.8e-175 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
HIDONJMO_00013 | 1e-61 | emrY | EGP | Major facilitator Superfamily | ||
HIDONJMO_00014 | 2.4e-264 | L | PFAM Integrase catalytic region | |||
HIDONJMO_00015 | 1e-86 | L | transposase, IS605 OrfB family | |||
HIDONJMO_00016 | 1e-73 | |||||
HIDONJMO_00017 | 2.7e-24 | |||||
HIDONJMO_00018 | 5.4e-135 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HIDONJMO_00019 | 1.1e-189 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HIDONJMO_00020 | 2.9e-310 | lmrA | V | ABC transporter, ATP-binding protein | ||
HIDONJMO_00021 | 0.0 | yfiC | V | ABC transporter | ||
HIDONJMO_00022 | 1.1e-283 | pipD | E | Dipeptidase | ||
HIDONJMO_00023 | 1.3e-87 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
HIDONJMO_00024 | 1.4e-133 | gntR | K | UbiC transcription regulator-associated domain protein | ||
HIDONJMO_00025 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
HIDONJMO_00026 | 2.7e-244 | yagE | E | amino acid | ||
HIDONJMO_00027 | 4.5e-140 | aroD | S | Serine hydrolase (FSH1) | ||
HIDONJMO_00028 | 9.7e-242 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HIDONJMO_00029 | 5.2e-167 | GK | ROK family | |||
HIDONJMO_00030 | 0.0 | tetP | J | elongation factor G | ||
HIDONJMO_00031 | 5.1e-81 | uspA | T | universal stress protein | ||
HIDONJMO_00032 | 1.1e-194 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
HIDONJMO_00033 | 7.1e-63 | |||||
HIDONJMO_00034 | 5.2e-14 | |||||
HIDONJMO_00035 | 1.4e-212 | EGP | Major facilitator Superfamily | |||
HIDONJMO_00036 | 2.9e-257 | G | PTS system Galactitol-specific IIC component | |||
HIDONJMO_00037 | 2.6e-180 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
HIDONJMO_00038 | 1.1e-161 | |||||
HIDONJMO_00039 | 1e-72 | K | Transcriptional regulator | |||
HIDONJMO_00040 | 3.7e-190 | D | Alpha beta | |||
HIDONJMO_00041 | 2.2e-52 | ypaA | S | Protein of unknown function (DUF1304) | ||
HIDONJMO_00042 | 0.0 | yjcE | P | Sodium proton antiporter | ||
HIDONJMO_00043 | 1.6e-52 | yvlA | ||||
HIDONJMO_00044 | 1.8e-113 | P | Cobalt transport protein | |||
HIDONJMO_00045 | 1e-246 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
HIDONJMO_00046 | 3e-96 | S | ABC-type cobalt transport system, permease component | |||
HIDONJMO_00047 | 3.3e-133 | S | membrane transporter protein | |||
HIDONJMO_00048 | 2.5e-138 | IQ | KR domain | |||
HIDONJMO_00049 | 3.6e-182 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
HIDONJMO_00050 | 1.7e-182 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
HIDONJMO_00051 | 6.7e-150 | L | hmm pf00665 | |||
HIDONJMO_00052 | 9.3e-127 | L | Helix-turn-helix domain | |||
HIDONJMO_00053 | 5.1e-49 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HIDONJMO_00054 | 2.7e-117 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
HIDONJMO_00055 | 3.8e-106 | tra | L | Transposase and inactivated derivatives, IS30 family | ||
HIDONJMO_00056 | 5.3e-204 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
HIDONJMO_00057 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
HIDONJMO_00058 | 2.2e-81 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
HIDONJMO_00059 | 1.7e-187 | hpaIM | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | |
HIDONJMO_00060 | 9.1e-192 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HIDONJMO_00061 | 1.3e-165 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HIDONJMO_00062 | 2.1e-222 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HIDONJMO_00063 | 1.6e-177 | |||||
HIDONJMO_00064 | 3e-130 | cobB | K | SIR2 family | ||
HIDONJMO_00065 | 2.8e-156 | 2.1.1.72 | KL | DNA methylase | ||
HIDONJMO_00066 | 8.1e-238 | L | Transposase | |||
HIDONJMO_00067 | 5e-193 | pipD | E | Dipeptidase | ||
HIDONJMO_00068 | 1.1e-40 | L | Initiator Replication protein | |||
HIDONJMO_00069 | 3.2e-55 | S | Phage head-tail joining protein | |||
HIDONJMO_00070 | 3.6e-70 | S | Bacteriophage holin family | |||
HIDONJMO_00072 | 1.2e-125 | ywfI | S | Chlorite dismutase | ||
HIDONJMO_00074 | 3.8e-26 | S | serine-type endopeptidase activity | |||
HIDONJMO_00075 | 4.3e-43 | S | Phage gp6-like head-tail connector protein | |||
HIDONJMO_00076 | 2.8e-165 | S | Phage capsid family | |||
HIDONJMO_00077 | 2.3e-110 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
HIDONJMO_00078 | 4.7e-114 | 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 | |
HIDONJMO_00079 | 1.3e-35 | ynzC | S | UPF0291 protein | ||
HIDONJMO_00080 | 9.8e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
HIDONJMO_00081 | 4.6e-117 | plsC | 2.3.1.51 | I | Acyltransferase | |
HIDONJMO_00082 | 6.4e-142 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
HIDONJMO_00083 | 5.4e-49 | yazA | L | GIY-YIG catalytic domain protein | ||
HIDONJMO_00084 | 9.8e-183 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HIDONJMO_00085 | 1.2e-143 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HIDONJMO_00086 | 2.4e-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 | ||
HIDONJMO_00087 | 2e-129 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HIDONJMO_00088 | 2.2e-94 | 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 | ||
HIDONJMO_00089 | 9.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HIDONJMO_00090 | 1.3e-137 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
HIDONJMO_00091 | 9.2e-234 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HIDONJMO_00092 | 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 | |
HIDONJMO_00093 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HIDONJMO_00094 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
HIDONJMO_00095 | 1e-215 | nusA | K | Participates in both transcription termination and antitermination | ||
HIDONJMO_00096 | 1e-44 | ylxR | K | Protein of unknown function (DUF448) | ||
HIDONJMO_00097 | 4.5e-49 | ylxQ | J | ribosomal protein | ||
HIDONJMO_00098 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
HIDONJMO_00099 | 2.1e-58 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
HIDONJMO_00100 | 1.8e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HIDONJMO_00101 | 2.9e-176 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
HIDONJMO_00102 | 5.8e-64 | |||||
HIDONJMO_00103 | 4.1e-195 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HIDONJMO_00104 | 2.3e-75 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
HIDONJMO_00105 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
HIDONJMO_00106 | 5.1e-199 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
HIDONJMO_00107 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
HIDONJMO_00108 | 4.1e-275 | pipD | E | Dipeptidase | ||
HIDONJMO_00109 | 4e-198 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
HIDONJMO_00111 | 8e-174 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HIDONJMO_00113 | 2.8e-57 | |||||
HIDONJMO_00114 | 1.1e-178 | prmA | J | Ribosomal protein L11 methyltransferase | ||
HIDONJMO_00115 | 1.2e-129 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
HIDONJMO_00116 | 1.2e-52 | |||||
HIDONJMO_00117 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
HIDONJMO_00118 | 8.4e-78 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
HIDONJMO_00119 | 1e-164 | yniA | G | Phosphotransferase enzyme family | ||
HIDONJMO_00120 | 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) | |
HIDONJMO_00121 | 6.5e-131 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HIDONJMO_00122 | 9.1e-265 | glnPH2 | P | ABC transporter permease | ||
HIDONJMO_00123 | 7.5e-23 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HIDONJMO_00124 | 3.8e-70 | yqeY | S | YqeY-like protein | ||
HIDONJMO_00125 | 1.9e-147 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
HIDONJMO_00126 | 7.2e-192 | L | Transposase | |||
HIDONJMO_00127 | 9.9e-153 | recT | L | RecT family | ||
HIDONJMO_00128 | 4.3e-41 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
HIDONJMO_00129 | 5.5e-45 | yitW | S | Pfam:DUF59 | ||
HIDONJMO_00130 | 4.8e-73 | moaA | 4.1.99.22 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
HIDONJMO_00131 | 6e-21 | arbY | M | family 8 | ||
HIDONJMO_00132 | 4.5e-44 | cbiN | P | Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import | ||
HIDONJMO_00133 | 7.7e-92 | cbiM | P | Part of the energy-coupling factor (ECF) transporter complex CbiMNOQ involved in cobalt import | ||
HIDONJMO_00134 | 6e-22 | L | Helix-turn-helix domain | |||
HIDONJMO_00135 | 1e-38 | arbV | 2.3.1.51 | I | Acyl-transferase | |
HIDONJMO_00136 | 2.8e-17 | |||||
HIDONJMO_00137 | 1.5e-106 | 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) | |
HIDONJMO_00138 | 4.2e-250 | 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 | |
HIDONJMO_00139 | 7.1e-248 | yifK | E | Amino acid permease | ||
HIDONJMO_00140 | 2.6e-291 | clcA | P | chloride | ||
HIDONJMO_00141 | 1.8e-34 | secG | U | Preprotein translocase | ||
HIDONJMO_00142 | 6.8e-147 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
HIDONJMO_00143 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HIDONJMO_00144 | 1.4e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
HIDONJMO_00145 | 6.3e-105 | yxjI | ||||
HIDONJMO_00146 | 6.2e-136 | 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 | |
HIDONJMO_00147 | 3.8e-179 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HIDONJMO_00148 | 2.9e-81 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
HIDONJMO_00149 | 2.6e-86 | K | Acetyltransferase (GNAT) domain | |||
HIDONJMO_00150 | 4.4e-76 | S | PAS domain | |||
HIDONJMO_00151 | 2.7e-102 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HIDONJMO_00152 | 3.6e-168 | murB | 1.3.1.98 | M | Cell wall formation | |
HIDONJMO_00153 | 2.7e-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 | |
HIDONJMO_00154 | 1.7e-66 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
HIDONJMO_00155 | 6.1e-244 | fucP | G | Major Facilitator Superfamily | ||
HIDONJMO_00156 | 5e-151 | 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 | |
HIDONJMO_00157 | 2e-126 | ybbR | S | YbbR-like protein | ||
HIDONJMO_00158 | 9.4e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HIDONJMO_00159 | 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 | |
HIDONJMO_00160 | 8.7e-53 | |||||
HIDONJMO_00161 | 0.0 | oatA | I | Acyltransferase | ||
HIDONJMO_00162 | 2.3e-81 | K | Transcriptional regulator | |||
HIDONJMO_00163 | 5.7e-149 | XK27_02985 | S | Cof-like hydrolase | ||
HIDONJMO_00164 | 2.8e-79 | lytE | M | Lysin motif | ||
HIDONJMO_00166 | 1.5e-132 | K | response regulator | |||
HIDONJMO_00167 | 6.8e-273 | yclK | 2.7.13.3 | T | Histidine kinase | |
HIDONJMO_00168 | 2.6e-155 | glcU | U | sugar transport | ||
HIDONJMO_00169 | 9e-94 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
HIDONJMO_00170 | 1e-262 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HIDONJMO_00171 | 1.3e-28 | |||||
HIDONJMO_00172 | 5.6e-164 | xylR | GK | ROK family | ||
HIDONJMO_00173 | 6.7e-300 | xylB | 2.7.1.17 | G | Belongs to the FGGY kinase family | |
HIDONJMO_00174 | 8.1e-154 | KT | YcbB domain | |||
HIDONJMO_00175 | 3.4e-191 | 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 | |
HIDONJMO_00176 | 4.3e-172 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
HIDONJMO_00177 | 1.1e-240 | E | amino acid | |||
HIDONJMO_00178 | 1.8e-214 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
HIDONJMO_00179 | 4e-226 | yxiO | S | Vacuole effluxer Atg22 like | ||
HIDONJMO_00181 | 9.2e-178 | L | PFAM Integrase catalytic region | |||
HIDONJMO_00182 | 6.4e-09 | ycfA | K | Bacterial regulatory proteins, tetR family | ||
HIDONJMO_00183 | 1.2e-71 | K | Copper transport repressor CopY TcrY | |||
HIDONJMO_00184 | 1.9e-47 | res | 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
HIDONJMO_00185 | 2.1e-126 | |||||
HIDONJMO_00186 | 3.9e-70 | tlpA2 | L | Transposase IS200 like | ||
HIDONJMO_00187 | 9.3e-127 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HIDONJMO_00188 | 7.5e-153 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
HIDONJMO_00189 | 2.7e-26 | K | TRANSCRIPTIONal | |||
HIDONJMO_00190 | 7.9e-61 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
HIDONJMO_00191 | 5.6e-79 | pncA | Q | Isochorismatase family | ||
HIDONJMO_00192 | 4e-230 | 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 | |
HIDONJMO_00193 | 4.2e-111 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
HIDONJMO_00194 | 2.9e-125 | L | PFAM Integrase catalytic region | |||
HIDONJMO_00195 | 3.2e-96 | S | PFAM Archaeal ATPase | |||
HIDONJMO_00196 | 1.3e-46 | |||||
HIDONJMO_00198 | 1.9e-37 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HIDONJMO_00199 | 7.9e-158 | amtB | P | ammonium transporter | ||
HIDONJMO_00200 | 2.1e-249 | gor | 1.8.1.7 | C | pyridine nucleotide-disulfide oxidoreductase | |
HIDONJMO_00201 | 1.8e-90 | S | B3 4 domain | |||
HIDONJMO_00202 | 2.1e-91 | |||||
HIDONJMO_00203 | 4.8e-122 | pnb | C | nitroreductase | ||
HIDONJMO_00204 | 2e-74 | ogt | 2.1.1.63 | L | Methyltransferase | |
HIDONJMO_00205 | 8.5e-172 | XK27_00915 | C | Luciferase-like monooxygenase | ||
HIDONJMO_00206 | 1.5e-153 | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase | |
HIDONJMO_00207 | 7.3e-69 | S | Protein of unknown function (DUF3021) | |||
HIDONJMO_00208 | 6.4e-78 | K | LytTr DNA-binding domain | |||
HIDONJMO_00209 | 2e-91 | K | Acetyltransferase (GNAT) family | |||
HIDONJMO_00210 | 3.1e-21 | |||||
HIDONJMO_00211 | 1.1e-119 | ybhL | S | Belongs to the BI1 family | ||
HIDONJMO_00212 | 6.5e-81 | yjcF | 3.5.4.33, 4.4.1.8 | K | protein acetylation | |
HIDONJMO_00213 | 9.3e-197 | S | Protein of unknown function (DUF3114) | |||
HIDONJMO_00214 | 3.7e-298 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HIDONJMO_00215 | 1.3e-165 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HIDONJMO_00216 | 3.3e-106 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
HIDONJMO_00217 | 9.1e-62 | S | Domain of unknown function (DUF4828) | |||
HIDONJMO_00218 | 4.5e-191 | mocA | S | Oxidoreductase | ||
HIDONJMO_00219 | 8.5e-227 | yfmL | L | DEAD DEAH box helicase | ||
HIDONJMO_00221 | 2.6e-208 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
HIDONJMO_00222 | 9.3e-56 | |||||
HIDONJMO_00223 | 2.3e-67 | gtcA | S | Teichoic acid glycosylation protein | ||
HIDONJMO_00224 | 6.7e-78 | fld | C | Flavodoxin | ||
HIDONJMO_00225 | 1.7e-167 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
HIDONJMO_00226 | 1.7e-220 | arcT | 2.6.1.1 | E | Aminotransferase | |
HIDONJMO_00227 | 3.1e-254 | E | Arginine ornithine antiporter | |||
HIDONJMO_00228 | 1.1e-281 | yjeM | E | Amino Acid | ||
HIDONJMO_00229 | 3.2e-153 | yihY | S | Belongs to the UPF0761 family | ||
HIDONJMO_00230 | 6.6e-34 | S | Protein of unknown function (DUF2922) | |||
HIDONJMO_00231 | 4.9e-31 | |||||
HIDONJMO_00232 | 7.4e-125 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HIDONJMO_00233 | 2.1e-145 | cps1D | M | Domain of unknown function (DUF4422) | ||
HIDONJMO_00234 | 1.1e-175 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
HIDONJMO_00235 | 5e-119 | rfbP | 2.7.8.6 | M | Bacterial sugar transferase | |
HIDONJMO_00236 | 0.0 | 2.7.7.6 | M | Peptidase family M23 | ||
HIDONJMO_00237 | 1.4e-150 | 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 | |
HIDONJMO_00238 | 3.4e-38 | 3.2.1.55 | GH51 | G | Right handed beta helix region | |
HIDONJMO_00239 | 2.2e-83 | S | Protein of unknown function (DUF2815) | |||
HIDONJMO_00240 | 2.3e-120 | GT2,GT4 | LM | gp58-like protein | ||
HIDONJMO_00242 | 3.9e-27 | mleP3 | S | Membrane transport protein | ||
HIDONJMO_00243 | 7.3e-121 | T | Transcriptional regulatory protein, C terminal | |||
HIDONJMO_00244 | 9.9e-239 | T | GHKL domain | |||
HIDONJMO_00245 | 1e-108 | S | Peptidase propeptide and YPEB domain | |||
HIDONJMO_00246 | 1.7e-76 | P | FAD-binding domain | |||
HIDONJMO_00247 | 4.3e-55 | yphJ | 4.1.1.44 | S | decarboxylase | |
HIDONJMO_00248 | 5.3e-83 | K | Bacterial regulatory proteins, tetR family | |||
HIDONJMO_00249 | 2.2e-77 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HIDONJMO_00250 | 8.2e-166 | K | COG COG0846 NAD-dependent protein deacetylases, SIR2 family | |||
HIDONJMO_00251 | 1.6e-165 | S | Oxidoreductase, aldo keto reductase family protein | |||
HIDONJMO_00252 | 2.7e-85 | C | Flavodoxin | |||
HIDONJMO_00253 | 1.4e-156 | K | Transcriptional regulator | |||
HIDONJMO_00254 | 6.3e-88 | lacA | S | transferase hexapeptide repeat | ||
HIDONJMO_00255 | 9.4e-32 | S | thiolester hydrolase activity | |||
HIDONJMO_00256 | 2e-152 | S | Alpha beta hydrolase | |||
HIDONJMO_00257 | 1.5e-92 | padC | Q | Phenolic acid decarboxylase | ||
HIDONJMO_00258 | 3.3e-92 | padR | K | Virulence activator alpha C-term | ||
HIDONJMO_00259 | 4.7e-66 | GM | NAD(P)H-binding | |||
HIDONJMO_00260 | 2.3e-155 | ypuA | S | Protein of unknown function (DUF1002) | ||
HIDONJMO_00261 | 5.2e-184 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
HIDONJMO_00262 | 4.3e-59 | K | Transcriptional regulator | |||
HIDONJMO_00263 | 4.3e-40 | K | Transcriptional regulator | |||
HIDONJMO_00264 | 7.6e-163 | akr5f | 1.1.1.346 | S | reductase | |
HIDONJMO_00265 | 1.8e-104 | K | Transcriptional regulator C-terminal region | |||
HIDONJMO_00266 | 2.1e-74 | S | membrane | |||
HIDONJMO_00267 | 6.1e-88 | S | membrane | |||
HIDONJMO_00268 | 1.2e-112 | GM | NAD(P)H-binding | |||
HIDONJMO_00269 | 1.1e-64 | yneR | ||||
HIDONJMO_00270 | 3.4e-131 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HIDONJMO_00271 | 3.7e-140 | T | EAL domain | |||
HIDONJMO_00272 | 7e-253 | pgaC | GT2 | M | Glycosyl transferase | |
HIDONJMO_00273 | 5.2e-84 | |||||
HIDONJMO_00274 | 1.2e-203 | 2.7.7.65 | T | GGDEF domain | ||
HIDONJMO_00275 | 5e-122 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
HIDONJMO_00276 | 1.3e-256 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
HIDONJMO_00277 | 1.9e-197 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
HIDONJMO_00278 | 2e-92 | folT | S | ECF transporter, substrate-specific component | ||
HIDONJMO_00279 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
HIDONJMO_00280 | 2e-112 | ylbE | GM | NAD dependent epimerase dehydratase family protein | ||
HIDONJMO_00281 | 9.8e-255 | pepC | 3.4.22.40 | E | aminopeptidase | |
HIDONJMO_00282 | 6.5e-210 | EGP | Major facilitator Superfamily | |||
HIDONJMO_00283 | 2.4e-229 | |||||
HIDONJMO_00284 | 7.8e-79 | K | Transcriptional regulator, HxlR family | |||
HIDONJMO_00285 | 3.7e-108 | XK27_02070 | S | Nitroreductase family | ||
HIDONJMO_00286 | 2.5e-52 | hxlR | K | Transcriptional regulator, HxlR family | ||
HIDONJMO_00287 | 3e-119 | GM | NmrA-like family | |||
HIDONJMO_00288 | 1.7e-70 | elaA | S | Gnat family | ||
HIDONJMO_00289 | 1.2e-38 | S | Cytochrome B5 | |||
HIDONJMO_00290 | 8.7e-49 | S | Domain of unknown function (DUF4355) | |||
HIDONJMO_00291 | 1.3e-79 | cobJ | 2.1.1.131, 2.1.1.133, 2.1.1.271, 3.7.1.12, 6.3.5.10 | H | Tetrapyrrole (Corrin/Porphyrin) Methylases | |
HIDONJMO_00293 | 9e-77 | L | Integrase | |||
HIDONJMO_00294 | 1.4e-08 | L | Resolvase, N terminal domain | |||
HIDONJMO_00295 | 5.5e-110 | dedA | S | SNARE-like domain protein | ||
HIDONJMO_00296 | 2.4e-105 | S | Protein of unknown function (DUF1461) | |||
HIDONJMO_00297 | 1.1e-133 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HIDONJMO_00298 | 1.3e-93 | yutD | S | Protein of unknown function (DUF1027) | ||
HIDONJMO_00299 | 2.2e-113 | S | Calcineurin-like phosphoesterase | |||
HIDONJMO_00300 | 2.1e-219 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HIDONJMO_00301 | 1.7e-145 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
HIDONJMO_00303 | 6.3e-70 | |||||
HIDONJMO_00304 | 2.7e-40 | |||||
HIDONJMO_00305 | 8.3e-78 | NU | general secretion pathway protein | |||
HIDONJMO_00306 | 7.1e-47 | comGC | U | competence protein ComGC | ||
HIDONJMO_00307 | 9.5e-181 | comGB | NU | type II secretion system | ||
HIDONJMO_00308 | 2.6e-180 | comGA | NU | Type II IV secretion system protein | ||
HIDONJMO_00309 | 3.5e-132 | yebC | K | Transcriptional regulatory protein | ||
HIDONJMO_00310 | 1.9e-134 | |||||
HIDONJMO_00311 | 1.9e-181 | ccpA | K | catabolite control protein A | ||
HIDONJMO_00312 | 2.7e-210 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HIDONJMO_00313 | 3.5e-26 | |||||
HIDONJMO_00314 | 9.4e-37 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
HIDONJMO_00315 | 3.4e-147 | ykuT | M | mechanosensitive ion channel | ||
HIDONJMO_00316 | 5.2e-153 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | ||
HIDONJMO_00317 | 3.6e-76 | ykuL | S | (CBS) domain | ||
HIDONJMO_00318 | 4.4e-94 | S | Phosphoesterase | |||
HIDONJMO_00319 | 2.7e-103 | 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 | |
HIDONJMO_00320 | 2.1e-143 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HIDONJMO_00321 | 1.3e-96 | yslB | S | Protein of unknown function (DUF2507) | ||
HIDONJMO_00322 | 6.1e-54 | trxA | O | Belongs to the thioredoxin family | ||
HIDONJMO_00323 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
HIDONJMO_00324 | 1e-85 | cvpA | S | Colicin V production protein | ||
HIDONJMO_00325 | 6.1e-48 | yrzB | S | Belongs to the UPF0473 family | ||
HIDONJMO_00326 | 3.6e-76 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HIDONJMO_00327 | 4.1e-43 | yrzL | S | Belongs to the UPF0297 family | ||
HIDONJMO_00328 | 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 | |
HIDONJMO_00329 | 1.4e-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 | |
HIDONJMO_00330 | 4.2e-183 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
HIDONJMO_00331 | 2.8e-31 | yajC | U | Preprotein translocase | ||
HIDONJMO_00332 | 2.6e-189 | tgt_1 | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
HIDONJMO_00333 | 3.4e-191 | 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 | |
HIDONJMO_00334 | 1.9e-101 | 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 | |
HIDONJMO_00335 | 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 | ||
HIDONJMO_00336 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HIDONJMO_00337 | 9.5e-209 | rny | S | Endoribonuclease that initiates mRNA decay | ||
HIDONJMO_00338 | 1.3e-64 | M | Glycosyl transferase, family 2 | |||
HIDONJMO_00340 | 1.5e-134 | S | overlaps another CDS with the same product name | |||
HIDONJMO_00341 | 2.7e-68 | L | Belongs to the 'phage' integrase family | |||
HIDONJMO_00342 | 3.5e-49 | czrA | K | Transcriptional regulator, ArsR family | ||
HIDONJMO_00343 | 7.7e-67 | xtmA | L | Terminase small subunit | ||
HIDONJMO_00344 | 4.8e-09 | S | AI-2E family transporter | |||
HIDONJMO_00346 | 5.5e-07 | |||||
HIDONJMO_00348 | 7.4e-68 | rmaI | K | Transcriptional regulator | ||
HIDONJMO_00349 | 5.4e-235 | EGP | Major facilitator Superfamily | |||
HIDONJMO_00350 | 2.4e-110 | yvyE | 3.4.13.9 | S | YigZ family | |
HIDONJMO_00351 | 1.4e-256 | comFA | L | Helicase C-terminal domain protein | ||
HIDONJMO_00352 | 1.3e-114 | comFC | S | Competence protein | ||
HIDONJMO_00353 | 4.2e-95 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HIDONJMO_00354 | 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 | ||
HIDONJMO_00355 | 1.7e-187 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HIDONJMO_00356 | 3.1e-32 | KT | PspC domain protein | |||
HIDONJMO_00357 | 4.9e-52 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
HIDONJMO_00358 | 3e-176 | 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 | ||
HIDONJMO_00359 | 2.2e-156 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HIDONJMO_00360 | 1.8e-184 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HIDONJMO_00361 | 5.7e-169 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HIDONJMO_00362 | 4.3e-135 | yrjD | S | LUD domain | ||
HIDONJMO_00363 | 7.5e-288 | lutB | C | 4Fe-4S dicluster domain | ||
HIDONJMO_00364 | 3.5e-163 | lutA | C | Cysteine-rich domain | ||
HIDONJMO_00365 | 1.5e-172 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HIDONJMO_00366 | 1.1e-217 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
HIDONJMO_00367 | 1.3e-157 | aatB | ET | PFAM extracellular solute-binding protein, family 3 | ||
HIDONJMO_00368 | 4.6e-88 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
HIDONJMO_00369 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
HIDONJMO_00370 | 2.3e-116 | yfbR | S | HD containing hydrolase-like enzyme | ||
HIDONJMO_00371 | 1.5e-13 | |||||
HIDONJMO_00372 | 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 | ||
HIDONJMO_00373 | 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 | ||
HIDONJMO_00374 | 5.4e-245 | steT | E | amino acid | ||
HIDONJMO_00375 | 1.1e-161 | rapZ | S | Displays ATPase and GTPase activities | ||
HIDONJMO_00376 | 1.4e-186 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HIDONJMO_00377 | 4e-170 | whiA | K | May be required for sporulation | ||
HIDONJMO_00379 | 8.8e-15 | |||||
HIDONJMO_00380 | 2e-239 | glpT | G | Major Facilitator Superfamily | ||
HIDONJMO_00381 | 2.1e-103 | 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 | |
HIDONJMO_00383 | 1.1e-189 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HIDONJMO_00384 | 2.4e-228 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HIDONJMO_00385 | 1.1e-78 | pduO | S | Haem-degrading | ||
HIDONJMO_00387 | 9.2e-75 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
HIDONJMO_00389 | 2.9e-23 | cobU | 2.7.1.156, 2.7.7.62, 6.3.5.10 | H | Cobinamide kinase / cobinamide phosphate guanyltransferase | |
HIDONJMO_00390 | 1.1e-48 | S | Phage antirepressor protein KilAC domain | |||
HIDONJMO_00391 | 1.2e-198 | yagE | E | amino acid | ||
HIDONJMO_00392 | 3.4e-85 | dps | P | Belongs to the Dps family | ||
HIDONJMO_00393 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
HIDONJMO_00394 | 1.1e-177 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
HIDONJMO_00395 | 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 | |
HIDONJMO_00396 | 2e-205 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
HIDONJMO_00397 | 4.5e-146 | potB | P | ABC transporter permease | ||
HIDONJMO_00398 | 1.9e-139 | potC | P | ABC transporter permease | ||
HIDONJMO_00399 | 4.3e-208 | potD | P | ABC transporter | ||
HIDONJMO_00400 | 8.1e-230 | |||||
HIDONJMO_00401 | 7.2e-234 | EGP | Sugar (and other) transporter | |||
HIDONJMO_00402 | 6e-255 | yfnA | E | Amino Acid | ||
HIDONJMO_00403 | 1.2e-73 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
HIDONJMO_00404 | 1.9e-101 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
HIDONJMO_00405 | 1.5e-82 | zur | P | Belongs to the Fur family | ||
HIDONJMO_00406 | 4e-17 | 3.2.1.14 | GH18 | |||
HIDONJMO_00407 | 8.3e-151 | |||||
HIDONJMO_00408 | 5.8e-39 | pspC | KT | PspC domain protein | ||
HIDONJMO_00409 | 1.6e-94 | K | Transcriptional regulator (TetR family) | |||
HIDONJMO_00410 | 1e-216 | V | domain protein | |||
HIDONJMO_00411 | 7.6e-183 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
HIDONJMO_00413 | 6.6e-35 | S | Transglycosylase associated protein | |||
HIDONJMO_00414 | 7.5e-228 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HIDONJMO_00415 | 4.2e-126 | 3.1.3.73 | G | phosphoglycerate mutase | ||
HIDONJMO_00416 | 1.2e-115 | dedA | S | SNARE associated Golgi protein | ||
HIDONJMO_00417 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
HIDONJMO_00418 | 1.1e-35 | Q | pyridine nucleotide-disulphide oxidoreductase | |||
HIDONJMO_00419 | 4.7e-157 | EG | EamA-like transporter family | |||
HIDONJMO_00420 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HIDONJMO_00421 | 4.8e-176 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
HIDONJMO_00422 | 2.1e-224 | S | cog cog1373 | |||
HIDONJMO_00424 | 8.7e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HIDONJMO_00425 | 6.2e-71 | cbiC | 5.4.99.60, 5.4.99.61 | H | Precorrin-8X methylmutase | |
HIDONJMO_00426 | 9e-58 | |||||
HIDONJMO_00427 | 5.4e-43 | |||||
HIDONJMO_00428 | 9.8e-09 | K | DNA-binding helix-turn-helix protein | |||
HIDONJMO_00429 | 2.4e-156 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
HIDONJMO_00430 | 3.7e-54 | |||||
HIDONJMO_00431 | 1.3e-205 | yttB | EGP | Major facilitator Superfamily | ||
HIDONJMO_00432 | 1.5e-234 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HIDONJMO_00433 | 2e-74 | rplI | J | Binds to the 23S rRNA | ||
HIDONJMO_00434 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HIDONJMO_00435 | 1.6e-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 | ||
HIDONJMO_00436 | 3.1e-77 | 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 | ||
HIDONJMO_00437 | 1.2e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HIDONJMO_00438 | 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 | |
HIDONJMO_00439 | 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 | |
HIDONJMO_00440 | 1.2e-205 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
HIDONJMO_00441 | 1.7e-34 | yaaA | S | S4 domain protein YaaA | ||
HIDONJMO_00442 | 6.7e-10 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
HIDONJMO_00443 | 1.6e-81 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
HIDONJMO_00444 | 3.2e-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 | |
HIDONJMO_00445 | 2.2e-251 | 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 | ||
HIDONJMO_00446 | 3.4e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HIDONJMO_00447 | 2e-58 | 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 | |
HIDONJMO_00448 | 4.5e-130 | 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 | ||
HIDONJMO_00449 | 9.7e-130 | jag | S | R3H domain protein | ||
HIDONJMO_00450 | 8.7e-254 | 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 | ||
HIDONJMO_00451 | 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 | ||
HIDONJMO_00452 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
HIDONJMO_00453 | 5.3e-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 | |
HIDONJMO_00454 | 1.9e-247 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
HIDONJMO_00455 | 1.7e-113 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HIDONJMO_00456 | 9.1e-89 | 2.3.1.183 | M | Acetyltransferase GNAT family | ||
HIDONJMO_00457 | 2.7e-160 | S | reductase | |||
HIDONJMO_00459 | 3.6e-288 | S | amidohydrolase | |||
HIDONJMO_00460 | 1e-151 | K | Aminotransferase class I and II | |||
HIDONJMO_00461 | 7.3e-60 | K | Aminotransferase class I and II | |||
HIDONJMO_00462 | 1.9e-13 | azlC | E | azaleucine resistance protein AzlC | ||
HIDONJMO_00464 | 2.8e-28 | M | Glycosyltransferase like family 2 | |||
HIDONJMO_00465 | 8.9e-42 | |||||
HIDONJMO_00466 | 1.8e-68 | L | Integrase core domain | |||
HIDONJMO_00467 | 5.9e-54 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
HIDONJMO_00468 | 1.2e-78 | 2.7.13.3 | T | GHKL domain | ||
HIDONJMO_00470 | 1.3e-260 | S | Putative peptidoglycan binding domain | |||
HIDONJMO_00471 | 3.5e-35 | |||||
HIDONJMO_00472 | 1.9e-69 | bacI | V | MacB-like periplasmic core domain | ||
HIDONJMO_00473 | 2e-169 | L | Transposase and inactivated derivatives IS30 family | |||
HIDONJMO_00474 | 8.2e-233 | cycA | E | Amino acid permease | ||
HIDONJMO_00475 | 4.3e-85 | perR | P | Belongs to the Fur family | ||
HIDONJMO_00476 | 7.6e-253 | EGP | Major facilitator Superfamily | |||
HIDONJMO_00477 | 9.6e-92 | tag | 3.2.2.20 | L | glycosylase | |
HIDONJMO_00478 | 5.6e-217 | 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 | |
HIDONJMO_00479 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HIDONJMO_00480 | 4.9e-41 | |||||
HIDONJMO_00481 | 4.1e-303 | ytgP | S | Polysaccharide biosynthesis protein | ||
HIDONJMO_00482 | 6.5e-151 | 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 | |
HIDONJMO_00483 | 1.6e-276 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
HIDONJMO_00484 | 1.2e-85 | uspA | T | Belongs to the universal stress protein A family | ||
HIDONJMO_00485 | 1.4e-176 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
HIDONJMO_00486 | 5e-116 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
HIDONJMO_00487 | 3.8e-113 | |||||
HIDONJMO_00488 | 1.6e-185 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
HIDONJMO_00489 | 4.4e-161 | 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 | |
HIDONJMO_00490 | 2.1e-32 | |||||
HIDONJMO_00491 | 4.5e-112 | S | CAAX protease self-immunity | |||
HIDONJMO_00492 | 1.6e-42 | |||||
HIDONJMO_00494 | 2.2e-54 | 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 | |
HIDONJMO_00495 | 5.2e-87 | 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) | |
HIDONJMO_00496 | 3.1e-104 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
HIDONJMO_00497 | 4.5e-225 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HIDONJMO_00498 | 2.8e-105 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
HIDONJMO_00499 | 9.3e-217 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
HIDONJMO_00500 | 1.8e-43 | |||||
HIDONJMO_00501 | 3.3e-40 | |||||
HIDONJMO_00503 | 1e-165 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HIDONJMO_00504 | 7.3e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HIDONJMO_00506 | 2.3e-182 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
HIDONJMO_00507 | 3.7e-162 | rrmA | 2.1.1.187 | H | Methyltransferase | |
HIDONJMO_00508 | 3.9e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HIDONJMO_00509 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HIDONJMO_00510 | 1.2e-10 | S | Protein of unknown function (DUF4044) | |||
HIDONJMO_00511 | 7.3e-56 | |||||
HIDONJMO_00512 | 3.1e-77 | mraZ | K | Belongs to the MraZ family | ||
HIDONJMO_00513 | 1.2e-174 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HIDONJMO_00514 | 2.6e-56 | ftsL | D | Cell division protein FtsL | ||
HIDONJMO_00515 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
HIDONJMO_00516 | 3.4e-180 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HIDONJMO_00517 | 2.9e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HIDONJMO_00518 | 3e-204 | 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) |
HIDONJMO_00519 | 8.7e-148 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HIDONJMO_00520 | 6.6e-254 | 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 | ||
HIDONJMO_00521 | 5.3e-226 | 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 | ||
HIDONJMO_00522 | 9.4e-71 | 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 | ||
HIDONJMO_00523 | 3.2e-40 | yggT | S | YGGT family | ||
HIDONJMO_00524 | 1.1e-141 | ylmH | S | S4 domain protein | ||
HIDONJMO_00525 | 1.9e-42 | divIVA | D | DivIVA domain protein | ||
HIDONJMO_00526 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
HIDONJMO_00527 | 4.2e-32 | cspA | K | Cold shock protein | ||
HIDONJMO_00528 | 1.1e-98 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
HIDONJMO_00530 | 1e-125 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
HIDONJMO_00531 | 1.1e-214 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
HIDONJMO_00532 | 1.3e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
HIDONJMO_00533 | 1.8e-225 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
HIDONJMO_00534 | 1.1e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
HIDONJMO_00535 | 9e-119 | S | Repeat protein | |||
HIDONJMO_00536 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
HIDONJMO_00537 | 4e-173 | 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) | |
HIDONJMO_00539 | 4.4e-100 | L | Helix-turn-helix domain | |||
HIDONJMO_00540 | 4.5e-160 | L | hmm pf00665 | |||
HIDONJMO_00541 | 9e-23 | UW | LPXTG-motif cell wall anchor domain protein | |||
HIDONJMO_00542 | 1.9e-170 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
HIDONJMO_00543 | 5.1e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HIDONJMO_00544 | 2.3e-248 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HIDONJMO_00545 | 1.2e-76 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HIDONJMO_00546 | 8.5e-223 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HIDONJMO_00547 | 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) | |
HIDONJMO_00548 | 5.8e-138 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HIDONJMO_00549 | 5.5e-217 | patA | 2.6.1.1 | E | Aminotransferase | |
HIDONJMO_00550 | 3.9e-198 | 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 | |
HIDONJMO_00551 | 8.5e-84 | KT | Putative sugar diacid recognition | |||
HIDONJMO_00552 | 1.7e-219 | EG | GntP family permease | |||
HIDONJMO_00553 | 1e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HIDONJMO_00554 | 7.7e-58 | |||||
HIDONJMO_00556 | 1.2e-133 | mltD | CBM50 | M | NlpC P60 family protein | |
HIDONJMO_00557 | 5.7e-29 | |||||
HIDONJMO_00558 | 5.7e-180 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic | |
HIDONJMO_00559 | 9.8e-32 | ykzG | S | Belongs to the UPF0356 family | ||
HIDONJMO_00560 | 2.4e-78 | |||||
HIDONJMO_00561 | 8.2e-102 | 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 | |
HIDONJMO_00562 | 3e-209 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
HIDONJMO_00563 | 2.4e-181 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
HIDONJMO_00564 | 1.8e-224 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
HIDONJMO_00565 | 4.1e-275 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
HIDONJMO_00566 | 1.4e-47 | yktA | S | Belongs to the UPF0223 family | ||
HIDONJMO_00567 | 2.8e-137 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
HIDONJMO_00568 | 0.0 | typA | T | GTP-binding protein TypA | ||
HIDONJMO_00569 | 2e-222 | ftsW | D | Belongs to the SEDS family | ||
HIDONJMO_00570 | 3e-44 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
HIDONJMO_00571 | 6.5e-99 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
HIDONJMO_00572 | 5.1e-90 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HIDONJMO_00573 | 3.3e-197 | ylbL | T | Belongs to the peptidase S16 family | ||
HIDONJMO_00574 | 2.6e-80 | comEA | L | Competence protein ComEA | ||
HIDONJMO_00575 | 6.9e-89 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HIDONJMO_00576 | 0.0 | comEC | S | Competence protein ComEC | ||
HIDONJMO_00577 | 1.2e-146 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HIDONJMO_00578 | 5.1e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HIDONJMO_00579 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HIDONJMO_00580 | 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 | ||
HIDONJMO_00581 | 3.5e-163 | S | Tetratricopeptide repeat | |||
HIDONJMO_00582 | 3.8e-226 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HIDONJMO_00583 | 2.8e-238 | 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 | ||
HIDONJMO_00584 | 1.4e-234 | 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 | ||
HIDONJMO_00585 | 3.6e-108 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HIDONJMO_00586 | 6.1e-60 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
HIDONJMO_00587 | 1.3e-08 | |||||
HIDONJMO_00588 | 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 | ||
HIDONJMO_00589 | 4e-248 | 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 | ||
HIDONJMO_00590 | 1.3e-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 | |
HIDONJMO_00591 | 6.5e-156 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
HIDONJMO_00592 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
HIDONJMO_00593 | 2.7e-91 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
HIDONJMO_00594 | 2.1e-87 | |||||
HIDONJMO_00596 | 1.8e-124 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HIDONJMO_00597 | 5e-71 | S | Phage tail tube protein, TTP | |||
HIDONJMO_00598 | 2e-32 | bamA | GM | domain, Protein | ||
HIDONJMO_00599 | 1.4e-38 | pstS | P | T5orf172 | ||
HIDONJMO_00600 | 7.4e-134 | K | LysR substrate binding domain | |||
HIDONJMO_00601 | 9.5e-172 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HIDONJMO_00602 | 8.6e-248 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HIDONJMO_00603 | 8.6e-173 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HIDONJMO_00604 | 6e-129 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
HIDONJMO_00605 | 2.5e-115 | 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) | |
HIDONJMO_00606 | 6.2e-114 | thiE | 2.5.1.3, 2.7.6.2, 5.4.2.6 | S | Haloacid dehalogenase-like hydrolase | |
HIDONJMO_00607 | 6.7e-95 | ribA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
HIDONJMO_00608 | 1.1e-236 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
HIDONJMO_00609 | 4.9e-177 | K | AI-2E family transporter | |||
HIDONJMO_00610 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HIDONJMO_00611 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
HIDONJMO_00612 | 1.3e-131 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
HIDONJMO_00613 | 4.3e-83 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HIDONJMO_00614 | 4e-212 | 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) | |
HIDONJMO_00615 | 2e-252 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
HIDONJMO_00616 | 5.7e-132 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HIDONJMO_00617 | 7e-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 | |
HIDONJMO_00618 | 2.3e-127 | 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 | |
HIDONJMO_00619 | 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 | |
HIDONJMO_00620 | 2.2e-276 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HIDONJMO_00621 | 4.4e-194 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HIDONJMO_00622 | 2.8e-105 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
HIDONJMO_00623 | 2.5e-294 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HIDONJMO_00624 | 6.9e-242 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HIDONJMO_00625 | 1e-130 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HIDONJMO_00626 | 1.5e-173 | |||||
HIDONJMO_00627 | 1.3e-240 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
HIDONJMO_00628 | 2e-48 | L | PFAM transposase IS200-family protein | |||
HIDONJMO_00632 | 1.3e-73 | M | PFAM NLP P60 protein | |||
HIDONJMO_00633 | 2.9e-182 | ABC-SBP | S | ABC transporter | ||
HIDONJMO_00634 | 1.1e-153 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
HIDONJMO_00635 | 4.8e-137 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
HIDONJMO_00636 | 2.5e-90 | P | Cadmium resistance transporter | |||
HIDONJMO_00637 | 6.8e-56 | K | Transcriptional regulator, ArsR family | |||
HIDONJMO_00638 | 7.2e-55 | M | Leucine-rich repeat (LRR) protein | |||
HIDONJMO_00639 | 1.6e-236 | mepA | V | MATE efflux family protein | ||
HIDONJMO_00640 | 2.1e-54 | trxA | O | Belongs to the thioredoxin family | ||
HIDONJMO_00641 | 1.5e-130 | terC | P | membrane | ||
HIDONJMO_00642 | 4.5e-166 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HIDONJMO_00643 | 2.2e-168 | corA | P | CorA-like Mg2+ transporter protein | ||
HIDONJMO_00644 | 1.6e-305 | L | Transposase | |||
HIDONJMO_00645 | 1.4e-283 | pipD | E | Dipeptidase | ||
HIDONJMO_00646 | 1.6e-241 | pbuX | F | xanthine permease | ||
HIDONJMO_00647 | 1.8e-251 | nhaC | C | Na H antiporter NhaC | ||
HIDONJMO_00648 | 4e-240 | S | C4-dicarboxylate anaerobic carrier | |||
HIDONJMO_00649 | 1.1e-27 | S | C4-dicarboxylate anaerobic carrier | |||
HIDONJMO_00650 | 8e-125 | pgm3 | 3.1.3.73 | G | phosphoglycerate mutase family | |
HIDONJMO_00651 | 1.3e-41 | |||||
HIDONJMO_00652 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HIDONJMO_00653 | 1.7e-207 | gldA | 1.1.1.6 | C | dehydrogenase | |
HIDONJMO_00654 | 7.5e-123 | S | Alpha beta hydrolase | |||
HIDONJMO_00655 | 3.5e-219 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HIDONJMO_00656 | 2.5e-101 | |||||
HIDONJMO_00658 | 1.4e-124 | yciB | M | ErfK YbiS YcfS YnhG | ||
HIDONJMO_00659 | 1.9e-21 | |||||
HIDONJMO_00662 | 2.8e-73 | |||||
HIDONJMO_00663 | 1.5e-175 | |||||
HIDONJMO_00664 | 7.7e-183 | fecB | P | Periplasmic binding protein | ||
HIDONJMO_00665 | 1.4e-139 | fecE | 3.6.3.34 | HP | AAA domain, putative AbiEii toxin, Type IV TA system | |
HIDONJMO_00666 | 1.8e-128 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
HIDONJMO_00667 | 1.2e-76 | S | Flavodoxin | |||
HIDONJMO_00668 | 3.7e-64 | moaE | 2.8.1.12 | H | MoaE protein | |
HIDONJMO_00669 | 4.9e-35 | moaD | 2.8.1.12 | H | ThiS family | |
HIDONJMO_00670 | 3.9e-218 | narK | P | Transporter, major facilitator family protein | ||
HIDONJMO_00671 | 8.4e-165 | hepT | 2.5.1.30, 2.5.1.90 | H | geranyltranstransferase activity | |
HIDONJMO_00672 | 3.6e-182 | |||||
HIDONJMO_00673 | 1.6e-18 | |||||
HIDONJMO_00674 | 2.3e-116 | nreC | K | PFAM regulatory protein LuxR | ||
HIDONJMO_00675 | 1e-190 | comP | 2.7.13.3 | F | Sensor histidine kinase | |
HIDONJMO_00676 | 3e-44 | |||||
HIDONJMO_00677 | 4.7e-105 | 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 | |
HIDONJMO_00678 | 5.1e-84 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
HIDONJMO_00679 | 8.5e-229 | moeA | 2.10.1.1 | H | MoeA N-terminal region (domain I and II) | |
HIDONJMO_00680 | 3.1e-84 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
HIDONJMO_00681 | 8.8e-187 | moeB | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
HIDONJMO_00682 | 0.0 | narG | 1.7.5.1 | C | Belongs to the prokaryotic molybdopterin-containing oxidoreductase family | |
HIDONJMO_00683 | 0.0 | narH | 1.7.5.1 | C | 4Fe-4S dicluster domain | |
HIDONJMO_00684 | 2.7e-100 | narJ | C | nitrate reductase molybdenum cofactor assembly chaperone | ||
HIDONJMO_00685 | 7.4e-129 | narI | 1.7.5.1 | C | Nitrate reductase | |
HIDONJMO_00686 | 1.1e-195 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HIDONJMO_00687 | 1.2e-152 | EG | EamA-like transporter family | |||
HIDONJMO_00688 | 2.5e-118 | L | Integrase | |||
HIDONJMO_00689 | 1.4e-158 | rssA | S | Phospholipase, patatin family | ||
HIDONJMO_00690 | 3.2e-22 | L | Psort location Cytoplasmic, score | |||
HIDONJMO_00691 | 2.4e-53 | |||||
HIDONJMO_00693 | 3.2e-52 | S | Protein of unknown function (DUF1064) | |||
HIDONJMO_00696 | 9.1e-78 | Q | DNA (cytosine-5-)-methyltransferase activity | |||
HIDONJMO_00697 | 2e-21 | |||||
HIDONJMO_00701 | 4.1e-21 | |||||
HIDONJMO_00702 | 8.2e-62 | rusA | L | Endodeoxyribonuclease RusA | ||
HIDONJMO_00705 | 1.7e-37 | |||||
HIDONJMO_00707 | 1.4e-44 | ps333 | L | Terminase small subunit | ||
HIDONJMO_00708 | 2.7e-140 | S | Pfam:Terminase_3C | |||
HIDONJMO_00709 | 1.7e-133 | S | Phage portal protein, SPP1 Gp6-like | |||
HIDONJMO_00710 | 2.1e-91 | S | Phage minor capsid protein 2 | |||
HIDONJMO_00712 | 1.1e-18 | S | Phage minor structural protein GP20 | |||
HIDONJMO_00713 | 3.2e-97 | |||||
HIDONJMO_00714 | 5.4e-13 | |||||
HIDONJMO_00715 | 1.4e-30 | S | Minor capsid protein | |||
HIDONJMO_00716 | 4.2e-13 | S | Minor capsid protein | |||
HIDONJMO_00717 | 6e-14 | S | Minor capsid protein from bacteriophage | |||
HIDONJMO_00718 | 2.6e-38 | N | domain, Protein | |||
HIDONJMO_00719 | 5.1e-07 | |||||
HIDONJMO_00720 | 1.6e-29 | S | Bacteriophage Gp15 protein | |||
HIDONJMO_00721 | 3e-87 | dnaG | M | NlpC/P60 family | ||
HIDONJMO_00722 | 2.4e-70 | S | Phage tail protein | |||
HIDONJMO_00723 | 4.8e-62 | M | Prophage endopeptidase tail | |||
HIDONJMO_00725 | 2.1e-87 | S | Glycosyltransferase like family | |||
HIDONJMO_00726 | 1.4e-83 | M | Domain of unknown function (DUF4422) | |||
HIDONJMO_00727 | 4.1e-41 | M | biosynthesis protein | |||
HIDONJMO_00728 | 3.3e-97 | cps3F | ||||
HIDONJMO_00729 | 3.1e-98 | M | Glycosyltransferase like family 2 | |||
HIDONJMO_00730 | 2.1e-116 | S | Glycosyltransferase like family 2 | |||
HIDONJMO_00731 | 2.2e-75 | rgpB | GT2 | M | Glycosyl transferase family 2 | |
HIDONJMO_00732 | 4.8e-215 | rfbX | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
HIDONJMO_00733 | 2.8e-218 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
HIDONJMO_00734 | 0.0 | ganB | 3.2.1.89 | G | arabinogalactan | |
HIDONJMO_00735 | 2.1e-25 | |||||
HIDONJMO_00736 | 0.0 | G | Peptidase_C39 like family | |||
HIDONJMO_00737 | 1.6e-157 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
HIDONJMO_00738 | 2.5e-197 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HIDONJMO_00739 | 4.2e-109 | 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 | |
HIDONJMO_00740 | 1.9e-161 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HIDONJMO_00741 | 2.1e-36 | S | Domain of unknown function DUF1829 | |||
HIDONJMO_00742 | 0.0 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
HIDONJMO_00743 | 6e-108 | tdk | 2.7.1.21 | F | thymidine kinase | |
HIDONJMO_00744 | 1.2e-194 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HIDONJMO_00745 | 5.7e-163 | 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 | |
HIDONJMO_00746 | 1e-195 | 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 | |
HIDONJMO_00747 | 9.2e-231 | 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 | |
HIDONJMO_00748 | 6.6e-116 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HIDONJMO_00749 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
HIDONJMO_00750 | 9.9e-192 | yibE | S | overlaps another CDS with the same product name | ||
HIDONJMO_00751 | 6.3e-129 | yibF | S | overlaps another CDS with the same product name | ||
HIDONJMO_00752 | 5e-232 | pyrP | F | Permease | ||
HIDONJMO_00753 | 7.3e-124 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HIDONJMO_00754 | 1.5e-14 | 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 | ||
HIDONJMO_00755 | 1.1e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HIDONJMO_00756 | 5.1e-93 | 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 | ||
HIDONJMO_00757 | 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 | |
HIDONJMO_00758 | 1.9e-164 | 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 | ||
HIDONJMO_00759 | 1.1e-267 | 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 | |
HIDONJMO_00760 | 4.5e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HIDONJMO_00761 | 1.3e-33 | ywzB | S | Protein of unknown function (DUF1146) | ||
HIDONJMO_00762 | 2.1e-241 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HIDONJMO_00763 | 1.9e-178 | mbl | D | Cell shape determining protein MreB Mrl | ||
HIDONJMO_00764 | 1e-31 | S | Protein of unknown function (DUF2969) | |||
HIDONJMO_00765 | 4.1e-220 | rodA | D | Belongs to the SEDS family | ||
HIDONJMO_00766 | 3.3e-46 | gcvH | E | glycine cleavage | ||
HIDONJMO_00767 | 5.3e-217 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HIDONJMO_00768 | 3.8e-251 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
HIDONJMO_00769 | 1.2e-264 | glnP | P | ABC transporter | ||
HIDONJMO_00770 | 1.4e-138 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HIDONJMO_00772 | 3.2e-221 | cycA | E | Amino acid permease | ||
HIDONJMO_00773 | 2.3e-218 | nupG | F | Nucleoside transporter | ||
HIDONJMO_00774 | 5.6e-169 | rihC | 3.2.2.1 | F | Nucleoside | |
HIDONJMO_00775 | 9.4e-161 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
HIDONJMO_00776 | 6.6e-128 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HIDONJMO_00777 | 4.3e-151 | noc | K | Belongs to the ParB family | ||
HIDONJMO_00778 | 3.9e-139 | soj | D | Sporulation initiation inhibitor | ||
HIDONJMO_00779 | 1.7e-154 | spo0J | K | Belongs to the ParB family | ||
HIDONJMO_00780 | 5.4e-32 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
HIDONJMO_00781 | 8.8e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HIDONJMO_00782 | 1.5e-135 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HIDONJMO_00783 | 3.4e-118 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
HIDONJMO_00784 | 2.9e-234 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
HIDONJMO_00785 | 1.1e-234 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
HIDONJMO_00786 | 1.1e-130 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
HIDONJMO_00787 | 9.5e-172 | deoR | K | sugar-binding domain protein | ||
HIDONJMO_00788 | 2.9e-207 | 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 | |
HIDONJMO_00789 | 1.2e-123 | K | response regulator | |||
HIDONJMO_00790 | 4.2e-198 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
HIDONJMO_00791 | 4.1e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HIDONJMO_00793 | 4.3e-13 | K | Transcriptional regulator, TetR family | |||
HIDONJMO_00794 | 6.2e-76 | K | Transcriptional regulator, TetR family | |||
HIDONJMO_00795 | 2.2e-72 | |||||
HIDONJMO_00796 | 4.8e-269 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
HIDONJMO_00797 | 7.9e-261 | tagE2 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase |
HIDONJMO_00798 | 2.4e-277 | M | domain protein | |||
HIDONJMO_00799 | 0.0 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
HIDONJMO_00800 | 9.2e-264 | G | Major Facilitator | |||
HIDONJMO_00801 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HIDONJMO_00802 | 8.1e-207 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HIDONJMO_00803 | 2e-258 | G | Major Facilitator | |||
HIDONJMO_00804 | 1.6e-180 | K | Transcriptional regulator, LacI family | |||
HIDONJMO_00805 | 1.3e-265 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HIDONJMO_00807 | 1.2e-100 | nqr | 1.5.1.36 | S | reductase | |
HIDONJMO_00808 | 8.8e-197 | XK27_09615 | S | reductase | ||
HIDONJMO_00809 | 1.6e-179 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
HIDONJMO_00810 | 7.6e-197 | 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 | ||
HIDONJMO_00811 | 1.9e-228 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
HIDONJMO_00812 | 2.5e-101 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HIDONJMO_00813 | 7.4e-141 | ymfM | S | Helix-turn-helix domain | ||
HIDONJMO_00814 | 3.2e-250 | ymfH | S | Peptidase M16 | ||
HIDONJMO_00815 | 1.6e-230 | ymfF | S | Peptidase M16 inactive domain protein | ||
HIDONJMO_00816 | 2.6e-160 | aatB | ET | ABC transporter substrate-binding protein | ||
HIDONJMO_00817 | 2.1e-117 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HIDONJMO_00818 | 3.2e-102 | glnP | P | ABC transporter permease | ||
HIDONJMO_00819 | 1.2e-91 | mreD | M | rod shape-determining protein MreD | ||
HIDONJMO_00820 | 2.2e-151 | mreC | M | Involved in formation and maintenance of cell shape | ||
HIDONJMO_00821 | 1.7e-179 | mreB | D | cell shape determining protein MreB | ||
HIDONJMO_00822 | 6.8e-121 | radC | L | DNA repair protein | ||
HIDONJMO_00823 | 3.7e-246 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HIDONJMO_00824 | 7.6e-230 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
HIDONJMO_00825 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
HIDONJMO_00826 | 2.8e-310 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
HIDONJMO_00827 | 6.3e-185 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
HIDONJMO_00828 | 1.9e-272 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
HIDONJMO_00829 | 5.6e-261 | S | Uncharacterised protein family (UPF0236) | |||
HIDONJMO_00830 | 1.1e-256 | malT | G | Major Facilitator | ||
HIDONJMO_00831 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
HIDONJMO_00832 | 1.9e-121 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
HIDONJMO_00833 | 5.2e-72 | |||||
HIDONJMO_00834 | 6.3e-87 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
HIDONJMO_00835 | 3.3e-118 | K | response regulator | |||
HIDONJMO_00836 | 5.3e-226 | sptS | 2.7.13.3 | T | Histidine kinase | |
HIDONJMO_00837 | 2.5e-209 | yfeO | P | Voltage gated chloride channel | ||
HIDONJMO_00838 | 1.7e-128 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HIDONJMO_00839 | 6.6e-136 | puuD | S | peptidase C26 | ||
HIDONJMO_00840 | 3.8e-167 | yvgN | C | Aldo keto reductase | ||
HIDONJMO_00841 | 6.1e-48 | 1.14.12.17 | S | Cupin 2, conserved barrel domain protein | ||
HIDONJMO_00842 | 0.0 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
HIDONJMO_00843 | 1.1e-86 | hmpT | S | ECF-type riboflavin transporter, S component | ||
HIDONJMO_00844 | 4.2e-261 | nox | C | NADH oxidase | ||
HIDONJMO_00845 | 2.5e-183 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
HIDONJMO_00846 | 4e-253 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
HIDONJMO_00849 | 0.0 | M | LPXTG-motif cell wall anchor domain protein | |||
HIDONJMO_00850 | 4e-182 | M | LPXTG-motif cell wall anchor domain protein | |||
HIDONJMO_00851 | 0.0 | trxB2 | 1.8.1.9 | C | Thioredoxin domain | |
HIDONJMO_00852 | 2.1e-105 | ahpC | 1.11.1.15 | O | Peroxiredoxin | |
HIDONJMO_00853 | 6.5e-138 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
HIDONJMO_00854 | 1.3e-119 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
HIDONJMO_00857 | 7e-43 | 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 | ||
HIDONJMO_00858 | 3.2e-166 | T | Calcineurin-like phosphoesterase superfamily domain | |||
HIDONJMO_00859 | 2.4e-223 | mdtG | EGP | Major facilitator Superfamily | ||
HIDONJMO_00860 | 3e-130 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
HIDONJMO_00861 | 1.9e-156 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
HIDONJMO_00862 | 1.5e-175 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
HIDONJMO_00863 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
HIDONJMO_00864 | 1.5e-228 | lacS | G | Transporter | ||
HIDONJMO_00865 | 2.1e-107 | lacS | G | Transporter | ||
HIDONJMO_00866 | 1.3e-185 | lacR | K | Transcriptional regulator | ||
HIDONJMO_00867 | 3e-50 | S | CRISPR-associated protein (Cas_Csn2) | |||
HIDONJMO_00868 | 1.7e-37 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HIDONJMO_00869 | 9.8e-113 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HIDONJMO_00870 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
HIDONJMO_00871 | 9.5e-83 | |||||
HIDONJMO_00872 | 2.8e-159 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HIDONJMO_00873 | 1.4e-53 | S | Mazg nucleotide pyrophosphohydrolase | |||
HIDONJMO_00874 | 2.9e-34 | |||||
HIDONJMO_00875 | 3.6e-64 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
HIDONJMO_00876 | 9.9e-261 | yfnA | E | amino acid | ||
HIDONJMO_00877 | 9.9e-143 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HIDONJMO_00878 | 6.9e-92 | 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 | ||
HIDONJMO_00879 | 1.3e-38 | ylqC | S | Belongs to the UPF0109 family | ||
HIDONJMO_00880 | 2.2e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HIDONJMO_00881 | 1.8e-249 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
HIDONJMO_00882 | 1.3e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
HIDONJMO_00883 | 4.1e-180 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
HIDONJMO_00884 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
HIDONJMO_00885 | 4.2e-132 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
HIDONJMO_00886 | 2.9e-38 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HIDONJMO_00887 | 6.1e-188 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
HIDONJMO_00888 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
HIDONJMO_00889 | 7.1e-311 | yloV | S | DAK2 domain fusion protein YloV | ||
HIDONJMO_00890 | 4.7e-58 | asp | S | Asp23 family, cell envelope-related function | ||
HIDONJMO_00891 | 7e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
HIDONJMO_00892 | 1.8e-121 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HIDONJMO_00893 | 1.5e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
HIDONJMO_00894 | 7.5e-166 | 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 | |
HIDONJMO_00895 | 0.0 | KLT | serine threonine protein kinase | |||
HIDONJMO_00896 | 1.1e-130 | stp | 3.1.3.16 | T | phosphatase | |
HIDONJMO_00897 | 9.6e-250 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HIDONJMO_00898 | 4e-173 | 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 | |
HIDONJMO_00899 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
HIDONJMO_00900 | 6.9e-215 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
HIDONJMO_00901 | 7.7e-32 | 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 | |
HIDONJMO_00902 | 4.2e-115 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
HIDONJMO_00903 | 1.7e-54 | |||||
HIDONJMO_00904 | 1.9e-263 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HIDONJMO_00905 | 3.3e-77 | argR | K | Regulates arginine biosynthesis genes | ||
HIDONJMO_00906 | 1.1e-150 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HIDONJMO_00907 | 1.7e-159 | 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 | |
HIDONJMO_00908 | 4.3e-43 | 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 | |
HIDONJMO_00909 | 5.3e-224 | 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 | |
HIDONJMO_00910 | 7.2e-150 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
HIDONJMO_00911 | 1.2e-70 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
HIDONJMO_00912 | 2.2e-70 | yqhY | S | Asp23 family, cell envelope-related function | ||
HIDONJMO_00913 | 1.7e-114 | J | 2'-5' RNA ligase superfamily | |||
HIDONJMO_00914 | 5.1e-201 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HIDONJMO_00915 | 2.1e-131 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
HIDONJMO_00916 | 2.1e-45 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HIDONJMO_00917 | 1.6e-54 | ysxB | J | Cysteine protease Prp | ||
HIDONJMO_00918 | 5.2e-50 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HIDONJMO_00919 | 8.3e-111 | K | Transcriptional regulator | |||
HIDONJMO_00923 | 2.5e-89 | dut | S | Protein conserved in bacteria | ||
HIDONJMO_00924 | 3.9e-174 | |||||
HIDONJMO_00925 | 1e-151 | |||||
HIDONJMO_00926 | 3.7e-51 | S | Iron-sulfur cluster assembly protein | |||
HIDONJMO_00927 | 1.4e-100 | msrA | 1.8.4.11, 1.8.4.12 | C | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
HIDONJMO_00928 | 3.1e-153 | P | Belongs to the nlpA lipoprotein family | |||
HIDONJMO_00929 | 3.9e-12 | |||||
HIDONJMO_00930 | 5.9e-124 | bacI | V | MacB-like periplasmic core domain | ||
HIDONJMO_00931 | 4.4e-129 | V | ABC transporter | |||
HIDONJMO_00932 | 5.7e-144 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
HIDONJMO_00933 | 2.3e-259 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
HIDONJMO_00934 | 8.6e-145 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HIDONJMO_00935 | 3e-147 | E | Glyoxalase-like domain | |||
HIDONJMO_00936 | 1.9e-225 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
HIDONJMO_00937 | 2.9e-96 | S | reductase | |||
HIDONJMO_00939 | 5.2e-87 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HIDONJMO_00940 | 1.1e-175 | ABC-SBP | S | ABC transporter | ||
HIDONJMO_00941 | 1.6e-88 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
HIDONJMO_00942 | 2.5e-215 | htrA | 3.4.21.107 | O | serine protease | |
HIDONJMO_00943 | 4.5e-154 | vicX | 3.1.26.11 | S | domain protein | |
HIDONJMO_00944 | 4.6e-149 | yycI | S | YycH protein | ||
HIDONJMO_00945 | 2.1e-246 | yycH | S | YycH protein | ||
HIDONJMO_00946 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
HIDONJMO_00947 | 6.8e-130 | K | response regulator | |||
HIDONJMO_00949 | 6.2e-310 | lmrA | 3.6.3.44 | V | ABC transporter | |
HIDONJMO_00950 | 3.3e-74 | K | helix_turn_helix multiple antibiotic resistance protein | |||
HIDONJMO_00952 | 4e-264 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
HIDONJMO_00953 | 3.2e-135 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
HIDONJMO_00954 | 2.7e-223 | arcD | U | Amino acid permease | ||
HIDONJMO_00955 | 2e-261 | E | Arginine ornithine antiporter | |||
HIDONJMO_00956 | 4.7e-79 | argR | K | Regulates arginine biosynthesis genes | ||
HIDONJMO_00957 | 4.1e-239 | arcA | 3.5.3.6 | E | Arginine | |
HIDONJMO_00958 | 1.5e-186 | ampC | V | Beta-lactamase | ||
HIDONJMO_00959 | 1.9e-32 | |||||
HIDONJMO_00960 | 0.0 | M | domain protein | |||
HIDONJMO_00961 | 4.5e-91 | |||||
HIDONJMO_00963 | 9.2e-159 | yjcE | P | Sodium proton antiporter | ||
HIDONJMO_00964 | 7.9e-69 | yjcE | P | Sodium proton antiporter | ||
HIDONJMO_00966 | 5.2e-56 | |||||
HIDONJMO_00968 | 4.5e-85 | |||||
HIDONJMO_00969 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
HIDONJMO_00970 | 6.3e-50 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HIDONJMO_00971 | 1.3e-55 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HIDONJMO_00972 | 4.5e-103 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
HIDONJMO_00973 | 9.6e-161 | EG | EamA-like transporter family | |||
HIDONJMO_00974 | 3.9e-133 | K | Transcriptional regulatory protein, C-terminal domain protein | |||
HIDONJMO_00975 | 1.9e-158 | pstS | P | Phosphate | ||
HIDONJMO_00976 | 1.2e-152 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HIDONJMO_00977 | 7.9e-152 | pstA | P | Phosphate transport system permease protein PstA | ||
HIDONJMO_00978 | 2e-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 | |
HIDONJMO_00979 | 5.6e-124 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HIDONJMO_00980 | 2.3e-140 | |||||
HIDONJMO_00981 | 6.5e-243 | ydaM | M | Glycosyl transferase | ||
HIDONJMO_00982 | 7.4e-219 | G | Glycosyl hydrolases family 8 | |||
HIDONJMO_00983 | 3.9e-139 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HIDONJMO_00984 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
HIDONJMO_00985 | 1.7e-238 | ktrB | P | Potassium uptake protein | ||
HIDONJMO_00986 | 1.4e-116 | ktrA | P | domain protein | ||
HIDONJMO_00987 | 1.2e-81 | Q | Methyltransferase | |||
HIDONJMO_00988 | 6.3e-230 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HIDONJMO_00989 | 8.9e-65 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
HIDONJMO_00990 | 1.3e-15 | G | Belongs to the glycosyl hydrolase family 6 | |||
HIDONJMO_00991 | 6.1e-180 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
HIDONJMO_00992 | 7.2e-135 | I | alpha/beta hydrolase fold | |||
HIDONJMO_00993 | 2.8e-170 | lsa | S | ABC transporter | ||
HIDONJMO_01001 | 3.5e-97 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
HIDONJMO_01002 | 4.4e-237 | lmrB | EGP | Major facilitator Superfamily | ||
HIDONJMO_01003 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HIDONJMO_01004 | 2e-111 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
HIDONJMO_01005 | 7.5e-150 | sufD | O | Uncharacterized protein family (UPF0051) | ||
HIDONJMO_01006 | 2.6e-80 | lytE | M | LysM domain protein | ||
HIDONJMO_01007 | 0.0 | oppD | EP | Psort location Cytoplasmic, score | ||
HIDONJMO_01008 | 2.3e-93 | lytE | M | LysM domain protein | ||
HIDONJMO_01009 | 6e-148 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HIDONJMO_01010 | 6.9e-167 | preT | 1.3.1.1 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
HIDONJMO_01011 | 4.5e-236 | preA | 1.3.1.1 | C | 4Fe-4S dicluster domain | |
HIDONJMO_01012 | 8.1e-154 | yeaE | S | Aldo keto | ||
HIDONJMO_01013 | 2.4e-77 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
HIDONJMO_01014 | 2.8e-282 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
HIDONJMO_01015 | 2.9e-78 | S | Psort location Cytoplasmic, score | |||
HIDONJMO_01016 | 7.7e-86 | S | Short repeat of unknown function (DUF308) | |||
HIDONJMO_01017 | 1e-23 | |||||
HIDONJMO_01018 | 2.8e-102 | V | VanZ like family | |||
HIDONJMO_01021 | 6e-42 | O | Bacterial dnaA protein | |||
HIDONJMO_01022 | 8.4e-78 | O | Bacterial dnaA protein | |||
HIDONJMO_01023 | 3.2e-236 | L | Integrase core domain | |||
HIDONJMO_01024 | 1.8e-240 | yhjE | EGP | MFS transporter, metabolite H symporter (MHS) family protein | ||
HIDONJMO_01025 | 9.3e-130 | IQ | Dehydrogenase reductase | |||
HIDONJMO_01026 | 2.9e-37 | |||||
HIDONJMO_01027 | 4.8e-114 | ywnB | S | NAD(P)H-binding | ||
HIDONJMO_01028 | 1.2e-38 | S | Cytochrome b5-like Heme/Steroid binding domain | |||
HIDONJMO_01029 | 8e-255 | nhaC | C | Na H antiporter NhaC | ||
HIDONJMO_01030 | 7.7e-183 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
HIDONJMO_01032 | 5e-44 | ydeN | S | Serine hydrolase | ||
HIDONJMO_01033 | 1.3e-61 | psiE | S | Phosphate-starvation-inducible E | ||
HIDONJMO_01034 | 2.5e-141 | 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) | |
HIDONJMO_01036 | 5.9e-177 | S | Aldo keto reductase | |||
HIDONJMO_01037 | 7.6e-75 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | PAP2 superfamily | ||
HIDONJMO_01038 | 0.0 | L | Helicase C-terminal domain protein | |||
HIDONJMO_01040 | 3.2e-253 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
HIDONJMO_01041 | 3.3e-55 | S | Sugar efflux transporter for intercellular exchange | |||
HIDONJMO_01042 | 1.4e-20 | |||||
HIDONJMO_01043 | 0.0 | L | Helicase C-terminal domain protein | |||
HIDONJMO_01044 | 3.3e-47 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
HIDONJMO_01045 | 2.5e-261 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HIDONJMO_01046 | 5.6e-186 | yegS | 2.7.1.107 | G | Lipid kinase | |
HIDONJMO_01047 | 1.8e-275 | 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) | |
HIDONJMO_01048 | 2.7e-277 | 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) | |
HIDONJMO_01049 | 2.4e-50 | 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) | |
HIDONJMO_01050 | 3.3e-203 | camS | S | sex pheromone | ||
HIDONJMO_01051 | 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 | |
HIDONJMO_01052 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HIDONJMO_01053 | 1.1e-211 | 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 | |
HIDONJMO_01054 | 3e-99 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
HIDONJMO_01055 | 3.6e-114 | acmC | 3.2.1.96 | NU | mannosyl-glycoprotein | |
HIDONJMO_01056 | 3.6e-140 | IQ | reductase | |||
HIDONJMO_01057 | 6.9e-178 | rihA | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HIDONJMO_01058 | 8.5e-193 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
HIDONJMO_01059 | 1.2e-95 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
HIDONJMO_01060 | 2.5e-225 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
HIDONJMO_01061 | 2e-77 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
HIDONJMO_01062 | 6.2e-102 | T | Ion transport 2 domain protein | |||
HIDONJMO_01063 | 0.0 | S | Bacterial membrane protein YfhO | |||
HIDONJMO_01064 | 5e-202 | G | Transporter, major facilitator family protein | |||
HIDONJMO_01065 | 2.1e-108 | yvrI | K | sigma factor activity | ||
HIDONJMO_01066 | 3.5e-64 | ydiI | Q | Thioesterase superfamily | ||
HIDONJMO_01067 | 5.8e-157 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
HIDONJMO_01068 | 2.9e-273 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
HIDONJMO_01069 | 5.5e-19 | |||||
HIDONJMO_01070 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HIDONJMO_01071 | 4.2e-32 | feoA | P | FeoA domain | ||
HIDONJMO_01072 | 6.5e-145 | sufC | O | FeS assembly ATPase SufC | ||
HIDONJMO_01073 | 7.3e-239 | sufD | O | FeS assembly protein SufD | ||
HIDONJMO_01074 | 3.3e-60 | 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 | |
HIDONJMO_01075 | 7e-130 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
HIDONJMO_01076 | 7.3e-103 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
HIDONJMO_01077 | 8.6e-198 | 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 | |
HIDONJMO_01078 | 4.7e-132 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HIDONJMO_01079 | 1.9e-228 | 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 | |
HIDONJMO_01080 | 1.4e-136 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HIDONJMO_01081 | 6.6e-142 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
HIDONJMO_01082 | 2.5e-225 | mtnE | 2.6.1.83 | E | Aminotransferase | |
HIDONJMO_01083 | 4e-181 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HIDONJMO_01084 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
HIDONJMO_01085 | 1.4e-113 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HIDONJMO_01087 | 1.1e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HIDONJMO_01088 | 1.9e-292 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HIDONJMO_01089 | 8.2e-82 | S | YbaK proline--tRNA ligase associated domain protein | |||
HIDONJMO_01090 | 4.3e-305 | ybeC | E | amino acid | ||
HIDONJMO_01091 | 0.0 | ydaO | E | amino acid | ||
HIDONJMO_01092 | 9.2e-40 | |||||
HIDONJMO_01093 | 6.8e-202 | pbuG | S | permease | ||
HIDONJMO_01094 | 4.1e-261 | frc | 2.8.3.16 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HIDONJMO_01095 | 0.0 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
HIDONJMO_01096 | 2.5e-135 | S | Belongs to the UPF0246 family | |||
HIDONJMO_01097 | 2.5e-138 | S | Membrane | |||
HIDONJMO_01098 | 8.1e-75 | 4.4.1.5 | E | Glyoxalase | ||
HIDONJMO_01099 | 1.5e-21 | |||||
HIDONJMO_01100 | 7.1e-86 | yueI | S | Protein of unknown function (DUF1694) | ||
HIDONJMO_01101 | 1.7e-235 | rarA | L | recombination factor protein RarA | ||
HIDONJMO_01102 | 4.4e-46 | |||||
HIDONJMO_01103 | 4.3e-83 | usp6 | T | universal stress protein | ||
HIDONJMO_01104 | 2.8e-207 | araR | K | Transcriptional regulator | ||
HIDONJMO_01105 | 3.5e-157 | ytbE | 1.1.1.346 | S | Aldo keto reductase | |
HIDONJMO_01106 | 1.1e-93 | maa | 2.3.1.79 | S | Maltose O-acetyltransferase | |
HIDONJMO_01107 | 1.3e-284 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
HIDONJMO_01108 | 1.8e-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 | |
HIDONJMO_01109 | 0.0 | araB | 2.7.1.12, 2.7.1.16 | G | carbohydrate kinase FGGY | |
HIDONJMO_01110 | 2.6e-261 | araP | U | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
HIDONJMO_01111 | 1.8e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HIDONJMO_01112 | 2.8e-154 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
HIDONJMO_01113 | 4.7e-191 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HIDONJMO_01114 | 3.1e-103 | metI | P | ABC transporter permease | ||
HIDONJMO_01115 | 7e-217 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
HIDONJMO_01116 | 1.2e-252 | clcA | P | chloride | ||
HIDONJMO_01117 | 6.9e-77 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
HIDONJMO_01118 | 4.5e-104 | proW | P | ABC transporter, permease protein | ||
HIDONJMO_01119 | 1e-139 | proV | E | ABC transporter, ATP-binding protein | ||
HIDONJMO_01120 | 6.3e-109 | proWZ | P | ABC transporter permease | ||
HIDONJMO_01121 | 2.3e-162 | proX | M | ABC transporter, substrate-binding protein, QAT family | ||
HIDONJMO_01122 | 9e-75 | K | Transcriptional regulator | |||
HIDONJMO_01123 | 4.8e-154 | 1.6.5.2 | GM | NAD(P)H-binding | ||
HIDONJMO_01125 | 3.3e-217 | 5.4.2.7 | G | Metalloenzyme superfamily | ||
HIDONJMO_01126 | 0.0 | cadA | P | P-type ATPase | ||
HIDONJMO_01127 | 8.2e-110 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
HIDONJMO_01128 | 4.2e-194 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HIDONJMO_01129 | 5.3e-173 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HIDONJMO_01130 | 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) | |
HIDONJMO_01131 | 3.2e-278 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
HIDONJMO_01132 | 1.5e-135 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
HIDONJMO_01133 | 2e-155 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HIDONJMO_01134 | 5.9e-58 | yabA | L | Involved in initiation control of chromosome replication | ||
HIDONJMO_01135 | 8.2e-185 | holB | 2.7.7.7 | L | DNA polymerase III | |
HIDONJMO_01136 | 7.6e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
HIDONJMO_01137 | 4.8e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HIDONJMO_01138 | 9.7e-39 | S | Protein of unknown function (DUF2508) | |||
HIDONJMO_01139 | 3.3e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
HIDONJMO_01140 | 7e-47 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
HIDONJMO_01141 | 6.2e-292 | 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 | |
HIDONJMO_01142 | 3.5e-91 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HIDONJMO_01143 | 3.4e-35 | nrdH | O | Glutaredoxin | ||
HIDONJMO_01144 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HIDONJMO_01145 | 3.4e-199 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HIDONJMO_01146 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HIDONJMO_01147 | 6.4e-126 | S | Putative adhesin | |||
HIDONJMO_01148 | 1.6e-82 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
HIDONJMO_01149 | 4e-56 | K | transcriptional regulator PadR family | |||
HIDONJMO_01150 | 2e-40 | 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 | ||
HIDONJMO_01152 | 7.6e-230 | L | Integrase core domain | |||
HIDONJMO_01153 | 5.1e-139 | L | Bacterial dnaA protein | |||
HIDONJMO_01154 | 5.7e-38 | |||||
HIDONJMO_01155 | 3.2e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HIDONJMO_01156 | 1.7e-82 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HIDONJMO_01157 | 9e-209 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
HIDONJMO_01158 | 8.1e-241 | M | Glycosyl transferase family group 2 | |||
HIDONJMO_01160 | 1.3e-226 | aadAT | EK | Aminotransferase, class I | ||
HIDONJMO_01161 | 3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HIDONJMO_01162 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HIDONJMO_01163 | 3.4e-97 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HIDONJMO_01164 | 2.2e-16 | 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 | ||
HIDONJMO_01165 | 1.4e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HIDONJMO_01166 | 2.3e-136 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HIDONJMO_01167 | 2.1e-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) | ||
HIDONJMO_01168 | 1.7e-273 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HIDONJMO_01169 | 1.7e-207 | yacL | S | domain protein | ||
HIDONJMO_01170 | 2.3e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
HIDONJMO_01171 | 2e-97 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
HIDONJMO_01172 | 1.5e-49 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
HIDONJMO_01173 | 2.6e-126 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HIDONJMO_01174 | 5.1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HIDONJMO_01175 | 7.4e-141 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HIDONJMO_01176 | 1.4e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HIDONJMO_01177 | 2.4e-119 | tcyB | E | ABC transporter | ||
HIDONJMO_01178 | 9.4e-214 | metC | 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
HIDONJMO_01179 | 3.1e-169 | I | alpha/beta hydrolase fold | |||
HIDONJMO_01180 | 1.2e-134 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HIDONJMO_01181 | 0.0 | S | Bacterial membrane protein, YfhO | |||
HIDONJMO_01182 | 3.8e-184 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
HIDONJMO_01183 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
HIDONJMO_01185 | 5.6e-85 | ydcK | S | Belongs to the SprT family | ||
HIDONJMO_01186 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
HIDONJMO_01187 | 5.1e-153 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
HIDONJMO_01188 | 1.7e-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 | |
HIDONJMO_01189 | 1.8e-127 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
HIDONJMO_01190 | 1.4e-133 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
HIDONJMO_01191 | 9.5e-300 | aspT | P | Predicted Permease Membrane Region | ||
HIDONJMO_01192 | 2.8e-252 | EGP | Major facilitator Superfamily | |||
HIDONJMO_01193 | 5.5e-110 | |||||
HIDONJMO_01196 | 1.4e-158 | yjjH | S | Calcineurin-like phosphoesterase | ||
HIDONJMO_01197 | 5e-263 | dtpT | U | amino acid peptide transporter | ||
HIDONJMO_01198 | 3.7e-19 | |||||
HIDONJMO_01200 | 3.7e-91 | yqiG | C | Oxidoreductase | ||
HIDONJMO_01201 | 7.8e-20 | yqiG | C | Oxidoreductase | ||
HIDONJMO_01202 | 1.1e-50 | yqiG | C | Oxidoreductase | ||
HIDONJMO_01203 | 8.5e-54 | S | macrophage migration inhibitory factor | |||
HIDONJMO_01204 | 2.4e-65 | K | HxlR-like helix-turn-helix | |||
HIDONJMO_01205 | 2.1e-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 | |
HIDONJMO_01207 | 9.4e-225 | L | Transposase IS66 family | |||
HIDONJMO_01208 | 1.6e-126 | O | Bacterial dnaA protein | |||
HIDONJMO_01209 | 1.1e-07 | UW | Hep Hag repeat protein | |||
HIDONJMO_01210 | 3.6e-17 | sraP | UW | this gene contains a nucleotide ambiguity which may be the result of a sequencing error | ||
HIDONJMO_01212 | 7.9e-196 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
HIDONJMO_01213 | 1.1e-225 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
HIDONJMO_01214 | 0.0 | secA2 | 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 | ||
HIDONJMO_01215 | 1.3e-154 | asp3 | S | Accessory Sec secretory system ASP3 | ||
HIDONJMO_01216 | 2.4e-217 | asp2 | 3.4.11.5 | S | Accessory Sec system GspB-transporter | |
HIDONJMO_01217 | 2.6e-195 | M | transferase activity, transferring glycosyl groups | |||
HIDONJMO_01218 | 2.8e-144 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
HIDONJMO_01219 | 2.6e-191 | nss | M | transferase activity, transferring glycosyl groups | ||
HIDONJMO_01222 | 3.1e-104 | wecD3 | K | PFAM GCN5-related N-acetyltransferase | ||
HIDONJMO_01223 | 7.2e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HIDONJMO_01224 | 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 | |
HIDONJMO_01225 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HIDONJMO_01226 | 1.5e-172 | malR | K | Transcriptional regulator, LacI family | ||
HIDONJMO_01227 | 2.4e-212 | phbA | 2.3.1.9 | I | Belongs to the thiolase family | |
HIDONJMO_01228 | 1.5e-143 | L | PFAM Integrase catalytic region | |||
HIDONJMO_01229 | 1.7e-281 | 2.4.1.5 | GH13 | G | Glycosyl hydrolase family 70 | |
HIDONJMO_01230 | 5.9e-164 | tnp2 | L | PFAM Transposase, IS204 IS1001 IS1096 IS1165 | ||
HIDONJMO_01231 | 0.0 | gtfC | 2.4.1.5 | GH13 | G | Glycosyl hydrolase family 70 |
HIDONJMO_01232 | 6.9e-30 | S | Acyltransferase family | |||
HIDONJMO_01234 | 4.8e-221 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
HIDONJMO_01235 | 3.4e-296 | 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) | |
HIDONJMO_01236 | 2.4e-261 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HIDONJMO_01237 | 3.3e-177 | 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) | |
HIDONJMO_01238 | 5.9e-22 | S | Protein of unknown function (DUF3042) | |||
HIDONJMO_01239 | 3.4e-67 | yqhL | P | Rhodanese-like protein | ||
HIDONJMO_01240 | 2.8e-182 | glk | 2.7.1.2 | G | Glucokinase | |
HIDONJMO_01241 | 7.4e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
HIDONJMO_01242 | 3.8e-46 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
HIDONJMO_01243 | 3.4e-12 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
HIDONJMO_01244 | 2.6e-100 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HIDONJMO_01245 | 4.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HIDONJMO_01246 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
HIDONJMO_01247 | 0.0 | S | membrane | |||
HIDONJMO_01248 | 8.8e-71 | yneR | S | Belongs to the HesB IscA family | ||
HIDONJMO_01249 | 3.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HIDONJMO_01250 | 1.5e-118 | 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 | ||
HIDONJMO_01251 | 5.5e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HIDONJMO_01252 | 5.7e-46 | 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 | ||
HIDONJMO_01253 | 4.2e-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 | ||
HIDONJMO_01254 | 1.4e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HIDONJMO_01255 | 4.8e-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 | ||
HIDONJMO_01256 | 6.1e-112 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HIDONJMO_01257 | 3.5e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HIDONJMO_01258 | 8.4e-28 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HIDONJMO_01259 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HIDONJMO_01260 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HIDONJMO_01261 | 2.6e-49 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HIDONJMO_01262 | 1.4e-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 | ||
HIDONJMO_01263 | 4e-29 | 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 | ||
HIDONJMO_01264 | 1.3e-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 | ||
HIDONJMO_01265 | 1.6e-94 | 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 | ||
HIDONJMO_01266 | 6.6e-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 | ||
HIDONJMO_01267 | 2.2e-85 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HIDONJMO_01268 | 2.9e-24 | rpmD | J | Ribosomal protein L30 | ||
HIDONJMO_01269 | 8.9e-64 | rplO | J | Binds to the 23S rRNA | ||
HIDONJMO_01270 | 8.8e-240 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
HIDONJMO_01271 | 8.1e-125 | 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 | |
HIDONJMO_01272 | 5.9e-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 | ||
HIDONJMO_01273 | 1.4e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HIDONJMO_01274 | 4.7e-58 | 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 | ||
HIDONJMO_01275 | 2.3e-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 | ||
HIDONJMO_01276 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HIDONJMO_01277 | 1.1e-62 | rplQ | J | Ribosomal protein L17 | ||
HIDONJMO_01278 | 1.9e-80 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HIDONJMO_01279 | 1.6e-271 | sufB | O | assembly protein SufB | ||
HIDONJMO_01280 | 1.4e-56 | yitW | S | Iron-sulfur cluster assembly protein | ||
HIDONJMO_01281 | 6.1e-160 | hipB | K | Helix-turn-helix | ||
HIDONJMO_01282 | 1.3e-114 | nreC | K | PFAM regulatory protein LuxR | ||
HIDONJMO_01283 | 9.2e-39 | S | Cytochrome B5 | |||
HIDONJMO_01284 | 5.8e-157 | yitU | 3.1.3.104 | S | hydrolase | |
HIDONJMO_01285 | 1e-259 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
HIDONJMO_01286 | 4e-148 | f42a | O | Band 7 protein | ||
HIDONJMO_01287 | 0.0 | lytS | 2.7.13.3 | T | LytS YhcK-type transmembrane receptor domain protein | |
HIDONJMO_01288 | 2.4e-130 | lytT | K | response regulator receiver | ||
HIDONJMO_01289 | 1.9e-66 | lrgA | S | LrgA family | ||
HIDONJMO_01290 | 2.6e-124 | lrgB | M | LrgB-like family | ||
HIDONJMO_01291 | 2.1e-160 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HIDONJMO_01292 | 2.1e-95 | L | Helix-turn-helix domain | |||
HIDONJMO_01293 | 1.6e-67 | yqkB | S | Belongs to the HesB IscA family | ||
HIDONJMO_01294 | 2.7e-49 | |||||
HIDONJMO_01296 | 1.2e-88 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
HIDONJMO_01297 | 1.3e-61 | asp | S | Asp23 family, cell envelope-related function | ||
HIDONJMO_01298 | 2.1e-25 | |||||
HIDONJMO_01299 | 4.2e-95 | |||||
HIDONJMO_01300 | 2.4e-289 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
HIDONJMO_01301 | 9.9e-183 | K | Transcriptional regulator, LacI family | |||
HIDONJMO_01302 | 1.9e-11 | gntT | EG | Gluconate | ||
HIDONJMO_01303 | 1.7e-109 | gntT | EG | Gluconate | ||
HIDONJMO_01304 | 4.9e-66 | gntT | EG | Gluconate | ||
HIDONJMO_01305 | 2.9e-295 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
HIDONJMO_01306 | 2.9e-96 | K | Acetyltransferase (GNAT) domain | |||
HIDONJMO_01307 | 5.4e-47 | |||||
HIDONJMO_01308 | 2.4e-22 | |||||
HIDONJMO_01309 | 2.2e-44 | |||||
HIDONJMO_01310 | 1.1e-57 | yhaI | S | Protein of unknown function (DUF805) | ||
HIDONJMO_01311 | 1.3e-17 | |||||
HIDONJMO_01312 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
HIDONJMO_01313 | 2.2e-207 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
HIDONJMO_01314 | 3.7e-176 | M | Glycosyl hydrolases family 25 | |||
HIDONJMO_01315 | 1.4e-144 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
HIDONJMO_01316 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
HIDONJMO_01317 | 3.3e-06 | D | nuclear chromosome segregation | |||
HIDONJMO_01318 | 5.9e-30 | |||||
HIDONJMO_01319 | 7.1e-08 | T | Toxin-antitoxin system, toxin component, MazF family | |||
HIDONJMO_01321 | 1.5e-39 | ykuJ | S | Protein of unknown function (DUF1797) | ||
HIDONJMO_01322 | 2.5e-178 | mprF | I | 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 | ||
HIDONJMO_01323 | 7.2e-197 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
HIDONJMO_01324 | 3e-226 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
HIDONJMO_01325 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
HIDONJMO_01326 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
HIDONJMO_01327 | 2.9e-27 | |||||
HIDONJMO_01328 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
HIDONJMO_01329 | 2.4e-99 | S | Pfam:DUF3816 | |||
HIDONJMO_01330 | 8e-142 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
HIDONJMO_01331 | 6.7e-114 | |||||
HIDONJMO_01332 | 3.6e-157 | V | ABC transporter, ATP-binding protein | |||
HIDONJMO_01333 | 9.3e-65 | gntR1 | K | Transcriptional regulator, GntR family | ||
HIDONJMO_01334 | 1.4e-96 | epsB | M | biosynthesis protein | ||
HIDONJMO_01335 | 1.7e-107 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
HIDONJMO_01336 | 2.6e-09 | capM | M | Psort location CytoplasmicMembrane, score | ||
HIDONJMO_01337 | 1.9e-33 | pglC | M | Bacterial sugar transferase | ||
HIDONJMO_01338 | 5.9e-86 | GT4 | G | Glycosyl transferase 4-like | ||
HIDONJMO_01339 | 5.2e-67 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
HIDONJMO_01340 | 3.2e-42 | M | cog cog1442 | |||
HIDONJMO_01342 | 5.7e-73 | cps2I | S | Psort location CytoplasmicMembrane, score | ||
HIDONJMO_01343 | 1.2e-28 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
HIDONJMO_01344 | 1.9e-29 | M | PFAM Glycosyl transferase family 2 | |||
HIDONJMO_01345 | 1.8e-27 | M | Glycosyltransferase, group 2 family protein | |||
HIDONJMO_01346 | 1.2e-48 | S | Glycosyltransferase like family 2 | |||
HIDONJMO_01347 | 3.6e-162 | yunF | F | Protein of unknown function DUF72 | ||
HIDONJMO_01348 | 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 | |
HIDONJMO_01349 | 1.9e-155 | tatD | L | hydrolase, TatD family | ||
HIDONJMO_01350 | 3.2e-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 | |
HIDONJMO_01351 | 5.2e-159 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
HIDONJMO_01352 | 6.8e-37 | veg | S | Biofilm formation stimulator VEG | ||
HIDONJMO_01353 | 4.9e-159 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
HIDONJMO_01354 | 8.2e-168 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HIDONJMO_01355 | 1.4e-121 | fhuC | P | ABC transporter | ||
HIDONJMO_01356 | 1.4e-118 | znuB | U | ABC 3 transport family | ||
HIDONJMO_01357 | 2.6e-149 | purR | 2.4.2.7 | F | pur operon repressor | |
HIDONJMO_01358 | 7.5e-242 | 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 | |
HIDONJMO_01359 | 1.1e-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) | |
HIDONJMO_01360 | 2.1e-49 | |||||
HIDONJMO_01361 | 2.5e-147 | yxeH | S | hydrolase | ||
HIDONJMO_01362 | 5e-270 | ywfO | S | HD domain protein | ||
HIDONJMO_01363 | 7.9e-146 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
HIDONJMO_01364 | 3e-66 | ywiB | S | Domain of unknown function (DUF1934) | ||
HIDONJMO_01365 | 8.7e-51 | 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 | ||
HIDONJMO_01366 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
HIDONJMO_01367 | 5.7e-236 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HIDONJMO_01368 | 4.6e-41 | rpmE2 | J | Ribosomal protein L31 | ||
HIDONJMO_01369 | 7.7e-236 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
HIDONJMO_01370 | 1.3e-165 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HIDONJMO_01371 | 5.1e-125 | srtA | 3.4.22.70 | M | sortase family | |
HIDONJMO_01372 | 9.5e-234 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
HIDONJMO_01373 | 2.3e-139 | 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) | |
HIDONJMO_01374 | 1.4e-161 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
HIDONJMO_01375 | 4.6e-120 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
HIDONJMO_01376 | 1.5e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HIDONJMO_01377 | 7e-93 | lemA | S | LemA family | ||
HIDONJMO_01378 | 2.6e-158 | htpX | O | Belongs to the peptidase M48B family | ||
HIDONJMO_01379 | 1.8e-259 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HIDONJMO_01380 | 1.4e-249 | 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 | |
HIDONJMO_01381 | 3.1e-126 | L | PFAM Integrase catalytic region | |||
HIDONJMO_01382 | 2.3e-138 | sprD | D | Domain of Unknown Function (DUF1542) | ||
HIDONJMO_01383 | 6.5e-165 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
HIDONJMO_01384 | 1.4e-253 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
HIDONJMO_01385 | 2.8e-35 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HIDONJMO_01386 | 2.8e-232 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
HIDONJMO_01387 | 6.5e-295 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HIDONJMO_01389 | 2.2e-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 | |
HIDONJMO_01390 | 1.9e-211 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HIDONJMO_01391 | 3.2e-62 | L | Toxic component of a toxin-antitoxin (TA) module | |||
HIDONJMO_01392 | 6.8e-251 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
HIDONJMO_01393 | 4.7e-243 | codA | 3.5.4.1 | F | cytosine deaminase | |
HIDONJMO_01394 | 3.1e-147 | tesE | Q | hydratase | ||
HIDONJMO_01395 | 4e-113 | S | (CBS) domain | |||
HIDONJMO_01396 | 3.3e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HIDONJMO_01397 | 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 | ||
HIDONJMO_01398 | 8.1e-39 | yabO | J | S4 domain protein | ||
HIDONJMO_01399 | 3.3e-56 | divIC | D | Septum formation initiator | ||
HIDONJMO_01400 | 9.8e-67 | yabR | J | RNA binding | ||
HIDONJMO_01401 | 3.8e-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 | |
HIDONJMO_01402 | 1.5e-97 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HIDONJMO_01403 | 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 | ||
HIDONJMO_01404 | 1.4e-170 | 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 | ||
HIDONJMO_01405 | 1.1e-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 | ||
HIDONJMO_01406 | 6.1e-293 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HIDONJMO_01407 | 5.5e-280 | O | Arylsulfotransferase (ASST) | |||
HIDONJMO_01414 | 1.1e-130 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
HIDONJMO_01415 | 1.1e-136 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
HIDONJMO_01416 | 5.5e-142 | 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 | |
HIDONJMO_01417 | 8.8e-259 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
HIDONJMO_01418 | 1.9e-74 | 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 | |
HIDONJMO_01419 | 5.8e-74 | 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 | |
HIDONJMO_01420 | 2.6e-225 | 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 | |
HIDONJMO_01421 | 2.7e-129 | IQ | reductase | |||
HIDONJMO_01422 | 1.6e-158 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
HIDONJMO_01423 | 6.5e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HIDONJMO_01424 | 2.1e-177 | 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 | |
HIDONJMO_01425 | 4.2e-77 | marR | K | Transcriptional regulator, MarR family | ||
HIDONJMO_01426 | 6.6e-72 | 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 | |
HIDONJMO_01428 | 2.8e-199 | xerS | L | Belongs to the 'phage' integrase family | ||
HIDONJMO_01429 | 2.5e-145 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HIDONJMO_01430 | 2.2e-131 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HIDONJMO_01431 | 4.9e-164 | oppD | P | Belongs to the ABC transporter superfamily | ||
HIDONJMO_01432 | 3.8e-138 | P | Belongs to the ABC transporter superfamily | |||
HIDONJMO_01433 | 6.9e-159 | Q | Imidazolonepropionase and related amidohydrolases | |||
HIDONJMO_01434 | 8.3e-223 | dap2 | 3.4.19.1 | E | Prolyl oligopeptidase family | |
HIDONJMO_01435 | 2.4e-191 | Q | Imidazolonepropionase and related amidohydrolases | |||
HIDONJMO_01436 | 5.7e-218 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
HIDONJMO_01437 | 9.9e-42 | L | Transposase and inactivated derivatives | |||
HIDONJMO_01438 | 1.1e-150 | L | Integrase core domain | |||
HIDONJMO_01439 | 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) | |
HIDONJMO_01440 | 3e-34 | |||||
HIDONJMO_01441 | 2.5e-289 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HIDONJMO_01442 | 9.9e-191 | tdh | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
HIDONJMO_01443 | 2.6e-86 | ygfC | K | transcriptional regulator (TetR family) | ||
HIDONJMO_01444 | 2e-178 | hrtB | V | ABC transporter permease | ||
HIDONJMO_01445 | 1.8e-114 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
HIDONJMO_01446 | 0.0 | yhcA | V | ABC transporter, ATP-binding protein | ||
HIDONJMO_01447 | 1.6e-14 | |||||
HIDONJMO_01448 | 0.0 | L | PLD-like domain | |||
HIDONJMO_01449 | 3.7e-35 | higA | K | addiction module antidote protein HigA | ||
HIDONJMO_01450 | 6e-142 | pstS | P | T5orf172 | ||
HIDONJMO_01451 | 0.0 | yeeB | L | DEAD-like helicases superfamily | ||
HIDONJMO_01452 | 5.3e-88 | J | tRNA cytidylyltransferase activity | |||
HIDONJMO_01454 | 0.0 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
HIDONJMO_01455 | 6.6e-262 | S | Putative peptidoglycan binding domain | |||
HIDONJMO_01456 | 3.5e-109 | 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 | |
HIDONJMO_01457 | 2.2e-87 | |||||
HIDONJMO_01458 | 5.7e-244 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
HIDONJMO_01459 | 4.4e-214 | yttB | EGP | Major facilitator Superfamily | ||
HIDONJMO_01460 | 8.2e-103 | |||||
HIDONJMO_01461 | 3e-24 | |||||
HIDONJMO_01462 | 5.1e-173 | scrR | K | Transcriptional regulator, LacI family | ||
HIDONJMO_01463 | 2e-212 | acm2 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |
HIDONJMO_01465 | 7.6e-112 | lssY | 3.6.1.27 | I | Acid phosphatase homologues | |
HIDONJMO_01466 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
HIDONJMO_01467 | 2.5e-209 | clcA_2 | P | Chloride transporter, ClC family | ||
HIDONJMO_01468 | 5.1e-116 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
HIDONJMO_01469 | 2.4e-147 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HIDONJMO_01470 | 3.9e-134 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
HIDONJMO_01471 | 5.2e-50 | |||||
HIDONJMO_01472 | 0.0 | S | SEC-C Motif Domain Protein | |||
HIDONJMO_01473 | 2.1e-41 | ybaN | S | Protein of unknown function (DUF454) | ||
HIDONJMO_01474 | 9.1e-72 | S | Protein of unknown function (DUF3290) | |||
HIDONJMO_01475 | 6.2e-114 | yviA | S | Protein of unknown function (DUF421) | ||
HIDONJMO_01476 | 4.4e-163 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HIDONJMO_01477 | 1.3e-20 | |||||
HIDONJMO_01478 | 8.1e-90 | ntd | 2.4.2.6 | F | Nucleoside | |
HIDONJMO_01479 | 5.6e-155 | 3.1.3.102, 3.1.3.104 | S | hydrolase | ||
HIDONJMO_01480 | 1.6e-45 | yrvD | S | Pfam:DUF1049 | ||
HIDONJMO_01482 | 1.1e-35 | S | Phage derived protein Gp49-like (DUF891) | |||
HIDONJMO_01483 | 8.5e-20 | K | Helix-turn-helix XRE-family like proteins | |||
HIDONJMO_01484 | 1.7e-78 | I | alpha/beta hydrolase fold | |||
HIDONJMO_01485 | 1.1e-113 | frnE | Q | DSBA-like thioredoxin domain | ||
HIDONJMO_01486 | 2e-53 | |||||
HIDONJMO_01487 | 7.9e-188 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
HIDONJMO_01488 | 4e-28 | ltrA_1 | 2.7.7.49 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |
HIDONJMO_01489 | 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 | |
HIDONJMO_01490 | 3.2e-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 | |
HIDONJMO_01491 | 1.3e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
HIDONJMO_01492 | 2.2e-230 | 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 | ||
HIDONJMO_01493 | 3.7e-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 | ||
HIDONJMO_01494 | 1.6e-35 | |||||
HIDONJMO_01495 | 3.2e-101 | K | DNA-templated transcription, initiation | |||
HIDONJMO_01496 | 6.1e-29 | |||||
HIDONJMO_01497 | 6.2e-60 | L | PFAM transposase IS200-family protein | |||
HIDONJMO_01498 | 1.3e-229 | L | transposase, IS605 OrfB family | |||
HIDONJMO_01499 | 2e-40 | K | Transcriptional regulator, HxlR family | |||
HIDONJMO_01500 | 2.4e-165 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HIDONJMO_01501 | 1.4e-137 | epsB | M | biosynthesis protein | ||
HIDONJMO_01502 | 1.1e-119 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
HIDONJMO_01503 | 2e-51 | pglC | M | Bacterial sugar transferase | ||
HIDONJMO_01504 | 1.9e-172 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
HIDONJMO_01505 | 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 | |
HIDONJMO_01506 | 2e-115 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
HIDONJMO_01507 | 4.7e-114 | yjbH | Q | Thioredoxin | ||
HIDONJMO_01508 | 2.7e-263 | pipD | E | Dipeptidase | ||
HIDONJMO_01509 | 3e-203 | coiA | 3.6.4.12 | S | Competence protein | |
HIDONJMO_01510 | 2.7e-120 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HIDONJMO_01511 | 1.6e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
HIDONJMO_01512 | 1.8e-76 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
HIDONJMO_01513 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
HIDONJMO_01514 | 2.4e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
HIDONJMO_01515 | 3.9e-72 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
HIDONJMO_01516 | 1.5e-118 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
HIDONJMO_01517 | 2.2e-202 | ykiI | ||||
HIDONJMO_01518 | 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 | |
HIDONJMO_01519 | 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 | |
HIDONJMO_01520 | 5.1e-110 | K | Bacterial regulatory proteins, tetR family | |||
HIDONJMO_01521 | 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 | ||
HIDONJMO_01522 | 4.4e-77 | ctsR | K | Belongs to the CtsR family | ||
HIDONJMO_01523 | 1.2e-196 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
HIDONJMO_01524 | 1.3e-16 | S | Hydrolases of the alpha beta superfamily | |||
HIDONJMO_01525 | 1.5e-91 | S | Hydrolases of the alpha beta superfamily | |||
HIDONJMO_01531 | 4.3e-115 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HIDONJMO_01532 | 1.5e-275 | lysP | E | amino acid | ||
HIDONJMO_01533 | 3.5e-10 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
HIDONJMO_01534 | 2.7e-120 | lssY | 3.6.1.27 | I | phosphatase | |
HIDONJMO_01535 | 2.5e-80 | S | Threonine/Serine exporter, ThrE | |||
HIDONJMO_01536 | 3.6e-129 | thrE | S | Putative threonine/serine exporter | ||
HIDONJMO_01537 | 3.5e-31 | cspC | K | Cold shock protein | ||
HIDONJMO_01538 | 1.1e-124 | sirR | K | iron dependent repressor | ||
HIDONJMO_01539 | 2.6e-166 | czcD | P | cation diffusion facilitator family transporter | ||
HIDONJMO_01540 | 5e-117 | S | membrane | |||
HIDONJMO_01541 | 7.6e-110 | S | VIT family | |||
HIDONJMO_01542 | 5.5e-83 | usp1 | T | Belongs to the universal stress protein A family | ||
HIDONJMO_01543 | 5.3e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HIDONJMO_01544 | 2.2e-151 | glnH | ET | ABC transporter | ||
HIDONJMO_01545 | 4.2e-110 | gluC | P | ABC transporter permease | ||
HIDONJMO_01546 | 1.4e-108 | glnP | P | ABC transporter permease | ||
HIDONJMO_01547 | 1.1e-217 | S | CAAX protease self-immunity | |||
HIDONJMO_01548 | 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 | ||
HIDONJMO_01549 | 9.3e-56 | |||||
HIDONJMO_01550 | 1.8e-72 | merR | K | MerR HTH family regulatory protein | ||
HIDONJMO_01551 | 2.7e-269 | lmrB | EGP | Major facilitator Superfamily | ||
HIDONJMO_01552 | 5.6e-119 | S | Domain of unknown function (DUF4811) | |||
HIDONJMO_01553 | 4.6e-160 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HIDONJMO_01555 | 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 | |
HIDONJMO_01556 | 4e-104 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
HIDONJMO_01557 | 7.7e-188 | I | Alpha beta | |||
HIDONJMO_01558 | 8.5e-282 | emrY | EGP | Major facilitator Superfamily | ||
HIDONJMO_01559 | 2.8e-117 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
HIDONJMO_01560 | 2e-250 | yjjP | S | Putative threonine/serine exporter | ||
HIDONJMO_01561 | 1e-159 | mleR | K | LysR family | ||
HIDONJMO_01562 | 1.3e-252 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
HIDONJMO_01563 | 1.8e-267 | frdC | 1.3.5.4 | C | FAD binding domain | |
HIDONJMO_01564 | 4.7e-260 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
HIDONJMO_01565 | 2.2e-304 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
HIDONJMO_01566 | 1.9e-161 | mleR | K | LysR family | ||
HIDONJMO_01567 | 1e-110 | 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 | |
HIDONJMO_01568 | 1.1e-205 | adhA | 1.1.1.1 | C | Zinc-binding alcohol dehydrogenase family protein | |
HIDONJMO_01569 | 9.4e-295 | L | PFAM plasmid pRiA4b ORF-3 family protein | |||
HIDONJMO_01570 | 1.6e-168 | L | transposase, IS605 OrfB family | |||
HIDONJMO_01571 | 3.5e-263 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
HIDONJMO_01572 | 1.5e-25 | |||||
HIDONJMO_01573 | 3.2e-200 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
HIDONJMO_01574 | 3e-75 | |||||
HIDONJMO_01575 | 7.4e-228 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HIDONJMO_01576 | 4.8e-132 | ponA | V | Beta-lactamase enzyme family | ||
HIDONJMO_01577 | 1.7e-284 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
HIDONJMO_01578 | 5.3e-215 | uhpT | EGP | Major facilitator Superfamily | ||
HIDONJMO_01579 | 1.3e-254 | ytjP | 3.5.1.18 | E | Dipeptidase | |
HIDONJMO_01580 | 2.2e-274 | arcD | S | C4-dicarboxylate anaerobic carrier | ||
HIDONJMO_01581 | 5e-75 | osmC | O | OsmC-like protein | ||
HIDONJMO_01582 | 1.2e-175 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HIDONJMO_01583 | 6.1e-216 | patA | 2.6.1.1 | E | Aminotransferase | |
HIDONJMO_01584 | 7.8e-32 | |||||
HIDONJMO_01585 | 0.0 | clpL | O | associated with various cellular activities | ||
HIDONJMO_01586 | 5.1e-188 | ps461 | 3.5.1.104 | M | hydrolase, family 25 | |
HIDONJMO_01587 | 5.1e-56 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
HIDONJMO_01588 | 3.8e-34 | |||||
HIDONJMO_01592 | 3.4e-85 | S | Domain of unknown function (DUF2479) | |||
HIDONJMO_01594 | 6.7e-278 | pipD | E | Dipeptidase | ||
HIDONJMO_01595 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
HIDONJMO_01596 | 2.7e-25 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
HIDONJMO_01597 | 3.6e-290 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
HIDONJMO_01598 | 2.9e-82 | |||||
HIDONJMO_01599 | 1.6e-219 | norA | EGP | Major facilitator Superfamily | ||
HIDONJMO_01600 | 5.8e-40 | 1.3.5.4 | S | FMN binding | ||
HIDONJMO_01601 | 9.3e-118 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
HIDONJMO_01602 | 1e-265 | yfnA | E | amino acid | ||
HIDONJMO_01603 | 1.3e-254 | gabT | 2.6.1.19 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
HIDONJMO_01608 | 1.5e-17 | NU | Mycoplasma protein of unknown function, DUF285 | |||
HIDONJMO_01610 | 1.2e-157 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
HIDONJMO_01611 | 4.4e-88 | 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) | |
HIDONJMO_01612 | 1.2e-64 | O | Zinc-dependent metalloprotease | |||
HIDONJMO_01613 | 4.7e-111 | S | Membrane | |||
HIDONJMO_01614 | 5.1e-42 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
HIDONJMO_01615 | 1.2e-14 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HIDONJMO_01616 | 4e-27 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HIDONJMO_01617 | 1.9e-168 | arsB | 1.20.4.1 | P | Sodium Bile acid symporter family | |
HIDONJMO_01618 | 6.2e-35 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
HIDONJMO_01620 | 8.5e-65 | repB | L | Initiator Replication protein | ||
HIDONJMO_01621 | 5.6e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HIDONJMO_01622 | 4.5e-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 | ||
HIDONJMO_01623 | 1.9e-141 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HIDONJMO_01624 | 5.7e-141 | 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 | ||
HIDONJMO_01625 | 7.8e-152 | 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 | |
HIDONJMO_01626 | 3e-145 | ecfA1 | 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 | ||
HIDONJMO_01627 | 1.1e-160 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
HIDONJMO_01628 | 1.2e-113 | recT | L | RecT family | ||
HIDONJMO_01635 | 1.2e-11 | |||||
HIDONJMO_01636 | 3.4e-29 | 3.4.21.88 | K | Helix-turn-helix domain | ||
HIDONJMO_01637 | 0.0 | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | |||
HIDONJMO_01638 | 5.5e-158 | endA | V | DNA/RNA non-specific endonuclease | ||
HIDONJMO_01639 | 1e-254 | yifK | E | Amino acid permease | ||
HIDONJMO_01641 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
HIDONJMO_01642 | 8.4e-216 | N | Uncharacterized conserved protein (DUF2075) | |||
HIDONJMO_01643 | 2.3e-122 | S | SNARE associated Golgi protein | |||
HIDONJMO_01644 | 2e-98 | uvrA3 | L | excinuclease ABC, A subunit | ||
HIDONJMO_01645 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
HIDONJMO_01646 | 9.1e-56 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HIDONJMO_01647 | 1.2e-59 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HIDONJMO_01648 | 8.3e-69 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
HIDONJMO_01649 | 8.1e-143 | S | DUF218 domain | |||
HIDONJMO_01650 | 0.0 | ubiB | S | ABC1 family | ||
HIDONJMO_01651 | 2.5e-245 | yhdP | S | Transporter associated domain | ||
HIDONJMO_01652 | 1.1e-74 | copY | K | Copper transport repressor CopY TcrY | ||
HIDONJMO_01653 | 1.3e-244 | EGP | Major facilitator Superfamily | |||
HIDONJMO_01654 | 1e-73 | yeaL | S | UPF0756 membrane protein | ||
HIDONJMO_01655 | 5.6e-79 | yphH | S | Cupin domain | ||
HIDONJMO_01656 | 6.6e-69 | C | Flavodoxin | |||
HIDONJMO_01657 | 1.4e-37 | K | LysR substrate binding domain protein | |||
HIDONJMO_01658 | 1.7e-170 | 1.1.1.346 | C | Aldo keto reductase | ||
HIDONJMO_01659 | 2.1e-39 | gcvR | T | Belongs to the UPF0237 family | ||
HIDONJMO_01660 | 2.6e-239 | XK27_08635 | S | UPF0210 protein | ||
HIDONJMO_01661 | 1.5e-94 | K | Acetyltransferase (GNAT) domain | |||
HIDONJMO_01662 | 4.4e-160 | S | Alpha beta hydrolase | |||
HIDONJMO_01663 | 4.9e-159 | gspA | M | family 8 | ||
HIDONJMO_01664 | 1.3e-229 | L | transposase, IS605 OrfB family | |||
HIDONJMO_01665 | 9.5e-77 | tlpA2 | L | Transposase IS200 like | ||
HIDONJMO_01666 | 2.3e-116 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HIDONJMO_01667 | 2.1e-91 | |||||
HIDONJMO_01668 | 6.4e-162 | degV | S | EDD domain protein, DegV family | ||
HIDONJMO_01669 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
HIDONJMO_01670 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HIDONJMO_01671 | 8.1e-207 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
HIDONJMO_01672 | 3.8e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HIDONJMO_01673 | 2.9e-70 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HIDONJMO_01674 | 1.5e-65 | esbA | S | Family of unknown function (DUF5322) | ||
HIDONJMO_01675 | 3.4e-70 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
HIDONJMO_01676 | 5.6e-222 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HIDONJMO_01677 | 1.1e-83 | F | Belongs to the NrdI family | |||
HIDONJMO_01678 | 1.7e-44 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
HIDONJMO_01679 | 1.6e-105 | ypsA | S | Belongs to the UPF0398 family | ||
HIDONJMO_01680 | 4.4e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
HIDONJMO_01681 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
HIDONJMO_01682 | 2e-161 | EG | EamA-like transporter family | |||
HIDONJMO_01683 | 3e-125 | dnaD | L | DnaD domain protein | ||
HIDONJMO_01684 | 2.9e-85 | ypmB | S | Protein conserved in bacteria | ||
HIDONJMO_01685 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
HIDONJMO_01686 | 5.7e-172 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
HIDONJMO_01687 | 4.6e-169 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
HIDONJMO_01688 | 4.2e-214 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
HIDONJMO_01689 | 1.7e-193 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
HIDONJMO_01690 | 3.8e-87 | S | Protein of unknown function (DUF1440) | |||
HIDONJMO_01691 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
HIDONJMO_01692 | 4.2e-189 | galR | K | Periplasmic binding protein-like domain | ||
HIDONJMO_01693 | 1.9e-169 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
HIDONJMO_01695 | 6.1e-247 | mmuP | E | amino acid | ||
HIDONJMO_01696 | 8e-120 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
HIDONJMO_01697 | 9.3e-22 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
HIDONJMO_01698 | 7.3e-19 | |||||
HIDONJMO_01699 | 2.7e-70 | S | GyrI-like small molecule binding domain | |||
HIDONJMO_01700 | 6.4e-39 | S | GyrI-like small molecule binding domain | |||
HIDONJMO_01701 | 5e-122 | yhiD | S | MgtC family | ||
HIDONJMO_01702 | 3e-93 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HIDONJMO_01703 | 5.9e-191 | V | Beta-lactamase | |||
HIDONJMO_01704 | 2.2e-111 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
HIDONJMO_01705 | 6.7e-93 | dps | P | Belongs to the Dps family | ||
HIDONJMO_01706 | 7.9e-35 | copZ | C | Heavy-metal-associated domain | ||
HIDONJMO_01707 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
HIDONJMO_01709 | 9.1e-38 | K | Helix-turn-helix domain | |||
HIDONJMO_01710 | 1.6e-53 | S | Phage derived protein Gp49-like (DUF891) | |||
HIDONJMO_01711 | 1.3e-94 | L | Integrase | |||
HIDONJMO_01712 | 2.4e-36 | |||||
HIDONJMO_01715 | 7.3e-41 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
HIDONJMO_01716 | 5.4e-09 | S | Cytochrome B5 | |||
HIDONJMO_01717 | 7.8e-41 | S | Cytochrome B5 | |||
HIDONJMO_01718 | 6.7e-212 | yxjG_1 | E | methionine synthase, vitamin-B12 independent | ||
HIDONJMO_01720 | 2.3e-181 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HIDONJMO_01721 | 7.1e-230 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HIDONJMO_01722 | 1.3e-309 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
HIDONJMO_01723 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
HIDONJMO_01724 | 5.4e-202 | |||||
HIDONJMO_01725 | 1.1e-158 | spoU | 2.1.1.185 | J | Methyltransferase | |
HIDONJMO_01726 | 4.9e-224 | oxlT | P | Major Facilitator Superfamily | ||
HIDONJMO_01727 | 0.0 | pduC | 4.2.1.28 | Q | Dehydratase large subunit | |
HIDONJMO_01728 | 2.1e-108 | pduB | E | BMC | ||
HIDONJMO_01729 | 7.2e-35 | pduA_4 | CQ | BMC | ||
HIDONJMO_01730 | 1.5e-183 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HIDONJMO_01731 | 2.7e-39 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HIDONJMO_01732 | 2.5e-155 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HIDONJMO_01733 | 8.3e-265 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
HIDONJMO_01734 | 1.1e-90 | bioY | S | BioY family | ||
HIDONJMO_01735 | 1.5e-175 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HIDONJMO_01736 | 1.2e-183 | phoH | T | phosphate starvation-inducible protein PhoH | ||
HIDONJMO_01737 | 1.9e-83 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
HIDONJMO_01738 | 1.5e-62 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
HIDONJMO_01739 | 1.9e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HIDONJMO_01740 | 6.8e-147 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HIDONJMO_01741 | 2e-180 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HIDONJMO_01742 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
HIDONJMO_01743 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HIDONJMO_01744 | 2.8e-205 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
HIDONJMO_01745 | 1.2e-219 | patA | 2.6.1.1 | E | Aminotransferase | |
HIDONJMO_01746 | 9.6e-124 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
HIDONJMO_01747 | 3.1e-158 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
HIDONJMO_01748 | 7.3e-236 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
HIDONJMO_01749 | 3e-30 | S | Protein of unknown function (DUF2929) | |||
HIDONJMO_01750 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
HIDONJMO_01751 | 2.1e-271 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HIDONJMO_01752 | 2.3e-167 | cvfB | S | S1 domain | ||
HIDONJMO_01753 | 3.5e-163 | xerD | D | recombinase XerD | ||
HIDONJMO_01754 | 1.5e-64 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
HIDONJMO_01755 | 7.6e-138 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
HIDONJMO_01756 | 7.7e-106 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
HIDONJMO_01757 | 3.8e-128 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HIDONJMO_01758 | 4.5e-103 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
HIDONJMO_01759 | 9.1e-192 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
HIDONJMO_01760 | 1.5e-269 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HIDONJMO_01761 | 8.5e-14 | M | Lysin motif | |||
HIDONJMO_01762 | 3.4e-118 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
HIDONJMO_01763 | 2.5e-204 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
HIDONJMO_01764 | 7.2e-250 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HIDONJMO_01765 | 2.6e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
HIDONJMO_01766 | 1.5e-236 | S | Tetratricopeptide repeat protein | |||
HIDONJMO_01767 | 2.8e-224 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
HIDONJMO_01768 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
HIDONJMO_01769 | 1e-192 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
HIDONJMO_01770 | 1.9e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
HIDONJMO_01771 | 5.3e-113 | hlyIII | S | protein, hemolysin III | ||
HIDONJMO_01772 | 8.4e-151 | DegV | S | EDD domain protein, DegV family | ||
HIDONJMO_01773 | 9.5e-172 | ypmR | E | lipolytic protein G-D-S-L family | ||
HIDONJMO_01774 | 1.6e-108 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
HIDONJMO_01775 | 4.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
HIDONJMO_01776 | 4.6e-160 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
HIDONJMO_01777 | 1.2e-140 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HIDONJMO_01778 | 2.4e-161 | dprA | LU | DNA protecting protein DprA | ||
HIDONJMO_01779 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
HIDONJMO_01780 | 4.3e-166 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
HIDONJMO_01781 | 1.5e-107 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
HIDONJMO_01782 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
HIDONJMO_01783 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
HIDONJMO_01784 | 1.7e-84 | F | NUDIX domain | |||
HIDONJMO_01785 | 6.6e-173 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
HIDONJMO_01786 | 7.1e-83 | waaB | GT4 | M | Glycosyl transferases group 1 | |
HIDONJMO_01787 | 4.4e-21 | S | Psort location CytoplasmicMembrane, score | |||
HIDONJMO_01788 | 3.4e-48 | res | 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
HIDONJMO_01789 | 6e-15 | K | Helix-turn-helix domain | |||
HIDONJMO_01790 | 8.2e-14 | |||||
HIDONJMO_01791 | 3.7e-272 | E | ABC transporter, substratebinding protein | |||
HIDONJMO_01792 | 9.2e-217 | pduP | 1.2.1.87 | C | Aldehyde dehydrogenase family | |
HIDONJMO_01793 | 1.3e-202 | pduQ | C | Iron-containing alcohol dehydrogenase | ||
HIDONJMO_01794 | 1.7e-183 | S | Phosphotransferase system, EIIC | |||
HIDONJMO_01795 | 2.4e-98 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
HIDONJMO_01796 | 5.4e-67 | XK27_01125 | L | PFAM IS66 Orf2 family protein | ||
HIDONJMO_01798 | 1.1e-163 | yueF | S | AI-2E family transporter | ||
HIDONJMO_01799 | 2.9e-139 | csd1 | 3.5.1.28 | G | domain, Protein | |
HIDONJMO_01803 | 1.2e-293 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
HIDONJMO_01804 | 2.3e-162 | |||||
HIDONJMO_01805 | 2.9e-159 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
HIDONJMO_01806 | 2.8e-170 | S | AI-2E family transporter | |||
HIDONJMO_01807 | 4.2e-135 | XK27_07210 | 6.1.1.6 | S | B3 4 domain | |
HIDONJMO_01808 | 1.1e-77 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
HIDONJMO_01809 | 3.6e-91 | M1-874 | K | Domain of unknown function (DUF1836) | ||
HIDONJMO_01810 | 4.8e-88 | GM | epimerase | |||
HIDONJMO_01811 | 1.7e-154 | ypdB | V | (ABC) transporter | ||
HIDONJMO_01812 | 2.3e-240 | yhdP | S | Transporter associated domain | ||
HIDONJMO_01813 | 9.9e-85 | nrdI | F | Belongs to the NrdI family | ||
HIDONJMO_01814 | 3.2e-74 | S | 3-demethylubiquinone-9 3-methyltransferase | |||
HIDONJMO_01815 | 2e-192 | yeaN | P | Transporter, major facilitator family protein | ||
HIDONJMO_01816 | 2.2e-287 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HIDONJMO_01817 | 3.2e-275 | 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 | |
HIDONJMO_01818 | 1.2e-39 | |||||
HIDONJMO_01819 | 0.0 | lacS | G | Transporter | ||
HIDONJMO_01820 | 1.9e-41 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
HIDONJMO_01821 | 1.5e-09 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
HIDONJMO_01822 | 1.5e-80 | uspA | T | universal stress protein | ||
HIDONJMO_01823 | 1.5e-80 | K | AsnC family | |||
HIDONJMO_01824 | 1e-232 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
HIDONJMO_01825 | 9.5e-96 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
HIDONJMO_01826 | 2e-180 | galR | K | Transcriptional regulator | ||
HIDONJMO_01827 | 7.6e-285 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
HIDONJMO_01828 | 1.9e-225 | 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) | |
HIDONJMO_01829 | 8.6e-184 | celE | 3.2.1.4 | GH5,GH9 | E | GDSL-like Lipase/Acylhydrolase family |
HIDONJMO_01830 | 4e-147 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
HIDONJMO_01831 | 4.8e-93 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
HIDONJMO_01832 | 9.1e-36 | |||||
HIDONJMO_01833 | 5.9e-52 | |||||
HIDONJMO_01834 | 2.3e-204 | |||||
HIDONJMO_01835 | 2.2e-82 | 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 | ||
HIDONJMO_01836 | 8.9e-136 | pnuC | H | nicotinamide mononucleotide transporter | ||
HIDONJMO_01837 | 3.5e-157 | ytbE | 1.1.1.346 | S | Aldo keto reductase | |
HIDONJMO_01838 | 3.3e-132 | K | response regulator | |||
HIDONJMO_01839 | 3.8e-179 | T | PhoQ Sensor | |||
HIDONJMO_01840 | 2.6e-135 | macB2 | V | ABC transporter, ATP-binding protein | ||
HIDONJMO_01841 | 0.0 | ysaB | V | FtsX-like permease family | ||
HIDONJMO_01842 | 5.3e-158 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
HIDONJMO_01843 | 2.2e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HIDONJMO_01844 | 6.1e-54 | K | helix_turn_helix, mercury resistance | |||
HIDONJMO_01845 | 7.1e-286 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HIDONJMO_01846 | 1.6e-197 | EGP | Major facilitator Superfamily | |||
HIDONJMO_01847 | 2.1e-88 | ymdB | S | Macro domain protein | ||
HIDONJMO_01848 | 8.4e-111 | K | Helix-turn-helix domain | |||
HIDONJMO_01849 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HIDONJMO_01850 | 5.7e-46 | |||||
HIDONJMO_01851 | 4.2e-242 | S | Putative metallopeptidase domain | |||
HIDONJMO_01852 | 3e-204 | 3.1.3.1 | S | associated with various cellular activities | ||
HIDONJMO_01853 | 7.5e-120 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
HIDONJMO_01854 | 4.5e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
HIDONJMO_01856 | 5.4e-116 | yrkL | S | Flavodoxin-like fold | ||
HIDONJMO_01857 | 9.5e-55 | |||||
HIDONJMO_01858 | 2e-15 | S | Domain of unknown function (DUF4767) | |||
HIDONJMO_01859 | 2.6e-98 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HIDONJMO_01860 | 2.9e-27 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HIDONJMO_01861 | 6.9e-49 | |||||
HIDONJMO_01862 | 7.6e-205 | nrnB | S | DHHA1 domain | ||
HIDONJMO_01863 | 1.5e-228 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
HIDONJMO_01864 | 3.2e-248 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HIDONJMO_01865 | 9.9e-106 | NU | mannosyl-glycoprotein | |||
HIDONJMO_01866 | 2.3e-142 | S | Putative ABC-transporter type IV | |||
HIDONJMO_01867 | 7.8e-272 | S | ABC transporter, ATP-binding protein | |||
HIDONJMO_01868 | 7.4e-18 | |||||
HIDONJMO_01869 | 6.8e-50 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
HIDONJMO_01870 | 8.4e-42 | relB | L | RelB antitoxin | ||
HIDONJMO_01871 | 3.8e-94 | L | Integrase | |||
HIDONJMO_01873 | 2.8e-12 | |||||
HIDONJMO_01874 | 1.7e-15 | S | Bacteriophage holin family | |||
HIDONJMO_01878 | 3.7e-136 | azlC | E | AzlC protein | ||
HIDONJMO_01879 | 1.6e-52 | azlD | S | branched-chain amino acid | ||
HIDONJMO_01880 | 1e-10 | |||||
HIDONJMO_01881 | 6.5e-144 | S | Phage major capsid protein E | |||
HIDONJMO_01882 | 2.8e-35 | |||||
HIDONJMO_01885 | 4.5e-49 | |||||
HIDONJMO_01904 | 5.1e-94 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HIDONJMO_01905 | 5.3e-78 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
HIDONJMO_01906 | 3.3e-118 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
HIDONJMO_01907 | 5.6e-115 | rlpA | M | PFAM NLP P60 protein | ||
HIDONJMO_01908 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HIDONJMO_01909 | 6.6e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HIDONJMO_01910 | 2e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
HIDONJMO_01911 | 3.1e-92 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
HIDONJMO_01912 | 3.1e-144 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HIDONJMO_01913 | 7e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HIDONJMO_01914 | 5.9e-169 | 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 | ||
HIDONJMO_01915 | 8.7e-69 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HIDONJMO_01916 | 4.4e-231 | V | MatE | |||
HIDONJMO_01917 | 7.4e-267 | yjeM | E | Amino Acid | ||
HIDONJMO_01918 | 4.1e-278 | arlS | 2.7.13.3 | T | Histidine kinase | |
HIDONJMO_01919 | 1.5e-121 | K | response regulator | |||
HIDONJMO_01920 | 1.1e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HIDONJMO_01921 | 2.9e-99 | yceD | S | Uncharacterized ACR, COG1399 | ||
HIDONJMO_01922 | 2.1e-213 | ylbM | S | Belongs to the UPF0348 family | ||
HIDONJMO_01923 | 4.9e-139 | yqeM | Q | Methyltransferase | ||
HIDONJMO_01924 | 4.9e-60 | 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 | ||
HIDONJMO_01925 | 1e-113 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
HIDONJMO_01926 | 2.8e-122 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HIDONJMO_01927 | 1.9e-47 | yhbY | J | RNA-binding protein | ||
HIDONJMO_01928 | 2.1e-218 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
HIDONJMO_01929 | 1.8e-95 | yqeG | S | HAD phosphatase, family IIIA | ||
HIDONJMO_01930 | 1.6e-55 | 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 | ||
HIDONJMO_01931 | 2.3e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HIDONJMO_01932 | 3.7e-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 | ||
HIDONJMO_01933 | 1.1e-170 | dnaI | L | Primosomal protein DnaI | ||
HIDONJMO_01934 | 2.4e-200 | dnaB | L | replication initiation and membrane attachment | ||
HIDONJMO_01935 | 1.1e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HIDONJMO_01936 | 4.8e-100 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HIDONJMO_01937 | 7.4e-160 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
HIDONJMO_01938 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HIDONJMO_01939 | 4.1e-116 | yoaK | S | Protein of unknown function (DUF1275) | ||
HIDONJMO_01940 | 1.9e-119 | ybhL | S | Belongs to the BI1 family | ||
HIDONJMO_01941 | 1.9e-250 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HIDONJMO_01942 | 1.5e-35 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
HIDONJMO_01943 | 7e-48 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
HIDONJMO_01944 | 2.5e-118 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HIDONJMO_01945 | 1.7e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
HIDONJMO_01946 | 7.5e-58 | ytzB | S | Small secreted protein | ||
HIDONJMO_01947 | 9.4e-94 | cca | 2.7.7.19, 2.7.7.72 | J | Aminoglycoside-2''-adenylyltransferase | |
HIDONJMO_01948 | 7e-200 | L | transposition, DNA-mediated | |||
HIDONJMO_01949 | 3.4e-20 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
HIDONJMO_01950 | 6.8e-72 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
HIDONJMO_01951 | 8.8e-184 | iolS | C | Aldo keto reductase | ||
HIDONJMO_01952 | 1.2e-100 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
HIDONJMO_01953 | 5.1e-145 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
HIDONJMO_01954 | 2.8e-255 | 2.1.1.72, 3.1.21.3 | AA10,CBM73 | L | Belongs to the N(4) N(6)-methyltransferase family | |
HIDONJMO_01955 | 3.8e-66 | 2.1.1.72, 3.1.21.3 | AA10,CBM73 | L | Belongs to the N(4) N(6)-methyltransferase family | |
HIDONJMO_01956 | 7.7e-27 | S | YSIRK type signal peptide | |||
HIDONJMO_01957 | 1.1e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HIDONJMO_01958 | 5.1e-218 | ecsB | U | ABC transporter | ||
HIDONJMO_01959 | 4.3e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
HIDONJMO_01960 | 1.2e-76 | hit | FG | histidine triad | ||
HIDONJMO_01962 | 3.4e-129 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HIDONJMO_01963 | 0.0 | L | AAA domain | |||
HIDONJMO_01964 | 1.8e-220 | yhaO | L | Ser Thr phosphatase family protein | ||
HIDONJMO_01965 | 3.5e-40 | yheA | S | Belongs to the UPF0342 family | ||
HIDONJMO_01966 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HIDONJMO_01967 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)