ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HCMCPFGN_00001 | 4.1e-256 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
HCMCPFGN_00002 | 3.9e-196 | 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 | |
HCMCPFGN_00003 | 1.7e-34 | yaaA | S | S4 domain protein YaaA | ||
HCMCPFGN_00004 | 9e-209 | 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 | ||
HCMCPFGN_00005 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
HCMCPFGN_00006 | 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 | |
HCMCPFGN_00007 | 4.2e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HCMCPFGN_00008 | 9e-79 | 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 | ||
HCMCPFGN_00009 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
HCMCPFGN_00010 | 2.2e-154 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_00011 | 2.8e-48 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_00012 | 7.7e-227 | L | Transposase | |||
HCMCPFGN_00013 | 9.2e-175 | V | ABC transporter transmembrane region | |||
HCMCPFGN_00014 | 1e-31 | KLT | serine threonine protein kinase | |||
HCMCPFGN_00015 | 3.7e-48 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_00017 | 9.4e-112 | S | SLAP domain | |||
HCMCPFGN_00018 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HCMCPFGN_00019 | 1.1e-67 | rplI | J | Binds to the 23S rRNA | ||
HCMCPFGN_00020 | 6.7e-254 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
HCMCPFGN_00021 | 3.3e-164 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
HCMCPFGN_00022 | 5.1e-173 | degV | S | DegV family | ||
HCMCPFGN_00023 | 9.3e-169 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
HCMCPFGN_00024 | 1.7e-38 | L | Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_00025 | 4.5e-76 | L | Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_00026 | 4.6e-263 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00028 | 4.7e-36 | |||||
HCMCPFGN_00029 | 2.8e-240 | I | Protein of unknown function (DUF2974) | |||
HCMCPFGN_00030 | 5.4e-119 | yhiD | S | MgtC family | ||
HCMCPFGN_00033 | 2.9e-83 | |||||
HCMCPFGN_00034 | 4.8e-21 | D | Ftsk spoiiie family protein | |||
HCMCPFGN_00035 | 7e-107 | D | Ftsk spoiiie family protein | |||
HCMCPFGN_00036 | 2e-82 | S | Replication initiation factor | |||
HCMCPFGN_00037 | 2.5e-41 | |||||
HCMCPFGN_00038 | 8.2e-27 | |||||
HCMCPFGN_00039 | 3.9e-166 | L | Belongs to the 'phage' integrase family | |||
HCMCPFGN_00040 | 3.3e-25 | sufS | 2.8.1.7, 4.4.1.16 | E | PFAM aminotransferase class V | |
HCMCPFGN_00041 | 3.3e-36 | sufS | 2.8.1.7, 4.4.1.16 | E | PFAM aminotransferase class V | |
HCMCPFGN_00042 | 2e-67 | 3.6.1.17 | FG | bis(5'-adenosyl)-triphosphatase activity | ||
HCMCPFGN_00043 | 1.6e-22 | I | bis(5'-adenosyl)-triphosphatase activity | |||
HCMCPFGN_00044 | 4.2e-68 | S | EamA-like transporter family | |||
HCMCPFGN_00045 | 4.2e-247 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00046 | 2.6e-244 | eno2 | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
HCMCPFGN_00048 | 3.9e-30 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
HCMCPFGN_00049 | 1.2e-112 | ybbL | S | ABC transporter, ATP-binding protein | ||
HCMCPFGN_00050 | 4.3e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
HCMCPFGN_00051 | 5.5e-192 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00052 | 2.4e-140 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HCMCPFGN_00053 | 8e-24 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HCMCPFGN_00054 | 3.7e-105 | K | Bacterial regulatory proteins, tetR family | |||
HCMCPFGN_00055 | 9.8e-116 | V | Restriction endonuclease | |||
HCMCPFGN_00056 | 1.4e-144 | L | Transposase IS66 family | |||
HCMCPFGN_00057 | 2.9e-31 | S | Transposase C of IS166 homeodomain | |||
HCMCPFGN_00058 | 2.5e-64 | XK27_01125 | L | IS66 Orf2 like protein | ||
HCMCPFGN_00059 | 1.8e-18 | |||||
HCMCPFGN_00060 | 3e-90 | V | Restriction endonuclease | |||
HCMCPFGN_00061 | 2.5e-59 | pipD | E | Dipeptidase | ||
HCMCPFGN_00062 | 1.1e-232 | S | LPXTG cell wall anchor motif | |||
HCMCPFGN_00063 | 6.1e-148 | S | Putative ABC-transporter type IV | |||
HCMCPFGN_00064 | 2.5e-98 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
HCMCPFGN_00065 | 1.7e-85 | S | ECF transporter, substrate-specific component | |||
HCMCPFGN_00066 | 2.1e-59 | S | Domain of unknown function (DUF4430) | |||
HCMCPFGN_00067 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
HCMCPFGN_00068 | 2.3e-174 | K | AI-2E family transporter | |||
HCMCPFGN_00069 | 6.8e-104 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
HCMCPFGN_00070 | 1.3e-11 | |||||
HCMCPFGN_00071 | 3.2e-51 | |||||
HCMCPFGN_00072 | 9.6e-138 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
HCMCPFGN_00073 | 2.2e-125 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
HCMCPFGN_00074 | 8e-177 | ABC-SBP | S | ABC transporter | ||
HCMCPFGN_00075 | 9.2e-135 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
HCMCPFGN_00076 | 1.7e-15 | S | Bacteriocin helveticin-J | |||
HCMCPFGN_00077 | 1.1e-211 | S | SLAP domain | |||
HCMCPFGN_00078 | 3e-164 | yvgN | C | Aldo keto reductase | ||
HCMCPFGN_00079 | 0.0 | tetP | J | elongation factor G | ||
HCMCPFGN_00080 | 7.9e-154 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | haloacid dehalogenase-like hydrolase | ||
HCMCPFGN_00081 | 5.1e-269 | nisT | V | ABC transporter | ||
HCMCPFGN_00082 | 6.4e-46 | |||||
HCMCPFGN_00083 | 3.3e-56 | |||||
HCMCPFGN_00084 | 3.4e-191 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_00085 | 8.9e-68 | yniA | G | Phosphotransferase enzyme family | ||
HCMCPFGN_00086 | 4.1e-92 | yniA | G | Phosphotransferase enzyme family | ||
HCMCPFGN_00087 | 3.3e-160 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HCMCPFGN_00088 | 1.4e-262 | E | amino acid | |||
HCMCPFGN_00089 | 0.0 | L | Helicase C-terminal domain protein | |||
HCMCPFGN_00090 | 4.3e-194 | pbpX1 | V | Beta-lactamase | ||
HCMCPFGN_00091 | 3e-69 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
HCMCPFGN_00092 | 6.5e-77 | |||||
HCMCPFGN_00093 | 2.4e-83 | S | COG NOG38524 non supervised orthologous group | |||
HCMCPFGN_00095 | 2.6e-41 | K | LysR substrate binding domain | |||
HCMCPFGN_00096 | 2.7e-100 | K | LysR substrate binding domain | |||
HCMCPFGN_00097 | 6.3e-105 | K | Transcriptional regulator, LysR family | |||
HCMCPFGN_00098 | 2.1e-18 | S | Cytochrome b5 | |||
HCMCPFGN_00099 | 7.3e-166 | arbZ | I | Phosphate acyltransferases | ||
HCMCPFGN_00100 | 5.3e-162 | arbY | M | Glycosyl transferase family 8 | ||
HCMCPFGN_00101 | 2.6e-185 | arbY | M | Glycosyl transferase family 8 | ||
HCMCPFGN_00102 | 1.7e-143 | arbx | M | Glycosyl transferase family 8 | ||
HCMCPFGN_00103 | 5.3e-128 | arbV | 2.3.1.51 | I | Acyl-transferase | |
HCMCPFGN_00104 | 3.5e-219 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00105 | 1.2e-202 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_00106 | 3.2e-222 | V | ABC-type multidrug transport system, ATPase and permease components | |||
HCMCPFGN_00108 | 1.4e-33 | |||||
HCMCPFGN_00110 | 2.2e-131 | K | response regulator | |||
HCMCPFGN_00111 | 2e-306 | vicK | 2.7.13.3 | T | Histidine kinase | |
HCMCPFGN_00112 | 6.7e-243 | yycH | S | YycH protein | ||
HCMCPFGN_00113 | 2.7e-146 | yycI | S | YycH protein | ||
HCMCPFGN_00114 | 3.3e-149 | vicX | 3.1.26.11 | S | domain protein | |
HCMCPFGN_00115 | 2.2e-179 | htrA | 3.4.21.107 | O | serine protease | |
HCMCPFGN_00116 | 1.6e-90 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HCMCPFGN_00117 | 5.6e-38 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_00118 | 8.8e-25 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_00120 | 3.9e-82 | V | ABC transporter | |||
HCMCPFGN_00121 | 9.2e-40 | |||||
HCMCPFGN_00122 | 5.6e-30 | higA | K | Helix-turn-helix XRE-family like proteins | ||
HCMCPFGN_00123 | 6.3e-173 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
HCMCPFGN_00124 | 1.3e-90 | P | Cobalt transport protein | |||
HCMCPFGN_00125 | 1.4e-245 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
HCMCPFGN_00126 | 1.9e-172 | K | helix_turn_helix, arabinose operon control protein | |||
HCMCPFGN_00127 | 7e-37 | L | hmm pf00665 | |||
HCMCPFGN_00128 | 2.3e-36 | L | hmm pf00665 | |||
HCMCPFGN_00129 | 1.3e-60 | L | hmm pf00665 | |||
HCMCPFGN_00130 | 2.7e-113 | L | Helix-turn-helix domain | |||
HCMCPFGN_00131 | 3.9e-162 | htpX | O | Belongs to the peptidase M48B family | ||
HCMCPFGN_00132 | 2.3e-96 | lemA | S | LemA family | ||
HCMCPFGN_00133 | 9.8e-192 | ybiR | P | Citrate transporter | ||
HCMCPFGN_00134 | 7.7e-70 | S | Iron-sulphur cluster biosynthesis | |||
HCMCPFGN_00135 | 1e-60 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
HCMCPFGN_00136 | 1.3e-45 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
HCMCPFGN_00137 | 8.5e-162 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
HCMCPFGN_00138 | 1.2e-17 | |||||
HCMCPFGN_00139 | 2.4e-121 | yfbR | S | HD containing hydrolase-like enzyme | ||
HCMCPFGN_00140 | 6.3e-162 | L | HNH nucleases | |||
HCMCPFGN_00141 | 8.1e-137 | glnQ | E | ABC transporter, ATP-binding protein | ||
HCMCPFGN_00142 | 4.1e-287 | glnP | P | ABC transporter permease | ||
HCMCPFGN_00143 | 1.5e-120 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
HCMCPFGN_00144 | 1.8e-62 | yeaO | S | Protein of unknown function, DUF488 | ||
HCMCPFGN_00145 | 2.5e-120 | terC | P | Integral membrane protein TerC family | ||
HCMCPFGN_00146 | 3.5e-91 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
HCMCPFGN_00147 | 4e-130 | cobB | K | SIR2 family | ||
HCMCPFGN_00148 | 3.5e-85 | |||||
HCMCPFGN_00149 | 4.9e-284 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HCMCPFGN_00150 | 6.8e-178 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HCMCPFGN_00151 | 2.1e-145 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HCMCPFGN_00152 | 2.4e-138 | ypuA | S | Protein of unknown function (DUF1002) | ||
HCMCPFGN_00153 | 1.2e-159 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
HCMCPFGN_00154 | 5.6e-126 | S | Alpha/beta hydrolase family | |||
HCMCPFGN_00155 | 1.5e-115 | GM | NmrA-like family | |||
HCMCPFGN_00156 | 2.5e-55 | |||||
HCMCPFGN_00157 | 1.4e-181 | 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) | |
HCMCPFGN_00158 | 8.7e-122 | luxT | K | Bacterial regulatory proteins, tetR family | ||
HCMCPFGN_00159 | 1e-129 | |||||
HCMCPFGN_00160 | 1e-260 | glnPH2 | P | ABC transporter permease | ||
HCMCPFGN_00161 | 1.1e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HCMCPFGN_00162 | 3.2e-231 | S | Cysteine-rich secretory protein family | |||
HCMCPFGN_00163 | 2.4e-206 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HCMCPFGN_00164 | 2.2e-94 | |||||
HCMCPFGN_00165 | 5.9e-200 | yibE | S | overlaps another CDS with the same product name | ||
HCMCPFGN_00166 | 2.2e-129 | yibF | S | overlaps another CDS with the same product name | ||
HCMCPFGN_00167 | 3.8e-156 | I | alpha/beta hydrolase fold | |||
HCMCPFGN_00168 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
HCMCPFGN_00169 | 5.7e-80 | ntd | 2.4.2.6 | F | Nucleoside | |
HCMCPFGN_00170 | 5.6e-86 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
HCMCPFGN_00171 | 1.4e-147 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
HCMCPFGN_00172 | 5.5e-86 | uspA | T | universal stress protein | ||
HCMCPFGN_00174 | 3.2e-151 | phnD | P | Phosphonate ABC transporter | ||
HCMCPFGN_00175 | 5.7e-138 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
HCMCPFGN_00176 | 1.6e-127 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
HCMCPFGN_00177 | 4.6e-146 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
HCMCPFGN_00178 | 1.3e-243 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00179 | 7.8e-108 | tag | 3.2.2.20 | L | glycosylase | |
HCMCPFGN_00180 | 1.1e-81 | |||||
HCMCPFGN_00181 | 1.1e-272 | S | Calcineurin-like phosphoesterase | |||
HCMCPFGN_00182 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
HCMCPFGN_00183 | 1.4e-253 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
HCMCPFGN_00186 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HCMCPFGN_00187 | 4.3e-140 | 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 | |
HCMCPFGN_00188 | 7.8e-100 | S | Iron-sulfur cluster assembly protein | |||
HCMCPFGN_00189 | 7.5e-230 | XK27_04775 | S | PAS domain | ||
HCMCPFGN_00190 | 5.7e-225 | yttB | EGP | Major facilitator Superfamily | ||
HCMCPFGN_00191 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HCMCPFGN_00192 | 0.0 | kup | P | Transport of potassium into the cell | ||
HCMCPFGN_00193 | 3.8e-71 | |||||
HCMCPFGN_00195 | 1e-28 | |||||
HCMCPFGN_00196 | 1.3e-36 | S | Protein of unknown function (DUF2922) | |||
HCMCPFGN_00197 | 3.8e-166 | S | SLAP domain | |||
HCMCPFGN_00199 | 5.4e-12 | K | DNA-templated transcription, initiation | |||
HCMCPFGN_00200 | 7.1e-26 | K | DNA-templated transcription, initiation | |||
HCMCPFGN_00201 | 2.4e-97 | |||||
HCMCPFGN_00202 | 1.1e-223 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
HCMCPFGN_00203 | 1.3e-209 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
HCMCPFGN_00204 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
HCMCPFGN_00205 | 1.1e-24 | gepA | K | Protein of unknown function (DUF4065) | ||
HCMCPFGN_00206 | 7.4e-93 | gepA | K | Protein of unknown function (DUF4065) | ||
HCMCPFGN_00207 | 4.1e-267 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00208 | 1.4e-178 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
HCMCPFGN_00209 | 1.5e-46 | |||||
HCMCPFGN_00210 | 3.4e-206 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00211 | 1.3e-52 | |||||
HCMCPFGN_00212 | 1.1e-133 | |||||
HCMCPFGN_00213 | 1.9e-132 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HCMCPFGN_00214 | 7.4e-109 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
HCMCPFGN_00215 | 5.3e-101 | G | Aldose 1-epimerase | |||
HCMCPFGN_00216 | 8e-202 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HCMCPFGN_00217 | 6.2e-111 | plsY | 2.3.1.15 | 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 | |
HCMCPFGN_00218 | 0.0 | XK27_08315 | M | Sulfatase | ||
HCMCPFGN_00219 | 4.9e-265 | S | Fibronectin type III domain | |||
HCMCPFGN_00220 | 9.7e-244 | 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) | |
HCMCPFGN_00221 | 5.4e-21 | |||||
HCMCPFGN_00223 | 3e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
HCMCPFGN_00224 | 2.1e-117 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HCMCPFGN_00225 | 1.1e-209 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
HCMCPFGN_00226 | 2.6e-255 | pepC | 3.4.22.40 | E | aminopeptidase | |
HCMCPFGN_00227 | 2.6e-68 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
HCMCPFGN_00228 | 1.8e-75 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
HCMCPFGN_00229 | 4.9e-114 | |||||
HCMCPFGN_00231 | 4.5e-114 | E | Belongs to the SOS response-associated peptidase family | |||
HCMCPFGN_00232 | 1.1e-192 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HCMCPFGN_00233 | 5.5e-91 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
HCMCPFGN_00234 | 4.6e-109 | S | TPM domain | |||
HCMCPFGN_00235 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
HCMCPFGN_00236 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
HCMCPFGN_00237 | 4.3e-146 | tatD | L | hydrolase, TatD family | ||
HCMCPFGN_00238 | 1.9e-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 | |
HCMCPFGN_00239 | 2.1e-160 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
HCMCPFGN_00240 | 2.7e-263 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00241 | 5e-38 | veg | S | Biofilm formation stimulator VEG | ||
HCMCPFGN_00242 | 2.2e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
HCMCPFGN_00243 | 6.1e-191 | 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 | |
HCMCPFGN_00244 | 2.5e-93 | S | SLAP domain | |||
HCMCPFGN_00245 | 8.3e-163 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00246 | 1.9e-205 | S | SLAP domain | |||
HCMCPFGN_00247 | 2.3e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
HCMCPFGN_00248 | 6.5e-149 | GK | ROK family | |||
HCMCPFGN_00249 | 5.5e-43 | |||||
HCMCPFGN_00250 | 4.7e-268 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HCMCPFGN_00251 | 3.6e-67 | S | Domain of unknown function (DUF1934) | |||
HCMCPFGN_00252 | 1.5e-47 | 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 | ||
HCMCPFGN_00253 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
HCMCPFGN_00254 | 8.1e-246 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
HCMCPFGN_00255 | 3.7e-33 | S | Haloacid dehalogenase-like hydrolase | |||
HCMCPFGN_00256 | 4.4e-49 | S | Haloacid dehalogenase-like hydrolase | |||
HCMCPFGN_00257 | 1.7e-284 | pipD | E | Dipeptidase | ||
HCMCPFGN_00258 | 5.3e-158 | msmR | K | AraC-like ligand binding domain | ||
HCMCPFGN_00259 | 4.9e-219 | pbuX | F | xanthine permease | ||
HCMCPFGN_00260 | 7.4e-98 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
HCMCPFGN_00261 | 2e-111 | K | DNA-binding helix-turn-helix protein | |||
HCMCPFGN_00262 | 4.7e-21 | K | Helix-turn-helix | |||
HCMCPFGN_00263 | 4.9e-17 | K | Helix-turn-helix | |||
HCMCPFGN_00264 | 1e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
HCMCPFGN_00265 | 1.1e-95 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_00266 | 1.4e-11 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00267 | 2.2e-191 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00268 | 1.2e-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 | |
HCMCPFGN_00269 | 3.8e-45 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00270 | 1.2e-88 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00271 | 4.1e-14 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_00272 | 1.2e-25 | L | Transposase | |||
HCMCPFGN_00273 | 2.1e-67 | L | Transposase | |||
HCMCPFGN_00274 | 5.5e-68 | L | Transposase | |||
HCMCPFGN_00275 | 1.3e-159 | |||||
HCMCPFGN_00276 | 2.2e-226 | L | Transposase | |||
HCMCPFGN_00277 | 1.2e-16 | S | Bacteriocin helveticin-J | |||
HCMCPFGN_00278 | 1.2e-135 | S | Bacteriocin helveticin-J | |||
HCMCPFGN_00279 | 3.8e-185 | S | SLAP domain | |||
HCMCPFGN_00280 | 2.7e-219 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00281 | 1.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HCMCPFGN_00282 | 1.3e-38 | rpmE2 | J | Ribosomal protein L31 | ||
HCMCPFGN_00283 | 1e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
HCMCPFGN_00284 | 5.5e-246 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
HCMCPFGN_00285 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
HCMCPFGN_00286 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HCMCPFGN_00287 | 2.9e-92 | K | transcriptional regulator | |||
HCMCPFGN_00288 | 2.4e-127 | S | (CBS) domain | |||
HCMCPFGN_00289 | 7.3e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HCMCPFGN_00290 | 3.3e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
HCMCPFGN_00291 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
HCMCPFGN_00292 | 1.8e-34 | yabO | J | S4 domain protein | ||
HCMCPFGN_00293 | 5.8e-59 | divIC | D | Septum formation initiator | ||
HCMCPFGN_00294 | 2.2e-60 | yabR | J | S1 RNA binding domain | ||
HCMCPFGN_00295 | 1.2e-241 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
HCMCPFGN_00296 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
HCMCPFGN_00297 | 5e-162 | 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 | ||
HCMCPFGN_00298 | 1e-195 | 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 | ||
HCMCPFGN_00299 | 1.3e-298 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
HCMCPFGN_00301 | 5.7e-28 | |||||
HCMCPFGN_00302 | 1.6e-08 | |||||
HCMCPFGN_00304 | 2.9e-81 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
HCMCPFGN_00305 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
HCMCPFGN_00306 | 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 | |
HCMCPFGN_00307 | 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 | |
HCMCPFGN_00308 | 2.4e-65 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_00309 | 1.5e-155 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_00310 | 2.3e-122 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
HCMCPFGN_00311 | 7.8e-70 | 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 | ||
HCMCPFGN_00312 | 2.3e-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 | ||
HCMCPFGN_00313 | 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 | ||
HCMCPFGN_00314 | 6.4e-233 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_00315 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HCMCPFGN_00316 | 6.9e-113 | 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 | ||
HCMCPFGN_00317 | 2.3e-105 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HCMCPFGN_00318 | 4.1e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HCMCPFGN_00319 | 4.7e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
HCMCPFGN_00320 | 9.3e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HCMCPFGN_00321 | 4e-54 | 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 | ||
HCMCPFGN_00322 | 5.4e-108 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HCMCPFGN_00323 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HCMCPFGN_00324 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HCMCPFGN_00325 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HCMCPFGN_00326 | 1.5e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HCMCPFGN_00327 | 1.7e-32 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HCMCPFGN_00328 | 3.6e-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 | ||
HCMCPFGN_00329 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
HCMCPFGN_00330 | 7.2e-68 | 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 | ||
HCMCPFGN_00331 | 9.5e-92 | 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 | ||
HCMCPFGN_00332 | 2.8e-55 | 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 | ||
HCMCPFGN_00333 | 1.8e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HCMCPFGN_00334 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
HCMCPFGN_00335 | 1.5e-71 | rplO | J | Binds to the 23S rRNA | ||
HCMCPFGN_00336 | 4e-237 | 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 | ||
HCMCPFGN_00337 | 2.7e-120 | 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 | |
HCMCPFGN_00338 | 8.4e-34 | 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 | ||
HCMCPFGN_00339 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
HCMCPFGN_00340 | 4.2e-56 | 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 | ||
HCMCPFGN_00341 | 3e-63 | 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 | ||
HCMCPFGN_00342 | 1.8e-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 | |
HCMCPFGN_00343 | 4e-60 | rplQ | J | Ribosomal protein L17 | ||
HCMCPFGN_00344 | 1.7e-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 | ||
HCMCPFGN_00345 | 4e-150 | ecfA | 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 | |
HCMCPFGN_00346 | 1.8e-139 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
HCMCPFGN_00347 | 1.7e-142 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
HCMCPFGN_00348 | 1.3e-78 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HCMCPFGN_00349 | 7.9e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HCMCPFGN_00350 | 5.5e-47 | S | Protein of unknown function (DUF805) | |||
HCMCPFGN_00351 | 3e-107 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
HCMCPFGN_00352 | 2.7e-112 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
HCMCPFGN_00353 | 1.9e-133 | S | membrane transporter protein | |||
HCMCPFGN_00354 | 2e-126 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
HCMCPFGN_00355 | 6e-163 | czcD | P | cation diffusion facilitator family transporter | ||
HCMCPFGN_00356 | 5.5e-23 | |||||
HCMCPFGN_00357 | 8.3e-125 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
HCMCPFGN_00358 | 1.6e-182 | S | AAA domain | |||
HCMCPFGN_00359 | 6.2e-105 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00360 | 2.1e-114 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00361 | 0.0 | mgtA | 3.6.3.2, 3.6.3.6 | P | COG0474 Cation transport ATPase | |
HCMCPFGN_00362 | 2.3e-09 | |||||
HCMCPFGN_00363 | 1.1e-145 | glcU | U | sugar transport | ||
HCMCPFGN_00364 | 3.6e-265 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HCMCPFGN_00365 | 2.5e-141 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_00366 | 5.4e-204 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00367 | 4.5e-54 | |||||
HCMCPFGN_00368 | 9.5e-103 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
HCMCPFGN_00369 | 1.2e-255 | 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 | ||
HCMCPFGN_00370 | 1.5e-291 | 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) | |
HCMCPFGN_00371 | 3.5e-274 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HCMCPFGN_00372 | 7.9e-76 | 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) | ||
HCMCPFGN_00373 | 7.8e-140 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HCMCPFGN_00374 | 2.7e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
HCMCPFGN_00375 | 8.3e-34 | |||||
HCMCPFGN_00376 | 1.3e-282 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
HCMCPFGN_00377 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
HCMCPFGN_00378 | 5.9e-24 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
HCMCPFGN_00379 | 6.9e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
HCMCPFGN_00380 | 6.9e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
HCMCPFGN_00381 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
HCMCPFGN_00382 | 1.4e-156 | pstS | P | Phosphate | ||
HCMCPFGN_00383 | 1.9e-173 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
HCMCPFGN_00384 | 7.7e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
HCMCPFGN_00385 | 9.3e-144 | 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 | |
HCMCPFGN_00386 | 7.8e-140 | 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 | |
HCMCPFGN_00387 | 7.5e-118 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
HCMCPFGN_00388 | 4.1e-10 | yfdV | S | Membrane transport protein | ||
HCMCPFGN_00389 | 4.8e-155 | yfdV | S | Membrane transport protein | ||
HCMCPFGN_00390 | 3.5e-83 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HCMCPFGN_00391 | 2.2e-52 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HCMCPFGN_00392 | 4.9e-36 | rsmC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
HCMCPFGN_00393 | 1.4e-83 | rsmC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
HCMCPFGN_00394 | 7.7e-117 | rsmC | 2.1.1.172 | J | Methyltransferase | |
HCMCPFGN_00395 | 6.9e-92 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HCMCPFGN_00396 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HCMCPFGN_00397 | 5e-38 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
HCMCPFGN_00398 | 1.6e-108 | 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 | ||
HCMCPFGN_00399 | 2.6e-33 | S | Protein of unknown function (DUF2508) | |||
HCMCPFGN_00400 | 1.9e-115 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
HCMCPFGN_00401 | 6.4e-51 | yaaQ | S | Cyclic-di-AMP receptor | ||
HCMCPFGN_00402 | 1.7e-154 | holB | 2.7.7.7 | L | DNA polymerase III | |
HCMCPFGN_00403 | 4.5e-58 | yabA | L | Involved in initiation control of chromosome replication | ||
HCMCPFGN_00404 | 5.7e-155 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HCMCPFGN_00405 | 7.3e-143 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
HCMCPFGN_00406 | 2e-86 | S | ECF transporter, substrate-specific component | |||
HCMCPFGN_00407 | 5e-131 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
HCMCPFGN_00408 | 1.7e-102 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
HCMCPFGN_00409 | 3.1e-195 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
HCMCPFGN_00410 | 3.3e-124 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
HCMCPFGN_00411 | 1.4e-181 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
HCMCPFGN_00412 | 2e-129 | K | UTRA | |||
HCMCPFGN_00413 | 4.1e-28 | S | Toxin ToxN, type III toxin-antitoxin system | |||
HCMCPFGN_00414 | 1.1e-43 | yfdE | 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HCMCPFGN_00415 | 5e-54 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HCMCPFGN_00416 | 9e-108 | yfdE | 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HCMCPFGN_00417 | 1.1e-113 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
HCMCPFGN_00418 | 8.6e-38 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
HCMCPFGN_00419 | 1.4e-216 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
HCMCPFGN_00420 | 1.4e-12 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
HCMCPFGN_00421 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
HCMCPFGN_00422 | 5.7e-116 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
HCMCPFGN_00423 | 9.6e-77 | XK27_02470 | K | LytTr DNA-binding domain | ||
HCMCPFGN_00424 | 2.5e-122 | liaI | S | membrane | ||
HCMCPFGN_00425 | 3.1e-181 | scrR | K | Transcriptional regulator, LacI family | ||
HCMCPFGN_00426 | 3.2e-230 | scrB | 3.2.1.26 | GH32 | G | invertase |
HCMCPFGN_00427 | 0.0 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
HCMCPFGN_00428 | 3.9e-47 | |||||
HCMCPFGN_00429 | 1.6e-88 | |||||
HCMCPFGN_00430 | 3e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HCMCPFGN_00431 | 9.4e-292 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
HCMCPFGN_00432 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HCMCPFGN_00433 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
HCMCPFGN_00434 | 4.6e-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 | |
HCMCPFGN_00435 | 2.8e-185 | 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 | |
HCMCPFGN_00436 | 2.9e-35 | yajC | U | Preprotein translocase | ||
HCMCPFGN_00437 | 5.4e-283 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
HCMCPFGN_00438 | 1.3e-210 | 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 | |
HCMCPFGN_00439 | 3e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
HCMCPFGN_00440 | 4.4e-226 | 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 | |
HCMCPFGN_00441 | 7.1e-64 | |||||
HCMCPFGN_00442 | 1.2e-85 | |||||
HCMCPFGN_00443 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
HCMCPFGN_00444 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
HCMCPFGN_00445 | 1e-72 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HCMCPFGN_00446 | 1.4e-50 | yrzB | S | Belongs to the UPF0473 family | ||
HCMCPFGN_00447 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
HCMCPFGN_00448 | 4.6e-54 | trxA | O | Belongs to the thioredoxin family | ||
HCMCPFGN_00449 | 8.4e-39 | 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 | ||
HCMCPFGN_00450 | 8.5e-69 | yslB | S | Protein of unknown function (DUF2507) | ||
HCMCPFGN_00451 | 7.7e-146 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HCMCPFGN_00452 | 7.1e-115 | 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 | |
HCMCPFGN_00453 | 4.6e-149 | ykuT | M | mechanosensitive ion channel | ||
HCMCPFGN_00454 | 3.3e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
HCMCPFGN_00455 | 2.6e-43 | |||||
HCMCPFGN_00456 | 2.2e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HCMCPFGN_00457 | 1.1e-178 | ccpA | K | catabolite control protein A | ||
HCMCPFGN_00458 | 1.1e-254 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
HCMCPFGN_00459 | 1.1e-55 | |||||
HCMCPFGN_00460 | 2.5e-277 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
HCMCPFGN_00461 | 3.1e-86 | yutD | S | Protein of unknown function (DUF1027) | ||
HCMCPFGN_00462 | 1.2e-146 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
HCMCPFGN_00463 | 2.2e-84 | S | Protein of unknown function (DUF1461) | |||
HCMCPFGN_00464 | 1.8e-116 | dedA | S | SNARE-like domain protein | ||
HCMCPFGN_00465 | 6.9e-150 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
HCMCPFGN_00466 | 6.5e-77 | |||||
HCMCPFGN_00469 | 2.4e-83 | S | COG NOG38524 non supervised orthologous group | |||
HCMCPFGN_00497 | 8.1e-221 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
HCMCPFGN_00498 | 4.2e-200 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
HCMCPFGN_00499 | 3.3e-178 | mprF | S | 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 | ||
HCMCPFGN_00500 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HCMCPFGN_00501 | 2.3e-29 | secG | U | Preprotein translocase | ||
HCMCPFGN_00502 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HCMCPFGN_00503 | 5.1e-78 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
HCMCPFGN_00504 | 6.5e-77 | |||||
HCMCPFGN_00505 | 3e-81 | S | COG NOG38524 non supervised orthologous group | |||
HCMCPFGN_00508 | 3.6e-168 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HCMCPFGN_00511 | 2.8e-216 | 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 | |
HCMCPFGN_00512 | 7e-262 | qacA | EGP | Major facilitator Superfamily | ||
HCMCPFGN_00513 | 5.3e-149 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
HCMCPFGN_00514 | 1.3e-119 | 3.6.1.27 | I | Acid phosphatase homologues | ||
HCMCPFGN_00515 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HCMCPFGN_00516 | 1.3e-296 | ytgP | S | Polysaccharide biosynthesis protein | ||
HCMCPFGN_00517 | 2.2e-182 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
HCMCPFGN_00518 | 3e-91 | dhaL | 2.7.1.121 | S | Dak2 | |
HCMCPFGN_00519 | 1.3e-55 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
HCMCPFGN_00520 | 7.9e-50 | |||||
HCMCPFGN_00521 | 3.4e-227 | O | Belongs to the peptidase S8 family | |||
HCMCPFGN_00522 | 6.7e-93 | O | Belongs to the peptidase S8 family | |||
HCMCPFGN_00523 | 3.2e-64 | O | Belongs to the peptidase S8 family | |||
HCMCPFGN_00524 | 5.8e-72 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
HCMCPFGN_00525 | 1.7e-15 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
HCMCPFGN_00526 | 1.7e-22 | UW | LPXTG-motif cell wall anchor domain protein | |||
HCMCPFGN_00527 | 2.1e-20 | |||||
HCMCPFGN_00528 | 5.2e-36 | CO | Thioredoxin | |||
HCMCPFGN_00529 | 7.2e-118 | M1-798 | K | Rhodanese Homology Domain | ||
HCMCPFGN_00530 | 7.7e-174 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
HCMCPFGN_00531 | 2.3e-37 | frnE | Q | DSBA-like thioredoxin domain | ||
HCMCPFGN_00532 | 8.4e-29 | frnE | Q | DSBA-like thioredoxin domain | ||
HCMCPFGN_00533 | 1.2e-25 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HCMCPFGN_00534 | 5.9e-242 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00535 | 2.6e-85 | S | Putative transposase | |||
HCMCPFGN_00536 | 6.7e-59 | S | Putative transposase | |||
HCMCPFGN_00537 | 8.5e-128 | treR | K | UTRA | ||
HCMCPFGN_00538 | 0.0 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
HCMCPFGN_00539 | 0.0 | treB | G | phosphotransferase system | ||
HCMCPFGN_00540 | 6.3e-32 | sstT | U | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
HCMCPFGN_00541 | 9e-162 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
HCMCPFGN_00542 | 5.1e-142 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
HCMCPFGN_00543 | 2.2e-243 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
HCMCPFGN_00544 | 2.6e-52 | |||||
HCMCPFGN_00545 | 7.7e-79 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_00546 | 1.5e-94 | ywnH | 2.3.1.183 | M | acetyltransferase (GNAT) family | |
HCMCPFGN_00547 | 4.1e-14 | K | Copper transport repressor CopY TcrY | |||
HCMCPFGN_00548 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
HCMCPFGN_00549 | 4.5e-152 | mdt(A) | EGP | Major facilitator Superfamily | ||
HCMCPFGN_00550 | 1e-36 | mdt(A) | EGP | Major facilitator Superfamily | ||
HCMCPFGN_00551 | 2.5e-247 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00552 | 1.3e-175 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00553 | 4.2e-139 | yxeH | S | hydrolase | ||
HCMCPFGN_00554 | 2.1e-36 | S | Enterocin A Immunity | |||
HCMCPFGN_00555 | 4.4e-225 | psd | 4.1.1.65 | I | Belongs to the phosphatidylserine decarboxylase family | |
HCMCPFGN_00556 | 4.4e-49 | pspC | KT | PspC domain | ||
HCMCPFGN_00558 | 6.4e-243 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HCMCPFGN_00559 | 6.2e-154 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
HCMCPFGN_00560 | 1.5e-110 | M | ErfK YbiS YcfS YnhG | |||
HCMCPFGN_00561 | 6.1e-91 | padR | K | Virulence activator alpha C-term | ||
HCMCPFGN_00562 | 2e-102 | padC | Q | Phenolic acid decarboxylase | ||
HCMCPFGN_00563 | 6.1e-111 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HCMCPFGN_00564 | 2.2e-12 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
HCMCPFGN_00565 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
HCMCPFGN_00566 | 3.5e-171 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
HCMCPFGN_00567 | 2.3e-90 | 3.6.1.55 | L | NUDIX domain | ||
HCMCPFGN_00568 | 2.1e-39 | |||||
HCMCPFGN_00569 | 1.7e-31 | |||||
HCMCPFGN_00570 | 3e-09 | C | WbqC-like protein family | |||
HCMCPFGN_00571 | 5.9e-180 | S | ABC transporter | |||
HCMCPFGN_00572 | 8.8e-110 | S | ABC-2 family transporter protein | |||
HCMCPFGN_00573 | 8.8e-142 | S | ABC-2 family transporter protein | |||
HCMCPFGN_00575 | 7.7e-227 | L | Transposase | |||
HCMCPFGN_00576 | 2.3e-290 | V | ABC-type multidrug transport system, ATPase and permease components | |||
HCMCPFGN_00577 | 3.2e-284 | V | ABC-type multidrug transport system, ATPase and permease components | |||
HCMCPFGN_00579 | 4.4e-16 | L | PFAM IS66 Orf2 family protein | |||
HCMCPFGN_00580 | 3.3e-09 | |||||
HCMCPFGN_00581 | 9.6e-14 | S | Phage derived protein Gp49-like (DUF891) | |||
HCMCPFGN_00582 | 1.5e-40 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_00583 | 7.6e-42 | |||||
HCMCPFGN_00584 | 2.2e-53 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
HCMCPFGN_00585 | 1.5e-242 | L | Probable transposase | |||
HCMCPFGN_00586 | 2.5e-14 | S | Fic/DOC family | |||
HCMCPFGN_00587 | 4e-19 | L | IS1381, transposase OrfA | |||
HCMCPFGN_00588 | 8.6e-34 | L | IS1381, transposase OrfA | |||
HCMCPFGN_00589 | 3.3e-83 | racA | K | Domain of unknown function (DUF1836) | ||
HCMCPFGN_00590 | 4e-153 | yitS | S | EDD domain protein, DegV family | ||
HCMCPFGN_00592 | 4.2e-20 | UW | LPXTG-motif cell wall anchor domain protein | |||
HCMCPFGN_00593 | 8.4e-148 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
HCMCPFGN_00594 | 4.9e-54 | |||||
HCMCPFGN_00595 | 2.9e-139 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
HCMCPFGN_00596 | 2.2e-134 | mgtC | S | MgtC family | ||
HCMCPFGN_00597 | 1.9e-09 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
HCMCPFGN_00598 | 2.8e-162 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HCMCPFGN_00599 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HCMCPFGN_00600 | 3.6e-55 | yheA | S | Belongs to the UPF0342 family | ||
HCMCPFGN_00601 | 7.7e-230 | yhaO | L | Ser Thr phosphatase family protein | ||
HCMCPFGN_00602 | 0.0 | L | AAA domain | |||
HCMCPFGN_00603 | 4.5e-188 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HCMCPFGN_00604 | 1.3e-48 | S | PAS domain | |||
HCMCPFGN_00605 | 1.6e-213 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_00606 | 1.3e-154 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HCMCPFGN_00607 | 8e-28 | |||||
HCMCPFGN_00608 | 3.4e-79 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
HCMCPFGN_00609 | 3.8e-54 | higA | K | Helix-turn-helix XRE-family like proteins | ||
HCMCPFGN_00610 | 3.9e-136 | ecsA | V | ABC transporter, ATP-binding protein | ||
HCMCPFGN_00611 | 1.7e-213 | ecsB | U | ABC transporter | ||
HCMCPFGN_00612 | 1e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HCMCPFGN_00613 | 7.3e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
HCMCPFGN_00614 | 3.3e-123 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HCMCPFGN_00615 | 2.3e-66 | S | SLAP domain | |||
HCMCPFGN_00616 | 1.1e-223 | S | SLAP domain | |||
HCMCPFGN_00617 | 9.7e-255 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HCMCPFGN_00618 | 8.7e-176 | S | SLAP domain | |||
HCMCPFGN_00619 | 2.3e-69 | M | Peptidase family M1 domain | |||
HCMCPFGN_00620 | 5.9e-140 | M | Peptidase family M1 domain | |||
HCMCPFGN_00621 | 1.3e-38 | M | Peptidase family M1 domain | |||
HCMCPFGN_00622 | 2.9e-195 | S | Bacteriocin helveticin-J | |||
HCMCPFGN_00623 | 3.8e-20 | |||||
HCMCPFGN_00624 | 4.3e-52 | L | RelB antitoxin | |||
HCMCPFGN_00625 | 4.8e-141 | qmcA | O | prohibitin homologues | ||
HCMCPFGN_00626 | 7.5e-123 | darA | C | Flavodoxin | ||
HCMCPFGN_00627 | 1.3e-309 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HCMCPFGN_00628 | 1.9e-78 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HCMCPFGN_00629 | 3.2e-217 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
HCMCPFGN_00630 | 3.9e-133 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HCMCPFGN_00631 | 1.9e-37 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HCMCPFGN_00632 | 2.3e-119 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HCMCPFGN_00633 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
HCMCPFGN_00634 | 1.5e-275 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HCMCPFGN_00635 | 1.2e-194 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HCMCPFGN_00636 | 3.2e-104 | 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 | |
HCMCPFGN_00637 | 3.2e-289 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HCMCPFGN_00638 | 4.6e-238 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HCMCPFGN_00639 | 0.0 | cas3 | L | Type III restriction enzyme, res subunit | ||
HCMCPFGN_00640 | 1.1e-143 | cas5d | S | CRISPR-associated protein (Cas_Cas5) | ||
HCMCPFGN_00641 | 0.0 | csd1 | 3.5.1.28 | M | CRISPR-associated protein (Cas_Csd1) | |
HCMCPFGN_00642 | 9.3e-158 | csd2 | L | CRISPR-associated protein Cas7 | ||
HCMCPFGN_00643 | 2.8e-125 | cas4 | 3.1.12.1 | L | Domain of unknown function DUF83 | |
HCMCPFGN_00644 | 2.9e-198 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HCMCPFGN_00645 | 1.4e-28 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
HCMCPFGN_00646 | 9e-14 | |||||
HCMCPFGN_00647 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HCMCPFGN_00648 | 4.5e-157 | 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 | |
HCMCPFGN_00649 | 1.4e-104 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HCMCPFGN_00650 | 4.1e-83 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HCMCPFGN_00651 | 2.6e-247 | dnaB | L | Replication initiation and membrane attachment | ||
HCMCPFGN_00652 | 1.7e-165 | dnaI | L | Primosomal protein DnaI | ||
HCMCPFGN_00653 | 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) | |
HCMCPFGN_00654 | 1.5e-89 | |||||
HCMCPFGN_00655 | 4.1e-95 | |||||
HCMCPFGN_00656 | 2.9e-184 | S | Domain of unknown function (DUF389) | |||
HCMCPFGN_00657 | 9.3e-30 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
HCMCPFGN_00658 | 5.2e-139 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
HCMCPFGN_00659 | 8.9e-37 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
HCMCPFGN_00660 | 1.8e-54 | 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 | ||
HCMCPFGN_00661 | 1.8e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HCMCPFGN_00662 | 5.1e-57 | 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 | ||
HCMCPFGN_00663 | 3.8e-93 | yqeG | S | HAD phosphatase, family IIIA | ||
HCMCPFGN_00664 | 4.3e-211 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
HCMCPFGN_00665 | 2.4e-121 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HCMCPFGN_00666 | 2.3e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
HCMCPFGN_00667 | 6.9e-59 | 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 | ||
HCMCPFGN_00668 | 6.6e-215 | ylbM | S | Belongs to the UPF0348 family | ||
HCMCPFGN_00669 | 1e-96 | yceD | S | Uncharacterized ACR, COG1399 | ||
HCMCPFGN_00670 | 3.2e-127 | K | response regulator | |||
HCMCPFGN_00671 | 4.6e-280 | arlS | 2.7.13.3 | T | Histidine kinase | |
HCMCPFGN_00672 | 1.5e-236 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00673 | 6.4e-27 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_00674 | 1.4e-203 | S | Bacteriocin helveticin-J | |||
HCMCPFGN_00675 | 8e-244 | slpX | S | SLAP domain | ||
HCMCPFGN_00676 | 2.7e-56 | L | Integrase | |||
HCMCPFGN_00677 | 7.9e-171 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00678 | 1.4e-49 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00679 | 1e-84 | S | Aminoacyl-tRNA editing domain | |||
HCMCPFGN_00680 | 4.9e-155 | 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 | ||
HCMCPFGN_00681 | 4.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HCMCPFGN_00682 | 3.1e-136 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HCMCPFGN_00683 | 1.5e-61 | yodB | K | Transcriptional regulator, HxlR family | ||
HCMCPFGN_00684 | 2e-202 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
HCMCPFGN_00685 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HCMCPFGN_00686 | 9.2e-62 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
HCMCPFGN_00687 | 1.6e-168 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
HCMCPFGN_00688 | 2.8e-26 | S | Phage derived protein Gp49-like (DUF891) | |||
HCMCPFGN_00689 | 9e-38 | K | Helix-turn-helix domain | |||
HCMCPFGN_00690 | 1.5e-169 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
HCMCPFGN_00691 | 0.0 | S | membrane | |||
HCMCPFGN_00692 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
HCMCPFGN_00693 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HCMCPFGN_00694 | 1.7e-99 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
HCMCPFGN_00695 | 3.2e-116 | gluP | 3.4.21.105 | S | Rhomboid family | |
HCMCPFGN_00696 | 5.6e-33 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
HCMCPFGN_00697 | 4.5e-70 | yqhL | P | Rhodanese-like protein | ||
HCMCPFGN_00698 | 3.6e-171 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
HCMCPFGN_00699 | 2.6e-30 | ynbB | 4.4.1.1 | P | aluminum resistance | |
HCMCPFGN_00700 | 5.1e-170 | ynbB | 4.4.1.1 | P | aluminum resistance | |
HCMCPFGN_00701 | 1.5e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HCMCPFGN_00702 | 1.8e-135 | |||||
HCMCPFGN_00703 | 7.1e-164 | |||||
HCMCPFGN_00704 | 2.7e-148 | |||||
HCMCPFGN_00705 | 1e-238 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_00706 | 1.2e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
HCMCPFGN_00707 | 1.7e-187 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
HCMCPFGN_00708 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
HCMCPFGN_00709 | 1.2e-188 | lacR | K | Transcriptional regulator | ||
HCMCPFGN_00710 | 2e-244 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00711 | 2.1e-24 | lacS | G | Transporter | ||
HCMCPFGN_00712 | 1.4e-48 | lacS | G | Transporter | ||
HCMCPFGN_00713 | 1.1e-108 | lacS | G | Transporter | ||
HCMCPFGN_00714 | 0.0 | lacS | G | Transporter | ||
HCMCPFGN_00715 | 3.8e-89 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
HCMCPFGN_00716 | 2e-44 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
HCMCPFGN_00717 | 5.2e-78 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00718 | 1.5e-166 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00719 | 1.5e-112 | |||||
HCMCPFGN_00720 | 1.7e-165 | hprA | 1.1.1.29 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_00721 | 3.5e-46 | |||||
HCMCPFGN_00722 | 1.4e-53 | |||||
HCMCPFGN_00723 | 5.1e-68 | ptsG | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
HCMCPFGN_00724 | 4e-218 | naiP | EGP | Major facilitator Superfamily | ||
HCMCPFGN_00725 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
HCMCPFGN_00726 | 4.6e-263 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00727 | 6.1e-291 | oppA | E | ABC transporter | ||
HCMCPFGN_00728 | 1.7e-213 | Q | Imidazolonepropionase and related amidohydrolases | |||
HCMCPFGN_00729 | 3e-61 | psiE | S | Phosphate-starvation-inducible E | ||
HCMCPFGN_00731 | 3e-223 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
HCMCPFGN_00732 | 1.3e-287 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
HCMCPFGN_00733 | 2.9e-195 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
HCMCPFGN_00734 | 2.2e-96 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_00735 | 7.8e-33 | K | response regulator | |||
HCMCPFGN_00736 | 5.6e-37 | K | response regulator | |||
HCMCPFGN_00737 | 1.3e-50 | sptS | 2.7.13.3 | T | Histidine kinase | |
HCMCPFGN_00738 | 6.1e-116 | sptS | 2.7.13.3 | T | Histidine kinase | |
HCMCPFGN_00739 | 4.7e-208 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_00740 | 9.2e-71 | O | OsmC-like protein | |||
HCMCPFGN_00741 | 1.1e-124 | dkgA | 1.1.1.346 | S | L-ascorbic acid biosynthetic process | |
HCMCPFGN_00742 | 1e-91 | |||||
HCMCPFGN_00743 | 4.2e-247 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_00745 | 6.1e-74 | |||||
HCMCPFGN_00746 | 8.3e-60 | |||||
HCMCPFGN_00747 | 3.9e-39 | |||||
HCMCPFGN_00748 | 1.5e-272 | yjeM | E | Amino Acid | ||
HCMCPFGN_00749 | 1.8e-89 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
HCMCPFGN_00750 | 9.4e-195 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
HCMCPFGN_00753 | 2.9e-90 | |||||
HCMCPFGN_00754 | 1.2e-227 | L | Transposase | |||
HCMCPFGN_00755 | 1.7e-14 | |||||
HCMCPFGN_00756 | 4.3e-16 | |||||
HCMCPFGN_00757 | 1.4e-57 | |||||
HCMCPFGN_00758 | 2.5e-07 | |||||
HCMCPFGN_00760 | 3.4e-37 | |||||
HCMCPFGN_00761 | 1.1e-52 | S | SLAP domain | |||
HCMCPFGN_00762 | 4.4e-222 | L | Transposase | |||
HCMCPFGN_00763 | 2.1e-26 | S | response to antibiotic | |||
HCMCPFGN_00764 | 3.4e-194 | S | response to antibiotic | |||
HCMCPFGN_00765 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
HCMCPFGN_00766 | 1.4e-275 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
HCMCPFGN_00767 | 4.1e-39 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
HCMCPFGN_00768 | 8e-157 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_00769 | 4e-52 | hsdS | 3.1.21.3 | L | PFAM restriction modification system DNA specificity domain | |
HCMCPFGN_00771 | 9.9e-233 | S | Domain of unknown function (DUF3883) | |||
HCMCPFGN_00772 | 1.6e-216 | S | SLAP domain | |||
HCMCPFGN_00774 | 1.1e-30 | |||||
HCMCPFGN_00776 | 3.2e-115 | G | Peptidase_C39 like family | |||
HCMCPFGN_00777 | 3.3e-12 | G | Peptidase_C39 like family | |||
HCMCPFGN_00778 | 1.1e-87 | M | NlpC/P60 family | |||
HCMCPFGN_00779 | 4.6e-64 | M | NlpC/P60 family | |||
HCMCPFGN_00780 | 1.8e-53 | S | Iron-sulfur cluster assembly protein | |||
HCMCPFGN_00781 | 6.5e-146 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
HCMCPFGN_00782 | 7.6e-123 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
HCMCPFGN_00783 | 3.3e-38 | |||||
HCMCPFGN_00784 | 3e-45 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_00785 | 9e-54 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_00786 | 1.7e-114 | papP | P | ABC transporter, permease protein | ||
HCMCPFGN_00787 | 4.8e-117 | P | ABC transporter permease | |||
HCMCPFGN_00788 | 8.2e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HCMCPFGN_00789 | 1.7e-162 | cjaA | ET | ABC transporter substrate-binding protein | ||
HCMCPFGN_00790 | 2.5e-52 | S | Iron-sulfur cluster assembly protein | |||
HCMCPFGN_00791 | 9.5e-43 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
HCMCPFGN_00792 | 9.4e-91 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
HCMCPFGN_00793 | 1.3e-30 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
HCMCPFGN_00794 | 3.3e-14 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
HCMCPFGN_00795 | 9.7e-46 | |||||
HCMCPFGN_00796 | 4.2e-97 | S | Cysteine-rich secretory protein family | |||
HCMCPFGN_00797 | 4.3e-49 | |||||
HCMCPFGN_00798 | 4.6e-206 | G | Major Facilitator Superfamily | |||
HCMCPFGN_00799 | 1.5e-51 | |||||
HCMCPFGN_00800 | 2.8e-243 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_00801 | 1.8e-46 | S | Domain of unknown function (DUF4160) | |||
HCMCPFGN_00802 | 3.3e-39 | XK27_08875 | O | Matrixin | ||
HCMCPFGN_00803 | 2.6e-212 | clcA | P | chloride | ||
HCMCPFGN_00804 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
HCMCPFGN_00805 | 1.6e-161 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
HCMCPFGN_00806 | 1.7e-167 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
HCMCPFGN_00807 | 7.9e-248 | xylG | 3.6.3.17 | S | ABC transporter | |
HCMCPFGN_00808 | 9.4e-179 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
HCMCPFGN_00809 | 2.2e-17 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
HCMCPFGN_00810 | 2.3e-218 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00811 | 1.6e-35 | 2.4.2.6 | F | nucleoside 2-deoxyribosyltransferase | ||
HCMCPFGN_00812 | 1.4e-11 | 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 | |
HCMCPFGN_00813 | 1.6e-28 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_00814 | 1.2e-152 | ydiM | G | Major facilitator superfamily | ||
HCMCPFGN_00816 | 6.1e-72 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
HCMCPFGN_00817 | 5.5e-63 | L | Transposase | |||
HCMCPFGN_00818 | 8.7e-113 | 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) | |
HCMCPFGN_00819 | 2.9e-120 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
HCMCPFGN_00820 | 1.1e-164 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
HCMCPFGN_00821 | 1.1e-92 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HCMCPFGN_00822 | 1.8e-181 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HCMCPFGN_00823 | 1.4e-242 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HCMCPFGN_00824 | 4.2e-211 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HCMCPFGN_00825 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HCMCPFGN_00826 | 4.3e-08 | yfdK | S | phosphatase homologous to the C-terminal domain of histone macroH2A1 | ||
HCMCPFGN_00827 | 7.4e-222 | E | IrrE N-terminal-like domain | |||
HCMCPFGN_00828 | 1.5e-108 | S | Domain of unknown function (DUF4411) | |||
HCMCPFGN_00829 | 1.9e-84 | glcU | U | sugar transport | ||
HCMCPFGN_00830 | 2.3e-43 | glcU | U | sugar transport | ||
HCMCPFGN_00831 | 2.9e-47 | |||||
HCMCPFGN_00832 | 2.3e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
HCMCPFGN_00833 | 8.5e-18 | |||||
HCMCPFGN_00834 | 1.5e-16 | |||||
HCMCPFGN_00835 | 4.2e-80 | K | Acetyltransferase (GNAT) domain | |||
HCMCPFGN_00836 | 4.9e-148 | S | Protein of unknown function (DUF2785) | |||
HCMCPFGN_00837 | 4.7e-26 | S | MazG-like family | |||
HCMCPFGN_00838 | 4.4e-56 | |||||
HCMCPFGN_00839 | 3.3e-43 | |||||
HCMCPFGN_00840 | 2.9e-31 | S | Protein of unknown function (DUF3923) | |||
HCMCPFGN_00841 | 8e-51 | 3.6.1.55 | F | NUDIX domain | ||
HCMCPFGN_00842 | 6.8e-162 | yxaM | EGP | Major facilitator Superfamily | ||
HCMCPFGN_00843 | 1.1e-21 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
HCMCPFGN_00844 | 4.2e-32 | cdd | 2.4.2.4, 3.5.4.5 | F | cytidine deaminase activity | |
HCMCPFGN_00845 | 9e-92 | S | AAA domain | |||
HCMCPFGN_00846 | 2e-149 | 2.7.1.89 | M | Phosphotransferase enzyme family | ||
HCMCPFGN_00847 | 1.8e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HCMCPFGN_00848 | 1.3e-103 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HCMCPFGN_00849 | 3.7e-24 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HCMCPFGN_00850 | 2.5e-120 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
HCMCPFGN_00851 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
HCMCPFGN_00852 | 6.9e-62 | S | Bacterial PH domain | |||
HCMCPFGN_00853 | 4e-27 | |||||
HCMCPFGN_00854 | 1.1e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
HCMCPFGN_00855 | 2.5e-177 | I | Carboxylesterase family | |||
HCMCPFGN_00856 | 2.3e-262 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_00858 | 4.8e-200 | M | Glycosyl hydrolases family 25 | |||
HCMCPFGN_00859 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
HCMCPFGN_00860 | 8e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
HCMCPFGN_00861 | 9.5e-129 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
HCMCPFGN_00862 | 1.5e-199 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
HCMCPFGN_00863 | 2e-255 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
HCMCPFGN_00864 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HCMCPFGN_00865 | 1e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HCMCPFGN_00866 | 7.5e-200 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
HCMCPFGN_00867 | 9.2e-101 | 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 | ||
HCMCPFGN_00868 | 5.3e-69 | yqhY | S | Asp23 family, cell envelope-related function | ||
HCMCPFGN_00869 | 4e-63 | 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 | ||
HCMCPFGN_00870 | 4e-153 | 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 | |
HCMCPFGN_00871 | 1.5e-194 | 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 | |
HCMCPFGN_00872 | 2.9e-35 | 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 | |
HCMCPFGN_00873 | 2.1e-157 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
HCMCPFGN_00874 | 6.2e-151 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HCMCPFGN_00875 | 9.1e-306 | recN | L | May be involved in recombinational repair of damaged DNA | ||
HCMCPFGN_00876 | 8.4e-78 | 6.3.3.2 | S | ASCH | ||
HCMCPFGN_00877 | 1.2e-109 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
HCMCPFGN_00878 | 9.4e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
HCMCPFGN_00879 | 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 | ||
HCMCPFGN_00880 | 2.5e-172 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
HCMCPFGN_00881 | 4.1e-245 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HCMCPFGN_00882 | 9.2e-147 | stp | 3.1.3.16 | T | phosphatase | |
HCMCPFGN_00883 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
HCMCPFGN_00884 | 1.7e-165 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
HCMCPFGN_00885 | 9.4e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
HCMCPFGN_00886 | 8.4e-125 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HCMCPFGN_00887 | 5.7e-49 | |||||
HCMCPFGN_00888 | 2.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
HCMCPFGN_00889 | 6.8e-57 | asp | S | Asp23 family, cell envelope-related function | ||
HCMCPFGN_00890 | 2.2e-304 | yloV | S | DAK2 domain fusion protein YloV | ||
HCMCPFGN_00891 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
HCMCPFGN_00892 | 2.9e-182 | 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 | |
HCMCPFGN_00893 | 9.8e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HCMCPFGN_00894 | 1.7e-193 | oppD | P | Belongs to the ABC transporter superfamily | ||
HCMCPFGN_00895 | 1.2e-180 | oppF | P | Belongs to the ABC transporter superfamily | ||
HCMCPFGN_00896 | 6.6e-176 | oppB | P | ABC transporter permease | ||
HCMCPFGN_00897 | 1.9e-143 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
HCMCPFGN_00898 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
HCMCPFGN_00899 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
HCMCPFGN_00900 | 1.3e-125 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
HCMCPFGN_00901 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
HCMCPFGN_00902 | 4.9e-166 | 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) | ||
HCMCPFGN_00903 | 1.7e-289 | pipD | E | Dipeptidase | ||
HCMCPFGN_00904 | 1.8e-44 | |||||
HCMCPFGN_00905 | 2.4e-259 | yfnA | E | amino acid | ||
HCMCPFGN_00906 | 1.7e-193 | L | Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_00907 | 3.2e-56 | 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 | ||
HCMCPFGN_00908 | 1.9e-227 | 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 | |
HCMCPFGN_00909 | 4.5e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
HCMCPFGN_00910 | 4.1e-92 | 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 | ||
HCMCPFGN_00911 | 1.7e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HCMCPFGN_00912 | 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 | ||
HCMCPFGN_00913 | 9.2e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
HCMCPFGN_00914 | 2.1e-148 | E | GDSL-like Lipase/Acylhydrolase family | |||
HCMCPFGN_00915 | 1.5e-112 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
HCMCPFGN_00916 | 4.3e-37 | ynzC | S | UPF0291 protein | ||
HCMCPFGN_00917 | 4.2e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
HCMCPFGN_00918 | 1e-296 | mdlA | V | ABC transporter | ||
HCMCPFGN_00919 | 1.2e-300 | mdlB | V | ABC transporter | ||
HCMCPFGN_00920 | 2.5e-31 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HCMCPFGN_00921 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HCMCPFGN_00922 | 3.2e-225 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
HCMCPFGN_00923 | 8.6e-113 | plsC | 2.3.1.51 | I | Acyltransferase | |
HCMCPFGN_00924 | 1.7e-198 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
HCMCPFGN_00925 | 1.2e-140 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HCMCPFGN_00926 | 3.1e-184 | 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 | ||
HCMCPFGN_00927 | 7e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HCMCPFGN_00928 | 3.4e-92 | 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 | ||
HCMCPFGN_00929 | 7.8e-137 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HCMCPFGN_00930 | 1.6e-146 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
HCMCPFGN_00931 | 1.5e-196 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HCMCPFGN_00932 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
HCMCPFGN_00933 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HCMCPFGN_00934 | 5.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
HCMCPFGN_00935 | 1.7e-194 | nusA | K | Participates in both transcription termination and antitermination | ||
HCMCPFGN_00936 | 3e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
HCMCPFGN_00937 | 1e-45 | rplGA | J | ribosomal protein | ||
HCMCPFGN_00938 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
HCMCPFGN_00939 | 3.3e-59 | 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 | ||
HCMCPFGN_00940 | 9.8e-166 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
HCMCPFGN_00941 | 2.3e-181 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
HCMCPFGN_00942 | 4.5e-186 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HCMCPFGN_00943 | 8.2e-81 | 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 | ||
HCMCPFGN_00944 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
HCMCPFGN_00945 | 3.9e-199 | 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 | ||
HCMCPFGN_00946 | 9.8e-172 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_00947 | 2.2e-96 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_00948 | 3.8e-15 | |||||
HCMCPFGN_00949 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
HCMCPFGN_00950 | 4.5e-118 | srtA | 3.4.22.70 | M | sortase family | |
HCMCPFGN_00951 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
HCMCPFGN_00952 | 1.8e-95 | 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 | |
HCMCPFGN_00953 | 4.4e-169 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
HCMCPFGN_00954 | 7.9e-151 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
HCMCPFGN_00955 | 2.7e-253 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
HCMCPFGN_00956 | 2.4e-84 | 3.4.21.96 | S | SLAP domain | ||
HCMCPFGN_00957 | 0.0 | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
HCMCPFGN_00958 | 5.1e-156 | lysR5 | K | LysR substrate binding domain | ||
HCMCPFGN_00959 | 7.1e-22 | arcA | 3.5.3.6 | E | Arginine | |
HCMCPFGN_00960 | 6.6e-15 | arcA | 3.5.3.6 | E | Arginine | |
HCMCPFGN_00961 | 7.1e-90 | arcA | 3.5.3.6 | E | Arginine | |
HCMCPFGN_00962 | 1.1e-12 | argF | 2.1.3.3, 2.7.2.2 | 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 | |
HCMCPFGN_00963 | 1.5e-144 | argF | 2.1.3.3, 2.7.2.2 | 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 | |
HCMCPFGN_00964 | 9.9e-68 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
HCMCPFGN_00965 | 2.8e-52 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
HCMCPFGN_00966 | 8.4e-96 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
HCMCPFGN_00967 | 3.1e-212 | S | Sterol carrier protein domain | |||
HCMCPFGN_00968 | 2.5e-19 | |||||
HCMCPFGN_00969 | 5.9e-106 | K | LysR substrate binding domain | |||
HCMCPFGN_00970 | 2.4e-74 | |||||
HCMCPFGN_00971 | 7.9e-28 | S | amino acid activation for nonribosomal peptide biosynthetic process | |||
HCMCPFGN_00972 | 7e-115 | 3.6.3.44 | V | ABC transporter transmembrane region | ||
HCMCPFGN_00974 | 1.5e-186 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HCMCPFGN_00975 | 7.1e-246 | thrC | 4.2.3.1 | E | Threonine synthase | |
HCMCPFGN_00976 | 1.6e-122 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HCMCPFGN_00977 | 8.6e-110 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
HCMCPFGN_00978 | 1.5e-107 | |||||
HCMCPFGN_00979 | 1.4e-161 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
HCMCPFGN_00980 | 1.3e-39 | S | Peptidase family M23 | |||
HCMCPFGN_00981 | 6.8e-153 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
HCMCPFGN_00982 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HCMCPFGN_00983 | 3.2e-69 | yqeY | S | YqeY-like protein | ||
HCMCPFGN_00984 | 8.9e-173 | phoH | T | phosphate starvation-inducible protein PhoH | ||
HCMCPFGN_00985 | 3.2e-92 | 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 | |
HCMCPFGN_00986 | 1.8e-167 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HCMCPFGN_00987 | 1e-136 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HCMCPFGN_00988 | 4.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HCMCPFGN_00989 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
HCMCPFGN_00990 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
HCMCPFGN_00991 | 4.6e-197 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
HCMCPFGN_00992 | 6.8e-124 | S | Peptidase family M23 | |||
HCMCPFGN_00993 | 3.6e-68 | mutT | 3.6.1.55 | F | NUDIX domain | |
HCMCPFGN_00994 | 2.4e-124 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
HCMCPFGN_00995 | 1e-153 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
HCMCPFGN_00996 | 1.4e-242 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
HCMCPFGN_00997 | 3.9e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
HCMCPFGN_00998 | 2.8e-123 | skfE | V | ATPases associated with a variety of cellular activities | ||
HCMCPFGN_00999 | 1.6e-146 | |||||
HCMCPFGN_01000 | 2.5e-147 | |||||
HCMCPFGN_01001 | 1.6e-129 | |||||
HCMCPFGN_01002 | 4.9e-10 | rarA | L | recombination factor protein RarA | ||
HCMCPFGN_01003 | 9.8e-115 | rarA | L | recombination factor protein RarA | ||
HCMCPFGN_01004 | 7.8e-28 | |||||
HCMCPFGN_01005 | 3e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HCMCPFGN_01006 | 2.7e-140 | |||||
HCMCPFGN_01007 | 1.8e-176 | |||||
HCMCPFGN_01008 | 2.8e-260 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
HCMCPFGN_01009 | 1.6e-185 | 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) | |
HCMCPFGN_01010 | 4.2e-203 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
HCMCPFGN_01011 | 2.2e-179 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
HCMCPFGN_01012 | 1.1e-167 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
HCMCPFGN_01013 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
HCMCPFGN_01014 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
HCMCPFGN_01015 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
HCMCPFGN_01016 | 1.1e-89 | ypmB | S | Protein conserved in bacteria | ||
HCMCPFGN_01017 | 1.2e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
HCMCPFGN_01018 | 7.4e-115 | dnaD | L | DnaD domain protein | ||
HCMCPFGN_01019 | 5.1e-113 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
HCMCPFGN_01020 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
HCMCPFGN_01021 | 3.5e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
HCMCPFGN_01022 | 8.6e-107 | ypsA | S | Belongs to the UPF0398 family | ||
HCMCPFGN_01023 | 8e-70 | 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 | ||
HCMCPFGN_01024 | 2.9e-215 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HCMCPFGN_01025 | 2.4e-201 | cpdA | S | Calcineurin-like phosphoesterase | ||
HCMCPFGN_01026 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
HCMCPFGN_01027 | 9.5e-80 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HCMCPFGN_01028 | 5e-157 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HCMCPFGN_01029 | 2.3e-198 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
HCMCPFGN_01030 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
HCMCPFGN_01031 | 5.7e-149 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01032 | 5.9e-79 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01033 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
HCMCPFGN_01034 | 7.7e-65 | |||||
HCMCPFGN_01035 | 1.8e-159 | degV | S | EDD domain protein, DegV family | ||
HCMCPFGN_01036 | 7.6e-205 | xerS | L | Belongs to the 'phage' integrase family | ||
HCMCPFGN_01037 | 2.7e-63 | |||||
HCMCPFGN_01038 | 5.9e-88 | adk | 2.7.4.3 | F | topology modulation protein | |
HCMCPFGN_01039 | 4.4e-109 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
HCMCPFGN_01040 | 1.3e-52 | |||||
HCMCPFGN_01041 | 1.2e-26 | M | Glycosyl hydrolases family 25 | |||
HCMCPFGN_01042 | 3.4e-92 | M | Glycosyl hydrolases family 25 | |||
HCMCPFGN_01043 | 3.3e-24 | lysA2 | M | Glycosyl hydrolases family 25 | ||
HCMCPFGN_01044 | 3.5e-36 | S | Transglycosylase associated protein | |||
HCMCPFGN_01045 | 3.4e-166 | L | Transposase | |||
HCMCPFGN_01046 | 2.8e-27 | L | Transposase | |||
HCMCPFGN_01047 | 5.9e-87 | yoaK | S | Protein of unknown function (DUF1275) | ||
HCMCPFGN_01048 | 6.2e-55 | K | Helix-turn-helix domain | |||
HCMCPFGN_01049 | 5.9e-111 | 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 | |
HCMCPFGN_01050 | 3.3e-164 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
HCMCPFGN_01051 | 3.8e-171 | K | Transcriptional regulator | |||
HCMCPFGN_01052 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
HCMCPFGN_01053 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
HCMCPFGN_01054 | 1.5e-107 | 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 | |
HCMCPFGN_01055 | 1.4e-102 | snf | 2.7.11.1 | KL | domain protein | |
HCMCPFGN_01056 | 2.9e-71 | snf | 2.7.11.1 | KL | domain protein | |
HCMCPFGN_01057 | 4.9e-203 | snf | 2.7.11.1 | KL | domain protein | |
HCMCPFGN_01058 | 3.9e-43 | snf | 2.7.11.1 | KL | domain protein | |
HCMCPFGN_01059 | 7.1e-18 | snf | 2.7.11.1 | KL | domain protein | |
HCMCPFGN_01060 | 7.8e-32 | |||||
HCMCPFGN_01061 | 9.1e-18 | |||||
HCMCPFGN_01062 | 5.8e-85 | dps | P | Belongs to the Dps family | ||
HCMCPFGN_01063 | 4.4e-94 | K | acetyltransferase | |||
HCMCPFGN_01064 | 5.3e-79 | K | COG COG0846 NAD-dependent protein deacetylases, SIR2 family | |||
HCMCPFGN_01065 | 1.1e-71 | K | COG COG0846 NAD-dependent protein deacetylases, SIR2 family | |||
HCMCPFGN_01066 | 1.8e-49 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HCMCPFGN_01067 | 1.5e-39 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HCMCPFGN_01068 | 1.6e-108 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HCMCPFGN_01069 | 1.9e-83 | K | Bacterial regulatory proteins, tetR family | |||
HCMCPFGN_01070 | 1.8e-93 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01071 | 6.4e-184 | XK27_08635 | S | UPF0210 protein | ||
HCMCPFGN_01072 | 6.4e-30 | 1.1.1.3 | T | phosphoserine phosphatase activity | ||
HCMCPFGN_01073 | 9.9e-143 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
HCMCPFGN_01074 | 3e-60 | S | Hydrolases of the alpha beta superfamily | |||
HCMCPFGN_01075 | 7.1e-29 | S | Hydrolases of the alpha beta superfamily | |||
HCMCPFGN_01076 | 5.3e-52 | S | Alpha beta hydrolase | |||
HCMCPFGN_01077 | 1.7e-22 | K | Acetyltransferase (GNAT) family | |||
HCMCPFGN_01078 | 6.4e-48 | K | Acetyltransferase (GNAT) family | |||
HCMCPFGN_01079 | 2e-255 | gor | 1.8.1.7 | C | Glutathione reductase | |
HCMCPFGN_01080 | 9.9e-117 | L | Integrase | |||
HCMCPFGN_01082 | 1.5e-197 | L | hmm pf00665 | |||
HCMCPFGN_01083 | 8.3e-42 | L | Helix-turn-helix domain | |||
HCMCPFGN_01084 | 2.3e-72 | L | Helix-turn-helix domain | |||
HCMCPFGN_01085 | 9.1e-161 | cjaA | ET | ABC transporter substrate-binding protein | ||
HCMCPFGN_01086 | 5.3e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HCMCPFGN_01087 | 3.1e-87 | P | ABC transporter permease | |||
HCMCPFGN_01088 | 6e-112 | papP | P | ABC transporter, permease protein | ||
HCMCPFGN_01089 | 1e-69 | adhR | K | helix_turn_helix, mercury resistance | ||
HCMCPFGN_01090 | 8.2e-27 | S | Uncharacterized protein conserved in bacteria (DUF2255) | |||
HCMCPFGN_01091 | 2.6e-109 | G | Antibiotic biosynthesis monooxygenase | |||
HCMCPFGN_01092 | 3e-94 | lacA | 2.3.1.79 | S | Maltose acetyltransferase | |
HCMCPFGN_01093 | 1e-125 | 4.1.1.45 | S | Amidohydrolase | ||
HCMCPFGN_01095 | 8.5e-66 | S | Abi-like protein | |||
HCMCPFGN_01096 | 1.5e-84 | kptA | H | Removes the 2'-phosphate from RNA via an intermediate in which the phosphate is ADP-ribosylated by NAD followed by a presumed transesterification to release the RNA and generate ADP- ribose 1''-2''-cyclic phosphate (APPR P). May function as an ADP- ribosylase | ||
HCMCPFGN_01097 | 9.1e-71 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
HCMCPFGN_01098 | 2.1e-32 | |||||
HCMCPFGN_01099 | 8.8e-229 | yrvN | L | AAA C-terminal domain | ||
HCMCPFGN_01100 | 8.9e-140 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
HCMCPFGN_01101 | 2.4e-51 | |||||
HCMCPFGN_01102 | 2e-22 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_01103 | 8e-125 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
HCMCPFGN_01104 | 1e-41 | |||||
HCMCPFGN_01105 | 1.6e-76 | K | LytTr DNA-binding domain | |||
HCMCPFGN_01106 | 3e-53 | S | Protein of unknown function (DUF3021) | |||
HCMCPFGN_01107 | 4.6e-88 | XK27_09675 | K | Acetyltransferase (GNAT) domain | ||
HCMCPFGN_01108 | 7.4e-138 | |||||
HCMCPFGN_01109 | 9.6e-47 | |||||
HCMCPFGN_01110 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
HCMCPFGN_01111 | 1.2e-188 | V | Beta-lactamase | |||
HCMCPFGN_01112 | 1.1e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
HCMCPFGN_01113 | 9.3e-232 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01114 | 1.4e-43 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
HCMCPFGN_01115 | 3e-68 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
HCMCPFGN_01116 | 3.8e-68 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
HCMCPFGN_01118 | 2.2e-85 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HCMCPFGN_01119 | 3.7e-82 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
HCMCPFGN_01120 | 6.5e-22 | |||||
HCMCPFGN_01121 | 5.3e-28 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
HCMCPFGN_01122 | 1.9e-243 | ubiX | 2.5.1.129, 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
HCMCPFGN_01123 | 4.5e-45 | K | LysR substrate binding domain | |||
HCMCPFGN_01124 | 1.2e-13 | S | Protein of unknown function (DUF554) | |||
HCMCPFGN_01125 | 2e-68 | S | Protein of unknown function (DUF554) | |||
HCMCPFGN_01126 | 6.4e-241 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
HCMCPFGN_01127 | 2.6e-55 | |||||
HCMCPFGN_01128 | 1.2e-37 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
HCMCPFGN_01129 | 2.1e-121 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
HCMCPFGN_01130 | 3e-37 | |||||
HCMCPFGN_01131 | 4.7e-102 | S | LexA-binding, inner membrane-associated putative hydrolase | |||
HCMCPFGN_01132 | 7.4e-92 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HCMCPFGN_01133 | 7.1e-257 | S | C4-dicarboxylate anaerobic carrier | |||
HCMCPFGN_01134 | 2.2e-207 | |||||
HCMCPFGN_01135 | 6.1e-87 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
HCMCPFGN_01136 | 1.4e-27 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
HCMCPFGN_01137 | 5.8e-241 | N | Uncharacterized conserved protein (DUF2075) | |||
HCMCPFGN_01138 | 9.2e-35 | mmuP | E | amino acid | ||
HCMCPFGN_01139 | 6.7e-16 | mmuP | E | amino acid | ||
HCMCPFGN_01140 | 6.5e-58 | steT | E | amino acid | ||
HCMCPFGN_01141 | 7.8e-61 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
HCMCPFGN_01142 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HCMCPFGN_01143 | 2.3e-176 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HCMCPFGN_01144 | 3.6e-302 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
HCMCPFGN_01145 | 0.0 | prtS | 3.4.21.110, 3.4.21.96 | O | Belongs to the peptidase S8 family | |
HCMCPFGN_01146 | 3.1e-159 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HCMCPFGN_01147 | 0.0 | yfjM | S | Protein of unknown function DUF262 | ||
HCMCPFGN_01148 | 1.4e-65 | L | Transposase | |||
HCMCPFGN_01149 | 9.5e-135 | L | Transposase | |||
HCMCPFGN_01152 | 5.4e-200 | L | hmm pf00665 | |||
HCMCPFGN_01153 | 9.5e-116 | L | Helix-turn-helix domain | |||
HCMCPFGN_01154 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
HCMCPFGN_01155 | 1.1e-48 | L | PFAM transposase, IS4 family protein | |||
HCMCPFGN_01156 | 6e-101 | L | PFAM transposase, IS4 family protein | |||
HCMCPFGN_01157 | 0.0 | |||||
HCMCPFGN_01158 | 0.0 | S | PglZ domain | |||
HCMCPFGN_01159 | 1.3e-241 | L | the current gene model (or a revised gene model) may contain a | |||
HCMCPFGN_01160 | 1.7e-277 | V | restriction | |||
HCMCPFGN_01161 | 9.5e-215 | FbpA | 3.1.21.3, 3.2.1.170 | GH38 | K | RNA-binding protein homologous to eukaryotic snRNP |
HCMCPFGN_01162 | 1.5e-109 | S | Domain of unknown function (DUF1788) | |||
HCMCPFGN_01163 | 2.2e-105 | S | Putative inner membrane protein (DUF1819) | |||
HCMCPFGN_01164 | 3.2e-47 | S | Protein of unknown function DUF262 | |||
HCMCPFGN_01165 | 5.1e-180 | S | Protein of unknown function DUF262 | |||
HCMCPFGN_01166 | 5.3e-71 | |||||
HCMCPFGN_01167 | 4.7e-53 | K | Acetyltransferase (GNAT) family | |||
HCMCPFGN_01168 | 2e-109 | rcfA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
HCMCPFGN_01169 | 1e-88 | dps | P | Belongs to the Dps family | ||
HCMCPFGN_01170 | 6e-35 | copZ | C | Heavy-metal-associated domain | ||
HCMCPFGN_01171 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
HCMCPFGN_01172 | 1.7e-49 | mepA | V | MATE efflux family protein | ||
HCMCPFGN_01173 | 1.7e-20 | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | ||
HCMCPFGN_01174 | 1.7e-262 | npr | 1.11.1.1 | C | NADH oxidase | |
HCMCPFGN_01175 | 5.3e-68 | S | pyridoxamine 5-phosphate | |||
HCMCPFGN_01176 | 3.1e-113 | yobV1 | K | WYL domain | ||
HCMCPFGN_01177 | 8.3e-49 | yobV1 | K | WYL domain | ||
HCMCPFGN_01178 | 1.4e-80 | XK26_02160 | S | Pyridoxamine 5'-phosphate oxidase | ||
HCMCPFGN_01179 | 4.7e-31 | |||||
HCMCPFGN_01180 | 2.2e-82 | S | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01181 | 1e-140 | S | Protein of unknown function (DUF3100) | |||
HCMCPFGN_01182 | 5.5e-247 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
HCMCPFGN_01183 | 1.5e-54 | 4.4.1.5 | E | lactoylglutathione lyase activity | ||
HCMCPFGN_01184 | 1.2e-64 | S | ASCH domain | |||
HCMCPFGN_01185 | 2.4e-109 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
HCMCPFGN_01186 | 4.7e-81 | |||||
HCMCPFGN_01187 | 2.1e-304 | |||||
HCMCPFGN_01188 | 2e-97 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
HCMCPFGN_01189 | 1.2e-68 | L | COG3385 FOG Transposase and inactivated derivatives | |||
HCMCPFGN_01190 | 7.5e-108 | V | Transport permease protein | |||
HCMCPFGN_01191 | 2e-124 | V | Transport permease protein | |||
HCMCPFGN_01192 | 1.3e-134 | CP | ATPases associated with a variety of cellular activities | |||
HCMCPFGN_01193 | 1.3e-47 | |||||
HCMCPFGN_01194 | 2.4e-37 | |||||
HCMCPFGN_01195 | 1e-290 | V | ABC transporter transmembrane region | |||
HCMCPFGN_01196 | 9.5e-38 | KLT | serine threonine protein kinase | |||
HCMCPFGN_01197 | 1.8e-290 | V | ABC transporter transmembrane region | |||
HCMCPFGN_01198 | 1.6e-149 | L | Transposase | |||
HCMCPFGN_01199 | 5.2e-91 | S | domain protein | |||
HCMCPFGN_01200 | 2.8e-147 | V | ABC transporter | |||
HCMCPFGN_01201 | 1.9e-74 | S | Protein of unknown function (DUF3021) | |||
HCMCPFGN_01202 | 6.6e-75 | K | LytTr DNA-binding domain | |||
HCMCPFGN_01203 | 6.8e-173 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01204 | 4.8e-24 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01205 | 6.6e-82 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
HCMCPFGN_01208 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
HCMCPFGN_01209 | 6.8e-95 | yyaR | K | Acetyltransferase (GNAT) domain | ||
HCMCPFGN_01210 | 8.6e-38 | mta | K | helix_turn_helix, mercury resistance | ||
HCMCPFGN_01211 | 2.2e-63 | mta | K | helix_turn_helix, mercury resistance | ||
HCMCPFGN_01212 | 6.9e-07 | S | ParE toxin of type II toxin-antitoxin system, parDE | |||
HCMCPFGN_01213 | 1.3e-60 | yyaQ | S | YjbR | ||
HCMCPFGN_01214 | 8.5e-87 | proW | P | ABC transporter, permease protein | ||
HCMCPFGN_01215 | 3.8e-110 | proV | E | ABC transporter, ATP-binding protein | ||
HCMCPFGN_01216 | 7e-89 | proWZ | P | ABC transporter permease | ||
HCMCPFGN_01217 | 4.1e-143 | proX | M | ABC transporter, substrate-binding protein, QAT family | ||
HCMCPFGN_01218 | 6.5e-124 | C | Zinc-binding dehydrogenase | |||
HCMCPFGN_01219 | 5.2e-49 | S | Membrane | |||
HCMCPFGN_01220 | 1.2e-87 | S | Membrane | |||
HCMCPFGN_01221 | 9.3e-25 | I | carboxylic ester hydrolase activity | |||
HCMCPFGN_01222 | 2.9e-62 | 4.2.99.20 | S | Alpha/beta hydrolase family | ||
HCMCPFGN_01223 | 2.2e-32 | S | Biotin synthase | |||
HCMCPFGN_01224 | 1.1e-28 | S | HicB family | |||
HCMCPFGN_01226 | 1.2e-58 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
HCMCPFGN_01227 | 4.6e-45 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
HCMCPFGN_01228 | 4.9e-86 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
HCMCPFGN_01229 | 1.9e-96 | K | Transcriptional regulator, AbiEi antitoxin | |||
HCMCPFGN_01230 | 3.8e-84 | L | Integrase | |||
HCMCPFGN_01231 | 1.9e-115 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01232 | 1.6e-103 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01233 | 1.3e-44 | |||||
HCMCPFGN_01234 | 6.8e-78 | S | Domain of unknown function (DUF5067) | |||
HCMCPFGN_01235 | 4.8e-63 | |||||
HCMCPFGN_01236 | 1.5e-48 | |||||
HCMCPFGN_01237 | 2.6e-143 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HCMCPFGN_01238 | 6.3e-179 | L | Transposase | |||
HCMCPFGN_01239 | 4.5e-264 | lsa | S | ABC transporter | ||
HCMCPFGN_01240 | 1.1e-41 | S | MazG-like family | |||
HCMCPFGN_01241 | 2e-80 | S | AAA domain | |||
HCMCPFGN_01242 | 9.3e-64 | 5.4.2.11 | G | Phosphoglycerate mutase family | ||
HCMCPFGN_01243 | 7.9e-81 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
HCMCPFGN_01244 | 2.1e-119 | XK27_07525 | 3.6.1.55 | F | NUDIX domain | |
HCMCPFGN_01245 | 8.7e-131 | 2.4.2.3 | F | Phosphorylase superfamily | ||
HCMCPFGN_01246 | 1.6e-51 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
HCMCPFGN_01248 | 8e-79 | K | Acetyltransferase (GNAT) domain | |||
HCMCPFGN_01249 | 7.9e-52 | |||||
HCMCPFGN_01250 | 3.5e-219 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01251 | 5.4e-135 | |||||
HCMCPFGN_01252 | 6.1e-208 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_01253 | 1.7e-102 | |||||
HCMCPFGN_01254 | 2.9e-116 | S | Fic/DOC family | |||
HCMCPFGN_01255 | 2.4e-56 | |||||
HCMCPFGN_01256 | 3.3e-78 | |||||
HCMCPFGN_01258 | 1.3e-58 | ypaA | S | Protein of unknown function (DUF1304) | ||
HCMCPFGN_01259 | 9.2e-69 | S | Putative adhesin | |||
HCMCPFGN_01260 | 2.6e-294 | V | ABC-type multidrug transport system, ATPase and permease components | |||
HCMCPFGN_01261 | 9e-295 | P | ABC transporter | |||
HCMCPFGN_01262 | 2.2e-60 | |||||
HCMCPFGN_01263 | 1.4e-29 | fic | D | Fic/DOC family | ||
HCMCPFGN_01264 | 1.9e-33 | |||||
HCMCPFGN_01265 | 1e-256 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
HCMCPFGN_01266 | 1.2e-236 | mepA | V | MATE efflux family protein | ||
HCMCPFGN_01267 | 8.1e-232 | S | Putative peptidoglycan binding domain | |||
HCMCPFGN_01268 | 5.8e-92 | S | ECF-type riboflavin transporter, S component | |||
HCMCPFGN_01269 | 1.2e-149 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
HCMCPFGN_01270 | 2.2e-207 | pbpX1 | V | Beta-lactamase | ||
HCMCPFGN_01271 | 2.7e-106 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
HCMCPFGN_01272 | 1.3e-111 | 3.6.1.27 | I | Acid phosphatase homologues | ||
HCMCPFGN_01273 | 1.7e-78 | C | Flavodoxin | |||
HCMCPFGN_01274 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
HCMCPFGN_01275 | 2.3e-78 | ktrB | P | Potassium uptake protein | ||
HCMCPFGN_01276 | 3e-205 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_01277 | 2.5e-247 | ynbB | 4.4.1.1 | P | aluminum resistance | |
HCMCPFGN_01278 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
HCMCPFGN_01279 | 2.1e-157 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01280 | 3.9e-96 | E | Amino acid permease | |||
HCMCPFGN_01281 | 9.8e-21 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
HCMCPFGN_01282 | 2.5e-170 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01283 | 5.5e-29 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
HCMCPFGN_01284 | 2.9e-63 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HCMCPFGN_01285 | 2.1e-64 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
HCMCPFGN_01286 | 8.4e-243 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_01287 | 3.6e-151 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
HCMCPFGN_01289 | 2.9e-201 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_01290 | 1.6e-176 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
HCMCPFGN_01291 | 1.9e-232 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
HCMCPFGN_01292 | 3e-90 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
HCMCPFGN_01293 | 4.3e-169 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
HCMCPFGN_01294 | 4.4e-247 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
HCMCPFGN_01295 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
HCMCPFGN_01296 | 1.1e-155 | dprA | LU | DNA protecting protein DprA | ||
HCMCPFGN_01297 | 3.7e-134 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HCMCPFGN_01298 | 1.2e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
HCMCPFGN_01299 | 6.8e-279 | yjcE | P | Sodium proton antiporter | ||
HCMCPFGN_01300 | 9.3e-36 | yozE | S | Belongs to the UPF0346 family | ||
HCMCPFGN_01301 | 2.9e-148 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
HCMCPFGN_01302 | 1.5e-113 | hlyIII | S | protein, hemolysin III | ||
HCMCPFGN_01303 | 5.1e-237 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01304 | 3e-205 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_01305 | 7.8e-227 | 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 | |
HCMCPFGN_01306 | 5.2e-159 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
HCMCPFGN_01307 | 1.7e-229 | S | Tetratricopeptide repeat protein | |||
HCMCPFGN_01308 | 3.9e-41 | 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 | ||
HCMCPFGN_01309 | 3.7e-246 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HCMCPFGN_01310 | 9.1e-207 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
HCMCPFGN_01311 | 4.5e-115 | 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 | |
HCMCPFGN_01312 | 3.4e-29 | yocH | M | Lysin motif | ||
HCMCPFGN_01313 | 1.2e-115 | 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 | |||
HCMCPFGN_01314 | 8.5e-128 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HCMCPFGN_01315 | 9.2e-104 | 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 | ||
HCMCPFGN_01316 | 7.2e-130 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
HCMCPFGN_01317 | 4.9e-60 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
HCMCPFGN_01318 | 4e-167 | xerD | D | recombinase XerD | ||
HCMCPFGN_01319 | 5.5e-169 | cvfB | S | S1 domain | ||
HCMCPFGN_01320 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HCMCPFGN_01321 | 2.5e-183 | 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 | |
HCMCPFGN_01322 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
HCMCPFGN_01323 | 2.5e-22 | S | Protein of unknown function (DUF2929) | |||
HCMCPFGN_01324 | 1.5e-307 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
HCMCPFGN_01325 | 7.6e-28 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HCMCPFGN_01326 | 6.2e-33 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
HCMCPFGN_01327 | 6.1e-143 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
HCMCPFGN_01328 | 9.9e-177 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
HCMCPFGN_01329 | 0.0 | oatA | I | Acyltransferase | ||
HCMCPFGN_01330 | 1.4e-242 | 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 | ||
HCMCPFGN_01331 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
HCMCPFGN_01332 | 2.2e-201 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_01333 | 3.2e-10 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
HCMCPFGN_01334 | 2.5e-75 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
HCMCPFGN_01335 | 2.4e-248 | yfnA | E | Amino Acid | ||
HCMCPFGN_01336 | 7.4e-43 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_01337 | 3.4e-78 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_01338 | 3.5e-14 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_01339 | 2.3e-10 | yxeH | S | hydrolase | ||
HCMCPFGN_01340 | 7e-27 | yxeH | S | hydrolase | ||
HCMCPFGN_01341 | 3.4e-86 | yxeH | S | hydrolase | ||
HCMCPFGN_01342 | 1.9e-74 | S | reductase | |||
HCMCPFGN_01343 | 1.2e-35 | S | reductase | |||
HCMCPFGN_01344 | 3e-218 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
HCMCPFGN_01345 | 3.4e-222 | patA | 2.6.1.1 | E | Aminotransferase | |
HCMCPFGN_01346 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
HCMCPFGN_01347 | 8.9e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
HCMCPFGN_01348 | 1.1e-74 | 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 | ||
HCMCPFGN_01349 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
HCMCPFGN_01350 | 8.5e-60 | |||||
HCMCPFGN_01351 | 4.2e-175 | prmA | J | Ribosomal protein L11 methyltransferase | ||
HCMCPFGN_01352 | 3.3e-86 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
HCMCPFGN_01353 | 4.1e-220 | L | Transposase | |||
HCMCPFGN_01354 | 2.2e-232 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01355 | 5.5e-97 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
HCMCPFGN_01356 | 3.1e-248 | yjjP | S | Putative threonine/serine exporter | ||
HCMCPFGN_01357 | 4.7e-174 | citR | K | Putative sugar-binding domain | ||
HCMCPFGN_01358 | 2.7e-51 | |||||
HCMCPFGN_01359 | 4.7e-16 | |||||
HCMCPFGN_01360 | 1.1e-65 | S | Domain of unknown function DUF1828 | |||
HCMCPFGN_01361 | 3.1e-93 | S | UPF0397 protein | |||
HCMCPFGN_01362 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
HCMCPFGN_01363 | 8e-146 | cbiQ | P | cobalt transport | ||
HCMCPFGN_01364 | 1e-09 | |||||
HCMCPFGN_01365 | 1.3e-70 | yeaL | S | Protein of unknown function (DUF441) | ||
HCMCPFGN_01366 | 8.4e-77 | M1-431 | S | Protein of unknown function (DUF1706) | ||
HCMCPFGN_01367 | 2.8e-91 | |||||
HCMCPFGN_01368 | 2.4e-289 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
HCMCPFGN_01369 | 8.2e-168 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
HCMCPFGN_01370 | 9.1e-44 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
HCMCPFGN_01371 | 7.4e-197 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
HCMCPFGN_01372 | 7.6e-154 | ydjP | I | Alpha/beta hydrolase family | ||
HCMCPFGN_01373 | 4.4e-272 | P | Sodium:sulfate symporter transmembrane region | |||
HCMCPFGN_01374 | 1.6e-257 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
HCMCPFGN_01375 | 1.3e-47 | |||||
HCMCPFGN_01376 | 2.1e-43 | |||||
HCMCPFGN_01377 | 6.4e-74 | fhaB | M | Rib/alpha-like repeat | ||
HCMCPFGN_01378 | 1.1e-167 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HCMCPFGN_01380 | 2.2e-16 | 3.5.1.28 | UW | LPXTG-motif cell wall anchor domain protein | ||
HCMCPFGN_01381 | 2.8e-19 | UW | LPXTG-motif cell wall anchor domain protein | |||
HCMCPFGN_01382 | 1.6e-263 | frdC | 1.3.5.4 | C | FAD binding domain | |
HCMCPFGN_01383 | 9e-267 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
HCMCPFGN_01384 | 1.7e-34 | |||||
HCMCPFGN_01385 | 1.9e-188 | S | cog cog1373 | |||
HCMCPFGN_01386 | 5.4e-87 | metI | P | ABC transporter permease | ||
HCMCPFGN_01387 | 5.7e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HCMCPFGN_01388 | 8.2e-162 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
HCMCPFGN_01389 | 0.0 | aha1 | P | E1-E2 ATPase | ||
HCMCPFGN_01390 | 7.2e-16 | ps301 | K | sequence-specific DNA binding | ||
HCMCPFGN_01391 | 2.4e-95 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
HCMCPFGN_01392 | 5.7e-188 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
HCMCPFGN_01393 | 2.7e-247 | yifK | E | Amino acid permease | ||
HCMCPFGN_01394 | 1e-57 | S | PFAM Uncharacterised protein family UPF0150 | |||
HCMCPFGN_01396 | 1e-123 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HCMCPFGN_01397 | 2.5e-31 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
HCMCPFGN_01398 | 2.3e-99 | 3.6.1.27 | I | Acid phosphatase homologues | ||
HCMCPFGN_01399 | 1.5e-131 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
HCMCPFGN_01400 | 1.2e-244 | 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 | |
HCMCPFGN_01401 | 1.7e-65 | S | Domain of unknown function (DUF4767) | |||
HCMCPFGN_01402 | 2e-227 | L | Transposase | |||
HCMCPFGN_01403 | 1.6e-85 | C | nitroreductase | |||
HCMCPFGN_01404 | 5e-10 | ypbG | 2.7.1.2 | GK | ROK family | |
HCMCPFGN_01405 | 2e-80 | ypbG | 2.7.1.2 | GK | ROK family | |
HCMCPFGN_01406 | 2.7e-279 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HCMCPFGN_01407 | 1.1e-106 | lacE | 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 | ||
HCMCPFGN_01408 | 3.4e-84 | pts23C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
HCMCPFGN_01409 | 7.2e-135 | gmuR | K | UTRA | ||
HCMCPFGN_01410 | 6.7e-125 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
HCMCPFGN_01411 | 1.7e-76 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01412 | 4.2e-43 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01413 | 4.9e-116 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01414 | 2.1e-72 | S | Iron-sulphur cluster biosynthesis | |||
HCMCPFGN_01416 | 5.4e-127 | 3.6.1.13, 3.6.1.55 | F | NUDIX domain | ||
HCMCPFGN_01417 | 1.1e-267 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HCMCPFGN_01418 | 7.5e-108 | pncA | Q | Isochorismatase family | ||
HCMCPFGN_01419 | 6.8e-25 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
HCMCPFGN_01420 | 8.8e-144 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
HCMCPFGN_01422 | 3.9e-116 | K | UTRA domain | |||
HCMCPFGN_01423 | 1.3e-289 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HCMCPFGN_01424 | 1.1e-42 | S | Aldo keto reductase | |||
HCMCPFGN_01425 | 9.9e-113 | S | Aldo keto reductase | |||
HCMCPFGN_01426 | 1e-173 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
HCMCPFGN_01427 | 6.1e-55 | |||||
HCMCPFGN_01428 | 8.3e-36 | C | FMN_bind | |||
HCMCPFGN_01429 | 3.2e-300 | I | Protein of unknown function (DUF2974) | |||
HCMCPFGN_01430 | 5.3e-110 | 3.6.1.55 | F | NUDIX domain | ||
HCMCPFGN_01431 | 9.1e-206 | pbpX1 | V | Beta-lactamase | ||
HCMCPFGN_01432 | 1.5e-197 | 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 | |
HCMCPFGN_01433 | 1.8e-212 | aspC | 2.6.1.1 | E | Aminotransferase | |
HCMCPFGN_01434 | 8.6e-142 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
HCMCPFGN_01435 | 2.7e-174 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HCMCPFGN_01436 | 4e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HCMCPFGN_01437 | 3.6e-78 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HCMCPFGN_01438 | 1.4e-248 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HCMCPFGN_01439 | 4.2e-261 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
HCMCPFGN_01440 | 9.2e-189 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
HCMCPFGN_01441 | 2e-272 | yjeM | E | Amino Acid | ||
HCMCPFGN_01442 | 5.4e-104 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HCMCPFGN_01443 | 4.5e-233 | 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 | ||
HCMCPFGN_01444 | 1.5e-207 | 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 | ||
HCMCPFGN_01445 | 4.7e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HCMCPFGN_01446 | 2.4e-150 | |||||
HCMCPFGN_01447 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HCMCPFGN_01448 | 7e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
HCMCPFGN_01449 | 1.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
HCMCPFGN_01450 | 4.8e-174 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
HCMCPFGN_01451 | 0.0 | comEC | S | Competence protein ComEC | ||
HCMCPFGN_01452 | 6.2e-83 | comEA | L | Competence protein ComEA | ||
HCMCPFGN_01453 | 1.4e-192 | ylbL | T | Belongs to the peptidase S16 family | ||
HCMCPFGN_01454 | 2.7e-85 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HCMCPFGN_01455 | 3.2e-95 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
HCMCPFGN_01456 | 8.7e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
HCMCPFGN_01457 | 1.5e-206 | ftsW | D | Belongs to the SEDS family | ||
HCMCPFGN_01458 | 0.0 | typA | T | GTP-binding protein TypA | ||
HCMCPFGN_01459 | 1.7e-99 | 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 | |
HCMCPFGN_01460 | 4.2e-33 | ykzG | S | Belongs to the UPF0356 family | ||
HCMCPFGN_01461 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
HCMCPFGN_01462 | 1.7e-27 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
HCMCPFGN_01463 | 5.9e-106 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
HCMCPFGN_01464 | 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 | |
HCMCPFGN_01465 | 1e-79 | S | Repeat protein | |||
HCMCPFGN_01466 | 7.3e-126 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
HCMCPFGN_01467 | 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 | |
HCMCPFGN_01468 | 4.1e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
HCMCPFGN_01469 | 3.5e-216 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
HCMCPFGN_01470 | 2.5e-124 | 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 | |
HCMCPFGN_01471 | 2.1e-38 | |||||
HCMCPFGN_01472 | 4.4e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
HCMCPFGN_01473 | 2.1e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
HCMCPFGN_01474 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
HCMCPFGN_01475 | 3e-73 | gpsB | D | DivIVA domain protein | ||
HCMCPFGN_01476 | 2.2e-148 | ylmH | S | S4 domain protein | ||
HCMCPFGN_01477 | 9e-47 | yggT | S | YGGT family | ||
HCMCPFGN_01478 | 4.8e-73 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
HCMCPFGN_01479 | 1.6e-204 | 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 | ||
HCMCPFGN_01480 | 2.6e-234 | 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 | ||
HCMCPFGN_01481 | 3.4e-131 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
HCMCPFGN_01482 | 8e-210 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
HCMCPFGN_01483 | 4.7e-260 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
HCMCPFGN_01484 | 7.1e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HCMCPFGN_01485 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
HCMCPFGN_01486 | 9.1e-54 | ftsL | D | Cell division protein FtsL | ||
HCMCPFGN_01487 | 3.3e-183 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
HCMCPFGN_01488 | 9.1e-77 | mraZ | K | Belongs to the MraZ family | ||
HCMCPFGN_01489 | 2.2e-54 | S | Protein of unknown function (DUF3397) | |||
HCMCPFGN_01490 | 6.5e-13 | S | Protein of unknown function (DUF4044) | |||
HCMCPFGN_01491 | 1.1e-95 | mreD | ||||
HCMCPFGN_01492 | 6.7e-148 | mreC | M | Involved in formation and maintenance of cell shape | ||
HCMCPFGN_01493 | 4.2e-173 | mreB | D | cell shape determining protein MreB | ||
HCMCPFGN_01494 | 2.1e-114 | radC | L | DNA repair protein | ||
HCMCPFGN_01495 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
HCMCPFGN_01496 | 3e-237 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
HCMCPFGN_01497 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
HCMCPFGN_01498 | 8.1e-97 | |||||
HCMCPFGN_01499 | 9.5e-92 | S | Bacterial membrane protein, YfhO | |||
HCMCPFGN_01500 | 2.3e-172 | S | Bacterial membrane protein, YfhO | |||
HCMCPFGN_01501 | 1.4e-170 | yfdH | GT2 | M | Glycosyltransferase like family 2 | |
HCMCPFGN_01502 | 2.4e-66 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
HCMCPFGN_01503 | 4.7e-210 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | ||
HCMCPFGN_01504 | 3e-223 | L | Transposase | |||
HCMCPFGN_01507 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
HCMCPFGN_01508 | 8.8e-178 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_01509 | 6.9e-142 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_01510 | 2.7e-17 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_01511 | 1.7e-121 | |||||
HCMCPFGN_01513 | 5.1e-83 | S | Protein of unknown function (DUF3232) | |||
HCMCPFGN_01514 | 6.5e-307 | S | SLAP domain | |||
HCMCPFGN_01515 | 4.4e-132 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_01516 | 1.1e-89 | |||||
HCMCPFGN_01517 | 4.2e-19 | |||||
HCMCPFGN_01518 | 3.9e-66 | |||||
HCMCPFGN_01519 | 2e-14 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_01520 | 4.9e-128 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HCMCPFGN_01521 | 2.5e-142 | K | Helix-turn-helix domain | |||
HCMCPFGN_01522 | 1.7e-229 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
HCMCPFGN_01523 | 8.4e-218 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
HCMCPFGN_01524 | 3.2e-282 | 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 | ||
HCMCPFGN_01525 | 1.8e-110 | 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 | ||
HCMCPFGN_01526 | 2.7e-82 | yueI | S | Protein of unknown function (DUF1694) | ||
HCMCPFGN_01527 | 8e-241 | rarA | L | recombination factor protein RarA | ||
HCMCPFGN_01528 | 2.5e-35 | |||||
HCMCPFGN_01529 | 4e-78 | usp6 | T | universal stress protein | ||
HCMCPFGN_01530 | 3.1e-215 | rodA | D | Belongs to the SEDS family | ||
HCMCPFGN_01531 | 8.6e-34 | S | Protein of unknown function (DUF2969) | |||
HCMCPFGN_01532 | 3.8e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
HCMCPFGN_01533 | 1.9e-178 | mbl | D | Cell shape determining protein MreB Mrl | ||
HCMCPFGN_01534 | 1.9e-28 | ywzB | S | Protein of unknown function (DUF1146) | ||
HCMCPFGN_01535 | 2.2e-52 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HCMCPFGN_01536 | 1.3e-233 | 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 | |
HCMCPFGN_01537 | 1.2e-169 | 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 | ||
HCMCPFGN_01538 | 2.2e-282 | 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 | |
HCMCPFGN_01539 | 6.8e-93 | 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 | ||
HCMCPFGN_01540 | 7.3e-49 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HCMCPFGN_01541 | 3.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
HCMCPFGN_01542 | 3.8e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HCMCPFGN_01543 | 2e-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 | |
HCMCPFGN_01544 | 1.9e-189 | 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 | |
HCMCPFGN_01545 | 3.3e-155 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
HCMCPFGN_01546 | 6.9e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HCMCPFGN_01547 | 2.2e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
HCMCPFGN_01548 | 1.8e-248 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
HCMCPFGN_01551 | 4.6e-196 | ampC | V | Beta-lactamase | ||
HCMCPFGN_01552 | 7.7e-227 | L | Transposase | |||
HCMCPFGN_01553 | 4.4e-41 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_01554 | 1.1e-154 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_01555 | 3.3e-228 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01556 | 1.7e-205 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_01557 | 2.1e-260 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HCMCPFGN_01558 | 8.3e-108 | vanZ | V | VanZ like family | ||
HCMCPFGN_01559 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
HCMCPFGN_01560 | 2.2e-162 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01561 | 4.1e-270 | yclK | 2.7.13.3 | T | Histidine kinase | |
HCMCPFGN_01562 | 1.6e-129 | K | Transcriptional regulatory protein, C terminal | |||
HCMCPFGN_01563 | 2.4e-60 | S | SdpI/YhfL protein family | |||
HCMCPFGN_01564 | 1.1e-167 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
HCMCPFGN_01565 | 2.4e-225 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
HCMCPFGN_01566 | 2.1e-32 | M | Protein of unknown function (DUF3737) | |||
HCMCPFGN_01567 | 2.4e-34 | M | Protein of unknown function (DUF3737) | |||
HCMCPFGN_01569 | 6.8e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HCMCPFGN_01570 | 3.9e-187 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
HCMCPFGN_01571 | 8.4e-82 | comGF | U | Putative Competence protein ComGF | ||
HCMCPFGN_01572 | 1e-41 | |||||
HCMCPFGN_01573 | 2.1e-73 | |||||
HCMCPFGN_01574 | 3.7e-44 | comGC | U | competence protein ComGC | ||
HCMCPFGN_01575 | 7.6e-175 | comGB | NU | type II secretion system | ||
HCMCPFGN_01576 | 2.7e-177 | comGA | NU | Type II IV secretion system protein | ||
HCMCPFGN_01577 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
HCMCPFGN_01578 | 4.6e-91 | S | VanZ like family | |||
HCMCPFGN_01579 | 1.6e-216 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01580 | 5.5e-281 | E | Amino acid permease | |||
HCMCPFGN_01581 | 1.1e-183 | D | Alpha beta | |||
HCMCPFGN_01582 | 1.5e-238 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
HCMCPFGN_01583 | 1.3e-22 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
HCMCPFGN_01584 | 0.0 | bglP | G | phosphotransferase system | ||
HCMCPFGN_01585 | 4.9e-143 | licT | K | CAT RNA binding domain | ||
HCMCPFGN_01586 | 5.2e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
HCMCPFGN_01587 | 1.5e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HCMCPFGN_01588 | 1.8e-117 | |||||
HCMCPFGN_01589 | 3.8e-148 | S | Sucrose-6F-phosphate phosphohydrolase | |||
HCMCPFGN_01590 | 2.6e-149 | S | hydrolase | |||
HCMCPFGN_01591 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
HCMCPFGN_01592 | 1.4e-170 | ybbR | S | YbbR-like protein | ||
HCMCPFGN_01593 | 1.2e-149 | 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 | |
HCMCPFGN_01594 | 4.4e-205 | potD | P | ABC transporter | ||
HCMCPFGN_01595 | 6.5e-124 | potC | P | ABC transporter permease | ||
HCMCPFGN_01596 | 1.3e-129 | potB | P | ABC transporter permease | ||
HCMCPFGN_01597 | 2.9e-204 | 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 | |
HCMCPFGN_01598 | 4.6e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
HCMCPFGN_01599 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
HCMCPFGN_01600 | 2.7e-88 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
HCMCPFGN_01601 | 5.3e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
HCMCPFGN_01602 | 3.3e-137 | 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 | |
HCMCPFGN_01603 | 4.8e-157 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
HCMCPFGN_01604 | 1.8e-95 | |||||
HCMCPFGN_01605 | 7.6e-143 | 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) | |
HCMCPFGN_01606 | 9.3e-228 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
HCMCPFGN_01607 | 8.4e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HCMCPFGN_01608 | 1.2e-188 | cggR | K | Putative sugar-binding domain | ||
HCMCPFGN_01610 | 2.6e-76 | |||||
HCMCPFGN_01611 | 1.7e-166 | |||||
HCMCPFGN_01612 | 3.1e-270 | ycaM | E | amino acid | ||
HCMCPFGN_01613 | 1.5e-133 | S | haloacid dehalogenase-like hydrolase | |||
HCMCPFGN_01614 | 0.0 | S | SH3-like domain | |||
HCMCPFGN_01615 | 1.3e-221 | L | Transposase | |||
HCMCPFGN_01616 | 8.8e-262 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_01617 | 2.3e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
HCMCPFGN_01618 | 4.9e-232 | L | COG2963 Transposase and inactivated derivatives | |||
HCMCPFGN_01619 | 1.1e-170 | whiA | K | May be required for sporulation | ||
HCMCPFGN_01620 | 4.4e-194 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
HCMCPFGN_01621 | 1.8e-164 | rapZ | S | Displays ATPase and GTPase activities | ||
HCMCPFGN_01622 | 1.3e-80 | S | Short repeat of unknown function (DUF308) | |||
HCMCPFGN_01623 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
HCMCPFGN_01624 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
HCMCPFGN_01625 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
HCMCPFGN_01626 | 8.9e-55 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
HCMCPFGN_01627 | 3e-187 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
HCMCPFGN_01628 | 2e-157 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HCMCPFGN_01629 | 3.7e-179 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
HCMCPFGN_01630 | 8.4e-23 | |||||
HCMCPFGN_01631 | 9.5e-186 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
HCMCPFGN_01632 | 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 | ||
HCMCPFGN_01633 | 9.4e-95 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
HCMCPFGN_01634 | 1.7e-133 | comFC | S | Competence protein | ||
HCMCPFGN_01635 | 2.3e-245 | comFA | L | Helicase C-terminal domain protein | ||
HCMCPFGN_01636 | 6.2e-117 | yvyE | 3.4.13.9 | S | YigZ family | |
HCMCPFGN_01637 | 2.4e-209 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
HCMCPFGN_01638 | 3.1e-218 | rny | S | Endoribonuclease that initiates mRNA decay | ||
HCMCPFGN_01639 | 3.6e-194 | 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 | ||
HCMCPFGN_01640 | 1.9e-98 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
HCMCPFGN_01641 | 7.2e-134 | ymfM | S | Helix-turn-helix domain | ||
HCMCPFGN_01642 | 5.2e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HCMCPFGN_01643 | 4.8e-235 | S | Peptidase M16 | |||
HCMCPFGN_01644 | 4.3e-225 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
HCMCPFGN_01645 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
HCMCPFGN_01646 | 1.4e-68 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
HCMCPFGN_01647 | 1.6e-105 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
HCMCPFGN_01648 | 1.9e-212 | yubA | S | AI-2E family transporter | ||
HCMCPFGN_01649 | 2.4e-65 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
HCMCPFGN_01650 | 0.0 | pacL | 3.6.3.8, 3.6.3.9 | P | Cation transporter/ATPase, N-terminus | |
HCMCPFGN_01651 | 5.7e-202 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
HCMCPFGN_01652 | 3.7e-37 | S | SNARE associated Golgi protein | |||
HCMCPFGN_01653 | 1.3e-29 | S | SNARE associated Golgi protein | |||
HCMCPFGN_01654 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
HCMCPFGN_01655 | 2.5e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HCMCPFGN_01656 | 2.7e-154 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
HCMCPFGN_01657 | 2.3e-113 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
HCMCPFGN_01658 | 1.1e-112 | yjbK | S | CYTH | ||
HCMCPFGN_01659 | 2.8e-111 | yjbH | Q | Thioredoxin | ||
HCMCPFGN_01660 | 1.5e-158 | coiA | 3.6.4.12 | S | Competence protein | |
HCMCPFGN_01661 | 7.6e-132 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HCMCPFGN_01662 | 7.9e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
HCMCPFGN_01663 | 9.3e-306 | 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) | |
HCMCPFGN_01664 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
HCMCPFGN_01665 | 2.4e-26 | |||||
HCMCPFGN_01666 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
HCMCPFGN_01667 | 3.9e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
HCMCPFGN_01668 | 3.2e-305 | 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 | ||
HCMCPFGN_01669 | 1.3e-159 | hlyX | S | Transporter associated domain | ||
HCMCPFGN_01670 | 1.3e-73 | |||||
HCMCPFGN_01671 | 1.9e-86 | |||||
HCMCPFGN_01672 | 4.7e-143 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HCMCPFGN_01673 | 3.3e-261 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HCMCPFGN_01674 | 2.8e-98 | D | Alpha beta | |||
HCMCPFGN_01679 | 1.4e-98 | L | Transposase | |||
HCMCPFGN_01680 | 3.2e-77 | L | Transposase | |||
HCMCPFGN_01681 | 5.9e-74 | KLT | Protein kinase domain | |||
HCMCPFGN_01682 | 1.1e-95 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01683 | 7.7e-19 | D | Alpha beta | |||
HCMCPFGN_01684 | 4.2e-46 | |||||
HCMCPFGN_01685 | 1.8e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
HCMCPFGN_01686 | 3.3e-217 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
HCMCPFGN_01687 | 4.6e-216 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
HCMCPFGN_01688 | 5.9e-74 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01689 | 4.9e-98 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01690 | 5.2e-15 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01691 | 1.2e-166 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HCMCPFGN_01692 | 8.3e-152 | yihY | S | Belongs to the UPF0761 family | ||
HCMCPFGN_01693 | 1.9e-163 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
HCMCPFGN_01694 | 1.6e-79 | fld | C | Flavodoxin | ||
HCMCPFGN_01695 | 1.8e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
HCMCPFGN_01696 | 5e-215 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
HCMCPFGN_01697 | 2.7e-25 | |||||
HCMCPFGN_01699 | 3.9e-243 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
HCMCPFGN_01700 | 3.7e-208 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
HCMCPFGN_01701 | 6.4e-128 | M | Glycosyl hydrolases family 25 | |||
HCMCPFGN_01702 | 1.7e-216 | potE | E | amino acid | ||
HCMCPFGN_01703 | 2.2e-102 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HCMCPFGN_01704 | 5e-238 | yhdP | S | Transporter associated domain | ||
HCMCPFGN_01705 | 1.5e-30 | C | nitroreductase | |||
HCMCPFGN_01706 | 1.5e-14 | C | nitroreductase | |||
HCMCPFGN_01707 | 1.6e-39 | |||||
HCMCPFGN_01708 | 4.2e-86 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
HCMCPFGN_01709 | 1.9e-73 | |||||
HCMCPFGN_01710 | 1.8e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
HCMCPFGN_01711 | 0.0 | glvC | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
HCMCPFGN_01712 | 2.2e-86 | S | hydrolase | |||
HCMCPFGN_01713 | 3.3e-11 | 2.7.13.3 | T | GHKL domain | ||
HCMCPFGN_01714 | 2.6e-160 | rssA | S | Phospholipase, patatin family | ||
HCMCPFGN_01715 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
HCMCPFGN_01716 | 1.4e-131 | glcR | K | DeoR C terminal sensor domain | ||
HCMCPFGN_01717 | 5.4e-62 | S | Enterocin A Immunity | |||
HCMCPFGN_01718 | 6.2e-54 | yitW | S | Iron-sulfur cluster assembly protein | ||
HCMCPFGN_01719 | 1.9e-272 | sufB | O | assembly protein SufB | ||
HCMCPFGN_01720 | 4.2e-80 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HCMCPFGN_01721 | 1.5e-236 | 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 | |
HCMCPFGN_01722 | 3.2e-226 | sufD | O | FeS assembly protein SufD | ||
HCMCPFGN_01723 | 1e-145 | sufC | O | FeS assembly ATPase SufC | ||
HCMCPFGN_01724 | 1.5e-95 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01725 | 3e-153 | S | hydrolase | |||
HCMCPFGN_01726 | 3.8e-54 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
HCMCPFGN_01727 | 3.3e-62 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
HCMCPFGN_01728 | 3.7e-17 | ropB | K | Helix-turn-helix domain | ||
HCMCPFGN_01729 | 5.7e-132 | gntR | K | UbiC transcription regulator-associated domain protein | ||
HCMCPFGN_01730 | 4.8e-176 | rihB | 3.2.2.1 | F | Nucleoside | |
HCMCPFGN_01731 | 0.0 | kup | P | Transport of potassium into the cell | ||
HCMCPFGN_01732 | 2.6e-126 | 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 | |
HCMCPFGN_01733 | 5.9e-166 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
HCMCPFGN_01734 | 3.2e-160 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
HCMCPFGN_01735 | 1.6e-233 | G | Bacterial extracellular solute-binding protein | |||
HCMCPFGN_01736 | 2.7e-60 | S | Bacteriocin helveticin-J | |||
HCMCPFGN_01737 | 2.9e-165 | S | SLAP domain | |||
HCMCPFGN_01738 | 1.5e-130 | K | sequence-specific DNA binding | |||
HCMCPFGN_01739 | 2.4e-151 | S | Protein of unknown function (DUF2974) | |||
HCMCPFGN_01740 | 2.2e-106 | glnP | P | ABC transporter permease | ||
HCMCPFGN_01741 | 1.5e-107 | gluC | P | ABC transporter permease | ||
HCMCPFGN_01742 | 4e-150 | glnH | ET | ABC transporter substrate-binding protein | ||
HCMCPFGN_01743 | 1e-131 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
HCMCPFGN_01744 | 1.1e-90 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01745 | 3.2e-96 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01746 | 2.1e-16 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01747 | 2e-85 | tlpA2 | L | Transposase IS200 like | ||
HCMCPFGN_01748 | 1.9e-18 | udk | 2.7.1.48 | F | Zeta toxin | |
HCMCPFGN_01749 | 1.3e-81 | udk | 2.7.1.48 | F | Zeta toxin | |
HCMCPFGN_01750 | 4.2e-63 | EGP | Major facilitator superfamily | |||
HCMCPFGN_01751 | 2.2e-94 | EGP | Major facilitator superfamily | |||
HCMCPFGN_01752 | 2.4e-101 | S | ABC-type cobalt transport system, permease component | |||
HCMCPFGN_01753 | 0.0 | V | ABC transporter transmembrane region | |||
HCMCPFGN_01754 | 5e-291 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
HCMCPFGN_01755 | 2.2e-79 | K | Transcriptional regulator, MarR family | |||
HCMCPFGN_01756 | 5.5e-147 | glnH | ET | ABC transporter | ||
HCMCPFGN_01757 | 4.9e-130 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
HCMCPFGN_01758 | 9.9e-146 | |||||
HCMCPFGN_01759 | 5.8e-310 | ybiT | S | ABC transporter, ATP-binding protein | ||
HCMCPFGN_01760 | 7.8e-210 | pepA | E | M42 glutamyl aminopeptidase | ||
HCMCPFGN_01761 | 5.7e-33 | mdtG | EGP | Major facilitator Superfamily | ||
HCMCPFGN_01762 | 8.6e-168 | mdtG | EGP | Major facilitator Superfamily | ||
HCMCPFGN_01763 | 4e-257 | emrY | EGP | Major facilitator Superfamily | ||
HCMCPFGN_01764 | 7.5e-89 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HCMCPFGN_01765 | 1.7e-238 | pyrP | F | Permease | ||
HCMCPFGN_01766 | 7.3e-155 | S | reductase | |||
HCMCPFGN_01767 | 1.7e-29 | 2.7.1.191 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system | ||
HCMCPFGN_01768 | 9.5e-78 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
HCMCPFGN_01769 | 4e-73 | G | PTS system sorbose-specific iic component | |||
HCMCPFGN_01770 | 3.4e-41 | G | PTS system sorbose-specific iic component | |||
HCMCPFGN_01771 | 3.3e-144 | G | PTS system mannose/fructose/sorbose family IID component | |||
HCMCPFGN_01772 | 9.9e-85 | 2.3.1.128 | K | acetyltransferase | ||
HCMCPFGN_01773 | 3.5e-154 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
HCMCPFGN_01774 | 6.7e-165 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
HCMCPFGN_01775 | 9.1e-92 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
HCMCPFGN_01776 | 1.6e-242 | emrY | EGP | Major facilitator Superfamily | ||
HCMCPFGN_01781 | 2.1e-96 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
HCMCPFGN_01782 | 2.8e-61 | |||||
HCMCPFGN_01783 | 8.7e-116 | L | helicase activity | |||
HCMCPFGN_01785 | 1.2e-227 | L | Transposase | |||
HCMCPFGN_01787 | 1.6e-28 | cspA | K | Cold shock protein | ||
HCMCPFGN_01788 | 3e-259 | tnp2 | L | PFAM Transposase, IS204 IS1001 IS1096 IS1165 | ||
HCMCPFGN_01789 | 1.4e-170 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
HCMCPFGN_01790 | 1.5e-258 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HCMCPFGN_01791 | 2.1e-247 | nhaC | C | Na H antiporter NhaC | ||
HCMCPFGN_01792 | 3.5e-55 | |||||
HCMCPFGN_01793 | 1.1e-119 | ybhL | S | Belongs to the BI1 family | ||
HCMCPFGN_01794 | 4.7e-115 | S | Protein of unknown function (DUF1211) | |||
HCMCPFGN_01795 | 3e-170 | yegS | 2.7.1.107 | G | Lipid kinase | |
HCMCPFGN_01796 | 2.9e-276 | 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) | |
HCMCPFGN_01797 | 2.2e-260 | 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) | |
HCMCPFGN_01798 | 5.2e-50 | 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) | |
HCMCPFGN_01799 | 3e-207 | camS | S | sex pheromone | ||
HCMCPFGN_01800 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
HCMCPFGN_01801 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
HCMCPFGN_01802 | 2e-104 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
HCMCPFGN_01804 | 1.1e-86 | ydcK | S | Belongs to the SprT family | ||
HCMCPFGN_01805 | 1.7e-136 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
HCMCPFGN_01806 | 2.4e-259 | epsU | S | Polysaccharide biosynthesis protein | ||
HCMCPFGN_01807 | 2.1e-224 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
HCMCPFGN_01808 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
HCMCPFGN_01809 | 4.8e-57 | pacL | 3.6.3.8 | P | P-type ATPase | |
HCMCPFGN_01810 | 6.1e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
HCMCPFGN_01811 | 5.2e-281 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HCMCPFGN_01812 | 5.9e-205 | csaB | M | Glycosyl transferases group 1 | ||
HCMCPFGN_01813 | 5.6e-135 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
HCMCPFGN_01814 | 6.8e-215 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01815 | 1.8e-55 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
HCMCPFGN_01816 | 1.4e-122 | gntR1 | K | UTRA | ||
HCMCPFGN_01817 | 7.8e-213 | |||||
HCMCPFGN_01820 | 1.5e-92 | |||||
HCMCPFGN_01821 | 3.8e-258 | slpX | S | SLAP domain | ||
HCMCPFGN_01822 | 1.3e-114 | pfoS | S | Phosphotransferase system, EIIC | ||
HCMCPFGN_01823 | 1.5e-19 | pfoS | S | Phosphotransferase system, EIIC | ||
HCMCPFGN_01825 | 1.5e-202 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_01826 | 3.2e-132 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
HCMCPFGN_01827 | 8.5e-229 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
HCMCPFGN_01828 | 3.4e-111 | G | Phosphoglycerate mutase family | |||
HCMCPFGN_01829 | 2.8e-196 | D | nuclear chromosome segregation | |||
HCMCPFGN_01830 | 3e-45 | M | LysM domain protein | |||
HCMCPFGN_01831 | 5.6e-13 | |||||
HCMCPFGN_01832 | 1.1e-25 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
HCMCPFGN_01833 | 1.5e-95 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
HCMCPFGN_01834 | 2.1e-67 | |||||
HCMCPFGN_01835 | 7.1e-32 | |||||
HCMCPFGN_01836 | 4.1e-71 | S | Iron-sulphur cluster biosynthesis | |||
HCMCPFGN_01837 | 2.8e-53 | rpiR1 | K | Helix-turn-helix domain, rpiR family | ||
HCMCPFGN_01838 | 3.1e-228 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
HCMCPFGN_01839 | 1.9e-127 | XK27_08435 | K | UTRA | ||
HCMCPFGN_01841 | 1e-71 | C | FAD binding domain | |||
HCMCPFGN_01842 | 3.1e-26 | C | FAD binding domain | |||
HCMCPFGN_01843 | 3e-49 | C | FAD binding domain | |||
HCMCPFGN_01844 | 1.1e-14 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
HCMCPFGN_01845 | 2.9e-139 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
HCMCPFGN_01846 | 5.1e-60 | |||||
HCMCPFGN_01847 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
HCMCPFGN_01848 | 2.3e-251 | P | P-loop Domain of unknown function (DUF2791) | |||
HCMCPFGN_01849 | 7.7e-258 | S | TerB-C domain | |||
HCMCPFGN_01850 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
HCMCPFGN_01851 | 1.4e-256 | L | Probable transposase | |||
HCMCPFGN_01852 | 7.8e-106 | L | Resolvase, N terminal domain | |||
HCMCPFGN_01853 | 7.7e-73 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
HCMCPFGN_01854 | 6.4e-37 | |||||
HCMCPFGN_01855 | 3.9e-136 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
HCMCPFGN_01856 | 4e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HCMCPFGN_01857 | 2.1e-79 | S | LPXTG cell wall anchor motif | |||
HCMCPFGN_01858 | 3.6e-90 | UW | LPXTG-motif cell wall anchor domain protein | |||
HCMCPFGN_01859 | 1e-72 | |||||
HCMCPFGN_01860 | 1e-102 | yagE | E | amino acid | ||
HCMCPFGN_01861 | 8.8e-47 | |||||
HCMCPFGN_01862 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
HCMCPFGN_01863 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
HCMCPFGN_01864 | 8.6e-238 | cycA | E | Amino acid permease | ||
HCMCPFGN_01865 | 1.4e-82 | maa | S | transferase hexapeptide repeat | ||
HCMCPFGN_01866 | 1.2e-22 | K | Transcriptional regulator | |||
HCMCPFGN_01867 | 2.4e-104 | K | Transcriptional regulator | |||
HCMCPFGN_01868 | 7.6e-64 | manO | S | Domain of unknown function (DUF956) | ||
HCMCPFGN_01869 | 2.2e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
HCMCPFGN_01870 | 3.1e-134 | manY | G | PTS system | ||
HCMCPFGN_01871 | 3e-187 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
HCMCPFGN_01872 | 9.7e-65 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
HCMCPFGN_01873 | 3.5e-112 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
HCMCPFGN_01874 | 1.8e-26 | L | Transposase | |||
HCMCPFGN_01875 | 2.6e-14 | scrA | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
HCMCPFGN_01876 | 3e-216 | scrA | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
HCMCPFGN_01877 | 1.1e-130 | scrB | 3.2.1.26 | GH32 | G | invertase |
HCMCPFGN_01878 | 9.1e-98 | msmR7 | K | helix_turn_helix, arabinose operon control protein | ||
HCMCPFGN_01879 | 3.8e-45 | msmR7 | K | helix_turn_helix, arabinose operon control protein | ||
HCMCPFGN_01881 | 2.4e-83 | S | COG NOG38524 non supervised orthologous group | |||
HCMCPFGN_01884 | 6.5e-77 | |||||
HCMCPFGN_01885 | 2.9e-251 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
HCMCPFGN_01886 | 2.3e-96 | J | Acetyltransferase (GNAT) domain | |||
HCMCPFGN_01887 | 2.8e-108 | yjbF | S | SNARE associated Golgi protein | ||
HCMCPFGN_01888 | 1.3e-153 | I | alpha/beta hydrolase fold | |||
HCMCPFGN_01889 | 1e-08 | hipB | K | Helix-turn-helix | ||
HCMCPFGN_01890 | 1.7e-125 | hipB | K | Helix-turn-helix | ||
HCMCPFGN_01891 | 2.5e-261 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
HCMCPFGN_01892 | 3.3e-149 | |||||
HCMCPFGN_01893 | 0.0 | ydgH | S | MMPL family | ||
HCMCPFGN_01894 | 3.3e-98 | yobS | K | Bacterial regulatory proteins, tetR family | ||
HCMCPFGN_01895 | 1e-157 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
HCMCPFGN_01896 | 5.3e-159 | corA | P | CorA-like Mg2+ transporter protein | ||
HCMCPFGN_01897 | 1.8e-240 | G | Bacterial extracellular solute-binding protein | |||
HCMCPFGN_01898 | 3.5e-257 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
HCMCPFGN_01899 | 4.7e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
HCMCPFGN_01900 | 8e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
HCMCPFGN_01901 | 3.9e-201 | malK | P | ATPases associated with a variety of cellular activities | ||
HCMCPFGN_01902 | 5e-281 | pipD | E | Dipeptidase | ||
HCMCPFGN_01903 | 8.5e-159 | endA | F | DNA RNA non-specific endonuclease | ||
HCMCPFGN_01904 | 1.1e-159 | dnaQ | 2.7.7.7 | L | EXOIII | |
HCMCPFGN_01905 | 7.6e-157 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
HCMCPFGN_01908 | 4.9e-90 | L | Transposase DDE domain | |||
HCMCPFGN_01909 | 3.4e-56 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
HCMCPFGN_01910 | 1.2e-123 | tnp | L | DDE domain | ||
HCMCPFGN_01911 | 1.2e-12 | ytgB | S | Transglycosylase associated protein | ||
HCMCPFGN_01912 | 1.8e-130 | S | Phage Mu protein F like protein | |||
HCMCPFGN_01913 | 8.9e-75 | tnpR | L | Resolvase, N terminal domain | ||
HCMCPFGN_01914 | 2e-13 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
HCMCPFGN_01915 | 1.3e-232 | L | Transposase | |||
HCMCPFGN_01916 | 9.3e-149 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_01917 | 3.2e-69 | S | Membrane transport protein | |||
HCMCPFGN_01918 | 1.3e-156 | L | Integrase core domain | |||
HCMCPFGN_01919 | 2.9e-38 | L | Transposase and inactivated derivatives | |||
HCMCPFGN_01920 | 7.9e-76 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HCMCPFGN_01921 | 4.5e-138 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01922 | 1.3e-51 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01923 | 6.2e-70 | |||||
HCMCPFGN_01924 | 3.9e-44 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
HCMCPFGN_01925 | 5.2e-50 | repA | S | Replication initiator protein A | ||
HCMCPFGN_01926 | 3.2e-71 | repA | S | Replication initiator protein A | ||
HCMCPFGN_01927 | 5.3e-75 | sdrF | M | domain protein | ||
HCMCPFGN_01928 | 1.2e-98 | infB | M | YSIRK type signal peptide | ||
HCMCPFGN_01929 | 4.5e-16 | sdrF | M | domain protein | ||
HCMCPFGN_01930 | 8.4e-139 | pnuC | H | nicotinamide mononucleotide transporter | ||
HCMCPFGN_01931 | 4.1e-11 | |||||
HCMCPFGN_01932 | 3.2e-239 | L | Probable transposase | |||
HCMCPFGN_01933 | 8.8e-215 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01934 | 1.9e-276 | V | ABC transporter transmembrane region | |||
HCMCPFGN_01935 | 9.3e-180 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
HCMCPFGN_01936 | 5.1e-187 | 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 | |
HCMCPFGN_01937 | 1.3e-95 | F | Nucleoside 2-deoxyribosyltransferase | |||
HCMCPFGN_01938 | 2.7e-69 | S | Peptidase propeptide and YPEB domain | |||
HCMCPFGN_01939 | 5.8e-86 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
HCMCPFGN_01940 | 1.4e-67 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
HCMCPFGN_01941 | 7.8e-14 | S | Peptidase propeptide and YPEB domain | |||
HCMCPFGN_01942 | 1.4e-66 | S | Peptidase propeptide and YPEB domain | |||
HCMCPFGN_01943 | 3.1e-245 | G | Bacterial extracellular solute-binding protein | |||
HCMCPFGN_01944 | 1.3e-102 | 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 | ||
HCMCPFGN_01945 | 3.9e-170 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
HCMCPFGN_01946 | 1.1e-103 | E | GDSL-like Lipase/Acylhydrolase | |||
HCMCPFGN_01947 | 5.2e-215 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01948 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
HCMCPFGN_01949 | 1.7e-125 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
HCMCPFGN_01950 | 1.1e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
HCMCPFGN_01951 | 4.8e-202 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_01952 | 2.5e-98 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
HCMCPFGN_01953 | 1.4e-245 | aspT | P | Predicted Permease Membrane Region | ||
HCMCPFGN_01954 | 5.9e-152 | asdA | 4.1.1.12 | E | Aminotransferase | |
HCMCPFGN_01955 | 2.6e-91 | L | Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_01957 | 2.6e-45 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
HCMCPFGN_01958 | 1.3e-16 | |||||
HCMCPFGN_01959 | 1.3e-11 | S | Transglycosylase associated protein | |||
HCMCPFGN_01960 | 1.5e-84 | S | Asp23 family, cell envelope-related function | |||
HCMCPFGN_01961 | 8.1e-22 | S | Small integral membrane protein (DUF2273) | |||
HCMCPFGN_01962 | 1.8e-93 | |||||
HCMCPFGN_01963 | 9.2e-242 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_01964 | 3.4e-50 | asdA | 4.1.1.12 | E | Aminotransferase class I and II | |
HCMCPFGN_01965 | 0.0 | V | FtsX-like permease family | |||
HCMCPFGN_01966 | 2.7e-132 | cysA | V | ABC transporter, ATP-binding protein | ||
HCMCPFGN_01967 | 2.7e-238 | S | response to antibiotic | |||
HCMCPFGN_01968 | 1.4e-124 | |||||
HCMCPFGN_01969 | 1.3e-116 | 3.6.3.8 | P | P-type ATPase | ||
HCMCPFGN_01970 | 3.8e-31 | 3.6.3.8 | P | P-type ATPase | ||
HCMCPFGN_01971 | 1.9e-54 | 3.6.3.8 | P | P-type ATPase | ||
HCMCPFGN_01972 | 1.7e-20 | |||||
HCMCPFGN_01973 | 3.2e-15 | |||||
HCMCPFGN_01974 | 1.7e-187 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
HCMCPFGN_01975 | 3e-131 | glvR | K | Helix-turn-helix domain, rpiR family | ||
HCMCPFGN_01976 | 1.1e-266 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
HCMCPFGN_01977 | 6.7e-41 | |||||
HCMCPFGN_01978 | 1.9e-46 | |||||
HCMCPFGN_01979 | 5.6e-197 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_01980 | 1.1e-92 | |||||
HCMCPFGN_01981 | 2.5e-39 | 3.2.2.20 | K | acetyltransferase | ||
HCMCPFGN_01982 | 2.3e-149 | pbpX2 | V | Beta-lactamase | ||
HCMCPFGN_01983 | 1.2e-238 | L | Probable transposase | |||
HCMCPFGN_01984 | 3.4e-163 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HCMCPFGN_01985 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
HCMCPFGN_01986 | 4.9e-276 | E | Amino acid permease | |||
HCMCPFGN_01987 | 3.1e-228 | L | Transposase | |||
HCMCPFGN_01988 | 4e-140 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
HCMCPFGN_01989 | 4.5e-202 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_01990 | 4.4e-24 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
HCMCPFGN_01991 | 1.3e-247 | S | Membrane protein involved in the export of O-antigen and teichoic acid | |||
HCMCPFGN_01992 | 3.6e-157 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_01993 | 1.6e-177 | lgtD | S | glycosyl transferase family 2 | ||
HCMCPFGN_01994 | 1.9e-196 | |||||
HCMCPFGN_01995 | 1.3e-145 | M | Domain of unknown function (DUF4422) | |||
HCMCPFGN_01996 | 8.3e-210 | GT4 | M | Glycosyl transferases group 1 | ||
HCMCPFGN_01997 | 2.9e-196 | waaB | GT4 | M | Glycosyl transferases group 1 | |
HCMCPFGN_01998 | 8.6e-126 | cps1D | M | Domain of unknown function (DUF4422) | ||
HCMCPFGN_01999 | 2.2e-122 | rfbP | M | Bacterial sugar transferase | ||
HCMCPFGN_02000 | 1.1e-144 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
HCMCPFGN_02001 | 5.1e-118 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
HCMCPFGN_02002 | 2e-139 | epsB | M | biosynthesis protein | ||
HCMCPFGN_02003 | 7e-179 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HCMCPFGN_02004 | 1.7e-200 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
HCMCPFGN_02007 | 2.5e-140 | M | NlpC/P60 family | |||
HCMCPFGN_02008 | 4.7e-124 | M | NlpC P60 family protein | |||
HCMCPFGN_02009 | 8.8e-58 | S | Archaea bacterial proteins of unknown function | |||
HCMCPFGN_02010 | 1.8e-30 | S | Archaea bacterial proteins of unknown function | |||
HCMCPFGN_02011 | 1.1e-93 | M | NlpC/P60 family | |||
HCMCPFGN_02012 | 2.7e-94 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
HCMCPFGN_02013 | 4.3e-25 | |||||
HCMCPFGN_02014 | 1e-279 | S | O-antigen ligase like membrane protein | |||
HCMCPFGN_02015 | 1.2e-219 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02016 | 1.1e-94 | |||||
HCMCPFGN_02017 | 1.2e-74 | nrdI | F | Belongs to the NrdI family | ||
HCMCPFGN_02018 | 9.9e-10 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HCMCPFGN_02019 | 9.2e-21 | |||||
HCMCPFGN_02020 | 1.6e-67 | |||||
HCMCPFGN_02021 | 3.9e-240 | L | Probable transposase | |||
HCMCPFGN_02022 | 1.1e-81 | S | Threonine/Serine exporter, ThrE | |||
HCMCPFGN_02023 | 4.4e-138 | thrE | S | Putative threonine/serine exporter | ||
HCMCPFGN_02024 | 1.3e-287 | S | ABC transporter | |||
HCMCPFGN_02025 | 5e-55 | |||||
HCMCPFGN_02026 | 8.4e-99 | rimL | J | Acetyltransferase (GNAT) domain | ||
HCMCPFGN_02027 | 1.3e-10 | S | Protein of unknown function (DUF554) | |||
HCMCPFGN_02028 | 5.4e-215 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
HCMCPFGN_02029 | 0.0 | pepF | E | oligoendopeptidase F | ||
HCMCPFGN_02030 | 1.1e-22 | Z012_06740 | S | Fic/DOC family | ||
HCMCPFGN_02031 | 5.8e-186 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02032 | 2.1e-42 | S | Enterocin A Immunity | |||
HCMCPFGN_02033 | 3.6e-52 | lctP | C | L-lactate permease | ||
HCMCPFGN_02034 | 3.6e-90 | lctP | C | L-lactate permease | ||
HCMCPFGN_02035 | 5.2e-24 | lctP | C | L-lactate permease | ||
HCMCPFGN_02036 | 4.8e-51 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_02037 | 9.9e-234 | ydjN | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
HCMCPFGN_02038 | 2.6e-130 | znuB | U | ABC 3 transport family | ||
HCMCPFGN_02039 | 1.6e-117 | fhuC | P | ABC transporter | ||
HCMCPFGN_02040 | 4.4e-158 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HCMCPFGN_02041 | 5.1e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
HCMCPFGN_02042 | 2.7e-246 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_02043 | 2e-14 | S | Enterocin A Immunity | |||
HCMCPFGN_02044 | 1.4e-211 | S | Archaea bacterial proteins of unknown function | |||
HCMCPFGN_02045 | 7.2e-146 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
HCMCPFGN_02046 | 3.2e-305 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HCMCPFGN_02047 | 9.2e-209 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
HCMCPFGN_02048 | 5.1e-122 | K | response regulator | |||
HCMCPFGN_02049 | 0.0 | V | ABC transporter | |||
HCMCPFGN_02050 | 4.2e-298 | V | ABC transporter, ATP-binding protein | |||
HCMCPFGN_02051 | 2e-138 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HCMCPFGN_02052 | 6.1e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HCMCPFGN_02053 | 3.7e-44 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
HCMCPFGN_02054 | 8.5e-154 | spo0J | K | Belongs to the ParB family | ||
HCMCPFGN_02055 | 7e-136 | soj | D | Sporulation initiation inhibitor | ||
HCMCPFGN_02056 | 3.9e-148 | noc | K | Belongs to the ParB family | ||
HCMCPFGN_02057 | 1.8e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HCMCPFGN_02058 | 7.3e-84 | cvpA | S | Colicin V production protein | ||
HCMCPFGN_02059 | 3.8e-181 | 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 | |
HCMCPFGN_02060 | 2.8e-148 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
HCMCPFGN_02061 | 3.5e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
HCMCPFGN_02062 | 5.4e-95 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
HCMCPFGN_02063 | 3.1e-110 | K | WHG domain | |||
HCMCPFGN_02064 | 8e-38 | |||||
HCMCPFGN_02065 | 1.5e-274 | pipD | E | Dipeptidase | ||
HCMCPFGN_02066 | 1.2e-118 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
HCMCPFGN_02067 | 2.6e-165 | hrtB | V | ABC transporter permease | ||
HCMCPFGN_02068 | 2.2e-93 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
HCMCPFGN_02069 | 1.8e-110 | G | phosphoglycerate mutase | |||
HCMCPFGN_02070 | 6.6e-139 | aroD | S | Alpha/beta hydrolase family | ||
HCMCPFGN_02071 | 6.4e-142 | S | Belongs to the UPF0246 family | |||
HCMCPFGN_02072 | 1.2e-120 | |||||
HCMCPFGN_02073 | 3.1e-49 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
HCMCPFGN_02074 | 1.5e-214 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02075 | 2.1e-42 | S | Enterocin A Immunity | |||
HCMCPFGN_02076 | 3.6e-52 | lctP | C | L-lactate permease | ||
HCMCPFGN_02077 | 3.6e-90 | lctP | C | L-lactate permease | ||
HCMCPFGN_02078 | 5.2e-24 | lctP | C | L-lactate permease | ||
HCMCPFGN_02079 | 3.8e-145 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_02080 | 1e-72 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_02081 | 1.7e-205 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_02082 | 1.1e-167 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
HCMCPFGN_02083 | 1.8e-136 | fruR | K | DeoR C terminal sensor domain | ||
HCMCPFGN_02086 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
HCMCPFGN_02087 | 5.6e-26 | |||||
HCMCPFGN_02088 | 2.1e-32 | |||||
HCMCPFGN_02089 | 6.6e-34 | yozG | K | Transcriptional regulator | ||
HCMCPFGN_02090 | 2.7e-246 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_02091 | 2e-14 | S | Enterocin A Immunity | |||
HCMCPFGN_02092 | 1.4e-211 | S | Archaea bacterial proteins of unknown function | |||
HCMCPFGN_02093 | 7.2e-146 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
HCMCPFGN_02094 | 3.2e-305 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HCMCPFGN_02095 | 9.2e-209 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
HCMCPFGN_02096 | 5.1e-122 | K | response regulator | |||
HCMCPFGN_02097 | 0.0 | V | ABC transporter | |||
HCMCPFGN_02098 | 4.2e-298 | V | ABC transporter, ATP-binding protein | |||
HCMCPFGN_02099 | 2e-138 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HCMCPFGN_02100 | 6.1e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HCMCPFGN_02101 | 3.7e-44 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
HCMCPFGN_02102 | 8.5e-154 | spo0J | K | Belongs to the ParB family | ||
HCMCPFGN_02103 | 7e-136 | soj | D | Sporulation initiation inhibitor | ||
HCMCPFGN_02104 | 3.9e-148 | noc | K | Belongs to the ParB family | ||
HCMCPFGN_02105 | 1.8e-130 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
HCMCPFGN_02106 | 7.3e-84 | cvpA | S | Colicin V production protein | ||
HCMCPFGN_02107 | 3.8e-181 | 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 | |
HCMCPFGN_02108 | 2.8e-148 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
HCMCPFGN_02109 | 3.5e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
HCMCPFGN_02110 | 5.4e-95 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
HCMCPFGN_02111 | 3.1e-110 | K | WHG domain | |||
HCMCPFGN_02112 | 8e-38 | |||||
HCMCPFGN_02113 | 1.5e-274 | pipD | E | Dipeptidase | ||
HCMCPFGN_02114 | 1.2e-118 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
HCMCPFGN_02115 | 2.6e-165 | hrtB | V | ABC transporter permease | ||
HCMCPFGN_02116 | 2.2e-93 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
HCMCPFGN_02117 | 1.8e-110 | G | phosphoglycerate mutase | |||
HCMCPFGN_02118 | 6.6e-139 | aroD | S | Alpha/beta hydrolase family | ||
HCMCPFGN_02119 | 6.4e-142 | S | Belongs to the UPF0246 family | |||
HCMCPFGN_02120 | 1.2e-120 | |||||
HCMCPFGN_02121 | 3.1e-49 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
HCMCPFGN_02122 | 2.7e-219 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02123 | 1.6e-182 | S | Putative peptidoglycan binding domain | |||
HCMCPFGN_02124 | 1.8e-24 | |||||
HCMCPFGN_02125 | 1e-247 | dtpT | U | amino acid peptide transporter | ||
HCMCPFGN_02126 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
HCMCPFGN_02128 | 1.2e-58 | lysM | M | LysM domain | ||
HCMCPFGN_02129 | 4.8e-166 | |||||
HCMCPFGN_02130 | 1.4e-213 | mdtG | EGP | Major facilitator Superfamily | ||
HCMCPFGN_02131 | 2.1e-74 | L | PFAM transposase, IS4 family protein | |||
HCMCPFGN_02132 | 5e-23 | repA | S | Replication initiator protein A | ||
HCMCPFGN_02133 | 6.7e-34 | L | An automated process has identified a potential problem with this gene model | |||
HCMCPFGN_02134 | 4.4e-08 | ropB | K | Transcriptional regulator | ||
HCMCPFGN_02135 | 3e-208 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_02136 | 5.2e-116 | ropB | K | Transcriptional regulator | ||
HCMCPFGN_02137 | 1.9e-209 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02138 | 1.6e-20 | |||||
HCMCPFGN_02139 | 4.6e-118 | ropB | K | Transcriptional regulator | ||
HCMCPFGN_02140 | 1.4e-226 | L | Transposase | |||
HCMCPFGN_02141 | 7.3e-40 | S | Enterocin A Immunity | |||
HCMCPFGN_02142 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HCMCPFGN_02143 | 1.2e-73 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
HCMCPFGN_02144 | 4.7e-193 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HCMCPFGN_02145 | 1.4e-84 | IQ | reductase | |||
HCMCPFGN_02146 | 7.1e-71 | metQ_4 | P | Belongs to the nlpA lipoprotein family | ||
HCMCPFGN_02147 | 2.2e-160 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_02148 | 2.5e-56 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_02149 | 4.3e-88 | 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) | |
HCMCPFGN_02150 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HCMCPFGN_02151 | 9.2e-167 | metF | 1.5.1.20 | C | Methylenetetrahydrofolate reductase | |
HCMCPFGN_02152 | 2.4e-220 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02153 | 2.6e-194 | L | Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_02154 | 2.8e-183 | P | secondary active sulfate transmembrane transporter activity | |||
HCMCPFGN_02155 | 1.5e-95 | apt | 2.4.2.22, 2.4.2.7 | F | Phosphoribosyl transferase domain | |
HCMCPFGN_02156 | 6.8e-245 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
HCMCPFGN_02157 | 2.8e-54 | bioY | S | BioY family | ||
HCMCPFGN_02158 | 4.1e-189 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HCMCPFGN_02159 | 1.9e-133 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
HCMCPFGN_02160 | 4.1e-144 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
HCMCPFGN_02161 | 6e-157 | 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 | |
HCMCPFGN_02162 | 9.8e-258 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
HCMCPFGN_02163 | 1.7e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
HCMCPFGN_02164 | 3.7e-79 | 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 | |
HCMCPFGN_02165 | 1.3e-229 | 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 | |
HCMCPFGN_02166 | 1.2e-126 | IQ | reductase | |||
HCMCPFGN_02167 | 1.1e-167 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
HCMCPFGN_02168 | 4.9e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HCMCPFGN_02169 | 2.2e-179 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
HCMCPFGN_02170 | 1.1e-78 | marR | K | Transcriptional regulator | ||
HCMCPFGN_02171 | 3.8e-78 | 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 | |
HCMCPFGN_02172 | 1.2e-25 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
HCMCPFGN_02173 | 4.3e-121 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
HCMCPFGN_02174 | 7e-13 | ytgB | S | Transglycosylase associated protein | ||
HCMCPFGN_02175 | 8.2e-179 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_02176 | 4.4e-86 | L | Resolvase, N terminal domain | |||
HCMCPFGN_02177 | 1.3e-232 | L | Transposase | |||
HCMCPFGN_02178 | 1.7e-154 | glcU | U | sugar transport | ||
HCMCPFGN_02179 | 3.5e-163 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_02180 | 0.0 | uvrA2 | L | ABC transporter | ||
HCMCPFGN_02181 | 1.2e-103 | L | HTH-like domain | |||
HCMCPFGN_02182 | 9.5e-92 | L | Helix-turn-helix domain | |||
HCMCPFGN_02183 | 2.4e-223 | oxlT | P | Major Facilitator Superfamily | ||
HCMCPFGN_02185 | 2e-71 | L | Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_02186 | 9.5e-217 | yceI | EGP | Major facilitator Superfamily | ||
HCMCPFGN_02187 | 1.1e-153 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, C-terminal domain | |
HCMCPFGN_02188 | 7e-89 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_02189 | 1.7e-205 | L | COG3547 Transposase and inactivated derivatives | |||
HCMCPFGN_02190 | 4.8e-257 | ykgC | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
HCMCPFGN_02191 | 1.4e-36 | M | Collagen binding domain | |||
HCMCPFGN_02192 | 1.2e-20 | M | Collagen binding domain | |||
HCMCPFGN_02193 | 1.7e-28 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
HCMCPFGN_02194 | 1.3e-33 | ymdB | S | Macro domain protein | ||
HCMCPFGN_02196 | 1.2e-152 | malG | P | ABC transporter permease | ||
HCMCPFGN_02197 | 2e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
HCMCPFGN_02198 | 1.6e-211 | malE | G | Bacterial extracellular solute-binding protein | ||
HCMCPFGN_02199 | 8.3e-207 | msmX | P | Belongs to the ABC transporter superfamily | ||
HCMCPFGN_02200 | 9.7e-118 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
HCMCPFGN_02201 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
HCMCPFGN_02202 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HCMCPFGN_02203 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
HCMCPFGN_02204 | 9.3e-45 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HCMCPFGN_02205 | 8.3e-240 | L | Probable transposase | |||
HCMCPFGN_02206 | 6.6e-111 | ackA | 2.7.2.1 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HCMCPFGN_02207 | 5.5e-175 | yvdE | K | helix_turn _helix lactose operon repressor | ||
HCMCPFGN_02208 | 3e-147 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
HCMCPFGN_02209 | 5.2e-229 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
HCMCPFGN_02210 | 5.6e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
HCMCPFGN_02212 | 7.8e-131 | cobQ | S | glutamine amidotransferase | ||
HCMCPFGN_02213 | 9.5e-83 | M | NlpC/P60 family | |||
HCMCPFGN_02214 | 2.3e-149 | EG | EamA-like transporter family | |||
HCMCPFGN_02215 | 5.5e-110 | |||||
HCMCPFGN_02216 | 6.9e-78 | |||||
HCMCPFGN_02217 | 2.7e-183 | XK27_05540 | S | DUF218 domain | ||
HCMCPFGN_02218 | 2.1e-135 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
HCMCPFGN_02219 | 3.4e-32 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
HCMCPFGN_02220 | 2.9e-84 | |||||
HCMCPFGN_02221 | 6.1e-58 | |||||
HCMCPFGN_02222 | 5.8e-244 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
HCMCPFGN_02223 | 1.6e-246 | 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 | |
HCMCPFGN_02224 | 1.3e-182 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
HCMCPFGN_02227 | 9e-203 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
HCMCPFGN_02228 | 2e-191 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
HCMCPFGN_02229 | 3.8e-106 | steT_1 | E | amino acid | ||
HCMCPFGN_02230 | 1.5e-14 | puuD | S | peptidase C26 | ||
HCMCPFGN_02231 | 1.9e-245 | yifK | E | Amino acid permease | ||
HCMCPFGN_02232 | 3.3e-216 | cycA | E | Amino acid permease | ||
HCMCPFGN_02233 | 4.1e-128 | |||||
HCMCPFGN_02234 | 4.9e-119 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
HCMCPFGN_02235 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
HCMCPFGN_02236 | 1.8e-156 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
HCMCPFGN_02237 | 1.4e-210 | 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 | ||
HCMCPFGN_02238 | 1.9e-124 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
HCMCPFGN_02239 | 2.3e-113 | XK27_06780 | V | ABC transporter permease | ||
HCMCPFGN_02240 | 6.1e-193 | XK27_06780 | V | ABC transporter permease | ||
HCMCPFGN_02241 | 1.2e-35 | |||||
HCMCPFGN_02242 | 3.4e-286 | ytgP | S | Polysaccharide biosynthesis protein | ||
HCMCPFGN_02243 | 3.4e-148 | lysA2 | M | Glycosyl hydrolases family 25 | ||
HCMCPFGN_02244 | 2.5e-121 | S | Protein of unknown function (DUF975) | |||
HCMCPFGN_02245 | 1.8e-32 | |||||
HCMCPFGN_02246 | 1.7e-29 | |||||
HCMCPFGN_02247 | 1.1e-119 | S | CAAX protease self-immunity | |||
HCMCPFGN_02248 | 2e-10 | |||||
HCMCPFGN_02250 | 1.6e-174 | pbpX2 | V | Beta-lactamase | ||
HCMCPFGN_02251 | 2.8e-246 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
HCMCPFGN_02252 | 5.7e-36 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HCMCPFGN_02253 | 3e-242 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
HCMCPFGN_02254 | 1.6e-293 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
HCMCPFGN_02255 | 5.2e-19 | S | D-Ala-teichoic acid biosynthesis protein | |||
HCMCPFGN_02256 | 3.8e-50 | |||||
HCMCPFGN_02257 | 6.1e-213 | ywhK | S | Membrane | ||
HCMCPFGN_02258 | 2.4e-23 | ykuL | S | IMP dehydrogenase activity | ||
HCMCPFGN_02259 | 4.6e-203 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02260 | 0.0 | cadA | P | P-type ATPase | ||
HCMCPFGN_02261 | 1.2e-203 | napA | P | Sodium/hydrogen exchanger family | ||
HCMCPFGN_02262 | 1.5e-49 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
HCMCPFGN_02263 | 3.6e-47 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
HCMCPFGN_02264 | 4.4e-262 | V | ABC transporter transmembrane region | |||
HCMCPFGN_02265 | 5.1e-76 | S | Putative adhesin | |||
HCMCPFGN_02266 | 1.5e-155 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
HCMCPFGN_02267 | 1.6e-45 | |||||
HCMCPFGN_02268 | 4.4e-217 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02269 | 2.1e-117 | S | CAAX protease self-immunity | |||
HCMCPFGN_02270 | 1.9e-195 | S | DUF218 domain | |||
HCMCPFGN_02271 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
HCMCPFGN_02272 | 5.5e-96 | S | ECF transporter, substrate-specific component | |||
HCMCPFGN_02273 | 2.2e-159 | yeaE | S | Aldo/keto reductase family | ||
HCMCPFGN_02274 | 3.9e-133 | 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 | |
HCMCPFGN_02275 | 6.1e-101 | ybbH_2 | K | rpiR family | ||
HCMCPFGN_02276 | 8.5e-145 | S | Bacterial protein of unknown function (DUF871) | |||
HCMCPFGN_02277 | 4.3e-190 | yfeW | 3.4.16.4 | V | Beta-lactamase | |
HCMCPFGN_02278 | 4.3e-121 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
HCMCPFGN_02279 | 0.0 | sacX | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
HCMCPFGN_02281 | 2.7e-117 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HCMCPFGN_02282 | 1.8e-127 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
HCMCPFGN_02283 | 2.7e-213 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
HCMCPFGN_02284 | 1.1e-144 | cof | S | haloacid dehalogenase-like hydrolase | ||
HCMCPFGN_02285 | 4.8e-230 | pbuG | S | permease | ||
HCMCPFGN_02286 | 2.2e-174 | S | cog cog1373 | |||
HCMCPFGN_02287 | 3.5e-219 | L | transposase, IS605 OrfB family | |||
HCMCPFGN_02288 | 3.2e-10 | S | cog cog1373 | |||
HCMCPFGN_02289 | 4.7e-85 | K | helix_turn_helix, mercury resistance | |||
HCMCPFGN_02290 | 7.5e-25 | K | helix_turn_helix, mercury resistance | |||
HCMCPFGN_02291 | 8.2e-230 | pbuG | S | permease | ||
HCMCPFGN_02292 | 9.1e-243 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_02293 | 6.7e-224 | pbuG | S | permease | ||
HCMCPFGN_02294 | 2.3e-35 | |||||
HCMCPFGN_02295 | 2.7e-76 | atkY | K | Penicillinase repressor | ||
HCMCPFGN_02296 | 1.2e-64 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HCMCPFGN_02297 | 1.4e-49 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
HCMCPFGN_02298 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
HCMCPFGN_02299 | 5.6e-17 | EGP | Sugar (and other) transporter | |||
HCMCPFGN_02300 | 2.2e-38 | EGP | Sugar (and other) transporter | |||
HCMCPFGN_02301 | 8.5e-81 | EGP | Sugar (and other) transporter | |||
HCMCPFGN_02302 | 1.2e-18 | |||||
HCMCPFGN_02303 | 6.1e-210 | |||||
HCMCPFGN_02304 | 3.2e-281 | clcA | P | chloride | ||
HCMCPFGN_02305 | 1.1e-269 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
HCMCPFGN_02306 | 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 | ||
HCMCPFGN_02307 | 6.2e-252 | 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 | ||
HCMCPFGN_02308 | 3e-143 | 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 | ||
HCMCPFGN_02309 | 2.7e-61 | 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 | |
HCMCPFGN_02310 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
HCMCPFGN_02311 | 2.3e-262 | S | Uncharacterised protein family (UPF0236) | |||
HCMCPFGN_02312 | 1.8e-13 | ytgB | S | Transglycosylase associated protein | ||
HCMCPFGN_02313 | 7.7e-103 | tnpR | L | Resolvase, N terminal domain | ||
HCMCPFGN_02314 | 2.7e-160 | |||||
HCMCPFGN_02315 | 6.9e-248 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
HCMCPFGN_02316 | 9.9e-52 | |||||
HCMCPFGN_02317 | 7.2e-65 | |||||
HCMCPFGN_02318 | 8.3e-171 | hprA | 1.1.1.29 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HCMCPFGN_02319 | 1.8e-196 | L | Psort location Cytoplasmic, score | |||
HCMCPFGN_02320 | 2e-32 | |||||
HCMCPFGN_02321 | 2.1e-237 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
HCMCPFGN_02322 | 0.0 | traA | L | MobA MobL family protein | ||
HCMCPFGN_02323 | 1.7e-23 | |||||
HCMCPFGN_02324 | 5.2e-41 | |||||
HCMCPFGN_02325 | 2e-124 | S | Fic/DOC family | |||
HCMCPFGN_02326 | 1.9e-155 | repA | S | Replication initiator protein A | ||
HCMCPFGN_02327 | 7.2e-43 | |||||
HCMCPFGN_02328 | 3.1e-195 | O | Heat shock 70 kDa protein | |||
HCMCPFGN_02329 | 3.6e-112 | EGP | Major facilitator Superfamily | |||
HCMCPFGN_02330 | 5e-62 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
HCMCPFGN_02332 | 1.9e-98 | F | DNA/RNA non-specific endonuclease | |||
HCMCPFGN_02333 | 1.9e-75 | S | BstXI restriction endonuclease | |||
HCMCPFGN_02334 | 8e-11 | K | Helix-turn-helix XRE-family like proteins | |||
HCMCPFGN_02335 | 2.1e-100 | 2.1.1.72 | L | DNA methylase | ||
HCMCPFGN_02337 | 3e-41 | repA | S | Replication initiator protein A |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)