ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HNJLMKBB_00001 | 1.1e-167 | S | dextransucrase activity | |||
HNJLMKBB_00002 | 8.5e-75 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
HNJLMKBB_00003 | 4.8e-102 | S | Psort location CytoplasmicMembrane, score | |||
HNJLMKBB_00004 | 2.4e-51 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
HNJLMKBB_00005 | 2.6e-17 | S | Accessory secretory protein Sec Asp4 | |||
HNJLMKBB_00006 | 3.6e-16 | S | Accessory secretory protein Sec, Asp5 | |||
HNJLMKBB_00007 | 8.2e-126 | V | ABC transporter (Permease | |||
HNJLMKBB_00008 | 6.1e-67 | proWX | P | ABC transporter | ||
HNJLMKBB_00009 | 2.3e-117 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HNJLMKBB_00010 | 6.9e-197 | yceA | S | Belongs to the UPF0176 family | ||
HNJLMKBB_00011 | 2.1e-160 | oppF | P | Belongs to the ABC transporter superfamily | ||
HNJLMKBB_00012 | 1.2e-184 | ydcQ | D | Ftsk spoiiie family protein | ||
HNJLMKBB_00013 | 8.4e-201 | S | Protein of unknown function (DUF3114) | |||
HNJLMKBB_00014 | 2.6e-09 | sraP | UW | domain, Protein | ||
HNJLMKBB_00015 | 3.9e-167 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
HNJLMKBB_00016 | 2.5e-115 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HNJLMKBB_00017 | 1.7e-125 | vicK | 2.7.13.3 | T | Histidine kinase | |
HNJLMKBB_00018 | 6.8e-108 | rbn | E | Belongs to the UPF0761 family | ||
HNJLMKBB_00019 | 3.2e-142 | sbcC | L | ATPase involved in DNA repair | ||
HNJLMKBB_00020 | 2.3e-198 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
HNJLMKBB_00021 | 3.6e-49 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
HNJLMKBB_00022 | 6.3e-114 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
HNJLMKBB_00023 | 4.3e-84 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
HNJLMKBB_00024 | 1.1e-294 | yfmM | S | abc transporter atp-binding protein | ||
HNJLMKBB_00025 | 1.4e-256 | noxE | P | NADH oxidase | ||
HNJLMKBB_00026 | 4.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HNJLMKBB_00027 | 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 | |
HNJLMKBB_00028 | 7.9e-132 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
HNJLMKBB_00029 | 2.8e-182 | 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 | ||
HNJLMKBB_00030 | 1.5e-86 | E | Alpha beta hydrolase | |||
HNJLMKBB_00031 | 2.3e-69 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
HNJLMKBB_00032 | 6.6e-173 | 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 | |
HNJLMKBB_00033 | 7e-46 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
HNJLMKBB_00034 | 7.1e-46 | ahpF | O | alkyl hydroperoxide reductase | ||
HNJLMKBB_00036 | 1.2e-94 | S | reductase | |||
HNJLMKBB_00037 | 2.1e-76 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
HNJLMKBB_00038 | 2.7e-31 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
HNJLMKBB_00039 | 2.9e-142 | cvfB | S | Protein conserved in bacteria | ||
HNJLMKBB_00040 | 3.7e-34 | yozE | S | Belongs to the UPF0346 family | ||
HNJLMKBB_00041 | 2.8e-213 | XK27_08635 | S | UPF0210 protein | ||
HNJLMKBB_00042 | 1.3e-54 | whiA | K | May be required for sporulation | ||
HNJLMKBB_00043 | 1.2e-82 | cjaA | ET | ABC transporter substrate-binding protein | ||
HNJLMKBB_00045 | 1.9e-84 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
HNJLMKBB_00046 | 2.9e-94 | vanY | 3.4.17.14, 3.5.1.28 | M | D-alanyl-D-alanine carboxypeptidase | |
HNJLMKBB_00047 | 6.7e-59 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
HNJLMKBB_00048 | 9.6e-138 | hisF | 3.5.4.19, 3.6.1.31 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
HNJLMKBB_00049 | 1.2e-53 | T | Ser Thr phosphatase family protein | |||
HNJLMKBB_00050 | 2.7e-72 | M | Putative cell wall binding repeat | |||
HNJLMKBB_00052 | 1.7e-36 | spiA | K | sequence-specific DNA binding | ||
HNJLMKBB_00053 | 2.4e-167 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNJLMKBB_00054 | 1.4e-44 | ylbM | S | Belongs to the UPF0348 family | ||
HNJLMKBB_00055 | 7.8e-39 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
HNJLMKBB_00056 | 1.6e-44 | yoeB | S | Addiction module toxin, Txe YoeB family | ||
HNJLMKBB_00057 | 2.2e-134 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNJLMKBB_00058 | 9.3e-59 | P | ABC transporter (Permease | |||
HNJLMKBB_00059 | 8.7e-168 | pbuX | F | xanthine permease | ||
HNJLMKBB_00060 | 3.8e-102 | kcsA | P | Ion transport protein | ||
HNJLMKBB_00061 | 5.8e-103 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HNJLMKBB_00063 | 2e-214 | 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 | ||
HNJLMKBB_00065 | 5.5e-193 | yjbB | G | Permeases of the major facilitator superfamily | ||
HNJLMKBB_00066 | 8.2e-61 | S | von Willebrand factor (vWF) type A domain | |||
HNJLMKBB_00067 | 1.5e-33 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
HNJLMKBB_00068 | 5.5e-14 | S | Domain of unknown function (DUF4767) | |||
HNJLMKBB_00069 | 4.5e-13 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
HNJLMKBB_00070 | 3.2e-13 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
HNJLMKBB_00071 | 1.1e-64 | S | CAAX protease self-immunity | |||
HNJLMKBB_00072 | 2.2e-111 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
HNJLMKBB_00073 | 7e-158 | 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 | |
HNJLMKBB_00074 | 2.6e-121 | scrA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNJLMKBB_00075 | 1.8e-75 | ctsR | K | Belongs to the CtsR family | ||
HNJLMKBB_00076 | 2.3e-173 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HNJLMKBB_00077 | 7.9e-89 | |||||
HNJLMKBB_00078 | 4.3e-33 | |||||
HNJLMKBB_00079 | 1.1e-56 | I | acyl-CoA dehydrogenase | |||
HNJLMKBB_00080 | 4.9e-187 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HNJLMKBB_00081 | 4.7e-138 | yeiH | S | Membrane | ||
HNJLMKBB_00082 | 4.8e-53 | 3.4.21.110 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
HNJLMKBB_00083 | 6.7e-80 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNJLMKBB_00084 | 5.5e-18 | sufB | O | assembly protein SufB | ||
HNJLMKBB_00085 | 2.2e-35 | adcB | P | ABC transporter (Permease | ||
HNJLMKBB_00086 | 9.2e-116 | 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 | ||
HNJLMKBB_00087 | 8.6e-57 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
HNJLMKBB_00088 | 1.9e-144 | ylmH | S | conserved protein, contains S4-like domain | ||
HNJLMKBB_00089 | 2.9e-30 | yggT | D | integral membrane protein | ||
HNJLMKBB_00090 | 2.2e-86 | sepF | D | cell septum assembly | ||
HNJLMKBB_00091 | 2.3e-122 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
HNJLMKBB_00092 | 4.7e-233 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
HNJLMKBB_00093 | 7.1e-224 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
HNJLMKBB_00094 | 3.8e-130 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HNJLMKBB_00095 | 2.8e-199 | murG | 2.4.1.227 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
HNJLMKBB_00096 | 2.8e-85 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HNJLMKBB_00097 | 1.6e-208 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
HNJLMKBB_00098 | 5.3e-110 | msmX | P | Belongs to the ABC transporter superfamily | ||
HNJLMKBB_00099 | 1.9e-151 | tcdB | S | dextransucrase activity | ||
HNJLMKBB_00100 | 2.8e-114 | fliF | 2.1.1.72 | N | bacterial-type flagellum-dependent cell motility | |
HNJLMKBB_00101 | 1.1e-34 | yhaI | L | Membrane | ||
HNJLMKBB_00102 | 8e-135 | S | Domain of unknown function (DUF4173) | |||
HNJLMKBB_00103 | 3.5e-71 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
HNJLMKBB_00104 | 1.4e-61 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
HNJLMKBB_00105 | 7.9e-140 | deoD_1 | 2.4.2.3 | F | Phosphorylase superfamily | |
HNJLMKBB_00106 | 1.4e-100 | malL_2 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein |
HNJLMKBB_00107 | 1.1e-30 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | PTS system maltose-specific EIICB component | |
HNJLMKBB_00108 | 3.5e-194 | zmpB | M | signal peptide protein, YSIRK family | ||
HNJLMKBB_00109 | 3.4e-121 | 1.6.5.2 | GM | epimerase | ||
HNJLMKBB_00110 | 1.8e-20 | dinF | V | Mate efflux family protein | ||
HNJLMKBB_00112 | 2.5e-95 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HNJLMKBB_00113 | 1.7e-182 | galR | K | Transcriptional regulator | ||
HNJLMKBB_00114 | 1.9e-81 | XK27_05505 | S | Psort location CytoplasmicMembrane, score | ||
HNJLMKBB_00116 | 2.5e-58 | estA | CE1 | S | Esterase | |
HNJLMKBB_00117 | 6.6e-105 | mdlB | V | abc transporter atp-binding protein | ||
HNJLMKBB_00118 | 7.6e-180 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
HNJLMKBB_00119 | 2.7e-171 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
HNJLMKBB_00120 | 8.2e-66 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
HNJLMKBB_00121 | 1.4e-116 | cppA | E | CppA N-terminal | ||
HNJLMKBB_00122 | 5.9e-95 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
HNJLMKBB_00123 | 1.5e-49 | XK27_09825 | V | abc transporter atp-binding protein | ||
HNJLMKBB_00124 | 1.2e-180 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HNJLMKBB_00125 | 3.6e-155 | L | Transposase IS116 IS110 IS902 | |||
HNJLMKBB_00126 | 2.9e-79 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
HNJLMKBB_00127 | 6.7e-179 | ftsW | D | Belongs to the SEDS family | ||
HNJLMKBB_00128 | 1.5e-152 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
HNJLMKBB_00131 | 6.6e-59 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
HNJLMKBB_00132 | 2.1e-88 | 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 | |
HNJLMKBB_00133 | 5.7e-22 | V | ABC transporter | |||
HNJLMKBB_00134 | 6.1e-126 | yeeN | K | transcriptional regulatory protein | ||
HNJLMKBB_00135 | 2e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HNJLMKBB_00136 | 4.6e-29 | yhaI | S | Protein of unknown function (DUF805) | ||
HNJLMKBB_00137 | 5.3e-95 | K | helix_turn_helix, Lux Regulon | |||
HNJLMKBB_00138 | 3.6e-58 | ebsA | S | Family of unknown function (DUF5322) | ||
HNJLMKBB_00139 | 2.7e-114 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
HNJLMKBB_00140 | 1.4e-59 | XK27_04120 | S | Putative amino acid metabolism | ||
HNJLMKBB_00141 | 1.1e-60 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNJLMKBB_00142 | 2.7e-183 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
HNJLMKBB_00143 | 1.6e-140 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HNJLMKBB_00144 | 1.1e-217 | araT | 2.6.1.1 | E | Aminotransferase | |
HNJLMKBB_00145 | 9.5e-175 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
HNJLMKBB_00146 | 4.1e-84 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
HNJLMKBB_00147 | 1.8e-82 | mreD | M | rod shape-determining protein MreD | ||
HNJLMKBB_00148 | 1.9e-107 | mreC | M | Involved in formation and maintenance of cell shape | ||
HNJLMKBB_00153 | 6.5e-78 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HNJLMKBB_00154 | 2.6e-114 | fecD | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
HNJLMKBB_00155 | 1.9e-47 | adcR | K | transcriptional | ||
HNJLMKBB_00156 | 8.3e-22 | clpE | O | Belongs to the ClpA ClpB family | ||
HNJLMKBB_00157 | 6.1e-79 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
HNJLMKBB_00159 | 2.6e-97 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
HNJLMKBB_00160 | 2e-107 | V | CAAX protease self-immunity | |||
HNJLMKBB_00161 | 8.8e-27 | lanR | K | sequence-specific DNA binding | ||
HNJLMKBB_00162 | 2.6e-109 | fasA | KT | Response regulator of the LytR AlgR family | ||
HNJLMKBB_00163 | 1.2e-99 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
HNJLMKBB_00164 | 7.7e-110 | cps4C | M | biosynthesis protein | ||
HNJLMKBB_00165 | 6.3e-44 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
HNJLMKBB_00166 | 6.4e-62 | XK27_05710 | K | Acetyltransferase (GNAT) domain | ||
HNJLMKBB_00167 | 2.3e-82 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
HNJLMKBB_00168 | 5.4e-124 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HNJLMKBB_00169 | 7.5e-84 | S | Domain of unknown function DUF87 | |||
HNJLMKBB_00170 | 1.1e-147 | nptA | P | COG1283 Na phosphate symporter | ||
HNJLMKBB_00171 | 1.8e-145 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
HNJLMKBB_00172 | 1.8e-96 | ypmS | S | Protein conserved in bacteria | ||
HNJLMKBB_00173 | 6.3e-39 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
HNJLMKBB_00175 | 3.4e-177 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
HNJLMKBB_00176 | 2.1e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HNJLMKBB_00177 | 4.9e-290 | 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) | |
HNJLMKBB_00178 | 6.6e-190 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
HNJLMKBB_00179 | 3.4e-97 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
HNJLMKBB_00180 | 5.1e-24 | 2.4.1.21 | GT5 | M | Right handed beta helix region | |
HNJLMKBB_00181 | 5.7e-109 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
HNJLMKBB_00182 | 2.7e-109 | XK27_07020 | S | Belongs to the UPF0371 family | ||
HNJLMKBB_00183 | 3e-119 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
HNJLMKBB_00184 | 2.8e-91 | S | Protein of unknown function (DUF3278) | |||
HNJLMKBB_00185 | 1.3e-22 | WQ51_00220 | K | Helix-turn-helix domain | ||
HNJLMKBB_00186 | 1.7e-117 | T | response regulator | |||
HNJLMKBB_00187 | 4.2e-17 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
HNJLMKBB_00188 | 9.8e-158 | 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 | ||
HNJLMKBB_00189 | 2.2e-93 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
HNJLMKBB_00190 | 6.7e-90 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HNJLMKBB_00191 | 3e-47 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
HNJLMKBB_00192 | 1.2e-112 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
HNJLMKBB_00193 | 1.8e-63 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
HNJLMKBB_00194 | 1.2e-191 | tcsA | S | membrane | ||
HNJLMKBB_00195 | 2.4e-281 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
HNJLMKBB_00196 | 1.9e-176 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
HNJLMKBB_00197 | 1.2e-169 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
HNJLMKBB_00198 | 5.8e-120 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
HNJLMKBB_00199 | 4.7e-168 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HNJLMKBB_00200 | 9.5e-124 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
HNJLMKBB_00201 | 5.3e-72 | bdhA | 1.1.1.303, 1.1.1.4 | E | Dehydrogenase | |
HNJLMKBB_00202 | 1.8e-44 | 1.13.11.2 | S | glyoxalase | ||
HNJLMKBB_00203 | 1.5e-109 | XK27_02070 | S | nitroreductase | ||
HNJLMKBB_00204 | 4.9e-12 | comGF | U | Competence protein ComGF | ||
HNJLMKBB_00205 | 2e-12 | comGF | U | Putative Competence protein ComGF | ||
HNJLMKBB_00206 | 1e-108 | lytC | 3.4.17.14, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
HNJLMKBB_00207 | 1e-184 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
HNJLMKBB_00209 | 3.2e-68 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HNJLMKBB_00210 | 1.2e-09 | |||||
HNJLMKBB_00211 | 3.1e-29 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
HNJLMKBB_00212 | 2.6e-26 | L | Transposase | |||
HNJLMKBB_00213 | 1.4e-145 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
HNJLMKBB_00214 | 8.1e-85 | BP1961 | P | oxidoreductase | ||
HNJLMKBB_00215 | 1.2e-32 | BP1961 | P | oxidoreductase | ||
HNJLMKBB_00216 | 1e-14 | XK27_10475 | S | oxidoreductase | ||
HNJLMKBB_00217 | 2.6e-42 | pepV | 3.5.1.18 | E | Dipeptidase | |
HNJLMKBB_00218 | 7.9e-108 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
HNJLMKBB_00219 | 4.5e-55 | cadC | K | Bacterial regulatory protein, arsR family | ||
HNJLMKBB_00220 | 4.4e-101 | cadD | P | cadmium resistance | ||
HNJLMKBB_00222 | 7.3e-59 | ywaF | S | Integral membrane protein (intg_mem_TP0381) | ||
HNJLMKBB_00223 | 1.5e-10 | S | hydrolase | |||
HNJLMKBB_00224 | 7.3e-115 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase | |
HNJLMKBB_00225 | 7.8e-121 | V | ABC transporter (permease) | |||
HNJLMKBB_00226 | 1.5e-57 | lamB | S | LamB/YcsF family | ||
HNJLMKBB_00227 | 1.7e-102 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
HNJLMKBB_00228 | 4.4e-83 | S | dextransucrase activity | |||
HNJLMKBB_00229 | 5.3e-107 | G | Belongs to the phosphoglycerate mutase family | |||
HNJLMKBB_00230 | 1.4e-25 | |||||
HNJLMKBB_00231 | 1.3e-102 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
HNJLMKBB_00232 | 8.4e-262 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
HNJLMKBB_00233 | 8.2e-19 | |||||
HNJLMKBB_00234 | 1.5e-201 | pmrB | EGP | Major facilitator Superfamily | ||
HNJLMKBB_00235 | 2.3e-63 | tdcF | 3.5.99.10 | J | endoribonuclease L-PSP | |
HNJLMKBB_00236 | 1.2e-123 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
HNJLMKBB_00237 | 2.8e-81 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
HNJLMKBB_00238 | 1.2e-134 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
HNJLMKBB_00239 | 1.3e-190 | ymfF | S | Peptidase M16 | ||
HNJLMKBB_00240 | 3.7e-235 | ymfH | S | Peptidase M16 | ||
HNJLMKBB_00241 | 2.8e-130 | S | sequence-specific DNA binding | |||
HNJLMKBB_00242 | 4.1e-90 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HNJLMKBB_00243 | 2.8e-151 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HNJLMKBB_00244 | 4.7e-154 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
HNJLMKBB_00245 | 1.7e-132 | ecfT | P | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HNJLMKBB_00246 | 1.3e-279 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
HNJLMKBB_00247 | 1.3e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HNJLMKBB_00248 | 5.6e-50 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
HNJLMKBB_00249 | 1.4e-68 | ypsA | S | Belongs to the UPF0398 family | ||
HNJLMKBB_00250 | 5.4e-84 | S | membrane | |||
HNJLMKBB_00251 | 3e-96 | P | VTC domain | |||
HNJLMKBB_00252 | 1.3e-222 | cotH | M | CotH kinase protein | ||
HNJLMKBB_00253 | 5.4e-182 | pelG | M | Putative exopolysaccharide Exporter (EPS-E) | ||
HNJLMKBB_00254 | 3.7e-51 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
HNJLMKBB_00255 | 0.0 | plyA3 | 3.2.1.18 | GH33 | M | Parallel beta-helix repeats |
HNJLMKBB_00256 | 5.4e-48 | plyA3 | M | Parallel beta-helix repeats | ||
HNJLMKBB_00257 | 3.1e-37 | plyA3 | 3.2.1.18 | GH33 | M | Parallel beta-helix repeats |
HNJLMKBB_00258 | 8e-213 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
HNJLMKBB_00259 | 2.5e-62 | glnR | K | Transcriptional regulator | ||
HNJLMKBB_00260 | 5.2e-264 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HNJLMKBB_00261 | 4e-113 | pscB | M | CHAP domain protein | ||
HNJLMKBB_00262 | 0.0 | rnjA | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HNJLMKBB_00263 | 1.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
HNJLMKBB_00264 | 3.5e-115 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
HNJLMKBB_00265 | 2e-205 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HNJLMKBB_00266 | 1.4e-189 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HNJLMKBB_00267 | 2.9e-99 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
HNJLMKBB_00268 | 2.5e-294 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HNJLMKBB_00269 | 6e-157 | S | CHAP domain | |||
HNJLMKBB_00270 | 2.6e-33 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HNJLMKBB_00271 | 3.5e-112 | acuB | S | CBS domain | ||
HNJLMKBB_00272 | 5.6e-124 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
HNJLMKBB_00273 | 2.4e-136 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
HNJLMKBB_00274 | 4.9e-139 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
HNJLMKBB_00275 | 4.2e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
HNJLMKBB_00276 | 9.1e-212 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
HNJLMKBB_00277 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
HNJLMKBB_00278 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
HNJLMKBB_00279 | 1.8e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HNJLMKBB_00280 | 2.1e-43 | yrzB | S | Belongs to the UPF0473 family | ||
HNJLMKBB_00281 | 1.9e-295 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
HNJLMKBB_00282 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HNJLMKBB_00283 | 7.5e-14 | |||||
HNJLMKBB_00284 | 1.8e-19 | cbf | S | 3'-5' exoribonuclease yhaM | ||
HNJLMKBB_00285 | 4e-142 | purR | 2.4.2.7 | F | operon repressor | |
HNJLMKBB_00286 | 2.3e-69 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
HNJLMKBB_00287 | 3.9e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
HNJLMKBB_00288 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
HNJLMKBB_00289 | 7.1e-181 | gap | 1.2.1.12 | C | Glyceraldehyde 3-phosphate dehydrogenase, C-terminal domain | |
HNJLMKBB_00290 | 5.1e-306 | ybiT | S | abc transporter atp-binding protein | ||
HNJLMKBB_00291 | 7.8e-152 | yvjA | S | membrane | ||
HNJLMKBB_00292 | 1.2e-191 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
HNJLMKBB_00293 | 5.6e-275 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
HNJLMKBB_00294 | 7e-27 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
HNJLMKBB_00295 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
HNJLMKBB_00296 | 1.1e-200 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
HNJLMKBB_00297 | 3e-223 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
HNJLMKBB_00298 | 1.9e-153 | K | sequence-specific DNA binding | |||
HNJLMKBB_00299 | 2.4e-105 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
HNJLMKBB_00300 | 8.7e-88 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
HNJLMKBB_00301 | 6.1e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HNJLMKBB_00302 | 5.4e-256 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
HNJLMKBB_00303 | 1.5e-71 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
HNJLMKBB_00304 | 5.2e-52 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
HNJLMKBB_00305 | 2.6e-233 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
HNJLMKBB_00306 | 1.8e-125 | IQ | reductase | |||
HNJLMKBB_00307 | 3e-162 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
HNJLMKBB_00308 | 1.4e-90 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
HNJLMKBB_00309 | 1.8e-223 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
HNJLMKBB_00310 | 5.6e-63 | yutD | J | protein conserved in bacteria | ||
HNJLMKBB_00311 | 1.3e-257 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
HNJLMKBB_00313 | 1.3e-27 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
HNJLMKBB_00314 | 5.9e-258 | ykoD | P | abc transporter atp-binding protein | ||
HNJLMKBB_00315 | 1e-148 | cbiQ | P | cobalt transport | ||
HNJLMKBB_00316 | 8e-120 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
HNJLMKBB_00317 | 3.3e-237 | P | COG0168 Trk-type K transport systems, membrane components | |||
HNJLMKBB_00318 | 7.6e-129 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
HNJLMKBB_00319 | 3.9e-72 | badR | K | Transcriptional regulator, marr family | ||
HNJLMKBB_00320 | 1.2e-35 | XK27_02060 | S | Transglycosylase associated protein | ||
HNJLMKBB_00321 | 8.6e-237 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
HNJLMKBB_00322 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HNJLMKBB_00323 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
HNJLMKBB_00324 | 3.2e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HNJLMKBB_00325 | 3.9e-139 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
HNJLMKBB_00326 | 4e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
HNJLMKBB_00327 | 1e-78 | 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 | |
HNJLMKBB_00328 | 8.2e-108 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
HNJLMKBB_00329 | 7.9e-230 | XK27_09615 | C | reductase | ||
HNJLMKBB_00330 | 9e-139 | fnt | P | Formate nitrite transporter | ||
HNJLMKBB_00331 | 6.7e-96 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
HNJLMKBB_00332 | 5.7e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HNJLMKBB_00333 | 2.5e-192 | 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) | ||
HNJLMKBB_00334 | 8.8e-113 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
HNJLMKBB_00335 | 7.9e-46 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
HNJLMKBB_00336 | 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 | ||
HNJLMKBB_00337 | 1.4e-136 | P | cobalt transport protein | |||
HNJLMKBB_00338 | 1.3e-176 | cbiM | P | biosynthesis protein CbiM | ||
HNJLMKBB_00339 | 5.2e-161 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
HNJLMKBB_00340 | 9.5e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
HNJLMKBB_00341 | 5.3e-130 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
HNJLMKBB_00342 | 2.5e-77 | ureE | O | enzyme active site formation | ||
HNJLMKBB_00343 | 2.4e-74 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
HNJLMKBB_00344 | 1.2e-41 | yjdF | S | Protein of unknown function (DUF2992) | ||
HNJLMKBB_00345 | 5.6e-150 | cylA | V | abc transporter atp-binding protein | ||
HNJLMKBB_00346 | 1.9e-131 | cylB | V | ABC-2 type transporter | ||
HNJLMKBB_00347 | 4.5e-74 | K | COG3279 Response regulator of the LytR AlgR family | |||
HNJLMKBB_00348 | 1.8e-32 | S | Protein of unknown function (DUF3021) | |||
HNJLMKBB_00349 | 1.6e-123 | mta | K | Transcriptional | ||
HNJLMKBB_00350 | 8e-42 | ylxQ | J | ribosomal protein | ||
HNJLMKBB_00351 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
HNJLMKBB_00352 | 2.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
HNJLMKBB_00353 | 2.3e-81 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
HNJLMKBB_00354 | 1.2e-57 | brpA | K | Transcriptional | ||
HNJLMKBB_00355 | 8e-99 | metI | P | ABC transporter (Permease | ||
HNJLMKBB_00356 | 6.4e-188 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HNJLMKBB_00357 | 2e-263 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
HNJLMKBB_00358 | 3.2e-164 | metQ | M | Belongs to the NlpA lipoprotein family | ||
HNJLMKBB_00359 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
HNJLMKBB_00360 | 1.3e-46 | azlD | S | branched-chain amino acid | ||
HNJLMKBB_00361 | 3e-114 | azlC | E | AzlC protein | ||
HNJLMKBB_00362 | 2.8e-185 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
HNJLMKBB_00363 | 1.6e-61 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
HNJLMKBB_00364 | 7.4e-68 | 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 | |
HNJLMKBB_00365 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
HNJLMKBB_00366 | 5.9e-82 | nrdI | F | Belongs to the NrdI family | ||
HNJLMKBB_00367 | 3.8e-110 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
HNJLMKBB_00368 | 3.3e-92 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HNJLMKBB_00369 | 7.3e-94 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
HNJLMKBB_00370 | 2.2e-101 | ybhL | S | Belongs to the BI1 family | ||
HNJLMKBB_00371 | 1.1e-12 | ycdA | S | Domain of unknown function (DUF4352) | ||
HNJLMKBB_00372 | 3.1e-242 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HNJLMKBB_00373 | 1.8e-90 | K | transcriptional regulator | |||
HNJLMKBB_00374 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
HNJLMKBB_00375 | 7.2e-198 | 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 | |
HNJLMKBB_00376 | 1.2e-255 | 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 | ||
HNJLMKBB_00377 | 1.1e-133 | parB | K | Belongs to the ParB family | ||
HNJLMKBB_00378 | 2.1e-155 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
HNJLMKBB_00379 | 7.9e-155 | T | PhoQ Sensor | |||
HNJLMKBB_00380 | 3.6e-257 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
HNJLMKBB_00381 | 4.1e-225 | XK27_05470 | E | Methionine synthase | ||
HNJLMKBB_00382 | 3.2e-71 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
HNJLMKBB_00383 | 1.8e-44 | pspE | P | Rhodanese-like protein | ||
HNJLMKBB_00384 | 1e-104 | wecD | M | Acetyltransferase (GNAT) domain | ||
HNJLMKBB_00385 | 3e-209 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
HNJLMKBB_00386 | 2.6e-158 | GK | ROK family | |||
HNJLMKBB_00387 | 1.8e-71 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
HNJLMKBB_00388 | 1.9e-145 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
HNJLMKBB_00389 | 1.3e-70 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
HNJLMKBB_00390 | 5.2e-229 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
HNJLMKBB_00391 | 8.7e-140 | ykuT | M | mechanosensitive ion channel | ||
HNJLMKBB_00392 | 3.9e-87 | sigH | K | DNA-templated transcription, initiation | ||
HNJLMKBB_00394 | 5.6e-84 | T | proteins involved in stress response, homologs of TerZ and | |||
HNJLMKBB_00395 | 2.3e-77 | T | proteins involved in stress response, homologs of TerZ and | |||
HNJLMKBB_00396 | 2.8e-90 | T | proteins involved in stress response, homologs of TerZ and | |||
HNJLMKBB_00397 | 0.0 | 3.6.3.8 | P | cation transport ATPase | ||
HNJLMKBB_00398 | 3.9e-229 | malX | G | ABC transporter | ||
HNJLMKBB_00399 | 4.4e-250 | malF | P | ABC transporter (Permease | ||
HNJLMKBB_00400 | 9.8e-152 | malG | P | ABC transporter (Permease | ||
HNJLMKBB_00401 | 1.5e-219 | metE | 2.1.1.14 | E | Methionine synthase | |
HNJLMKBB_00402 | 1.5e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HNJLMKBB_00403 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HNJLMKBB_00404 | 3.6e-179 | KLT | Protein tyrosine kinase | |||
HNJLMKBB_00405 | 1.1e-17 | S | Protein of unknown function (DUF3021) | |||
HNJLMKBB_00406 | 1.5e-152 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
HNJLMKBB_00407 | 2.1e-272 | glnP | P | ABC transporter | ||
HNJLMKBB_00408 | 2.2e-123 | glnQ | E | abc transporter atp-binding protein | ||
HNJLMKBB_00409 | 2.9e-131 | murB | 1.3.1.98 | M | cell wall formation | |
HNJLMKBB_00410 | 5.2e-212 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
HNJLMKBB_00411 | 4.1e-139 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
HNJLMKBB_00412 | 2.3e-131 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
HNJLMKBB_00413 | 4.4e-205 | potD | P | spermidine putrescine ABC transporter | ||
HNJLMKBB_00414 | 1.7e-204 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
HNJLMKBB_00415 | 3.5e-08 | XK27_10305 | S | Domain of unknown function (DUF4651) | ||
HNJLMKBB_00416 | 1.8e-53 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
HNJLMKBB_00417 | 2.2e-08 | S | NTF2 fold immunity protein | |||
HNJLMKBB_00418 | 1.9e-112 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HNJLMKBB_00419 | 1e-187 | yeeE | S | Sulphur transport | ||
HNJLMKBB_00420 | 8.3e-37 | yeeD | O | sulfur carrier activity | ||
HNJLMKBB_00421 | 1.9e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HNJLMKBB_00422 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HNJLMKBB_00423 | 3.8e-41 | S | Domain of unknown function (DUF4430) | |||
HNJLMKBB_00424 | 5.2e-215 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
HNJLMKBB_00425 | 4.8e-201 | ilvE | 2.6.1.42 | E | Aminotransferase | |
HNJLMKBB_00426 | 3.7e-16 | S | Protein of unknown function (DUF2969) | |||
HNJLMKBB_00429 | 2.5e-204 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
HNJLMKBB_00431 | 7.4e-44 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
HNJLMKBB_00432 | 0.0 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNJLMKBB_00433 | 1.4e-158 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
HNJLMKBB_00434 | 1.5e-121 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
HNJLMKBB_00435 | 2.1e-252 | V | Glucan-binding protein C | |||
HNJLMKBB_00436 | 2.9e-111 | tcyB_2 | P | ABC transporter (permease) | ||
HNJLMKBB_00437 | 3.2e-153 | endA | F | DNA RNA non-specific endonuclease | ||
HNJLMKBB_00438 | 7.2e-26 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
HNJLMKBB_00439 | 7.7e-233 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HNJLMKBB_00440 | 6.9e-10 | S | Protein of unknown function (DUF1146) | |||
HNJLMKBB_00441 | 2e-157 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HNJLMKBB_00442 | 2.4e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
HNJLMKBB_00443 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HNJLMKBB_00444 | 1e-182 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
HNJLMKBB_00445 | 1.2e-82 | S | Putative small multi-drug export protein | |||
HNJLMKBB_00446 | 2.2e-41 | pepF | E | oligoendopeptidase F | ||
HNJLMKBB_00447 | 3.5e-214 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
HNJLMKBB_00448 | 6.1e-120 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
HNJLMKBB_00449 | 2.8e-165 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
HNJLMKBB_00450 | 3.3e-83 | yxjI | S | LURP-one-related | ||
HNJLMKBB_00451 | 6.4e-131 | 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 | |
HNJLMKBB_00452 | 4.8e-157 | 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 | ||
HNJLMKBB_00453 | 7.9e-263 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
HNJLMKBB_00454 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HNJLMKBB_00455 | 8.2e-168 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HNJLMKBB_00456 | 9.9e-135 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
HNJLMKBB_00457 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
HNJLMKBB_00459 | 3e-51 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
HNJLMKBB_00460 | 4.3e-22 | |||||
HNJLMKBB_00461 | 2e-217 | EGP | Transmembrane secretion effector | |||
HNJLMKBB_00462 | 1e-257 | yheS_2 | S | ATPase components of ABC transporters with duplicated ATPase domains | ||
HNJLMKBB_00463 | 3.8e-291 | yfiB1 | V | abc transporter atp-binding protein | ||
HNJLMKBB_00464 | 1.9e-99 | pvaA | M | lytic transglycosylase activity | ||
HNJLMKBB_00465 | 1.9e-178 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
HNJLMKBB_00466 | 1.7e-119 | 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 | |
HNJLMKBB_00467 | 3.3e-217 | yeaB | K | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
HNJLMKBB_00468 | 1.3e-249 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HNJLMKBB_00469 | 3.6e-28 | XK27_05745 | ||||
HNJLMKBB_00470 | 5.4e-225 | mutY | L | A G-specific adenine glycosylase | ||
HNJLMKBB_00472 | 3.2e-33 | |||||
HNJLMKBB_00473 | 3.7e-182 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
HNJLMKBB_00474 | 1e-34 | ykuJ | S | protein conserved in bacteria | ||
HNJLMKBB_00475 | 5.8e-118 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
HNJLMKBB_00476 | 6.4e-131 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNJLMKBB_00477 | 3.1e-78 | feoA | P | FeoA domain protein | ||
HNJLMKBB_00478 | 6.5e-232 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HNJLMKBB_00479 | 5.5e-144 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
HNJLMKBB_00480 | 5.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HNJLMKBB_00481 | 8.9e-48 | yajC | U | protein transport | ||
HNJLMKBB_00482 | 7.2e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HNJLMKBB_00483 | 9.9e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
HNJLMKBB_00486 | 3.1e-113 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
HNJLMKBB_00487 | 9.7e-170 | vraS | 2.7.13.3 | T | Histidine kinase | |
HNJLMKBB_00488 | 4.6e-137 | yqeM | Q | Methyltransferase domain protein | ||
HNJLMKBB_00489 | 7.7e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
HNJLMKBB_00490 | 8.4e-82 | entB | 3.5.1.19 | Q | Isochorismatase family | |
HNJLMKBB_00491 | 6e-103 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
HNJLMKBB_00492 | 1.2e-117 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HNJLMKBB_00493 | 7.7e-49 | yhbY | J | RNA-binding protein | ||
HNJLMKBB_00494 | 3.8e-171 | rmuC | S | RmuC domain protein | ||
HNJLMKBB_00495 | 8.6e-116 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HNJLMKBB_00496 | 3.9e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
HNJLMKBB_00497 | 3.2e-161 | rsgA | 3.1.3.100 | G | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
HNJLMKBB_00499 | 6.5e-108 | yvyE | 3.4.13.9 | S | YigZ family | |
HNJLMKBB_00500 | 3.4e-247 | comFA | L | Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
HNJLMKBB_00501 | 2.6e-83 | comFC | K | competence protein | ||
HNJLMKBB_00502 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HNJLMKBB_00503 | 6.2e-108 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
HNJLMKBB_00504 | 2.4e-220 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
HNJLMKBB_00505 | 3e-38 | ptsH | G | phosphocarrier protein Hpr | ||
HNJLMKBB_00506 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
HNJLMKBB_00507 | 1.3e-128 | 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 | ||
HNJLMKBB_00508 | 1.7e-17 | XK27_00735 | ||||
HNJLMKBB_00509 | 3.9e-136 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNJLMKBB_00510 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
HNJLMKBB_00511 | 2.5e-129 | pepC | 3.4.22.40 | E | aminopeptidase | |
HNJLMKBB_00512 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNJLMKBB_00513 | 4.3e-109 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
HNJLMKBB_00514 | 1.1e-226 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HNJLMKBB_00516 | 1.3e-173 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HNJLMKBB_00517 | 1.2e-211 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
HNJLMKBB_00518 | 3.2e-133 | XK27_00785 | S | CAAX protease self-immunity | ||
HNJLMKBB_00519 | 2.1e-236 | EGP | Major facilitator Superfamily | |||
HNJLMKBB_00520 | 6.2e-67 | rmaI | K | Transcriptional regulator, MarR family | ||
HNJLMKBB_00521 | 2.3e-88 | maa | 2.3.1.79 | GK | Maltose O-acetyltransferase | |
HNJLMKBB_00522 | 3.9e-93 | S | N-acetylphosphatidylethanolamine-hydrolysing phospholipas activity | |||
HNJLMKBB_00523 | 5e-290 | asp1 | S | Accessory Sec system protein Asp1 | ||
HNJLMKBB_00524 | 3.6e-186 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
HNJLMKBB_00525 | 1.3e-105 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HNJLMKBB_00526 | 0.0 | ydaO | E | amino acid | ||
HNJLMKBB_00527 | 7.7e-100 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
HNJLMKBB_00528 | 1e-104 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
HNJLMKBB_00529 | 8e-230 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
HNJLMKBB_00530 | 1e-204 | 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 | ||
HNJLMKBB_00531 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
HNJLMKBB_00532 | 0.0 | WQ51_06230 | S | ABC transporter | ||
HNJLMKBB_00533 | 1.4e-142 | cmpC | S | abc transporter atp-binding protein | ||
HNJLMKBB_00534 | 4.9e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HNJLMKBB_00535 | 4.9e-148 | 2.4.1.83 | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
HNJLMKBB_00537 | 5.8e-162 | T | Diguanylate cyclase | |||
HNJLMKBB_00538 | 2.2e-35 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
HNJLMKBB_00539 | 1.7e-60 | fruR | K | transcriptional | ||
HNJLMKBB_00540 | 1.6e-36 | yneF | S | UPF0154 protein | ||
HNJLMKBB_00541 | 1.5e-149 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HNJLMKBB_00542 | 1.3e-184 | 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 | |
HNJLMKBB_00543 | 6.6e-98 | XK27_09740 | S | Phosphoesterase | ||
HNJLMKBB_00544 | 8.3e-87 | ykuL | S | CBS domain | ||
HNJLMKBB_00545 | 1.5e-133 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
HNJLMKBB_00546 | 1.3e-163 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
HNJLMKBB_00547 | 1.2e-25 | WQ51_00785 | ||||
HNJLMKBB_00548 | 7.4e-247 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
HNJLMKBB_00549 | 8.7e-78 | yueI | S | Protein of unknown function (DUF1694) | ||
HNJLMKBB_00550 | 5.3e-81 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HNJLMKBB_00551 | 0.0 | V | ABC transporter (Permease | |||
HNJLMKBB_00552 | 1.9e-124 | V | abc transporter atp-binding protein | |||
HNJLMKBB_00553 | 0.0 | |||||
HNJLMKBB_00554 | 0.0 | bcsA | 2.4.1.12 | GT2 | M | COG1215 Glycosyltransferases, probably involved in cell wall biogenesis |
HNJLMKBB_00555 | 1.6e-120 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
HNJLMKBB_00556 | 1e-85 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
HNJLMKBB_00557 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HNJLMKBB_00558 | 1.5e-56 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
HNJLMKBB_00559 | 1.7e-84 | XK27_03610 | K | Gnat family | ||
HNJLMKBB_00560 | 1e-90 | yybC | ||||
HNJLMKBB_00561 | 4.9e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
HNJLMKBB_00562 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HNJLMKBB_00563 | 8.1e-84 | V | VanZ like family | |||
HNJLMKBB_00564 | 8.8e-12 | D | nuclear chromosome segregation | |||
HNJLMKBB_00566 | 1.3e-73 | 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 | ||
HNJLMKBB_00567 | 1.3e-157 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
HNJLMKBB_00568 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HNJLMKBB_00569 | 1.4e-119 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HNJLMKBB_00570 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HNJLMKBB_00571 | 1.5e-245 | epsU | S | Polysaccharide biosynthesis protein | ||
HNJLMKBB_00572 | 1.4e-172 | |||||
HNJLMKBB_00573 | 2.2e-34 | nrdH | O | Glutaredoxin | ||
HNJLMKBB_00574 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HNJLMKBB_00575 | 3.8e-184 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HNJLMKBB_00576 | 6.7e-96 | 3.1.3.18 | S | IA, variant 1 | ||
HNJLMKBB_00577 | 3.2e-116 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like proteins CidA and or CidB. The LrgAB and CidAB proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
HNJLMKBB_00578 | 3.5e-56 | lrgA | S | Effector of murein hydrolase LrgA | ||
HNJLMKBB_00580 | 2.7e-58 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
HNJLMKBB_00581 | 1.6e-168 | manN | G | PTS system mannose fructose sorbose family IID component | ||
HNJLMKBB_00582 | 1.7e-116 | manM | G | pts system | ||
HNJLMKBB_00583 | 4.9e-174 | manL | 2.7.1.191 | G | pts system | |
HNJLMKBB_00584 | 2.2e-66 | manO | S | Protein conserved in bacteria | ||
HNJLMKBB_00585 | 4.4e-166 | dnaI | L | Primosomal protein DnaI | ||
HNJLMKBB_00586 | 1.6e-216 | dnaB | L | Replication initiation and membrane attachment | ||
HNJLMKBB_00587 | 3e-81 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HNJLMKBB_00588 | 2.9e-122 | T | PhoQ Sensor | |||
HNJLMKBB_00590 | 2.5e-07 | |||||
HNJLMKBB_00591 | 7e-35 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HNJLMKBB_00592 | 1.7e-17 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HNJLMKBB_00593 | 1.1e-28 | |||||
HNJLMKBB_00594 | 3.5e-29 | |||||
HNJLMKBB_00595 | 1.3e-125 | dnaD | ||||
HNJLMKBB_00596 | 2.8e-179 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
HNJLMKBB_00597 | 1.9e-92 | 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 | |
HNJLMKBB_00598 | 7e-144 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
HNJLMKBB_00599 | 1.3e-193 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
HNJLMKBB_00600 | 2.2e-76 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
HNJLMKBB_00601 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
HNJLMKBB_00602 | 8.6e-31 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HNJLMKBB_00603 | 8e-163 | yjlA | EG | membrane | ||
HNJLMKBB_00604 | 6e-129 | dnaE | 2.7.7.7 | L | DNA polymerase | |
HNJLMKBB_00605 | 1e-187 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
HNJLMKBB_00606 | 2.7e-277 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HNJLMKBB_00608 | 0.0 | typA | T | GTP-binding protein TypA | ||
HNJLMKBB_00609 | 5.9e-17 | glk | 2.7.1.2 | G | Glucokinase | |
HNJLMKBB_00610 | 4.8e-35 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
HNJLMKBB_00611 | 1.7e-179 | scrR | K | Transcriptional regulator | ||
HNJLMKBB_00612 | 1.5e-288 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
HNJLMKBB_00613 | 1.4e-92 | adk | 2.7.4.3 | F | topology modulation protein | |
HNJLMKBB_00614 | 3e-248 | 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 | |
HNJLMKBB_00615 | 4.4e-79 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HNJLMKBB_00616 | 9.7e-36 | XK27_09805 | S | MORN repeat protein | ||
HNJLMKBB_00617 | 2.2e-108 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
HNJLMKBB_00618 | 3.3e-236 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
HNJLMKBB_00619 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HNJLMKBB_00620 | 4.4e-77 | 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 | ||
HNJLMKBB_00621 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
HNJLMKBB_00622 | 9.2e-92 | K | LysR substrate binding domain | |||
HNJLMKBB_00623 | 3.2e-133 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HNJLMKBB_00624 | 2.1e-114 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
HNJLMKBB_00625 | 2.3e-19 | V | Type III restriction enzyme, res subunit | |||
HNJLMKBB_00626 | 3.3e-147 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
HNJLMKBB_00627 | 1.2e-255 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
HNJLMKBB_00628 | 3.9e-150 | cobQ | S | glutamine amidotransferase | ||
HNJLMKBB_00629 | 6.4e-113 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
HNJLMKBB_00630 | 2.4e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HNJLMKBB_00631 | 1e-209 | S | phospholipase Carboxylesterase | |||
HNJLMKBB_00632 | 5.6e-231 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HNJLMKBB_00633 | 4.8e-140 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
HNJLMKBB_00634 | 7.9e-100 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
HNJLMKBB_00635 | 3.7e-185 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HNJLMKBB_00636 | 4.1e-63 | 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 | ||
HNJLMKBB_00637 | 7.7e-118 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
HNJLMKBB_00638 | 2.9e-25 | |||||
HNJLMKBB_00639 | 7.7e-97 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
HNJLMKBB_00640 | 8.3e-257 | 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 | |
HNJLMKBB_00641 | 2.8e-114 | S | HAD hydrolase, family IA, variant 3 | |||
HNJLMKBB_00642 | 1.8e-256 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HNJLMKBB_00643 | 3e-192 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
HNJLMKBB_00644 | 2.3e-90 | yacP | S | RNA-binding protein containing a PIN domain | ||
HNJLMKBB_00645 | 9.7e-135 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HNJLMKBB_00647 | 4.4e-30 | |||||
HNJLMKBB_00648 | 7.6e-261 | |||||
HNJLMKBB_00649 | 6.3e-157 | yddE | S | AAA-like domain | ||
HNJLMKBB_00650 | 3.1e-160 | S | Conjugative transposon protein TcpC | |||
HNJLMKBB_00651 | 3.2e-33 | |||||
HNJLMKBB_00652 | 7.9e-70 | S | TcpE family | |||
HNJLMKBB_00653 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
HNJLMKBB_00654 | 1.7e-193 | abf | G | Glycosyl hydrolases family 43 | ||
HNJLMKBB_00655 | 1e-242 | G | Bacterial extracellular solute-binding protein | |||
HNJLMKBB_00656 | 1.6e-134 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HNJLMKBB_00657 | 4.8e-179 | clcA_2 | P | Chloride transporter, ClC family | ||
HNJLMKBB_00658 | 2e-149 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
HNJLMKBB_00659 | 1.2e-64 | S | Protein of unknown function (DUF1697) | |||
HNJLMKBB_00660 | 3.6e-70 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | G | Belongs to the glycosyl hydrolase 68 family |
HNJLMKBB_00661 | 5.7e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HNJLMKBB_00662 | 3.7e-105 | clpP | 3.4.21.92 | OU | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
HNJLMKBB_00663 | 4.4e-74 | ylbF | S | Belongs to the UPF0342 family | ||
HNJLMKBB_00664 | 1.9e-46 | ylbG | S | UPF0298 protein | ||
HNJLMKBB_00665 | 5.6e-112 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
HNJLMKBB_00666 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
HNJLMKBB_00667 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
HNJLMKBB_00668 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
HNJLMKBB_00669 | 2e-143 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
HNJLMKBB_00670 | 2.9e-145 | cah | 4.2.1.1 | P | carbonic anhydrase | |
HNJLMKBB_00671 | 4.8e-76 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
HNJLMKBB_00673 | 5.9e-126 | V | abc transporter atp-binding protein | |||
HNJLMKBB_00674 | 2.8e-91 | tetR | K | transcriptional regulator | ||
HNJLMKBB_00675 | 3.5e-263 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
HNJLMKBB_00676 | 3.8e-54 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
HNJLMKBB_00677 | 9.7e-147 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
HNJLMKBB_00678 | 2.8e-105 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
HNJLMKBB_00679 | 9.9e-219 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
HNJLMKBB_00680 | 2.7e-205 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
HNJLMKBB_00681 | 4.7e-81 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
HNJLMKBB_00682 | 1.4e-163 | K | helix_turn _helix lactose operon repressor | |||
HNJLMKBB_00683 | 1.4e-85 | I | alpha/beta hydrolase fold | |||
HNJLMKBB_00684 | 2.9e-104 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
HNJLMKBB_00685 | 8.7e-237 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
HNJLMKBB_00686 | 0.0 | GM | domain, Protein | |||
HNJLMKBB_00687 | 3.5e-137 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
HNJLMKBB_00688 | 2.5e-118 | ylfI | S | tigr01906 | ||
HNJLMKBB_00689 | 4.7e-140 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HNJLMKBB_00690 | 1.2e-57 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
HNJLMKBB_00692 | 4.3e-95 | ywlG | S | Belongs to the UPF0340 family | ||
HNJLMKBB_00693 | 6e-126 | treR | K | trehalose operon | ||
HNJLMKBB_00694 | 2.4e-184 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HNJLMKBB_00695 | 0.0 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
HNJLMKBB_00696 | 1.4e-223 | ytfP | S | Flavoprotein | ||
HNJLMKBB_00698 | 3.1e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HNJLMKBB_00699 | 1.9e-67 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
HNJLMKBB_00700 | 4.7e-168 | fhuR | K | transcriptional regulator (lysR family) | ||
HNJLMKBB_00701 | 1.3e-76 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HNJLMKBB_00702 | 5.5e-161 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HNJLMKBB_00703 | 4.8e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HNJLMKBB_00704 | 4.4e-223 | vncS | 2.7.13.3 | T | Histidine kinase | |
HNJLMKBB_00705 | 3.4e-32 | K | Response regulator receiver domain protein | |||
HNJLMKBB_00707 | 5.4e-303 | yloV | S | kinase related to dihydroxyacetone kinase | ||
HNJLMKBB_00708 | 1.4e-57 | asp | S | cog cog1302 | ||
HNJLMKBB_00709 | 1.1e-245 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HNJLMKBB_00710 | 1e-221 | rodA | D | Belongs to the SEDS family | ||
HNJLMKBB_00711 | 9.1e-270 | lacS | G | transporter | ||
HNJLMKBB_00712 | 1.6e-175 | saeS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
HNJLMKBB_00713 | 1.4e-127 | K | response regulator | |||
HNJLMKBB_00714 | 2.4e-97 | S | Signal peptide protein, YSIRK family | |||
HNJLMKBB_00715 | 9.8e-118 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
HNJLMKBB_00716 | 1.8e-95 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HNJLMKBB_00717 | 1.3e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HNJLMKBB_00718 | 2.9e-10 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HNJLMKBB_00719 | 1.4e-213 | vex1 | V | Efflux ABC transporter, permease protein | ||
HNJLMKBB_00720 | 2.7e-82 | secA2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
HNJLMKBB_00721 | 1e-78 | asp3 | S | Accessory Sec system protein Asp3 | ||
HNJLMKBB_00722 | 1.6e-111 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
HNJLMKBB_00723 | 8.4e-93 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
HNJLMKBB_00724 | 6.6e-198 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HNJLMKBB_00725 | 2.4e-16 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
HNJLMKBB_00726 | 9e-122 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HNJLMKBB_00727 | 2.1e-77 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HNJLMKBB_00728 | 3.9e-85 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
HNJLMKBB_00729 | 6.5e-87 | XK27_09675 | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
HNJLMKBB_00730 | 2.8e-38 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HNJLMKBB_00731 | 1.8e-144 | P | molecular chaperone | |||
HNJLMKBB_00732 | 5.5e-98 | S | Carbohydrate-binding domain-containing protein Cthe_2159 | |||
HNJLMKBB_00733 | 2.4e-47 | XK27_08075 | M | glycosyl transferase family 2 | ||
HNJLMKBB_00734 | 7e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
HNJLMKBB_00735 | 4.4e-112 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
HNJLMKBB_00736 | 1.2e-244 | 2.7.13.3 | T | protein histidine kinase activity | ||
HNJLMKBB_00737 | 1.8e-218 | dcuS | 2.7.13.3 | T | protein histidine kinase activity | |
HNJLMKBB_00738 | 1.8e-59 | S | Protein of unknown function (DUF3290) | |||
HNJLMKBB_00739 | 3.4e-104 | S | Protein of unknown function (DUF421) | |||
HNJLMKBB_00740 | 2.4e-16 | csbD | S | CsbD-like | ||
HNJLMKBB_00742 | 9.8e-68 | S | 6-bladed beta-propeller | |||
HNJLMKBB_00743 | 3e-209 | CO | amine dehydrogenase activity | |||
HNJLMKBB_00744 | 9.7e-22 | |||||
HNJLMKBB_00745 | 2.6e-225 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
HNJLMKBB_00746 | 5.1e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HNJLMKBB_00747 | 1.5e-62 | GT4 | M | transferase activity, transferring glycosyl groups | ||
HNJLMKBB_00748 | 2.7e-224 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
HNJLMKBB_00749 | 9.3e-175 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
HNJLMKBB_00750 | 2.6e-43 | copA | 3.6.3.54 | P | P-type ATPase | |
HNJLMKBB_00751 | 1.4e-30 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
HNJLMKBB_00752 | 6e-191 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HNJLMKBB_00753 | 1.5e-113 | papP | P | ABC transporter (Permease | ||
HNJLMKBB_00754 | 5.6e-36 | secA2 | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
HNJLMKBB_00755 | 6.3e-282 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
HNJLMKBB_00758 | 2.6e-24 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HNJLMKBB_00759 | 4.5e-97 | mvaS | 2.3.3.10 | I | synthase | |
HNJLMKBB_00760 | 1.4e-226 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HNJLMKBB_00761 | 3e-78 | K | hmm pf08876 | |||
HNJLMKBB_00762 | 2.6e-247 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HNJLMKBB_00763 | 4.1e-136 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HNJLMKBB_00764 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
HNJLMKBB_00765 | 1.2e-50 | S | Protein of unknown function (DUF3397) | |||
HNJLMKBB_00766 | 1e-87 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HNJLMKBB_00767 | 7e-127 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
HNJLMKBB_00768 | 8.7e-162 | 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 | ||
HNJLMKBB_00769 | 6.4e-91 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
HNJLMKBB_00770 | 1.7e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HNJLMKBB_00771 | 1.3e-174 | sptS | 2.7.13.3 | T | Histidine kinase | |
HNJLMKBB_00772 | 8.3e-73 | argR | K | Regulates arginine biosynthesis genes | ||
HNJLMKBB_00773 | 2.2e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HNJLMKBB_00774 | 4e-45 | ftsL | D | cell division protein FtsL | ||
HNJLMKBB_00775 | 3.9e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HNJLMKBB_00776 | 6e-85 | |||||
HNJLMKBB_00777 | 1.1e-29 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
HNJLMKBB_00778 | 3.3e-112 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
HNJLMKBB_00779 | 1.4e-110 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
HNJLMKBB_00780 | 8e-188 | 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 | |
HNJLMKBB_00781 | 1.1e-217 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
HNJLMKBB_00782 | 3.3e-78 | ybbR | S | Protein conserved in bacteria | ||
HNJLMKBB_00783 | 1.3e-249 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HNJLMKBB_00784 | 1.3e-64 | gtrA | S | GtrA-like protein | ||
HNJLMKBB_00785 | 2.1e-119 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
HNJLMKBB_00786 | 8.5e-272 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
HNJLMKBB_00787 | 1.7e-24 | yjcE | P | NhaP-type Na H and K H antiporters | ||
HNJLMKBB_00788 | 8.6e-142 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
HNJLMKBB_00789 | 3.8e-238 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
HNJLMKBB_00790 | 8.7e-60 | |||||
HNJLMKBB_00791 | 5.9e-55 | |||||
HNJLMKBB_00792 | 1.5e-36 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HNJLMKBB_00793 | 3.4e-97 | J | Acetyltransferase (GNAT) domain | |||
HNJLMKBB_00794 | 1.2e-191 | S | dextransucrase activity | |||
HNJLMKBB_00795 | 1.3e-137 | tcyC2 | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNJLMKBB_00796 | 2.2e-73 | yxeN | P | ABC transporter, permease protein | ||
HNJLMKBB_00797 | 2.4e-50 | trxA | O | Belongs to the thioredoxin family | ||
HNJLMKBB_00798 | 1.2e-73 | yccU | S | CoA-binding protein | ||
HNJLMKBB_00799 | 1.6e-143 | tatD | L | Hydrolase, tatd | ||
HNJLMKBB_00800 | 1.1e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
HNJLMKBB_00801 | 2.2e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HNJLMKBB_00802 | 9.6e-236 | dltB | M | Membrane protein involved in D-alanine export | ||
HNJLMKBB_00803 | 9e-147 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HNJLMKBB_00804 | 6.4e-182 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
HNJLMKBB_00805 | 6.6e-184 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
HNJLMKBB_00806 | 2.4e-10 | S | dextransucrase activity | |||
HNJLMKBB_00807 | 1.2e-91 | mmuP | E | amino acid | ||
HNJLMKBB_00808 | 8.8e-173 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
HNJLMKBB_00809 | 2.2e-30 | S | Domain of unknown function (DUF1912) | |||
HNJLMKBB_00810 | 4.8e-13 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
HNJLMKBB_00811 | 4e-38 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
HNJLMKBB_00812 | 0.0 | lmrA1 | V | abc transporter atp-binding protein | ||
HNJLMKBB_00813 | 3e-75 | K | DNA-binding transcription factor activity | |||
HNJLMKBB_00814 | 2.5e-121 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
HNJLMKBB_00815 | 9.7e-129 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
HNJLMKBB_00816 | 5.8e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HNJLMKBB_00817 | 2.9e-165 | cpsY | K | Transcriptional regulator | ||
HNJLMKBB_00818 | 1.3e-133 | htpX | O | Belongs to the peptidase M48B family | ||
HNJLMKBB_00819 | 7.7e-92 | lemA | S | LemA family | ||
HNJLMKBB_00820 | 1.8e-176 | spd | F | DNA RNA non-specific endonuclease | ||
HNJLMKBB_00821 | 0.0 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNJLMKBB_00822 | 7.8e-10 | |||||
HNJLMKBB_00823 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
HNJLMKBB_00824 | 2.4e-223 | G | COG0457 FOG TPR repeat | |||
HNJLMKBB_00825 | 1e-147 | yubA | S | permease | ||
HNJLMKBB_00826 | 6.7e-37 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
HNJLMKBB_00827 | 1e-292 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
HNJLMKBB_00828 | 2.9e-27 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HNJLMKBB_00829 | 1.4e-13 | yidD | M | Could be involved in insertion of integral membrane proteins into the membrane | ||
HNJLMKBB_00830 | 4.9e-260 | trkH | P | Cation transport protein | ||
HNJLMKBB_00831 | 3.3e-107 | trkA | P | Potassium transporter peripheral membrane component | ||
HNJLMKBB_00832 | 6.5e-117 | yebC | M | Membrane | ||
HNJLMKBB_00833 | 1.3e-63 | ecsA_2 | V | abc transporter atp-binding protein | ||
HNJLMKBB_00834 | 3e-282 | XK27_00765 | ||||
HNJLMKBB_00835 | 9.6e-40 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
HNJLMKBB_00836 | 1.2e-214 | XK27_05110 | P | Chloride transporter ClC family | ||
HNJLMKBB_00837 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
HNJLMKBB_00839 | 6.8e-113 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
HNJLMKBB_00840 | 3e-93 | 2.3.1.128 | K | acetyltransferase | ||
HNJLMKBB_00841 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HNJLMKBB_00842 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HNJLMKBB_00843 | 6.4e-149 | czcD | P | cation diffusion facilitator family transporter | ||
HNJLMKBB_00844 | 2.5e-195 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
HNJLMKBB_00845 | 8.1e-76 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNJLMKBB_00846 | 5e-10 | S | Protein of unknown function (DUF4059) | |||
HNJLMKBB_00847 | 8e-171 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HNJLMKBB_00848 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HNJLMKBB_00849 | 3e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HNJLMKBB_00850 | 3.6e-285 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
HNJLMKBB_00851 | 2.4e-49 | L | COG1943 Transposase and inactivated derivatives | |||
HNJLMKBB_00852 | 1.3e-35 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
HNJLMKBB_00854 | 5.3e-256 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNJLMKBB_00855 | 2.7e-67 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
HNJLMKBB_00856 | 7.9e-123 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HNJLMKBB_00857 | 6.2e-91 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
HNJLMKBB_00858 | 2.3e-151 | S | hmm pf01594 | |||
HNJLMKBB_00859 | 4.7e-287 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HNJLMKBB_00860 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
HNJLMKBB_00861 | 4e-201 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
HNJLMKBB_00862 | 2.5e-104 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HNJLMKBB_00863 | 3.9e-190 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
HNJLMKBB_00864 | 2.5e-178 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
HNJLMKBB_00865 | 1e-29 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HNJLMKBB_00866 | 4.6e-242 | T | PhoQ Sensor | |||
HNJLMKBB_00867 | 5.5e-121 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HNJLMKBB_00869 | 1.5e-272 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
HNJLMKBB_00870 | 4.9e-80 | 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 | |
HNJLMKBB_00871 | 2.7e-86 | |||||
HNJLMKBB_00872 | 5e-90 | niaR | S | small molecule binding protein (contains 3H domain) | ||
HNJLMKBB_00873 | 4e-127 | K | DNA-binding helix-turn-helix protein | |||
HNJLMKBB_00875 | 4e-212 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
HNJLMKBB_00876 | 4.7e-168 | K | transcriptional regulator (lysR family) | |||
HNJLMKBB_00877 | 9e-161 | S | reductase | |||
HNJLMKBB_00878 | 2.8e-185 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
HNJLMKBB_00879 | 4.7e-32 | |||||
HNJLMKBB_00880 | 1.5e-101 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
HNJLMKBB_00881 | 7.4e-115 | 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 | |
HNJLMKBB_00882 | 8.4e-113 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
HNJLMKBB_00883 | 1.9e-182 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | glucose-1-phosphate adenylyltransferase |
HNJLMKBB_00884 | 2.6e-124 | agrA | KT | phosphorelay signal transduction system | ||
HNJLMKBB_00885 | 4.8e-201 | 2.7.13.3 | T | protein histidine kinase activity | ||
HNJLMKBB_00886 | 9e-156 | pstS | P | phosphate | ||
HNJLMKBB_00887 | 1.9e-156 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HNJLMKBB_00888 | 2.7e-146 | V | 'abc transporter, ATP-binding protein | |||
HNJLMKBB_00889 | 9.5e-33 | blpT | ||||
HNJLMKBB_00890 | 3.7e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HNJLMKBB_00891 | 3.7e-66 | silP | 1.9.3.1, 3.6.3.54 | S | cog cog4633 | |
HNJLMKBB_00892 | 6.3e-35 | copY | K | Copper transport repressor, CopY TcrY family | ||
HNJLMKBB_00893 | 2.9e-20 | copY | K | Copper transport repressor, CopY TcrY family | ||
HNJLMKBB_00894 | 1.2e-97 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HNJLMKBB_00895 | 4.2e-231 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HNJLMKBB_00896 | 1e-34 | clpC | O | Belongs to the ClpA ClpB family | ||
HNJLMKBB_00897 | 8e-120 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
HNJLMKBB_00898 | 7.1e-101 | yjbK | S | Adenylate cyclase | ||
HNJLMKBB_00899 | 1.5e-253 | V | abc transporter atp-binding protein | |||
HNJLMKBB_00900 | 2.2e-151 | XK27_10075 | S | abc transporter atp-binding protein | ||
HNJLMKBB_00901 | 1.7e-234 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
HNJLMKBB_00902 | 7.9e-123 | 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 | |
HNJLMKBB_00903 | 6.6e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HNJLMKBB_00904 | 8.2e-15 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
HNJLMKBB_00905 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HNJLMKBB_00906 | 2.6e-36 | S | Protein of unknown function (DUF554) | |||
HNJLMKBB_00907 | 1.4e-75 | S | Bacterial membrane protein, YfhO | |||
HNJLMKBB_00908 | 1.9e-219 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
HNJLMKBB_00909 | 5.8e-258 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HNJLMKBB_00910 | 8.1e-140 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
HNJLMKBB_00911 | 2e-100 | pncA | Q | isochorismatase | ||
HNJLMKBB_00912 | 6.1e-169 | copA | 3.6.3.54 | P | P-type ATPase | |
HNJLMKBB_00913 | 3.1e-12 | spxB | 1.2.3.3, 1.2.5.1 | C | Pyruvate flavodoxin/ferredoxin oxidoreductase, thiamine diP-bdg | |
HNJLMKBB_00914 | 0.0 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
HNJLMKBB_00915 | 1e-290 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HNJLMKBB_00916 | 6.6e-126 | macB_2 | V | FtsX-like permease family | ||
HNJLMKBB_00917 | 9.3e-211 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
HNJLMKBB_00918 | 2.3e-08 | sraP | UW | domain, Protein | ||
HNJLMKBB_00919 | 8.8e-22 | |||||
HNJLMKBB_00920 | 2.2e-10 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNJLMKBB_00921 | 6.9e-275 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
HNJLMKBB_00922 | 2.4e-83 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
HNJLMKBB_00923 | 4.9e-76 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
HNJLMKBB_00924 | 4.5e-177 | prmA | J | Ribosomal protein L11 methyltransferase | ||
HNJLMKBB_00925 | 8.6e-73 | |||||
HNJLMKBB_00926 | 1.7e-42 | |||||
HNJLMKBB_00928 | 4e-46 | K | Bacteriophage CI repressor helix-turn-helix domain | |||
HNJLMKBB_00929 | 1e-182 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
HNJLMKBB_00930 | 2.3e-73 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
HNJLMKBB_00931 | 0.0 | 3.5.1.28 | NU | amidase activity | ||
HNJLMKBB_00932 | 1.2e-92 | cbiQ | P | Cobalt transport protein | ||
HNJLMKBB_00933 | 3.5e-157 | P | ATPase activity | |||
HNJLMKBB_00934 | 5.2e-150 | cbiO2 | P | Zeta toxin | ||
HNJLMKBB_00935 | 0.0 | M | family 8 | |||
HNJLMKBB_00936 | 9.5e-175 | coiA | 3.6.4.12 | S | Competence protein | |
HNJLMKBB_00937 | 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 | ||
HNJLMKBB_00938 | 1.1e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HNJLMKBB_00939 | 1.2e-78 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
HNJLMKBB_00940 | 1.7e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
HNJLMKBB_00941 | 1.4e-107 | sufD | O | assembly protein SufD | ||
HNJLMKBB_00942 | 5.9e-238 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
HNJLMKBB_00943 | 1.4e-234 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
HNJLMKBB_00944 | 6.7e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
HNJLMKBB_00945 | 7.9e-89 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
HNJLMKBB_00946 | 8.5e-08 | N | PFAM Uncharacterised protein family UPF0150 | |||
HNJLMKBB_00947 | 4.5e-112 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
HNJLMKBB_00948 | 1.2e-68 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
HNJLMKBB_00949 | 2.2e-131 | ecsA | V | abc transporter atp-binding protein | ||
HNJLMKBB_00950 | 6e-73 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
HNJLMKBB_00954 | 2.8e-51 | spd | F | DNA RNA non-specific endonuclease | ||
HNJLMKBB_00955 | 6.6e-22 | xerS | L | Belongs to the 'phage' integrase family | ||
HNJLMKBB_00956 | 2.8e-307 | pacL | 3.6.3.8 | P | cation transport ATPase | |
HNJLMKBB_00957 | 1.8e-136 | rapZ | S | Displays ATPase and GTPase activities | ||
HNJLMKBB_00958 | 3.1e-181 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HNJLMKBB_00959 | 9.1e-192 | rgpF | GT2,GT4 | M | Rhamnan synthesis protein F | |
HNJLMKBB_00960 | 1.7e-177 | fruA | 2.7.1.202 | G | phosphotransferase system | |
HNJLMKBB_00961 | 2.8e-73 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HNJLMKBB_00962 | 4.6e-29 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
HNJLMKBB_00963 | 8.6e-235 | 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 | |
HNJLMKBB_00964 | 2e-123 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
HNJLMKBB_00965 | 2.1e-187 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HNJLMKBB_00967 | 6.5e-99 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
HNJLMKBB_00968 | 1.4e-150 | 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 |
HNJLMKBB_00969 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
HNJLMKBB_00972 | 2.4e-26 | V | Psort location CytoplasmicMembrane, score | |||
HNJLMKBB_00973 | 1.4e-27 | vex2 | V | abc transporter atp-binding protein | ||
HNJLMKBB_00974 | 1.9e-237 | vex3 | V | Efflux ABC transporter, permease protein | ||
HNJLMKBB_00975 | 4.2e-175 | thrC | 4.2.3.1 | E | Threonine synthase | |
HNJLMKBB_00976 | 2.7e-62 | norN | V | Mate efflux family protein | ||
HNJLMKBB_00977 | 2.2e-182 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HNJLMKBB_00978 | 1.6e-142 | P | PFAM binding-protein-dependent transport systems inner membrane component | |||
HNJLMKBB_00979 | 1e-138 | G | Binding-protein-dependent transport system inner membrane component | |||
HNJLMKBB_00980 | 1.7e-18 | S | Domain of unknown function (DUF4649) | |||
HNJLMKBB_00981 | 2.8e-177 | XK27_08835 | S | ABC transporter substrate binding protein | ||
HNJLMKBB_00982 | 2.5e-77 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
HNJLMKBB_00983 | 2.7e-105 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
HNJLMKBB_00984 | 3.9e-179 | 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) | |
HNJLMKBB_00985 | 1.8e-51 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
HNJLMKBB_00987 | 1.6e-99 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
HNJLMKBB_00988 | 7.4e-134 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
HNJLMKBB_00989 | 3.6e-140 | S | SseB protein N-terminal domain | |||
HNJLMKBB_00990 | 3.9e-99 | thiT | S | Thiamine transporter | ||
HNJLMKBB_00992 | 2e-157 | dprA | LU | DNA protecting protein DprA | ||
HNJLMKBB_00993 | 3.6e-67 | GK | ROK family | |||
HNJLMKBB_00994 | 5.8e-149 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
HNJLMKBB_00995 | 4.4e-166 | era | M | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HNJLMKBB_00997 | 6.5e-154 | XK27_09825 | V | abc transporter atp-binding protein | ||
HNJLMKBB_00998 | 3.4e-132 | yvfS | V | Transporter | ||
HNJLMKBB_00999 | 4.6e-88 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
HNJLMKBB_01000 | 4.4e-152 | licT | K | antiterminator | ||
HNJLMKBB_01001 | 4.1e-50 | 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 | ||
HNJLMKBB_01002 | 5.3e-231 | ycdB | P | peroxidase | ||
HNJLMKBB_01003 | 9.1e-30 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
HNJLMKBB_01004 | 2.1e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
HNJLMKBB_01005 | 5.3e-136 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HNJLMKBB_01006 | 2.7e-68 | K | LytTr DNA-binding domain | |||
HNJLMKBB_01008 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HNJLMKBB_01009 | 5.1e-22 | K | Transcriptional | |||
HNJLMKBB_01011 | 1.2e-29 | degV | S | DegV family | ||
HNJLMKBB_01012 | 2.5e-121 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HNJLMKBB_01013 | 1.8e-96 | corA | P | COG0598 Mg2 and Co2 transporters | ||
HNJLMKBB_01014 | 1e-156 | yvgN | C | reductase | ||
HNJLMKBB_01015 | 3.3e-97 | yoaK | S | Protein of unknown function (DUF1275) | ||
HNJLMKBB_01016 | 2.1e-188 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
HNJLMKBB_01017 | 3.1e-122 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
HNJLMKBB_01018 | 1.8e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HNJLMKBB_01019 | 1.2e-54 | yabA | L | Involved in initiation control of chromosome replication | ||
HNJLMKBB_01020 | 3.7e-83 | yaaT | S | stage 0 sporulation protein | ||
HNJLMKBB_01021 | 1.9e-19 | 2.7.13.3 | T | GHKL domain | ||
HNJLMKBB_01022 | 8.1e-131 | rr02 | KT | response regulator | ||
HNJLMKBB_01023 | 6.6e-81 | smpB | O | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
HNJLMKBB_01024 | 5.7e-277 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
HNJLMKBB_01025 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HNJLMKBB_01027 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HNJLMKBB_01028 | 1.5e-36 | ylqC | L | Belongs to the UPF0109 family | ||
HNJLMKBB_01029 | 3e-133 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
HNJLMKBB_01030 | 6.6e-139 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
HNJLMKBB_01031 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
HNJLMKBB_01032 | 1.1e-71 | soxS | K | Helix-turn-helix domain | ||
HNJLMKBB_01033 | 1.3e-234 | L | Transposase | |||
HNJLMKBB_01034 | 4.6e-152 | Z012_04635 | K | sequence-specific DNA binding | ||
HNJLMKBB_01035 | 9e-75 | XK27_03180 | T | universal stress protein | ||
HNJLMKBB_01036 | 1.7e-179 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
HNJLMKBB_01037 | 1.9e-138 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
HNJLMKBB_01038 | 1e-173 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
HNJLMKBB_01039 | 5.5e-43 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
HNJLMKBB_01040 | 1.7e-122 | rrmA | 2.1.1.187 | Q | methyltransferase | |
HNJLMKBB_01041 | 2e-140 | S | HAD hydrolase, family IA, variant | |||
HNJLMKBB_01042 | 4.6e-146 | yidA | S | hydrolases of the HAD superfamily | ||
HNJLMKBB_01043 | 3.4e-65 | murM | 2.3.2.10, 2.3.2.16 | V | protein involved in methicillin resistance | |
HNJLMKBB_01044 | 2e-219 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HNJLMKBB_01045 | 2e-135 | stp | 3.1.3.16 | T | phosphatase | |
HNJLMKBB_01046 | 3e-184 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
HNJLMKBB_01047 | 1.7e-100 | desR | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
HNJLMKBB_01048 | 6.8e-237 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HNJLMKBB_01049 | 6.8e-90 | comEA | L | COG1555 DNA uptake protein and related DNA-binding proteins | ||
HNJLMKBB_01050 | 4.3e-77 | plsC | 2.3.1.51 | I | Acyltransferase | |
HNJLMKBB_01055 | 6.7e-26 | S | Bacteriocin class II with double-glycine leader peptide | |||
HNJLMKBB_01056 | 2.2e-41 | S | Sugar efflux transporter for intercellular exchange | |||
HNJLMKBB_01057 | 3.4e-203 | P | FtsX-like permease family | |||
HNJLMKBB_01058 | 3.1e-14 | V | abc transporter atp-binding protein | |||
HNJLMKBB_01059 | 4.9e-174 | yeiH | S | membrane | ||
HNJLMKBB_01061 | 3.1e-187 | phoH | T | phosphate starvation-inducible protein PhoH | ||
HNJLMKBB_01062 | 2.1e-62 | sip | M | LysM domain protein | ||
HNJLMKBB_01063 | 1.2e-76 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
HNJLMKBB_01064 | 2e-106 | K | Transcriptional regulator | |||
HNJLMKBB_01065 | 2.1e-100 | jag | S | RNA-binding protein | ||
HNJLMKBB_01066 | 1.6e-11 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HNJLMKBB_01067 | 9.3e-49 | 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 | ||
HNJLMKBB_01068 | 3.2e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HNJLMKBB_01069 | 1.7e-91 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HNJLMKBB_01070 | 1.8e-292 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HNJLMKBB_01072 | 2.3e-226 | rnjB | S | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HNJLMKBB_01073 | 1.3e-79 | dnaE | 2.7.7.7 | L | DNA polymerase | |
HNJLMKBB_01074 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HNJLMKBB_01075 | 3.2e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
HNJLMKBB_01076 | 3.3e-26 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HNJLMKBB_01077 | 6.3e-193 | mccF | V | LD-carboxypeptidase | ||
HNJLMKBB_01078 | 5.3e-13 | S | integral membrane protein | |||
HNJLMKBB_01079 | 1.7e-117 | M | Pfam SNARE associated Golgi protein | |||
HNJLMKBB_01080 | 3.5e-32 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
HNJLMKBB_01081 | 7.7e-169 | amiC | P | ABC transporter (Permease | ||
HNJLMKBB_01082 | 1.3e-165 | amiD | P | ABC transporter (Permease | ||
HNJLMKBB_01084 | 2.3e-240 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
HNJLMKBB_01085 | 4.4e-62 | rplQ | J | ribosomal protein l17 | ||
HNJLMKBB_01086 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNJLMKBB_01087 | 1.9e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
HNJLMKBB_01088 | 4e-57 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
HNJLMKBB_01089 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HNJLMKBB_01090 | 2.7e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
HNJLMKBB_01091 | 2.1e-114 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
HNJLMKBB_01092 | 2.1e-230 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
HNJLMKBB_01093 | 5.7e-58 | rplO | J | binds to the 23S rRNA | ||
HNJLMKBB_01094 | 1.9e-23 | rpmD | J | ribosomal protein l30 | ||
HNJLMKBB_01095 | 1.3e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HNJLMKBB_01096 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
HNJLMKBB_01097 | 6.6e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
HNJLMKBB_01098 | 1.2e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
HNJLMKBB_01099 | 1.5e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HNJLMKBB_01100 | 1.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
HNJLMKBB_01101 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HNJLMKBB_01102 | 3.9e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HNJLMKBB_01103 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HNJLMKBB_01104 | 3.5e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HNJLMKBB_01105 | 1.1e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HNJLMKBB_01106 | 1.6e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HNJLMKBB_01107 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
HNJLMKBB_01108 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HNJLMKBB_01109 | 6.8e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
HNJLMKBB_01110 | 2.4e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HNJLMKBB_01111 | 5.4e-52 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HNJLMKBB_01112 | 1.4e-70 | S | QueT transporter | |||
HNJLMKBB_01114 | 1.3e-108 | S | unusual protein kinase | |||
HNJLMKBB_01115 | 8.7e-105 | estA | E | Lysophospholipase L1 and related esterases | ||
HNJLMKBB_01116 | 6.6e-41 | cvpA | S | toxin biosynthetic process | ||
HNJLMKBB_01117 | 2.1e-258 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
HNJLMKBB_01118 | 3e-243 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
HNJLMKBB_01119 | 3.3e-132 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
HNJLMKBB_01120 | 2.3e-23 | MA20_06245 | S | yiaA/B two helix domain | ||
HNJLMKBB_01121 | 1.7e-93 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
HNJLMKBB_01122 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
HNJLMKBB_01123 | 1e-148 | XK27_08360 | S | EDD domain protein, DegV family | ||
HNJLMKBB_01124 | 5.4e-77 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
HNJLMKBB_01125 | 2e-131 | yxkH | G | deacetylase | ||
HNJLMKBB_01126 | 1.1e-170 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
HNJLMKBB_01127 | 1.5e-59 | yaaA | S | S4 domain protein YaaA | ||
HNJLMKBB_01128 | 3.2e-203 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
HNJLMKBB_01129 | 0.0 | S | dextransucrase activity | |||
HNJLMKBB_01130 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HNJLMKBB_01131 | 4.3e-80 | hmpT | S | cog cog4720 | ||
HNJLMKBB_01132 | 1.5e-135 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
HNJLMKBB_01133 | 2e-100 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HNJLMKBB_01134 | 3e-40 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
HNJLMKBB_01135 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HNJLMKBB_01136 | 2.4e-110 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
HNJLMKBB_01137 | 8.6e-10 | S | D-Ala-teichoic acid biosynthesis protein | |||
HNJLMKBB_01138 | 4e-133 | XK27_10035 | V | abc transporter atp-binding protein | ||
HNJLMKBB_01139 | 1.6e-76 | 3.5.1.28 | M | domain protein | ||
HNJLMKBB_01140 | 1.7e-196 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
HNJLMKBB_01141 | 1.8e-273 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
HNJLMKBB_01142 | 1.6e-285 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
HNJLMKBB_01143 | 6.7e-279 | opuD | M | Belongs to the BCCT transporter (TC 2.A.15) family | ||
HNJLMKBB_01144 | 3.4e-109 | S | oxidoreductase | |||
HNJLMKBB_01145 | 6.2e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
HNJLMKBB_01146 | 5.1e-86 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
HNJLMKBB_01147 | 1.1e-44 | clpE | O | Belongs to the ClpA ClpB family | ||
HNJLMKBB_01148 | 7.8e-27 | P | Hemerythrin HHE cation binding domain protein | |||
HNJLMKBB_01152 | 8.1e-120 | yoaK | S | Protein of unknown function (DUF1275) | ||
HNJLMKBB_01153 | 8e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HNJLMKBB_01154 | 1e-265 | carB | 6.3.5.5 | F | carbamoyl-phosphate synthetase ammonia chain | |
HNJLMKBB_01155 | 1.3e-125 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HNJLMKBB_01156 | 8.7e-254 | cycA | E | permease | ||
HNJLMKBB_01158 | 1.6e-186 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
HNJLMKBB_01159 | 3.3e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HNJLMKBB_01160 | 1.5e-86 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
HNJLMKBB_01161 | 1.9e-141 | miaA | 2.5.1.75 | J | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
HNJLMKBB_01162 | 8.2e-44 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
HNJLMKBB_01163 | 2e-200 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HNJLMKBB_01164 | 2.3e-82 | mutF | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
HNJLMKBB_01165 | 7.7e-52 | V | ABC-2 family transporter protein | |||
HNJLMKBB_01166 | 3.1e-69 | argR | K | Regulates arginine biosynthesis genes | ||
HNJLMKBB_01167 | 1.1e-56 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
HNJLMKBB_01168 | 2.6e-22 | 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) | |
HNJLMKBB_01169 | 3.2e-133 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
HNJLMKBB_01170 | 7.9e-100 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
HNJLMKBB_01171 | 1.8e-84 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination | |
HNJLMKBB_01172 | 8.1e-177 | 4.1.1.37 | H | Uroporphyrinogen decarboxylase (URO-D) | ||
HNJLMKBB_01173 | 4.3e-197 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNJLMKBB_01174 | 6.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HNJLMKBB_01175 | 2.8e-24 | secE | U | Belongs to the SecE SEC61-gamma family | ||
HNJLMKBB_01176 | 0.0 | mprF | 2.3.2.3 | J | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
HNJLMKBB_01177 | 2e-102 | yvfS | V | Transporter | ||
HNJLMKBB_01178 | 1.1e-80 | cdd | 2.4.2.4, 3.5.4.5 | F | cytidine deaminase activity | |
HNJLMKBB_01179 | 5.3e-240 | agcS | E | (Alanine) symporter | ||
HNJLMKBB_01180 | 2.5e-194 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HNJLMKBB_01181 | 3e-81 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
HNJLMKBB_01182 | 3e-153 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
HNJLMKBB_01183 | 6.7e-76 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
HNJLMKBB_01184 | 7e-14 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
HNJLMKBB_01185 | 1.9e-103 | S | Domain of unknown function (DUF4300) | |||
HNJLMKBB_01186 | 2e-116 | V | CAAX protease self-immunity | |||
HNJLMKBB_01187 | 5.4e-36 | 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 | |
HNJLMKBB_01188 | 1.1e-223 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
HNJLMKBB_01189 | 3.1e-113 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
HNJLMKBB_01190 | 1.6e-32 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
HNJLMKBB_01191 | 4.2e-193 | 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 | ||
HNJLMKBB_01192 | 3.4e-116 | cpsD | D | COG0489 ATPases involved in chromosome partitioning | ||
HNJLMKBB_01193 | 7.2e-65 | L | Transposase (IS116 IS110 IS902 family) | |||
HNJLMKBB_01194 | 8.4e-142 | L | PFAM transposase IS116 IS110 IS902 family | |||
HNJLMKBB_01196 | 1.7e-144 | nodB3 | G | Polysaccharide deacetylase | ||
HNJLMKBB_01197 | 2.2e-133 | S | double-stranded DNA endodeoxyribonuclease activity | |||
HNJLMKBB_01198 | 8.6e-102 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
HNJLMKBB_01199 | 1e-44 | |||||
HNJLMKBB_01200 | 3.1e-234 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
HNJLMKBB_01201 | 1e-141 | acoC | 2.3.1.12, 2.3.1.61 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
HNJLMKBB_01202 | 4.8e-16 | Q | Methyltransferase domain | |||
HNJLMKBB_01203 | 1.5e-52 | S | COG NOG10998 non supervised orthologous group | |||
HNJLMKBB_01204 | 1.2e-24 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNJLMKBB_01205 | 1e-75 | fld | C | Flavodoxin | ||
HNJLMKBB_01206 | 4.5e-15 | XK27_08880 | ||||
HNJLMKBB_01207 | 2.8e-157 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
HNJLMKBB_01208 | 4.7e-26 | |||||
HNJLMKBB_01209 | 5.5e-18 | sufB | O | assembly protein SufB | ||
HNJLMKBB_01210 | 6.5e-58 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
HNJLMKBB_01211 | 6.8e-136 | XK27_08845 | S | abc transporter atp-binding protein | ||
HNJLMKBB_01212 | 7.5e-222 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HNJLMKBB_01213 | 1.5e-26 | secE | U | SecE/Sec61-gamma subunits of protein translocation complex | ||
HNJLMKBB_01215 | 2.7e-141 | L | Transposase and inactivated derivatives | |||
HNJLMKBB_01216 | 8.1e-75 | L | Transposase | |||
HNJLMKBB_01217 | 1.3e-31 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
HNJLMKBB_01218 | 1.2e-92 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
HNJLMKBB_01219 | 1.9e-165 | pabC | 2.6.1.42, 4.1.3.38 | EH | Amino-transferase class IV | |
HNJLMKBB_01220 | 1.5e-211 | M | LPXTG-motif cell wall anchor domain protein | |||
HNJLMKBB_01221 | 2.1e-17 | yjdB | S | Domain of unknown function (DUF4767) | ||
HNJLMKBB_01222 | 6.7e-167 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
HNJLMKBB_01223 | 2.6e-58 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
HNJLMKBB_01224 | 7.2e-71 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
HNJLMKBB_01225 | 1e-44 | yktA | S | Belongs to the UPF0223 family | ||
HNJLMKBB_01226 | 1.3e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HNJLMKBB_01227 | 1.9e-133 | pyrP | F | uracil Permease | ||
HNJLMKBB_01228 | 2.9e-34 | S | Phage plasmid primase, P4 family domain protein | |||
HNJLMKBB_01229 | 3.1e-66 | 1.8.4.10, 1.8.4.8 | EH | sulfate reduction | ||
HNJLMKBB_01230 | 3e-13 | |||||
HNJLMKBB_01231 | 2.4e-17 | |||||
HNJLMKBB_01232 | 5.5e-150 | S | Terminase | |||
HNJLMKBB_01233 | 5.8e-33 | S | Phage portal protein, SPP1 Gp6-like | |||
HNJLMKBB_01234 | 5.3e-49 | |||||
HNJLMKBB_01235 | 3.6e-29 | |||||
HNJLMKBB_01236 | 7.6e-148 | S | Phage capsid family | |||
HNJLMKBB_01237 | 6.7e-13 | S | Phage protein Gp19/Gp15/Gp42 | |||
HNJLMKBB_01238 | 3.1e-36 | |||||
HNJLMKBB_01239 | 5e-47 | eae | N | domain, Protein | ||
HNJLMKBB_01242 | 2e-16 | |||||
HNJLMKBB_01244 | 4.7e-52 | NT | phage tail tape measure protein | |||
HNJLMKBB_01245 | 1.6e-149 | yitS | S | EDD domain protein, DegV family | ||
HNJLMKBB_01246 | 5.6e-107 | XK27_08075 | M | glycosyl transferase family 2 | ||
HNJLMKBB_01248 | 3.9e-54 | |||||
HNJLMKBB_01249 | 8.8e-113 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNJLMKBB_01250 | 1.4e-105 | artQ | P | ABC transporter (Permease | ||
HNJLMKBB_01251 | 6.6e-66 | ssb_2 | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
HNJLMKBB_01252 | 2.1e-45 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HNJLMKBB_01253 | 1.9e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HNJLMKBB_01254 | 2.3e-28 | V | permease protein | |||
HNJLMKBB_01255 | 5.4e-34 | M | Putative cell wall binding repeat | |||
HNJLMKBB_01256 | 3.8e-128 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
HNJLMKBB_01257 | 1.1e-166 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
HNJLMKBB_01258 | 5.4e-69 | comGF | U | Competence protein ComGF | ||
HNJLMKBB_01259 | 3.1e-15 | NU | Type II secretory pathway pseudopilin | |||
HNJLMKBB_01260 | 8.4e-70 | cglD | NU | Competence protein | ||
HNJLMKBB_01261 | 2.2e-43 | comGC | U | Required for transformation and DNA binding | ||
HNJLMKBB_01262 | 5.4e-23 | cglB | U | protein transport across the cell outer membrane | ||
HNJLMKBB_01263 | 5e-137 | ET | Belongs to the bacterial solute-binding protein 3 family | |||
HNJLMKBB_01264 | 1.6e-43 | ET | ABC transporter | |||
HNJLMKBB_01265 | 1.8e-38 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
HNJLMKBB_01266 | 8.6e-243 | clcA | P | Chloride transporter, ClC family | ||
HNJLMKBB_01268 | 1.2e-225 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
HNJLMKBB_01269 | 4.6e-17 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
HNJLMKBB_01270 | 6.6e-189 | femA | 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
HNJLMKBB_01271 | 1.2e-157 | yfjR | K | regulation of single-species biofilm formation | ||
HNJLMKBB_01272 | 4.6e-54 | corA | P | CorA-like protein | ||
HNJLMKBB_01273 | 5e-119 | sirR | K | iron dependent repressor | ||
HNJLMKBB_01274 | 5.8e-126 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HNJLMKBB_01275 | 1.5e-141 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNJLMKBB_01276 | 6.7e-93 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
HNJLMKBB_01277 | 5e-139 | L | Replication initiation factor | |||
HNJLMKBB_01278 | 2.5e-18 | S | Domain of unknown function (DUF3173) | |||
HNJLMKBB_01279 | 2.7e-85 | H | COG0463 Glycosyltransferases involved in cell wall biogenesis | |||
HNJLMKBB_01280 | 2e-33 | secG | U | Preprotein translocase subunit SecG | ||
HNJLMKBB_01281 | 6.2e-117 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HNJLMKBB_01282 | 3.7e-128 | puuD | T | peptidase C26 | ||
HNJLMKBB_01285 | 7.3e-225 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
HNJLMKBB_01286 | 1.2e-58 | rgpC | GM | Transport permease protein | ||
HNJLMKBB_01287 | 6.5e-90 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HNJLMKBB_01288 | 2.5e-83 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
HNJLMKBB_01289 | 1e-113 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
HNJLMKBB_01290 | 8e-151 | 5.2.1.8 | G | hydrolase | ||
HNJLMKBB_01291 | 1.7e-230 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
HNJLMKBB_01292 | 1.7e-196 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HNJLMKBB_01293 | 1.7e-81 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
HNJLMKBB_01294 | 9.3e-189 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
HNJLMKBB_01295 | 4e-287 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
HNJLMKBB_01296 | 1.1e-217 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
HNJLMKBB_01297 | 2.1e-104 | mur1 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | |
HNJLMKBB_01298 | 9.5e-53 | glnB | K | Belongs to the P(II) protein family | ||
HNJLMKBB_01299 | 1.8e-18 | amt | P | Ammonium Transporter | ||
HNJLMKBB_01300 | 9e-150 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
HNJLMKBB_01301 | 3.1e-101 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HNJLMKBB_01302 | 3.2e-79 | S | Bacterial inner membrane protein | |||
HNJLMKBB_01304 | 1.4e-172 | D | nuclear chromosome segregation | |||
HNJLMKBB_01305 | 1.2e-106 | G | Belongs to the phosphoglycerate mutase family | |||
HNJLMKBB_01306 | 9.7e-109 | pgm | G | Belongs to the phosphoglycerate mutase family | ||
HNJLMKBB_01307 | 5.5e-36 | supH | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | |
HNJLMKBB_01309 | 6.7e-63 | O | MreB/Mbl protein | |||
HNJLMKBB_01310 | 2.3e-107 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
HNJLMKBB_01311 | 1.3e-146 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNJLMKBB_01312 | 1.3e-105 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HNJLMKBB_01313 | 3.1e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
HNJLMKBB_01314 | 1.6e-238 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
HNJLMKBB_01315 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNJLMKBB_01316 | 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 | |
HNJLMKBB_01317 | 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 | |
HNJLMKBB_01318 | 3.8e-68 | S | cog cog4699 | |||
HNJLMKBB_01319 | 1e-38 | gcvR | T | UPF0237 protein | ||
HNJLMKBB_01320 | 3.2e-169 | capA | M | Bacterial capsule synthesis protein | ||
HNJLMKBB_01321 | 4.1e-214 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
HNJLMKBB_01322 | 6.7e-43 | yqeG | S | hydrolase of the HAD superfamily | ||
HNJLMKBB_01323 | 3.5e-153 | XK27_05675 | S | Esterase | ||
HNJLMKBB_01324 | 7.8e-105 | XK27_05670 | S | Putative esterase | ||
HNJLMKBB_01325 | 5.2e-23 | |||||
HNJLMKBB_01326 | 4.3e-124 | XK27_09800 | I | Acyltransferase | ||
HNJLMKBB_01327 | 3.5e-115 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
HNJLMKBB_01328 | 1.4e-90 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
HNJLMKBB_01329 | 2.3e-176 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HNJLMKBB_01330 | 3.5e-64 | |||||
HNJLMKBB_01331 | 2e-77 | adhB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
HNJLMKBB_01332 | 3.6e-126 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HNJLMKBB_01333 | 7.2e-10 | O | ADP-ribosylglycohydrolase | |||
HNJLMKBB_01336 | 7.4e-26 | yhaI | S | Protein of unknown function (DUF805) | ||
HNJLMKBB_01337 | 4.5e-157 | yegQ | O | Peptidase U32 | ||
HNJLMKBB_01338 | 6.3e-112 | liaI | S | membrane | ||
HNJLMKBB_01339 | 6.8e-75 | XK27_02470 | K | LytTr DNA-binding domain protein | ||
HNJLMKBB_01340 | 4.9e-54 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
HNJLMKBB_01342 | 2.9e-31 | yozG | K | Transcriptional regulator | ||
HNJLMKBB_01344 | 1.1e-43 | czrA | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
HNJLMKBB_01345 | 5.7e-119 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
HNJLMKBB_01346 | 5.6e-46 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HNJLMKBB_01347 | 1.9e-46 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HNJLMKBB_01348 | 2.5e-91 | Q | Nodulation protein S (NodS) | |||
HNJLMKBB_01349 | 1.8e-98 | XK27_07830 | 2.3.1.128 | J | Acetyltransferase GNAT Family | |
HNJLMKBB_01350 | 6.9e-50 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HNJLMKBB_01351 | 3.4e-231 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
HNJLMKBB_01352 | 6.8e-51 | XK27_01300 | P | Protein conserved in bacteria | ||
HNJLMKBB_01353 | 1.2e-106 | yfnA | E | amino acid | ||
HNJLMKBB_01354 | 9.9e-30 | liaI | KT | membrane | ||
HNJLMKBB_01355 | 6.1e-93 | XK27_05000 | S | metal cluster binding | ||
HNJLMKBB_01356 | 4.1e-29 | pspC | KT | PspC domain protein | ||
HNJLMKBB_01357 | 2.5e-200 | S | Protein of unknown function (DUF3114) | |||
HNJLMKBB_01358 | 7.2e-220 | mdtG | EGP | Major facilitator Superfamily | ||
HNJLMKBB_01359 | 2.6e-74 | ywnA | K | Transcriptional regulator | ||
HNJLMKBB_01360 | 5.9e-25 | E | Alpha/beta hydrolase of unknown function (DUF915) | |||
HNJLMKBB_01361 | 2.1e-79 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
HNJLMKBB_01362 | 1.4e-162 | pbuO | S | permease | ||
HNJLMKBB_01363 | 5.1e-119 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
HNJLMKBB_01365 | 4.8e-45 | int | L | Phage integrase family | ||
HNJLMKBB_01366 | 1.1e-89 | dps | P | Belongs to the Dps family | ||
HNJLMKBB_01367 | 3.4e-79 | perR | P | Belongs to the Fur family | ||
HNJLMKBB_01368 | 2.4e-27 | yqgQ | S | protein conserved in bacteria | ||
HNJLMKBB_01369 | 2.2e-88 | bioY | S | biotin synthase | ||
HNJLMKBB_01370 | 9.6e-97 | yegQ | O | Peptidase U32 | ||
HNJLMKBB_01371 | 2.9e-204 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HNJLMKBB_01372 | 5.3e-77 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNJLMKBB_01373 | 2.4e-74 | cpsE | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
HNJLMKBB_01374 | 7.5e-59 | |||||
HNJLMKBB_01375 | 2.5e-50 | ctpE | P | E1-E2 ATPase | ||
HNJLMKBB_01376 | 9.8e-244 | 3.2.1.26, 3.2.1.65 | GH32 | G | Belongs to the glycosyl hydrolase 32 family | |
HNJLMKBB_01377 | 2.1e-91 | XK27_05885 | 2.3.1.82 | M | phosphinothricin N-acetyltransferase activity | |
HNJLMKBB_01378 | 1.4e-291 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HNJLMKBB_01379 | 9.2e-141 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HNJLMKBB_01380 | 2.9e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HNJLMKBB_01381 | 1.4e-135 | rgpF | M | Rhamnan synthesis protein F | ||
HNJLMKBB_01382 | 9.1e-80 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HNJLMKBB_01383 | 2.8e-88 | pat | 2.3.1.183 | M | acetyltransferase | |
HNJLMKBB_01384 | 6.7e-50 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HNJLMKBB_01385 | 1.4e-47 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
HNJLMKBB_01386 | 2.2e-52 | |||||
HNJLMKBB_01388 | 8.2e-63 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
HNJLMKBB_01389 | 6.5e-45 | S | Protein of unknown function (DUF1722) | |||
HNJLMKBB_01390 | 2.6e-263 | M | Putative cell wall binding repeat | |||
HNJLMKBB_01391 | 1.7e-117 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
HNJLMKBB_01392 | 3.7e-131 | ywbD | 2.1.1.191 | J | Methyltransferase | |
HNJLMKBB_01393 | 2e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
HNJLMKBB_01394 | 2.8e-82 | 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 | |
HNJLMKBB_01395 | 1.7e-61 | yqhY | S | protein conserved in bacteria | ||
HNJLMKBB_01396 | 7.1e-98 | 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 | ||
HNJLMKBB_01397 | 2.1e-27 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HNJLMKBB_01398 | 2.2e-81 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HNJLMKBB_01399 | 8.4e-97 | manY | G | pts system | ||
HNJLMKBB_01401 | 3.3e-226 | 2.7.13.3 | T | GHKL domain | ||
HNJLMKBB_01403 | 3.2e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
HNJLMKBB_01405 | 1.1e-176 | ecsB | U | Bacterial ABC transporter protein EcsB | ||
HNJLMKBB_01406 | 4.4e-120 | XK27_00915 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
HNJLMKBB_01407 | 7.4e-65 | XK27_00915 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
HNJLMKBB_01408 | 5.7e-74 | 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 | |
HNJLMKBB_01409 | 1.5e-120 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNJLMKBB_01410 | 6.8e-21 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HNJLMKBB_01411 | 3.9e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HNJLMKBB_01412 | 5.7e-28 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
HNJLMKBB_01413 | 3.9e-198 | XK27_05680 | 6.3.2.4 | M | carbamoylphosphate synthase large subunit | |
HNJLMKBB_01414 | 3.1e-07 | |||||
HNJLMKBB_01415 | 2.2e-15 | agrA | KT | response regulator | ||
HNJLMKBB_01416 | 2e-15 | S | Domain of unknown function (DUF3173) | |||
HNJLMKBB_01417 | 2.9e-215 | int | L | Belongs to the 'phage' integrase family | ||
HNJLMKBB_01418 | 4e-146 | |||||
HNJLMKBB_01419 | 5.8e-48 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
HNJLMKBB_01420 | 3e-145 | rny | D | Endoribonuclease that initiates mRNA decay | ||
HNJLMKBB_01421 | 2.2e-146 | S | dextransucrase activity | |||
HNJLMKBB_01422 | 7.5e-89 | ttcA | 6.3.4.19 | H | Belongs to the TtcA family | |
HNJLMKBB_01423 | 2.2e-17 | hypB | H | ThiF family | ||
HNJLMKBB_01424 | 4.4e-62 | 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) | |
HNJLMKBB_01425 | 6.8e-47 | |||||
HNJLMKBB_01426 | 1.1e-32 | |||||
HNJLMKBB_01427 | 3.1e-12 | |||||
HNJLMKBB_01428 | 4.9e-39 | S | granule-associated protein | |||
HNJLMKBB_01429 | 2.9e-243 | XK27_03190 | S | hydrolases of the HAD superfamily | ||
HNJLMKBB_01431 | 7.8e-103 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
HNJLMKBB_01433 | 1.9e-46 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
HNJLMKBB_01434 | 1.2e-94 | tnp* | L | An automated process has identified a potential problem with this gene model | ||
HNJLMKBB_01435 | 2.2e-58 | dhaM | 2.7.1.121 | S | dihydroxyacetone kinase, phosphotransfer subunit | |
HNJLMKBB_01436 | 7.2e-81 | dhaL | 2.7.1.121 | S | Dihydroxyacetone kinase | |
HNJLMKBB_01437 | 1.1e-164 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
HNJLMKBB_01438 | 5.3e-130 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
HNJLMKBB_01439 | 6.8e-110 | 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 | ||
HNJLMKBB_01440 | 3.7e-60 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
HNJLMKBB_01441 | 2.9e-134 | agrA | KT | response regulator | ||
HNJLMKBB_01442 | 5e-151 | V | abc transporter atp-binding protein | |||
HNJLMKBB_01443 | 1.5e-127 | 3.6.1.13, 3.6.1.55 | F | AdP-ribose pyrophosphatase | ||
HNJLMKBB_01444 | 4.9e-90 | XK27_10930 | K | acetyltransferase | ||
HNJLMKBB_01445 | 8.2e-116 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
HNJLMKBB_01446 | 3.9e-27 | yaaA | S | Belongs to the UPF0246 family | ||
HNJLMKBB_01447 | 1.8e-80 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HNJLMKBB_01448 | 2e-97 | mip | S | hydroperoxide reductase activity | ||
HNJLMKBB_01449 | 1.6e-235 | L | Transposase | |||
HNJLMKBB_01450 | 1.5e-179 | S | Glucan-binding protein C | |||
HNJLMKBB_01451 | 2.2e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
HNJLMKBB_01452 | 3e-60 | divIC | D | Septum formation initiator | ||
HNJLMKBB_01454 | 1.3e-120 | 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 | |
HNJLMKBB_01455 | 3.1e-234 | 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 | |
HNJLMKBB_01456 | 4.6e-103 | O | protein import | |||
HNJLMKBB_01458 | 2.7e-97 | ytqB | J | (SAM)-dependent | ||
HNJLMKBB_01459 | 8.5e-49 | U | TraM recognition site of TraD and TraG | |||
HNJLMKBB_01460 | 3.2e-167 | XK27_01785 | S | cog cog1284 | ||
HNJLMKBB_01461 | 4.6e-76 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
HNJLMKBB_01462 | 2.9e-74 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
HNJLMKBB_01463 | 1.6e-12 | S | dextransucrase activity | |||
HNJLMKBB_01464 | 2.7e-230 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
HNJLMKBB_01465 | 3.1e-47 | macB | V | ABC transporter, ATP-binding protein | ||
HNJLMKBB_01466 | 1.8e-105 | K | Bacterial regulatory proteins, tetR family | |||
HNJLMKBB_01467 | 2.1e-84 | ybhR | V | ABC transporter | ||
HNJLMKBB_01468 | 9.1e-261 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
HNJLMKBB_01469 | 1.9e-92 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
HNJLMKBB_01471 | 1.2e-61 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
HNJLMKBB_01472 | 6.3e-82 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
HNJLMKBB_01473 | 4e-81 | XK27_10720 | D | peptidase activity | ||
HNJLMKBB_01474 | 1.7e-122 | pepD | E | Dipeptidase | ||
HNJLMKBB_01475 | 1.1e-127 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HNJLMKBB_01476 | 2.6e-43 | S | VIT family | |||
HNJLMKBB_01477 | 2.7e-205 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
HNJLMKBB_01478 | 6.7e-151 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
HNJLMKBB_01479 | 3e-34 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HNJLMKBB_01480 | 2.2e-92 | 2.7.7.65 | T | Psort location CytoplasmicMembrane, score | ||
HNJLMKBB_01481 | 9.6e-87 | V | Glucan-binding protein C | |||
HNJLMKBB_01482 | 2.2e-177 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HNJLMKBB_01485 | 2.2e-70 | yocS | S | Transporter | ||
HNJLMKBB_01486 | 2.8e-97 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
HNJLMKBB_01487 | 9.7e-236 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
HNJLMKBB_01488 | 3e-147 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
HNJLMKBB_01490 | 7.2e-68 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
HNJLMKBB_01493 | 1.1e-144 | 6.2.1.30 | H | Coenzyme F390 synthetase | ||
HNJLMKBB_01494 | 2.4e-86 | oppA | E | ABC transporter substrate-binding protein | ||
HNJLMKBB_01495 | 1.3e-153 | uup | S | abc transporter atp-binding protein | ||
HNJLMKBB_01496 | 6.8e-15 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
HNJLMKBB_01497 | 8.4e-23 | K | sequence-specific DNA binding | |||
HNJLMKBB_01498 | 4.7e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
HNJLMKBB_01499 | 7.8e-138 | S | membrane | |||
HNJLMKBB_01500 | 1.8e-25 | |||||
HNJLMKBB_01502 | 2.1e-76 | S | MvaI/BcnI restriction endonuclease family | |||
HNJLMKBB_01503 | 2.3e-170 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HNJLMKBB_01504 | 1.1e-161 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
HNJLMKBB_01505 | 7.2e-77 | G | protein with an alpha beta hydrolase fold | |||
HNJLMKBB_01506 | 2.8e-79 | V | ABC transporter | |||
HNJLMKBB_01507 | 1.5e-119 | sagI | S | ABC-2 type transporter | ||
HNJLMKBB_01508 | 1.4e-84 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HNJLMKBB_01509 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
HNJLMKBB_01510 | 1e-246 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HNJLMKBB_01511 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
HNJLMKBB_01512 | 5.8e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
HNJLMKBB_01513 | 3.2e-10 | |||||
HNJLMKBB_01514 | 4.5e-53 | ypaA | M | Membrane | ||
HNJLMKBB_01515 | 7.1e-95 | XK27_06935 | K | transcriptional regulator | ||
HNJLMKBB_01516 | 1.6e-159 | XK27_06930 | V | domain protein | ||
HNJLMKBB_01517 | 1.4e-108 | S | Putative adhesin | |||
HNJLMKBB_01518 | 8.6e-62 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
HNJLMKBB_01519 | 6.3e-54 | K | transcriptional regulator, PadR family | |||
HNJLMKBB_01520 | 2.2e-116 | nudL | L | hydrolase | ||
HNJLMKBB_01521 | 3.1e-198 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
HNJLMKBB_01522 | 1e-115 | manL | 2.7.1.191 | G | pts system | |
HNJLMKBB_01523 | 1.5e-29 | K | Helix-turn-helix domain | |||
HNJLMKBB_01524 | 6.2e-20 | |||||
HNJLMKBB_01525 | 8.5e-218 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
HNJLMKBB_01526 | 3.9e-215 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
HNJLMKBB_01527 | 3.7e-154 | lmrA | V | abc transporter atp-binding protein | ||
HNJLMKBB_01528 | 4.6e-48 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
HNJLMKBB_01529 | 2.3e-162 | yxeN | P | ABC transporter (Permease | ||
HNJLMKBB_01531 | 7.1e-74 | norM | V | Multidrug efflux pump | ||
HNJLMKBB_01532 | 1.1e-73 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HNJLMKBB_01533 | 7.7e-33 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
HNJLMKBB_01534 | 1.2e-103 | U | COG COG3505 Type IV secretory pathway, VirD4 components | |||
HNJLMKBB_01535 | 5.7e-118 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HNJLMKBB_01536 | 8.3e-73 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
HNJLMKBB_01537 | 1.8e-33 | XK27_12190 | S | protein conserved in bacteria | ||
HNJLMKBB_01539 | 1.1e-111 | ytmL | P | ABC transporter (Permease | ||
HNJLMKBB_01540 | 2.5e-55 | ET | ABC transporter substrate-binding protein | |||
HNJLMKBB_01541 | 1.1e-131 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
HNJLMKBB_01542 | 3.2e-208 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
HNJLMKBB_01544 | 4.9e-07 | S | Protein of unknown function (DUF3169) | |||
HNJLMKBB_01545 | 5.5e-27 | XK27_07105 | K | transcriptional | ||
HNJLMKBB_01546 | 5.8e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HNJLMKBB_01547 | 2.7e-146 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
HNJLMKBB_01548 | 7.1e-19 | pgpB | 3.6.1.27 | I | phosphatidate phosphatase activity | |
HNJLMKBB_01549 | 8.8e-68 | tdk | 2.7.1.21 | F | thymidine kinase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)