ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KDBJKIBH_00001 | 1.2e-199 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
KDBJKIBH_00002 | 1e-40 | amd | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
KDBJKIBH_00003 | 9.9e-19 | S | Domain of unknown function (DUF4649) | |||
KDBJKIBH_00004 | 3.1e-72 | L | Transposase | |||
KDBJKIBH_00005 | 9e-23 | L | Transposase | |||
KDBJKIBH_00006 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
KDBJKIBH_00010 | 1.1e-32 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
KDBJKIBH_00011 | 2.1e-128 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
KDBJKIBH_00012 | 3.9e-250 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
KDBJKIBH_00013 | 3e-41 | yazA | L | endonuclease containing a URI domain | ||
KDBJKIBH_00014 | 1.2e-137 | yabB | 2.1.1.223 | L | Methyltransferase | |
KDBJKIBH_00015 | 2.9e-27 | L | Transposase | |||
KDBJKIBH_00016 | 4.1e-181 | L | Transposase | |||
KDBJKIBH_00017 | 8e-42 | nodB3 | G | polysaccharide deacetylase | ||
KDBJKIBH_00018 | 1.4e-79 | nodB3 | G | polysaccharide deacetylase | ||
KDBJKIBH_00019 | 1.3e-142 | plsC | 2.3.1.51 | I | Acyltransferase | |
KDBJKIBH_00020 | 1.1e-121 | L | Transposase | |||
KDBJKIBH_00021 | 1.2e-165 | L | integrase core domain | |||
KDBJKIBH_00023 | 8.9e-133 | agrA | KT | phosphorelay signal transduction system | ||
KDBJKIBH_00024 | 3.8e-238 | blpH | 2.7.13.3 | T | protein histidine kinase activity | |
KDBJKIBH_00026 | 9e-84 | mesE | M | Transport protein ComB | ||
KDBJKIBH_00027 | 1.2e-125 | mesE | M | Transport protein ComB | ||
KDBJKIBH_00028 | 1.8e-279 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
KDBJKIBH_00029 | 5.4e-33 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
KDBJKIBH_00031 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
KDBJKIBH_00032 | 2.4e-306 | mdlA | V | abc transporter atp-binding protein | ||
KDBJKIBH_00035 | 3.2e-92 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
KDBJKIBH_00036 | 4e-37 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
KDBJKIBH_00037 | 5.2e-11 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
KDBJKIBH_00038 | 7.3e-106 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
KDBJKIBH_00039 | 1e-64 | yutD | J | protein conserved in bacteria | ||
KDBJKIBH_00040 | 4.3e-269 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_00042 | 3.2e-221 | 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 | |
KDBJKIBH_00043 | 1.8e-184 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KDBJKIBH_00044 | 1.7e-105 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_00045 | 6e-59 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_00046 | 1.3e-146 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_00047 | 4.3e-47 | ftsL | D | cell division protein FtsL | ||
KDBJKIBH_00048 | 1.6e-191 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KDBJKIBH_00049 | 5.4e-30 | |||||
KDBJKIBH_00050 | 5.7e-37 | |||||
KDBJKIBH_00051 | 7.9e-55 | |||||
KDBJKIBH_00054 | 6.3e-31 | yhaI | J | Protein of unknown function (DUF805) | ||
KDBJKIBH_00055 | 9.3e-11 | D | nuclear chromosome segregation | |||
KDBJKIBH_00056 | 1.3e-224 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
KDBJKIBH_00057 | 4.4e-141 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
KDBJKIBH_00058 | 6.7e-134 | XK27_00765 | ||||
KDBJKIBH_00059 | 1e-134 | XK27_00765 | ||||
KDBJKIBH_00060 | 7.1e-130 | ecsA_2 | V | abc transporter atp-binding protein | ||
KDBJKIBH_00061 | 2.1e-101 | S | Protein of unknown function (DUF554) | |||
KDBJKIBH_00062 | 3.1e-10 | S | Protein of unknown function (DUF554) | |||
KDBJKIBH_00063 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
KDBJKIBH_00064 | 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 | |
KDBJKIBH_00065 | 1.6e-216 | 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 | |
KDBJKIBH_00066 | 3.6e-30 | liaI | S | membrane | ||
KDBJKIBH_00067 | 3.4e-66 | liaI | S | membrane | ||
KDBJKIBH_00068 | 5.4e-10 | XK27_02470 | K | LytTr DNA-binding domain protein | ||
KDBJKIBH_00069 | 8.5e-68 | KT | response to antibiotic | |||
KDBJKIBH_00070 | 1.8e-18 | KT | response to antibiotic | |||
KDBJKIBH_00071 | 3.1e-43 | yebC | M | Membrane | ||
KDBJKIBH_00072 | 9.5e-22 | yebC | M | Membrane | ||
KDBJKIBH_00073 | 2.9e-18 | yebC | M | Membrane | ||
KDBJKIBH_00074 | 5.1e-226 | XK27_03190 | 5.2.1.8 | S | hydrolases of the HAD superfamily | |
KDBJKIBH_00075 | 8.6e-09 | |||||
KDBJKIBH_00076 | 3.7e-73 | L | Transposase | |||
KDBJKIBH_00077 | 1.5e-171 | rny | D | Endoribonuclease that initiates mRNA decay | ||
KDBJKIBH_00078 | 1.7e-38 | L | transposase activity | |||
KDBJKIBH_00079 | 2.3e-156 | L | COG2801 Transposase and inactivated derivatives | |||
KDBJKIBH_00080 | 4.2e-109 | capM | K | Cell envelope-related transcriptional attenuator domain | ||
KDBJKIBH_00081 | 2.6e-142 | Dcc | 3.1.3.1, 3.1.3.5, 3.1.3.6, 3.1.4.16, 3.4.17.14, 3.6.1.45 | G | Phosphodiester glycosidase | |
KDBJKIBH_00083 | 1.1e-80 | S | Polysaccharide biosynthesis protein | |||
KDBJKIBH_00084 | 2.6e-50 | S | Polysaccharide biosynthesis protein | |||
KDBJKIBH_00085 | 2.8e-21 | S | Polysaccharide biosynthesis protein | |||
KDBJKIBH_00087 | 5.1e-09 | S | Glycosyl transferase, family 2 | |||
KDBJKIBH_00089 | 1.4e-82 | M | Glycosyl transferase, family 2 | |||
KDBJKIBH_00090 | 2.4e-31 | 2.4.1.52 | GT4 | V | Glycosyl transferase, family 2 | |
KDBJKIBH_00091 | 1.6e-28 | |||||
KDBJKIBH_00092 | 1.4e-60 | GT2 | S | Glycosyl transferase family 2 | ||
KDBJKIBH_00093 | 5e-28 | rfbF | GT2 | S | Glycosyl transferase family 2 | |
KDBJKIBH_00094 | 1.4e-29 | M | PFAM Glycosyl transferase, group 1 | |||
KDBJKIBH_00095 | 3.1e-131 | M | PFAM Glycosyl transferase, group 1 | |||
KDBJKIBH_00096 | 1.6e-84 | M | Glycosyl transferase 4-like | |||
KDBJKIBH_00097 | 3.5e-56 | rfbP | 2.7.8.6 | M | Bacterial sugar transferase | |
KDBJKIBH_00098 | 6.6e-115 | cpsD | D | COG0489 ATPases involved in chromosome partitioning | ||
KDBJKIBH_00099 | 4.1e-95 | cps4C | M | biosynthesis protein | ||
KDBJKIBH_00100 | 3e-110 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
KDBJKIBH_00101 | 3.5e-253 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KDBJKIBH_00102 | 3.4e-129 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
KDBJKIBH_00103 | 1.3e-23 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
KDBJKIBH_00104 | 2.6e-77 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
KDBJKIBH_00105 | 3.8e-09 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
KDBJKIBH_00106 | 3.9e-35 | clcA_2 | P | chloride | ||
KDBJKIBH_00107 | 8.7e-45 | clcA_2 | P | chloride channel | ||
KDBJKIBH_00108 | 1.2e-149 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
KDBJKIBH_00109 | 2.1e-46 | S | Protein of unknown function (DUF1697) | |||
KDBJKIBH_00110 | 1.9e-233 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
KDBJKIBH_00111 | 3e-50 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
KDBJKIBH_00112 | 8.6e-27 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
KDBJKIBH_00113 | 1.4e-12 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
KDBJKIBH_00115 | 2e-125 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
KDBJKIBH_00116 | 3.1e-33 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
KDBJKIBH_00117 | 9.3e-239 | L | Transposase | |||
KDBJKIBH_00118 | 5e-181 | EGP | Transmembrane secretion effector | |||
KDBJKIBH_00119 | 1.6e-94 | 6.3.2.2, 6.3.2.4 | M | ATP-grasp domain | ||
KDBJKIBH_00120 | 6.1e-119 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
KDBJKIBH_00123 | 8.7e-20 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KDBJKIBH_00124 | 4.4e-101 | L | nUDIX hydrolase | |||
KDBJKIBH_00125 | 3.2e-172 | 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) | |
KDBJKIBH_00126 | 1.3e-155 | K | Transcriptional activator, Rgg GadR MutR family | |||
KDBJKIBH_00127 | 4.6e-238 | L | Transposase | |||
KDBJKIBH_00128 | 9.9e-75 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
KDBJKIBH_00130 | 0.0 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
KDBJKIBH_00131 | 2.1e-199 | acoC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
KDBJKIBH_00132 | 2.1e-164 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
KDBJKIBH_00133 | 6e-185 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
KDBJKIBH_00134 | 1.9e-31 | P | membrane protein (DUF2207) | |||
KDBJKIBH_00135 | 1.2e-12 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_00136 | 5.7e-33 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_00137 | 2.4e-10 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_00138 | 5.2e-33 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
KDBJKIBH_00139 | 2.9e-33 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
KDBJKIBH_00140 | 7.8e-188 | 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 | |
KDBJKIBH_00141 | 0.0 | XK27_09800 | I | Acyltransferase | ||
KDBJKIBH_00142 | 1.7e-35 | XK27_09805 | S | MORN repeat protein | ||
KDBJKIBH_00143 | 1.8e-80 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
KDBJKIBH_00144 | 4.1e-250 | 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 | |
KDBJKIBH_00145 | 8.9e-95 | adk | 2.7.4.3 | F | topology modulation protein | |
KDBJKIBH_00147 | 5.7e-222 | L | Transposase | |||
KDBJKIBH_00149 | 3.4e-155 | Z012_04635 | K | sequence-specific DNA binding | ||
KDBJKIBH_00150 | 3.1e-196 | KLT | serine threonine protein kinase | |||
KDBJKIBH_00151 | 2e-169 | KLT | serine threonine protein kinase | |||
KDBJKIBH_00152 | 2.1e-280 | V | ABC transporter | |||
KDBJKIBH_00153 | 3.3e-13 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
KDBJKIBH_00154 | 1.3e-128 | Z012_04635 | K | sequence-specific DNA binding | ||
KDBJKIBH_00156 | 3.9e-102 | C | Radical SAM | |||
KDBJKIBH_00157 | 1.2e-117 | C | Radical SAM | |||
KDBJKIBH_00158 | 3.9e-287 | V | ABC transporter transmembrane region | |||
KDBJKIBH_00159 | 1.8e-126 | L | Replication initiation factor | |||
KDBJKIBH_00160 | 1.9e-18 | S | Domain of unknown function (DUF3173) | |||
KDBJKIBH_00161 | 7.7e-216 | int | L | Belongs to the 'phage' integrase family | ||
KDBJKIBH_00163 | 3.6e-64 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
KDBJKIBH_00164 | 7.2e-133 | parB | K | Belongs to the ParB family | ||
KDBJKIBH_00165 | 1.3e-257 | 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 | ||
KDBJKIBH_00166 | 9.1e-201 | 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 | |
KDBJKIBH_00167 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
KDBJKIBH_00168 | 8.6e-204 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
KDBJKIBH_00169 | 1.4e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
KDBJKIBH_00170 | 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 | ||
KDBJKIBH_00171 | 1.7e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
KDBJKIBH_00172 | 2.7e-61 | divIC | D | Septum formation initiator | ||
KDBJKIBH_00174 | 1.3e-240 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
KDBJKIBH_00175 | 1.4e-239 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
KDBJKIBH_00176 | 3.4e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KDBJKIBH_00177 | 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 | ||
KDBJKIBH_00178 | 7.1e-152 | L | Transposase | |||
KDBJKIBH_00179 | 1.4e-87 | L | Transposase | |||
KDBJKIBH_00180 | 4.2e-29 | L | transposition | |||
KDBJKIBH_00182 | 1.7e-87 | L | Integrase core domain protein | |||
KDBJKIBH_00183 | 4.1e-119 | desK | 2.7.13.3 | T | Histidine kinase | |
KDBJKIBH_00184 | 1e-97 | desR | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
KDBJKIBH_00185 | 9.6e-42 | S | (ABC) transporter | |||
KDBJKIBH_00186 | 4.3e-22 | S | (ABC) transporter | |||
KDBJKIBH_00187 | 1.8e-17 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KDBJKIBH_00188 | 1.2e-97 | S | transport system, permease component | |||
KDBJKIBH_00189 | 1.2e-33 | S | transport system, permease component | |||
KDBJKIBH_00190 | 9.2e-62 | S | ABC-2 family transporter protein | |||
KDBJKIBH_00191 | 5.7e-74 | S | ABC-2 family transporter protein | |||
KDBJKIBH_00192 | 6.5e-25 | |||||
KDBJKIBH_00193 | 5.3e-96 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
KDBJKIBH_00194 | 1.3e-40 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
KDBJKIBH_00195 | 1.2e-120 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
KDBJKIBH_00196 | 8.5e-301 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
KDBJKIBH_00197 | 5.4e-206 | S | Protein of unknown function (DUF917) | |||
KDBJKIBH_00198 | 1.5e-280 | hutH | 4.3.1.3 | E | Histidine ammonia-lyase | |
KDBJKIBH_00199 | 3e-111 | proWZ | P | ABC transporter (Permease | ||
KDBJKIBH_00200 | 2e-169 | proX | M | ABC transporter, substrate-binding protein, QAT family | ||
KDBJKIBH_00201 | 1.5e-138 | proV | E | abc transporter atp-binding protein | ||
KDBJKIBH_00202 | 3.6e-90 | proW | P | Binding-protein-dependent transport system inner membrane component | ||
KDBJKIBH_00203 | 8e-62 | bioY | S | biotin transmembrane transporter activity | ||
KDBJKIBH_00204 | 6.1e-100 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
KDBJKIBH_00205 | 3.1e-300 | 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 | ||
KDBJKIBH_00206 | 2.7e-238 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KDBJKIBH_00207 | 1.1e-30 | |||||
KDBJKIBH_00208 | 3e-13 | |||||
KDBJKIBH_00209 | 3e-193 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KDBJKIBH_00210 | 1e-153 | 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 | |
KDBJKIBH_00211 | 9.7e-109 | 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 | |
KDBJKIBH_00212 | 1.8e-234 | 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 | |
KDBJKIBH_00213 | 6e-177 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
KDBJKIBH_00214 | 6.5e-99 | pvaA | M | lytic transglycosylase activity | ||
KDBJKIBH_00215 | 0.0 | yfiB1 | V | abc transporter atp-binding protein | ||
KDBJKIBH_00216 | 8.9e-105 | XK27_10035 | V | abc transporter atp-binding protein | ||
KDBJKIBH_00217 | 1.2e-177 | XK27_10035 | V | abc transporter atp-binding protein | ||
KDBJKIBH_00218 | 3.8e-216 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
KDBJKIBH_00219 | 3.3e-74 | dltB | M | Membrane protein involved in D-alanine export | ||
KDBJKIBH_00220 | 4e-147 | dltB | M | Membrane protein involved in D-alanine export | ||
KDBJKIBH_00221 | 3.7e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
KDBJKIBH_00222 | 6.2e-222 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
KDBJKIBH_00223 | 7e-33 | L | Integrase core domain protein | |||
KDBJKIBH_00224 | 9.6e-32 | L | transposition | |||
KDBJKIBH_00225 | 2.4e-52 | L | transposition | |||
KDBJKIBH_00226 | 2.7e-258 | 3.6.3.8 | P | cation transport ATPase | ||
KDBJKIBH_00227 | 8.4e-213 | 3.6.3.8 | P | cation transport ATPase | ||
KDBJKIBH_00228 | 5.3e-83 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | component I | |
KDBJKIBH_00229 | 1.9e-184 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | component I | |
KDBJKIBH_00231 | 5.9e-13 | |||||
KDBJKIBH_00233 | 2.9e-48 | S | Virulence-associated protein E | |||
KDBJKIBH_00234 | 6.5e-24 | KL | Phage plasmid primase P4 family | |||
KDBJKIBH_00235 | 6.3e-44 | KL | Phage plasmid primase P4 family | |||
KDBJKIBH_00236 | 2.5e-182 | clpC | O | Belongs to the ClpA ClpB family | ||
KDBJKIBH_00237 | 6.9e-237 | clpC | O | Belongs to the ClpA ClpB family | ||
KDBJKIBH_00238 | 4.2e-124 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KDBJKIBH_00239 | 7.5e-18 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KDBJKIBH_00240 | 6.3e-17 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KDBJKIBH_00241 | 1.4e-231 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KDBJKIBH_00242 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
KDBJKIBH_00243 | 2e-143 | S | SseB protein N-terminal domain | |||
KDBJKIBH_00244 | 1.1e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
KDBJKIBH_00245 | 6.6e-259 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KDBJKIBH_00246 | 4.2e-68 | 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) | ||
KDBJKIBH_00250 | 4.8e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KDBJKIBH_00251 | 7e-92 | yacP | S | RNA-binding protein containing a PIN domain | ||
KDBJKIBH_00252 | 7.7e-132 | degV | S | DegV family | ||
KDBJKIBH_00254 | 2.5e-18 | K | helix-turn-helix | |||
KDBJKIBH_00255 | 3.6e-182 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
KDBJKIBH_00256 | 1.6e-48 | czcD | P | cation diffusion facilitator family transporter | ||
KDBJKIBH_00257 | 2.2e-34 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
KDBJKIBH_00258 | 4.6e-131 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
KDBJKIBH_00259 | 6.3e-194 | adhB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
KDBJKIBH_00260 | 6e-08 | S | Hydrolases of the alpha beta superfamily | |||
KDBJKIBH_00261 | 1.8e-16 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KDBJKIBH_00262 | 1.2e-79 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KDBJKIBH_00266 | 2.6e-143 | 2.4.2.3 | F | Phosphorylase superfamily | ||
KDBJKIBH_00267 | 4.1e-118 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
KDBJKIBH_00268 | 3.6e-14 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
KDBJKIBH_00269 | 1.2e-18 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
KDBJKIBH_00270 | 6.2e-22 | V | drug transmembrane transporter activity | |||
KDBJKIBH_00271 | 2.3e-73 | dinF | V | Mate efflux family protein | ||
KDBJKIBH_00272 | 6.3e-12 | dinF | V | Mate efflux family protein | ||
KDBJKIBH_00273 | 6e-310 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
KDBJKIBH_00274 | 5.7e-86 | L | Transposase | |||
KDBJKIBH_00275 | 4.1e-89 | L | Transposase | |||
KDBJKIBH_00276 | 6.8e-116 | HJ | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_00277 | 4.2e-10 | HJ | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_00278 | 1e-125 | gltT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
KDBJKIBH_00279 | 2.5e-13 | 2.3.1.82 | M | Acetyltransferase GNAT Family | ||
KDBJKIBH_00280 | 1.7e-53 | K | Putative DNA-binding domain | |||
KDBJKIBH_00281 | 4e-95 | L | PFAM Integrase, catalytic core | |||
KDBJKIBH_00282 | 1.2e-11 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
KDBJKIBH_00283 | 7.9e-19 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
KDBJKIBH_00284 | 2.3e-57 | 6.3.2.2 | H | ergothioneine biosynthetic process | ||
KDBJKIBH_00285 | 2.1e-80 | dcm | 2.1.1.37 | H | Cytosine-specific methyltransferase | |
KDBJKIBH_00286 | 1.7e-21 | |||||
KDBJKIBH_00287 | 1.7e-109 | K | Peptidase S24-like protein | |||
KDBJKIBH_00288 | 2.3e-127 | E | IrrE N-terminal-like domain | |||
KDBJKIBH_00290 | 2.9e-46 | K | Transcriptional | |||
KDBJKIBH_00291 | 1.7e-42 | |||||
KDBJKIBH_00292 | 8.6e-73 | |||||
KDBJKIBH_00293 | 2e-273 | ydcQ | D | Ftsk spoiiie family protein | ||
KDBJKIBH_00294 | 1e-221 | K | Replication initiation factor | |||
KDBJKIBH_00295 | 1.3e-32 | |||||
KDBJKIBH_00296 | 8.7e-88 | |||||
KDBJKIBH_00297 | 1.7e-158 | S | Conjugative transposon protein TcpC | |||
KDBJKIBH_00298 | 3.2e-33 | |||||
KDBJKIBH_00299 | 2.5e-68 | S | TcpE family | |||
KDBJKIBH_00300 | 0.0 | yddE | S | AAA-like domain | ||
KDBJKIBH_00301 | 3.2e-212 | |||||
KDBJKIBH_00302 | 4.4e-30 | |||||
KDBJKIBH_00303 | 6.2e-55 | isp2 | S | pathogenesis | ||
KDBJKIBH_00304 | 3.3e-110 | cps1C | S | Polysaccharide biosynthesis protein | ||
KDBJKIBH_00305 | 3.9e-100 | cps1C | S | Polysaccharide biosynthesis protein | ||
KDBJKIBH_00306 | 1e-108 | L | Transposase | |||
KDBJKIBH_00307 | 3.6e-107 | L | Transposase | |||
KDBJKIBH_00308 | 4.9e-166 | L | transposase, IS4 family | |||
KDBJKIBH_00309 | 2e-69 | V | VanZ like family | |||
KDBJKIBH_00310 | 8.9e-127 | tnp | L | DDE domain | ||
KDBJKIBH_00311 | 4.2e-154 | L | COG2801 Transposase and inactivated derivatives | |||
KDBJKIBH_00312 | 1.1e-113 | K | sequence-specific DNA binding | |||
KDBJKIBH_00313 | 2.7e-09 | C | Arylsulfatase regulator (Fe-S oxidoreductase) | |||
KDBJKIBH_00314 | 6e-143 | C | Arylsulfatase regulator (Fe-S oxidoreductase) | |||
KDBJKIBH_00315 | 5e-197 | V | (ABC) transporter | |||
KDBJKIBH_00316 | 1.7e-51 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
KDBJKIBH_00317 | 8e-277 | S | Protein of unknown function (DUF3114) | |||
KDBJKIBH_00319 | 1.9e-18 | tnp | L | DDE domain | ||
KDBJKIBH_00320 | 4.9e-78 | tnp | L | Transposase | ||
KDBJKIBH_00321 | 4.7e-27 | L | Transposase and inactivated derivatives, TnpA family | |||
KDBJKIBH_00323 | 7.9e-76 | gadC | E | Psort location CytoplasmicMembrane, score 10.00 | ||
KDBJKIBH_00324 | 9.5e-17 | asp | S | cog cog1302 | ||
KDBJKIBH_00325 | 7.1e-226 | norM | V | Mate efflux family protein | ||
KDBJKIBH_00326 | 1.6e-277 | thrC | 4.2.3.1 | E | Threonine synthase | |
KDBJKIBH_00327 | 1.1e-80 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KDBJKIBH_00328 | 1.6e-67 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KDBJKIBH_00329 | 2.4e-131 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KDBJKIBH_00330 | 1.4e-51 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KDBJKIBH_00331 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KDBJKIBH_00332 | 3.3e-39 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
KDBJKIBH_00333 | 5e-68 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
KDBJKIBH_00334 | 2.9e-65 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
KDBJKIBH_00335 | 7.2e-11 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
KDBJKIBH_00336 | 8.3e-14 | treB | 2.7.1.201 | G | pts system | |
KDBJKIBH_00337 | 5.8e-56 | treB | 2.7.1.201 | G | PTS System | |
KDBJKIBH_00338 | 5.8e-21 | treR | K | DNA-binding transcription factor activity | ||
KDBJKIBH_00339 | 1.5e-86 | treR | K | trehalose operon | ||
KDBJKIBH_00340 | 3.3e-95 | ywlG | S | Belongs to the UPF0340 family | ||
KDBJKIBH_00343 | 1.4e-38 | L | PFAM Integrase, catalytic core | |||
KDBJKIBH_00347 | 1.8e-19 | K | Cro/C1-type HTH DNA-binding domain | |||
KDBJKIBH_00348 | 4.8e-32 | xre | K | transcriptional | ||
KDBJKIBH_00349 | 4.5e-219 | sip | L | Belongs to the 'phage' integrase family | ||
KDBJKIBH_00351 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
KDBJKIBH_00352 | 1.3e-165 | metF | 1.5.1.20 | C | reductase | |
KDBJKIBH_00353 | 9e-107 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
KDBJKIBH_00354 | 2.6e-211 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
KDBJKIBH_00355 | 3.8e-94 | panT | S | ECF transporter, substrate-specific component | ||
KDBJKIBH_00356 | 4.3e-90 | 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 | |
KDBJKIBH_00357 | 1.2e-120 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
KDBJKIBH_00358 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
KDBJKIBH_00359 | 1.9e-89 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KDBJKIBH_00360 | 1.6e-40 | T | PhoQ Sensor | |||
KDBJKIBH_00361 | 1.1e-13 | T | PhoQ Sensor | |||
KDBJKIBH_00362 | 3.7e-111 | T | PhoQ Sensor | |||
KDBJKIBH_00363 | 2e-77 | L | integrase core domain | |||
KDBJKIBH_00364 | 5.2e-98 | L | DNA mismatch repair enzyme MutH | |||
KDBJKIBH_00367 | 1.4e-206 | S | AAA ATPase domain | |||
KDBJKIBH_00368 | 3.7e-46 | O | Protein conserved in bacteria | |||
KDBJKIBH_00369 | 5.8e-71 | |||||
KDBJKIBH_00370 | 5.6e-126 | O | AAA domain (Cdc48 subfamily) | |||
KDBJKIBH_00371 | 3.3e-23 | |||||
KDBJKIBH_00372 | 1.7e-221 | L | Transposase | |||
KDBJKIBH_00374 | 2.9e-35 | S | TraX protein | |||
KDBJKIBH_00375 | 1.1e-42 | S | TraX protein | |||
KDBJKIBH_00376 | 3.2e-95 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
KDBJKIBH_00377 | 1e-303 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
KDBJKIBH_00378 | 8.7e-248 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
KDBJKIBH_00379 | 4.6e-140 | 1.1.1.169 | H | Ketopantoate reductase | ||
KDBJKIBH_00380 | 2.2e-204 | 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) | |
KDBJKIBH_00381 | 3.4e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
KDBJKIBH_00382 | 2.6e-241 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
KDBJKIBH_00383 | 2.3e-130 | S | CHAP domain | |||
KDBJKIBH_00384 | 1.4e-33 | L | Integrase core domain protein | |||
KDBJKIBH_00385 | 1.2e-09 | L | Transposase | |||
KDBJKIBH_00386 | 3.7e-53 | L | transposase activity | |||
KDBJKIBH_00387 | 6.8e-292 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
KDBJKIBH_00388 | 7.4e-41 | 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 | |
KDBJKIBH_00389 | 3.4e-166 | K | transcriptional regulator (lysR family) | |||
KDBJKIBH_00390 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
KDBJKIBH_00395 | 2.6e-189 | phoH | T | phosphate starvation-inducible protein PhoH | ||
KDBJKIBH_00396 | 1.4e-61 | rlpA | M | LysM domain protein | ||
KDBJKIBH_00397 | 2.4e-89 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
KDBJKIBH_00398 | 8.2e-88 | mreD | M | Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins | ||
KDBJKIBH_00399 | 2.1e-138 | mreC | M | Involved in formation and maintenance of cell shape | ||
KDBJKIBH_00414 | 2.8e-24 | spd | F | DNA RNA non-specific endonuclease | ||
KDBJKIBH_00415 | 9.9e-143 | spd | F | DNA RNA non-specific endonuclease | ||
KDBJKIBH_00416 | 9.8e-45 | |||||
KDBJKIBH_00417 | 1e-28 | |||||
KDBJKIBH_00419 | 1.8e-135 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
KDBJKIBH_00420 | 1.4e-271 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KDBJKIBH_00421 | 0.0 | hsdR | 3.1.21.3 | V | Type I restriction enzyme R protein N terminus (HSDR_N) | |
KDBJKIBH_00422 | 1.5e-89 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KDBJKIBH_00423 | 6.9e-19 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KDBJKIBH_00424 | 5.5e-47 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
KDBJKIBH_00425 | 1.6e-21 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
KDBJKIBH_00426 | 1.4e-23 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
KDBJKIBH_00427 | 6.1e-114 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
KDBJKIBH_00428 | 2.7e-27 | P | Hemerythrin HHE cation binding domain protein | |||
KDBJKIBH_00429 | 4.5e-145 | XK27_00880 | 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
KDBJKIBH_00430 | 1.3e-18 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KDBJKIBH_00431 | 2.5e-22 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KDBJKIBH_00432 | 1.2e-114 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase | |
KDBJKIBH_00433 | 7.5e-174 | S | hydrolase | |||
KDBJKIBH_00434 | 5.9e-16 | |||||
KDBJKIBH_00436 | 3.8e-43 | M | LysM domain | |||
KDBJKIBH_00437 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KDBJKIBH_00440 | 1.2e-48 | yegS | 2.7.1.107 | I | Diacylglycerol kinase | |
KDBJKIBH_00441 | 2.4e-50 | yegS | 2.7.1.107 | I | lipid kinase activity | |
KDBJKIBH_00442 | 8.5e-97 | S | Hydrophobic domain protein | |||
KDBJKIBH_00444 | 7.4e-28 | S | Membrane | |||
KDBJKIBH_00445 | 1.4e-101 | |||||
KDBJKIBH_00446 | 2.3e-23 | S | Small integral membrane protein | |||
KDBJKIBH_00447 | 1.1e-85 | M | Protein conserved in bacteria | |||
KDBJKIBH_00448 | 1.1e-11 | K | CsbD-like | |||
KDBJKIBH_00449 | 2.7e-97 | nudL | L | hydrolase | ||
KDBJKIBH_00450 | 5.5e-08 | nudL | L | hydrolase | ||
KDBJKIBH_00451 | 4e-19 | K | negative regulation of transcription, DNA-templated | |||
KDBJKIBH_00452 | 1.7e-23 | K | negative regulation of transcription, DNA-templated | |||
KDBJKIBH_00454 | 1.2e-18 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
KDBJKIBH_00455 | 2.4e-108 | S | Putative adhesin | |||
KDBJKIBH_00456 | 2.6e-135 | XK27_06930 | V | domain protein | ||
KDBJKIBH_00457 | 1.6e-64 | XK27_06935 | K | transcriptional regulator | ||
KDBJKIBH_00458 | 5.2e-42 | ypaA | S | membrane | ||
KDBJKIBH_00459 | 5.6e-23 | ycbB | S | Glycosyl transferase family 2 | ||
KDBJKIBH_00461 | 1.4e-85 | amrA | S | polysaccharide biosynthetic process | ||
KDBJKIBH_00462 | 8.6e-123 | amrA | S | polysaccharide biosynthetic process | ||
KDBJKIBH_00463 | 1.4e-184 | tagF | 2.7.8.12 | M | Glycosyl transferase, family 2 | |
KDBJKIBH_00464 | 1.3e-226 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
KDBJKIBH_00465 | 6.4e-82 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
KDBJKIBH_00466 | 1e-81 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
KDBJKIBH_00467 | 2.8e-143 | rgpC | GM | Transport permease protein | ||
KDBJKIBH_00468 | 1.1e-206 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
KDBJKIBH_00469 | 8.2e-196 | rgpEc | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
KDBJKIBH_00470 | 0.0 | rgpF | M | Rhamnan synthesis protein F | ||
KDBJKIBH_00471 | 1.1e-119 | radC | E | Belongs to the UPF0758 family | ||
KDBJKIBH_00472 | 1.8e-130 | puuD | T | peptidase C26 | ||
KDBJKIBH_00473 | 1.7e-117 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
KDBJKIBH_00474 | 3.1e-59 | XK27_04120 | S | Putative amino acid metabolism | ||
KDBJKIBH_00475 | 3.2e-206 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
KDBJKIBH_00476 | 1.4e-47 | 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) | |
KDBJKIBH_00477 | 2.7e-143 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
KDBJKIBH_00478 | 1.4e-192 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
KDBJKIBH_00480 | 2.7e-50 | U | protein secretion | |||
KDBJKIBH_00483 | 2e-118 | 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 | |
KDBJKIBH_00484 | 6.4e-17 | |||||
KDBJKIBH_00485 | 1e-96 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
KDBJKIBH_00486 | 1.3e-165 | 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 | |
KDBJKIBH_00487 | 3e-75 | 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 | |
KDBJKIBH_00489 | 9.9e-191 | 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) | |
KDBJKIBH_00490 | 1.6e-177 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases N terminal domain | |
KDBJKIBH_00491 | 6e-174 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
KDBJKIBH_00492 | 5.1e-143 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
KDBJKIBH_00493 | 2e-94 | GBS0088 | J | protein conserved in bacteria | ||
KDBJKIBH_00494 | 1.8e-248 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
KDBJKIBH_00495 | 1.6e-133 | lacS | G | transporter | ||
KDBJKIBH_00496 | 4.9e-185 | lacS | G | transporter | ||
KDBJKIBH_00497 | 1.2e-188 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
KDBJKIBH_00498 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
KDBJKIBH_00499 | 1.7e-229 | 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 | ||
KDBJKIBH_00500 | 3.1e-171 | sbcC | L | ATPase involved in DNA repair | ||
KDBJKIBH_00501 | 3.1e-274 | sbcC | L | ATPase involved in DNA repair | ||
KDBJKIBH_00502 | 1.4e-20 | |||||
KDBJKIBH_00503 | 0.0 | M | family 8 | |||
KDBJKIBH_00504 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KDBJKIBH_00505 | 1.7e-259 | pepC | 3.4.22.40 | E | aminopeptidase | |
KDBJKIBH_00506 | 5.3e-59 | yhaI | L | Membrane | ||
KDBJKIBH_00507 | 4.5e-146 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
KDBJKIBH_00508 | 1.9e-275 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
KDBJKIBH_00509 | 2.9e-142 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
KDBJKIBH_00510 | 8.2e-88 | S | thiolester hydrolase activity | |||
KDBJKIBH_00511 | 3.8e-40 | K | transcriptional | |||
KDBJKIBH_00513 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KDBJKIBH_00514 | 5.6e-138 | glcR | K | transcriptional regulator (DeoR family) | ||
KDBJKIBH_00515 | 1.1e-34 | cof | Q | phosphatase activity | ||
KDBJKIBH_00516 | 2e-55 | cof | Q | phosphatase activity | ||
KDBJKIBH_00517 | 3.2e-44 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
KDBJKIBH_00518 | 6.6e-61 | EGP | Major facilitator Superfamily | |||
KDBJKIBH_00519 | 1.5e-118 | speB | 3.5.3.11 | E | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines | |
KDBJKIBH_00520 | 3.3e-106 | pqqE | C | radical SAM domain protein | ||
KDBJKIBH_00521 | 1.6e-96 | pqqE | C | radical SAM domain protein | ||
KDBJKIBH_00524 | 6.1e-157 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
KDBJKIBH_00525 | 1.1e-53 | K | peptidyl-tyrosine sulfation | |||
KDBJKIBH_00529 | 4e-190 | 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 | ||
KDBJKIBH_00530 | 3.8e-134 | 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 | ||
KDBJKIBH_00531 | 9.1e-46 | IQ | Acetoin reductase | |||
KDBJKIBH_00532 | 4.9e-49 | IQ | Acetoin reductase | |||
KDBJKIBH_00533 | 1e-47 | pspE | P | 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 | ||
KDBJKIBH_00534 | 1.7e-75 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
KDBJKIBH_00535 | 1.3e-153 | XK27_05470 | E | Methionine synthase | ||
KDBJKIBH_00536 | 6.6e-259 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
KDBJKIBH_00537 | 3.1e-162 | T | PhoQ Sensor | |||
KDBJKIBH_00538 | 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 | |
KDBJKIBH_00539 | 1.3e-113 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KDBJKIBH_00540 | 1.9e-30 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KDBJKIBH_00541 | 8.8e-81 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KDBJKIBH_00542 | 3.5e-25 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
KDBJKIBH_00543 | 1e-93 | cvpA | S | toxin biosynthetic process | ||
KDBJKIBH_00544 | 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 | ||
KDBJKIBH_00545 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
KDBJKIBH_00552 | 2.4e-104 | mutY | L | A G-specific adenine glycosylase | ||
KDBJKIBH_00553 | 2.1e-82 | mutY | L | A G-specific adenine glycosylase | ||
KDBJKIBH_00554 | 1.2e-44 | glcU | U | Glucose uptake | ||
KDBJKIBH_00555 | 1.3e-76 | glcU | U | Glucose uptake | ||
KDBJKIBH_00556 | 3.6e-114 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KDBJKIBH_00557 | 1.6e-57 | hsdS | 2.1.1.72, 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
KDBJKIBH_00558 | 4.1e-147 | L | Transposase | |||
KDBJKIBH_00559 | 5.3e-53 | L | Transposase | |||
KDBJKIBH_00560 | 1.3e-97 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
KDBJKIBH_00561 | 2.7e-219 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
KDBJKIBH_00562 | 5.1e-170 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
KDBJKIBH_00563 | 3.1e-105 | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | ||
KDBJKIBH_00564 | 9.1e-53 | L | Transposase | |||
KDBJKIBH_00565 | 1.2e-39 | L | Transposase, Mutator family | |||
KDBJKIBH_00566 | 2.7e-42 | L | Transposase | |||
KDBJKIBH_00567 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
KDBJKIBH_00568 | 3.6e-224 | L | Transposase, Mutator family | |||
KDBJKIBH_00569 | 1e-75 | 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 | ||
KDBJKIBH_00570 | 9.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
KDBJKIBH_00571 | 4.1e-36 | K | sequence-specific DNA binding | |||
KDBJKIBH_00573 | 6.8e-78 | S | Lantibiotic dehydratase, C terminus | |||
KDBJKIBH_00574 | 0.0 | S | Lantibiotic dehydratase, C terminus | |||
KDBJKIBH_00575 | 3.6e-230 | spaC2 | V | Lanthionine synthetase C family protein | ||
KDBJKIBH_00576 | 1.1e-180 | EGP | Major facilitator Superfamily | |||
KDBJKIBH_00577 | 4.5e-119 | |||||
KDBJKIBH_00579 | 1.9e-26 | isp2 | S | pathogenesis | ||
KDBJKIBH_00580 | 5.7e-91 | tnp | L | Transposase | ||
KDBJKIBH_00581 | 1.8e-153 | capA | M | Bacterial capsule synthesis protein | ||
KDBJKIBH_00582 | 3.7e-57 | capA | M | Bacterial capsule synthesis protein | ||
KDBJKIBH_00583 | 4.9e-25 | gcvR | T | UPF0237 protein | ||
KDBJKIBH_00584 | 5e-61 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
KDBJKIBH_00585 | 1.2e-92 | lytE | M | LysM domain protein | ||
KDBJKIBH_00586 | 1.9e-101 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KDBJKIBH_00587 | 2.1e-26 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KDBJKIBH_00588 | 5.2e-153 | 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 | |
KDBJKIBH_00589 | 1.5e-152 | 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 | ||
KDBJKIBH_00590 | 3.1e-90 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KDBJKIBH_00591 | 4.8e-138 | ymfM | S | sequence-specific DNA binding | ||
KDBJKIBH_00592 | 7.7e-241 | ymfH | S | Peptidase M16 | ||
KDBJKIBH_00593 | 6.9e-234 | ymfF | S | Peptidase M16 | ||
KDBJKIBH_00594 | 1.6e-45 | yaaA | S | S4 domain protein YaaA | ||
KDBJKIBH_00595 | 5.9e-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 | ||
KDBJKIBH_00596 | 2.6e-32 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
KDBJKIBH_00597 | 1.6e-233 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
KDBJKIBH_00598 | 2.9e-117 | 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 | ||
KDBJKIBH_00599 | 1e-84 | L | Integrase core domain protein | |||
KDBJKIBH_00600 | 1.6e-77 | 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 | ||
KDBJKIBH_00601 | 3.5e-25 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
KDBJKIBH_00602 | 7.7e-153 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
KDBJKIBH_00603 | 1.2e-50 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
KDBJKIBH_00604 | 8.7e-81 | XK27_09675 | K | -acetyltransferase | ||
KDBJKIBH_00605 | 1.5e-255 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
KDBJKIBH_00606 | 3.1e-21 | |||||
KDBJKIBH_00607 | 0.0 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
KDBJKIBH_00608 | 7.7e-298 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
KDBJKIBH_00609 | 2.6e-80 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
KDBJKIBH_00610 | 1.1e-127 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
KDBJKIBH_00611 | 5.4e-71 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
KDBJKIBH_00612 | 1.3e-64 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
KDBJKIBH_00613 | 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) | |
KDBJKIBH_00614 | 1.7e-183 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
KDBJKIBH_00615 | 1.5e-61 | 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 | |
KDBJKIBH_00616 | 1.1e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
KDBJKIBH_00617 | 1.9e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
KDBJKIBH_00618 | 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 | ||
KDBJKIBH_00620 | 1.9e-188 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
KDBJKIBH_00621 | 4.1e-172 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
KDBJKIBH_00622 | 4.3e-15 | scrA | 2.7.1.208, 2.7.1.211 | G | pts system | |
KDBJKIBH_00623 | 6.3e-130 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KDBJKIBH_00624 | 1.6e-163 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KDBJKIBH_00625 | 4.6e-73 | L | Transposase | |||
KDBJKIBH_00626 | 0.0 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
KDBJKIBH_00627 | 6.8e-84 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
KDBJKIBH_00628 | 2.8e-17 | V | (ABC) transporter | |||
KDBJKIBH_00629 | 2.2e-13 | V | abc transporter atp-binding protein | |||
KDBJKIBH_00630 | 1.2e-36 | V | abc transporter atp-binding protein | |||
KDBJKIBH_00631 | 2.1e-18 | rtxA | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
KDBJKIBH_00632 | 2.8e-31 | zmpB | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
KDBJKIBH_00633 | 3.8e-193 | M | translation initiation factor activity | |||
KDBJKIBH_00634 | 1.2e-25 | L | transposition | |||
KDBJKIBH_00635 | 7.1e-09 | L | Integrase core domain protein | |||
KDBJKIBH_00637 | 2.7e-163 | galR | K | Transcriptional regulator | ||
KDBJKIBH_00638 | 3.8e-218 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
KDBJKIBH_00639 | 2.6e-209 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
KDBJKIBH_00640 | 4.7e-45 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
KDBJKIBH_00641 | 8.4e-131 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KDBJKIBH_00642 | 9.2e-49 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KDBJKIBH_00643 | 1.1e-100 | yvgN | C | reductase | ||
KDBJKIBH_00644 | 5.8e-32 | yvgN | C | reductase | ||
KDBJKIBH_00646 | 1.5e-33 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
KDBJKIBH_00647 | 6.5e-84 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
KDBJKIBH_00648 | 3.8e-186 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
KDBJKIBH_00649 | 9.5e-144 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
KDBJKIBH_00650 | 1.4e-234 | sufD | O | assembly protein SufD | ||
KDBJKIBH_00651 | 3.4e-65 | 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 | |
KDBJKIBH_00652 | 7.2e-152 | 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 | |
KDBJKIBH_00653 | 1.1e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
KDBJKIBH_00654 | 2.2e-273 | sufB | O | assembly protein SufB | ||
KDBJKIBH_00655 | 2.7e-18 | oppA | E | ABC transporter substrate-binding protein | ||
KDBJKIBH_00656 | 1.1e-138 | oppA | E | ABC transporter substrate-binding protein | ||
KDBJKIBH_00657 | 8.5e-28 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KDBJKIBH_00658 | 6.3e-47 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KDBJKIBH_00659 | 6.5e-58 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KDBJKIBH_00660 | 8e-28 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_00661 | 5.5e-32 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_00662 | 2.8e-67 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_00663 | 1.4e-43 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_00664 | 1.5e-63 | oppF | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_00665 | 3.1e-87 | oppF | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_00666 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
KDBJKIBH_00667 | 3e-104 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
KDBJKIBH_00668 | 6.3e-171 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
KDBJKIBH_00669 | 4e-190 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
KDBJKIBH_00670 | 3.2e-281 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
KDBJKIBH_00671 | 6.8e-190 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
KDBJKIBH_00672 | 1.8e-50 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
KDBJKIBH_00673 | 4e-63 | 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 | |
KDBJKIBH_00674 | 3.2e-22 | 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 | |
KDBJKIBH_00675 | 3.7e-100 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
KDBJKIBH_00676 | 6.9e-26 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase activity | |
KDBJKIBH_00677 | 2.1e-82 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
KDBJKIBH_00678 | 5.6e-16 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
KDBJKIBH_00679 | 1.1e-172 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
KDBJKIBH_00680 | 2.1e-30 | rpsT | J | rRNA binding | ||
KDBJKIBH_00681 | 3.7e-15 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
KDBJKIBH_00682 | 1.1e-63 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
KDBJKIBH_00683 | 6.6e-279 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
KDBJKIBH_00684 | 1.3e-221 | L | Transposase | |||
KDBJKIBH_00686 | 7.6e-98 | |||||
KDBJKIBH_00688 | 1.3e-10 | |||||
KDBJKIBH_00689 | 1e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
KDBJKIBH_00690 | 1.5e-132 | ecsA | V | abc transporter atp-binding protein | ||
KDBJKIBH_00691 | 3.5e-152 | ecsB | U | ABC transporter | ||
KDBJKIBH_00692 | 9.8e-140 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
KDBJKIBH_00693 | 3.1e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KDBJKIBH_00695 | 5.7e-169 | ytfP | S | Flavoprotein | ||
KDBJKIBH_00696 | 1.1e-22 | ytfP | S | Flavoprotein | ||
KDBJKIBH_00697 | 9.5e-127 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KDBJKIBH_00698 | 4.6e-31 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KDBJKIBH_00699 | 3e-75 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KDBJKIBH_00700 | 1.1e-90 | trkA | P | Potassium transporter peripheral membrane component | ||
KDBJKIBH_00701 | 1.2e-53 | trkH | P | Cation transport protein | ||
KDBJKIBH_00702 | 6.7e-179 | trkH | P | Cation transport protein | ||
KDBJKIBH_00703 | 4.3e-42 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
KDBJKIBH_00704 | 4.6e-140 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
KDBJKIBH_00705 | 4.3e-98 | 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 | ||
KDBJKIBH_00706 | 2e-121 | 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 | ||
KDBJKIBH_00707 | 7.5e-138 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
KDBJKIBH_00708 | 1e-84 | ykuL | S | CBS domain | ||
KDBJKIBH_00709 | 1e-98 | XK27_09740 | S | Phosphoesterase | ||
KDBJKIBH_00710 | 2.1e-185 | 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 | |
KDBJKIBH_00711 | 2.1e-100 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
KDBJKIBH_00712 | 3.2e-37 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
KDBJKIBH_00713 | 9.2e-78 | K | transcriptional regulator | |||
KDBJKIBH_00714 | 9.6e-244 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
KDBJKIBH_00717 | 8.8e-98 | ybhL | S | Belongs to the BI1 family | ||
KDBJKIBH_00718 | 2.8e-69 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
KDBJKIBH_00719 | 1.4e-133 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
KDBJKIBH_00720 | 2.1e-25 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
KDBJKIBH_00721 | 5.3e-234 | femA | 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
KDBJKIBH_00723 | 5.2e-38 | yvdD | 3.2.2.10 | L | Belongs to the LOG family | |
KDBJKIBH_00724 | 1.2e-22 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
KDBJKIBH_00725 | 3.9e-57 | 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 | ||
KDBJKIBH_00726 | 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 | ||
KDBJKIBH_00727 | 2e-46 | ylxQ | J | ribosomal protein | ||
KDBJKIBH_00728 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
KDBJKIBH_00729 | 5.3e-204 | nusA | K | Participates in both transcription termination and antitermination | ||
KDBJKIBH_00730 | 1.5e-74 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
KDBJKIBH_00731 | 3.1e-22 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
KDBJKIBH_00732 | 5.8e-121 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
KDBJKIBH_00733 | 1.9e-36 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
KDBJKIBH_00734 | 7e-56 | nrdD_1 | 1.1.98.6, 1.17.4.1 | F | Ribonucleoside-triphosphate reductase | |
KDBJKIBH_00737 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KDBJKIBH_00738 | 6.4e-93 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
KDBJKIBH_00739 | 3.3e-197 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
KDBJKIBH_00740 | 5.3e-44 | smc | D | Required for chromosome condensation and partitioning | ||
KDBJKIBH_00741 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
KDBJKIBH_00742 | 2.6e-19 | 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 | |
KDBJKIBH_00743 | 1.4e-87 | 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 | |
KDBJKIBH_00744 | 3e-125 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
KDBJKIBH_00745 | 5.3e-217 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
KDBJKIBH_00749 | 1.9e-205 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
KDBJKIBH_00750 | 3.2e-112 | rmlC | 1.1.1.133, 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 | |
KDBJKIBH_00751 | 1.6e-160 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
KDBJKIBH_00752 | 5e-31 | yurR | 1.4.5.1 | E | oxidoreductase | |
KDBJKIBH_00753 | 6.7e-167 | yurR | 1.4.5.1 | E | oxidoreductase | |
KDBJKIBH_00754 | 3.5e-101 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
KDBJKIBH_00755 | 2.4e-22 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
KDBJKIBH_00756 | 8.8e-46 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
KDBJKIBH_00758 | 2e-47 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
KDBJKIBH_00759 | 8.2e-112 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
KDBJKIBH_00760 | 6.9e-28 | gtrA | S | GtrA-like protein | ||
KDBJKIBH_00761 | 2.7e-183 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KDBJKIBH_00762 | 8.2e-43 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
KDBJKIBH_00763 | 9.1e-30 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
KDBJKIBH_00764 | 4.4e-65 | ycdB | P | peroxidase | ||
KDBJKIBH_00765 | 3.5e-117 | ycdB | P | peroxidase | ||
KDBJKIBH_00766 | 1.7e-299 | ywbL | P | COG0672 High-affinity Fe2 Pb2 permease | ||
KDBJKIBH_00767 | 1.3e-120 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
KDBJKIBH_00768 | 4.6e-25 | tatA | U | protein secretion | ||
KDBJKIBH_00769 | 4e-111 | malF | P | ABC transporter (Permease | ||
KDBJKIBH_00770 | 8.5e-50 | malX | G | maltose binding | ||
KDBJKIBH_00771 | 4.5e-17 | malX | G | maltose binding | ||
KDBJKIBH_00772 | 2e-19 | malX | G | ABC transporter | ||
KDBJKIBH_00773 | 2.8e-126 | malR | K | Transcriptional regulator | ||
KDBJKIBH_00774 | 1.9e-40 | malR | K | Transcriptional regulator | ||
KDBJKIBH_00775 | 3.4e-304 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
KDBJKIBH_00776 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
KDBJKIBH_00778 | 1.5e-55 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
KDBJKIBH_00779 | 4.1e-81 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
KDBJKIBH_00780 | 1e-20 | 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) | |
KDBJKIBH_00781 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KDBJKIBH_00782 | 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 | |
KDBJKIBH_00783 | 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 | |
KDBJKIBH_00784 | 1.7e-40 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KDBJKIBH_00785 | 6.8e-20 | clpE | O | Belongs to the ClpA ClpB family | ||
KDBJKIBH_00786 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
KDBJKIBH_00787 | 1.8e-86 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
KDBJKIBH_00788 | 7.4e-49 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
KDBJKIBH_00789 | 6.9e-50 | yvaA | 1.1.1.371 | S | inositol 2-dehydrogenase activity | |
KDBJKIBH_00790 | 7e-26 | 2.7.7.15 | S | inositol 2-dehydrogenase activity | ||
KDBJKIBH_00791 | 4.6e-08 | S | oxidoreductase | |||
KDBJKIBH_00792 | 4.9e-232 | murN | 2.3.2.10, 2.3.2.16 | V | FemAB family | |
KDBJKIBH_00793 | 9.4e-71 | M | Pfam SNARE associated Golgi protein | |||
KDBJKIBH_00794 | 1.9e-99 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
KDBJKIBH_00797 | 1.2e-143 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
KDBJKIBH_00798 | 6e-33 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
KDBJKIBH_00801 | 1.9e-144 | pyrP | F | uracil Permease | ||
KDBJKIBH_00802 | 2.4e-54 | pyrP | F | uracil Permease | ||
KDBJKIBH_00803 | 1e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
KDBJKIBH_00804 | 5.5e-211 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
KDBJKIBH_00805 | 0.0 | carB | 6.3.5.5 | F | carbamoyl-phosphate synthetase ammonia chain | |
KDBJKIBH_00806 | 1.1e-133 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
KDBJKIBH_00807 | 3.6e-17 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
KDBJKIBH_00808 | 2e-36 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
KDBJKIBH_00809 | 8.4e-38 | V | permease protein | |||
KDBJKIBH_00810 | 2e-07 | V | efflux transmembrane transporter activity | |||
KDBJKIBH_00811 | 6.1e-30 | V | efflux transmembrane transporter activity | |||
KDBJKIBH_00812 | 3.1e-25 | V | permease protein | |||
KDBJKIBH_00814 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
KDBJKIBH_00815 | 2.6e-219 | ywbD | 2.1.1.191 | J | Methyltransferase | |
KDBJKIBH_00816 | 8.6e-122 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
KDBJKIBH_00817 | 8.2e-162 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
KDBJKIBH_00818 | 1e-201 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
KDBJKIBH_00819 | 2.1e-12 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
KDBJKIBH_00820 | 1.4e-189 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
KDBJKIBH_00821 | 3.8e-204 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
KDBJKIBH_00822 | 3.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
KDBJKIBH_00823 | 6.1e-97 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
KDBJKIBH_00824 | 1.2e-65 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
KDBJKIBH_00825 | 1.5e-203 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
KDBJKIBH_00826 | 5.4e-41 | 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 | ||
KDBJKIBH_00827 | 2.2e-174 | 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 | ||
KDBJKIBH_00828 | 1e-22 | bglC | K | Transcriptional regulator | ||
KDBJKIBH_00829 | 6.8e-60 | yfiF3 | K | sequence-specific DNA binding | ||
KDBJKIBH_00830 | 6.2e-39 | 3.1.3.6, 3.1.4.16 | F | nucleotide catabolic process | ||
KDBJKIBH_00831 | 1.6e-230 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_00833 | 9.2e-22 | yecS | P | amino acid transport | ||
KDBJKIBH_00834 | 2.5e-26 | yecS | P | ABC transporter (Permease | ||
KDBJKIBH_00835 | 7.9e-12 | artJ_1 | ET | Belongs to the bacterial solute-binding protein 3 family | ||
KDBJKIBH_00836 | 4.1e-99 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
KDBJKIBH_00837 | 3.4e-104 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
KDBJKIBH_00838 | 3.2e-74 | L | Transposase | |||
KDBJKIBH_00839 | 7.5e-103 | 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 | |
KDBJKIBH_00840 | 2.9e-125 | dnaD | ||||
KDBJKIBH_00841 | 1.3e-181 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
KDBJKIBH_00842 | 2e-94 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
KDBJKIBH_00843 | 0.0 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
KDBJKIBH_00844 | 1.5e-138 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KDBJKIBH_00845 | 2e-174 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
KDBJKIBH_00846 | 1.4e-90 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
KDBJKIBH_00847 | 6.1e-11 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
KDBJKIBH_00848 | 1.4e-44 | comFC | S | Competence protein | ||
KDBJKIBH_00849 | 5.9e-57 | comFC | S | Competence protein | ||
KDBJKIBH_00850 | 5.6e-128 | comFA | L | Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
KDBJKIBH_00851 | 1.4e-54 | comFA | L | Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
KDBJKIBH_00852 | 2.4e-110 | yvyE | 3.4.13.9 | S | YigZ family | |
KDBJKIBH_00853 | 2.8e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
KDBJKIBH_00854 | 7.7e-13 | acuB | S | IMP dehydrogenase activity | ||
KDBJKIBH_00855 | 2.5e-63 | acuB | S | CBS domain | ||
KDBJKIBH_00856 | 2.1e-123 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
KDBJKIBH_00857 | 8.2e-137 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
KDBJKIBH_00858 | 2.9e-70 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
KDBJKIBH_00859 | 9.7e-62 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
KDBJKIBH_00860 | 7.8e-27 | azlC | E | AzlC protein | ||
KDBJKIBH_00861 | 5.2e-133 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
KDBJKIBH_00862 | 3.3e-41 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
KDBJKIBH_00863 | 5.5e-41 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
KDBJKIBH_00864 | 5.6e-121 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
KDBJKIBH_00865 | 2.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
KDBJKIBH_00866 | 1.1e-186 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KDBJKIBH_00867 | 2.4e-113 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KDBJKIBH_00868 | 4.1e-41 | pscB | M | CHAP domain protein | ||
KDBJKIBH_00869 | 9.1e-53 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KDBJKIBH_00870 | 1.8e-153 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KDBJKIBH_00871 | 2.6e-25 | glnR | K | Transcriptional regulator | ||
KDBJKIBH_00872 | 2.3e-27 | glnR | K | Transcriptional regulator | ||
KDBJKIBH_00873 | 1.8e-87 | S | Fusaric acid resistance protein-like | |||
KDBJKIBH_00874 | 2.5e-12 | |||||
KDBJKIBH_00875 | 1.1e-30 | |||||
KDBJKIBH_00876 | 3.4e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
KDBJKIBH_00877 | 2.7e-41 | L | Transposase | |||
KDBJKIBH_00878 | 1.1e-43 | L | transposase activity | |||
KDBJKIBH_00879 | 5.7e-23 | L | Transposase | |||
KDBJKIBH_00880 | 3.5e-55 | L | transposition | |||
KDBJKIBH_00881 | 2.5e-17 | L | transposition | |||
KDBJKIBH_00882 | 1.1e-16 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
KDBJKIBH_00883 | 9.8e-147 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
KDBJKIBH_00884 | 4.7e-31 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
KDBJKIBH_00885 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
KDBJKIBH_00886 | 4.7e-73 | copY | K | Copper transport repressor, CopY TcrY family | ||
KDBJKIBH_00887 | 9.1e-104 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
KDBJKIBH_00888 | 5.2e-176 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
KDBJKIBH_00889 | 3e-44 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
KDBJKIBH_00890 | 1.2e-100 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
KDBJKIBH_00891 | 6.3e-46 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
KDBJKIBH_00892 | 3.9e-45 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
KDBJKIBH_00893 | 3.6e-177 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
KDBJKIBH_00894 | 2.2e-69 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
KDBJKIBH_00895 | 3.9e-122 | L | Transposase | |||
KDBJKIBH_00896 | 2e-88 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
KDBJKIBH_00897 | 1.2e-25 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
KDBJKIBH_00898 | 2.1e-35 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
KDBJKIBH_00899 | 6.2e-12 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
KDBJKIBH_00900 | 7.3e-70 | 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 | ||
KDBJKIBH_00901 | 2.1e-18 | 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 | ||
KDBJKIBH_00902 | 1.5e-36 | 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 | ||
KDBJKIBH_00903 | 1.1e-80 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
KDBJKIBH_00904 | 4.7e-20 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
KDBJKIBH_00905 | 2.8e-76 | XK27_09620 | S | reductase | ||
KDBJKIBH_00906 | 8.4e-60 | XK27_09615 | C | reductase | ||
KDBJKIBH_00907 | 2.7e-137 | XK27_09615 | C | reductase | ||
KDBJKIBH_00908 | 1.1e-07 | fnt | P | Formate nitrite transporter | ||
KDBJKIBH_00909 | 5.6e-92 | fnt | P | Formate nitrite transporter | ||
KDBJKIBH_00910 | 1.1e-48 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
KDBJKIBH_00911 | 1.8e-122 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
KDBJKIBH_00912 | 3.6e-39 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
KDBJKIBH_00913 | 4.2e-31 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KDBJKIBH_00914 | 4.5e-120 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KDBJKIBH_00915 | 3.6e-94 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
KDBJKIBH_00917 | 2.1e-100 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
KDBJKIBH_00918 | 4.5e-64 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
KDBJKIBH_00919 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
KDBJKIBH_00920 | 8.6e-66 | cah | 4.2.1.1 | P | carbonic anhydrase | |
KDBJKIBH_00921 | 1.8e-22 | cah | 4.2.1.1 | P | carbonate dehydratase activity | |
KDBJKIBH_00922 | 1.3e-84 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
KDBJKIBH_00923 | 8.8e-50 | hsdS_1 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
KDBJKIBH_00924 | 1.4e-30 | D | nuclear chromosome segregation | |||
KDBJKIBH_00925 | 2.7e-76 | L | DNA integration | |||
KDBJKIBH_00926 | 8.2e-88 | XK27_05540 | S | Gram-negative-bacterium-type cell wall biogenesis | ||
KDBJKIBH_00928 | 9.9e-239 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
KDBJKIBH_00929 | 2e-157 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
KDBJKIBH_00931 | 2.4e-75 | XK27_03180 | T | universal stress protein | ||
KDBJKIBH_00932 | 2.9e-113 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
KDBJKIBH_00933 | 6.3e-116 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
KDBJKIBH_00934 | 7e-14 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
KDBJKIBH_00935 | 2e-83 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
KDBJKIBH_00936 | 6.8e-101 | pncA | Q | isochorismatase | ||
KDBJKIBH_00937 | 2.3e-27 | endA | F | DNA RNA non-specific endonuclease | ||
KDBJKIBH_00938 | 2.6e-225 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KDBJKIBH_00939 | 2.6e-09 | S | Protein of unknown function (DUF1146) | |||
KDBJKIBH_00940 | 6e-196 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KDBJKIBH_00941 | 6e-27 | G | Domain of unknown function (DUF4832) | |||
KDBJKIBH_00942 | 5.4e-173 | 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 | |
KDBJKIBH_00943 | 1.6e-174 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
KDBJKIBH_00944 | 7e-130 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
KDBJKIBH_00945 | 1.4e-69 | 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 | ||
KDBJKIBH_00946 | 4.9e-297 | dnaK | O | Heat shock 70 kDa protein | ||
KDBJKIBH_00947 | 4.2e-190 | 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 | ||
KDBJKIBH_00948 | 7.7e-140 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
KDBJKIBH_00949 | 1.9e-110 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
KDBJKIBH_00950 | 9.2e-54 | hmpT | S | membrane | ||
KDBJKIBH_00951 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
KDBJKIBH_00952 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KDBJKIBH_00953 | 2.7e-85 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KDBJKIBH_00954 | 4.4e-55 | S | TM2 domain | |||
KDBJKIBH_00955 | 3e-42 | |||||
KDBJKIBH_00958 | 7e-33 | L | Integrase core domain protein | |||
KDBJKIBH_00959 | 8.7e-51 | L | transposition | |||
KDBJKIBH_00960 | 1.2e-09 | L | Transposase | |||
KDBJKIBH_00961 | 4.7e-24 | L | transposase activity | |||
KDBJKIBH_00962 | 4.1e-16 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KDBJKIBH_00963 | 2e-167 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KDBJKIBH_00964 | 1.3e-21 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
KDBJKIBH_00965 | 1.6e-81 | vraS | 2.7.13.3 | T | Histidine kinase | |
KDBJKIBH_00966 | 4.1e-18 | yvqF | KT | membrane | ||
KDBJKIBH_00967 | 2.1e-92 | yvqF | KT | membrane | ||
KDBJKIBH_00968 | 4.1e-09 | kcsA | P | Ion transport protein | ||
KDBJKIBH_00969 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
KDBJKIBH_00970 | 2e-132 | stp | 3.1.3.16 | T | phosphatase | |
KDBJKIBH_00971 | 2.9e-246 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
KDBJKIBH_00972 | 7.8e-174 | 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 | |
KDBJKIBH_00973 | 2.1e-105 | 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 | ||
KDBJKIBH_00974 | 2.7e-117 | 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 | ||
KDBJKIBH_00975 | 3.5e-180 | 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 | ||
KDBJKIBH_00976 | 4e-44 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
KDBJKIBH_00977 | 4.3e-32 | purM | 6.3.3.1, 6.3.4.13 | F | AIR synthase related protein, N-terminal domain | |
KDBJKIBH_00978 | 7.1e-20 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
KDBJKIBH_00979 | 1.3e-276 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
KDBJKIBH_00980 | 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 | |
KDBJKIBH_00981 | 8e-49 | 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 | |
KDBJKIBH_00982 | 7.6e-79 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
KDBJKIBH_00983 | 6.1e-37 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
KDBJKIBH_00984 | 2e-13 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
KDBJKIBH_00985 | 5e-25 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
KDBJKIBH_00986 | 9.2e-51 | dam | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
KDBJKIBH_00987 | 2.9e-17 | K | Cro/C1-type HTH DNA-binding domain | |||
KDBJKIBH_00988 | 1.7e-23 | |||||
KDBJKIBH_00989 | 1.4e-43 | |||||
KDBJKIBH_00990 | 7.2e-14 | |||||
KDBJKIBH_00991 | 1.3e-254 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KDBJKIBH_00992 | 5e-96 | mip | S | hydroperoxide reductase activity | ||
KDBJKIBH_00993 | 3.6e-191 | I | acyl-CoA dehydrogenase | |||
KDBJKIBH_00994 | 1e-149 | ydiA | P | C4-dicarboxylate transporter malic acid transport | ||
KDBJKIBH_00995 | 4.9e-244 | msrR | K | Transcriptional regulator | ||
KDBJKIBH_00996 | 9.7e-152 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
KDBJKIBH_00997 | 8.3e-27 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
KDBJKIBH_00998 | 4.8e-28 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
KDBJKIBH_00999 | 5.8e-34 | yvjA | S | membrane | ||
KDBJKIBH_01000 | 2.5e-59 | yvjA | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KDBJKIBH_01001 | 5.7e-305 | ybiT | S | abc transporter atp-binding protein | ||
KDBJKIBH_01002 | 0.0 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
KDBJKIBH_01006 | 8.1e-58 | yoaK | S | Psort location CytoplasmicMembrane, score | ||
KDBJKIBH_01007 | 8.9e-37 | yoaK | S | Psort location CytoplasmicMembrane, score | ||
KDBJKIBH_01008 | 1.7e-39 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
KDBJKIBH_01009 | 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 | |
KDBJKIBH_01010 | 4.6e-24 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
KDBJKIBH_01011 | 4.4e-172 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
KDBJKIBH_01012 | 1.7e-103 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
KDBJKIBH_01013 | 3.3e-138 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
KDBJKIBH_01014 | 1.8e-22 | dnaB | L | Replication initiation and membrane attachment | ||
KDBJKIBH_01015 | 1.5e-11 | dnaB | L | Replication initiation and membrane attachment | ||
KDBJKIBH_01016 | 4.3e-59 | dnaB | L | Replication initiation and membrane attachment | ||
KDBJKIBH_01017 | 4e-167 | dnaI | L | Primosomal protein DnaI | ||
KDBJKIBH_01018 | 7.4e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
KDBJKIBH_01019 | 3.5e-283 | P | ABC transporter transmembrane region | |||
KDBJKIBH_01021 | 3e-162 | 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 | ||
KDBJKIBH_01022 | 2.6e-18 | 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 | ||
KDBJKIBH_01023 | 9.9e-292 | 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 | ||
KDBJKIBH_01024 | 4.6e-88 | 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 | ||
KDBJKIBH_01025 | 1e-59 | 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 | ||
KDBJKIBH_01026 | 3.1e-53 | 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 | ||
KDBJKIBH_01027 | 7.7e-186 | S | CRISPR-associated protein Csn2 subfamily St | |||
KDBJKIBH_01028 | 1.2e-146 | ycgQ | S | TIGR03943 family | ||
KDBJKIBH_01029 | 2.3e-79 | XK27_03015 | S | permease | ||
KDBJKIBH_01030 | 8e-269 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
KDBJKIBH_01031 | 1.1e-96 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
KDBJKIBH_01032 | 4.7e-202 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
KDBJKIBH_01033 | 2.5e-49 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
KDBJKIBH_01034 | 3.2e-144 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
KDBJKIBH_01036 | 4e-09 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | G | Belongs to the glycosyl hydrolase 68 family |
KDBJKIBH_01037 | 4.4e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
KDBJKIBH_01039 | 1.2e-40 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
KDBJKIBH_01040 | 4.9e-34 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
KDBJKIBH_01041 | 8.3e-120 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_01042 | 1.3e-140 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_01043 | 1.4e-08 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_01044 | 3.1e-31 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
KDBJKIBH_01045 | 8.6e-148 | 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 | |
KDBJKIBH_01046 | 2.7e-157 | 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 | |
KDBJKIBH_01047 | 3.8e-34 | yugF | I | carboxylic ester hydrolase activity | ||
KDBJKIBH_01048 | 1.5e-07 | |||||
KDBJKIBH_01049 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
KDBJKIBH_01050 | 1.2e-77 | feoA | P | FeoA domain protein | ||
KDBJKIBH_01052 | 7.2e-41 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
KDBJKIBH_01053 | 6.7e-60 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
KDBJKIBH_01054 | 1.5e-83 | cas6 | S | Pfam:DUF2276 | ||
KDBJKIBH_01055 | 1.3e-179 | csm1 | S | CRISPR-associated protein Csm1 family | ||
KDBJKIBH_01056 | 2.1e-28 | csm1 | S | CRISPR-associated protein Csm1 family | ||
KDBJKIBH_01057 | 3.8e-88 | csm1 | S | CRISPR-associated protein Csm1 family | ||
KDBJKIBH_01058 | 5.6e-62 | csm2 | L | Pfam:DUF310 | ||
KDBJKIBH_01059 | 1.1e-116 | csm3 | L | RAMP superfamily | ||
KDBJKIBH_01060 | 2.8e-160 | csm4 | L | CRISPR-associated RAMP protein, Csm4 family | ||
KDBJKIBH_01061 | 3.7e-204 | csm5 | L | CRISPR-associated RAMP protein, Csm5 family | ||
KDBJKIBH_01062 | 4.4e-61 | csm6 | S | Psort location Cytoplasmic, score | ||
KDBJKIBH_01063 | 7e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
KDBJKIBH_01064 | 8.3e-111 | 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) | |
KDBJKIBH_01066 | 8.1e-48 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
KDBJKIBH_01067 | 1.6e-89 | lemA | S | LemA family | ||
KDBJKIBH_01068 | 3.5e-68 | htpX | O | Belongs to the peptidase M48B family | ||
KDBJKIBH_01069 | 9.3e-57 | htpX | O | Belongs to the peptidase M48B family | ||
KDBJKIBH_01070 | 3.6e-74 | S | Psort location CytoplasmicMembrane, score | |||
KDBJKIBH_01071 | 1.1e-55 | S | Domain of unknown function (DUF4430) | |||
KDBJKIBH_01072 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
KDBJKIBH_01073 | 2.5e-183 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
KDBJKIBH_01074 | 2.4e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
KDBJKIBH_01075 | 4.2e-112 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
KDBJKIBH_01076 | 6.2e-19 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
KDBJKIBH_01077 | 3.1e-161 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
KDBJKIBH_01078 | 6.5e-63 | dps | P | Belongs to the Dps family | ||
KDBJKIBH_01079 | 4.6e-29 | cbf | S | 3'-5' exoribonuclease yhaM | ||
KDBJKIBH_01080 | 1e-81 | cbf | S | 3'-5' exoribonuclease yhaM | ||
KDBJKIBH_01081 | 1.5e-172 | rmuC | S | RmuC domain protein | ||
KDBJKIBH_01082 | 2.4e-118 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
KDBJKIBH_01083 | 3e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
KDBJKIBH_01084 | 2.2e-162 | rsgA | 3.1.3.100 | G | 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 | |
KDBJKIBH_01086 | 2.6e-77 | 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 | |
KDBJKIBH_01087 | 2.5e-55 | 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 | |
KDBJKIBH_01088 | 1.1e-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 | |
KDBJKIBH_01089 | 7.8e-274 | 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) | |
KDBJKIBH_01090 | 1.8e-270 | 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) | |
KDBJKIBH_01091 | 1.4e-47 | 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) | |
KDBJKIBH_01092 | 4.4e-25 | 2.4.1.52 | GT4 | M | transferase activity, transferring glycosyl groups | |
KDBJKIBH_01093 | 7.4e-32 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
KDBJKIBH_01094 | 1.9e-211 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KDBJKIBH_01095 | 1.4e-34 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KDBJKIBH_01096 | 7.9e-96 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
KDBJKIBH_01097 | 2.1e-73 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
KDBJKIBH_01098 | 1.5e-192 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
KDBJKIBH_01100 | 1.6e-44 | V | 'abc transporter, ATP-binding protein | |||
KDBJKIBH_01101 | 3.4e-56 | V | 'abc transporter, ATP-binding protein | |||
KDBJKIBH_01104 | 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 | ||
KDBJKIBH_01106 | 2.3e-103 | 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 | ||
KDBJKIBH_01107 | 6.5e-145 | yaaA | S | Belongs to the UPF0246 family | ||
KDBJKIBH_01108 | 2.8e-116 | 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 | |
KDBJKIBH_01109 | 3.4e-91 | XK27_10930 | K | acetyltransferase | ||
KDBJKIBH_01110 | 7.5e-14 | |||||
KDBJKIBH_01111 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
KDBJKIBH_01112 | 1.4e-237 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
KDBJKIBH_01113 | 4.7e-24 | yrzB | S | Belongs to the UPF0473 family | ||
KDBJKIBH_01114 | 5.5e-69 | F | NUDIX domain | |||
KDBJKIBH_01115 | 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 | ||
KDBJKIBH_01116 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
KDBJKIBH_01117 | 2e-69 | rplI | J | binds to the 23S rRNA | ||
KDBJKIBH_01118 | 1.5e-107 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
KDBJKIBH_01119 | 1.7e-77 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
KDBJKIBH_01120 | 1.1e-169 | manN | G | PTS system mannose fructose sorbose family IID component | ||
KDBJKIBH_01121 | 6.5e-63 | manO | S | protein conserved in bacteria | ||
KDBJKIBH_01122 | 1.3e-232 | 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) | |
KDBJKIBH_01123 | 4.8e-91 | S | Protein of unknown function DUF262 | |||
KDBJKIBH_01124 | 7.8e-74 | S | Protein of unknown function DUF262 | |||
KDBJKIBH_01126 | 1.2e-13 | L | Transposase | |||
KDBJKIBH_01131 | 2.6e-10 | |||||
KDBJKIBH_01134 | 1.9e-07 | |||||
KDBJKIBH_01139 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KDBJKIBH_01140 | 2e-238 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KDBJKIBH_01141 | 5.1e-69 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KDBJKIBH_01142 | 5.3e-148 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
KDBJKIBH_01143 | 2.1e-91 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
KDBJKIBH_01144 | 1.1e-130 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
KDBJKIBH_01145 | 4.4e-242 | P | COG0168 Trk-type K transport systems, membrane components | |||
KDBJKIBH_01146 | 1.4e-121 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
KDBJKIBH_01147 | 2e-10 | ulaG | S | L-ascorbate 6-phosphate lactonase | ||
KDBJKIBH_01148 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
KDBJKIBH_01149 | 8.4e-65 | cbiQ | P | cobalt transport | ||
KDBJKIBH_01151 | 5.6e-223 | uup | S | abc transporter atp-binding protein | ||
KDBJKIBH_01152 | 5.1e-114 | uup | S | abc transporter atp-binding protein | ||
KDBJKIBH_01153 | 2.1e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
KDBJKIBH_01154 | 1.6e-178 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
KDBJKIBH_01155 | 8.1e-20 | 6.3.2.2, 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | ||
KDBJKIBH_01156 | 9.5e-71 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
KDBJKIBH_01157 | 1.3e-140 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
KDBJKIBH_01158 | 2.4e-56 | 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) | |
KDBJKIBH_01159 | 2e-180 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KDBJKIBH_01160 | 9e-110 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KDBJKIBH_01161 | 1.7e-184 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KDBJKIBH_01163 | 1.4e-71 | L | Transposase (IS116 IS110 IS902 family) | |||
KDBJKIBH_01164 | 1.6e-61 | L | Transposase (IS116 IS110 IS902 family) | |||
KDBJKIBH_01165 | 7e-29 | ypuA | S | secreted protein | ||
KDBJKIBH_01166 | 8.9e-64 | ypuA | S | secreted protein | ||
KDBJKIBH_01167 | 3.4e-112 | 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 | ||
KDBJKIBH_01168 | 2.3e-60 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
KDBJKIBH_01169 | 1.7e-26 | sepF | D | cell septum assembly | ||
KDBJKIBH_01170 | 4.2e-16 | 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 | ||
KDBJKIBH_01171 | 7.2e-144 | ylmH | T | S4 RNA-binding domain | ||
KDBJKIBH_01172 | 7.9e-136 | divIVA | D | Cell division protein DivIVA | ||
KDBJKIBH_01173 | 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) | |
KDBJKIBH_01174 | 1.8e-72 | ycbB | S | Glycosyl transferase family 2 | ||
KDBJKIBH_01175 | 1.9e-115 | 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 | |
KDBJKIBH_01176 | 2.2e-19 | 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 | |
KDBJKIBH_01177 | 3.9e-243 | |||||
KDBJKIBH_01178 | 1.6e-171 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
KDBJKIBH_01179 | 2.8e-169 | M | Psort location CytoplasmicMembrane, score | |||
KDBJKIBH_01180 | 4.2e-15 | M | Psort location CytoplasmicMembrane, score | |||
KDBJKIBH_01181 | 2.2e-28 | V | ATPase activity | |||
KDBJKIBH_01182 | 7.3e-172 | oppF | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_01183 | 4.9e-204 | oppD | P | Belongs to the ABC transporter superfamily | ||
KDBJKIBH_01184 | 4.9e-168 | amiD | P | ABC transporter (Permease | ||
KDBJKIBH_01185 | 7.1e-278 | amiC | P | ABC transporter (Permease | ||
KDBJKIBH_01186 | 2.7e-162 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
KDBJKIBH_01187 | 4.8e-120 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
KDBJKIBH_01188 | 5.5e-50 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
KDBJKIBH_01189 | 9.3e-272 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
KDBJKIBH_01190 | 2.5e-77 | ureE | O | enzyme active site formation | ||
KDBJKIBH_01191 | 5.3e-130 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
KDBJKIBH_01193 | 6.4e-84 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
KDBJKIBH_01194 | 1.2e-160 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
KDBJKIBH_01195 | 9.4e-41 | cbiM | P | PDGLE domain | ||
KDBJKIBH_01196 | 5.5e-107 | cbiM | P | PDGLE domain | ||
KDBJKIBH_01197 | 1e-87 | P | cobalt transport protein | |||
KDBJKIBH_01199 | 9.8e-112 | 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 | ||
KDBJKIBH_01200 | 9.7e-121 | 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 | ||
KDBJKIBH_01201 | 1.7e-175 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
KDBJKIBH_01202 | 1.3e-201 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
KDBJKIBH_01203 | 7.3e-83 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KDBJKIBH_01204 | 4.5e-104 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
KDBJKIBH_01205 | 1.8e-15 | metE | 2.1.1.14 | E | Methionine synthase | |
KDBJKIBH_01206 | 1.8e-136 | metE | 2.1.1.14 | E | Methionine synthase | |
KDBJKIBH_01207 | 1.2e-241 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
KDBJKIBH_01209 | 1.2e-18 | 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) | |
KDBJKIBH_01210 | 1.2e-296 | 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) | |
KDBJKIBH_01211 | 4.5e-104 | XK27_01785 | S | cog cog1284 | ||
KDBJKIBH_01212 | 3.2e-28 | XK27_01785 | S | cog cog1284 | ||
KDBJKIBH_01213 | 8.6e-89 | 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) | |
KDBJKIBH_01214 | 1.7e-26 | 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) | |
KDBJKIBH_01215 | 7.9e-39 | ptsH | G | phosphocarrier protein Hpr | ||
KDBJKIBH_01216 | 3.8e-35 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
KDBJKIBH_01217 | 5.6e-107 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
KDBJKIBH_01218 | 2.6e-62 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
KDBJKIBH_01219 | 1.5e-211 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
KDBJKIBH_01220 | 5.7e-233 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
KDBJKIBH_01221 | 2.8e-89 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
KDBJKIBH_01222 | 2.4e-104 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
KDBJKIBH_01223 | 4.6e-91 | yocD | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
KDBJKIBH_01224 | 1.8e-75 | yocD | 3.4.17.13 | V | carboxypeptidase activity | |
KDBJKIBH_01226 | 3.2e-40 | L | transposition | |||
KDBJKIBH_01227 | 1e-87 | L | Integrase core domain protein | |||
KDBJKIBH_01228 | 4.7e-48 | S | reductase | |||
KDBJKIBH_01229 | 4.1e-30 | S | reductase | |||
KDBJKIBH_01230 | 5.7e-55 | badR | K | DNA-binding transcription factor activity | ||
KDBJKIBH_01231 | 5.5e-36 | XK27_02060 | S | Transglycosylase associated protein | ||
KDBJKIBH_01232 | 2.5e-53 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
KDBJKIBH_01233 | 4.3e-46 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
KDBJKIBH_01234 | 9.5e-55 | yabA | L | Involved in initiation control of chromosome replication | ||
KDBJKIBH_01235 | 9.3e-102 | yaaT | S | stage 0 sporulation protein | ||
KDBJKIBH_01236 | 1.9e-161 | holB | 2.7.7.7 | L | dna polymerase iii | |
KDBJKIBH_01237 | 1.7e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KDBJKIBH_01238 | 1.4e-136 | 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) | |
KDBJKIBH_01239 | 7e-223 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
KDBJKIBH_01240 | 1.6e-196 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
KDBJKIBH_01241 | 1.3e-19 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
KDBJKIBH_01242 | 2e-50 | sthIM | 2.1.1.72 | L | Adenine specific DNA methylase Mod | |
KDBJKIBH_01244 | 1.9e-110 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
KDBJKIBH_01245 | 1.3e-39 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
KDBJKIBH_01246 | 1.5e-08 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
KDBJKIBH_01247 | 2.1e-07 | |||||
KDBJKIBH_01248 | 1.4e-23 | |||||
KDBJKIBH_01249 | 4.8e-140 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
KDBJKIBH_01250 | 7.6e-310 | 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 | |
KDBJKIBH_01251 | 2.9e-84 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
KDBJKIBH_01252 | 3.1e-80 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
KDBJKIBH_01253 | 9.1e-178 | prmA | J | Ribosomal protein L11 methyltransferase | ||
KDBJKIBH_01254 | 4.4e-135 | 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 | |
KDBJKIBH_01255 | 3.3e-82 | K | DNA-binding helix-turn-helix protein | |||
KDBJKIBH_01256 | 1.7e-102 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
KDBJKIBH_01257 | 1.2e-135 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KDBJKIBH_01258 | 6.1e-132 | GK | ROK family | |||
KDBJKIBH_01259 | 2.1e-126 | dprA | LU | DNA protecting protein DprA | ||
KDBJKIBH_01260 | 3.1e-17 | 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 | |
KDBJKIBH_01261 | 9.9e-138 | 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) | |
KDBJKIBH_01262 | 3.2e-28 | 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) | |
KDBJKIBH_01263 | 8e-25 | |||||
KDBJKIBH_01264 | 3.8e-218 | araT | 2.6.1.1 | E | Aminotransferase | |
KDBJKIBH_01265 | 7e-144 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
KDBJKIBH_01266 | 2.9e-140 | 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 | |
KDBJKIBH_01267 | 5.7e-32 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
KDBJKIBH_01268 | 1.2e-114 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
KDBJKIBH_01269 | 1.5e-28 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
KDBJKIBH_01270 | 4.4e-183 | ccpA | K | Catabolite control protein A | ||
KDBJKIBH_01271 | 2.8e-28 | yyaQ | S | YjbR | ||
KDBJKIBH_01272 | 3.4e-143 | yyaQ | S | YjbR | ||
KDBJKIBH_01273 | 1.2e-39 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KDBJKIBH_01274 | 6.7e-159 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KDBJKIBH_01275 | 2.2e-49 | yueI | S | Protein of unknown function (DUF1694) | ||
KDBJKIBH_01276 | 1.4e-13 | yueI | S | Protein of unknown function (DUF1694) | ||
KDBJKIBH_01277 | 2.5e-35 | 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 | |
KDBJKIBH_01278 | 9.4e-10 | M | transferase activity, transferring glycosyl groups | |||
KDBJKIBH_01279 | 1.5e-33 | L | transposase activity | |||
KDBJKIBH_01280 | 3e-156 | L | COG2801 Transposase and inactivated derivatives | |||
KDBJKIBH_01281 | 1.3e-122 | tnp | L | DDE domain | ||
KDBJKIBH_01282 | 9e-40 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
KDBJKIBH_01283 | 4.1e-73 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
KDBJKIBH_01284 | 4.5e-41 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
KDBJKIBH_01285 | 7.2e-08 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
KDBJKIBH_01286 | 4.1e-57 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
KDBJKIBH_01287 | 5.7e-27 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
KDBJKIBH_01288 | 2.3e-75 | 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 | ||
KDBJKIBH_01289 | 7e-190 | 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 | |
KDBJKIBH_01290 | 7.7e-39 | ctpE | P | E1-E2 ATPase | ||
KDBJKIBH_01291 | 1.6e-133 | ctpE | P | E1-E2 ATPase | ||
KDBJKIBH_01293 | 4.1e-96 | ctpE | P | E1-E2 ATPase | ||
KDBJKIBH_01294 | 6.1e-27 | |||||
KDBJKIBH_01295 | 1.9e-23 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
KDBJKIBH_01296 | 1.9e-46 | L | transposase activity | |||
KDBJKIBH_01297 | 1.4e-36 | L | transposition | |||
KDBJKIBH_01298 | 4.9e-42 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KDBJKIBH_01299 | 5.4e-49 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KDBJKIBH_01300 | 1.5e-234 | vicK | 2.7.13.3 | T | Histidine kinase | |
KDBJKIBH_01301 | 2.2e-156 | vicX | 3.1.26.11 | S | Metal-dependent hydrolases of the beta-lactamase superfamily I | |
KDBJKIBH_01302 | 1.5e-34 | F | Protein of unknown function (DUF454) | |||
KDBJKIBH_01303 | 5.3e-231 | murM | 2.3.2.10, 2.3.2.16 | V | protein involved in methicillin resistance | |
KDBJKIBH_01304 | 7.7e-100 | yidA | S | hydrolases of the HAD superfamily | ||
KDBJKIBH_01305 | 9.5e-107 | mprF | 2.3.2.3 | J | 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 | |
KDBJKIBH_01306 | 1e-142 | mprF | 2.3.2.3 | J | 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 | |
KDBJKIBH_01307 | 8.2e-44 | mprF | 2.3.2.3 | J | 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 | |
KDBJKIBH_01308 | 3.3e-149 | cobQ | S | glutamine amidotransferase | ||
KDBJKIBH_01309 | 1.6e-257 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
KDBJKIBH_01310 | 1.9e-107 | S | Domain of unknown function (DUF1803) | |||
KDBJKIBH_01311 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
KDBJKIBH_01312 | 7.3e-133 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
KDBJKIBH_01313 | 1.4e-259 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KDBJKIBH_01314 | 6e-117 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
KDBJKIBH_01315 | 2e-67 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
KDBJKIBH_01316 | 2.1e-67 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KDBJKIBH_01317 | 1.8e-29 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KDBJKIBH_01318 | 1.4e-136 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
KDBJKIBH_01319 | 1.1e-155 | cjaA | ET | ABC transporter substrate-binding protein | ||
KDBJKIBH_01321 | 1.5e-258 | 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 | |
KDBJKIBH_01322 | 9.9e-07 | U | response to pH | |||
KDBJKIBH_01323 | 1.1e-67 | yfmR | S | abc transporter atp-binding protein | ||
KDBJKIBH_01324 | 3.7e-249 | yfmR | S | abc transporter atp-binding protein | ||
KDBJKIBH_01325 | 1.5e-225 | 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 | |
KDBJKIBH_01326 | 5.1e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
KDBJKIBH_01327 | 1.6e-106 | XK27_08360 | T | EDD domain protein, DegV family | ||
KDBJKIBH_01328 | 2.9e-31 | XK27_08360 | S | lipid binding | ||
KDBJKIBH_01329 | 1.9e-29 | ypmB | S | Protein conserved in bacteria | ||
KDBJKIBH_01330 | 6.5e-218 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
KDBJKIBH_01331 | 2e-241 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
KDBJKIBH_01333 | 8.1e-08 | |||||
KDBJKIBH_01334 | 2.1e-22 | L | Transposase | |||
KDBJKIBH_01335 | 6.1e-18 | L | Transposase | |||
KDBJKIBH_01336 | 2.6e-66 | sigH | K | DNA-templated transcription, initiation | ||
KDBJKIBH_01337 | 3.4e-148 | ykuT | M | mechanosensitive ion channel | ||
KDBJKIBH_01338 | 5.5e-90 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
KDBJKIBH_01339 | 1.3e-33 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
KDBJKIBH_01340 | 4.8e-11 | |||||
KDBJKIBH_01341 | 3.1e-68 | nudG | 3.6.1.55, 3.6.1.65 | L | Belongs to the Nudix hydrolase family | |
KDBJKIBH_01342 | 1.5e-100 | L | helicase | |||
KDBJKIBH_01343 | 1.7e-126 | L | helicase | |||
KDBJKIBH_01344 | 3.1e-231 | L | helicase | |||
KDBJKIBH_01345 | 6.8e-102 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
KDBJKIBH_01346 | 2.7e-101 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
KDBJKIBH_01347 | 4.1e-38 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
KDBJKIBH_01348 | 1.9e-132 | rr02 | KT | response regulator | ||
KDBJKIBH_01349 | 1.7e-44 | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | ||
KDBJKIBH_01350 | 1.6e-134 | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | ||
KDBJKIBH_01351 | 2.8e-168 | V | ABC transporter | |||
KDBJKIBH_01352 | 5.4e-122 | sagI | S | ABC-2 type transporter | ||
KDBJKIBH_01353 | 3.4e-126 | yceA | S | Belongs to the UPF0176 family | ||
KDBJKIBH_01354 | 8e-70 | 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 | |
KDBJKIBH_01355 | 4.4e-97 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
KDBJKIBH_01356 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
KDBJKIBH_01357 | 3.3e-98 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
KDBJKIBH_01358 | 5.2e-78 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
KDBJKIBH_01359 | 5.5e-24 | 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 | ||
KDBJKIBH_01360 | 1.7e-63 | licT | K | transcriptional antiterminator | ||
KDBJKIBH_01361 | 1.1e-43 | licT | K | transcriptional antiterminator | ||
KDBJKIBH_01362 | 8.3e-37 | 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 | |
KDBJKIBH_01363 | 1.7e-64 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
KDBJKIBH_01364 | 2.2e-165 | era | M | 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 | ||
KDBJKIBH_01365 | 3e-153 | 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 | |
KDBJKIBH_01366 | 3.8e-19 | D | nuclear chromosome segregation | |||
KDBJKIBH_01367 | 6.5e-95 | queF | 1.7.1.13 | S | Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily | |
KDBJKIBH_01368 | 9.3e-135 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
KDBJKIBH_01369 | 3.6e-82 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
KDBJKIBH_01370 | 4e-124 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
KDBJKIBH_01371 | 1.1e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
KDBJKIBH_01372 | 1.2e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
KDBJKIBH_01373 | 1.5e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
KDBJKIBH_01374 | 9.7e-32 | 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 | ||
KDBJKIBH_01375 | 2.3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
KDBJKIBH_01376 | 1.1e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
KDBJKIBH_01377 | 1.7e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
KDBJKIBH_01378 | 2.5e-23 | rpmD | J | ribosomal protein l30 | ||
KDBJKIBH_01379 | 4.4e-58 | rplO | J | binds to the 23S rRNA | ||
KDBJKIBH_01380 | 9.6e-147 | 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 | ||
KDBJKIBH_01381 | 2.8e-58 | 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 | ||
KDBJKIBH_01382 | 3.1e-38 | 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 | |
KDBJKIBH_01383 | 9.7e-40 | 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 | |
KDBJKIBH_01384 | 2e-16 | 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 | ||
KDBJKIBH_01385 | 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 | |
KDBJKIBH_01386 | 1.3e-85 | ccl | S | cog cog4708 | ||
KDBJKIBH_01387 | 7.4e-164 | rbn | E | Belongs to the UPF0761 family | ||
KDBJKIBH_01388 | 5e-159 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
KDBJKIBH_01389 | 8.8e-25 | ytoI | K | transcriptional regulator containing CBS domains | ||
KDBJKIBH_01390 | 2.5e-91 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
KDBJKIBH_01391 | 6.7e-88 | ribU | 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 | ||
KDBJKIBH_01392 | 1.1e-62 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
KDBJKIBH_01393 | 3.3e-161 | K | sequence-specific DNA binding | |||
KDBJKIBH_01394 | 9.4e-33 | V | protein secretion by the type I secretion system | |||
KDBJKIBH_01395 | 2.1e-78 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
KDBJKIBH_01396 | 2.6e-43 | V | protein secretion by the type I secretion system | |||
KDBJKIBH_01397 | 1.8e-27 | comA | V | protein secretion by the type I secretion system | ||
KDBJKIBH_01398 | 5.2e-22 | comA | V | protein secretion by the type I secretion system | ||
KDBJKIBH_01399 | 3.4e-68 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
KDBJKIBH_01400 | 9.8e-46 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
KDBJKIBH_01401 | 4e-22 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
KDBJKIBH_01402 | 8.1e-143 | yjcE | P | NhaP-type Na H and K H antiporters | ||
KDBJKIBH_01403 | 1.6e-181 | yjcE | P | NhaP-type Na H and K H antiporters | ||
KDBJKIBH_01405 | 2.4e-98 | ytqB | 2.1.1.176 | J | (SAM)-dependent | |
KDBJKIBH_01406 | 5.3e-101 | yhcC | S | radical SAM protein | ||
KDBJKIBH_01407 | 1.1e-19 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KDBJKIBH_01408 | 7e-56 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KDBJKIBH_01409 | 1.3e-229 | noxE | P | NADH oxidase | ||
KDBJKIBH_01410 | 2.5e-294 | yfmM | S | abc transporter atp-binding protein | ||
KDBJKIBH_01412 | 2e-56 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
KDBJKIBH_01413 | 1.6e-109 | S | CAAX amino terminal protease family protein | |||
KDBJKIBH_01415 | 7e-62 | V | CAAX protease self-immunity | |||
KDBJKIBH_01416 | 2.9e-09 | lanR | K | sequence-specific DNA binding | ||
KDBJKIBH_01417 | 3e-215 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KDBJKIBH_01418 | 2.1e-26 | ytxK | 2.1.1.72 | L | DNA methylase | |
KDBJKIBH_01419 | 1.4e-121 | ytxK | 2.1.1.72 | L | DNA methylase | |
KDBJKIBH_01420 | 6.2e-36 | comGF | U | Putative Competence protein ComGF | ||
KDBJKIBH_01421 | 5.4e-15 | NU | Type II secretory pathway pseudopilin | |||
KDBJKIBH_01422 | 4.4e-17 | cglD | NU | Competence protein | ||
KDBJKIBH_01423 | 2.4e-31 | cglD | NU | Competence protein | ||
KDBJKIBH_01424 | 8.5e-43 | comGC | U | Required for transformation and DNA binding | ||
KDBJKIBH_01425 | 6.9e-44 | cglB | NU | type II secretion system | ||
KDBJKIBH_01426 | 8.2e-94 | cglB | NU | type II secretion system | ||
KDBJKIBH_01427 | 4.6e-92 | XK27_08835 | S | ABC transporter substrate binding protein | ||
KDBJKIBH_01428 | 5.2e-148 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
KDBJKIBH_01429 | 1.2e-135 | XK27_08845 | S | abc transporter atp-binding protein | ||
KDBJKIBH_01430 | 4.6e-310 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KDBJKIBH_01431 | 6.6e-150 | estA | CE1 | S | Putative esterase | |
KDBJKIBH_01432 | 7e-64 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KDBJKIBH_01433 | 8.9e-170 | 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 | ||
KDBJKIBH_01434 | 4.9e-41 | pspC | KT | PspC domain | ||
KDBJKIBH_01435 | 4.9e-86 | ydcK | S | Belongs to the SprT family | ||
KDBJKIBH_01436 | 0.0 | yhgF | K | Transcriptional accessory protein | ||
KDBJKIBH_01437 | 2.2e-35 | yhgF | K | Transcriptional accessory protein | ||
KDBJKIBH_01438 | 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 | |
KDBJKIBH_01439 | 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 | |
KDBJKIBH_01440 | 2.1e-65 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KDBJKIBH_01441 | 1.5e-77 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
KDBJKIBH_01442 | 1.4e-167 | fhuR | K | transcriptional regulator (lysR family) | ||
KDBJKIBH_01448 | 1.8e-143 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
KDBJKIBH_01449 | 1.1e-32 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
KDBJKIBH_01450 | 1.5e-32 | salL | 2.5.1.63, 2.5.1.94 | F | Pfam S-adenosyl-l-methionine hydroxide adenosyltransferase | |
KDBJKIBH_01451 | 9.2e-77 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
KDBJKIBH_01452 | 8e-94 | S | UPF0397 protein | |||
KDBJKIBH_01453 | 0.0 | ykoD | P | abc transporter atp-binding protein | ||
KDBJKIBH_01454 | 2.7e-61 | KT | phosphorelay signal transduction system | |||
KDBJKIBH_01455 | 6.6e-15 | S | Protein of unknown function (DUF3021) | |||
KDBJKIBH_01456 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
KDBJKIBH_01457 | 1.9e-30 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
KDBJKIBH_01458 | 1.2e-27 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
KDBJKIBH_01459 | 2e-42 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
KDBJKIBH_01460 | 1.6e-160 | 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 | |
KDBJKIBH_01461 | 6.7e-139 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
KDBJKIBH_01462 | 4.7e-90 | 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) | |
KDBJKIBH_01463 | 3.3e-131 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
KDBJKIBH_01464 | 1.4e-127 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
KDBJKIBH_01465 | 2.7e-39 | pepF | E | oligoendopeptidase F | ||
KDBJKIBH_01466 | 1.8e-194 | pepF | E | oligoendopeptidase F | ||
KDBJKIBH_01467 | 5.3e-186 | coiA | 3.6.4.12 | S | Competence protein | |
KDBJKIBH_01468 | 6.6e-45 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KDBJKIBH_01469 | 3.6e-202 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KDBJKIBH_01470 | 7.5e-09 | |||||
KDBJKIBH_01471 | 1.6e-84 | L | Transposase | |||
KDBJKIBH_01472 | 1.1e-26 | |||||
KDBJKIBH_01473 | 5.8e-50 | bioY | S | biotin synthase | ||
KDBJKIBH_01474 | 2e-49 | S | CHY zinc finger | |||
KDBJKIBH_01475 | 3.4e-252 | yegQ | O | Peptidase U32 | ||
KDBJKIBH_01476 | 1.9e-112 | yegQ | O | Peptidase U32 | ||
KDBJKIBH_01477 | 4.4e-13 | yegQ | O | Peptidase U32 | ||
KDBJKIBH_01479 | 5.5e-69 | ytxH | S | General stress protein | ||
KDBJKIBH_01481 | 8.1e-12 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KDBJKIBH_01482 | 2.8e-67 | 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 | |
KDBJKIBH_01484 | 2.9e-90 | ebsA | S | Family of unknown function (DUF5322) | ||
KDBJKIBH_01485 | 5.3e-93 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KDBJKIBH_01486 | 3.6e-91 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KDBJKIBH_01487 | 7.9e-97 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KDBJKIBH_01488 | 2e-71 | G | COG0457 FOG TPR repeat | |||
KDBJKIBH_01489 | 2.2e-75 | pbuX | F | xanthine permease | ||
KDBJKIBH_01490 | 7.8e-77 | 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 | |
KDBJKIBH_01491 | 6e-123 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KDBJKIBH_01492 | 4.1e-129 | T | Histidine kinase | |||
KDBJKIBH_01493 | 4e-67 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
KDBJKIBH_01494 | 5.7e-71 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
KDBJKIBH_01495 | 2e-45 | rpmE2 | J | 50S ribosomal protein L31 | ||
KDBJKIBH_01496 | 1.5e-177 | 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 | |
KDBJKIBH_01497 | 3.9e-142 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
KDBJKIBH_01498 | 9.1e-18 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
KDBJKIBH_01499 | 1.1e-42 | gst | O | Glutathione S-transferase | ||
KDBJKIBH_01500 | 3.5e-80 | gst | O | Glutathione S-transferase | ||
KDBJKIBH_01501 | 1.7e-121 | 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 | |
KDBJKIBH_01502 | 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 | |
KDBJKIBH_01503 | 5.9e-54 | 2.3.1.128, 5.2.1.8 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
KDBJKIBH_01504 | 2e-45 | S | FMN binding | |||
KDBJKIBH_01505 | 9.4e-52 | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | |||
KDBJKIBH_01506 | 1.1e-53 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KDBJKIBH_01507 | 1.8e-11 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KDBJKIBH_01508 | 2.9e-87 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KDBJKIBH_01512 | 3e-47 | spiA | K | sequence-specific DNA binding | ||
KDBJKIBH_01513 | 3.1e-111 | blpT | ||||
KDBJKIBH_01514 | 9.6e-21 | L | Transposase | |||
KDBJKIBH_01515 | 1.2e-69 | comEC | S | Competence protein ComEC | ||
KDBJKIBH_01516 | 5.3e-57 | comEC | S | Competence protein ComEC | ||
KDBJKIBH_01517 | 6.2e-61 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
KDBJKIBH_01518 | 1.7e-24 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
KDBJKIBH_01519 | 8.8e-76 | L | integrase core domain | |||
KDBJKIBH_01520 | 1.1e-37 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
KDBJKIBH_01521 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KDBJKIBH_01522 | 5.9e-13 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KDBJKIBH_01523 | 3.3e-164 | dnaE | 2.7.7.7 | L | DNA polymerase | |
KDBJKIBH_01524 | 3.2e-127 | sua5 | 2.7.7.87 | J | Belongs to the SUA5 family | |
KDBJKIBH_01525 | 5.1e-14 | sua5 | 2.7.7.87 | J | Belongs to the SUA5 family | |
KDBJKIBH_01526 | 2.5e-39 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KDBJKIBH_01527 | 2.5e-19 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KDBJKIBH_01528 | 6.5e-25 | metI | P | ABC transporter (Permease | ||
KDBJKIBH_01529 | 5.6e-26 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KDBJKIBH_01530 | 2.1e-48 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KDBJKIBH_01531 | 7.5e-30 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KDBJKIBH_01532 | 5.3e-20 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase activity | |
KDBJKIBH_01533 | 3.9e-20 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase activity | |
KDBJKIBH_01534 | 1.1e-164 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
KDBJKIBH_01535 | 5.1e-30 | metQ | M | Belongs to the NlpA lipoprotein family | ||
KDBJKIBH_01536 | 8.3e-29 | metQ | M | Belongs to the NlpA lipoprotein family | ||
KDBJKIBH_01537 | 1.9e-60 | ET | amino acid transport | |||
KDBJKIBH_01538 | 6.9e-36 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
KDBJKIBH_01539 | 3.5e-106 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
KDBJKIBH_01540 | 7.6e-101 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
KDBJKIBH_01541 | 4e-175 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
KDBJKIBH_01542 | 3.2e-181 | norM | V | Multidrug efflux pump | ||
KDBJKIBH_01543 | 7.7e-79 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KDBJKIBH_01544 | 3e-147 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KDBJKIBH_01545 | 2e-146 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
KDBJKIBH_01546 | 2.9e-99 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
KDBJKIBH_01547 | 7.4e-286 | ydaO | E | amino acid | ||
KDBJKIBH_01548 | 4.3e-50 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
KDBJKIBH_01549 | 6e-25 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
KDBJKIBH_01550 | 1.7e-102 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
KDBJKIBH_01551 | 6.4e-97 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
KDBJKIBH_01552 | 1.8e-31 | yxkH | G | deacetylase | ||
KDBJKIBH_01553 | 2.1e-89 | yxkH | G | deacetylase | ||
KDBJKIBH_01554 | 2.7e-219 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
KDBJKIBH_01555 | 7e-123 | |||||
KDBJKIBH_01557 | 2.7e-26 | IQ | PFAM AMP-dependent synthetase and ligase | |||
KDBJKIBH_01558 | 1.6e-25 | MA20_06410 | E | LysE type translocator | ||
KDBJKIBH_01559 | 6.8e-50 | MA20_06410 | E | LysE type translocator | ||
KDBJKIBH_01560 | 1.4e-12 | |||||
KDBJKIBH_01561 | 7.4e-158 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
KDBJKIBH_01562 | 9.8e-77 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
KDBJKIBH_01563 | 2e-138 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
KDBJKIBH_01564 | 9.5e-31 | M1-755 | P | Hemerythrin HHE cation binding domain protein | ||
KDBJKIBH_01565 | 3.1e-110 | hsdS2 | 2.1.1.72 | V | Type I restriction modification DNA specificity domain | |
KDBJKIBH_01566 | 2.7e-73 | 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 | |
KDBJKIBH_01567 | 1.1e-24 | fruR | K | transcriptional | ||
KDBJKIBH_01568 | 1.8e-78 | fruR | K | transcriptional | ||
KDBJKIBH_01569 | 5.3e-20 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
KDBJKIBH_01570 | 1.5e-92 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
KDBJKIBH_01571 | 2.1e-52 | fruA | 2.7.1.202 | GT | PTS system, Lactose/Cellobiose specific IIB subunit | |
KDBJKIBH_01572 | 7.3e-12 | fruA | 2.7.1.202 | GT | PTS system, Lactose/Cellobiose specific IIB subunit | |
KDBJKIBH_01573 | 7.8e-22 | fruA | 2.7.1.202 | GT | PTS system, Lactose/Cellobiose specific IIB subunit | |
KDBJKIBH_01574 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
KDBJKIBH_01575 | 8e-100 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
KDBJKIBH_01576 | 7.6e-291 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
KDBJKIBH_01577 | 2.5e-11 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
KDBJKIBH_01578 | 1.2e-56 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
KDBJKIBH_01579 | 7.3e-155 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
KDBJKIBH_01580 | 4.9e-21 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
KDBJKIBH_01581 | 1.8e-167 | 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) | |
KDBJKIBH_01582 | 6.5e-128 | K | sequence-specific DNA binding | |||
KDBJKIBH_01583 | 3.5e-70 | KLT | serine threonine protein kinase | |||
KDBJKIBH_01584 | 3.3e-167 | S | hmm pf01594 | |||
KDBJKIBH_01585 | 2.9e-27 | bglH | 3.2.1.86 | GT1 | G | beta-glucosidase activity |
KDBJKIBH_01586 | 4.6e-36 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KDBJKIBH_01587 | 3.2e-42 | bglH | 3.2.1.86 | GT1 | G | beta-glucosidase activity |
KDBJKIBH_01588 | 1.1e-36 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
KDBJKIBH_01589 | 1.4e-38 | S | granule-associated protein | |||
KDBJKIBH_01590 | 4e-173 | S | unusual protein kinase | |||
KDBJKIBH_01591 | 1.1e-26 | yeeD | O | sulfur carrier activity | ||
KDBJKIBH_01592 | 4.4e-48 | ssb_2 | 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 | ||
KDBJKIBH_01593 | 7.8e-83 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
KDBJKIBH_01596 | 1.9e-07 | 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 | ||
KDBJKIBH_01597 | 1.3e-25 | 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 | ||
KDBJKIBH_01598 | 2e-115 | 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 | ||
KDBJKIBH_01599 | 1.2e-11 | |||||
KDBJKIBH_01600 | 1.2e-91 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
KDBJKIBH_01601 | 2.7e-125 | 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 | |
KDBJKIBH_01603 | 1.8e-195 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
KDBJKIBH_01604 | 9.3e-184 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
KDBJKIBH_01605 | 8.5e-39 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
KDBJKIBH_01606 | 1.8e-88 | fruA | 2.7.1.202 | G | phosphotransferase system | |
KDBJKIBH_01608 | 2e-55 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
KDBJKIBH_01609 | 1.5e-32 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
KDBJKIBH_01610 | 3.8e-84 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
KDBJKIBH_01611 | 1.3e-136 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
KDBJKIBH_01612 | 2.3e-84 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
KDBJKIBH_01613 | 1.1e-27 | XK27_02070 | S | nitroreductase | ||
KDBJKIBH_01614 | 1.7e-35 | XK27_02070 | S | nitroreductase | ||
KDBJKIBH_01615 | 8.2e-36 | 1.13.11.2 | S | glyoxalase | ||
KDBJKIBH_01617 | 3.8e-111 | E | Alpha/beta hydrolase of unknown function (DUF915) | |||
KDBJKIBH_01618 | 9.1e-37 | 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 | ||
KDBJKIBH_01619 | 8e-27 | S | Protein of unknown function (DUF3114) | |||
KDBJKIBH_01620 | 2.4e-98 | S | Protein of unknown function (DUF3114) | |||
KDBJKIBH_01621 | 3.3e-94 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
KDBJKIBH_01622 | 1e-21 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
KDBJKIBH_01623 | 3.5e-70 | 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) | |
KDBJKIBH_01624 | 1.7e-204 | 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) | |
KDBJKIBH_01625 | 8.1e-88 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
KDBJKIBH_01626 | 3.5e-277 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KDBJKIBH_01628 | 1.1e-43 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KDBJKIBH_01629 | 1.5e-71 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KDBJKIBH_01630 | 9.1e-15 | ilvD | 4.2.1.9 | H | Dehydratase family | |
KDBJKIBH_01631 | 1.6e-09 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
KDBJKIBH_01632 | 9.5e-22 | yloV | S | kinase related to dihydroxyacetone kinase | ||
KDBJKIBH_01633 | 4.4e-101 | yloV | S | kinase related to dihydroxyacetone kinase | ||
KDBJKIBH_01634 | 4.7e-53 | yloV | S | kinase related to dihydroxyacetone kinase | ||
KDBJKIBH_01635 | 3.6e-77 | ogt | 2.1.1.63, 3.2.2.20 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
KDBJKIBH_01636 | 1.8e-167 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KDBJKIBH_01637 | 1.9e-63 | wecD | M | Acetyltransferase (GNAT) domain | ||
KDBJKIBH_01638 | 2.6e-07 | wecD | M | Acetyltransferase (GNAT) domain | ||
KDBJKIBH_01639 | 1.4e-170 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
KDBJKIBH_01640 | 5.8e-163 | murB | 1.3.1.98 | M | cell wall formation | |
KDBJKIBH_01641 | 4.2e-110 | 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 | |
KDBJKIBH_01642 | 2e-65 | 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 | |
KDBJKIBH_01643 | 7.9e-24 | mur1 | NU | mannosyl-glycoprotein | ||
KDBJKIBH_01645 | 1.1e-50 | nptA | P | sodium-dependent phosphate transmembrane transporter activity | ||
KDBJKIBH_01646 | 2.8e-21 | nptA | P | sodium-dependent phosphate transmembrane transporter activity | ||
KDBJKIBH_01647 | 7.1e-15 | nptA | P | sodium-dependent phosphate transmembrane transporter activity | ||
KDBJKIBH_01648 | 5.2e-220 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
KDBJKIBH_01649 | 2e-15 | |||||
KDBJKIBH_01650 | 1.1e-106 | L | Phage integrase family | |||
KDBJKIBH_01651 | 8.8e-16 | |||||
KDBJKIBH_01652 | 3.1e-40 | isp2 | S | pathogenesis | ||
KDBJKIBH_01654 | 4.7e-241 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
KDBJKIBH_01655 | 1.4e-69 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
KDBJKIBH_01656 | 3.7e-94 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
KDBJKIBH_01657 | 3.5e-32 | ysdA | L | Membrane | ||
KDBJKIBH_01658 | 4.1e-18 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KDBJKIBH_01659 | 3.2e-12 | leuC | 4.2.1.33, 4.2.1.35 | H | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
KDBJKIBH_01660 | 4.5e-09 | pbuO | S | permease | ||
KDBJKIBH_01661 | 1.6e-77 | pbuO | S | permease | ||
KDBJKIBH_01662 | 1e-30 | pbuO | S | permease | ||
KDBJKIBH_01663 | 5.9e-95 | pbuO | S | permease | ||
KDBJKIBH_01664 | 4.6e-39 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
KDBJKIBH_01665 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
KDBJKIBH_01666 | 2.8e-37 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
KDBJKIBH_01667 | 2e-69 | smpB | O | 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 | ||
KDBJKIBH_01669 | 1.9e-48 | yjbB | G | Permeases of the major facilitator superfamily | ||
KDBJKIBH_01670 | 9.4e-79 | yjbB | G | Permeases of the major facilitator superfamily | ||
KDBJKIBH_01671 | 1.5e-258 | 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 | ||
KDBJKIBH_01672 | 1.3e-18 | 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 | ||
KDBJKIBH_01673 | 3.3e-124 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
KDBJKIBH_01674 | 1.7e-70 | sptS | 2.7.13.3 | T | Histidine kinase | |
KDBJKIBH_01675 | 1.2e-13 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_01676 | 5.5e-30 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_01677 | 3.6e-86 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_01678 | 7.6e-46 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_01679 | 1.1e-36 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_01680 | 4.3e-114 | yeiH | S | Membrane | ||
KDBJKIBH_01681 | 4.6e-17 | mur1 | NU | muramidase | ||
KDBJKIBH_01682 | 6.8e-81 | mur1 | NU | amidase activity | ||
KDBJKIBH_01683 | 1e-18 | L | transposase activity | |||
KDBJKIBH_01684 | 3.5e-72 | L | transposition | |||
KDBJKIBH_01685 | 5.6e-68 | macB2 | V | ABC transporter, ATP-binding protein | ||
KDBJKIBH_01686 | 2.5e-28 | macB2 | V | ABC transporter, ATP-binding protein | ||
KDBJKIBH_01687 | 1.3e-69 | V | ABC transporter (permease) | |||
KDBJKIBH_01688 | 1.3e-20 | V | ABC transporter (permease) | |||
KDBJKIBH_01689 | 3.1e-86 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
KDBJKIBH_01690 | 1.1e-57 | 2.7.1.199, 2.7.1.211 | G | PTS glucose transporter subunit IIA | ||
KDBJKIBH_01691 | 1e-27 | pts33BCA | G | pts system | ||
KDBJKIBH_01692 | 6.6e-48 | pts33BCA | G | pts system | ||
KDBJKIBH_01693 | 5.8e-71 | pts33BCA | G | pts system | ||
KDBJKIBH_01694 | 2.8e-24 | 2.7.1.208, 2.7.1.211 | G | protein-N(PI)-phosphohistidine-sugar phosphotransferase activity | ||
KDBJKIBH_01696 | 7.6e-35 | XK27_05000 | S | metal cluster binding | ||
KDBJKIBH_01697 | 8.4e-177 | V | ABC transporter (permease) | |||
KDBJKIBH_01698 | 2.9e-34 | V | ABC transporter (permease) | |||
KDBJKIBH_01699 | 9.5e-141 | lmrA2 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01700 | 1.2e-36 | K | Acetyltransferase (GNAT) family | |||
KDBJKIBH_01701 | 3.7e-20 | sptS | 2.7.13.3 | T | Histidine kinase | |
KDBJKIBH_01702 | 1.5e-21 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
KDBJKIBH_01703 | 1.9e-77 | K | DNA-binding transcription factor activity | |||
KDBJKIBH_01704 | 5e-32 | lmrA1 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01705 | 3.6e-20 | lmrA1 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01706 | 4.9e-106 | lmrA1 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01707 | 3.8e-45 | lmrA1 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01708 | 3.4e-38 | lmrA2 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01709 | 6.1e-15 | lmrA2 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01710 | 1.4e-25 | lmrA2 | V | abc transporter atp-binding protein | ||
KDBJKIBH_01711 | 5.7e-29 | manL | 2.7.1.191 | G | pts system | |
KDBJKIBH_01712 | 9.4e-79 | manL | 2.7.1.191 | G | pts system | |
KDBJKIBH_01713 | 9.5e-129 | XK27_00940 | 1.2.1.70, 3.5.1.9 | S | Metal-dependent hydrolase | |
KDBJKIBH_01714 | 3.2e-21 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
KDBJKIBH_01715 | 4.1e-57 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
KDBJKIBH_01716 | 2.5e-84 | pstS | P | phosphate | ||
KDBJKIBH_01717 | 1.6e-22 | pstS | P | phosphate | ||
KDBJKIBH_01718 | 2.8e-64 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
KDBJKIBH_01719 | 8.6e-133 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
KDBJKIBH_01720 | 1.2e-13 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
KDBJKIBH_01721 | 8.6e-47 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
KDBJKIBH_01722 | 1.3e-112 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
KDBJKIBH_01723 | 3e-128 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
KDBJKIBH_01724 | 2.6e-28 | 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 | ||
KDBJKIBH_01725 | 2.5e-40 | 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 | ||
KDBJKIBH_01728 | 1.2e-32 | 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 |
KDBJKIBH_01729 | 1.3e-224 | 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 |
KDBJKIBH_01730 | 1.6e-120 | 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 | |
KDBJKIBH_01731 | 1.8e-116 | 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 | ||
KDBJKIBH_01732 | 2.3e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
KDBJKIBH_01733 | 5.8e-28 | M | LysM domain | |||
KDBJKIBH_01734 | 1e-45 | M | LysM domain | |||
KDBJKIBH_01735 | 2.3e-139 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
KDBJKIBH_01736 | 1.1e-93 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
KDBJKIBH_01737 | 2.2e-79 | alkD | L | Dna alkylation repair | ||
KDBJKIBH_01738 | 2.2e-31 | pat | 2.3.1.183 | M | acetyltransferase | |
KDBJKIBH_01739 | 1.1e-31 | pat | 2.3.1.183 | M | acetyltransferase | |
KDBJKIBH_01740 | 1e-25 | K | hmm pf08876 | |||
KDBJKIBH_01741 | 6.5e-96 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
KDBJKIBH_01742 | 9.9e-22 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
KDBJKIBH_01743 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
KDBJKIBH_01744 | 1.1e-127 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
KDBJKIBH_01745 | 6.2e-24 | WQ51_03320 | S | cog cog4835 | ||
KDBJKIBH_01748 | 6.6e-42 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_01749 | 5.4e-27 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
KDBJKIBH_01750 | 3.4e-42 | T | PhoQ Sensor | |||
KDBJKIBH_01751 | 1.9e-53 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KDBJKIBH_01752 | 5e-87 | S | TraX protein | |||
KDBJKIBH_01753 | 2.6e-51 | S | TraX protein | |||
KDBJKIBH_01754 | 5.7e-186 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
KDBJKIBH_01755 | 1.5e-136 | 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 | |
KDBJKIBH_01756 | 6.3e-114 | pstA | P | phosphate transport system permease | ||
KDBJKIBH_01757 | 4.2e-22 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KDBJKIBH_01758 | 1.9e-15 | ybbR | S | Protein conserved in bacteria | ||
KDBJKIBH_01759 | 4.4e-141 | ybbR | S | Protein conserved in bacteria | ||
KDBJKIBH_01760 | 7.8e-28 | acmA | 3.2.1.17 | NU | amidase activity | |
KDBJKIBH_01761 | 8.7e-48 | acmA | 3.2.1.17 | NU | amidase activity | |
KDBJKIBH_01762 | 2.3e-87 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
KDBJKIBH_01763 | 2.8e-230 | ftsW | D | Belongs to the SEDS family | ||
KDBJKIBH_01764 | 3.7e-19 | XK27_05745 | ||||
KDBJKIBH_01765 | 9.5e-10 | XK27_05745 | ||||
KDBJKIBH_01766 | 2.5e-27 | ptsG | 2.7.1.199, 2.7.1.208 | G | pts system | |
KDBJKIBH_01767 | 3e-23 | ptsG | 2.7.1.199, 2.7.1.208 | G | pts system | |
KDBJKIBH_01768 | 7.1e-28 | ptsG | 2.7.1.199, 2.7.1.208 | G | pts system | |
KDBJKIBH_01769 | 4.2e-44 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | pts system | |
KDBJKIBH_01770 | 1.2e-33 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | pts system | |
KDBJKIBH_01771 | 1.6e-150 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
KDBJKIBH_01772 | 5.8e-14 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
KDBJKIBH_01773 | 3.4e-13 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
KDBJKIBH_01774 | 2.1e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KDBJKIBH_01775 | 6.2e-58 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KDBJKIBH_01776 | 4.4e-44 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KDBJKIBH_01777 | 1.1e-200 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
KDBJKIBH_01779 | 7.5e-157 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
KDBJKIBH_01780 | 1.5e-84 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |
KDBJKIBH_01781 | 1.1e-165 | brpA | K | Transcriptional | ||
KDBJKIBH_01782 | 9.3e-92 | XK27_05885 | 2.3.1.82 | M | Acetyltransferase GNAT Family | |
KDBJKIBH_01783 | 1.5e-118 | 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 | |
KDBJKIBH_01784 | 7.3e-26 | 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 | |
KDBJKIBH_01785 | 9.6e-13 | 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 | |
KDBJKIBH_01786 | 2.4e-41 | 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 | |
KDBJKIBH_01787 | 1.1e-18 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
KDBJKIBH_01788 | 6.9e-133 | 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 | |
KDBJKIBH_01790 | 6.9e-73 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
KDBJKIBH_01791 | 2e-26 | ywaF | S | Integral membrane protein (intg_mem_TP0381) | ||
KDBJKIBH_01792 | 1.6e-20 | 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 | ||
KDBJKIBH_01793 | 7.3e-130 | pacL | 3.6.3.8 | P | cation transport ATPase | |
KDBJKIBH_01794 | 2.4e-153 | corA | P | COG0598 Mg2 and Co2 transporters | ||
KDBJKIBH_01795 | 5.5e-12 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
KDBJKIBH_01796 | 4.5e-26 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
KDBJKIBH_01797 | 5.5e-52 | S | phosphatase activity | |||
KDBJKIBH_01798 | 4.9e-19 | rrmA | 2.1.1.187 | Q | methyltransferase | |
KDBJKIBH_01799 | 1.4e-35 | 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 | |
KDBJKIBH_01800 | 3.7e-41 | nrdI | F | Belongs to the NrdI family | ||
KDBJKIBH_01801 | 5.9e-52 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KDBJKIBH_01802 | 6e-137 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
KDBJKIBH_01803 | 3.2e-88 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
KDBJKIBH_01804 | 3.7e-174 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
KDBJKIBH_01805 | 2.7e-45 | ylbG | S | UPF0298 protein | ||
KDBJKIBH_01806 | 5.6e-62 | ylbF | S | Belongs to the UPF0342 family | ||
KDBJKIBH_01807 | 7.7e-49 | usp | 3.5.1.104, 3.5.1.28 | CBM50 | S | pathogenesis |
KDBJKIBH_01808 | 8.7e-32 | 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 | ||
KDBJKIBH_01809 | 4.4e-152 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
KDBJKIBH_01810 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
KDBJKIBH_01811 | 1e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
KDBJKIBH_01812 | 1.9e-29 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
KDBJKIBH_01813 | 5.2e-26 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KDBJKIBH_01814 | 8.7e-162 | whiA | K | May be required for sporulation | ||
KDBJKIBH_01815 | 1.1e-219 | 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 | |
KDBJKIBH_01816 | 4.7e-188 | 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 | |
KDBJKIBH_01817 | 5.3e-47 | veg | S | Biofilm formation stimulator VEG | ||
KDBJKIBH_01819 | 2.8e-48 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
KDBJKIBH_01820 | 1.6e-13 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
KDBJKIBH_01821 | 1.9e-33 | K | transcriptional regulator, MerR family | |||
KDBJKIBH_01822 | 8.3e-61 | mdlB | V | abc transporter atp-binding protein | ||
KDBJKIBH_01823 | 1.1e-167 | lmrA | V | abc transporter atp-binding protein | ||
KDBJKIBH_01825 | 6.6e-90 | 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 | ||
KDBJKIBH_01826 | 9.7e-36 | 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 | ||
KDBJKIBH_01828 | 2e-82 | 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 | |
KDBJKIBH_01829 | 3.4e-108 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
KDBJKIBH_01830 | 3.8e-42 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
KDBJKIBH_01831 | 1.3e-72 | S | Haloacid dehalogenase-like hydrolase | |||
KDBJKIBH_01832 | 5.6e-95 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KDBJKIBH_01833 | 8.8e-79 | EGP | Major facilitator Superfamily | |||
KDBJKIBH_01834 | 1.2e-27 | KLT | serine threonine protein kinase | |||
KDBJKIBH_01835 | 1e-34 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KDBJKIBH_01836 | 2.2e-41 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
KDBJKIBH_01837 | 4.9e-84 | rapZ | S | Displays ATPase and GTPase activities | ||
KDBJKIBH_01838 | 9.2e-38 | rapZ | S | Displays ATPase and GTPase activities | ||
KDBJKIBH_01839 | 2.2e-58 | yejC | S | cyclic nucleotide-binding protein | ||
KDBJKIBH_01840 | 1.9e-187 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
KDBJKIBH_01841 | 8.4e-134 | 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 | ||
KDBJKIBH_01842 | 2.9e-169 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
KDBJKIBH_01843 | 2.7e-42 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
KDBJKIBH_01844 | 1.3e-38 | L | transposase activity | |||
KDBJKIBH_01845 | 2.8e-22 | L | transposase activity | |||
KDBJKIBH_01846 | 5.1e-27 | L | transposition | |||
KDBJKIBH_01847 | 3.3e-68 | ureI | S | AmiS/UreI family transporter | ||
KDBJKIBH_01848 | 3e-29 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
KDBJKIBH_01849 | 1.5e-08 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
KDBJKIBH_01852 | 1.7e-182 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
KDBJKIBH_01853 | 1e-84 | L | PFAM Integrase catalytic region | |||
KDBJKIBH_01854 | 3.1e-36 | XK27_00115 | 2.3.1.128 | K | Acetyltransferase GNAT family | |
KDBJKIBH_01856 | 2.5e-23 | 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 | |
KDBJKIBH_01857 | 6.1e-88 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
KDBJKIBH_01858 | 2.7e-120 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
KDBJKIBH_01859 | 2.4e-11 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KDBJKIBH_01860 | 1.5e-83 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KDBJKIBH_01861 | 1.3e-31 | L | Integrase core domain protein | |||
KDBJKIBH_01862 | 1.2e-52 | vraS | 2.7.13.3 | T | Histidine kinase | |
KDBJKIBH_01863 | 3.3e-69 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
KDBJKIBH_01864 | 4.2e-36 | yccU | S | CoA-binding protein | ||
KDBJKIBH_01865 | 1.5e-45 | argR | K | arginine binding | ||
KDBJKIBH_01866 | 2e-59 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KDBJKIBH_01867 | 5.6e-128 | 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 | ||
KDBJKIBH_01868 | 2.4e-56 | 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 | |
KDBJKIBH_01869 | 5.7e-34 | 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 | |
KDBJKIBH_01870 | 1.1e-95 | 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 | |
KDBJKIBH_01871 | 2.6e-29 | 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 | |
KDBJKIBH_01872 | 5.2e-139 | 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 | ||
KDBJKIBH_01873 | 4.6e-45 | 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) | |
KDBJKIBH_01874 | 3.7e-28 | amiA | E | transmembrane transport | ||
KDBJKIBH_01875 | 1.3e-16 | XK27_08635 | S | UPF0210 protein | ||
KDBJKIBH_01876 | 1.2e-10 | XK27_08635 | S | UPF0210 protein | ||
KDBJKIBH_01877 | 6.8e-39 | XK27_08635 | S | UPF0210 protein | ||
KDBJKIBH_01878 | 6.3e-24 | 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 | ||
KDBJKIBH_01881 | 1.2e-19 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
KDBJKIBH_01882 | 3e-39 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
KDBJKIBH_01883 | 1.1e-69 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
KDBJKIBH_01884 | 7.3e-30 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
KDBJKIBH_01885 | 8e-49 | G | Belongs to the phosphoglycerate mutase family | |||
KDBJKIBH_01886 | 3.3e-17 | supH | 3.1.3.102, 3.1.3.104 | Q | phosphatase activity | |
KDBJKIBH_01887 | 2.3e-24 | supH | 3.1.3.102, 3.1.3.104 | Q | phosphatase activity | |
KDBJKIBH_01888 | 3.2e-15 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
KDBJKIBH_01889 | 1.9e-08 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
KDBJKIBH_01890 | 2.4e-15 | M | transferase activity, transferring glycosyl groups | |||
KDBJKIBH_01891 | 7.3e-40 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
KDBJKIBH_01892 | 2.3e-45 | gadC | E | Psort location CytoplasmicMembrane, score 10.00 | ||
KDBJKIBH_01893 | 1.5e-24 | pepV | 3.5.1.18 | E | Dipeptidase | |
KDBJKIBH_01894 | 1.3e-90 | pepV | 3.5.1.18 | E | Dipeptidase | |
KDBJKIBH_01895 | 7.5e-44 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
KDBJKIBH_01896 | 7.1e-08 | yhbY | J | RNA-binding protein | ||
KDBJKIBH_01897 | 3.7e-151 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
KDBJKIBH_01898 | 6.8e-50 | DegV | S | DegV family | ||
KDBJKIBH_01899 | 3e-108 | recN | L | May be involved in recombinational repair of damaged DNA | ||
KDBJKIBH_01900 | 6.2e-85 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KDBJKIBH_01901 | 4.6e-61 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KDBJKIBH_01903 | 2.1e-74 | S | QueT transporter | |||
KDBJKIBH_01904 | 2.9e-55 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
KDBJKIBH_01905 | 8.7e-34 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KDBJKIBH_01906 | 3.7e-39 | T | PhoQ Sensor | |||
KDBJKIBH_01907 | 5.4e-32 | cspD | K | Cold shock protein domain | ||
KDBJKIBH_01908 | 1.4e-37 | pepD | E | Dipeptidase | ||
KDBJKIBH_01909 | 2e-109 | pepD | E | Dipeptidase | ||
KDBJKIBH_01910 | 5.8e-28 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
KDBJKIBH_01911 | 5.7e-55 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
KDBJKIBH_01912 | 7.7e-25 | ftsE | D | cell division ATP-binding protein FtsE | ||
KDBJKIBH_01913 | 7.9e-17 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
KDBJKIBH_01914 | 8.4e-196 | ylbL | T | Belongs to the peptidase S16 family | ||
KDBJKIBH_01915 | 1e-20 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
KDBJKIBH_01916 | 1.7e-85 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
KDBJKIBH_01917 | 2.8e-106 | 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 | ||
KDBJKIBH_01918 | 2.3e-08 | 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 | ||
KDBJKIBH_01919 | 2.1e-50 | K | response regulator | |||
KDBJKIBH_01920 | 4.8e-30 | S | Signal peptide protein, YSIRK family | |||
KDBJKIBH_01921 | 1.8e-104 | K | Transcriptional regulator, TetR family | |||
KDBJKIBH_01922 | 2.2e-148 | cpsY | K | Transcriptional regulator | ||
KDBJKIBH_01923 | 7.5e-49 | hlpA | M | Belongs to the NlpA lipoprotein family | ||
KDBJKIBH_01924 | 2e-30 | hlpA | M | Belongs to the NlpA lipoprotein family | ||
KDBJKIBH_01925 | 7.7e-14 | hlpA | M | Belongs to the NlpA lipoprotein family | ||
KDBJKIBH_01926 | 4.2e-50 | dtpT | E | transporter | ||
KDBJKIBH_01927 | 8.2e-41 | L | Transposase | |||
KDBJKIBH_01928 | 1.5e-71 | 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 | |
KDBJKIBH_01929 | 1.8e-66 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
KDBJKIBH_01930 | 2.3e-151 | ytoI | K | transcriptional regulator containing CBS domains | ||
KDBJKIBH_01931 | 2.7e-53 | P | ABC transporter (Permease | |||
KDBJKIBH_01932 | 1.1e-63 | papP | P | ABC transporter (Permease | ||
KDBJKIBH_01933 | 1.7e-28 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
KDBJKIBH_01934 | 4.1e-118 | yubA | S | permease | ||
KDBJKIBH_01935 | 4.3e-37 | G | COG0457 FOG TPR repeat | |||
KDBJKIBH_01936 | 1.8e-48 | G | COG0457 FOG TPR repeat | |||
KDBJKIBH_01937 | 2.3e-29 | mutX | 3.6.1.55 | F | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
KDBJKIBH_01938 | 2.7e-45 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
KDBJKIBH_01939 | 1.6e-31 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
KDBJKIBH_01940 | 6.3e-18 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
KDBJKIBH_01941 | 1.3e-29 | 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 | |
KDBJKIBH_01942 | 7.7e-121 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
KDBJKIBH_01943 | 6.4e-22 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
KDBJKIBH_01944 | 2.5e-62 | yjqA | S | Bacterial PH domain | ||
KDBJKIBH_01945 | 2e-84 | corA | P | CorA-like protein | ||
KDBJKIBH_01946 | 1.1e-131 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
KDBJKIBH_01947 | 1.6e-64 | cycA | E | permease | ||
KDBJKIBH_01948 | 2e-62 | cycA | E | permease | ||
KDBJKIBH_01949 | 1.3e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
KDBJKIBH_01950 | 7.4e-15 | 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 | ||
KDBJKIBH_01951 | 6.2e-103 | 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 | ||
KDBJKIBH_01952 | 3.6e-32 | 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 | ||
KDBJKIBH_01954 | 9.8e-155 | ylbM | S | Belongs to the UPF0348 family | ||
KDBJKIBH_01955 | 2.6e-129 | 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 | |
KDBJKIBH_01956 | 1.5e-109 | scrB | 3.2.1.26 | GH32 | G | invertase |
KDBJKIBH_01957 | 9.1e-13 | V | Glucan-binding protein C | |||
KDBJKIBH_01958 | 9.1e-34 | mdlB | V | abc transporter atp-binding protein | ||
KDBJKIBH_01960 | 1.4e-108 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
KDBJKIBH_01961 | 4.8e-17 | 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 | ||
KDBJKIBH_01962 | 3.7e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KDBJKIBH_01963 | 1.1e-45 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
KDBJKIBH_01964 | 2e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
KDBJKIBH_01965 | 9e-23 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
KDBJKIBH_01966 | 1.6e-32 | rplQ | J | ribosomal protein l17 | ||
KDBJKIBH_01967 | 1.2e-62 | L | PFAM Integrase, catalytic core | |||
KDBJKIBH_01968 | 4e-62 | S | Putative small multi-drug export protein | |||
KDBJKIBH_01969 | 1.8e-69 | 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 | ||
KDBJKIBH_01970 | 5.5e-20 | csbD | K | CsbD-like | ||
KDBJKIBH_01971 | 8.1e-18 | GK | ROK family | |||
KDBJKIBH_01972 | 3e-93 | GK | ROK family | |||
KDBJKIBH_01973 | 3.2e-181 | pacL | 3.6.3.8 | P | cation transport ATPase | |
KDBJKIBH_01974 | 8.1e-17 | pacL | 3.6.3.8 | P | cation transport ATPase | |
KDBJKIBH_01975 | 1.4e-58 | mutT | 3.6.1.55 | F | Nudix family | |
KDBJKIBH_01976 | 4.8e-97 | 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 | ||
KDBJKIBH_01977 | 3.4e-11 | 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 | ||
KDBJKIBH_01978 | 3.1e-33 | S | cog cog4699 | |||
KDBJKIBH_01979 | 9.1e-66 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KDBJKIBH_01980 | 2.4e-108 | mdtG | EGP | Major facilitator Superfamily | ||
KDBJKIBH_01982 | 1.1e-27 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
KDBJKIBH_01983 | 7.3e-78 | atpF | C | ATP synthase F(0) sector subunit b | ||
KDBJKIBH_01984 | 4e-57 | 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 | ||
KDBJKIBH_01986 | 8.7e-44 | XK27_08635 | S | UPF0210 protein | ||
KDBJKIBH_01987 | 1.6e-31 | ais | G | Phosphoglycerate mutase | ||
KDBJKIBH_01988 | 4e-26 | ais | G | alpha-ribazole phosphatase activity | ||
KDBJKIBH_01989 | 3.2e-57 | |||||
KDBJKIBH_01990 | 5.7e-47 | azlD | E | branched-chain amino acid | ||
KDBJKIBH_01991 | 1.3e-44 | azlC | E | AzlC protein | ||
KDBJKIBH_01992 | 3.2e-78 | scrA | 2.7.1.208, 2.7.1.211 | G | pts system | |
KDBJKIBH_01993 | 2.8e-108 | 3.1.3.18 | S | IA, variant 1 | ||
KDBJKIBH_01994 | 2.8e-77 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
KDBJKIBH_01995 | 2.4e-17 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
KDBJKIBH_01996 | 4.7e-45 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
KDBJKIBH_01997 | 3.9e-81 | aatB | ET | ABC transporter substrate-binding protein | ||
KDBJKIBH_01998 | 2.2e-71 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
KDBJKIBH_01999 | 3.1e-34 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
KDBJKIBH_02000 | 1.4e-32 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
KDBJKIBH_02001 | 6.8e-27 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KDBJKIBH_02002 | 2.1e-24 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
KDBJKIBH_02003 | 6.9e-102 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KDBJKIBH_02004 | 3.4e-45 | 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 | |
KDBJKIBH_02005 | 2e-40 | 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 | |
KDBJKIBH_02006 | 1.3e-80 | artQ | P | ABC transporter (Permease | ||
KDBJKIBH_02007 | 1.3e-23 | cmpC | S | abc transporter atp-binding protein | ||
KDBJKIBH_02008 | 7.6e-50 | cmpC | S | abc transporter atp-binding protein | ||
KDBJKIBH_02009 | 1.3e-26 | 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 | ||
KDBJKIBH_02010 | 7.8e-60 | V | VanZ like family | |||
KDBJKIBH_02011 | 2.5e-58 | ypsA | S | Belongs to the UPF0398 family | ||
KDBJKIBH_02012 | 2.7e-62 | XK27_02560 | S | cog cog2151 | ||
KDBJKIBH_02013 | 4.7e-103 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
KDBJKIBH_02014 | 1.9e-13 | |||||
KDBJKIBH_02015 | 9.6e-41 | 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 | ||
KDBJKIBH_02016 | 1.4e-20 | 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 | ||
KDBJKIBH_02017 | 6.3e-52 | 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 | ||
KDBJKIBH_02018 | 7.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
KDBJKIBH_02019 | 3.1e-63 | cvfB | S | Protein conserved in bacteria | ||
KDBJKIBH_02020 | 3.5e-42 | 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 | ||
KDBJKIBH_02021 | 1.2e-36 | 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 | ||
KDBJKIBH_02022 | 1e-12 | 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 | ||
KDBJKIBH_02023 | 8.2e-91 | rssA | S | Phospholipase, patatin family | ||
KDBJKIBH_02024 | 2.5e-59 | estA | E | GDSL-like protein | ||
KDBJKIBH_02025 | 1.4e-43 | |||||
KDBJKIBH_02026 | 2e-10 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
KDBJKIBH_02027 | 9.5e-25 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
KDBJKIBH_02028 | 2.1e-17 | 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 | |
KDBJKIBH_02029 | 6.7e-22 | 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 | |
KDBJKIBH_02030 | 5.2e-25 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
KDBJKIBH_02031 | 4.6e-39 | trxA | O | Belongs to the thioredoxin family | ||
KDBJKIBH_02032 | 1.2e-89 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
KDBJKIBH_02033 | 2.7e-61 | glnP | P | ABC transporter | ||
KDBJKIBH_02034 | 6.7e-44 | glnQ | E | abc transporter atp-binding protein | ||
KDBJKIBH_02035 | 1.4e-23 | 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 | |
KDBJKIBH_02036 | 3.4e-109 | XK27_07020 | S | Belongs to the UPF0371 family | ||
KDBJKIBH_02037 | 2.1e-48 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
KDBJKIBH_02038 | 3.3e-61 | XK27_08050 | O | stress-induced mitochondrial fusion | ||
KDBJKIBH_02039 | 1.1e-18 | XK27_07020 | S | Belongs to the UPF0371 family | ||
KDBJKIBH_02040 | 7.4e-44 | XK27_07020 | S | Belongs to the UPF0371 family | ||
KDBJKIBH_02041 | 5.1e-65 | comEC | S | Competence protein ComEC | ||
KDBJKIBH_02042 | 4.9e-21 | XK27_13030 | ||||
KDBJKIBH_02043 | 4.1e-15 | 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 | |
KDBJKIBH_02044 | 2e-18 | potD | P | spermidine putrescine ABC transporter | ||
KDBJKIBH_02045 | 3.9e-61 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
KDBJKIBH_02046 | 2.9e-97 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
KDBJKIBH_02047 | 1.3e-52 | tcyB_2 | P | ABC transporter (permease) | ||
KDBJKIBH_02048 | 6.2e-21 | S | CAAX amino terminal protease family protein | |||
KDBJKIBH_02049 | 1.2e-85 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
KDBJKIBH_02050 | 6.3e-71 | potD | P | spermidine putrescine ABC transporter | ||
KDBJKIBH_02051 | 8.2e-32 | potD | P | spermidine putrescine ABC transporter | ||
KDBJKIBH_02052 | 3.4e-25 | S | Domain of unknown function (DUF4081) | |||
KDBJKIBH_02053 | 4.3e-107 | dtpT | E | transporter | ||
KDBJKIBH_02054 | 5.4e-28 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
KDBJKIBH_02055 | 2.8e-27 | S | UPF0397 protein | |||
KDBJKIBH_02056 | 8.2e-14 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
KDBJKIBH_02057 | 7.9e-40 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
KDBJKIBH_02058 | 2.9e-90 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
KDBJKIBH_02059 | 3.1e-09 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
KDBJKIBH_02060 | 7e-65 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
KDBJKIBH_02061 | 3.9e-119 | 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 | ||
KDBJKIBH_02063 | 1e-93 | 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 | ||
KDBJKIBH_02064 | 8.5e-54 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KDBJKIBH_02065 | 6.3e-97 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KDBJKIBH_02066 | 2.5e-17 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
KDBJKIBH_02067 | 1.8e-12 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
KDBJKIBH_02068 | 6.2e-42 | pchB | 2.5.1.19, 4.2.1.10, 4.2.99.21, 5.4.99.5 | E | Chorismate mutase | |
KDBJKIBH_02069 | 2.2e-40 | 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 | ||
KDBJKIBH_02070 | 3.3e-95 | 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 | ||
KDBJKIBH_02071 | 6.3e-28 | |||||
KDBJKIBH_02072 | 2.2e-57 | Q | phosphatase activity | |||
KDBJKIBH_02073 | 2.4e-27 | S | haloacid dehalogenase-like hydrolase | |||
KDBJKIBH_02075 | 1.3e-08 | L | thioesterase | |||
KDBJKIBH_02076 | 1.5e-64 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
KDBJKIBH_02077 | 2.7e-17 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
KDBJKIBH_02078 | 2.5e-50 | WQ51_06230 | S | ABC transporter substrate binding protein | ||
KDBJKIBH_02079 | 4.1e-07 | WQ51_06230 | S | ABC transporter substrate binding protein | ||
KDBJKIBH_02080 | 5e-24 | WQ51_06230 | S | ABC transporter substrate binding protein | ||
KDBJKIBH_02081 | 9.5e-121 | 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 | |
KDBJKIBH_02082 | 1.3e-45 | glnQ | E | abc transporter atp-binding protein | ||
KDBJKIBH_02083 | 9.1e-44 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
KDBJKIBH_02084 | 2.4e-130 | XK27_02985 | S | overlaps another CDS with the same product name | ||
KDBJKIBH_02085 | 9.6e-15 | 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 | ||
KDBJKIBH_02086 | 1.7e-07 | 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 | ||
KDBJKIBH_02087 | 4.8e-132 | 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 | ||
KDBJKIBH_02088 | 2.3e-44 | yktA | S | Belongs to the UPF0223 family | ||
KDBJKIBH_02089 | 4.2e-116 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
KDBJKIBH_02090 | 2.2e-17 | lrgA | S | Effector of murein hydrolase LrgA | ||
KDBJKIBH_02091 | 2e-24 | lrgB | M | effector of murein hydrolase | ||
KDBJKIBH_02092 | 1.6e-17 | lrgB | M | effector of murein hydrolase | ||
KDBJKIBH_02093 | 2.3e-66 | pepV | 3.5.1.18 | E | Dipeptidase | |
KDBJKIBH_02094 | 3.8e-93 | 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 | ||
KDBJKIBH_02095 | 2.2e-48 | yclP | 3.6.3.34 | P | abc transporter atp-binding protein | |
KDBJKIBH_02096 | 1.1e-28 | fatB | P | ABC-type enterochelin transport system, periplasmic component | ||
KDBJKIBH_02097 | 1.8e-50 | 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 | |
KDBJKIBH_02098 | 1.7e-29 | atpB | C | it plays a direct role in the translocation of protons across the membrane |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)