ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
KJBOBAIK_00001 | 9.4e-177 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
KJBOBAIK_00002 | 3.4e-63 | yjcE | P | NhaP-type Na H and K H | ||
KJBOBAIK_00003 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
KJBOBAIK_00004 | 6.4e-143 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
KJBOBAIK_00005 | 3.8e-235 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
KJBOBAIK_00006 | 2.9e-76 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KJBOBAIK_00007 | 2e-189 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
KJBOBAIK_00008 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
KJBOBAIK_00009 | 3.5e-75 | |||||
KJBOBAIK_00010 | 2.3e-181 | M | CHAP domain | |||
KJBOBAIK_00011 | 1.5e-264 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
KJBOBAIK_00012 | 8.5e-60 | |||||
KJBOBAIK_00014 | 6.5e-44 | |||||
KJBOBAIK_00015 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
KJBOBAIK_00016 | 8.3e-168 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
KJBOBAIK_00017 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
KJBOBAIK_00018 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KJBOBAIK_00019 | 8.9e-37 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KJBOBAIK_00020 | 7.9e-177 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KJBOBAIK_00021 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KJBOBAIK_00022 | 1.2e-57 | FbpA | K | Fibronectin-binding protein | ||
KJBOBAIK_00023 | 1.5e-236 | FbpA | K | Fibronectin-binding protein | ||
KJBOBAIK_00024 | 1.1e-66 | |||||
KJBOBAIK_00025 | 1e-159 | degV | S | EDD domain protein, DegV family | ||
KJBOBAIK_00026 | 1.4e-125 | S | PAS domain | |||
KJBOBAIK_00027 | 1.6e-11 | |||||
KJBOBAIK_00029 | 8.8e-159 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KJBOBAIK_00030 | 4.3e-86 | 3.4.21.96 | S | SLAP domain | ||
KJBOBAIK_00031 | 3.6e-174 | ycaM | E | amino acid | ||
KJBOBAIK_00032 | 3.1e-139 | S | Cysteine-rich secretory protein family | |||
KJBOBAIK_00033 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
KJBOBAIK_00034 | 8e-258 | lmrB | EGP | Major facilitator Superfamily | ||
KJBOBAIK_00035 | 3.1e-48 | S | Domain of unknown function (DUF4811) | |||
KJBOBAIK_00036 | 2.2e-93 | 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 | ||
KJBOBAIK_00037 | 2e-194 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
KJBOBAIK_00038 | 6.8e-220 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
KJBOBAIK_00039 | 7.7e-103 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
KJBOBAIK_00040 | 2.4e-96 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
KJBOBAIK_00041 | 7e-45 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
KJBOBAIK_00042 | 6.5e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
KJBOBAIK_00043 | 4.1e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
KJBOBAIK_00044 | 1.4e-30 | |||||
KJBOBAIK_00045 | 9.9e-118 | L | Belongs to the 'phage' integrase family | |||
KJBOBAIK_00047 | 2.2e-15 | E | Pfam:DUF955 | |||
KJBOBAIK_00049 | 4.7e-18 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_00050 | 4.4e-79 | S | Phage antirepressor protein KilAC domain | |||
KJBOBAIK_00051 | 5.7e-31 | |||||
KJBOBAIK_00052 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
KJBOBAIK_00053 | 2.7e-124 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
KJBOBAIK_00054 | 1.3e-13 | |||||
KJBOBAIK_00055 | 1.2e-40 | rusA | 3.1.22.4 | L | Endodeoxyribonuclease RusA | |
KJBOBAIK_00061 | 9.3e-51 | dnaC | L | IstB-like ATP binding protein | ||
KJBOBAIK_00062 | 5.5e-35 | S | Conserved phage C-terminus (Phg_2220_C) | |||
KJBOBAIK_00063 | 1.8e-124 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
KJBOBAIK_00064 | 3.4e-94 | 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 | ||
KJBOBAIK_00065 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
KJBOBAIK_00066 | 2e-33 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
KJBOBAIK_00067 | 1.5e-24 | |||||
KJBOBAIK_00069 | 8.4e-10 | rnhA | 3.1.26.4 | L | Caulimovirus viroplasmin | |
KJBOBAIK_00070 | 4e-66 | |||||
KJBOBAIK_00071 | 1.7e-133 | 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) | |
KJBOBAIK_00072 | 9.1e-10 | UW | LPXTG-motif cell wall anchor domain protein | |||
KJBOBAIK_00073 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
KJBOBAIK_00074 | 1.2e-216 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
KJBOBAIK_00075 | 1e-141 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
KJBOBAIK_00076 | 2.5e-135 | ypuA | S | Protein of unknown function (DUF1002) | ||
KJBOBAIK_00077 | 8.8e-147 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
KJBOBAIK_00078 | 3.8e-181 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KJBOBAIK_00079 | 2.1e-42 | S | COG0790 FOG TPR repeat, SEL1 subfamily | |||
KJBOBAIK_00080 | 5.5e-38 | L | Protein of unknown function (DUF3991) | |||
KJBOBAIK_00084 | 3.7e-84 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
KJBOBAIK_00085 | 4.6e-129 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
KJBOBAIK_00087 | 1.6e-24 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
KJBOBAIK_00088 | 7e-14 | S | Repeat protein | |||
KJBOBAIK_00089 | 2.6e-78 | S | Repeat protein | |||
KJBOBAIK_00090 | 1.3e-76 | 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) | |
KJBOBAIK_00091 | 9.2e-275 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KJBOBAIK_00092 | 5.1e-75 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
KJBOBAIK_00098 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
KJBOBAIK_00099 | 2.1e-199 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
KJBOBAIK_00100 | 1.4e-176 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
KJBOBAIK_00101 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KJBOBAIK_00102 | 2.2e-97 | mtlR | K | Mga helix-turn-helix domain | ||
KJBOBAIK_00103 | 4.4e-151 | S | Metal-independent alpha-mannosidase (GH125) | |||
KJBOBAIK_00104 | 6e-73 | glnH | ET | ABC transporter substrate-binding protein | ||
KJBOBAIK_00105 | 3.7e-90 | gluC | P | ABC transporter permease | ||
KJBOBAIK_00106 | 4.7e-109 | glnP | P | ABC transporter permease | ||
KJBOBAIK_00107 | 1.1e-164 | S | Protein of unknown function (DUF2974) | |||
KJBOBAIK_00108 | 5.6e-86 | |||||
KJBOBAIK_00109 | 6.3e-212 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
KJBOBAIK_00110 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
KJBOBAIK_00111 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
KJBOBAIK_00112 | 8e-51 | L | RelB antitoxin | |||
KJBOBAIK_00113 | 4.5e-188 | S | Bacteriocin helveticin-J | |||
KJBOBAIK_00114 | 2.9e-145 | prmA | J | Ribosomal protein L11 methyltransferase | ||
KJBOBAIK_00115 | 8.2e-85 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
KJBOBAIK_00116 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
KJBOBAIK_00117 | 8.9e-114 | tnpB | L | Putative transposase DNA-binding domain | ||
KJBOBAIK_00118 | 1e-58 | tnpB | L | Putative transposase DNA-binding domain | ||
KJBOBAIK_00119 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
KJBOBAIK_00120 | 3.4e-111 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
KJBOBAIK_00121 | 1e-14 | 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 | |
KJBOBAIK_00122 | 3.1e-112 | 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 | |
KJBOBAIK_00123 | 2.3e-102 | S | Iron-sulfur cluster assembly protein | |||
KJBOBAIK_00124 | 8.5e-83 | yniG | EGP | Major facilitator Superfamily | ||
KJBOBAIK_00125 | 6.7e-109 | S | cog cog1373 | |||
KJBOBAIK_00126 | 7e-24 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
KJBOBAIK_00127 | 1.8e-307 | yjbQ | P | TrkA C-terminal domain protein | ||
KJBOBAIK_00128 | 2.5e-179 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
KJBOBAIK_00129 | 5.4e-215 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
KJBOBAIK_00131 | 6.8e-131 | S | SLAP domain | |||
KJBOBAIK_00133 | 5.3e-41 | |||||
KJBOBAIK_00134 | 1.4e-76 | K | DNA-templated transcription, initiation | |||
KJBOBAIK_00135 | 1.1e-25 | |||||
KJBOBAIK_00136 | 2.6e-57 | L | An automated process has identified a potential problem with this gene model | |||
KJBOBAIK_00137 | 7.9e-16 | L | An automated process has identified a potential problem with this gene model | |||
KJBOBAIK_00139 | 1.2e-24 | 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system EIIA 2 | ||
KJBOBAIK_00140 | 3.7e-196 | gatC | G | PTS system sugar-specific permease component | ||
KJBOBAIK_00141 | 6.5e-18 | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
KJBOBAIK_00142 | 3.5e-57 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
KJBOBAIK_00143 | 8.3e-123 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
KJBOBAIK_00144 | 1.3e-49 | lacR | K | Transcriptional regulator | ||
KJBOBAIK_00145 | 2.8e-98 | lacR | K | Transcriptional regulator | ||
KJBOBAIK_00146 | 2.6e-35 | yaaA | S | S4 domain protein YaaA | ||
KJBOBAIK_00147 | 6.4e-148 | 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 | ||
KJBOBAIK_00148 | 7.2e-25 | 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 | ||
KJBOBAIK_00149 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
KJBOBAIK_00150 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
KJBOBAIK_00151 | 3.3e-69 | S | Short repeat of unknown function (DUF308) | |||
KJBOBAIK_00152 | 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 | ||
KJBOBAIK_00153 | 8e-22 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
KJBOBAIK_00154 | 5.4e-53 | hipB | K | sequence-specific DNA binding | ||
KJBOBAIK_00155 | 4.8e-42 | S | SnoaL-like domain | |||
KJBOBAIK_00156 | 0.0 | L | PLD-like domain | |||
KJBOBAIK_00157 | 1.3e-174 | |||||
KJBOBAIK_00158 | 2.8e-47 | lysM | M | LysM domain | ||
KJBOBAIK_00159 | 5.2e-08 | |||||
KJBOBAIK_00160 | 3e-89 | ntd | 2.4.2.6 | F | Nucleoside | |
KJBOBAIK_00161 | 8.6e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
KJBOBAIK_00162 | 1.7e-78 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
KJBOBAIK_00163 | 2e-14 | M | domain protein | |||
KJBOBAIK_00164 | 6.6e-38 | M | domain protein | |||
KJBOBAIK_00168 | 4.3e-48 | U | TraM recognition site of TraD and TraG | |||
KJBOBAIK_00169 | 2.2e-93 | sip | L | Belongs to the 'phage' integrase family | ||
KJBOBAIK_00170 | 2.1e-161 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
KJBOBAIK_00171 | 2.1e-130 | |||||
KJBOBAIK_00172 | 5.6e-114 | |||||
KJBOBAIK_00173 | 2.5e-132 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
KJBOBAIK_00174 | 1.4e-98 | G | Aldose 1-epimerase | |||
KJBOBAIK_00175 | 2.3e-201 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KJBOBAIK_00176 | 1.6e-111 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
KJBOBAIK_00177 | 0.0 | XK27_08315 | M | Sulfatase | ||
KJBOBAIK_00178 | 1.2e-241 | S | response to antibiotic | |||
KJBOBAIK_00179 | 4.9e-125 | |||||
KJBOBAIK_00180 | 6.5e-227 | 3.6.3.8 | P | P-type ATPase | ||
KJBOBAIK_00182 | 1.2e-134 | EGP | Major facilitator Superfamily | |||
KJBOBAIK_00183 | 3.9e-78 | 3.1.3.102, 3.1.3.104 | S | haloacid dehalogenase-like hydrolase | ||
KJBOBAIK_00184 | 2.8e-74 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KJBOBAIK_00185 | 2.6e-123 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
KJBOBAIK_00186 | 1.9e-216 | EGP | Major facilitator Superfamily | |||
KJBOBAIK_00187 | 2.4e-192 | ampC | V | Beta-lactamase | ||
KJBOBAIK_00188 | 1.5e-60 | glcU | U | sugar transport | ||
KJBOBAIK_00189 | 7.1e-46 | |||||
KJBOBAIK_00190 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
KJBOBAIK_00191 | 1.9e-83 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
KJBOBAIK_00192 | 4.7e-38 | |||||
KJBOBAIK_00193 | 3.3e-183 | 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) | |
KJBOBAIK_00194 | 8.4e-125 | luxT | K | Bacterial regulatory proteins, tetR family | ||
KJBOBAIK_00195 | 2.8e-135 | |||||
KJBOBAIK_00196 | 1.6e-58 | glnPH2 | P | ABC transporter permease | ||
KJBOBAIK_00197 | 6.1e-158 | glnPH2 | P | ABC transporter permease | ||
KJBOBAIK_00198 | 7.1e-130 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KJBOBAIK_00199 | 6.3e-174 | S | Cysteine-rich secretory protein family | |||
KJBOBAIK_00200 | 3.8e-61 | S | Peptidase M16 | |||
KJBOBAIK_00201 | 2.9e-44 | S | Peptidase M16 | |||
KJBOBAIK_00202 | 1.1e-130 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
KJBOBAIK_00203 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
KJBOBAIK_00204 | 1.5e-92 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
KJBOBAIK_00205 | 1.7e-84 | pepA | E | M42 glutamyl aminopeptidase | ||
KJBOBAIK_00206 | 2.2e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
KJBOBAIK_00207 | 5.9e-174 | S | Aldo keto reductase | |||
KJBOBAIK_00208 | 1.4e-51 | |||||
KJBOBAIK_00209 | 1.1e-68 | |||||
KJBOBAIK_00210 | 2.4e-201 | steT | E | amino acid | ||
KJBOBAIK_00211 | 2.4e-26 | steT | E | amino acid | ||
KJBOBAIK_00212 | 2.5e-242 | steT | E | amino acid | ||
KJBOBAIK_00213 | 3.5e-128 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
KJBOBAIK_00214 | 4.2e-147 | glnH | ET | ABC transporter | ||
KJBOBAIK_00215 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
KJBOBAIK_00216 | 4.2e-306 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
KJBOBAIK_00217 | 0.0 | V | ABC transporter transmembrane region | |||
KJBOBAIK_00218 | 1.6e-100 | S | ABC-type cobalt transport system, permease component | |||
KJBOBAIK_00219 | 1e-246 | G | MFS/sugar transport protein | |||
KJBOBAIK_00220 | 1e-44 | udk | 2.7.1.48 | F | Zeta toxin | |
KJBOBAIK_00221 | 6.1e-44 | udk | 2.7.1.48 | F | Zeta toxin | |
KJBOBAIK_00222 | 4.2e-130 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KJBOBAIK_00223 | 4.9e-134 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
KJBOBAIK_00224 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
KJBOBAIK_00225 | 2.7e-75 | 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 | ||
KJBOBAIK_00226 | 1.6e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
KJBOBAIK_00227 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
KJBOBAIK_00229 | 6.3e-25 | srtA | 3.4.22.70 | M | sortase family | |
KJBOBAIK_00231 | 1.6e-24 | S | SLAP domain | |||
KJBOBAIK_00235 | 2.6e-11 | ssb | L | Single-strand binding protein family | ||
KJBOBAIK_00243 | 3.2e-24 | S | Domain of unknown function (DUF771) | |||
KJBOBAIK_00244 | 8.9e-32 | K | Helix-turn-helix domain | |||
KJBOBAIK_00245 | 1.2e-21 | XK27_07105 | K | Helix-turn-helix XRE-family like proteins | ||
KJBOBAIK_00246 | 1.2e-23 | K | Helix-turn-helix domain | |||
KJBOBAIK_00247 | 5e-08 | S | Pfam:DUF955 | |||
KJBOBAIK_00248 | 1.4e-153 | L | Belongs to the 'phage' integrase family | |||
KJBOBAIK_00250 | 1.2e-219 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KJBOBAIK_00251 | 5.6e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
KJBOBAIK_00252 | 1.6e-21 | |||||
KJBOBAIK_00253 | 3.8e-77 | comGF | U | Putative Competence protein ComGF | ||
KJBOBAIK_00254 | 2.3e-41 | |||||
KJBOBAIK_00255 | 1.8e-69 | |||||
KJBOBAIK_00256 | 3.9e-38 | comGC | U | competence protein ComGC | ||
KJBOBAIK_00257 | 4.1e-90 | comGB | NU | type II secretion system | ||
KJBOBAIK_00258 | 8.5e-83 | ybbH_2 | K | rpiR family | ||
KJBOBAIK_00259 | 3.4e-195 | S | Bacterial protein of unknown function (DUF871) | |||
KJBOBAIK_00260 | 6.5e-112 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
KJBOBAIK_00261 | 4.8e-86 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
KJBOBAIK_00262 | 1.8e-119 | S | Putative esterase | |||
KJBOBAIK_00263 | 4.8e-120 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
KJBOBAIK_00264 | 1.3e-79 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
KJBOBAIK_00265 | 8.5e-260 | qacA | EGP | Major facilitator Superfamily | ||
KJBOBAIK_00266 | 1.2e-171 | 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 | |
KJBOBAIK_00267 | 5.5e-75 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
KJBOBAIK_00271 | 7.5e-14 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
KJBOBAIK_00272 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
KJBOBAIK_00273 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
KJBOBAIK_00274 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
KJBOBAIK_00275 | 3.3e-80 | 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 | ||
KJBOBAIK_00276 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
KJBOBAIK_00277 | 1.3e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
KJBOBAIK_00278 | 4.3e-94 | |||||
KJBOBAIK_00280 | 7.3e-66 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
KJBOBAIK_00281 | 2e-149 | arcA | 3.5.3.6 | E | Arginine | |
KJBOBAIK_00282 | 2.9e-07 | 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 | ||
KJBOBAIK_00284 | 7.7e-86 | |||||
KJBOBAIK_00285 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
KJBOBAIK_00286 | 3.1e-136 | glcR | K | DeoR C terminal sensor domain | ||
KJBOBAIK_00287 | 2.5e-59 | S | Enterocin A Immunity | |||
KJBOBAIK_00288 | 1.2e-154 | S | hydrolase | |||
KJBOBAIK_00289 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
KJBOBAIK_00290 | 1e-70 | rplO | J | Binds to the 23S rRNA | ||
KJBOBAIK_00291 | 1.1e-237 | 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 | ||
KJBOBAIK_00292 | 3.5e-120 | 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 | |
KJBOBAIK_00293 | 8.4e-34 | 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 | ||
KJBOBAIK_00294 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
KJBOBAIK_00295 | 1.3e-43 | L | transposase, IS605 OrfB family | |||
KJBOBAIK_00296 | 2.1e-28 | S | Peptidase propeptide and YPEB domain | |||
KJBOBAIK_00297 | 2.4e-60 | ypaA | S | Protein of unknown function (DUF1304) | ||
KJBOBAIK_00298 | 2.3e-306 | oppA3 | E | ABC transporter, substratebinding protein | ||
KJBOBAIK_00299 | 9e-161 | V | ABC transporter transmembrane region | |||
KJBOBAIK_00300 | 8.6e-66 | V | ABC transporter transmembrane region | |||
KJBOBAIK_00301 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
KJBOBAIK_00302 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
KJBOBAIK_00303 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
KJBOBAIK_00304 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
KJBOBAIK_00305 | 1.4e-101 | T | GHKL domain | |||
KJBOBAIK_00306 | 2.8e-44 | K | FR47-like protein | |||
KJBOBAIK_00307 | 1.4e-25 | K | FR47-like protein | |||
KJBOBAIK_00308 | 1.6e-08 | |||||
KJBOBAIK_00310 | 2.5e-80 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
KJBOBAIK_00311 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
KJBOBAIK_00312 | 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 | |
KJBOBAIK_00313 | 2.3e-223 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
KJBOBAIK_00314 | 2.5e-89 | M | Protein of unknown function (DUF3737) | |||
KJBOBAIK_00316 | 1e-15 | S | Domain of Unknown Function with PDB structure (DUF3850) | |||
KJBOBAIK_00317 | 2.2e-165 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
KJBOBAIK_00318 | 2.6e-135 | fruR | K | DeoR C terminal sensor domain | ||
KJBOBAIK_00319 | 1.8e-218 | natB | CP | ABC-2 family transporter protein | ||
KJBOBAIK_00320 | 1e-19 | natA | S | ABC transporter, ATP-binding protein | ||
KJBOBAIK_00321 | 7.5e-52 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
KJBOBAIK_00322 | 1.6e-85 | |||||
KJBOBAIK_00323 | 3.6e-58 | |||||
KJBOBAIK_00324 | 4.1e-137 | hlyX | S | Transporter associated domain | ||
KJBOBAIK_00325 | 5.3e-37 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
KJBOBAIK_00326 | 2.9e-133 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
KJBOBAIK_00327 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
KJBOBAIK_00328 | 2e-258 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
KJBOBAIK_00329 | 1.4e-138 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
KJBOBAIK_00330 | 5.3e-150 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
KJBOBAIK_00331 | 2.1e-77 | 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) | |
KJBOBAIK_00332 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
KJBOBAIK_00333 | 8.8e-110 | yjbF | S | SNARE associated Golgi protein | ||
KJBOBAIK_00334 | 2.7e-151 | I | alpha/beta hydrolase fold | |||
KJBOBAIK_00335 | 5.2e-156 | hipB | K | Helix-turn-helix | ||
KJBOBAIK_00336 | 1.4e-15 | S | cog cog1373 | |||
KJBOBAIK_00337 | 1e-30 | S | cog cog1373 | |||
KJBOBAIK_00338 | 7.6e-91 | F | Nucleoside 2-deoxyribosyltransferase | |||
KJBOBAIK_00339 | 2.8e-157 | pstS | P | Phosphate | ||
KJBOBAIK_00340 | 3.6e-76 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
KJBOBAIK_00341 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
KJBOBAIK_00342 | 1.2e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
KJBOBAIK_00343 | 2.1e-282 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
KJBOBAIK_00344 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
KJBOBAIK_00346 | 3.3e-09 | arpU | S | Phage transcriptional regulator, ArpU family | ||
KJBOBAIK_00348 | 8.8e-23 | S | Alpha beta hydrolase | |||
KJBOBAIK_00349 | 1.2e-63 | S | Alpha beta hydrolase | |||
KJBOBAIK_00350 | 1.9e-37 | |||||
KJBOBAIK_00351 | 7e-50 | |||||
KJBOBAIK_00352 | 2.4e-147 | S | haloacid dehalogenase-like hydrolase | |||
KJBOBAIK_00353 | 1.8e-151 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KJBOBAIK_00354 | 1.3e-117 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KJBOBAIK_00355 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
KJBOBAIK_00356 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KJBOBAIK_00357 | 7.6e-49 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
KJBOBAIK_00358 | 3e-238 | cycA | E | Amino acid permease | ||
KJBOBAIK_00359 | 4.2e-84 | maa | S | transferase hexapeptide repeat | ||
KJBOBAIK_00360 | 3.3e-158 | K | Transcriptional regulator | |||
KJBOBAIK_00361 | 1.6e-61 | manO | S | Domain of unknown function (DUF956) | ||
KJBOBAIK_00362 | 2.1e-58 | manN | G | system, mannose fructose sorbose family IID component | ||
KJBOBAIK_00363 | 2.2e-112 | 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 | |||
KJBOBAIK_00364 | 2.7e-18 | M | Lysin motif | |||
KJBOBAIK_00365 | 7.2e-113 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
KJBOBAIK_00366 | 2.4e-23 | ecsB | U | ABC transporter | ||
KJBOBAIK_00367 | 1.6e-41 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KJBOBAIK_00368 | 3.6e-72 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
KJBOBAIK_00370 | 3.1e-21 | S | Protein of unknown function (DUF805) | |||
KJBOBAIK_00371 | 1.8e-53 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
KJBOBAIK_00372 | 2.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
KJBOBAIK_00373 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
KJBOBAIK_00374 | 1.3e-90 | 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 | ||
KJBOBAIK_00375 | 9.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
KJBOBAIK_00376 | 4.3e-40 | V | ABC transporter, ATP-binding protein | |||
KJBOBAIK_00377 | 0.0 | V | ABC transporter | |||
KJBOBAIK_00378 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
KJBOBAIK_00379 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
KJBOBAIK_00380 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
KJBOBAIK_00381 | 1.7e-100 | endA | F | DNA RNA non-specific endonuclease | ||
KJBOBAIK_00382 | 1.6e-266 | pipD | E | Dipeptidase | ||
KJBOBAIK_00383 | 1.9e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
KJBOBAIK_00384 | 1.6e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
KJBOBAIK_00385 | 1.1e-142 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
KJBOBAIK_00386 | 0.0 | kup | P | Transport of potassium into the cell | ||
KJBOBAIK_00387 | 1.4e-74 | 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 | |
KJBOBAIK_00388 | 3e-63 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
KJBOBAIK_00389 | 6.2e-91 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
KJBOBAIK_00390 | 1.7e-94 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
KJBOBAIK_00391 | 6.3e-35 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
KJBOBAIK_00392 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
KJBOBAIK_00393 | 4e-54 | 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 | ||
KJBOBAIK_00394 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
KJBOBAIK_00395 | 7.3e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
KJBOBAIK_00396 | 3.1e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
KJBOBAIK_00397 | 4.6e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
KJBOBAIK_00398 | 7.3e-107 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
KJBOBAIK_00399 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
KJBOBAIK_00400 | 8.5e-148 | 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 | ||
KJBOBAIK_00401 | 1.6e-100 | gntR1 | K | UTRA | ||
KJBOBAIK_00402 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
KJBOBAIK_00403 | 2.1e-134 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
KJBOBAIK_00404 | 8.3e-47 | arbx | M | Glycosyl transferase family 8 | ||
KJBOBAIK_00405 | 5e-184 | arbY | M | Glycosyl transferase family 8 | ||
KJBOBAIK_00406 | 9e-178 | arbY | M | Glycosyl transferase family 8 | ||
KJBOBAIK_00407 | 1.6e-151 | arbZ | I | Phosphate acyltransferases | ||
KJBOBAIK_00408 | 1.4e-36 | S | Cytochrome B5 | |||
KJBOBAIK_00409 | 9.5e-82 | XK27_04435 | 3.5.4.5 | J | FR47-like protein | |
KJBOBAIK_00410 | 2e-10 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
KJBOBAIK_00411 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
KJBOBAIK_00412 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
KJBOBAIK_00413 | 9.9e-124 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
KJBOBAIK_00414 | 1.7e-22 | blpT | ||||
KJBOBAIK_00415 | 4.6e-27 | S | Enterocin A Immunity | |||
KJBOBAIK_00418 | 1.3e-69 | doc | S | Prophage maintenance system killer protein | ||
KJBOBAIK_00419 | 2.9e-31 | |||||
KJBOBAIK_00420 | 0.0 | pepF | E | oligoendopeptidase F | ||
KJBOBAIK_00421 | 9.6e-196 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KJBOBAIK_00422 | 5.4e-63 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
KJBOBAIK_00423 | 5.7e-69 | rplI | J | Binds to the 23S rRNA | ||
KJBOBAIK_00424 | 6.7e-254 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
KJBOBAIK_00425 | 3.7e-100 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
KJBOBAIK_00426 | 2e-52 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
KJBOBAIK_00427 | 1.4e-167 | degV | S | DegV family | ||
KJBOBAIK_00428 | 2.5e-135 | V | ABC transporter transmembrane region | |||
KJBOBAIK_00429 | 6.7e-167 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
KJBOBAIK_00431 | 1.4e-16 | |||||
KJBOBAIK_00432 | 3.8e-193 | I | Protein of unknown function (DUF2974) | |||
KJBOBAIK_00433 | 2.5e-116 | yhiD | S | MgtC family | ||
KJBOBAIK_00435 | 7.6e-25 | S | SLAP domain | |||
KJBOBAIK_00436 | 4.3e-24 | S | SLAP domain | |||
KJBOBAIK_00437 | 5.7e-28 | |||||
KJBOBAIK_00440 | 4.9e-111 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_00441 | 2.5e-75 | K | Helix-turn-helix domain | |||
KJBOBAIK_00442 | 1.5e-25 | S | CAAX protease self-immunity | |||
KJBOBAIK_00443 | 1.4e-22 | S | CAAX protease self-immunity | |||
KJBOBAIK_00444 | 7.6e-26 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
KJBOBAIK_00446 | 3.5e-91 | ybaT | E | Amino acid permease | ||
KJBOBAIK_00447 | 1.7e-07 | S | LPXTG cell wall anchor motif | |||
KJBOBAIK_00448 | 2.6e-146 | S | Putative ABC-transporter type IV | |||
KJBOBAIK_00451 | 2e-113 | cbiQ | P | cobalt transport | ||
KJBOBAIK_00452 | 4.5e-143 | ykoD | P | ABC transporter, ATP-binding protein | ||
KJBOBAIK_00453 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
KJBOBAIK_00454 | 4.8e-148 | ylmH | S | S4 domain protein | ||
KJBOBAIK_00455 | 1.7e-45 | yggT | S | YGGT family | ||
KJBOBAIK_00456 | 7.3e-74 | 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 | ||
KJBOBAIK_00457 | 4.7e-15 | 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 | ||
KJBOBAIK_00458 | 2.4e-47 | 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 | ||
KJBOBAIK_00459 | 1.3e-134 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KJBOBAIK_00460 | 1.4e-40 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
KJBOBAIK_00461 | 7.9e-219 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
KJBOBAIK_00462 | 1.7e-142 | 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) | |
KJBOBAIK_00463 | 4.9e-85 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
KJBOBAIK_00464 | 1.4e-118 | D | Alpha beta | |||
KJBOBAIK_00471 | 8.1e-19 | |||||
KJBOBAIK_00475 | 8.9e-72 | ypuA | S | Protein of unknown function (DUF1002) | ||
KJBOBAIK_00477 | 7.2e-12 | L | Initiator Replication protein | |||
KJBOBAIK_00478 | 1.4e-28 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
KJBOBAIK_00479 | 1.2e-40 | L | AAA domain | |||
KJBOBAIK_00480 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KJBOBAIK_00481 | 2.9e-23 | |||||
KJBOBAIK_00482 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
KJBOBAIK_00483 | 1e-260 | |||||
KJBOBAIK_00484 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
KJBOBAIK_00485 | 4.7e-152 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
KJBOBAIK_00486 | 3.9e-25 | |||||
KJBOBAIK_00487 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
KJBOBAIK_00488 | 3.9e-24 | 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 | ||
KJBOBAIK_00489 | 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 | ||
KJBOBAIK_00490 | 1.2e-38 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KJBOBAIK_00491 | 1.4e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
KJBOBAIK_00492 | 9.6e-124 | skfE | V | ATPases associated with a variety of cellular activities | ||
KJBOBAIK_00493 | 7.2e-80 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KJBOBAIK_00494 | 2.8e-168 | K | LysR substrate binding domain | |||
KJBOBAIK_00495 | 2.3e-84 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
KJBOBAIK_00496 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
KJBOBAIK_00497 | 1.1e-228 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
KJBOBAIK_00498 | 1.1e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
KJBOBAIK_00499 | 5.2e-34 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
KJBOBAIK_00500 | 6.6e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
KJBOBAIK_00501 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
KJBOBAIK_00502 | 9.7e-59 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
KJBOBAIK_00503 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
KJBOBAIK_00504 | 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 | ||
KJBOBAIK_00505 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
KJBOBAIK_00506 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
KJBOBAIK_00507 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
KJBOBAIK_00508 | 7.7e-49 | 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 | |
KJBOBAIK_00509 | 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 | |
KJBOBAIK_00510 | 3.7e-121 | 3.6.3.8 | P | P-type ATPase | ||
KJBOBAIK_00511 | 1.1e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KJBOBAIK_00512 | 2.5e-52 | |||||
KJBOBAIK_00514 | 3.6e-13 | E | Pfam:DUF955 | |||
KJBOBAIK_00515 | 1.9e-21 | L | Psort location Cytoplasmic, score | |||
KJBOBAIK_00516 | 1.7e-23 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
KJBOBAIK_00517 | 9.6e-18 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
KJBOBAIK_00519 | 3.7e-133 | topA2 | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
KJBOBAIK_00521 | 3.8e-148 | camS | S | sex pheromone | ||
KJBOBAIK_00522 | 6.2e-48 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
KJBOBAIK_00523 | 2.5e-93 | 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) | |
KJBOBAIK_00524 | 1.3e-121 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
KJBOBAIK_00525 | 6.5e-146 | epsB | M | biosynthesis protein | ||
KJBOBAIK_00526 | 1.9e-176 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
KJBOBAIK_00529 | 6.4e-66 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
KJBOBAIK_00530 | 1e-93 | lacS | G | Transporter | ||
KJBOBAIK_00531 | 3.4e-36 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KJBOBAIK_00532 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KJBOBAIK_00538 | 3e-120 | |||||
KJBOBAIK_00539 | 9.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
KJBOBAIK_00540 | 1.1e-136 | S | Protein of unknown function (DUF3100) | |||
KJBOBAIK_00541 | 2.7e-246 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
KJBOBAIK_00542 | 5.4e-71 | Q | Imidazolonepropionase and related amidohydrolases | |||
KJBOBAIK_00543 | 3.9e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KJBOBAIK_00544 | 3.9e-229 | S | Tetratricopeptide repeat protein | |||
KJBOBAIK_00545 | 1e-93 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
KJBOBAIK_00546 | 4.4e-103 | K | Putative DNA-binding domain | |||
KJBOBAIK_00547 | 9.3e-35 | |||||
KJBOBAIK_00548 | 2.6e-70 | S | reductase | |||
KJBOBAIK_00552 | 1.6e-156 | ulaA | S | PTS system sugar-specific permease component | ||
KJBOBAIK_00553 | 1.5e-61 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
KJBOBAIK_00554 | 4.9e-80 | ulaG | S | Beta-lactamase superfamily domain | ||
KJBOBAIK_00555 | 6e-30 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
KJBOBAIK_00556 | 2.1e-123 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
KJBOBAIK_00557 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
KJBOBAIK_00558 | 3.8e-105 | vanZ | V | VanZ like family | ||
KJBOBAIK_00559 | 5.6e-130 | oppA | E | ABC transporter substrate-binding protein | ||
KJBOBAIK_00560 | 4.7e-91 | 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 | |
KJBOBAIK_00561 | 2e-49 | smc | D | Required for chromosome condensation and partitioning | ||
KJBOBAIK_00562 | 3.4e-08 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
KJBOBAIK_00563 | 2.5e-113 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
KJBOBAIK_00564 | 5.4e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
KJBOBAIK_00565 | 5.3e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
KJBOBAIK_00566 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
KJBOBAIK_00567 | 7.2e-181 | 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 | ||
KJBOBAIK_00568 | 1.9e-47 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
KJBOBAIK_00570 | 5.2e-130 | |||||
KJBOBAIK_00571 | 1.9e-25 | |||||
KJBOBAIK_00572 | 4.9e-181 | mco | Q | Multicopper oxidase | ||
KJBOBAIK_00573 | 5.5e-303 | V | FtsX-like permease family | |||
KJBOBAIK_00574 | 1.2e-97 | yfnA | E | amino acid | ||
KJBOBAIK_00575 | 3e-69 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
KJBOBAIK_00576 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
KJBOBAIK_00577 | 3.6e-24 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
KJBOBAIK_00578 | 1.6e-41 | |||||
KJBOBAIK_00579 | 2.1e-115 | M | NlpC/P60 family | |||
KJBOBAIK_00580 | 4e-59 | M | NlpC P60 family protein | |||
KJBOBAIK_00581 | 6e-51 | M | NlpC P60 family protein | |||
KJBOBAIK_00582 | 5e-88 | M | NlpC/P60 family | |||
KJBOBAIK_00583 | 2.2e-88 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
KJBOBAIK_00584 | 7.4e-23 | |||||
KJBOBAIK_00585 | 5.9e-134 | 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 | |
KJBOBAIK_00586 | 5e-154 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
KJBOBAIK_00587 | 2.5e-289 | S | membrane | |||
KJBOBAIK_00588 | 5.7e-169 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
KJBOBAIK_00589 | 1.3e-38 | S | RelB antitoxin | |||
KJBOBAIK_00590 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
KJBOBAIK_00591 | 6.7e-44 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KJBOBAIK_00592 | 6.1e-64 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
KJBOBAIK_00593 | 4.3e-68 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
KJBOBAIK_00594 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
KJBOBAIK_00595 | 8.5e-116 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
KJBOBAIK_00596 | 1.8e-142 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
KJBOBAIK_00600 | 2.6e-92 | S | UPF0397 protein | |||
KJBOBAIK_00601 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
KJBOBAIK_00602 | 1.5e-50 | |||||
KJBOBAIK_00603 | 2e-73 | citR | K | Putative sugar-binding domain | ||
KJBOBAIK_00604 | 4.9e-43 | M | Glycosyl hydrolases family 25 | |||
KJBOBAIK_00605 | 3.3e-39 | S | Phage capsid family | |||
KJBOBAIK_00606 | 5.5e-87 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
KJBOBAIK_00607 | 4.5e-134 | S | Phage portal protein | |||
KJBOBAIK_00609 | 1.1e-209 | S | Phage Terminase | |||
KJBOBAIK_00610 | 9e-47 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
KJBOBAIK_00611 | 3.4e-18 | N | HicA toxin of bacterial toxin-antitoxin, | |||
KJBOBAIK_00612 | 3.2e-56 | L | Phage terminase, small subunit | |||
KJBOBAIK_00613 | 1.2e-185 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
KJBOBAIK_00616 | 2.2e-27 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
KJBOBAIK_00617 | 2.4e-110 | K | WHG domain | |||
KJBOBAIK_00618 | 6.4e-96 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KJBOBAIK_00619 | 1.1e-27 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KJBOBAIK_00620 | 4.5e-168 | L | COG3385 FOG Transposase and inactivated derivatives | |||
KJBOBAIK_00621 | 1.6e-105 | tag | 3.2.2.20 | L | glycosylase | |
KJBOBAIK_00622 | 3.9e-84 | |||||
KJBOBAIK_00623 | 5.8e-28 | L | An automated process has identified a potential problem with this gene model | |||
KJBOBAIK_00624 | 3e-53 | cvpA | S | Colicin V production protein | ||
KJBOBAIK_00626 | 3.9e-142 | 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 | |
KJBOBAIK_00627 | 6e-151 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
KJBOBAIK_00628 | 1e-38 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
KJBOBAIK_00629 | 4.5e-226 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
KJBOBAIK_00630 | 1.2e-71 | scrR | K | Periplasmic binding protein domain | ||
KJBOBAIK_00631 | 7e-204 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
KJBOBAIK_00632 | 9.9e-280 | thrC | 4.2.3.1 | E | Threonine synthase | |
KJBOBAIK_00633 | 8.2e-48 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
KJBOBAIK_00634 | 3.3e-147 | glvR | K | Helix-turn-helix domain, rpiR family | ||
KJBOBAIK_00635 | 5.6e-78 | |||||
KJBOBAIK_00636 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
KJBOBAIK_00637 | 4.4e-37 | |||||
KJBOBAIK_00638 | 3.9e-119 | C | nitroreductase | |||
KJBOBAIK_00639 | 4.4e-242 | yhdP | S | Transporter associated domain | ||
KJBOBAIK_00640 | 3.7e-44 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KJBOBAIK_00641 | 9.8e-43 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
KJBOBAIK_00642 | 5.7e-186 | 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 | ||
KJBOBAIK_00643 | 1.5e-42 | 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 | ||
KJBOBAIK_00644 | 1.6e-43 | 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 | ||
KJBOBAIK_00645 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
KJBOBAIK_00646 | 9.2e-89 | ypmB | S | Protein conserved in bacteria | ||
KJBOBAIK_00647 | 3.4e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
KJBOBAIK_00648 | 2.2e-111 | dnaD | L | DnaD domain protein | ||
KJBOBAIK_00649 | 1.1e-42 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
KJBOBAIK_00650 | 1.5e-79 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
KJBOBAIK_00651 | 2e-45 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KJBOBAIK_00652 | 2.8e-29 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KJBOBAIK_00653 | 2.7e-263 | S | Fibronectin type III domain | |||
KJBOBAIK_00654 | 2.2e-43 | pbuX | F | xanthine permease | ||
KJBOBAIK_00655 | 2.5e-152 | msmR | K | AraC-like ligand binding domain | ||
KJBOBAIK_00656 | 2e-32 | dnaG | L | DNA primase activity | ||
KJBOBAIK_00658 | 2.7e-07 | |||||
KJBOBAIK_00660 | 1.9e-236 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
KJBOBAIK_00661 | 2.3e-284 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
KJBOBAIK_00662 | 1.2e-18 | S | D-Ala-teichoic acid biosynthesis protein | |||
KJBOBAIK_00663 | 4.1e-44 | |||||
KJBOBAIK_00664 | 1e-207 | ywhK | S | Membrane | ||
KJBOBAIK_00665 | 1.5e-80 | ykuL | S | (CBS) domain | ||
KJBOBAIK_00666 | 1.1e-56 | S | Protein of unknown function (DUF3290) | |||
KJBOBAIK_00667 | 3e-116 | yviA | S | Protein of unknown function (DUF421) | ||
KJBOBAIK_00668 | 3.7e-127 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
KJBOBAIK_00669 | 4.2e-176 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
KJBOBAIK_00670 | 9.3e-22 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
KJBOBAIK_00671 | 1.4e-107 | M | Transport protein ComB | |||
KJBOBAIK_00672 | 9.9e-135 | blpT | ||||
KJBOBAIK_00676 | 1.7e-31 | |||||
KJBOBAIK_00677 | 3e-21 | |||||
KJBOBAIK_00678 | 3.7e-83 | |||||
KJBOBAIK_00679 | 8.2e-31 | yozG | K | Transcriptional regulator | ||
KJBOBAIK_00680 | 3.4e-23 | |||||
KJBOBAIK_00681 | 1.7e-67 | |||||
KJBOBAIK_00682 | 5.9e-199 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
KJBOBAIK_00683 | 1.7e-66 | gmuR | K | UTRA | ||
KJBOBAIK_00686 | 3.9e-64 | |||||
KJBOBAIK_00687 | 5.1e-137 | |||||
KJBOBAIK_00688 | 2.1e-143 | |||||
KJBOBAIK_00689 | 1.4e-26 | |||||
KJBOBAIK_00690 | 1.9e-62 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
KJBOBAIK_00691 | 4.9e-142 | |||||
KJBOBAIK_00692 | 2.2e-168 | |||||
KJBOBAIK_00693 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
KJBOBAIK_00694 | 2.3e-245 | ynbB | 4.4.1.1 | P | aluminum resistance | |
KJBOBAIK_00695 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
KJBOBAIK_00696 | 2.3e-81 | xylG | 3.6.3.17 | S | ABC transporter | |
KJBOBAIK_00697 | 1.3e-197 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
KJBOBAIK_00698 | 3e-137 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
KJBOBAIK_00699 | 1.1e-68 | yeaE | S | Aldo/keto reductase family | ||
KJBOBAIK_00700 | 1.8e-77 | yeaE | S | Aldo/keto reductase family | ||
KJBOBAIK_00701 | 2.1e-134 | 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 | |
KJBOBAIK_00702 | 9.6e-119 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
KJBOBAIK_00703 | 9.3e-124 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
KJBOBAIK_00704 | 9.4e-72 | |||||
KJBOBAIK_00705 | 8.2e-140 | cof | S | haloacid dehalogenase-like hydrolase | ||
KJBOBAIK_00706 | 2.6e-308 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
KJBOBAIK_00707 | 7.7e-149 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
KJBOBAIK_00708 | 1.7e-34 | |||||
KJBOBAIK_00709 | 1.2e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
KJBOBAIK_00710 | 2e-106 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KJBOBAIK_00712 | 1.7e-132 | |||||
KJBOBAIK_00713 | 1.6e-143 | aatB | ET | ABC transporter substrate-binding protein | ||
KJBOBAIK_00714 | 2.5e-35 | yjcF | S | Acetyltransferase (GNAT) domain | ||
KJBOBAIK_00715 | 1.8e-20 | yjcF | S | Acetyltransferase (GNAT) domain | ||
KJBOBAIK_00716 | 7.1e-98 | E | GDSL-like Lipase/Acylhydrolase | |||
KJBOBAIK_00717 | 1e-165 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
KJBOBAIK_00718 | 1.6e-100 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
KJBOBAIK_00719 | 8.8e-58 | S | Peptidase propeptide and YPEB domain | |||
KJBOBAIK_00720 | 4.1e-19 | U | TraM recognition site of TraD and TraG | |||
KJBOBAIK_00724 | 3.8e-126 | |||||
KJBOBAIK_00725 | 4.4e-172 | S | Domain of unknown function (DUF389) | |||
KJBOBAIK_00726 | 6e-86 | |||||
KJBOBAIK_00727 | 5.7e-33 | K | LytTr DNA-binding domain | |||
KJBOBAIK_00728 | 5.9e-68 | S | Protein of unknown function (DUF3021) | |||
KJBOBAIK_00729 | 2.1e-139 | V | ABC transporter | |||
KJBOBAIK_00730 | 1.3e-102 | S | domain protein | |||
KJBOBAIK_00731 | 1.3e-229 | 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 | |
KJBOBAIK_00732 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
KJBOBAIK_00733 | 6.8e-110 | yjbK | S | CYTH | ||
KJBOBAIK_00734 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
KJBOBAIK_00735 | 3.8e-153 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
KJBOBAIK_00736 | 6.4e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KJBOBAIK_00737 | 2.4e-07 | S | Pfam:DUF955 | |||
KJBOBAIK_00738 | 8.8e-22 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_00739 | 1.4e-17 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_00740 | 3e-91 | S | DNA binding | |||
KJBOBAIK_00746 | 1.8e-31 | S | Helix-turn-helix domain | |||
KJBOBAIK_00747 | 5.5e-18 | |||||
KJBOBAIK_00749 | 4.6e-45 | |||||
KJBOBAIK_00750 | 9.4e-121 | S | Protein of unknown function (DUF1351) | |||
KJBOBAIK_00751 | 3.6e-112 | S | ERF superfamily | |||
KJBOBAIK_00752 | 1.2e-100 | L | Helix-turn-helix domain | |||
KJBOBAIK_00758 | 3.4e-17 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
KJBOBAIK_00761 | 1.3e-20 | lysM | M | LysM domain | ||
KJBOBAIK_00762 | 3.5e-166 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
KJBOBAIK_00763 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
KJBOBAIK_00764 | 2.7e-165 | pipD | E | Dipeptidase | ||
KJBOBAIK_00765 | 2e-74 | K | acetyltransferase | |||
KJBOBAIK_00766 | 9.6e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
KJBOBAIK_00767 | 6.7e-311 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
KJBOBAIK_00768 | 1.5e-46 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
KJBOBAIK_00769 | 1.1e-68 | S | Domain of unknown function (DUF1934) | |||
KJBOBAIK_00770 | 3.2e-269 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KJBOBAIK_00771 | 5.6e-43 | |||||
KJBOBAIK_00772 | 1.6e-171 | 2.7.1.2 | GK | ROK family | ||
KJBOBAIK_00773 | 9.9e-49 | 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 | |
KJBOBAIK_00774 | 1.7e-102 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
KJBOBAIK_00775 | 8.9e-295 | 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 | ||
KJBOBAIK_00777 | 1.2e-21 | 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 | ||
KJBOBAIK_00778 | 6.2e-99 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
KJBOBAIK_00779 | 2.8e-90 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
KJBOBAIK_00780 | 4.1e-31 | sgaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
KJBOBAIK_00781 | 7.1e-55 | ulaA | S | PTS system sugar-specific permease component | ||
KJBOBAIK_00782 | 1.1e-19 | camS | S | sex pheromone | ||
KJBOBAIK_00783 | 1e-229 | 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 | |
KJBOBAIK_00784 | 7.2e-82 | 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 | |
KJBOBAIK_00785 | 2.2e-20 | 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 | |
KJBOBAIK_00787 | 9e-126 | potC | P | ABC transporter permease | ||
KJBOBAIK_00788 | 7.3e-208 | potD | P | ABC transporter | ||
KJBOBAIK_00789 | 6.4e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
KJBOBAIK_00790 | 1e-159 | ybbR | S | YbbR-like protein | ||
KJBOBAIK_00791 | 9e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
KJBOBAIK_00792 | 3e-145 | S | hydrolase | |||
KJBOBAIK_00793 | 1.8e-75 | K | Penicillinase repressor | |||
KJBOBAIK_00794 | 1.6e-118 | |||||
KJBOBAIK_00795 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
KJBOBAIK_00796 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
KJBOBAIK_00797 | 8.3e-143 | licT | K | CAT RNA binding domain | ||
KJBOBAIK_00798 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
KJBOBAIK_00799 | 5.2e-10 | hicA | N | HicA toxin of bacterial toxin-antitoxin, | ||
KJBOBAIK_00800 | 2.7e-35 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
KJBOBAIK_00803 | 5.4e-206 | frdC | 1.3.5.4 | C | FAD binding domain | |
KJBOBAIK_00804 | 1.9e-40 | frdC | 1.3.5.4 | C | FAD binding domain | |
KJBOBAIK_00805 | 4.4e-152 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
KJBOBAIK_00806 | 8e-42 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
KJBOBAIK_00807 | 3.4e-21 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
KJBOBAIK_00808 | 1.1e-68 | metI | P | ABC transporter permease | ||
KJBOBAIK_00809 | 1.6e-183 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
KJBOBAIK_00810 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
KJBOBAIK_00811 | 1.3e-72 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
KJBOBAIK_00812 | 2.3e-213 | malE | G | Bacterial extracellular solute-binding protein | ||
KJBOBAIK_00813 | 3e-209 | msmX | P | Belongs to the ABC transporter superfamily | ||
KJBOBAIK_00814 | 5.4e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
KJBOBAIK_00815 | 4.6e-213 | S | SLAP domain | |||
KJBOBAIK_00816 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
KJBOBAIK_00817 | 3.5e-71 | yqeY | S | YqeY-like protein | ||
KJBOBAIK_00818 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
KJBOBAIK_00819 | 8.3e-151 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
KJBOBAIK_00820 | 1.5e-18 | S | CRISPR-associated protein (Cas_Csn2) | |||
KJBOBAIK_00821 | 1.9e-133 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
KJBOBAIK_00822 | 2.1e-168 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
KJBOBAIK_00823 | 2.2e-93 | 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 | |
KJBOBAIK_00824 | 3.1e-56 | phoH | T | phosphate starvation-inducible protein PhoH | ||
KJBOBAIK_00825 | 1.4e-245 | P | P-loop Domain of unknown function (DUF2791) | |||
KJBOBAIK_00826 | 2.6e-138 | S | TerB-C domain | |||
KJBOBAIK_00827 | 1.9e-94 | yjcE | P | Sodium proton antiporter | ||
KJBOBAIK_00828 | 1.5e-30 | yjcE | P | Sodium proton antiporter | ||
KJBOBAIK_00829 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
KJBOBAIK_00830 | 1.5e-107 | glnP | P | ABC transporter permease | ||
KJBOBAIK_00831 | 1.3e-102 | 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 | |
KJBOBAIK_00832 | 5e-17 | 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 | |
KJBOBAIK_00833 | 2.4e-19 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KJBOBAIK_00834 | 1.8e-34 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
KJBOBAIK_00835 | 1.2e-53 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
KJBOBAIK_00836 | 5.1e-251 | dnaB | L | Replication initiation and membrane attachment | ||
KJBOBAIK_00837 | 2.1e-168 | dnaI | L | Primosomal protein DnaI | ||
KJBOBAIK_00838 | 4.1e-244 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
KJBOBAIK_00839 | 1.6e-109 | 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 | |
KJBOBAIK_00840 | 5.7e-18 | |||||
KJBOBAIK_00841 | 3.3e-239 | G | Bacterial extracellular solute-binding protein | |||
KJBOBAIK_00842 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
KJBOBAIK_00843 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
KJBOBAIK_00845 | 0.0 | S | SLAP domain | |||
KJBOBAIK_00846 | 6.4e-86 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
KJBOBAIK_00847 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
KJBOBAIK_00848 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
KJBOBAIK_00849 | 3.4e-42 | S | RloB-like protein | |||
KJBOBAIK_00850 | 2e-254 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
KJBOBAIK_00851 | 1.6e-33 | rarA | L | MgsA AAA+ ATPase C terminal | ||
KJBOBAIK_00852 | 4.3e-226 | 2.7.1.207 | 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 | ||
KJBOBAIK_00855 | 5.1e-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 | |
KJBOBAIK_00856 | 8.8e-107 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KJBOBAIK_00857 | 2.2e-240 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
KJBOBAIK_00858 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
KJBOBAIK_00859 | 6.8e-60 | divIC | D | Septum formation initiator | ||
KJBOBAIK_00860 | 1.6e-33 | yabO | J | S4 domain protein | ||
KJBOBAIK_00861 | 6e-36 | 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 | ||
KJBOBAIK_00863 | 3.3e-77 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
KJBOBAIK_00864 | 1.7e-201 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
KJBOBAIK_00865 | 2.2e-120 | lsa | S | ABC transporter | ||
KJBOBAIK_00867 | 1e-205 | M | Glycosyl hydrolases family 25 | |||
KJBOBAIK_00868 | 1.7e-154 | cinI | S | Serine hydrolase (FSH1) | ||
KJBOBAIK_00869 | 7.9e-129 | S | Predicted membrane protein (DUF2207) | |||
KJBOBAIK_00870 | 5.2e-131 | yjeM | E | Amino Acid | ||
KJBOBAIK_00871 | 2.3e-192 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
KJBOBAIK_00872 | 1.7e-170 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
KJBOBAIK_00873 | 1.3e-18 | |||||
KJBOBAIK_00874 | 1.8e-78 | |||||
KJBOBAIK_00875 | 1.7e-139 | |||||
KJBOBAIK_00876 | 6.9e-100 | V | ATPases associated with a variety of cellular activities | |||
KJBOBAIK_00877 | 3.7e-146 | ykuT | M | mechanosensitive ion channel | ||
KJBOBAIK_00878 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
KJBOBAIK_00879 | 1.3e-36 | |||||
KJBOBAIK_00880 | 1.1e-203 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KJBOBAIK_00881 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
KJBOBAIK_00882 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
KJBOBAIK_00883 | 4.3e-55 | |||||
KJBOBAIK_00884 | 2.2e-33 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KJBOBAIK_00885 | 4.4e-162 | |||||
KJBOBAIK_00886 | 7.8e-26 | K | Acetyltransferase (GNAT) domain | |||
KJBOBAIK_00888 | 7.7e-127 | ydgH | S | MMPL family | ||
KJBOBAIK_00891 | 2.1e-146 | |||||
KJBOBAIK_00892 | 7.1e-185 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KJBOBAIK_00893 | 1.7e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KJBOBAIK_00894 | 1.4e-66 | 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 | |
KJBOBAIK_00896 | 5.3e-13 | I | mechanosensitive ion channel activity | |||
KJBOBAIK_00897 | 6.8e-86 | U | TraM recognition site of TraD and TraG | |||
KJBOBAIK_00898 | 3.2e-19 | |||||
KJBOBAIK_00902 | 1.4e-14 | |||||
KJBOBAIK_00903 | 4e-75 | S | Phage antirepressor protein KilAC domain | |||
KJBOBAIK_00904 | 6.5e-17 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_00905 | 9e-19 | K | Cro/C1-type HTH DNA-binding domain | |||
KJBOBAIK_00906 | 1.3e-19 | S | Pfam:Peptidase_M78 | |||
KJBOBAIK_00908 | 2.4e-135 | sip | L | Belongs to the 'phage' integrase family | ||
KJBOBAIK_00909 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
KJBOBAIK_00910 | 1.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
KJBOBAIK_00911 | 5.1e-142 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
KJBOBAIK_00912 | 2.7e-174 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
KJBOBAIK_00913 | 2.2e-292 | I | Acyltransferase | |||
KJBOBAIK_00914 | 1.4e-173 | 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 | ||
KJBOBAIK_00915 | 1.4e-173 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
KJBOBAIK_00916 | 7.3e-290 | S | SLAP domain | |||
KJBOBAIK_00917 | 5.3e-80 | |||||
KJBOBAIK_00918 | 2.6e-173 | 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 | |
KJBOBAIK_00919 | 1.5e-147 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
KJBOBAIK_00920 | 4.5e-39 | veg | S | Biofilm formation stimulator VEG | ||
KJBOBAIK_00921 | 6.7e-151 | 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 | |
KJBOBAIK_00922 | 1e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
KJBOBAIK_00923 | 1.3e-141 | yfeO | P | Voltage gated chloride channel | ||
KJBOBAIK_00924 | 6.4e-41 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
KJBOBAIK_00925 | 6e-126 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
KJBOBAIK_00926 | 1.4e-51 | |||||
KJBOBAIK_00927 | 2.1e-42 | |||||
KJBOBAIK_00928 | 2.3e-90 | EGP | Major facilitator Superfamily | |||
KJBOBAIK_00929 | 2.3e-69 | O | OsmC-like protein | |||
KJBOBAIK_00930 | 2.2e-85 | S | Protein of unknown function (DUF805) | |||
KJBOBAIK_00931 | 2.2e-78 | |||||
KJBOBAIK_00932 | 5.2e-93 | |||||
KJBOBAIK_00933 | 4.9e-179 | |||||
KJBOBAIK_00934 | 5.8e-83 | S | Fic/DOC family | |||
KJBOBAIK_00935 | 2.8e-33 | yjeM | E | Amino Acid | ||
KJBOBAIK_00936 | 1.5e-74 | yjeM | E | Amino Acid | ||
KJBOBAIK_00937 | 1.3e-111 | yjeM | E | Amino Acid | ||
KJBOBAIK_00938 | 1.4e-88 | 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 | |
KJBOBAIK_00939 | 2.3e-232 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
KJBOBAIK_00940 | 4.2e-30 | K | Helix-turn-helix | |||
KJBOBAIK_00941 | 5e-57 | 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 | |
KJBOBAIK_00942 | 3.1e-113 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
KJBOBAIK_00943 | 3.6e-174 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
KJBOBAIK_00944 | 5.1e-176 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
KJBOBAIK_00945 | 1.4e-81 | L | COG3385 FOG Transposase and inactivated derivatives | |||
KJBOBAIK_00946 | 1.3e-148 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
KJBOBAIK_00947 | 5.1e-118 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
KJBOBAIK_00948 | 3e-139 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
KJBOBAIK_00949 | 1.2e-161 | phnD | P | Phosphonate ABC transporter | ||
KJBOBAIK_00951 | 2.2e-82 | uspA | T | universal stress protein | ||
KJBOBAIK_00952 | 3.7e-183 | L | Phage integrase family | |||
KJBOBAIK_00953 | 4.8e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
KJBOBAIK_00954 | 5.9e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
KJBOBAIK_00955 | 8.4e-145 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
KJBOBAIK_00956 | 1.6e-135 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
KJBOBAIK_00957 | 4.6e-157 | ecfA | 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 | |
KJBOBAIK_00958 | 8.2e-154 | 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 | ||
KJBOBAIK_00959 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
KJBOBAIK_00960 | 5.8e-169 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
KJBOBAIK_00961 | 7.9e-92 | liaI | S | membrane | ||
KJBOBAIK_00962 | 4e-16 | |||||
KJBOBAIK_00963 | 3.9e-186 | S | Putative peptidoglycan binding domain | |||
KJBOBAIK_00964 | 1.9e-157 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
KJBOBAIK_00965 | 4.2e-118 | |||||
KJBOBAIK_00967 | 3.8e-15 | |||||
KJBOBAIK_00968 | 1.8e-159 | trsE | S | COG0433 Predicted ATPase | ||
KJBOBAIK_00969 | 2.9e-58 | S | Protein of unknown function (DUF554) | |||
KJBOBAIK_00970 | 1.2e-30 | |||||
KJBOBAIK_00971 | 1.4e-34 | |||||
KJBOBAIK_00972 | 3.3e-54 | rimL | J | Acetyltransferase (GNAT) domain | ||
KJBOBAIK_00974 | 8.3e-58 | |||||
KJBOBAIK_00975 | 4.9e-61 | S | ABC transporter | |||
KJBOBAIK_00976 | 1.1e-186 | S | ABC transporter | |||
KJBOBAIK_00977 | 3.9e-66 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
KJBOBAIK_00978 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
KJBOBAIK_00979 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
KJBOBAIK_00980 | 5.3e-26 | |||||
KJBOBAIK_00981 | 2e-109 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
KJBOBAIK_00982 | 2e-52 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
KJBOBAIK_00983 | 2.1e-149 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
KJBOBAIK_00985 | 7.9e-269 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
KJBOBAIK_00986 | 5.5e-36 | |||||
KJBOBAIK_00987 | 1.7e-160 | scrR | K | Periplasmic binding protein domain | ||
KJBOBAIK_00988 | 4.6e-45 | 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 | ||
KJBOBAIK_00989 | 1.6e-111 | M | Peptidase family M1 domain | |||
KJBOBAIK_00990 | 6.3e-46 | S | SLAP domain | |||
KJBOBAIK_00991 | 2.6e-106 | S | SLAP domain | |||
KJBOBAIK_00992 | 3.8e-208 | mepA | V | MATE efflux family protein | ||
KJBOBAIK_00993 | 5.2e-90 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
KJBOBAIK_00994 | 3.9e-290 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
KJBOBAIK_00995 | 1.3e-153 | pipD | E | Dipeptidase | ||
KJBOBAIK_00997 | 6.3e-14 | |||||
KJBOBAIK_00998 | 8.5e-131 | cysA | V | ABC transporter, ATP-binding protein | ||
KJBOBAIK_00999 | 9.9e-97 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
KJBOBAIK_01000 | 1.6e-171 | K | Transcriptional regulator | |||
KJBOBAIK_01001 | 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 | |
KJBOBAIK_01002 | 3.5e-203 | 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 | |
KJBOBAIK_01003 | 2.8e-100 | S | ECF transporter, substrate-specific component | |||
KJBOBAIK_01004 | 3.9e-81 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
KJBOBAIK_01005 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
KJBOBAIK_01006 | 9.7e-97 | M | ErfK YbiS YcfS YnhG | |||
KJBOBAIK_01007 | 2e-152 | 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 | |
KJBOBAIK_01008 | 6.7e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
KJBOBAIK_01010 | 4.7e-46 | pspC | KT | PspC domain | ||
KJBOBAIK_01011 | 3.3e-237 | L | COG2963 Transposase and inactivated derivatives | |||
KJBOBAIK_01013 | 6e-115 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
KJBOBAIK_01014 | 7.7e-115 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
KJBOBAIK_01015 | 1.2e-100 | G | Histidine phosphatase superfamily (branch 1) | |||
KJBOBAIK_01016 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
KJBOBAIK_01017 | 2.4e-158 | D | nuclear chromosome segregation | |||
KJBOBAIK_01018 | 0.0 | typA | T | GTP-binding protein TypA | ||
KJBOBAIK_01019 | 8.9e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
KJBOBAIK_01020 | 1.3e-21 | |||||
KJBOBAIK_01021 | 3.5e-32 | ykzG | S | Belongs to the UPF0356 family | ||
KJBOBAIK_01022 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
KJBOBAIK_01023 | 1.7e-10 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
KJBOBAIK_01024 | 2.9e-35 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |||
KJBOBAIK_01025 | 9.4e-40 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
KJBOBAIK_01026 | 8.5e-21 | |||||
KJBOBAIK_01027 | 2.7e-63 | L | PFAM IS66 Orf2 family protein | |||
KJBOBAIK_01028 | 8.7e-34 | S | Transposase C of IS166 homeodomain | |||
KJBOBAIK_01029 | 4.1e-245 | L | Transposase IS66 family | |||
KJBOBAIK_01031 | 5.6e-179 | S | PFAM Archaeal ATPase | |||
KJBOBAIK_01032 | 2.4e-73 | S | cog cog1373 | |||
KJBOBAIK_01033 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
KJBOBAIK_01034 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
KJBOBAIK_01036 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
KJBOBAIK_01037 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
KJBOBAIK_01038 | 1e-193 | S | DUF218 domain | |||
KJBOBAIK_01039 | 2.7e-120 | S | CAAX protease self-immunity | |||
KJBOBAIK_01040 | 3e-111 | ropB | K | Transcriptional regulator | ||
KJBOBAIK_01041 | 4.2e-154 | EGP | Major facilitator Superfamily | |||
KJBOBAIK_01042 | 5.4e-51 | |||||
KJBOBAIK_01043 | 2.6e-155 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
KJBOBAIK_01044 | 9.8e-270 | V | ABC transporter transmembrane region | |||
KJBOBAIK_01045 | 2.3e-41 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
KJBOBAIK_01046 | 1.9e-47 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
KJBOBAIK_01047 | 5.3e-204 | napA | P | Sodium/hydrogen exchanger family | ||
KJBOBAIK_01048 | 9.4e-53 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KJBOBAIK_01049 | 8.4e-201 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
KJBOBAIK_01050 | 7.7e-76 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
KJBOBAIK_01051 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
KJBOBAIK_01052 | 1.5e-201 | pbpX1 | V | Beta-lactamase | ||
KJBOBAIK_01055 | 1.8e-07 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_01056 | 8e-09 | |||||
KJBOBAIK_01059 | 4.3e-98 | S | AntA/AntB antirepressor | |||
KJBOBAIK_01060 | 2.9e-12 | |||||
KJBOBAIK_01065 | 7.4e-25 | K | BRO family, N-terminal domain | |||
KJBOBAIK_01066 | 4.9e-08 | |||||
KJBOBAIK_01071 | 7.1e-38 | |||||
KJBOBAIK_01072 | 1.1e-18 | S | Phage uncharacterised protein (Phage_XkdX) | |||
KJBOBAIK_01075 | 3e-18 | |||||
KJBOBAIK_01076 | 5e-29 | |||||
KJBOBAIK_01077 | 1.4e-200 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
KJBOBAIK_01078 | 3.8e-88 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
KJBOBAIK_01079 | 5.1e-63 | S | Phage portal protein | |||
KJBOBAIK_01080 | 1.1e-141 | 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 | |
KJBOBAIK_01081 | 2.3e-133 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
KJBOBAIK_01082 | 1.7e-160 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
KJBOBAIK_01083 | 4.1e-176 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
KJBOBAIK_01084 | 4.1e-242 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
KJBOBAIK_01087 | 1.7e-12 | |||||
KJBOBAIK_01094 | 1.3e-54 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
KJBOBAIK_01095 | 4.7e-25 | S | Protein conserved in bacteria | |||
KJBOBAIK_01096 | 3.9e-57 | |||||
KJBOBAIK_01097 | 4.7e-85 | |||||
KJBOBAIK_01098 | 9.3e-264 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
KJBOBAIK_01099 | 5.8e-186 | XK27_05540 | S | DUF218 domain | ||
KJBOBAIK_01100 | 6.6e-108 | |||||
KJBOBAIK_01102 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
KJBOBAIK_01103 | 5.8e-45 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
KJBOBAIK_01104 | 4.8e-58 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
KJBOBAIK_01105 | 2.2e-70 | epsU | S | Polysaccharide biosynthesis protein | ||
KJBOBAIK_01106 | 9.1e-173 | epsU | S | Polysaccharide biosynthesis protein | ||
KJBOBAIK_01107 | 1.9e-106 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
KJBOBAIK_01108 | 0.0 | S | SH3-like domain | |||
KJBOBAIK_01109 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
KJBOBAIK_01110 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
KJBOBAIK_01111 | 1.4e-129 | 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 | ||
KJBOBAIK_01112 | 3.5e-199 | 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 | ||
KJBOBAIK_01113 | 4.7e-252 | 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 | ||
KJBOBAIK_01114 | 3.2e-145 | 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 | ||
KJBOBAIK_01115 | 3.5e-61 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
KJBOBAIK_01116 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
KJBOBAIK_01117 | 1.4e-34 | |||||
KJBOBAIK_01118 | 2.4e-62 | |||||
KJBOBAIK_01121 | 5.2e-118 | |||||
KJBOBAIK_01122 | 3.8e-104 | pncA | Q | Isochorismatase family | ||
KJBOBAIK_01124 | 2e-35 | |||||
KJBOBAIK_01125 | 5.8e-15 | |||||
KJBOBAIK_01126 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
KJBOBAIK_01127 | 3.5e-109 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
KJBOBAIK_01128 | 2.5e-141 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KJBOBAIK_01129 | 2.3e-235 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
KJBOBAIK_01130 | 1.8e-54 | ftsL | D | Cell division protein FtsL | ||
KJBOBAIK_01131 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
KJBOBAIK_01132 | 2.1e-73 | mraZ | K | Belongs to the MraZ family | ||
KJBOBAIK_01133 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
KJBOBAIK_01135 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
KJBOBAIK_01136 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
KJBOBAIK_01137 | 6.6e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
KJBOBAIK_01138 | 1.7e-144 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
KJBOBAIK_01139 | 1.8e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
KJBOBAIK_01140 | 2.3e-240 | G | Bacterial extracellular solute-binding protein | |||
KJBOBAIK_01141 | 4.6e-196 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
KJBOBAIK_01142 | 1.9e-75 | M | LysM domain | |||
KJBOBAIK_01143 | 1.3e-42 | |||||
KJBOBAIK_01144 | 2.5e-80 | 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) | |
KJBOBAIK_01145 | 3.4e-53 | |||||
KJBOBAIK_01147 | 7.1e-250 | pepC | 3.4.22.40 | E | aminopeptidase | |
KJBOBAIK_01148 | 1.3e-122 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
KJBOBAIK_01149 | 5e-301 | oppA | E | ABC transporter, substratebinding protein | ||
KJBOBAIK_01150 | 3.6e-88 | oppA | E | ABC transporter, substratebinding protein | ||
KJBOBAIK_01155 | 1.4e-304 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
KJBOBAIK_01156 | 1.5e-79 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
KJBOBAIK_01159 | 1.4e-256 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
KJBOBAIK_01160 | 1.3e-107 | tdk | 2.7.1.21 | F | thymidine kinase | |
KJBOBAIK_01161 | 1.3e-42 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KJBOBAIK_01162 | 2.3e-122 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
KJBOBAIK_01163 | 3.1e-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 | |
KJBOBAIK_01164 | 2.9e-41 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
KJBOBAIK_01165 | 2.1e-79 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
KJBOBAIK_01166 | 1e-218 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
KJBOBAIK_01167 | 3.2e-28 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
KJBOBAIK_01168 | 2.3e-78 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
KJBOBAIK_01169 | 2.1e-32 | |||||
KJBOBAIK_01170 | 3.7e-59 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
KJBOBAIK_01171 | 1e-151 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_01172 | 3.9e-298 | V | ABC transporter transmembrane region | |||
KJBOBAIK_01173 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
KJBOBAIK_01174 | 1.3e-96 | S | TerB-C domain | |||
KJBOBAIK_01175 | 6.7e-72 | S | TerB-C domain | |||
KJBOBAIK_01177 | 1.6e-45 | S | PFAM Archaeal ATPase | |||
KJBOBAIK_01178 | 7.3e-74 | |||||
KJBOBAIK_01179 | 2.6e-43 | kup | P | Transport of potassium into the cell | ||
KJBOBAIK_01180 | 3.7e-77 | M | LysM domain protein | |||
KJBOBAIK_01181 | 2.8e-86 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KJBOBAIK_01182 | 4.1e-78 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KJBOBAIK_01183 | 1.5e-16 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KJBOBAIK_01184 | 6.2e-12 | |||||
KJBOBAIK_01185 | 8.9e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
KJBOBAIK_01186 | 2.3e-30 | |||||
KJBOBAIK_01188 | 2.9e-69 | S | Iron-sulphur cluster biosynthesis | |||
KJBOBAIK_01189 | 6.5e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
KJBOBAIK_01190 | 6.2e-59 | psiE | S | Phosphate-starvation-inducible E | ||
KJBOBAIK_01192 | 2.2e-134 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
KJBOBAIK_01193 | 4.3e-228 | amtB | P | ammonium transporter | ||
KJBOBAIK_01194 | 1.4e-60 | |||||
KJBOBAIK_01195 | 4.5e-202 | lhr | L | DEAD DEAH box helicase | ||
KJBOBAIK_01196 | 8.4e-99 | 3.6.1.55 | F | NUDIX domain | ||
KJBOBAIK_01197 | 8.2e-75 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
KJBOBAIK_01198 | 5.6e-104 | glvR | K | Helix-turn-helix domain, rpiR family | ||
KJBOBAIK_01199 | 2.3e-184 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
KJBOBAIK_01200 | 5.9e-09 | |||||
KJBOBAIK_01201 | 4.4e-43 | |||||
KJBOBAIK_01202 | 6.9e-181 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
KJBOBAIK_01203 | 2.8e-51 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
KJBOBAIK_01204 | 2e-37 | clcA | P | chloride | ||
KJBOBAIK_01205 | 1.6e-60 | clcA | P | chloride | ||
KJBOBAIK_01206 | 4.7e-26 | K | FCD | |||
KJBOBAIK_01207 | 1.3e-221 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
KJBOBAIK_01208 | 2e-61 | 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 | ||
KJBOBAIK_01209 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
KJBOBAIK_01210 | 2.6e-103 | pbpX | V | Beta-lactamase | ||
KJBOBAIK_01211 | 5.7e-101 | nhaC | C | Na H antiporter NhaC | ||
KJBOBAIK_01212 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
KJBOBAIK_01213 | 3.4e-163 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KJBOBAIK_01214 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
KJBOBAIK_01215 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
KJBOBAIK_01216 | 1.5e-95 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
KJBOBAIK_01217 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KJBOBAIK_01218 | 2.2e-192 | 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 | |
KJBOBAIK_01219 | 1.3e-79 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
KJBOBAIK_01220 | 5.5e-77 | nrdI | F | NrdI Flavodoxin like | ||
KJBOBAIK_01221 | 9.9e-177 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
KJBOBAIK_01222 | 8.6e-69 | |||||
KJBOBAIK_01223 | 2.7e-134 | yvpB | S | Peptidase_C39 like family | ||
KJBOBAIK_01224 | 1.1e-83 | S | Threonine/Serine exporter, ThrE | |||
KJBOBAIK_01225 | 1.2e-86 | thrE | S | Putative threonine/serine exporter | ||
KJBOBAIK_01226 | 7.5e-28 | E | GDSL-like Lipase/Acylhydrolase family | |||
KJBOBAIK_01227 | 2.4e-110 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
KJBOBAIK_01228 | 3e-38 | ynzC | S | UPF0291 protein | ||
KJBOBAIK_01229 | 5.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
KJBOBAIK_01230 | 6.9e-284 | mdlA | V | ABC transporter | ||
KJBOBAIK_01231 | 5.8e-25 | mdlA | V | ABC transporter | ||
KJBOBAIK_01232 | 0.0 | mdlB | V | ABC transporter | ||
KJBOBAIK_01233 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
KJBOBAIK_01234 | 2.9e-41 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
KJBOBAIK_01235 | 6.7e-105 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
KJBOBAIK_01236 | 2.9e-116 | plsC | 2.3.1.51 | I | Acyltransferase | |
KJBOBAIK_01237 | 3e-195 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
KJBOBAIK_01238 | 1.8e-75 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KJBOBAIK_01239 | 8.9e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
KJBOBAIK_01240 | 1.5e-155 | holB | 2.7.7.7 | L | DNA polymerase III | |
KJBOBAIK_01241 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
KJBOBAIK_01242 | 2.3e-07 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KJBOBAIK_01243 | 6.2e-288 | P | ABC transporter | |||
KJBOBAIK_01244 | 4.3e-36 | |||||
KJBOBAIK_01246 | 6.8e-124 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
KJBOBAIK_01247 | 2.5e-86 | K | GNAT family | |||
KJBOBAIK_01248 | 2.7e-202 | XK27_00915 | C | Luciferase-like monooxygenase | ||
KJBOBAIK_01249 | 2.9e-122 | rbtT | P | Major Facilitator Superfamily | ||
KJBOBAIK_01250 | 1.1e-138 | stp | 3.1.3.16 | T | phosphatase | |
KJBOBAIK_01251 | 6.5e-99 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
KJBOBAIK_01252 | 2.2e-209 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
KJBOBAIK_01253 | 2.4e-127 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
KJBOBAIK_01254 | 1.9e-211 | pepC | 3.4.22.40 | E | aminopeptidase | |
KJBOBAIK_01255 | 2.3e-173 | oppF | P | Belongs to the ABC transporter superfamily | ||
KJBOBAIK_01256 | 7.7e-194 | oppD | P | Belongs to the ABC transporter superfamily | ||
KJBOBAIK_01257 | 8.9e-187 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KJBOBAIK_01258 | 6.8e-44 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
KJBOBAIK_01259 | 8.3e-24 | papP | P | ABC transporter, permease protein | ||
KJBOBAIK_01261 | 4.5e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
KJBOBAIK_01262 | 6.8e-81 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
KJBOBAIK_01263 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
KJBOBAIK_01264 | 1.4e-75 | UW | LPXTG-motif cell wall anchor domain protein | |||
KJBOBAIK_01265 | 3.2e-68 | UW | LPXTG-motif cell wall anchor domain protein | |||
KJBOBAIK_01266 | 4.4e-130 | UW | LPXTG-motif cell wall anchor domain protein | |||
KJBOBAIK_01267 | 8e-141 | L | An automated process has identified a potential problem with this gene model | |||
KJBOBAIK_01268 | 3.3e-179 | |||||
KJBOBAIK_01269 | 4.4e-42 | oppA2 | E | ABC transporter, substratebinding protein | ||
KJBOBAIK_01270 | 5.9e-236 | oppA2 | E | ABC transporter, substratebinding protein | ||
KJBOBAIK_01273 | 1.5e-237 | npr | 1.11.1.1 | C | NADH oxidase | |
KJBOBAIK_01274 | 6.6e-11 | |||||
KJBOBAIK_01275 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
KJBOBAIK_01276 | 6.7e-228 | slpX | S | SLAP domain | ||
KJBOBAIK_01277 | 2.4e-44 | K | SIS domain | |||
KJBOBAIK_01278 | 1.1e-53 | K | SIS domain | |||
KJBOBAIK_01279 | 2.9e-277 | V | ABC transporter transmembrane region | |||
KJBOBAIK_01280 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
KJBOBAIK_01281 | 5.7e-86 | T | Transcriptional regulatory protein, C terminal | |||
KJBOBAIK_01285 | 1.1e-209 | 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 | ||
KJBOBAIK_01286 | 1.3e-57 | 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 | ||
KJBOBAIK_01287 | 3.4e-13 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
KJBOBAIK_01288 | 1.5e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
KJBOBAIK_01289 | 7.6e-177 | pbpX2 | V | Beta-lactamase | ||
KJBOBAIK_01290 | 2.3e-133 | S | Protein of unknown function (DUF975) | |||
KJBOBAIK_01291 | 2.5e-116 | lysA2 | M | Glycosyl hydrolases family 25 | ||
KJBOBAIK_01292 | 7.9e-291 | ytgP | S | Polysaccharide biosynthesis protein | ||
KJBOBAIK_01293 | 1.9e-36 | |||||
KJBOBAIK_01294 | 3e-246 | XK27_06780 | V | ABC transporter permease | ||
KJBOBAIK_01295 | 1.3e-273 | E | amino acid | |||
KJBOBAIK_01296 | 0.0 | L | Helicase C-terminal domain protein | |||
KJBOBAIK_01297 | 4.8e-205 | pbpX1 | V | Beta-lactamase | ||
KJBOBAIK_01298 | 1.5e-225 | N | Uncharacterized conserved protein (DUF2075) | |||
KJBOBAIK_01299 | 5.8e-13 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
KJBOBAIK_01300 | 2.4e-43 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
KJBOBAIK_01302 | 4.9e-246 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KJBOBAIK_01303 | 5.4e-71 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
KJBOBAIK_01304 | 8.7e-60 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
KJBOBAIK_01305 | 1.7e-54 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
KJBOBAIK_01306 | 6.4e-128 | K | UTRA domain | |||
KJBOBAIK_01307 | 4e-72 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
KJBOBAIK_01308 | 7.9e-94 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
KJBOBAIK_01309 | 1.4e-178 | comGA | NU | Type II IV secretion system protein | ||
KJBOBAIK_01310 | 1.9e-130 | yebC | K | Transcriptional regulatory protein | ||
KJBOBAIK_01311 | 1.5e-203 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
KJBOBAIK_01312 | 5.7e-302 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
KJBOBAIK_01313 | 8e-145 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
KJBOBAIK_01314 | 1.4e-53 | S | Enterocin A Immunity | |||
KJBOBAIK_01315 | 2.5e-33 | |||||
KJBOBAIK_01316 | 9.5e-26 | |||||
KJBOBAIK_01317 | 1e-24 | |||||
KJBOBAIK_01318 | 3e-270 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
KJBOBAIK_01319 | 1.3e-91 | S | ECF-type riboflavin transporter, S component | |||
KJBOBAIK_01320 | 1.3e-229 | S | Putative peptidoglycan binding domain | |||
KJBOBAIK_01321 | 9e-83 | K | Acetyltransferase (GNAT) domain | |||
KJBOBAIK_01322 | 1.1e-250 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
KJBOBAIK_01323 | 9.5e-191 | yrvN | L | AAA C-terminal domain | ||
KJBOBAIK_01324 | 8.2e-64 | spxA_2 | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
KJBOBAIK_01325 | 7e-167 | treB | G | phosphotransferase system | ||
KJBOBAIK_01326 | 1.1e-164 | 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 | ||
KJBOBAIK_01327 | 1.2e-45 | E | Amino acid permease | |||
KJBOBAIK_01328 | 6.3e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
KJBOBAIK_01329 | 1.4e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
KJBOBAIK_01330 | 2.5e-176 | 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 | |
KJBOBAIK_01331 | 1.2e-77 | 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 | ||
KJBOBAIK_01332 | 3.2e-156 | 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 | ||
KJBOBAIK_01333 | 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) | |
KJBOBAIK_01334 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
KJBOBAIK_01335 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
KJBOBAIK_01336 | 6.7e-37 | |||||
KJBOBAIK_01337 | 3.4e-135 | glnQ | E | ABC transporter, ATP-binding protein | ||
KJBOBAIK_01338 | 1.1e-289 | glnP | P | ABC transporter permease | ||
KJBOBAIK_01339 | 4.9e-119 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
KJBOBAIK_01340 | 5.8e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
KJBOBAIK_01341 | 1.3e-124 | terC | P | Integral membrane protein TerC family | ||
KJBOBAIK_01342 | 9.2e-92 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
KJBOBAIK_01343 | 8.5e-133 | cobB | K | SIR2 family | ||
KJBOBAIK_01344 | 1.7e-136 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
KJBOBAIK_01345 | 7.1e-262 | V | ABC-type multidrug transport system, ATPase and permease components | |||
KJBOBAIK_01346 | 7.7e-195 | U | TraM recognition site of TraD and TraG | |||
KJBOBAIK_01347 | 1.1e-28 | 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 | |
KJBOBAIK_01349 | 2.5e-37 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
KJBOBAIK_01350 | 4.3e-127 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
KJBOBAIK_01351 | 5.4e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
KJBOBAIK_01352 | 5.4e-148 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KJBOBAIK_01353 | 1.1e-107 | fhuC | P | ABC transporter | ||
KJBOBAIK_01354 | 1.2e-180 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
KJBOBAIK_01355 | 3.2e-147 | yxeH | S | hydrolase | ||
KJBOBAIK_01356 | 2.7e-32 | S | reductase | |||
KJBOBAIK_01357 | 4.4e-39 | S | reductase | |||
KJBOBAIK_01358 | 2.4e-33 | S | reductase | |||
KJBOBAIK_01359 | 2.6e-92 | 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 | |
KJBOBAIK_01360 | 9.5e-31 | |||||
KJBOBAIK_01361 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
KJBOBAIK_01362 | 8e-162 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
KJBOBAIK_01363 | 6.1e-143 | V | Pfam:Methyltransf_26 | |||
KJBOBAIK_01364 | 5.2e-40 | V | Type II restriction enzyme, methylase subunits | |||
KJBOBAIK_01367 | 3.5e-205 | 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 | |
KJBOBAIK_01368 | 1.4e-25 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KJBOBAIK_01369 | 9.5e-183 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
KJBOBAIK_01370 | 1.6e-41 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
KJBOBAIK_01371 | 1.1e-150 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
KJBOBAIK_01372 | 1.4e-204 | tnpB | L | Putative transposase DNA-binding domain | ||
KJBOBAIK_01373 | 8.1e-62 | pacL | 3.6.3.8 | P | P-type ATPase | |
KJBOBAIK_01374 | 5.4e-76 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
KJBOBAIK_01375 | 2.9e-187 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
KJBOBAIK_01376 | 6.4e-162 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
KJBOBAIK_01377 | 2e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
KJBOBAIK_01378 | 2.4e-38 | K | Periplasmic binding protein-like domain | |||
KJBOBAIK_01379 | 1.6e-294 | L | Nuclease-related domain | |||
KJBOBAIK_01380 | 1.5e-73 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
KJBOBAIK_01381 | 5.5e-84 | S | PFAM Archaeal ATPase | |||
KJBOBAIK_01382 | 5.7e-84 | S | PFAM Archaeal ATPase | |||
KJBOBAIK_01383 | 7.7e-26 | |||||
KJBOBAIK_01384 | 3.1e-71 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
KJBOBAIK_01387 | 6.2e-165 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
KJBOBAIK_01389 | 2.7e-55 | 3.6.1.27 | I | Acid phosphatase homologues | ||
KJBOBAIK_01390 | 6.1e-102 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
KJBOBAIK_01391 | 5e-72 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
KJBOBAIK_01392 | 3.2e-192 | uvrA3 | L | excinuclease ABC, A subunit | ||
KJBOBAIK_01393 | 3.4e-123 | 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 | ||
KJBOBAIK_01394 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
KJBOBAIK_01395 | 6e-291 | clpE | O | Belongs to the ClpA ClpB family | ||
KJBOBAIK_01396 | 5.3e-103 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KJBOBAIK_01397 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
KJBOBAIK_01398 | 1.6e-70 | S | PAS domain | |||
KJBOBAIK_01399 | 9.1e-204 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
KJBOBAIK_01400 | 2e-177 | yvdE | K | helix_turn _helix lactose operon repressor | ||
KJBOBAIK_01401 | 7e-144 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
KJBOBAIK_01402 | 2.2e-193 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
KJBOBAIK_01403 | 7.7e-242 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
KJBOBAIK_01404 | 1.2e-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 | |
KJBOBAIK_01408 | 7.2e-189 | oppA | E | ABC transporter, substratebinding protein | ||
KJBOBAIK_01409 | 3.1e-209 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
KJBOBAIK_01410 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein | |||
KJBOBAIK_01414 | 3e-72 | |||||
KJBOBAIK_01415 | 1.1e-63 | XK27_00500 | L | the current gene model (or a revised gene model) may contain a | ||
KJBOBAIK_01416 | 4.3e-199 | XK27_00500 | L | the current gene model (or a revised gene model) may contain a | ||
KJBOBAIK_01417 | 4.2e-92 | S | SNARE associated Golgi protein | |||
KJBOBAIK_01418 | 2.9e-156 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
KJBOBAIK_01419 | 3.7e-102 | L | Integrase | |||
KJBOBAIK_01420 | 3.6e-69 | T | Toxin-antitoxin system, toxin component, MazF family | |||
KJBOBAIK_01421 | 1.3e-30 | |||||
KJBOBAIK_01422 | 1.8e-93 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
KJBOBAIK_01423 | 5.2e-68 | L | haloacid dehalogenase-like hydrolase | |||
KJBOBAIK_01424 | 4e-37 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
KJBOBAIK_01425 | 4.1e-128 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
KJBOBAIK_01426 | 1.1e-83 | dps | P | Belongs to the Dps family | ||
KJBOBAIK_01427 | 5.5e-272 | pipD | E | Dipeptidase | ||
KJBOBAIK_01428 | 8.3e-101 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
KJBOBAIK_01429 | 3.3e-176 | hrtB | V | ABC transporter permease | ||
KJBOBAIK_01430 | 3.2e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
KJBOBAIK_01431 | 6.7e-56 | G | phosphoglycerate mutase | |||
KJBOBAIK_01432 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
KJBOBAIK_01433 | 2.2e-165 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
KJBOBAIK_01434 | 2.6e-236 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
KJBOBAIK_01435 | 1.6e-117 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
KJBOBAIK_01436 | 8.5e-78 | rssA | S | Phospholipase, patatin family | ||
KJBOBAIK_01437 | 3.1e-30 | rssA | S | Phospholipase, patatin family | ||
KJBOBAIK_01438 | 7.8e-146 | S | hydrolase | |||
KJBOBAIK_01439 | 2.3e-144 | V | ABC transporter, ATP-binding protein | |||
KJBOBAIK_01440 | 3.8e-137 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
KJBOBAIK_01441 | 2.3e-47 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
KJBOBAIK_01442 | 7.5e-23 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
KJBOBAIK_01443 | 6.5e-64 | L | RelB antitoxin | |||
KJBOBAIK_01444 | 1.1e-75 | V | ABC transporter transmembrane region | |||
KJBOBAIK_01445 | 1.2e-205 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
KJBOBAIK_01446 | 1.4e-112 | |||||
KJBOBAIK_01447 | 2.4e-201 | yibE | S | overlaps another CDS with the same product name | ||
KJBOBAIK_01448 | 4.9e-129 | yibF | S | overlaps another CDS with the same product name | ||
KJBOBAIK_01449 | 9.7e-144 | I | alpha/beta hydrolase fold | |||
KJBOBAIK_01451 | 2.8e-26 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
KJBOBAIK_01453 | 5.4e-84 | S | ECF transporter, substrate-specific component | |||
KJBOBAIK_01454 | 5.6e-127 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
KJBOBAIK_01455 | 8.4e-45 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
KJBOBAIK_01456 | 6e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
KJBOBAIK_01457 | 3.5e-43 | aspC | 2.6.1.1 | E | Aminotransferase | |
KJBOBAIK_01458 | 9e-127 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
KJBOBAIK_01459 | 2.7e-174 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
KJBOBAIK_01460 | 2e-64 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
KJBOBAIK_01461 | 3.7e-250 | lctP | C | L-lactate permease | ||
KJBOBAIK_01462 | 1.3e-111 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
KJBOBAIK_01463 | 1.5e-51 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
KJBOBAIK_01464 | 2.9e-251 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KJBOBAIK_01465 | 6.7e-170 | |||||
KJBOBAIK_01466 | 1.4e-147 | glnA | 6.3.1.2 | E | glutamine synthetase | |
KJBOBAIK_01467 | 0.0 | oppA | E | ABC transporter | ||
KJBOBAIK_01468 | 6.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
KJBOBAIK_01469 | 7.4e-20 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
KJBOBAIK_01470 | 6.4e-51 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
KJBOBAIK_01471 | 7.4e-97 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
KJBOBAIK_01472 | 1e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
KJBOBAIK_01473 | 1.6e-161 | htrA | 3.4.21.107 | O | serine protease | |
KJBOBAIK_01474 | 4.1e-147 | vicX | 3.1.26.11 | S | domain protein | |
KJBOBAIK_01475 | 1e-148 | yycI | S | YycH protein | ||
KJBOBAIK_01476 | 1.6e-257 | yycH | S | YycH protein | ||
KJBOBAIK_01477 | 8.4e-305 | vicK | 2.7.13.3 | T | Histidine kinase | |
KJBOBAIK_01478 | 4.8e-131 | K | response regulator | |||
KJBOBAIK_01480 | 4.9e-34 | |||||
KJBOBAIK_01482 | 3.9e-147 | arbV | 2.3.1.51 | I | Acyl-transferase | |
KJBOBAIK_01483 | 1.5e-102 | srtA | 3.4.22.70 | M | sortase family | |
KJBOBAIK_01484 | 3.3e-101 | 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 | ||
KJBOBAIK_01485 | 5.1e-128 | 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 | ||
KJBOBAIK_01486 | 2.6e-61 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
KJBOBAIK_01487 | 2.9e-165 | xerD | D | recombinase XerD | ||
KJBOBAIK_01488 | 9.8e-166 | cvfB | S | S1 domain | ||
KJBOBAIK_01489 | 1.2e-186 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
KJBOBAIK_01490 | 1.2e-147 | S | cog cog1373 | |||
KJBOBAIK_01491 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
KJBOBAIK_01492 | 2e-91 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
KJBOBAIK_01493 | 2e-136 | emrY | EGP | Major facilitator Superfamily | ||
KJBOBAIK_01494 | 1.5e-152 | |||||
KJBOBAIK_01495 | 3e-24 | |||||
KJBOBAIK_01496 | 2e-30 | ywzB | S | Protein of unknown function (DUF1146) | ||
KJBOBAIK_01497 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
KJBOBAIK_01498 | 2.4e-238 | 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 | |
KJBOBAIK_01499 | 1.2e-129 | 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 | ||
KJBOBAIK_01500 | 5.7e-132 | 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) | |
KJBOBAIK_01501 | 1e-170 | yegS | 2.7.1.107 | G | Lipid kinase | |
KJBOBAIK_01502 | 2.3e-15 | ybhL | S | Belongs to the BI1 family | ||
KJBOBAIK_01503 | 1.4e-31 | O | OsmC-like protein | |||
KJBOBAIK_01505 | 1.5e-36 | oppA | E | ABC transporter substrate-binding protein | ||
KJBOBAIK_01506 | 2.1e-54 | pepN | 3.4.11.2 | E | aminopeptidase | |
KJBOBAIK_01507 | 7.3e-35 | S | Putative adhesin | |||
KJBOBAIK_01508 | 2e-223 | pbuG | S | permease | ||
KJBOBAIK_01509 | 2e-146 | S | haloacid dehalogenase-like hydrolase | |||
KJBOBAIK_01510 | 5.3e-226 | S | cog cog1373 | |||
KJBOBAIK_01511 | 1.8e-60 | K | Transcriptional regulator | |||
KJBOBAIK_01512 | 1.9e-83 | K | Transcriptional regulator | |||
KJBOBAIK_01513 | 4.3e-127 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
KJBOBAIK_01514 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
KJBOBAIK_01515 | 4.8e-168 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
KJBOBAIK_01516 | 5.7e-26 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
KJBOBAIK_01517 | 2.7e-57 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
KJBOBAIK_01518 | 1.1e-90 | yutD | S | Protein of unknown function (DUF1027) | ||
KJBOBAIK_01519 | 1.5e-112 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
KJBOBAIK_01520 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
KJBOBAIK_01521 | 7.7e-94 | dedA | S | SNARE-like domain protein | ||
KJBOBAIK_01522 | 2e-103 | S | TPM domain | |||
KJBOBAIK_01523 | 1.8e-89 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
KJBOBAIK_01524 | 3.7e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
KJBOBAIK_01525 | 1.2e-111 | E | Belongs to the SOS response-associated peptidase family | |||
KJBOBAIK_01527 | 7.9e-112 | |||||
KJBOBAIK_01528 | 1.7e-29 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
KJBOBAIK_01529 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
KJBOBAIK_01530 | 2.1e-262 | E | ABC transporter, substratebinding protein | |||
KJBOBAIK_01531 | 9.1e-10 | K | peptidyl-tyrosine sulfation | |||
KJBOBAIK_01533 | 4.2e-129 | S | interspecies interaction between organisms | |||
KJBOBAIK_01534 | 2.7e-34 | |||||
KJBOBAIK_01537 | 6.6e-176 | uvrA3 | L | excinuclease ABC, A subunit | ||
KJBOBAIK_01538 | 1.4e-40 | C | Flavodoxin | |||
KJBOBAIK_01539 | 3.2e-170 | ylbL | T | Belongs to the peptidase S16 family | ||
KJBOBAIK_01540 | 4.5e-78 | comEA | L | Competence protein ComEA | ||
KJBOBAIK_01541 | 3e-102 | S | SLAP domain | |||
KJBOBAIK_01542 | 4.3e-40 | S | Protein of unknown function (DUF2922) | |||
KJBOBAIK_01543 | 5.5e-30 | |||||
KJBOBAIK_01545 | 2.7e-34 | S | YSIRK type signal peptide | |||
KJBOBAIK_01546 | 5.1e-108 | F | DNA/RNA non-specific endonuclease | |||
KJBOBAIK_01547 | 1.1e-14 | mrr | L | restriction endonuclease | ||
KJBOBAIK_01548 | 2e-75 | S | cog cog0433 | |||
KJBOBAIK_01549 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
KJBOBAIK_01550 | 4.4e-09 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
KJBOBAIK_01551 | 7.8e-149 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
KJBOBAIK_01552 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
KJBOBAIK_01553 | 4e-176 | mreB | D | cell shape determining protein MreB | ||
KJBOBAIK_01554 | 5e-108 | radC | L | DNA repair protein | ||
KJBOBAIK_01555 | 3.1e-101 | S | Haloacid dehalogenase-like hydrolase | |||
KJBOBAIK_01556 | 6.5e-24 | pstA | P | Phosphate transport system permease protein PstA | ||
KJBOBAIK_01557 | 1.1e-144 | 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 | |
KJBOBAIK_01558 | 3.1e-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 | |
KJBOBAIK_01559 | 2.2e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
KJBOBAIK_01560 | 2.4e-62 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
KJBOBAIK_01561 | 1.1e-147 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
KJBOBAIK_01562 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
KJBOBAIK_01563 | 2.6e-36 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
KJBOBAIK_01564 | 1e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
KJBOBAIK_01565 | 4.3e-65 | nhaC | C | Na H antiporter NhaC | ||
KJBOBAIK_01566 | 1.4e-147 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
KJBOBAIK_01567 | 2.6e-57 | |||||
KJBOBAIK_01568 | 7.9e-92 | pbuG | S | permease | ||
KJBOBAIK_01569 | 2.5e-40 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
KJBOBAIK_01570 | 3.1e-16 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
KJBOBAIK_01571 | 5.4e-48 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | ||
KJBOBAIK_01572 | 7.6e-23 | 1.1.1.100 | S | KR domain | ||
KJBOBAIK_01573 | 1.7e-16 | ymfI | 1.1.1.100, 1.3.1.28 | S | oxidoreductase activity | |
KJBOBAIK_01574 | 1.5e-56 | asp | S | Asp23 family, cell envelope-related function | ||
KJBOBAIK_01575 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
KJBOBAIK_01577 | 1.8e-87 | M | hydrolase, family 25 | |||
KJBOBAIK_01578 | 5.8e-39 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
KJBOBAIK_01579 | 6e-289 | 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 | ||
KJBOBAIK_01580 | 6.5e-82 | bcgIB | 2.1.1.72, 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
KJBOBAIK_01581 | 8.2e-226 | V | N-6 DNA Methylase | |||
KJBOBAIK_01582 | 1.7e-124 | dnaK | O | Heat shock 70 kDa protein | ||
KJBOBAIK_01583 | 2.2e-182 | dnaK | O | Heat shock 70 kDa protein | ||
KJBOBAIK_01584 | 8e-68 | 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 | ||
KJBOBAIK_01585 | 3.2e-192 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
KJBOBAIK_01586 | 3.2e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
KJBOBAIK_01587 | 4.3e-153 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
KJBOBAIK_01588 | 1.9e-59 | 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 | ||
KJBOBAIK_01589 | 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 | ||
KJBOBAIK_01590 | 5.6e-255 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
KJBOBAIK_01591 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
KJBOBAIK_01592 | 2.6e-146 | S | Calcineurin-like phosphoesterase | |||
KJBOBAIK_01593 | 7.2e-183 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
KJBOBAIK_01594 | 1.2e-23 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KJBOBAIK_01595 | 9.1e-09 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
KJBOBAIK_01596 | 4.1e-156 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
KJBOBAIK_01597 | 2.6e-65 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
KJBOBAIK_01598 | 1.1e-20 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_01599 | 1.4e-10 | |||||
KJBOBAIK_01600 | 2.8e-65 | K | LytTr DNA-binding domain | |||
KJBOBAIK_01601 | 1.2e-49 | S | Protein of unknown function (DUF3021) | |||
KJBOBAIK_01602 | 6.3e-105 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
KJBOBAIK_01603 | 6e-70 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
KJBOBAIK_01604 | 4.6e-28 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
KJBOBAIK_01605 | 2.7e-132 | S | membrane transporter protein | |||
KJBOBAIK_01606 | 6.9e-81 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
KJBOBAIK_01607 | 4.3e-25 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
KJBOBAIK_01608 | 1.5e-127 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
KJBOBAIK_01609 | 5.3e-116 | P | ABC transporter permease | |||
KJBOBAIK_01610 | 6.2e-32 | csaB | M | Glycosyl transferases group 1 | ||
KJBOBAIK_01611 | 4.6e-218 | scrB | 3.2.1.26 | GH32 | G | invertase |
KJBOBAIK_01612 | 6e-97 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
KJBOBAIK_01613 | 6.7e-110 | rfbP | M | Bacterial sugar transferase | ||
KJBOBAIK_01614 | 1.9e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
KJBOBAIK_01616 | 1.4e-73 | ftsZ | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
KJBOBAIK_01617 | 2e-116 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
KJBOBAIK_01618 | 7.5e-230 | oppA | E | ABC transporter substrate-binding protein | ||
KJBOBAIK_01619 | 8.6e-97 | oppA | E | ABC transporter substrate-binding protein | ||
KJBOBAIK_01620 | 1.4e-176 | K | AI-2E family transporter | |||
KJBOBAIK_01621 | 2.6e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
KJBOBAIK_01622 | 4.1e-18 | |||||
KJBOBAIK_01623 | 5.2e-248 | G | Major Facilitator | |||
KJBOBAIK_01624 | 2.4e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
KJBOBAIK_01625 | 8.2e-23 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
KJBOBAIK_01626 | 6.3e-89 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
KJBOBAIK_01627 | 2.1e-152 | ABC-SBP | S | ABC transporter | ||
KJBOBAIK_01628 | 2.8e-131 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
KJBOBAIK_01629 | 9.8e-144 | P | CorA-like Mg2+ transporter protein | |||
KJBOBAIK_01630 | 3.5e-160 | yvgN | C | Aldo keto reductase | ||
KJBOBAIK_01631 | 5.6e-121 | 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 | ||
KJBOBAIK_01632 | 5.4e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
KJBOBAIK_01633 | 4.1e-67 | |||||
KJBOBAIK_01634 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
KJBOBAIK_01635 | 1.4e-124 | M | Glycosyl hydrolases family 25 | |||
KJBOBAIK_01636 | 1.6e-143 | ylbM | S | Belongs to the UPF0348 family | ||
KJBOBAIK_01637 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
KJBOBAIK_01638 | 1.2e-126 | K | response regulator | |||
KJBOBAIK_01639 | 2.8e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
KJBOBAIK_01640 | 1e-12 | |||||
KJBOBAIK_01641 | 1.5e-97 | S | CAAX protease self-immunity | |||
KJBOBAIK_01642 | 6.1e-224 | S | SLAP domain | |||
KJBOBAIK_01643 | 1e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
KJBOBAIK_01644 | 3.7e-207 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
KJBOBAIK_01645 | 9.3e-63 | ybiR | P | Citrate transporter | ||
KJBOBAIK_01646 | 5.1e-96 | lemA | S | LemA family | ||
KJBOBAIK_01647 | 1.9e-133 | htpX | O | Belongs to the peptidase M48B family | ||
KJBOBAIK_01648 | 7.9e-174 | K | helix_turn_helix, arabinose operon control protein | |||
KJBOBAIK_01649 | 1.1e-248 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
KJBOBAIK_01650 | 2.8e-77 | P | Cobalt transport protein | |||
KJBOBAIK_01651 | 1.8e-172 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
KJBOBAIK_01652 | 6.5e-91 | G | Peptidase_C39 like family | |||
KJBOBAIK_01653 | 8.3e-162 | M | NlpC/P60 family | |||
KJBOBAIK_01654 | 8.4e-25 | G | Peptidase_C39 like family | |||
KJBOBAIK_01655 | 5.3e-14 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
KJBOBAIK_01656 | 3.1e-80 | mutT | 3.6.1.55 | F | NUDIX domain | |
KJBOBAIK_01657 | 1.4e-127 | S | Peptidase family M23 | |||
KJBOBAIK_01658 | 1.2e-180 | 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 | ||
KJBOBAIK_01659 | 2.8e-90 | L | An automated process has identified a potential problem with this gene model | |||
KJBOBAIK_01660 | 1.5e-11 | GT2,GT4 | M | family 8 | ||
KJBOBAIK_01661 | 1.1e-50 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
KJBOBAIK_01662 | 1.8e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
KJBOBAIK_01663 | 8.7e-140 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
KJBOBAIK_01664 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
KJBOBAIK_01665 | 9e-26 | |||||
KJBOBAIK_01666 | 2.1e-88 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
KJBOBAIK_01667 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
KJBOBAIK_01668 | 5.7e-106 | 2.4.1.58 | GT8 | M | family 8 | |
KJBOBAIK_01669 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
KJBOBAIK_01670 | 8.2e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
KJBOBAIK_01671 | 1.6e-108 | 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 | ||
KJBOBAIK_01672 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
KJBOBAIK_01673 | 2e-36 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
KJBOBAIK_01674 | 5.7e-28 | rarA | L | recombination factor protein RarA | ||
KJBOBAIK_01675 | 8.4e-39 | |||||
KJBOBAIK_01676 | 1.8e-78 | usp6 | T | universal stress protein | ||
KJBOBAIK_01677 | 7.3e-209 | rodA | D | Belongs to the SEDS family | ||
KJBOBAIK_01678 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
KJBOBAIK_01679 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
KJBOBAIK_01680 | 1.2e-67 | mbl | D | Cell shape determining protein MreB Mrl | ||
KJBOBAIK_01681 | 9e-98 | |||||
KJBOBAIK_01682 | 4.9e-108 | K | LysR substrate binding domain | |||
KJBOBAIK_01683 | 1e-20 | |||||
KJBOBAIK_01684 | 3e-112 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
KJBOBAIK_01685 | 2.3e-70 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
KJBOBAIK_01686 | 1.8e-58 | S | Putative adhesin | |||
KJBOBAIK_01687 | 5.6e-101 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
KJBOBAIK_01688 | 3.2e-13 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
KJBOBAIK_01689 | 1.4e-178 | sip | L | Belongs to the 'phage' integrase family | ||
KJBOBAIK_01690 | 1.6e-20 | S | YjcQ protein | |||
KJBOBAIK_01695 | 3.3e-18 | S | Pfam:Peptidase_M78 | |||
KJBOBAIK_01696 | 2.5e-22 | K | Cro/C1-type HTH DNA-binding domain | |||
KJBOBAIK_01697 | 9.5e-12 | K | Helix-turn-helix XRE-family like proteins | |||
KJBOBAIK_01698 | 2.5e-30 | K | BRO family, N-terminal domain | |||
KJBOBAIK_01700 | 2e-70 | S | Iron-sulphur cluster biosynthesis | |||
KJBOBAIK_01701 | 1.9e-309 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
KJBOBAIK_01702 | 1.2e-17 | |||||
KJBOBAIK_01703 | 1.1e-07 | S | Uncharacterised protein family (UPF0236) | |||
KJBOBAIK_01704 | 1.3e-188 | ydaM | M | Glycosyl transferase | ||
KJBOBAIK_01705 | 1.2e-173 | G | Glycosyl hydrolases family 8 | |||
KJBOBAIK_01706 | 1e-119 | yfbR | S | HD containing hydrolase-like enzyme | ||
KJBOBAIK_01707 | 6.4e-159 | L | HNH nucleases | |||
KJBOBAIK_01709 | 4.1e-180 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
KJBOBAIK_01710 | 1.4e-86 | C | Aldo keto reductase | |||
KJBOBAIK_01711 | 3.8e-48 | M | LysM domain protein | |||
KJBOBAIK_01712 | 2.6e-132 | czcD | P | cation diffusion facilitator family transporter | ||
KJBOBAIK_01713 | 1.4e-23 | |||||
KJBOBAIK_01714 | 1.7e-125 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
KJBOBAIK_01715 | 3.5e-182 | S | AAA domain | |||
KJBOBAIK_01716 | 7.3e-44 | |||||
KJBOBAIK_01717 | 1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
KJBOBAIK_01718 | 4.1e-52 | |||||
KJBOBAIK_01719 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
KJBOBAIK_01720 | 7.8e-78 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
KJBOBAIK_01722 | 2.3e-102 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
KJBOBAIK_01723 | 8.8e-110 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
KJBOBAIK_01724 | 2e-19 | |||||
KJBOBAIK_01725 | 1.7e-99 | L | Helix-turn-helix domain | |||
KJBOBAIK_01726 | 2.3e-157 | L | hmm pf00665 | |||
KJBOBAIK_01728 | 3.7e-27 | 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 | ||
KJBOBAIK_01729 | 3.5e-101 | ylbE | GM | NAD(P)H-binding | ||
KJBOBAIK_01730 | 7.6e-94 | S | VanZ like family | |||
KJBOBAIK_01731 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
KJBOBAIK_01732 | 1.1e-36 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KJBOBAIK_01733 | 4.6e-145 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
KJBOBAIK_01734 | 5.6e-195 | rny | S | Endoribonuclease that initiates mRNA decay |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)