ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AEOOMBIJ_00001 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
AEOOMBIJ_00002 | 4.5e-192 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
AEOOMBIJ_00003 | 5.6e-179 | S | PFAM Archaeal ATPase | |||
AEOOMBIJ_00004 | 2.4e-73 | S | cog cog1373 | |||
AEOOMBIJ_00005 | 6.1e-42 | ruvB | 3.6.4.12 | L | four-way junction helicase activity | |
AEOOMBIJ_00006 | 9.5e-38 | L | Protein of unknown function (DUF3991) | |||
AEOOMBIJ_00007 | 4.2e-112 | S | Fic/DOC family | |||
AEOOMBIJ_00008 | 1.7e-48 | E | Pfam:DUF955 | |||
AEOOMBIJ_00009 | 9.8e-24 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
AEOOMBIJ_00010 | 5.6e-18 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
AEOOMBIJ_00012 | 1.2e-134 | topA2 | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
AEOOMBIJ_00014 | 1.3e-24 | S | CAAX protease self-immunity | |||
AEOOMBIJ_00016 | 4.1e-34 | |||||
AEOOMBIJ_00017 | 1.3e-66 | doc | S | Fic/DOC family | ||
AEOOMBIJ_00019 | 8.7e-242 | V | N-6 DNA Methylase | |||
AEOOMBIJ_00020 | 3.3e-86 | bcgIB | 2.1.1.72, 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AEOOMBIJ_00021 | 1.6e-35 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
AEOOMBIJ_00022 | 5e-39 | relB | L | RelB antitoxin | ||
AEOOMBIJ_00024 | 3e-97 | D | VirC1 protein | |||
AEOOMBIJ_00025 | 2.7e-36 | yyaR | K | Acetyltransferase (GNAT) domain | ||
AEOOMBIJ_00026 | 3.2e-72 | 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 | ||
AEOOMBIJ_00027 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
AEOOMBIJ_00028 | 3e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
AEOOMBIJ_00029 | 1.1e-152 | 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 | |
AEOOMBIJ_00030 | 8.6e-199 | tnpB | L | Putative transposase DNA-binding domain | ||
AEOOMBIJ_00031 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
AEOOMBIJ_00032 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AEOOMBIJ_00033 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
AEOOMBIJ_00034 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
AEOOMBIJ_00035 | 5.3e-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 | ||
AEOOMBIJ_00036 | 4.6e-216 | ylbM | S | Belongs to the UPF0348 family | ||
AEOOMBIJ_00037 | 4.7e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
AEOOMBIJ_00038 | 1.2e-126 | K | response regulator | |||
AEOOMBIJ_00039 | 3.4e-278 | arlS | 2.7.13.3 | T | Histidine kinase | |
AEOOMBIJ_00040 | 1e-12 | |||||
AEOOMBIJ_00041 | 1.5e-97 | S | CAAX protease self-immunity | |||
AEOOMBIJ_00042 | 6.1e-224 | S | SLAP domain | |||
AEOOMBIJ_00043 | 5.7e-83 | S | Aminoacyl-tRNA editing domain | |||
AEOOMBIJ_00044 | 2.4e-162 | 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 | ||
AEOOMBIJ_00045 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
AEOOMBIJ_00046 | 2.2e-134 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AEOOMBIJ_00047 | 4.5e-58 | yodB | K | Transcriptional regulator, HxlR family | ||
AEOOMBIJ_00049 | 8.3e-24 | papP | P | ABC transporter, permease protein | ||
AEOOMBIJ_00050 | 7.5e-103 | G | Phosphoglycerate mutase family | |||
AEOOMBIJ_00051 | 7.8e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AEOOMBIJ_00053 | 1.2e-222 | patA | 2.6.1.1 | E | Aminotransferase | |
AEOOMBIJ_00054 | 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) | |
AEOOMBIJ_00055 | 5.8e-244 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AEOOMBIJ_00056 | 6e-76 | 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 | ||
AEOOMBIJ_00057 | 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 | |
AEOOMBIJ_00058 | 8.5e-60 | |||||
AEOOMBIJ_00059 | 6.5e-176 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AEOOMBIJ_00060 | 8.2e-85 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AEOOMBIJ_00061 | 5.9e-37 | M | domain protein | |||
AEOOMBIJ_00062 | 5.2e-68 | L | haloacid dehalogenase-like hydrolase | |||
AEOOMBIJ_00063 | 4.9e-123 | 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 | |
AEOOMBIJ_00064 | 7.2e-129 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
AEOOMBIJ_00065 | 2.8e-90 | ulaD | 4.1.1.85, 4.1.2.43 | G | Orotidine 5'-phosphate decarboxylase / HUMPS family | |
AEOOMBIJ_00066 | 4.1e-31 | sgaB | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AEOOMBIJ_00067 | 5.3e-233 | ulaA | S | PTS system sugar-specific permease component | ||
AEOOMBIJ_00068 | 1.5e-61 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
AEOOMBIJ_00069 | 8.1e-175 | ulaG | S | Beta-lactamase superfamily domain | ||
AEOOMBIJ_00070 | 2.2e-78 | S | helix_turn_helix, Deoxyribose operon repressor | |||
AEOOMBIJ_00071 | 3.3e-140 | repB | EP | Plasmid replication protein | ||
AEOOMBIJ_00072 | 2.2e-22 | |||||
AEOOMBIJ_00073 | 8.8e-58 | S | Peptidase propeptide and YPEB domain | |||
AEOOMBIJ_00074 | 1.3e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
AEOOMBIJ_00075 | 2.5e-169 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
AEOOMBIJ_00076 | 7.1e-98 | E | GDSL-like Lipase/Acylhydrolase | |||
AEOOMBIJ_00077 | 7.5e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
AEOOMBIJ_00078 | 1.6e-143 | aatB | ET | ABC transporter substrate-binding protein | ||
AEOOMBIJ_00079 | 1e-105 | glnQ | 3.6.3.21 | E | ABC transporter | |
AEOOMBIJ_00080 | 1.5e-107 | glnP | P | ABC transporter permease | ||
AEOOMBIJ_00081 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
AEOOMBIJ_00082 | 5.6e-118 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
AEOOMBIJ_00083 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
AEOOMBIJ_00084 | 3.7e-243 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
AEOOMBIJ_00085 | 2.5e-47 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AEOOMBIJ_00086 | 6.9e-116 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
AEOOMBIJ_00087 | 9.7e-52 | S | Iron-sulfur cluster assembly protein | |||
AEOOMBIJ_00088 | 3.8e-154 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
AEOOMBIJ_00089 | 1.3e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
AEOOMBIJ_00090 | 5.2e-08 | |||||
AEOOMBIJ_00091 | 3e-89 | ntd | 2.4.2.6 | F | Nucleoside | |
AEOOMBIJ_00092 | 8.6e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
AEOOMBIJ_00093 | 7.5e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
AEOOMBIJ_00094 | 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 | ||
AEOOMBIJ_00095 | 3.5e-32 | ykzG | S | Belongs to the UPF0356 family | ||
AEOOMBIJ_00096 | 8.9e-101 | 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 | |
AEOOMBIJ_00097 | 0.0 | typA | T | GTP-binding protein TypA | ||
AEOOMBIJ_00098 | 5.9e-211 | ftsW | D | Belongs to the SEDS family | ||
AEOOMBIJ_00099 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AEOOMBIJ_00100 | 4.5e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
AEOOMBIJ_00101 | 3.6e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
AEOOMBIJ_00102 | 2.4e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
AEOOMBIJ_00103 | 3.1e-79 | comEA | L | Competence protein ComEA | ||
AEOOMBIJ_00104 | 0.0 | comEC | S | Competence protein ComEC | ||
AEOOMBIJ_00105 | 2.6e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
AEOOMBIJ_00106 | 2.6e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
AEOOMBIJ_00107 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
AEOOMBIJ_00108 | 3e-310 | 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 | ||
AEOOMBIJ_00109 | 1.3e-148 | |||||
AEOOMBIJ_00110 | 1.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AEOOMBIJ_00111 | 5.8e-215 | 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 | ||
AEOOMBIJ_00112 | 2e-233 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
AEOOMBIJ_00113 | 1.4e-104 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
AEOOMBIJ_00114 | 7.8e-39 | yjeM | E | Amino Acid | ||
AEOOMBIJ_00115 | 3.4e-175 | yjeM | E | Amino Acid | ||
AEOOMBIJ_00116 | 2.3e-192 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
AEOOMBIJ_00117 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AEOOMBIJ_00118 | 1.8e-245 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AEOOMBIJ_00119 | 2.8e-75 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
AEOOMBIJ_00120 | 2e-219 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AEOOMBIJ_00121 | 9.8e-177 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AEOOMBIJ_00122 | 7e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
AEOOMBIJ_00123 | 2.7e-216 | aspC | 2.6.1.1 | E | Aminotransferase | |
AEOOMBIJ_00124 | 2.6e-197 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
AEOOMBIJ_00125 | 2.1e-194 | pbpX1 | V | Beta-lactamase | ||
AEOOMBIJ_00126 | 1.2e-299 | I | Protein of unknown function (DUF2974) | |||
AEOOMBIJ_00127 | 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 | ||
AEOOMBIJ_00128 | 1.7e-243 | 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 | ||
AEOOMBIJ_00129 | 2.2e-292 | I | Acyltransferase | |||
AEOOMBIJ_00130 | 5.4e-175 | 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 | |
AEOOMBIJ_00131 | 5.1e-142 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AEOOMBIJ_00132 | 2.9e-117 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
AEOOMBIJ_00133 | 1e-79 | S | AAA domain | |||
AEOOMBIJ_00134 | 3.3e-61 | 3.6.1.55 | F | NUDIX domain | ||
AEOOMBIJ_00135 | 3.6e-88 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
AEOOMBIJ_00136 | 7.7e-10 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
AEOOMBIJ_00137 | 2.9e-109 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
AEOOMBIJ_00138 | 1.7e-36 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
AEOOMBIJ_00139 | 1.1e-59 | axe1 | 3.1.1.41 | Q | Acetyl xylan esterase (AXE1) | |
AEOOMBIJ_00140 | 1e-220 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
AEOOMBIJ_00141 | 1.9e-121 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
AEOOMBIJ_00142 | 2.3e-56 | G | Xylose isomerase domain protein TIM barrel | |||
AEOOMBIJ_00143 | 8.4e-90 | nanK | GK | ROK family | ||
AEOOMBIJ_00144 | 2.9e-122 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
AEOOMBIJ_00145 | 3.7e-66 | K | Helix-turn-helix domain, rpiR family | |||
AEOOMBIJ_00146 | 7.1e-263 | E | ABC transporter, substratebinding protein | |||
AEOOMBIJ_00147 | 9.1e-10 | K | peptidyl-tyrosine sulfation | |||
AEOOMBIJ_00149 | 1.2e-128 | S | interspecies interaction between organisms | |||
AEOOMBIJ_00150 | 2.7e-34 | |||||
AEOOMBIJ_00153 | 1.9e-21 | |||||
AEOOMBIJ_00154 | 1.7e-147 | |||||
AEOOMBIJ_00155 | 1.5e-169 | |||||
AEOOMBIJ_00156 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AEOOMBIJ_00157 | 7.8e-222 | ynbB | 4.4.1.1 | P | aluminum resistance | |
AEOOMBIJ_00158 | 1e-168 | 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) | |
AEOOMBIJ_00159 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
AEOOMBIJ_00160 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
AEOOMBIJ_00161 | 3.1e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
AEOOMBIJ_00162 | 2.1e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AEOOMBIJ_00163 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AEOOMBIJ_00164 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AEOOMBIJ_00165 | 0.0 | S | membrane | |||
AEOOMBIJ_00166 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
AEOOMBIJ_00167 | 1.3e-38 | S | RelB antitoxin | |||
AEOOMBIJ_00168 | 3.4e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
AEOOMBIJ_00169 | 6.7e-44 | 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 | ||
AEOOMBIJ_00170 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
AEOOMBIJ_00171 | 9.5e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AEOOMBIJ_00172 | 8.7e-159 | isdE | P | Periplasmic binding protein | ||
AEOOMBIJ_00173 | 6.3e-123 | M | Iron Transport-associated domain | |||
AEOOMBIJ_00174 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
AEOOMBIJ_00175 | 8.4e-89 | |||||
AEOOMBIJ_00176 | 6.4e-113 | S | SLAP domain | |||
AEOOMBIJ_00177 | 1.2e-51 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
AEOOMBIJ_00178 | 7e-24 | K | response regulator | |||
AEOOMBIJ_00179 | 1.1e-103 | sptS | 2.7.13.3 | T | Histidine kinase | |
AEOOMBIJ_00180 | 2.6e-103 | sptS | 2.7.13.3 | T | Histidine kinase | |
AEOOMBIJ_00181 | 1.4e-207 | EGP | Major facilitator Superfamily | |||
AEOOMBIJ_00182 | 2.3e-69 | O | OsmC-like protein | |||
AEOOMBIJ_00183 | 2.2e-85 | S | Protein of unknown function (DUF805) | |||
AEOOMBIJ_00184 | 2.5e-71 | |||||
AEOOMBIJ_00185 | 3.1e-93 | |||||
AEOOMBIJ_00186 | 9.9e-180 | |||||
AEOOMBIJ_00187 | 5.8e-83 | S | Fic/DOC family | |||
AEOOMBIJ_00188 | 3.3e-275 | yjeM | E | Amino Acid | ||
AEOOMBIJ_00189 | 1.1e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AEOOMBIJ_00190 | 5.4e-113 | |||||
AEOOMBIJ_00191 | 1.7e-139 | |||||
AEOOMBIJ_00192 | 6.9e-100 | V | ATPases associated with a variety of cellular activities | |||
AEOOMBIJ_00193 | 3.7e-146 | ykuT | M | mechanosensitive ion channel | ||
AEOOMBIJ_00194 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
AEOOMBIJ_00195 | 1.3e-36 | |||||
AEOOMBIJ_00196 | 7e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AEOOMBIJ_00197 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
AEOOMBIJ_00198 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AEOOMBIJ_00199 | 4.3e-55 | |||||
AEOOMBIJ_00200 | 5.8e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
AEOOMBIJ_00201 | 2.1e-92 | yutD | S | Protein of unknown function (DUF1027) | ||
AEOOMBIJ_00202 | 3.4e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
AEOOMBIJ_00203 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
AEOOMBIJ_00204 | 6.8e-116 | dedA | S | SNARE-like domain protein | ||
AEOOMBIJ_00205 | 7.5e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
AEOOMBIJ_00206 | 7e-23 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AEOOMBIJ_00207 | 3.7e-130 | ybbH_2 | K | rpiR family | ||
AEOOMBIJ_00208 | 3.4e-195 | S | Bacterial protein of unknown function (DUF871) | |||
AEOOMBIJ_00209 | 4.1e-214 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
AEOOMBIJ_00210 | 1.8e-119 | S | Putative esterase | |||
AEOOMBIJ_00211 | 1.6e-120 | 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 | |
AEOOMBIJ_00212 | 1.3e-79 | ybbH_2 | K | Helix-turn-helix domain, rpiR family | ||
AEOOMBIJ_00213 | 8.5e-260 | qacA | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_00214 | 1.7e-221 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
AEOOMBIJ_00217 | 6.2e-165 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
AEOOMBIJ_00219 | 5.6e-08 | M | Host cell surface-exposed lipoprotein | |||
AEOOMBIJ_00220 | 2.4e-07 | S | Pfam:DUF955 | |||
AEOOMBIJ_00221 | 8.8e-22 | K | Helix-turn-helix XRE-family like proteins | |||
AEOOMBIJ_00222 | 1.4e-17 | K | Helix-turn-helix XRE-family like proteins | |||
AEOOMBIJ_00223 | 1.2e-210 | S | Bacterial protein of unknown function (DUF871) | |||
AEOOMBIJ_00224 | 2.3e-43 | ybhL | S | Belongs to the BI1 family | ||
AEOOMBIJ_00225 | 5.5e-148 | S | cog cog1373 | |||
AEOOMBIJ_00226 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
AEOOMBIJ_00227 | 2e-91 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
AEOOMBIJ_00228 | 1.9e-259 | emrY | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_00233 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
AEOOMBIJ_00234 | 4.9e-254 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AEOOMBIJ_00235 | 6.3e-201 | pbpX | V | Beta-lactamase | ||
AEOOMBIJ_00236 | 2.8e-244 | nhaC | C | Na H antiporter NhaC | ||
AEOOMBIJ_00237 | 1.4e-147 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
AEOOMBIJ_00238 | 2.6e-57 | |||||
AEOOMBIJ_00239 | 4.3e-108 | ybhL | S | Belongs to the BI1 family | ||
AEOOMBIJ_00240 | 2.7e-171 | yegS | 2.7.1.107 | G | Lipid kinase | |
AEOOMBIJ_00241 | 2.7e-274 | 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) | |
AEOOMBIJ_00242 | 2.9e-268 | 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) | |
AEOOMBIJ_00243 | 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) | |
AEOOMBIJ_00244 | 5.8e-203 | camS | S | sex pheromone | ||
AEOOMBIJ_00245 | 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 | |
AEOOMBIJ_00246 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
AEOOMBIJ_00247 | 5.2e-84 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
AEOOMBIJ_00249 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
AEOOMBIJ_00250 | 7.7e-134 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
AEOOMBIJ_00251 | 3e-257 | epsU | S | Polysaccharide biosynthesis protein | ||
AEOOMBIJ_00252 | 7e-225 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
AEOOMBIJ_00253 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
AEOOMBIJ_00254 | 1.4e-204 | tnpB | L | Putative transposase DNA-binding domain | ||
AEOOMBIJ_00255 | 1.2e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
AEOOMBIJ_00256 | 2.4e-286 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
AEOOMBIJ_00257 | 1.7e-204 | csaB | M | Glycosyl transferases group 1 | ||
AEOOMBIJ_00258 | 2.1e-134 | 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 |
AEOOMBIJ_00259 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
AEOOMBIJ_00260 | 4.6e-123 | gntR1 | K | UTRA | ||
AEOOMBIJ_00261 | 3.3e-179 | |||||
AEOOMBIJ_00262 | 3.4e-45 | oppA2 | E | ABC transporter, substratebinding protein | ||
AEOOMBIJ_00263 | 4.4e-239 | oppA2 | E | ABC transporter, substratebinding protein | ||
AEOOMBIJ_00266 | 3.2e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
AEOOMBIJ_00267 | 6.6e-11 | |||||
AEOOMBIJ_00268 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
AEOOMBIJ_00269 | 6.7e-228 | slpX | S | SLAP domain | ||
AEOOMBIJ_00270 | 4.4e-144 | K | SIS domain | |||
AEOOMBIJ_00271 | 8.1e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
AEOOMBIJ_00272 | 2.7e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
AEOOMBIJ_00273 | 6.5e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
AEOOMBIJ_00275 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
AEOOMBIJ_00277 | 1.2e-115 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
AEOOMBIJ_00278 | 6.6e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
AEOOMBIJ_00279 | 2.6e-89 | G | Histidine phosphatase superfamily (branch 1) | |||
AEOOMBIJ_00280 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
AEOOMBIJ_00281 | 4.7e-159 | D | nuclear chromosome segregation | |||
AEOOMBIJ_00282 | 5.8e-160 | V | ABC transporter transmembrane region | |||
AEOOMBIJ_00283 | 7e-68 | V | ABC transporter transmembrane region | |||
AEOOMBIJ_00284 | 3.8e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
AEOOMBIJ_00285 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
AEOOMBIJ_00286 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
AEOOMBIJ_00287 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
AEOOMBIJ_00288 | 5.2e-187 | T | GHKL domain | |||
AEOOMBIJ_00289 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
AEOOMBIJ_00290 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
AEOOMBIJ_00291 | 2.9e-277 | V | ABC transporter transmembrane region | |||
AEOOMBIJ_00292 | 0.0 | fhaB | M | Rib/alpha-like repeat | ||
AEOOMBIJ_00293 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
AEOOMBIJ_00294 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
AEOOMBIJ_00295 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
AEOOMBIJ_00296 | 9e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
AEOOMBIJ_00297 | 6.8e-209 | msmX | P | Belongs to the ABC transporter superfamily | ||
AEOOMBIJ_00298 | 5e-213 | malE | G | Bacterial extracellular solute-binding protein | ||
AEOOMBIJ_00299 | 1.1e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
AEOOMBIJ_00300 | 3.3e-147 | malG | P | ABC transporter permease | ||
AEOOMBIJ_00301 | 4.3e-67 | K | Helix-turn-helix XRE-family like proteins | |||
AEOOMBIJ_00304 | 4.8e-28 | |||||
AEOOMBIJ_00305 | 4.1e-141 | aroD | S | Alpha/beta hydrolase family | ||
AEOOMBIJ_00306 | 2.2e-142 | S | Belongs to the UPF0246 family | |||
AEOOMBIJ_00307 | 1.2e-227 | 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 | |
AEOOMBIJ_00308 | 8.7e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
AEOOMBIJ_00309 | 3.2e-139 | 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 | |
AEOOMBIJ_00311 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein | |||
AEOOMBIJ_00312 | 3.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
AEOOMBIJ_00313 | 2e-52 | yaaQ | S | Cyclic-di-AMP receptor | ||
AEOOMBIJ_00314 | 6.3e-154 | holB | 2.7.7.7 | L | DNA polymerase III | |
AEOOMBIJ_00315 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
AEOOMBIJ_00316 | 5.1e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
AEOOMBIJ_00317 | 1.4e-130 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
AEOOMBIJ_00318 | 2.2e-85 | S | ECF transporter, substrate-specific component | |||
AEOOMBIJ_00319 | 2.4e-133 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
AEOOMBIJ_00320 | 7.4e-97 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
AEOOMBIJ_00321 | 4.5e-194 | 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 | |
AEOOMBIJ_00322 | 1.9e-245 | L | Transposase IS66 family | |||
AEOOMBIJ_00323 | 8.7e-34 | S | Transposase C of IS166 homeodomain | |||
AEOOMBIJ_00324 | 9.3e-64 | L | PFAM IS66 Orf2 family protein | |||
AEOOMBIJ_00325 | 7.7e-22 | |||||
AEOOMBIJ_00326 | 7e-43 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
AEOOMBIJ_00327 | 6.6e-182 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
AEOOMBIJ_00328 | 3.4e-284 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
AEOOMBIJ_00329 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00330 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
AEOOMBIJ_00331 | 2.1e-135 | UW | LPXTG-motif cell wall anchor domain protein | |||
AEOOMBIJ_00332 | 1.3e-161 | UW | LPXTG-motif cell wall anchor domain protein | |||
AEOOMBIJ_00333 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
AEOOMBIJ_00334 | 9.1e-10 | UW | LPXTG-motif cell wall anchor domain protein | |||
AEOOMBIJ_00335 | 1.3e-248 | 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) | |
AEOOMBIJ_00336 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
AEOOMBIJ_00337 | 1.4e-110 | yjbF | S | SNARE associated Golgi protein | ||
AEOOMBIJ_00338 | 3.8e-115 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AEOOMBIJ_00339 | 7.2e-183 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
AEOOMBIJ_00340 | 4.3e-52 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
AEOOMBIJ_00341 | 4.1e-156 | crtI | 1.3.99.23, 5.2.1.13 | Q | HI0933-like protein | |
AEOOMBIJ_00342 | 2.6e-65 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
AEOOMBIJ_00343 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AEOOMBIJ_00344 | 1.5e-102 | srtA | 3.4.22.70 | M | sortase family | |
AEOOMBIJ_00345 | 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 | ||
AEOOMBIJ_00346 | 2.2e-202 | 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 | ||
AEOOMBIJ_00347 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
AEOOMBIJ_00348 | 8e-68 | 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 | ||
AEOOMBIJ_00349 | 4.9e-193 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
AEOOMBIJ_00350 | 3.2e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AEOOMBIJ_00351 | 1.6e-155 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
AEOOMBIJ_00352 | 1.1e-59 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
AEOOMBIJ_00353 | 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 | ||
AEOOMBIJ_00354 | 3.2e-47 | rplGA | J | ribosomal protein | ||
AEOOMBIJ_00355 | 8.8e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
AEOOMBIJ_00356 | 1.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
AEOOMBIJ_00357 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
AEOOMBIJ_00358 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AEOOMBIJ_00359 | 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 | |
AEOOMBIJ_00360 | 5.7e-196 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
AEOOMBIJ_00361 | 8.4e-140 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
AEOOMBIJ_00362 | 1.3e-136 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
AEOOMBIJ_00363 | 5.3e-93 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
AEOOMBIJ_00364 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
AEOOMBIJ_00365 | 3.1e-184 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
AEOOMBIJ_00366 | 3.7e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
AEOOMBIJ_00367 | 3e-195 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
AEOOMBIJ_00368 | 2.9e-116 | plsC | 2.3.1.51 | I | Acyltransferase | |
AEOOMBIJ_00369 | 3.9e-223 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
AEOOMBIJ_00370 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AEOOMBIJ_00371 | 0.0 | mdlB | V | ABC transporter | ||
AEOOMBIJ_00372 | 0.0 | mdlA | V | ABC transporter | ||
AEOOMBIJ_00373 | 5.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
AEOOMBIJ_00374 | 3e-38 | ynzC | S | UPF0291 protein | ||
AEOOMBIJ_00375 | 2e-112 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
AEOOMBIJ_00376 | 9.8e-146 | E | GDSL-like Lipase/Acylhydrolase family | |||
AEOOMBIJ_00377 | 5.4e-121 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
AEOOMBIJ_00378 | 4.6e-213 | S | SLAP domain | |||
AEOOMBIJ_00379 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
AEOOMBIJ_00380 | 3.2e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AEOOMBIJ_00381 | 3.4e-94 | 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 | ||
AEOOMBIJ_00382 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
AEOOMBIJ_00383 | 4.9e-228 | 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 | |
AEOOMBIJ_00384 | 6e-55 | 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 | ||
AEOOMBIJ_00385 | 2.7e-258 | yfnA | E | amino acid | ||
AEOOMBIJ_00386 | 0.0 | V | FtsX-like permease family | |||
AEOOMBIJ_00387 | 4.1e-133 | cysA | V | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00388 | 3.4e-23 | |||||
AEOOMBIJ_00390 | 2.5e-288 | pipD | E | Dipeptidase | ||
AEOOMBIJ_00391 | 3.6e-161 | 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) | ||
AEOOMBIJ_00392 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
AEOOMBIJ_00393 | 1.9e-124 | 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 | |
AEOOMBIJ_00394 | 2.1e-308 | oppA | E | ABC transporter substrate-binding protein | ||
AEOOMBIJ_00395 | 3.1e-240 | oppA | E | ABC transporter substrate-binding protein | ||
AEOOMBIJ_00396 | 3.9e-31 | S | Domain of unknown function DUF1829 | |||
AEOOMBIJ_00397 | 1.1e-265 | |||||
AEOOMBIJ_00398 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
AEOOMBIJ_00399 | 4.3e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AEOOMBIJ_00400 | 3.9e-25 | |||||
AEOOMBIJ_00401 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
AEOOMBIJ_00402 | 5.7e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00403 | 6.5e-221 | ecsB | U | ABC transporter | ||
AEOOMBIJ_00404 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
AEOOMBIJ_00406 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
AEOOMBIJ_00407 | 1.4e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AEOOMBIJ_00408 | 9.7e-247 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AEOOMBIJ_00409 | 6.9e-218 | mepA | V | MATE efflux family protein | ||
AEOOMBIJ_00410 | 1.8e-176 | S | SLAP domain | |||
AEOOMBIJ_00411 | 4.4e-283 | M | Peptidase family M1 domain | |||
AEOOMBIJ_00412 | 4.5e-188 | S | Bacteriocin helveticin-J | |||
AEOOMBIJ_00413 | 8e-51 | L | RelB antitoxin | |||
AEOOMBIJ_00414 | 7.4e-105 | qmcA | O | prohibitin homologues | ||
AEOOMBIJ_00415 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
AEOOMBIJ_00416 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AEOOMBIJ_00417 | 4.2e-155 | 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 | |
AEOOMBIJ_00418 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
AEOOMBIJ_00419 | 3.5e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
AEOOMBIJ_00420 | 5.1e-251 | dnaB | L | Replication initiation and membrane attachment | ||
AEOOMBIJ_00421 | 2.1e-168 | dnaI | L | Primosomal protein DnaI | ||
AEOOMBIJ_00422 | 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) | |
AEOOMBIJ_00423 | 2.8e-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 | |
AEOOMBIJ_00424 | 4.8e-34 | S | reductase | |||
AEOOMBIJ_00425 | 4.4e-39 | S | reductase | |||
AEOOMBIJ_00426 | 2.7e-32 | S | reductase | |||
AEOOMBIJ_00427 | 6.4e-148 | yxeH | S | hydrolase | ||
AEOOMBIJ_00428 | 6.2e-249 | yjjP | S | Putative threonine/serine exporter | ||
AEOOMBIJ_00429 | 2.6e-177 | citR | K | Putative sugar-binding domain | ||
AEOOMBIJ_00430 | 1.5e-50 | |||||
AEOOMBIJ_00431 | 5.5e-09 | |||||
AEOOMBIJ_00432 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
AEOOMBIJ_00433 | 1.5e-95 | S | UPF0397 protein | |||
AEOOMBIJ_00434 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00435 | 3.6e-146 | cbiQ | P | cobalt transport | ||
AEOOMBIJ_00436 | 3.5e-21 | |||||
AEOOMBIJ_00437 | 9.3e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
AEOOMBIJ_00438 | 2.1e-288 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AEOOMBIJ_00439 | 2.4e-167 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
AEOOMBIJ_00440 | 1.2e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
AEOOMBIJ_00441 | 6.9e-195 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
AEOOMBIJ_00442 | 1.1e-152 | ydjP | I | Alpha/beta hydrolase family | ||
AEOOMBIJ_00443 | 9.7e-65 | yagE | E | amino acid | ||
AEOOMBIJ_00444 | 8.4e-128 | yagE | E | Amino acid permease | ||
AEOOMBIJ_00445 | 4.3e-86 | 3.4.21.96 | S | SLAP domain | ||
AEOOMBIJ_00446 | 4.6e-160 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AEOOMBIJ_00447 | 1.1e-225 | 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 | |
AEOOMBIJ_00448 | 1.2e-107 | hlyIII | S | protein, hemolysin III | ||
AEOOMBIJ_00449 | 2e-144 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
AEOOMBIJ_00450 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
AEOOMBIJ_00451 | 1.1e-66 | yjcE | P | NhaP-type Na H and K H | ||
AEOOMBIJ_00452 | 1.5e-40 | yjcE | P | Sodium proton antiporter | ||
AEOOMBIJ_00453 | 1.9e-94 | yjcE | P | Sodium proton antiporter | ||
AEOOMBIJ_00454 | 2.8e-154 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
AEOOMBIJ_00455 | 4.6e-132 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AEOOMBIJ_00456 | 5.8e-152 | dprA | LU | DNA protecting protein DprA | ||
AEOOMBIJ_00457 | 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 | |
AEOOMBIJ_00458 | 1.4e-248 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
AEOOMBIJ_00459 | 5e-141 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
AEOOMBIJ_00460 | 1.9e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
AEOOMBIJ_00461 | 8.2e-236 | 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 | ||
AEOOMBIJ_00462 | 4.8e-181 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
AEOOMBIJ_00463 | 1.4e-86 | C | Aldo keto reductase | |||
AEOOMBIJ_00464 | 3.8e-48 | M | LysM domain protein | |||
AEOOMBIJ_00465 | 2.9e-15 | M | LysM domain protein | |||
AEOOMBIJ_00466 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
AEOOMBIJ_00467 | 2.6e-310 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AEOOMBIJ_00468 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
AEOOMBIJ_00469 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AEOOMBIJ_00470 | 3.3e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
AEOOMBIJ_00471 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
AEOOMBIJ_00472 | 1e-167 | cvfB | S | S1 domain | ||
AEOOMBIJ_00473 | 2.9e-165 | xerD | D | recombinase XerD | ||
AEOOMBIJ_00474 | 8.1e-54 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AEOOMBIJ_00475 | 7.6e-132 | 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 | ||
AEOOMBIJ_00476 | 4.1e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
AEOOMBIJ_00477 | 9e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AEOOMBIJ_00478 | 8.7e-114 | 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 | |||
AEOOMBIJ_00479 | 2.7e-18 | M | Lysin motif | |||
AEOOMBIJ_00480 | 2.2e-114 | 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 | |
AEOOMBIJ_00481 | 5.5e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
AEOOMBIJ_00482 | 1.9e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AEOOMBIJ_00483 | 2.3e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
AEOOMBIJ_00484 | 1.4e-75 | S | Tetratricopeptide repeat protein | |||
AEOOMBIJ_00485 | 3.8e-99 | S | Tetratricopeptide repeat protein | |||
AEOOMBIJ_00486 | 1.3e-237 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AEOOMBIJ_00488 | 4.3e-36 | |||||
AEOOMBIJ_00489 | 6.2e-288 | P | ABC transporter | |||
AEOOMBIJ_00490 | 2.3e-07 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AEOOMBIJ_00491 | 9.9e-82 | C | Flavodoxin | |||
AEOOMBIJ_00492 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
AEOOMBIJ_00493 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AEOOMBIJ_00494 | 2.1e-114 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AEOOMBIJ_00495 | 6.8e-181 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AEOOMBIJ_00496 | 1.1e-243 | yfnA | E | Amino Acid | ||
AEOOMBIJ_00497 | 6.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
AEOOMBIJ_00498 | 1e-48 | S | Metal binding domain of Ada | |||
AEOOMBIJ_00499 | 0.0 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
AEOOMBIJ_00500 | 9e-137 | lysR5 | K | LysR substrate binding domain | ||
AEOOMBIJ_00501 | 8.8e-234 | arcA | 3.5.3.6 | E | Arginine | |
AEOOMBIJ_00502 | 4.3e-66 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
AEOOMBIJ_00503 | 2e-105 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
AEOOMBIJ_00504 | 9.2e-95 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
AEOOMBIJ_00505 | 2.3e-215 | S | Sterol carrier protein domain | |||
AEOOMBIJ_00506 | 1e-20 | |||||
AEOOMBIJ_00507 | 4.9e-108 | K | LysR substrate binding domain | |||
AEOOMBIJ_00508 | 9e-98 | |||||
AEOOMBIJ_00509 | 3e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
AEOOMBIJ_00510 | 1.9e-75 | M | LysM domain | |||
AEOOMBIJ_00511 | 1.3e-42 | |||||
AEOOMBIJ_00513 | 4.9e-35 | |||||
AEOOMBIJ_00514 | 4.5e-76 | yniG | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_00515 | 5.4e-237 | L | transposase, IS605 OrfB family | |||
AEOOMBIJ_00516 | 1.4e-109 | yniG | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_00517 | 2.4e-128 | S | cog cog1373 | |||
AEOOMBIJ_00518 | 8.4e-56 | S | Domain of unknown function (DUF4767) | |||
AEOOMBIJ_00519 | 5.8e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
AEOOMBIJ_00520 | 2.5e-147 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
AEOOMBIJ_00521 | 3.2e-101 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AEOOMBIJ_00522 | 5.3e-26 | |||||
AEOOMBIJ_00523 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
AEOOMBIJ_00524 | 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) | |
AEOOMBIJ_00525 | 3.9e-66 | 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 | |
AEOOMBIJ_00526 | 8.5e-139 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
AEOOMBIJ_00527 | 3.3e-132 | coiA | 3.6.4.12 | S | Competence protein | |
AEOOMBIJ_00528 | 4e-13 | coiA | 3.6.4.12 | S | Competence protein | |
AEOOMBIJ_00529 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
AEOOMBIJ_00530 | 6.8e-110 | yjbK | S | CYTH | ||
AEOOMBIJ_00531 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
AEOOMBIJ_00532 | 3.8e-153 | 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 | |
AEOOMBIJ_00533 | 6.4e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AEOOMBIJ_00534 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
AEOOMBIJ_00535 | 4.2e-92 | S | SNARE associated Golgi protein | |||
AEOOMBIJ_00536 | 2.6e-138 | S | TerB-C domain | |||
AEOOMBIJ_00537 | 1.4e-245 | P | P-loop Domain of unknown function (DUF2791) | |||
AEOOMBIJ_00538 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
AEOOMBIJ_00539 | 1.4e-60 | |||||
AEOOMBIJ_00540 | 4.3e-228 | amtB | P | ammonium transporter | ||
AEOOMBIJ_00541 | 4.4e-135 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
AEOOMBIJ_00543 | 6.2e-59 | psiE | S | Phosphate-starvation-inducible E | ||
AEOOMBIJ_00544 | 6.5e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
AEOOMBIJ_00545 | 2.9e-69 | S | Iron-sulphur cluster biosynthesis | |||
AEOOMBIJ_00547 | 2.3e-30 | |||||
AEOOMBIJ_00548 | 2.3e-172 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
AEOOMBIJ_00549 | 6.2e-12 | |||||
AEOOMBIJ_00550 | 1.5e-16 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AEOOMBIJ_00551 | 4.1e-78 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AEOOMBIJ_00552 | 2.8e-86 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AEOOMBIJ_00553 | 5.8e-78 | M | LysM domain protein | |||
AEOOMBIJ_00554 | 9.2e-89 | ypmB | S | Protein conserved in bacteria | ||
AEOOMBIJ_00555 | 1.5e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AEOOMBIJ_00556 | 1.3e-114 | dnaD | L | DnaD domain protein | ||
AEOOMBIJ_00557 | 6.1e-114 | 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 | |
AEOOMBIJ_00558 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AEOOMBIJ_00559 | 4.5e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
AEOOMBIJ_00560 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
AEOOMBIJ_00561 | 1.1e-68 | 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 | ||
AEOOMBIJ_00562 | 3.6e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
AEOOMBIJ_00563 | 1e-242 | cpdA | S | Calcineurin-like phosphoesterase | ||
AEOOMBIJ_00564 | 3.4e-79 | |||||
AEOOMBIJ_00565 | 1.9e-115 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
AEOOMBIJ_00566 | 9.3e-86 | |||||
AEOOMBIJ_00567 | 2.5e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AEOOMBIJ_00568 | 7.7e-182 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
AEOOMBIJ_00569 | 3e-147 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AEOOMBIJ_00570 | 4.4e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
AEOOMBIJ_00571 | 3.7e-156 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
AEOOMBIJ_00572 | 7.3e-126 | S | Alpha/beta hydrolase family | |||
AEOOMBIJ_00573 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
AEOOMBIJ_00574 | 2e-157 | S | reductase | |||
AEOOMBIJ_00575 | 9.3e-35 | |||||
AEOOMBIJ_00576 | 4.4e-103 | K | Putative DNA-binding domain | |||
AEOOMBIJ_00577 | 3.1e-150 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
AEOOMBIJ_00578 | 3e-66 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AEOOMBIJ_00579 | 1e-63 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AEOOMBIJ_00580 | 5e-13 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AEOOMBIJ_00581 | 1.4e-115 | mmuP | E | amino acid | ||
AEOOMBIJ_00582 | 1.4e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AEOOMBIJ_00583 | 6.3e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
AEOOMBIJ_00584 | 1.7e-284 | E | Amino acid permease | |||
AEOOMBIJ_00585 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
AEOOMBIJ_00586 | 2.3e-245 | ynbB | 4.4.1.1 | P | aluminum resistance | |
AEOOMBIJ_00587 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AEOOMBIJ_00588 | 2e-106 | S | domain protein | |||
AEOOMBIJ_00589 | 2.5e-140 | V | ABC transporter | |||
AEOOMBIJ_00590 | 5.9e-68 | S | Protein of unknown function (DUF3021) | |||
AEOOMBIJ_00591 | 6e-86 | |||||
AEOOMBIJ_00592 | 4.4e-172 | S | Domain of unknown function (DUF389) | |||
AEOOMBIJ_00593 | 7.4e-40 | yabO | J | S4 domain protein | ||
AEOOMBIJ_00594 | 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 | ||
AEOOMBIJ_00595 | 5.1e-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 | |
AEOOMBIJ_00596 | 1.5e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AEOOMBIJ_00597 | 3.4e-129 | S | (CBS) domain | |||
AEOOMBIJ_00598 | 4.7e-182 | pepA | E | M42 glutamyl aminopeptidase | ||
AEOOMBIJ_00599 | 2.2e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00600 | 5.9e-174 | S | Aldo keto reductase | |||
AEOOMBIJ_00601 | 2.7e-138 | |||||
AEOOMBIJ_00602 | 2.8e-202 | steT | E | amino acid | ||
AEOOMBIJ_00603 | 2.4e-26 | steT | E | amino acid | ||
AEOOMBIJ_00604 | 8.6e-243 | steT | E | amino acid | ||
AEOOMBIJ_00605 | 1.9e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
AEOOMBIJ_00606 | 1.9e-147 | glnH | ET | ABC transporter | ||
AEOOMBIJ_00607 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
AEOOMBIJ_00608 | 6.9e-309 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00609 | 0.0 | V | ABC transporter transmembrane region | |||
AEOOMBIJ_00610 | 1.6e-100 | S | ABC-type cobalt transport system, permease component | |||
AEOOMBIJ_00611 | 1e-246 | G | MFS/sugar transport protein | |||
AEOOMBIJ_00612 | 9.8e-39 | udk | 2.7.1.48 | F | Zeta toxin | |
AEOOMBIJ_00613 | 3.8e-46 | udk | 2.7.1.48 | F | Zeta toxin | |
AEOOMBIJ_00614 | 4.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AEOOMBIJ_00615 | 1.2e-146 | glnH | ET | ABC transporter substrate-binding protein | ||
AEOOMBIJ_00616 | 3.7e-90 | gluC | P | ABC transporter permease | ||
AEOOMBIJ_00617 | 4.7e-109 | glnP | P | ABC transporter permease | ||
AEOOMBIJ_00618 | 1.1e-164 | S | Protein of unknown function (DUF2974) | |||
AEOOMBIJ_00619 | 5.6e-86 | |||||
AEOOMBIJ_00620 | 6.3e-212 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AEOOMBIJ_00621 | 1.3e-235 | G | Bacterial extracellular solute-binding protein | |||
AEOOMBIJ_00622 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
AEOOMBIJ_00623 | 1e-165 | 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 | |
AEOOMBIJ_00624 | 1e-125 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
AEOOMBIJ_00625 | 0.0 | kup | P | Transport of potassium into the cell | ||
AEOOMBIJ_00626 | 9.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
AEOOMBIJ_00627 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
AEOOMBIJ_00628 | 1.2e-154 | S | hydrolase | |||
AEOOMBIJ_00629 | 2.5e-59 | S | Enterocin A Immunity | |||
AEOOMBIJ_00630 | 3.1e-136 | glcR | K | DeoR C terminal sensor domain | ||
AEOOMBIJ_00631 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AEOOMBIJ_00632 | 2e-160 | rssA | S | Phospholipase, patatin family | ||
AEOOMBIJ_00633 | 5.4e-147 | S | hydrolase | |||
AEOOMBIJ_00634 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
AEOOMBIJ_00635 | 4.1e-147 | glvR | K | Helix-turn-helix domain, rpiR family | ||
AEOOMBIJ_00636 | 1.6e-80 | |||||
AEOOMBIJ_00637 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
AEOOMBIJ_00638 | 2.1e-39 | |||||
AEOOMBIJ_00639 | 3.9e-119 | C | nitroreductase | |||
AEOOMBIJ_00640 | 1.7e-249 | yhdP | S | Transporter associated domain | ||
AEOOMBIJ_00641 | 3.4e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AEOOMBIJ_00642 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
AEOOMBIJ_00643 | 9.6e-103 | pgm3 | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
AEOOMBIJ_00644 | 8.8e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AEOOMBIJ_00645 | 2.6e-280 | thrC | 4.2.3.1 | E | Threonine synthase | |
AEOOMBIJ_00646 | 6.6e-221 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AEOOMBIJ_00647 | 2.8e-157 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
AEOOMBIJ_00648 | 9.4e-118 | |||||
AEOOMBIJ_00649 | 4.6e-160 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AEOOMBIJ_00651 | 1.8e-104 | 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 | |
AEOOMBIJ_00652 | 1.3e-116 | S | Peptidase family M23 | |||
AEOOMBIJ_00653 | 1.2e-188 | K | Periplasmic binding protein-like domain | |||
AEOOMBIJ_00654 | 2e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
AEOOMBIJ_00655 | 7.6e-163 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
AEOOMBIJ_00656 | 5.3e-189 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
AEOOMBIJ_00657 | 2.1e-142 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
AEOOMBIJ_00658 | 9.3e-80 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AEOOMBIJ_00659 | 7.2e-221 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
AEOOMBIJ_00660 | 5.4e-165 | lacR | K | Transcriptional regulator | ||
AEOOMBIJ_00661 | 8.9e-207 | lacS | G | Transporter | ||
AEOOMBIJ_00662 | 5.7e-103 | lacS | G | Transporter | ||
AEOOMBIJ_00663 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
AEOOMBIJ_00664 | 1.1e-220 | 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) | |
AEOOMBIJ_00665 | 2e-288 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AEOOMBIJ_00666 | 1.2e-196 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AEOOMBIJ_00667 | 3.1e-71 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
AEOOMBIJ_00668 | 7.7e-26 | |||||
AEOOMBIJ_00669 | 5.7e-84 | S | PFAM Archaeal ATPase | |||
AEOOMBIJ_00670 | 2.2e-85 | S | PFAM Archaeal ATPase | |||
AEOOMBIJ_00671 | 5.5e-36 | |||||
AEOOMBIJ_00672 | 1.7e-160 | scrR | K | Periplasmic binding protein domain | ||
AEOOMBIJ_00673 | 1.5e-141 | msmE | G | Bacterial extracellular solute-binding protein | ||
AEOOMBIJ_00674 | 7e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
AEOOMBIJ_00675 | 4.1e-80 | fld | C | Flavodoxin | ||
AEOOMBIJ_00676 | 1.4e-163 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
AEOOMBIJ_00677 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
AEOOMBIJ_00678 | 2.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
AEOOMBIJ_00679 | 2.5e-214 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
AEOOMBIJ_00680 | 3.6e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
AEOOMBIJ_00681 | 6e-46 | L | An automated process has identified a potential problem with this gene model | |||
AEOOMBIJ_00682 | 2.8e-48 | S | Peptidase propeptide and YPEB domain | |||
AEOOMBIJ_00683 | 4.1e-33 | adh | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
AEOOMBIJ_00684 | 3.3e-237 | L | COG2963 Transposase and inactivated derivatives | |||
AEOOMBIJ_00685 | 4.7e-46 | pspC | KT | PspC domain | ||
AEOOMBIJ_00687 | 1.3e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AEOOMBIJ_00688 | 2.8e-154 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
AEOOMBIJ_00689 | 6.7e-98 | M | ErfK YbiS YcfS YnhG | |||
AEOOMBIJ_00690 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
AEOOMBIJ_00691 | 4.6e-171 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
AEOOMBIJ_00692 | 9e-20 | ywzB | S | Protein of unknown function (DUF1146) | ||
AEOOMBIJ_00693 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AEOOMBIJ_00694 | 3.3e-240 | 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 | |
AEOOMBIJ_00695 | 2e-172 | 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 | ||
AEOOMBIJ_00696 | 2.8e-282 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
AEOOMBIJ_00697 | 2.8e-91 | 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 | ||
AEOOMBIJ_00698 | 3.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
AEOOMBIJ_00699 | 3.5e-27 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
AEOOMBIJ_00700 | 3.8e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
AEOOMBIJ_00701 | 6.8e-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 | |
AEOOMBIJ_00702 | 3.7e-190 | 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 | |
AEOOMBIJ_00703 | 7.3e-155 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
AEOOMBIJ_00704 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AEOOMBIJ_00705 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
AEOOMBIJ_00706 | 1.7e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AEOOMBIJ_00709 | 3.9e-195 | ampC | V | Beta-lactamase | ||
AEOOMBIJ_00710 | 3.8e-217 | EGP | Major facilitator Superfamily | |||
AEOOMBIJ_00711 | 3.2e-253 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
AEOOMBIJ_00712 | 3.8e-105 | vanZ | V | VanZ like family | ||
AEOOMBIJ_00713 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AEOOMBIJ_00714 | 7.2e-267 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
AEOOMBIJ_00715 | 1e-47 | K | Transcriptional regulatory protein, C terminal | |||
AEOOMBIJ_00716 | 2.6e-60 | K | Transcriptional regulatory protein, C terminal | |||
AEOOMBIJ_00717 | 7.7e-67 | S | SdpI/YhfL protein family | |||
AEOOMBIJ_00718 | 1.6e-190 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
AEOOMBIJ_00719 | 9.9e-227 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
AEOOMBIJ_00720 | 2.5e-89 | M | Protein of unknown function (DUF3737) | |||
AEOOMBIJ_00722 | 6.3e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AEOOMBIJ_00723 | 1.9e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
AEOOMBIJ_00724 | 1.6e-21 | |||||
AEOOMBIJ_00725 | 3.8e-77 | comGF | U | Putative Competence protein ComGF | ||
AEOOMBIJ_00726 | 2.3e-41 | |||||
AEOOMBIJ_00727 | 1.8e-69 | |||||
AEOOMBIJ_00728 | 3.1e-43 | comGC | U | competence protein ComGC | ||
AEOOMBIJ_00729 | 1.7e-171 | comGB | NU | type II secretion system | ||
AEOOMBIJ_00730 | 1.7e-179 | comGA | NU | Type II IV secretion system protein | ||
AEOOMBIJ_00731 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
AEOOMBIJ_00732 | 7.6e-94 | S | VanZ like family | |||
AEOOMBIJ_00733 | 3.5e-101 | ylbE | GM | NAD(P)H-binding | ||
AEOOMBIJ_00734 | 3.7e-27 | 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 | ||
AEOOMBIJ_00736 | 1.3e-160 | L | hmm pf00665 | |||
AEOOMBIJ_00737 | 5.8e-100 | L | Helix-turn-helix domain | |||
AEOOMBIJ_00738 | 2e-310 | E | Amino acid permease | |||
AEOOMBIJ_00740 | 8.8e-82 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
AEOOMBIJ_00741 | 2.2e-90 | 2.7.7.65 | T | GGDEF domain | ||
AEOOMBIJ_00742 | 8.2e-36 | |||||
AEOOMBIJ_00743 | 5.2e-112 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
AEOOMBIJ_00744 | 3.7e-26 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
AEOOMBIJ_00745 | 1.2e-92 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
AEOOMBIJ_00746 | 1e-149 | D | Alpha beta | |||
AEOOMBIJ_00747 | 1e-297 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
AEOOMBIJ_00748 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
AEOOMBIJ_00749 | 7e-142 | licT | K | CAT RNA binding domain | ||
AEOOMBIJ_00750 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AEOOMBIJ_00751 | 7.4e-85 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
AEOOMBIJ_00752 | 1.6e-118 | |||||
AEOOMBIJ_00753 | 1.8e-75 | K | Penicillinase repressor | |||
AEOOMBIJ_00754 | 1.4e-147 | S | hydrolase | |||
AEOOMBIJ_00755 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
AEOOMBIJ_00756 | 2e-172 | ybbR | S | YbbR-like protein | ||
AEOOMBIJ_00757 | 6.4e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
AEOOMBIJ_00758 | 7.3e-208 | potD | P | ABC transporter | ||
AEOOMBIJ_00759 | 4.8e-127 | potC | P | ABC transporter permease | ||
AEOOMBIJ_00760 | 1.3e-129 | potB | P | ABC transporter permease | ||
AEOOMBIJ_00761 | 1.8e-206 | 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 | |
AEOOMBIJ_00762 | 2e-163 | murB | 1.3.1.98 | M | Cell wall formation | |
AEOOMBIJ_00763 | 4e-98 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
AEOOMBIJ_00764 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
AEOOMBIJ_00765 | 4.1e-181 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
AEOOMBIJ_00766 | 9.7e-137 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
AEOOMBIJ_00767 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
AEOOMBIJ_00768 | 1.2e-94 | |||||
AEOOMBIJ_00769 | 6e-199 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
AEOOMBIJ_00770 | 1.7e-142 | 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) | |
AEOOMBIJ_00771 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
AEOOMBIJ_00772 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
AEOOMBIJ_00773 | 2.6e-189 | cggR | K | Putative sugar-binding domain | ||
AEOOMBIJ_00775 | 2.8e-290 | |||||
AEOOMBIJ_00776 | 4.6e-274 | ycaM | E | amino acid | ||
AEOOMBIJ_00777 | 3.1e-139 | S | Cysteine-rich secretory protein family | |||
AEOOMBIJ_00778 | 4.2e-77 | K | MerR HTH family regulatory protein | |||
AEOOMBIJ_00779 | 2.4e-262 | lmrB | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_00780 | 3.1e-48 | S | Domain of unknown function (DUF4811) | |||
AEOOMBIJ_00781 | 4.3e-48 | U | TraM recognition site of TraD and TraG | |||
AEOOMBIJ_00785 | 1e-30 | M | domain protein | |||
AEOOMBIJ_00786 | 7.2e-15 | S | SLAP domain | |||
AEOOMBIJ_00787 | 7.4e-40 | M | domain protein | |||
AEOOMBIJ_00789 | 1.4e-24 | srtA | 3.4.22.70 | M | sortase family | |
AEOOMBIJ_00790 | 2.3e-21 | S | SLAP domain | |||
AEOOMBIJ_00795 | 5.7e-11 | S | Single-strand binding protein family | |||
AEOOMBIJ_00806 | 1.7e-25 | S | Domain of unknown function (DUF771) | |||
AEOOMBIJ_00807 | 2e-32 | K | Helix-turn-helix domain | |||
AEOOMBIJ_00808 | 5.7e-16 | K | Helix-turn-helix XRE-family like proteins | |||
AEOOMBIJ_00809 | 3.4e-29 | K | Helix-turn-helix XRE-family like proteins | |||
AEOOMBIJ_00810 | 5e-08 | S | Pfam:DUF955 | |||
AEOOMBIJ_00811 | 6.4e-111 | L | Belongs to the 'phage' integrase family | |||
AEOOMBIJ_00813 | 1.6e-131 | I | Carboxylesterase family | |||
AEOOMBIJ_00814 | 5.6e-183 | K | Transcriptional regulator | |||
AEOOMBIJ_00815 | 2.1e-171 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AEOOMBIJ_00816 | 2.7e-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 | |
AEOOMBIJ_00817 | 4e-57 | K | Helix-turn-helix domain | |||
AEOOMBIJ_00818 | 7.5e-118 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AEOOMBIJ_00819 | 2.3e-139 | 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 | |
AEOOMBIJ_00820 | 5e-145 | 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 | |
AEOOMBIJ_00821 | 1.2e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
AEOOMBIJ_00822 | 3.9e-163 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AEOOMBIJ_00823 | 2.8e-157 | pstS | P | Phosphate | ||
AEOOMBIJ_00824 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
AEOOMBIJ_00825 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
AEOOMBIJ_00826 | 1.2e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
AEOOMBIJ_00827 | 3.6e-24 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
AEOOMBIJ_00828 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
AEOOMBIJ_00829 | 5.8e-288 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
AEOOMBIJ_00830 | 1.7e-34 | |||||
AEOOMBIJ_00831 | 5.5e-95 | sigH | K | Belongs to the sigma-70 factor family | ||
AEOOMBIJ_00832 | 1.7e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AEOOMBIJ_00833 | 2.3e-75 | 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) | ||
AEOOMBIJ_00834 | 2.9e-276 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AEOOMBIJ_00835 | 1.9e-291 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
AEOOMBIJ_00836 | 2.7e-255 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
AEOOMBIJ_00837 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
AEOOMBIJ_00838 | 1.9e-52 | |||||
AEOOMBIJ_00839 | 3.9e-267 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AEOOMBIJ_00840 | 1.1e-183 | S | AAA domain | |||
AEOOMBIJ_00841 | 1.2e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
AEOOMBIJ_00842 | 1.4e-23 | |||||
AEOOMBIJ_00843 | 7.3e-161 | czcD | P | cation diffusion facilitator family transporter | ||
AEOOMBIJ_00844 | 3.7e-125 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
AEOOMBIJ_00845 | 6e-132 | S | membrane transporter protein | |||
AEOOMBIJ_00846 | 1.9e-118 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
AEOOMBIJ_00847 | 6.3e-105 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
AEOOMBIJ_00848 | 1.2e-49 | S | Protein of unknown function (DUF3021) | |||
AEOOMBIJ_00849 | 2.8e-65 | K | LytTr DNA-binding domain | |||
AEOOMBIJ_00850 | 1.2e-10 | |||||
AEOOMBIJ_00851 | 1.3e-55 | K | Acetyltransferase (GNAT) domain | |||
AEOOMBIJ_00852 | 1.9e-12 | L | Transposase | |||
AEOOMBIJ_00853 | 1.4e-16 | L | Transposase | |||
AEOOMBIJ_00854 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
AEOOMBIJ_00855 | 5.7e-272 | P | Sodium:sulfate symporter transmembrane region | |||
AEOOMBIJ_00856 | 1.3e-133 | hxlA | 6.2.1.3 | H | Aldolase/RraA | |
AEOOMBIJ_00857 | 3.5e-252 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AEOOMBIJ_00858 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AEOOMBIJ_00859 | 1.9e-261 | frdC | 1.3.5.4 | C | FAD binding domain | |
AEOOMBIJ_00860 | 9e-267 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
AEOOMBIJ_00861 | 3.4e-73 | metI | P | ABC transporter permease | ||
AEOOMBIJ_00862 | 2.6e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AEOOMBIJ_00863 | 5.9e-160 | metQ2 | P | Belongs to the nlpA lipoprotein family | ||
AEOOMBIJ_00864 | 2.4e-175 | F | DNA/RNA non-specific endonuclease | |||
AEOOMBIJ_00865 | 0.0 | aha1 | P | E1-E2 ATPase | ||
AEOOMBIJ_00866 | 1.5e-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 | |
AEOOMBIJ_00867 | 1.3e-179 | 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 | |
AEOOMBIJ_00868 | 1.2e-250 | yifK | E | Amino acid permease | ||
AEOOMBIJ_00869 | 3.7e-263 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AEOOMBIJ_00870 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
AEOOMBIJ_00871 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
AEOOMBIJ_00872 | 9.4e-305 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
AEOOMBIJ_00873 | 1.4e-140 | hlyX | S | Transporter associated domain | ||
AEOOMBIJ_00874 | 2.7e-74 | |||||
AEOOMBIJ_00875 | 1.6e-85 | |||||
AEOOMBIJ_00876 | 1.5e-144 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
AEOOMBIJ_00877 | 4.6e-263 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AEOOMBIJ_00878 | 1.4e-118 | D | Alpha beta | |||
AEOOMBIJ_00879 | 6.1e-269 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
AEOOMBIJ_00880 | 1.2e-127 | K | LytTr DNA-binding domain | |||
AEOOMBIJ_00881 | 4.4e-138 | 2.7.13.3 | T | GHKL domain | ||
AEOOMBIJ_00882 | 1.2e-16 | |||||
AEOOMBIJ_00883 | 1.3e-159 | degV | S | EDD domain protein, DegV family | ||
AEOOMBIJ_00884 | 1.1e-66 | |||||
AEOOMBIJ_00885 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
AEOOMBIJ_00886 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AEOOMBIJ_00887 | 1e-198 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AEOOMBIJ_00888 | 4.3e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AEOOMBIJ_00889 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
AEOOMBIJ_00890 | 1.8e-285 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
AEOOMBIJ_00891 | 5.5e-53 | |||||
AEOOMBIJ_00893 | 2.7e-34 | S | YSIRK type signal peptide | |||
AEOOMBIJ_00894 | 1.9e-110 | F | DNA/RNA non-specific endonuclease | |||
AEOOMBIJ_00895 | 2e-75 | S | cog cog0433 | |||
AEOOMBIJ_00896 | 2.7e-83 | S | Protein of unknown function (DUF1211) | |||
AEOOMBIJ_00897 | 3.1e-113 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
AEOOMBIJ_00898 | 2.8e-119 | 3.6.1.55 | F | NUDIX domain | ||
AEOOMBIJ_00899 | 3e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AEOOMBIJ_00900 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
AEOOMBIJ_00901 | 2.5e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
AEOOMBIJ_00929 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
AEOOMBIJ_00930 | 7.6e-202 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
AEOOMBIJ_00931 | 1.4e-176 | 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 | ||
AEOOMBIJ_00932 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
AEOOMBIJ_00933 | 1.7e-29 | secG | U | Preprotein translocase | ||
AEOOMBIJ_00934 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AEOOMBIJ_00935 | 5.1e-78 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
AEOOMBIJ_00936 | 1.3e-229 | S | Putative peptidoglycan binding domain | |||
AEOOMBIJ_00937 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
AEOOMBIJ_00938 | 2.8e-98 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
AEOOMBIJ_00939 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
AEOOMBIJ_00940 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
AEOOMBIJ_00941 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
AEOOMBIJ_00942 | 7.4e-205 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
AEOOMBIJ_00943 | 2.1e-78 | 2.7.13.3 | T | GHKL domain | ||
AEOOMBIJ_00944 | 2.9e-79 | K | LytTr DNA-binding domain | |||
AEOOMBIJ_00945 | 8.7e-30 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
AEOOMBIJ_00946 | 7.8e-52 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AEOOMBIJ_00947 | 2.6e-275 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AEOOMBIJ_00948 | 3.4e-27 | |||||
AEOOMBIJ_00949 | 8e-22 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
AEOOMBIJ_00950 | 5.4e-53 | hipB | K | sequence-specific DNA binding | ||
AEOOMBIJ_00951 | 4.8e-42 | S | SnoaL-like domain | |||
AEOOMBIJ_00952 | 0.0 | L | PLD-like domain | |||
AEOOMBIJ_00954 | 2.9e-23 | |||||
AEOOMBIJ_00955 | 1.9e-186 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AEOOMBIJ_00956 | 0.0 | L | AAA domain | |||
AEOOMBIJ_00957 | 1e-226 | yhaO | L | Ser Thr phosphatase family protein | ||
AEOOMBIJ_00958 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
AEOOMBIJ_00959 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
AEOOMBIJ_00960 | 4.2e-150 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AEOOMBIJ_00961 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AEOOMBIJ_00962 | 4.2e-101 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
AEOOMBIJ_00963 | 2.5e-86 | K | GNAT family | |||
AEOOMBIJ_00964 | 2.7e-202 | XK27_00915 | C | Luciferase-like monooxygenase | ||
AEOOMBIJ_00965 | 4.7e-36 | rbtT | P | Major Facilitator Superfamily | ||
AEOOMBIJ_00966 | 3.9e-33 | I | Carboxylesterase family | |||
AEOOMBIJ_00967 | 1.5e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
AEOOMBIJ_00968 | 2.9e-277 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AEOOMBIJ_00969 | 4.5e-291 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AEOOMBIJ_00970 | 1.7e-148 | S | haloacid dehalogenase-like hydrolase | |||
AEOOMBIJ_00971 | 7e-50 | |||||
AEOOMBIJ_00972 | 1.9e-37 | |||||
AEOOMBIJ_00973 | 1.2e-63 | S | Alpha beta hydrolase | |||
AEOOMBIJ_00974 | 1e-23 | S | Alpha beta hydrolase | |||
AEOOMBIJ_00975 | 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 | |
AEOOMBIJ_00976 | 6.4e-243 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
AEOOMBIJ_00977 | 8.2e-177 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
AEOOMBIJ_00978 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
AEOOMBIJ_00979 | 1.9e-269 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
AEOOMBIJ_00980 | 2.2e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
AEOOMBIJ_00981 | 9.7e-175 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AEOOMBIJ_00982 | 1.1e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
AEOOMBIJ_00983 | 2.4e-231 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
AEOOMBIJ_00984 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
AEOOMBIJ_00985 | 2.3e-84 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
AEOOMBIJ_00986 | 2.8e-168 | K | LysR substrate binding domain | |||
AEOOMBIJ_00987 | 1.1e-121 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AEOOMBIJ_00988 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
AEOOMBIJ_00989 | 4.7e-275 | ytgP | S | Polysaccharide biosynthesis protein | ||
AEOOMBIJ_00990 | 1.4e-191 | oppA | E | ABC transporter, substratebinding protein | ||
AEOOMBIJ_00991 | 1.3e-30 | |||||
AEOOMBIJ_00992 | 1.2e-144 | pstS | P | Phosphate | ||
AEOOMBIJ_00993 | 2.1e-160 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
AEOOMBIJ_00994 | 1.2e-152 | pstA | P | Phosphate transport system permease protein PstA | ||
AEOOMBIJ_00995 | 3.9e-139 | 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 | |
AEOOMBIJ_00996 | 1.4e-105 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
AEOOMBIJ_00997 | 9.5e-121 | T | Transcriptional regulatory protein, C terminal | |||
AEOOMBIJ_00998 | 1.1e-282 | phoR | 2.7.13.3 | T | Histidine kinase | |
AEOOMBIJ_00999 | 1.9e-138 | 2.4.2.3 | F | Phosphorylase superfamily | ||
AEOOMBIJ_01000 | 9e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
AEOOMBIJ_01001 | 3.6e-151 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
AEOOMBIJ_01002 | 1.1e-183 | scrR | K | helix_turn _helix lactose operon repressor | ||
AEOOMBIJ_01003 | 3.7e-295 | scrB | 3.2.1.26 | GH32 | G | invertase |
AEOOMBIJ_01004 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
AEOOMBIJ_01005 | 2.3e-181 | M | CHAP domain | |||
AEOOMBIJ_01006 | 3.5e-75 | |||||
AEOOMBIJ_01007 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
AEOOMBIJ_01008 | 5.9e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
AEOOMBIJ_01009 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
AEOOMBIJ_01010 | 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 | ||
AEOOMBIJ_01011 | 1.7e-102 | 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 | |
AEOOMBIJ_01012 | 1.5e-186 | 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 | |
AEOOMBIJ_01013 | 9.6e-41 | yajC | U | Preprotein translocase | ||
AEOOMBIJ_01014 | 9.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
AEOOMBIJ_01015 | 6.2e-210 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
AEOOMBIJ_01016 | 1.4e-181 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
AEOOMBIJ_01017 | 2e-226 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
AEOOMBIJ_01018 | 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 | |
AEOOMBIJ_01019 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
AEOOMBIJ_01020 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
AEOOMBIJ_01021 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
AEOOMBIJ_01022 | 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 | ||
AEOOMBIJ_01023 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
AEOOMBIJ_01024 | 9.7e-59 | 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 | ||
AEOOMBIJ_01025 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
AEOOMBIJ_01026 | 6.6e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
AEOOMBIJ_01027 | 1.1e-110 | 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 | |
AEOOMBIJ_01028 | 7.7e-30 | ropB | K | Helix-turn-helix domain | ||
AEOOMBIJ_01029 | 2.2e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AEOOMBIJ_01030 | 1.9e-191 | yrvN | L | AAA C-terminal domain | ||
AEOOMBIJ_01031 | 8.2e-64 | spxA_2 | 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 | |
AEOOMBIJ_01032 | 3.3e-283 | treB | G | phosphotransferase system | ||
AEOOMBIJ_01033 | 1.2e-100 | treR | K | UTRA | ||
AEOOMBIJ_01034 | 1e-288 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AEOOMBIJ_01035 | 2e-234 | mepA | V | MATE efflux family protein | ||
AEOOMBIJ_01036 | 3.5e-71 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
AEOOMBIJ_01037 | 1.8e-58 | S | Putative adhesin | |||
AEOOMBIJ_01038 | 5.6e-101 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
AEOOMBIJ_01039 | 3.8e-20 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
AEOOMBIJ_01040 | 1.1e-83 | dps | P | Belongs to the Dps family | ||
AEOOMBIJ_01041 | 2e-178 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
AEOOMBIJ_01043 | 5.6e-191 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AEOOMBIJ_01044 | 1.5e-304 | 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 | ||
AEOOMBIJ_01045 | 5.4e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
AEOOMBIJ_01046 | 4.1e-67 | |||||
AEOOMBIJ_01047 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
AEOOMBIJ_01048 | 5.8e-211 | M | Glycosyl hydrolases family 25 | |||
AEOOMBIJ_01049 | 1.2e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
AEOOMBIJ_01050 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
AEOOMBIJ_01051 | 3.3e-33 | S | Protein of unknown function (DUF2969) | |||
AEOOMBIJ_01052 | 4.7e-216 | rodA | D | Belongs to the SEDS family | ||
AEOOMBIJ_01053 | 1.8e-78 | usp6 | T | universal stress protein | ||
AEOOMBIJ_01054 | 8.4e-39 | |||||
AEOOMBIJ_01055 | 2.2e-238 | rarA | L | recombination factor protein RarA | ||
AEOOMBIJ_01056 | 1.3e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
AEOOMBIJ_01057 | 1.4e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
AEOOMBIJ_01058 | 2.1e-294 | 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 | ||
AEOOMBIJ_01059 | 1.4e-212 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
AEOOMBIJ_01060 | 2e-225 | 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 | |
AEOOMBIJ_01061 | 1.7e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
AEOOMBIJ_01062 | 3.2e-119 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AEOOMBIJ_01063 | 5.5e-44 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
AEOOMBIJ_01064 | 3.5e-62 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
AEOOMBIJ_01065 | 5.2e-170 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
AEOOMBIJ_01066 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
AEOOMBIJ_01067 | 6.5e-44 | |||||
AEOOMBIJ_01069 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
AEOOMBIJ_01070 | 1.1e-132 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
AEOOMBIJ_01071 | 2.5e-52 | |||||
AEOOMBIJ_01072 | 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 | |
AEOOMBIJ_01073 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AEOOMBIJ_01074 | 5.7e-126 | S | Haloacid dehalogenase-like hydrolase | |||
AEOOMBIJ_01075 | 2.3e-108 | radC | L | DNA repair protein | ||
AEOOMBIJ_01076 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
AEOOMBIJ_01077 | 2e-147 | mreC | M | Involved in formation and maintenance of cell shape | ||
AEOOMBIJ_01078 | 2.7e-94 | mreD | ||||
AEOOMBIJ_01080 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
AEOOMBIJ_01081 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
AEOOMBIJ_01082 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AEOOMBIJ_01083 | 1.8e-54 | ftsL | D | Cell division protein FtsL | ||
AEOOMBIJ_01084 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AEOOMBIJ_01085 | 1.5e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
AEOOMBIJ_01086 | 5e-262 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AEOOMBIJ_01087 | 3.7e-207 | 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) |
AEOOMBIJ_01088 | 4.5e-152 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AEOOMBIJ_01089 | 1.3e-246 | 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 | ||
AEOOMBIJ_01090 | 3.8e-206 | 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 | ||
AEOOMBIJ_01091 | 7.3e-74 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
AEOOMBIJ_01092 | 1.7e-45 | yggT | S | YGGT family | ||
AEOOMBIJ_01093 | 5.7e-149 | ylmH | S | S4 domain protein | ||
AEOOMBIJ_01094 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
AEOOMBIJ_01095 | 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) | |
AEOOMBIJ_01096 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
AEOOMBIJ_01097 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
AEOOMBIJ_01098 | 6.7e-37 | |||||
AEOOMBIJ_01099 | 1.2e-126 | 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 | |
AEOOMBIJ_01100 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
AEOOMBIJ_01101 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
AEOOMBIJ_01102 | 5.1e-220 | 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 | |
AEOOMBIJ_01103 | 3.9e-127 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AEOOMBIJ_01104 | 8.3e-106 | S | Repeat protein | |||
AEOOMBIJ_01105 | 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 | |
AEOOMBIJ_01106 | 1.6e-294 | L | Nuclease-related domain | |||
AEOOMBIJ_01107 | 2.3e-164 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
AEOOMBIJ_01108 | 9.3e-147 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AEOOMBIJ_01109 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
AEOOMBIJ_01110 | 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 | |
AEOOMBIJ_01111 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AEOOMBIJ_01112 | 7.6e-49 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
AEOOMBIJ_01113 | 6.8e-243 | cycA | E | Amino acid permease | ||
AEOOMBIJ_01114 | 1.3e-85 | maa | S | transferase hexapeptide repeat | ||
AEOOMBIJ_01115 | 3.3e-158 | K | Transcriptional regulator | |||
AEOOMBIJ_01116 | 1.1e-62 | manO | S | Domain of unknown function (DUF956) | ||
AEOOMBIJ_01117 | 1e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
AEOOMBIJ_01118 | 1.7e-129 | manY | G | PTS system | ||
AEOOMBIJ_01119 | 2.5e-186 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
AEOOMBIJ_01120 | 1.4e-31 | O | OsmC-like protein | |||
AEOOMBIJ_01122 | 1.5e-36 | oppA | E | ABC transporter substrate-binding protein | ||
AEOOMBIJ_01123 | 2.6e-61 | M | Glycosyl hydrolases family 25 | |||
AEOOMBIJ_01124 | 1.3e-61 | M | Glycosyl hydrolases family 25 | |||
AEOOMBIJ_01125 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AEOOMBIJ_01126 | 4.7e-249 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AEOOMBIJ_01128 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
AEOOMBIJ_01129 | 1.3e-30 | |||||
AEOOMBIJ_01130 | 3.6e-69 | T | Toxin-antitoxin system, toxin component, MazF family | |||
AEOOMBIJ_01131 | 3.7e-102 | L | Integrase | |||
AEOOMBIJ_01132 | 2.4e-44 | |||||
AEOOMBIJ_01133 | 1.3e-284 | lsa | S | ABC transporter | ||
AEOOMBIJ_01134 | 8.1e-126 | S | PAS domain | |||
AEOOMBIJ_01135 | 1.6e-11 | |||||
AEOOMBIJ_01136 | 2.7e-57 | |||||
AEOOMBIJ_01137 | 6.6e-56 | |||||
AEOOMBIJ_01138 | 4e-08 | |||||
AEOOMBIJ_01139 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
AEOOMBIJ_01140 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_01141 | 8.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AEOOMBIJ_01142 | 7.6e-239 | pyrP | F | Permease | ||
AEOOMBIJ_01143 | 6e-21 | K | Putative DNA-binding domain | |||
AEOOMBIJ_01144 | 2.5e-63 | rbtT | P | Major Facilitator Superfamily | ||
AEOOMBIJ_01145 | 4.2e-63 | lmrB | EGP | Major facilitator Superfamily | ||
AEOOMBIJ_01146 | 8.5e-87 | 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 | |
AEOOMBIJ_01147 | 6.8e-60 | divIC | D | Septum formation initiator | ||
AEOOMBIJ_01148 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
AEOOMBIJ_01149 | 2.6e-241 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
AEOOMBIJ_01150 | 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 | ||
AEOOMBIJ_01151 | 2.2e-165 | 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 | ||
AEOOMBIJ_01152 | 2e-194 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
AEOOMBIJ_01153 | 1.1e-297 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AEOOMBIJ_01154 | 1.4e-83 | K | FR47-like protein | |||
AEOOMBIJ_01155 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
AEOOMBIJ_01156 | 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 | ||
AEOOMBIJ_01157 | 4.6e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
AEOOMBIJ_01158 | 5.1e-17 | |||||
AEOOMBIJ_01159 | 5.8e-180 | 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 | ||
AEOOMBIJ_01160 | 9.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
AEOOMBIJ_01161 | 1.1e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
AEOOMBIJ_01162 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
AEOOMBIJ_01163 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
AEOOMBIJ_01164 | 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 | ||
AEOOMBIJ_01165 | 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 | ||
AEOOMBIJ_01166 | 4.1e-90 | S | Short repeat of unknown function (DUF308) | |||
AEOOMBIJ_01167 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
AEOOMBIJ_01168 | 4e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
AEOOMBIJ_01169 | 2.1e-171 | whiA | K | May be required for sporulation | ||
AEOOMBIJ_01170 | 2.3e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
AEOOMBIJ_01171 | 0.0 | S | SH3-like domain | |||
AEOOMBIJ_01172 | 1.4e-51 | |||||
AEOOMBIJ_01173 | 2.1e-42 | |||||
AEOOMBIJ_01174 | 6.4e-232 | 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 | |
AEOOMBIJ_01175 | 9.5e-297 | ybeC | E | amino acid | ||
AEOOMBIJ_01176 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AEOOMBIJ_01177 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
AEOOMBIJ_01178 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
AEOOMBIJ_01179 | 8e-260 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
AEOOMBIJ_01180 | 4e-249 | 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 | |
AEOOMBIJ_01181 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
AEOOMBIJ_01182 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
AEOOMBIJ_01183 | 4.7e-26 | K | FCD | |||
AEOOMBIJ_01184 | 1.6e-60 | clcA | P | chloride | ||
AEOOMBIJ_01185 | 8.8e-41 | clcA | P | chloride | ||
AEOOMBIJ_01186 | 9.7e-46 | oppA | E | ABC transporter substrate-binding protein | ||
AEOOMBIJ_01187 | 5.6e-132 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
AEOOMBIJ_01188 | 2.6e-172 | oppB | P | ABC transporter permease | ||
AEOOMBIJ_01189 | 1.5e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
AEOOMBIJ_01190 | 3.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
AEOOMBIJ_01191 | 4.9e-35 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
AEOOMBIJ_01192 | 3.7e-182 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
AEOOMBIJ_01193 | 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) | |
AEOOMBIJ_01194 | 7.6e-305 | yloV | S | DAK2 domain fusion protein YloV | ||
AEOOMBIJ_01195 | 1.5e-56 | asp | S | Asp23 family, cell envelope-related function | ||
AEOOMBIJ_01196 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
AEOOMBIJ_01197 | 1.4e-30 | |||||
AEOOMBIJ_01198 | 4.1e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
AEOOMBIJ_01199 | 2.9e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AEOOMBIJ_01200 | 4.5e-163 | 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 | |
AEOOMBIJ_01201 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
AEOOMBIJ_01202 | 1.1e-138 | stp | 3.1.3.16 | T | phosphatase | |
AEOOMBIJ_01203 | 1.6e-244 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
AEOOMBIJ_01204 | 2.1e-171 | 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 | |
AEOOMBIJ_01205 | 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 | ||
AEOOMBIJ_01206 | 1.1e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
AEOOMBIJ_01207 | 2.1e-111 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
AEOOMBIJ_01208 | 1.1e-77 | 6.3.3.2 | S | ASCH | ||
AEOOMBIJ_01209 | 2.6e-300 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AEOOMBIJ_01210 | 2.3e-153 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AEOOMBIJ_01211 | 1e-159 | 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 | |
AEOOMBIJ_01212 | 3.7e-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 | |
AEOOMBIJ_01213 | 2.9e-193 | 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 | |
AEOOMBIJ_01214 | 6.7e-156 | 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 | |
AEOOMBIJ_01215 | 1.1e-63 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
AEOOMBIJ_01216 | 3.4e-71 | yqhY | S | Asp23 family, cell envelope-related function | ||
AEOOMBIJ_01217 | 4.9e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
AEOOMBIJ_01218 | 1e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AEOOMBIJ_01219 | 1.3e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
AEOOMBIJ_01220 | 1.3e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
AEOOMBIJ_01221 | 3.7e-151 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
AEOOMBIJ_01222 | 7.8e-255 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AEOOMBIJ_01224 | 1.6e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
AEOOMBIJ_01225 | 4.3e-298 | S | Predicted membrane protein (DUF2207) | |||
AEOOMBIJ_01226 | 2.8e-157 | cinI | S | Serine hydrolase (FSH1) | ||
AEOOMBIJ_01227 | 1e-205 | M | Glycosyl hydrolases family 25 | |||
AEOOMBIJ_01228 | 2e-18 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
AEOOMBIJ_01229 | 2.9e-12 | |||||
AEOOMBIJ_01231 | 3.8e-15 | S | Domain of Unknown Function with PDB structure (DUF3850) | |||
AEOOMBIJ_01232 | 3.8e-125 | 1.3.5.4 | C | FAD binding domain | ||
AEOOMBIJ_01233 | 1.7e-213 | 1.3.5.4 | C | FAD binding domain | ||
AEOOMBIJ_01234 | 9.7e-83 | S | An automated process has identified a potential problem with this gene model | |||
AEOOMBIJ_01235 | 1e-137 | S | Protein of unknown function (DUF3100) | |||
AEOOMBIJ_01236 | 2.7e-246 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
AEOOMBIJ_01237 | 8.4e-229 | Q | Imidazolonepropionase and related amidohydrolases | |||
AEOOMBIJ_01238 | 0.0 | oppA | E | ABC transporter | ||
AEOOMBIJ_01239 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
AEOOMBIJ_01240 | 0.0 | mco | Q | Multicopper oxidase | ||
AEOOMBIJ_01241 | 1.9e-25 | |||||
AEOOMBIJ_01242 | 7.1e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
AEOOMBIJ_01243 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
AEOOMBIJ_01244 | 2e-61 | 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 | ||
AEOOMBIJ_01245 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AEOOMBIJ_01246 | 7.1e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AEOOMBIJ_01247 | 1e-156 | cjaA | ET | ABC transporter substrate-binding protein | ||
AEOOMBIJ_01248 | 1.5e-127 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AEOOMBIJ_01249 | 5.3e-116 | P | ABC transporter permease | |||
AEOOMBIJ_01250 | 9.1e-54 | papP | P | ABC transporter, permease protein | ||
AEOOMBIJ_01251 | 1.8e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
AEOOMBIJ_01252 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
AEOOMBIJ_01253 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
AEOOMBIJ_01254 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
AEOOMBIJ_01255 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
AEOOMBIJ_01256 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
AEOOMBIJ_01257 | 9e-223 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
AEOOMBIJ_01258 | 1.9e-236 | S | Peptidase M16 | |||
AEOOMBIJ_01259 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
AEOOMBIJ_01260 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
AEOOMBIJ_01261 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
AEOOMBIJ_01262 | 8.5e-196 | 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 | ||
AEOOMBIJ_01263 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
AEOOMBIJ_01264 | 1.9e-209 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
AEOOMBIJ_01265 | 2.5e-118 | yvyE | 3.4.13.9 | S | YigZ family | |
AEOOMBIJ_01266 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
AEOOMBIJ_01267 | 9.4e-132 | comFC | S | Competence protein | ||
AEOOMBIJ_01268 | 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 | |
AEOOMBIJ_01269 | 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 | |
AEOOMBIJ_01270 | 3.5e-109 | 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 | |
AEOOMBIJ_01271 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
AEOOMBIJ_01272 | 2.8e-35 | |||||
AEOOMBIJ_01274 | 3.8e-104 | pncA | Q | Isochorismatase family | ||
AEOOMBIJ_01275 | 4.9e-118 | |||||
AEOOMBIJ_01278 | 3.6e-63 | |||||
AEOOMBIJ_01279 | 1.4e-34 | |||||
AEOOMBIJ_01280 | 7.8e-10 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
AEOOMBIJ_01281 | 4.4e-35 | 3.6.3.2, 3.6.3.6 | P | cation transport ATPase | ||
AEOOMBIJ_01282 | 2.5e-264 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
AEOOMBIJ_01283 | 1.9e-19 | |||||
AEOOMBIJ_01284 | 2.9e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
AEOOMBIJ_01285 | 7.1e-46 | |||||
AEOOMBIJ_01286 | 3.1e-148 | glcU | U | sugar transport | ||
AEOOMBIJ_01287 | 3.7e-250 | lctP | C | L-lactate permease | ||
AEOOMBIJ_01288 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AEOOMBIJ_01289 | 6.4e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AEOOMBIJ_01290 | 8.8e-245 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AEOOMBIJ_01291 | 1.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AEOOMBIJ_01292 | 7.2e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
AEOOMBIJ_01293 | 9.1e-167 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
AEOOMBIJ_01294 | 1.6e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
AEOOMBIJ_01295 | 1.9e-118 | 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) | |
AEOOMBIJ_01296 | 1.5e-102 | GM | NmrA-like family | |||
AEOOMBIJ_01297 | 8.1e-87 | U | TraM recognition site of TraD and TraG | |||
AEOOMBIJ_01298 | 2.3e-32 | I | mechanosensitive ion channel activity | |||
AEOOMBIJ_01300 | 8.4e-15 | |||||
AEOOMBIJ_01301 | 2.4e-159 | trsE | S | COG0433 Predicted ATPase | ||
AEOOMBIJ_01302 | 9.4e-33 | M | Peptidase family M23 | |||
AEOOMBIJ_01305 | 3.4e-17 | CO | COG0526, thiol-disulfide isomerase and thioredoxins | |||
AEOOMBIJ_01309 | 5.7e-99 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
AEOOMBIJ_01310 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
AEOOMBIJ_01311 | 3.4e-42 | S | RloB-like protein | |||
AEOOMBIJ_01312 | 1.2e-164 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
AEOOMBIJ_01313 | 0.0 | hsdR | 3.1.21.3 | L | DEAD/DEAH box helicase | |
AEOOMBIJ_01314 | 0.0 | S | SLAP domain | |||
AEOOMBIJ_01316 | 1.1e-236 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
AEOOMBIJ_01317 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
AEOOMBIJ_01318 | 1.5e-239 | G | Bacterial extracellular solute-binding protein | |||
AEOOMBIJ_01319 | 5.7e-18 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)