| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| FDLLKGPL_00001 | 7.4e-177 | 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 | |
| FDLLKGPL_00002 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
| FDLLKGPL_00003 | 2.4e-192 | cycA | E | Amino acid permease | ||
| FDLLKGPL_00004 | 6.4e-187 | ytgP | S | Polysaccharide biosynthesis protein | ||
| FDLLKGPL_00005 | 4e-61 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
| FDLLKGPL_00006 | 1.2e-80 | 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 | |
| FDLLKGPL_00007 | 3e-193 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
| FDLLKGPL_00009 | 5.2e-36 | |||||
| FDLLKGPL_00010 | 3.4e-66 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
| FDLLKGPL_00011 | 4.2e-61 | marR | K | Transcriptional regulator, MarR family | ||
| FDLLKGPL_00012 | 2.9e-102 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
| FDLLKGPL_00013 | 2.2e-27 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
| FDLLKGPL_00014 | 2.9e-104 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
| FDLLKGPL_00015 | 1.1e-98 | IQ | reductase | |||
| FDLLKGPL_00016 | 2.1e-195 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
| FDLLKGPL_00017 | 4.6e-47 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
| FDLLKGPL_00018 | 3.9e-64 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
| FDLLKGPL_00019 | 9.3e-216 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
| FDLLKGPL_00020 | 2.7e-125 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
| FDLLKGPL_00021 | 4.4e-101 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
| FDLLKGPL_00022 | 5.5e-109 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
| FDLLKGPL_00023 | 5.1e-231 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
| FDLLKGPL_00024 | 3.1e-240 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
| FDLLKGPL_00025 | 2.3e-301 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
| FDLLKGPL_00026 | 5.7e-119 | gla | U | Major intrinsic protein | ||
| FDLLKGPL_00027 | 5.8e-45 | ykuL | S | CBS domain | ||
| FDLLKGPL_00028 | 3.9e-61 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
| FDLLKGPL_00029 | 2.1e-176 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
| FDLLKGPL_00030 | 9e-87 | ykuT | M | mechanosensitive ion channel | ||
| FDLLKGPL_00032 | 3e-285 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
| FDLLKGPL_00033 | 2e-21 | yheA | S | Belongs to the UPF0342 family | ||
| FDLLKGPL_00034 | 9.5e-127 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
| FDLLKGPL_00035 | 3.3e-113 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
| FDLLKGPL_00037 | 7e-53 | hit | FG | histidine triad | ||
| FDLLKGPL_00038 | 1.3e-94 | ecsA | V | ABC transporter, ATP-binding protein | ||
| FDLLKGPL_00039 | 4.9e-72 | ecsB | U | ABC transporter | ||
| FDLLKGPL_00040 | 1.6e-98 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
| FDLLKGPL_00041 | 3.9e-100 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
| FDLLKGPL_00043 | 4e-45 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
| FDLLKGPL_00044 | 4e-76 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
| FDLLKGPL_00045 | 1.2e-239 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
| FDLLKGPL_00046 | 7.6e-223 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
| FDLLKGPL_00047 | 2.5e-61 | phaJ | I | N-terminal half of MaoC dehydratase | ||
| FDLLKGPL_00048 | 6.7e-69 | ybhL | S | Belongs to the BI1 family | ||
| FDLLKGPL_00049 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
| FDLLKGPL_00050 | 4.3e-107 | 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 | |
| FDLLKGPL_00051 | 1.6e-50 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
| FDLLKGPL_00052 | 6.1e-66 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
| FDLLKGPL_00053 | 1.4e-78 | dnaB | L | replication initiation and membrane attachment | ||
| FDLLKGPL_00054 | 1.3e-107 | dnaI | L | Primosomal protein DnaI | ||
| FDLLKGPL_00055 | 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) | |
| FDLLKGPL_00056 | 1.3e-79 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
| FDLLKGPL_00057 | 1.4e-24 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
| FDLLKGPL_00058 | 2.2e-52 | 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 | ||
| FDLLKGPL_00059 | 1.2e-70 | yqeG | S | HAD phosphatase, family IIIA | ||
| FDLLKGPL_00060 | 6.7e-180 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
| FDLLKGPL_00061 | 6e-30 | yhbY | J | RNA-binding protein | ||
| FDLLKGPL_00062 | 3.5e-77 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
| FDLLKGPL_00063 | 2.6e-69 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
| FDLLKGPL_00064 | 1.5e-48 | 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 | ||
| FDLLKGPL_00065 | 1.5e-82 | H | Nodulation protein S (NodS) | |||
| FDLLKGPL_00066 | 1e-122 | ylbM | S | Belongs to the UPF0348 family | ||
| FDLLKGPL_00067 | 2e-57 | yceD | S | Uncharacterized ACR, COG1399 | ||
| FDLLKGPL_00068 | 1.9e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
| FDLLKGPL_00069 | 4e-89 | plsC | 2.3.1.51 | I | Acyltransferase | |
| FDLLKGPL_00070 | 8.5e-94 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
| FDLLKGPL_00071 | 1.5e-27 | yazA | L | GIY-YIG catalytic domain protein | ||
| FDLLKGPL_00072 | 1.9e-128 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
| FDLLKGPL_00073 | 8.8e-127 | 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 | ||
| FDLLKGPL_00074 | 6.9e-37 | |||||
| FDLLKGPL_00075 | 3.4e-92 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
| FDLLKGPL_00076 | 1.4e-57 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
| FDLLKGPL_00077 | 7.9e-157 | 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) | |
| FDLLKGPL_00078 | 9.3e-226 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
| FDLLKGPL_00079 | 6.6e-107 | pacA | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
| FDLLKGPL_00081 | 3.1e-111 | K | response regulator | |||
| FDLLKGPL_00082 | 3.9e-167 | arlS | 2.7.13.3 | T | Histidine kinase | |
| FDLLKGPL_00083 | 5.1e-117 | 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 | ||
| FDLLKGPL_00084 | 1.6e-23 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
| FDLLKGPL_00085 | 4.7e-136 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
| FDLLKGPL_00086 | 7.3e-105 | |||||
| FDLLKGPL_00087 | 5.5e-117 | |||||
| FDLLKGPL_00088 | 1.3e-41 | dut | S | dUTPase | ||
| FDLLKGPL_00089 | 2.1e-94 | 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 | ||
| FDLLKGPL_00090 | 3.7e-46 | yqhY | S | Asp23 family, cell envelope-related function | ||
| FDLLKGPL_00091 | 5.5e-36 | 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 | ||
| FDLLKGPL_00092 | 1e-103 | 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 | |
| FDLLKGPL_00093 | 9.9e-146 | 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 | |
| FDLLKGPL_00094 | 9.6e-17 | 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 | |
| FDLLKGPL_00095 | 1.6e-83 | 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 | |
| FDLLKGPL_00096 | 1.2e-120 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
| FDLLKGPL_00097 | 6.6e-49 | argR | K | Regulates arginine biosynthesis genes | ||
| FDLLKGPL_00098 | 8.7e-176 | recN | L | May be involved in recombinational repair of damaged DNA | ||
| FDLLKGPL_00099 | 2.5e-83 | 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 | |
| FDLLKGPL_00100 | 2.2e-30 | ynzC | S | UPF0291 protein | ||
| FDLLKGPL_00101 | 2.9e-26 | yneF | S | UPF0154 protein | ||
| FDLLKGPL_00102 | 1.6e-92 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
| FDLLKGPL_00103 | 2.1e-43 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
| FDLLKGPL_00104 | 2.5e-75 | yciQ | P | membrane protein (DUF2207) | ||
| FDLLKGPL_00105 | 1.7e-19 | D | nuclear chromosome segregation |
Showing 1 to 100 of 1,719 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)