ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HMPBNJCG_00005 | 5.5e-139 | mreC | M | Involved in formation and maintenance of cell shape | ||
HMPBNJCG_00006 | 6.3e-88 | mreD | M | Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins | ||
HMPBNJCG_00007 | 1.7e-90 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
HMPBNJCG_00008 | 1.2e-174 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
HMPBNJCG_00009 | 2.9e-218 | araT | 2.6.1.1 | E | Aminotransferase | |
HMPBNJCG_00010 | 2.6e-143 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HMPBNJCG_00011 | 1.3e-179 | 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 | |
HMPBNJCG_00012 | 4.2e-34 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HMPBNJCG_00013 | 2e-129 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HMPBNJCG_00014 | 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 | |
HMPBNJCG_00015 | 1.3e-276 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HMPBNJCG_00016 | 1.8e-184 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HMPBNJCG_00017 | 1.4e-101 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
HMPBNJCG_00018 | 2.3e-295 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HMPBNJCG_00019 | 6.1e-79 | L | transposase activity | |||
HMPBNJCG_00020 | 1.3e-49 | L | transposition | |||
HMPBNJCG_00021 | 6.3e-34 | L | Integrase core domain protein | |||
HMPBNJCG_00022 | 2.3e-161 | S | CHAP domain | |||
HMPBNJCG_00023 | 3.4e-241 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HMPBNJCG_00024 | 3.8e-70 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HMPBNJCG_00025 | 2.2e-204 | 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) | |
HMPBNJCG_00026 | 9.2e-141 | 1.1.1.169 | H | Ketopantoate reductase | ||
HMPBNJCG_00027 | 8.7e-248 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
HMPBNJCG_00028 | 0.0 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
HMPBNJCG_00029 | 1.2e-09 | L | Transposase | |||
HMPBNJCG_00030 | 7.8e-211 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
HMPBNJCG_00031 | 8.3e-221 | nodC | 2.4.1.212 | GT2 | M | Chitin synthase |
HMPBNJCG_00032 | 6.5e-54 | L | transposition | |||
HMPBNJCG_00033 | 7.7e-19 | L | transposase activity | |||
HMPBNJCG_00034 | 2.5e-40 | L | Transposase | |||
HMPBNJCG_00035 | 0.0 | 3.6.3.8 | P | cation transport ATPase | ||
HMPBNJCG_00036 | 0.0 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | component I | |
HMPBNJCG_00037 | 1.9e-105 | V | Abi-like protein | |||
HMPBNJCG_00039 | 2.3e-12 | |||||
HMPBNJCG_00041 | 2e-296 | S | DNA primase | |||
HMPBNJCG_00042 | 3e-164 | KL | Phage plasmid primase P4 family | |||
HMPBNJCG_00043 | 2.4e-22 | |||||
HMPBNJCG_00044 | 1.2e-14 | |||||
HMPBNJCG_00048 | 1.8e-19 | K | Cro/C1-type HTH DNA-binding domain | |||
HMPBNJCG_00049 | 1e-21 | xre | K | transcriptional | ||
HMPBNJCG_00050 | 6.9e-220 | sip | L | Belongs to the 'phage' integrase family | ||
HMPBNJCG_00052 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HMPBNJCG_00053 | 7.3e-166 | metF | 1.5.1.20 | E | reductase | |
HMPBNJCG_00054 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
HMPBNJCG_00055 | 1.7e-94 | panT | S | ECF transporter, substrate-specific component | ||
HMPBNJCG_00056 | 4.8e-94 | 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 | |
HMPBNJCG_00057 | 1.2e-120 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
HMPBNJCG_00058 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HMPBNJCG_00059 | 6.4e-66 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HMPBNJCG_00060 | 2.8e-40 | T | PhoQ Sensor | |||
HMPBNJCG_00061 | 1.7e-43 | T | PhoQ Sensor | |||
HMPBNJCG_00062 | 5.8e-79 | T | PhoQ Sensor | |||
HMPBNJCG_00063 | 2.1e-30 | rpsT | J | rRNA binding | ||
HMPBNJCG_00064 | 1.9e-172 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
HMPBNJCG_00065 | 1.8e-107 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
HMPBNJCG_00066 | 1.2e-57 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
HMPBNJCG_00067 | 6e-98 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
HMPBNJCG_00068 | 1.4e-22 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
HMPBNJCG_00069 | 4e-63 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
HMPBNJCG_00070 | 1.3e-69 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
HMPBNJCG_00071 | 9.5e-192 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
HMPBNJCG_00072 | 3.7e-282 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
HMPBNJCG_00073 | 4.7e-191 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
HMPBNJCG_00074 | 4.8e-171 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
HMPBNJCG_00075 | 8.9e-121 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
HMPBNJCG_00076 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
HMPBNJCG_00077 | 3.1e-81 | ypmB | S | Protein conserved in bacteria | ||
HMPBNJCG_00078 | 6.5e-218 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
HMPBNJCG_00079 | 1.7e-262 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
HMPBNJCG_00080 | 1.5e-07 | |||||
HMPBNJCG_00081 | 3e-13 | |||||
HMPBNJCG_00082 | 3e-63 | tdcF | 3.5.99.10 | J | endoribonuclease L-PSP | |
HMPBNJCG_00083 | 2e-123 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
HMPBNJCG_00084 | 2.2e-81 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
HMPBNJCG_00085 | 3.9e-133 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
HMPBNJCG_00086 | 2.5e-94 | queF | 1.7.1.13 | S | Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily | |
HMPBNJCG_00087 | 4.2e-18 | D | nuclear chromosome segregation | |||
HMPBNJCG_00088 | 1.5e-135 | yejC | S | cyclic nucleotide-binding protein | ||
HMPBNJCG_00089 | 1.2e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
HMPBNJCG_00090 | 1.8e-181 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HMPBNJCG_00091 | 8.7e-162 | whiA | K | May be required for sporulation | ||
HMPBNJCG_00092 | 8e-90 | pepD | E | Dipeptidase | ||
HMPBNJCG_00093 | 5.8e-41 | pepD | E | dipeptidase activity | ||
HMPBNJCG_00094 | 5.4e-32 | cspD | K | Cold shock protein domain | ||
HMPBNJCG_00095 | 9.4e-43 | K | Cold-Shock Protein | |||
HMPBNJCG_00096 | 3.3e-222 | L | Transposase | |||
HMPBNJCG_00097 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
HMPBNJCG_00098 | 2.3e-170 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HMPBNJCG_00099 | 2.7e-219 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
HMPBNJCG_00100 | 1.5e-95 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
HMPBNJCG_00101 | 4.8e-157 | glcU | U | Glucose uptake | ||
HMPBNJCG_00102 | 1.8e-08 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
HMPBNJCG_00103 | 5.9e-79 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
HMPBNJCG_00104 | 2.2e-101 | XK27_10720 | D | peptidase activity | ||
HMPBNJCG_00105 | 3.1e-292 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HMPBNJCG_00106 | 1.7e-08 | |||||
HMPBNJCG_00108 | 1.2e-172 | yeiH | S | Membrane | ||
HMPBNJCG_00109 | 5.5e-119 | mur1 | NU | muramidase | ||
HMPBNJCG_00110 | 1.9e-83 | L | transposition | |||
HMPBNJCG_00111 | 2.6e-166 | cpsY | K | Transcriptional regulator | ||
HMPBNJCG_00112 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
HMPBNJCG_00113 | 1.2e-57 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
HMPBNJCG_00114 | 2e-104 | artQ | P | ABC transporter (Permease | ||
HMPBNJCG_00115 | 1.8e-113 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HMPBNJCG_00116 | 1.1e-158 | aatB | ET | ABC transporter substrate-binding protein | ||
HMPBNJCG_00117 | 3.5e-40 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HMPBNJCG_00118 | 2.5e-139 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HMPBNJCG_00119 | 1.7e-57 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
HMPBNJCG_00120 | 1.3e-106 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
HMPBNJCG_00121 | 9.3e-20 | sthIM | 2.1.1.72 | L | Adenine specific DNA methylase Mod | |
HMPBNJCG_00122 | 3.9e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HMPBNJCG_00123 | 4.5e-126 | gntR1 | K | transcriptional | ||
HMPBNJCG_00124 | 1.1e-53 | 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 | ||
HMPBNJCG_00125 | 1.3e-269 | 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 | |
HMPBNJCG_00126 | 4.1e-87 | niaX | ||||
HMPBNJCG_00127 | 8.6e-90 | niaR | S | small molecule binding protein (contains 3H domain) | ||
HMPBNJCG_00128 | 6.9e-127 | K | DNA-binding helix-turn-helix protein | |||
HMPBNJCG_00129 | 1.4e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
HMPBNJCG_00130 | 1.5e-135 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HMPBNJCG_00131 | 4.1e-167 | GK | ROK family | |||
HMPBNJCG_00132 | 8.3e-159 | dprA | LU | DNA protecting protein DprA | ||
HMPBNJCG_00133 | 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 | |
HMPBNJCG_00134 | 1.4e-150 | S | TraX protein | |||
HMPBNJCG_00135 | 2.2e-122 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HMPBNJCG_00136 | 2.4e-251 | T | PhoQ Sensor | |||
HMPBNJCG_00137 | 6.6e-259 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
HMPBNJCG_00138 | 1.1e-152 | XK27_05470 | E | Methionine synthase | ||
HMPBNJCG_00139 | 1.7e-75 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
HMPBNJCG_00140 | 2.7e-48 | pspE | P | 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 | ||
HMPBNJCG_00141 | 1.8e-51 | IQ | Acetoin reductase | |||
HMPBNJCG_00142 | 3.9e-19 | IQ | Acetoin reductase | |||
HMPBNJCG_00143 | 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 | ||
HMPBNJCG_00144 | 1.8e-156 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
HMPBNJCG_00147 | 1.3e-212 | pqqE | C | radical SAM domain protein | ||
HMPBNJCG_00148 | 3.9e-136 | speB | 3.5.3.11 | E | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines | |
HMPBNJCG_00149 | 6.6e-61 | EGP | Major facilitator Superfamily | |||
HMPBNJCG_00150 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
HMPBNJCG_00151 | 3e-133 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
HMPBNJCG_00152 | 8.6e-196 | L | Transposase | |||
HMPBNJCG_00153 | 6.4e-104 | V | ABC transporter (Permease | |||
HMPBNJCG_00154 | 4.1e-114 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
HMPBNJCG_00155 | 1.6e-10 | |||||
HMPBNJCG_00156 | 1.2e-97 | K | Transcriptional regulator, TetR family | |||
HMPBNJCG_00157 | 1.2e-158 | czcD | P | cation diffusion facilitator family transporter | ||
HMPBNJCG_00158 | 2.7e-210 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
HMPBNJCG_00159 | 6.2e-196 | adhB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
HMPBNJCG_00160 | 6e-08 | S | Hydrolases of the alpha beta superfamily | |||
HMPBNJCG_00161 | 7.9e-17 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HMPBNJCG_00162 | 3.8e-78 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HMPBNJCG_00163 | 7.6e-134 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
HMPBNJCG_00164 | 4.1e-143 | |||||
HMPBNJCG_00165 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
HMPBNJCG_00166 | 7.6e-160 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
HMPBNJCG_00167 | 1.9e-109 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
HMPBNJCG_00168 | 6.8e-185 | pelG | M | Putative exopolysaccharide Exporter (EPS-E) | ||
HMPBNJCG_00169 | 1.5e-211 | cotH | M | CotH kinase protein | ||
HMPBNJCG_00170 | 8.4e-53 | G | Domain of unknown function (DUF4832) | |||
HMPBNJCG_00171 | 4.9e-21 | G | Domain of unknown function (DUF4832) | |||
HMPBNJCG_00172 | 3.7e-193 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HMPBNJCG_00174 | 7.2e-231 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HMPBNJCG_00175 | 1.2e-25 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
HMPBNJCG_00176 | 1.4e-124 | endA | F | DNA RNA non-specific endonuclease | ||
HMPBNJCG_00177 | 4.2e-110 | tcyB_2 | P | ABC transporter (permease) | ||
HMPBNJCG_00178 | 8e-115 | gltJ | P | ABC transporter (Permease | ||
HMPBNJCG_00179 | 3.5e-149 | peb1A | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
HMPBNJCG_00180 | 1e-139 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HMPBNJCG_00181 | 9.9e-129 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HMPBNJCG_00182 | 1.5e-247 | vicK | 2.7.13.3 | T | Histidine kinase | |
HMPBNJCG_00183 | 2.1e-154 | vicX | 3.1.26.11 | S | Metal-dependent hydrolases of the beta-lactamase superfamily I | |
HMPBNJCG_00184 | 9e-231 | murM | 2.3.2.10, 2.3.2.16 | V | protein involved in methicillin resistance | |
HMPBNJCG_00185 | 9.2e-147 | yidA | S | hydrolases of the HAD superfamily | ||
HMPBNJCG_00186 | 6.3e-51 | XK27_00115 | 2.3.1.128 | K | acetyltransferase | |
HMPBNJCG_00187 | 2.6e-67 | ywiB | S | Domain of unknown function (DUF1934) | ||
HMPBNJCG_00188 | 0.0 | pacL | 3.6.3.8 | P | cation transport ATPase | |
HMPBNJCG_00189 | 5.2e-136 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HMPBNJCG_00190 | 4.3e-180 | yjjH | S | Calcineurin-like phosphoesterase | ||
HMPBNJCG_00191 | 1.2e-202 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
HMPBNJCG_00192 | 1.8e-181 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HMPBNJCG_00193 | 2.5e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
HMPBNJCG_00194 | 3.6e-163 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
HMPBNJCG_00195 | 3.5e-93 | mutX | 3.6.1.55 | F | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
HMPBNJCG_00196 | 1.1e-175 | yubA | S | permease | ||
HMPBNJCG_00197 | 4.9e-224 | G | COG0457 FOG TPR repeat | |||
HMPBNJCG_00198 | 4.2e-98 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HMPBNJCG_00199 | 1.8e-234 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
HMPBNJCG_00200 | 2.9e-90 | ebsA | S | Family of unknown function (DUF5322) | ||
HMPBNJCG_00201 | 3.9e-15 | M | LysM domain | |||
HMPBNJCG_00202 | 2.8e-120 | 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 | |
HMPBNJCG_00203 | 3.5e-86 | 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 | ||
HMPBNJCG_00204 | 2.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HMPBNJCG_00205 | 1.5e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
HMPBNJCG_00206 | 9.1e-10 | L | COG1943 Transposase and inactivated derivatives | |||
HMPBNJCG_00207 | 6.9e-86 | XK27_03610 | K | Gnat family | ||
HMPBNJCG_00208 | 3.2e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
HMPBNJCG_00209 | 2.4e-275 | pepV | 3.5.1.18 | E | Dipeptidase | |
HMPBNJCG_00210 | 1e-110 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
HMPBNJCG_00211 | 4e-21 | V | Glucan-binding protein C | |||
HMPBNJCG_00213 | 6.6e-122 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HMPBNJCG_00214 | 9.3e-236 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
HMPBNJCG_00215 | 7.5e-149 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
HMPBNJCG_00216 | 3.8e-42 | clcA_2 | P | chloride channel | ||
HMPBNJCG_00217 | 3.6e-40 | clcA_2 | P | chloride | ||
HMPBNJCG_00218 | 2.5e-43 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HMPBNJCG_00219 | 1.7e-48 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HMPBNJCG_00220 | 2.4e-130 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
HMPBNJCG_00221 | 3.8e-252 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HMPBNJCG_00222 | 3e-136 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
HMPBNJCG_00223 | 2.6e-105 | cps4C | M | biosynthesis protein | ||
HMPBNJCG_00224 | 5.3e-112 | cpsD | D | COG0489 ATPases involved in chromosome partitioning | ||
HMPBNJCG_00225 | 5.7e-250 | cpsE | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
HMPBNJCG_00226 | 8.5e-23 | rgpAc | GT4 | M | group 1 family protein | |
HMPBNJCG_00227 | 1.7e-27 | tnp | L | DDE domain | ||
HMPBNJCG_00228 | 2.2e-22 | L | Transposase | |||
HMPBNJCG_00229 | 3e-139 | L | Integrase core domain | |||
HMPBNJCG_00230 | 6.9e-96 | 2.7.8.12 | GT2 | S | Glycosyltransferase like family 2 | |
HMPBNJCG_00233 | 2.6e-143 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HMPBNJCG_00234 | 4.1e-118 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
HMPBNJCG_00235 | 9.4e-15 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
HMPBNJCG_00236 | 3.3e-19 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
HMPBNJCG_00237 | 6.6e-73 | dinF | V | Mate efflux family protein | ||
HMPBNJCG_00238 | 4.8e-41 | dinF | V | Mate efflux family protein | ||
HMPBNJCG_00240 | 2.3e-309 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
HMPBNJCG_00241 | 3.7e-190 | |||||
HMPBNJCG_00242 | 3.1e-89 | FNV0100 | F | Belongs to the Nudix hydrolase family | ||
HMPBNJCG_00243 | 3.5e-28 | 3.4.13.21 | I | Protein conserved in bacteria | ||
HMPBNJCG_00245 | 5.7e-118 | S | TraX protein | |||
HMPBNJCG_00246 | 1.3e-96 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
HMPBNJCG_00247 | 1.3e-148 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
HMPBNJCG_00248 | 3.2e-175 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HMPBNJCG_00249 | 4.7e-143 | 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 | ||
HMPBNJCG_00250 | 3.7e-54 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HMPBNJCG_00251 | 6.8e-133 | cas6 | S | Pfam:DUF2276 | ||
HMPBNJCG_00252 | 0.0 | csm1 | S | CRISPR-associated protein Csm1 family | ||
HMPBNJCG_00253 | 5.6e-62 | csm2 | L | Pfam:DUF310 | ||
HMPBNJCG_00254 | 1.1e-116 | csm3 | L | RAMP superfamily | ||
HMPBNJCG_00255 | 5.8e-166 | csm4 | L | CRISPR-associated RAMP protein, Csm4 family | ||
HMPBNJCG_00256 | 4.4e-205 | csm5 | L | CRISPR-associated RAMP protein, Csm5 family | ||
HMPBNJCG_00257 | 2.1e-14 | csm6 | S | Psort location Cytoplasmic, score | ||
HMPBNJCG_00258 | 5.2e-74 | csm6 | S | Psort location Cytoplasmic, score | ||
HMPBNJCG_00259 | 7e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
HMPBNJCG_00260 | 7.5e-112 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
HMPBNJCG_00261 | 1.2e-63 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
HMPBNJCG_00263 | 2.5e-267 | dtpT | E | transporter | ||
HMPBNJCG_00264 | 1e-103 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
HMPBNJCG_00265 | 8.8e-134 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HMPBNJCG_00266 | 1.8e-67 | yecS | P | ABC transporter (Permease | ||
HMPBNJCG_00268 | 8.1e-114 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
HMPBNJCG_00269 | 9.8e-35 | 3.1.3.6, 3.1.4.16 | F | nucleotide catabolic process | ||
HMPBNJCG_00270 | 5.4e-104 | yfiF3 | K | sequence-specific DNA binding | ||
HMPBNJCG_00271 | 1.9e-147 | L | Transposase | |||
HMPBNJCG_00272 | 1.6e-247 | 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 | ||
HMPBNJCG_00273 | 1.8e-240 | agcS | E | (Alanine) symporter | ||
HMPBNJCG_00274 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HMPBNJCG_00275 | 4.6e-241 | metY | 2.5.1.49 | E | o-acetylhomoserine | |
HMPBNJCG_00276 | 1.8e-59 | Q | phosphatase activity | |||
HMPBNJCG_00277 | 9.3e-62 | S | haloacid dehalogenase-like hydrolase | |||
HMPBNJCG_00278 | 3.5e-88 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
HMPBNJCG_00279 | 1.1e-110 | hsdS2 | 2.1.1.72 | V | Type I restriction modification DNA specificity domain | |
HMPBNJCG_00280 | 1.7e-96 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
HMPBNJCG_00281 | 2.6e-49 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
HMPBNJCG_00282 | 4.9e-151 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HMPBNJCG_00283 | 5.3e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
HMPBNJCG_00284 | 1.4e-71 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
HMPBNJCG_00285 | 1.9e-43 | yktA | S | Belongs to the UPF0223 family | ||
HMPBNJCG_00286 | 5e-142 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
HMPBNJCG_00287 | 3e-256 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
HMPBNJCG_00288 | 3.3e-158 | pstS | P | phosphate | ||
HMPBNJCG_00289 | 1.8e-154 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HMPBNJCG_00290 | 2e-155 | pstA | P | phosphate transport system permease | ||
HMPBNJCG_00291 | 5.2e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
HMPBNJCG_00292 | 1.7e-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 | |
HMPBNJCG_00293 | 2.4e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HMPBNJCG_00294 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
HMPBNJCG_00295 | 7e-195 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
HMPBNJCG_00296 | 1.3e-187 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
HMPBNJCG_00297 | 1.1e-17 | |||||
HMPBNJCG_00298 | 3.7e-09 | |||||
HMPBNJCG_00299 | 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 |
HMPBNJCG_00300 | 3.4e-304 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
HMPBNJCG_00301 | 2.3e-23 | L | Transposase | |||
HMPBNJCG_00302 | 4.6e-25 | tatA | U | protein secretion | ||
HMPBNJCG_00303 | 5.8e-121 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
HMPBNJCG_00304 | 1.1e-300 | ywbL | P | COG0672 High-affinity Fe2 Pb2 permease | ||
HMPBNJCG_00305 | 5.6e-233 | ycdB | P | peroxidase | ||
HMPBNJCG_00306 | 7.1e-153 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
HMPBNJCG_00307 | 3e-34 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00308 | 3.7e-85 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00309 | 1.7e-60 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00310 | 1.5e-65 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00311 | 2.4e-134 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00312 | 1.9e-37 | 3.5.1.28 | NU | amidase activity | ||
HMPBNJCG_00313 | 8.5e-266 | 3.5.1.28 | NU | amidase activity | ||
HMPBNJCG_00314 | 3.6e-82 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
HMPBNJCG_00315 | 2.6e-20 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
HMPBNJCG_00316 | 0.0 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
HMPBNJCG_00317 | 1.8e-198 | acoC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
HMPBNJCG_00318 | 3.7e-182 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
HMPBNJCG_00319 | 6e-185 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
HMPBNJCG_00320 | 5e-38 | P | membrane protein (DUF2207) | |||
HMPBNJCG_00321 | 2.8e-65 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
HMPBNJCG_00322 | 3.7e-235 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HMPBNJCG_00323 | 2.9e-127 | 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 | |
HMPBNJCG_00324 | 8.6e-218 | yeaB | K | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
HMPBNJCG_00325 | 1.2e-157 | rssA | S | Phospholipase, patatin family | ||
HMPBNJCG_00326 | 3.9e-78 | estA | E | GDSL-like protein | ||
HMPBNJCG_00327 | 2.6e-15 | estA | E | Lysophospholipase L1 and related esterases | ||
HMPBNJCG_00328 | 3.7e-293 | S | unusual protein kinase | |||
HMPBNJCG_00329 | 4.9e-39 | S | granule-associated protein | |||
HMPBNJCG_00330 | 7.9e-138 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HMPBNJCG_00331 | 5.8e-28 | bglH | 3.2.1.86 | GT1 | G | beta-glucosidase activity |
HMPBNJCG_00332 | 1.3e-199 | S | hmm pf01594 | |||
HMPBNJCG_00333 | 1.6e-44 | G | alpha-ribazole phosphatase activity | |||
HMPBNJCG_00334 | 2e-33 | G | Belongs to the phosphoglycerate mutase family | |||
HMPBNJCG_00335 | 1.1e-25 | G | Belongs to the phosphoglycerate mutase family | |||
HMPBNJCG_00336 | 8.8e-66 | pgm | G | Belongs to the phosphoglycerate mutase family | ||
HMPBNJCG_00337 | 1.7e-80 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
HMPBNJCG_00338 | 4.9e-94 | V | VanZ like family | |||
HMPBNJCG_00339 | 2.1e-203 | 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 | |
HMPBNJCG_00340 | 4.2e-175 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HMPBNJCG_00341 | 3.2e-295 | 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 | |
HMPBNJCG_00342 | 1.6e-88 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
HMPBNJCG_00343 | 1.9e-164 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
HMPBNJCG_00344 | 1.2e-19 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
HMPBNJCG_00346 | 7.7e-35 | |||||
HMPBNJCG_00349 | 7.8e-202 | S | Phage integrase family | |||
HMPBNJCG_00351 | 8.5e-57 | 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 | ||
HMPBNJCG_00352 | 4.3e-133 | XK27_05110 | P | chloride | ||
HMPBNJCG_00353 | 1.2e-61 | XK27_05110 | P | chloride | ||
HMPBNJCG_00354 | 8.7e-41 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
HMPBNJCG_00355 | 1.3e-282 | clcA | P | Chloride transporter, ClC family | ||
HMPBNJCG_00356 | 6.7e-75 | fld | C | Flavodoxin | ||
HMPBNJCG_00358 | 4.7e-126 | XK27_08875 | O | Zinc-dependent metalloprotease | ||
HMPBNJCG_00359 | 3.5e-151 | estA | CE1 | S | Putative esterase | |
HMPBNJCG_00360 | 1e-309 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HMPBNJCG_00361 | 1.2e-135 | XK27_08845 | S | abc transporter atp-binding protein | ||
HMPBNJCG_00362 | 4e-148 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
HMPBNJCG_00363 | 3.3e-178 | XK27_08835 | S | ABC transporter substrate binding protein | ||
HMPBNJCG_00364 | 3.2e-17 | S | Domain of unknown function (DUF4649) | |||
HMPBNJCG_00366 | 6.9e-30 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
HMPBNJCG_00367 | 1.1e-22 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
HMPBNJCG_00368 | 3.2e-09 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
HMPBNJCG_00371 | 1.3e-57 | T | Toxic component of a toxin-antitoxin (TA) module | |||
HMPBNJCG_00373 | 8.2e-70 | argR | K | Regulates arginine biosynthesis genes | ||
HMPBNJCG_00374 | 1e-57 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
HMPBNJCG_00375 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HMPBNJCG_00376 | 7e-34 | S | Protein of unknown function (DUF3021) | |||
HMPBNJCG_00377 | 1.2e-61 | KT | phosphorelay signal transduction system | |||
HMPBNJCG_00379 | 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 | ||
HMPBNJCG_00381 | 7.8e-103 | 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 | |
HMPBNJCG_00382 | 6.4e-107 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
HMPBNJCG_00383 | 1e-232 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
HMPBNJCG_00384 | 2.8e-197 | 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 | ||
HMPBNJCG_00385 | 2.3e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
HMPBNJCG_00386 | 1.3e-276 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HMPBNJCG_00387 | 1.2e-188 | 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 | |
HMPBNJCG_00388 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
HMPBNJCG_00389 | 1.4e-152 | sua5 | 2.7.7.87 | J | Belongs to the SUA5 family | |
HMPBNJCG_00390 | 3.1e-112 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
HMPBNJCG_00391 | 6.8e-275 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
HMPBNJCG_00392 | 2.5e-43 | ysdA | L | Membrane | ||
HMPBNJCG_00393 | 6.6e-190 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
HMPBNJCG_00394 | 3.4e-291 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
HMPBNJCG_00395 | 3e-130 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HMPBNJCG_00396 | 3.6e-179 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
HMPBNJCG_00398 | 2.8e-39 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
HMPBNJCG_00399 | 1.7e-83 | ypmS | S | Protein conserved in bacteria | ||
HMPBNJCG_00400 | 6e-144 | ypmR | E | lipolytic protein G-D-S-L family | ||
HMPBNJCG_00401 | 1e-148 | DegV | S | DegV family | ||
HMPBNJCG_00402 | 5.8e-305 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HMPBNJCG_00403 | 1.8e-72 | argR | K | Regulates arginine biosynthesis genes | ||
HMPBNJCG_00404 | 5e-159 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HMPBNJCG_00405 | 3e-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 | |
HMPBNJCG_00406 | 3.5e-29 | xseB | 3.1.11.6 | L | exodeoxyribonuclease VII activity | |
HMPBNJCG_00407 | 1.2e-247 | 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 | |
HMPBNJCG_00410 | 3.4e-120 | 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 | |
HMPBNJCG_00411 | 2.9e-125 | dnaD | ||||
HMPBNJCG_00412 | 9.3e-183 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
HMPBNJCG_00413 | 2e-94 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
HMPBNJCG_00414 | 0.0 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
HMPBNJCG_00415 | 6.7e-139 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
HMPBNJCG_00416 | 9.2e-175 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
HMPBNJCG_00417 | 4.2e-118 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
HMPBNJCG_00418 | 7.1e-223 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HMPBNJCG_00419 | 1.6e-239 | rodA | D | Belongs to the SEDS family | ||
HMPBNJCG_00420 | 4.5e-49 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
HMPBNJCG_00421 | 5.5e-61 | 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 | |
HMPBNJCG_00422 | 1.9e-133 | 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 | |
HMPBNJCG_00423 | 5e-128 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
HMPBNJCG_00424 | 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 | ||
HMPBNJCG_00425 | 1.5e-106 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
HMPBNJCG_00426 | 1.1e-234 | 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 | |
HMPBNJCG_00427 | 2.3e-116 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
HMPBNJCG_00428 | 5.7e-183 | 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 | |
HMPBNJCG_00429 | 2.1e-196 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
HMPBNJCG_00431 | 4.2e-86 | L | Integrase core domain protein | |||
HMPBNJCG_00432 | 1.1e-53 | L | transposition | |||
HMPBNJCG_00433 | 8.2e-22 | L | Transposase | |||
HMPBNJCG_00434 | 5.2e-36 | L | transposase activity | |||
HMPBNJCG_00435 | 1.3e-22 | XK27_08085 | ||||
HMPBNJCG_00436 | 5.6e-92 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
HMPBNJCG_00437 | 2.3e-09 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
HMPBNJCG_00438 | 2e-140 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
HMPBNJCG_00439 | 1.1e-121 | ylfI | S | tigr01906 | ||
HMPBNJCG_00440 | 5.9e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HMPBNJCG_00441 | 1.5e-143 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
HMPBNJCG_00442 | 4.1e-217 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
HMPBNJCG_00445 | 1.9e-205 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HMPBNJCG_00446 | 8.3e-113 | rmlC | 1.1.1.133, 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 | |
HMPBNJCG_00447 | 1.9e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HMPBNJCG_00448 | 1.1e-206 | yurR | 1.4.5.1 | E | oxidoreductase | |
HMPBNJCG_00449 | 5.7e-102 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
HMPBNJCG_00450 | 9.6e-149 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
HMPBNJCG_00451 | 2.7e-123 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
HMPBNJCG_00452 | 1.7e-70 | gtrA | S | GtrA-like protein | ||
HMPBNJCG_00453 | 1.5e-250 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HMPBNJCG_00454 | 6e-169 | ybbR | S | Protein conserved in bacteria | ||
HMPBNJCG_00455 | 5.6e-124 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
HMPBNJCG_00456 | 7.5e-255 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
HMPBNJCG_00457 | 8.7e-150 | cobQ | S | glutamine amidotransferase | ||
HMPBNJCG_00458 | 0.0 | mprF | 2.3.2.3 | J | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
HMPBNJCG_00459 | 2.2e-131 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
HMPBNJCG_00460 | 0.0 | uup | S | abc transporter atp-binding protein | ||
HMPBNJCG_00461 | 2.1e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
HMPBNJCG_00462 | 2.1e-178 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
HMPBNJCG_00463 | 2.1e-28 | 6.3.2.2, 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | ||
HMPBNJCG_00464 | 8.6e-265 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
HMPBNJCG_00465 | 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) | |
HMPBNJCG_00466 | 7.9e-39 | ptsH | G | phosphocarrier protein Hpr | ||
HMPBNJCG_00467 | 3.3e-222 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
HMPBNJCG_00468 | 5.1e-212 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
HMPBNJCG_00469 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
HMPBNJCG_00470 | 2.2e-34 | nrdH | O | Glutaredoxin | ||
HMPBNJCG_00471 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HMPBNJCG_00472 | 1.7e-184 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HMPBNJCG_00474 | 4.2e-71 | L | Transposase (IS116 IS110 IS902 family) | |||
HMPBNJCG_00475 | 3.3e-26 | L | Transposase (IS116 IS110 IS902 family) | |||
HMPBNJCG_00476 | 1.2e-164 | ypuA | S | secreted protein | ||
HMPBNJCG_00477 | 1.1e-55 | yaeR | E | COG0346 LactoylglutaTHIone lyase and related lyases | ||
HMPBNJCG_00478 | 5.1e-131 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
HMPBNJCG_00479 | 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 | |
HMPBNJCG_00480 | 1.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HMPBNJCG_00481 | 3.4e-258 | noxE | P | NADH oxidase | ||
HMPBNJCG_00482 | 1.9e-294 | yfmM | S | abc transporter atp-binding protein | ||
HMPBNJCG_00483 | 3.3e-82 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
HMPBNJCG_00484 | 8.7e-85 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
HMPBNJCG_00485 | 4.5e-44 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
HMPBNJCG_00486 | 2e-86 | S | ECF-type riboflavin transporter, S component | |||
HMPBNJCG_00488 | 5e-240 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
HMPBNJCG_00489 | 2e-55 | nrdD_1 | 1.1.98.6, 1.17.4.1 | F | Ribonucleoside-triphosphate reductase | |
HMPBNJCG_00492 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HMPBNJCG_00493 | 9.9e-94 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
HMPBNJCG_00494 | 1.1e-197 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HMPBNJCG_00495 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
HMPBNJCG_00496 | 8.4e-125 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
HMPBNJCG_00497 | 6.6e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HMPBNJCG_00498 | 1.1e-198 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
HMPBNJCG_00499 | 2.4e-92 | pat | 2.3.1.183 | M | acetyltransferase | |
HMPBNJCG_00500 | 9e-278 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HMPBNJCG_00501 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
HMPBNJCG_00502 | 3.1e-127 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
HMPBNJCG_00503 | 1.2e-62 | bioY | S | biotin transmembrane transporter activity | ||
HMPBNJCG_00504 | 9.8e-88 | proW | P | Binding-protein-dependent transport system inner membrane component | ||
HMPBNJCG_00505 | 1.5e-138 | proV | E | abc transporter atp-binding protein | ||
HMPBNJCG_00506 | 4.4e-169 | proX | M | ABC transporter, substrate-binding protein, QAT family | ||
HMPBNJCG_00507 | 3e-111 | proWZ | P | ABC transporter (Permease | ||
HMPBNJCG_00508 | 1.2e-280 | hutH | 4.3.1.3 | E | Histidine ammonia-lyase | |
HMPBNJCG_00509 | 1.6e-205 | S | Protein of unknown function (DUF917) | |||
HMPBNJCG_00510 | 1.3e-309 | hutU | 4.2.1.49 | E | Catalyzes the conversion of urocanate to 4-imidazolone- 5-propionate | |
HMPBNJCG_00511 | 1.6e-59 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
HMPBNJCG_00512 | 4.4e-101 | desR | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
HMPBNJCG_00513 | 1.5e-192 | desK | 2.7.13.3 | T | Histidine kinase | |
HMPBNJCG_00514 | 1.4e-133 | yvfS | V | ABC-2 type transporter | ||
HMPBNJCG_00515 | 8.7e-159 | XK27_09825 | V | abc transporter atp-binding protein | ||
HMPBNJCG_00518 | 8.1e-163 | yocS | S | Transporter | ||
HMPBNJCG_00519 | 1.2e-82 | cdd | 2.4.2.4, 3.5.4.5 | F | cytidine deaminase activity | |
HMPBNJCG_00520 | 7.5e-115 | yvfS | V | Transporter | ||
HMPBNJCG_00521 | 3.9e-151 | XK27_09825 | V | abc transporter atp-binding protein | ||
HMPBNJCG_00522 | 2.7e-14 | liaI | KT | membrane | ||
HMPBNJCG_00523 | 2.6e-30 | liaI | KT | membrane | ||
HMPBNJCG_00524 | 6e-99 | XK27_05000 | S | Fe-S-cluster oxidoreductase | ||
HMPBNJCG_00525 | 0.0 | V | ABC transporter (permease) | |||
HMPBNJCG_00526 | 1.9e-133 | macB2 | V | ABC transporter, ATP-binding protein | ||
HMPBNJCG_00527 | 3.1e-165 | T | Histidine kinase | |||
HMPBNJCG_00528 | 4.6e-123 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HMPBNJCG_00529 | 2e-77 | 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 | |
HMPBNJCG_00530 | 3.3e-69 | pbuX | F | xanthine permease | ||
HMPBNJCG_00531 | 9.2e-119 | pbuX | F | xanthine permease | ||
HMPBNJCG_00532 | 1.5e-247 | norM | V | Multidrug efflux pump | ||
HMPBNJCG_00533 | 4.3e-188 | 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 | |
HMPBNJCG_00534 | 1.3e-235 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
HMPBNJCG_00535 | 9.4e-65 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HMPBNJCG_00536 | 8.2e-57 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HMPBNJCG_00537 | 4.8e-25 | csbD | K | CsbD-like | ||
HMPBNJCG_00538 | 6.2e-228 | yfnA | E | amino acid | ||
HMPBNJCG_00539 | 5.1e-110 | XK27_02070 | S | nitroreductase | ||
HMPBNJCG_00540 | 9.5e-150 | 1.13.11.2 | S | glyoxalase | ||
HMPBNJCG_00541 | 5.6e-77 | ywnA | K | Transcriptional regulator | ||
HMPBNJCG_00542 | 9.5e-158 | E | Alpha/beta hydrolase of unknown function (DUF915) | |||
HMPBNJCG_00543 | 1.9e-231 | 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 | ||
HMPBNJCG_00544 | 1.4e-110 | drgA | C | Nitroreductase | ||
HMPBNJCG_00545 | 3e-102 | yoaK | S | Protein of unknown function (DUF1275) | ||
HMPBNJCG_00547 | 6.8e-161 | yvgN | C | reductase | ||
HMPBNJCG_00548 | 1.7e-179 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HMPBNJCG_00549 | 3.6e-282 | XK27_07020 | S | Belongs to the UPF0371 family | ||
HMPBNJCG_00551 | 1.1e-37 | BP1961 | P | nitric oxide dioxygenase activity | ||
HMPBNJCG_00552 | 1.4e-54 | K | response regulator | |||
HMPBNJCG_00553 | 9.3e-72 | S | Signal peptide protein, YSIRK family | |||
HMPBNJCG_00555 | 4.5e-61 | |||||
HMPBNJCG_00556 | 1.8e-270 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HMPBNJCG_00557 | 1e-137 | |||||
HMPBNJCG_00558 | 5.3e-12 | IQ | PFAM AMP-dependent synthetase and ligase | |||
HMPBNJCG_00559 | 2.7e-12 | IQ | PFAM AMP-dependent synthetase and ligase | |||
HMPBNJCG_00560 | 5.8e-109 | MA20_06410 | E | LysE type translocator | ||
HMPBNJCG_00561 | 5.6e-08 | |||||
HMPBNJCG_00562 | 2.7e-09 | |||||
HMPBNJCG_00563 | 0.0 | M | family 8 | |||
HMPBNJCG_00565 | 1.5e-162 | hrtB | V | MacB-like periplasmic core domain | ||
HMPBNJCG_00566 | 3.1e-116 | devA | 3.6.3.25 | V | abc transporter atp-binding protein | |
HMPBNJCG_00567 | 1.1e-151 | V | MatE | |||
HMPBNJCG_00569 | 3.9e-110 | C | Fe-S oxidoreductases | |||
HMPBNJCG_00570 | 1.2e-176 | EGP | Major Facilitator Superfamily | |||
HMPBNJCG_00571 | 5.5e-258 | I | radical SAM domain protein | |||
HMPBNJCG_00573 | 6.5e-159 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
HMPBNJCG_00574 | 1.4e-150 | L | Integrase core domain protein | |||
HMPBNJCG_00575 | 1.8e-87 | L | transposase activity | |||
HMPBNJCG_00577 | 2.8e-85 | |||||
HMPBNJCG_00578 | 0.0 | sbcC | L | ATPase involved in DNA repair | ||
HMPBNJCG_00579 | 6.9e-231 | 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 | ||
HMPBNJCG_00580 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
HMPBNJCG_00581 | 0.0 | lacS | G | transporter | ||
HMPBNJCG_00582 | 6.4e-201 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
HMPBNJCG_00583 | 6.6e-195 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HMPBNJCG_00584 | 4e-289 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
HMPBNJCG_00585 | 1.6e-221 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
HMPBNJCG_00586 | 2.3e-184 | galR | K | Transcriptional regulator | ||
HMPBNJCG_00587 | 2.7e-08 | L | Integrase core domain protein | |||
HMPBNJCG_00588 | 1.2e-25 | L | transposition | |||
HMPBNJCG_00589 | 3.5e-228 | zmpB | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
HMPBNJCG_00590 | 6.7e-17 | rtxA | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
HMPBNJCG_00591 | 2.5e-101 | V | abc transporter atp-binding protein | |||
HMPBNJCG_00592 | 4.3e-40 | V | abc transporter atp-binding protein | |||
HMPBNJCG_00593 | 0.0 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
HMPBNJCG_00594 | 6.4e-62 | L | Transposase | |||
HMPBNJCG_00595 | 7e-150 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00596 | 1.8e-33 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00597 | 1.7e-120 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00598 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HMPBNJCG_00599 | 5.9e-188 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
HMPBNJCG_00600 | 1.4e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HMPBNJCG_00601 | 5.8e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
HMPBNJCG_00604 | 2.2e-114 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
HMPBNJCG_00605 | 5.8e-175 | vraS | 2.7.13.3 | T | Histidine kinase | |
HMPBNJCG_00606 | 3.7e-120 | yvqF | KT | membrane | ||
HMPBNJCG_00607 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
HMPBNJCG_00608 | 2e-132 | stp | 3.1.3.16 | T | phosphatase | |
HMPBNJCG_00609 | 4.4e-247 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HMPBNJCG_00610 | 2.5e-172 | 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 | |
HMPBNJCG_00611 | 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 | ||
HMPBNJCG_00612 | 2.7e-46 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
HMPBNJCG_00613 | 9.8e-112 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
HMPBNJCG_00614 | 2.8e-212 | 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) | ||
HMPBNJCG_00615 | 3.4e-149 | XK27_02985 | S | overlaps another CDS with the same product name | ||
HMPBNJCG_00616 | 2.1e-148 | supH | S | overlaps another CDS with the same product name | ||
HMPBNJCG_00617 | 8.6e-63 | yvoA_1 | K | Transcriptional | ||
HMPBNJCG_00618 | 2.8e-120 | skfE | V | abc transporter atp-binding protein | ||
HMPBNJCG_00619 | 3.3e-133 | V | ATPase activity | |||
HMPBNJCG_00620 | 4.3e-172 | oppF | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_00621 | 2.2e-204 | oppD | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_00622 | 4.9e-168 | amiD | P | ABC transporter (Permease | ||
HMPBNJCG_00623 | 4.2e-278 | amiC | P | ABC transporter (Permease | ||
HMPBNJCG_00624 | 3.7e-140 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HMPBNJCG_00625 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HMPBNJCG_00626 | 8.1e-45 | L | Transposase | |||
HMPBNJCG_00627 | 4.1e-158 | L | COG2801 Transposase and inactivated derivatives | |||
HMPBNJCG_00628 | 1.2e-24 | oppF | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_00629 | 3.8e-45 | oppF | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_00630 | 1.4e-40 | tatD | L | Hydrolase, tatd | ||
HMPBNJCG_00631 | 6.7e-218 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
HMPBNJCG_00632 | 1e-110 | L | Integrase core domain protein | |||
HMPBNJCG_00633 | 1.1e-23 | L | transposase activity | |||
HMPBNJCG_00634 | 8.9e-18 | L | transposase activity | |||
HMPBNJCG_00635 | 1.4e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HMPBNJCG_00636 | 9.8e-174 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HMPBNJCG_00637 | 5.4e-150 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
HMPBNJCG_00638 | 5.5e-121 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
HMPBNJCG_00639 | 1.5e-103 | yjbK | S | Adenylate cyclase | ||
HMPBNJCG_00640 | 2.1e-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) | |
HMPBNJCG_00641 | 7e-206 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
HMPBNJCG_00642 | 2e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
HMPBNJCG_00643 | 5.7e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HMPBNJCG_00644 | 1.6e-131 | puuD | T | peptidase C26 | ||
HMPBNJCG_00645 | 6.2e-120 | radC | E | Belongs to the UPF0758 family | ||
HMPBNJCG_00646 | 4.9e-272 | rgpF | M | Rhamnan synthesis protein F | ||
HMPBNJCG_00647 | 9e-223 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
HMPBNJCG_00648 | 6.4e-140 | rgpC | GM | Transport permease protein | ||
HMPBNJCG_00649 | 2e-169 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
HMPBNJCG_00650 | 1.1e-222 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
HMPBNJCG_00651 | 5e-174 | S | Glucosyl transferase GtrII | |||
HMPBNJCG_00652 | 1.8e-28 | S | Glucosyl transferase GtrII | |||
HMPBNJCG_00653 | 1.6e-219 | GT4 | M | transferase activity, transferring glycosyl groups | ||
HMPBNJCG_00654 | 2e-217 | M | Psort location CytoplasmicMembrane, score | |||
HMPBNJCG_00655 | 0.0 | rgpF | GT2,GT4 | M | Glycosyltransferase like family 2 | |
HMPBNJCG_00656 | 5.9e-151 | 2.4.1.60 | S | Glycosyltransferase group 2 family protein | ||
HMPBNJCG_00657 | 4.6e-42 | S | Uncharacterized conserved protein (DUF2304) | |||
HMPBNJCG_00658 | 3.8e-128 | arnC | M | group 2 family protein | ||
HMPBNJCG_00659 | 1.1e-181 | cpsIaJ | S | Glycosyltransferase like family 2 | ||
HMPBNJCG_00660 | 1e-184 | S | Glycosyltransferase like family 2 | |||
HMPBNJCG_00661 | 9.4e-223 | amrA | S | membrane protein involved in the export of O-antigen and teichoic acid | ||
HMPBNJCG_00662 | 1.5e-160 | 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 | |
HMPBNJCG_00663 | 2.9e-235 | S | Predicted membrane protein (DUF2142) | |||
HMPBNJCG_00664 | 1.7e-173 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
HMPBNJCG_00665 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
HMPBNJCG_00666 | 1.1e-201 | 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 | ||
HMPBNJCG_00667 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HMPBNJCG_00668 | 5.5e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HMPBNJCG_00669 | 1.1e-136 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HMPBNJCG_00670 | 2.1e-202 | arcT | 2.6.1.1 | E | Aminotransferase | |
HMPBNJCG_00671 | 9.4e-136 | ET | ABC transporter | |||
HMPBNJCG_00672 | 1.1e-142 | ET | Belongs to the bacterial solute-binding protein 3 family | |||
HMPBNJCG_00673 | 2.9e-84 | mutT | 3.6.1.55 | F | Nudix family | |
HMPBNJCG_00674 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
HMPBNJCG_00676 | 1.2e-55 | V | CAAX protease self-immunity | |||
HMPBNJCG_00677 | 2.6e-32 | S | CAAX amino terminal protease family protein | |||
HMPBNJCG_00678 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
HMPBNJCG_00679 | 1e-136 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HMPBNJCG_00680 | 2.4e-16 | XK27_00735 | ||||
HMPBNJCG_00681 | 1.4e-248 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
HMPBNJCG_00683 | 7.3e-135 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HMPBNJCG_00686 | 5.5e-65 | paaI | Q | protein possibly involved in aromatic compounds catabolism | ||
HMPBNJCG_00687 | 6.6e-30 | ycaO | O | OsmC-like protein | ||
HMPBNJCG_00689 | 1.7e-154 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
HMPBNJCG_00691 | 5.6e-110 | csn2 | S | CRISPR-associated protein (Cas_Csn2) | ||
HMPBNJCG_00692 | 3.5e-52 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HMPBNJCG_00693 | 1.5e-163 | 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 | ||
HMPBNJCG_00694 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
HMPBNJCG_00695 | 6.7e-116 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
HMPBNJCG_00696 | 3.2e-298 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
HMPBNJCG_00697 | 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 | |
HMPBNJCG_00698 | 2.6e-109 | 3.1.3.18 | S | IA, variant 1 | ||
HMPBNJCG_00699 | 2.2e-117 | lrgB | M | effector of murein hydrolase | ||
HMPBNJCG_00700 | 2.2e-58 | lrgA | S | Effector of murein hydrolase LrgA | ||
HMPBNJCG_00702 | 5.4e-59 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
HMPBNJCG_00703 | 1.5e-52 | ogt | 2.1.1.63, 3.2.2.20 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
HMPBNJCG_00704 | 7e-220 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HMPBNJCG_00705 | 3.9e-104 | wecD | M | Acetyltransferase GNAT family | ||
HMPBNJCG_00706 | 1.3e-209 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
HMPBNJCG_00707 | 5.1e-96 | GK | ROK family | |||
HMPBNJCG_00708 | 8.1e-72 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
HMPBNJCG_00709 | 1.7e-47 | XK27_08050 | O | stress-induced mitochondrial fusion | ||
HMPBNJCG_00710 | 1.3e-19 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
HMPBNJCG_00711 | 2.3e-206 | potD | P | spermidine putrescine ABC transporter | ||
HMPBNJCG_00712 | 3e-134 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
HMPBNJCG_00713 | 3.7e-140 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
HMPBNJCG_00714 | 1.2e-213 | 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 | |
HMPBNJCG_00715 | 7.8e-171 | murB | 1.3.1.98 | M | cell wall formation | |
HMPBNJCG_00716 | 2.9e-87 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
HMPBNJCG_00717 | 1.2e-61 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
HMPBNJCG_00718 | 1.2e-298 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HMPBNJCG_00719 | 7e-147 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
HMPBNJCG_00720 | 1e-99 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
HMPBNJCG_00721 | 0.0 | ydaO | E | amino acid | ||
HMPBNJCG_00722 | 1.1e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HMPBNJCG_00723 | 4.1e-37 | ylqC | L | Belongs to the UPF0109 family | ||
HMPBNJCG_00724 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HMPBNJCG_00725 | 6.9e-172 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
HMPBNJCG_00726 | 8.2e-159 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HMPBNJCG_00727 | 2.1e-74 | S | QueT transporter | |||
HMPBNJCG_00728 | 1.9e-55 | L | Transposase | |||
HMPBNJCG_00729 | 5.7e-186 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
HMPBNJCG_00730 | 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 | |
HMPBNJCG_00731 | 3.7e-85 | ccl | S | cog cog4708 | ||
HMPBNJCG_00732 | 7.4e-164 | rbn | E | Belongs to the UPF0761 family | ||
HMPBNJCG_00733 | 1.5e-166 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
HMPBNJCG_00734 | 3.3e-231 | ytoI | K | transcriptional regulator containing CBS domains | ||
HMPBNJCG_00735 | 2.4e-98 | XK27_07830 | 2.3.1.128 | J | Acetyltransferase GNAT Family | |
HMPBNJCG_00736 | 1e-232 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HMPBNJCG_00737 | 0.0 | comEC | S | Competence protein ComEC | ||
HMPBNJCG_00738 | 2.2e-96 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
HMPBNJCG_00739 | 1.3e-142 | plsC | 2.3.1.51 | I | Acyltransferase | |
HMPBNJCG_00740 | 1.7e-77 | nodB3 | G | polysaccharide deacetylase | ||
HMPBNJCG_00741 | 4.1e-22 | nodB3 | G | polysaccharide deacetylase | ||
HMPBNJCG_00742 | 2.3e-139 | yabB | 2.1.1.223 | L | Methyltransferase | |
HMPBNJCG_00743 | 1e-41 | yazA | L | endonuclease containing a URI domain | ||
HMPBNJCG_00744 | 3.2e-252 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
HMPBNJCG_00745 | 2.3e-154 | corA | P | CorA-like protein | ||
HMPBNJCG_00746 | 1.9e-62 | yjqA | S | Bacterial PH domain | ||
HMPBNJCG_00747 | 7.8e-100 | thiT | S | Thiamine transporter | ||
HMPBNJCG_00748 | 2.1e-157 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
HMPBNJCG_00749 | 1.9e-201 | yjbB | G | Permeases of the major facilitator superfamily | ||
HMPBNJCG_00750 | 3.1e-300 | 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 | ||
HMPBNJCG_00751 | 1.4e-121 | ywaF | S | Integral membrane protein (intg_mem_TP0381) | ||
HMPBNJCG_00752 | 3e-259 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HMPBNJCG_00756 | 1.1e-155 | cjaA | ET | ABC transporter substrate-binding protein | ||
HMPBNJCG_00757 | 1.7e-134 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HMPBNJCG_00758 | 3e-106 | P | ABC transporter (Permease | |||
HMPBNJCG_00759 | 6e-115 | papP | P | ABC transporter (Permease | ||
HMPBNJCG_00760 | 1.7e-193 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HMPBNJCG_00761 | 4.7e-31 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
HMPBNJCG_00762 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
HMPBNJCG_00763 | 2.7e-73 | copY | K | Copper transport repressor, CopY TcrY family | ||
HMPBNJCG_00764 | 2.1e-143 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
HMPBNJCG_00765 | 1.1e-228 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
HMPBNJCG_00766 | 3.3e-98 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
HMPBNJCG_00767 | 2.5e-133 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
HMPBNJCG_00768 | 7.8e-180 | 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) | |
HMPBNJCG_00769 | 8e-105 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
HMPBNJCG_00770 | 2.8e-257 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
HMPBNJCG_00771 | 3.7e-42 | pchB | 2.5.1.19, 4.2.1.10, 4.2.99.21, 5.4.99.5 | E | Chorismate mutase | |
HMPBNJCG_00772 | 3.2e-56 | |||||
HMPBNJCG_00773 | 0.0 | ctpE | P | E1-E2 ATPase | ||
HMPBNJCG_00774 | 2e-25 | |||||
HMPBNJCG_00775 | 1.2e-43 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
HMPBNJCG_00776 | 9.7e-28 | L | transposase activity | |||
HMPBNJCG_00777 | 2.7e-129 | K | transcriptional regulator, MerR family | |||
HMPBNJCG_00778 | 1.4e-104 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HMPBNJCG_00779 | 1.2e-41 | WQ51_02910 | S | Protein of unknown function, DUF536 | ||
HMPBNJCG_00780 | 7.4e-64 | XK27_02560 | S | cog cog2151 | ||
HMPBNJCG_00781 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HMPBNJCG_00782 | 7.7e-227 | ytfP | S | Flavoprotein | ||
HMPBNJCG_00784 | 3.1e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HMPBNJCG_00785 | 1.2e-151 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
HMPBNJCG_00786 | 2.7e-183 | ecsB | U | ABC transporter | ||
HMPBNJCG_00787 | 2.3e-133 | ecsA | V | abc transporter atp-binding protein | ||
HMPBNJCG_00788 | 3.9e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
HMPBNJCG_00789 | 5.6e-12 | |||||
HMPBNJCG_00790 | 2.6e-55 | S | CD20-like family | |||
HMPBNJCG_00791 | 2.1e-106 | |||||
HMPBNJCG_00793 | 0.0 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
HMPBNJCG_00794 | 5.8e-126 | ylbM | S | Belongs to the UPF0348 family | ||
HMPBNJCG_00795 | 2e-140 | yqeM | Q | Methyltransferase domain protein | ||
HMPBNJCG_00796 | 6e-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 | ||
HMPBNJCG_00797 | 1.4e-107 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
HMPBNJCG_00798 | 3.1e-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) | |
HMPBNJCG_00799 | 3.5e-49 | yhbY | J | RNA-binding protein | ||
HMPBNJCG_00800 | 1.7e-215 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
HMPBNJCG_00801 | 1.8e-98 | yqeG | S | hydrolase of the HAD superfamily | ||
HMPBNJCG_00802 | 2.6e-153 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
HMPBNJCG_00803 | 1.3e-57 | |||||
HMPBNJCG_00804 | 2.3e-273 | 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) | |
HMPBNJCG_00805 | 3.5e-269 | 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) | |
HMPBNJCG_00806 | 1.4e-47 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HMPBNJCG_00807 | 6.3e-31 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
HMPBNJCG_00808 | 1e-148 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HMPBNJCG_00809 | 5.1e-77 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HMPBNJCG_00810 | 3.6e-96 | 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 | |
HMPBNJCG_00811 | 3.7e-154 | hlpA | M | Belongs to the NlpA lipoprotein family | ||
HMPBNJCG_00812 | 6.8e-101 | pncA | Q | isochorismatase | ||
HMPBNJCG_00813 | 1.2e-140 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
HMPBNJCG_00814 | 3.7e-240 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
HMPBNJCG_00815 | 2.4e-75 | XK27_03180 | T | universal stress protein | ||
HMPBNJCG_00818 | 2e-157 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
HMPBNJCG_00819 | 2e-239 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
HMPBNJCG_00820 | 2.4e-144 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
HMPBNJCG_00821 | 0.0 | yjcE | P | NhaP-type Na H and K H antiporters | ||
HMPBNJCG_00823 | 1.4e-98 | ytqB | 2.1.1.176 | J | (SAM)-dependent | |
HMPBNJCG_00824 | 1.3e-184 | yhcC | S | radical SAM protein | ||
HMPBNJCG_00825 | 2.2e-196 | ylbL | T | Belongs to the peptidase S16 family | ||
HMPBNJCG_00826 | 2.7e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HMPBNJCG_00827 | 5.1e-93 | rsmD | 2.1.1.171 | L | Methyltransferase | |
HMPBNJCG_00828 | 1.9e-172 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HMPBNJCG_00829 | 1.5e-09 | S | Protein of unknown function (DUF4059) | |||
HMPBNJCG_00830 | 6.5e-131 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
HMPBNJCG_00831 | 4.7e-163 | yxeN | P | ABC transporter (Permease | ||
HMPBNJCG_00832 | 1.5e-152 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
HMPBNJCG_00834 | 3.1e-206 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HMPBNJCG_00835 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
HMPBNJCG_00836 | 1.8e-147 | cah | 4.2.1.1 | P | carbonic anhydrase | |
HMPBNJCG_00837 | 2.1e-85 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
HMPBNJCG_00838 | 1e-44 | hsdS_1 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
HMPBNJCG_00839 | 2.9e-87 | D | nuclear chromosome segregation | |||
HMPBNJCG_00840 | 1.5e-127 | ybbM | S | transport system, permease component | ||
HMPBNJCG_00841 | 1.2e-117 | ybbL | S | abc transporter atp-binding protein | ||
HMPBNJCG_00842 | 4.5e-185 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
HMPBNJCG_00843 | 4.6e-140 | cppA | E | CppA N-terminal | ||
HMPBNJCG_00844 | 5e-44 | V | CAAX protease self-immunity | |||
HMPBNJCG_00845 | 2.3e-164 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HMPBNJCG_00846 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
HMPBNJCG_00849 | 3e-47 | spiA | K | sequence-specific DNA binding | ||
HMPBNJCG_00850 | 2.9e-28 | blpT | ||||
HMPBNJCG_00851 | 6.7e-98 | blpT | ||||
HMPBNJCG_00856 | 4.3e-25 | S | Bacteriocin class II with double-glycine leader peptide | |||
HMPBNJCG_00859 | 8.9e-133 | agrA | KT | phosphorelay signal transduction system | ||
HMPBNJCG_00860 | 3e-235 | blpH | 2.7.13.3 | T | protein histidine kinase activity | |
HMPBNJCG_00862 | 7.3e-237 | mesE | M | Transport protein ComB | ||
HMPBNJCG_00863 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
HMPBNJCG_00864 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
HMPBNJCG_00865 | 0.0 | mdlA | V | abc transporter atp-binding protein | ||
HMPBNJCG_00867 | 1.7e-93 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
HMPBNJCG_00868 | 7.9e-224 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
HMPBNJCG_00869 | 2.3e-72 | yutD | J | protein conserved in bacteria | ||
HMPBNJCG_00870 | 4.3e-269 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
HMPBNJCG_00872 | 7.2e-221 | 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 | |
HMPBNJCG_00873 | 6.3e-185 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HMPBNJCG_00874 | 0.0 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
HMPBNJCG_00875 | 8.1e-46 | ftsL | D | cell division protein FtsL | ||
HMPBNJCG_00876 | 3.9e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HMPBNJCG_00877 | 3e-128 | |||||
HMPBNJCG_00878 | 9.7e-32 | yhaI | J | Protein of unknown function (DUF805) | ||
HMPBNJCG_00879 | 1.3e-08 | D | nuclear chromosome segregation | |||
HMPBNJCG_00880 | 2e-225 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
HMPBNJCG_00881 | 5.7e-141 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HMPBNJCG_00882 | 2.2e-285 | XK27_00765 | ||||
HMPBNJCG_00883 | 8.1e-134 | ecsA_2 | V | abc transporter atp-binding protein | ||
HMPBNJCG_00884 | 5.2e-125 | S | Protein of unknown function (DUF554) | |||
HMPBNJCG_00885 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HMPBNJCG_00886 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination | |
HMPBNJCG_00887 | 9.8e-57 | liaI | S | membrane | ||
HMPBNJCG_00888 | 7e-10 | XK27_02470 | K | LytTr DNA-binding domain protein | ||
HMPBNJCG_00889 | 1.8e-65 | KT | response to antibiotic | |||
HMPBNJCG_00890 | 5.2e-81 | yebC | M | Membrane | ||
HMPBNJCG_00891 | 2.9e-18 | yebC | M | Membrane | ||
HMPBNJCG_00892 | 4.3e-261 | XK27_03190 | 5.2.1.8 | S | hydrolases of the HAD superfamily | |
HMPBNJCG_00893 | 8.5e-173 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
HMPBNJCG_00894 | 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) | |
HMPBNJCG_00895 | 1.9e-182 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HMPBNJCG_00896 | 4.1e-62 | 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 | |
HMPBNJCG_00897 | 1.1e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HMPBNJCG_00898 | 3.8e-198 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HMPBNJCG_00899 | 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 | ||
HMPBNJCG_00901 | 3e-189 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HMPBNJCG_00902 | 4.1e-172 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
HMPBNJCG_00903 | 0.0 | scrA | 2.7.1.211 | G | pts system | |
HMPBNJCG_00904 | 4.1e-291 | scrB | 3.2.1.26 | GH32 | G | invertase |
HMPBNJCG_00905 | 7.5e-180 | scrR | K | Transcriptional | ||
HMPBNJCG_00906 | 2.1e-73 | 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 | ||
HMPBNJCG_00907 | 3.4e-62 | yqhY | S | protein conserved in bacteria | ||
HMPBNJCG_00908 | 1.2e-97 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
HMPBNJCG_00909 | 3.7e-84 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HMPBNJCG_00910 | 5e-193 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
HMPBNJCG_00912 | 8e-44 | V | 'abc transporter, ATP-binding protein | |||
HMPBNJCG_00913 | 1e-58 | V | 'abc transporter, ATP-binding protein | |||
HMPBNJCG_00916 | 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 | ||
HMPBNJCG_00917 | 2e-169 | corA | P | COG0598 Mg2 and Co2 transporters | ||
HMPBNJCG_00918 | 3.1e-124 | XK27_01040 | S | Pfam PF06570 | ||
HMPBNJCG_00920 | 9.7e-36 | 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 | ||
HMPBNJCG_00921 | 2.7e-91 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
HMPBNJCG_00922 | 3.9e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HMPBNJCG_00923 | 2.8e-31 | XK27_05745 | ||||
HMPBNJCG_00924 | 2.5e-230 | mutY | L | A G-specific adenine glycosylase | ||
HMPBNJCG_00929 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HMPBNJCG_00930 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
HMPBNJCG_00931 | 1e-93 | cvpA | S | toxin biosynthetic process | ||
HMPBNJCG_00932 | 2.3e-13 | 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 | ||
HMPBNJCG_00933 | 4.7e-160 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HMPBNJCG_00934 | 1.3e-113 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HMPBNJCG_00935 | 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 | |
HMPBNJCG_00936 | 2e-47 | azlD | E | branched-chain amino acid | ||
HMPBNJCG_00937 | 1.8e-114 | azlC | E | AzlC protein | ||
HMPBNJCG_00938 | 1.9e-186 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
HMPBNJCG_00939 | 4.8e-73 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
HMPBNJCG_00940 | 5.6e-121 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
HMPBNJCG_00941 | 2.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
HMPBNJCG_00942 | 0.0 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HMPBNJCG_00943 | 2.7e-40 | pscB | M | CHAP domain protein | ||
HMPBNJCG_00944 | 1.5e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HMPBNJCG_00945 | 8.5e-63 | glnR | K | Transcriptional regulator | ||
HMPBNJCG_00946 | 1.3e-87 | S | Fusaric acid resistance protein-like | |||
HMPBNJCG_00947 | 2e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HMPBNJCG_00948 | 3.2e-42 | L | Transposase | |||
HMPBNJCG_00949 | 1.9e-46 | L | transposase activity | |||
HMPBNJCG_00950 | 1.4e-189 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HMPBNJCG_00951 | 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 | ||
HMPBNJCG_00952 | 6.7e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
HMPBNJCG_00953 | 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 | ||
HMPBNJCG_00954 | 1.1e-142 | purR | 2.4.2.7 | F | operon repressor | |
HMPBNJCG_00955 | 3.6e-179 | cbf | S | 3'-5' exoribonuclease yhaM | ||
HMPBNJCG_00956 | 6.9e-173 | rmuC | S | RmuC domain protein | ||
HMPBNJCG_00957 | 3.1e-118 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HMPBNJCG_00958 | 8.6e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
HMPBNJCG_00959 | 6.4e-162 | rsgA | 3.1.3.100 | G | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
HMPBNJCG_00961 | 8.9e-156 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
HMPBNJCG_00962 | 1.1e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
HMPBNJCG_00963 | 1.6e-143 | tatD | L | Hydrolase, tatd | ||
HMPBNJCG_00964 | 7.2e-74 | yccU | S | CoA-binding protein | ||
HMPBNJCG_00965 | 4.8e-51 | trxA | O | Belongs to the thioredoxin family | ||
HMPBNJCG_00966 | 1.9e-141 | S | Macro domain protein | |||
HMPBNJCG_00967 | 2e-09 | L | thioesterase | |||
HMPBNJCG_00968 | 2.2e-54 | bta | 1.8.1.8 | CO | cell redox homeostasis | |
HMPBNJCG_00971 | 1.7e-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) | |
HMPBNJCG_00972 | 2.7e-62 | L | Transposase | |||
HMPBNJCG_00973 | 1e-13 | rpmH | J | Ribosomal protein L34 | ||
HMPBNJCG_00974 | 2e-186 | jag | S | RNA-binding protein | ||
HMPBNJCG_00975 | 7.5e-141 | 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 | ||
HMPBNJCG_00976 | 5.9e-55 | 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 | |
HMPBNJCG_00977 | 4.1e-264 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
HMPBNJCG_00978 | 2e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HMPBNJCG_00979 | 2.1e-282 | 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) | |
HMPBNJCG_00980 | 6.7e-81 | amiA | E | transmembrane transport | ||
HMPBNJCG_00981 | 4.2e-74 | amiA | E | transmembrane transport | ||
HMPBNJCG_00982 | 4.8e-120 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HMPBNJCG_00983 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HMPBNJCG_00984 | 3.5e-50 | S | Protein of unknown function (DUF3397) | |||
HMPBNJCG_00985 | 2e-88 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HMPBNJCG_00986 | 7.3e-59 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
HMPBNJCG_00987 | 6.2e-12 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
HMPBNJCG_00988 | 1.4e-226 | 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 | ||
HMPBNJCG_00989 | 1.1e-80 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
HMPBNJCG_00990 | 1.8e-19 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
HMPBNJCG_00991 | 4.3e-77 | XK27_09620 | S | reductase | ||
HMPBNJCG_00992 | 2.1e-32 | XK27_09615 | S | FMN reductase (NADPH) activity | ||
HMPBNJCG_00993 | 1.2e-131 | XK27_09615 | S | PAS domain | ||
HMPBNJCG_00994 | 1.9e-07 | fnt | P | Formate nitrite transporter | ||
HMPBNJCG_00995 | 6.4e-54 | fnt | P | Formate nitrite transporter | ||
HMPBNJCG_00996 | 7.2e-64 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
HMPBNJCG_00997 | 2.8e-185 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HMPBNJCG_00998 | 1.8e-170 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HMPBNJCG_00999 | 2.8e-117 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
HMPBNJCG_01000 | 3.5e-94 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HMPBNJCG_01001 | 3e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HMPBNJCG_01002 | 8.1e-59 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HMPBNJCG_01003 | 1.6e-21 | S | glycolate biosynthetic process | |||
HMPBNJCG_01004 | 1.5e-64 | S | phosphatase activity | |||
HMPBNJCG_01005 | 2e-157 | rrmA | 2.1.1.187 | Q | methyltransferase | |
HMPBNJCG_01008 | 2.7e-91 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HMPBNJCG_01009 | 1.9e-65 | ssb_2 | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
HMPBNJCG_01010 | 2.4e-36 | yeeD | O | sulfur carrier activity | ||
HMPBNJCG_01011 | 1.8e-187 | yeeE | S | Sulphur transport | ||
HMPBNJCG_01012 | 7.9e-114 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HMPBNJCG_01013 | 4.2e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
HMPBNJCG_01014 | 4.1e-09 | S | Domain of unknown function (DUF4651) | |||
HMPBNJCG_01015 | 2e-205 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
HMPBNJCG_01016 | 3.9e-131 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HMPBNJCG_01017 | 1.8e-111 | S | CAAX amino terminal protease family protein | |||
HMPBNJCG_01019 | 5e-67 | V | CAAX protease self-immunity | |||
HMPBNJCG_01020 | 1.4e-33 | V | CAAX protease self-immunity | |||
HMPBNJCG_01021 | 8.8e-27 | lanR | K | sequence-specific DNA binding | ||
HMPBNJCG_01022 | 2.9e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HMPBNJCG_01023 | 7.7e-177 | ytxK | 2.1.1.72 | L | DNA methylase | |
HMPBNJCG_01024 | 6.8e-13 | comGF | U | Putative Competence protein ComGF | ||
HMPBNJCG_01025 | 4e-72 | comGF | U | Competence protein ComGF | ||
HMPBNJCG_01026 | 1.4e-15 | NU | Type II secretory pathway pseudopilin | |||
HMPBNJCG_01027 | 1.8e-57 | cglD | NU | Competence protein | ||
HMPBNJCG_01028 | 8.5e-43 | comGC | U | Required for transformation and DNA binding | ||
HMPBNJCG_01029 | 9.2e-153 | cglB | NU | type II secretion system | ||
HMPBNJCG_01030 | 1.9e-175 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
HMPBNJCG_01031 | 2.9e-68 | S | cog cog4699 | |||
HMPBNJCG_01032 | 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 | |
HMPBNJCG_01033 | 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 | |
HMPBNJCG_01034 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HMPBNJCG_01035 | 1.2e-238 | 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) | |
HMPBNJCG_01036 | 1.6e-196 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
HMPBNJCG_01037 | 7.7e-77 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
HMPBNJCG_01038 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
HMPBNJCG_01039 | 8.8e-281 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HMPBNJCG_01040 | 8.4e-09 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HMPBNJCG_01041 | 1.7e-304 | yloV | S | kinase related to dihydroxyacetone kinase | ||
HMPBNJCG_01042 | 1.8e-57 | asp | S | cog cog1302 | ||
HMPBNJCG_01043 | 3.2e-226 | norN | V | Mate efflux family protein | ||
HMPBNJCG_01044 | 1.9e-278 | thrC | 4.2.3.1 | E | Threonine synthase | |
HMPBNJCG_01045 | 1.9e-65 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HMPBNJCG_01046 | 1.2e-35 | adhE | 1.1.1.1, 1.2.1.10 | C | hydroxyacid-oxoacid transhydrogenase activity | |
HMPBNJCG_01047 | 3.5e-76 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HMPBNJCG_01048 | 1.3e-135 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HMPBNJCG_01049 | 1.4e-63 | adhE | 1.1.1.1, 1.2.1.10 | C | Dehydrogenase | |
HMPBNJCG_01050 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HMPBNJCG_01051 | 2.8e-38 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
HMPBNJCG_01052 | 1.2e-69 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
HMPBNJCG_01053 | 1.3e-65 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
HMPBNJCG_01054 | 1.4e-54 | treB | 2.7.1.201 | G | PTS System | |
HMPBNJCG_01055 | 5.8e-21 | treR | K | DNA-binding transcription factor activity | ||
HMPBNJCG_01056 | 1.2e-85 | treR | K | trehalose operon | ||
HMPBNJCG_01057 | 3.3e-95 | ywlG | S | Belongs to the UPF0340 family | ||
HMPBNJCG_01060 | 2e-35 | L | PFAM Integrase, catalytic core | |||
HMPBNJCG_01061 | 2e-94 | L | PFAM Integrase, catalytic core | |||
HMPBNJCG_01062 | 3.3e-46 | K | Putative DNA-binding domain | |||
HMPBNJCG_01063 | 2.5e-13 | 2.3.1.82 | M | Acetyltransferase GNAT Family | ||
HMPBNJCG_01064 | 1.2e-126 | gltT | C | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
HMPBNJCG_01065 | 6.4e-136 | HJ | the current gene model (or a revised gene model) may contain a frame shift | |||
HMPBNJCG_01070 | 1e-39 | |||||
HMPBNJCG_01071 | 6.5e-31 | |||||
HMPBNJCG_01072 | 5e-31 | S | Hypothetical protein (DUF2513) | |||
HMPBNJCG_01073 | 7.7e-13 | |||||
HMPBNJCG_01075 | 3.7e-216 | S | MvaI/BcnI restriction endonuclease family | |||
HMPBNJCG_01077 | 2.2e-282 | dcm | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
HMPBNJCG_01078 | 9e-164 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
HMPBNJCG_01080 | 6.7e-110 | 6.3.2.2 | H | ergothioneine biosynthetic process | ||
HMPBNJCG_01081 | 1.5e-65 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
HMPBNJCG_01082 | 3.2e-12 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
HMPBNJCG_01083 | 3.3e-09 | L | PFAM Integrase, catalytic core | |||
HMPBNJCG_01084 | 1.8e-111 | L | PFAM Integrase, catalytic core | |||
HMPBNJCG_01085 | 3.3e-62 | rplQ | J | ribosomal protein l17 | ||
HMPBNJCG_01086 | 4.8e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HMPBNJCG_01087 | 9.6e-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 | ||
HMPBNJCG_01088 | 4e-57 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
HMPBNJCG_01089 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HMPBNJCG_01090 | 2.7e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
HMPBNJCG_01091 | 9.2e-121 | 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 | |
HMPBNJCG_01092 | 2.1e-230 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
HMPBNJCG_01093 | 4.4e-58 | rplO | J | binds to the 23S rRNA | ||
HMPBNJCG_01094 | 2.5e-23 | rpmD | J | ribosomal protein l30 | ||
HMPBNJCG_01095 | 1.7e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HMPBNJCG_01096 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
HMPBNJCG_01097 | 2.3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
HMPBNJCG_01098 | 1.2e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
HMPBNJCG_01099 | 1.5e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HMPBNJCG_01100 | 1.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
HMPBNJCG_01101 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HMPBNJCG_01102 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HMPBNJCG_01103 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HMPBNJCG_01104 | 2.7e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HMPBNJCG_01105 | 7.2e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HMPBNJCG_01106 | 2.1e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HMPBNJCG_01107 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
HMPBNJCG_01108 | 4.9e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HMPBNJCG_01109 | 8.8e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
HMPBNJCG_01110 | 2.4e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HMPBNJCG_01111 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HMPBNJCG_01112 | 1.1e-110 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
HMPBNJCG_01113 | 1.3e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HMPBNJCG_01114 | 7.8e-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 | |
HMPBNJCG_01115 | 0.0 | XK27_09800 | I | Acyltransferase | ||
HMPBNJCG_01116 | 1.7e-35 | XK27_09805 | S | MORN repeat protein | ||
HMPBNJCG_01117 | 1e-80 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HMPBNJCG_01118 | 4.1e-250 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
HMPBNJCG_01119 | 1.5e-89 | adk | 2.7.4.3 | F | topology modulation protein | |
HMPBNJCG_01120 | 8.6e-127 | Z012_04635 | K | sequence-specific DNA binding | ||
HMPBNJCG_01122 | 6.3e-16 | C | Radical SAM | |||
HMPBNJCG_01123 | 3.4e-191 | C | Radical SAM | |||
HMPBNJCG_01124 | 3.9e-287 | V | ABC transporter transmembrane region | |||
HMPBNJCG_01125 | 2.5e-89 | K | sequence-specific DNA binding | |||
HMPBNJCG_01126 | 1e-36 | L | Replication initiation factor | |||
HMPBNJCG_01127 | 1.4e-107 | L | Replication initiation factor | |||
HMPBNJCG_01128 | 1.9e-18 | S | Domain of unknown function (DUF3173) | |||
HMPBNJCG_01129 | 3.5e-216 | int | L | Belongs to the 'phage' integrase family | ||
HMPBNJCG_01131 | 5.2e-237 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
HMPBNJCG_01132 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
HMPBNJCG_01133 | 2.8e-44 | yrzL | S | Belongs to the UPF0297 family | ||
HMPBNJCG_01134 | 1.2e-70 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HMPBNJCG_01135 | 4.2e-44 | yrzB | S | Belongs to the UPF0473 family | ||
HMPBNJCG_01136 | 6.6e-301 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
HMPBNJCG_01137 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HMPBNJCG_01138 | 7.5e-14 | |||||
HMPBNJCG_01139 | 2.6e-91 | XK27_10930 | K | acetyltransferase | ||
HMPBNJCG_01140 | 3.7e-116 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
HMPBNJCG_01141 | 2.3e-41 | yaaA | S | Belongs to the UPF0246 family | ||
HMPBNJCG_01142 | 1.2e-50 | yaaA | S | Belongs to the UPF0246 family | ||
HMPBNJCG_01143 | 9.9e-169 | XK27_01785 | S | cog cog1284 | ||
HMPBNJCG_01144 | 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) | |
HMPBNJCG_01146 | 1.6e-241 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
HMPBNJCG_01147 | 5.7e-52 | metE | 2.1.1.14 | E | Methionine synthase | |
HMPBNJCG_01148 | 7.6e-64 | metE | 2.1.1.14 | E | Methionine synthase | |
HMPBNJCG_01149 | 9.2e-36 | metE | 2.1.1.14 | E | Methionine synthase | |
HMPBNJCG_01150 | 2e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HMPBNJCG_01151 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HMPBNJCG_01153 | 3.1e-20 | yegS | 2.7.1.107 | I | lipid kinase activity | |
HMPBNJCG_01154 | 2.7e-95 | S | Hydrophobic domain protein | |||
HMPBNJCG_01156 | 3.7e-27 | S | Membrane | |||
HMPBNJCG_01157 | 3.1e-101 | |||||
HMPBNJCG_01158 | 1.8e-23 | S | Small integral membrane protein | |||
HMPBNJCG_01159 | 1.1e-71 | M | Protein conserved in bacteria | |||
HMPBNJCG_01160 | 4.9e-12 | K | CsbD-like | |||
HMPBNJCG_01161 | 3.5e-97 | nudL | L | hydrolase | ||
HMPBNJCG_01162 | 3.4e-13 | nudL | L | hydrolase | ||
HMPBNJCG_01163 | 4e-19 | K | negative regulation of transcription, DNA-templated | |||
HMPBNJCG_01164 | 1.7e-23 | K | negative regulation of transcription, DNA-templated | |||
HMPBNJCG_01166 | 1.8e-19 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
HMPBNJCG_01167 | 1.8e-88 | S | Putative adhesin | |||
HMPBNJCG_01168 | 3.9e-161 | XK27_06930 | V | domain protein | ||
HMPBNJCG_01169 | 6.4e-96 | XK27_06935 | K | transcriptional regulator | ||
HMPBNJCG_01170 | 4.8e-55 | ypaA | M | Membrane | ||
HMPBNJCG_01171 | 2.7e-08 | |||||
HMPBNJCG_01172 | 9.8e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
HMPBNJCG_01173 | 8.2e-48 | veg | S | Biofilm formation stimulator VEG | ||
HMPBNJCG_01174 | 1.5e-245 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HMPBNJCG_01175 | 3.9e-70 | rplI | J | binds to the 23S rRNA | ||
HMPBNJCG_01176 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HMPBNJCG_01177 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
HMPBNJCG_01178 | 1.5e-77 | F | NUDIX domain | |||
HMPBNJCG_01179 | 8.6e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
HMPBNJCG_01180 | 0.0 | S | Bacterial membrane protein, YfhO | |||
HMPBNJCG_01181 | 1.5e-88 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
HMPBNJCG_01182 | 5.3e-85 | lytE | M | LysM domain protein | ||
HMPBNJCG_01183 | 2e-138 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HMPBNJCG_01184 | 5.2e-153 | 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 | |
HMPBNJCG_01185 | 1.5e-152 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HMPBNJCG_01186 | 3.1e-90 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HMPBNJCG_01187 | 6.3e-138 | ymfM | S | sequence-specific DNA binding | ||
HMPBNJCG_01188 | 3.1e-242 | ymfH | S | Peptidase M16 | ||
HMPBNJCG_01189 | 4.8e-235 | ymfF | S | Peptidase M16 | ||
HMPBNJCG_01190 | 2.4e-44 | yaaA | S | S4 domain protein YaaA | ||
HMPBNJCG_01191 | 5.9e-205 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
HMPBNJCG_01192 | 4.3e-275 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
HMPBNJCG_01193 | 6.3e-193 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
HMPBNJCG_01194 | 4.2e-153 | yvjA | S | membrane | ||
HMPBNJCG_01195 | 6.7e-306 | ybiT | S | abc transporter atp-binding protein | ||
HMPBNJCG_01196 | 0.0 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
HMPBNJCG_01200 | 6.2e-120 | yoaK | S | Psort location CytoplasmicMembrane, score | ||
HMPBNJCG_01201 | 1.1e-86 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HMPBNJCG_01202 | 2.6e-193 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
HMPBNJCG_01203 | 8.5e-134 | parB | K | Belongs to the ParB family | ||
HMPBNJCG_01204 | 1.3e-257 | 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 | ||
HMPBNJCG_01205 | 6.3e-202 | 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 | |
HMPBNJCG_01206 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
HMPBNJCG_01207 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HMPBNJCG_01208 | 1.4e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HMPBNJCG_01209 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
HMPBNJCG_01210 | 1.7e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
HMPBNJCG_01211 | 2.7e-61 | divIC | D | Septum formation initiator | ||
HMPBNJCG_01213 | 8.7e-240 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
HMPBNJCG_01214 | 5e-240 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
HMPBNJCG_01215 | 3.4e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HMPBNJCG_01216 | 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 | ||
HMPBNJCG_01217 | 1.3e-137 | L | Transposase | |||
HMPBNJCG_01218 | 6.4e-33 | cpsJ | S | Glycosyltransferase like family 2 | ||
HMPBNJCG_01219 | 3e-15 | |||||
HMPBNJCG_01220 | 1.1e-71 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
HMPBNJCG_01221 | 1.9e-41 | pssE | S | Glycosyltransferase family 28 C-terminal domain | ||
HMPBNJCG_01222 | 1.4e-72 | cpsF | M | Oligosaccharide biosynthesis protein Alg14 like | ||
HMPBNJCG_01223 | 1.2e-70 | rfbP | 2.7.8.6 | M | Bacterial sugar transferase | |
HMPBNJCG_01224 | 3.3e-37 | L | transposase activity | |||
HMPBNJCG_01225 | 4e-60 | L | COG2801 Transposase and inactivated derivatives | |||
HMPBNJCG_01226 | 2.4e-30 | tra981A | L | Integrase core domain | ||
HMPBNJCG_01227 | 8.1e-52 | tnp | L | DDE domain | ||
HMPBNJCG_01228 | 1.4e-235 | cps1C | S | Polysaccharide biosynthesis protein | ||
HMPBNJCG_01233 | 2.6e-10 | |||||
HMPBNJCG_01236 | 1.9e-07 | |||||
HMPBNJCG_01241 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HMPBNJCG_01242 | 8.6e-237 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
HMPBNJCG_01243 | 5.5e-36 | XK27_02060 | S | Transglycosylase associated protein | ||
HMPBNJCG_01244 | 1.7e-54 | badR | K | DNA-binding transcription factor activity | ||
HMPBNJCG_01245 | 1e-96 | S | reductase | |||
HMPBNJCG_01246 | 2.3e-31 | L | Integrase core domain protein | |||
HMPBNJCG_01247 | 6.2e-36 | L | transposition | |||
HMPBNJCG_01248 | 1.9e-22 | yocD | 3.4.17.13 | V | carboxypeptidase activity | |
HMPBNJCG_01249 | 3.8e-87 | yocD | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
HMPBNJCG_01252 | 1.3e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HMPBNJCG_01253 | 1.7e-182 | 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 | ||
HMPBNJCG_01254 | 1.1e-83 | S | Putative small multi-drug export protein | |||
HMPBNJCG_01255 | 6.2e-76 | ctsR | K | Belongs to the CtsR family | ||
HMPBNJCG_01256 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
HMPBNJCG_01257 | 3.2e-151 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HMPBNJCG_01258 | 1.8e-32 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HMPBNJCG_01259 | 1.4e-231 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HMPBNJCG_01260 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
HMPBNJCG_01261 | 6.9e-144 | S | SseB protein N-terminal domain | |||
HMPBNJCG_01262 | 1.1e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
HMPBNJCG_01263 | 1.7e-259 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HMPBNJCG_01264 | 4.2e-68 | 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) | ||
HMPBNJCG_01267 | 5.7e-135 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HMPBNJCG_01268 | 3.5e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
HMPBNJCG_01269 | 3.4e-155 | degV | S | DegV family | ||
HMPBNJCG_01270 | 1.8e-31 | K | helix-turn-helix | |||
HMPBNJCG_01271 | 6.1e-182 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HMPBNJCG_01272 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HMPBNJCG_01273 | 9.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HMPBNJCG_01274 | 1.5e-35 | K | sequence-specific DNA binding | |||
HMPBNJCG_01276 | 0.0 | S | Lantibiotic dehydratase, C terminus | |||
HMPBNJCG_01277 | 2.4e-231 | spaC2 | V | Lanthionine synthetase C family protein | ||
HMPBNJCG_01278 | 4.3e-183 | EGP | Major facilitator Superfamily | |||
HMPBNJCG_01279 | 5.9e-24 | 3.6.4.12 | ||||
HMPBNJCG_01280 | 5.9e-91 | 3.6.4.12 | K | Divergent AAA domain protein | ||
HMPBNJCG_01281 | 7.4e-225 | int | L | Belongs to the 'phage' integrase family | ||
HMPBNJCG_01282 | 1.8e-38 | S | Helix-turn-helix domain | |||
HMPBNJCG_01283 | 4.9e-173 | |||||
HMPBNJCG_01285 | 3.4e-75 | isp2 | S | pathogenesis | ||
HMPBNJCG_01286 | 5.7e-91 | tnp | L | Transposase | ||
HMPBNJCG_01287 | 3.3e-225 | capA | M | Bacterial capsule synthesis protein | ||
HMPBNJCG_01288 | 3.6e-39 | gcvR | T | UPF0237 protein | ||
HMPBNJCG_01289 | 1.9e-242 | XK27_08635 | S | UPF0210 protein | ||
HMPBNJCG_01290 | 2.2e-38 | ais | G | alpha-ribazole phosphatase activity | ||
HMPBNJCG_01291 | 1.6e-143 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
HMPBNJCG_01292 | 1.3e-102 | acmA | 3.2.1.17 | NU | amidase activity | |
HMPBNJCG_01293 | 5.3e-198 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HMPBNJCG_01294 | 1.3e-71 | 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 | ||
HMPBNJCG_01295 | 9.8e-298 | dnaK | O | Heat shock 70 kDa protein | ||
HMPBNJCG_01296 | 4.2e-190 | 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 | ||
HMPBNJCG_01297 | 2.5e-138 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HMPBNJCG_01298 | 6.2e-137 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
HMPBNJCG_01299 | 1.7e-60 | hmpT | S | membrane | ||
HMPBNJCG_01302 | 1.2e-165 | L | integrase core domain | |||
HMPBNJCG_01303 | 2e-52 | L | Transposase | |||
HMPBNJCG_01304 | 1.6e-249 | L | Transposase | |||
HMPBNJCG_01305 | 9.9e-19 | S | Domain of unknown function (DUF4649) | |||
HMPBNJCG_01306 | 1.8e-56 | amd | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
HMPBNJCG_01307 | 1.5e-233 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
HMPBNJCG_01308 | 6.5e-87 | |||||
HMPBNJCG_01309 | 1.6e-77 | sigH | K | DNA-templated transcription, initiation | ||
HMPBNJCG_01310 | 3.5e-149 | ykuT | M | mechanosensitive ion channel | ||
HMPBNJCG_01311 | 7.1e-218 | 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 | ||
HMPBNJCG_01312 | 4.8e-73 | 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 | ||
HMPBNJCG_01313 | 7.6e-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 | |
HMPBNJCG_01314 | 1.1e-83 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
HMPBNJCG_01315 | 3.7e-81 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
HMPBNJCG_01316 | 2e-177 | prmA | J | Ribosomal protein L11 methyltransferase | ||
HMPBNJCG_01317 | 4.4e-135 | 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 | |
HMPBNJCG_01318 | 1.4e-42 | F | nucleotide catabolic process | |||
HMPBNJCG_01319 | 5.4e-139 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
HMPBNJCG_01320 | 7.7e-140 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
HMPBNJCG_01321 | 2.3e-51 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
HMPBNJCG_01322 | 1.8e-83 | nrdI | F | Belongs to the NrdI family | ||
HMPBNJCG_01323 | 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 | |
HMPBNJCG_01324 | 2.3e-75 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
HMPBNJCG_01325 | 1.4e-09 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
HMPBNJCG_01326 | 2e-27 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
HMPBNJCG_01327 | 2.1e-58 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
HMPBNJCG_01328 | 3.9e-46 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
HMPBNJCG_01329 | 1.7e-237 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
HMPBNJCG_01330 | 3.3e-112 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
HMPBNJCG_01331 | 5.3e-113 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
HMPBNJCG_01332 | 6.5e-202 | yhjX | P | Major Facilitator | ||
HMPBNJCG_01333 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HMPBNJCG_01334 | 5e-94 | V | VanZ like family | |||
HMPBNJCG_01335 | 1e-123 | glnQ | E | abc transporter atp-binding protein | ||
HMPBNJCG_01336 | 5.8e-275 | glnP | P | ABC transporter | ||
HMPBNJCG_01337 | 9.1e-153 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
HMPBNJCG_01338 | 1.3e-134 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HMPBNJCG_01339 | 1.9e-185 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
HMPBNJCG_01340 | 9.5e-144 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
HMPBNJCG_01341 | 1.4e-234 | sufD | O | assembly protein SufD | ||
HMPBNJCG_01342 | 7.7e-238 | 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 | |
HMPBNJCG_01343 | 2.5e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HMPBNJCG_01344 | 2.2e-273 | sufB | O | assembly protein SufB | ||
HMPBNJCG_01345 | 7e-10 | oppA | E | ABC transporter substrate-binding protein | ||
HMPBNJCG_01346 | 2e-138 | oppA | E | ABC transporter substrate-binding protein | ||
HMPBNJCG_01347 | 4.2e-27 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HMPBNJCG_01348 | 6.6e-11 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HMPBNJCG_01349 | 1.7e-33 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HMPBNJCG_01350 | 1.4e-38 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HMPBNJCG_01351 | 3e-27 | oppD | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_01352 | 2.5e-32 | oppD | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_01353 | 1.2e-62 | oppD | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_01354 | 3.1e-43 | oppD | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_01355 | 7.5e-62 | oppF | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_01356 | 4.4e-62 | oppF | P | Belongs to the ABC transporter superfamily | ||
HMPBNJCG_01357 | 6.4e-23 | |||||
HMPBNJCG_01358 | 2.1e-157 | 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 | ||
HMPBNJCG_01359 | 7.4e-183 | 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 | ||
HMPBNJCG_01360 | 1.9e-223 | EGP | Major facilitator Superfamily | |||
HMPBNJCG_01361 | 3.1e-72 | adcR | K | transcriptional | ||
HMPBNJCG_01362 | 2.2e-136 | adcC | P | ABC transporter, ATP-binding protein | ||
HMPBNJCG_01363 | 1.6e-127 | adcB | P | ABC transporter (Permease | ||
HMPBNJCG_01364 | 1.4e-162 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
HMPBNJCG_01365 | 5.6e-65 | ptsG | 2.7.1.199, 2.7.1.208 | G | pts system | |
HMPBNJCG_01366 | 2.1e-150 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | pts system | |
HMPBNJCG_01367 | 1.4e-105 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |
HMPBNJCG_01368 | 6.8e-158 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
HMPBNJCG_01369 | 2.8e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HMPBNJCG_01370 | 1.9e-127 | yeeN | K | transcriptional regulatory protein | ||
HMPBNJCG_01371 | 9.8e-50 | yajC | U | protein transport | ||
HMPBNJCG_01372 | 1.1e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HMPBNJCG_01373 | 2.2e-145 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
HMPBNJCG_01374 | 1.4e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HMPBNJCG_01375 | 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 | |
HMPBNJCG_01376 | 0.0 | WQ51_06230 | S | ABC transporter substrate binding protein | ||
HMPBNJCG_01377 | 5.2e-142 | cmpC | S | abc transporter atp-binding protein | ||
HMPBNJCG_01378 | 1.3e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HMPBNJCG_01379 | 4.1e-287 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HMPBNJCG_01380 | 4.4e-37 | L | Transposase | |||
HMPBNJCG_01381 | 6.4e-18 | L | transposase activity | |||
HMPBNJCG_01384 | 4.7e-43 | |||||
HMPBNJCG_01385 | 6.8e-56 | S | TM2 domain | |||
HMPBNJCG_01386 | 1.2e-165 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HMPBNJCG_01387 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HMPBNJCG_01388 | 5.7e-25 | secE | U | Belongs to the SecE SEC61-gamma family | ||
HMPBNJCG_01389 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HMPBNJCG_01390 | 4.6e-85 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
HMPBNJCG_01391 | 6e-55 | cof | Q | phosphatase activity | ||
HMPBNJCG_01392 | 6.2e-35 | cof | Q | phosphatase activity | ||
HMPBNJCG_01393 | 1.6e-137 | glcR | K | transcriptional regulator (DeoR family) | ||
HMPBNJCG_01394 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HMPBNJCG_01395 | 3.8e-40 | K | transcriptional | |||
HMPBNJCG_01397 | 2.6e-76 | S | thiolester hydrolase activity | |||
HMPBNJCG_01398 | 1e-139 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
HMPBNJCG_01399 | 5.7e-280 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HMPBNJCG_01400 | 2.1e-151 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
HMPBNJCG_01401 | 1.9e-77 | yhaI | L | Membrane | ||
HMPBNJCG_01402 | 5.1e-259 | pepC | 3.4.22.40 | E | aminopeptidase | |
HMPBNJCG_01403 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HMPBNJCG_01404 | 2.5e-109 | 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 | ||
HMPBNJCG_01405 | 3.1e-95 | ypsA | S | Belongs to the UPF0398 family | ||
HMPBNJCG_01406 | 2.5e-50 | 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 | ||
HMPBNJCG_01407 | 1.5e-222 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HMPBNJCG_01408 | 2.5e-296 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
HMPBNJCG_01409 | 0.0 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
HMPBNJCG_01410 | 2.5e-23 | |||||
HMPBNJCG_01411 | 2.6e-255 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HMPBNJCG_01412 | 7.3e-80 | XK27_09675 | K | -acetyltransferase | ||
HMPBNJCG_01413 | 0.0 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
HMPBNJCG_01414 | 1.6e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
HMPBNJCG_01415 | 5.2e-59 | L | Integrase core domain protein | |||
HMPBNJCG_01416 | 2.9e-165 | 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 | ||
HMPBNJCG_01417 | 7e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HMPBNJCG_01418 | 6.4e-131 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HMPBNJCG_01419 | 6.1e-93 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
HMPBNJCG_01420 | 8.8e-98 | ybhL | S | Belongs to the BI1 family | ||
HMPBNJCG_01423 | 9.6e-244 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HMPBNJCG_01424 | 3.7e-91 | K | transcriptional regulator | |||
HMPBNJCG_01425 | 7.6e-36 | yneF | S | UPF0154 protein | ||
HMPBNJCG_01426 | 3.8e-148 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HMPBNJCG_01427 | 7.1e-186 | 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 | |
HMPBNJCG_01428 | 3.5e-99 | XK27_09740 | S | Phosphoesterase | ||
HMPBNJCG_01429 | 7.8e-85 | ykuL | S | CBS domain | ||
HMPBNJCG_01430 | 4.5e-135 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
HMPBNJCG_01431 | 3.8e-120 | 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 | ||
HMPBNJCG_01432 | 3e-99 | 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 | ||
HMPBNJCG_01433 | 6.1e-140 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HMPBNJCG_01434 | 1.2e-39 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
HMPBNJCG_01435 | 1.2e-258 | trkH | P | Cation transport protein | ||
HMPBNJCG_01436 | 1.5e-247 | trkA | P | Potassium transporter peripheral membrane component | ||
HMPBNJCG_01437 | 7.9e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HMPBNJCG_01438 | 3.2e-90 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
HMPBNJCG_01439 | 4.8e-114 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
HMPBNJCG_01440 | 5.6e-161 | K | sequence-specific DNA binding | |||
HMPBNJCG_01441 | 1.2e-32 | V | protein secretion by the type I secretion system | |||
HMPBNJCG_01442 | 7.4e-36 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
HMPBNJCG_01443 | 4.3e-57 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
HMPBNJCG_01444 | 1.6e-25 | V | protein secretion by the type I secretion system | |||
HMPBNJCG_01445 | 1.8e-27 | comA | V | protein secretion by the type I secretion system | ||
HMPBNJCG_01446 | 3.4e-68 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
HMPBNJCG_01447 | 3.7e-51 | yhaI | L | Membrane | ||
HMPBNJCG_01448 | 6.7e-36 | S | Domain of unknown function (DUF4173) | |||
HMPBNJCG_01449 | 9.2e-132 | S | Domain of unknown function (DUF4173) | |||
HMPBNJCG_01450 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
HMPBNJCG_01451 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
HMPBNJCG_01452 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
HMPBNJCG_01453 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
HMPBNJCG_01454 | 6.6e-78 | ureE | O | enzyme active site formation | ||
HMPBNJCG_01455 | 5.3e-130 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
HMPBNJCG_01456 | 9.5e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
HMPBNJCG_01457 | 1.3e-159 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
HMPBNJCG_01458 | 2.7e-177 | cbiM | P | PDGLE domain | ||
HMPBNJCG_01459 | 1.1e-136 | P | cobalt transport protein | |||
HMPBNJCG_01460 | 1.6e-131 | cbiO | P | ABC transporter | ||
HMPBNJCG_01461 | 5.3e-153 | ET | amino acid transport | |||
HMPBNJCG_01462 | 4.1e-78 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
HMPBNJCG_01463 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
HMPBNJCG_01464 | 0.0 | 3.3.1.1, 3.6.1.55, 3.6.1.67 | F | NUDIX domain | ||
HMPBNJCG_01465 | 3.8e-205 | EGP | Transmembrane secretion effector | |||
HMPBNJCG_01466 | 1.8e-153 | ET | amino acid transport | |||
HMPBNJCG_01467 | 7.1e-164 | metQ | M | Belongs to the NlpA lipoprotein family | ||
HMPBNJCG_01468 | 4.9e-87 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
HMPBNJCG_01469 | 1.2e-61 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase activity | |
HMPBNJCG_01470 | 1.4e-62 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase activity | |
HMPBNJCG_01471 | 1.2e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HMPBNJCG_01472 | 5.2e-98 | metI | P | ABC transporter (Permease | ||
HMPBNJCG_01473 | 3.9e-210 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
HMPBNJCG_01474 | 5.5e-158 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
HMPBNJCG_01475 | 8e-94 | S | UPF0397 protein | |||
HMPBNJCG_01476 | 0.0 | ykoD | P | abc transporter atp-binding protein | ||
HMPBNJCG_01477 | 1.2e-146 | cbiQ | P | cobalt transport | ||
HMPBNJCG_01478 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
HMPBNJCG_01479 | 1.4e-11 | ulaG | S | L-ascorbate 6-phosphate lactonase | ||
HMPBNJCG_01480 | 1.4e-121 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
HMPBNJCG_01481 | 1.2e-244 | P | COG0168 Trk-type K transport systems, membrane components | |||
HMPBNJCG_01482 | 1.1e-130 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
HMPBNJCG_01483 | 2.4e-90 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
HMPBNJCG_01484 | 3e-122 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HMPBNJCG_01485 | 2.8e-282 | T | PhoQ Sensor | |||
HMPBNJCG_01486 | 4.7e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HMPBNJCG_01487 | 6.5e-218 | dnaB | L | Replication initiation and membrane attachment | ||
HMPBNJCG_01488 | 4.4e-166 | dnaI | L | Primosomal protein DnaI | ||
HMPBNJCG_01489 | 2.6e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HMPBNJCG_01491 | 1.2e-34 | |||||
HMPBNJCG_01492 | 3e-27 | L | Integrase core domain protein | |||
HMPBNJCG_01493 | 3.4e-50 | L | transposition | |||
HMPBNJCG_01494 | 5.7e-23 | L | Transposase | |||
HMPBNJCG_01495 | 7.8e-28 | L | transposase activity | |||
HMPBNJCG_01496 | 8.6e-232 | 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) | |
HMPBNJCG_01497 | 4.2e-62 | manO | S | protein conserved in bacteria | ||
HMPBNJCG_01498 | 6.2e-168 | manN | G | PTS system mannose fructose sorbose family IID component | ||
HMPBNJCG_01499 | 2.3e-116 | manM | G | pts system | ||
HMPBNJCG_01500 | 1.1e-181 | manL | 2.7.1.191 | G | pts system | |
HMPBNJCG_01501 | 1.5e-140 | XK27_00940 | 1.2.1.70, 3.5.1.9 | S | Metal-dependent hydrolase | |
HMPBNJCG_01502 | 1e-153 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
HMPBNJCG_01503 | 1.9e-248 | pbuO | S | permease | ||
HMPBNJCG_01504 | 1.4e-77 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
HMPBNJCG_01505 | 2.4e-92 | XK27_05885 | 2.3.1.82 | M | Acetyltransferase GNAT Family | |
HMPBNJCG_01506 | 2.5e-220 | brpA | K | Transcriptional | ||
HMPBNJCG_01507 | 3.9e-81 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
HMPBNJCG_01508 | 3.1e-212 | nusA | K | Participates in both transcription termination and antitermination | ||
HMPBNJCG_01509 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
HMPBNJCG_01510 | 1.4e-41 | ylxQ | J | ribosomal protein | ||
HMPBNJCG_01511 | 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 | ||
HMPBNJCG_01512 | 1.7e-57 | 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 | ||
HMPBNJCG_01513 | 2e-22 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
HMPBNJCG_01514 | 1.5e-25 | yvdD | 3.2.2.10 | S | cytokinin biosynthetic process | |
HMPBNJCG_01515 | 3.6e-48 | femA | 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
HMPBNJCG_01516 | 6.2e-85 | femA | 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
HMPBNJCG_01517 | 3.2e-49 | femA | 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
HMPBNJCG_01518 | 4.9e-276 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HMPBNJCG_01519 | 4.5e-283 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
HMPBNJCG_01520 | 3.3e-96 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
HMPBNJCG_01521 | 4.7e-202 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
HMPBNJCG_01522 | 1e-223 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
HMPBNJCG_01525 | 4.4e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HMPBNJCG_01526 | 2.9e-105 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
HMPBNJCG_01527 | 1.2e-74 | ylbF | S | Belongs to the UPF0342 family | ||
HMPBNJCG_01528 | 7.1e-46 | ylbG | S | UPF0298 protein | ||
HMPBNJCG_01529 | 1.3e-210 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
HMPBNJCG_01530 | 1.9e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
HMPBNJCG_01531 | 1.4e-138 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
HMPBNJCG_01532 | 9.6e-138 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
HMPBNJCG_01533 | 4.8e-123 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
HMPBNJCG_01534 | 6.8e-69 | acuB | S | IMP dehydrogenase activity | ||
HMPBNJCG_01535 | 8.9e-41 | acuB | S | IMP dehydrogenase activity | ||
HMPBNJCG_01536 | 3.7e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HMPBNJCG_01537 | 1.1e-110 | yvyE | 3.4.13.9 | S | YigZ family | |
HMPBNJCG_01538 | 4.5e-252 | comFA | L | Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
HMPBNJCG_01539 | 1.7e-122 | comFC | S | Competence protein | ||
HMPBNJCG_01540 | 2.1e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HMPBNJCG_01547 | 2.1e-166 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
HMPBNJCG_01548 | 6.4e-108 | S | Domain of unknown function (DUF1803) | |||
HMPBNJCG_01549 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
HMPBNJCG_01550 | 1.2e-130 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HMPBNJCG_01551 | 6.7e-259 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HMPBNJCG_01552 | 8e-193 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
HMPBNJCG_01553 | 2.6e-255 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HMPBNJCG_01554 | 6.8e-75 | S | Haloacid dehalogenase-like hydrolase | |||
HMPBNJCG_01555 | 2.4e-139 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
HMPBNJCG_01556 | 4e-72 | marR | K | Transcriptional regulator, MarR family | ||
HMPBNJCG_01557 | 2.3e-173 | 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 | |
HMPBNJCG_01558 | 3.3e-30 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HMPBNJCG_01559 | 5.8e-172 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
HMPBNJCG_01560 | 8.5e-165 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
HMPBNJCG_01561 | 1.6e-126 | IQ | reductase | |||
HMPBNJCG_01562 | 2.6e-233 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
HMPBNJCG_01563 | 7.7e-56 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
HMPBNJCG_01564 | 1.5e-71 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
HMPBNJCG_01565 | 1.7e-257 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
HMPBNJCG_01566 | 1.6e-160 | 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 | |
HMPBNJCG_01567 | 1.1e-138 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
HMPBNJCG_01568 | 4.7e-90 | 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) | |
HMPBNJCG_01569 | 1.1e-65 | tnp | L | Transposase | ||
HMPBNJCG_01570 | 2.3e-214 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
HMPBNJCG_01571 | 9.8e-176 | gadC | E | Psort location CytoplasmicMembrane, score 10.00 | ||
HMPBNJCG_01572 | 4.7e-27 | L | Transposase and inactivated derivatives, TnpA family | |||
HMPBNJCG_01573 | 3.4e-126 | tnp | L | Transposase | ||
HMPBNJCG_01575 | 8e-277 | S | Protein of unknown function (DUF3114) | |||
HMPBNJCG_01576 | 1.7e-51 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
HMPBNJCG_01577 | 7.7e-198 | V | (ABC) transporter | |||
HMPBNJCG_01578 | 1.4e-74 | C | Arylsulfatase regulator (Fe-S oxidoreductase) | |||
HMPBNJCG_01579 | 6.4e-85 | C | Arylsulfatase regulator (Fe-S oxidoreductase) | |||
HMPBNJCG_01580 | 1.1e-113 | K | sequence-specific DNA binding | |||
HMPBNJCG_01581 | 8.4e-155 | L | COG2801 Transposase and inactivated derivatives | |||
HMPBNJCG_01582 | 6.6e-38 | L | transposase activity | |||
HMPBNJCG_01583 | 1.3e-205 | rny | D | Endoribonuclease that initiates mRNA decay | ||
HMPBNJCG_01584 | 1.8e-84 | L | Transposase | |||
HMPBNJCG_01585 | 5.5e-122 | fruR | K | transcriptional | ||
HMPBNJCG_01586 | 3.8e-165 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
HMPBNJCG_01587 | 0.0 | fruA | 2.7.1.202 | G | phosphotransferase system | |
HMPBNJCG_01588 | 2.7e-260 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HMPBNJCG_01589 | 2.6e-241 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HMPBNJCG_01591 | 6.1e-213 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
HMPBNJCG_01592 | 6.5e-229 | 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 | |
HMPBNJCG_01593 | 4.9e-295 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
HMPBNJCG_01594 | 7.2e-258 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
HMPBNJCG_01595 | 6.4e-29 | 2.3.1.128 | K | acetyltransferase | ||
HMPBNJCG_01596 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HMPBNJCG_01597 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HMPBNJCG_01598 | 7.7e-134 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
HMPBNJCG_01599 | 2.6e-64 | WQ51_03320 | S | cog cog4835 | ||
HMPBNJCG_01600 | 9.8e-91 | XK27_08360 | S | EDD domain protein, DegV family | ||
HMPBNJCG_01601 | 3e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HMPBNJCG_01602 | 9.6e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
HMPBNJCG_01603 | 0.0 | yfmR | S | abc transporter atp-binding protein | ||
HMPBNJCG_01604 | 1.6e-24 | U | response to pH | |||
HMPBNJCG_01605 | 1.1e-141 | 3.6.1.13, 3.6.1.55 | F | AdP-ribose pyrophosphatase | ||
HMPBNJCG_01606 | 1.7e-212 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | adenylyltransferase | |
HMPBNJCG_01607 | 1.8e-256 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
HMPBNJCG_01608 | 1e-69 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HMPBNJCG_01609 | 9.4e-77 | K | DNA-binding transcription factor activity | |||
HMPBNJCG_01610 | 0.0 | lmrA1 | V | abc transporter atp-binding protein | ||
HMPBNJCG_01611 | 0.0 | lmrA2 | V | abc transporter atp-binding protein | ||
HMPBNJCG_01612 | 5.4e-45 | K | Acetyltransferase (GNAT) family | |||
HMPBNJCG_01613 | 3.2e-78 | sptS | 2.7.13.3 | T | Histidine kinase | |
HMPBNJCG_01614 | 4.9e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HMPBNJCG_01615 | 1.3e-91 | 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 | ||
HMPBNJCG_01616 | 5.3e-161 | cvfB | S | Protein conserved in bacteria | ||
HMPBNJCG_01617 | 7.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
HMPBNJCG_01618 | 6.7e-124 | usp | 3.5.1.104, 3.5.1.28 | CBM50 | S | pathogenesis |
HMPBNJCG_01619 | 2.3e-61 | rlpA | M | LysM domain protein | ||
HMPBNJCG_01620 | 2.3e-190 | phoH | T | phosphate starvation-inducible protein PhoH | ||
HMPBNJCG_01624 | 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 | |
HMPBNJCG_01625 | 1.8e-164 | K | transcriptional regulator (lysR family) | |||
HMPBNJCG_01626 | 1.4e-186 | coiA | 3.6.4.12 | S | Competence protein | |
HMPBNJCG_01627 | 0.0 | pepF | E | oligoendopeptidase F | ||
HMPBNJCG_01628 | 5.4e-127 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
HMPBNJCG_01629 | 1.3e-167 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
HMPBNJCG_01630 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
HMPBNJCG_01631 | 7.9e-24 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
HMPBNJCG_01632 | 6.9e-179 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
HMPBNJCG_01633 | 3.9e-120 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
HMPBNJCG_01634 | 4.9e-145 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
HMPBNJCG_01635 | 1.7e-226 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
HMPBNJCG_01636 | 1.4e-189 | 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 | |
HMPBNJCG_01637 | 1.5e-222 | 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 | |
HMPBNJCG_01638 | 7.9e-129 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
HMPBNJCG_01639 | 1.6e-210 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
HMPBNJCG_01640 | 2.2e-130 | yxkH | G | deacetylase | ||
HMPBNJCG_01641 | 2.3e-237 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HMPBNJCG_01642 | 2.8e-154 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HMPBNJCG_01643 | 5.5e-153 | rarD | S | Transporter | ||
HMPBNJCG_01644 | 2.2e-15 | T | peptidase | |||
HMPBNJCG_01645 | 8.9e-14 | coiA | 3.6.4.12 | S | Competence protein | |
HMPBNJCG_01646 | 4.1e-112 | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | |||
HMPBNJCG_01647 | 1.9e-46 | 2.3.1.128, 5.2.1.8 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
HMPBNJCG_01648 | 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 | |
HMPBNJCG_01649 | 3.2e-16 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
HMPBNJCG_01650 | 4.3e-124 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HMPBNJCG_01651 | 3.3e-78 | atpF | C | ATP synthase F(0) sector subunit b | ||
HMPBNJCG_01652 | 9.3e-87 | 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 | ||
HMPBNJCG_01653 | 3.8e-279 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
HMPBNJCG_01654 | 7.4e-158 | 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 | ||
HMPBNJCG_01655 | 2.7e-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 | |
HMPBNJCG_01656 | 5.2e-67 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HMPBNJCG_01657 | 2.8e-230 | ftsW | D | Belongs to the SEDS family | ||
HMPBNJCG_01658 | 9.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HMPBNJCG_01659 | 1.4e-136 | 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) | |
HMPBNJCG_01660 | 2.8e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HMPBNJCG_01661 | 1.9e-161 | holB | 2.7.7.7 | L | dna polymerase iii | |
HMPBNJCG_01662 | 2.1e-135 | yaaT | S | stage 0 sporulation protein | ||
HMPBNJCG_01663 | 1.1e-34 | yabA | L | Involved in initiation control of chromosome replication | ||
HMPBNJCG_01664 | 3.9e-159 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HMPBNJCG_01665 | 7.5e-233 | amt | P | Ammonium Transporter | ||
HMPBNJCG_01666 | 1.1e-53 | glnB | K | Belongs to the P(II) protein family | ||
HMPBNJCG_01667 | 4.9e-106 | mur1 | NU | mannosyl-glycoprotein | ||
HMPBNJCG_01668 | 1.7e-148 | XK27_04800 | S | Sucrose-6F-phosphate phosphohydrolase | ||
HMPBNJCG_01669 | 2.9e-68 | nptA | P | sodium-dependent phosphate transmembrane transporter activity | ||
HMPBNJCG_01670 | 2.1e-221 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
HMPBNJCG_01671 | 1.8e-53 | |||||
HMPBNJCG_01672 | 7.5e-26 | |||||
HMPBNJCG_01673 | 1.5e-59 | |||||
HMPBNJCG_01674 | 6.1e-63 | S | membrane | |||
HMPBNJCG_01675 | 4.8e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HMPBNJCG_01676 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
HMPBNJCG_01677 | 4.5e-39 | ynzC | S | UPF0291 protein | ||
HMPBNJCG_01678 | 1.8e-254 | cycA | E | permease | ||
HMPBNJCG_01679 | 1.1e-09 | uvrX | 2.7.7.7 | L | ImpB mucB samB family | |
HMPBNJCG_01680 | 2.8e-24 | 2.7.1.208, 2.7.1.211 | G | protein-N(PI)-phosphohistidine-sugar phosphotransferase activity | ||
HMPBNJCG_01681 | 5.8e-71 | pts33BCA | G | pts system | ||
HMPBNJCG_01682 | 9e-96 | pts33BCA | G | pts system | ||
HMPBNJCG_01683 | 9.7e-77 | 2.7.1.199, 2.7.1.211 | G | PTS glucose transporter subunit IIA | ||
HMPBNJCG_01684 | 3.2e-141 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
HMPBNJCG_01689 | 1.4e-167 | fhuR | K | transcriptional regulator (lysR family) | ||
HMPBNJCG_01690 | 1.5e-77 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HMPBNJCG_01691 | 4.5e-163 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HMPBNJCG_01692 | 3.7e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HMPBNJCG_01693 | 4.9e-227 | pyrP | F | uracil Permease | ||
HMPBNJCG_01694 | 1e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HMPBNJCG_01695 | 1.1e-211 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
HMPBNJCG_01696 | 0.0 | carB | 6.3.5.5 | F | carbamoyl-phosphate synthetase ammonia chain | |
HMPBNJCG_01697 | 2.2e-134 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
HMPBNJCG_01698 | 4e-37 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
HMPBNJCG_01699 | 1.6e-33 | V | permease protein | |||
HMPBNJCG_01700 | 1e-09 | V | permease protein | |||
HMPBNJCG_01701 | 8.8e-21 | V | permease protein | |||
HMPBNJCG_01702 | 1.7e-07 | V | efflux transmembrane transporter activity | |||
HMPBNJCG_01703 | 1.1e-24 | ytrF | V | efflux transmembrane transporter activity | ||
HMPBNJCG_01704 | 5.6e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HMPBNJCG_01705 | 3.9e-52 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HMPBNJCG_01707 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
HMPBNJCG_01708 | 0.0 | lmrA | V | abc transporter atp-binding protein | ||
HMPBNJCG_01709 | 4.6e-199 | 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) | |
HMPBNJCG_01710 | 5.8e-121 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
HMPBNJCG_01711 | 6.3e-214 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
HMPBNJCG_01712 | 2.5e-132 | rr02 | KT | response regulator | ||
HMPBNJCG_01713 | 3.5e-202 | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | ||
HMPBNJCG_01714 | 4.8e-168 | V | ABC transporter | |||
HMPBNJCG_01715 | 5.4e-122 | sagI | S | ABC-2 type transporter | ||
HMPBNJCG_01716 | 4.5e-196 | yceA | S | Belongs to the UPF0176 family | ||
HMPBNJCG_01717 | 8e-28 | XK27_00085 | K | Transcriptional | ||
HMPBNJCG_01718 | 1.7e-23 | |||||
HMPBNJCG_01719 | 1.2e-143 | deoD_1 | 2.4.2.3 | F | Phosphorylase superfamily | |
HMPBNJCG_01720 | 2.8e-112 | S | VIT family | |||
HMPBNJCG_01721 | 7.4e-132 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HMPBNJCG_01722 | 2.4e-217 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
HMPBNJCG_01723 | 3.4e-17 | ald | 1.4.1.1 | E | alanine dehydrogenase activity | |
HMPBNJCG_01724 | 2e-47 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
HMPBNJCG_01725 | 5.7e-247 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HMPBNJCG_01726 | 8.8e-104 | GBS0088 | J | protein conserved in bacteria | ||
HMPBNJCG_01727 | 2.5e-142 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
HMPBNJCG_01728 | 1.5e-172 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
HMPBNJCG_01729 | 1.6e-177 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases N terminal domain | |
HMPBNJCG_01730 | 7.6e-191 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
HMPBNJCG_01731 | 1.5e-253 | 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 | |
HMPBNJCG_01732 | 1e-96 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
HMPBNJCG_01733 | 2.5e-21 | |||||
HMPBNJCG_01734 | 2e-118 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
HMPBNJCG_01736 | 3.5e-07 | U | protein secretion | |||
HMPBNJCG_01737 | 2.5e-51 | U | protein secretion | |||
HMPBNJCG_01738 | 7.4e-08 | M | Pilin isopeptide linkage domain protein | |||
HMPBNJCG_01739 | 7.6e-191 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
HMPBNJCG_01740 | 1.5e-247 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
HMPBNJCG_01741 | 3.5e-49 | XK27_13030 | ||||
HMPBNJCG_01742 | 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) | |
HMPBNJCG_01743 | 8.3e-55 | S | hydrolase activity, acting on ester bonds | |||
HMPBNJCG_01744 | 9.4e-71 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
HMPBNJCG_01745 | 6.8e-164 | S | Protein of unknown function (DUF3114) | |||
HMPBNJCG_01746 | 1.2e-22 | S | Protein of unknown function (DUF3114) | |||
HMPBNJCG_01747 | 1.5e-118 | yqfA | K | protein, Hemolysin III | ||
HMPBNJCG_01748 | 1e-25 | K | hmm pf08876 | |||
HMPBNJCG_01749 | 2.7e-233 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HMPBNJCG_01750 | 1.7e-218 | mvaS | 2.3.3.10 | I | synthase | |
HMPBNJCG_01751 | 2.2e-167 | 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 | |
HMPBNJCG_01752 | 3.4e-91 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
HMPBNJCG_01753 | 9.7e-22 | |||||
HMPBNJCG_01754 | 2e-225 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
HMPBNJCG_01755 | 3e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HMPBNJCG_01756 | 1.5e-250 | mmuP | E | amino acid | ||
HMPBNJCG_01757 | 1.2e-177 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
HMPBNJCG_01758 | 1.4e-29 | S | Domain of unknown function (DUF1912) | |||
HMPBNJCG_01759 | 4.9e-15 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
HMPBNJCG_01760 | 7.1e-102 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
HMPBNJCG_01761 | 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 | |
HMPBNJCG_01762 | 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 | |
HMPBNJCG_01763 | 2.4e-200 | ilvE | 2.6.1.42 | E | Aminotransferase | |
HMPBNJCG_01764 | 4.8e-16 | S | Protein of unknown function (DUF2969) | |||
HMPBNJCG_01767 | 8.4e-205 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
HMPBNJCG_01770 | 1.1e-44 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
HMPBNJCG_01771 | 1.3e-29 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
HMPBNJCG_01772 | 3.7e-70 | M | Pfam SNARE associated Golgi protein | |||
HMPBNJCG_01773 | 3.4e-233 | murN | 2.3.2.10, 2.3.2.16 | V | FemAB family | |
HMPBNJCG_01774 | 1.6e-08 | S | oxidoreductase | |||
HMPBNJCG_01775 | 9.3e-59 | S | oxidoreductase | |||
HMPBNJCG_01776 | 9.7e-66 | S | oxidoreductase | |||
HMPBNJCG_01777 | 3.7e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
HMPBNJCG_01778 | 1.8e-86 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
HMPBNJCG_01779 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
HMPBNJCG_01780 | 1.2e-180 | 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 | |
HMPBNJCG_01781 | 1.3e-34 | ykuJ | S | protein conserved in bacteria | ||
HMPBNJCG_01782 | 7.5e-118 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
HMPBNJCG_01783 | 2.2e-131 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HMPBNJCG_01784 | 3.1e-78 | feoA | P | FeoA domain protein | ||
HMPBNJCG_01785 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HMPBNJCG_01786 | 1.5e-07 | |||||
HMPBNJCG_01787 | 2.4e-104 | 1.1.1.133, 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 | ||
HMPBNJCG_01788 | 2.2e-45 | K | sequence-specific DNA binding | |||
HMPBNJCG_01789 | 1.5e-35 | yugF | I | carboxylic ester hydrolase activity | ||
HMPBNJCG_01790 | 7.5e-23 | I | Alpha/beta hydrolase family | |||
HMPBNJCG_01791 | 3.9e-156 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
HMPBNJCG_01792 | 7.8e-149 | 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 | |
HMPBNJCG_01793 | 0.0 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
HMPBNJCG_01794 | 4.9e-105 | 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 | ||
HMPBNJCG_01795 | 5.8e-64 | licT | K | transcriptional antiterminator | ||
HMPBNJCG_01796 | 6.8e-53 | licT | K | transcriptional antiterminator | ||
HMPBNJCG_01797 | 5.9e-88 | 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 | |
HMPBNJCG_01798 | 1.7e-64 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
HMPBNJCG_01799 | 1.3e-165 | era | M | 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 | ||
HMPBNJCG_01800 | 1.9e-155 | 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 | |
HMPBNJCG_01801 | 1.1e-104 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18 | GH23 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
HMPBNJCG_01802 | 2.5e-220 | mdtG | EGP | Major facilitator Superfamily | ||
HMPBNJCG_01803 | 2e-33 | secG | U | Preprotein translocase subunit SecG | ||
HMPBNJCG_01804 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HMPBNJCG_01805 | 1.1e-80 | smpB | O | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
HMPBNJCG_01806 | 9.6e-277 | 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 | |
HMPBNJCG_01807 | 1.7e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
HMPBNJCG_01808 | 4.2e-211 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
HMPBNJCG_01809 | 4.4e-183 | ccpA | K | Catabolite control protein A | ||
HMPBNJCG_01810 | 2.8e-28 | yyaQ | S | YjbR | ||
HMPBNJCG_01811 | 6.6e-101 | yyaQ | V | Protein conserved in bacteria | ||
HMPBNJCG_01812 | 1.3e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HMPBNJCG_01813 | 1e-78 | yueI | S | Protein of unknown function (DUF1694) | ||
HMPBNJCG_01814 | 9.6e-247 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
HMPBNJCG_01815 | 2e-25 | WQ51_00785 | ||||
HMPBNJCG_01816 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
HMPBNJCG_01817 | 2e-219 | ywbD | 2.1.1.191 | J | Methyltransferase | |
HMPBNJCG_01818 | 8.6e-122 | 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 | |
HMPBNJCG_01819 | 1.7e-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) | |
HMPBNJCG_01820 | 3.5e-202 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
HMPBNJCG_01821 | 4.5e-219 | 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 | |
HMPBNJCG_01822 | 2.2e-207 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
HMPBNJCG_01823 | 3.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
HMPBNJCG_01824 | 3e-173 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HMPBNJCG_01825 | 2.6e-236 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
HMPBNJCG_01826 | 1.7e-87 | 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 | |
HMPBNJCG_01827 | 6.7e-153 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
HMPBNJCG_01828 | 6.4e-252 | msrR | K | Transcriptional regulator | ||
HMPBNJCG_01829 | 2.2e-149 | ydiA | P | C4-dicarboxylate transporter malic acid transport protein | ||
HMPBNJCG_01830 | 2.4e-203 | I | acyl-CoA dehydrogenase | |||
HMPBNJCG_01831 | 4.5e-97 | mip | S | hydroperoxide reductase activity | ||
HMPBNJCG_01832 | 1.7e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HMPBNJCG_01833 | 8.9e-20 | |||||
HMPBNJCG_01834 | 3.2e-46 | |||||
HMPBNJCG_01835 | 1e-31 | K | Cro/C1-type HTH DNA-binding domain | |||
HMPBNJCG_01836 | 7.8e-50 | dam | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
HMPBNJCG_01837 | 9.7e-34 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
HMPBNJCG_01838 | 1.1e-94 | |||||
HMPBNJCG_01839 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
HMPBNJCG_01840 | 4.2e-172 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HMPBNJCG_01841 | 3.1e-53 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HMPBNJCG_01842 | 2.6e-194 | S | CRISPR-associated protein Csn2 subfamily St | |||
HMPBNJCG_01843 | 2.7e-146 | ycgQ | S | TIGR03943 family | ||
HMPBNJCG_01844 | 4.6e-155 | XK27_03015 | S | permease | ||
HMPBNJCG_01846 | 0.0 | yhgF | K | Transcriptional accessory protein | ||
HMPBNJCG_01847 | 9.9e-42 | pspC | KT | PspC domain | ||
HMPBNJCG_01848 | 2e-169 | 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 | ||
HMPBNJCG_01849 | 4e-147 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HMPBNJCG_01851 | 5.5e-69 | ytxH | S | General stress protein | ||
HMPBNJCG_01853 | 2e-177 | yegQ | O | Peptidase U32 | ||
HMPBNJCG_01854 | 3.4e-252 | yegQ | O | Peptidase U32 | ||
HMPBNJCG_01855 | 8.1e-46 | S | CHY zinc finger | |||
HMPBNJCG_01856 | 8.4e-88 | bioY | S | biotin synthase | ||
HMPBNJCG_01858 | 1.1e-33 | XK27_12190 | S | protein conserved in bacteria | ||
HMPBNJCG_01859 | 1.1e-234 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HMPBNJCG_01860 | 4.8e-11 | |||||
HMPBNJCG_01861 | 6e-209 | dcm | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
HMPBNJCG_01862 | 4.1e-225 | mutH | L | DNA mismatch repair enzyme MutH | ||
HMPBNJCG_01863 | 5.2e-29 | S | SIR2-like domain | |||
HMPBNJCG_01864 | 1.2e-33 | S | SIR2-like domain | |||
HMPBNJCG_01865 | 9.2e-286 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HMPBNJCG_01866 | 6.4e-158 | M | LysM domain | |||
HMPBNJCG_01867 | 7.6e-16 | |||||
HMPBNJCG_01868 | 2.3e-175 | S | hydrolase | |||
HMPBNJCG_01869 | 1.9e-115 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase | |
HMPBNJCG_01870 | 7.9e-82 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
HMPBNJCG_01871 | 1.6e-145 | XK27_00880 | 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
HMPBNJCG_01872 | 2.7e-27 | P | Hemerythrin HHE cation binding domain protein | |||
HMPBNJCG_01873 | 2.3e-113 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
HMPBNJCG_01874 | 0.0 | hsdR | 3.1.21.3 | V | Type I restriction enzyme R protein N terminus (HSDR_N) | |
HMPBNJCG_01875 | 3.9e-290 | hsdM | 2.1.1.72 | V | N-6 DNA Methylase | |
HMPBNJCG_01876 | 2.2e-147 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
HMPBNJCG_01878 | 2.5e-44 | |||||
HMPBNJCG_01879 | 3e-38 | |||||
HMPBNJCG_01880 | 2.3e-171 | spd | F | DNA RNA non-specific endonuclease | ||
HMPBNJCG_01881 | 1.5e-92 | lemA | S | LemA family | ||
HMPBNJCG_01882 | 1.8e-135 | htpX | O | Belongs to the peptidase M48B family | ||
HMPBNJCG_01883 | 4.2e-75 | S | Psort location CytoplasmicMembrane, score | |||
HMPBNJCG_01884 | 6.2e-56 | S | Domain of unknown function (DUF4430) | |||
HMPBNJCG_01885 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HMPBNJCG_01886 | 1.2e-183 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HMPBNJCG_01887 | 8.5e-113 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
HMPBNJCG_01888 | 5.4e-161 | L | Transposase | |||
HMPBNJCG_01889 | 3e-50 | L | Transposase | |||
HMPBNJCG_01890 | 2.6e-189 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
HMPBNJCG_01891 | 4.4e-115 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
HMPBNJCG_01892 | 3.5e-91 | dps | P | Belongs to the Dps family | ||
HMPBNJCG_01893 | 1.1e-80 | perR | P | Belongs to the Fur family | ||
HMPBNJCG_01894 | 8.4e-28 | yqgQ | S | protein conserved in bacteria | ||
HMPBNJCG_01895 | 2.2e-179 | glk | 2.7.1.2 | G | Glucokinase | |
HMPBNJCG_01896 | 0.0 | typA | T | GTP-binding protein TypA | ||
HMPBNJCG_01898 | 1.6e-252 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HMPBNJCG_01899 | 1e-201 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
HMPBNJCG_01900 | 1.8e-177 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HMPBNJCG_01901 | 8e-252 | 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 | ||
HMPBNJCG_01902 | 5.4e-237 | 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 | ||
HMPBNJCG_01903 | 2.3e-122 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
HMPBNJCG_01904 | 6.8e-96 | sepF | D | cell septum assembly | ||
HMPBNJCG_01905 | 2.6e-34 | yggT | D | integral membrane protein | ||
HMPBNJCG_01906 | 4.2e-144 | ylmH | T | S4 RNA-binding domain | ||
HMPBNJCG_01907 | 1.8e-135 | divIVA | D | Cell division protein DivIVA | ||
HMPBNJCG_01908 | 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) | |
HMPBNJCG_01909 | 5.5e-30 | |||||
HMPBNJCG_01910 | 8.4e-10 | |||||
HMPBNJCG_01911 | 3.2e-231 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
HMPBNJCG_01912 | 2e-45 | rpmE2 | J | 50S ribosomal protein L31 | ||
HMPBNJCG_01913 | 8.3e-176 | 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 | |
HMPBNJCG_01914 | 1e-184 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
HMPBNJCG_01915 | 8.9e-155 | gst | O | Glutathione S-transferase | ||
HMPBNJCG_01916 | 4.6e-188 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
HMPBNJCG_01917 | 4.5e-111 | tdk | 2.7.1.21 | F | thymidine kinase | |
HMPBNJCG_01918 | 3e-193 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HMPBNJCG_01919 | 1.2e-154 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
HMPBNJCG_01920 | 9.7e-109 | 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 | |
HMPBNJCG_01921 | 1.8e-234 | 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 | |
HMPBNJCG_01922 | 1.2e-177 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
HMPBNJCG_01923 | 8e-100 | pvaA | M | lytic transglycosylase activity | ||
HMPBNJCG_01924 | 0.0 | yfiB1 | V | abc transporter atp-binding protein | ||
HMPBNJCG_01925 | 0.0 | XK27_10035 | V | abc transporter atp-binding protein | ||
HMPBNJCG_01926 | 1.7e-09 | S | D-Ala-teichoic acid biosynthesis protein | |||
HMPBNJCG_01927 | 1.4e-297 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HMPBNJCG_01928 | 3.9e-237 | dltB | M | Membrane protein involved in D-alanine export | ||
HMPBNJCG_01929 | 1.7e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HMPBNJCG_01930 | 3.6e-230 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)