ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
BNJPHLCL_00001 | 1.1e-59 | yuzD | S | protein conserved in bacteria | ||
BNJPHLCL_00002 | 2.2e-63 | erpA | S | Belongs to the HesB IscA family | ||
BNJPHLCL_00003 | 2.2e-75 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
BNJPHLCL_00004 | 4.1e-73 | yneN | CO | Thioredoxin-like | ||
BNJPHLCL_00006 | 6.7e-87 | pksA | K | Transcriptional regulator | ||
BNJPHLCL_00007 | 1.3e-96 | ymcC | S | Membrane | ||
BNJPHLCL_00010 | 9.3e-55 | |||||
BNJPHLCL_00011 | 5.6e-42 | |||||
BNJPHLCL_00012 | 2.6e-129 | V | ABC transporter | |||
BNJPHLCL_00013 | 1.3e-122 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNJPHLCL_00014 | 2.7e-250 | arlS | 2.7.13.3 | T | Histidine kinase | |
BNJPHLCL_00015 | 5.2e-38 | gcvR | T | Belongs to the UPF0237 family | ||
BNJPHLCL_00016 | 4.8e-249 | XK27_08635 | S | UPF0210 protein | ||
BNJPHLCL_00017 | 3.1e-38 | K | transcriptional | |||
BNJPHLCL_00018 | 1.9e-119 | L | Mu transposase, C-terminal | |||
BNJPHLCL_00020 | 4.2e-294 | mqo | 1.1.5.4 | S | malate quinone oxidoreductase | |
BNJPHLCL_00021 | 6.6e-31 | papP | E | amino acid ABC transporter | ||
BNJPHLCL_00026 | 1.7e-07 | |||||
BNJPHLCL_00027 | 1.5e-07 | |||||
BNJPHLCL_00031 | 6.3e-131 | L | Phage integrase, N-terminal SAM-like domain | |||
BNJPHLCL_00032 | 2e-45 | S | CRISPR-associated protein | |||
BNJPHLCL_00033 | 3.7e-249 | 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 | ||
BNJPHLCL_00034 | 3.9e-289 | bglA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BNJPHLCL_00035 | 5.5e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
BNJPHLCL_00036 | 1e-216 | ybbR | S | protein conserved in bacteria | ||
BNJPHLCL_00037 | 4.7e-146 | 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 | |
BNJPHLCL_00039 | 2.5e-56 | S | Heat induced stress protein YflT | |||
BNJPHLCL_00040 | 4.4e-134 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
BNJPHLCL_00041 | 1.9e-34 | S | Family of unknown function (DUF5327) | |||
BNJPHLCL_00042 | 1.1e-57 | ywdK | S | small membrane protein | ||
BNJPHLCL_00043 | 2.2e-81 | gerQ | S | Essential for the localization of CwlJ in the spore coat and for spore germination triggered by calcium and dipicolinic acid (DPA). Its assembly into the spore coat is dependent on the coat morphogenetic proteins CotE and SpoIVA | ||
BNJPHLCL_00046 | 1e-61 | V | DNA restriction-modification system | |||
BNJPHLCL_00047 | 3.1e-128 | V | AAA domain (dynein-related subfamily) | |||
BNJPHLCL_00055 | 1.7e-07 | |||||
BNJPHLCL_00056 | 8.7e-08 | |||||
BNJPHLCL_00060 | 1.6e-08 | |||||
BNJPHLCL_00063 | 1.1e-198 | adhC | 1.1.1.1 | C | Zinc-binding dehydrogenase | |
BNJPHLCL_00064 | 1.7e-190 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | |||
BNJPHLCL_00066 | 9.9e-101 | ycnI | S | Domain of unkown function (DUF1775) | ||
BNJPHLCL_00067 | 3.4e-289 | ycnJ | P | protein, homolog of Cu resistance protein CopC | ||
BNJPHLCL_00070 | 4.3e-49 | |||||
BNJPHLCL_00071 | 3e-13 | |||||
BNJPHLCL_00075 | 3.2e-118 | |||||
BNJPHLCL_00076 | 6.1e-233 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
BNJPHLCL_00077 | 2.7e-74 | cueR | K | transcriptional | ||
BNJPHLCL_00078 | 1.7e-249 | corC1 | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
BNJPHLCL_00080 | 3.4e-214 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_00081 | 6.7e-44 | 2.7.1.202 | K | transcriptional regulator, MtlR | ||
BNJPHLCL_00082 | 8e-255 | gph | G | MFS/sugar transport protein | ||
BNJPHLCL_00083 | 4.4e-114 | K | helix_turn_helix, arabinose operon control protein | |||
BNJPHLCL_00084 | 6.9e-74 | G | Glycosyl hydrolases family 39 | |||
BNJPHLCL_00085 | 1.5e-166 | ydjE | EGP | Major facilitator superfamily | ||
BNJPHLCL_00087 | 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 | |
BNJPHLCL_00088 | 1.7e-67 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
BNJPHLCL_00089 | 3.6e-48 | ykvR | S | Protein of unknown function (DUF3219) | ||
BNJPHLCL_00090 | 3.7e-174 | yceB | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
BNJPHLCL_00091 | 6.7e-58 | V | CAAX protease self-immunity | |||
BNJPHLCL_00092 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
BNJPHLCL_00093 | 0.0 | yyaL | O | COG1331 Highly conserved protein containing a thioredoxin domain | ||
BNJPHLCL_00094 | 1.8e-221 | ymfD | EGP | Major facilitator Superfamily | ||
BNJPHLCL_00098 | 1.8e-240 | P | Voltage gated chloride channel | |||
BNJPHLCL_00099 | 9.4e-49 | P | Rhodanese domain protein | |||
BNJPHLCL_00100 | 2.8e-36 | yhjE | S | protein conserved in bacteria | ||
BNJPHLCL_00101 | 3e-142 | yokF | 3.1.31.1 | L | RNA catabolic process | |
BNJPHLCL_00102 | 4e-71 | 2.7.1.199 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
BNJPHLCL_00103 | 3e-140 | |||||
BNJPHLCL_00104 | 2.9e-207 | |||||
BNJPHLCL_00105 | 1.9e-59 | asp | S | protein conserved in bacteria | ||
BNJPHLCL_00106 | 3e-301 | yloV | S | kinase related to dihydroxyacetone kinase | ||
BNJPHLCL_00107 | 1.3e-119 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
BNJPHLCL_00108 | 2.6e-155 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
BNJPHLCL_00109 | 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) | |
BNJPHLCL_00110 | 8.8e-99 | fapR | 5.3.1.23 | Q | Transcriptional factor involved in regulation of membrane lipid biosynthesis by repressing genes involved in fatty acid and phospholipid metabolism | |
BNJPHLCL_00111 | 2.5e-178 | 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 | |
BNJPHLCL_00112 | 4.2e-159 | fabD | 2.3.1.39 | I | malonyl CoA-acyl carrier protein transacylase | |
BNJPHLCL_00113 | 2.1e-129 | IQ | reductase | |||
BNJPHLCL_00114 | 3.7e-32 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BNJPHLCL_00115 | 1.5e-132 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
BNJPHLCL_00116 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
BNJPHLCL_00117 | 1.3e-179 | 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) | ||
BNJPHLCL_00118 | 2.9e-51 | 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 | ||
BNJPHLCL_00119 | 8.7e-243 | 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 | |
BNJPHLCL_00120 | 1.7e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
BNJPHLCL_00121 | 5.5e-36 | ylqC | S | Belongs to the UPF0109 family | ||
BNJPHLCL_00122 | 7.1e-60 | ylqD | S | YlqD protein | ||
BNJPHLCL_00123 | 1.2e-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 | ||
BNJPHLCL_00124 | 2e-140 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
BNJPHLCL_00125 | 2.4e-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 | ||
BNJPHLCL_00126 | 1.2e-102 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
BNJPHLCL_00127 | 4.7e-154 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
BNJPHLCL_00128 | 1.7e-129 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BNJPHLCL_00129 | 2.8e-227 | CP_1081 | D | nuclear chromosome segregation | ||
BNJPHLCL_00130 | 3.6e-45 | ylqH | S | homolog of the cytoplasmic domain of flagellar protein FhlB | ||
BNJPHLCL_00131 | 1.6e-213 | sucC | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
BNJPHLCL_00132 | 2.2e-165 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
BNJPHLCL_00133 | 1.2e-160 | dprA | LU | Rossmann fold nucleotide-binding protein involved in DNA uptake | ||
BNJPHLCL_00137 | 1.6e-08 | |||||
BNJPHLCL_00138 | 4e-08 | |||||
BNJPHLCL_00144 | 3e-09 | |||||
BNJPHLCL_00154 | 9.4e-164 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
BNJPHLCL_00155 | 7.9e-252 | menF | 5.4.4.2 | HQ | Isochorismate synthase | |
BNJPHLCL_00156 | 0.0 | menD | 2.2.1.9 | H | Catalyzes the thiamine diphosphate-dependent decarboxylation of 2-oxoglutarate and the subsequent addition of the resulting succinic semialdehyde-thiamine pyrophosphate anion to isochorismate to yield 2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylate (SEPHCHC) | |
BNJPHLCL_00157 | 7.7e-154 | menH | 4.2.99.20 | S | Catalyzes a proton abstraction reaction that results in 2,5-elimination of pyruvate from 2-succinyl-5-enolpyruvyl-6- hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC) and the formation of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) | |
BNJPHLCL_00158 | 1.9e-155 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
BNJPHLCL_00159 | 2.4e-278 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
BNJPHLCL_00160 | 4.7e-210 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
BNJPHLCL_00161 | 4.8e-23 | S | Domain of Unknown Function (DUF1540) | |||
BNJPHLCL_00162 | 3.4e-158 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
BNJPHLCL_00164 | 6.4e-40 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
BNJPHLCL_00165 | 3.6e-76 | dps | P | Belongs to the Dps family | ||
BNJPHLCL_00166 | 7.4e-39 | |||||
BNJPHLCL_00167 | 9.8e-85 | ytkD | 3.6.1.55 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
BNJPHLCL_00168 | 1.2e-127 | ytlD | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
BNJPHLCL_00169 | 2.3e-139 | ytlC | P | ABC transporter | ||
BNJPHLCL_00170 | 5.6e-186 | ytlA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
BNJPHLCL_00171 | 8.4e-54 | gntK | 2.7.1.12, 2.7.1.17 | G | FGGY family of carbohydrate kinases, N-terminal domain | |
BNJPHLCL_00172 | 2.3e-101 | ywqN | S | NAD(P)H-dependent | ||
BNJPHLCL_00173 | 1.9e-208 | ytmA | E | COG1506 Dipeptidyl aminopeptidases acylaminoacyl-peptidases | ||
BNJPHLCL_00174 | 1.1e-15 | S | Ribbon-helix-helix protein, copG family | |||
BNJPHLCL_00175 | 1.2e-306 | ggtA | 2.3.2.2, 3.4.19.13 | E | gamma-glutamyltransferase | |
BNJPHLCL_00176 | 1.3e-96 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
BNJPHLCL_00177 | 7.9e-55 | fliT | S | bacterial-type flagellum organization | ||
BNJPHLCL_00178 | 1.1e-68 | fliS | N | flagellar protein FliS | ||
BNJPHLCL_00179 | 0.0 | fliD | N | morphogenesis and for the elongation of the flagellar filament by facilitating polymerization of the flagellin monomers at the tip of growing filament. Forms a capping structure, which prevents flagellin subunits (transported through the central channel of the flagellum) from leaking out without polymerization at the distal end | ||
BNJPHLCL_00180 | 7.8e-61 | flaG | N | flagellar protein FlaG | ||
BNJPHLCL_00182 | 3e-110 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
BNJPHLCL_00183 | 2.5e-44 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase | |
BNJPHLCL_00184 | 1.4e-72 | S | Threonine/Serine exporter, ThrE | |||
BNJPHLCL_00185 | 2.6e-127 | thrE | S | Putative threonine/serine exporter | ||
BNJPHLCL_00186 | 2.1e-207 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
BNJPHLCL_00187 | 0.0 | cstA | T | Carbon starvation protein | ||
BNJPHLCL_00188 | 2.1e-154 | metQ | M | Belongs to the nlpA lipoprotein family | ||
BNJPHLCL_00189 | 2.9e-98 | metI | P | COG2011 ABC-type metal ion transport system, permease component | ||
BNJPHLCL_00190 | 3.3e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
BNJPHLCL_00191 | 6.2e-140 | modF | 3.6.3.21, 3.6.3.34 | P | COG1119 ABC-type molybdenum transport system, ATPase component photorepair protein PhrA | |
BNJPHLCL_00192 | 4e-96 | |||||
BNJPHLCL_00193 | 1.8e-220 | pilM | NU | Pilus assembly protein | ||
BNJPHLCL_00194 | 3.1e-240 | yisQ | V | Mate efflux family protein | ||
BNJPHLCL_00195 | 6.5e-153 | M | Glycosyl transferase family 8 | |||
BNJPHLCL_00196 | 3.7e-232 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
BNJPHLCL_00199 | 2.9e-271 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_00200 | 1.2e-09 | S | Leucine-rich repeat (LRR) protein | |||
BNJPHLCL_00201 | 2.1e-225 | uraA | F | Xanthine uracil | ||
BNJPHLCL_00202 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BNJPHLCL_00203 | 1.1e-214 | L | PFAM Transposase, IS116 IS110 IS902 | |||
BNJPHLCL_00204 | 2.5e-74 | MA20_02285 | 2.3.1.57 | K | Acetyltransferase (GNAT) family | |
BNJPHLCL_00205 | 2.4e-28 | VPA1573 | J | acetyltransferase | ||
BNJPHLCL_00206 | 7.2e-86 | yvbK | 3.1.3.25 | K | acetyltransferase | |
BNJPHLCL_00207 | 2.8e-117 | spoIISA | S | Toxin SpoIISA, type II toxin-antitoxin system | ||
BNJPHLCL_00209 | 6.5e-93 | sipT | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
BNJPHLCL_00210 | 1.1e-198 | yrpB | 1.13.12.16 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | |
BNJPHLCL_00213 | 7.8e-55 | E | Glyoxalase | |||
BNJPHLCL_00214 | 0.0 | ppdK | 2.7.3.13, 2.7.9.1 | G | Belongs to the PEP-utilizing enzyme family | |
BNJPHLCL_00215 | 2.9e-148 | yqfL | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
BNJPHLCL_00216 | 3.2e-215 | yjjL | G | Major facilitator superfamily | ||
BNJPHLCL_00217 | 6.3e-145 | |||||
BNJPHLCL_00218 | 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 | |
BNJPHLCL_00219 | 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 | |
BNJPHLCL_00220 | 1.9e-71 | yccU | S | CoA-binding protein | ||
BNJPHLCL_00221 | 5e-97 | 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 | |
BNJPHLCL_00222 | 5.3e-52 | yneR | S | Belongs to the HesB IscA family | ||
BNJPHLCL_00223 | 7.1e-52 | yneQ | ||||
BNJPHLCL_00224 | 2.2e-75 | yneP | S | thioesterase | ||
BNJPHLCL_00225 | 4.1e-31 | tlp | S | Belongs to the Tlp family | ||
BNJPHLCL_00226 | 1.7e-19 | sspN | S | Small acid-soluble spore protein N family | ||
BNJPHLCL_00228 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
BNJPHLCL_00229 | 4.4e-18 | sspO | S | Belongs to the SspO family | ||
BNJPHLCL_00230 | 7.1e-239 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
BNJPHLCL_00231 | 4.5e-39 | |||||
BNJPHLCL_00232 | 8.6e-19 | sspP | S | Belongs to the SspP family | ||
BNJPHLCL_00233 | 1.1e-08 | S | membrane | |||
BNJPHLCL_00234 | 4.4e-109 | M | lytic transglycosylase activity | |||
BNJPHLCL_00235 | 0.0 | alkK | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
BNJPHLCL_00236 | 8.9e-111 | M | effector of murein hydrolase | |||
BNJPHLCL_00237 | 3.8e-61 | S | Increases the activity of extracellular murein hydrolases possibly by mediating their export via hole formation. Inhibited by the antiholin-like proteins LrgAB. In an unstressed cell, the LrgAB products probably inhibit the function of the CidA protein. When a cell is stressed by the addition of antibiotics or by other factors in the environment, CidA possibly oligomerizes within the bacterial cell membrane, creating lesions that disrupt the proton motive force, which in turn results in loss of cell viability. These lesions are also hypothesized to regulate the subsequent cell lysis by either allowing the murein hydrolases access to the cell wall substrate and or regulating their activity by a | |||
BNJPHLCL_00238 | 9.4e-43 | S | Small, acid-soluble spore proteins, alpha/beta type | |||
BNJPHLCL_00239 | 0.0 | yheH | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
BNJPHLCL_00240 | 0.0 | yheI | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
BNJPHLCL_00241 | 1.3e-48 | iscA | S | Heme biosynthesis protein HemY | ||
BNJPHLCL_00242 | 8.2e-233 | ywoD | EGP | Major facilitator superfamily | ||
BNJPHLCL_00243 | 8.3e-191 | yetN | S | Protein of unknown function (DUF3900) | ||
BNJPHLCL_00244 | 2.3e-230 | yifK | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
BNJPHLCL_00245 | 1.6e-128 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNJPHLCL_00246 | 1.8e-184 | bceS | 2.7.13.3 | T | Signal transduction histidine kinase | |
BNJPHLCL_00247 | 1.2e-135 | bceA | V | ABC transporter, ATP-binding protein | ||
BNJPHLCL_00248 | 0.0 | bceB | V | ABC transporter (permease) | ||
BNJPHLCL_00249 | 5.2e-47 | yxiS | ||||
BNJPHLCL_00250 | 2.8e-45 | S | Protein of unknown function (DUF1292) | |||
BNJPHLCL_00251 | 1e-173 | trxB_2 | 1.8.1.9 | C | FAD dependent oxidoreductase | |
BNJPHLCL_00252 | 3.2e-118 | folE | 3.5.4.16 | H | GTP cyclohydrolase | |
BNJPHLCL_00253 | 2.7e-31 | cspB | K | Cold shock | ||
BNJPHLCL_00255 | 7.7e-102 | 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 | |
BNJPHLCL_00256 | 4.7e-24 | S | ATP synthase, subunit b | |||
BNJPHLCL_00257 | 2.1e-310 | ubiB | S | ABC1 family | ||
BNJPHLCL_00258 | 5.2e-215 | yeaN | P | COG2807 Cyanate permease | ||
BNJPHLCL_00259 | 1.1e-44 | yxcD | S | Protein of unknown function (DUF2653) | ||
BNJPHLCL_00260 | 4.6e-15 | |||||
BNJPHLCL_00261 | 8.3e-134 | ykrK | S | Domain of unknown function (DUF1836) | ||
BNJPHLCL_00262 | 3.3e-121 | P | COG0569 K transport systems, NAD-binding component | |||
BNJPHLCL_00263 | 6.5e-219 | ktrB | P | COG0168 Trk-type K transport systems, membrane components | ||
BNJPHLCL_00264 | 6.1e-161 | rarD | S | -transporter | ||
BNJPHLCL_00265 | 1.8e-239 | yedE | S | Sulphur transport | ||
BNJPHLCL_00266 | 1.7e-40 | yedF | O | Belongs to the sulfur carrier protein TusA family | ||
BNJPHLCL_00267 | 3.1e-116 | hisE | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | belongs to the PRA-CH family | |
BNJPHLCL_00268 | 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 | |
BNJPHLCL_00269 | 2.4e-127 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
BNJPHLCL_00270 | 6.1e-111 | 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 | ||
BNJPHLCL_00271 | 2.9e-105 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
BNJPHLCL_00272 | 3.3e-231 | 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 | |
BNJPHLCL_00273 | 1.8e-110 | hisG | 2.4.2.17 | E | 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 | |
BNJPHLCL_00274 | 1.3e-218 | 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 | |
BNJPHLCL_00275 | 2.7e-63 | S | CHY zinc finger | |||
BNJPHLCL_00276 | 1.2e-177 | corA | P | Mg2 transporter protein | ||
BNJPHLCL_00277 | 3.5e-247 | ycgH | E | COG1113 Gamma-aminobutyrate permease and related permeases | ||
BNJPHLCL_00278 | 0.0 | topB2 | 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 | |
BNJPHLCL_00279 | 1.5e-101 | yocH | CBM50 | M | COG1388 FOG LysM repeat | |
BNJPHLCL_00280 | 7.8e-55 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
BNJPHLCL_00281 | 2.4e-101 | yhfW | CE | COG0665 Glycine D-amino acid oxidases (deaminating) | ||
BNJPHLCL_00282 | 2.1e-79 | S | Domain in cystathionine beta-synthase and other proteins. | |||
BNJPHLCL_00283 | 1.2e-168 | yflN | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
BNJPHLCL_00284 | 2.9e-105 | thiT | S | Proton-coupled thiamine transporter YuaJ | ||
BNJPHLCL_00285 | 1.1e-129 | yoqW | S | Belongs to the SOS response-associated peptidase family | ||
BNJPHLCL_00286 | 3.5e-193 | yceA | S | Belongs to the UPF0176 family | ||
BNJPHLCL_00287 | 0.0 | topB | 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 | |
BNJPHLCL_00288 | 5.2e-159 | yqfU | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
BNJPHLCL_00290 | 1.4e-115 | 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 | ||
BNJPHLCL_00291 | 3.8e-83 | rok | S | Repressor of ComK | ||
BNJPHLCL_00292 | 1.7e-287 | dhaS | 1.2.1.3, 1.2.1.39 | C | Belongs to the aldehyde dehydrogenase family | |
BNJPHLCL_00293 | 8.4e-203 | sucB | 2.3.1.61 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2) | |
BNJPHLCL_00294 | 0.0 | sucA | 1.2.4.2, 4.1.1.71 | C | The 2-oxoglutarate dehydrogenase complex catalyzes the overall conversion of 2-oxoglutarate to succinyl-CoA and CO(2). It contains multiple copies of three enzymatic components 2- oxoglutarate dehydrogenase (E1), dihydrolipoamide succinyltransferase (E2) and lipoamide dehydrogenase (E3) | |
BNJPHLCL_00295 | 1.5e-74 | yozR | S | COG0071 Molecular chaperone (small heat shock protein) | ||
BNJPHLCL_00296 | 6.9e-220 | ykoN | 2.4.1.315 | GT28 | M | COG0707 UDP-N-acetylglucosamine LPS N-acetylglucosamine transferase |
BNJPHLCL_00297 | 1.3e-88 | K | Belongs to the sigma-70 factor family. ECF subfamily | |||
BNJPHLCL_00298 | 1.5e-83 | S | Putative zinc-finger | |||
BNJPHLCL_00299 | 2.3e-47 | |||||
BNJPHLCL_00300 | 4e-270 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
BNJPHLCL_00303 | 9.4e-280 | yobO | M | Pectate lyase superfamily protein | ||
BNJPHLCL_00304 | 1.1e-07 | |||||
BNJPHLCL_00305 | 4.2e-143 | cysH | 1.8.4.10, 1.8.4.8, 2.7.1.25 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
BNJPHLCL_00306 | 2.3e-144 | hemD | 2.1.1.107, 4.2.1.75 | H | Belongs to the precorrin methyltransferase family | |
BNJPHLCL_00307 | 6.3e-126 | cbiX | 4.99.1.3, 4.99.1.4, 5.4.99.60, 5.4.99.61 | S | Sirohydrochlorin ferrochelatase | |
BNJPHLCL_00308 | 1.7e-103 | cysG | 1.3.1.76, 4.99.1.4 | H | Siroheme synthase | |
BNJPHLCL_00309 | 3.1e-95 | ywhH | S | Aminoacyl-tRNA editing domain | ||
BNJPHLCL_00310 | 6.5e-204 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
BNJPHLCL_00311 | 3.4e-13 | S | PFAM Uncharacterised protein family UPF0236 | |||
BNJPHLCL_00312 | 2.8e-309 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |||
BNJPHLCL_00314 | 2.6e-169 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
BNJPHLCL_00316 | 1.7e-178 | S | Nuclease-related domain | |||
BNJPHLCL_00317 | 9e-89 | |||||
BNJPHLCL_00318 | 7.3e-172 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
BNJPHLCL_00319 | 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 | |
BNJPHLCL_00320 | 7.9e-293 | M | Glycosyltransferase like family 2 | |||
BNJPHLCL_00321 | 1.6e-171 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases C terminal | |
BNJPHLCL_00322 | 6.9e-181 | mvaD | 4.1.1.33 | I | GHMP kinases N terminal domain | |
BNJPHLCL_00323 | 1.6e-202 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases C terminal | |
BNJPHLCL_00324 | 2e-112 | yhfK | GM | NmrA-like family | ||
BNJPHLCL_00325 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
BNJPHLCL_00326 | 8e-145 | ywfI | C | May function as heme-dependent peroxidase | ||
BNJPHLCL_00327 | 4.3e-175 | pta | 2.3.1.8, 3.6.3.21 | C | In Salmonella this enzyme is required for ethanolamine catabolism | |
BNJPHLCL_00329 | 1.8e-153 | lipL | 2.3.1.200, 2.3.1.204 | H | Catalyzes the amidotransfer (transamidation) of the octanoyl moiety from octanoyl-GcvH to the lipoyl domain of the E2 subunit of lipoate-dependent enzymes | |
BNJPHLCL_00330 | 5.7e-100 | rsfA | S | Transcriptional regulator | ||
BNJPHLCL_00331 | 6.1e-257 | ywfO | S | COG1078 HD superfamily phosphohydrolases | ||
BNJPHLCL_00332 | 8.7e-90 | ywgA | 2.1.1.72, 3.1.21.3 | |||
BNJPHLCL_00333 | 2.7e-25 | dmpI | 5.3.2.6 | G | 4-oxalocrotonate tautomerase | |
BNJPHLCL_00334 | 6.6e-119 | ywhC | S | Peptidase M50 | ||
BNJPHLCL_00335 | 1.7e-93 | ywhD | S | YwhD family | ||
BNJPHLCL_00336 | 0.0 | pbpG | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BNJPHLCL_00337 | 4.1e-169 | speB | 3.5.3.11 | E | Belongs to the arginase family | |
BNJPHLCL_00338 | 1.1e-74 | ywiB | S | Domain of unknown function (DUF1934) | ||
BNJPHLCL_00339 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
BNJPHLCL_00340 | 2.7e-211 | cls | I | Belongs to the phospholipase D family. Cardiolipin synthase subfamily | ||
BNJPHLCL_00341 | 0.0 | fadF | C | COG0247 Fe-S oxidoreductase | ||
BNJPHLCL_00342 | 2.9e-218 | mmgA | 2.3.1.9 | I | Catalyzes the synthesis of acetoacetyl coenzyme A from two molecules of acetyl coenzyme A. It can also act as a thiolase, catalyzing the reverse reaction and generating two-carbon units from the four-carbon product of fatty acid oxidation | |
BNJPHLCL_00343 | 2e-208 | mmgC | I | acyl-CoA dehydrogenase | ||
BNJPHLCL_00344 | 3.2e-214 | acdA | 1.3.8.1, 1.3.8.7 | I | acyl-CoA dehydrogenase | |
BNJPHLCL_00345 | 1.3e-111 | kstR2_2 | K | Transcriptional regulator | ||
BNJPHLCL_00346 | 1.1e-40 | icmF | 5.4.99.13 | EI | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | |
BNJPHLCL_00347 | 5.1e-131 | icmF | 5.4.99.13 | EI | Catalyzes the reversible interconversion of isobutyryl- CoA and n-butyryl-CoA, using radical chemistry. Also exhibits GTPase activity, associated with its G-protein domain (MeaI) that functions as a chaperone that assists cofactor delivery and proper holo-enzyme assembly | |
BNJPHLCL_00349 | 7.7e-50 | 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 | ||
BNJPHLCL_00350 | 9.8e-310 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
BNJPHLCL_00351 | 2e-65 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
BNJPHLCL_00352 | 3.8e-114 | yhcG | V | ABC transporter, ATP-binding protein | ||
BNJPHLCL_00356 | 5.6e-247 | 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 | |
BNJPHLCL_00357 | 2.2e-249 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BNJPHLCL_00358 | 5.3e-72 | rplI | J | binds to the 23S rRNA | ||
BNJPHLCL_00359 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
BNJPHLCL_00360 | 4.6e-158 | yybS | S | membrane | ||
BNJPHLCL_00361 | 3e-37 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
BNJPHLCL_00362 | 3.2e-81 | 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 | ||
BNJPHLCL_00363 | 5e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
BNJPHLCL_00364 | 1.6e-79 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
BNJPHLCL_00365 | 2.2e-221 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of D-ribulose 5-phosphate to formate and 3,4-dihydroxy-2-butanone 4-phosphate | |
BNJPHLCL_00366 | 1.6e-117 | ribE | 2.5.1.9 | H | Riboflavin synthase | |
BNJPHLCL_00367 | 4e-209 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
BNJPHLCL_00368 | 1.9e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BNJPHLCL_00369 | 1.1e-32 | yyzM | S | protein conserved in bacteria | ||
BNJPHLCL_00370 | 5.9e-158 | ykuT | M | Mechanosensitive ion channel | ||
BNJPHLCL_00371 | 1.5e-112 | yyaC | S | Sporulation protein YyaC | ||
BNJPHLCL_00372 | 3.2e-119 | ydfK | S | Protein of unknown function (DUF554) | ||
BNJPHLCL_00373 | 5e-151 | spo0J | K | Belongs to the ParB family | ||
BNJPHLCL_00374 | 6.9e-136 | soj | D | COG1192 ATPases involved in chromosome partitioning | ||
BNJPHLCL_00375 | 9.1e-153 | noc | D | Effects nucleoid occlusion by binding relatively nonspecifically to DNA and preventing the assembly of the division machinery in the vicinity of the nucleoid, especially under conditions that disturb the cell cycle. It helps to coordinate cell division and chromosome segregation by preventing the formation of the Z ring through the nucleoid, which would cause chromosome breakage | ||
BNJPHLCL_00376 | 7.4e-132 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of guanine in position 535 of 16S rRNA | |
BNJPHLCL_00377 | 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 | ||
BNJPHLCL_00378 | 5.3e-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 | ||
BNJPHLCL_00379 | 1.3e-108 | jag | S | single-stranded nucleic acid binding R3H | ||
BNJPHLCL_00380 | 3.2e-128 | 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 | ||
BNJPHLCL_00381 | 4.2e-56 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
BNJPHLCL_00382 | 9e-256 | 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 | ||
BNJPHLCL_00383 | 1e-207 | 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 | |
BNJPHLCL_00384 | 4.6e-238 | 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 | |
BNJPHLCL_00385 | 1e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
BNJPHLCL_00386 | 8e-53 | atpI | S | ATP synthase I chain | ||
BNJPHLCL_00387 | 8.2e-131 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
BNJPHLCL_00388 | 1.3e-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 | ||
BNJPHLCL_00389 | 1.3e-37 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
BNJPHLCL_00390 | 4.9e-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 | ||
BNJPHLCL_00391 | 5.9e-280 | 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 | |
BNJPHLCL_00392 | 4.7e-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 | ||
BNJPHLCL_00393 | 4.5e-266 | 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 | |
BNJPHLCL_00394 | 1.8e-53 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
BNJPHLCL_00395 | 6.8e-34 | ywzB | S | membrane | ||
BNJPHLCL_00396 | 1.1e-135 | ywmB | S | TATA-box binding | ||
BNJPHLCL_00397 | 4.8e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BNJPHLCL_00398 | 1.2e-08 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BNJPHLCL_00399 | 8.1e-185 | spoIID | D | Stage II sporulation protein D | ||
BNJPHLCL_00400 | 1.8e-128 | spoIIQ | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
BNJPHLCL_00401 | 6.5e-41 | spoIIID | K | Stage III sporulation protein D | ||
BNJPHLCL_00402 | 1.9e-178 | mbl | D | Rod shape-determining protein | ||
BNJPHLCL_00403 | 5.4e-144 | flhO | N | flagellar basal body | ||
BNJPHLCL_00404 | 1.9e-139 | flhP | N | flagellar basal body | ||
BNJPHLCL_00405 | 8.7e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
BNJPHLCL_00407 | 3.3e-64 | ssbB | L | Single-stranded DNA-binding protein | ||
BNJPHLCL_00408 | 1.9e-71 | ywpF | S | YwpF-like protein | ||
BNJPHLCL_00410 | 0.0 | ywqA | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
BNJPHLCL_00411 | 1.3e-306 | ywqB | S | Zinc finger, swim domain protein | ||
BNJPHLCL_00412 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
BNJPHLCL_00413 | 2.3e-31 | gerE | K | Transcriptional regulator | ||
BNJPHLCL_00414 | 6.7e-89 | ysmA | S | thioesterase | ||
BNJPHLCL_00415 | 6.5e-150 | sdhB | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
BNJPHLCL_00416 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | succinate dehydrogenase | |
BNJPHLCL_00417 | 2.5e-104 | sdhC | C | succinate dehydrogenase | ||
BNJPHLCL_00418 | 3e-78 | yslB | S | Protein of unknown function (DUF2507) | ||
BNJPHLCL_00419 | 2e-222 | lysC | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
BNJPHLCL_00420 | 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 | ||
BNJPHLCL_00421 | 5.1e-53 | trxA | O | Belongs to the thioredoxin family | ||
BNJPHLCL_00422 | 7.4e-175 | etfA | C | Electron transfer flavoprotein | ||
BNJPHLCL_00423 | 4.8e-129 | etfB | C | Electron transfer flavoprotein | ||
BNJPHLCL_00424 | 1.5e-138 | fadB | 4.2.1.17 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
BNJPHLCL_00425 | 6e-103 | fadR | K | Transcriptional regulator | ||
BNJPHLCL_00426 | 0.0 | lcfA | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | |
BNJPHLCL_00427 | 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 | ||
BNJPHLCL_00428 | 0.0 | polX | L | COG1796 DNA polymerase IV (family X) | ||
BNJPHLCL_00429 | 1.9e-87 | cvpA | S | membrane protein, required for colicin V production | ||
BNJPHLCL_00430 | 7.3e-46 | 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 | ||
BNJPHLCL_00431 | 9.9e-169 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BNJPHLCL_00432 | 5.7e-45 | KT | Transcriptional | |||
BNJPHLCL_00433 | 1.2e-31 | V | Mate efflux family protein | |||
BNJPHLCL_00434 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BNJPHLCL_00435 | 9.6e-181 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
BNJPHLCL_00436 | 8.9e-136 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BNJPHLCL_00437 | 6.4e-31 | sspI | S | Belongs to the SspI family | ||
BNJPHLCL_00438 | 2.2e-134 | |||||
BNJPHLCL_00439 | 2.5e-29 | sidE | D | nuclear chromosome segregation | ||
BNJPHLCL_00440 | 2.7e-285 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BNJPHLCL_00443 | 1.1e-97 | 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 | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
BNJPHLCL_00444 | 6e-61 | 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 | |
BNJPHLCL_00445 | 1.7e-156 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
BNJPHLCL_00446 | 8.9e-170 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
BNJPHLCL_00447 | 8.4e-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 | ||
BNJPHLCL_00448 | 1.7e-159 | coaX | 2.7.1.33 | F | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
BNJPHLCL_00449 | 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 | ||
BNJPHLCL_00450 | 2.9e-96 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
BNJPHLCL_00451 | 4e-278 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
BNJPHLCL_00452 | 2.8e-166 | KLT | serine threonine protein kinase | |||
BNJPHLCL_00453 | 8.7e-120 | yabS | S | protein containing a von Willebrand factor type A (vWA) domain | ||
BNJPHLCL_00454 | 0.0 | spoIIE | 3.1.3.16, 3.1.3.3 | KT | stage II sporulation protein E | |
BNJPHLCL_00456 | 3.7e-54 | yabR | J | RNA binding protein (contains ribosomal protein S1 domain) | ||
BNJPHLCL_00457 | 1.9e-60 | divIC | D | Septum formation initiator | ||
BNJPHLCL_00458 | 8e-106 | yabQ | S | spore cortex biosynthesis protein | ||
BNJPHLCL_00459 | 3e-50 | yabP | S | Sporulation protein YabP | ||
BNJPHLCL_00460 | 2.4e-41 | yabO | J | COG1188 Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
BNJPHLCL_00461 | 3.1e-190 | mazG | 3.6.1.66, 3.6.1.9 | S | COG3956 Protein containing tetrapyrrole methyltransferase domain and MazG-like | |
BNJPHLCL_00462 | 2.1e-275 | yabM | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
BNJPHLCL_00463 | 2.1e-91 | spoVT | K | stage V sporulation protein | ||
BNJPHLCL_00464 | 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 | ||
BNJPHLCL_00465 | 1.8e-36 | yabK | S | Peptide ABC transporter permease | ||
BNJPHLCL_00466 | 2.7e-105 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
BNJPHLCL_00467 | 1.7e-108 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
BNJPHLCL_00468 | 1.2e-174 | 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) | |
BNJPHLCL_00469 | 1.2e-242 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
BNJPHLCL_00471 | 1.4e-47 | spoVG | D | Essential for sporulation. Interferes with or is a negative regulator of the pathway leading to asymmetric septation | ||
BNJPHLCL_00472 | 1.2e-61 | yabJ | 3.5.99.10 | J | translation initiation inhibitor, yjgF family | |
BNJPHLCL_00473 | 1.3e-152 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
BNJPHLCL_00474 | 7.3e-158 | ispE | 2.1.1.182, 2.7.1.148 | I | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
BNJPHLCL_00475 | 1.9e-26 | sspF | S | DNA topological change | ||
BNJPHLCL_00476 | 2.4e-37 | veg | S | protein conserved in bacteria | ||
BNJPHLCL_00477 | 6.4e-162 | yabG | S | peptidase | ||
BNJPHLCL_00478 | 2.7e-160 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
BNJPHLCL_00479 | 5e-105 | 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 | |
BNJPHLCL_00480 | 8e-148 | tatD | L | hydrolase, TatD | ||
BNJPHLCL_00481 | 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 | |
BNJPHLCL_00482 | 4.8e-55 | abrB | K | COG2002 Regulators of stationary sporulation gene expression | ||
BNJPHLCL_00483 | 2.6e-163 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
BNJPHLCL_00484 | 7.1e-49 | yazA | L | endonuclease containing a URI domain | ||
BNJPHLCL_00485 | 1.6e-137 | yabB | 2.1.1.223 | S | Conserved hypothetical protein 95 | |
BNJPHLCL_00486 | 3.3e-61 | yabA | L | Involved in initiation control of chromosome replication | ||
BNJPHLCL_00487 | 1.7e-148 | yaaT | S | stage 0 sporulation protein | ||
BNJPHLCL_00488 | 6.8e-184 | holB | 2.7.7.7 | L | DNA polymerase III | |
BNJPHLCL_00489 | 1.5e-71 | yaaR | S | protein conserved in bacteria | ||
BNJPHLCL_00490 | 9.8e-55 | yaaQ | S | protein conserved in bacteria | ||
BNJPHLCL_00491 | 2.3e-119 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
BNJPHLCL_00492 | 1.4e-281 | adiA | 4.1.1.17, 4.1.1.18, 4.1.1.19 | E | Orn Lys Arg decarboxylase | |
BNJPHLCL_00493 | 2.4e-30 | csfB | S | Inhibitor of sigma-G Gin | ||
BNJPHLCL_00495 | 0.0 | ycbZ | 3.4.21.53 | O | AAA domain | |
BNJPHLCL_00496 | 1.3e-169 | E | COG1113 Gamma-aminobutyrate permease and related permeases | |||
BNJPHLCL_00498 | 1.5e-245 | EGP | Sugar (and other) transporter | |||
BNJPHLCL_00499 | 7.5e-146 | G | myo-inosose-2 dehydratase activity | |||
BNJPHLCL_00500 | 3.2e-155 | araL | 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
BNJPHLCL_00501 | 8e-115 | sapB | S | MgtC SapB transporter | ||
BNJPHLCL_00502 | 5.5e-98 | K | Glycerol-3-phosphate responsive antiterminator | |||
BNJPHLCL_00503 | 2.4e-84 | fliC | N | Flagellin is the subunit protein which polymerizes to form the filaments of bacterial flagella | ||
BNJPHLCL_00504 | 2.4e-34 | csrA | T | Could accelerate the degradation of some genes transcripts potentially through selective RNA binding | ||
BNJPHLCL_00505 | 3.6e-76 | fliW | S | Binds to the C-terminal region of flagellin, which is implicated in polymerization, and participates in the assembly of the flagellum | ||
BNJPHLCL_00506 | 4.3e-153 | flgL | N | Belongs to the bacterial flagellin family | ||
BNJPHLCL_00507 | 7.7e-286 | flgK | N | flagellar hook-associated protein | ||
BNJPHLCL_00508 | 5.9e-69 | flgN | NOU | FlgN protein | ||
BNJPHLCL_00509 | 1e-38 | flgM | KNU | Negative regulator of flagellin synthesis | ||
BNJPHLCL_00510 | 2.1e-67 | yvyF | S | flagellar protein | ||
BNJPHLCL_00511 | 1.5e-132 | comFC | S | Phosphoribosyl transferase domain | ||
BNJPHLCL_00512 | 1.9e-253 | comFA | L | COG4098 Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
BNJPHLCL_00513 | 1.5e-152 | degV | S | protein conserved in bacteria | ||
BNJPHLCL_00514 | 2.4e-259 | yfnA | E | amino acid | ||
BNJPHLCL_00515 | 4.9e-125 | degU | KT | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
BNJPHLCL_00516 | 1.3e-205 | degS | 2.7.13.3 | T | Member of the two-component regulatory system DegS DegU, which plays an important role in the transition growth phase | |
BNJPHLCL_00517 | 1.1e-115 | yvyE | 3.4.13.9 | S | Domain of unknown function (DUF1949) | |
BNJPHLCL_00518 | 2.4e-168 | tagO | 2.7.8.33, 2.7.8.35 | M | COG0472 UDP-N-acetylmuramyl pentapeptide phosphotransferase UDP-N-acetylglucosamine-1-phosphate transferase | |
BNJPHLCL_00519 | 0.0 | pbpC | 3.4.16.4 | M | Penicillin-binding Protein | |
BNJPHLCL_00520 | 1e-239 | NT | Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). | |||
BNJPHLCL_00521 | 3.2e-170 | sle1 | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
BNJPHLCL_00522 | 4.3e-124 | gntR1 | K | transcriptional | ||
BNJPHLCL_00523 | 8.9e-133 | 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 | |
BNJPHLCL_00524 | 1.4e-214 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
BNJPHLCL_00525 | 1.2e-274 | yusP | P | Major facilitator superfamily | ||
BNJPHLCL_00526 | 3.5e-07 | yusP | P | Major facilitator superfamily | ||
BNJPHLCL_00527 | 2.8e-176 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
BNJPHLCL_00528 | 3.9e-189 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
BNJPHLCL_00529 | 5.8e-70 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
BNJPHLCL_00530 | 2.6e-163 | cvfB | S | protein conserved in bacteria | ||
BNJPHLCL_00532 | 5.4e-75 | P | nitrite transmembrane transporter activity | |||
BNJPHLCL_00534 | 3.1e-93 | |||||
BNJPHLCL_00535 | 5.5e-193 | L | Transposase DDE domain group 1 | |||
BNJPHLCL_00536 | 2.7e-170 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | |||
BNJPHLCL_00537 | 9.6e-138 | fecE | 3.6.3.34 | HP | ABC transporter | |
BNJPHLCL_00538 | 1.9e-189 | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | |||
BNJPHLCL_00539 | 2.9e-30 | ybxH | S | Family of unknown function (DUF5370) | ||
BNJPHLCL_00540 | 1.5e-08 | |||||
BNJPHLCL_00541 | 4.9e-173 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_00542 | 1.1e-214 | yihS | 5.1.3.11, 5.3.1.9 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
BNJPHLCL_00543 | 1.9e-192 | yeeE | S | Sulphur transport | ||
BNJPHLCL_00544 | 6.9e-36 | yeeD | O | Belongs to the sulfur carrier protein TusA family | ||
BNJPHLCL_00545 | 2.7e-158 | S | transposase or invertase | |||
BNJPHLCL_00546 | 9.5e-14 | S | transposase or invertase | |||
BNJPHLCL_00547 | 1.1e-14 | S | transposase or invertase | |||
BNJPHLCL_00548 | 9.8e-64 | argO | S | Lysine exporter protein LysE YggA | ||
BNJPHLCL_00549 | 8.8e-281 | yisV | K | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
BNJPHLCL_00550 | 3.2e-16 | yeeD | O | Belongs to the sulfur carrier protein TusA family | ||
BNJPHLCL_00551 | 1.1e-31 | rcfB | K | Bacterial regulatory proteins, crp family | ||
BNJPHLCL_00552 | 1.3e-23 | L | Transposase IS66 family | |||
BNJPHLCL_00553 | 5.5e-13 | |||||
BNJPHLCL_00554 | 6.4e-91 | S | ABC-2 family transporter protein | |||
BNJPHLCL_00555 | 1.2e-82 | prrC | P | ABC transporter | ||
BNJPHLCL_00556 | 8.7e-99 | yydH | O | Peptidase M50 | ||
BNJPHLCL_00557 | 2.7e-156 | S | Radical SAM superfamily | |||
BNJPHLCL_00558 | 3.9e-11 | |||||
BNJPHLCL_00559 | 9.9e-71 | ywnA | K | Transcriptional regulator | ||
BNJPHLCL_00560 | 6.2e-114 | ywnB | S | NAD(P)H-binding | ||
BNJPHLCL_00561 | 5.1e-95 | padC | Q | Phenolic acid decarboxylase | ||
BNJPHLCL_00562 | 4.6e-97 | padR | K | transcriptional | ||
BNJPHLCL_00563 | 3.1e-57 | yhcF | K | Transcriptional regulator | ||
BNJPHLCL_00564 | 9e-122 | yhcG | V | ABC transporter, ATP-binding protein | ||
BNJPHLCL_00565 | 2.5e-56 | |||||
BNJPHLCL_00566 | 1.1e-135 | tnp | L | PFAM Transposase, Mutator | ||
BNJPHLCL_00567 | 1.9e-57 | |||||
BNJPHLCL_00568 | 1.5e-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 | |
BNJPHLCL_00569 | 6.2e-235 | 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 | |
BNJPHLCL_00570 | 2.3e-150 | yjaZ | O | Zn-dependent protease | ||
BNJPHLCL_00571 | 7.8e-191 | oppD | P | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_00572 | 1.3e-176 | oppF | P | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_00573 | 1.7e-168 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BNJPHLCL_00574 | 4.5e-134 | oppC | EP | binding-protein-dependent transport systems inner membrane component | ||
BNJPHLCL_00575 | 0.0 | oppA1 | E | COG0747 ABC-type dipeptide transport system, periplasmic component | ||
BNJPHLCL_00576 | 1.1e-146 | yjbA | S | Belongs to the UPF0736 family | ||
BNJPHLCL_00577 | 1e-184 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
BNJPHLCL_00578 | 8.3e-49 | S | Domain of unknown function (DUF3899) | |||
BNJPHLCL_00581 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
BNJPHLCL_00582 | 3.8e-182 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
BNJPHLCL_00583 | 1.2e-247 | citH | C | Citrate transporter | ||
BNJPHLCL_00584 | 4.6e-123 | citT | T | response regulator | ||
BNJPHLCL_00585 | 1.4e-295 | citS | 2.7.13.3 | T | Signal transduction histidine kinase regulating citrate malate metabolism | |
BNJPHLCL_00586 | 2.6e-233 | amt | P | Ammonium transporter | ||
BNJPHLCL_00587 | 8.6e-223 | yugJ | C | oxidoreductases, Fe-dependent alcohol dehydrogenase family | ||
BNJPHLCL_00588 | 1.5e-250 | E | Amino acid permease | |||
BNJPHLCL_00589 | 2.5e-135 | lutA | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
BNJPHLCL_00590 | 8.6e-273 | lutB | C | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. Has probably a role as an electron transporter during oxidation of L-lactate | ||
BNJPHLCL_00591 | 1e-133 | lutC | S | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source | ||
BNJPHLCL_00592 | 6.3e-252 | E | amino acid | |||
BNJPHLCL_00593 | 3.4e-250 | H | HemY protein | |||
BNJPHLCL_00594 | 9.8e-205 | potD | E | COG0687 Spermidine putrescine-binding periplasmic protein | ||
BNJPHLCL_00595 | 5.4e-139 | potC | E | COG1177 ABC-type spermidine putrescine transport system, permease component II | ||
BNJPHLCL_00596 | 1.8e-139 | potB | E | COG1176 ABC-type spermidine putrescine transport system, permease component I | ||
BNJPHLCL_00597 | 1.2e-210 | 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 | |
BNJPHLCL_00598 | 4.3e-98 | puuR | K | Cupin domain | ||
BNJPHLCL_00600 | 8.4e-279 | lysP | E | amino acid | ||
BNJPHLCL_00601 | 4.8e-274 | dtpT | E | amino acid peptide transporter | ||
BNJPHLCL_00603 | 3.6e-93 | yqjB | S | protein conserved in bacteria | ||
BNJPHLCL_00604 | 2.1e-76 | yqiW | S | Belongs to the UPF0403 family | ||
BNJPHLCL_00605 | 3.4e-166 | fruK | 2.7.1.11, 2.7.1.56 | G | Belongs to the carbohydrate kinase PfkB family | |
BNJPHLCL_00606 | 3e-216 | bfmBB | 2.3.1.168, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
BNJPHLCL_00607 | 3.9e-184 | bfmBAB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
BNJPHLCL_00608 | 5e-187 | bfmBAA | 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
BNJPHLCL_00609 | 1.5e-261 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
BNJPHLCL_00610 | 1.5e-208 | ldh | 1.4.1.9 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
BNJPHLCL_00611 | 9.9e-18 | T | transcription factor binding | |||
BNJPHLCL_00612 | 1.4e-56 | 1.1.1.169, 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | prephenate dehydrogenase (NADP+) activity | ||
BNJPHLCL_00613 | 4.4e-36 | yqzF | S | Protein of unknown function (DUF2627) | ||
BNJPHLCL_00614 | 7.7e-132 | yqiK | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
BNJPHLCL_00615 | 4.4e-138 | KT | May play the central regulatory role in sporulation. It may be an element of the effector pathway responsible for the activation of sporulation genes in response to nutritional stress. Spo0A may act in concert with spo0H (a sigma factor) to control the expression of some genes that are critical to the sporulation process | |||
BNJPHLCL_00616 | 2.7e-233 | rseP | 3.4.21.116 | M | Stage IV sporulation protein B | |
BNJPHLCL_00617 | 1.3e-291 | recN | L | May be involved in recombinational repair of damaged DNA | ||
BNJPHLCL_00618 | 9.2e-80 | argR | K | Regulates arginine biosynthesis genes | ||
BNJPHLCL_00619 | 8.5e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | rRNA methylase | |
BNJPHLCL_00620 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
BNJPHLCL_00621 | 2.9e-154 | 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 | |
BNJPHLCL_00622 | 3.1e-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 | |
BNJPHLCL_00623 | 3.5e-228 | 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 | |
BNJPHLCL_00624 | 1.6e-157 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
BNJPHLCL_00625 | 1.6e-64 | 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 | ||
BNJPHLCL_00626 | 1.1e-68 | yqhY | S | protein conserved in bacteria | ||
BNJPHLCL_00627 | 1.8e-256 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
BNJPHLCL_00628 | 6.8e-81 | 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 | |
BNJPHLCL_00629 | 8.2e-67 | spoIIIAH | S | SpoIIIAH-like protein | ||
BNJPHLCL_00630 | 6.6e-111 | spoIIIAG | S | stage III sporulation protein AG | ||
BNJPHLCL_00631 | 1.8e-105 | spoIIIAF | S | Stage III sporulation protein AF (Spore_III_AF) | ||
BNJPHLCL_00632 | 1.7e-173 | spoIIIAE | S | stage III sporulation protein AE | ||
BNJPHLCL_00633 | 2.3e-58 | spoIIIAD | S | Stage III sporulation protein AD | ||
BNJPHLCL_00634 | 1.4e-27 | spoIIIAC | S | stage III sporulation protein AC | ||
BNJPHLCL_00635 | 3.7e-85 | spoIIIAB | S | Stage III sporulation protein | ||
BNJPHLCL_00636 | 8e-171 | spoIIIAA | S | stage III sporulation protein AA | ||
BNJPHLCL_00637 | 6.4e-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 | ||
BNJPHLCL_00638 | 5.4e-155 | yqhT | 3.4.11.9, 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
BNJPHLCL_00639 | 9.6e-77 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
BNJPHLCL_00640 | 3.1e-86 | yqhR | S | Conserved membrane protein YqhR | ||
BNJPHLCL_00641 | 2.7e-163 | yqhQ | S | Protein of unknown function (DUF1385) | ||
BNJPHLCL_00642 | 4.3e-11 | yqhP | ||||
BNJPHLCL_00643 | 5.6e-40 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
BNJPHLCL_00644 | 3e-79 | S | GDYXXLXY protein | |||
BNJPHLCL_00645 | 3.9e-78 | ysmB | 2.4.2.28 | K | transcriptional | |
BNJPHLCL_00646 | 6.2e-151 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BNJPHLCL_00648 | 1.5e-189 | gerM | S | COG5401 Spore germination protein | ||
BNJPHLCL_00649 | 6.6e-105 | rdgB | 3.6.1.66 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
BNJPHLCL_00650 | 7e-92 | ysnB | S | Phosphoesterase | ||
BNJPHLCL_00652 | 1.5e-46 | |||||
BNJPHLCL_00653 | 5.9e-71 | S | Protein of unknown function (DUF2512) | |||
BNJPHLCL_00654 | 6.8e-184 | trxA2 | O | COG0457 FOG TPR repeat | ||
BNJPHLCL_00655 | 8.4e-211 | 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 | ||
BNJPHLCL_00656 | 1.8e-234 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
BNJPHLCL_00657 | 1.5e-308 | lonB | 2.7.7.7, 3.4.21.53 | LO | Belongs to the peptidase S16 family | |
BNJPHLCL_00658 | 0.0 | lon | 3.4.21.53 | O | ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short-lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner | |
BNJPHLCL_00659 | 1.3e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
BNJPHLCL_00660 | 2.2e-87 | ysxD | ||||
BNJPHLCL_00661 | 2.1e-241 | hemA | 1.2.1.70 | H | Catalyzes the NADPH-dependent reduction of glutamyl- tRNA(Glu) to glutamate 1-semialdehyde (GSA) | |
BNJPHLCL_00662 | 1.7e-148 | hemX | O | cytochrome C | ||
BNJPHLCL_00663 | 3e-165 | hemC | 2.1.1.107, 2.5.1.61, 4.2.1.75 | H | Tetrapolymerization of the monopyrrole PBG into the hydroxymethylbilane pre-uroporphyrinogen in several discrete steps | |
BNJPHLCL_00664 | 1.9e-144 | hemD | 2.1.1.107, 4.2.1.75 | H | Uroporphyrinogen-III synthase | |
BNJPHLCL_00665 | 7.1e-186 | hemB | 4.2.1.24 | H | Belongs to the ALAD family | |
BNJPHLCL_00666 | 3.5e-249 | hemL | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
BNJPHLCL_00667 | 2e-200 | spoVID | M | stage VI sporulation protein D | ||
BNJPHLCL_00668 | 1.7e-190 | ysxE | S | A protein kinase that phosphorylates Ser and Thr residues. Probably acts to suppress the effects of stress linked to accumulation of reactive oxygen species. Probably involved in the extracytoplasmic stress response | ||
BNJPHLCL_00669 | 3e-27 | |||||
BNJPHLCL_00670 | 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 | |
BNJPHLCL_00671 | 2.3e-240 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
BNJPHLCL_00673 | 1.8e-76 | |||||
BNJPHLCL_00674 | 5.6e-207 | NU | Pilus assembly protein PilX | |||
BNJPHLCL_00675 | 1.6e-142 | XK27_04815 | S | Membrane transport protein | ||
BNJPHLCL_00676 | 3.5e-304 | yhcX | K | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | ||
BNJPHLCL_00677 | 7e-23 | S | Uncharacterized small protein (DUF2292) | |||
BNJPHLCL_00678 | 6e-94 | ssuE | 1.5.1.38 | S | FMN reductase | |
BNJPHLCL_00679 | 8e-137 | ssuB | P | Part of the ABC transporter complex SsuABC involved in aliphatic sulfonates import. Responsible for energy coupling to the transport system | ||
BNJPHLCL_00680 | 9.9e-135 | ssuC | P | COG0600 ABC-type nitrate sulfonate bicarbonate transport system, permease component | ||
BNJPHLCL_00681 | 2.1e-213 | ssuD | 1.14.14.5 | C | Catalyzes the desulfonation of aliphatic sulfonates | |
BNJPHLCL_00682 | 1.7e-163 | P | ABC transporter substrate-binding protein | |||
BNJPHLCL_00683 | 8.5e-187 | 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 | |
BNJPHLCL_00684 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
BNJPHLCL_00685 | 4e-71 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
BNJPHLCL_00686 | 5e-111 | 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 | |
BNJPHLCL_00687 | 4.2e-234 | pdp | 2.4.2.2, 2.4.2.4 | F | phosphorylase | |
BNJPHLCL_00688 | 4.3e-233 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
BNJPHLCL_00689 | 1.1e-172 | deoR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
BNJPHLCL_00690 | 4.9e-128 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
BNJPHLCL_00691 | 1.9e-209 | nupG | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
BNJPHLCL_00692 | 6.2e-225 | pbuO_1 | S | permease | ||
BNJPHLCL_00693 | 1.6e-117 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
BNJPHLCL_00694 | 3e-165 | S | Protein of unknown function (DUF979) | |||
BNJPHLCL_00695 | 8.5e-117 | S | Protein of unknown function (DUF969) | |||
BNJPHLCL_00696 | 7.4e-138 | ycsF | S | Belongs to the UPF0271 (lamB) family | ||
BNJPHLCL_00697 | 1.4e-184 | kipA | 6.3.4.6 | E | Allophanate hydrolase subunit 2 | |
BNJPHLCL_00698 | 5.1e-133 | kipI | 3.5.1.54 | E | Allophanate hydrolase subunit 1 | |
BNJPHLCL_00699 | 1.1e-212 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_00700 | 1.1e-77 | ymaD | O | redox protein, regulator of disulfide bond formation | ||
BNJPHLCL_00701 | 5e-128 | artM | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
BNJPHLCL_00702 | 6.4e-114 | artQ | E | COG0765 ABC-type amino acid transport system, permease component | ||
BNJPHLCL_00703 | 2e-130 | artP | ET | COG0834 ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
BNJPHLCL_00704 | 3.3e-206 | hipO3 | 3.5.1.47 | S | amidohydrolase | |
BNJPHLCL_00705 | 0.0 | htpG | O | Molecular chaperone. Has ATPase activity | ||
BNJPHLCL_00706 | 5.7e-184 | M | FFAT motif binding | |||
BNJPHLCL_00707 | 1.4e-56 | I | Domain of unknown function (DUF4430) | |||
BNJPHLCL_00708 | 1.9e-90 | S | Psort location CytoplasmicMembrane, score | |||
BNJPHLCL_00709 | 4.5e-114 | crtF | 2.1.1.210, 2.1.1.281, 2.1.1.79 | M | Methyltransferase | |
BNJPHLCL_00710 | 4.3e-211 | yurR | 1.4.5.1 | E | COG0665 Glycine D-amino acid oxidases (deaminating) | |
BNJPHLCL_00711 | 2.5e-30 | S | Nucleotidyltransferase domain | |||
BNJPHLCL_00712 | 1e-190 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
BNJPHLCL_00714 | 1.1e-123 | S | LXG domain of WXG superfamily | |||
BNJPHLCL_00715 | 3.3e-54 | S | LXG domain of WXG superfamily | |||
BNJPHLCL_00718 | 3.8e-140 | S | Protein of unknown function | |||
BNJPHLCL_00720 | 3.8e-145 | pdaC | 3.5.1.104 | G | Polysaccharide deacetylase | |
BNJPHLCL_00721 | 1.5e-63 | M1-1017 | S | Protein of unknown function (DUF1129) | ||
BNJPHLCL_00722 | 1.8e-56 | K | Transcriptional regulator | |||
BNJPHLCL_00723 | 2.3e-11 | S | NADPH-dependent FMN reductase | |||
BNJPHLCL_00724 | 1.3e-127 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
BNJPHLCL_00725 | 1.5e-177 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
BNJPHLCL_00726 | 2.3e-101 | yieF | S | NAD(P)H-dependent FMN reductase | ||
BNJPHLCL_00727 | 4.3e-97 | ypdE | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
BNJPHLCL_00728 | 9.6e-80 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
BNJPHLCL_00730 | 3.3e-56 | 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 | ||
BNJPHLCL_00731 | 3.4e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
BNJPHLCL_00732 | 1e-103 | 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 | ||
BNJPHLCL_00733 | 4.5e-220 | G | Transmembrane secretion effector | |||
BNJPHLCL_00734 | 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) | |
BNJPHLCL_00735 | 8.3e-151 | ytxC | S | YtxC-like family | ||
BNJPHLCL_00736 | 8.4e-176 | dnaI | L | Primosomal protein DnaI | ||
BNJPHLCL_00737 | 2.1e-260 | dnaB | L | Membrane attachment protein | ||
BNJPHLCL_00738 | 2.1e-79 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
BNJPHLCL_00739 | 3.2e-86 | 2.3.1.178 | J | Benzoate transporter | ||
BNJPHLCL_00740 | 1.2e-191 | gapB | 1.2.1.12, 1.2.1.59 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BNJPHLCL_00741 | 3.6e-103 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
BNJPHLCL_00742 | 2.4e-105 | ytaF | P | Probably functions as a manganese efflux pump | ||
BNJPHLCL_00743 | 8.5e-156 | 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 | |
BNJPHLCL_00744 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
BNJPHLCL_00745 | 1.6e-19 | ydjE | EGP | Major facilitator superfamily | ||
BNJPHLCL_00746 | 4.2e-74 | K | transcriptional | |||
BNJPHLCL_00747 | 3e-210 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_00748 | 1.7e-179 | K | Transcriptional regulator | |||
BNJPHLCL_00750 | 0.0 | bga2 | 3.2.1.23 | G | beta-galactosidase | |
BNJPHLCL_00752 | 2e-110 | opuCD | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
BNJPHLCL_00753 | 1e-170 | opuCC | M | COG1732 Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BNJPHLCL_00754 | 3.4e-115 | opuCB | P | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
BNJPHLCL_00755 | 4.4e-211 | opuCA | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
BNJPHLCL_00756 | 8.5e-96 | yvbF | K | Belongs to the GbsR family | ||
BNJPHLCL_00757 | 1e-96 | maa | 2.3.1.79 | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | |
BNJPHLCL_00758 | 2.1e-37 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BNJPHLCL_00759 | 6.9e-136 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BNJPHLCL_00760 | 3.2e-46 | |||||
BNJPHLCL_00761 | 2.6e-111 | yjlB | S | Cupin domain | ||
BNJPHLCL_00762 | 6.9e-150 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
BNJPHLCL_00763 | 6.5e-136 | yflN_1 | S | Metallo-beta-lactamase superfamily | ||
BNJPHLCL_00764 | 4.7e-51 | pnbA | CE10 | I | Belongs to the type-B carboxylesterase lipase family | |
BNJPHLCL_00765 | 5.7e-302 | comM | O | Mg chelatase subunit ChlI | ||
BNJPHLCL_00766 | 4.1e-149 | S | transposase or invertase | |||
BNJPHLCL_00767 | 4.6e-21 | |||||
BNJPHLCL_00768 | 3.9e-201 | gldA | 1.1.1.1, 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
BNJPHLCL_00769 | 4.4e-208 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
BNJPHLCL_00770 | 3.2e-158 | nadC | 1.4.3.16, 2.4.2.19 | H | Belongs to the NadC ModD family | |
BNJPHLCL_00771 | 2.1e-304 | nadB | 1.3.5.4, 1.4.3.16 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
BNJPHLCL_00772 | 8e-205 | nifS | 2.8.1.7 | E | Cysteine desulfurase | |
BNJPHLCL_00773 | 5.4e-144 | L | Transposase DDE domain | |||
BNJPHLCL_00774 | 7e-220 | dapL | 2.6.1.83 | E | Aminotransferase | |
BNJPHLCL_00775 | 9.2e-264 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
BNJPHLCL_00776 | 4.8e-232 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
BNJPHLCL_00777 | 2.6e-177 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
BNJPHLCL_00778 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase ammonia chain | |
BNJPHLCL_00779 | 1.5e-205 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
BNJPHLCL_00780 | 1.1e-223 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
BNJPHLCL_00781 | 4.3e-141 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
BNJPHLCL_00782 | 6.8e-234 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
BNJPHLCL_00783 | 2e-199 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
BNJPHLCL_00785 | 9.7e-77 | |||||
BNJPHLCL_00786 | 2.5e-36 | P | catalase activity | |||
BNJPHLCL_00787 | 1.6e-79 | |||||
BNJPHLCL_00788 | 2.3e-30 | cspD | K | Cold shock | ||
BNJPHLCL_00790 | 6.7e-170 | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | ||
BNJPHLCL_00791 | 6.6e-276 | dacC | 3.4.16.4 | M | D-alanyl-D-alanine carboxypeptidase | |
BNJPHLCL_00792 | 4.4e-106 | plsC | 2.3.1.51 | I | Belongs to the 1-acyl-sn-glycerol-3-phosphate acyltransferase family | |
BNJPHLCL_00793 | 5.6e-77 | yneK | S | Protein of unknown function (DUF2621) | ||
BNJPHLCL_00794 | 4.6e-77 | yneJ | O | COG4846 Membrane protein involved in cytochrome C biogenesis | ||
BNJPHLCL_00795 | 1.6e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | cheY-homologous receiver domain | |
BNJPHLCL_00796 | 6.4e-128 | ccdA | O | cytochrome c biogenesis protein | ||
BNJPHLCL_00797 | 6.8e-28 | yneF | S | UPF0154 protein | ||
BNJPHLCL_00798 | 5.3e-72 | yneE | S | Sporulation inhibitor of replication protein sirA | ||
BNJPHLCL_00799 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
BNJPHLCL_00800 | 3.4e-33 | ynzC | S | UPF0291 protein | ||
BNJPHLCL_00801 | 5.2e-116 | yneB | L | resolvase | ||
BNJPHLCL_00802 | 8e-52 | yneA | D | Inhibits cell division during the SOS response. Affects a later stage of the cell division protein assembly, after the assembly of the Z ring, by probably suppressing recruitment of FtsL and or DivIC to the division machinery | ||
BNJPHLCL_00803 | 1.2e-109 | 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 | |
BNJPHLCL_00804 | 6.4e-262 | glnA | 6.3.1.2 | E | glutamine synthetase | |
BNJPHLCL_00805 | 3e-63 | glnR | K | transcriptional | ||
BNJPHLCL_00806 | 0.0 | S | Dynamin family | |||
BNJPHLCL_00807 | 5e-33 | |||||
BNJPHLCL_00808 | 2.4e-142 | f42a | O | prohibitin homologues | ||
BNJPHLCL_00809 | 3e-232 | pbuX | F | xanthine | ||
BNJPHLCL_00810 | 1.6e-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 | |
BNJPHLCL_00811 | 9.7e-299 | ypwA | 3.4.17.19 | E | Broad specificity carboxypetidase that releases amino acids sequentially from the C-terminus, including neutral, aromatic, polar and basic residues | |
BNJPHLCL_00812 | 2.2e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
BNJPHLCL_00813 | 3.4e-46 | 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 | ||
BNJPHLCL_00814 | 3.4e-100 | ypsA | S | Belongs to the UPF0398 family | ||
BNJPHLCL_00815 | 5.4e-45 | cotD | S | Inner spore coat protein D | ||
BNJPHLCL_00816 | 1.1e-253 | yprB | L | RNase_H superfamily | ||
BNJPHLCL_00817 | 0.0 | yprA | L | COG1205 Distinct helicase family with a unique C-terminal domain including a metal-binding cysteine cluster | ||
BNJPHLCL_00818 | 2e-74 | hspX | O | Belongs to the small heat shock protein (HSP20) family | ||
BNJPHLCL_00820 | 9.5e-62 | yppG | S | YppG-like protein | ||
BNJPHLCL_00821 | 1.1e-62 | yppE | S | Bacterial domain of unknown function (DUF1798) | ||
BNJPHLCL_00824 | 1.1e-112 | 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 | ||
BNJPHLCL_00825 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BNJPHLCL_00826 | 5.4e-121 | 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 | |
BNJPHLCL_00827 | 2.8e-128 | dnaD | L | DNA replication protein DnaD | ||
BNJPHLCL_00828 | 2e-260 | asnS | 6.1.1.22 | J | asparaginyl-tRNA | |
BNJPHLCL_00829 | 9.5e-217 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
BNJPHLCL_00830 | 1.3e-76 | ypmB | S | protein conserved in bacteria | ||
BNJPHLCL_00831 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
BNJPHLCL_00832 | 7.9e-64 | panD | 4.1.1.11 | H | Catalyzes the pyruvoyl-dependent decarboxylation of aspartate to produce beta-alanine | |
BNJPHLCL_00833 | 5.9e-160 | panC | 2.7.4.25, 6.3.2.1 | H | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate | |
BNJPHLCL_00834 | 7.1e-150 | panB | 2.1.2.11 | H | Catalyzes the reversible reaction in which hydroxymethyl group from 5,10-methylenetetrahydrofolate is transferred onto alpha-ketoisovalerate to form ketopantoate | |
BNJPHLCL_00835 | 2.9e-171 | birA | 6.3.4.15 | K | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
BNJPHLCL_00836 | 1.9e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
BNJPHLCL_00837 | 8.8e-215 | bshA | GT4 | M | N-acetyl-alpha-D-glucosaminyl L-malate synthase | |
BNJPHLCL_00838 | 6.2e-131 | bshB1 | S | proteins, LmbE homologs | ||
BNJPHLCL_00839 | 2.8e-148 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
BNJPHLCL_00840 | 1.7e-57 | ypjD | 2.5.1.19 | S | Nucleotide pyrophosphohydrolase | |
BNJPHLCL_00841 | 2.4e-161 | ypjC | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
BNJPHLCL_00842 | 3.1e-81 | queT | S | QueT transporter | ||
BNJPHLCL_00843 | 3.4e-102 | yugP | S | Zn-dependent protease | ||
BNJPHLCL_00844 | 6e-143 | ypjB | S | sporulation protein | ||
BNJPHLCL_00845 | 1.6e-108 | ypjA | S | membrane | ||
BNJPHLCL_00846 | 1.6e-145 | qcrC | C | Menaquinol-cytochrome c reductase cytochrome b c subunit | ||
BNJPHLCL_00847 | 1.2e-126 | petB | C | COG1290 Cytochrome b subunit of the bc complex | ||
BNJPHLCL_00848 | 1.3e-98 | qcrA | C | Menaquinol-cytochrome c reductase | ||
BNJPHLCL_00849 | 1.9e-80 | ypiF | S | Protein of unknown function (DUF2487) | ||
BNJPHLCL_00850 | 5.9e-97 | ypiB | S | Belongs to the UPF0302 family | ||
BNJPHLCL_00851 | 1.9e-239 | S | COG0457 FOG TPR repeat | |||
BNJPHLCL_00852 | 6.7e-232 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
BNJPHLCL_00853 | 9.4e-203 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
BNJPHLCL_00854 | 7.9e-210 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
BNJPHLCL_00855 | 3.8e-60 | aroH | 2.7.4.25, 5.4.99.5 | E | Catalyzes the Claisen rearrangement of chorismate to prephenate. Probably involved in the aromatic amino acid biosynthesis | |
BNJPHLCL_00856 | 4.4e-205 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
BNJPHLCL_00857 | 1.1e-220 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
BNJPHLCL_00858 | 2.4e-144 | cheR | 2.1.1.80 | NT | COG1352 Methylase of chemotaxis methyl-accepting proteins | |
BNJPHLCL_00859 | 7.2e-77 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
BNJPHLCL_00860 | 1.9e-170 | hepT | 2.5.1.30, 2.5.1.83, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
BNJPHLCL_00861 | 6.4e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
BNJPHLCL_00862 | 3.3e-144 | hepS | 2.5.1.30 | H | Heptaprenyl diphosphate synthase (HEPPP synthase) subunit 1 | |
BNJPHLCL_00863 | 8.7e-34 | mtrB | K | Required for transcription attenuation control in the Trp operon. This trans-acting factor seems to recognize a 10 bases nucleotide sequence in the Trp leader transcript causing transcription termination. Binds the leader RNA only in presence of L-tryptophan | ||
BNJPHLCL_00864 | 3.9e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
BNJPHLCL_00865 | 8.3e-279 | spoIVA | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | ||
BNJPHLCL_00866 | 1.7e-136 | yphF | ||||
BNJPHLCL_00867 | 3.2e-08 | yphE | S | Protein of unknown function (DUF2768) | ||
BNJPHLCL_00868 | 1.6e-191 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
BNJPHLCL_00869 | 5.5e-250 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
BNJPHLCL_00870 | 2.4e-19 | yphA | ||||
BNJPHLCL_00871 | 7.3e-14 | S | YpzI-like protein | |||
BNJPHLCL_00872 | 9.4e-206 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
BNJPHLCL_00873 | 1.1e-119 | 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 | |
BNJPHLCL_00874 | 8.7e-116 | ypfA | M | Flagellar protein YcgR | ||
BNJPHLCL_00875 | 2.9e-254 | hemX | 2.1.1.107, 4.2.1.75 | H | sporulation protein | |
BNJPHLCL_00876 | 1e-145 | sleB | 3.5.1.28 | M | Spore cortex-lytic enzyme | |
BNJPHLCL_00877 | 1.2e-123 | prsW | S | Involved in the degradation of specific anti-sigma factors | ||
BNJPHLCL_00878 | 3e-184 | ypdA | 1.18.1.2, 1.19.1.1, 1.8.1.9 | O | COG0492 Thioredoxin reductase | |
BNJPHLCL_00879 | 4.4e-244 | gudB | 1.4.1.2, 1.4.1.3 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
BNJPHLCL_00880 | 3.8e-96 | mecB | NOT | Negative regulator of genetic competence (MecA) | ||
BNJPHLCL_00881 | 1.8e-144 | ypbG | S | Calcineurin-like phosphoesterase superfamily domain | ||
BNJPHLCL_00882 | 2.6e-30 | cotJA | S | Spore coat associated protein JA (CotJA) | ||
BNJPHLCL_00883 | 1.2e-44 | cotJB | S | CotJB protein | ||
BNJPHLCL_00884 | 1.5e-103 | cotJC | P | Spore Coat | ||
BNJPHLCL_00885 | 1.2e-79 | ypbF | S | Protein of unknown function (DUF2663) | ||
BNJPHLCL_00887 | 1.2e-100 | ypbD | S | metal-dependent membrane protease | ||
BNJPHLCL_00888 | 8.3e-279 | recQ | 3.6.4.12 | L | DNA helicase | |
BNJPHLCL_00889 | 1.1e-203 | ypbB | 5.1.3.1 | S | protein conserved in bacteria | |
BNJPHLCL_00890 | 8.8e-136 | IQ | Short-chain dehydrogenase reductase sdr | |||
BNJPHLCL_00891 | 4e-36 | 2.4.1.21 | GT4,GT5 | G | Glycosyl transferase 4-like | |
BNJPHLCL_00892 | 5.8e-89 | cpsE | M | Bacterial sugar transferase | ||
BNJPHLCL_00893 | 8.9e-159 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
BNJPHLCL_00894 | 1.2e-140 | ywqE | 3.1.3.48 | GM | COG4464 Capsular polysaccharide biosynthesis protein | |
BNJPHLCL_00895 | 1.2e-111 | ywqD | 2.7.10.1 | D | COG0489 ATPases involved in chromosome partitioning | |
BNJPHLCL_00896 | 1.5e-119 | ywqC | M | biosynthesis protein | ||
BNJPHLCL_00897 | 2.5e-144 | E | lipolytic protein G-D-S-L family | |||
BNJPHLCL_00898 | 3.2e-96 | sigS | 2.7.7.6 | K | Belongs to the sigma-70 factor family. ECF subfamily | |
BNJPHLCL_00899 | 1.5e-88 | K | ComK protein | |||
BNJPHLCL_00901 | 1.6e-09 | csbD | S | Belongs to the UPF0337 (CsbD) family | ||
BNJPHLCL_00903 | 0.0 | metH | 2.1.1.13 | E | Methionine synthase | |
BNJPHLCL_00904 | 0.0 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | Catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
BNJPHLCL_00905 | 6e-153 | msrR | K | COG1316 Transcriptional regulator | ||
BNJPHLCL_00906 | 5.3e-99 | yngC | S | membrane-associated protein | ||
BNJPHLCL_00907 | 5.7e-228 | S | SNARE associated Golgi protein | |||
BNJPHLCL_00908 | 2.4e-53 | yodB | K | transcriptional | ||
BNJPHLCL_00909 | 4.6e-194 | S | Protein of unknown function (DUF1648) | |||
BNJPHLCL_00910 | 1.3e-69 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
BNJPHLCL_00911 | 9.6e-116 | glnP | P | ABC transporter | ||
BNJPHLCL_00912 | 4e-108 | gluC | P | ABC transporter | ||
BNJPHLCL_00913 | 1.2e-135 | glnH | ET | Belongs to the bacterial solute-binding protein 3 family | ||
BNJPHLCL_00914 | 4.9e-131 | glnQ | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
BNJPHLCL_00915 | 1.1e-173 | ydbI | S | AI-2E family transporter | ||
BNJPHLCL_00916 | 3e-24 | tatA | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes. TatA could form the protein-conducting channel of the Tat system | ||
BNJPHLCL_00917 | 1.4e-145 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
BNJPHLCL_00918 | 0.0 | ydaO | E | amino acid | ||
BNJPHLCL_00920 | 2.3e-278 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
BNJPHLCL_00922 | 2.3e-187 | T | HD domain | |||
BNJPHLCL_00924 | 1.1e-214 | yqiG | C | COG1902 NADH flavin oxidoreductases, Old Yellow Enzyme family | ||
BNJPHLCL_00925 | 2.6e-89 | S | Belongs to the UPF0312 family | |||
BNJPHLCL_00926 | 1.6e-123 | ric | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | ||
BNJPHLCL_00927 | 7.8e-145 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
BNJPHLCL_00928 | 2.1e-41 | fdxA | C | 4Fe-4S binding domain | ||
BNJPHLCL_00929 | 3.8e-168 | yclQ | P | COG4607 ABC-type enterochelin transport system, periplasmic component | ||
BNJPHLCL_00930 | 6.2e-137 | yclP | 3.6.3.34 | P | ABC transporter, ATP-binding protein | |
BNJPHLCL_00931 | 4.1e-162 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
BNJPHLCL_00932 | 3.9e-165 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
BNJPHLCL_00933 | 1.1e-220 | minJ | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | ||
BNJPHLCL_00934 | 3.5e-266 | ctpB | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
BNJPHLCL_00935 | 2.8e-182 | 1.1.1.3 | E | homoserine dehydrogenase | ||
BNJPHLCL_00936 | 4.3e-247 | metY | 2.5.1.49 | E | O-acetylhomoserine | |
BNJPHLCL_00937 | 6.2e-271 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
BNJPHLCL_00938 | 5.5e-96 | D | peptidase | |||
BNJPHLCL_00939 | 4.5e-155 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
BNJPHLCL_00940 | 9.3e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
BNJPHLCL_00941 | 5.5e-50 | cccB | C | COG2010 Cytochrome c, mono- and diheme variants | ||
BNJPHLCL_00942 | 4.7e-157 | yvjA | S | Uncharacterized protein conserved in bacteria (DUF2179) | ||
BNJPHLCL_00943 | 2.3e-168 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
BNJPHLCL_00944 | 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 | ||
BNJPHLCL_00945 | 8.2e-145 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
BNJPHLCL_00946 | 8.7e-08 | S | YqzL-like protein | |||
BNJPHLCL_00947 | 5.6e-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 | ||
BNJPHLCL_00948 | 7.9e-67 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
BNJPHLCL_00949 | 4.2e-83 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
BNJPHLCL_00950 | 2e-163 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
BNJPHLCL_00951 | 5.4e-55 | yqfF | S | membrane-associated HD superfamily hydrolase | ||
BNJPHLCL_00952 | 6.1e-174 | phoH | T | Phosphate starvation-inducible protein PhoH | ||
BNJPHLCL_00953 | 3.6e-224 | yqfD | 3.1.3.102, 3.1.3.104 | S | Stage IV sporulation | |
BNJPHLCL_00954 | 3.2e-46 | yqfC | S | sporulation protein YqfC | ||
BNJPHLCL_00955 | 6.6e-70 | yqeY | S | Yqey-like protein | ||
BNJPHLCL_00956 | 1.2e-19 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
BNJPHLCL_00957 | 2.2e-47 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
BNJPHLCL_00958 | 4.3e-156 | yqeW | P | COG1283 Na phosphate symporter | ||
BNJPHLCL_00959 | 1.2e-260 | yqeV | 2.8.4.5 | J | ribosomal protein S12 methylthiotransferase | |
BNJPHLCL_00960 | 2.7e-140 | 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 | |
BNJPHLCL_00961 | 1.9e-172 | prmA | J | Methylates ribosomal protein L11 | ||
BNJPHLCL_00962 | 1.6e-205 | 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 | ||
BNJPHLCL_00963 | 3.6e-308 | dnaK | O | Heat shock 70 kDa protein | ||
BNJPHLCL_00964 | 1.4e-89 | 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 | ||
BNJPHLCL_00965 | 8.3e-185 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
BNJPHLCL_00966 | 3.7e-218 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
BNJPHLCL_00967 | 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 | ||
BNJPHLCL_00968 | 2.9e-221 | spoIIP | M | stage II sporulation protein P | ||
BNJPHLCL_00969 | 4.7e-202 | gpr | 3.4.24.78 | C | Initiates the rapid degradation of small, acid-soluble proteins during spore germination | |
BNJPHLCL_00970 | 2.9e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
BNJPHLCL_00971 | 1e-187 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
BNJPHLCL_00973 | 0.0 | comEC | S | Competence protein ComEC | ||
BNJPHLCL_00974 | 2.1e-111 | comEB | 3.5.4.12 | F | COG2131 Deoxycytidylate deaminase | |
BNJPHLCL_00975 | 8.8e-93 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
BNJPHLCL_00976 | 1.1e-147 | comER | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | ||
BNJPHLCL_00977 | 2.5e-146 | cmoA | S | Methyltransferase domain | ||
BNJPHLCL_00978 | 1.1e-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 | ||
BNJPHLCL_00979 | 3.4e-103 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
BNJPHLCL_00980 | 5e-107 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
BNJPHLCL_00981 | 3.6e-45 | yhbY | J | RNA-binding protein containing KH domain, possibly ribosomal protein | ||
BNJPHLCL_00982 | 4e-161 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
BNJPHLCL_00983 | 2e-213 | yqeH | S | In Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
BNJPHLCL_00984 | 9.9e-94 | yqeG | S | hydrolase of the HAD superfamily | ||
BNJPHLCL_00985 | 2.8e-257 | glcF | C | Glycolate oxidase | ||
BNJPHLCL_00986 | 7.7e-258 | glcD | 1.1.3.15 | C | Glycolate oxidase subunit | |
BNJPHLCL_00987 | 1.6e-205 | ysfB | KT | regulator | ||
BNJPHLCL_00988 | 4.3e-224 | mco | 1.16.3.3 | Q | multicopper oxidases | |
BNJPHLCL_00989 | 9.6e-74 | hsp18 | O | Belongs to the small heat shock protein (HSP20) family | ||
BNJPHLCL_00990 | 7.8e-22 | S | Short C-terminal domain | |||
BNJPHLCL_00991 | 2.1e-103 | CO | alkyl hydroperoxide reductase Thiol specific antioxidant Mal allergen | |||
BNJPHLCL_00992 | 1.3e-116 | S | TPM domain | |||
BNJPHLCL_00993 | 6.5e-78 | lemA | S | LemA family | ||
BNJPHLCL_00994 | 4.3e-59 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BNJPHLCL_00995 | 1.2e-57 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BNJPHLCL_00996 | 9.1e-119 | S | VIT family | |||
BNJPHLCL_00997 | 5.1e-154 | czcD | P | COG1230 Co Zn Cd efflux system component | ||
BNJPHLCL_00998 | 2.7e-14 | sda | S | Sporulation inhibitor A | ||
BNJPHLCL_00999 | 4.8e-91 | pssA | 2.7.8.8 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
BNJPHLCL_01000 | 6.1e-126 | sigK | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
BNJPHLCL_01001 | 6.2e-293 | ahpF | O | Alkyl hydroperoxide reductase | ||
BNJPHLCL_01002 | 3.8e-107 | ahpC | 1.11.1.15 | O | Alkyl hydroperoxide reductase | |
BNJPHLCL_01004 | 1.7e-10 | S | YrhC-like protein | |||
BNJPHLCL_01005 | 4.6e-123 | 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 | |
BNJPHLCL_01006 | 6.4e-28 | yrzA | S | Protein of unknown function (DUF2536) | ||
BNJPHLCL_01007 | 7.9e-58 | yrrS | S | Protein of unknown function (DUF1510) | ||
BNJPHLCL_01008 | 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 | ||
BNJPHLCL_01009 | 1.7e-111 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
BNJPHLCL_01010 | 7.4e-115 | yrrM | 2.1.1.104 | S | O-methyltransferase | |
BNJPHLCL_01011 | 1.5e-203 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
BNJPHLCL_01012 | 1.5e-41 | yrzB | S | Belongs to the UPF0473 family | ||
BNJPHLCL_01013 | 6.8e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
BNJPHLCL_01014 | 2.2e-44 | yrzL | S | Belongs to the UPF0297 family | ||
BNJPHLCL_01015 | 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 | |
BNJPHLCL_01016 | 3.8e-172 | yrrI | S | AI-2E family transporter | ||
BNJPHLCL_01018 | 4e-29 | yrzR | ||||
BNJPHLCL_01019 | 8.2e-73 | yndM | S | Protein of unknown function (DUF2512) | ||
BNJPHLCL_01020 | 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 | |
BNJPHLCL_01021 | 1.3e-125 | S | COG0457 FOG TPR repeat | |||
BNJPHLCL_01022 | 9.8e-224 | 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 | |
BNJPHLCL_01023 | 2.6e-208 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
BNJPHLCL_01024 | 2.3e-72 | cymR | K | Transcriptional regulator | ||
BNJPHLCL_01025 | 4.3e-71 | K | Transcriptional | |||
BNJPHLCL_01026 | 4.9e-116 | cobC | 3.1.3.3, 3.1.3.73, 5.4.2.12 | G | Histidine phosphatase superfamily (branch 1) | |
BNJPHLCL_01027 | 2.1e-225 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
BNJPHLCL_01028 | 2.5e-222 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
BNJPHLCL_01029 | 5.3e-153 | K | RpiR family transcriptional regulator | |||
BNJPHLCL_01030 | 2.8e-144 | ypuA | S | Secreted protein | ||
BNJPHLCL_01031 | 2e-105 | |||||
BNJPHLCL_01032 | 2.6e-68 | S | response to pH | |||
BNJPHLCL_01033 | 1.3e-105 | che | ||||
BNJPHLCL_01034 | 1.2e-293 | K | helix_turn_helix, Lux Regulon | |||
BNJPHLCL_01036 | 2e-89 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
BNJPHLCL_01037 | 1.1e-21 | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | ||
BNJPHLCL_01038 | 2.8e-102 | 4.2.1.1 | P | Reversible hydration of carbon dioxide | ||
BNJPHLCL_01039 | 1.9e-115 | yrrT | 4.4.1.21 | Q | Could be a S-adenosyl-L-methionine-dependent methyltransferase | |
BNJPHLCL_01040 | 1.4e-86 | luxS | 4.4.1.21 | T | 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) | |
BNJPHLCL_01041 | 5.7e-169 | mccA | 2.5.1.134, 2.5.1.47 | E | Cysteine synthase | |
BNJPHLCL_01042 | 1.9e-211 | mccB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
BNJPHLCL_01043 | 3.6e-89 | yuaF | OU | Membrane protein implicated in regulation of membrane protease activity | ||
BNJPHLCL_01044 | 1.7e-170 | yuaG | S | protein conserved in bacteria | ||
BNJPHLCL_01045 | 2.6e-183 | mreB | D | Rod-share determining protein MreBH | ||
BNJPHLCL_01046 | 5.8e-86 | ykhA | 3.1.2.20 | I | Acyl-CoA hydrolase | |
BNJPHLCL_01047 | 1.5e-146 | dksA | T | COG1734 DnaK suppressor protein | ||
BNJPHLCL_01048 | 1.5e-228 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_01049 | 3.7e-60 | yeaO | S | Protein of unknown function, DUF488 | ||
BNJPHLCL_01051 | 2e-60 | yhdN | S | Domain of unknown function (DUF1992) | ||
BNJPHLCL_01052 | 6.6e-137 | motA | N | flagellar motor | ||
BNJPHLCL_01053 | 4.2e-139 | motB | N | Flagellar motor protein | ||
BNJPHLCL_01054 | 9.7e-141 | |||||
BNJPHLCL_01055 | 2.9e-241 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BNJPHLCL_01056 | 8.1e-267 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
BNJPHLCL_01057 | 9.3e-172 | yegS | 2.7.1.107 | I | COG1597 Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
BNJPHLCL_01058 | 2e-146 | Q | N-acetyltransferase | |||
BNJPHLCL_01061 | 3.3e-272 | 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) | |
BNJPHLCL_01062 | 1.6e-274 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
BNJPHLCL_01063 | 4.3e-46 | 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) | |
BNJPHLCL_01064 | 1.4e-245 | aceA | 4.1.3.1 | C | Isocitrate lyase | |
BNJPHLCL_01065 | 0.0 | aceB | 2.3.3.9 | C | Belongs to the malate synthase family | |
BNJPHLCL_01066 | 2.7e-216 | camS | S | COG4851 Protein involved in sex pheromone biosynthesis | ||
BNJPHLCL_01067 | 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 | |
BNJPHLCL_01068 | 1.2e-283 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
BNJPHLCL_01069 | 3.2e-211 | L | RNA-directed DNA polymerase (reverse transcriptase) | |||
BNJPHLCL_01070 | 7.7e-126 | pcrA | 3.6.4.12 | L | AAA domain | |
BNJPHLCL_01071 | 1.4e-127 | pcrB | I | 35 carbon atoms) to the C3 hydroxyl of sn-glycerol-1-phosphate (G1P), producing heptaprenylglyceryl phosphate (HepGP). This reaction is an ether-bond-formation step in the biosynthesis of archaea-type G1P-based membrane lipids found in Bacillales | ||
BNJPHLCL_01072 | 2.2e-54 | yerC | S | protein conserved in bacteria | ||
BNJPHLCL_01073 | 4.2e-189 | yerB | S | Protein of unknown function (DUF3048) C-terminal domain | ||
BNJPHLCL_01074 | 0.0 | yerA | 3.5.4.2 | F | adenine deaminase | |
BNJPHLCL_01075 | 3.2e-36 | S | Protein of unknown function (DUF2892) | |||
BNJPHLCL_01076 | 3.5e-230 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
BNJPHLCL_01077 | 2e-288 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
BNJPHLCL_01078 | 4.1e-104 | 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 | |
BNJPHLCL_01079 | 1.3e-190 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
BNJPHLCL_01080 | 4.2e-272 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
BNJPHLCL_01081 | 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 | |
BNJPHLCL_01082 | 3.8e-125 | 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 | |
BNJPHLCL_01083 | 7.1e-37 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
BNJPHLCL_01084 | 3.9e-125 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
BNJPHLCL_01085 | 4.3e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
BNJPHLCL_01086 | 4.6e-216 | 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) | |
BNJPHLCL_01087 | 3.4e-83 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
BNJPHLCL_01088 | 1.1e-30 | yebG | S | NETI protein | ||
BNJPHLCL_01089 | 2.4e-90 | yebE | S | UPF0316 protein | ||
BNJPHLCL_01090 | 1.7e-131 | frnE | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
BNJPHLCL_01091 | 8.1e-276 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BNJPHLCL_01092 | 2.9e-51 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BNJPHLCL_01093 | 0.0 | rafA | 3.2.1.22 | G | Alpha-galactosidase | |
BNJPHLCL_01094 | 1.5e-109 | proA_2 | H | Methyltransferase | ||
BNJPHLCL_01095 | 1.4e-225 | yhdR | 2.6.1.1 | E | Aminotransferase | |
BNJPHLCL_01096 | 5.7e-112 | yhbD | K | Protein of unknown function (DUF4004) | ||
BNJPHLCL_01098 | 5.7e-245 | yeeO | V | Mate efflux family protein | ||
BNJPHLCL_01099 | 8.1e-157 | mmgB | 1.1.1.157 | I | Dehydrogenase | |
BNJPHLCL_01101 | 0.0 | L | AAA domain | |||
BNJPHLCL_01102 | 2.7e-241 | yhaO | L | Calcineurin-like phosphoesterase superfamily domain | ||
BNJPHLCL_01103 | 1.2e-29 | K | sequence-specific DNA binding | |||
BNJPHLCL_01104 | 6.6e-127 | yflK | S | protein conserved in bacteria | ||
BNJPHLCL_01105 | 2.5e-08 | ykyB | S | YkyB-like protein | ||
BNJPHLCL_01106 | 1.4e-113 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | 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) | |
BNJPHLCL_01107 | 7e-147 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BNJPHLCL_01108 | 2.7e-122 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
BNJPHLCL_01109 | 1.5e-135 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BNJPHLCL_01110 | 9.5e-98 | 1.5.1.38 | S | FMN reductase | ||
BNJPHLCL_01111 | 7.7e-140 | I | alpha/beta hydrolase fold | |||
BNJPHLCL_01112 | 3.5e-21 | M | Spore coat protein | |||
BNJPHLCL_01113 | 1.1e-146 | yvaK | 3.1.1.1 | S | BAAT / Acyl-CoA thioester hydrolase C terminal | |
BNJPHLCL_01115 | 9.2e-144 | ykrA | S | hydrolases of the HAD superfamily | ||
BNJPHLCL_01116 | 1.3e-62 | hxlB | 4.1.2.43, 5.3.1.27 | M | arabinose-5-phosphate isomerase activity | |
BNJPHLCL_01117 | 4.1e-225 | yfkA | S | YfkB-like domain | ||
BNJPHLCL_01118 | 4e-74 | |||||
BNJPHLCL_01119 | 2.4e-27 | |||||
BNJPHLCL_01120 | 2.1e-70 | yxiE | T | Belongs to the universal stress protein A family | ||
BNJPHLCL_01121 | 3.6e-217 | ykvU | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
BNJPHLCL_01122 | 2.1e-146 | aacC | 2.3.1.81 | V | aminoglycoside | |
BNJPHLCL_01123 | 2.2e-173 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_01124 | 5.1e-25 | S | Protein of unknown function (DUF1657) | |||
BNJPHLCL_01125 | 2.9e-168 | mdh | 1.1.1.37 | C | Catalyzes the reversible oxidation of malate to oxaloacetate | |
BNJPHLCL_01126 | 4e-245 | icd | 1.1.1.42 | C | isocitrate | |
BNJPHLCL_01127 | 4.1e-206 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
BNJPHLCL_01128 | 1e-73 | yeaL | S | Membrane | ||
BNJPHLCL_01129 | 1e-156 | ytvI | S | sporulation integral membrane protein YtvI | ||
BNJPHLCL_01130 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
BNJPHLCL_01131 | 4.1e-178 | 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 | |
BNJPHLCL_01132 | 4.6e-177 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
BNJPHLCL_01133 | 1.1e-164 | 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 | |
BNJPHLCL_01134 | 6.8e-226 | ytsJ | 1.1.1.38 | C | Malate dehydrogenase | |
BNJPHLCL_01135 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BNJPHLCL_01136 | 1.6e-41 | ytrH | S | Sporulation protein YtrH | ||
BNJPHLCL_01137 | 7.9e-88 | ytrI | ||||
BNJPHLCL_01138 | 9.1e-176 | nrnA | 3.1.13.3, 3.1.3.7 | S | COG0618 Exopolyphosphatase-related proteins | |
BNJPHLCL_01139 | 7.1e-39 | ytpI | S | YtpI-like protein | ||
BNJPHLCL_01140 | 2.3e-240 | ytoI | K | transcriptional regulator containing CBS domains | ||
BNJPHLCL_01141 | 1.1e-129 | ytkL | S | Belongs to the UPF0173 family | ||
BNJPHLCL_01142 | 1.6e-178 | pepQ | 3.4.13.9 | E | COG0006 Xaa-Pro aminopeptidase | |
BNJPHLCL_01143 | 7.8e-197 | ald | 1.4.1.1 | E | Belongs to the AlaDH PNT family | |
BNJPHLCL_01144 | 3.1e-78 | uspA | T | Belongs to the universal stress protein A family | ||
BNJPHLCL_01145 | 3.1e-150 | S | EcsC protein family | |||
BNJPHLCL_01146 | 3e-218 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BNJPHLCL_01147 | 2.4e-176 | ytxK | 2.1.1.72 | L | DNA methylase | |
BNJPHLCL_01148 | 2.2e-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 | |
BNJPHLCL_01149 | 2e-66 | ytfJ | S | Sporulation protein YtfJ | ||
BNJPHLCL_01150 | 3.9e-119 | ytfI | S | Protein of unknown function (DUF2953) | ||
BNJPHLCL_01151 | 4.2e-84 | yteJ | S | RDD family | ||
BNJPHLCL_01152 | 6.7e-179 | sppA | OU | signal peptide peptidase SppA | ||
BNJPHLCL_01153 | 2.2e-311 | acsA | 6.2.1.1, 6.2.1.2 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
BNJPHLCL_01154 | 1.4e-27 | sspB | S | spore protein | ||
BNJPHLCL_01155 | 1.9e-225 | 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 | |
BNJPHLCL_01156 | 5.2e-212 | iscS2 | 2.8.1.7 | E | Cysteine desulfurase | |
BNJPHLCL_01157 | 1.6e-302 | 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 | ||
BNJPHLCL_01158 | 1.3e-116 | yttP | K | Transcriptional regulator | ||
BNJPHLCL_01159 | 7e-86 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
BNJPHLCL_01160 | 0.0 | ytrP | 2.7.7.65 | T | COG2199 FOG GGDEF domain | |
BNJPHLCL_01161 | 1.9e-109 | 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 | ||
BNJPHLCL_01162 | 1.3e-145 | |||||
BNJPHLCL_01163 | 2e-126 | |||||
BNJPHLCL_01164 | 5.4e-181 | putA | E | Proline dehydrogenase | ||
BNJPHLCL_01165 | 1.1e-297 | rocA | 1.2.1.88, 1.5.5.2 | C | Belongs to the aldehyde dehydrogenase family. RocA subfamily | |
BNJPHLCL_01166 | 4.5e-255 | prdR | KT | Transcriptional regulator | ||
BNJPHLCL_01167 | 2.2e-240 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
BNJPHLCL_01168 | 3.3e-152 | fdhD | C | Required for formate dehydrogenase (FDH) activity. Acts as a sulfur carrier protein that transfers sulfur from IscS to the molybdenum cofactor prior to its insertion into FDH | ||
BNJPHLCL_01169 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
BNJPHLCL_01170 | 5.7e-89 | yrhD | S | Protein of unknown function (DUF1641) | ||
BNJPHLCL_01171 | 4e-192 | moeB | 2.7.7.80 | H | COG0476 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | |
BNJPHLCL_01172 | 1e-84 | moaC | 4.6.1.17 | H | Catalyzes the conversion of (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate to cyclic pyranopterin monophosphate (cPMP) | |
BNJPHLCL_01173 | 1.1e-33 | moaD | 2.8.1.12 | H | Involved in sulfur transfer in the conversion of molybdopterin precursor Z to molybdopterin | |
BNJPHLCL_01174 | 1.2e-79 | moaE | 2.8.1.12 | H | COG0314 Molybdopterin converting factor, large subunit | |
BNJPHLCL_01175 | 1.6e-85 | mobB | 2.10.1.1, 2.7.7.77 | H | molybdopterin-guanine dinucleotide biosynthesis protein | |
BNJPHLCL_01176 | 1.4e-234 | moeA | 2.10.1.1 | H | molybdopterin | |
BNJPHLCL_01177 | 7.8e-123 | mobA | 2.7.7.77 | H | Transfers a GMP moiety from GTP to Mo-molybdopterin (Mo- MPT) cofactor (Moco or molybdenum cofactor) to form Mo- molybdopterin guanine dinucleotide (Mo-MGD) cofactor | |
BNJPHLCL_01178 | 1.4e-84 | moaB | 2.7.7.75 | H | May be involved in the biosynthesis of molybdopterin | |
BNJPHLCL_01179 | 7.8e-188 | moaA | 4.1.99.22, 4.6.1.17 | H | Catalyzes the cyclization of GTP to (8S)-3',8-cyclo-7,8- dihydroguanosine 5'-triphosphate | |
BNJPHLCL_01180 | 1.5e-129 | modC | 3.6.3.29 | P | ATPases associated with a variety of cellular activities | |
BNJPHLCL_01181 | 6.5e-120 | P | COG4149 ABC-type molybdate transport system, permease component | |||
BNJPHLCL_01182 | 1.5e-133 | modA | P | Molybdenum ABC transporter | ||
BNJPHLCL_01183 | 0.0 | acsA | 6.2.1.1 | I | COG0365 Acyl-coenzyme A synthetases AMP-(fatty) acid ligases | |
BNJPHLCL_01184 | 2.5e-123 | acuA | K | Part of the acuABC operon, which is possibly involved in the breakdown of acetoin and butanediol. Acts as an acetyltransferase inactivating acetyl-CoA synthetase AcsA via acetylation at a Lys residue | ||
BNJPHLCL_01185 | 3.8e-119 | acuB | S | Acetoin utilization protein AcuB | ||
BNJPHLCL_01186 | 1.6e-232 | acuC | BQ | histone deacetylase | ||
BNJPHLCL_01187 | 1.7e-182 | ccpA | K | catabolite control protein A | ||
BNJPHLCL_01188 | 1.4e-190 | aroF | 2.5.1.54, 5.4.99.5 | E | Catalyzes the formation of 3-deoxy-D-aribino-hept-2-ulosonate 7-phosphate from phosphoenolpyruvate and D-erythrose 4-phosphate and the formation of prephenate from chorismate | |
BNJPHLCL_01189 | 1.7e-34 | XK27_07760 | S | COG4980 Gas vesicle protein | ||
BNJPHLCL_01190 | 2.5e-44 | ytxG | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
BNJPHLCL_01191 | 2.2e-254 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
BNJPHLCL_01192 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
BNJPHLCL_01193 | 4.6e-71 | yhcN | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | ||
BNJPHLCL_01194 | 5.2e-110 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BNJPHLCL_01195 | 4.8e-148 | ytpQ | S | Belongs to the UPF0354 family | ||
BNJPHLCL_01196 | 1.9e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
BNJPHLCL_01197 | 7.5e-195 | rsbU | 3.1.3.3 | T | response regulator | |
BNJPHLCL_01198 | 8.9e-153 | cheR | 2.1.1.80 | NT | chemotaxis | |
BNJPHLCL_01199 | 0.0 | T | PhoQ Sensor | |||
BNJPHLCL_01200 | 6.6e-53 | ytzB | S | small secreted protein | ||
BNJPHLCL_01201 | 1.6e-170 | ytnP | S | COG0491 Zn-dependent hydrolases, including glyoxylases | ||
BNJPHLCL_01202 | 5.1e-130 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
BNJPHLCL_01203 | 1e-54 | ytzH | S | YtzH-like protein | ||
BNJPHLCL_01204 | 4.8e-156 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
BNJPHLCL_01206 | 1.5e-143 | ytlQ | ||||
BNJPHLCL_01207 | 2.3e-104 | ligT | 3.1.4.58, 3.5.1.42 | J | Hydrolyzes RNA 2',3'-cyclic phosphodiester to an RNA 2'- phosphomonoester | |
BNJPHLCL_01209 | 2.3e-159 | dat | 2.6.1.21 | E | Acts on the D-isomers of alanine, leucine, aspartate, glutamate, aminobutyrate, norvaline and asparagine. The enzyme transfers an amino group from a substrate D-amino acid to the pyridoxal phosphate cofactor to form pyridoxamine and an alpha- keto acid in the first half-reaction | |
BNJPHLCL_01210 | 1.7e-273 | pepV | 3.5.1.18 | E | Dipeptidase | |
BNJPHLCL_01211 | 1.2e-32 | ytzE | K | COG1349 Transcriptional regulators of sugar metabolism | ||
BNJPHLCL_01212 | 1.2e-286 | ytgP | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
BNJPHLCL_01213 | 6.4e-27 | yteV | S | Sporulation protein Cse60 | ||
BNJPHLCL_01214 | 5e-10 | |||||
BNJPHLCL_01216 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BNJPHLCL_01217 | 1.6e-187 | yttB | EGP | Major facilitator Superfamily | ||
BNJPHLCL_01218 | 9.4e-43 | ytzC | S | Protein of unknown function (DUF2524) | ||
BNJPHLCL_01220 | 2.9e-102 | ytqB | J | Putative rRNA methylase | ||
BNJPHLCL_01221 | 5.7e-208 | ytpB | 4.2.3.130 | S | Tetraprenyl-beta-curcumene synthase | |
BNJPHLCL_01222 | 4.5e-154 | ytpA | 3.1.1.5 | I | Alpha beta hydrolase | |
BNJPHLCL_01223 | 7.3e-73 | ytoA | S | COG0663 Carbonic anhydrases acetyltransferases, isoleucine patch superfamily | ||
BNJPHLCL_01224 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
BNJPHLCL_01225 | 3.2e-220 | 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 | |
BNJPHLCL_01226 | 5.3e-308 | pckA | 4.1.1.49 | C | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA | |
BNJPHLCL_01227 | 2e-67 | 3.6.1.55 | F | GDP-mannose mannosyl hydrolase activity | ||
BNJPHLCL_01228 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
BNJPHLCL_01229 | 1.7e-61 | |||||
BNJPHLCL_01230 | 1.3e-240 | ugtP | 2.4.1.315 | GT28 | M | Monogalactosyldiacylglycerol (MGDG) synthase |
BNJPHLCL_01231 | 2.9e-139 | pgdA | 3.5.1.104, 3.5.1.41 | G | Polysaccharide deacetylase | |
BNJPHLCL_01232 | 3.5e-100 | bcrC | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | |
BNJPHLCL_01233 | 3.1e-297 | katA | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
BNJPHLCL_01234 | 1.5e-189 | M1-600 | T | Putative diguanylate phosphodiesterase | ||
BNJPHLCL_01235 | 0.0 | swrC | V | Belongs to the resistance-nodulation-cell division (RND) (TC 2.A.6) family | ||
BNJPHLCL_01237 | 2.3e-281 | cls2 | I | PLD-like domain | ||
BNJPHLCL_01239 | 1.9e-53 | P | Domain of unknown function (DUF2935) | |||
BNJPHLCL_01240 | 6.3e-132 | ypmR1 | E | G-D-S-L family | ||
BNJPHLCL_01241 | 5.6e-169 | bcrA | V | ABC transporter, ATP-binding protein | ||
BNJPHLCL_01242 | 1.6e-174 | bcrB | S | ABC transporter (permease) | ||
BNJPHLCL_01243 | 6.4e-88 | |||||
BNJPHLCL_01244 | 1.1e-95 | 1.5.1.38 | S | FMN reductase | ||
BNJPHLCL_01245 | 2.1e-145 | 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 | |
BNJPHLCL_01246 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase | |
BNJPHLCL_01249 | 3.5e-149 | focA | P | Formate/nitrite transporter | ||
BNJPHLCL_01250 | 1.8e-22 | tcyC | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
BNJPHLCL_01251 | 2.1e-66 | tcyC | 3.6.3.21 | E | COG1126 ABC-type polar amino acid transport system, ATPase component | |
BNJPHLCL_01252 | 1.2e-115 | tcyB | P | COG0765 ABC-type amino acid transport system, permease component | ||
BNJPHLCL_01253 | 1.4e-144 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
BNJPHLCL_01254 | 2.4e-83 | S | Rubrerythrin | |||
BNJPHLCL_01255 | 1.6e-166 | ppaC | 3.6.1.1 | C | Inorganic pyrophosphatase | |
BNJPHLCL_01256 | 8.2e-103 | yvbG | U | UPF0056 membrane protein | ||
BNJPHLCL_01257 | 6e-221 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
BNJPHLCL_01258 | 1.1e-161 | yhbB | S | Putative amidase domain | ||
BNJPHLCL_01259 | 2e-88 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
BNJPHLCL_01260 | 0.0 | prkA | T | Ser protein kinase | ||
BNJPHLCL_01261 | 5.3e-220 | yhbH | S | Belongs to the UPF0229 family | ||
BNJPHLCL_01263 | 1.9e-98 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
BNJPHLCL_01264 | 3.4e-175 | pit | P | phosphate transporter | ||
BNJPHLCL_01265 | 5.6e-112 | ykaA | P | COG1392 Phosphate transport regulator (distant homolog of PhoU) | ||
BNJPHLCL_01266 | 1.2e-10 | yhcU | S | Family of unknown function (DUF5365) | ||
BNJPHLCL_01267 | 3.9e-66 | yhcU | S | Family of unknown function (DUF5365) | ||
BNJPHLCL_01268 | 5.8e-88 | bdbA | CO | Thioredoxin | ||
BNJPHLCL_01269 | 2.1e-73 | bdbC | O | Required for disulfide bond formation in some proteins | ||
BNJPHLCL_01270 | 1.6e-134 | 3.2.1.18 | GH33 | E | GDSL-like Lipase/Acylhydrolase | |
BNJPHLCL_01271 | 4.1e-181 | ykrP | G | COG3594 Fucose 4-O-acetylase and related acetyltransferases | ||
BNJPHLCL_01272 | 1.5e-274 | ycgB | S | Stage V sporulation protein R | ||
BNJPHLCL_01274 | 1.8e-46 | yhdB | S | YhdB-like protein | ||
BNJPHLCL_01275 | 2.5e-183 | corA | P | Mediates influx of magnesium ions | ||
BNJPHLCL_01276 | 9.2e-127 | S | Peptidase C26 | |||
BNJPHLCL_01277 | 4.1e-159 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BNJPHLCL_01278 | 4.1e-170 | dppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BNJPHLCL_01279 | 9.3e-189 | dppD | P | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_01280 | 0.0 | dppE | E | ABC transporter substrate-binding protein | ||
BNJPHLCL_01281 | 3.6e-176 | ykfC | 3.4.14.13 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
BNJPHLCL_01282 | 3.4e-191 | ykfD | E | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_01284 | 6.2e-85 | uspF | T | Universal stress protein | ||
BNJPHLCL_01285 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BNJPHLCL_01287 | 1.7e-31 | |||||
BNJPHLCL_01288 | 0.0 | yjgC | 1.17.1.10, 1.17.1.9 | C | formate dehydrogenase, alpha subunit | |
BNJPHLCL_01290 | 4.5e-56 | S | Protein of unknown function (DUF1641) | |||
BNJPHLCL_01291 | 1.3e-07 | S | Heavy-metal-associated domain | |||
BNJPHLCL_01293 | 8.5e-111 | 3.6.1.27 | I | COG0671 Membrane-associated phospholipid phosphatase | ||
BNJPHLCL_01294 | 6e-133 | ku | L | With LigD forms a non-homologous end joining (NHEJ) DNA repair enzyme, which repairs dsDNA breaks with reduced fidelity. Binds linear dsDNA with 5'- and 3'- overhangs but not closed circular dsDNA nor ssDNA. Recruits and stimulates the ligase activity of LigD | ||
BNJPHLCL_01295 | 0.0 | ligD | 6.5.1.1 | L | ATP-dependent DNA ligase | |
BNJPHLCL_01296 | 2.9e-182 | 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 | |
BNJPHLCL_01298 | 3.4e-242 | norM | V | Multidrug efflux pump | ||
BNJPHLCL_01299 | 5.4e-96 | ykwD | J | protein with SCP PR1 domains | ||
BNJPHLCL_01301 | 2.5e-66 | ypoP | K | transcriptional | ||
BNJPHLCL_01302 | 2.4e-270 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
BNJPHLCL_01303 | 2e-146 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
BNJPHLCL_01304 | 7.5e-25 | yozD | S | YozD-like protein | ||
BNJPHLCL_01305 | 4.3e-115 | yodN | ||||
BNJPHLCL_01306 | 7.5e-35 | yozE | S | Belongs to the UPF0346 family | ||
BNJPHLCL_01307 | 2.1e-191 | NT | CHASE3 domain | |||
BNJPHLCL_01308 | 1.2e-09 | S | Protein of unknown function (Tiny_TM_bacill) | |||
BNJPHLCL_01309 | 1.6e-78 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
BNJPHLCL_01310 | 1.6e-99 | 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 | |
BNJPHLCL_01311 | 6.1e-276 | rsmF | 2.1.1.176, 2.1.1.178 | J | RNA-binding PUA-like domain of methyltransferase RsmF | |
BNJPHLCL_01312 | 9.3e-98 | ypmS | S | protein conserved in bacteria | ||
BNJPHLCL_01313 | 1.2e-146 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
BNJPHLCL_01314 | 1.9e-110 | hlyIII | S | protein, Hemolysin III | ||
BNJPHLCL_01315 | 3.5e-93 | folA | 1.1.1.262, 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
BNJPHLCL_01316 | 4.3e-157 | 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 | |
BNJPHLCL_01317 | 1.3e-105 | ypjP | S | YpjP-like protein | ||
BNJPHLCL_01318 | 2.3e-75 | yphP | S | Belongs to the UPF0403 family | ||
BNJPHLCL_01319 | 1.3e-154 | ypgR | C | COG0694 Thioredoxin-like proteins and domains | ||
BNJPHLCL_01320 | 0.0 | yfmR | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
BNJPHLCL_01321 | 3.3e-86 | |||||
BNJPHLCL_01322 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
BNJPHLCL_01323 | 3e-72 | mntR | K | Involved in manganese homeostasis. Might activate the transcription of the mntABCD operon | ||
BNJPHLCL_01324 | 1.2e-31 | cspD | K | Cold-shock protein | ||
BNJPHLCL_01326 | 3.6e-27 | ypeQ | S | Zinc-finger | ||
BNJPHLCL_01327 | 4.6e-171 | polA | 2.7.7.7 | L | 5'3' exonuclease | |
BNJPHLCL_01328 | 2.1e-246 | ynbB | 4.4.1.1 | P | COG4100 Cystathionine beta-lyase family protein involved in aluminum resistance | |
BNJPHLCL_01329 | 3.7e-227 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
BNJPHLCL_01330 | 6e-174 | spoVK | O | stage V sporulation protein K | ||
BNJPHLCL_01331 | 1.2e-35 | hfq | J | RNA chaperone that binds small regulatory RNA (sRNAs) and mRNAs to facilitate mRNA translational regulation in response to envelope stress, environmental stress and changes in metabolite concentrations. Also binds with high specificity to tRNAs | ||
BNJPHLCL_01332 | 5.3e-187 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
BNJPHLCL_01335 | 1.1e-12 | 2.1.1.80, 3.1.1.61 | S | protein secretion by the type IV secretion system | ||
BNJPHLCL_01336 | 5.5e-40 | yhjA | S | Excalibur calcium-binding domain | ||
BNJPHLCL_01337 | 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 | ||
BNJPHLCL_01338 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
BNJPHLCL_01339 | 6.2e-99 | cotE | S | Outer spore coat protein E (CotE) | ||
BNJPHLCL_01340 | 2.1e-49 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
BNJPHLCL_01341 | 5.2e-300 | miaB | 2.8.4.3 | J | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
BNJPHLCL_01342 | 5.6e-212 | E | Amino acid permease | |||
BNJPHLCL_01343 | 5.5e-247 | yegQ | O | COG0826 Collagenase and related proteases | ||
BNJPHLCL_01344 | 3.7e-168 | yegQ | O | Peptidase U32 | ||
BNJPHLCL_01345 | 3.3e-37 | spoVS | S | Stage V sporulation protein S | ||
BNJPHLCL_01346 | 1.9e-152 | ymdB | S | protein conserved in bacteria | ||
BNJPHLCL_01347 | 1.2e-216 | rny | S | Endoribonuclease that initiates mRNA decay | ||
BNJPHLCL_01348 | 4.9e-188 | 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 | ||
BNJPHLCL_01349 | 2.4e-223 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
BNJPHLCL_01350 | 1.3e-99 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
BNJPHLCL_01351 | 1.1e-135 | ymfM | S | protein conserved in bacteria | ||
BNJPHLCL_01352 | 1e-142 | ymfK | S | Protein of unknown function (DUF3388) | ||
BNJPHLCL_01353 | 6.4e-41 | ymfJ | S | Protein of unknown function (DUF3243) | ||
BNJPHLCL_01354 | 5e-128 | 1.1.1.100 | S | Catalyzes the first of the two reduction steps in the elongation cycle of fatty acid synthesis | ||
BNJPHLCL_01355 | 2e-244 | ymfH | S | zinc protease | ||
BNJPHLCL_01356 | 2.1e-238 | ymfF | S | Peptidase M16 | ||
BNJPHLCL_01357 | 1.8e-170 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
BNJPHLCL_01358 | 5.8e-186 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
BNJPHLCL_01359 | 8e-285 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
BNJPHLCL_01360 | 9.1e-195 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
BNJPHLCL_01361 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
BNJPHLCL_01362 | 4.3e-35 | S | YlzJ-like protein | |||
BNJPHLCL_01363 | 2.2e-131 | tepA | 3.4.21.92 | OU | COG0740 Protease subunit of ATP-dependent Clp proteases | |
BNJPHLCL_01364 | 0.0 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
BNJPHLCL_01365 | 3.9e-159 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
BNJPHLCL_01366 | 1.1e-228 | dapG | 1.1.1.3, 2.7.2.4 | E | Belongs to the aspartokinase family | |
BNJPHLCL_01367 | 9.9e-194 | 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 | |
BNJPHLCL_01368 | 2.6e-109 | spoVFB | H | Together with DpaA, catalyzes the conversion of dihydrodipicolinate to dipicolinate (DPA) | ||
BNJPHLCL_01369 | 2.5e-186 | dpaA | 1.1.1.29, 1.1.1.399, 1.1.1.95 | CH | Dipicolinate synthase subunit A | |
BNJPHLCL_01370 | 1.4e-37 | ymxH | S | YlmC YmxH family | ||
BNJPHLCL_01371 | 2.4e-231 | pepR | S | Belongs to the peptidase M16 family | ||
BNJPHLCL_01372 | 1.2e-208 | ylxY | 3.5.1.104 | G | Sporulation protein, polysaccharide deacetylase | |
BNJPHLCL_01373 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
BNJPHLCL_01374 | 1e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
BNJPHLCL_01375 | 3.6e-182 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
BNJPHLCL_01376 | 2.4e-172 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
BNJPHLCL_01377 | 3.2e-56 | 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 | ||
BNJPHLCL_01378 | 8.6e-44 | ylxP | S | protein conserved in bacteria | ||
BNJPHLCL_01379 | 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 | ||
BNJPHLCL_01380 | 2.9e-48 | ylxQ | J | ribosomal protein | ||
BNJPHLCL_01381 | 8.2e-45 | ylxR | K | nucleic-acid-binding protein implicated in transcription termination | ||
BNJPHLCL_01382 | 2.8e-224 | nusA | K | Participates in both transcription termination and antitermination | ||
BNJPHLCL_01383 | 7.1e-83 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
BNJPHLCL_01384 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BNJPHLCL_01385 | 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 | |
BNJPHLCL_01386 | 3.3e-236 | rasP | M | zinc metalloprotease | ||
BNJPHLCL_01387 | 3.7e-194 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
BNJPHLCL_01388 | 3.2e-144 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
BNJPHLCL_01389 | 1.1e-147 | uppS | 2.5.1.31 | I | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BNJPHLCL_01390 | 6.9e-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 | ||
BNJPHLCL_01391 | 1.1e-127 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
BNJPHLCL_01392 | 1.8e-156 | 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 | ||
BNJPHLCL_01393 | 3.4e-135 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
BNJPHLCL_01394 | 2.4e-74 | ylxL | ||||
BNJPHLCL_01395 | 1.1e-136 | sigD | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
BNJPHLCL_01396 | 8.9e-84 | cheD | 3.5.1.44 | NT | Deamidates glutamine residues to glutamate on methyl- accepting chemotaxis receptors (MCPs). CheD-mediated MCP deamidation is required for productive communication of the conformational signals of the chemoreceptors to the CheA kinase | |
BNJPHLCL_01397 | 1.2e-112 | cheC | NT | COG1776 Chemotaxis protein CheC, inhibitor of MCP methylation | ||
BNJPHLCL_01398 | 8.2e-70 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
BNJPHLCL_01399 | 0.0 | cheA | 2.7.13.3 | NT | COG0643 Chemotaxis protein histidine kinase and related kinases | |
BNJPHLCL_01400 | 3.2e-113 | cheB | 3.1.1.61, 3.5.1.44 | NT | catalyzes the demethylation of specific methylglutamate residues introduced into the chemoreceptors (methyl-accepting chemotaxis proteins) by CheR | |
BNJPHLCL_01401 | 1.2e-144 | flhG | D | Belongs to the ParA family | ||
BNJPHLCL_01402 | 4.9e-194 | flhF | N | Flagellar biosynthesis regulator FlhF | ||
BNJPHLCL_01403 | 0.0 | flhA | N | Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
BNJPHLCL_01404 | 3.5e-186 | flhB | N | Required for formation of the rod structure in the basal body of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin | ||
BNJPHLCL_01405 | 8.6e-134 | fliR | N | Flagellar biosynthetic protein FliR | ||
BNJPHLCL_01406 | 1.5e-37 | fliQ | N | Role in flagellar biosynthesis | ||
BNJPHLCL_01407 | 2.6e-107 | fliP | N | Plays a role in the flagellum-specific transport system | ||
BNJPHLCL_01408 | 3.2e-116 | fliZ | N | Flagellar biosynthesis protein, FliO | ||
BNJPHLCL_01409 | 2.1e-58 | cheB | 3.1.1.61, 3.5.1.44 | T | response regulator | |
BNJPHLCL_01410 | 1.2e-173 | fliN | N | FliN is one of three proteins (FliG, FliN, FliM) that form the rotor-mounted switch complex (C ring), located at the base of the basal body. This complex interacts with the CheY and CheZ chemotaxis proteins, in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
BNJPHLCL_01411 | 3.4e-183 | fliM | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
BNJPHLCL_01412 | 1.3e-64 | fliL | N | Controls the rotational direction of flagella during chemotaxis | ||
BNJPHLCL_01413 | 3.1e-115 | flgG | N | Flagellar basal body rod | ||
BNJPHLCL_01414 | 3.2e-72 | flg | N | Putative flagellar | ||
BNJPHLCL_01415 | 2.3e-108 | flgD | N | Flagellar basal body rod modification protein | ||
BNJPHLCL_01416 | 6.9e-292 | fliK | N | Flagellar hook-length control | ||
BNJPHLCL_01417 | 2.7e-37 | ylxF | S | MgtE intracellular N domain | ||
BNJPHLCL_01418 | 1.6e-68 | fliJ | N | Flagellar biosynthesis chaperone | ||
BNJPHLCL_01419 | 7.3e-242 | fliI | 3.6.3.14 | NU | COG1157 Flagellar biosynthesis type III secretory pathway ATPase | |
BNJPHLCL_01420 | 3.5e-124 | fliH | NU | COG1317 Flagellar biosynthesis type III secretory pathway protein | ||
BNJPHLCL_01421 | 1.1e-162 | fliG | N | One of the proteins that forms a switch complex that is proposed to be located at the base of the basal body. This complex interacts with chemotaxis proteins (such as CheY) in addition to contacting components of the motor that determine the direction of flagellar rotation | ||
BNJPHLCL_01422 | 6.5e-245 | fliF | N | The M ring may be actively involved in energy transduction | ||
BNJPHLCL_01423 | 6.4e-40 | fliE | N | Flagellar hook-basal body complex protein FliE | ||
BNJPHLCL_01424 | 4e-75 | flgC | N | Belongs to the flagella basal body rod proteins family | ||
BNJPHLCL_01425 | 5.7e-62 | flgB | N | Structural component of flagellum, the bacterial motility apparatus. Part of the rod structure of flagellar basal body | ||
BNJPHLCL_01426 | 3.3e-133 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
BNJPHLCL_01427 | 2.1e-226 | 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 | ||
BNJPHLCL_01428 | 7.4e-92 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
BNJPHLCL_01429 | 4.3e-169 | xerC | L | tyrosine recombinase XerC | ||
BNJPHLCL_01430 | 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 | |
BNJPHLCL_01431 | 6.3e-56 | cas5d | S | CRISPR-associated protein (Cas_Cas5) | ||
BNJPHLCL_01432 | 3.4e-146 | yjaZ | O | Zn-dependent protease | ||
BNJPHLCL_01433 | 1.9e-29 | yodI | ||||
BNJPHLCL_01435 | 1.3e-88 | L | Transposase IS116/IS110/IS902 family | |||
BNJPHLCL_01436 | 3.2e-193 | S | AI-2E family transporter | |||
BNJPHLCL_01437 | 1.7e-109 | lmrB | EGP | the major facilitator superfamily | ||
BNJPHLCL_01438 | 9e-224 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_01439 | 8e-102 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
BNJPHLCL_01440 | 7.1e-23 | S | double-stranded DNA endodeoxyribonuclease activity | |||
BNJPHLCL_01442 | 3.8e-75 | mgsA | 2.7.1.24, 4.2.3.3 | G | methylglyoxal synthase | |
BNJPHLCL_01443 | 6.8e-16 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
BNJPHLCL_01444 | 6.8e-209 | L | Transposase IS4 family protein | |||
BNJPHLCL_01445 | 2.6e-166 | S | Nuclease-related domain | |||
BNJPHLCL_01447 | 3.2e-110 | 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) | |
BNJPHLCL_01448 | 3.3e-124 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
BNJPHLCL_01449 | 4e-181 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
BNJPHLCL_01450 | 2.8e-140 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
BNJPHLCL_01451 | 0.0 | carB | 6.3.5.5 | F | Belongs to the CarB family | |
BNJPHLCL_01452 | 3.8e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
BNJPHLCL_01453 | 1.3e-248 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
BNJPHLCL_01454 | 1.2e-166 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
BNJPHLCL_01455 | 9.7e-92 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
BNJPHLCL_01456 | 7.9e-179 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BNJPHLCL_01457 | 1.3e-82 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
BNJPHLCL_01459 | 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) | |
BNJPHLCL_01460 | 2.5e-65 | divIVA | D | Cell division initiation protein | ||
BNJPHLCL_01461 | 3.7e-145 | ylmH | 5.4.99.23, 5.4.99.24 | S | conserved protein, contains S4-like domain | |
BNJPHLCL_01462 | 1.4e-38 | yggT | S | membrane | ||
BNJPHLCL_01463 | 1.1e-64 | 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 | ||
BNJPHLCL_01464 | 7.3e-121 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
BNJPHLCL_01465 | 8.2e-159 | yfiH | S | Belongs to the multicopper oxidase YfiH RL5 family | ||
BNJPHLCL_01466 | 2.6e-73 | yocH | CBM50 | M | 3D domain | |
BNJPHLCL_01467 | 1.5e-43 | ylmC | S | sporulation protein | ||
BNJPHLCL_01468 | 9.6e-13 | S | Domain of unknown function (DUF4305) | |||
BNJPHLCL_01469 | 2.9e-123 | ydiL | S | CAAX protease self-immunity | ||
BNJPHLCL_01470 | 5.7e-43 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
BNJPHLCL_01471 | 1.6e-283 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
BNJPHLCL_01472 | 4.1e-68 | yngA | S | GtrA-like protein | ||
BNJPHLCL_01473 | 6.6e-187 | ykoT | GT2 | M | COG0463 Glycosyltransferases involved in cell wall biogenesis | |
BNJPHLCL_01474 | 0.0 | ykoS | ||||
BNJPHLCL_01475 | 4.7e-199 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
BNJPHLCL_01476 | 2.4e-106 | pncA | Q | COG1335 Amidases related to nicotinamidase | ||
BNJPHLCL_01477 | 9.4e-283 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
BNJPHLCL_01478 | 8e-154 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
BNJPHLCL_01480 | 1.2e-299 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
BNJPHLCL_01481 | 7.7e-31 | S | Domain of unknown function (DUF4177) | |||
BNJPHLCL_01482 | 4.7e-31 | |||||
BNJPHLCL_01483 | 1.4e-27 | K | Helix-turn-helix domain | |||
BNJPHLCL_01484 | 8.8e-63 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_01485 | 0.0 | ygaD | V | ABC transporter | ||
BNJPHLCL_01486 | 4.1e-103 | ygaC | J | Belongs to the UPF0374 family | ||
BNJPHLCL_01487 | 1.3e-35 | ygaB | S | YgaB-like protein | ||
BNJPHLCL_01488 | 1.7e-08 | sspE | S | Small, acid-soluble spore protein, gamma-type | ||
BNJPHLCL_01489 | 7.7e-132 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_01490 | 1.7e-165 | gltC | K | Transcriptional regulator | ||
BNJPHLCL_01491 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase | |
BNJPHLCL_01493 | 6.1e-282 | gltD | 1.4.1.13, 1.4.1.14 | E | COG0493 NADPH-dependent glutamate synthase beta chain and related oxidoreductases | |
BNJPHLCL_01494 | 8.8e-31 | |||||
BNJPHLCL_01495 | 3.1e-198 | mutY | L | A G-specific | ||
BNJPHLCL_01496 | 2.9e-179 | yfhP | S | membrane-bound metal-dependent | ||
BNJPHLCL_01497 | 4.2e-19 | sspK | S | reproduction | ||
BNJPHLCL_01498 | 3.5e-49 | yfhH | S | Protein of unknown function (DUF1811) | ||
BNJPHLCL_01499 | 1.8e-131 | recX | 2.4.1.337 | GT4 | S | Modulates RecA activity |
BNJPHLCL_01501 | 3.2e-24 | yfhD | S | YfhD-like protein | ||
BNJPHLCL_01502 | 6.9e-139 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
BNJPHLCL_01504 | 1.6e-227 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
BNJPHLCL_01505 | 1.2e-245 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpC family | |
BNJPHLCL_01506 | 1.1e-181 | trpD | 2.4.2.18, 4.1.3.27 | E | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
BNJPHLCL_01507 | 5.3e-107 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Anthranilate synthase | |
BNJPHLCL_01508 | 9.5e-261 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
BNJPHLCL_01509 | 3.8e-48 | bacI | V | COG0577 ABC-type antimicrobial peptide transport system, permease component | ||
BNJPHLCL_01510 | 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 |
BNJPHLCL_01512 | 7e-241 | mcpA | NT | chemotaxis protein | ||
BNJPHLCL_01513 | 2.8e-182 | serA1 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
BNJPHLCL_01514 | 4e-220 | dhsS | 1.12.1.2 | E | COG0075 Serine-pyruvate aminotransferase archaeal aspartate aminotransferase | |
BNJPHLCL_01515 | 1e-301 | serA | 1.1.1.399, 1.1.1.95 | E | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BNJPHLCL_01516 | 1.5e-178 | S | Phosphotransferase system, EIIC | |||
BNJPHLCL_01517 | 3.3e-219 | 2.6.1.9 | S | HAD-hyrolase-like | ||
BNJPHLCL_01518 | 7.4e-189 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
BNJPHLCL_01519 | 7.8e-111 | leuD | 4.2.1.33, 4.2.1.35, 4.2.1.36 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
BNJPHLCL_01520 | 9.7e-269 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
BNJPHLCL_01521 | 1.7e-199 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
BNJPHLCL_01522 | 1.3e-282 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
BNJPHLCL_01523 | 1.8e-195 | ilvC | 1.1.1.86 | EH | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
BNJPHLCL_01524 | 1.1e-84 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
BNJPHLCL_01525 | 0.0 | ilvB | 2.2.1.6 | E | Acetolactate synthase | |
BNJPHLCL_01526 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
BNJPHLCL_01527 | 4.6e-244 | braB | E | Component of the transport system for branched-chain amino acids | ||
BNJPHLCL_01528 | 3.8e-151 | T | STAS domain | |||
BNJPHLCL_01529 | 4.6e-246 | |||||
BNJPHLCL_01530 | 2.1e-37 | cypC | 1.11.2.4, 1.14.14.1 | Q | Cytochrome P450 | |
BNJPHLCL_01531 | 2.6e-104 | yetJ | S | Belongs to the BI1 family | ||
BNJPHLCL_01532 | 7e-214 | yxjG | 2.1.1.14 | E | Methionine synthase | |
BNJPHLCL_01533 | 2.3e-218 | yhjX | P | Major facilitator superfamily | ||
BNJPHLCL_01534 | 2.1e-137 | ypdB | KT | LytTr DNA-binding domain | ||
BNJPHLCL_01535 | 7.5e-308 | ypdA | 2.7.13.3 | T | Signal transduction histidine kinase | |
BNJPHLCL_01536 | 3.6e-193 | ansA | 3.5.1.1 | EJ | L-asparaginase | |
BNJPHLCL_01537 | 0.0 | cotA | 1.10.3.4, 1.16.3.3 | Q | multicopper oxidases | |
BNJPHLCL_01538 | 3.8e-20 | yhgD | K | Transcriptional regulator | ||
BNJPHLCL_01539 | 2.3e-54 | yhgE | S | YhgE Pip N-terminal domain protein | ||
BNJPHLCL_01540 | 6.6e-248 | S | Protein of unknown function N-terminus (DUF3323) | |||
BNJPHLCL_01541 | 0.0 | D | Putative exonuclease SbcCD, C subunit | |||
BNJPHLCL_01542 | 6.8e-85 | D | Putative exonuclease SbcCD, C subunit | |||
BNJPHLCL_01543 | 2.4e-228 | S | Protein of unknown function (DUF2398) | |||
BNJPHLCL_01545 | 8.6e-260 | S | Protein of unknown function (DUF2397) | |||
BNJPHLCL_01546 | 1.6e-13 | yoaT | S | Protein of unknown function (DUF817) | ||
BNJPHLCL_01547 | 5.1e-28 | yozG | K | Transcriptional regulator | ||
BNJPHLCL_01548 | 1.6e-69 | yoaS | S | Protein of unknown function (DUF2975) | ||
BNJPHLCL_01549 | 4.2e-43 | |||||
BNJPHLCL_01550 | 5.6e-237 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
BNJPHLCL_01551 | 8.6e-76 | yqgC | S | protein conserved in bacteria | ||
BNJPHLCL_01552 | 3.6e-274 | ydbT | S | Bacterial PH domain | ||
BNJPHLCL_01553 | 9.4e-86 | S | Bacterial PH domain | |||
BNJPHLCL_01554 | 9.6e-86 | S | AAA domain | |||
BNJPHLCL_01555 | 2.8e-31 | yhcC | S | nucleic-acid-binding protein containing a Zn-ribbon domain | ||
BNJPHLCL_01556 | 1.2e-188 | yfjN | 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 | ||
BNJPHLCL_01557 | 1.1e-64 | argO | S | Lysine exporter protein LysE YggA | ||
BNJPHLCL_01558 | 7.2e-110 | sigH | K | Belongs to the sigma-70 factor family | ||
BNJPHLCL_01559 | 6.6e-24 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
BNJPHLCL_01560 | 9.2e-95 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
BNJPHLCL_01561 | 1.4e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
BNJPHLCL_01562 | 4.3e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
BNJPHLCL_01563 | 1e-08 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
BNJPHLCL_01564 | 5.4e-81 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
BNJPHLCL_01565 | 3e-52 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
BNJPHLCL_01566 | 6.5e-113 | rsmC | 2.1.1.172 | J | Methyltransferase | |
BNJPHLCL_01567 | 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 | |
BNJPHLCL_01568 | 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 | |
BNJPHLCL_01569 | 1.2e-36 | rplGB | J | Belongs to the eukaryotic ribosomal protein eL8 family | ||
BNJPHLCL_01570 | 8.6e-72 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
BNJPHLCL_01571 | 9.3e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
BNJPHLCL_01572 | 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 | ||
BNJPHLCL_01573 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
BNJPHLCL_01574 | 3.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
BNJPHLCL_01575 | 2.6e-112 | 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 | ||
BNJPHLCL_01576 | 1.1e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
BNJPHLCL_01577 | 6.3e-42 | 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 | ||
BNJPHLCL_01578 | 1.5e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
BNJPHLCL_01579 | 2.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
BNJPHLCL_01580 | 6.6e-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 | ||
BNJPHLCL_01581 | 1.4e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
BNJPHLCL_01582 | 9.2e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
BNJPHLCL_01583 | 2.7e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
BNJPHLCL_01584 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
BNJPHLCL_01585 | 1.5e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
BNJPHLCL_01586 | 9.6e-52 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
BNJPHLCL_01587 | 1.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
BNJPHLCL_01588 | 5.8e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
BNJPHLCL_01589 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
BNJPHLCL_01590 | 1.1e-92 | 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 | ||
BNJPHLCL_01591 | 2.3e-57 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
BNJPHLCL_01592 | 6.2e-85 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
BNJPHLCL_01593 | 4.1e-23 | rpmD | J | Ribosomal protein L30 | ||
BNJPHLCL_01594 | 1.2e-71 | rplO | J | binds to the 23S rRNA | ||
BNJPHLCL_01595 | 6.9e-229 | 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 | ||
BNJPHLCL_01596 | 9.7e-123 | 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 | |
BNJPHLCL_01597 | 2.4e-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 | ||
BNJPHLCL_01598 | 1.8e-57 | 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 | ||
BNJPHLCL_01599 | 2e-62 | 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 | ||
BNJPHLCL_01600 | 2.6e-211 | csd1 | 3.5.1.28 | M | CRISPR-associated protein (Cas_Csd1) | |
BNJPHLCL_01601 | 9.5e-134 | csd2 | L | CRISPR-associated protein | ||
BNJPHLCL_01602 | 4.9e-98 | cas4 | 3.1.12.1 | L | RecB family exonuclease | |
BNJPHLCL_01603 | 2.8e-172 | 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 | ||
BNJPHLCL_01604 | 5.8e-39 | 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 | ||
BNJPHLCL_01605 | 3.4e-135 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BNJPHLCL_01606 | 1.6e-59 | rplQ | J | Ribosomal protein L17 | ||
BNJPHLCL_01607 | 1.1e-156 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
BNJPHLCL_01608 | 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 | |
BNJPHLCL_01609 | 2.7e-138 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
BNJPHLCL_01610 | 3.2e-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 | |
BNJPHLCL_01611 | 3.8e-78 | 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 | ||
BNJPHLCL_01612 | 1.6e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
BNJPHLCL_01613 | 5.7e-09 | S | Protein conserved in bacteria | |||
BNJPHLCL_01615 | 1.9e-225 | sat | 2.7.7.4 | P | Belongs to the sulfate adenylyltransferase family | |
BNJPHLCL_01616 | 1.1e-110 | cysC | 2.7.1.25, 2.7.7.4 | P | Catalyzes the synthesis of activated sulfate | |
BNJPHLCL_01617 | 6.8e-273 | lysP | E | amino acid | ||
BNJPHLCL_01618 | 9.7e-82 | ybaK | S | Protein of unknown function (DUF2521) | ||
BNJPHLCL_01619 | 2.4e-130 | cwlD | 3.5.1.28 | M | n-acetylmuramoyl-L-alanine amidase | |
BNJPHLCL_01620 | 1.9e-197 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
BNJPHLCL_01622 | 1.4e-61 | gerD | S | Spore gernimation protein | ||
BNJPHLCL_01623 | 2.3e-100 | kbaA | 2.7.8.43 | S | Involved in the activation of the KinB signaling pathway of sporulation | |
BNJPHLCL_01624 | 5.3e-211 | S | Acyl-coenzyme A:6-aminopenicillanic acid acyl-transferase | |||
BNJPHLCL_01625 | 1.3e-173 | K | Transcriptional regulator | |||
BNJPHLCL_01626 | 1.2e-58 | yrkC | G | Cupin domain | ||
BNJPHLCL_01627 | 1.5e-300 | dppE_1 | E | ABC transporter substrate-binding protein | ||
BNJPHLCL_01628 | 4.4e-153 | oppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BNJPHLCL_01629 | 1.2e-180 | oppC | EP | COG1173 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BNJPHLCL_01630 | 1.5e-197 | oppD | P | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_01631 | 3e-173 | oppF | E | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_01632 | 1.6e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
BNJPHLCL_01633 | 1.7e-119 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis. Acts negatively in the development of competence by binding ComK and recruiting it to the ClpCP protease. When overexpressed, inhibits sporulation. Also involved in Spx degradation by ClpC | ||
BNJPHLCL_01634 | 2.6e-226 | yjbF | S | Competence protein | ||
BNJPHLCL_01635 | 0.0 | pepF | E | oligoendopeptidase F | ||
BNJPHLCL_01637 | 1.2e-160 | yjbH | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
BNJPHLCL_01638 | 4.4e-73 | yjbI | S | COG2346 Truncated hemoglobins | ||
BNJPHLCL_01639 | 4.5e-98 | yjbJ | M | COG0741 Soluble lytic murein transglycosylase and related regulatory proteins (some contain LysM invasin domains) | ||
BNJPHLCL_01640 | 1.1e-101 | yjbK | S | protein conserved in bacteria | ||
BNJPHLCL_01641 | 4.9e-66 | yjbL | S | Belongs to the UPF0738 family | ||
BNJPHLCL_01642 | 9.4e-121 | yjbM | 2.7.6.5 | S | GTP pyrophosphokinase | |
BNJPHLCL_01643 | 4.9e-153 | nadK | 2.7.1.23 | G | 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 | |
BNJPHLCL_01644 | 1.5e-163 | yjbO | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BNJPHLCL_01645 | 3.1e-138 | prpE | 3.6.1.41 | T | Asymmetrically hydrolyzes Ap4p to yield AMP and ATP | |
BNJPHLCL_01646 | 7.3e-141 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
BNJPHLCL_01648 | 1.6e-06 | yjbX | S | Spore coat protein CotO | ||
BNJPHLCL_01649 | 3.9e-83 | cotY | S | Spore coat protein | ||
BNJPHLCL_01650 | 8.4e-60 | S | Protein of unknown function (DUF1360) | |||
BNJPHLCL_01652 | 3.6e-79 | S | Sporulation lipoprotein YhcN/YlaJ (Spore_YhcN_YlaJ) | |||
BNJPHLCL_01653 | 1.6e-82 | spoVAC | S | stage V sporulation protein AC | ||
BNJPHLCL_01654 | 5.1e-187 | spoVAD | I | Stage V sporulation protein AD | ||
BNJPHLCL_01655 | 3.3e-56 | spoVAE | S | stage V sporulation protein | ||
BNJPHLCL_01657 | 4.5e-39 | spoVIF | S | Stage VI sporulation protein F | ||
BNJPHLCL_01659 | 2.3e-72 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
BNJPHLCL_01660 | 2.4e-92 | yjcG | J | Belongs to the 2H phosphoesterase superfamily. YjcG family | ||
BNJPHLCL_01661 | 2.1e-134 | yjcH | P | COG2382 Enterochelin esterase and related enzymes | ||
BNJPHLCL_01667 | 4.6e-168 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
BNJPHLCL_01668 | 4.1e-78 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BNJPHLCL_01669 | 2e-166 | yhaQ | S | ABC transporter, ATP-binding protein | ||
BNJPHLCL_01670 | 2.6e-209 | yhaP | CP | COG1668 ABC-type Na efflux pump, permease component | ||
BNJPHLCL_01671 | 4.7e-257 | pepC | 3.4.22.40 | E | Papain family cysteine protease | |
BNJPHLCL_01672 | 0.0 | pepF2 | E | COG1164 Oligoendopeptidase F | ||
BNJPHLCL_01673 | 7e-34 | ykuS | S | Belongs to the UPF0180 family | ||
BNJPHLCL_01674 | 0.0 | 6.2.1.1, 6.2.1.16 | I | AMP-dependent synthetase | ||
BNJPHLCL_01675 | 9e-90 | ywrA | P | COG2059 Chromate transport protein ChrA | ||
BNJPHLCL_01676 | 5.9e-98 | chrA | P | Chromate transporter | ||
BNJPHLCL_01677 | 3.6e-82 | ywrC | K | Transcriptional regulator | ||
BNJPHLCL_01678 | 1.4e-37 | L | Belongs to the 'phage' integrase family | |||
BNJPHLCL_01680 | 4.7e-144 | pocR | K | Sensory domain found in PocR | ||
BNJPHLCL_01681 | 1.8e-223 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BNJPHLCL_01682 | 1.2e-210 | yxjG | 2.1.1.14 | E | Methionine synthase | |
BNJPHLCL_01683 | 7.7e-231 | esaA | S | domain protein | ||
BNJPHLCL_01685 | 4.4e-39 | yukD | S | WXG100 protein secretion system (Wss), protein YukD | ||
BNJPHLCL_01686 | 1.5e-218 | essB | S | WXG100 protein secretion system (Wss), protein YukC | ||
BNJPHLCL_01687 | 0.0 | essC | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | ||
BNJPHLCL_01688 | 9.7e-154 | S | Protein of unknown function (DUF1646) | |||
BNJPHLCL_01689 | 0.0 | asnO | 6.3.5.4 | E | Asparagine synthase | |
BNJPHLCL_01690 | 9.9e-177 | ywbI | K | Transcriptional regulator | ||
BNJPHLCL_01691 | 5e-55 | ywbH | S | LrgA family | ||
BNJPHLCL_01692 | 3.8e-117 | ywbG | M | effector of murein hydrolase | ||
BNJPHLCL_01694 | 3.3e-115 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
BNJPHLCL_01695 | 2.4e-77 | |||||
BNJPHLCL_01696 | 2e-33 | T | Two component transcriptional regulator, winged helix family | |||
BNJPHLCL_01697 | 1e-78 | T | Two component transcriptional regulator, winged helix family | |||
BNJPHLCL_01698 | 8e-230 | T | His Kinase A (phosphoacceptor) domain | |||
BNJPHLCL_01699 | 7.7e-14 | |||||
BNJPHLCL_01700 | 1.8e-161 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BNJPHLCL_01701 | 3.7e-154 | ybbH_2 | K | Transcriptional regulator | ||
BNJPHLCL_01702 | 7.7e-233 | phoA | 3.1.3.1 | P | Belongs to the alkaline phosphatase family | |
BNJPHLCL_01703 | 0.0 | recQ | 3.6.4.12 | L | DNA helicase | |
BNJPHLCL_01704 | 4.4e-163 | ycsE | S | hydrolases of the HAD superfamily | ||
BNJPHLCL_01705 | 1.6e-128 | bshB2 | S | deacetylase | ||
BNJPHLCL_01706 | 5.7e-61 | yojF | S | Protein of unknown function (DUF1806) | ||
BNJPHLCL_01707 | 6.2e-151 | thiD | 2.5.1.3, 2.7.1.35, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BNJPHLCL_01708 | 1e-156 | K | Helix-turn-helix domain, rpiR family | |||
BNJPHLCL_01709 | 2.9e-215 | amhX | S | amidohydrolase | ||
BNJPHLCL_01710 | 6.8e-158 | 4.2.3.5 | M | carboxylic acid catabolic process | ||
BNJPHLCL_01711 | 1.2e-216 | menC | 4.2.1.113 | H | Converts 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1- carboxylate (SHCHC) to 2-succinylbenzoate (OSB) | |
BNJPHLCL_01712 | 7.6e-165 | S | membrane | |||
BNJPHLCL_01713 | 1.4e-26 | L | PFAM Integrase, catalytic core | |||
BNJPHLCL_01714 | 1e-88 | S | NYN domain | |||
BNJPHLCL_01715 | 1.9e-16 | focA | P | Formate nitrite | ||
BNJPHLCL_01716 | 1.5e-115 | focA | P | Formate nitrite | ||
BNJPHLCL_01717 | 1.6e-149 | cbiQ | P | COG0619 ABC-type cobalt transport system, permease component CbiQ and related transporters | ||
BNJPHLCL_01718 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
BNJPHLCL_01719 | 6.8e-93 | S | UPF0397 protein | |||
BNJPHLCL_01720 | 1.5e-163 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
BNJPHLCL_01721 | 5.3e-59 | xylS | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
BNJPHLCL_01722 | 4.9e-295 | Otg1 | S | Predicted membrane protein (DUF2339) | ||
BNJPHLCL_01723 | 2e-52 | |||||
BNJPHLCL_01725 | 9.7e-152 | 3.1.4.46, 5.4.2.11 | C | glycerophosphoryl diester phosphodiesterase | ||
BNJPHLCL_01726 | 3.8e-195 | S | Metallo-beta-lactamase superfamily | |||
BNJPHLCL_01727 | 3.5e-135 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
BNJPHLCL_01728 | 2.3e-134 | phnE | 3.6.1.63 | P | ABC transporter | |
BNJPHLCL_01729 | 3.7e-20 | phnE | 3.6.1.63 | P | ABC transporter | |
BNJPHLCL_01730 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
BNJPHLCL_01731 | 0.0 | yjcD | 3.6.4.12 | L | DNA helicase | |
BNJPHLCL_01732 | 4.6e-225 | ywdJ | F | Xanthine uracil | ||
BNJPHLCL_01733 | 7.2e-167 | ytnM | S | membrane transporter protein | ||
BNJPHLCL_01734 | 8.1e-241 | E | COG1113 Gamma-aminobutyrate permease and related permeases | |||
BNJPHLCL_01735 | 8.8e-136 | nfrA | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
BNJPHLCL_01736 | 0.0 | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | |||
BNJPHLCL_01737 | 6.3e-190 | amiE | 3.5.1.4 | S | Carbon-nitrogen hydrolase | |
BNJPHLCL_01738 | 4.1e-309 | F | COG1457 Purine-cytosine permease and related proteins | |||
BNJPHLCL_01739 | 6.8e-200 | amiF | 3.5.1.49 | S | Is an aliphatic amidase with a restricted substrate specificity, as it only hydrolyzes formamide | |
BNJPHLCL_01740 | 3.7e-48 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
BNJPHLCL_01741 | 6.7e-56 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
BNJPHLCL_01742 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
BNJPHLCL_01743 | 6e-79 | ureE | O | Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly | ||
BNJPHLCL_01744 | 1.6e-104 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
BNJPHLCL_01745 | 7.3e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
BNJPHLCL_01746 | 9.9e-157 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
BNJPHLCL_01747 | 6.1e-112 | ureH | S | PFAM Nickel cobalt transporter, high-affinity | ||
BNJPHLCL_01748 | 2.6e-173 | pfoS | S | Phosphotransferase system, EIIC | ||
BNJPHLCL_01749 | 8.8e-184 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase DhaK, subunit | |
BNJPHLCL_01750 | 3.6e-100 | dhaL | 2.7.1.121 | S | Dak2 | |
BNJPHLCL_01751 | 2.6e-59 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
BNJPHLCL_01752 | 1e-246 | gabT | 2.6.1.19, 2.6.1.22 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
BNJPHLCL_01753 | 2.6e-189 | puuP | E | Amino acid permease | ||
BNJPHLCL_01754 | 7.9e-82 | S | Carbon-nitrogen hydrolase | |||
BNJPHLCL_01755 | 2.3e-82 | yjjM | K | FCD | ||
BNJPHLCL_01756 | 2e-29 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
BNJPHLCL_01757 | 2.1e-73 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
BNJPHLCL_01758 | 3.8e-70 | ywnF | S | Family of unknown function (DUF5392) | ||
BNJPHLCL_01760 | 2.2e-204 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
BNJPHLCL_01761 | 8.7e-255 | iolT | EGP | Major facilitator Superfamily | ||
BNJPHLCL_01762 | 7.8e-85 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | |||
BNJPHLCL_01763 | 3.5e-57 | ygbA | S | Nitrous oxide-stimulated promoter | ||
BNJPHLCL_01764 | 2.5e-152 | yidA | S | hydrolases of the HAD superfamily | ||
BNJPHLCL_01765 | 8.2e-32 | |||||
BNJPHLCL_01766 | 3.2e-95 | D | Hemerythrin HHE cation binding | |||
BNJPHLCL_01767 | 3.8e-204 | gldA | 1.1.1.6 | C | COG0371 Glycerol dehydrogenase and related enzymes | |
BNJPHLCL_01768 | 1.3e-131 | fruR | K | Transcriptional regulator | ||
BNJPHLCL_01769 | 0.0 | fruA | 2.7.1.202 | GT | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
BNJPHLCL_01770 | 0.0 | yjcE | P | COG0025 NhaP-type Na H and K H antiporters | ||
BNJPHLCL_01771 | 6e-35 | yoeD | G | Helix-turn-helix domain | ||
BNJPHLCL_01772 | 4.8e-117 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
BNJPHLCL_01773 | 6.2e-210 | fni | 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) | |
BNJPHLCL_01775 | 2e-88 | 1.8.5.2 | S | DoxX | ||
BNJPHLCL_01776 | 4e-107 | C | Nitroreductase family | |||
BNJPHLCL_01777 | 0.0 | snf | 2.7.11.1 | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | |
BNJPHLCL_01778 | 0.0 | cas3 | L | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BNJPHLCL_01779 | 1.6e-47 | cas5d | S | CRISPR-associated protein (Cas_Cas5) | ||
BNJPHLCL_01780 | 2.2e-111 | ccpN | K | CBS domain | ||
BNJPHLCL_01781 | 5.5e-144 | yqfL | 2.7.11.33, 2.7.4.28 | S | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
BNJPHLCL_01782 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
BNJPHLCL_01783 | 2.8e-202 | 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 | ||
BNJPHLCL_01784 | 6.4e-88 | |||||
BNJPHLCL_01785 | 1.5e-64 | cccA | C | Cytochrome C oxidase, cbb3-type, subunit III | ||
BNJPHLCL_01786 | 6.6e-119 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
BNJPHLCL_01787 | 8.4e-207 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
BNJPHLCL_01788 | 9.8e-180 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
BNJPHLCL_01790 | 7.2e-242 | 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 | |
BNJPHLCL_01791 | 1.5e-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 | |
BNJPHLCL_01792 | 1.8e-126 | cwlO | CBM50 | M | protein conserved in bacteria | |
BNJPHLCL_01793 | 1e-19 | yqfT | S | Protein of unknown function (DUF2624) | ||
BNJPHLCL_01794 | 2.7e-140 | zurA | P | 'COG1121 ABC-type Mn Zn transport systems, ATPase component' | ||
BNJPHLCL_01795 | 4e-140 | znuB | P | COG1108 ABC-type Mn2 Zn2 transport systems, permease components | ||
BNJPHLCL_01796 | 1.5e-74 | zur | P | Belongs to the Fur family | ||
BNJPHLCL_01797 | 4.4e-114 | yqfW | S | Belongs to the 5'(3')-deoxyribonucleotidase family | ||
BNJPHLCL_01798 | 6.8e-201 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
BNJPHLCL_01799 | 4.4e-55 | fimV | NU | Tfp pilus assembly protein FimV | ||
BNJPHLCL_01800 | 3.7e-116 | sodA | 1.15.1.1 | P | radicals which are normally produced within the cells and which are toxic to biological systems | |
BNJPHLCL_01801 | 1.2e-219 | yqgE | EGP | Major facilitator superfamily | ||
BNJPHLCL_01802 | 0.0 | mrdA | 3.4.16.4 | M | penicillin-binding protein | |
BNJPHLCL_01803 | 1.1e-54 | yqzD | ||||
BNJPHLCL_01804 | 1.6e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
BNJPHLCL_01806 | 6.4e-202 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
BNJPHLCL_01807 | 2.8e-29 | yqgQ | S | protein conserved in bacteria | ||
BNJPHLCL_01808 | 1.6e-169 | glcK | 2.7.1.2 | G | Glucokinase | |
BNJPHLCL_01809 | 2.9e-21 | yqgW | S | Protein of unknown function (DUF2759) | ||
BNJPHLCL_01810 | 5e-124 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
BNJPHLCL_01811 | 5.7e-36 | yqgY | S | Protein of unknown function (DUF2626) | ||
BNJPHLCL_01812 | 1e-128 | K | Helix-turn-helix domain | |||
BNJPHLCL_01813 | 1.6e-202 | comGA | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
BNJPHLCL_01814 | 3.7e-171 | comGB | NU | COG1459 Type II secretory pathway, component PulF | ||
BNJPHLCL_01815 | 9.9e-49 | comGC | U | Required for transformation and DNA binding | ||
BNJPHLCL_01816 | 5.7e-74 | gspH | NU | COG2165 Type II secretory pathway, pseudopilin PulG | ||
BNJPHLCL_01818 | 2.9e-79 | comGF | U | COG4940 Competence protein ComGF | ||
BNJPHLCL_01819 | 7.6e-56 | S | ComG operon protein 7 | |||
BNJPHLCL_01820 | 3.8e-99 | aroK | 2.7.1.71, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
BNJPHLCL_01821 | 2.3e-10 | yqzE | S | YqzE-like protein | ||
BNJPHLCL_01822 | 2.7e-151 | yqhG | S | Bacterial protein YqhG of unknown function | ||
BNJPHLCL_01823 | 0.0 | yqhH | L | COG0553 Superfamily II DNA RNA helicases, SNF2 family | ||
BNJPHLCL_01824 | 5.4e-214 | gcvT | 1.4.4.2, 2.1.2.10 | E | The glycine cleavage system catalyzes the degradation of glycine | |
BNJPHLCL_01825 | 5.3e-256 | gcvPA | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
BNJPHLCL_01826 | 3.7e-287 | gcvPB | 1.4.4.2 | E | The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor | |
BNJPHLCL_01827 | 2.2e-66 | yqhL | P | COG0607 Rhodanese-related sulfurtransferase | ||
BNJPHLCL_01828 | 6.8e-161 | lipM | 6.3.1.20 | H | Catalyzes the transfer of endogenously produced octanoic acid from octanoyl-acyl-carrier-protein onto the lipoyl domain of GcvH, an intermediate carrier during protein lipoylation | |
BNJPHLCL_01829 | 0.0 | nrdA | 1.17.4.1 | F | Catalyzes the reduction of ribonucleotides to deoxyribonucleotides. May function to provide a pool of deoxyribonucleotide precursors for DNA repair during oxygen limitation and or for immediate growth after restoration of oxygen | |
BNJPHLCL_01830 | 2.3e-71 | bktB | 2.3.1.9 | I | Belongs to the thiolase family | |
BNJPHLCL_01831 | 5.8e-113 | yqhO | S | esterase of the alpha-beta hydrolase superfamily | ||
BNJPHLCL_01832 | 0.0 | pip | S | YhgE Pip N-terminal domain protein | ||
BNJPHLCL_01833 | 2.6e-97 | relA_2 | 2.7.6.5, 3.1.7.2 | KT | HD domain | |
BNJPHLCL_01834 | 1.8e-74 | yabE | S | 3D domain | ||
BNJPHLCL_01835 | 9.9e-177 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
BNJPHLCL_01837 | 0.0 | ppc | 4.1.1.31 | C | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
BNJPHLCL_01838 | 4.9e-187 | malR | K | Transcriptional regulator | ||
BNJPHLCL_01839 | 5.7e-261 | G | Major facilitator Superfamily | |||
BNJPHLCL_01840 | 0.0 | mapA | 2.4.1.8 | GH65 | G | Glycoside hydrolase, family 65 |
BNJPHLCL_01841 | 1.3e-125 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
BNJPHLCL_01842 | 3.2e-164 | lytR_1 | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
BNJPHLCL_01843 | 7.5e-123 | yhcW | 5.4.2.6 | S | hydrolase | |
BNJPHLCL_01844 | 4.6e-158 | cyoA | 1.10.3.10, 1.10.3.12 | C | Catalyzes quinol oxidation with the concomitant reduction of oxygen to water. Subunit II transfers the electrons from a quinol to the binuclear center of the catalytic subunit I | |
BNJPHLCL_01845 | 0.0 | qoxB | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
BNJPHLCL_01846 | 7.5e-109 | cyoC | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
BNJPHLCL_01847 | 3e-28 | qoxD | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
BNJPHLCL_01848 | 9.5e-29 | IQ | Short-chain dehydrogenase reductase sdr | |||
BNJPHLCL_01849 | 6e-146 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
BNJPHLCL_01850 | 2e-83 | |||||
BNJPHLCL_01851 | 5.4e-73 | 3.4.21.121 | O | Belongs to the peptidase S8 family | ||
BNJPHLCL_01852 | 0.0 | pmmB | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
BNJPHLCL_01853 | 1.3e-159 | yeaB | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
BNJPHLCL_01854 | 1.1e-175 | yhfP | 1.1.1.1 | C | Quinone oxidoreductase | |
BNJPHLCL_01855 | 9.7e-52 | S | Iron-sulphur cluster biosynthesis | |||
BNJPHLCL_01856 | 2.9e-136 | gumM | 2.4.1.187, 2.4.1.252 | GT26,GT4 | M | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
BNJPHLCL_01857 | 8e-129 | K | helix_turn_helix, arabinose operon control protein | |||
BNJPHLCL_01858 | 3.3e-228 | G | Bacterial extracellular solute-binding protein | |||
BNJPHLCL_01859 | 6.5e-221 | sugA | G | Binding-protein-dependent transport system inner membrane component | ||
BNJPHLCL_01860 | 9.4e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
BNJPHLCL_01861 | 0.0 | treP | 2.4.1.64 | GH65 | G | Glycoside hydrolase, family 65 |
BNJPHLCL_01862 | 6.7e-215 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
BNJPHLCL_01863 | 8.4e-219 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
BNJPHLCL_01864 | 2.5e-175 | kdsD | 5.3.1.13 | M | Belongs to the SIS family. GutQ KpsF subfamily | |
BNJPHLCL_01865 | 6.6e-156 | kdsA | 2.5.1.55 | M | Belongs to the KdsA family | |
BNJPHLCL_01866 | 0.0 | 2.7.1.202 | K | transcriptional regulator, MtlR | ||
BNJPHLCL_01867 | 1.2e-33 | L | Transposase DDE domain | |||
BNJPHLCL_01868 | 2.8e-84 | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | ||
BNJPHLCL_01870 | 1.4e-218 | S | Psort location CytoplasmicMembrane, score | |||
BNJPHLCL_01871 | 1.5e-120 | yfiR | K | Transcriptional regulator | ||
BNJPHLCL_01872 | 6.7e-145 | yfiS | EGP | Major facilitator Superfamily | ||
BNJPHLCL_01873 | 2.1e-54 | yfiS | EGP | Major facilitator Superfamily | ||
BNJPHLCL_01875 | 9.6e-138 | thiX | 2.7.1.50 | P | binding-protein-dependent transport systems inner membrane component | |
BNJPHLCL_01876 | 1.6e-177 | nrtA | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
BNJPHLCL_01878 | 2.3e-74 | S | Glyoxalase bleomycin resistance protein dioxygenase | |||
BNJPHLCL_01879 | 6.3e-139 | yitD | 4.4.1.19 | S | synthase | |
BNJPHLCL_01880 | 5.3e-127 | comB | 3.1.3.71 | H | Belongs to the ComB family | |
BNJPHLCL_01881 | 0.0 | cysJ | 1.8.1.2 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate. The flavoprotein component catalyzes the electron flow from NADPH - FAD - FMN to the hemoprotein component | |
BNJPHLCL_01882 | 0.0 | cysI | 1.7.7.1, 1.8.1.2, 1.8.7.1 | P | Component of the sulfite reductase complex that catalyzes the 6-electron reduction of sulfite to sulfide. This is one of several activities required for the biosynthesis of L- cysteine from sulfate | |
BNJPHLCL_01883 | 4.8e-108 | |||||
BNJPHLCL_01884 | 5.1e-65 | mta | K | transcriptional | ||
BNJPHLCL_01885 | 1.8e-38 | mta | K | transcriptional | ||
BNJPHLCL_01887 | 8e-268 | dapE | 3.5.1.16, 3.5.1.18 | E | Peptidase dimerisation domain | |
BNJPHLCL_01888 | 2.1e-177 | yjlA | EG | Putative multidrug resistance efflux transporter | ||
BNJPHLCL_01889 | 8.2e-190 | acoA | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | ||
BNJPHLCL_01890 | 1.5e-189 | acoB | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | ||
BNJPHLCL_01891 | 2e-214 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
BNJPHLCL_01892 | 4.9e-257 | acoL | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
BNJPHLCL_01893 | 0.0 | acoR | KQ | COG3284 Transcriptional activator of acetoin glycerol metabolism | ||
BNJPHLCL_01894 | 2.8e-180 | kefA | M | Mechanosensitive ion channel | ||
BNJPHLCL_01895 | 5.6e-191 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |||
BNJPHLCL_01896 | 1.2e-109 | nrdB | 1.17.4.1 | F | Ribonucleotide reductase, small chain | |
BNJPHLCL_01897 | 4e-104 | S | Appr-1'-p processing enzyme | |||
BNJPHLCL_01898 | 4.4e-25 | sspH | S | small acid-soluble spore protein | ||
BNJPHLCL_01899 | 2.7e-132 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BNJPHLCL_01900 | 3.2e-209 | 2.3.1.16, 2.3.1.9 | I | Belongs to the thiolase family | ||
BNJPHLCL_01901 | 3.3e-291 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
BNJPHLCL_01902 | 1.9e-62 | rtp | K | Plays a role in DNA replication and termination (fork arrest mechanism). Two dimers of rtp bind to the two inverted repeat regions (IRI and IRII) present in the termination site. The binding of each dimer is centered on an 8 bp direct repeat | ||
BNJPHLCL_01903 | 5.1e-142 | S | Sucrose-6F-phosphate phosphohydrolase | |||
BNJPHLCL_01904 | 5.4e-75 | ctsR | K | Belongs to the CtsR family | ||
BNJPHLCL_01905 | 1.3e-99 | mcsA | 2.7.14.1 | S | protein with conserved CXXC pairs | |
BNJPHLCL_01906 | 7.3e-192 | mcsB | 2.7.14.1, 2.7.3.2, 2.7.3.3 | E | Catalyzes the specific phosphorylation of arginine residues in a large number of proteins. Is part of the bacterial stress response system. Protein arginine phosphorylation has a physiologically important role and is involved in the regulation of many critical cellular processes, such as protein homeostasis, motility, competence, and stringent and stress responses, by regulating gene expression and protein activity | |
BNJPHLCL_01907 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
BNJPHLCL_01908 | 2.9e-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 | ||
BNJPHLCL_01909 | 6.9e-198 | yacL | S | COG4956 Integral membrane protein (PIN domain superfamily) | ||
BNJPHLCL_01910 | 2.6e-118 | ispD | 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
BNJPHLCL_01911 | 2.1e-82 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | I | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
BNJPHLCL_01912 | 1.9e-283 | 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) | |
BNJPHLCL_01913 | 7.7e-115 | cysE | 2.3.1.30 | E | Serine acetyltransferase | |
BNJPHLCL_01914 | 1.6e-271 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BNJPHLCL_01915 | 3e-69 | 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) | ||
BNJPHLCL_01916 | 8.2e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BNJPHLCL_01917 | 4.6e-69 | yacP | S | RNA-binding protein containing a PIN domain | ||
BNJPHLCL_01919 | 3.9e-147 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
BNJPHLCL_01921 | 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 | ||
BNJPHLCL_01922 | 6.8e-26 | yjzC | S | YjzC-like protein | ||
BNJPHLCL_01923 | 9.5e-52 | yitW | S | metal-sulfur cluster biosynthetic enzyme | ||
BNJPHLCL_01924 | 1.1e-155 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
BNJPHLCL_01925 | 6.3e-25 | S | Protein of unknown function (DUF3813) | |||
BNJPHLCL_01926 | 5.5e-158 | yitS | S | protein conserved in bacteria | ||
BNJPHLCL_01927 | 6.6e-104 | yisN | S | Protein of unknown function (DUF2777) | ||
BNJPHLCL_01928 | 3.3e-59 | yisL | S | UPF0344 protein | ||
BNJPHLCL_01929 | 2.3e-167 | yisK | Q | COG0179 2-keto-4-pentenoate hydratase 2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) | ||
BNJPHLCL_01930 | 6.4e-226 | P | Protein of unknown function (DUF418) | |||
BNJPHLCL_01931 | 3e-31 | gerPA | S | Spore germination protein | ||
BNJPHLCL_01932 | 8e-98 | gerPC | S | Spore germination protein | ||
BNJPHLCL_01933 | 2e-25 | gerPD | S | Spore germination protein | ||
BNJPHLCL_01934 | 8.4e-70 | gerPE | S | Spore germination protein GerPE | ||
BNJPHLCL_01935 | 4.7e-29 | gerPF | S | Spore germination protein gerPA/gerPF | ||
BNJPHLCL_01936 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BNJPHLCL_01937 | 0.0 | addB | 3.1.21.3, 3.6.4.12 | L | ATP-dependent helicase deoxyribonuclease subunit B | |
BNJPHLCL_01938 | 1.2e-143 | S | Mitochondrial biogenesis AIM24 | |||
BNJPHLCL_01939 | 8.2e-96 | comK | K | Competence transcription factor | ||
BNJPHLCL_01940 | 1.7e-08 | S | IDEAL | |||
BNJPHLCL_01941 | 2.2e-208 | yhfN | 3.4.24.84 | O | Peptidase M48 | |
BNJPHLCL_01942 | 5.7e-41 | azlD | S | branched-chain amino acid | ||
BNJPHLCL_01943 | 7.9e-118 | azlC | E | AzlC protein | ||
BNJPHLCL_01944 | 2.8e-293 | fadD | 6.2.1.3 | IQ | Activates fatty acids by binding to coenzyme A | |
BNJPHLCL_01945 | 3.2e-186 | lplJ | 6.3.1.20 | H | Lipoate-protein ligase | |
BNJPHLCL_01946 | 3e-21 | yhfH | S | YhfH-like protein | ||
BNJPHLCL_01947 | 4e-63 | ytkA | S | YtkA-like | ||
BNJPHLCL_01948 | 1.7e-102 | ypmQ | S | protein SCO1 SenC PrrC, involved in biogenesis of respiratory and photosynthetic systems | ||
BNJPHLCL_01949 | 5e-26 | aldA | 1.2.1.21, 1.2.1.22 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
BNJPHLCL_01950 | 4.1e-18 | aldA | 1.2.1.21, 1.2.1.22 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
BNJPHLCL_01951 | 2e-164 | EG | EamA-like transporter family | |||
BNJPHLCL_01952 | 5.1e-59 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_01953 | 1.7e-149 | yhgE | S | YhgE Pip N-terminal domain protein | ||
BNJPHLCL_01954 | 8.3e-102 | yhgD | K | Transcriptional regulator | ||
BNJPHLCL_01955 | 1.1e-267 | hemG | 1.14.19.9, 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
BNJPHLCL_01956 | 2.7e-182 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
BNJPHLCL_01957 | 4.3e-197 | hemE | 4.1.1.37 | H | Catalyzes the decarboxylation of four acetate groups of uroporphyrinogen-III to yield coproporphyrinogen-III | |
BNJPHLCL_01958 | 6.3e-93 | traP | 1.14.99.57 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
BNJPHLCL_01960 | 2.3e-238 | yhfA | C | membrane | ||
BNJPHLCL_01961 | 3.7e-229 | yhaA | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
BNJPHLCL_01962 | 7.2e-220 | ecsB | U | ABC transporter | ||
BNJPHLCL_01963 | 2.5e-138 | ecsA | V | transporter (ATP-binding protein) | ||
BNJPHLCL_01964 | 4.1e-74 | hit | FG | COG0537 Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
BNJPHLCL_01965 | 9.4e-84 | trpP | S | Tryptophan transporter TrpP | ||
BNJPHLCL_01966 | 2.1e-18 | yhaH | S | YtxH-like protein | ||
BNJPHLCL_01967 | 7.5e-103 | hpr | K | Negative regulator of protease production and sporulation | ||
BNJPHLCL_01968 | 1.1e-53 | yhaI | S | Protein of unknown function (DUF1878) | ||
BNJPHLCL_01971 | 6.2e-149 | prsA | 5.2.1.8 | M | plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
BNJPHLCL_01972 | 3e-27 | yhaL | S | Sporulation protein YhaL | ||
BNJPHLCL_01973 | 1.1e-178 | yhaM | L | Shows a 3'-5' exoribonuclease activity | ||
BNJPHLCL_01974 | 0.0 | L | AAA domain | |||
BNJPHLCL_01975 | 6.5e-248 | yhaO | L | DNA repair exonuclease | ||
BNJPHLCL_01976 | 5.3e-153 | ycgQ | S | membrane | ||
BNJPHLCL_01977 | 3.3e-145 | ycgR | S | permeases | ||
BNJPHLCL_01978 | 8.1e-121 | P | Integral membrane protein TerC family | |||
BNJPHLCL_01979 | 1.7e-27 | S | YhzD-like protein | |||
BNJPHLCL_01980 | 6.4e-137 | yhaR | 5.3.3.18 | I | enoyl-CoA hydratase | |
BNJPHLCL_01981 | 2.7e-160 | yhaX | S | hydrolases of the HAD superfamily | ||
BNJPHLCL_01982 | 3.9e-54 | yheA | S | Belongs to the UPF0342 family | ||
BNJPHLCL_01983 | 6.5e-207 | yheB | S | Belongs to the UPF0754 family | ||
BNJPHLCL_01984 | 7.8e-260 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
BNJPHLCL_01985 | 4.9e-212 | yheC | HJ | YheC/D like ATP-grasp | ||
BNJPHLCL_01987 | 1.7e-270 | gshB | 6.3.2.2, 6.3.2.3 | HJ | YheC/D like ATP-grasp | |
BNJPHLCL_01988 | 5.3e-228 | HJ | COG0189 Glutathione synthase Ribosomal protein S6 modification enzyme (glutaminyl transferase) | |||
BNJPHLCL_01989 | 3.4e-166 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
BNJPHLCL_01990 | 3.8e-204 | msmK | P | Belongs to the ABC transporter superfamily | ||
BNJPHLCL_01991 | 3.4e-29 | sspB | S | spore protein | ||
BNJPHLCL_01992 | 3.2e-264 | fumC | 1.1.1.38, 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
BNJPHLCL_01993 | 4.4e-18 | S | transposase or invertase | |||
BNJPHLCL_01994 | 1.3e-15 | S | transposase or invertase | |||
BNJPHLCL_01995 | 1.7e-147 | S | transposase or invertase | |||
BNJPHLCL_01997 | 8.3e-105 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
BNJPHLCL_01998 | 4.3e-40 | crh | G | Phosphocarrier protein Chr | ||
BNJPHLCL_01999 | 2e-172 | whiA | K | May be required for sporulation | ||
BNJPHLCL_02000 | 8.5e-179 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
BNJPHLCL_02001 | 1.8e-167 | rapZ | S | Displays ATPase and GTPase activities | ||
BNJPHLCL_02002 | 5.1e-86 | yvcI | 3.6.1.55 | F | Nudix hydrolase | |
BNJPHLCL_02003 | 3.1e-178 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
BNJPHLCL_02004 | 3.4e-251 | S | COG0457 FOG TPR repeat | |||
BNJPHLCL_02005 | 6.8e-71 | yvoF | S | COG0110 Acetyltransferase (isoleucine patch superfamily) | ||
BNJPHLCL_02006 | 2.8e-114 | ppaX | 3.1.3.18, 3.6.1.1 | S | Hydrolyzes pyrophosphate formed during P-Ser-HPr dephosphorylation by HPrK P. Might play a role in controlling the intracellular pyrophosphate pool | |
BNJPHLCL_02007 | 9.2e-155 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
BNJPHLCL_02008 | 2.8e-171 | 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. Also phosphorylates dephosphorylates the HPr-like catabolite repression protein crh on a specific serine residue. Therefore, by controlling the phosphorylation state of HPr and crh, 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 | ||
BNJPHLCL_02009 | 3.5e-31 | yvlD | S | Membrane | ||
BNJPHLCL_02010 | 4.4e-171 | yvlB | S | Putative adhesin | ||
BNJPHLCL_02011 | 1.4e-138 | M | Glycosyltransferase like family 2 | |||
BNJPHLCL_02012 | 4.9e-108 | tagG | GM | Transport permease protein | ||
BNJPHLCL_02013 | 4.1e-194 | tagF | 2.7.8.12 | M | glycosyl glycerophosphate transferases involved in teichoic acid biosynthesis TagF TagB EpsJ RodC | |
BNJPHLCL_02014 | 1.1e-121 | K | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | |||
BNJPHLCL_02015 | 1.5e-212 | dctA | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
BNJPHLCL_02016 | 0.0 | glpD | 1.1.5.3 | C | Belongs to the FAD-dependent glycerol-3-phosphate dehydrogenase family | |
BNJPHLCL_02017 | 5.8e-288 | glpK | 2.7.1.30 | C | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
BNJPHLCL_02018 | 4.1e-147 | glpF | G | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
BNJPHLCL_02019 | 3.8e-99 | 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 | ||
BNJPHLCL_02021 | 7.8e-41 | fer | C | Ferredoxin | ||
BNJPHLCL_02022 | 1.1e-96 | fmnP | 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 | ||
BNJPHLCL_02023 | 4.8e-115 | M | COG0739 Membrane proteins related to metalloendopeptidases | |||
BNJPHLCL_02024 | 0.0 | resE | 2.7.13.3 | T | Histidine kinase | |
BNJPHLCL_02025 | 3.3e-132 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNJPHLCL_02026 | 2.2e-229 | ccsA | O | 'COG0755 ABC-type transport system involved in cytochrome c biogenesis, permease component' | ||
BNJPHLCL_02027 | 0.0 | ccs1 | O | COG1333 ResB protein required for cytochrome c biosynthesis | ||
BNJPHLCL_02028 | 2.8e-99 | resA | CO | Thiol-disulfide oxidoreductase which is required in disulfide reduction during c-type cytochrome synthesis. May accept reducing equivalents from CcdA, leading to breakage of disulfide bonds in apocytochrome c | ||
BNJPHLCL_02029 | 1.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
BNJPHLCL_02030 | 1.4e-87 | spmB | S | Spore maturation protein | ||
BNJPHLCL_02031 | 5.2e-96 | spmA | S | Spore maturation protein | ||
BNJPHLCL_02032 | 8.1e-202 | dacB | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNJPHLCL_02033 | 1.2e-106 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
BNJPHLCL_02034 | 1.7e-131 | 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 | ||
BNJPHLCL_02036 | 2.2e-60 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
BNJPHLCL_02037 | 1.6e-250 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
BNJPHLCL_02038 | 2.3e-268 | spoVAF | EG | Stage V sporulation protein AF | ||
BNJPHLCL_02039 | 8e-105 | spoVAEA | S | Stage V sporulation protein AE | ||
BNJPHLCL_02040 | 4.6e-65 | spoVAB | S | Stage V sporulation protein AB | ||
BNJPHLCL_02041 | 6.5e-108 | spoVAA | S | Stage V sporulation protein AA | ||
BNJPHLCL_02042 | 1.4e-133 | sigF | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
BNJPHLCL_02043 | 1.8e-75 | spoIIAB | 2.7.11.1 | F | Binds to sigma F and blocks its ability to form an RNA polymerase holoenzyme (E-sigma F). Phosphorylates SpoIIAA on a serine residue. This phosphorylation may enable SpoIIAA to act as an anti-anti-sigma factor that counteracts SpoIIAB and thus releases sigma F from inhibition | |
BNJPHLCL_02044 | 2.5e-56 | spoIIAA | T | Belongs to the anti-sigma-factor antagonist family | ||
BNJPHLCL_02045 | 7.6e-211 | dacF | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNJPHLCL_02047 | 3.6e-168 | xerD | L | recombinase XerD | ||
BNJPHLCL_02048 | 6.3e-34 | S | Protein of unknown function (DUF4227) | |||
BNJPHLCL_02049 | 3.5e-85 | fur | P | Belongs to the Fur family | ||
BNJPHLCL_02050 | 1.5e-104 | spoIIM | S | Required for complete septum migration and engulfment of the forespore compartment during sporulation. Required for stabilizing and recruiting of SpoIIP to the septal membrane | ||
BNJPHLCL_02051 | 1.1e-228 | yqxK | 3.6.4.12 | L | DNA helicase | |
BNJPHLCL_02052 | 1.6e-97 | nudF | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | |
BNJPHLCL_02054 | 1.4e-167 | yqkF | C | oxidoreductases (related to aryl-alcohol dehydrogenases) | ||
BNJPHLCL_02055 | 1.6e-09 | S | Protein of unknown function (DUF3886) | |||
BNJPHLCL_02056 | 5.6e-110 | xpaC | S | 5-bromo-4-chloroindolyl phosphate hydrolysis protein | ||
BNJPHLCL_02057 | 1.3e-213 | yaaN | P | Belongs to the TelA family | ||
BNJPHLCL_02058 | 8.2e-176 | yqkD | S | COG1073 Hydrolases of the alpha beta superfamily | ||
BNJPHLCL_02059 | 2.4e-235 | yaaH_2 | M | Glycoside Hydrolase Family | ||
BNJPHLCL_02060 | 6.6e-54 | S | YolD-like protein | |||
BNJPHLCL_02061 | 1.3e-240 | polYB | 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 | |
BNJPHLCL_02062 | 8.5e-145 | yqjQ | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
BNJPHLCL_02063 | 6.3e-143 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BNJPHLCL_02064 | 6.5e-173 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
BNJPHLCL_02065 | 1.7e-292 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
BNJPHLCL_02066 | 1.1e-225 | 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 | |
BNJPHLCL_02067 | 2.9e-76 | cheW | NT | COG0835 Chemotaxis signal transduction protein | ||
BNJPHLCL_02068 | 2.1e-202 | yqjE | 3.4.11.4 | E | COG2195 Di- and tripeptidases | |
BNJPHLCL_02069 | 9.1e-301 | msbA2 | 3.6.3.44 | V | ABC transporter | |
BNJPHLCL_02070 | 3.2e-113 | yhhQ_2 | S | Involved in the import of queuosine (Q) precursors, required for Q precursor salvage | ||
BNJPHLCL_02071 | 2.9e-98 | queF | 1.7.1.13 | S | Catalyzes the NADPH-dependent reduction of 7-cyano-7- deazaguanine (preQ0) to 7-aminomethyl-7-deazaguanine (preQ1) | |
BNJPHLCL_02072 | 7.7e-104 | S | MMPL domain protein | |||
BNJPHLCL_02073 | 1.5e-264 | S | MMPL domain protein | |||
BNJPHLCL_02074 | 1.4e-299 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
BNJPHLCL_02075 | 2.4e-43 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
BNJPHLCL_02076 | 1.2e-143 | T | COG1366 Anti-anti-sigma regulatory factor (antagonist of anti-sigma factor) | |||
BNJPHLCL_02077 | 1.8e-136 | sigG | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
BNJPHLCL_02078 | 3.5e-113 | sigE | K | sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
BNJPHLCL_02079 | 1.2e-163 | spoIIGA | M | aspartic protease that is responsible for the proteolytic cleavage of the RNA polymerase sigma E factor (SigE spoIIGB) to yield the active peptide in the mother cell during sporulation. Responds to a signal from the forespore that is triggered by the extracellular signal protein SpoIIR | ||
BNJPHLCL_02080 | 3.6e-189 | 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 | ||
BNJPHLCL_02081 | 6.4e-219 | 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 | ||
BNJPHLCL_02082 | 1.1e-117 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
BNJPHLCL_02083 | 1.1e-203 | 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) |
BNJPHLCL_02084 | 7.7e-189 | spoVE | D | Belongs to the SEDS family | ||
BNJPHLCL_02085 | 1.3e-257 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
BNJPHLCL_02086 | 2.5e-170 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
BNJPHLCL_02087 | 4.9e-78 | murF | 6.3.2.10 | M | UDP-N-acetylmuramoyl-tripeptide-D-alanyl-D-alanine ligase activity | |
BNJPHLCL_02088 | 4.8e-279 | murE | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
BNJPHLCL_02089 | 0.0 | ftsI | 3.4.16.4 | M | stage V sporulation protein D | |
BNJPHLCL_02090 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
BNJPHLCL_02091 | 1.7e-39 | ftsL | D | Essential cell division protein | ||
BNJPHLCL_02092 | 6.6e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
BNJPHLCL_02093 | 1.4e-77 | mraZ | K | Belongs to the MraZ family | ||
BNJPHLCL_02094 | 0.0 | bshC | S | Involved in bacillithiol (BSH) biosynthesis. May catalyze the last step of the pathway, the addition of cysteine to glucosamine malate (GlcN-Mal) to generate BSH | ||
BNJPHLCL_02095 | 3e-159 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
BNJPHLCL_02096 | 2.3e-92 | ylbP | K | n-acetyltransferase | ||
BNJPHLCL_02097 | 1.6e-80 | rsfA | S | SANT SWI3, ADA2, N-CoR and TFIIIB'' DNA-binding domains | ||
BNJPHLCL_02098 | 1.1e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
BNJPHLCL_02099 | 1.2e-93 | yceD | S | metal-binding, possibly nucleic acid-binding protein | ||
BNJPHLCL_02100 | 6.3e-224 | ylbM | S | Belongs to the UPF0348 family | ||
BNJPHLCL_02101 | 6.5e-193 | ylbL | T | Belongs to the peptidase S16 family | ||
BNJPHLCL_02102 | 7.6e-138 | ylbK | S | esterase of the alpha-beta hydrolase superfamily | ||
BNJPHLCL_02103 | 5.5e-220 | ylbJ | S | Sporulation integral membrane protein YlbJ | ||
BNJPHLCL_02104 | 6.6e-84 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
BNJPHLCL_02105 | 2.3e-105 | rsmD | 2.1.1.171 | L | Methyltransferase | |
BNJPHLCL_02106 | 7.7e-67 | S | Methylthioribose kinase | |||
BNJPHLCL_02107 | 4.1e-45 | ylbG | S | UPF0298 protein | ||
BNJPHLCL_02108 | 2.8e-73 | ylbF | S | Belongs to the UPF0342 family | ||
BNJPHLCL_02109 | 1.9e-62 | |||||
BNJPHLCL_02110 | 7.9e-38 | ylbE | S | YlbE-like protein | ||
BNJPHLCL_02111 | 2e-70 | ylbD | S | Putative coat protein | ||
BNJPHLCL_02112 | 1.7e-84 | yiiD | Q | protein, possibly involved in aromatic compounds catabolism | ||
BNJPHLCL_02113 | 3.9e-167 | ylbC | S | protein with SCP PR1 domains | ||
BNJPHLCL_02114 | 9.6e-64 | ylbA | S | YugN-like family | ||
BNJPHLCL_02115 | 1.7e-168 | ctaG | S | cytochrome c oxidase | ||
BNJPHLCL_02116 | 9.2e-53 | ctaF | 1.10.3.12, 1.9.3.1 | C | COG3125 Heme copper-type cytochrome quinol oxidase, subunit 4 | |
BNJPHLCL_02117 | 2.1e-114 | cyoC | 1.10.3.12, 1.9.3.1 | C | COG1845 Heme copper-type cytochrome quinol oxidase, subunit 3 | |
BNJPHLCL_02118 | 0.0 | ctaD | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
BNJPHLCL_02119 | 4.9e-196 | ctaC | 1.9.3.1 | C | Subunits I and II form the functional core of the enzyme complex. Electrons originating in cytochrome c are transferred via heme a and Cu(A) to the binuclear center formed by heme a3 and Cu(B) | |
BNJPHLCL_02120 | 1.6e-163 | ctaB | 2.5.1.141 | O | Converts heme B (protoheme IX) to heme O by substitution of the vinyl group on carbon 2 of heme B porphyrin ring with a hydroxyethyl farnesyl side group | |
BNJPHLCL_02121 | 1.2e-174 | ctaA | 2.5.1.141 | O | Catalyzes the oxidation of the C8 methyl side group on heme O porphyrin ring into a formyl group | |
BNJPHLCL_02122 | 4.4e-217 | ftsW | D | Belongs to the SEDS family | ||
BNJPHLCL_02123 | 1.5e-43 | ylaN | S | Belongs to the UPF0358 family | ||
BNJPHLCL_02124 | 9.1e-89 | ylaL | S | Part of the MsrPQ system that repairs oxidized periplasmic proteins containing methionine sulfoxide residues (Met-O), using respiratory chain electrons. Thus protects these proteins from oxidative-stress damage caused by reactive species of oxygen and chlorine generated by the host defense mechanisms. MsrPQ is essential for the maintenance of envelope integrity under bleach stress, rescuing a wide series of structurally unrelated periplasmic proteins from methionine oxidation. The catalytic subunit MsrP is non-stereospecific, being able to reduce both (R-) and (S-) diastereoisomers of methionine sulfoxide | ||
BNJPHLCL_02125 | 2.6e-247 | phoH | T | ATPase related to phosphate starvation-inducible protein PhoH | ||
BNJPHLCL_02126 | 2.1e-52 | ylaH | S | YlaH-like protein | ||
BNJPHLCL_02127 | 0.0 | typA | T | GTP-binding protein TypA | ||
BNJPHLCL_02128 | 6e-25 | S | Family of unknown function (DUF5325) | |||
BNJPHLCL_02129 | 8.7e-150 | suhB | 3.1.3.25 | G | Inositol monophosphatase | |
BNJPHLCL_02130 | 4e-24 | |||||
BNJPHLCL_02131 | 3.6e-119 | yktB | S | Belongs to the UPF0637 family | ||
BNJPHLCL_02132 | 4.5e-48 | yktA | S | Belongs to the UPF0223 family | ||
BNJPHLCL_02133 | 9.4e-275 | speA | 4.1.1.19 | E | Arginine | |
BNJPHLCL_02135 | 2.3e-32 | |||||
BNJPHLCL_02136 | 4.8e-260 | lpdA | 1.8.1.4 | C | COG1249 Pyruvate 2-oxoglutarate dehydrogenase complex, dihydrolipoamide dehydrogenase (E3) component, and related enzymes | |
BNJPHLCL_02137 | 3.7e-230 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
BNJPHLCL_02138 | 1e-179 | pdhB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
BNJPHLCL_02139 | 7.3e-203 | pdhA | 1.2.4.1, 1.2.4.4 | C | COG1071 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, alpha subunit | |
BNJPHLCL_02140 | 1.2e-29 | ykzG | S | Belongs to the UPF0356 family | ||
BNJPHLCL_02141 | 0.0 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
BNJPHLCL_02142 | 1.8e-18 | S | YhfH-like protein | |||
BNJPHLCL_02143 | 3.6e-218 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
BNJPHLCL_02144 | 1.2e-70 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
BNJPHLCL_02145 | 1.9e-155 | ccpC | K | Transcriptional regulator | ||
BNJPHLCL_02146 | 6.5e-78 | ykuL | S | CBS domain | ||
BNJPHLCL_02147 | 5.8e-39 | ykuJ | S | protein conserved in bacteria | ||
BNJPHLCL_02148 | 6.7e-162 | 3.5.1.4 | C | Acetamidase | ||
BNJPHLCL_02149 | 9.3e-141 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_02150 | 1e-31 | |||||
BNJPHLCL_02151 | 1e-32 | T | Diguanylate cyclase | |||
BNJPHLCL_02152 | 3e-16 | T | Diguanylate cyclase | |||
BNJPHLCL_02153 | 0.0 | ydgH | S | drug exporters of the RND superfamily | ||
BNJPHLCL_02154 | 2.6e-85 | ykyB | S | YkyB-like protein | ||
BNJPHLCL_02155 | 6.4e-165 | cheV | 2.7.13.3 | T | Chemotaxis protein CheV | |
BNJPHLCL_02156 | 4.4e-219 | patA | 2.6.1.1 | E | Aminotransferase | |
BNJPHLCL_02157 | 5e-159 | glxR | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | |
BNJPHLCL_02158 | 1.1e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_02159 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
BNJPHLCL_02160 | 3.2e-40 | ptsH | G | phosphocarrier protein HPr | ||
BNJPHLCL_02161 | 5e-26 | |||||
BNJPHLCL_02162 | 4.2e-26 | ykvS | S | protein conserved in bacteria | ||
BNJPHLCL_02163 | 7.3e-104 | S | Abortive infection protein | |||
BNJPHLCL_02164 | 1.1e-179 | ykvI | S | membrane | ||
BNJPHLCL_02165 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
BNJPHLCL_02167 | 4.3e-71 | XK27_09985 | S | Protein of unknown function (DUF1232) | ||
BNJPHLCL_02168 | 4e-78 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
BNJPHLCL_02169 | 7.7e-288 | kinE | 2.7.13.3 | T | Histidine kinase | |
BNJPHLCL_02171 | 4.3e-19 | S | Stage 0 Sporulation Regulatory protein | |||
BNJPHLCL_02172 | 8.1e-28 | sspD | S | small acid-soluble spore protein | ||
BNJPHLCL_02173 | 2.1e-127 | ykoY | P | COG0861 Membrane protein TerC, possibly involved in tellurium resistance | ||
BNJPHLCL_02174 | 6.7e-81 | |||||
BNJPHLCL_02175 | 4.3e-302 | 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 | ||
BNJPHLCL_02176 | 1.1e-206 | kinC | 2.7.13.3 | T | COG0642 Signal transduction histidine kinase | |
BNJPHLCL_02177 | 2.6e-180 | mocA | S | Oxidoreductase | ||
BNJPHLCL_02178 | 4e-75 | dps | P | Ferritin-like domain | ||
BNJPHLCL_02179 | 1.6e-124 | S | membrane transporter protein | |||
BNJPHLCL_02180 | 9e-231 | hmp | 1.14.12.17 | C | Is involved in NO detoxification in an aerobic process, termed nitric oxide dioxygenase (NOD) reaction that utilizes O(2) and NAD(P)H to convert NO to nitrate, which protects the bacterium from various noxious nitrogen compounds. Therefore, plays a central role in the inducible response to nitrosative stress | |
BNJPHLCL_02181 | 3.9e-75 | nsrR | K | Transcriptional regulator | ||
BNJPHLCL_02182 | 6.4e-142 | tesE | Q | COG3971 2-keto-4-pentenoate hydratase | ||
BNJPHLCL_02183 | 3.1e-246 | proP | EGP | Transporter | ||
BNJPHLCL_02184 | 2.6e-175 | ldhA | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
BNJPHLCL_02186 | 4.9e-129 | |||||
BNJPHLCL_02187 | 3.7e-45 | |||||
BNJPHLCL_02188 | 1.7e-143 | S | Protein of unknown function (DUF1672) | |||
BNJPHLCL_02189 | 7.9e-100 | bioY | S | Biotin biosynthesis protein | ||
BNJPHLCL_02190 | 5e-139 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
BNJPHLCL_02191 | 3.6e-76 | lytE | CBM50 | M | COG0791 Cell wall-associated hydrolases (invasion-associated proteins) | |
BNJPHLCL_02192 | 3.2e-76 | |||||
BNJPHLCL_02193 | 3.6e-197 | yfmL | 3.6.4.13 | L | COG0513 Superfamily II DNA and RNA helicases | |
BNJPHLCL_02194 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BNJPHLCL_02195 | 1.3e-171 | corA | P | Mg2 transporter protein CorA family protein | ||
BNJPHLCL_02198 | 8e-234 | panF | H | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
BNJPHLCL_02199 | 9.6e-48 | yhdT | S | Sodium pantothenate symporter | ||
BNJPHLCL_02200 | 9.1e-164 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
BNJPHLCL_02201 | 1.7e-284 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This 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 | |
BNJPHLCL_02202 | 3e-16 | S | Protein of unknown function (DUF4064) | |||
BNJPHLCL_02203 | 4.2e-149 | 3.5.3.1, 3.5.3.11 | E | Belongs to the arginase family | ||
BNJPHLCL_02204 | 5.4e-242 | hom | 1.1.1.3 | E | homoserine dehydrogenase | |
BNJPHLCL_02205 | 5.2e-190 | thrC | 4.2.3.1 | E | Catalyzes the gamma-elimination of phosphate from L- phosphohomoserine and the beta-addition of water to produce L- threonine | |
BNJPHLCL_02206 | 3.1e-159 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
BNJPHLCL_02207 | 2.6e-135 | P | ABC transporter, ATP-binding protein | |||
BNJPHLCL_02208 | 9.8e-183 | M1-596 | P | COG0715 ABC-type nitrate sulfonate bicarbonate transport systems, periplasmic components | ||
BNJPHLCL_02209 | 3.2e-136 | ssuC_1 | P | binding-protein-dependent transport systems inner membrane component | ||
BNJPHLCL_02210 | 1.4e-50 | M1-594 | S | Thiamine-binding protein | ||
BNJPHLCL_02211 | 6.9e-265 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
BNJPHLCL_02212 | 2.7e-85 | S | Heat induced stress protein YflT | |||
BNJPHLCL_02213 | 1.5e-161 | prpB | 4.1.3.30 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
BNJPHLCL_02214 | 2.9e-276 | prpD | 4.2.1.79 | S | 2-methylcitrate dehydratase | |
BNJPHLCL_02215 | 7.8e-213 | prpC | 2.3.3.1, 2.3.3.5 | C | Belongs to the citrate synthase family | |
BNJPHLCL_02216 | 2.9e-63 | manO | S | Domain of unknown function (DUF956) | ||
BNJPHLCL_02217 | 4.8e-168 | manN | G | COG3716 Phosphotransferase system, mannose fructose N-acetylgalactosamine-specific component IID | ||
BNJPHLCL_02218 | 1.5e-117 | manY | G | COG3715 Phosphotransferase system, mannose fructose N-acetylgalactosamine-specific component IIC | ||
BNJPHLCL_02219 | 6e-177 | manL | 2.7.1.191 | G | PTS system mannose fructose sorbose family | |
BNJPHLCL_02220 | 2e-83 | manX | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
BNJPHLCL_02221 | 0.0 | levR | K | PTS system fructose IIA component | ||
BNJPHLCL_02222 | 0.0 | S | ATPase. Has a role at an early stage in the morphogenesis of the spore coat | |||
BNJPHLCL_02223 | 2.9e-201 | pgl | 3.1.1.31 | G | 6-phosphogluconolactonase | |
BNJPHLCL_02224 | 2.9e-48 | yqgV | S | Thiamine-binding protein | ||
BNJPHLCL_02225 | 2.8e-238 | cshA | L | COG2256 ATPase related to the helicase subunit of the Holliday junction resolvase | ||
BNJPHLCL_02226 | 4.1e-136 | yrvM | H | COG1179 Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 1 | ||
BNJPHLCL_02227 | 6.5e-163 | ybaS | 1.1.1.58 | S | Na -dependent transporter | |
BNJPHLCL_02229 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
BNJPHLCL_02230 | 7.8e-249 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
BNJPHLCL_02232 | 1.8e-273 | lytH | 3.5.1.28, 6.1.1.12 | M | COG3103 SH3 domain protein | |
BNJPHLCL_02233 | 5.2e-307 | yhcA5 | EGP | Major facilitator Superfamily | ||
BNJPHLCL_02234 | 1.4e-105 | emrA | V | COG1566 Multidrug resistance efflux pump | ||
BNJPHLCL_02235 | 1.6e-68 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BNJPHLCL_02236 | 1.8e-75 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
BNJPHLCL_02237 | 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 | |
BNJPHLCL_02238 | 5.3e-95 | 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 | |
BNJPHLCL_02239 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
BNJPHLCL_02240 | 0.0 | secF | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. SecDF uses the proton motive force (PMF) to complete protein translocation after the ATP-dependent function of SecA | ||
BNJPHLCL_02241 | 3.6e-60 | yrzD | S | Post-transcriptional regulator | ||
BNJPHLCL_02242 | 1.9e-270 | spoVB | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
BNJPHLCL_02243 | 6e-104 | yrbG | S | membrane | ||
BNJPHLCL_02244 | 4.9e-61 | yrzE | S | Protein of unknown function (DUF3792) | ||
BNJPHLCL_02245 | 1.2e-44 | yajC | U | Preprotein translocase subunit YajC | ||
BNJPHLCL_02246 | 6.9e-225 | 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) | |
BNJPHLCL_02247 | 1.1e-192 | 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) | |
BNJPHLCL_02248 | 5.4e-27 | yrzS | S | Protein of unknown function (DUF2905) | ||
BNJPHLCL_02249 | 2.3e-184 | 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 | |
BNJPHLCL_02250 | 1.7e-105 | 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 | |
BNJPHLCL_02251 | 1.7e-128 | yebC | K | transcriptional regulatory protein | ||
BNJPHLCL_02252 | 2.3e-189 | 1.1.1.34, 2.7.1.89 | M | choline kinase involved in LPS biosynthesis | ||
BNJPHLCL_02253 | 3.4e-140 | safA | M | spore coat assembly protein SafA | ||
BNJPHLCL_02254 | 3.5e-97 | niaR | S | small molecule binding protein (contains 3H domain) | ||
BNJPHLCL_02255 | 7.8e-157 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
BNJPHLCL_02256 | 1.2e-74 | pheB | 5.4.99.5 | S | Belongs to the UPF0735 family | |
BNJPHLCL_02257 | 3.4e-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 | ||
BNJPHLCL_02258 | 7.5e-97 | spo0B | T | Sporulation initiation phospho-transferase B, C-terminal | ||
BNJPHLCL_02259 | 1.1e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
BNJPHLCL_02260 | 4.6e-52 | ysxB | J | ribosomal protein | ||
BNJPHLCL_02261 | 1.7e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
BNJPHLCL_02262 | 1.8e-260 | rng | J | ribonuclease, Rne Rng family | ||
BNJPHLCL_02263 | 4.3e-158 | spoIVFB | S | Stage IV sporulation protein | ||
BNJPHLCL_02264 | 1.4e-133 | spoIVFA | M | COG0739 Membrane proteins related to metalloendopeptidases | ||
BNJPHLCL_02265 | 2.5e-144 | minD | D | Belongs to the ParA family | ||
BNJPHLCL_02266 | 1.4e-119 | 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 | ||
BNJPHLCL_02267 | 9e-87 | mreD | M | shape-determining protein | ||
BNJPHLCL_02268 | 5.3e-140 | mreC | M | Involved in formation and maintenance of cell shape | ||
BNJPHLCL_02269 | 1.1e-184 | mreB | D | Rod shape-determining protein MreB | ||
BNJPHLCL_02271 | 1.8e-17 | gerLA | EG | Spore germination protein | ||
BNJPHLCL_02272 | 1.7e-72 | S | membrane transporter protein | |||
BNJPHLCL_02273 | 2.5e-25 | yrkI | O | Sulfurtransferase TusA | ||
BNJPHLCL_02274 | 6.2e-157 | yrkH | P | COG0607 Rhodanese-related sulfurtransferase | ||
BNJPHLCL_02275 | 2.1e-56 | S | DsrE/DsrF-like family | |||
BNJPHLCL_02276 | 1.7e-67 | yrkF | OP | Belongs to the sulfur carrier protein TusA family | ||
BNJPHLCL_02277 | 3.2e-26 | P | Sulfurtransferase | |||
BNJPHLCL_02278 | 2.1e-28 | yrkD | S | Metal-sensitive transcriptional repressor | ||
BNJPHLCL_02279 | 5.2e-39 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
BNJPHLCL_02280 | 4.4e-42 | Q | ubiE/COQ5 methyltransferase family | |||
BNJPHLCL_02281 | 1.2e-15 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |||
BNJPHLCL_02282 | 9.4e-29 | CO | Thioredoxin-like | |||
BNJPHLCL_02283 | 1.2e-33 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
BNJPHLCL_02284 | 1.9e-84 | ccdA | O | Cytochrome C biogenesis protein transmembrane region | ||
BNJPHLCL_02285 | 4.9e-29 | O | OsmC-like protein | |||
BNJPHLCL_02286 | 5.9e-47 | T | Transcriptional regulatory protein, C terminal | |||
BNJPHLCL_02287 | 8.9e-48 | L | crispr-associated protein | |||
BNJPHLCL_02288 | 2.9e-08 | |||||
BNJPHLCL_02289 | 6.5e-11 | S | Pfam:DUF2276 | |||
BNJPHLCL_02290 | 4.4e-13 | cysH | 1.8.4.10, 1.8.4.8 | EH | Belongs to the PAPS reductase family. CysH subfamily | |
BNJPHLCL_02292 | 1.5e-14 | |||||
BNJPHLCL_02293 | 5.1e-32 | S | Cold-inducible protein YdjO | |||
BNJPHLCL_02295 | 3.7e-182 | K | Transcriptional regulator | |||
BNJPHLCL_02296 | 4.1e-200 | galM | 2.7.1.6, 5.1.3.3 | G | Converts alpha-aldose to the beta-anomer | |
BNJPHLCL_02297 | 8.3e-279 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
BNJPHLCL_02298 | 1.8e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
BNJPHLCL_02299 | 4.2e-225 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
BNJPHLCL_02300 | 2.5e-35 | K | ArsR family transcriptional regulator | |||
BNJPHLCL_02301 | 1.7e-210 | ydbM | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
BNJPHLCL_02304 | 3.2e-141 | hel | M | 5'-nucleotidase, lipoprotein e(P4) | ||
BNJPHLCL_02305 | 2e-40 | yjhE | S | Phage tail protein | ||
BNJPHLCL_02306 | 1.1e-84 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
BNJPHLCL_02307 | 1.8e-158 | 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 | |
BNJPHLCL_02308 | 1.2e-166 | yfhF | S | nucleoside-diphosphate sugar epimerase | ||
BNJPHLCL_02309 | 3.6e-210 | M | Glycosyl hydrolases family 25 | |||
BNJPHLCL_02310 | 4.4e-146 | ubiE | Q | Methyltransferase type 11 | ||
BNJPHLCL_02311 | 2.4e-71 | arsC | 1.20.4.1 | T | Low molecular weight phosphotyrosine protein phosphatase | |
BNJPHLCL_02312 | 8e-191 | arsB | P | Arsenic resistance protein | ||
BNJPHLCL_02313 | 1.2e-97 | padR | K | Domain of unknown function (DUF2703) | ||
BNJPHLCL_02314 | 0.0 | arsA | 3.6.3.16 | D | Anion-transporting ATPase | |
BNJPHLCL_02315 | 4.7e-54 | arsD | S | Arsenical resistance operon trans-acting repressor ArsD | ||
BNJPHLCL_02316 | 3.3e-58 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BNJPHLCL_02317 | 1.5e-231 | L | PFAM Transposase, IS4-like | |||
BNJPHLCL_02318 | 3.9e-206 | S | Phosphotransferase enzyme family | |||
BNJPHLCL_02319 | 4.6e-70 | S | Thioesterase-like superfamily | |||
BNJPHLCL_02320 | 1.2e-97 | K | Transcriptional regulator | |||
BNJPHLCL_02321 | 3.3e-109 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
BNJPHLCL_02322 | 6.1e-134 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
BNJPHLCL_02323 | 2.1e-28 | 6.2.1.3 | IQ | COG0318 Acyl-CoA synthetases (AMP-forming) AMP-acid ligases II | ||
BNJPHLCL_02324 | 2.3e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_02325 | 1.9e-236 | MA20_26760 | 1.3.8.7 | I | COG1960 Acyl-CoA dehydrogenases | |
BNJPHLCL_02326 | 1.4e-187 | T | Anti-anti-sigma regulatory factor (Antagonist of anti-sigma factor) | |||
BNJPHLCL_02327 | 3.2e-127 | yeeN | K | transcriptional regulatory protein | ||
BNJPHLCL_02328 | 3.2e-98 | |||||
BNJPHLCL_02329 | 3.7e-94 | |||||
BNJPHLCL_02330 | 2.8e-196 | ycgT | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
BNJPHLCL_02331 | 1.4e-150 | fhuC | 3.6.3.34 | HP | ABC transporter | |
BNJPHLCL_02332 | 2.9e-171 | fhuD | P | Periplasmic binding protein | ||
BNJPHLCL_02333 | 3.7e-180 | fhuB | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
BNJPHLCL_02334 | 1.3e-174 | fhuG | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
BNJPHLCL_02335 | 4.1e-136 | yfcA | S | membrane transporter protein | ||
BNJPHLCL_02336 | 1.1e-53 | ykkC | P | Multidrug resistance protein | ||
BNJPHLCL_02337 | 5e-48 | sugE | P | Multidrug resistance protein | ||
BNJPHLCL_02338 | 1e-92 | Q | Thioesterase superfamily | |||
BNJPHLCL_02339 | 4.8e-20 | S | transposase or invertase | |||
BNJPHLCL_02340 | 6.9e-206 | crtQ | M | Glycosyl transferase family 21 | ||
BNJPHLCL_02341 | 3.6e-103 | plsY | 2.3.1.15 | I | Belongs to the PlsY family | |
BNJPHLCL_02342 | 4.9e-193 | nrdB | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BNJPHLCL_02343 | 5.6e-88 | fld | C | Flavodoxin | ||
BNJPHLCL_02344 | 0.0 | nrdA | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BNJPHLCL_02346 | 5.6e-40 | |||||
BNJPHLCL_02347 | 1.3e-29 | P | Heavy-metal-associated domain | |||
BNJPHLCL_02348 | 0.0 | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | ||
BNJPHLCL_02349 | 2.1e-137 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | T | COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
BNJPHLCL_02350 | 1.9e-200 | 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 | ||
BNJPHLCL_02351 | 6.5e-81 | fld | C | Flavodoxin | ||
BNJPHLCL_02353 | 4.9e-173 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase | |
BNJPHLCL_02354 | 5e-125 | gntR | K | transcriptional | ||
BNJPHLCL_02355 | 2.9e-306 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
BNJPHLCL_02356 | 1.7e-230 | EG | COG2610 H gluconate symporter and related permeases | |||
BNJPHLCL_02357 | 7.4e-132 | treR | K | transcriptional | ||
BNJPHLCL_02358 | 0.0 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
BNJPHLCL_02359 | 6.5e-265 | treP | 2.7.1.201, 2.7.1.211 | G | phosphotransferase system | |
BNJPHLCL_02360 | 1.1e-81 | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | ||
BNJPHLCL_02361 | 8.9e-268 | proWX | EM | COG1174 ABC-type proline glycine betaine transport systems, permease component | ||
BNJPHLCL_02362 | 7e-178 | proV | E | COG1125 ABC-type proline glycine betaine transport systems, ATPase components | ||
BNJPHLCL_02363 | 1.4e-181 | ghrB | 1.1.1.215, 1.1.1.26, 1.1.1.43, 1.1.1.79, 1.1.1.81 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BNJPHLCL_02364 | 1.5e-74 | |||||
BNJPHLCL_02365 | 5e-54 | S | DsrE/DsrF-like family | |||
BNJPHLCL_02366 | 1.5e-209 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
BNJPHLCL_02367 | 1.6e-221 | mvaS | 2.3.3.10 | I | synthase | |
BNJPHLCL_02368 | 1.5e-236 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | I | Hydroxymethylglutaryl-coenzyme A reductase | |
BNJPHLCL_02369 | 3.3e-09 | S | Pfam:DUF1399 | |||
BNJPHLCL_02370 | 3.7e-65 | S | Pfam:DUF1399 | |||
BNJPHLCL_02371 | 5e-213 | G | Major facilitator Superfamily | |||
BNJPHLCL_02372 | 2e-129 | cysL | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
BNJPHLCL_02373 | 3.3e-46 | L | COG2963 Transposase and inactivated derivatives | |||
BNJPHLCL_02374 | 2.9e-38 | L | COG2801 Transposase and inactivated derivatives | |||
BNJPHLCL_02376 | 1.8e-134 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
BNJPHLCL_02377 | 9.2e-37 | T | AMP binding | |||
BNJPHLCL_02378 | 1.4e-33 | L | COG3547 Transposase and inactivated derivatives | |||
BNJPHLCL_02380 | 4.9e-10 | |||||
BNJPHLCL_02381 | 1.4e-117 | kch | P | Ion channel | ||
BNJPHLCL_02382 | 1.5e-180 | ldh1 | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
BNJPHLCL_02383 | 2.5e-75 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
BNJPHLCL_02384 | 1.7e-58 | |||||
BNJPHLCL_02385 | 4.2e-104 | yozB | S | membrane | ||
BNJPHLCL_02386 | 1.1e-77 | ywlE | 3.1.3.48, 3.9.1.2, 5.3.1.6 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
BNJPHLCL_02387 | 4.1e-165 | mcpA | NT | Chemotaxis | ||
BNJPHLCL_02388 | 6.9e-80 | rpiB | 5.3.1.6 | G | Ribose 5-phosphate isomerase | |
BNJPHLCL_02389 | 3.7e-94 | ywlG | S | Belongs to the UPF0340 family | ||
BNJPHLCL_02390 | 1e-131 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BNJPHLCL_02391 | 1.4e-215 | fsr | P | COG0477 Permeases of the major facilitator superfamily | ||
BNJPHLCL_02392 | 2.2e-75 | sleB | 3.5.1.28 | M | Cell wall | |
BNJPHLCL_02393 | 7.8e-148 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
BNJPHLCL_02394 | 3.7e-26 | 1.1.1.31, 1.1.1.60 | I | COG2084 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases | ||
BNJPHLCL_02395 | 7.7e-282 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
BNJPHLCL_02396 | 7.6e-184 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Glucose-1-phosphate adenylyltransferase, GlgD subunit |
BNJPHLCL_02397 | 7.1e-209 | glgC | 2.7.7.27 | G | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
BNJPHLCL_02398 | 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 |
BNJPHLCL_02399 | 6.1e-193 | G | Glycosyl hydrolases family 15 | |||
BNJPHLCL_02400 | 7.3e-21 | S | YpzG-like protein | |||
BNJPHLCL_02401 | 5e-82 | Q | protein disulfide oxidoreductase activity | |||
BNJPHLCL_02402 | 7.1e-89 | ywnH | 2.3.1.183 | M | COG1247 Sortase and related acyltransferases | |
BNJPHLCL_02403 | 5.3e-118 | nudL | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | ||
BNJPHLCL_02404 | 1.1e-223 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BNJPHLCL_02405 | 1.6e-76 | dps | P | Ferritin-like domain | ||
BNJPHLCL_02406 | 5e-81 | V | VanZ like family | |||
BNJPHLCL_02407 | 1.9e-167 | yhcI | S | ABC-2 family transporter protein | ||
BNJPHLCL_02408 | 2e-169 | ydbJ | V | ABC transporter, ATP-binding protein | ||
BNJPHLCL_02409 | 6.3e-57 | |||||
BNJPHLCL_02410 | 6.9e-167 | murB | 1.3.1.98 | M | cell wall formation | |
BNJPHLCL_02411 | 8.1e-80 | S | Protein of unknown function (DUF1189) | |||
BNJPHLCL_02412 | 1.4e-37 | S | Protein of unknown function (DUF1450) | |||
BNJPHLCL_02413 | 6.1e-271 | gnd | 1.1.1.343, 1.1.1.44 | G | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
BNJPHLCL_02414 | 2.3e-48 | I | MaoC like domain | |||
BNJPHLCL_02415 | 4.8e-129 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BNJPHLCL_02416 | 3.6e-53 | dld | 1.1.1.303, 1.1.1.4, 1.1.2.4 | C | Glycolate oxidase subunit | |
BNJPHLCL_02418 | 6.6e-198 | selU | S | tRNA 2-selenouridine synthase | ||
BNJPHLCL_02419 | 1.4e-192 | selD | 2.7.9.3 | E | Synthesizes selenophosphate from selenide and ATP | |
BNJPHLCL_02420 | 4.4e-132 | T | Calcineurin-like phosphoesterase superfamily domain | |||
BNJPHLCL_02422 | 3.1e-187 | yraQ | S | Predicted permease | ||
BNJPHLCL_02423 | 8.1e-227 | proA | 1.2.1.41, 1.2.1.81 | 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 | |
BNJPHLCL_02424 | 2.1e-194 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
BNJPHLCL_02425 | 1.9e-72 | yjlC | S | Protein of unknown function (DUF1641) | ||
BNJPHLCL_02426 | 6.3e-221 | yjlD | 1.6.99.3 | C | NADH dehydrogenase | |
BNJPHLCL_02427 | 1.1e-228 | nrnB | S | phosphohydrolase (DHH superfamily) | ||
BNJPHLCL_02428 | 4.5e-126 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
BNJPHLCL_02429 | 2e-129 | yvpB | NU | protein conserved in bacteria | ||
BNJPHLCL_02430 | 9.2e-50 | tnrA | K | transcriptional | ||
BNJPHLCL_02431 | 7.9e-108 | 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 | |
BNJPHLCL_02432 | 1.9e-23 | S | Virus attachment protein p12 family | |||
BNJPHLCL_02433 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
BNJPHLCL_02434 | 2.4e-36 | feoA | P | COG1918 Fe2 transport system protein A | ||
BNJPHLCL_02435 | 2.1e-174 | L | HKD family nuclease | |||
BNJPHLCL_02436 | 8.4e-53 | nudG | 3.6.1.55, 3.6.1.65 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
BNJPHLCL_02437 | 3.9e-170 | mrr | V | Mrr N-terminal domain | ||
BNJPHLCL_02438 | 0.0 | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | ||
BNJPHLCL_02439 | 3.1e-66 | hsdS-1 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
BNJPHLCL_02440 | 0.0 | hsdM | 2.1.1.72 | V | Type I restriction-modification system | |
BNJPHLCL_02441 | 4e-27 | |||||
BNJPHLCL_02442 | 9.7e-115 | E | LysE type translocator | |||
BNJPHLCL_02443 | 2e-85 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
BNJPHLCL_02444 | 7.6e-80 | 2.7.1.199 | G | COG2190 Phosphotransferase system IIA components | ||
BNJPHLCL_02445 | 2.9e-157 | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases | |
BNJPHLCL_02446 | 1.5e-22 | L | PFAM Transposase, IS4-like | |||
BNJPHLCL_02447 | 3.5e-36 | L | PFAM Transposase, IS4-like | |||
BNJPHLCL_02448 | 1.1e-112 | L | PFAM Transposase, IS4-like | |||
BNJPHLCL_02449 | 3e-118 | S | YqcI/YcgG family | |||
BNJPHLCL_02450 | 1.6e-97 | L | Integrase | |||
BNJPHLCL_02451 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | COG2217 Cation transport ATPase | |
BNJPHLCL_02453 | 6e-280 | yfmM | S | COG0488 ATPase components of ABC transporters with duplicated ATPase domains | ||
BNJPHLCL_02454 | 2.9e-39 | |||||
BNJPHLCL_02455 | 7e-53 | S | SMI1 / KNR4 family (SUKH-1) | |||
BNJPHLCL_02456 | 1.1e-136 | K | helix_turn_helix isocitrate lyase regulation | |||
BNJPHLCL_02457 | 4e-119 | eda | 4.1.2.14, 4.1.3.42 | G | 2-dehydro-3-deoxy-phosphogluconate aldolase | |
BNJPHLCL_02458 | 3.2e-189 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BNJPHLCL_02459 | 5.6e-272 | uxaB | 1.1.1.17, 1.1.1.58 | G | tagaturonate reductase activity | |
BNJPHLCL_02460 | 1.5e-283 | uxaA | 4.2.1.7, 4.4.1.24 | G | Altronate | |
BNJPHLCL_02461 | 9e-283 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
BNJPHLCL_02462 | 4.9e-260 | yjmB | G | MFS/sugar transport protein | ||
BNJPHLCL_02463 | 1.4e-139 | IQ | COG1028 Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BNJPHLCL_02464 | 9.5e-163 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
BNJPHLCL_02465 | 6.4e-179 | kdgK | 2.7.1.45 | G | COG0524 Sugar kinases, ribokinase family | |
BNJPHLCL_02466 | 1.1e-186 | bioB | 2.8.1.6 | H | Catalyzes the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical- based mechanism | |
BNJPHLCL_02467 | 1.7e-244 | NU | cell adhesion | |||
BNJPHLCL_02468 | 0.0 | M | Dolichyl-phosphate-mannose-protein mannosyltransferase | |||
BNJPHLCL_02469 | 3.4e-113 | phnE | 3.6.1.63 | P | ABC transporter | |
BNJPHLCL_02470 | 6.3e-171 | phnD | P | Phosphonate ABC transporter | ||
BNJPHLCL_02471 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
BNJPHLCL_02472 | 2.1e-207 | ysdC | G | COG1363 Cellulase M and related proteins | ||
BNJPHLCL_02473 | 4e-10 | S | double-stranded DNA endodeoxyribonuclease activity | |||
BNJPHLCL_02474 | 3e-12 | S | double-stranded DNA endodeoxyribonuclease activity | |||
BNJPHLCL_02475 | 2.3e-21 | S | Zinc-ribbon containing domain | |||
BNJPHLCL_02476 | 6.3e-299 | yvfH | C | L-lactate permease | ||
BNJPHLCL_02477 | 6.9e-122 | yvfI | K | COG2186 Transcriptional regulators | ||
BNJPHLCL_02478 | 1.8e-228 | lysN | EK | COG1167 Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
BNJPHLCL_02479 | 7e-62 | |||||
BNJPHLCL_02481 | 2.2e-168 | lytR_1 | K | May catalyze the final step in cell wall teichoic acid biosynthesis, the transfer of the anionic cell wall polymers (APs) from their lipid-linked precursor to the cell wall peptidoglycan (PG) | ||
BNJPHLCL_02482 | 5.2e-202 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_02484 | 2.2e-16 | S | YvrJ protein family | |||
BNJPHLCL_02485 | 9.8e-11 | S | Protein of unknown function (DUF2922) | |||
BNJPHLCL_02486 | 2.6e-11 | S | Protein of unknown function (DUF1659) | |||
BNJPHLCL_02487 | 0.0 | O | Belongs to the peptidase S8 family | |||
BNJPHLCL_02488 | 6.6e-69 | S | Protein of unknown function (DUF2512) | |||
BNJPHLCL_02489 | 3.1e-52 | licA | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
BNJPHLCL_02490 | 6.9e-53 | celB | 2.7.1.196, 2.7.1.205, 2.7.1.207 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BNJPHLCL_02491 | 3.7e-12 | |||||
BNJPHLCL_02492 | 1.2e-150 | L | Transposase, IS4 family protein | |||
BNJPHLCL_02493 | 1.8e-153 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
BNJPHLCL_02495 | 2.4e-51 | |||||
BNJPHLCL_02497 | 2.5e-161 | fda | 4.1.2.13 | G | Belongs to the class I fructose-bisphosphate aldolase family | |
BNJPHLCL_02498 | 5e-128 | V | COG1131 ABC-type multidrug transport system, ATPase component | |||
BNJPHLCL_02500 | 5e-205 | ybhR | V | COG0842 ABC-type multidrug transport system, permease component | ||
BNJPHLCL_02501 | 3.5e-112 | K | Transcriptional regulator | |||
BNJPHLCL_02502 | 3.7e-271 | lysP | E | amino acid | ||
BNJPHLCL_02503 | 0.0 | hsdR | 3.1.21.3 | L | COG4096 Type I site-specific restriction-modification system, R (restriction) subunit and related helicases | |
BNJPHLCL_02505 | 1.4e-267 | hsdM | 2.1.1.72 | V | Type I restriction-modification system | |
BNJPHLCL_02506 | 2.1e-255 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
BNJPHLCL_02507 | 7.1e-253 | rocR | KT | COG3829 Transcriptional regulator containing PAS, AAA-type ATPase, and DNA-binding domains | ||
BNJPHLCL_02508 | 1.1e-231 | rocD | 2.6.1.11, 2.6.1.13, 2.6.1.17 | E | Catalyzes the interconversion of ornithine to glutamate semialdehyde | |
BNJPHLCL_02510 | 9.9e-233 | pgaC | GT2 | M | N-acetylglucosaminyltransferase that catalyzes the polymerization of single monomer units of UDP-N-acetylglucosamine to produce the linear homopolymer poly-beta-1,6-N-acetyl-D- glucosamine (PNAG, also referred to as PIA), a biofilm adhesin polysaccharide. Requires IcaD for full activity | |
BNJPHLCL_02511 | 1.1e-47 | icaD | ||||
BNJPHLCL_02512 | 8.4e-148 | icaB | G | Catalyzes the N-deacetylation of poly-beta-1,6-N-acetyl- D-glucosamine (PNAG, also referred to as PIA), a biofilm adhesin polysaccharide | ||
BNJPHLCL_02513 | 9.5e-173 | icaC | G | transferase activity, transferring acyl groups other than amino-acyl groups | ||
BNJPHLCL_02514 | 6.1e-185 | yumC | 1.18.1.2, 1.19.1.1 | C | reductase | |
BNJPHLCL_02515 | 1.4e-228 | yumB | 1.6.99.3 | C | NADH dehydrogenase | |
BNJPHLCL_02516 | 1.2e-46 | yuiB | S | Putative membrane protein | ||
BNJPHLCL_02517 | 1.9e-107 | yuiC | S | protein conserved in bacteria | ||
BNJPHLCL_02518 | 1.4e-298 | pepA | 3.4.11.1, 3.4.11.5 | E | Presumably involved in the processing and regular turnover of intracellular proteins. Catalyzes the removal of unsubstituted N-terminal amino acids from various peptides | |
BNJPHLCL_02520 | 2.6e-297 | gerKA | EG | Spore germination protein | ||
BNJPHLCL_02521 | 9.3e-228 | gerKC | S | spore germination | ||
BNJPHLCL_02522 | 1e-191 | E | Spore germination protein | |||
BNJPHLCL_02524 | 2.8e-55 | yuzC | ||||
BNJPHLCL_02525 | 9.4e-65 | ydiI | Q | protein, possibly involved in aromatic compounds catabolism | ||
BNJPHLCL_02526 | 3e-194 | yuxJ | EGP | Major facilitator Superfamily | ||
BNJPHLCL_02527 | 0.0 | res | 3.1.21.5 | V | Type III restriction enzyme, res subunit | |
BNJPHLCL_02528 | 9.6e-195 | mod | 2.1.1.72 | L | DNA methylase | |
BNJPHLCL_02529 | 1.6e-86 | mntP | P | Probably functions as a manganese efflux pump | ||
BNJPHLCL_02530 | 4.2e-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 | |
BNJPHLCL_02531 | 5.4e-133 | spoIIR | S | Stage II sporulation protein R (spore_II_R) | ||
BNJPHLCL_02532 | 4.1e-161 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
BNJPHLCL_02533 | 8.6e-193 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
BNJPHLCL_02535 | 1.3e-110 | tdk | 2.7.1.21 | F | thymidine kinase | |
BNJPHLCL_02536 | 2.2e-33 | rpmE | J | Ribosomal protein L31 | ||
BNJPHLCL_02537 | 2.7e-230 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
BNJPHLCL_02539 | 2.7e-174 | glpX | 3.1.3.11, 3.1.3.37 | G | fructose-1,6-bisphosphatase | |
BNJPHLCL_02540 | 8.1e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BNJPHLCL_02541 | 2.6e-115 | tal | 2.2.1.2 | G | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
BNJPHLCL_02542 | 3.6e-157 | fbaA | 4.1.2.13, 4.1.2.29 | G | Aldolase | |
BNJPHLCL_02543 | 1.3e-60 | spo0F | T | response regulator | ||
BNJPHLCL_02544 | 0.0 | L | Domain of unknown function (DUF4277) | |||
BNJPHLCL_02545 | 8.9e-239 | LYS1 | 1.5.1.7 | E | Saccharopine dehydrogenase | |
BNJPHLCL_02546 | 4.9e-223 | nspC | 4.1.1.96 | E | Pyridoxal-dependent decarboxylase, C-terminal sheet domain | |
BNJPHLCL_02547 | 8.1e-207 | S | Domain of unknown function (DUF1611_N) Rossmann-like domain | |||
BNJPHLCL_02548 | 4.3e-214 | 5.1.1.12 | E | Alanine racemase, N-terminal domain | ||
BNJPHLCL_02549 | 6.2e-138 | cjaA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
BNJPHLCL_02550 | 1.8e-128 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
BNJPHLCL_02551 | 1.4e-103 | E | amino acid ABC transporter | |||
BNJPHLCL_02552 | 1.2e-75 | papP | E | amino acid ABC transporter | ||
BNJPHLCL_02554 | 5.7e-70 | ydbP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
BNJPHLCL_02555 | 1.3e-213 | rodA | D | Belongs to the SEDS family | ||
BNJPHLCL_02556 | 7.1e-56 | yusN | M | Coat F domain | ||
BNJPHLCL_02557 | 2.4e-40 | |||||
BNJPHLCL_02558 | 2.6e-14 | S | YuzL-like protein | |||
BNJPHLCL_02559 | 0.0 | fadB | 1.1.1.35, 4.2.1.17, 5.1.2.3 | I | 3-hydroxyacyl-CoA dehydrogenase | |
BNJPHLCL_02560 | 3.9e-215 | fadA | 2.3.1.16 | I | Belongs to the thiolase family | |
BNJPHLCL_02561 | 0.0 | fadE | 1.3.8.1 | I | acyl-CoA dehydrogenase | |
BNJPHLCL_02562 | 3.1e-62 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
BNJPHLCL_02563 | 5.1e-63 | gcvH | E | Is also involved in protein lipoylation via its role as an octanoyl lipoyl carrier protein intermediate | ||
BNJPHLCL_02564 | 1.5e-49 | traF | CO | Thioredoxin | ||
BNJPHLCL_02566 | 1.7e-142 | sufC | O | COG0396 ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
BNJPHLCL_02567 | 4.2e-242 | sufD | O | assembly protein SufD | ||
BNJPHLCL_02568 | 1.3e-237 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
BNJPHLCL_02569 | 9.4e-77 | nifU | C | COG0822 NifU homolog involved in Fe-S cluster formation | ||
BNJPHLCL_02570 | 2.2e-273 | sufB | O | FeS cluster assembly | ||
BNJPHLCL_02571 | 2.6e-277 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
BNJPHLCL_02572 | 3.7e-48 | yunC | S | Domain of unknown function (DUF1805) | ||
BNJPHLCL_02573 | 9.4e-127 | yunB | S | Sporulation protein YunB (Spo_YunB) | ||
BNJPHLCL_02574 | 6.7e-200 | lytH | M | Peptidase, M23 | ||
BNJPHLCL_02575 | 1e-173 | lipA | 2.8.1.8 | H | Catalyzes the radical-mediated insertion of two sulfur atoms into the C-6 and C-8 positions of the octanoyl moiety bound to the lipoyl domains of lipoate-dependent enzymes, thereby converting the octanoylated domains into lipoylated derivatives | |
BNJPHLCL_02576 | 2.6e-48 | yutD | S | protein conserved in bacteria | ||
BNJPHLCL_02577 | 4.3e-74 | yutE | S | Protein of unknown function DUF86 | ||
BNJPHLCL_02578 | 3.3e-138 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
BNJPHLCL_02579 | 4.8e-85 | pgpA | 3.1.3.27 | I | COG1267 Phosphatidylglycerophosphatase A and related proteins | |
BNJPHLCL_02580 | 5.8e-199 | yutH | S | Spore coat protein | ||
BNJPHLCL_02581 | 8.6e-37 | nifU | O | COG0694 Thioredoxin-like proteins and domains | ||
BNJPHLCL_02582 | 1.2e-21 | |||||
BNJPHLCL_02583 | 5.7e-197 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
BNJPHLCL_02584 | 9.8e-258 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
BNJPHLCL_02585 | 0.0 | malL | 3.2.1.10 | GH13 | G | COG0366 Glycosidases |
BNJPHLCL_02586 | 0.0 | yvdK | 2.4.1.8 | GH65 | G | Glycoside hydrolase, family 65 |
BNJPHLCL_02587 | 1.9e-147 | malA | S | Protein of unknown function (DUF1189) | ||
BNJPHLCL_02588 | 6.7e-156 | malD | P | transport | ||
BNJPHLCL_02589 | 3.3e-239 | malC | P | COG1175 ABC-type sugar transport systems, permease components | ||
BNJPHLCL_02590 | 4.4e-236 | mdxE | G | COG2182 Maltose-binding periplasmic proteins domains | ||
BNJPHLCL_02591 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Alpha amylase, N-terminal ig-like domain |
BNJPHLCL_02592 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | COG0366 Glycosidases |
BNJPHLCL_02593 | 6.1e-174 | yvdE | K | Transcriptional regulator | ||
BNJPHLCL_02594 | 4.3e-121 | otsB2 | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | Haloacid dehalogenase-like hydrolase |
BNJPHLCL_02595 | 5.5e-107 | E | Lysine exporter protein LysE YggA | |||
BNJPHLCL_02596 | 8.3e-260 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
BNJPHLCL_02597 | 8.1e-132 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BNJPHLCL_02598 | 9.6e-72 | yuiD | S | protein conserved in bacteria | ||
BNJPHLCL_02599 | 2.1e-221 | solA | 1.5.3.1 | E | FAD dependent oxidoreductase | |
BNJPHLCL_02600 | 1.3e-226 | FOXRED | 1.5.3.1 | E | FAD dependent oxidoreductase | |
BNJPHLCL_02601 | 6.5e-276 | ycbD | 1.2.1.3 | C | Catalyzes the oxidation of malonate semialdehyde (MSA) and methylmalonate semialdehyde (MMSA) into acetyl-CoA and propanoyl-CoA, respectively | |
BNJPHLCL_02602 | 5.8e-169 | 4.3.1.12 | E | ornithine cyclodeaminase | ||
BNJPHLCL_02605 | 1.9e-181 | yugO | P | COG1226 Kef-type K transport systems | ||
BNJPHLCL_02606 | 1.3e-259 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
BNJPHLCL_02607 | 3.3e-33 | yuzA | S | Domain of unknown function (DUF378) | ||
BNJPHLCL_02608 | 4e-86 | K | Bacterial transcription activator, effector binding domain | |||
BNJPHLCL_02609 | 1.2e-64 | yugI | 5.3.1.9 | J | RNA binding protein (contains ribosomal protein S1 domain) | |
BNJPHLCL_02610 | 5.9e-29 | K | Helix-turn-helix XRE-family like proteins | |||
BNJPHLCL_02611 | 1.6e-196 | namA | C | Catalyzes the reduction of the double bond of an array of alpha,beta-unsaturated aldehydes and ketones. It also reduces the nitro group of nitroester and nitroaromatic compounds. It could have a role in detoxification processes | ||
BNJPHLCL_02612 | 1e-164 | S | reductase | |||
BNJPHLCL_02613 | 2.4e-158 | dkgB | S | Aldo/keto reductase family | ||
BNJPHLCL_02614 | 3e-237 | S | protein conserved in bacteria | |||
BNJPHLCL_02616 | 2.7e-111 | ppiB | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
BNJPHLCL_02617 | 1.4e-85 | L | Mu transposase, C-terminal | |||
BNJPHLCL_02618 | 1.1e-13 | |||||
BNJPHLCL_02619 | 6.3e-49 | S | Family of unknown function (DUF5316) | |||
BNJPHLCL_02620 | 1.6e-123 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNJPHLCL_02621 | 0.0 | phoR | 2.7.13.3 | T | Signal transduction histidine kinase | |
BNJPHLCL_02623 | 2e-258 | hemY2 | 1.3.3.15, 1.3.3.4 | H | Catalyzes the 6-electron oxidation of protoporphyrinogen-IX to form protoporphyrin-IX | |
BNJPHLCL_02624 | 5.5e-161 | pstS | P | Phosphate | ||
BNJPHLCL_02625 | 1.4e-157 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
BNJPHLCL_02626 | 4.8e-157 | pstA | P | Phosphate transport system permease | ||
BNJPHLCL_02627 | 2.1e-146 | 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 | |
BNJPHLCL_02628 | 6e-143 | 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 | |
BNJPHLCL_02629 | 2.5e-30 | S | EamA-like transporter family | |||
BNJPHLCL_02630 | 1.4e-118 | yfbR | S | HD containing hydrolase-like enzyme | ||
BNJPHLCL_02631 | 2.4e-34 | csbA | S | protein conserved in bacteria | ||
BNJPHLCL_02632 | 1.6e-09 | S | Uncharacterized conserved protein (DUF2164) | |||
BNJPHLCL_02633 | 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 | ||
BNJPHLCL_02634 | 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 | ||
BNJPHLCL_02637 | 9.1e-33 | S | Protein of unknown function (DUF2933) | |||
BNJPHLCL_02639 | 3.2e-248 | T | PhoQ Sensor | |||
BNJPHLCL_02640 | 1.5e-126 | KT | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNJPHLCL_02641 | 4.9e-91 | ydhK | M | Protein of unknown function (DUF1541) | ||
BNJPHLCL_02642 | 5.2e-93 | VY92_08700 | S | Enoyl-(Acyl carrier protein) reductase | ||
BNJPHLCL_02643 | 4.1e-12 | recN | L | Putative cell-wall binding lipoprotein | ||
BNJPHLCL_02644 | 2.7e-174 | nodB1 | G | deacetylase | ||
BNJPHLCL_02646 | 1.3e-25 | L | Archaeal putative transposase ISC1217 | |||
BNJPHLCL_02647 | 2.5e-15 | S | Ribbon-helix-helix protein, copG family | |||
BNJPHLCL_02648 | 9.3e-223 | gltT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
BNJPHLCL_02649 | 0.0 | 2.7.1.201, 2.7.1.211 | G | phosphotransferase system | ||
BNJPHLCL_02650 | 4.8e-154 | glcT | K | antiterminator | ||
BNJPHLCL_02651 | 4.3e-234 | pbuG | S | permease | ||
BNJPHLCL_02653 | 0.0 | ywjA | V | ABC transporter | ||
BNJPHLCL_02654 | 8e-211 | ynfM | EGP | Major facilitator Superfamily | ||
BNJPHLCL_02656 | 3.4e-13 | S | PFAM Uncharacterised protein family UPF0236 | |||
BNJPHLCL_02658 | 2.7e-253 | ybhI | P | Sodium:sulfate symporter transmembrane region | ||
BNJPHLCL_02659 | 3.2e-50 | L | deoxyribonuclease I activity | |||
BNJPHLCL_02660 | 0.0 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
BNJPHLCL_02664 | 1.1e-237 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | ||
BNJPHLCL_02665 | 7.8e-227 | 2.3.1.179 | IQ | Beta-ketoacyl synthase, C-terminal domain | ||
BNJPHLCL_02666 | 7.5e-37 | bofA | S | Sigma-K factor-processing regulatory protein BofA | ||
BNJPHLCL_02667 | 3.4e-08 | yaaL | S | Protein of unknown function (DUF2508) | ||
BNJPHLCL_02668 | 1.5e-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 | ||
BNJPHLCL_02669 | 1.3e-35 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
BNJPHLCL_02670 | 5.3e-306 | 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 | |
BNJPHLCL_02671 | 2.1e-88 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
BNJPHLCL_02673 | 1.1e-142 | yaaH | M | Glycoside Hydrolase Family | ||
BNJPHLCL_02674 | 1.4e-118 | dgk | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxyguanosine kinase | |
BNJPHLCL_02675 | 3.3e-126 | dck | 2.7.1.113, 2.7.1.74, 2.7.1.76 | F | Deoxycytidine kinase | |
BNJPHLCL_02676 | 2.9e-09 | |||||
BNJPHLCL_02677 | 2.9e-211 | 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) | |
BNJPHLCL_02678 | 1.3e-102 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
BNJPHLCL_02679 | 3.7e-157 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
BNJPHLCL_02680 | 2.7e-241 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNJPHLCL_02681 | 1.5e-272 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
BNJPHLCL_02682 | 8.1e-179 | yaaC | S | YaaC-like Protein | ||
BNJPHLCL_02683 | 4.4e-29 | K | Helix-turn-helix XRE-family like proteins | |||
BNJPHLCL_02685 | 9.2e-233 | wbbX | GT2,GT4 | M | transferase activity, transferring glycosyl groups | |
BNJPHLCL_02686 | 2.2e-26 | |||||
BNJPHLCL_02687 | 3.4e-150 | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | |||
BNJPHLCL_02688 | 9.3e-116 | sapB | S | MgtC SapB transporter | ||
BNJPHLCL_02689 | 1.2e-165 | S | Protein of unknown function (DUF1646) | |||
BNJPHLCL_02690 | 7.3e-30 | EGP | Major facilitator Superfamily | |||
BNJPHLCL_02691 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
BNJPHLCL_02692 | 4e-30 | P | Copper resistance protein CopZ | |||
BNJPHLCL_02693 | 8.4e-57 | S | protein conserved in bacteria | |||
BNJPHLCL_02694 | 2.5e-68 | lrpC | K | Transcriptional regulator | ||
BNJPHLCL_02695 | 8.6e-72 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | |||
BNJPHLCL_02696 | 5.5e-225 | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | ||
BNJPHLCL_02697 | 1.3e-27 | yhjC | S | Protein of unknown function (DUF3311) | ||
BNJPHLCL_02698 | 1.2e-266 | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | |||
BNJPHLCL_02700 | 1.5e-30 | S | Domain of unknown function (DUF202) | |||
BNJPHLCL_02701 | 1.9e-102 | P | Integral membrane protein TerC family | |||
BNJPHLCL_02702 | 1.3e-11 | L | Transposase, IS4 family protein | |||
BNJPHLCL_02703 | 1.5e-93 | cwlS | 3.5.1.28 | CBM50 | M | COG1388 FOG LysM repeat |
BNJPHLCL_02704 | 2.5e-80 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BNJPHLCL_02705 | 0.0 | yfiB | V | ABC transporter | ||
BNJPHLCL_02706 | 0.0 | yfiC | V | COG1132 ABC-type multidrug transport system, ATPase and permease components | ||
BNJPHLCL_02707 | 3.4e-233 | ybbC | 3.2.1.52 | S | protein conserved in bacteria | |
BNJPHLCL_02708 | 4.3e-308 | ampC | V | Belongs to the UPF0214 family | ||
BNJPHLCL_02709 | 0.0 | nagA | 3.2.1.52 | G | Belongs to the glycosyl hydrolase 3 family | |
BNJPHLCL_02710 | 2.5e-10 | yokF | 3.1.31.1 | L | RNA catabolic process | |
BNJPHLCL_02712 | 4.5e-16 | S | IrrE N-terminal-like domain | |||
BNJPHLCL_02713 | 1.8e-18 | K | Helix-turn-helix XRE-family like proteins | |||
BNJPHLCL_02714 | 1.3e-16 | 2.3.1.19 | K | sequence-specific DNA binding | ||
BNJPHLCL_02715 | 7.8e-58 | K | BRO family, N-terminal domain | |||
BNJPHLCL_02716 | 7.3e-15 | S | Helix-turn-helix domain | |||
BNJPHLCL_02717 | 1.4e-15 | |||||
BNJPHLCL_02722 | 3.6e-10 | S | Hypothetical protein Yqai | |||
BNJPHLCL_02723 | 7.7e-137 | yqaJ | L | YqaJ-like viral recombinase domain | ||
BNJPHLCL_02724 | 8e-123 | recT | L | RecT family | ||
BNJPHLCL_02725 | 9.6e-27 | L | Replication initiation and membrane attachment | |||
BNJPHLCL_02726 | 1.3e-13 | xkdC | L | Bacterial dnaA protein | ||
BNJPHLCL_02727 | 5e-90 | xkdC | L | Bacterial dnaA protein | ||
BNJPHLCL_02731 | 4.6e-45 | S | dUTPase | |||
BNJPHLCL_02732 | 1.5e-53 | S | Protein of unknown function (DUF1064) | |||
BNJPHLCL_02733 | 1.7e-48 | V | N-6 DNA Methylase | |||
BNJPHLCL_02734 | 2.5e-13 | S | Protein of unknown function (DUF3954) | |||
BNJPHLCL_02739 | 1.3e-07 | |||||
BNJPHLCL_02740 | 3.5e-103 | ydcA | 3.4.21.105 | S | membrane protein (homolog of Drosophila rhomboid) | |
BNJPHLCL_02741 | 4.2e-56 | 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 | |
BNJPHLCL_02742 | 1.1e-189 | ydcC | M | COG2834 Outer membrane lipoprotein-sorting protein | ||
BNJPHLCL_02743 | 1.7e-215 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
BNJPHLCL_02744 | 2e-40 | ndoAI | K | transcriptional regulators containing the CopG Arc MetJ DNA-binding domain and a metal-binding domain | ||
BNJPHLCL_02745 | 7.2e-56 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
BNJPHLCL_02746 | 4.8e-151 | rsbR | T | Positive regulator of sigma-B | ||
BNJPHLCL_02747 | 8.1e-55 | rsbS | T | antagonist | ||
BNJPHLCL_02748 | 2.9e-69 | rsbT | 2.7.11.1 | T | COG2172 Anti-sigma regulatory factor (Ser Thr protein kinase) | |
BNJPHLCL_02749 | 2.5e-186 | rsbU | 3.1.3.3 | KT | phosphatase | |
BNJPHLCL_02750 | 4e-54 | rsbV | T | Belongs to the anti-sigma-factor antagonist family | ||
BNJPHLCL_02751 | 6.7e-81 | rsbW | 2.7.11.1 | T | Negative regulator of sigma-B activity. Phosphorylates and inactivates its specific antagonist protein, RsbV. Upon phosphorylation of RsbV, RsbW is released and binds to sigma-B, thereby blocking its ability to form an RNA polymerase holoenzyme (E-sigma-B) | |
BNJPHLCL_02752 | 9.2e-136 | sigB | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released | ||
BNJPHLCL_02753 | 5.2e-107 | rsbX | 3.1.3.16, 3.1.3.3 | KT | Sigma factor PP2C-like phosphatases | |
BNJPHLCL_02754 | 0.0 | yhgF | K | COG2183 Transcriptional accessory protein | ||
BNJPHLCL_02755 | 3e-92 | ydcK | S | Belongs to the SprT family | ||
BNJPHLCL_02763 | 1.6e-08 | |||||
BNJPHLCL_02768 | 2.1e-12 | yodH | Q | Methyltransferase | ||
BNJPHLCL_02769 | 7.3e-66 | yodH | Q | Methyltransferase | ||
BNJPHLCL_02770 | 0.0 | gtfC | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein |
BNJPHLCL_02771 | 2.1e-162 | S | HipA-like C-terminal domain | |||
BNJPHLCL_02772 | 1.6e-145 | S | HIRAN domain | |||
BNJPHLCL_02773 | 6e-67 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
BNJPHLCL_02774 | 3.2e-178 | 1.13.12.16, 1.3.1.9 | S | COG2070 Dioxygenases related to 2-nitropropane dioxygenase | ||
BNJPHLCL_02775 | 5.4e-67 | yjbR | S | YjbR | ||
BNJPHLCL_02776 | 1.9e-65 | S | Protein of unknown function (DUF1648) | |||
BNJPHLCL_02777 | 2.3e-240 | L | Metallo-beta-lactamase superfamily | |||
BNJPHLCL_02778 | 2.8e-26 | S | Protein of unknown function (DUF3006) | |||
BNJPHLCL_02779 | 0.0 | L | Metal dependent phosphohydrolases with conserved 'HD' motif. | |||
BNJPHLCL_02780 | 2.1e-42 | S | CRISPR-associated protein | |||
BNJPHLCL_02782 | 7.4e-26 | S | Protein of unknown function (DUF1617) | |||
BNJPHLCL_02783 | 5.2e-33 | D | nuclear chromosome segregation | |||
BNJPHLCL_02784 | 1.4e-168 | |||||
BNJPHLCL_02785 | 1.2e-30 | S | HNH endonuclease | |||
BNJPHLCL_02786 | 7.3e-271 | S | Phage tail protein | |||
BNJPHLCL_02787 | 1.1e-128 | L | Transglycosylase SLT domain | |||
BNJPHLCL_02788 | 8.5e-52 | S | Bacteriophage Gp15 protein | |||
BNJPHLCL_02790 | 6.9e-100 | radC | E | Belongs to the UPF0758 family | ||
BNJPHLCL_02791 | 1.1e-165 | spoIIB | ||||
BNJPHLCL_02792 | 3.8e-142 | comC | 3.4.23.43 | NOU | COG1989 Type II secretory pathway, prepilin signal peptidase PulO and related peptidases | |
BNJPHLCL_02793 | 1.2e-97 | |||||
BNJPHLCL_02794 | 2.3e-81 | pilN | NU | PFAM Fimbrial assembly family protein | ||
BNJPHLCL_02795 | 6e-180 | NU | COG4972 Tfp pilus assembly protein, ATPase PilM | |||
BNJPHLCL_02796 | 1.2e-16 | NU | cell adhesion | |||
BNJPHLCL_02797 | 1.9e-201 | pilC | NU | type II secretion system | ||
BNJPHLCL_02798 | 1.3e-193 | pilT | NU | twitching motility protein | ||
BNJPHLCL_02799 | 5.8e-289 | pilB | NU | COG2804 Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
BNJPHLCL_02800 | 1.1e-195 | V | G5 | |||
BNJPHLCL_02801 | 5.1e-120 | S | PRC-barrel domain | |||
BNJPHLCL_02802 | 2.9e-145 | |||||
BNJPHLCL_02803 | 1.3e-90 | yfkM | 3.5.1.124 | S | protease | |
BNJPHLCL_02804 | 1.2e-143 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
BNJPHLCL_02805 | 7.3e-33 | yfkK | S | Belongs to the UPF0435 family | ||
BNJPHLCL_02806 | 3.1e-145 | yihY | S | Belongs to the UPF0761 family | ||
BNJPHLCL_02807 | 7e-220 | yfkF | EGP | Major facilitator Superfamily | ||
BNJPHLCL_02808 | 2.9e-172 | cax | P | COG0387 Ca2 H antiporter | ||
BNJPHLCL_02809 | 9e-147 | yfkD | S | YfkD-like protein | ||
BNJPHLCL_02810 | 1.5e-26 | yfjT | ||||
BNJPHLCL_02811 | 7.3e-149 | pdaA | G | deacetylase | ||
BNJPHLCL_02812 | 3.2e-166 | yfjP | 3.2.2.21 | L | COG0122 3-methyladenine DNA glycosylase 8-oxoguanine DNA glycosylase | |
BNJPHLCL_02813 | 3.3e-253 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BNJPHLCL_02814 | 8.2e-100 | K | DNA-binding transcription factor activity | |||
BNJPHLCL_02815 | 4.7e-190 | lmrA | 3.6.3.44 | V | ABC transporter | |
BNJPHLCL_02816 | 5e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
BNJPHLCL_02817 | 6.8e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
BNJPHLCL_02818 | 6.8e-116 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
BNJPHLCL_02819 | 5.7e-166 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
BNJPHLCL_02820 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
BNJPHLCL_02821 | 1.5e-135 | stp | 3.1.3.16 | T | phosphatase | |
BNJPHLCL_02822 | 5.8e-255 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
BNJPHLCL_02823 | 1.7e-179 | 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 | |
BNJPHLCL_02824 | 1.9e-83 | def | 2.1.2.9, 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 | |
BNJPHLCL_02825 | 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 | ||
BNJPHLCL_02826 | 1.1e-220 | 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 | |
BNJPHLCL_02827 | 3.4e-29 | 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 | |
BNJPHLCL_02828 | 3.7e-108 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
BNJPHLCL_02829 | 1.1e-44 | ylzA | S | Belongs to the UPF0296 family | ||
BNJPHLCL_02830 | 1.3e-151 | yicC | S | stress-induced protein | ||
BNJPHLCL_02831 | 0.0 | yloB | 3.6.3.8 | P | COG0474 Cation transport ATPase | |
BNJPHLCL_02832 | 0.0 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
BNJPHLCL_02833 | 9.6e-167 | yocS | S | -transporter | ||
BNJPHLCL_02834 | 1.9e-106 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
BNJPHLCL_02835 | 1.2e-124 | M | Non-essential cell division protein that could be required for efficient cell constriction | |||
BNJPHLCL_02836 | 3.2e-59 | croE | S | Helix-turn-helix | ||
BNJPHLCL_02837 | 3.5e-135 | E | IrrE N-terminal-like domain | |||
BNJPHLCL_02838 | 1.1e-38 | |||||
BNJPHLCL_02839 | 4.1e-78 | yicJ | G | MFS/sugar transport protein | ||
BNJPHLCL_02840 | 2.2e-154 | yicJ | G | MFS/sugar transport protein | ||
BNJPHLCL_02841 | 1.5e-299 | 2.7.1.12, 2.7.1.17 | G | xylulose kinase | ||
BNJPHLCL_02843 | 3.6e-221 | adhB | 1.1.1.1, 1.1.1.14, 1.1.1.284 | E | COG1063 Threonine dehydrogenase and related Zn-dependent dehydrogenases | |
BNJPHLCL_02844 | 1.6e-111 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
BNJPHLCL_02845 | 5.2e-178 | 3.1.1.5 | I | Alpha beta hydrolase | ||
BNJPHLCL_02847 | 2.4e-234 | atl | 3.2.1.96, 3.5.1.28 | GH73 | G | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase |
BNJPHLCL_02848 | 3.4e-163 | ygxA | S | Nucleotidyltransferase-like | ||
BNJPHLCL_02849 | 5e-57 | ygzB | S | UPF0295 protein | ||
BNJPHLCL_02850 | 2.9e-139 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
BNJPHLCL_02851 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BNJPHLCL_02852 | 1.5e-163 | alsR | K | Transcriptional regulator | ||
BNJPHLCL_02853 | 5.4e-87 | iprA | K | Transcriptional regulator | ||
BNJPHLCL_02855 | 2.9e-81 | perR | P | Belongs to the Fur family | ||
BNJPHLCL_02856 | 2.3e-101 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | Adenosyltransferase | |
BNJPHLCL_02858 | 3.4e-65 | P | Ion transport | |||
BNJPHLCL_02859 | 1.1e-247 | gsaB | 5.4.3.8 | H | Glutamate-1-semialdehyde aminotransferase | |
BNJPHLCL_02860 | 5.5e-16 | |||||
BNJPHLCL_02861 | 6.1e-39 | S | Minor capsid protein from bacteriophage | |||
BNJPHLCL_02862 | 6.2e-31 | S | Minor capsid protein | |||
BNJPHLCL_02863 | 3.6e-07 | S | Minor capsid protein | |||
BNJPHLCL_02864 | 1.5e-14 | |||||
BNJPHLCL_02865 | 6.7e-13 | |||||
BNJPHLCL_02866 | 1e-125 | |||||
BNJPHLCL_02867 | 5.9e-22 | |||||
BNJPHLCL_02868 | 3.7e-12 | |||||
BNJPHLCL_02871 | 4.8e-130 | M | Phage minor capsid protein 2 | |||
BNJPHLCL_02872 | 8.6e-154 | S | portal protein | |||
BNJPHLCL_02873 | 4.6e-201 | S | Terminase RNAseH like domain | |||
BNJPHLCL_02874 | 7.5e-82 | yqaS | L | DNA packaging | ||
BNJPHLCL_02876 | 1.2e-37 | L | Transposase | |||
BNJPHLCL_02877 | 4.8e-229 | patB | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
BNJPHLCL_02878 | 6.7e-108 | 4.1.1.44 | S | Antioxidant protein with alkyl hydroperoxidase activity. Required for the reduction of the AhpC active site cysteine residues and for the regeneration of the AhpC enzyme activity | ||
BNJPHLCL_02879 | 5.8e-197 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
BNJPHLCL_02880 | 1.9e-111 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
BNJPHLCL_02881 | 5.2e-206 | U | protein localization to endoplasmic reticulum | |||
BNJPHLCL_02882 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
BNJPHLCL_02883 | 9.4e-91 | nrdG | 1.97.1.4 | O | 4Fe-4S single cluster domain | |
BNJPHLCL_02885 | 5.7e-220 | gltP | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
BNJPHLCL_02886 | 1.3e-165 | mleR | K | LysR substrate binding domain | ||
BNJPHLCL_02887 | 4.9e-76 | |||||
BNJPHLCL_02889 | 5.5e-138 | pdaB | 3.5.1.104 | G | xylanase chitin deacetylase | |
BNJPHLCL_02890 | 1.2e-30 | |||||
BNJPHLCL_02891 | 1.6e-260 | cydA | 1.10.3.14 | C | oxidase, subunit | |
BNJPHLCL_02892 | 2.2e-182 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase, subunit II | |
BNJPHLCL_02893 | 0.0 | cydD | V | ATP-binding | ||
BNJPHLCL_02894 | 0.0 | cydD | V | ATP-binding protein | ||
BNJPHLCL_02895 | 5.7e-48 | L | IstB-like ATP binding protein | |||
BNJPHLCL_02896 | 1.1e-59 | arsR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BNJPHLCL_02897 | 2.4e-179 | arsB | 1.20.4.1 | P | Sodium Bile acid symporter family | |
BNJPHLCL_02898 | 4.2e-66 | arsC | 1.20.4.1 | T | Catalyzes the reduction of arsenate As(V) to arsenite As(III) | |
BNJPHLCL_02899 | 6.1e-58 | S | Arsenical resistance operon trans-acting repressor ArsD | |||
BNJPHLCL_02900 | 2.1e-223 | arsA | 3.6.3.16 | D | 4Fe-4S iron sulfur cluster binding proteins, NifH/frxC family | |
BNJPHLCL_02901 | 7.5e-197 | M1-161 | T | HD domain | ||
BNJPHLCL_02902 | 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 | |
BNJPHLCL_02903 | 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 | |
BNJPHLCL_02904 | 9.6e-11 | yaaB | S | Domain of unknown function (DUF370) | ||
BNJPHLCL_02905 | 3.5e-205 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
BNJPHLCL_02906 | 2.7e-32 | yaaA | S | S4 domain | ||
BNJPHLCL_02909 | 5.6e-75 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
BNJPHLCL_02910 | 1.4e-210 | htrA | 3.4.21.107 | O | COG0265 Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain | |
BNJPHLCL_02911 | 9e-147 | vicX | 3.1.26.11 | S | COG1235 Metal-dependent hydrolases of the beta-lactamase superfamily I | |
BNJPHLCL_02912 | 4.3e-141 | yycI | S | protein conserved in bacteria | ||
BNJPHLCL_02913 | 2.9e-243 | yycH | S | protein conserved in bacteria | ||
BNJPHLCL_02914 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
BNJPHLCL_02915 | 1.7e-133 | T | COG0745 Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNJPHLCL_02916 | 5.7e-130 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
BNJPHLCL_02917 | 4.6e-123 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
BNJPHLCL_02918 | 1.1e-09 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
BNJPHLCL_02919 | 0.0 | ydiF | S | ABC transporter | ||
BNJPHLCL_02920 | 8.1e-185 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
BNJPHLCL_02921 | 2.2e-81 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
BNJPHLCL_02922 | 2.8e-128 | yeaZ | 2.3.1.234 | O | COG1214 Inactive homolog of metal-dependent proteases | |
BNJPHLCL_02923 | 5.3e-83 | ydiB | 2.7.1.221, 5.1.1.1 | S | ATPase or kinase | |
BNJPHLCL_02925 | 1.3e-60 | S | Domain of unknown function (DUF2935) | |||
BNJPHLCL_02926 | 4.5e-146 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
BNJPHLCL_02927 | 4e-248 | ugpB | G | Glycerol-3-phosphate ABC transporter substrate-binding protein | ||
BNJPHLCL_02929 | 1.9e-147 | ugpE | P | Glycerol-3-phosphate ABC transporter permease | ||
BNJPHLCL_02930 | 2.2e-168 | ugpA | G | ABC transporter (permease) | ||
BNJPHLCL_02931 | 1.4e-206 | ugpC | 3.6.3.20 | P | Belongs to the ABC transporter superfamily | |
BNJPHLCL_02932 | 1.2e-29 | 3.2.1.78 | GH26 | O | cellulase activity | |
BNJPHLCL_02933 | 9.3e-35 | cps4F | 2.4.1.306 | GT4 | M | Glycosyltransferase Family 4 |
BNJPHLCL_02934 | 1.6e-20 | I | CDP-alcohol phosphatidyltransferase | |||
BNJPHLCL_02935 | 1.5e-35 | GT2 | M | transferase activity, transferring glycosyl groups | ||
BNJPHLCL_02936 | 1.1e-54 | M | Glycosyltransferase like family 2 | |||
BNJPHLCL_02937 | 4.3e-147 | cps1C | S | COG2244 Membrane protein involved in the export of O-antigen and teichoic acid | ||
BNJPHLCL_02938 | 5e-63 | |||||
BNJPHLCL_02939 | 1.8e-34 | L | Transposase, IS4 family protein | |||
BNJPHLCL_02940 | 2.2e-19 | |||||
BNJPHLCL_02942 | 3.6e-82 | ybbK | 2.4.2.1, 6.3.2.4 | S | Protein of unknown function (DUF523) | |
BNJPHLCL_02943 | 7.2e-98 | O | HI0933-like protein | |||
BNJPHLCL_02944 | 1.6e-79 | K | Acetyltransferase (GNAT) domain | |||
BNJPHLCL_02945 | 9.7e-19 | |||||
BNJPHLCL_02946 | 6.3e-09 | S | transposase or invertase | |||
BNJPHLCL_02947 | 5e-81 | smpB | O | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene | ||
BNJPHLCL_02948 | 0.0 | rnr | K | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
BNJPHLCL_02949 | 3.4e-143 | est | 3.1.1.1 | S | Carboxylesterase | |
BNJPHLCL_02950 | 4.2e-28 | secG | U | Preprotein translocase subunit SecG | ||
BNJPHLCL_02951 | 1.3e-240 | 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 | |
BNJPHLCL_02953 | 2.3e-300 | gpmI | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and | |
BNJPHLCL_02954 | 1.1e-122 | 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) | |
BNJPHLCL_02955 | 5.9e-219 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
BNJPHLCL_02956 | 9.9e-183 | gapA | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BNJPHLCL_02957 | 2.2e-185 | cggR | K | COG2390 Transcriptional regulator, contains sigma factor-related N-terminal domain | ||
BNJPHLCL_02958 | 2.3e-39 | XAC3035 | O | Has a glutathione-disulfide oxidoreductase activity in the presence of NADPH and glutathione reductase. Reduces low molecular weight disulfides and proteins | ||
BNJPHLCL_02959 | 1.2e-244 | rpoN | K | COG1508 DNA-directed RNA polymerase specialized sigma subunit, sigma54 homolog | ||
BNJPHLCL_02960 | 1.2e-244 | E | COG1113 Gamma-aminobutyrate permease and related permeases | |||
BNJPHLCL_02961 | 1.2e-97 | ydjA | C | Nitroreductase family | ||
BNJPHLCL_02962 | 5.4e-175 | iolS | C | Aldo keto reductase | ||
BNJPHLCL_02963 | 1.2e-83 | cotF | M | Spore coat protein | ||
BNJPHLCL_02964 | 2.6e-92 | hxlB | 4.1.2.14, 4.1.2.43, 4.1.3.42, 5.3.1.27 | M | SIS domain | |
BNJPHLCL_02965 | 2.6e-35 | ptxS | K | transcriptional | ||
BNJPHLCL_02967 | 1.8e-206 | yleB | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | |
BNJPHLCL_02968 | 1.7e-149 | 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 | |
BNJPHLCL_02969 | 6.2e-250 | sacX | 2.7.1.201, 2.7.1.211 | G | phosphotransferase system | |
BNJPHLCL_02970 | 2.6e-147 | K | transcriptional | |||
BNJPHLCL_02971 | 3.2e-187 | ygaE | S | Membrane | ||
BNJPHLCL_02972 | 7e-38 | yqhV | S | Protein of unknown function (DUF2619) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)