ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
FPANIOMK_00001 | 4.6e-188 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
FPANIOMK_00002 | 1.2e-155 | sapF | E | ATPases associated with a variety of cellular activities | ||
FPANIOMK_00003 | 5.2e-142 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
FPANIOMK_00004 | 5.4e-162 | EP | Binding-protein-dependent transport system inner membrane component | |||
FPANIOMK_00005 | 4.6e-169 | P | Binding-protein-dependent transport system inner membrane component | |||
FPANIOMK_00006 | 4.6e-310 | E | ABC transporter, substrate-binding protein, family 5 | |||
FPANIOMK_00007 | 3.6e-143 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
FPANIOMK_00008 | 2.8e-276 | G | Bacterial extracellular solute-binding protein | |||
FPANIOMK_00009 | 3.8e-66 | G | carbohydrate transport | |||
FPANIOMK_00010 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
FPANIOMK_00011 | 7.6e-126 | G | ABC transporter permease | |||
FPANIOMK_00012 | 2.9e-190 | K | Periplasmic binding protein domain | |||
FPANIOMK_00013 | 7.7e-21 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
FPANIOMK_00014 | 0.0 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
FPANIOMK_00016 | 3.2e-41 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
FPANIOMK_00017 | 7.5e-178 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
FPANIOMK_00018 | 3.2e-108 | cas4 | 3.1.12.1 | L | Domain of unknown function DUF83 | |
FPANIOMK_00019 | 2.1e-147 | cas7c | L | CRISPR-associated protein Cas7 | ||
FPANIOMK_00020 | 2.3e-243 | csd1 | S | CRISPR-associated protein (Cas_Csd1) | ||
FPANIOMK_00021 | 4.7e-101 | cas5d | S | CRISPR-associated protein (Cas_Cas5) | ||
FPANIOMK_00022 | 8.7e-310 | L | DEAD-like helicases superfamily | |||
FPANIOMK_00023 | 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) | |
FPANIOMK_00024 | 5e-55 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
FPANIOMK_00025 | 9.3e-275 | aldH | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | |
FPANIOMK_00026 | 4.1e-127 | XK27_08050 | O | prohibitin homologues | ||
FPANIOMK_00027 | 2.2e-243 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
FPANIOMK_00028 | 1.2e-233 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
FPANIOMK_00029 | 2.4e-259 | nox | 1.6.3.4 | C | Pyridine nucleotide-disulphide oxidoreductase | |
FPANIOMK_00030 | 9.9e-225 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
FPANIOMK_00031 | 0.0 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
FPANIOMK_00032 | 0.0 | ctpE | P | E1-E2 ATPase | ||
FPANIOMK_00033 | 6.4e-54 | racA | K | MerR, DNA binding | ||
FPANIOMK_00034 | 1.6e-196 | yghZ | C | Aldo/keto reductase family | ||
FPANIOMK_00035 | 5.1e-101 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
FPANIOMK_00036 | 4.1e-250 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
FPANIOMK_00037 | 1.1e-149 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
FPANIOMK_00038 | 1.1e-121 | S | Short repeat of unknown function (DUF308) | |||
FPANIOMK_00039 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
FPANIOMK_00040 | 8.5e-101 | L | Single-strand binding protein family | |||
FPANIOMK_00041 | 2.6e-43 | |||||
FPANIOMK_00042 | 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 | |
FPANIOMK_00043 | 2.5e-23 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
FPANIOMK_00044 | 4.2e-272 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
FPANIOMK_00045 | 8.4e-159 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
FPANIOMK_00046 | 2.8e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
FPANIOMK_00047 | 1.4e-109 | KT | Transcriptional regulatory protein, C terminal | |||
FPANIOMK_00048 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
FPANIOMK_00049 | 4.1e-289 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
FPANIOMK_00050 | 1.5e-190 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
FPANIOMK_00051 | 5.2e-116 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
FPANIOMK_00052 | 1e-49 | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | ||
FPANIOMK_00053 | 1.2e-185 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
FPANIOMK_00054 | 1.2e-189 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
FPANIOMK_00055 | 3.9e-36 | rpmE | J | Binds the 23S rRNA | ||
FPANIOMK_00057 | 4.4e-59 | K | helix_turn_helix, arabinose operon control protein | |||
FPANIOMK_00058 | 1.8e-136 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
FPANIOMK_00059 | 1.3e-254 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
FPANIOMK_00060 | 4.3e-108 | |||||
FPANIOMK_00061 | 1.6e-168 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
FPANIOMK_00062 | 4.7e-141 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
FPANIOMK_00063 | 1e-303 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
FPANIOMK_00064 | 9.4e-164 | EG | EamA-like transporter family | |||
FPANIOMK_00066 | 1.6e-149 | V | FtsX-like permease family | |||
FPANIOMK_00067 | 1.5e-147 | S | Sulfite exporter TauE/SafE | |||
FPANIOMK_00069 | 3.5e-213 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
FPANIOMK_00070 | 1.7e-251 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
FPANIOMK_00071 | 4.6e-35 | 1.1.1.122, 1.1.1.65 | C | Aldo/keto reductase family | ||
FPANIOMK_00072 | 3.3e-50 | EGP | Major facilitator superfamily | |||
FPANIOMK_00073 | 1.2e-11 | EGP | Major facilitator superfamily | |||
FPANIOMK_00074 | 5.2e-10 | K | Winged helix DNA-binding domain | |||
FPANIOMK_00075 | 3.7e-179 | glkA | 2.7.1.2 | G | ROK family | |
FPANIOMK_00076 | 2.4e-300 | S | ATPases associated with a variety of cellular activities | |||
FPANIOMK_00077 | 4.6e-55 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00078 | 1.7e-159 | I | alpha/beta hydrolase fold | |||
FPANIOMK_00079 | 6.5e-116 | S | Pyridoxamine 5'-phosphate oxidase | |||
FPANIOMK_00081 | 3.9e-49 | S | DUF218 domain | |||
FPANIOMK_00082 | 4.4e-18 | S | Protein of unknown function (DUF979) | |||
FPANIOMK_00083 | 6.7e-116 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
FPANIOMK_00084 | 5.7e-126 | |||||
FPANIOMK_00085 | 2.3e-159 | M | domain, Protein | |||
FPANIOMK_00086 | 4e-19 | M | domain, Protein | |||
FPANIOMK_00087 | 2.4e-306 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
FPANIOMK_00088 | 0.0 | 3.2.1.52, 3.2.1.83 | GH16,GH20 | G | hydrolase family 20, catalytic | |
FPANIOMK_00089 | 7.1e-172 | tesB | I | Thioesterase-like superfamily | ||
FPANIOMK_00090 | 5.3e-74 | S | Protein of unknown function (DUF3180) | |||
FPANIOMK_00091 | 2.1e-293 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
FPANIOMK_00092 | 2.3e-164 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
FPANIOMK_00093 | 4.5e-100 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
FPANIOMK_00094 | 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 | ||
FPANIOMK_00095 | 2.1e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
FPANIOMK_00096 | 2.3e-212 | 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 | |
FPANIOMK_00097 | 4.5e-261 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
FPANIOMK_00098 | 4.3e-308 | |||||
FPANIOMK_00099 | 1.7e-168 | natA | V | ATPases associated with a variety of cellular activities | ||
FPANIOMK_00100 | 1.3e-232 | epsG | M | Glycosyl transferase family 21 | ||
FPANIOMK_00101 | 4.3e-273 | S | AI-2E family transporter | |||
FPANIOMK_00102 | 4.3e-177 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
FPANIOMK_00103 | 8.1e-205 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
FPANIOMK_00106 | 2.6e-68 | S | Domain of unknown function (DUF4190) | |||
FPANIOMK_00107 | 6.9e-200 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
FPANIOMK_00108 | 4.8e-176 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
FPANIOMK_00110 | 2.6e-11 | |||||
FPANIOMK_00111 | 2.2e-21 | |||||
FPANIOMK_00112 | 1.5e-214 | S | Helix-turn-helix domain | |||
FPANIOMK_00113 | 8e-83 | S | Transcription factor WhiB | |||
FPANIOMK_00114 | 2.1e-103 | parA | D | AAA domain | ||
FPANIOMK_00115 | 4.3e-69 | |||||
FPANIOMK_00116 | 6.2e-25 | |||||
FPANIOMK_00117 | 7.8e-126 | K | Helix-turn-helix domain protein | |||
FPANIOMK_00120 | 0.0 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
FPANIOMK_00121 | 4.9e-47 | V | ABC-2 type transporter | |||
FPANIOMK_00122 | 4.6e-17 | S | Transcription factor WhiB | |||
FPANIOMK_00123 | 1.5e-267 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
FPANIOMK_00124 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
FPANIOMK_00125 | 2.1e-85 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
FPANIOMK_00126 | 1.3e-179 | lacR | K | Transcriptional regulator, LacI family | ||
FPANIOMK_00127 | 8.9e-229 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
FPANIOMK_00128 | 3.9e-119 | K | Transcriptional regulatory protein, C terminal | |||
FPANIOMK_00129 | 4.8e-101 | |||||
FPANIOMK_00130 | 2.1e-178 | V | N-Acetylmuramoyl-L-alanine amidase | |||
FPANIOMK_00131 | 7.4e-109 | ytrE | V | ABC transporter | ||
FPANIOMK_00132 | 6.6e-172 | |||||
FPANIOMK_00134 | 4.7e-220 | vex3 | V | ABC transporter permease | ||
FPANIOMK_00135 | 5.2e-210 | vex1 | V | Efflux ABC transporter, permease protein | ||
FPANIOMK_00136 | 9.9e-112 | vex2 | V | ABC transporter, ATP-binding protein | ||
FPANIOMK_00137 | 8.2e-38 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
FPANIOMK_00138 | 2.2e-196 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
FPANIOMK_00139 | 1.8e-95 | ptpA | 3.1.3.48 | T | low molecular weight | |
FPANIOMK_00140 | 5.1e-127 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
FPANIOMK_00141 | 1.9e-174 | 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 | |
FPANIOMK_00142 | 1e-72 | attW | O | OsmC-like protein | ||
FPANIOMK_00143 | 1.6e-191 | T | Universal stress protein family | |||
FPANIOMK_00144 | 6e-106 | M | NlpC/P60 family | |||
FPANIOMK_00145 | 7.2e-181 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
FPANIOMK_00146 | 4.2e-214 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
FPANIOMK_00147 | 2.6e-39 | |||||
FPANIOMK_00148 | 5.9e-217 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
FPANIOMK_00149 | 1.7e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
FPANIOMK_00150 | 7.6e-09 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00151 | 4.9e-139 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
FPANIOMK_00152 | 1.8e-173 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
FPANIOMK_00153 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
FPANIOMK_00155 | 9.5e-217 | araJ | EGP | Major facilitator Superfamily | ||
FPANIOMK_00156 | 0.0 | S | Domain of unknown function (DUF4037) | |||
FPANIOMK_00157 | 1.6e-111 | S | Protein of unknown function (DUF4125) | |||
FPANIOMK_00158 | 8.5e-131 | |||||
FPANIOMK_00159 | 7.3e-290 | pspC | KT | PspC domain | ||
FPANIOMK_00160 | 2.7e-266 | tcsS3 | KT | PspC domain | ||
FPANIOMK_00161 | 9.2e-126 | degU | K | helix_turn_helix, Lux Regulon | ||
FPANIOMK_00162 | 5.3e-278 | 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 | |
FPANIOMK_00164 | 2.3e-142 | pgl | 3.1.1.31 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
FPANIOMK_00165 | 4.2e-186 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
FPANIOMK_00166 | 0.0 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
FPANIOMK_00167 | 1.8e-95 | |||||
FPANIOMK_00169 | 0.0 | nagLU | 3.1.4.53, 3.2.1.21, 3.2.1.50 | GH3 | G | Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain |
FPANIOMK_00171 | 3e-240 | 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) | |
FPANIOMK_00172 | 0.0 | nucH | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | |
FPANIOMK_00173 | 2.5e-214 | I | Diacylglycerol kinase catalytic domain | |||
FPANIOMK_00174 | 1.7e-151 | arbG | K | CAT RNA binding domain | ||
FPANIOMK_00175 | 0.0 | crr | G | pts system, glucose-specific IIABC component | ||
FPANIOMK_00176 | 6.1e-44 | M | Spy0128-like isopeptide containing domain | |||
FPANIOMK_00177 | 4.6e-74 | M | Spy0128-like isopeptide containing domain | |||
FPANIOMK_00179 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
FPANIOMK_00180 | 2.9e-260 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
FPANIOMK_00181 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
FPANIOMK_00182 | 1.1e-200 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
FPANIOMK_00183 | 2.7e-126 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
FPANIOMK_00185 | 1.2e-106 | |||||
FPANIOMK_00186 | 1e-254 | 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 | ||
FPANIOMK_00187 | 8.5e-232 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
FPANIOMK_00188 | 3.4e-236 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
FPANIOMK_00189 | 4.7e-84 | 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 | ||
FPANIOMK_00190 | 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 | ||
FPANIOMK_00191 | 2.8e-188 | nusA | K | Participates in both transcription termination and antitermination | ||
FPANIOMK_00192 | 1.6e-161 | |||||
FPANIOMK_00193 | 2.5e-70 | L | Transposase and inactivated derivatives | |||
FPANIOMK_00194 | 1.7e-33 | |||||
FPANIOMK_00196 | 1.3e-153 | E | Transglutaminase/protease-like homologues | |||
FPANIOMK_00197 | 0.0 | gcs2 | S | A circularly permuted ATPgrasp | ||
FPANIOMK_00198 | 1.4e-172 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
FPANIOMK_00199 | 0.0 | 3.2.1.52 | GH20 | G | hydrolase family 20, catalytic | |
FPANIOMK_00200 | 2.8e-64 | rplQ | J | Ribosomal protein L17 | ||
FPANIOMK_00201 | 8.9e-184 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
FPANIOMK_00202 | 1.1e-65 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
FPANIOMK_00203 | 3.3e-62 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
FPANIOMK_00204 | 6.5e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
FPANIOMK_00205 | 1.6e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
FPANIOMK_00206 | 3.8e-99 | 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 | |
FPANIOMK_00207 | 1.2e-247 | 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 | ||
FPANIOMK_00208 | 2.7e-63 | rplO | J | binds to the 23S rRNA | ||
FPANIOMK_00209 | 1e-24 | rpmD | J | Ribosomal protein L30p/L7e | ||
FPANIOMK_00210 | 1.5e-100 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
FPANIOMK_00211 | 1.1e-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 | ||
FPANIOMK_00212 | 2.1e-94 | 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 | ||
FPANIOMK_00213 | 4.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
FPANIOMK_00214 | 9.2e-18 | 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 | ||
FPANIOMK_00215 | 2.2e-102 | 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 | ||
FPANIOMK_00216 | 3.5e-52 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
FPANIOMK_00217 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
FPANIOMK_00218 | 3.5e-42 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
FPANIOMK_00219 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
FPANIOMK_00220 | 5.8e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
FPANIOMK_00221 | 7.5e-96 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
FPANIOMK_00222 | 4.3e-56 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
FPANIOMK_00223 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
FPANIOMK_00224 | 4.2e-155 | 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 | ||
FPANIOMK_00225 | 2.6e-46 | 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 | ||
FPANIOMK_00226 | 3.9e-119 | rplD | J | Forms part of the polypeptide exit tunnel | ||
FPANIOMK_00227 | 4.2e-118 | 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 | ||
FPANIOMK_00228 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
FPANIOMK_00229 | 8e-135 | ywiC | S | YwiC-like protein | ||
FPANIOMK_00230 | 8.7e-167 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
FPANIOMK_00231 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
FPANIOMK_00232 | 3.7e-232 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
FPANIOMK_00233 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
FPANIOMK_00234 | 8.8e-68 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
FPANIOMK_00235 | 3.5e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
FPANIOMK_00236 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
FPANIOMK_00237 | 1.8e-120 | |||||
FPANIOMK_00238 | 1.1e-113 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
FPANIOMK_00239 | 3.6e-257 | M | Bacterial capsule synthesis protein PGA_cap | |||
FPANIOMK_00241 | 4.3e-239 | 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 | |
FPANIOMK_00242 | 1.9e-225 | dapC | E | Aminotransferase class I and II | ||
FPANIOMK_00243 | 9e-61 | fdxA | C | 4Fe-4S binding domain | ||
FPANIOMK_00244 | 1.5e-214 | murB | 1.3.1.98 | M | Cell wall formation | |
FPANIOMK_00245 | 1.9e-25 | rpmG | J | Ribosomal protein L33 | ||
FPANIOMK_00249 | 9.2e-51 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
FPANIOMK_00250 | 2.1e-132 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
FPANIOMK_00251 | 1.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
FPANIOMK_00252 | 6.3e-148 | |||||
FPANIOMK_00253 | 2.3e-149 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
FPANIOMK_00254 | 2e-120 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
FPANIOMK_00255 | 3.2e-38 | fmdB | S | Putative regulatory protein | ||
FPANIOMK_00256 | 5.6e-110 | flgA | NO | SAF | ||
FPANIOMK_00257 | 9.6e-42 | |||||
FPANIOMK_00258 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
FPANIOMK_00259 | 2.8e-243 | T | Forkhead associated domain | |||
FPANIOMK_00261 | 1.3e-37 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
FPANIOMK_00262 | 2.1e-88 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
FPANIOMK_00263 | 4.4e-183 | xynB2 | 1.1.1.169 | E | lipolytic protein G-D-S-L family | |
FPANIOMK_00264 | 0.0 | guxA1 | 3.2.1.18, 3.2.1.91 | GH33,GH6 | G | BNR repeat-like domain |
FPANIOMK_00266 | 8.8e-222 | pbuO | S | Permease family | ||
FPANIOMK_00267 | 1.2e-11 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
FPANIOMK_00268 | 2.7e-160 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
FPANIOMK_00269 | 3.6e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
FPANIOMK_00270 | 1.8e-179 | pstA | P | Phosphate transport system permease | ||
FPANIOMK_00271 | 2.5e-170 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
FPANIOMK_00272 | 3e-172 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
FPANIOMK_00273 | 1.3e-128 | KT | Transcriptional regulatory protein, C terminal | |||
FPANIOMK_00274 | 8.5e-246 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
FPANIOMK_00275 | 8.7e-125 | 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 | |
FPANIOMK_00276 | 1.7e-240 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
FPANIOMK_00277 | 9.7e-109 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
FPANIOMK_00278 | 5.6e-245 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00279 | 3.3e-219 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
FPANIOMK_00280 | 6.8e-171 | L | Excalibur calcium-binding domain | |||
FPANIOMK_00281 | 3.2e-269 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
FPANIOMK_00282 | 2.6e-51 | D | nuclear chromosome segregation | |||
FPANIOMK_00283 | 8e-128 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
FPANIOMK_00284 | 6.5e-145 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
FPANIOMK_00285 | 3.9e-187 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
FPANIOMK_00286 | 0.0 | yegQ | O | Peptidase family U32 C-terminal domain | ||
FPANIOMK_00287 | 8.1e-108 | L | Transposase and inactivated derivatives IS30 family | |||
FPANIOMK_00288 | 1.5e-95 | L | Transposase and inactivated derivatives IS30 family | |||
FPANIOMK_00289 | 4.6e-168 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
FPANIOMK_00290 | 2.2e-41 | nrdH | O | Glutaredoxin | ||
FPANIOMK_00291 | 1.5e-98 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
FPANIOMK_00292 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
FPANIOMK_00293 | 1.4e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
FPANIOMK_00294 | 5e-73 | megL | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
FPANIOMK_00295 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
FPANIOMK_00296 | 1e-91 | lemA | S | LemA family | ||
FPANIOMK_00297 | 7.2e-116 | xylR | K | purine nucleotide biosynthetic process | ||
FPANIOMK_00298 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
FPANIOMK_00299 | 3e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
FPANIOMK_00300 | 4.9e-117 | |||||
FPANIOMK_00301 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
FPANIOMK_00303 | 1.9e-161 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
FPANIOMK_00304 | 3.8e-99 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
FPANIOMK_00305 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
FPANIOMK_00306 | 7.2e-308 | pccB | I | Carboxyl transferase domain | ||
FPANIOMK_00307 | 0.0 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
FPANIOMK_00308 | 4.2e-93 | bioY | S | BioY family | ||
FPANIOMK_00309 | 1.1e-150 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
FPANIOMK_00310 | 0.0 | |||||
FPANIOMK_00311 | 2.3e-145 | QT | PucR C-terminal helix-turn-helix domain | |||
FPANIOMK_00312 | 9.5e-132 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
FPANIOMK_00313 | 8.7e-50 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
FPANIOMK_00314 | 1.5e-283 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
FPANIOMK_00315 | 2.7e-166 | 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 | ||
FPANIOMK_00316 | 0.0 | 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 | |
FPANIOMK_00317 | 1.4e-150 | 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 | ||
FPANIOMK_00318 | 4.6e-62 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
FPANIOMK_00319 | 8.3e-29 | 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 | ||
FPANIOMK_00321 | 6e-146 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
FPANIOMK_00322 | 4.1e-208 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
FPANIOMK_00324 | 9.2e-36 | |||||
FPANIOMK_00325 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
FPANIOMK_00326 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
FPANIOMK_00327 | 5.2e-92 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
FPANIOMK_00329 | 1.3e-102 | mntP | P | Probably functions as a manganese efflux pump | ||
FPANIOMK_00330 | 1.4e-125 | |||||
FPANIOMK_00331 | 2e-135 | KT | Transcriptional regulatory protein, C terminal | |||
FPANIOMK_00332 | 1.9e-126 | 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 | |
FPANIOMK_00333 | 4.3e-294 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
FPANIOMK_00334 | 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 | |
FPANIOMK_00335 | 0.0 | S | domain protein | |||
FPANIOMK_00336 | 4.7e-73 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
FPANIOMK_00337 | 9.9e-83 | lrp_3 | K | helix_turn_helix ASNC type | ||
FPANIOMK_00338 | 4.7e-235 | E | Aminotransferase class I and II | |||
FPANIOMK_00339 | 4.7e-304 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
FPANIOMK_00340 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
FPANIOMK_00341 | 3.3e-52 | S | Protein of unknown function (DUF2469) | |||
FPANIOMK_00342 | 3e-198 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
FPANIOMK_00343 | 1.4e-286 | gatB | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
FPANIOMK_00344 | 2.4e-289 | gatA | 6.3.5.6, 6.3.5.7 | F | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
FPANIOMK_00345 | 6.2e-48 | 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) | |
FPANIOMK_00346 | 4.8e-15 | V | ABC transporter | |||
FPANIOMK_00347 | 2.8e-61 | V | ABC transporter | |||
FPANIOMK_00348 | 2.3e-60 | V | ABC transporter | |||
FPANIOMK_00349 | 6.9e-156 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
FPANIOMK_00350 | 5.9e-129 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
FPANIOMK_00351 | 1.3e-214 | rmuC | S | RmuC family | ||
FPANIOMK_00352 | 1.4e-42 | csoR | S | Metal-sensitive transcriptional repressor | ||
FPANIOMK_00353 | 0.0 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
FPANIOMK_00354 | 0.0 | ubiB | S | ABC1 family | ||
FPANIOMK_00355 | 3.5e-19 | S | granule-associated protein | |||
FPANIOMK_00356 | 7.5e-143 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
FPANIOMK_00357 | 4e-279 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
FPANIOMK_00358 | 4.9e-257 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
FPANIOMK_00359 | 2.4e-251 | dinF | V | MatE | ||
FPANIOMK_00360 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
FPANIOMK_00361 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
FPANIOMK_00362 | 1.3e-219 | amt | U | Ammonium Transporter Family | ||
FPANIOMK_00363 | 2e-201 | 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) | ||
FPANIOMK_00365 | 1.2e-116 | icaR | K | Bacterial regulatory proteins, tetR family | ||
FPANIOMK_00366 | 6.6e-198 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
FPANIOMK_00367 | 0.0 | S | Glycosyl hydrolases related to GH101 family, GH129 | |||
FPANIOMK_00368 | 3.5e-304 | pepD | E | Peptidase family C69 | ||
FPANIOMK_00370 | 1.4e-86 | XK26_04485 | P | Cobalt transport protein | ||
FPANIOMK_00371 | 3.4e-82 | |||||
FPANIOMK_00372 | 0.0 | V | ABC transporter transmembrane region | |||
FPANIOMK_00373 | 5.9e-300 | V | ABC transporter, ATP-binding protein | |||
FPANIOMK_00374 | 1.3e-81 | K | Winged helix DNA-binding domain | |||
FPANIOMK_00375 | 3e-73 | E | IrrE N-terminal-like domain | |||
FPANIOMK_00377 | 2.1e-162 | S | Sucrose-6F-phosphate phosphohydrolase | |||
FPANIOMK_00378 | 2.7e-241 | S | Putative ABC-transporter type IV | |||
FPANIOMK_00379 | 1.6e-80 | |||||
FPANIOMK_00380 | 8.1e-35 | Q | phosphatase activity | |||
FPANIOMK_00381 | 6.8e-294 | bglA | 3.2.1.86 | GT1 | G | Glycosyl hydrolase family 1 |
FPANIOMK_00382 | 7.5e-39 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
FPANIOMK_00383 | 1.2e-48 | celA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
FPANIOMK_00384 | 2.1e-249 | gmuC | 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 | ||
FPANIOMK_00385 | 4.6e-67 | S | haloacid dehalogenase-like hydrolase | |||
FPANIOMK_00386 | 3.6e-131 | yydK | K | UTRA | ||
FPANIOMK_00387 | 1.3e-70 | S | FMN_bind | |||
FPANIOMK_00388 | 5.7e-149 | macB | V | ABC transporter, ATP-binding protein | ||
FPANIOMK_00389 | 2.6e-204 | Z012_06715 | V | FtsX-like permease family | ||
FPANIOMK_00390 | 4.8e-222 | macB_2 | V | ABC transporter permease | ||
FPANIOMK_00391 | 9.2e-234 | S | Predicted membrane protein (DUF2318) | |||
FPANIOMK_00392 | 1.8e-106 | tpd | P | Fe2+ transport protein | ||
FPANIOMK_00393 | 4.6e-308 | efeU_1 | P | Iron permease FTR1 family | ||
FPANIOMK_00394 | 5.9e-22 | G | MFS/sugar transport protein | |||
FPANIOMK_00395 | 1.1e-200 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
FPANIOMK_00396 | 1.2e-56 | S | Fic/DOC family | |||
FPANIOMK_00397 | 1.3e-32 | S | Fic/DOC family | |||
FPANIOMK_00398 | 3.6e-291 | 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) | |
FPANIOMK_00399 | 5e-38 | ptsH | G | PTS HPr component phosphorylation site | ||
FPANIOMK_00400 | 4.4e-200 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_00401 | 1.6e-211 | holB | 2.7.7.7 | L | DNA polymerase III | |
FPANIOMK_00402 | 1.1e-117 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
FPANIOMK_00403 | 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 | |
FPANIOMK_00404 | 2.3e-188 | 3.6.1.27 | I | PAP2 superfamily | ||
FPANIOMK_00405 | 0.0 | vpr | M | PA domain | ||
FPANIOMK_00406 | 2.7e-123 | yplQ | S | Haemolysin-III related | ||
FPANIOMK_00407 | 9.3e-233 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
FPANIOMK_00408 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
FPANIOMK_00409 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
FPANIOMK_00410 | 3.9e-278 | S | Calcineurin-like phosphoesterase | |||
FPANIOMK_00411 | 4.3e-14 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
FPANIOMK_00412 | 6.6e-281 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
FPANIOMK_00413 | 1.7e-116 | |||||
FPANIOMK_00414 | 3.2e-211 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
FPANIOMK_00415 | 1.8e-96 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
FPANIOMK_00416 | 5.3e-136 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
FPANIOMK_00417 | 6.7e-110 | 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 | ||
FPANIOMK_00418 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
FPANIOMK_00419 | 2.4e-214 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
FPANIOMK_00420 | 3.1e-57 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
FPANIOMK_00421 | 3.2e-41 | S | Protein of unknown function (DUF4244) | |||
FPANIOMK_00422 | 3.2e-15 | gspF | NU | Type II secretion system (T2SS), protein F | ||
FPANIOMK_00423 | 1.8e-14 | gspF | NU | Type II secretion system (T2SS), protein F | ||
FPANIOMK_00424 | 1.3e-120 | U | Type ii secretion system | |||
FPANIOMK_00425 | 3.4e-191 | cpaF | U | Type II IV secretion system protein | ||
FPANIOMK_00426 | 1.3e-151 | cpaE | D | bacterial-type flagellum organization | ||
FPANIOMK_00428 | 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) | |
FPANIOMK_00429 | 5.3e-200 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
FPANIOMK_00430 | 5.9e-92 | |||||
FPANIOMK_00432 | 9.7e-29 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
FPANIOMK_00433 | 1.7e-209 | S | Glycosyltransferase, group 2 family protein | |||
FPANIOMK_00434 | 5.2e-262 | |||||
FPANIOMK_00436 | 8.7e-27 | thiS | 2.8.1.10 | H | ThiS family | |
FPANIOMK_00437 | 1.9e-164 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
FPANIOMK_00438 | 2.2e-176 | S | Psort location Cytoplasmic, score 8.87 | |||
FPANIOMK_00439 | 5.4e-106 | S | Psort location Cytoplasmic, score 8.87 | |||
FPANIOMK_00440 | 0.0 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
FPANIOMK_00441 | 3.9e-249 | V | ABC transporter permease | |||
FPANIOMK_00442 | 1.6e-185 | V | ABC transporter | |||
FPANIOMK_00443 | 7.9e-137 | T | HD domain | |||
FPANIOMK_00444 | 3e-164 | S | Glutamine amidotransferase domain | |||
FPANIOMK_00446 | 0.0 | kup | P | Transport of potassium into the cell | ||
FPANIOMK_00447 | 5.9e-185 | tatD | L | TatD related DNase | ||
FPANIOMK_00448 | 4.2e-275 | xylR | 5.3.1.12 | G | MFS/sugar transport protein | |
FPANIOMK_00450 | 8.9e-87 | K | Transcriptional regulator | |||
FPANIOMK_00451 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
FPANIOMK_00452 | 1.6e-130 | |||||
FPANIOMK_00453 | 8.6e-59 | |||||
FPANIOMK_00454 | 3.1e-168 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
FPANIOMK_00455 | 2.7e-126 | dedA | S | SNARE associated Golgi protein | ||
FPANIOMK_00457 | 4.7e-140 | S | HAD hydrolase, family IA, variant 3 | |||
FPANIOMK_00458 | 0.0 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR Asp-box repeat | |
FPANIOMK_00459 | 0.0 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR repeat-like domain | |
FPANIOMK_00460 | 6.8e-87 | hspR | K | transcriptional regulator, MerR family | ||
FPANIOMK_00461 | 2.4e-173 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
FPANIOMK_00462 | 1.4e-58 | 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 | ||
FPANIOMK_00463 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
FPANIOMK_00464 | 0.0 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
FPANIOMK_00465 | 2.9e-190 | K | Psort location Cytoplasmic, score | |||
FPANIOMK_00467 | 1.8e-138 | G | Phosphoglycerate mutase family | |||
FPANIOMK_00468 | 8e-70 | S | Protein of unknown function (DUF4235) | |||
FPANIOMK_00469 | 2.3e-142 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
FPANIOMK_00470 | 1.1e-45 | |||||
FPANIOMK_00471 | 8.8e-31 | plyA3 | M | Parallel beta-helix repeats | ||
FPANIOMK_00472 | 7.1e-31 | plyA3 | 3.2.1.18 | GH33 | M | Parallel beta-helix repeats |
FPANIOMK_00473 | 0.0 | plyA3 | M | Parallel beta-helix repeats | ||
FPANIOMK_00474 | 5.5e-259 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
FPANIOMK_00475 | 9.3e-164 | |||||
FPANIOMK_00476 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
FPANIOMK_00477 | 4.3e-140 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
FPANIOMK_00478 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
FPANIOMK_00479 | 8.5e-273 | 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 | |
FPANIOMK_00480 | 7.8e-43 | 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 | |
FPANIOMK_00481 | 3.6e-171 | S | Endonuclease/Exonuclease/phosphatase family | |||
FPANIOMK_00484 | 1.4e-181 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
FPANIOMK_00485 | 1.3e-254 | cdr | OP | Sulfurtransferase TusA | ||
FPANIOMK_00486 | 7.5e-149 | moeB | 2.7.7.80 | H | ThiF family | |
FPANIOMK_00487 | 1.6e-132 | tmp1 | S | Domain of unknown function (DUF4391) | ||
FPANIOMK_00488 | 2.3e-37 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
FPANIOMK_00489 | 2.9e-229 | aspB | E | Aminotransferase class-V | ||
FPANIOMK_00490 | 2.5e-101 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
FPANIOMK_00491 | 3.6e-271 | S | zinc finger | |||
FPANIOMK_00492 | 1.2e-123 | def | 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 | |
FPANIOMK_00493 | 1.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
FPANIOMK_00494 | 4.3e-292 | O | Subtilase family | |||
FPANIOMK_00495 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
FPANIOMK_00496 | 0.0 | rnj | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
FPANIOMK_00497 | 1.9e-161 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
FPANIOMK_00498 | 1e-132 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
FPANIOMK_00499 | 1.4e-59 | L | Transposase | |||
FPANIOMK_00500 | 6.4e-24 | relB | L | RelB antitoxin | ||
FPANIOMK_00501 | 2.7e-10 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
FPANIOMK_00502 | 6.5e-43 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
FPANIOMK_00503 | 2.9e-66 | gsiA | P | ATPase activity | ||
FPANIOMK_00504 | 1.3e-257 | G | Major Facilitator Superfamily | |||
FPANIOMK_00505 | 8.6e-159 | K | -acetyltransferase | |||
FPANIOMK_00506 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
FPANIOMK_00507 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
FPANIOMK_00508 | 7.5e-269 | KLT | Protein tyrosine kinase | |||
FPANIOMK_00509 | 0.0 | S | Fibronectin type 3 domain | |||
FPANIOMK_00510 | 2.4e-229 | S | ATPase family associated with various cellular activities (AAA) | |||
FPANIOMK_00511 | 6.6e-227 | S | Protein of unknown function DUF58 | |||
FPANIOMK_00512 | 0.0 | E | Transglutaminase-like superfamily | |||
FPANIOMK_00513 | 2e-166 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
FPANIOMK_00514 | 2.8e-68 | B | Belongs to the OprB family | |||
FPANIOMK_00515 | 7.2e-95 | T | Forkhead associated domain | |||
FPANIOMK_00516 | 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 | |
FPANIOMK_00517 | 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 | |
FPANIOMK_00518 | 9.6e-102 | |||||
FPANIOMK_00519 | 1.2e-182 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
FPANIOMK_00520 | 8.1e-29 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | xyloglucan:xyloglucosyl transferase activity |
FPANIOMK_00521 | 1.2e-42 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | Putative cell wall binding repeat |
FPANIOMK_00523 | 6.3e-122 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
FPANIOMK_00525 | 3.9e-73 | |||||
FPANIOMK_00526 | 1e-251 | S | UPF0210 protein | |||
FPANIOMK_00527 | 4.2e-43 | gcvR | T | Belongs to the UPF0237 family | ||
FPANIOMK_00528 | 8.6e-243 | EGP | Sugar (and other) transporter | |||
FPANIOMK_00529 | 9.9e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
FPANIOMK_00530 | 2.8e-251 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
FPANIOMK_00531 | 3.1e-139 | glpR | K | DeoR C terminal sensor domain | ||
FPANIOMK_00532 | 6.7e-227 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
FPANIOMK_00533 | 1.5e-216 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
FPANIOMK_00534 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
FPANIOMK_00535 | 1.6e-134 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
FPANIOMK_00536 | 6.4e-119 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
FPANIOMK_00537 | 2e-191 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
FPANIOMK_00538 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
FPANIOMK_00539 | 2e-239 | S | Uncharacterized conserved protein (DUF2183) | |||
FPANIOMK_00540 | 3.7e-72 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
FPANIOMK_00541 | 0.0 | enhA_2 | S | L,D-transpeptidase catalytic domain | ||
FPANIOMK_00542 | 2.4e-08 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
FPANIOMK_00543 | 2e-160 | mhpC | I | Alpha/beta hydrolase family | ||
FPANIOMK_00544 | 4.8e-119 | F | Domain of unknown function (DUF4916) | |||
FPANIOMK_00545 | 1.5e-59 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
FPANIOMK_00546 | 1.3e-179 | S | G5 | |||
FPANIOMK_00547 | 4.3e-225 | |||||
FPANIOMK_00548 | 1.8e-306 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00549 | 2.5e-226 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
FPANIOMK_00550 | 2.1e-134 | L | Protein of unknown function (DUF1524) | |||
FPANIOMK_00551 | 2.9e-170 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
FPANIOMK_00552 | 9.3e-11 | 3.2.1.14 | GH18 | EM | Domain of unknown function (DUF5011) | |
FPANIOMK_00553 | 2.3e-199 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_00554 | 2.5e-103 | G | Glycosyl hydrolases family 43 | |||
FPANIOMK_00555 | 2.2e-174 | G | Glycosyl hydrolases family 43 | |||
FPANIOMK_00558 | 3.7e-111 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
FPANIOMK_00559 | 6.9e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
FPANIOMK_00560 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
FPANIOMK_00561 | 4.4e-208 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_00562 | 2.5e-132 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
FPANIOMK_00563 | 1.8e-158 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
FPANIOMK_00564 | 5.6e-62 | 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 | ||
FPANIOMK_00565 | 3.3e-129 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
FPANIOMK_00566 | 3.1e-172 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
FPANIOMK_00567 | 3.2e-294 | 2.7.1.53 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
FPANIOMK_00568 | 8.8e-213 | gatC | G | PTS system sugar-specific permease component | ||
FPANIOMK_00569 | 1.4e-173 | K | Putative sugar-binding domain | |||
FPANIOMK_00570 | 0.0 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_00571 | 3.9e-276 | abcT3 | P | ATPases associated with a variety of cellular activities | ||
FPANIOMK_00572 | 0.0 | mgtA | 3.6.3.2 | P | Cation transporting ATPase, C-terminus | |
FPANIOMK_00573 | 3e-120 | mgtC | S | MgtC family | ||
FPANIOMK_00575 | 5.8e-200 | |||||
FPANIOMK_00577 | 1.5e-190 | |||||
FPANIOMK_00578 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
FPANIOMK_00581 | 1.1e-173 | S | Auxin Efflux Carrier | |||
FPANIOMK_00582 | 3.7e-117 | 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 | |
FPANIOMK_00583 | 2.1e-134 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
FPANIOMK_00584 | 4.4e-247 | 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 | |
FPANIOMK_00586 | 7.6e-92 | ilvN | 2.2.1.6 | E | ACT domain | |
FPANIOMK_00587 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
FPANIOMK_00588 | 2.3e-139 | 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 | |
FPANIOMK_00589 | 2.3e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
FPANIOMK_00590 | 2.3e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
FPANIOMK_00591 | 3.6e-107 | |||||
FPANIOMK_00592 | 1.7e-81 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
FPANIOMK_00593 | 2e-58 | S | Protein of unknown function (DUF3039) | |||
FPANIOMK_00594 | 0.0 | yjjK | S | ABC transporter | ||
FPANIOMK_00595 | 2.3e-136 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
FPANIOMK_00596 | 0.0 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FPANIOMK_00597 | 1.4e-164 | P | Cation efflux family | |||
FPANIOMK_00598 | 2.3e-269 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
FPANIOMK_00599 | 1.9e-222 | S | Endonuclease/Exonuclease/phosphatase family | |||
FPANIOMK_00600 | 1.3e-93 | argO | S | LysE type translocator | ||
FPANIOMK_00601 | 1.5e-294 | ydfD | EK | Alanine-glyoxylate amino-transferase | ||
FPANIOMK_00602 | 1e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
FPANIOMK_00603 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
FPANIOMK_00604 | 6.4e-108 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
FPANIOMK_00605 | 1.4e-165 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
FPANIOMK_00606 | 8.9e-83 | hsp20 | O | Hsp20/alpha crystallin family | ||
FPANIOMK_00607 | 6.3e-108 | XK27_02070 | S | Nitroreductase family | ||
FPANIOMK_00608 | 6.4e-120 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
FPANIOMK_00609 | 1.3e-248 | U | Sodium:dicarboxylate symporter family | |||
FPANIOMK_00610 | 0.0 | |||||
FPANIOMK_00613 | 4.5e-220 | steT | E | amino acid | ||
FPANIOMK_00614 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
FPANIOMK_00615 | 1.4e-29 | rpmB | J | Ribosomal L28 family | ||
FPANIOMK_00616 | 6.5e-201 | yegV | G | pfkB family carbohydrate kinase | ||
FPANIOMK_00618 | 1.5e-242 | yxiO | S | Vacuole effluxer Atg22 like | ||
FPANIOMK_00619 | 5.9e-132 | K | helix_turn_helix, mercury resistance | |||
FPANIOMK_00620 | 2.6e-17 | T | Toxic component of a toxin-antitoxin (TA) module | |||
FPANIOMK_00621 | 3.7e-54 | relB | L | RelB antitoxin | ||
FPANIOMK_00622 | 9.6e-236 | K | Helix-turn-helix XRE-family like proteins | |||
FPANIOMK_00623 | 1.3e-131 | tam | 2.1.1.144, 2.1.1.197 | S | Methyltransferase domain | |
FPANIOMK_00628 | 1.7e-32 | |||||
FPANIOMK_00629 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
FPANIOMK_00630 | 2.1e-42 | K | Transcriptional regulator | |||
FPANIOMK_00632 | 3.2e-60 | M | Belongs to the glycosyl hydrolase 28 family | |||
FPANIOMK_00633 | 4.2e-233 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
FPANIOMK_00634 | 4.3e-73 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
FPANIOMK_00635 | 1.7e-119 | K | Bacterial regulatory proteins, tetR family | |||
FPANIOMK_00636 | 2.7e-132 | M | Mechanosensitive ion channel | |||
FPANIOMK_00637 | 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 | ||
FPANIOMK_00638 | 1.3e-156 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
FPANIOMK_00639 | 4.1e-62 | S | Domain of unknown function (DUF4854) | |||
FPANIOMK_00640 | 1e-210 | 3.4.22.70 | M | Sortase family | ||
FPANIOMK_00641 | 2e-278 | M | LPXTG cell wall anchor motif | |||
FPANIOMK_00642 | 0.0 | inlJ | M | domain protein | ||
FPANIOMK_00643 | 3.6e-53 | acyP | 3.6.1.7 | C | Acylphosphatase | |
FPANIOMK_00644 | 2.2e-148 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
FPANIOMK_00645 | 3.5e-185 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FPANIOMK_00646 | 3e-129 | M | Protein of unknown function (DUF3152) | |||
FPANIOMK_00647 | 3.7e-131 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
FPANIOMK_00649 | 1.6e-65 | E | Domain of unknown function (DUF5011) | |||
FPANIOMK_00650 | 1e-46 | S | Parallel beta-helix repeats | |||
FPANIOMK_00651 | 1.3e-14 | S | Parallel beta-helix repeats | |||
FPANIOMK_00652 | 1.9e-69 | rplI | J | Binds to the 23S rRNA | ||
FPANIOMK_00653 | 2e-36 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
FPANIOMK_00654 | 1.1e-79 | ssb1 | L | Single-stranded DNA-binding protein | ||
FPANIOMK_00655 | 6.1e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
FPANIOMK_00656 | 2.5e-42 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
FPANIOMK_00657 | 2.8e-116 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
FPANIOMK_00658 | 1.8e-117 | |||||
FPANIOMK_00659 | 0.0 | ftsK | 2.7.11.1, 2.7.7.7, 3.4.21.110, 4.2.1.2 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |
FPANIOMK_00660 | 6.9e-192 | 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) | |
FPANIOMK_00661 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolase 101 beta sandwich domain | |
FPANIOMK_00662 | 7.5e-202 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
FPANIOMK_00663 | 3.4e-219 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
FPANIOMK_00664 | 2.5e-178 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
FPANIOMK_00665 | 2.8e-173 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
FPANIOMK_00666 | 1.8e-116 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
FPANIOMK_00667 | 4.7e-32 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
FPANIOMK_00669 | 2e-230 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
FPANIOMK_00670 | 4.1e-201 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
FPANIOMK_00671 | 1.1e-298 | 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 | ||
FPANIOMK_00672 | 2.7e-213 | K | Psort location Cytoplasmic, score | |||
FPANIOMK_00673 | 3.1e-40 | rpmA | J | Ribosomal L27 protein | ||
FPANIOMK_00674 | 3.2e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
FPANIOMK_00675 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
FPANIOMK_00676 | 1.1e-239 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
FPANIOMK_00677 | 2.2e-168 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
FPANIOMK_00678 | 3.3e-256 | V | Efflux ABC transporter, permease protein | |||
FPANIOMK_00679 | 4.1e-164 | V | ATPases associated with a variety of cellular activities | |||
FPANIOMK_00680 | 6.8e-57 | |||||
FPANIOMK_00681 | 1.6e-64 | |||||
FPANIOMK_00682 | 1.8e-278 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
FPANIOMK_00683 | 3.5e-188 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
FPANIOMK_00684 | 5.2e-240 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
FPANIOMK_00685 | 1.1e-289 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
FPANIOMK_00686 | 1.9e-81 | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
FPANIOMK_00687 | 8.8e-306 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
FPANIOMK_00688 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
FPANIOMK_00689 | 3.1e-198 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | ||
FPANIOMK_00690 | 5.2e-63 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
FPANIOMK_00691 | 2.2e-156 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
FPANIOMK_00692 | 5.4e-160 | neo | 2.7.1.87, 2.7.1.95 | F | Phosphotransferase enzyme family | |
FPANIOMK_00693 | 8.2e-66 | L | Integrase core domain | |||
FPANIOMK_00694 | 3.5e-41 | 2.3.1.39 | IQ | [acyl-carrier-protein] S-malonyltransferase activity | ||
FPANIOMK_00695 | 5e-266 | EGP | Major Facilitator Superfamily | |||
FPANIOMK_00696 | 2.9e-243 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
FPANIOMK_00697 | 5.5e-55 | L | HNH endonuclease | |||
FPANIOMK_00698 | 0.0 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
FPANIOMK_00699 | 0.0 | yvnB | 3.1.4.53 | S | Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes | |
FPANIOMK_00700 | 1.6e-105 | L | Transposase | |||
FPANIOMK_00701 | 2.1e-41 | XAC3035 | O | Glutaredoxin | ||
FPANIOMK_00702 | 8.1e-150 | S | Virulence factor BrkB | |||
FPANIOMK_00703 | 1.3e-99 | bcp | 1.11.1.15 | O | Redoxin | |
FPANIOMK_00704 | 2.4e-37 | E | ABC transporter | |||
FPANIOMK_00705 | 3e-116 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
FPANIOMK_00706 | 8.6e-84 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
FPANIOMK_00707 | 0.0 | V | FtsX-like permease family | |||
FPANIOMK_00708 | 2.6e-129 | V | ABC transporter | |||
FPANIOMK_00709 | 7e-101 | K | Transcriptional regulator C-terminal region | |||
FPANIOMK_00710 | 9.6e-275 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
FPANIOMK_00711 | 0.0 | lacZ | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
FPANIOMK_00712 | 8.8e-184 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein of unknown function (DUF559) | |
FPANIOMK_00713 | 1.4e-127 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
FPANIOMK_00714 | 1.2e-41 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
FPANIOMK_00715 | 2.6e-180 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
FPANIOMK_00716 | 2.9e-254 | yhjE | EGP | Sugar (and other) transporter | ||
FPANIOMK_00717 | 7e-298 | scrT | G | Transporter major facilitator family protein | ||
FPANIOMK_00718 | 4.8e-78 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
FPANIOMK_00719 | 8.4e-193 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_00720 | 1.5e-59 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
FPANIOMK_00721 | 3.1e-162 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
FPANIOMK_00722 | 8.3e-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 | |
FPANIOMK_00723 | 3.3e-200 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
FPANIOMK_00724 | 3.1e-245 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
FPANIOMK_00725 | 1.5e-48 | |||||
FPANIOMK_00726 | 3.9e-116 | ltrBE1 | U | Relaxase/Mobilisation nuclease domain | ||
FPANIOMK_00727 | 3.1e-33 | S | Bacterial mobilisation protein (MobC) | |||
FPANIOMK_00728 | 1.2e-83 | S | GyrI-like small molecule binding domain | |||
FPANIOMK_00729 | 5.7e-41 | S | Polyketide cyclase / dehydrase and lipid transport | |||
FPANIOMK_00730 | 5.2e-69 | K | FR47-like protein | |||
FPANIOMK_00731 | 2.1e-80 | S | Nucleotidyltransferase domain | |||
FPANIOMK_00732 | 4.7e-196 | |||||
FPANIOMK_00733 | 1.7e-84 | S | Protein of unknown function DUF262 | |||
FPANIOMK_00734 | 8.5e-63 | S | Protein of unknown function DUF262 | |||
FPANIOMK_00736 | 3.1e-170 | htpX | O | Belongs to the peptidase M48B family | ||
FPANIOMK_00737 | 5e-273 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
FPANIOMK_00738 | 0.0 | cadA | P | E1-E2 ATPase | ||
FPANIOMK_00739 | 2.3e-241 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
FPANIOMK_00740 | 9.3e-258 | 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) | |
FPANIOMK_00742 | 3.8e-84 | yjcF | Q | Acetyltransferase (GNAT) domain | ||
FPANIOMK_00743 | 7.6e-157 | I | Serine aminopeptidase, S33 | |||
FPANIOMK_00744 | 9.3e-53 | ybjQ | S | Putative heavy-metal-binding | ||
FPANIOMK_00745 | 5.2e-39 | D | DivIVA domain protein | |||
FPANIOMK_00746 | 1.7e-90 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
FPANIOMK_00747 | 0.0 | KL | Domain of unknown function (DUF3427) | |||
FPANIOMK_00749 | 6e-196 | 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 | |
FPANIOMK_00751 | 2.6e-103 | |||||
FPANIOMK_00752 | 6.2e-166 | yicL | EG | EamA-like transporter family | ||
FPANIOMK_00753 | 4.6e-207 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
FPANIOMK_00754 | 0.0 | pip | S | YhgE Pip domain protein | ||
FPANIOMK_00755 | 0.0 | pip | S | YhgE Pip domain protein | ||
FPANIOMK_00756 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
FPANIOMK_00757 | 1e-130 | fhaA | T | Protein of unknown function (DUF2662) | ||
FPANIOMK_00758 | 1.9e-92 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
FPANIOMK_00759 | 5.3e-258 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
FPANIOMK_00760 | 2.8e-266 | rodA | D | Belongs to the SEDS family | ||
FPANIOMK_00761 | 3.4e-264 | pbpA | M | penicillin-binding protein | ||
FPANIOMK_00762 | 2e-183 | T | Protein tyrosine kinase | |||
FPANIOMK_00763 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
FPANIOMK_00764 | 3.4e-120 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
FPANIOMK_00765 | 6.3e-232 | srtA | 3.4.22.70 | M | Sortase family | |
FPANIOMK_00766 | 7.9e-143 | S | Bacterial protein of unknown function (DUF881) | |||
FPANIOMK_00767 | 2.6e-71 | crgA | D | Involved in cell division | ||
FPANIOMK_00768 | 1.4e-256 | L | ribosomal rna small subunit methyltransferase | |||
FPANIOMK_00769 | 1.3e-120 | L | HTH-like domain | |||
FPANIOMK_00770 | 1.9e-144 | gluP | 3.4.21.105 | S | Rhomboid family | |
FPANIOMK_00771 | 3.4e-35 | |||||
FPANIOMK_00772 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
FPANIOMK_00773 | 2e-73 | I | Sterol carrier protein | |||
FPANIOMK_00774 | 8.7e-46 | L | Transposase | |||
FPANIOMK_00775 | 2.5e-52 | L | IstB-like ATP binding protein | |||
FPANIOMK_00776 | 1.1e-42 | tnp7109-21 | L | Integrase core domain | ||
FPANIOMK_00777 | 0.0 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
FPANIOMK_00778 | 3.5e-12 | |||||
FPANIOMK_00779 | 3.4e-17 | yccF | S | Inner membrane component domain | ||
FPANIOMK_00780 | 8.8e-259 | S | Domain of unknown function (DUF4143) | |||
FPANIOMK_00781 | 1.9e-65 | L | Transposase and inactivated derivatives IS30 family | |||
FPANIOMK_00782 | 2.8e-193 | M | Glycosyltransferase like family 2 | |||
FPANIOMK_00783 | 2.3e-53 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
FPANIOMK_00785 | 1.1e-152 | IQ | KR domain | |||
FPANIOMK_00786 | 1.7e-34 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
FPANIOMK_00787 | 1.6e-17 | 4.2.1.68 | M | carboxylic acid catabolic process | ||
FPANIOMK_00788 | 1.4e-184 | K | Bacterial regulatory proteins, lacI family | |||
FPANIOMK_00791 | 6.9e-118 | cyaA | 4.6.1.1 | S | CYTH | |
FPANIOMK_00792 | 3.8e-163 | trxA2 | O | Tetratricopeptide repeat | ||
FPANIOMK_00793 | 7.9e-180 | |||||
FPANIOMK_00794 | 7.1e-187 | |||||
FPANIOMK_00795 | 8.3e-166 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
FPANIOMK_00796 | 6.1e-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 | ||
FPANIOMK_00797 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
FPANIOMK_00798 | 2e-124 | |||||
FPANIOMK_00799 | 8.1e-131 | K | Bacterial regulatory proteins, tetR family | |||
FPANIOMK_00800 | 1.6e-225 | G | Transmembrane secretion effector | |||
FPANIOMK_00801 | 9.8e-255 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
FPANIOMK_00802 | 3.6e-221 | pyrD | 1.3.1.14 | F | Dihydroorotate dehydrogenase | |
FPANIOMK_00803 | 1.9e-182 | S | CAAX protease self-immunity | |||
FPANIOMK_00805 | 0.0 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
FPANIOMK_00806 | 3.8e-133 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
FPANIOMK_00807 | 2.2e-273 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
FPANIOMK_00808 | 2.8e-138 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
FPANIOMK_00809 | 1.7e-251 | S | Calcineurin-like phosphoesterase | |||
FPANIOMK_00812 | 4.7e-64 | S | Domain of unknown function (DUF4143) | |||
FPANIOMK_00813 | 1.4e-95 | S | Domain of unknown function (DUF4143) | |||
FPANIOMK_00814 | 1.8e-297 | gltX | 6.1.1.17 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
FPANIOMK_00816 | 3.1e-124 | S | HAD hydrolase, family IA, variant 3 | |||
FPANIOMK_00817 | 8.6e-201 | P | NMT1/THI5 like | |||
FPANIOMK_00818 | 1.7e-137 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
FPANIOMK_00819 | 4.4e-145 | |||||
FPANIOMK_00820 | 3.6e-125 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
FPANIOMK_00821 | 1.8e-262 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00822 | 6.8e-98 | S | GtrA-like protein | |||
FPANIOMK_00823 | 1.3e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
FPANIOMK_00824 | 1.3e-287 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
FPANIOMK_00825 | 0.0 | pepD | E | Peptidase family C69 | ||
FPANIOMK_00826 | 1.3e-107 | S | Phosphatidylethanolamine-binding protein | |||
FPANIOMK_00827 | 0.0 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
FPANIOMK_00828 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
FPANIOMK_00829 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
FPANIOMK_00830 | 5.9e-94 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
FPANIOMK_00831 | 2e-43 | S | Protein of unknown function (DUF1778) | |||
FPANIOMK_00832 | 3.3e-191 | 1.1.1.65 | C | Aldo/keto reductase family | ||
FPANIOMK_00834 | 4e-100 | M | Belongs to the glycosyl hydrolase 30 family | |||
FPANIOMK_00835 | 7.9e-17 | M | Belongs to the glycosyl hydrolase 30 family | |||
FPANIOMK_00837 | 1.4e-90 | pptA | 6.3.2.14 | Q | 4'-phosphopantetheinyl transferase superfamily | |
FPANIOMK_00838 | 5e-116 | K | WHG domain | |||
FPANIOMK_00839 | 4.8e-277 | 3.6.4.12 | K | Putative DNA-binding domain | ||
FPANIOMK_00840 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
FPANIOMK_00841 | 1.4e-281 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
FPANIOMK_00842 | 1e-107 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
FPANIOMK_00843 | 1.6e-143 | S | Putative ABC-transporter type IV | |||
FPANIOMK_00844 | 3.7e-254 | 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) | |
FPANIOMK_00845 | 6.2e-159 | L | Tetratricopeptide repeat | |||
FPANIOMK_00846 | 2.3e-190 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
FPANIOMK_00848 | 3.6e-137 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
FPANIOMK_00849 | 2e-102 | |||||
FPANIOMK_00850 | 6.8e-116 | trkA | P | TrkA-N domain | ||
FPANIOMK_00851 | 9.5e-235 | trkB | P | Cation transport protein | ||
FPANIOMK_00852 | 4.8e-182 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
FPANIOMK_00853 | 3.5e-292 | recN | L | May be involved in recombinational repair of damaged DNA | ||
FPANIOMK_00854 | 2e-123 | S | Haloacid dehalogenase-like hydrolase | |||
FPANIOMK_00855 | 3.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
FPANIOMK_00856 | 1.5e-175 | V | ATPases associated with a variety of cellular activities | |||
FPANIOMK_00857 | 1.8e-125 | S | ABC-2 family transporter protein | |||
FPANIOMK_00858 | 4.8e-123 | S | ABC-2 family transporter protein | |||
FPANIOMK_00859 | 1.9e-283 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
FPANIOMK_00860 | 4e-237 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
FPANIOMK_00861 | 1.6e-94 | |||||
FPANIOMK_00862 | 1.6e-145 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
FPANIOMK_00863 | 9.1e-192 | 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) | |
FPANIOMK_00865 | 2.1e-263 | 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 | |
FPANIOMK_00866 | 4.6e-68 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
FPANIOMK_00867 | 4.2e-138 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
FPANIOMK_00868 | 1.3e-78 | S | Bacterial PH domain | |||
FPANIOMK_00869 | 3.2e-255 | nplT | 3.2.1.1 | GH13 | G | Alpha amylase, catalytic domain |
FPANIOMK_00871 | 1.7e-104 | |||||
FPANIOMK_00872 | 5e-133 | C | Putative TM nitroreductase | |||
FPANIOMK_00873 | 8.1e-141 | yijF | S | Domain of unknown function (DUF1287) | ||
FPANIOMK_00874 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
FPANIOMK_00875 | 1.6e-146 | KT | RESPONSE REGULATOR receiver | |||
FPANIOMK_00876 | 2.4e-192 | V | VanZ like family | |||
FPANIOMK_00877 | 3.3e-109 | ycaK | 1.6.5.2 | S | NADPH-dependent FMN reductase | |
FPANIOMK_00878 | 1.9e-95 | ypjC | S | Putative ABC-transporter type IV | ||
FPANIOMK_00879 | 2.6e-158 | |||||
FPANIOMK_00881 | 6.4e-99 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00882 | 3e-28 | EGP | Major facilitator Superfamily | |||
FPANIOMK_00883 | 9.8e-164 | rpoC | M | heme binding | ||
FPANIOMK_00884 | 1.6e-79 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
FPANIOMK_00885 | 1e-80 | |||||
FPANIOMK_00886 | 1.4e-132 | S | SOS response associated peptidase (SRAP) | |||
FPANIOMK_00887 | 7.4e-22 | qseC | 2.7.13.3 | T | Histidine kinase | |
FPANIOMK_00888 | 6.6e-184 | S | Acetyltransferase (GNAT) domain | |||
FPANIOMK_00890 | 2e-30 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
FPANIOMK_00891 | 5.9e-101 | XK27_07525 | 3.6.1.55 | F | Hydrolase of X-linked nucleoside diphosphate N terminal | |
FPANIOMK_00892 | 4.3e-56 | K | Transcriptional regulator | |||
FPANIOMK_00893 | 1.2e-97 | MA20_25245 | K | FR47-like protein | ||
FPANIOMK_00894 | 1.2e-120 | ydaF_1 | J | Acetyltransferase (GNAT) domain | ||
FPANIOMK_00895 | 1.5e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
FPANIOMK_00896 | 1.3e-162 | 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 | |
FPANIOMK_00897 | 1.5e-283 | S | Psort location Cytoplasmic, score 8.87 | |||
FPANIOMK_00898 | 4.8e-108 | S | Domain of unknown function (DUF4194) | |||
FPANIOMK_00899 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
FPANIOMK_00900 | 4.7e-296 | E | Serine carboxypeptidase | |||
FPANIOMK_00901 | 2.6e-160 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
FPANIOMK_00902 | 3.7e-171 | corA | P | CorA-like Mg2+ transporter protein | ||
FPANIOMK_00903 | 5.8e-169 | ET | Bacterial periplasmic substrate-binding proteins | |||
FPANIOMK_00904 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FPANIOMK_00905 | 4.3e-91 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
FPANIOMK_00906 | 0.0 | comE | S | Competence protein | ||
FPANIOMK_00907 | 4.8e-182 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
FPANIOMK_00908 | 1.1e-118 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
FPANIOMK_00909 | 1e-159 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
FPANIOMK_00910 | 3.2e-101 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
FPANIOMK_00911 | 6.2e-196 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
FPANIOMK_00913 | 1.1e-133 | M | Peptidase family M23 | |||
FPANIOMK_00914 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
FPANIOMK_00915 | 3.2e-276 | G | ABC transporter substrate-binding protein | |||
FPANIOMK_00916 | 3.3e-241 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
FPANIOMK_00917 | 2.5e-200 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
FPANIOMK_00918 | 3.4e-91 | |||||
FPANIOMK_00919 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
FPANIOMK_00920 | 5.8e-88 | def | 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 | |
FPANIOMK_00921 | 1.4e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
FPANIOMK_00922 | 4.8e-146 | 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 | ||
FPANIOMK_00923 | 1.8e-127 | 3.2.1.8 | S | alpha beta | ||
FPANIOMK_00924 | 2.4e-133 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
FPANIOMK_00925 | 2.4e-93 | 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 | ||
FPANIOMK_00926 | 1.8e-176 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
FPANIOMK_00927 | 9.8e-230 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
FPANIOMK_00928 | 1.4e-139 | hisF | 4.1.3.27 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
FPANIOMK_00929 | 5.3e-74 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
FPANIOMK_00930 | 1.3e-309 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
FPANIOMK_00931 | 6.9e-245 | G | Bacterial extracellular solute-binding protein | |||
FPANIOMK_00932 | 1.1e-173 | G | Binding-protein-dependent transport system inner membrane component | |||
FPANIOMK_00933 | 1.7e-168 | G | ABC transporter permease | |||
FPANIOMK_00934 | 4.3e-62 | L | Transposase and inactivated derivatives IS30 family | |||
FPANIOMK_00935 | 1.3e-284 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
FPANIOMK_00936 | 6e-250 | V | ABC-2 family transporter protein | |||
FPANIOMK_00937 | 1.8e-226 | V | ABC-2 family transporter protein | |||
FPANIOMK_00938 | 6.9e-181 | V | ATPases associated with a variety of cellular activities | |||
FPANIOMK_00939 | 1.2e-42 | pacL | 3.6.3.8, 3.6.3.9 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
FPANIOMK_00940 | 9.2e-234 | T | Histidine kinase | |||
FPANIOMK_00941 | 3.1e-119 | K | helix_turn_helix, Lux Regulon | |||
FPANIOMK_00942 | 1.1e-115 | MA20_27875 | P | Protein of unknown function DUF47 | ||
FPANIOMK_00943 | 3.4e-189 | pit | P | Phosphate transporter family | ||
FPANIOMK_00944 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
FPANIOMK_00945 | 8.7e-303 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
FPANIOMK_00947 | 4.4e-51 | |||||
FPANIOMK_00948 | 1.2e-27 | |||||
FPANIOMK_00949 | 9.9e-112 | ysdA | S | Protein of unknown function (DUF1294) | ||
FPANIOMK_00951 | 1.7e-122 | |||||
FPANIOMK_00952 | 1e-281 | XK27_07020 | S | Domain of unknown function (DUF1846) | ||
FPANIOMK_00953 | 0.0 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
FPANIOMK_00954 | 9.8e-233 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
FPANIOMK_00955 | 1.7e-274 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
FPANIOMK_00956 | 2.9e-108 | 3.4.13.21 | E | Peptidase family S51 | ||
FPANIOMK_00957 | 4.2e-135 | L | Phage integrase family | |||
FPANIOMK_00959 | 2.6e-218 | ykiI | ||||
FPANIOMK_00960 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
FPANIOMK_00961 | 1.9e-127 | 3.6.1.13 | L | NUDIX domain | ||
FPANIOMK_00962 | 2.9e-173 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
FPANIOMK_00963 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
FPANIOMK_00964 | 9.2e-120 | pdtaR | T | Response regulator receiver domain protein | ||
FPANIOMK_00966 | 1.8e-110 | aspA | 3.6.1.13 | L | NUDIX domain | |
FPANIOMK_00967 | 1.9e-272 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
FPANIOMK_00968 | 5.6e-178 | terC | P | Integral membrane protein, TerC family | ||
FPANIOMK_00969 | 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 | ||
FPANIOMK_00970 | 2.7e-106 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
FPANIOMK_00971 | 3.3e-243 | rpsA | J | Ribosomal protein S1 | ||
FPANIOMK_00972 | 2.4e-164 | 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 | |
FPANIOMK_00973 | 5.6e-173 | P | Zinc-uptake complex component A periplasmic | |||
FPANIOMK_00974 | 2.8e-165 | znuC | P | ATPases associated with a variety of cellular activities | ||
FPANIOMK_00975 | 4.3e-139 | znuB | U | ABC 3 transport family | ||
FPANIOMK_00976 | 5.5e-83 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
FPANIOMK_00977 | 4.3e-101 | carD | K | CarD-like/TRCF domain | ||
FPANIOMK_00978 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
FPANIOMK_00979 | 1.9e-127 | T | Response regulator receiver domain protein | |||
FPANIOMK_00980 | 5e-204 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
FPANIOMK_00981 | 2.1e-72 | rulA | 3.4.21.88 | KT | Peptidase S24-like | |
FPANIOMK_00982 | 2e-129 | ctsW | S | Phosphoribosyl transferase domain | ||
FPANIOMK_00983 | 5e-156 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
FPANIOMK_00984 | 6.3e-66 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
FPANIOMK_00985 | 2.2e-266 | |||||
FPANIOMK_00986 | 0.0 | S | Glycosyl transferase, family 2 | |||
FPANIOMK_00987 | 5.8e-54 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
FPANIOMK_00988 | 2.4e-270 | K | Cell envelope-related transcriptional attenuator domain | |||
FPANIOMK_00989 | 0.0 | D | FtsK/SpoIIIE family | |||
FPANIOMK_00990 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
FPANIOMK_00991 | 4.7e-285 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
FPANIOMK_00992 | 2e-142 | yplQ | S | Haemolysin-III related | ||
FPANIOMK_00994 | 7.5e-80 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
FPANIOMK_00995 | 5.7e-73 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
FPANIOMK_00996 | 8.8e-281 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
FPANIOMK_00997 | 6.1e-97 | |||||
FPANIOMK_00999 | 2.6e-183 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
FPANIOMK_01000 | 2.8e-105 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
FPANIOMK_01001 | 2.5e-101 | divIC | D | Septum formation initiator | ||
FPANIOMK_01002 | 6.9e-245 | 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 | |
FPANIOMK_01003 | 6.4e-153 | pabC | 2.6.1.42, 2.6.1.85, 4.1.3.38 | E | branched-chain-amino-acid transaminase activity | |
FPANIOMK_01004 | 7.7e-296 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | chorismate binding enzyme | |
FPANIOMK_01005 | 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 | ||
FPANIOMK_01006 | 7.6e-114 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
FPANIOMK_01007 | 1.7e-96 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
FPANIOMK_01008 | 4.9e-145 | tagH | 3.6.3.38, 3.6.3.40 | GM | ABC transporter | |
FPANIOMK_01009 | 3.6e-151 | GM | ABC-2 type transporter | |||
FPANIOMK_01010 | 9.6e-197 | GM | GDP-mannose 4,6 dehydratase | |||
FPANIOMK_01011 | 5e-128 | ispD | 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
FPANIOMK_01013 | 3.1e-220 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
FPANIOMK_01014 | 0.0 | 2.7.8.14, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | ||
FPANIOMK_01015 | 1.4e-214 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
FPANIOMK_01016 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
FPANIOMK_01017 | 2.6e-228 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
FPANIOMK_01018 | 2.5e-95 | |||||
FPANIOMK_01019 | 2.2e-80 | |||||
FPANIOMK_01020 | 1.4e-142 | ytrE | V | ATPases associated with a variety of cellular activities | ||
FPANIOMK_01021 | 1.7e-191 | V | N-Acetylmuramoyl-L-alanine amidase | |||
FPANIOMK_01022 | 1.2e-258 | argE | E | Peptidase dimerisation domain | ||
FPANIOMK_01023 | 1.2e-103 | S | Protein of unknown function (DUF3043) | |||
FPANIOMK_01024 | 5.2e-281 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
FPANIOMK_01025 | 9.4e-144 | S | Domain of unknown function (DUF4191) | |||
FPANIOMK_01026 | 1.8e-286 | glnA | 6.3.1.2 | E | glutamine synthetase | |
FPANIOMK_01027 | 4.7e-10 | |||||
FPANIOMK_01029 | 1.6e-32 | traSA | D | DNA segregation ATPase FtsK SpoIIIE | ||
FPANIOMK_01033 | 5.2e-79 | S | GIY-YIG catalytic domain | |||
FPANIOMK_01034 | 7.8e-33 | 3.1.21.4 | L | Recognizes the double-stranded sequence CTCGAG and cleaves after C-1 | ||
FPANIOMK_01035 | 4.8e-115 | L | DNA restriction-modification system | |||
FPANIOMK_01036 | 2e-86 | int | L | Phage integrase, N-terminal SAM-like domain | ||
FPANIOMK_01037 | 8.2e-41 | |||||
FPANIOMK_01038 | 2.4e-74 | casA | L | CRISPR system CASCADE complex protein CasA | ||
FPANIOMK_01039 | 6.2e-75 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
FPANIOMK_01041 | 1.1e-302 | hsdM | 2.1.1.72 | V | modification (methylase) protein of type I restriction-modification system K03427 | |
FPANIOMK_01042 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
FPANIOMK_01044 | 3.8e-48 | S | Psort location Cytoplasmic, score 8.87 | |||
FPANIOMK_01045 | 1.8e-188 | 2.7.11.1 | KLT | Protein tyrosine kinase | ||
FPANIOMK_01046 | 9.6e-208 | 2.1.1.72 | H | Adenine-specific methyltransferase EcoRI | ||
FPANIOMK_01048 | 6.3e-26 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
FPANIOMK_01050 | 2.5e-194 | L | Phage integrase family | |||
FPANIOMK_01056 | 7.3e-247 | int | L | Phage integrase, N-terminal SAM-like domain | ||
FPANIOMK_01057 | 8.8e-161 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
FPANIOMK_01058 | 6.3e-210 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
FPANIOMK_01059 | 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 | |
FPANIOMK_01060 | 0.0 | S | Tetratricopeptide repeat | |||
FPANIOMK_01061 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
FPANIOMK_01062 | 2.3e-71 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
FPANIOMK_01063 | 4.9e-137 | bioM | P | ATPases associated with a variety of cellular activities | ||
FPANIOMK_01064 | 1.7e-212 | E | Aminotransferase class I and II | |||
FPANIOMK_01065 | 1.3e-139 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
FPANIOMK_01066 | 1.1e-104 | ribU | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | ||
FPANIOMK_01067 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
FPANIOMK_01068 | 1.2e-256 | EGP | Major facilitator Superfamily | |||
FPANIOMK_01070 | 2.2e-257 | rarA | L | Recombination factor protein RarA | ||
FPANIOMK_01071 | 0.0 | L | DEAD DEAH box helicase | |||
FPANIOMK_01072 | 6e-194 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
FPANIOMK_01073 | 4.8e-199 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_01074 | 1.8e-111 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_01075 | 4.3e-147 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
FPANIOMK_01076 | 3.6e-140 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
FPANIOMK_01077 | 6.5e-90 | S | Aminoacyl-tRNA editing domain | |||
FPANIOMK_01078 | 1e-73 | K | helix_turn_helix, Lux Regulon | |||
FPANIOMK_01079 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
FPANIOMK_01080 | 3.3e-250 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
FPANIOMK_01081 | 1.5e-216 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
FPANIOMK_01085 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
FPANIOMK_01086 | 4.7e-185 | uspA | T | Belongs to the universal stress protein A family | ||
FPANIOMK_01087 | 1.6e-202 | S | Protein of unknown function (DUF3027) | |||
FPANIOMK_01088 | 1e-66 | cspB | K | 'Cold-shock' DNA-binding domain | ||
FPANIOMK_01089 | 0.0 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
FPANIOMK_01090 | 1.6e-134 | KT | Response regulator receiver domain protein | |||
FPANIOMK_01091 | 4.9e-162 | |||||
FPANIOMK_01092 | 1.7e-10 | S | Proteins of 100 residues with WXG | |||
FPANIOMK_01093 | 2.7e-291 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
FPANIOMK_01094 | 2.2e-44 | cspA | K | 'Cold-shock' DNA-binding domain | ||
FPANIOMK_01095 | 3.4e-71 | S | LytR cell envelope-related transcriptional attenuator | |||
FPANIOMK_01096 | 2.3e-144 | 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 | |
FPANIOMK_01097 | 5e-196 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
FPANIOMK_01098 | 3.7e-174 | S | Protein of unknown function DUF58 | |||
FPANIOMK_01099 | 6.4e-94 | |||||
FPANIOMK_01100 | 1.5e-189 | S | von Willebrand factor (vWF) type A domain | |||
FPANIOMK_01101 | 1.6e-148 | S | von Willebrand factor (vWF) type A domain | |||
FPANIOMK_01102 | 2.7e-74 | |||||
FPANIOMK_01104 | 4.4e-291 | S | PGAP1-like protein | |||
FPANIOMK_01105 | 3e-281 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
FPANIOMK_01106 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
FPANIOMK_01107 | 8.1e-42 | hup | L | Belongs to the bacterial histone-like protein family | ||
FPANIOMK_01108 | 8.5e-276 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
FPANIOMK_01109 | 1.6e-10 | pup | S | Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation | ||
FPANIOMK_01110 | 3e-161 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
FPANIOMK_01111 | 0.0 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
FPANIOMK_01112 | 0.0 | arc | O | AAA ATPase forming ring-shaped complexes | ||
FPANIOMK_01113 | 1.1e-136 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
FPANIOMK_01114 | 5.6e-183 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
FPANIOMK_01115 | 3.2e-135 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
FPANIOMK_01116 | 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 | ||
FPANIOMK_01117 | 8.5e-221 | 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 | |
FPANIOMK_01118 | 1.1e-53 | 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 | |
FPANIOMK_01119 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
FPANIOMK_01120 | 5.5e-166 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
FPANIOMK_01122 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
FPANIOMK_01123 | 0.0 | ctpE | P | E1-E2 ATPase | ||
FPANIOMK_01124 | 8.3e-108 | |||||
FPANIOMK_01125 | 2.5e-247 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
FPANIOMK_01126 | 6.1e-124 | S | Protein of unknown function (DUF3159) | |||
FPANIOMK_01127 | 9.4e-139 | S | Protein of unknown function (DUF3710) | |||
FPANIOMK_01128 | 6.9e-169 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
FPANIOMK_01129 | 5.2e-262 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
FPANIOMK_01130 | 0.0 | oppA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
FPANIOMK_01131 | 0.0 | oppD | P | Belongs to the ABC transporter superfamily | ||
FPANIOMK_01132 | 1.3e-165 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
FPANIOMK_01133 | 7.9e-177 | appB | EP | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_01134 | 1.3e-187 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
FPANIOMK_01135 | 7.3e-42 | |||||
FPANIOMK_01136 | 1.9e-192 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
FPANIOMK_01137 | 5.5e-197 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
FPANIOMK_01138 | 3e-90 | |||||
FPANIOMK_01139 | 0.0 | typA | T | Elongation factor G C-terminus | ||
FPANIOMK_01140 | 5.7e-236 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
FPANIOMK_01141 | 1.4e-164 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, N-terminal domain | |
FPANIOMK_01142 | 0.0 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
FPANIOMK_01143 | 7.5e-252 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
FPANIOMK_01144 | 8.6e-150 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
FPANIOMK_01145 | 5.4e-113 | 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 | ||
FPANIOMK_01146 | 2.7e-149 | 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 | ||
FPANIOMK_01147 | 1.8e-152 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
FPANIOMK_01148 | 7.6e-180 | xerD | D | recombinase XerD | ||
FPANIOMK_01149 | 9.6e-62 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
FPANIOMK_01150 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
FPANIOMK_01151 | 6.2e-110 | 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 | ||
FPANIOMK_01153 | 1.9e-07 | S | Spermine/spermidine synthase domain | |||
FPANIOMK_01154 | 8e-134 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
FPANIOMK_01155 | 1e-198 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
FPANIOMK_01156 | 8.4e-93 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
FPANIOMK_01158 | 5.5e-178 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
FPANIOMK_01159 | 9.1e-194 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
FPANIOMK_01160 | 2e-64 | |||||
FPANIOMK_01161 | 8.1e-114 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
FPANIOMK_01162 | 4.8e-296 | 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 | |
FPANIOMK_01163 | 2.2e-190 | V | Acetyltransferase (GNAT) domain | |||
FPANIOMK_01164 | 2.4e-228 | 2.6.1.33 | M | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
FPANIOMK_01165 | 9.5e-244 | yxbA | 6.3.1.12 | S | ATP-grasp | |
FPANIOMK_01166 | 7.4e-129 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
FPANIOMK_01167 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
FPANIOMK_01168 | 1.4e-282 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
FPANIOMK_01170 | 4.3e-97 | 3.6.1.55 | F | NUDIX domain | ||
FPANIOMK_01171 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
FPANIOMK_01172 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
FPANIOMK_01173 | 5.1e-191 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_01174 | 6.7e-185 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_01175 | 7.4e-305 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
FPANIOMK_01176 | 1.6e-243 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
FPANIOMK_01177 | 6.6e-153 | 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 | |
FPANIOMK_01178 | 1.3e-215 | GK | ROK family | |||
FPANIOMK_01179 | 3.4e-132 | cutC | P | Participates in the control of copper homeostasis | ||
FPANIOMK_01180 | 6.2e-224 | GK | ROK family | |||
FPANIOMK_01181 | 1.9e-169 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
FPANIOMK_01182 | 1.3e-235 | G | Major Facilitator Superfamily | |||
FPANIOMK_01183 | 1.2e-85 | 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 | ||
FPANIOMK_01185 | 4.9e-37 | |||||
FPANIOMK_01186 | 3.6e-158 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
FPANIOMK_01187 | 3.4e-294 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
FPANIOMK_01188 | 6.5e-218 | 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) |
FPANIOMK_01189 | 4e-224 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
FPANIOMK_01190 | 2.7e-266 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
FPANIOMK_01191 | 3.6e-202 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
FPANIOMK_01192 | 2e-283 | 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 | |
FPANIOMK_01193 | 2.8e-180 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
FPANIOMK_01194 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
FPANIOMK_01195 | 9.7e-64 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
FPANIOMK_01196 | 7.8e-205 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
FPANIOMK_01197 | 1.3e-90 | mraZ | K | Belongs to the MraZ family | ||
FPANIOMK_01198 | 0.0 | L | DNA helicase | |||
FPANIOMK_01199 | 6.4e-229 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
FPANIOMK_01200 | 8.8e-83 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
FPANIOMK_01201 | 1.6e-45 | M | Lysin motif | |||
FPANIOMK_01202 | 7.5e-129 | 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 | |
FPANIOMK_01203 | 6e-166 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
FPANIOMK_01204 | 4.6e-177 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
FPANIOMK_01205 | 6.9e-273 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
FPANIOMK_01206 | 3.9e-173 | |||||
FPANIOMK_01207 | 3.1e-121 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
FPANIOMK_01208 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
FPANIOMK_01209 | 5e-177 | M | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses | |||
FPANIOMK_01210 | 2.1e-61 | EGP | Major facilitator Superfamily | |||
FPANIOMK_01211 | 4.7e-252 | S | Domain of unknown function (DUF5067) | |||
FPANIOMK_01212 | 2.1e-265 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
FPANIOMK_01213 | 4.9e-284 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
FPANIOMK_01214 | 4.9e-131 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
FPANIOMK_01215 | 1.4e-121 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
FPANIOMK_01216 | 1.7e-112 | |||||
FPANIOMK_01217 | 3.2e-112 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
FPANIOMK_01218 | 2.1e-224 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
FPANIOMK_01219 | 3.2e-256 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
FPANIOMK_01220 | 2.3e-181 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
FPANIOMK_01221 | 3e-07 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
FPANIOMK_01223 | 9.9e-76 | yneG | S | Domain of unknown function (DUF4186) | ||
FPANIOMK_01224 | 6.4e-173 | dkgA | 1.1.1.346 | C | Aldo/keto reductase family | |
FPANIOMK_01225 | 5e-156 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
FPANIOMK_01226 | 3.4e-202 | K | WYL domain | |||
FPANIOMK_01228 | 0.0 | 4.2.1.53 | S | MCRA family | ||
FPANIOMK_01229 | 2e-46 | yhbY | J | CRS1_YhbY | ||
FPANIOMK_01230 | 7.6e-106 | S | zinc-ribbon domain | |||
FPANIOMK_01231 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
FPANIOMK_01232 | 8.8e-39 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
FPANIOMK_01233 | 1.7e-15 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
FPANIOMK_01234 | 5.1e-192 | ywqG | S | Domain of unknown function (DUF1963) | ||
FPANIOMK_01235 | 1.5e-154 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
FPANIOMK_01236 | 1.3e-142 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
FPANIOMK_01237 | 1.2e-291 | I | acetylesterase activity | |||
FPANIOMK_01238 | 3.9e-235 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
FPANIOMK_01239 | 3.7e-221 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
FPANIOMK_01240 | 2.4e-183 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
FPANIOMK_01242 | 3.3e-23 | |||||
FPANIOMK_01243 | 5.7e-19 | |||||
FPANIOMK_01244 | 1.8e-144 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
FPANIOMK_01245 | 3e-76 | 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 | ||
FPANIOMK_01246 | 2.5e-163 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
FPANIOMK_01247 | 9.2e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
FPANIOMK_01248 | 5.9e-197 | ftsE | D | Cell division ATP-binding protein FtsE | ||
FPANIOMK_01249 | 3.7e-202 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
FPANIOMK_01250 | 7.5e-146 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
FPANIOMK_01251 | 6e-63 | |||||
FPANIOMK_01253 | 5.8e-177 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
FPANIOMK_01254 | 4e-103 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
FPANIOMK_01255 | 9.7e-90 | 3.1.21.3 | V | DivIVA protein | ||
FPANIOMK_01256 | 2.1e-42 | yggT | S | YGGT family | ||
FPANIOMK_01257 | 4.3e-80 | 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 | ||
FPANIOMK_01258 | 7.3e-231 | 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 | ||
FPANIOMK_01259 | 3.6e-246 | 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 | ||
FPANIOMK_01260 | 3e-300 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
FPANIOMK_01261 | 0.0 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
FPANIOMK_01262 | 6.1e-160 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
FPANIOMK_01263 | 0.0 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
FPANIOMK_01264 | 1.3e-84 | |||||
FPANIOMK_01265 | 6.9e-231 | O | AAA domain (Cdc48 subfamily) | |||
FPANIOMK_01266 | 4.1e-164 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
FPANIOMK_01267 | 1.2e-61 | S | Thiamine-binding protein | |||
FPANIOMK_01268 | 1.2e-196 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_01269 | 5.7e-47 | S | Protein of unknown function (DUF3052) | |||
FPANIOMK_01270 | 7.6e-152 | lon | T | Belongs to the peptidase S16 family | ||
FPANIOMK_01271 | 1.8e-284 | S | Zincin-like metallopeptidase | |||
FPANIOMK_01272 | 2.4e-281 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
FPANIOMK_01273 | 2.5e-227 | mphA | S | Aminoglycoside phosphotransferase | ||
FPANIOMK_01274 | 6.1e-32 | S | Protein of unknown function (DUF3107) | |||
FPANIOMK_01275 | 2.5e-166 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
FPANIOMK_01276 | 2e-115 | S | Vitamin K epoxide reductase | |||
FPANIOMK_01277 | 2.3e-170 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine | |
FPANIOMK_01278 | 1.5e-152 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
FPANIOMK_01279 | 1.2e-167 | S | Patatin-like phospholipase | |||
FPANIOMK_01280 | 0.0 | V | ABC transporter transmembrane region | |||
FPANIOMK_01281 | 0.0 | V | ABC transporter, ATP-binding protein | |||
FPANIOMK_01282 | 5.8e-89 | K | MarR family | |||
FPANIOMK_01284 | 6.4e-55 | plyA3 | M | Parallel beta-helix repeats | ||
FPANIOMK_01285 | 1.7e-24 | |||||
FPANIOMK_01286 | 2.7e-95 | |||||
FPANIOMK_01287 | 2.2e-117 | parA | D | AAA domain | ||
FPANIOMK_01288 | 1.5e-91 | S | Transcription factor WhiB | |||
FPANIOMK_01289 | 1.1e-42 | |||||
FPANIOMK_01290 | 3e-183 | S | Helix-turn-helix domain | |||
FPANIOMK_01291 | 7.8e-28 | |||||
FPANIOMK_01292 | 1.7e-118 | |||||
FPANIOMK_01293 | 4.3e-132 | |||||
FPANIOMK_01294 | 8.4e-71 | |||||
FPANIOMK_01295 | 9.8e-128 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
FPANIOMK_01296 | 5.5e-166 | S | Sucrose-6F-phosphate phosphohydrolase | |||
FPANIOMK_01297 | 2.1e-94 | P | ABC-type metal ion transport system permease component | |||
FPANIOMK_01298 | 2.7e-224 | S | Peptidase dimerisation domain | |||
FPANIOMK_01299 | 0.0 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
FPANIOMK_01300 | 4.9e-40 | |||||
FPANIOMK_01301 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
FPANIOMK_01302 | 3.9e-175 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
FPANIOMK_01303 | 1.3e-113 | S | Protein of unknown function (DUF3000) | |||
FPANIOMK_01304 | 2.4e-250 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
FPANIOMK_01305 | 2.8e-236 | 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 | ||
FPANIOMK_01306 | 3.6e-255 | clcA_2 | P | Voltage gated chloride channel | ||
FPANIOMK_01307 | 1.1e-112 | 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 | |
FPANIOMK_01308 | 1.5e-127 | 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 | |
FPANIOMK_01309 | 5.9e-244 | 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 | ||
FPANIOMK_01312 | 1e-234 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
FPANIOMK_01313 | 1.2e-225 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
FPANIOMK_01314 | 8.4e-168 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
FPANIOMK_01315 | 4.4e-118 | safC | S | O-methyltransferase | ||
FPANIOMK_01316 | 6.6e-184 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
FPANIOMK_01317 | 3e-71 | yraN | L | Belongs to the UPF0102 family | ||
FPANIOMK_01318 | 7.2e-294 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
FPANIOMK_01319 | 5.1e-284 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
FPANIOMK_01320 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
FPANIOMK_01321 | 1.5e-166 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
FPANIOMK_01322 | 1.6e-157 | S | Putative ABC-transporter type IV | |||
FPANIOMK_01323 | 2.6e-252 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
FPANIOMK_01324 | 3.4e-162 | V | ABC transporter, ATP-binding protein | |||
FPANIOMK_01325 | 0.0 | MV | MacB-like periplasmic core domain | |||
FPANIOMK_01326 | 0.0 | phoN | I | PAP2 superfamily | ||
FPANIOMK_01327 | 6.1e-132 | K | helix_turn_helix, Lux Regulon | |||
FPANIOMK_01328 | 0.0 | tcsS2 | T | Histidine kinase | ||
FPANIOMK_01329 | 1.9e-264 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
FPANIOMK_01330 | 4e-142 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
FPANIOMK_01331 | 1.9e-167 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
FPANIOMK_01332 | 3.2e-147 | P | NLPA lipoprotein | |||
FPANIOMK_01333 | 5.9e-188 | acoA | 1.2.4.1 | C | Dehydrogenase E1 component | |
FPANIOMK_01334 | 3.9e-182 | 1.2.4.1 | C | Pyruvate 2-oxoglutarate dehydrogenase complex dehydrogenase (E1) component eukaryotic type beta subunit | ||
FPANIOMK_01335 | 1.6e-205 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
FPANIOMK_01336 | 2.9e-93 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
FPANIOMK_01337 | 5.4e-228 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
FPANIOMK_01338 | 1.2e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
FPANIOMK_01339 | 3.1e-194 | int | L | Phage integrase, N-terminal SAM-like domain | ||
FPANIOMK_01340 | 1.7e-27 | S | Protein of unknown function (DUF3800) | |||
FPANIOMK_01341 | 9.7e-30 | |||||
FPANIOMK_01342 | 6.8e-08 | int | L | Phage integrase, N-terminal SAM-like domain | ||
FPANIOMK_01343 | 2.6e-119 | dprA | LU | DNA recombination-mediator protein A | ||
FPANIOMK_01344 | 8.2e-61 | S | competence protein | |||
FPANIOMK_01345 | 3.4e-09 | |||||
FPANIOMK_01348 | 4.6e-16 | |||||
FPANIOMK_01349 | 5.4e-64 | L | Integrase core domain | |||
FPANIOMK_01350 | 0.0 | hsdM | 2.1.1.72 | V | modification (methylase) protein of type I restriction-modification system K03427 | |
FPANIOMK_01351 | 1e-156 | S | Domain of unknown function (DUF4357) | |||
FPANIOMK_01352 | 2.4e-30 | |||||
FPANIOMK_01353 | 5.6e-37 | hsdS | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
FPANIOMK_01354 | 3.1e-158 | L | Phage integrase family | |||
FPANIOMK_01355 | 1.7e-53 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
FPANIOMK_01356 | 4.1e-239 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
FPANIOMK_01357 | 1.1e-84 | argR | K | Regulates arginine biosynthesis genes | ||
FPANIOMK_01358 | 5e-184 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
FPANIOMK_01359 | 2.5e-247 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
FPANIOMK_01360 | 1.7e-179 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
FPANIOMK_01361 | 5.7e-214 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
FPANIOMK_01362 | 1e-204 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
FPANIOMK_01363 | 1.4e-89 | |||||
FPANIOMK_01364 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
FPANIOMK_01365 | 7e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
FPANIOMK_01366 | 2.4e-161 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
FPANIOMK_01367 | 7.6e-135 | ybbL | V | ATPases associated with a variety of cellular activities | ||
FPANIOMK_01368 | 2.5e-136 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
FPANIOMK_01369 | 3e-53 | IQ | oxidoreductase activity | |||
FPANIOMK_01371 | 1.1e-90 | K | AraC-like ligand binding domain | |||
FPANIOMK_01372 | 1.4e-237 | rutG | F | Permease family | ||
FPANIOMK_01373 | 4e-158 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
FPANIOMK_01374 | 2.4e-63 | S | Phospholipase/Carboxylesterase | |||
FPANIOMK_01375 | 8.3e-188 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
FPANIOMK_01376 | 2.5e-144 | rlrG | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
FPANIOMK_01377 | 9.2e-118 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
FPANIOMK_01378 | 1.6e-288 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
FPANIOMK_01380 | 0.0 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
FPANIOMK_01381 | 7.2e-126 | ypfH | S | Phospholipase/Carboxylesterase | ||
FPANIOMK_01382 | 2.7e-73 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
FPANIOMK_01383 | 2.5e-24 | |||||
FPANIOMK_01384 | 2.1e-34 | yhcC | S | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | ||
FPANIOMK_01385 | 2.8e-66 | S | Zincin-like metallopeptidase | |||
FPANIOMK_01386 | 2.7e-87 | S | Helix-turn-helix | |||
FPANIOMK_01387 | 1.3e-197 | S | Short C-terminal domain | |||
FPANIOMK_01388 | 2.7e-22 | |||||
FPANIOMK_01389 | 1.2e-148 | |||||
FPANIOMK_01390 | 1e-78 | K | Psort location Cytoplasmic, score | |||
FPANIOMK_01391 | 1.3e-256 | KLT | Protein tyrosine kinase | |||
FPANIOMK_01392 | 7.9e-66 | S | Cupin 2, conserved barrel domain protein | |||
FPANIOMK_01393 | 2.1e-157 | ksgA | 2.1.1.182 | J | Methyltransferase domain | |
FPANIOMK_01394 | 5.6e-59 | yccF | S | Inner membrane component domain | ||
FPANIOMK_01395 | 8.6e-120 | E | Psort location Cytoplasmic, score 8.87 | |||
FPANIOMK_01396 | 4.3e-27 | L | DNA integration | |||
FPANIOMK_01397 | 1.1e-26 | |||||
FPANIOMK_01398 | 1.2e-140 | fic | D | Fic/DOC family | ||
FPANIOMK_01399 | 4.3e-234 | L | Phage integrase family | |||
FPANIOMK_01400 | 9.4e-28 | |||||
FPANIOMK_01401 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
FPANIOMK_01402 | 2.2e-84 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
FPANIOMK_01403 | 1.4e-47 | S | Domain of unknown function (DUF4193) | |||
FPANIOMK_01404 | 1.4e-187 | S | Protein of unknown function (DUF3071) | |||
FPANIOMK_01405 | 1.3e-237 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
FPANIOMK_01406 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
FPANIOMK_01407 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
FPANIOMK_01408 | 1.2e-36 | K | Transcriptional regulator | |||
FPANIOMK_01409 | 7.6e-277 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
FPANIOMK_01410 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
FPANIOMK_01411 | 2e-179 | 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 | ||
FPANIOMK_01412 | 5e-122 | |||||
FPANIOMK_01413 | 3e-201 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
FPANIOMK_01414 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
FPANIOMK_01415 | 5.1e-133 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
FPANIOMK_01416 | 1.5e-109 | |||||
FPANIOMK_01417 | 7.9e-191 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
FPANIOMK_01418 | 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 | ||
FPANIOMK_01419 | 1.3e-109 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
FPANIOMK_01421 | 6.1e-27 | marR5 | K | Winged helix DNA-binding domain | ||
FPANIOMK_01422 | 1.6e-73 | recX | S | Modulates RecA activity | ||
FPANIOMK_01423 | 8e-216 | 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 | ||
FPANIOMK_01424 | 3.7e-40 | S | Protein of unknown function (DUF3046) | |||
FPANIOMK_01425 | 7.3e-81 | K | Helix-turn-helix XRE-family like proteins | |||
FPANIOMK_01426 | 1.3e-96 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
FPANIOMK_01427 | 2e-123 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
FPANIOMK_01428 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
FPANIOMK_01429 | 2e-137 | fic | D | Fic/DOC family | ||
FPANIOMK_01430 | 9e-185 | 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) | |
FPANIOMK_01431 | 1.3e-279 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
FPANIOMK_01432 | 3.2e-121 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
FPANIOMK_01433 | 3e-168 | ydeD | EG | EamA-like transporter family | ||
FPANIOMK_01434 | 6.6e-132 | ybhL | S | Belongs to the BI1 family | ||
FPANIOMK_01435 | 2.8e-95 | S | Domain of unknown function (DUF5067) | |||
FPANIOMK_01436 | 1.7e-265 | T | Histidine kinase | |||
FPANIOMK_01437 | 1.1e-116 | K | helix_turn_helix, Lux Regulon | |||
FPANIOMK_01438 | 0.0 | S | Protein of unknown function DUF262 | |||
FPANIOMK_01439 | 2e-302 | gmk | 2.4.2.10, 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
FPANIOMK_01440 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
FPANIOMK_01441 | 6.9e-239 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
FPANIOMK_01442 | 1.2e-94 | 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 | ||
FPANIOMK_01443 | 3.3e-103 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
FPANIOMK_01445 | 3.8e-211 | EGP | Transmembrane secretion effector | |||
FPANIOMK_01446 | 6e-146 | S | Esterase-like activity of phytase | |||
FPANIOMK_01447 | 1.3e-174 | S | Esterase-like activity of phytase | |||
FPANIOMK_01448 | 8.1e-232 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
FPANIOMK_01449 | 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 | ||
FPANIOMK_01450 | 3.3e-80 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
FPANIOMK_01451 | 9.3e-62 | 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 | ||
FPANIOMK_01453 | 2.5e-197 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
FPANIOMK_01454 | 5.4e-228 | M | Glycosyl transferase 4-like domain | |||
FPANIOMK_01455 | 0.0 | M | Parallel beta-helix repeats | |||
FPANIOMK_01456 | 1.4e-234 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
FPANIOMK_01457 | 3.8e-139 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
FPANIOMK_01458 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
FPANIOMK_01459 | 3e-114 | |||||
FPANIOMK_01460 | 6.4e-95 | S | Protein of unknown function (DUF4230) | |||
FPANIOMK_01461 | 2e-149 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
FPANIOMK_01462 | 7.1e-28 | K | DNA-binding transcription factor activity | |||
FPANIOMK_01463 | 1.8e-68 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
FPANIOMK_01464 | 2e-32 | |||||
FPANIOMK_01465 | 4.4e-302 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
FPANIOMK_01466 | 1.3e-292 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
FPANIOMK_01467 | 2e-186 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
FPANIOMK_01468 | 5e-240 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
FPANIOMK_01469 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
FPANIOMK_01470 | 2.7e-247 | S | Putative esterase | |||
FPANIOMK_01471 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
FPANIOMK_01472 | 1e-162 | P | Zinc-uptake complex component A periplasmic | |||
FPANIOMK_01473 | 2.7e-140 | S | cobalamin synthesis protein | |||
FPANIOMK_01474 | 2.3e-47 | rpmB | J | Ribosomal L28 family | ||
FPANIOMK_01475 | 7.5e-49 | 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 | ||
FPANIOMK_01476 | 2e-42 | rpmE2 | J | Ribosomal protein L31 | ||
FPANIOMK_01477 | 3.1e-14 | rpmJ | J | Ribosomal protein L36 | ||
FPANIOMK_01478 | 2.3e-23 | J | Ribosomal L32p protein family | |||
FPANIOMK_01479 | 3.1e-201 | ycgR | S | Predicted permease | ||
FPANIOMK_01480 | 2.6e-154 | S | TIGRFAM TIGR03943 family protein | |||
FPANIOMK_01481 | 2.6e-45 | |||||
FPANIOMK_01482 | 5.6e-73 | zur | P | Belongs to the Fur family | ||
FPANIOMK_01483 | 6.2e-229 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
FPANIOMK_01484 | 4.7e-85 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
FPANIOMK_01485 | 8.5e-179 | adh3 | C | Zinc-binding dehydrogenase | ||
FPANIOMK_01486 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
FPANIOMK_01488 | 7.5e-175 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
FPANIOMK_01489 | 2.9e-42 | S | Memo-like protein | |||
FPANIOMK_01490 | 1.2e-227 | K | Putative ATP-dependent DNA helicase recG C-terminal | |||
FPANIOMK_01491 | 2.5e-158 | K | Helix-turn-helix domain, rpiR family | |||
FPANIOMK_01492 | 1.8e-167 | L | Transposase and inactivated derivatives IS30 family | |||
FPANIOMK_01493 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
FPANIOMK_01494 | 2.3e-248 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
FPANIOMK_01495 | 2e-263 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
FPANIOMK_01496 | 1.5e-269 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
FPANIOMK_01497 | 7.1e-94 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
FPANIOMK_01498 | 1.4e-10 | 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) | |
FPANIOMK_01499 | 2.3e-92 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
FPANIOMK_01500 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
FPANIOMK_01501 | 2.4e-220 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
FPANIOMK_01502 | 4e-192 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
FPANIOMK_01503 | 4.4e-109 | |||||
FPANIOMK_01504 | 0.0 | XK27_00515 | D | Cell surface antigen C-terminus | ||
FPANIOMK_01505 | 8.9e-26 | |||||
FPANIOMK_01506 | 3e-140 | |||||
FPANIOMK_01507 | 1e-62 | S | PrgI family protein | |||
FPANIOMK_01508 | 0.0 | trsE | U | type IV secretory pathway VirB4 | ||
FPANIOMK_01509 | 2.2e-206 | isp2 | 3.2.1.96 | M | CHAP domain | |
FPANIOMK_01510 | 3.6e-14 | U | Type IV secretory system Conjugative DNA transfer | |||
FPANIOMK_01511 | 4.3e-118 | |||||
FPANIOMK_01512 | 5.9e-101 | K | DNA binding | |||
FPANIOMK_01513 | 2.4e-101 | dam2 | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
FPANIOMK_01514 | 8.8e-09 | |||||
FPANIOMK_01515 | 0.0 | U | Type IV secretory system Conjugative DNA transfer | |||
FPANIOMK_01516 | 9.3e-31 | |||||
FPANIOMK_01517 | 7.1e-39 | |||||
FPANIOMK_01518 | 0.0 | XK27_00500 | KL | Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair | ||
FPANIOMK_01520 | 5e-284 | |||||
FPANIOMK_01521 | 1.1e-163 | S | Protein of unknown function (DUF3801) | |||
FPANIOMK_01522 | 5.4e-279 | ltrBE1 | U | Relaxase/Mobilisation nuclease domain | ||
FPANIOMK_01523 | 6.9e-52 | S | Bacterial mobilisation protein (MobC) | |||
FPANIOMK_01524 | 1.8e-40 | S | Protein of unknown function (DUF2442) | |||
FPANIOMK_01525 | 3e-55 | |||||
FPANIOMK_01526 | 1.5e-86 | |||||
FPANIOMK_01527 | 0.0 | topB | 5.99.1.2 | L | DNA topoisomerase | |
FPANIOMK_01528 | 1.3e-82 | |||||
FPANIOMK_01529 | 9.4e-60 | |||||
FPANIOMK_01530 | 1.3e-47 | |||||
FPANIOMK_01531 | 1.2e-211 | S | HipA-like C-terminal domain | |||
FPANIOMK_01532 | 0.0 | rgpF | M | Rhamnan synthesis protein F | ||
FPANIOMK_01533 | 2.5e-294 | S | Tetratricopeptide repeat | |||
FPANIOMK_01534 | 1.3e-208 | rgpD | 3.6.3.38 | GM | ABC transporter, ATP-binding protein | |
FPANIOMK_01535 | 8.7e-131 | rgpC | U | Transport permease protein | ||
FPANIOMK_01536 | 1.2e-168 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
FPANIOMK_01537 | 1e-153 | L | Transposase, Mutator family | |||
FPANIOMK_01538 | 4.5e-80 | L | PFAM Integrase catalytic | |||
FPANIOMK_01539 | 9.1e-111 | L | HTH-like domain | |||
FPANIOMK_01540 | 1.7e-16 | L | Transposase | |||
FPANIOMK_01541 | 4.4e-45 | L | Transposase DDE domain | |||
FPANIOMK_01542 | 1.6e-290 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
FPANIOMK_01543 | 1.6e-260 | 3.6.4.12 | K | Putative DNA-binding domain | ||
FPANIOMK_01544 | 8.2e-201 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
FPANIOMK_01545 | 0.0 | |||||
FPANIOMK_01546 | 1.4e-173 | rfbJ | M | Glycosyl transferase family 2 | ||
FPANIOMK_01547 | 0.0 | lytC | 2.1.1.197, 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
FPANIOMK_01548 | 1.8e-28 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
FPANIOMK_01549 | 2.3e-203 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
FPANIOMK_01550 | 7.3e-89 | T | protein histidine kinase activity | |||
FPANIOMK_01551 | 3.8e-88 | K | LytTr DNA-binding domain | |||
FPANIOMK_01552 | 1e-47 | S | Protein of unknown function (DUF3073) | |||
FPANIOMK_01553 | 6.5e-204 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FPANIOMK_01554 | 1.8e-195 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
FPANIOMK_01555 | 5.2e-17 | S | Amidohydrolase family | |||
FPANIOMK_01556 | 1.1e-155 | S | Amidohydrolase family | |||
FPANIOMK_01557 | 0.0 | yjjP | S | Threonine/Serine exporter, ThrE | ||
FPANIOMK_01558 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
FPANIOMK_01559 | 4.3e-239 | yhjX | EGP | Major facilitator Superfamily | ||
FPANIOMK_01560 | 6.5e-309 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
FPANIOMK_01561 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
FPANIOMK_01562 | 2.9e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
FPANIOMK_01563 | 6.9e-119 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
FPANIOMK_01564 | 1.9e-95 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_01565 | 1.2e-241 | ytfL | P | Transporter associated domain | ||
FPANIOMK_01566 | 1.3e-188 | yddG | EG | EamA-like transporter family | ||
FPANIOMK_01567 | 1.9e-83 | dps | P | Belongs to the Dps family | ||
FPANIOMK_01568 | 2.3e-136 | S | Protein of unknown function DUF45 | |||
FPANIOMK_01569 | 5.2e-252 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
FPANIOMK_01570 | 3.3e-40 | ulaC | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
FPANIOMK_01571 | 3.3e-77 | ulaC | 2.7.1.194, 2.7.1.197, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
FPANIOMK_01572 | 1.4e-187 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_01573 | 0.0 | G | Glycosyl hydrolase family 20, domain 2 | |||
FPANIOMK_01576 | 0.0 | 3.2.1.55 | GH51 | G | arabinose metabolic process | |
FPANIOMK_01577 | 2.5e-50 | 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 | ||
FPANIOMK_01578 | 5.6e-124 | gntR | K | FCD | ||
FPANIOMK_01579 | 2.3e-259 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
FPANIOMK_01581 | 8.3e-09 | K | helix_turn _helix lactose operon repressor | |||
FPANIOMK_01582 | 1.2e-227 | I | Serine aminopeptidase, S33 | |||
FPANIOMK_01583 | 7.9e-187 | K | Periplasmic binding protein domain | |||
FPANIOMK_01584 | 3.5e-187 | G | Glycosyl hydrolases family 43 | |||
FPANIOMK_01585 | 1.2e-06 | S | Parallel beta-helix repeats | |||
FPANIOMK_01586 | 6.7e-72 | S | Transmembrane domain of unknown function (DUF3566) | |||
FPANIOMK_01587 | 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 | |
FPANIOMK_01588 | 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 | |
FPANIOMK_01589 | 3.2e-93 | S | Protein of unknown function (DUF721) | |||
FPANIOMK_01590 | 4.7e-241 | 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 | ||
FPANIOMK_01591 | 6e-205 | 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 | |
FPANIOMK_01592 | 7.8e-299 | 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 | ||
FPANIOMK_01593 | 4.5e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
FPANIOMK_01594 | 1e-171 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
FPANIOMK_01595 | 8.6e-93 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
FPANIOMK_01596 | 6.5e-125 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
FPANIOMK_01597 | 8.5e-179 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
FPANIOMK_01598 | 1.2e-242 | parB | K | Belongs to the ParB family | ||
FPANIOMK_01599 | 4.7e-202 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
FPANIOMK_01600 | 0.0 | murJ | KLT | MviN-like protein | ||
FPANIOMK_01601 | 0.0 | M | Conserved repeat domain | |||
FPANIOMK_01602 | 5.2e-124 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
FPANIOMK_01603 | 1e-278 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
FPANIOMK_01604 | 1.5e-112 | S | LytR cell envelope-related transcriptional attenuator | |||
FPANIOMK_01605 | 4.2e-168 | 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 | |
FPANIOMK_01606 | 6.3e-171 | ksgA | 2.1.1.182, 2.1.1.184 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
FPANIOMK_01607 | 7.6e-211 | S | G5 | |||
FPANIOMK_01609 | 4.2e-150 | O | Thioredoxin | |||
FPANIOMK_01610 | 0.0 | KLT | Protein tyrosine kinase | |||
FPANIOMK_01611 | 1.3e-173 | K | Psort location Cytoplasmic, score | |||
FPANIOMK_01612 | 4.3e-211 | ugpC | E | Belongs to the ABC transporter superfamily | ||
FPANIOMK_01613 | 9.5e-103 | L | Helix-turn-helix domain | |||
FPANIOMK_01614 | 0.0 | S | LPXTG-motif cell wall anchor domain protein | |||
FPANIOMK_01615 | 4.9e-253 | M | LPXTG-motif cell wall anchor domain protein | |||
FPANIOMK_01616 | 7.7e-180 | 3.4.22.70 | M | Sortase family | ||
FPANIOMK_01617 | 1.7e-154 | |||||
FPANIOMK_01618 | 1e-270 | KLT | Domain of unknown function (DUF4032) | |||
FPANIOMK_01619 | 9.9e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
FPANIOMK_01621 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
FPANIOMK_01622 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
FPANIOMK_01623 | 5.3e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
FPANIOMK_01624 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
FPANIOMK_01625 | 1.2e-145 | ypfH | S | Phospholipase/Carboxylesterase | ||
FPANIOMK_01626 | 1.1e-83 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
FPANIOMK_01627 | 1.3e-234 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
FPANIOMK_01628 | 3e-144 | cobB2 | K | Sir2 family | ||
FPANIOMK_01629 | 5.3e-44 | A | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | |||
FPANIOMK_01632 | 6.5e-42 | S | Protein of unknwon function (DUF3310) | |||
FPANIOMK_01634 | 3.2e-35 | A | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | |||
FPANIOMK_01635 | 7.6e-09 | |||||
FPANIOMK_01638 | 4.5e-10 | |||||
FPANIOMK_01640 | 3.9e-91 | J | tRNA 5'-leader removal | |||
FPANIOMK_01642 | 3.7e-44 | V | HNH nucleases | |||
FPANIOMK_01643 | 9.7e-18 | |||||
FPANIOMK_01644 | 4.1e-177 | S | Terminase | |||
FPANIOMK_01645 | 2.6e-211 | S | Phage portal protein, SPP1 Gp6-like | |||
FPANIOMK_01646 | 8.8e-90 | |||||
FPANIOMK_01648 | 6e-54 | |||||
FPANIOMK_01649 | 3.1e-135 | V | Phage capsid family | |||
FPANIOMK_01651 | 8.7e-48 | S | Phage protein Gp19/Gp15/Gp42 | |||
FPANIOMK_01652 | 8.7e-24 | |||||
FPANIOMK_01653 | 1e-24 | |||||
FPANIOMK_01654 | 6.4e-48 | |||||
FPANIOMK_01655 | 1.1e-113 | N | domain, Protein | |||
FPANIOMK_01656 | 6e-35 | |||||
FPANIOMK_01657 | 4.5e-105 | S | phage tail tape measure protein | |||
FPANIOMK_01658 | 3.7e-58 | |||||
FPANIOMK_01659 | 1.8e-82 | S | Psort location Cytoplasmic, score | |||
FPANIOMK_01662 | 2.6e-95 | |||||
FPANIOMK_01664 | 5.9e-37 | |||||
FPANIOMK_01666 | 7.8e-45 | |||||
FPANIOMK_01667 | 1.4e-89 | L | DNA integration | |||
FPANIOMK_01669 | 2.9e-45 | S | SPP1 phage holin | |||
FPANIOMK_01670 | 1.5e-132 | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
FPANIOMK_01672 | 1e-160 | L | Phage integrase family | |||
FPANIOMK_01673 | 9e-62 | |||||
FPANIOMK_01674 | 2e-53 | |||||
FPANIOMK_01677 | 2.4e-26 | |||||
FPANIOMK_01679 | 1.1e-07 | |||||
FPANIOMK_01682 | 1.2e-52 | ssb1 | L | Single-stranded DNA-binding protein | ||
FPANIOMK_01683 | 5.1e-13 | |||||
FPANIOMK_01685 | 5.3e-81 | K | ParB-like nuclease domain | |||
FPANIOMK_01687 | 1.2e-85 | |||||
FPANIOMK_01688 | 1.2e-64 | D | MobA/MobL family | |||
FPANIOMK_01689 | 2.8e-46 | L | Transposase | |||
FPANIOMK_01690 | 3.4e-89 | tnp7109-21 | L | Integrase core domain | ||
FPANIOMK_01691 | 1.1e-26 | 2.1.1.72 | S | Adenine-specific methyltransferase EcoRI | ||
FPANIOMK_01692 | 2.4e-40 | |||||
FPANIOMK_01693 | 5.6e-112 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
FPANIOMK_01695 | 1.4e-46 | 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 | |
FPANIOMK_01697 | 2.8e-241 | pbuX | F | Permease family | ||
FPANIOMK_01698 | 3e-107 | 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 | |
FPANIOMK_01699 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
FPANIOMK_01700 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
FPANIOMK_01701 | 8.2e-64 | S | Domain of unknown function (DUF4418) | |||
FPANIOMK_01702 | 1.9e-212 | V | FtsX-like permease family | |||
FPANIOMK_01703 | 1.3e-127 | lolD | V | ABC transporter | ||
FPANIOMK_01704 | 1e-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 | ||
FPANIOMK_01705 | 0.0 | oatA | I | Psort location CytoplasmicMembrane, score 9.99 | ||
FPANIOMK_01706 | 3.3e-135 | pgm3 | G | Phosphoglycerate mutase family | ||
FPANIOMK_01707 | 3.8e-64 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
FPANIOMK_01708 | 1.1e-36 | |||||
FPANIOMK_01709 | 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 | |
FPANIOMK_01710 | 3e-75 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
FPANIOMK_01711 | 7.1e-188 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
FPANIOMK_01712 | 1.3e-47 | 3.4.23.43 | S | Type IV leader peptidase family | ||
FPANIOMK_01713 | 6e-219 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
FPANIOMK_01714 | 0.0 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
FPANIOMK_01715 | 2.2e-78 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
FPANIOMK_01716 | 3.4e-15 | |||||
FPANIOMK_01717 | 1.7e-120 | K | helix_turn_helix, Lux Regulon | |||
FPANIOMK_01718 | 2.6e-07 | 3.4.22.70 | M | Sortase family | ||
FPANIOMK_01719 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
FPANIOMK_01720 | 3.6e-290 | sufB | O | FeS assembly protein SufB | ||
FPANIOMK_01721 | 1.4e-234 | sufD | O | FeS assembly protein SufD | ||
FPANIOMK_01722 | 1.4e-144 | sufC | O | FeS assembly ATPase SufC | ||
FPANIOMK_01723 | 3.5e-241 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
FPANIOMK_01724 | 8.8e-101 | iscU | C | SUF system FeS assembly protein, NifU family | ||
FPANIOMK_01725 | 1.2e-108 | yitW | S | Iron-sulfur cluster assembly protein | ||
FPANIOMK_01726 | 4.7e-243 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
FPANIOMK_01727 | 4e-164 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
FPANIOMK_01729 | 1.4e-134 | 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 | |
FPANIOMK_01730 | 4.4e-58 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
FPANIOMK_01731 | 2e-197 | phoH | T | PhoH-like protein | ||
FPANIOMK_01732 | 7.4e-100 | 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 | |
FPANIOMK_01733 | 2.4e-251 | corC | S | CBS domain | ||
FPANIOMK_01734 | 5.1e-187 | 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 | ||
FPANIOMK_01735 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
FPANIOMK_01736 | 3.1e-201 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
FPANIOMK_01737 | 4.4e-44 | pntA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
FPANIOMK_01738 | 2.3e-233 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
FPANIOMK_01739 | 4.8e-190 | S | alpha beta | |||
FPANIOMK_01740 | 7.7e-93 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
FPANIOMK_01741 | 2.4e-225 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
FPANIOMK_01742 | 1.8e-46 | S | phosphoesterase or phosphohydrolase | |||
FPANIOMK_01743 | 6e-99 | 3.1.4.37 | T | RNA ligase | ||
FPANIOMK_01744 | 1.2e-135 | S | UPF0126 domain | |||
FPANIOMK_01745 | 9.9e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
FPANIOMK_01746 | 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 | ||
FPANIOMK_01747 | 2e-242 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
FPANIOMK_01748 | 4e-13 | S | Membrane | |||
FPANIOMK_01749 | 1.1e-292 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
FPANIOMK_01750 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
FPANIOMK_01751 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
FPANIOMK_01752 | 1e-303 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
FPANIOMK_01753 | 3.6e-82 | |||||
FPANIOMK_01754 | 8.7e-245 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
FPANIOMK_01755 | 5.7e-163 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
FPANIOMK_01756 | 1.5e-150 | ybeM | S | Carbon-nitrogen hydrolase | ||
FPANIOMK_01757 | 3e-50 | S | Sel1-like repeats. | |||
FPANIOMK_01758 | 1.2e-185 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
FPANIOMK_01759 | 1.7e-61 | S | Short C-terminal domain | |||
FPANIOMK_01760 | 1.1e-139 | L | Transposase | |||
FPANIOMK_01761 | 1.6e-28 | |||||
FPANIOMK_01762 | 2.3e-31 | XK26_04895 | ||||
FPANIOMK_01763 | 5.1e-22 | XK26_04895 | ||||
FPANIOMK_01764 | 0.0 | KL | Type III restriction enzyme res subunit | |||
FPANIOMK_01765 | 9.5e-38 | L | Eco57I restriction-modification methylase | |||
FPANIOMK_01766 | 5.3e-56 | L | Eco57I restriction-modification methylase | |||
FPANIOMK_01767 | 2.8e-182 | 3.1.21.4 | V | Type III restriction enzyme res subunit | ||
FPANIOMK_01768 | 2.5e-56 | S | SIR2-like domain | |||
FPANIOMK_01769 | 6.5e-252 | S | AAA-like domain | |||
FPANIOMK_01770 | 0.0 | S | Protein of unknown function DUF262 | |||
FPANIOMK_01771 | 2.8e-28 | |||||
FPANIOMK_01772 | 6.1e-25 | rarD | 3.4.17.13 | E | Rard protein | |
FPANIOMK_01773 | 4.7e-137 | L | IstB-like ATP binding protein | |||
FPANIOMK_01774 | 2.6e-91 | L | Transposase | |||
FPANIOMK_01775 | 1.6e-163 | L | Transposase | |||
FPANIOMK_01776 | 7.3e-59 | rarD | 3.4.17.13 | E | Rard protein | |
FPANIOMK_01777 | 5.3e-23 | rarD | S | Rard protein | ||
FPANIOMK_01778 | 2.7e-179 | I | alpha/beta hydrolase fold | |||
FPANIOMK_01779 | 3.3e-208 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
FPANIOMK_01780 | 3.4e-100 | sixA | T | Phosphoglycerate mutase family | ||
FPANIOMK_01781 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
FPANIOMK_01782 | 4e-161 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
FPANIOMK_01784 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
FPANIOMK_01785 | 1.4e-181 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
FPANIOMK_01786 | 2e-73 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
FPANIOMK_01787 | 8.5e-281 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
FPANIOMK_01788 | 6.8e-181 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
FPANIOMK_01789 | 2.5e-155 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
FPANIOMK_01790 | 2.1e-179 | pyrD | 1.3.1.14 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
FPANIOMK_01791 | 1.5e-124 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
FPANIOMK_01792 | 1e-16 | K | MerR family regulatory protein | |||
FPANIOMK_01793 | 4.7e-196 | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | ||
FPANIOMK_01794 | 2.5e-145 | |||||
FPANIOMK_01796 | 1.9e-15 | KLT | Protein tyrosine kinase | |||
FPANIOMK_01797 | 0.0 | uvrA3 | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
FPANIOMK_01798 | 4.4e-242 | vbsD | V | MatE | ||
FPANIOMK_01799 | 7.3e-132 | S | Enoyl-(Acyl carrier protein) reductase | |||
FPANIOMK_01800 | 2.3e-133 | magIII | L | endonuclease III | ||
FPANIOMK_01801 | 1e-93 | laaE | K | Transcriptional regulator PadR-like family | ||
FPANIOMK_01802 | 1.5e-175 | S | Membrane transport protein | |||
FPANIOMK_01803 | 1.2e-66 | 4.1.1.44 | S | Cupin domain | ||
FPANIOMK_01804 | 2e-224 | hipA | 2.7.11.1 | S | HipA N-terminal domain | |
FPANIOMK_01805 | 3.7e-41 | K | Helix-turn-helix | |||
FPANIOMK_01806 | 1.7e-47 | tam | 2.1.1.144, 2.1.1.197 | FG | trans-aconitate 2-methyltransferase activity | |
FPANIOMK_01807 | 3.5e-18 | |||||
FPANIOMK_01808 | 4.2e-101 | K | Bacterial regulatory proteins, tetR family | |||
FPANIOMK_01809 | 9.6e-86 | T | Domain of unknown function (DUF4234) | |||
FPANIOMK_01810 | 1.2e-171 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
FPANIOMK_01811 | 1.5e-123 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
FPANIOMK_01812 | 0.0 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
FPANIOMK_01813 | 1.4e-141 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
FPANIOMK_01814 | 6.8e-120 | dkgB | S | Oxidoreductase, aldo keto reductase family protein | ||
FPANIOMK_01816 | 5.1e-289 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
FPANIOMK_01817 | 0.0 | pafB | K | WYL domain | ||
FPANIOMK_01818 | 1e-51 | |||||
FPANIOMK_01819 | 0.0 | helY | L | DEAD DEAH box helicase | ||
FPANIOMK_01820 | 3e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
FPANIOMK_01821 | 1.6e-142 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
FPANIOMK_01824 | 3.6e-90 | K | Putative zinc ribbon domain | |||
FPANIOMK_01825 | 7.2e-126 | S | GyrI-like small molecule binding domain | |||
FPANIOMK_01826 | 3.3e-24 | L | DNA integration | |||
FPANIOMK_01827 | 3e-15 | |||||
FPANIOMK_01828 | 1.2e-61 | |||||
FPANIOMK_01829 | 4e-119 | K | helix_turn_helix, mercury resistance | |||
FPANIOMK_01830 | 9.6e-74 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
FPANIOMK_01831 | 1.2e-141 | S | Bacterial protein of unknown function (DUF881) | |||
FPANIOMK_01832 | 9.6e-21 | sbp | S | Protein of unknown function (DUF1290) | ||
FPANIOMK_01833 | 1.8e-173 | S | Bacterial protein of unknown function (DUF881) | |||
FPANIOMK_01834 | 1.8e-116 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
FPANIOMK_01835 | 1.8e-156 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
FPANIOMK_01836 | 6.4e-41 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
FPANIOMK_01837 | 6.3e-101 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
FPANIOMK_01838 | 6.7e-192 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
FPANIOMK_01839 | 6.4e-162 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
FPANIOMK_01840 | 0.0 | trpB | 4.1.1.48, 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
FPANIOMK_01841 | 0.0 | der | 1.1.1.399, 1.1.1.95, 2.7.4.25 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
FPANIOMK_01842 | 7.5e-146 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
FPANIOMK_01843 | 2e-102 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
FPANIOMK_01844 | 5.7e-30 | |||||
FPANIOMK_01845 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
FPANIOMK_01846 | 1.1e-245 | |||||
FPANIOMK_01847 | 2.4e-167 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
FPANIOMK_01848 | 1.1e-225 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
FPANIOMK_01849 | 5.5e-101 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
FPANIOMK_01850 | 2.6e-44 | yajC | U | Preprotein translocase subunit | ||
FPANIOMK_01851 | 1.8e-201 | 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 | |
FPANIOMK_01852 | 2.5e-104 | 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 | |
FPANIOMK_01854 | 1.8e-99 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
FPANIOMK_01855 | 8.2e-129 | yebC | K | transcriptional regulatory protein | ||
FPANIOMK_01856 | 0.0 | 3.2.1.52 | GH20 | M | Glycosyl hydrolase family 20, catalytic domain | |
FPANIOMK_01857 | 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) | |
FPANIOMK_01858 | 1.7e-250 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
FPANIOMK_01862 | 1.5e-214 | |||||
FPANIOMK_01865 | 2.8e-156 | S | PAC2 family | |||
FPANIOMK_01866 | 5e-168 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
FPANIOMK_01867 | 7.1e-160 | G | Fructosamine kinase | |||
FPANIOMK_01868 | 3.4e-211 | 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 | ||
FPANIOMK_01869 | 4.1e-218 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
FPANIOMK_01870 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
FPANIOMK_01871 | 1e-201 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
FPANIOMK_01872 | 1.1e-142 | yoaK | S | Protein of unknown function (DUF1275) | ||
FPANIOMK_01873 | 9.8e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
FPANIOMK_01876 | 5.2e-243 | mepA_6 | V | MatE | ||
FPANIOMK_01877 | 6.1e-162 | S | Sucrose-6F-phosphate phosphohydrolase | |||
FPANIOMK_01878 | 2.6e-177 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
FPANIOMK_01879 | 8e-33 | secG | U | Preprotein translocase SecG subunit | ||
FPANIOMK_01880 | 5.3e-147 | 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) | |
FPANIOMK_01881 | 2.6e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
FPANIOMK_01882 | 3.1e-173 | whiA | K | May be required for sporulation | ||
FPANIOMK_01883 | 2.6e-177 | rapZ | S | Displays ATPase and GTPase activities | ||
FPANIOMK_01884 | 8.9e-181 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
FPANIOMK_01885 | 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 | ||
FPANIOMK_01886 | 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 | ||
FPANIOMK_01887 | 1e-76 | |||||
FPANIOMK_01888 | 3.1e-58 | V | MacB-like periplasmic core domain | |||
FPANIOMK_01890 | 2.1e-117 | K | Transcriptional regulatory protein, C terminal | |||
FPANIOMK_01891 | 1.1e-240 | qseC | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |
FPANIOMK_01892 | 1.1e-138 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
FPANIOMK_01893 | 8.9e-303 | ybiT | S | ABC transporter | ||
FPANIOMK_01894 | 1.4e-197 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
FPANIOMK_01895 | 1.1e-307 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
FPANIOMK_01896 | 2.8e-207 | mdsC | 2.7.1.162, 2.7.1.39 | S | Phosphotransferase enzyme family | |
FPANIOMK_01897 | 6.4e-218 | GK | ROK family | |||
FPANIOMK_01898 | 6.9e-178 | 2.7.1.2 | GK | ROK family | ||
FPANIOMK_01899 | 1.4e-158 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)