ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HKNIGPJH_00001 | 1.3e-36 | S | AAA domain | |||
HKNIGPJH_00002 | 3.4e-123 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
HKNIGPJH_00003 | 1.3e-45 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00004 | 6.3e-31 | 1.1.1.1 | C | Iron-containing alcohol dehydrogenase | ||
HKNIGPJH_00005 | 3.3e-129 | trpF | 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
HKNIGPJH_00006 | 4.6e-74 | E | ABC transporter, substrate-binding protein, family 5 | |||
HKNIGPJH_00007 | 5.1e-96 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00008 | 4e-13 | S | Domain of unknown function (DUF4143) | |||
HKNIGPJH_00009 | 1.4e-121 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
HKNIGPJH_00010 | 4.4e-55 | 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 | ||
HKNIGPJH_00011 | 2.7e-117 | 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) | |
HKNIGPJH_00012 | 9.6e-62 | 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 | ||
HKNIGPJH_00013 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
HKNIGPJH_00014 | 2.8e-148 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HKNIGPJH_00015 | 2e-34 | |||||
HKNIGPJH_00016 | 1.3e-246 | S | zinc finger | |||
HKNIGPJH_00017 | 4.4e-71 | S | Bacterial PH domain | |||
HKNIGPJH_00018 | 1.5e-76 | |||||
HKNIGPJH_00019 | 8.4e-201 | V | Domain of unknown function (DUF3427) | |||
HKNIGPJH_00020 | 0.0 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00021 | 8.1e-185 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
HKNIGPJH_00022 | 9.1e-197 | 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 | ||
HKNIGPJH_00023 | 2.1e-91 | S | membrane transporter protein | |||
HKNIGPJH_00024 | 2e-61 | srtC | 3.4.22.70 | M | Sortase family | |
HKNIGPJH_00025 | 3.8e-38 | G | ABC transporter substrate-binding protein | |||
HKNIGPJH_00026 | 5e-42 | G | ABC transporter substrate-binding protein | |||
HKNIGPJH_00027 | 1.6e-28 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
HKNIGPJH_00028 | 3.6e-23 | yraN | L | Belongs to the UPF0102 family | ||
HKNIGPJH_00029 | 2e-127 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HKNIGPJH_00031 | 2.5e-153 | clcA_2 | P | Voltage gated chloride channel | ||
HKNIGPJH_00032 | 1.3e-218 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
HKNIGPJH_00033 | 3.5e-120 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
HKNIGPJH_00034 | 0.0 | T | Diguanylate cyclase, GGDEF domain | |||
HKNIGPJH_00035 | 2.3e-187 | lacR | K | Transcriptional regulator, LacI family | ||
HKNIGPJH_00036 | 8.7e-235 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
HKNIGPJH_00037 | 1.2e-149 | 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 | |
HKNIGPJH_00038 | 2e-124 | G | Glycosyl hydrolase family 20, domain 2 | |||
HKNIGPJH_00039 | 9e-107 | S | AAA domain | |||
HKNIGPJH_00040 | 3.1e-19 | |||||
HKNIGPJH_00041 | 4.4e-197 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00042 | 2.3e-31 | T | PhoQ Sensor | |||
HKNIGPJH_00043 | 3.6e-168 | S | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00044 | 1.1e-149 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
HKNIGPJH_00045 | 7.3e-25 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
HKNIGPJH_00046 | 2.8e-70 | |||||
HKNIGPJH_00048 | 7.5e-35 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HKNIGPJH_00049 | 2.5e-35 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
HKNIGPJH_00050 | 1.1e-166 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
HKNIGPJH_00051 | 3.3e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HKNIGPJH_00052 | 1.3e-250 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
HKNIGPJH_00053 | 8.6e-139 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
HKNIGPJH_00054 | 1e-27 | S | granule-associated protein | |||
HKNIGPJH_00055 | 0.0 | ubiB | S | ABC1 family | ||
HKNIGPJH_00056 | 1.1e-47 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00057 | 6e-92 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00058 | 0.0 | murJ | KLT | MviN-like protein | ||
HKNIGPJH_00059 | 4.1e-306 | murJ | KLT | MviN-like protein | ||
HKNIGPJH_00060 | 0.0 | M | Conserved repeat domain | |||
HKNIGPJH_00061 | 1.8e-121 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
HKNIGPJH_00062 | 2e-171 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
HKNIGPJH_00063 | 1.5e-208 | srtA | 3.4.22.70 | M | Sortase family | |
HKNIGPJH_00065 | 3.2e-153 | P | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00066 | 2.9e-133 | S | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00067 | 1.8e-181 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00068 | 3.8e-101 | abf | G | Glycosyl hydrolases family 43 | ||
HKNIGPJH_00069 | 1.1e-292 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00070 | 4.6e-169 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00071 | 8.3e-163 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00072 | 2.1e-183 | G | beta-fructofuranosidase activity | |||
HKNIGPJH_00073 | 8.5e-101 | S | Protein of unknown function, DUF624 | |||
HKNIGPJH_00074 | 2.6e-25 | S | Beta-L-arabinofuranosidase, GH127 | |||
HKNIGPJH_00076 | 3.7e-105 | L | Resolvase, N terminal domain | |||
HKNIGPJH_00077 | 5e-50 | tesB | I | Thioesterase-like superfamily | ||
HKNIGPJH_00078 | 6.2e-94 | S | Protein of unknown function (DUF3180) | |||
HKNIGPJH_00079 | 2.6e-58 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
HKNIGPJH_00080 | 3.9e-142 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
HKNIGPJH_00081 | 3e-102 | carD | K | CarD-like/TRCF domain | ||
HKNIGPJH_00082 | 3.3e-142 | mphA | S | Aminoglycoside phosphotransferase | ||
HKNIGPJH_00083 | 3.6e-32 | S | Protein of unknown function (DUF3107) | |||
HKNIGPJH_00084 | 1.8e-178 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
HKNIGPJH_00085 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
HKNIGPJH_00086 | 8.4e-30 | sdpR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
HKNIGPJH_00087 | 8.8e-139 | S | SdpI/YhfL protein family | |||
HKNIGPJH_00088 | 1.9e-36 | S | Domain of unknown function (DUF4956) | |||
HKNIGPJH_00089 | 4.9e-37 | yliE | T | Putative diguanylate phosphodiesterase | ||
HKNIGPJH_00090 | 1.9e-46 | yliE | T | Putative diguanylate phosphodiesterase | ||
HKNIGPJH_00091 | 1.1e-155 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
HKNIGPJH_00092 | 4.1e-101 | V | ABC transporter, ATP-binding protein | |||
HKNIGPJH_00093 | 9e-17 | K | helix_turn_helix ASNC type | |||
HKNIGPJH_00094 | 2.3e-116 | S | Protein of unknown function (DUF4125) | |||
HKNIGPJH_00095 | 1.1e-16 | 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 | |
HKNIGPJH_00096 | 1.1e-77 | soxR | K | MerR, DNA binding | ||
HKNIGPJH_00097 | 3.4e-17 | yccF | S | Inner membrane component domain | ||
HKNIGPJH_00098 | 5.9e-12 | |||||
HKNIGPJH_00099 | 3e-132 | M | Conserved repeat domain | |||
HKNIGPJH_00100 | 8.9e-101 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
HKNIGPJH_00101 | 4.5e-31 | |||||
HKNIGPJH_00102 | 2.3e-164 | 3.6.3.24 | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
HKNIGPJH_00103 | 2.2e-69 | 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 | ||
HKNIGPJH_00104 | 5.1e-63 | 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 | ||
HKNIGPJH_00105 | 2.3e-88 | cat | P | Cation efflux family | ||
HKNIGPJH_00106 | 8.6e-119 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HKNIGPJH_00107 | 9.8e-15 | G | Major Facilitator Superfamily | |||
HKNIGPJH_00108 | 1.7e-151 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HKNIGPJH_00109 | 2.9e-163 | 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 | |
HKNIGPJH_00110 | 4.4e-144 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
HKNIGPJH_00111 | 3.7e-84 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
HKNIGPJH_00112 | 2.6e-149 | 3.2.1.40 | E | Bacterial alpha-L-rhamnosidase C-terminal domain | ||
HKNIGPJH_00113 | 4.3e-192 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
HKNIGPJH_00114 | 3e-267 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
HKNIGPJH_00115 | 2.2e-251 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
HKNIGPJH_00116 | 2.1e-293 | S | Amidohydrolase family | |||
HKNIGPJH_00117 | 1.3e-78 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
HKNIGPJH_00118 | 2.9e-69 | ykiI | ||||
HKNIGPJH_00119 | 2.2e-31 | ykiI | ||||
HKNIGPJH_00120 | 1.8e-33 | P | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00121 | 2e-39 | U | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00123 | 1.5e-19 | macB_8 | V | MacB-like periplasmic core domain | ||
HKNIGPJH_00124 | 2.1e-157 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
HKNIGPJH_00125 | 6.1e-122 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
HKNIGPJH_00126 | 2.5e-36 | |||||
HKNIGPJH_00127 | 1.2e-67 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
HKNIGPJH_00128 | 1.3e-60 | 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 | ||
HKNIGPJH_00129 | 3.5e-80 | trxA2 | O | Tetratricopeptide repeat | ||
HKNIGPJH_00130 | 8e-96 | cyaA | 4.6.1.1 | S | CYTH | |
HKNIGPJH_00131 | 2.7e-56 | VP1224 | V | Psort location CytoplasmicMembrane, score 9.99 | ||
HKNIGPJH_00133 | 1e-93 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00134 | 3.7e-171 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
HKNIGPJH_00135 | 7e-118 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
HKNIGPJH_00136 | 8.7e-93 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HKNIGPJH_00137 | 2.8e-117 | GK | ROK family | |||
HKNIGPJH_00138 | 2.4e-189 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00139 | 1.7e-120 | ftsK | D | FtsK SpoIIIE family protein | ||
HKNIGPJH_00140 | 3.5e-52 | 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 | |
HKNIGPJH_00141 | 1.8e-56 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
HKNIGPJH_00142 | 4.1e-242 | T | Diguanylate cyclase (GGDEF) domain protein | |||
HKNIGPJH_00143 | 1.4e-126 | L | Protein of unknown function (DUF1524) | |||
HKNIGPJH_00144 | 9.3e-166 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
HKNIGPJH_00145 | 8.1e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HKNIGPJH_00146 | 8.9e-198 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00147 | 1.2e-70 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00148 | 1.4e-142 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HKNIGPJH_00149 | 1.8e-99 | 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 | |
HKNIGPJH_00150 | 5.7e-77 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
HKNIGPJH_00151 | 5.5e-29 | |||||
HKNIGPJH_00152 | 2.1e-08 | relB | L | RelB antitoxin | ||
HKNIGPJH_00153 | 1.3e-18 | 3.4.17.13 | E | Rard protein | ||
HKNIGPJH_00154 | 8e-100 | mmuP | E | amino acid | ||
HKNIGPJH_00155 | 2.1e-45 | mmuP | E | amino acid | ||
HKNIGPJH_00156 | 5.2e-167 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
HKNIGPJH_00157 | 1.1e-95 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
HKNIGPJH_00158 | 1.2e-61 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
HKNIGPJH_00159 | 7.6e-63 | S | domain protein | |||
HKNIGPJH_00160 | 9.2e-47 | 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 | |
HKNIGPJH_00161 | 8.8e-41 | V | ABC transporter, ATP-binding protein | |||
HKNIGPJH_00162 | 0.0 | MV | MacB-like periplasmic core domain | |||
HKNIGPJH_00163 | 1.9e-130 | K | helix_turn_helix, Lux Regulon | |||
HKNIGPJH_00164 | 0.0 | tcsS2 | T | Histidine kinase | ||
HKNIGPJH_00165 | 1.7e-125 | 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) | |
HKNIGPJH_00166 | 1.1e-106 | S | Phosphatidylethanolamine-binding protein | |||
HKNIGPJH_00167 | 0.0 | pepD | E | Peptidase family C69 | ||
HKNIGPJH_00168 | 9.1e-289 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
HKNIGPJH_00169 | 6.7e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
HKNIGPJH_00170 | 2.4e-95 | S | GtrA-like protein | |||
HKNIGPJH_00171 | 9.9e-100 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00172 | 1.4e-50 | pknL | 2.7.11.1 | KLT | PASTA | |
HKNIGPJH_00173 | 6.5e-58 | T | Forkhead associated domain | |||
HKNIGPJH_00174 | 2.1e-35 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
HKNIGPJH_00175 | 3.9e-78 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HKNIGPJH_00176 | 3.3e-233 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
HKNIGPJH_00178 | 1.2e-32 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
HKNIGPJH_00179 | 2.9e-129 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HKNIGPJH_00180 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HKNIGPJH_00181 | 3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HKNIGPJH_00182 | 5.9e-143 | QT | PucR C-terminal helix-turn-helix domain | |||
HKNIGPJH_00183 | 3.8e-116 | |||||
HKNIGPJH_00184 | 2e-52 | |||||
HKNIGPJH_00185 | 1.9e-138 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
HKNIGPJH_00186 | 1.2e-86 | 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 | ||
HKNIGPJH_00187 | 1.7e-13 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HKNIGPJH_00188 | 1.3e-129 | cydD | V | ABC transporter transmembrane region | ||
HKNIGPJH_00189 | 9e-127 | dedA | S | SNARE associated Golgi protein | ||
HKNIGPJH_00190 | 1.1e-101 | 1.1.1.65 | C | Aldo/keto reductase family | ||
HKNIGPJH_00191 | 3.2e-09 | S | Protein of unknown function (DUF805) | |||
HKNIGPJH_00192 | 2.9e-97 | |||||
HKNIGPJH_00193 | 4.9e-100 | L | Tetratricopeptide repeat | |||
HKNIGPJH_00194 | 2.1e-25 | V | ABC transporter, ATP-binding protein | |||
HKNIGPJH_00195 | 3.5e-103 | rpsA | J | Ribosomal protein S1 | ||
HKNIGPJH_00196 | 6.2e-160 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
HKNIGPJH_00197 | 5.2e-96 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HKNIGPJH_00198 | 1.2e-65 | |||||
HKNIGPJH_00199 | 4.5e-13 | I | acetylesterase activity | |||
HKNIGPJH_00200 | 7.3e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HKNIGPJH_00201 | 2.2e-116 | aspB | E | Aminotransferase class-V | ||
HKNIGPJH_00202 | 3.4e-126 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
HKNIGPJH_00203 | 1.9e-113 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
HKNIGPJH_00204 | 3.7e-139 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
HKNIGPJH_00205 | 9.2e-86 | XK27_10430 | S | NAD(P)H-binding | ||
HKNIGPJH_00206 | 6.5e-36 | Z012_06715 | V | FtsX-like permease family | ||
HKNIGPJH_00208 | 8e-220 | macB_2 | V | ABC transporter permease | ||
HKNIGPJH_00209 | 4.2e-231 | S | Predicted membrane protein (DUF2318) | |||
HKNIGPJH_00210 | 4.1e-92 | tpd | P | Fe2+ transport protein | ||
HKNIGPJH_00211 | 5.8e-295 | efeU_1 | P | Iron permease FTR1 family | ||
HKNIGPJH_00212 | 1.9e-40 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
HKNIGPJH_00213 | 2.6e-121 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00215 | 7e-60 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
HKNIGPJH_00216 | 2.6e-13 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
HKNIGPJH_00217 | 1.6e-43 | pntAA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
HKNIGPJH_00218 | 4.9e-131 | 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 | |
HKNIGPJH_00219 | 2.7e-38 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
HKNIGPJH_00220 | 8e-57 | G | Fic/DOC family | |||
HKNIGPJH_00221 | 1.4e-25 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
HKNIGPJH_00222 | 3.6e-48 | pcrA | 3.6.4.12 | L | DNA helicase | |
HKNIGPJH_00223 | 2.6e-71 | divIC | D | Septum formation initiator | ||
HKNIGPJH_00224 | 1e-31 | 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 | |
HKNIGPJH_00225 | 9e-121 | U | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00226 | 7.9e-120 | 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 | ||
HKNIGPJH_00227 | 3.6e-174 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
HKNIGPJH_00228 | 6.3e-63 | T | Forkhead associated domain | |||
HKNIGPJH_00229 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
HKNIGPJH_00230 | 4.8e-36 | |||||
HKNIGPJH_00231 | 1.1e-92 | flgA | NO | SAF | ||
HKNIGPJH_00232 | 6.1e-30 | fmdB | S | Putative regulatory protein | ||
HKNIGPJH_00233 | 2e-99 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
HKNIGPJH_00234 | 7.1e-46 | argE | E | Peptidase dimerisation domain | ||
HKNIGPJH_00235 | 5.2e-24 | rodA | D | Belongs to the SEDS family | ||
HKNIGPJH_00236 | 4e-34 | rodA | D | Belongs to the SEDS family | ||
HKNIGPJH_00237 | 6.8e-242 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
HKNIGPJH_00238 | 9.6e-73 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
HKNIGPJH_00239 | 1.2e-131 | fhaA | T | Protein of unknown function (DUF2662) | ||
HKNIGPJH_00240 | 4.5e-65 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
HKNIGPJH_00241 | 5.6e-143 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
HKNIGPJH_00242 | 2.2e-50 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
HKNIGPJH_00243 | 2.5e-269 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00244 | 1.7e-162 | P | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00245 | 6.5e-148 | P | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00246 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
HKNIGPJH_00247 | 6.8e-90 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
HKNIGPJH_00248 | 2.3e-229 | yhjX | EGP | Major facilitator Superfamily | ||
HKNIGPJH_00249 | 3.3e-43 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
HKNIGPJH_00250 | 9.5e-35 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HKNIGPJH_00251 | 3.4e-242 | vex3 | V | ABC transporter permease | ||
HKNIGPJH_00252 | 1.8e-157 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
HKNIGPJH_00253 | 9.3e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00254 | 3.1e-167 | P | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00255 | 4e-07 | P | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00256 | 1.1e-242 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00257 | 4.7e-93 | K | Periplasmic binding protein domain | |||
HKNIGPJH_00258 | 3.1e-289 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
HKNIGPJH_00259 | 1.7e-159 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
HKNIGPJH_00260 | 1.4e-24 | pup | S | Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation | ||
HKNIGPJH_00261 | 1.7e-279 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
HKNIGPJH_00262 | 9.7e-141 | C | FMN binding | |||
HKNIGPJH_00263 | 1.8e-57 | |||||
HKNIGPJH_00264 | 1.4e-41 | hup | L | Belongs to the bacterial histone-like protein family | ||
HKNIGPJH_00265 | 2.9e-136 | G | Phosphoglycerate mutase family | |||
HKNIGPJH_00266 | 6.6e-259 | amyE | G | Bacterial extracellular solute-binding protein | ||
HKNIGPJH_00267 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
HKNIGPJH_00268 | 2.3e-114 | amyE | G | Bacterial extracellular solute-binding protein | ||
HKNIGPJH_00269 | 9.1e-253 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
HKNIGPJH_00270 | 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 | |
HKNIGPJH_00271 | 1.4e-98 | L | Single-strand binding protein family | |||
HKNIGPJH_00272 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HKNIGPJH_00273 | 3.6e-224 | gatB | 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) | |
HKNIGPJH_00274 | 2e-205 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
HKNIGPJH_00275 | 2.1e-51 | S | Protein of unknown function (DUF2469) | |||
HKNIGPJH_00276 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
HKNIGPJH_00277 | 5.7e-51 | S | Psort location CytoplasmicMembrane, score | |||
HKNIGPJH_00278 | 5.9e-235 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
HKNIGPJH_00279 | 2.7e-216 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
HKNIGPJH_00280 | 2.4e-167 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
HKNIGPJH_00281 | 2.3e-92 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HKNIGPJH_00282 | 5.9e-307 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HKNIGPJH_00283 | 3.1e-270 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
HKNIGPJH_00284 | 1.3e-101 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
HKNIGPJH_00285 | 3.9e-92 | 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) | |
HKNIGPJH_00286 | 1.5e-39 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HKNIGPJH_00287 | 6.6e-221 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00288 | 0.0 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00289 | 8e-126 | |||||
HKNIGPJH_00290 | 1.8e-70 | yknV | V | ABC transporter | ||
HKNIGPJH_00291 | 3.2e-155 | 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 |
HKNIGPJH_00292 | 3.4e-35 | |||||
HKNIGPJH_00293 | 1.4e-147 | gluP | 3.4.21.105 | S | Rhomboid family | |
HKNIGPJH_00294 | 3.1e-238 | L | ribosomal rna small subunit methyltransferase | |||
HKNIGPJH_00295 | 1.8e-57 | crgA | D | Involved in cell division | ||
HKNIGPJH_00296 | 7.9e-65 | S | Bacterial protein of unknown function (DUF881) | |||
HKNIGPJH_00297 | 6e-35 | S | Bacterial protein of unknown function (DUF881) | |||
HKNIGPJH_00298 | 5.7e-21 | E | Transglutaminase-like superfamily | |||
HKNIGPJH_00299 | 1.4e-84 | E | Transglutaminase-like superfamily | |||
HKNIGPJH_00300 | 3.1e-220 | S | Protein of unknown function DUF58 | |||
HKNIGPJH_00301 | 2.5e-224 | S | ATPase family associated with various cellular activities (AAA) | |||
HKNIGPJH_00302 | 1.1e-292 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00303 | 8.5e-107 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
HKNIGPJH_00304 | 2.1e-140 | yidP | K | UTRA | ||
HKNIGPJH_00305 | 5.6e-121 | degU | K | helix_turn_helix, Lux Regulon | ||
HKNIGPJH_00306 | 1.7e-264 | tcsS3 | KT | PspC domain | ||
HKNIGPJH_00307 | 4.2e-60 | pspC | KT | PspC domain | ||
HKNIGPJH_00308 | 1.8e-268 | dnaK | O | Heat shock 70 kDa protein | ||
HKNIGPJH_00309 | 2.8e-48 | 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 | ||
HKNIGPJH_00310 | 3.9e-158 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
HKNIGPJH_00311 | 4.5e-115 | hspR | K | transcriptional regulator, MerR family | ||
HKNIGPJH_00312 | 8.6e-47 | |||||
HKNIGPJH_00313 | 3.3e-129 | S | HAD hydrolase, family IA, variant 3 | |||
HKNIGPJH_00314 | 3.4e-29 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00315 | 2.2e-190 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00316 | 0.0 | M | probably involved in cell wall | |||
HKNIGPJH_00317 | 0.0 | S | LPXTG-motif cell wall anchor domain protein | |||
HKNIGPJH_00318 | 2.2e-277 | M | LPXTG-motif cell wall anchor domain protein | |||
HKNIGPJH_00319 | 5.9e-164 | 3.4.22.70 | M | Sortase family | ||
HKNIGPJH_00320 | 3.8e-34 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HKNIGPJH_00321 | 1.9e-56 | 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 | ||
HKNIGPJH_00322 | 1.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HKNIGPJH_00323 | 6.1e-154 | 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 | ||
HKNIGPJH_00324 | 6.8e-47 | 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 | ||
HKNIGPJH_00325 | 1.4e-116 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HKNIGPJH_00326 | 2.3e-116 | 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 | ||
HKNIGPJH_00327 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HKNIGPJH_00328 | 5.9e-199 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HKNIGPJH_00329 | 9.9e-275 | cycA | E | Amino acid permease | ||
HKNIGPJH_00330 | 1.2e-166 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
HKNIGPJH_00331 | 2.6e-129 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
HKNIGPJH_00332 | 1.9e-26 | thiS | 2.8.1.10 | H | ThiS family | |
HKNIGPJH_00333 | 0.0 | S | L,D-transpeptidase catalytic domain | |||
HKNIGPJH_00334 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
HKNIGPJH_00335 | 8.7e-229 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
HKNIGPJH_00336 | 3.2e-57 | I | alpha/beta hydrolase fold | |||
HKNIGPJH_00337 | 3.9e-31 | I | alpha/beta hydrolase fold | |||
HKNIGPJH_00338 | 2.8e-145 | cobB2 | K | Sir2 family | ||
HKNIGPJH_00339 | 4.1e-234 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
HKNIGPJH_00340 | 1.8e-265 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
HKNIGPJH_00341 | 6.3e-268 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
HKNIGPJH_00342 | 4.5e-224 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
HKNIGPJH_00343 | 5e-91 | |||||
HKNIGPJH_00344 | 2.7e-117 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HKNIGPJH_00345 | 1.3e-113 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
HKNIGPJH_00346 | 7.9e-188 | ansA | 3.5.1.1 | EJ | Asparaginase | |
HKNIGPJH_00347 | 0.0 | cadA | P | E1-E2 ATPase | ||
HKNIGPJH_00348 | 1.1e-44 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
HKNIGPJH_00349 | 2.1e-106 | kup | P | Transport of potassium into the cell | ||
HKNIGPJH_00350 | 7.7e-185 | tatD | L | TatD related DNase | ||
HKNIGPJH_00351 | 0.0 | G | Alpha-L-arabinofuranosidase C-terminus | |||
HKNIGPJH_00352 | 2e-178 | S | Endonuclease/Exonuclease/phosphatase family | |||
HKNIGPJH_00353 | 3.9e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HKNIGPJH_00354 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
HKNIGPJH_00355 | 3.6e-108 | 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 | ||
HKNIGPJH_00356 | 2.3e-150 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HKNIGPJH_00357 | 1.4e-104 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
HKNIGPJH_00358 | 2.3e-60 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
HKNIGPJH_00359 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HKNIGPJH_00360 | 7.3e-106 | |||||
HKNIGPJH_00361 | 4.4e-189 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HKNIGPJH_00362 | 1.6e-17 | 3.2.1.78 | GH26 | G | Glycosyl hydrolase family 26 | |
HKNIGPJH_00363 | 3.2e-119 | 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) | |
HKNIGPJH_00364 | 6e-39 | ptsH | G | PTS HPr component phosphorylation site | ||
HKNIGPJH_00365 | 2.7e-183 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00366 | 1.1e-193 | holB | 2.7.7.7 | L | DNA polymerase III | |
HKNIGPJH_00367 | 1.3e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HKNIGPJH_00368 | 4.9e-19 | 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 | |
HKNIGPJH_00369 | 1.7e-119 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
HKNIGPJH_00370 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
HKNIGPJH_00371 | 5.8e-177 | T | Protein tyrosine kinase | |||
HKNIGPJH_00372 | 7.9e-149 | pbpA | M | penicillin-binding protein | ||
HKNIGPJH_00373 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
HKNIGPJH_00374 | 2.4e-164 | MA20_14020 | P | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00375 | 1.5e-186 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00376 | 1.4e-195 | msmE | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | ||
HKNIGPJH_00377 | 7.7e-151 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
HKNIGPJH_00378 | 0.0 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
HKNIGPJH_00379 | 1.8e-234 | malE | G | Bacterial extracellular solute-binding protein | ||
HKNIGPJH_00380 | 3e-101 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HKNIGPJH_00381 | 7.2e-56 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HKNIGPJH_00382 | 6e-120 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HKNIGPJH_00383 | 2.7e-29 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
HKNIGPJH_00384 | 1.2e-279 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HKNIGPJH_00385 | 2.3e-198 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HKNIGPJH_00386 | 2.6e-61 | |||||
HKNIGPJH_00387 | 1.1e-197 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00388 | 1.6e-140 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
HKNIGPJH_00389 | 4.8e-104 | B | Belongs to the OprB family | |||
HKNIGPJH_00390 | 1.1e-101 | T | Forkhead associated domain | |||
HKNIGPJH_00391 | 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 | |
HKNIGPJH_00392 | 1.7e-123 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00393 | 4.4e-164 | G | ABC transporter permease | |||
HKNIGPJH_00394 | 2.8e-171 | 2.7.1.2 | GK | ROK family | ||
HKNIGPJH_00395 | 1.1e-101 | G | Glycosyl hydrolase family 20, domain 2 | |||
HKNIGPJH_00396 | 2.6e-138 | G | Glycosyl hydrolase family 20, domain 2 | |||
HKNIGPJH_00397 | 8e-91 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
HKNIGPJH_00398 | 2.3e-129 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HKNIGPJH_00399 | 1.3e-171 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HKNIGPJH_00400 | 6.8e-203 | parB | K | Belongs to the ParB family | ||
HKNIGPJH_00401 | 1.7e-96 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00402 | 0.0 | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain | |
HKNIGPJH_00403 | 1.5e-115 | S | Protein of unknown function, DUF624 | |||
HKNIGPJH_00404 | 4.5e-73 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
HKNIGPJH_00405 | 0.0 | KLT | Lanthionine synthetase C-like protein | |||
HKNIGPJH_00406 | 6.5e-184 | KLT | serine threonine protein kinase | |||
HKNIGPJH_00407 | 2.6e-135 | 3.6.3.44 | V | ABC transporter | ||
HKNIGPJH_00408 | 1.4e-93 | msbA2 | 3.6.3.44 | V | ABC transporter transmembrane region | |
HKNIGPJH_00409 | 1.6e-176 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
HKNIGPJH_00410 | 1e-256 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HKNIGPJH_00411 | 8.3e-51 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
HKNIGPJH_00412 | 4.1e-69 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
HKNIGPJH_00413 | 5.5e-141 | cpaE | D | bacterial-type flagellum organization | ||
HKNIGPJH_00414 | 6.1e-185 | cpaF | U | Type II IV secretion system protein | ||
HKNIGPJH_00415 | 6.9e-125 | U | Type ii secretion system | |||
HKNIGPJH_00416 | 2.2e-88 | gspF | NU | Type II secretion system (T2SS), protein F | ||
HKNIGPJH_00417 | 0.0 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_00418 | 1.3e-93 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_00419 | 6.2e-34 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_00420 | 3.7e-33 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_00421 | 6e-112 | S | Short C-terminal domain | |||
HKNIGPJH_00422 | 1.1e-61 | S | Protein of unknown function (DUF4230) | |||
HKNIGPJH_00424 | 1.6e-33 | |||||
HKNIGPJH_00425 | 4.2e-38 | |||||
HKNIGPJH_00426 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
HKNIGPJH_00427 | 5.4e-100 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
HKNIGPJH_00428 | 1e-71 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
HKNIGPJH_00429 | 0.0 | G | candidate polyfunctional acetylxylan esterase b-xylosidase A-L-arabinofuranosidase, CBM9 module, glycoside hydrolase family 43 protein and carbohydrate esterase family 6 protein K01238 | |||
HKNIGPJH_00430 | 1.4e-233 | 3.2.1.156 | GH8 | G | CBM9 module, glycoside hydrolase family 8 protein and carbohydrate esterase family 4 protein K01238 | |
HKNIGPJH_00431 | 3.7e-57 | G | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00432 | 6.9e-130 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
HKNIGPJH_00435 | 8.9e-43 | K | Psort location Cytoplasmic, score | |||
HKNIGPJH_00436 | 8.6e-19 | |||||
HKNIGPJH_00438 | 1.2e-129 | |||||
HKNIGPJH_00439 | 3.4e-34 | |||||
HKNIGPJH_00440 | 2.9e-237 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
HKNIGPJH_00441 | 3.5e-133 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
HKNIGPJH_00442 | 4.3e-58 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
HKNIGPJH_00443 | 2.3e-122 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
HKNIGPJH_00444 | 2.3e-44 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HKNIGPJH_00445 | 5.6e-283 | 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 | |
HKNIGPJH_00446 | 1.6e-163 | 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 | ||
HKNIGPJH_00447 | 2.2e-57 | 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 | |
HKNIGPJH_00448 | 2.1e-256 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
HKNIGPJH_00449 | 0.0 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
HKNIGPJH_00450 | 3.7e-134 | 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) | |
HKNIGPJH_00451 | 1e-130 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
HKNIGPJH_00452 | 6.3e-298 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
HKNIGPJH_00453 | 3.8e-240 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
HKNIGPJH_00454 | 1.5e-156 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HKNIGPJH_00455 | 1e-35 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HKNIGPJH_00456 | 9.2e-151 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
HKNIGPJH_00457 | 1.5e-146 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00460 | 2.4e-22 | 2.7.13.3 | T | Histidine kinase | ||
HKNIGPJH_00461 | 1.2e-36 | K | helix_turn_helix, Lux Regulon | |||
HKNIGPJH_00462 | 3e-26 | 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) | |
HKNIGPJH_00463 | 2.7e-144 | yplQ | S | Haemolysin-III related | ||
HKNIGPJH_00464 | 2.6e-80 | 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 | ||
HKNIGPJH_00465 | 1.2e-73 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
HKNIGPJH_00466 | 6.5e-284 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
HKNIGPJH_00467 | 1.1e-45 | |||||
HKNIGPJH_00468 | 1.7e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HKNIGPJH_00469 | 2.4e-116 | |||||
HKNIGPJH_00471 | 0.0 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
HKNIGPJH_00472 | 9.2e-62 | lacY | P | LacY proton/sugar symporter | ||
HKNIGPJH_00473 | 0.0 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
HKNIGPJH_00474 | 8.5e-143 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
HKNIGPJH_00475 | 1.2e-241 | pccB | I | Carboxyl transferase domain | ||
HKNIGPJH_00476 | 1.5e-41 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HKNIGPJH_00477 | 1.5e-83 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HKNIGPJH_00478 | 6.8e-153 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HKNIGPJH_00479 | 7.3e-109 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HKNIGPJH_00480 | 6.9e-130 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
HKNIGPJH_00481 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
HKNIGPJH_00482 | 1.2e-236 | amt | U | Ammonium Transporter Family | ||
HKNIGPJH_00483 | 5.9e-118 | 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) | ||
HKNIGPJH_00484 | 4.1e-251 | 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 | ||
HKNIGPJH_00485 | 5.2e-218 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
HKNIGPJH_00486 | 5.5e-133 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HKNIGPJH_00487 | 7.3e-169 | 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 | ||
HKNIGPJH_00488 | 1.1e-195 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HKNIGPJH_00489 | 8.8e-45 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
HKNIGPJH_00490 | 2e-67 | 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 | |
HKNIGPJH_00491 | 8.8e-83 | mhpC | I | Alpha/beta hydrolase family | ||
HKNIGPJH_00492 | 2.9e-116 | F | Domain of unknown function (DUF4916) | |||
HKNIGPJH_00493 | 6e-61 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
HKNIGPJH_00494 | 1.6e-169 | S | G5 | |||
HKNIGPJH_00495 | 4.6e-88 | |||||
HKNIGPJH_00496 | 2.2e-170 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
HKNIGPJH_00497 | 1.6e-247 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00498 | 1.7e-235 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HKNIGPJH_00499 | 3.3e-62 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
HKNIGPJH_00500 | 2.5e-264 | KLT | Protein tyrosine kinase | |||
HKNIGPJH_00501 | 3.2e-139 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00502 | 3.7e-137 | S | LPXTG-motif cell wall anchor domain protein | |||
HKNIGPJH_00503 | 6.3e-293 | S | LPXTG-motif cell wall anchor domain protein | |||
HKNIGPJH_00504 | 8.1e-84 | 3.2.1.37 | GH43 | G | Glycosyl hydrolases family 43 | |
HKNIGPJH_00505 | 1.1e-239 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
HKNIGPJH_00506 | 2.3e-108 | K | Bacterial regulatory proteins, tetR family | |||
HKNIGPJH_00507 | 1.8e-223 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00508 | 7e-181 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00510 | 9.4e-77 | K | Psort location Cytoplasmic, score | |||
HKNIGPJH_00511 | 4.1e-147 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
HKNIGPJH_00512 | 3e-162 | |||||
HKNIGPJH_00513 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
HKNIGPJH_00514 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
HKNIGPJH_00515 | 3.6e-106 | lacA | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
HKNIGPJH_00516 | 1.5e-155 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
HKNIGPJH_00517 | 2.5e-49 | lipA | I | Hydrolase, alpha beta domain protein | ||
HKNIGPJH_00518 | 0.0 | mdlA2 | V | ABC transporter | ||
HKNIGPJH_00519 | 1.2e-163 | yknV | V | ABC transporter | ||
HKNIGPJH_00520 | 3.8e-63 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
HKNIGPJH_00521 | 4.5e-216 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
HKNIGPJH_00522 | 2.9e-86 | J | TM2 domain | |||
HKNIGPJH_00523 | 8.4e-193 | 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 | |
HKNIGPJH_00524 | 4e-192 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
HKNIGPJH_00525 | 3.9e-137 | ctpE | P | E1-E2 ATPase | ||
HKNIGPJH_00526 | 3.4e-161 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
HKNIGPJH_00527 | 2.6e-167 | ftsE | D | Cell division ATP-binding protein FtsE | ||
HKNIGPJH_00528 | 3.2e-190 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HKNIGPJH_00529 | 1.8e-308 | cbgA_1 | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
HKNIGPJH_00531 | 9.1e-135 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway. Thus, catalyzes the conversion of 4-amino-5-aminomethyl-2-methylpyrimidine to 4-amino- 5-hydroxymethyl-2-methylpyrimidine (HMP) | |
HKNIGPJH_00532 | 1.3e-223 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00533 | 1.2e-176 | yjjP | S | Threonine/Serine exporter, ThrE | ||
HKNIGPJH_00534 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HKNIGPJH_00535 | 8e-196 | S | Uncharacterized conserved protein (DUF2183) | |||
HKNIGPJH_00536 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
HKNIGPJH_00537 | 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 | |
HKNIGPJH_00538 | 3.4e-156 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
HKNIGPJH_00539 | 4.9e-81 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
HKNIGPJH_00540 | 0.0 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
HKNIGPJH_00541 | 4.9e-49 | O | Thioredoxin | |||
HKNIGPJH_00542 | 0.0 | KLT | Protein tyrosine kinase | |||
HKNIGPJH_00543 | 1e-46 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
HKNIGPJH_00544 | 4.4e-237 | G | MFS/sugar transport protein | |||
HKNIGPJH_00545 | 1.4e-117 | 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 | |
HKNIGPJH_00546 | 1.7e-137 | lmrA2 | V | ABC transporter transmembrane region | ||
HKNIGPJH_00547 | 6.7e-26 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
HKNIGPJH_00548 | 1.8e-52 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
HKNIGPJH_00549 | 1.6e-187 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
HKNIGPJH_00550 | 1.2e-36 | |||||
HKNIGPJH_00551 | 1.3e-97 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
HKNIGPJH_00552 | 5.3e-251 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
HKNIGPJH_00553 | 3.4e-97 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
HKNIGPJH_00554 | 7.6e-129 | E | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00555 | 1.4e-133 | yebE | S | DUF218 domain | ||
HKNIGPJH_00556 | 5.3e-106 | 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 | ||
HKNIGPJH_00557 | 5.3e-41 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
HKNIGPJH_00558 | 3.6e-63 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
HKNIGPJH_00559 | 8e-188 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HKNIGPJH_00560 | 2.7e-91 | mraZ | K | Belongs to the MraZ family | ||
HKNIGPJH_00561 | 5.5e-10 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HKNIGPJH_00562 | 3.3e-57 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HKNIGPJH_00563 | 1.4e-29 | E | Receptor family ligand binding region | |||
HKNIGPJH_00564 | 1.1e-195 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00565 | 1.3e-158 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
HKNIGPJH_00566 | 6.1e-86 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HKNIGPJH_00567 | 8.1e-203 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
HKNIGPJH_00568 | 1.4e-215 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
HKNIGPJH_00569 | 7.3e-101 | K | Bacterial regulatory proteins, tetR family | |||
HKNIGPJH_00570 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
HKNIGPJH_00571 | 3.1e-62 | K | Bacterial regulatory proteins, tetR family | |||
HKNIGPJH_00572 | 3.8e-75 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
HKNIGPJH_00573 | 2.6e-109 | S | LytR cell envelope-related transcriptional attenuator | |||
HKNIGPJH_00574 | 1.1e-167 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
HKNIGPJH_00575 | 1.3e-165 | ksgA | 2.1.1.182, 2.1.1.184 | 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 | |
HKNIGPJH_00576 | 4e-39 | S | G5 | |||
HKNIGPJH_00577 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00578 | 3e-206 | abfA1 | 3.2.1.55 | GH51 | G | arabinose metabolic process |
HKNIGPJH_00579 | 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 | ||
HKNIGPJH_00580 | 2.7e-134 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HKNIGPJH_00581 | 3.4e-137 | fmt | 2.1.1.176, 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 | |
HKNIGPJH_00582 | 2.9e-145 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HKNIGPJH_00583 | 1.4e-242 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00584 | 6.8e-112 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00585 | 1.2e-32 | S | Uncharacterised protein family (UPF0182) | |||
HKNIGPJH_00586 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
HKNIGPJH_00587 | 6.8e-83 | S | Lysylphosphatidylglycerol synthase TM region | |||
HKNIGPJH_00588 | 3e-35 | S | Lysylphosphatidylglycerol synthase TM region | |||
HKNIGPJH_00589 | 1.6e-279 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
HKNIGPJH_00590 | 2.1e-11 | S | PGAP1-like protein | |||
HKNIGPJH_00591 | 2.6e-79 | 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 | |
HKNIGPJH_00592 | 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 | |
HKNIGPJH_00593 | 2.7e-255 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
HKNIGPJH_00594 | 1.6e-123 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
HKNIGPJH_00595 | 3.3e-146 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
HKNIGPJH_00596 | 1.2e-45 | aspB | E | Aminotransferase class-V | ||
HKNIGPJH_00597 | 3e-168 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HKNIGPJH_00598 | 2.2e-99 | tmp1 | S | Domain of unknown function (DUF4391) | ||
HKNIGPJH_00600 | 6.1e-82 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
HKNIGPJH_00601 | 9e-95 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
HKNIGPJH_00602 | 1.9e-112 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
HKNIGPJH_00603 | 2.5e-13 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HKNIGPJH_00604 | 1.9e-40 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HKNIGPJH_00605 | 6.5e-85 | G | Transporter major facilitator family protein | |||
HKNIGPJH_00606 | 6e-195 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HKNIGPJH_00607 | 2.8e-105 | K | Bacterial regulatory proteins, tetR family | |||
HKNIGPJH_00608 | 1.1e-102 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
HKNIGPJH_00609 | 1.2e-126 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HKNIGPJH_00610 | 2.3e-176 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
HKNIGPJH_00611 | 2.1e-149 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
HKNIGPJH_00612 | 1.9e-106 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HKNIGPJH_00613 | 3e-251 | T | GHKL domain | |||
HKNIGPJH_00614 | 7.2e-152 | T | LytTr DNA-binding domain | |||
HKNIGPJH_00615 | 8.2e-37 | S | Calcineurin-like phosphoesterase | |||
HKNIGPJH_00616 | 1.1e-139 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
HKNIGPJH_00617 | 3.5e-271 | 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 | |
HKNIGPJH_00618 | 2.2e-35 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
HKNIGPJH_00619 | 5.5e-175 | S | Protein of unknown function DUF58 | |||
HKNIGPJH_00620 | 1.4e-90 | |||||
HKNIGPJH_00621 | 4.7e-191 | S | von Willebrand factor (vWF) type A domain | |||
HKNIGPJH_00622 | 8.8e-57 | S | von Willebrand factor (vWF) type A domain | |||
HKNIGPJH_00623 | 0.0 | S | Protein of unknown function (DUF975) | |||
HKNIGPJH_00624 | 8.6e-137 | S | Putative ABC-transporter type IV | |||
HKNIGPJH_00625 | 7.1e-39 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HKNIGPJH_00626 | 4.5e-163 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
HKNIGPJH_00627 | 8.2e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
HKNIGPJH_00628 | 1.8e-248 | 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 | |
HKNIGPJH_00629 | 1.3e-14 | |||||
HKNIGPJH_00630 | 1.2e-20 | |||||
HKNIGPJH_00631 | 3.1e-74 | 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 | |
HKNIGPJH_00632 | 3.5e-252 | yhjE | EGP | Sugar (and other) transporter | ||
HKNIGPJH_00633 | 5.6e-103 | scrT | G | Transporter major facilitator family protein | ||
HKNIGPJH_00634 | 2.6e-21 | rmuC | S | RmuC family | ||
HKNIGPJH_00635 | 4.4e-134 | 3.6.3.3, 3.6.3.5, 3.6.3.54 | P | Heavy metal translocating P-type atpase | ||
HKNIGPJH_00636 | 3.9e-276 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
HKNIGPJH_00637 | 1.5e-71 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
HKNIGPJH_00638 | 9.7e-222 | |||||
HKNIGPJH_00639 | 4.2e-89 | S | Glycosyl transferase, family 2 | |||
HKNIGPJH_00640 | 1.1e-36 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00641 | 4e-153 | rafG | G | ABC transporter permease | ||
HKNIGPJH_00642 | 5.8e-106 | S | Protein of unknown function, DUF624 | |||
HKNIGPJH_00643 | 2.9e-13 | S | Transposon-encoded protein TnpV | |||
HKNIGPJH_00644 | 9.7e-109 | pepE | 3.4.13.21 | E | Peptidase family S51 | |
HKNIGPJH_00645 | 5.5e-48 | U | TadE-like protein | |||
HKNIGPJH_00646 | 1.1e-54 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
HKNIGPJH_00647 | 4.9e-218 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
HKNIGPJH_00648 | 1.6e-193 | S | Psort location CytoplasmicMembrane, score | |||
HKNIGPJH_00649 | 1.1e-96 | K | Bacterial regulatory proteins, tetR family | |||
HKNIGPJH_00650 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
HKNIGPJH_00651 | 2.2e-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 | ||
HKNIGPJH_00652 | 3.4e-135 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
HKNIGPJH_00653 | 1.4e-96 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
HKNIGPJH_00654 | 3.9e-209 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
HKNIGPJH_00655 | 2.4e-115 | |||||
HKNIGPJH_00656 | 3.7e-301 | S | Calcineurin-like phosphoesterase | |||
HKNIGPJH_00657 | 1.1e-135 | 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) | |
HKNIGPJH_00658 | 1.7e-161 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
HKNIGPJH_00659 | 4.9e-176 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HKNIGPJH_00660 | 4.3e-87 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HKNIGPJH_00661 | 4.6e-19 | 3.1.21.3 | V | DivIVA protein | ||
HKNIGPJH_00662 | 1.7e-31 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
HKNIGPJH_00663 | 3.4e-121 | ybjG | 3.6.1.27 | I | Psort location CytoplasmicMembrane, score | |
HKNIGPJH_00664 | 2.1e-81 | ypeA | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00665 | 1.1e-113 | vex2 | V | ABC transporter, ATP-binding protein | ||
HKNIGPJH_00666 | 4.3e-11 | uspA | T | Belongs to the universal stress protein A family | ||
HKNIGPJH_00667 | 1.2e-182 | S | Protein of unknown function (DUF3027) | |||
HKNIGPJH_00668 | 4.5e-67 | cspB | K | 'Cold-shock' DNA-binding domain | ||
HKNIGPJH_00669 | 5.6e-203 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
HKNIGPJH_00670 | 3.8e-45 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00671 | 7.6e-46 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00672 | 2.7e-52 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00673 | 4.1e-23 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00674 | 3.7e-67 | S | Fibronectin type 3 domain | |||
HKNIGPJH_00675 | 6.4e-102 | yghZ | C | Aldo/keto reductase family | ||
HKNIGPJH_00676 | 3.2e-58 | S | Protein of unknown function (DUF3039) | |||
HKNIGPJH_00677 | 7.7e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HKNIGPJH_00678 | 8.5e-134 | |||||
HKNIGPJH_00679 | 1.8e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
HKNIGPJH_00680 | 1e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HKNIGPJH_00681 | 5.7e-136 | 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 | |
HKNIGPJH_00682 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
HKNIGPJH_00683 | 2.8e-91 | ilvN | 2.2.1.6 | E | ACT domain | |
HKNIGPJH_00684 | 3e-93 | |||||
HKNIGPJH_00685 | 0.0 | yjjK | S | ABC transporter | ||
HKNIGPJH_00686 | 1.6e-151 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
HKNIGPJH_00687 | 1e-301 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HKNIGPJH_00688 | 1.6e-94 | |||||
HKNIGPJH_00693 | 3.3e-101 | S | Protein of unknown function DUF45 | |||
HKNIGPJH_00694 | 1.4e-184 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
HKNIGPJH_00695 | 2.4e-98 | ytfL | P | Transporter associated domain | ||
HKNIGPJH_00696 | 8.7e-67 | prs | 2.7.6.1 | F | Belongs to the ribose-phosphate pyrophosphokinase family | |
HKNIGPJH_00697 | 4.4e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HKNIGPJH_00698 | 4.5e-149 | 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 | ||
HKNIGPJH_00699 | 3.3e-106 | 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 | |
HKNIGPJH_00700 | 1.7e-57 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
HKNIGPJH_00701 | 5.2e-19 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
HKNIGPJH_00702 | 1e-161 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
HKNIGPJH_00703 | 2.1e-114 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
HKNIGPJH_00704 | 2.7e-185 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HKNIGPJH_00705 | 2.2e-162 | M | Bacterial capsule synthesis protein PGA_cap | |||
HKNIGPJH_00706 | 6.5e-51 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
HKNIGPJH_00707 | 7.1e-281 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00708 | 1.6e-207 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
HKNIGPJH_00712 | 7.7e-171 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
HKNIGPJH_00713 | 4e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
HKNIGPJH_00714 | 1.2e-154 | ypfH | S | Phospholipase/Carboxylesterase | ||
HKNIGPJH_00715 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
HKNIGPJH_00716 | 1.4e-77 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HKNIGPJH_00717 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
HKNIGPJH_00718 | 1.5e-230 | nagC | GK | ROK family | ||
HKNIGPJH_00719 | 1.5e-244 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
HKNIGPJH_00720 | 6.6e-157 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00721 | 2.6e-155 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_00722 | 1.4e-110 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
HKNIGPJH_00723 | 3.2e-107 | G | Transmembrane secretion effector | |||
HKNIGPJH_00724 | 4.5e-14 | V | MATE efflux family protein | |||
HKNIGPJH_00726 | 3.6e-268 | S | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00727 | 5.8e-17 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
HKNIGPJH_00728 | 2.7e-41 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
HKNIGPJH_00729 | 3.8e-195 | S | alpha beta | |||
HKNIGPJH_00730 | 1.3e-25 | yhjX | EGP | Major facilitator Superfamily | ||
HKNIGPJH_00731 | 9.4e-35 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00733 | 7.1e-43 | gcvR | T | Belongs to the UPF0237 family | ||
HKNIGPJH_00734 | 1.1e-23 | lmrB | EGP | Major facilitator Superfamily | ||
HKNIGPJH_00735 | 1.5e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
HKNIGPJH_00736 | 1.5e-143 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
HKNIGPJH_00737 | 6e-76 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
HKNIGPJH_00738 | 5.9e-230 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
HKNIGPJH_00739 | 3.6e-195 | |||||
HKNIGPJH_00740 | 2.7e-180 | |||||
HKNIGPJH_00741 | 5.9e-120 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HKNIGPJH_00742 | 2.1e-137 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HKNIGPJH_00743 | 5e-128 | V | ATPases associated with a variety of cellular activities | |||
HKNIGPJH_00744 | 1.7e-75 | E | ABC transporter, substrate-binding protein, family 5 | |||
HKNIGPJH_00745 | 8.7e-133 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
HKNIGPJH_00746 | 1.6e-26 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
HKNIGPJH_00747 | 9.9e-160 | S | Patatin-like phospholipase | |||
HKNIGPJH_00749 | 2.1e-39 | S | Tetratricopeptide repeat | |||
HKNIGPJH_00750 | 2e-17 | S | Tetratricopeptide repeat | |||
HKNIGPJH_00751 | 6.9e-104 | S | Tetratricopeptide repeat | |||
HKNIGPJH_00752 | 2.7e-45 | S | Tetratricopeptide repeat | |||
HKNIGPJH_00753 | 6.5e-249 | cydD | V | ABC transporter transmembrane region | ||
HKNIGPJH_00754 | 1.5e-35 | rpmE | J | Binds the 23S rRNA | ||
HKNIGPJH_00756 | 6.8e-226 | xylR | GK | ROK family | ||
HKNIGPJH_00757 | 2.1e-118 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_00758 | 2.1e-88 | K | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00759 | 1.1e-61 | S | FMN_bind | |||
HKNIGPJH_00760 | 1.6e-143 | macB | V | ABC transporter, ATP-binding protein | ||
HKNIGPJH_00761 | 2.3e-93 | pilT | NU | Type II/IV secretion system protein | ||
HKNIGPJH_00762 | 0.0 | |||||
HKNIGPJH_00763 | 4e-62 | scrT | G | Transporter major facilitator family protein | ||
HKNIGPJH_00764 | 1.6e-149 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00765 | 2.4e-161 | amyD3 | P | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_00766 | 2.5e-28 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00767 | 2.7e-41 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
HKNIGPJH_00768 | 2.3e-45 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
HKNIGPJH_00769 | 2.6e-177 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HKNIGPJH_00770 | 2.4e-32 | secG | U | Preprotein translocase SecG subunit | ||
HKNIGPJH_00771 | 1.6e-249 | 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 | |
HKNIGPJH_00772 | 9.5e-200 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
HKNIGPJH_00773 | 3e-10 | |||||
HKNIGPJH_00774 | 2.6e-300 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
HKNIGPJH_00775 | 5.6e-59 | |||||
HKNIGPJH_00776 | 2.1e-260 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00777 | 3.9e-187 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_00778 | 0.0 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
HKNIGPJH_00779 | 2.2e-37 | 4.2.1.53 | S | MCRA family | ||
HKNIGPJH_00780 | 9.1e-155 | 4.2.1.53 | S | MCRA family | ||
HKNIGPJH_00781 | 3.3e-89 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HKNIGPJH_00782 | 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) | |
HKNIGPJH_00783 | 5.9e-266 | 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) | |
HKNIGPJH_00784 | 1.6e-141 | S | Bacterial protein of unknown function (DUF881) | |||
HKNIGPJH_00785 | 4.2e-45 | sbp | S | Protein of unknown function (DUF1290) | ||
HKNIGPJH_00786 | 1.7e-44 | M | Mechanosensitive ion channel | |||
HKNIGPJH_00787 | 1.1e-177 | S | CAAX protease self-immunity | |||
HKNIGPJH_00788 | 2.6e-214 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
HKNIGPJH_00789 | 0.0 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
HKNIGPJH_00790 | 1.6e-102 | 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 | ||
HKNIGPJH_00791 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HKNIGPJH_00792 | 2e-56 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
HKNIGPJH_00793 | 3.9e-190 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
HKNIGPJH_00794 | 2.2e-96 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HKNIGPJH_00795 | 0.0 | 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 | |
HKNIGPJH_00796 | 4.1e-23 | XK27_06785 | V | ABC transporter | ||
HKNIGPJH_00797 | 8.8e-160 | yicL | EG | EamA-like transporter family | ||
HKNIGPJH_00798 | 3.9e-193 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
HKNIGPJH_00799 | 4.1e-71 | lmrA2 | V | ABC transporter transmembrane region | ||
HKNIGPJH_00800 | 2.9e-257 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
HKNIGPJH_00801 | 1.7e-61 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
HKNIGPJH_00802 | 2.4e-133 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
HKNIGPJH_00803 | 1.1e-150 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HKNIGPJH_00804 | 3e-60 | S | Thiamine-binding protein | |||
HKNIGPJH_00805 | 1.7e-151 | S | Protein of unknown function (DUF3710) | |||
HKNIGPJH_00806 | 1.4e-172 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
HKNIGPJH_00807 | 1.3e-48 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
HKNIGPJH_00808 | 8.3e-42 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
HKNIGPJH_00809 | 7.8e-148 | S | phosphoesterase or phosphohydrolase | |||
HKNIGPJH_00810 | 2.5e-128 | |||||
HKNIGPJH_00811 | 1.1e-189 | eccCa | D | FtsK/SpoIIIE family | ||
HKNIGPJH_00812 | 1e-254 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HKNIGPJH_00813 | 1.1e-79 | lmrB | U | Major Facilitator Superfamily | ||
HKNIGPJH_00814 | 1.4e-43 | K | helix_turn_helix, mercury resistance | |||
HKNIGPJH_00815 | 6.3e-14 | K | helix_turn_helix, mercury resistance | |||
HKNIGPJH_00816 | 2.9e-87 | K | Periplasmic binding protein domain | |||
HKNIGPJH_00817 | 3.4e-54 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
HKNIGPJH_00818 | 3.2e-152 | S | Glycosyl transferase, family 2 | |||
HKNIGPJH_00819 | 6.7e-51 | S | Glycosyl transferase, family 2 | |||
HKNIGPJH_00820 | 8.9e-300 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
HKNIGPJH_00821 | 2.5e-203 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
HKNIGPJH_00822 | 1.8e-215 | ybiR | P | Citrate transporter | ||
HKNIGPJH_00823 | 1.2e-169 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HKNIGPJH_00824 | 4.9e-139 | 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 | |
HKNIGPJH_00825 | 4.5e-205 | 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 | |
HKNIGPJH_00826 | 1.5e-87 | |||||
HKNIGPJH_00827 | 5.6e-92 | gltX | 6.1.1.17 | 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) | |
HKNIGPJH_00828 | 3.6e-31 | S | Protein of unknown function (DUF805) | |||
HKNIGPJH_00829 | 3.6e-139 | M | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses | |||
HKNIGPJH_00830 | 5.6e-219 | S | Domain of unknown function (DUF5067) | |||
HKNIGPJH_00833 | 4.4e-223 | 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 | |
HKNIGPJH_00834 | 1.9e-127 | gntR | K | FCD | ||
HKNIGPJH_00835 | 5.6e-79 | gntK | 2.7.1.12 | F | Shikimate kinase | |
HKNIGPJH_00836 | 2e-76 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00837 | 3.1e-62 | kup | P | Transport of potassium into the cell | ||
HKNIGPJH_00838 | 2.3e-167 | S | Glutamine amidotransferase domain | |||
HKNIGPJH_00839 | 9.6e-149 | T | HD domain | |||
HKNIGPJH_00840 | 7.5e-63 | lmrB | U | Major Facilitator Superfamily | ||
HKNIGPJH_00841 | 4.6e-158 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
HKNIGPJH_00842 | 7.8e-56 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
HKNIGPJH_00843 | 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 | ||
HKNIGPJH_00844 | 1.1e-17 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HKNIGPJH_00845 | 1.1e-197 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
HKNIGPJH_00847 | 2.2e-49 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
HKNIGPJH_00848 | 2.2e-16 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
HKNIGPJH_00849 | 2.2e-128 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
HKNIGPJH_00850 | 3.9e-156 | hgdC | I | BadF/BadG/BcrA/BcrD ATPase family | ||
HKNIGPJH_00851 | 6.1e-191 | nusA | K | Participates in both transcription termination and antitermination | ||
HKNIGPJH_00852 | 2e-102 | |||||
HKNIGPJH_00854 | 5.7e-45 | E | Transglutaminase/protease-like homologues | |||
HKNIGPJH_00855 | 1.3e-50 | lhr | L | DEAD DEAH box helicase | ||
HKNIGPJH_00856 | 8.3e-102 | lhr | L | DEAD DEAH box helicase | ||
HKNIGPJH_00857 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
HKNIGPJH_00858 | 1.3e-66 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
HKNIGPJH_00859 | 1.3e-190 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
HKNIGPJH_00860 | 4.4e-103 | |||||
HKNIGPJH_00861 | 4.5e-21 | typA | T | Elongation factor G C-terminus | ||
HKNIGPJH_00862 | 8.8e-177 | 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 | ||
HKNIGPJH_00863 | 2.6e-39 | rpmA | J | Ribosomal L27 protein | ||
HKNIGPJH_00864 | 2.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HKNIGPJH_00865 | 8.5e-72 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
HKNIGPJH_00866 | 2.1e-285 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
HKNIGPJH_00867 | 2.1e-137 | luxE | 6.2.1.19 | H | long-chain-fatty-acid--luciferin-component ligase, acyl-protein synthase | |
HKNIGPJH_00868 | 3.6e-85 | ptpA | 3.1.3.48 | T | low molecular weight | |
HKNIGPJH_00869 | 2.4e-129 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
HKNIGPJH_00870 | 3.8e-181 | 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 | |
HKNIGPJH_00871 | 7.3e-206 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
HKNIGPJH_00872 | 2.8e-79 | K | helix_turn_helix ASNC type | |||
HKNIGPJH_00873 | 5.3e-215 | V | FtsX-like permease family | |||
HKNIGPJH_00874 | 1.9e-150 | lolD | V | ABC transporter | ||
HKNIGPJH_00875 | 6.1e-257 | 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 |
HKNIGPJH_00876 | 8.2e-63 | I | Sterol carrier protein | |||
HKNIGPJH_00877 | 3.4e-141 | glpR | K | DeoR C terminal sensor domain | ||
HKNIGPJH_00878 | 8.8e-228 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
HKNIGPJH_00879 | 1.9e-89 | S | Vitamin K epoxide reductase | |||
HKNIGPJH_00880 | 7.8e-171 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine | |
HKNIGPJH_00881 | 2.2e-145 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HKNIGPJH_00882 | 4.8e-28 | 5.3.1.27 | G | SIS domain | ||
HKNIGPJH_00883 | 0.0 | V | ABC transporter transmembrane region | |||
HKNIGPJH_00885 | 5.4e-181 | S | Auxin Efflux Carrier | |||
HKNIGPJH_00886 | 9.7e-52 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HKNIGPJH_00887 | 3.6e-88 | 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 | |
HKNIGPJH_00888 | 9e-72 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
HKNIGPJH_00889 | 6.1e-108 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
HKNIGPJH_00890 | 6.7e-18 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
HKNIGPJH_00891 | 2.7e-166 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
HKNIGPJH_00892 | 1.2e-132 | V | Efflux ABC transporter, permease protein | |||
HKNIGPJH_00893 | 4.5e-16 | |||||
HKNIGPJH_00894 | 1.9e-121 | recX | S | Modulates RecA activity | ||
HKNIGPJH_00895 | 2.6e-189 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
HKNIGPJH_00896 | 3.4e-55 | DJ | Addiction module toxin, RelE StbE family | |||
HKNIGPJH_00897 | 1.3e-48 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
HKNIGPJH_00898 | 1.7e-125 | S | Short repeat of unknown function (DUF308) | |||
HKNIGPJH_00899 | 1.9e-17 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_00900 | 6.2e-103 | S | Domain of unknown function (DUF4037) | |||
HKNIGPJH_00901 | 9.6e-35 | S | Domain of unknown function (DUF4037) | |||
HKNIGPJH_00902 | 7e-37 | araJ | EGP | Major facilitator Superfamily | ||
HKNIGPJH_00903 | 1.7e-218 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
HKNIGPJH_00904 | 1.7e-198 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HKNIGPJH_00905 | 1.1e-25 | pflA | S | Protein of unknown function (DUF4012) | ||
HKNIGPJH_00906 | 9.1e-25 | pflA | S | Protein of unknown function (DUF4012) | ||
HKNIGPJH_00907 | 5.2e-181 | rhaR_1 | K | helix_turn_helix, arabinose operon control protein | ||
HKNIGPJH_00908 | 9.5e-197 | Z012_01000 | 1.1.1.14, 1.1.1.9 | C | Zinc-binding dehydrogenase | |
HKNIGPJH_00909 | 1.9e-250 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_00910 | 1.3e-215 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
HKNIGPJH_00911 | 3.2e-76 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
HKNIGPJH_00912 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HKNIGPJH_00913 | 3.4e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HKNIGPJH_00914 | 2.4e-80 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HKNIGPJH_00915 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
HKNIGPJH_00916 | 3.4e-26 | |||||
HKNIGPJH_00917 | 2.2e-246 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00918 | 2.1e-106 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_00919 | 1.2e-42 | 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 | |
HKNIGPJH_00920 | 2.3e-129 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
HKNIGPJH_00921 | 1.6e-151 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
HKNIGPJH_00922 | 5.1e-134 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
HKNIGPJH_00923 | 9.2e-142 | ybbL | V | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_00924 | 1.7e-218 | GK | ROK family | |||
HKNIGPJH_00925 | 1.5e-43 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
HKNIGPJH_00926 | 2.4e-62 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
HKNIGPJH_00927 | 6.6e-224 | 2.7.13.3 | T | Histidine kinase | ||
HKNIGPJH_00928 | 4.7e-67 | K | helix_turn_helix, Lux Regulon | |||
HKNIGPJH_00929 | 8.6e-31 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
HKNIGPJH_00930 | 4e-156 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | 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 | |
HKNIGPJH_00931 | 4.7e-45 | L | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_00932 | 4.5e-50 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
HKNIGPJH_00934 | 5.7e-172 | corA | P | CorA-like Mg2+ transporter protein | ||
HKNIGPJH_00935 | 1.5e-163 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
HKNIGPJH_00936 | 4.7e-174 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HKNIGPJH_00937 | 1.5e-142 | rnj | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HKNIGPJH_00938 | 1.3e-227 | rutG | F | Permease family | ||
HKNIGPJH_00939 | 8.2e-45 | S | Nucleotidyltransferase domain | |||
HKNIGPJH_00940 | 1.4e-130 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
HKNIGPJH_00941 | 3.1e-264 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
HKNIGPJH_00942 | 3e-128 | V | ABC transporter | |||
HKNIGPJH_00943 | 1.1e-62 | V | ABC transporter permease | |||
HKNIGPJH_00944 | 4.6e-137 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
HKNIGPJH_00945 | 1.2e-112 | I | acetylesterase activity | |||
HKNIGPJH_00946 | 5e-54 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
HKNIGPJH_00947 | 3e-150 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
HKNIGPJH_00948 | 3.2e-88 | naiP | U | Sugar (and other) transporter | ||
HKNIGPJH_00950 | 2.1e-253 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
HKNIGPJH_00951 | 3.4e-106 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
HKNIGPJH_00952 | 5e-145 | bioM | P | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_00953 | 1.8e-113 | E | Aminotransferase class I and II | |||
HKNIGPJH_00954 | 2.9e-72 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
HKNIGPJH_00955 | 3e-139 | hisF | 4.1.3.27 | 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 | |
HKNIGPJH_00956 | 5.4e-124 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
HKNIGPJH_00957 | 1.1e-59 | P | NMT1/THI5 like | |||
HKNIGPJH_00958 | 2.8e-214 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
HKNIGPJH_00959 | 4.1e-28 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HKNIGPJH_00960 | 2.6e-09 | G | Transmembrane secretion effector | |||
HKNIGPJH_00961 | 3.5e-120 | K | Bacterial regulatory proteins, tetR family | |||
HKNIGPJH_00962 | 1.1e-39 | nrdH | O | Glutaredoxin | ||
HKNIGPJH_00963 | 3.3e-74 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
HKNIGPJH_00964 | 1.1e-153 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HKNIGPJH_00965 | 2.7e-70 | 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 | |
HKNIGPJH_00966 | 3.5e-103 | 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 | |
HKNIGPJH_00967 | 1.3e-190 | T | Universal stress protein family | |||
HKNIGPJH_00968 | 1.3e-79 | M | NlpC/P60 family | |||
HKNIGPJH_00969 | 4.1e-86 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
HKNIGPJH_00970 | 1.3e-182 | S | Endonuclease/Exonuclease/phosphatase family | |||
HKNIGPJH_00971 | 1.3e-235 | 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 | ||
HKNIGPJH_00972 | 3.4e-112 | 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 | |
HKNIGPJH_00974 | 3.9e-246 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
HKNIGPJH_00975 | 1.7e-16 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
HKNIGPJH_00976 | 3.4e-48 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
HKNIGPJH_00977 | 1.7e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
HKNIGPJH_00978 | 3.5e-244 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
HKNIGPJH_00979 | 4.8e-156 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
HKNIGPJH_00980 | 2.3e-284 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
HKNIGPJH_00981 | 1.3e-210 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HKNIGPJH_00982 | 5.7e-54 | M | Protein of unknown function (DUF3152) | |||
HKNIGPJH_00983 | 1.3e-299 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
HKNIGPJH_00984 | 2.2e-34 | crr | G | pts system, glucose-specific IIABC component | ||
HKNIGPJH_00985 | 9.2e-82 | |||||
HKNIGPJH_00986 | 3.2e-79 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
HKNIGPJH_00987 | 8.5e-218 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
HKNIGPJH_00988 | 2.7e-227 | 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 | ||
HKNIGPJH_00989 | 6e-100 | 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 | |
HKNIGPJH_00990 | 7.9e-20 | T | helix_turn_helix, Lux Regulon | |||
HKNIGPJH_00991 | 1.6e-30 | 2.7.13.3 | T | Histidine kinase | ||
HKNIGPJH_00992 | 1.6e-39 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
HKNIGPJH_00993 | 1.3e-99 | yjjP | S | Threonine/Serine exporter, ThrE | ||
HKNIGPJH_00994 | 6.1e-170 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
HKNIGPJH_00995 | 4.3e-21 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HKNIGPJH_00996 | 7.7e-22 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HKNIGPJH_00997 | 1.4e-264 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
HKNIGPJH_00998 | 0.0 | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
HKNIGPJH_00999 | 2.7e-229 | P | Sodium/hydrogen exchanger family | |||
HKNIGPJH_01000 | 0.0 | V | FtsX-like permease family | |||
HKNIGPJH_01001 | 5.4e-270 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
HKNIGPJH_01002 | 8.3e-12 | S | Protein of unknown function, DUF624 | |||
HKNIGPJH_01003 | 2.5e-189 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_01004 | 4.9e-39 | G | beta-mannosidase | |||
HKNIGPJH_01005 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
HKNIGPJH_01006 | 1.6e-60 | 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 | |
HKNIGPJH_01007 | 5.2e-15 | |||||
HKNIGPJH_01008 | 1.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
HKNIGPJH_01009 | 7.8e-174 | V | ATPases associated with a variety of cellular activities | |||
HKNIGPJH_01010 | 1.1e-98 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
HKNIGPJH_01011 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
HKNIGPJH_01012 | 9.2e-197 | D | FtsK/SpoIIIE family | |||
HKNIGPJH_01013 | 9.5e-113 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
HKNIGPJH_01014 | 1.9e-146 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
HKNIGPJH_01015 | 9.2e-29 | 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 | |
HKNIGPJH_01016 | 2.3e-19 | V | Beta-lactamase | |||
HKNIGPJH_01017 | 9.3e-74 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HKNIGPJH_01018 | 2.1e-57 | ribD | 1.1.1.193, 3.5.4.26 | H | Cytidine and deoxycytidylate deaminase zinc-binding region | |
HKNIGPJH_01019 | 4e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
HKNIGPJH_01020 | 1.3e-67 | cydD | V | ABC transporter transmembrane region | ||
HKNIGPJH_01022 | 3.7e-265 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HKNIGPJH_01023 | 1.9e-109 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
HKNIGPJH_01024 | 2.8e-121 | |||||
HKNIGPJH_01025 | 5.9e-77 | 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 | ||
HKNIGPJH_01026 | 2.3e-108 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
HKNIGPJH_01027 | 1.1e-181 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
HKNIGPJH_01028 | 9.2e-15 | 3.1.21.3 | V | DivIVA protein | ||
HKNIGPJH_01029 | 6.9e-41 | yggT | S | YGGT family | ||
HKNIGPJH_01030 | 8.9e-81 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
HKNIGPJH_01031 | 1e-31 | 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 | ||
HKNIGPJH_01032 | 1.7e-22 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
HKNIGPJH_01033 | 5.8e-143 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
HKNIGPJH_01034 | 4e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HKNIGPJH_01035 | 3.8e-84 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HKNIGPJH_01036 | 7.9e-263 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
HKNIGPJH_01037 | 4e-53 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_01038 | 9.1e-30 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_01039 | 0.0 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
HKNIGPJH_01040 | 2e-33 | 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 | |
HKNIGPJH_01041 | 1.3e-221 | aroG | 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) | |
HKNIGPJH_01042 | 1.6e-61 | aroG | 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) | |
HKNIGPJH_01043 | 5.3e-40 | GK | ROK family | |||
HKNIGPJH_01044 | 2.7e-198 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
HKNIGPJH_01045 | 1e-284 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HKNIGPJH_01046 | 5.5e-74 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HKNIGPJH_01047 | 1.4e-18 | argR | K | Regulates arginine biosynthesis genes | ||
HKNIGPJH_01048 | 3.8e-55 | argR | K | Regulates arginine biosynthesis genes | ||
HKNIGPJH_01049 | 1.5e-126 | 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 | |
HKNIGPJH_01050 | 1.6e-140 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
HKNIGPJH_01051 | 1.2e-169 | proP | EGP | Sugar (and other) transporter | ||
HKNIGPJH_01053 | 2.9e-58 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
HKNIGPJH_01054 | 1.5e-65 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01055 | 1.7e-182 | K | Psort location Cytoplasmic, score | |||
HKNIGPJH_01056 | 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 | ||
HKNIGPJH_01057 | 1e-37 | 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 | |
HKNIGPJH_01058 | 4.5e-172 | 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 | |
HKNIGPJH_01059 | 2.5e-42 | S | Protein of unknown function (DUF721) | |||
HKNIGPJH_01060 | 4.3e-31 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
HKNIGPJH_01061 | 3.4e-43 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
HKNIGPJH_01062 | 5.4e-121 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
HKNIGPJH_01063 | 2.8e-13 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01064 | 1.7e-199 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01065 | 7.3e-47 | arc | O | AAA ATPase forming ring-shaped complexes | ||
HKNIGPJH_01066 | 1.6e-123 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
HKNIGPJH_01067 | 1.2e-22 | lacY | P | LacY proton/sugar symporter | ||
HKNIGPJH_01068 | 5.1e-147 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_01069 | 3.6e-140 | 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 | ||
HKNIGPJH_01070 | 8.6e-125 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
HKNIGPJH_01071 | 4.5e-157 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
HKNIGPJH_01072 | 5.5e-53 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
HKNIGPJH_01073 | 7.3e-74 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
HKNIGPJH_01074 | 8e-147 | |||||
HKNIGPJH_01075 | 7.1e-186 | sufB | O | FeS assembly protein SufB | ||
HKNIGPJH_01076 | 5.1e-130 | sufD | O | FeS assembly protein SufD | ||
HKNIGPJH_01077 | 1.7e-194 | pknL | 2.7.11.1 | KLT | PASTA | |
HKNIGPJH_01078 | 1.2e-120 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
HKNIGPJH_01079 | 9.2e-124 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HKNIGPJH_01080 | 3.6e-67 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HKNIGPJH_01081 | 8.7e-58 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_01084 | 4e-195 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
HKNIGPJH_01085 | 7.8e-302 | pepD | E | Peptidase family C69 | ||
HKNIGPJH_01088 | 6e-38 | nrdH | O | Glutaredoxin | ||
HKNIGPJH_01089 | 2e-225 | S | Putative ABC-transporter type IV | |||
HKNIGPJH_01090 | 0.0 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_01091 | 2.6e-22 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_01092 | 1.5e-31 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_01093 | 1.7e-56 | htpX | O | Belongs to the peptidase M48B family | ||
HKNIGPJH_01094 | 6.5e-207 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
HKNIGPJH_01095 | 4.1e-86 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HKNIGPJH_01096 | 6.4e-221 | clcA | P | Voltage gated chloride channel | ||
HKNIGPJH_01097 | 2e-129 | 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 | |
HKNIGPJH_01098 | 3.6e-67 | rsfS | 2.7.7.18 | 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 | |
HKNIGPJH_01099 | 4.3e-143 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
HKNIGPJH_01100 | 1.9e-37 | murB | 1.3.1.98 | M | Cell wall formation | |
HKNIGPJH_01101 | 4.8e-266 | E | aromatic amino acid transport protein AroP K03293 | |||
HKNIGPJH_01102 | 6e-123 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
HKNIGPJH_01103 | 1.1e-74 | S | GtrA-like protein | |||
HKNIGPJH_01104 | 3.7e-10 | S | LPXTG-motif cell wall anchor domain protein | |||
HKNIGPJH_01105 | 1.4e-46 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
HKNIGPJH_01106 | 8.8e-223 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
HKNIGPJH_01107 | 1e-37 | 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) | |
HKNIGPJH_01108 | 4e-94 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
HKNIGPJH_01109 | 9e-70 | htpX | O | Belongs to the peptidase M48B family | ||
HKNIGPJH_01110 | 1.3e-124 | KT | MT-A70 | |||
HKNIGPJH_01111 | 5.2e-108 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
HKNIGPJH_01112 | 9.8e-213 | rhaR1 | K | helix_turn_helix, arabinose operon control protein | ||
HKNIGPJH_01113 | 9e-110 | znuC | P | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_01114 | 3.9e-140 | znuB | U | ABC 3 transport family | ||
HKNIGPJH_01115 | 6.1e-58 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
HKNIGPJH_01116 | 1.2e-235 | S | AI-2E family transporter | |||
HKNIGPJH_01118 | 1.2e-61 | 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 | ||
HKNIGPJH_01119 | 3.3e-80 | 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 | ||
HKNIGPJH_01120 | 1.3e-47 | 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 | ||
HKNIGPJH_01121 | 1.9e-145 | K | helix_turn _helix lactose operon repressor | |||
HKNIGPJH_01122 | 1.7e-161 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
HKNIGPJH_01123 | 9.6e-166 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
HKNIGPJH_01124 | 4.5e-98 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
HKNIGPJH_01125 | 3.1e-124 | S | Phospholipase/Carboxylesterase | |||
HKNIGPJH_01126 | 1.1e-124 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
HKNIGPJH_01127 | 1.4e-113 | S | Protein of unknown function DUF262 | |||
HKNIGPJH_01128 | 5.1e-243 | T | Histidine kinase | |||
HKNIGPJH_01129 | 2.6e-40 | V | ABC-2 family transporter protein | |||
HKNIGPJH_01130 | 1.7e-190 | V | ATPases associated with a variety of cellular activities | |||
HKNIGPJH_01131 | 1.9e-56 | T | Histidine kinase | |||
HKNIGPJH_01132 | 2e-103 | 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 | ||
HKNIGPJH_01133 | 2.2e-113 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HKNIGPJH_01134 | 1.8e-34 | pbuX | F | Permease family | ||
HKNIGPJH_01135 | 2.8e-301 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
HKNIGPJH_01136 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
HKNIGPJH_01137 | 3.4e-91 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
HKNIGPJH_01138 | 9.4e-98 | mntP | P | Probably functions as a manganese efflux pump | ||
HKNIGPJH_01139 | 4.9e-134 | |||||
HKNIGPJH_01140 | 4.9e-134 | KT | Transcriptional regulatory protein, C terminal | |||
HKNIGPJH_01141 | 3.2e-123 | 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 | |
HKNIGPJH_01142 | 7.8e-288 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
HKNIGPJH_01143 | 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 | |
HKNIGPJH_01144 | 4.3e-183 | G | Bacterial Ig-like domain (group 4) | |||
HKNIGPJH_01145 | 6.5e-46 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HKNIGPJH_01146 | 3.9e-139 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
HKNIGPJH_01147 | 1.6e-46 | 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 | |
HKNIGPJH_01148 | 2e-115 | S | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_01149 | 2e-13 | |||||
HKNIGPJH_01152 | 4.2e-95 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
HKNIGPJH_01153 | 1.3e-108 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
HKNIGPJH_01154 | 7.2e-11 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
HKNIGPJH_01155 | 4e-131 | ftsK | D | FtsK SpoIIIE family protein | ||
HKNIGPJH_01156 | 1.2e-241 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HKNIGPJH_01157 | 8.5e-77 | S | LytR cell envelope-related transcriptional attenuator | |||
HKNIGPJH_01158 | 1e-79 | 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 | |
HKNIGPJH_01159 | 9.2e-130 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HKNIGPJH_01160 | 8.9e-13 | S | zinc-ribbon domain | |||
HKNIGPJH_01161 | 2.7e-116 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HKNIGPJH_01162 | 2.2e-28 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
HKNIGPJH_01163 | 1.8e-43 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
HKNIGPJH_01165 | 2.3e-84 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
HKNIGPJH_01166 | 5.3e-231 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
HKNIGPJH_01167 | 1.3e-270 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_01168 | 4.8e-37 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
HKNIGPJH_01169 | 5.4e-119 | L | DNA helicase | |||
HKNIGPJH_01170 | 8.8e-150 | L | DNA helicase | |||
HKNIGPJH_01171 | 1.4e-48 | |||||
HKNIGPJH_01172 | 6.1e-252 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
HKNIGPJH_01173 | 1.9e-26 | P | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_01174 | 3.1e-97 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HKNIGPJH_01175 | 5.6e-124 | livF | E | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_01176 | 2.4e-68 | livG | E | ABC transporter | ||
HKNIGPJH_01177 | 4.6e-91 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
HKNIGPJH_01178 | 1.9e-203 | G | Major Facilitator Superfamily | |||
HKNIGPJH_01179 | 9.8e-25 | helY | L | DEAD DEAH box helicase | ||
HKNIGPJH_01180 | 3.5e-79 | helY | L | DEAD DEAH box helicase | ||
HKNIGPJH_01181 | 1e-31 | helY | L | DEAD DEAH box helicase | ||
HKNIGPJH_01182 | 3.3e-49 | D | nuclear chromosome segregation | |||
HKNIGPJH_01183 | 3.4e-126 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
HKNIGPJH_01184 | 1.6e-149 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
HKNIGPJH_01185 | 1.4e-184 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
HKNIGPJH_01186 | 2.7e-296 | yegQ | O | Peptidase family U32 C-terminal domain | ||
HKNIGPJH_01187 | 9.7e-171 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
HKNIGPJH_01188 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
HKNIGPJH_01189 | 1.7e-91 | lemA | S | LemA family | ||
HKNIGPJH_01190 | 1.3e-09 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
HKNIGPJH_01191 | 5.1e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HKNIGPJH_01192 | 8.2e-145 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
HKNIGPJH_01193 | 1.1e-17 | argE | E | Peptidase dimerisation domain | ||
HKNIGPJH_01194 | 3.6e-93 | S | Protein of unknown function (DUF3043) | |||
HKNIGPJH_01195 | 8e-53 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HKNIGPJH_01196 | 6.6e-145 | G | Binding-protein-dependent transport system inner membrane component | |||
HKNIGPJH_01197 | 4.5e-91 | G | PFAM binding-protein-dependent transport systems inner membrane component | |||
HKNIGPJH_01198 | 1.6e-163 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HKNIGPJH_01199 | 1.6e-96 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
HKNIGPJH_01200 | 1.5e-149 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
HKNIGPJH_01201 | 1.4e-240 | trkB | P | Cation transport protein | ||
HKNIGPJH_01203 | 4.4e-183 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
HKNIGPJH_01204 | 7e-77 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
HKNIGPJH_01205 | 1.1e-264 | E | ABC transporter, substrate-binding protein, family 5 | |||
HKNIGPJH_01206 | 5.8e-111 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
HKNIGPJH_01207 | 1.6e-155 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01208 | 1.4e-18 | E | ABC transporter, substrate-binding protein, family 5 | |||
HKNIGPJH_01209 | 8.8e-139 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
HKNIGPJH_01210 | 6.2e-40 | ybdD | S | Selenoprotein, putative | ||
HKNIGPJH_01211 | 1.2e-86 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
HKNIGPJH_01212 | 3.6e-70 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
HKNIGPJH_01213 | 3.4e-129 | KT | Transcriptional regulatory protein, C terminal | |||
HKNIGPJH_01214 | 3e-196 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
HKNIGPJH_01215 | 1.3e-163 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HKNIGPJH_01216 | 3.1e-168 | pstA | P | Phosphate transport system permease | ||
HKNIGPJH_01217 | 3.6e-148 | 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 | |
HKNIGPJH_01218 | 3.1e-143 | P | Zinc-uptake complex component A periplasmic | |||
HKNIGPJH_01219 | 1.1e-237 | pbuO | S | Permease family | ||
HKNIGPJH_01220 | 1.1e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HKNIGPJH_01221 | 1.2e-97 | I | Diacylglycerol kinase catalytic domain | |||
HKNIGPJH_01222 | 2.8e-157 | arbG | K | CAT RNA binding domain | ||
HKNIGPJH_01223 | 4.4e-36 | crr | G | pts system, glucose-specific IIABC component | ||
HKNIGPJH_01224 | 4.5e-163 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
HKNIGPJH_01225 | 2e-104 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
HKNIGPJH_01226 | 3.4e-163 | gltX | 6.1.1.17 | 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) | |
HKNIGPJH_01229 | 1.9e-65 | 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 | ||
HKNIGPJH_01230 | 3.3e-62 | 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 | ||
HKNIGPJH_01231 | 8.4e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HKNIGPJH_01232 | 1.6e-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 | ||
HKNIGPJH_01233 | 2.5e-98 | 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 | |
HKNIGPJH_01234 | 9.9e-239 | 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 | ||
HKNIGPJH_01235 | 9.8e-74 | rplO | J | binds to the 23S rRNA | ||
HKNIGPJH_01236 | 3.4e-25 | rpmD | J | Ribosomal protein L30p/L7e | ||
HKNIGPJH_01237 | 1.2e-92 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HKNIGPJH_01238 | 3.3e-59 | 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 | ||
HKNIGPJH_01239 | 3.8e-96 | 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 | ||
HKNIGPJH_01240 | 4.6e-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 | ||
HKNIGPJH_01241 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HKNIGPJH_01242 | 7.5e-103 | 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 | ||
HKNIGPJH_01243 | 8.7e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HKNIGPJH_01244 | 3e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HKNIGPJH_01245 | 4.9e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HKNIGPJH_01246 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HKNIGPJH_01247 | 1.6e-44 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HKNIGPJH_01248 | 2.8e-51 | L | Restriction endonuclease BglII | |||
HKNIGPJH_01249 | 1.1e-61 | |||||
HKNIGPJH_01250 | 7.1e-27 | D | FtsK/SpoIIIE family | |||
HKNIGPJH_01255 | 2.5e-25 | L | Phage integrase family | |||
HKNIGPJH_01256 | 1.4e-59 | L | Phage integrase family | |||
HKNIGPJH_01258 | 3.8e-187 | K | Helix-turn-helix XRE-family like proteins | |||
HKNIGPJH_01259 | 1.8e-170 | yddG | EG | EamA-like transporter family | ||
HKNIGPJH_01260 | 1.8e-113 | pip | S | YhgE Pip domain protein | ||
HKNIGPJH_01261 | 2e-228 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
HKNIGPJH_01262 | 9e-26 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
HKNIGPJH_01263 | 7.2e-189 | K | Bacterial regulatory proteins, lacI family | |||
HKNIGPJH_01264 | 2.6e-208 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
HKNIGPJH_01265 | 2.7e-213 | S | Histidine phosphatase superfamily (branch 2) | |||
HKNIGPJH_01266 | 3.1e-228 | yliE | T | Putative diguanylate phosphodiesterase | ||
HKNIGPJH_01267 | 5.1e-158 | G | Fructosamine kinase | |||
HKNIGPJH_01268 | 2.5e-88 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
HKNIGPJH_01269 | 4.8e-82 | T | Response regulator receiver domain protein | |||
HKNIGPJH_01270 | 1.6e-229 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
HKNIGPJH_01271 | 1.3e-84 | 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 | |
HKNIGPJH_01272 | 6.9e-168 | relA | 2.7.6.5, 3.1.7.2 | 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 | |
HKNIGPJH_01273 | 9.4e-101 | pdtaR | T | Response regulator receiver domain protein | ||
HKNIGPJH_01274 | 1.6e-171 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
HKNIGPJH_01275 | 5.2e-08 | |||||
HKNIGPJH_01276 | 2.8e-34 | |||||
HKNIGPJH_01277 | 9.3e-89 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
HKNIGPJH_01278 | 9.3e-57 | 3.4.23.43 | S | Type IV leader peptidase family | ||
HKNIGPJH_01279 | 4.3e-89 | 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 | |
HKNIGPJH_01280 | 1.1e-81 | hisA | 3.5.4.19, 3.6.1.31, 5.3.1.16, 5.3.1.24 | E | 1-(5-phosphoribosyl)-5- (5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
HKNIGPJH_01281 | 8.7e-175 | M | LPXTG-motif cell wall anchor domain protein | |||
HKNIGPJH_01282 | 0.0 | oxc | 4.1.1.8 | EH | Thiamine pyrophosphate enzyme, central domain | |
HKNIGPJH_01283 | 3.3e-192 | yfdV | S | Membrane transport protein | ||
HKNIGPJH_01284 | 5e-273 | frc | 2.8.3.16 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HKNIGPJH_01285 | 4.1e-82 | L | Phage integrase family | |||
HKNIGPJH_01286 | 1.4e-70 | 3.2.1.20, 3.5.1.28 | GH31 | V | N-acetylmuramoyl-L-alanine amidase | |
HKNIGPJH_01287 | 1.3e-187 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
HKNIGPJH_01288 | 9.6e-208 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
HKNIGPJH_01289 | 1e-69 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
HKNIGPJH_01290 | 1.7e-227 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HKNIGPJH_01291 | 8.6e-142 | S | Domain of unknown function (DUF4191) | |||
HKNIGPJH_01292 | 1.8e-99 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HKNIGPJH_01293 | 1.8e-181 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
HKNIGPJH_01294 | 2.1e-128 | 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 | |
HKNIGPJH_01295 | 1.2e-65 | 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 | |
HKNIGPJH_01296 | 2.4e-286 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
HKNIGPJH_01297 | 1.6e-162 | G | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_01298 | 8.2e-104 | G | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_01299 | 1.4e-37 | S | G5 | |||
HKNIGPJH_01300 | 1.8e-31 | S | G5 | |||
HKNIGPJH_01302 | 5e-27 | O | Thioredoxin | |||
HKNIGPJH_01303 | 8.8e-109 | J | Acetyltransferase (GNAT) domain | |||
HKNIGPJH_01304 | 8.8e-46 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HKNIGPJH_01305 | 1.1e-95 | bcp | 1.11.1.15 | O | Redoxin | |
HKNIGPJH_01306 | 1.8e-29 | S | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_01307 | 1.1e-256 | relA | 2.7.6.5, 3.1.7.2 | 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 | |
HKNIGPJH_01308 | 1.8e-240 | EGP | Major facilitator Superfamily | |||
HKNIGPJH_01309 | 1.2e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HKNIGPJH_01310 | 2e-269 | KLT | Domain of unknown function (DUF4032) | |||
HKNIGPJH_01311 | 1.6e-210 | ugpC | E | Belongs to the ABC transporter superfamily | ||
HKNIGPJH_01312 | 2.8e-131 | K | LytTr DNA-binding domain | |||
HKNIGPJH_01313 | 2.7e-234 | T | GHKL domain | |||
HKNIGPJH_01314 | 1.1e-30 | |||||
HKNIGPJH_01316 | 2.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HKNIGPJH_01317 | 4.9e-63 | |||||
HKNIGPJH_01319 | 7.5e-101 | XK27_00240 | K | Fic/DOC family | ||
HKNIGPJH_01321 | 1.3e-166 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
HKNIGPJH_01322 | 1.4e-289 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
HKNIGPJH_01323 | 1.7e-70 | rplI | J | Binds to the 23S rRNA | ||
HKNIGPJH_01324 | 3.5e-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 | ||
HKNIGPJH_01325 | 9.7e-70 | ssb1 | L | Single-stranded DNA-binding protein | ||
HKNIGPJH_01326 | 2.5e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HKNIGPJH_01327 | 1.6e-185 | 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) | |
HKNIGPJH_01328 | 5.7e-175 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
HKNIGPJH_01329 | 6.7e-179 | EGP | Major Facilitator Superfamily | |||
HKNIGPJH_01330 | 8.9e-248 | M | domain protein | |||
HKNIGPJH_01331 | 9e-209 | uvrA3 | 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 | ||
HKNIGPJH_01332 | 3.1e-68 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HKNIGPJH_01333 | 3.7e-182 | adh3 | C | Zinc-binding dehydrogenase | ||
HKNIGPJH_01334 | 1.4e-148 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HKNIGPJH_01335 | 8.2e-218 | 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 | |
HKNIGPJH_01336 | 3.6e-304 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HKNIGPJH_01337 | 6.8e-133 | KT | Response regulator receiver domain protein | |||
HKNIGPJH_01338 | 1.3e-27 | |||||
HKNIGPJH_01339 | 5.5e-53 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
HKNIGPJH_01340 | 2.8e-42 | azlC | E | AzlC protein | ||
HKNIGPJH_01341 | 8.3e-50 | 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 | |
HKNIGPJH_01342 | 2.6e-114 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
HKNIGPJH_01343 | 1.1e-38 | csoR | S | Metal-sensitive transcriptional repressor | ||
HKNIGPJH_01344 | 1.9e-77 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HKNIGPJH_01345 | 4.4e-50 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
HKNIGPJH_01346 | 4.5e-26 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
HKNIGPJH_01347 | 7.9e-43 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
HKNIGPJH_01348 | 5.3e-119 | ykoE | S | ABC-type cobalt transport system, permease component | ||
HKNIGPJH_01349 | 1.3e-31 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HKNIGPJH_01350 | 2.1e-114 | lipA | I | Hydrolase, alpha beta domain protein | ||
HKNIGPJH_01351 | 5e-27 | S | Psort location Cytoplasmic, score 8.87 | |||
HKNIGPJH_01352 | 1.7e-113 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HKNIGPJH_01353 | 4.6e-120 | 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 | ||
HKNIGPJH_01355 | 3.6e-117 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
HKNIGPJH_01356 | 6.4e-104 | G | Bacterial Ig-like domain (group 4) | |||
HKNIGPJH_01357 | 8.7e-40 | G | Bacterial Ig-like domain (group 4) | |||
HKNIGPJH_01358 | 0.0 | sca1 | 3.2.1.187 | GH121 | DG | Bacterial Ig-like domain (group 4) |
HKNIGPJH_01359 | 2.2e-125 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
HKNIGPJH_01360 | 1.3e-229 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
HKNIGPJH_01361 | 3.2e-24 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
HKNIGPJH_01362 | 5.6e-129 | pgm3 | G | Phosphoglycerate mutase family | ||
HKNIGPJH_01363 | 3.4e-51 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
HKNIGPJH_01364 | 9e-184 | lacR | K | Transcriptional regulator, LacI family | ||
HKNIGPJH_01365 | 6.5e-31 | bioY | S | BioY family | ||
HKNIGPJH_01366 | 1.8e-187 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
HKNIGPJH_01367 | 8e-64 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
HKNIGPJH_01368 | 5.7e-85 | K | Cro/C1-type HTH DNA-binding domain | |||
HKNIGPJH_01369 | 3.2e-54 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HKNIGPJH_01370 | 4.8e-93 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
HKNIGPJH_01371 | 4.2e-264 | gatA | 6.3.5.6, 6.3.5.7 | F | 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) | |
HKNIGPJH_01373 | 1.3e-199 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HKNIGPJH_01374 | 5.8e-32 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
HKNIGPJH_01375 | 7.4e-166 | 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 | |
HKNIGPJH_01376 | 3.6e-41 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
HKNIGPJH_01377 | 2e-90 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
HKNIGPJH_01378 | 4.1e-112 | S | domain protein | |||
HKNIGPJH_01379 | 1e-221 | S | Zincin-like metallopeptidase | |||
HKNIGPJH_01380 | 9.6e-225 | 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) | |
HKNIGPJH_01381 | 1.1e-11 | 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) | |
HKNIGPJH_01382 | 8.5e-84 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HKNIGPJH_01383 | 1.4e-150 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
HKNIGPJH_01384 | 7.7e-169 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
HKNIGPJH_01385 | 2.2e-159 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HKNIGPJH_01386 | 4.4e-123 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_01387 | 4e-190 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HKNIGPJH_01388 | 5.2e-46 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HKNIGPJH_01389 | 1.5e-169 | cotH | M | CotH kinase protein | ||
HKNIGPJH_01390 | 1.3e-143 | S | Sulfite exporter TauE/SafE | |||
HKNIGPJH_01391 | 3.9e-93 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HKNIGPJH_01392 | 1.8e-56 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HKNIGPJH_01393 | 3.2e-101 | |||||
HKNIGPJH_01394 | 1e-60 | 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 | |
HKNIGPJH_01395 | 1.2e-186 | G | Major Facilitator Superfamily | |||
HKNIGPJH_01396 | 2.2e-128 | 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 | ||
HKNIGPJH_01397 | 1.5e-139 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01398 | 3.2e-92 | V | ABC-2 family transporter protein | |||
HKNIGPJH_01399 | 2.8e-143 | V | ABC-2 family transporter protein | |||
HKNIGPJH_01400 | 3.3e-40 | G | Transporter major facilitator family protein | |||
HKNIGPJH_01401 | 3.8e-10 | bioY | S | BioY family | ||
HKNIGPJH_01402 | 3.9e-162 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
HKNIGPJH_01403 | 3.5e-35 | |||||
HKNIGPJH_01404 | 1.8e-61 | yebC | K | transcriptional regulatory protein | ||
HKNIGPJH_01405 | 5.1e-99 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
HKNIGPJH_01406 | 1.1e-203 | trpE | 4.1.3.27 | E | 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 | |
HKNIGPJH_01407 | 5.2e-75 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HKNIGPJH_01408 | 9.1e-14 | S | Psort location Extracellular, score 8.82 | |||
HKNIGPJH_01409 | 2.8e-210 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
HKNIGPJH_01410 | 1.5e-84 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
HKNIGPJH_01411 | 1.7e-41 | XAC3035 | O | Glutaredoxin | ||
HKNIGPJH_01412 | 2.7e-20 | P | Belongs to the ABC transporter superfamily | |||
HKNIGPJH_01413 | 1.7e-73 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
HKNIGPJH_01414 | 1.4e-142 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HKNIGPJH_01415 | 1e-27 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
HKNIGPJH_01416 | 4.2e-186 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
HKNIGPJH_01417 | 1.9e-219 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
HKNIGPJH_01418 | 1.3e-171 | whiA | K | May be required for sporulation | ||
HKNIGPJH_01419 | 2.6e-17 | yxiO | S | Vacuole effluxer Atg22 like | ||
HKNIGPJH_01420 | 6.1e-39 | yxiO | S | Vacuole effluxer Atg22 like | ||
HKNIGPJH_01421 | 6.5e-41 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HKNIGPJH_01422 | 8.2e-34 | |||||
HKNIGPJH_01423 | 3e-131 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HKNIGPJH_01424 | 3.5e-103 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
HKNIGPJH_01425 | 5.3e-192 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
HKNIGPJH_01426 | 2.1e-188 | yegU | O | ADP-ribosylglycohydrolase | ||
HKNIGPJH_01427 | 8.3e-190 | yegV | G | pfkB family carbohydrate kinase | ||
HKNIGPJH_01428 | 1.1e-270 | U | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
HKNIGPJH_01429 | 1.5e-103 | Q | Isochorismatase family | |||
HKNIGPJH_01430 | 2.3e-214 | S | Choline/ethanolamine kinase | |||
HKNIGPJH_01431 | 5.6e-275 | eat | E | Amino acid permease | ||
HKNIGPJH_01432 | 1.2e-108 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
HKNIGPJH_01433 | 1.7e-108 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HKNIGPJH_01434 | 2.6e-115 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
HKNIGPJH_01435 | 3.2e-56 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HKNIGPJH_01436 | 9e-18 | |||||
HKNIGPJH_01437 | 3e-54 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HKNIGPJH_01438 | 3.6e-28 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HKNIGPJH_01439 | 4.5e-195 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
HKNIGPJH_01440 | 1.3e-34 | aspT | EK | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
HKNIGPJH_01441 | 1.4e-82 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HKNIGPJH_01442 | 1.2e-83 | P | Cobalt transport protein | |||
HKNIGPJH_01443 | 2.6e-80 | terC | P | Integral membrane protein, TerC family | ||
HKNIGPJH_01444 | 4.8e-128 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
HKNIGPJH_01445 | 2.5e-115 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
HKNIGPJH_01446 | 1.7e-134 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
HKNIGPJH_01447 | 3e-167 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
HKNIGPJH_01448 | 3.1e-33 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
HKNIGPJH_01449 | 3.3e-33 | K | helix_turn_helix, Lux Regulon | |||
HKNIGPJH_01450 | 8.2e-160 | T | Histidine kinase | |||
HKNIGPJH_01451 | 9.9e-55 | |||||
HKNIGPJH_01452 | 1.4e-35 | 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 | ||
HKNIGPJH_01453 | 3.6e-201 | K | Cell envelope-related transcriptional attenuator domain | |||
HKNIGPJH_01454 | 1.4e-66 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_01455 | 8.3e-35 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
HKNIGPJH_01456 | 3.7e-23 | M | Protein of unknown function (DUF3737) | |||
HKNIGPJH_01457 | 1.8e-81 | 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 | ||
HKNIGPJH_01458 | 2.1e-66 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
HKNIGPJH_01459 | 1.4e-153 | E | ABC transporter, substrate-binding protein, family 5 | |||
HKNIGPJH_01460 | 1.4e-47 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
HKNIGPJH_01461 | 5.4e-35 | S | Transmembrane domain of unknown function (DUF3566) | |||
HKNIGPJH_01462 | 4.4e-88 | zur | P | Belongs to the Fur family | ||
HKNIGPJH_01463 | 3.1e-80 | 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) | |
HKNIGPJH_01464 | 2.8e-140 | rmuC | S | RmuC family | ||
HKNIGPJH_01465 | 1e-154 | lon | T | Belongs to the peptidase S16 family | ||
HKNIGPJH_01466 | 4.7e-96 | G | Bacterial extracellular solute-binding protein | |||
HKNIGPJH_01467 | 2.2e-215 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
HKNIGPJH_01468 | 3e-46 | S | Protein of unknown function (DUF3046) | |||
HKNIGPJH_01469 | 6.1e-80 | K | Helix-turn-helix XRE-family like proteins | |||
HKNIGPJH_01470 | 7.4e-76 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
HKNIGPJH_01471 | 4.5e-92 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
HKNIGPJH_01472 | 4.8e-230 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01473 | 1e-162 | malG | G | Binding-protein-dependent transport system inner membrane component | ||
HKNIGPJH_01474 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HKNIGPJH_01475 | 5.4e-144 | S | HAD-hyrolase-like | |||
HKNIGPJH_01476 | 2e-141 | traX | S | TraX protein | ||
HKNIGPJH_01477 | 1.3e-193 | K | Psort location Cytoplasmic, score | |||
HKNIGPJH_01478 | 7.6e-174 | pelF | GT4 | M | Domain of unknown function (DUF3492) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)