ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
BCJHNJMD_00001 | 2.1e-29 | 3.4.22.70 | M | by MetaGeneAnnotator | ||
BCJHNJMD_00006 | 3.2e-139 | clpB | O | Belongs to the ClpA ClpB family | ||
BCJHNJMD_00008 | 1.3e-94 | topB | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
BCJHNJMD_00009 | 1.4e-21 | L | Psort location Cytoplasmic, score | |||
BCJHNJMD_00010 | 6.1e-43 | S | PFAM Uncharacterised protein family UPF0150 | |||
BCJHNJMD_00011 | 2e-17 | N | PFAM YcfA family protein | |||
BCJHNJMD_00012 | 3.8e-21 | |||||
BCJHNJMD_00013 | 1.6e-20 | |||||
BCJHNJMD_00014 | 7.5e-183 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
BCJHNJMD_00015 | 3.2e-24 | L | Protein of unknown function (DUF3991) | |||
BCJHNJMD_00017 | 2e-25 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
BCJHNJMD_00022 | 2.4e-08 | CO | Thioredoxin | |||
BCJHNJMD_00025 | 1.2e-36 | S | Protein of unknown function (DUF3102) | |||
BCJHNJMD_00026 | 3.4e-110 | K | Primase C terminal 1 (PriCT-1) | |||
BCJHNJMD_00027 | 1.3e-41 | soj | D | Sporulation initiation inhibitor | ||
BCJHNJMD_00031 | 4.7e-28 | M | CHAP domain | |||
BCJHNJMD_00032 | 3e-127 | U | type IV secretory pathway VirB4 | |||
BCJHNJMD_00033 | 3.7e-21 | |||||
BCJHNJMD_00035 | 5e-26 | I | mechanosensitive ion channel activity | |||
BCJHNJMD_00036 | 5.5e-127 | U | TraM recognition site of TraD and TraG | |||
BCJHNJMD_00037 | 2.2e-30 | tnp | L | DDE domain | ||
BCJHNJMD_00039 | 1.1e-92 | L | PFAM Integrase catalytic region | |||
BCJHNJMD_00040 | 4.2e-30 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
BCJHNJMD_00043 | 7e-87 | L | Belongs to the 'phage' integrase family | |||
BCJHNJMD_00044 | 1.1e-305 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
BCJHNJMD_00045 | 2.3e-99 | aacA4_1 | 4.1.1.17 | K | acetyltransferase | |
BCJHNJMD_00046 | 7e-175 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
BCJHNJMD_00047 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
BCJHNJMD_00048 | 2.6e-290 | yjbQ | P | TrkA C-terminal domain protein | ||
BCJHNJMD_00049 | 8.5e-119 | G | phosphoglycerate mutase | |||
BCJHNJMD_00050 | 1.3e-179 | oppF | P | Belongs to the ABC transporter superfamily | ||
BCJHNJMD_00051 | 4.5e-205 | oppD | P | Belongs to the ABC transporter superfamily | ||
BCJHNJMD_00052 | 2.6e-186 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BCJHNJMD_00053 | 2.2e-152 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
BCJHNJMD_00054 | 2.8e-304 | oppA | E | ABC transporter, substratebinding protein | ||
BCJHNJMD_00055 | 6.7e-306 | oppA | E | ABC transporter, substratebinding protein | ||
BCJHNJMD_00056 | 3.5e-225 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
BCJHNJMD_00057 | 1.6e-109 | glnP | P | ABC transporter permease | ||
BCJHNJMD_00058 | 1.1e-110 | gluC | P | ABC transporter permease | ||
BCJHNJMD_00059 | 1.2e-149 | glnH | ET | ABC transporter substrate-binding protein | ||
BCJHNJMD_00060 | 1.6e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BCJHNJMD_00061 | 1.8e-170 | |||||
BCJHNJMD_00062 | 5.3e-13 | 3.2.1.14 | GH18 | |||
BCJHNJMD_00063 | 1.4e-78 | zur | P | Belongs to the Fur family | ||
BCJHNJMD_00064 | 2.3e-75 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
BCJHNJMD_00065 | 4.4e-76 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
BCJHNJMD_00066 | 1.2e-242 | yfnA | E | Amino Acid | ||
BCJHNJMD_00067 | 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 | |
BCJHNJMD_00068 | 1.1e-177 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
BCJHNJMD_00069 | 4.6e-87 | M | ErfK YbiS YcfS YnhG | |||
BCJHNJMD_00070 | 6.7e-295 | S | ABC transporter, ATP-binding protein | |||
BCJHNJMD_00071 | 4e-68 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
BCJHNJMD_00072 | 1.5e-126 | XK27_07075 | S | CAAX protease self-immunity | ||
BCJHNJMD_00073 | 2.2e-120 | cmpC | S | ATPases associated with a variety of cellular activities | ||
BCJHNJMD_00074 | 7.3e-167 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
BCJHNJMD_00075 | 9.5e-167 | XK27_00670 | S | ABC transporter | ||
BCJHNJMD_00076 | 1.1e-161 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
BCJHNJMD_00077 | 2.9e-179 | XK27_08835 | S | ABC transporter | ||
BCJHNJMD_00078 | 3.9e-154 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
BCJHNJMD_00079 | 3.3e-138 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00080 | 9.7e-52 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_00081 | 2.7e-54 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_00082 | 3.5e-114 | S | Fn3-like domain | |||
BCJHNJMD_00084 | 2.4e-219 | |||||
BCJHNJMD_00086 | 9.5e-158 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
BCJHNJMD_00087 | 5.2e-128 | terC | P | integral membrane protein, YkoY family | ||
BCJHNJMD_00088 | 1.7e-243 | pbpX1 | V | SH3-like domain | ||
BCJHNJMD_00089 | 6.9e-110 | NU | mannosyl-glycoprotein | |||
BCJHNJMD_00090 | 3.1e-181 | S | DUF218 domain | |||
BCJHNJMD_00091 | 8.1e-190 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
BCJHNJMD_00092 | 4.5e-135 | IQ | reductase | |||
BCJHNJMD_00093 | 1.1e-15 | |||||
BCJHNJMD_00094 | 0.0 | ydgH | S | MMPL family | ||
BCJHNJMD_00095 | 3.9e-257 | ydiC1 | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00096 | 1.6e-91 | K | Transcriptional regulator PadR-like family | |||
BCJHNJMD_00097 | 6e-82 | merR | K | MerR family regulatory protein | ||
BCJHNJMD_00098 | 2.6e-61 | iap | CBM50 | M | NlpC P60 family | |
BCJHNJMD_00099 | 8.3e-78 | yjcF | K | protein acetylation | ||
BCJHNJMD_00100 | 9.9e-123 | pgm3 | G | phosphoglycerate mutase family | ||
BCJHNJMD_00101 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BCJHNJMD_00102 | 2e-180 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
BCJHNJMD_00103 | 9.9e-143 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BCJHNJMD_00104 | 1e-190 | S | Protease prsW family | |||
BCJHNJMD_00105 | 7e-178 | iunH2 | 3.2.2.1, 3.2.2.8 | F | nucleoside hydrolase | |
BCJHNJMD_00106 | 1.6e-07 | yvlA | ||||
BCJHNJMD_00107 | 1.4e-73 | |||||
BCJHNJMD_00108 | 3.4e-149 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
BCJHNJMD_00109 | 1.1e-115 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BCJHNJMD_00110 | 6.9e-17 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BCJHNJMD_00111 | 4.1e-234 | 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 | |||
BCJHNJMD_00112 | 5.8e-72 | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
BCJHNJMD_00113 | 2.5e-138 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
BCJHNJMD_00114 | 4e-56 | S | LuxR family transcriptional regulator | |||
BCJHNJMD_00115 | 6.7e-127 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
BCJHNJMD_00116 | 5e-218 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BCJHNJMD_00117 | 3.4e-169 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BCJHNJMD_00118 | 4.4e-95 | S | ABC transporter permease | |||
BCJHNJMD_00119 | 1.9e-256 | P | ABC transporter | |||
BCJHNJMD_00120 | 7.5e-115 | P | Cobalt transport protein | |||
BCJHNJMD_00121 | 1.3e-119 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
BCJHNJMD_00122 | 6.6e-60 | |||||
BCJHNJMD_00123 | 1.1e-08 | |||||
BCJHNJMD_00125 | 5.5e-32 | |||||
BCJHNJMD_00126 | 7.1e-217 | |||||
BCJHNJMD_00127 | 3e-187 | ansA | 3.5.1.1 | EJ | Asparaginase | |
BCJHNJMD_00128 | 2.9e-25 | |||||
BCJHNJMD_00129 | 5.5e-248 | pbuX | F | xanthine permease | ||
BCJHNJMD_00130 | 7.2e-169 | natA | S | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00131 | 4.7e-211 | natB | CP | ABC-2 family transporter protein | ||
BCJHNJMD_00133 | 1.8e-251 | yjjP | S | Putative threonine/serine exporter | ||
BCJHNJMD_00134 | 1.9e-153 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
BCJHNJMD_00135 | 2.9e-153 | 1.1.1.2, 1.1.1.307 | C | Aldo keto reductase | ||
BCJHNJMD_00136 | 3.4e-64 | S | Protein of unknown function (DUF1722) | |||
BCJHNJMD_00137 | 3.8e-68 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
BCJHNJMD_00138 | 1.4e-280 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
BCJHNJMD_00139 | 1.7e-125 | K | Crp-like helix-turn-helix domain | |||
BCJHNJMD_00140 | 8e-238 | larA | 5.1.2.1 | S | Domain of unknown function (DUF2088) | |
BCJHNJMD_00141 | 7.9e-132 | cpmA | S | AIR carboxylase | ||
BCJHNJMD_00142 | 1.2e-227 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
BCJHNJMD_00143 | 1.6e-149 | larE | S | NAD synthase | ||
BCJHNJMD_00144 | 1.7e-122 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
BCJHNJMD_00145 | 1.4e-178 | hoxN | U | High-affinity nickel-transport protein | ||
BCJHNJMD_00146 | 2e-103 | aroD | S | Serine hydrolase (FSH1) | ||
BCJHNJMD_00147 | 5.4e-42 | GnaT | 2.5.1.16 | K | Acetyltransferase (GNAT) domain | |
BCJHNJMD_00148 | 5.9e-24 | |||||
BCJHNJMD_00149 | 1.6e-18 | S | Bacteriocin helveticin-J | |||
BCJHNJMD_00150 | 3.1e-209 | 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 | |
BCJHNJMD_00151 | 3.8e-148 | potB | P | ABC transporter permease | ||
BCJHNJMD_00152 | 6.8e-134 | potC | P | ABC transporter permease | ||
BCJHNJMD_00153 | 3.4e-205 | potD | P | ABC transporter | ||
BCJHNJMD_00154 | 8.3e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
BCJHNJMD_00155 | 3e-143 | pstA | P | Phosphate transport system permease protein PstA | ||
BCJHNJMD_00156 | 1e-168 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
BCJHNJMD_00157 | 2.4e-156 | pstS | P | Phosphate | ||
BCJHNJMD_00158 | 1.7e-57 | |||||
BCJHNJMD_00159 | 2.7e-31 | |||||
BCJHNJMD_00160 | 1.8e-43 | |||||
BCJHNJMD_00161 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
BCJHNJMD_00162 | 1.2e-123 | |||||
BCJHNJMD_00163 | 2e-174 | sepS16B | ||||
BCJHNJMD_00164 | 2.5e-197 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
BCJHNJMD_00165 | 5.9e-79 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
BCJHNJMD_00166 | 1.8e-295 | E | amino acid | |||
BCJHNJMD_00167 | 1.1e-116 | S | membrane | |||
BCJHNJMD_00168 | 3.7e-112 | S | VIT family | |||
BCJHNJMD_00169 | 5.7e-91 | perR | P | Belongs to the Fur family | ||
BCJHNJMD_00170 | 7.1e-179 | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase | |
BCJHNJMD_00172 | 1e-126 | yibF | S | overlaps another CDS with the same product name | ||
BCJHNJMD_00173 | 2.2e-199 | yibE | S | overlaps another CDS with the same product name | ||
BCJHNJMD_00175 | 2.8e-82 | uspA | T | Belongs to the universal stress protein A family | ||
BCJHNJMD_00176 | 2.7e-131 | |||||
BCJHNJMD_00177 | 7.5e-18 | S | CAAX protease self-immunity | |||
BCJHNJMD_00178 | 7.4e-86 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BCJHNJMD_00179 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
BCJHNJMD_00180 | 9.5e-92 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
BCJHNJMD_00181 | 2.2e-20 | |||||
BCJHNJMD_00183 | 3.6e-32 | V | AAA domain, putative AbiEii toxin, Type IV TA system | |||
BCJHNJMD_00185 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
BCJHNJMD_00187 | 3.7e-185 | galR | K | Transcriptional regulator | ||
BCJHNJMD_00188 | 2.2e-284 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
BCJHNJMD_00189 | 3.1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
BCJHNJMD_00190 | 7.4e-222 | 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) | |
BCJHNJMD_00191 | 1.1e-211 | gph | G | Transporter | ||
BCJHNJMD_00192 | 2.6e-36 | |||||
BCJHNJMD_00193 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
BCJHNJMD_00194 | 2.7e-196 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
BCJHNJMD_00195 | 2.2e-207 | mmgC | 1.3.8.1 | I | Acyl-CoA dehydrogenase, C-terminal domain | |
BCJHNJMD_00196 | 3.2e-144 | etfB | C | Electron transfer flavoprotein domain | ||
BCJHNJMD_00197 | 6.6e-176 | etfA | C | Electron transfer flavoprotein FAD-binding domain | ||
BCJHNJMD_00198 | 6.2e-185 | 1.1.1.1 | C | nadph quinone reductase | ||
BCJHNJMD_00199 | 3.2e-53 | K | Transcriptional | |||
BCJHNJMD_00200 | 5.4e-124 | hchA | 3.5.1.124 | S | DJ-1/PfpI family | |
BCJHNJMD_00201 | 0.0 | oppD | EP | Psort location Cytoplasmic, score | ||
BCJHNJMD_00202 | 1.9e-76 | K | Transcriptional regulator, LysR family | |||
BCJHNJMD_00203 | 8.9e-186 | oxlT | G | Major Facilitator Superfamily | ||
BCJHNJMD_00204 | 1.5e-126 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
BCJHNJMD_00205 | 8.5e-132 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BCJHNJMD_00206 | 1.1e-80 | 6.3.3.2 | S | ASCH | ||
BCJHNJMD_00207 | 7.5e-245 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00208 | 2.3e-23 | |||||
BCJHNJMD_00209 | 1.9e-152 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
BCJHNJMD_00210 | 4.8e-139 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
BCJHNJMD_00211 | 3.2e-158 | hipB | K | Helix-turn-helix | ||
BCJHNJMD_00212 | 1.8e-118 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
BCJHNJMD_00213 | 7.5e-70 | yeaO | S | Protein of unknown function, DUF488 | ||
BCJHNJMD_00214 | 3e-122 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | HAD-hyrolase-like |
BCJHNJMD_00215 | 2.3e-78 | usp1 | T | Universal stress protein family | ||
BCJHNJMD_00216 | 6.2e-264 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
BCJHNJMD_00217 | 9.1e-115 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
BCJHNJMD_00218 | 1e-81 | S | 3-demethylubiquinone-9 3-methyltransferase | |||
BCJHNJMD_00219 | 2.7e-143 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BCJHNJMD_00220 | 4.5e-85 | |||||
BCJHNJMD_00221 | 1.8e-239 | codA | 3.5.4.1 | F | cytosine deaminase | |
BCJHNJMD_00222 | 1.4e-47 | |||||
BCJHNJMD_00223 | 3.3e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BCJHNJMD_00224 | 5.2e-18 | |||||
BCJHNJMD_00225 | 1.2e-123 | yrkL | S | Flavodoxin-like fold | ||
BCJHNJMD_00227 | 6.2e-30 | |||||
BCJHNJMD_00229 | 5.1e-37 | S | Cytochrome B5 | |||
BCJHNJMD_00230 | 2.1e-31 | cspC | K | Cold shock protein | ||
BCJHNJMD_00231 | 1.7e-108 | XK27_00220 | S | Dienelactone hydrolase family | ||
BCJHNJMD_00232 | 4.4e-52 | |||||
BCJHNJMD_00233 | 8.8e-220 | mutY | L | A G-specific adenine glycosylase | ||
BCJHNJMD_00234 | 5.4e-303 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
BCJHNJMD_00235 | 0.0 | pelX | M | domain, Protein | ||
BCJHNJMD_00236 | 4.8e-51 | |||||
BCJHNJMD_00237 | 5.1e-190 | 6.3.1.20 | H | Lipoate-protein ligase | ||
BCJHNJMD_00238 | 6.3e-66 | gcvH | E | glycine cleavage | ||
BCJHNJMD_00239 | 3.3e-183 | tas | C | Aldo/keto reductase family | ||
BCJHNJMD_00240 | 2.1e-32 | |||||
BCJHNJMD_00241 | 1.6e-177 | EG | EamA-like transporter family | |||
BCJHNJMD_00242 | 1.1e-113 | metI | P | ABC transporter permease | ||
BCJHNJMD_00243 | 6.5e-193 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
BCJHNJMD_00244 | 1e-145 | P | Belongs to the nlpA lipoprotein family | |||
BCJHNJMD_00245 | 5.9e-97 | tag | 3.2.2.20 | L | glycosylase | |
BCJHNJMD_00246 | 0.0 | E | ABC transporter, substratebinding protein | |||
BCJHNJMD_00248 | 0.0 | 3.2.1.21 | GH3 | G | hydrolase, family 3 | |
BCJHNJMD_00249 | 1.1e-189 | pva1 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
BCJHNJMD_00250 | 9.3e-304 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
BCJHNJMD_00251 | 4.5e-208 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
BCJHNJMD_00252 | 6.7e-104 | tag | 3.2.2.20 | L | glycosylase | |
BCJHNJMD_00253 | 8.9e-146 | S | Zinc-dependent metalloprotease | |||
BCJHNJMD_00254 | 2.9e-168 | XK27_00880 | 3.5.1.28 | M | hydrolase, family 25 | |
BCJHNJMD_00255 | 1.5e-203 | G | Glycosyl hydrolases family 8 | |||
BCJHNJMD_00256 | 7.3e-55 | yphJ | 4.1.1.44 | S | decarboxylase | |
BCJHNJMD_00257 | 1.6e-78 | yphH | S | Cupin domain | ||
BCJHNJMD_00258 | 2.9e-75 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_00259 | 4.5e-100 | yobS | K | Bacterial regulatory proteins, tetR family | ||
BCJHNJMD_00260 | 6.9e-10 | K | MarR family | |||
BCJHNJMD_00261 | 7.8e-230 | |||||
BCJHNJMD_00262 | 6e-157 | dkgB | S | reductase | ||
BCJHNJMD_00263 | 2.1e-200 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00264 | 3e-194 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00265 | 2.8e-134 | C | Oxidoreductase | |||
BCJHNJMD_00266 | 1.9e-40 | ccmL | CQ | Ethanolamine utilisation protein EutN/carboxysome | ||
BCJHNJMD_00267 | 3.7e-59 | K | helix_turn_helix, arabinose operon control protein | |||
BCJHNJMD_00268 | 7.5e-60 | S | Domain of unknown function (DUF4430) | |||
BCJHNJMD_00269 | 3.8e-177 | U | FFAT motif binding | |||
BCJHNJMD_00270 | 4e-113 | S | ECF-type riboflavin transporter, S component | |||
BCJHNJMD_00271 | 4e-306 | ykoD_2 | S | AAA domain, putative AbiEii toxin, Type IV TA system | ||
BCJHNJMD_00272 | 5.2e-159 | P | ABC-type cobalt transport system permease component CbiQ and related transporters | |||
BCJHNJMD_00273 | 1.8e-69 | |||||
BCJHNJMD_00274 | 2.1e-97 | 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 | |
BCJHNJMD_00275 | 1.1e-283 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
BCJHNJMD_00276 | 6.1e-160 | K | LysR substrate binding domain | |||
BCJHNJMD_00277 | 4.6e-70 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
BCJHNJMD_00278 | 0.0 | epsA | I | PAP2 superfamily | ||
BCJHNJMD_00279 | 6e-55 | S | Domain of unknown function (DU1801) | |||
BCJHNJMD_00280 | 3.2e-110 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
BCJHNJMD_00281 | 1.4e-107 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
BCJHNJMD_00282 | 0.0 | lmrA | 3.6.3.44 | V | ABC transporter | |
BCJHNJMD_00283 | 3.3e-92 | rmaB | K | Transcriptional regulator, MarR family | ||
BCJHNJMD_00284 | 6.3e-123 | S | membrane transporter protein | |||
BCJHNJMD_00285 | 5.2e-139 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
BCJHNJMD_00286 | 2.4e-120 | |||||
BCJHNJMD_00287 | 2.1e-123 | skfE | V | ATPases associated with a variety of cellular activities | ||
BCJHNJMD_00288 | 1.9e-62 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
BCJHNJMD_00289 | 2.3e-173 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
BCJHNJMD_00290 | 6.9e-86 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
BCJHNJMD_00291 | 6.8e-128 | S | haloacid dehalogenase-like hydrolase | |||
BCJHNJMD_00292 | 2.2e-202 | bcr1 | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00293 | 6.6e-145 | S | Sucrose-6F-phosphate phosphohydrolase | |||
BCJHNJMD_00294 | 4.7e-156 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
BCJHNJMD_00295 | 3.3e-100 | |||||
BCJHNJMD_00296 | 2.2e-131 | ydfG | S | KR domain | ||
BCJHNJMD_00297 | 3e-65 | hxlR | K | HxlR-like helix-turn-helix | ||
BCJHNJMD_00298 | 7.4e-60 | asp2 | S | Asp23 family, cell envelope-related function | ||
BCJHNJMD_00299 | 3.6e-70 | asp | S | Asp23 family, cell envelope-related function | ||
BCJHNJMD_00300 | 5.9e-25 | |||||
BCJHNJMD_00301 | 1.1e-90 | |||||
BCJHNJMD_00302 | 4.4e-18 | S | Transglycosylase associated protein | |||
BCJHNJMD_00303 | 2.1e-155 | |||||
BCJHNJMD_00304 | 1.9e-270 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
BCJHNJMD_00305 | 6.8e-183 | chaT1 | U | Major Facilitator Superfamily | ||
BCJHNJMD_00306 | 6.3e-94 | laaE | K | Transcriptional regulator PadR-like family | ||
BCJHNJMD_00307 | 1e-66 | lysM | M | LysM domain | ||
BCJHNJMD_00308 | 8.2e-131 | XK27_07210 | 6.1.1.6 | S | B3 4 domain | |
BCJHNJMD_00309 | 6.6e-122 | iprA | K | Cyclic nucleotide-monophosphate binding domain | ||
BCJHNJMD_00310 | 6.2e-171 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
BCJHNJMD_00311 | 6.8e-217 | arcT | 2.6.1.1 | E | Aminotransferase | |
BCJHNJMD_00312 | 5e-257 | arcD | E | Arginine ornithine antiporter | ||
BCJHNJMD_00313 | 3.3e-197 | argF | 2.1.3.3, 2.1.3.6, 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 | |
BCJHNJMD_00314 | 7.7e-238 | arcA | 3.5.3.6 | E | Arginine | |
BCJHNJMD_00315 | 5.7e-278 | S | C4-dicarboxylate anaerobic carrier | |||
BCJHNJMD_00316 | 9.1e-221 | 2.1.1.80, 2.7.13.3, 3.1.1.61 | T | histidine kinase DNA gyrase B | ||
BCJHNJMD_00317 | 6.5e-148 | KT | YcbB domain | |||
BCJHNJMD_00318 | 1.2e-280 | arcD | S | C4-dicarboxylate anaerobic carrier | ||
BCJHNJMD_00319 | 1.1e-258 | ytjP | 3.5.1.18 | E | Dipeptidase | |
BCJHNJMD_00321 | 2.5e-209 | ykiI | ||||
BCJHNJMD_00322 | 1.1e-104 | thiJ-2 | 3.5.1.124 | S | DJ-1/PfpI family | |
BCJHNJMD_00323 | 1.4e-191 | yjcE | P | Sodium proton antiporter | ||
BCJHNJMD_00324 | 3.2e-159 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
BCJHNJMD_00325 | 1.6e-59 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | S | MucBP domain | |
BCJHNJMD_00326 | 1.5e-221 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00327 | 2e-68 | yobT | S | PFAM Metallo-beta-lactamase superfamily | ||
BCJHNJMD_00328 | 4.8e-16 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_00330 | 5.2e-35 | S | Protein of unknown function (DUF3781) | |||
BCJHNJMD_00331 | 1.7e-38 | |||||
BCJHNJMD_00332 | 4.3e-80 | yafP | 3.6.4.13 | K | Acetyltransferase (GNAT) domain | |
BCJHNJMD_00333 | 3.6e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
BCJHNJMD_00334 | 1.9e-262 | M | domain protein | |||
BCJHNJMD_00335 | 1.8e-169 | K | AI-2E family transporter | |||
BCJHNJMD_00336 | 3.7e-210 | xylR | GK | ROK family | ||
BCJHNJMD_00337 | 3e-122 | |||||
BCJHNJMD_00338 | 3.7e-237 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
BCJHNJMD_00339 | 1.3e-52 | azlD | S | branched-chain amino acid | ||
BCJHNJMD_00340 | 7.2e-136 | azlC | E | AzlC protein | ||
BCJHNJMD_00341 | 3.3e-86 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
BCJHNJMD_00342 | 1.6e-249 | gor | 1.8.1.7 | C | Glutathione reductase | |
BCJHNJMD_00343 | 2.8e-36 | S | Domain of unknown function (DUF4430) | |||
BCJHNJMD_00344 | 2.8e-175 | V | domain protein | |||
BCJHNJMD_00345 | 1.7e-238 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BCJHNJMD_00346 | 7.4e-214 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
BCJHNJMD_00347 | 3.5e-123 | K | response regulator | |||
BCJHNJMD_00348 | 2.8e-210 | 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 | |
BCJHNJMD_00349 | 1e-107 | |||||
BCJHNJMD_00350 | 3.1e-133 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
BCJHNJMD_00351 | 4.4e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
BCJHNJMD_00352 | 8.5e-33 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
BCJHNJMD_00353 | 3.4e-155 | spo0J | K | Belongs to the ParB family | ||
BCJHNJMD_00354 | 4.1e-136 | soj | D | Sporulation initiation inhibitor | ||
BCJHNJMD_00355 | 1.2e-146 | noc | K | Belongs to the ParB family | ||
BCJHNJMD_00356 | 6.4e-131 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
BCJHNJMD_00357 | 1.8e-164 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
BCJHNJMD_00358 | 2.8e-168 | rihC | 3.2.2.1, 3.2.2.8 | F | Nucleoside | |
BCJHNJMD_00359 | 1.3e-214 | pbuO_1 | S | Permease family | ||
BCJHNJMD_00360 | 5.3e-226 | nupG | F | Nucleoside | ||
BCJHNJMD_00361 | 2.3e-153 | 5.4.2.7 | G | Metalloenzyme superfamily | ||
BCJHNJMD_00362 | 4e-113 | GM | NmrA-like family | |||
BCJHNJMD_00363 | 6.3e-44 | |||||
BCJHNJMD_00364 | 1.1e-85 | |||||
BCJHNJMD_00365 | 1.6e-39 | |||||
BCJHNJMD_00366 | 1.1e-62 | K | HxlR-like helix-turn-helix | |||
BCJHNJMD_00367 | 5.5e-35 | |||||
BCJHNJMD_00368 | 8.2e-106 | |||||
BCJHNJMD_00369 | 7.3e-136 | |||||
BCJHNJMD_00371 | 1.6e-276 | |||||
BCJHNJMD_00372 | 4.5e-72 | |||||
BCJHNJMD_00373 | 2.1e-66 | |||||
BCJHNJMD_00374 | 1.3e-221 | EK | Aminotransferase, class I | |||
BCJHNJMD_00375 | 4.9e-165 | K | LysR substrate binding domain | |||
BCJHNJMD_00376 | 4.8e-11 | S | Protein of unknown function (DUF2922) | |||
BCJHNJMD_00377 | 2.3e-27 | |||||
BCJHNJMD_00378 | 9.9e-100 | K | DNA-templated transcription, initiation | |||
BCJHNJMD_00379 | 3.7e-207 | |||||
BCJHNJMD_00380 | 7.6e-59 | |||||
BCJHNJMD_00381 | 2.6e-52 | |||||
BCJHNJMD_00382 | 1.6e-196 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
BCJHNJMD_00384 | 1.4e-286 | macB3 | V | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00385 | 2.1e-109 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
BCJHNJMD_00386 | 7.8e-146 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
BCJHNJMD_00387 | 1.8e-139 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
BCJHNJMD_00388 | 7e-150 | vdlC | S | Enoyl-(Acyl carrier protein) reductase | ||
BCJHNJMD_00389 | 1.4e-128 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
BCJHNJMD_00390 | 2.7e-117 | ybbL | S | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00391 | 9.4e-275 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BCJHNJMD_00392 | 2.6e-91 | |||||
BCJHNJMD_00396 | 1.2e-133 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
BCJHNJMD_00397 | 4.9e-131 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_00398 | 1.5e-222 | xylR | GK | ROK family | ||
BCJHNJMD_00399 | 2.9e-159 | akr5f | 1.1.1.346 | C | Aldo keto reductase | |
BCJHNJMD_00400 | 5.2e-248 | rarA | L | recombination factor protein RarA | ||
BCJHNJMD_00401 | 1.8e-279 | rny | S | Endoribonuclease that initiates mRNA decay | ||
BCJHNJMD_00402 | 7e-127 | yoaK | S | Protein of unknown function (DUF1275) | ||
BCJHNJMD_00403 | 4.2e-175 | D | Alpha beta | |||
BCJHNJMD_00404 | 0.0 | pepF2 | E | Oligopeptidase F | ||
BCJHNJMD_00405 | 1.2e-73 | K | Transcriptional regulator | |||
BCJHNJMD_00406 | 1.9e-163 | |||||
BCJHNJMD_00407 | 1.1e-187 | S | DUF218 domain | |||
BCJHNJMD_00408 | 4.3e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
BCJHNJMD_00409 | 1.1e-156 | nanK | 2.7.1.2 | GK | ROK family | |
BCJHNJMD_00410 | 2.1e-244 | frlA | E | Amino acid permease | ||
BCJHNJMD_00411 | 1.9e-25 | |||||
BCJHNJMD_00412 | 2e-27 | |||||
BCJHNJMD_00414 | 3.6e-177 | S | DNA/RNA non-specific endonuclease | |||
BCJHNJMD_00415 | 7.4e-63 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
BCJHNJMD_00416 | 5.7e-19 | K | Acetyltransferase (GNAT) family | |||
BCJHNJMD_00417 | 3e-177 | dcuD | C | Tripartite ATP-independent periplasmic transporter, DctM component | ||
BCJHNJMD_00418 | 8.2e-115 | rihB | 3.2.2.1 | F | Nucleoside | |
BCJHNJMD_00420 | 2.7e-49 | |||||
BCJHNJMD_00421 | 1.1e-77 | K | Winged helix DNA-binding domain | |||
BCJHNJMD_00422 | 1.7e-111 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the epimerization of the S- and R-forms of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration. This is a prerequisite for the S- specific NAD(P)H-hydrate dehydratase to allow the repair of both epimers of NAD(P)HX | |
BCJHNJMD_00423 | 7.2e-32 | arsR | K | DNA-binding transcription factor activity | ||
BCJHNJMD_00424 | 4.1e-204 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00425 | 1.3e-102 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
BCJHNJMD_00426 | 7.9e-114 | |||||
BCJHNJMD_00427 | 7.2e-183 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
BCJHNJMD_00428 | 3.8e-84 | iap | CBM50 | M | NlpC P60 family | |
BCJHNJMD_00429 | 6.4e-293 | ytgP | S | Polysaccharide biosynthesis protein | ||
BCJHNJMD_00430 | 7.2e-59 | K | Helix-turn-helix domain | |||
BCJHNJMD_00431 | 0.0 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
BCJHNJMD_00432 | 9.1e-167 | panE2 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
BCJHNJMD_00433 | 3.3e-43 | |||||
BCJHNJMD_00434 | 1.9e-65 | 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 | |
BCJHNJMD_00435 | 0.0 | yjcE | P | Sodium proton antiporter | ||
BCJHNJMD_00436 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
BCJHNJMD_00437 | 1.3e-304 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
BCJHNJMD_00438 | 5.2e-119 | yoaK | S | Protein of unknown function (DUF1275) | ||
BCJHNJMD_00439 | 1.5e-156 | rihA | F | Inosine-uridine preferring nucleoside hydrolase | ||
BCJHNJMD_00441 | 3.2e-188 | nupC | F | Na+ dependent nucleoside transporter C-terminus | ||
BCJHNJMD_00442 | 2.2e-149 | 1.1.1.1 | C | alcohol dehydrogenase | ||
BCJHNJMD_00443 | 3.3e-75 | S | Membrane | |||
BCJHNJMD_00444 | 3.7e-112 | trpF | 5.3.1.24 | E | belongs to the TrpF family | |
BCJHNJMD_00445 | 1.4e-122 | yeiI | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | Phosphomethylpyrimidine kinase | |
BCJHNJMD_00446 | 2.1e-109 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | GK | Winged helix-turn-helix DNA-binding | |
BCJHNJMD_00448 | 1.9e-178 | K | helix_turn _helix lactose operon repressor | |||
BCJHNJMD_00449 | 1.7e-26 | mcbG | S | Pentapeptide repeats (8 copies) | ||
BCJHNJMD_00450 | 1e-99 | ywlG | S | Belongs to the UPF0340 family | ||
BCJHNJMD_00451 | 4e-84 | hmpT | S | ECF-type riboflavin transporter, S component | ||
BCJHNJMD_00452 | 6.9e-139 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | Phosphomethylpyrimidine kinase | |
BCJHNJMD_00453 | 1.1e-259 | norG_2 | K | Aminotransferase class I and II | ||
BCJHNJMD_00454 | 7.3e-222 | lytR5 | K | Cell envelope-related transcriptional attenuator domain | ||
BCJHNJMD_00455 | 2.2e-137 | P | ATPases associated with a variety of cellular activities | |||
BCJHNJMD_00456 | 3.8e-230 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
BCJHNJMD_00457 | 1.2e-222 | rodA | D | Cell cycle protein | ||
BCJHNJMD_00458 | 1.7e-96 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00459 | 1.1e-35 | hxlR | K | HxlR-like helix-turn-helix | ||
BCJHNJMD_00460 | 1.5e-53 | |||||
BCJHNJMD_00462 | 4.4e-70 | 4.4.1.5 | E | Glyoxalase | ||
BCJHNJMD_00463 | 1.9e-141 | S | Membrane | |||
BCJHNJMD_00464 | 2.8e-185 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
BCJHNJMD_00465 | 8.9e-172 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
BCJHNJMD_00466 | 4.4e-76 | |||||
BCJHNJMD_00467 | 2.7e-205 | gldA | 1.1.1.6 | C | dehydrogenase | |
BCJHNJMD_00468 | 4.2e-50 | ykkC | P | Small Multidrug Resistance protein | ||
BCJHNJMD_00469 | 4.8e-51 | sugE | P | Multidrug resistance protein | ||
BCJHNJMD_00470 | 1.4e-98 | speG | J | Acetyltransferase (GNAT) domain | ||
BCJHNJMD_00471 | 1.4e-145 | G | Belongs to the phosphoglycerate mutase family | |||
BCJHNJMD_00472 | 1.5e-18 | S | integral membrane protein | |||
BCJHNJMD_00473 | 0.0 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
BCJHNJMD_00474 | 2.9e-193 | nlhH_1 | I | alpha/beta hydrolase fold | ||
BCJHNJMD_00475 | 3.7e-249 | xylP2 | G | symporter | ||
BCJHNJMD_00476 | 1e-301 | E | ABC transporter, substratebinding protein | |||
BCJHNJMD_00477 | 1.9e-81 | |||||
BCJHNJMD_00478 | 1.6e-08 | |||||
BCJHNJMD_00479 | 5.8e-175 | K | Transcriptional regulator, LacI family | |||
BCJHNJMD_00480 | 1.1e-261 | G | Major Facilitator | |||
BCJHNJMD_00481 | 0.0 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
BCJHNJMD_00482 | 3.2e-135 | C | Zinc-binding dehydrogenase | |||
BCJHNJMD_00483 | 4.9e-114 | |||||
BCJHNJMD_00484 | 1.4e-74 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_00485 | 3.9e-54 | napB | K | Transcriptional regulator | ||
BCJHNJMD_00486 | 7e-111 | 1.6.5.5 | C | alcohol dehydrogenase | ||
BCJHNJMD_00487 | 3.6e-67 | 2.3.1.209, 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | ||
BCJHNJMD_00488 | 1.1e-50 | mdt(A) | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00489 | 1.2e-222 | C | Oxidoreductase | |||
BCJHNJMD_00490 | 9e-12 | |||||
BCJHNJMD_00491 | 3.4e-67 | K | Transcriptional regulator, HxlR family | |||
BCJHNJMD_00492 | 1.5e-208 | mccF | V | LD-carboxypeptidase | ||
BCJHNJMD_00493 | 3.6e-179 | rihB | 3.2.2.1, 3.2.2.8 | F | Nucleoside | |
BCJHNJMD_00494 | 5.8e-118 | yeiL | K | Cyclic nucleotide-monophosphate binding domain | ||
BCJHNJMD_00495 | 1.5e-172 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
BCJHNJMD_00496 | 6.3e-221 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
BCJHNJMD_00497 | 6.8e-124 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
BCJHNJMD_00498 | 1.1e-118 | S | GyrI-like small molecule binding domain | |||
BCJHNJMD_00499 | 3.7e-69 | ycgX | S | Protein of unknown function (DUF1398) | ||
BCJHNJMD_00500 | 6.8e-98 | S | Phosphatidylethanolamine-binding protein | |||
BCJHNJMD_00501 | 9.2e-224 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00502 | 1.9e-121 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
BCJHNJMD_00503 | 2.6e-181 | hrtB | V | ABC transporter permease | ||
BCJHNJMD_00504 | 2e-86 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
BCJHNJMD_00505 | 4.4e-206 | ynfM | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00506 | 6e-63 | G | Domain of unknown function (DUF386) | |||
BCJHNJMD_00507 | 2.7e-214 | G | Sugar (and other) transporter | |||
BCJHNJMD_00508 | 1.6e-82 | G | Domain of unknown function (DUF386) | |||
BCJHNJMD_00509 | 4.6e-129 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
BCJHNJMD_00510 | 5e-146 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
BCJHNJMD_00511 | 1.5e-235 | 2.7.1.53 | G | Xylulose kinase | ||
BCJHNJMD_00512 | 1.1e-165 | |||||
BCJHNJMD_00513 | 1.3e-155 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BCJHNJMD_00514 | 7.2e-141 | K | helix_turn _helix lactose operon repressor | |||
BCJHNJMD_00515 | 3.4e-83 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
BCJHNJMD_00516 | 1.5e-167 | mleP | S | Sodium Bile acid symporter family | ||
BCJHNJMD_00517 | 7.2e-308 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
BCJHNJMD_00518 | 4.2e-161 | mleR | K | LysR family | ||
BCJHNJMD_00520 | 6.6e-238 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_00521 | 5.9e-146 | K | Helix-turn-helix domain, rpiR family | |||
BCJHNJMD_00522 | 5.2e-217 | aguA | 3.5.3.12 | E | agmatine deiminase | |
BCJHNJMD_00523 | 3.5e-166 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
BCJHNJMD_00524 | 1.1e-216 | aguA | 3.5.3.12 | E | agmatine deiminase | |
BCJHNJMD_00525 | 3.8e-233 | aguD | E | Amino Acid | ||
BCJHNJMD_00526 | 2.5e-197 | ptcA | 2.1.3.3, 2.1.3.6 | 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 | |
BCJHNJMD_00527 | 3.1e-238 | nhaC | C | Na H antiporter NhaC | ||
BCJHNJMD_00528 | 6.8e-262 | E | Amino acid permease | |||
BCJHNJMD_00529 | 0.0 | tdc | 4.1.1.25 | E | Pyridoxal-dependent decarboxylase conserved domain | |
BCJHNJMD_00530 | 1.2e-238 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
BCJHNJMD_00531 | 1.3e-38 | |||||
BCJHNJMD_00534 | 1.4e-207 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
BCJHNJMD_00535 | 1.9e-26 | |||||
BCJHNJMD_00536 | 3.1e-156 | EG | EamA-like transporter family | |||
BCJHNJMD_00537 | 5.4e-302 | abfA | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
BCJHNJMD_00538 | 3.6e-39 | |||||
BCJHNJMD_00539 | 6.4e-14 | S | Transglycosylase associated protein | |||
BCJHNJMD_00540 | 3.6e-14 | yjdF | S | Protein of unknown function (DUF2992) | ||
BCJHNJMD_00541 | 1.7e-154 | K | Transcriptional regulator | |||
BCJHNJMD_00542 | 5.3e-305 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
BCJHNJMD_00543 | 7.1e-138 | S | Belongs to the UPF0246 family | |||
BCJHNJMD_00544 | 4.6e-109 | 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) | |
BCJHNJMD_00545 | 1.9e-119 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
BCJHNJMD_00546 | 8.3e-216 | naiP | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00547 | 5.3e-130 | S | Protein of unknown function | |||
BCJHNJMD_00548 | 1.5e-169 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
BCJHNJMD_00549 | 2.7e-160 | G | Belongs to the carbohydrate kinase PfkB family | |||
BCJHNJMD_00550 | 1.4e-251 | F | Belongs to the purine-cytosine permease (2.A.39) family | |||
BCJHNJMD_00551 | 1.2e-185 | yegU | O | ADP-ribosylglycohydrolase | ||
BCJHNJMD_00552 | 1.2e-118 | yihL | K | UTRA | ||
BCJHNJMD_00553 | 7.6e-37 | yhaZ | L | DNA alkylation repair enzyme | ||
BCJHNJMD_00556 | 3e-13 | yhaZ | L | DNA alkylation repair enzyme | ||
BCJHNJMD_00557 | 2.5e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
BCJHNJMD_00558 | 0.0 | tetP | J | elongation factor G | ||
BCJHNJMD_00559 | 8.1e-232 | EK | Aminotransferase, class I | |||
BCJHNJMD_00560 | 1.2e-23 | |||||
BCJHNJMD_00561 | 4.9e-208 | G | Major Facilitator | |||
BCJHNJMD_00562 | 0.0 | 3.2.1.55 | GH51 | G | Right handed beta helix region | |
BCJHNJMD_00563 | 2.6e-134 | K | helix_turn_helix, arabinose operon control protein | |||
BCJHNJMD_00564 | 1.9e-71 | S | COG NOG18757 non supervised orthologous group | |||
BCJHNJMD_00565 | 1.3e-202 | pmrB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00566 | 1.4e-157 | C | Aldo keto reductase | |||
BCJHNJMD_00567 | 9.3e-107 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
BCJHNJMD_00568 | 2.4e-121 | |||||
BCJHNJMD_00569 | 1.9e-115 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
BCJHNJMD_00570 | 2.5e-222 | LO | Uncharacterized conserved protein (DUF2075) | |||
BCJHNJMD_00571 | 2e-26 | K | Transcriptional | |||
BCJHNJMD_00572 | 1.4e-72 | |||||
BCJHNJMD_00573 | 5.2e-305 | M | Mycoplasma protein of unknown function, DUF285 | |||
BCJHNJMD_00574 | 1.3e-46 | S | NADPH-dependent FMN reductase | |||
BCJHNJMD_00575 | 3.1e-159 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | M | MucBP domain | |
BCJHNJMD_00576 | 1.6e-42 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BCJHNJMD_00577 | 1.4e-54 | azoR | C | Catalyzes the reductive cleavage of azo bond in aromatic azo compounds to the corresponding amines. Requires NADH, but not NADPH, as an electron donor for its activity | ||
BCJHNJMD_00578 | 5.4e-134 | lmrB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00579 | 4.6e-63 | 1.6.5.2 | S | NADPH-dependent FMN reductase | ||
BCJHNJMD_00580 | 2e-37 | T | Cyclic nucleotide-binding protein | |||
BCJHNJMD_00581 | 1.8e-274 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
BCJHNJMD_00582 | 7.4e-237 | xynP | G | MFS/sugar transport protein | ||
BCJHNJMD_00583 | 2.6e-87 | K | AraC-like ligand binding domain | |||
BCJHNJMD_00585 | 9.2e-58 | K | MarR family | |||
BCJHNJMD_00586 | 6.6e-140 | S | Alpha/beta hydrolase family | |||
BCJHNJMD_00588 | 5.8e-178 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
BCJHNJMD_00589 | 4.9e-47 | C | Flavodoxin | |||
BCJHNJMD_00590 | 2.9e-57 | adhR | K | MerR, DNA binding | ||
BCJHNJMD_00591 | 8.1e-77 | GM | NmrA-like family | |||
BCJHNJMD_00592 | 1.9e-102 | S | Alpha beta hydrolase | |||
BCJHNJMD_00593 | 7.6e-62 | yliE | T | EAL domain | ||
BCJHNJMD_00594 | 4e-28 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_00595 | 4.9e-50 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_00596 | 5e-134 | 1.1.1.219 | GM | Male sterility protein | ||
BCJHNJMD_00597 | 3.4e-172 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
BCJHNJMD_00598 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
BCJHNJMD_00599 | 2.4e-69 | K | Transcriptional regulator | |||
BCJHNJMD_00600 | 1.5e-94 | qorB | 1.6.5.2 | GM | NmrA-like family | |
BCJHNJMD_00601 | 3.8e-190 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
BCJHNJMD_00602 | 4.2e-141 | K | Helix-turn-helix domain | |||
BCJHNJMD_00603 | 1.5e-166 | |||||
BCJHNJMD_00604 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
BCJHNJMD_00605 | 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 | |
BCJHNJMD_00606 | 1.2e-216 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BCJHNJMD_00607 | 4e-184 | xynD | 3.5.1.104 | G | polysaccharide deacetylase | |
BCJHNJMD_00608 | 1.3e-58 | |||||
BCJHNJMD_00609 | 4.6e-103 | GM | NAD(P)H-binding | |||
BCJHNJMD_00610 | 4.1e-181 | iolS | C | Aldo keto reductase | ||
BCJHNJMD_00611 | 5.9e-228 | pbuG | S | permease | ||
BCJHNJMD_00612 | 5e-93 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BCJHNJMD_00613 | 1.5e-161 | drrA | V | ABC transporter | ||
BCJHNJMD_00614 | 7e-120 | drrB | U | ABC-2 type transporter | ||
BCJHNJMD_00615 | 1.4e-167 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
BCJHNJMD_00616 | 0.0 | S | Bacterial membrane protein YfhO | |||
BCJHNJMD_00617 | 1.2e-86 | ccl | S | QueT transporter | ||
BCJHNJMD_00619 | 1.1e-10 | |||||
BCJHNJMD_00620 | 2.9e-44 | M | hydrolase, family 25 | |||
BCJHNJMD_00621 | 4.4e-29 | |||||
BCJHNJMD_00622 | 7.5e-159 | S | Bacterial SH3 domain | |||
BCJHNJMD_00623 | 7e-29 | M | hydrolase, family 25 | |||
BCJHNJMD_00624 | 1.2e-13 | |||||
BCJHNJMD_00626 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
BCJHNJMD_00627 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
BCJHNJMD_00628 | 6.3e-279 | xynT | G | MFS/sugar transport protein | ||
BCJHNJMD_00629 | 2.9e-141 | rhaS2 | K | Transcriptional regulator, AraC family | ||
BCJHNJMD_00630 | 3.7e-279 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
BCJHNJMD_00631 | 5.2e-22 | |||||
BCJHNJMD_00632 | 4.5e-149 | F | DNA/RNA non-specific endonuclease | |||
BCJHNJMD_00633 | 4.5e-89 | |||||
BCJHNJMD_00636 | 2.8e-85 | S | regulation of response to stimulus | |||
BCJHNJMD_00638 | 1.8e-50 | |||||
BCJHNJMD_00639 | 1.8e-23 | |||||
BCJHNJMD_00641 | 2.6e-112 | L | haloacid dehalogenase-like hydrolase | |||
BCJHNJMD_00642 | 8.6e-251 | pepC | 3.4.22.40 | E | aminopeptidase | |
BCJHNJMD_00643 | 8.9e-78 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BCJHNJMD_00644 | 4.2e-109 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
BCJHNJMD_00645 | 4.5e-217 | tcaB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00646 | 1.6e-224 | S | module of peptide synthetase | |||
BCJHNJMD_00647 | 1.2e-91 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
BCJHNJMD_00648 | 1.4e-98 | J | Acetyltransferase (GNAT) domain | |||
BCJHNJMD_00649 | 4.8e-114 | ywnB | S | NAD(P)H-binding | ||
BCJHNJMD_00650 | 9.3e-245 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
BCJHNJMD_00651 | 1.4e-35 | |||||
BCJHNJMD_00652 | 5.4e-124 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
BCJHNJMD_00653 | 3e-37 | |||||
BCJHNJMD_00654 | 4.4e-54 | |||||
BCJHNJMD_00655 | 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 | ||
BCJHNJMD_00656 | 3.2e-256 | 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 | ||
BCJHNJMD_00657 | 5.9e-111 | jag | S | R3H domain protein | ||
BCJHNJMD_00658 | 1e-145 | 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 | ||
BCJHNJMD_00659 | 3.2e-59 | 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 | |
BCJHNJMD_00660 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
BCJHNJMD_00661 | 1.7e-257 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
BCJHNJMD_00662 | 8.5e-207 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
BCJHNJMD_00663 | 2e-35 | yaaA | S | S4 domain protein YaaA | ||
BCJHNJMD_00664 | 1.7e-210 | 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 | ||
BCJHNJMD_00665 | 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 | |
BCJHNJMD_00666 | 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 | |
BCJHNJMD_00667 | 1.9e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
BCJHNJMD_00668 | 3e-59 | 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 | ||
BCJHNJMD_00669 | 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 | ||
BCJHNJMD_00670 | 9.8e-230 | Q | Imidazolonepropionase and related amidohydrolases | |||
BCJHNJMD_00671 | 4.2e-300 | E | ABC transporter, substratebinding protein | |||
BCJHNJMD_00672 | 9.5e-141 | |||||
BCJHNJMD_00673 | 9.1e-228 | Q | Imidazolonepropionase and related amidohydrolases | |||
BCJHNJMD_00674 | 3.7e-301 | E | ABC transporter, substratebinding protein | |||
BCJHNJMD_00675 | 2.2e-99 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_00676 | 2.5e-74 | S | membrane transporter protein | |||
BCJHNJMD_00677 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
BCJHNJMD_00678 | 7.2e-64 | rplI | J | Binds to the 23S rRNA | ||
BCJHNJMD_00681 | 6.6e-255 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
BCJHNJMD_00682 | 3.8e-101 | S | NADPH-dependent FMN reductase | |||
BCJHNJMD_00683 | 1.3e-210 | yttB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00684 | 2.9e-20 | |||||
BCJHNJMD_00685 | 1.2e-302 | E | ABC transporter, substratebinding protein | |||
BCJHNJMD_00686 | 1.7e-35 | |||||
BCJHNJMD_00687 | 2.4e-112 | E | Matrixin | |||
BCJHNJMD_00689 | 5.7e-132 | K | response regulator | |||
BCJHNJMD_00690 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
BCJHNJMD_00691 | 4.8e-238 | yycH | S | YycH protein | ||
BCJHNJMD_00692 | 6.1e-149 | yycI | S | YycH protein | ||
BCJHNJMD_00693 | 3.4e-157 | vicX | 3.1.26.11 | S | domain protein | |
BCJHNJMD_00694 | 3.4e-194 | htrA | 3.4.21.107 | O | serine protease | |
BCJHNJMD_00695 | 2.1e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
BCJHNJMD_00696 | 6.4e-13 | |||||
BCJHNJMD_00699 | 3.1e-30 | L | Phage terminase, small subunit | |||
BCJHNJMD_00700 | 2.7e-268 | S | Phage Terminase | |||
BCJHNJMD_00701 | 8.4e-37 | S | Phage portal protein | |||
BCJHNJMD_00702 | 5e-69 | S | Phage portal protein | |||
BCJHNJMD_00703 | 9.2e-82 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
BCJHNJMD_00704 | 3.2e-105 | S | Phage capsid family | |||
BCJHNJMD_00705 | 9.1e-11 | L | Phage gp6-like head-tail connector protein | |||
BCJHNJMD_00706 | 1.9e-32 | S | Phage head-tail joining protein | |||
BCJHNJMD_00707 | 3e-24 | S | Bacteriophage HK97-gp10, putative tail-component | |||
BCJHNJMD_00708 | 5.9e-30 | S | Protein of unknown function (DUF806) | |||
BCJHNJMD_00709 | 1.2e-74 | S | Phage tail tube protein | |||
BCJHNJMD_00710 | 1.3e-18 | S | Phage tail assembly chaperone proteins, TAC | |||
BCJHNJMD_00712 | 9.5e-226 | M | Phage tail tape measure protein TP901 | |||
BCJHNJMD_00713 | 9.5e-153 | S | Phage tail protein | |||
BCJHNJMD_00714 | 0.0 | S | Phage minor structural protein | |||
BCJHNJMD_00715 | 2.7e-23 | |||||
BCJHNJMD_00717 | 1.1e-56 | |||||
BCJHNJMD_00718 | 7.9e-30 | E | Leucine-rich repeat (LRR) protein | |||
BCJHNJMD_00719 | 3.3e-10 | 3.6.4.12 | L | UvrD/REP helicase N-terminal domain | ||
BCJHNJMD_00720 | 0.0 | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | ||
BCJHNJMD_00721 | 5.1e-306 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
BCJHNJMD_00722 | 5.1e-101 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
BCJHNJMD_00723 | 1.4e-198 | L | Psort location Cytoplasmic, score | |||
BCJHNJMD_00724 | 1.4e-30 | |||||
BCJHNJMD_00725 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
BCJHNJMD_00726 | 1.4e-66 | |||||
BCJHNJMD_00727 | 5.3e-153 | |||||
BCJHNJMD_00728 | 9.7e-59 | |||||
BCJHNJMD_00729 | 2.7e-269 | traK | U | TraM recognition site of TraD and TraG | ||
BCJHNJMD_00730 | 1.2e-77 | |||||
BCJHNJMD_00731 | 4.6e-53 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
BCJHNJMD_00732 | 9.6e-88 | |||||
BCJHNJMD_00733 | 1.7e-207 | M | CHAP domain | |||
BCJHNJMD_00734 | 3.3e-140 | polC | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | S | WXG100 protein secretion system (Wss), protein YukC |
BCJHNJMD_00736 | 1.5e-49 | repA | S | Replication initiator protein A | ||
BCJHNJMD_00737 | 3.3e-43 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
BCJHNJMD_00738 | 1.1e-86 | |||||
BCJHNJMD_00739 | 1.2e-40 | |||||
BCJHNJMD_00740 | 1.2e-26 | |||||
BCJHNJMD_00741 | 0.0 | traA | L | MobA MobL family protein | ||
BCJHNJMD_00742 | 9.5e-52 | |||||
BCJHNJMD_00743 | 1.7e-105 | |||||
BCJHNJMD_00744 | 5.1e-51 | S | Cag pathogenicity island, type IV secretory system | |||
BCJHNJMD_00745 | 8.6e-36 | |||||
BCJHNJMD_00746 | 8.1e-117 | |||||
BCJHNJMD_00747 | 0.0 | traE | U | type IV secretory pathway VirB4 | ||
BCJHNJMD_00748 | 7.8e-16 | |||||
BCJHNJMD_00749 | 1.2e-18 | |||||
BCJHNJMD_00750 | 6.1e-76 | L | Transposase and inactivated derivatives, IS30 family | |||
BCJHNJMD_00752 | 2.4e-11 | |||||
BCJHNJMD_00753 | 6.7e-19 | |||||
BCJHNJMD_00758 | 1.1e-149 | yjjH | S | Calcineurin-like phosphoesterase | ||
BCJHNJMD_00759 | 1.7e-298 | dtpT | U | amino acid peptide transporter | ||
BCJHNJMD_00760 | 1.4e-50 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
BCJHNJMD_00765 | 8.5e-22 | S | Domain of unknown function (DUF771) | |||
BCJHNJMD_00766 | 1.2e-24 | |||||
BCJHNJMD_00770 | 3.7e-14 | |||||
BCJHNJMD_00771 | 2.8e-42 | yvaO | K | Helix-turn-helix XRE-family like proteins | ||
BCJHNJMD_00772 | 1.4e-94 | 2.1.1.37 | L | C-5 cytosine-specific DNA methylase | ||
BCJHNJMD_00776 | 2.7e-41 | S | Endodeoxyribonuclease RusA | |||
BCJHNJMD_00777 | 1.5e-55 | K | AntA/AntB antirepressor | |||
BCJHNJMD_00778 | 1.9e-35 | 3.1.3.16 | L | DnaD domain protein | ||
BCJHNJMD_00780 | 4.7e-33 | |||||
BCJHNJMD_00782 | 5.1e-16 | |||||
BCJHNJMD_00783 | 4.2e-31 | |||||
BCJHNJMD_00784 | 7.8e-33 | XK27_10050 | K | Peptidase S24-like | ||
BCJHNJMD_00786 | 7.5e-34 | S | DNA binding | |||
BCJHNJMD_00787 | 1.7e-13 | |||||
BCJHNJMD_00792 | 6.5e-10 | |||||
BCJHNJMD_00798 | 3e-165 | L | Integrase core domain | |||
BCJHNJMD_00799 | 8.2e-110 | L | Bacterial dnaA protein | |||
BCJHNJMD_00800 | 3.2e-239 | 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) | |
BCJHNJMD_00801 | 6.6e-238 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BCJHNJMD_00802 | 1.7e-29 | |||||
BCJHNJMD_00803 | 1.1e-57 | K | Winged helix DNA-binding domain | |||
BCJHNJMD_00804 | 2.3e-251 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
BCJHNJMD_00805 | 4.9e-271 | frvR | K | Mga helix-turn-helix domain | ||
BCJHNJMD_00806 | 2.2e-35 | |||||
BCJHNJMD_00807 | 3.7e-252 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
BCJHNJMD_00808 | 4.9e-78 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
BCJHNJMD_00809 | 3.8e-84 | S | Bacterial PH domain | |||
BCJHNJMD_00810 | 2.6e-256 | ydbT | S | Bacterial PH domain | ||
BCJHNJMD_00811 | 1.2e-193 | yjcE | P | Sodium proton antiporter | ||
BCJHNJMD_00812 | 5.5e-206 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
BCJHNJMD_00813 | 7e-213 | EG | GntP family permease | |||
BCJHNJMD_00814 | 4.9e-193 | KT | Putative sugar diacid recognition | |||
BCJHNJMD_00815 | 2.4e-175 | |||||
BCJHNJMD_00816 | 1.7e-162 | ytrB | V | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00817 | 2.1e-61 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
BCJHNJMD_00818 | 1.5e-124 | S | Protein of unknown function (DUF975) | |||
BCJHNJMD_00819 | 1.3e-133 | XK27_07210 | 6.1.1.6 | S | B3/4 domain | |
BCJHNJMD_00820 | 0.0 | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | ||
BCJHNJMD_00821 | 6.9e-25 | |||||
BCJHNJMD_00822 | 2.8e-179 | xopQ | 3.2.2.1, 3.2.2.8 | F | inosine-uridine preferring nucleoside hydrolase | |
BCJHNJMD_00823 | 6e-166 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
BCJHNJMD_00824 | 2.1e-96 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
BCJHNJMD_00825 | 8e-46 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
BCJHNJMD_00826 | 7.6e-259 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
BCJHNJMD_00827 | 3.3e-145 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
BCJHNJMD_00828 | 1.1e-30 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
BCJHNJMD_00829 | 1.5e-111 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
BCJHNJMD_00830 | 5.7e-135 | mleP | S | Membrane transport protein | ||
BCJHNJMD_00831 | 3e-151 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
BCJHNJMD_00832 | 4e-109 | citR | K | Putative sugar-binding domain | ||
BCJHNJMD_00833 | 1.5e-82 | ydjP | I | Alpha/beta hydrolase family | ||
BCJHNJMD_00834 | 4.5e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00835 | 2.2e-159 | K | helix_turn_helix, arabinose operon control protein | |||
BCJHNJMD_00836 | 1.9e-209 | norA | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00837 | 2.7e-152 | K | LysR substrate binding domain | |||
BCJHNJMD_00838 | 6e-159 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
BCJHNJMD_00839 | 9.7e-101 | P | Cadmium resistance transporter | |||
BCJHNJMD_00840 | 2.1e-52 | czrA | K | Transcriptional regulator, ArsR family | ||
BCJHNJMD_00841 | 2.1e-311 | mco | Q | Multicopper oxidase | ||
BCJHNJMD_00842 | 5.6e-121 | S | SNARE associated Golgi protein | |||
BCJHNJMD_00843 | 1e-310 | cadA | P | P-type ATPase | ||
BCJHNJMD_00844 | 2.2e-185 | sdrF | M | Collagen binding domain | ||
BCJHNJMD_00845 | 5e-69 | S | Iron-sulphur cluster biosynthesis | |||
BCJHNJMD_00846 | 3.9e-60 | gntR1 | K | Transcriptional regulator, GntR family | ||
BCJHNJMD_00847 | 0.0 | Q | FtsX-like permease family | |||
BCJHNJMD_00848 | 1.8e-136 | cysA | V | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00849 | 7.2e-183 | S | Aldo keto reductase | |||
BCJHNJMD_00850 | 5.7e-201 | ytbD | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00851 | 6.3e-63 | K | Transcriptional regulator, HxlR family | |||
BCJHNJMD_00852 | 1.5e-164 | |||||
BCJHNJMD_00853 | 0.0 | 2.7.8.12 | M | glycerophosphotransferase | ||
BCJHNJMD_00854 | 5.3e-72 | K | Transcriptional regulator | |||
BCJHNJMD_00855 | 2.6e-152 | 1.6.5.2 | GM | NmrA-like family | ||
BCJHNJMD_00856 | 5.5e-133 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BCJHNJMD_00857 | 2.8e-151 | 3.2.1.37 | GH43 | K | helix_turn_helix, arabinose operon control protein | |
BCJHNJMD_00858 | 0.0 | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family | |
BCJHNJMD_00859 | 6.8e-226 | G | Major Facilitator | |||
BCJHNJMD_00860 | 3.3e-124 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BCJHNJMD_00861 | 1.2e-97 | S | membrane transporter protein | |||
BCJHNJMD_00862 | 2e-286 | E | dipeptidase activity | |||
BCJHNJMD_00863 | 8.1e-154 | K | acetyltransferase | |||
BCJHNJMD_00864 | 7.7e-143 | iap | CBM50 | M | NlpC/P60 family | |
BCJHNJMD_00865 | 2.7e-73 | spx4 | 1.20.4.1 | P | ArsC family | |
BCJHNJMD_00866 | 9.9e-250 | yclG | M | Parallel beta-helix repeats | ||
BCJHNJMD_00867 | 4.6e-64 | K | MarR family | |||
BCJHNJMD_00868 | 8.1e-151 | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
BCJHNJMD_00869 | 5.7e-160 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BCJHNJMD_00870 | 1.4e-152 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
BCJHNJMD_00871 | 2.3e-41 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
BCJHNJMD_00872 | 5.4e-77 | |||||
BCJHNJMD_00873 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
BCJHNJMD_00874 | 1.3e-254 | malT | G | Major Facilitator | ||
BCJHNJMD_00875 | 1.8e-181 | malR | K | Transcriptional regulator, LacI family | ||
BCJHNJMD_00876 | 7.9e-244 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
BCJHNJMD_00877 | 1.2e-123 | K | cheY-homologous receiver domain | |||
BCJHNJMD_00878 | 0.0 | S | membrane | |||
BCJHNJMD_00880 | 1.6e-168 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
BCJHNJMD_00881 | 8.1e-28 | S | Protein of unknown function (DUF2929) | |||
BCJHNJMD_00882 | 8.9e-95 | 2.7.6.5 | S | RelA SpoT domain protein | ||
BCJHNJMD_00883 | 6.8e-226 | mdtG | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00884 | 7.8e-140 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
BCJHNJMD_00885 | 2e-56 | ywjH | S | Protein of unknown function (DUF1634) | ||
BCJHNJMD_00886 | 7.6e-144 | yxaA | S | membrane transporter protein | ||
BCJHNJMD_00887 | 1e-156 | lysR5 | K | LysR substrate binding domain | ||
BCJHNJMD_00888 | 2.1e-168 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
BCJHNJMD_00889 | 1.7e-246 | pts14C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
BCJHNJMD_00890 | 1.2e-162 | |||||
BCJHNJMD_00891 | 3.3e-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) | |
BCJHNJMD_00892 | 7.4e-163 | I | Carboxylesterase family | |||
BCJHNJMD_00893 | 2.7e-149 | M1-1017 | ||||
BCJHNJMD_00894 | 5.4e-59 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BCJHNJMD_00895 | 3.5e-59 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
BCJHNJMD_00896 | 1.3e-38 | yrkD | S | Metal-sensitive transcriptional repressor | ||
BCJHNJMD_00897 | 2.3e-56 | trxA1 | O | Belongs to the thioredoxin family | ||
BCJHNJMD_00898 | 1.7e-268 | nox | C | NADH oxidase | ||
BCJHNJMD_00899 | 8.2e-154 | S | Uncharacterised protein, DegV family COG1307 | |||
BCJHNJMD_00900 | 6.4e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BCJHNJMD_00901 | 8e-129 | IQ | reductase | |||
BCJHNJMD_00902 | 1.4e-39 | |||||
BCJHNJMD_00903 | 4.2e-81 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
BCJHNJMD_00904 | 2.2e-110 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BCJHNJMD_00905 | 7e-128 | kdgT | P | 2-keto-3-deoxygluconate permease | ||
BCJHNJMD_00906 | 1.2e-138 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BCJHNJMD_00907 | 6.2e-146 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
BCJHNJMD_00909 | 6.2e-10 | |||||
BCJHNJMD_00910 | 1.9e-53 | kguE | 2.7.1.45 | G | Xylose isomerase-like TIM barrel | |
BCJHNJMD_00911 | 1.2e-100 | K | Bacterial transcriptional regulator | |||
BCJHNJMD_00912 | 9.1e-267 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
BCJHNJMD_00913 | 2.2e-102 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_00914 | 2.4e-95 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
BCJHNJMD_00915 | 4.2e-228 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
BCJHNJMD_00916 | 1.9e-115 | ylbE | GM | NAD(P)H-binding | ||
BCJHNJMD_00917 | 1.2e-30 | |||||
BCJHNJMD_00918 | 1.5e-129 | K | Transcriptional regulatory protein, C terminal | |||
BCJHNJMD_00919 | 1.7e-246 | T | PhoQ Sensor | |||
BCJHNJMD_00920 | 6.5e-43 | |||||
BCJHNJMD_00921 | 9.2e-66 | |||||
BCJHNJMD_00922 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
BCJHNJMD_00923 | 1.6e-150 | corA | P | CorA-like Mg2+ transporter protein | ||
BCJHNJMD_00924 | 7.3e-138 | pnuC | H | nicotinamide mononucleotide transporter | ||
BCJHNJMD_00925 | 5.6e-56 | K | Winged helix DNA-binding domain | |||
BCJHNJMD_00926 | 0.0 | malL | 3.2.1.10, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31 | G | Alpha amylase, catalytic domain protein |
BCJHNJMD_00927 | 2.4e-121 | yclH | V | ABC transporter | ||
BCJHNJMD_00928 | 5.5e-166 | yclI | V | FtsX-like permease family | ||
BCJHNJMD_00929 | 3.1e-196 | yubA | S | AI-2E family transporter | ||
BCJHNJMD_00930 | 6.9e-105 | |||||
BCJHNJMD_00931 | 2.9e-246 | M | hydrolase, family 25 | |||
BCJHNJMD_00932 | 2.2e-193 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
BCJHNJMD_00933 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
BCJHNJMD_00934 | 1.2e-109 | M | Protein of unknown function (DUF3737) | |||
BCJHNJMD_00935 | 3.5e-224 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
BCJHNJMD_00936 | 5.5e-183 | yfeX | P | Peroxidase | ||
BCJHNJMD_00937 | 5e-221 | mdtG | EGP | Major facilitator Superfamily | ||
BCJHNJMD_00938 | 4.6e-45 | |||||
BCJHNJMD_00939 | 2.8e-224 | opuCA | E | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00940 | 8e-106 | opuCB | E | ABC transporter permease | ||
BCJHNJMD_00941 | 2e-177 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BCJHNJMD_00942 | 2.1e-109 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
BCJHNJMD_00943 | 8.7e-211 | |||||
BCJHNJMD_00944 | 1.9e-262 | |||||
BCJHNJMD_00945 | 5e-66 | S | Tautomerase enzyme | |||
BCJHNJMD_00946 | 0.0 | uvrA2 | L | ABC transporter | ||
BCJHNJMD_00947 | 4.6e-99 | S | Protein of unknown function (DUF1440) | |||
BCJHNJMD_00948 | 8.1e-249 | xylP1 | G | MFS/sugar transport protein | ||
BCJHNJMD_00949 | 2.4e-94 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BCJHNJMD_00950 | 1.8e-37 | |||||
BCJHNJMD_00951 | 6e-67 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
BCJHNJMD_00952 | 2.4e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
BCJHNJMD_00953 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
BCJHNJMD_00954 | 9.5e-122 | |||||
BCJHNJMD_00955 | 0.0 | oatA | I | Acyltransferase | ||
BCJHNJMD_00956 | 2.5e-189 | 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 | |
BCJHNJMD_00957 | 9e-158 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
BCJHNJMD_00958 | 9.6e-155 | yxkH | G | Polysaccharide deacetylase | ||
BCJHNJMD_00960 | 2.5e-67 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
BCJHNJMD_00961 | 0.0 | ctpA | 3.6.3.54 | P | P-type ATPase | |
BCJHNJMD_00962 | 3.8e-159 | S | reductase | |||
BCJHNJMD_00963 | 2e-225 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
BCJHNJMD_00964 | 1.9e-77 | copR | K | Copper transport repressor CopY TcrY | ||
BCJHNJMD_00965 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
BCJHNJMD_00966 | 1.3e-168 | EG | EamA-like transporter family | |||
BCJHNJMD_00967 | 5e-119 | S | Elongation factor G-binding protein, N-terminal | |||
BCJHNJMD_00968 | 4.3e-98 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
BCJHNJMD_00969 | 3.3e-154 | |||||
BCJHNJMD_00970 | 7.5e-277 | pipD | E | Dipeptidase | ||
BCJHNJMD_00971 | 0.0 | pacL1 | P | P-type ATPase | ||
BCJHNJMD_00972 | 9.2e-73 | K | MarR family | |||
BCJHNJMD_00973 | 4.9e-99 | S | NADPH-dependent FMN reductase | |||
BCJHNJMD_00974 | 3.5e-197 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
BCJHNJMD_00975 | 6.4e-12 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BCJHNJMD_00976 | 7.2e-270 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
BCJHNJMD_00977 | 1.2e-163 | opuBA | E | ABC transporter, ATP-binding protein | ||
BCJHNJMD_00978 | 4.4e-68 | lrpA | K | AsnC family | ||
BCJHNJMD_00979 | 3e-187 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
BCJHNJMD_00980 | 3.7e-224 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BCJHNJMD_00981 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BCJHNJMD_00982 | 1.5e-64 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_00983 | 1.3e-106 | |||||
BCJHNJMD_00984 | 4.9e-241 | yifK | E | Amino acid permease | ||
BCJHNJMD_00985 | 2.8e-96 | K | Acetyltransferase (GNAT) domain | |||
BCJHNJMD_00986 | 1.6e-71 | fld | C | Flavodoxin | ||
BCJHNJMD_00987 | 5.4e-220 | fabV | 1.3.1.44, 1.3.1.9 | I | NAD(P)H binding domain of trans-2-enoyl-CoA reductase | |
BCJHNJMD_00988 | 1.9e-186 | 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 | ||
BCJHNJMD_00989 | 3.5e-113 | S | Putative adhesin | |||
BCJHNJMD_00990 | 6.3e-74 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
BCJHNJMD_00991 | 2.7e-54 | K | Transcriptional regulator PadR-like family | |||
BCJHNJMD_00992 | 3.8e-104 | pncA | Q | Isochorismatase family | ||
BCJHNJMD_00993 | 1.4e-216 | srfJ1 | 3.2.1.45 | GH30 | M | Belongs to the glycosyl hydrolase 30 family |
BCJHNJMD_00994 | 5e-147 | blt | G | MFS/sugar transport protein | ||
BCJHNJMD_00995 | 6.6e-247 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
BCJHNJMD_00996 | 3.4e-78 | K | AraC-like ligand binding domain | |||
BCJHNJMD_00997 | 8.4e-243 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
BCJHNJMD_00998 | 2.4e-161 | G | Peptidase_C39 like family | |||
BCJHNJMD_00999 | 4.5e-199 | M | NlpC/P60 family | |||
BCJHNJMD_01000 | 2.1e-293 | 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 | |
BCJHNJMD_01001 | 1.5e-112 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
BCJHNJMD_01002 | 3.7e-38 | |||||
BCJHNJMD_01003 | 6.9e-133 | puuD | S | peptidase C26 | ||
BCJHNJMD_01004 | 2.9e-119 | S | Membrane | |||
BCJHNJMD_01005 | 0.0 | O | Pro-kumamolisin, activation domain | |||
BCJHNJMD_01006 | 1.8e-164 | I | Alpha beta | |||
BCJHNJMD_01007 | 8.4e-148 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
BCJHNJMD_01008 | 4.3e-180 | D | Alpha beta | |||
BCJHNJMD_01009 | 4.3e-98 | fadR | K | Bacterial regulatory proteins, tetR family | ||
BCJHNJMD_01010 | 4e-122 | GM | NmrA-like family | |||
BCJHNJMD_01011 | 2.3e-233 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
BCJHNJMD_01012 | 9.8e-26 | GM | NmrA-like family | |||
BCJHNJMD_01013 | 4.6e-241 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
BCJHNJMD_01014 | 3.7e-251 | 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 | |
BCJHNJMD_01015 | 3.2e-186 | 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 | |
BCJHNJMD_01016 | 1.1e-122 | XK27_00720 | S | regulation of response to stimulus | ||
BCJHNJMD_01017 | 2.4e-276 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
BCJHNJMD_01018 | 1.5e-71 | T | Universal stress protein family | |||
BCJHNJMD_01019 | 3.1e-121 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
BCJHNJMD_01020 | 1.6e-89 | P | Cadmium resistance transporter | |||
BCJHNJMD_01021 | 1.1e-90 | |||||
BCJHNJMD_01022 | 4.6e-73 | |||||
BCJHNJMD_01023 | 2.1e-79 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
BCJHNJMD_01024 | 6.7e-75 | elaA | S | Gnat family | ||
BCJHNJMD_01025 | 2.2e-185 | 1.1.1.219 | GM | Male sterility protein | ||
BCJHNJMD_01026 | 4.5e-100 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_01027 | 9.9e-83 | padR | K | Virulence activator alpha C-term | ||
BCJHNJMD_01028 | 3.2e-103 | padC | Q | Phenolic acid decarboxylase | ||
BCJHNJMD_01030 | 6.4e-84 | F | NUDIX domain | |||
BCJHNJMD_01032 | 3.4e-94 | wecD | K | Acetyltransferase (GNAT) family | ||
BCJHNJMD_01033 | 4e-124 | yliE | T | Putative diguanylate phosphodiesterase | ||
BCJHNJMD_01034 | 1.4e-101 | XK27_06935 | K | Bacterial regulatory proteins, tetR family | ||
BCJHNJMD_01035 | 4.1e-176 | S | ABC-2 family transporter protein | |||
BCJHNJMD_01036 | 3e-125 | malR3 | K | cheY-homologous receiver domain | ||
BCJHNJMD_01037 | 1.3e-269 | yufL | 2.7.13.3 | T | Single cache domain 3 | |
BCJHNJMD_01038 | 6e-188 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BCJHNJMD_01039 | 2.3e-190 | S | Membrane transport protein | |||
BCJHNJMD_01040 | 3.2e-251 | nhaC | C | Na H antiporter NhaC | ||
BCJHNJMD_01041 | 1.3e-93 | Z012_06855 | S | Acetyltransferase (GNAT) family | ||
BCJHNJMD_01042 | 7.5e-70 | |||||
BCJHNJMD_01043 | 1.3e-167 | C | Aldo keto reductase | |||
BCJHNJMD_01044 | 2.3e-49 | |||||
BCJHNJMD_01045 | 3.3e-122 | kcsA | P | Ion channel | ||
BCJHNJMD_01046 | 1.1e-217 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BCJHNJMD_01047 | 3e-95 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
BCJHNJMD_01048 | 1.1e-89 | uspA | T | universal stress protein | ||
BCJHNJMD_01049 | 0.0 | S | membrane | |||
BCJHNJMD_01050 | 1e-68 | frataxin | S | Domain of unknown function (DU1801) | ||
BCJHNJMD_01051 | 3.3e-141 | IQ | reductase | |||
BCJHNJMD_01052 | 3.8e-225 | xylT | EGP | Major facilitator Superfamily | ||
BCJHNJMD_01053 | 2.8e-290 | xylB | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | Xylulose kinase | |
BCJHNJMD_01054 | 2.3e-267 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
BCJHNJMD_01056 | 6.2e-18 | |||||
BCJHNJMD_01057 | 5.2e-49 | |||||
BCJHNJMD_01058 | 5.2e-69 | |||||
BCJHNJMD_01059 | 1.6e-196 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
BCJHNJMD_01060 | 1.6e-79 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
BCJHNJMD_01061 | 2.4e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
BCJHNJMD_01062 | 3.2e-178 | oppF | P | Belongs to the ABC transporter superfamily | ||
BCJHNJMD_01063 | 9.8e-180 | oppB | P | ABC transporter permease | ||
BCJHNJMD_01064 | 1e-173 | oppC | EP | Binding-protein-dependent transport system inner membrane component | ||
BCJHNJMD_01065 | 0.0 | oppA1 | E | ABC transporter substrate-binding protein | ||
BCJHNJMD_01066 | 2.4e-50 | K | transcriptional regulator | |||
BCJHNJMD_01067 | 1.1e-165 | norB | EGP | Major Facilitator | ||
BCJHNJMD_01068 | 5.3e-52 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
BCJHNJMD_01069 | 1.6e-174 | L | Transposase and inactivated derivatives, IS30 family | |||
BCJHNJMD_01071 | 2.9e-120 | Z012_12235 | S | Baseplate J-like protein | ||
BCJHNJMD_01073 | 2.7e-27 | |||||
BCJHNJMD_01074 | 4.5e-81 | |||||
BCJHNJMD_01075 | 2e-10 | |||||
BCJHNJMD_01076 | 9.1e-42 | M | LysM domain | |||
BCJHNJMD_01077 | 1.3e-97 | M | Phage tail tape measure protein TP901 | |||
BCJHNJMD_01080 | 1.3e-07 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
BCJHNJMD_01084 | 2.8e-31 | |||||
BCJHNJMD_01086 | 1.4e-73 | gpG | ||||
BCJHNJMD_01087 | 1.5e-16 | S | Domain of unknown function (DUF4355) | |||
BCJHNJMD_01088 | 1.5e-66 | S | head morphogenesis protein, SPP1 gp7 family | |||
BCJHNJMD_01089 | 6.8e-147 | S | Phage portal protein, SPP1 Gp6-like | |||
BCJHNJMD_01090 | 5.8e-140 | ps334 | S | Terminase-like family | ||
BCJHNJMD_01091 | 8.2e-42 | ps333 | L | Terminase small subunit | ||
BCJHNJMD_01096 | 2.7e-10 | |||||
BCJHNJMD_01097 | 4.6e-70 | tnp2PF3 | L | manually curated | ||
BCJHNJMD_01098 | 7e-54 | L | recombinase activity | |||
BCJHNJMD_01100 | 3.4e-15 | |||||
BCJHNJMD_01103 | 1.7e-152 | L | Integrase core domain | |||
BCJHNJMD_01104 | 2.6e-37 | yvaO | K | Helix-turn-helix XRE-family like proteins | ||
BCJHNJMD_01105 | 1.8e-14 | XK27_07105 | K | Helix-turn-helix domain | ||
BCJHNJMD_01107 | 3.3e-16 | |||||
BCJHNJMD_01113 | 8.1e-88 | |||||
BCJHNJMD_01114 | 1.5e-206 | Z012_12235 | S | Baseplate J-like protein | ||
BCJHNJMD_01115 | 4.2e-62 | S | Protein of unknown function (DUF2634) | |||
BCJHNJMD_01116 | 1.4e-65 | |||||
BCJHNJMD_01117 | 8e-174 | |||||
BCJHNJMD_01118 | 2.6e-67 | |||||
BCJHNJMD_01119 | 8.9e-176 | M | LysM domain | |||
BCJHNJMD_01120 | 0.0 | M | Phage tail tape measure protein TP901 | |||
BCJHNJMD_01122 | 7.9e-13 | |||||
BCJHNJMD_01123 | 8.3e-87 | |||||
BCJHNJMD_01124 | 2.3e-204 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
BCJHNJMD_01125 | 7.9e-69 | |||||
BCJHNJMD_01126 | 4.7e-08 | |||||
BCJHNJMD_01128 | 1e-82 | |||||
BCJHNJMD_01130 | 5.2e-201 | S | Phage major capsid protein E | |||
BCJHNJMD_01131 | 1.5e-65 | |||||
BCJHNJMD_01132 | 6.3e-77 | S | Domain of unknown function (DUF4355) | |||
BCJHNJMD_01133 | 3.4e-169 | S | head morphogenesis protein, SPP1 gp7 family | |||
BCJHNJMD_01134 | 3.8e-279 | S | Phage portal protein, SPP1 Gp6-like | |||
BCJHNJMD_01135 | 1.5e-250 | S | Terminase-like family | |||
BCJHNJMD_01136 | 1e-18 | S | HicA toxin of bacterial toxin-antitoxin, | |||
BCJHNJMD_01137 | 2e-41 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
BCJHNJMD_01138 | 2e-106 | L | Integrase | |||
BCJHNJMD_01139 | 6.8e-136 | xtmA | L | Terminase small subunit | ||
BCJHNJMD_01141 | 2.6e-52 | |||||
BCJHNJMD_01146 | 1e-78 | arpU | S | Phage transcriptional regulator, ArpU family | ||
BCJHNJMD_01152 | 1.4e-17 | |||||
BCJHNJMD_01155 | 4.9e-25 | |||||
BCJHNJMD_01157 | 9e-32 | |||||
BCJHNJMD_01158 | 1.2e-31 | |||||
BCJHNJMD_01159 | 7e-75 | S | Protein of unknown function (DUF1064) | |||
BCJHNJMD_01160 | 1.3e-26 | S | YopX protein | |||
BCJHNJMD_01161 | 3.7e-24 | M | Bacterial Ig-like domain (group 3) | |||
BCJHNJMD_01164 | 9.4e-100 | tnp | L | DDE domain | ||
BCJHNJMD_01166 | 1.9e-28 | L | Transposase and inactivated derivatives, IS30 family | |||
BCJHNJMD_01167 | 3.7e-105 | L | Transposase and inactivated derivatives, IS30 family | |||
BCJHNJMD_01168 | 9.2e-07 | K | MarR family | |||
BCJHNJMD_01170 | 3.5e-104 | |||||
BCJHNJMD_01173 | 1e-40 | |||||
BCJHNJMD_01174 | 2.4e-142 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
BCJHNJMD_01175 | 5.5e-38 | K | DNA-binding helix-turn-helix protein | |||
BCJHNJMD_01176 | 2.6e-26 | L | Transposase and inactivated derivatives, IS30 family | |||
BCJHNJMD_01177 | 4.5e-59 | M | Glycosyl transferases group 1 | |||
BCJHNJMD_01178 | 2.9e-51 | M | -O-antigen | |||
BCJHNJMD_01179 | 1.9e-83 | cps2J | S | Polysaccharide biosynthesis protein | ||
BCJHNJMD_01180 | 5.1e-67 | wcmJ | S | SPTR Capsular exopolysaccharide biosynthesis protein (Wzm) | ||
BCJHNJMD_01181 | 1.8e-153 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BCJHNJMD_01182 | 3.6e-165 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
BCJHNJMD_01183 | 8.8e-147 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
BCJHNJMD_01184 | 9.6e-180 | pdxB | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
BCJHNJMD_01185 | 2.7e-282 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
BCJHNJMD_01186 | 1.1e-173 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
BCJHNJMD_01187 | 2.4e-269 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
BCJHNJMD_01188 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
BCJHNJMD_01189 | 3.5e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
BCJHNJMD_01190 | 1e-154 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
BCJHNJMD_01191 | 5.1e-99 | 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 | |
BCJHNJMD_01192 | 7.2e-214 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
BCJHNJMD_01193 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
BCJHNJMD_01194 | 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 | |
BCJHNJMD_01195 | 1.1e-193 | camS | S | sex pheromone | ||
BCJHNJMD_01196 | 1.5e-49 | 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) | |
BCJHNJMD_01197 | 1.9e-275 | 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) | |
BCJHNJMD_01198 | 6.5e-273 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
BCJHNJMD_01199 | 9.4e-189 | yegS | 2.7.1.107 | G | Lipid kinase | |
BCJHNJMD_01200 | 6.3e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
BCJHNJMD_01201 | 3.3e-42 | eutP | E | Ethanolamine utilisation - propanediol utilisation | ||
BCJHNJMD_01202 | 9.5e-132 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
BCJHNJMD_01203 | 4.8e-207 | K | helix_turn_helix, arabinose operon control protein | |||
BCJHNJMD_01204 | 5.2e-41 | pduA_4 | CQ | BMC | ||
BCJHNJMD_01205 | 1.2e-129 | pduB | E | BMC | ||
BCJHNJMD_01206 | 0.0 | pduC | 4.2.1.28 | Q | Dehydratase large subunit | |
BCJHNJMD_01207 | 1e-128 | pduD | 4.2.1.28, 4.2.1.30 | Q | Dehydratase medium subunit | |
BCJHNJMD_01208 | 3e-90 | pduE | 4.2.1.28 | Q | Dehydratase small subunit | |
BCJHNJMD_01209 | 0.0 | pduG | D | Diol dehydratase reactivase ATPase-like domain | ||
BCJHNJMD_01210 | 1.1e-56 | pduH | S | Dehydratase medium subunit | ||
BCJHNJMD_01211 | 9.7e-83 | pduK | CQ | BMC | ||
BCJHNJMD_01212 | 4.9e-42 | pduA_4 | CQ | BMC | ||
BCJHNJMD_01213 | 6.1e-114 | pduL | 2.3.1.222, 2.3.1.8 | Q | Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate | |
BCJHNJMD_01214 | 3e-90 | S | Putative propanediol utilisation | |||
BCJHNJMD_01215 | 6e-42 | ccmL | CQ | Ethanolamine utilisation protein EutN/carboxysome | ||
BCJHNJMD_01216 | 5.8e-103 | pduO | 2.5.1.17 | S | Cobalamin adenosyltransferase | |
BCJHNJMD_01217 | 1.4e-81 | pduO | S | Haem-degrading | ||
BCJHNJMD_01218 | 1.6e-266 | pduP | 1.2.1.87 | C | Aldehyde dehydrogenase family | |
BCJHNJMD_01219 | 6.2e-210 | pduQ | C | Iron-containing alcohol dehydrogenase | ||
BCJHNJMD_01220 | 7e-220 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BCJHNJMD_01221 | 7.8e-55 | pduU | E | BMC | ||
BCJHNJMD_01222 | 3.5e-194 | C | Oxidoreductase | |||
BCJHNJMD_01223 | 1.1e-144 | 3.1.3.48 | T | Pfam:Y_phosphatase3C | ||
BCJHNJMD_01224 | 2.7e-58 | K | Helix-turn-helix XRE-family like proteins | |||
BCJHNJMD_01225 | 5.1e-37 | cro | K | Helix-turn-helix XRE-family like proteins | ||
BCJHNJMD_01226 | 1.3e-120 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
BCJHNJMD_01227 | 1.1e-233 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
BCJHNJMD_01228 | 1.1e-127 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
BCJHNJMD_01229 | 1.2e-172 | deoR | K | sugar-binding domain protein | ||
BCJHNJMD_01230 | 8.7e-240 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
BCJHNJMD_01231 | 1.4e-294 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
BCJHNJMD_01232 | 2.5e-65 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
BCJHNJMD_01233 | 4.1e-248 | fucP | G | Major Facilitator Superfamily | ||
BCJHNJMD_01234 | 1.8e-232 | potE | E | amino acid | ||
BCJHNJMD_01235 | 4.3e-213 | gntP | EG | Gluconate | ||
BCJHNJMD_01236 | 2.3e-303 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
BCJHNJMD_01237 | 3.2e-150 | gntR | K | rpiR family | ||
BCJHNJMD_01238 | 1.6e-145 | lys | M | Glycosyl hydrolases family 25 | ||
BCJHNJMD_01239 | 5.7e-64 | S | Domain of unknown function (DUF4828) | |||
BCJHNJMD_01240 | 7.3e-186 | mocA | S | Oxidoreductase | ||
BCJHNJMD_01241 | 7.6e-207 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
BCJHNJMD_01243 | 5.6e-77 | T | Universal stress protein family | |||
BCJHNJMD_01244 | 4.1e-232 | gntP | EG | Gluconate | ||
BCJHNJMD_01245 | 4.2e-159 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
BCJHNJMD_01246 | 6.7e-212 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
BCJHNJMD_01247 | 2.1e-157 | S | Nuclease-related domain | |||
BCJHNJMD_01248 | 9e-159 | yihY | S | Belongs to the UPF0761 family | ||
BCJHNJMD_01249 | 1e-78 | fld | C | Flavodoxin | ||
BCJHNJMD_01250 | 1.2e-143 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
BCJHNJMD_01251 | 2.3e-215 | pbpX2 | V | Beta-lactamase | ||
BCJHNJMD_01252 | 5.6e-39 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
BCJHNJMD_01253 | 4.4e-108 | ygaC | J | Belongs to the UPF0374 family | ||
BCJHNJMD_01254 | 1.4e-180 | yueF | S | AI-2E family transporter | ||
BCJHNJMD_01255 | 2.6e-76 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
BCJHNJMD_01256 | 2.9e-154 | |||||
BCJHNJMD_01257 | 0.0 | 2.7.8.12 | M | glycerophosphotransferase | ||
BCJHNJMD_01258 | 4.3e-87 | |||||
BCJHNJMD_01259 | 1.3e-306 | 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 | ||
BCJHNJMD_01260 | 4.5e-270 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BCJHNJMD_01261 | 1.8e-256 | nox | 1.6.3.4 | C | NADH oxidase | |
BCJHNJMD_01262 | 6.6e-281 | pipD | E | Dipeptidase | ||
BCJHNJMD_01263 | 0.0 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
BCJHNJMD_01264 | 1.7e-204 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
BCJHNJMD_01265 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
BCJHNJMD_01266 | 3.9e-30 | |||||
BCJHNJMD_01267 | 7.2e-40 | ptsH | G | phosphocarrier protein HPR | ||
BCJHNJMD_01268 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
BCJHNJMD_01269 | 2.7e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
BCJHNJMD_01270 | 1.7e-193 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
BCJHNJMD_01271 | 4.1e-184 | 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 | ||
BCJHNJMD_01272 | 4.3e-36 | ykuJ | S | Protein of unknown function (DUF1797) | ||
BCJHNJMD_01273 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
BCJHNJMD_01274 | 2.2e-120 | polC | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | S | WXG100 protein secretion system (Wss), protein YukC |
BCJHNJMD_01275 | 1.2e-184 | M | CHAP domain | |||
BCJHNJMD_01276 | 6.7e-81 | |||||
BCJHNJMD_01277 | 8.1e-58 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
BCJHNJMD_01278 | 7.6e-77 | |||||
BCJHNJMD_01279 | 1.2e-261 | traK | U | COG3505 Type IV secretory pathway, VirD4 components | ||
BCJHNJMD_01280 | 2e-147 | |||||
BCJHNJMD_01282 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
BCJHNJMD_01283 | 3.4e-25 | |||||
BCJHNJMD_01284 | 7.7e-59 | |||||
BCJHNJMD_01285 | 3.3e-47 | |||||
BCJHNJMD_01286 | 6.1e-225 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
BCJHNJMD_01289 | 1.3e-196 | |||||
BCJHNJMD_01290 | 1.3e-258 | bcsA | 2.4.1.12 | GT2 | M | PilZ domain |
BCJHNJMD_01291 | 2.1e-111 | 2.4.1.83 | GT2 | M | GtrA-like protein | |
BCJHNJMD_01292 | 8.2e-84 | L | Resolvase, N terminal domain | |||
BCJHNJMD_01293 | 2.3e-137 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
BCJHNJMD_01294 | 3.2e-29 | |||||
BCJHNJMD_01295 | 1.9e-41 | |||||
BCJHNJMD_01296 | 2.7e-23 | |||||
BCJHNJMD_01297 | 4.6e-132 | S | Fic/DOC family | |||
BCJHNJMD_01299 | 4.2e-38 | |||||
BCJHNJMD_01300 | 3.4e-24 | |||||
BCJHNJMD_01301 | 0.0 | traA | L | MobA MobL family protein | ||
BCJHNJMD_01302 | 9.6e-36 | |||||
BCJHNJMD_01303 | 2e-93 | |||||
BCJHNJMD_01304 | 1.1e-50 | S | Cag pathogenicity island, type IV secretory system | |||
BCJHNJMD_01305 | 2.5e-35 | |||||
BCJHNJMD_01306 | 1.1e-113 | |||||
BCJHNJMD_01307 | 0.0 | traE | U | type IV secretory pathway VirB4 | ||
BCJHNJMD_01308 | 6.4e-227 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
BCJHNJMD_01309 | 1.5e-100 | ahpC | 1.11.1.15 | O | Peroxiredoxin | |
BCJHNJMD_01310 | 7.2e-56 | |||||
BCJHNJMD_01311 | 4.6e-109 | ylbE | GM | NAD(P)H-binding | ||
BCJHNJMD_01312 | 3.7e-44 | |||||
BCJHNJMD_01313 | 2.7e-69 | K | Helix-turn-helix XRE-family like proteins | |||
BCJHNJMD_01316 | 1.9e-275 | 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 | |
BCJHNJMD_01317 | 4.8e-70 | K | Transcriptional regulator | |||
BCJHNJMD_01318 | 7e-43 | elaA | S | Gnat family | ||
BCJHNJMD_01319 | 4.5e-22 | |||||
BCJHNJMD_01320 | 2.3e-289 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
BCJHNJMD_01321 | 5.5e-155 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
BCJHNJMD_01322 | 7.4e-66 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_01323 | 7.9e-202 | calB | 1.2.1.68 | C | Belongs to the aldehyde dehydrogenase family | |
BCJHNJMD_01324 | 6.4e-159 | 1.1.1.65 | C | Aldo keto reductase | ||
BCJHNJMD_01325 | 1.2e-88 | |||||
BCJHNJMD_01326 | 2.3e-215 | yttB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_01327 | 7.1e-245 | glpT | G | Major Facilitator Superfamily | ||
BCJHNJMD_01328 | 7e-38 | ywnB | S | NAD(P)H-binding | ||
BCJHNJMD_01329 | 3.8e-90 | emrY | EGP | Major facilitator Superfamily | ||
BCJHNJMD_01330 | 2e-27 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_01331 | 4.7e-129 | nfrA | 1.5.1.39 | C | nitroreductase | |
BCJHNJMD_01332 | 4.5e-85 | nrdI | F | Belongs to the NrdI family | ||
BCJHNJMD_01333 | 2.1e-253 | S | ATPases associated with a variety of cellular activities | |||
BCJHNJMD_01334 | 1.7e-249 | lmrB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_01336 | 7.7e-143 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
BCJHNJMD_01337 | 5.2e-173 | K | Transcriptional regulator, LacI family | |||
BCJHNJMD_01338 | 7.6e-52 | K | transcriptional regulator | |||
BCJHNJMD_01339 | 1.8e-105 | yneD | S | Enoyl-(Acyl carrier protein) reductase | ||
BCJHNJMD_01340 | 3.3e-242 | yhdP | S | Transporter associated domain | ||
BCJHNJMD_01341 | 7.6e-61 | |||||
BCJHNJMD_01342 | 3.5e-73 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
BCJHNJMD_01343 | 5.8e-256 | yjeM | E | Amino Acid | ||
BCJHNJMD_01344 | 3.6e-162 | ytbE | 1.1.1.346 | S | Aldo keto reductase | |
BCJHNJMD_01346 | 0.0 | yfgQ | P | E1-E2 ATPase | ||
BCJHNJMD_01347 | 2.2e-93 | M1-874 | K | Domain of unknown function (DUF1836) | ||
BCJHNJMD_01348 | 0.0 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
BCJHNJMD_01349 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
BCJHNJMD_01350 | 5.9e-47 | M | LysM domain protein | |||
BCJHNJMD_01351 | 0.0 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | M | Leucine-rich repeat (LRR) protein | |
BCJHNJMD_01352 | 6e-56 | M | LysM domain protein | |||
BCJHNJMD_01354 | 6.5e-57 | M | LysM domain | |||
BCJHNJMD_01355 | 4.1e-161 | yteR | 3.2.1.172 | GH105 | S | Glycosyl Hydrolase Family 88 |
BCJHNJMD_01356 | 5.6e-246 | melB1_1 | G | MFS/sugar transport protein | ||
BCJHNJMD_01357 | 1.8e-92 | G | Xylose isomerase-like TIM barrel | |||
BCJHNJMD_01358 | 1.6e-148 | picA | 3.2.1.67 | G | Glycosyl hydrolases family 28 | |
BCJHNJMD_01360 | 2.3e-93 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_01361 | 1.9e-166 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
BCJHNJMD_01362 | 7.2e-178 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BCJHNJMD_01363 | 1.5e-217 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BCJHNJMD_01364 | 3.6e-53 | DR0488 | S | 3D domain | ||
BCJHNJMD_01365 | 1.9e-284 | M | Exporter of polyketide antibiotics | |||
BCJHNJMD_01366 | 4.2e-169 | yjjC | V | ABC transporter | ||
BCJHNJMD_01367 | 5.6e-118 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BCJHNJMD_01368 | 5.2e-248 | V | Polysaccharide biosynthesis C-terminal domain | |||
BCJHNJMD_01369 | 7e-283 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
BCJHNJMD_01370 | 1.4e-259 | gph | G | MFS/sugar transport protein | ||
BCJHNJMD_01371 | 0.0 | yicI | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
BCJHNJMD_01372 | 0.0 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
BCJHNJMD_01373 | 0.0 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
BCJHNJMD_01374 | 8.7e-167 | yqhA | G | Aldose 1-epimerase | ||
BCJHNJMD_01375 | 6e-120 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
BCJHNJMD_01376 | 5.9e-188 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |||
BCJHNJMD_01377 | 1.3e-303 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
BCJHNJMD_01378 | 5.1e-170 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
BCJHNJMD_01379 | 3.1e-127 | kdgR | K | FCD domain | ||
BCJHNJMD_01380 | 1.6e-207 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
BCJHNJMD_01381 | 2.4e-184 | exuR | K | Periplasmic binding protein domain | ||
BCJHNJMD_01382 | 1.8e-278 | yjmB | G | MFS/sugar transport protein | ||
BCJHNJMD_01383 | 4.8e-309 | 5.1.2.7 | S | tagaturonate epimerase | ||
BCJHNJMD_01384 | 4e-294 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
BCJHNJMD_01385 | 6.2e-227 | S | module of peptide synthetase | |||
BCJHNJMD_01387 | 9.6e-253 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_01388 | 6.2e-19 | S | Protein of unknown function (DUF3278) | |||
BCJHNJMD_01389 | 2.2e-19 | K | Helix-turn-helix XRE-family like proteins | |||
BCJHNJMD_01390 | 2.2e-64 | S | Leucine-rich repeat (LRR) protein | |||
BCJHNJMD_01391 | 8e-127 | |||||
BCJHNJMD_01392 | 3.2e-89 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
BCJHNJMD_01393 | 4.4e-132 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
BCJHNJMD_01394 | 2e-107 | O | Zinc-dependent metalloprotease | |||
BCJHNJMD_01395 | 1.2e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
BCJHNJMD_01396 | 5.1e-72 | |||||
BCJHNJMD_01397 | 2.6e-135 | plnC | K | LytTr DNA-binding domain | ||
BCJHNJMD_01398 | 1.6e-212 | 2.7.13.3 | T | GHKL domain | ||
BCJHNJMD_01399 | 7.5e-210 | 2.1.1.80, 2.7.13.3, 3.1.1.61 | T | protein histidine kinase activity | ||
BCJHNJMD_01400 | 8.8e-128 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
BCJHNJMD_01402 | 5.1e-167 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BCJHNJMD_01403 | 2.8e-76 | uspA | T | universal stress protein | ||
BCJHNJMD_01404 | 1.7e-95 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
BCJHNJMD_01405 | 1.4e-17 | |||||
BCJHNJMD_01407 | 1.5e-88 | 3.2.1.17 | M | hydrolase, family 25 | ||
BCJHNJMD_01408 | 5.6e-42 | |||||
BCJHNJMD_01410 | 6.2e-49 | D | nuclear chromosome segregation | |||
BCJHNJMD_01412 | 6.7e-181 | Z012_12235 | S | Baseplate J-like protein | ||
BCJHNJMD_01414 | 3.7e-43 | |||||
BCJHNJMD_01415 | 3e-133 | |||||
BCJHNJMD_01416 | 1.2e-15 | |||||
BCJHNJMD_01417 | 2.3e-61 | M | LysM domain | |||
BCJHNJMD_01418 | 9.8e-146 | M | Membrane | |||
BCJHNJMD_01422 | 7.1e-09 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
BCJHNJMD_01426 | 1.8e-59 | |||||
BCJHNJMD_01428 | 2.4e-179 | gpG | ||||
BCJHNJMD_01429 | 1.1e-41 | S | Domain of unknown function (DUF4355) | |||
BCJHNJMD_01430 | 8.8e-77 | S | Phage Mu protein F like protein | |||
BCJHNJMD_01431 | 3.8e-262 | S | Phage portal protein, SPP1 Gp6-like | |||
BCJHNJMD_01433 | 3.8e-158 | ps334 | S | Terminase-like family | ||
BCJHNJMD_01434 | 2.7e-71 | L | Terminase small subunit | |||
BCJHNJMD_01436 | 3.5e-12 | |||||
BCJHNJMD_01437 | 2.2e-25 | S | Protein of unknown function (DUF2829) | |||
BCJHNJMD_01438 | 2.8e-36 | |||||
BCJHNJMD_01440 | 4e-33 | 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 | |
BCJHNJMD_01441 | 1.5e-75 | |||||
BCJHNJMD_01443 | 1.3e-44 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
BCJHNJMD_01445 | 2.2e-23 | |||||
BCJHNJMD_01448 | 5.6e-13 | |||||
BCJHNJMD_01449 | 7.7e-102 | S | Putative HNHc nuclease | |||
BCJHNJMD_01450 | 4.7e-70 | |||||
BCJHNJMD_01451 | 2e-225 | dnaB | 3.6.4.12 | L | DnaB-like helicase C terminal domain | |
BCJHNJMD_01452 | 2.5e-114 | L | Helix-turn-helix domain | |||
BCJHNJMD_01453 | 1.7e-102 | S | Protein of unknown function (DUF669) | |||
BCJHNJMD_01454 | 2.2e-120 | S | AAA domain | |||
BCJHNJMD_01455 | 4.9e-141 | S | Protein of unknown function (DUF1351) | |||
BCJHNJMD_01462 | 4e-12 | |||||
BCJHNJMD_01463 | 4.6e-24 | K | ParB-like nuclease domain | |||
BCJHNJMD_01464 | 1.8e-33 | S | Protein of unknown function (DUF3102) | |||
BCJHNJMD_01469 | 1.3e-52 | K | COG3617 Prophage antirepressor | |||
BCJHNJMD_01470 | 1.7e-11 | ps115 | K | Cro/C1-type HTH DNA-binding domain | ||
BCJHNJMD_01472 | 4e-25 | |||||
BCJHNJMD_01473 | 4.5e-277 | L | Belongs to the 'phage' integrase family | |||
BCJHNJMD_01474 | 1.9e-122 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
BCJHNJMD_01475 | 1e-69 | 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 | |
BCJHNJMD_01476 | 4.2e-138 | yhfI | S | Metallo-beta-lactamase superfamily | ||
BCJHNJMD_01477 | 2.6e-91 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
BCJHNJMD_01478 | 8e-232 | N | Uncharacterized conserved protein (DUF2075) | |||
BCJHNJMD_01486 | 1.4e-184 | M | Glycosyl hydrolases family 25 | |||
BCJHNJMD_01494 | 1.6e-67 | S | Endodeoxyribonuclease RusA | |||
BCJHNJMD_01496 | 4e-33 | 3.1.3.16 | L | DnaD domain protein | ||
BCJHNJMD_01497 | 2.7e-109 | S | Phage portal protein, SPP1 Gp6-like | |||
BCJHNJMD_01498 | 2.3e-32 | S | head morphogenesis protein, SPP1 gp7 family | |||
BCJHNJMD_01499 | 9.4e-09 | S | Domain of unknown function (DUF4355) | |||
BCJHNJMD_01500 | 7.1e-99 | gpG | ||||
BCJHNJMD_01502 | 1.3e-41 | |||||
BCJHNJMD_01505 | 1.4e-07 | S | Protein of unknown function (DUF3383) | |||
BCJHNJMD_01506 | 2.1e-10 | |||||
BCJHNJMD_01510 | 4.7e-135 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
BCJHNJMD_01511 | 7e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
BCJHNJMD_01512 | 1.9e-124 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
BCJHNJMD_01513 | 3.1e-92 | MA20_25245 | K | FR47-like protein | ||
BCJHNJMD_01514 | 1.2e-140 | 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 |
BCJHNJMD_01515 | 4.1e-286 | 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 | |
BCJHNJMD_01516 | 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 | |
BCJHNJMD_01517 | 6.8e-72 | |||||
BCJHNJMD_01518 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
BCJHNJMD_01519 | 4e-89 | ydcK | S | Belongs to the SprT family | ||
BCJHNJMD_01520 | 3.7e-157 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
BCJHNJMD_01522 | 3.6e-150 | 4.1.1.52 | S | Amidohydrolase | ||
BCJHNJMD_01523 | 1.9e-123 | S | Alpha/beta hydrolase family | |||
BCJHNJMD_01524 | 1.4e-61 | yobS | K | transcriptional regulator | ||
BCJHNJMD_01525 | 1.6e-100 | S | Psort location CytoplasmicMembrane, score | |||
BCJHNJMD_01526 | 6.6e-75 | K | MarR family | |||
BCJHNJMD_01527 | 2.6e-245 | dinF | V | MatE | ||
BCJHNJMD_01528 | 5.8e-109 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
BCJHNJMD_01529 | 4.3e-55 | manL | 2.7.1.191 | G | PTS system fructose IIA component | |
BCJHNJMD_01530 | 1.4e-60 | pts10B | 2.7.1.191, 2.7.1.202 | G | PTS system sorbose subfamily IIB component | |
BCJHNJMD_01531 | 1.6e-116 | manM | G | PTS system | ||
BCJHNJMD_01532 | 1.8e-153 | manN | G | system, mannose fructose sorbose family IID component | ||
BCJHNJMD_01533 | 5.5e-176 | K | AI-2E family transporter | |||
BCJHNJMD_01534 | 2e-163 | 2.7.7.65 | T | diguanylate cyclase | ||
BCJHNJMD_01535 | 1.4e-116 | yliE | T | EAL domain | ||
BCJHNJMD_01536 | 2.7e-100 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_01537 | 3.8e-208 | XK27_06930 | V | domain protein | ||
BCJHNJMD_01538 | 5.7e-169 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
BCJHNJMD_01539 | 4.6e-205 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BCJHNJMD_01540 | 6.1e-166 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
BCJHNJMD_01541 | 3.4e-170 | EG | EamA-like transporter family | |||
BCJHNJMD_01542 | 4.2e-121 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
BCJHNJMD_01543 | 4e-226 | V | Beta-lactamase | |||
BCJHNJMD_01544 | 5e-259 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
BCJHNJMD_01546 | 5.3e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
BCJHNJMD_01547 | 7.8e-55 | |||||
BCJHNJMD_01548 | 7.3e-100 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
BCJHNJMD_01549 | 4.1e-256 | 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 | ||
BCJHNJMD_01550 | 4.9e-213 | yacL | S | domain protein | ||
BCJHNJMD_01551 | 3.1e-289 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
BCJHNJMD_01552 | 1.7e-276 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BCJHNJMD_01553 | 7.8e-70 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
BCJHNJMD_01554 | 5.7e-138 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BCJHNJMD_01555 | 6.3e-91 | yacP | S | YacP-like NYN domain | ||
BCJHNJMD_01556 | 9.1e-78 | sigH | K | Sigma-70 region 2 | ||
BCJHNJMD_01557 | 4.3e-25 | 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 | ||
BCJHNJMD_01558 | 1.1e-98 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
BCJHNJMD_01559 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
BCJHNJMD_01560 | 1.2e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
BCJHNJMD_01561 | 7.7e-83 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
BCJHNJMD_01562 | 4e-49 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
BCJHNJMD_01563 | 0.0 | mprF | 2.3.2.3 | 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 | |
BCJHNJMD_01564 | 9.6e-106 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
BCJHNJMD_01565 | 2.6e-166 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
BCJHNJMD_01566 | 8.5e-195 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BCJHNJMD_01567 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
BCJHNJMD_01568 | 4.9e-37 | nrdH | O | Glutaredoxin | ||
BCJHNJMD_01569 | 5.2e-110 | rsmC | 2.1.1.172 | J | Methyltransferase | |
BCJHNJMD_01570 | 6e-89 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
BCJHNJMD_01571 | 1.7e-299 | 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 | |
BCJHNJMD_01572 | 1.6e-38 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
BCJHNJMD_01573 | 1.1e-109 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
BCJHNJMD_01574 | 1.3e-38 | yaaL | S | Protein of unknown function (DUF2508) | ||
BCJHNJMD_01575 | 5.1e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
BCJHNJMD_01576 | 2.2e-54 | yaaQ | S | Cyclic-di-AMP receptor | ||
BCJHNJMD_01577 | 6.7e-179 | holB | 2.7.7.7 | L | DNA polymerase III | |
BCJHNJMD_01578 | 1.7e-38 | yabA | L | Involved in initiation control of chromosome replication | ||
BCJHNJMD_01579 | 2.6e-163 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
BCJHNJMD_01580 | 4e-141 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
BCJHNJMD_01581 | 3.2e-127 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
BCJHNJMD_01582 | 9.8e-109 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
BCJHNJMD_01583 | 1.4e-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 | |
BCJHNJMD_01584 | 5.7e-214 | yeaN | P | Transporter, major facilitator family protein | ||
BCJHNJMD_01585 | 7.5e-46 | cadC1 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
BCJHNJMD_01586 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
BCJHNJMD_01587 | 6.9e-113 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
BCJHNJMD_01588 | 3e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
BCJHNJMD_01589 | 6.5e-293 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
BCJHNJMD_01590 | 0.0 | ydaO | E | amino acid | ||
BCJHNJMD_01591 | 3.7e-140 | lrgB | M | LrgB-like family | ||
BCJHNJMD_01592 | 1.6e-60 | lrgA | S | LrgA family | ||
BCJHNJMD_01593 | 3.6e-178 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
BCJHNJMD_01594 | 1.3e-114 | yvyE | 3.4.13.9 | S | YigZ family | |
BCJHNJMD_01595 | 8.2e-254 | comFA | L | Helicase C-terminal domain protein | ||
BCJHNJMD_01596 | 2e-123 | comFC | S | Competence protein | ||
BCJHNJMD_01597 | 7.9e-97 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
BCJHNJMD_01598 | 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 | ||
BCJHNJMD_01599 | 5.6e-186 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
BCJHNJMD_01600 | 4.3e-222 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
BCJHNJMD_01601 | 7.6e-129 | K | response regulator | |||
BCJHNJMD_01602 | 3.1e-248 | phoR | 2.7.13.3 | T | Histidine kinase | |
BCJHNJMD_01603 | 2.1e-160 | pstS | P | Phosphate | ||
BCJHNJMD_01604 | 2e-158 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
BCJHNJMD_01605 | 7.7e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
BCJHNJMD_01606 | 1.8e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
BCJHNJMD_01607 | 3.5e-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 | |
BCJHNJMD_01608 | 1.4e-119 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
BCJHNJMD_01609 | 1.7e-54 | pspC | KT | PspC domain protein | ||
BCJHNJMD_01610 | 5.5e-30 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
BCJHNJMD_01611 | 9.5e-172 | 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 | ||
BCJHNJMD_01612 | 7.3e-150 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
BCJHNJMD_01613 | 7.6e-183 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
BCJHNJMD_01614 | 2.8e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
BCJHNJMD_01615 | 4.5e-177 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
BCJHNJMD_01617 | 1.9e-115 | yfbR | S | HD containing hydrolase-like enzyme | ||
BCJHNJMD_01618 | 4.5e-94 | K | acetyltransferase | |||
BCJHNJMD_01619 | 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 | ||
BCJHNJMD_01620 | 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 | ||
BCJHNJMD_01621 | 2.4e-90 | S | Short repeat of unknown function (DUF308) | |||
BCJHNJMD_01622 | 4.8e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
BCJHNJMD_01623 | 3.4e-191 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
BCJHNJMD_01624 | 9.9e-169 | whiA | K | May be required for sporulation | ||
BCJHNJMD_01625 | 1.7e-102 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
BCJHNJMD_01626 | 2.8e-73 | XK27_02470 | K | LytTr DNA-binding domain | ||
BCJHNJMD_01627 | 3.9e-125 | liaI | S | membrane | ||
BCJHNJMD_01629 | 1.4e-107 | S | ECF transporter, substrate-specific component | |||
BCJHNJMD_01631 | 1e-182 | cggR | K | Putative sugar-binding domain | ||
BCJHNJMD_01632 | 9e-192 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
BCJHNJMD_01633 | 4.3e-225 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
BCJHNJMD_01634 | 2.3e-139 | 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) | |
BCJHNJMD_01635 | 8e-249 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
BCJHNJMD_01637 | 7.6e-283 | clcA | P | chloride | ||
BCJHNJMD_01638 | 4.9e-32 | secG | U | Preprotein translocase | ||
BCJHNJMD_01639 | 8.1e-137 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
BCJHNJMD_01640 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
BCJHNJMD_01641 | 2.3e-81 | 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 | ||
BCJHNJMD_01642 | 7.6e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BCJHNJMD_01643 | 4.9e-102 | yxjI | ||||
BCJHNJMD_01644 | 3e-141 | 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 | |
BCJHNJMD_01645 | 1.6e-177 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
BCJHNJMD_01646 | 1.9e-83 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
BCJHNJMD_01647 | 1.4e-87 | 2.3.1.128, 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
BCJHNJMD_01648 | 2.8e-193 | C | Aldo keto reductase family protein | |||
BCJHNJMD_01649 | 6e-102 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
BCJHNJMD_01650 | 1.3e-150 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
BCJHNJMD_01651 | 5e-165 | murB | 1.3.1.98 | M | Cell wall formation | |
BCJHNJMD_01652 | 0.0 | yjcE | P | Sodium proton antiporter | ||
BCJHNJMD_01653 | 1.7e-122 | S | Protein of unknown function (DUF1361) | |||
BCJHNJMD_01654 | 1e-151 | 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 | |
BCJHNJMD_01655 | 1.5e-132 | ybbR | S | YbbR-like protein | ||
BCJHNJMD_01656 | 7.2e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
BCJHNJMD_01657 | 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 | |
BCJHNJMD_01658 | 1.7e-12 | |||||
BCJHNJMD_01659 | 2.7e-129 | 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 | |
BCJHNJMD_01660 | 1.3e-252 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
BCJHNJMD_01661 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
BCJHNJMD_01662 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
BCJHNJMD_01663 | 2.8e-94 | dps | P | Belongs to the Dps family | ||
BCJHNJMD_01664 | 1.1e-25 | copZ | P | Heavy-metal-associated domain | ||
BCJHNJMD_01665 | 1.9e-200 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
BCJHNJMD_01666 | 6.2e-51 | |||||
BCJHNJMD_01667 | 8.3e-78 | S | Iron Transport-associated domain | |||
BCJHNJMD_01668 | 2.1e-163 | M | Iron Transport-associated domain | |||
BCJHNJMD_01669 | 2.2e-89 | M | Iron Transport-associated domain | |||
BCJHNJMD_01670 | 9.5e-161 | isdE | P | Periplasmic binding protein | ||
BCJHNJMD_01671 | 2.9e-171 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
BCJHNJMD_01672 | 6.2e-137 | fhuC | 3.6.3.34 | HP | ABC transporter, ATP-binding protein | |
BCJHNJMD_01673 | 5.8e-169 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BCJHNJMD_01674 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
BCJHNJMD_01675 | 7e-289 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BCJHNJMD_01676 | 5.3e-150 | licD | M | LicD family | ||
BCJHNJMD_01677 | 1.7e-75 | S | Domain of unknown function (DUF5067) | |||
BCJHNJMD_01678 | 2.3e-75 | K | Transcriptional regulator | |||
BCJHNJMD_01679 | 1.9e-25 | |||||
BCJHNJMD_01680 | 1.3e-78 | O | OsmC-like protein | |||
BCJHNJMD_01681 | 8.3e-24 | |||||
BCJHNJMD_01683 | 3.8e-55 | ypaA | S | Protein of unknown function (DUF1304) | ||
BCJHNJMD_01684 | 2.9e-87 | |||||
BCJHNJMD_01685 | 1.2e-255 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
BCJHNJMD_01686 | 3.5e-45 | sigM | K | Sigma-70 region 2 | ||
BCJHNJMD_01687 | 1.7e-72 | S | Sigma factor regulator C-terminal | |||
BCJHNJMD_01688 | 5e-254 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
BCJHNJMD_01689 | 3.8e-209 | G | MFS/sugar transport protein | |||
BCJHNJMD_01690 | 6.6e-120 | K | AraC family transcriptional regulator | |||
BCJHNJMD_01691 | 0.0 | rafA | 3.2.1.22 | G | Melibiase | |
BCJHNJMD_01694 | 9e-147 | K | response regulator | |||
BCJHNJMD_01695 | 5.5e-267 | T | PhoQ Sensor | |||
BCJHNJMD_01696 | 4.9e-210 | ywbD | 2.1.1.191 | J | S-adenosylmethionine-dependent methyltransferase | |
BCJHNJMD_01697 | 6.4e-154 | glcU | U | sugar transport | ||
BCJHNJMD_01698 | 7.1e-261 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
BCJHNJMD_01699 | 0.0 | S | Bacterial membrane protein YfhO | |||
BCJHNJMD_01700 | 5.2e-81 | tspO | T | TspO/MBR family | ||
BCJHNJMD_01701 | 3.8e-99 | S | Protein of unknown function (DUF1211) | |||
BCJHNJMD_01704 | 9.9e-164 | S | NAD:arginine ADP-ribosyltransferase | |||
BCJHNJMD_01705 | 1.6e-197 | ybiR | P | Citrate transporter | ||
BCJHNJMD_01706 | 7.8e-120 | yliE | T | Putative diguanylate phosphodiesterase | ||
BCJHNJMD_01707 | 1.2e-147 | 2.7.7.65 | T | diguanylate cyclase | ||
BCJHNJMD_01708 | 8.7e-09 | |||||
BCJHNJMD_01709 | 8.9e-56 | |||||
BCJHNJMD_01710 | 0.0 | lmrA | V | ABC transporter, ATP-binding protein | ||
BCJHNJMD_01711 | 0.0 | yfiC | V | ABC transporter | ||
BCJHNJMD_01712 | 4.3e-194 | ampC | V | Beta-lactamase | ||
BCJHNJMD_01713 | 1.3e-133 | cobQ | S | glutamine amidotransferase | ||
BCJHNJMD_01714 | 1.2e-263 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
BCJHNJMD_01715 | 8.5e-110 | tdk | 2.7.1.21 | F | thymidine kinase | |
BCJHNJMD_01716 | 7.9e-186 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
BCJHNJMD_01717 | 1.7e-151 | 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 | |
BCJHNJMD_01718 | 7.2e-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 | |
BCJHNJMD_01719 | 7.8e-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 | |
BCJHNJMD_01720 | 1.5e-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 | |
BCJHNJMD_01721 | 6.1e-126 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
BCJHNJMD_01722 | 7.3e-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 | ||
BCJHNJMD_01723 | 3.4e-54 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
BCJHNJMD_01724 | 2e-89 | 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 | ||
BCJHNJMD_01725 | 1.7e-287 | 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 | |
BCJHNJMD_01726 | 7.3e-161 | 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 | ||
BCJHNJMD_01727 | 5.3e-267 | 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 | |
BCJHNJMD_01728 | 1.1e-66 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
BCJHNJMD_01729 | 4.3e-33 | ywzB | S | Protein of unknown function (DUF1146) | ||
BCJHNJMD_01730 | 1.3e-243 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BCJHNJMD_01731 | 1.8e-179 | mbl | D | Cell shape determining protein MreB Mrl | ||
BCJHNJMD_01732 | 1.1e-52 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
BCJHNJMD_01733 | 1.1e-33 | S | Protein of unknown function (DUF2969) | |||
BCJHNJMD_01734 | 1.1e-220 | rodA | D | Belongs to the SEDS family | ||
BCJHNJMD_01735 | 1.9e-49 | gcsH2 | E | glycine cleavage | ||
BCJHNJMD_01736 | 3.9e-140 | f42a | O | Band 7 protein | ||
BCJHNJMD_01737 | 3e-176 | S | Protein of unknown function (DUF2785) | |||
BCJHNJMD_01738 | 1.2e-216 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
BCJHNJMD_01739 | 9e-300 | glpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
BCJHNJMD_01740 | 7.9e-160 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
BCJHNJMD_01741 | 1e-81 | usp6 | T | universal stress protein | ||
BCJHNJMD_01742 | 3.2e-41 | |||||
BCJHNJMD_01743 | 1.2e-236 | rarA | L | recombination factor protein RarA | ||
BCJHNJMD_01744 | 7.1e-80 | yueI | S | Protein of unknown function (DUF1694) | ||
BCJHNJMD_01745 | 1.3e-110 | yktB | S | Belongs to the UPF0637 family | ||
BCJHNJMD_01746 | 7.1e-61 | KLT | serine threonine protein kinase | |||
BCJHNJMD_01747 | 4.8e-108 | 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 | ||
BCJHNJMD_01748 | 2.4e-83 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
BCJHNJMD_01749 | 0.0 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
BCJHNJMD_01750 | 7.2e-214 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
BCJHNJMD_01751 | 1.9e-228 | 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 | |
BCJHNJMD_01752 | 3.5e-91 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
BCJHNJMD_01753 | 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 | |
BCJHNJMD_01754 | 1.8e-248 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
BCJHNJMD_01755 | 8.1e-117 | radC | L | DNA repair protein | ||
BCJHNJMD_01756 | 9.6e-162 | mreB | D | cell shape determining protein MreB | ||
BCJHNJMD_01757 | 9.7e-139 | mreC | M | Involved in formation and maintenance of cell shape | ||
BCJHNJMD_01758 | 3.2e-92 | mreD | M | rod shape-determining protein MreD | ||
BCJHNJMD_01759 | 8.2e-117 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
BCJHNJMD_01760 | 4.1e-147 | minD | D | Belongs to the ParA family | ||
BCJHNJMD_01761 | 2.5e-110 | glnP | P | ABC transporter permease | ||
BCJHNJMD_01762 | 4.2e-94 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BCJHNJMD_01763 | 1.4e-158 | aatB | ET | ABC transporter substrate-binding protein | ||
BCJHNJMD_01764 | 6.4e-235 | ymfF | S | Peptidase M16 inactive domain protein | ||
BCJHNJMD_01765 | 1.1e-245 | ymfH | S | Peptidase M16 | ||
BCJHNJMD_01766 | 2.6e-65 | ymfM | S | Domain of unknown function (DUF4115) | ||
BCJHNJMD_01767 | 1e-99 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
BCJHNJMD_01768 | 3.7e-227 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
BCJHNJMD_01769 | 6.8e-188 | 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 | ||
BCJHNJMD_01771 | 4e-223 | rny | S | Endoribonuclease that initiates mRNA decay | ||
BCJHNJMD_01772 | 5.1e-150 | ymdB | S | YmdB-like protein | ||
BCJHNJMD_01773 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
BCJHNJMD_01774 | 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 | ||
BCJHNJMD_01775 | 1.4e-107 | 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 | |
BCJHNJMD_01776 | 6.5e-190 | 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 | |
BCJHNJMD_01777 | 4.1e-200 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
BCJHNJMD_01778 | 3e-228 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
BCJHNJMD_01779 | 1.1e-26 | yajC | U | Preprotein translocase | ||
BCJHNJMD_01780 | 1.5e-179 | 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 | |
BCJHNJMD_01781 | 9e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
BCJHNJMD_01782 | 6.1e-252 | 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 | |
BCJHNJMD_01783 | 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 | |
BCJHNJMD_01784 | 6.4e-44 | yrzL | S | Belongs to the UPF0297 family | ||
BCJHNJMD_01785 | 1.5e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
BCJHNJMD_01786 | 1.6e-51 | yrzB | S | Belongs to the UPF0473 family | ||
BCJHNJMD_01787 | 7.3e-37 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
BCJHNJMD_01788 | 3.2e-87 | cvpA | S | Colicin V production protein | ||
BCJHNJMD_01789 | 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 | ||
BCJHNJMD_01790 | 2.7e-54 | trxA | O | Belongs to the thioredoxin family | ||
BCJHNJMD_01791 | 6.7e-90 | yslB | S | Protein of unknown function (DUF2507) | ||
BCJHNJMD_01792 | 4.7e-146 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
BCJHNJMD_01793 | 1.4e-107 | 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 | |
BCJHNJMD_01794 | 7.3e-97 | S | Phosphoesterase | |||
BCJHNJMD_01795 | 1.8e-84 | ykuL | S | (CBS) domain | ||
BCJHNJMD_01797 | 1.4e-47 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
BCJHNJMD_01798 | 8.9e-243 | U | Major Facilitator Superfamily | |||
BCJHNJMD_01800 | 4.1e-156 | ykuT | M | mechanosensitive ion channel | ||
BCJHNJMD_01801 | 6.9e-34 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
BCJHNJMD_01802 | 9.5e-43 | |||||
BCJHNJMD_01803 | 2.7e-210 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BCJHNJMD_01804 | 4.6e-180 | ccpA | K | catabolite control protein A | ||
BCJHNJMD_01805 | 5.7e-128 | |||||
BCJHNJMD_01806 | 8.2e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
BCJHNJMD_01807 | 6.2e-266 | glnPH2 | P | ABC transporter permease | ||
BCJHNJMD_01808 | 2.6e-132 | yebC | K | Transcriptional regulatory protein | ||
BCJHNJMD_01809 | 1.2e-172 | comGA | NU | Type II IV secretion system protein | ||
BCJHNJMD_01810 | 3.8e-168 | comGB | NU | type II secretion system | ||
BCJHNJMD_01811 | 7.6e-49 | comGC | U | competence protein ComGC | ||
BCJHNJMD_01812 | 1.2e-79 | |||||
BCJHNJMD_01814 | 7.1e-74 | |||||
BCJHNJMD_01815 | 1.1e-184 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
BCJHNJMD_01816 | 1.1e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
BCJHNJMD_01817 | 8.5e-257 | cycA | E | Amino acid permease | ||
BCJHNJMD_01818 | 6.2e-154 | yeaE | S | Aldo keto | ||
BCJHNJMD_01819 | 5.3e-115 | S | Calcineurin-like phosphoesterase | |||
BCJHNJMD_01820 | 3.6e-268 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
BCJHNJMD_01821 | 2.9e-82 | yutD | S | Protein of unknown function (DUF1027) | ||
BCJHNJMD_01822 | 1.3e-145 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
BCJHNJMD_01823 | 6.5e-116 | S | Protein of unknown function (DUF1461) | |||
BCJHNJMD_01824 | 7.7e-88 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_01825 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BCJHNJMD_01826 | 2e-234 | M | domain protein | |||
BCJHNJMD_01827 | 2.4e-251 | yfnA | E | Amino Acid | ||
BCJHNJMD_01828 | 4.8e-140 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
BCJHNJMD_01829 | 4.5e-112 | ytbE | C | Aldo keto reductase | ||
BCJHNJMD_01830 | 1.8e-63 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
BCJHNJMD_01831 | 3.4e-13 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_01832 | 2.9e-122 | dedA | S | SNARE-like domain protein | ||
BCJHNJMD_01833 | 6.1e-88 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
BCJHNJMD_01834 | 3.5e-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 | |
BCJHNJMD_01835 | 5.2e-71 | yugI | 5.3.1.9 | J | general stress protein | |
BCJHNJMD_01837 | 1.2e-07 | |||||
BCJHNJMD_01853 | 2.2e-08 | |||||
BCJHNJMD_01856 | 1e-81 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
BCJHNJMD_01857 | 7.7e-25 | KT | PspC domain | |||
BCJHNJMD_01858 | 1.2e-123 | G | phosphoglycerate mutase | |||
BCJHNJMD_01859 | 6.9e-164 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
BCJHNJMD_01860 | 8.7e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
BCJHNJMD_01861 | 2.1e-79 | |||||
BCJHNJMD_01862 | 9.3e-77 | F | nucleoside 2-deoxyribosyltransferase | |||
BCJHNJMD_01863 | 3.1e-110 | 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 | |
BCJHNJMD_01864 | 1.8e-37 | ynzC | S | UPF0291 protein | ||
BCJHNJMD_01865 | 1.6e-32 | yneF | S | Uncharacterised protein family (UPF0154) | ||
BCJHNJMD_01866 | 1.2e-287 | mdlA | V | ABC transporter | ||
BCJHNJMD_01867 | 0.0 | mdlB | V | ABC transporter | ||
BCJHNJMD_01868 | 7.6e-120 | plsC | 2.3.1.51 | I | Acyltransferase | |
BCJHNJMD_01869 | 3.3e-135 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
BCJHNJMD_01870 | 6.4e-44 | yazA | L | GIY-YIG catalytic domain protein | ||
BCJHNJMD_01871 | 1.5e-183 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
BCJHNJMD_01872 | 9.4e-135 | S | Haloacid dehalogenase-like hydrolase | |||
BCJHNJMD_01873 | 3.8e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
BCJHNJMD_01874 | 1.9e-153 | 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 | ||
BCJHNJMD_01875 | 5e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
BCJHNJMD_01876 | 6.9e-85 | 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 | ||
BCJHNJMD_01877 | 3.2e-74 | |||||
BCJHNJMD_01878 | 4e-147 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BCJHNJMD_01879 | 4.2e-136 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
BCJHNJMD_01880 | 5.6e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
BCJHNJMD_01881 | 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 | |
BCJHNJMD_01882 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BCJHNJMD_01883 | 7e-38 | |||||
BCJHNJMD_01884 | 1.8e-81 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
BCJHNJMD_01885 | 1.5e-190 | nusA | K | Participates in both transcription termination and antitermination | ||
BCJHNJMD_01886 | 2.3e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
BCJHNJMD_01887 | 1.4e-44 | ylxQ | J | ribosomal protein | ||
BCJHNJMD_01888 | 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 | ||
BCJHNJMD_01889 | 9.4e-56 | 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 | ||
BCJHNJMD_01890 | 6.9e-167 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
BCJHNJMD_01891 | 3.1e-178 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
BCJHNJMD_01892 | 7.8e-191 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
BCJHNJMD_01893 | 2.8e-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 | ||
BCJHNJMD_01894 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
BCJHNJMD_01895 | 4.9e-178 | 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 | ||
BCJHNJMD_01896 | 1.7e-17 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
BCJHNJMD_01897 | 2.9e-295 | 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 | |
BCJHNJMD_01898 | 3.8e-237 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
BCJHNJMD_01899 | 5.2e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
BCJHNJMD_01900 | 3.2e-250 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
BCJHNJMD_01901 | 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 | ||
BCJHNJMD_01902 | 1.1e-19 | asnB | 6.3.5.4 | E | Protein of unknown function (DUF3923) | |
BCJHNJMD_01904 | 1.1e-209 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
BCJHNJMD_01905 | 3.3e-42 | |||||
BCJHNJMD_01907 | 1.8e-62 | |||||
BCJHNJMD_01908 | 1.3e-26 | 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 | ||
BCJHNJMD_01909 | 1.2e-54 | |||||
BCJHNJMD_01910 | 3.1e-178 | prmA | J | Ribosomal protein L11 methyltransferase | ||
BCJHNJMD_01911 | 7e-133 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
BCJHNJMD_01912 | 1.8e-59 | |||||
BCJHNJMD_01913 | 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 | |
BCJHNJMD_01914 | 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 | ||
BCJHNJMD_01915 | 8.1e-114 | 3.1.3.18 | S | HAD-hyrolase-like | ||
BCJHNJMD_01916 | 1.5e-163 | yniA | G | Fructosamine kinase | ||
BCJHNJMD_01917 | 2.1e-157 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
BCJHNJMD_01918 | 2e-97 | |||||
BCJHNJMD_01919 | 1.5e-247 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
BCJHNJMD_01920 | 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) | |
BCJHNJMD_01921 | 1.8e-95 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
BCJHNJMD_01922 | 3.8e-162 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
BCJHNJMD_01923 | 8.5e-189 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
BCJHNJMD_01924 | 8e-151 | tagG | U | Transport permease protein | ||
BCJHNJMD_01925 | 1.1e-241 | tagF1 | 2.7.8.12, 2.7.8.45 | M | glycerophosphotransferase | |
BCJHNJMD_01926 | 1.2e-171 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
BCJHNJMD_01927 | 1.1e-150 | 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 | |
BCJHNJMD_01928 | 1.3e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
BCJHNJMD_01929 | 1.1e-189 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
BCJHNJMD_01930 | 9.1e-65 | hxlR | K | Transcriptional regulator, HxlR family | ||
BCJHNJMD_01931 | 7e-72 | yqeY | S | YqeY-like protein | ||
BCJHNJMD_01932 | 5.3e-181 | phoH | T | phosphate starvation-inducible protein PhoH | ||
BCJHNJMD_01933 | 8.5e-79 | 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 | |
BCJHNJMD_01934 | 3.4e-62 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
BCJHNJMD_01935 | 1.5e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
BCJHNJMD_01936 | 3.3e-149 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
BCJHNJMD_01937 | 1.5e-177 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
BCJHNJMD_01938 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
BCJHNJMD_01939 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
BCJHNJMD_01940 | 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 | ||
BCJHNJMD_01941 | 1.6e-88 | K | Transcriptional regulator | |||
BCJHNJMD_01942 | 0.0 | ydgH | S | MMPL family | ||
BCJHNJMD_01943 | 6.6e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
BCJHNJMD_01944 | 7.7e-154 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
BCJHNJMD_01945 | 2.5e-236 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
BCJHNJMD_01946 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
BCJHNJMD_01947 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
BCJHNJMD_01948 | 7.3e-127 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
BCJHNJMD_01949 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
BCJHNJMD_01950 | 6e-168 | cvfB | S | S1 domain | ||
BCJHNJMD_01951 | 8.3e-165 | xerD | D | recombinase XerD | ||
BCJHNJMD_01952 | 1.2e-70 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
BCJHNJMD_01953 | 2.4e-131 | 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 | ||
BCJHNJMD_01954 | 3e-102 | 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 | ||
BCJHNJMD_01955 | 2.7e-129 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
BCJHNJMD_01956 | 1.1e-93 | 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 | |||
BCJHNJMD_01957 | 4.3e-181 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
BCJHNJMD_01958 | 8.3e-252 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
BCJHNJMD_01959 | 8e-26 | M | Lysin motif | |||
BCJHNJMD_01960 | 6.4e-117 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
BCJHNJMD_01961 | 1.1e-210 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
BCJHNJMD_01962 | 9.7e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
BCJHNJMD_01963 | 1.5e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
BCJHNJMD_01964 | 1.2e-233 | S | Tetratricopeptide repeat protein | |||
BCJHNJMD_01965 | 1.3e-171 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
BCJHNJMD_01966 | 8.3e-221 | 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 | |
BCJHNJMD_01967 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
BCJHNJMD_01968 | 6.3e-187 | 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 | |
BCJHNJMD_01969 | 3.3e-91 | 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 | |
BCJHNJMD_01970 | 2.8e-114 | hlyIII | S | protein, hemolysin III | ||
BCJHNJMD_01971 | 1.4e-148 | DegV | S | EDD domain protein, DegV family | ||
BCJHNJMD_01972 | 3e-162 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
BCJHNJMD_01973 | 6.5e-105 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
BCJHNJMD_01974 | 5.8e-35 | yozE | S | Belongs to the UPF0346 family | ||
BCJHNJMD_01975 | 2.7e-239 | fucP | G | Major Facilitator Superfamily | ||
BCJHNJMD_01976 | 7.4e-178 | S | Domain of unknown function (DUF4432) | |||
BCJHNJMD_01977 | 4.8e-266 | 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
BCJHNJMD_01978 | 3.2e-135 | K | sugar-binding domain protein | |||
BCJHNJMD_01979 | 2.7e-115 | |||||
BCJHNJMD_01980 | 1e-48 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
BCJHNJMD_01982 | 5.5e-78 | S | AAA ATPase domain | |||
BCJHNJMD_01983 | 1.3e-34 | vrlR | S | Domain of unknown function (DUF1837) | ||
BCJHNJMD_01984 | 6.3e-108 | vrlS | L | helicase superfamily c-terminal domain | ||
BCJHNJMD_01985 | 6.1e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
BCJHNJMD_01986 | 1e-134 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
BCJHNJMD_01987 | 2.2e-165 | dprA | LU | DNA protecting protein DprA | ||
BCJHNJMD_01988 | 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 | |
BCJHNJMD_01989 | 5.8e-177 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
BCJHNJMD_01990 | 1.8e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
BCJHNJMD_01991 | 1.8e-262 | 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 | ||
BCJHNJMD_01992 | 1.2e-168 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
BCJHNJMD_01993 | 3.2e-99 | 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 | |
BCJHNJMD_01994 | 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 | |
BCJHNJMD_01995 | 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 | |
BCJHNJMD_01996 | 1.6e-182 | K | Transcriptional regulator | |||
BCJHNJMD_01997 | 8.3e-168 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
BCJHNJMD_01998 | 5.4e-101 | zmp1 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
BCJHNJMD_01999 | 1.3e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
BCJHNJMD_02000 | 1.4e-98 | 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 | |
BCJHNJMD_02001 | 3.6e-68 | 3.6.1.55 | F | NUDIX domain | ||
BCJHNJMD_02002 | 3.6e-199 | xerS | L | Belongs to the 'phage' integrase family | ||
BCJHNJMD_02003 | 6.4e-68 | ccpA | K | Psort location Cytoplasmic, score | ||
BCJHNJMD_02004 | 1.8e-211 | G | of the major facilitator superfamily | |||
BCJHNJMD_02005 | 2.8e-83 | G | Glycosyl hydrolases family 15 | |||
BCJHNJMD_02006 | 1.6e-65 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02007 | 1.1e-207 | S | membrane | |||
BCJHNJMD_02008 | 2.5e-43 | I | sulfurtransferase activity | |||
BCJHNJMD_02009 | 7.5e-59 | S | Phosphatidylethanolamine-binding protein | |||
BCJHNJMD_02010 | 1.2e-93 | GM | NAD(P)H-binding | |||
BCJHNJMD_02011 | 1.8e-120 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BCJHNJMD_02012 | 1.9e-140 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
BCJHNJMD_02013 | 1.4e-69 | K | Transcriptional regulator | |||
BCJHNJMD_02014 | 2.9e-75 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BCJHNJMD_02016 | 7.9e-121 | yneE | K | Transcriptional regulator | ||
BCJHNJMD_02017 | 5.6e-120 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BCJHNJMD_02018 | 2.9e-120 | Q | Methyltransferase domain | |||
BCJHNJMD_02019 | 1.8e-35 | yobS | K | transcriptional regulator | ||
BCJHNJMD_02020 | 4.7e-46 | S | Phosphatidylethanolamine-binding protein | |||
BCJHNJMD_02021 | 5.2e-72 | S | membrane transporter protein | |||
BCJHNJMD_02022 | 1.3e-67 | IQ | KR domain | |||
BCJHNJMD_02023 | 1.5e-20 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02024 | 9.9e-84 | C | Zinc-binding dehydrogenase | |||
BCJHNJMD_02025 | 6.9e-170 | C | Zinc-binding dehydrogenase | |||
BCJHNJMD_02026 | 1e-142 | mta | K | helix_turn_helix, mercury resistance | ||
BCJHNJMD_02027 | 2.5e-118 | 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 | |
BCJHNJMD_02028 | 2.2e-90 | V | VanZ like family | |||
BCJHNJMD_02029 | 3.5e-83 | ysaA | V | VanZ like family | ||
BCJHNJMD_02030 | 1.9e-74 | gtcA | S | Teichoic acid glycosylation protein | ||
BCJHNJMD_02031 | 4.1e-87 | folT | S | ECF transporter, substrate-specific component | ||
BCJHNJMD_02032 | 7.8e-160 | degV | S | EDD domain protein, DegV family | ||
BCJHNJMD_02033 | 7.6e-233 | yxiO | S | Vacuole effluxer Atg22 like | ||
BCJHNJMD_02034 | 3.2e-197 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
BCJHNJMD_02035 | 6.3e-70 | K | Transcriptional regulator | |||
BCJHNJMD_02036 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
BCJHNJMD_02037 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
BCJHNJMD_02038 | 4.4e-205 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
BCJHNJMD_02039 | 6.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
BCJHNJMD_02040 | 5.5e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
BCJHNJMD_02041 | 5.6e-80 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
BCJHNJMD_02042 | 7.5e-305 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
BCJHNJMD_02043 | 8.6e-56 | esbA | S | Family of unknown function (DUF5322) | ||
BCJHNJMD_02044 | 6.8e-66 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
BCJHNJMD_02045 | 5.8e-208 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
BCJHNJMD_02046 | 1.6e-111 | XK27_02070 | S | Nitroreductase family | ||
BCJHNJMD_02047 | 7.7e-86 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02048 | 1.3e-122 | S | CAAX protease self-immunity | |||
BCJHNJMD_02049 | 4.8e-52 | |||||
BCJHNJMD_02050 | 1.4e-82 | mutT | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
BCJHNJMD_02051 | 4.8e-28 | |||||
BCJHNJMD_02052 | 5.9e-247 | amtB | P | ammonium transporter | ||
BCJHNJMD_02053 | 3.7e-66 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
BCJHNJMD_02054 | 3e-220 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
BCJHNJMD_02056 | 6.4e-28 | 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 | ||
BCJHNJMD_02057 | 2.1e-105 | ypsA | S | Belongs to the UPF0398 family | ||
BCJHNJMD_02058 | 4.2e-112 | 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 | ||
BCJHNJMD_02059 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
BCJHNJMD_02060 | 1.7e-60 | P | Rhodanese Homology Domain | |||
BCJHNJMD_02061 | 3e-90 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
BCJHNJMD_02062 | 7.2e-124 | dnaD | L | Replication initiation and membrane attachment | ||
BCJHNJMD_02063 | 9.4e-209 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
BCJHNJMD_02064 | 2.6e-83 | ypmB | S | Protein conserved in bacteria | ||
BCJHNJMD_02065 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
BCJHNJMD_02066 | 4.5e-169 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
BCJHNJMD_02067 | 2.9e-171 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
BCJHNJMD_02068 | 2.4e-203 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
BCJHNJMD_02069 | 3.4e-186 | 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) | |
BCJHNJMD_02070 | 2e-266 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
BCJHNJMD_02071 | 7.3e-152 | yitU | 3.1.3.104 | S | hydrolase | |
BCJHNJMD_02072 | 6.2e-213 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BCJHNJMD_02073 | 8.6e-81 | |||||
BCJHNJMD_02074 | 1.8e-164 | S | Oxidoreductase, aldo keto reductase family protein | |||
BCJHNJMD_02075 | 3.8e-162 | akr5f | 1.1.1.346 | S | reductase | |
BCJHNJMD_02076 | 1.3e-77 | K | Transcriptional regulator | |||
BCJHNJMD_02077 | 5.1e-198 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
BCJHNJMD_02078 | 8.2e-48 | S | Uncharacterized protein conserved in bacteria (DUF2316) | |||
BCJHNJMD_02079 | 7.2e-66 | K | MarR family | |||
BCJHNJMD_02080 | 4.2e-77 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_02081 | 1.1e-99 | 1.1.1.219 | GM | Male sterility protein | ||
BCJHNJMD_02082 | 1.4e-181 | C | Zinc-binding dehydrogenase | |||
BCJHNJMD_02083 | 0.0 | kup | P | Transport of potassium into the cell | ||
BCJHNJMD_02084 | 2.7e-48 | yeaN | P | Major Facilitator Superfamily | ||
BCJHNJMD_02085 | 2.1e-200 | yjcE | P | Sodium proton antiporter | ||
BCJHNJMD_02086 | 2e-58 | yqkB | S | Belongs to the HesB IscA family | ||
BCJHNJMD_02087 | 4e-177 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
BCJHNJMD_02088 | 1.3e-111 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02089 | 4e-183 | ybhR | V | ABC transporter | ||
BCJHNJMD_02090 | 8.9e-125 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
BCJHNJMD_02091 | 6.1e-20 | S | Mor transcription activator family | |||
BCJHNJMD_02092 | 1.5e-121 | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
BCJHNJMD_02093 | 2.9e-41 | S | Mor transcription activator family | |||
BCJHNJMD_02094 | 6.4e-38 | S | Mor transcription activator family | |||
BCJHNJMD_02095 | 1.9e-68 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
BCJHNJMD_02096 | 2.1e-100 | bm3R1 | K | Psort location Cytoplasmic, score | ||
BCJHNJMD_02097 | 0.0 | yhcA | V | ABC transporter, ATP-binding protein | ||
BCJHNJMD_02098 | 2.4e-207 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
BCJHNJMD_02099 | 3.5e-60 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
BCJHNJMD_02100 | 3e-214 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
BCJHNJMD_02101 | 4.5e-98 | |||||
BCJHNJMD_02102 | 7.7e-198 | |||||
BCJHNJMD_02103 | 2.4e-27 | yozG | K | Transcriptional regulator | ||
BCJHNJMD_02104 | 1.3e-49 | S | Protein of unknown function (DUF2975) | |||
BCJHNJMD_02105 | 4.9e-295 | 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 | |
BCJHNJMD_02106 | 1.4e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
BCJHNJMD_02107 | 4.5e-155 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
BCJHNJMD_02108 | 1.3e-273 | pipD | E | Dipeptidase | ||
BCJHNJMD_02109 | 5.5e-278 | yjeM | E | Amino Acid | ||
BCJHNJMD_02110 | 1.2e-146 | K | Helix-turn-helix | |||
BCJHNJMD_02111 | 1.1e-35 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02112 | 1e-67 | npr | 1.11.1.1 | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
BCJHNJMD_02113 | 9e-69 | |||||
BCJHNJMD_02114 | 2.1e-102 | rimL | J | Acetyltransferase (GNAT) domain | ||
BCJHNJMD_02115 | 4.8e-295 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
BCJHNJMD_02116 | 3.4e-56 | K | GNAT family | |||
BCJHNJMD_02117 | 2.7e-88 | pnb | C | nitroreductase | ||
BCJHNJMD_02118 | 6.7e-187 | C | Aldo/keto reductase family | |||
BCJHNJMD_02119 | 3.1e-30 | adhR | K | MerR, DNA binding | ||
BCJHNJMD_02120 | 5.8e-41 | N | PFAM Uncharacterised protein family UPF0150 | |||
BCJHNJMD_02121 | 3e-156 | lmrB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_02122 | 4.1e-43 | merR | K | bacterial-type RNA polymerase transcription factor activity, metal ion regulated sequence-specific DNA binding | ||
BCJHNJMD_02123 | 9.2e-72 | K | LytTr DNA-binding domain | |||
BCJHNJMD_02124 | 2.4e-72 | S | Protein of unknown function (DUF3021) | |||
BCJHNJMD_02125 | 1.9e-48 | S | NADPH-dependent FMN reductase | |||
BCJHNJMD_02126 | 5.7e-115 | ydiC1 | EGP | Major facilitator Superfamily | ||
BCJHNJMD_02127 | 3.2e-22 | papX3 | K | Transcriptional regulator | ||
BCJHNJMD_02128 | 2.4e-31 | K | helix_turn_helix, mercury resistance | |||
BCJHNJMD_02129 | 7.9e-109 | S | NAD(P)H-binding | |||
BCJHNJMD_02130 | 1.3e-90 | entB | 3.5.1.19 | Q | Isochorismatase family | |
BCJHNJMD_02131 | 4.4e-52 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
BCJHNJMD_02132 | 2.2e-85 | bioY | S | BioY family | ||
BCJHNJMD_02133 | 3e-142 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
BCJHNJMD_02134 | 1.2e-119 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
BCJHNJMD_02135 | 1.7e-142 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
BCJHNJMD_02136 | 4.7e-154 | 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 | |
BCJHNJMD_02137 | 8.6e-265 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
BCJHNJMD_02138 | 5.5e-71 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
BCJHNJMD_02139 | 6.7e-72 | 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 | |
BCJHNJMD_02140 | 1.2e-227 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
BCJHNJMD_02141 | 6e-121 | IQ | reductase | |||
BCJHNJMD_02142 | 8.5e-165 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
BCJHNJMD_02143 | 2e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BCJHNJMD_02144 | 4.8e-182 | 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 | |
BCJHNJMD_02145 | 2.1e-79 | marR | K | Transcriptional regulator | ||
BCJHNJMD_02146 | 2.3e-75 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
BCJHNJMD_02147 | 1.7e-189 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
BCJHNJMD_02148 | 2.7e-58 | 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 | ||
BCJHNJMD_02149 | 4.5e-143 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
BCJHNJMD_02150 | 1.6e-91 | 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 | ||
BCJHNJMD_02151 | 1.9e-40 | ylqC | S | Belongs to the UPF0109 family | ||
BCJHNJMD_02152 | 3.8e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
BCJHNJMD_02153 | 6.1e-48 | |||||
BCJHNJMD_02154 | 1.3e-230 | S | Putative metallopeptidase domain | |||
BCJHNJMD_02155 | 1.4e-212 | 3.1.3.1 | S | associated with various cellular activities | ||
BCJHNJMD_02156 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
BCJHNJMD_02157 | 8.3e-207 | 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 | |
BCJHNJMD_02158 | 2.9e-57 | 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 | ||
BCJHNJMD_02159 | 4.6e-173 | 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) | ||
BCJHNJMD_02160 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
BCJHNJMD_02161 | 2.8e-128 | 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 | |
BCJHNJMD_02162 | 6.4e-38 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
BCJHNJMD_02163 | 1.4e-187 | 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 | |
BCJHNJMD_02164 | 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) | |
BCJHNJMD_02165 | 4.7e-311 | yloV | S | DAK2 domain fusion protein YloV | ||
BCJHNJMD_02166 | 5.2e-57 | asp | S | Asp23 family, cell envelope-related function | ||
BCJHNJMD_02167 | 4.9e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
BCJHNJMD_02168 | 4.4e-126 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
BCJHNJMD_02169 | 1.1e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
BCJHNJMD_02170 | 1.4e-167 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
BCJHNJMD_02171 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
BCJHNJMD_02172 | 1.5e-130 | stp | 3.1.3.16 | T | phosphatase | |
BCJHNJMD_02173 | 4.7e-150 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
BCJHNJMD_02174 | 3e-59 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
BCJHNJMD_02175 | 2.4e-170 | 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 | |
BCJHNJMD_02176 | 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 | ||
BCJHNJMD_02177 | 6.3e-216 | 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 | |
BCJHNJMD_02178 | 4.9e-31 | 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 | |
BCJHNJMD_02179 | 3.3e-104 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
BCJHNJMD_02180 | 1.1e-50 | |||||
BCJHNJMD_02182 | 3.6e-64 | M | domain protein | |||
BCJHNJMD_02183 | 8.8e-309 | recN | L | May be involved in recombinational repair of damaged DNA | ||
BCJHNJMD_02184 | 3.7e-76 | argR | K | Regulates arginine biosynthesis genes | ||
BCJHNJMD_02185 | 1.4e-147 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
BCJHNJMD_02186 | 1.6e-163 | 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 | |
BCJHNJMD_02187 | 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 | |
BCJHNJMD_02188 | 1e-243 | 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 | |
BCJHNJMD_02189 | 1.2e-155 | 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 | |
BCJHNJMD_02190 | 7.2e-74 | 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 | ||
BCJHNJMD_02191 | 4.8e-73 | yqhY | S | Asp23 family, cell envelope-related function | ||
BCJHNJMD_02192 | 1.3e-99 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
BCJHNJMD_02193 | 2e-189 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BCJHNJMD_02194 | 1.6e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
BCJHNJMD_02195 | 2.2e-57 | ysxB | J | Cysteine protease Prp | ||
BCJHNJMD_02196 | 3.4e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
BCJHNJMD_02197 | 2e-94 | K | Transcriptional regulator | |||
BCJHNJMD_02198 | 1.2e-94 | dut | S | Protein conserved in bacteria | ||
BCJHNJMD_02199 | 1.8e-178 | |||||
BCJHNJMD_02200 | 1.1e-156 | |||||
BCJHNJMD_02201 | 4.9e-262 | glnA | 6.3.1.2 | E | glutamine synthetase | |
BCJHNJMD_02202 | 2.1e-64 | glnR | K | Transcriptional regulator | ||
BCJHNJMD_02203 | 3.4e-169 | 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) | |
BCJHNJMD_02204 | 1.6e-140 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
BCJHNJMD_02205 | 3.1e-23 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
BCJHNJMD_02206 | 2.1e-70 | yqhL | P | Rhodanese-like protein | ||
BCJHNJMD_02207 | 1.2e-180 | glk | 2.7.1.2 | G | Glucokinase | |
BCJHNJMD_02208 | 9.3e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
BCJHNJMD_02209 | 9.9e-118 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
BCJHNJMD_02210 | 8.3e-91 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
BCJHNJMD_02211 | 2.5e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
BCJHNJMD_02212 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
BCJHNJMD_02213 | 6.5e-28 | CP_0775 | S | Domain of unknown function (DUF378) | ||
BCJHNJMD_02214 | 0.0 | S | membrane | |||
BCJHNJMD_02215 | 1.7e-56 | yneR | S | Belongs to the HesB IscA family | ||
BCJHNJMD_02216 | 6.3e-71 | 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 | ||
BCJHNJMD_02217 | 1e-119 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
BCJHNJMD_02218 | 3.8e-207 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
BCJHNJMD_02219 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BCJHNJMD_02220 | 3.8e-201 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
BCJHNJMD_02221 | 1.1e-67 | yodB | K | Transcriptional regulator, HxlR family | ||
BCJHNJMD_02222 | 2e-91 | 2.7.7.19, 2.7.7.72 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
BCJHNJMD_02223 | 1.6e-140 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
BCJHNJMD_02224 | 2.7e-42 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
BCJHNJMD_02225 | 2.6e-134 | 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 | ||
BCJHNJMD_02226 | 1.7e-69 | S | Protein of unknown function (DUF1093) | |||
BCJHNJMD_02227 | 9.3e-292 | arlS | 2.7.13.3 | T | Histidine kinase | |
BCJHNJMD_02228 | 2.8e-120 | K | response regulator | |||
BCJHNJMD_02229 | 1.9e-194 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
BCJHNJMD_02230 | 2.1e-21 | zmp3 | O | Zinc-dependent metalloprotease | ||
BCJHNJMD_02231 | 6.2e-67 | zmp3 | O | Zinc-dependent metalloprotease | ||
BCJHNJMD_02232 | 8.2e-51 | K | Transcriptional regulator, ArsR family | |||
BCJHNJMD_02233 | 4.6e-146 | 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | ||
BCJHNJMD_02234 | 6.9e-29 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
BCJHNJMD_02235 | 8.6e-96 | yceD | S | Uncharacterized ACR, COG1399 | ||
BCJHNJMD_02236 | 3.5e-216 | ylbM | S | Belongs to the UPF0348 family | ||
BCJHNJMD_02237 | 1.1e-138 | yqeM | Q | Methyltransferase | ||
BCJHNJMD_02238 | 1.6e-58 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
BCJHNJMD_02239 | 4e-107 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
BCJHNJMD_02240 | 5.9e-117 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
BCJHNJMD_02241 | 1.3e-48 | yhbY | J | RNA-binding protein | ||
BCJHNJMD_02242 | 1.9e-222 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
BCJHNJMD_02243 | 3.2e-103 | yqeG | S | HAD phosphatase, family IIIA | ||
BCJHNJMD_02244 | 3.2e-111 | S | regulation of response to stimulus | |||
BCJHNJMD_02245 | 3.7e-55 | 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 | ||
BCJHNJMD_02246 | 7.4e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
BCJHNJMD_02247 | 4.4e-79 | 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 | ||
BCJHNJMD_02248 | 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) | |
BCJHNJMD_02249 | 1.9e-164 | dnaI | L | Primosomal protein DnaI | ||
BCJHNJMD_02250 | 5e-246 | dnaB | L | replication initiation and membrane attachment | ||
BCJHNJMD_02251 | 7.8e-88 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
BCJHNJMD_02252 | 1.8e-110 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
BCJHNJMD_02253 | 3.3e-163 | 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 | |
BCJHNJMD_02254 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
BCJHNJMD_02255 | 2.7e-260 | guaD | 3.5.4.3 | F | Amidohydrolase family | |
BCJHNJMD_02256 | 3e-235 | F | Permease | |||
BCJHNJMD_02257 | 2.1e-118 | ybhL | S | Belongs to the BI1 family | ||
BCJHNJMD_02258 | 6.2e-134 | pnuC | H | nicotinamide mononucleotide transporter | ||
BCJHNJMD_02259 | 4.3e-258 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
BCJHNJMD_02260 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
BCJHNJMD_02261 | 5.3e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
BCJHNJMD_02262 | 4e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
BCJHNJMD_02263 | 2e-55 | ytzB | S | Small secreted protein | ||
BCJHNJMD_02264 | 3.2e-245 | cycA | E | Amino acid permease | ||
BCJHNJMD_02265 | 2.6e-200 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
BCJHNJMD_02266 | 8.2e-85 | uspA | T | Belongs to the universal stress protein A family | ||
BCJHNJMD_02267 | 1.5e-269 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
BCJHNJMD_02268 | 6.6e-148 | 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 | |
BCJHNJMD_02269 | 1.4e-124 | rluB | 5.4.99.19, 5.4.99.20, 5.4.99.21, 5.4.99.22 | J | pseudouridine synthase activity | |
BCJHNJMD_02270 | 1.5e-297 | ytgP | S | Polysaccharide biosynthesis protein | ||
BCJHNJMD_02271 | 4.4e-52 | |||||
BCJHNJMD_02272 | 4.8e-145 | S | NADPH-dependent FMN reductase | |||
BCJHNJMD_02273 | 2.7e-120 | P | ABC-type multidrug transport system ATPase component | |||
BCJHNJMD_02274 | 1e-46 | |||||
BCJHNJMD_02275 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BCJHNJMD_02276 | 3e-116 | pgpB1 | 3.6.1.27 | I | Acid phosphatase homologues | |
BCJHNJMD_02277 | 3.1e-101 | ytqB | J | Putative rRNA methylase | ||
BCJHNJMD_02279 | 2.3e-248 | pgaC | GT2 | M | Glycosyl transferase | |
BCJHNJMD_02280 | 2.6e-91 | |||||
BCJHNJMD_02281 | 5.1e-105 | T | EAL domain | |||
BCJHNJMD_02284 | 3.5e-11 | |||||
BCJHNJMD_02286 | 1.7e-71 | M | Mycoplasma protein of unknown function, DUF285 | |||
BCJHNJMD_02291 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
BCJHNJMD_02292 | 3.3e-75 | K | Acetyltransferase (GNAT) domain | |||
BCJHNJMD_02293 | 1.1e-166 | |||||
BCJHNJMD_02294 | 5.6e-108 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
BCJHNJMD_02296 | 5.1e-08 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | M | Bacterial surface protein 26-residue PARCEL repeat (3 repeats) | |
BCJHNJMD_02297 | 3.3e-22 | S | Mor transcription activator family | |||
BCJHNJMD_02298 | 7.6e-143 | ydhO | 3.4.14.13 | M | NlpC/P60 family | |
BCJHNJMD_02299 | 8.7e-219 | EGP | Major Facilitator Superfamily | |||
BCJHNJMD_02300 | 9.7e-85 | GM | NAD(P)H-binding | |||
BCJHNJMD_02301 | 1.1e-118 | lsa | S | ABC transporter | ||
BCJHNJMD_02302 | 1.1e-59 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02303 | 1.2e-184 | yfjF | U | Sugar (and other) transporter | ||
BCJHNJMD_02304 | 1.3e-79 | argO | S | LysE type translocator | ||
BCJHNJMD_02305 | 1.3e-35 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
BCJHNJMD_02306 | 4.3e-143 | nlhH | I | Esterase | ||
BCJHNJMD_02307 | 1.7e-176 | draG | 3.2.2.24 | O | ADP-ribosylglycohydrolase | |
BCJHNJMD_02308 | 4.9e-97 | yncA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
BCJHNJMD_02310 | 7.1e-85 | cadD | P | Cadmium resistance transporter | ||
BCJHNJMD_02311 | 7.7e-76 | lipB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
BCJHNJMD_02312 | 2.7e-75 | gtrA | S | GtrA-like protein | ||
BCJHNJMD_02313 | 3.5e-302 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
BCJHNJMD_02314 | 1.1e-113 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02315 | 7.3e-231 | XK27_06930 | S | ABC-2 family transporter protein | ||
BCJHNJMD_02316 | 2.2e-130 | qmcA | O | prohibitin homologues | ||
BCJHNJMD_02317 | 1.3e-54 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
BCJHNJMD_02318 | 6.2e-134 | |||||
BCJHNJMD_02319 | 4.5e-100 | GBS0088 | S | Nucleotidyltransferase | ||
BCJHNJMD_02320 | 3.7e-85 | yybC | S | Protein of unknown function (DUF2798) | ||
BCJHNJMD_02321 | 8.9e-57 | ydiI | Q | Thioesterase superfamily | ||
BCJHNJMD_02322 | 1.1e-155 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
BCJHNJMD_02323 | 1.7e-265 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
BCJHNJMD_02324 | 4.2e-95 | S | Protein of unknown function (DUF1097) | |||
BCJHNJMD_02325 | 3.3e-164 | |||||
BCJHNJMD_02326 | 1.8e-289 | 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 | |
BCJHNJMD_02327 | 1.2e-285 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
BCJHNJMD_02328 | 1.1e-209 | lmrP | E | Major Facilitator Superfamily | ||
BCJHNJMD_02331 | 4.8e-73 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
BCJHNJMD_02332 | 1.9e-10 | yobS | K | transcriptional regulator | ||
BCJHNJMD_02333 | 2.6e-56 | ywnB | S | NAD(P)H-binding | ||
BCJHNJMD_02334 | 8.9e-107 | dhaS | K | Bacterial regulatory proteins, tetR family | ||
BCJHNJMD_02335 | 5.8e-280 | E | amino acid | |||
BCJHNJMD_02336 | 6.5e-281 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
BCJHNJMD_02337 | 1.3e-295 | 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) | |
BCJHNJMD_02338 | 1e-173 | |||||
BCJHNJMD_02339 | 1.1e-17 | |||||
BCJHNJMD_02341 | 2.4e-95 | I | NUDIX domain | |||
BCJHNJMD_02342 | 8.1e-114 | yviA | S | Protein of unknown function (DUF421) | ||
BCJHNJMD_02343 | 1.3e-73 | S | Protein of unknown function (DUF3290) | |||
BCJHNJMD_02344 | 1.5e-166 | ropB | K | Helix-turn-helix XRE-family like proteins | ||
BCJHNJMD_02345 | 4.1e-218 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_02346 | 4.7e-249 | gshR | 1.8.1.7 | C | Glutathione reductase | |
BCJHNJMD_02347 | 9.1e-36 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
BCJHNJMD_02349 | 9.8e-198 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
BCJHNJMD_02350 | 1.8e-35 | |||||
BCJHNJMD_02351 | 4.2e-138 | kguE | 2.7.1.45 | G | Xylose isomerase domain protein TIM barrel | |
BCJHNJMD_02352 | 1.4e-232 | gntT | EG | Citrate transporter | ||
BCJHNJMD_02353 | 1.2e-177 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
BCJHNJMD_02354 | 7.2e-107 | hxlA | 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase HUMPS family | |
BCJHNJMD_02355 | 3.2e-87 | hxlB | 4.1.2.14, 4.1.2.43, 4.1.3.42, 5.3.1.27 | M | sugar phosphate isomerase involved in capsule formation | |
BCJHNJMD_02356 | 5.2e-176 | kdgR | K | helix_turn _helix lactose operon repressor | ||
BCJHNJMD_02357 | 4.3e-55 | |||||
BCJHNJMD_02358 | 1.4e-83 | |||||
BCJHNJMD_02359 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
BCJHNJMD_02361 | 1.2e-191 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
BCJHNJMD_02362 | 9.7e-169 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
BCJHNJMD_02363 | 7.2e-223 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
BCJHNJMD_02364 | 6e-177 | |||||
BCJHNJMD_02365 | 6.8e-130 | cobB | K | SIR2 family | ||
BCJHNJMD_02366 | 3.8e-51 | |||||
BCJHNJMD_02367 | 1.1e-161 | yunF | F | Protein of unknown function DUF72 | ||
BCJHNJMD_02368 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
BCJHNJMD_02369 | 1.8e-147 | tatD | L | hydrolase, TatD family | ||
BCJHNJMD_02370 | 4.3e-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 | |
BCJHNJMD_02371 | 1.3e-162 | 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 | |
BCJHNJMD_02372 | 4.3e-36 | veg | S | Biofilm formation stimulator VEG | ||
BCJHNJMD_02373 | 1.9e-163 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
BCJHNJMD_02374 | 7.1e-109 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
BCJHNJMD_02375 | 0.0 | yicI | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
BCJHNJMD_02376 | 1.8e-259 | xylP | G | MFS/sugar transport protein | ||
BCJHNJMD_02377 | 4.2e-209 | xylR | GK | ROK family | ||
BCJHNJMD_02378 | 2.7e-293 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
BCJHNJMD_02379 | 2.9e-165 | 2.7.1.2 | GK | ROK family | ||
BCJHNJMD_02380 | 3.7e-90 | |||||
BCJHNJMD_02382 | 2.2e-54 | V | Transport permease protein | |||
BCJHNJMD_02383 | 1.6e-88 | V | ABC transporter | |||
BCJHNJMD_02384 | 1.9e-85 | KTV | abc transporter atp-binding protein | |||
BCJHNJMD_02385 | 3.3e-154 | S | Prolyl oligopeptidase family | |||
BCJHNJMD_02386 | 1.6e-163 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
BCJHNJMD_02387 | 3e-130 | fhuC | P | ABC transporter | ||
BCJHNJMD_02388 | 1.1e-131 | znuB | U | ABC 3 transport family | ||
BCJHNJMD_02391 | 1.5e-144 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
BCJHNJMD_02392 | 3.8e-217 | 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 | |
BCJHNJMD_02393 | 5.5e-178 | 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) | |
BCJHNJMD_02394 | 9.7e-56 | S | Domain of unknown function (DUF3899) | |||
BCJHNJMD_02395 | 4.7e-70 | racA | K | helix_turn_helix, mercury resistance | ||
BCJHNJMD_02396 | 9.8e-132 | gntR | K | UbiC transcription regulator-associated domain protein | ||
BCJHNJMD_02397 | 0.0 | xpkA | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
BCJHNJMD_02398 | 1.9e-144 | yxeH | S | hydrolase | ||
BCJHNJMD_02399 | 9.7e-266 | ywfO | S | HD domain protein | ||
BCJHNJMD_02400 | 2.1e-149 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
BCJHNJMD_02401 | 4.9e-78 | ywiB | S | Domain of unknown function (DUF1934) | ||
BCJHNJMD_02402 | 5.8e-54 | 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 | ||
BCJHNJMD_02403 | 1.4e-308 | 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 | |
BCJHNJMD_02404 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BCJHNJMD_02405 | 4.6e-233 | |||||
BCJHNJMD_02406 | 1.3e-72 | K | Transcriptional regulator | |||
BCJHNJMD_02407 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
BCJHNJMD_02408 | 4.5e-129 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
BCJHNJMD_02409 | 0.0 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
BCJHNJMD_02410 | 1.1e-237 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
BCJHNJMD_02411 | 4.3e-42 | rpmE2 | J | Ribosomal protein L31 | ||
BCJHNJMD_02412 | 1.5e-116 | srtA | 3.4.22.70 | M | sortase family | |
BCJHNJMD_02413 | 3.4e-18 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_02414 | 9e-09 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_02415 | 3e-12 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_02416 | 7.2e-86 | XK27_00720 | S | regulation of response to stimulus | ||
BCJHNJMD_02418 | 1.7e-16 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_02419 | 3.7e-32 | S | WxL domain surface cell wall-binding | |||
BCJHNJMD_02420 | 4.4e-109 | S | Cell surface protein | |||
BCJHNJMD_02421 | 6.2e-110 | XK27_00720 | S | regulation of response to stimulus | ||
BCJHNJMD_02422 | 5.1e-237 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
BCJHNJMD_02423 | 1.8e-81 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
BCJHNJMD_02424 | 9.9e-95 | lemA | S | LemA family | ||
BCJHNJMD_02425 | 7.3e-145 | htpX | O | Belongs to the peptidase M48B family | ||
BCJHNJMD_02426 | 1.9e-149 | |||||
BCJHNJMD_02427 | 2.1e-255 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
BCJHNJMD_02428 | 2.1e-240 | 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 | |
BCJHNJMD_02429 | 8e-213 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
BCJHNJMD_02430 | 2.9e-63 | 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 | |
BCJHNJMD_02431 | 3.5e-213 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
BCJHNJMD_02433 | 3.6e-61 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
BCJHNJMD_02434 | 1.1e-113 | S | (CBS) domain | |||
BCJHNJMD_02436 | 3.2e-256 | S | Putative peptidoglycan binding domain | |||
BCJHNJMD_02437 | 2.2e-176 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
BCJHNJMD_02438 | 9.6e-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 | |
BCJHNJMD_02439 | 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 | ||
BCJHNJMD_02440 | 4.1e-292 | yabM | S | Polysaccharide biosynthesis protein | ||
BCJHNJMD_02441 | 1.6e-39 | yabO | J | S4 domain protein | ||
BCJHNJMD_02442 | 9.7e-44 | divIC | D | Septum formation initiator | ||
BCJHNJMD_02443 | 4.2e-71 | yabR | J | RNA binding | ||
BCJHNJMD_02444 | 2.4e-256 | 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 | |
BCJHNJMD_02445 | 1.3e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
BCJHNJMD_02446 | 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 | ||
BCJHNJMD_02447 | 7.7e-163 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
BCJHNJMD_02448 | 1.5e-194 | 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 | ||
BCJHNJMD_02457 | 1.7e-26 | S | Uncharacterized protein conserved in bacteria (DUF2188) | |||
BCJHNJMD_02459 | 4.1e-21 | K | Helix-turn-helix | |||
BCJHNJMD_02460 | 4.3e-43 | yvaO | K | Helix-turn-helix domain | ||
BCJHNJMD_02461 | 2.1e-46 | E | IrrE N-terminal-like domain | |||
BCJHNJMD_02463 | 9.5e-34 | |||||
BCJHNJMD_02465 | 2.2e-72 | sip | L | Belongs to the 'phage' integrase family | ||
BCJHNJMD_02467 | 1.7e-69 | S | MTH538 TIR-like domain (DUF1863) | |||
BCJHNJMD_02468 | 4.5e-163 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
BCJHNJMD_02469 | 5.4e-34 | |||||
BCJHNJMD_02471 | 1.1e-77 | T | Universal stress protein family | |||
BCJHNJMD_02472 | 1.6e-91 | 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 | |
BCJHNJMD_02473 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
BCJHNJMD_02474 | 1.5e-54 | yrvD | S | Pfam:DUF1049 | ||
BCJHNJMD_02475 | 5.7e-180 | 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 | |
BCJHNJMD_02476 | 5e-28 | |||||
BCJHNJMD_02477 | 6.2e-105 | |||||
BCJHNJMD_02478 | 1.3e-246 | 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 | ||
BCJHNJMD_02479 | 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 | ||
BCJHNJMD_02480 | 1.1e-15 | |||||
BCJHNJMD_02481 | 3.2e-52 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
BCJHNJMD_02482 | 6.6e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
BCJHNJMD_02483 | 6.9e-234 | 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 | ||
BCJHNJMD_02484 | 8.3e-222 | 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 | ||
BCJHNJMD_02485 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
BCJHNJMD_02486 | 3.1e-162 | S | Tetratricopeptide repeat | |||
BCJHNJMD_02487 | 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 | ||
BCJHNJMD_02488 | 1.3e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
BCJHNJMD_02489 | 2.1e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
BCJHNJMD_02490 | 2.1e-92 | |||||
BCJHNJMD_02491 | 1.2e-38 | K | transcriptional regulator | |||
BCJHNJMD_02492 | 7e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
BCJHNJMD_02493 | 0.0 | comEC | S | Competence protein ComEC | ||
BCJHNJMD_02494 | 1.2e-88 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
BCJHNJMD_02495 | 8.8e-106 | comEA | L | Competence protein ComEA | ||
BCJHNJMD_02496 | 2.4e-195 | ylbL | T | Belongs to the peptidase S16 family | ||
BCJHNJMD_02497 | 2.1e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
BCJHNJMD_02498 | 1.4e-98 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
BCJHNJMD_02499 | 4.4e-43 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
BCJHNJMD_02500 | 1.9e-209 | ftsW | D | Belongs to the SEDS family | ||
BCJHNJMD_02501 | 0.0 | typA | T | GTP-binding protein TypA | ||
BCJHNJMD_02502 | 6.7e-142 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
BCJHNJMD_02503 | 7.9e-45 | yktA | S | Belongs to the UPF0223 family | ||
BCJHNJMD_02504 | 2.3e-162 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
BCJHNJMD_02505 | 4.4e-269 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
BCJHNJMD_02506 | 5.4e-205 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
BCJHNJMD_02507 | 4.8e-182 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
BCJHNJMD_02508 | 7e-214 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
BCJHNJMD_02509 | 2.8e-102 | 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 | |
BCJHNJMD_02510 | 3.1e-68 | |||||
BCJHNJMD_02511 | 1.2e-32 | ykzG | S | Belongs to the UPF0356 family | ||
BCJHNJMD_02512 | 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 | ||
BCJHNJMD_02513 | 2.4e-186 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic | |
BCJHNJMD_02514 | 1.3e-28 | |||||
BCJHNJMD_02515 | 6.3e-107 | mltD | CBM50 | M | NlpC P60 family protein | |
BCJHNJMD_02516 | 8.8e-166 | ypuA | S | Protein of unknown function (DUF1002) | ||
BCJHNJMD_02517 | 1.2e-168 | ykfC | 3.4.14.13 | M | NlpC/P60 family | |
BCJHNJMD_02518 | 0.0 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
BCJHNJMD_02519 | 2.8e-160 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
BCJHNJMD_02520 | 1.4e-184 | rbsR | K | helix_turn _helix lactose operon repressor | ||
BCJHNJMD_02521 | 3.1e-189 | yghZ | C | Aldo keto reductase family protein | ||
BCJHNJMD_02522 | 5.5e-156 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
BCJHNJMD_02523 | 2.3e-306 | E | ABC transporter, substratebinding protein | |||
BCJHNJMD_02524 | 1.1e-273 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
BCJHNJMD_02525 | 1.3e-159 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
BCJHNJMD_02526 | 2.5e-121 | yecS | E | ABC transporter permease | ||
BCJHNJMD_02527 | 1.2e-126 | yoaK | S | Protein of unknown function (DUF1275) | ||
BCJHNJMD_02528 | 1.4e-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) | |
BCJHNJMD_02529 | 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 | |
BCJHNJMD_02530 | 2.3e-119 | S | Repeat protein | |||
BCJHNJMD_02531 | 3.5e-120 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
BCJHNJMD_02532 | 3e-223 | 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 | |
BCJHNJMD_02533 | 1.5e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
BCJHNJMD_02534 | 2.6e-222 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
BCJHNJMD_02535 | 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 | |
BCJHNJMD_02536 | 5.2e-31 | |||||
BCJHNJMD_02537 | 4.2e-95 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
BCJHNJMD_02538 | 2.2e-34 | cspA | K | Cold shock protein | ||
BCJHNJMD_02539 | 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) | |
BCJHNJMD_02540 | 3.3e-92 | divIVA | D | DivIVA domain protein | ||
BCJHNJMD_02541 | 5.4e-144 | ylmH | S | S4 domain protein | ||
BCJHNJMD_02542 | 4.1e-41 | yggT | S | YGGT family | ||
BCJHNJMD_02543 | 2.5e-74 | 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 | ||
BCJHNJMD_02544 | 3.2e-215 | 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 | ||
BCJHNJMD_02545 | 6e-244 | 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 | ||
BCJHNJMD_02546 | 1.7e-146 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
BCJHNJMD_02547 | 3.7e-199 | 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) |
BCJHNJMD_02548 | 1.4e-248 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
BCJHNJMD_02549 | 1.9e-183 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
BCJHNJMD_02550 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
BCJHNJMD_02551 | 3.2e-60 | ftsL | D | Cell division protein FtsL | ||
BCJHNJMD_02552 | 5.5e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
BCJHNJMD_02553 | 2e-79 | mraZ | K | Belongs to the MraZ family | ||
BCJHNJMD_02554 | 7.5e-61 | S | Protein of unknown function (DUF3397) | |||
BCJHNJMD_02555 | 2.2e-12 | S | Protein of unknown function (DUF4044) | |||
BCJHNJMD_02556 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
BCJHNJMD_02557 | 2.7e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
BCJHNJMD_02558 | 9.4e-158 | rrmA | 2.1.1.187 | H | Methyltransferase | |
BCJHNJMD_02559 | 4.6e-203 | XK27_05220 | S | AI-2E family transporter | ||
BCJHNJMD_02560 | 1.1e-107 | cutC | P | Participates in the control of copper homeostasis | ||
BCJHNJMD_02561 | 6.5e-17 | tagE1 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
BCJHNJMD_02562 | 2.1e-269 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
BCJHNJMD_02563 | 2.1e-269 | tagE2 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
BCJHNJMD_02564 | 7.8e-26 | |||||
BCJHNJMD_02565 | 4.9e-58 | S | Pfam Methyltransferase | |||
BCJHNJMD_02566 | 3.6e-61 | alr | 5.1.1.1, 6.3.2.10 | M | UDP-N-acetylmuramoyl-tripeptide-D-alanyl-D-alanine ligase activity | |
BCJHNJMD_02567 | 1.7e-64 | 3.1.3.18 | S | Pfam Methyltransferase | ||
BCJHNJMD_02568 | 1.5e-16 | 3.1.3.18 | S | Pfam Methyltransferase | ||
BCJHNJMD_02569 | 2.9e-173 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
BCJHNJMD_02570 | 1.5e-149 | 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 | |
BCJHNJMD_02571 | 3.3e-118 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
BCJHNJMD_02572 | 5.8e-112 | yjbH | Q | Thioredoxin | ||
BCJHNJMD_02573 | 2.5e-158 | degV | S | DegV family | ||
BCJHNJMD_02574 | 0.0 | pepF | E | oligoendopeptidase F | ||
BCJHNJMD_02575 | 3e-201 | coiA | 3.6.4.12 | S | Competence protein | |
BCJHNJMD_02576 | 8.8e-124 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
BCJHNJMD_02577 | 1.9e-149 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
BCJHNJMD_02578 | 3.2e-220 | ecsB | U | ABC transporter | ||
BCJHNJMD_02579 | 1.6e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
BCJHNJMD_02580 | 1.5e-82 | hit | FG | histidine triad | ||
BCJHNJMD_02581 | 1.7e-48 | |||||
BCJHNJMD_02582 | 9.1e-151 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
BCJHNJMD_02583 | 6e-185 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |||
BCJHNJMD_02584 | 0.0 | L | AAA domain | |||
BCJHNJMD_02585 | 3.7e-232 | yhaO | L | Ser Thr phosphatase family protein | ||
BCJHNJMD_02586 | 1.8e-51 | yheA | S | Belongs to the UPF0342 family | ||
BCJHNJMD_02587 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
BCJHNJMD_02588 | 4.7e-79 | argR | K | Regulates arginine biosynthesis genes | ||
BCJHNJMD_02589 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
BCJHNJMD_02591 | 1.1e-17 | |||||
BCJHNJMD_02592 | 3.2e-231 | 3.2.1.96, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
BCJHNJMD_02593 | 3.7e-96 | 1.5.1.3 | H | RibD C-terminal domain | ||
BCJHNJMD_02594 | 1.1e-53 | S | Protein of unknown function (DUF1516) | |||
BCJHNJMD_02595 | 4.8e-107 | 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BCJHNJMD_02596 | 5.2e-216 | 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) | |
BCJHNJMD_02597 | 3.1e-252 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
BCJHNJMD_02598 | 8.1e-188 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
BCJHNJMD_02599 | 4e-23 | ulaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
BCJHNJMD_02600 | 3.2e-32 | 2.7.1.194, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
BCJHNJMD_02601 | 1.8e-130 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
BCJHNJMD_02602 | 3.6e-251 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
BCJHNJMD_02603 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
BCJHNJMD_02604 | 3.1e-119 | ntcA2 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
BCJHNJMD_02605 | 5.5e-272 | pipD | E | Peptidase family C69 | ||
BCJHNJMD_02606 | 1.3e-37 | |||||
BCJHNJMD_02607 | 0.0 | |||||
BCJHNJMD_02608 | 5.7e-50 | S | Leucine-rich repeat (LRR) protein | |||
BCJHNJMD_02611 | 0.0 | uvrA3 | L | ABC transporter | ||
BCJHNJMD_02613 | 7.5e-88 | 3.2.1.17 | M | hydrolase, family 25 | ||
BCJHNJMD_02614 | 1.8e-40 | |||||
BCJHNJMD_02615 | 1.8e-38 | M | Mycoplasma protein of unknown function, DUF285 | |||
BCJHNJMD_02616 | 6.3e-221 | L | Transposase | |||
BCJHNJMD_02617 | 1.1e-58 | 3.6.4.12 | L | UvrD/REP helicase N-terminal domain | ||
BCJHNJMD_02618 | 4.7e-131 | L | AAA ATPase domain | |||
BCJHNJMD_02619 | 2.8e-61 | |||||
BCJHNJMD_02620 | 2.3e-53 | |||||
BCJHNJMD_02621 | 3.2e-250 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
BCJHNJMD_02622 | 5.9e-280 | S | Protein of unknown function DUF262 | |||
BCJHNJMD_02623 | 5e-16 | |||||
BCJHNJMD_02624 | 1.3e-11 | S | Transglycosylase associated protein | |||
BCJHNJMD_02625 | 4.2e-34 | S | Asp23 family, cell envelope-related function | |||
BCJHNJMD_02626 | 5.5e-82 | S | membrane | |||
BCJHNJMD_02627 | 5.6e-39 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02628 | 1.2e-58 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
BCJHNJMD_02629 | 4e-56 | K | helix_turn_helix multiple antibiotic resistance protein | |||
BCJHNJMD_02630 | 7.8e-97 | tnpR1 | L | Resolvase, N terminal domain | ||
BCJHNJMD_02631 | 1.2e-23 | S | Family of unknown function (DUF5388) | |||
BCJHNJMD_02632 | 5.5e-144 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
BCJHNJMD_02635 | 4.6e-71 | pi346 | L | IstB-like ATP binding protein | ||
BCJHNJMD_02636 | 5.1e-48 | S | calcium ion binding | |||
BCJHNJMD_02638 | 4.1e-53 | S | Transcriptional regulator, RinA family | |||
BCJHNJMD_02641 | 2.6e-43 | S | YopX protein | |||
BCJHNJMD_02646 | 4.8e-46 | S | N-terminal phage replisome organiser (Phage_rep_org_N) | |||
BCJHNJMD_02653 | 3.2e-30 | 3.4.22.70 | M | by MetaGeneAnnotator | ||
BCJHNJMD_02655 | 1.3e-138 | clpB | O | C-terminal, D2-small domain, of ClpB protein | ||
BCJHNJMD_02657 | 2e-92 | topB | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
BCJHNJMD_02658 | 8e-70 | L | Protein of unknown function (DUF3991) | |||
BCJHNJMD_02660 | 2.2e-24 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
BCJHNJMD_02669 | 5.1e-35 | S | Protein of unknown function (DUF3102) | |||
BCJHNJMD_02670 | 4.2e-108 | K | Primase C terminal 1 (PriCT-1) | |||
BCJHNJMD_02671 | 2.4e-98 | D | Cellulose biosynthesis protein BcsQ | |||
BCJHNJMD_02672 | 6.1e-45 | |||||
BCJHNJMD_02679 | 1.3e-83 | zmp2 | O | Zinc-dependent metalloprotease | ||
BCJHNJMD_02680 | 1.7e-51 | ybjQ | S | Belongs to the UPF0145 family | ||
BCJHNJMD_02681 | 6.8e-96 | |||||
BCJHNJMD_02682 | 1.2e-44 | |||||
BCJHNJMD_02683 | 9.6e-108 | |||||
BCJHNJMD_02684 | 8.3e-213 | 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 | |
BCJHNJMD_02685 | 1.1e-246 | bmr3 | EGP | Major facilitator Superfamily | ||
BCJHNJMD_02686 | 1.8e-56 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
BCJHNJMD_02687 | 4.5e-120 | dck | 2.7.1.74 | F | Deoxynucleoside kinase | |
BCJHNJMD_02688 | 7.7e-143 | S | haloacid dehalogenase-like hydrolase | |||
BCJHNJMD_02689 | 2.8e-101 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
BCJHNJMD_02690 | 0.0 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
BCJHNJMD_02691 | 4.3e-175 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
BCJHNJMD_02692 | 1.5e-36 | |||||
BCJHNJMD_02693 | 5.6e-121 | S | CAAX protease self-immunity | |||
BCJHNJMD_02694 | 9.4e-83 | ohrR | K | Transcriptional regulator | ||
BCJHNJMD_02695 | 4.6e-83 | V | VanZ like family | |||
BCJHNJMD_02696 | 5.1e-47 | |||||
BCJHNJMD_02698 | 2.6e-70 | int | L | Belongs to the 'phage' integrase family | ||
BCJHNJMD_02699 | 3.6e-49 | KLT | serine threonine protein kinase | |||
BCJHNJMD_02700 | 2.6e-35 | 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 | ||
BCJHNJMD_02701 | 1.2e-07 | yicL | EG | EamA-like transporter family | ||
BCJHNJMD_02705 | 1.6e-12 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
BCJHNJMD_02707 | 1.1e-81 | K | ORF6N domain | |||
BCJHNJMD_02712 | 2.7e-10 | 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 | |
BCJHNJMD_02715 | 7.7e-48 | S | Siphovirus Gp157 | |||
BCJHNJMD_02716 | 8e-29 | S | ERF superfamily | |||
BCJHNJMD_02717 | 1.6e-52 | 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 | ||
BCJHNJMD_02718 | 1.8e-37 | L | NUMOD4 motif | |||
BCJHNJMD_02721 | 3.2e-157 | S | phage terminase, large subunit | |||
BCJHNJMD_02722 | 3.8e-18 | L | Terminase, small subunit | |||
BCJHNJMD_02725 | 2.2e-25 | S | Protein of unknown function (DUF2829) | |||
BCJHNJMD_02727 | 2.9e-45 | S | Bacterial mobilisation protein (MobC) | |||
BCJHNJMD_02728 | 3.7e-52 | D | Relaxase/Mobilisation nuclease domain | |||
BCJHNJMD_02730 | 1.5e-79 | repB | L | Initiator Replication protein | ||
BCJHNJMD_02732 | 1.8e-58 | |||||
BCJHNJMD_02734 | 2.6e-26 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
BCJHNJMD_02735 | 1.2e-09 | |||||
BCJHNJMD_02736 | 4.3e-26 | J | tRNA cytidylyltransferase activity | |||
BCJHNJMD_02737 | 8.5e-26 | tnp | L | DDE domain | ||
BCJHNJMD_02738 | 2.6e-68 | tnp | L | DDE domain | ||
BCJHNJMD_02739 | 3.3e-14 | |||||
BCJHNJMD_02742 | 1.2e-12 | K | Helix-turn-helix domain | |||
BCJHNJMD_02747 | 2.3e-22 | V | endonuclease distantly related to archaeal Holliday junction resolvase and Mrr-like restriction enzymes | |||
BCJHNJMD_02748 | 1.8e-103 | L | Belongs to the 'phage' integrase family | |||
BCJHNJMD_02751 | 6.3e-82 | GT4 | M | Glycosyltransferase Family 4 | ||
BCJHNJMD_02752 | 7.8e-79 | tagA | 2.4.1.187 | GT26 | M | Belongs to the glycosyltransferase 26 family |
BCJHNJMD_02753 | 5.5e-84 | rfbP | M | Bacterial sugar transferase | ||
BCJHNJMD_02754 | 6.8e-139 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
BCJHNJMD_02755 | 8.2e-129 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
BCJHNJMD_02756 | 3.5e-90 | epsB | M | biosynthesis protein | ||
BCJHNJMD_02757 | 8e-159 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
BCJHNJMD_02758 | 1.1e-189 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
BCJHNJMD_02759 | 1.5e-253 | yfnA | E | Amino Acid | ||
BCJHNJMD_02760 | 4.6e-196 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
BCJHNJMD_02761 | 2.2e-79 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
BCJHNJMD_02762 | 2.4e-220 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
BCJHNJMD_02763 | 3.9e-102 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
BCJHNJMD_02764 | 3e-198 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
BCJHNJMD_02765 | 1.8e-116 | ktrA | P | domain protein | ||
BCJHNJMD_02766 | 1.4e-240 | ktrB | P | Potassium uptake protein | ||
BCJHNJMD_02767 | 9.2e-194 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
BCJHNJMD_02768 | 4.7e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
BCJHNJMD_02769 | 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 | ||
BCJHNJMD_02770 | 2.5e-152 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
BCJHNJMD_02771 | 1e-142 | 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 | ||
BCJHNJMD_02772 | 2.4e-161 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
BCJHNJMD_02773 | 9.9e-152 | cbiO | 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 | ||
BCJHNJMD_02774 | 7.4e-62 | rplQ | J | Ribosomal protein L17 | ||
BCJHNJMD_02775 | 9.7e-172 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
BCJHNJMD_02776 | 7.5e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
BCJHNJMD_02777 | 1.3e-60 | 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 | ||
BCJHNJMD_02778 | 1.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
BCJHNJMD_02779 | 3.4e-123 | 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 | |
BCJHNJMD_02780 | 1.2e-233 | 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 | ||
BCJHNJMD_02781 | 4.1e-69 | rplO | J | Binds to the 23S rRNA | ||
BCJHNJMD_02782 | 3.8e-24 | rpmD | J | Ribosomal protein L30 | ||
BCJHNJMD_02783 | 2.4e-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 | ||
BCJHNJMD_02784 | 6.6e-57 | 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 | ||
BCJHNJMD_02785 | 3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
BCJHNJMD_02786 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
BCJHNJMD_02787 | 2.1e-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 | ||
BCJHNJMD_02788 | 1.8e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
BCJHNJMD_02789 | 4.3e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
BCJHNJMD_02790 | 1.9e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
BCJHNJMD_02791 | 4.8e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
BCJHNJMD_02792 | 7.8e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
BCJHNJMD_02793 | 5.1e-119 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
BCJHNJMD_02794 | 2.4e-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 | ||
BCJHNJMD_02795 | 1.8e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
BCJHNJMD_02796 | 7.9e-149 | 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 | ||
BCJHNJMD_02797 | 2e-43 | 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 | ||
BCJHNJMD_02798 | 3.2e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
BCJHNJMD_02799 | 6.1e-117 | 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 | ||
BCJHNJMD_02800 | 8.9e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
BCJHNJMD_02801 | 2.4e-229 | mepA | V | MATE efflux family protein | ||
BCJHNJMD_02802 | 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 | ||
BCJHNJMD_02803 | 3.2e-83 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
BCJHNJMD_02804 | 1.2e-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 | ||
BCJHNJMD_02805 | 8.5e-111 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
BCJHNJMD_02806 | 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 | |
BCJHNJMD_02807 | 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 | |
BCJHNJMD_02808 | 1.9e-104 | K | Bacterial regulatory proteins, tetR family | |||
BCJHNJMD_02809 | 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 | ||
BCJHNJMD_02810 | 9.9e-77 | ctsR | K | Belongs to the CtsR family | ||
BCJHNJMD_02819 | 5.8e-212 | 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) | |
BCJHNJMD_02820 | 9.5e-115 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
BCJHNJMD_02821 | 4.8e-274 | lysP | E | amino acid | ||
BCJHNJMD_02822 | 8e-25 | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
BCJHNJMD_02823 | 1.6e-148 | I | alpha/beta hydrolase fold | |||
BCJHNJMD_02824 | 9.4e-121 | lssY | 3.6.1.27 | I | phosphatase | |
BCJHNJMD_02825 | 1.1e-72 | S | Threonine/Serine exporter, ThrE | |||
BCJHNJMD_02826 | 6.2e-121 | thrE | S | Putative threonine/serine exporter | ||
BCJHNJMD_02827 | 5.3e-121 | sirR | K | iron dependent repressor | ||
BCJHNJMD_02828 | 1.2e-158 | czcD | P | cation diffusion facilitator family transporter | ||
BCJHNJMD_02829 | 1.3e-102 | K | Acetyltransferase (GNAT) domain | |||
BCJHNJMD_02830 | 9.6e-74 | merR | K | MerR HTH family regulatory protein | ||
BCJHNJMD_02831 | 1.6e-266 | lmrB | EGP | Major facilitator Superfamily | ||
BCJHNJMD_02832 | 2.8e-102 | S | Domain of unknown function (DUF4811) | |||
BCJHNJMD_02833 | 1e-37 | yyaN | K | MerR HTH family regulatory protein | ||
BCJHNJMD_02834 | 1.3e-107 | azlC | E | branched-chain amino acid | ||
BCJHNJMD_02835 | 2.8e-49 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
BCJHNJMD_02836 | 2e-233 | pyrP | F | Permease | ||
BCJHNJMD_02837 | 1.1e-217 | EGP | Major facilitator Superfamily | |||
BCJHNJMD_02838 | 1e-69 | |||||
BCJHNJMD_02839 | 5.1e-90 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
BCJHNJMD_02840 | 1.2e-85 | nimA | S | resistance protein | ||
BCJHNJMD_02841 | 1.8e-104 | 3.2.2.20 | K | acetyltransferase | ||
BCJHNJMD_02842 | 7.2e-141 | yejC | S | Protein of unknown function (DUF1003) | ||
BCJHNJMD_02843 | 1.5e-163 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
BCJHNJMD_02844 | 1.4e-53 | S | Glycine cleavage H-protein | |||
BCJHNJMD_02847 | 1.6e-89 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
BCJHNJMD_02848 | 5e-281 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
BCJHNJMD_02849 | 3.2e-138 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
BCJHNJMD_02850 | 1.1e-263 | araB | 2.7.1.16 | G | carbohydrate kinase FGGY | |
BCJHNJMD_02851 | 0.0 | |||||
BCJHNJMD_02852 | 2.7e-131 | yisR | K | helix_turn_helix, arabinose operon control protein | ||
BCJHNJMD_02853 | 7.1e-216 | G | symporter | |||
BCJHNJMD_02854 | 8.2e-70 | K | sequence-specific DNA binding | |||
BCJHNJMD_02855 | 1.2e-256 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
BCJHNJMD_02856 | 2e-10 | |||||
BCJHNJMD_02857 | 1.2e-213 | melB | G | symporter | ||
BCJHNJMD_02858 | 8.7e-177 | araR | K | Transcriptional regulator | ||
BCJHNJMD_02859 | 3.8e-146 | K | transcriptional regulator, ArsR family | |||
BCJHNJMD_02860 | 1.3e-200 | abf | G | Belongs to the glycosyl hydrolase 43 family | ||
BCJHNJMD_02861 | 6.9e-237 | lacY | G | Oligosaccharide H symporter | ||
BCJHNJMD_02862 | 2.8e-298 | abfA | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
BCJHNJMD_02863 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
BCJHNJMD_02864 | 6.2e-70 | K | Transcriptional regulator | |||
BCJHNJMD_02865 | 9.3e-93 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
BCJHNJMD_02866 | 1.8e-278 | pipD | E | Dipeptidase | ||
BCJHNJMD_02867 | 5.3e-263 | arcD | E | Arginine ornithine antiporter | ||
BCJHNJMD_02868 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
BCJHNJMD_02869 | 1.1e-71 | S | Iron-sulphur cluster biosynthesis | |||
BCJHNJMD_02871 | 4.4e-75 | S | Peptidase_C39 like family | |||
BCJHNJMD_02872 | 2.2e-96 | M | NlpC/P60 family | |||
BCJHNJMD_02873 | 3.7e-20 | K | Helix-turn-helix domain | |||
BCJHNJMD_02874 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
BCJHNJMD_02875 | 8.4e-57 | bipA | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | M | Leucine-rich repeat (LRR) protein |
BCJHNJMD_02876 | 8.3e-09 | |||||
BCJHNJMD_02877 | 3e-95 | |||||
BCJHNJMD_02883 | 3.7e-118 | U | TraM recognition site of TraD and TraG | |||
BCJHNJMD_02886 | 2e-19 | I | mechanosensitive ion channel activity | |||
BCJHNJMD_02889 | 5.6e-129 | U | type IV secretory pathway VirB4 | |||
BCJHNJMD_02890 | 6.5e-48 | M | CHAP domain | |||
BCJHNJMD_02892 | 1.8e-18 | |||||
BCJHNJMD_02895 | 2.1e-96 | 2.1.1.72, 3.1.21.3 | AA10,CBM73 | L | Belongs to the N(4) N(6)-methyltransferase family | |
BCJHNJMD_02898 | 1.1e-54 | L | recombinase activity | |||
BCJHNJMD_02899 | 5.5e-172 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
BCJHNJMD_02901 | 5.8e-58 | M | Phage tail tape measure protein TP901 | |||
BCJHNJMD_02902 | 2.5e-26 | M | LysM domain | |||
BCJHNJMD_02903 | 5.1e-09 | |||||
BCJHNJMD_02904 | 1.9e-58 | |||||
BCJHNJMD_02905 | 1.1e-11 | |||||
BCJHNJMD_02907 | 1.3e-67 | Z012_12235 | S | Baseplate J-like protein | ||
BCJHNJMD_02910 | 1.9e-26 | |||||
BCJHNJMD_02912 | 1.6e-33 | |||||
BCJHNJMD_02917 | 1.1e-50 | S | Transcriptional regulator, RinA family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)