| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| EMMAEGCE_00001 | 6.4e-301 | I | Protein of unknown function (DUF2974) | |||
| EMMAEGCE_00002 | 4.6e-105 | 3.6.1.55 | F | NUDIX domain | ||
| EMMAEGCE_00003 | 5.3e-206 | pbpX1 | V | Beta-lactamase | ||
| EMMAEGCE_00004 | 1e-198 | 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 | |
| EMMAEGCE_00005 | 7.1e-217 | aspC | 2.6.1.1 | E | Aminotransferase | |
| EMMAEGCE_00006 | 5.4e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
| EMMAEGCE_00007 | 1.1e-175 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
| EMMAEGCE_00008 | 2.1e-221 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
| EMMAEGCE_00009 | 3.6e-78 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
| EMMAEGCE_00010 | 9.4e-250 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
| EMMAEGCE_00011 | 4.1e-264 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
| EMMAEGCE_00012 | 4.4e-191 | 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 | |
| EMMAEGCE_00013 | 1.1e-153 | yjeM | E | Amino Acid | ||
| EMMAEGCE_00014 | 2e-44 | yjeM | E | Amino Acid | ||
| EMMAEGCE_00015 | 1.3e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
| EMMAEGCE_00016 | 1.3e-235 | 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 | ||
| EMMAEGCE_00017 | 4.2e-213 | 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 | ||
| EMMAEGCE_00018 | 3.3e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
| EMMAEGCE_00019 | 1.3e-151 | |||||
| EMMAEGCE_00020 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
| EMMAEGCE_00021 | 7e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
| EMMAEGCE_00022 | 1.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
| EMMAEGCE_00023 | 4.8e-174 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
| EMMAEGCE_00024 | 0.0 | comEC | S | Competence protein ComEC | ||
| EMMAEGCE_00025 | 1.9e-84 | comEA | L | Competence protein ComEA | ||
| EMMAEGCE_00026 | 5.4e-192 | ylbL | T | Belongs to the peptidase S16 family | ||
| EMMAEGCE_00027 | 1.6e-85 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
| EMMAEGCE_00028 | 2.2e-96 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
| EMMAEGCE_00029 | 3.3e-53 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
| EMMAEGCE_00030 | 4.7e-208 | ftsW | D | Belongs to the SEDS family | ||
| EMMAEGCE_00031 | 0.0 | typA | T | GTP-binding protein TypA | ||
| EMMAEGCE_00032 | 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 | |
| EMMAEGCE_00033 | 4.2e-33 | ykzG | S | Belongs to the UPF0356 family | ||
| EMMAEGCE_00034 | 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 | ||
| EMMAEGCE_00035 | 2.3e-29 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| EMMAEGCE_00036 | 1.6e-36 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| EMMAEGCE_00037 | 2.9e-82 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| EMMAEGCE_00038 | 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 | |
| EMMAEGCE_00039 | 2e-104 | S | Repeat protein | |||
| EMMAEGCE_00040 | 5.6e-126 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
| EMMAEGCE_00041 | 1.2e-221 | 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 | |
| EMMAEGCE_00042 | 1.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
| EMMAEGCE_00043 | 2.4e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
| EMMAEGCE_00044 | 8.5e-125 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
| EMMAEGCE_00045 | 1.6e-38 | |||||
| EMMAEGCE_00046 | 4.4e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
| EMMAEGCE_00047 | 2.1e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
| EMMAEGCE_00048 | 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) | |
| EMMAEGCE_00049 | 1.5e-101 | gpsB | D | DivIVA domain protein | ||
| EMMAEGCE_00050 | 3.7e-148 | ylmH | S | S4 domain protein | ||
| EMMAEGCE_00051 | 9e-47 | yggT | S | YGGT family | ||
| EMMAEGCE_00052 | 2.1e-73 | 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 | ||
| EMMAEGCE_00053 | 2.6e-207 | 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 | ||
| EMMAEGCE_00054 | 1.2e-231 | 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 | ||
| EMMAEGCE_00055 | 2.9e-151 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
| EMMAEGCE_00056 | 5.2e-209 | 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) |
| EMMAEGCE_00057 | 1.5e-258 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
| EMMAEGCE_00058 | 7.1e-178 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
| EMMAEGCE_00059 | 3.3e-47 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
| EMMAEGCE_00060 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
| EMMAEGCE_00061 | 2.4e-54 | ftsL | D | Cell division protein FtsL | ||
| EMMAEGCE_00062 | 1.5e-183 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
| EMMAEGCE_00063 | 2.5e-33 | mraZ | K | Belongs to the MraZ family | ||
| EMMAEGCE_00064 | 1e-19 | mraZ | K | Belongs to the MraZ family | ||
| EMMAEGCE_00065 | 2.2e-54 | S | Protein of unknown function (DUF3397) | |||
| EMMAEGCE_00066 | 6.5e-13 | S | Protein of unknown function (DUF4044) | |||
| EMMAEGCE_00067 | 4.5e-97 | mreD | ||||
| EMMAEGCE_00068 | 1e-148 | mreC | M | Involved in formation and maintenance of cell shape | ||
| EMMAEGCE_00069 | 6.4e-174 | mreB | D | cell shape determining protein MreB | ||
| EMMAEGCE_00070 | 2.1e-114 | radC | L | DNA repair protein | ||
| EMMAEGCE_00071 | 1.3e-125 | S | Haloacid dehalogenase-like hydrolase | |||
| EMMAEGCE_00072 | 7.2e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
| EMMAEGCE_00073 | 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 | |
| EMMAEGCE_00074 | 8.3e-82 | ydiM | G | Major Facilitator Superfamily | ||
| EMMAEGCE_00075 | 3.6e-137 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
| EMMAEGCE_00076 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
| EMMAEGCE_00077 | 1.3e-84 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
| EMMAEGCE_00078 | 4.3e-219 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
| EMMAEGCE_00079 | 1.1e-132 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
| EMMAEGCE_00080 | 1.3e-38 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| EMMAEGCE_00081 | 8.8e-127 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| EMMAEGCE_00082 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| EMMAEGCE_00083 | 2.4e-275 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
| EMMAEGCE_00084 | 1.1e-200 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
| EMMAEGCE_00085 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
| EMMAEGCE_00086 | 4.3e-244 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
| EMMAEGCE_00087 | 9.9e-122 | K | SIS domain | |||
| EMMAEGCE_00088 | 4.4e-164 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
| EMMAEGCE_00089 | 1.5e-65 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
| EMMAEGCE_00090 | 1.3e-113 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
| EMMAEGCE_00091 | 8.1e-285 | xylG | 3.6.3.17 | S | ABC transporter | |
| EMMAEGCE_00092 | 7.2e-171 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
| EMMAEGCE_00093 | 4e-13 | S | Uncharacterised protein family (UPF0236) | |||
| EMMAEGCE_00094 | 2.4e-73 | S | Uncharacterised protein family (UPF0236) | |||
| EMMAEGCE_00095 | 1.2e-81 | S | Uncharacterised protein family (UPF0236) | |||
| EMMAEGCE_00096 | 6.1e-219 | naiP | EGP | Major facilitator Superfamily | ||
| EMMAEGCE_00097 | 0.0 | XK27_00340 | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
| EMMAEGCE_00098 | 1.6e-135 | oppA | E | ABC transporter | ||
| EMMAEGCE_00099 | 6.9e-62 | oppA | E | ABC transporter | ||
| EMMAEGCE_00100 | 5e-96 | Q | Imidazolonepropionase and related amidohydrolases |
Showing 1 to 100 of 1,844 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)