ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
JHHLHNBC_00002 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_00003 | 2.8e-171 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
JHHLHNBC_00004 | 3e-228 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
JHHLHNBC_00005 | 2e-31 | yajC | U | Preprotein translocase | ||
JHHLHNBC_00006 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
JHHLHNBC_00007 | 3e-116 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
JHHLHNBC_00008 | 3.7e-85 | gldA | 1.1.1.1, 1.1.1.6 | C | dehydrogenase | |
JHHLHNBC_00011 | 2.3e-226 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
JHHLHNBC_00012 | 2.6e-80 | S | Threonine/Serine exporter, ThrE | |||
JHHLHNBC_00013 | 1.9e-133 | thrE | S | Putative threonine/serine exporter | ||
JHHLHNBC_00015 | 1.3e-31 | |||||
JHHLHNBC_00016 | 1e-274 | V | ABC transporter transmembrane region | |||
JHHLHNBC_00018 | 1e-284 | 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 | ||
JHHLHNBC_00019 | 4.6e-50 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
JHHLHNBC_00020 | 6.7e-23 | S | Protein of unknown function (DUF4065) | |||
JHHLHNBC_00023 | 1.6e-85 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
JHHLHNBC_00024 | 7.1e-274 | 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 | ||
JHHLHNBC_00025 | 3.2e-217 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
JHHLHNBC_00026 | 1e-226 | 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 | |
JHHLHNBC_00027 | 1.2e-115 | rex | K | CoA binding domain | ||
JHHLHNBC_00028 | 1.3e-212 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
JHHLHNBC_00029 | 4.2e-258 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
JHHLHNBC_00030 | 1.1e-112 | dnaD | L | DnaD domain protein | ||
JHHLHNBC_00031 | 9.7e-115 | 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 | |
JHHLHNBC_00032 | 2.3e-86 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
JHHLHNBC_00033 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
JHHLHNBC_00034 | 3.3e-120 | 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 | ||
JHHLHNBC_00035 | 6.2e-105 | ypsA | S | Belongs to the UPF0398 family | ||
JHHLHNBC_00036 | 6.1e-246 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
JHHLHNBC_00037 | 7.8e-85 | yslB | S | Protein of unknown function (DUF2507) | ||
JHHLHNBC_00038 | 2.3e-176 | 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) | |
JHHLHNBC_00039 | 3.2e-53 | nudA | S | ASCH | ||
JHHLHNBC_00040 | 2.5e-77 | |||||
JHHLHNBC_00041 | 1.4e-60 | 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 | ||
JHHLHNBC_00042 | 2e-178 | S | DUF218 domain | |||
JHHLHNBC_00043 | 2.4e-83 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
JHHLHNBC_00044 | 3.3e-266 | ywfO | S | HD domain protein | ||
JHHLHNBC_00045 | 4.6e-157 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
JHHLHNBC_00046 | 3.5e-79 | ywiB | S | Domain of unknown function (DUF1934) | ||
JHHLHNBC_00047 | 1.2e-154 | 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 | |
JHHLHNBC_00048 | 2e-166 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
JHHLHNBC_00049 | 5.3e-167 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
JHHLHNBC_00050 | 7.2e-155 | 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 | |
JHHLHNBC_00051 | 1.1e-169 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
JHHLHNBC_00052 | 4.4e-169 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
JHHLHNBC_00053 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
JHHLHNBC_00054 | 1.3e-75 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
JHHLHNBC_00055 | 1.2e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
JHHLHNBC_00056 | 8.6e-184 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
JHHLHNBC_00057 | 3.1e-216 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
JHHLHNBC_00058 | 4.4e-228 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
JHHLHNBC_00059 | 8.8e-142 | mreB | D | cell shape determining protein MreB | ||
JHHLHNBC_00060 | 5.6e-169 | gbuC | E | glycine betaine | ||
JHHLHNBC_00061 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_00062 | 2.6e-65 | gtcA | S | Teichoic acid glycosylation protein | ||
JHHLHNBC_00063 | 1.1e-127 | srtA | 3.4.22.70 | M | Sortase family | |
JHHLHNBC_00064 | 1.3e-180 | K | AI-2E family transporter | |||
JHHLHNBC_00065 | 1.8e-198 | pbpX1 | V | Beta-lactamase | ||
JHHLHNBC_00066 | 9.2e-123 | S | zinc-ribbon domain | |||
JHHLHNBC_00067 | 4.4e-29 | |||||
JHHLHNBC_00068 | 3.2e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
JHHLHNBC_00069 | 7.3e-138 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
JHHLHNBC_00070 | 2.4e-136 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
JHHLHNBC_00072 | 4.2e-156 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
JHHLHNBC_00073 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
JHHLHNBC_00074 | 4.7e-171 | ccpB | 5.1.1.1 | K | lacI family | |
JHHLHNBC_00075 | 1.5e-68 | |||||
JHHLHNBC_00076 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
JHHLHNBC_00077 | 1.5e-106 | rsmC | 2.1.1.172 | J | Methyltransferase | |
JHHLHNBC_00078 | 4.7e-49 | |||||
JHHLHNBC_00079 | 7.5e-86 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
JHHLHNBC_00080 | 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 | |
JHHLHNBC_00081 | 1.5e-33 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
JHHLHNBC_00082 | 5.6e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
JHHLHNBC_00083 | 8.7e-38 | S | Protein of unknown function (DUF2508) | |||
JHHLHNBC_00084 | 7.4e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
JHHLHNBC_00085 | 7.8e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
JHHLHNBC_00086 | 1.6e-162 | akr5f | 1.1.1.346 | S | reductase | |
JHHLHNBC_00087 | 4.6e-70 | adhR | K | helix_turn_helix, mercury resistance | ||
JHHLHNBC_00088 | 4.8e-83 | bioY | S | BioY family | ||
JHHLHNBC_00089 | 2.2e-63 | |||||
JHHLHNBC_00090 | 7.7e-224 | queG | 1.17.99.6 | C | Domain of unknown function (DUF1730) | |
JHHLHNBC_00091 | 2.8e-132 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
JHHLHNBC_00092 | 3.3e-65 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_00093 | 1.9e-77 | usp5 | T | universal stress protein | ||
JHHLHNBC_00095 | 2.8e-111 | tag | 3.2.2.20 | L | glycosylase | |
JHHLHNBC_00096 | 4.2e-156 | EG | EamA-like transporter family | |||
JHHLHNBC_00097 | 1.5e-25 | |||||
JHHLHNBC_00098 | 1.1e-86 | |||||
JHHLHNBC_00099 | 7.1e-39 | |||||
JHHLHNBC_00100 | 1.8e-187 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
JHHLHNBC_00101 | 6.7e-240 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
JHHLHNBC_00102 | 7.4e-138 | bceA | V | ABC transporter | ||
JHHLHNBC_00103 | 0.0 | V | ABC transporter (permease) | |||
JHHLHNBC_00104 | 7.6e-91 | traP | 1.14.99.57, 6.2.1.3 | S | Antibiotic biosynthesis monooxygenase | |
JHHLHNBC_00105 | 1.9e-138 | yhfI | S | Metallo-beta-lactamase superfamily | ||
JHHLHNBC_00106 | 1.5e-65 | 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 | |
JHHLHNBC_00107 | 5.1e-122 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
JHHLHNBC_00108 | 4.1e-304 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
JHHLHNBC_00109 | 1.2e-177 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
JHHLHNBC_00110 | 2.9e-16 | |||||
JHHLHNBC_00111 | 1.2e-67 | |||||
JHHLHNBC_00112 | 5.6e-211 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
JHHLHNBC_00113 | 1.1e-134 | S | E1-E2 ATPase | |||
JHHLHNBC_00114 | 4.9e-99 | 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 | |
JHHLHNBC_00115 | 2.8e-52 | |||||
JHHLHNBC_00117 | 4.9e-31 | ykzG | S | Belongs to the UPF0356 family | ||
JHHLHNBC_00118 | 1.1e-37 | veg | S | Biofilm formation stimulator VEG | ||
JHHLHNBC_00119 | 1.4e-164 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
JHHLHNBC_00120 | 6.7e-159 | czcD | P | cation diffusion facilitator family transporter | ||
JHHLHNBC_00121 | 1.8e-123 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
JHHLHNBC_00122 | 6.5e-119 | ybbL | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00123 | 1.3e-151 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
JHHLHNBC_00124 | 7.6e-222 | ysaA | V | RDD family | ||
JHHLHNBC_00125 | 5.1e-214 | 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 | |
JHHLHNBC_00126 | 2.1e-285 | G | MFS/sugar transport protein | |||
JHHLHNBC_00127 | 0.0 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase concanavalin-like domain | ||
JHHLHNBC_00128 | 1.6e-169 | ssuA | P | NMT1-like family | ||
JHHLHNBC_00129 | 1.6e-293 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
JHHLHNBC_00130 | 1.7e-232 | yfiQ | I | Acyltransferase family | ||
JHHLHNBC_00131 | 1.1e-119 | ssuB | P | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_00132 | 3.9e-145 | ssuC | U | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_00133 | 3.8e-122 | S | B3/4 domain | |||
JHHLHNBC_00134 | 0.0 | V | ABC transporter | |||
JHHLHNBC_00135 | 0.0 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_00136 | 1e-210 | EGP | Transmembrane secretion effector | |||
JHHLHNBC_00137 | 1e-96 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
JHHLHNBC_00138 | 2.5e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_00139 | 3.3e-80 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
JHHLHNBC_00140 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
JHHLHNBC_00141 | 5.7e-50 | S | Family of unknown function (DUF5322) | |||
JHHLHNBC_00143 | 1.2e-103 | |||||
JHHLHNBC_00144 | 3.6e-129 | |||||
JHHLHNBC_00145 | 2.5e-77 | copR | K | Copper transport repressor CopY TcrY | ||
JHHLHNBC_00146 | 2.6e-217 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
JHHLHNBC_00147 | 3.3e-180 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
JHHLHNBC_00148 | 2.4e-22 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
JHHLHNBC_00149 | 2.7e-163 | S | Tetratricopeptide repeat | |||
JHHLHNBC_00150 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
JHHLHNBC_00151 | 4.8e-120 | |||||
JHHLHNBC_00153 | 7e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
JHHLHNBC_00154 | 3.5e-143 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
JHHLHNBC_00155 | 2.4e-46 | yktA | S | Belongs to the UPF0223 family | ||
JHHLHNBC_00156 | 2.3e-146 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
JHHLHNBC_00157 | 4.1e-259 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
JHHLHNBC_00158 | 6.4e-256 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
JHHLHNBC_00159 | 4.3e-138 | yacL | S | domain protein | ||
JHHLHNBC_00160 | 3.1e-103 | K | sequence-specific DNA binding | |||
JHHLHNBC_00161 | 8.4e-154 | V | ABC transporter, ATP-binding protein | |||
JHHLHNBC_00162 | 3.3e-133 | S | ABC-2 family transporter protein | |||
JHHLHNBC_00163 | 9.9e-198 | inlJ | M | MucBP domain | ||
JHHLHNBC_00164 | 8.8e-145 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
JHHLHNBC_00165 | 1.6e-137 | yacL | S | domain protein | ||
JHHLHNBC_00166 | 4.9e-222 | inlJ | M | MucBP domain | ||
JHHLHNBC_00167 | 2.8e-61 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
JHHLHNBC_00168 | 7.7e-131 | S | Membrane | |||
JHHLHNBC_00169 | 1.2e-141 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
JHHLHNBC_00170 | 1.1e-15 | |||||
JHHLHNBC_00171 | 1.2e-113 | 3.1.21.3 | V | Type I restriction | ||
JHHLHNBC_00172 | 2.2e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
JHHLHNBC_00173 | 1.4e-230 | 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 | |
JHHLHNBC_00174 | 1.8e-251 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
JHHLHNBC_00175 | 1.3e-137 | jag | S | R3H domain protein | ||
JHHLHNBC_00176 | 6.9e-237 | rarA | L | recombination factor protein RarA | ||
JHHLHNBC_00177 | 3.5e-174 | prmA | J | Ribosomal protein L11 methyltransferase | ||
JHHLHNBC_00178 | 3.6e-85 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
JHHLHNBC_00179 | 3.2e-112 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
JHHLHNBC_00180 | 3.1e-37 | |||||
JHHLHNBC_00181 | 2.7e-64 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_00182 | 2.3e-26 | |||||
JHHLHNBC_00183 | 2.9e-62 | |||||
JHHLHNBC_00185 | 9.2e-112 | 1.6.5.2 | S | Flavodoxin-like fold | ||
JHHLHNBC_00186 | 2.1e-94 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_00187 | 2.7e-114 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
JHHLHNBC_00188 | 1.7e-148 | potB | P | ABC transporter permease | ||
JHHLHNBC_00189 | 8.9e-145 | potC | P | ABC transporter permease | ||
JHHLHNBC_00190 | 1.6e-207 | potD | P | ABC transporter | ||
JHHLHNBC_00191 | 6.8e-14 | T | SpoVT / AbrB like domain | |||
JHHLHNBC_00193 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
JHHLHNBC_00194 | 6.6e-82 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
JHHLHNBC_00195 | 2.9e-117 | K | Transcriptional regulator | |||
JHHLHNBC_00196 | 4.9e-186 | V | ABC transporter | |||
JHHLHNBC_00197 | 3.9e-128 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_00198 | 1e-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 | |
JHHLHNBC_00199 | 2.9e-88 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
JHHLHNBC_00200 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
JHHLHNBC_00201 | 1.3e-14 | |||||
JHHLHNBC_00202 | 1.1e-47 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_00203 | 3e-173 | amiD | P | N-terminal TM domain of oligopeptide transport permease C | ||
JHHLHNBC_00204 | 4.4e-49 | |||||
JHHLHNBC_00205 | 1e-209 | |||||
JHHLHNBC_00206 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
JHHLHNBC_00207 | 0.0 | oppA1 | E | ABC transporter substrate-binding protein | ||
JHHLHNBC_00208 | 1.7e-125 | 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 | |
JHHLHNBC_00209 | 0.0 | oppA1 | E | ABC transporter substrate-binding protein | ||
JHHLHNBC_00210 | 7.7e-126 | 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 | |
JHHLHNBC_00211 | 3.4e-61 | |||||
JHHLHNBC_00212 | 1.6e-293 | |||||
JHHLHNBC_00214 | 1.9e-197 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
JHHLHNBC_00215 | 4e-59 | hxlR | K | Transcriptional regulator, HxlR family | ||
JHHLHNBC_00216 | 1.5e-127 | S | membrane transporter protein | |||
JHHLHNBC_00217 | 5.9e-200 | |||||
JHHLHNBC_00218 | 1.2e-129 | XK27_12140 | V | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_00219 | 2.5e-300 | S | Psort location CytoplasmicMembrane, score | |||
JHHLHNBC_00220 | 7.5e-126 | K | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_00221 | 1.3e-196 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
JHHLHNBC_00222 | 2.2e-157 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_00223 | 2.2e-199 | |||||
JHHLHNBC_00224 | 8e-106 | |||||
JHHLHNBC_00225 | 1.7e-07 | |||||
JHHLHNBC_00226 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
JHHLHNBC_00227 | 2.4e-275 | ycaM | E | amino acid | ||
JHHLHNBC_00228 | 1.3e-238 | G | MFS/sugar transport protein | |||
JHHLHNBC_00229 | 7.6e-91 | S | Protein of unknown function (DUF1440) | |||
JHHLHNBC_00230 | 6.7e-161 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
JHHLHNBC_00231 | 6.8e-192 | yghZ | C | Aldo keto reductase family protein | ||
JHHLHNBC_00232 | 0.0 | uvrA3 | L | ABC transporter | ||
JHHLHNBC_00233 | 1.8e-61 | K | MarR family | |||
JHHLHNBC_00234 | 7.9e-109 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
JHHLHNBC_00236 | 2.1e-259 | V | ABC transporter transmembrane region | |||
JHHLHNBC_00237 | 1.4e-16 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
JHHLHNBC_00238 | 9.8e-39 | L | Transposase and inactivated derivatives | |||
JHHLHNBC_00239 | 2.7e-78 | L | COG3547 Transposase and inactivated derivatives | |||
JHHLHNBC_00240 | 5.9e-71 | |||||
JHHLHNBC_00242 | 1.7e-62 | |||||
JHHLHNBC_00243 | 7.2e-65 | |||||
JHHLHNBC_00244 | 0.0 | L | Protein of unknown function (DUF3991) | |||
JHHLHNBC_00246 | 5.2e-218 | 3.1.1.32, 3.1.1.4 | S | COG0790 FOG TPR repeat, SEL1 subfamily | ||
JHHLHNBC_00253 | 2.4e-181 | M | cysteine-type peptidase activity | |||
JHHLHNBC_00254 | 0.0 | trsE | S | COG0433 Predicted ATPase | ||
JHHLHNBC_00255 | 8.4e-105 | |||||
JHHLHNBC_00257 | 3.8e-221 | 5.4.99.21 | S | domain, Protein | ||
JHHLHNBC_00258 | 0.0 | U | TraM recognition site of TraD and TraG | |||
JHHLHNBC_00261 | 1.1e-201 | M | Domain of unknown function (DUF5011) | |||
JHHLHNBC_00262 | 3.9e-205 | |||||
JHHLHNBC_00263 | 5.2e-31 | |||||
JHHLHNBC_00272 | 9.4e-59 | M | Psort location Cellwall, score | |||
JHHLHNBC_00273 | 2.3e-75 | M | Peptidase_C39 like family | |||
JHHLHNBC_00275 | 8.4e-148 | M | Peptidase_C39 like family | |||
JHHLHNBC_00282 | 8.2e-87 | repA | S | Replication initiator protein A | ||
JHHLHNBC_00283 | 1.2e-93 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
JHHLHNBC_00284 | 3e-17 | S | Family of unknown function (DUF5388) | |||
JHHLHNBC_00285 | 2.5e-19 | |||||
JHHLHNBC_00286 | 9.5e-170 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
JHHLHNBC_00287 | 3.1e-23 | |||||
JHHLHNBC_00288 | 4.8e-07 | |||||
JHHLHNBC_00291 | 4.4e-115 | L | Resolvase, N terminal domain | |||
JHHLHNBC_00292 | 2e-26 | ligA | 6.5.1.2 | L | BRCA1 C Terminus (BRCT) domain | |
JHHLHNBC_00293 | 2.6e-269 | L | Transposase DDE domain | |||
JHHLHNBC_00294 | 1.1e-70 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
JHHLHNBC_00295 | 1.7e-69 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
JHHLHNBC_00296 | 2.1e-199 | 3.4.22.70 | M | Sortase family | ||
JHHLHNBC_00297 | 1.9e-181 | M | LPXTG cell wall anchor motif | |||
JHHLHNBC_00298 | 2.1e-126 | M | domain protein | |||
JHHLHNBC_00299 | 0.0 | yvcC | M | Cna protein B-type domain | ||
JHHLHNBC_00300 | 4.2e-09 | M | Collagen binding domain | |||
JHHLHNBC_00301 | 1.1e-112 | L | Integrase core domain | |||
JHHLHNBC_00302 | 2.2e-237 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
JHHLHNBC_00303 | 3.6e-49 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_00304 | 2e-227 | endOF2 | 3.2.1.14, 3.2.1.52, 3.2.1.96 | GH18,GH20 | G | chitinase activity |
JHHLHNBC_00305 | 0.0 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_00306 | 2.2e-111 | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | ||
JHHLHNBC_00307 | 6.2e-79 | 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_00308 | 1.6e-45 | sgcB | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_00309 | 5.1e-246 | G | PTS system sugar-specific permease component | |||
JHHLHNBC_00310 | 1.4e-225 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
JHHLHNBC_00311 | 1.1e-99 | |||||
JHHLHNBC_00314 | 2.5e-84 | |||||
JHHLHNBC_00315 | 1.2e-109 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_00316 | 2.1e-102 | |||||
JHHLHNBC_00317 | 4e-61 | |||||
JHHLHNBC_00318 | 2.4e-115 | |||||
JHHLHNBC_00320 | 6.9e-76 | S | CAAX protease self-immunity | |||
JHHLHNBC_00321 | 2.1e-64 | S | CAAX protease self-immunity | |||
JHHLHNBC_00322 | 0.0 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
JHHLHNBC_00323 | 1.2e-288 | rhaB | 2.7.1.5, 2.7.1.51 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
JHHLHNBC_00324 | 1.5e-231 | ywtG | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00325 | 1.1e-77 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
JHHLHNBC_00326 | 4.4e-149 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
JHHLHNBC_00327 | 7.3e-130 | fcsR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_00328 | 3e-289 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
JHHLHNBC_00329 | 2.7e-239 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_00330 | 4.5e-71 | K | Transcriptional regulator | |||
JHHLHNBC_00331 | 2.7e-16 | S | Protein conserved in bacteria | |||
JHHLHNBC_00332 | 1.3e-24 | S | Protein conserved in bacteria | |||
JHHLHNBC_00333 | 0.0 | sprD | D | Domain of Unknown Function (DUF1542) | ||
JHHLHNBC_00334 | 0.0 | sprD | D | Domain of Unknown Function (DUF1542) | ||
JHHLHNBC_00335 | 4.4e-144 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_00336 | 3.5e-122 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_00337 | 3e-130 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_00338 | 3.4e-217 | fucA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
JHHLHNBC_00339 | 8.7e-113 | K | UTRA domain | |||
JHHLHNBC_00340 | 0.0 | sprD | D | Domain of Unknown Function (DUF1542) | ||
JHHLHNBC_00341 | 1.5e-259 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
JHHLHNBC_00342 | 1.1e-128 | rpl | K | Helix-turn-helix domain, rpiR family | ||
JHHLHNBC_00343 | 8.9e-170 | pfkB | 2.7.1.11, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
JHHLHNBC_00344 | 0.0 | fruA | 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_00345 | 4.1e-158 | 5.1.3.3 | G | Aldose 1-epimerase | ||
JHHLHNBC_00346 | 1e-212 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
JHHLHNBC_00347 | 1.5e-40 | ypaA | S | Protein of unknown function (DUF1304) | ||
JHHLHNBC_00348 | 1.7e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
JHHLHNBC_00349 | 5.9e-202 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
JHHLHNBC_00350 | 8.2e-102 | 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 | ||
JHHLHNBC_00351 | 4e-75 | yqhY | S | Asp23 family, cell envelope-related function | ||
JHHLHNBC_00352 | 1.6e-67 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
JHHLHNBC_00353 | 2.5e-150 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
JHHLHNBC_00354 | 3.2e-245 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
JHHLHNBC_00355 | 3.9e-31 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
JHHLHNBC_00356 | 9.6e-147 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JHHLHNBC_00357 | 7.5e-152 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
JHHLHNBC_00358 | 1.5e-74 | argR | K | Regulates arginine biosynthesis genes | ||
JHHLHNBC_00359 | 8e-310 | recN | L | May be involved in recombinational repair of damaged DNA | ||
JHHLHNBC_00360 | 7.4e-41 | |||||
JHHLHNBC_00361 | 8.4e-125 | rssA | S | Patatin-like phospholipase | ||
JHHLHNBC_00362 | 8.5e-116 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
JHHLHNBC_00363 | 5.9e-36 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
JHHLHNBC_00364 | 2.1e-211 | 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 | |
JHHLHNBC_00365 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
JHHLHNBC_00366 | 5.9e-177 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
JHHLHNBC_00367 | 4.2e-253 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
JHHLHNBC_00368 | 4.4e-135 | stp | 3.1.3.16 | T | phosphatase | |
JHHLHNBC_00369 | 3.4e-195 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
JHHLHNBC_00370 | 2.6e-140 | ksgA | 2.1.1.182, 2.1.1.197, 2.5.1.134 | J | rRNA (adenine-N6,N6-)-dimethyltransferase activity | |
JHHLHNBC_00371 | 1.5e-294 | S | ABC transporter | |||
JHHLHNBC_00372 | 1.4e-175 | draG | O | ADP-ribosylglycohydrolase | ||
JHHLHNBC_00373 | 2e-107 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
JHHLHNBC_00374 | 2.6e-53 | |||||
JHHLHNBC_00375 | 4.8e-134 | XK27_06755 | S | Protein of unknown function (DUF975) | ||
JHHLHNBC_00376 | 8.9e-147 | M | Glycosyltransferase like family 2 | |||
JHHLHNBC_00377 | 2.2e-134 | glcR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_00378 | 4.3e-225 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
JHHLHNBC_00379 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
JHHLHNBC_00380 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
JHHLHNBC_00381 | 1.6e-104 | N | WxL domain surface cell wall-binding | |||
JHHLHNBC_00382 | 1.6e-111 | tdk | 2.7.1.21 | F | thymidine kinase | |
JHHLHNBC_00383 | 2.8e-175 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
JHHLHNBC_00384 | 1.8e-150 | 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 | |
JHHLHNBC_00385 | 1.2e-191 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
JHHLHNBC_00386 | 2.3e-221 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
JHHLHNBC_00387 | 5.7e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
JHHLHNBC_00388 | 4.9e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
JHHLHNBC_00389 | 5.6e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
JHHLHNBC_00390 | 6.3e-34 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
JHHLHNBC_00391 | 3.7e-246 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
JHHLHNBC_00392 | 5.9e-64 | |||||
JHHLHNBC_00393 | 3.7e-293 | clcA | P | chloride | ||
JHHLHNBC_00394 | 1.7e-60 | |||||
JHHLHNBC_00395 | 9.3e-31 | secG | U | Preprotein translocase | ||
JHHLHNBC_00396 | 1.2e-137 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
JHHLHNBC_00397 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
JHHLHNBC_00398 | 3.2e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
JHHLHNBC_00399 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
JHHLHNBC_00400 | 1.1e-104 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
JHHLHNBC_00401 | 1.3e-42 | |||||
JHHLHNBC_00402 | 9.3e-178 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
JHHLHNBC_00403 | 1.4e-53 | S | DsrE/DsrF-like family | |||
JHHLHNBC_00404 | 4.5e-253 | pbuO | S | permease | ||
JHHLHNBC_00405 | 7.5e-53 | S | Protein of unknown function (DUF1516) | |||
JHHLHNBC_00406 | 4.7e-193 | ldhD3 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
JHHLHNBC_00407 | 5e-79 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
JHHLHNBC_00408 | 6.2e-207 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
JHHLHNBC_00409 | 3e-27 | |||||
JHHLHNBC_00410 | 2.8e-204 | mccF | V | LD-carboxypeptidase | ||
JHHLHNBC_00411 | 8.2e-182 | I | PAP2 superfamily | |||
JHHLHNBC_00412 | 0.0 | nisT | V | ABC transporter | ||
JHHLHNBC_00413 | 7.7e-102 | |||||
JHHLHNBC_00414 | 6.6e-30 | higA | K | Helix-turn-helix XRE-family like proteins | ||
JHHLHNBC_00415 | 6.3e-34 | |||||
JHHLHNBC_00416 | 7.8e-98 | K | Protein of unknown function (DUF3955) | |||
JHHLHNBC_00417 | 2e-134 | |||||
JHHLHNBC_00418 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
JHHLHNBC_00419 | 9.3e-70 | |||||
JHHLHNBC_00422 | 1.1e-183 | yxaM | EGP | Major Facilitator Superfamily | ||
JHHLHNBC_00423 | 1e-55 | E | AAA domain | |||
JHHLHNBC_00424 | 4.2e-56 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
JHHLHNBC_00425 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
JHHLHNBC_00426 | 1.4e-250 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
JHHLHNBC_00427 | 8.1e-157 | K | Helix-turn-helix domain, rpiR family | |||
JHHLHNBC_00428 | 7.1e-200 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
JHHLHNBC_00429 | 2.4e-159 | 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 | |
JHHLHNBC_00430 | 0.0 | sacX | 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_00431 | 7.6e-219 | |||||
JHHLHNBC_00432 | 1.4e-251 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
JHHLHNBC_00433 | 4.6e-71 | rplI | J | Binds to the 23S rRNA | ||
JHHLHNBC_00434 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
JHHLHNBC_00436 | 4e-287 | glnP | P | ABC transporter permease | ||
JHHLHNBC_00449 | 2.7e-10 | |||||
JHHLHNBC_00450 | 3.1e-192 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
JHHLHNBC_00451 | 6.2e-161 | K | Transcriptional regulator | |||
JHHLHNBC_00452 | 4.3e-280 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
JHHLHNBC_00453 | 5.5e-194 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
JHHLHNBC_00454 | 6.2e-221 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
JHHLHNBC_00455 | 2.5e-50 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_00456 | 2.6e-245 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
JHHLHNBC_00457 | 9.7e-124 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
JHHLHNBC_00458 | 1.8e-173 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
JHHLHNBC_00459 | 6.5e-138 | lacT | K | PRD domain | ||
JHHLHNBC_00461 | 1.8e-133 | epsG | 2.4.1.293 | GT2 | M | Glycosyltransferase like family 2 |
JHHLHNBC_00462 | 5.9e-296 | 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 | |
JHHLHNBC_00463 | 0.0 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
JHHLHNBC_00464 | 1.9e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
JHHLHNBC_00465 | 5.8e-111 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
JHHLHNBC_00466 | 2.3e-157 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
JHHLHNBC_00467 | 1.3e-176 | 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) | |
JHHLHNBC_00468 | 2.3e-207 | E | glutamate:sodium symporter activity | |||
JHHLHNBC_00469 | 1.2e-260 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
JHHLHNBC_00470 | 3.8e-226 | Q | Imidazolonepropionase and related amidohydrolases | |||
JHHLHNBC_00471 | 2.3e-51 | nudA | S | ASCH domain | ||
JHHLHNBC_00472 | 1.5e-68 | |||||
JHHLHNBC_00473 | 3.9e-55 | 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 | ||
JHHLHNBC_00474 | 3.8e-177 | S | DUF218 domain | |||
JHHLHNBC_00475 | 4e-83 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
JHHLHNBC_00476 | 4.8e-265 | ywfO | S | HD domain protein | ||
JHHLHNBC_00477 | 3.3e-152 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
JHHLHNBC_00478 | 7e-80 | ywiB | S | Domain of unknown function (DUF1934) | ||
JHHLHNBC_00479 | 1.7e-107 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
JHHLHNBC_00480 | 5.2e-164 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
JHHLHNBC_00481 | 5e-78 | M | Glycosyl hydrolases family 25 | |||
JHHLHNBC_00482 | 5.7e-222 | M | Glycosyl hydrolases family 25 | |||
JHHLHNBC_00484 | 5.6e-239 | malE | G | Bacterial extracellular solute-binding protein | ||
JHHLHNBC_00485 | 2e-40 | |||||
JHHLHNBC_00486 | 9.3e-59 | glnQ | E | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00487 | 1e-276 | S | ABC-type transport system involved in multi-copper enzyme maturation permease component | |||
JHHLHNBC_00488 | 2.2e-151 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_00489 | 4.5e-99 | S | Putative adhesin | |||
JHHLHNBC_00490 | 8.5e-76 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
JHHLHNBC_00491 | 4.7e-52 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_00492 | 3.9e-168 | ssuA | P | NMT1-like family | ||
JHHLHNBC_00493 | 7.7e-296 | 6.2.1.3, 6.2.1.8 | IQ | AMP-binding enzyme C-terminal domain | ||
JHHLHNBC_00494 | 1.7e-229 | yfiQ | I | Acyltransferase family | ||
JHHLHNBC_00495 | 2.3e-122 | ssuB | P | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_00496 | 1.7e-145 | ssuC | U | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_00497 | 0.0 | |||||
JHHLHNBC_00498 | 7e-113 | V | ABC transporter | |||
JHHLHNBC_00499 | 1.4e-09 | S | Putative cell wall binding repeat | |||
JHHLHNBC_00500 | 5.1e-78 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
JHHLHNBC_00501 | 4.4e-228 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
JHHLHNBC_00502 | 1.3e-120 | |||||
JHHLHNBC_00503 | 1.4e-65 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_00504 | 6.4e-215 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
JHHLHNBC_00505 | 4.1e-192 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
JHHLHNBC_00506 | 8.8e-227 | iolF | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00507 | 2e-285 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
JHHLHNBC_00508 | 1.3e-56 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
JHHLHNBC_00509 | 5.4e-258 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
JHHLHNBC_00510 | 8e-168 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
JHHLHNBC_00511 | 0.0 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
JHHLHNBC_00512 | 8.5e-295 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5, 2.7.1.51 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
JHHLHNBC_00513 | 1.8e-232 | ywtG | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00514 | 6.4e-78 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
JHHLHNBC_00515 | 7.5e-146 | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | ||
JHHLHNBC_00516 | 1.1e-133 | fcsR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_00517 | 5e-136 | K | UbiC transcription regulator-associated domain protein | |||
JHHLHNBC_00518 | 1.2e-126 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
JHHLHNBC_00519 | 2.5e-261 | S | Putative peptidoglycan binding domain | |||
JHHLHNBC_00520 | 5.1e-119 | S | (CBS) domain | |||
JHHLHNBC_00521 | 3.6e-131 | yciB | M | ErfK YbiS YcfS YnhG | ||
JHHLHNBC_00522 | 5.6e-62 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
JHHLHNBC_00523 | 1.1e-37 | |||||
JHHLHNBC_00524 | 1.3e-218 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
JHHLHNBC_00525 | 5e-63 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
JHHLHNBC_00526 | 4.2e-254 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
JHHLHNBC_00527 | 8.9e-173 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
JHHLHNBC_00528 | 8.7e-165 | menA | 2.5.1.74 | M | UbiA prenyltransferase family | |
JHHLHNBC_00529 | 2.2e-196 | 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 | |
JHHLHNBC_00530 | 5.9e-85 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
JHHLHNBC_00531 | 4.7e-195 | nusA | K | Participates in both transcription termination and antitermination | ||
JHHLHNBC_00532 | 1.1e-46 | ylxR | K | Protein of unknown function (DUF448) | ||
JHHLHNBC_00533 | 1.2e-43 | ylxQ | J | ribosomal protein | ||
JHHLHNBC_00534 | 7.7e-149 | P | Belongs to the nlpA lipoprotein family | |||
JHHLHNBC_00535 | 2.4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
JHHLHNBC_00536 | 4.6e-31 | K | 'Cold-shock' DNA-binding domain | |||
JHHLHNBC_00537 | 4.9e-257 | yhdP | S | Transporter associated domain | ||
JHHLHNBC_00538 | 1.9e-144 | S | Alpha beta hydrolase | |||
JHHLHNBC_00539 | 7.8e-196 | I | Acyltransferase | |||
JHHLHNBC_00540 | 2.6e-261 | lmrB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00541 | 1.5e-83 | S | Domain of unknown function (DUF4811) | |||
JHHLHNBC_00542 | 9.4e-95 | maf | D | nucleoside-triphosphate diphosphatase activity | ||
JHHLHNBC_00543 | 1.6e-235 | 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 | ||
JHHLHNBC_00544 | 2.4e-188 | ydgH | S | MMPL family | ||
JHHLHNBC_00545 | 7.2e-181 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
JHHLHNBC_00546 | 4.7e-132 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
JHHLHNBC_00547 | 2.3e-102 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
JHHLHNBC_00548 | 2.5e-228 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
JHHLHNBC_00549 | 5.5e-136 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
JHHLHNBC_00551 | 4.3e-158 | S | CAAX protease self-immunity | |||
JHHLHNBC_00553 | 2.4e-116 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
JHHLHNBC_00554 | 4.8e-97 | dps | P | Belongs to the Dps family | ||
JHHLHNBC_00555 | 5.6e-33 | copZ | P | Heavy-metal-associated domain | ||
JHHLHNBC_00556 | 0.0 | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | ||
JHHLHNBC_00557 | 1.2e-214 | opuCA | E | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00558 | 4.7e-106 | opuCB | E | ABC transporter permease | ||
JHHLHNBC_00559 | 1.6e-174 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
JHHLHNBC_00560 | 1.9e-110 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_00562 | 2.5e-147 | S | Protein of unknown function (DUF3100) | |||
JHHLHNBC_00563 | 1.9e-69 | S | An automated process has identified a potential problem with this gene model | |||
JHHLHNBC_00564 | 8.1e-249 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
JHHLHNBC_00565 | 2.5e-122 | S | Sulfite exporter TauE/SafE | |||
JHHLHNBC_00566 | 2.7e-103 | K | Tetracycline repressor, C-terminal all-alpha domain | |||
JHHLHNBC_00567 | 9.1e-71 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
JHHLHNBC_00568 | 6.4e-38 | S | Transglycosylase associated protein | |||
JHHLHNBC_00569 | 1.5e-89 | S | Protein conserved in bacteria | |||
JHHLHNBC_00570 | 1.9e-29 | |||||
JHHLHNBC_00571 | 5.1e-61 | asp23 | S | Asp23 family, cell envelope-related function | ||
JHHLHNBC_00572 | 7.9e-65 | asp2 | S | Asp23 family, cell envelope-related function | ||
JHHLHNBC_00573 | 5e-127 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
JHHLHNBC_00574 | 6e-115 | S | Protein of unknown function (DUF969) | |||
JHHLHNBC_00575 | 6.7e-146 | S | Protein of unknown function (DUF979) | |||
JHHLHNBC_00576 | 2.9e-119 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
JHHLHNBC_00577 | 2.1e-106 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
JHHLHNBC_00579 | 1e-127 | cobQ | S | glutamine amidotransferase | ||
JHHLHNBC_00580 | 8.4e-66 | |||||
JHHLHNBC_00581 | 2e-132 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
JHHLHNBC_00582 | 2.4e-142 | noc | K | Belongs to the ParB family | ||
JHHLHNBC_00583 | 2.5e-138 | soj | D | Sporulation initiation inhibitor | ||
JHHLHNBC_00584 | 2e-155 | spo0J | K | Belongs to the ParB family | ||
JHHLHNBC_00585 | 1.3e-30 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
JHHLHNBC_00586 | 1.5e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
JHHLHNBC_00587 | 7.3e-141 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
JHHLHNBC_00588 | 4.6e-219 | ecsB | U | ABC transporter | ||
JHHLHNBC_00589 | 8.9e-133 | ecsA | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00590 | 2e-76 | hit | FG | histidine triad | ||
JHHLHNBC_00591 | 2.1e-58 | yhaH | S | YtxH-like protein | ||
JHHLHNBC_00592 | 1.6e-160 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
JHHLHNBC_00593 | 5.2e-181 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
JHHLHNBC_00594 | 4.6e-55 | yheA | S | Control of competence regulator ComK, YlbF/YmcA | ||
JHHLHNBC_00595 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
JHHLHNBC_00596 | 8.5e-148 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_00597 | 4e-75 | argR | K | Regulates arginine biosynthesis genes | ||
JHHLHNBC_00598 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
JHHLHNBC_00599 | 5.2e-231 | EK | Aminotransferase, class I | |||
JHHLHNBC_00600 | 5.8e-166 | K | LysR substrate binding domain | |||
JHHLHNBC_00601 | 3.6e-90 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
JHHLHNBC_00602 | 9.5e-152 | yitU | 3.1.3.104 | S | hydrolase | |
JHHLHNBC_00603 | 1.2e-126 | yjhF | G | Phosphoglycerate mutase family | ||
JHHLHNBC_00604 | 2.9e-117 | yoaK | S | Protein of unknown function (DUF1275) | ||
JHHLHNBC_00606 | 2.6e-54 | V | ABC transporter | |||
JHHLHNBC_00607 | 1.9e-08 | |||||
JHHLHNBC_00608 | 5.1e-28 | |||||
JHHLHNBC_00609 | 2.7e-43 | |||||
JHHLHNBC_00610 | 4.8e-12 | |||||
JHHLHNBC_00611 | 1.2e-58 | |||||
JHHLHNBC_00612 | 1.4e-142 | S | hydrolase | |||
JHHLHNBC_00613 | 1.4e-192 | yghZ | C | Aldo keto reductase family protein | ||
JHHLHNBC_00614 | 3.5e-42 | 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 | ||
JHHLHNBC_00615 | 8.4e-108 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
JHHLHNBC_00616 | 4.1e-99 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
JHHLHNBC_00617 | 1.3e-108 | draG | O | ADP-ribosylglycohydrolase | ||
JHHLHNBC_00618 | 2e-39 | draG | O | ADP-ribosylglycohydrolase | ||
JHHLHNBC_00619 | 5.8e-291 | S | ABC transporter | |||
JHHLHNBC_00620 | 9.1e-133 | 2.1.1.163, 2.1.1.201 | Q | Methyltransferase domain | ||
JHHLHNBC_00621 | 1.7e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
JHHLHNBC_00622 | 2.4e-153 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
JHHLHNBC_00623 | 1.3e-142 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
JHHLHNBC_00624 | 8.1e-182 | ansA | 3.5.1.1 | EJ | Asparaginase | |
JHHLHNBC_00625 | 9e-87 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
JHHLHNBC_00626 | 1.7e-108 | |||||
JHHLHNBC_00627 | 1.7e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
JHHLHNBC_00628 | 2.6e-152 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
JHHLHNBC_00629 | 1.1e-143 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
JHHLHNBC_00630 | 1.5e-180 | ansA | 3.5.1.1 | EJ | Asparaginase | |
JHHLHNBC_00631 | 7.3e-89 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
JHHLHNBC_00632 | 6.1e-123 | |||||
JHHLHNBC_00633 | 4.4e-83 | manR | 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |
JHHLHNBC_00634 | 1.4e-144 | tatD | L | hydrolase, TatD family | ||
JHHLHNBC_00635 | 1.6e-97 | 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 | |
JHHLHNBC_00636 | 4.1e-156 | 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 | |
JHHLHNBC_00637 | 6.2e-182 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
JHHLHNBC_00638 | 1.3e-157 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
JHHLHNBC_00639 | 7.4e-48 | yhaH | S | YtxH-like protein | ||
JHHLHNBC_00640 | 7.2e-74 | hit | FG | histidine triad | ||
JHHLHNBC_00641 | 4.9e-131 | ecsA | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00642 | 3.1e-223 | ecsB | U | ABC transporter | ||
JHHLHNBC_00643 | 1e-25 | K | acetyltransferase | |||
JHHLHNBC_00645 | 2.9e-90 | FNV0100 | F | NUDIX domain | ||
JHHLHNBC_00646 | 6.5e-140 | 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 | |
JHHLHNBC_00647 | 3.8e-128 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JHHLHNBC_00648 | 4.7e-280 | ytgP | S | Polysaccharide biosynthesis protein | ||
JHHLHNBC_00649 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_00650 | 7.2e-08 | T | SpoVT / AbrB like domain | |||
JHHLHNBC_00651 | 1.9e-194 | V | Beta-lactamase | |||
JHHLHNBC_00652 | 1.6e-137 | H | Protein of unknown function (DUF1698) | |||
JHHLHNBC_00653 | 1.7e-142 | puuD | S | peptidase C26 | ||
JHHLHNBC_00654 | 6.9e-256 | 6.3.1.2 | E | Glutamine synthetase N-terminal domain | ||
JHHLHNBC_00655 | 3.9e-220 | S | Amidohydrolase | |||
JHHLHNBC_00656 | 3.4e-247 | E | Amino acid permease | |||
JHHLHNBC_00657 | 4.7e-73 | K | transcriptional regulator, MerR family | |||
JHHLHNBC_00658 | 1.7e-162 | morA2 | S | reductase | ||
JHHLHNBC_00659 | 8.8e-195 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
JHHLHNBC_00660 | 8.4e-57 | hxlR | K | Transcriptional regulator, HxlR family | ||
JHHLHNBC_00661 | 8e-129 | S | membrane transporter protein | |||
JHHLHNBC_00662 | 3.2e-130 | XK27_12140 | V | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_00663 | 1.9e-292 | S | Psort location CytoplasmicMembrane, score | |||
JHHLHNBC_00666 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
JHHLHNBC_00667 | 4.2e-308 | 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 | ||
JHHLHNBC_00668 | 6.5e-184 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
JHHLHNBC_00669 | 2.1e-243 | els | S | Sterol carrier protein domain | ||
JHHLHNBC_00670 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
JHHLHNBC_00671 | 1.4e-116 | S | Repeat protein | |||
JHHLHNBC_00672 | 1.3e-122 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
JHHLHNBC_00673 | 7.4e-219 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
JHHLHNBC_00674 | 1.7e-43 | trxC | O | Belongs to the thioredoxin family | ||
JHHLHNBC_00675 | 6.6e-134 | thrE | S | Putative threonine/serine exporter | ||
JHHLHNBC_00676 | 3.5e-74 | S | Threonine/Serine exporter, ThrE | |||
JHHLHNBC_00677 | 4.4e-214 | livJ | E | Receptor family ligand binding region | ||
JHHLHNBC_00678 | 6.7e-151 | livH | U | Branched-chain amino acid transport system / permease component | ||
JHHLHNBC_00679 | 1.7e-120 | livM | E | Branched-chain amino acid transport system / permease component | ||
JHHLHNBC_00680 | 2.1e-140 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
JHHLHNBC_00681 | 1.1e-124 | livF | E | ABC transporter | ||
JHHLHNBC_00682 | 4.7e-290 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
JHHLHNBC_00683 | 3.9e-116 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
JHHLHNBC_00684 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
JHHLHNBC_00685 | 2.1e-49 | yajC | U | Preprotein translocase | ||
JHHLHNBC_00686 | 1e-228 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
JHHLHNBC_00687 | 0.0 | 2.1.1.72 | V | Eco57I restriction-modification methylase | ||
JHHLHNBC_00688 | 1.8e-190 | L | Belongs to the 'phage' integrase family | |||
JHHLHNBC_00689 | 1.2e-196 | V | site-specific DNA-methyltransferase (adenine-specific) activity | |||
JHHLHNBC_00690 | 3.6e-188 | cggR | K | Putative sugar-binding domain | ||
JHHLHNBC_00691 | 7.1e-245 | 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 | |
JHHLHNBC_00692 | 5.3e-119 | |||||
JHHLHNBC_00693 | 8.7e-122 | K | response regulator | |||
JHHLHNBC_00694 | 2.5e-217 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_00695 | 3.9e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
JHHLHNBC_00696 | 1.7e-79 | 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 | ||
JHHLHNBC_00697 | 7.1e-289 | 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 | |
JHHLHNBC_00698 | 6.3e-134 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
JHHLHNBC_00699 | 1.2e-165 | yvgN | C | Aldo keto reductase | ||
JHHLHNBC_00700 | 1.8e-142 | iolR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_00701 | 1.2e-266 | iolT | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00702 | 2.2e-279 | iolA | 1.2.1.18, 1.2.1.27 | C | Belongs to the aldehyde dehydrogenase family | |
JHHLHNBC_00703 | 1.3e-156 | iolB | 5.3.1.30 | G | Involved in the isomerization of 5-deoxy-glucuronate (5DG) to 5-dehydro-2-deoxy-D-gluconate (DKG or 2-deoxy-5-keto-D- gluconate) | |
JHHLHNBC_00704 | 1.3e-176 | iolC | 2.7.1.92 | H | Catalyzes the phosphorylation of 5-dehydro-2-deoxy-D- gluconate (2-deoxy-5-keto-D-gluconate or DKG) to 6-phospho-5- dehydro-2-deoxy-D-gluconate (DKGP) | |
JHHLHNBC_00705 | 0.0 | iolD | 3.7.1.22 | E | Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) | |
JHHLHNBC_00706 | 3.1e-195 | iolG2 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
JHHLHNBC_00707 | 2.8e-173 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
JHHLHNBC_00708 | 9.6e-158 | iolJ | 4.1.2.13, 4.1.2.29 | G | aldolase | |
JHHLHNBC_00709 | 8.6e-66 | iolK | S | Tautomerase enzyme | ||
JHHLHNBC_00710 | 5e-146 | iolI | 5.3.99.11 | G | Xylose isomerase-like TIM barrel | |
JHHLHNBC_00711 | 5e-167 | iolH | G | Xylose isomerase-like TIM barrel | ||
JHHLHNBC_00712 | 4e-145 | gntR | K | rpiR family | ||
JHHLHNBC_00713 | 3.7e-246 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
JHHLHNBC_00714 | 2e-291 | clcA | P | chloride | ||
JHHLHNBC_00715 | 1.8e-57 | |||||
JHHLHNBC_00716 | 1.4e-31 | secG | U | Preprotein translocase | ||
JHHLHNBC_00717 | 4.9e-139 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
JHHLHNBC_00718 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
JHHLHNBC_00719 | 9.4e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
JHHLHNBC_00720 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
JHHLHNBC_00721 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
JHHLHNBC_00722 | 1.9e-113 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
JHHLHNBC_00724 | 2.7e-25 | ydcG | K | Transcriptional | ||
JHHLHNBC_00725 | 2.6e-233 | YSH1 | S | Metallo-beta-lactamase superfamily | ||
JHHLHNBC_00726 | 2.4e-217 | V | Beta-lactamase | |||
JHHLHNBC_00727 | 1.3e-151 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
JHHLHNBC_00728 | 1e-162 | V | Beta-lactamase | |||
JHHLHNBC_00729 | 5.3e-80 | perR | P | Belongs to the Fur family | ||
JHHLHNBC_00730 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
JHHLHNBC_00731 | 5.1e-44 | ykuJ | S | Protein of unknown function (DUF1797) | ||
JHHLHNBC_00732 | 4.3e-64 | yugI | 5.3.1.9 | J | general stress protein | |
JHHLHNBC_00733 | 5.6e-26 | |||||
JHHLHNBC_00734 | 1.8e-81 | gpm5 | 3.1.3.3, 5.4.2.11 | G | Phosphoglycerate mutase family | |
JHHLHNBC_00735 | 5e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
JHHLHNBC_00736 | 8.2e-37 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
JHHLHNBC_00737 | 7.1e-127 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
JHHLHNBC_00738 | 1.7e-189 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
JHHLHNBC_00739 | 2.7e-169 | yicL | EG | EamA-like transporter family | ||
JHHLHNBC_00740 | 4e-301 | |||||
JHHLHNBC_00741 | 2.7e-143 | CcmA5 | V | ABC transporter | ||
JHHLHNBC_00742 | 6.2e-78 | S | ECF-type riboflavin transporter, S component | |||
JHHLHNBC_00743 | 1.2e-146 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
JHHLHNBC_00744 | 1.7e-162 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
JHHLHNBC_00745 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
JHHLHNBC_00746 | 0.0 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00747 | 0.0 | V | ABC transporter | |||
JHHLHNBC_00748 | 4.7e-219 | oxlT | P | Major Facilitator Superfamily | ||
JHHLHNBC_00749 | 3.2e-127 | treR | K | UTRA | ||
JHHLHNBC_00750 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
JHHLHNBC_00751 | 0.0 | treB | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_00752 | 6.9e-213 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
JHHLHNBC_00753 | 1.2e-269 | yfnA | E | Amino Acid | ||
JHHLHNBC_00754 | 1.6e-171 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
JHHLHNBC_00755 | 5.5e-127 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_00757 | 1.3e-96 | 2.3.1.128, 5.2.1.8 | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_00758 | 1.7e-285 | arlS | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_00759 | 7.9e-123 | K | response regulator | |||
JHHLHNBC_00760 | 1.8e-270 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
JHHLHNBC_00761 | 7.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
JHHLHNBC_00762 | 6.3e-210 | ylbM | S | Belongs to the UPF0348 family | ||
JHHLHNBC_00763 | 1.9e-135 | yqeM | Q | Methyltransferase | ||
JHHLHNBC_00764 | 1.4e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
JHHLHNBC_00765 | 3.9e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
JHHLHNBC_00766 | 9.7e-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) | |
JHHLHNBC_00767 | 1.1e-47 | yhbY | J | RNA-binding protein | ||
JHHLHNBC_00768 | 1.1e-217 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
JHHLHNBC_00769 | 3.8e-96 | yqeG | S | HAD phosphatase, family IIIA | ||
JHHLHNBC_00770 | 5.4e-172 | ykcA | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
JHHLHNBC_00771 | 2.8e-190 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
JHHLHNBC_00772 | 1.7e-119 | mhqD | S | Dienelactone hydrolase family | ||
JHHLHNBC_00773 | 2.4e-178 | 3.5.1.10 | C | Alcohol dehydrogenase GroES-like domain | ||
JHHLHNBC_00774 | 3.6e-81 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
JHHLHNBC_00775 | 1.3e-35 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
JHHLHNBC_00776 | 3.2e-268 | ytgP | S | Polysaccharide biosynthesis protein | ||
JHHLHNBC_00777 | 6.9e-130 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JHHLHNBC_00778 | 2.1e-34 | yhcC | S | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | ||
JHHLHNBC_00779 | 5e-140 | 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 | |
JHHLHNBC_00780 | 1.7e-95 | FNV0100 | F | NUDIX domain | ||
JHHLHNBC_00781 | 8.5e-148 | P | Belongs to the nlpA lipoprotein family | |||
JHHLHNBC_00782 | 1.4e-81 | ccl | S | QueT transporter | ||
JHHLHNBC_00783 | 4.1e-130 | E | lipolytic protein G-D-S-L family | |||
JHHLHNBC_00784 | 9.8e-129 | epsB | M | biosynthesis protein | ||
JHHLHNBC_00785 | 9.2e-109 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
JHHLHNBC_00786 | 1.4e-198 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
JHHLHNBC_00787 | 2.7e-210 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
JHHLHNBC_00788 | 4e-79 | M | Core-2/I-Branching enzyme | |||
JHHLHNBC_00789 | 9.3e-71 | 1.1.1.133 | S | Glycosyltransferase like family 2 | ||
JHHLHNBC_00790 | 2.8e-62 | GT2,GT4 | M | Glycosyltransferase GT-D fold | ||
JHHLHNBC_00791 | 2.5e-64 | cps1D | M | Domain of unknown function (DUF4422) | ||
JHHLHNBC_00792 | 4e-25 | |||||
JHHLHNBC_00793 | 5.8e-65 | glfT1 | 1.1.1.133 | S | Glycosyltransferase like family 2 | |
JHHLHNBC_00794 | 2.6e-115 | vraR | K | helix_turn_helix, Lux Regulon | ||
JHHLHNBC_00795 | 5.8e-54 | yneR | S | Belongs to the HesB IscA family | ||
JHHLHNBC_00796 | 0.0 | S | Bacterial membrane protein YfhO | |||
JHHLHNBC_00797 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
JHHLHNBC_00798 | 2.5e-121 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
JHHLHNBC_00799 | 4e-40 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
JHHLHNBC_00800 | 3.7e-179 | glk | 2.7.1.2 | G | Glucokinase | |
JHHLHNBC_00801 | 1.7e-72 | yqhL | P | Rhodanese-like protein | ||
JHHLHNBC_00802 | 4.4e-25 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
JHHLHNBC_00803 | 5.4e-178 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
JHHLHNBC_00804 | 2.2e-240 | ynbB | 4.4.1.1 | P | aluminum resistance | |
JHHLHNBC_00805 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
JHHLHNBC_00806 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
JHHLHNBC_00807 | 9.2e-181 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
JHHLHNBC_00809 | 8.5e-81 | divIVA | D | DivIVA protein | ||
JHHLHNBC_00810 | 1.9e-112 | ylmH | S | S4 domain protein | ||
JHHLHNBC_00811 | 3.1e-49 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
JHHLHNBC_00812 | 1.5e-22 | 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 | ||
JHHLHNBC_00813 | 3.7e-117 | radC | L | DNA repair protein | ||
JHHLHNBC_00814 | 1.8e-116 | S | Haloacid dehalogenase-like hydrolase | |||
JHHLHNBC_00815 | 1.9e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
JHHLHNBC_00816 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
JHHLHNBC_00817 | 6.8e-27 | |||||
JHHLHNBC_00818 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
JHHLHNBC_00819 | 4.2e-27 | ykuJ | S | Protein of unknown function (DUF1797) | ||
JHHLHNBC_00820 | 3.1e-28 | |||||
JHHLHNBC_00821 | 9.3e-14 | S | Addiction module antitoxin, RelB DinJ family | |||
JHHLHNBC_00822 | 3.4e-96 | araR | K | Transcriptional regulator | ||
JHHLHNBC_00823 | 4.4e-07 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_00824 | 1.6e-223 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
JHHLHNBC_00825 | 3.2e-08 | L | IS66 Orf2 like protein | |||
JHHLHNBC_00826 | 0.0 | CP_0954 | 4.2.2.1 | PL8 | N | Polysaccharide lyase family 8, N terminal alpha-helical domain |
JHHLHNBC_00827 | 2.3e-209 | yesR | 3.2.1.172 | GH105 | S | Glycosyl Hydrolase Family 88 |
JHHLHNBC_00828 | 7.7e-269 | gph | G | MFS/sugar transport protein | ||
JHHLHNBC_00829 | 3.6e-38 | |||||
JHHLHNBC_00830 | 3.9e-145 | G | Xylose isomerase-like TIM barrel | |||
JHHLHNBC_00831 | 7.4e-152 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
JHHLHNBC_00832 | 2.4e-166 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
JHHLHNBC_00833 | 3.7e-148 | Z012_03480 | S | Psort location Cytoplasmic, score | ||
JHHLHNBC_00834 | 8.2e-137 | K | Bacterial transcriptional regulator | |||
JHHLHNBC_00835 | 1.2e-126 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
JHHLHNBC_00836 | 9.4e-233 | ugl | 3.2.1.180 | GH88 | S | Glycosyl Hydrolase Family 88 |
JHHLHNBC_00837 | 7.1e-89 | agaV | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_00838 | 2.8e-143 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_00839 | 3.3e-144 | agaD | G | PTS system mannose/fructose/sorbose family IID component | ||
JHHLHNBC_00840 | 2.1e-82 | G | PTS system fructose IIA component | |||
JHHLHNBC_00842 | 0.0 | S | Heparinase II/III N-terminus | |||
JHHLHNBC_00843 | 2.5e-170 | |||||
JHHLHNBC_00844 | 0.0 | plyA3 | M | Right handed beta helix region | ||
JHHLHNBC_00845 | 5.1e-81 | guaD | 3.5.4.12, 3.5.4.3, 3.5.4.33 | FJ | MafB19-like deaminase | |
JHHLHNBC_00846 | 6.7e-170 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
JHHLHNBC_00847 | 1.2e-224 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
JHHLHNBC_00848 | 3.7e-65 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
JHHLHNBC_00849 | 1.2e-152 | F | DNA/RNA non-specific endonuclease | |||
JHHLHNBC_00850 | 1.7e-47 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
JHHLHNBC_00851 | 4e-123 | |||||
JHHLHNBC_00853 | 2.1e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
JHHLHNBC_00854 | 3.7e-57 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_00855 | 2.6e-38 | 2.7.1.194, 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_00856 | 2.2e-219 | S | PTS system sugar-specific permease component | |||
JHHLHNBC_00857 | 1.1e-53 | 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 | ||
JHHLHNBC_00858 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
JHHLHNBC_00859 | 3.2e-101 | feoA | P | FeoA | ||
JHHLHNBC_00860 | 1.9e-122 | E | lipolytic protein G-D-S-L family | |||
JHHLHNBC_00861 | 3.5e-88 | E | AAA domain | |||
JHHLHNBC_00862 | 4.9e-284 | pipD | E | Dipeptidase | ||
JHHLHNBC_00863 | 4.4e-214 | yttB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00864 | 1.2e-17 | |||||
JHHLHNBC_00865 | 7.5e-285 | pipD | E | Dipeptidase | ||
JHHLHNBC_00866 | 3.3e-193 | yttB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00867 | 1.2e-17 | |||||
JHHLHNBC_00868 | 1.4e-153 | 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 | ||
JHHLHNBC_00869 | 1.8e-108 | |||||
JHHLHNBC_00870 | 1.8e-153 | 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 | ||
JHHLHNBC_00871 | 1.4e-116 | |||||
JHHLHNBC_00872 | 2.3e-73 | S | Protein of unknown function (DUF3290) | |||
JHHLHNBC_00873 | 1e-116 | yviA | S | Protein of unknown function (DUF421) | ||
JHHLHNBC_00874 | 1.1e-161 | S | Alpha beta hydrolase | |||
JHHLHNBC_00875 | 9.9e-57 | |||||
JHHLHNBC_00876 | 0.0 | clpB | 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 | ||
JHHLHNBC_00877 | 1.3e-46 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
JHHLHNBC_00878 | 1.1e-121 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
JHHLHNBC_00879 | 1.5e-183 | 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 | |
JHHLHNBC_00880 | 7.7e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
JHHLHNBC_00881 | 5.6e-94 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
JHHLHNBC_00883 | 3.1e-68 | yodB | K | Transcriptional regulator, HxlR family | ||
JHHLHNBC_00884 | 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 | |
JHHLHNBC_00885 | 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 | |
JHHLHNBC_00886 | 2.8e-44 | L | PFAM IS66 Orf2 family protein | |||
JHHLHNBC_00887 | 1.6e-67 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_00888 | 9.3e-112 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
JHHLHNBC_00889 | 1.8e-08 | |||||
JHHLHNBC_00890 | 5.6e-85 | zur | P | Belongs to the Fur family | ||
JHHLHNBC_00892 | 3.4e-172 | |||||
JHHLHNBC_00893 | 1.8e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_00894 | 3.4e-149 | glnH | ET | ABC transporter substrate-binding protein | ||
JHHLHNBC_00895 | 7.9e-109 | gluC | P | ABC transporter permease | ||
JHHLHNBC_00896 | 1.1e-110 | glnP | P | ABC transporter permease | ||
JHHLHNBC_00897 | 5.4e-175 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
JHHLHNBC_00898 | 1e-257 | wcaJ | M | Bacterial sugar transferase | ||
JHHLHNBC_00899 | 4.1e-215 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
JHHLHNBC_00900 | 1.7e-81 | ynhH | S | NusG domain II | ||
JHHLHNBC_00901 | 8.5e-91 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
JHHLHNBC_00903 | 1.6e-222 | yceI | G | Sugar (and other) transporter | ||
JHHLHNBC_00904 | 3.1e-90 | |||||
JHHLHNBC_00905 | 6.5e-156 | K | acetyltransferase | |||
JHHLHNBC_00906 | 9.8e-225 | mdtG | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00907 | 2.3e-98 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
JHHLHNBC_00908 | 1.8e-187 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
JHHLHNBC_00909 | 3.6e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_00910 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00911 | 8.9e-69 | S | Domain of unknown function (DUF4918) | |||
JHHLHNBC_00913 | 3e-56 | |||||
JHHLHNBC_00914 | 1.1e-256 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
JHHLHNBC_00915 | 2.3e-40 | yozE | S | Belongs to the UPF0346 family | ||
JHHLHNBC_00916 | 1.5e-85 | msrA | 1.8.4.11, 1.8.4.12 | C | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
JHHLHNBC_00917 | 9e-113 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
JHHLHNBC_00918 | 7.8e-157 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
JHHLHNBC_00919 | 2.9e-125 | ykcC | GT2 | M | Glycosyl transferase family 2 | |
JHHLHNBC_00920 | 1.5e-219 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
JHHLHNBC_00921 | 9.7e-212 | mvaA | 1.1.1.34, 1.1.1.88 | C | Belongs to the HMG-CoA reductase family | |
JHHLHNBC_00922 | 5e-210 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
JHHLHNBC_00923 | 3.3e-49 | |||||
JHHLHNBC_00924 | 3e-161 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
JHHLHNBC_00925 | 1.8e-101 | V | Restriction endonuclease | |||
JHHLHNBC_00926 | 0.0 | O | Belongs to the peptidase S8 family | |||
JHHLHNBC_00927 | 1.7e-44 | |||||
JHHLHNBC_00928 | 1.8e-159 | bglK_1 | GK | ROK family | ||
JHHLHNBC_00929 | 1.4e-181 | aspG | 3.4.19.5, 3.5.1.1, 3.5.1.26 | E | Asparaginase | |
JHHLHNBC_00930 | 5.2e-256 | 3.5.1.18 | E | Peptidase family M20/M25/M40 | ||
JHHLHNBC_00931 | 2.2e-131 | ymfC | K | UTRA | ||
JHHLHNBC_00932 | 5.3e-215 | uhpT | EGP | Major facilitator Superfamily | ||
JHHLHNBC_00933 | 5.4e-208 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
JHHLHNBC_00934 | 2.7e-97 | S | Domain of unknown function (DUF4428) | |||
JHHLHNBC_00935 | 1.5e-288 | xylB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
JHHLHNBC_00936 | 1.2e-204 | C | Zinc-binding dehydrogenase | |||
JHHLHNBC_00937 | 1.3e-151 | manZ | G | PTS system mannose/fructose/sorbose family IID component | ||
JHHLHNBC_00938 | 3.7e-137 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_00939 | 8.5e-84 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_00940 | 8.5e-288 | yloV | S | DAK2 domain fusion protein YloV | ||
JHHLHNBC_00941 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
JHHLHNBC_00942 | 5.1e-190 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
JHHLHNBC_00943 | 3.4e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
JHHLHNBC_00944 | 1.5e-194 | oppD | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_00945 | 1.7e-148 | dprA | LU | DNA protecting protein DprA | ||
JHHLHNBC_00946 | 9.2e-141 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
JHHLHNBC_00947 | 1.4e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
JHHLHNBC_00948 | 5.9e-38 | S | Domain of unknown function (DUF4918) | |||
JHHLHNBC_00949 | 1.7e-194 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
JHHLHNBC_00950 | 6.4e-31 | yaaA | S | S4 domain protein YaaA | ||
JHHLHNBC_00951 | 6.9e-201 | 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 | ||
JHHLHNBC_00952 | 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 | |
JHHLHNBC_00953 | 8.5e-151 | mreC | M | Involved in formation and maintenance of cell shape | ||
JHHLHNBC_00954 | 4.7e-83 | mreD | M | rod shape-determining protein MreD | ||
JHHLHNBC_00955 | 2e-112 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
JHHLHNBC_00956 | 1.1e-141 | minD | D | Belongs to the ParA family | ||
JHHLHNBC_00957 | 4.7e-109 | artQ | P | ABC transporter permease | ||
JHHLHNBC_00958 | 6.4e-111 | glnQ | 3.6.3.21 | E | ABC transporter | |
JHHLHNBC_00959 | 9.5e-152 | aatB | ET | ABC transporter substrate-binding protein | ||
JHHLHNBC_00960 | 4.2e-162 | ypuA | S | Protein of unknown function (DUF1002) | ||
JHHLHNBC_00962 | 3.8e-98 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
JHHLHNBC_00963 | 4.4e-169 | |||||
JHHLHNBC_00964 | 2.8e-17 | |||||
JHHLHNBC_00965 | 2.2e-128 | cobB | K | Sir2 family | ||
JHHLHNBC_00966 | 9e-107 | yiiE | S | Protein of unknown function (DUF1211) | ||
JHHLHNBC_00967 | 1.5e-169 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
JHHLHNBC_00968 | 3.8e-92 | 3.6.1.55 | F | NUDIX domain | ||
JHHLHNBC_00969 | 1.9e-152 | yunF | F | Protein of unknown function DUF72 | ||
JHHLHNBC_00970 | 6.9e-150 | manN | G | system, mannose fructose sorbose family IID component | ||
JHHLHNBC_00971 | 4.6e-118 | |||||
JHHLHNBC_00972 | 2.2e-123 | |||||
JHHLHNBC_00973 | 1.1e-118 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_00974 | 4.8e-79 | |||||
JHHLHNBC_00975 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_00976 | 9.2e-192 | ypdE | E | M42 glutamyl aminopeptidase | ||
JHHLHNBC_00977 | 3.8e-48 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
JHHLHNBC_00978 | 1.8e-59 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_00979 | 3.1e-253 | 2.7.1.207 | U | 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 | ||
JHHLHNBC_00980 | 4.1e-203 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
JHHLHNBC_00981 | 1.5e-233 | 4.4.1.8 | E | Aminotransferase, class I | ||
JHHLHNBC_00982 | 2.2e-219 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
JHHLHNBC_00983 | 0.0 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
JHHLHNBC_00984 | 3.4e-241 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
JHHLHNBC_00985 | 2.7e-135 | cad | S | FMN_bind | ||
JHHLHNBC_00986 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
JHHLHNBC_00987 | 2.8e-114 | S | NADPH-dependent FMN reductase | |||
JHHLHNBC_00988 | 6.5e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
JHHLHNBC_00989 | 8.3e-190 | 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 | ||
JHHLHNBC_00990 | 3.9e-292 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
JHHLHNBC_00991 | 3.1e-230 | 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 | |
JHHLHNBC_00992 | 1.3e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
JHHLHNBC_00993 | 1.7e-42 | ycfI | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_00994 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
JHHLHNBC_00995 | 9.7e-46 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
JHHLHNBC_00996 | 7.9e-304 | 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 | ||
JHHLHNBC_00997 | 8.5e-246 | hlyX | S | Transporter associated domain | ||
JHHLHNBC_00998 | 8.3e-181 | yueF | S | AI-2E family transporter | ||
JHHLHNBC_00999 | 1.9e-74 | S | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_01000 | 5.2e-95 | |||||
JHHLHNBC_01001 | 8.9e-104 | ygaC | J | Belongs to the UPF0374 family | ||
JHHLHNBC_01002 | 1.1e-141 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
JHHLHNBC_01003 | 7e-289 | frvR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_01004 | 1.1e-57 | |||||
JHHLHNBC_01005 | 1.2e-258 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
JHHLHNBC_01006 | 5.7e-80 | F | Nucleoside 2-deoxyribosyltransferase | |||
JHHLHNBC_01007 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_01008 | 4.9e-221 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
JHHLHNBC_01009 | 2.8e-214 | mvaA | 1.1.1.34, 1.1.1.88 | C | Belongs to the HMG-CoA reductase family | |
JHHLHNBC_01010 | 5.5e-209 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
JHHLHNBC_01011 | 4.7e-48 | |||||
JHHLHNBC_01012 | 3.7e-159 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
JHHLHNBC_01013 | 1.1e-101 | V | Restriction endonuclease | |||
JHHLHNBC_01014 | 3.5e-154 | 5.1.3.3 | G | converts alpha-aldose to the beta-anomer | ||
JHHLHNBC_01015 | 7.2e-214 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
JHHLHNBC_01016 | 5.2e-102 | S | ECF transporter, substrate-specific component | |||
JHHLHNBC_01017 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
JHHLHNBC_01018 | 4.3e-46 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
JHHLHNBC_01019 | 3.6e-304 | 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 | ||
JHHLHNBC_01020 | 1.4e-139 | hlyX | S | Transporter associated domain | ||
JHHLHNBC_01021 | 3.6e-140 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
JHHLHNBC_01022 | 2.8e-137 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
JHHLHNBC_01024 | 4e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
JHHLHNBC_01025 | 5.9e-129 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
JHHLHNBC_01026 | 3.4e-155 | 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 | ||
JHHLHNBC_01027 | 1.3e-85 | |||||
JHHLHNBC_01028 | 8.7e-92 | S | MucBP domain | |||
JHHLHNBC_01029 | 2.9e-119 | ywnB | S | NAD(P)H-binding | ||
JHHLHNBC_01031 | 4.9e-125 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
JHHLHNBC_01032 | 1.9e-175 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
JHHLHNBC_01033 | 7e-124 | S | Domain of unknown function (DUF4867) | |||
JHHLHNBC_01034 | 1e-187 | V | peptidase activity | |||
JHHLHNBC_01035 | 7.4e-130 | S | membrane transporter protein | |||
JHHLHNBC_01036 | 2.3e-81 | |||||
JHHLHNBC_01037 | 6.5e-75 | G | PTS system fructose IIA component | |||
JHHLHNBC_01038 | 2.1e-135 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_01039 | 2.8e-127 | agaC | G | PTS system sorbose-specific iic component | ||
JHHLHNBC_01040 | 1.5e-86 | agaB | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_01041 | 1.2e-191 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
JHHLHNBC_01042 | 6.3e-125 | yihT | 4.1.2.40, 4.1.2.57 | G | Belongs to the aldolase LacD family | |
JHHLHNBC_01043 | 2.6e-171 | yqhA | G | Aldose 1-epimerase | ||
JHHLHNBC_01044 | 1.9e-124 | T | LytTr DNA-binding domain | |||
JHHLHNBC_01045 | 4.3e-169 | T | GHKL domain | |||
JHHLHNBC_01046 | 0.0 | V | ABC transporter | |||
JHHLHNBC_01047 | 0.0 | V | ABC transporter | |||
JHHLHNBC_01048 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
JHHLHNBC_01050 | 1.2e-211 | ysaA | V | RDD family | ||
JHHLHNBC_01051 | 2.9e-151 | purR | 2.4.2.7 | F | pur operon repressor | |
JHHLHNBC_01052 | 5.9e-120 | ybbL | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01053 | 1.7e-118 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
JHHLHNBC_01054 | 1.3e-159 | czcD | P | cation diffusion facilitator family transporter | ||
JHHLHNBC_01055 | 3.3e-166 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
JHHLHNBC_01056 | 1.9e-37 | veg | S | Biofilm formation stimulator VEG | ||
JHHLHNBC_01057 | 5e-79 | |||||
JHHLHNBC_01058 | 1.5e-149 | T | Calcineurin-like phosphoesterase superfamily domain | |||
JHHLHNBC_01059 | 1e-96 | |||||
JHHLHNBC_01060 | 9.7e-158 | |||||
JHHLHNBC_01061 | 8.1e-157 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_01062 | 7.1e-223 | |||||
JHHLHNBC_01063 | 9.6e-195 | |||||
JHHLHNBC_01064 | 5.1e-122 | 1.5.1.40 | S | Rossmann-like domain | ||
JHHLHNBC_01065 | 1.9e-192 | XK27_00915 | C | Luciferase-like monooxygenase | ||
JHHLHNBC_01066 | 1.2e-97 | yacP | S | YacP-like NYN domain | ||
JHHLHNBC_01067 | 1.2e-143 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
JHHLHNBC_01068 | 1.8e-72 | 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) | ||
JHHLHNBC_01069 | 2.9e-273 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_01070 | 4.9e-162 | K | sequence-specific DNA binding | |||
JHHLHNBC_01071 | 4.3e-245 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
JHHLHNBC_01072 | 2.8e-105 | |||||
JHHLHNBC_01074 | 3.3e-259 | 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) | |
JHHLHNBC_01075 | 1.8e-156 | ykuT | M | mechanosensitive ion channel | ||
JHHLHNBC_01076 | 9.3e-156 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
JHHLHNBC_01077 | 3e-84 | ykuL | S | CBS domain | ||
JHHLHNBC_01078 | 5.2e-133 | gla | U | Major intrinsic protein | ||
JHHLHNBC_01079 | 6.9e-95 | S | Phosphoesterase | |||
JHHLHNBC_01080 | 5.3e-278 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
JHHLHNBC_01081 | 2.2e-61 | copB | 3.6.3.4 | P | P-type ATPase | |
JHHLHNBC_01082 | 1.6e-106 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
JHHLHNBC_01083 | 4.5e-166 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
JHHLHNBC_01084 | 1.9e-83 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
JHHLHNBC_01085 | 5.1e-131 | K | Helix-turn-helix domain, rpiR family | |||
JHHLHNBC_01087 | 1.3e-298 | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
JHHLHNBC_01088 | 5.8e-274 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain | |
JHHLHNBC_01089 | 9.5e-49 | |||||
JHHLHNBC_01090 | 7.6e-126 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
JHHLHNBC_01091 | 8.3e-61 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
JHHLHNBC_01092 | 2.6e-186 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
JHHLHNBC_01093 | 1.5e-272 | E | Amino acid permease | |||
JHHLHNBC_01094 | 2.7e-149 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
JHHLHNBC_01095 | 1.4e-102 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
JHHLHNBC_01096 | 6e-149 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
JHHLHNBC_01097 | 1.9e-81 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
JHHLHNBC_01098 | 4.5e-126 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
JHHLHNBC_01099 | 1.2e-100 | yebC | K | Transcriptional regulatory protein | ||
JHHLHNBC_01100 | 1.9e-150 | comGA | NU | Type II IV secretion system protein | ||
JHHLHNBC_01101 | 2.8e-163 | comGB | NU | type II secretion system | ||
JHHLHNBC_01102 | 2.5e-47 | |||||
JHHLHNBC_01104 | 1.8e-33 | |||||
JHHLHNBC_01105 | 1.5e-56 | |||||
JHHLHNBC_01106 | 4.4e-20 | |||||
JHHLHNBC_01107 | 2.3e-187 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
JHHLHNBC_01109 | 3.8e-73 | |||||
JHHLHNBC_01110 | 1.8e-243 | cycA | E | Amino acid permease | ||
JHHLHNBC_01111 | 4.8e-145 | arbV | 2.3.1.51 | I | Phosphate acyltransferases | |
JHHLHNBC_01112 | 9.6e-163 | arbx | M | Glycosyl transferase family 8 | ||
JHHLHNBC_01113 | 3.6e-182 | arbY | M | family 8 | ||
JHHLHNBC_01114 | 1.6e-165 | arbZ | I | Phosphate acyltransferases | ||
JHHLHNBC_01115 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
JHHLHNBC_01118 | 3.2e-209 | sip | L | Belongs to the 'phage' integrase family | ||
JHHLHNBC_01119 | 1.5e-08 | K | sequence-specific DNA binding | |||
JHHLHNBC_01120 | 7.8e-13 | |||||
JHHLHNBC_01121 | 1.5e-30 | |||||
JHHLHNBC_01122 | 1.1e-12 | |||||
JHHLHNBC_01123 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
JHHLHNBC_01124 | 2.3e-179 | ccpA | K | catabolite control protein A | ||
JHHLHNBC_01125 | 7.5e-216 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
JHHLHNBC_01126 | 5e-93 | niaR | S | 3H domain | ||
JHHLHNBC_01127 | 1.9e-78 | ytxH | S | YtxH-like protein | ||
JHHLHNBC_01129 | 1.4e-62 | |||||
JHHLHNBC_01130 | 1.4e-87 | bioY | S | BioY family | ||
JHHLHNBC_01131 | 8.8e-273 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
JHHLHNBC_01132 | 0.0 | cadA | P | P-type ATPase | ||
JHHLHNBC_01133 | 0.0 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
JHHLHNBC_01134 | 1.3e-38 | |||||
JHHLHNBC_01135 | 1.1e-298 | V | ABC transporter transmembrane region | |||
JHHLHNBC_01136 | 7e-292 | V | ABC transporter transmembrane region | |||
JHHLHNBC_01137 | 6.5e-69 | S | Iron-sulphur cluster biosynthesis | |||
JHHLHNBC_01138 | 0.0 | XK27_08510 | L | Type III restriction protein res subunit | ||
JHHLHNBC_01139 | 2.4e-161 | 2.7.1.39 | S | Phosphotransferase enzyme family | ||
JHHLHNBC_01140 | 2.7e-116 | zmp3 | O | Zinc-dependent metalloprotease | ||
JHHLHNBC_01141 | 0.0 | lytN | 3.5.1.104 | M | LysM domain | |
JHHLHNBC_01142 | 4.4e-83 | agaB | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_01143 | 3.7e-124 | agaC | G | PTS system sorbose-specific iic component | ||
JHHLHNBC_01144 | 6.8e-134 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_01145 | 5.5e-66 | G | PTS system fructose IIA component | |||
JHHLHNBC_01146 | 4.5e-61 | |||||
JHHLHNBC_01147 | 8.4e-97 | S | membrane transporter protein | |||
JHHLHNBC_01148 | 1.2e-156 | V | Beta-lactamase | |||
JHHLHNBC_01149 | 4e-111 | S | Domain of unknown function (DUF4867) | |||
JHHLHNBC_01150 | 1.1e-162 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | pfkB family carbohydrate kinase | |
JHHLHNBC_01151 | 1.1e-56 | S | Domain of unknown function (DUF1827) | |||
JHHLHNBC_01152 | 0.0 | ydaO | E | amino acid | ||
JHHLHNBC_01153 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
JHHLHNBC_01154 | 0.0 | typA | T | GTP-binding protein TypA | ||
JHHLHNBC_01155 | 4.2e-209 | ftsW | D | Belongs to the SEDS family | ||
JHHLHNBC_01156 | 1.3e-139 | dkgB | S | reductase | ||
JHHLHNBC_01157 | 2.9e-84 | nrdI | F | Belongs to the NrdI family | ||
JHHLHNBC_01158 | 8e-179 | D | Alpha beta | |||
JHHLHNBC_01159 | 1.5e-77 | K | Transcriptional regulator | |||
JHHLHNBC_01160 | 1e-119 | gph | 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
JHHLHNBC_01161 | 4.2e-193 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
JHHLHNBC_01162 | 3.4e-94 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
JHHLHNBC_01163 | 1.8e-59 | |||||
JHHLHNBC_01164 | 4.8e-176 | 3.4.11.5 | I | Releases the N-terminal proline from various substrates | ||
JHHLHNBC_01165 | 0.0 | yfgQ | P | E1-E2 ATPase | ||
JHHLHNBC_01166 | 1.1e-59 | |||||
JHHLHNBC_01167 | 2.5e-77 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
JHHLHNBC_01168 | 4.6e-236 | 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 | |
JHHLHNBC_01169 | 2.2e-224 | 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 | |
JHHLHNBC_01170 | 3.1e-69 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
JHHLHNBC_01171 | 1.1e-31 | ywzB | S | Protein of unknown function (DUF1146) | ||
JHHLHNBC_01172 | 1.1e-101 | Q | methyltransferase activity | |||
JHHLHNBC_01173 | 2.1e-90 | T | Sh3 type 3 domain protein | |||
JHHLHNBC_01174 | 1.9e-115 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
JHHLHNBC_01175 | 6.7e-136 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
JHHLHNBC_01176 | 4.2e-119 | tcyB | E | ABC transporter | ||
JHHLHNBC_01177 | 4.3e-144 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
JHHLHNBC_01178 | 1.8e-209 | metC | 4.4.1.8 | E | cystathionine | |
JHHLHNBC_01179 | 3.3e-141 | |||||
JHHLHNBC_01181 | 7.8e-174 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
JHHLHNBC_01182 | 1.5e-152 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
JHHLHNBC_01183 | 1.5e-77 | fic | D | Fic/DOC family | ||
JHHLHNBC_01184 | 5.7e-62 | |||||
JHHLHNBC_01185 | 1.6e-31 | |||||
JHHLHNBC_01186 | 6.7e-63 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_01187 | 1.1e-37 | |||||
JHHLHNBC_01188 | 4.4e-101 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
JHHLHNBC_01189 | 1.6e-64 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
JHHLHNBC_01190 | 4.4e-172 | prmA | J | Ribosomal protein L11 methyltransferase | ||
JHHLHNBC_01191 | 2.1e-126 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
JHHLHNBC_01192 | 1e-48 | |||||
JHHLHNBC_01193 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
JHHLHNBC_01194 | 1.2e-74 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
JHHLHNBC_01195 | 3.1e-118 | 3.1.3.18 | J | HAD-hyrolase-like | ||
JHHLHNBC_01196 | 5.7e-247 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
JHHLHNBC_01197 | 4e-92 | S | Protein of unknown function (DUF1440) | |||
JHHLHNBC_01198 | 5.8e-247 | G | MFS/sugar transport protein | |||
JHHLHNBC_01199 | 2.4e-275 | ycaM | E | amino acid | ||
JHHLHNBC_01200 | 4.7e-73 | |||||
JHHLHNBC_01201 | 2e-123 | |||||
JHHLHNBC_01202 | 2.3e-124 | S | Tetratricopeptide repeat | |||
JHHLHNBC_01203 | 2.3e-147 | |||||
JHHLHNBC_01204 | 1.1e-261 | 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 | |
JHHLHNBC_01205 | 1.5e-160 | yjjH | S | Calcineurin-like phosphoesterase | ||
JHHLHNBC_01206 | 1.5e-264 | dtpT | U | amino acid peptide transporter | ||
JHHLHNBC_01207 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01208 | 2.4e-57 | |||||
JHHLHNBC_01209 | 1.6e-73 | S | function, without similarity to other proteins | |||
JHHLHNBC_01210 | 7.6e-245 | G | MFS/sugar transport protein | |||
JHHLHNBC_01211 | 2.9e-56 | |||||
JHHLHNBC_01212 | 0.0 | pckG | 4.1.1.32, 4.1.1.49 | C | Phosphoenolpyruvate carboxykinase | |
JHHLHNBC_01213 | 5.1e-23 | S | Virus attachment protein p12 family | |||
JHHLHNBC_01214 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
JHHLHNBC_01215 | 1.1e-83 | feoA | P | FeoA | ||
JHHLHNBC_01216 | 2.4e-120 | E | lipolytic protein G-D-S-L family | |||
JHHLHNBC_01217 | 6.8e-107 | kch | J | Ion transport protein | ||
JHHLHNBC_01219 | 1e-169 | L | Transposase DDE domain | |||
JHHLHNBC_01223 | 2e-80 | S | Siphovirus Gp157 | |||
JHHLHNBC_01224 | 4.9e-128 | S | AAA domain | |||
JHHLHNBC_01225 | 2.9e-99 | S | Protein of unknown function (DUF669) | |||
JHHLHNBC_01226 | 3.3e-80 | S | calcium ion binding | |||
JHHLHNBC_01227 | 1.8e-123 | dnaC | 3.4.21.53 | L | IstB-like ATP binding protein | |
JHHLHNBC_01229 | 7.5e-118 | yjjP | S | Putative threonine/serine exporter | ||
JHHLHNBC_01230 | 2.1e-126 | S | Protein of unknown function (DUF975) | |||
JHHLHNBC_01231 | 7.7e-55 | yqkB | S | Iron-sulphur cluster biosynthesis | ||
JHHLHNBC_01232 | 9e-53 | |||||
JHHLHNBC_01234 | 2.7e-82 | S | Bacterial PH domain | |||
JHHLHNBC_01235 | 3.2e-286 | ydbT | S | Bacterial PH domain | ||
JHHLHNBC_01236 | 5.7e-138 | S | AAA ATPase domain | |||
JHHLHNBC_01237 | 2.5e-169 | yniA | G | Phosphotransferase enzyme family | ||
JHHLHNBC_01238 | 2e-66 | V | ABC-2 type transporter | |||
JHHLHNBC_01239 | 1.6e-51 | V | ABC-type multidrug transport system ATPase component | |||
JHHLHNBC_01240 | 3.6e-30 | K | sequence-specific DNA binding | |||
JHHLHNBC_01241 | 9.6e-21 | K | sequence-specific DNA binding | |||
JHHLHNBC_01242 | 1.5e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_01243 | 2.5e-256 | glnP | P | ABC transporter | ||
JHHLHNBC_01244 | 1.9e-23 | glnP | P | ABC transporter | ||
JHHLHNBC_01245 | 1.1e-246 | glnP | P | ABC transporter | ||
JHHLHNBC_01246 | 1.2e-100 | ydaF | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_01247 | 1.9e-127 | K | UbiC transcription regulator-associated domain protein | |||
JHHLHNBC_01248 | 3.7e-238 | 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 | |||
JHHLHNBC_01249 | 0.0 | mngB | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
JHHLHNBC_01250 | 8.9e-245 | S | Metal-independent alpha-mannosidase (GH125) | |||
JHHLHNBC_01251 | 3.9e-154 | ypbG | 2.7.1.2 | GK | ROK family | |
JHHLHNBC_01252 | 1.8e-286 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JHHLHNBC_01253 | 6.5e-48 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_01254 | 8.6e-270 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
JHHLHNBC_01255 | 1.3e-270 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
JHHLHNBC_01256 | 5.3e-170 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
JHHLHNBC_01257 | 2.7e-55 | ysxB | J | Cysteine protease Prp | ||
JHHLHNBC_01258 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
JHHLHNBC_01259 | 3.8e-32 | |||||
JHHLHNBC_01260 | 4.1e-14 | |||||
JHHLHNBC_01261 | 2.5e-233 | ywhK | S | Membrane | ||
JHHLHNBC_01263 | 4.2e-300 | V | ABC transporter transmembrane region | |||
JHHLHNBC_01264 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
JHHLHNBC_01267 | 4.1e-81 | S | Siphovirus Gp157 | |||
JHHLHNBC_01268 | 1.3e-41 | S | ERF superfamily | |||
JHHLHNBC_01269 | 1.1e-121 | S | Pfam:HNHc_6 | |||
JHHLHNBC_01270 | 1.2e-54 | S | HNH endonuclease | |||
JHHLHNBC_01271 | 2.3e-59 | S | Single-strand binding protein family | |||
JHHLHNBC_01272 | 6.9e-113 | S | calcium ion binding | |||
JHHLHNBC_01273 | 1.1e-234 | S | DNA helicase activity | |||
JHHLHNBC_01276 | 4.4e-103 | 3.2.2.20 | K | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_01277 | 9e-92 | yxjI | ||||
JHHLHNBC_01278 | 2e-158 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_01279 | 5.1e-237 | S | Tetratricopeptide repeat protein | |||
JHHLHNBC_01280 | 4.8e-149 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
JHHLHNBC_01281 | 3.6e-224 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
JHHLHNBC_01282 | 9.6e-85 | |||||
JHHLHNBC_01283 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01284 | 9.4e-27 | |||||
JHHLHNBC_01286 | 2.1e-152 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
JHHLHNBC_01288 | 7e-182 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
JHHLHNBC_01289 | 4.5e-121 | azlC | E | branched-chain amino acid | ||
JHHLHNBC_01290 | 1.5e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
JHHLHNBC_01291 | 1.5e-42 | yrzL | S | Belongs to the UPF0297 family | ||
JHHLHNBC_01292 | 9.5e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
JHHLHNBC_01293 | 2.8e-84 | perR | P | Belongs to the Fur family | ||
JHHLHNBC_01294 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
JHHLHNBC_01295 | 7e-90 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
JHHLHNBC_01296 | 3.3e-60 | spl | M | NlpC/P60 family | ||
JHHLHNBC_01297 | 5.3e-245 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
JHHLHNBC_01298 | 8.1e-175 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
JHHLHNBC_01299 | 8.8e-142 | mreB | D | cell shape determining protein MreB | ||
JHHLHNBC_01300 | 4.6e-171 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_01301 | 1.1e-150 | mreC | M | Involved in formation and maintenance of cell shape | ||
JHHLHNBC_01302 | 1.5e-89 | mreD | M | rod shape-determining protein MreD | ||
JHHLHNBC_01303 | 1.2e-112 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
JHHLHNBC_01304 | 1.5e-141 | minD | D | Belongs to the ParA family | ||
JHHLHNBC_01305 | 1.6e-109 | artQ | P | ABC transporter permease | ||
JHHLHNBC_01306 | 5.8e-112 | glnQ | 3.6.3.21 | E | ABC transporter | |
JHHLHNBC_01307 | 4e-150 | aatB | ET | ABC transporter substrate-binding protein | ||
JHHLHNBC_01308 | 5.6e-272 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
JHHLHNBC_01309 | 4.9e-54 | |||||
JHHLHNBC_01310 | 2.4e-77 | mraZ | K | Belongs to the MraZ family | ||
JHHLHNBC_01311 | 4.1e-170 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
JHHLHNBC_01312 | 6.4e-55 | ftsL | D | cell division protein FtsL | ||
JHHLHNBC_01313 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
JHHLHNBC_01314 | 9.2e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
JHHLHNBC_01315 | 8.3e-265 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
JHHLHNBC_01316 | 5.1e-201 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
JHHLHNBC_01317 | 8.3e-154 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
JHHLHNBC_01318 | 0.0 | oatA | I | Acyltransferase | ||
JHHLHNBC_01319 | 4.4e-244 | 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 | ||
JHHLHNBC_01320 | 0.0 | oatA | I | Acyltransferase | ||
JHHLHNBC_01321 | 1.1e-18 | 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 | ||
JHHLHNBC_01322 | 2.5e-135 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
JHHLHNBC_01324 | 2.3e-242 | pts36C | G | PTS system sugar-specific permease component | ||
JHHLHNBC_01325 | 5.2e-53 | sgcB | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_01326 | 8.6e-84 | pts36A | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_01327 | 3.3e-133 | K | DeoR C terminal sensor domain | |||
JHHLHNBC_01328 | 2.6e-174 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
JHHLHNBC_01329 | 2.2e-256 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
JHHLHNBC_01330 | 2e-57 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
JHHLHNBC_01331 | 8.4e-263 | rhaB | 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
JHHLHNBC_01332 | 3.3e-213 | iolF | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01333 | 1e-182 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
JHHLHNBC_01334 | 3.8e-215 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
JHHLHNBC_01335 | 2.9e-284 | ygcU | 2.5.1.26 | C | FAD linked oxidases, C-terminal domain | |
JHHLHNBC_01336 | 1.2e-285 | ygcE | 2.7.1.17 | G | Belongs to the FGGY kinase family | |
JHHLHNBC_01337 | 1.3e-94 | ygcP | K | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | ||
JHHLHNBC_01338 | 9e-209 | gldA | 1.1.1.6 | C | dehydrogenase | |
JHHLHNBC_01342 | 5.8e-29 | L | RelB antitoxin | |||
JHHLHNBC_01344 | 1.5e-08 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_01345 | 2.3e-150 | ydbD | P | Manganese containing catalase | ||
JHHLHNBC_01346 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
JHHLHNBC_01349 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_01351 | 3.5e-107 | 3.6.1.27 | I | Acid phosphatase homologues | ||
JHHLHNBC_01352 | 3.1e-117 | S | Domain of unknown function (DUF4811) | |||
JHHLHNBC_01353 | 2.3e-265 | lmrB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01354 | 1e-87 | merR | K | MerR HTH family regulatory protein | ||
JHHLHNBC_01355 | 4.3e-267 | emrY | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01356 | 4.6e-90 | |||||
JHHLHNBC_01357 | 6.6e-117 | ydfK | S | Protein of unknown function (DUF554) | ||
JHHLHNBC_01358 | 1.4e-180 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
JHHLHNBC_01359 | 1.5e-225 | EK | Aminotransferase, class I | |||
JHHLHNBC_01360 | 5.8e-166 | K | LysR substrate binding domain | |||
JHHLHNBC_01361 | 6.2e-90 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
JHHLHNBC_01362 | 5.4e-147 | yitU | 3.1.3.104 | S | hydrolase | |
JHHLHNBC_01364 | 1.5e-19 | |||||
JHHLHNBC_01365 | 6.1e-258 | bmr3 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01366 | 4.9e-45 | S | Thiamine-binding protein | |||
JHHLHNBC_01367 | 2.9e-136 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
JHHLHNBC_01368 | 2.8e-159 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase superfamily domain | |
JHHLHNBC_01369 | 2.5e-242 | sgaT | 2.7.1.194 | S | PTS system sugar-specific permease component | |
JHHLHNBC_01370 | 4.9e-162 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_01371 | 4.2e-286 | 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
JHHLHNBC_01372 | 9.8e-135 | K | DeoR C terminal sensor domain | |||
JHHLHNBC_01373 | 1.7e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
JHHLHNBC_01374 | 8.4e-254 | rarA | L | recombination factor protein RarA | ||
JHHLHNBC_01375 | 1.2e-57 | |||||
JHHLHNBC_01376 | 9.1e-173 | yhaI | S | Protein of unknown function (DUF805) | ||
JHHLHNBC_01377 | 7.6e-269 | K | Mga helix-turn-helix domain | |||
JHHLHNBC_01378 | 4.8e-167 | ynjC | S | Cell surface protein | ||
JHHLHNBC_01379 | 6.7e-123 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_01381 | 1.9e-310 | |||||
JHHLHNBC_01382 | 2.4e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
JHHLHNBC_01383 | 0.0 | ylbB | V | ABC transporter permease | ||
JHHLHNBC_01384 | 6.9e-125 | usp | 3.5.1.28 | CBM50 | D | CHAP domain |
JHHLHNBC_01385 | 7e-203 | P | Pyridine nucleotide-disulphide oxidoreductase | |||
JHHLHNBC_01386 | 1.1e-190 | amtB | P | Ammonium Transporter Family | ||
JHHLHNBC_01387 | 1.2e-68 | psiE | S | Phosphate-starvation-inducible E | ||
JHHLHNBC_01388 | 1.7e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
JHHLHNBC_01389 | 1.9e-197 | yfjR | K | WYL domain | ||
JHHLHNBC_01391 | 1.3e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
JHHLHNBC_01392 | 2.2e-183 | |||||
JHHLHNBC_01393 | 2.4e-157 | S | Putative esterase | |||
JHHLHNBC_01394 | 7e-11 | S | response to antibiotic | |||
JHHLHNBC_01395 | 3.7e-67 | K | MarR family | |||
JHHLHNBC_01396 | 9.8e-83 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
JHHLHNBC_01397 | 6e-61 | P | Rhodanese-like domain | |||
JHHLHNBC_01398 | 1.1e-25 | |||||
JHHLHNBC_01399 | 2.9e-199 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
JHHLHNBC_01400 | 6.7e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
JHHLHNBC_01401 | 1.9e-124 | ftsE | D | ABC transporter | ||
JHHLHNBC_01402 | 6.6e-187 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
JHHLHNBC_01403 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
JHHLHNBC_01404 | 3.3e-86 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
JHHLHNBC_01405 | 2.4e-173 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
JHHLHNBC_01406 | 4.2e-102 | Q | methyltransferase | |||
JHHLHNBC_01407 | 9.4e-101 | T | Sh3 type 3 domain protein | |||
JHHLHNBC_01408 | 2.1e-114 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
JHHLHNBC_01409 | 8.8e-136 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
JHHLHNBC_01410 | 2e-101 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
JHHLHNBC_01411 | 5.3e-161 | 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 | |
JHHLHNBC_01412 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
JHHLHNBC_01413 | 1e-112 | ybhL | S | Inhibitor of apoptosis-promoting Bax1 | ||
JHHLHNBC_01414 | 8.4e-174 | S | Cell surface protein | |||
JHHLHNBC_01416 | 1.2e-132 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_01417 | 0.0 | N | domain, Protein | |||
JHHLHNBC_01418 | 5.5e-278 | K | transcriptional antiterminator | |||
JHHLHNBC_01419 | 6.8e-256 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
JHHLHNBC_01420 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
JHHLHNBC_01421 | 5.8e-112 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
JHHLHNBC_01422 | 6.5e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
JHHLHNBC_01424 | 1.9e-118 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
JHHLHNBC_01425 | 8.8e-147 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
JHHLHNBC_01426 | 4.5e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
JHHLHNBC_01427 | 1.4e-25 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
JHHLHNBC_01428 | 2.4e-55 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
JHHLHNBC_01429 | 1.3e-31 | S | Protein of unknown function (DUF2969) | |||
JHHLHNBC_01430 | 5.8e-222 | rodA | D | Belongs to the SEDS family | ||
JHHLHNBC_01431 | 3.6e-48 | gcvH | E | glycine cleavage | ||
JHHLHNBC_01432 | 4.9e-159 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
JHHLHNBC_01433 | 1.7e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
JHHLHNBC_01434 | 7e-203 | ypdF | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
JHHLHNBC_01435 | 6.3e-102 | 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 | ||
JHHLHNBC_01436 | 2e-77 | yqhY | S | Asp23 family, cell envelope-related function | ||
JHHLHNBC_01437 | 2e-66 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
JHHLHNBC_01438 | 5e-151 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
JHHLHNBC_01439 | 1e-246 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
JHHLHNBC_01440 | 1.6e-32 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
JHHLHNBC_01441 | 9.4e-150 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JHHLHNBC_01442 | 3e-153 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
JHHLHNBC_01443 | 2e-74 | argR | K | Regulates arginine biosynthesis genes | ||
JHHLHNBC_01444 | 6.1e-310 | recN | L | May be involved in recombinational repair of damaged DNA | ||
JHHLHNBC_01445 | 6e-51 | |||||
JHHLHNBC_01446 | 2.1e-123 | rssA | S | Patatin-like phospholipase | ||
JHHLHNBC_01447 | 3.2e-115 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
JHHLHNBC_01448 | 2.9e-35 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
JHHLHNBC_01449 | 7.3e-217 | 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 | |
JHHLHNBC_01450 | 2.6e-91 | manY | G | PTS system | ||
JHHLHNBC_01451 | 8.4e-279 | 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) | |
JHHLHNBC_01452 | 7.3e-256 | iolT | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01453 | 3.2e-104 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
JHHLHNBC_01454 | 1.9e-78 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
JHHLHNBC_01455 | 5.8e-208 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
JHHLHNBC_01456 | 1.2e-134 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
JHHLHNBC_01457 | 2.2e-41 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JHHLHNBC_01458 | 9.6e-129 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JHHLHNBC_01459 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JHHLHNBC_01460 | 5.3e-278 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
JHHLHNBC_01461 | 2.5e-186 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
JHHLHNBC_01462 | 1e-99 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
JHHLHNBC_01463 | 1.6e-288 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
JHHLHNBC_01464 | 2.8e-235 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
JHHLHNBC_01465 | 1.4e-75 | copR | K | Copper transport repressor CopY TcrY | ||
JHHLHNBC_01466 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
JHHLHNBC_01467 | 6.4e-110 | 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 | |
JHHLHNBC_01468 | 1.5e-205 | T | PhoQ Sensor | |||
JHHLHNBC_01469 | 3.6e-120 | K | response regulator | |||
JHHLHNBC_01470 | 9.7e-138 | bceA | V | ABC transporter | ||
JHHLHNBC_01471 | 0.0 | V | ABC transporter (permease) | |||
JHHLHNBC_01472 | 2.4e-92 | traP | 1.14.99.57, 6.2.1.3 | S | heme oxygenase (decyclizing) activity | |
JHHLHNBC_01473 | 2.1e-137 | yhfI | S | Metallo-beta-lactamase superfamily | ||
JHHLHNBC_01474 | 1.5e-65 | 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 | |
JHHLHNBC_01475 | 1.9e-121 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
JHHLHNBC_01476 | 3.3e-301 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
JHHLHNBC_01477 | 3.8e-176 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
JHHLHNBC_01478 | 1e-08 | |||||
JHHLHNBC_01479 | 7.7e-67 | |||||
JHHLHNBC_01480 | 1.3e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
JHHLHNBC_01481 | 1.3e-210 | 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 | |
JHHLHNBC_01482 | 2.1e-160 | mleR | K | LysR family | ||
JHHLHNBC_01483 | 8.6e-173 | corA | P | CorA-like Mg2+ transporter protein | ||
JHHLHNBC_01484 | 3.3e-61 | yeaO | S | Protein of unknown function, DUF488 | ||
JHHLHNBC_01485 | 5.2e-104 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
JHHLHNBC_01486 | 3.9e-96 | |||||
JHHLHNBC_01487 | 7.9e-106 | ywrF | S | Flavin reductase like domain | ||
JHHLHNBC_01488 | 2.9e-168 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
JHHLHNBC_01489 | 8.8e-73 | |||||
JHHLHNBC_01490 | 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 | ||
JHHLHNBC_01491 | 8.6e-93 | cvpA | S | Colicin V production protein | ||
JHHLHNBC_01492 | 2e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
JHHLHNBC_01493 | 2.3e-53 | yrzB | S | Belongs to the UPF0473 family | ||
JHHLHNBC_01494 | 9.5e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
JHHLHNBC_01495 | 4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
JHHLHNBC_01496 | 1e-77 | metI | P | ABC transporter permease | ||
JHHLHNBC_01497 | 1.9e-141 | sufC | O | FeS assembly ATPase SufC | ||
JHHLHNBC_01498 | 4.1e-192 | sufD | O | FeS assembly protein SufD | ||
JHHLHNBC_01499 | 1.2e-227 | csdA | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
JHHLHNBC_01500 | 2.9e-78 | nifU | C | SUF system FeS assembly protein, NifU family | ||
JHHLHNBC_01501 | 5.6e-280 | sufB | O | assembly protein SufB | ||
JHHLHNBC_01502 | 1.8e-26 | |||||
JHHLHNBC_01503 | 4.9e-66 | yueI | S | Protein of unknown function (DUF1694) | ||
JHHLHNBC_01504 | 5.8e-180 | S | Protein of unknown function (DUF2785) | |||
JHHLHNBC_01505 | 9.7e-158 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
JHHLHNBC_01506 | 1.5e-83 | usp6 | T | universal stress protein | ||
JHHLHNBC_01507 | 1.7e-39 | |||||
JHHLHNBC_01508 | 1.5e-153 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JHHLHNBC_01509 | 2.8e-137 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
JHHLHNBC_01510 | 0.0 | clpL | O | associated with various cellular activities | ||
JHHLHNBC_01511 | 4.4e-65 | nrp | 1.20.4.1 | P | ArsC family | |
JHHLHNBC_01512 | 0.0 | fbp | 3.1.3.11 | G | phosphatase activity | |
JHHLHNBC_01513 | 2.8e-143 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
JHHLHNBC_01514 | 2.9e-136 | ylcC | 3.4.22.70 | M | Sortase family | |
JHHLHNBC_01515 | 2.3e-203 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
JHHLHNBC_01516 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
JHHLHNBC_01517 | 2.9e-53 | yneR | S | Belongs to the HesB IscA family | ||
JHHLHNBC_01518 | 2e-115 | vraR | K | helix_turn_helix, Lux Regulon | ||
JHHLHNBC_01519 | 6.4e-137 | yknV | V | ABC transporter | ||
JHHLHNBC_01522 | 8.3e-221 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
JHHLHNBC_01524 | 2.9e-179 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JHHLHNBC_01525 | 5.2e-99 | gerCA | 2.5.1.30 | S | Heptaprenyl diphosphate synthase component I | |
JHHLHNBC_01526 | 1.7e-81 | ynhH | S | NusG domain II | ||
JHHLHNBC_01527 | 1.4e-223 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
JHHLHNBC_01528 | 5.9e-53 | |||||
JHHLHNBC_01529 | 1.3e-85 | |||||
JHHLHNBC_01530 | 8.9e-105 | S | Membrane | |||
JHHLHNBC_01531 | 8.1e-287 | pipD | E | Dipeptidase | ||
JHHLHNBC_01532 | 3.8e-54 | |||||
JHHLHNBC_01533 | 5e-113 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
JHHLHNBC_01534 | 8e-103 | S | Protein of unknown function (DUF1211) | |||
JHHLHNBC_01535 | 1.2e-127 | S | membrane transporter protein | |||
JHHLHNBC_01536 | 2.9e-153 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_01537 | 3e-96 | K | transcriptional regulator | |||
JHHLHNBC_01538 | 1.4e-128 | S | membrane transporter protein | |||
JHHLHNBC_01539 | 3.7e-39 | |||||
JHHLHNBC_01540 | 2.3e-153 | supH | G | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_01541 | 1.8e-98 | K | transcriptional regulator | |||
JHHLHNBC_01542 | 1.4e-122 | macB | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01543 | 0.0 | ylbB | V | ABC transporter permease | ||
JHHLHNBC_01544 | 1.7e-123 | usp | 3.5.1.28 | CBM50 | D | CHAP domain |
JHHLHNBC_01546 | 3.5e-199 | S | peptidoglycan catabolic process | |||
JHHLHNBC_01549 | 3.3e-54 | |||||
JHHLHNBC_01551 | 6.5e-31 | |||||
JHHLHNBC_01552 | 0.0 | S | peptidoglycan catabolic process | |||
JHHLHNBC_01553 | 1.7e-139 | S | Phage tail protein | |||
JHHLHNBC_01554 | 1.4e-167 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
JHHLHNBC_01555 | 1.1e-184 | celB | 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 | |
JHHLHNBC_01556 | 1.1e-210 | mutY | L | A G-specific adenine glycosylase | ||
JHHLHNBC_01557 | 1.9e-149 | cytC6 | I | alpha/beta hydrolase fold | ||
JHHLHNBC_01558 | 5.9e-121 | yrkL | S | Flavodoxin-like fold | ||
JHHLHNBC_01560 | 8.2e-88 | S | Short repeat of unknown function (DUF308) | |||
JHHLHNBC_01561 | 3e-153 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
JHHLHNBC_01562 | 2.7e-199 | |||||
JHHLHNBC_01563 | 3.9e-07 | |||||
JHHLHNBC_01564 | 4e-116 | ywnB | S | NmrA-like family | ||
JHHLHNBC_01565 | 4.6e-118 | ybhL | S | Inhibitor of apoptosis-promoting Bax1 | ||
JHHLHNBC_01566 | 5e-80 | S | Short repeat of unknown function (DUF308) | |||
JHHLHNBC_01567 | 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 | ||
JHHLHNBC_01568 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
JHHLHNBC_01569 | 4.7e-117 | yfbR | S | HD containing hydrolase-like enzyme | ||
JHHLHNBC_01570 | 2.1e-247 | V | FtsX-like permease family | |||
JHHLHNBC_01571 | 1.5e-91 | V | ABC transporter | |||
JHHLHNBC_01572 | 1.2e-114 | T | His Kinase A (phosphoacceptor) domain | |||
JHHLHNBC_01573 | 1.5e-83 | T | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_01574 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
JHHLHNBC_01575 | 1.5e-180 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
JHHLHNBC_01576 | 1.8e-195 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
JHHLHNBC_01577 | 1.1e-155 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
JHHLHNBC_01578 | 1.8e-173 | 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 | ||
JHHLHNBC_01579 | 1.3e-46 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
JHHLHNBC_01580 | 2.1e-31 | |||||
JHHLHNBC_01581 | 7.5e-211 | yvlB | S | Putative adhesin | ||
JHHLHNBC_01582 | 1e-234 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
JHHLHNBC_01583 | 9.3e-259 | arpJ | P | ABC transporter permease | ||
JHHLHNBC_01584 | 1.8e-124 | S | Alpha/beta hydrolase family | |||
JHHLHNBC_01586 | 3.9e-212 | L | Belongs to the 'phage' integrase family | |||
JHHLHNBC_01587 | 3.4e-32 | |||||
JHHLHNBC_01588 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
JHHLHNBC_01590 | 1.4e-173 | yicL | EG | EamA-like transporter family | ||
JHHLHNBC_01591 | 4.8e-286 | |||||
JHHLHNBC_01592 | 7.2e-144 | CcmA5 | V | ABC transporter | ||
JHHLHNBC_01593 | 2.7e-89 | S | ECF-type riboflavin transporter, S component | |||
JHHLHNBC_01594 | 4.2e-147 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
JHHLHNBC_01595 | 1.2e-165 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
JHHLHNBC_01596 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
JHHLHNBC_01597 | 0.0 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01598 | 0.0 | V | ABC transporter | |||
JHHLHNBC_01599 | 7.3e-220 | oxlT | P | Major Facilitator Superfamily | ||
JHHLHNBC_01600 | 3.8e-128 | treR | K | UTRA | ||
JHHLHNBC_01601 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
JHHLHNBC_01602 | 0.0 | treB | G | phosphotransferase system | ||
JHHLHNBC_01603 | 3e-208 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
JHHLHNBC_01604 | 9.5e-259 | yfnA | E | Amino Acid | ||
JHHLHNBC_01605 | 2.1e-171 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
JHHLHNBC_01606 | 1.3e-249 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
JHHLHNBC_01607 | 4e-47 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_01608 | 1.7e-93 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
JHHLHNBC_01609 | 6.1e-73 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
JHHLHNBC_01610 | 5.9e-86 | rfbP | 2.7.8.6 | M | Bacterial sugar transferase | |
JHHLHNBC_01611 | 1.1e-128 | cps1D | M | Domain of unknown function (DUF4422) | ||
JHHLHNBC_01612 | 3e-76 | waaB | GT4 | M | Glycosyl transferases group 1 | |
JHHLHNBC_01613 | 1e-74 | M | Glycosyl transferases group 1 | |||
JHHLHNBC_01614 | 8.1e-42 | M | transferase activity, transferring glycosyl groups | |||
JHHLHNBC_01615 | 5.3e-38 | |||||
JHHLHNBC_01616 | 1.3e-233 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
JHHLHNBC_01617 | 3e-212 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
JHHLHNBC_01618 | 1e-120 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
JHHLHNBC_01619 | 3e-146 | epsB | M | biosynthesis protein | ||
JHHLHNBC_01620 | 1.6e-132 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
JHHLHNBC_01621 | 1.5e-124 | E | lipolytic protein G-D-S-L family | |||
JHHLHNBC_01622 | 5.1e-79 | ccl | S | QueT transporter | ||
JHHLHNBC_01623 | 1.6e-148 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
JHHLHNBC_01624 | 7.6e-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 | ||
JHHLHNBC_01625 | 8.4e-38 | ylqC | S | Belongs to the UPF0109 family | ||
JHHLHNBC_01626 | 3.1e-102 | lemA | S | LemA family | ||
JHHLHNBC_01627 | 6.3e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_01628 | 9.2e-23 | G | Major facilitator Superfamily | |||
JHHLHNBC_01629 | 6.7e-32 | EGP | Major Facilitator Superfamily | |||
JHHLHNBC_01630 | 5.6e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
JHHLHNBC_01631 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
JHHLHNBC_01632 | 2.3e-173 | ccpB | 5.1.1.1 | K | lacI family | |
JHHLHNBC_01633 | 1.7e-59 | |||||
JHHLHNBC_01634 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
JHHLHNBC_01635 | 7.8e-103 | rsmC | 2.1.1.172 | J | Methyltransferase | |
JHHLHNBC_01636 | 1.4e-48 | |||||
JHHLHNBC_01637 | 4.8e-88 | S | QueT transporter | |||
JHHLHNBC_01638 | 1.9e-07 | |||||
JHHLHNBC_01639 | 5.6e-62 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
JHHLHNBC_01640 | 2.4e-37 | |||||
JHHLHNBC_01641 | 6.3e-218 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
JHHLHNBC_01642 | 1.7e-63 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
JHHLHNBC_01643 | 4.5e-264 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
JHHLHNBC_01645 | 1.1e-161 | tas | C | Aldo/keto reductase family | ||
JHHLHNBC_01646 | 1.8e-44 | S | Enterocin A Immunity | |||
JHHLHNBC_01647 | 1.5e-121 | |||||
JHHLHNBC_01648 | 7.3e-133 | |||||
JHHLHNBC_01649 | 1.4e-56 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_01650 | 8.6e-103 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_01651 | 3.9e-192 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
JHHLHNBC_01652 | 5.4e-228 | N | Uncharacterized conserved protein (DUF2075) | |||
JHHLHNBC_01653 | 9.6e-103 | |||||
JHHLHNBC_01654 | 0.0 | M | domain protein | |||
JHHLHNBC_01655 | 1.7e-262 | M | domain protein | |||
JHHLHNBC_01656 | 3.5e-288 | M | Cna protein B-type domain | |||
JHHLHNBC_01657 | 2.6e-133 | 3.4.22.70 | M | Sortase family | ||
JHHLHNBC_01658 | 3.3e-92 | |||||
JHHLHNBC_01660 | 1e-148 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
JHHLHNBC_01661 | 6.3e-227 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
JHHLHNBC_01662 | 4.9e-224 | pimH | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01663 | 8.2e-205 | |||||
JHHLHNBC_01664 | 2.8e-120 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_01665 | 1.5e-76 | ohr | O | OsmC-like protein | ||
JHHLHNBC_01666 | 1.3e-177 | |||||
JHHLHNBC_01667 | 2.3e-110 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
JHHLHNBC_01668 | 1.2e-97 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
JHHLHNBC_01669 | 3.2e-154 | nodB3 | G | Polysaccharide deacetylase | ||
JHHLHNBC_01670 | 1.6e-238 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
JHHLHNBC_01671 | 0.0 | fnq20 | 1.13.12.16 | S | FAD-NAD(P)-binding | |
JHHLHNBC_01672 | 1.2e-147 | gadR | K | Transcriptional activator, Rgg GadR MutR family | ||
JHHLHNBC_01673 | 3.4e-278 | V | ABC transporter transmembrane region | |||
JHHLHNBC_01674 | 6.1e-213 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
JHHLHNBC_01675 | 3.1e-78 | S | NUDIX domain | |||
JHHLHNBC_01676 | 1.1e-75 | |||||
JHHLHNBC_01677 | 2.6e-118 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_01678 | 3e-104 | |||||
JHHLHNBC_01679 | 3.6e-99 | |||||
JHHLHNBC_01680 | 2.8e-108 | |||||
JHHLHNBC_01681 | 2e-302 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_01682 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
JHHLHNBC_01683 | 0.0 | fnq20 | 1.13.12.16 | S | FAD-NAD(P)-binding | |
JHHLHNBC_01684 | 9.3e-164 | gadR | K | Transcriptional activator, Rgg GadR MutR family | ||
JHHLHNBC_01685 | 1.4e-284 | V | ABC transporter transmembrane region | |||
JHHLHNBC_01686 | 2e-106 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
JHHLHNBC_01687 | 1.3e-38 | repA | S | Replication initiator protein A | ||
JHHLHNBC_01688 | 1.1e-214 | yqiG | C | Oxidoreductase | ||
JHHLHNBC_01689 | 7.1e-130 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
JHHLHNBC_01690 | 3e-181 | S | Aldo keto reductase | |||
JHHLHNBC_01691 | 1e-54 | S | Enterocin A Immunity | |||
JHHLHNBC_01692 | 6.4e-54 | |||||
JHHLHNBC_01693 | 1.4e-251 | EGP | Major Facilitator Superfamily | |||
JHHLHNBC_01694 | 2.7e-68 | K | Transcriptional regulator | |||
JHHLHNBC_01695 | 1.7e-132 | S | CAAX protease self-immunity | |||
JHHLHNBC_01699 | 9e-22 | |||||
JHHLHNBC_01700 | 1.1e-41 | spiA | S | Enterocin A Immunity | ||
JHHLHNBC_01702 | 8.9e-131 | plnD | K | LytTr DNA-binding domain | ||
JHHLHNBC_01703 | 7.7e-79 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
JHHLHNBC_01705 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
JHHLHNBC_01706 | 2e-226 | mesE | M | Transport protein ComB | ||
JHHLHNBC_01707 | 7e-59 | |||||
JHHLHNBC_01708 | 2.1e-143 | S | hydrolase | |||
JHHLHNBC_01709 | 2e-58 | |||||
JHHLHNBC_01710 | 4.8e-12 | |||||
JHHLHNBC_01711 | 3e-119 | yoaK | S | Protein of unknown function (DUF1275) | ||
JHHLHNBC_01712 | 4.1e-127 | yjhF | G | Phosphoglycerate mutase family | ||
JHHLHNBC_01713 | 8.4e-154 | S | Protein of unknown function (DUF1211) | |||
JHHLHNBC_01714 | 6.6e-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 | ||
JHHLHNBC_01715 | 1.8e-220 | patA | 2.6.1.1 | E | Aminotransferase | |
JHHLHNBC_01716 | 6.9e-168 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
JHHLHNBC_01717 | 2.7e-196 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
JHHLHNBC_01718 | 1.5e-230 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
JHHLHNBC_01719 | 6.2e-304 | S | Phage plasmid primase, P4 | |||
JHHLHNBC_01720 | 1.6e-58 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
JHHLHNBC_01721 | 4.3e-25 | |||||
JHHLHNBC_01722 | 1.1e-37 | ynzC | S | UPF0291 protein | ||
JHHLHNBC_01723 | 1.1e-28 | yneF | S | UPF0154 protein | ||
JHHLHNBC_01724 | 0.0 | mdlA | V | ABC transporter | ||
JHHLHNBC_01725 | 0.0 | mdlB | V | ABC transporter | ||
JHHLHNBC_01726 | 1.2e-127 | yejC | S | Protein of unknown function (DUF1003) | ||
JHHLHNBC_01727 | 1.4e-211 | yfnA | E | Amino Acid | ||
JHHLHNBC_01728 | 3.7e-122 | plsC | 2.3.1.51 | I | Acyltransferase | |
JHHLHNBC_01729 | 1.9e-130 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
JHHLHNBC_01730 | 1.3e-47 | yazA | L | GIY-YIG catalytic domain protein | ||
JHHLHNBC_01731 | 1.1e-25 | |||||
JHHLHNBC_01732 | 1.1e-37 | ynzC | S | UPF0291 protein | ||
JHHLHNBC_01733 | 4.8e-29 | yneF | S | UPF0154 protein | ||
JHHLHNBC_01734 | 0.0 | mdlA | V | ABC transporter | ||
JHHLHNBC_01735 | 0.0 | mdlB | V | ABC transporter | ||
JHHLHNBC_01736 | 2.6e-138 | yejC | S | Protein of unknown function (DUF1003) | ||
JHHLHNBC_01737 | 9.1e-203 | bcaP | E | Amino Acid | ||
JHHLHNBC_01738 | 1.5e-123 | plsC | 2.3.1.51 | I | Acyltransferase | |
JHHLHNBC_01739 | 4.8e-134 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
JHHLHNBC_01740 | 1.3e-47 | yazA | L | GIY-YIG catalytic domain protein | ||
JHHLHNBC_01741 | 6.8e-170 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
JHHLHNBC_01742 | 5.4e-132 | yfeJ | 6.3.5.2 | F | Glutamine amidotransferase class-I | |
JHHLHNBC_01743 | 1.4e-68 | |||||
JHHLHNBC_01744 | 1.9e-150 | 1.1.1.31 | I | NAD binding domain of 6-phosphogluconate dehydrogenase | ||
JHHLHNBC_01746 | 1.7e-99 | |||||
JHHLHNBC_01747 | 9.6e-121 | dpiA | KT | cheY-homologous receiver domain | ||
JHHLHNBC_01748 | 3.2e-273 | dcuS | 2.7.13.3 | T | Single cache domain 3 | |
JHHLHNBC_01749 | 4.4e-223 | maeN | C | 2-hydroxycarboxylate transporter family | ||
JHHLHNBC_01750 | 4.4e-198 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
JHHLHNBC_01753 | 2.1e-57 | yjdF | S | Protein of unknown function (DUF2992) | ||
JHHLHNBC_01754 | 1.3e-113 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
JHHLHNBC_01755 | 4.6e-154 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_01756 | 1.3e-122 | M1-1017 | ||||
JHHLHNBC_01757 | 4.4e-64 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_01758 | 4.9e-15 | K | Helix-turn-helix domain | |||
JHHLHNBC_01759 | 7.9e-11 | S | Phage derived protein Gp49-like (DUF891) | |||
JHHLHNBC_01761 | 1.4e-229 | steT | E | Amino acid permease | ||
JHHLHNBC_01762 | 6.1e-137 | puuD | S | peptidase C26 | ||
JHHLHNBC_01763 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
JHHLHNBC_01764 | 2.8e-93 | |||||
JHHLHNBC_01765 | 6.5e-98 | |||||
JHHLHNBC_01766 | 2.1e-117 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_01767 | 1.4e-147 | S | Protein of unknown function C-terminus (DUF2399) | |||
JHHLHNBC_01768 | 0.0 | D | Putative exonuclease SbcCD, C subunit | |||
JHHLHNBC_01769 | 6.7e-187 | |||||
JHHLHNBC_01770 | 3e-276 | |||||
JHHLHNBC_01771 | 1.1e-156 | yvfR | V | ABC transporter | ||
JHHLHNBC_01772 | 3.7e-129 | yvfS | V | ABC-2 type transporter | ||
JHHLHNBC_01773 | 9e-201 | desK | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_01774 | 1e-102 | desR | K | helix_turn_helix, Lux Regulon | ||
JHHLHNBC_01775 | 3.9e-170 | |||||
JHHLHNBC_01776 | 2.4e-72 | S | Domain of unknown function (DUF4343) | |||
JHHLHNBC_01777 | 0.0 | cas3 | L | Type III restriction enzyme, res subunit | ||
JHHLHNBC_01778 | 7.2e-169 | csd2 | L | CRISPR-associated protein Cas7 | ||
JHHLHNBC_01779 | 0.0 | csd1 | 3.5.1.28 | M | CRISPR-associated protein (Cas_Csd1) | |
JHHLHNBC_01780 | 1.5e-124 | cas5d | S | CRISPR-associated protein (Cas_Cas5) | ||
JHHLHNBC_01782 | 1.9e-25 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
JHHLHNBC_01783 | 1.2e-138 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
JHHLHNBC_01784 | 5.3e-68 | cas4 | 3.1.12.1 | L | Domain of unknown function DUF83 | |
JHHLHNBC_01785 | 6.6e-68 | gst | 2.5.1.18 | O | Glutathione S-transferase, C-terminal domain | |
JHHLHNBC_01786 | 6.2e-21 | gst | 2.5.1.18 | O | Glutathione S-transferase, C-terminal domain | |
JHHLHNBC_01787 | 3.2e-39 | cadC1 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
JHHLHNBC_01788 | 1.1e-56 | |||||
JHHLHNBC_01789 | 3.5e-127 | S | ABC-2 family transporter protein | |||
JHHLHNBC_01790 | 3.1e-146 | bcrA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
JHHLHNBC_01791 | 2.1e-120 | T | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_01792 | 2.3e-154 | T | GHKL domain | |||
JHHLHNBC_01793 | 9.8e-305 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_01794 | 7.8e-154 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
JHHLHNBC_01795 | 2.2e-131 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
JHHLHNBC_01796 | 5.6e-135 | pnuC | H | nicotinamide mononucleotide transporter | ||
JHHLHNBC_01797 | 1.3e-165 | IQ | NAD dependent epimerase/dehydratase family | |||
JHHLHNBC_01798 | 7.8e-149 | 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 | |
JHHLHNBC_01799 | 6.3e-123 | G | Phosphoglycerate mutase family | |||
JHHLHNBC_01800 | 5.2e-148 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
JHHLHNBC_01801 | 8.4e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
JHHLHNBC_01802 | 1.3e-108 | yktB | S | Belongs to the UPF0637 family | ||
JHHLHNBC_01803 | 7.2e-77 | yueI | S | Protein of unknown function (DUF1694) | ||
JHHLHNBC_01804 | 0.0 | 6.3.2.2, 6.3.2.4 | M | Mur ligase middle domain protein | ||
JHHLHNBC_01805 | 4.7e-171 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
JHHLHNBC_01806 | 0.0 | V | FtsX-like permease family | |||
JHHLHNBC_01807 | 4e-136 | cysA | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01808 | 0.0 | E | amino acid | |||
JHHLHNBC_01809 | 3.7e-165 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
JHHLHNBC_01810 | 1e-165 | XK27_00670 | S | ABC transporter substrate binding protein | ||
JHHLHNBC_01811 | 6.5e-160 | S | PTS system sugar-specific permease component | |||
JHHLHNBC_01812 | 1.9e-25 | 2.7.1.194 | G | protein-N(PI)-phosphohistidine-sugar phosphotransferase activity | ||
JHHLHNBC_01813 | 2.2e-132 | S | N-acetylphosphatidylethanolamine-hydrolysing phospholipas activity | |||
JHHLHNBC_01814 | 9.3e-67 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_01815 | 6.6e-219 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
JHHLHNBC_01816 | 3.6e-210 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
JHHLHNBC_01817 | 2.1e-37 | glvR | K | Helix-turn-helix domain, rpiR family | ||
JHHLHNBC_01819 | 2.9e-19 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
JHHLHNBC_01820 | 1.2e-43 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
JHHLHNBC_01821 | 4.2e-52 | 5.4.2.6 | S | Haloacid dehalogenase-like hydrolase | ||
JHHLHNBC_01822 | 2.5e-227 | manR | K | PRD domain | ||
JHHLHNBC_01823 | 1.4e-27 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |
JHHLHNBC_01824 | 2.7e-166 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_01825 | 7.7e-61 | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_01826 | 4.7e-46 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_01827 | 9.4e-163 | G | Phosphotransferase System | |||
JHHLHNBC_01828 | 2.8e-126 | G | Domain of unknown function (DUF4432) | |||
JHHLHNBC_01829 | 2.8e-112 | 5.3.1.15 | S | Pfam:DUF1498 | ||
JHHLHNBC_01830 | 6.7e-196 | xylB | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
JHHLHNBC_01831 | 7.2e-61 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_01832 | 9e-268 | frvB | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_01833 | 4e-191 | malY | 4.4.1.8 | E | Aminotransferase class I and II | |
JHHLHNBC_01834 | 2.2e-219 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
JHHLHNBC_01835 | 9.6e-64 | kdsD | 5.3.1.13 | M | SIS domain | |
JHHLHNBC_01836 | 2.9e-44 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_01837 | 3e-31 | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_01838 | 2.5e-183 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
JHHLHNBC_01839 | 1.6e-86 | 4.3.3.7 | E | Dihydrodipicolinate synthetase family | ||
JHHLHNBC_01840 | 8.4e-71 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
JHHLHNBC_01841 | 9e-197 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_01842 | 1.9e-18 | hxlR | K | Transcriptional regulator, HxlR family | ||
JHHLHNBC_01843 | 3.3e-57 | pnb | C | nitroreductase | ||
JHHLHNBC_01844 | 2.5e-119 | |||||
JHHLHNBC_01845 | 1.5e-07 | K | DNA-templated transcription, initiation | |||
JHHLHNBC_01846 | 1.3e-17 | S | YvrJ protein family | |||
JHHLHNBC_01847 | 4.3e-146 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
JHHLHNBC_01848 | 7.4e-86 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
JHHLHNBC_01849 | 7.2e-184 | hrtB | V | ABC transporter permease | ||
JHHLHNBC_01850 | 9.6e-121 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
JHHLHNBC_01851 | 3.8e-262 | npr | 1.11.1.1 | C | NADH oxidase | |
JHHLHNBC_01852 | 9.1e-150 | S | hydrolase | |||
JHHLHNBC_01853 | 2.2e-44 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
JHHLHNBC_01854 | 6.6e-137 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
JHHLHNBC_01857 | 3.5e-08 | |||||
JHHLHNBC_01858 | 5.3e-78 | L | Resolvase, N-terminal | |||
JHHLHNBC_01859 | 1.1e-297 | 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 | |
JHHLHNBC_01861 | 3e-262 | L | Exonuclease | |||
JHHLHNBC_01862 | 2.9e-44 | relB | L | RelB antitoxin | ||
JHHLHNBC_01863 | 1.2e-48 | K | Helix-turn-helix domain | |||
JHHLHNBC_01864 | 9.6e-206 | yceJ | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01865 | 8.9e-104 | tag | 3.2.2.20 | L | glycosylase | |
JHHLHNBC_01866 | 1.6e-32 | |||||
JHHLHNBC_01867 | 1.1e-46 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
JHHLHNBC_01868 | 6.9e-72 | K | Transcriptional regulator | |||
JHHLHNBC_01869 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
JHHLHNBC_01870 | 2.2e-97 | vanZ | V | VanZ like family | ||
JHHLHNBC_01871 | 4.5e-152 | glcU | U | sugar transport | ||
JHHLHNBC_01872 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
JHHLHNBC_01873 | 8.8e-72 | ssb_2 | L | Single-strand binding protein family | ||
JHHLHNBC_01874 | 7.4e-72 | EGP | Major Facilitator Superfamily | |||
JHHLHNBC_01875 | 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 | |
JHHLHNBC_01876 | 1.7e-142 | |||||
JHHLHNBC_01877 | 1.5e-99 | S | Tetratricopeptide repeat | |||
JHHLHNBC_01878 | 1.6e-123 | |||||
JHHLHNBC_01879 | 1.2e-73 | |||||
JHHLHNBC_01880 | 1.9e-42 | rpmE2 | J | Ribosomal protein L31 | ||
JHHLHNBC_01881 | 1.2e-109 | S | CAAX protease self-immunity | |||
JHHLHNBC_01882 | 1.4e-130 | ydfF | K | Transcriptional | ||
JHHLHNBC_01883 | 8.4e-134 | nodI | V | ABC transporter | ||
JHHLHNBC_01884 | 2.9e-134 | nodJ | V | ABC-2 type transporter | ||
JHHLHNBC_01885 | 6.4e-32 | ywzB | S | Protein of unknown function (DUF1146) | ||
JHHLHNBC_01886 | 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 | ||
JHHLHNBC_01887 | 3.6e-79 | ctsR | K | Belongs to the CtsR family | ||
JHHLHNBC_01888 | 4e-101 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
JHHLHNBC_01889 | 6.5e-176 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
JHHLHNBC_01890 | 7.8e-252 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
JHHLHNBC_01891 | 1.5e-135 | stp | 3.1.3.16 | T | phosphatase | |
JHHLHNBC_01892 | 8.7e-113 | XK27_02070 | S | Nitroreductase family | ||
JHHLHNBC_01893 | 4.3e-40 | hxlR | K | Transcriptional regulator, HxlR family | ||
JHHLHNBC_01894 | 1.3e-51 | |||||
JHHLHNBC_01895 | 3.6e-137 | XK27_06755 | T | integral membrane protein | ||
JHHLHNBC_01896 | 2e-146 | M | Glycosyltransferase like family 2 | |||
JHHLHNBC_01897 | 6.4e-134 | glcR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_01898 | 9.4e-68 | T | Sh3 type 3 domain protein | |||
JHHLHNBC_01899 | 1.4e-232 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
JHHLHNBC_01900 | 1.7e-199 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JHHLHNBC_01901 | 0.0 | pepF | E | oligoendopeptidase F | ||
JHHLHNBC_01902 | 2.2e-162 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
JHHLHNBC_01903 | 1.5e-155 | T | Calcineurin-like phosphoesterase superfamily domain | |||
JHHLHNBC_01904 | 3e-134 | znuB | U | ABC 3 transport family | ||
JHHLHNBC_01905 | 1.4e-130 | fhuC | P | ABC transporter | ||
JHHLHNBC_01906 | 3.4e-58 | |||||
JHHLHNBC_01907 | 5.2e-211 | gntP | EG | Gluconate | ||
JHHLHNBC_01908 | 3.9e-303 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
JHHLHNBC_01909 | 9.4e-172 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
JHHLHNBC_01910 | 6.5e-179 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
JHHLHNBC_01911 | 3.2e-83 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
JHHLHNBC_01912 | 1.5e-166 | natA | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_01913 | 1.7e-219 | ysdA | CP | ABC-2 family transporter protein | ||
JHHLHNBC_01914 | 3.1e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
JHHLHNBC_01915 | 3.2e-149 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
JHHLHNBC_01916 | 9.8e-166 | murB | 1.3.1.98 | M | Cell wall formation | |
JHHLHNBC_01917 | 0.0 | yjcE | P | Sodium proton antiporter | ||
JHHLHNBC_01918 | 2.9e-96 | puuR | K | Cupin domain | ||
JHHLHNBC_01919 | 0.0 | M | domain protein | |||
JHHLHNBC_01920 | 3.7e-82 | 3.4.23.43 | ||||
JHHLHNBC_01921 | 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 | |
JHHLHNBC_01922 | 4e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
JHHLHNBC_01923 | 2.7e-157 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
JHHLHNBC_01924 | 2.6e-79 | F | nucleoside 2-deoxyribosyltransferase | |||
JHHLHNBC_01925 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
JHHLHNBC_01926 | 6.6e-50 | S | Domain of unknown function (DUF4430) | |||
JHHLHNBC_01927 | 3.5e-86 | S | ECF transporter, substrate-specific component | |||
JHHLHNBC_01928 | 1.8e-98 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Cobalamin adenosyltransferase | |
JHHLHNBC_01929 | 9.8e-256 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
JHHLHNBC_01930 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
JHHLHNBC_01931 | 5.8e-173 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
JHHLHNBC_01932 | 7.7e-244 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
JHHLHNBC_01933 | 1.3e-45 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
JHHLHNBC_01934 | 6.9e-136 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
JHHLHNBC_01935 | 1.7e-53 | |||||
JHHLHNBC_01936 | 1.4e-139 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
JHHLHNBC_01937 | 1e-159 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
JHHLHNBC_01938 | 4e-209 | S | Bacterial protein of unknown function (DUF871) | |||
JHHLHNBC_01939 | 6e-65 | S | Domain of unknown function (DUF3284) | |||
JHHLHNBC_01940 | 6.3e-241 | 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 | ||
JHHLHNBC_01941 | 4.8e-131 | K | UbiC transcription regulator-associated domain protein | |||
JHHLHNBC_01942 | 1.1e-50 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_01943 | 2.1e-52 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
JHHLHNBC_01944 | 1.5e-108 | speG | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_01945 | 8.4e-82 | F | NUDIX domain | |||
JHHLHNBC_01946 | 3.9e-84 | S | AAA domain | |||
JHHLHNBC_01947 | 3e-139 | jag | S | R3H domain protein | ||
JHHLHNBC_01948 | 2.5e-253 | 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 | ||
JHHLHNBC_01949 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
JHHLHNBC_01950 | 3.9e-31 | |||||
JHHLHNBC_01952 | 7.1e-133 | thrE | S | Putative threonine/serine exporter | ||
JHHLHNBC_01953 | 1e-79 | S | Threonine/Serine exporter, ThrE | |||
JHHLHNBC_01954 | 3e-201 | gldA | 1.1.1.1, 1.1.1.6 | C | dehydrogenase | |
JHHLHNBC_01955 | 4.6e-149 | P | NLPA lipoprotein | |||
JHHLHNBC_01956 | 5.1e-142 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
JHHLHNBC_01957 | 3.7e-221 | mtnE | 2.6.1.83 | E | Aminotransferase | |
JHHLHNBC_01958 | 5.2e-207 | bacI | V | MacB-like periplasmic core domain | ||
JHHLHNBC_01959 | 5.8e-126 | V | ABC transporter | |||
JHHLHNBC_01960 | 8.1e-151 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
JHHLHNBC_01961 | 1.1e-17 | |||||
JHHLHNBC_01962 | 2.8e-44 | |||||
JHHLHNBC_01963 | 2.6e-146 | S | haloacid dehalogenase-like hydrolase | |||
JHHLHNBC_01964 | 4e-130 | 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 | |
JHHLHNBC_01965 | 1.1e-210 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_01966 | 2.6e-191 | K | sequence-specific DNA binding | |||
JHHLHNBC_01967 | 2.5e-150 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_01968 | 3e-159 | K | sequence-specific DNA binding | |||
JHHLHNBC_01969 | 2.9e-45 | XK27_07075 | S | CAAX protease self-immunity | ||
JHHLHNBC_01970 | 4e-54 | |||||
JHHLHNBC_01971 | 1.3e-42 | |||||
JHHLHNBC_01972 | 5.7e-277 | pipD | E | Dipeptidase | ||
JHHLHNBC_01973 | 2.3e-81 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
JHHLHNBC_01974 | 2.3e-68 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_01975 | 2.6e-82 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_01976 | 1e-119 | 3.6.1.27 | I | Acid phosphatase homologues | ||
JHHLHNBC_01977 | 1.2e-113 | S | Domain of unknown function (DUF4811) | |||
JHHLHNBC_01978 | 8.1e-266 | lmrB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_01979 | 1.5e-80 | merR | K | MerR HTH family regulatory protein | ||
JHHLHNBC_01980 | 7.2e-68 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
JHHLHNBC_01981 | 1.1e-107 | XK27_02070 | S | Nitroreductase family | ||
JHHLHNBC_01982 | 9.6e-138 | 4.1.2.14 | S | KDGP aldolase | ||
JHHLHNBC_01983 | 9.1e-206 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
JHHLHNBC_01984 | 2e-216 | dho | 3.5.2.3 | S | Amidohydrolase family | |
JHHLHNBC_01985 | 3.6e-107 | S | Domain of unknown function (DUF4310) | |||
JHHLHNBC_01986 | 1.7e-137 | S | Domain of unknown function (DUF4311) | |||
JHHLHNBC_01987 | 6e-53 | S | Domain of unknown function (DUF4312) | |||
JHHLHNBC_01988 | 1.2e-61 | S | Glycine-rich SFCGS | |||
JHHLHNBC_01989 | 3.6e-55 | S | PRD domain | |||
JHHLHNBC_01990 | 0.0 | K | Mga helix-turn-helix domain | |||
JHHLHNBC_01991 | 4.5e-123 | tal | 2.2.1.2 | H | Pfam:Transaldolase | |
JHHLHNBC_01992 | 4.1e-65 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
JHHLHNBC_01993 | 1.1e-195 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
JHHLHNBC_01994 | 2.2e-102 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
JHHLHNBC_01995 | 1.2e-88 | gutM | K | Glucitol operon activator protein (GutM) | ||
JHHLHNBC_01996 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
JHHLHNBC_01997 | 2.2e-145 | IQ | NAD dependent epimerase/dehydratase family | |||
JHHLHNBC_01998 | 3.8e-204 | yloV | S | DAK2 domain fusion protein YloV | ||
JHHLHNBC_01999 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
JHHLHNBC_02000 | 1e-187 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
JHHLHNBC_02001 | 8.9e-37 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
JHHLHNBC_02002 | 2.2e-193 | oppD | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_02003 | 1.2e-85 | 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 | ||
JHHLHNBC_02004 | 2.7e-296 | 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 | |
JHHLHNBC_02005 | 4.5e-188 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
JHHLHNBC_02006 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
JHHLHNBC_02007 | 4.5e-38 | nrdH | O | Glutaredoxin | ||
JHHLHNBC_02008 | 4e-53 | yrzB | S | Belongs to the UPF0473 family | ||
JHHLHNBC_02010 | 3.4e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
JHHLHNBC_02011 | 1.6e-91 | cvpA | S | Colicin V production protein | ||
JHHLHNBC_02012 | 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 | ||
JHHLHNBC_02013 | 4.7e-215 | 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 | |
JHHLHNBC_02014 | 5.5e-30 | |||||
JHHLHNBC_02015 | 7.9e-07 | |||||
JHHLHNBC_02016 | 4.4e-61 | V | ABC transporter | |||
JHHLHNBC_02018 | 4.6e-123 | S | GDSL-like Lipase/Acylhydrolase family | |||
JHHLHNBC_02019 | 1.3e-296 | G | MFS/sugar transport protein | |||
JHHLHNBC_02020 | 0.0 | S | Glycosyl hydrolase family 115 | |||
JHHLHNBC_02021 | 2.8e-09 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
JHHLHNBC_02022 | 4.3e-66 | cadA | P | P-type ATPase | ||
JHHLHNBC_02023 | 3.6e-244 | cadA | P | P-type ATPase | ||
JHHLHNBC_02024 | 1.2e-79 | hsp3 | O | Hsp20/alpha crystallin family | ||
JHHLHNBC_02025 | 2.4e-71 | S | Iron-sulphur cluster biosynthesis | |||
JHHLHNBC_02026 | 4.3e-218 | htrA | 3.4.21.107 | O | serine protease | |
JHHLHNBC_02027 | 6e-154 | vicX | 3.1.26.11 | S | domain protein | |
JHHLHNBC_02028 | 9.7e-141 | yycI | S | YycH protein | ||
JHHLHNBC_02029 | 1.5e-245 | yycH | S | YycH protein | ||
JHHLHNBC_02030 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_02031 | 3.1e-130 | K | response regulator | |||
JHHLHNBC_02032 | 5.7e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_02033 | 3e-190 | oppD | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_02034 | 3.9e-171 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
JHHLHNBC_02035 | 7.3e-156 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
JHHLHNBC_02036 | 8.3e-256 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_02037 | 8.5e-277 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_02038 | 6.4e-207 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_02039 | 2.2e-99 | 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 | ||
JHHLHNBC_02040 | 3.4e-161 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
JHHLHNBC_02041 | 5.2e-156 | pstS | P | Phosphate | ||
JHHLHNBC_02042 | 1.2e-305 | phoR | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_02043 | 3.4e-129 | K | response regulator | |||
JHHLHNBC_02044 | 2.8e-163 | XK27_00670 | S | ABC transporter | ||
JHHLHNBC_02045 | 0.0 | bglB | 3.2.1.21 | GH3 | G | hydrolase, family 3 |
JHHLHNBC_02046 | 3.4e-152 | rrmA | 2.1.1.187 | H | Methyltransferase | |
JHHLHNBC_02047 | 1.3e-155 | corA | P | CorA-like Mg2+ transporter protein | ||
JHHLHNBC_02048 | 0.0 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
JHHLHNBC_02049 | 1.7e-51 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
JHHLHNBC_02050 | 3.7e-123 | azlC | E | branched-chain amino acid | ||
JHHLHNBC_02052 | 1.1e-105 | S | Membrane | |||
JHHLHNBC_02053 | 1.4e-283 | pipD | E | Dipeptidase | ||
JHHLHNBC_02054 | 0.0 | V | ABC transporter | |||
JHHLHNBC_02055 | 3.3e-306 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_02056 | 3.1e-115 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
JHHLHNBC_02057 | 1.5e-242 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
JHHLHNBC_02058 | 6.9e-113 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_02059 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
JHHLHNBC_02060 | 1e-60 | glnR | K | Transcriptional regulator | ||
JHHLHNBC_02061 | 3.2e-158 | ylbM | S | Belongs to the UPF0348 family | ||
JHHLHNBC_02062 | 1.6e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
JHHLHNBC_02064 | 4.6e-17 | yhcX | S | Psort location Cytoplasmic, score | ||
JHHLHNBC_02065 | 2.2e-237 | L | Probable transposase | |||
JHHLHNBC_02066 | 1.5e-140 | M | Peptidase family M23 | |||
JHHLHNBC_02067 | 7.2e-272 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
JHHLHNBC_02068 | 7.9e-123 | K | response regulator | |||
JHHLHNBC_02069 | 1.1e-289 | arlS | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_02070 | 4.5e-180 | 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 | ||
JHHLHNBC_02071 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
JHHLHNBC_02072 | 1.9e-239 | G | Bacterial extracellular solute-binding protein | |||
JHHLHNBC_02074 | 2.5e-78 | |||||
JHHLHNBC_02075 | 1.1e-295 | strH | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain |
JHHLHNBC_02076 | 0.0 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_02077 | 1.5e-77 | frvA | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_02078 | 3.7e-255 | manP | 2.7.1.191, 2.7.1.202 | G | phosphotransferase system | |
JHHLHNBC_02079 | 9.9e-196 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
JHHLHNBC_02080 | 7.7e-129 | XK27_08435 | K | UTRA | ||
JHHLHNBC_02081 | 2e-219 | agaS | G | SIS domain | ||
JHHLHNBC_02082 | 7.6e-227 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
JHHLHNBC_02083 | 0.0 | bgaC | 3.2.1.23 | G | Glycosyl hydrolases family 35 | |
JHHLHNBC_02084 | 4.7e-82 | manX_1 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_02085 | 4.8e-160 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
JHHLHNBC_02086 | 4.2e-147 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
JHHLHNBC_02087 | 1.2e-64 | XK27_08465 | 2.7.1.191 | G | PTS system fructose IIA component | |
JHHLHNBC_02088 | 2.7e-214 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
JHHLHNBC_02089 | 1e-226 | 4.4.1.8 | E | Aminotransferase, class I | ||
JHHLHNBC_02090 | 1.8e-198 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
JHHLHNBC_02091 | 1.1e-250 | U | 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 | |||
JHHLHNBC_02092 | 5.7e-58 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_02093 | 2.7e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
JHHLHNBC_02094 | 3.2e-192 | ypdE | E | M42 glutamyl aminopeptidase | ||
JHHLHNBC_02095 | 6.7e-307 | 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_02096 | 6e-238 | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | ||
JHHLHNBC_02097 | 8e-299 | E | ABC transporter, substratebinding protein | |||
JHHLHNBC_02098 | 3.2e-166 | gmuE | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
JHHLHNBC_02099 | 0.0 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
JHHLHNBC_02100 | 8.8e-206 | S | Calcineurin-like phosphoesterase | |||
JHHLHNBC_02101 | 8.8e-162 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
JHHLHNBC_02102 | 5.1e-176 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JHHLHNBC_02103 | 1.3e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
JHHLHNBC_02104 | 1.3e-165 | natA | S | ABC transporter | ||
JHHLHNBC_02105 | 3.2e-210 | ysdA | CP | ABC-2 family transporter protein | ||
JHHLHNBC_02106 | 2.4e-63 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
JHHLHNBC_02107 | 2.4e-161 | CcmA | V | ABC transporter | ||
JHHLHNBC_02108 | 7.4e-115 | VPA0052 | I | ABC-2 family transporter protein | ||
JHHLHNBC_02109 | 1.4e-144 | IQ | reductase | |||
JHHLHNBC_02110 | 3.9e-257 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JHHLHNBC_02111 | 0.0 | bglP | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_02112 | 1.7e-159 | licT | K | CAT RNA binding domain | ||
JHHLHNBC_02113 | 2.2e-288 | cydC | V | ABC transporter transmembrane region | ||
JHHLHNBC_02114 | 3.5e-310 | cydD | CO | ABC transporter transmembrane region | ||
JHHLHNBC_02115 | 4.9e-75 | ynhH | S | NusG domain II | ||
JHHLHNBC_02116 | 2.4e-174 | M | Peptidoglycan-binding domain 1 protein | |||
JHHLHNBC_02117 | 8e-37 | XK27_02675 | K | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_02118 | 5.1e-114 | S | CRISPR-associated protein (Cas_Csn2) | |||
JHHLHNBC_02119 | 4.8e-48 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
JHHLHNBC_02120 | 2.3e-168 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
JHHLHNBC_02121 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
JHHLHNBC_02122 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
JHHLHNBC_02123 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
JHHLHNBC_02124 | 5e-182 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
JHHLHNBC_02125 | 7.1e-80 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
JHHLHNBC_02126 | 5.7e-172 | whiA | K | May be required for sporulation | ||
JHHLHNBC_02127 | 5.9e-191 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
JHHLHNBC_02128 | 1.7e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
JHHLHNBC_02129 | 8.7e-85 | S | Short repeat of unknown function (DUF308) | |||
JHHLHNBC_02130 | 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 | ||
JHHLHNBC_02131 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
JHHLHNBC_02132 | 1.9e-118 | yfbR | S | HD containing hydrolase-like enzyme | ||
JHHLHNBC_02133 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
JHHLHNBC_02134 | 2.2e-257 | yhdP | S | Transporter associated domain | ||
JHHLHNBC_02135 | 3.8e-145 | S | Alpha beta hydrolase | |||
JHHLHNBC_02136 | 1.4e-203 | G | Acyltransferase family | |||
JHHLHNBC_02137 | 1e-260 | lmrB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02138 | 7.4e-86 | S | Domain of unknown function (DUF4811) | |||
JHHLHNBC_02139 | 3.5e-97 | maf | D | nucleoside-triphosphate diphosphatase activity | ||
JHHLHNBC_02140 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
JHHLHNBC_02141 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
JHHLHNBC_02142 | 0.0 | ydaO | E | amino acid | ||
JHHLHNBC_02143 | 7.1e-43 | |||||
JHHLHNBC_02144 | 6.8e-116 | pacL | 3.6.3.8 | P | P-type ATPase | |
JHHLHNBC_02145 | 2.1e-76 | marR | K | Winged helix DNA-binding domain | ||
JHHLHNBC_02146 | 5.3e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
JHHLHNBC_02147 | 2.1e-76 | marR | K | Winged helix DNA-binding domain | ||
JHHLHNBC_02148 | 9e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
JHHLHNBC_02150 | 1.2e-82 | yslB | S | Protein of unknown function (DUF2507) | ||
JHHLHNBC_02151 | 1.1e-59 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_02152 | 1.8e-133 | lys | M | Glycosyl hydrolases family 25 | ||
JHHLHNBC_02153 | 3.2e-29 | |||||
JHHLHNBC_02154 | 5e-120 | qmcA | O | prohibitin homologues | ||
JHHLHNBC_02155 | 6.2e-165 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
JHHLHNBC_02156 | 4.5e-74 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_02157 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
JHHLHNBC_02158 | 1.5e-163 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
JHHLHNBC_02159 | 3.3e-144 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_02160 | 2.5e-217 | yttB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02161 | 0.0 | res | 2.1.1.72, 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
JHHLHNBC_02162 | 1.6e-154 | mod | 2.1.1.72 | L | DNA methylase | |
JHHLHNBC_02164 | 8.2e-25 | |||||
JHHLHNBC_02165 | 4.2e-95 | sigH | K | Sigma-70 region 2 | ||
JHHLHNBC_02166 | 1e-301 | ybeC | E | amino acid | ||
JHHLHNBC_02167 | 4.4e-46 | rbsA | 3.6.3.17 | G | ABC transporter | |
JHHLHNBC_02168 | 1e-152 | rbsC | U | Belongs to the binding-protein-dependent transport system permease family | ||
JHHLHNBC_02169 | 8e-158 | rbsB | G | Periplasmic binding protein domain | ||
JHHLHNBC_02170 | 9.6e-164 | 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 | |
JHHLHNBC_02171 | 2e-38 | K | DNA-binding helix-turn-helix protein | |||
JHHLHNBC_02172 | 1.6e-277 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
JHHLHNBC_02173 | 3.4e-226 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_02174 | 1e-111 | |||||
JHHLHNBC_02175 | 1.1e-40 | |||||
JHHLHNBC_02176 | 1.1e-206 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
JHHLHNBC_02177 | 2.5e-42 | |||||
JHHLHNBC_02178 | 5.8e-213 | mccF | V | LD-carboxypeptidase | ||
JHHLHNBC_02179 | 2.1e-182 | yveB | 2.7.4.29 | I | PAP2 superfamily | |
JHHLHNBC_02180 | 2.8e-171 | L | Transposase | |||
JHHLHNBC_02181 | 1.1e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
JHHLHNBC_02182 | 1.5e-91 | yhbO | 3.5.1.124 | S | DJ-1/PfpI family | |
JHHLHNBC_02183 | 3.4e-280 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
JHHLHNBC_02184 | 3.8e-182 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
JHHLHNBC_02185 | 2.1e-28 | |||||
JHHLHNBC_02186 | 2.6e-222 | 2.4.1.9, 3.4.24.40 | GH68 | S | peptidase inhibitor activity | |
JHHLHNBC_02187 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
JHHLHNBC_02188 | 1.1e-166 | arbZ | I | Phosphate acyltransferases | ||
JHHLHNBC_02189 | 2.6e-180 | arbY | M | family 8 | ||
JHHLHNBC_02190 | 3.3e-163 | arbx | M | Glycosyl transferase family 8 | ||
JHHLHNBC_02191 | 1.2e-143 | arbV | 2.3.1.51 | I | Phosphate acyltransferases | |
JHHLHNBC_02192 | 1.2e-247 | cycA | E | Amino acid permease | ||
JHHLHNBC_02193 | 3.8e-73 | |||||
JHHLHNBC_02194 | 8.2e-185 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
JHHLHNBC_02195 | 3.7e-46 | |||||
JHHLHNBC_02196 | 6.4e-76 | |||||
JHHLHNBC_02197 | 7.9e-52 | |||||
JHHLHNBC_02199 | 5.1e-48 | |||||
JHHLHNBC_02200 | 6.8e-165 | comGB | NU | type II secretion system | ||
JHHLHNBC_02201 | 2.1e-133 | comGA | NU | Type II IV secretion system protein | ||
JHHLHNBC_02202 | 9.3e-101 | yebC | K | Transcriptional regulatory protein | ||
JHHLHNBC_02203 | 3.4e-215 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
JHHLHNBC_02204 | 3.8e-232 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
JHHLHNBC_02205 | 1.4e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
JHHLHNBC_02206 | 3.5e-48 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
JHHLHNBC_02207 | 2.9e-20 | |||||
JHHLHNBC_02208 | 5.3e-21 | L | PFAM Integrase core domain | |||
JHHLHNBC_02209 | 2.5e-86 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
JHHLHNBC_02211 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
JHHLHNBC_02212 | 8.9e-176 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
JHHLHNBC_02213 | 1.9e-124 | ftsE | D | ABC transporter | ||
JHHLHNBC_02214 | 1.8e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
JHHLHNBC_02215 | 2.5e-195 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
JHHLHNBC_02216 | 5.2e-145 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
JHHLHNBC_02217 | 2e-225 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
JHHLHNBC_02219 | 3e-213 | pimH | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02220 | 1.2e-36 | |||||
JHHLHNBC_02221 | 3.3e-32 | |||||
JHHLHNBC_02222 | 3.2e-08 | |||||
JHHLHNBC_02223 | 4.5e-102 | KT | Purine catabolism regulatory protein-like family | |||
JHHLHNBC_02224 | 1.1e-175 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_02225 | 5.3e-117 | udp | 2.4.2.3, 3.2.2.4 | F | Phosphorylase superfamily | |
JHHLHNBC_02226 | 4.1e-191 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_02227 | 1.6e-155 | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | ||
JHHLHNBC_02229 | 3.3e-195 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
JHHLHNBC_02230 | 2.1e-45 | |||||
JHHLHNBC_02231 | 9.2e-198 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
JHHLHNBC_02232 | 3.1e-124 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
JHHLHNBC_02233 | 6.9e-93 | ccpN | K | Domain in cystathionine beta-synthase and other proteins. | ||
JHHLHNBC_02234 | 0.0 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
JHHLHNBC_02235 | 0.0 | kup | P | Transport of potassium into the cell | ||
JHHLHNBC_02236 | 2.1e-165 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_02237 | 8.6e-202 | S | ABC-2 family transporter protein | |||
JHHLHNBC_02238 | 1.2e-197 | |||||
JHHLHNBC_02239 | 2.9e-18 | |||||
JHHLHNBC_02240 | 1.5e-35 | chpA | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
JHHLHNBC_02241 | 1.7e-259 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
JHHLHNBC_02242 | 1.7e-251 | pepC | 3.4.22.40 | E | aminopeptidase | |
JHHLHNBC_02243 | 2.9e-50 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
JHHLHNBC_02244 | 3.3e-100 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
JHHLHNBC_02245 | 1e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
JHHLHNBC_02246 | 6.2e-214 | 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) | |
JHHLHNBC_02247 | 3e-303 | frvR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_02248 | 1.1e-121 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_02249 | 1.5e-132 | G | Phosphoglycerate mutase family | |||
JHHLHNBC_02250 | 8.7e-09 | |||||
JHHLHNBC_02251 | 5.7e-116 | ymfM | S | Helix-turn-helix domain | ||
JHHLHNBC_02252 | 1.6e-103 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
JHHLHNBC_02253 | 3.1e-226 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
JHHLHNBC_02254 | 1.9e-189 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
JHHLHNBC_02255 | 4.9e-31 | ykzG | S | Belongs to the UPF0356 family | ||
JHHLHNBC_02256 | 2.8e-260 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
JHHLHNBC_02257 | 6.9e-150 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
JHHLHNBC_02258 | 3.8e-142 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
JHHLHNBC_02259 | 9.4e-233 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
JHHLHNBC_02260 | 1.3e-154 | azoB | GM | NmrA-like family | ||
JHHLHNBC_02262 | 3.5e-301 | scrB | 3.2.1.26 | GH32 | G | invertase |
JHHLHNBC_02263 | 1.2e-177 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
JHHLHNBC_02264 | 0.0 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
JHHLHNBC_02265 | 2.6e-166 | malG | P | ABC-type sugar transport systems, permease components | ||
JHHLHNBC_02266 | 7.7e-149 | malK | P | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_02267 | 1.1e-86 | ypmB | S | Protein conserved in bacteria | ||
JHHLHNBC_02268 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
JHHLHNBC_02269 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
JHHLHNBC_02270 | 4.9e-168 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
JHHLHNBC_02271 | 1.8e-206 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
JHHLHNBC_02272 | 1.9e-121 | drgA | C | Nitroreductase family | ||
JHHLHNBC_02273 | 6.8e-68 | yqkB | S | Belongs to the HesB IscA family | ||
JHHLHNBC_02274 | 5.1e-240 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
JHHLHNBC_02275 | 4.4e-121 | K | cheY-homologous receiver domain | |||
JHHLHNBC_02276 | 9.2e-71 | S | GtrA-like protein | |||
JHHLHNBC_02277 | 0.0 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
JHHLHNBC_02278 | 1.5e-180 | ykcC | GT2 | M | Glycosyl transferase family 2 | |
JHHLHNBC_02279 | 0.0 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
JHHLHNBC_02280 | 9.1e-178 | yhfP | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
JHHLHNBC_02281 | 1.8e-142 | cmpC | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_02282 | 1.5e-159 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
JHHLHNBC_02283 | 7.6e-164 | XK27_00670 | S | ABC transporter | ||
JHHLHNBC_02284 | 6.6e-81 | yodP | 2.3.1.264 | K | FR47-like protein | |
JHHLHNBC_02285 | 6.2e-84 | ydcK | S | Belongs to the SprT family | ||
JHHLHNBC_02286 | 5e-131 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_02287 | 1.1e-129 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
JHHLHNBC_02288 | 2.3e-176 | XK27_08835 | S | ABC transporter | ||
JHHLHNBC_02289 | 1.3e-73 | |||||
JHHLHNBC_02290 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
JHHLHNBC_02291 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
JHHLHNBC_02292 | 1.5e-74 | argR | K | Regulates arginine biosynthesis genes | ||
JHHLHNBC_02293 | 2.9e-151 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_02294 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
JHHLHNBC_02295 | 4.6e-55 | yheA | S | Control of competence regulator ComK, YlbF/YmcA | ||
JHHLHNBC_02296 | 2.1e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
JHHLHNBC_02297 | 5.4e-71 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
JHHLHNBC_02298 | 1.6e-263 | G | MFS/sugar transport protein | |||
JHHLHNBC_02299 | 5.4e-74 | S | function, without similarity to other proteins | |||
JHHLHNBC_02300 | 1.4e-65 | |||||
JHHLHNBC_02301 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_02302 | 3e-257 | dtpT | U | amino acid peptide transporter | ||
JHHLHNBC_02303 | 7.5e-160 | yjjH | S | Calcineurin-like phosphoesterase | ||
JHHLHNBC_02304 | 2.3e-181 | bioH | 2.1.1.197, 3.1.1.85, 3.7.1.13, 3.7.1.9, 4.2.99.20 | E | Alpha/beta hydrolase family | |
JHHLHNBC_02305 | 5.2e-231 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
JHHLHNBC_02306 | 1.9e-62 | P | Rhodanese-like domain | |||
JHHLHNBC_02307 | 4e-84 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
JHHLHNBC_02308 | 1.8e-66 | K | MarR family | |||
JHHLHNBC_02309 | 3.1e-11 | S | response to antibiotic | |||
JHHLHNBC_02310 | 8.5e-172 | |||||
JHHLHNBC_02311 | 4.9e-09 | S | response to antibiotic | |||
JHHLHNBC_02312 | 2.9e-102 | rmaB | K | Iron dependent repressor, N-terminal DNA binding domain | ||
JHHLHNBC_02313 | 3.8e-84 | F | NUDIX domain | |||
JHHLHNBC_02314 | 3e-230 | U | Major Facilitator Superfamily | |||
JHHLHNBC_02315 | 2.8e-45 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
JHHLHNBC_02316 | 1.8e-130 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
JHHLHNBC_02317 | 3.5e-177 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
JHHLHNBC_02318 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
JHHLHNBC_02319 | 2.5e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
JHHLHNBC_02320 | 6.9e-164 | cvfB | S | S1 domain | ||
JHHLHNBC_02321 | 3.3e-166 | xerD | D | recombinase XerD | ||
JHHLHNBC_02322 | 2.7e-177 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
JHHLHNBC_02323 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
JHHLHNBC_02324 | 7.2e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
JHHLHNBC_02325 | 9e-164 | cvfB | S | S1 domain | ||
JHHLHNBC_02326 | 4.8e-141 | xerD | D | recombinase XerD | ||
JHHLHNBC_02327 | 9.6e-239 | malE | G | Bacterial extracellular solute-binding protein | ||
JHHLHNBC_02328 | 1.7e-82 | |||||
JHHLHNBC_02329 | 3.7e-195 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
JHHLHNBC_02330 | 9e-130 | XK27_08435 | K | UTRA | ||
JHHLHNBC_02331 | 5.9e-219 | agaS | G | SIS domain | ||
JHHLHNBC_02332 | 4.1e-225 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
JHHLHNBC_02333 | 0.0 | bgaC | 3.2.1.23 | G | Glycosyl hydrolases family 35 | |
JHHLHNBC_02334 | 8.1e-82 | manX_1 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_02335 | 1.5e-140 | XK27_08455 | G | PTS system sorbose-specific iic component | ||
JHHLHNBC_02336 | 1.5e-144 | manZ_1 | G | PTS system mannose/fructose/sorbose family IID component | ||
JHHLHNBC_02337 | 7.8e-64 | XK27_08465 | 2.7.1.191 | G | PTS system fructose IIA component | |
JHHLHNBC_02338 | 1e-173 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | F | pfkB family carbohydrate kinase | |
JHHLHNBC_02339 | 5.4e-147 | IQ | KR domain | |||
JHHLHNBC_02340 | 6.1e-244 | gatC | G | PTS system sugar-specific permease component | ||
JHHLHNBC_02341 | 6.2e-85 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_02342 | 1.5e-46 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_02343 | 2.8e-162 | |||||
JHHLHNBC_02344 | 1.3e-41 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
JHHLHNBC_02345 | 2.2e-229 | 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) | |
JHHLHNBC_02346 | 8.2e-37 | cspA | K | Cold shock protein | ||
JHHLHNBC_02347 | 1.5e-145 | pstS | P | Phosphate | ||
JHHLHNBC_02348 | 8.1e-263 | ydiC1 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02349 | 6.2e-208 | yaaN | P | Toxic anion resistance protein (TelA) | ||
JHHLHNBC_02350 | 6.9e-116 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
JHHLHNBC_02351 | 1.9e-223 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
JHHLHNBC_02352 | 4.8e-227 | 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 | ||
JHHLHNBC_02353 | 8.8e-70 | 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 | ||
JHHLHNBC_02354 | 4.7e-45 | yggT | D | integral membrane protein | ||
JHHLHNBC_02355 | 3e-147 | ylmH | S | S4 domain protein | ||
JHHLHNBC_02356 | 3.2e-80 | divIVA | D | DivIVA protein | ||
JHHLHNBC_02357 | 5.1e-105 | mntB | 3.6.3.35 | P | ABC transporter | |
JHHLHNBC_02358 | 9.5e-145 | mtsB | U | ABC 3 transport family | ||
JHHLHNBC_02359 | 5.4e-175 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_02360 | 8.7e-51 | czrA | K | Transcriptional regulator, ArsR family | ||
JHHLHNBC_02361 | 1.1e-104 | 2.5.1.105 | P | Cation efflux family | ||
JHHLHNBC_02362 | 1e-24 | |||||
JHHLHNBC_02363 | 3.6e-309 | mco | Q | Multicopper oxidase | ||
JHHLHNBC_02364 | 6e-239 | EGP | Major Facilitator Superfamily | |||
JHHLHNBC_02365 | 9.8e-64 | |||||
JHHLHNBC_02366 | 0.0 | pacL | P | P-type ATPase | ||
JHHLHNBC_02367 | 5.3e-279 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
JHHLHNBC_02368 | 2.3e-18 | |||||
JHHLHNBC_02369 | 2.4e-128 | |||||
JHHLHNBC_02370 | 2.3e-237 | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | ||
JHHLHNBC_02371 | 3.2e-292 | E | ABC transporter, substratebinding protein | |||
JHHLHNBC_02372 | 4.5e-120 | S | Acetyltransferase (GNAT) family | |||
JHHLHNBC_02374 | 3e-125 | nisT | V | ABC transporter | ||
JHHLHNBC_02375 | 3.4e-170 | nisT | V | ABC transporter | ||
JHHLHNBC_02376 | 8.3e-94 | S | ABC-type cobalt transport system, permease component | |||
JHHLHNBC_02377 | 1.3e-243 | P | ABC transporter | |||
JHHLHNBC_02378 | 1.1e-158 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
JHHLHNBC_02379 | 4.7e-143 | 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 | ||
JHHLHNBC_02380 | 3.6e-137 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
JHHLHNBC_02381 | 6.5e-75 | K | TipAS antibiotic-recognition domain | |||
JHHLHNBC_02382 | 1.1e-33 | |||||
JHHLHNBC_02383 | 7.6e-129 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
JHHLHNBC_02384 | 1e-185 | yxeA | V | FtsX-like permease family | ||
JHHLHNBC_02385 | 2.5e-104 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_02386 | 0.0 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
JHHLHNBC_02387 | 3.1e-235 | mesE | M | Transport protein ComB | ||
JHHLHNBC_02388 | 1.8e-175 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
JHHLHNBC_02389 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
JHHLHNBC_02390 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
JHHLHNBC_02392 | 3.4e-118 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_02393 | 7.6e-85 | F | NUDIX domain | |||
JHHLHNBC_02394 | 6.1e-175 | U | Major Facilitator Superfamily | |||
JHHLHNBC_02395 | 4.9e-37 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
JHHLHNBC_02396 | 3.5e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
JHHLHNBC_02397 | 6.9e-150 | 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 | |
JHHLHNBC_02398 | 3.7e-157 | pstA | P | Phosphate transport system permease protein PstA | ||
JHHLHNBC_02399 | 8.6e-157 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
JHHLHNBC_02400 | 8e-157 | pstS | P | Phosphate | ||
JHHLHNBC_02401 | 7.3e-308 | phoR | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_02402 | 3.1e-130 | K | response regulator | |||
JHHLHNBC_02403 | 9.3e-69 | psiE | S | Phosphate-starvation-inducible E | ||
JHHLHNBC_02404 | 3.3e-288 | |||||
JHHLHNBC_02405 | 2.7e-105 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
JHHLHNBC_02406 | 6.9e-203 | yfjR | K | WYL domain | ||
JHHLHNBC_02407 | 2.4e-150 | S | Fic/DOC family | |||
JHHLHNBC_02408 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
JHHLHNBC_02410 | 1.5e-172 | |||||
JHHLHNBC_02411 | 1.9e-250 | 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 | |
JHHLHNBC_02412 | 9.7e-180 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
JHHLHNBC_02413 | 5.2e-240 | ytoI | K | DRTGG domain | ||
JHHLHNBC_02414 | 1.8e-164 | 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 | |
JHHLHNBC_02415 | 1.5e-214 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
JHHLHNBC_02416 | 5.4e-110 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
JHHLHNBC_02417 | 1.8e-229 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
JHHLHNBC_02418 | 4.1e-104 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
JHHLHNBC_02419 | 2.6e-112 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
JHHLHNBC_02420 | 1.1e-133 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
JHHLHNBC_02421 | 4.3e-130 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
JHHLHNBC_02422 | 2.4e-53 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
JHHLHNBC_02423 | 1.3e-51 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
JHHLHNBC_02424 | 2.5e-195 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
JHHLHNBC_02425 | 1e-142 | Q | Fumarylacetoacetate (FAA) hydrolase family | |||
JHHLHNBC_02426 | 3.2e-110 | nfnB | 1.5.1.34 | C | Nitroreductase family | |
JHHLHNBC_02427 | 2.8e-214 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_02428 | 4.1e-127 | T | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_02429 | 2.6e-172 | T | PhoQ Sensor | |||
JHHLHNBC_02430 | 4.7e-132 | XK27_05695 | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_02431 | 0.0 | ysaB | V | FtsX-like permease family | ||
JHHLHNBC_02432 | 4.1e-59 | |||||
JHHLHNBC_02433 | 3.9e-204 | xerS | L | Belongs to the 'phage' integrase family | ||
JHHLHNBC_02434 | 5.2e-170 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
JHHLHNBC_02435 | 4.7e-182 | K | LysR substrate binding domain | |||
JHHLHNBC_02436 | 1.9e-171 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
JHHLHNBC_02437 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
JHHLHNBC_02438 | 3e-148 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
JHHLHNBC_02439 | 1e-195 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
JHHLHNBC_02440 | 1.6e-174 | |||||
JHHLHNBC_02441 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
JHHLHNBC_02442 | 9.4e-17 | |||||
JHHLHNBC_02443 | 3.7e-102 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_02444 | 9.6e-59 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
JHHLHNBC_02445 | 1.1e-98 | dhaL | 2.7.1.121 | S | Dak2 | |
JHHLHNBC_02446 | 3.9e-173 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
JHHLHNBC_02447 | 1.3e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
JHHLHNBC_02448 | 5.3e-198 | 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) |
JHHLHNBC_02449 | 6e-263 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
JHHLHNBC_02450 | 9.2e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
JHHLHNBC_02451 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
JHHLHNBC_02452 | 6.2e-58 | ftsL | D | cell division protein FtsL | ||
JHHLHNBC_02453 | 1.8e-170 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
JHHLHNBC_02454 | 4.8e-78 | mraZ | K | Belongs to the MraZ family | ||
JHHLHNBC_02455 | 1.2e-52 | |||||
JHHLHNBC_02457 | 2.2e-114 | L | PFAM transposase, IS4 family protein | |||
JHHLHNBC_02458 | 4.6e-56 | L | PFAM transposase, IS4 family protein | |||
JHHLHNBC_02459 | 8e-304 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
JHHLHNBC_02461 | 3.2e-50 | lciIC | K | Helix-turn-helix XRE-family like proteins | ||
JHHLHNBC_02463 | 7.7e-302 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
JHHLHNBC_02464 | 7.7e-252 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
JHHLHNBC_02465 | 1.2e-168 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
JHHLHNBC_02466 | 5.5e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
JHHLHNBC_02467 | 4.2e-256 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
JHHLHNBC_02468 | 9.6e-174 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
JHHLHNBC_02469 | 3.1e-110 | 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 | |
JHHLHNBC_02470 | 1.1e-83 | F | NUDIX domain | |||
JHHLHNBC_02471 | 1e-90 | S | AAA domain | |||
JHHLHNBC_02472 | 6.7e-113 | ycaC | Q | Isochorismatase family | ||
JHHLHNBC_02473 | 4.1e-259 | ydiC1 | EGP | Major Facilitator Superfamily | ||
JHHLHNBC_02474 | 2.9e-213 | yeaN | P | Transporter, major facilitator family protein | ||
JHHLHNBC_02475 | 2.9e-173 | iolS | C | Aldo keto reductase | ||
JHHLHNBC_02476 | 4.4e-64 | manO | S | Domain of unknown function (DUF956) | ||
JHHLHNBC_02477 | 5.2e-44 | yggT | D | integral membrane protein | ||
JHHLHNBC_02478 | 6.7e-78 | 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 | ||
JHHLHNBC_02479 | 3.1e-218 | 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 | ||
JHHLHNBC_02480 | 2e-217 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
JHHLHNBC_02481 | 1.4e-69 | tnp | L | DDE domain | ||
JHHLHNBC_02482 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
JHHLHNBC_02483 | 1.6e-177 | ccpA | K | catabolite control protein A | ||
JHHLHNBC_02484 | 3.7e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
JHHLHNBC_02485 | 4.6e-91 | niaR | S | 3H domain | ||
JHHLHNBC_02486 | 4.5e-83 | ytxH | S | YtxH-like protein | ||
JHHLHNBC_02487 | 2.8e-09 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
JHHLHNBC_02488 | 3.4e-155 | ykuT | M | mechanosensitive ion channel | ||
JHHLHNBC_02489 | 9.3e-156 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
JHHLHNBC_02490 | 4.6e-85 | ykuL | S | CBS domain | ||
JHHLHNBC_02491 | 1.6e-134 | gla | U | Major intrinsic protein | ||
JHHLHNBC_02492 | 2e-94 | S | Phosphoesterase | |||
JHHLHNBC_02493 | 2.6e-277 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
JHHLHNBC_02494 | 9.3e-68 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
JHHLHNBC_02495 | 3e-110 | XK27_02070 | S | Nitroreductase family | ||
JHHLHNBC_02496 | 1.4e-281 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
JHHLHNBC_02497 | 9.7e-55 | |||||
JHHLHNBC_02498 | 1.4e-270 | K | Mga helix-turn-helix domain | |||
JHHLHNBC_02499 | 1.3e-37 | nrdH | O | Glutaredoxin | ||
JHHLHNBC_02500 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
JHHLHNBC_02501 | 5.8e-188 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
JHHLHNBC_02502 | 8.5e-162 | K | Transcriptional regulator | |||
JHHLHNBC_02503 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
JHHLHNBC_02504 | 4.8e-193 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
JHHLHNBC_02505 | 5e-34 | |||||
JHHLHNBC_02506 | 1.1e-167 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
JHHLHNBC_02507 | 6.1e-221 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
JHHLHNBC_02508 | 1.3e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
JHHLHNBC_02511 | 1.5e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
JHHLHNBC_02512 | 1.7e-139 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
JHHLHNBC_02513 | 1e-97 | 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 | |
JHHLHNBC_02514 | 2.8e-85 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
JHHLHNBC_02515 | 1.6e-100 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
JHHLHNBC_02516 | 3.8e-57 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
JHHLHNBC_02517 | 7.7e-103 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
JHHLHNBC_02518 | 6.9e-192 | |||||
JHHLHNBC_02519 | 1.4e-152 | hutG | 3.5.3.8 | E | N-formylglutamate amidohydrolase | |
JHHLHNBC_02520 | 1.2e-54 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
JHHLHNBC_02521 | 3.7e-90 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
JHHLHNBC_02522 | 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 | |
JHHLHNBC_02523 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
JHHLHNBC_02524 | 7.1e-62 | |||||
JHHLHNBC_02525 | 2.5e-83 | 6.3.3.2 | S | ASCH | ||
JHHLHNBC_02526 | 1.6e-32 | |||||
JHHLHNBC_02527 | 8.6e-187 | 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 | ||
JHHLHNBC_02528 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
JHHLHNBC_02529 | 3.7e-246 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
JHHLHNBC_02530 | 1.9e-169 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
JHHLHNBC_02531 | 9.4e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
JHHLHNBC_02532 | 3.8e-257 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
JHHLHNBC_02533 | 1.3e-173 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
JHHLHNBC_02534 | 1.4e-102 | 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 | |
JHHLHNBC_02535 | 2.3e-240 | 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 | ||
JHHLHNBC_02536 | 1.5e-203 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
JHHLHNBC_02537 | 6.4e-31 | yaaA | S | S4 domain protein YaaA | ||
JHHLHNBC_02538 | 4.8e-202 | 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 | ||
JHHLHNBC_02539 | 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 | |
JHHLHNBC_02540 | 2.5e-231 | 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 | ||
JHHLHNBC_02541 | 2.3e-204 | 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 | |
JHHLHNBC_02542 | 1.2e-180 | K | sequence-specific DNA binding | |||
JHHLHNBC_02543 | 3.1e-56 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_02544 | 4e-42 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
JHHLHNBC_02545 | 6.6e-50 | |||||
JHHLHNBC_02546 | 2e-183 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
JHHLHNBC_02547 | 2.8e-55 | |||||
JHHLHNBC_02548 | 3.4e-80 | |||||
JHHLHNBC_02549 | 2.3e-207 | yubA | S | AI-2E family transporter | ||
JHHLHNBC_02550 | 5.8e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
JHHLHNBC_02551 | 6.6e-133 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_02552 | 2.6e-43 | |||||
JHHLHNBC_02553 | 5.3e-152 | V | Beta-lactamase | |||
JHHLHNBC_02554 | 1.6e-194 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
JHHLHNBC_02555 | 2.4e-141 | H | Protein of unknown function (DUF1698) | |||
JHHLHNBC_02557 | 5.7e-143 | puuD | S | peptidase C26 | ||
JHHLHNBC_02559 | 5.1e-259 | 6.3.1.2 | E | Glutamine synthetase N-terminal domain | ||
JHHLHNBC_02560 | 3.7e-226 | S | Amidohydrolase | |||
JHHLHNBC_02561 | 2.4e-248 | E | Amino acid permease | |||
JHHLHNBC_02563 | 1e-75 | K | helix_turn_helix, mercury resistance | |||
JHHLHNBC_02564 | 2.6e-163 | morA2 | S | reductase | ||
JHHLHNBC_02565 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1, 2.1.1.21 | E | GXGXG motif | |
JHHLHNBC_02566 | 7e-283 | gltD | 1.4.1.13, 1.4.1.14 | E | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
JHHLHNBC_02567 | 2.7e-131 | yciB | M | ErfK YbiS YcfS YnhG | ||
JHHLHNBC_02568 | 5.1e-119 | S | (CBS) domain | |||
JHHLHNBC_02569 | 6.8e-115 | 1.6.5.2 | S | Flavodoxin-like fold | ||
JHHLHNBC_02570 | 6.1e-250 | XK27_06930 | S | ABC-2 family transporter protein | ||
JHHLHNBC_02571 | 1.3e-96 | padR | K | Transcriptional regulator PadR-like family | ||
JHHLHNBC_02572 | 2e-263 | S | Putative peptidoglycan binding domain | |||
JHHLHNBC_02573 | 2.7e-126 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
JHHLHNBC_02575 | 2.6e-52 | trxC | O | Belongs to the thioredoxin family | ||
JHHLHNBC_02576 | 1.5e-138 | thrE | S | Putative threonine/serine exporter | ||
JHHLHNBC_02577 | 7e-75 | S | Threonine/Serine exporter, ThrE | |||
JHHLHNBC_02578 | 2.7e-211 | livJ | E | Receptor family ligand binding region | ||
JHHLHNBC_02579 | 3.1e-148 | livH | U | Branched-chain amino acid transport system / permease component | ||
JHHLHNBC_02580 | 1.5e-119 | livM | E | Branched-chain amino acid transport system / permease component | ||
JHHLHNBC_02581 | 3.6e-140 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
JHHLHNBC_02582 | 2.8e-123 | livF | E | ABC transporter | ||
JHHLHNBC_02583 | 1.1e-53 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
JHHLHNBC_02584 | 1.2e-168 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
JHHLHNBC_02585 | 2.9e-235 | 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 | ||
JHHLHNBC_02586 | 4.8e-117 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
JHHLHNBC_02587 | 5.2e-231 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
JHHLHNBC_02588 | 9.4e-127 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
JHHLHNBC_02589 | 6.5e-148 | M | NlpC P60 family protein | |||
JHHLHNBC_02590 | 3.6e-292 | lacE-1 | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | Phosphotransferase system, EIIC | |
JHHLHNBC_02591 | 5.4e-161 | K | CAT RNA binding domain | |||
JHHLHNBC_02592 | 3.3e-59 | lacF | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_02593 | 1.2e-234 | lacG | 3.2.1.85 | G | Belongs to the glycosyl hydrolase 1 family | |
JHHLHNBC_02594 | 3e-251 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
JHHLHNBC_02595 | 1.1e-133 | mod | 2.1.1.72, 3.1.21.5 | L | DNA methylase | |
JHHLHNBC_02596 | 1.2e-188 | cggR | K | Putative sugar-binding domain | ||
JHHLHNBC_02597 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
JHHLHNBC_02598 | 3.5e-152 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
JHHLHNBC_02599 | 5e-128 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
JHHLHNBC_02600 | 5.3e-113 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
JHHLHNBC_02601 | 1.5e-190 | pfoS | S | Phosphotransferase system, EIIC | ||
JHHLHNBC_02602 | 6.2e-51 | S | MazG-like family | |||
JHHLHNBC_02603 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
JHHLHNBC_02604 | 2.7e-42 | K | prlF antitoxin for toxin YhaV_toxin | |||
JHHLHNBC_02605 | 4.6e-160 | degV | S | EDD domain protein, DegV family | ||
JHHLHNBC_02606 | 1e-99 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
JHHLHNBC_02607 | 1.3e-204 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
JHHLHNBC_02608 | 9.2e-44 | 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) | |
JHHLHNBC_02609 | 2e-203 | camS | S | sex pheromone | ||
JHHLHNBC_02610 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
JHHLHNBC_02611 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
JHHLHNBC_02612 | 4.7e-46 | yjgN | S | Bacterial protein of unknown function (DUF898) | ||
JHHLHNBC_02613 | 2.6e-106 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
JHHLHNBC_02614 | 2.6e-174 | S | response to antibiotic | |||
JHHLHNBC_02616 | 1.6e-249 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
JHHLHNBC_02617 | 5.3e-59 | |||||
JHHLHNBC_02618 | 3.8e-82 | |||||
JHHLHNBC_02619 | 5.2e-72 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
JHHLHNBC_02620 | 7.6e-31 | |||||
JHHLHNBC_02621 | 9.5e-92 | yhbS | S | acetyltransferase | ||
JHHLHNBC_02622 | 7.1e-273 | yclK | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_02623 | 3.1e-133 | K | response regulator | |||
JHHLHNBC_02624 | 1.7e-69 | S | SdpI/YhfL protein family | |||
JHHLHNBC_02625 | 3.1e-71 | tnpB | L | Putative transposase DNA-binding domain | ||
JHHLHNBC_02626 | 1.2e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
JHHLHNBC_02627 | 1.7e-193 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
JHHLHNBC_02630 | 1.4e-86 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
JHHLHNBC_02631 | 2.2e-162 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
JHHLHNBC_02632 | 1.6e-143 | 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 | ||
JHHLHNBC_02633 | 5.5e-138 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
JHHLHNBC_02635 | 6.9e-136 | tipA | K | TipAS antibiotic-recognition domain | ||
JHHLHNBC_02636 | 6.4e-34 | |||||
JHHLHNBC_02637 | 6e-126 | devA | 3.6.3.25 | V | ATPases associated with a variety of cellular activities | |
JHHLHNBC_02638 | 9.4e-184 | yxeA | V | FtsX-like permease family | ||
JHHLHNBC_02639 | 2.1e-103 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_02644 | 1.2e-240 | L | PFAM Integrase core domain | |||
JHHLHNBC_02645 | 1.7e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
JHHLHNBC_02646 | 1.3e-243 | tilS | 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 | |
JHHLHNBC_02647 | 4.7e-82 | yabR | J | RNA binding | ||
JHHLHNBC_02648 | 4.4e-65 | divIC | D | cell cycle | ||
JHHLHNBC_02649 | 1.8e-38 | yabO | J | S4 domain protein | ||
JHHLHNBC_02650 | 4.7e-280 | yabM | S | Polysaccharide biosynthesis protein | ||
JHHLHNBC_02651 | 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 | ||
JHHLHNBC_02652 | 2.4e-101 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
JHHLHNBC_02653 | 1.2e-137 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
JHHLHNBC_02654 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
JHHLHNBC_02655 | 1e-207 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
JHHLHNBC_02656 | 1.2e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
JHHLHNBC_02657 | 3.8e-59 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
JHHLHNBC_02658 | 5e-53 | |||||
JHHLHNBC_02659 | 6.4e-87 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_02660 | 6.2e-78 | |||||
JHHLHNBC_02661 | 4.2e-60 | |||||
JHHLHNBC_02662 | 1.8e-91 | |||||
JHHLHNBC_02663 | 3e-238 | ydiC1 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02664 | 2.1e-68 | K | helix_turn_helix multiple antibiotic resistance protein | |||
JHHLHNBC_02665 | 1.5e-103 | |||||
JHHLHNBC_02666 | 3.5e-29 | |||||
JHHLHNBC_02667 | 4.7e-36 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_02668 | 1e-165 | GKT | transcriptional antiterminator | |||
JHHLHNBC_02669 | 2.1e-46 | ptxB | 2.7.1.194, 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_02670 | 1.4e-205 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
JHHLHNBC_02671 | 5.1e-48 | |||||
JHHLHNBC_02672 | 1.2e-149 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_02673 | 4.9e-87 | 6.3.4.4 | S | Zeta toxin | ||
JHHLHNBC_02674 | 7.3e-156 | rihB | 3.2.2.1 | F | Nucleoside | |
JHHLHNBC_02675 | 1.9e-211 | dcuD | C | Tripartite ATP-independent periplasmic transporter, DctM component | ||
JHHLHNBC_02676 | 5.3e-44 | K | Acetyltransferase (GNAT) family | |||
JHHLHNBC_02677 | 1.4e-117 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
JHHLHNBC_02678 | 1.7e-89 | 4.1.2.13 | G | DeoC/LacD family aldolase | ||
JHHLHNBC_02679 | 1.4e-37 | glpP | K | Regulates expression of the glpD operon. In the presence of glycerol 3-phosphate (G3P) causes antitermination of transcription of glpD at the inverted repeat of the leader region to enhance its transcription. Binds and stabilizes glpD leader mRNA | ||
JHHLHNBC_02680 | 1.4e-180 | 2.7.1.53 | G | Belongs to the FGGY kinase family | ||
JHHLHNBC_02681 | 1.8e-91 | IQ | KR domain | |||
JHHLHNBC_02682 | 8.5e-126 | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | ||
JHHLHNBC_02683 | 2e-139 | gatC | G | COG3775 Phosphotransferase system, galactitol-specific IIC component | ||
JHHLHNBC_02684 | 1e-286 | K | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
JHHLHNBC_02685 | 6.4e-154 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_02686 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | phosphotransferase system | |
JHHLHNBC_02687 | 5.4e-239 | sorE | E | Alcohol dehydrogenase GroES-like domain | ||
JHHLHNBC_02688 | 2.2e-163 | sorC | K | sugar-binding domain protein | ||
JHHLHNBC_02689 | 4.1e-131 | IQ | NAD dependent epimerase/dehydratase family | |||
JHHLHNBC_02690 | 3.6e-62 | sorF | 2.7.1.191, 2.7.1.206 | G | PTS system fructose IIA component | |
JHHLHNBC_02691 | 6.6e-79 | sorB | 2.7.1.191, 2.7.1.206 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_02692 | 7.3e-131 | sorA | U | PTS system sorbose-specific iic component | ||
JHHLHNBC_02693 | 1.2e-149 | sorM | G | system, mannose fructose sorbose family IID component | ||
JHHLHNBC_02694 | 4.9e-149 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_02695 | 1.1e-158 | salL | 2.5.1.63, 2.5.1.94 | K | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
JHHLHNBC_02696 | 3.5e-97 | S | UPF0397 protein | |||
JHHLHNBC_02697 | 0.0 | 3.6.3.24 | P | ATP-binding cassette cobalt transporter | ||
JHHLHNBC_02698 | 2.1e-146 | cbiQ | P | cobalt transport | ||
JHHLHNBC_02699 | 1.3e-150 | K | Transcriptional regulator, LacI family | |||
JHHLHNBC_02700 | 4.7e-244 | G | Major Facilitator | |||
JHHLHNBC_02701 | 4.3e-292 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
JHHLHNBC_02702 | 2.2e-250 | frdC | 1.3.5.4 | C | HI0933-like protein | |
JHHLHNBC_02703 | 2.9e-97 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
JHHLHNBC_02705 | 4.8e-188 | pts36C | G | iic component | ||
JHHLHNBC_02706 | 8.1e-09 | sgcB | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_02707 | 4.1e-30 | pts36A | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_02708 | 5.9e-63 | K | DeoR C terminal sensor domain | |||
JHHLHNBC_02709 | 9.2e-56 | lacC | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
JHHLHNBC_02710 | 3.7e-58 | gntR | K | rpiR family | ||
JHHLHNBC_02711 | 3.3e-37 | 2.7.1.194, 2.7.1.197, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_02712 | 1.2e-158 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JHHLHNBC_02713 | 7.6e-143 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
JHHLHNBC_02714 | 0.0 | clpL | O | associated with various cellular activities | ||
JHHLHNBC_02715 | 1.8e-63 | nrp | 1.20.4.1 | P | ArsC family | |
JHHLHNBC_02716 | 0.0 | fbp | 3.1.3.11 | G | phosphatase activity | |
JHHLHNBC_02717 | 9.8e-144 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
JHHLHNBC_02718 | 4.8e-112 | ylcC | 3.4.22.70 | M | Sortase family | |
JHHLHNBC_02719 | 6.1e-204 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
JHHLHNBC_02720 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
JHHLHNBC_02721 | 1.7e-197 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
JHHLHNBC_02722 | 2.3e-243 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_02723 | 2.9e-64 | S | pyridoxamine 5-phosphate | |||
JHHLHNBC_02724 | 3.3e-58 | |||||
JHHLHNBC_02725 | 0.0 | M | Glycosyl hydrolase family 59 | |||
JHHLHNBC_02726 | 9.5e-190 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_02727 | 2e-126 | kdgR | K | FCD domain | ||
JHHLHNBC_02728 | 1.8e-229 | G | Major Facilitator | |||
JHHLHNBC_02729 | 7.8e-267 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
JHHLHNBC_02730 | 0.0 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
JHHLHNBC_02731 | 1.1e-216 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
JHHLHNBC_02732 | 2.1e-279 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
JHHLHNBC_02733 | 4.6e-177 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_02734 | 1.4e-116 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
JHHLHNBC_02735 | 0.0 | M | Glycosyl hydrolase family 59 | |||
JHHLHNBC_02736 | 1.6e-78 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
JHHLHNBC_02737 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
JHHLHNBC_02738 | 2.4e-29 | |||||
JHHLHNBC_02739 | 6.5e-129 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
JHHLHNBC_02740 | 5.8e-86 | S | Phage portal protein | |||
JHHLHNBC_02741 | 2.3e-105 | S | peptidase activity | |||
JHHLHNBC_02742 | 1.1e-201 | S | peptidase activity | |||
JHHLHNBC_02743 | 5e-24 | S | peptidase activity | |||
JHHLHNBC_02744 | 9.4e-27 | S | Phage gp6-like head-tail connector protein | |||
JHHLHNBC_02745 | 1.2e-39 | S | Phage head-tail joining protein | |||
JHHLHNBC_02746 | 2.9e-66 | S | exonuclease activity | |||
JHHLHNBC_02747 | 4.4e-30 | |||||
JHHLHNBC_02748 | 1.5e-66 | |||||
JHHLHNBC_02749 | 5.1e-75 | O | OsmC-like protein | |||
JHHLHNBC_02750 | 2.3e-281 | lsa | S | ABC transporter | ||
JHHLHNBC_02755 | 1.3e-66 | 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 | ||
JHHLHNBC_02757 | 7e-80 | 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 | ||
JHHLHNBC_02758 | 2.2e-62 | rplO | J | Binds to the 23S rRNA | ||
JHHLHNBC_02759 | 1.7e-24 | rpmD | J | Ribosomal protein L30 | ||
JHHLHNBC_02760 | 2e-83 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
JHHLHNBC_02761 | 4.6e-58 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
JHHLHNBC_02762 | 3.5e-94 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
JHHLHNBC_02763 | 7.9e-67 | 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 | ||
JHHLHNBC_02764 | 8.5e-96 | 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 | ||
JHHLHNBC_02765 | 1.8e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
JHHLHNBC_02766 | 2.5e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
JHHLHNBC_02767 | 1.4e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
JHHLHNBC_02768 | 1.1e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
JHHLHNBC_02769 | 2.3e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
JHHLHNBC_02770 | 9.6e-110 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
JHHLHNBC_02771 | 1.1e-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 | ||
JHHLHNBC_02772 | 2.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
JHHLHNBC_02773 | 8.9e-153 | 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 | ||
JHHLHNBC_02774 | 4.5e-46 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
JHHLHNBC_02775 | 5.9e-109 | rplD | J | Forms part of the polypeptide exit tunnel | ||
JHHLHNBC_02776 | 8.9e-113 | 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 | ||
JHHLHNBC_02777 | 1.2e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
JHHLHNBC_02778 | 1.1e-278 | 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) | |
JHHLHNBC_02779 | 1.8e-254 | iolT | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02780 | 2.7e-103 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
JHHLHNBC_02781 | 2.2e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
JHHLHNBC_02782 | 3.6e-210 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
JHHLHNBC_02783 | 2.3e-133 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
JHHLHNBC_02784 | 6.4e-41 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JHHLHNBC_02785 | 3.3e-129 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JHHLHNBC_02786 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
JHHLHNBC_02787 | 6.9e-278 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
JHHLHNBC_02788 | 6.9e-184 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
JHHLHNBC_02789 | 7.8e-100 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
JHHLHNBC_02790 | 1.3e-287 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
JHHLHNBC_02791 | 1.9e-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 | ||
JHHLHNBC_02792 | 9e-102 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_02793 | 6e-146 | frlD | 2.7.1.218 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_02794 | 3.5e-113 | G | Phosphodiester glycosidase | |||
JHHLHNBC_02795 | 2.1e-153 | G | Phosphodiester glycosidase | |||
JHHLHNBC_02796 | 2.7e-288 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase N-terminal region | |
JHHLHNBC_02797 | 3.1e-206 | S | Protein of unknown function (DUF917) | |||
JHHLHNBC_02798 | 8.4e-224 | F | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
JHHLHNBC_02799 | 7.6e-117 | |||||
JHHLHNBC_02800 | 0.0 | S | Protein of unknown function (DUF1524) | |||
JHHLHNBC_02801 | 0.0 | 3.4.21.53 | O | Putative ATP-dependent Lon protease | ||
JHHLHNBC_02802 | 0.0 | S | PglZ domain | |||
JHHLHNBC_02803 | 4.3e-26 | |||||
JHHLHNBC_02804 | 1.2e-111 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
JHHLHNBC_02805 | 4.8e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
JHHLHNBC_02806 | 4e-78 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
JHHLHNBC_02807 | 2e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
JHHLHNBC_02808 | 6.7e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
JHHLHNBC_02809 | 1.7e-82 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
JHHLHNBC_02810 | 1e-81 | guaD | 3.5.4.12, 3.5.4.3, 3.5.4.33 | FJ | MafB19-like deaminase | |
JHHLHNBC_02811 | 3.8e-173 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
JHHLHNBC_02812 | 3e-231 | wbbX | GT2,GT4 | M | Glycosyl transferases group 1 | |
JHHLHNBC_02813 | 4.1e-77 | yttA | 2.7.13.3 | S | Pfam Transposase IS66 | |
JHHLHNBC_02814 | 2.3e-116 | F | DNA/RNA non-specific endonuclease | |||
JHHLHNBC_02815 | 2.9e-47 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
JHHLHNBC_02817 | 4.3e-258 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
JHHLHNBC_02818 | 1.9e-126 | |||||
JHHLHNBC_02819 | 3.4e-157 | dkgB | S | reductase | ||
JHHLHNBC_02820 | 5.3e-86 | nrdI | F | Belongs to the NrdI family | ||
JHHLHNBC_02821 | 2.3e-170 | D | Alpha beta | |||
JHHLHNBC_02822 | 4.4e-77 | K | Transcriptional regulator | |||
JHHLHNBC_02823 | 1.3e-122 | gph | 3.1.3.18 | S | haloacid dehalogenase-like hydrolase | |
JHHLHNBC_02824 | 2.7e-200 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
JHHLHNBC_02825 | 2e-94 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
JHHLHNBC_02826 | 2.5e-53 | |||||
JHHLHNBC_02827 | 2.3e-178 | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | ||
JHHLHNBC_02828 | 0.0 | yfgQ | P | E1-E2 ATPase | ||
JHHLHNBC_02829 | 1.9e-77 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
JHHLHNBC_02830 | 4.1e-51 | |||||
JHHLHNBC_02831 | 0.0 | pepF | E | Oligopeptidase F | ||
JHHLHNBC_02832 | 8.3e-285 | V | ABC transporter transmembrane region | |||
JHHLHNBC_02833 | 6e-177 | K | sequence-specific DNA binding | |||
JHHLHNBC_02834 | 1.1e-89 | |||||
JHHLHNBC_02835 | 1.1e-202 | L | PFAM transposase IS116 IS110 IS902 | |||
JHHLHNBC_02836 | 2.4e-26 | |||||
JHHLHNBC_02838 | 1.9e-72 | S | HNH endonuclease | |||
JHHLHNBC_02839 | 8.7e-78 | S | Phage terminase, small subunit | |||
JHHLHNBC_02840 | 0.0 | S | Phage Terminase | |||
JHHLHNBC_02842 | 6.1e-35 | |||||
JHHLHNBC_02843 | 6.7e-105 | S | Stage II sporulation protein M | |||
JHHLHNBC_02844 | 9.2e-167 | yeaC | S | ATPase family associated with various cellular activities (AAA) | ||
JHHLHNBC_02845 | 3.7e-182 | yeaD | S | Protein of unknown function DUF58 | ||
JHHLHNBC_02846 | 0.0 | yebA | E | Transglutaminase/protease-like homologues | ||
JHHLHNBC_02847 | 2.9e-212 | lsgC | M | Glycosyl transferases group 1 | ||
JHHLHNBC_02848 | 1.8e-251 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
JHHLHNBC_02849 | 1.3e-94 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
JHHLHNBC_02850 | 6.6e-40 | yjdF | S | Protein of unknown function (DUF2992) | ||
JHHLHNBC_02851 | 2.9e-210 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
JHHLHNBC_02852 | 1e-211 | maeN | C | 2-hydroxycarboxylate transporter family | ||
JHHLHNBC_02853 | 5.8e-259 | dcuS | 2.7.13.3 | T | Single cache domain 3 | |
JHHLHNBC_02854 | 6e-115 | dpiA | KT | cheY-homologous receiver domain | ||
JHHLHNBC_02855 | 1.4e-85 | |||||
JHHLHNBC_02857 | 1.4e-170 | V | ABC transporter | |||
JHHLHNBC_02858 | 8.3e-105 | sagI | S | ABC-2 type transporter | ||
JHHLHNBC_02859 | 1.5e-119 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_02860 | 1.3e-96 | |||||
JHHLHNBC_02861 | 5.2e-208 | T | signal transduction protein with a C-terminal ATPase domain | |||
JHHLHNBC_02862 | 3.3e-124 | rr02 | KT | LytTr DNA-binding domain | ||
JHHLHNBC_02863 | 5.5e-150 | 1.1.1.31 | I | NAD binding domain of 6-phosphogluconate dehydrogenase | ||
JHHLHNBC_02864 | 4.2e-68 | |||||
JHHLHNBC_02865 | 3.2e-167 | O | protein-N(PI)-phosphohistidine-lactose phosphotransferase system transporter activity | |||
JHHLHNBC_02868 | 1.4e-217 | sip | L | Belongs to the 'phage' integrase family | ||
JHHLHNBC_02869 | 1.5e-10 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_02871 | 2.1e-57 | |||||
JHHLHNBC_02872 | 4.5e-23 | |||||
JHHLHNBC_02873 | 3.3e-180 | yfeX | P | Peroxidase | ||
JHHLHNBC_02874 | 3.1e-116 | yhiD | S | MgtC family | ||
JHHLHNBC_02875 | 2.5e-308 | ybiT | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_02876 | 0.0 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
JHHLHNBC_02877 | 6.9e-112 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
JHHLHNBC_02878 | 5.9e-290 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JHHLHNBC_02879 | 6.4e-44 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | component | |
JHHLHNBC_02880 | 0.0 | celR | 2.7.1.202 | G | Mga helix-turn-helix domain | |
JHHLHNBC_02881 | 6.1e-58 | celC | 2.7.1.196, 2.7.1.205 | G | Phosphotransferase system cellobiose-specific component IIA | |
JHHLHNBC_02882 | 1.9e-25 | |||||
JHHLHNBC_02883 | 2.6e-242 | celD | 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 | ||
JHHLHNBC_02884 | 4e-130 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
JHHLHNBC_02885 | 0.0 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
JHHLHNBC_02886 | 3.1e-297 | 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 | |
JHHLHNBC_02887 | 4.5e-137 | epsG | 2.4.1.293 | GT2 | M | Glycosyltransferase like family 2 |
JHHLHNBC_02888 | 7.4e-222 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
JHHLHNBC_02889 | 2.3e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
JHHLHNBC_02890 | 3.8e-284 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
JHHLHNBC_02891 | 1.5e-162 | K | Transcriptional regulator | |||
JHHLHNBC_02892 | 1.1e-202 | L | PFAM transposase IS116 IS110 IS902 | |||
JHHLHNBC_02893 | 4.5e-76 | ohr | O | OsmC-like protein | ||
JHHLHNBC_02894 | 6e-108 | ypsA | S | Belongs to the UPF0398 family | ||
JHHLHNBC_02895 | 3.3e-120 | 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 | ||
JHHLHNBC_02896 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
JHHLHNBC_02897 | 1e-86 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
JHHLHNBC_02898 | 6.4e-106 | 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 | |
JHHLHNBC_02899 | 1.8e-113 | dnaD | L | DnaD domain protein | ||
JHHLHNBC_02900 | 1.6e-257 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
JHHLHNBC_02901 | 2.4e-220 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
JHHLHNBC_02902 | 7.2e-86 | ypmB | S | Protein conserved in bacteria | ||
JHHLHNBC_02903 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
JHHLHNBC_02904 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
JHHLHNBC_02905 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
JHHLHNBC_02906 | 1e-165 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
JHHLHNBC_02907 | 7.1e-173 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
JHHLHNBC_02908 | 7.8e-191 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
JHHLHNBC_02909 | 1.8e-256 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
JHHLHNBC_02910 | 8.2e-172 | |||||
JHHLHNBC_02911 | 2.6e-140 | |||||
JHHLHNBC_02912 | 3.7e-60 | yitW | S | Iron-sulfur cluster assembly protein | ||
JHHLHNBC_02913 | 5.5e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
JHHLHNBC_02914 | 2.1e-148 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
JHHLHNBC_02915 | 2.4e-127 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
JHHLHNBC_02916 | 4.1e-186 | 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 | ||
JHHLHNBC_02917 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
JHHLHNBC_02918 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
JHHLHNBC_02919 | 1.3e-173 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
JHHLHNBC_02921 | 2.9e-16 | |||||
JHHLHNBC_02922 | 2.2e-14 | ytgB | S | Transglycosylase associated protein | ||
JHHLHNBC_02923 | 2.9e-39 | 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 | ||
JHHLHNBC_02925 | 2e-169 | 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) | |
JHHLHNBC_02926 | 4.5e-182 | D | Alpha beta | |||
JHHLHNBC_02927 | 4.5e-185 | lipA | I | Carboxylesterase family | ||
JHHLHNBC_02928 | 1.3e-202 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
JHHLHNBC_02929 | 2.2e-78 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
JHHLHNBC_02930 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_02931 | 6.3e-19 | S | COG NOG38524 non supervised orthologous group | |||
JHHLHNBC_02932 | 6.8e-20 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
JHHLHNBC_02933 | 0.0 | pbpC | M | NTF2-like N-terminal transpeptidase domain | ||
JHHLHNBC_02934 | 3.9e-157 | 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 | |
JHHLHNBC_02935 | 3.2e-162 | rbsB | G | Periplasmic binding protein domain | ||
JHHLHNBC_02936 | 2.6e-164 | rbsC | U | Belongs to the binding-protein-dependent transport system permease family | ||
JHHLHNBC_02937 | 2e-280 | rbsA | 3.6.3.17 | G | ABC transporter | |
JHHLHNBC_02938 | 2.8e-64 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
JHHLHNBC_02939 | 9.3e-181 | rbsR | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
JHHLHNBC_02940 | 7e-150 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
JHHLHNBC_02941 | 1.6e-101 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
JHHLHNBC_02942 | 5.4e-150 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
JHHLHNBC_02943 | 2.6e-83 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
JHHLHNBC_02944 | 2.8e-128 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
JHHLHNBC_02945 | 3e-100 | P | cobalt transport | |||
JHHLHNBC_02946 | 2.1e-241 | P | ABC transporter | |||
JHHLHNBC_02947 | 2.2e-94 | S | ABC-type cobalt transport system, permease component | |||
JHHLHNBC_02949 | 2.5e-183 | scrR | K | Transcriptional regulator, LacI family | ||
JHHLHNBC_02953 | 4.4e-259 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
JHHLHNBC_02954 | 6.5e-266 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
JHHLHNBC_02955 | 2.1e-176 | M | Glycosyl transferase family 8 | |||
JHHLHNBC_02956 | 9.2e-172 | M | Glycosyl transferase family 8 | |||
JHHLHNBC_02957 | 6.7e-178 | M | Glycosyl transferase family 8 | |||
JHHLHNBC_02959 | 0.0 | secA2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
JHHLHNBC_02960 | 3.2e-220 | secY2 | U | SecY translocase | ||
JHHLHNBC_02961 | 1.9e-308 | asp1 | S | Accessory Sec system protein Asp1 | ||
JHHLHNBC_02962 | 0.0 | asp2 | 3.4.11.5 | S | Accessory Sec system GspB-transporter | |
JHHLHNBC_02963 | 2.6e-26 | asp3 | S | Accessory Sec secretory system ASP3 | ||
JHHLHNBC_02964 | 5.6e-280 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
JHHLHNBC_02965 | 6.7e-164 | |||||
JHHLHNBC_02966 | 5.8e-52 | |||||
JHHLHNBC_02967 | 2.2e-241 | citM | C | Citrate transporter | ||
JHHLHNBC_02968 | 1.3e-41 | |||||
JHHLHNBC_02969 | 1.8e-101 | kptA | J | Removes the 2'-phosphate from RNA via an intermediate in which the phosphate is ADP-ribosylated by NAD followed by a presumed transesterification to release the RNA and generate ADP- ribose 1''-2''-cyclic phosphate (APPR P). May function as an ADP- ribosylase | ||
JHHLHNBC_02970 | 9.3e-89 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_02971 | 9e-110 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
JHHLHNBC_02972 | 9.9e-58 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_02973 | 1.4e-90 | ORF00048 | ||||
JHHLHNBC_02974 | 3.3e-138 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
JHHLHNBC_02975 | 4.4e-169 | yjjC | V | ABC transporter | ||
JHHLHNBC_02976 | 3.1e-287 | M | Exporter of polyketide antibiotics | |||
JHHLHNBC_02977 | 7.3e-115 | K | Transcriptional regulator | |||
JHHLHNBC_02978 | 2.4e-259 | ypiB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_02979 | 6.7e-128 | S | membrane transporter protein | |||
JHHLHNBC_02980 | 5.2e-187 | K | Helix-turn-helix domain | |||
JHHLHNBC_02981 | 1.8e-164 | S | Alpha beta hydrolase | |||
JHHLHNBC_02982 | 3.6e-61 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
JHHLHNBC_02983 | 8.5e-128 | skfE | V | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_02984 | 6.9e-21 | |||||
JHHLHNBC_02985 | 3.1e-164 | oppF | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
JHHLHNBC_02986 | 8.2e-90 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
JHHLHNBC_02987 | 2.4e-56 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
JHHLHNBC_02988 | 2.1e-219 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
JHHLHNBC_02989 | 1.9e-127 | IQ | reductase | |||
JHHLHNBC_02990 | 5.9e-166 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
JHHLHNBC_02991 | 5.4e-173 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
JHHLHNBC_02992 | 2.6e-33 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
JHHLHNBC_02993 | 1.2e-169 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
JHHLHNBC_02994 | 2.8e-63 | yugI | 5.3.1.9 | J | general stress protein | |
JHHLHNBC_02995 | 1.1e-109 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
JHHLHNBC_02996 | 3e-184 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
JHHLHNBC_02997 | 5.1e-87 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
JHHLHNBC_02998 | 2.3e-116 | dedA | S | SNARE-like domain protein | ||
JHHLHNBC_02999 | 3.6e-114 | S | Protein of unknown function (DUF1461) | |||
JHHLHNBC_03000 | 7.7e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
JHHLHNBC_03001 | 3.7e-111 | yutD | S | Protein of unknown function (DUF1027) | ||
JHHLHNBC_03002 | 4e-267 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
JHHLHNBC_03003 | 3.1e-115 | S | Calcineurin-like phosphoesterase | |||
JHHLHNBC_03004 | 1.8e-117 | yibF | S | overlaps another CDS with the same product name | ||
JHHLHNBC_03005 | 5.2e-190 | yibE | S | overlaps another CDS with the same product name | ||
JHHLHNBC_03006 | 1e-53 | |||||
JHHLHNBC_03007 | 1.4e-256 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
JHHLHNBC_03008 | 1.3e-270 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
JHHLHNBC_03009 | 1.1e-133 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
JHHLHNBC_03010 | 9.5e-129 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
JHHLHNBC_03011 | 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 | ||
JHHLHNBC_03012 | 4.6e-58 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
JHHLHNBC_03013 | 5.3e-124 | terC | P | Integral membrane protein TerC family | ||
JHHLHNBC_03014 | 1.2e-158 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
JHHLHNBC_03015 | 1e-176 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
JHHLHNBC_03016 | 2.7e-224 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
JHHLHNBC_03017 | 1.6e-191 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
JHHLHNBC_03018 | 1.3e-97 | 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 | ||
JHHLHNBC_03019 | 8e-287 | dnaK | O | Heat shock 70 kDa protein | ||
JHHLHNBC_03020 | 6.7e-191 | 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 | ||
JHHLHNBC_03021 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
JHHLHNBC_03022 | 2.1e-35 | |||||
JHHLHNBC_03023 | 4.7e-82 | 6.3.3.2 | P | Protein conserved in bacteria | ||
JHHLHNBC_03024 | 7.1e-62 | |||||
JHHLHNBC_03025 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
JHHLHNBC_03026 | 2.6e-94 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
JHHLHNBC_03027 | 1.3e-90 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
JHHLHNBC_03028 | 9.4e-55 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
JHHLHNBC_03029 | 2.3e-150 | hutG | 3.5.3.8 | E | N-formylglutamate amidohydrolase | |
JHHLHNBC_03030 | 1.6e-35 | M | Host cell surface-exposed lipoprotein | |||
JHHLHNBC_03033 | 1.1e-202 | L | PFAM transposase IS116 IS110 IS902 | |||
JHHLHNBC_03034 | 4.6e-120 | S | B3/4 domain | |||
JHHLHNBC_03035 | 1.4e-26 | |||||
JHHLHNBC_03036 | 1.4e-246 | GT4 | M | transferase activity, transferring glycosyl groups | ||
JHHLHNBC_03037 | 7.6e-183 | |||||
JHHLHNBC_03038 | 0.0 | kefA | D | nuclear chromosome segregation | ||
JHHLHNBC_03040 | 4e-223 | 3.4.24.40 | S | Cysteine-rich secretory protein family | ||
JHHLHNBC_03042 | 2.8e-183 | |||||
JHHLHNBC_03043 | 2.1e-113 | |||||
JHHLHNBC_03044 | 2.6e-299 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
JHHLHNBC_03045 | 2.2e-279 | tagE2 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
JHHLHNBC_03046 | 3.9e-187 | mocA | S | Oxidoreductase | ||
JHHLHNBC_03047 | 3.3e-201 | S | CAAX protease self-immunity | |||
JHHLHNBC_03048 | 8.2e-87 | dps | P | Belongs to the Dps family | ||
JHHLHNBC_03049 | 2.6e-230 | ywhK | S | Membrane | ||
JHHLHNBC_03050 | 4.3e-135 | |||||
JHHLHNBC_03051 | 5.6e-152 | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_03052 | 0.0 | V | FtsX-like permease family | |||
JHHLHNBC_03053 | 1.5e-135 | cysA | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_03054 | 3.1e-56 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_03057 | 8.8e-107 | K | Transcriptional regulator, AbiEi antitoxin | |||
JHHLHNBC_03058 | 5.1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
JHHLHNBC_03059 | 8.9e-245 | 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) | |
JHHLHNBC_03060 | 1e-303 | frvR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_03061 | 3.1e-297 | frvR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_03062 | 7.2e-259 | lysP | E | amino acid | ||
JHHLHNBC_03063 | 1.6e-131 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
JHHLHNBC_03064 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_03065 | 4.1e-98 | |||||
JHHLHNBC_03066 | 3.7e-96 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_03067 | 2.6e-167 | S | Bacterial protein of unknown function (DUF916) | |||
JHHLHNBC_03068 | 5.1e-99 | |||||
JHHLHNBC_03069 | 7.4e-152 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
JHHLHNBC_03070 | 1.1e-267 | S | Virulence-associated protein E | |||
JHHLHNBC_03072 | 9.1e-23 | L | Helix-turn-helix domain | |||
JHHLHNBC_03073 | 1.8e-60 | rplQ | J | Ribosomal protein L17 | ||
JHHLHNBC_03074 | 6.2e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
JHHLHNBC_03075 | 4e-63 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
JHHLHNBC_03076 | 3.6e-58 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
JHHLHNBC_03077 | 6.6e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
JHHLHNBC_03078 | 7e-33 | 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 | ||
JHHLHNBC_03079 | 2.3e-119 | 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 | |
JHHLHNBC_03080 | 1.4e-218 | 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 | ||
JHHLHNBC_03081 | 5.9e-43 | S | Phage gp6-like head-tail connector protein | |||
JHHLHNBC_03082 | 2.3e-271 | S | Phage capsid family | |||
JHHLHNBC_03083 | 1.5e-214 | S | Phage portal protein | |||
JHHLHNBC_03084 | 1.9e-20 | |||||
JHHLHNBC_03085 | 0.0 | terL | S | overlaps another CDS with the same product name | ||
JHHLHNBC_03086 | 2.2e-76 | terS | L | Phage terminase, small subunit | ||
JHHLHNBC_03087 | 3.9e-24 | L | Phage-associated protein | |||
JHHLHNBC_03089 | 3.5e-35 | S | peptidoglycan catabolic process | |||
JHHLHNBC_03090 | 2.5e-49 | S | peptidoglycan catabolic process | |||
JHHLHNBC_03091 | 3.6e-196 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
JHHLHNBC_03092 | 2.9e-232 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
JHHLHNBC_03093 | 3.1e-107 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
JHHLHNBC_03094 | 1e-47 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
JHHLHNBC_03095 | 2.3e-20 | |||||
JHHLHNBC_03096 | 6.5e-260 | glnPH2 | P | ABC transporter permease | ||
JHHLHNBC_03097 | 2.4e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_03098 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
JHHLHNBC_03099 | 1.3e-171 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
JHHLHNBC_03100 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
JHHLHNBC_03101 | 9.5e-286 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
JHHLHNBC_03102 | 3e-173 | S | Aldo keto reductase | |||
JHHLHNBC_03103 | 9.3e-155 | bioC | 2.1.1.187, 2.1.1.197 | Q | Protein-L-isoaspartate(D-aspartate) O-methyltransferase (PCMT) | |
JHHLHNBC_03104 | 4.8e-90 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
JHHLHNBC_03105 | 3.5e-239 | dinF | V | MatE | ||
JHHLHNBC_03106 | 0.0 | ykcB | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | ||
JHHLHNBC_03107 | 3.2e-71 | S | GtrA-like protein | |||
JHHLHNBC_03108 | 1.3e-128 | K | cheY-homologous receiver domain | |||
JHHLHNBC_03109 | 3.9e-240 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
JHHLHNBC_03110 | 1.2e-67 | yqkB | S | Belongs to the HesB IscA family | ||
JHHLHNBC_03111 | 4.9e-122 | drgA | C | Nitroreductase family | ||
JHHLHNBC_03112 | 1e-204 | lctO | C | IMP dehydrogenase / GMP reductase domain | ||
JHHLHNBC_03113 | 9.3e-147 | dprA | LU | DNA protecting protein DprA | ||
JHHLHNBC_03114 | 1.5e-138 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
JHHLHNBC_03115 | 2.5e-150 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
JHHLHNBC_03117 | 1.3e-87 | S | Domain of unknown function (DUF4918) | |||
JHHLHNBC_03118 | 1e-54 | |||||
JHHLHNBC_03119 | 1.4e-13 | |||||
JHHLHNBC_03120 | 9.5e-79 | S | Psort location Cytoplasmic, score | |||
JHHLHNBC_03121 | 1.1e-249 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
JHHLHNBC_03122 | 1e-40 | yozE | S | Belongs to the UPF0346 family | ||
JHHLHNBC_03123 | 7.1e-92 | msrA | 1.8.4.11, 1.8.4.12 | C | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
JHHLHNBC_03124 | 2.4e-113 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
JHHLHNBC_03125 | 2.8e-146 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
JHHLHNBC_03127 | 1.7e-154 | DegV | S | EDD domain protein, DegV family | ||
JHHLHNBC_03128 | 9.3e-110 | hly | S | protein, hemolysin III | ||
JHHLHNBC_03129 | 3.6e-93 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
JHHLHNBC_03130 | 1.3e-189 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
JHHLHNBC_03131 | 2.1e-306 | yfmR | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_03132 | 1.6e-84 | |||||
JHHLHNBC_03133 | 4.7e-224 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
JHHLHNBC_03134 | 8.7e-143 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
JHHLHNBC_03135 | 2.6e-196 | S | Tetratricopeptide repeat protein | |||
JHHLHNBC_03136 | 4.2e-77 | usp5 | T | universal stress protein | ||
JHHLHNBC_03137 | 4.7e-64 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_03138 | 1.1e-144 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
JHHLHNBC_03139 | 1.5e-91 | yhbO | 3.5.1.124 | S | DJ-1/PfpI family | |
JHHLHNBC_03140 | 3.3e-283 | cydA | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit I | |
JHHLHNBC_03141 | 5.7e-186 | cydB | 1.10.3.14 | C | Cytochrome bd terminal oxidase subunit II | |
JHHLHNBC_03142 | 5.6e-26 | |||||
JHHLHNBC_03146 | 1.1e-36 | tnp2PF3 | L | Transposase | ||
JHHLHNBC_03147 | 8.7e-34 | L | Putative transposase of IS4/5 family (DUF4096) | |||
JHHLHNBC_03148 | 9.9e-228 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
JHHLHNBC_03149 | 4e-248 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
JHHLHNBC_03150 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
JHHLHNBC_03151 | 4.8e-72 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
JHHLHNBC_03152 | 2.7e-173 | msmX | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_03153 | 6.6e-229 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
JHHLHNBC_03154 | 8.4e-168 | malE | G | Bacterial extracellular solute-binding protein | ||
JHHLHNBC_03155 | 5.6e-205 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_03156 | 2.5e-134 | malG | P | ABC transporter permease | ||
JHHLHNBC_03157 | 6.6e-136 | yvdE | K | helix_turn _helix lactose operon repressor | ||
JHHLHNBC_03158 | 7.6e-67 | tnp2PF3 | L | Transposase | ||
JHHLHNBC_03159 | 2.5e-58 | L | Putative transposase of IS4/5 family (DUF4096) | |||
JHHLHNBC_03160 | 7e-14 | S | Class II bacteriocin | |||
JHHLHNBC_03161 | 4.7e-24 | spiA | S | Enterocin A Immunity | ||
JHHLHNBC_03164 | 1.1e-28 | |||||
JHHLHNBC_03165 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
JHHLHNBC_03166 | 2.4e-163 | mesE | M | Transport protein ComB | ||
JHHLHNBC_03167 | 5.1e-185 | P | Ammonium Transporter Family | |||
JHHLHNBC_03168 | 4.1e-214 | P | Pyridine nucleotide-disulphide oxidoreductase | |||
JHHLHNBC_03169 | 2.5e-217 | L | Belongs to the 'phage' integrase family | |||
JHHLHNBC_03170 | 7.3e-127 | IQ | reductase | |||
JHHLHNBC_03171 | 1e-165 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
JHHLHNBC_03172 | 2.4e-173 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
JHHLHNBC_03173 | 4.5e-33 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
JHHLHNBC_03174 | 2.6e-172 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
JHHLHNBC_03175 | 1.7e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
JHHLHNBC_03176 | 5.7e-239 | tilS | 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 | |
JHHLHNBC_03177 | 1.1e-83 | yabR | J | RNA binding | ||
JHHLHNBC_03178 | 6.7e-66 | divIC | D | Septum formation initiator | ||
JHHLHNBC_03179 | 1.9e-37 | yabO | J | S4 domain protein | ||
JHHLHNBC_03180 | 5.5e-281 | yabM | S | Polysaccharide biosynthesis protein | ||
JHHLHNBC_03181 | 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 | ||
JHHLHNBC_03182 | 3.1e-101 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
JHHLHNBC_03183 | 5.1e-113 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
JHHLHNBC_03184 | 8.2e-190 | I | carboxylic ester hydrolase activity | |||
JHHLHNBC_03185 | 1.2e-255 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
JHHLHNBC_03186 | 4.4e-143 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
JHHLHNBC_03187 | 8.6e-99 | K | Helix-turn-helix domain | |||
JHHLHNBC_03189 | 1.4e-113 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
JHHLHNBC_03190 | 3.1e-92 | yjgM | K | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_03191 | 2.4e-133 | farR | K | Helix-turn-helix domain | ||
JHHLHNBC_03192 | 6.9e-161 | gatY | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_03193 | 9.9e-80 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_03194 | 1.6e-48 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_03195 | 4.7e-252 | gatC | G | PTS system sugar-specific permease component | ||
JHHLHNBC_03196 | 2.2e-279 | rhaB | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
JHHLHNBC_03197 | 3.7e-162 | G | Fructose-bisphosphate aldolase class-II | |||
JHHLHNBC_03198 | 5.3e-246 | licR | 2.7.1.194, 2.7.1.200, 2.7.1.202, 2.7.1.204 | K | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
JHHLHNBC_03199 | 1.9e-68 | ahaA | 2.7.1.191 | G | PTS system fructose IIA component | |
JHHLHNBC_03200 | 1.1e-217 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
JHHLHNBC_03201 | 1.7e-72 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
JHHLHNBC_03202 | 5.3e-256 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
JHHLHNBC_03203 | 2.4e-256 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
JHHLHNBC_03204 | 1.6e-185 | 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 | |
JHHLHNBC_03205 | 1.3e-196 | 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 | |
JHHLHNBC_03206 | 2.1e-61 | |||||
JHHLHNBC_03207 | 3.9e-48 | K | sequence-specific DNA binding | |||
JHHLHNBC_03208 | 9.1e-74 | 3.6.1.55 | L | NUDIX domain | ||
JHHLHNBC_03209 | 1.9e-150 | EG | EamA-like transporter family | |||
JHHLHNBC_03211 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
JHHLHNBC_03212 | 5.1e-70 | rplI | J | Binds to the 23S rRNA | ||
JHHLHNBC_03213 | 3.2e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
JHHLHNBC_03214 | 2.1e-221 | |||||
JHHLHNBC_03215 | 0.0 | sacX | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_03216 | 1.1e-162 | 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 | |
JHHLHNBC_03217 | 3.5e-199 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
JHHLHNBC_03218 | 3.6e-157 | K | Helix-turn-helix domain, rpiR family | |||
JHHLHNBC_03219 | 1.8e-107 | K | Transcriptional regulator C-terminal region | |||
JHHLHNBC_03220 | 4.9e-128 | V | ABC transporter, ATP-binding protein | |||
JHHLHNBC_03221 | 0.0 | ylbB | V | ABC transporter permease | ||
JHHLHNBC_03222 | 1.2e-207 | 4.1.1.52 | S | Amidohydrolase | ||
JHHLHNBC_03223 | 4.9e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
JHHLHNBC_03224 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
JHHLHNBC_03225 | 1.2e-55 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
JHHLHNBC_03227 | 2.4e-207 | yxaM | EGP | Major facilitator Superfamily | ||
JHHLHNBC_03228 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
JHHLHNBC_03229 | 5.5e-132 | |||||
JHHLHNBC_03230 | 2.6e-111 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
JHHLHNBC_03231 | 2.1e-62 | ybbR | S | YbbR-like protein | ||
JHHLHNBC_03232 | 2.6e-255 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
JHHLHNBC_03233 | 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 | |
JHHLHNBC_03234 | 0.0 | pepF2 | E | Oligopeptidase F | ||
JHHLHNBC_03235 | 9.7e-91 | S | VanZ like family | |||
JHHLHNBC_03236 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
JHHLHNBC_03237 | 1.2e-09 | |||||
JHHLHNBC_03238 | 7.4e-236 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
JHHLHNBC_03239 | 9.6e-95 | M1-874 | K | Domain of unknown function (DUF1836) | ||
JHHLHNBC_03240 | 1.4e-300 | cpdB | 3.1.3.6, 3.1.4.16 | F | 5'-nucleotidase, C-terminal domain | |
JHHLHNBC_03241 | 2.4e-145 | |||||
JHHLHNBC_03242 | 1.3e-19 | S | Protein of unknown function (DUF2929) | |||
JHHLHNBC_03243 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
JHHLHNBC_03244 | 1.5e-127 | rarA | L | recombination factor protein RarA | ||
JHHLHNBC_03249 | 8.5e-17 | yvaF | K | Bacterial regulatory proteins, tetR family | ||
JHHLHNBC_03250 | 1.7e-150 | I | Alpha beta | |||
JHHLHNBC_03251 | 1.4e-61 | aes | I | esterase lipase | ||
JHHLHNBC_03252 | 9.8e-70 | aes | I | esterase lipase | ||
JHHLHNBC_03253 | 2.3e-113 | K | Psort location Cytoplasmic, score | |||
JHHLHNBC_03254 | 0.0 | M | Glycosyl hydrolase family 59 | |||
JHHLHNBC_03255 | 6.5e-298 | ybeC | E | amino acid | ||
JHHLHNBC_03256 | 1.3e-93 | sigH | K | Sigma-70 region 2 | ||
JHHLHNBC_03258 | 1.4e-198 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
JHHLHNBC_03259 | 7e-164 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
JHHLHNBC_03260 | 3.4e-29 | |||||
JHHLHNBC_03262 | 2.1e-191 | M | Glycosyltransferase like family 2 | |||
JHHLHNBC_03263 | 7.4e-160 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
JHHLHNBC_03264 | 2.1e-79 | fld | C | Flavodoxin | ||
JHHLHNBC_03265 | 3.9e-179 | yihY | S | Belongs to the UPF0761 family | ||
JHHLHNBC_03266 | 1.8e-259 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
JHHLHNBC_03267 | 2.7e-111 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_03268 | 8.3e-240 | pepS | E | Thermophilic metalloprotease (M29) | ||
JHHLHNBC_03269 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
JHHLHNBC_03270 | 1.2e-09 | |||||
JHHLHNBC_03272 | 1.9e-71 | S | Domain of unknown function (DUF3284) | |||
JHHLHNBC_03273 | 1.2e-47 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_03274 | 1.2e-241 | yfmL | L | DEAD DEAH box helicase | ||
JHHLHNBC_03275 | 2.9e-176 | mocA | S | Oxidoreductase | ||
JHHLHNBC_03276 | 2e-61 | S | Domain of unknown function (DUF4828) | |||
JHHLHNBC_03277 | 4.2e-59 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_03278 | 8.9e-125 | lys | M | Glycosyl hydrolases family 25 | ||
JHHLHNBC_03279 | 2.7e-28 | |||||
JHHLHNBC_03280 | 9.3e-119 | qmcA | O | prohibitin homologues | ||
JHHLHNBC_03281 | 5.6e-166 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
JHHLHNBC_03282 | 1e-81 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_03283 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
JHHLHNBC_03284 | 6.2e-165 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
JHHLHNBC_03285 | 8.5e-146 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_03286 | 9e-215 | yttB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_03287 | 0.0 | nagZ | 3.2.1.52 | G | Glycosyl hydrolase family 3 N terminal domain | |
JHHLHNBC_03288 | 8.5e-254 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
JHHLHNBC_03289 | 5e-190 | yegS | 2.7.1.107 | G | Lipid kinase | |
JHHLHNBC_03290 | 3e-278 | 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) | |
JHHLHNBC_03291 | 6.2e-199 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
JHHLHNBC_03292 | 4.5e-29 | |||||
JHHLHNBC_03293 | 2e-200 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JHHLHNBC_03294 | 0.0 | pepF | E | oligoendopeptidase F | ||
JHHLHNBC_03295 | 5.8e-163 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
JHHLHNBC_03296 | 3.8e-167 | T | Calcineurin-like phosphoesterase superfamily domain | |||
JHHLHNBC_03297 | 3e-134 | znuB | U | ABC 3 transport family | ||
JHHLHNBC_03298 | 4.1e-130 | fhuC | 3.6.3.35 | P | ABC transporter | |
JHHLHNBC_03299 | 2e-58 | |||||
JHHLHNBC_03300 | 1.2e-196 | S | Protein conserved in bacteria | |||
JHHLHNBC_03301 | 1.8e-262 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
JHHLHNBC_03302 | 4.5e-191 | rgpB | GT2 | M | Glycosyl transferase family 2 | |
JHHLHNBC_03303 | 2.4e-127 | welB | S | Glycosyltransferase like family 2 | ||
JHHLHNBC_03304 | 2.8e-151 | S | Glycosyl transferase family 2 | |||
JHHLHNBC_03305 | 1.1e-253 | S | O-antigen ligase like membrane protein | |||
JHHLHNBC_03306 | 3.5e-207 | gntP | EG | Gluconate | ||
JHHLHNBC_03307 | 7.6e-24 | gntK | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
JHHLHNBC_03309 | 3.1e-218 | 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 | ||
JHHLHNBC_03310 | 1e-122 | K | response regulator | |||
JHHLHNBC_03311 | 9.8e-208 | T | PhoQ Sensor | |||
JHHLHNBC_03312 | 2.7e-48 | 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 | |
JHHLHNBC_03313 | 5.2e-78 | yodP | 2.3.1.264 | K | FR47-like protein | |
JHHLHNBC_03314 | 5.2e-83 | ydcK | S | Belongs to the SprT family | ||
JHHLHNBC_03315 | 3.3e-130 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_03316 | 4.6e-139 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
JHHLHNBC_03317 | 6.4e-174 | ABC-SBP | S | ABC transporter | ||
JHHLHNBC_03318 | 1.6e-73 | |||||
JHHLHNBC_03319 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
JHHLHNBC_03320 | 4.6e-171 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
JHHLHNBC_03321 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_03322 | 1e-78 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
JHHLHNBC_03323 | 1.2e-216 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
JHHLHNBC_03324 | 5.9e-185 | lipA | I | Carboxylesterase family | ||
JHHLHNBC_03325 | 1.5e-180 | D | Alpha beta | |||
JHHLHNBC_03326 | 8.8e-170 | 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) | |
JHHLHNBC_03327 | 1.4e-270 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
JHHLHNBC_03328 | 8.6e-09 | S | Protein of unknown function (DUF4044) | |||
JHHLHNBC_03329 | 1.7e-105 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
JHHLHNBC_03330 | 1e-113 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
JHHLHNBC_03331 | 3e-184 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
JHHLHNBC_03332 | 9.2e-95 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Cobalamin adenosyltransferase | |
JHHLHNBC_03333 | 1.3e-88 | S | ECF transporter, substrate-specific component | |||
JHHLHNBC_03334 | 3.1e-63 | S | Domain of unknown function (DUF4430) | |||
JHHLHNBC_03335 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
JHHLHNBC_03336 | 5.9e-79 | F | nucleoside 2-deoxyribosyltransferase | |||
JHHLHNBC_03337 | 1.3e-159 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
JHHLHNBC_03338 | 1.5e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
JHHLHNBC_03339 | 1.2e-76 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
JHHLHNBC_03340 | 1.8e-30 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
JHHLHNBC_03341 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
JHHLHNBC_03342 | 3.4e-07 | |||||
JHHLHNBC_03344 | 4.8e-70 | S | Domain of unknown function (DUF3284) | |||
JHHLHNBC_03345 | 6.8e-48 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_03346 | 4.5e-236 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
JHHLHNBC_03347 | 7e-178 | mocA | S | Oxidoreductase | ||
JHHLHNBC_03348 | 2e-61 | S | Domain of unknown function (DUF4828) | |||
JHHLHNBC_03349 | 6.3e-215 | lsgC | M | Glycosyl transferases group 1 | ||
JHHLHNBC_03350 | 1.7e-128 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
JHHLHNBC_03351 | 3.5e-160 | ymfH | S | Peptidase M16 | ||
JHHLHNBC_03352 | 0.0 | pepF | E | Oligopeptidase F | ||
JHHLHNBC_03353 | 2.9e-285 | V | ABC transporter transmembrane region | |||
JHHLHNBC_03354 | 1.8e-176 | K | sequence-specific DNA binding | |||
JHHLHNBC_03355 | 6.9e-95 | |||||
JHHLHNBC_03356 | 8.3e-90 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
JHHLHNBC_03357 | 1.1e-170 | mleP | S | Sodium Bile acid symporter family | ||
JHHLHNBC_03358 | 0.0 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
JHHLHNBC_03359 | 9.9e-29 | |||||
JHHLHNBC_03360 | 2.8e-124 | S | zinc-ribbon domain | |||
JHHLHNBC_03361 | 2.9e-204 | pbpX1 | V | Beta-lactamase | ||
JHHLHNBC_03362 | 1.3e-164 | K | AI-2E family transporter | |||
JHHLHNBC_03363 | 4.1e-127 | srtA | 3.4.22.70 | M | Sortase family | |
JHHLHNBC_03364 | 2.6e-65 | gtcA | S | Teichoic acid glycosylation protein | ||
JHHLHNBC_03365 | 1.3e-168 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
JHHLHNBC_03367 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_03368 | 1.1e-169 | gbuC | E | glycine betaine | ||
JHHLHNBC_03369 | 1.1e-137 | proW | E | glycine betaine | ||
JHHLHNBC_03370 | 5.9e-222 | gbuA | 3.6.3.32 | E | glycine betaine | |
JHHLHNBC_03371 | 8.1e-134 | sfsA | S | Belongs to the SfsA family | ||
JHHLHNBC_03372 | 2.2e-68 | usp1 | T | Universal stress protein family | ||
JHHLHNBC_03373 | 2.1e-251 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
JHHLHNBC_03374 | 1e-44 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
JHHLHNBC_03376 | 9.3e-192 | fic | S | Fic/DOC family | ||
JHHLHNBC_03377 | 9.3e-164 | thrB | 2.7.1.39, 4.2.3.1 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
JHHLHNBC_03378 | 5.1e-276 | thrC | 4.2.3.1 | E | Threonine synthase | |
JHHLHNBC_03379 | 2.3e-226 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
JHHLHNBC_03380 | 2.7e-252 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
JHHLHNBC_03381 | 2.4e-151 | yqiK | S | SPFH domain / Band 7 family | ||
JHHLHNBC_03382 | 3.4e-62 | |||||
JHHLHNBC_03383 | 4.5e-162 | pfoS | S | Phosphotransferase system, EIIC | ||
JHHLHNBC_03384 | 1.6e-161 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
JHHLHNBC_03385 | 7.4e-214 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
JHHLHNBC_03386 | 3.5e-221 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
JHHLHNBC_03387 | 1.6e-87 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
JHHLHNBC_03388 | 3.5e-103 | yjbF | S | SNARE associated Golgi protein | ||
JHHLHNBC_03389 | 3.9e-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 | |
JHHLHNBC_03390 | 6.2e-196 | 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 | |
JHHLHNBC_03391 | 1.3e-207 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
JHHLHNBC_03392 | 1e-32 | |||||
JHHLHNBC_03393 | 0.0 | K | helix_turn_helix, arabinose operon control protein | |||
JHHLHNBC_03394 | 1.1e-132 | |||||
JHHLHNBC_03395 | 5.7e-22 | 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 | ||
JHHLHNBC_03396 | 2.2e-265 | frvR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_03397 | 5e-268 | lysP | E | amino acid | ||
JHHLHNBC_03399 | 1.7e-128 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
JHHLHNBC_03400 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_03401 | 1.6e-97 | |||||
JHHLHNBC_03402 | 3.3e-100 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_03403 | 2.7e-191 | S | Bacterial protein of unknown function (DUF916) | |||
JHHLHNBC_03404 | 9.9e-103 | |||||
JHHLHNBC_03405 | 2.6e-94 | comFC | S | Competence protein | ||
JHHLHNBC_03406 | 1.7e-232 | comFA | L | Helicase C-terminal domain protein | ||
JHHLHNBC_03407 | 1.2e-117 | yvyE | 3.4.13.9 | S | YigZ family | |
JHHLHNBC_03408 | 2e-186 | rny | S | Endoribonuclease that initiates mRNA decay | ||
JHHLHNBC_03409 | 6.3e-45 | 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) | |
JHHLHNBC_03410 | 9.2e-209 | camS | S | sex pheromone | ||
JHHLHNBC_03411 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
JHHLHNBC_03412 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
JHHLHNBC_03413 | 1.2e-130 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
JHHLHNBC_03414 | 1.4e-159 | S | response to antibiotic | |||
JHHLHNBC_03416 | 8.7e-248 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
JHHLHNBC_03417 | 8.4e-54 | |||||
JHHLHNBC_03418 | 1.6e-80 | |||||
JHHLHNBC_03419 | 2.3e-72 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
JHHLHNBC_03420 | 4.3e-32 | |||||
JHHLHNBC_03421 | 1.3e-93 | yhbS | S | acetyltransferase | ||
JHHLHNBC_03422 | 1.3e-282 | T | PhoQ Sensor | |||
JHHLHNBC_03423 | 4.9e-131 | K | response regulator | |||
JHHLHNBC_03424 | 1.8e-63 | S | SdpI/YhfL protein family | |||
JHHLHNBC_03425 | 4.5e-149 | 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 | |
JHHLHNBC_03426 | 2.3e-156 | |||||
JHHLHNBC_03428 | 1.8e-231 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
JHHLHNBC_03429 | 8.7e-251 | yclM | 2.7.2.4 | E | Belongs to the aspartokinase family | |
JHHLHNBC_03430 | 4.7e-168 | yqiK | S | SPFH domain / Band 7 family | ||
JHHLHNBC_03431 | 1.3e-67 | |||||
JHHLHNBC_03432 | 1.2e-154 | pfoS | S | Phosphotransferase system, EIIC | ||
JHHLHNBC_03433 | 7.8e-180 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
JHHLHNBC_03434 | 5e-176 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
JHHLHNBC_03435 | 1.3e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_03436 | 9.2e-82 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
JHHLHNBC_03437 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
JHHLHNBC_03438 | 1.4e-63 | S | Family of unknown function (DUF5322) | |||
JHHLHNBC_03439 | 1.9e-174 | XK27_06930 | V | domain protein | ||
JHHLHNBC_03440 | 3.3e-101 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_03441 | 3.8e-145 | S | Alpha/beta hydrolase family | |||
JHHLHNBC_03442 | 5.6e-127 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
JHHLHNBC_03443 | 7.3e-264 | 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 | ||
JHHLHNBC_03444 | 1.5e-68 | S | Domain of unknown function (DUF3284) | |||
JHHLHNBC_03445 | 9.7e-208 | S | Bacterial protein of unknown function (DUF871) | |||
JHHLHNBC_03446 | 1.7e-51 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_03447 | 5.3e-101 | |||||
JHHLHNBC_03448 | 9.2e-144 | lutA | C | Cysteine-rich domain | ||
JHHLHNBC_03449 | 2.8e-290 | lutB | C | 4Fe-4S dicluster domain | ||
JHHLHNBC_03450 | 9.5e-132 | yrjD | S | LUD domain | ||
JHHLHNBC_03451 | 2.9e-99 | 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 | ||
JHHLHNBC_03452 | 2.1e-231 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_03453 | 1.4e-300 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_03454 | 8e-163 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
JHHLHNBC_03455 | 1.2e-177 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
JHHLHNBC_03456 | 8.7e-198 | oppD | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_03457 | 3.4e-180 | oppF | P | Belongs to the ABC transporter superfamily | ||
JHHLHNBC_03458 | 5e-116 | gpm5 | 3.1.3.3, 5.4.2.11 | G | phosphoglycerate mutase | |
JHHLHNBC_03459 | 5e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
JHHLHNBC_03460 | 4.8e-37 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
JHHLHNBC_03461 | 1.3e-123 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
JHHLHNBC_03462 | 1.8e-165 | XK27_00670 | S | ABC transporter | ||
JHHLHNBC_03463 | 2.9e-155 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
JHHLHNBC_03464 | 5.2e-142 | cmpC | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_03465 | 1.4e-170 | yhfP | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
JHHLHNBC_03466 | 4e-165 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
JHHLHNBC_03467 | 5.8e-97 | iolD | 3.7.1.22 | E | Involved in the cleavage of the C1-C2 bond of 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (THcHDO) to yield 5-deoxy- glucuronate (5DG) | |
JHHLHNBC_03468 | 1.1e-192 | iolG | 1.1.1.18, 1.1.1.369 | C | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
JHHLHNBC_03469 | 4.1e-195 | iolG2 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
JHHLHNBC_03470 | 3.6e-176 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
JHHLHNBC_03471 | 3e-159 | iolJ | 4.1.2.13, 4.1.2.29 | G | Fructose-bisphosphate aldolase class-II | |
JHHLHNBC_03472 | 1.7e-66 | iolK | S | Tautomerase enzyme | ||
JHHLHNBC_03473 | 1.4e-161 | iolI | 5.3.99.11 | G | Xylose isomerase-like TIM barrel | |
JHHLHNBC_03474 | 6.4e-170 | iolH | G | Xylose isomerase-like TIM barrel | ||
JHHLHNBC_03475 | 1.5e-147 | gntR | K | rpiR family | ||
JHHLHNBC_03476 | 1.6e-169 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
JHHLHNBC_03477 | 2.6e-52 | ybjQ | S | Belongs to the UPF0145 family | ||
JHHLHNBC_03478 | 1.4e-92 | nudC | 1.3.7.1, 3.6.1.22 | L | NUDIX domain | |
JHHLHNBC_03479 | 4.5e-158 | 3.5.1.10 | C | nadph quinone reductase | ||
JHHLHNBC_03480 | 5.9e-244 | amt | P | ammonium transporter | ||
JHHLHNBC_03481 | 3.4e-177 | yfeX | P | Peroxidase | ||
JHHLHNBC_03482 | 2.9e-21 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
JHHLHNBC_03483 | 6.6e-53 | trxA | O | Belongs to the thioredoxin family | ||
JHHLHNBC_03484 | 4.2e-294 | 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 | |
JHHLHNBC_03485 | 3.4e-238 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
JHHLHNBC_03486 | 4e-37 | 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 | |
JHHLHNBC_03487 | 1.1e-67 | usp1 | T | Universal stress protein family | ||
JHHLHNBC_03488 | 1.6e-251 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
JHHLHNBC_03489 | 1.1e-46 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
JHHLHNBC_03490 | 9.8e-64 | S | Phage derived protein Gp49-like (DUF891) | |||
JHHLHNBC_03491 | 2.3e-38 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_03492 | 2.4e-104 | tag | 3.2.2.20 | L | glycosylase | |
JHHLHNBC_03493 | 1.1e-110 | K | Transcriptional | |||
JHHLHNBC_03494 | 1.1e-193 | yceJ | EGP | Major facilitator Superfamily | ||
JHHLHNBC_03495 | 1.6e-48 | K | Helix-turn-helix domain | |||
JHHLHNBC_03496 | 6.5e-257 | L | Exonuclease | |||
JHHLHNBC_03497 | 2.7e-15 | |||||
JHHLHNBC_03498 | 8.5e-53 | |||||
JHHLHNBC_03500 | 2e-83 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
JHHLHNBC_03501 | 2.5e-101 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
JHHLHNBC_03502 | 3.8e-179 | 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 | ||
JHHLHNBC_03503 | 2.1e-282 | mga | K | Mga helix-turn-helix domain | ||
JHHLHNBC_03504 | 5.5e-80 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
JHHLHNBC_03505 | 1.6e-171 | whiA | K | May be required for sporulation | ||
JHHLHNBC_03506 | 7.7e-191 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
JHHLHNBC_03507 | 1.3e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
JHHLHNBC_03508 | 8.7e-35 | |||||
JHHLHNBC_03509 | 2.5e-71 | S | magnesium ion binding | |||
JHHLHNBC_03510 | 4.4e-10 | S | C-5 cytosine-specific DNA methylase | |||
JHHLHNBC_03511 | 9.8e-107 | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | ||
JHHLHNBC_03512 | 4.3e-124 | S | DNA methylation | |||
JHHLHNBC_03514 | 1.9e-60 | |||||
JHHLHNBC_03515 | 4e-24 | L | NUMOD4 motif | |||
JHHLHNBC_03519 | 2.4e-35 | |||||
JHHLHNBC_03522 | 4.4e-196 | 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 | ||
JHHLHNBC_03523 | 4.5e-129 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
JHHLHNBC_03524 | 1.1e-149 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
JHHLHNBC_03525 | 0.0 | V | ABC transporter transmembrane region | |||
JHHLHNBC_03526 | 6.7e-276 | V | (ABC) transporter | |||
JHHLHNBC_03527 | 1.9e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
JHHLHNBC_03528 | 9.7e-61 | yitW | S | Iron-sulfur cluster assembly protein | ||
JHHLHNBC_03529 | 5.3e-141 | |||||
JHHLHNBC_03530 | 3.2e-175 | |||||
JHHLHNBC_03531 | 2.6e-263 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
JHHLHNBC_03532 | 9.5e-197 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
JHHLHNBC_03533 | 6.7e-127 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
JHHLHNBC_03534 | 1.5e-115 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
JHHLHNBC_03535 | 6e-171 | 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 | |
JHHLHNBC_03536 | 0.0 | KLT | serine threonine protein kinase | |||
JHHLHNBC_03537 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_03538 | 1e-60 | glnR | K | Transcriptional regulator | ||
JHHLHNBC_03539 | 5.3e-141 | yqeM | Q | Methyltransferase | ||
JHHLHNBC_03540 | 1.9e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
JHHLHNBC_03541 | 2.5e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
JHHLHNBC_03542 | 9.4e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
JHHLHNBC_03543 | 6.4e-48 | yhbY | J | RNA-binding protein | ||
JHHLHNBC_03544 | 1.8e-217 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
JHHLHNBC_03545 | 2.4e-95 | yqeG | S | HAD phosphatase, family IIIA | ||
JHHLHNBC_03546 | 1.7e-138 | 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 | ||
JHHLHNBC_03547 | 6.4e-60 | 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 | |
JHHLHNBC_03548 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
JHHLHNBC_03549 | 1.3e-104 | spl | M | NlpC/P60 family | ||
JHHLHNBC_03550 | 1.4e-242 | 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) | |
JHHLHNBC_03551 | 3.1e-170 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
JHHLHNBC_03552 | 1.7e-57 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
JHHLHNBC_03553 | 6.6e-173 | 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 | ||
JHHLHNBC_03554 | 0.0 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
JHHLHNBC_03555 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
JHHLHNBC_03556 | 1.1e-286 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
JHHLHNBC_03557 | 2.7e-208 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
JHHLHNBC_03558 | 1.9e-121 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
JHHLHNBC_03559 | 1.5e-115 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
JHHLHNBC_03560 | 5.1e-170 | 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 | |
JHHLHNBC_03561 | 0.0 | KLT | serine threonine protein kinase | |||
JHHLHNBC_03562 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_03563 | 9.8e-80 | F | Nucleoside 2-deoxyribosyltransferase | |||
JHHLHNBC_03564 | 5.7e-250 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
JHHLHNBC_03565 | 6e-64 | |||||
JHHLHNBC_03566 | 1.4e-130 | frvR | K | Mga helix-turn-helix domain | ||
JHHLHNBC_03567 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
JHHLHNBC_03568 | 4.7e-28 | |||||
JHHLHNBC_03569 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
JHHLHNBC_03570 | 5.5e-83 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
JHHLHNBC_03571 | 6.7e-270 | pipD | E | Dipeptidase | ||
JHHLHNBC_03572 | 2.9e-18 | |||||
JHHLHNBC_03573 | 1.3e-36 | |||||
JHHLHNBC_03574 | 7.5e-177 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
JHHLHNBC_03575 | 2.3e-122 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
JHHLHNBC_03576 | 6.1e-183 | vraS | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_03577 | 2.6e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_03578 | 3.6e-188 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
JHHLHNBC_03579 | 2.8e-99 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
JHHLHNBC_03580 | 1.8e-273 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
JHHLHNBC_03581 | 3.3e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
JHHLHNBC_03582 | 4.6e-252 | dnaB | L | replication initiation and membrane attachment | ||
JHHLHNBC_03583 | 4.9e-168 | dnaI | L | Primosomal protein DnaI | ||
JHHLHNBC_03584 | 1e-151 | glcU | U | sugar transport | ||
JHHLHNBC_03585 | 2.6e-109 | vanZ | V | VanZ like family | ||
JHHLHNBC_03586 | 3.3e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
JHHLHNBC_03587 | 1.3e-251 | dnaB | L | replication initiation and membrane attachment | ||
JHHLHNBC_03588 | 3.7e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
JHHLHNBC_03589 | 7.8e-174 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
JHHLHNBC_03590 | 1.5e-33 | |||||
JHHLHNBC_03591 | 4.8e-193 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
JHHLHNBC_03592 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
JHHLHNBC_03594 | 7.9e-217 | M | Glycosyl hydrolases family 25 | |||
JHHLHNBC_03595 | 3e-67 | S | Pfam:Phage_holin_6_1 | |||
JHHLHNBC_03596 | 6.6e-39 | |||||
JHHLHNBC_03598 | 7.6e-52 | |||||
JHHLHNBC_03599 | 0.0 | S | cellulase activity | |||
JHHLHNBC_03600 | 2.4e-231 | S | Phage tail protein | |||
JHHLHNBC_03601 | 1.2e-74 | sacB | GT2,GT4 | H | Stealth protein CR1, conserved region 1 | |
JHHLHNBC_03602 | 7.9e-84 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
JHHLHNBC_03603 | 4.9e-77 | cpsE | M | Bacterial sugar transferase | ||
JHHLHNBC_03604 | 9.7e-103 | L | Bacterial dnaA protein | |||
JHHLHNBC_03605 | 2.5e-180 | L | Integrase core domain | |||
JHHLHNBC_03606 | 1.1e-80 | L | Transposase DDE domain | |||
JHHLHNBC_03607 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
JHHLHNBC_03608 | 5.7e-183 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
JHHLHNBC_03609 | 2.8e-131 | 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 | |
JHHLHNBC_03610 | 4.3e-149 | S | haloacid dehalogenase-like hydrolase | |||
JHHLHNBC_03611 | 2.8e-44 | |||||
JHHLHNBC_03612 | 2e-14 | |||||
JHHLHNBC_03613 | 2.4e-136 | |||||
JHHLHNBC_03614 | 2.7e-224 | spiA | K | IrrE N-terminal-like domain | ||
JHHLHNBC_03615 | 9.6e-152 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
JHHLHNBC_03616 | 2e-126 | V | ABC transporter | |||
JHHLHNBC_03617 | 4.7e-208 | bacI | V | MacB-like periplasmic core domain | ||
JHHLHNBC_03618 | 3.2e-183 | |||||
JHHLHNBC_03619 | 0.0 | M | Leucine rich repeats (6 copies) | |||
JHHLHNBC_03620 | 4.7e-134 | sfsA | S | Belongs to the SfsA family | ||
JHHLHNBC_03621 | 2.2e-221 | gbuA | 3.6.3.32 | E | glycine betaine | |
JHHLHNBC_03622 | 0.0 | uvrA2 | L | ABC transporter | ||
JHHLHNBC_03623 | 1.5e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
JHHLHNBC_03624 | 6e-216 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
JHHLHNBC_03625 | 1.6e-118 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
JHHLHNBC_03626 | 4e-35 | |||||
JHHLHNBC_03627 | 5e-96 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
JHHLHNBC_03628 | 5.6e-14 | manY | G | PTS system | ||
JHHLHNBC_03629 | 1.1e-208 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
JHHLHNBC_03630 | 1.1e-197 | M | Glycosyltransferase like family 2 | |||
JHHLHNBC_03631 | 2.2e-159 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
JHHLHNBC_03632 | 3.4e-155 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
JHHLHNBC_03633 | 1.9e-107 | mntB | 3.6.3.35 | P | ABC transporter | |
JHHLHNBC_03634 | 4.7e-144 | mtsB | U | ABC 3 transport family | ||
JHHLHNBC_03635 | 2.4e-175 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_03636 | 2.3e-51 | czrA | K | Transcriptional regulator, ArsR family | ||
JHHLHNBC_03637 | 3.6e-90 | 2.5.1.105 | P | Cation efflux family | ||
JHHLHNBC_03638 | 4.2e-24 | |||||
JHHLHNBC_03639 | 0.0 | mco | Q | Multicopper oxidase | ||
JHHLHNBC_03640 | 2.2e-227 | EGP | Major Facilitator Superfamily | |||
JHHLHNBC_03641 | 3.2e-62 | |||||
JHHLHNBC_03642 | 0.0 | pacL | P | P-type ATPase | ||
JHHLHNBC_03643 | 1.3e-280 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
JHHLHNBC_03644 | 1.8e-10 | |||||
JHHLHNBC_03645 | 1.5e-138 | |||||
JHHLHNBC_03646 | 1e-246 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
JHHLHNBC_03647 | 8.1e-22 | S | Short C-terminal domain | |||
JHHLHNBC_03648 | 5.5e-214 | yqiG | C | Oxidoreductase | ||
JHHLHNBC_03649 | 9.6e-119 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
JHHLHNBC_03650 | 4.7e-182 | S | Aldo keto reductase | |||
JHHLHNBC_03652 | 3.8e-54 | S | Enterocin A Immunity | |||
JHHLHNBC_03653 | 1.4e-145 | S | Alpha beta hydrolase | |||
JHHLHNBC_03658 | 1.1e-22 | |||||
JHHLHNBC_03659 | 2.7e-138 | plnD | K | LytTr DNA-binding domain | ||
JHHLHNBC_03660 | 2.6e-111 | 2.7.13.3 | T | protein histidine kinase activity | ||
JHHLHNBC_03662 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
JHHLHNBC_03663 | 6.7e-222 | mesE | M | Transport protein ComB | ||
JHHLHNBC_03664 | 7.9e-252 | yjjP | S | Putative threonine/serine exporter | ||
JHHLHNBC_03665 | 1.7e-187 | tas | C | Aldo/keto reductase family | ||
JHHLHNBC_03667 | 9.6e-46 | S | Enterocin A Immunity | |||
JHHLHNBC_03668 | 8.4e-84 | |||||
JHHLHNBC_03669 | 1.8e-56 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_03670 | 7e-81 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_03671 | 2.1e-93 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_03672 | 4.3e-205 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
JHHLHNBC_03673 | 4.4e-230 | N | Uncharacterized conserved protein (DUF2075) | |||
JHHLHNBC_03674 | 1.5e-103 | |||||
JHHLHNBC_03675 | 5.5e-95 | |||||
JHHLHNBC_03676 | 8.4e-226 | V | regulation of methylation-dependent chromatin silencing | |||
JHHLHNBC_03677 | 4e-19 | |||||
JHHLHNBC_03678 | 3e-83 | ssuC2 | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_03679 | 6.1e-92 | P | ABC transporter | |||
JHHLHNBC_03680 | 3.6e-95 | P | ABC transporter, substratebinding protein | |||
JHHLHNBC_03681 | 3.5e-110 | |||||
JHHLHNBC_03682 | 1.3e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
JHHLHNBC_03683 | 6.7e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
JHHLHNBC_03684 | 3.2e-71 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
JHHLHNBC_03685 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
JHHLHNBC_03686 | 1.1e-231 | ymfF | S | Peptidase M16 inactive domain protein | ||
JHHLHNBC_03687 | 3.8e-219 | ymfH | S | Peptidase M16 | ||
JHHLHNBC_03688 | 2.8e-126 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
JHHLHNBC_03689 | 1.1e-78 | manR | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |
JHHLHNBC_03690 | 4.7e-148 | tatD | L | hydrolase, TatD family | ||
JHHLHNBC_03691 | 2.9e-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 | |
JHHLHNBC_03692 | 1.3e-157 | 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 | |
JHHLHNBC_03693 | 2.2e-51 | 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 | ||
JHHLHNBC_03694 | 0.0 | mngB | 3.2.1.170 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
JHHLHNBC_03695 | 1.5e-255 | S | Metal-independent alpha-mannosidase (GH125) | |||
JHHLHNBC_03696 | 2.5e-161 | ypbG | 2.7.1.2 | GK | ROK family | |
JHHLHNBC_03697 | 2.3e-297 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JHHLHNBC_03698 | 3.5e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_03699 | 6e-49 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_03700 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_03701 | 2.6e-112 | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | ||
JHHLHNBC_03702 | 1.1e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_03703 | 1.2e-45 | sgcB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_03704 | 5.1e-246 | G | PTS system sugar-specific permease component | |||
JHHLHNBC_03705 | 2.7e-224 | dgoD | 4.2.1.6 | M | Mandelate racemase muconate lactonizing enzyme | |
JHHLHNBC_03706 | 2.2e-89 | |||||
JHHLHNBC_03707 | 2.4e-248 | ypiB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_03708 | 1.8e-72 | K | Transcriptional regulator | |||
JHHLHNBC_03709 | 1.2e-76 | |||||
JHHLHNBC_03710 | 4.7e-160 | K | LysR substrate binding domain | |||
JHHLHNBC_03711 | 2.1e-247 | P | Sodium:sulfate symporter transmembrane region | |||
JHHLHNBC_03712 | 3.2e-101 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
JHHLHNBC_03713 | 4e-289 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
JHHLHNBC_03714 | 4.5e-149 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_03715 | 1e-129 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_03716 | 3e-162 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_03717 | 2.9e-256 | fucA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
JHHLHNBC_03718 | 1.2e-137 | K | UTRA domain | |||
JHHLHNBC_03719 | 1.8e-19 | |||||
JHHLHNBC_03720 | 3.5e-163 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_03721 | 1.8e-84 | |||||
JHHLHNBC_03722 | 9.3e-118 | GM | NmrA-like family | |||
JHHLHNBC_03723 | 3.8e-165 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_03724 | 6.2e-174 | shetA | P | Voltage-dependent anion channel | ||
JHHLHNBC_03725 | 1.1e-147 | rlrG | K | Transcriptional regulator | ||
JHHLHNBC_03726 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
JHHLHNBC_03728 | 1e-39 | celB | 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 | |
JHHLHNBC_03729 | 6e-117 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
JHHLHNBC_03730 | 3.6e-232 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
JHHLHNBC_03731 | 2.2e-128 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
JHHLHNBC_03732 | 1.1e-145 | p75 | M | NlpC P60 family protein | ||
JHHLHNBC_03733 | 1e-262 | nox | 1.6.3.4 | C | NADH oxidase | |
JHHLHNBC_03734 | 6.2e-162 | sepS16B | ||||
JHHLHNBC_03735 | 1.1e-119 | |||||
JHHLHNBC_03736 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
JHHLHNBC_03737 | 2.5e-101 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
JHHLHNBC_03738 | 3.3e-42 | rpmE2 | J | Ribosomal protein L31 | ||
JHHLHNBC_03739 | 1.3e-210 | 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 | |
JHHLHNBC_03740 | 9.2e-180 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
JHHLHNBC_03741 | 1e-81 | yjhE | S | Phage tail protein | ||
JHHLHNBC_03742 | 1.5e-173 | S | Cell surface protein | |||
JHHLHNBC_03743 | 1.1e-102 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_03744 | 1.9e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
JHHLHNBC_03745 | 5e-117 | |||||
JHHLHNBC_03746 | 1.4e-119 | tcyB | E | ABC transporter | ||
JHHLHNBC_03747 | 2.8e-143 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
JHHLHNBC_03748 | 3e-212 | metC | 4.4.1.8 | E | cystathionine | |
JHHLHNBC_03750 | 4.2e-141 | |||||
JHHLHNBC_03752 | 1.8e-50 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
JHHLHNBC_03753 | 8.5e-254 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
JHHLHNBC_03754 | 1.9e-100 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTPase | |
JHHLHNBC_03755 | 1.8e-303 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_03756 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
JHHLHNBC_03758 | 3.6e-18 | |||||
JHHLHNBC_03759 | 2.5e-256 | bmr3 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_03760 | 1.4e-138 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
JHHLHNBC_03761 | 6.7e-161 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase superfamily domain | |
JHHLHNBC_03762 | 2.5e-242 | sgaT | 2.7.1.194 | S | PTS system sugar-specific permease component | |
JHHLHNBC_03763 | 6.4e-162 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_03764 | 4.2e-286 | 2.7.1.12, 2.7.1.17, 2.7.1.5 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
JHHLHNBC_03765 | 3.2e-133 | K | DeoR C terminal sensor domain | |||
JHHLHNBC_03766 | 2.2e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
JHHLHNBC_03767 | 2.3e-281 | 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 | |
JHHLHNBC_03768 | 6.6e-125 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
JHHLHNBC_03769 | 1.7e-218 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
JHHLHNBC_03770 | 7.7e-138 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
JHHLHNBC_03771 | 0.0 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
JHHLHNBC_03772 | 8.6e-41 | sprD | D | Domain of Unknown Function (DUF1542) | ||
JHHLHNBC_03773 | 4e-309 | yknV | V | ABC transporter | ||
JHHLHNBC_03774 | 1.4e-141 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
JHHLHNBC_03775 | 9.6e-89 | S | CAAX protease self-immunity | |||
JHHLHNBC_03776 | 1.2e-213 | ulaG | S | Beta-lactamase superfamily domain | ||
JHHLHNBC_03777 | 3.2e-80 | 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 | |
JHHLHNBC_03778 | 5.3e-281 | ulaA | S | PTS system sugar-specific permease component | ||
JHHLHNBC_03779 | 3.7e-45 | sgaB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_03780 | 7.4e-115 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
JHHLHNBC_03781 | 4.9e-137 | repA | K | DeoR C terminal sensor domain | ||
JHHLHNBC_03782 | 2.1e-168 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
JHHLHNBC_03783 | 4.1e-150 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_03784 | 1.9e-135 | araD | 4.1.2.17, 4.1.2.19, 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 | |
JHHLHNBC_03785 | 1.5e-29 | yoeB | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | ||
JHHLHNBC_03786 | 2.5e-24 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
JHHLHNBC_03787 | 3.2e-97 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
JHHLHNBC_03788 | 2.1e-171 | |||||
JHHLHNBC_03790 | 1.3e-128 | cobB | K | Sir2 family | ||
JHHLHNBC_03791 | 3.4e-106 | yiiE | S | Protein of unknown function (DUF1211) | ||
JHHLHNBC_03792 | 3.3e-169 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
JHHLHNBC_03793 | 8e-90 | 3.6.1.55 | F | NUDIX domain | ||
JHHLHNBC_03794 | 2.1e-151 | yunF | F | Protein of unknown function DUF72 | ||
JHHLHNBC_03795 | 1.5e-129 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
JHHLHNBC_03796 | 4.2e-34 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
JHHLHNBC_03797 | 2.1e-127 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
JHHLHNBC_03798 | 6.8e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
JHHLHNBC_03799 | 1.3e-30 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
JHHLHNBC_03800 | 1.3e-154 | spo0J | K | Belongs to the ParB family | ||
JHHLHNBC_03801 | 4.3e-138 | soj | D | Sporulation initiation inhibitor | ||
JHHLHNBC_03802 | 8.5e-148 | noc | K | Belongs to the ParB family | ||
JHHLHNBC_03803 | 2.6e-132 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
JHHLHNBC_03804 | 6.8e-262 | 2.4.1.336 | GT2 | M | Glycosyl transferase | |
JHHLHNBC_03805 | 1.3e-66 | |||||
JHHLHNBC_03806 | 8e-128 | cobQ | S | glutamine amidotransferase | ||
JHHLHNBC_03807 | 1.2e-106 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
JHHLHNBC_03809 | 1.1e-26 | V | ABC transporter transmembrane region | |||
JHHLHNBC_03811 | 4e-15 | |||||
JHHLHNBC_03812 | 7.2e-86 | C | Radical SAM | |||
JHHLHNBC_03813 | 1.1e-10 | L | Transposase DDE domain group 1 | |||
JHHLHNBC_03815 | 7.4e-180 | ytgP | S | Polysaccharide biosynthesis protein | ||
JHHLHNBC_03816 | 1.3e-119 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
JHHLHNBC_03817 | 9.1e-151 | S | Protein of unknown function (DUF979) | |||
JHHLHNBC_03818 | 4.2e-116 | S | Protein of unknown function (DUF969) | |||
JHHLHNBC_03819 | 3.7e-70 | asp2 | S | Asp23 family, cell envelope-related function | ||
JHHLHNBC_03820 | 2.3e-69 | asp23 | S | Asp23 family, cell envelope-related function | ||
JHHLHNBC_03821 | 8.6e-30 | |||||
JHHLHNBC_03822 | 1.1e-87 | S | Protein conserved in bacteria | |||
JHHLHNBC_03823 | 1.3e-38 | S | Transglycosylase associated protein | |||
JHHLHNBC_03824 | 7e-71 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
JHHLHNBC_03825 | 1.1e-167 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
JHHLHNBC_03826 | 2.7e-28 | |||||
JHHLHNBC_03827 | 1.6e-38 | |||||
JHHLHNBC_03828 | 1.6e-82 | fld | C | Flavodoxin | ||
JHHLHNBC_03829 | 2.5e-52 | |||||
JHHLHNBC_03831 | 2.2e-150 | P | Belongs to the ABC transporter superfamily | |||
JHHLHNBC_03832 | 2.6e-150 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | |||
JHHLHNBC_03833 | 2.5e-95 | EP | N-terminal TM domain of oligopeptide transport permease C | |||
JHHLHNBC_03834 | 7.5e-108 | EP | Binding-protein-dependent transport system inner membrane component | |||
JHHLHNBC_03835 | 0.0 | ggt | 2.3.2.2, 3.4.19.13 | E | Gamma-glutamyltranspeptidase | |
JHHLHNBC_03836 | 1.6e-56 | ywjH | S | Protein of unknown function (DUF1634) | ||
JHHLHNBC_03837 | 1.3e-135 | yxaA | S | Sulfite exporter TauE/SafE | ||
JHHLHNBC_03838 | 8e-225 | S | TPM domain | |||
JHHLHNBC_03839 | 2e-117 | |||||
JHHLHNBC_03840 | 1e-259 | nox | C | NADH oxidase | ||
JHHLHNBC_03841 | 9.9e-186 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
JHHLHNBC_03842 | 4.7e-227 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
JHHLHNBC_03843 | 9.2e-104 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
JHHLHNBC_03844 | 5.3e-130 | ymfM | S | Helix-turn-helix domain | ||
JHHLHNBC_03845 | 1.1e-92 | K | Cro/C1-type HTH DNA-binding domain | |||
JHHLHNBC_03846 | 1e-227 | steT | E | Amino acid permease | ||
JHHLHNBC_03847 | 1.1e-138 | puuD | S | peptidase C26 | ||
JHHLHNBC_03848 | 1.1e-80 | |||||
JHHLHNBC_03849 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
JHHLHNBC_03850 | 7.5e-83 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_03851 | 4.9e-132 | S | Protein of unknown function C-terminus (DUF2399) | |||
JHHLHNBC_03852 | 0.0 | D | Putative exonuclease SbcCD, C subunit | |||
JHHLHNBC_03853 | 2.6e-46 | D | Putative exonuclease SbcCD, C subunit | |||
JHHLHNBC_03854 | 1.6e-180 | |||||
JHHLHNBC_03855 | 2.5e-275 | |||||
JHHLHNBC_03856 | 6.3e-157 | yvfR | V | ABC transporter | ||
JHHLHNBC_03857 | 8.2e-129 | yvfS | V | ABC-2 type transporter | ||
JHHLHNBC_03858 | 6.4e-199 | desK | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_03859 | 1.1e-102 | desR | K | helix_turn_helix, Lux Regulon | ||
JHHLHNBC_03860 | 1.1e-115 | |||||
JHHLHNBC_03861 | 2.8e-154 | S | Uncharacterised protein, DegV family COG1307 | |||
JHHLHNBC_03862 | 2.2e-84 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_03863 | 3.3e-158 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_03864 | 1.9e-88 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
JHHLHNBC_03865 | 1.6e-97 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
JHHLHNBC_03866 | 7.1e-34 | K | Psort location Cytoplasmic, score | |||
JHHLHNBC_03867 | 6.1e-37 | K | Psort location Cytoplasmic, score | |||
JHHLHNBC_03868 | 7.9e-36 | |||||
JHHLHNBC_03869 | 2.1e-54 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
JHHLHNBC_03870 | 3.6e-78 | yphH | S | Cupin domain | ||
JHHLHNBC_03871 | 1.6e-160 | K | Transcriptional regulator | |||
JHHLHNBC_03872 | 1.4e-128 | S | ABC-2 family transporter protein | |||
JHHLHNBC_03873 | 4.1e-167 | bcrA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
JHHLHNBC_03874 | 1.2e-120 | T | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_03875 | 7.6e-150 | T | GHKL domain | |||
JHHLHNBC_03876 | 0.0 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_03877 | 2.6e-157 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
JHHLHNBC_03878 | 8.9e-133 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
JHHLHNBC_03879 | 3.5e-137 | pnuC | H | nicotinamide mononucleotide transporter | ||
JHHLHNBC_03880 | 1.1e-164 | IQ | NAD dependent epimerase/dehydratase family | |||
JHHLHNBC_03881 | 2.8e-154 | 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 | |
JHHLHNBC_03882 | 9.9e-39 | ylqC | S | Belongs to the UPF0109 family | ||
JHHLHNBC_03883 | 2.9e-93 | 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 | ||
JHHLHNBC_03884 | 1e-142 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
JHHLHNBC_03885 | 1.9e-127 | 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 | ||
JHHLHNBC_03886 | 4.3e-104 | 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 | ||
JHHLHNBC_03887 | 1.6e-137 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JHHLHNBC_03888 | 6.9e-96 | 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 | |||
JHHLHNBC_03889 | 8.5e-38 | fer | C | 4Fe-4S single cluster domain of Ferredoxin I | ||
JHHLHNBC_03890 | 6.1e-177 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
JHHLHNBC_03891 | 6.7e-270 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
JHHLHNBC_03892 | 2.3e-50 | M | Lysin motif | |||
JHHLHNBC_03893 | 1.7e-114 | 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 | |
JHHLHNBC_03894 | 0.0 | scrA | 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_03895 | 0.0 | pip | V | domain protein | ||
JHHLHNBC_03896 | 1.4e-212 | ykiI | ||||
JHHLHNBC_03897 | 5.3e-94 | |||||
JHHLHNBC_03898 | 6.7e-29 | S | MazG-like family | |||
JHHLHNBC_03899 | 5.8e-173 | S | Uncharacterized conserved protein (DUF2075) | |||
JHHLHNBC_03900 | 3.4e-132 | dcm | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
JHHLHNBC_03901 | 6.5e-146 | S | Domain of unknown function (DUF1998) | |||
JHHLHNBC_03902 | 1.9e-281 | KL | Helicase conserved C-terminal domain | |||
JHHLHNBC_03905 | 1.5e-129 | 2.7.1.202 | K | PRD domain | ||
JHHLHNBC_03906 | 2.1e-32 | ulaB_1 | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_03907 | 7.2e-178 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
JHHLHNBC_03908 | 1.2e-280 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
JHHLHNBC_03909 | 1.9e-78 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_03910 | 3.5e-118 | G | PTS system mannose fructose sorbose family | |||
JHHLHNBC_03911 | 2e-38 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_03912 | 7.7e-28 | 2.7.1.191 | G | PTS system fructose IIA component | ||
JHHLHNBC_03913 | 2.5e-79 | 1.1.1.399, 1.1.1.95 | C | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | ||
JHHLHNBC_03914 | 5.3e-57 | eda | 4.1.2.14, 4.1.3.42 | G | 2-dehydro-3-deoxyphosphogluconate aldolase 4-hydroxy-2-oxoglutarate aldolase | |
JHHLHNBC_03915 | 7.9e-17 | |||||
JHHLHNBC_03916 | 1.7e-50 | gntR | K | rpiR family | ||
JHHLHNBC_03917 | 8.3e-22 | chpR | T | PFAM SpoVT AbrB | ||
JHHLHNBC_03918 | 8.7e-221 | F | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
JHHLHNBC_03919 | 7.6e-205 | S | Protein of unknown function (DUF917) | |||
JHHLHNBC_03920 | 5.6e-286 | apc3 | 3.5.2.9 | EQ | Hydantoinase/oxoprolinase N-terminal region | |
JHHLHNBC_03921 | 1.9e-144 | frlD | 2.7.1.218 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_03922 | 1.5e-104 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_03923 | 5.6e-73 | V | CAAX protease self-immunity | |||
JHHLHNBC_03924 | 2.2e-108 | |||||
JHHLHNBC_03925 | 0.0 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
JHHLHNBC_03926 | 1.6e-146 | thrC | 4.2.3.1 | E | Threonine synthase | |
JHHLHNBC_03927 | 9.2e-223 | mdtG | EGP | Major facilitator Superfamily | ||
JHHLHNBC_03928 | 5e-92 | K | acetyltransferase | |||
JHHLHNBC_03929 | 1.3e-93 | |||||
JHHLHNBC_03930 | 8.5e-221 | yceI | G | Sugar (and other) transporter | ||
JHHLHNBC_03931 | 2.8e-217 | |||||
JHHLHNBC_03932 | 2.1e-290 | 2.4.1.52 | GT4 | M | Poly(Glycerol-phosphate) alpha-glucosyltransferase | |
JHHLHNBC_03933 | 3.3e-302 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
JHHLHNBC_03934 | 1.5e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
JHHLHNBC_03935 | 1e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
JHHLHNBC_03937 | 4.8e-291 | V | ABC transporter transmembrane region | |||
JHHLHNBC_03938 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
JHHLHNBC_03939 | 4.4e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
JHHLHNBC_03940 | 6.4e-138 | 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 | ||
JHHLHNBC_03941 | 1.9e-59 | 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 | |
JHHLHNBC_03944 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
JHHLHNBC_03945 | 2.4e-14 | |||||
JHHLHNBC_03946 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
JHHLHNBC_03947 | 7.2e-56 | ysxB | J | Cysteine protease Prp | ||
JHHLHNBC_03948 | 5e-145 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
JHHLHNBC_03949 | 1.4e-46 | yktA | S | Belongs to the UPF0223 family | ||
JHHLHNBC_03950 | 5.4e-156 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
JHHLHNBC_03951 | 1.5e-258 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
JHHLHNBC_03952 | 1.4e-242 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
JHHLHNBC_03953 | 3.1e-130 | yrjD | S | LUD domain | ||
JHHLHNBC_03954 | 3.1e-289 | lutB | C | 4Fe-4S dicluster domain | ||
JHHLHNBC_03955 | 9.5e-149 | lutA | C | Cysteine-rich domain | ||
JHHLHNBC_03956 | 2.2e-102 | |||||
JHHLHNBC_03957 | 9.5e-53 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_03958 | 5.5e-211 | S | Bacterial protein of unknown function (DUF871) | |||
JHHLHNBC_03959 | 2.7e-70 | S | Domain of unknown function (DUF3284) | |||
JHHLHNBC_03960 | 4e-270 | celB | 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 | |
JHHLHNBC_03961 | 1e-259 | nox | 1.6.3.4 | C | NADH oxidase | |
JHHLHNBC_03962 | 2.9e-151 | sepS16B | ||||
JHHLHNBC_03963 | 1.1e-119 | |||||
JHHLHNBC_03964 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
JHHLHNBC_03965 | 9.1e-23 | L | Helix-turn-helix domain | |||
JHHLHNBC_03966 | 1.6e-52 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
JHHLHNBC_03967 | 7.5e-225 | 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 | |
JHHLHNBC_03968 | 8.5e-184 | 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 | |
JHHLHNBC_03969 | 6.6e-134 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
JHHLHNBC_03970 | 4.4e-47 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
JHHLHNBC_03971 | 0.0 | clpB | 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 | ||
JHHLHNBC_03972 | 9.2e-37 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
JHHLHNBC_03973 | 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 | ||
JHHLHNBC_03974 | 4.6e-58 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
JHHLHNBC_03975 | 1.5e-141 | terC | P | membrane | ||
JHHLHNBC_03976 | 1.7e-165 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
JHHLHNBC_03977 | 1.3e-176 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
JHHLHNBC_03978 | 1.1e-225 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
JHHLHNBC_03980 | 8.4e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
JHHLHNBC_03981 | 1.4e-99 | 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 | ||
JHHLHNBC_03982 | 1e-286 | dnaK | O | Heat shock 70 kDa protein | ||
JHHLHNBC_03983 | 4.1e-188 | 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 | ||
JHHLHNBC_03984 | 2.9e-277 | V | ABC transporter transmembrane region | |||
JHHLHNBC_03985 | 1.9e-110 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
JHHLHNBC_03986 | 3.6e-67 | K | MarR family | |||
JHHLHNBC_03987 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
JHHLHNBC_03988 | 7.9e-129 | S | Belongs to the UPF0246 family | |||
JHHLHNBC_03989 | 5.3e-127 | |||||
JHHLHNBC_03990 | 5.4e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
JHHLHNBC_03991 | 2.4e-245 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
JHHLHNBC_03992 | 1.1e-203 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
JHHLHNBC_03993 | 9.6e-242 | pbuX | F | xanthine permease | ||
JHHLHNBC_03994 | 1.2e-100 | 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 | |
JHHLHNBC_03995 | 1.6e-109 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
JHHLHNBC_03996 | 8.1e-82 | yvbK | 3.1.3.25 | K | GNAT family | |
JHHLHNBC_03997 | 9.8e-28 | chpR | T | PFAM SpoVT AbrB | ||
JHHLHNBC_03998 | 2.1e-31 | cspC | K | Cold shock protein | ||
JHHLHNBC_03999 | 8.6e-168 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
JHHLHNBC_04000 | 2.1e-109 | |||||
JHHLHNBC_04001 | 4.3e-172 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
JHHLHNBC_04002 | 1.6e-83 | S | Fic/DOC family | |||
JHHLHNBC_04003 | 9.6e-303 | S | Psort location CytoplasmicMembrane, score | |||
JHHLHNBC_04004 | 0.0 | S | Bacterial membrane protein YfhO | |||
JHHLHNBC_04005 | 3.3e-309 | bglH | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_04006 | 4.1e-294 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
JHHLHNBC_04007 | 1.4e-97 | N | domain, Protein | |||
JHHLHNBC_04008 | 4.7e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
JHHLHNBC_04009 | 3e-276 | |||||
JHHLHNBC_04010 | 1.6e-160 | V | ABC transporter | |||
JHHLHNBC_04011 | 1.2e-82 | FG | adenosine 5'-monophosphoramidase activity | |||
JHHLHNBC_04012 | 2.3e-248 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
JHHLHNBC_04013 | 9.8e-91 | 3.1.3.18 | J | HAD-hyrolase-like | ||
JHHLHNBC_04014 | 0.0 | yebA | E | Transglutaminase/protease-like homologues | ||
JHHLHNBC_04015 | 1.2e-158 | yeaD | S | Protein of unknown function DUF58 | ||
JHHLHNBC_04016 | 1.5e-169 | yeaC | S | ATPase family associated with various cellular activities (AAA) | ||
JHHLHNBC_04017 | 6.7e-105 | S | Stage II sporulation protein M | |||
JHHLHNBC_04018 | 1.2e-100 | ydaF | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_04019 | 4.7e-266 | glnP | P | ABC transporter | ||
JHHLHNBC_04020 | 6.5e-257 | glnP | P | ABC transporter | ||
JHHLHNBC_04021 | 2.6e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_04022 | 2.4e-169 | yniA | G | Phosphotransferase enzyme family | ||
JHHLHNBC_04023 | 3.7e-145 | S | AAA ATPase domain | |||
JHHLHNBC_04024 | 1.3e-287 | ydbT | S | Bacterial PH domain | ||
JHHLHNBC_04025 | 8.7e-81 | S | Bacterial PH domain | |||
JHHLHNBC_04026 | 1.2e-52 | |||||
JHHLHNBC_04027 | 1.5e-58 | yqkB | S | Iron-sulphur cluster biosynthesis | ||
JHHLHNBC_04028 | 5.1e-133 | S | Protein of unknown function (DUF975) | |||
JHHLHNBC_04029 | 2.2e-251 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
JHHLHNBC_04030 | 0.0 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
JHHLHNBC_04031 | 3.3e-172 | 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 | ||
JHHLHNBC_04032 | 1.4e-53 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
JHHLHNBC_04033 | 6.4e-160 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
JHHLHNBC_04034 | 2.7e-241 | 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) | |
JHHLHNBC_04036 | 3.2e-62 | yfiC | V | ABC transporter | ||
JHHLHNBC_04037 | 6.6e-139 | S | NADPH-dependent FMN reductase | |||
JHHLHNBC_04038 | 2.3e-164 | 1.13.11.2 | S | glyoxalase | ||
JHHLHNBC_04039 | 3.1e-192 | ampC | V | Beta-lactamase | ||
JHHLHNBC_04040 | 2.5e-149 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
JHHLHNBC_04041 | 2.3e-148 | DegV | S | EDD domain protein, DegV family | ||
JHHLHNBC_04042 | 9.6e-115 | hly | S | protein, hemolysin III | ||
JHHLHNBC_04043 | 6.7e-92 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
JHHLHNBC_04044 | 1.4e-86 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
JHHLHNBC_04045 | 4.6e-307 | 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 | ||
JHHLHNBC_04046 | 8.5e-184 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
JHHLHNBC_04047 | 1.2e-243 | els | S | Sterol carrier protein domain | ||
JHHLHNBC_04048 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
JHHLHNBC_04049 | 1.1e-116 | S | Repeat protein | |||
JHHLHNBC_04050 | 1.4e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
JHHLHNBC_04051 | 3.1e-68 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
JHHLHNBC_04052 | 1.5e-83 | M | Protein of unknown function (DUF3737) | |||
JHHLHNBC_04053 | 4e-133 | cobB | K | Sir2 family | ||
JHHLHNBC_04054 | 1.1e-62 | pcaC | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
JHHLHNBC_04055 | 7.9e-64 | rmeD | K | helix_turn_helix, mercury resistance | ||
JHHLHNBC_04056 | 1.4e-101 | 3.2.2.20 | K | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_04057 | 5.3e-92 | yxjI | ||||
JHHLHNBC_04058 | 2.8e-144 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_04059 | 8.4e-125 | 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 | |
JHHLHNBC_04060 | 2e-180 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
JHHLHNBC_04061 | 2e-82 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
JHHLHNBC_04062 | 2e-166 | natA | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04063 | 4.5e-217 | ysdA | CP | ABC-2 family transporter protein | ||
JHHLHNBC_04064 | 2.3e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04065 | 3.9e-11 | |||||
JHHLHNBC_04067 | 3e-145 | F | DNA RNA non-specific endonuclease | |||
JHHLHNBC_04068 | 4.8e-44 | yhiD | S | MgtC family | ||
JHHLHNBC_04069 | 2.5e-56 | |||||
JHHLHNBC_04070 | 1.4e-240 | |||||
JHHLHNBC_04071 | 1.9e-92 | |||||
JHHLHNBC_04072 | 5.2e-161 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
JHHLHNBC_04073 | 3.8e-215 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
JHHLHNBC_04074 | 5.3e-242 | ynbB | 4.4.1.1 | P | aluminum resistance | |
JHHLHNBC_04075 | 4.7e-182 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
JHHLHNBC_04076 | 4.4e-25 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
JHHLHNBC_04077 | 3.7e-72 | yqhL | P | Rhodanese-like protein | ||
JHHLHNBC_04078 | 2.4e-178 | glk | 2.7.1.2 | G | Glucokinase | |
JHHLHNBC_04079 | 1.1e-40 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
JHHLHNBC_04080 | 8.7e-122 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
JHHLHNBC_04081 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
JHHLHNBC_04082 | 3.7e-246 | amt | P | ammonium transporter | ||
JHHLHNBC_04083 | 1.5e-161 | 3.5.1.10 | C | nadph quinone reductase | ||
JHHLHNBC_04084 | 1.2e-57 | |||||
JHHLHNBC_04085 | 2.2e-51 | ybjQ | S | Belongs to the UPF0145 family | ||
JHHLHNBC_04086 | 4.9e-119 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
JHHLHNBC_04087 | 4.1e-144 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
JHHLHNBC_04088 | 0.0 | yjcE | P | Sodium proton antiporter | ||
JHHLHNBC_04090 | 1.4e-258 | S | Protein of unknown function (DUF3800) | |||
JHHLHNBC_04091 | 1.8e-254 | yifK | E | Amino acid permease | ||
JHHLHNBC_04092 | 4.9e-159 | yeaE | S | Aldo/keto reductase family | ||
JHHLHNBC_04093 | 5.1e-113 | ylbE | GM | NAD(P)H-binding | ||
JHHLHNBC_04094 | 9.5e-275 | lsa | S | ABC transporter | ||
JHHLHNBC_04095 | 2.7e-76 | O | OsmC-like protein | |||
JHHLHNBC_04096 | 1.2e-68 | |||||
JHHLHNBC_04097 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
JHHLHNBC_04098 | 2.1e-53 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
JHHLHNBC_04099 | 1.2e-16 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
JHHLHNBC_04100 | 3.5e-76 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
JHHLHNBC_04101 | 9.1e-121 | XK27_06930 | V | domain protein | ||
JHHLHNBC_04102 | 2.4e-67 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04104 | 2.9e-69 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
JHHLHNBC_04105 | 1.1e-91 | S | Alpha/beta hydrolase family | |||
JHHLHNBC_04106 | 3.2e-127 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
JHHLHNBC_04107 | 6.2e-67 | E | lactoylglutathione lyase activity | |||
JHHLHNBC_04108 | 1.8e-278 | 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) | |
JHHLHNBC_04109 | 9.7e-17 | yegS | 2.7.1.107 | G | Lipid kinase | |
JHHLHNBC_04110 | 1.8e-173 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
JHHLHNBC_04111 | 4.4e-155 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
JHHLHNBC_04112 | 7.2e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
JHHLHNBC_04113 | 5.3e-113 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
JHHLHNBC_04114 | 2.5e-102 | V | CAAX protease self-immunity | |||
JHHLHNBC_04115 | 1.1e-165 | shetA | P | Voltage-dependent anion channel | ||
JHHLHNBC_04116 | 1.6e-146 | rlrG | K | Transcriptional regulator | ||
JHHLHNBC_04117 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
JHHLHNBC_04118 | 6.6e-279 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
JHHLHNBC_04119 | 4.7e-174 | proV | E | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04120 | 2e-255 | gshR | 1.8.1.7 | C | Glutathione reductase | |
JHHLHNBC_04121 | 2.6e-191 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_04122 | 4.7e-103 | lemA | S | LemA family | ||
JHHLHNBC_04123 | 4.6e-112 | S | TPM domain | |||
JHHLHNBC_04124 | 3.5e-239 | dinF | V | MatE | ||
JHHLHNBC_04125 | 7.5e-91 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
JHHLHNBC_04126 | 7.9e-154 | bioC | 2.1.1.187, 2.1.1.197 | Q | Protein-L-isoaspartate(D-aspartate) O-methyltransferase (PCMT) | |
JHHLHNBC_04127 | 1.5e-283 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
JHHLHNBC_04128 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
JHHLHNBC_04129 | 2.8e-171 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
JHHLHNBC_04130 | 4.4e-159 | ypuA | S | Protein of unknown function (DUF1002) | ||
JHHLHNBC_04131 | 2.4e-25 | |||||
JHHLHNBC_04132 | 6.9e-68 | yodB | K | Transcriptional regulator, HxlR family | ||
JHHLHNBC_04133 | 5.6e-94 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
JHHLHNBC_04134 | 5.9e-88 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
JHHLHNBC_04135 | 2.5e-170 | mleP | S | Sodium Bile acid symporter family | ||
JHHLHNBC_04136 | 0.0 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
JHHLHNBC_04137 | 4.5e-163 | mleR | K | LysR family | ||
JHHLHNBC_04138 | 1e-173 | corA | P | CorA-like Mg2+ transporter protein | ||
JHHLHNBC_04139 | 6.7e-62 | yeaO | S | Protein of unknown function, DUF488 | ||
JHHLHNBC_04140 | 1.1e-98 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
JHHLHNBC_04141 | 1.9e-103 | |||||
JHHLHNBC_04142 | 7.1e-107 | ywrF | S | Flavin reductase like domain | ||
JHHLHNBC_04143 | 2e-164 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
JHHLHNBC_04144 | 3.8e-55 | |||||
JHHLHNBC_04145 | 2.1e-98 | 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 | |
JHHLHNBC_04146 | 1.4e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
JHHLHNBC_04147 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
JHHLHNBC_04148 | 4.6e-200 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
JHHLHNBC_04149 | 4.3e-115 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
JHHLHNBC_04150 | 1.3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
JHHLHNBC_04151 | 9.7e-100 | yqaB | S | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_04152 | 8.1e-08 | |||||
JHHLHNBC_04153 | 3.1e-159 | holB | 2.7.7.7 | L | DNA polymerase III | |
JHHLHNBC_04154 | 3.3e-110 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
JHHLHNBC_04155 | 9.5e-209 | yaaN | P | Toxic anion resistance protein (TelA) | ||
JHHLHNBC_04156 | 3.6e-263 | ydiC1 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_04157 | 5.1e-146 | pstS | P | Phosphate | ||
JHHLHNBC_04158 | 2.4e-36 | cspA | K | Cold shock protein | ||
JHHLHNBC_04159 | 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) | |
JHHLHNBC_04160 | 6.9e-84 | 3.4.23.43 | ||||
JHHLHNBC_04161 | 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 | |
JHHLHNBC_04162 | 3.7e-258 | 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) | |
JHHLHNBC_04163 | 4.3e-261 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
JHHLHNBC_04164 | 2.6e-13 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_04165 | 1e-273 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
JHHLHNBC_04166 | 2.9e-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) | ||
JHHLHNBC_04167 | 5.4e-144 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
JHHLHNBC_04168 | 5.3e-98 | yacP | S | YacP-like NYN domain | ||
JHHLHNBC_04170 | 1e-110 | K | Psort location Cytoplasmic, score | |||
JHHLHNBC_04171 | 4.8e-165 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
JHHLHNBC_04172 | 2.3e-167 | |||||
JHHLHNBC_04175 | 2.1e-23 | |||||
JHHLHNBC_04178 | 1.8e-83 | nosF | S | ATPase activity | ||
JHHLHNBC_04179 | 4.7e-191 | XK27_00915 | C | Luciferase-like monooxygenase | ||
JHHLHNBC_04180 | 2.7e-123 | 1.5.1.40 | S | Rossmann-like domain | ||
JHHLHNBC_04181 | 3.7e-32 | |||||
JHHLHNBC_04183 | 3e-160 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JHHLHNBC_04185 | 8.8e-116 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
JHHLHNBC_04186 | 3.8e-179 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_04187 | 2e-290 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
JHHLHNBC_04188 | 3.6e-215 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
JHHLHNBC_04189 | 0.0 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
JHHLHNBC_04190 | 2e-294 | uxuT | G | MFS/sugar transport protein | ||
JHHLHNBC_04191 | 1.7e-60 | |||||
JHHLHNBC_04192 | 2.1e-272 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
JHHLHNBC_04193 | 1.9e-218 | G | Major Facilitator | |||
JHHLHNBC_04195 | 2.7e-31 | K | PFAM GntR | |||
JHHLHNBC_04196 | 1.7e-134 | rspB | 1.1.1.380 | E | Alcohol dehydrogenase GroES-like domain | |
JHHLHNBC_04198 | 1.8e-127 | kdgR | K | FCD domain | ||
JHHLHNBC_04199 | 2e-191 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_04200 | 0.0 | M | Glycosyl hydrolase family 59 | |||
JHHLHNBC_04201 | 8.9e-170 | scrB | 3.2.1.26 | GH32 | G | beta-fructofuranosidase activity |
JHHLHNBC_04202 | 1.9e-237 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04203 | 4.6e-52 | K | TRANSCRIPTIONal | |||
JHHLHNBC_04204 | 0.0 | ydgH | S | MMPL family | ||
JHHLHNBC_04205 | 1.5e-106 | K | Tetracycline repressor, C-terminal all-alpha domain | |||
JHHLHNBC_04206 | 5.1e-37 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
JHHLHNBC_04207 | 4.4e-163 | K | LysR substrate binding domain | |||
JHHLHNBC_04208 | 3.6e-257 | S | Sulphur transport | |||
JHHLHNBC_04209 | 0.0 | naoX | P | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
JHHLHNBC_04210 | 2.9e-142 | tauC | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_04211 | 2.6e-183 | tauA | P | NMT1-like family | ||
JHHLHNBC_04212 | 5.4e-138 | tauB | 3.6.3.36 | P | ATPases associated with a variety of cellular activities | |
JHHLHNBC_04215 | 9.6e-55 | S | DsrE/DsrF-like family | |||
JHHLHNBC_04216 | 1.4e-254 | pbuO | S | permease | ||
JHHLHNBC_04217 | 3e-54 | S | Protein of unknown function (DUF1516) | |||
JHHLHNBC_04218 | 8.1e-58 | ypaA | S | Protein of unknown function (DUF1304) | ||
JHHLHNBC_04219 | 5.9e-43 | |||||
JHHLHNBC_04220 | 1.5e-132 | K | UTRA | |||
JHHLHNBC_04221 | 3.2e-291 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JHHLHNBC_04222 | 7.2e-253 | celD | 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 | |
JHHLHNBC_04223 | 6.1e-85 | |||||
JHHLHNBC_04224 | 2.6e-52 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
JHHLHNBC_04225 | 4.5e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_04226 | 1.1e-192 | ldhD3 | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
JHHLHNBC_04227 | 2e-91 | ogt | 2.1.1.63 | L | Methyltransferase | |
JHHLHNBC_04228 | 1.6e-120 | K | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_04229 | 3.5e-202 | T | PhoQ Sensor | |||
JHHLHNBC_04230 | 2.5e-86 | |||||
JHHLHNBC_04231 | 1.5e-65 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
JHHLHNBC_04232 | 1.8e-63 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
JHHLHNBC_04233 | 9.5e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
JHHLHNBC_04234 | 3.1e-150 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
JHHLHNBC_04235 | 1.9e-55 | |||||
JHHLHNBC_04236 | 4.2e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
JHHLHNBC_04237 | 1e-60 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
JHHLHNBC_04238 | 3.9e-159 | ytrB | V | ABC transporter | ||
JHHLHNBC_04239 | 1e-193 | |||||
JHHLHNBC_04240 | 3.7e-196 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JHHLHNBC_04241 | 4.2e-110 | ydiL | S | CAAX protease self-immunity | ||
JHHLHNBC_04242 | 0.0 | scrA | 2.7.1.211 | G | phosphotransferase system | |
JHHLHNBC_04243 | 0.0 | pip | V | domain protein | ||
JHHLHNBC_04244 | 3.1e-212 | ykiI | ||||
JHHLHNBC_04245 | 4.6e-103 | S | Putative inner membrane protein (DUF1819) | |||
JHHLHNBC_04246 | 4.7e-92 | S | Domain of unknown function (DUF1788) | |||
JHHLHNBC_04247 | 6.6e-75 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
JHHLHNBC_04248 | 9.6e-68 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_04249 | 3.9e-110 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
JHHLHNBC_04250 | 8.2e-09 | |||||
JHHLHNBC_04251 | 2.8e-84 | zur | P | Belongs to the Fur family | ||
JHHLHNBC_04253 | 1.5e-175 | |||||
JHHLHNBC_04254 | 9e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_04255 | 2.5e-147 | glnH | ET | ABC transporter substrate-binding protein | ||
JHHLHNBC_04256 | 2e-107 | gluC | P | ABC transporter permease | ||
JHHLHNBC_04257 | 1.5e-110 | glnP | P | ABC transporter permease | ||
JHHLHNBC_04258 | 1.2e-174 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
JHHLHNBC_04259 | 7.5e-135 | tuaG | GT2 | M | Glycosyltransferase like family 2 | |
JHHLHNBC_04260 | 2.1e-145 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
JHHLHNBC_04261 | 1e-257 | wcaJ | M | Bacterial sugar transferase | ||
JHHLHNBC_04262 | 1.2e-118 | |||||
JHHLHNBC_04263 | 1e-212 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
JHHLHNBC_04264 | 2.1e-185 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
JHHLHNBC_04265 | 2.6e-141 | icaC | M | Acyltransferase family | ||
JHHLHNBC_04266 | 4.4e-203 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
JHHLHNBC_04267 | 0.0 | M | Glycosyl hydrolases family 25 | |||
JHHLHNBC_04268 | 6e-236 | S | Bacterial membrane protein, YfhO | |||
JHHLHNBC_04269 | 4.1e-78 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
JHHLHNBC_04270 | 4.2e-39 | spr | 3.4.17.13 | M | NlpC/P60 family | |
JHHLHNBC_04271 | 6.4e-73 | S | Psort location CytoplasmicMembrane, score | |||
JHHLHNBC_04272 | 4.9e-139 | tagF | 2.7.8.12 | M | Glycosyl transferase, family 2 | |
JHHLHNBC_04273 | 1.6e-221 | M | Glycosyl transferases group 1 | |||
JHHLHNBC_04274 | 4.2e-259 | S | polysaccharide biosynthetic process | |||
JHHLHNBC_04275 | 1e-114 | ywqC | M | capsule polysaccharide biosynthetic process | ||
JHHLHNBC_04276 | 1.2e-104 | epsG | 2.7.10.1 | D | Capsular exopolysaccharide family | |
JHHLHNBC_04277 | 1.3e-185 | S | EpsG family | |||
JHHLHNBC_04278 | 0.0 | M | Sulfatase | |||
JHHLHNBC_04279 | 3.7e-150 | nodB3 | G | Polysaccharide deacetylase | ||
JHHLHNBC_04280 | 4.2e-234 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
JHHLHNBC_04281 | 1.4e-164 | yegS | I | Diacylglycerol kinase catalytic domain | ||
JHHLHNBC_04282 | 0.0 | E | Amino acid permease | |||
JHHLHNBC_04283 | 5.3e-136 | cysA | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04284 | 0.0 | V | FtsX-like permease family | |||
JHHLHNBC_04285 | 1.2e-176 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
JHHLHNBC_04286 | 4.2e-129 | pgm3 | G | Phosphoglycerate mutase family | ||
JHHLHNBC_04287 | 8.3e-187 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
JHHLHNBC_04288 | 3.7e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
JHHLHNBC_04289 | 1e-81 | yjhE | S | Phage tail protein | ||
JHHLHNBC_04290 | 1.2e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
JHHLHNBC_04291 | 5.4e-271 | V | ABC transporter transmembrane region | |||
JHHLHNBC_04292 | 3.5e-18 | K | sequence-specific DNA binding | |||
JHHLHNBC_04293 | 1.5e-150 | EG | EamA-like transporter family | |||
JHHLHNBC_04294 | 1.2e-70 | 3.6.1.55 | L | NUDIX domain | ||
JHHLHNBC_04296 | 2e-43 | K | Helix-turn-helix domain | |||
JHHLHNBC_04298 | 8.3e-54 | S | Protein conserved in bacteria | |||
JHHLHNBC_04299 | 1e-122 | V | ABC transporter | |||
JHHLHNBC_04301 | 1.8e-10 | H | Methyltransferase domain | |||
JHHLHNBC_04302 | 1.5e-25 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04303 | 5.2e-25 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04304 | 1.8e-101 | 2.7.7.80 | H | ThiF family | ||
JHHLHNBC_04305 | 9.9e-42 | S | ThiS family | |||
JHHLHNBC_04306 | 1.3e-196 | 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 | |
JHHLHNBC_04307 | 1.3e-187 | 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 | |
JHHLHNBC_04308 | 3.5e-263 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
JHHLHNBC_04309 | 3.5e-244 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
JHHLHNBC_04310 | 3e-69 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
JHHLHNBC_04311 | 1.1e-217 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
JHHLHNBC_04312 | 7.6e-166 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
JHHLHNBC_04313 | 9e-136 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
JHHLHNBC_04314 | 0.0 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
JHHLHNBC_04315 | 1.7e-24 | |||||
JHHLHNBC_04318 | 9.3e-14 | |||||
JHHLHNBC_04319 | 5.8e-25 | |||||
JHHLHNBC_04321 | 7.9e-200 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
JHHLHNBC_04322 | 8.9e-223 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
JHHLHNBC_04323 | 2.3e-139 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
JHHLHNBC_04324 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
JHHLHNBC_04325 | 5.4e-61 | yrgI | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
JHHLHNBC_04326 | 8.9e-63 | |||||
JHHLHNBC_04327 | 9.7e-129 | S | SseB protein N-terminal domain | |||
JHHLHNBC_04328 | 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 | |
JHHLHNBC_04329 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
JHHLHNBC_04330 | 8.4e-93 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
JHHLHNBC_04331 | 2.7e-73 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
JHHLHNBC_04332 | 7.4e-138 | lacR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_04333 | 2.2e-116 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
JHHLHNBC_04334 | 6e-205 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
JHHLHNBC_04335 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
JHHLHNBC_04336 | 1.2e-34 | S | Plasmid maintenance system killer | |||
JHHLHNBC_04337 | 3.9e-51 | higA | K | Helix-turn-helix XRE-family like proteins | ||
JHHLHNBC_04338 | 1.3e-14 | |||||
JHHLHNBC_04339 | 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 | |
JHHLHNBC_04340 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
JHHLHNBC_04341 | 2.9e-263 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
JHHLHNBC_04342 | 1e-113 | ylbE | GM | NAD(P)H-binding | ||
JHHLHNBC_04343 | 3.7e-160 | yeaE | S | Aldo/keto reductase family | ||
JHHLHNBC_04344 | 2.1e-255 | yifK | E | Amino acid permease | ||
JHHLHNBC_04345 | 1.3e-283 | S | Protein of unknown function (DUF3800) | |||
JHHLHNBC_04346 | 0.0 | yjcE | P | Sodium proton antiporter | ||
JHHLHNBC_04347 | 2.2e-56 | S | Protein of unknown function (DUF3021) | |||
JHHLHNBC_04348 | 2.1e-68 | K | LytTr DNA-binding domain | |||
JHHLHNBC_04349 | 1.2e-147 | cylB | V | ABC-2 type transporter | ||
JHHLHNBC_04350 | 5.7e-158 | cylA | V | ABC transporter | ||
JHHLHNBC_04351 | 3.5e-135 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
JHHLHNBC_04352 | 1.6e-73 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
JHHLHNBC_04353 | 1.2e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
JHHLHNBC_04354 | 2e-121 | yvqF | S | Cell wall-active antibiotics response 4TMS YvqF | ||
JHHLHNBC_04355 | 3.5e-172 | vraS | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_04356 | 9e-78 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
JHHLHNBC_04357 | 1.9e-225 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
JHHLHNBC_04358 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
JHHLHNBC_04359 | 4.5e-58 | 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 | ||
JHHLHNBC_04360 | 2.7e-271 | L | Uncharacterised protein family (UPF0236) | |||
JHHLHNBC_04361 | 2.7e-42 | 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 | ||
JHHLHNBC_04362 | 9.9e-94 | rpiB | 2.1.1.222, 2.1.1.64, 5.3.1.26, 5.3.1.6 | G | Ribose/Galactose Isomerase | |
JHHLHNBC_04363 | 6.1e-73 | lacA | 5.3.1.26 | G | Ribose/Galactose Isomerase | |
JHHLHNBC_04364 | 1.9e-141 | lacR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_04365 | 3.8e-116 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
JHHLHNBC_04366 | 1.7e-15 | S | TPM domain | |||
JHHLHNBC_04367 | 1.1e-129 | yxaA | S | Sulfite exporter TauE/SafE | ||
JHHLHNBC_04368 | 2.7e-56 | ywjH | S | Protein of unknown function (DUF1634) | ||
JHHLHNBC_04370 | 2.2e-65 | |||||
JHHLHNBC_04371 | 5.5e-52 | |||||
JHHLHNBC_04372 | 6.4e-84 | fld | C | Flavodoxin | ||
JHHLHNBC_04373 | 3.4e-36 | |||||
JHHLHNBC_04374 | 6.7e-27 | |||||
JHHLHNBC_04375 | 1.2e-279 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
JHHLHNBC_04376 | 1.2e-238 | YSH1 | S | Metallo-beta-lactamase superfamily | ||
JHHLHNBC_04377 | 8.7e-50 | |||||
JHHLHNBC_04378 | 1.2e-115 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
JHHLHNBC_04379 | 1.1e-205 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
JHHLHNBC_04382 | 5.7e-255 | M | domain protein | |||
JHHLHNBC_04383 | 0.0 | M | TIGRFAM conserved repeat domain protein | |||
JHHLHNBC_04384 | 1.9e-189 | S | Bacterial protein of unknown function (DUF916) | |||
JHHLHNBC_04385 | 6.9e-179 | S | Bacterial protein of unknown function (DUF916) | |||
JHHLHNBC_04387 | 1.1e-161 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_04388 | 5.7e-107 | |||||
JHHLHNBC_04390 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
JHHLHNBC_04391 | 1.4e-145 | S | Alpha beta hydrolase | |||
JHHLHNBC_04392 | 5.1e-116 | yviA | S | Protein of unknown function (DUF421) | ||
JHHLHNBC_04393 | 9.1e-75 | S | Protein of unknown function (DUF3290) | |||
JHHLHNBC_04394 | 2.9e-223 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
JHHLHNBC_04395 | 6.3e-87 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
JHHLHNBC_04396 | 4.6e-103 | yjbF | S | SNARE associated Golgi protein | ||
JHHLHNBC_04397 | 8.7e-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 | |
JHHLHNBC_04398 | 4.9e-193 | 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 | |
JHHLHNBC_04399 | 2.1e-207 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
JHHLHNBC_04400 | 5.1e-89 | |||||
JHHLHNBC_04401 | 1.5e-116 | ydfK | S | Protein of unknown function (DUF554) | ||
JHHLHNBC_04402 | 5.6e-193 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
JHHLHNBC_04403 | 9.4e-58 | |||||
JHHLHNBC_04404 | 2.4e-47 | |||||
JHHLHNBC_04405 | 6.8e-207 | yueF | S | AI-2E family transporter | ||
JHHLHNBC_04406 | 8.6e-75 | S | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_04407 | 1.2e-96 | |||||
JHHLHNBC_04408 | 1.4e-104 | ygaC | J | Belongs to the UPF0374 family | ||
JHHLHNBC_04409 | 2.3e-201 | S | Calcineurin-like phosphoesterase | |||
JHHLHNBC_04410 | 6.7e-162 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
JHHLHNBC_04411 | 3.3e-175 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
JHHLHNBC_04412 | 1.8e-210 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
JHHLHNBC_04413 | 1.4e-159 | natA | S | ABC transporter | ||
JHHLHNBC_04414 | 1.7e-208 | ysdA | CP | ABC-2 family transporter protein | ||
JHHLHNBC_04415 | 4e-63 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
JHHLHNBC_04416 | 2.9e-162 | CcmA | V | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_04417 | 2.3e-108 | I | ABC-2 family transporter protein | |||
JHHLHNBC_04418 | 6.4e-199 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
JHHLHNBC_04419 | 3.7e-185 | tdcB | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
JHHLHNBC_04420 | 0.0 | S | OPT oligopeptide transporter protein | |||
JHHLHNBC_04421 | 3.1e-62 | S | Coenzyme PQQ synthesis protein D (PqqD) | |||
JHHLHNBC_04422 | 2.8e-271 | pipD | E | Dipeptidase | ||
JHHLHNBC_04423 | 2e-260 | gor | 1.8.1.7 | C | Glutathione reductase | |
JHHLHNBC_04424 | 2.9e-244 | lmrB | EGP | Major facilitator Superfamily | ||
JHHLHNBC_04425 | 2e-95 | yxaF | K | Transcriptional regulator | ||
JHHLHNBC_04426 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
JHHLHNBC_04427 | 3.2e-283 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
JHHLHNBC_04428 | 0.0 | bglP | G | phosphotransferase system | ||
JHHLHNBC_04429 | 6.3e-154 | licT | K | CAT RNA binding domain | ||
JHHLHNBC_04430 | 1.5e-289 | cydC | V | ABC transporter transmembrane region | ||
JHHLHNBC_04431 | 5.7e-308 | cydD | CO | ABC transporter transmembrane region | ||
JHHLHNBC_04432 | 2.7e-65 | ynhH | S | NusG domain II | ||
JHHLHNBC_04434 | 5.8e-86 | S | CRISPR-associated protein (Cas_Csn2) | |||
JHHLHNBC_04435 | 9.4e-44 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
JHHLHNBC_04436 | 2e-150 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
JHHLHNBC_04437 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
JHHLHNBC_04438 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
JHHLHNBC_04439 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
JHHLHNBC_04440 | 2.5e-181 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
JHHLHNBC_04441 | 1e-68 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
JHHLHNBC_04442 | 0.0 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
JHHLHNBC_04447 | 7.8e-160 | K | sequence-specific DNA binding | |||
JHHLHNBC_04448 | 1.4e-150 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_04449 | 1e-190 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_04450 | 1.8e-221 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04451 | 3.4e-99 | |||||
JHHLHNBC_04452 | 4.3e-289 | glnP | P | ABC transporter permease | ||
JHHLHNBC_04453 | 1.4e-133 | glnQ | E | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04454 | 1.7e-38 | |||||
JHHLHNBC_04455 | 1.3e-235 | G | Bacterial extracellular solute-binding protein | |||
JHHLHNBC_04456 | 2.6e-191 | 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 | |
JHHLHNBC_04457 | 3.5e-42 | 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 | ||
JHHLHNBC_04458 | 8.5e-63 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
JHHLHNBC_04459 | 3e-198 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
JHHLHNBC_04460 | 2.1e-146 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
JHHLHNBC_04461 | 1.4e-113 | cutC | P | Participates in the control of copper homeostasis | ||
JHHLHNBC_04462 | 3.4e-197 | 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 | |
JHHLHNBC_04464 | 3e-170 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_04465 | 1.2e-151 | 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 | |
JHHLHNBC_04466 | 1.2e-123 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
JHHLHNBC_04467 | 1.3e-105 | yjbK | S | CYTH | ||
JHHLHNBC_04468 | 4.3e-115 | yjbH | Q | Thioredoxin | ||
JHHLHNBC_04470 | 8.8e-206 | coiA | 3.6.4.12 | |||
JHHLHNBC_04471 | 1.1e-245 | XK27_08635 | S | UPF0210 protein | ||
JHHLHNBC_04472 | 1.8e-38 | gcvR | T | Belongs to the UPF0237 family | ||
JHHLHNBC_04473 | 4e-256 | cpdA | S | Calcineurin-like phosphoesterase | ||
JHHLHNBC_04474 | 1.9e-233 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
JHHLHNBC_04475 | 1.8e-86 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
JHHLHNBC_04476 | 6.3e-190 | 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 | |
JHHLHNBC_04477 | 3.5e-42 | 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 | ||
JHHLHNBC_04478 | 4.2e-62 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
JHHLHNBC_04479 | 8.6e-198 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
JHHLHNBC_04480 | 3.5e-146 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
JHHLHNBC_04481 | 4.4e-112 | cutC | P | Participates in the control of copper homeostasis | ||
JHHLHNBC_04482 | 1.7e-201 | 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 | |
JHHLHNBC_04483 | 3.3e-169 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_04484 | 1.4e-150 | 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 | |
JHHLHNBC_04485 | 2.3e-122 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
JHHLHNBC_04486 | 2.7e-103 | yjbK | S | CYTH | ||
JHHLHNBC_04487 | 5.6e-115 | yjbH | Q | Thioredoxin | ||
JHHLHNBC_04488 | 5.5e-208 | coiA | 3.6.4.12 | S | Competence protein | |
JHHLHNBC_04489 | 6.7e-243 | XK27_08635 | S | UPF0210 protein | ||
JHHLHNBC_04490 | 1.5e-37 | gcvR | T | Belongs to the UPF0237 family | ||
JHHLHNBC_04491 | 7.6e-223 | cpdA | S | Calcineurin-like phosphoesterase | ||
JHHLHNBC_04492 | 1.3e-226 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
JHHLHNBC_04493 | 5.8e-64 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
JHHLHNBC_04494 | 3.5e-175 | S | Bacterial protein of unknown function (DUF916) | |||
JHHLHNBC_04495 | 9.4e-110 | S | CAAX protease self-immunity | |||
JHHLHNBC_04496 | 2.6e-197 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
JHHLHNBC_04497 | 3.3e-141 | |||||
JHHLHNBC_04498 | 1.8e-34 | |||||
JHHLHNBC_04499 | 2.8e-157 | ytrB | V | ABC transporter | ||
JHHLHNBC_04500 | 1e-57 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
JHHLHNBC_04501 | 3.3e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
JHHLHNBC_04502 | 0.0 | bglB | 3.2.1.21 | GH3 | G | hydrolase, family 3 |
JHHLHNBC_04504 | 2.8e-174 | oppB | P | ABC transporter permease | ||
JHHLHNBC_04505 | 8.2e-136 | oppC | EP | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_04506 | 4.8e-174 | holB | 2.7.7.7 | L | DNA polymerase III | |
JHHLHNBC_04507 | 3.5e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
JHHLHNBC_04508 | 1e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
JHHLHNBC_04509 | 1.9e-37 | S | Protein of unknown function (DUF2508) | |||
JHHLHNBC_04510 | 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 | ||
JHHLHNBC_04511 | 2.2e-32 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
JHHLHNBC_04512 | 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 | |
JHHLHNBC_04513 | 3.8e-170 | L | hmm pf00665 | |||
JHHLHNBC_04514 | 5.2e-111 | L | Helix-turn-helix domain | |||
JHHLHNBC_04515 | 3.1e-98 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
JHHLHNBC_04516 | 5.8e-34 | |||||
JHHLHNBC_04517 | 2.4e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
JHHLHNBC_04518 | 4.9e-218 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
JHHLHNBC_04519 | 5.5e-158 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_04520 | 1.3e-156 | I | alpha/beta hydrolase fold | |||
JHHLHNBC_04521 | 1.6e-57 | |||||
JHHLHNBC_04522 | 2.9e-69 | |||||
JHHLHNBC_04523 | 4.5e-152 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
JHHLHNBC_04524 | 9.4e-124 | citR | K | FCD | ||
JHHLHNBC_04525 | 2.2e-265 | oadA | 2.1.3.1, 4.1.1.3, 6.4.1.1, 6.4.1.7 | C | Conserved carboxylase domain | |
JHHLHNBC_04526 | 3.1e-98 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
JHHLHNBC_04527 | 7.8e-288 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
JHHLHNBC_04528 | 2.3e-151 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
JHHLHNBC_04529 | 1.7e-48 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
JHHLHNBC_04530 | 3.2e-181 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
JHHLHNBC_04532 | 6.7e-196 | oadB | 4.1.1.3 | C | Na+-transporting oxaloacetate decarboxylase beta subunit | |
JHHLHNBC_04533 | 3.5e-38 | gcdC | 2.3.1.12 | I | Biotin-requiring enzyme | |
JHHLHNBC_04534 | 4.1e-53 | |||||
JHHLHNBC_04535 | 4.8e-241 | citM | C | Citrate transporter | ||
JHHLHNBC_04536 | 1.7e-41 | |||||
JHHLHNBC_04537 | 4.5e-100 | kptA | J | Removes the 2'-phosphate from RNA via an intermediate in which the phosphate is ADP-ribosylated by NAD followed by a presumed transesterification to release the RNA and generate ADP- ribose 1''-2''-cyclic phosphate (APPR P). May function as an ADP- ribosylase | ||
JHHLHNBC_04538 | 1.3e-87 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_04539 | 4e-59 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_04540 | 1.3e-140 | ORF00048 | ||||
JHHLHNBC_04541 | 1.2e-132 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
JHHLHNBC_04542 | 1.1e-164 | ecsA_1 | S | ABC transporter | ||
JHHLHNBC_04543 | 1.5e-286 | M | Exporter of polyketide antibiotics | |||
JHHLHNBC_04544 | 7e-110 | K | Transcriptional regulator | |||
JHHLHNBC_04545 | 4.4e-115 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04546 | 4.1e-128 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04547 | 1.1e-125 | S | membrane transporter protein | |||
JHHLHNBC_04548 | 4.9e-185 | K | Helix-turn-helix domain | |||
JHHLHNBC_04549 | 4.6e-157 | S | Alpha beta hydrolase | |||
JHHLHNBC_04550 | 2.4e-52 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
JHHLHNBC_04551 | 4.2e-127 | skfE | V | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_04552 | 3.7e-14 | |||||
JHHLHNBC_04553 | 1.5e-158 | oppF | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
JHHLHNBC_04554 | 2.6e-197 | oppD | P | Oligopeptide/dipeptide transporter, C-terminal region | ||
JHHLHNBC_04555 | 2.6e-49 | |||||
JHHLHNBC_04556 | 1.2e-172 | amiD | P | N-terminal TM domain of oligopeptide transport permease C | ||
JHHLHNBC_04557 | 8e-166 | oppB | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_04558 | 9.3e-311 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
JHHLHNBC_04559 | 2.3e-38 | |||||
JHHLHNBC_04560 | 9e-282 | V | ABC transporter transmembrane region | |||
JHHLHNBC_04561 | 1.1e-281 | V | ABC transporter transmembrane region | |||
JHHLHNBC_04562 | 5.7e-65 | S | Iron-sulphur cluster biosynthesis | |||
JHHLHNBC_04564 | 1.4e-137 | 2.7.1.39 | S | Phosphotransferase enzyme family | ||
JHHLHNBC_04565 | 4.2e-117 | zmp3 | O | Zinc-dependent metalloprotease | ||
JHHLHNBC_04566 | 4.9e-222 | |||||
JHHLHNBC_04567 | 8e-73 | V | ABC transporter | |||
JHHLHNBC_04568 | 7.4e-95 | K | Helix-turn-helix domain | |||
JHHLHNBC_04569 | 6.9e-217 | lytN | 3.5.1.104 | M | LysM domain | |
JHHLHNBC_04570 | 1.3e-33 | lciIC | K | Helix-turn-helix XRE-family like proteins | ||
JHHLHNBC_04571 | 5.1e-235 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
JHHLHNBC_04572 | 2.1e-100 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
JHHLHNBC_04573 | 9.5e-86 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
JHHLHNBC_04574 | 3.1e-57 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
JHHLHNBC_04575 | 6.8e-145 | folP | 2.5.1.15, 2.7.6.3 | H | dihydropteroate synthase | |
JHHLHNBC_04576 | 2.2e-66 | yjdB | S | Domain of unknown function (DUF4767) | ||
JHHLHNBC_04577 | 5.5e-81 | S | Fic/DOC family | |||
JHHLHNBC_04578 | 1.2e-32 | S | Cysteine-rich secretory protein family | |||
JHHLHNBC_04580 | 3.2e-23 | K | Cro/C1-type HTH DNA-binding domain | |||
JHHLHNBC_04581 | 8.2e-50 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
JHHLHNBC_04582 | 2.3e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
JHHLHNBC_04583 | 4.1e-245 | Z012_01130 | S | Fic/DOC family | ||
JHHLHNBC_04584 | 1.1e-163 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
JHHLHNBC_04585 | 4.4e-157 | I | alpha/beta hydrolase fold | |||
JHHLHNBC_04586 | 3.9e-49 | |||||
JHHLHNBC_04587 | 1.7e-69 | |||||
JHHLHNBC_04588 | 1.7e-159 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
JHHLHNBC_04589 | 7.2e-124 | citR | K | FCD | ||
JHHLHNBC_04590 | 6.9e-267 | oadA | 2.1.3.1, 4.1.1.3, 6.4.1.1, 6.4.1.7 | C | Conserved carboxylase domain | |
JHHLHNBC_04591 | 5.2e-101 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
JHHLHNBC_04592 | 1.3e-287 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
JHHLHNBC_04593 | 6.9e-156 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
JHHLHNBC_04594 | 2.2e-48 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
JHHLHNBC_04595 | 2.6e-183 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
JHHLHNBC_04597 | 1e-196 | oadB | 4.1.1.3 | C | Na+-transporting oxaloacetate decarboxylase beta subunit | |
JHHLHNBC_04598 | 1.6e-26 | gcdC | 2.3.1.12 | I | Biotin-requiring enzyme | |
JHHLHNBC_04599 | 2e-230 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
JHHLHNBC_04600 | 3e-195 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
JHHLHNBC_04601 | 1.1e-168 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
JHHLHNBC_04602 | 2.6e-219 | patA | 2.6.1.1 | E | Aminotransferase | |
JHHLHNBC_04603 | 2.8e-38 | |||||
JHHLHNBC_04604 | 4.5e-20 | |||||
JHHLHNBC_04605 | 0.0 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase concanavalin-like domain | ||
JHHLHNBC_04607 | 1.2e-285 | G | MFS/sugar transport protein | |||
JHHLHNBC_04608 | 6.7e-78 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
JHHLHNBC_04609 | 8.8e-38 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
JHHLHNBC_04610 | 9.7e-18 | |||||
JHHLHNBC_04611 | 5.8e-169 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_04612 | 1.6e-261 | M | domain protein | |||
JHHLHNBC_04613 | 2.3e-116 | GM | NmrA-like family | |||
JHHLHNBC_04614 | 3.7e-168 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_04615 | 1e-196 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
JHHLHNBC_04616 | 3.3e-175 | proV | E | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04617 | 1.6e-252 | gshR | 1.8.1.7 | C | Glutathione reductase | |
JHHLHNBC_04618 | 4.3e-141 | fruR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_04619 | 7.4e-169 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
JHHLHNBC_04620 | 0.0 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
JHHLHNBC_04621 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
JHHLHNBC_04622 | 3.1e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_04623 | 1e-260 | glnPH2 | P | ABC transporter permease | ||
JHHLHNBC_04624 | 4.5e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
JHHLHNBC_04625 | 7e-295 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
JHHLHNBC_04626 | 2.4e-56 | S | Domain of unknown function (DUF1827) | |||
JHHLHNBC_04627 | 1.7e-125 | K | Mga helix-turn-helix domain | |||
JHHLHNBC_04628 | 2e-55 | |||||
JHHLHNBC_04629 | 2.3e-281 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
JHHLHNBC_04630 | 1.6e-68 | yqeY | S | YqeY-like protein | ||
JHHLHNBC_04631 | 1.5e-100 | tnpB | L | Putative transposase DNA-binding domain | ||
JHHLHNBC_04632 | 1e-122 | S | Alpha/beta hydrolase family | |||
JHHLHNBC_04633 | 1.3e-260 | arpJ | P | ABC transporter permease | ||
JHHLHNBC_04634 | 2e-233 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
JHHLHNBC_04635 | 1.5e-202 | rny | S | Endoribonuclease that initiates mRNA decay | ||
JHHLHNBC_04636 | 2.1e-117 | yvyE | 3.4.13.9 | S | YigZ family | |
JHHLHNBC_04637 | 1.4e-234 | comFA | L | Helicase C-terminal domain protein | ||
JHHLHNBC_04638 | 1.8e-89 | comFC | S | Competence protein | ||
JHHLHNBC_04639 | 3.9e-47 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
JHHLHNBC_04640 | 3e-164 | yvgN | C | Aldo keto reductase | ||
JHHLHNBC_04641 | 8.7e-142 | iolR | K | DeoR C terminal sensor domain | ||
JHHLHNBC_04642 | 1.1e-267 | iolT | EGP | Major facilitator Superfamily | ||
JHHLHNBC_04643 | 3e-273 | iolA | 1.2.1.18, 1.2.1.27 | C | Belongs to the aldehyde dehydrogenase family | |
JHHLHNBC_04644 | 7.6e-157 | iolB | 5.3.1.30 | G | Involved in the isomerization of 5-deoxy-glucuronate (5DG) to 5-dehydro-2-deoxy-D-gluconate (DKG or 2-deoxy-5-keto-D- gluconate) | |
JHHLHNBC_04645 | 3.8e-179 | iolC | 2.7.1.92 | H | Catalyzes the phosphorylation of 5-dehydro-2-deoxy-D- gluconate (2-deoxy-5-keto-D-gluconate or DKG) to 6-phospho-5- dehydro-2-deoxy-D-gluconate (DKGP) | |
JHHLHNBC_04646 | 1.3e-238 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
JHHLHNBC_04647 | 1.2e-219 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_04648 | 2.5e-121 | K | response regulator | |||
JHHLHNBC_04649 | 1.5e-118 | |||||
JHHLHNBC_04650 | 7.9e-227 | uvrA2 | L | ABC transporter | ||
JHHLHNBC_04651 | 3.5e-188 | ampC | V | Beta-lactamase | ||
JHHLHNBC_04652 | 3.6e-165 | 1.13.11.2 | S | glyoxalase | ||
JHHLHNBC_04653 | 8.6e-139 | S | NADPH-dependent FMN reductase | |||
JHHLHNBC_04654 | 0.0 | yfiC | V | ABC transporter | ||
JHHLHNBC_04655 | 0.0 | ycfI | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_04656 | 2.2e-122 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04657 | 5.9e-121 | G | Phosphoglycerate mutase family | |||
JHHLHNBC_04658 | 4.1e-08 | |||||
JHHLHNBC_04659 | 1.2e-79 | K | Putative DNA-binding domain | |||
JHHLHNBC_04660 | 1.5e-09 | |||||
JHHLHNBC_04661 | 2.8e-63 | S | Phage derived protein Gp49-like (DUF891) | |||
JHHLHNBC_04662 | 5.2e-41 | K | Helix-turn-helix domain | |||
JHHLHNBC_04663 | 1.4e-18 | V | Type II restriction enzyme, methylase subunits | |||
JHHLHNBC_04664 | 1.1e-124 | tnp | L | DDE domain | ||
JHHLHNBC_04665 | 1.7e-84 | dps | P | Belongs to the Dps family | ||
JHHLHNBC_04666 | 9.1e-133 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_04667 | 3.4e-164 | V | ABC-type multidrug transport system, permease component | |||
JHHLHNBC_04668 | 4.1e-116 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04669 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
JHHLHNBC_04670 | 4.6e-32 | copZ | P | Heavy-metal-associated domain | ||
JHHLHNBC_04671 | 1.2e-97 | dps | P | Belongs to the Dps family | ||
JHHLHNBC_04672 | 9.5e-167 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
JHHLHNBC_04673 | 7.1e-167 | XK27_07135 | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
JHHLHNBC_04674 | 3.7e-180 | 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 | |
JHHLHNBC_04675 | 7.1e-136 | cad | S | FMN_bind | ||
JHHLHNBC_04676 | 9.4e-138 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
JHHLHNBC_04677 | 2.4e-96 | 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 | |||
JHHLHNBC_04678 | 1.4e-45 | fer | C | 4Fe-4S single cluster domain of Ferredoxin I | ||
JHHLHNBC_04679 | 9.7e-183 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
JHHLHNBC_04680 | 5e-265 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
JHHLHNBC_04681 | 2.7e-56 | M | Lysin motif | |||
JHHLHNBC_04682 | 2.6e-115 | 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 | |
JHHLHNBC_04683 | 4.7e-94 | M1-874 | K | Domain of unknown function (DUF1836) | ||
JHHLHNBC_04684 | 7.3e-302 | cpdB | 3.1.3.6, 3.1.4.16 | F | 5'-nucleotidase, C-terminal domain | |
JHHLHNBC_04685 | 1.3e-127 | |||||
JHHLHNBC_04686 | 6.5e-22 | S | Protein of unknown function (DUF2929) | |||
JHHLHNBC_04687 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
JHHLHNBC_04689 | 9.4e-211 | mutY | L | A G-specific adenine glycosylase | ||
JHHLHNBC_04690 | 1e-150 | cytC6 | I | alpha/beta hydrolase fold | ||
JHHLHNBC_04691 | 8.8e-117 | yrkL | S | Flavodoxin-like fold | ||
JHHLHNBC_04693 | 9.1e-87 | S | Short repeat of unknown function (DUF308) | |||
JHHLHNBC_04694 | 5.9e-37 | relB | L | RelB antitoxin | ||
JHHLHNBC_04695 | 2.3e-113 | S | Psort location Cytoplasmic, score | |||
JHHLHNBC_04696 | 4.6e-154 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
JHHLHNBC_04697 | 4e-198 | |||||
JHHLHNBC_04698 | 4.6e-08 | |||||
JHHLHNBC_04699 | 3e-116 | ywnB | S | NmrA-like family | ||
JHHLHNBC_04700 | 7.4e-10 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_04701 | 2.2e-09 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_04702 | 1.1e-128 | 4.1.2.14 | S | KDGP aldolase | ||
JHHLHNBC_04703 | 1.3e-191 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
JHHLHNBC_04704 | 8.1e-210 | dho | 3.5.2.3 | S | Amidohydrolase family | |
JHHLHNBC_04705 | 1.4e-116 | S | Domain of unknown function (DUF4310) | |||
JHHLHNBC_04706 | 3.7e-137 | S | Domain of unknown function (DUF4311) | |||
JHHLHNBC_04707 | 9e-57 | S | Domain of unknown function (DUF4312) | |||
JHHLHNBC_04708 | 1.2e-61 | S | Glycine-rich SFCGS | |||
JHHLHNBC_04709 | 3.1e-54 | S | PRD domain | |||
JHHLHNBC_04710 | 0.0 | K | Mga helix-turn-helix domain | |||
JHHLHNBC_04711 | 3.2e-113 | tal | 2.2.1.2 | H | Pfam:Transaldolase | |
JHHLHNBC_04712 | 1.6e-53 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
JHHLHNBC_04713 | 5.6e-187 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
JHHLHNBC_04714 | 3.5e-97 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
JHHLHNBC_04715 | 2.4e-52 | gutM | K | Glucitol operon activator protein (GutM) | ||
JHHLHNBC_04716 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
JHHLHNBC_04717 | 1.1e-136 | IQ | NAD dependent epimerase/dehydratase family | |||
JHHLHNBC_04718 | 1.7e-148 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
JHHLHNBC_04719 | 0.0 | O | Belongs to the peptidase S8 family | |||
JHHLHNBC_04720 | 5.2e-38 | |||||
JHHLHNBC_04722 | 5.3e-140 | metC1 | 4.4.1.8 | E | cystathionine | |
JHHLHNBC_04723 | 1.2e-85 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
JHHLHNBC_04724 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
JHHLHNBC_04725 | 6e-194 | gutB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
JHHLHNBC_04726 | 3.2e-123 | gatD | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
JHHLHNBC_04727 | 3e-221 | gatC | G | PTS system sugar-specific permease component | ||
JHHLHNBC_04728 | 1e-34 | 2.7.1.200 | G | protein-N(PI)-phosphohistidine-sugar phosphotransferase activity | ||
JHHLHNBC_04729 | 1.1e-56 | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_04730 | 4.4e-114 | K | DeoR C terminal sensor domain | |||
JHHLHNBC_04731 | 4.5e-126 | tnp | L | DDE domain | ||
JHHLHNBC_04733 | 8.4e-88 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_04734 | 4.9e-92 | S | Protein of unknown function (DUF1211) | |||
JHHLHNBC_04735 | 4.4e-83 | ycaQ | S | Winged helix DNA-binding domain | ||
JHHLHNBC_04736 | 1.9e-38 | S | Protein of unknown function (DUF1093) | |||
JHHLHNBC_04737 | 7.3e-99 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
JHHLHNBC_04739 | 2.6e-08 | S | Protein of unknown function (DUF3923) | |||
JHHLHNBC_04740 | 0.0 | sca1 | G | Belongs to the glycosyl hydrolase 31 family | ||
JHHLHNBC_04742 | 8.8e-22 | M | MucBP domain | |||
JHHLHNBC_04743 | 5.9e-237 | 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 | |
JHHLHNBC_04744 | 1.8e-101 | pncA | Q | Isochorismatase family | ||
JHHLHNBC_04745 | 2.1e-118 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
JHHLHNBC_04746 | 9.9e-120 | E | IrrE N-terminal-like domain | |||
JHHLHNBC_04748 | 5.9e-126 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
JHHLHNBC_04749 | 1e-56 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
JHHLHNBC_04750 | 2.4e-227 | ugpB | G | Bacterial extracellular solute-binding protein | ||
JHHLHNBC_04751 | 4.6e-146 | ugpE | G | ABC transporter permease | ||
JHHLHNBC_04752 | 8.4e-160 | ugpA | P | ABC-type sugar transport systems, permease components | ||
JHHLHNBC_04753 | 2.5e-203 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
JHHLHNBC_04754 | 2.6e-180 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_04755 | 7.6e-146 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
JHHLHNBC_04756 | 6.9e-184 | blaA6 | V | Beta-lactamase | ||
JHHLHNBC_04757 | 1.3e-141 | 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 | |
JHHLHNBC_04758 | 1.2e-158 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
JHHLHNBC_04759 | 2.4e-81 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_04760 | 6.4e-151 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_04761 | 1.1e-129 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_04762 | 1.6e-216 | S | endonuclease exonuclease phosphatase family protein | |||
JHHLHNBC_04763 | 2e-169 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
JHHLHNBC_04764 | 1.5e-138 | Q | Methyltransferase | |||
JHHLHNBC_04765 | 3.7e-51 | sugE | U | Multidrug resistance protein | ||
JHHLHNBC_04768 | 4.7e-48 | |||||
JHHLHNBC_04769 | 1.6e-121 | S | -acetyltransferase | |||
JHHLHNBC_04770 | 1.8e-81 | MA20_25245 | K | FR47-like protein | ||
JHHLHNBC_04771 | 1.5e-92 | hisB | 2.7.7.71, 3.1.3.15, 3.1.3.82, 3.1.3.83, 4.2.1.19, 5.3.1.28, 6.3.2.10 | GT9 | E | HAD-hyrolase-like |
JHHLHNBC_04772 | 5.1e-131 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
JHHLHNBC_04773 | 3.2e-121 | |||||
JHHLHNBC_04774 | 4.7e-24 | |||||
JHHLHNBC_04775 | 2.8e-34 | DJ | ParE toxin of type II toxin-antitoxin system, parDE | |||
JHHLHNBC_04777 | 2.4e-155 | G | Carbohydrate esterase, sialic acid-specific acetylesterase | |||
JHHLHNBC_04778 | 2.3e-75 | 6.3.3.2 | S | ASCH | ||
JHHLHNBC_04779 | 1.5e-199 | Z012_01130 | S | Fic/DOC family | ||
JHHLHNBC_04780 | 2.3e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
JHHLHNBC_04781 | 6.3e-183 | ybiR | P | Citrate transporter | ||
JHHLHNBC_04782 | 4.7e-177 | K | helix_turn _helix lactose operon repressor | |||
JHHLHNBC_04783 | 2.5e-138 | kguE | 2.7.1.45 | G | Xylose isomerase domain protein TIM barrel | |
JHHLHNBC_04784 | 6.4e-38 | |||||
JHHLHNBC_04785 | 5.4e-226 | C | C4-dicarboxylate transmembrane transporter activity | |||
JHHLHNBC_04786 | 2.5e-183 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
JHHLHNBC_04787 | 2.4e-102 | hxlA | 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase HUMPS family | |
JHHLHNBC_04788 | 5.3e-90 | hxlB | 4.1.2.14, 4.1.2.43, 4.1.3.42, 5.3.1.27 | M | sugar phosphate isomerase involved in capsule formation | |
JHHLHNBC_04789 | 1.8e-89 | |||||
JHHLHNBC_04790 | 8e-17 | K | sequence-specific DNA binding | |||
JHHLHNBC_04791 | 1.4e-248 | E | Peptidase dimerisation domain | |||
JHHLHNBC_04792 | 1.6e-299 | E | ABC transporter, substratebinding protein | |||
JHHLHNBC_04794 | 6.8e-28 | |||||
JHHLHNBC_04795 | 8.6e-292 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 | |
JHHLHNBC_04796 | 2.1e-304 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
JHHLHNBC_04797 | 3.5e-174 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
JHHLHNBC_04798 | 8.1e-131 | K | response regulator | |||
JHHLHNBC_04799 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
JHHLHNBC_04800 | 1.3e-260 | yycH | S | YycH protein | ||
JHHLHNBC_04801 | 1.1e-141 | yycI | S | YycH protein | ||
JHHLHNBC_04802 | 2.7e-154 | vicX | 3.1.26.11 | S | domain protein | |
JHHLHNBC_04803 | 2e-10 | |||||
JHHLHNBC_04804 | 6.3e-201 | htrA | 3.4.21.107 | O | serine protease | |
JHHLHNBC_04805 | 5.9e-70 | S | Iron-sulphur cluster biosynthesis | |||
JHHLHNBC_04806 | 2.7e-76 | hsp3 | O | Hsp20/alpha crystallin family | ||
JHHLHNBC_04807 | 0.0 | cadA | P | P-type ATPase | ||
JHHLHNBC_04808 | 6.6e-133 | |||||
JHHLHNBC_04809 | 1.3e-173 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
JHHLHNBC_04810 | 2.2e-102 | dhaL | 2.7.1.121 | S | Dak2 | |
JHHLHNBC_04811 | 6.2e-58 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
JHHLHNBC_04812 | 7.5e-103 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04813 | 9.5e-14 | |||||
JHHLHNBC_04814 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
JHHLHNBC_04815 | 2.5e-178 | |||||
JHHLHNBC_04816 | 4.2e-197 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
JHHLHNBC_04817 | 2.9e-154 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
JHHLHNBC_04819 | 0.0 | S | X-Pro dipeptidyl-peptidase C-terminal non-catalytic domain | |||
JHHLHNBC_04820 | 1.6e-191 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
JHHLHNBC_04821 | 1.5e-281 | oppA | E | ABC transporter, substratebinding protein | ||
JHHLHNBC_04822 | 1.5e-180 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
JHHLHNBC_04823 | 7.2e-104 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
JHHLHNBC_04825 | 2e-116 | S | Fic/DOC family | |||
JHHLHNBC_04826 | 3.3e-287 | yfiB | V | ABC transporter transmembrane region | ||
JHHLHNBC_04827 | 0.0 | md2 | V | ABC transporter | ||
JHHLHNBC_04828 | 9.7e-241 | V | ABC-type multidrug transport system, ATPase and permease components | |||
JHHLHNBC_04829 | 1.5e-141 | K | Transcriptional activator, Rgg GadR MutR family | |||
JHHLHNBC_04830 | 7.4e-23 | |||||
JHHLHNBC_04831 | 6.2e-78 | 5.3.1.27 | M | arabinose-5-phosphate isomerase activity | ||
JHHLHNBC_04832 | 4.1e-124 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
JHHLHNBC_04833 | 3.3e-56 | kdsD | 5.3.1.13 | M | SIS domain | |
JHHLHNBC_04834 | 1.3e-64 | S | Uncharacterised protein family UPF0047 | |||
JHHLHNBC_04835 | 8.4e-34 | 2.7.1.200 | G | protein-N(PI)-phosphohistidine-sugar phosphotransferase activity | ||
JHHLHNBC_04836 | 2.9e-185 | G | PTS system sugar-specific permease component | |||
JHHLHNBC_04837 | 4e-75 | 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_04838 | 2.1e-306 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
JHHLHNBC_04839 | 2.1e-39 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
JHHLHNBC_04840 | 8.3e-105 | lacI3 | K | helix_turn _helix lactose operon repressor | ||
JHHLHNBC_04841 | 5.3e-221 | malL | 3.2.1.10 | GH13 | G | Alpha-amylase domain |
JHHLHNBC_04842 | 9.9e-36 | 2.7.1.191 | G | PTS system fructose IIA component | ||
JHHLHNBC_04843 | 1.2e-125 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_04844 | 4.7e-103 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_04845 | 3.3e-59 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_04846 | 1.5e-152 | S | hydrolase | |||
JHHLHNBC_04847 | 1e-270 | npr | 1.11.1.1 | C | NADH oxidase | |
JHHLHNBC_04848 | 1.9e-121 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
JHHLHNBC_04849 | 2.7e-186 | hrtB | V | ABC transporter permease | ||
JHHLHNBC_04850 | 1e-87 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
JHHLHNBC_04851 | 6.2e-145 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
JHHLHNBC_04852 | 1.3e-17 | S | YvrJ protein family | |||
JHHLHNBC_04854 | 2.5e-08 | pnb | C | nitroreductase | ||
JHHLHNBC_04855 | 4.6e-79 | |||||
JHHLHNBC_04856 | 9.8e-172 | EGP | COG COG0477 Permeases of the major facilitator superfamily | |||
JHHLHNBC_04857 | 4.2e-130 | rihA | F | Inosine-uridine preferring nucleoside hydrolase | ||
JHHLHNBC_04858 | 5.4e-280 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
JHHLHNBC_04859 | 3.2e-157 | rapL | 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | |
JHHLHNBC_04860 | 7.3e-142 | S | Sulfite exporter TauE/SafE | |||
JHHLHNBC_04861 | 2.1e-93 | 6.3.4.4 | S | Zeta toxin | ||
JHHLHNBC_04862 | 2.3e-156 | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | ||
JHHLHNBC_04863 | 1.4e-53 | |||||
JHHLHNBC_04864 | 2.8e-206 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
JHHLHNBC_04865 | 2.2e-48 | ptxB | 2.7.1.194, 2.7.1.200, 2.7.1.204 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_04866 | 2.5e-180 | GKT | transcriptional antiterminator | |||
JHHLHNBC_04867 | 2.2e-19 | yjdB | S | Domain of unknown function (DUF4767) | ||
JHHLHNBC_04868 | 3.5e-35 | XK27_08465 | 2.7.1.191 | G | PTS system fructose IIA component | |
JHHLHNBC_04869 | 4.3e-115 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_04870 | 1.1e-96 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_04871 | 2.1e-58 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_04872 | 2.5e-71 | K | UTRA | |||
JHHLHNBC_04873 | 1.4e-149 | glmS2 | G | Catalyzes the conversion of a range of fructosamine 6- phosphates to glucose 6-phosphate and a free amino acid | ||
JHHLHNBC_04874 | 5.1e-255 | frdC | 1.3.5.4 | C | HI0933-like protein | |
JHHLHNBC_04875 | 7.1e-30 | |||||
JHHLHNBC_04876 | 2.2e-102 | |||||
JHHLHNBC_04877 | 2.3e-72 | K | helix_turn_helix multiple antibiotic resistance protein | |||
JHHLHNBC_04878 | 2.4e-240 | ydiC1 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_04879 | 3.3e-175 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
JHHLHNBC_04880 | 7.4e-139 | mtsC | U | ABC 3 transport family | ||
JHHLHNBC_04881 | 2.3e-116 | mntB | 3.6.3.35 | P | ABC transporter | |
JHHLHNBC_04882 | 1.7e-148 | malK | P | ATPases associated with a variety of cellular activities | ||
JHHLHNBC_04883 | 7.5e-166 | malG | P | ABC-type sugar transport systems, permease components | ||
JHHLHNBC_04884 | 9.5e-283 | mga | K | Mga helix-turn-helix domain | ||
JHHLHNBC_04885 | 0.0 | sprD | D | Domain of Unknown Function (DUF1542) | ||
JHHLHNBC_04886 | 4.2e-308 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
JHHLHNBC_04887 | 2.2e-68 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
JHHLHNBC_04888 | 2.1e-135 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
JHHLHNBC_04889 | 1.7e-218 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
JHHLHNBC_04890 | 6.6e-125 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
JHHLHNBC_04891 | 3.9e-281 | 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 | |
JHHLHNBC_04892 | 3.1e-223 | V | Beta-lactamase | |||
JHHLHNBC_04893 | 6.3e-151 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
JHHLHNBC_04894 | 1.9e-209 | V | Beta-lactamase | |||
JHHLHNBC_04895 | 7.3e-150 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
JHHLHNBC_04896 | 8.4e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
JHHLHNBC_04897 | 1.2e-106 | yktB | S | Belongs to the UPF0637 family | ||
JHHLHNBC_04898 | 4.6e-73 | yueI | S | Protein of unknown function (DUF1694) | ||
JHHLHNBC_04899 | 0.0 | 6.3.2.2, 6.3.2.4 | M | Mur ligase middle domain protein | ||
JHHLHNBC_04900 | 1.4e-171 | pfoS | S | Phosphotransferase system, EIIC | ||
JHHLHNBC_04901 | 6.2e-51 | S | MazG-like family | |||
JHHLHNBC_04902 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
JHHLHNBC_04904 | 3.2e-161 | degV | S | EDD domain protein, DegV family | ||
JHHLHNBC_04905 | 1.5e-100 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
JHHLHNBC_04906 | 3.9e-209 | hisC | 2.6.1.9 | E | Cys/Met metabolism PLP-dependent enzyme | |
JHHLHNBC_04907 | 3.1e-217 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
JHHLHNBC_04908 | 6.1e-99 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_04909 | 1e-109 | |||||
JHHLHNBC_04910 | 7.2e-159 | S | ABC-type transport system involved in multi-copper enzyme maturation permease component | |||
JHHLHNBC_04911 | 8.6e-117 | |||||
JHHLHNBC_04912 | 3.5e-111 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04913 | 7.5e-298 | norB | EGP | Major Facilitator | ||
JHHLHNBC_04915 | 6e-33 | |||||
JHHLHNBC_04916 | 1.9e-80 | fld | C | Flavodoxin | ||
JHHLHNBC_04917 | 9.6e-178 | yihY | S | Belongs to the UPF0761 family | ||
JHHLHNBC_04918 | 4e-259 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
JHHLHNBC_04919 | 2.7e-111 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04920 | 1.3e-237 | pepS | E | Thermophilic metalloprotease (M29) | ||
JHHLHNBC_04921 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
JHHLHNBC_04922 | 3.9e-240 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
JHHLHNBC_04923 | 1.9e-115 | S | Haloacid dehalogenase-like hydrolase | |||
JHHLHNBC_04924 | 4.3e-118 | radC | L | DNA repair protein | ||
JHHLHNBC_04925 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_04926 | 8.9e-220 | S | GcrA cell cycle regulator | |||
JHHLHNBC_04927 | 9.2e-55 | S | HNH endonuclease | |||
JHHLHNBC_04928 | 1.9e-50 | |||||
JHHLHNBC_04931 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
JHHLHNBC_04932 | 1e-162 | S | Tetratricopeptide repeat | |||
JHHLHNBC_04933 | 5.5e-206 | 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 | ||
JHHLHNBC_04934 | 1.3e-39 | 3.4.21.88 | K | Helix-turn-helix | ||
JHHLHNBC_04935 | 3.9e-09 | K | Helix-turn-helix XRE-family like proteins | |||
JHHLHNBC_04937 | 5.7e-98 | S | DNA binding | |||
JHHLHNBC_04938 | 4.2e-121 | S | sequence-specific DNA binding | |||
JHHLHNBC_04939 | 3.6e-38 | S | sequence-specific DNA binding | |||
JHHLHNBC_04940 | 4.3e-79 | K | Phage regulatory protein | |||
JHHLHNBC_04941 | 2e-127 | S | Sulfite exporter TauE/SafE | |||
JHHLHNBC_04942 | 1.2e-249 | 3.5.4.28, 3.5.4.31 | F | Amidohydrolase family | ||
JHHLHNBC_04943 | 4.3e-69 | S | An automated process has identified a potential problem with this gene model | |||
JHHLHNBC_04944 | 2.2e-64 | S | Protein of unknown function (DUF3100) | |||
JHHLHNBC_04945 | 9.5e-53 | S | Protein of unknown function (DUF3100) | |||
JHHLHNBC_04946 | 2.2e-114 | S | YheO-like PAS domain | |||
JHHLHNBC_04947 | 4.3e-134 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
JHHLHNBC_04948 | 6e-64 | 3.5.99.10 | J | Endoribonuclease L-PSP | ||
JHHLHNBC_04949 | 1.8e-230 | steT_1 | E | amino acid | ||
JHHLHNBC_04950 | 1.3e-139 | puuD | S | peptidase C26 | ||
JHHLHNBC_04951 | 1.5e-110 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_04952 | 3.3e-172 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
JHHLHNBC_04953 | 1e-105 | opuCB | E | ABC transporter permease | ||
JHHLHNBC_04954 | 1.2e-222 | opuCA | 2.7.7.7 | E | ABC transporter, ATP-binding protein | |
JHHLHNBC_04956 | 6.1e-24 | ypbD | S | CAAX protease self-immunity | ||
JHHLHNBC_04957 | 3.7e-27 | |||||
JHHLHNBC_04958 | 6.5e-62 | plnD | K | LytTr DNA-binding domain | ||
JHHLHNBC_04959 | 3e-70 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
JHHLHNBC_04960 | 4.7e-10 | S | CAAX amino terminal protease family | |||
JHHLHNBC_04961 | 8.2e-191 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |||
JHHLHNBC_04962 | 0.0 | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | ||
JHHLHNBC_04963 | 4.7e-32 | copZ | P | Heavy-metal-associated domain | ||
JHHLHNBC_04964 | 1.4e-96 | dps | P | Belongs to the Dps family | ||
JHHLHNBC_04965 | 1.4e-116 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
JHHLHNBC_04966 | 6.2e-130 | S | CAAX protease self-immunity | |||
JHHLHNBC_04967 | 2.2e-221 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
JHHLHNBC_04968 | 1.9e-47 | S | Domain of unknown function (DUF4260) | |||
JHHLHNBC_04969 | 9.5e-309 | norB | EGP | Major Facilitator | ||
JHHLHNBC_04970 | 1.4e-104 | K | Bacterial regulatory proteins, tetR family | |||
JHHLHNBC_04971 | 1.1e-55 | |||||
JHHLHNBC_04972 | 1e-84 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
JHHLHNBC_04973 | 7.9e-211 | nusA | K | Participates in both transcription termination and antitermination | ||
JHHLHNBC_04974 | 1.5e-46 | ylxR | K | Protein of unknown function (DUF448) | ||
JHHLHNBC_04975 | 5.4e-44 | ylxQ | J | ribosomal protein | ||
JHHLHNBC_04976 | 1.2e-111 | |||||
JHHLHNBC_04977 | 0.0 | VPA1266 | 3.1.11.5 | L | Helix-hairpin-helix containing domain | |
JHHLHNBC_04978 | 5.3e-133 | XK27_05520 | S | Uncharacterized protein conserved in bacteria (DUF2087) | ||
JHHLHNBC_04979 | 2.4e-133 | S | Belongs to the UPF0246 family | |||
JHHLHNBC_04980 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
JHHLHNBC_04981 | 6e-210 | |||||
JHHLHNBC_04982 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
JHHLHNBC_04983 | 2.2e-168 | |||||
JHHLHNBC_04984 | 3.7e-249 | 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 | |
JHHLHNBC_04985 | 4.1e-178 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
JHHLHNBC_04986 | 1e-240 | ytoI | K | DRTGG domain | ||
JHHLHNBC_04987 | 7e-206 | 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 | |
JHHLHNBC_04988 | 9.5e-175 | oppB | P | ABC transporter permease | ||
JHHLHNBC_04989 | 2e-142 | oppC | EP | Binding-protein-dependent transport system inner membrane component | ||
JHHLHNBC_04990 | 7.1e-77 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
JHHLHNBC_04991 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
JHHLHNBC_04992 | 3.8e-162 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
JHHLHNBC_04993 | 2.9e-190 | 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 | ||
JHHLHNBC_04994 | 6.6e-292 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
JHHLHNBC_04995 | 3.6e-76 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
JHHLHNBC_04996 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
JHHLHNBC_04997 | 3.7e-54 | |||||
JHHLHNBC_04998 | 3e-57 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
JHHLHNBC_04999 | 1.1e-169 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
JHHLHNBC_05000 | 1.5e-297 | tagE | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
JHHLHNBC_05001 | 5.9e-299 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
JHHLHNBC_05002 | 2e-12 | N | PPE family | |||
JHHLHNBC_05004 | 4.4e-108 | speG | J | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_05005 | 4.9e-54 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
JHHLHNBC_05006 | 1.3e-51 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
JHHLHNBC_05007 | 6.9e-130 | K | UbiC transcription regulator-associated domain protein | |||
JHHLHNBC_05008 | 2e-239 | celB | 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 | |
JHHLHNBC_05009 | 1.2e-73 | S | Domain of unknown function (DUF3284) | |||
JHHLHNBC_05010 | 2.2e-215 | S | Bacterial protein of unknown function (DUF871) | |||
JHHLHNBC_05011 | 3.8e-162 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
JHHLHNBC_05012 | 1.5e-54 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
JHHLHNBC_05013 | 1.6e-26 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
JHHLHNBC_05014 | 3.9e-125 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
JHHLHNBC_05015 | 4.4e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
JHHLHNBC_05016 | 2e-233 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
JHHLHNBC_05017 | 4.1e-192 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
JHHLHNBC_05018 | 1.8e-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 | |
JHHLHNBC_05019 | 4.8e-191 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
JHHLHNBC_05020 | 2.7e-43 | |||||
JHHLHNBC_05021 | 5.6e-106 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
JHHLHNBC_05022 | 0.0 | |||||
JHHLHNBC_05024 | 2.2e-124 | yqcC | S | WxL domain surface cell wall-binding | ||
JHHLHNBC_05025 | 1.1e-184 | ynjC | S | Cell surface protein | ||
JHHLHNBC_05026 | 2.6e-272 | L | Mga helix-turn-helix domain | |||
JHHLHNBC_05027 | 6.7e-176 | yhaI | S | Protein of unknown function (DUF805) | ||
JHHLHNBC_05028 | 9.4e-58 | |||||
JHHLHNBC_05029 | 1.4e-253 | rarA | L | recombination factor protein RarA | ||
JHHLHNBC_05030 | 1.7e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
JHHLHNBC_05031 | 9.4e-239 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
JHHLHNBC_05032 | 9.6e-180 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
JHHLHNBC_05033 | 0.0 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
JHHLHNBC_05034 | 1.5e-158 | pfkB | 2.7.1.11, 2.7.1.144, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
JHHLHNBC_05035 | 5.6e-85 | asnB | 6.3.5.4 | E | Asparagine synthase | |
JHHLHNBC_05036 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
JHHLHNBC_05037 | 2.3e-259 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
JHHLHNBC_05038 | 6.6e-153 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
JHHLHNBC_05039 | 5.9e-143 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
JHHLHNBC_05040 | 1e-234 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
JHHLHNBC_05041 | 7.7e-301 | scrB | 3.2.1.26 | GH32 | G | invertase |
JHHLHNBC_05042 | 7.3e-178 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
JHHLHNBC_05043 | 0.0 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
JHHLHNBC_05044 | 1.1e-83 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
JHHLHNBC_05045 | 4.9e-259 | 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 | ||
JHHLHNBC_05046 | 7.7e-217 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
JHHLHNBC_05047 | 9.4e-228 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
JHHLHNBC_05048 | 1.7e-117 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
JHHLHNBC_05049 | 4.8e-182 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
JHHLHNBC_05050 | 1.1e-181 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
JHHLHNBC_05051 | 2.9e-96 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
JHHLHNBC_05052 | 3.1e-144 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
JHHLHNBC_05053 | 1.8e-167 | murB | 1.3.1.98 | M | Cell wall formation | |
JHHLHNBC_05054 | 0.0 | yjcE | P | Sodium proton antiporter | ||
JHHLHNBC_05055 | 2.9e-96 | puuR | K | Cupin domain | ||
JHHLHNBC_05056 | 1.2e-205 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
JHHLHNBC_05057 | 2.9e-148 | potB | P | ABC transporter permease | ||
JHHLHNBC_05058 | 8.9e-145 | potC | P | ABC transporter permease | ||
JHHLHNBC_05059 | 1e-206 | potD | P | ABC transporter | ||
JHHLHNBC_05061 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
JHHLHNBC_05062 | 3e-108 | K | Transcriptional regulator | |||
JHHLHNBC_05063 | 1.9e-174 | V | ABC transporter | |||
JHHLHNBC_05064 | 1e-128 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
JHHLHNBC_05065 | 1e-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 | |
JHHLHNBC_05066 | 9.2e-166 | ybbR | S | YbbR-like protein | ||
JHHLHNBC_05067 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
JHHLHNBC_05068 | 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 | |
JHHLHNBC_05069 | 0.0 | pepF2 | E | Oligopeptidase F | ||
JHHLHNBC_05070 | 3.3e-10 | |||||
JHHLHNBC_05071 | 6.5e-151 | 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 | ||
JHHLHNBC_05072 | 3.6e-149 | 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 | ||
JHHLHNBC_05073 | 2.7e-111 | tdk | 2.7.1.21 | F | thymidine kinase | |
JHHLHNBC_05074 | 5.1e-53 | trxA | O | Belongs to the thioredoxin family | ||
JHHLHNBC_05075 | 4.5e-296 | 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 | |
JHHLHNBC_05076 | 1.2e-238 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
JHHLHNBC_05077 | 2.4e-37 | 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 | |
JHHLHNBC_05078 | 7.8e-263 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
JHHLHNBC_05079 | 1.6e-79 | ctsR | K | Belongs to the CtsR family | ||
JHHLHNBC_05080 | 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 | ||
JHHLHNBC_05083 | 1.4e-68 | V | Best Blastp hit gi 7514214 pir G75157 'abc transporter, ATP-binding protein, puta tive PAB2069 - Pyrococcus abyssi (strain Orsay)' gi 5457852 emb CAB49342.1 '(AJ248284) ABC transporter, ATP-binding protein, puta tive Pyrococcus abyssi ', score 77, E-value 3.00E-13 | |||
JHHLHNBC_05084 | 6e-163 | V | ABC transporter | |||
JHHLHNBC_05085 | 3.7e-234 | alfA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
JHHLHNBC_05086 | 1e-56 | |||||
JHHLHNBC_05087 | 0.0 | pckG | 4.1.1.32, 4.1.1.49 | C | Phosphoenolpyruvate carboxykinase | |
JHHLHNBC_05088 | 1.6e-24 | S | Virus attachment protein p12 family | |||
JHHLHNBC_05089 | 9.4e-118 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
JHHLHNBC_05090 | 2.1e-73 | ssb_2 | L | Single-strand binding protein family | ||
JHHLHNBC_05092 | 3e-15 | |||||
JHHLHNBC_05094 | 4.7e-08 | ssb_2 | L | Single-strand binding protein family | ||
JHHLHNBC_05095 | 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 | |
JHHLHNBC_05096 | 5.1e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
JHHLHNBC_05097 | 2.1e-191 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
JHHLHNBC_05098 | 4.5e-157 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
JHHLHNBC_05099 | 4.7e-174 | 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 | ||
JHHLHNBC_05100 | 1.4e-45 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
JHHLHNBC_05101 | 4e-27 | |||||
JHHLHNBC_05102 | 3.7e-258 | yvlB | S | Putative adhesin | ||
JHHLHNBC_05103 | 2.1e-194 | ylbL | T | Belongs to the peptidase S16 family | ||
JHHLHNBC_05104 | 7.4e-118 | comEA | L | Competence protein ComEA | ||
JHHLHNBC_05105 | 1.6e-210 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
JHHLHNBC_05106 | 6.2e-135 | S | E1-E2 ATPase | |||
JHHLHNBC_05107 | 1.2e-100 | 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 | |
JHHLHNBC_05108 | 3.9e-26 | |||||
JHHLHNBC_05109 | 1.4e-72 | |||||
JHHLHNBC_05110 | 1.4e-242 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
JHHLHNBC_05111 | 2.9e-243 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
JHHLHNBC_05112 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
JHHLHNBC_05113 | 4.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
JHHLHNBC_05114 | 1.5e-88 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
JHHLHNBC_05115 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
JHHLHNBC_05116 | 1.9e-65 | |||||
JHHLHNBC_05117 | 1.3e-128 | S | SseB protein N-terminal domain | |||
JHHLHNBC_05118 | 3.4e-137 | cobB | K | Sir2 family | ||
JHHLHNBC_05119 | 1.8e-235 | EGP | Major Facilitator Superfamily | |||
JHHLHNBC_05120 | 0.0 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
JHHLHNBC_05121 | 2.3e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
JHHLHNBC_05122 | 2e-194 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
JHHLHNBC_05123 | 2.7e-51 | |||||
JHHLHNBC_05124 | 1.3e-90 | S | MucBP domain | |||
JHHLHNBC_05125 | 2.7e-117 | ywnB | S | NAD(P)H-binding | ||
JHHLHNBC_05126 | 2e-149 | manN | G | system, mannose fructose sorbose family IID component | ||
JHHLHNBC_05127 | 2.6e-64 | manO | S | Domain of unknown function (DUF956) | ||
JHHLHNBC_05128 | 1.4e-129 | iolS | C | Aldo keto reductase | ||
JHHLHNBC_05129 | 5e-210 | yeaN | P | Transporter, major facilitator family protein | ||
JHHLHNBC_05130 | 3.7e-247 | ydiC1 | EGP | Major facilitator Superfamily | ||
JHHLHNBC_05131 | 1.7e-93 | ycaC | Q | Isochorismatase family | ||
JHHLHNBC_05132 | 4.1e-234 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
JHHLHNBC_05134 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
JHHLHNBC_05135 | 8.1e-44 | 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 | ||
JHHLHNBC_05136 | 1.6e-140 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
JHHLHNBC_05137 | 1.7e-139 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
JHHLHNBC_05138 | 4e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
JHHLHNBC_05139 | 2.2e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
JHHLHNBC_05140 | 2e-155 | 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 | ||
JHHLHNBC_05141 | 3.9e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
JHHLHNBC_05142 | 6.3e-196 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
JHHLHNBC_05143 | 0.0 | comEC | S | Competence protein ComEC | ||
JHHLHNBC_05144 | 5.8e-107 | comEA | L | Competence protein ComEA | ||
JHHLHNBC_05145 | 2.8e-199 | ylbL | T | Belongs to the peptidase S16 family | ||
JHHLHNBC_05146 | 5.6e-86 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
JHHLHNBC_05147 | 2.9e-99 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
JHHLHNBC_05148 | 4.6e-55 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
JHHLHNBC_05149 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
JHHLHNBC_05150 | 8.6e-207 | ftsW | D | Belongs to the SEDS family | ||
JHHLHNBC_05151 | 0.0 | typA | T | GTP-binding protein TypA | ||
JHHLHNBC_05152 | 5.5e-209 | yubA | S | AI-2E family transporter | ||
JHHLHNBC_05153 | 3.4e-80 | |||||
JHHLHNBC_05154 | 6.3e-47 | |||||
JHHLHNBC_05155 | 3.5e-191 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
JHHLHNBC_05156 | 2.1e-48 | |||||
JHHLHNBC_05157 | 1.1e-52 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
JHHLHNBC_05158 | 8.1e-54 | K | Transcriptional regulator PadR-like family | |||
JHHLHNBC_05159 | 1.4e-165 | |||||
JHHLHNBC_05161 | 1.7e-28 | |||||
JHHLHNBC_05162 | 4.4e-83 | usp6 | T | universal stress protein | ||
JHHLHNBC_05163 | 3.7e-157 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
JHHLHNBC_05164 | 1.9e-178 | S | Protein of unknown function (DUF2785) | |||
JHHLHNBC_05165 | 2.9e-66 | yueI | S | Protein of unknown function (DUF1694) | ||
JHHLHNBC_05166 | 1.8e-26 | |||||
JHHLHNBC_05167 | 5.6e-280 | sufB | O | assembly protein SufB | ||
JHHLHNBC_05168 | 1.3e-78 | nifU | C | SUF system FeS assembly protein, NifU family | ||
JHHLHNBC_05169 | 3.1e-223 | csdA | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
JHHLHNBC_05170 | 1.5e-189 | sufD | O | FeS assembly protein SufD | ||
JHHLHNBC_05171 | 1.3e-142 | sufC | O | FeS assembly ATPase SufC | ||
JHHLHNBC_05172 | 4.4e-105 | metI | P | ABC transporter permease | ||
JHHLHNBC_05173 | 4.1e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
JHHLHNBC_05174 | 1.7e-148 | P | Belongs to the nlpA lipoprotein family | |||
JHHLHNBC_05175 | 1.3e-140 | P | Belongs to the nlpA lipoprotein family | |||
JHHLHNBC_05176 | 5.1e-212 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
JHHLHNBC_05177 | 1.9e-49 | gcvH | E | glycine cleavage | ||
JHHLHNBC_05178 | 2.4e-223 | rodA | D | Belongs to the SEDS family | ||
JHHLHNBC_05179 | 9.9e-35 | S | Protein of unknown function (DUF2969) | |||
JHHLHNBC_05180 | 4.1e-55 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
JHHLHNBC_05181 | 1.4e-25 | S | DNA-directed RNA polymerase subunit beta | |||
JHHLHNBC_05182 | 1e-179 | mbl | D | Cell shape determining protein MreB Mrl | ||
JHHLHNBC_05183 | 2e-236 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
JHHLHNBC_05184 | 1e-171 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
JHHLHNBC_05185 | 4.6e-38 | |||||
JHHLHNBC_05186 | 4.9e-87 | |||||
JHHLHNBC_05187 | 2.7e-24 | |||||
JHHLHNBC_05188 | 1.5e-161 | yicL | EG | EamA-like transporter family | ||
JHHLHNBC_05189 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
JHHLHNBC_05190 | 1.2e-68 | |||||
JHHLHNBC_05191 | 1.1e-30 | K | Transcriptional | |||
JHHLHNBC_05192 | 0.0 | V | ABC transporter | |||
JHHLHNBC_05193 | 0.0 | V | ABC transporter | |||
JHHLHNBC_05194 | 5.6e-169 | 2.7.13.3 | T | GHKL domain | ||
JHHLHNBC_05195 | 7.8e-126 | T | LytTr DNA-binding domain | |||
JHHLHNBC_05196 | 1.1e-172 | yqhA | G | Aldose 1-epimerase | ||
JHHLHNBC_05197 | 6.2e-38 | S | YopX protein | |||
JHHLHNBC_05199 | 2.9e-21 | |||||
JHHLHNBC_05201 | 1.8e-32 | S | Protein of unknown function (DUF1642) | |||
JHHLHNBC_05202 | 3.7e-127 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
JHHLHNBC_05204 | 4.6e-56 | S | Protein of unknown function (DUF1064) | |||
JHHLHNBC_05205 | 1.2e-148 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
JHHLHNBC_05206 | 4.5e-120 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
JHHLHNBC_05208 | 7.2e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
JHHLHNBC_05209 | 1.4e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
JHHLHNBC_05211 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
JHHLHNBC_05212 | 9.1e-253 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
JHHLHNBC_05213 | 6.7e-260 | K | Mga helix-turn-helix domain | |||
JHHLHNBC_05214 | 0.0 | N | domain, Protein | |||
JHHLHNBC_05215 | 3.8e-137 | S | WxL domain surface cell wall-binding | |||
JHHLHNBC_05217 | 7e-187 | S | Cell surface protein | |||
JHHLHNBC_05218 | 7.4e-73 | T | Sh3 type 3 domain protein | |||
JHHLHNBC_05219 | 7.4e-34 | |||||
JHHLHNBC_05220 | 2.5e-32 | |||||
JHHLHNBC_05221 | 5.4e-08 | |||||
JHHLHNBC_05223 | 8.8e-09 | yhjA | S | CsbD-like | ||
JHHLHNBC_05224 | 4.8e-194 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
JHHLHNBC_05225 | 7.2e-46 | |||||
JHHLHNBC_05226 | 5.3e-201 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
JHHLHNBC_05227 | 1.9e-121 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
JHHLHNBC_05228 | 2e-92 | ccpN | K | Domain in cystathionine beta-synthase and other proteins. | ||
JHHLHNBC_05229 | 0.0 | ppdK | 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
JHHLHNBC_05230 | 0.0 | kup | P | Transport of potassium into the cell | ||
JHHLHNBC_05231 | 1.9e-166 | V | ATPases associated with a variety of cellular activities | |||
JHHLHNBC_05232 | 2.1e-211 | S | ABC-2 family transporter protein | |||
JHHLHNBC_05233 | 4.5e-197 | |||||
JHHLHNBC_05234 | 3.2e-261 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
JHHLHNBC_05235 | 8.8e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
JHHLHNBC_05236 | 4.2e-49 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
JHHLHNBC_05237 | 3.2e-261 | nox | 1.6.3.4 | C | NADH oxidase | |
JHHLHNBC_05238 | 1.7e-116 | |||||
JHHLHNBC_05239 | 5.5e-225 | mtnE | 2.6.1.83 | E | Aminotransferase | |
JHHLHNBC_05240 | 3.7e-145 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
JHHLHNBC_05241 | 5.4e-150 | M | NLPA lipoprotein | |||
JHHLHNBC_05244 | 1.2e-85 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
JHHLHNBC_05245 | 1.3e-134 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
JHHLHNBC_05246 | 1.6e-57 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
JHHLHNBC_05247 | 6e-52 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
JHHLHNBC_05248 | 5.2e-209 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
JHHLHNBC_05249 | 1.2e-149 | Q | Fumarylacetoacetate (FAA) hydrolase family | |||
JHHLHNBC_05250 | 8.9e-113 | nfnB | 1.5.1.34 | C | Nitroreductase family | |
JHHLHNBC_05251 | 6.9e-71 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_05252 | 5.4e-68 | msi198 | K | Acetyltransferase (GNAT) domain | ||
JHHLHNBC_05253 | 1.5e-222 | EGP | Transmembrane secretion effector | |||
JHHLHNBC_05254 | 4.8e-128 | T | Transcriptional regulatory protein, C terminal | |||
JHHLHNBC_05255 | 2.5e-175 | T | Histidine kinase-like ATPases | |||
JHHLHNBC_05256 | 2.6e-135 | XK27_05695 | V | ABC transporter, ATP-binding protein | ||
JHHLHNBC_05257 | 0.0 | ysaB | V | FtsX-like permease family | ||
JHHLHNBC_05258 | 9.5e-211 | xerS | L | Belongs to the 'phage' integrase family | ||
JHHLHNBC_05259 | 3.6e-171 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
JHHLHNBC_05260 | 1.8e-181 | K | LysR substrate binding domain | |||
JHHLHNBC_05261 | 4.3e-171 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
JHHLHNBC_05262 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
JHHLHNBC_05263 | 2.8e-171 | corA | P | CorA-like Mg2+ transporter protein | ||
JHHLHNBC_05264 | 1.5e-132 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
JHHLHNBC_05265 | 4.5e-108 | pncA | Q | Isochorismatase family | ||
JHHLHNBC_05266 | 1.1e-270 | 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 | |
JHHLHNBC_05267 | 3.2e-132 | glpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
JHHLHNBC_05268 | 9.3e-71 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
JHHLHNBC_05269 | 2.9e-241 | ugpB | G | Bacterial extracellular solute-binding protein | ||
JHHLHNBC_05270 | 2.2e-148 | ugpE | G | ABC transporter permease | ||
JHHLHNBC_05271 | 6.6e-165 | ugpA | P | ABC-type sugar transport systems, permease components | ||
JHHLHNBC_05272 | 2.5e-211 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
JHHLHNBC_05273 | 3.2e-226 | EGP | Major facilitator Superfamily | |||
JHHLHNBC_05274 | 8.6e-150 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
JHHLHNBC_05275 | 1.7e-198 | blaA6 | V | Beta-lactamase | ||
JHHLHNBC_05276 | 7.4e-150 | 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 | |
JHHLHNBC_05277 | 6.7e-165 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
JHHLHNBC_05278 | 1.5e-80 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
JHHLHNBC_05279 | 4.9e-151 | G | PTS system mannose/fructose/sorbose family IID component | |||
JHHLHNBC_05280 | 3.3e-131 | G | PTS system sorbose-specific iic component | |||
JHHLHNBC_05282 | 2.4e-203 | S | endonuclease exonuclease phosphatase family protein | |||
JHHLHNBC_05283 | 2e-174 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
JHHLHNBC_05284 | 4.5e-160 | 1.1.1.346 | S | reductase | ||
JHHLHNBC_05285 | 1.3e-75 | adhR | K | helix_turn_helix, mercury resistance | ||
JHHLHNBC_05286 | 6.1e-145 | Q | Methyltransferase | |||
JHHLHNBC_05287 | 1e-173 | draG | 3.2.2.24 | O | ADP-ribosylglycohydrolase | |
JHHLHNBC_05288 | 1.7e-51 | sugE | U | Multidrug resistance protein | ||
JHHLHNBC_05291 | 3.1e-61 | |||||
JHHLHNBC_05292 | 1.2e-36 | |||||
JHHLHNBC_05293 | 2.4e-110 | S | alpha beta | |||
JHHLHNBC_05294 | 2.8e-90 | MA20_25245 | K | FR47-like protein | ||
JHHLHNBC_05295 | 5.9e-132 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
JHHLHNBC_05296 | 3.8e-84 | K | Acetyltransferase (GNAT) domain | |||
JHHLHNBC_05297 | 3.1e-124 | |||||
JHHLHNBC_05298 | 4.7e-68 | 6.3.3.2 | S | ASCH | ||
JHHLHNBC_05299 | 5.2e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
JHHLHNBC_05300 | 4.1e-198 | ybiR | P | Citrate transporter | ||
JHHLHNBC_05301 | 9.6e-102 | |||||
JHHLHNBC_05302 | 7e-253 | E | Peptidase dimerisation domain | |||
JHHLHNBC_05303 | 8.1e-73 | E | ABC transporter, substratebinding protein | |||
JHHLHNBC_05304 | 8.8e-215 | E | ABC transporter, substratebinding protein | |||
JHHLHNBC_05305 | 2.7e-16 | UW | Tetratricopeptide repeat | |||
JHHLHNBC_05306 | 7.9e-274 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
JHHLHNBC_05307 | 0.0 | bglH | G | phosphotransferase system | ||
JHHLHNBC_05308 | 9.1e-150 | licT2 | K | CAT RNA binding domain | ||
JHHLHNBC_05309 | 0.0 | S | Bacterial membrane protein YfhO | |||
JHHLHNBC_05310 | 1.8e-309 | S | Psort location CytoplasmicMembrane, score | |||
JHHLHNBC_05311 | 3.3e-172 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
JHHLHNBC_05312 | 2.1e-77 | |||||
JHHLHNBC_05313 | 7.1e-170 | yqjA | S | Putative aromatic acid exporter C-terminal domain | ||
JHHLHNBC_05314 | 1.6e-31 | cspC | K | Cold shock protein | ||
JHHLHNBC_05315 | 6.6e-84 | yvbK | 3.1.3.25 | K | GNAT family | |
JHHLHNBC_05316 | 1.6e-109 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
JHHLHNBC_05317 | 4.2e-101 | 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 | |
JHHLHNBC_05318 | 4e-240 | pbuX | F | xanthine permease | ||
JHHLHNBC_05319 | 4.1e-206 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
JHHLHNBC_05320 | 1.4e-242 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
JHHLHNBC_05321 | 2.4e-101 | |||||
JHHLHNBC_05322 | 5.9e-132 | |||||
JHHLHNBC_05323 | 6.9e-113 | pacL | 3.6.3.8 | P | P-type ATPase | |
JHHLHNBC_05324 | 8.1e-128 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
JHHLHNBC_05325 | 1.2e-135 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
JHHLHNBC_05326 | 2.3e-270 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
JHHLHNBC_05327 | 2.4e-256 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
JHHLHNBC_05328 | 2.1e-54 | |||||
JHHLHNBC_05329 | 4.9e-188 | yibE | S | overlaps another CDS with the same product name | ||
JHHLHNBC_05330 | 5.9e-116 | yibF | S | overlaps another CDS with the same product name | ||
JHHLHNBC_05331 | 1.8e-115 | S | Calcineurin-like phosphoesterase | |||
JHHLHNBC_05332 | 1.7e-265 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
JHHLHNBC_05333 | 2.6e-109 | yutD | S | Protein of unknown function (DUF1027) | ||
JHHLHNBC_05334 | 2.2e-145 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
JHHLHNBC_05335 | 6.1e-114 | S | Protein of unknown function (DUF1461) | |||
JHHLHNBC_05336 | 2.3e-116 | dedA | S | SNARE-like domain protein | ||
JHHLHNBC_05337 | 1.5e-86 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
JHHLHNBC_05338 | 3.3e-68 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
JHHLHNBC_05339 | 3.6e-168 | ykcA | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
JHHLHNBC_05340 | 7.3e-191 | mhqA | 3.4.21.26 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
JHHLHNBC_05341 | 1.8e-121 | mhqD | S | Dienelactone hydrolase family | ||
JHHLHNBC_05342 | 7.6e-180 | 3.5.1.10 | C | Alcohol dehydrogenase GroES-like domain | ||
JHHLHNBC_05343 | 7.7e-100 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
JHHLHNBC_05344 | 2.2e-35 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
JHHLHNBC_05345 | 2.5e-302 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
JHHLHNBC_05348 | 1e-187 | |||||
JHHLHNBC_05349 | 6e-17 | |||||
JHHLHNBC_05350 | 4e-53 | L | Transposase IS66 family | |||
JHHLHNBC_05351 | 3.2e-55 | |||||
JHHLHNBC_05352 | 8.1e-151 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
JHHLHNBC_05353 | 2.8e-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 | ||
JHHLHNBC_05354 | 9.5e-65 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
JHHLHNBC_05355 | 5.1e-66 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
JHHLHNBC_05356 | 1e-81 | 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 | |
JHHLHNBC_05357 | 5.7e-175 | phoH | T | phosphate starvation-inducible protein PhoH | ||
JHHLHNBC_05358 | 1.8e-67 | yqeY | S | YqeY-like protein |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)