ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
FEAFEJEJ_00001 | 7.6e-56 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_00002 | 4.9e-79 | |||||
FEAFEJEJ_00003 | 8.2e-63 | K | Transcriptional regulator, HxlR family | |||
FEAFEJEJ_00004 | 1.5e-201 | ytbD | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_00005 | 9.4e-183 | S | Aldo keto reductase | |||
FEAFEJEJ_00006 | 1.8e-136 | cysA | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00007 | 0.0 | Q | FtsX-like permease family | |||
FEAFEJEJ_00008 | 3.5e-61 | gntR1 | K | Transcriptional regulator, GntR family | ||
FEAFEJEJ_00009 | 2.7e-70 | S | Iron-sulphur cluster biosynthesis | |||
FEAFEJEJ_00010 | 1.6e-188 | sdrF | M | Collagen binding domain | ||
FEAFEJEJ_00011 | 0.0 | cadA | P | P-type ATPase | ||
FEAFEJEJ_00012 | 5.2e-119 | S | SNARE associated Golgi protein | |||
FEAFEJEJ_00013 | 0.0 | mco | Q | Multicopper oxidase | ||
FEAFEJEJ_00014 | 1.6e-52 | czrA | K | Transcriptional regulator, ArsR family | ||
FEAFEJEJ_00015 | 4.8e-100 | P | Cadmium resistance transporter | |||
FEAFEJEJ_00016 | 6e-159 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
FEAFEJEJ_00017 | 6.1e-152 | K | LysR substrate binding domain | |||
FEAFEJEJ_00018 | 3.9e-210 | norA | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_00019 | 1.1e-158 | K | helix_turn_helix, arabinose operon control protein | |||
FEAFEJEJ_00020 | 9e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00021 | 1e-81 | ydjP | I | Alpha/beta hydrolase family | ||
FEAFEJEJ_00022 | 2.4e-109 | citR | K | Putative sugar-binding domain | ||
FEAFEJEJ_00023 | 1.8e-151 | mez_1 | 1.1.1.38 | C | Malic enzyme, NAD binding domain | |
FEAFEJEJ_00024 | 7.5e-135 | mleP | S | Membrane transport protein | ||
FEAFEJEJ_00025 | 5.1e-112 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
FEAFEJEJ_00026 | 1.1e-30 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
FEAFEJEJ_00027 | 3.3e-145 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
FEAFEJEJ_00028 | 1.3e-258 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
FEAFEJEJ_00029 | 9.5e-47 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
FEAFEJEJ_00030 | 3.2e-97 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
FEAFEJEJ_00031 | 5e-165 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
FEAFEJEJ_00032 | 8.7e-181 | xopQ | 3.2.2.1, 3.2.2.8 | F | inosine-uridine preferring nucleoside hydrolase | |
FEAFEJEJ_00033 | 1.4e-25 | |||||
FEAFEJEJ_00034 | 0.0 | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | ||
FEAFEJEJ_00035 | 3.2e-135 | XK27_07210 | 6.1.1.6 | S | B3/4 domain | |
FEAFEJEJ_00036 | 1.9e-127 | S | Protein of unknown function (DUF975) | |||
FEAFEJEJ_00037 | 7.2e-62 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
FEAFEJEJ_00038 | 1.7e-162 | ytrB | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00039 | 8.4e-176 | |||||
FEAFEJEJ_00040 | 1.3e-193 | KT | Putative sugar diacid recognition | |||
FEAFEJEJ_00041 | 9.7e-215 | EG | GntP family permease | |||
FEAFEJEJ_00042 | 2e-208 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
FEAFEJEJ_00043 | 5.8e-269 | ydbT | S | Bacterial PH domain | ||
FEAFEJEJ_00044 | 1.7e-84 | S | Bacterial PH domain | |||
FEAFEJEJ_00045 | 4.9e-78 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
FEAFEJEJ_00046 | 1.6e-255 | U | Belongs to the purine-cytosine permease (2.A.39) family | |||
FEAFEJEJ_00047 | 9.8e-36 | |||||
FEAFEJEJ_00048 | 4.1e-278 | frvR | K | Mga helix-turn-helix domain | ||
FEAFEJEJ_00049 | 6.1e-252 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
FEAFEJEJ_00050 | 1.6e-61 | K | Winged helix DNA-binding domain | |||
FEAFEJEJ_00051 | 4.5e-30 | |||||
FEAFEJEJ_00052 | 4.1e-240 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
FEAFEJEJ_00053 | 5.8e-241 | 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) | |
FEAFEJEJ_00055 | 1.9e-97 | I | NUDIX domain | |||
FEAFEJEJ_00056 | 2.8e-114 | yviA | S | Protein of unknown function (DUF421) | ||
FEAFEJEJ_00057 | 4.4e-74 | S | Protein of unknown function (DUF3290) | |||
FEAFEJEJ_00058 | 3e-167 | ropB | K | Helix-turn-helix XRE-family like proteins | ||
FEAFEJEJ_00059 | 6.3e-219 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_00060 | 3.2e-253 | gshR | 1.8.1.7 | C | Glutathione reductase | |
FEAFEJEJ_00061 | 9.1e-36 | ygbF | S | Sugar efflux transporter for intercellular exchange | ||
FEAFEJEJ_00062 | 2.2e-193 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00063 | 7.5e-198 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
FEAFEJEJ_00064 | 1e-35 | |||||
FEAFEJEJ_00065 | 1.6e-137 | kguE | 2.7.1.45 | G | Xylose isomerase domain protein TIM barrel | |
FEAFEJEJ_00066 | 8.2e-233 | gntT | EG | Citrate transporter | ||
FEAFEJEJ_00067 | 5.4e-178 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
FEAFEJEJ_00068 | 1e-105 | hxlA | 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase HUMPS family | |
FEAFEJEJ_00069 | 2.7e-86 | hxlB | 4.1.2.14, 4.1.2.43, 4.1.3.42, 5.3.1.27 | M | sugar phosphate isomerase involved in capsule formation | |
FEAFEJEJ_00070 | 5.2e-176 | kdgR | K | helix_turn _helix lactose operon repressor | ||
FEAFEJEJ_00071 | 4.1e-175 | L | Integrase core domain | |||
FEAFEJEJ_00072 | 4.3e-55 | |||||
FEAFEJEJ_00073 | 1.4e-83 | |||||
FEAFEJEJ_00074 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
FEAFEJEJ_00075 | 1.2e-191 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FEAFEJEJ_00076 | 5.7e-169 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
FEAFEJEJ_00077 | 6.3e-227 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
FEAFEJEJ_00078 | 4.9e-179 | |||||
FEAFEJEJ_00079 | 1.8e-130 | cobB | K | SIR2 family | ||
FEAFEJEJ_00080 | 3.8e-51 | |||||
FEAFEJEJ_00081 | 2.8e-162 | yunF | F | Protein of unknown function DUF72 | ||
FEAFEJEJ_00082 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
FEAFEJEJ_00083 | 8.8e-147 | tatD | L | hydrolase, TatD family | ||
FEAFEJEJ_00084 | 4.3e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
FEAFEJEJ_00085 | 5e-162 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
FEAFEJEJ_00086 | 4.3e-36 | veg | S | Biofilm formation stimulator VEG | ||
FEAFEJEJ_00087 | 1.9e-163 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
FEAFEJEJ_00088 | 4.2e-109 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
FEAFEJEJ_00089 | 0.0 | yicI | 3.2.1.177 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
FEAFEJEJ_00090 | 4.8e-260 | xylP | G | MFS/sugar transport protein | ||
FEAFEJEJ_00091 | 9e-212 | xylR | GK | ROK family | ||
FEAFEJEJ_00092 | 2.4e-294 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
FEAFEJEJ_00093 | 1.4e-167 | 2.7.1.2 | GK | ROK family | ||
FEAFEJEJ_00094 | 7.4e-91 | |||||
FEAFEJEJ_00095 | 2.2e-54 | V | Transport permease protein | |||
FEAFEJEJ_00096 | 3.5e-88 | V | ABC transporter | |||
FEAFEJEJ_00097 | 4.2e-85 | KTV | abc transporter atp-binding protein | |||
FEAFEJEJ_00098 | 1.6e-153 | S | Prolyl oligopeptidase family | |||
FEAFEJEJ_00099 | 5.7e-169 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
FEAFEJEJ_00100 | 6.1e-131 | fhuC | P | ABC transporter | ||
FEAFEJEJ_00101 | 8.2e-132 | znuB | U | ABC 3 transport family | ||
FEAFEJEJ_00104 | 4.4e-144 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
FEAFEJEJ_00105 | 3.8e-217 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
FEAFEJEJ_00106 | 5.5e-178 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
FEAFEJEJ_00107 | 9.7e-56 | S | Domain of unknown function (DUF3899) | |||
FEAFEJEJ_00108 | 7.2e-71 | racA | K | helix_turn_helix, mercury resistance | ||
FEAFEJEJ_00109 | 5.8e-132 | gntR | K | UbiC transcription regulator-associated domain protein | ||
FEAFEJEJ_00110 | 0.0 | xpkA | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
FEAFEJEJ_00111 | 2.7e-146 | yxeH | S | hydrolase | ||
FEAFEJEJ_00112 | 1.3e-267 | ywfO | S | HD domain protein | ||
FEAFEJEJ_00113 | 4.3e-155 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
FEAFEJEJ_00114 | 1.7e-78 | ywiB | S | Domain of unknown function (DUF1934) | ||
FEAFEJEJ_00115 | 5.8e-54 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
FEAFEJEJ_00116 | 6.7e-311 | 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 | |
FEAFEJEJ_00117 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
FEAFEJEJ_00118 | 2.9e-227 | |||||
FEAFEJEJ_00119 | 3e-72 | K | Transcriptional regulator | |||
FEAFEJEJ_00120 | 4.6e-311 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
FEAFEJEJ_00121 | 4e-130 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
FEAFEJEJ_00122 | 0.0 | pelX | UW | LPXTG-motif cell wall anchor domain protein | ||
FEAFEJEJ_00123 | 2.8e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
FEAFEJEJ_00124 | 4.3e-42 | rpmE2 | J | Ribosomal protein L31 | ||
FEAFEJEJ_00125 | 8.7e-117 | srtA | 3.4.22.70 | M | sortase family | |
FEAFEJEJ_00126 | 5.7e-18 | S | WxL domain surface cell wall-binding | |||
FEAFEJEJ_00127 | 2.7e-07 | S | WxL domain surface cell wall-binding | |||
FEAFEJEJ_00128 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00130 | 4.8e-110 | XK27_00720 | S | regulation of response to stimulus | ||
FEAFEJEJ_00131 | 2.5e-252 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
FEAFEJEJ_00132 | 5.3e-86 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
FEAFEJEJ_00133 | 9.9e-95 | lemA | S | LemA family | ||
FEAFEJEJ_00134 | 1.6e-147 | htpX | O | Belongs to the peptidase M48B family | ||
FEAFEJEJ_00135 | 8.6e-150 | |||||
FEAFEJEJ_00136 | 2.4e-256 | 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 | |
FEAFEJEJ_00137 | 1.6e-240 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
FEAFEJEJ_00138 | 2.1e-213 | S | nuclear-transcribed mRNA catabolic process, no-go decay | |||
FEAFEJEJ_00139 | 2.9e-63 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
FEAFEJEJ_00140 | 1.4e-214 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
FEAFEJEJ_00142 | 3.6e-61 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
FEAFEJEJ_00143 | 4e-113 | S | (CBS) domain | |||
FEAFEJEJ_00145 | 1.9e-256 | S | Putative peptidoglycan binding domain | |||
FEAFEJEJ_00146 | 2.2e-176 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
FEAFEJEJ_00147 | 8.7e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
FEAFEJEJ_00148 | 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 | ||
FEAFEJEJ_00149 | 1.4e-295 | yabM | S | Polysaccharide biosynthesis protein | ||
FEAFEJEJ_00150 | 6.2e-39 | yabO | J | S4 domain protein | ||
FEAFEJEJ_00151 | 9.7e-44 | divIC | D | Septum formation initiator | ||
FEAFEJEJ_00152 | 4.2e-71 | yabR | J | RNA binding | ||
FEAFEJEJ_00153 | 5.7e-258 | 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 | |
FEAFEJEJ_00154 | 1.3e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
FEAFEJEJ_00155 | 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 | ||
FEAFEJEJ_00156 | 2.6e-163 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
FEAFEJEJ_00157 | 4.8e-193 | 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 | ||
FEAFEJEJ_00162 | 9.9e-52 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
FEAFEJEJ_00163 | 3e-298 | dtpT | U | amino acid peptide transporter | ||
FEAFEJEJ_00164 | 1.2e-148 | yjjH | S | Calcineurin-like phosphoesterase | ||
FEAFEJEJ_00167 | 6.6e-137 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
FEAFEJEJ_00168 | 7e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
FEAFEJEJ_00169 | 1.9e-124 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
FEAFEJEJ_00170 | 5.3e-92 | MA20_25245 | K | FR47-like protein | ||
FEAFEJEJ_00171 | 5.3e-141 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
FEAFEJEJ_00172 | 4.8e-287 | 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 | |
FEAFEJEJ_00173 | 6.1e-154 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
FEAFEJEJ_00174 | 1.4e-72 | |||||
FEAFEJEJ_00175 | 0.0 | yhgF | K | Tex-like protein N-terminal domain protein | ||
FEAFEJEJ_00176 | 4e-89 | ydcK | S | Belongs to the SprT family | ||
FEAFEJEJ_00177 | 4.1e-156 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
FEAFEJEJ_00179 | 3.1e-47 | 4.1.1.52, 4.2.1.83 | E | amidohydrolase | ||
FEAFEJEJ_00180 | 5.5e-18 | yobS | K | transcriptional regulator | ||
FEAFEJEJ_00181 | 4.7e-100 | S | Psort location CytoplasmicMembrane, score | |||
FEAFEJEJ_00182 | 6.6e-75 | K | MarR family | |||
FEAFEJEJ_00183 | 3e-246 | dinF | V | MatE | ||
FEAFEJEJ_00184 | 1.8e-110 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant | |
FEAFEJEJ_00185 | 9.6e-55 | manL | 2.7.1.191 | G | PTS system fructose IIA component | |
FEAFEJEJ_00186 | 6.9e-60 | pts10B | 2.7.1.191, 2.7.1.202 | G | PTS system sorbose subfamily IIB component | |
FEAFEJEJ_00187 | 1.1e-117 | manM | G | PTS system | ||
FEAFEJEJ_00188 | 2.5e-155 | manN | G | system, mannose fructose sorbose family IID component | ||
FEAFEJEJ_00189 | 1.7e-177 | K | AI-2E family transporter | |||
FEAFEJEJ_00190 | 2.7e-168 | 2.7.7.65 | T | diguanylate cyclase | ||
FEAFEJEJ_00191 | 1.9e-118 | yliE | T | EAL domain | ||
FEAFEJEJ_00192 | 2.8e-102 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_00193 | 2e-212 | XK27_06930 | V | domain protein | ||
FEAFEJEJ_00194 | 1.9e-169 | znuA | P | Belongs to the bacterial solute-binding protein 9 family | ||
FEAFEJEJ_00195 | 7.8e-205 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
FEAFEJEJ_00196 | 6.1e-166 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
FEAFEJEJ_00197 | 1.3e-174 | EG | EamA-like transporter family | |||
FEAFEJEJ_00198 | 1.5e-123 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
FEAFEJEJ_00199 | 1.3e-229 | V | Beta-lactamase | |||
FEAFEJEJ_00200 | 5e-259 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
FEAFEJEJ_00202 | 5.3e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
FEAFEJEJ_00203 | 4.1e-56 | |||||
FEAFEJEJ_00204 | 8.7e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
FEAFEJEJ_00205 | 1.1e-256 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
FEAFEJEJ_00206 | 3.7e-213 | yacL | S | domain protein | ||
FEAFEJEJ_00207 | 1.2e-288 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
FEAFEJEJ_00208 | 7.4e-277 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FEAFEJEJ_00209 | 7.8e-70 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
FEAFEJEJ_00210 | 2.5e-138 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
FEAFEJEJ_00211 | 1.8e-90 | yacP | S | YacP-like NYN domain | ||
FEAFEJEJ_00212 | 1.5e-98 | sigH | K | Sigma-70 region 2 | ||
FEAFEJEJ_00213 | 2.7e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
FEAFEJEJ_00214 | 3.3e-25 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
FEAFEJEJ_00215 | 1.1e-98 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
FEAFEJEJ_00216 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
FEAFEJEJ_00217 | 1.2e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
FEAFEJEJ_00218 | 6.9e-84 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
FEAFEJEJ_00219 | 4e-49 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
FEAFEJEJ_00220 | 7.7e-174 | L | Integrase core domain | |||
FEAFEJEJ_00221 | 0.0 | mprF | 2.3.2.3 | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
FEAFEJEJ_00222 | 4.2e-109 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
FEAFEJEJ_00223 | 4.6e-171 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
FEAFEJEJ_00224 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_00225 | 8.5e-195 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
FEAFEJEJ_00226 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
FEAFEJEJ_00227 | 4.9e-37 | nrdH | O | Glutaredoxin | ||
FEAFEJEJ_00228 | 3.1e-91 | rsmC | 2.1.1.172 | J | Methyltransferase | |
FEAFEJEJ_00229 | 1.1e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
FEAFEJEJ_00230 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
FEAFEJEJ_00231 | 3.6e-38 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
FEAFEJEJ_00232 | 4.3e-101 | 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 | ||
FEAFEJEJ_00233 | 1.3e-38 | yaaL | S | Protein of unknown function (DUF2508) | ||
FEAFEJEJ_00234 | 2.1e-112 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
FEAFEJEJ_00235 | 2.2e-54 | yaaQ | S | Cyclic-di-AMP receptor | ||
FEAFEJEJ_00236 | 3.2e-181 | holB | 2.7.7.7 | L | DNA polymerase III | |
FEAFEJEJ_00237 | 1.7e-38 | yabA | L | Involved in initiation control of chromosome replication | ||
FEAFEJEJ_00238 | 2.6e-163 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
FEAFEJEJ_00239 | 4e-141 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
FEAFEJEJ_00240 | 3.2e-127 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
FEAFEJEJ_00241 | 1.8e-110 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
FEAFEJEJ_00242 | 1.4e-195 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
FEAFEJEJ_00243 | 1.1e-214 | yeaN | P | Transporter, major facilitator family protein | ||
FEAFEJEJ_00244 | 7.5e-46 | cadC1 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
FEAFEJEJ_00245 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00246 | 6.9e-113 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
FEAFEJEJ_00247 | 3e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
FEAFEJEJ_00248 | 6.5e-293 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
FEAFEJEJ_00249 | 0.0 | ydaO | E | amino acid | ||
FEAFEJEJ_00250 | 3.7e-140 | lrgB | M | LrgB-like family | ||
FEAFEJEJ_00251 | 1.6e-60 | lrgA | S | LrgA family | ||
FEAFEJEJ_00252 | 3.6e-178 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
FEAFEJEJ_00253 | 1.1e-116 | yvyE | 3.4.13.9 | S | YigZ family | |
FEAFEJEJ_00254 | 1.5e-255 | comFA | L | Helicase C-terminal domain protein | ||
FEAFEJEJ_00255 | 1.1e-124 | comFC | S | Competence protein | ||
FEAFEJEJ_00256 | 7.9e-97 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
FEAFEJEJ_00257 | 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 | ||
FEAFEJEJ_00258 | 4.7e-185 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
FEAFEJEJ_00259 | 4.3e-222 | minJ | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
FEAFEJEJ_00260 | 7.6e-129 | K | response regulator | |||
FEAFEJEJ_00261 | 3.1e-248 | phoR | 2.7.13.3 | T | Histidine kinase | |
FEAFEJEJ_00262 | 9.1e-189 | L | Helix-turn-helix domain | |||
FEAFEJEJ_00263 | 2.5e-161 | pstS | P | Phosphate | ||
FEAFEJEJ_00264 | 2e-158 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
FEAFEJEJ_00265 | 5.9e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
FEAFEJEJ_00266 | 6.9e-150 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
FEAFEJEJ_00267 | 3.5e-140 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
FEAFEJEJ_00268 | 1.4e-119 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
FEAFEJEJ_00269 | 1.7e-54 | pspC | KT | PspC domain protein | ||
FEAFEJEJ_00270 | 5.5e-30 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
FEAFEJEJ_00271 | 2.8e-171 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
FEAFEJEJ_00272 | 1.1e-150 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
FEAFEJEJ_00273 | 1.5e-183 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
FEAFEJEJ_00274 | 5.6e-169 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
FEAFEJEJ_00275 | 4.5e-177 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
FEAFEJEJ_00277 | 6.7e-116 | yfbR | S | HD containing hydrolase-like enzyme | ||
FEAFEJEJ_00278 | 4.5e-94 | K | acetyltransferase | |||
FEAFEJEJ_00279 | 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 | ||
FEAFEJEJ_00280 | 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 | ||
FEAFEJEJ_00281 | 2.4e-90 | S | Short repeat of unknown function (DUF308) | |||
FEAFEJEJ_00282 | 4.8e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
FEAFEJEJ_00283 | 3.4e-191 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
FEAFEJEJ_00284 | 9.9e-169 | whiA | K | May be required for sporulation | ||
FEAFEJEJ_00285 | 1.7e-102 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
FEAFEJEJ_00286 | 2.6e-74 | XK27_02470 | K | LytTr DNA-binding domain | ||
FEAFEJEJ_00287 | 1.6e-126 | liaI | S | membrane | ||
FEAFEJEJ_00289 | 1.4e-107 | S | ECF transporter, substrate-specific component | |||
FEAFEJEJ_00291 | 7.5e-186 | cggR | K | Putative sugar-binding domain | ||
FEAFEJEJ_00292 | 9e-192 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
FEAFEJEJ_00293 | 4.3e-225 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
FEAFEJEJ_00294 | 2.3e-139 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
FEAFEJEJ_00295 | 6.1e-249 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
FEAFEJEJ_00297 | 1.8e-284 | clcA | P | chloride | ||
FEAFEJEJ_00298 | 4.9e-32 | secG | U | Preprotein translocase | ||
FEAFEJEJ_00299 | 7.1e-141 | est | 3.1.1.1 | S | Serine aminopeptidase, S33 | |
FEAFEJEJ_00300 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
FEAFEJEJ_00301 | 2.3e-81 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
FEAFEJEJ_00302 | 5.8e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
FEAFEJEJ_00303 | 1.4e-175 | L | Integrase core domain | |||
FEAFEJEJ_00304 | 1.3e-102 | yxjI | ||||
FEAFEJEJ_00305 | 1.8e-141 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
FEAFEJEJ_00306 | 1.1e-178 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
FEAFEJEJ_00307 | 1.9e-83 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
FEAFEJEJ_00308 | 1.4e-87 | 2.3.1.128, 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
FEAFEJEJ_00309 | 3e-195 | C | Aldo keto reductase family protein | |||
FEAFEJEJ_00310 | 6e-102 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
FEAFEJEJ_00311 | 2.4e-152 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
FEAFEJEJ_00312 | 5e-165 | murB | 1.3.1.98 | M | Cell wall formation | |
FEAFEJEJ_00313 | 0.0 | yjcE | P | Sodium proton antiporter | ||
FEAFEJEJ_00314 | 1.2e-123 | S | Protein of unknown function (DUF1361) | |||
FEAFEJEJ_00315 | 4.5e-152 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
FEAFEJEJ_00316 | 1.8e-133 | ybbR | S | YbbR-like protein | ||
FEAFEJEJ_00317 | 1.1e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
FEAFEJEJ_00318 | 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 | |
FEAFEJEJ_00319 | 1.7e-12 | |||||
FEAFEJEJ_00320 | 9.1e-130 | 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 | |
FEAFEJEJ_00321 | 5.2e-254 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
FEAFEJEJ_00322 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
FEAFEJEJ_00323 | 4.1e-98 | dps | P | Belongs to the Dps family | ||
FEAFEJEJ_00324 | 1.1e-25 | copZ | P | Heavy-metal-associated domain | ||
FEAFEJEJ_00325 | 8.7e-201 | tagH | 3.6.3.38, 3.6.3.40 | GM | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
FEAFEJEJ_00326 | 3.1e-50 | |||||
FEAFEJEJ_00327 | 2e-87 | S | Iron Transport-associated domain | |||
FEAFEJEJ_00328 | 1.8e-178 | M | Iron Transport-associated domain | |||
FEAFEJEJ_00329 | 4.4e-90 | M | Iron Transport-associated domain | |||
FEAFEJEJ_00330 | 1.2e-163 | isdE | P | Periplasmic binding protein | ||
FEAFEJEJ_00331 | 1.4e-170 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
FEAFEJEJ_00332 | 7.1e-141 | fhuC | 3.6.3.34 | HP | ABC transporter, ATP-binding protein | |
FEAFEJEJ_00333 | 2.4e-170 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
FEAFEJEJ_00334 | 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) | |
FEAFEJEJ_00335 | 6.4e-290 | ppx3 | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
FEAFEJEJ_00336 | 1.6e-151 | licD | M | LicD family | ||
FEAFEJEJ_00337 | 6.4e-78 | S | Domain of unknown function (DUF5067) | |||
FEAFEJEJ_00338 | 2.3e-75 | K | Transcriptional regulator | |||
FEAFEJEJ_00339 | 1.9e-25 | |||||
FEAFEJEJ_00340 | 2.7e-79 | O | OsmC-like protein | |||
FEAFEJEJ_00341 | 8.3e-24 | |||||
FEAFEJEJ_00343 | 2e-56 | ypaA | S | Protein of unknown function (DUF1304) | ||
FEAFEJEJ_00344 | 4.1e-89 | |||||
FEAFEJEJ_00345 | 3.8e-257 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
FEAFEJEJ_00346 | 6.7e-259 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
FEAFEJEJ_00347 | 6e-95 | K | helix_turn _helix lactose operon repressor | |||
FEAFEJEJ_00348 | 9.8e-103 | S | Putative glutamine amidotransferase | |||
FEAFEJEJ_00349 | 1.3e-134 | S | protein conserved in bacteria | |||
FEAFEJEJ_00350 | 1.6e-151 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
FEAFEJEJ_00351 | 7.7e-238 | arcA | 3.5.3.6 | E | Arginine | |
FEAFEJEJ_00352 | 1.3e-45 | |||||
FEAFEJEJ_00355 | 2e-146 | K | response regulator | |||
FEAFEJEJ_00356 | 1.5e-267 | T | PhoQ Sensor | |||
FEAFEJEJ_00357 | 4.9e-210 | ywbD | 2.1.1.191 | J | S-adenosylmethionine-dependent methyltransferase | |
FEAFEJEJ_00358 | 1.9e-153 | glcU | U | sugar transport | ||
FEAFEJEJ_00359 | 7.1e-261 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
FEAFEJEJ_00360 | 0.0 | S | Bacterial membrane protein YfhO | |||
FEAFEJEJ_00361 | 5.2e-81 | tspO | T | TspO/MBR family | ||
FEAFEJEJ_00362 | 3.8e-99 | S | Protein of unknown function (DUF1211) | |||
FEAFEJEJ_00365 | 2e-203 | sip | L | Belongs to the 'phage' integrase family | ||
FEAFEJEJ_00369 | 1.7e-07 | |||||
FEAFEJEJ_00370 | 3.8e-121 | L | DNA replication protein | |||
FEAFEJEJ_00371 | 5.7e-245 | S | Virulence-associated protein E | |||
FEAFEJEJ_00372 | 7.3e-55 | |||||
FEAFEJEJ_00374 | 5.3e-19 | S | head-tail joining protein | |||
FEAFEJEJ_00375 | 2.4e-52 | L | HNH endonuclease | |||
FEAFEJEJ_00376 | 8.5e-76 | terS | L | Phage terminase, small subunit | ||
FEAFEJEJ_00377 | 2.6e-308 | terL | S | overlaps another CDS with the same product name | ||
FEAFEJEJ_00379 | 3e-193 | S | Phage portal protein | |||
FEAFEJEJ_00380 | 3.2e-273 | S | Caudovirus prohead serine protease | |||
FEAFEJEJ_00381 | 2.1e-31 | S | Phage gp6-like head-tail connector protein | |||
FEAFEJEJ_00382 | 1.7e-42 | |||||
FEAFEJEJ_00383 | 5.6e-29 | cspA | K | Cold shock protein | ||
FEAFEJEJ_00384 | 4e-28 | |||||
FEAFEJEJ_00385 | 5.8e-164 | S | NAD:arginine ADP-ribosyltransferase | |||
FEAFEJEJ_00386 | 2.2e-199 | ybiR | P | Citrate transporter | ||
FEAFEJEJ_00387 | 4.9e-122 | yliE | T | Putative diguanylate phosphodiesterase | ||
FEAFEJEJ_00388 | 1.1e-150 | 2.7.7.65 | T | diguanylate cyclase | ||
FEAFEJEJ_00389 | 8.7e-09 | |||||
FEAFEJEJ_00390 | 3.6e-224 | L | Transposase | |||
FEAFEJEJ_00391 | 6.6e-173 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00392 | 8.9e-56 | |||||
FEAFEJEJ_00393 | 0.0 | lmrA | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00394 | 0.0 | yfiC | V | ABC transporter | ||
FEAFEJEJ_00395 | 9.3e-197 | ampC | V | Beta-lactamase | ||
FEAFEJEJ_00396 | 5.6e-132 | cobQ | S | glutamine amidotransferase | ||
FEAFEJEJ_00397 | 1.4e-264 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain | |
FEAFEJEJ_00398 | 8.5e-110 | tdk | 2.7.1.21 | F | thymidine kinase | |
FEAFEJEJ_00399 | 5.5e-187 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
FEAFEJEJ_00400 | 7.9e-157 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
FEAFEJEJ_00401 | 1.9e-189 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
FEAFEJEJ_00402 | 5.4e-231 | 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 | |
FEAFEJEJ_00403 | 3e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
FEAFEJEJ_00404 | 6.1e-126 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
FEAFEJEJ_00405 | 7.3e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
FEAFEJEJ_00406 | 1.6e-51 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
FEAFEJEJ_00407 | 2e-89 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
FEAFEJEJ_00408 | 3e-287 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
FEAFEJEJ_00409 | 7.3e-161 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
FEAFEJEJ_00410 | 1.4e-267 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
FEAFEJEJ_00411 | 8.3e-67 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
FEAFEJEJ_00412 | 4.3e-33 | ywzB | S | Protein of unknown function (DUF1146) | ||
FEAFEJEJ_00413 | 5.9e-244 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
FEAFEJEJ_00414 | 4.6e-180 | mbl | D | Cell shape determining protein MreB Mrl | ||
FEAFEJEJ_00415 | 1.1e-52 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
FEAFEJEJ_00416 | 1.1e-33 | S | Protein of unknown function (DUF2969) | |||
FEAFEJEJ_00417 | 1.1e-220 | rodA | D | Belongs to the SEDS family | ||
FEAFEJEJ_00418 | 1.9e-49 | gcsH2 | E | glycine cleavage | ||
FEAFEJEJ_00419 | 9.3e-142 | f42a | O | Band 7 protein | ||
FEAFEJEJ_00420 | 4.2e-178 | S | Protein of unknown function (DUF2785) | |||
FEAFEJEJ_00421 | 1.8e-217 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
FEAFEJEJ_00422 | 1.1e-305 | glpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
FEAFEJEJ_00423 | 7.9e-160 | 2.3.1.19 | K | Helix-turn-helix XRE-family like proteins | ||
FEAFEJEJ_00424 | 1e-81 | usp6 | T | universal stress protein | ||
FEAFEJEJ_00425 | 3.2e-41 | |||||
FEAFEJEJ_00426 | 2.1e-238 | rarA | L | recombination factor protein RarA | ||
FEAFEJEJ_00427 | 1.9e-80 | yueI | S | Protein of unknown function (DUF1694) | ||
FEAFEJEJ_00428 | 1.3e-113 | yktB | S | Belongs to the UPF0637 family | ||
FEAFEJEJ_00429 | 7.1e-61 | KLT | serine threonine protein kinase | |||
FEAFEJEJ_00430 | 9.7e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
FEAFEJEJ_00431 | 3.5e-82 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
FEAFEJEJ_00432 | 0.0 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
FEAFEJEJ_00433 | 3.8e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
FEAFEJEJ_00434 | 4.2e-228 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
FEAFEJEJ_00435 | 1.1e-89 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
FEAFEJEJ_00436 | 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 | |
FEAFEJEJ_00437 | 2.1e-249 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
FEAFEJEJ_00438 | 5.6e-118 | radC | L | DNA repair protein | ||
FEAFEJEJ_00439 | 9.6e-162 | mreB | D | cell shape determining protein MreB | ||
FEAFEJEJ_00440 | 9.7e-139 | mreC | M | Involved in formation and maintenance of cell shape | ||
FEAFEJEJ_00441 | 3.2e-92 | mreD | M | rod shape-determining protein MreD | ||
FEAFEJEJ_00442 | 2.8e-117 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
FEAFEJEJ_00443 | 4.1e-147 | minD | D | Belongs to the ParA family | ||
FEAFEJEJ_00444 | 2.5e-110 | glnP | P | ABC transporter permease | ||
FEAFEJEJ_00445 | 3.5e-93 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
FEAFEJEJ_00446 | 1.3e-159 | aatB | ET | ABC transporter substrate-binding protein | ||
FEAFEJEJ_00447 | 3.4e-236 | ymfF | S | Peptidase M16 inactive domain protein | ||
FEAFEJEJ_00448 | 2.8e-246 | ymfH | S | Peptidase M16 | ||
FEAFEJEJ_00449 | 2.6e-65 | ymfM | S | Domain of unknown function (DUF4115) | ||
FEAFEJEJ_00450 | 1e-99 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
FEAFEJEJ_00451 | 1.6e-227 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
FEAFEJEJ_00452 | 1e-188 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
FEAFEJEJ_00453 | 1.6e-230 | L | Transposase | |||
FEAFEJEJ_00455 | 4e-223 | rny | S | Endoribonuclease that initiates mRNA decay | ||
FEAFEJEJ_00456 | 1.3e-150 | ymdB | S | YmdB-like protein | ||
FEAFEJEJ_00457 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
FEAFEJEJ_00458 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
FEAFEJEJ_00459 | 3.7e-108 | 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 | |
FEAFEJEJ_00460 | 6.5e-190 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
FEAFEJEJ_00461 | 4.1e-200 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
FEAFEJEJ_00462 | 1.2e-227 | 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) | |
FEAFEJEJ_00463 | 1.5e-25 | yajC | U | Preprotein translocase | ||
FEAFEJEJ_00464 | 3e-180 | 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 | |
FEAFEJEJ_00465 | 9.9e-180 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
FEAFEJEJ_00466 | 6.1e-252 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
FEAFEJEJ_00467 | 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 | |
FEAFEJEJ_00468 | 6.4e-44 | yrzL | S | Belongs to the UPF0297 family | ||
FEAFEJEJ_00469 | 1.5e-74 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
FEAFEJEJ_00470 | 1.6e-51 | yrzB | S | Belongs to the UPF0473 family | ||
FEAFEJEJ_00471 | 1.2e-39 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
FEAFEJEJ_00472 | 6.4e-88 | cvpA | S | Colicin V production protein | ||
FEAFEJEJ_00473 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
FEAFEJEJ_00474 | 2.7e-54 | trxA | O | Belongs to the thioredoxin family | ||
FEAFEJEJ_00475 | 7.2e-92 | yslB | S | Protein of unknown function (DUF2507) | ||
FEAFEJEJ_00476 | 2.2e-148 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
FEAFEJEJ_00477 | 9.6e-109 | 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 | |
FEAFEJEJ_00478 | 1.9e-100 | S | Phosphoesterase | |||
FEAFEJEJ_00479 | 4.6e-85 | ykuL | S | (CBS) domain | ||
FEAFEJEJ_00480 | 4.7e-48 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
FEAFEJEJ_00481 | 1.8e-251 | U | Major Facilitator Superfamily | |||
FEAFEJEJ_00482 | 4.1e-156 | ykuT | M | mechanosensitive ion channel | ||
FEAFEJEJ_00483 | 6.9e-34 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
FEAFEJEJ_00484 | 9.5e-43 | |||||
FEAFEJEJ_00485 | 2.7e-210 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
FEAFEJEJ_00486 | 1.6e-180 | ccpA | K | catabolite control protein A | ||
FEAFEJEJ_00487 | 2.7e-133 | |||||
FEAFEJEJ_00488 | 5.7e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
FEAFEJEJ_00489 | 2.3e-257 | glnPH2 | P | ABC transporter permease | ||
FEAFEJEJ_00490 | 2.6e-132 | yebC | K | Transcriptional regulatory protein | ||
FEAFEJEJ_00491 | 1.2e-172 | comGA | NU | Type II IV secretion system protein | ||
FEAFEJEJ_00492 | 3.1e-170 | comGB | NU | type II secretion system | ||
FEAFEJEJ_00493 | 7.6e-49 | comGC | U | competence protein ComGC | ||
FEAFEJEJ_00494 | 3.4e-82 | |||||
FEAFEJEJ_00496 | 1.1e-74 | |||||
FEAFEJEJ_00497 | 1.5e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
FEAFEJEJ_00498 | 1.1e-220 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
FEAFEJEJ_00499 | 2e-258 | cycA | E | Amino acid permease | ||
FEAFEJEJ_00500 | 8.7e-156 | yeaE | S | Aldo keto | ||
FEAFEJEJ_00501 | 5.3e-115 | S | Calcineurin-like phosphoesterase | |||
FEAFEJEJ_00502 | 2.3e-270 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
FEAFEJEJ_00503 | 1.1e-86 | yutD | S | Protein of unknown function (DUF1027) | ||
FEAFEJEJ_00504 | 1.5e-146 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
FEAFEJEJ_00505 | 7.7e-117 | S | Protein of unknown function (DUF1461) | |||
FEAFEJEJ_00506 | 6.9e-89 | S | WxL domain surface cell wall-binding | |||
FEAFEJEJ_00507 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
FEAFEJEJ_00508 | 2.1e-129 | M | domain protein | |||
FEAFEJEJ_00509 | 3.6e-244 | yfnA | E | Amino Acid | ||
FEAFEJEJ_00510 | 3.6e-143 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
FEAFEJEJ_00511 | 2.9e-122 | dedA | S | SNARE-like domain protein | ||
FEAFEJEJ_00512 | 6.1e-88 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
FEAFEJEJ_00513 | 3.5e-111 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
FEAFEJEJ_00514 | 5.2e-71 | yugI | 5.3.1.9 | J | general stress protein | |
FEAFEJEJ_00523 | 1.2e-07 | |||||
FEAFEJEJ_00533 | 7.3e-233 | N | Uncharacterized conserved protein (DUF2075) | |||
FEAFEJEJ_00534 | 1.8e-92 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
FEAFEJEJ_00535 | 3.2e-138 | yhfI | S | Metallo-beta-lactamase superfamily | ||
FEAFEJEJ_00536 | 2.2e-193 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00537 | 1e-69 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
FEAFEJEJ_00538 | 1.7e-120 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
FEAFEJEJ_00539 | 9.5e-104 | T | EAL domain | |||
FEAFEJEJ_00540 | 2.6e-91 | |||||
FEAFEJEJ_00541 | 3.1e-234 | pgaC | GT2 | M | Glycosyl transferase | |
FEAFEJEJ_00543 | 3.7e-102 | ytqB | J | Putative rRNA methylase | ||
FEAFEJEJ_00544 | 3.9e-116 | pgpB1 | 3.6.1.27 | I | Acid phosphatase homologues | |
FEAFEJEJ_00545 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
FEAFEJEJ_00546 | 5.2e-119 | P | ABC-type multidrug transport system ATPase component | |||
FEAFEJEJ_00547 | 4.8e-145 | S | NADPH-dependent FMN reductase | |||
FEAFEJEJ_00548 | 4.4e-52 | |||||
FEAFEJEJ_00549 | 8.8e-298 | ytgP | S | Polysaccharide biosynthesis protein | ||
FEAFEJEJ_00550 | 4.9e-125 | rluB | 5.4.99.19, 5.4.99.20, 5.4.99.21, 5.4.99.22 | J | pseudouridine synthase activity | |
FEAFEJEJ_00551 | 1.3e-148 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
FEAFEJEJ_00552 | 2.4e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
FEAFEJEJ_00553 | 8.2e-85 | uspA | T | Belongs to the universal stress protein A family | ||
FEAFEJEJ_00554 | 1.2e-202 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
FEAFEJEJ_00555 | 7.2e-245 | cycA | E | Amino acid permease | ||
FEAFEJEJ_00556 | 2e-55 | ytzB | S | Small secreted protein | ||
FEAFEJEJ_00557 | 4e-56 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
FEAFEJEJ_00558 | 1.4e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
FEAFEJEJ_00559 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
FEAFEJEJ_00560 | 1.6e-257 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
FEAFEJEJ_00561 | 1.6e-230 | L | Transposase | |||
FEAFEJEJ_00562 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_00563 | 1.2e-80 | pnuC | H | nicotinamide mononucleotide transporter | ||
FEAFEJEJ_00564 | 1.9e-37 | pnuC | H | nicotinamide mononucleotide transporter | ||
FEAFEJEJ_00565 | 7.1e-119 | ybhL | S | Belongs to the BI1 family | ||
FEAFEJEJ_00566 | 1.9e-237 | F | Permease | |||
FEAFEJEJ_00567 | 9e-264 | guaD | 3.5.4.3 | F | Amidohydrolase family | |
FEAFEJEJ_00568 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
FEAFEJEJ_00569 | 2.3e-164 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
FEAFEJEJ_00570 | 2.8e-111 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
FEAFEJEJ_00571 | 7.8e-88 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
FEAFEJEJ_00572 | 4.9e-249 | dnaB | L | replication initiation and membrane attachment | ||
FEAFEJEJ_00573 | 1.3e-165 | dnaI | L | Primosomal protein DnaI | ||
FEAFEJEJ_00574 | 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) | |
FEAFEJEJ_00575 | 4.4e-79 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
FEAFEJEJ_00576 | 5.1e-27 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
FEAFEJEJ_00577 | 3.7e-55 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
FEAFEJEJ_00578 | 3.2e-103 | yqeG | S | HAD phosphatase, family IIIA | ||
FEAFEJEJ_00579 | 8.5e-223 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
FEAFEJEJ_00580 | 1.3e-48 | yhbY | J | RNA-binding protein | ||
FEAFEJEJ_00581 | 5.9e-117 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
FEAFEJEJ_00582 | 7.3e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
FEAFEJEJ_00583 | 5.4e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
FEAFEJEJ_00584 | 5.9e-140 | yqeM | Q | Methyltransferase | ||
FEAFEJEJ_00585 | 2.9e-215 | ylbM | S | Belongs to the UPF0348 family | ||
FEAFEJEJ_00586 | 8.6e-96 | yceD | S | Uncharacterized ACR, COG1399 | ||
FEAFEJEJ_00587 | 6.9e-29 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
FEAFEJEJ_00588 | 4.9e-148 | 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | ||
FEAFEJEJ_00589 | 7.4e-52 | K | Transcriptional regulator, ArsR family | |||
FEAFEJEJ_00590 | 1.5e-115 | zmp3 | O | Zinc-dependent metalloprotease | ||
FEAFEJEJ_00591 | 1.9e-194 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
FEAFEJEJ_00592 | 2.8e-120 | K | response regulator | |||
FEAFEJEJ_00593 | 1.1e-292 | arlS | 2.7.13.3 | T | Histidine kinase | |
FEAFEJEJ_00594 | 9.2e-71 | S | Protein of unknown function (DUF1093) | |||
FEAFEJEJ_00595 | 8.4e-133 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
FEAFEJEJ_00596 | 8.4e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
FEAFEJEJ_00597 | 9.4e-141 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
FEAFEJEJ_00598 | 4e-92 | 2.7.7.19, 2.7.7.72 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
FEAFEJEJ_00599 | 3.9e-68 | yodB | K | Transcriptional regulator, HxlR family | ||
FEAFEJEJ_00600 | 5.8e-202 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
FEAFEJEJ_00601 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
FEAFEJEJ_00602 | 5e-207 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
FEAFEJEJ_00603 | 1e-119 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
FEAFEJEJ_00604 | 6.3e-71 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
FEAFEJEJ_00605 | 1.7e-56 | yneR | S | Belongs to the HesB IscA family | ||
FEAFEJEJ_00606 | 0.0 | S | membrane | |||
FEAFEJEJ_00607 | 6.5e-28 | CP_0775 | S | Domain of unknown function (DUF378) | ||
FEAFEJEJ_00608 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
FEAFEJEJ_00609 | 2.5e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
FEAFEJEJ_00610 | 7e-98 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
FEAFEJEJ_00611 | 4e-119 | gluP | 3.4.21.105 | S | Peptidase, S54 family | |
FEAFEJEJ_00612 | 9.3e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
FEAFEJEJ_00613 | 8.9e-181 | glk | 2.7.1.2 | G | Glucokinase | |
FEAFEJEJ_00614 | 2.1e-70 | yqhL | P | Rhodanese-like protein | ||
FEAFEJEJ_00615 | 3.1e-23 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
FEAFEJEJ_00616 | 7e-141 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
FEAFEJEJ_00617 | 1.2e-171 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
FEAFEJEJ_00618 | 2.8e-64 | glnR | K | Transcriptional regulator | ||
FEAFEJEJ_00619 | 3.7e-262 | glnA | 6.3.1.2 | E | glutamine synthetase | |
FEAFEJEJ_00620 | 3.1e-156 | |||||
FEAFEJEJ_00621 | 1.8e-178 | |||||
FEAFEJEJ_00622 | 2.2e-96 | dut | S | Protein conserved in bacteria | ||
FEAFEJEJ_00623 | 4.1e-95 | K | Transcriptional regulator | |||
FEAFEJEJ_00624 | 3.4e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
FEAFEJEJ_00625 | 2.2e-57 | ysxB | J | Cysteine protease Prp | ||
FEAFEJEJ_00626 | 1.6e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
FEAFEJEJ_00627 | 2.8e-191 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
FEAFEJEJ_00628 | 1.3e-99 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
FEAFEJEJ_00629 | 4.8e-73 | yqhY | S | Asp23 family, cell envelope-related function | ||
FEAFEJEJ_00630 | 7.2e-74 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
FEAFEJEJ_00631 | 6.2e-157 | 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 | |
FEAFEJEJ_00632 | 4.7e-244 | 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 | |
FEAFEJEJ_00633 | 2.9e-35 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
FEAFEJEJ_00634 | 7.6e-166 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
FEAFEJEJ_00635 | 2.6e-149 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
FEAFEJEJ_00636 | 3.7e-76 | argR | K | Regulates arginine biosynthesis genes | ||
FEAFEJEJ_00637 | 8e-310 | recN | L | May be involved in recombinational repair of damaged DNA | ||
FEAFEJEJ_00639 | 3.4e-52 | |||||
FEAFEJEJ_00640 | 3.3e-104 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
FEAFEJEJ_00641 | 4.9e-31 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
FEAFEJEJ_00642 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_00643 | 3.7e-216 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
FEAFEJEJ_00644 | 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 | ||
FEAFEJEJ_00645 | 1.5e-172 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
FEAFEJEJ_00646 | 1.6e-228 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
FEAFEJEJ_00647 | 6.5e-131 | stp | 3.1.3.16 | T | phosphatase | |
FEAFEJEJ_00648 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
FEAFEJEJ_00649 | 1.2e-168 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
FEAFEJEJ_00650 | 1.1e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
FEAFEJEJ_00651 | 4.7e-128 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
FEAFEJEJ_00652 | 4.9e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
FEAFEJEJ_00653 | 5.2e-57 | asp | S | Asp23 family, cell envelope-related function | ||
FEAFEJEJ_00654 | 0.0 | yloV | S | DAK2 domain fusion protein YloV | ||
FEAFEJEJ_00655 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
FEAFEJEJ_00656 | 4.7e-188 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
FEAFEJEJ_00657 | 6.4e-38 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
FEAFEJEJ_00658 | 2.8e-128 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
FEAFEJEJ_00659 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
FEAFEJEJ_00660 | 1e-172 | 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) | ||
FEAFEJEJ_00661 | 2.9e-57 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
FEAFEJEJ_00662 | 1.1e-206 | 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 | |
FEAFEJEJ_00663 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
FEAFEJEJ_00664 | 4.3e-214 | 3.1.3.1 | S | associated with various cellular activities | ||
FEAFEJEJ_00665 | 5e-251 | S | Putative metallopeptidase domain | |||
FEAFEJEJ_00666 | 2.1e-48 | |||||
FEAFEJEJ_00667 | 3.8e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
FEAFEJEJ_00668 | 1.9e-40 | ylqC | S | Belongs to the UPF0109 family | ||
FEAFEJEJ_00669 | 4.1e-92 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
FEAFEJEJ_00670 | 2.4e-144 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
FEAFEJEJ_00671 | 2.7e-58 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
FEAFEJEJ_00672 | 2.3e-75 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
FEAFEJEJ_00673 | 2.1e-79 | marR | K | Transcriptional regulator | ||
FEAFEJEJ_00674 | 1.7e-182 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
FEAFEJEJ_00675 | 2e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
FEAFEJEJ_00676 | 2.2e-165 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
FEAFEJEJ_00677 | 3.2e-122 | IQ | reductase | |||
FEAFEJEJ_00678 | 1.2e-227 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
FEAFEJEJ_00679 | 3e-72 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
FEAFEJEJ_00680 | 3.8e-72 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
FEAFEJEJ_00681 | 1.2e-266 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
FEAFEJEJ_00682 | 2.1e-154 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
FEAFEJEJ_00683 | 1.7e-142 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
FEAFEJEJ_00684 | 5.3e-128 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
FEAFEJEJ_00685 | 8.4e-145 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
FEAFEJEJ_00686 | 2.2e-85 | bioY | S | BioY family | ||
FEAFEJEJ_00687 | 1.1e-50 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
FEAFEJEJ_00688 | 2e-91 | entB | 3.5.1.19 | Q | Isochorismatase family | |
FEAFEJEJ_00689 | 6.1e-79 | S | Protein of unknown function (DUF3021) | |||
FEAFEJEJ_00690 | 8.7e-75 | K | LytTr DNA-binding domain | |||
FEAFEJEJ_00691 | 2.4e-50 | N | PFAM Uncharacterised protein family UPF0150 | |||
FEAFEJEJ_00692 | 1.8e-91 | ydeA | 3.5.1.124 | S | DJ-1/PfpI family | |
FEAFEJEJ_00693 | 3.3e-32 | yyaQ | S | YjbR | ||
FEAFEJEJ_00694 | 1.4e-175 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00695 | 6.7e-31 | adhR | K | MerR, DNA binding | ||
FEAFEJEJ_00696 | 3.9e-187 | C | Aldo/keto reductase family | |||
FEAFEJEJ_00697 | 1.8e-195 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
FEAFEJEJ_00698 | 7.8e-67 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
FEAFEJEJ_00699 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_00700 | 5.2e-220 | katA | 1.11.1.6 | C | Belongs to the catalase family | |
FEAFEJEJ_00701 | 1.8e-98 | rimL | J | Acetyltransferase (GNAT) domain | ||
FEAFEJEJ_00702 | 6.2e-70 | |||||
FEAFEJEJ_00703 | 1.5e-10 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_00704 | 3.3e-49 | K | Helix-turn-helix | |||
FEAFEJEJ_00705 | 5.5e-76 | K | Helix-turn-helix | |||
FEAFEJEJ_00706 | 7.7e-280 | yjeM | E | Amino Acid | ||
FEAFEJEJ_00707 | 3.5e-274 | pipD | E | Dipeptidase | ||
FEAFEJEJ_00708 | 4.7e-155 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
FEAFEJEJ_00709 | 1.4e-26 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
FEAFEJEJ_00710 | 9.9e-296 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
FEAFEJEJ_00711 | 5.3e-189 | L | Helix-turn-helix domain | |||
FEAFEJEJ_00713 | 5.3e-56 | S | Protein of unknown function (DUF2975) | |||
FEAFEJEJ_00714 | 3.7e-28 | yozG | K | Transcriptional regulator | ||
FEAFEJEJ_00715 | 8.8e-202 | |||||
FEAFEJEJ_00716 | 4.1e-99 | |||||
FEAFEJEJ_00717 | 5.6e-203 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
FEAFEJEJ_00718 | 6.3e-60 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
FEAFEJEJ_00719 | 8.5e-114 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
FEAFEJEJ_00720 | 0.0 | yhcA | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00721 | 1.7e-102 | bm3R1 | K | Psort location Cytoplasmic, score | ||
FEAFEJEJ_00722 | 4.5e-70 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
FEAFEJEJ_00723 | 1.7e-38 | S | Mor transcription activator family | |||
FEAFEJEJ_00724 | 2.9e-41 | S | Mor transcription activator family | |||
FEAFEJEJ_00725 | 5.8e-126 | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
FEAFEJEJ_00726 | 1.4e-19 | S | Mor transcription activator family | |||
FEAFEJEJ_00727 | 8.6e-128 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
FEAFEJEJ_00728 | 3.6e-192 | ybhR | V | ABC transporter | ||
FEAFEJEJ_00729 | 1.3e-111 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_00730 | 4e-177 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
FEAFEJEJ_00731 | 5.4e-59 | yqkB | S | Belongs to the HesB IscA family | ||
FEAFEJEJ_00732 | 2e-162 | yjcE | P | Sodium proton antiporter | ||
FEAFEJEJ_00733 | 3.9e-19 | yjcE | P | Sodium proton antiporter | ||
FEAFEJEJ_00734 | 1.2e-33 | yeaN | P | Major Facilitator Superfamily | ||
FEAFEJEJ_00735 | 0.0 | kup | P | Transport of potassium into the cell | ||
FEAFEJEJ_00736 | 3.9e-184 | C | Zinc-binding dehydrogenase | |||
FEAFEJEJ_00737 | 3.1e-18 | 1.1.1.219 | GM | Male sterility protein | ||
FEAFEJEJ_00738 | 2.6e-73 | 1.1.1.219 | GM | Male sterility protein | ||
FEAFEJEJ_00739 | 3.8e-78 | K | helix_turn_helix, mercury resistance | |||
FEAFEJEJ_00740 | 7.2e-66 | K | MarR family | |||
FEAFEJEJ_00741 | 1.3e-48 | S | Uncharacterized protein conserved in bacteria (DUF2316) | |||
FEAFEJEJ_00742 | 1e-198 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
FEAFEJEJ_00743 | 1.2e-39 | K | Transcriptional regulator | |||
FEAFEJEJ_00744 | 7.4e-30 | K | Transcriptional regulator | |||
FEAFEJEJ_00745 | 2.6e-163 | akr5f | 1.1.1.346 | S | reductase | |
FEAFEJEJ_00746 | 4.2e-166 | S | Oxidoreductase, aldo keto reductase family protein | |||
FEAFEJEJ_00747 | 1e-81 | |||||
FEAFEJEJ_00748 | 3.9e-215 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
FEAFEJEJ_00749 | 3e-153 | yitU | 3.1.3.104 | S | hydrolase | |
FEAFEJEJ_00750 | 1.4e-269 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
FEAFEJEJ_00751 | 1.9e-189 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
FEAFEJEJ_00752 | 6.4e-204 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
FEAFEJEJ_00753 | 1.6e-174 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
FEAFEJEJ_00754 | 2.5e-172 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
FEAFEJEJ_00755 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
FEAFEJEJ_00756 | 2.6e-83 | ypmB | S | Protein conserved in bacteria | ||
FEAFEJEJ_00757 | 9.1e-212 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
FEAFEJEJ_00758 | 5.5e-124 | dnaD | L | Replication initiation and membrane attachment | ||
FEAFEJEJ_00759 | 1.1e-87 | yetL | K | helix_turn_helix multiple antibiotic resistance protein | ||
FEAFEJEJ_00760 | 3.5e-61 | P | Rhodanese Homology Domain | |||
FEAFEJEJ_00761 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
FEAFEJEJ_00762 | 1.4e-112 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
FEAFEJEJ_00763 | 5e-107 | ypsA | S | Belongs to the UPF0398 family | ||
FEAFEJEJ_00764 | 6.4e-28 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
FEAFEJEJ_00766 | 3.6e-221 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
FEAFEJEJ_00767 | 2.3e-68 | FG | Scavenger mRNA decapping enzyme C-term binding | |||
FEAFEJEJ_00768 | 5.3e-248 | amtB | P | ammonium transporter | ||
FEAFEJEJ_00769 | 4.8e-28 | |||||
FEAFEJEJ_00770 | 9.7e-84 | mutT | 3.6.1.55 | F | Belongs to the Nudix hydrolase family | |
FEAFEJEJ_00771 | 4e-54 | |||||
FEAFEJEJ_00772 | 9.7e-126 | S | CAAX protease self-immunity | |||
FEAFEJEJ_00773 | 3.4e-86 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_00774 | 1.6e-111 | XK27_02070 | S | Nitroreductase family | ||
FEAFEJEJ_00775 | 9.9e-208 | yurR | 1.4.5.1 | E | FAD dependent oxidoreductase | |
FEAFEJEJ_00776 | 2.9e-64 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
FEAFEJEJ_00777 | 9.3e-56 | esbA | S | Family of unknown function (DUF5322) | ||
FEAFEJEJ_00778 | 3.5e-302 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
FEAFEJEJ_00779 | 5.7e-81 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
FEAFEJEJ_00780 | 5.5e-172 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
FEAFEJEJ_00781 | 6.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
FEAFEJEJ_00782 | 1.5e-205 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
FEAFEJEJ_00783 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
FEAFEJEJ_00784 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
FEAFEJEJ_00785 | 6.3e-70 | K | Transcriptional regulator | |||
FEAFEJEJ_00786 | 1.7e-198 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
FEAFEJEJ_00787 | 8.4e-232 | yxiO | S | Vacuole effluxer Atg22 like | ||
FEAFEJEJ_00788 | 7.8e-160 | degV | S | EDD domain protein, DegV family | ||
FEAFEJEJ_00789 | 4.1e-87 | folT | S | ECF transporter, substrate-specific component | ||
FEAFEJEJ_00790 | 5.1e-75 | gtcA | S | Teichoic acid glycosylation protein | ||
FEAFEJEJ_00791 | 3e-87 | ysaA | V | VanZ like family | ||
FEAFEJEJ_00792 | 6.9e-92 | V | VanZ like family | |||
FEAFEJEJ_00793 | 8.5e-119 | 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 | |
FEAFEJEJ_00794 | 2.7e-146 | mta | K | helix_turn_helix, mercury resistance | ||
FEAFEJEJ_00795 | 3.1e-178 | C | Zinc-binding dehydrogenase | |||
FEAFEJEJ_00796 | 3.3e-149 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
FEAFEJEJ_00797 | 3.6e-131 | Q | Methyltransferase domain | |||
FEAFEJEJ_00798 | 1.1e-164 | |||||
FEAFEJEJ_00799 | 1.4e-175 | L | Integrase core domain | |||
FEAFEJEJ_00800 | 2.6e-228 | L | Transposase | |||
FEAFEJEJ_00801 | 1.4e-161 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_00802 | 6.7e-32 | |||||
FEAFEJEJ_00803 | 1.6e-199 | xerS | L | Belongs to the 'phage' integrase family | ||
FEAFEJEJ_00804 | 4.6e-76 | 3.6.1.55 | F | NUDIX domain | ||
FEAFEJEJ_00805 | 2.8e-99 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
FEAFEJEJ_00806 | 1.3e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
FEAFEJEJ_00807 | 4.2e-101 | zmp1 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
FEAFEJEJ_00808 | 3.7e-168 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
FEAFEJEJ_00809 | 1.6e-182 | K | Transcriptional regulator | |||
FEAFEJEJ_00810 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
FEAFEJEJ_00811 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
FEAFEJEJ_00812 | 1.2e-98 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
FEAFEJEJ_00813 | 1.9e-169 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
FEAFEJEJ_00814 | 1.8e-262 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
FEAFEJEJ_00815 | 1.8e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
FEAFEJEJ_00816 | 5.8e-177 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
FEAFEJEJ_00817 | 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 | |
FEAFEJEJ_00818 | 3.8e-162 | dprA | LU | DNA protecting protein DprA | ||
FEAFEJEJ_00819 | 3.3e-136 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
FEAFEJEJ_00820 | 1.5e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
FEAFEJEJ_00822 | 4.1e-74 | abiGI | K | Psort location Cytoplasmic, score | ||
FEAFEJEJ_00823 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_00826 | 5.7e-129 | |||||
FEAFEJEJ_00827 | 5.8e-35 | yozE | S | Belongs to the UPF0346 family | ||
FEAFEJEJ_00828 | 6.5e-105 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
FEAFEJEJ_00829 | 4.5e-166 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
FEAFEJEJ_00830 | 2.3e-148 | DegV | S | EDD domain protein, DegV family | ||
FEAFEJEJ_00831 | 4.8e-114 | hlyIII | S | protein, hemolysin III | ||
FEAFEJEJ_00832 | 5e-240 | L | Transposase | |||
FEAFEJEJ_00833 | 7.4e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
FEAFEJEJ_00834 | 2.8e-187 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
FEAFEJEJ_00835 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_00836 | 1.7e-218 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
FEAFEJEJ_00837 | 1.3e-171 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
FEAFEJEJ_00838 | 2.9e-232 | S | Tetratricopeptide repeat protein | |||
FEAFEJEJ_00839 | 1.5e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
FEAFEJEJ_00840 | 6.7e-248 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
FEAFEJEJ_00841 | 1.1e-210 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
FEAFEJEJ_00842 | 6.4e-117 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
FEAFEJEJ_00843 | 8e-26 | M | Lysin motif | |||
FEAFEJEJ_00844 | 3.7e-252 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
FEAFEJEJ_00845 | 4.1e-184 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
FEAFEJEJ_00846 | 6.5e-94 | 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 | |||
FEAFEJEJ_00847 | 2.7e-129 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
FEAFEJEJ_00848 | 3e-102 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
FEAFEJEJ_00849 | 7.4e-133 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
FEAFEJEJ_00850 | 3.1e-71 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
FEAFEJEJ_00851 | 9.8e-166 | xerD | D | recombinase XerD | ||
FEAFEJEJ_00852 | 9.3e-169 | cvfB | S | S1 domain | ||
FEAFEJEJ_00853 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
FEAFEJEJ_00854 | 7.3e-127 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
FEAFEJEJ_00855 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
FEAFEJEJ_00856 | 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 | ||
FEAFEJEJ_00857 | 2.5e-236 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
FEAFEJEJ_00858 | 3.1e-155 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
FEAFEJEJ_00859 | 2.3e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
FEAFEJEJ_00860 | 0.0 | ydgH | S | MMPL family | ||
FEAFEJEJ_00861 | 1.6e-88 | K | Transcriptional regulator | |||
FEAFEJEJ_00862 | 4.6e-197 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
FEAFEJEJ_00863 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
FEAFEJEJ_00864 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
FEAFEJEJ_00865 | 1.5e-177 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
FEAFEJEJ_00866 | 8.6e-150 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
FEAFEJEJ_00867 | 1.5e-169 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
FEAFEJEJ_00868 | 7.6e-62 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
FEAFEJEJ_00869 | 8.5e-79 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
FEAFEJEJ_00870 | 1.6e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
FEAFEJEJ_00871 | 7e-72 | yqeY | S | YqeY-like protein | ||
FEAFEJEJ_00872 | 3.4e-67 | hxlR | K | Transcriptional regulator, HxlR family | ||
FEAFEJEJ_00873 | 2e-194 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
FEAFEJEJ_00874 | 1.3e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
FEAFEJEJ_00875 | 1.3e-151 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
FEAFEJEJ_00876 | 2.9e-173 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
FEAFEJEJ_00877 | 1.8e-242 | tagF1 | 2.7.8.12, 2.7.8.45 | M | glycerophosphotransferase | |
FEAFEJEJ_00878 | 8e-151 | tagG | U | Transport permease protein | ||
FEAFEJEJ_00879 | 1.5e-190 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
FEAFEJEJ_00880 | 1.1e-161 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
FEAFEJEJ_00881 | 2.8e-96 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
FEAFEJEJ_00882 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
FEAFEJEJ_00883 | 3.3e-247 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
FEAFEJEJ_00884 | 6.1e-99 | |||||
FEAFEJEJ_00885 | 5.8e-160 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
FEAFEJEJ_00886 | 3.5e-165 | yniA | G | Fructosamine kinase | ||
FEAFEJEJ_00887 | 5.1e-116 | 3.1.3.18 | S | HAD-hyrolase-like | ||
FEAFEJEJ_00888 | 1.1e-75 | 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 | ||
FEAFEJEJ_00889 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
FEAFEJEJ_00890 | 2.7e-60 | |||||
FEAFEJEJ_00891 | 3.4e-135 | 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 | |
FEAFEJEJ_00892 | 9.7e-180 | prmA | J | Ribosomal protein L11 methyltransferase | ||
FEAFEJEJ_00893 | 4.7e-54 | |||||
FEAFEJEJ_00894 | 9.1e-28 | 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 | ||
FEAFEJEJ_00895 | 1.8e-62 | |||||
FEAFEJEJ_00897 | 3.3e-42 | |||||
FEAFEJEJ_00899 | 4.8e-213 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
FEAFEJEJ_00901 | 3.5e-76 | L | Transposase DDE domain | |||
FEAFEJEJ_00902 | 2.7e-30 | L | Putative transposase of IS4/5 family (DUF4096) | |||
FEAFEJEJ_00903 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_00904 | 5.7e-09 | 2.7.7.65 | T | diguanylate cyclase | ||
FEAFEJEJ_00905 | 3.7e-176 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00906 | 6.6e-173 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00907 | 8.1e-09 | |||||
FEAFEJEJ_00908 | 1e-53 | asp2 | S | Asp23 family, cell envelope-related function | ||
FEAFEJEJ_00909 | 9.2e-66 | asp | S | Asp23 family, cell envelope-related function | ||
FEAFEJEJ_00910 | 5.5e-71 | |||||
FEAFEJEJ_00911 | 3.7e-25 | S | Transglycosylase associated protein | |||
FEAFEJEJ_00912 | 9.6e-197 | M | Glycosyl hydrolases family 25 | |||
FEAFEJEJ_00915 | 1.6e-29 | |||||
FEAFEJEJ_00919 | 7.8e-12 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
FEAFEJEJ_00920 | 6.7e-08 | |||||
FEAFEJEJ_00921 | 4.9e-67 | Z012_12235 | S | Baseplate J-like protein | ||
FEAFEJEJ_00923 | 1.1e-11 | |||||
FEAFEJEJ_00924 | 2.1e-57 | |||||
FEAFEJEJ_00925 | 3.9e-09 | |||||
FEAFEJEJ_00926 | 3.3e-26 | M | LysM domain | |||
FEAFEJEJ_00927 | 1e-36 | dnaG | D | tape measure | ||
FEAFEJEJ_00928 | 3.6e-116 | S | peptidoglycan catabolic process | |||
FEAFEJEJ_00930 | 2.1e-10 | |||||
FEAFEJEJ_00931 | 6.1e-08 | S | Protein of unknown function (DUF3383) | |||
FEAFEJEJ_00934 | 7e-43 | |||||
FEAFEJEJ_00936 | 7e-99 | gpG | ||||
FEAFEJEJ_00938 | 5.1e-32 | S | head morphogenesis protein, SPP1 gp7 family | |||
FEAFEJEJ_00939 | 4.8e-145 | S | Phage portal protein, SPP1 Gp6-like | |||
FEAFEJEJ_00943 | 2.1e-186 | S | TIGRFAM Phage | |||
FEAFEJEJ_00944 | 2.4e-59 | L | transposase activity | |||
FEAFEJEJ_00946 | 1.5e-188 | L | Helix-turn-helix domain | |||
FEAFEJEJ_00947 | 1.4e-175 | L | Integrase core domain | |||
FEAFEJEJ_00951 | 1.5e-53 | |||||
FEAFEJEJ_00953 | 2.4e-43 | arpU | S | Phage transcriptional regulator, ArpU family | ||
FEAFEJEJ_00954 | 4.5e-33 | S | YopX protein | |||
FEAFEJEJ_00955 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00957 | 4e-42 | S | Endodeoxyribonuclease RusA | |||
FEAFEJEJ_00958 | 8.6e-56 | K | AntA/AntB antirepressor | |||
FEAFEJEJ_00959 | 1.6e-18 | L | Replication initiation and membrane attachment | |||
FEAFEJEJ_00960 | 1.1e-83 | pi112 | 3.6.4.12 | L | PDDEXK-like domain of unknown function (DUF3799) | |
FEAFEJEJ_00961 | 5e-68 | recT | L | RecT family | ||
FEAFEJEJ_00966 | 2.1e-07 | |||||
FEAFEJEJ_00969 | 1.1e-12 | sinR | K | Helix-turn-helix XRE-family like proteins | ||
FEAFEJEJ_00970 | 6.6e-173 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_00971 | 1.8e-33 | yvaO | K | Helix-turn-helix XRE-family like proteins | ||
FEAFEJEJ_00972 | 2.7e-46 | E | IrrE N-terminal-like domain | |||
FEAFEJEJ_00975 | 3.3e-135 | 3.6.4.12 | L | Belongs to the 'phage' integrase family | ||
FEAFEJEJ_00976 | 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 | ||
FEAFEJEJ_00977 | 3.2e-250 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
FEAFEJEJ_00978 | 5.2e-34 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
FEAFEJEJ_00979 | 3.2e-236 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
FEAFEJEJ_00980 | 1.3e-298 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
FEAFEJEJ_00981 | 1.7e-17 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
FEAFEJEJ_00982 | 1.3e-178 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
FEAFEJEJ_00983 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
FEAFEJEJ_00984 | 1.8e-83 | 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 | ||
FEAFEJEJ_00985 | 7.8e-191 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
FEAFEJEJ_00986 | 4.3e-180 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
FEAFEJEJ_00987 | 6.7e-170 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
FEAFEJEJ_00988 | 9.4e-56 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
FEAFEJEJ_00989 | 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 | ||
FEAFEJEJ_00990 | 1.4e-44 | ylxQ | J | ribosomal protein | ||
FEAFEJEJ_00991 | 2.3e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
FEAFEJEJ_00992 | 1.2e-190 | nusA | K | Participates in both transcription termination and antitermination | ||
FEAFEJEJ_00993 | 1.8e-81 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
FEAFEJEJ_00994 | 1.4e-38 | |||||
FEAFEJEJ_00995 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
FEAFEJEJ_00996 | 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 | |
FEAFEJEJ_00997 | 5.9e-233 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
FEAFEJEJ_00998 | 5.3e-139 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
FEAFEJEJ_00999 | 1.1e-147 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
FEAFEJEJ_01000 | 3.2e-74 | |||||
FEAFEJEJ_01001 | 2.4e-85 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
FEAFEJEJ_01002 | 1.7e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
FEAFEJEJ_01003 | 1.9e-153 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
FEAFEJEJ_01004 | 3.8e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
FEAFEJEJ_01005 | 2.2e-136 | S | Haloacid dehalogenase-like hydrolase | |||
FEAFEJEJ_01006 | 4.7e-185 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
FEAFEJEJ_01007 | 2.2e-44 | yazA | L | GIY-YIG catalytic domain protein | ||
FEAFEJEJ_01008 | 2.1e-137 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
FEAFEJEJ_01009 | 4e-121 | plsC | 2.3.1.51 | I | Acyltransferase | |
FEAFEJEJ_01010 | 0.0 | mdlB | V | ABC transporter | ||
FEAFEJEJ_01011 | 9.9e-287 | mdlA | V | ABC transporter | ||
FEAFEJEJ_01012 | 1.6e-32 | yneF | S | Uncharacterised protein family (UPF0154) | ||
FEAFEJEJ_01013 | 1.8e-37 | ynzC | S | UPF0291 protein | ||
FEAFEJEJ_01014 | 3.1e-110 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
FEAFEJEJ_01015 | 7.9e-76 | F | nucleoside 2-deoxyribosyltransferase | |||
FEAFEJEJ_01016 | 1.6e-79 | |||||
FEAFEJEJ_01017 | 6.5e-218 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
FEAFEJEJ_01018 | 2.4e-164 | S | Polyphosphate nucleotide phosphotransferase, PPK2 family | |||
FEAFEJEJ_01019 | 5.3e-124 | G | phosphoglycerate mutase | |||
FEAFEJEJ_01020 | 7.7e-25 | KT | PspC domain | |||
FEAFEJEJ_01021 | 4.6e-82 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
FEAFEJEJ_01025 | 1.3e-69 | S | MTH538 TIR-like domain (DUF1863) | |||
FEAFEJEJ_01026 | 2.2e-165 | yegS | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain | |
FEAFEJEJ_01027 | 1.3e-74 | |||||
FEAFEJEJ_01028 | 1.9e-161 | L | An automated process has identified a potential problem with this gene model | |||
FEAFEJEJ_01030 | 1.1e-77 | T | Universal stress protein family | |||
FEAFEJEJ_01031 | 3.2e-92 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
FEAFEJEJ_01032 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
FEAFEJEJ_01033 | 4e-55 | yrvD | S | Pfam:DUF1049 | ||
FEAFEJEJ_01034 | 5.7e-180 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
FEAFEJEJ_01035 | 3.8e-28 | |||||
FEAFEJEJ_01036 | 6.2e-105 | |||||
FEAFEJEJ_01037 | 1.6e-246 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
FEAFEJEJ_01038 | 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 | ||
FEAFEJEJ_01039 | 1.1e-15 | |||||
FEAFEJEJ_01040 | 3.2e-52 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
FEAFEJEJ_01041 | 6.6e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
FEAFEJEJ_01042 | 6.9e-234 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
FEAFEJEJ_01043 | 2.2e-222 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
FEAFEJEJ_01044 | 1.9e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
FEAFEJEJ_01045 | 3.2e-167 | S | Tetratricopeptide repeat | |||
FEAFEJEJ_01046 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
FEAFEJEJ_01047 | 1.3e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
FEAFEJEJ_01048 | 2.1e-33 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
FEAFEJEJ_01049 | 1.4e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
FEAFEJEJ_01050 | 0.0 | comEC | S | Competence protein ComEC | ||
FEAFEJEJ_01051 | 8.8e-89 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
FEAFEJEJ_01052 | 9.7e-121 | comEA | L | Competence protein ComEA | ||
FEAFEJEJ_01053 | 3e-198 | ylbL | T | Belongs to the peptidase S16 family | ||
FEAFEJEJ_01054 | 7.3e-83 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
FEAFEJEJ_01055 | 2.2e-99 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
FEAFEJEJ_01056 | 4.4e-43 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
FEAFEJEJ_01057 | 1.9e-209 | ftsW | D | Belongs to the SEDS family | ||
FEAFEJEJ_01058 | 0.0 | typA | T | GTP-binding protein TypA | ||
FEAFEJEJ_01059 | 1.6e-143 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
FEAFEJEJ_01060 | 7.9e-45 | yktA | S | Belongs to the UPF0223 family | ||
FEAFEJEJ_01061 | 7.1e-164 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
FEAFEJEJ_01062 | 2e-269 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
FEAFEJEJ_01063 | 2.9e-206 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
FEAFEJEJ_01064 | 2.8e-182 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
FEAFEJEJ_01065 | 7e-214 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
FEAFEJEJ_01066 | 2.8e-102 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
FEAFEJEJ_01067 | 3.1e-68 | |||||
FEAFEJEJ_01068 | 1.2e-32 | ykzG | S | Belongs to the UPF0356 family | ||
FEAFEJEJ_01069 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
FEAFEJEJ_01070 | 5.7e-188 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic | |
FEAFEJEJ_01071 | 1.3e-28 | |||||
FEAFEJEJ_01072 | 1.6e-110 | mltD | CBM50 | M | NlpC P60 family protein | |
FEAFEJEJ_01073 | 3.7e-164 | ypuA | S | Protein of unknown function (DUF1002) | ||
FEAFEJEJ_01074 | 1.6e-168 | ykfC | 3.4.14.13 | M | NlpC/P60 family | |
FEAFEJEJ_01075 | 0.0 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
FEAFEJEJ_01076 | 2.8e-160 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
FEAFEJEJ_01077 | 3.6e-185 | rbsR | K | helix_turn _helix lactose operon repressor | ||
FEAFEJEJ_01078 | 1.1e-189 | yghZ | C | Aldo keto reductase family protein | ||
FEAFEJEJ_01079 | 9e-159 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
FEAFEJEJ_01080 | 1.6e-307 | E | ABC transporter, substratebinding protein | |||
FEAFEJEJ_01081 | 3.4e-280 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
FEAFEJEJ_01082 | 1.3e-159 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
FEAFEJEJ_01083 | 2.5e-121 | yecS | E | ABC transporter permease | ||
FEAFEJEJ_01084 | 4.5e-126 | yoaK | S | Protein of unknown function (DUF1275) | ||
FEAFEJEJ_01085 | 1.4e-176 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
FEAFEJEJ_01086 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
FEAFEJEJ_01087 | 1.5e-118 | S | Repeat protein | |||
FEAFEJEJ_01088 | 1e-119 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
FEAFEJEJ_01089 | 4.5e-224 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
FEAFEJEJ_01090 | 1.5e-58 | XK27_04120 | S | Putative amino acid metabolism | ||
FEAFEJEJ_01091 | 1.4e-223 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
FEAFEJEJ_01092 | 9.4e-124 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
FEAFEJEJ_01093 | 5.2e-31 | |||||
FEAFEJEJ_01094 | 2.5e-95 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
FEAFEJEJ_01095 | 2.2e-34 | cspA | K | Cold shock protein | ||
FEAFEJEJ_01096 | 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) | |
FEAFEJEJ_01097 | 3.3e-92 | divIVA | D | DivIVA domain protein | ||
FEAFEJEJ_01098 | 1.5e-146 | ylmH | S | S4 domain protein | ||
FEAFEJEJ_01099 | 4.1e-41 | yggT | S | YGGT family | ||
FEAFEJEJ_01100 | 1.7e-75 | 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 | ||
FEAFEJEJ_01101 | 1.1e-215 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
FEAFEJEJ_01102 | 2e-244 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
FEAFEJEJ_01103 | 1.8e-148 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
FEAFEJEJ_01104 | 1.1e-200 | 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) |
FEAFEJEJ_01105 | 4e-251 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
FEAFEJEJ_01106 | 1.9e-183 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
FEAFEJEJ_01107 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
FEAFEJEJ_01108 | 7.6e-62 | ftsL | D | Cell division protein FtsL | ||
FEAFEJEJ_01109 | 1.7e-176 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
FEAFEJEJ_01110 | 2e-79 | mraZ | K | Belongs to the MraZ family | ||
FEAFEJEJ_01111 | 7.5e-61 | S | Protein of unknown function (DUF3397) | |||
FEAFEJEJ_01112 | 2.2e-12 | S | Protein of unknown function (DUF4044) | |||
FEAFEJEJ_01113 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
FEAFEJEJ_01114 | 2.7e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
FEAFEJEJ_01115 | 4.8e-162 | rrmA | 2.1.1.187 | H | Methyltransferase | |
FEAFEJEJ_01116 | 1.6e-203 | XK27_05220 | S | AI-2E family transporter | ||
FEAFEJEJ_01117 | 1.9e-107 | cutC | P | Participates in the control of copper homeostasis | ||
FEAFEJEJ_01118 | 5.5e-16 | tagE1 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
FEAFEJEJ_01119 | 2.1e-269 | tagE3 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
FEAFEJEJ_01120 | 5.6e-270 | tagE2 | 2.4.1.52 | GT4 | M | Glycosyl transferases group 1 |
FEAFEJEJ_01121 | 1.9e-27 | |||||
FEAFEJEJ_01122 | 1.3e-63 | S | Pfam Methyltransferase | |||
FEAFEJEJ_01123 | 8.4e-60 | alr | 5.1.1.1, 6.3.2.10 | M | UDP-N-acetylmuramoyl-tripeptide-D-alanyl-D-alanine ligase activity | |
FEAFEJEJ_01124 | 3.1e-28 | 3.1.3.18 | S | Pfam Methyltransferase | ||
FEAFEJEJ_01125 | 3.7e-47 | 3.1.3.18 | S | Pfam Methyltransferase | ||
FEAFEJEJ_01126 | 2.6e-174 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
FEAFEJEJ_01127 | 6.8e-150 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
FEAFEJEJ_01128 | 3.3e-118 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
FEAFEJEJ_01129 | 1.4e-113 | yjbH | Q | Thioredoxin | ||
FEAFEJEJ_01130 | 2.5e-158 | degV | S | DegV family | ||
FEAFEJEJ_01131 | 0.0 | pepF | E | oligoendopeptidase F | ||
FEAFEJEJ_01132 | 1.4e-201 | coiA | 3.6.4.12 | S | Competence protein | |
FEAFEJEJ_01133 | 3.6e-125 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
FEAFEJEJ_01134 | 1.9e-149 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
FEAFEJEJ_01135 | 5.9e-222 | ecsB | U | ABC transporter | ||
FEAFEJEJ_01136 | 3e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_01137 | 3.1e-83 | hit | FG | histidine triad | ||
FEAFEJEJ_01138 | 1.9e-50 | |||||
FEAFEJEJ_01139 | 9.1e-151 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
FEAFEJEJ_01140 | 6e-185 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |||
FEAFEJEJ_01141 | 0.0 | L | AAA domain | |||
FEAFEJEJ_01142 | 6.9e-231 | yhaO | L | Ser Thr phosphatase family protein | ||
FEAFEJEJ_01143 | 6.9e-51 | yheA | S | Belongs to the UPF0342 family | ||
FEAFEJEJ_01144 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
FEAFEJEJ_01145 | 4.7e-79 | argR | K | Regulates arginine biosynthesis genes | ||
FEAFEJEJ_01146 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
FEAFEJEJ_01148 | 1.1e-17 | |||||
FEAFEJEJ_01149 | 1.1e-231 | 3.2.1.96, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
FEAFEJEJ_01150 | 4e-98 | 1.5.1.3 | H | RibD C-terminal domain | ||
FEAFEJEJ_01151 | 8.6e-54 | S | Protein of unknown function (DUF1516) | |||
FEAFEJEJ_01152 | 1.6e-131 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
FEAFEJEJ_01153 | 2.3e-253 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
FEAFEJEJ_01154 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
FEAFEJEJ_01155 | 4.9e-120 | ntcA2 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Transcriptional regulator, Crp Fnr family | |
FEAFEJEJ_01156 | 3.1e-275 | pipD | E | Peptidase family C69 | ||
FEAFEJEJ_01157 | 1.3e-37 | |||||
FEAFEJEJ_01158 | 0.0 | |||||
FEAFEJEJ_01161 | 0.0 | uvrA3 | L | ABC transporter | ||
FEAFEJEJ_01162 | 4.3e-113 | L | PFAM Integrase catalytic region | |||
FEAFEJEJ_01163 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_01165 | 5.1e-47 | |||||
FEAFEJEJ_01166 | 1.2e-83 | V | VanZ like family | |||
FEAFEJEJ_01167 | 4.7e-82 | ohrR | K | Transcriptional regulator | ||
FEAFEJEJ_01168 | 2.3e-122 | S | CAAX protease self-immunity | |||
FEAFEJEJ_01169 | 5.6e-35 | |||||
FEAFEJEJ_01170 | 4.6e-177 | 1.1.1.26 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | ||
FEAFEJEJ_01171 | 0.0 | trePP | 2.4.1.216, 2.4.1.8, 3.1.3.12, 3.2.1.28 | GH37,GH65 | G | Glycosyl hydrolase family 65 central catalytic domain |
FEAFEJEJ_01172 | 1e-119 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
FEAFEJEJ_01173 | 1.2e-143 | S | haloacid dehalogenase-like hydrolase | |||
FEAFEJEJ_01174 | 4.5e-120 | dck | 2.7.1.74 | F | Deoxynucleoside kinase | |
FEAFEJEJ_01175 | 2.8e-30 | XK27_08430 | S | Staphylococcal protein of unknown function (DUF960) | ||
FEAFEJEJ_01176 | 3.9e-260 | bmr3 | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01177 | 3.7e-213 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
FEAFEJEJ_01178 | 1.5e-121 | |||||
FEAFEJEJ_01179 | 5.3e-62 | |||||
FEAFEJEJ_01180 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01181 | 2.5e-104 | |||||
FEAFEJEJ_01182 | 2.6e-52 | ybjQ | S | Belongs to the UPF0145 family | ||
FEAFEJEJ_01183 | 3.6e-91 | zmp2 | O | Zinc-dependent metalloprotease | ||
FEAFEJEJ_01198 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
FEAFEJEJ_01199 | 4.3e-36 | ykuJ | S | Protein of unknown function (DUF1797) | ||
FEAFEJEJ_01200 | 1.9e-184 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
FEAFEJEJ_01201 | 3.6e-196 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
FEAFEJEJ_01202 | 2.7e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
FEAFEJEJ_01203 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
FEAFEJEJ_01204 | 7.2e-40 | ptsH | G | phosphocarrier protein HPR | ||
FEAFEJEJ_01205 | 3.9e-30 | |||||
FEAFEJEJ_01206 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
FEAFEJEJ_01207 | 4e-214 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
FEAFEJEJ_01208 | 0.0 | pacL3 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
FEAFEJEJ_01209 | 9.2e-283 | pipD | E | Dipeptidase | ||
FEAFEJEJ_01210 | 8.2e-257 | nox | 1.6.3.4 | C | NADH oxidase | |
FEAFEJEJ_01211 | 8.3e-280 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
FEAFEJEJ_01212 | 1.3e-306 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
FEAFEJEJ_01213 | 3.1e-90 | |||||
FEAFEJEJ_01214 | 0.0 | 2.7.8.12 | M | glycerophosphotransferase | ||
FEAFEJEJ_01215 | 3.7e-157 | |||||
FEAFEJEJ_01216 | 2.6e-76 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
FEAFEJEJ_01217 | 1.2e-179 | yueF | S | AI-2E family transporter | ||
FEAFEJEJ_01218 | 2.2e-107 | ygaC | J | Belongs to the UPF0374 family | ||
FEAFEJEJ_01219 | 5.6e-39 | S | Bacteriocin-protection, YdeI or OmpD-Associated | |||
FEAFEJEJ_01220 | 3.2e-217 | pbpX2 | V | Beta-lactamase | ||
FEAFEJEJ_01221 | 1.2e-143 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
FEAFEJEJ_01222 | 1e-78 | fld | C | Flavodoxin | ||
FEAFEJEJ_01223 | 7.6e-158 | yihY | S | Belongs to the UPF0761 family | ||
FEAFEJEJ_01224 | 2.1e-157 | S | Nuclease-related domain | |||
FEAFEJEJ_01225 | 1.8e-212 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
FEAFEJEJ_01226 | 2.5e-159 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
FEAFEJEJ_01227 | 1.4e-175 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01228 | 2.4e-232 | gntP | EG | Gluconate | ||
FEAFEJEJ_01229 | 5.6e-77 | T | Universal stress protein family | |||
FEAFEJEJ_01231 | 3.5e-212 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
FEAFEJEJ_01232 | 3.9e-187 | mocA | S | Oxidoreductase | ||
FEAFEJEJ_01233 | 5.7e-64 | S | Domain of unknown function (DUF4828) | |||
FEAFEJEJ_01234 | 8.7e-147 | lys | M | Glycosyl hydrolases family 25 | ||
FEAFEJEJ_01235 | 3.2e-150 | gntR | K | rpiR family | ||
FEAFEJEJ_01236 | 2.1e-304 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
FEAFEJEJ_01237 | 4.3e-213 | gntP | EG | Gluconate | ||
FEAFEJEJ_01238 | 6.1e-233 | potE | E | amino acid | ||
FEAFEJEJ_01239 | 4.3e-250 | fucP | G | Major Facilitator Superfamily | ||
FEAFEJEJ_01240 | 2.5e-65 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
FEAFEJEJ_01241 | 2.4e-297 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
FEAFEJEJ_01242 | 8.7e-240 | pdp | 2.4.2.2, 2.4.2.4 | F | pyrimidine-nucleoside phosphorylase | |
FEAFEJEJ_01243 | 5.2e-173 | deoR | K | sugar-binding domain protein | ||
FEAFEJEJ_01244 | 1.7e-128 | deoD | 2.4.2.1, 2.4.2.28 | F | Purine nucleoside phosphorylase | |
FEAFEJEJ_01245 | 3.8e-234 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
FEAFEJEJ_01246 | 1.3e-120 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
FEAFEJEJ_01247 | 5.1e-37 | cro | K | Helix-turn-helix XRE-family like proteins | ||
FEAFEJEJ_01248 | 2.3e-57 | K | Helix-turn-helix XRE-family like proteins | |||
FEAFEJEJ_01249 | 1.3e-145 | 3.1.3.48 | T | Pfam:Y_phosphatase3C | ||
FEAFEJEJ_01250 | 5.4e-195 | C | Oxidoreductase | |||
FEAFEJEJ_01251 | 7.8e-55 | pduU | E | BMC | ||
FEAFEJEJ_01252 | 5.4e-220 | ackA | 2.7.2.1, 2.7.2.15 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
FEAFEJEJ_01253 | 1.1e-209 | pduQ | C | Iron-containing alcohol dehydrogenase | ||
FEAFEJEJ_01254 | 2.7e-266 | pduP | 1.2.1.87 | C | Aldehyde dehydrogenase family | |
FEAFEJEJ_01255 | 1.4e-81 | pduO | S | Haem-degrading | ||
FEAFEJEJ_01256 | 5.8e-103 | pduO | 2.5.1.17 | S | Cobalamin adenosyltransferase | |
FEAFEJEJ_01257 | 6e-42 | ccmL | CQ | Ethanolamine utilisation protein EutN/carboxysome | ||
FEAFEJEJ_01258 | 6.7e-90 | S | Putative propanediol utilisation | |||
FEAFEJEJ_01259 | 6.1e-114 | pduL | 2.3.1.222, 2.3.1.8 | Q | Involved in 1,2-propanediol (1,2-PD) degradation by catalyzing the conversion of propanoyl-CoA to propanoyl-phosphate | |
FEAFEJEJ_01260 | 4.9e-42 | pduA_4 | CQ | BMC | ||
FEAFEJEJ_01261 | 4.9e-159 | L | DDE domain | |||
FEAFEJEJ_01262 | 9.7e-83 | pduK | CQ | BMC | ||
FEAFEJEJ_01263 | 1.1e-56 | pduH | S | Dehydratase medium subunit | ||
FEAFEJEJ_01264 | 0.0 | pduG | D | Diol dehydratase reactivase ATPase-like domain | ||
FEAFEJEJ_01265 | 3e-90 | pduE | 4.2.1.28 | Q | Dehydratase small subunit | |
FEAFEJEJ_01266 | 2e-129 | pduD | 4.2.1.28, 4.2.1.30 | Q | Dehydratase medium subunit | |
FEAFEJEJ_01267 | 0.0 | pduC | 4.2.1.28 | Q | Dehydratase large subunit | |
FEAFEJEJ_01268 | 4.1e-130 | pduB | E | BMC | ||
FEAFEJEJ_01269 | 5.2e-41 | pduA_4 | CQ | BMC | ||
FEAFEJEJ_01270 | 6.9e-206 | K | helix_turn_helix, arabinose operon control protein | |||
FEAFEJEJ_01271 | 3.2e-127 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
FEAFEJEJ_01272 | 2.5e-42 | eutP | E | Ethanolamine utilisation - propanediol utilisation | ||
FEAFEJEJ_01273 | 8.3e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
FEAFEJEJ_01274 | 9.4e-189 | yegS | 2.7.1.107 | G | Lipid kinase | |
FEAFEJEJ_01275 | 6.5e-273 | gatB | 6.1.1.12, 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
FEAFEJEJ_01276 | 3.8e-276 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
FEAFEJEJ_01277 | 1.5e-49 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
FEAFEJEJ_01278 | 1.1e-193 | camS | S | sex pheromone | ||
FEAFEJEJ_01279 | 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 | |
FEAFEJEJ_01280 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
FEAFEJEJ_01281 | 8.6e-215 | purK2 | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
FEAFEJEJ_01282 | 5.1e-99 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
FEAFEJEJ_01283 | 4.9e-157 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
FEAFEJEJ_01284 | 2.8e-182 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
FEAFEJEJ_01285 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
FEAFEJEJ_01286 | 1.8e-269 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
FEAFEJEJ_01287 | 4.2e-173 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
FEAFEJEJ_01288 | 9.3e-283 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
FEAFEJEJ_01289 | 3.7e-179 | pdxB | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
FEAFEJEJ_01290 | 1.1e-144 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
FEAFEJEJ_01291 | 2.2e-132 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
FEAFEJEJ_01292 | 1.3e-33 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
FEAFEJEJ_01293 | 4.1e-175 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01294 | 4e-158 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
FEAFEJEJ_01295 | 3.8e-190 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
FEAFEJEJ_01296 | 1.4e-254 | yfnA | E | Amino Acid | ||
FEAFEJEJ_01297 | 6e-196 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
FEAFEJEJ_01298 | 4.8e-79 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
FEAFEJEJ_01299 | 6.8e-223 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
FEAFEJEJ_01300 | 1.1e-104 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
FEAFEJEJ_01301 | 8e-199 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
FEAFEJEJ_01302 | 6.9e-116 | ktrA | P | domain protein | ||
FEAFEJEJ_01303 | 1.4e-240 | ktrB | P | Potassium uptake protein | ||
FEAFEJEJ_01304 | 1.9e-194 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
FEAFEJEJ_01305 | 4.7e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
FEAFEJEJ_01306 | 1.3e-78 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
FEAFEJEJ_01307 | 3.6e-151 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
FEAFEJEJ_01308 | 2.7e-143 | ecfT | U | Transmembrane (T) component of an energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
FEAFEJEJ_01309 | 2.4e-161 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
FEAFEJEJ_01310 | 3.7e-151 | cbiO | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
FEAFEJEJ_01311 | 7.4e-62 | rplQ | J | Ribosomal protein L17 | ||
FEAFEJEJ_01312 | 8.2e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
FEAFEJEJ_01313 | 7.5e-62 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
FEAFEJEJ_01314 | 1.3e-60 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
FEAFEJEJ_01315 | 1.4e-33 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
FEAFEJEJ_01316 | 3.4e-123 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
FEAFEJEJ_01317 | 1.2e-233 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
FEAFEJEJ_01318 | 1.9e-69 | rplO | J | Binds to the 23S rRNA | ||
FEAFEJEJ_01319 | 3.8e-24 | rpmD | J | Ribosomal protein L30 | ||
FEAFEJEJ_01320 | 2.4e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
FEAFEJEJ_01321 | 6.6e-57 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
FEAFEJEJ_01322 | 3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
FEAFEJEJ_01323 | 1e-66 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
FEAFEJEJ_01324 | 6.8e-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 | ||
FEAFEJEJ_01325 | 2.1e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
FEAFEJEJ_01326 | 1.8e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
FEAFEJEJ_01327 | 4.3e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
FEAFEJEJ_01328 | 1.9e-40 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
FEAFEJEJ_01329 | 4.8e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
FEAFEJEJ_01330 | 7.8e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
FEAFEJEJ_01331 | 5.1e-119 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
FEAFEJEJ_01332 | 2.4e-54 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
FEAFEJEJ_01333 | 1.8e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
FEAFEJEJ_01334 | 6e-149 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
FEAFEJEJ_01335 | 2e-43 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
FEAFEJEJ_01336 | 3.2e-107 | rplD | J | Forms part of the polypeptide exit tunnel | ||
FEAFEJEJ_01337 | 6.1e-117 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
FEAFEJEJ_01338 | 8.9e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
FEAFEJEJ_01339 | 7.8e-236 | mepA | V | MATE efflux family protein | ||
FEAFEJEJ_01340 | 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 | ||
FEAFEJEJ_01341 | 6.4e-84 | 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 | ||
FEAFEJEJ_01342 | 1.2e-70 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
FEAFEJEJ_01343 | 1.3e-114 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
FEAFEJEJ_01344 | 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 | |
FEAFEJEJ_01345 | 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 | |
FEAFEJEJ_01346 | 5e-105 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_01347 | 1.6e-230 | L | Transposase | |||
FEAFEJEJ_01348 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
FEAFEJEJ_01349 | 4.4e-77 | ctsR | K | Belongs to the CtsR family | ||
FEAFEJEJ_01358 | 5.2e-213 | 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) | |
FEAFEJEJ_01359 | 7.3e-115 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
FEAFEJEJ_01360 | 1.8e-276 | lysP | E | amino acid | ||
FEAFEJEJ_01361 | 1e-24 | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
FEAFEJEJ_01362 | 3.2e-152 | I | alpha/beta hydrolase fold | |||
FEAFEJEJ_01363 | 9.4e-121 | lssY | 3.6.1.27 | I | phosphatase | |
FEAFEJEJ_01364 | 2.2e-73 | S | Threonine/Serine exporter, ThrE | |||
FEAFEJEJ_01365 | 1.6e-121 | thrE | S | Putative threonine/serine exporter | ||
FEAFEJEJ_01366 | 1.5e-120 | sirR | K | iron dependent repressor | ||
FEAFEJEJ_01367 | 3.1e-159 | czcD | P | cation diffusion facilitator family transporter | ||
FEAFEJEJ_01368 | 4.3e-103 | K | Acetyltransferase (GNAT) domain | |||
FEAFEJEJ_01369 | 1.9e-77 | merR | K | MerR HTH family regulatory protein | ||
FEAFEJEJ_01370 | 5.1e-268 | lmrB | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01372 | 1.9e-161 | L | An automated process has identified a potential problem with this gene model | |||
FEAFEJEJ_01373 | 4.3e-100 | S | Domain of unknown function (DUF4811) | |||
FEAFEJEJ_01374 | 1e-37 | yyaN | K | MerR HTH family regulatory protein | ||
FEAFEJEJ_01375 | 1.5e-108 | azlC | E | branched-chain amino acid | ||
FEAFEJEJ_01376 | 7.3e-50 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
FEAFEJEJ_01377 | 7.3e-231 | pyrP | F | Permease | ||
FEAFEJEJ_01378 | 3.4e-214 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_01379 | 1e-69 | |||||
FEAFEJEJ_01380 | 2.5e-89 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
FEAFEJEJ_01381 | 1.8e-106 | L | PFAM Integrase catalytic region | |||
FEAFEJEJ_01382 | 2.4e-55 | L | Helix-turn-helix domain | |||
FEAFEJEJ_01383 | 3.8e-87 | nimA | S | resistance protein | ||
FEAFEJEJ_01384 | 6.3e-105 | 3.2.2.20 | K | acetyltransferase | ||
FEAFEJEJ_01385 | 1.6e-140 | yejC | S | Protein of unknown function (DUF1003) | ||
FEAFEJEJ_01386 | 1.8e-164 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
FEAFEJEJ_01387 | 1.5e-52 | S | Glycine cleavage H-protein | |||
FEAFEJEJ_01390 | 5.5e-90 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
FEAFEJEJ_01391 | 1e-281 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
FEAFEJEJ_01392 | 3.2e-138 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
FEAFEJEJ_01393 | 7.3e-305 | araB | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | carbohydrate kinase FGGY | |
FEAFEJEJ_01394 | 1e-249 | araP | U | Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family | ||
FEAFEJEJ_01395 | 3.8e-196 | araR | K | Transcriptional regulator | ||
FEAFEJEJ_01396 | 2.2e-86 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
FEAFEJEJ_01397 | 4.2e-169 | K | transcriptional regulator, ArsR family | |||
FEAFEJEJ_01398 | 6.9e-09 | abf | G | Belongs to the glycosyl hydrolase 43 family | ||
FEAFEJEJ_01399 | 1.4e-68 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
FEAFEJEJ_01400 | 6.1e-170 | abf | G | Belongs to the glycosyl hydrolase 43 family | ||
FEAFEJEJ_01401 | 1.5e-236 | lacY | G | Oligosaccharide H symporter | ||
FEAFEJEJ_01402 | 5.7e-225 | abfA | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
FEAFEJEJ_01403 | 1.1e-32 | abfA | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
FEAFEJEJ_01404 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
FEAFEJEJ_01405 | 2.1e-70 | K | Transcriptional regulator | |||
FEAFEJEJ_01406 | 9e-96 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
FEAFEJEJ_01407 | 1.8e-278 | pipD | E | Dipeptidase | ||
FEAFEJEJ_01408 | 1.8e-262 | arcD | E | Arginine ornithine antiporter | ||
FEAFEJEJ_01409 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
FEAFEJEJ_01410 | 1.4e-71 | S | Iron-sulphur cluster biosynthesis | |||
FEAFEJEJ_01411 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
FEAFEJEJ_01412 | 1.1e-305 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
FEAFEJEJ_01413 | 2.9e-102 | aacA4_1 | 4.1.1.17 | K | acetyltransferase | |
FEAFEJEJ_01414 | 2.4e-175 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
FEAFEJEJ_01415 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
FEAFEJEJ_01416 | 1.7e-289 | yjbQ | P | TrkA C-terminal domain protein | ||
FEAFEJEJ_01417 | 9.1e-121 | G | phosphoglycerate mutase | |||
FEAFEJEJ_01418 | 1.3e-179 | oppF | P | Belongs to the ABC transporter superfamily | ||
FEAFEJEJ_01419 | 3.5e-205 | oppD | P | Belongs to the ABC transporter superfamily | ||
FEAFEJEJ_01420 | 7.5e-186 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
FEAFEJEJ_01421 | 2.2e-152 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
FEAFEJEJ_01422 | 2.2e-304 | oppA | E | ABC transporter, substratebinding protein | ||
FEAFEJEJ_01423 | 1.9e-305 | oppA | E | ABC transporter, substratebinding protein | ||
FEAFEJEJ_01424 | 1.3e-224 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
FEAFEJEJ_01425 | 6.2e-109 | glnP | P | ABC transporter permease | ||
FEAFEJEJ_01426 | 1.1e-110 | gluC | P | ABC transporter permease | ||
FEAFEJEJ_01427 | 2.4e-150 | glnH | ET | ABC transporter substrate-binding protein | ||
FEAFEJEJ_01428 | 1.6e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
FEAFEJEJ_01429 | 1.2e-171 | |||||
FEAFEJEJ_01430 | 5.3e-13 | 3.2.1.14 | GH18 | |||
FEAFEJEJ_01431 | 3.9e-78 | zur | P | Belongs to the Fur family | ||
FEAFEJEJ_01432 | 2.3e-75 | gmk2 | 2.7.4.8 | F | Guanylate kinase | |
FEAFEJEJ_01433 | 2.4e-74 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
FEAFEJEJ_01434 | 2.5e-240 | yfnA | E | Amino Acid | ||
FEAFEJEJ_01435 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
FEAFEJEJ_01436 | 3.9e-178 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
FEAFEJEJ_01437 | 4.6e-87 | M | ErfK YbiS YcfS YnhG | |||
FEAFEJEJ_01438 | 2.3e-295 | S | ABC transporter, ATP-binding protein | |||
FEAFEJEJ_01439 | 4e-68 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
FEAFEJEJ_01440 | 6e-123 | XK27_07075 | S | CAAX protease self-immunity | ||
FEAFEJEJ_01441 | 7.5e-121 | cmpC | S | ATPases associated with a variety of cellular activities | ||
FEAFEJEJ_01442 | 2.3e-168 | WQ51_06230 | U | Belongs to the binding-protein-dependent transport system permease family | ||
FEAFEJEJ_01443 | 1.5e-167 | XK27_00670 | S | ABC transporter | ||
FEAFEJEJ_01444 | 1.6e-163 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
FEAFEJEJ_01445 | 8.6e-179 | XK27_08835 | S | ABC transporter | ||
FEAFEJEJ_01446 | 3e-154 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
FEAFEJEJ_01447 | 3.3e-138 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_01449 | 3.6e-157 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
FEAFEJEJ_01450 | 2e-127 | terC | P | integral membrane protein, YkoY family | ||
FEAFEJEJ_01451 | 9.1e-245 | pbpX1 | V | SH3-like domain | ||
FEAFEJEJ_01452 | 1.2e-109 | NU | mannosyl-glycoprotein | |||
FEAFEJEJ_01453 | 3.8e-162 | S | DUF218 domain | |||
FEAFEJEJ_01454 | 4.8e-190 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
FEAFEJEJ_01455 | 4.5e-135 | IQ | reductase | |||
FEAFEJEJ_01456 | 1.9e-15 | |||||
FEAFEJEJ_01457 | 0.0 | ydgH | S | MMPL family | ||
FEAFEJEJ_01458 | 1.3e-257 | ydiC1 | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01459 | 1.6e-91 | K | Transcriptional regulator PadR-like family | |||
FEAFEJEJ_01460 | 2.7e-82 | merR | K | MerR family regulatory protein | ||
FEAFEJEJ_01461 | 4.8e-63 | iap | CBM50 | M | NlpC P60 family | |
FEAFEJEJ_01462 | 8.3e-78 | yjcF | K | protein acetylation | ||
FEAFEJEJ_01463 | 9e-124 | pgm3 | G | phosphoglycerate mutase family | ||
FEAFEJEJ_01464 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
FEAFEJEJ_01465 | 2.9e-182 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
FEAFEJEJ_01466 | 4.7e-145 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
FEAFEJEJ_01467 | 8.7e-190 | S | Protease prsW family | |||
FEAFEJEJ_01468 | 3.5e-177 | iunH2 | 3.2.2.1, 3.2.2.8 | F | nucleoside hydrolase | |
FEAFEJEJ_01469 | 1e-173 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_01470 | 1.6e-07 | yvlA | ||||
FEAFEJEJ_01471 | 2.7e-88 | |||||
FEAFEJEJ_01472 | 2.4e-150 | XK27_02985 | S | Sucrose-6F-phosphate phosphohydrolase | ||
FEAFEJEJ_01473 | 1.6e-154 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
FEAFEJEJ_01474 | 6.8e-237 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
FEAFEJEJ_01475 | 1.4e-102 | S | Uncharacterized protein conserved in bacteria (DUF2087) | |||
FEAFEJEJ_01476 | 6.9e-68 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
FEAFEJEJ_01477 | 2.7e-60 | S | LuxR family transcriptional regulator | |||
FEAFEJEJ_01478 | 7.4e-134 | cat | 2.3.1.28 | V | Chloramphenicol acetyltransferase | |
FEAFEJEJ_01479 | 5.9e-219 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
FEAFEJEJ_01480 | 1.6e-168 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
FEAFEJEJ_01481 | 4.4e-95 | S | ABC transporter permease | |||
FEAFEJEJ_01482 | 7.7e-258 | P | ABC transporter | |||
FEAFEJEJ_01483 | 7.5e-115 | P | Cobalt transport protein | |||
FEAFEJEJ_01484 | 1.2e-120 | 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 | |
FEAFEJEJ_01485 | 6.6e-60 | |||||
FEAFEJEJ_01486 | 3.7e-176 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01487 | 1.1e-08 | |||||
FEAFEJEJ_01489 | 5.5e-32 | |||||
FEAFEJEJ_01490 | 2.1e-216 | |||||
FEAFEJEJ_01491 | 6.7e-187 | ansA | 3.5.1.1 | EJ | Asparaginase | |
FEAFEJEJ_01492 | 1.8e-24 | |||||
FEAFEJEJ_01493 | 8.5e-249 | pbuX | F | xanthine permease | ||
FEAFEJEJ_01494 | 7.2e-169 | natA | S | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_01495 | 4.7e-211 | natB | CP | ABC-2 family transporter protein | ||
FEAFEJEJ_01497 | 3.9e-251 | yjjP | S | Putative threonine/serine exporter | ||
FEAFEJEJ_01498 | 2e-160 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
FEAFEJEJ_01499 | 1.3e-153 | 1.1.1.2, 1.1.1.307 | C | Aldo keto reductase | ||
FEAFEJEJ_01500 | 2.1e-54 | S | Protein of unknown function (DUF1722) | |||
FEAFEJEJ_01501 | 2.6e-69 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
FEAFEJEJ_01502 | 3.1e-283 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
FEAFEJEJ_01503 | 5.8e-126 | K | Crp-like helix-turn-helix domain | |||
FEAFEJEJ_01504 | 4.3e-239 | larA | 5.1.2.1 | S | Domain of unknown function (DUF2088) | |
FEAFEJEJ_01505 | 1.2e-132 | cpmA | S | AIR carboxylase | ||
FEAFEJEJ_01506 | 1.6e-230 | larC | 4.99.1.12 | S | Involved in the biosynthesis of a nickel-pincer cofactor ((SCS)Ni(II) pincer complex). Binds Ni(2 ), and functions in nickel delivery to pyridinium-3,5-bisthiocarboxylic acid mononucleotide (P2TMN), to form the mature cofactor. Is thus probably required for the activation of nickel-pincer cofactor- dependent enzymes | |
FEAFEJEJ_01507 | 9.2e-150 | larE | S | NAD synthase | ||
FEAFEJEJ_01508 | 2.5e-121 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
FEAFEJEJ_01509 | 1.4e-178 | hoxN | U | High-affinity nickel-transport protein | ||
FEAFEJEJ_01510 | 2.3e-40 | GnaT | 2.5.1.16 | K | Acetyltransferase (GNAT) domain | |
FEAFEJEJ_01513 | 3.1e-209 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
FEAFEJEJ_01514 | 1.4e-147 | potB | P | ABC transporter permease | ||
FEAFEJEJ_01515 | 6.8e-134 | potC | P | ABC transporter permease | ||
FEAFEJEJ_01516 | 6.8e-206 | potD | P | ABC transporter | ||
FEAFEJEJ_01517 | 4.8e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
FEAFEJEJ_01518 | 5.2e-143 | pstA | P | Phosphate transport system permease protein PstA | ||
FEAFEJEJ_01519 | 1e-168 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
FEAFEJEJ_01520 | 1e-154 | pstS | P | Phosphate | ||
FEAFEJEJ_01521 | 1.1e-56 | |||||
FEAFEJEJ_01522 | 2.1e-31 | |||||
FEAFEJEJ_01523 | 5.3e-43 | |||||
FEAFEJEJ_01524 | 0.0 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
FEAFEJEJ_01525 | 1.7e-125 | |||||
FEAFEJEJ_01526 | 5.5e-180 | sepS16B | ||||
FEAFEJEJ_01527 | 9.8e-286 | V | ABC transporter transmembrane region | |||
FEAFEJEJ_01528 | 0.0 | KLT | Protein kinase domain | |||
FEAFEJEJ_01530 | 1e-198 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
FEAFEJEJ_01531 | 4.8e-81 | yoaA | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
FEAFEJEJ_01532 | 1e-298 | E | amino acid | |||
FEAFEJEJ_01533 | 5.4e-119 | S | membrane | |||
FEAFEJEJ_01534 | 4.6e-115 | S | VIT family | |||
FEAFEJEJ_01535 | 5.7e-91 | perR | P | Belongs to the Fur family | ||
FEAFEJEJ_01536 | 7.1e-179 | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase | |
FEAFEJEJ_01538 | 1e-126 | yibF | S | overlaps another CDS with the same product name | ||
FEAFEJEJ_01539 | 2.8e-202 | yibE | S | overlaps another CDS with the same product name | ||
FEAFEJEJ_01541 | 9.6e-83 | uspA | T | Belongs to the universal stress protein A family | ||
FEAFEJEJ_01542 | 7e-132 | |||||
FEAFEJEJ_01543 | 1.5e-86 | K | helix_turn_helix multiple antibiotic resistance protein | |||
FEAFEJEJ_01544 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
FEAFEJEJ_01546 | 6.3e-173 | |||||
FEAFEJEJ_01547 | 0.0 | M | domain protein | |||
FEAFEJEJ_01548 | 1.3e-44 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
FEAFEJEJ_01549 | 9.5e-92 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
FEAFEJEJ_01550 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
FEAFEJEJ_01552 | 3.3e-186 | galR | K | Transcriptional regulator | ||
FEAFEJEJ_01553 | 7.7e-285 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
FEAFEJEJ_01554 | 3.1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
FEAFEJEJ_01555 | 5.1e-223 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
FEAFEJEJ_01556 | 5.2e-254 | gph | G | Transporter | ||
FEAFEJEJ_01557 | 2.4e-37 | |||||
FEAFEJEJ_01558 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
FEAFEJEJ_01559 | 1.4e-197 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
FEAFEJEJ_01560 | 2.2e-207 | mmgC | 1.3.8.1 | I | Acyl-CoA dehydrogenase, C-terminal domain | |
FEAFEJEJ_01561 | 1.1e-144 | etfB | C | Electron transfer flavoprotein domain | ||
FEAFEJEJ_01562 | 1.3e-176 | etfA | C | Electron transfer flavoprotein FAD-binding domain | ||
FEAFEJEJ_01563 | 4.3e-186 | 1.1.1.1 | C | nadph quinone reductase | ||
FEAFEJEJ_01564 | 3.8e-54 | K | Transcriptional | |||
FEAFEJEJ_01565 | 3.4e-126 | hchA | 3.5.1.124 | S | DJ-1/PfpI family | |
FEAFEJEJ_01566 | 0.0 | oppD | EP | Psort location Cytoplasmic, score | ||
FEAFEJEJ_01567 | 6.3e-81 | 6.3.3.2 | S | ASCH | ||
FEAFEJEJ_01568 | 3e-246 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_01569 | 2.3e-23 | |||||
FEAFEJEJ_01570 | 1.9e-152 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
FEAFEJEJ_01571 | 7.4e-140 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
FEAFEJEJ_01572 | 1.4e-158 | hipB | K | Helix-turn-helix | ||
FEAFEJEJ_01573 | 1.3e-119 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
FEAFEJEJ_01574 | 7.5e-70 | yeaO | S | Protein of unknown function, DUF488 | ||
FEAFEJEJ_01575 | 1.2e-123 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | HAD-hyrolase-like |
FEAFEJEJ_01576 | 7.9e-79 | usp1 | T | Universal stress protein family | ||
FEAFEJEJ_01577 | 6.2e-264 | U | Belongs to the BCCT transporter (TC 2.A.15) family | |||
FEAFEJEJ_01578 | 9.1e-115 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
FEAFEJEJ_01579 | 2.5e-83 | S | 3-demethylubiquinone-9 3-methyltransferase | |||
FEAFEJEJ_01580 | 2.6e-146 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
FEAFEJEJ_01581 | 4.5e-85 | |||||
FEAFEJEJ_01582 | 6.4e-240 | codA | 3.5.4.1 | F | cytosine deaminase | |
FEAFEJEJ_01583 | 1.4e-47 | |||||
FEAFEJEJ_01584 | 1.1e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
FEAFEJEJ_01585 | 5.2e-18 | |||||
FEAFEJEJ_01586 | 1.1e-124 | yrkL | S | Flavodoxin-like fold | ||
FEAFEJEJ_01588 | 6.2e-30 | |||||
FEAFEJEJ_01590 | 1e-37 | S | Cytochrome B5 | |||
FEAFEJEJ_01591 | 2.1e-31 | cspC | K | Cold shock protein | ||
FEAFEJEJ_01592 | 1.6e-111 | XK27_00220 | S | Dienelactone hydrolase family | ||
FEAFEJEJ_01593 | 4.4e-52 | |||||
FEAFEJEJ_01594 | 7.9e-221 | mutY | L | A G-specific adenine glycosylase | ||
FEAFEJEJ_01595 | 4.7e-307 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
FEAFEJEJ_01596 | 0.0 | pelX | M | domain, Protein | ||
FEAFEJEJ_01597 | 1.1e-52 | |||||
FEAFEJEJ_01598 | 4.7e-196 | 6.3.1.20 | H | Lipoate-protein ligase | ||
FEAFEJEJ_01599 | 9.7e-67 | gcvH | E | glycine cleavage | ||
FEAFEJEJ_01600 | 1.5e-183 | tas | C | Aldo/keto reductase family | ||
FEAFEJEJ_01601 | 2.1e-32 | |||||
FEAFEJEJ_01602 | 1.6e-177 | EG | EamA-like transporter family | |||
FEAFEJEJ_01603 | 8.6e-114 | metI | P | ABC transporter permease | ||
FEAFEJEJ_01604 | 2e-194 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
FEAFEJEJ_01605 | 3.5e-146 | P | Belongs to the nlpA lipoprotein family | |||
FEAFEJEJ_01606 | 1.3e-99 | tag | 3.2.2.20 | L | glycosylase | |
FEAFEJEJ_01607 | 0.0 | E | ABC transporter, substratebinding protein | |||
FEAFEJEJ_01609 | 0.0 | 3.2.1.21 | GH3 | G | hydrolase, family 3 | |
FEAFEJEJ_01610 | 1.3e-192 | pva1 | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
FEAFEJEJ_01611 | 9.3e-288 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
FEAFEJEJ_01612 | 9.1e-209 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
FEAFEJEJ_01613 | 5.5e-106 | tag | 3.2.2.20 | L | glycosylase | |
FEAFEJEJ_01614 | 1.3e-144 | S | Zinc-dependent metalloprotease | |||
FEAFEJEJ_01615 | 2.5e-167 | XK27_00880 | 3.5.1.28 | M | hydrolase, family 25 | |
FEAFEJEJ_01616 | 6e-205 | G | Glycosyl hydrolases family 8 | |||
FEAFEJEJ_01617 | 8.6e-56 | yphJ | 4.1.1.44 | S | decarboxylase | |
FEAFEJEJ_01618 | 5.1e-80 | yphH | S | Cupin domain | ||
FEAFEJEJ_01619 | 2e-76 | K | helix_turn_helix, mercury resistance | |||
FEAFEJEJ_01620 | 2e-100 | yobS | K | Bacterial regulatory proteins, tetR family | ||
FEAFEJEJ_01621 | 1.2e-09 | K | MarR family | |||
FEAFEJEJ_01622 | 3.9e-229 | |||||
FEAFEJEJ_01623 | 1.1e-158 | dkgB | S | reductase | ||
FEAFEJEJ_01624 | 1.6e-203 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_01625 | 1.6e-195 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_01626 | 2.2e-134 | C | Oxidoreductase | |||
FEAFEJEJ_01627 | 1.9e-40 | ccmL | CQ | Ethanolamine utilisation protein EutN/carboxysome | ||
FEAFEJEJ_01628 | 5.9e-58 | K | helix_turn_helix, arabinose operon control protein | |||
FEAFEJEJ_01629 | 2.6e-228 | L | Transposase | |||
FEAFEJEJ_01630 | 1.4e-161 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_01631 | 4.3e-236 | L | Transposase | |||
FEAFEJEJ_01632 | 1.2e-52 | S | Domain of unknown function (DUF4430) | |||
FEAFEJEJ_01633 | 5.9e-178 | U | FFAT motif binding | |||
FEAFEJEJ_01634 | 3.6e-114 | S | ECF-type riboflavin transporter, S component | |||
FEAFEJEJ_01635 | 5.6e-308 | ykoD_2 | S | AAA domain, putative AbiEii toxin, Type IV TA system | ||
FEAFEJEJ_01636 | 1.1e-158 | P | ABC-type cobalt transport system permease component CbiQ and related transporters | |||
FEAFEJEJ_01637 | 2.1e-70 | |||||
FEAFEJEJ_01638 | 9.4e-98 | ubiX | 2.5.1.129 | H | Flavin prenyltransferase that catalyzes the synthesis of the prenylated FMN cofactor (prenyl-FMN) for 4-hydroxy-3- polyprenylbenzoic acid decarboxylase UbiD. The prenyltransferase is metal-independent and links a dimethylallyl moiety from dimethylallyl monophosphate (DMAP) to the flavin N5 and C6 atoms of FMN | |
FEAFEJEJ_01639 | 3.8e-284 | ubiD | 4.1.1.98 | H | 3-octaprenyl-4-hydroxybenzoate carboxy-lyase | |
FEAFEJEJ_01640 | 3.5e-160 | K | LysR substrate binding domain | |||
FEAFEJEJ_01641 | 4.6e-70 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
FEAFEJEJ_01642 | 0.0 | epsA | I | PAP2 superfamily | ||
FEAFEJEJ_01643 | 3e-54 | S | Domain of unknown function (DU1801) | |||
FEAFEJEJ_01644 | 3.2e-110 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
FEAFEJEJ_01645 | 6.8e-110 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
FEAFEJEJ_01646 | 0.0 | lmrA | 3.6.3.44 | V | ABC transporter | |
FEAFEJEJ_01647 | 2e-97 | rmaB | K | Transcriptional regulator, MarR family | ||
FEAFEJEJ_01648 | 4.8e-123 | S | membrane transporter protein | |||
FEAFEJEJ_01649 | 1.6e-112 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
FEAFEJEJ_01650 | 2.4e-120 | |||||
FEAFEJEJ_01651 | 3.9e-125 | skfE | V | ATPases associated with a variety of cellular activities | ||
FEAFEJEJ_01652 | 1.9e-62 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
FEAFEJEJ_01653 | 4.1e-178 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
FEAFEJEJ_01654 | 3.4e-85 | btuE | 1.11.1.9 | O | Belongs to the glutathione peroxidase family | |
FEAFEJEJ_01655 | 3.3e-130 | S | haloacid dehalogenase-like hydrolase | |||
FEAFEJEJ_01656 | 7.4e-206 | bcr1 | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01657 | 5.9e-146 | S | Sucrose-6F-phosphate phosphohydrolase | |||
FEAFEJEJ_01658 | 1.6e-156 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
FEAFEJEJ_01659 | 1e-101 | |||||
FEAFEJEJ_01661 | 7.5e-132 | ydfG | S | KR domain | ||
FEAFEJEJ_01662 | 8e-66 | hxlR | K | HxlR-like helix-turn-helix | ||
FEAFEJEJ_01663 | 7.4e-60 | asp2 | S | Asp23 family, cell envelope-related function | ||
FEAFEJEJ_01664 | 4.3e-71 | asp | S | Asp23 family, cell envelope-related function | ||
FEAFEJEJ_01665 | 3.4e-25 | |||||
FEAFEJEJ_01666 | 5.7e-92 | |||||
FEAFEJEJ_01667 | 8.8e-19 | S | Transglycosylase associated protein | |||
FEAFEJEJ_01668 | 4.5e-158 | |||||
FEAFEJEJ_01669 | 1.9e-270 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
FEAFEJEJ_01670 | 5.1e-138 | chaT1 | U | Major Facilitator Superfamily | ||
FEAFEJEJ_01671 | 2.8e-37 | chaT1 | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01672 | 2e-95 | laaE | K | Transcriptional regulator PadR-like family | ||
FEAFEJEJ_01673 | 2.1e-67 | lysM | M | LysM domain | ||
FEAFEJEJ_01674 | 1.2e-134 | XK27_07210 | 6.1.1.6 | S | B3 4 domain | |
FEAFEJEJ_01675 | 7.8e-123 | iprA | K | Cyclic nucleotide-monophosphate binding domain | ||
FEAFEJEJ_01676 | 1.8e-170 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
FEAFEJEJ_01677 | 2e-213 | arcT | 2.6.1.1 | E | Aminotransferase | |
FEAFEJEJ_01678 | 5.2e-201 | arcD | E | Arginine ornithine antiporter | ||
FEAFEJEJ_01679 | 1.3e-34 | arcD | E | Arginine ornithine antiporter | ||
FEAFEJEJ_01680 | 3.3e-197 | argF | 2.1.3.3, 2.1.3.6, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
FEAFEJEJ_01681 | 7.7e-238 | arcA | 3.5.3.6 | E | Arginine | |
FEAFEJEJ_01682 | 1.1e-281 | S | C4-dicarboxylate anaerobic carrier | |||
FEAFEJEJ_01683 | 4.2e-226 | 2.1.1.80, 2.7.13.3, 3.1.1.61 | T | histidine kinase DNA gyrase B | ||
FEAFEJEJ_01684 | 2.7e-149 | KT | YcbB domain | |||
FEAFEJEJ_01685 | 1.2e-280 | arcD | S | C4-dicarboxylate anaerobic carrier | ||
FEAFEJEJ_01686 | 1.3e-259 | ytjP | 3.5.1.18 | E | Dipeptidase | |
FEAFEJEJ_01688 | 1.2e-208 | ykiI | ||||
FEAFEJEJ_01689 | 4.5e-106 | thiJ-2 | 3.5.1.124 | S | DJ-1/PfpI family | |
FEAFEJEJ_01690 | 3.5e-161 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
FEAFEJEJ_01691 | 3.5e-76 | L | Transposase DDE domain | |||
FEAFEJEJ_01692 | 5.1e-68 | L | Putative transposase of IS4/5 family (DUF4096) | |||
FEAFEJEJ_01693 | 3.6e-220 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_01694 | 1.2e-36 | S | Protein of unknown function (DUF3781) | |||
FEAFEJEJ_01695 | 7.5e-39 | |||||
FEAFEJEJ_01696 | 1.2e-84 | yafP | 3.6.4.13 | K | Acetyltransferase (GNAT) domain | |
FEAFEJEJ_01697 | 1.2e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
FEAFEJEJ_01698 | 1.4e-268 | M | domain protein | |||
FEAFEJEJ_01699 | 1.8e-169 | K | AI-2E family transporter | |||
FEAFEJEJ_01700 | 4.3e-214 | xylR | GK | ROK family | ||
FEAFEJEJ_01701 | 2.7e-118 | |||||
FEAFEJEJ_01702 | 5.7e-238 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
FEAFEJEJ_01703 | 7.7e-188 | L | Helix-turn-helix domain | |||
FEAFEJEJ_01704 | 4.3e-53 | azlD | S | branched-chain amino acid | ||
FEAFEJEJ_01705 | 8.5e-137 | azlC | E | AzlC protein | ||
FEAFEJEJ_01706 | 1.3e-87 | ywnH | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
FEAFEJEJ_01707 | 2.9e-254 | gor | 1.8.1.7 | C | Glutathione reductase | |
FEAFEJEJ_01709 | 8.5e-38 | S | Domain of unknown function (DUF4430) | |||
FEAFEJEJ_01710 | 7.9e-230 | L | Transposase | |||
FEAFEJEJ_01711 | 2.3e-161 | V | domain protein | |||
FEAFEJEJ_01712 | 4.4e-239 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
FEAFEJEJ_01713 | 8.7e-215 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
FEAFEJEJ_01714 | 3.5e-123 | K | response regulator | |||
FEAFEJEJ_01715 | 2.8e-210 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
FEAFEJEJ_01716 | 3e-107 | |||||
FEAFEJEJ_01717 | 3.1e-133 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
FEAFEJEJ_01718 | 4.4e-200 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
FEAFEJEJ_01719 | 7.2e-32 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
FEAFEJEJ_01720 | 3.4e-155 | spo0J | K | Belongs to the ParB family | ||
FEAFEJEJ_01721 | 4.1e-136 | soj | D | Sporulation initiation inhibitor | ||
FEAFEJEJ_01722 | 5e-148 | noc | K | Belongs to the ParB family | ||
FEAFEJEJ_01723 | 1.7e-131 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
FEAFEJEJ_01724 | 1.3e-162 | cpdA | 2.1.2.2, 3.1.4.17, 3.1.4.53 | S | Calcineurin-like phosphoesterase | |
FEAFEJEJ_01725 | 2.3e-170 | rihC | 3.2.2.1, 3.2.2.8 | F | Nucleoside | |
FEAFEJEJ_01726 | 3.7e-214 | pbuO_1 | S | Permease family | ||
FEAFEJEJ_01727 | 1.4e-226 | nupG | F | Nucleoside | ||
FEAFEJEJ_01728 | 2.1e-154 | 5.4.2.7 | G | Metalloenzyme superfamily | ||
FEAFEJEJ_01729 | 3.7e-114 | GM | NmrA-like family | |||
FEAFEJEJ_01730 | 8.2e-44 | |||||
FEAFEJEJ_01731 | 5.6e-10 | |||||
FEAFEJEJ_01732 | 2.9e-62 | |||||
FEAFEJEJ_01733 | 4.1e-40 | |||||
FEAFEJEJ_01734 | 1.1e-62 | K | HxlR-like helix-turn-helix | |||
FEAFEJEJ_01735 | 1.2e-34 | |||||
FEAFEJEJ_01736 | 6.4e-119 | |||||
FEAFEJEJ_01737 | 0.0 | |||||
FEAFEJEJ_01738 | 2.4e-219 | |||||
FEAFEJEJ_01739 | 3.4e-123 | |||||
FEAFEJEJ_01740 | 3.5e-214 | EK | Aminotransferase, class I | |||
FEAFEJEJ_01741 | 1.7e-165 | K | LysR substrate binding domain | |||
FEAFEJEJ_01742 | 4.8e-11 | S | Protein of unknown function (DUF2922) | |||
FEAFEJEJ_01743 | 5.1e-27 | |||||
FEAFEJEJ_01744 | 6.4e-99 | K | DNA-templated transcription, initiation | |||
FEAFEJEJ_01745 | 1.7e-204 | |||||
FEAFEJEJ_01746 | 5.5e-65 | |||||
FEAFEJEJ_01747 | 1.2e-54 | |||||
FEAFEJEJ_01748 | 1.5e-194 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
FEAFEJEJ_01749 | 1.7e-229 | macB3 | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_01750 | 1.6e-37 | macB3 | V | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_01751 | 2e-112 | thiE | 2.5.1.3 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
FEAFEJEJ_01752 | 4.9e-148 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
FEAFEJEJ_01753 | 3.4e-138 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
FEAFEJEJ_01754 | 8.2e-73 | vdlC | S | Enoyl-(Acyl carrier protein) reductase | ||
FEAFEJEJ_01755 | 4.9e-159 | L | DDE domain | |||
FEAFEJEJ_01756 | 2e-69 | vdlC | S | Enoyl-(Acyl carrier protein) reductase | ||
FEAFEJEJ_01757 | 2.8e-129 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
FEAFEJEJ_01758 | 4.2e-118 | ybbL | S | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_01759 | 6.1e-274 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
FEAFEJEJ_01760 | 3.7e-74 | |||||
FEAFEJEJ_01761 | 3.5e-88 | rmeB | K | transcriptional regulator, MerR family | ||
FEAFEJEJ_01762 | 4.6e-96 | J | glyoxalase III activity | |||
FEAFEJEJ_01763 | 1.2e-133 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
FEAFEJEJ_01764 | 3.6e-134 | K | helix_turn_helix, mercury resistance | |||
FEAFEJEJ_01765 | 1.8e-223 | xylR | GK | ROK family | ||
FEAFEJEJ_01766 | 2.9e-159 | akr5f | 1.1.1.346 | C | Aldo keto reductase | |
FEAFEJEJ_01767 | 5.2e-248 | rarA | L | recombination factor protein RarA | ||
FEAFEJEJ_01768 | 2.8e-280 | rny | S | Endoribonuclease that initiates mRNA decay | ||
FEAFEJEJ_01769 | 5.4e-127 | yoaK | S | Protein of unknown function (DUF1275) | ||
FEAFEJEJ_01770 | 1.6e-174 | D | Alpha beta | |||
FEAFEJEJ_01771 | 0.0 | pepF2 | E | Oligopeptidase F | ||
FEAFEJEJ_01772 | 5.4e-74 | K | Transcriptional regulator | |||
FEAFEJEJ_01773 | 3e-164 | |||||
FEAFEJEJ_01774 | 3.3e-192 | S | DUF218 domain | |||
FEAFEJEJ_01775 | 1.5e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
FEAFEJEJ_01776 | 3.7e-157 | nanK | 2.7.1.2 | GK | ROK family | |
FEAFEJEJ_01777 | 6.1e-252 | frlA | E | Amino acid permease | ||
FEAFEJEJ_01778 | 1.5e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
FEAFEJEJ_01779 | 1.2e-34 | S | SEC-C Motif Domain Protein | |||
FEAFEJEJ_01780 | 1.4e-194 | S | DNA/RNA non-specific endonuclease | |||
FEAFEJEJ_01782 | 2e-52 | |||||
FEAFEJEJ_01783 | 3e-78 | K | Winged helix DNA-binding domain | |||
FEAFEJEJ_01784 | 1.3e-111 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the epimerization of the S- and R-forms of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration. This is a prerequisite for the S- specific NAD(P)H-hydrate dehydratase to allow the repair of both epimers of NAD(P)HX | |
FEAFEJEJ_01785 | 2.3e-104 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
FEAFEJEJ_01786 | 7.9e-114 | |||||
FEAFEJEJ_01787 | 1.5e-183 | pva3 | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
FEAFEJEJ_01788 | 3.8e-84 | iap | CBM50 | M | NlpC P60 family | |
FEAFEJEJ_01789 | 1.1e-118 | L | Transposase | |||
FEAFEJEJ_01790 | 2.3e-60 | L | Transposase | |||
FEAFEJEJ_01791 | 1.4e-161 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_01792 | 1.4e-292 | ytgP | S | Polysaccharide biosynthesis protein | ||
FEAFEJEJ_01793 | 3.8e-60 | K | Helix-turn-helix domain | |||
FEAFEJEJ_01794 | 0.0 | yuxL | 3.4.19.1 | E | Prolyl oligopeptidase family | |
FEAFEJEJ_01795 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_01796 | 3.1e-170 | panE2 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
FEAFEJEJ_01797 | 8.8e-44 | |||||
FEAFEJEJ_01798 | 1.9e-65 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
FEAFEJEJ_01799 | 0.0 | yjcE | P | Sodium proton antiporter | ||
FEAFEJEJ_01800 | 4.4e-311 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
FEAFEJEJ_01801 | 2.4e-306 | astA | 2.8.2.22 | M | Arylsulfotransferase Ig-like domain | |
FEAFEJEJ_01802 | 4.9e-117 | yoaK | S | Protein of unknown function (DUF1275) | ||
FEAFEJEJ_01803 | 8.1e-155 | rihA | F | Inosine-uridine preferring nucleoside hydrolase | ||
FEAFEJEJ_01805 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_01806 | 1.9e-178 | K | helix_turn _helix lactose operon repressor | |||
FEAFEJEJ_01807 | 6.1e-29 | mcbG | S | Pentapeptide repeats (8 copies) | ||
FEAFEJEJ_01808 | 1e-99 | ywlG | S | Belongs to the UPF0340 family | ||
FEAFEJEJ_01809 | 4e-84 | hmpT | S | ECF-type riboflavin transporter, S component | ||
FEAFEJEJ_01810 | 2.2e-140 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | Phosphomethylpyrimidine kinase | |
FEAFEJEJ_01811 | 1.6e-260 | norG_2 | K | Aminotransferase class I and II | ||
FEAFEJEJ_01812 | 4.5e-202 | lytR5 | K | Cell envelope-related transcriptional attenuator domain | ||
FEAFEJEJ_01813 | 7e-12 | lytR5 | K | Cell envelope-related transcriptional attenuator domain | ||
FEAFEJEJ_01814 | 1e-139 | P | ATPases associated with a variety of cellular activities | |||
FEAFEJEJ_01815 | 1.9e-144 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
FEAFEJEJ_01816 | 8.6e-102 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
FEAFEJEJ_01817 | 3.5e-76 | L | Transposase DDE domain | |||
FEAFEJEJ_01818 | 5.1e-68 | L | Putative transposase of IS4/5 family (DUF4096) | |||
FEAFEJEJ_01819 | 6e-216 | rodA | D | Cell cycle protein | ||
FEAFEJEJ_01820 | 4.3e-95 | |||||
FEAFEJEJ_01822 | 3.1e-71 | 4.4.1.5 | E | Glyoxalase | ||
FEAFEJEJ_01823 | 7.3e-141 | S | Membrane | |||
FEAFEJEJ_01824 | 2.8e-185 | tdh | 1.1.1.14 | C | Zinc-binding dehydrogenase | |
FEAFEJEJ_01825 | 6.8e-172 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
FEAFEJEJ_01826 | 4.4e-76 | |||||
FEAFEJEJ_01827 | 1.9e-203 | gldA | 1.1.1.6 | C | dehydrogenase | |
FEAFEJEJ_01828 | 5.7e-55 | ykkC | P | Small Multidrug Resistance protein | ||
FEAFEJEJ_01829 | 9.7e-52 | sugE | P | Multidrug resistance protein | ||
FEAFEJEJ_01830 | 1.8e-106 | speG | J | Acetyltransferase (GNAT) domain | ||
FEAFEJEJ_01831 | 3.6e-146 | G | Belongs to the phosphoglycerate mutase family | |||
FEAFEJEJ_01833 | 0.0 | treP | 2.4.1.64 | GH65 | G | hydrolase, family 65, central catalytic |
FEAFEJEJ_01834 | 2e-194 | nlhH_1 | I | alpha/beta hydrolase fold | ||
FEAFEJEJ_01835 | 4.9e-249 | xylP2 | G | symporter | ||
FEAFEJEJ_01836 | 1e-08 | yoeB | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | ||
FEAFEJEJ_01837 | 3.9e-17 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
FEAFEJEJ_01838 | 1.7e-304 | E | ABC transporter, substratebinding protein | |||
FEAFEJEJ_01839 | 4.9e-82 | |||||
FEAFEJEJ_01840 | 2.1e-08 | |||||
FEAFEJEJ_01841 | 2.5e-178 | K | Transcriptional regulator, LacI family | |||
FEAFEJEJ_01842 | 3e-262 | G | Major Facilitator | |||
FEAFEJEJ_01843 | 0.0 | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain protein | |
FEAFEJEJ_01844 | 3.6e-117 | |||||
FEAFEJEJ_01845 | 1.4e-74 | K | helix_turn_helix, mercury resistance | |||
FEAFEJEJ_01846 | 1.9e-53 | napB | K | Transcriptional regulator | ||
FEAFEJEJ_01847 | 3.1e-111 | 1.6.5.5 | C | alcohol dehydrogenase | ||
FEAFEJEJ_01848 | 3.7e-72 | 2.3.1.209, 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | ||
FEAFEJEJ_01849 | 1.9e-43 | C | Oxidoreductase | |||
FEAFEJEJ_01851 | 1.3e-09 | M | COG3209 Rhs family protein | |||
FEAFEJEJ_01852 | 3.3e-183 | mdt(A) | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01853 | 1.5e-222 | C | Oxidoreductase | |||
FEAFEJEJ_01854 | 3.1e-12 | |||||
FEAFEJEJ_01855 | 1.2e-67 | K | Transcriptional regulator, HxlR family | |||
FEAFEJEJ_01856 | 6.8e-214 | mccF | V | LD-carboxypeptidase | ||
FEAFEJEJ_01857 | 2.8e-179 | rihB | 3.2.2.1, 3.2.2.8 | F | Nucleoside | |
FEAFEJEJ_01858 | 8.9e-119 | yeiL | K | Cyclic nucleotide-monophosphate binding domain | ||
FEAFEJEJ_01859 | 3.1e-173 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
FEAFEJEJ_01860 | 6.3e-221 | dhaT | 1.1.1.1, 1.1.1.202 | C | Dehydrogenase | |
FEAFEJEJ_01861 | 1.8e-135 | hadL | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
FEAFEJEJ_01862 | 2.8e-122 | S | GyrI-like small molecule binding domain | |||
FEAFEJEJ_01863 | 3.7e-69 | ycgX | S | Protein of unknown function (DUF1398) | ||
FEAFEJEJ_01864 | 2.1e-99 | S | Phosphatidylethanolamine-binding protein | |||
FEAFEJEJ_01865 | 9.2e-224 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_01866 | 7.8e-123 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
FEAFEJEJ_01867 | 2.6e-181 | hrtB | V | ABC transporter permease | ||
FEAFEJEJ_01868 | 2.4e-87 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
FEAFEJEJ_01869 | 6.8e-207 | ynfM | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01870 | 1.4e-84 | thiW | S | Thiamine-precursor transporter protein (ThiW) | ||
FEAFEJEJ_01871 | 1.5e-167 | mleP | S | Sodium Bile acid symporter family | ||
FEAFEJEJ_01872 | 1e-309 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
FEAFEJEJ_01873 | 1.1e-161 | mleR | K | LysR family | ||
FEAFEJEJ_01874 | 5.8e-149 | K | Helix-turn-helix domain, rpiR family | |||
FEAFEJEJ_01875 | 6.1e-218 | aguA | 3.5.3.12 | E | agmatine deiminase | |
FEAFEJEJ_01876 | 3.8e-154 | arcC | 2.7.2.2 | E | Belongs to the carbamate kinase family | |
FEAFEJEJ_01877 | 1e-217 | aguA | 3.5.3.12 | E | agmatine deiminase | |
FEAFEJEJ_01878 | 9.9e-234 | aguD | E | Amino Acid | ||
FEAFEJEJ_01879 | 2.5e-197 | ptcA | 2.1.3.3, 2.1.3.6 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
FEAFEJEJ_01880 | 3.1e-238 | nhaC | C | Na H antiporter NhaC | ||
FEAFEJEJ_01881 | 6.8e-262 | E | Amino acid permease | |||
FEAFEJEJ_01882 | 0.0 | tdc | 4.1.1.25 | E | Pyridoxal-dependent decarboxylase conserved domain | |
FEAFEJEJ_01883 | 2.2e-240 | 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) | |
FEAFEJEJ_01884 | 1.3e-38 | |||||
FEAFEJEJ_01887 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01888 | 2.7e-208 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
FEAFEJEJ_01889 | 1.9e-26 | |||||
FEAFEJEJ_01890 | 6.3e-157 | EG | EamA-like transporter family | |||
FEAFEJEJ_01891 | 2.6e-304 | abfA | 3.2.1.55 | GH51 | G | Alpha-L-arabinofuranosidase C-terminus |
FEAFEJEJ_01892 | 2.3e-38 | |||||
FEAFEJEJ_01893 | 6.4e-14 | S | Transglycosylase associated protein | |||
FEAFEJEJ_01894 | 7.8e-14 | yjdF | S | Protein of unknown function (DUF2992) | ||
FEAFEJEJ_01895 | 1.2e-157 | K | Transcriptional regulator | |||
FEAFEJEJ_01896 | 3.7e-306 | 3.2.1.45 | GH30 | G | Glycosyl hydrolase family 30 TIM-barrel domain | |
FEAFEJEJ_01898 | 2.9e-29 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
FEAFEJEJ_01899 | 2.9e-09 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
FEAFEJEJ_01901 | 3.9e-10 | |||||
FEAFEJEJ_01902 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01903 | 3.2e-138 | S | Belongs to the UPF0246 family | |||
FEAFEJEJ_01904 | 7.6e-112 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
FEAFEJEJ_01905 | 5.3e-122 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
FEAFEJEJ_01906 | 7.5e-217 | naiP | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01907 | 1.7e-131 | S | Protein of unknown function | |||
FEAFEJEJ_01908 | 3e-175 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
FEAFEJEJ_01909 | 2.1e-165 | G | Belongs to the carbohydrate kinase PfkB family | |||
FEAFEJEJ_01910 | 1.3e-257 | F | Belongs to the purine-cytosine permease (2.A.39) family | |||
FEAFEJEJ_01911 | 2.6e-191 | yegU | O | ADP-ribosylglycohydrolase | ||
FEAFEJEJ_01912 | 2.3e-122 | yihL | K | UTRA | ||
FEAFEJEJ_01913 | 4.5e-157 | yhaZ | L | DNA alkylation repair enzyme | ||
FEAFEJEJ_01914 | 4e-127 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
FEAFEJEJ_01915 | 0.0 | tetP | J | elongation factor G | ||
FEAFEJEJ_01916 | 3.9e-234 | EK | Aminotransferase, class I | |||
FEAFEJEJ_01917 | 3.6e-17 | |||||
FEAFEJEJ_01918 | 2.1e-70 | S | COG NOG18757 non supervised orthologous group | |||
FEAFEJEJ_01919 | 2e-174 | pmrB | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01920 | 1.2e-109 | lacA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
FEAFEJEJ_01921 | 7.2e-81 | |||||
FEAFEJEJ_01922 | 1.5e-25 | |||||
FEAFEJEJ_01923 | 4.9e-119 | cah | 4.2.1.1 | P | Eukaryotic-type carbonic anhydrase | |
FEAFEJEJ_01924 | 1.3e-223 | LO | Uncharacterized conserved protein (DUF2075) | |||
FEAFEJEJ_01925 | 2e-26 | K | Transcriptional | |||
FEAFEJEJ_01926 | 3.4e-71 | |||||
FEAFEJEJ_01927 | 0.0 | M | Mycoplasma protein of unknown function, DUF285 | |||
FEAFEJEJ_01928 | 4.2e-112 | S | NADPH-dependent FMN reductase | |||
FEAFEJEJ_01929 | 1.4e-175 | L | Integrase core domain | |||
FEAFEJEJ_01930 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_01931 | 1.5e-141 | U | Binding-protein-dependent transport system inner membrane component | |||
FEAFEJEJ_01932 | 2.6e-152 | U | Binding-protein-dependent transport system inner membrane component | |||
FEAFEJEJ_01933 | 1.6e-249 | G | Bacterial extracellular solute-binding protein | |||
FEAFEJEJ_01934 | 1.9e-214 | P | Belongs to the ABC transporter superfamily | |||
FEAFEJEJ_01935 | 3.4e-172 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
FEAFEJEJ_01936 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
FEAFEJEJ_01937 | 9.8e-71 | K | Transcriptional regulator | |||
FEAFEJEJ_01938 | 1.9e-94 | qorB | 1.6.5.2 | GM | NmrA-like family | |
FEAFEJEJ_01939 | 1.7e-211 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
FEAFEJEJ_01940 | 5.8e-76 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
FEAFEJEJ_01942 | 1.1e-141 | K | Helix-turn-helix domain | |||
FEAFEJEJ_01943 | 1.7e-176 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01944 | 4.7e-168 | |||||
FEAFEJEJ_01945 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
FEAFEJEJ_01946 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
FEAFEJEJ_01947 | 9.1e-217 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
FEAFEJEJ_01948 | 6.2e-185 | xynD | 3.5.1.104 | G | polysaccharide deacetylase | |
FEAFEJEJ_01949 | 1.3e-58 | |||||
FEAFEJEJ_01950 | 4.6e-103 | GM | NAD(P)H-binding | |||
FEAFEJEJ_01951 | 5.7e-183 | iolS | C | Aldo keto reductase | ||
FEAFEJEJ_01952 | 5.9e-228 | pbuG | S | permease | ||
FEAFEJEJ_01953 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_01954 | 1.7e-93 | K | helix_turn_helix multiple antibiotic resistance protein | |||
FEAFEJEJ_01955 | 1.7e-165 | drrA | V | ABC transporter | ||
FEAFEJEJ_01956 | 7e-120 | drrB | U | ABC-2 type transporter | ||
FEAFEJEJ_01957 | 1.5e-169 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
FEAFEJEJ_01958 | 0.0 | S | Bacterial membrane protein YfhO | |||
FEAFEJEJ_01959 | 1.2e-86 | ccl | S | QueT transporter | ||
FEAFEJEJ_01960 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_01961 | 2.2e-32 | |||||
FEAFEJEJ_01962 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
FEAFEJEJ_01963 | 0.0 | xynB | 3.2.1.37 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
FEAFEJEJ_01964 | 2.7e-282 | xynT | G | MFS/sugar transport protein | ||
FEAFEJEJ_01965 | 5.3e-151 | rhaS2 | K | Transcriptional regulator, AraC family | ||
FEAFEJEJ_01966 | 9.7e-280 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
FEAFEJEJ_01967 | 5.2e-22 | |||||
FEAFEJEJ_01968 | 9.1e-150 | F | DNA/RNA non-specific endonuclease | |||
FEAFEJEJ_01969 | 4.5e-89 | |||||
FEAFEJEJ_01972 | 1.2e-51 | |||||
FEAFEJEJ_01973 | 9e-113 | L | haloacid dehalogenase-like hydrolase | |||
FEAFEJEJ_01974 | 3.5e-252 | pepC | 3.4.22.40 | E | aminopeptidase | |
FEAFEJEJ_01975 | 1.6e-79 | K | helix_turn_helix multiple antibiotic resistance protein | |||
FEAFEJEJ_01976 | 4.2e-109 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
FEAFEJEJ_01977 | 5.3e-218 | tcaB | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_01978 | 1.6e-227 | S | module of peptide synthetase | |||
FEAFEJEJ_01979 | 1.2e-91 | ykhA | 3.1.2.20 | I | Thioesterase superfamily | |
FEAFEJEJ_01980 | 1.4e-98 | J | Acetyltransferase (GNAT) domain | |||
FEAFEJEJ_01981 | 5.1e-116 | ywnB | S | NAD(P)H-binding | ||
FEAFEJEJ_01982 | 5.5e-245 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
FEAFEJEJ_01983 | 4.3e-37 | |||||
FEAFEJEJ_01984 | 2.6e-126 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
FEAFEJEJ_01985 | 5.1e-37 | |||||
FEAFEJEJ_01986 | 5.5e-48 | |||||
FEAFEJEJ_01987 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
FEAFEJEJ_01988 | 3.2e-256 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
FEAFEJEJ_01989 | 5.9e-111 | jag | S | R3H domain protein | ||
FEAFEJEJ_01990 | 1e-145 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
FEAFEJEJ_01991 | 3.2e-59 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
FEAFEJEJ_01992 | 2.6e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
FEAFEJEJ_01993 | 1.7e-257 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
FEAFEJEJ_01994 | 6.5e-207 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
FEAFEJEJ_01995 | 6e-35 | yaaA | S | S4 domain protein YaaA | ||
FEAFEJEJ_01996 | 1.7e-210 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
FEAFEJEJ_01997 | 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 | |
FEAFEJEJ_01998 | 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 | |
FEAFEJEJ_01999 | 1.9e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
FEAFEJEJ_02000 | 3e-59 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
FEAFEJEJ_02001 | 1.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
FEAFEJEJ_02002 | 4.7e-232 | Q | Imidazolonepropionase and related amidohydrolases | |||
FEAFEJEJ_02003 | 4e-303 | E | ABC transporter, substratebinding protein | |||
FEAFEJEJ_02004 | 2.4e-144 | |||||
FEAFEJEJ_02005 | 9.7e-230 | Q | Imidazolonepropionase and related amidohydrolases | |||
FEAFEJEJ_02006 | 1.8e-303 | E | ABC transporter, substratebinding protein | |||
FEAFEJEJ_02007 | 2.9e-99 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_02008 | 1e-38 | S | response to heat | |||
FEAFEJEJ_02009 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
FEAFEJEJ_02010 | 7.2e-64 | rplI | J | Binds to the 23S rRNA | ||
FEAFEJEJ_02012 | 6e-255 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
FEAFEJEJ_02013 | 3.8e-101 | S | NADPH-dependent FMN reductase | |||
FEAFEJEJ_02014 | 1.1e-212 | yttB | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02015 | 1.1e-22 | |||||
FEAFEJEJ_02016 | 2.8e-304 | E | ABC transporter, substratebinding protein | |||
FEAFEJEJ_02017 | 1.3e-38 | |||||
FEAFEJEJ_02018 | 5.7e-130 | E | Matrixin | |||
FEAFEJEJ_02020 | 5.7e-132 | K | response regulator | |||
FEAFEJEJ_02021 | 0.0 | vicK | 2.7.13.3 | T | Histidine kinase | |
FEAFEJEJ_02022 | 7.4e-239 | yycH | S | YycH protein | ||
FEAFEJEJ_02023 | 4.7e-149 | yycI | S | YycH protein | ||
FEAFEJEJ_02024 | 3.4e-157 | vicX | 3.1.26.11 | S | domain protein | |
FEAFEJEJ_02025 | 3.4e-194 | htrA | 3.4.21.107 | O | serine protease | |
FEAFEJEJ_02026 | 3.6e-82 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
FEAFEJEJ_02027 | 1.7e-06 | S | Protein of unknown function (DUF2971) | |||
FEAFEJEJ_02028 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02029 | 2.2e-193 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02031 | 1.2e-82 | |||||
FEAFEJEJ_02032 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
FEAFEJEJ_02033 | 6.5e-79 | K | Acetyltransferase (GNAT) domain | |||
FEAFEJEJ_02034 | 7.2e-166 | |||||
FEAFEJEJ_02035 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02036 | 4.3e-108 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
FEAFEJEJ_02037 | 3.4e-09 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | M | Bacterial surface protein 26-residue PARCEL repeat (3 repeats) | |
FEAFEJEJ_02038 | 2.1e-14 | S | Mor transcription activator family | |||
FEAFEJEJ_02039 | 2.9e-25 | ydhO | 3.4.14.13 | M | NlpC/P60 family | |
FEAFEJEJ_02040 | 3.1e-105 | ydhO | 3.4.14.13 | M | NlpC/P60 family | |
FEAFEJEJ_02041 | 4.3e-236 | L | Transposase | |||
FEAFEJEJ_02042 | 5.1e-119 | lsa | S | ABC transporter | ||
FEAFEJEJ_02043 | 1.8e-81 | argO | S | LysE type translocator | ||
FEAFEJEJ_02044 | 1.3e-35 | mgrA | K | helix_turn_helix multiple antibiotic resistance protein | ||
FEAFEJEJ_02045 | 4.3e-143 | nlhH | I | Esterase | ||
FEAFEJEJ_02046 | 1.6e-174 | draG | 3.2.2.24 | O | ADP-ribosylglycohydrolase | |
FEAFEJEJ_02047 | 8.4e-60 | yncA | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
FEAFEJEJ_02048 | 1.4e-68 | L | the current gene model (or a revised gene model) may contain a frame shift | |||
FEAFEJEJ_02049 | 2.1e-70 | L | Helix-turn-helix domain | |||
FEAFEJEJ_02050 | 4.3e-113 | L | PFAM Integrase catalytic region | |||
FEAFEJEJ_02052 | 4.7e-89 | cadD | P | Cadmium resistance transporter | ||
FEAFEJEJ_02053 | 8.3e-78 | lipB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
FEAFEJEJ_02054 | 1.7e-77 | gtrA | S | GtrA-like protein | ||
FEAFEJEJ_02055 | 1.5e-305 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
FEAFEJEJ_02056 | 2.8e-114 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_02057 | 3.6e-230 | XK27_06930 | S | ABC-2 family transporter protein | ||
FEAFEJEJ_02058 | 2e-131 | qmcA | O | prohibitin homologues | ||
FEAFEJEJ_02059 | 5.7e-55 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
FEAFEJEJ_02060 | 4.3e-135 | |||||
FEAFEJEJ_02061 | 5e-99 | GBS0088 | S | Nucleotidyltransferase | ||
FEAFEJEJ_02062 | 3.7e-85 | yybC | S | Protein of unknown function (DUF2798) | ||
FEAFEJEJ_02063 | 8.9e-57 | ydiI | Q | Thioesterase superfamily | ||
FEAFEJEJ_02064 | 1.1e-155 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
FEAFEJEJ_02065 | 7.8e-274 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
FEAFEJEJ_02066 | 6.1e-94 | S | Protein of unknown function (DUF1097) | |||
FEAFEJEJ_02067 | 1.1e-164 | |||||
FEAFEJEJ_02068 | 1e-287 | 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 | |
FEAFEJEJ_02069 | 2.2e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
FEAFEJEJ_02070 | 1.7e-213 | lmrP | E | Major Facilitator Superfamily | ||
FEAFEJEJ_02073 | 2.6e-100 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_02074 | 5.4e-181 | 1.1.1.1 | C | nadph quinone reductase | ||
FEAFEJEJ_02075 | 8.9e-107 | dhaS | K | Bacterial regulatory proteins, tetR family | ||
FEAFEJEJ_02076 | 9e-204 | E | amino acid | |||
FEAFEJEJ_02077 | 1e-60 | E | amino acid | |||
FEAFEJEJ_02078 | 6.5e-281 | gadB | 4.1.1.15 | E | Belongs to the group II decarboxylase family | |
FEAFEJEJ_02079 | 1.2e-293 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
FEAFEJEJ_02081 | 1.6e-171 | |||||
FEAFEJEJ_02082 | 1.8e-08 | asnB | 6.3.5.4 | E | Protein of unknown function (DUF3923) | |
FEAFEJEJ_02083 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02084 | 3.4e-228 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
FEAFEJEJ_02085 | 1e-107 | ahpC | 1.11.1.15 | O | Peroxiredoxin | |
FEAFEJEJ_02086 | 4.8e-60 | |||||
FEAFEJEJ_02087 | 3.8e-35 | ylbE | GM | NAD(P)H-binding | ||
FEAFEJEJ_02088 | 1.4e-175 | L | Integrase core domain | |||
FEAFEJEJ_02089 | 5.1e-66 | ylbE | GM | NAD(P)H-binding | ||
FEAFEJEJ_02090 | 1.1e-45 | |||||
FEAFEJEJ_02091 | 6.6e-17 | K | Helix-turn-helix XRE-family like proteins | |||
FEAFEJEJ_02092 | 3.2e-47 | K | Helix-turn-helix XRE-family like proteins | |||
FEAFEJEJ_02095 | 1.2e-274 | 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 | |
FEAFEJEJ_02096 | 1e-72 | K | Transcriptional regulator | |||
FEAFEJEJ_02097 | 4.2e-77 | elaA | S | Gnat family | ||
FEAFEJEJ_02098 | 6.2e-290 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
FEAFEJEJ_02099 | 2.5e-160 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
FEAFEJEJ_02100 | 4e-147 | 1.1.1.65 | C | Aldo keto reductase | ||
FEAFEJEJ_02101 | 3e-89 | |||||
FEAFEJEJ_02102 | 3.9e-215 | yttB | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02103 | 4.9e-246 | glpT | G | Major Facilitator Superfamily | ||
FEAFEJEJ_02104 | 5.2e-136 | nfrA | 1.5.1.39 | C | nitroreductase | |
FEAFEJEJ_02105 | 5.3e-86 | nrdI | F | Belongs to the NrdI family | ||
FEAFEJEJ_02106 | 1.8e-268 | S | ATPases associated with a variety of cellular activities | |||
FEAFEJEJ_02107 | 1.2e-250 | lmrB | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02109 | 2e-143 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
FEAFEJEJ_02110 | 1.9e-175 | K | Transcriptional regulator, LacI family | |||
FEAFEJEJ_02111 | 9.7e-242 | yhdP | S | Transporter associated domain | ||
FEAFEJEJ_02112 | 7.6e-61 | |||||
FEAFEJEJ_02113 | 1.4e-74 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
FEAFEJEJ_02114 | 7.1e-262 | yjeM | E | Amino Acid | ||
FEAFEJEJ_02115 | 3.6e-162 | ytbE | 1.1.1.346 | S | Aldo keto reductase | |
FEAFEJEJ_02116 | 1.9e-161 | L | An automated process has identified a potential problem with this gene model | |||
FEAFEJEJ_02117 | 0.0 | yfgQ | P | E1-E2 ATPase | ||
FEAFEJEJ_02118 | 5e-93 | M1-874 | K | Domain of unknown function (DUF1836) | ||
FEAFEJEJ_02119 | 0.0 | glpQ | 3.1.4.46 | C | phosphodiesterase | |
FEAFEJEJ_02120 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
FEAFEJEJ_02121 | 6.1e-52 | M | LysM domain protein | |||
FEAFEJEJ_02122 | 0.0 | 3.2.1.4, 3.2.1.78, 3.2.1.8 | GH26,GH5,GH9 | M | Leucine-rich repeat (LRR) protein | |
FEAFEJEJ_02123 | 2.1e-56 | M | LysM domain protein | |||
FEAFEJEJ_02125 | 6.5e-57 | M | LysM domain | |||
FEAFEJEJ_02127 | 2.7e-97 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_02128 | 1.9e-166 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
FEAFEJEJ_02129 | 5.1e-176 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
FEAFEJEJ_02130 | 1.6e-219 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
FEAFEJEJ_02131 | 1.1e-57 | DR0488 | S | 3D domain | ||
FEAFEJEJ_02132 | 6.3e-288 | M | Exporter of polyketide antibiotics | |||
FEAFEJEJ_02133 | 4.2e-169 | yjjC | V | ABC transporter | ||
FEAFEJEJ_02134 | 5.6e-118 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
FEAFEJEJ_02135 | 1.4e-234 | V | Polysaccharide biosynthesis C-terminal domain | |||
FEAFEJEJ_02136 | 2.9e-289 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
FEAFEJEJ_02137 | 1.4e-259 | gph | G | MFS/sugar transport protein | ||
FEAFEJEJ_02138 | 0.0 | yicI | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
FEAFEJEJ_02139 | 0.0 | uidA | 3.2.1.31 | G | Belongs to the glycosyl hydrolase 2 family | |
FEAFEJEJ_02140 | 0.0 | mtlD | 1.1.1.17, 1.1.1.57 | G | Mannitol dehydrogenase C-terminal domain | |
FEAFEJEJ_02141 | 1e-167 | yqhA | G | Aldose 1-epimerase | ||
FEAFEJEJ_02142 | 3.2e-121 | pgm3 | G | Belongs to the phosphoglycerate mutase family | ||
FEAFEJEJ_02143 | 1.4e-189 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |||
FEAFEJEJ_02144 | 2.7e-304 | gntK | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
FEAFEJEJ_02145 | 2.3e-170 | gnd | 1.1.1.343, 1.1.1.44 | G | Dehydrogenase | |
FEAFEJEJ_02146 | 2.6e-129 | kdgR | K | FCD domain | ||
FEAFEJEJ_02147 | 2e-213 | uxuA | 4.2.1.8 | G | Catalyzes the dehydration of D-mannonate | |
FEAFEJEJ_02148 | 2e-183 | exuR | K | Periplasmic binding protein domain | ||
FEAFEJEJ_02149 | 1.6e-277 | yjmB | G | MFS/sugar transport protein | ||
FEAFEJEJ_02150 | 4.8e-309 | 5.1.2.7 | S | tagaturonate epimerase | ||
FEAFEJEJ_02151 | 4e-294 | uxaC | 5.3.1.12 | G | glucuronate isomerase | |
FEAFEJEJ_02152 | 2.4e-226 | S | module of peptide synthetase | |||
FEAFEJEJ_02154 | 3.7e-252 | EGP | Major facilitator Superfamily | |||
FEAFEJEJ_02155 | 1e-16 | S | Protein of unknown function (DUF3278) | |||
FEAFEJEJ_02156 | 3.3e-15 | U | Bacterial surface protein 26-residue | |||
FEAFEJEJ_02157 | 1.2e-130 | |||||
FEAFEJEJ_02158 | 9.9e-91 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
FEAFEJEJ_02159 | 2e-132 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
FEAFEJEJ_02160 | 8.2e-125 | O | Zinc-dependent metalloprotease | |||
FEAFEJEJ_02161 | 3.9e-84 | 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 | ||
FEAFEJEJ_02162 | 1.8e-77 | |||||
FEAFEJEJ_02163 | 9.2e-141 | plnC | K | LytTr DNA-binding domain | ||
FEAFEJEJ_02164 | 6.2e-241 | 2.7.13.3 | T | GHKL domain | ||
FEAFEJEJ_02165 | 3.1e-240 | 2.1.1.80, 2.7.13.3, 3.1.1.61 | T | protein histidine kinase activity | ||
FEAFEJEJ_02166 | 4.1e-133 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
FEAFEJEJ_02168 | 2e-166 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
FEAFEJEJ_02169 | 2.8e-76 | uspA | T | universal stress protein | ||
FEAFEJEJ_02170 | 2.8e-105 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
FEAFEJEJ_02171 | 4.8e-92 | norB | EGP | Major Facilitator | ||
FEAFEJEJ_02172 | 6.1e-72 | norB | EGP | Major Facilitator | ||
FEAFEJEJ_02173 | 1.7e-11 | K | transcriptional regulator | |||
FEAFEJEJ_02174 | 5e-51 | K | transcriptional regulator | |||
FEAFEJEJ_02175 | 0.0 | oppA1 | E | ABC transporter substrate-binding protein | ||
FEAFEJEJ_02176 | 1e-173 | oppC | EP | Binding-protein-dependent transport system inner membrane component | ||
FEAFEJEJ_02177 | 9.8e-180 | oppB | P | ABC transporter permease | ||
FEAFEJEJ_02178 | 2.2e-179 | oppF | P | Belongs to the ABC transporter superfamily | ||
FEAFEJEJ_02179 | 2.4e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
FEAFEJEJ_02180 | 1.5e-80 | ywnA | K | Winged helix-turn-helix transcription repressor, HrcA DNA-binding | ||
FEAFEJEJ_02181 | 1.6e-196 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
FEAFEJEJ_02182 | 2.3e-69 | |||||
FEAFEJEJ_02183 | 2e-48 | |||||
FEAFEJEJ_02184 | 2.3e-267 | xylA | 5.3.1.5 | G | Belongs to the xylose isomerase family | |
FEAFEJEJ_02185 | 5.5e-294 | xylB | 2.7.1.12, 2.7.1.16, 2.7.1.17 | G | Xylulose kinase | |
FEAFEJEJ_02186 | 5.8e-226 | xylT | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02187 | 3.3e-141 | IQ | reductase | |||
FEAFEJEJ_02188 | 1.6e-69 | frataxin | S | Domain of unknown function (DU1801) | ||
FEAFEJEJ_02189 | 0.0 | S | membrane | |||
FEAFEJEJ_02190 | 3e-90 | uspA | T | universal stress protein | ||
FEAFEJEJ_02191 | 4.7e-96 | yxkA | S | Phosphatidylethanolamine-binding protein | ||
FEAFEJEJ_02192 | 1.4e-217 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
FEAFEJEJ_02193 | 3.9e-123 | kcsA | P | Ion channel | ||
FEAFEJEJ_02194 | 2.3e-49 | |||||
FEAFEJEJ_02195 | 5.3e-169 | C | Aldo keto reductase | |||
FEAFEJEJ_02196 | 7.5e-70 | |||||
FEAFEJEJ_02197 | 1.7e-93 | Z012_06855 | S | Acetyltransferase (GNAT) family | ||
FEAFEJEJ_02198 | 2.2e-252 | nhaC | C | Na H antiporter NhaC | ||
FEAFEJEJ_02199 | 2.3e-190 | S | Membrane transport protein | |||
FEAFEJEJ_02200 | 7e-189 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
FEAFEJEJ_02201 | 1.3e-277 | yufL | 2.7.13.3 | T | Single cache domain 3 | |
FEAFEJEJ_02202 | 3e-125 | malR3 | K | cheY-homologous receiver domain | ||
FEAFEJEJ_02203 | 1.6e-94 | S | ABC-2 family transporter protein | |||
FEAFEJEJ_02204 | 2.7e-61 | S | ABC-2 family transporter protein | |||
FEAFEJEJ_02205 | 1.4e-101 | XK27_06935 | K | Bacterial regulatory proteins, tetR family | ||
FEAFEJEJ_02206 | 1.5e-123 | yliE | T | Putative diguanylate phosphodiesterase | ||
FEAFEJEJ_02207 | 6.9e-95 | wecD | K | Acetyltransferase (GNAT) family | ||
FEAFEJEJ_02208 | 4.7e-141 | S | zinc-ribbon domain | |||
FEAFEJEJ_02209 | 1.6e-234 | S | response to antibiotic | |||
FEAFEJEJ_02211 | 1.2e-85 | F | NUDIX domain | |||
FEAFEJEJ_02213 | 3.2e-103 | padC | Q | Phenolic acid decarboxylase | ||
FEAFEJEJ_02214 | 1.8e-83 | padR | K | Virulence activator alpha C-term | ||
FEAFEJEJ_02215 | 5.3e-101 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_02216 | 4.7e-188 | 1.1.1.219 | GM | Male sterility protein | ||
FEAFEJEJ_02217 | 1.2e-76 | elaA | S | Gnat family | ||
FEAFEJEJ_02218 | 2.1e-79 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
FEAFEJEJ_02219 | 1.2e-73 | |||||
FEAFEJEJ_02220 | 3.4e-92 | |||||
FEAFEJEJ_02221 | 5e-91 | P | Cadmium resistance transporter | |||
FEAFEJEJ_02222 | 3.1e-121 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
FEAFEJEJ_02223 | 1.5e-71 | T | Universal stress protein family | |||
FEAFEJEJ_02224 | 2.4e-284 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
FEAFEJEJ_02225 | 7.7e-188 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
FEAFEJEJ_02226 | 3.7e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
FEAFEJEJ_02227 | 2.2e-243 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
FEAFEJEJ_02228 | 6.1e-97 | fadR | K | Bacterial regulatory proteins, tetR family | ||
FEAFEJEJ_02229 | 3.9e-181 | D | Alpha beta | |||
FEAFEJEJ_02230 | 1.1e-147 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
FEAFEJEJ_02231 | 5.7e-166 | I | Alpha beta | |||
FEAFEJEJ_02232 | 0.0 | O | Pro-kumamolisin, activation domain | |||
FEAFEJEJ_02233 | 8e-117 | S | Membrane | |||
FEAFEJEJ_02234 | 1.8e-133 | puuD | S | peptidase C26 | ||
FEAFEJEJ_02235 | 5.4e-37 | |||||
FEAFEJEJ_02236 | 2.4e-113 | magIII | L | Base excision DNA repair protein, HhH-GPD family | ||
FEAFEJEJ_02237 | 7.2e-294 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
FEAFEJEJ_02238 | 3.2e-200 | M | NlpC/P60 family | |||
FEAFEJEJ_02239 | 1.5e-163 | G | Peptidase_C39 like family | |||
FEAFEJEJ_02240 | 4.9e-243 | 3.2.1.21 | GH3 | G | Fibronectin type III-like domain | |
FEAFEJEJ_02241 | 6.8e-79 | K | AraC-like ligand binding domain | |||
FEAFEJEJ_02242 | 1.7e-247 | lacZ3 | 3.2.1.23 | G | Beta-galactosidase trimerisation domain | |
FEAFEJEJ_02243 | 1e-147 | blt | G | MFS/sugar transport protein | ||
FEAFEJEJ_02244 | 9e-216 | srfJ1 | 3.2.1.45 | GH30 | M | Belongs to the glycosyl hydrolase 30 family |
FEAFEJEJ_02245 | 4.5e-105 | pncA | Q | Isochorismatase family | ||
FEAFEJEJ_02246 | 1.5e-55 | K | Transcriptional regulator PadR-like family | |||
FEAFEJEJ_02247 | 6.3e-74 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
FEAFEJEJ_02248 | 1.3e-118 | S | Putative adhesin | |||
FEAFEJEJ_02249 | 1.2e-185 | 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 | ||
FEAFEJEJ_02250 | 6.6e-226 | fabV | 1.3.1.44, 1.3.1.9 | I | NAD(P)H binding domain of trans-2-enoyl-CoA reductase | |
FEAFEJEJ_02251 | 7.4e-74 | fld | C | Flavodoxin | ||
FEAFEJEJ_02252 | 3.9e-98 | K | Acetyltransferase (GNAT) domain | |||
FEAFEJEJ_02253 | 6.8e-243 | yifK | E | Amino acid permease | ||
FEAFEJEJ_02254 | 5.6e-118 | |||||
FEAFEJEJ_02255 | 5.5e-104 | S | WxL domain surface cell wall-binding | |||
FEAFEJEJ_02256 | 0.0 | XK27_00720 | S | Leucine-rich repeat (LRR) protein | ||
FEAFEJEJ_02257 | 5.8e-225 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
FEAFEJEJ_02258 | 7.9e-188 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
FEAFEJEJ_02259 | 8.8e-69 | lrpA | K | AsnC family | ||
FEAFEJEJ_02260 | 2.8e-163 | opuBA | E | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_02261 | 1.7e-274 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
FEAFEJEJ_02262 | 1.6e-202 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
FEAFEJEJ_02263 | 5.8e-100 | S | NADPH-dependent FMN reductase | |||
FEAFEJEJ_02264 | 9.2e-73 | K | MarR family | |||
FEAFEJEJ_02265 | 0.0 | pacL1 | P | P-type ATPase | ||
FEAFEJEJ_02267 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02268 | 1.9e-11 | pipD | E | Dipeptidase | ||
FEAFEJEJ_02269 | 2.6e-228 | L | Transposase | |||
FEAFEJEJ_02270 | 1.4e-161 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02271 | 7.6e-252 | pipD | E | Dipeptidase | ||
FEAFEJEJ_02272 | 1.6e-153 | |||||
FEAFEJEJ_02273 | 6.6e-99 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose O-acetyltransferase | |
FEAFEJEJ_02274 | 1.3e-119 | S | Elongation factor G-binding protein, N-terminal | |||
FEAFEJEJ_02275 | 4e-170 | EG | EamA-like transporter family | |||
FEAFEJEJ_02276 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
FEAFEJEJ_02277 | 1.7e-78 | copR | K | Copper transport repressor CopY TcrY | ||
FEAFEJEJ_02278 | 6.3e-227 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
FEAFEJEJ_02279 | 1.7e-159 | S | reductase | |||
FEAFEJEJ_02280 | 0.0 | ctpA | 3.6.3.54 | P | P-type ATPase | |
FEAFEJEJ_02281 | 2.5e-67 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
FEAFEJEJ_02283 | 5.6e-155 | yxkH | G | Polysaccharide deacetylase | ||
FEAFEJEJ_02284 | 1.1e-158 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
FEAFEJEJ_02285 | 1.3e-190 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
FEAFEJEJ_02286 | 0.0 | oatA | I | Acyltransferase | ||
FEAFEJEJ_02287 | 1.4e-120 | |||||
FEAFEJEJ_02288 | 0.0 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
FEAFEJEJ_02289 | 2.6e-106 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
FEAFEJEJ_02290 | 3.5e-67 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
FEAFEJEJ_02291 | 1.4e-37 | |||||
FEAFEJEJ_02292 | 2.4e-94 | K | helix_turn_helix multiple antibiotic resistance protein | |||
FEAFEJEJ_02293 | 1.2e-247 | xylP1 | G | MFS/sugar transport protein | ||
FEAFEJEJ_02294 | 4.6e-99 | S | Protein of unknown function (DUF1440) | |||
FEAFEJEJ_02295 | 0.0 | uvrA2 | L | ABC transporter | ||
FEAFEJEJ_02296 | 5e-66 | S | Tautomerase enzyme | |||
FEAFEJEJ_02297 | 1e-263 | |||||
FEAFEJEJ_02298 | 7.1e-221 | |||||
FEAFEJEJ_02299 | 2.1e-109 | opuCD | P | Binding-protein-dependent transport system inner membrane component | ||
FEAFEJEJ_02300 | 3.4e-177 | opuCC | M | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
FEAFEJEJ_02301 | 8e-106 | opuCB | E | ABC transporter permease | ||
FEAFEJEJ_02302 | 1.3e-154 | opuCA | E | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_02303 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02304 | 8.3e-61 | opuCA | E | ABC transporter, ATP-binding protein | ||
FEAFEJEJ_02305 | 2.1e-45 | |||||
FEAFEJEJ_02306 | 5.9e-222 | mdtG | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02307 | 5.5e-183 | yfeX | P | Peroxidase | ||
FEAFEJEJ_02308 | 1.4e-228 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
FEAFEJEJ_02309 | 6.2e-109 | M | Protein of unknown function (DUF3737) | |||
FEAFEJEJ_02310 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
FEAFEJEJ_02311 | 7.4e-194 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
FEAFEJEJ_02312 | 1.4e-161 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02313 | 2.6e-228 | L | Transposase | |||
FEAFEJEJ_02314 | 1.4e-248 | M | hydrolase, family 25 | |||
FEAFEJEJ_02315 | 3.3e-107 | |||||
FEAFEJEJ_02316 | 2e-195 | yubA | S | AI-2E family transporter | ||
FEAFEJEJ_02317 | 1.5e-166 | yclI | V | FtsX-like permease family | ||
FEAFEJEJ_02318 | 2.9e-122 | yclH | V | ABC transporter | ||
FEAFEJEJ_02319 | 0.0 | malL | 3.2.1.10, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31 | G | Alpha amylase, catalytic domain protein |
FEAFEJEJ_02320 | 8.6e-57 | K | Winged helix DNA-binding domain | |||
FEAFEJEJ_02321 | 1.1e-138 | pnuC | H | nicotinamide mononucleotide transporter | ||
FEAFEJEJ_02322 | 8.2e-152 | corA | P | CorA-like Mg2+ transporter protein | ||
FEAFEJEJ_02323 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
FEAFEJEJ_02324 | 4.1e-66 | |||||
FEAFEJEJ_02325 | 6.5e-43 | |||||
FEAFEJEJ_02326 | 7e-248 | T | PhoQ Sensor | |||
FEAFEJEJ_02327 | 8e-131 | K | Transcriptional regulatory protein, C terminal | |||
FEAFEJEJ_02328 | 1.2e-30 | |||||
FEAFEJEJ_02329 | 1.9e-115 | ylbE | GM | NAD(P)H-binding | ||
FEAFEJEJ_02330 | 6.5e-229 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
FEAFEJEJ_02331 | 8.1e-96 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
FEAFEJEJ_02332 | 1.7e-102 | K | Bacterial regulatory proteins, tetR family | |||
FEAFEJEJ_02333 | 2e-266 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
FEAFEJEJ_02334 | 1.2e-100 | K | Bacterial transcriptional regulator | |||
FEAFEJEJ_02335 | 1.4e-53 | kguE | 2.7.1.45 | G | Xylose isomerase-like TIM barrel | |
FEAFEJEJ_02336 | 6.2e-10 | |||||
FEAFEJEJ_02338 | 2.1e-146 | kduI | 5.3.1.17 | G | Catalyzes the isomerization of 5-dehydro-4-deoxy-D- glucuronate to 3-deoxy-D-glycero-2,5-hexodiulosonate | |
FEAFEJEJ_02339 | 1e-137 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
FEAFEJEJ_02340 | 7e-128 | kdgT | P | 2-keto-3-deoxygluconate permease | ||
FEAFEJEJ_02341 | 4.8e-110 | kdgK | 2.7.1.45 | G | pfkB family carbohydrate kinase | |
FEAFEJEJ_02342 | 4.2e-81 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
FEAFEJEJ_02343 | 1.4e-39 | |||||
FEAFEJEJ_02344 | 8e-129 | IQ | reductase | |||
FEAFEJEJ_02345 | 6.4e-241 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
FEAFEJEJ_02346 | 8.2e-154 | S | Uncharacterised protein, DegV family COG1307 | |||
FEAFEJEJ_02347 | 2.5e-269 | nox | C | NADH oxidase | ||
FEAFEJEJ_02348 | 2.3e-56 | trxA1 | O | Belongs to the thioredoxin family | ||
FEAFEJEJ_02349 | 1.3e-38 | yrkD | S | Metal-sensitive transcriptional repressor | ||
FEAFEJEJ_02350 | 3.5e-59 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
FEAFEJEJ_02351 | 5.4e-59 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
FEAFEJEJ_02352 | 4.2e-150 | M1-1017 | ||||
FEAFEJEJ_02353 | 3.9e-164 | I | Carboxylesterase family | |||
FEAFEJEJ_02354 | 3.3e-88 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
FEAFEJEJ_02355 | 4.5e-165 | |||||
FEAFEJEJ_02356 | 2.5e-250 | pts14C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
FEAFEJEJ_02357 | 2.1e-168 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
FEAFEJEJ_02358 | 1e-156 | lysR5 | K | LysR substrate binding domain | ||
FEAFEJEJ_02359 | 9e-145 | yxaA | S | membrane transporter protein | ||
FEAFEJEJ_02360 | 5.4e-57 | ywjH | S | Protein of unknown function (DUF1634) | ||
FEAFEJEJ_02361 | 7.8e-140 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
FEAFEJEJ_02362 | 6.8e-226 | mdtG | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02363 | 8.9e-18 | 2.7.6.5 | S | RelA SpoT domain protein | ||
FEAFEJEJ_02364 | 6.6e-53 | 2.7.6.5 | S | RelA SpoT domain protein | ||
FEAFEJEJ_02365 | 8.1e-28 | S | Protein of unknown function (DUF2929) | |||
FEAFEJEJ_02366 | 5.5e-169 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
FEAFEJEJ_02368 | 0.0 | S | membrane | |||
FEAFEJEJ_02369 | 1.4e-122 | K | cheY-homologous receiver domain | |||
FEAFEJEJ_02370 | 1.1e-234 | ciaH | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
FEAFEJEJ_02371 | 1.8e-181 | malR | K | Transcriptional regulator, LacI family | ||
FEAFEJEJ_02372 | 1.3e-254 | malT | G | Major Facilitator | ||
FEAFEJEJ_02373 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
FEAFEJEJ_02374 | 2.4e-77 | |||||
FEAFEJEJ_02375 | 6e-42 | 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 | ||
FEAFEJEJ_02376 | 2.7e-151 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
FEAFEJEJ_02377 | 2.8e-159 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
FEAFEJEJ_02378 | 2.8e-151 | 3.1.3.102, 3.1.3.104 | S | Sucrose-6F-phosphate phosphohydrolase | ||
FEAFEJEJ_02379 | 4.6e-64 | K | MarR family | |||
FEAFEJEJ_02380 | 5.4e-248 | yclG | M | Parallel beta-helix repeats | ||
FEAFEJEJ_02381 | 2.7e-73 | spx4 | 1.20.4.1 | P | ArsC family | |
FEAFEJEJ_02382 | 5.9e-143 | iap | CBM50 | M | NlpC/P60 family | |
FEAFEJEJ_02383 | 1.7e-47 | K | acetyltransferase | |||
FEAFEJEJ_02384 | 2.4e-31 | K | acetyltransferase | |||
FEAFEJEJ_02385 | 1.7e-08 | E | dipeptidase activity | |||
FEAFEJEJ_02386 | 3.8e-276 | E | dipeptidase activity | |||
FEAFEJEJ_02387 | 1.6e-230 | L | Transposase | |||
FEAFEJEJ_02388 | 3e-96 | S | membrane transporter protein | |||
FEAFEJEJ_02389 | 1.3e-19 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
FEAFEJEJ_02390 | 3.4e-77 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
FEAFEJEJ_02391 | 1.9e-133 | IQ | Dehydrogenases with different specificities (related to short-chain alcohol dehydrogenases) | |||
FEAFEJEJ_02392 | 1.6e-152 | 1.6.5.2 | GM | NmrA-like family | ||
FEAFEJEJ_02393 | 1.4e-72 | K | Transcriptional regulator | |||
FEAFEJEJ_02394 | 0.0 | 2.7.8.12 | M | glycerophosphotransferase | ||
FEAFEJEJ_02395 | 6.2e-73 | |||||
FEAFEJEJ_02397 | 7e-175 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02398 | 9.4e-101 | tnpR1 | L | Resolvase, N terminal domain | ||
FEAFEJEJ_02399 | 0.0 | kup | P | Transport of potassium into the cell | ||
FEAFEJEJ_02400 | 5e-64 | KT | Transcriptional regulatory protein, C terminal | |||
FEAFEJEJ_02401 | 3.8e-181 | T | PhoQ Sensor | |||
FEAFEJEJ_02402 | 2.3e-38 | kdpC | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit acts as a catalytic chaperone that increases the ATP- binding affinity of the ATP-hydrolyzing subunit KdpB by the formation of a transient KdpB KdpC ATP ternary complex | |
FEAFEJEJ_02403 | 1.5e-254 | kdpB | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system | |
FEAFEJEJ_02404 | 6e-175 | kdpA | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit binds and transports the potassium across the cytoplasmic membrane | |
FEAFEJEJ_02405 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02406 | 6.2e-138 | S | Protein of unknown function DUF262 | |||
FEAFEJEJ_02407 | 1e-75 | L | Transposase DDE domain | |||
FEAFEJEJ_02408 | 5.1e-68 | L | Putative transposase of IS4/5 family (DUF4096) | |||
FEAFEJEJ_02409 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
FEAFEJEJ_02411 | 0.0 | L | MobA MobL family protein | |||
FEAFEJEJ_02412 | 2.1e-26 | |||||
FEAFEJEJ_02413 | 3.4e-40 | |||||
FEAFEJEJ_02414 | 2.2e-193 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02415 | 5.8e-81 | |||||
FEAFEJEJ_02416 | 8.7e-44 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
FEAFEJEJ_02418 | 8.1e-119 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
FEAFEJEJ_02419 | 1.7e-22 | S | Family of unknown function (DUF5388) | |||
FEAFEJEJ_02420 | 1.2e-32 | |||||
FEAFEJEJ_02421 | 3.7e-176 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02422 | 4.1e-33 | pemK | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | ||
FEAFEJEJ_02423 | 4.8e-44 | T | Antidote-toxin recognition MazE, bacterial antitoxin | |||
FEAFEJEJ_02424 | 3.7e-105 | L | Integrase | |||
FEAFEJEJ_02425 | 3.5e-28 | |||||
FEAFEJEJ_02426 | 6.4e-176 | L | Initiator Replication protein | |||
FEAFEJEJ_02427 | 1.7e-73 | S | Protein of unknown function, DUF536 | |||
FEAFEJEJ_02428 | 2.2e-32 | |||||
FEAFEJEJ_02429 | 3.7e-60 | |||||
FEAFEJEJ_02430 | 4.6e-40 | |||||
FEAFEJEJ_02431 | 6.2e-137 | K | Helix-turn-helix domain | |||
FEAFEJEJ_02432 | 3.7e-176 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02433 | 2e-78 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
FEAFEJEJ_02434 | 1.4e-56 | K | Transcriptional regulator | |||
FEAFEJEJ_02435 | 3.2e-250 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
FEAFEJEJ_02436 | 4.5e-105 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
FEAFEJEJ_02437 | 2.2e-248 | L | Transposase | |||
FEAFEJEJ_02438 | 4.4e-181 | iolT | EGP | Major facilitator Superfamily | ||
FEAFEJEJ_02439 | 5.2e-18 | S | PFAM Archaeal ATPase | |||
FEAFEJEJ_02440 | 6.9e-231 | 1.7.1.15 | S | Pyridine nucleotide-disulphide oxidoreductase | ||
FEAFEJEJ_02441 | 2.2e-96 | yhiD | S | MgtC family | ||
FEAFEJEJ_02442 | 1.2e-51 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
FEAFEJEJ_02443 | 1.7e-54 | tnp2PF3 | L | Transposase DDE domain | ||
FEAFEJEJ_02444 | 1.4e-164 | corA | P | CorA-like Mg2+ transporter protein | ||
FEAFEJEJ_02445 | 3.5e-174 | L | Integrase core domain | |||
FEAFEJEJ_02446 | 7.9e-09 | zntR | K | helix_turn_helix, mercury resistance | ||
FEAFEJEJ_02448 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02450 | 6.6e-16 | S | peptidoglycan catabolic process | |||
FEAFEJEJ_02454 | 7.6e-66 | L | Transposase IS200 like | |||
FEAFEJEJ_02455 | 5.6e-174 | L | transposase, IS605 OrfB family | |||
FEAFEJEJ_02457 | 1.2e-08 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
FEAFEJEJ_02461 | 3.2e-59 | |||||
FEAFEJEJ_02463 | 1.4e-179 | gpG | ||||
FEAFEJEJ_02464 | 3.4e-43 | S | Domain of unknown function (DUF4355) | |||
FEAFEJEJ_02465 | 5.7e-76 | S | Phage Mu protein F like protein | |||
FEAFEJEJ_02466 | 1.1e-261 | S | Phage portal protein, SPP1 Gp6-like | |||
FEAFEJEJ_02468 | 5.5e-157 | ps334 | S | Terminase-like family | ||
FEAFEJEJ_02469 | 3.1e-72 | L | Terminase small subunit | |||
FEAFEJEJ_02470 | 1.8e-17 | S | Protein of unknown function (DUF2829) | |||
FEAFEJEJ_02472 | 9.2e-34 | S | Transcriptional regulator, RinA family | |||
FEAFEJEJ_02477 | 3.2e-72 | pi346 | L | IstB-like ATP binding protein | ||
FEAFEJEJ_02478 | 1.1e-58 | ybl78 | L | Conserved phage C-terminus (Phg_2220_C) | ||
FEAFEJEJ_02479 | 2.8e-86 | S | Putative HNHc nuclease | |||
FEAFEJEJ_02480 | 5.2e-56 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
FEAFEJEJ_02481 | 2.7e-128 | |||||
FEAFEJEJ_02482 | 3.5e-30 | S | ERF superfamily | |||
FEAFEJEJ_02489 | 5.7e-100 | S | DNA binding | |||
FEAFEJEJ_02490 | 4.6e-10 | K | Helix-turn-helix XRE-family like proteins | |||
FEAFEJEJ_02491 | 8.7e-40 | XK27_10050 | K | Peptidase S24-like | ||
FEAFEJEJ_02492 | 6.6e-13 | S | Protein of unknown function (DUF805) | |||
FEAFEJEJ_02493 | 1.2e-55 | |||||
FEAFEJEJ_02494 | 2.2e-48 | |||||
FEAFEJEJ_02495 | 6.7e-44 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase | |
FEAFEJEJ_02497 | 7.1e-56 | |||||
FEAFEJEJ_02499 | 1.3e-95 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
FEAFEJEJ_02500 | 1.4e-17 | |||||
FEAFEJEJ_02502 | 3.7e-87 | 3.2.1.17 | M | hydrolase, family 25 | ||
FEAFEJEJ_02503 | 4e-40 | |||||
FEAFEJEJ_02504 | 4.3e-51 | D | nuclear chromosome segregation | |||
FEAFEJEJ_02506 | 1.9e-180 | Z012_12235 | S | Baseplate J-like protein | ||
FEAFEJEJ_02508 | 6.3e-43 | |||||
FEAFEJEJ_02509 | 8.7e-133 | |||||
FEAFEJEJ_02510 | 2.4e-16 | |||||
FEAFEJEJ_02511 | 1.9e-60 | M | LysM domain | |||
FEAFEJEJ_02512 | 6.3e-37 | D | NLP P60 protein | |||
FEAFEJEJ_02513 | 0.0 | traE | U | type IV secretory pathway VirB4 | ||
FEAFEJEJ_02514 | 1.3e-217 | polC | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | S | WXG100 protein secretion system (Wss), protein YukC |
FEAFEJEJ_02515 | 1.5e-203 | M | CHAP domain | |||
FEAFEJEJ_02516 | 8.2e-87 | |||||
FEAFEJEJ_02517 | 9e-57 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
FEAFEJEJ_02518 | 6e-74 | |||||
FEAFEJEJ_02519 | 2.2e-263 | traK | U | COG3505 Type IV secretory pathway, VirD4 components | ||
FEAFEJEJ_02520 | 2.2e-55 | |||||
FEAFEJEJ_02521 | 7e-153 | |||||
FEAFEJEJ_02522 | 2.6e-65 | |||||
FEAFEJEJ_02523 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
FEAFEJEJ_02524 | 2.9e-29 | |||||
FEAFEJEJ_02525 | 1.6e-189 | L | Psort location Cytoplasmic, score | |||
FEAFEJEJ_02527 | 3.9e-19 | L | Transposase DDE domain | |||
FEAFEJEJ_02528 | 1.7e-49 | prrC | S | AAA domain | ||
FEAFEJEJ_02529 | 6.3e-107 | pstIR | 2.1.1.72, 3.1.21.4 | L | BsuBI/PstI restriction endonuclease C-terminus | |
FEAFEJEJ_02530 | 8e-144 | L | Eco57I restriction-modification methylase | |||
FEAFEJEJ_02531 | 3e-195 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02532 | 3.7e-176 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02533 | 3.1e-54 | L | recombinase activity | |||
FEAFEJEJ_02534 | 8.1e-49 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02535 | 6.4e-47 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02536 | 4.4e-121 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
FEAFEJEJ_02537 | 1.6e-244 | ugpB | G | Bacterial extracellular solute-binding protein | ||
FEAFEJEJ_02538 | 9.1e-150 | ugpE | G | ABC transporter permease | ||
FEAFEJEJ_02539 | 3.6e-166 | ugpA | U | Binding-protein-dependent transport system inner membrane component | ||
FEAFEJEJ_02540 | 2.5e-192 | ugpC | 3.6.3.20 | E | Belongs to the ABC transporter superfamily | |
FEAFEJEJ_02541 | 3.8e-79 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02542 | 2.2e-193 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02543 | 4.8e-84 | L | Resolvase, N terminal domain | |||
FEAFEJEJ_02544 | 5.6e-136 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
FEAFEJEJ_02545 | 2.2e-30 | |||||
FEAFEJEJ_02546 | 1.9e-115 | repA | S | Replication initiator protein A | ||
FEAFEJEJ_02547 | 8.6e-22 | |||||
FEAFEJEJ_02548 | 3.8e-131 | S | Fic/DOC family | |||
FEAFEJEJ_02549 | 5.1e-36 | |||||
FEAFEJEJ_02550 | 4.9e-22 | |||||
FEAFEJEJ_02551 | 0.0 | traA | L | MobA MobL family protein | ||
FEAFEJEJ_02552 | 4e-50 | |||||
FEAFEJEJ_02553 | 5.2e-102 | |||||
FEAFEJEJ_02554 | 1e-51 | S | Cag pathogenicity island, type IV secretory system | |||
FEAFEJEJ_02555 | 7.8e-37 | |||||
FEAFEJEJ_02556 | 3.1e-116 | |||||
FEAFEJEJ_02557 | 1.1e-128 | L | Psort location Cytoplasmic, score | |||
FEAFEJEJ_02558 | 4.1e-173 | prrC | S | AAA domain | ||
FEAFEJEJ_02559 | 3.4e-225 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
FEAFEJEJ_02560 | 3e-111 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
FEAFEJEJ_02561 | 1.3e-97 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
FEAFEJEJ_02562 | 3e-209 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
FEAFEJEJ_02563 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02564 | 1.2e-33 | recQ | 3.6.4.12 | L | PFAM DEAD DEAH box helicase domain protein | |
FEAFEJEJ_02565 | 9.5e-14 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_02566 | 1.4e-87 | L | Integrase | |||
FEAFEJEJ_02567 | 1.5e-36 | Q | ubiE/COQ5 methyltransferase family | |||
FEAFEJEJ_02568 | 1e-57 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
FEAFEJEJ_02569 | 1.2e-194 | O | Heat shock 70 kDa protein | |||
FEAFEJEJ_02570 | 7.2e-43 | |||||
FEAFEJEJ_02571 | 2.1e-53 | |||||
FEAFEJEJ_02572 | 1.3e-132 | repA | S | Replication initiator protein A | ||
FEAFEJEJ_02573 | 4e-41 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
FEAFEJEJ_02574 | 5.9e-28 | |||||
FEAFEJEJ_02575 | 1.6e-115 | S | protein conserved in bacteria | |||
FEAFEJEJ_02576 | 8.9e-41 | |||||
FEAFEJEJ_02577 | 5.5e-27 | |||||
FEAFEJEJ_02578 | 0.0 | traA | L | MobA MobL family protein | ||
FEAFEJEJ_02579 | 1.5e-49 | |||||
FEAFEJEJ_02580 | 1.4e-102 | |||||
FEAFEJEJ_02581 | 1e-51 | S | Cag pathogenicity island, type IV secretory system | |||
FEAFEJEJ_02582 | 1.3e-36 | |||||
FEAFEJEJ_02583 | 6.2e-117 | |||||
FEAFEJEJ_02584 | 0.0 | U | AAA-like domain | |||
FEAFEJEJ_02585 | 2.1e-231 | polC | 2.4.1.129, 2.7.7.7, 3.4.16.4 | GT51 | S | WXG100 protein secretion system (Wss), protein YukC |
FEAFEJEJ_02586 | 1.6e-208 | M | CHAP domain | |||
FEAFEJEJ_02587 | 1.5e-88 | |||||
FEAFEJEJ_02588 | 1.3e-64 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
FEAFEJEJ_02589 | 1e-81 | |||||
FEAFEJEJ_02590 | 4.7e-269 | traK | U | COG3505 Type IV secretory pathway, VirD4 components | ||
FEAFEJEJ_02591 | 1.4e-60 | |||||
FEAFEJEJ_02592 | 3.5e-152 | |||||
FEAFEJEJ_02593 | 4e-66 | |||||
FEAFEJEJ_02594 | 0.0 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
FEAFEJEJ_02595 | 3.8e-31 | |||||
FEAFEJEJ_02596 | 5.5e-45 | U | Relaxase/Mobilisation nuclease domain | |||
FEAFEJEJ_02597 | 7.3e-172 | L | Initiator Replication protein | |||
FEAFEJEJ_02598 | 1.3e-94 | |||||
FEAFEJEJ_02599 | 6.6e-88 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain protein | ||
FEAFEJEJ_02600 | 1.9e-138 | K | Helix-turn-helix domain | |||
FEAFEJEJ_02603 | 4.3e-62 | S | GIY-YIG catalytic domain | |||
FEAFEJEJ_02604 | 1.1e-59 | yafQ | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | ||
FEAFEJEJ_02605 | 3.9e-44 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
FEAFEJEJ_02606 | 1.3e-105 | L | Integrase | |||
FEAFEJEJ_02607 | 9.3e-44 | |||||
FEAFEJEJ_02609 | 4.4e-133 | L | PFAM transposase, IS4 family protein | |||
FEAFEJEJ_02611 | 1.1e-112 | IQ | KR domain | |||
FEAFEJEJ_02612 | 8e-197 | luxC | 1.2.1.50 | C | Acyl-CoA reductase (LuxC) | |
FEAFEJEJ_02613 | 1.4e-164 | luxE | 6.2.1.19 | H | Acyl-protein synthetase, LuxE | |
FEAFEJEJ_02614 | 1e-203 | F | Permease | |||
FEAFEJEJ_02617 | 3.4e-37 | K | sequence-specific DNA binding | |||
FEAFEJEJ_02618 | 3.7e-52 | S | Bacterial mobilisation protein (MobC) | |||
FEAFEJEJ_02619 | 8.4e-105 | repA | S | Replication initiator protein A | ||
FEAFEJEJ_02620 | 7.4e-43 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
FEAFEJEJ_02621 | 5.9e-28 | |||||
FEAFEJEJ_02622 | 3.1e-41 | |||||
FEAFEJEJ_02623 | 0.0 | L | MobA MobL family protein | |||
FEAFEJEJ_02624 | 7.7e-62 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
FEAFEJEJ_02625 | 0.0 | M | domain protein | |||
FEAFEJEJ_02626 | 2e-10 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
FEAFEJEJ_02627 | 3e-23 | K | DeoR C terminal sensor domain | |||
FEAFEJEJ_02628 | 2.3e-99 | tnpR | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | ||
FEAFEJEJ_02629 | 2.2e-193 | O | Heat shock 70 kDa protein | |||
FEAFEJEJ_02630 | 1.4e-41 | |||||
FEAFEJEJ_02631 | 5.7e-59 | |||||
FEAFEJEJ_02632 | 1.2e-41 | |||||
FEAFEJEJ_02633 | 3.8e-28 | uspA | T | Universal stress protein family | ||
FEAFEJEJ_02635 | 3.9e-44 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
FEAFEJEJ_02636 | 1.2e-81 | |||||
FEAFEJEJ_02637 | 5.4e-69 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02638 | 8.7e-113 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02639 | 1.1e-47 | |||||
FEAFEJEJ_02640 | 4.1e-175 | L | Transposase and inactivated derivatives, IS30 family | |||
FEAFEJEJ_02641 | 1.2e-23 | S | Family of unknown function (DUF5388) | |||
FEAFEJEJ_02642 | 1.6e-143 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
FEAFEJEJ_02643 | 3.2e-36 | 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 | |
FEAFEJEJ_02644 | 4.6e-35 | L | Transposase | |||
FEAFEJEJ_02645 | 1.9e-141 | L | Transposase | |||
FEAFEJEJ_02647 | 2.7e-174 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
FEAFEJEJ_02648 | 5.8e-11 | |||||
FEAFEJEJ_02651 | 1e-44 | ycnE | 3.1.1.29 | S | Antibiotic biosynthesis monooxygenase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)