ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
DDJEEEAA_00001 | 2.6e-07 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
DDJEEEAA_00002 | 1.3e-218 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
DDJEEEAA_00003 | 4.1e-175 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
DDJEEEAA_00004 | 4.9e-29 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
DDJEEEAA_00005 | 2e-151 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
DDJEEEAA_00006 | 1.3e-59 | arsC | 1.20.4.1 | T | Low molecular weight phosphatase family | |
DDJEEEAA_00007 | 4.1e-15 | ywzB | S | Protein of unknown function (DUF1146) | ||
DDJEEEAA_00008 | 9.3e-197 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
DDJEEEAA_00009 | 3.4e-167 | mbl | D | Cell shape determining protein MreB Mrl | ||
DDJEEEAA_00010 | 1.2e-26 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
DDJEEEAA_00011 | 1.8e-12 | S | Protein of unknown function (DUF2969) | |||
DDJEEEAA_00012 | 6.1e-187 | rodA | D | Belongs to the SEDS family | ||
DDJEEEAA_00013 | 2.7e-26 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
DDJEEEAA_00014 | 1.9e-171 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
DDJEEEAA_00015 | 1.3e-158 | ccpA | K | catabolite control protein A | ||
DDJEEEAA_00016 | 3.7e-42 | S | VanZ like family | |||
DDJEEEAA_00017 | 1.5e-119 | yebC | K | Transcriptional regulatory protein | ||
DDJEEEAA_00018 | 2.1e-102 | 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 | |
DDJEEEAA_00019 | 3.7e-16 | |||||
DDJEEEAA_00020 | 3.6e-112 | rssA | S | Phospholipase, patatin family | ||
DDJEEEAA_00021 | 1.5e-136 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
DDJEEEAA_00022 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
DDJEEEAA_00023 | 4.1e-296 | ydaO | E | amino acid | ||
DDJEEEAA_00024 | 1.6e-157 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
DDJEEEAA_00025 | 4.2e-128 | comFA | L | Helicase C-terminal domain protein | ||
DDJEEEAA_00026 | 5.7e-23 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
DDJEEEAA_00027 | 8.6e-60 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
DDJEEEAA_00029 | 3e-56 | sthIM | 2.1.1.72 | L | DNA methylase | |
DDJEEEAA_00030 | 1.8e-94 | sthIM | 2.1.1.72 | L | Adenine specific DNA methylase Mod | |
DDJEEEAA_00031 | 1e-155 | comEC | S | Competence protein ComEC | ||
DDJEEEAA_00032 | 2e-69 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
DDJEEEAA_00033 | 5.2e-50 | comEA | L | Competence protein ComEA | ||
DDJEEEAA_00034 | 4.7e-147 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
DDJEEEAA_00035 | 3.2e-66 | yrjD | S | LUD domain | ||
DDJEEEAA_00036 | 2.1e-245 | lutB | C | 4Fe-4S dicluster domain | ||
DDJEEEAA_00037 | 6.9e-117 | lutA | C | Cysteine-rich domain | ||
DDJEEEAA_00038 | 2.7e-48 | S | Domain of unknown function (DUF956) | |||
DDJEEEAA_00039 | 6.3e-115 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
DDJEEEAA_00040 | 7.2e-82 | 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 | ||
DDJEEEAA_00041 | 3.8e-105 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
DDJEEEAA_00042 | 5.1e-102 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
DDJEEEAA_00043 | 4.2e-49 | lytE | M | LysM domain protein | ||
DDJEEEAA_00044 | 1.4e-92 | T | Calcineurin-like phosphoesterase superfamily domain | |||
DDJEEEAA_00045 | 5.7e-85 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
DDJEEEAA_00047 | 4.4e-74 | draG | O | ADP-ribosylglycohydrolase | ||
DDJEEEAA_00048 | 8.9e-81 | 3.1.21.3 | V | type I restriction modification DNA specificity domain protein | ||
DDJEEEAA_00049 | 7.1e-86 | L | Belongs to the 'phage' integrase family | |||
DDJEEEAA_00050 | 1e-37 | L | Belongs to the 'phage' integrase family | |||
DDJEEEAA_00051 | 3.4e-61 | hsdS-1 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
DDJEEEAA_00052 | 4e-202 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
DDJEEEAA_00053 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
DDJEEEAA_00055 | 5.2e-81 | XK27_07525 | 3.6.1.55 | F | Hydrolase, nudix family | |
DDJEEEAA_00056 | 5.7e-57 | 3.6.1.27 | I | Acid phosphatase homologues | ||
DDJEEEAA_00057 | 1.8e-68 | maa | 2.3.1.79 | S | Maltose acetyltransferase | |
DDJEEEAA_00058 | 4.8e-73 | 2.3.1.178 | M | GNAT acetyltransferase | ||
DDJEEEAA_00060 | 1.4e-197 | ade | 3.5.4.2 | F | Adenine deaminase C-terminal domain | |
DDJEEEAA_00061 | 3.5e-65 | ypsA | S | Belongs to the UPF0398 family | ||
DDJEEEAA_00062 | 4e-83 | nhaC | C | Na H antiporter NhaC | ||
DDJEEEAA_00063 | 3.2e-93 | nhaC | C | Na H antiporter NhaC | ||
DDJEEEAA_00064 | 1.8e-76 | 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 | ||
DDJEEEAA_00065 | 1.1e-293 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
DDJEEEAA_00066 | 4.3e-113 | xerD | D | recombinase XerD | ||
DDJEEEAA_00067 | 6.9e-124 | cvfB | S | S1 domain | ||
DDJEEEAA_00068 | 4.1e-51 | yeaL | S | Protein of unknown function (DUF441) | ||
DDJEEEAA_00069 | 4.5e-58 | 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 | |||
DDJEEEAA_00070 | 5.8e-100 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
DDJEEEAA_00071 | 1.1e-56 | 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 | ||
DDJEEEAA_00072 | 7e-59 | 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 | ||
DDJEEEAA_00073 | 4.6e-37 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
DDJEEEAA_00074 | 7.8e-218 | 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 | ||
DDJEEEAA_00075 | 7e-79 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
DDJEEEAA_00076 | 6e-123 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
DDJEEEAA_00077 | 4.5e-179 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
DDJEEEAA_00078 | 1.2e-100 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
DDJEEEAA_00080 | 1.6e-42 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
DDJEEEAA_00081 | 1e-27 | ysxB | J | Cysteine protease Prp | ||
DDJEEEAA_00082 | 8.3e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
DDJEEEAA_00085 | 2.9e-08 | S | Protein of unknown function (DUF2922) | |||
DDJEEEAA_00087 | 1.3e-16 | K | DNA-templated transcription, initiation | |||
DDJEEEAA_00089 | 1.8e-14 | |||||
DDJEEEAA_00090 | 3e-87 | S | Haloacid dehalogenase-like hydrolase | |||
DDJEEEAA_00091 | 5.9e-39 | blpT | ||||
DDJEEEAA_00092 | 6.6e-19 | |||||
DDJEEEAA_00093 | 7.2e-08 | |||||
DDJEEEAA_00094 | 2.7e-171 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
DDJEEEAA_00095 | 2.2e-227 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
DDJEEEAA_00096 | 8.5e-36 | 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 | ||
DDJEEEAA_00098 | 6.2e-23 | K | Acetyltransferase (GNAT) domain | |||
DDJEEEAA_00099 | 3.2e-214 | yjeM | E | Amino Acid | ||
DDJEEEAA_00100 | 1.6e-189 | glnPH2 | P | ABC transporter permease | ||
DDJEEEAA_00101 | 8.8e-112 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DDJEEEAA_00102 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
DDJEEEAA_00103 | 1.5e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
DDJEEEAA_00104 | 1.3e-62 | S | Glycosyltransferase like family 2 | |||
DDJEEEAA_00105 | 4.3e-137 | tetA | EGP | Major facilitator Superfamily | ||
DDJEEEAA_00106 | 1.8e-32 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
DDJEEEAA_00107 | 1.9e-67 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
DDJEEEAA_00108 | 2.4e-157 | XK27_09615 | S | reductase | ||
DDJEEEAA_00109 | 7.5e-39 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
DDJEEEAA_00110 | 1.8e-135 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)