ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
NHEFJLLP_00001 | 6.8e-156 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
NHEFJLLP_00002 | 1.4e-192 | rliB | K | helix_turn_helix gluconate operon transcriptional repressor | ||
NHEFJLLP_00003 | 2.5e-311 | yknV | V | ABC transporter | ||
NHEFJLLP_00004 | 0.0 | mdlA2 | V | ABC transporter | ||
NHEFJLLP_00005 | 1.6e-154 | K | AraC-like ligand binding domain | |||
NHEFJLLP_00006 | 0.0 | 3.2.1.52 | GH20 | G | Glycosyl hydrolase family 20, catalytic domain | |
NHEFJLLP_00007 | 5.2e-181 | U | Binding-protein-dependent transport system inner membrane component | |||
NHEFJLLP_00008 | 3.3e-161 | lplC | U | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_00009 | 9.8e-280 | G | Domain of unknown function (DUF3502) | |||
NHEFJLLP_00010 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
NHEFJLLP_00011 | 4.1e-107 | ypcB | S | integral membrane protein | ||
NHEFJLLP_00012 | 0.0 | yesM | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_00013 | 6.3e-271 | yesN | K | helix_turn_helix, arabinose operon control protein | ||
NHEFJLLP_00014 | 5.2e-164 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
NHEFJLLP_00015 | 9.1e-217 | msmX | P | Belongs to the ABC transporter superfamily | ||
NHEFJLLP_00016 | 0.0 | ypdD | G | Glycosyl hydrolase family 92 | ||
NHEFJLLP_00017 | 1.8e-195 | rliB | K | Transcriptional regulator | ||
NHEFJLLP_00018 | 1.5e-252 | S | Metal-independent alpha-mannosidase (GH125) | |||
NHEFJLLP_00019 | 0.0 | mngB | 2.3.1.204, 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
NHEFJLLP_00020 | 3.9e-159 | ypbG | 2.7.1.2 | GK | ROK family | |
NHEFJLLP_00021 | 5.9e-287 | bgl | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_00022 | 1.2e-100 | U | Protein of unknown function DUF262 | |||
NHEFJLLP_00023 | 0.0 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
NHEFJLLP_00024 | 2.8e-252 | G | Major Facilitator | |||
NHEFJLLP_00025 | 5.4e-181 | K | Transcriptional regulator, LacI family | |||
NHEFJLLP_00026 | 1.8e-243 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
NHEFJLLP_00027 | 2.4e-291 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
NHEFJLLP_00028 | 2.3e-07 | |||||
NHEFJLLP_00029 | 7.7e-70 | 5.4.2.6 | S | Haloacid dehalogenase-like hydrolase | ||
NHEFJLLP_00030 | 7.8e-236 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
NHEFJLLP_00031 | 1.4e-222 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
NHEFJLLP_00032 | 9.1e-35 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NHEFJLLP_00034 | 1.1e-24 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
NHEFJLLP_00036 | 9.8e-43 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
NHEFJLLP_00037 | 1.5e-135 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
NHEFJLLP_00039 | 1.5e-188 | pts36C | G | PTS system sugar-specific permease component | ||
NHEFJLLP_00040 | 4.4e-40 | pts36C | G | PTS system sugar-specific permease component | ||
NHEFJLLP_00041 | 3.3e-52 | sgcB | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_00042 | 4.2e-80 | pts36A | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
NHEFJLLP_00043 | 2.8e-140 | K | DeoR C terminal sensor domain | |||
NHEFJLLP_00044 | 3.8e-179 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
NHEFJLLP_00045 | 1.6e-244 | iolF | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00046 | 1.8e-286 | rhaB | 2.7.1.12, 2.7.1.16, 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
NHEFJLLP_00047 | 4.2e-55 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
NHEFJLLP_00048 | 1.3e-256 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
NHEFJLLP_00049 | 4.6e-165 | rhaD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
NHEFJLLP_00050 | 1e-125 | S | Membrane | |||
NHEFJLLP_00051 | 1.6e-24 | yueI | S | Protein of unknown function (DUF1694) | ||
NHEFJLLP_00052 | 1.9e-26 | yueI | S | Protein of unknown function (DUF1694) | ||
NHEFJLLP_00053 | 8.6e-47 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
NHEFJLLP_00054 | 5.5e-183 | nrdF | 1.17.4.1 | F | Ribonucleotide reductase, small chain | |
NHEFJLLP_00055 | 1.1e-167 | nrdF | 1.17.4.1 | F | Ribonucleotide reductase, small chain | |
NHEFJLLP_00056 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NHEFJLLP_00057 | 1.4e-80 | nrdI | F | NrdI Flavodoxin like | ||
NHEFJLLP_00058 | 4.5e-59 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00059 | 1.3e-168 | D | nuclear chromosome segregation | |||
NHEFJLLP_00060 | 0.0 | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | ||
NHEFJLLP_00061 | 1.4e-303 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
NHEFJLLP_00062 | 2.2e-80 | hsdS_1 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
NHEFJLLP_00063 | 2e-38 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_00064 | 8.2e-51 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_00065 | 3.7e-34 | |||||
NHEFJLLP_00066 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NHEFJLLP_00067 | 0.0 | L | MobA MobL family protein | |||
NHEFJLLP_00068 | 2.5e-27 | |||||
NHEFJLLP_00069 | 3.1e-41 | |||||
NHEFJLLP_00070 | 3.1e-56 | tnp2PF3 | L | Transposase DDE domain | ||
NHEFJLLP_00071 | 2.4e-164 | corA | P | CorA-like Mg2+ transporter protein | ||
NHEFJLLP_00072 | 5.3e-37 | mntH | P | Natural resistance-associated macrophage protein | ||
NHEFJLLP_00073 | 2.6e-29 | |||||
NHEFJLLP_00074 | 3.7e-53 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
NHEFJLLP_00075 | 8.9e-66 | |||||
NHEFJLLP_00076 | 1.1e-43 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
NHEFJLLP_00077 | 4.7e-51 | repA | S | Replication initiator protein A | ||
NHEFJLLP_00078 | 3.3e-144 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_00079 | 3.8e-179 | yneE | K | Transcriptional regulator | ||
NHEFJLLP_00080 | 2.3e-75 | 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 | |
NHEFJLLP_00081 | 2.2e-179 | 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 | |
NHEFJLLP_00082 | 1.3e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NHEFJLLP_00083 | 1.1e-167 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
NHEFJLLP_00084 | 2.1e-126 | IQ | reductase | |||
NHEFJLLP_00085 | 1.6e-227 | 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 | |
NHEFJLLP_00086 | 2.3e-73 | 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 | |
NHEFJLLP_00087 | 6.1e-70 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
NHEFJLLP_00088 | 1.2e-260 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
NHEFJLLP_00089 | 1.5e-35 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
NHEFJLLP_00090 | 1.5e-35 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family | ||
NHEFJLLP_00091 | 1.8e-72 | |||||
NHEFJLLP_00092 | 3.6e-51 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
NHEFJLLP_00093 | 7.9e-26 | bcpA | 4.1.1.3 | G | Phosphoenolpyruvate phosphomutase | |
NHEFJLLP_00094 | 9.5e-92 | prpB | 4.1.3.30, 4.1.3.32 | G | Catalyzes the thermodynamically favored C-C bond cleavage of (2R,3S)-2-methylisocitrate to yield pyruvate and succinate | |
NHEFJLLP_00095 | 5.5e-125 | EGP | Sugar (and other) transporter | |||
NHEFJLLP_00096 | 1.1e-60 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00097 | 7.2e-77 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00098 | 2.6e-122 | S | Bacterial membrane protein, YfhO | |||
NHEFJLLP_00099 | 2.4e-43 | hsdS_1 | 3.1.21.3 | V | type I restriction modification DNA specificity domain protein | |
NHEFJLLP_00100 | 3.6e-124 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_00101 | 9.7e-46 | L | nucleotidyltransferase activity | |||
NHEFJLLP_00102 | 6.9e-31 | |||||
NHEFJLLP_00103 | 1.2e-109 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NHEFJLLP_00104 | 4.4e-46 | yktB | S | Belongs to the UPF0637 family | ||
NHEFJLLP_00105 | 8.3e-45 | yktB | S | Belongs to the UPF0637 family | ||
NHEFJLLP_00106 | 1.7e-37 | |||||
NHEFJLLP_00107 | 4.7e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
NHEFJLLP_00108 | 5.2e-289 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
NHEFJLLP_00109 | 1.3e-136 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
NHEFJLLP_00110 | 1.6e-123 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
NHEFJLLP_00111 | 6.1e-221 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
NHEFJLLP_00112 | 1.7e-137 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
NHEFJLLP_00113 | 1.6e-151 | pnuC | H | nicotinamide mononucleotide transporter | ||
NHEFJLLP_00114 | 4.4e-20 | plnB | 2.7.13.3 | T | GHKL domain | |
NHEFJLLP_00115 | 1.4e-40 | T | diguanylate cyclase | |||
NHEFJLLP_00116 | 5.3e-26 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
NHEFJLLP_00117 | 4.7e-154 | K | CAT RNA binding domain | |||
NHEFJLLP_00118 | 3.9e-84 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |||
NHEFJLLP_00119 | 4e-108 | glnP | P | ABC transporter permease | ||
NHEFJLLP_00120 | 1.6e-109 | gluC | P | ABC transporter permease | ||
NHEFJLLP_00121 | 7.8e-149 | glnH | ET | ABC transporter substrate-binding protein | ||
NHEFJLLP_00122 | 9e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NHEFJLLP_00124 | 1.4e-40 | |||||
NHEFJLLP_00125 | 4.3e-170 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NHEFJLLP_00126 | 3e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
NHEFJLLP_00127 | 8.8e-113 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
NHEFJLLP_00128 | 1.1e-50 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
NHEFJLLP_00129 | 2.5e-52 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
NHEFJLLP_00130 | 4.6e-108 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
NHEFJLLP_00131 | 2.2e-198 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NHEFJLLP_00132 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NHEFJLLP_00133 | 6.5e-37 | nrdH | O | Glutaredoxin | ||
NHEFJLLP_00134 | 3.4e-109 | rsmC | 2.1.1.172 | J | Methyltransferase | |
NHEFJLLP_00135 | 5.9e-91 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
NHEFJLLP_00136 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NHEFJLLP_00137 | 5.8e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
NHEFJLLP_00138 | 7.4e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
NHEFJLLP_00139 | 2.2e-38 | yaaL | S | Protein of unknown function (DUF2508) | ||
NHEFJLLP_00140 | 6.3e-29 | K | transcriptional regulator | |||
NHEFJLLP_00142 | 1.6e-144 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
NHEFJLLP_00143 | 1e-173 | 4.2.1.6, 5.1.2.2 | M | Mandelate racemase muconate lactonizing enzyme | ||
NHEFJLLP_00144 | 2.6e-138 | gntT | EG | Gluconate | ||
NHEFJLLP_00145 | 2.3e-161 | P | Sodium:sulfate symporter transmembrane region | |||
NHEFJLLP_00146 | 1.8e-125 | mcyI | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
NHEFJLLP_00147 | 1.7e-72 | K | LysR substrate binding domain | |||
NHEFJLLP_00148 | 4e-216 | gudD | 4.2.1.40 | M | Mandelate racemase / muconate lactonizing enzyme, C-terminal domain | |
NHEFJLLP_00149 | 9.3e-245 | 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 | |
NHEFJLLP_00150 | 1.6e-177 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
NHEFJLLP_00151 | 5.3e-217 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NHEFJLLP_00152 | 2.8e-29 | yajC | U | Preprotein translocase | ||
NHEFJLLP_00153 | 8.2e-226 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
NHEFJLLP_00154 | 6.3e-201 | 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) | |
NHEFJLLP_00155 | 2.1e-188 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
NHEFJLLP_00156 | 1e-105 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
NHEFJLLP_00157 | 5.1e-30 | K | LysR substrate binding domain | |||
NHEFJLLP_00158 | 1.9e-37 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
NHEFJLLP_00159 | 0.0 | S | membrane | |||
NHEFJLLP_00160 | 1.5e-54 | yneR | S | Belongs to the HesB IscA family | ||
NHEFJLLP_00161 | 4e-75 | XK27_02470 | K | LytTr DNA-binding domain | ||
NHEFJLLP_00162 | 7.3e-95 | liaI | S | membrane | ||
NHEFJLLP_00163 | 6.8e-81 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
NHEFJLLP_00164 | 2.6e-112 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
NHEFJLLP_00165 | 6.6e-186 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
NHEFJLLP_00166 | 5.1e-30 | K | LysR substrate binding domain | |||
NHEFJLLP_00168 | 6.8e-63 | lmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00169 | 3e-63 | lmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00171 | 1.3e-174 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
NHEFJLLP_00172 | 2e-100 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
NHEFJLLP_00173 | 1.1e-86 | gutM | K | Glucitol operon activator protein (GutM) | ||
NHEFJLLP_00174 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
NHEFJLLP_00175 | 3.8e-145 | IQ | NAD dependent epimerase/dehydratase family | |||
NHEFJLLP_00176 | 2.7e-160 | rbsU | U | ribose uptake protein RbsU | ||
NHEFJLLP_00177 | 7.9e-67 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
NHEFJLLP_00178 | 2.3e-162 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
NHEFJLLP_00179 | 5.9e-188 | rbsR | K | helix_turn _helix lactose operon repressor | ||
NHEFJLLP_00180 | 3.1e-101 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
NHEFJLLP_00181 | 8.3e-54 | K | Transcriptional regulator PadR-like family | |||
NHEFJLLP_00182 | 8.3e-54 | K | Transcriptional regulator PadR-like family | |||
NHEFJLLP_00184 | 1.1e-197 | yhhX | 1.1.1.371 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
NHEFJLLP_00185 | 1.3e-176 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHEFJLLP_00186 | 1.1e-110 | K | Helix-turn-helix domain, rpiR family | |||
NHEFJLLP_00187 | 2.3e-157 | ccpB | 5.1.1.1 | K | lacI family | |
NHEFJLLP_00188 | 8.8e-123 | S | Sucrose-6F-phosphate phosphohydrolase | |||
NHEFJLLP_00189 | 5e-146 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NHEFJLLP_00190 | 3.1e-178 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
NHEFJLLP_00191 | 1.6e-97 | drgA | C | Nitroreductase family | ||
NHEFJLLP_00192 | 3.6e-168 | S | Polyphosphate kinase 2 (PPK2) | |||
NHEFJLLP_00193 | 1e-10 | oppA | E | ABC transporter, substratebinding protein | ||
NHEFJLLP_00194 | 1e-10 | oppA | E | ABC transporter, substratebinding protein | ||
NHEFJLLP_00195 | 2.2e-120 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_00196 | 3.6e-88 | niaR | S | 3H domain | ||
NHEFJLLP_00197 | 6.6e-265 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
NHEFJLLP_00198 | 1.3e-117 | K | Transcriptional regulator | |||
NHEFJLLP_00199 | 1.2e-153 | V | ABC transporter | |||
NHEFJLLP_00200 | 8.2e-134 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NHEFJLLP_00201 | 3.1e-245 | dsdA | 4.3.1.18 | E | Belongs to the serine threonine dehydratase family. DsdA subfamily | |
NHEFJLLP_00202 | 1.8e-294 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_00203 | 2.8e-295 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_00204 | 1.8e-54 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
NHEFJLLP_00205 | 2.3e-48 | pts20B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_00206 | 1.8e-130 | gntR | K | UTRA | ||
NHEFJLLP_00207 | 6.8e-141 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
NHEFJLLP_00208 | 6.5e-122 | pgm7 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
NHEFJLLP_00209 | 1.8e-81 | |||||
NHEFJLLP_00210 | 9.8e-152 | S | hydrolase | |||
NHEFJLLP_00211 | 4.2e-181 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
NHEFJLLP_00212 | 8.3e-152 | EG | EamA-like transporter family | |||
NHEFJLLP_00213 | 5e-176 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
NHEFJLLP_00214 | 1.3e-100 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
NHEFJLLP_00215 | 8.2e-235 | |||||
NHEFJLLP_00216 | 1.1e-77 | fld | C | Flavodoxin | ||
NHEFJLLP_00217 | 0.0 | M | Bacterial Ig-like domain (group 3) | |||
NHEFJLLP_00218 | 3.3e-46 | M | Bacterial surface protein 26-residue PARCEL repeat (3 repeats) | |||
NHEFJLLP_00219 | 0.0 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
NHEFJLLP_00220 | 1.4e-164 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
NHEFJLLP_00221 | 8.9e-184 | aroF | 2.5.1.54 | E | DAHP synthetase I family | |
NHEFJLLP_00222 | 1.8e-165 | 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) | |
NHEFJLLP_00223 | 2.1e-19 | 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) | |
NHEFJLLP_00224 | 1.4e-262 | P | Sodium:sulfate symporter transmembrane region | |||
NHEFJLLP_00225 | 4.1e-53 | yitW | S | Iron-sulfur cluster assembly protein | ||
NHEFJLLP_00226 | 4.1e-115 | ttdB | 4.2.1.2, 4.2.1.32 | C | Catalyzes the reversible hydration of fumarate to (S)- malate | |
NHEFJLLP_00227 | 4.4e-177 | ttdA | 4.2.1.32 | C | Fumarate hydratase (Fumerase) | |
NHEFJLLP_00228 | 2.2e-75 | L | Integrase core domain | |||
NHEFJLLP_00229 | 1.4e-49 | |||||
NHEFJLLP_00230 | 1.6e-48 | |||||
NHEFJLLP_00231 | 3.1e-128 | cycA | E | Amino acid permease | ||
NHEFJLLP_00232 | 1.2e-255 | nhaC | C | Na H antiporter NhaC | ||
NHEFJLLP_00233 | 2.1e-27 | 3.2.2.10 | S | Belongs to the LOG family | ||
NHEFJLLP_00234 | 1.3e-199 | frlB | M | SIS domain | ||
NHEFJLLP_00235 | 0.0 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
NHEFJLLP_00236 | 2e-219 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NHEFJLLP_00237 | 4.8e-125 | yyaQ | S | YjbR | ||
NHEFJLLP_00239 | 3.2e-40 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
NHEFJLLP_00240 | 3.3e-66 | V | CAAX protease self-immunity | |||
NHEFJLLP_00241 | 1.4e-64 | V | CAAX protease self-immunity | |||
NHEFJLLP_00242 | 3.2e-15 | S | Protein of unknown function (DUF554) | |||
NHEFJLLP_00243 | 3.2e-15 | S | Protein of unknown function (DUF554) | |||
NHEFJLLP_00244 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
NHEFJLLP_00245 | 3.5e-129 | treR | K | UTRA | ||
NHEFJLLP_00246 | 1.7e-42 | |||||
NHEFJLLP_00247 | 7.3e-43 | S | Protein of unknown function (DUF2089) | |||
NHEFJLLP_00248 | 4.3e-141 | pnuC | H | nicotinamide mononucleotide transporter | ||
NHEFJLLP_00249 | 1.7e-158 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
NHEFJLLP_00250 | 4.5e-166 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
NHEFJLLP_00251 | 9.8e-211 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
NHEFJLLP_00252 | 2e-52 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_00253 | 1.1e-25 | S | membrane transporter protein | |||
NHEFJLLP_00254 | 1.7e-17 | pts23C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_00255 | 7e-53 | ptcB | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_00256 | 6.8e-75 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
NHEFJLLP_00257 | 2.6e-149 | dicA | K | Helix-turn-helix domain | ||
NHEFJLLP_00258 | 7.2e-55 | |||||
NHEFJLLP_00259 | 3.4e-160 | T | Calcineurin-like phosphoesterase superfamily domain | |||
NHEFJLLP_00260 | 7.4e-64 | |||||
NHEFJLLP_00261 | 0.0 | P | Concanavalin A-like lectin/glucanases superfamily | |||
NHEFJLLP_00263 | 9.9e-177 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
NHEFJLLP_00266 | 1.3e-23 | S | Short C-terminal domain | |||
NHEFJLLP_00268 | 8.8e-25 | S | Short C-terminal domain | |||
NHEFJLLP_00270 | 2.9e-43 | L | HTH-like domain | |||
NHEFJLLP_00271 | 3.4e-36 | L | transposase activity | |||
NHEFJLLP_00272 | 3.8e-61 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_00276 | 6.5e-78 | elaA | S | GNAT family | ||
NHEFJLLP_00277 | 8.9e-184 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
NHEFJLLP_00278 | 0.0 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
NHEFJLLP_00279 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
NHEFJLLP_00280 | 3.9e-75 | yjcF | S | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_00281 | 1.6e-76 | elaA | S | GNAT family | ||
NHEFJLLP_00282 | 6.6e-44 | 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 | |
NHEFJLLP_00283 | 6e-45 | 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 | |
NHEFJLLP_00284 | 4.1e-66 | S | CAAX protease self-immunity | |||
NHEFJLLP_00285 | 2.5e-59 | |||||
NHEFJLLP_00286 | 4.5e-55 | |||||
NHEFJLLP_00287 | 1.6e-137 | pltR | K | LytTr DNA-binding domain | ||
NHEFJLLP_00288 | 1.1e-223 | pltK | 2.7.13.3 | T | GHKL domain | |
NHEFJLLP_00289 | 1.7e-108 | |||||
NHEFJLLP_00290 | 2.2e-148 | S | Sucrose-6F-phosphate phosphohydrolase | |||
NHEFJLLP_00291 | 2.1e-158 | ypaH | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
NHEFJLLP_00292 | 1.8e-104 | GM | NAD(P)H-binding | |||
NHEFJLLP_00293 | 1.6e-64 | K | helix_turn_helix, mercury resistance | |||
NHEFJLLP_00294 | 1.2e-154 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
NHEFJLLP_00295 | 1.1e-37 | 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 | |
NHEFJLLP_00296 | 1.5e-62 | ydaO | E | amino acid | ||
NHEFJLLP_00297 | 2.1e-31 | |||||
NHEFJLLP_00298 | 3.7e-42 | dinB | 2.7.7.7 | L | impB/mucB/samB family C-terminal domain | |
NHEFJLLP_00299 | 1.6e-134 | K | response regulator | |||
NHEFJLLP_00300 | 3e-243 | XK27_08635 | S | UPF0210 protein | ||
NHEFJLLP_00301 | 2.3e-38 | gcvR | T | Belongs to the UPF0237 family | ||
NHEFJLLP_00302 | 1.5e-169 | EG | EamA-like transporter family | |||
NHEFJLLP_00304 | 7.7e-92 | S | ECF-type riboflavin transporter, S component | |||
NHEFJLLP_00305 | 8.6e-48 | |||||
NHEFJLLP_00306 | 2.2e-213 | yceI | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00307 | 9.4e-138 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
NHEFJLLP_00308 | 1.4e-22 | |||||
NHEFJLLP_00310 | 2.2e-78 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
NHEFJLLP_00311 | 5.8e-79 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
NHEFJLLP_00312 | 1.6e-26 | lldP | C | L-lactate permease | ||
NHEFJLLP_00313 | 1.1e-167 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
NHEFJLLP_00314 | 4e-229 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
NHEFJLLP_00315 | 1.3e-176 | |||||
NHEFJLLP_00316 | 3.3e-132 | cobB | K | SIR2 family | ||
NHEFJLLP_00317 | 2e-160 | yunF | F | Protein of unknown function DUF72 | ||
NHEFJLLP_00318 | 2.6e-70 | mutT | 3.6.1.55 | F | DNA mismatch repair protein MutT | |
NHEFJLLP_00319 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
NHEFJLLP_00321 | 2.8e-162 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
NHEFJLLP_00322 | 1.1e-256 | adhE | 1.1.1.1, 1.2.1.10 | C | Aldehyde dehydrogenase family | |
NHEFJLLP_00323 | 4.9e-190 | |||||
NHEFJLLP_00324 | 2e-163 | ytrB | V | ABC transporter | ||
NHEFJLLP_00325 | 1.4e-59 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
NHEFJLLP_00326 | 8.1e-22 | |||||
NHEFJLLP_00327 | 1.5e-89 | K | acetyltransferase | |||
NHEFJLLP_00328 | 3e-84 | K | GNAT family | |||
NHEFJLLP_00329 | 1.1e-83 | 6.3.3.2 | S | ASCH | ||
NHEFJLLP_00330 | 5e-96 | puuR | K | Cupin domain | ||
NHEFJLLP_00331 | 2.6e-22 | celD | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_00333 | 6.1e-141 | E | IrrE N-terminal-like domain | |||
NHEFJLLP_00334 | 3.4e-19 | S | Domain of unknown function (DUF4411) | |||
NHEFJLLP_00336 | 3.5e-60 | S | Terminase small subunit | |||
NHEFJLLP_00337 | 6.7e-187 | S | Phage terminase, large subunit, PBSX family | |||
NHEFJLLP_00338 | 4.1e-114 | S | Phage portal protein, SPP1 Gp6-like | |||
NHEFJLLP_00339 | 4.8e-45 | S | Phage minor capsid protein 2 | |||
NHEFJLLP_00341 | 3.7e-107 | |||||
NHEFJLLP_00343 | 2.3e-13 | |||||
NHEFJLLP_00346 | 1.1e-10 | S | Minor capsid protein from bacteriophage | |||
NHEFJLLP_00347 | 2.7e-42 | N | domain, Protein | |||
NHEFJLLP_00349 | 8.1e-13 | S | Bacteriophage Gp15 protein | |||
NHEFJLLP_00350 | 1.1e-166 | M | Phage tail tape measure protein TP901 | |||
NHEFJLLP_00351 | 1.7e-47 | S | Phage tail protein | |||
NHEFJLLP_00352 | 1.5e-99 | S | Prophage endopeptidase tail | |||
NHEFJLLP_00354 | 2.3e-08 | |||||
NHEFJLLP_00355 | 1.1e-81 | S | Calcineurin-like phosphoesterase | |||
NHEFJLLP_00359 | 2.1e-36 | |||||
NHEFJLLP_00362 | 3.5e-168 | M | hydrolase, family 25 | |||
NHEFJLLP_00364 | 2.3e-173 | kup | P | Transport of potassium into the cell | ||
NHEFJLLP_00365 | 2.9e-193 | P | ABC transporter, substratebinding protein | |||
NHEFJLLP_00366 | 2.2e-129 | ssuC2 | U | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_00367 | 5e-134 | P | ATPases associated with a variety of cellular activities | |||
NHEFJLLP_00368 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
NHEFJLLP_00369 | 3.7e-204 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
NHEFJLLP_00370 | 3.3e-35 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
NHEFJLLP_00371 | 1e-41 | S | Plasmid replication protein | |||
NHEFJLLP_00372 | 1.1e-120 | |||||
NHEFJLLP_00373 | 6.5e-33 | |||||
NHEFJLLP_00376 | 1.7e-118 | |||||
NHEFJLLP_00377 | 1.5e-107 | dam | 2.1.1.72 | H | Site-specific DNA-methyltransferase (adenine-specific) | |
NHEFJLLP_00378 | 1.8e-56 | S | Protein of unknown function, DUF536 | |||
NHEFJLLP_00379 | 6.9e-162 | L | Initiator Replication protein | |||
NHEFJLLP_00380 | 3.1e-10 | XK27_07075 | S | CAAX protease self-immunity | ||
NHEFJLLP_00382 | 4.9e-31 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NHEFJLLP_00383 | 5.2e-156 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
NHEFJLLP_00384 | 1.7e-98 | metI | P | ABC transporter permease | ||
NHEFJLLP_00385 | 7e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NHEFJLLP_00387 | 1.3e-128 | dnaD | L | Replication initiation and membrane attachment | ||
NHEFJLLP_00388 | 5.4e-258 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
NHEFJLLP_00389 | 4.3e-225 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
NHEFJLLP_00390 | 2.1e-72 | ypmB | S | protein conserved in bacteria | ||
NHEFJLLP_00391 | 5e-187 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
NHEFJLLP_00392 | 4.3e-62 | mdtH | P | Sugar (and other) transporter | ||
NHEFJLLP_00393 | 3.1e-60 | mdtH | P | Sugar (and other) transporter | ||
NHEFJLLP_00394 | 1.1e-30 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NHEFJLLP_00395 | 3e-53 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
NHEFJLLP_00396 | 2.4e-50 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
NHEFJLLP_00397 | 1.5e-256 | glnP | P | ABC transporter | ||
NHEFJLLP_00398 | 1.2e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NHEFJLLP_00399 | 4.6e-105 | yxjI | ||||
NHEFJLLP_00400 | 4.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
NHEFJLLP_00401 | 1.6e-136 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
NHEFJLLP_00402 | 1.4e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
NHEFJLLP_00403 | 5e-81 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
NHEFJLLP_00404 | 1.8e-87 | 2.3.1.128, 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_00405 | 1.1e-100 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
NHEFJLLP_00406 | 1.5e-38 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
NHEFJLLP_00407 | 5.8e-38 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
NHEFJLLP_00408 | 5.9e-54 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
NHEFJLLP_00409 | 4.5e-26 | S | Protein of unknown function | |||
NHEFJLLP_00410 | 3.5e-08 | |||||
NHEFJLLP_00411 | 1.3e-18 | |||||
NHEFJLLP_00412 | 6.7e-35 | S | Transcriptional regulator, RinA family | |||
NHEFJLLP_00417 | 1.6e-56 | V | HNH nucleases | |||
NHEFJLLP_00418 | 1.3e-39 | L | Phage terminase, small subunit | |||
NHEFJLLP_00419 | 3.8e-48 | S | overlaps another CDS with the same product name | |||
NHEFJLLP_00420 | 1.9e-203 | S | Phage Terminase | |||
NHEFJLLP_00422 | 2.2e-86 | S | Phage portal protein | |||
NHEFJLLP_00423 | 6.1e-46 | S | Phage portal protein | |||
NHEFJLLP_00424 | 3.8e-45 | S | Phage derived protein Gp49-like (DUF891) | |||
NHEFJLLP_00426 | 3.2e-228 | rodA | D | Cell cycle protein | ||
NHEFJLLP_00427 | 0.0 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_00428 | 7.9e-143 | P | ATPases associated with a variety of cellular activities | |||
NHEFJLLP_00429 | 1.1e-220 | lytR5 | K | Cell envelope-related transcriptional attenuator domain | ||
NHEFJLLP_00430 | 2.7e-100 | L | Helix-turn-helix domain | |||
NHEFJLLP_00431 | 1.5e-177 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
NHEFJLLP_00432 | 1.1e-50 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
NHEFJLLP_00433 | 2.1e-263 | 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 | |
NHEFJLLP_00434 | 2.3e-165 | 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 | ||
NHEFJLLP_00435 | 2.7e-280 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
NHEFJLLP_00436 | 1.8e-90 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NHEFJLLP_00437 | 6e-51 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
NHEFJLLP_00438 | 2.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NHEFJLLP_00439 | 6.5e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
NHEFJLLP_00440 | 5e-232 | pyrP | F | Permease | ||
NHEFJLLP_00441 | 1.5e-39 | K | transcriptional regulator, MerR family | |||
NHEFJLLP_00442 | 3.4e-61 | rfbP | M | Bacterial sugar transferase | ||
NHEFJLLP_00443 | 3.4e-61 | rfbP | M | Bacterial sugar transferase | ||
NHEFJLLP_00444 | 3e-50 | GM | epimerase | |||
NHEFJLLP_00445 | 2.7e-51 | GM | epimerase | |||
NHEFJLLP_00446 | 4.8e-15 | |||||
NHEFJLLP_00447 | 7.1e-65 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
NHEFJLLP_00448 | 1.1e-65 | |||||
NHEFJLLP_00449 | 2.3e-47 | |||||
NHEFJLLP_00450 | 1.2e-155 | L | DnaD domain protein | |||
NHEFJLLP_00451 | 8.1e-13 | S | Domain of unknown function (DUF1508) | |||
NHEFJLLP_00452 | 1.1e-76 | |||||
NHEFJLLP_00455 | 5.8e-26 | K | Cro/C1-type HTH DNA-binding domain | |||
NHEFJLLP_00456 | 1.7e-37 | K | sequence-specific DNA binding | |||
NHEFJLLP_00459 | 5.2e-18 | K | sequence-specific DNA binding | |||
NHEFJLLP_00460 | 6.1e-09 | S | Pfam:Peptidase_M78 | |||
NHEFJLLP_00461 | 8.5e-11 | S | DNA/RNA non-specific endonuclease | |||
NHEFJLLP_00464 | 1.6e-24 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
NHEFJLLP_00465 | 6.2e-55 | bcr1 | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00467 | 6.6e-258 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
NHEFJLLP_00468 | 1.2e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
NHEFJLLP_00469 | 3.7e-145 | |||||
NHEFJLLP_00470 | 2.1e-139 | htpX | O | Belongs to the peptidase M48B family | ||
NHEFJLLP_00471 | 1.7e-91 | lemA | S | LemA family | ||
NHEFJLLP_00472 | 9.2e-127 | srtA | 3.4.22.70 | M | sortase family | |
NHEFJLLP_00473 | 9.4e-214 | J | translation release factor activity | |||
NHEFJLLP_00474 | 7.8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
NHEFJLLP_00475 | 3.8e-51 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NHEFJLLP_00476 | 8.4e-51 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NHEFJLLP_00477 | 1e-132 | 2.7.7.65 | T | diguanylate cyclase activity | ||
NHEFJLLP_00478 | 0.0 | ydaN | S | Bacterial cellulose synthase subunit | ||
NHEFJLLP_00479 | 2.8e-216 | ydaM | M | Glycosyl transferase family group 2 | ||
NHEFJLLP_00480 | 1e-205 | S | Protein conserved in bacteria | |||
NHEFJLLP_00481 | 1.2e-245 | |||||
NHEFJLLP_00482 | 1.5e-163 | G | Belongs to the glycosyl hydrolase 8 (cellulase D) family | |||
NHEFJLLP_00483 | 8e-13 | |||||
NHEFJLLP_00484 | 3.9e-22 | chpA | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
NHEFJLLP_00485 | 3.7e-20 | T | SpoVT / AbrB like domain | |||
NHEFJLLP_00486 | 7.5e-27 | hol | S | Bacteriophage holin | ||
NHEFJLLP_00487 | 4.3e-43 | |||||
NHEFJLLP_00488 | 6.9e-161 | M | hydrolase, family 25 | |||
NHEFJLLP_00492 | 3.1e-83 | S | Calcineurin-like phosphoesterase | |||
NHEFJLLP_00495 | 1.5e-198 | 3.4.14.13 | M | Prophage endopeptidase tail | ||
NHEFJLLP_00496 | 4.4e-158 | S | Phage tail protein | |||
NHEFJLLP_00497 | 0.0 | D | NLP P60 protein | |||
NHEFJLLP_00499 | 6.8e-87 | S | Phage tail assembly chaperone protein, TAC | |||
NHEFJLLP_00500 | 7.5e-90 | |||||
NHEFJLLP_00501 | 2.6e-59 | |||||
NHEFJLLP_00502 | 6.2e-94 | |||||
NHEFJLLP_00503 | 5.4e-49 | |||||
NHEFJLLP_00504 | 4.1e-54 | S | Phage gp6-like head-tail connector protein | |||
NHEFJLLP_00505 | 3.5e-194 | gpG | ||||
NHEFJLLP_00506 | 1.1e-54 | S | Domain of unknown function (DUF4355) | |||
NHEFJLLP_00507 | 5.3e-162 | S | Phage Mu protein F like protein | |||
NHEFJLLP_00508 | 6.9e-306 | S | Phage portal protein, SPP1 Gp6-like | |||
NHEFJLLP_00509 | 5.6e-255 | S | Phage terminase, large subunit | |||
NHEFJLLP_00510 | 1.1e-65 | ps333 | L | Terminase small subunit | ||
NHEFJLLP_00511 | 5.8e-14 | |||||
NHEFJLLP_00512 | 3.2e-49 | S | Predicted membrane protein (DUF2335) | |||
NHEFJLLP_00515 | 6.3e-197 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
NHEFJLLP_00516 | 3.1e-278 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
NHEFJLLP_00517 | 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 |
NHEFJLLP_00518 | 0.0 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
NHEFJLLP_00520 | 7.6e-143 | S | haloacid dehalogenase-like hydrolase | |||
NHEFJLLP_00521 | 2.1e-17 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
NHEFJLLP_00522 | 4.3e-62 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
NHEFJLLP_00523 | 6.8e-37 | lmrA | 3.6.3.44 | V | ABC transporter | |
NHEFJLLP_00524 | 7.6e-46 | ybiR | P | Citrate transporter | ||
NHEFJLLP_00525 | 6.6e-89 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
NHEFJLLP_00526 | 8e-235 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
NHEFJLLP_00527 | 1.6e-227 | 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 | |
NHEFJLLP_00528 | 1.7e-218 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
NHEFJLLP_00530 | 0.0 | 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 | ||
NHEFJLLP_00531 | 4.2e-80 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
NHEFJLLP_00532 | 3.1e-107 | 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 | ||
NHEFJLLP_00533 | 2.3e-69 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
NHEFJLLP_00534 | 2.3e-164 | ptlF | S | KR domain | ||
NHEFJLLP_00535 | 1.1e-74 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
NHEFJLLP_00536 | 1e-72 | C | FMN binding | |||
NHEFJLLP_00537 | 1.1e-156 | K | LysR family | |||
NHEFJLLP_00538 | 4.5e-258 | P | Sodium:sulfate symporter transmembrane region | |||
NHEFJLLP_00539 | 0.0 | nqr | 1.3.5.4, 1.5.1.36 | C | FMN_bind | |
NHEFJLLP_00540 | 7.1e-98 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_00541 | 2.5e-231 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
NHEFJLLP_00542 | 2.9e-78 | 3.6.1.55 | F | NUDIX domain | ||
NHEFJLLP_00543 | 1.3e-48 | sugE | U | Multidrug resistance protein | ||
NHEFJLLP_00544 | 1.2e-26 | |||||
NHEFJLLP_00545 | 2.1e-128 | pgm3 | G | Phosphoglycerate mutase family | ||
NHEFJLLP_00546 | 4.7e-125 | pgm3 | G | Phosphoglycerate mutase family | ||
NHEFJLLP_00547 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
NHEFJLLP_00548 | 7.1e-52 | yqkA | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
NHEFJLLP_00549 | 9.9e-35 | pts14C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_00550 | 5e-29 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
NHEFJLLP_00551 | 1e-72 | S | COG NOG18757 non supervised orthologous group | |||
NHEFJLLP_00552 | 2.8e-247 | lmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00553 | 3.4e-25 | |||||
NHEFJLLP_00554 | 1.1e-49 | |||||
NHEFJLLP_00555 | 9.4e-65 | ycgX | S | Protein of unknown function (DUF1398) | ||
NHEFJLLP_00556 | 9.1e-251 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
NHEFJLLP_00557 | 5.9e-214 | mdtG | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00558 | 7.6e-180 | D | Alpha beta | |||
NHEFJLLP_00559 | 3.1e-78 | M1-874 | K | Domain of unknown function (DUF1836) | ||
NHEFJLLP_00560 | 5e-29 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
NHEFJLLP_00561 | 1.8e-49 | L | Transposase | |||
NHEFJLLP_00562 | 2.5e-32 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
NHEFJLLP_00563 | 2.5e-32 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
NHEFJLLP_00564 | 9e-57 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
NHEFJLLP_00565 | 3.3e-67 | GM | NAD(P)H-binding | |||
NHEFJLLP_00566 | 4.7e-93 | S | Phosphatidylethanolamine-binding protein | |||
NHEFJLLP_00567 | 2.3e-77 | yphH | S | Cupin domain | ||
NHEFJLLP_00568 | 3.7e-60 | I | sulfurtransferase activity | |||
NHEFJLLP_00569 | 1.9e-138 | IQ | reductase | |||
NHEFJLLP_00570 | 1.2e-115 | GM | NAD(P)H-binding | |||
NHEFJLLP_00571 | 8.6e-218 | ykiI | ||||
NHEFJLLP_00572 | 0.0 | V | ABC transporter | |||
NHEFJLLP_00573 | 4.8e-311 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_00574 | 3.6e-58 | 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 | |
NHEFJLLP_00575 | 1.3e-122 | yliE | T | EAL domain | ||
NHEFJLLP_00576 | 6.4e-148 | 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | ||
NHEFJLLP_00577 | 7e-104 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_00578 | 1.2e-207 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
NHEFJLLP_00579 | 1.5e-52 | |||||
NHEFJLLP_00580 | 3e-72 | |||||
NHEFJLLP_00581 | 3e-131 | 1.5.1.39 | C | nitroreductase | ||
NHEFJLLP_00583 | 1.6e-129 | K | UbiC transcription regulator-associated domain protein | |||
NHEFJLLP_00585 | 1.2e-97 | S | UPF0397 protein | |||
NHEFJLLP_00586 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
NHEFJLLP_00587 | 4.9e-151 | cbiQ | P | cobalt transport | ||
NHEFJLLP_00588 | 4e-209 | C | Oxidoreductase | |||
NHEFJLLP_00589 | 2.6e-259 | |||||
NHEFJLLP_00590 | 1.9e-41 | endA | F | DNA RNA non-specific endonuclease | ||
NHEFJLLP_00591 | 7e-19 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_00592 | 4.2e-41 | K | helix_turn_helix, arabinose operon control protein | |||
NHEFJLLP_00593 | 4.9e-62 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_00594 | 3.5e-208 | M | Glycosyl transferase family 2 | |||
NHEFJLLP_00595 | 1.9e-71 | |||||
NHEFJLLP_00596 | 5.3e-95 | K | Crp-like helix-turn-helix domain | |||
NHEFJLLP_00597 | 1.3e-148 | S | Uncharacterised protein, DegV family COG1307 | |||
NHEFJLLP_00598 | 1.8e-84 | M1-874 | K | Domain of unknown function (DUF1836) | ||
NHEFJLLP_00599 | 5e-210 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
NHEFJLLP_00600 | 1.5e-183 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
NHEFJLLP_00601 | 8.7e-80 | bioY | S | BioY family | ||
NHEFJLLP_00602 | 3.4e-100 | S | Permuted papain-like amidase enzyme, YaeF/YiiX, C92 family | |||
NHEFJLLP_00603 | 4.5e-63 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_00604 | 3e-14 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
NHEFJLLP_00605 | 5.4e-44 | endA | F | DNA RNA non-specific endonuclease | ||
NHEFJLLP_00606 | 1.1e-29 | S | Prolyl oligopeptidase family | |||
NHEFJLLP_00607 | 1.1e-29 | S | Prolyl oligopeptidase family | |||
NHEFJLLP_00608 | 4.6e-14 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00609 | 3.7e-18 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00611 | 2.6e-177 | yhgE | V | domain protein | ||
NHEFJLLP_00612 | 5.9e-62 | K | Transcriptional regulator (TetR family) | |||
NHEFJLLP_00613 | 4.9e-54 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NHEFJLLP_00614 | 2.1e-81 | L | COG3547 Transposase and inactivated derivatives | |||
NHEFJLLP_00615 | 5.6e-95 | tnpR1 | L | Resolvase, N terminal domain | ||
NHEFJLLP_00617 | 1.6e-09 | L | Integrase | |||
NHEFJLLP_00618 | 3e-11 | L | Integrase | |||
NHEFJLLP_00619 | 4.5e-42 | T | Antidote-toxin recognition MazE, bacterial antitoxin | |||
NHEFJLLP_00620 | 2.5e-53 | pemK | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
NHEFJLLP_00621 | 6.9e-61 | ydeN | S | Serine hydrolase | ||
NHEFJLLP_00622 | 5.3e-82 | yjbB | G | Permeases of the major facilitator superfamily | ||
NHEFJLLP_00623 | 1.8e-43 | XK27_04650 | K | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_00624 | 8.2e-32 | S | SnoaL-like polyketide cyclase | |||
NHEFJLLP_00625 | 2e-49 | K | Acetyltransferase (GNAT) domain | |||
NHEFJLLP_00626 | 2e-07 | K | transcriptional regulator | |||
NHEFJLLP_00627 | 3.1e-57 | MA20_27515 | EGP | PFAM Major Facilitator Superfamily | ||
NHEFJLLP_00628 | 1.1e-39 | MA20_27515 | EGP | Major Facilitator Superfamily | ||
NHEFJLLP_00629 | 1.2e-18 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_00630 | 6.9e-114 | Q | Imidazolonepropionase and related amidohydrolases | |||
NHEFJLLP_00631 | 7.1e-44 | S | Protein of unknown function (DUF554) | |||
NHEFJLLP_00632 | 6.8e-179 | galR | K | Periplasmic binding protein-like domain | ||
NHEFJLLP_00633 | 3.5e-47 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
NHEFJLLP_00634 | 1.4e-173 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
NHEFJLLP_00635 | 1.8e-67 | S | Domain of unknown function (DUF3284) | |||
NHEFJLLP_00636 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
NHEFJLLP_00637 | 0.0 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
NHEFJLLP_00638 | 2.8e-28 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
NHEFJLLP_00639 | 1.4e-133 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
NHEFJLLP_00640 | 2.9e-179 | proV | E | ABC transporter, ATP-binding protein | ||
NHEFJLLP_00641 | 2.2e-254 | gshR | 1.8.1.7 | C | Glutathione reductase | |
NHEFJLLP_00642 | 1.3e-300 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
NHEFJLLP_00643 | 0.0 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
NHEFJLLP_00644 | 8e-134 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_00645 | 9.5e-46 | |||||
NHEFJLLP_00646 | 1.5e-52 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase family | |
NHEFJLLP_00647 | 2.9e-51 | XK27_09665 | 5.4.2.11 | G | Phosphoglycerate mutase family | |
NHEFJLLP_00648 | 1.7e-101 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_00649 | 9.2e-187 | S | Cell surface protein | |||
NHEFJLLP_00650 | 3.8e-75 | |||||
NHEFJLLP_00651 | 3.2e-262 | |||||
NHEFJLLP_00652 | 1e-227 | hpk9 | 2.7.13.3 | T | GHKL domain | |
NHEFJLLP_00653 | 2.9e-38 | S | TfoX C-terminal domain | |||
NHEFJLLP_00654 | 1.9e-138 | K | Helix-turn-helix domain | |||
NHEFJLLP_00655 | 3.1e-40 | GM | NmrA-like family | |||
NHEFJLLP_00656 | 1.6e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
NHEFJLLP_00657 | 9.8e-219 | ylbM | S | Belongs to the UPF0348 family | ||
NHEFJLLP_00658 | 4.4e-140 | yqeM | Q | Methyltransferase | ||
NHEFJLLP_00659 | 2.1e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
NHEFJLLP_00660 | 9.3e-115 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
NHEFJLLP_00661 | 1.4e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
NHEFJLLP_00662 | 1.1e-50 | yhbY | J | RNA-binding protein | ||
NHEFJLLP_00663 | 4.5e-216 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
NHEFJLLP_00664 | 1.4e-98 | yqeG | S | HAD phosphatase, family IIIA | ||
NHEFJLLP_00665 | 4.8e-41 | GM | NmrA-like family | |||
NHEFJLLP_00667 | 4.2e-16 | |||||
NHEFJLLP_00668 | 1.5e-07 | |||||
NHEFJLLP_00669 | 1.1e-21 | |||||
NHEFJLLP_00670 | 4.8e-69 | |||||
NHEFJLLP_00671 | 2.8e-47 | U | nuclease activity | |||
NHEFJLLP_00672 | 4.8e-20 | |||||
NHEFJLLP_00673 | 3.3e-29 | |||||
NHEFJLLP_00674 | 4.3e-100 | ankB | S | ankyrin repeats | ||
NHEFJLLP_00675 | 8.1e-08 | S | Immunity protein 22 | |||
NHEFJLLP_00676 | 8.5e-173 | |||||
NHEFJLLP_00677 | 4.4e-25 | S | Immunity protein 74 | |||
NHEFJLLP_00678 | 2.8e-52 | U | domain, Protein | |||
NHEFJLLP_00681 | 0.0 | ydgH | S | MMPL family | ||
NHEFJLLP_00682 | 3.2e-112 | S | Protein of unknown function (DUF1211) | |||
NHEFJLLP_00683 | 3.7e-34 | |||||
NHEFJLLP_00684 | 5.9e-185 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
NHEFJLLP_00685 | 8e-199 | 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 | |
NHEFJLLP_00686 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
NHEFJLLP_00687 | 2.8e-207 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
NHEFJLLP_00688 | 3.3e-89 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NHEFJLLP_00689 | 2e-174 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NHEFJLLP_00690 | 4.4e-74 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
NHEFJLLP_00691 | 1.8e-242 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
NHEFJLLP_00692 | 8.5e-50 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
NHEFJLLP_00693 | 1.2e-48 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
NHEFJLLP_00694 | 8.4e-51 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_00695 | 2.7e-49 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_00696 | 3e-30 | |||||
NHEFJLLP_00697 | 3.8e-93 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_00699 | 1.1e-37 | S | KilA-N domain | |||
NHEFJLLP_00702 | 5.2e-23 | S | Short C-terminal domain | |||
NHEFJLLP_00703 | 2.4e-08 | E | Zn peptidase | |||
NHEFJLLP_00705 | 3.1e-19 | 3.4.21.88 | K | Transcriptional | ||
NHEFJLLP_00707 | 5e-22 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
NHEFJLLP_00708 | 7.3e-81 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
NHEFJLLP_00709 | 9.8e-34 | isp | L | Transposase | ||
NHEFJLLP_00710 | 3.6e-100 | K | Transcriptional regulator, AbiEi antitoxin | |||
NHEFJLLP_00711 | 4.6e-41 | L | HIRAN domain | |||
NHEFJLLP_00712 | 6.7e-170 | yjjC | V | ABC transporter | ||
NHEFJLLP_00713 | 1.4e-298 | M | Exporter of polyketide antibiotics | |||
NHEFJLLP_00714 | 1.2e-115 | K | Transcriptional regulator | |||
NHEFJLLP_00715 | 1.2e-275 | C | Electron transfer flavoprotein FAD-binding domain | |||
NHEFJLLP_00716 | 8.6e-74 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
NHEFJLLP_00717 | 1.1e-92 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_00718 | 9e-147 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
NHEFJLLP_00719 | 1.4e-38 | yhcA | V | MacB-like periplasmic core domain | ||
NHEFJLLP_00720 | 4.5e-30 | yhcA | V | MacB-like periplasmic core domain | ||
NHEFJLLP_00721 | 1.7e-51 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
NHEFJLLP_00722 | 2.4e-141 | |||||
NHEFJLLP_00724 | 1e-142 | 2.7.7.47 | H | Mediates bacterial resistance to the antibiotics streptomycin and spectomycin | ||
NHEFJLLP_00725 | 4.8e-40 | |||||
NHEFJLLP_00726 | 2.7e-129 | cbiO | P | ABC transporter | ||
NHEFJLLP_00727 | 4.5e-149 | P | Cobalt transport protein | |||
NHEFJLLP_00728 | 3.1e-181 | nikMN | P | PDGLE domain | ||
NHEFJLLP_00729 | 4.2e-121 | K | Crp-like helix-turn-helix domain | |||
NHEFJLLP_00731 | 1.7e-51 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
NHEFJLLP_00732 | 4e-56 | |||||
NHEFJLLP_00733 | 6.7e-148 | levD | G | PTS system mannose/fructose/sorbose family IID component | ||
NHEFJLLP_00734 | 3.5e-136 | M | PTS system sorbose-specific iic component | |||
NHEFJLLP_00735 | 1.4e-89 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
NHEFJLLP_00736 | 1.8e-72 | levA | G | PTS system fructose IIA component | ||
NHEFJLLP_00737 | 0.0 | K | Sigma-54 interaction domain | |||
NHEFJLLP_00738 | 1.3e-10 | S | FRG | |||
NHEFJLLP_00739 | 4.7e-10 | S | Protein of unknown function, DUF536 | |||
NHEFJLLP_00740 | 2.7e-140 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00743 | 1.7e-09 | ptrA | S | Belongs to the peptidase M16 family | ||
NHEFJLLP_00749 | 6.2e-143 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
NHEFJLLP_00750 | 4.6e-33 | |||||
NHEFJLLP_00751 | 1.6e-21 | |||||
NHEFJLLP_00752 | 1.7e-127 | repA | S | Replication initiator protein A | ||
NHEFJLLP_00753 | 3.3e-21 | |||||
NHEFJLLP_00754 | 1.1e-40 | S | Bacterial epsilon antitoxin | |||
NHEFJLLP_00755 | 5.6e-156 | 2.7.1.176 | S | Zeta toxin | ||
NHEFJLLP_00756 | 7.4e-16 | |||||
NHEFJLLP_00757 | 1.4e-22 | |||||
NHEFJLLP_00758 | 0.0 | traA | L | MobA/MobL family | ||
NHEFJLLP_00759 | 1.7e-78 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
NHEFJLLP_00760 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
NHEFJLLP_00761 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_00762 | 3e-30 | |||||
NHEFJLLP_00763 | 1.4e-44 | yhdG | E | C-terminus of AA_permease | ||
NHEFJLLP_00764 | 1.4e-44 | yhdG | E | C-terminus of AA_permease | ||
NHEFJLLP_00765 | 0.0 | amiA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
NHEFJLLP_00766 | 5.9e-127 | amiC | U | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_00767 | 3.3e-122 | amiC | U | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_00768 | 5.3e-157 | amiD | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHEFJLLP_00769 | 3.1e-190 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHEFJLLP_00770 | 2.7e-142 | oppF | E | Oligopeptide/dipeptide transporter, C-terminal region | ||
NHEFJLLP_00771 | 3.1e-38 | drrA | V | ABC transporter | ||
NHEFJLLP_00772 | 5.6e-40 | drrA | V | ABC transporter | ||
NHEFJLLP_00773 | 2.3e-119 | lssY | 3.6.1.27 | I | phosphatase | |
NHEFJLLP_00774 | 2e-154 | I | alpha/beta hydrolase fold | |||
NHEFJLLP_00775 | 2.8e-99 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_00776 | 4.2e-92 | K | Transcriptional regulator | |||
NHEFJLLP_00777 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
NHEFJLLP_00778 | 7.4e-67 | gcvH | E | Glycine cleavage H-protein | ||
NHEFJLLP_00779 | 2.8e-176 | sepS16B | ||||
NHEFJLLP_00780 | 3.7e-131 | |||||
NHEFJLLP_00781 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
NHEFJLLP_00782 | 6.8e-57 | |||||
NHEFJLLP_00783 | 3.1e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NHEFJLLP_00784 | 8.7e-27 | 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 | ||
NHEFJLLP_00785 | 5.5e-13 | |||||
NHEFJLLP_00786 | 4.6e-45 | |||||
NHEFJLLP_00787 | 1.9e-98 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_00788 | 1.3e-109 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_00789 | 2.7e-153 | S | Cell surface protein | |||
NHEFJLLP_00790 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
NHEFJLLP_00791 | 8.4e-262 | nox | C | NADH oxidase | ||
NHEFJLLP_00792 | 2.1e-67 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
NHEFJLLP_00795 | 2.4e-29 | S | Domain of unknown function (DUF4440) | |||
NHEFJLLP_00796 | 4.9e-201 | ugpB | G | Bacterial extracellular solute-binding protein | ||
NHEFJLLP_00797 | 4.1e-124 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NHEFJLLP_00798 | 3.8e-119 | dck | 2.7.1.74 | F | deoxynucleoside kinase | |
NHEFJLLP_00799 | 5.5e-41 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
NHEFJLLP_00800 | 3.9e-179 | XK27_06930 | V | domain protein | ||
NHEFJLLP_00801 | 2.3e-31 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_00802 | 2.3e-31 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_00803 | 4.4e-20 | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | ||
NHEFJLLP_00804 | 0.0 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
NHEFJLLP_00805 | 8.4e-117 | cmpC | S | ATPases associated with a variety of cellular activities | ||
NHEFJLLP_00806 | 4.3e-154 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
NHEFJLLP_00807 | 3.5e-169 | XK27_00670 | S | ABC transporter | ||
NHEFJLLP_00808 | 9.3e-65 | |||||
NHEFJLLP_00809 | 1.5e-36 | |||||
NHEFJLLP_00810 | 4.6e-29 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
NHEFJLLP_00811 | 1.4e-19 | |||||
NHEFJLLP_00812 | 6.1e-220 | pts15C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_00813 | 5.2e-47 | pts15B | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_00814 | 1.4e-51 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
NHEFJLLP_00815 | 6.9e-62 | S | Domain of unknown function (DUF3284) | |||
NHEFJLLP_00816 | 0.0 | K | PRD domain | |||
NHEFJLLP_00817 | 9.9e-107 | |||||
NHEFJLLP_00818 | 4.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
NHEFJLLP_00819 | 2.9e-12 | |||||
NHEFJLLP_00820 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NHEFJLLP_00821 | 1e-54 | yheA | S | Belongs to the UPF0342 family | ||
NHEFJLLP_00822 | 5.7e-233 | yhaO | L | Ser Thr phosphatase family protein | ||
NHEFJLLP_00823 | 3.3e-103 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
NHEFJLLP_00824 | 6.8e-259 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
NHEFJLLP_00825 | 3.3e-132 | yliE | T | Putative diguanylate phosphodiesterase | ||
NHEFJLLP_00826 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
NHEFJLLP_00827 | 1.1e-61 | S | Protein of unknown function (DUF3290) | |||
NHEFJLLP_00828 | 2e-109 | yviA | S | Protein of unknown function (DUF421) | ||
NHEFJLLP_00829 | 1.8e-40 | M | Glycosyl transferase family group 2 | |||
NHEFJLLP_00830 | 4.2e-37 | M | Glycosyl transferase family group 2 | |||
NHEFJLLP_00831 | 1.1e-129 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_00832 | 1.1e-192 | yxaB | GM | Polysaccharide pyruvyl transferase | ||
NHEFJLLP_00833 | 9.7e-243 | iolT | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00834 | 7.8e-29 | ytgB | S | Transglycosylase associated protein | ||
NHEFJLLP_00835 | 7.5e-98 | tnpR | L | Resolvase, N terminal domain | ||
NHEFJLLP_00837 | 2.5e-236 | L | Transposase | |||
NHEFJLLP_00838 | 2.4e-19 | |||||
NHEFJLLP_00839 | 0.0 | O | Belongs to the peptidase S8 family | |||
NHEFJLLP_00840 | 0.0 | traA | L | MobA MobL family protein | ||
NHEFJLLP_00841 | 3.6e-26 | |||||
NHEFJLLP_00842 | 4e-41 | |||||
NHEFJLLP_00843 | 1e-27 | S | protein conserved in bacteria | |||
NHEFJLLP_00844 | 2.4e-59 | dprA | LU | DNA recombination-mediator protein A | ||
NHEFJLLP_00846 | 2e-191 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_00847 | 3.1e-54 | S | protein conserved in bacteria | |||
NHEFJLLP_00848 | 5.9e-28 | |||||
NHEFJLLP_00849 | 9.6e-43 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
NHEFJLLP_00850 | 1.7e-120 | repA | S | Replication initiator protein A | ||
NHEFJLLP_00851 | 3.6e-52 | darA | C | Flavodoxin | ||
NHEFJLLP_00852 | 2.1e-80 | GM | NmrA-like family | |||
NHEFJLLP_00853 | 3.1e-136 | C | Aldo/keto reductase family | |||
NHEFJLLP_00854 | 1.3e-150 | S | Hydrolases of the alpha beta superfamily | |||
NHEFJLLP_00855 | 9.3e-37 | fldA | C | Flavodoxin | ||
NHEFJLLP_00856 | 2.3e-47 | adhR | K | helix_turn_helix, mercury resistance | ||
NHEFJLLP_00857 | 3.8e-29 | |||||
NHEFJLLP_00858 | 2.1e-121 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
NHEFJLLP_00859 | 1.1e-46 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
NHEFJLLP_00860 | 5.6e-21 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
NHEFJLLP_00861 | 1.6e-18 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NHEFJLLP_00862 | 0.0 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
NHEFJLLP_00863 | 5.9e-115 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
NHEFJLLP_00864 | 9.7e-130 | S | haloacid dehalogenase-like hydrolase | |||
NHEFJLLP_00865 | 1e-47 | ysnF | S | Heat induced stress protein YflT | ||
NHEFJLLP_00866 | 5.2e-156 | L | PFAM Integrase, catalytic core | |||
NHEFJLLP_00867 | 1.9e-46 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
NHEFJLLP_00868 | 7.4e-52 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
NHEFJLLP_00869 | 4.9e-28 | M | Lysin motif | |||
NHEFJLLP_00870 | 1.3e-120 | S | CAAX protease self-immunity | |||
NHEFJLLP_00871 | 2.5e-114 | V | CAAX protease self-immunity | |||
NHEFJLLP_00872 | 7.1e-121 | yclH | V | ABC transporter | ||
NHEFJLLP_00873 | 1.7e-194 | yclI | V | MacB-like periplasmic core domain | ||
NHEFJLLP_00874 | 1e-159 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
NHEFJLLP_00875 | 6.9e-207 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
NHEFJLLP_00876 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
NHEFJLLP_00877 | 3.3e-118 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | ||
NHEFJLLP_00878 | 1.6e-32 | copZ | P | Heavy-metal-associated domain | ||
NHEFJLLP_00879 | 1.2e-94 | dps | P | Belongs to the Dps family | ||
NHEFJLLP_00880 | 1.2e-18 | |||||
NHEFJLLP_00881 | 5.6e-40 | yrkD | S | Metal-sensitive transcriptional repressor | ||
NHEFJLLP_00882 | 1.5e-55 | txlA | O | Thioredoxin-like domain | ||
NHEFJLLP_00883 | 1.7e-142 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_00884 | 1.9e-40 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
NHEFJLLP_00885 | 2.4e-30 | S | YheO-like PAS domain | |||
NHEFJLLP_00886 | 1.9e-30 | 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 | |
NHEFJLLP_00887 | 4.3e-118 | hisG | 2.4.2.17 | F | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
NHEFJLLP_00888 | 7.8e-233 | 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 | |
NHEFJLLP_00889 | 2.3e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
NHEFJLLP_00890 | 1.2e-109 | 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 | ||
NHEFJLLP_00891 | 3.5e-129 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
NHEFJLLP_00892 | 7.6e-135 | 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 | |
NHEFJLLP_00893 | 3.8e-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 | |
NHEFJLLP_00894 | 7.6e-52 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
NHEFJLLP_00895 | 3.3e-36 | hsp3 | O | Belongs to the small heat shock protein (HSP20) family | ||
NHEFJLLP_00896 | 3.3e-36 | hsp3 | O | Belongs to the small heat shock protein (HSP20) family | ||
NHEFJLLP_00897 | 2.8e-41 | 4.1.1.52 | S | Amidohydrolase | ||
NHEFJLLP_00898 | 5.4e-36 | 4.1.1.52 | S | Amidohydrolase | ||
NHEFJLLP_00899 | 1e-09 | |||||
NHEFJLLP_00900 | 6.2e-114 | 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) | |
NHEFJLLP_00901 | 1.8e-125 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
NHEFJLLP_00902 | 2.2e-168 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
NHEFJLLP_00903 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
NHEFJLLP_00904 | 6.2e-75 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
NHEFJLLP_00905 | 1.2e-187 | yueF | S | AI-2E family transporter | ||
NHEFJLLP_00906 | 3.7e-72 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
NHEFJLLP_00907 | 9.5e-213 | gntP | EG | Gluconate | ||
NHEFJLLP_00908 | 4.6e-293 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17, 2.7.1.5 | G | Belongs to the FGGY kinase family | |
NHEFJLLP_00909 | 1.7e-170 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
NHEFJLLP_00910 | 8.5e-293 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
NHEFJLLP_00911 | 1e-31 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
NHEFJLLP_00912 | 6.1e-109 | ydiL | S | CAAX protease self-immunity | ||
NHEFJLLP_00913 | 1.4e-119 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
NHEFJLLP_00914 | 1.1e-307 | uup | S | ABC transporter, ATP-binding protein | ||
NHEFJLLP_00915 | 1.7e-177 | EG | EamA-like transporter family | |||
NHEFJLLP_00916 | 3.3e-167 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
NHEFJLLP_00917 | 4.8e-168 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NHEFJLLP_00918 | 1.8e-136 | accA | 2.1.3.15, 6.4.1.2 | I | Acetyl co-enzyme A carboxylase carboxyltransferase alpha subunit | |
NHEFJLLP_00919 | 2.2e-140 | 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 | |
NHEFJLLP_00920 | 1.1e-33 | ydgH | S | MMPL family | ||
NHEFJLLP_00921 | 1.3e-26 | ydgH | S | MMPL family | ||
NHEFJLLP_00922 | 2.3e-100 | |||||
NHEFJLLP_00923 | 8.9e-23 | L | hmm pf00665 | |||
NHEFJLLP_00924 | 6.9e-29 | L | hmm pf00665 | |||
NHEFJLLP_00925 | 2e-18 | L | hmm pf00665 | |||
NHEFJLLP_00926 | 7.6e-46 | L | Helix-turn-helix domain | |||
NHEFJLLP_00928 | 6.6e-143 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
NHEFJLLP_00929 | 1.9e-43 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NHEFJLLP_00930 | 1e-41 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NHEFJLLP_00931 | 7.4e-194 | C | Aldo keto reductase family protein | |||
NHEFJLLP_00932 | 1.1e-173 | galR | K | Transcriptional regulator | ||
NHEFJLLP_00933 | 4.5e-199 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
NHEFJLLP_00934 | 0.0 | lacS | G | Transporter | ||
NHEFJLLP_00935 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
NHEFJLLP_00936 | 1.4e-186 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
NHEFJLLP_00937 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
NHEFJLLP_00938 | 9.3e-225 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
NHEFJLLP_00939 | 8.9e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NHEFJLLP_00940 | 5e-284 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
NHEFJLLP_00941 | 2e-183 | galR | K | Transcriptional regulator | ||
NHEFJLLP_00942 | 1.6e-76 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_00943 | 3.5e-111 | fic | D | Fic/DOC family | ||
NHEFJLLP_00944 | 7.4e-183 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
NHEFJLLP_00945 | 1.2e-230 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_00946 | 7.9e-304 | ram2 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | |
NHEFJLLP_00947 | 4.6e-28 | |||||
NHEFJLLP_00948 | 1.7e-60 | |||||
NHEFJLLP_00949 | 7e-64 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_00950 | 4.8e-105 | L | Integrase | |||
NHEFJLLP_00951 | 1.4e-40 | K | prlF antitoxin for toxin YhaV_toxin | |||
NHEFJLLP_00952 | 1.4e-56 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
NHEFJLLP_00953 | 4.3e-87 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain protein | ||
NHEFJLLP_00954 | 1.3e-94 | |||||
NHEFJLLP_00955 | 7.3e-172 | L | Initiator Replication protein | |||
NHEFJLLP_00956 | 1.4e-23 | |||||
NHEFJLLP_00957 | 1.2e-210 | phnW | 2.5.1.49, 2.6.1.37, 3.11.1.1 | E | Belongs to the class-V pyridoxal-phosphate-dependent aminotransferase family. PhnW subfamily | |
NHEFJLLP_00958 | 4.2e-144 | phnX | 2.6.1.37, 3.1.3.18, 3.11.1.1 | E | Belongs to the HAD-like hydrolase superfamily. PhnX family | |
NHEFJLLP_00959 | 2.6e-144 | phnE1 | 3.6.1.63 | U | ABC transporter permease | |
NHEFJLLP_00960 | 7.7e-138 | phnE | 3.6.1.63 | U | Phosphonate ABC transporter permease | |
NHEFJLLP_00961 | 9.7e-138 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
NHEFJLLP_00962 | 3.8e-137 | phnD | P | Phosphonate ABC transporter | ||
NHEFJLLP_00963 | 9.5e-44 | phnD | P | Phosphonate ABC transporter | ||
NHEFJLLP_00964 | 6.1e-271 | G | Major Facilitator | |||
NHEFJLLP_00965 | 1.1e-173 | K | Transcriptional regulator, LacI family | |||
NHEFJLLP_00966 | 5.6e-266 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
NHEFJLLP_00967 | 2e-160 | I | alpha/beta hydrolase fold | |||
NHEFJLLP_00968 | 4.8e-131 | treR | K | UTRA | ||
NHEFJLLP_00969 | 2.9e-167 | |||||
NHEFJLLP_00970 | 3.1e-41 | norA | EGP | Major facilitator Superfamily | ||
NHEFJLLP_00971 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
NHEFJLLP_00972 | 1.5e-180 | 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 | |
NHEFJLLP_00973 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NHEFJLLP_00974 | 5.9e-34 | pva1 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
NHEFJLLP_00975 | 7.4e-250 | yjjP | S | Putative threonine/serine exporter | ||
NHEFJLLP_00976 | 5.7e-135 | wzb | 3.1.3.48 | T | Tyrosine phosphatase family | |
NHEFJLLP_00977 | 2.4e-254 | 1.14.14.9 | Q | 4-hydroxyphenylacetate | ||
NHEFJLLP_00978 | 2.9e-81 | 6.3.3.2 | S | ASCH | ||
NHEFJLLP_00979 | 1.4e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
NHEFJLLP_00980 | 8.7e-104 | yobV1 | K | WYL domain | ||
NHEFJLLP_00981 | 6e-36 | |||||
NHEFJLLP_00982 | 1.4e-134 | levD | G | PTS system mannose/fructose/sorbose family IID component | ||
NHEFJLLP_00983 | 5.3e-137 | M | PTS system sorbose-specific iic component | |||
NHEFJLLP_00984 | 6.6e-79 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
NHEFJLLP_00985 | 9.6e-42 | levA | G | PTS system fructose IIA component | ||
NHEFJLLP_00986 | 1.9e-299 | K | Sigma-54 interaction domain | |||
NHEFJLLP_00987 | 3.9e-44 | tesE | Q | hydratase | ||
NHEFJLLP_00988 | 2e-45 | tesE | Q | hydratase | ||
NHEFJLLP_00989 | 7.4e-40 | |||||
NHEFJLLP_00990 | 2.1e-39 | |||||
NHEFJLLP_00991 | 1.1e-26 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NHEFJLLP_00992 | 2.3e-311 | oppA | E | ABC transporter, substratebinding protein | ||
NHEFJLLP_00993 | 2.3e-165 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHEFJLLP_00994 | 1.1e-189 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NHEFJLLP_00995 | 3.5e-202 | oppD | P | Belongs to the ABC transporter superfamily | ||
NHEFJLLP_00996 | 1.8e-181 | oppF | P | Belongs to the ABC transporter superfamily | ||
NHEFJLLP_00997 | 2.9e-31 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
NHEFJLLP_00998 | 7.7e-32 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
NHEFJLLP_00999 | 3.8e-41 | |||||
NHEFJLLP_01000 | 7e-37 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
NHEFJLLP_01001 | 2.8e-122 | mngA | 2.7.1.195, 2.7.1.202 | U | Phosphotransferase system, EIIC | |
NHEFJLLP_01002 | 2.4e-26 | mngA | 2.7.1.195, 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_01003 | 1.7e-20 | fryA | 2.7.1.202 | G | COG1762 Phosphotransferase system mannitol fructose-specific IIA domain (Ntr-type) | |
NHEFJLLP_01004 | 2.2e-90 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHEFJLLP_01005 | 3.6e-225 | XK27_09615 | 1.3.5.4 | S | reductase | |
NHEFJLLP_01006 | 1.8e-110 | XK27_09620 | 1.3.5.4 | S | NADPH-dependent FMN reductase | |
NHEFJLLP_01007 | 4.9e-190 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
NHEFJLLP_01008 | 1.2e-146 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
NHEFJLLP_01009 | 1.9e-118 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
NHEFJLLP_01010 | 8.3e-148 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_01011 | 9.5e-220 | ydiN | 5.4.99.5 | G | Major Facilitator | |
NHEFJLLP_01012 | 1e-215 | 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 | |
NHEFJLLP_01013 | 8.5e-93 | |||||
NHEFJLLP_01014 | 3e-232 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
NHEFJLLP_01015 | 1.9e-195 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
NHEFJLLP_01016 | 2e-86 | 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 | |
NHEFJLLP_01017 | 3.6e-171 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
NHEFJLLP_01018 | 2.7e-188 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
NHEFJLLP_01019 | 7.3e-132 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
NHEFJLLP_01020 | 2.4e-195 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
NHEFJLLP_01021 | 1.5e-80 | 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 | ||
NHEFJLLP_01022 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
NHEFJLLP_01023 | 4.6e-184 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
NHEFJLLP_01024 | 4.4e-198 | pbpX2 | V | Beta-lactamase | ||
NHEFJLLP_01025 | 8.8e-19 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
NHEFJLLP_01026 | 7e-297 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
NHEFJLLP_01027 | 8.7e-234 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
NHEFJLLP_01028 | 2.4e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
NHEFJLLP_01029 | 6.1e-246 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
NHEFJLLP_01030 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
NHEFJLLP_01031 | 7.9e-305 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
NHEFJLLP_01032 | 4.2e-175 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain | |
NHEFJLLP_01033 | 7.4e-112 | cysC | 2.7.1.25, 2.7.7.4 | F | Catalyzes the synthesis of activated sulfate | |
NHEFJLLP_01034 | 1.8e-155 | sat | 2.7.7.4 | H | the enzyme from Thermus thermophilus is dimeric and binds a zinc ion that is coordinated by cysteine and histidine residues that are not found in all related proteins but is found in some thermophilic organisms | |
NHEFJLLP_01035 | 0.0 | levR | K | Sigma-54 interaction domain | ||
NHEFJLLP_01036 | 8.6e-72 | pts10A | 2.7.1.191 | G | PTS system fructose IIA component | |
NHEFJLLP_01037 | 3.1e-87 | pts10B | 2.7.1.191, 2.7.1.202 | G | PTS system sorbose subfamily IIB component | |
NHEFJLLP_01038 | 5.4e-178 | 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 | |
NHEFJLLP_01039 | 9.7e-65 | accB | 2.3.1.12 | I | Biotin-requiring enzyme | |
NHEFJLLP_01040 | 1.1e-135 | D | Cellulose biosynthesis protein BcsQ | |||
NHEFJLLP_01042 | 4.3e-119 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_01043 | 1.5e-17 | |||||
NHEFJLLP_01044 | 2.2e-24 | KLT | serine threonine protein kinase | |||
NHEFJLLP_01045 | 1.4e-107 | U | TraM recognition site of TraD and TraG | |||
NHEFJLLP_01046 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
NHEFJLLP_01047 | 7.6e-117 | 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 | ||
NHEFJLLP_01048 | 8.3e-110 | ypsA | S | Belongs to the UPF0398 family | ||
NHEFJLLP_01049 | 2e-62 | 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 | ||
NHEFJLLP_01051 | 1.5e-115 | GM | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_01052 | 5.9e-91 | rmeB | K | transcriptional regulator, MerR family | ||
NHEFJLLP_01053 | 2.1e-55 | S | Domain of unknown function (DU1801) | |||
NHEFJLLP_01054 | 7.6e-166 | corA | P | CorA-like Mg2+ transporter protein | ||
NHEFJLLP_01055 | 4.6e-216 | ysaA | V | RDD family | ||
NHEFJLLP_01056 | 1.7e-164 | hisK | 3.1.3.15 | E | Histidinol phosphate phosphatase, HisJ | |
NHEFJLLP_01058 | 4.6e-57 | |||||
NHEFJLLP_01059 | 3.5e-10 | |||||
NHEFJLLP_01060 | 7.9e-180 | |||||
NHEFJLLP_01061 | 1.9e-89 | gtcA | S | Teichoic acid glycosylation protein | ||
NHEFJLLP_01062 | 3.6e-58 | S | Protein of unknown function (DUF1516) | |||
NHEFJLLP_01063 | 0.0 | yitJ | 1.5.1.20, 2.1.1.10, 2.1.1.13 | E | catalyzes the formation of 5,10-methylenetetrahydrofolate from 5-methyltetrahydrofolate and S-adenosyl-L-homocysteine and methionine from S-adenosyl-L-methionine and L-homocysteine | |
NHEFJLLP_01064 | 3.1e-150 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
NHEFJLLP_01065 | 3.2e-100 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
NHEFJLLP_01066 | 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) | |
NHEFJLLP_01067 | 2.4e-242 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NHEFJLLP_01068 | 1.9e-155 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
NHEFJLLP_01069 | 2e-180 | ydaO | E | amino acid | ||
NHEFJLLP_01070 | 3.5e-181 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
NHEFJLLP_01071 | 2.8e-144 | pstS | P | Phosphate | ||
NHEFJLLP_01072 | 1.7e-114 | yvyE | 3.4.13.9 | S | YigZ family | |
NHEFJLLP_01073 | 7.4e-258 | comFA | L | Helicase C-terminal domain protein | ||
NHEFJLLP_01074 | 3.7e-231 | pts3C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_01075 | 4.7e-39 | |||||
NHEFJLLP_01076 | 4.6e-210 | S | Bacterial protein of unknown function (DUF871) | |||
NHEFJLLP_01077 | 4.7e-210 | dho | 3.5.2.3 | S | Amidohydrolase family | |
NHEFJLLP_01078 | 2.3e-201 | selA | 2.9.1.1 | H | L-seryl-tRNA selenium transferase | |
NHEFJLLP_01079 | 2.5e-88 | |||||
NHEFJLLP_01080 | 1.9e-147 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
NHEFJLLP_01081 | 3.9e-72 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
NHEFJLLP_01082 | 1.8e-19 | |||||
NHEFJLLP_01083 | 3.1e-104 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
NHEFJLLP_01084 | 1.3e-81 | zur | P | Belongs to the Fur family | ||
NHEFJLLP_01085 | 7.1e-12 | 3.2.1.14 | GH18 | |||
NHEFJLLP_01086 | 4.4e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NHEFJLLP_01087 | 2.1e-102 | J | Acetyltransferase (GNAT) domain | |||
NHEFJLLP_01088 | 2.7e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
NHEFJLLP_01089 | 2.3e-43 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
NHEFJLLP_01090 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
NHEFJLLP_01091 | 9.3e-220 | rodA | D | Belongs to the SEDS family | ||
NHEFJLLP_01092 | 3.6e-48 | gcsH2 | E | glycine cleavage | ||
NHEFJLLP_01093 | 4e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NHEFJLLP_01094 | 1.4e-111 | metI | U | ABC transporter permease | ||
NHEFJLLP_01095 | 2.2e-148 | metQ | M | Belongs to the nlpA lipoprotein family | ||
NHEFJLLP_01096 | 8.2e-168 | hicD1 | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
NHEFJLLP_01097 | 1.6e-177 | S | Protein of unknown function (DUF2785) | |||
NHEFJLLP_01098 | 1e-187 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
NHEFJLLP_01099 | 1.6e-213 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
NHEFJLLP_01100 | 1.3e-295 | glpQ3 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
NHEFJLLP_01101 | 3.3e-161 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
NHEFJLLP_01102 | 3.1e-201 | bla2 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
NHEFJLLP_01103 | 6.2e-82 | usp6 | T | universal stress protein | ||
NHEFJLLP_01104 | 1.5e-38 | |||||
NHEFJLLP_01105 | 8e-238 | rarA | L | recombination factor protein RarA | ||
NHEFJLLP_01106 | 2e-39 | S | Peptidase propeptide and YPEB domain | |||
NHEFJLLP_01107 | 7e-170 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
NHEFJLLP_01108 | 1e-273 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
NHEFJLLP_01109 | 4.2e-245 | rarA | L | recombination factor protein RarA | ||
NHEFJLLP_01110 | 4.3e-121 | K | response regulator | |||
NHEFJLLP_01111 | 9.4e-225 | lsgC | M | Glycosyl transferases group 1 | ||
NHEFJLLP_01112 | 5.6e-21 | S | Protein of unknown function (DUF2929) | |||
NHEFJLLP_01113 | 1.7e-48 | K | Cro/C1-type HTH DNA-binding domain | |||
NHEFJLLP_01114 | 3.7e-69 | S | response to antibiotic | |||
NHEFJLLP_01115 | 4.2e-44 | S | zinc-ribbon domain | |||
NHEFJLLP_01116 | 6.6e-159 | traI | 5.99.1.2 | L | C-terminal repeat of topoisomerase | |
NHEFJLLP_01120 | 6.4e-99 | M | Glycosyl hydrolases family 25 | |||
NHEFJLLP_01121 | 1.2e-15 | K | Helix-turn-helix domain | |||
NHEFJLLP_01123 | 1.1e-48 | L | hmm pf00665 | |||
NHEFJLLP_01124 | 6e-58 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
NHEFJLLP_01125 | 1.7e-44 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
NHEFJLLP_01126 | 1.6e-25 | L | Integrase | |||
NHEFJLLP_01127 | 2.7e-61 | L | Integrase | |||
NHEFJLLP_01128 | 6e-49 | |||||
NHEFJLLP_01130 | 8.1e-15 | |||||
NHEFJLLP_01131 | 2.1e-160 | yceM | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, NAD-binding Rossmann fold | |
NHEFJLLP_01132 | 6.2e-168 | murB | 1.3.1.98 | M | Cell wall formation | |
NHEFJLLP_01133 | 0.0 | yjcE | P | Sodium proton antiporter | ||
NHEFJLLP_01134 | 1.3e-90 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_01135 | 1.8e-107 | S | Protein of unknown function (DUF1361) | |||
NHEFJLLP_01136 | 2.2e-76 | S | Threonine/Serine exporter, ThrE | |||
NHEFJLLP_01137 | 1.5e-130 | thrE | S | Putative threonine/serine exporter | ||
NHEFJLLP_01138 | 6e-31 | cspC | K | Cold shock protein | ||
NHEFJLLP_01139 | 2e-120 | sirR | K | iron dependent repressor | ||
NHEFJLLP_01140 | 2.6e-58 | |||||
NHEFJLLP_01141 | 1.7e-84 | merR | K | MerR HTH family regulatory protein | ||
NHEFJLLP_01142 | 1.2e-42 | lmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_01143 | 6.1e-58 | lmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_01144 | 6.6e-90 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NHEFJLLP_01145 | 3e-18 | |||||
NHEFJLLP_01146 | 1.7e-126 | S | membrane transporter protein | |||
NHEFJLLP_01147 | 3.6e-160 | mleR | K | LysR family | ||
NHEFJLLP_01148 | 5.6e-115 | ylbE | GM | NAD(P)H-binding | ||
NHEFJLLP_01149 | 8.2e-96 | wecD | K | Acetyltransferase (GNAT) family | ||
NHEFJLLP_01150 | 5.6e-250 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
NHEFJLLP_01151 | 1.6e-263 | ycaM | E | amino acid | ||
NHEFJLLP_01152 | 3.1e-128 | aroD | 1.1.1.25, 4.2.1.10 | E | Type I 3-dehydroquinase | |
NHEFJLLP_01153 | 2.7e-32 | |||||
NHEFJLLP_01154 | 1.6e-188 | lacR | K | Transcriptional regulator | ||
NHEFJLLP_01155 | 0.0 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
NHEFJLLP_01156 | 0.0 | lacS | G | Transporter | ||
NHEFJLLP_01157 | 8.2e-28 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
NHEFJLLP_01158 | 6e-97 | S | Domain of unknown function (DUF4352) | |||
NHEFJLLP_01159 | 2.9e-23 | S | Protein of unknown function (DUF4064) | |||
NHEFJLLP_01160 | 2.9e-201 | KLT | Protein tyrosine kinase | |||
NHEFJLLP_01161 | 3.6e-163 | |||||
NHEFJLLP_01162 | 4.7e-232 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
NHEFJLLP_01164 | 2.2e-41 | K | HxlR-like helix-turn-helix | |||
NHEFJLLP_01166 | 2.3e-21 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
NHEFJLLP_01167 | 1.5e-11 | |||||
NHEFJLLP_01168 | 9.2e-65 | |||||
NHEFJLLP_01169 | 1.6e-247 | celD | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_01170 | 9.9e-269 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_01171 | 2.2e-115 | K | UTRA | |||
NHEFJLLP_01172 | 1.7e-84 | dps | P | Belongs to the Dps family | ||
NHEFJLLP_01173 | 0.0 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | S | MucBP domain | |
NHEFJLLP_01174 | 5.2e-281 | 1.3.5.4 | C | FAD binding domain | ||
NHEFJLLP_01175 | 1.6e-160 | K | LysR substrate binding domain | |||
NHEFJLLP_01176 | 1.5e-152 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
NHEFJLLP_01177 | 1.3e-290 | yjcE | P | Sodium proton antiporter | ||
NHEFJLLP_01178 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
NHEFJLLP_01179 | 1.4e-116 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01180 | 1.2e-188 | NU | Mycoplasma protein of unknown function, DUF285 | |||
NHEFJLLP_01181 | 8.7e-83 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_01182 | 8.5e-169 | S | Bacterial protein of unknown function (DUF916) | |||
NHEFJLLP_01183 | 0.0 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
NHEFJLLP_01184 | 5.6e-165 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
NHEFJLLP_01185 | 8.6e-63 | K | helix_turn_helix, mercury resistance | |||
NHEFJLLP_01186 | 7e-150 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHEFJLLP_01187 | 4.8e-68 | maa | S | transferase hexapeptide repeat | ||
NHEFJLLP_01188 | 2.5e-130 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_01189 | 2e-163 | GM | NmrA-like family | |||
NHEFJLLP_01190 | 5.4e-92 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01191 | 7.8e-172 | fhuG | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHEFJLLP_01192 | 1.4e-176 | sirB | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NHEFJLLP_01193 | 7.2e-144 | fhuC | 3.6.3.34 | HP | ABC transporter | |
NHEFJLLP_01194 | 4e-170 | fhuD | P | Periplasmic binding protein | ||
NHEFJLLP_01195 | 4.3e-109 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01196 | 1.6e-253 | yfjF | U | Sugar (and other) transporter | ||
NHEFJLLP_01199 | 1.5e-180 | S | Aldo keto reductase | |||
NHEFJLLP_01200 | 4.1e-101 | S | Protein of unknown function (DUF1211) | |||
NHEFJLLP_01201 | 1.2e-191 | 1.1.1.219 | GM | Male sterility protein | ||
NHEFJLLP_01202 | 3.2e-98 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01203 | 9.8e-132 | ydfG | S | KR domain | ||
NHEFJLLP_01204 | 8.3e-63 | hxlR | K | HxlR-like helix-turn-helix | ||
NHEFJLLP_01205 | 8.5e-47 | S | Domain of unknown function (DUF1905) | |||
NHEFJLLP_01206 | 0.0 | M | Glycosyl hydrolases family 25 | |||
NHEFJLLP_01207 | 2.6e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
NHEFJLLP_01208 | 4.4e-112 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
NHEFJLLP_01209 | 5.5e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
NHEFJLLP_01210 | 1.8e-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 | ||
NHEFJLLP_01211 | 8.1e-146 | 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 | ||
NHEFJLLP_01212 | 8.2e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
NHEFJLLP_01213 | 2.8e-52 | 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 | ||
NHEFJLLP_01214 | 2.1e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
NHEFJLLP_01215 | 9.2e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
NHEFJLLP_01216 | 1.4e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
NHEFJLLP_01217 | 2.5e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
NHEFJLLP_01218 | 4.3e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
NHEFJLLP_01219 | 2.4e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
NHEFJLLP_01220 | 3.2e-95 | 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 | ||
NHEFJLLP_01221 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
NHEFJLLP_01222 | 3.5e-94 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
NHEFJLLP_01223 | 3.3e-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 | ||
NHEFJLLP_01224 | 6.8e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
NHEFJLLP_01225 | 2.2e-24 | rpmD | J | Ribosomal protein L30 | ||
NHEFJLLP_01226 | 6.3e-70 | rplO | J | Binds to the 23S rRNA | ||
NHEFJLLP_01227 | 1.5e-236 | 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 | ||
NHEFJLLP_01228 | 2.1e-125 | 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 | |
NHEFJLLP_01229 | 4.1e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
NHEFJLLP_01230 | 1.1e-59 | 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 | ||
NHEFJLLP_01231 | 3.4e-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 | ||
NHEFJLLP_01232 | 5.7e-172 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NHEFJLLP_01233 | 2.1e-61 | rplQ | J | Ribosomal protein L17 | ||
NHEFJLLP_01234 | 1.1e-180 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NHEFJLLP_01235 | 1.4e-86 | ynhH | S | NusG domain II | ||
NHEFJLLP_01236 | 0.0 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
NHEFJLLP_01237 | 3.5e-142 | cad | S | FMN_bind | ||
NHEFJLLP_01238 | 1.5e-208 | 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 | |
NHEFJLLP_01246 | 5.5e-08 | |||||
NHEFJLLP_01256 | 1.3e-90 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
NHEFJLLP_01257 | 1.1e-138 | yhfI | S | Metallo-beta-lactamase superfamily | ||
NHEFJLLP_01258 | 2.7e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
NHEFJLLP_01259 | 2.2e-131 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
NHEFJLLP_01260 | 1.5e-37 | XK26_04895 | ||||
NHEFJLLP_01261 | 1.1e-48 | 3.4.21.19 | M | Belongs to the peptidase S1B family | ||
NHEFJLLP_01262 | 6.2e-44 | S | Psort location CytoplasmicMembrane, score | |||
NHEFJLLP_01264 | 1.6e-29 | |||||
NHEFJLLP_01265 | 2e-19 | M | Lysin motif | |||
NHEFJLLP_01266 | 3.8e-117 | 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 | |
NHEFJLLP_01267 | 1.8e-213 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
NHEFJLLP_01268 | 2.7e-249 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
NHEFJLLP_01269 | 1.1e-40 | 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 | ||
NHEFJLLP_01270 | 1.5e-95 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01271 | 1.2e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
NHEFJLLP_01272 | 6.8e-173 | htrA | 3.4.21.107 | O | serine protease | |
NHEFJLLP_01273 | 8.9e-158 | vicX | 3.1.26.11 | S | domain protein | |
NHEFJLLP_01276 | 4.8e-25 | I | mechanosensitive ion channel activity | |||
NHEFJLLP_01278 | 3.3e-15 | |||||
NHEFJLLP_01280 | 2.2e-99 | sigH | K | Sigma-70 region 2 | ||
NHEFJLLP_01281 | 6.5e-22 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NHEFJLLP_01282 | 6.8e-29 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
NHEFJLLP_01283 | 3.7e-99 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
NHEFJLLP_01284 | 1.7e-157 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_01285 | 2.4e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NHEFJLLP_01286 | 5.1e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
NHEFJLLP_01287 | 4.6e-80 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
NHEFJLLP_01288 | 3.2e-57 | ywjH | S | Protein of unknown function (DUF1634) | ||
NHEFJLLP_01289 | 5.5e-126 | yxaA | S | membrane transporter protein | ||
NHEFJLLP_01290 | 7.1e-161 | lysR5 | K | LysR substrate binding domain | ||
NHEFJLLP_01291 | 6.5e-198 | M | MucBP domain | |||
NHEFJLLP_01292 | 5.9e-274 | |||||
NHEFJLLP_01293 | 4.4e-112 | 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 | |
NHEFJLLP_01294 | 2e-230 | 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 | |
NHEFJLLP_01295 | 9.4e-130 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
NHEFJLLP_01296 | 9.3e-217 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
NHEFJLLP_01297 | 9.4e-189 | 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 | |
NHEFJLLP_01298 | 3.2e-240 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
NHEFJLLP_01299 | 2.2e-45 | ulaB | 2.7.1.194, 2.7.1.200 | G | Phosphotransferase system galactitol-specific IIB component | |
NHEFJLLP_01300 | 6.7e-78 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHEFJLLP_01301 | 0.0 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHEFJLLP_01302 | 1.8e-113 | gph | 3.1.3.18 | S | Haloacid dehalogenase-like hydrolase | |
NHEFJLLP_01303 | 8.9e-101 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
NHEFJLLP_01304 | 2.5e-32 | rmeB | K | transcriptional regulator, MerR family | ||
NHEFJLLP_01305 | 7.8e-71 | S | Thymidylate synthase | |||
NHEFJLLP_01306 | 6.3e-40 | S | Alpha beta hydrolase | |||
NHEFJLLP_01307 | 4.8e-51 | K | HTH domain | |||
NHEFJLLP_01308 | 2.9e-223 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
NHEFJLLP_01309 | 4.5e-171 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
NHEFJLLP_01310 | 1.5e-127 | C | Enoyl-(Acyl carrier protein) reductase | |||
NHEFJLLP_01311 | 2.1e-151 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
NHEFJLLP_01312 | 9.7e-23 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
NHEFJLLP_01313 | 2.6e-71 | yqeY | S | YqeY-like protein | ||
NHEFJLLP_01314 | 3.4e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
NHEFJLLP_01315 | 6.6e-84 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
NHEFJLLP_01316 | 4.5e-73 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
NHEFJLLP_01317 | 1.5e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
NHEFJLLP_01318 | 1.5e-146 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
NHEFJLLP_01319 | 6.8e-175 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
NHEFJLLP_01320 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
NHEFJLLP_01321 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
NHEFJLLP_01322 | 4.6e-197 | 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 | ||
NHEFJLLP_01323 | 9.5e-65 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
NHEFJLLP_01324 | 1.4e-164 | ytrB | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_01325 | 1.7e-201 | |||||
NHEFJLLP_01326 | 1.8e-113 | |||||
NHEFJLLP_01327 | 1.9e-71 | |||||
NHEFJLLP_01328 | 2.6e-127 | S | ABC-2 family transporter protein | |||
NHEFJLLP_01329 | 6.9e-116 | V | ABC transporter, ATP-binding protein | |||
NHEFJLLP_01330 | 4.6e-95 | cytR | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | |
NHEFJLLP_01331 | 6e-66 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
NHEFJLLP_01332 | 3.6e-103 | G | PTS system sorbose-specific iic component | |||
NHEFJLLP_01333 | 2.7e-104 | G | PTS system mannose fructose sorbose family IID component | |||
NHEFJLLP_01334 | 2.7e-41 | 2.7.1.191 | G | PTS system fructose IIA component | ||
NHEFJLLP_01335 | 9.4e-269 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
NHEFJLLP_01336 | 1.2e-149 | yitU | 3.1.3.104 | S | hydrolase | |
NHEFJLLP_01337 | 1.4e-265 | yfnA | E | Amino Acid | ||
NHEFJLLP_01338 | 1.7e-226 | gabT | 2.6.1.19, 5.1.1.21 | E | Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family | |
NHEFJLLP_01339 | 6.4e-238 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NHEFJLLP_01340 | 4.8e-213 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_01341 | 3.2e-124 | K | response regulator | |||
NHEFJLLP_01342 | 5.5e-124 | yoaK | S | Protein of unknown function (DUF1275) | ||
NHEFJLLP_01343 | 6.6e-295 | clcA | P | chloride | ||
NHEFJLLP_01344 | 1.2e-30 | secG | U | Preprotein translocase | ||
NHEFJLLP_01345 | 1.3e-139 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
NHEFJLLP_01348 | 6.2e-131 | K | response regulator | |||
NHEFJLLP_01349 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_01350 | 1.2e-244 | yycH | S | YycH protein | ||
NHEFJLLP_01351 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
NHEFJLLP_01352 | 1.6e-205 | ftsW | D | Belongs to the SEDS family | ||
NHEFJLLP_01353 | 6.4e-79 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
NHEFJLLP_01354 | 1.7e-120 | comEA | L | Competence protein ComEA | ||
NHEFJLLP_01355 | 1.1e-195 | ylbL | T | Belongs to the peptidase S16 family | ||
NHEFJLLP_01356 | 2.1e-85 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NHEFJLLP_01357 | 8.2e-102 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
NHEFJLLP_01358 | 8.5e-79 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
NHEFJLLP_01359 | 1.1e-31 | comEA | L | Competence protein ComEA | ||
NHEFJLLP_01360 | 1.9e-65 | comEA | L | Competence protein ComEA | ||
NHEFJLLP_01361 | 1.9e-189 | ylbL | T | Belongs to the peptidase S16 family | ||
NHEFJLLP_01362 | 3.7e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NHEFJLLP_01363 | 3.4e-100 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
NHEFJLLP_01364 | 4.9e-72 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
NHEFJLLP_01365 | 1.3e-237 | tagF1 | 2.7.8.12, 2.7.8.45 | M | glycerophosphotransferase | |
NHEFJLLP_01366 | 0.0 | tagF2 | 2.7.8.12 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
NHEFJLLP_01367 | 2.1e-237 | manR | K | PRD domain | ||
NHEFJLLP_01369 | 9.1e-75 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHEFJLLP_01370 | 8.6e-48 | fruA | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_01371 | 6.6e-172 | G | Phosphotransferase System | |||
NHEFJLLP_01372 | 4.5e-126 | alsE | 5.1.3.1 | G | Ribulose-phosphate 3 epimerase family | |
NHEFJLLP_01373 | 4.6e-255 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
NHEFJLLP_01374 | 2.1e-129 | jag | S | R3H domain protein | ||
NHEFJLLP_01375 | 3e-237 | Q | Imidazolonepropionase and related amidohydrolases | |||
NHEFJLLP_01376 | 2e-310 | E | ABC transporter, substratebinding protein | |||
NHEFJLLP_01377 | 1.8e-105 | 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 | ||
NHEFJLLP_01378 | 6.4e-57 | 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 | |
NHEFJLLP_01379 | 4.5e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
NHEFJLLP_01380 | 9.1e-256 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
NHEFJLLP_01381 | 1e-207 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
NHEFJLLP_01382 | 5e-37 | yaaA | S | S4 domain protein YaaA | ||
NHEFJLLP_01383 | 1.9e-206 | 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 | ||
NHEFJLLP_01384 | 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 | |
NHEFJLLP_01385 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
NHEFJLLP_01386 | 1.5e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
NHEFJLLP_01387 | 5.4e-66 | K | Winged helix DNA-binding domain | |||
NHEFJLLP_01388 | 7e-71 | spx4 | 1.20.4.1 | P | ArsC family | |
NHEFJLLP_01389 | 6.3e-66 | yeaO | S | Protein of unknown function, DUF488 | ||
NHEFJLLP_01390 | 4e-53 | |||||
NHEFJLLP_01391 | 4.1e-214 | mutY | L | A G-specific adenine glycosylase | ||
NHEFJLLP_01392 | 1.9e-62 | |||||
NHEFJLLP_01393 | 4.3e-86 | |||||
NHEFJLLP_01394 | 1.7e-129 | S | membrane | |||
NHEFJLLP_01395 | 1.2e-14 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01397 | 1e-70 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_01398 | 4.7e-28 | celB | 2.7.1.207 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
NHEFJLLP_01399 | 2.2e-97 | pre | D | Plasmid recombination enzyme | ||
NHEFJLLP_01400 | 2.1e-19 | |||||
NHEFJLLP_01401 | 4.4e-07 | S | Enterocin A Immunity | |||
NHEFJLLP_01402 | 1e-78 | S | Initiator Replication protein | |||
NHEFJLLP_01403 | 6.5e-09 | |||||
NHEFJLLP_01404 | 2.8e-144 | rgpAc | GT4 | M | Domain of unknown function (DUF1972) | |
NHEFJLLP_01405 | 8.4e-94 | G | Glycosyltransferase Family 4 | |||
NHEFJLLP_01406 | 1.1e-126 | M | Glycosyltransferase WbsX | |||
NHEFJLLP_01407 | 2.1e-17 | |||||
NHEFJLLP_01409 | 0.0 | uvrA2 | L | ABC transporter | ||
NHEFJLLP_01410 | 2.5e-46 | |||||
NHEFJLLP_01411 | 1e-90 | |||||
NHEFJLLP_01412 | 1.6e-85 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_01413 | 2e-27 | S | Protein of unknown function (DUF1093) | |||
NHEFJLLP_01416 | 1.4e-84 | L | Integrase | |||
NHEFJLLP_01417 | 4.8e-44 | T | Antidote-toxin recognition MazE, bacterial antitoxin | |||
NHEFJLLP_01418 | 4.9e-57 | pemK | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
NHEFJLLP_01419 | 6.8e-28 | |||||
NHEFJLLP_01420 | 1.4e-226 | mdtG | EGP | Major facilitator Superfamily | ||
NHEFJLLP_01421 | 3e-51 | cadC1 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
NHEFJLLP_01422 | 8.1e-216 | yeaN | P | Transporter, major facilitator family protein | ||
NHEFJLLP_01424 | 3.4e-160 | S | reductase | |||
NHEFJLLP_01425 | 1.2e-165 | 1.1.1.65 | C | Aldo keto reductase | ||
NHEFJLLP_01426 | 2e-37 | cps4I | M | Glycosyltransferase like family 2 | ||
NHEFJLLP_01427 | 1.3e-87 | cps4I | M | Glycosyltransferase like family 2 | ||
NHEFJLLP_01428 | 3.1e-262 | cps4J | S | Polysaccharide biosynthesis protein | ||
NHEFJLLP_01429 | 4.5e-252 | cpdA | S | Calcineurin-like phosphoesterase | ||
NHEFJLLP_01430 | 2.3e-120 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
NHEFJLLP_01432 | 0.0 | uvrA2 | L | ABC transporter | ||
NHEFJLLP_01433 | 4.7e-246 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
NHEFJLLP_01434 | 3.4e-310 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
NHEFJLLP_01435 | 4e-46 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
NHEFJLLP_01436 | 3.8e-78 | ywiB | S | Domain of unknown function (DUF1934) | ||
NHEFJLLP_01437 | 3.3e-158 | dprA | LU | DNA protecting protein DprA | ||
NHEFJLLP_01438 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
NHEFJLLP_01439 | 6.6e-251 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
NHEFJLLP_01440 | 5.8e-177 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
NHEFJLLP_01441 | 6.7e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
NHEFJLLP_01442 | 1.1e-256 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
NHEFJLLP_01443 | 2.2e-170 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
NHEFJLLP_01444 | 6.7e-105 | 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 | |
NHEFJLLP_01445 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NHEFJLLP_01446 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
NHEFJLLP_01447 | 1.2e-177 | K | Transcriptional regulator | |||
NHEFJLLP_01448 | 1.7e-168 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
NHEFJLLP_01449 | 4e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
NHEFJLLP_01450 | 1e-95 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
NHEFJLLP_01451 | 4.2e-32 | S | YozE SAM-like fold | |||
NHEFJLLP_01452 | 7.9e-157 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
NHEFJLLP_01453 | 5.5e-68 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
NHEFJLLP_01454 | 1.1e-167 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
NHEFJLLP_01455 | 6.2e-94 | K | transcriptional regulator | |||
NHEFJLLP_01456 | 4.4e-300 | norB | EGP | Major Facilitator | ||
NHEFJLLP_01457 | 1.4e-147 | cps1D | M | Domain of unknown function (DUF4422) | ||
NHEFJLLP_01458 | 1.1e-198 | cps3I | G | Acyltransferase family | ||
NHEFJLLP_01459 | 1.2e-202 | cps3H | ||||
NHEFJLLP_01460 | 1.4e-163 | cps3F | ||||
NHEFJLLP_01461 | 1.7e-145 | cps1D | M | Domain of unknown function (DUF4422) | ||
NHEFJLLP_01462 | 3.3e-200 | cps3I | G | Acyltransferase family | ||
NHEFJLLP_01463 | 6.5e-193 | cps3H | ||||
NHEFJLLP_01464 | 4.7e-165 | cps3F | ||||
NHEFJLLP_01465 | 1.9e-161 | vdlC | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | ||
NHEFJLLP_01466 | 4.5e-174 | rihC | 3.2.2.1 | F | Nucleoside | |
NHEFJLLP_01467 | 1.9e-69 | accB | 2.3.1.12 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
NHEFJLLP_01468 | 9.3e-80 | |||||
NHEFJLLP_01469 | 9.3e-83 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
NHEFJLLP_01470 | 6.3e-230 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_01471 | 1.7e-159 | L | hmm pf00665 | |||
NHEFJLLP_01472 | 4.4e-129 | L | Helix-turn-helix domain | |||
NHEFJLLP_01473 | 1.1e-56 | hxlR | K | HxlR-like helix-turn-helix | ||
NHEFJLLP_01474 | 4.9e-109 | XK27_07075 | V | CAAX protease self-immunity | ||
NHEFJLLP_01475 | 2.6e-198 | camS | S | sex pheromone | ||
NHEFJLLP_01476 | 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 | |
NHEFJLLP_01477 | 5.2e-226 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
NHEFJLLP_01478 | 1.4e-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 | |
NHEFJLLP_01479 | 9.6e-58 | |||||
NHEFJLLP_01480 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
NHEFJLLP_01481 | 8.5e-78 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
NHEFJLLP_01482 | 2.2e-116 | 3.1.3.18 | J | HAD-hyrolase-like | ||
NHEFJLLP_01483 | 1.9e-195 | tarK | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
NHEFJLLP_01484 | 4.1e-192 | tarJ | 1.1.1.137, 1.1.1.303, 1.1.1.4, 1.1.1.405 | E | Catalyzes the NADPH dependent reduction of D-ribulose 5- phosphate to D-ribitol 5-phosphate | |
NHEFJLLP_01485 | 3.7e-128 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
NHEFJLLP_01486 | 1.6e-73 | azoR | I | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
NHEFJLLP_01487 | 2.3e-81 | rmaD | K | Transcriptional regulator | ||
NHEFJLLP_01489 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
NHEFJLLP_01490 | 6.1e-171 | K | Transcriptional regulator | |||
NHEFJLLP_01491 | 1.1e-46 | K | Helix-turn-helix domain | |||
NHEFJLLP_01492 | 1.2e-177 | 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) | |
NHEFJLLP_01493 | 1.2e-149 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
NHEFJLLP_01494 | 1.2e-207 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
NHEFJLLP_01495 | 6.6e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
NHEFJLLP_01496 | 2.7e-106 | gst | 2.5.1.18 | O | glutathione transferase activity | |
NHEFJLLP_01497 | 3e-32 | K | HxlR-like helix-turn-helix | |||
NHEFJLLP_01498 | 3e-61 | 1.1.1.219, 4.2.1.46 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
NHEFJLLP_01499 | 4.1e-86 | S | Alpha/beta hydrolase family | |||
NHEFJLLP_01500 | 1.6e-49 | K | LytTr DNA-binding domain | |||
NHEFJLLP_01501 | 9.9e-42 | S | Protein of unknown function (DUF3021) | |||
NHEFJLLP_01504 | 4.6e-90 | L | Resolvase, N terminal domain | |||
NHEFJLLP_01505 | 0.0 | 3.1.21.5, 3.6.4.12 | L | DEAD-like helicases superfamily | ||
NHEFJLLP_01508 | 9.7e-37 | L | SinI restriction endonuclease | |||
NHEFJLLP_01509 | 2.3e-137 | sinIM | 2.1.1.37 | L | Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family | |
NHEFJLLP_01511 | 3.9e-20 | S | by MetaGeneAnnotator | |||
NHEFJLLP_01512 | 1.6e-26 | 3.4.22.70 | M | Sortase family | ||
NHEFJLLP_01516 | 5.7e-97 | K | Primase C terminal 1 (PriCT-1) | |||
NHEFJLLP_01517 | 2.6e-134 | D | Cellulose biosynthesis protein BcsQ | |||
NHEFJLLP_01519 | 1.7e-19 | |||||
NHEFJLLP_01520 | 1.5e-146 | tatD | L | hydrolase, TatD family | ||
NHEFJLLP_01521 | 2.6e-95 | 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 | |
NHEFJLLP_01522 | 8e-160 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
NHEFJLLP_01523 | 3.2e-37 | veg | S | Biofilm formation stimulator VEG | ||
NHEFJLLP_01524 | 1.5e-163 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
NHEFJLLP_01525 | 3.4e-197 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
NHEFJLLP_01526 | 1.2e-108 | tdk | 2.7.1.21 | F | thymidine kinase | |
NHEFJLLP_01527 | 5.8e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
NHEFJLLP_01528 | 5.8e-38 | cobQ | S | glutamine amidotransferase | ||
NHEFJLLP_01529 | 3.8e-16 | |||||
NHEFJLLP_01530 | 1.3e-11 | S | Transglycosylase associated protein | |||
NHEFJLLP_01531 | 1.1e-71 | S | cog cog1302 | |||
NHEFJLLP_01532 | 1.9e-23 | S | Small integral membrane protein (DUF2273) | |||
NHEFJLLP_01533 | 2.4e-93 | |||||
NHEFJLLP_01534 | 1.8e-68 | L | Putative transposase of IS4/5 family (DUF4096) | |||
NHEFJLLP_01535 | 4.1e-82 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
NHEFJLLP_01536 | 1.3e-257 | 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 | ||
NHEFJLLP_01537 | 3.7e-205 | yacL | S | domain protein | ||
NHEFJLLP_01538 | 8.9e-289 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
NHEFJLLP_01539 | 6.2e-266 | yjeM | E | Amino Acid | ||
NHEFJLLP_01540 | 3.9e-66 | lysM | M | LysM domain | ||
NHEFJLLP_01541 | 1.3e-223 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
NHEFJLLP_01542 | 5.9e-73 | cvfB | S | S1 domain | ||
NHEFJLLP_01543 | 1.1e-164 | xerD | D | recombinase XerD | ||
NHEFJLLP_01544 | 4.8e-69 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NHEFJLLP_01545 | 8.2e-129 | 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 | ||
NHEFJLLP_01546 | 7.9e-103 | 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 | ||
NHEFJLLP_01547 | 9e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NHEFJLLP_01548 | 2.4e-193 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NHEFJLLP_01549 | 2.5e-289 | clcA | P | chloride | ||
NHEFJLLP_01550 | 1e-53 | licT | K | CAT RNA binding domain | ||
NHEFJLLP_01551 | 0.0 | bglP | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
NHEFJLLP_01552 | 3.2e-291 | pbg10 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_01553 | 0.0 | L | AAA domain | |||
NHEFJLLP_01554 | 8.2e-72 | L | AAA domain | |||
NHEFJLLP_01555 | 1.1e-116 | XK27_07075 | V | CAAX protease self-immunity | ||
NHEFJLLP_01556 | 1.9e-65 | S | Phage capsid family | |||
NHEFJLLP_01557 | 5.6e-24 | S | Phage gp6-like head-tail connector protein | |||
NHEFJLLP_01558 | 2e-13 | S | Phage head-tail joining protein | |||
NHEFJLLP_01559 | 5.2e-19 | |||||
NHEFJLLP_01560 | 5.6e-22 | |||||
NHEFJLLP_01561 | 4.3e-19 | S | Phage tail tube protein | |||
NHEFJLLP_01562 | 8.2e-125 | |||||
NHEFJLLP_01565 | 4.2e-171 | M | Phage tail tape measure protein TP901 | |||
NHEFJLLP_01566 | 3.2e-45 | S | Phage tail protein | |||
NHEFJLLP_01567 | 8.9e-60 | S | Phage minor structural protein | |||
NHEFJLLP_01568 | 2.6e-20 | S | Phage minor structural protein | |||
NHEFJLLP_01569 | 1.9e-79 | |||||
NHEFJLLP_01571 | 5.6e-86 | M | hydrolase, family 25 | |||
NHEFJLLP_01572 | 3.8e-11 | S | Haemolysin XhlA | |||
NHEFJLLP_01574 | 1.1e-115 | GM | NmrA-like family | |||
NHEFJLLP_01575 | 1.3e-81 | elaA | S | GNAT family | ||
NHEFJLLP_01576 | 1.6e-158 | EG | EamA-like transporter family | |||
NHEFJLLP_01577 | 1.8e-119 | S | membrane | |||
NHEFJLLP_01578 | 8.2e-109 | S | VIT family | |||
NHEFJLLP_01579 | 3.9e-111 | |||||
NHEFJLLP_01580 | 2.9e-150 | M | Glycosyl hydrolases family 25 | |||
NHEFJLLP_01581 | 2e-143 | yvpB | S | Peptidase_C39 like family | ||
NHEFJLLP_01582 | 1.1e-92 | yueI | S | Protein of unknown function (DUF1694) | ||
NHEFJLLP_01583 | 5.8e-216 | tarK | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
NHEFJLLP_01584 | 1.1e-192 | tarJ | 1.1.1.137, 1.1.1.303, 1.1.1.4, 1.1.1.405 | E | Catalyzes the NADPH dependent reduction of D-ribulose 5- phosphate to D-ribitol 5-phosphate | |
NHEFJLLP_01585 | 1.6e-126 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the transfer of the cytidylyl group of CTP to D-ribitol 5-phosphate | |
NHEFJLLP_01586 | 2e-180 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
NHEFJLLP_01587 | 3.3e-18 | oatA | I | Acyltransferase | ||
NHEFJLLP_01588 | 1.8e-22 | oatA | I | Acyltransferase | ||
NHEFJLLP_01589 | 1.5e-112 | M | ErfK YbiS YcfS YnhG | |||
NHEFJLLP_01590 | 4e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
NHEFJLLP_01591 | 1.9e-283 | ydfD | K | Alanine-glyoxylate amino-transferase | ||
NHEFJLLP_01592 | 1.4e-102 | argO | S | LysE type translocator | ||
NHEFJLLP_01593 | 0.0 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
NHEFJLLP_01594 | 1.3e-78 | S | Pyridoxamine 5'-phosphate oxidase | |||
NHEFJLLP_01595 | 1.6e-31 | cspA | K | Cold shock protein domain | ||
NHEFJLLP_01596 | 1.7e-37 | |||||
NHEFJLLP_01597 | 3.8e-53 | |||||
NHEFJLLP_01598 | 7.3e-33 | S | Protein of unknown function (DUF2922) | |||
NHEFJLLP_01599 | 7e-30 | |||||
NHEFJLLP_01600 | 6.2e-25 | |||||
NHEFJLLP_01601 | 4.4e-100 | K | DNA-templated transcription, initiation | |||
NHEFJLLP_01602 | 3.9e-125 | |||||
NHEFJLLP_01603 | 5e-114 | rhaS6 | K | helix_turn_helix, arabinose operon control protein | ||
NHEFJLLP_01604 | 4.2e-145 | I | Carboxylesterase family | |||
NHEFJLLP_01605 | 1.2e-155 | yhjX | P | Major Facilitator Superfamily | ||
NHEFJLLP_01606 | 7.3e-113 | bglK_1 | GK | ROK family | ||
NHEFJLLP_01607 | 2.4e-58 | 2.6.1.2, 2.6.1.66 | K | Bacteriophage CI repressor helix-turn-helix domain | ||
NHEFJLLP_01608 | 1.5e-255 | pepC | 3.4.22.40 | E | aminopeptidase | |
NHEFJLLP_01610 | 1.2e-108 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NHEFJLLP_01611 | 1.1e-302 | |||||
NHEFJLLP_01612 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
NHEFJLLP_01614 | 3.3e-37 | S | Haemolysin XhlA | |||
NHEFJLLP_01615 | 1.9e-173 | lys | M | Glycosyl hydrolases family 25 | ||
NHEFJLLP_01616 | 1.8e-54 | |||||
NHEFJLLP_01619 | 4e-236 | |||||
NHEFJLLP_01620 | 1.1e-283 | S | Phage minor structural protein | |||
NHEFJLLP_01621 | 9.8e-218 | S | Phage tail protein | |||
NHEFJLLP_01622 | 3.6e-54 | M | Membrane | |||
NHEFJLLP_01623 | 3.3e-192 | M | Phage tail tape measure protein TP901 | |||
NHEFJLLP_01624 | 2.2e-07 | |||||
NHEFJLLP_01625 | 1.3e-13 | S | Phage tail assembly chaperone proteins, TAC | |||
NHEFJLLP_01626 | 2.1e-75 | S | Phage tail tube protein | |||
NHEFJLLP_01627 | 2.5e-30 | S | Protein of unknown function (DUF806) | |||
NHEFJLLP_01628 | 5.4e-28 | S | Bacteriophage HK97-gp10, putative tail-component | |||
NHEFJLLP_01629 | 4.5e-18 | S | Phage head-tail joining protein | |||
NHEFJLLP_01630 | 2.2e-23 | S | Phage gp6-like head-tail connector protein | |||
NHEFJLLP_01631 | 1.6e-66 | S | Phage capsid family | |||
NHEFJLLP_01632 | 6.2e-146 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NHEFJLLP_01633 | 2.1e-171 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NHEFJLLP_01634 | 5.4e-124 | yliE | T | Putative diguanylate phosphodiesterase | ||
NHEFJLLP_01635 | 5.4e-170 | |||||
NHEFJLLP_01636 | 1.3e-219 | yibE | S | overlaps another CDS with the same product name | ||
NHEFJLLP_01637 | 1.3e-126 | yibF | S | overlaps another CDS with the same product name | ||
NHEFJLLP_01638 | 2.6e-103 | 3.2.2.20 | K | FR47-like protein | ||
NHEFJLLP_01639 | 5e-122 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
NHEFJLLP_01640 | 4.2e-118 | tagE1 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHEFJLLP_01641 | 1.6e-121 | |||||
NHEFJLLP_01642 | 4.1e-212 | 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 | |
NHEFJLLP_01643 | 8.2e-165 | 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 | |
NHEFJLLP_01644 | 2.1e-143 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
NHEFJLLP_01645 | 3.9e-150 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
NHEFJLLP_01646 | 1.3e-78 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
NHEFJLLP_01647 | 1.9e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
NHEFJLLP_01648 | 2e-100 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
NHEFJLLP_01649 | 1.1e-161 | rapZ | S | Displays ATPase and GTPase activities | ||
NHEFJLLP_01650 | 9.3e-87 | S | Short repeat of unknown function (DUF308) | |||
NHEFJLLP_01651 | 7.2e-264 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
NHEFJLLP_01652 | 3.3e-98 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
NHEFJLLP_01653 | 0.0 | ubiB | S | ABC1 family | ||
NHEFJLLP_01654 | 1.8e-108 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_01655 | 0.0 | mdlB | V | ABC transporter | ||
NHEFJLLP_01656 | 0.0 | mdlA | V | ABC transporter | ||
NHEFJLLP_01657 | 4.7e-45 | macB | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_01658 | 0.0 | ylbB | V | ABC transporter permease | ||
NHEFJLLP_01659 | 1.7e-235 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
NHEFJLLP_01660 | 2.7e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
NHEFJLLP_01661 | 1.6e-48 | yrzB | S | Belongs to the UPF0473 family | ||
NHEFJLLP_01662 | 7.3e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
NHEFJLLP_01663 | 2.4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
NHEFJLLP_01664 | 1.9e-297 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
NHEFJLLP_01665 | 1.2e-192 | pts30BCA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
NHEFJLLP_01666 | 1e-292 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_01667 | 1.1e-211 | S | Bacterial protein of unknown function (DUF871) | |||
NHEFJLLP_01668 | 1.9e-59 | 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 | ||
NHEFJLLP_01669 | 3.4e-140 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
NHEFJLLP_01670 | 8.2e-96 | 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 | ||
NHEFJLLP_01671 | 2.6e-39 | ylqC | S | Belongs to the UPF0109 family | ||
NHEFJLLP_01672 | 2.9e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
NHEFJLLP_01673 | 2.9e-220 | 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 | |
NHEFJLLP_01674 | 2.6e-58 | 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 | ||
NHEFJLLP_01675 | 5.6e-169 | 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) | ||
NHEFJLLP_01676 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
NHEFJLLP_01677 | 5.7e-129 | 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 | |
NHEFJLLP_01678 | 1.7e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NHEFJLLP_01679 | 6.7e-190 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
NHEFJLLP_01680 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
NHEFJLLP_01681 | 0.0 | yloV | S | DAK2 domain fusion protein YloV | ||
NHEFJLLP_01682 | 1.8e-57 | asp | S | Asp23 family, cell envelope-related function | ||
NHEFJLLP_01683 | 4.9e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
NHEFJLLP_01684 | 6.3e-96 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
NHEFJLLP_01685 | 6.8e-37 | lmrA | 3.6.3.44 | V | ABC transporter | |
NHEFJLLP_01686 | 5.6e-89 | |||||
NHEFJLLP_01687 | 0.0 | ybfG | M | peptidoglycan-binding domain-containing protein | ||
NHEFJLLP_01688 | 2e-129 | K | UTRA domain | |||
NHEFJLLP_01689 | 3.5e-85 | agaB | 2.7.1.191 | K | PTS system sorbose subfamily IIB component | |
NHEFJLLP_01690 | 4.7e-143 | agaC | G | PTS system sorbose-specific iic component | ||
NHEFJLLP_01691 | 3.2e-147 | G | PTS system mannose/fructose/sorbose family IID component | |||
NHEFJLLP_01692 | 3e-72 | G | PTS system fructose IIA component | |||
NHEFJLLP_01693 | 5.8e-40 | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | |||
NHEFJLLP_01694 | 2.4e-65 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
NHEFJLLP_01695 | 3.2e-43 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
NHEFJLLP_01696 | 0.0 | ctpA | 3.6.3.54 | P | P-type ATPase | |
NHEFJLLP_01697 | 1.6e-169 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NHEFJLLP_01698 | 1.3e-249 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_01700 | 7e-40 | |||||
NHEFJLLP_01701 | 9.3e-83 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
NHEFJLLP_01702 | 4.2e-09 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
NHEFJLLP_01703 | 8.6e-254 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
NHEFJLLP_01704 | 1.4e-150 | S | hydrolase | |||
NHEFJLLP_01705 | 6.5e-187 | murE | 6.3.2.10, 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
NHEFJLLP_01706 | 6.7e-254 | xylP2 | G | symporter | ||
NHEFJLLP_01707 | 9e-192 | nlhH_1 | I | alpha/beta hydrolase fold | ||
NHEFJLLP_01708 | 6e-65 | V | ABC transporter | |||
NHEFJLLP_01709 | 2.3e-51 | K | Helix-turn-helix domain | |||
NHEFJLLP_01710 | 2.7e-174 | P | Major Facilitator Superfamily | |||
NHEFJLLP_01711 | 9.2e-225 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
NHEFJLLP_01712 | 1.4e-98 | K | Helix-turn-helix domain | |||
NHEFJLLP_01713 | 1.1e-132 | |||||
NHEFJLLP_01714 | 1.3e-99 | K | DNA-templated transcription, initiation | |||
NHEFJLLP_01715 | 4.3e-26 | |||||
NHEFJLLP_01716 | 6.4e-31 | |||||
NHEFJLLP_01717 | 7.3e-33 | S | Protein of unknown function (DUF2922) | |||
NHEFJLLP_01718 | 3.8e-53 | |||||
NHEFJLLP_01719 | 1.1e-49 | M | Glycosyl transferases group 1 | |||
NHEFJLLP_01720 | 8e-26 | 2.3.1.79 | S | Bacterial transferase hexapeptide (six repeats) | ||
NHEFJLLP_01721 | 1.2e-194 | tra | L | Transposase and inactivated derivatives, IS30 family | ||
NHEFJLLP_01722 | 6e-93 | S | polysaccharide biosynthetic process | |||
NHEFJLLP_01724 | 3.3e-134 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
NHEFJLLP_01725 | 1.3e-107 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
NHEFJLLP_01726 | 5e-190 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
NHEFJLLP_01727 | 9.9e-152 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
NHEFJLLP_01728 | 2.3e-17 | V | VanZ like family | |||
NHEFJLLP_01729 | 8.7e-146 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NHEFJLLP_01731 | 3.2e-37 | S | Protein of unknown function (DUF2922) | |||
NHEFJLLP_01733 | 6.8e-99 | tnpR1 | L | Resolvase, N terminal domain | ||
NHEFJLLP_01734 | 7.2e-254 | fbp | 3.1.3.11 | G | phosphatase activity | |
NHEFJLLP_01735 | 1e-104 | kup | P | Transport of potassium into the cell | ||
NHEFJLLP_01736 | 1.1e-92 | acmA | 3.2.1.17 | NU | mannosyl-glycoprotein | |
NHEFJLLP_01737 | 9.1e-104 | 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 | |
NHEFJLLP_01738 | 4.7e-91 | S | UPF0316 protein | |||
NHEFJLLP_01739 | 1.3e-218 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
NHEFJLLP_01740 | 1e-190 | ampC | V | Beta-lactamase | ||
NHEFJLLP_01741 | 5.2e-29 | |||||
NHEFJLLP_01742 | 1e-203 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
NHEFJLLP_01743 | 0.0 | yjcE | P | Sodium proton antiporter | ||
NHEFJLLP_01744 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
NHEFJLLP_01745 | 6.7e-89 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
NHEFJLLP_01746 | 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 | ||
NHEFJLLP_01747 | 5.4e-228 | patA | 2.6.1.1 | E | Aminotransferase | |
NHEFJLLP_01748 | 1.1e-34 | ykuJ | S | Protein of unknown function (DUF1797) | ||
NHEFJLLP_01749 | 2.7e-79 | T | Universal stress protein family | |||
NHEFJLLP_01750 | 2.2e-99 | padR | K | Virulence activator alpha C-term | ||
NHEFJLLP_01751 | 1.7e-104 | padC | Q | Phenolic acid decarboxylase | ||
NHEFJLLP_01752 | 2.9e-156 | T | Calcineurin-like phosphoesterase superfamily domain | |||
NHEFJLLP_01753 | 2e-94 | K | Acetyltransferase (GNAT) domain | |||
NHEFJLLP_01754 | 3.4e-94 | |||||
NHEFJLLP_01755 | 6.4e-180 | P | secondary active sulfate transmembrane transporter activity | |||
NHEFJLLP_01756 | 3.4e-166 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
NHEFJLLP_01757 | 2.3e-69 | |||||
NHEFJLLP_01758 | 3.8e-131 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_01759 | 7.4e-176 | C | C4-dicarboxylate transmembrane transporter activity | |||
NHEFJLLP_01760 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
NHEFJLLP_01761 | 4.7e-73 | copR | K | Copper transport repressor CopY TcrY | ||
NHEFJLLP_01762 | 6.2e-51 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
NHEFJLLP_01763 | 4.6e-12 | |||||
NHEFJLLP_01764 | 2.5e-209 | pmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_01765 | 6.4e-125 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
NHEFJLLP_01766 | 1.3e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NHEFJLLP_01767 | 9.2e-270 | glnPH2 | P | ABC transporter permease | ||
NHEFJLLP_01768 | 4.3e-22 | |||||
NHEFJLLP_01769 | 9.9e-73 | S | Iron-sulphur cluster biosynthesis | |||
NHEFJLLP_01770 | 2.2e-49 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
NHEFJLLP_01771 | 5.1e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
NHEFJLLP_01772 | 3.3e-236 | 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 | ||
NHEFJLLP_01773 | 1.6e-212 | 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 | ||
NHEFJLLP_01774 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
NHEFJLLP_01775 | 1.1e-159 | S | Tetratricopeptide repeat | |||
NHEFJLLP_01776 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
NHEFJLLP_01777 | 6.2e-157 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NHEFJLLP_01778 | 3.7e-192 | mdtG | EGP | Major Facilitator Superfamily | ||
NHEFJLLP_01779 | 6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
NHEFJLLP_01780 | 1.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
NHEFJLLP_01781 | 1.1e-187 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
NHEFJLLP_01782 | 7.7e-120 | comEC | S | Competence protein ComEC | ||
NHEFJLLP_01783 | 1.9e-141 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
NHEFJLLP_01784 | 2.2e-99 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
NHEFJLLP_01785 | 3.5e-74 | yqhY | S | Asp23 family, cell envelope-related function | ||
NHEFJLLP_01786 | 5.2e-69 | 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 | ||
NHEFJLLP_01787 | 2.2e-151 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
NHEFJLLP_01788 | 2e-239 | yhjE | EGP | MFS transporter, metabolite H symporter (MHS) family protein | ||
NHEFJLLP_01789 | 7e-155 | tesE | Q | hydratase | ||
NHEFJLLP_01790 | 1.6e-174 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
NHEFJLLP_01791 | 1.3e-296 | yfgQ | P | E1-E2 ATPase | ||
NHEFJLLP_01792 | 8.2e-238 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_01793 | 1.3e-72 | |||||
NHEFJLLP_01794 | 0.0 | S | Bacterial membrane protein YfhO | |||
NHEFJLLP_01795 | 5.4e-71 | zmp2 | O | Zinc-dependent metalloprotease | ||
NHEFJLLP_01796 | 7.3e-258 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
NHEFJLLP_01797 | 3.2e-124 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
NHEFJLLP_01798 | 1.2e-51 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
NHEFJLLP_01799 | 3.6e-99 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
NHEFJLLP_01800 | 4.5e-85 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
NHEFJLLP_01801 | 0.0 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
NHEFJLLP_01802 | 2.6e-36 | cadA | P | P-type ATPase | ||
NHEFJLLP_01803 | 4.3e-121 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01804 | 8.5e-233 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
NHEFJLLP_01805 | 5.5e-118 | |||||
NHEFJLLP_01806 | 1.3e-64 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01807 | 1e-140 | XK27_06930 | S | ABC-2 family transporter protein | ||
NHEFJLLP_01808 | 6.2e-60 | S | Protein of unknown function (DUF1211) | |||
NHEFJLLP_01809 | 1.2e-52 | pva1 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
NHEFJLLP_01810 | 2.7e-120 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
NHEFJLLP_01812 | 3.7e-290 | QT | PucR C-terminal helix-turn-helix domain | |||
NHEFJLLP_01813 | 5e-113 | drgA | C | Nitroreductase family | ||
NHEFJLLP_01814 | 1.1e-33 | hol | S | Bacteriophage holin | ||
NHEFJLLP_01815 | 1.2e-34 | S | Haemolysin XhlA | |||
NHEFJLLP_01816 | 2.1e-200 | lys | M | Glycosyl hydrolases family 25 | ||
NHEFJLLP_01817 | 1.5e-22 | |||||
NHEFJLLP_01818 | 4.3e-61 | |||||
NHEFJLLP_01821 | 2.5e-227 | |||||
NHEFJLLP_01822 | 0.0 | S | Phage minor structural protein | |||
NHEFJLLP_01823 | 0.0 | S | Phage tail protein | |||
NHEFJLLP_01824 | 0.0 | S | peptidoglycan catabolic process | |||
NHEFJLLP_01827 | 3.2e-70 | S | Phage tail tube protein | |||
NHEFJLLP_01828 | 1e-26 | |||||
NHEFJLLP_01829 | 7.7e-39 | |||||
NHEFJLLP_01830 | 4e-25 | S | Phage head-tail joining protein | |||
NHEFJLLP_01831 | 1e-46 | S | Phage gp6-like head-tail connector protein | |||
NHEFJLLP_01832 | 1.4e-210 | S | peptidase activity | |||
NHEFJLLP_01833 | 2.7e-124 | S | Clp protease | |||
NHEFJLLP_01834 | 3.5e-219 | S | Phage portal protein | |||
NHEFJLLP_01835 | 2.1e-25 | S | Protein of unknown function (DUF1056) | |||
NHEFJLLP_01836 | 0.0 | S | Phage Terminase | |||
NHEFJLLP_01837 | 3.6e-79 | S | Phage terminase, small subunit | |||
NHEFJLLP_01840 | 1.7e-90 | L | HNH nucleases | |||
NHEFJLLP_01844 | 4.1e-10 | |||||
NHEFJLLP_01845 | 2.1e-65 | S | Transcriptional regulator, RinA family | |||
NHEFJLLP_01846 | 2.3e-15 | |||||
NHEFJLLP_01847 | 2.9e-38 | |||||
NHEFJLLP_01848 | 3.5e-19 | S | YopX protein | |||
NHEFJLLP_01850 | 2e-11 | |||||
NHEFJLLP_01851 | 2.3e-45 | |||||
NHEFJLLP_01853 | 9.2e-144 | pi346 | L | IstB-like ATP binding protein | ||
NHEFJLLP_01854 | 2.5e-32 | ybl78 | L | Conserved phage C-terminus (Phg_2220_C) | ||
NHEFJLLP_01857 | 7.3e-17 | |||||
NHEFJLLP_01864 | 3.1e-69 | S | DNA binding | |||
NHEFJLLP_01866 | 9.8e-18 | ps115 | K | Cro/C1-type HTH DNA-binding domain | ||
NHEFJLLP_01869 | 1.2e-41 | S | Membrane | |||
NHEFJLLP_01879 | 2e-78 | int | L | Belongs to the 'phage' integrase family | ||
NHEFJLLP_01880 | 1.7e-139 | cysA | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_01881 | 0.0 | V | FtsX-like permease family | |||
NHEFJLLP_01882 | 8e-42 | |||||
NHEFJLLP_01883 | 7.9e-61 | gntR1 | K | Transcriptional regulator, GntR family | ||
NHEFJLLP_01884 | 6.9e-164 | V | ABC transporter, ATP-binding protein | |||
NHEFJLLP_01885 | 5.8e-149 | |||||
NHEFJLLP_01886 | 6.7e-81 | uspA | T | universal stress protein | ||
NHEFJLLP_01887 | 1.2e-35 | |||||
NHEFJLLP_01888 | 4.2e-71 | gtcA | S | Teichoic acid glycosylation protein | ||
NHEFJLLP_01889 | 4.3e-88 | |||||
NHEFJLLP_01890 | 2.7e-49 | |||||
NHEFJLLP_01892 | 1.7e-234 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
NHEFJLLP_01893 | 7.3e-86 | 2.7.7.1, 3.6.1.55 | F | belongs to the nudix hydrolase family | ||
NHEFJLLP_01894 | 5.4e-118 | |||||
NHEFJLLP_01895 | 1.5e-52 | |||||
NHEFJLLP_01897 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
NHEFJLLP_01898 | 3.6e-282 | thrC | 4.2.3.1 | E | Threonine synthase | |
NHEFJLLP_01899 | 4.5e-146 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
NHEFJLLP_01900 | 1.5e-11 | mcbG | S | Pentapeptide repeats (8 copies) | ||
NHEFJLLP_01901 | 1.7e-41 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
NHEFJLLP_01902 | 1.1e-112 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NHEFJLLP_01903 | 1.4e-83 | |||||
NHEFJLLP_01904 | 1.9e-86 | yvbK | 3.1.3.25 | K | GNAT family | |
NHEFJLLP_01905 | 7e-37 | |||||
NHEFJLLP_01906 | 8.2e-48 | |||||
NHEFJLLP_01907 | 1.7e-111 | pgm8 | G | Histidine phosphatase superfamily (branch 1) | ||
NHEFJLLP_01909 | 2e-38 | |||||
NHEFJLLP_01910 | 1.4e-43 | |||||
NHEFJLLP_01911 | 7.3e-83 | K | MarR family | |||
NHEFJLLP_01912 | 0.0 | bztC | D | nuclear chromosome segregation | ||
NHEFJLLP_01913 | 3.7e-105 | yhdG | E | C-terminus of AA_permease | ||
NHEFJLLP_01915 | 0.0 | kup | P | Transport of potassium into the cell | ||
NHEFJLLP_01916 | 1.8e-99 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
NHEFJLLP_01917 | 7.4e-77 | argR | K | Regulates arginine biosynthesis genes | ||
NHEFJLLP_01918 | 4e-150 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
NHEFJLLP_01919 | 4.1e-159 | 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 | |
NHEFJLLP_01920 | 4.3e-33 | 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 | |
NHEFJLLP_01921 | 7.3e-101 | 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 | |
NHEFJLLP_01922 | 9e-39 | L | nuclease | |||
NHEFJLLP_01923 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
NHEFJLLP_01924 | 3.6e-64 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
NHEFJLLP_01925 | 1e-54 | |||||
NHEFJLLP_01926 | 3e-36 | K | Transcriptional regulator | |||
NHEFJLLP_01927 | 3.5e-66 | dltE | S | Enoyl-(Acyl carrier protein) reductase | ||
NHEFJLLP_01928 | 2.3e-08 | L | transposase activity | |||
NHEFJLLP_01929 | 2.1e-39 | ypaH | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
NHEFJLLP_01930 | 3.7e-172 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
NHEFJLLP_01931 | 1.8e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
NHEFJLLP_01932 | 1.1e-94 | G | Glycosyl hydrolases family 8 | |||
NHEFJLLP_01933 | 2.1e-180 | ydaM | M | Glycosyl transferase family group 2 | ||
NHEFJLLP_01934 | 7.2e-41 | |||||
NHEFJLLP_01935 | 6.2e-178 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
NHEFJLLP_01936 | 3.6e-39 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01937 | 1.4e-94 | degV | S | EDD domain protein, DegV family | ||
NHEFJLLP_01938 | 4.4e-94 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
NHEFJLLP_01939 | 7.7e-176 | 3.4.13.9 | E | Metallopeptidase family M24 | ||
NHEFJLLP_01940 | 5.2e-51 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_01941 | 2e-16 | |||||
NHEFJLLP_01943 | 1e-47 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
NHEFJLLP_01944 | 2.7e-251 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
NHEFJLLP_01945 | 2.8e-57 | T | Belongs to the universal stress protein A family | |||
NHEFJLLP_01946 | 7e-60 | tnpR1 | L | Resolvase, N terminal domain | ||
NHEFJLLP_01947 | 4.2e-11 | tnpR1 | L | Resolvase, N terminal domain | ||
NHEFJLLP_01948 | 5.7e-59 | K | Psort location Cytoplasmic, score | |||
NHEFJLLP_01949 | 9.1e-128 | hoxN | U | High-affinity nickel-transport protein | ||
NHEFJLLP_01950 | 1.8e-280 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NHEFJLLP_01951 | 8.6e-162 | 1.1.1.219 | GM | Male sterility protein | ||
NHEFJLLP_01952 | 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 | ||
NHEFJLLP_01953 | 5.5e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
NHEFJLLP_01954 | 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 | ||
NHEFJLLP_01955 | 1.5e-277 | pipD | E | Dipeptidase | ||
NHEFJLLP_01956 | 9.9e-199 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
NHEFJLLP_01957 | 1.9e-66 | K | Transcriptional regulator | |||
NHEFJLLP_01958 | 7e-161 | degV | S | EDD domain protein, DegV family | ||
NHEFJLLP_01959 | 5.4e-77 | yjcF | 3.5.4.33, 4.4.1.8 | K | protein acetylation | |
NHEFJLLP_01960 | 3.8e-131 | S | Protein of unknown function (DUF975) | |||
NHEFJLLP_01961 | 1.6e-146 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
NHEFJLLP_01962 | 4.8e-49 | S | Family of unknown function (DUF5388) | |||
NHEFJLLP_01964 | 2.5e-97 | L | PFAM Integrase catalytic region | |||
NHEFJLLP_01965 | 7.6e-255 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
NHEFJLLP_01966 | 5.4e-98 | yieF | S | NADPH-dependent FMN reductase | ||
NHEFJLLP_01967 | 9.3e-212 | tdcC | E | amino acid | ||
NHEFJLLP_01968 | 9.8e-123 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
NHEFJLLP_01969 | 7.6e-158 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
NHEFJLLP_01970 | 1.5e-126 | tuaA | M | Bacterial sugar transferase | ||
NHEFJLLP_01971 | 9.6e-180 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
NHEFJLLP_01972 | 2e-146 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NHEFJLLP_01973 | 3e-128 | yhgF | K | Tex-like protein N-terminal domain protein | ||
NHEFJLLP_01974 | 2.2e-81 | ydcK | S | Belongs to the SprT family | ||
NHEFJLLP_01975 | 4e-237 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
NHEFJLLP_01976 | 1.6e-157 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
NHEFJLLP_01979 | 9.2e-166 | yjjH | S | Calcineurin-like phosphoesterase | ||
NHEFJLLP_01980 | 5e-252 | dtpT | U | amino acid peptide transporter | ||
NHEFJLLP_01982 | 4.4e-42 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
NHEFJLLP_01991 | 6.6e-35 | S | Protein of unknown function (DUF3102) | |||
NHEFJLLP_01995 | 1e-12 | |||||
NHEFJLLP_01996 | 4.3e-97 | M | CHAP domain | |||
NHEFJLLP_01998 | 2.8e-125 | U | type IV secretory pathway VirB4 | |||
NHEFJLLP_01999 | 9.5e-17 | |||||
NHEFJLLP_02001 | 2e-28 | I | mechanosensitive ion channel activity | |||
NHEFJLLP_02003 | 8.6e-81 | K | AsnC family | |||
NHEFJLLP_02004 | 2e-35 | |||||
NHEFJLLP_02005 | 5.1e-34 | |||||
NHEFJLLP_02006 | 8.6e-218 | 2.7.7.65 | T | diguanylate cyclase | ||
NHEFJLLP_02007 | 7.1e-43 | |||||
NHEFJLLP_02008 | 1e-201 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
NHEFJLLP_02009 | 3.5e-154 | tagG | U | Transport permease protein | ||
NHEFJLLP_02010 | 5.3e-125 | |||||
NHEFJLLP_02011 | 0.0 | yfiC | V | ABC transporter | ||
NHEFJLLP_02012 | 3.1e-75 | ycfI | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02013 | 1.9e-80 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
NHEFJLLP_02014 | 1.7e-148 | pbpX | V | Beta-lactamase | ||
NHEFJLLP_02015 | 1.8e-170 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
NHEFJLLP_02016 | 1.5e-135 | fruR | K | DeoR C terminal sensor domain | ||
NHEFJLLP_02017 | 1.1e-222 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NHEFJLLP_02018 | 9e-209 | cps3D | ||||
NHEFJLLP_02019 | 1.1e-62 | S | Domain of unknown function (DUF4828) | |||
NHEFJLLP_02020 | 2.7e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
NHEFJLLP_02021 | 8.4e-190 | mocA | S | Oxidoreductase | ||
NHEFJLLP_02022 | 2.5e-115 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
NHEFJLLP_02023 | 1.6e-113 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
NHEFJLLP_02024 | 2.1e-117 | K | Helix-turn-helix domain, rpiR family | |||
NHEFJLLP_02025 | 1.5e-80 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
NHEFJLLP_02026 | 2.3e-113 | ppaX_1 | 3.1.3.18, 3.6.1.1 | S | haloacid dehalogenase-like hydrolase | |
NHEFJLLP_02027 | 1.1e-231 | gatC | G | PTS system sugar-specific permease component | ||
NHEFJLLP_02028 | 1.1e-44 | 2.7.1.194, 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
NHEFJLLP_02029 | 8.1e-79 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NHEFJLLP_02030 | 4.7e-141 | aRA11 | 1.1.1.346 | S | reductase | |
NHEFJLLP_02031 | 3.3e-82 | yiiE | S | Protein of unknown function (DUF1211) | ||
NHEFJLLP_02032 | 4.2e-76 | darA | C | Flavodoxin | ||
NHEFJLLP_02033 | 3e-126 | IQ | reductase | |||
NHEFJLLP_02034 | 8.1e-85 | glcU | U | sugar transport | ||
NHEFJLLP_02035 | 2.5e-86 | GM | NAD(P)H-binding | |||
NHEFJLLP_02036 | 6.4e-109 | akr5f | 1.1.1.346 | S | reductase | |
NHEFJLLP_02037 | 2e-78 | K | Transcriptional regulator | |||
NHEFJLLP_02039 | 1.8e-25 | fldA | C | Flavodoxin | ||
NHEFJLLP_02040 | 2.8e-20 | adhR | K | helix_turn_helix, mercury resistance | ||
NHEFJLLP_02041 | 5e-115 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_02042 | 2.2e-130 | C | Aldo keto reductase | |||
NHEFJLLP_02043 | 5.2e-140 | akr5f | 1.1.1.346 | S | reductase | |
NHEFJLLP_02044 | 8.1e-140 | EGP | Major Facilitator Superfamily | |||
NHEFJLLP_02045 | 5.7e-83 | GM | NAD(P)H-binding | |||
NHEFJLLP_02046 | 1e-109 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_02047 | 1.7e-93 | Z012_04635 | K | Helix-turn-helix XRE-family like proteins | ||
NHEFJLLP_02048 | 2.4e-34 | |||||
NHEFJLLP_02049 | 6.1e-19 | S | Barstar (barnase inhibitor) | |||
NHEFJLLP_02050 | 8.1e-119 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
NHEFJLLP_02051 | 3.7e-103 | uhpT | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02052 | 1e-72 | uhpT | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02053 | 6e-174 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
NHEFJLLP_02054 | 9.8e-104 | opuCB | E | ABC transporter permease | ||
NHEFJLLP_02055 | 5.7e-222 | opuCA | 3.6.3.32 | E | ABC transporter, ATP-binding protein | |
NHEFJLLP_02056 | 5.3e-107 | ecsB | U | ABC transporter | ||
NHEFJLLP_02057 | 3.2e-152 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
NHEFJLLP_02058 | 1.7e-120 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
NHEFJLLP_02059 | 1.6e-54 | ytzB | S | Peptidase propeptide and YPEB domain | ||
NHEFJLLP_02060 | 8.1e-55 | S | SMI1-KNR4 cell-wall | |||
NHEFJLLP_02061 | 6.2e-37 | S | Uncharacterized protein conserved in bacteria (DUF2247) | |||
NHEFJLLP_02062 | 2.2e-133 | cps3A | S | Glycosyltransferase like family 2 | ||
NHEFJLLP_02063 | 7.9e-44 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_02064 | 6e-78 | S | X-Pro dipeptidyl-peptidase (S15 family) | |||
NHEFJLLP_02065 | 6.5e-59 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_02066 | 1.1e-08 | C | Flavodoxin | |||
NHEFJLLP_02067 | 1.5e-42 | S | COG NOG38524 non supervised orthologous group | |||
NHEFJLLP_02068 | 1.1e-101 | G | Glycogen debranching enzyme | |||
NHEFJLLP_02069 | 4.4e-60 | repA | S | Replication initiator protein A | ||
NHEFJLLP_02070 | 2.1e-76 | Q | Methyltransferase | |||
NHEFJLLP_02071 | 4.4e-40 | |||||
NHEFJLLP_02072 | 2.4e-22 | |||||
NHEFJLLP_02073 | 3.3e-129 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
NHEFJLLP_02074 | 2e-42 | |||||
NHEFJLLP_02075 | 9.9e-82 | hit | FG | histidine triad | ||
NHEFJLLP_02076 | 1.6e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02077 | 2.1e-100 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
NHEFJLLP_02078 | 5.8e-172 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
NHEFJLLP_02079 | 7.3e-189 | arlS | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_02080 | 2.3e-12 | rfbP | M | Bacterial sugar transferase | ||
NHEFJLLP_02081 | 4.9e-212 | L | Transposase DDE domain | |||
NHEFJLLP_02082 | 7.5e-68 | epsE | M | Bacterial sugar transferase | ||
NHEFJLLP_02083 | 3.2e-71 | tnp2PF3 | L | manually curated | ||
NHEFJLLP_02085 | 2.1e-130 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
NHEFJLLP_02086 | 2.4e-168 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
NHEFJLLP_02087 | 1.2e-97 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
NHEFJLLP_02088 | 2.2e-138 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
NHEFJLLP_02089 | 1.4e-72 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
NHEFJLLP_02090 | 6e-109 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
NHEFJLLP_02091 | 2e-36 | M | Glycosyltransferase like family 2 | |||
NHEFJLLP_02092 | 5.9e-43 | J | Glycosyl transferase family 2 | |||
NHEFJLLP_02093 | 8.6e-27 | S | O-antigen ligase like membrane protein | |||
NHEFJLLP_02094 | 2.1e-104 | wcoF | M | Glycosyl transferases group 1 | ||
NHEFJLLP_02095 | 2.6e-164 | rgpAc | GT4 | M | glycosyl transferase group 1 | |
NHEFJLLP_02096 | 3.2e-86 | L | COG2801 Transposase and inactivated derivatives | |||
NHEFJLLP_02097 | 2.2e-72 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_02098 | 2.6e-239 | gshR1 | 1.8.1.7 | C | Glutathione reductase | |
NHEFJLLP_02099 | 2.1e-51 | |||||
NHEFJLLP_02100 | 1.9e-220 | S | CAAX protease self-immunity | |||
NHEFJLLP_02101 | 1.3e-271 | ybiT | S | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02102 | 1.1e-272 | ybiT | S | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02103 | 4.5e-222 | S | CAAX protease self-immunity | |||
NHEFJLLP_02104 | 6.9e-62 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NHEFJLLP_02105 | 5.2e-139 | |||||
NHEFJLLP_02106 | 5.8e-91 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
NHEFJLLP_02107 | 2.4e-130 | gntR2 | K | Transcriptional regulator | ||
NHEFJLLP_02108 | 7.8e-76 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_02109 | 5.5e-253 | gshR1 | 1.8.1.7 | C | Glutathione reductase | |
NHEFJLLP_02110 | 1.8e-66 | |||||
NHEFJLLP_02111 | 3.7e-107 | pncA | Q | Isochorismatase family | ||
NHEFJLLP_02112 | 2.7e-132 | |||||
NHEFJLLP_02113 | 5.1e-125 | skfE | V | ABC transporter | ||
NHEFJLLP_02114 | 9.5e-65 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
NHEFJLLP_02115 | 1.2e-45 | S | Enterocin A Immunity | |||
NHEFJLLP_02116 | 4.7e-45 | 2.1.1.14 | E | Methionine synthase | ||
NHEFJLLP_02117 | 3.9e-251 | pgaC | GT2 | M | Glycosyl transferase | |
NHEFJLLP_02118 | 4.4e-94 | |||||
NHEFJLLP_02119 | 4e-101 | T | EAL domain | |||
NHEFJLLP_02120 | 8.5e-102 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
NHEFJLLP_02121 | 2.6e-263 | ywfO | S | HD domain protein | ||
NHEFJLLP_02122 | 1.7e-148 | yxeH | S | hydrolase | ||
NHEFJLLP_02123 | 5.7e-117 | L | PFAM transposase, IS4 family protein | |||
NHEFJLLP_02124 | 1.8e-125 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
NHEFJLLP_02125 | 3.4e-136 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NHEFJLLP_02126 | 8.7e-215 | |||||
NHEFJLLP_02127 | 2.9e-187 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NHEFJLLP_02128 | 4.2e-30 | L | AAA domain | |||
NHEFJLLP_02129 | 3.5e-100 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
NHEFJLLP_02130 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
NHEFJLLP_02131 | 3.2e-203 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
NHEFJLLP_02132 | 1.2e-216 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
NHEFJLLP_02133 | 1.5e-132 | K | response regulator | |||
NHEFJLLP_02134 | 9.2e-251 | phoR | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_02135 | 3e-151 | pstS | P | Phosphate | ||
NHEFJLLP_02136 | 1.5e-161 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
NHEFJLLP_02137 | 1.5e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
NHEFJLLP_02138 | 1.1e-147 | 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 | |
NHEFJLLP_02139 | 1e-139 | 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 | |
NHEFJLLP_02140 | 5.4e-116 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
NHEFJLLP_02141 | 2e-49 | pspC | KT | positive regulation of macromolecule biosynthetic process | ||
NHEFJLLP_02142 | 9.2e-54 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
NHEFJLLP_02143 | 1.4e-176 | 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 | ||
NHEFJLLP_02144 | 3e-91 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_02145 | 7.3e-189 | S | Cell surface protein | |||
NHEFJLLP_02146 | 8.6e-63 | |||||
NHEFJLLP_02147 | 5.9e-48 | |||||
NHEFJLLP_02148 | 3.9e-57 | |||||
NHEFJLLP_02150 | 1.5e-163 | |||||
NHEFJLLP_02151 | 1.3e-72 | K | Transcriptional regulator | |||
NHEFJLLP_02152 | 3.8e-99 | pepF2 | E | Oligopeptidase F | ||
NHEFJLLP_02153 | 8.4e-268 | trpE | 4.1.3.27 | EH | Anthranilate synthase component I, N terminal region | |
NHEFJLLP_02154 | 1.5e-104 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | Peptidase C26 | |
NHEFJLLP_02155 | 4.4e-35 | yyaN | K | MerR HTH family regulatory protein | ||
NHEFJLLP_02156 | 1.3e-120 | azlC | E | branched-chain amino acid | ||
NHEFJLLP_02157 | 7.2e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
NHEFJLLP_02158 | 6.8e-209 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
NHEFJLLP_02159 | 2e-219 | pbpX1 | V | Beta-lactamase | ||
NHEFJLLP_02160 | 2.2e-63 | 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 | |
NHEFJLLP_02161 | 2.8e-93 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK) | |
NHEFJLLP_02162 | 2.6e-103 | folE | 2.7.6.3, 3.5.4.16 | F | GTP cyclohydrolase 1 | |
NHEFJLLP_02163 | 3e-175 | pepR1 | 3.4.11.5 | I | Releases the N-terminal proline from various substrates | |
NHEFJLLP_02164 | 9.8e-250 | puuP_1 | E | Amino acid permease | ||
NHEFJLLP_02167 | 8.8e-127 | 3.6.4.12 | L | Belongs to the 'phage' integrase family | ||
NHEFJLLP_02168 | 3.1e-170 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
NHEFJLLP_02169 | 6.1e-123 | pepL | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
NHEFJLLP_02170 | 1.8e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
NHEFJLLP_02171 | 1.4e-121 | pnb | C | nitroreductase | ||
NHEFJLLP_02172 | 5.2e-65 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
NHEFJLLP_02173 | 1.8e-116 | S | Elongation factor G-binding protein, N-terminal | |||
NHEFJLLP_02174 | 6.1e-168 | K | LysR substrate binding domain | |||
NHEFJLLP_02175 | 1.6e-146 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_02176 | 0.0 | S | Bacterial membrane protein YfhO | |||
NHEFJLLP_02177 | 7.1e-226 | nupG | F | Nucleoside | ||
NHEFJLLP_02178 | 7.1e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
NHEFJLLP_02179 | 2.7e-149 | noc | K | Belongs to the ParB family | ||
NHEFJLLP_02180 | 1.8e-136 | soj | D | Sporulation initiation inhibitor | ||
NHEFJLLP_02181 | 4.8e-157 | spo0J | K | Belongs to the ParB family | ||
NHEFJLLP_02182 | 1.7e-30 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
NHEFJLLP_02183 | 2e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
NHEFJLLP_02184 | 5.2e-125 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
NHEFJLLP_02185 | 2.3e-212 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
NHEFJLLP_02186 | 4.9e-210 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_02187 | 2e-71 | K | MarR family | |||
NHEFJLLP_02188 | 3.7e-149 | XK27_00825 | S | Sulfite exporter TauE/SafE | ||
NHEFJLLP_02189 | 3.9e-50 | |||||
NHEFJLLP_02190 | 1.4e-136 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | U | Ion channel | |
NHEFJLLP_02191 | 6.1e-171 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
NHEFJLLP_02192 | 4.4e-61 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
NHEFJLLP_02193 | 1.3e-42 | 3.6.4.13 | M | domain protein | ||
NHEFJLLP_02195 | 2.1e-157 | hipB | K | Helix-turn-helix | ||
NHEFJLLP_02196 | 2.8e-210 | oppA | E | ABC transporter, substratebinding protein | ||
NHEFJLLP_02197 | 1.9e-178 | 1.6.5.5 | C | Zinc-binding dehydrogenase | ||
NHEFJLLP_02198 | 2.8e-151 | larE | S | NAD synthase | ||
NHEFJLLP_02199 | 1.5e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_02200 | 2.6e-12 | larC | 4.99.1.12 | S | Protein of unknown function DUF111 | |
NHEFJLLP_02201 | 4.4e-129 | E | lipolytic protein G-D-S-L family | |||
NHEFJLLP_02202 | 4e-159 | yicL | EG | EamA-like transporter family | ||
NHEFJLLP_02203 | 5.2e-259 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NHEFJLLP_02204 | 2.1e-100 | yobS | K | Bacterial regulatory proteins, tetR family | ||
NHEFJLLP_02205 | 5.6e-170 | wbbI | M | transferase activity, transferring glycosyl groups | ||
NHEFJLLP_02206 | 5.3e-193 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NHEFJLLP_02207 | 4.1e-08 | rfbP | M | Bacterial sugar transferase | ||
NHEFJLLP_02208 | 3.7e-45 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NHEFJLLP_02209 | 2.9e-69 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
NHEFJLLP_02210 | 7.7e-274 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
NHEFJLLP_02211 | 7.8e-69 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
NHEFJLLP_02212 | 2.2e-134 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHEFJLLP_02213 | 1.8e-36 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
NHEFJLLP_02214 | 4.7e-100 | L | Integrase | |||
NHEFJLLP_02215 | 6.4e-31 | |||||
NHEFJLLP_02217 | 4.8e-157 | 1.6.5.2 | GM | NmrA-like family | ||
NHEFJLLP_02218 | 0.0 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
NHEFJLLP_02219 | 1.1e-126 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
NHEFJLLP_02220 | 1.4e-08 | |||||
NHEFJLLP_02221 | 2e-100 | S | NADPH-dependent FMN reductase | |||
NHEFJLLP_02222 | 2.3e-237 | S | module of peptide synthetase | |||
NHEFJLLP_02223 | 6.9e-107 | |||||
NHEFJLLP_02224 | 9.8e-88 | perR | P | Belongs to the Fur family | ||
NHEFJLLP_02225 | 7.1e-59 | S | Enterocin A Immunity | |||
NHEFJLLP_02226 | 5.4e-36 | S | Phospholipase_D-nuclease N-terminal | |||
NHEFJLLP_02227 | 1.8e-169 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
NHEFJLLP_02228 | 1.5e-103 | J | Acetyltransferase (GNAT) domain | |||
NHEFJLLP_02229 | 4.3e-63 | lrgA | S | LrgA family | ||
NHEFJLLP_02230 | 7.3e-127 | lrgB | M | LrgB-like family | ||
NHEFJLLP_02231 | 2.5e-145 | DegV | S | EDD domain protein, DegV family | ||
NHEFJLLP_02232 | 4.1e-25 | |||||
NHEFJLLP_02233 | 1.3e-117 | yugP | S | Putative neutral zinc metallopeptidase | ||
NHEFJLLP_02234 | 1.5e-61 | hxlR | K | Transcriptional regulator, HxlR family | ||
NHEFJLLP_02235 | 1.5e-135 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
NHEFJLLP_02236 | 1.1e-209 | pgaC | GT2 | M | Glycosyl transferase | |
NHEFJLLP_02237 | 1.8e-126 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NHEFJLLP_02238 | 8.1e-123 | tcyB | E | ABC transporter | ||
NHEFJLLP_02239 | 3.6e-137 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NHEFJLLP_02240 | 4.5e-82 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase like | ||
NHEFJLLP_02241 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
NHEFJLLP_02242 | 1.2e-179 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NHEFJLLP_02243 | 8.7e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
NHEFJLLP_02244 | 4.2e-115 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NHEFJLLP_02245 | 1.4e-99 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
NHEFJLLP_02246 | 8e-117 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
NHEFJLLP_02248 | 2.9e-162 | ypbG | 2.7.1.2 | GK | ROK family | |
NHEFJLLP_02249 | 1.4e-47 | 3.6.4.12 | K | HxlR-like helix-turn-helix | ||
NHEFJLLP_02250 | 2.1e-111 | K | Transcriptional regulator C-terminal region | |||
NHEFJLLP_02251 | 3.8e-204 | mdh | 1.1.1.350 | C | Belongs to the LDH2 MDH2 oxidoreductase family | |
NHEFJLLP_02252 | 1.5e-184 | ywhK | S | Membrane | ||
NHEFJLLP_02253 | 4.2e-62 | |||||
NHEFJLLP_02255 | 6.2e-108 | |||||
NHEFJLLP_02256 | 1.3e-53 | S | Uncharacterized protein conserved in bacteria (DUF2316) | |||
NHEFJLLP_02257 | 1.3e-15 | 4.1.1.46 | S | Amidohydrolase | ||
NHEFJLLP_02258 | 1.6e-129 | 4.1.1.46 | S | Amidohydrolase | ||
NHEFJLLP_02259 | 9.4e-118 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
NHEFJLLP_02260 | 3.4e-143 | yclK | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_02261 | 9.4e-217 | ywbD | 2.1.1.191 | J | S-adenosylmethionine-dependent methyltransferase | |
NHEFJLLP_02262 | 9.7e-155 | glcU | U | sugar transport | ||
NHEFJLLP_02263 | 1e-259 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NHEFJLLP_02264 | 6.8e-24 | |||||
NHEFJLLP_02265 | 0.0 | macB3 | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02266 | 2.9e-274 | tagE | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHEFJLLP_02267 | 0.0 | msbA2 | 3.6.3.44 | P | ABC transporter transmembrane region | |
NHEFJLLP_02268 | 1.6e-16 | |||||
NHEFJLLP_02269 | 1.9e-18 | |||||
NHEFJLLP_02270 | 1.6e-16 | |||||
NHEFJLLP_02271 | 1.6e-16 | |||||
NHEFJLLP_02272 | 1.6e-16 | |||||
NHEFJLLP_02273 | 1.1e-18 | |||||
NHEFJLLP_02274 | 5.2e-15 | |||||
NHEFJLLP_02275 | 7.2e-17 | |||||
NHEFJLLP_02276 | 2.7e-16 | |||||
NHEFJLLP_02278 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
NHEFJLLP_02279 | 7.9e-41 | |||||
NHEFJLLP_02280 | 1.9e-67 | tspO | T | TspO/MBR family | ||
NHEFJLLP_02281 | 6.3e-76 | uspA | T | Belongs to the universal stress protein A family | ||
NHEFJLLP_02282 | 8e-66 | S | Protein of unknown function (DUF805) | |||
NHEFJLLP_02283 | 1.3e-93 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
NHEFJLLP_02284 | 1.9e-47 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NHEFJLLP_02285 | 8.7e-235 | mepA | V | MATE efflux family protein | ||
NHEFJLLP_02287 | 3.4e-55 | K | Winged helix DNA-binding domain | |||
NHEFJLLP_02288 | 3.3e-166 | S | Oxidoreductase, aldo keto reductase family protein | |||
NHEFJLLP_02289 | 8.3e-162 | akr5f | 1.1.1.346 | S | reductase | |
NHEFJLLP_02290 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
NHEFJLLP_02291 | 3.5e-132 | S | ABC-2 family transporter protein | |||
NHEFJLLP_02292 | 1.4e-62 | S | Protein of unknown function | |||
NHEFJLLP_02293 | 2.5e-153 | EG | EamA-like transporter family | |||
NHEFJLLP_02294 | 2.5e-91 | MA20_25245 | K | FR47-like protein | ||
NHEFJLLP_02295 | 2e-126 | hchA | S | DJ-1/PfpI family | ||
NHEFJLLP_02296 | 1e-106 | |||||
NHEFJLLP_02297 | 4.4e-101 | S | Domain of unknown function (DUF4811) | |||
NHEFJLLP_02298 | 2.6e-226 | |||||
NHEFJLLP_02299 | 1.4e-48 | lldP | C | L-lactate permease | ||
NHEFJLLP_02300 | 2e-27 | lldP | C | L-lactate permease | ||
NHEFJLLP_02301 | 2.4e-66 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_02302 | 3.8e-120 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_02303 | 1e-155 | S | Phosphotransferase system, EIIC | |||
NHEFJLLP_02304 | 8.2e-134 | aroD | S | Alpha/beta hydrolase family | ||
NHEFJLLP_02305 | 3.2e-37 | |||||
NHEFJLLP_02307 | 4.1e-253 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
NHEFJLLP_02308 | 7.9e-21 | S | Virus attachment protein p12 family | |||
NHEFJLLP_02309 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
NHEFJLLP_02310 | 1.3e-34 | feoA | P | FeoA domain | ||
NHEFJLLP_02311 | 4.2e-144 | sufC | O | FeS assembly ATPase SufC | ||
NHEFJLLP_02312 | 1e-243 | sufD | O | FeS assembly protein SufD | ||
NHEFJLLP_02313 | 8e-235 | 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 | |
NHEFJLLP_02314 | 7.1e-83 | nifU | C | SUF system FeS assembly protein, NifU family | ||
NHEFJLLP_02315 | 1.4e-272 | sufB | O | assembly protein SufB | ||
NHEFJLLP_02316 | 5.5e-45 | yitW | S | Iron-sulfur cluster assembly protein | ||
NHEFJLLP_02317 | 3.1e-111 | hipB | K | Helix-turn-helix | ||
NHEFJLLP_02318 | 4.5e-121 | ybhL | S | Belongs to the BI1 family | ||
NHEFJLLP_02319 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
NHEFJLLP_02320 | 7.9e-100 | fadR | K | Bacterial regulatory proteins, tetR family | ||
NHEFJLLP_02321 | 3e-205 | 2.7.13.3 | T | GHKL domain | ||
NHEFJLLP_02322 | 1.8e-23 | |||||
NHEFJLLP_02323 | 3e-99 | S | ECF transporter, substrate-specific component | |||
NHEFJLLP_02324 | 5.8e-253 | yfnA | E | Amino Acid | ||
NHEFJLLP_02326 | 1.3e-62 | soj | D | AAA domain | ||
NHEFJLLP_02327 | 9.6e-189 | pacL | 3.6.3.8 | P | P-type ATPase | |
NHEFJLLP_02328 | 8.9e-72 | |||||
NHEFJLLP_02329 | 6.4e-157 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
NHEFJLLP_02330 | 8e-159 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
NHEFJLLP_02331 | 3e-30 | |||||
NHEFJLLP_02332 | 3e-122 | qmcA | O | prohibitin homologues | ||
NHEFJLLP_02333 | 2.4e-131 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
NHEFJLLP_02334 | 5.3e-125 | larB | S | AIR carboxylase | ||
NHEFJLLP_02335 | 2.6e-146 | larA | 5.1.2.1 | S | Domain of unknown function (DUF2088) | |
NHEFJLLP_02336 | 9.8e-106 | 3.2.2.20 | K | acetyltransferase | ||
NHEFJLLP_02337 | 7.8e-296 | S | ABC transporter, ATP-binding protein | |||
NHEFJLLP_02338 | 1.5e-241 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
NHEFJLLP_02339 | 1.1e-84 | hmpT | S | Pfam:DUF3816 | ||
NHEFJLLP_02340 | 1.1e-94 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_02341 | 1.6e-246 | V | Type II restriction enzyme, methylase subunits | |||
NHEFJLLP_02342 | 7.9e-13 | |||||
NHEFJLLP_02344 | 4.8e-17 | E | Pfam:DUF955 | |||
NHEFJLLP_02345 | 2e-24 | yvaO | K | Helix-turn-helix XRE-family like proteins | ||
NHEFJLLP_02346 | 2.5e-19 | |||||
NHEFJLLP_02347 | 1.2e-07 | |||||
NHEFJLLP_02348 | 8.9e-27 | S | Domain of unknown function (DUF771) | |||
NHEFJLLP_02354 | 1.5e-40 | S | Siphovirus Gp157 | |||
NHEFJLLP_02355 | 4e-157 | S | helicase activity | |||
NHEFJLLP_02356 | 6.6e-72 | L | AAA domain | |||
NHEFJLLP_02357 | 1.6e-26 | |||||
NHEFJLLP_02358 | 1.7e-76 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
NHEFJLLP_02359 | 8.2e-134 | S | Virulence-associated protein E | |||
NHEFJLLP_02360 | 2.2e-36 | S | hydrolase activity, acting on ester bonds | |||
NHEFJLLP_02364 | 3.7e-10 | |||||
NHEFJLLP_02366 | 1.6e-22 | |||||
NHEFJLLP_02371 | 2.5e-14 | S | Phage terminase, small subunit | |||
NHEFJLLP_02372 | 1.1e-181 | S | Phage Terminase | |||
NHEFJLLP_02373 | 6.1e-104 | S | Phage portal protein | |||
NHEFJLLP_02374 | 1.8e-56 | clpP | 3.4.21.92 | OU | Clp protease | |
NHEFJLLP_02375 | 1.5e-113 | S | Phage capsid family | |||
NHEFJLLP_02376 | 8.6e-14 | |||||
NHEFJLLP_02377 | 4.3e-25 | |||||
NHEFJLLP_02378 | 1.5e-33 | |||||
NHEFJLLP_02379 | 4.8e-22 | |||||
NHEFJLLP_02380 | 1.8e-38 | S | Phage tail tube protein | |||
NHEFJLLP_02383 | 2.6e-125 | M | Phage tail tape measure protein TP901 | |||
NHEFJLLP_02384 | 3.7e-25 | M | Phage tail tape measure protein TP901 | |||
NHEFJLLP_02385 | 6.9e-33 | S | Phage tail protein | |||
NHEFJLLP_02386 | 2.8e-217 | sidC | GT2,GT4 | LM | DNA recombination | |
NHEFJLLP_02387 | 8e-21 | S | Protein of unknown function (DUF1617) | |||
NHEFJLLP_02389 | 4.2e-41 | |||||
NHEFJLLP_02392 | 3.8e-109 | ps461 | M | Glycosyl hydrolases family 25 | ||
NHEFJLLP_02393 | 2.7e-55 | S | Putative inner membrane exporter, YdcZ | |||
NHEFJLLP_02394 | 2.1e-247 | iolT | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02395 | 1.3e-174 | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | ||
NHEFJLLP_02396 | 3.9e-190 | iolG | 1.1.1.18, 1.1.1.369 | C | Involved in the oxidation of myo-inositol (MI) and D- chiro-inositol (DCI) to 2-keto-myo-inositol (2KMI or 2-inosose) and 1-keto-D-chiro-inositol (1KDCI), respectively | |
NHEFJLLP_02397 | 2e-174 | iolE | 4.2.1.44 | G | Catalyzes the dehydration of inosose (2-keto-myo- inositol, 2KMI or 2,4,6 3,5-pentahydroxycyclohexanone) to 3D- (3,5 4)-trihydroxycyclohexane-1,2-dione (D-2,3-diketo-4-deoxy-epi- inositol) | |
NHEFJLLP_02398 | 1.2e-175 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
NHEFJLLP_02399 | 7.4e-241 | iolT | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02400 | 5e-182 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
NHEFJLLP_02401 | 1.3e-60 | S | Haem-degrading | |||
NHEFJLLP_02402 | 8.1e-147 | 3.5.1.10 | C | Alcohol dehydrogenase GroES-like domain | ||
NHEFJLLP_02403 | 2e-153 | rihA | F | Inosine-uridine preferring nucleoside hydrolase | ||
NHEFJLLP_02404 | 7.5e-73 | K | Helix-turn-helix domain, rpiR family | |||
NHEFJLLP_02405 | 3.7e-23 | K | Helix-turn-helix domain, rpiR family | |||
NHEFJLLP_02406 | 2.6e-12 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
NHEFJLLP_02407 | 4.6e-69 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
NHEFJLLP_02408 | 1.7e-83 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
NHEFJLLP_02409 | 1.2e-103 | GM | NAD(P)H-binding | |||
NHEFJLLP_02410 | 2.3e-195 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
NHEFJLLP_02411 | 1.4e-150 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHEFJLLP_02412 | 2.4e-181 | celE | 3.2.1.4 | GH5,GH9 | E | GDSL-like Lipase/Acylhydrolase family |
NHEFJLLP_02413 | 3.5e-177 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NHEFJLLP_02414 | 1.4e-173 | K | LytTr DNA-binding domain | |||
NHEFJLLP_02415 | 2.9e-148 | V | ABC transporter | |||
NHEFJLLP_02418 | 1.1e-31 | |||||
NHEFJLLP_02419 | 2.1e-244 | dinF | V | MatE | ||
NHEFJLLP_02420 | 3.3e-138 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NHEFJLLP_02421 | 3.5e-70 | 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) | ||
NHEFJLLP_02422 | 7e-192 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NHEFJLLP_02423 | 5.7e-95 | ccpB | 5.1.1.1 | K | lacI family | |
NHEFJLLP_02424 | 7.5e-101 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_02425 | 1.1e-62 | |||||
NHEFJLLP_02426 | 2.3e-150 | NU | Mycoplasma protein of unknown function, DUF285 | |||
NHEFJLLP_02427 | 2.1e-244 | cycA | E | Amino acid permease | ||
NHEFJLLP_02428 | 1.4e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NHEFJLLP_02429 | 1.8e-101 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
NHEFJLLP_02430 | 1.3e-114 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
NHEFJLLP_02431 | 1.4e-33 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
NHEFJLLP_02432 | 5.7e-180 | glk | 2.7.1.2 | G | Glucokinase | |
NHEFJLLP_02433 | 2.3e-17 | pepE | 3.4.13.21 | E | Belongs to the peptidase S51 family | |
NHEFJLLP_02434 | 3e-81 | pepE | 3.4.13.21 | E | Belongs to the peptidase S51 family | |
NHEFJLLP_02435 | 1.7e-67 | yqhL | P | Rhodanese-like protein | ||
NHEFJLLP_02436 | 6.9e-23 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
NHEFJLLP_02437 | 3.8e-139 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
NHEFJLLP_02438 | 9.2e-175 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
NHEFJLLP_02439 | 4.6e-64 | glnR | K | Transcriptional regulator | ||
NHEFJLLP_02440 | 6.2e-265 | glnA | 6.3.1.2 | E | glutamine synthetase | |
NHEFJLLP_02441 | 2e-161 | |||||
NHEFJLLP_02442 | 4e-181 | |||||
NHEFJLLP_02443 | 6.2e-99 | dut | S | Protein conserved in bacteria | ||
NHEFJLLP_02444 | 1.8e-56 | |||||
NHEFJLLP_02445 | 1.1e-29 | |||||
NHEFJLLP_02448 | 5.4e-19 | |||||
NHEFJLLP_02449 | 3.1e-89 | K | Transcriptional regulator | |||
NHEFJLLP_02450 | 7.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
NHEFJLLP_02451 | 3.2e-53 | ysxB | J | Cysteine protease Prp | ||
NHEFJLLP_02452 | 1.2e-117 | yfbR | S | HD containing hydrolase-like enzyme | ||
NHEFJLLP_02453 | 1.8e-27 | |||||
NHEFJLLP_02454 | 8.3e-201 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
NHEFJLLP_02455 | 4.1e-84 | uspA | T | Belongs to the universal stress protein A family | ||
NHEFJLLP_02456 | 6.3e-176 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
NHEFJLLP_02458 | 6.4e-54 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
NHEFJLLP_02459 | 3e-121 | yceE | S | haloacid dehalogenase-like hydrolase | ||
NHEFJLLP_02460 | 7.1e-159 | ccpB | 5.1.1.1 | K | lacI family | |
NHEFJLLP_02461 | 5.2e-164 | yvgN | C | Aldo keto reductase | ||
NHEFJLLP_02462 | 9.2e-133 | thrE | S | Putative threonine/serine exporter | ||
NHEFJLLP_02463 | 2e-77 | S | Threonine/Serine exporter, ThrE | |||
NHEFJLLP_02464 | 2.7e-75 | cpsE | M | Bacterial sugar transferase | ||
NHEFJLLP_02465 | 9.1e-54 | L | recombinase activity | |||
NHEFJLLP_02466 | 1.2e-67 | L | Integrase core domain | |||
NHEFJLLP_02467 | 4.7e-190 | asnB | 6.3.5.4 | E | Asparagine synthase | |
NHEFJLLP_02468 | 1.6e-219 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
NHEFJLLP_02469 | 1.1e-206 | |||||
NHEFJLLP_02470 | 1.8e-150 | S | Psort location Cytoplasmic, score | |||
NHEFJLLP_02471 | 3.6e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NHEFJLLP_02472 | 5.7e-258 | npr | 1.11.1.1 | C | NADH oxidase | |
NHEFJLLP_02473 | 6.4e-137 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02474 | 8.7e-154 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
NHEFJLLP_02475 | 1.4e-176 | XK27_08835 | S | ABC transporter | ||
NHEFJLLP_02476 | 1.1e-164 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
NHEFJLLP_02477 | 7.5e-244 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
NHEFJLLP_02478 | 7.3e-231 | hom1 | 1.1.1.3 | E | Homoserine dehydrogenase | |
NHEFJLLP_02479 | 5e-162 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
NHEFJLLP_02480 | 9.6e-191 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
NHEFJLLP_02481 | 0.0 | nagE | 2.7.1.193, 2.7.1.199, 2.7.1.211 | G | phosphotransferase system, EIIB | |
NHEFJLLP_02482 | 2.7e-39 | |||||
NHEFJLLP_02483 | 1.8e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
NHEFJLLP_02484 | 7.4e-18 | nagH | 2.7.13.3, 3.2.1.4, 3.2.1.52, 3.2.1.78, 3.2.1.8 | GH20,GH26,GH5,GH9 | M | MucBP domain |
NHEFJLLP_02485 | 7.5e-40 | sdrF | M | Collagen binding domain | ||
NHEFJLLP_02486 | 2.5e-269 | I | acetylesterase activity | |||
NHEFJLLP_02487 | 3.1e-84 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_02488 | 5.2e-192 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
NHEFJLLP_02489 | 2.4e-62 | M | domain protein | |||
NHEFJLLP_02490 | 1.1e-56 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_02491 | 3.7e-89 | tnpR1 | L | Resolvase, N terminal domain | ||
NHEFJLLP_02492 | 1.4e-78 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
NHEFJLLP_02493 | 1e-69 | |||||
NHEFJLLP_02494 | 7.7e-103 | L | Integrase | |||
NHEFJLLP_02495 | 3.4e-61 | |||||
NHEFJLLP_02496 | 9e-268 | tagE6 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHEFJLLP_02498 | 9.2e-53 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NHEFJLLP_02499 | 1.8e-54 | nudA | S | ASCH | ||
NHEFJLLP_02500 | 4.7e-108 | S | SdpI/YhfL protein family | |||
NHEFJLLP_02501 | 5.3e-92 | M | Lysin motif | |||
NHEFJLLP_02502 | 3.8e-254 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
NHEFJLLP_02503 | 1.8e-153 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
NHEFJLLP_02504 | 8.4e-131 | mntB | 3.6.3.35 | P | ABC transporter | |
NHEFJLLP_02505 | 4.8e-141 | mtsB | U | ABC 3 transport family | ||
NHEFJLLP_02506 | 7.9e-174 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NHEFJLLP_02507 | 3.1e-50 | |||||
NHEFJLLP_02508 | 4.6e-166 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NHEFJLLP_02509 | 1.7e-260 | citP | P | Sodium:sulfate symporter transmembrane region | ||
NHEFJLLP_02510 | 2.9e-179 | citR | K | sugar-binding domain protein | ||
NHEFJLLP_02511 | 5.1e-207 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
NHEFJLLP_02512 | 5.7e-189 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
NHEFJLLP_02513 | 9e-44 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
NHEFJLLP_02514 | 6.7e-162 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
NHEFJLLP_02515 | 1.3e-287 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
NHEFJLLP_02516 | 3.2e-62 | L | PFAM Integrase, catalytic core | |||
NHEFJLLP_02517 | 6.4e-40 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
NHEFJLLP_02518 | 1.1e-54 | ypaA | S | Protein of unknown function (DUF1304) | ||
NHEFJLLP_02519 | 3.6e-284 | mco | Q | Multicopper oxidase | ||
NHEFJLLP_02520 | 3.2e-141 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
NHEFJLLP_02521 | 3.3e-37 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_02522 | 1.1e-89 | V | VanZ like family | |||
NHEFJLLP_02523 | 1.5e-33 | |||||
NHEFJLLP_02524 | 1.9e-71 | spxA | 1.20.4.1 | P | ArsC family | |
NHEFJLLP_02526 | 1.9e-15 | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system, EIIB | ||
NHEFJLLP_02527 | 1e-139 | G | YdjC-like protein | |||
NHEFJLLP_02528 | 1.4e-212 | steT | E | amino acid | ||
NHEFJLLP_02529 | 2.1e-31 | |||||
NHEFJLLP_02530 | 1.7e-43 | ankB | S | ankyrin repeats | ||
NHEFJLLP_02531 | 1.9e-102 | M | Protein of unknown function (DUF3737) | |||
NHEFJLLP_02532 | 5.7e-194 | C | Aldo/keto reductase family | |||
NHEFJLLP_02533 | 2.9e-30 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
NHEFJLLP_02534 | 4.8e-137 | terC | P | membrane | ||
NHEFJLLP_02535 | 1.9e-158 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
NHEFJLLP_02536 | 1.1e-95 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
NHEFJLLP_02537 | 1e-145 | yxeH | S | hydrolase | ||
NHEFJLLP_02538 | 2.2e-115 | K | SIR2-like domain | |||
NHEFJLLP_02540 | 4.5e-70 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
NHEFJLLP_02541 | 9.6e-185 | ynfM | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02543 | 9.9e-230 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_02549 | 4.8e-75 | E | IrrE N-terminal-like domain | |||
NHEFJLLP_02550 | 1.7e-39 | yvaO | K | Helix-turn-helix domain | ||
NHEFJLLP_02555 | 7.3e-95 | |||||
NHEFJLLP_02557 | 4.3e-14 | S | Domain of unknown function (DUF1508) | |||
NHEFJLLP_02558 | 8.3e-85 | D | nuclear chromosome segregation | |||
NHEFJLLP_02559 | 2.7e-69 | |||||
NHEFJLLP_02560 | 2.4e-61 | S | Beta-lactamase superfamily domain | |||
NHEFJLLP_02561 | 1.5e-153 | L | DnaD domain protein | |||
NHEFJLLP_02562 | 6.3e-50 | |||||
NHEFJLLP_02563 | 3.5e-65 | ps308 | K | AntA/AntB antirepressor | ||
NHEFJLLP_02564 | 3.1e-63 | |||||
NHEFJLLP_02565 | 3.2e-65 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
NHEFJLLP_02567 | 7.9e-85 | S | methyltransferase activity | |||
NHEFJLLP_02569 | 1.5e-09 | S | YopX protein | |||
NHEFJLLP_02570 | 1.6e-23 | |||||
NHEFJLLP_02572 | 2.6e-250 | yifK | E | Amino acid permease | ||
NHEFJLLP_02573 | 9.9e-85 | F | NUDIX domain | |||
NHEFJLLP_02574 | 2.5e-155 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
NHEFJLLP_02575 | 1.5e-50 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NHEFJLLP_02576 | 6.6e-95 | S | Protein of unknown function (DUF1440) | |||
NHEFJLLP_02577 | 5.2e-174 | hrtB | V | ABC transporter permease | ||
NHEFJLLP_02578 | 9.3e-135 | ydjP | I | Alpha/beta hydrolase family | ||
NHEFJLLP_02579 | 6.2e-122 | E | GDSL-like Lipase/Acylhydrolase family | |||
NHEFJLLP_02580 | 1.4e-77 | |||||
NHEFJLLP_02581 | 9e-37 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
NHEFJLLP_02582 | 3.3e-97 | FG | HIT domain | |||
NHEFJLLP_02583 | 4.5e-61 | |||||
NHEFJLLP_02584 | 4.2e-92 | M1-874 | K | Domain of unknown function (DUF1836) | ||
NHEFJLLP_02585 | 1.6e-115 | S | Protein of unknown function (DUF554) | |||
NHEFJLLP_02586 | 1.9e-147 | KT | helix_turn_helix, mercury resistance | |||
NHEFJLLP_02587 | 8.7e-72 | asp | S | Asp23 family, cell envelope-related function | ||
NHEFJLLP_02588 | 7.2e-23 | |||||
NHEFJLLP_02589 | 2.6e-84 | |||||
NHEFJLLP_02590 | 7.1e-37 | S | Transglycosylase associated protein | |||
NHEFJLLP_02591 | 4.9e-172 | K | AI-2E family transporter | |||
NHEFJLLP_02592 | 7.9e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NHEFJLLP_02593 | 8.8e-40 | |||||
NHEFJLLP_02594 | 6.6e-92 | larE | S | NAD synthase | ||
NHEFJLLP_02595 | 1.6e-110 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_02596 | 3.3e-48 | L | Helix-turn-helix domain | |||
NHEFJLLP_02597 | 1.9e-43 | L | hmm pf00665 | |||
NHEFJLLP_02598 | 3e-79 | L | hmm pf00665 | |||
NHEFJLLP_02602 | 2.2e-98 | L | COG3547 Transposase and inactivated derivatives | |||
NHEFJLLP_02603 | 1.1e-34 | L | COG3547 Transposase and inactivated derivatives | |||
NHEFJLLP_02605 | 2e-117 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
NHEFJLLP_02606 | 5.5e-100 | K | Primase C terminal 1 (PriCT-1) | |||
NHEFJLLP_02608 | 6.8e-14 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_02610 | 1.2e-188 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
NHEFJLLP_02611 | 1.5e-107 | mmuP | E | amino acid | ||
NHEFJLLP_02612 | 1.8e-210 | natB | CP | ABC-2 family transporter protein | ||
NHEFJLLP_02613 | 1e-128 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
NHEFJLLP_02615 | 7.1e-35 | |||||
NHEFJLLP_02616 | 2.2e-42 | S | Protein of unknown function (DUF3037) | |||
NHEFJLLP_02617 | 1.2e-287 | S | Bacterial membrane protein, YfhO | |||
NHEFJLLP_02618 | 5.8e-143 | 2.4.2.3 | F | Phosphorylase superfamily | ||
NHEFJLLP_02619 | 1.6e-28 | KT | PspC domain | |||
NHEFJLLP_02620 | 4.1e-77 | S | NADPH-dependent FMN reductase | |||
NHEFJLLP_02621 | 2.8e-117 | S | Haloacid dehalogenase-like hydrolase | |||
NHEFJLLP_02622 | 6.6e-116 | |||||
NHEFJLLP_02623 | 3.1e-167 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_02624 | 3.1e-77 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
NHEFJLLP_02625 | 3.4e-227 | sip | L | Belongs to the 'phage' integrase family | ||
NHEFJLLP_02626 | 1.1e-06 | K | Cro/C1-type HTH DNA-binding domain | |||
NHEFJLLP_02628 | 1.6e-08 | |||||
NHEFJLLP_02629 | 6.8e-90 | L | DNA replication protein | |||
NHEFJLLP_02630 | 3.6e-31 | L | DNA replication protein | |||
NHEFJLLP_02631 | 2.2e-265 | S | Virulence-associated protein E | |||
NHEFJLLP_02632 | 4.5e-85 | |||||
NHEFJLLP_02633 | 2.6e-23 | |||||
NHEFJLLP_02634 | 3.7e-52 | S | head-tail joining protein | |||
NHEFJLLP_02635 | 1.8e-68 | L | HNH endonuclease | |||
NHEFJLLP_02636 | 3.6e-82 | terS | L | overlaps another CDS with the same product name | ||
NHEFJLLP_02637 | 0.0 | terL | S | overlaps another CDS with the same product name | ||
NHEFJLLP_02639 | 1.1e-198 | S | Phage portal protein | |||
NHEFJLLP_02640 | 7.9e-211 | S | Caudovirus prohead serine protease | |||
NHEFJLLP_02643 | 4.7e-39 | S | Phage gp6-like head-tail connector protein | |||
NHEFJLLP_02644 | 4.1e-49 | |||||
NHEFJLLP_02646 | 7.4e-94 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
NHEFJLLP_02647 | 1e-81 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
NHEFJLLP_02648 | 1.3e-193 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
NHEFJLLP_02649 | 3.5e-168 | S | Sterol carrier protein domain | |||
NHEFJLLP_02650 | 4.1e-108 | mltD | CBM50 | M | NlpC P60 family protein | |
NHEFJLLP_02651 | 1.7e-28 | |||||
NHEFJLLP_02652 | 1e-57 | yabA | L | Involved in initiation control of chromosome replication | ||
NHEFJLLP_02653 | 3.3e-186 | holB | 2.7.7.7 | L | DNA polymerase III | |
NHEFJLLP_02654 | 2.4e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
NHEFJLLP_02655 | 9.5e-18 | |||||
NHEFJLLP_02658 | 2.4e-97 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
NHEFJLLP_02660 | 2.9e-83 | mutR | K | sequence-specific DNA binding | ||
NHEFJLLP_02661 | 3.7e-151 | rlrG | K | Transcriptional regulator | ||
NHEFJLLP_02662 | 1.3e-76 | S | Conserved hypothetical protein 698 | |||
NHEFJLLP_02663 | 0.0 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
NHEFJLLP_02664 | 5.6e-26 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
NHEFJLLP_02665 | 2e-172 | ugpA | U | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_02666 | 4.5e-103 | P | ABC transporter | |||
NHEFJLLP_02667 | 6.8e-116 | P | cobalt transport | |||
NHEFJLLP_02668 | 5.7e-259 | S | ATPases associated with a variety of cellular activities | |||
NHEFJLLP_02669 | 8.5e-50 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NHEFJLLP_02670 | 3.5e-58 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NHEFJLLP_02672 | 4.5e-219 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NHEFJLLP_02673 | 4e-164 | FbpA | K | Domain of unknown function (DUF814) | ||
NHEFJLLP_02674 | 1.3e-60 | S | Domain of unknown function (DU1801) | |||
NHEFJLLP_02675 | 4.9e-34 | |||||
NHEFJLLP_02676 | 2e-144 | yghZ | C | Aldo keto reductase family protein | ||
NHEFJLLP_02677 | 1.1e-26 | yghZ | C | Aldo keto reductase family protein | ||
NHEFJLLP_02678 | 3e-113 | pgm1 | G | phosphoglycerate mutase | ||
NHEFJLLP_02679 | 9.2e-203 | 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 | |
NHEFJLLP_02680 | 2.3e-215 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NHEFJLLP_02681 | 2.6e-79 | yiaC | K | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_02682 | 8.6e-309 | oppA | E | ABC transporter, substratebinding protein | ||
NHEFJLLP_02684 | 3.5e-88 | S | AAA domain | |||
NHEFJLLP_02685 | 5.5e-252 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
NHEFJLLP_02686 | 4.2e-158 | amd | 3.5.1.47 | E | Peptidase family M20/M25/M40 | |
NHEFJLLP_02687 | 7.7e-163 | IQ | KR domain | |||
NHEFJLLP_02688 | 3.3e-65 | S | Protein of unknown function (DUF1093) | |||
NHEFJLLP_02689 | 3.8e-135 | yxkH | G | Polysaccharide deacetylase | ||
NHEFJLLP_02690 | 1.2e-103 | |||||
NHEFJLLP_02691 | 8.8e-243 | P | Major Facilitator Superfamily | |||
NHEFJLLP_02692 | 1.2e-46 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NHEFJLLP_02693 | 2.2e-87 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_02695 | 5.4e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
NHEFJLLP_02696 | 7.2e-228 | 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 | |
NHEFJLLP_02697 | 9.6e-85 | |||||
NHEFJLLP_02698 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
NHEFJLLP_02699 | 1e-189 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
NHEFJLLP_02700 | 5.1e-92 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
NHEFJLLP_02701 | 5.1e-148 | DegV | S | EDD domain protein, DegV family | ||
NHEFJLLP_02702 | 1.7e-150 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
NHEFJLLP_02703 | 9e-113 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
NHEFJLLP_02704 | 3.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
NHEFJLLP_02705 | 1.3e-260 | ctpA | 3.4.21.102 | M | Belongs to the peptidase S41A family | |
NHEFJLLP_02706 | 3.3e-251 | emrY | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02707 | 1.5e-197 | XK27_00915 | C | Luciferase-like monooxygenase | ||
NHEFJLLP_02708 | 1.9e-83 | |||||
NHEFJLLP_02709 | 1.5e-194 | pipD | E | Dipeptidase | ||
NHEFJLLP_02710 | 3e-40 | |||||
NHEFJLLP_02711 | 1.1e-71 | D | Alpha beta | |||
NHEFJLLP_02712 | 1.3e-201 | L | Transposase DDE domain | |||
NHEFJLLP_02713 | 6e-45 | L | Transposase DDE domain | |||
NHEFJLLP_02714 | 1.6e-143 | soj | D | AAA domain | ||
NHEFJLLP_02715 | 1.5e-33 | |||||
NHEFJLLP_02717 | 7e-26 | |||||
NHEFJLLP_02718 | 3.1e-101 | S | ABC transporter permease | |||
NHEFJLLP_02719 | 1.4e-234 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NHEFJLLP_02722 | 4.2e-20 | |||||
NHEFJLLP_02725 | 4.3e-222 | sip | L | Belongs to the 'phage' integrase family | ||
NHEFJLLP_02728 | 5.9e-09 | |||||
NHEFJLLP_02729 | 4.8e-08 | |||||
NHEFJLLP_02730 | 2e-141 | L | DNA replication protein | |||
NHEFJLLP_02731 | 2.1e-263 | S | Virulence-associated protein E | |||
NHEFJLLP_02732 | 2.7e-85 | |||||
NHEFJLLP_02733 | 2e-23 | |||||
NHEFJLLP_02734 | 1.4e-48 | S | head-tail joining protein | |||
NHEFJLLP_02735 | 1.8e-68 | L | HNH endonuclease | |||
NHEFJLLP_02736 | 3.6e-82 | terS | L | overlaps another CDS with the same product name | ||
NHEFJLLP_02737 | 6.9e-50 | terL | S | overlaps another CDS with the same product name | ||
NHEFJLLP_02738 | 2.7e-241 | terL | S | overlaps another CDS with the same product name | ||
NHEFJLLP_02740 | 6.1e-202 | S | Phage portal protein | |||
NHEFJLLP_02741 | 4.9e-274 | S | Caudovirus prohead serine protease | |||
NHEFJLLP_02744 | 4.7e-39 | S | Phage gp6-like head-tail connector protein | |||
NHEFJLLP_02745 | 5.3e-57 | |||||
NHEFJLLP_02747 | 2.6e-65 | cytX | U | Belongs to the purine-cytosine permease (2.A.39) family | ||
NHEFJLLP_02748 | 5.1e-136 | S | peptidase C26 | |||
NHEFJLLP_02749 | 1.2e-102 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
NHEFJLLP_02750 | 2.3e-63 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
NHEFJLLP_02751 | 5.4e-100 | L | hmm pf00665 | |||
NHEFJLLP_02752 | 2.7e-81 | L | Helix-turn-helix domain | |||
NHEFJLLP_02754 | 3.6e-13 | XK27_07075 | S | CAAX protease self-immunity | ||
NHEFJLLP_02755 | 3e-36 | M | O-Antigen ligase | |||
NHEFJLLP_02756 | 1.6e-126 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
NHEFJLLP_02757 | 1.3e-66 | |||||
NHEFJLLP_02758 | 1.1e-76 | |||||
NHEFJLLP_02759 | 4.8e-85 | |||||
NHEFJLLP_02760 | 3.9e-44 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
NHEFJLLP_02762 | 1.3e-243 | 1.11.2.4, 1.14.14.1 | C | Cytochrome P450 | ||
NHEFJLLP_02764 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
NHEFJLLP_02765 | 1e-119 | S | Repeat protein | |||
NHEFJLLP_02766 | 5.5e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
NHEFJLLP_02767 | 7.1e-267 | N | domain, Protein | |||
NHEFJLLP_02768 | 1.7e-193 | S | Bacterial protein of unknown function (DUF916) | |||
NHEFJLLP_02769 | 5.1e-120 | N | WxL domain surface cell wall-binding | |||
NHEFJLLP_02770 | 2.6e-115 | ktrA | P | domain protein | ||
NHEFJLLP_02771 | 1.3e-241 | ktrB | P | Potassium uptake protein | ||
NHEFJLLP_02772 | 6.9e-225 | 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 | |
NHEFJLLP_02773 | 1.9e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
NHEFJLLP_02774 | 7.1e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
NHEFJLLP_02775 | 1.8e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
NHEFJLLP_02776 | 4.6e-28 | |||||
NHEFJLLP_02777 | 5.6e-95 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
NHEFJLLP_02778 | 1.6e-188 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
NHEFJLLP_02779 | 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) | |
NHEFJLLP_02780 | 1.2e-86 | divIVA | D | DivIVA domain protein | ||
NHEFJLLP_02781 | 3.4e-146 | ylmH | S | S4 domain protein | ||
NHEFJLLP_02782 | 1.2e-36 | yggT | S | YGGT family | ||
NHEFJLLP_02783 | 3.3e-71 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
NHEFJLLP_02784 | 1.4e-229 | 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 | ||
NHEFJLLP_02785 | 5.5e-245 | 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 | ||
NHEFJLLP_02786 | 5.8e-163 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
NHEFJLLP_02787 | 1.5e-197 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
NHEFJLLP_02788 | 3.6e-260 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
NHEFJLLP_02789 | 8.3e-179 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
NHEFJLLP_02790 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
NHEFJLLP_02791 | 7.5e-54 | ftsL | D | Cell division protein FtsL | ||
NHEFJLLP_02792 | 3.6e-174 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
NHEFJLLP_02793 | 1.4e-77 | mraZ | K | Belongs to the MraZ family | ||
NHEFJLLP_02794 | 1.6e-61 | S | Protein of unknown function (DUF3397) | |||
NHEFJLLP_02795 | 4.2e-175 | corA | P | CorA-like Mg2+ transporter protein | ||
NHEFJLLP_02796 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
NHEFJLLP_02797 | 2.8e-91 | ymfF | S | Peptidase M16 inactive domain protein | ||
NHEFJLLP_02798 | 2.9e-251 | ymfH | S | Peptidase M16 | ||
NHEFJLLP_02799 | 4.8e-109 | ymfM | S | Helix-turn-helix domain | ||
NHEFJLLP_02800 | 3.7e-97 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
NHEFJLLP_02801 | 2.5e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
NHEFJLLP_02802 | 5e-191 | 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 | ||
NHEFJLLP_02803 | 2.1e-216 | rny | S | Endoribonuclease that initiates mRNA decay | ||
NHEFJLLP_02804 | 2.7e-154 | ymdB | S | YmdB-like protein | ||
NHEFJLLP_02805 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
NHEFJLLP_02806 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
NHEFJLLP_02807 | 2e-61 | K | Transcriptional regulator, HxlR family | |||
NHEFJLLP_02808 | 4.6e-211 | ytbD | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02809 | 4.7e-84 | L | PFAM Integrase catalytic region | |||
NHEFJLLP_02810 | 9.6e-161 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
NHEFJLLP_02811 | 1.9e-253 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_02812 | 3.9e-24 | |||||
NHEFJLLP_02813 | 6.9e-217 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NHEFJLLP_02814 | 2.1e-38 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_02815 | 1.2e-23 | S | Family of unknown function (DUF5388) | |||
NHEFJLLP_02816 | 1.6e-143 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
NHEFJLLP_02817 | 2e-44 | E | glutamate:sodium symporter activity | |||
NHEFJLLP_02818 | 1.3e-215 | 3.5.1.47 | E | Peptidase family M20/M25/M40 | ||
NHEFJLLP_02820 | 2.6e-12 | yjdF | S | Protein of unknown function (DUF2992) | ||
NHEFJLLP_02821 | 1e-244 | arpJ | P | ABC transporter permease | ||
NHEFJLLP_02823 | 9.8e-25 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NHEFJLLP_02825 | 0.0 | S | Pfam Methyltransferase | |||
NHEFJLLP_02826 | 6.7e-268 | tagE2 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHEFJLLP_02827 | 1.8e-297 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
NHEFJLLP_02828 | 4.2e-29 | |||||
NHEFJLLP_02829 | 1.2e-94 | ytqB | 2.1.1.176 | J | Putative rRNA methylase | |
NHEFJLLP_02830 | 8.8e-124 | 3.6.1.27 | I | Acid phosphatase homologues | ||
NHEFJLLP_02831 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NHEFJLLP_02832 | 3e-301 | ytgP | S | Polysaccharide biosynthesis protein | ||
NHEFJLLP_02833 | 6.7e-136 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NHEFJLLP_02834 | 2.4e-150 | 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 | |
NHEFJLLP_02835 | 3.6e-18 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
NHEFJLLP_02836 | 1.2e-68 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
NHEFJLLP_02837 | 4.1e-57 | mngB | 3.2.1.170, 3.2.1.24 | GH38 | G | Glycosyl hydrolases family 38 N-terminal domain |
NHEFJLLP_02838 | 2.6e-39 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_02839 | 2.3e-151 | gntR | K | rpiR family | ||
NHEFJLLP_02840 | 2.2e-26 | N | Cell shape-determining protein MreB | |||
NHEFJLLP_02841 | 5e-69 | O | OsmC-like protein | |||
NHEFJLLP_02842 | 5.8e-46 | |||||
NHEFJLLP_02843 | 6.1e-97 | yfnA | E | Amino Acid | ||
NHEFJLLP_02844 | 1.4e-53 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NHEFJLLP_02845 | 1.1e-95 | K | Transcriptional regulator (TetR family) | |||
NHEFJLLP_02846 | 1.1e-37 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NHEFJLLP_02847 | 2.5e-150 | gntR | K | rpiR family | ||
NHEFJLLP_02849 | 3.8e-98 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
NHEFJLLP_02850 | 4.6e-11 | |||||
NHEFJLLP_02851 | 3.8e-99 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
NHEFJLLP_02852 | 1.5e-135 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
NHEFJLLP_02853 | 0.0 | typA | T | GTP-binding protein TypA | ||
NHEFJLLP_02854 | 6.3e-137 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
NHEFJLLP_02855 | 3.3e-46 | yktA | S | Belongs to the UPF0223 family | ||
NHEFJLLP_02856 | 4.1e-163 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
NHEFJLLP_02857 | 1.2e-266 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
NHEFJLLP_02858 | 6.8e-208 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
NHEFJLLP_02859 | 4.5e-180 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
NHEFJLLP_02860 | 1.6e-210 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
NHEFJLLP_02861 | 3.1e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
NHEFJLLP_02862 | 3.7e-85 | |||||
NHEFJLLP_02863 | 3.1e-33 | ykzG | S | Belongs to the UPF0356 family | ||
NHEFJLLP_02864 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
NHEFJLLP_02865 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
NHEFJLLP_02866 | 1.7e-75 | |||||
NHEFJLLP_02867 | 3.3e-49 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
NHEFJLLP_02868 | 4e-179 | mesE | M | Transport protein ComB | ||
NHEFJLLP_02869 | 5.6e-80 | 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 | |
NHEFJLLP_02870 | 3e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
NHEFJLLP_02871 | 1.1e-65 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
NHEFJLLP_02872 | 5.6e-141 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NHEFJLLP_02874 | 1.1e-83 | |||||
NHEFJLLP_02875 | 2.8e-85 | yvbK | 3.1.3.25 | K | GNAT family | |
NHEFJLLP_02876 | 3.2e-37 | |||||
NHEFJLLP_02877 | 5.2e-36 | S | pyridoxamine 5-phosphate | |||
NHEFJLLP_02878 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
NHEFJLLP_02879 | 4.8e-179 | 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 | |
NHEFJLLP_02880 | 1.7e-134 | 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 | |
NHEFJLLP_02881 | 2.5e-166 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
NHEFJLLP_02882 | 3.5e-174 | K | Transcriptional regulator, LysR family | |||
NHEFJLLP_02883 | 1.2e-219 | ydiN | EGP | Major Facilitator Superfamily | ||
NHEFJLLP_02884 | 5e-162 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
NHEFJLLP_02885 | 9.4e-161 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
NHEFJLLP_02886 | 1e-156 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NHEFJLLP_02887 | 2.3e-164 | G | Xylose isomerase-like TIM barrel | |||
NHEFJLLP_02888 | 4.7e-168 | K | Transcriptional regulator, LysR family | |||
NHEFJLLP_02889 | 3.3e-80 | yueI | S | Protein of unknown function (DUF1694) | ||
NHEFJLLP_02890 | 3.1e-110 | S | Protein of unknown function (DUF1648) | |||
NHEFJLLP_02891 | 3.3e-43 | czrA | K | Helix-turn-helix domain | ||
NHEFJLLP_02892 | 1.9e-40 | S | Cell surface protein | |||
NHEFJLLP_02894 | 1.6e-18 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_02895 | 5.4e-30 | 5.3.3.19 | S | Cupin 2, conserved barrel domain protein | ||
NHEFJLLP_02896 | 2.5e-53 | S | Cupin domain | |||
NHEFJLLP_02897 | 1.1e-166 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
NHEFJLLP_02898 | 9.1e-89 | |||||
NHEFJLLP_02899 | 2.9e-126 | epsB | M | biosynthesis protein | ||
NHEFJLLP_02900 | 2.4e-133 | amtB | P | ammonium transporter | ||
NHEFJLLP_02901 | 3.4e-80 | P | Major Facilitator Superfamily | |||
NHEFJLLP_02902 | 3.5e-36 | |||||
NHEFJLLP_02903 | 3.1e-14 | |||||
NHEFJLLP_02904 | 6.5e-41 | S | transglycosylase associated protein | |||
NHEFJLLP_02905 | 4.8e-29 | S | CsbD-like | |||
NHEFJLLP_02906 | 1.7e-254 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
NHEFJLLP_02907 | 1.6e-249 | 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 | |
NHEFJLLP_02908 | 1.2e-137 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
NHEFJLLP_02909 | 8.1e-224 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
NHEFJLLP_02910 | 2.6e-191 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NHEFJLLP_02911 | 7.3e-189 | cggR | K | Putative sugar-binding domain | ||
NHEFJLLP_02912 | 7.8e-244 | rpoN | K | Sigma-54 factor, core binding domain | ||
NHEFJLLP_02914 | 3e-102 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
NHEFJLLP_02915 | 1e-176 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
NHEFJLLP_02916 | 1.2e-305 | oppA | E | ABC transporter, substratebinding protein | ||
NHEFJLLP_02917 | 3.7e-168 | whiA | K | May be required for sporulation | ||
NHEFJLLP_02918 | 1.8e-147 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
NHEFJLLP_02919 | 6.6e-96 | |||||
NHEFJLLP_02920 | 2e-62 | |||||
NHEFJLLP_02921 | 7.2e-107 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | Belongs to the TrpF family | |
NHEFJLLP_02924 | 8.9e-42 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_02925 | 9.7e-86 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NHEFJLLP_02927 | 2.4e-22 | plnF | ||||
NHEFJLLP_02928 | 6.3e-129 | S | CAAX protease self-immunity | |||
NHEFJLLP_02929 | 2.3e-153 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
NHEFJLLP_02930 | 1e-40 | |||||
NHEFJLLP_02931 | 9.7e-253 | ydiC1 | EGP | Major facilitator Superfamily | ||
NHEFJLLP_02932 | 3.3e-65 | K | helix_turn_helix, mercury resistance | |||
NHEFJLLP_02933 | 2.3e-251 | T | PhoQ Sensor | |||
NHEFJLLP_02934 | 6.4e-128 | K | Transcriptional regulatory protein, C terminal | |||
NHEFJLLP_02935 | 1.8e-49 | |||||
NHEFJLLP_02936 | 2.1e-129 | yidA | K | Helix-turn-helix domain, rpiR family | ||
NHEFJLLP_02937 | 3.9e-243 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_02938 | 9.9e-57 | |||||
NHEFJLLP_02939 | 2.1e-41 | |||||
NHEFJLLP_02940 | 5.4e-184 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NHEFJLLP_02941 | 2e-258 | loxD | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
NHEFJLLP_02942 | 1.3e-47 | |||||
NHEFJLLP_02943 | 2.7e-123 | 2.7.6.5 | S | RelA SpoT domain protein | ||
NHEFJLLP_02944 | 3.1e-104 | K | transcriptional regulator | |||
NHEFJLLP_02945 | 2.4e-147 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
NHEFJLLP_02946 | 1.7e-75 | K | Transcriptional regulator | |||
NHEFJLLP_02948 | 9.8e-129 | fhuC | 3.6.3.35 | P | ABC transporter | |
NHEFJLLP_02949 | 2.2e-48 | S | GyrI-like small molecule binding domain | |||
NHEFJLLP_02950 | 3.8e-69 | S | Iron-sulphur cluster biosynthesis | |||
NHEFJLLP_02952 | 6.4e-44 | mltD | CBM50 | M | PFAM NLP P60 protein | |
NHEFJLLP_02953 | 1.2e-72 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
NHEFJLLP_02954 | 1e-41 | |||||
NHEFJLLP_02955 | 1.4e-71 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
NHEFJLLP_02956 | 9.5e-49 | mltD | CBM50 | M | PFAM NLP P60 protein | |
NHEFJLLP_02957 | 1.8e-34 | potB | P | ABC transporter permease | ||
NHEFJLLP_02958 | 3.8e-140 | potC | P | ABC transporter permease | ||
NHEFJLLP_02959 | 1.6e-39 | potB | P | ABC transporter permease | ||
NHEFJLLP_02960 | 2.9e-140 | potC | P | ABC transporter permease | ||
NHEFJLLP_02961 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
NHEFJLLP_02962 | 9.5e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
NHEFJLLP_02963 | 8.4e-137 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
NHEFJLLP_02964 | 1.8e-147 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
NHEFJLLP_02965 | 2.5e-82 | 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 | ||
NHEFJLLP_02966 | 2.2e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
NHEFJLLP_02967 | 1.3e-151 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
NHEFJLLP_02968 | 6.5e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
NHEFJLLP_02969 | 4.7e-134 | S | Haloacid dehalogenase-like hydrolase | |||
NHEFJLLP_02970 | 2.3e-187 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NHEFJLLP_02971 | 1.8e-39 | yazA | L | GIY-YIG catalytic domain protein | ||
NHEFJLLP_02972 | 4.6e-132 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
NHEFJLLP_02973 | 6.4e-119 | plsC | 2.3.1.51 | I | Acyltransferase | |
NHEFJLLP_02974 | 4.3e-33 | yneF | S | Uncharacterised protein family (UPF0154) | ||
NHEFJLLP_02975 | 2.9e-36 | ynzC | S | UPF0291 protein | ||
NHEFJLLP_02976 | 5.6e-115 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
NHEFJLLP_02977 | 9.7e-24 | lytE | M | LysM domain | ||
NHEFJLLP_02978 | 3.7e-44 | |||||
NHEFJLLP_02979 | 1.5e-100 | zmp1 | O | Zinc-dependent metalloprotease | ||
NHEFJLLP_02980 | 4.2e-186 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
NHEFJLLP_02981 | 4.8e-187 | |||||
NHEFJLLP_02982 | 1.2e-76 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
NHEFJLLP_02983 | 4.3e-77 | K | Transcriptional regulator | |||
NHEFJLLP_02984 | 1.4e-136 | S | response to antibiotic | |||
NHEFJLLP_02985 | 3.4e-132 | K | UTRA domain | |||
NHEFJLLP_02986 | 2.5e-58 | estA | S | Putative esterase | ||
NHEFJLLP_02987 | 1.2e-73 | 1.5.1.3 | H | RibD C-terminal domain | ||
NHEFJLLP_02988 | 5e-141 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NHEFJLLP_02989 | 1.2e-124 | epsB | M | biosynthesis protein | ||
NHEFJLLP_02990 | 1.8e-75 | repC | L | Initiator Replication protein | ||
NHEFJLLP_02991 | 1.1e-28 | |||||
NHEFJLLP_02994 | 1.2e-74 | S | Plasmid replication protein | |||
NHEFJLLP_02997 | 2e-25 | L | PFAM Integrase catalytic region | |||
NHEFJLLP_02998 | 1.6e-22 | |||||
NHEFJLLP_03001 | 3.7e-100 | vrlS | L | helicase superfamily c-terminal domain | ||
NHEFJLLP_03003 | 7e-17 | vrlR | S | Domain of unknown function (DUF1837) | ||
NHEFJLLP_03005 | 1.6e-61 | |||||
NHEFJLLP_03007 | 2.6e-65 | |||||
NHEFJLLP_03008 | 1.4e-110 | pgm8 | G | Histidine phosphatase superfamily (branch 1) | ||
NHEFJLLP_03009 | 8.1e-91 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_03010 | 2.6e-82 | S | Protein of unknown function (DUF3021) | |||
NHEFJLLP_03011 | 6e-73 | hsp1 | O | Belongs to the small heat shock protein (HSP20) family | ||
NHEFJLLP_03012 | 4.7e-79 | uspA | T | universal stress protein | ||
NHEFJLLP_03013 | 3.2e-61 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_03014 | 1.4e-17 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
NHEFJLLP_03015 | 2.1e-40 | K | Helix-turn-helix domain | |||
NHEFJLLP_03016 | 1.7e-148 | cof | S | haloacid dehalogenase-like hydrolase | ||
NHEFJLLP_03017 | 4.1e-153 | qorB | 1.6.5.2 | GM | NmrA-like family | |
NHEFJLLP_03018 | 9.4e-77 | |||||
NHEFJLLP_03019 | 4.2e-275 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NHEFJLLP_03020 | 1.4e-116 | ybbL | S | ABC transporter, ATP-binding protein | ||
NHEFJLLP_03021 | 6.8e-128 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
NHEFJLLP_03022 | 2.6e-205 | S | DUF218 domain | |||
NHEFJLLP_03023 | 1.4e-181 | 5.1.1.1 | K | Periplasmic binding proteins and sugar binding domain of LacI family | ||
NHEFJLLP_03024 | 0.0 | malA | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
NHEFJLLP_03025 | 0.0 | scrA | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
NHEFJLLP_03026 | 3.2e-127 | S | Putative adhesin | |||
NHEFJLLP_03027 | 7.7e-72 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
NHEFJLLP_03028 | 2.3e-173 | L | restriction endonuclease | |||
NHEFJLLP_03029 | 1.9e-39 | K | transcriptional regulator, MerR family | |||
NHEFJLLP_03030 | 2.5e-49 | XK27_04080 | H | RibD C-terminal domain | ||
NHEFJLLP_03032 | 6.8e-45 | mleP3 | S | Membrane transport protein | ||
NHEFJLLP_03033 | 3.5e-109 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
NHEFJLLP_03034 | 2.1e-100 | aspA | 4.2.1.2, 4.3.1.1 | E | Fumarase C C-terminus | |
NHEFJLLP_03035 | 1e-45 | mleP3 | S | Membrane transport protein | ||
NHEFJLLP_03036 | 1.6e-129 | ybbR | S | YbbR-like protein | ||
NHEFJLLP_03037 | 2.4e-97 | acuB | S | Domain in cystathionine beta-synthase and other proteins. | ||
NHEFJLLP_03038 | 3.3e-124 | livF | E | ABC transporter | ||
NHEFJLLP_03039 | 1.8e-139 | livG | E | Branched-chain amino acid ATP-binding cassette transporter | ||
NHEFJLLP_03040 | 7.6e-140 | livM | E | Branched-chain amino acid transport system / permease component | ||
NHEFJLLP_03041 | 1.9e-153 | livH | U | Branched-chain amino acid transport system / permease component | ||
NHEFJLLP_03042 | 1.2e-211 | livJ | E | Receptor family ligand binding region | ||
NHEFJLLP_03044 | 7e-33 | |||||
NHEFJLLP_03045 | 3.5e-114 | zmp3 | O | Zinc-dependent metalloprotease | ||
NHEFJLLP_03046 | 2.8e-82 | gtrA | S | GtrA-like protein | ||
NHEFJLLP_03047 | 2.1e-122 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_03048 | 4.1e-284 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
NHEFJLLP_03049 | 6.8e-72 | T | Belongs to the universal stress protein A family | |||
NHEFJLLP_03050 | 1.1e-46 | |||||
NHEFJLLP_03051 | 1.9e-116 | S | SNARE associated Golgi protein | |||
NHEFJLLP_03052 | 1.9e-47 | K | Transcriptional regulator, ArsR family | |||
NHEFJLLP_03053 | 1.2e-95 | cadD | P | Cadmium resistance transporter | ||
NHEFJLLP_03054 | 2.3e-54 | azlD | S | branched-chain amino acid | ||
NHEFJLLP_03055 | 2.6e-71 | azlC | E | branched-chain amino acid | ||
NHEFJLLP_03056 | 1.7e-24 | L | Transposase and inactivated derivatives | |||
NHEFJLLP_03057 | 8.5e-53 | phnT | 3.6.3.30 | P | ATPases associated with a variety of cellular activities | |
NHEFJLLP_03058 | 5.8e-70 | frataxin | S | Domain of unknown function (DU1801) | ||
NHEFJLLP_03059 | 6.5e-110 | pgm5 | G | Phosphoglycerate mutase family | ||
NHEFJLLP_03060 | 3e-47 | ywnB | S | NAD(P)H-binding | ||
NHEFJLLP_03061 | 3.2e-40 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
NHEFJLLP_03062 | 8.5e-41 | |||||
NHEFJLLP_03063 | 4.1e-32 | L | leucine-zipper of insertion element IS481 | |||
NHEFJLLP_03064 | 1.4e-86 | ecsA_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
NHEFJLLP_03065 | 6.3e-122 | yfeX | P | Peroxidase | ||
NHEFJLLP_03066 | 7.7e-166 | mleR | K | LysR substrate binding domain | ||
NHEFJLLP_03067 | 0.0 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
NHEFJLLP_03068 | 1.1e-217 | nhaC | C | Na H antiporter NhaC | ||
NHEFJLLP_03069 | 6.5e-165 | 3.5.1.10 | C | nadph quinone reductase | ||
NHEFJLLP_03070 | 0.0 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
NHEFJLLP_03071 | 9.1e-173 | scrR | K | Transcriptional regulator, LacI family | ||
NHEFJLLP_03072 | 1.3e-303 | scrB | 3.2.1.26 | GH32 | G | invertase |
NHEFJLLP_03073 | 0.0 | scrA | 2.7.1.193, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
NHEFJLLP_03074 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
NHEFJLLP_03075 | 1.8e-169 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
NHEFJLLP_03076 | 2e-45 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
NHEFJLLP_03077 | 4.5e-241 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
NHEFJLLP_03078 | 1e-232 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
NHEFJLLP_03079 | 7.8e-58 | 3.2.1.96 | G | Glycosyl hydrolase family 85 | ||
NHEFJLLP_03080 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
NHEFJLLP_03081 | 4e-209 | msmK | P | Belongs to the ABC transporter superfamily | ||
NHEFJLLP_03082 | 2e-260 | malS | 3.2.1.1 | GH13 | G | Glycogen debranching enzyme, glucanotransferase domain |
NHEFJLLP_03083 | 5.3e-150 | malA | S | maltodextrose utilization protein MalA | ||
NHEFJLLP_03084 | 1.4e-161 | malD | P | ABC transporter permease | ||
NHEFJLLP_03085 | 2.2e-227 | malC | P | Binding-protein-dependent transport system inner membrane component | ||
NHEFJLLP_03086 | 4.2e-231 | mdxE | G | Bacterial extracellular solute-binding protein | ||
NHEFJLLP_03087 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
NHEFJLLP_03088 | 2e-180 | yvdE | K | helix_turn _helix lactose operon repressor | ||
NHEFJLLP_03089 | 1e-190 | malR | K | Transcriptional regulator, LacI family | ||
NHEFJLLP_03090 | 8.6e-133 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_03091 | 2e-56 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
NHEFJLLP_03092 | 1.9e-101 | dhaL | 2.7.1.121 | S | Dak2 | |
NHEFJLLP_03093 | 2.9e-145 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
NHEFJLLP_03094 | 2.2e-66 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
NHEFJLLP_03095 | 1.1e-211 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
NHEFJLLP_03096 | 1.5e-146 | S | hydrolase activity, acting on ester bonds | |||
NHEFJLLP_03097 | 1.1e-192 | |||||
NHEFJLLP_03098 | 3.3e-121 | 3.6.3.35 | P | ATPases associated with a variety of cellular activities | ||
NHEFJLLP_03099 | 1.3e-123 | |||||
NHEFJLLP_03100 | 6.2e-182 | mccF | 3.4.17.13 | V | LD-carboxypeptidase | |
NHEFJLLP_03101 | 2.6e-239 | M | hydrolase, family 25 | |||
NHEFJLLP_03102 | 1.4e-78 | K | Acetyltransferase (GNAT) domain | |||
NHEFJLLP_03103 | 5.1e-209 | mccF | V | LD-carboxypeptidase | ||
NHEFJLLP_03104 | 2.8e-241 | M | Glycosyltransferase, group 2 family protein | |||
NHEFJLLP_03105 | 1.2e-73 | S | SnoaL-like domain | |||
NHEFJLLP_03106 | 2.8e-145 | yjfP | S | COG1073 Hydrolases of the alpha beta superfamily | ||
NHEFJLLP_03107 | 1.8e-218 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NHEFJLLP_03108 | 6.8e-218 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NHEFJLLP_03109 | 8.3e-109 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_03110 | 5e-120 | draG | 3.2.2.24 | O | ADP-ribosylglycohydrolase | |
NHEFJLLP_03111 | 1.1e-96 | S | CAAX protease self-immunity | |||
NHEFJLLP_03112 | 1.8e-30 | |||||
NHEFJLLP_03113 | 2.4e-40 | helD | 3.6.4.12 | L | DNA helicase | |
NHEFJLLP_03114 | 6.1e-76 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
NHEFJLLP_03117 | 3e-81 | K | sequence-specific DNA binding | |||
NHEFJLLP_03121 | 8.4e-17 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
NHEFJLLP_03122 | 1.9e-214 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
NHEFJLLP_03123 | 6.4e-257 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
NHEFJLLP_03124 | 3e-262 | frdC | 1.3.5.4 | C | FAD binding domain | |
NHEFJLLP_03125 | 1.2e-94 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
NHEFJLLP_03126 | 4.9e-162 | mleR | K | LysR family transcriptional regulator | ||
NHEFJLLP_03127 | 1.8e-167 | mleR | K | LysR family | ||
NHEFJLLP_03128 | 2.8e-307 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
NHEFJLLP_03129 | 2.2e-147 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
NHEFJLLP_03130 | 3.3e-38 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_03131 | 9.3e-36 | K | Helix-turn-helix domain | |||
NHEFJLLP_03132 | 2.9e-93 | 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 | |
NHEFJLLP_03133 | 4e-30 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
NHEFJLLP_03134 | 1.2e-51 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_03135 | 3.4e-48 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
NHEFJLLP_03136 | 2.6e-23 | |||||
NHEFJLLP_03139 | 6.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
NHEFJLLP_03140 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
NHEFJLLP_03141 | 1.4e-67 | rplI | J | Binds to the 23S rRNA | ||
NHEFJLLP_03142 | 7.8e-242 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
NHEFJLLP_03143 | 8.8e-226 | yttB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_03144 | 1e-142 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
NHEFJLLP_03145 | 5.6e-228 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
NHEFJLLP_03146 | 4.2e-276 | E | ABC transporter, substratebinding protein | |||
NHEFJLLP_03147 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
NHEFJLLP_03148 | 1.4e-94 | M | ErfK YbiS YcfS YnhG | |||
NHEFJLLP_03149 | 2.6e-70 | asnB | 6.3.5.4 | E | Asparagine synthase | |
NHEFJLLP_03150 | 8.4e-31 | 3.4.13.21, 3.4.15.6 | E | Belongs to the peptidase S51 family | ||
NHEFJLLP_03151 | 3.9e-226 | uvrA3 | L | excinuclease ABC | ||
NHEFJLLP_03152 | 1e-37 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
NHEFJLLP_03153 | 8e-33 | L | hmm pf00665 | |||
NHEFJLLP_03154 | 1.6e-45 | L | hmm pf00665 | |||
NHEFJLLP_03159 | 5.1e-08 | |||||
NHEFJLLP_03165 | 5.4e-19 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
NHEFJLLP_03166 | 4.6e-40 | GT89 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | ||
NHEFJLLP_03167 | 5.1e-153 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
NHEFJLLP_03168 | 2.4e-65 | GM | NmrA-like family | |||
NHEFJLLP_03169 | 4.1e-106 | ygaC | J | Belongs to the UPF0374 family | ||
NHEFJLLP_03170 | 8.1e-13 | cwlO | M | NlpC/P60 family | ||
NHEFJLLP_03171 | 2.5e-16 | |||||
NHEFJLLP_03172 | 9.2e-47 | |||||
NHEFJLLP_03174 | 3.2e-161 | dnaC | L | IstB-like ATP binding protein | ||
NHEFJLLP_03175 | 1.2e-69 | L | DnaD domain protein | |||
NHEFJLLP_03186 | 5.7e-26 | S | Domain of unknown function (DUF1883) | |||
NHEFJLLP_03188 | 2.2e-94 | kilA | K | BRO family, N-terminal domain | ||
NHEFJLLP_03190 | 1.2e-25 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
NHEFJLLP_03191 | 1.5e-36 | S | Pfam:Peptidase_M78 | |||
NHEFJLLP_03192 | 4.8e-57 | dinG | 2.7.7.7, 3.6.4.12 | L | DNA-directed DNA polymerase activity | |
NHEFJLLP_03194 | 5.3e-23 | |||||
NHEFJLLP_03199 | 3.4e-54 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_03200 | 1.1e-62 | GM | NmrA-like family | |||
NHEFJLLP_03201 | 5.1e-63 | isp | L | Transposase | ||
NHEFJLLP_03202 | 5.4e-120 | drrB | U | ABC-2 type transporter | ||
NHEFJLLP_03203 | 1.1e-98 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
NHEFJLLP_03204 | 5.2e-33 | 3.4.21.72 | M | Bacterial Ig-like domain (group 3) | ||
NHEFJLLP_03205 | 8.7e-90 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
NHEFJLLP_03206 | 2e-135 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
NHEFJLLP_03207 | 1.4e-95 | D | Cellulose biosynthesis protein BcsQ | |||
NHEFJLLP_03208 | 6.4e-26 | |||||
NHEFJLLP_03209 | 2.6e-236 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
NHEFJLLP_03210 | 5.8e-36 | |||||
NHEFJLLP_03211 | 1.4e-31 | |||||
NHEFJLLP_03212 | 1.3e-46 | KLT | serine threonine protein kinase | |||
NHEFJLLP_03213 | 8.8e-106 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_03215 | 4e-146 | U | TraM recognition site of TraD and TraG | |||
NHEFJLLP_03216 | 3.9e-07 | ligA | 6.5.1.2 | L | BRCA1 C Terminus (BRCT) domain | |
NHEFJLLP_03219 | 6.6e-53 | S | Protein of unknown function (DUF975) | |||
NHEFJLLP_03220 | 6.2e-94 | tnpR1 | L | Resolvase, N terminal domain | ||
NHEFJLLP_03221 | 2.2e-19 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NHEFJLLP_03222 | 1e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_03223 | 9.5e-208 | mtnE | 2.6.1.83 | E | Aminotransferase | |
NHEFJLLP_03224 | 1.6e-31 | |||||
NHEFJLLP_03225 | 2.7e-134 | Q | Methyltransferase | |||
NHEFJLLP_03226 | 4e-122 | treB | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
NHEFJLLP_03227 | 1.3e-124 | S | Fic/DOC family | |||
NHEFJLLP_03228 | 6.5e-58 | |||||
NHEFJLLP_03229 | 7.2e-115 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
NHEFJLLP_03230 | 3.2e-115 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
NHEFJLLP_03231 | 1.2e-56 | |||||
NHEFJLLP_03239 | 6.9e-78 | ctsR | K | Belongs to the CtsR family | ||
NHEFJLLP_03240 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
NHEFJLLP_03241 | 1.5e-109 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_03242 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NHEFJLLP_03243 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NHEFJLLP_03244 | 4.8e-34 | |||||
NHEFJLLP_03245 | 2.8e-58 | chpA | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
NHEFJLLP_03246 | 4.8e-196 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
NHEFJLLP_03247 | 1.8e-84 | pts29C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NHEFJLLP_03248 | 4.6e-51 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
NHEFJLLP_03249 | 1.2e-57 | K | Transcriptional regulator PadR-like family | |||
NHEFJLLP_03250 | 6.2e-165 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
NHEFJLLP_03251 | 5.4e-153 | nanK | GK | ROK family | ||
NHEFJLLP_03252 | 6.2e-134 | kguE | 2.7.1.45 | G | Xylose isomerase domain protein TIM barrel | |
NHEFJLLP_03253 | 5.2e-207 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NHEFJLLP_03254 | 1.7e-271 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
NHEFJLLP_03255 | 6.3e-159 | I | alpha/beta hydrolase fold | |||
NHEFJLLP_03256 | 2.9e-164 | I | alpha/beta hydrolase fold | |||
NHEFJLLP_03257 | 3.7e-72 | yueI | S | Protein of unknown function (DUF1694) | ||
NHEFJLLP_03258 | 7.4e-136 | K | Helix-turn-helix domain, rpiR family | |||
NHEFJLLP_03259 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
NHEFJLLP_03260 | 7e-112 | K | DeoR C terminal sensor domain | |||
NHEFJLLP_03261 | 3.2e-18 | 2.7.13.3 | T | GHKL domain | ||
NHEFJLLP_03262 | 7.6e-105 | kup | P | Transport of potassium into the cell | ||
NHEFJLLP_03266 | 8.7e-292 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NHEFJLLP_03267 | 1.1e-189 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
NHEFJLLP_03268 | 1.2e-163 | 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 | ||
NHEFJLLP_03269 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
NHEFJLLP_03270 | 1.7e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NHEFJLLP_03271 | 5.5e-253 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
NHEFJLLP_03272 | 3.1e-74 | yabR | J | RNA binding | ||
NHEFJLLP_03273 | 1.1e-63 | divIC | D | Septum formation initiator | ||
NHEFJLLP_03275 | 2.2e-42 | yabO | J | S4 domain protein | ||
NHEFJLLP_03276 | 3.3e-289 | yabM | S | Polysaccharide biosynthesis protein | ||
NHEFJLLP_03277 | 8.1e-123 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
NHEFJLLP_03278 | 2.8e-102 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NHEFJLLP_03280 | 7.5e-98 | S | CAAX protease self-immunity | |||
NHEFJLLP_03281 | 1.4e-144 | |||||
NHEFJLLP_03282 | 1.4e-175 | L | Integrase core domain | |||
NHEFJLLP_03283 | 3.3e-26 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
NHEFJLLP_03285 | 4.6e-39 | L | Transposase | |||
NHEFJLLP_03286 | 1.5e-147 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
NHEFJLLP_03287 | 1.3e-90 | ymdB | S | Macro domain protein | ||
NHEFJLLP_03288 | 1.2e-95 | K | transcriptional regulator | |||
NHEFJLLP_03289 | 5.5e-50 | yvlA | ||||
NHEFJLLP_03290 | 6e-161 | ypuA | S | Protein of unknown function (DUF1002) | ||
NHEFJLLP_03291 | 0.0 | |||||
NHEFJLLP_03292 | 9.8e-186 | S | Bacterial protein of unknown function (DUF916) | |||
NHEFJLLP_03293 | 1.7e-129 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_03294 | 6.7e-136 | T | Response regulator containing CheY-like receiver domain and AraC-type DNA-binding domain | |||
NHEFJLLP_03295 | 3.5e-88 | K | Winged helix DNA-binding domain | |||
NHEFJLLP_03296 | 2.4e-116 | luxT | K | Bacterial regulatory proteins, tetR family | ||
NHEFJLLP_03297 | 1.8e-119 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
NHEFJLLP_03298 | 2.7e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
NHEFJLLP_03299 | 1.6e-70 | |||||
NHEFJLLP_03300 | 5.9e-100 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
NHEFJLLP_03301 | 1.8e-44 | |||||
NHEFJLLP_03302 | 1.2e-177 | K | LysR substrate binding domain | |||
NHEFJLLP_03303 | 2.1e-111 | 1.3.5.4 | S | NADPH-dependent FMN reductase | ||
NHEFJLLP_03304 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
NHEFJLLP_03305 | 1.7e-99 | |||||
NHEFJLLP_03306 | 1.6e-76 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
NHEFJLLP_03307 | 6.1e-185 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
NHEFJLLP_03308 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
NHEFJLLP_03309 | 1.7e-19 | S | NUDIX domain | |||
NHEFJLLP_03310 | 0.0 | S | membrane | |||
NHEFJLLP_03311 | 2.1e-114 | S | (CBS) domain | |||
NHEFJLLP_03312 | 2.6e-48 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
NHEFJLLP_03313 | 3.1e-44 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
NHEFJLLP_03314 | 2e-75 | S | Domain of unknown function (DUF4811) | |||
NHEFJLLP_03315 | 5.4e-58 | rimL | J | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_03316 | 4.6e-41 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
NHEFJLLP_03318 | 5.3e-45 | K | MarR family | |||
NHEFJLLP_03319 | 5.8e-81 | P | Cation efflux family | |||
NHEFJLLP_03320 | 4e-17 | ybbK | S | Protein of unknown function (DUF523) | ||
NHEFJLLP_03322 | 1.6e-51 | ypaH | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
NHEFJLLP_03323 | 1.7e-10 | rmaI | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_03324 | 2.2e-15 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_03326 | 5.4e-133 | IQ | Dehydrogenase reductase | |||
NHEFJLLP_03327 | 3.4e-54 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_03328 | 4.3e-50 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_03329 | 8.7e-109 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
NHEFJLLP_03330 | 2e-171 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
NHEFJLLP_03331 | 5.6e-55 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_03332 | 3e-91 | IQ | reductase | |||
NHEFJLLP_03333 | 4.1e-48 | yvkB | K | Bacterial regulatory proteins, tetR family | ||
NHEFJLLP_03334 | 1.5e-92 | S | ABC-2 family transporter protein | |||
NHEFJLLP_03335 | 6.2e-102 | lrgB | M | LrgB-like family | ||
NHEFJLLP_03336 | 7.5e-40 | lrgA | S | LrgA family | ||
NHEFJLLP_03337 | 3.7e-83 | lytT | K | response regulator receiver | ||
NHEFJLLP_03338 | 1.9e-250 | lytS | 2.7.13.3 | T | LytS YhcK-type transmembrane receptor domain protein | |
NHEFJLLP_03339 | 7.2e-32 | yvaC | S | Fusaric acid resistance protein-like | ||
NHEFJLLP_03340 | 6.2e-45 | K | helix_turn_helix, arabinose operon control protein | |||
NHEFJLLP_03341 | 6.1e-115 | blt5 | EGP | Major facilitator Superfamily | ||
NHEFJLLP_03342 | 4.5e-114 | C | COG0277 FAD FMN-containing dehydrogenases | |||
NHEFJLLP_03345 | 3e-20 | K | Cro/C1-type HTH DNA-binding domain | |||
NHEFJLLP_03347 | 3.4e-44 | K | Transcriptional regulator PadR-like family | |||
NHEFJLLP_03348 | 7.7e-149 | ORF00048 | ||||
NHEFJLLP_03349 | 2.3e-214 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_03350 | 1.6e-112 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NHEFJLLP_03351 | 7.8e-200 | 3.3.1.1 | H | adenosylhomocysteinase activity | ||
NHEFJLLP_03352 | 1.1e-125 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_03354 | 0.0 | acm2 | 3.2.1.17 | NU | Bacterial SH3 domain | |
NHEFJLLP_03355 | 5.1e-195 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
NHEFJLLP_03356 | 4e-60 | |||||
NHEFJLLP_03357 | 1.7e-73 | |||||
NHEFJLLP_03358 | 5e-82 | yybC | S | Protein of unknown function (DUF2798) | ||
NHEFJLLP_03359 | 6.3e-45 | |||||
NHEFJLLP_03360 | 5.2e-47 | |||||
NHEFJLLP_03361 | 9.3e-206 | metB | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
NHEFJLLP_03362 | 2.3e-56 | dsbJ | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
NHEFJLLP_03363 | 8.4e-145 | yjfP | S | Dienelactone hydrolase family | ||
NHEFJLLP_03364 | 1.2e-67 | |||||
NHEFJLLP_03365 | 6.2e-96 | V | VanZ like family | |||
NHEFJLLP_03366 | 4.9e-63 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_03367 | 5.3e-99 | L | Integrase | |||
NHEFJLLP_03368 | 2.4e-22 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
NHEFJLLP_03369 | 7.6e-52 | L | Belongs to the 'phage' integrase family | |||
NHEFJLLP_03370 | 4e-95 | V | VanZ like family | |||
NHEFJLLP_03373 | 8.4e-66 | rusA | 3.1.22.4 | L | Endonuclease that resolves Holliday junction intermediates made during homologous genetic recombination and DNA repair. Exhibits sequence and structure-selective cleavage of four-way DNA junctions, where it introduces symmetrical nicks in two strands of the same polarity at the 5' side of dinucleotides. Corrects the defects in genetic recombination and DNA repair associated with inactivation of ruvAB or ruvC | |
NHEFJLLP_03374 | 3.4e-62 | |||||
NHEFJLLP_03376 | 4.9e-151 | S | IstB-like ATP binding protein | |||
NHEFJLLP_03377 | 6.2e-37 | L | Domain of unknown function (DUF4373) | |||
NHEFJLLP_03378 | 3.2e-61 | |||||
NHEFJLLP_03379 | 5.4e-55 | S | Bacteriophage Mu Gam like protein | |||
NHEFJLLP_03381 | 6.8e-12 | S | Domain of unknown function (DUF1508) | |||
NHEFJLLP_03382 | 2.4e-25 | |||||
NHEFJLLP_03384 | 4.6e-75 | |||||
NHEFJLLP_03385 | 2.2e-48 | |||||
NHEFJLLP_03389 | 3.9e-31 | S | Uncharacterized protein conserved in bacteria (DUF2188) | |||
NHEFJLLP_03392 | 6.3e-16 | K | sequence-specific DNA binding | |||
NHEFJLLP_03393 | 3.6e-09 | E | peptidase | |||
NHEFJLLP_03395 | 8.5e-11 | S | DNA/RNA non-specific endonuclease | |||
NHEFJLLP_03399 | 7.8e-24 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
NHEFJLLP_03400 | 3.2e-83 | yhcA | V | ABC transporter, ATP-binding protein | ||
NHEFJLLP_03401 | 1.5e-86 | cps4G | M | Glycosyltransferase Family 4 | ||
NHEFJLLP_03402 | 2.3e-79 | cps4G | M | Glycosyltransferase Family 4 | ||
NHEFJLLP_03403 | 8.9e-49 | clpB | O | C-terminal, D2-small domain, of ClpB protein | ||
NHEFJLLP_03404 | 1.8e-87 | manN | G | system, mannose fructose sorbose family IID component | ||
NHEFJLLP_03405 | 1.1e-72 | manN | G | system, mannose fructose sorbose family IID component | ||
NHEFJLLP_03406 | 1.6e-152 | K | LysR family | |||
NHEFJLLP_03407 | 0.0 | 1.3.5.4 | C | FMN_bind | ||
NHEFJLLP_03408 | 8e-255 | P | Sodium:sulfate symporter transmembrane region | |||
NHEFJLLP_03409 | 8.5e-43 | tnp2PF3 | L | Transposase | ||
NHEFJLLP_03410 | 8.5e-43 | S | protein conserved in bacteria | |||
NHEFJLLP_03411 | 2.1e-37 | |||||
NHEFJLLP_03412 | 2.6e-24 | |||||
NHEFJLLP_03413 | 0.0 | traA | L | MobA MobL family protein | ||
NHEFJLLP_03414 | 1.6e-110 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NHEFJLLP_03415 | 3.3e-130 | epsB | M | biosynthesis protein | ||
NHEFJLLP_03416 | 4.6e-129 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
NHEFJLLP_03417 | 7.3e-133 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NHEFJLLP_03418 | 3.1e-158 | S | Protein of unknown function (DUF2785) | |||
NHEFJLLP_03419 | 3.3e-25 | speG | J | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_03420 | 5.3e-48 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
NHEFJLLP_03421 | 5.2e-90 | ywkB | S | Membrane transport protein | ||
NHEFJLLP_03422 | 3e-56 | tarL | 2.7.8.14, 2.7.8.47 | H | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
NHEFJLLP_03423 | 1.5e-49 | |||||
NHEFJLLP_03424 | 4e-75 | S | Putative metallopeptidase domain | |||
NHEFJLLP_03425 | 9.4e-71 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NHEFJLLP_03426 | 4.2e-71 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NHEFJLLP_03427 | 4e-170 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
NHEFJLLP_03428 | 7.4e-175 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
NHEFJLLP_03429 | 7.6e-205 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
NHEFJLLP_03430 | 2.1e-196 | 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) | |
NHEFJLLP_03431 | 6e-196 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
NHEFJLLP_03432 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
NHEFJLLP_03433 | 1.6e-249 | malT | G | Major Facilitator | ||
NHEFJLLP_03435 | 3.8e-63 | S | Domain of unknown function (DUF4767) | |||
NHEFJLLP_03436 | 1.7e-102 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NHEFJLLP_03437 | 4e-55 | KT | response to antibiotic | |||
NHEFJLLP_03438 | 4.5e-22 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NHEFJLLP_03439 | 1.4e-46 | K | Helix-turn-helix domain | |||
NHEFJLLP_03440 | 1.6e-35 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
NHEFJLLP_03441 | 4.1e-135 | potD | P | ABC transporter | ||
NHEFJLLP_03442 | 1.4e-72 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_03443 | 7.4e-74 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
NHEFJLLP_03446 | 3.2e-164 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
NHEFJLLP_03447 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
NHEFJLLP_03448 | 1.7e-134 | stp | 3.1.3.16 | T | phosphatase | |
NHEFJLLP_03449 | 3e-251 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
NHEFJLLP_03450 | 1.2e-174 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
NHEFJLLP_03451 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
NHEFJLLP_03452 | 4.3e-218 | 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 | |
NHEFJLLP_03453 | 2.4e-30 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
NHEFJLLP_03454 | 3.3e-112 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
NHEFJLLP_03455 | 4.5e-55 | |||||
NHEFJLLP_03456 | 7.3e-61 | 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 | |
NHEFJLLP_03457 | 9.8e-34 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
NHEFJLLP_03458 | 1.4e-65 | 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 | ||
NHEFJLLP_03459 | 6.4e-66 | 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 | ||
NHEFJLLP_03460 | 3.1e-72 | |||||
NHEFJLLP_03461 | 5.6e-39 | S | Cytochrome B5 | |||
NHEFJLLP_03462 | 7.5e-89 | pts21A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
NHEFJLLP_03463 | 6.2e-218 | 2.7.7.65 | T | Diguanylate cyclase, GGDEF domain | ||
NHEFJLLP_03464 | 2.1e-75 | yliE | T | EAL domain | ||
NHEFJLLP_03465 | 6e-42 | yliE | T | EAL domain | ||
NHEFJLLP_03466 | 2.2e-104 | 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 | |
NHEFJLLP_03467 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
NHEFJLLP_03468 | 2e-80 | |||||
NHEFJLLP_03469 | 4.5e-73 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
NHEFJLLP_03470 | 6.8e-192 | 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 | |
NHEFJLLP_03471 | 1.5e-191 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
NHEFJLLP_03472 | 4.9e-22 | |||||
NHEFJLLP_03473 | 1e-13 | |||||
NHEFJLLP_03474 | 1.2e-67 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
NHEFJLLP_03475 | 4.7e-67 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
NHEFJLLP_03476 | 2.4e-40 | helD | 3.6.4.12 | L | DNA helicase | |
NHEFJLLP_03477 | 1e-37 | higA | K | Helix-turn-helix XRE-family like proteins | ||
NHEFJLLP_03478 | 1.4e-114 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
NHEFJLLP_03479 | 8.2e-18 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_03480 | 5.2e-123 | K | DeoR C terminal sensor domain | |||
NHEFJLLP_03481 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
NHEFJLLP_03482 | 1.5e-42 | yueI | S | Protein of unknown function (DUF1694) | ||
NHEFJLLP_03483 | 9.6e-103 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
NHEFJLLP_03484 | 7.8e-266 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
NHEFJLLP_03485 | 1e-136 | araD | 4.1.2.17, 4.1.2.19, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
NHEFJLLP_03486 | 6e-307 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.5 | G | carbohydrate kinase FGGY | |
NHEFJLLP_03487 | 6.7e-90 | araP | U | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
NHEFJLLP_03488 | 8.9e-148 | araP | U | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
NHEFJLLP_03489 | 1.4e-206 | araR | K | Transcriptional regulator | ||
NHEFJLLP_03490 | 3.4e-47 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | ||
NHEFJLLP_03491 | 1.9e-53 | L | Transposase | |||
NHEFJLLP_03492 | 2.9e-63 | |||||
NHEFJLLP_03493 | 3.1e-42 | estA | S | Putative esterase | ||
NHEFJLLP_03496 | 2.1e-38 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NHEFJLLP_03497 | 1.1e-203 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NHEFJLLP_03498 | 2.6e-27 | wcoI | 2.7.10.1, 2.7.10.2 | M | biosynthesis protein | |
NHEFJLLP_03499 | 4.3e-21 | D | protein tyrosine kinase activity | |||
NHEFJLLP_03500 | 8.8e-23 | V | Beta-lactamase | |||
NHEFJLLP_03501 | 1.7e-86 | cps1D | M | Domain of unknown function (DUF4422) | ||
NHEFJLLP_03502 | 1.4e-79 | cps3A | S | Glycosyltransferase like family 2 | ||
NHEFJLLP_03503 | 1.2e-45 | cps | M | Glycosyl transferase, family 2 | ||
NHEFJLLP_03504 | 7.3e-77 | sacB | GT2,GT4 | M | Stealth protein CR2, conserved region 2 | |
NHEFJLLP_03505 | 2.9e-87 | wzy | P | EpsG family | ||
NHEFJLLP_03506 | 1.3e-77 | 1.1.1.133 | S | Glycosyltransferase like family 2 | ||
NHEFJLLP_03507 | 2.3e-177 | rfbX | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
NHEFJLLP_03509 | 1.5e-74 | yeaL | S | Protein of unknown function (DUF441) | ||
NHEFJLLP_03510 | 3.3e-31 | estA | S | Putative esterase | ||
NHEFJLLP_03511 | 3.5e-61 | |||||
NHEFJLLP_03516 | 3.3e-115 | |||||
NHEFJLLP_03517 | 1.3e-116 | |||||
NHEFJLLP_03518 | 1.4e-53 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
NHEFJLLP_03519 | 6.4e-105 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
NHEFJLLP_03520 | 1.4e-49 | |||||
NHEFJLLP_03521 | 3.2e-229 | cps4J | S | Polysaccharide biosynthesis protein | ||
NHEFJLLP_03522 | 1.2e-194 | 2.1.1.21, 6.3.5.4 | E | Asparagine synthase | ||
NHEFJLLP_03523 | 4.1e-74 | tagD | 2.7.7.15, 2.7.7.39 | IM | Cytidylyltransferase-like | |
NHEFJLLP_03524 | 2e-233 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
NHEFJLLP_03525 | 8.2e-139 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
NHEFJLLP_03526 | 9.4e-190 | S | EpsG family | |||
NHEFJLLP_03527 | 7.2e-152 | epsE | GT2 | M | Glycosyltransferase like family 2 | |
NHEFJLLP_03528 | 1.3e-207 | M | Glycosyl transferases group 1 | |||
NHEFJLLP_03529 | 1.4e-119 | rfbP | M | Bacterial sugar transferase | ||
NHEFJLLP_03530 | 1.9e-26 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NHEFJLLP_03531 | 1.1e-30 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NHEFJLLP_03532 | 2e-124 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
NHEFJLLP_03533 | 3.7e-129 | epsB | M | biosynthesis protein | ||
NHEFJLLP_03534 | 9e-104 | K | transcriptional regulator | |||
NHEFJLLP_03536 | 8.9e-30 | |||||
NHEFJLLP_03537 | 1.7e-105 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
NHEFJLLP_03540 | 1.6e-123 | pepL | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
NHEFJLLP_03541 | 3e-173 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
NHEFJLLP_03542 | 2.3e-36 | tetR | K | Transcriptional regulator C-terminal region | ||
NHEFJLLP_03543 | 2.7e-68 | XK27_06930 | S | ABC-2 family transporter protein | ||
NHEFJLLP_03544 | 1.3e-28 | S | Putative metallopeptidase domain | |||
NHEFJLLP_03545 | 5.2e-59 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
NHEFJLLP_03546 | 1.2e-69 | S | LuxR family transcriptional regulator | |||
NHEFJLLP_03547 | 2e-58 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
NHEFJLLP_03548 | 3.5e-69 | S | LuxR family transcriptional regulator | |||
NHEFJLLP_03549 | 5.8e-21 | cycA | E | Amino acid permease | ||
NHEFJLLP_03550 | 2.1e-109 | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | ||
NHEFJLLP_03551 | 3.4e-32 | |||||
NHEFJLLP_03552 | 9.3e-198 | L | Psort location Cytoplasmic, score | |||
NHEFJLLP_03553 | 1.6e-25 | S | Domain of unknown function (DUF296) | |||
NHEFJLLP_03554 | 6.3e-47 | ydeP | K | Transcriptional regulators | ||
NHEFJLLP_03555 | 1.7e-67 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
NHEFJLLP_03556 | 2.9e-18 | K | transcriptional regulator | |||
NHEFJLLP_03557 | 1.5e-211 | lmrB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_03558 | 4.9e-46 | S | Domain of unknown function (DUF4811) | |||
NHEFJLLP_03559 | 1.1e-122 | Q | Psort location Cytoplasmic, score 8.87 | |||
NHEFJLLP_03560 | 5.6e-69 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_03561 | 1.1e-52 | S | Pfam:DUF3816 | |||
NHEFJLLP_03562 | 1.9e-216 | yifK | E | Amino acid permease | ||
NHEFJLLP_03563 | 2.6e-62 | |||||
NHEFJLLP_03564 | 1.7e-51 | |||||
NHEFJLLP_03565 | 6.1e-238 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
NHEFJLLP_03566 | 8.1e-68 | ydeA | S | intracellular protease amidase | ||
NHEFJLLP_03567 | 2.6e-38 | 3.5.1.124 | S | DJ-1/PfpI family | ||
NHEFJLLP_03568 | 2.3e-76 | S | Protein of unknown function with HXXEE motif | |||
NHEFJLLP_03569 | 1.6e-12 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_03570 | 1.3e-69 | L | Helix-turn-helix domain | |||
NHEFJLLP_03571 | 4.3e-245 | cycA | E | Amino acid permease | ||
NHEFJLLP_03572 | 2e-08 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
NHEFJLLP_03573 | 2e-65 | K | Transcriptional regulator PadR-like family | |||
NHEFJLLP_03574 | 1.3e-210 | K | Sigma-54 interaction domain | |||
NHEFJLLP_03575 | 1e-24 | 2.7.1.191 | G | PTS system fructose IIA component | ||
NHEFJLLP_03576 | 3.1e-57 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
NHEFJLLP_03577 | 1.5e-104 | G | PTS system sorbose-specific iic component | |||
NHEFJLLP_03578 | 2.6e-112 | G | PTS system mannose/fructose/sorbose family IID component | |||
NHEFJLLP_03579 | 2.6e-228 | malL | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein |
NHEFJLLP_03580 | 1.5e-32 | L | Transposase and inactivated derivatives, IS30 family | |||
NHEFJLLP_03581 | 1.5e-155 | aatB | ET | ABC transporter substrate-binding protein | ||
NHEFJLLP_03582 | 2.5e-115 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NHEFJLLP_03583 | 4.6e-109 | glnP | P | ABC transporter permease | ||
NHEFJLLP_03584 | 1.2e-146 | minD | D | Belongs to the ParA family | ||
NHEFJLLP_03585 | 1.1e-116 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
NHEFJLLP_03586 | 1.2e-88 | mreD | M | rod shape-determining protein MreD | ||
NHEFJLLP_03587 | 2.6e-144 | mreC | M | Involved in formation and maintenance of cell shape | ||
NHEFJLLP_03588 | 3.7e-161 | mreB | D | cell shape determining protein MreB | ||
NHEFJLLP_03589 | 1.3e-116 | radC | L | DNA repair protein | ||
NHEFJLLP_03590 | 1.3e-251 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
NHEFJLLP_03591 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
NHEFJLLP_03592 | 4.5e-126 | |||||
NHEFJLLP_03593 | 8.3e-128 | |||||
NHEFJLLP_03594 | 4.7e-31 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NHEFJLLP_03595 | 2.4e-30 | M | LysM domain | |||
NHEFJLLP_03596 | 2.4e-30 | M | LysM domain | |||
NHEFJLLP_03597 | 4.7e-31 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
NHEFJLLP_03599 | 1.7e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
NHEFJLLP_03600 | 1.9e-211 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
NHEFJLLP_03601 | 2.9e-131 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
NHEFJLLP_03602 | 3.6e-41 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
NHEFJLLP_03603 | 2e-126 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
NHEFJLLP_03604 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
NHEFJLLP_03605 | 1.1e-280 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
NHEFJLLP_03606 | 1.6e-188 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
NHEFJLLP_03607 | 9.9e-103 | 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 | |
NHEFJLLP_03608 | 2.3e-287 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
NHEFJLLP_03609 | 2.4e-215 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
NHEFJLLP_03610 | 8.3e-11 | XK27_07075 | S | CAAX protease self-immunity | ||
NHEFJLLP_03611 | 9.2e-10 | |||||
NHEFJLLP_03613 | 1e-75 | patA | 2.6.1.1 | E | Aminotransferase | |
NHEFJLLP_03614 | 6.8e-67 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_03615 | 2.3e-70 | EGP | Major facilitator Superfamily | |||
NHEFJLLP_03616 | 1.2e-74 | papX3 | K | Transcriptional regulator | ||
NHEFJLLP_03617 | 1.1e-75 | papX3 | K | Transcriptional regulator | ||
NHEFJLLP_03618 | 2.2e-63 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NHEFJLLP_03619 | 2.9e-165 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
NHEFJLLP_03620 | 2.4e-182 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NHEFJLLP_03621 | 4.5e-156 | ddpX | 3.4.13.22 | S | L,D-transpeptidase catalytic domain | |
NHEFJLLP_03622 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
NHEFJLLP_03623 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
NHEFJLLP_03624 | 2.6e-183 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
NHEFJLLP_03625 | 5.4e-275 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
NHEFJLLP_03626 | 4.8e-76 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
NHEFJLLP_03627 | 1.1e-77 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
NHEFJLLP_03628 | 4.2e-70 | S | Pyrimidine dimer DNA glycosylase | |||
NHEFJLLP_03629 | 1.6e-89 | folT | 2.7.13.3 | T | ECF transporter, substrate-specific component | |
NHEFJLLP_03630 | 3e-10 | |||||
NHEFJLLP_03631 | 9e-13 | ytgB | S | Transglycosylase associated protein | ||
NHEFJLLP_03632 | 9.3e-291 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
NHEFJLLP_03633 | 4.9e-78 | yneH | 1.20.4.1 | K | ArsC family | |
NHEFJLLP_03634 | 5.7e-135 | K | LytTr DNA-binding domain | |||
NHEFJLLP_03635 | 8.7e-160 | 2.7.13.3 | T | GHKL domain | ||
NHEFJLLP_03636 | 1.8e-12 | |||||
NHEFJLLP_03637 | 2.4e-67 | agrB | KOT | May be involved in the proteolytic processing of a quorum sensing system signal molecule precursor | ||
NHEFJLLP_03638 | 0.0 | clpL | O | C-terminal, D2-small domain, of ClpB protein | ||
NHEFJLLP_03640 | 2.5e-26 | |||||
NHEFJLLP_03641 | 5.1e-27 | |||||
NHEFJLLP_03642 | 6.5e-81 | C | Zinc-binding dehydrogenase | |||
NHEFJLLP_03643 | 4.7e-66 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
NHEFJLLP_03644 | 3.2e-53 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
NHEFJLLP_03645 | 9.3e-106 | GBS0088 | S | Nucleotidyltransferase | ||
NHEFJLLP_03646 | 1.4e-106 | |||||
NHEFJLLP_03647 | 7.9e-117 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
NHEFJLLP_03648 | 3.3e-112 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_03649 | 1e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
NHEFJLLP_03650 | 0.0 | |||||
NHEFJLLP_03651 | 2.7e-61 | |||||
NHEFJLLP_03652 | 1.4e-192 | S | Fn3-like domain | |||
NHEFJLLP_03653 | 5.2e-103 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_03654 | 1.3e-77 | S | WxL domain surface cell wall-binding | |||
NHEFJLLP_03655 | 2.9e-73 | P | Sodium:sulfate symporter transmembrane region | |||
NHEFJLLP_03656 | 1e-60 | 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 | |
NHEFJLLP_03657 | 7.7e-82 | C | Zinc-binding dehydrogenase | |||
NHEFJLLP_03658 | 1.5e-36 | T | Belongs to the universal stress protein A family | |||
NHEFJLLP_03659 | 1e-63 | K | Winged helix DNA-binding domain | |||
NHEFJLLP_03660 | 8.2e-102 | L | Integrase | |||
NHEFJLLP_03661 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
NHEFJLLP_03662 | 6.5e-30 | |||||
NHEFJLLP_03663 | 2.7e-39 | ptsH | G | phosphocarrier protein HPR | ||
NHEFJLLP_03664 | 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) | |
NHEFJLLP_03665 | 1.4e-223 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
NHEFJLLP_03666 | 6.9e-200 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
NHEFJLLP_03667 | 7.4e-189 | mprF | I | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
NHEFJLLP_03668 | 5.6e-80 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
NHEFJLLP_03669 | 4.5e-55 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NHEFJLLP_03670 | 1.1e-53 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NHEFJLLP_03671 | 2e-200 | yhdP | S | Transporter associated domain | ||
NHEFJLLP_03672 | 4.9e-87 | nrdI | F | Belongs to the NrdI family | ||
NHEFJLLP_03673 | 2.2e-269 | yjcE | P | Sodium proton antiporter | ||
NHEFJLLP_03674 | 1.1e-212 | yttB | EGP | Major facilitator Superfamily | ||
NHEFJLLP_03675 | 1.2e-61 | K | helix_turn_helix, mercury resistance | |||
NHEFJLLP_03676 | 1.8e-173 | C | Zinc-binding dehydrogenase | |||
NHEFJLLP_03677 | 8.5e-57 | S | SdpI/YhfL protein family | |||
NHEFJLLP_03678 | 3.2e-294 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
NHEFJLLP_03679 | 5.5e-261 | gabR | K | Bacterial regulatory proteins, gntR family | ||
NHEFJLLP_03680 | 2.5e-76 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
NHEFJLLP_03682 | 7.9e-11 | M | domain protein | |||
NHEFJLLP_03683 | 2.3e-50 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
NHEFJLLP_03684 | 2.3e-50 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
NHEFJLLP_03685 | 5.4e-66 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
NHEFJLLP_03686 | 5.4e-66 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
NHEFJLLP_03687 | 2.3e-75 | T | Universal stress protein family | |||
NHEFJLLP_03688 | 1.2e-225 | pbuG | S | permease | ||
NHEFJLLP_03689 | 1.5e-19 | |||||
NHEFJLLP_03690 | 1.3e-82 | K | Transcriptional regulator | |||
NHEFJLLP_03691 | 5e-153 | licD | M | LicD family | ||
NHEFJLLP_03692 | 1.8e-289 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
NHEFJLLP_03693 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
NHEFJLLP_03694 | 3.2e-175 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
NHEFJLLP_03695 | 6.5e-78 | F | DNA/RNA non-specific endonuclease | |||
NHEFJLLP_03696 | 5.7e-97 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
NHEFJLLP_03697 | 3.9e-99 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
NHEFJLLP_03698 | 4.6e-91 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
NHEFJLLP_03699 | 1.1e-248 | dnaB | L | replication initiation and membrane attachment | ||
NHEFJLLP_03700 | 3.3e-172 | dnaI | L | Primosomal protein DnaI | ||
NHEFJLLP_03701 | 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) | |
NHEFJLLP_03702 | 1.8e-84 | 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 | ||
NHEFJLLP_03703 | 1.9e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
NHEFJLLP_03704 | 7.3e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
NHEFJLLP_03705 | 1.1e-55 | |||||
NHEFJLLP_03706 | 5e-240 | yrvN | L | AAA C-terminal domain | ||
NHEFJLLP_03707 | 6.1e-196 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
NHEFJLLP_03708 | 3.1e-37 | |||||
NHEFJLLP_03709 | 1.3e-28 | S | Psort location Cytoplasmic, score | |||
NHEFJLLP_03710 | 8.3e-57 | T | diguanylate cyclase | |||
NHEFJLLP_03711 | 1.7e-20 | ybbJ | K | Acetyltransferase (GNAT) family | ||
NHEFJLLP_03712 | 1.3e-54 | T | diguanylate cyclase | |||
NHEFJLLP_03713 | 1.1e-24 | S | Psort location Cytoplasmic, score | |||
NHEFJLLP_03714 | 6e-73 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
NHEFJLLP_03715 | 9.8e-79 | S | Uncharacterized protein conserved in bacteria (DUF2255) | |||
NHEFJLLP_03716 | 1.2e-160 | K | Transcriptional regulator | |||
NHEFJLLP_03717 | 8.7e-173 | C | nadph quinone reductase | |||
NHEFJLLP_03718 | 2.8e-14 | S | Alpha beta hydrolase | |||
NHEFJLLP_03719 | 1.1e-269 | nox | C | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
NHEFJLLP_03720 | 1.2e-103 | desR | K | helix_turn_helix, Lux Regulon | ||
NHEFJLLP_03721 | 2.2e-204 | desK | 2.7.13.3 | T | Histidine kinase | |
NHEFJLLP_03722 | 1.3e-134 | yvfS | V | ABC-2 type transporter | ||
NHEFJLLP_03723 | 5.2e-159 | yvfR | V | ABC transporter | ||
NHEFJLLP_03725 | 2.3e-81 | K | Acetyltransferase (GNAT) domain | |||
NHEFJLLP_03726 | 4.8e-73 | K | MarR family | |||
NHEFJLLP_03727 | 1e-114 | S | Psort location CytoplasmicMembrane, score | |||
NHEFJLLP_03728 | 1.1e-56 | |||||
NHEFJLLP_03729 | 4.7e-208 | 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 | ||
NHEFJLLP_03730 | 3.3e-52 | trxA | O | Belongs to the thioredoxin family | ||
NHEFJLLP_03731 | 7.6e-126 | yslB | S | Protein of unknown function (DUF2507) | ||
NHEFJLLP_03732 | 4.1e-150 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
NHEFJLLP_03733 | 1e-110 | 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 | |
NHEFJLLP_03734 | 9.5e-97 | S | Phosphoesterase | |||
NHEFJLLP_03735 | 6.5e-87 | ykuL | S | (CBS) domain | ||
NHEFJLLP_03736 | 2.6e-76 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
NHEFJLLP_03737 | 3.7e-226 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
NHEFJLLP_03738 | 2.6e-158 | ykuT | M | mechanosensitive ion channel | ||
NHEFJLLP_03739 | 1.9e-23 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
NHEFJLLP_03740 | 2.8e-56 | |||||
NHEFJLLP_03741 | 1.1e-80 | K | helix_turn_helix, mercury resistance | |||
NHEFJLLP_03742 | 1.7e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
NHEFJLLP_03743 | 1.9e-181 | ccpA | K | catabolite control protein A | ||
NHEFJLLP_03744 | 5.8e-163 | 3.2.1.52 | GH20 | G | Xylose isomerase domain protein TIM barrel | |
NHEFJLLP_03745 | 5.4e-50 | S | DsrE/DsrF-like family | |||
NHEFJLLP_03746 | 8.3e-131 | yebC | K | Transcriptional regulatory protein | ||
NHEFJLLP_03747 | 4.8e-160 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
NHEFJLLP_03748 | 5.6e-175 | comGA | NU | Type II IV secretion system protein | ||
NHEFJLLP_03749 | 9.6e-189 | comGB | NU | type II secretion system | ||
NHEFJLLP_03750 | 5.5e-43 | comGC | U | competence protein ComGC | ||
NHEFJLLP_03751 | 3.2e-83 | gspG | NU | general secretion pathway protein | ||
NHEFJLLP_03752 | 8.6e-20 | |||||
NHEFJLLP_03753 | 4.5e-88 | S | Prokaryotic N-terminal methylation motif | |||
NHEFJLLP_03755 | 1.2e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
NHEFJLLP_03756 | 7e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NHEFJLLP_03757 | 2.1e-252 | cycA | E | Amino acid permease | ||
NHEFJLLP_03758 | 4.4e-117 | S | Calcineurin-like phosphoesterase | |||
NHEFJLLP_03759 | 1.3e-270 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
NHEFJLLP_03760 | 1.5e-80 | yutD | S | Protein of unknown function (DUF1027) | ||
NHEFJLLP_03761 | 1.5e-146 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
NHEFJLLP_03762 | 4.6e-117 | S | Protein of unknown function (DUF1461) | |||
NHEFJLLP_03763 | 8.6e-119 | dedA | S | SNARE-like domain protein | ||
NHEFJLLP_03764 | 5.5e-109 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
NHEFJLLP_03765 | 1.6e-75 | yugI | 5.3.1.9 | J | general stress protein | |
NHEFJLLP_03766 | 3.5e-64 | |||||
NHEFJLLP_03767 | 2.4e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
NHEFJLLP_03768 | 7.4e-64 | yodB | K | Transcriptional regulator, HxlR family | ||
NHEFJLLP_03769 | 1.3e-93 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
NHEFJLLP_03770 | 7.9e-140 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NHEFJLLP_03771 | 6.4e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
NHEFJLLP_03772 | 1e-162 | 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 | ||
NHEFJLLP_03773 | 8.4e-94 | S | SdpI/YhfL protein family | |||
NHEFJLLP_03774 | 1.3e-226 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
NHEFJLLP_03775 | 4.1e-68 | S | Protein of unknown function (DUF1722) | |||
NHEFJLLP_03776 | 2.8e-38 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
NHEFJLLP_03777 | 4.6e-50 | 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 | ||
NHEFJLLP_03778 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
NHEFJLLP_03779 | 1.1e-47 | ylxQ | J | ribosomal protein | ||
NHEFJLLP_03780 | 9.5e-49 | ylxR | K | Protein of unknown function (DUF448) | ||
NHEFJLLP_03781 | 3.3e-217 | nusA | K | Participates in both transcription termination and antitermination | ||
NHEFJLLP_03782 | 4.2e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
NHEFJLLP_03783 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NHEFJLLP_03784 | 1.1e-71 | entB | 3.5.1.19 | Q | Isochorismatase family | |
NHEFJLLP_03785 | 4.7e-42 | |||||
NHEFJLLP_03786 | 1.9e-74 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
NHEFJLLP_03787 | 5.5e-43 | |||||
NHEFJLLP_03788 | 7.8e-97 | coiA | 3.6.4.12 | S | Competence protein | |
NHEFJLLP_03789 | 2e-97 | coiA | 3.6.4.12 | S | Competence protein | |
NHEFJLLP_03790 | 1.1e-161 | rrmA | 2.1.1.187 | H | Methyltransferase | |
NHEFJLLP_03791 | 1.7e-41 | 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 | ||
NHEFJLLP_03792 | 4.3e-206 | XK27_05220 | S | AI-2E family transporter | ||
NHEFJLLP_03793 | 3.9e-57 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
NHEFJLLP_03794 | 7.4e-194 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
NHEFJLLP_03795 | 5.1e-116 | cutC | P | Participates in the control of copper homeostasis | ||
NHEFJLLP_03796 | 4.4e-174 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
NHEFJLLP_03797 | 4.7e-151 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
NHEFJLLP_03798 | 2.7e-120 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
NHEFJLLP_03799 | 3.6e-114 | yjbH | Q | Thioredoxin | ||
NHEFJLLP_03800 | 0.0 | pepF | E | oligoendopeptidase F | ||
NHEFJLLP_03801 | 8.7e-93 | |||||
NHEFJLLP_03802 | 2.3e-90 | |||||
NHEFJLLP_03804 | 7.9e-48 | yhgE | V | domain protein | ||
NHEFJLLP_03805 | 7.9e-48 | yhgE | V | domain protein | ||
NHEFJLLP_03806 | 1e-47 | K | sequence-specific DNA binding | |||
NHEFJLLP_03807 | 7.8e-48 | K | sequence-specific DNA binding | |||
NHEFJLLP_03808 | 2.4e-42 | S | Cysteine-rich secretory protein family | |||
NHEFJLLP_03809 | 1.8e-168 | P | Natural resistance-associated macrophage protein | |||
NHEFJLLP_03810 | 3.1e-105 | L | Resolvase, N terminal domain | |||
NHEFJLLP_03811 | 6.2e-160 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
NHEFJLLP_03812 | 8.7e-102 | |||||
NHEFJLLP_03813 | 4e-122 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NHEFJLLP_03814 | 1.5e-78 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
NHEFJLLP_03816 | 2.7e-34 | 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 | ||
NHEFJLLP_03817 | 2.3e-11 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NHEFJLLP_03819 | 4e-10 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
NHEFJLLP_03820 | 4.6e-25 | S | Cysteine-rich secretory protein family | |||
NHEFJLLP_03821 | 6.1e-51 | yjhB | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | |
NHEFJLLP_03824 | 3.4e-32 | L | transposase activity | |||
NHEFJLLP_03826 | 2.4e-104 | K | Bacterial regulatory proteins, tetR family | |||
NHEFJLLP_03827 | 9.2e-65 | S | Domain of unknown function (DUF4440) | |||
NHEFJLLP_03828 | 1.4e-257 | qacA | EGP | Fungal trichothecene efflux pump (TRI12) | ||
NHEFJLLP_03829 | 3.2e-77 | 3.5.4.1 | GM | SnoaL-like domain | ||
NHEFJLLP_03830 | 3.7e-108 | GM | NAD(P)H-binding | |||
NHEFJLLP_03831 | 4.6e-112 | akr5f | 1.1.1.346 | S | reductase | |
NHEFJLLP_03832 | 2.1e-104 | M | ErfK YbiS YcfS YnhG | |||
NHEFJLLP_03833 | 4.3e-99 | acmD | 3.2.1.17 | NU | Bacterial SH3 domain | |
NHEFJLLP_03834 | 2.6e-94 | |||||
NHEFJLLP_03835 | 2.5e-92 | |||||
NHEFJLLP_03836 | 2.5e-98 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
NHEFJLLP_03837 | 2.5e-98 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
NHEFJLLP_03838 | 7.3e-55 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
NHEFJLLP_03839 | 2.4e-35 | yphH | S | Cupin domain | ||
NHEFJLLP_03840 | 2.5e-55 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
NHEFJLLP_03841 | 2.4e-35 | yphH | S | Cupin domain | ||
NHEFJLLP_03843 | 1e-15 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
NHEFJLLP_03844 | 5.1e-223 | malY | 4.4.1.8 | E | Aminotransferase class I and II | |
NHEFJLLP_03845 | 1.2e-269 | frvB | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NHEFJLLP_03846 | 3.3e-74 | ptsN | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
NHEFJLLP_03847 | 3.7e-79 | ptsG | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |
NHEFJLLP_03848 | 6.7e-148 | yleF | K | Helix-turn-helix domain, rpiR family | ||
NHEFJLLP_03849 | 1.6e-245 | sacX | 2.7.1.193, 2.7.1.211 | G | phosphotransferase system | |
NHEFJLLP_03850 | 5.4e-156 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
NHEFJLLP_03851 | 4.6e-199 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
NHEFJLLP_03853 | 4.4e-19 | f42a | O | Band 7 protein | ||
NHEFJLLP_03854 | 4.8e-55 | N | Cell shape-determining protein MreB | |||
NHEFJLLP_03855 | 1.9e-17 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
NHEFJLLP_03856 | 3.2e-74 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
NHEFJLLP_03857 | 8e-125 | crtI | 1.3.99.26, 1.3.99.28, 1.3.99.29, 1.3.99.31 | Q | Flavin containing amine oxidoreductase | |
NHEFJLLP_03858 | 8.2e-165 | crtB | 2.5.1.21, 2.5.1.32, 2.5.1.99 | I | Squalene/phytoene synthase | |
NHEFJLLP_03859 | 1.1e-183 | D | Alpha beta | |||
NHEFJLLP_03860 | 6.4e-199 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NHEFJLLP_03861 | 8.1e-257 | gor | 1.8.1.7 | C | Glutathione reductase | |
NHEFJLLP_03862 | 3.4e-55 | S | Enterocin A Immunity | |||
NHEFJLLP_03863 | 7.4e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
NHEFJLLP_03864 | 4e-253 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
NHEFJLLP_03865 | 1.3e-184 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
NHEFJLLP_03866 | 1.3e-28 | |||||
NHEFJLLP_03867 | 2.4e-53 | azoB | GM | NmrA-like family | ||
NHEFJLLP_03868 | 1.1e-53 | azoB | GM | NmrA-like family | ||
NHEFJLLP_03869 | 1.5e-244 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
NHEFJLLP_03870 | 1.1e-172 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
NHEFJLLP_03871 | 3.2e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NHEFJLLP_03872 | 1e-298 | pucR | QT | Purine catabolism regulatory protein-like family | ||
NHEFJLLP_03873 | 2.7e-236 | pbuX | F | xanthine permease | ||
NHEFJLLP_03874 | 2.4e-221 | pbuG | S | Permease family | ||
NHEFJLLP_03875 | 3.9e-162 | GM | NmrA-like family | |||
NHEFJLLP_03876 | 9.8e-52 | |||||
NHEFJLLP_03877 | 7.8e-15 | |||||
NHEFJLLP_03878 | 7.2e-14 | |||||
NHEFJLLP_03880 | 2.2e-12 | arpU | S | Phage transcriptional regulator, ArpU family | ||
NHEFJLLP_03887 | 1.9e-41 | L | HNH endonuclease | |||
NHEFJLLP_03888 | 3.2e-28 | L | Phage terminase, small subunit | |||
NHEFJLLP_03889 | 2.6e-216 | S | Phage Terminase | |||
NHEFJLLP_03891 | 2.3e-135 | S | Phage portal protein | |||
NHEFJLLP_03892 | 3.8e-72 | yhbO | 3.5.1.124 | S | DJ-1/PfpI family | |
NHEFJLLP_03893 | 1.6e-54 | L | Transposase | |||
NHEFJLLP_03894 | 1.2e-216 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
NHEFJLLP_03895 | 4.4e-59 | qacC | P | Small Multidrug Resistance protein | ||
NHEFJLLP_03896 | 7.3e-44 | qacH | U | Small Multidrug Resistance protein | ||
NHEFJLLP_03897 | 3e-116 | hly | S | protein, hemolysin III | ||
NHEFJLLP_03898 | 5.1e-54 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
NHEFJLLP_03899 | 2.7e-160 | czcD | P | cation diffusion facilitator family transporter | ||
NHEFJLLP_03900 | 7.8e-103 | K | Helix-turn-helix XRE-family like proteins | |||
NHEFJLLP_03902 | 2.6e-19 | |||||
NHEFJLLP_03903 | 6.5e-96 | tag | 3.2.2.20 | L | glycosylase | |
NHEFJLLP_03904 | 2.3e-212 | folP | 2.5.1.15 | H | dihydropteroate synthase | |
NHEFJLLP_03905 | 2.7e-35 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
NHEFJLLP_03906 | 7e-81 | manY | G | PTS system | ||
NHEFJLLP_03907 | 2.6e-68 | manY | G | PTS system | ||
NHEFJLLP_03908 | 4.3e-92 | |||||
NHEFJLLP_03909 | 2.2e-91 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)