ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
BNMOMFGJ_00001 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
BNMOMFGJ_00002 | 1e-44 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
BNMOMFGJ_00003 | 1.2e-87 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
BNMOMFGJ_00004 | 1.3e-111 | 2.7.13.3 | T | protein histidine kinase activity | ||
BNMOMFGJ_00005 | 2.4e-101 | yjbK | S | Adenylate cyclase | ||
BNMOMFGJ_00006 | 8.4e-131 | ecsA | V | abc transporter atp-binding protein | ||
BNMOMFGJ_00007 | 3.5e-87 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
BNMOMFGJ_00008 | 6.8e-93 | parB | K | Belongs to the ParB family | ||
BNMOMFGJ_00009 | 8.8e-68 | tdk | 2.7.1.21 | F | thymidine kinase | |
BNMOMFGJ_00010 | 2e-33 | secG | U | Preprotein translocase subunit SecG | ||
BNMOMFGJ_00011 | 7.8e-58 | mdtG | EGP | Major facilitator Superfamily | ||
BNMOMFGJ_00012 | 8.7e-20 | 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 | ||
BNMOMFGJ_00013 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
BNMOMFGJ_00014 | 9.5e-144 | ylmH | S | conserved protein, contains S4-like domain | ||
BNMOMFGJ_00015 | 8.4e-138 | divIVA | D | Cell division initiation protein | ||
BNMOMFGJ_00016 | 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) | |
BNMOMFGJ_00017 | 3.8e-184 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BNMOMFGJ_00018 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BNMOMFGJ_00019 | 2.2e-34 | nrdH | O | Glutaredoxin | ||
BNMOMFGJ_00020 | 1.5e-12 | |||||
BNMOMFGJ_00021 | 4e-122 | 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 | |
BNMOMFGJ_00022 | 1.4e-119 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
BNMOMFGJ_00023 | 3e-162 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
BNMOMFGJ_00024 | 0.0 | M | family 8 | |||
BNMOMFGJ_00025 | 1.6e-211 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
BNMOMFGJ_00026 | 1.6e-288 | asp1 | S | Accessory Sec system protein Asp1 | ||
BNMOMFGJ_00027 | 3.2e-289 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
BNMOMFGJ_00028 | 3.8e-78 | asp3 | S | Accessory Sec system protein Asp3 | ||
BNMOMFGJ_00029 | 7.5e-38 | mmuP | E | amino acid | ||
BNMOMFGJ_00030 | 1.9e-135 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
BNMOMFGJ_00031 | 1.8e-23 | U | protein secretion | |||
BNMOMFGJ_00032 | 8.4e-185 | lmrA1 | V | abc transporter atp-binding protein | ||
BNMOMFGJ_00033 | 5.8e-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 | ||
BNMOMFGJ_00034 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
BNMOMFGJ_00035 | 1e-246 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BNMOMFGJ_00036 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
BNMOMFGJ_00037 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
BNMOMFGJ_00038 | 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 | ||
BNMOMFGJ_00039 | 2.4e-99 | yvbG | U | UPF0056 membrane protein | ||
BNMOMFGJ_00040 | 1.3e-113 | 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 | |
BNMOMFGJ_00042 | 2.2e-95 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
BNMOMFGJ_00043 | 6.6e-159 | thrC | 4.2.3.1 | E | Threonine synthase | |
BNMOMFGJ_00044 | 1.5e-89 | |||||
BNMOMFGJ_00045 | 3.5e-128 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
BNMOMFGJ_00046 | 3.5e-52 | XK27_02985 | S | overlaps another CDS with the same product name | ||
BNMOMFGJ_00047 | 3.6e-28 | XK27_05745 | ||||
BNMOMFGJ_00048 | 6.4e-38 | yxeN | P | ABC transporter (Permease | ||
BNMOMFGJ_00049 | 4.2e-130 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
BNMOMFGJ_00050 | 5.1e-41 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
BNMOMFGJ_00051 | 6e-79 | S | Protein of unknown function (DUF3021) | |||
BNMOMFGJ_00052 | 3.8e-133 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
BNMOMFGJ_00053 | 2.9e-170 | 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 | |
BNMOMFGJ_00054 | 1.9e-95 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
BNMOMFGJ_00055 | 1e-151 | yfmR | S | abc transporter atp-binding protein | ||
BNMOMFGJ_00056 | 1.2e-55 | K | Transcriptional regulator | |||
BNMOMFGJ_00057 | 2.4e-74 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
BNMOMFGJ_00058 | 4.3e-62 | clpE | O | Belongs to the ClpA ClpB family | ||
BNMOMFGJ_00059 | 7.7e-24 | S | KAP family P-loop domain | |||
BNMOMFGJ_00060 | 2.8e-30 | CP_0600 | 3.5.4.2, 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
BNMOMFGJ_00061 | 2.4e-29 | S | KAP family P-loop domain | |||
BNMOMFGJ_00062 | 2.2e-66 | 1.14.13.22 | S | Uncharacterised nucleotidyltransferase | ||
BNMOMFGJ_00063 | 4.2e-133 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
BNMOMFGJ_00064 | 8.3e-87 | ykuL | S | CBS domain | ||
BNMOMFGJ_00065 | 5.1e-98 | XK27_09740 | S | Phosphoesterase | ||
BNMOMFGJ_00066 | 5.6e-183 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
BNMOMFGJ_00067 | 3.4e-149 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BNMOMFGJ_00068 | 1.6e-36 | yneF | S | UPF0154 protein | ||
BNMOMFGJ_00069 | 5.3e-90 | K | transcriptional regulator | |||
BNMOMFGJ_00070 | 3.6e-243 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
BNMOMFGJ_00071 | 1.9e-12 | ycdA | S | Domain of unknown function (DUF4352) | ||
BNMOMFGJ_00072 | 2.5e-170 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
BNMOMFGJ_00073 | 1.2e-25 | WQ51_00785 | ||||
BNMOMFGJ_00074 | 4.6e-50 | S | TM2 domain | |||
BNMOMFGJ_00075 | 7.4e-247 | 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 | |
BNMOMFGJ_00076 | 3.1e-75 | yueI | S | Protein of unknown function (DUF1694) | ||
BNMOMFGJ_00077 | 9.3e-198 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
BNMOMFGJ_00078 | 2.5e-200 | yyaQ | S | YjbR | ||
BNMOMFGJ_00079 | 1.5e-118 | ccpA | K | Catabolite control protein A | ||
BNMOMFGJ_00080 | 1.7e-142 | P | molecular chaperone | |||
BNMOMFGJ_00081 | 2e-94 | XK27_05505 | S | Psort location CytoplasmicMembrane, score | ||
BNMOMFGJ_00083 | 4.1e-50 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
BNMOMFGJ_00084 | 1.4e-59 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
BNMOMFGJ_00085 | 1.8e-136 | 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 | |
BNMOMFGJ_00086 | 1.1e-130 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
BNMOMFGJ_00087 | 2.8e-108 | 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 | ||
BNMOMFGJ_00088 | 6.3e-96 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
BNMOMFGJ_00089 | 1.4e-163 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
BNMOMFGJ_00090 | 2.4e-105 | pilD | 3.4.23.43 | NOU | Type II secretory pathway prepilin signal peptidase PulO and related peptidases | |
BNMOMFGJ_00091 | 1.1e-89 | dps | P | Belongs to the Dps family | ||
BNMOMFGJ_00092 | 3.4e-79 | perR | P | Belongs to the Fur family | ||
BNMOMFGJ_00093 | 7.1e-27 | yqgQ | S | protein conserved in bacteria | ||
BNMOMFGJ_00094 | 7.1e-178 | glk | 2.7.1.2 | G | Glucokinase | |
BNMOMFGJ_00095 | 0.0 | typA | T | GTP-binding protein TypA | ||
BNMOMFGJ_00096 | 9.5e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
BNMOMFGJ_00097 | 5.2e-161 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
BNMOMFGJ_00098 | 1.3e-176 | cbiM | P | biosynthesis protein CbiM | ||
BNMOMFGJ_00099 | 1.1e-136 | P | cobalt transport protein | |||
BNMOMFGJ_00100 | 6.3e-131 | cbiO | P | ABC transporter | ||
BNMOMFGJ_00101 | 6.3e-138 | ET | ABC transporter substrate-binding protein | |||
BNMOMFGJ_00102 | 1.9e-164 | metQ | M | Belongs to the NlpA lipoprotein family | ||
BNMOMFGJ_00103 | 2.9e-30 | yggT | D | integral membrane protein | ||
BNMOMFGJ_00104 | 1.8e-99 | sepF | D | cell septum assembly | ||
BNMOMFGJ_00105 | 2.3e-122 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
BNMOMFGJ_00106 | 1.6e-233 | 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 | ||
BNMOMFGJ_00107 | 7.1e-224 | 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 | ||
BNMOMFGJ_00108 | 1.1e-129 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
BNMOMFGJ_00109 | 1.2e-199 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
BNMOMFGJ_00110 | 7.9e-20 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
BNMOMFGJ_00112 | 2.7e-147 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
BNMOMFGJ_00113 | 8.5e-08 | N | PFAM Uncharacterised protein family UPF0150 | |||
BNMOMFGJ_00114 | 4.5e-112 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
BNMOMFGJ_00115 | 7.1e-298 | 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 | ||
BNMOMFGJ_00116 | 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 | |
BNMOMFGJ_00117 | 1.7e-18 | S | Domain of unknown function (DUF4649) | |||
BNMOMFGJ_00118 | 2.8e-177 | XK27_08835 | S | ABC transporter substrate binding protein | ||
BNMOMFGJ_00119 | 2.6e-147 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
BNMOMFGJ_00120 | 6.8e-136 | XK27_08845 | S | abc transporter atp-binding protein | ||
BNMOMFGJ_00121 | 6e-310 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
BNMOMFGJ_00122 | 3.6e-148 | estA | CE1 | S | Esterase | |
BNMOMFGJ_00123 | 9.2e-112 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
BNMOMFGJ_00124 | 3.6e-276 | 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 | |
BNMOMFGJ_00125 | 7.9e-37 | ysdA | L | Membrane | ||
BNMOMFGJ_00126 | 1.9e-189 | 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 | |
BNMOMFGJ_00127 | 1.2e-288 | 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) | |
BNMOMFGJ_00128 | 7.2e-39 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
BNMOMFGJ_00129 | 3.7e-108 | yeaB | K | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
BNMOMFGJ_00130 | 2.8e-249 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNMOMFGJ_00131 | 3.8e-182 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNMOMFGJ_00132 | 1e-156 | rssA | S | Phospholipase, patatin family | ||
BNMOMFGJ_00133 | 2.4e-102 | estA | E | Lysophospholipase L1 and related esterases | ||
BNMOMFGJ_00134 | 3e-201 | S | unusual protein kinase | |||
BNMOMFGJ_00135 | 2.4e-08 | S | Enterocin A Immunity | |||
BNMOMFGJ_00136 | 2.2e-193 | mccF | V | LD-carboxypeptidase | ||
BNMOMFGJ_00137 | 2.1e-15 | S | integral membrane protein | |||
BNMOMFGJ_00138 | 1.1e-43 | czrA | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BNMOMFGJ_00139 | 5.1e-120 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
BNMOMFGJ_00140 | 7.4e-157 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
BNMOMFGJ_00142 | 9e-75 | XK27_03180 | T | universal stress protein | ||
BNMOMFGJ_00143 | 7.6e-238 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
BNMOMFGJ_00144 | 8.1e-140 | 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 | ||
BNMOMFGJ_00145 | 4.4e-100 | pncA | Q | isochorismatase | ||
BNMOMFGJ_00146 | 2e-71 | lytE | M | LysM domain protein | ||
BNMOMFGJ_00147 | 1.3e-132 | 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 | ||
BNMOMFGJ_00148 | 2.1e-154 | 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 | |
BNMOMFGJ_00149 | 8.3e-151 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
BNMOMFGJ_00150 | 4.1e-90 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
BNMOMFGJ_00151 | 4.4e-131 | S | sequence-specific DNA binding | |||
BNMOMFGJ_00152 | 1.1e-92 | ymfH | S | Peptidase M16 | ||
BNMOMFGJ_00153 | 1.3e-65 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
BNMOMFGJ_00154 | 4.9e-139 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
BNMOMFGJ_00155 | 1.1e-136 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
BNMOMFGJ_00156 | 1.6e-123 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
BNMOMFGJ_00157 | 2.3e-111 | acuB | S | CBS domain | ||
BNMOMFGJ_00158 | 6.3e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
BNMOMFGJ_00159 | 4.2e-107 | yvyE | 3.4.13.9 | S | YigZ family | |
BNMOMFGJ_00160 | 1.2e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
BNMOMFGJ_00161 | 6.6e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
BNMOMFGJ_00162 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
BNMOMFGJ_00163 | 1.3e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
BNMOMFGJ_00164 | 1.9e-23 | rpmD | J | ribosomal protein l30 | ||
BNMOMFGJ_00165 | 5.7e-58 | rplO | J | binds to the 23S rRNA | ||
BNMOMFGJ_00166 | 2.1e-230 | 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 | ||
BNMOMFGJ_00167 | 2.1e-114 | 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 | |
BNMOMFGJ_00168 | 2.7e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
BNMOMFGJ_00169 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
BNMOMFGJ_00170 | 4e-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 | ||
BNMOMFGJ_00171 | 1.9e-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 | ||
BNMOMFGJ_00172 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BNMOMFGJ_00173 | 4.4e-62 | rplQ | J | ribosomal protein l17 | ||
BNMOMFGJ_00174 | 1.6e-241 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
BNMOMFGJ_00176 | 4.8e-165 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
BNMOMFGJ_00177 | 5e-198 | L | DNA integration | |||
BNMOMFGJ_00178 | 4e-16 | |||||
BNMOMFGJ_00179 | 4.8e-170 | isp2 | S | pathogenesis | ||
BNMOMFGJ_00180 | 4.4e-30 | |||||
BNMOMFGJ_00181 | 6.4e-260 | |||||
BNMOMFGJ_00182 | 0.0 | yddE | S | AAA-like domain | ||
BNMOMFGJ_00183 | 1.2e-70 | S | TcpE family | |||
BNMOMFGJ_00184 | 3.2e-33 | |||||
BNMOMFGJ_00185 | 9.5e-162 | S | Conjugative transposon protein TcpC | |||
BNMOMFGJ_00186 | 2.3e-88 | |||||
BNMOMFGJ_00187 | 4.3e-33 | |||||
BNMOMFGJ_00188 | 4.9e-224 | K | Replication initiation factor | |||
BNMOMFGJ_00189 | 6.8e-277 | ydcQ | D | Ftsk spoiiie family protein | ||
BNMOMFGJ_00190 | 6.6e-73 | |||||
BNMOMFGJ_00191 | 1.7e-42 | |||||
BNMOMFGJ_00193 | 4e-46 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
BNMOMFGJ_00194 | 1.1e-14 | O | Restriction endonuclease | |||
BNMOMFGJ_00195 | 7.8e-128 | E | IrrE N-terminal-like domain | |||
BNMOMFGJ_00196 | 1.4e-111 | K | Peptidase S24-like protein | |||
BNMOMFGJ_00197 | 4.8e-201 | 2.7.13.3 | T | protein histidine kinase activity | ||
BNMOMFGJ_00198 | 2.6e-124 | agrA | KT | phosphorelay signal transduction system | ||
BNMOMFGJ_00199 | 1.1e-157 | O | protein import | |||
BNMOMFGJ_00200 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BNMOMFGJ_00201 | 2.6e-155 | pstS | P | phosphate | ||
BNMOMFGJ_00202 | 1.2e-252 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
BNMOMFGJ_00203 | 5.9e-143 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
BNMOMFGJ_00204 | 1e-44 | yktA | S | Belongs to the UPF0223 family | ||
BNMOMFGJ_00205 | 7.2e-71 | 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 | |
BNMOMFGJ_00206 | 1.6e-171 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
BNMOMFGJ_00207 | 2.3e-90 | niaR | S | small molecule binding protein (contains 3H domain) | ||
BNMOMFGJ_00208 | 2.7e-86 | |||||
BNMOMFGJ_00209 | 1.7e-274 | 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 | |
BNMOMFGJ_00210 | 2e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
BNMOMFGJ_00211 | 7.7e-126 | gntR1 | K | transcriptional | ||
BNMOMFGJ_00212 | 5.6e-99 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
BNMOMFGJ_00213 | 2.4e-133 | fecE | 3.6.3.34 | HP | ABC transporter | |
BNMOMFGJ_00214 | 4.7e-172 | fatB | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
BNMOMFGJ_00215 | 7.1e-124 | ybbA | S | Putative esterase | ||
BNMOMFGJ_00216 | 1.7e-48 | |||||
BNMOMFGJ_00217 | 9.8e-127 | V | CAAX protease self-immunity | |||
BNMOMFGJ_00218 | 2.6e-10 | |||||
BNMOMFGJ_00219 | 6.5e-19 | M | Bacterial lipoprotein | |||
BNMOMFGJ_00223 | 5.8e-146 | V | Psort location CytoplasmicMembrane, score | |||
BNMOMFGJ_00225 | 1.3e-287 | O | MreB/Mbl protein | |||
BNMOMFGJ_00226 | 1.9e-124 | V | abc transporter atp-binding protein | |||
BNMOMFGJ_00227 | 0.0 | V | ABC transporter (Permease | |||
BNMOMFGJ_00228 | 1e-120 | K | transcriptional regulator, MerR family | |||
BNMOMFGJ_00229 | 1.2e-158 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
BNMOMFGJ_00230 | 1.7e-76 | ypmB | S | Protein conserved in bacteria | ||
BNMOMFGJ_00231 | 1.2e-211 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
BNMOMFGJ_00232 | 3.2e-261 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
BNMOMFGJ_00233 | 2.2e-19 | |||||
BNMOMFGJ_00234 | 2.3e-63 | tdcF | 3.5.99.10 | J | endoribonuclease L-PSP | |
BNMOMFGJ_00235 | 1.9e-167 | XK27_01785 | S | cog cog1284 | ||
BNMOMFGJ_00236 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
BNMOMFGJ_00238 | 2.5e-239 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
BNMOMFGJ_00239 | 6.2e-32 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
BNMOMFGJ_00240 | 3.1e-11 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
BNMOMFGJ_00241 | 4.3e-22 | |||||
BNMOMFGJ_00242 | 2e-217 | EGP | Transmembrane secretion effector | |||
BNMOMFGJ_00243 | 1e-257 | yheS_2 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
BNMOMFGJ_00244 | 1.1e-49 | |||||
BNMOMFGJ_00245 | 8.7e-60 | |||||
BNMOMFGJ_00246 | 5.9e-55 | |||||
BNMOMFGJ_00247 | 1.5e-36 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
BNMOMFGJ_00248 | 7.9e-58 | 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 | |
BNMOMFGJ_00249 | 1e-85 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
BNMOMFGJ_00250 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
BNMOMFGJ_00251 | 1.5e-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 | ||
BNMOMFGJ_00252 | 8.5e-84 | XK27_03610 | K | Gnat family | ||
BNMOMFGJ_00253 | 1.9e-92 | yybC | ||||
BNMOMFGJ_00254 | 4.9e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
BNMOMFGJ_00255 | 3.2e-272 | pepV | 3.5.1.18 | E | Dipeptidase | |
BNMOMFGJ_00256 | 7.1e-148 | clcA_2 | P | Chloride transporter, ClC family | ||
BNMOMFGJ_00257 | 5.2e-133 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
BNMOMFGJ_00258 | 4e-130 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
BNMOMFGJ_00259 | 1.4e-249 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BNMOMFGJ_00260 | 6.8e-133 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
BNMOMFGJ_00261 | 3.3e-107 | recN | L | May be involved in recombinational repair of damaged DNA | ||
BNMOMFGJ_00262 | 1.7e-148 | DegV | S | DegV family | ||
BNMOMFGJ_00263 | 1.3e-154 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
BNMOMFGJ_00264 | 1.8e-96 | ypmS | S | Protein conserved in bacteria | ||
BNMOMFGJ_00265 | 6.3e-39 | 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 | ||
BNMOMFGJ_00267 | 3.1e-178 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
BNMOMFGJ_00268 | 2.1e-114 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
BNMOMFGJ_00269 | 2.3e-168 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
BNMOMFGJ_00270 | 2.3e-177 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
BNMOMFGJ_00271 | 6.6e-279 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
BNMOMFGJ_00272 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BNMOMFGJ_00273 | 1e-187 | 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 | |
BNMOMFGJ_00274 | 2.7e-277 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
BNMOMFGJ_00275 | 7.5e-236 | 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 | |
BNMOMFGJ_00276 | 6.1e-77 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
BNMOMFGJ_00277 | 1.4e-153 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
BNMOMFGJ_00278 | 7.3e-248 | msrR | K | Transcriptional regulator | ||
BNMOMFGJ_00279 | 2.4e-151 | ydiA | P | C4-dicarboxylate transporter malic acid transport | ||
BNMOMFGJ_00280 | 3.1e-178 | cbf | S | 3'-5' exoribonuclease yhaM | ||
BNMOMFGJ_00281 | 2.5e-170 | rmuC | S | RmuC domain protein | ||
BNMOMFGJ_00282 | 1.1e-115 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
BNMOMFGJ_00283 | 7.8e-120 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
BNMOMFGJ_00284 | 1.2e-160 | rsgA | 3.1.3.100 | G | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
BNMOMFGJ_00286 | 1.5e-77 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
BNMOMFGJ_00287 | 2.5e-124 | 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 | |
BNMOMFGJ_00288 | 6.6e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
BNMOMFGJ_00289 | 1.1e-198 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
BNMOMFGJ_00290 | 6.8e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
BNMOMFGJ_00291 | 2.4e-44 | 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 | ||
BNMOMFGJ_00292 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
BNMOMFGJ_00293 | 2.4e-110 | 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 | ||
BNMOMFGJ_00294 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
BNMOMFGJ_00295 | 3.9e-187 | 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 | |
BNMOMFGJ_00296 | 8.7e-125 | XK27_09800 | I | Acyltransferase | ||
BNMOMFGJ_00297 | 1.4e-158 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
BNMOMFGJ_00298 | 0.0 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
BNMOMFGJ_00299 | 5.3e-162 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
BNMOMFGJ_00300 | 1.5e-72 | adcB | P | ABC transporter (Permease | ||
BNMOMFGJ_00301 | 3e-183 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
BNMOMFGJ_00302 | 2e-124 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
BNMOMFGJ_00303 | 4.8e-18 | S | Protein of unknown function (DUF3021) | |||
BNMOMFGJ_00304 | 1.5e-152 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
BNMOMFGJ_00305 | 1.6e-282 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
BNMOMFGJ_00306 | 2.9e-178 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | glucose-1-phosphate adenylyltransferase |
BNMOMFGJ_00307 | 1e-188 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
BNMOMFGJ_00308 | 1.5e-73 | 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 |
BNMOMFGJ_00311 | 4.9e-102 | C | radical SAM domain protein | |||
BNMOMFGJ_00312 | 3.6e-143 | H | Outer membrane protein beta-barrel family | |||
BNMOMFGJ_00313 | 2.3e-119 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNMOMFGJ_00314 | 2e-149 | S | TraX protein | |||
BNMOMFGJ_00316 | 1.3e-51 | V | ABC-2 family transporter protein | |||
BNMOMFGJ_00317 | 5.1e-82 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
BNMOMFGJ_00318 | 2.3e-142 | 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 | |
BNMOMFGJ_00319 | 6.3e-73 | argR | K | Regulates arginine biosynthesis genes | ||
BNMOMFGJ_00320 | 1.9e-147 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
BNMOMFGJ_00321 | 3.4e-155 | 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 | |
BNMOMFGJ_00322 | 4.6e-29 | 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 | |
BNMOMFGJ_00323 | 1.1e-234 | 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 | |
BNMOMFGJ_00325 | 7.6e-280 | XK27_00515 | D | Cell surface antigen C-terminus | ||
BNMOMFGJ_00327 | 6.1e-224 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BNMOMFGJ_00328 | 3e-133 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
BNMOMFGJ_00329 | 1.9e-72 | mgrA | K | Transcriptional regulator, MarR family | ||
BNMOMFGJ_00330 | 9.1e-145 | 1.6.5.2 | GM | NmrA-like family | ||
BNMOMFGJ_00331 | 7e-130 | proV | E | abc transporter atp-binding protein | ||
BNMOMFGJ_00332 | 6.3e-290 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
BNMOMFGJ_00333 | 1.4e-133 | S | double-stranded DNA endodeoxyribonuclease activity | |||
BNMOMFGJ_00335 | 1.2e-206 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
BNMOMFGJ_00336 | 6.6e-184 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
BNMOMFGJ_00337 | 6.4e-182 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
BNMOMFGJ_00338 | 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) | |
BNMOMFGJ_00339 | 3e-38 | ptsH | G | phosphocarrier protein Hpr | ||
BNMOMFGJ_00340 | 4.3e-222 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
BNMOMFGJ_00342 | 5.1e-165 | S | CAAX amino terminal protease family protein | |||
BNMOMFGJ_00343 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
BNMOMFGJ_00344 | 2.5e-62 | glnR | K | Transcriptional regulator | ||
BNMOMFGJ_00345 | 3e-87 | S | Fusaric acid resistance protein-like | |||
BNMOMFGJ_00346 | 5.8e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
BNMOMFGJ_00347 | 1.5e-86 | |||||
BNMOMFGJ_00348 | 4e-119 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BNMOMFGJ_00349 | 4.6e-118 | 2.4.1.21 | GT5 | M | Right handed beta helix region | |
BNMOMFGJ_00350 | 3.2e-173 | spd | F | DNA RNA non-specific endonuclease | ||
BNMOMFGJ_00351 | 7.7e-92 | lemA | S | LemA family | ||
BNMOMFGJ_00352 | 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 | ||
BNMOMFGJ_00353 | 3.9e-81 | 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 | ||
BNMOMFGJ_00354 | 2.3e-69 | 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 | ||
BNMOMFGJ_00355 | 4e-142 | purR | 2.4.2.7 | F | operon repressor | |
BNMOMFGJ_00356 | 6.4e-306 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BNMOMFGJ_00357 | 5.1e-237 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
BNMOMFGJ_00358 | 1.2e-35 | XK27_02060 | S | Transglycosylase associated protein | ||
BNMOMFGJ_00359 | 2.6e-71 | badR | K | Transcriptional regulator, marr family | ||
BNMOMFGJ_00360 | 3.2e-95 | S | reductase | |||
BNMOMFGJ_00362 | 1.3e-70 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
BNMOMFGJ_00363 | 3.7e-179 | scrR | K | Transcriptional regulator | ||
BNMOMFGJ_00364 | 1.5e-288 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
BNMOMFGJ_00365 | 4e-07 | |||||
BNMOMFGJ_00366 | 1e-136 | agrA | KT | response regulator | ||
BNMOMFGJ_00367 | 0.0 | 3.4.17.14, 3.5.1.28 | NU | GBS Bsp-like repeat | ||
BNMOMFGJ_00368 | 8.2e-210 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
BNMOMFGJ_00369 | 5.8e-160 | S | reductase | |||
BNMOMFGJ_00370 | 4.7e-168 | K | transcriptional regulator (lysR family) | |||
BNMOMFGJ_00371 | 8.5e-107 | S | CAAX amino terminal protease family protein | |||
BNMOMFGJ_00372 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
BNMOMFGJ_00373 | 3.1e-145 | XK27_08360 | S | EDD domain protein, DegV family | ||
BNMOMFGJ_00374 | 3.9e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
BNMOMFGJ_00375 | 3.9e-218 | 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 | |
BNMOMFGJ_00376 | 2.1e-177 | nptA | P | COG1283 Na phosphate symporter | ||
BNMOMFGJ_00377 | 2.6e-211 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
BNMOMFGJ_00378 | 2.1e-219 | S | membrane | |||
BNMOMFGJ_00379 | 1.4e-99 | pvaA | M | lytic transglycosylase activity | ||
BNMOMFGJ_00380 | 1.9e-178 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
BNMOMFGJ_00381 | 2.7e-230 | 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 | |
BNMOMFGJ_00382 | 4.5e-106 | 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 | |
BNMOMFGJ_00383 | 1.2e-32 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
BNMOMFGJ_00386 | 7.6e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
BNMOMFGJ_00387 | 1.9e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
BNMOMFGJ_00388 | 3e-187 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
BNMOMFGJ_00389 | 6.5e-125 | dnaD | ||||
BNMOMFGJ_00390 | 1.3e-181 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
BNMOMFGJ_00391 | 9.9e-94 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
BNMOMFGJ_00392 | 1.2e-285 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
BNMOMFGJ_00393 | 4.4e-77 | 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) | |
BNMOMFGJ_00394 | 1.3e-193 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
BNMOMFGJ_00395 | 2.2e-76 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
BNMOMFGJ_00396 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
BNMOMFGJ_00397 | 2.8e-64 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
BNMOMFGJ_00398 | 9.3e-36 | S | Helix-turn-helix domain | |||
BNMOMFGJ_00399 | 1.8e-30 | xis | S | Excisionase from transposon Tn916 | ||
BNMOMFGJ_00400 | 1.3e-232 | L | DNA binding domain of tn916 integrase | |||
BNMOMFGJ_00401 | 2.3e-54 | glnB | K | Belongs to the P(II) protein family | ||
BNMOMFGJ_00402 | 2e-222 | amt | P | Ammonium Transporter | ||
BNMOMFGJ_00403 | 9.2e-109 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
BNMOMFGJ_00404 | 3.4e-103 | kcsA | P | Ion transport protein | ||
BNMOMFGJ_00405 | 5.6e-116 | yvqF | S | Membrane | ||
BNMOMFGJ_00406 | 1.9e-170 | vraS | 2.7.13.3 | T | Histidine kinase | |
BNMOMFGJ_00407 | 1.4e-113 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
BNMOMFGJ_00408 | 7.3e-16 | S | Helix-turn-helix domain | |||
BNMOMFGJ_00409 | 2.9e-15 | S | Transcription factor WhiB | |||
BNMOMFGJ_00410 | 8.1e-17 | parA | D | VirC1 protein | ||
BNMOMFGJ_00411 | 4.5e-22 | |||||
BNMOMFGJ_00412 | 5.8e-43 | |||||
BNMOMFGJ_00413 | 1.2e-239 | V | ABC transporter | |||
BNMOMFGJ_00414 | 6.1e-126 | yeeN | K | transcriptional regulatory protein | ||
BNMOMFGJ_00415 | 5.9e-47 | yajC | U | protein transport | ||
BNMOMFGJ_00416 | 5.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BNMOMFGJ_00417 | 8.3e-227 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
BNMOMFGJ_00418 | 1.6e-105 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
BNMOMFGJ_00419 | 1e-102 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
BNMOMFGJ_00421 | 1.2e-34 | 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 | ||
BNMOMFGJ_00422 | 1.9e-62 | manO | S | protein conserved in bacteria | ||
BNMOMFGJ_00423 | 3.3e-169 | manN | G | PTS system mannose fructose sorbose family IID component | ||
BNMOMFGJ_00424 | 1.3e-116 | manM | G | pts system | ||
BNMOMFGJ_00425 | 4.9e-174 | manL | 2.7.1.191 | G | pts system | |
BNMOMFGJ_00426 | 7.7e-67 | manO | S | Protein conserved in bacteria | ||
BNMOMFGJ_00427 | 1.2e-85 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
BNMOMFGJ_00428 | 2e-42 | S | Sugar efflux transporter for intercellular exchange | |||
BNMOMFGJ_00429 | 1.7e-202 | P | FtsX-like permease family | |||
BNMOMFGJ_00430 | 1.1e-121 | V | abc transporter atp-binding protein | |||
BNMOMFGJ_00431 | 8.1e-97 | K | WHG domain | |||
BNMOMFGJ_00432 | 1e-93 | ydhF | S | Aldo keto reductase | ||
BNMOMFGJ_00433 | 7e-124 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
BNMOMFGJ_00434 | 4.8e-157 | H | COG0463 Glycosyltransferases involved in cell wall biogenesis | |||
BNMOMFGJ_00435 | 9.1e-189 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | |||
BNMOMFGJ_00436 | 7.2e-133 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
BNMOMFGJ_00437 | 1.1e-98 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
BNMOMFGJ_00438 | 8.4e-229 | 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 | |
BNMOMFGJ_00439 | 7.8e-143 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
BNMOMFGJ_00440 | 1.7e-230 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
BNMOMFGJ_00441 | 2.6e-150 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
BNMOMFGJ_00442 | 4.2e-210 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
BNMOMFGJ_00444 | 6.4e-30 | KT | response to antibiotic | |||
BNMOMFGJ_00445 | 7.7e-216 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
BNMOMFGJ_00446 | 6.7e-12 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
BNMOMFGJ_00447 | 5.8e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
BNMOMFGJ_00448 | 7.2e-130 | fasA | KT | Response regulator of the LytR AlgR family | ||
BNMOMFGJ_00449 | 2.2e-152 | fasC | T | protein histidine kinase activity | ||
BNMOMFGJ_00450 | 2.4e-104 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
BNMOMFGJ_00451 | 9.1e-42 | WQ51_02910 | S | Protein of unknown function, DUF536 | ||
BNMOMFGJ_00452 | 9.6e-64 | XK27_02560 | S | cog cog2151 | ||
BNMOMFGJ_00453 | 3.7e-61 | |||||
BNMOMFGJ_00454 | 3.8e-251 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
BNMOMFGJ_00455 | 4.1e-219 | 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 | |
BNMOMFGJ_00456 | 1.1e-184 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
BNMOMFGJ_00457 | 1.1e-251 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
BNMOMFGJ_00458 | 2.4e-16 | 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 | ||
BNMOMFGJ_00459 | 9e-122 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
BNMOMFGJ_00460 | 1.6e-77 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
BNMOMFGJ_00461 | 3.9e-85 | 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 | ||
BNMOMFGJ_00462 | 1e-279 | 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 | |
BNMOMFGJ_00463 | 1.1e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
BNMOMFGJ_00464 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
BNMOMFGJ_00465 | 3e-114 | papP | P | ABC transporter (Permease | ||
BNMOMFGJ_00466 | 9.3e-192 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
BNMOMFGJ_00467 | 1.4e-30 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
BNMOMFGJ_00468 | 1e-172 | copA | 3.6.3.54 | P | P-type ATPase | |
BNMOMFGJ_00471 | 3.9e-165 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
BNMOMFGJ_00472 | 1.6e-103 | S | Domain of unknown function (DUF1803) | |||
BNMOMFGJ_00473 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
BNMOMFGJ_00474 | 3.1e-136 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
BNMOMFGJ_00475 | 6.7e-99 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
BNMOMFGJ_00476 | 2.7e-123 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNMOMFGJ_00477 | 2e-164 | T | Histidine kinase | |||
BNMOMFGJ_00478 | 3.3e-308 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
BNMOMFGJ_00479 | 6.8e-134 | S | TraX protein | |||
BNMOMFGJ_00480 | 1e-38 | 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 | ||
BNMOMFGJ_00481 | 2.3e-262 | 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 | |
BNMOMFGJ_00482 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
BNMOMFGJ_00483 | 2.1e-217 | ftsW | D | Belongs to the SEDS family | ||
BNMOMFGJ_00484 | 2.3e-139 | S | SseB protein N-terminal domain | |||
BNMOMFGJ_00485 | 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 | |
BNMOMFGJ_00486 | 1e-69 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
BNMOMFGJ_00487 | 1.1e-184 | 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 | |
BNMOMFGJ_00488 | 1.9e-217 | 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 | |
BNMOMFGJ_00489 | 3.9e-128 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
BNMOMFGJ_00490 | 3.6e-46 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
BNMOMFGJ_00491 | 8.8e-113 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
BNMOMFGJ_00492 | 7.8e-194 | 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) | ||
BNMOMFGJ_00493 | 2.2e-128 | 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 | |
BNMOMFGJ_00494 | 5e-148 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
BNMOMFGJ_00495 | 1.4e-72 | yhaI | S | Protein of unknown function (DUF805) | ||
BNMOMFGJ_00496 | 4.1e-253 | pepC | 3.4.22.40 | E | aminopeptidase | |
BNMOMFGJ_00497 | 3.8e-34 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BNMOMFGJ_00498 | 1.5e-59 | 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 | |
BNMOMFGJ_00499 | 4.1e-93 | panT | S | ECF transporter, substrate-specific component | ||
BNMOMFGJ_00500 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
BNMOMFGJ_00501 | 1.6e-165 | metF | 1.5.1.20 | E | reductase | |
BNMOMFGJ_00502 | 1.1e-102 | |||||
BNMOMFGJ_00503 | 1.4e-113 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
BNMOMFGJ_00504 | 8.1e-95 | S | CAAX protease self-immunity | |||
BNMOMFGJ_00505 | 1.5e-49 | |||||
BNMOMFGJ_00507 | 2e-64 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
BNMOMFGJ_00508 | 7.1e-60 | S | Protein of unknown function (DUF1722) | |||
BNMOMFGJ_00509 | 4.9e-298 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
BNMOMFGJ_00510 | 8.6e-10 | S | D-Ala-teichoic acid biosynthesis protein | |||
BNMOMFGJ_00511 | 6.9e-198 | XK27_10035 | V | abc transporter atp-binding protein | ||
BNMOMFGJ_00512 | 1.4e-153 | malF | P | ABC transporter (Permease | ||
BNMOMFGJ_00513 | 9.8e-152 | malG | P | ABC transporter (Permease | ||
BNMOMFGJ_00514 | 4.7e-213 | msmX | P | Belongs to the ABC transporter superfamily | ||
BNMOMFGJ_00515 | 9.5e-23 | 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 | ||
BNMOMFGJ_00516 | 1.9e-51 | 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 | ||
BNMOMFGJ_00517 | 1.4e-113 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
BNMOMFGJ_00518 | 1.1e-158 | 5.2.1.8 | G | hydrolase | ||
BNMOMFGJ_00519 | 6.8e-27 | P | Hemerythrin HHE cation binding domain protein | |||
BNMOMFGJ_00520 | 2.3e-138 | XK27_00880 | 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
BNMOMFGJ_00521 | 5.2e-229 | 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 | ||
BNMOMFGJ_00522 | 1.3e-70 | 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 | ||
BNMOMFGJ_00525 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BNMOMFGJ_00526 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
BNMOMFGJ_00527 | 6.4e-194 | yhjX | P | Major Facilitator | ||
BNMOMFGJ_00528 | 1.3e-111 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
BNMOMFGJ_00529 | 3.3e-112 | 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 | |
BNMOMFGJ_00530 | 9.6e-237 | EGP | Major facilitator Superfamily | |||
BNMOMFGJ_00531 | 4e-66 | rmaI | K | Transcriptional regulator, MarR family | ||
BNMOMFGJ_00532 | 1.1e-87 | maa | 2.3.1.79 | GK | Maltose O-acetyltransferase | |
BNMOMFGJ_00533 | 2.2e-18 | XK27_08880 | ||||
BNMOMFGJ_00534 | 1e-75 | fld | C | Flavodoxin | ||
BNMOMFGJ_00535 | 8.3e-282 | clcA | P | Chloride transporter, ClC family | ||
BNMOMFGJ_00536 | 5.6e-40 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
BNMOMFGJ_00537 | 4.6e-282 | 3.1.4.37 | T | RNA ligase | ||
BNMOMFGJ_00538 | 5.8e-161 | S | phosphoesterase or phosphohydrolase | |||
BNMOMFGJ_00539 | 8.9e-130 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
BNMOMFGJ_00540 | 8.1e-30 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BNMOMFGJ_00541 | 9.2e-184 | 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 | |
BNMOMFGJ_00542 | 1.4e-139 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
BNMOMFGJ_00543 | 9.6e-74 | araT | 2.6.1.1 | E | Aminotransferase | |
BNMOMFGJ_00544 | 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 | |
BNMOMFGJ_00545 | 2.8e-85 | ccl | S | cog cog4708 | ||
BNMOMFGJ_00546 | 5.5e-78 | rbn | E | Belongs to the UPF0761 family | ||
BNMOMFGJ_00548 | 5.4e-156 | XK27_03015 | S | permease | ||
BNMOMFGJ_00549 | 6.4e-148 | ycgQ | S | TIGR03943 family | ||
BNMOMFGJ_00550 | 1.7e-28 | sulP | P | Sulfate permease and related transporters (MFS superfamily) | ||
BNMOMFGJ_00551 | 4.9e-39 | S | granule-associated protein | |||
BNMOMFGJ_00552 | 1.8e-286 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BNMOMFGJ_00553 | 8.3e-100 | S | hmm pf01594 | |||
BNMOMFGJ_00554 | 0.0 | ydaO | E | amino acid | ||
BNMOMFGJ_00555 | 7.7e-100 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
BNMOMFGJ_00556 | 1.1e-144 | 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 | |
BNMOMFGJ_00558 | 5.8e-162 | T | Diguanylate cyclase | |||
BNMOMFGJ_00559 | 2.2e-35 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
BNMOMFGJ_00560 | 1.7e-60 | fruR | K | transcriptional | ||
BNMOMFGJ_00561 | 2.5e-28 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
BNMOMFGJ_00562 | 5.7e-25 | L | Transposase | |||
BNMOMFGJ_00563 | 5.6e-112 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
BNMOMFGJ_00564 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
BNMOMFGJ_00565 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
BNMOMFGJ_00566 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
BNMOMFGJ_00567 | 6.6e-08 | |||||
BNMOMFGJ_00568 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
BNMOMFGJ_00569 | 3.1e-78 | feoA | P | FeoA domain protein | ||
BNMOMFGJ_00570 | 1.3e-41 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
BNMOMFGJ_00571 | 2.8e-210 | arcT | 2.6.1.1 | E | Aminotransferase | |
BNMOMFGJ_00572 | 2.2e-137 | ET | Belongs to the bacterial solute-binding protein 3 family | |||
BNMOMFGJ_00573 | 2.4e-139 | ET | ABC transporter | |||
BNMOMFGJ_00574 | 3.3e-92 | tetR | K | transcriptional regulator | ||
BNMOMFGJ_00575 | 1.6e-123 | V | abc transporter atp-binding protein | |||
BNMOMFGJ_00576 | 1.6e-143 | XK27_04800 | S | Sucrose-6F-phosphate phosphohydrolase | ||
BNMOMFGJ_00577 | 1.3e-80 | S | Bacterial inner membrane protein | |||
BNMOMFGJ_00578 | 1.8e-113 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
BNMOMFGJ_00579 | 1.4e-147 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
BNMOMFGJ_00580 | 3.7e-168 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
BNMOMFGJ_00581 | 2.2e-41 | pspC | KT | PspC domain | ||
BNMOMFGJ_00582 | 2.5e-82 | ydcK | S | Belongs to the SprT family | ||
BNMOMFGJ_00583 | 2.8e-160 | yhgF | K | Transcriptional accessory protein | ||
BNMOMFGJ_00584 | 7.3e-189 | XK27_10075 | S | abc transporter atp-binding protein | ||
BNMOMFGJ_00585 | 0.0 | V | abc transporter atp-binding protein | |||
BNMOMFGJ_00586 | 4.3e-92 | V | abc transporter atp-binding protein | |||
BNMOMFGJ_00587 | 8.5e-154 | blt | G | MFS/sugar transport protein | ||
BNMOMFGJ_00588 | 2.6e-118 | K | transcriptional regulator | |||
BNMOMFGJ_00589 | 1.3e-248 | srfJ1 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain |
BNMOMFGJ_00590 | 1.2e-88 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
BNMOMFGJ_00591 | 2.7e-174 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
BNMOMFGJ_00592 | 1.9e-138 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
BNMOMFGJ_00593 | 6.2e-123 | Q | Methyltransferase domain | |||
BNMOMFGJ_00594 | 8e-67 | GnaT | 2.5.1.16 | K | acetyltransferase | |
BNMOMFGJ_00595 | 5.7e-211 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
BNMOMFGJ_00597 | 1.5e-39 | yjdF | S | Protein of unknown function (DUF2992) | ||
BNMOMFGJ_00598 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BNMOMFGJ_00600 | 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 |
BNMOMFGJ_00601 | 8.7e-121 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
BNMOMFGJ_00602 | 8.2e-41 | 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 | ||
BNMOMFGJ_00603 | 4.4e-129 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
BNMOMFGJ_00604 | 2.5e-121 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
BNMOMFGJ_00605 | 8.1e-126 | sitB | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
BNMOMFGJ_00606 | 1.2e-133 | mtsC | P | ABC-type Mn2 Zn2 transport systems, permease components | ||
BNMOMFGJ_00607 | 2.1e-171 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
BNMOMFGJ_00608 | 3.2e-118 | sirR | K | iron dependent repressor | ||
BNMOMFGJ_00609 | 0.0 | mdlA | V | abc transporter atp-binding protein | ||
BNMOMFGJ_00611 | 8e-227 | murN | 2.3.2.16 | V | FemAB family | |
BNMOMFGJ_00612 | 4.4e-118 | M | Pfam SNARE associated Golgi protein | |||
BNMOMFGJ_00613 | 1.9e-107 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
BNMOMFGJ_00616 | 1.1e-170 | 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 | |
BNMOMFGJ_00617 | 7.6e-252 | 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 | ||
BNMOMFGJ_00618 | 6.5e-183 | D | nuclear chromosome segregation | |||
BNMOMFGJ_00619 | 2.2e-123 | glnQ | E | abc transporter atp-binding protein | ||
BNMOMFGJ_00620 | 1.6e-42 | glnP | P | ABC transporter | ||
BNMOMFGJ_00621 | 7.6e-75 | S | Psort location CytoplasmicMembrane, score | |||
BNMOMFGJ_00622 | 5.6e-65 | S | Domain of unknown function (DUF4430) | |||
BNMOMFGJ_00623 | 3.8e-57 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
BNMOMFGJ_00624 | 1.4e-256 | noxE | P | NADH oxidase | ||
BNMOMFGJ_00625 | 1.4e-231 | yfmM | S | abc transporter atp-binding protein | ||
BNMOMFGJ_00626 | 1.5e-118 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
BNMOMFGJ_00627 | 7.1e-217 | ywbD | 2.1.1.191 | J | Methyltransferase | |
BNMOMFGJ_00628 | 2e-152 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
BNMOMFGJ_00629 | 8.2e-64 | 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 | ||
BNMOMFGJ_00630 | 1.8e-61 | yutD | J | protein conserved in bacteria | ||
BNMOMFGJ_00631 | 2.1e-255 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
BNMOMFGJ_00634 | 5.9e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
BNMOMFGJ_00635 | 2.6e-135 | yejC | S | cyclic nucleotide-binding protein | ||
BNMOMFGJ_00636 | 9.9e-187 | D | nuclear chromosome segregation | |||
BNMOMFGJ_00638 | 8.5e-252 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
BNMOMFGJ_00639 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
BNMOMFGJ_00640 | 1.8e-75 | ctsR | K | Belongs to the CtsR family | ||
BNMOMFGJ_00641 | 1.1e-161 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
BNMOMFGJ_00642 | 3.8e-54 | 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 | |
BNMOMFGJ_00643 | 9.7e-147 | 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 | ||
BNMOMFGJ_00645 | 4.8e-257 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
BNMOMFGJ_00646 | 2e-191 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
BNMOMFGJ_00647 | 4.6e-88 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BNMOMFGJ_00648 | 1.2e-186 | ylbL | T | Belongs to the peptidase S16 family | ||
BNMOMFGJ_00649 | 1.9e-86 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
BNMOMFGJ_00650 | 1.9e-92 | rsmD | 2.1.1.171 | L | Methyltransferase | |
BNMOMFGJ_00651 | 9.3e-29 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
BNMOMFGJ_00653 | 2.1e-232 | S | dextransucrase activity | |||
BNMOMFGJ_00654 | 2.4e-32 | pscB | M | CHAP domain protein | ||
BNMOMFGJ_00655 | 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 | ||
BNMOMFGJ_00656 | 1.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
BNMOMFGJ_00657 | 3.6e-41 | K | sequence-specific DNA binding | |||
BNMOMFGJ_00658 | 1.1e-128 | S | G5 | |||
BNMOMFGJ_00659 | 2e-56 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
BNMOMFGJ_00660 | 2.1e-44 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
BNMOMFGJ_00661 | 0.0 | S | Bacterial membrane protein, YfhO | |||
BNMOMFGJ_00662 | 8.7e-90 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
BNMOMFGJ_00663 | 6.6e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
BNMOMFGJ_00664 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
BNMOMFGJ_00665 | 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) | |
BNMOMFGJ_00666 | 2e-161 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
BNMOMFGJ_00667 | 2.9e-101 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
BNMOMFGJ_00668 | 4.5e-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 | |
BNMOMFGJ_00669 | 3.7e-82 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
BNMOMFGJ_00670 | 2.1e-168 | murB | 1.3.1.98 | M | cell wall formation | |
BNMOMFGJ_00671 | 3.2e-64 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
BNMOMFGJ_00672 | 6.3e-54 | K | transcriptional regulator, PadR family | |||
BNMOMFGJ_00673 | 1.7e-116 | nudL | L | hydrolase | ||
BNMOMFGJ_00675 | 2.4e-95 | XK27_06935 | K | transcriptional regulator | ||
BNMOMFGJ_00676 | 2.7e-53 | ypaA | M | Membrane | ||
BNMOMFGJ_00677 | 1.9e-10 | |||||
BNMOMFGJ_00678 | 3.1e-223 | G | COG0457 FOG TPR repeat | |||
BNMOMFGJ_00679 | 4.7e-176 | yubA | S | permease | ||
BNMOMFGJ_00680 | 2.1e-252 | ctpE | P | E1-E2 ATPase | ||
BNMOMFGJ_00681 | 5.3e-59 | |||||
BNMOMFGJ_00682 | 1.2e-40 | pchB | 2.5.1.19, 4.2.1.10, 4.2.99.21, 5.4.99.5 | E | Chorismate mutase type II | |
BNMOMFGJ_00683 | 5.7e-242 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
BNMOMFGJ_00684 | 4.5e-280 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
BNMOMFGJ_00685 | 1.4e-122 | 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 | |
BNMOMFGJ_00686 | 3e-198 | 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) | |
BNMOMFGJ_00687 | 4e-170 | lmrA | V | abc transporter atp-binding protein | ||
BNMOMFGJ_00688 | 2.9e-218 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
BNMOMFGJ_00689 | 1.5e-239 | metY | 2.5.1.49 | E | o-acetylhomoserine | |
BNMOMFGJ_00690 | 7.7e-118 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
BNMOMFGJ_00691 | 5.4e-24 | |||||
BNMOMFGJ_00692 | 5e-96 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
BNMOMFGJ_00693 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
BNMOMFGJ_00694 | 1.8e-44 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
BNMOMFGJ_00695 | 4.7e-91 | mmuP | E | amino acid | ||
BNMOMFGJ_00696 | 2.6e-161 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
BNMOMFGJ_00697 | 2.2e-30 | S | Domain of unknown function (DUF1912) | |||
BNMOMFGJ_00698 | 4.8e-13 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
BNMOMFGJ_00699 | 1.5e-44 | 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 | |
BNMOMFGJ_00700 | 2.4e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
BNMOMFGJ_00701 | 3e-259 | S | phospholipase Carboxylesterase | |||
BNMOMFGJ_00702 | 2.4e-133 | 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 | |
BNMOMFGJ_00703 | 1.2e-160 | prmA | J | Ribosomal protein L11 methyltransferase | ||
BNMOMFGJ_00704 | 4.6e-45 | L | RePlication protein | |||
BNMOMFGJ_00705 | 3.4e-36 | P | (belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family) | |||
BNMOMFGJ_00706 | 1.8e-279 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
BNMOMFGJ_00707 | 1.9e-150 | S | Domain of unknown function (DUF4300) | |||
BNMOMFGJ_00708 | 1.2e-124 | V | CAAX protease self-immunity | |||
BNMOMFGJ_00709 | 3e-93 | S | UPF0397 protein | |||
BNMOMFGJ_00710 | 3.8e-93 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
BNMOMFGJ_00711 | 1e-117 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
BNMOMFGJ_00712 | 5.9e-82 | nrdI | F | Belongs to the NrdI family | ||
BNMOMFGJ_00713 | 2.7e-168 | 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 | |
BNMOMFGJ_00714 | 2.4e-50 | trxA | O | Belongs to the thioredoxin family | ||
BNMOMFGJ_00715 | 7.2e-74 | yccU | S | CoA-binding protein | ||
BNMOMFGJ_00716 | 1.2e-143 | tatD | L | Hydrolase, tatd | ||
BNMOMFGJ_00717 | 1.1e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
BNMOMFGJ_00718 | 9.6e-29 | P | ABC transporter (Permease | |||
BNMOMFGJ_00719 | 1.5e-135 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
BNMOMFGJ_00720 | 7.4e-155 | cjaA | ET | ABC transporter substrate-binding protein | ||
BNMOMFGJ_00722 | 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 |
BNMOMFGJ_00723 | 4.9e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
BNMOMFGJ_00724 | 6.8e-142 | cmpC | S | abc transporter atp-binding protein | ||
BNMOMFGJ_00725 | 2.2e-118 | WQ51_06230 | S | ABC transporter substrate binding protein | ||
BNMOMFGJ_00726 | 7.6e-166 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
BNMOMFGJ_00727 | 5.1e-34 | S | Phenazine biosynthesis protein | |||
BNMOMFGJ_00728 | 2.2e-92 | 2.7.7.65 | T | Psort location CytoplasmicMembrane, score | ||
BNMOMFGJ_00729 | 3.7e-132 | cbiQ | P | Cobalt transport protein | ||
BNMOMFGJ_00730 | 1.3e-108 | 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 | ||
BNMOMFGJ_00731 | 4.4e-94 | ypsA | S | Belongs to the UPF0398 family | ||
BNMOMFGJ_00732 | 2e-132 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
BNMOMFGJ_00733 | 1.6e-39 | MA20_06245 | S | yiaA/B two helix domain | ||
BNMOMFGJ_00734 | 9.8e-60 | uup | S | abc transporter atp-binding protein | ||
BNMOMFGJ_00735 | 1.5e-261 | yloV | S | kinase related to dihydroxyacetone kinase | ||
BNMOMFGJ_00736 | 1.7e-117 | yoaK | S | Protein of unknown function (DUF1275) | ||
BNMOMFGJ_00737 | 2.3e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
BNMOMFGJ_00738 | 9.2e-207 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
BNMOMFGJ_00739 | 3.3e-150 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
BNMOMFGJ_00740 | 2.2e-43 | comGC | U | Required for transformation and DNA binding | ||
BNMOMFGJ_00741 | 1.4e-69 | cglD | NU | Competence protein | ||
BNMOMFGJ_00742 | 3.1e-15 | NU | Type II secretory pathway pseudopilin | |||
BNMOMFGJ_00743 | 4.5e-71 | comGF | U | Competence protein ComGF | ||
BNMOMFGJ_00744 | 4.4e-12 | comGF | U | Putative Competence protein ComGF | ||
BNMOMFGJ_00745 | 4e-45 | ftsL | D | cell division protein FtsL | ||
BNMOMFGJ_00746 | 2.6e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
BNMOMFGJ_00747 | 1.3e-95 | |||||
BNMOMFGJ_00748 | 7.7e-41 | K | DNA-binding helix-turn-helix protein | |||
BNMOMFGJ_00749 | 7.2e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
BNMOMFGJ_00750 | 1.3e-134 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BNMOMFGJ_00751 | 2.2e-25 | GK | ROK family | |||
BNMOMFGJ_00752 | 3.1e-295 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BNMOMFGJ_00753 | 1e-56 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
BNMOMFGJ_00754 | 4e-170 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
BNMOMFGJ_00755 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
BNMOMFGJ_00756 | 3e-173 | 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 | ||
BNMOMFGJ_00758 | 1.2e-186 | phoH | T | phosphate starvation-inducible protein PhoH | ||
BNMOMFGJ_00759 | 1.5e-71 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
BNMOMFGJ_00760 | 5.6e-54 | 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 | |
BNMOMFGJ_00761 | 2.6e-233 | 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 | |
BNMOMFGJ_00762 | 1.6e-44 | yoeB | S | Addiction module toxin, Txe YoeB family | ||
BNMOMFGJ_00763 | 3.4e-39 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
BNMOMFGJ_00764 | 1.5e-43 | ylbM | S | Belongs to the UPF0348 family | ||
BNMOMFGJ_00765 | 1.1e-222 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
BNMOMFGJ_00766 | 3.3e-200 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
BNMOMFGJ_00767 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
BNMOMFGJ_00768 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
BNMOMFGJ_00769 | 1.9e-92 | 2.3.1.128 | K | acetyltransferase | ||
BNMOMFGJ_00770 | 4.4e-230 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
BNMOMFGJ_00771 | 6.9e-156 | 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 | |
BNMOMFGJ_00772 | 1.5e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
BNMOMFGJ_00773 | 1.5e-219 | metE | 2.1.1.14 | E | Methionine synthase | |
BNMOMFGJ_00774 | 4.9e-93 | yabB | 2.1.1.223 | L | Methyltransferase | |
BNMOMFGJ_00775 | 2.5e-40 | yazA | L | endonuclease containing a URI domain | ||
BNMOMFGJ_00776 | 8.7e-28 | vanY | 3.4.17.14, 3.5.1.28 | M | D-alanyl-D-alanine carboxypeptidase | |
BNMOMFGJ_00777 | 1.6e-21 | 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 | |
BNMOMFGJ_00778 | 2.9e-209 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
BNMOMFGJ_00779 | 9.2e-234 | G | beta-galactosidase activity | |||
BNMOMFGJ_00780 | 1.5e-71 | G | Bacterial extracellular solute-binding protein | |||
BNMOMFGJ_00781 | 3.5e-39 | IQ | KR domain | |||
BNMOMFGJ_00782 | 9.2e-195 | S | Fic/DOC family | |||
BNMOMFGJ_00783 | 3.6e-78 | U | Binding-protein-dependent transport system inner membrane component | |||
BNMOMFGJ_00784 | 6.3e-242 | G | Bacterial extracellular solute-binding protein | |||
BNMOMFGJ_00785 | 9.1e-195 | abf | G | Glycosyl hydrolases family 43 | ||
BNMOMFGJ_00786 | 2e-85 | I | alpha/beta hydrolase fold | |||
BNMOMFGJ_00787 | 1.4e-163 | K | helix_turn _helix lactose operon repressor | |||
BNMOMFGJ_00788 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
BNMOMFGJ_00790 | 6.9e-134 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
BNMOMFGJ_00791 | 1.4e-94 | queF | 1.7.1.13 | S | Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily | |
BNMOMFGJ_00792 | 1.6e-134 | 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 | |
BNMOMFGJ_00793 | 1.4e-80 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
BNMOMFGJ_00794 | 3.6e-69 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
BNMOMFGJ_00797 | 9.8e-41 | traD | S | COG0433 Predicted ATPase | ||
BNMOMFGJ_00798 | 2.8e-108 | G | Belongs to the phosphoglycerate mutase family | |||
BNMOMFGJ_00799 | 1.1e-107 | G | Belongs to the phosphoglycerate mutase family | |||
BNMOMFGJ_00800 | 2.2e-108 | pgm | G | Belongs to the phosphoglycerate mutase family | ||
BNMOMFGJ_00801 | 3.9e-15 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
BNMOMFGJ_00802 | 3.6e-93 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
BNMOMFGJ_00803 | 5.8e-61 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
BNMOMFGJ_00804 | 3.6e-202 | 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 | |
BNMOMFGJ_00806 | 5.3e-80 | S | dextransucrase activity | |||
BNMOMFGJ_00807 | 2.4e-225 | GM | domain, Protein | |||
BNMOMFGJ_00808 | 1.4e-86 | ilvE | 2.6.1.42 | E | Aminotransferase | |
BNMOMFGJ_00809 | 2.3e-265 | 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 | |
BNMOMFGJ_00810 | 6.7e-51 | yebC | M | Membrane | ||
BNMOMFGJ_00811 | 2.3e-304 | KT | response to antibiotic | |||
BNMOMFGJ_00812 | 1.3e-154 | pstA | P | phosphate transport system permease | ||
BNMOMFGJ_00813 | 4e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
BNMOMFGJ_00814 | 1e-240 | 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 | ||
BNMOMFGJ_00815 | 1.1e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
BNMOMFGJ_00816 | 2.4e-90 | 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 | ||
BNMOMFGJ_00817 | 3.8e-159 | cvfB | S | Protein conserved in bacteria | ||
BNMOMFGJ_00818 | 3.7e-34 | yozE | S | Belongs to the UPF0346 family | ||
BNMOMFGJ_00819 | 4.4e-112 | 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) | |
BNMOMFGJ_00820 | 7.7e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
BNMOMFGJ_00821 | 2.1e-126 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
BNMOMFGJ_00822 | 0.0 | mprF | 2.3.2.3 | J | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
BNMOMFGJ_00823 | 2.3e-150 | cobQ | S | glutamine amidotransferase | ||
BNMOMFGJ_00824 | 8.2e-137 | IQ | Acetoin reductase | |||
BNMOMFGJ_00826 | 1.3e-46 | azlD | S | branched-chain amino acid | ||
BNMOMFGJ_00827 | 3e-114 | azlC | E | AzlC protein | ||
BNMOMFGJ_00828 | 1.3e-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 | |
BNMOMFGJ_00829 | 2e-71 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
BNMOMFGJ_00830 | 8.1e-38 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
BNMOMFGJ_00831 | 1.2e-247 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
BNMOMFGJ_00832 | 1.3e-13 | |||||
BNMOMFGJ_00833 | 5.3e-68 | ywiB | S | Domain of unknown function (DUF1934) | ||
BNMOMFGJ_00834 | 1.1e-208 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
BNMOMFGJ_00835 | 3.5e-140 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
BNMOMFGJ_00836 | 7.4e-211 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
BNMOMFGJ_00837 | 6.8e-245 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
BNMOMFGJ_00838 | 5.9e-55 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
BNMOMFGJ_00840 | 1.2e-208 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BNMOMFGJ_00841 | 4.3e-82 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BNMOMFGJ_00842 | 7.5e-225 | 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 | ||
BNMOMFGJ_00843 | 9.7e-22 | |||||
BNMOMFGJ_00844 | 9.9e-91 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
BNMOMFGJ_00845 | 1.5e-45 | 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 | |
BNMOMFGJ_00846 | 3.5e-205 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
BNMOMFGJ_00847 | 8.2e-60 | XK27_04120 | S | Putative amino acid metabolism | ||
BNMOMFGJ_00848 | 7.3e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
BNMOMFGJ_00849 | 1.7e-24 | 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 | ||
BNMOMFGJ_00850 | 2.9e-99 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
BNMOMFGJ_00851 | 7.8e-190 | femA | 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
BNMOMFGJ_00852 | 5.4e-147 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNMOMFGJ_00853 | 7.4e-228 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BNMOMFGJ_00854 | 2.5e-222 | capA | M | Bacterial capsule synthesis protein | ||
BNMOMFGJ_00855 | 6.1e-39 | gcvR | T | UPF0237 protein | ||
BNMOMFGJ_00856 | 2.8e-174 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
BNMOMFGJ_00857 | 4.4e-45 | rpmE2 | J | 50S ribosomal protein L31 | ||
BNMOMFGJ_00858 | 9.2e-175 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
BNMOMFGJ_00859 | 2.3e-139 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
BNMOMFGJ_00860 | 6.7e-116 | ylfI | S | tigr01906 | ||
BNMOMFGJ_00861 | 2.3e-136 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
BNMOMFGJ_00862 | 1.9e-222 | XK27_05470 | E | Methionine synthase | ||
BNMOMFGJ_00863 | 3.8e-156 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
BNMOMFGJ_00864 | 5.8e-55 | S | TM2 domain | |||
BNMOMFGJ_00865 | 5.5e-44 | |||||
BNMOMFGJ_00867 | 5.8e-95 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
BNMOMFGJ_00868 | 3.6e-76 | 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 | ||
BNMOMFGJ_00869 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
BNMOMFGJ_00870 | 1.8e-105 | 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 | |
BNMOMFGJ_00871 | 1.9e-75 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
BNMOMFGJ_00872 | 6e-126 | treR | K | trehalose operon | ||
BNMOMFGJ_00873 | 4.2e-84 | S | von Willebrand factor (vWF) type A domain | |||
BNMOMFGJ_00874 | 6.4e-130 | S | Appr-1'-p processing enzyme | |||
BNMOMFGJ_00875 | 6.5e-232 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
BNMOMFGJ_00876 | 8.1e-50 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
BNMOMFGJ_00877 | 1.7e-17 | yjdB | S | Domain of unknown function (DUF4767) | ||
BNMOMFGJ_00878 | 3.9e-198 | XK27_00915 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
BNMOMFGJ_00880 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
BNMOMFGJ_00881 | 1.5e-36 | ylqC | L | Belongs to the UPF0109 family | ||
BNMOMFGJ_00882 | 9.7e-236 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
BNMOMFGJ_00884 | 8.8e-51 | XK27_01300 | P | Protein conserved in bacteria | ||
BNMOMFGJ_00885 | 5.5e-206 | trkA | P | Potassium transporter peripheral membrane component | ||
BNMOMFGJ_00886 | 2.6e-33 | |||||
BNMOMFGJ_00887 | 1.7e-38 | DJ | Psort location Cytoplasmic, score | |||
BNMOMFGJ_00888 | 8.7e-142 | bmgA | U | Relaxase mobilization nuclease domain protein | ||
BNMOMFGJ_00889 | 4.7e-76 | |||||
BNMOMFGJ_00890 | 1.8e-128 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
BNMOMFGJ_00891 | 1.4e-181 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
BNMOMFGJ_00892 | 2.1e-83 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
BNMOMFGJ_00893 | 1.5e-81 | mreD | M | rod shape-determining protein MreD | ||
BNMOMFGJ_00894 | 9.1e-234 | sufD | O | assembly protein SufD | ||
BNMOMFGJ_00895 | 1.7e-137 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
BNMOMFGJ_00896 | 1.5e-132 | ecsA_2 | V | abc transporter atp-binding protein | ||
BNMOMFGJ_00897 | 7.4e-178 | smc | D | Required for chromosome condensation and partitioning | ||
BNMOMFGJ_00898 | 1.6e-22 | S | Protein of unknown function (DUF3278) | |||
BNMOMFGJ_00899 | 7.3e-94 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
BNMOMFGJ_00900 | 8.7e-128 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BNMOMFGJ_00901 | 2e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
BNMOMFGJ_00902 | 4.5e-196 | yceA | S | Belongs to the UPF0176 family | ||
BNMOMFGJ_00903 | 1.6e-28 | XK27_00085 | K | Transcriptional | ||
BNMOMFGJ_00904 | 7.4e-22 | |||||
BNMOMFGJ_00905 | 1e-85 | 3.4.21.110 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
BNMOMFGJ_00906 | 2.1e-174 | S | oxidoreductase | |||
BNMOMFGJ_00907 | 6.2e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
BNMOMFGJ_00908 | 5.1e-86 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
BNMOMFGJ_00909 | 9.7e-46 | clpE | O | Belongs to the ClpA ClpB family | ||
BNMOMFGJ_00910 | 4.1e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
BNMOMFGJ_00911 | 1.3e-139 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
BNMOMFGJ_00912 | 3e-209 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | adenylyltransferase | |
BNMOMFGJ_00913 | 5.4e-124 | L | Helix-turn-helix domain | |||
BNMOMFGJ_00914 | 2.2e-146 | L | Integrase core domain protein | |||
BNMOMFGJ_00915 | 1.6e-21 | 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 | |
BNMOMFGJ_00916 | 3.2e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
BNMOMFGJ_00917 | 2.2e-151 | 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 | |
BNMOMFGJ_00918 | 1e-104 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
BNMOMFGJ_00919 | 1e-68 | S | cog cog4699 | |||
BNMOMFGJ_00920 | 7.9e-163 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BNMOMFGJ_00922 | 2.5e-204 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
BNMOMFGJ_00925 | 4.8e-16 | S | Protein of unknown function (DUF2969) | |||
BNMOMFGJ_00926 | 1.1e-22 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
BNMOMFGJ_00927 | 3.5e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
BNMOMFGJ_00928 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
BNMOMFGJ_00929 | 3.9e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
BNMOMFGJ_00930 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
BNMOMFGJ_00931 | 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 | ||
BNMOMFGJ_00932 | 1.5e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
BNMOMFGJ_00934 | 6.1e-68 | 2.7.13.3 | T | GHKL domain | ||
BNMOMFGJ_00935 | 6.6e-66 | ssb_2 | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
BNMOMFGJ_00936 | 5.1e-90 | 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) | |
BNMOMFGJ_00939 | 5.2e-127 | S | Tetratricopeptide repeat protein | |||
BNMOMFGJ_00940 | 7.8e-08 | uvrX | 2.7.7.7 | L | impB/mucB/samB family | |
BNMOMFGJ_00941 | 8.7e-254 | cycA | E | permease | ||
BNMOMFGJ_00942 | 2.2e-142 | plsC | 2.3.1.51 | I | Acyltransferase | |
BNMOMFGJ_00943 | 3.1e-146 | nodB3 | G | Polysaccharide deacetylase | ||
BNMOMFGJ_00944 | 5e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
BNMOMFGJ_00945 | 7.7e-155 | pyrP | F | uracil Permease | ||
BNMOMFGJ_00946 | 1.5e-135 | stp | 3.1.3.16 | T | phosphatase | |
BNMOMFGJ_00947 | 1.8e-152 | XK27_05675 | S | Esterase | ||
BNMOMFGJ_00948 | 3.9e-161 | XK27_05670 | S | Putative esterase | ||
BNMOMFGJ_00949 | 1.3e-54 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
BNMOMFGJ_00950 | 6.6e-78 | ureE | O | enzyme active site formation | ||
BNMOMFGJ_00951 | 3.9e-181 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
BNMOMFGJ_00952 | 2e-28 | zmpB | M | signal peptide protein, YSIRK family | ||
BNMOMFGJ_00953 | 7.7e-164 | L | High confidence in function and specificity | |||
BNMOMFGJ_00954 | 2.2e-42 | S | Fibronectin-binding repeat | |||
BNMOMFGJ_00955 | 9.1e-127 | K | response regulator | |||
BNMOMFGJ_00956 | 1.6e-175 | saeS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
BNMOMFGJ_00957 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BNMOMFGJ_00958 | 3.2e-29 | yyzM | S | Protein conserved in bacteria | ||
BNMOMFGJ_00959 | 5.2e-72 | copY | K | negative regulation of transcription, DNA-templated | ||
BNMOMFGJ_00960 | 4.9e-146 | XK27_00115 | 2.3.1.128 | K | Acetyltransferase GNAT family | |
BNMOMFGJ_00961 | 8.4e-163 | ybbR | S | Protein conserved in bacteria | ||
BNMOMFGJ_00962 | 6.2e-123 | 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 | |
BNMOMFGJ_00963 | 2.2e-109 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
BNMOMFGJ_00964 | 2.7e-269 | T | PhoQ Sensor | |||
BNMOMFGJ_00965 | 3e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
BNMOMFGJ_00966 | 2.4e-90 | cvpA | S | toxin biosynthetic process | ||
BNMOMFGJ_00967 | 9.3e-15 | 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 | ||
BNMOMFGJ_00968 | 1.7e-154 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BNMOMFGJ_00970 | 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 | ||
BNMOMFGJ_00971 | 3.2e-76 | S | Psort location Cytoplasmic, score 8.96 | |||
BNMOMFGJ_00972 | 1.5e-167 | L | Psort location Cytoplasmic, score 8.96 | |||
BNMOMFGJ_00973 | 3.3e-42 | XCC2107 | L | SPTR Transposase | ||
BNMOMFGJ_00974 | 3.9e-229 | malX | G | ABC transporter | ||
BNMOMFGJ_00975 | 1.2e-112 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BNMOMFGJ_00976 | 1.8e-100 | S | CAAX amino terminal protease family protein | |||
BNMOMFGJ_00978 | 4.9e-81 | XK27_05680 | 6.3.2.2, 6.3.2.4 | M | carbamoylphosphate synthase large subunit | |
BNMOMFGJ_00979 | 6e-178 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
BNMOMFGJ_00980 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
BNMOMFGJ_00981 | 3.3e-138 | M | LysM domain | |||
BNMOMFGJ_00982 | 8.4e-23 | |||||
BNMOMFGJ_00983 | 4.6e-49 | K | COG3279 Response regulator of the LytR AlgR family | |||
BNMOMFGJ_00984 | 2.2e-30 | S | Protein of unknown function (DUF3021) | |||
BNMOMFGJ_00985 | 3.5e-118 | mta | K | Transcriptional | ||
BNMOMFGJ_00987 | 3e-229 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BNMOMFGJ_00988 | 9.7e-22 | clpE | O | Belongs to the ClpA ClpB family | ||
BNMOMFGJ_00989 | 3.7e-182 | 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 | |
BNMOMFGJ_00990 | 1e-34 | ykuJ | S | protein conserved in bacteria | ||
BNMOMFGJ_00991 | 1.8e-90 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
BNMOMFGJ_00992 | 5.9e-216 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
BNMOMFGJ_00993 | 9.6e-89 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
BNMOMFGJ_00994 | 2.3e-131 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
BNMOMFGJ_00995 | 6.4e-246 | 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 | ||
BNMOMFGJ_00996 | 1.5e-203 | 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 | ||
BNMOMFGJ_00997 | 3.7e-58 | yaaA | S | S4 domain protein YaaA | ||
BNMOMFGJ_00998 | 2.7e-67 | 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) | ||
BNMOMFGJ_00999 | 1.7e-57 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BNMOMFGJ_01000 | 9.5e-22 | divIC | D | Septum formation initiator | ||
BNMOMFGJ_01002 | 9.3e-234 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
BNMOMFGJ_01003 | 7.2e-26 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
BNMOMFGJ_01004 | 1.3e-232 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BNMOMFGJ_01005 | 1.3e-246 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
BNMOMFGJ_01006 | 1.4e-132 | L | Transposase | |||
BNMOMFGJ_01007 | 8.7e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
BNMOMFGJ_01008 | 1.5e-86 | 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) | |
BNMOMFGJ_01009 | 1.8e-60 | |||||
BNMOMFGJ_01010 | 1.6e-75 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
BNMOMFGJ_01011 | 6.2e-202 | rny | D | Endoribonuclease that initiates mRNA decay | ||
BNMOMFGJ_01012 | 6.4e-188 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
BNMOMFGJ_01013 | 7.6e-67 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
BNMOMFGJ_01014 | 5.1e-306 | ybiT | S | abc transporter atp-binding protein | ||
BNMOMFGJ_01015 | 2.2e-51 | yvjA | S | membrane | ||
BNMOMFGJ_01016 | 3.6e-68 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
BNMOMFGJ_01017 | 3.3e-144 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
BNMOMFGJ_01018 | 9.7e-89 | glcR | K | transcriptional regulator (DeoR family) | ||
BNMOMFGJ_01019 | 0.0 | S | dextransucrase activity | |||
BNMOMFGJ_01022 | 2.2e-87 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
BNMOMFGJ_01023 | 3.1e-69 | argR | K | Regulates arginine biosynthesis genes | ||
BNMOMFGJ_01024 | 8.2e-66 | silP | 1.9.3.1, 3.6.3.54 | S | cog cog4633 | |
BNMOMFGJ_01025 | 7.1e-72 | K | transcriptional | |||
BNMOMFGJ_01026 | 2.7e-234 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
BNMOMFGJ_01028 | 3.6e-78 | dprA | LU | DNA protecting protein DprA | ||
BNMOMFGJ_01029 | 3.1e-52 | |||||
BNMOMFGJ_01030 | 1.5e-70 | |||||
BNMOMFGJ_01031 | 1.1e-23 | L | Transposase and inactivated derivatives IS30 family | |||
BNMOMFGJ_01032 | 3.2e-144 | 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( ) | ||
BNMOMFGJ_01033 | 1.8e-93 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
BNMOMFGJ_01034 | 2.8e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
BNMOMFGJ_01036 | 9.7e-233 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
BNMOMFGJ_01037 | 3.2e-84 | lytC | 3.4.17.14, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
BNMOMFGJ_01038 | 9.5e-175 | 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) | |
BNMOMFGJ_01039 | 3.8e-218 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
BNMOMFGJ_01040 | 7.2e-121 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
BNMOMFGJ_01043 | 3.3e-57 | S | Protein of unknown function (Porph_ging) | |||
BNMOMFGJ_01045 | 5.3e-27 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
BNMOMFGJ_01046 | 2.3e-292 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
BNMOMFGJ_01047 | 3.3e-10 | 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 | |
BNMOMFGJ_01048 | 7e-132 | 2.7.13.3, 2.7.7.7, 5.4.99.21 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
BNMOMFGJ_01049 | 5.1e-156 | 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 | |
BNMOMFGJ_01050 | 1.2e-55 | I | Alpha/beta hydrolase family | |||
BNMOMFGJ_01052 | 1.1e-184 | nss | M | transferase activity, transferring glycosyl groups | ||
BNMOMFGJ_01053 | 3.6e-16 | S | Accessory secretory protein Sec, Asp5 | |||
BNMOMFGJ_01054 | 2.6e-17 | S | Accessory secretory protein Sec Asp4 | |||
BNMOMFGJ_01055 | 4.1e-28 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
BNMOMFGJ_01056 | 3e-93 | comEC | S | Competence protein ComEC | ||
BNMOMFGJ_01057 | 7.9e-73 | cbiQ | P | cobalt transport | ||
BNMOMFGJ_01058 | 1.5e-118 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
BNMOMFGJ_01059 | 6e-83 | P | COG0168 Trk-type K transport systems, membrane components | |||
BNMOMFGJ_01060 | 1.2e-174 | S | hydrolase | |||
BNMOMFGJ_01062 | 1.3e-159 | 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 | |
BNMOMFGJ_01063 | 9.2e-144 | 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 | |
BNMOMFGJ_01064 | 2.1e-45 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
BNMOMFGJ_01065 | 1.9e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
BNMOMFGJ_01066 | 2.6e-107 | V | permease protein | |||
BNMOMFGJ_01067 | 1.7e-196 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
BNMOMFGJ_01070 | 3.6e-37 | |||||
BNMOMFGJ_01071 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolase 101 beta sandwich domain | |
BNMOMFGJ_01072 | 1.1e-93 | 3.2.1.97 | GH101 | G | Glycosyl hydrolase 101 beta sandwich domain | |
BNMOMFGJ_01073 | 4e-121 | yoaK | S | Protein of unknown function (DUF1275) | ||
BNMOMFGJ_01076 | 9.1e-28 | efeU_1 | P | Iron permease FTR1 family | ||
BNMOMFGJ_01077 | 7.5e-151 | efeU_1 | P | Iron permease FTR1 family | ||
BNMOMFGJ_01078 | 7.9e-99 | tpd | P | Fe2+ transport protein | ||
BNMOMFGJ_01079 | 3.1e-116 | S | Predicted membrane protein (DUF2318) | |||
BNMOMFGJ_01080 | 5.7e-112 | K | Acetyltransferase (GNAT) family | |||
BNMOMFGJ_01081 | 7.1e-181 | lmrA2 | V | abc transporter atp-binding protein | ||
BNMOMFGJ_01082 | 1.7e-268 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
BNMOMFGJ_01083 | 1.1e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
BNMOMFGJ_01084 | 2.5e-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 | ||
BNMOMFGJ_01085 | 1.9e-46 | ylbG | S | UPF0298 protein | ||
BNMOMFGJ_01086 | 1.7e-73 | ylbF | S | Belongs to the UPF0342 family | ||
BNMOMFGJ_01087 | 3.1e-81 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
BNMOMFGJ_01088 | 5.8e-51 | |||||
BNMOMFGJ_01089 | 1e-44 | |||||
BNMOMFGJ_01090 | 1.1e-297 | bcsA | 2.4.1.12 | GT2 | M | COG1215 Glycosyltransferases, probably involved in cell wall biogenesis |
BNMOMFGJ_01091 | 2.4e-150 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BNMOMFGJ_01092 | 4.8e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
BNMOMFGJ_01093 | 2.9e-125 | trpF | 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
BNMOMFGJ_01094 | 2.8e-114 | P | ATPases associated with a variety of cellular activities | |||
BNMOMFGJ_01095 | 8.6e-165 | norN | V | Mate efflux family protein | ||
BNMOMFGJ_01096 | 1.4e-57 | asp | S | cog cog1302 | ||
BNMOMFGJ_01097 | 2.8e-120 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination | |
BNMOMFGJ_01098 | 0.0 | secA2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
BNMOMFGJ_01099 | 5.6e-275 | 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 | |
BNMOMFGJ_01100 | 1.5e-225 | 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 | ||
BNMOMFGJ_01101 | 6.8e-187 | yeeE | S | Sulphur transport | ||
BNMOMFGJ_01102 | 8.3e-37 | yeeD | O | sulfur carrier activity | ||
BNMOMFGJ_01103 | 1.2e-54 | yabA | L | Involved in initiation control of chromosome replication | ||
BNMOMFGJ_01104 | 3.1e-114 | yaaT | S | stage 0 sporulation protein | ||
BNMOMFGJ_01105 | 2.4e-192 | 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 | ||
BNMOMFGJ_01106 | 5.1e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
BNMOMFGJ_01107 | 1.5e-161 | yxeN | P | ABC transporter (Permease | ||
BNMOMFGJ_01108 | 5.6e-113 | L | Transposase | |||
BNMOMFGJ_01109 | 1e-118 | L | HTH-like domain | |||
BNMOMFGJ_01110 | 1.5e-152 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
BNMOMFGJ_01112 | 2e-09 | |||||
BNMOMFGJ_01114 | 2.2e-90 | rodA | D | Belongs to the SEDS family | ||
BNMOMFGJ_01116 | 5.2e-223 | ytfP | S | Flavoprotein | ||
BNMOMFGJ_01117 | 8.6e-204 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
BNMOMFGJ_01118 | 7e-59 | 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 | |
BNMOMFGJ_01119 | 2.4e-47 | nusA | K | Participates in both transcription termination and antitermination | ||
BNMOMFGJ_01120 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
BNMOMFGJ_01121 | 8e-42 | ylxQ | J | ribosomal protein | ||
BNMOMFGJ_01122 | 4.3e-93 | macB_2 | V | FtsX-like permease family | ||
BNMOMFGJ_01123 | 5.5e-118 | 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 | |
BNMOMFGJ_01124 | 1.3e-179 | 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 | |
BNMOMFGJ_01125 | 2.3e-268 | 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 | ||
BNMOMFGJ_01127 | 6.6e-81 | smpB | O | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
BNMOMFGJ_01128 | 3.3e-30 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BNMOMFGJ_01129 | 1.4e-170 | 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 | |
BNMOMFGJ_01130 | 2e-97 | mip | S | hydroperoxide reductase activity | ||
BNMOMFGJ_01131 | 9.8e-73 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
BNMOMFGJ_01132 | 2.6e-194 | 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 | |
BNMOMFGJ_01133 | 1.7e-268 | mdlB | V | abc transporter atp-binding protein | ||
BNMOMFGJ_01134 | 2.8e-18 | artJ_1 | ET | Belongs to the bacterial solute-binding protein 3 family | ||
BNMOMFGJ_01135 | 1.4e-81 | yecS | P | ABC transporter (Permease | ||
BNMOMFGJ_01137 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
BNMOMFGJ_01138 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
BNMOMFGJ_01139 | 1.6e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
BNMOMFGJ_01140 | 1.7e-99 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
BNMOMFGJ_01141 | 2.1e-185 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
BNMOMFGJ_01142 | 7.2e-203 | cps2J | S | Polysaccharide biosynthesis protein | ||
BNMOMFGJ_01143 | 4.8e-286 | menD | 2.2.1.9 | H | Thiamine pyrophosphate enzyme, N-terminal TPP binding domain | |
BNMOMFGJ_01144 | 2.6e-123 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BNMOMFGJ_01145 | 2.9e-173 | S | slime layer polysaccharide biosynthetic process | |||
BNMOMFGJ_01146 | 8.8e-51 | |||||
BNMOMFGJ_01147 | 3.4e-76 | GT2 | M | Glycosyl transferase, group 2 family protein | ||
BNMOMFGJ_01148 | 3.2e-185 | rgpAc | GT4 | M | Domain of unknown function (DUF1972) | |
BNMOMFGJ_01149 | 1.1e-56 | L | Transposase | |||
BNMOMFGJ_01150 | 5.5e-158 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
BNMOMFGJ_01151 | 2e-264 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
BNMOMFGJ_01152 | 5.4e-63 | L | Integrase core domain protein | |||
BNMOMFGJ_01153 | 3.6e-12 | L | Psort location Cytoplasmic, score 8.96 | |||
BNMOMFGJ_01154 | 1.8e-119 | XK27_08635 | S | UPF0210 protein | ||
BNMOMFGJ_01155 | 4.3e-132 | ais | G | Phosphoglycerate mutase | ||
BNMOMFGJ_01156 | 6.7e-204 | zmpB | M | signal peptide protein, YSIRK family | ||
BNMOMFGJ_01157 | 5.9e-202 | 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) | |
BNMOMFGJ_01158 | 1.5e-133 | yxkH | G | deacetylase | ||
BNMOMFGJ_01159 | 1.2e-106 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
BNMOMFGJ_01160 | 1.2e-213 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
BNMOMFGJ_01161 | 5.7e-74 | 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 | ||
BNMOMFGJ_01162 | 1.3e-94 | 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 | ||
BNMOMFGJ_01163 | 1.1e-80 | 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 | ||
BNMOMFGJ_01164 | 8.5e-193 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
BNMOMFGJ_01165 | 2.1e-191 | yjcE | P | NhaP-type Na H and K H antiporters | ||
BNMOMFGJ_01166 | 4e-22 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
BNMOMFGJ_01167 | 2.6e-156 | L | Replication initiation factor | |||
BNMOMFGJ_01168 | 1.9e-18 | S | Domain of unknown function (DUF3173) | |||
BNMOMFGJ_01169 | 2.9e-215 | int | L | Belongs to the 'phage' integrase family | ||
BNMOMFGJ_01171 | 2.4e-234 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
BNMOMFGJ_01172 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
BNMOMFGJ_01173 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
BNMOMFGJ_01174 | 1.8e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
BNMOMFGJ_01175 | 3.2e-44 | yrzB | S | Belongs to the UPF0473 family | ||
BNMOMFGJ_01176 | 1.5e-292 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
BNMOMFGJ_01177 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
BNMOMFGJ_01178 | 1.7e-13 | |||||
BNMOMFGJ_01179 | 2.4e-89 | XK27_10930 | K | acetyltransferase | ||
BNMOMFGJ_01180 | 8.2e-116 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
BNMOMFGJ_01181 | 3.9e-27 | yaaA | S | Belongs to the UPF0246 family | ||
BNMOMFGJ_01183 | 2.9e-31 | yozG | K | Transcriptional regulator | ||
BNMOMFGJ_01185 | 2e-94 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
BNMOMFGJ_01186 | 5.1e-22 | K | Transcriptional | |||
BNMOMFGJ_01187 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
BNMOMFGJ_01188 | 1.2e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
BNMOMFGJ_01189 | 1.2e-111 | 3.5.1.28 | M | domain protein | ||
BNMOMFGJ_01190 | 8.9e-98 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BNMOMFGJ_01191 | 1.3e-108 | ykuT | M | mechanosensitive ion channel | ||
BNMOMFGJ_01192 | 1.9e-86 | sigH | K | DNA-templated transcription, initiation | ||
BNMOMFGJ_01194 | 2.2e-151 | degV | S | DegV family | ||
BNMOMFGJ_01195 | 6e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
BNMOMFGJ_01196 | 2.8e-88 | 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 | ||
BNMOMFGJ_01197 | 6.1e-94 | cvpA | S | toxin biosynthetic process | ||
BNMOMFGJ_01198 | 9.3e-15 | 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 | ||
BNMOMFGJ_01199 | 1.2e-207 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
BNMOMFGJ_01200 | 2.6e-138 | yitS | S | EDD domain protein, DegV family | ||
BNMOMFGJ_01201 | 2.3e-53 | S | Bacterial protein of unknown function (DUF961) | |||
BNMOMFGJ_01202 | 1e-63 | S | Bacterial protein of unknown function (DUF961) | |||
BNMOMFGJ_01203 | 3.7e-265 | D | Domain of unknown function DUF87 | |||
BNMOMFGJ_01204 | 1.6e-232 | K | Replication initiation factor | |||
BNMOMFGJ_01205 | 1.9e-30 | S | Psort location CytoplasmicMembrane, score | |||
BNMOMFGJ_01206 | 7.5e-91 | S | Antirestriction protein (ArdA) | |||
BNMOMFGJ_01207 | 3.8e-90 | S | TcpE family | |||
BNMOMFGJ_01208 | 0.0 | S | AAA-like domain | |||
BNMOMFGJ_01209 | 0.0 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
BNMOMFGJ_01210 | 2.2e-190 | yddH | M | NlpC p60 family protein | ||
BNMOMFGJ_01211 | 6.7e-113 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
BNMOMFGJ_01212 | 2.3e-90 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
BNMOMFGJ_01214 | 1.3e-114 | ytxK | 2.1.1.72 | L | DNA methylase | |
BNMOMFGJ_01215 | 1.3e-16 | |||||
BNMOMFGJ_01216 | 1.6e-26 | XK27_00515 | D | Cell surface antigen C-terminus | ||
BNMOMFGJ_01217 | 5.7e-132 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
BNMOMFGJ_01218 | 3.2e-83 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
BNMOMFGJ_01219 | 1.4e-157 | T | PhoQ Sensor | |||
BNMOMFGJ_01220 | 4.9e-103 | thiJ-2 | 3.5.1.124 | S | DJ-1/PfpI family | |
BNMOMFGJ_01221 | 4.9e-128 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
BNMOMFGJ_01222 | 9.8e-95 | cylA | V | abc transporter atp-binding protein | ||
BNMOMFGJ_01223 | 5.1e-132 | cylB | V | ABC-2 type transporter | ||
BNMOMFGJ_01224 | 8.6e-179 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
BNMOMFGJ_01225 | 1.3e-64 | gtrA | S | GtrA-like protein | ||
BNMOMFGJ_01226 | 2.2e-157 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
BNMOMFGJ_01227 | 3.7e-143 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
BNMOMFGJ_01228 | 7.6e-91 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
BNMOMFGJ_01229 | 7.5e-218 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
BNMOMFGJ_01230 | 2.6e-76 | yegQ | O | Peptidase U32 | ||
BNMOMFGJ_01231 | 1.1e-87 | bioY | S | biotin synthase | ||
BNMOMFGJ_01232 | 6.9e-53 | S | membrane | |||
BNMOMFGJ_01233 | 8.2e-69 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
BNMOMFGJ_01234 | 9.7e-36 | XK27_09805 | S | MORN repeat protein | ||
BNMOMFGJ_01235 | 1.4e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
BNMOMFGJ_01237 | 2.7e-69 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
BNMOMFGJ_01238 | 1e-84 | yxjI | S | LURP-one-related | ||
BNMOMFGJ_01239 | 1.6e-84 | 2.4.1.83 | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
BNMOMFGJ_01240 | 2.6e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
BNMOMFGJ_01242 | 9.7e-215 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
BNMOMFGJ_01243 | 2e-123 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
BNMOMFGJ_01244 | 1e-176 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
BNMOMFGJ_01245 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
BNMOMFGJ_01246 | 2.7e-311 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
BNMOMFGJ_01247 | 1.1e-275 | amiC | P | ABC transporter (Permease | ||
BNMOMFGJ_01248 | 3.8e-165 | amiD | P | ABC transporter (Permease | ||
BNMOMFGJ_01249 | 5.4e-203 | oppD | P | Belongs to the ABC transporter superfamily | ||
BNMOMFGJ_01250 | 9.5e-172 | oppF | P | Belongs to the ABC transporter superfamily | ||
BNMOMFGJ_01251 | 9.1e-57 | V | Psort location CytoplasmicMembrane, score | |||
BNMOMFGJ_01252 | 4.2e-175 | coiA | 3.6.4.12 | S | Competence protein | |
BNMOMFGJ_01253 | 5.5e-124 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
BNMOMFGJ_01254 | 7e-104 | sufB | O | assembly protein SufB | ||
BNMOMFGJ_01255 | 2.7e-26 | |||||
BNMOMFGJ_01256 | 2.2e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
BNMOMFGJ_01257 | 2.9e-66 | dltB | M | Membrane protein involved in D-alanine export | ||
BNMOMFGJ_01258 | 9e-10 | S | Protein of unknown function (DUF1146) | |||
BNMOMFGJ_01259 | 1.3e-170 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
BNMOMFGJ_01260 | 1.1e-84 | dnaB | L | Replication initiation and membrane attachment | ||
BNMOMFGJ_01261 | 5.6e-62 | yvoA_1 | K | Transcriptional | ||
BNMOMFGJ_01262 | 2e-118 | skfE | V | abc transporter atp-binding protein | ||
BNMOMFGJ_01263 | 3.2e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
BNMOMFGJ_01264 | 4.9e-93 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
BNMOMFGJ_01265 | 5.6e-222 | mutY | L | A G-specific adenine glycosylase | ||
BNMOMFGJ_01266 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
BNMOMFGJ_01267 | 6.3e-79 | comFC | S | Competence protein | ||
BNMOMFGJ_01269 | 9e-167 | fhuR | K | transcriptional regulator (lysR family) | ||
BNMOMFGJ_01270 | 9.7e-65 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
BNMOMFGJ_01271 | 5.1e-136 | 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 | ||
BNMOMFGJ_01272 | 6.6e-204 | L | Transposase | |||
BNMOMFGJ_01273 | 2.8e-188 | mvaS | 2.3.3.10 | I | synthase | |
BNMOMFGJ_01274 | 6.2e-169 | manL | 2.7.1.191 | G | pts system | |
BNMOMFGJ_01275 | 6.1e-271 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
BNMOMFGJ_01276 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
BNMOMFGJ_01277 | 4e-146 | |||||
BNMOMFGJ_01278 | 3.5e-276 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
BNMOMFGJ_01279 | 1.2e-211 | 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 | |
BNMOMFGJ_01280 | 7.8e-174 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
BNMOMFGJ_01281 | 2.9e-185 | 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 | |
BNMOMFGJ_01282 | 1.5e-91 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
BNMOMFGJ_01283 | 1.7e-129 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BNMOMFGJ_01284 | 1.7e-61 | yqhY | S | protein conserved in bacteria | ||
BNMOMFGJ_01285 | 1.2e-97 | 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 | ||
BNMOMFGJ_01297 | 2.6e-10 | |||||
BNMOMFGJ_01300 | 1.9e-07 | |||||
BNMOMFGJ_01301 | 5.7e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
BNMOMFGJ_01302 | 1.2e-12 | ard | S | Antirestriction protein (ArdA) | ||
BNMOMFGJ_01303 | 1e-93 | K | helix_turn _helix lactose operon repressor | |||
BNMOMFGJ_01304 | 7.4e-42 | gst | O | Glutathione S-transferase | ||
BNMOMFGJ_01305 | 2.6e-177 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
BNMOMFGJ_01306 | 2.8e-111 | M | Pilin isopeptide linkage domain protein | |||
BNMOMFGJ_01307 | 5.1e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BNMOMFGJ_01308 | 2.6e-09 | S | NTF2 fold immunity protein | |||
BNMOMFGJ_01309 | 1.2e-118 | liaI | S | membrane | ||
BNMOMFGJ_01310 | 5.8e-118 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
BNMOMFGJ_01311 | 1.1e-124 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
BNMOMFGJ_01313 | 2.7e-79 | 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 | |
BNMOMFGJ_01314 | 1.3e-60 | yhcC | S | radical SAM protein | ||
BNMOMFGJ_01315 | 2.2e-96 | ytqB | J | (SAM)-dependent | ||
BNMOMFGJ_01317 | 9e-148 | S | dextransucrase activity | |||
BNMOMFGJ_01318 | 5.4e-138 | glnA | 6.3.1.2 | E | glutamine synthetase | |
BNMOMFGJ_01319 | 3.1e-139 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
BNMOMFGJ_01320 | 1.1e-175 | 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 | |
BNMOMFGJ_01321 | 3.5e-112 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
BNMOMFGJ_01322 | 1.4e-98 | yqeG | S | hydrolase of the HAD superfamily | ||
BNMOMFGJ_01323 | 3e-82 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
BNMOMFGJ_01324 | 5.9e-225 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
BNMOMFGJ_01325 | 6.1e-213 | 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 | ||
BNMOMFGJ_01326 | 6.9e-101 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
BNMOMFGJ_01327 | 1.5e-29 | K | Helix-turn-helix domain | |||
BNMOMFGJ_01328 | 4.6e-20 | |||||
BNMOMFGJ_01330 | 1.8e-17 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
BNMOMFGJ_01331 | 8.9e-178 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
BNMOMFGJ_01332 | 1.2e-12 | XK27_11680 | ||||
BNMOMFGJ_01333 | 3.4e-26 | lanR | K | sequence-specific DNA binding | ||
BNMOMFGJ_01334 | 1.1e-101 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BNMOMFGJ_01335 | 4.6e-157 | aatB | ET | ABC transporter substrate-binding protein | ||
BNMOMFGJ_01336 | 4.4e-112 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
BNMOMFGJ_01337 | 1.4e-105 | artQ | P | ABC transporter (Permease | ||
BNMOMFGJ_01338 | 6.6e-59 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
BNMOMFGJ_01339 | 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 | |
BNMOMFGJ_01340 | 8.4e-165 | cpsY | K | Transcriptional regulator | ||
BNMOMFGJ_01341 | 9.3e-127 | mur1 | 3.4.17.14, 3.5.1.28 | NU | muramidase | |
BNMOMFGJ_01342 | 4.8e-169 | yeiH | S | Membrane | ||
BNMOMFGJ_01344 | 2.6e-09 | |||||
BNMOMFGJ_01345 | 8.5e-41 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18 | GH23 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
BNMOMFGJ_01346 | 6.2e-180 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
BNMOMFGJ_01347 | 6.9e-76 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
BNMOMFGJ_01348 | 2.5e-37 | fruA | 2.7.1.202 | G | phosphotransferase system | |
BNMOMFGJ_01349 | 9.1e-144 | supH | S | overlaps another CDS with the same product name | ||
BNMOMFGJ_01350 | 5.4e-135 | adcC | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
BNMOMFGJ_01351 | 2.6e-71 | adcR | K | transcriptional | ||
BNMOMFGJ_01352 | 1.3e-163 | L | Phage integrase, N-terminal SAM-like domain | |||
BNMOMFGJ_01353 | 2.2e-176 | L | Phage integrase family | |||
BNMOMFGJ_01354 | 3.5e-227 | xerC_1 | L | Belongs to the 'phage' integrase family | ||
BNMOMFGJ_01355 | 7.3e-93 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
BNMOMFGJ_01356 | 1.3e-303 | 3.2.1.55 | GH51 | G | arabinose metabolic process | |
BNMOMFGJ_01357 | 5.6e-294 | kup | P | Transport of potassium into the cell | ||
BNMOMFGJ_01358 | 1e-78 | yfiB1 | V | abc transporter atp-binding protein | ||
BNMOMFGJ_01359 | 3.9e-167 | 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 | ||
BNMOMFGJ_01360 | 2.2e-54 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
BNMOMFGJ_01361 | 3.7e-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 | |
BNMOMFGJ_01362 | 7.9e-123 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
BNMOMFGJ_01363 | 1.2e-32 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
BNMOMFGJ_01364 | 1.5e-34 | traD | S | COG0433 Predicted ATPase | ||
BNMOMFGJ_01365 | 2.5e-67 | S | Glutathione-dependent formaldehyde-activating | |||
BNMOMFGJ_01366 | 2.3e-156 | S | CHAP domain | |||
BNMOMFGJ_01367 | 1e-148 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
BNMOMFGJ_01368 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
BNMOMFGJ_01370 | 5.7e-141 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
BNMOMFGJ_01371 | 2.7e-91 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
BNMOMFGJ_01372 | 1.1e-49 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
BNMOMFGJ_01373 | 5.2e-101 | 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 | |
BNMOMFGJ_01374 | 3e-96 | P | VTC domain | |||
BNMOMFGJ_01375 | 1.4e-98 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
BNMOMFGJ_01376 | 2.4e-43 | nadK | 2.7.1.23 | H | 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 | |
BNMOMFGJ_01377 | 7.5e-25 | S | Protein of unknown function (DUF3114) | |||
BNMOMFGJ_01378 | 4.1e-29 | pspC | KT | PspC domain protein | ||
BNMOMFGJ_01379 | 1.9e-98 | yqfA | K | protein, Hemolysin III | ||
BNMOMFGJ_01380 | 1.2e-102 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
BNMOMFGJ_01381 | 2.9e-148 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
BNMOMFGJ_01382 | 8.6e-156 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
BNMOMFGJ_01383 | 2.7e-127 | cylB | V | ABC-2 type transporter | ||
BNMOMFGJ_01384 | 1.9e-75 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
BNMOMFGJ_01385 | 6.4e-84 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
BNMOMFGJ_01386 | 2.6e-58 | adk | 2.7.4.3 | F | topology modulation protein | |
BNMOMFGJ_01387 | 8e-202 | 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 | |
BNMOMFGJ_01388 | 3.9e-93 | L | Integrase core domain | |||
BNMOMFGJ_01389 | 1.7e-196 | L | Transposase | |||
BNMOMFGJ_01390 | 2.4e-78 | yhcA | V | abc transporter atp-binding protein | ||
BNMOMFGJ_01391 | 1.7e-145 | E | Alpha beta hydrolase | |||
BNMOMFGJ_01392 | 1.8e-190 | tcsA | S | membrane | ||
BNMOMFGJ_01393 | 1.6e-12 | V | Glucan-binding protein C | |||
BNMOMFGJ_01394 | 6.7e-254 | V | Glucan-binding protein C | |||
BNMOMFGJ_01395 | 1.5e-121 | 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 | |
BNMOMFGJ_01396 | 1.6e-232 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
BNMOMFGJ_01397 | 7.2e-95 | S | Protein of unknown function (DUF1697) | |||
BNMOMFGJ_01398 | 8.3e-148 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
BNMOMFGJ_01399 | 1.4e-21 | 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 | ||
BNMOMFGJ_01400 | 9.8e-10 | O | ADP-ribosylglycohydrolase | |||
BNMOMFGJ_01401 | 2e-45 | potD | P | spermidine putrescine ABC transporter | ||
BNMOMFGJ_01402 | 1.6e-144 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
BNMOMFGJ_01403 | 1.8e-71 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
BNMOMFGJ_01404 | 4.4e-158 | GK | ROK family | |||
BNMOMFGJ_01405 | 3e-209 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
BNMOMFGJ_01406 | 1e-104 | wecD | M | Acetyltransferase (GNAT) domain | ||
BNMOMFGJ_01407 | 1.2e-219 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BNMOMFGJ_01408 | 7.8e-72 | ogt | 2.1.1.63, 3.2.2.20 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
BNMOMFGJ_01409 | 2.7e-58 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
BNMOMFGJ_01411 | 3.5e-56 | lrgA | S | Effector of murein hydrolase LrgA | ||
BNMOMFGJ_01412 | 1.6e-115 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like proteins CidA and or CidB. The LrgAB and CidAB proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
BNMOMFGJ_01413 | 5.5e-98 | 3.1.3.18 | S | IA, variant 1 | ||
BNMOMFGJ_01414 | 1.8e-87 | dcuS | 2.7.13.3 | T | protein histidine kinase activity | |
BNMOMFGJ_01415 | 3.5e-36 | 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 | |
BNMOMFGJ_01416 | 3.9e-114 | S | VIT family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)