ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
BNDDKGJP_00001 | 9.1e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
BNDDKGJP_00002 | 3.2e-181 | ccpA | K | catabolite control protein A | ||
BNDDKGJP_00003 | 2.6e-266 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
BNDDKGJP_00004 | 4.3e-55 | |||||
BNDDKGJP_00005 | 1.2e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
BNDDKGJP_00006 | 8.3e-105 | yutD | S | Protein of unknown function (DUF1027) | ||
BNDDKGJP_00007 | 6.9e-144 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
BNDDKGJP_00008 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
BNDDKGJP_00009 | 2.3e-116 | dedA | S | SNARE-like domain protein | ||
BNDDKGJP_00010 | 8e-185 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
BNDDKGJP_00011 | 7.1e-63 | M | LysM domain protein | |||
BNDDKGJP_00012 | 4.1e-101 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
BNDDKGJP_00013 | 3.7e-243 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
BNDDKGJP_00014 | 5e-48 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BNDDKGJP_00015 | 6.9e-116 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
BNDDKGJP_00016 | 9.7e-52 | S | Iron-sulfur cluster assembly protein | |||
BNDDKGJP_00017 | 3.8e-154 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
BNDDKGJP_00018 | 1.3e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
BNDDKGJP_00019 | 2.4e-44 | |||||
BNDDKGJP_00020 | 2.1e-285 | lsa | S | ABC transporter | ||
BNDDKGJP_00021 | 1.1e-08 | |||||
BNDDKGJP_00022 | 1.7e-125 | Z012_12235 | S | Baseplate J-like protein | ||
BNDDKGJP_00023 | 9.5e-33 | |||||
BNDDKGJP_00024 | 1.2e-48 | |||||
BNDDKGJP_00025 | 5.7e-104 | |||||
BNDDKGJP_00026 | 1.4e-45 | |||||
BNDDKGJP_00027 | 1.2e-58 | M | LysM domain | |||
BNDDKGJP_00028 | 0.0 | 3.4.14.13 | M | Phage tail tape measure protein TP901 | ||
BNDDKGJP_00030 | 9e-27 | |||||
BNDDKGJP_00031 | 4e-56 | |||||
BNDDKGJP_00032 | 9.7e-153 | Z012_02110 | S | Protein of unknown function (DUF3383) | ||
BNDDKGJP_00033 | 8e-57 | |||||
BNDDKGJP_00034 | 2.9e-45 | |||||
BNDDKGJP_00035 | 1.5e-75 | |||||
BNDDKGJP_00036 | 2.1e-30 | S | Protein of unknown function (DUF4054) | |||
BNDDKGJP_00037 | 3.5e-142 | Z012_11565 | S | Uncharacterized protein conserved in bacteria (DUF2184) | ||
BNDDKGJP_00038 | 9.2e-59 | |||||
BNDDKGJP_00039 | 1.1e-86 | S | Uncharacterized protein conserved in bacteria (DUF2213) | |||
BNDDKGJP_00040 | 1.1e-07 | S | Lysin motif | |||
BNDDKGJP_00041 | 1e-97 | S | Phage Mu protein F like protein | |||
BNDDKGJP_00042 | 7e-142 | S | Protein of unknown function (DUF1073) | |||
BNDDKGJP_00043 | 1.8e-230 | S | Terminase-like family | |||
BNDDKGJP_00044 | 1.5e-28 | L | Terminase small subunit | |||
BNDDKGJP_00045 | 5.2e-10 | hicA | N | HicA toxin of bacterial toxin-antitoxin, | ||
BNDDKGJP_00046 | 2.7e-35 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
BNDDKGJP_00054 | 1.2e-14 | |||||
BNDDKGJP_00055 | 1.2e-40 | rusA | 3.1.22.4 | L | Endodeoxyribonuclease RusA | |
BNDDKGJP_00061 | 1.4e-51 | dnaC | L | IstB-like ATP binding protein | ||
BNDDKGJP_00062 | 6.8e-33 | S | Conserved phage C-terminus (Phg_2220_C) | |||
BNDDKGJP_00063 | 6.9e-59 | S | Protein of unknown function (DUF1071) | |||
BNDDKGJP_00069 | 3.6e-09 | |||||
BNDDKGJP_00074 | 8e-97 | S | AntA/AntB antirepressor | |||
BNDDKGJP_00075 | 2.9e-12 | |||||
BNDDKGJP_00080 | 2.1e-76 | S | Phage antirepressor protein KilAC domain | |||
BNDDKGJP_00081 | 1.8e-10 | |||||
BNDDKGJP_00082 | 1.1e-12 | |||||
BNDDKGJP_00083 | 3.5e-15 | ansR | 3.4.21.88 | K | Cro/C1-type HTH DNA-binding domain | |
BNDDKGJP_00084 | 1.2e-10 | E | Zn peptidase | |||
BNDDKGJP_00085 | 6e-14 | |||||
BNDDKGJP_00089 | 1.6e-20 | S | YjcQ protein | |||
BNDDKGJP_00090 | 4.2e-180 | sip | L | Belongs to the 'phage' integrase family | ||
BNDDKGJP_00091 | 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 | ||
BNDDKGJP_00092 | 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 | ||
BNDDKGJP_00093 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
BNDDKGJP_00094 | 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 | ||
BNDDKGJP_00095 | 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 | ||
BNDDKGJP_00096 | 3.2e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
BNDDKGJP_00097 | 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 | |
BNDDKGJP_00098 | 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 | ||
BNDDKGJP_00099 | 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 | ||
BNDDKGJP_00100 | 3.2e-47 | rplGA | J | ribosomal protein | ||
BNDDKGJP_00101 | 8.8e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
BNDDKGJP_00102 | 1.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
BNDDKGJP_00103 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
BNDDKGJP_00104 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
BNDDKGJP_00105 | 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 | |
BNDDKGJP_00106 | 5.7e-196 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
BNDDKGJP_00107 | 8.4e-140 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
BNDDKGJP_00108 | 5.4e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
BNDDKGJP_00109 | 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 | ||
BNDDKGJP_00110 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
BNDDKGJP_00111 | 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 | ||
BNDDKGJP_00112 | 3.7e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
BNDDKGJP_00113 | 3e-195 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
BNDDKGJP_00114 | 2.9e-116 | plsC | 2.3.1.51 | I | Acyltransferase | |
BNDDKGJP_00115 | 3.9e-223 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
BNDDKGJP_00116 | 1.2e-145 | V | ABC transporter, ATP-binding protein | |||
BNDDKGJP_00117 | 4.2e-144 | V | ABC transporter, ATP-binding protein | |||
BNDDKGJP_00118 | 0.0 | V | ABC transporter | |||
BNDDKGJP_00120 | 9.6e-121 | K | response regulator | |||
BNDDKGJP_00121 | 6.6e-207 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
BNDDKGJP_00122 | 5.5e-305 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
BNDDKGJP_00123 | 8e-145 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
BNDDKGJP_00124 | 1.4e-53 | S | Enterocin A Immunity | |||
BNDDKGJP_00125 | 2.5e-33 | |||||
BNDDKGJP_00126 | 9.5e-26 | |||||
BNDDKGJP_00127 | 1e-24 | |||||
BNDDKGJP_00128 | 3e-270 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
BNDDKGJP_00129 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
BNDDKGJP_00130 | 2.1e-255 | S | Archaea bacterial proteins of unknown function |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)