ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LMMNOEIH_00001 | 1.4e-189 | K | Periplasmic binding protein domain | |||
LMMNOEIH_00002 | 5.3e-229 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
LMMNOEIH_00003 | 1.9e-146 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
LMMNOEIH_00004 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
LMMNOEIH_00005 | 8.5e-145 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
LMMNOEIH_00006 | 2.2e-142 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00007 | 6.4e-128 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LMMNOEIH_00008 | 8.9e-32 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LMMNOEIH_00009 | 1.5e-156 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LMMNOEIH_00010 | 2e-77 | 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 | ||
LMMNOEIH_00011 | 2.9e-148 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
LMMNOEIH_00012 | 3.4e-161 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
LMMNOEIH_00013 | 8.9e-168 | ftsE | D | Cell division ATP-binding protein FtsE | ||
LMMNOEIH_00014 | 1.1e-190 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LMMNOEIH_00015 | 1.2e-80 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
LMMNOEIH_00016 | 5.8e-143 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
LMMNOEIH_00017 | 5.4e-250 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
LMMNOEIH_00018 | 1.6e-151 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
LMMNOEIH_00019 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LMMNOEIH_00020 | 1.5e-97 | L | Single-strand binding protein family | |||
LMMNOEIH_00021 | 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 | |
LMMNOEIH_00022 | 7.9e-271 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
LMMNOEIH_00023 | 2.5e-161 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
LMMNOEIH_00024 | 2.2e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
LMMNOEIH_00025 | 2.2e-287 | 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 | |
LMMNOEIH_00026 | 5.8e-195 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
LMMNOEIH_00027 | 3.8e-114 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
LMMNOEIH_00028 | 1.9e-124 | livF | E | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_00029 | 4.8e-151 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
LMMNOEIH_00030 | 5.1e-196 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
LMMNOEIH_00031 | 9.5e-156 | U | Belongs to the binding-protein-dependent transport system permease family | |||
LMMNOEIH_00032 | 1.7e-218 | livK | E | Receptor family ligand binding region | ||
LMMNOEIH_00033 | 3.2e-172 | 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 | |
LMMNOEIH_00034 | 1.4e-190 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LMMNOEIH_00035 | 1.5e-35 | rpmE | J | Binds the 23S rRNA | ||
LMMNOEIH_00037 | 6.8e-226 | xylR | GK | ROK family | ||
LMMNOEIH_00038 | 3.8e-287 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LMMNOEIH_00039 | 2.8e-106 | lacA | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
LMMNOEIH_00040 | 4.8e-08 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
LMMNOEIH_00041 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
LMMNOEIH_00042 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
LMMNOEIH_00043 | 2.3e-159 | MA20_14020 | P | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00044 | 1.7e-185 | MA20_14025 | U | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00045 | 8e-230 | msmE | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | ||
LMMNOEIH_00046 | 2.2e-185 | K | Bacterial regulatory proteins, lacI family | |||
LMMNOEIH_00047 | 0.0 | 3.2.1.37, 3.2.1.55 | GH43,GH51 | G | Belongs to the glycosyl hydrolase 43 family | |
LMMNOEIH_00048 | 8.7e-267 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
LMMNOEIH_00049 | 1.2e-249 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LMMNOEIH_00050 | 2.4e-270 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LMMNOEIH_00051 | 1.6e-62 | S | Membrane | |||
LMMNOEIH_00052 | 8.3e-35 | S | Membrane | |||
LMMNOEIH_00053 | 1.7e-16 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
LMMNOEIH_00054 | 5.8e-95 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LMMNOEIH_00055 | 7.6e-56 | xylR | GK | ROK family | ||
LMMNOEIH_00056 | 5.3e-140 | xylR | GK | ROK family | ||
LMMNOEIH_00057 | 5.9e-17 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LMMNOEIH_00058 | 4.6e-129 | xylB | 1.1.1.57, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LMMNOEIH_00059 | 2.3e-167 | F | Inosine-uridine preferring nucleoside hydrolase | |||
LMMNOEIH_00060 | 1.2e-224 | bdhA | C | Iron-containing alcohol dehydrogenase | ||
LMMNOEIH_00061 | 0.0 | 3.1.1.53 | G | Glycosyl hydrolase family 2, sugar binding domain protein | ||
LMMNOEIH_00063 | 1.9e-117 | L | Integrase core domain | |||
LMMNOEIH_00064 | 0.0 | 3.2.1.8 | G | Glycosyl hydrolase family 10 | ||
LMMNOEIH_00065 | 4.6e-229 | 3.2.1.156 | GH8 | G | CBM9 module, glycoside hydrolase family 8 protein and carbohydrate esterase family 4 protein K01238 | |
LMMNOEIH_00066 | 0.0 | O | Highly conserved protein containing a thioredoxin domain | |||
LMMNOEIH_00067 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
LMMNOEIH_00068 | 0.0 | G | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00069 | 4.3e-150 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00070 | 1.4e-173 | U | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00071 | 1.5e-255 | G | ABC transporter periplasmic binding protein YcjN precursor K02027 | |||
LMMNOEIH_00072 | 2.6e-82 | ribD | 1.1.1.193, 3.5.4.26 | H | Cytidine and deoxycytidylate deaminase zinc-binding region | |
LMMNOEIH_00073 | 1.6e-73 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LMMNOEIH_00074 | 1.9e-180 | V | Beta-lactamase | |||
LMMNOEIH_00075 | 0.0 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
LMMNOEIH_00076 | 8.5e-165 | tesB | I | Thioesterase-like superfamily | ||
LMMNOEIH_00077 | 1.8e-93 | S | Protein of unknown function (DUF3180) | |||
LMMNOEIH_00078 | 8.3e-274 | 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 | |
LMMNOEIH_00079 | 1.5e-155 | 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 | |
LMMNOEIH_00080 | 9.6e-115 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
LMMNOEIH_00081 | 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 | ||
LMMNOEIH_00082 | 8.6e-99 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LMMNOEIH_00083 | 2.3e-201 | 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 | |
LMMNOEIH_00084 | 1.1e-232 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
LMMNOEIH_00085 | 6.3e-232 | epsG | M | Glycosyl transferase family 21 | ||
LMMNOEIH_00086 | 2.4e-236 | S | AI-2E family transporter | |||
LMMNOEIH_00087 | 5.5e-180 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
LMMNOEIH_00088 | 1.8e-204 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
LMMNOEIH_00089 | 0.0 | yliE | T | Putative diguanylate phosphodiesterase | ||
LMMNOEIH_00090 | 2.2e-111 | S | Domain of unknown function (DUF4956) | |||
LMMNOEIH_00091 | 1.4e-158 | P | VTC domain | |||
LMMNOEIH_00092 | 3.8e-310 | cotH | M | CotH kinase protein | ||
LMMNOEIH_00093 | 9.9e-275 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
LMMNOEIH_00094 | 1.2e-282 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
LMMNOEIH_00095 | 4e-278 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
LMMNOEIH_00096 | 1e-74 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
LMMNOEIH_00097 | 2.8e-160 | |||||
LMMNOEIH_00098 | 0.0 | 5.1.3.2 | GM | ADP-glyceromanno-heptose 6-epimerase activity | ||
LMMNOEIH_00102 | 6.5e-170 | 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 |
LMMNOEIH_00103 | 9e-200 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LMMNOEIH_00105 | 3.6e-85 | ptpA | 3.1.3.48 | T | low molecular weight | |
LMMNOEIH_00106 | 2.7e-128 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
LMMNOEIH_00107 | 3.8e-181 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
LMMNOEIH_00108 | 2.2e-72 | attW | O | OsmC-like protein | ||
LMMNOEIH_00109 | 5.6e-189 | T | Universal stress protein family | |||
LMMNOEIH_00110 | 1.3e-79 | M | NlpC/P60 family | |||
LMMNOEIH_00111 | 5.6e-164 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LMMNOEIH_00112 | 8.2e-218 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
LMMNOEIH_00113 | 6.2e-41 | |||||
LMMNOEIH_00114 | 1.4e-215 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LMMNOEIH_00115 | 3.3e-89 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LMMNOEIH_00116 | 0.0 | 4.2.1.53 | S | MCRA family | ||
LMMNOEIH_00117 | 3e-139 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LMMNOEIH_00118 | 8.6e-207 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
LMMNOEIH_00119 | 4.1e-99 | S | Serine aminopeptidase, S33 | |||
LMMNOEIH_00120 | 8.8e-251 | G | Psort location CytoplasmicMembrane, score 10.00 | |||
LMMNOEIH_00121 | 2.7e-191 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00122 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LMMNOEIH_00124 | 3.2e-212 | araJ | EGP | Major facilitator Superfamily | ||
LMMNOEIH_00125 | 0.0 | S | Domain of unknown function (DUF4037) | |||
LMMNOEIH_00126 | 4.4e-115 | S | Protein of unknown function (DUF4125) | |||
LMMNOEIH_00127 | 9.3e-93 | |||||
LMMNOEIH_00128 | 1.5e-147 | pspC | KT | PspC domain | ||
LMMNOEIH_00129 | 8.2e-264 | tcsS3 | KT | PspC domain | ||
LMMNOEIH_00130 | 9.3e-36 | degU | K | helix_turn_helix, Lux Regulon | ||
LMMNOEIH_00131 | 3.6e-64 | degU | K | helix_turn_helix, Lux Regulon | ||
LMMNOEIH_00132 | 1.2e-138 | yidP | K | UTRA | ||
LMMNOEIH_00133 | 5.3e-264 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
LMMNOEIH_00134 | 3.6e-274 | eat | E | Amino acid permease | ||
LMMNOEIH_00135 | 2.7e-215 | S | Choline/ethanolamine kinase | |||
LMMNOEIH_00136 | 1.5e-103 | Q | Isochorismatase family | |||
LMMNOEIH_00137 | 1.1e-270 | U | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
LMMNOEIH_00138 | 7.5e-183 | yegV | G | pfkB family carbohydrate kinase | ||
LMMNOEIH_00139 | 2.1e-188 | yegU | O | ADP-ribosylglycohydrolase | ||
LMMNOEIH_00141 | 1.2e-247 | 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) | |
LMMNOEIH_00142 | 9.8e-200 | I | Diacylglycerol kinase catalytic domain | |||
LMMNOEIH_00143 | 1.4e-153 | arbG | K | CAT RNA binding domain | ||
LMMNOEIH_00144 | 0.0 | crr | G | pts system, glucose-specific IIABC component | ||
LMMNOEIH_00145 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
LMMNOEIH_00146 | 2.8e-151 | T | LytTr DNA-binding domain | |||
LMMNOEIH_00147 | 1.5e-250 | T | GHKL domain | |||
LMMNOEIH_00148 | 7.8e-214 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LMMNOEIH_00149 | 2.4e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LMMNOEIH_00151 | 1.9e-107 | |||||
LMMNOEIH_00152 | 1.4e-251 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
LMMNOEIH_00153 | 3.4e-217 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
LMMNOEIH_00154 | 7.3e-187 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
LMMNOEIH_00155 | 2.2e-69 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
LMMNOEIH_00156 | 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 | ||
LMMNOEIH_00157 | 6.1e-191 | nusA | K | Participates in both transcription termination and antitermination | ||
LMMNOEIH_00158 | 2.1e-80 | |||||
LMMNOEIH_00160 | 4.4e-183 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LMMNOEIH_00161 | 1.3e-66 | rplQ | J | Ribosomal protein L17 | ||
LMMNOEIH_00162 | 4.7e-185 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LMMNOEIH_00163 | 1.9e-65 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
LMMNOEIH_00164 | 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 | ||
LMMNOEIH_00165 | 8.4e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LMMNOEIH_00166 | 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 | ||
LMMNOEIH_00167 | 2.5e-98 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
LMMNOEIH_00168 | 3.8e-238 | 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 | ||
LMMNOEIH_00169 | 4.9e-73 | rplO | J | binds to the 23S rRNA | ||
LMMNOEIH_00170 | 3.4e-25 | rpmD | J | Ribosomal protein L30p/L7e | ||
LMMNOEIH_00171 | 1.2e-92 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LMMNOEIH_00172 | 3.3e-59 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
LMMNOEIH_00173 | 3.8e-96 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
LMMNOEIH_00174 | 5.5e-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 | ||
LMMNOEIH_00175 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
LMMNOEIH_00176 | 7.5e-103 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
LMMNOEIH_00177 | 8.7e-51 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LMMNOEIH_00178 | 3e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LMMNOEIH_00179 | 4.9e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LMMNOEIH_00180 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LMMNOEIH_00181 | 1.7e-75 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LMMNOEIH_00182 | 1e-97 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LMMNOEIH_00183 | 1.9e-56 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
LMMNOEIH_00184 | 1.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LMMNOEIH_00185 | 6.1e-154 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
LMMNOEIH_00186 | 6.8e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
LMMNOEIH_00187 | 1.4e-116 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LMMNOEIH_00188 | 2.3e-116 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
LMMNOEIH_00189 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LMMNOEIH_00190 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LMMNOEIH_00191 | 1.1e-181 | rhaR_1 | K | helix_turn_helix, arabinose operon control protein | ||
LMMNOEIH_00192 | 9.5e-197 | Z012_01000 | 1.1.1.14, 1.1.1.9 | C | Zinc-binding dehydrogenase | |
LMMNOEIH_00193 | 9.7e-236 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_00194 | 1.7e-215 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
LMMNOEIH_00195 | 1.4e-76 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
LMMNOEIH_00196 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LMMNOEIH_00197 | 3.4e-67 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LMMNOEIH_00198 | 2.4e-80 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
LMMNOEIH_00199 | 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 |
LMMNOEIH_00200 | 3.1e-122 | |||||
LMMNOEIH_00201 | 2.1e-114 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
LMMNOEIH_00202 | 9.4e-186 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LMMNOEIH_00203 | 4.7e-252 | M | Bacterial capsule synthesis protein PGA_cap | |||
LMMNOEIH_00204 | 9.7e-223 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
LMMNOEIH_00206 | 4.3e-296 | CE10 | I | Belongs to the type-B carboxylesterase lipase family | ||
LMMNOEIH_00207 | 0.0 | G | candidate polyfunctional acetylxylan esterase b-xylosidase A-L-arabinofuranosidase, CBM9 module, glycoside hydrolase family 43 protein and carbohydrate esterase family 6 protein K01238 | |||
LMMNOEIH_00208 | 4.1e-233 | 3.2.1.156 | GH8 | G | CBM9 module, glycoside hydrolase family 8 protein and carbohydrate esterase family 4 protein K01238 | |
LMMNOEIH_00209 | 0.0 | G | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00210 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
LMMNOEIH_00211 | 2.8e-151 | dppF | E | ABC transporter | ||
LMMNOEIH_00212 | 6.7e-156 | oppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
LMMNOEIH_00213 | 3.9e-141 | EP | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00214 | 7.7e-180 | EP | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00215 | 2.5e-247 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LMMNOEIH_00216 | 4.5e-43 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LMMNOEIH_00218 | 2e-211 | dapC | E | Aminotransferase class I and II | ||
LMMNOEIH_00219 | 8.3e-59 | fdxA | C | 4Fe-4S binding domain | ||
LMMNOEIH_00220 | 2.8e-266 | E | aromatic amino acid transport protein AroP K03293 | |||
LMMNOEIH_00221 | 3.4e-206 | murB | 1.3.1.98 | M | Cell wall formation | |
LMMNOEIH_00222 | 5.5e-25 | rpmG | J | Ribosomal protein L33 | ||
LMMNOEIH_00226 | 2.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LMMNOEIH_00227 | 1.8e-146 | |||||
LMMNOEIH_00228 | 2.9e-122 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
LMMNOEIH_00229 | 6.9e-100 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LMMNOEIH_00230 | 6.1e-30 | fmdB | S | Putative regulatory protein | ||
LMMNOEIH_00231 | 1.1e-92 | flgA | NO | SAF | ||
LMMNOEIH_00232 | 3.5e-34 | |||||
LMMNOEIH_00233 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
LMMNOEIH_00234 | 2.1e-175 | T | Forkhead associated domain | |||
LMMNOEIH_00235 | 2.4e-36 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LMMNOEIH_00236 | 1.1e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LMMNOEIH_00237 | 1.3e-246 | pbuO | S | Permease family | ||
LMMNOEIH_00238 | 5.2e-143 | P | Zinc-uptake complex component A periplasmic | |||
LMMNOEIH_00239 | 3e-147 | 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 | |
LMMNOEIH_00240 | 2.2e-166 | pstA | P | Phosphate transport system permease | ||
LMMNOEIH_00241 | 3.4e-164 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LMMNOEIH_00242 | 5.1e-196 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
LMMNOEIH_00243 | 1.3e-128 | KT | Transcriptional regulatory protein, C terminal | |||
LMMNOEIH_00244 | 1.1e-219 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
LMMNOEIH_00245 | 3.6e-123 | 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 | |
LMMNOEIH_00246 | 2.8e-221 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
LMMNOEIH_00247 | 3.3e-211 | 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) | |
LMMNOEIH_00248 | 3.9e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LMMNOEIH_00249 | 2e-59 | D | nuclear chromosome segregation | |||
LMMNOEIH_00250 | 3.4e-126 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
LMMNOEIH_00251 | 2.5e-144 | 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) | |
LMMNOEIH_00252 | 6.9e-184 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
LMMNOEIH_00253 | 7e-297 | yegQ | O | Peptidase family U32 C-terminal domain | ||
LMMNOEIH_00254 | 9.7e-171 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
LMMNOEIH_00255 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
LMMNOEIH_00256 | 1.7e-91 | lemA | S | LemA family | ||
LMMNOEIH_00257 | 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 | |
LMMNOEIH_00258 | 1.7e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LMMNOEIH_00259 | 4.8e-117 | |||||
LMMNOEIH_00261 | 0.0 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
LMMNOEIH_00262 | 1.2e-82 | 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 | |
LMMNOEIH_00264 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LMMNOEIH_00265 | 0.0 | pccB | I | Carboxyl transferase domain | ||
LMMNOEIH_00266 | 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 | |
LMMNOEIH_00267 | 2.1e-79 | bioY | S | BioY family | ||
LMMNOEIH_00268 | 9.5e-161 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
LMMNOEIH_00269 | 0.0 | |||||
LMMNOEIH_00270 | 5e-142 | QT | PucR C-terminal helix-turn-helix domain | |||
LMMNOEIH_00271 | 3e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
LMMNOEIH_00272 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LMMNOEIH_00273 | 1.1e-123 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
LMMNOEIH_00274 | 3.3e-33 | 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 | ||
LMMNOEIH_00276 | 1.4e-231 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
LMMNOEIH_00277 | 1.7e-202 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LMMNOEIH_00278 | 2.3e-311 | 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 | ||
LMMNOEIH_00279 | 2.6e-39 | rpmA | J | Ribosomal L27 protein | ||
LMMNOEIH_00280 | 2.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
LMMNOEIH_00281 | 1.5e-308 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
LMMNOEIH_00282 | 1.5e-230 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
LMMNOEIH_00283 | 2.7e-166 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
LMMNOEIH_00284 | 1.1e-270 | V | Efflux ABC transporter, permease protein | |||
LMMNOEIH_00285 | 5e-128 | V | ATPases associated with a variety of cellular activities | |||
LMMNOEIH_00286 | 2.1e-137 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LMMNOEIH_00287 | 1.1e-123 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LMMNOEIH_00288 | 3e-60 | 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 | ||
LMMNOEIH_00289 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LMMNOEIH_00290 | 5.4e-181 | S | Auxin Efflux Carrier | |||
LMMNOEIH_00293 | 4.7e-190 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_00294 | 7.2e-239 | murN | 2.3.2.16 | V | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_00295 | 1.1e-250 | 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 | |
LMMNOEIH_00296 | 1e-139 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
LMMNOEIH_00297 | 1.4e-119 | 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 | |
LMMNOEIH_00298 | 1.1e-77 | soxR | K | MerR, DNA binding | ||
LMMNOEIH_00299 | 1.7e-195 | yghZ | C | Aldo/keto reductase family | ||
LMMNOEIH_00300 | 7.2e-58 | S | Protein of unknown function (DUF3039) | |||
LMMNOEIH_00301 | 7.7e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LMMNOEIH_00302 | 8.5e-134 | |||||
LMMNOEIH_00303 | 1.8e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
LMMNOEIH_00304 | 1e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LMMNOEIH_00305 | 5.7e-136 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
LMMNOEIH_00306 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
LMMNOEIH_00307 | 4.9e-91 | ilvN | 2.2.1.6 | E | ACT domain | |
LMMNOEIH_00308 | 0.0 | yjjK | S | ABC transporter | ||
LMMNOEIH_00309 | 1.9e-152 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
LMMNOEIH_00310 | 6e-302 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LMMNOEIH_00311 | 2.7e-270 | 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 | |
LMMNOEIH_00312 | 6.8e-179 | S | Endonuclease/Exonuclease/phosphatase family | |||
LMMNOEIH_00313 | 3.9e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LMMNOEIH_00314 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
LMMNOEIH_00315 | 2.4e-107 | 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 | ||
LMMNOEIH_00316 | 1.5e-149 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LMMNOEIH_00317 | 4.5e-98 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
LMMNOEIH_00318 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
LMMNOEIH_00319 | 8.4e-30 | rpmB | J | Ribosomal L28 family | ||
LMMNOEIH_00320 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00321 | 4.1e-229 | yxiO | S | Vacuole effluxer Atg22 like | ||
LMMNOEIH_00322 | 1.9e-127 | gntR | K | FCD | ||
LMMNOEIH_00323 | 1.8e-77 | gntK | 2.7.1.12 | F | Shikimate kinase | |
LMMNOEIH_00324 | 6e-228 | gnuT | EG | GntP family permease | ||
LMMNOEIH_00326 | 5.2e-167 | gnd | 1.1.1.343, 1.1.1.44 | G | 6-phosphogluconate dehydrogenase, C-terminal domain | |
LMMNOEIH_00327 | 4.4e-230 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_00328 | 2.6e-126 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_00329 | 2.4e-228 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LMMNOEIH_00330 | 3.8e-229 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LMMNOEIH_00331 | 1.7e-137 | M | Mechanosensitive ion channel | |||
LMMNOEIH_00332 | 3.3e-179 | S | CAAX protease self-immunity | |||
LMMNOEIH_00333 | 7.5e-214 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
LMMNOEIH_00334 | 2.1e-141 | U | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00335 | 2.7e-158 | U | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00336 | 5.8e-219 | P | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_00337 | 1.2e-219 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
LMMNOEIH_00338 | 1.7e-179 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
LMMNOEIH_00339 | 2.3e-175 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LMMNOEIH_00340 | 1e-256 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LMMNOEIH_00341 | 3.6e-200 | pyrD | 1.3.1.14, 1.3.98.1 | F | Dihydroorotate dehydrogenase | |
LMMNOEIH_00342 | 1.3e-131 | 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 | |
LMMNOEIH_00343 | 7.1e-272 | 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 | |
LMMNOEIH_00344 | 1.1e-139 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
LMMNOEIH_00345 | 5.1e-268 | S | Calcineurin-like phosphoesterase | |||
LMMNOEIH_00348 | 9.3e-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) | |
LMMNOEIH_00349 | 2e-114 | S | Protein of unknown function (DUF805) | |||
LMMNOEIH_00350 | 7e-184 | |||||
LMMNOEIH_00351 | 1.5e-123 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LMMNOEIH_00352 | 2.1e-263 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_00353 | 3.2e-95 | S | GtrA-like protein | |||
LMMNOEIH_00354 | 2.5e-61 | S | Macrophage migration inhibitory factor (MIF) | |||
LMMNOEIH_00355 | 1e-287 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
LMMNOEIH_00356 | 0.0 | pepD | E | Peptidase family C69 | ||
LMMNOEIH_00357 | 2.4e-106 | S | Phosphatidylethanolamine-binding protein | |||
LMMNOEIH_00358 | 1e-285 | 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) | |
LMMNOEIH_00359 | 6e-39 | ptsH | G | PTS HPr component phosphorylation site | ||
LMMNOEIH_00360 | 5.4e-184 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00361 | 3.8e-194 | holB | 2.7.7.7 | L | DNA polymerase III | |
LMMNOEIH_00362 | 1.6e-112 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LMMNOEIH_00363 | 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 | |
LMMNOEIH_00364 | 6.2e-191 | 3.6.1.27 | I | PAP2 superfamily | ||
LMMNOEIH_00365 | 1.7e-234 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
LMMNOEIH_00366 | 7.7e-216 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
LMMNOEIH_00367 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LMMNOEIH_00368 | 0.0 | S | Beta-L-arabinofuranosidase, GH127 | |||
LMMNOEIH_00369 | 4.6e-155 | U | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00370 | 5e-168 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00371 | 2e-244 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_00372 | 1.3e-203 | abf | G | Glycosyl hydrolases family 43 | ||
LMMNOEIH_00373 | 1.1e-195 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00374 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolases family 43 | |
LMMNOEIH_00375 | 0.0 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
LMMNOEIH_00376 | 0.0 | 3.2.1.99 | GH43 | G | C-terminal of Glycosyl hydrolases family 43 | |
LMMNOEIH_00377 | 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) | |
LMMNOEIH_00378 | 4e-295 | S | Calcineurin-like phosphoesterase | |||
LMMNOEIH_00379 | 7.1e-115 | |||||
LMMNOEIH_00380 | 2.7e-48 | yitI | S | Acetyltransferase (GNAT) domain | ||
LMMNOEIH_00381 | 1.8e-209 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
LMMNOEIH_00382 | 1.4e-96 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
LMMNOEIH_00383 | 1.7e-134 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
LMMNOEIH_00384 | 1e-105 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
LMMNOEIH_00385 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
LMMNOEIH_00386 | 1.1e-96 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_00387 | 1.6e-193 | S | Psort location CytoplasmicMembrane, score | |||
LMMNOEIH_00388 | 4.9e-218 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
LMMNOEIH_00389 | 4.7e-56 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
LMMNOEIH_00390 | 5.1e-60 | U | TadE-like protein | |||
LMMNOEIH_00391 | 1.3e-42 | S | Protein of unknown function (DUF4244) | |||
LMMNOEIH_00392 | 2.2e-88 | gspF | NU | Type II secretion system (T2SS), protein F | ||
LMMNOEIH_00393 | 6.9e-125 | U | Type ii secretion system | |||
LMMNOEIH_00394 | 1.8e-184 | cpaF | U | Type II IV secretion system protein | ||
LMMNOEIH_00395 | 5.5e-141 | cpaE | D | bacterial-type flagellum organization | ||
LMMNOEIH_00397 | 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) | |
LMMNOEIH_00398 | 6.2e-207 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
LMMNOEIH_00399 | 6.6e-91 | |||||
LMMNOEIH_00400 | 2.7e-117 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
LMMNOEIH_00401 | 1.8e-206 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
LMMNOEIH_00402 | 0.0 | G | Bacterial Ig-like domain (group 4) | |||
LMMNOEIH_00403 | 0.0 | sca1 | 3.2.1.187 | GH121 | DG | Bacterial Ig-like domain (group 4) |
LMMNOEIH_00404 | 0.0 | 3.2.1.185 | GH127 | S | Beta-L-arabinofuranosidase, GH127 | |
LMMNOEIH_00405 | 9.3e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00406 | 3.1e-167 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00407 | 8.1e-08 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00408 | 1.1e-242 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_00409 | 4.1e-192 | K | Periplasmic binding protein domain | |||
LMMNOEIH_00410 | 0.0 | ubiB | S | ABC1 family | ||
LMMNOEIH_00411 | 1e-27 | S | granule-associated protein | |||
LMMNOEIH_00412 | 3.6e-137 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
LMMNOEIH_00413 | 3.9e-252 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
LMMNOEIH_00414 | 3.3e-248 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LMMNOEIH_00415 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
LMMNOEIH_00416 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
LMMNOEIH_00417 | 1.2e-236 | amt | U | Ammonium Transporter Family | ||
LMMNOEIH_00418 | 8.6e-168 | 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) | ||
LMMNOEIH_00419 | 4.9e-108 | icaR | K | Bacterial regulatory proteins, tetR family | ||
LMMNOEIH_00420 | 4e-195 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
LMMNOEIH_00421 | 1.7e-304 | pepD | E | Peptidase family C69 | ||
LMMNOEIH_00423 | 6e-38 | nrdH | O | Glutaredoxin | ||
LMMNOEIH_00424 | 2.9e-224 | S | Putative ABC-transporter type IV | |||
LMMNOEIH_00425 | 0.0 | pip | S | YhgE Pip domain protein | ||
LMMNOEIH_00426 | 4.4e-276 | pip | S | YhgE Pip domain protein | ||
LMMNOEIH_00427 | 7.8e-88 | K | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00428 | 1.1e-61 | S | FMN_bind | |||
LMMNOEIH_00429 | 1e-148 | macB | V | ABC transporter, ATP-binding protein | ||
LMMNOEIH_00430 | 1.6e-201 | Z012_06715 | V | FtsX-like permease family | ||
LMMNOEIH_00432 | 1.1e-219 | macB_2 | V | ABC transporter permease | ||
LMMNOEIH_00433 | 6.1e-230 | S | Predicted membrane protein (DUF2318) | |||
LMMNOEIH_00434 | 1.2e-91 | tpd | P | Fe2+ transport protein | ||
LMMNOEIH_00435 | 3e-299 | efeU_1 | P | Iron permease FTR1 family | ||
LMMNOEIH_00436 | 4.4e-237 | G | MFS/sugar transport protein | |||
LMMNOEIH_00437 | 5.8e-116 | 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 | |
LMMNOEIH_00438 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
LMMNOEIH_00439 | 2.1e-285 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
LMMNOEIH_00440 | 1.9e-57 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
LMMNOEIH_00441 | 6.1e-183 | 1.1.1.65 | C | Aldo/keto reductase family | ||
LMMNOEIH_00442 | 2.5e-26 | thiS | 2.8.1.10 | H | ThiS family | |
LMMNOEIH_00443 | 3.8e-128 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
LMMNOEIH_00444 | 1.2e-166 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
LMMNOEIH_00445 | 9.9e-275 | cycA | E | Amino acid permease | ||
LMMNOEIH_00446 | 1.5e-18 | |||||
LMMNOEIH_00447 | 4.3e-79 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00448 | 1.5e-251 | M | domain protein | |||
LMMNOEIH_00449 | 0.0 | inlJ | M | domain protein | ||
LMMNOEIH_00450 | 3.1e-176 | 3.4.22.70 | M | Sortase family | ||
LMMNOEIH_00451 | 5e-79 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00452 | 3.3e-227 | P | Sodium/hydrogen exchanger family | |||
LMMNOEIH_00453 | 0.0 | V | FtsX-like permease family | |||
LMMNOEIH_00454 | 5.4e-270 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
LMMNOEIH_00455 | 2.4e-11 | S | Protein of unknown function, DUF624 | |||
LMMNOEIH_00456 | 7.3e-189 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00457 | 4.9e-39 | G | beta-mannosidase | |||
LMMNOEIH_00458 | 0.0 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
LMMNOEIH_00459 | 1.2e-202 | 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 | |
LMMNOEIH_00460 | 1.8e-203 | 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 | |
LMMNOEIH_00461 | 1e-251 | yhjE | EGP | Sugar (and other) transporter | ||
LMMNOEIH_00462 | 3.7e-269 | scrT | G | Transporter major facilitator family protein | ||
LMMNOEIH_00463 | 1.6e-149 | amyC5 | P | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00464 | 2.9e-162 | amyD3 | P | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00465 | 1.5e-223 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_00466 | 0.0 | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain | |
LMMNOEIH_00467 | 1.5e-115 | S | Protein of unknown function, DUF624 | |||
LMMNOEIH_00468 | 2.6e-296 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
LMMNOEIH_00469 | 3.2e-195 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00470 | 1.4e-29 | E | Receptor family ligand binding region | |||
LMMNOEIH_00471 | 3.3e-57 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LMMNOEIH_00472 | 3.7e-155 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LMMNOEIH_00473 | 4.7e-296 | clcA | P | Voltage gated chloride channel | ||
LMMNOEIH_00474 | 1.6e-249 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
LMMNOEIH_00475 | 4.1e-206 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
LMMNOEIH_00476 | 0.0 | pip | S | YhgE Pip domain protein | ||
LMMNOEIH_00477 | 0.0 | pip | S | YhgE Pip domain protein | ||
LMMNOEIH_00478 | 9.1e-170 | yddG | EG | EamA-like transporter family | ||
LMMNOEIH_00479 | 5.5e-65 | K | Helix-turn-helix XRE-family like proteins | |||
LMMNOEIH_00481 | 3.2e-163 | htpX | O | Belongs to the peptidase M48B family | ||
LMMNOEIH_00482 | 3.4e-269 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LMMNOEIH_00483 | 7.9e-188 | ansA | 3.5.1.1 | EJ | Asparaginase | |
LMMNOEIH_00484 | 0.0 | cadA | P | E1-E2 ATPase | ||
LMMNOEIH_00485 | 1.7e-226 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
LMMNOEIH_00486 | 4.1e-264 | 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) | |
LMMNOEIH_00488 | 3.3e-10 | XK27_10430 | S | NAD(P)H-binding | ||
LMMNOEIH_00489 | 8.8e-160 | yicL | EG | EamA-like transporter family | ||
LMMNOEIH_00490 | 6e-194 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
LMMNOEIH_00491 | 7.1e-113 | K | helix_turn_helix, Lux Regulon | |||
LMMNOEIH_00492 | 1.9e-226 | 2.7.13.3 | T | Histidine kinase | ||
LMMNOEIH_00493 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
LMMNOEIH_00494 | 1.2e-131 | fhaA | T | Protein of unknown function (DUF2662) | ||
LMMNOEIH_00495 | 9.6e-73 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LMMNOEIH_00496 | 1.3e-240 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
LMMNOEIH_00497 | 7.9e-264 | rodA | D | Belongs to the SEDS family | ||
LMMNOEIH_00498 | 8e-266 | pbpA | M | penicillin-binding protein | ||
LMMNOEIH_00499 | 5.8e-177 | T | Protein tyrosine kinase | |||
LMMNOEIH_00500 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
LMMNOEIH_00501 | 1.7e-119 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
LMMNOEIH_00502 | 2.1e-207 | srtA | 3.4.22.70 | M | Sortase family | |
LMMNOEIH_00503 | 6.8e-142 | S | Bacterial protein of unknown function (DUF881) | |||
LMMNOEIH_00504 | 3.1e-57 | crgA | D | Involved in cell division | ||
LMMNOEIH_00505 | 1e-238 | L | ribosomal rna small subunit methyltransferase | |||
LMMNOEIH_00506 | 6.3e-148 | gluP | 3.4.21.105 | S | Rhomboid family | |
LMMNOEIH_00507 | 1.5e-35 | |||||
LMMNOEIH_00508 | 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 |
LMMNOEIH_00509 | 6.3e-63 | I | Sterol carrier protein | |||
LMMNOEIH_00510 | 4.9e-42 | S | Protein of unknown function (DUF3073) | |||
LMMNOEIH_00511 | 5.9e-205 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LMMNOEIH_00512 | 9.4e-300 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
LMMNOEIH_00513 | 0.0 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LMMNOEIH_00514 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LMMNOEIH_00515 | 4.3e-66 | |||||
LMMNOEIH_00516 | 1.1e-38 | |||||
LMMNOEIH_00517 | 2e-118 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LMMNOEIH_00518 | 2.8e-241 | ytfL | P | Transporter associated domain | ||
LMMNOEIH_00519 | 2.1e-185 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
LMMNOEIH_00520 | 1.7e-99 | S | Protein of unknown function DUF45 | |||
LMMNOEIH_00524 | 2.5e-57 | 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 | ||
LMMNOEIH_00525 | 1.2e-260 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LMMNOEIH_00526 | 9.6e-68 | S | Transmembrane domain of unknown function (DUF3566) | |||
LMMNOEIH_00527 | 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 | |
LMMNOEIH_00528 | 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 | |
LMMNOEIH_00529 | 5.3e-89 | S | Protein of unknown function (DUF721) | |||
LMMNOEIH_00530 | 2.4e-234 | 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 | ||
LMMNOEIH_00531 | 3e-204 | 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 | |
LMMNOEIH_00532 | 2.9e-306 | 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 | ||
LMMNOEIH_00533 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
LMMNOEIH_00534 | 1.5e-43 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
LMMNOEIH_00535 | 1.9e-189 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
LMMNOEIH_00536 | 3.6e-91 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
LMMNOEIH_00537 | 2.7e-127 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
LMMNOEIH_00538 | 4.5e-172 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LMMNOEIH_00539 | 3.1e-203 | parB | K | Belongs to the ParB family | ||
LMMNOEIH_00540 | 3.1e-181 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LMMNOEIH_00541 | 7e-14 | S | Psort location Extracellular, score 8.82 | |||
LMMNOEIH_00543 | 1.4e-121 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
LMMNOEIH_00544 | 2e-12 | S | Domain of unknown function (DUF4143) | |||
LMMNOEIH_00545 | 0.0 | murJ | KLT | MviN-like protein | ||
LMMNOEIH_00546 | 4.1e-306 | murJ | KLT | MviN-like protein | ||
LMMNOEIH_00547 | 0.0 | M | Conserved repeat domain | |||
LMMNOEIH_00548 | 6.3e-122 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
LMMNOEIH_00549 | 6.5e-284 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
LMMNOEIH_00550 | 2.6e-109 | S | LytR cell envelope-related transcriptional attenuator | |||
LMMNOEIH_00551 | 6.2e-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 | |
LMMNOEIH_00552 | 2e-166 | 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 | |
LMMNOEIH_00553 | 2.1e-197 | S | G5 | |||
LMMNOEIH_00555 | 7.5e-151 | O | Thioredoxin | |||
LMMNOEIH_00556 | 0.0 | KLT | Protein tyrosine kinase | |||
LMMNOEIH_00557 | 0.0 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
LMMNOEIH_00558 | 3.4e-140 | I | alpha/beta hydrolase fold | |||
LMMNOEIH_00559 | 1.1e-30 | I | alpha/beta hydrolase fold | |||
LMMNOEIH_00560 | 1e-144 | cobB2 | K | Sir2 family | ||
LMMNOEIH_00561 | 2.6e-233 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
LMMNOEIH_00562 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
LMMNOEIH_00563 | 2.6e-155 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00564 | 6.6e-157 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00565 | 1.5e-244 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
LMMNOEIH_00566 | 7.6e-230 | nagC | GK | ROK family | ||
LMMNOEIH_00567 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
LMMNOEIH_00568 | 4.5e-76 | 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) | |
LMMNOEIH_00569 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
LMMNOEIH_00570 | 1.2e-154 | ypfH | S | Phospholipase/Carboxylesterase | ||
LMMNOEIH_00571 | 4e-112 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
LMMNOEIH_00572 | 1.5e-94 | T | Diguanylate cyclase (GGDEF) domain protein | |||
LMMNOEIH_00573 | 2.1e-116 | L | Protein of unknown function (DUF1524) | |||
LMMNOEIH_00574 | 8.4e-167 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
LMMNOEIH_00575 | 2.1e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LMMNOEIH_00576 | 1.1e-195 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00577 | 0.0 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_00578 | 9.2e-107 | G | ABC transporter permease | |||
LMMNOEIH_00580 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
LMMNOEIH_00581 | 1.7e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
LMMNOEIH_00582 | 1e-166 | G | ABC transporter permease | |||
LMMNOEIH_00583 | 9.5e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_00584 | 9.3e-108 | L | Transposase and inactivated derivatives | |||
LMMNOEIH_00585 | 3.8e-29 | L | transposase activity | |||
LMMNOEIH_00586 | 2.2e-137 | T | Diguanylate cyclase (GGDEF) domain protein | |||
LMMNOEIH_00587 | 1.9e-247 | S | zinc finger | |||
LMMNOEIH_00588 | 7.5e-71 | S | Bacterial PH domain | |||
LMMNOEIH_00589 | 1.5e-76 | |||||
LMMNOEIH_00590 | 1.3e-198 | V | Domain of unknown function (DUF3427) | |||
LMMNOEIH_00591 | 0.0 | helD | 3.6.4.12 | L | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_00592 | 8.1e-185 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
LMMNOEIH_00593 | 1.5e-70 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LMMNOEIH_00594 | 1.4e-231 | aspB | E | Aminotransferase class-V | ||
LMMNOEIH_00595 | 2.9e-179 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LMMNOEIH_00596 | 6.1e-126 | tmp1 | S | Domain of unknown function (DUF4391) | ||
LMMNOEIH_00597 | 6.2e-199 | S | Endonuclease/Exonuclease/phosphatase family | |||
LMMNOEIH_00599 | 7e-41 | 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 | |
LMMNOEIH_00600 | 8.9e-245 | 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 | |
LMMNOEIH_00601 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
LMMNOEIH_00602 | 1.6e-139 | 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 | |
LMMNOEIH_00603 | 3.9e-156 | hgdC | I | BadF/BadG/BcrA/BcrD ATPase family | ||
LMMNOEIH_00604 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LMMNOEIH_00605 | 5.5e-255 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
LMMNOEIH_00606 | 5.7e-120 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_00607 | 0.0 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
LMMNOEIH_00608 | 1.7e-111 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_00609 | 1.9e-218 | G | Transporter major facilitator family protein | |||
LMMNOEIH_00611 | 1.2e-271 | srfJ1 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain |
LMMNOEIH_00613 | 2.6e-20 | Q | Belongs to the P-Pant transferase superfamily | |||
LMMNOEIH_00614 | 2e-130 | ydjE | EGP | Major facilitator Superfamily | ||
LMMNOEIH_00615 | 1.9e-209 | hsvB | 6.3.2.4 | M | Belongs to the D-alanine--D-alanine ligase family | |
LMMNOEIH_00616 | 7e-75 | mcyA | Q | Nodulation protein S (NodS) | ||
LMMNOEIH_00617 | 9.3e-199 | P | Major Facilitator Superfamily | |||
LMMNOEIH_00618 | 8.9e-247 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
LMMNOEIH_00619 | 0.0 | 3.2.1.37 | GH43 | G | Glycosyl hydrolases family 43 | |
LMMNOEIH_00620 | 1.1e-239 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
LMMNOEIH_00621 | 2.3e-108 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_00622 | 0.0 | bgl2 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain |
LMMNOEIH_00623 | 8e-221 | lmrB | U | Major Facilitator Superfamily | ||
LMMNOEIH_00624 | 1.5e-14 | K | helix_turn_helix, mercury resistance | |||
LMMNOEIH_00625 | 3.8e-87 | K | Periplasmic binding protein domain | |||
LMMNOEIH_00626 | 5.4e-151 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_00627 | 0.0 | 3.2.1.40 | E | Bacterial alpha-L-rhamnosidase C-terminal domain | ||
LMMNOEIH_00628 | 7.9e-180 | G | Transporter major facilitator family protein | |||
LMMNOEIH_00629 | 8.4e-197 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
LMMNOEIH_00630 | 9.6e-106 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_00631 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
LMMNOEIH_00632 | 4.6e-97 | K | MarR family | |||
LMMNOEIH_00633 | 0.0 | V | ABC transporter, ATP-binding protein | |||
LMMNOEIH_00634 | 0.0 | V | ABC transporter transmembrane region | |||
LMMNOEIH_00635 | 8.1e-185 | lacR | K | Transcriptional regulator, LacI family | ||
LMMNOEIH_00636 | 1e-257 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
LMMNOEIH_00637 | 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) | |
LMMNOEIH_00638 | 0.0 | cas9 | 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). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
LMMNOEIH_00639 | 3.7e-165 | 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 | ||
LMMNOEIH_00640 | 6e-18 | 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 | ||
LMMNOEIH_00641 | 3.4e-115 | S | CRISPR-associated protein (Cas_Csn2) | |||
LMMNOEIH_00642 | 1e-130 | L | PFAM Integrase catalytic | |||
LMMNOEIH_00643 | 7.3e-33 | |||||
LMMNOEIH_00645 | 1.1e-124 | S | Phospholipase/Carboxylesterase | |||
LMMNOEIH_00646 | 2.4e-239 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LMMNOEIH_00647 | 3.9e-187 | K | LysR substrate binding domain protein | |||
LMMNOEIH_00648 | 3.2e-155 | S | Patatin-like phospholipase | |||
LMMNOEIH_00649 | 1.9e-175 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
LMMNOEIH_00650 | 7.8e-302 | E | ABC transporter, substrate-binding protein, family 5 | |||
LMMNOEIH_00651 | 3.5e-21 | S | Patatin-like phospholipase | |||
LMMNOEIH_00652 | 2.2e-145 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LMMNOEIH_00653 | 7.8e-171 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine | |
LMMNOEIH_00654 | 5.3e-116 | S | Vitamin K epoxide reductase | |||
LMMNOEIH_00655 | 3.3e-172 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
LMMNOEIH_00656 | 3.6e-32 | S | Protein of unknown function (DUF3107) | |||
LMMNOEIH_00657 | 1.8e-268 | mphA | S | Aminoglycoside phosphotransferase | ||
LMMNOEIH_00658 | 1.6e-282 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
LMMNOEIH_00659 | 2.7e-283 | S | Zincin-like metallopeptidase | |||
LMMNOEIH_00660 | 1e-154 | lon | T | Belongs to the peptidase S16 family | ||
LMMNOEIH_00661 | 6.5e-75 | S | Protein of unknown function (DUF3052) | |||
LMMNOEIH_00663 | 8.9e-239 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
LMMNOEIH_00664 | 8.5e-218 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
LMMNOEIH_00665 | 5.6e-225 | 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 | |
LMMNOEIH_00666 | 0.0 | I | acetylesterase activity | |||
LMMNOEIH_00667 | 7.3e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LMMNOEIH_00668 | 4.5e-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 | |
LMMNOEIH_00669 | 3.2e-218 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
LMMNOEIH_00670 | 5.3e-206 | P | NMT1/THI5 like | |||
LMMNOEIH_00671 | 1.4e-142 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
LMMNOEIH_00672 | 0.0 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LMMNOEIH_00673 | 2.8e-241 | lacY | P | LacY proton/sugar symporter | ||
LMMNOEIH_00674 | 1.1e-192 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_00675 | 3e-60 | S | Thiamine-binding protein | |||
LMMNOEIH_00676 | 2.9e-151 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
LMMNOEIH_00677 | 2e-132 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
LMMNOEIH_00678 | 2.2e-154 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
LMMNOEIH_00679 | 1.3e-295 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
LMMNOEIH_00680 | 2.5e-244 | 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 | ||
LMMNOEIH_00681 | 5.6e-220 | 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 | ||
LMMNOEIH_00682 | 8.9e-81 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
LMMNOEIH_00683 | 1.2e-40 | yggT | S | YGGT family | ||
LMMNOEIH_00684 | 4.5e-31 | 3.1.21.3 | V | DivIVA protein | ||
LMMNOEIH_00685 | 4.3e-87 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LMMNOEIH_00686 | 4.9e-176 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LMMNOEIH_00687 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
LMMNOEIH_00688 | 2.4e-259 | 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 | |
LMMNOEIH_00689 | 2.5e-225 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LMMNOEIH_00690 | 1.5e-109 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
LMMNOEIH_00691 | 1.5e-122 | |||||
LMMNOEIH_00692 | 6.3e-122 | 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 | ||
LMMNOEIH_00693 | 3.1e-130 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
LMMNOEIH_00694 | 3.1e-264 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
LMMNOEIH_00695 | 5.6e-219 | S | Domain of unknown function (DUF5067) | |||
LMMNOEIH_00696 | 3.6e-139 | M | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses | |||
LMMNOEIH_00697 | 3.2e-220 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_00698 | 5e-119 | ytrE | V | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_00699 | 9.2e-82 | |||||
LMMNOEIH_00700 | 1.6e-183 | V | N-Acetylmuramoyl-L-alanine amidase | |||
LMMNOEIH_00701 | 4.7e-191 | |||||
LMMNOEIH_00702 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
LMMNOEIH_00703 | 2.9e-113 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
LMMNOEIH_00704 | 1.9e-270 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LMMNOEIH_00705 | 2.3e-176 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
LMMNOEIH_00706 | 1.3e-149 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
LMMNOEIH_00707 | 2.2e-131 | 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 | |
LMMNOEIH_00708 | 2.3e-53 | M | Lysin motif | |||
LMMNOEIH_00709 | 8.5e-84 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LMMNOEIH_00710 | 1.1e-217 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
LMMNOEIH_00711 | 0.0 | L | DNA helicase | |||
LMMNOEIH_00712 | 7e-92 | mraZ | K | Belongs to the MraZ family | ||
LMMNOEIH_00713 | 1.3e-190 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LMMNOEIH_00714 | 6.7e-62 | 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 | ||
LMMNOEIH_00715 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
LMMNOEIH_00716 | 1.1e-153 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
LMMNOEIH_00717 | 6.4e-263 | 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 | |
LMMNOEIH_00718 | 8.8e-193 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LMMNOEIH_00719 | 6.2e-255 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LMMNOEIH_00720 | 8.1e-203 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
LMMNOEIH_00721 | 6.3e-216 | 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) |
LMMNOEIH_00722 | 2.3e-271 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
LMMNOEIH_00723 | 1.7e-140 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
LMMNOEIH_00724 | 8.4e-248 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
LMMNOEIH_00725 | 1.6e-27 | |||||
LMMNOEIH_00726 | 3.5e-220 | S | Metal-independent alpha-mannosidase (GH125) | |||
LMMNOEIH_00727 | 1.1e-164 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
LMMNOEIH_00728 | 1.7e-218 | GK | ROK family | |||
LMMNOEIH_00729 | 6.1e-307 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
LMMNOEIH_00730 | 1.7e-188 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00731 | 4.7e-192 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00732 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
LMMNOEIH_00733 | 9e-95 | 3.6.1.55 | F | NUDIX domain | ||
LMMNOEIH_00734 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
LMMNOEIH_00735 | 3.7e-288 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
LMMNOEIH_00736 | 3.5e-188 | V | Acetyltransferase (GNAT) domain | |||
LMMNOEIH_00737 | 3.3e-278 | 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 | |
LMMNOEIH_00738 | 1.7e-97 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
LMMNOEIH_00739 | 1.2e-36 | |||||
LMMNOEIH_00740 | 4.3e-188 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
LMMNOEIH_00741 | 7.9e-172 | 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 | |
LMMNOEIH_00742 | 2.1e-88 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
LMMNOEIH_00743 | 1.8e-198 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LMMNOEIH_00744 | 4.9e-110 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
LMMNOEIH_00745 | 1.6e-103 | 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 | ||
LMMNOEIH_00746 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
LMMNOEIH_00747 | 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 | ||
LMMNOEIH_00748 | 2e-177 | xerD | D | recombinase XerD | ||
LMMNOEIH_00749 | 6.8e-153 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LMMNOEIH_00750 | 2.1e-151 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
LMMNOEIH_00751 | 2.6e-250 | naiP | U | Sugar (and other) transporter | ||
LMMNOEIH_00752 | 0.0 | typA | T | Elongation factor G C-terminus | ||
LMMNOEIH_00753 | 4e-104 | |||||
LMMNOEIH_00754 | 1.3e-190 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
LMMNOEIH_00755 | 8.9e-195 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
LMMNOEIH_00756 | 2.8e-34 | |||||
LMMNOEIH_00757 | 5.2e-08 | |||||
LMMNOEIH_00758 | 1.6e-171 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
LMMNOEIH_00759 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
LMMNOEIH_00760 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
LMMNOEIH_00761 | 1.6e-155 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00762 | 4.1e-170 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
LMMNOEIH_00763 | 0.0 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
LMMNOEIH_00764 | 1.4e-172 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
LMMNOEIH_00765 | 1.7e-151 | S | Protein of unknown function (DUF3710) | |||
LMMNOEIH_00766 | 2.4e-133 | S | Protein of unknown function (DUF3159) | |||
LMMNOEIH_00767 | 2.8e-243 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LMMNOEIH_00768 | 2e-74 | |||||
LMMNOEIH_00769 | 0.0 | ctpE | P | E1-E2 ATPase | ||
LMMNOEIH_00770 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
LMMNOEIH_00771 | 2.9e-249 | VP1224 | V | Psort location CytoplasmicMembrane, score 9.99 | ||
LMMNOEIH_00772 | 4.7e-109 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
LMMNOEIH_00773 | 2.2e-209 | rhaR1 | K | helix_turn_helix, arabinose operon control protein | ||
LMMNOEIH_00774 | 1.1e-229 | V | ABC-2 family transporter protein | |||
LMMNOEIH_00775 | 7.7e-225 | V | ABC-2 family transporter protein | |||
LMMNOEIH_00776 | 4.4e-191 | V | ATPases associated with a variety of cellular activities | |||
LMMNOEIH_00777 | 4.6e-244 | T | Histidine kinase | |||
LMMNOEIH_00778 | 9e-116 | K | helix_turn_helix, Lux Regulon | |||
LMMNOEIH_00779 | 0.0 | S | Protein of unknown function DUF262 | |||
LMMNOEIH_00780 | 1.8e-127 | K | helix_turn_helix, Lux Regulon | |||
LMMNOEIH_00781 | 3.3e-242 | T | Histidine kinase | |||
LMMNOEIH_00782 | 1.4e-57 | S | Domain of unknown function (DUF5067) | |||
LMMNOEIH_00783 | 1.7e-127 | ybhL | S | Belongs to the BI1 family | ||
LMMNOEIH_00784 | 8e-177 | ydeD | EG | EamA-like transporter family | ||
LMMNOEIH_00785 | 1.1e-155 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
LMMNOEIH_00786 | 8.7e-281 | 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 | |
LMMNOEIH_00787 | 6e-191 | 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) | |
LMMNOEIH_00788 | 7.2e-11 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
LMMNOEIH_00789 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
LMMNOEIH_00790 | 4.1e-124 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LMMNOEIH_00791 | 6.1e-97 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LMMNOEIH_00792 | 1.6e-80 | K | Helix-turn-helix XRE-family like proteins | |||
LMMNOEIH_00793 | 4.3e-46 | S | Protein of unknown function (DUF3046) | |||
LMMNOEIH_00794 | 5.4e-212 | 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 | ||
LMMNOEIH_00795 | 6.6e-122 | recX | S | Modulates RecA activity | ||
LMMNOEIH_00796 | 3.3e-118 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LMMNOEIH_00797 | 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 | ||
LMMNOEIH_00798 | 3.4e-194 | 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) | |
LMMNOEIH_00799 | 1.3e-97 | |||||
LMMNOEIH_00800 | 1.9e-132 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LMMNOEIH_00801 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
LMMNOEIH_00802 | 9.1e-198 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
LMMNOEIH_00803 | 1.1e-118 | |||||
LMMNOEIH_00804 | 3.4e-173 | 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 | ||
LMMNOEIH_00805 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LMMNOEIH_00806 | 1.5e-222 | G | Major Facilitator Superfamily | |||
LMMNOEIH_00807 | 5.6e-242 | T | PhoQ Sensor | |||
LMMNOEIH_00808 | 2.4e-79 | S | Protein of unknown function (DUF2975) | |||
LMMNOEIH_00809 | 5.8e-32 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
LMMNOEIH_00810 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
LMMNOEIH_00811 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LMMNOEIH_00812 | 3e-234 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
LMMNOEIH_00813 | 4.1e-147 | S | Protein of unknown function (DUF3071) | |||
LMMNOEIH_00814 | 1e-47 | S | Domain of unknown function (DUF4193) | |||
LMMNOEIH_00815 | 1.3e-84 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
LMMNOEIH_00816 | 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 | |
LMMNOEIH_00817 | 1.2e-102 | 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 | |
LMMNOEIH_00818 | 4.1e-243 | dinF | V | MatE | ||
LMMNOEIH_00819 | 0.0 | S | LPXTG-motif cell wall anchor domain protein | |||
LMMNOEIH_00820 | 5.1e-113 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LMMNOEIH_00822 | 3.7e-150 | metQ | P | NLPA lipoprotein | ||
LMMNOEIH_00823 | 2.5e-174 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LMMNOEIH_00824 | 1.3e-93 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_00825 | 1.2e-211 | S | Peptidase dimerisation domain | |||
LMMNOEIH_00826 | 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 | |
LMMNOEIH_00827 | 4.5e-31 | |||||
LMMNOEIH_00828 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
LMMNOEIH_00829 | 7.4e-166 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
LMMNOEIH_00830 | 9.9e-80 | S | Protein of unknown function (DUF3000) | |||
LMMNOEIH_00831 | 2.6e-236 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
LMMNOEIH_00832 | 1.2e-231 | 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 | ||
LMMNOEIH_00833 | 5.5e-130 | yebE | S | DUF218 domain | ||
LMMNOEIH_00834 | 8.4e-128 | E | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00835 | 3e-159 | O | Thioredoxin | |||
LMMNOEIH_00836 | 1.2e-158 | msbA2 | 3.6.3.44 | V | ABC transporter transmembrane region | |
LMMNOEIH_00837 | 4.2e-138 | 3.6.3.44 | V | ABC transporter | ||
LMMNOEIH_00838 | 0.0 | KLT | Lanthionine synthetase C-like protein | |||
LMMNOEIH_00839 | 3.2e-121 | K | helix_turn_helix, Lux Regulon | |||
LMMNOEIH_00840 | 4.8e-136 | 2.7.13.3 | T | Histidine kinase | ||
LMMNOEIH_00841 | 1.2e-13 | 4.1.1.44 | S | Cupin domain | ||
LMMNOEIH_00842 | 6.9e-115 | S | phosphoesterase or phosphohydrolase | |||
LMMNOEIH_00843 | 2e-121 | |||||
LMMNOEIH_00844 | 1.5e-69 | |||||
LMMNOEIH_00845 | 6e-75 | V | Abi-like protein | |||
LMMNOEIH_00846 | 0.0 | hepA | L | SNF2 family N-terminal domain | ||
LMMNOEIH_00847 | 0.0 | V | Type II restriction enzyme, methylase | |||
LMMNOEIH_00848 | 0.0 | L | DEAD-like helicases superfamily | |||
LMMNOEIH_00849 | 0.0 | L | UvrD-like helicase C-terminal domain | |||
LMMNOEIH_00850 | 1.9e-56 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
LMMNOEIH_00851 | 2.2e-11 | V | COG1403 Restriction endonuclease | |||
LMMNOEIH_00853 | 5.6e-15 | |||||
LMMNOEIH_00854 | 5.4e-08 | E | Zn peptidase | |||
LMMNOEIH_00857 | 0.0 | S | Protein of unknown function DUF262 | |||
LMMNOEIH_00858 | 7.4e-23 | S | Protein of unknown function DUF262 | |||
LMMNOEIH_00860 | 3.6e-125 | 3.2.1.8 | S | alpha beta | ||
LMMNOEIH_00861 | 2.3e-84 | 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 | ||
LMMNOEIH_00862 | 3.8e-187 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
LMMNOEIH_00863 | 1.3e-107 | kcsA | U | Ion channel | ||
LMMNOEIH_00864 | 6e-40 | pepC | 3.4.22.40 | E | homocysteine catabolic process | |
LMMNOEIH_00865 | 0.0 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_00866 | 3.9e-108 | 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 | ||
LMMNOEIH_00867 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
LMMNOEIH_00868 | 2.4e-47 | yhbY | J | CRS1_YhbY | ||
LMMNOEIH_00869 | 9.6e-146 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway | |
LMMNOEIH_00870 | 2.2e-201 | S | Glycosyltransferase, group 2 family protein | |||
LMMNOEIH_00871 | 2.7e-140 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
LMMNOEIH_00872 | 8.1e-221 | E | Aminotransferase class I and II | |||
LMMNOEIH_00873 | 1.1e-144 | bioM | P | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_00874 | 1.8e-306 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
LMMNOEIH_00875 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LMMNOEIH_00876 | 0.0 | S | Tetratricopeptide repeat | |||
LMMNOEIH_00877 | 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 | |
LMMNOEIH_00878 | 8.2e-213 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
LMMNOEIH_00879 | 3.8e-84 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LMMNOEIH_00880 | 6.7e-268 | ykoD | P | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_00881 | 3.1e-145 | cbiQ | P | Cobalt transport protein | ||
LMMNOEIH_00882 | 2.3e-251 | argE | E | Peptidase dimerisation domain | ||
LMMNOEIH_00883 | 3.6e-93 | S | Protein of unknown function (DUF3043) | |||
LMMNOEIH_00884 | 5.4e-246 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LMMNOEIH_00885 | 8.6e-142 | S | Domain of unknown function (DUF4191) | |||
LMMNOEIH_00886 | 2.3e-281 | glnA | 6.3.1.2 | E | glutamine synthetase | |
LMMNOEIH_00887 | 4e-42 | V | DNA modification | |||
LMMNOEIH_00888 | 8.3e-113 | ung2 | 3.2.2.27 | L | Uracil DNA glycosylase superfamily | |
LMMNOEIH_00889 | 1.5e-17 | L | HNH endonuclease | |||
LMMNOEIH_00891 | 2.9e-17 | |||||
LMMNOEIH_00892 | 2.5e-95 | yvdD | 3.2.2.10 | S | Possible lysine decarboxylase | |
LMMNOEIH_00894 | 2.9e-154 | 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 | |
LMMNOEIH_00895 | 2.4e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LMMNOEIH_00896 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LMMNOEIH_00897 | 1.1e-95 | |||||
LMMNOEIH_00898 | 1.9e-203 | 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 | |
LMMNOEIH_00899 | 6.7e-215 | 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 | |
LMMNOEIH_00900 | 2.8e-179 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LMMNOEIH_00901 | 3.9e-240 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
LMMNOEIH_00902 | 7.1e-186 | 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 | |
LMMNOEIH_00903 | 1.9e-84 | argR | K | Regulates arginine biosynthesis genes | ||
LMMNOEIH_00904 | 4.6e-238 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LMMNOEIH_00905 | 1.3e-279 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
LMMNOEIH_00906 | 9.7e-94 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LMMNOEIH_00907 | 5.6e-136 | S | Putative ABC-transporter type IV | |||
LMMNOEIH_00908 | 3.9e-133 | S | Protein of unknown function (DUF975) | |||
LMMNOEIH_00909 | 9.8e-173 | S | Protein of unknown function (DUF975) | |||
LMMNOEIH_00910 | 3.8e-251 | 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) | |
LMMNOEIH_00911 | 7.4e-141 | L | Tetratricopeptide repeat | |||
LMMNOEIH_00912 | 1.1e-192 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
LMMNOEIH_00913 | 2.9e-134 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LMMNOEIH_00914 | 3e-116 | trkA | P | TrkA-N domain | ||
LMMNOEIH_00915 | 2.1e-266 | trkB | P | Cation transport protein | ||
LMMNOEIH_00916 | 2.9e-176 | 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 | |
LMMNOEIH_00917 | 5.3e-261 | recN | L | May be involved in recombinational repair of damaged DNA | ||
LMMNOEIH_00918 | 4.4e-123 | S | Haloacid dehalogenase-like hydrolase | |||
LMMNOEIH_00919 | 4.5e-121 | S | ABC-2 family transporter protein | |||
LMMNOEIH_00920 | 2.3e-173 | V | ATPases associated with a variety of cellular activities | |||
LMMNOEIH_00921 | 1.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
LMMNOEIH_00922 | 1.1e-23 | C | Acetamidase/Formamidase family | |||
LMMNOEIH_00923 | 1.6e-44 | L | transposition | |||
LMMNOEIH_00924 | 0.0 | S | Histidine phosphatase superfamily (branch 2) | |||
LMMNOEIH_00925 | 1.7e-94 | S | Pyridoxamine 5'-phosphate oxidase | |||
LMMNOEIH_00926 | 8.8e-23 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_00927 | 6.4e-96 | bcp | 1.11.1.15 | O | Redoxin | |
LMMNOEIH_00929 | 7.4e-77 | 3.4.13.22 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | ||
LMMNOEIH_00930 | 1.5e-161 | S | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |||
LMMNOEIH_00931 | 6.9e-164 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
LMMNOEIH_00932 | 7.7e-145 | |||||
LMMNOEIH_00933 | 7.4e-174 | G | Fic/DOC family | |||
LMMNOEIH_00934 | 4.7e-105 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
LMMNOEIH_00935 | 4.4e-231 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_00936 | 2.3e-284 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
LMMNOEIH_00937 | 1.4e-250 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
LMMNOEIH_00938 | 1.9e-242 | 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 | |
LMMNOEIH_00939 | 3.2e-101 | |||||
LMMNOEIH_00940 | 1.8e-141 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LMMNOEIH_00941 | 1.7e-201 | 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) | |
LMMNOEIH_00943 | 5.4e-121 | |||||
LMMNOEIH_00944 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
LMMNOEIH_00945 | 1.1e-83 | 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 | |
LMMNOEIH_00946 | 1.9e-139 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LMMNOEIH_00947 | 5e-143 | 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 | ||
LMMNOEIH_00949 | 9.8e-135 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LMMNOEIH_00950 | 5.8e-92 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
LMMNOEIH_00951 | 6.1e-177 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
LMMNOEIH_00952 | 1e-223 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LMMNOEIH_00953 | 3e-139 | hisF | 4.1.3.27 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
LMMNOEIH_00954 | 2.9e-72 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
LMMNOEIH_00955 | 2.7e-296 | 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 | |
LMMNOEIH_00956 | 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 | |
LMMNOEIH_00957 | 1e-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 | |
LMMNOEIH_00958 | 1e-179 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
LMMNOEIH_00959 | 4.2e-97 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
LMMNOEIH_00960 | 1.9e-40 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
LMMNOEIH_00961 | 3.9e-156 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
LMMNOEIH_00962 | 1e-102 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LMMNOEIH_00963 | 9.9e-172 | S | Bacterial protein of unknown function (DUF881) | |||
LMMNOEIH_00964 | 4.2e-45 | sbp | S | Protein of unknown function (DUF1290) | ||
LMMNOEIH_00965 | 1.6e-141 | S | Bacterial protein of unknown function (DUF881) | |||
LMMNOEIH_00966 | 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) | |
LMMNOEIH_00967 | 3.5e-112 | pgsA1 | 2.7.8.11, 2.7.8.5 | I | CDP-alcohol phosphatidyltransferase | |
LMMNOEIH_00968 | 5.2e-128 | yebC | K | transcriptional regulatory protein | ||
LMMNOEIH_00969 | 1e-99 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
LMMNOEIH_00970 | 1e-105 | 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 | |
LMMNOEIH_00971 | 1.6e-199 | 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 | |
LMMNOEIH_00972 | 1e-58 | yajC | U | Preprotein translocase subunit | ||
LMMNOEIH_00973 | 1.8e-99 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
LMMNOEIH_00974 | 2.2e-221 | 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 | |
LMMNOEIH_00975 | 2.6e-161 | 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 | |
LMMNOEIH_00976 | 3e-246 | |||||
LMMNOEIH_00977 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LMMNOEIH_00978 | 8.2e-34 | |||||
LMMNOEIH_00979 | 1.5e-161 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LMMNOEIH_00980 | 9.1e-144 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LMMNOEIH_00981 | 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 | |
LMMNOEIH_00982 | 1.1e-69 | |||||
LMMNOEIH_00984 | 1.4e-264 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
LMMNOEIH_00985 | 0.0 | pafB | K | WYL domain | ||
LMMNOEIH_00986 | 2.1e-54 | |||||
LMMNOEIH_00987 | 0.0 | helY | L | DEAD DEAH box helicase | ||
LMMNOEIH_00988 | 3.9e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
LMMNOEIH_00989 | 3e-141 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
LMMNOEIH_00990 | 4.6e-61 | |||||
LMMNOEIH_00991 | 9.7e-112 | K | helix_turn_helix, mercury resistance | |||
LMMNOEIH_00992 | 4.7e-76 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LMMNOEIH_00993 | 5.4e-36 | |||||
LMMNOEIH_00994 | 2.5e-08 | |||||
LMMNOEIH_01001 | 1.6e-156 | S | PAC2 family | |||
LMMNOEIH_01002 | 6.9e-156 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LMMNOEIH_01003 | 5.1e-158 | G | Fructosamine kinase | |||
LMMNOEIH_01004 | 2.4e-188 | 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 | ||
LMMNOEIH_01005 | 1.1e-195 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LMMNOEIH_01006 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
LMMNOEIH_01007 | 4.2e-203 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LMMNOEIH_01008 | 2.2e-41 | nadR | H | ATPase kinase involved in NAD metabolism | ||
LMMNOEIH_01009 | 2.5e-49 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | ATPase kinase involved in NAD metabolism | |
LMMNOEIH_01010 | 5.6e-112 | pnuC | H | Nicotinamide mononucleotide transporter | ||
LMMNOEIH_01011 | 1.2e-08 | pnuC | H | Nicotinamide mononucleotide transporter | ||
LMMNOEIH_01012 | 8e-301 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
LMMNOEIH_01013 | 7.4e-163 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LMMNOEIH_01014 | 2.4e-32 | secG | U | Preprotein translocase SecG subunit | ||
LMMNOEIH_01015 | 2.8e-148 | 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) | |
LMMNOEIH_01016 | 1.9e-220 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
LMMNOEIH_01017 | 1.3e-171 | whiA | K | May be required for sporulation | ||
LMMNOEIH_01018 | 2.3e-170 | rapZ | S | Displays ATPase and GTPase activities | ||
LMMNOEIH_01019 | 7.1e-183 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
LMMNOEIH_01020 | 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 | ||
LMMNOEIH_01021 | 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 | ||
LMMNOEIH_01022 | 9.3e-220 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01023 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01024 | 1.4e-139 | S | Domain of unknown function (DUF4194) | |||
LMMNOEIH_01025 | 1.6e-272 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01026 | 2e-13 | |||||
LMMNOEIH_01028 | 1.1e-65 | ogt | 2.1.1.63 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
LMMNOEIH_01029 | 4.7e-111 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
LMMNOEIH_01030 | 1.2e-299 | ybiT | S | ABC transporter | ||
LMMNOEIH_01031 | 4e-157 | S | IMP dehydrogenase activity | |||
LMMNOEIH_01032 | 3.7e-276 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LMMNOEIH_01033 | 1.3e-145 | mazG | 3.6.1.66 | S | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01034 | 6.8e-146 | |||||
LMMNOEIH_01035 | 1e-98 | |||||
LMMNOEIH_01038 | 1e-182 | cat | P | Cation efflux family | ||
LMMNOEIH_01039 | 3.6e-76 | S | Psort location CytoplasmicMembrane, score | |||
LMMNOEIH_01040 | 1.1e-219 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
LMMNOEIH_01041 | 5.3e-144 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
LMMNOEIH_01042 | 4.6e-199 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
LMMNOEIH_01043 | 6.7e-72 | K | MerR family regulatory protein | |||
LMMNOEIH_01044 | 5.3e-119 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LMMNOEIH_01045 | 4.5e-185 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
LMMNOEIH_01046 | 7.8e-119 | yoaP | E | YoaP-like | ||
LMMNOEIH_01048 | 5.8e-194 | 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 | |
LMMNOEIH_01049 | 7.6e-103 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
LMMNOEIH_01050 | 6.4e-148 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
LMMNOEIH_01051 | 9.2e-94 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
LMMNOEIH_01052 | 6.5e-179 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LMMNOEIH_01053 | 0.0 | comE | S | Competence protein | ||
LMMNOEIH_01054 | 2.2e-92 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
LMMNOEIH_01055 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LMMNOEIH_01056 | 1.5e-142 | ET | Bacterial periplasmic substrate-binding proteins | |||
LMMNOEIH_01057 | 5.7e-172 | corA | P | CorA-like Mg2+ transporter protein | ||
LMMNOEIH_01058 | 1.5e-163 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LMMNOEIH_01059 | 5.2e-65 | 3.4.22.70 | M | Sortase family | ||
LMMNOEIH_01060 | 5.6e-83 | 3.4.22.70 | M | Sortase family | ||
LMMNOEIH_01061 | 4.6e-302 | M | domain protein | |||
LMMNOEIH_01062 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
LMMNOEIH_01063 | 1.3e-232 | XK27_00240 | K | Fic/DOC family | ||
LMMNOEIH_01065 | 6.2e-117 | |||||
LMMNOEIH_01066 | 4.3e-143 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LMMNOEIH_01067 | 3.6e-67 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
LMMNOEIH_01068 | 2.6e-242 | 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 | |
LMMNOEIH_01069 | 9e-72 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
LMMNOEIH_01070 | 6.1e-108 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
LMMNOEIH_01071 | 8.4e-210 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
LMMNOEIH_01072 | 1.2e-230 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
LMMNOEIH_01073 | 1.1e-268 | G | ABC transporter substrate-binding protein | |||
LMMNOEIH_01074 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
LMMNOEIH_01075 | 3.3e-96 | M | Peptidase family M23 | |||
LMMNOEIH_01076 | 1.6e-61 | |||||
LMMNOEIH_01079 | 5e-125 | XK27_06785 | V | ABC transporter | ||
LMMNOEIH_01080 | 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 | |
LMMNOEIH_01081 | 3.5e-109 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LMMNOEIH_01082 | 2.3e-139 | S | SdpI/YhfL protein family | |||
LMMNOEIH_01083 | 1.8e-50 | sdpR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
LMMNOEIH_01084 | 3.3e-120 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
LMMNOEIH_01085 | 8.1e-218 | yxjG_1 | E | Psort location Cytoplasmic, score 8.87 | ||
LMMNOEIH_01086 | 6.1e-69 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
LMMNOEIH_01087 | 8.8e-109 | J | Acetyltransferase (GNAT) domain | |||
LMMNOEIH_01088 | 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 | |
LMMNOEIH_01089 | 2.9e-162 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LMMNOEIH_01090 | 5.5e-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) | |
LMMNOEIH_01091 | 6.6e-179 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
LMMNOEIH_01092 | 9.3e-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 | |
LMMNOEIH_01093 | 7e-178 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
LMMNOEIH_01094 | 5.2e-278 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
LMMNOEIH_01095 | 4.2e-74 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
LMMNOEIH_01096 | 6.7e-187 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LMMNOEIH_01097 | 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 | |
LMMNOEIH_01098 | 6.8e-19 | |||||
LMMNOEIH_01099 | 6.4e-184 | gguB | U | Branched-chain amino acid transport system / permease component | ||
LMMNOEIH_01100 | 3e-271 | araG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
LMMNOEIH_01101 | 5e-186 | G | Periplasmic binding protein domain | |||
LMMNOEIH_01102 | 5e-178 | GK | ROK family | |||
LMMNOEIH_01103 | 7.1e-126 | xylG | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
LMMNOEIH_01104 | 9.5e-29 | |||||
LMMNOEIH_01105 | 2.9e-43 | 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 | |
LMMNOEIH_01106 | 7.3e-155 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
LMMNOEIH_01107 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
LMMNOEIH_01108 | 1.5e-28 | S | Putative phage holin Dp-1 | |||
LMMNOEIH_01109 | 1.9e-199 | M | Glycosyl hydrolases family 25 | |||
LMMNOEIH_01113 | 1.8e-40 | MU | outer membrane autotransporter barrel domain protein | |||
LMMNOEIH_01114 | 3.7e-19 | |||||
LMMNOEIH_01115 | 8.1e-93 | L | DNA integration | |||
LMMNOEIH_01117 | 2.4e-29 | |||||
LMMNOEIH_01118 | 7.1e-139 | |||||
LMMNOEIH_01120 | 9.9e-301 | S | Psort location Cytoplasmic, score | |||
LMMNOEIH_01121 | 1.1e-142 | |||||
LMMNOEIH_01122 | 1.5e-51 | S | phage tail tape measure protein | |||
LMMNOEIH_01123 | 3.6e-55 | |||||
LMMNOEIH_01125 | 6.4e-35 | |||||
LMMNOEIH_01126 | 7.1e-60 | |||||
LMMNOEIH_01127 | 1.1e-66 | rlfA | S | Protein of unknown function (DUF3800) | ||
LMMNOEIH_01128 | 2.9e-24 | |||||
LMMNOEIH_01129 | 5.9e-61 | |||||
LMMNOEIH_01130 | 2.8e-137 | L | Phage integrase family | |||
LMMNOEIH_01132 | 1.3e-210 | ykiI | ||||
LMMNOEIH_01133 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LMMNOEIH_01134 | 1.9e-121 | 3.6.1.13 | L | NUDIX domain | ||
LMMNOEIH_01135 | 3.5e-171 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
LMMNOEIH_01136 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
LMMNOEIH_01137 | 9.4e-101 | pdtaR | T | Response regulator receiver domain protein | ||
LMMNOEIH_01138 | 1.4e-158 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
LMMNOEIH_01139 | 1.6e-102 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
LMMNOEIH_01140 | 9.8e-28 | L | Protein of unknown function (DUF1524) | |||
LMMNOEIH_01141 | 4.2e-21 | K | Cro/C1-type HTH DNA-binding domain | |||
LMMNOEIH_01142 | 1.8e-128 | S | Uncharacterised protein conserved in bacteria (DUF2326) | |||
LMMNOEIH_01143 | 3.8e-16 | |||||
LMMNOEIH_01144 | 1.3e-66 | S | Psort location Cytoplasmic, score | |||
LMMNOEIH_01146 | 2.3e-17 | K | Psort location Cytoplasmic, score | |||
LMMNOEIH_01148 | 2.8e-146 | 2.7.7.7 | L | Transposase, Mutator family | ||
LMMNOEIH_01149 | 5.3e-152 | L | Phage integrase family | |||
LMMNOEIH_01150 | 3.9e-16 | |||||
LMMNOEIH_01151 | 3.4e-43 | K | Helix-turn-helix domain protein | |||
LMMNOEIH_01152 | 2.7e-13 | K | Helix-turn-helix domain protein | |||
LMMNOEIH_01153 | 6.8e-36 | rplV | S | ASCH | ||
LMMNOEIH_01154 | 9.7e-33 | topB | 5.99.1.2 | L | DNA topoisomerase | |
LMMNOEIH_01155 | 3.2e-118 | L | Integrase core domain | |||
LMMNOEIH_01156 | 2.9e-42 | L | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01157 | 2.6e-111 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
LMMNOEIH_01159 | 1.3e-64 | dam2 | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
LMMNOEIH_01160 | 5e-68 | |||||
LMMNOEIH_01161 | 8.5e-24 | |||||
LMMNOEIH_01162 | 1.1e-97 | |||||
LMMNOEIH_01163 | 1.5e-45 | S | PrgI family protein | |||
LMMNOEIH_01164 | 0.0 | trsE | U | type IV secretory pathway VirB4 | ||
LMMNOEIH_01165 | 1.9e-21 | |||||
LMMNOEIH_01166 | 6.1e-20 | |||||
LMMNOEIH_01168 | 3.4e-08 | D | AAA domain | |||
LMMNOEIH_01169 | 5.5e-56 | D | AAA domain | |||
LMMNOEIH_01171 | 6.9e-36 | S | Transcription factor WhiB | |||
LMMNOEIH_01172 | 9.6e-87 | S | Helix-turn-helix domain | |||
LMMNOEIH_01173 | 1.8e-19 | S | Helix-turn-helix domain | |||
LMMNOEIH_01174 | 4.5e-10 | |||||
LMMNOEIH_01175 | 2e-28 | |||||
LMMNOEIH_01176 | 6.3e-105 | |||||
LMMNOEIH_01180 | 2.5e-305 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
LMMNOEIH_01181 | 8.8e-176 | terC | P | Integral membrane protein, TerC family | ||
LMMNOEIH_01182 | 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 | ||
LMMNOEIH_01183 | 9.1e-116 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
LMMNOEIH_01184 | 8.3e-255 | rpsA | J | Ribosomal protein S1 | ||
LMMNOEIH_01185 | 1.6e-160 | 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 | |
LMMNOEIH_01186 | 2.9e-172 | P | Zinc-uptake complex component A periplasmic | |||
LMMNOEIH_01187 | 2e-160 | znuC | P | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_01188 | 1e-140 | znuB | U | ABC 3 transport family | ||
LMMNOEIH_01189 | 7.8e-88 | 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) | |
LMMNOEIH_01190 | 3e-102 | carD | K | CarD-like/TRCF domain | ||
LMMNOEIH_01191 | 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 |
LMMNOEIH_01192 | 7.8e-129 | T | Response regulator receiver domain protein | |||
LMMNOEIH_01193 | 6.8e-188 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LMMNOEIH_01194 | 1e-139 | ctsW | S | Phosphoribosyl transferase domain | ||
LMMNOEIH_01195 | 1.1e-152 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
LMMNOEIH_01196 | 1.5e-71 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
LMMNOEIH_01197 | 4.8e-213 | |||||
LMMNOEIH_01198 | 0.0 | S | Glycosyl transferase, family 2 | |||
LMMNOEIH_01199 | 3.4e-54 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
LMMNOEIH_01200 | 4.8e-199 | K | Cell envelope-related transcriptional attenuator domain | |||
LMMNOEIH_01202 | 9e-170 | K | Cell envelope-related transcriptional attenuator domain | |||
LMMNOEIH_01203 | 0.0 | D | FtsK/SpoIIIE family | |||
LMMNOEIH_01204 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
LMMNOEIH_01205 | 6e-277 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
LMMNOEIH_01206 | 5e-138 | yplQ | S | Haemolysin-III related | ||
LMMNOEIH_01207 | 2.6e-80 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
LMMNOEIH_01208 | 1.2e-73 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
LMMNOEIH_01209 | 9.4e-283 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
LMMNOEIH_01210 | 3e-91 | |||||
LMMNOEIH_01212 | 4.4e-183 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LMMNOEIH_01213 | 2e-103 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
LMMNOEIH_01214 | 2e-71 | divIC | D | Septum formation initiator | ||
LMMNOEIH_01215 | 1.5e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
LMMNOEIH_01216 | 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 | ||
LMMNOEIH_01217 | 1.7e-113 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
LMMNOEIH_01218 | 3.6e-99 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
LMMNOEIH_01219 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
LMMNOEIH_01220 | 9.6e-180 | ybbD | 3.2.1.52 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
LMMNOEIH_01221 | 6.2e-40 | ybdD | S | Selenoprotein, putative | ||
LMMNOEIH_01222 | 0.0 | cstA | T | 5TM C-terminal transporter carbon starvation CstA | ||
LMMNOEIH_01223 | 1.3e-51 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
LMMNOEIH_01224 | 6.7e-142 | azlC | E | AzlC protein | ||
LMMNOEIH_01225 | 1.3e-87 | M | Protein of unknown function (DUF3737) | |||
LMMNOEIH_01226 | 1.1e-80 | 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 | ||
LMMNOEIH_01227 | 2.2e-145 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LMMNOEIH_01228 | 2.1e-174 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LMMNOEIH_01229 | 7.1e-305 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LMMNOEIH_01230 | 1.7e-215 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LMMNOEIH_01231 | 3.4e-146 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
LMMNOEIH_01232 | 3.4e-277 | 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 | |
LMMNOEIH_01233 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
LMMNOEIH_01234 | 2.3e-238 | S | Putative esterase | |||
LMMNOEIH_01235 | 1.9e-142 | ybbL | V | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_01236 | 1.8e-134 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
LMMNOEIH_01237 | 2e-270 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
LMMNOEIH_01238 | 1.2e-126 | S | Enoyl-(Acyl carrier protein) reductase | |||
LMMNOEIH_01239 | 2.4e-234 | rutG | F | Permease family | ||
LMMNOEIH_01240 | 5.4e-155 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LMMNOEIH_01241 | 7e-141 | K | helix_turn_helix, arabinose operon control protein | |||
LMMNOEIH_01242 | 4e-137 | S | Sulfite exporter TauE/SafE | |||
LMMNOEIH_01243 | 3.3e-93 | S | ECF transporter, substrate-specific component | |||
LMMNOEIH_01244 | 1.4e-112 | 2.7.1.48 | F | uridine kinase | ||
LMMNOEIH_01245 | 2.5e-172 | korD | 1.2.7.3 | C | Domain of unknown function (DUF362) | |
LMMNOEIH_01246 | 8.7e-224 | C | Na H antiporter family protein | |||
LMMNOEIH_01247 | 1.8e-176 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
LMMNOEIH_01248 | 7e-118 | |||||
LMMNOEIH_01249 | 3.7e-16 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
LMMNOEIH_01250 | 3.3e-55 | KLT | Protein tyrosine kinase | |||
LMMNOEIH_01251 | 8.1e-258 | EGP | Transmembrane secretion effector | |||
LMMNOEIH_01252 | 0.0 | cysB | 4.2.1.22 | EGP | Major facilitator Superfamily | |
LMMNOEIH_01253 | 2.2e-11 | |||||
LMMNOEIH_01254 | 8e-58 | yccF | S | Inner membrane component domain | ||
LMMNOEIH_01255 | 1.2e-118 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_01256 | 3e-213 | G | Transmembrane secretion effector | |||
LMMNOEIH_01257 | 1.6e-16 | K | addiction module antidote protein HigA | |||
LMMNOEIH_01258 | 2.5e-239 | S | HipA-like C-terminal domain | |||
LMMNOEIH_01259 | 3.9e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LMMNOEIH_01260 | 2e-141 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LMMNOEIH_01261 | 1.6e-265 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
LMMNOEIH_01262 | 0.0 | tcsS2 | T | Histidine kinase | ||
LMMNOEIH_01263 | 1.9e-130 | K | helix_turn_helix, Lux Regulon | |||
LMMNOEIH_01264 | 0.0 | MV | MacB-like periplasmic core domain | |||
LMMNOEIH_01265 | 5.1e-142 | V | ABC transporter, ATP-binding protein | |||
LMMNOEIH_01266 | 8.2e-193 | K | helix_turn_helix ASNC type | |||
LMMNOEIH_01267 | 6.9e-150 | P | Cobalt transport protein | |||
LMMNOEIH_01268 | 4.7e-304 | 3.6.3.24 | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
LMMNOEIH_01269 | 4.3e-95 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
LMMNOEIH_01270 | 8.5e-251 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
LMMNOEIH_01271 | 2e-163 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
LMMNOEIH_01272 | 4e-83 | yraN | L | Belongs to the UPF0102 family | ||
LMMNOEIH_01273 | 1.8e-292 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
LMMNOEIH_01274 | 2.9e-254 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
LMMNOEIH_01275 | 0.0 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
LMMNOEIH_01276 | 5.7e-177 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
LMMNOEIH_01277 | 4.8e-117 | safC | S | O-methyltransferase | ||
LMMNOEIH_01278 | 3.9e-246 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
LMMNOEIH_01281 | 1.6e-236 | 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 | ||
LMMNOEIH_01282 | 7.3e-124 | 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 | |
LMMNOEIH_01283 | 2.3e-113 | 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 | |
LMMNOEIH_01284 | 0.0 | E | ABC transporter, substrate-binding protein, family 5 | |||
LMMNOEIH_01285 | 5.3e-252 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01286 | 1.2e-172 | yjfF | U | Branched-chain amino acid transport system / permease component | ||
LMMNOEIH_01287 | 3.4e-181 | ytfT | U | Branched-chain amino acid transport system / permease component | ||
LMMNOEIH_01288 | 6e-288 | ytfR | 3.6.3.17 | G | ATPases associated with a variety of cellular activities | |
LMMNOEIH_01289 | 2.4e-165 | G | Periplasmic binding protein domain | |||
LMMNOEIH_01290 | 0.0 | lpqB | S | Lipoprotein LpqB beta-propeller domain | ||
LMMNOEIH_01291 | 4.4e-286 | mtrB | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |
LMMNOEIH_01292 | 2.4e-133 | KT | Transcriptional regulatory protein, C terminal | |||
LMMNOEIH_01293 | 3.2e-248 | rarA | L | Recombination factor protein RarA | ||
LMMNOEIH_01294 | 0.0 | L | DEAD DEAH box helicase | |||
LMMNOEIH_01295 | 2.4e-189 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
LMMNOEIH_01296 | 1.7e-199 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_01297 | 1.8e-111 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_01298 | 2e-152 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LMMNOEIH_01299 | 6.2e-137 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
LMMNOEIH_01300 | 6.7e-139 | glnQ | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
LMMNOEIH_01301 | 4.6e-280 | glnP | E | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_01302 | 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) | |
LMMNOEIH_01303 | 5.3e-251 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
LMMNOEIH_01304 | 1.5e-216 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
LMMNOEIH_01305 | 1.6e-140 | 3.5.2.10 | S | Creatinine amidohydrolase | ||
LMMNOEIH_01306 | 1.6e-244 | proP | EGP | Sugar (and other) transporter | ||
LMMNOEIH_01307 | 7e-248 | purR | QT | Purine catabolism regulatory protein-like family | ||
LMMNOEIH_01308 | 2.6e-28 | purR | QT | Purine catabolism regulatory protein-like family | ||
LMMNOEIH_01309 | 3.7e-254 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
LMMNOEIH_01310 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
LMMNOEIH_01311 | 4.6e-188 | uspA | T | Belongs to the universal stress protein A family | ||
LMMNOEIH_01312 | 1.2e-182 | S | Protein of unknown function (DUF3027) | |||
LMMNOEIH_01313 | 4.5e-67 | cspB | K | 'Cold-shock' DNA-binding domain | ||
LMMNOEIH_01314 | 0.0 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
LMMNOEIH_01315 | 2.6e-132 | KT | Response regulator receiver domain protein | |||
LMMNOEIH_01316 | 1.3e-124 | |||||
LMMNOEIH_01318 | 8.7e-290 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
LMMNOEIH_01319 | 8.5e-77 | S | LytR cell envelope-related transcriptional attenuator | |||
LMMNOEIH_01320 | 4.4e-137 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
LMMNOEIH_01321 | 4e-182 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
LMMNOEIH_01322 | 1.2e-174 | S | Protein of unknown function DUF58 | |||
LMMNOEIH_01323 | 8.8e-90 | |||||
LMMNOEIH_01324 | 1.6e-191 | S | von Willebrand factor (vWF) type A domain | |||
LMMNOEIH_01325 | 5e-182 | S | von Willebrand factor (vWF) type A domain | |||
LMMNOEIH_01326 | 3.2e-61 | |||||
LMMNOEIH_01327 | 6e-277 | S | PGAP1-like protein | |||
LMMNOEIH_01328 | 1.6e-279 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
LMMNOEIH_01329 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
LMMNOEIH_01330 | 1.4e-41 | hup | L | Belongs to the bacterial histone-like protein family | ||
LMMNOEIH_01331 | 1.8e-57 | |||||
LMMNOEIH_01332 | 3.7e-140 | C | FMN binding | |||
LMMNOEIH_01333 | 1.3e-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 | |
LMMNOEIH_01334 | 1.4e-24 | pup | S | Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation | ||
LMMNOEIH_01335 | 3.3e-160 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
LMMNOEIH_01336 | 4.4e-302 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
LMMNOEIH_01337 | 6.4e-282 | arc | O | AAA ATPase forming ring-shaped complexes | ||
LMMNOEIH_01338 | 1.6e-123 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
LMMNOEIH_01339 | 1.1e-178 | 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 | |
LMMNOEIH_01340 | 2.7e-134 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LMMNOEIH_01341 | 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 | ||
LMMNOEIH_01342 | 1.6e-227 | 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 | |
LMMNOEIH_01343 | 1.4e-46 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
LMMNOEIH_01344 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
LMMNOEIH_01346 | 1.2e-106 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LMMNOEIH_01347 | 3.7e-171 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LMMNOEIH_01348 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
LMMNOEIH_01349 | 1.1e-239 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
LMMNOEIH_01350 | 1.8e-75 | 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 | ||
LMMNOEIH_01351 | 2e-103 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
LMMNOEIH_01352 | 9.5e-233 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LMMNOEIH_01353 | 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 | ||
LMMNOEIH_01354 | 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 | ||
LMMNOEIH_01355 | 1.2e-61 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
LMMNOEIH_01356 | 4e-187 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
LMMNOEIH_01358 | 1.5e-197 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
LMMNOEIH_01359 | 6.5e-226 | M | Glycosyl transferase 4-like domain | |||
LMMNOEIH_01360 | 4.8e-227 | 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 | |
LMMNOEIH_01361 | 4.3e-138 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
LMMNOEIH_01362 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
LMMNOEIH_01363 | 4.3e-33 | |||||
LMMNOEIH_01364 | 5.5e-308 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
LMMNOEIH_01365 | 1.4e-284 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LMMNOEIH_01366 | 8.3e-185 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
LMMNOEIH_01367 | 9.7e-236 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
LMMNOEIH_01368 | 2.1e-247 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01369 | 1.1e-183 | rihB | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LMMNOEIH_01370 | 5.6e-214 | 1.1.1.1 | C | Iron-containing alcohol dehydrogenase | ||
LMMNOEIH_01371 | 7.4e-129 | trpF | 5.3.1.24 | E | N-(5'phosphoribosyl)anthranilate (PRA) isomerase | |
LMMNOEIH_01372 | 9.1e-189 | yeiI | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
LMMNOEIH_01373 | 7.2e-203 | psuK | 2.7.1.15, 2.7.1.45, 2.7.1.83 | G | pfkB family carbohydrate kinase | |
LMMNOEIH_01374 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LMMNOEIH_01375 | 8.8e-89 | zur | P | Belongs to the Fur family | ||
LMMNOEIH_01376 | 1.3e-226 | 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) | |
LMMNOEIH_01377 | 1.1e-84 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
LMMNOEIH_01378 | 1.3e-182 | adh3 | C | Zinc-binding dehydrogenase | ||
LMMNOEIH_01379 | 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) | |
LMMNOEIH_01380 | 9.8e-256 | macB_8 | V | MacB-like periplasmic core domain | ||
LMMNOEIH_01381 | 4.4e-147 | M | Conserved repeat domain | |||
LMMNOEIH_01382 | 2.8e-134 | V | ATPases associated with a variety of cellular activities | |||
LMMNOEIH_01383 | 9.1e-73 | |||||
LMMNOEIH_01384 | 7.6e-14 | S | Domain of unknown function (DUF4143) | |||
LMMNOEIH_01385 | 3.1e-127 | XK27_08050 | O | prohibitin homologues | ||
LMMNOEIH_01386 | 1.4e-43 | XAC3035 | O | Glutaredoxin | ||
LMMNOEIH_01387 | 1.2e-74 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LMMNOEIH_01388 | 1.1e-222 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
LMMNOEIH_01389 | 4.9e-98 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
LMMNOEIH_01390 | 6.5e-193 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LMMNOEIH_01391 | 7.6e-155 | metQ | M | NLPA lipoprotein | ||
LMMNOEIH_01392 | 5.3e-200 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
LMMNOEIH_01393 | 9e-143 | cjaA | ET | Bacterial periplasmic substrate-binding proteins | ||
LMMNOEIH_01394 | 6.5e-151 | glnQ | 3.6.3.21 | E | ATP binding protein of ABC transporter for glutamate aspartate K02028 | |
LMMNOEIH_01395 | 3.6e-120 | E | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01396 | 3.1e-108 | papP | E | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_01397 | 1e-113 | K | acetyltransferase | |||
LMMNOEIH_01401 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
LMMNOEIH_01403 | 7.5e-175 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
LMMNOEIH_01405 | 2e-214 | ybiR | P | Citrate transporter | ||
LMMNOEIH_01406 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LMMNOEIH_01407 | 9.9e-288 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LMMNOEIH_01408 | 3.1e-270 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
LMMNOEIH_01409 | 2.7e-102 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
LMMNOEIH_01410 | 3.9e-92 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
LMMNOEIH_01411 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LMMNOEIH_01412 | 0.0 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_01413 | 3.8e-218 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LMMNOEIH_01414 | 1.5e-191 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
LMMNOEIH_01415 | 4e-139 | sapF | E | ATPases associated with a variety of cellular activities | ||
LMMNOEIH_01416 | 1.4e-136 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
LMMNOEIH_01417 | 1.2e-139 | EP | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01418 | 1.3e-166 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01419 | 2.5e-292 | E | ABC transporter, substrate-binding protein, family 5 | |||
LMMNOEIH_01420 | 7e-242 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
LMMNOEIH_01421 | 5.9e-143 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
LMMNOEIH_01422 | 1.8e-275 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01423 | 2.2e-243 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01424 | 2.2e-311 | abfA1 | 3.2.1.55 | GH51 | G | arabinose metabolic process |
LMMNOEIH_01425 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01426 | 4.5e-239 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01427 | 3.3e-127 | 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 | |
LMMNOEIH_01428 | 4e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
LMMNOEIH_01429 | 0.0 | cydD | V | ABC transporter transmembrane region | ||
LMMNOEIH_01430 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LMMNOEIH_01431 | 1.8e-297 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
LMMNOEIH_01432 | 1e-130 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
LMMNOEIH_01433 | 0.0 | araB | 2.7.1.16, 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LMMNOEIH_01434 | 3.1e-209 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_01435 | 2e-285 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
LMMNOEIH_01436 | 1.2e-188 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
LMMNOEIH_01437 | 1.6e-241 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
LMMNOEIH_01438 | 1.2e-291 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LMMNOEIH_01439 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
LMMNOEIH_01440 | 2.2e-271 | mmuP | E | amino acid | ||
LMMNOEIH_01441 | 2.8e-64 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
LMMNOEIH_01443 | 5.2e-121 | cyaA | 4.6.1.1 | S | CYTH | |
LMMNOEIH_01444 | 9.3e-170 | trxA2 | O | Tetratricopeptide repeat | ||
LMMNOEIH_01445 | 2.7e-180 | |||||
LMMNOEIH_01446 | 5.3e-194 | |||||
LMMNOEIH_01447 | 3.4e-148 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
LMMNOEIH_01448 | 2.3e-122 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
LMMNOEIH_01449 | 2.3e-44 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
LMMNOEIH_01450 | 5.6e-283 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
LMMNOEIH_01451 | 3.6e-163 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
LMMNOEIH_01452 | 3.8e-309 | 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 | |
LMMNOEIH_01453 | 4.5e-149 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
LMMNOEIH_01454 | 4.4e-57 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
LMMNOEIH_01455 | 8.9e-31 | 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 | ||
LMMNOEIH_01456 | 2e-146 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
LMMNOEIH_01457 | 4.5e-207 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
LMMNOEIH_01459 | 7.6e-32 | K | BetR domain | |||
LMMNOEIH_01462 | 4.5e-41 | |||||
LMMNOEIH_01464 | 1.2e-57 | |||||
LMMNOEIH_01466 | 1.3e-139 | L | HNH endonuclease | |||
LMMNOEIH_01468 | 1.2e-277 | S | Terminase | |||
LMMNOEIH_01469 | 3.1e-209 | S | Phage portal protein | |||
LMMNOEIH_01470 | 2.6e-286 | S | Caudovirus prohead serine protease | |||
LMMNOEIH_01471 | 7.4e-55 | |||||
LMMNOEIH_01472 | 1.6e-61 | |||||
LMMNOEIH_01473 | 6e-65 | |||||
LMMNOEIH_01474 | 2.1e-61 | |||||
LMMNOEIH_01475 | 3.1e-43 | |||||
LMMNOEIH_01476 | 0.0 | NT | phage tail tape measure protein | |||
LMMNOEIH_01477 | 1.5e-238 | |||||
LMMNOEIH_01478 | 7.1e-31 | |||||
LMMNOEIH_01480 | 1.4e-21 | |||||
LMMNOEIH_01481 | 6.6e-74 | 3.2.1.20, 3.5.1.28 | GH31 | V | N-acetylmuramoyl-L-alanine amidase | |
LMMNOEIH_01482 | 1.1e-11 | xhlB | S | SPP1 phage holin | ||
LMMNOEIH_01483 | 8.8e-161 | L | Phage integrase family | |||
LMMNOEIH_01484 | 5e-273 | frc | 2.8.3.16 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
LMMNOEIH_01485 | 5.7e-192 | yfdV | S | Membrane transport protein | ||
LMMNOEIH_01486 | 0.0 | oxc | 4.1.1.8 | EH | Thiamine pyrophosphate enzyme, central domain | |
LMMNOEIH_01487 | 2.1e-174 | M | LPXTG-motif cell wall anchor domain protein | |||
LMMNOEIH_01488 | 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 |
LMMNOEIH_01489 | 3.4e-91 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
LMMNOEIH_01490 | 9.4e-98 | mntP | P | Probably functions as a manganese efflux pump | ||
LMMNOEIH_01491 | 6.4e-134 | |||||
LMMNOEIH_01492 | 8.4e-134 | KT | Transcriptional regulatory protein, C terminal | |||
LMMNOEIH_01493 | 3.2e-123 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
LMMNOEIH_01494 | 3.5e-288 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LMMNOEIH_01495 | 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 | |
LMMNOEIH_01496 | 0.0 | S | domain protein | |||
LMMNOEIH_01497 | 1.8e-69 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
LMMNOEIH_01498 | 8.2e-79 | K | helix_turn_helix ASNC type | |||
LMMNOEIH_01499 | 6.6e-245 | 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 | ||
LMMNOEIH_01500 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
LMMNOEIH_01501 | 2.1e-51 | S | Protein of unknown function (DUF2469) | |||
LMMNOEIH_01502 | 2e-205 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
LMMNOEIH_01503 | 6.6e-284 | 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) | |
LMMNOEIH_01504 | 8.6e-287 | 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) | |
LMMNOEIH_01505 | 1.3e-46 | 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) | |
LMMNOEIH_01506 | 6.2e-134 | K | Psort location Cytoplasmic, score | |||
LMMNOEIH_01507 | 6.9e-133 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
LMMNOEIH_01508 | 9.1e-105 | 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) | |
LMMNOEIH_01509 | 3.7e-169 | rmuC | S | RmuC family | ||
LMMNOEIH_01510 | 7.5e-134 | 3.6.3.3, 3.6.3.5, 3.6.3.54 | P | Heavy metal translocating P-type atpase | ||
LMMNOEIH_01511 | 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 | ||
LMMNOEIH_01512 | 2.6e-163 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
LMMNOEIH_01513 | 1.1e-147 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
LMMNOEIH_01514 | 8e-79 | |||||
LMMNOEIH_01515 | 2.8e-210 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LMMNOEIH_01516 | 1.8e-38 | M | Protein of unknown function (DUF3152) | |||
LMMNOEIH_01517 | 1.4e-125 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LMMNOEIH_01519 | 1.7e-70 | rplI | J | Binds to the 23S rRNA | ||
LMMNOEIH_01520 | 3.5e-36 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
LMMNOEIH_01521 | 9.7e-70 | ssb1 | L | Single-stranded DNA-binding protein | ||
LMMNOEIH_01522 | 2.5e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LMMNOEIH_01523 | 3.3e-186 | 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) | |
LMMNOEIH_01524 | 1.3e-174 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
LMMNOEIH_01525 | 1.1e-259 | EGP | Major Facilitator Superfamily | |||
LMMNOEIH_01526 | 3.3e-167 | iunH2 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LMMNOEIH_01527 | 9.7e-197 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_01528 | 1.2e-61 | |||||
LMMNOEIH_01529 | 4.2e-200 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LMMNOEIH_01530 | 3.5e-255 | S | Domain of unknown function (DUF4143) | |||
LMMNOEIH_01531 | 1.4e-305 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LMMNOEIH_01532 | 9.9e-114 | M | Glycosyltransferase like family 2 | |||
LMMNOEIH_01533 | 1.2e-76 | rfbN | GT2 | M | Glycosyl transferase family 2 | |
LMMNOEIH_01534 | 3.1e-109 | wbbX | GT2,GT4 | M | transferase activity, transferring glycosyl groups | |
LMMNOEIH_01535 | 2.3e-24 | rgpF | GT2,GT4 | M | Rhamnan synthesis protein F | |
LMMNOEIH_01536 | 1.4e-110 | rgpC | U | Transport permease protein | ||
LMMNOEIH_01537 | 7e-170 | rgpD | 3.6.3.38 | GM | ABC transporter, ATP-binding protein | |
LMMNOEIH_01538 | 5.5e-31 | licD2 | M | LicD family | ||
LMMNOEIH_01539 | 3.6e-155 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LMMNOEIH_01540 | 4.1e-262 | 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 | |
LMMNOEIH_01541 | 7.7e-199 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LMMNOEIH_01542 | 1.6e-80 | S | enterobacterial common antigen metabolic process | |||
LMMNOEIH_01543 | 6e-36 | |||||
LMMNOEIH_01544 | 1.7e-237 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
LMMNOEIH_01545 | 4.4e-202 | lytC | 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
LMMNOEIH_01546 | 5.8e-258 | S | AAA domain | |||
LMMNOEIH_01547 | 2.3e-68 | |||||
LMMNOEIH_01548 | 1e-10 | |||||
LMMNOEIH_01549 | 2.6e-300 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
LMMNOEIH_01550 | 5.6e-59 | |||||
LMMNOEIH_01552 | 6e-92 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01553 | 1.2e-46 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01554 | 7e-30 | yuxJ | EGP | Major facilitator Superfamily | ||
LMMNOEIH_01555 | 4e-287 | recE | 2.7.7.7, 3.6.4.12 | L | Psort location Cytoplasmic, score | |
LMMNOEIH_01556 | 9.5e-110 | 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 | |
LMMNOEIH_01557 | 2.3e-254 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LMMNOEIH_01558 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
LMMNOEIH_01559 | 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 | ||
LMMNOEIH_01560 | 2.4e-153 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LMMNOEIH_01561 | 0.0 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
LMMNOEIH_01562 | 1.1e-38 | csoR | S | Metal-sensitive transcriptional repressor | ||
LMMNOEIH_01563 | 1.4e-133 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LMMNOEIH_01564 | 6.6e-246 | G | Major Facilitator Superfamily | |||
LMMNOEIH_01565 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
LMMNOEIH_01566 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
LMMNOEIH_01567 | 1.5e-264 | KLT | Protein tyrosine kinase | |||
LMMNOEIH_01568 | 0.0 | S | Fibronectin type 3 domain | |||
LMMNOEIH_01569 | 1.3e-225 | S | ATPase family associated with various cellular activities (AAA) | |||
LMMNOEIH_01570 | 8.3e-221 | S | Protein of unknown function DUF58 | |||
LMMNOEIH_01571 | 0.0 | E | Transglutaminase-like superfamily | |||
LMMNOEIH_01572 | 9.9e-163 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
LMMNOEIH_01573 | 1.3e-104 | B | Belongs to the OprB family | |||
LMMNOEIH_01574 | 1.1e-101 | T | Forkhead associated domain | |||
LMMNOEIH_01575 | 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 | |
LMMNOEIH_01576 | 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 | |
LMMNOEIH_01577 | 6.8e-100 | |||||
LMMNOEIH_01578 | 3.5e-182 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
LMMNOEIH_01579 | 3.3e-126 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LMMNOEIH_01580 | 2.1e-252 | S | UPF0210 protein | |||
LMMNOEIH_01581 | 7.1e-43 | gcvR | T | Belongs to the UPF0237 family | ||
LMMNOEIH_01582 | 1.1e-23 | lmrB | EGP | Major facilitator Superfamily | ||
LMMNOEIH_01583 | 1.5e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
LMMNOEIH_01584 | 1.8e-250 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
LMMNOEIH_01585 | 3.4e-141 | glpR | K | DeoR C terminal sensor domain | ||
LMMNOEIH_01586 | 2e-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 | |
LMMNOEIH_01587 | 1.4e-220 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
LMMNOEIH_01588 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LMMNOEIH_01589 | 2.3e-133 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
LMMNOEIH_01590 | 9.1e-217 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
LMMNOEIH_01591 | 2.3e-80 | J | TM2 domain | |||
LMMNOEIH_01592 | 8.4e-193 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
LMMNOEIH_01593 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
LMMNOEIH_01594 | 1.5e-236 | S | Uncharacterized conserved protein (DUF2183) | |||
LMMNOEIH_01595 | 2.7e-70 | 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 | ||
LMMNOEIH_01596 | 2.1e-207 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
LMMNOEIH_01597 | 3.8e-159 | mhpC | I | Alpha/beta hydrolase family | ||
LMMNOEIH_01598 | 1.7e-113 | F | Domain of unknown function (DUF4916) | |||
LMMNOEIH_01599 | 6e-61 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
LMMNOEIH_01600 | 1.6e-169 | S | G5 | |||
LMMNOEIH_01601 | 2.1e-88 | |||||
LMMNOEIH_01603 | 3.3e-237 | rfbP | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
LMMNOEIH_01604 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
LMMNOEIH_01605 | 2.5e-147 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01606 | 1.4e-161 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01607 | 2.5e-269 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01608 | 1.4e-184 | K | Psort location Cytoplasmic, score | |||
LMMNOEIH_01609 | 2.6e-183 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_01610 | 1.4e-78 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01611 | 7e-136 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01612 | 1.4e-162 | G | PFAM binding-protein-dependent transport systems inner membrane component | |||
LMMNOEIH_01613 | 6.6e-145 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01614 | 0.0 | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
LMMNOEIH_01615 | 9.8e-56 | yccF | S | Inner membrane component domain | ||
LMMNOEIH_01616 | 1.3e-07 | S | Bacteriophage abortive infection AbiH | |||
LMMNOEIH_01617 | 3.1e-44 | S | Domain of unknown function (DUF4143) | |||
LMMNOEIH_01618 | 9.3e-39 | pin | L | Resolvase, N terminal domain | ||
LMMNOEIH_01619 | 1.8e-126 | L | Integrase core domain | |||
LMMNOEIH_01620 | 2.9e-42 | L | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01621 | 1.9e-53 | amyE | 3.2.1.1, 3.2.1.80 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LMMNOEIH_01622 | 3.4e-178 | menD | 2.2.1.9 | H | Thiamine pyrophosphate enzyme, N-terminal TPP binding domain | |
LMMNOEIH_01623 | 1.6e-47 | M | Glycosyltransferase like family 2 | |||
LMMNOEIH_01624 | 3.9e-119 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LMMNOEIH_01625 | 3.1e-63 | C | Polysaccharide pyruvyl transferase | |||
LMMNOEIH_01626 | 6.8e-08 | |||||
LMMNOEIH_01627 | 3e-52 | GT4 | M | Psort location Cytoplasmic, score 8.87 | ||
LMMNOEIH_01628 | 7.5e-139 | M | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01629 | 1.2e-45 | L | Integrase core domain | |||
LMMNOEIH_01630 | 2.6e-177 | L | Integrase core domain | |||
LMMNOEIH_01631 | 4e-185 | L | Transposase and inactivated derivatives IS30 family | |||
LMMNOEIH_01632 | 7.9e-114 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LMMNOEIH_01633 | 3.5e-106 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
LMMNOEIH_01634 | 1.9e-147 | L | Transposase and inactivated derivatives IS30 family | |||
LMMNOEIH_01635 | 2.9e-49 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
LMMNOEIH_01637 | 9.5e-106 | |||||
LMMNOEIH_01638 | 2.8e-14 | |||||
LMMNOEIH_01639 | 3.8e-191 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
LMMNOEIH_01640 | 9.3e-224 | pflA | S | Protein of unknown function (DUF4012) | ||
LMMNOEIH_01641 | 1.7e-84 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
LMMNOEIH_01642 | 1.6e-140 | S | Endonuclease/Exonuclease/phosphatase family | |||
LMMNOEIH_01643 | 2.5e-47 | |||||
LMMNOEIH_01644 | 8.1e-285 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01645 | 2.3e-52 | S | phage tail tape measure protein | |||
LMMNOEIH_01646 | 4.3e-115 | |||||
LMMNOEIH_01647 | 6.9e-115 | S | Psort location Cytoplasmic, score | |||
LMMNOEIH_01649 | 4.4e-07 | S | Psort location Cytoplasmic, score | |||
LMMNOEIH_01651 | 7.2e-70 | |||||
LMMNOEIH_01652 | 5.2e-19 | |||||
LMMNOEIH_01653 | 1.9e-15 | |||||
LMMNOEIH_01654 | 2.1e-149 | L | DNA integration | |||
LMMNOEIH_01655 | 1.5e-17 | |||||
LMMNOEIH_01656 | 9.2e-194 | M | Glycosyl hydrolases family 25 | |||
LMMNOEIH_01657 | 2e-28 | S | Putative phage holin Dp-1 | |||
LMMNOEIH_01658 | 2.8e-249 | 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 | |
LMMNOEIH_01659 | 8.1e-66 | yvbK | 3.1.3.25 | K | Acetyltransferase (GNAT) domain | |
LMMNOEIH_01660 | 8.7e-303 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
LMMNOEIH_01661 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
LMMNOEIH_01662 | 6e-302 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LMMNOEIH_01663 | 1.7e-232 | 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 | |
LMMNOEIH_01664 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
LMMNOEIH_01665 | 2.1e-244 | pbuX | F | Permease family | ||
LMMNOEIH_01666 | 1.5e-106 | 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 | |
LMMNOEIH_01667 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
LMMNOEIH_01668 | 1.7e-61 | S | Domain of unknown function (DUF4418) | |||
LMMNOEIH_01669 | 4.8e-216 | V | FtsX-like permease family | |||
LMMNOEIH_01670 | 1.9e-150 | lolD | V | ABC transporter | ||
LMMNOEIH_01671 | 3.1e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
LMMNOEIH_01672 | 4.5e-51 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
LMMNOEIH_01673 | 5.6e-129 | pgm3 | G | Phosphoglycerate mutase family | ||
LMMNOEIH_01674 | 3.4e-59 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
LMMNOEIH_01675 | 2.5e-36 | |||||
LMMNOEIH_01676 | 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 | |
LMMNOEIH_01677 | 2.7e-82 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LMMNOEIH_01678 | 8.9e-191 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LMMNOEIH_01679 | 9.3e-57 | 3.4.23.43 | S | Type IV leader peptidase family | ||
LMMNOEIH_01680 | 1.3e-221 | 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 | |
LMMNOEIH_01681 | 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) | |
LMMNOEIH_01682 | 4.9e-81 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
LMMNOEIH_01683 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
LMMNOEIH_01684 | 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 | |
LMMNOEIH_01685 | 0.0 | S | L,D-transpeptidase catalytic domain | |||
LMMNOEIH_01686 | 1.6e-290 | sufB | O | FeS assembly protein SufB | ||
LMMNOEIH_01687 | 6.1e-235 | sufD | O | FeS assembly protein SufD | ||
LMMNOEIH_01688 | 1e-142 | sufC | O | FeS assembly ATPase SufC | ||
LMMNOEIH_01689 | 4.2e-239 | 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 | |
LMMNOEIH_01690 | 3.4e-100 | iscU | C | SUF system FeS assembly protein, NifU family | ||
LMMNOEIH_01691 | 6.1e-108 | yitW | S | Iron-sulfur cluster assembly protein | ||
LMMNOEIH_01692 | 8.1e-243 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
LMMNOEIH_01693 | 2.6e-163 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
LMMNOEIH_01695 | 2e-138 | 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 | |
LMMNOEIH_01696 | 6.9e-56 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
LMMNOEIH_01697 | 1.3e-207 | phoH | T | PhoH-like protein | ||
LMMNOEIH_01698 | 9.4e-103 | 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 | |
LMMNOEIH_01699 | 4.1e-251 | corC | S | CBS domain | ||
LMMNOEIH_01700 | 2e-180 | 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 | ||
LMMNOEIH_01701 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LMMNOEIH_01702 | 1.7e-202 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
LMMNOEIH_01703 | 1.6e-43 | pntAA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
LMMNOEIH_01704 | 3.5e-258 | 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 | |
LMMNOEIH_01705 | 4.2e-269 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01707 | 4.6e-225 | G | Transmembrane secretion effector | |||
LMMNOEIH_01708 | 7e-121 | K | Bacterial regulatory proteins, tetR family | |||
LMMNOEIH_01709 | 1.1e-39 | nrdH | O | Glutaredoxin | ||
LMMNOEIH_01710 | 3.3e-74 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LMMNOEIH_01711 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LMMNOEIH_01713 | 3.1e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LMMNOEIH_01714 | 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 | ||
LMMNOEIH_01715 | 1.3e-29 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01716 | 6.5e-25 | yhjX | EGP | Major facilitator Superfamily | ||
LMMNOEIH_01717 | 3.8e-195 | S | alpha beta | |||
LMMNOEIH_01718 | 1e-89 | 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 | ||
LMMNOEIH_01719 | 9.1e-92 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LMMNOEIH_01720 | 3.2e-54 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LMMNOEIH_01721 | 2.3e-58 | K | Acetyltransferase (GNAT) domain | |||
LMMNOEIH_01723 | 2.5e-227 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
LMMNOEIH_01724 | 1.1e-133 | S | UPF0126 domain | |||
LMMNOEIH_01725 | 2.9e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
LMMNOEIH_01726 | 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 | ||
LMMNOEIH_01727 | 1.5e-233 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LMMNOEIH_01728 | 5e-145 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
LMMNOEIH_01729 | 3.8e-287 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
LMMNOEIH_01730 | 2.1e-218 | luxE | 6.2.1.19 | H | long-chain-fatty-acid--luciferin-component ligase, acyl-protein synthase | |
LMMNOEIH_01731 | 2.5e-234 | F | Psort location CytoplasmicMembrane, score 10.00 | |||
LMMNOEIH_01732 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
LMMNOEIH_01733 | 2.6e-307 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
LMMNOEIH_01734 | 2e-74 | |||||
LMMNOEIH_01735 | 7.6e-249 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
LMMNOEIH_01736 | 1.9e-158 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
LMMNOEIH_01737 | 1.8e-198 | 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 | |
LMMNOEIH_01738 | 4.5e-100 | sixA | 3.6.1.55 | T | Phosphoglycerate mutase family | |
LMMNOEIH_01739 | 2.4e-239 | int | L | Phage integrase, N-terminal SAM-like domain | ||
LMMNOEIH_01740 | 6.3e-25 | S | Predicted membrane protein (DUF2335) | |||
LMMNOEIH_01741 | 5.2e-20 | S | Predicted membrane protein (DUF2335) | |||
LMMNOEIH_01742 | 1e-34 | N | HicA toxin of bacterial toxin-antitoxin, | |||
LMMNOEIH_01743 | 3.7e-54 | S | PFAM Uncharacterised protein family UPF0150 | |||
LMMNOEIH_01744 | 1.9e-86 | |||||
LMMNOEIH_01745 | 1.5e-30 | |||||
LMMNOEIH_01746 | 2.3e-103 | dinD | S | SOS response | ||
LMMNOEIH_01747 | 1.1e-10 | |||||
LMMNOEIH_01752 | 0.0 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LMMNOEIH_01753 | 2.1e-241 | V | ABC transporter permease | |||
LMMNOEIH_01754 | 1.1e-156 | V | ABC transporter | |||
LMMNOEIH_01755 | 5.1e-150 | T | HD domain | |||
LMMNOEIH_01756 | 1e-167 | S | Glutamine amidotransferase domain | |||
LMMNOEIH_01757 | 0.0 | kup | P | Transport of potassium into the cell | ||
LMMNOEIH_01758 | 6.5e-184 | tatD | L | TatD related DNase | ||
LMMNOEIH_01759 | 0.0 | G | Alpha-L-arabinofuranosidase C-terminus | |||
LMMNOEIH_01760 | 1.1e-232 | G | Alpha galactosidase A | |||
LMMNOEIH_01761 | 4.7e-219 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_01762 | 0.0 | rafA | 3.2.1.22 | G | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01763 | 3e-125 | |||||
LMMNOEIH_01764 | 0.0 | yknV | V | ABC transporter | ||
LMMNOEIH_01765 | 0.0 | mdlA2 | V | ABC transporter | ||
LMMNOEIH_01766 | 2.4e-214 | lipA | I | Hydrolase, alpha beta domain protein | ||
LMMNOEIH_01767 | 5e-27 | S | Psort location Cytoplasmic, score 8.87 | |||
LMMNOEIH_01768 | 5.5e-155 | I | alpha/beta hydrolase fold | |||
LMMNOEIH_01769 | 1.8e-236 | M | Protein of unknown function (DUF2961) | |||
LMMNOEIH_01770 | 0.0 | M | probably involved in cell wall | |||
LMMNOEIH_01771 | 1.9e-250 | 3.2.1.14 | GH18 | S | Carbohydrate binding domain | |
LMMNOEIH_01772 | 0.0 | T | Diguanylate cyclase, GGDEF domain | |||
LMMNOEIH_01773 | 1.5e-186 | lacR | K | Transcriptional regulator, LacI family | ||
LMMNOEIH_01774 | 2.5e-234 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
LMMNOEIH_01775 | 7.6e-149 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
LMMNOEIH_01776 | 0.0 | G | Glycosyl hydrolase family 20, domain 2 | |||
LMMNOEIH_01777 | 8.6e-173 | 2.7.1.2 | GK | ROK family | ||
LMMNOEIH_01778 | 4.4e-164 | G | ABC transporter permease | |||
LMMNOEIH_01779 | 7.5e-147 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01780 | 4.2e-242 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01781 | 1.2e-208 | GK | ROK family | |||
LMMNOEIH_01782 | 1.1e-262 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
LMMNOEIH_01783 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01784 | 1.1e-134 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway. Thus, catalyzes the conversion of 4-amino-5-aminomethyl-2-methylpyrimidine to 4-amino- 5-hydroxymethyl-2-methylpyrimidine (HMP) | |
LMMNOEIH_01785 | 0.0 | cbgA_1 | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
LMMNOEIH_01786 | 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 | |
LMMNOEIH_01787 | 2.5e-106 | |||||
LMMNOEIH_01788 | 1.8e-68 | |||||
LMMNOEIH_01789 | 1.4e-190 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LMMNOEIH_01790 | 4.3e-18 | 3.2.1.78 | GH26 | G | Glycosyl hydrolase family 26 | |
LMMNOEIH_01791 | 2.9e-125 | dedA | S | SNARE associated Golgi protein | ||
LMMNOEIH_01793 | 8.7e-130 | S | HAD hydrolase, family IA, variant 3 | |||
LMMNOEIH_01794 | 8.6e-47 | |||||
LMMNOEIH_01795 | 4.5e-115 | hspR | K | transcriptional regulator, MerR family | ||
LMMNOEIH_01796 | 2.1e-159 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
LMMNOEIH_01797 | 2.8e-48 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
LMMNOEIH_01798 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
LMMNOEIH_01799 | 1.3e-145 | S | Mitochondrial biogenesis AIM24 | |||
LMMNOEIH_01800 | 1.6e-112 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
LMMNOEIH_01801 | 3.1e-130 | S | membrane transporter protein | |||
LMMNOEIH_01802 | 3.5e-157 | srtC | 3.4.22.70 | M | Sortase family | |
LMMNOEIH_01803 | 4.5e-191 | K | Psort location Cytoplasmic, score | |||
LMMNOEIH_01804 | 5.1e-81 | traX | S | TraX protein | ||
LMMNOEIH_01805 | 3.9e-51 | traX | S | TraX protein | ||
LMMNOEIH_01806 | 7e-144 | S | HAD-hyrolase-like | |||
LMMNOEIH_01807 | 7.8e-274 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LMMNOEIH_01808 | 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 |
LMMNOEIH_01809 | 9.7e-109 | pepE | 3.4.13.21 | E | Peptidase family S51 | |
LMMNOEIH_01810 | 2.9e-13 | S | Transposon-encoded protein TnpV | |||
LMMNOEIH_01811 | 6.5e-105 | S | Protein of unknown function, DUF624 | |||
LMMNOEIH_01812 | 7.6e-152 | rafG | G | ABC transporter permease | ||
LMMNOEIH_01813 | 3.7e-154 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
LMMNOEIH_01814 | 4.9e-182 | K | Psort location Cytoplasmic, score | |||
LMMNOEIH_01815 | 1.8e-187 | K | Periplasmic binding protein-like domain | |||
LMMNOEIH_01816 | 1.4e-264 | amyE | G | Bacterial extracellular solute-binding protein | ||
LMMNOEIH_01817 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
LMMNOEIH_01818 | 3.3e-247 | amyE | G | Bacterial extracellular solute-binding protein | ||
LMMNOEIH_01819 | 2.4e-135 | G | Phosphoglycerate mutase family | |||
LMMNOEIH_01820 | 1.9e-62 | S | Protein of unknown function (DUF4235) | |||
LMMNOEIH_01821 | 1e-142 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
LMMNOEIH_01822 | 1.6e-44 | |||||
LMMNOEIH_01823 | 1.7e-51 | G | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01824 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
LMMNOEIH_01825 | 2.2e-169 | K | helix_turn _helix lactose operon repressor | |||
LMMNOEIH_01826 | 1.2e-263 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01827 | 6.8e-53 | lacZ5 | 3.2.1.23 | G | beta-galactosidase activity | |
LMMNOEIH_01828 | 3.3e-189 | K | Bacterial regulatory proteins, lacI family | |||
LMMNOEIH_01829 | 1.1e-156 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01830 | 3.3e-175 | P | Binding-protein-dependent transport system inner membrane component | |||
LMMNOEIH_01831 | 4.4e-266 | G | Bacterial extracellular solute-binding protein | |||
LMMNOEIH_01832 | 2e-244 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
LMMNOEIH_01833 | 1.3e-145 | IQ | KR domain | |||
LMMNOEIH_01834 | 4.3e-160 | S | Amidohydrolase | |||
LMMNOEIH_01835 | 4e-167 | dapA | 4.1.2.28, 4.3.3.7 | EM | Dihydrodipicolinate synthetase family | |
LMMNOEIH_01836 | 0.0 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
LMMNOEIH_01837 | 1.4e-181 | lacR | K | Transcriptional regulator, LacI family | ||
LMMNOEIH_01838 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01839 | 3.7e-22 | G | Major facilitator Superfamily | |||
LMMNOEIH_01840 | 4.9e-241 | vex3 | V | ABC transporter permease | ||
LMMNOEIH_01841 | 4.5e-214 | vex1 | V | Efflux ABC transporter, permease protein | ||
LMMNOEIH_01842 | 1.1e-113 | vex2 | V | ABC transporter, ATP-binding protein | ||
LMMNOEIH_01843 | 6.9e-80 | ypeA | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01844 | 4.9e-120 | ybjG | 3.6.1.27 | I | Psort location CytoplasmicMembrane, score | |
LMMNOEIH_01845 | 0.0 | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein | |
LMMNOEIH_01846 | 2.5e-71 | S | GtrA-like protein | |||
LMMNOEIH_01847 | 8.1e-10 | S | LPXTG-motif cell wall anchor domain protein | |||
LMMNOEIH_01848 | 0.0 | S | LPXTG-motif cell wall anchor domain protein | |||
LMMNOEIH_01849 | 4e-279 | M | LPXTG-motif cell wall anchor domain protein | |||
LMMNOEIH_01850 | 1.6e-161 | 3.4.22.70 | M | Sortase family | ||
LMMNOEIH_01851 | 2.6e-138 | |||||
LMMNOEIH_01852 | 8.8e-48 | S | Psort location Cytoplasmic, score | |||
LMMNOEIH_01853 | 2.5e-213 | clcA_2 | P | Voltage gated chloride channel | ||
LMMNOEIH_01854 | 3.9e-57 | |||||
LMMNOEIH_01855 | 5.5e-235 | T | GHKL domain | |||
LMMNOEIH_01856 | 2.8e-131 | K | LytTr DNA-binding domain | |||
LMMNOEIH_01857 | 1.6e-210 | ugpC | E | Belongs to the ABC transporter superfamily | ||
LMMNOEIH_01858 | 2e-269 | KLT | Domain of unknown function (DUF4032) | |||
LMMNOEIH_01859 | 1.2e-175 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LMMNOEIH_01860 | 1.7e-232 | EGP | Major facilitator Superfamily | |||
LMMNOEIH_01861 | 4.5e-13 | S | Psort location Extracellular, score 8.82 | |||
LMMNOEIH_01862 | 1.3e-54 | DJ | Addiction module toxin, RelE StbE family | |||
LMMNOEIH_01863 | 5.9e-49 | S | Antitoxin component of a toxin-antitoxin (TA) module | |||
LMMNOEIH_01864 | 2.7e-115 | S | Short repeat of unknown function (DUF308) | |||
LMMNOEIH_01865 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LMMNOEIH_01866 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
LMMNOEIH_01867 | 1.8e-83 | K | Cro/C1-type HTH DNA-binding domain | |||
LMMNOEIH_01868 | 4e-26 | S | phage tail tape measure protein | |||
LMMNOEIH_01869 | 8.9e-88 | S | phage tail tape measure protein | |||
LMMNOEIH_01871 | 8.6e-63 | |||||
LMMNOEIH_01872 | 1.1e-110 | |||||
LMMNOEIH_01873 | 1.7e-61 | |||||
LMMNOEIH_01874 | 4.7e-35 | |||||
LMMNOEIH_01875 | 1e-43 | |||||
LMMNOEIH_01876 | 2.5e-65 | S | Phage protein Gp19/Gp15/Gp42 | |||
LMMNOEIH_01878 | 4.2e-153 | V | Phage capsid family | |||
LMMNOEIH_01879 | 3.1e-71 | |||||
LMMNOEIH_01881 | 2.8e-113 | |||||
LMMNOEIH_01882 | 7.5e-243 | S | Phage portal protein, SPP1 Gp6-like | |||
LMMNOEIH_01883 | 1.4e-227 | S | Terminase | |||
LMMNOEIH_01884 | 3.2e-37 | |||||
LMMNOEIH_01885 | 6.6e-51 | V | HNH nucleases | |||
LMMNOEIH_01886 | 6.1e-165 | J | tRNA 5'-leader removal | |||
LMMNOEIH_01887 | 2.2e-16 | |||||
LMMNOEIH_01890 | 1.2e-10 | |||||
LMMNOEIH_01893 | 1.2e-103 | A | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | |||
LMMNOEIH_01894 | 1.1e-76 | V | HNH endonuclease | |||
LMMNOEIH_01895 | 4.7e-25 | |||||
LMMNOEIH_01896 | 4.8e-136 | K | Transcriptional regulator | |||
LMMNOEIH_01898 | 4.4e-63 | ssb1 | L | Single-strand binding protein family | ||
LMMNOEIH_01903 | 8.5e-37 | |||||
LMMNOEIH_01905 | 1.9e-73 | K | BRO family, N-terminal domain |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)