ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HNLDEPFJ_00001 | 1.4e-299 | dnaK | O | Heat shock 70 kDa protein | ||
HNLDEPFJ_00002 | 7e-63 | 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 | ||
HNLDEPFJ_00003 | 3.7e-185 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
HNLDEPFJ_00004 | 1.4e-99 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
HNLDEPFJ_00005 | 3.1e-139 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
HNLDEPFJ_00006 | 2.8e-131 | ais | G | Phosphoglycerate mutase | ||
HNLDEPFJ_00007 | 6.6e-243 | XK27_08635 | S | UPF0210 protein | ||
HNLDEPFJ_00008 | 6.1e-39 | gcvR | T | UPF0237 protein | ||
HNLDEPFJ_00009 | 2.1e-179 | capA | M | Bacterial capsule synthesis protein | ||
HNLDEPFJ_00010 | 1.7e-139 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNLDEPFJ_00011 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNLDEPFJ_00012 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNLDEPFJ_00013 | 5.8e-158 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
HNLDEPFJ_00014 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
HNLDEPFJ_00015 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
HNLDEPFJ_00016 | 3e-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 | |
HNLDEPFJ_00017 | 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 | ||
HNLDEPFJ_00018 | 2.2e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
HNLDEPFJ_00019 | 3e-60 | divIC | D | Septum formation initiator | ||
HNLDEPFJ_00021 | 1.2e-18 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
HNLDEPFJ_00022 | 7.1e-106 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
HNLDEPFJ_00023 | 1.5e-101 | 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 | |
HNLDEPFJ_00025 | 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 | ||
HNLDEPFJ_00027 | 8.4e-70 | K | LytTr DNA-binding domain | |||
HNLDEPFJ_00028 | 1e-78 | S | Protein of unknown function (DUF3021) | |||
HNLDEPFJ_00029 | 1.4e-234 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
HNLDEPFJ_00030 | 6.1e-211 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
HNLDEPFJ_00031 | 6.1e-99 | metI | P | ABC transporter (Permease | ||
HNLDEPFJ_00032 | 7e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
HNLDEPFJ_00033 | 5.9e-263 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
HNLDEPFJ_00034 | 1.1e-158 | metQ | M | Belongs to the NlpA lipoprotein family | ||
HNLDEPFJ_00035 | 9.3e-92 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
HNLDEPFJ_00036 | 7.3e-50 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
HNLDEPFJ_00037 | 9.1e-234 | sufD | O | assembly protein SufD | ||
HNLDEPFJ_00038 | 1.7e-137 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
HNLDEPFJ_00039 | 3e-183 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
HNLDEPFJ_00040 | 1.2e-124 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
HNLDEPFJ_00041 | 6.3e-18 | S | Protein of unknown function (DUF3021) | |||
HNLDEPFJ_00042 | 2e-277 | 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 | ||
HNLDEPFJ_00043 | 1.1e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HNLDEPFJ_00044 | 4.2e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
HNLDEPFJ_00045 | 3.4e-61 | 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 | |
HNLDEPFJ_00046 | 3.2e-182 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
HNLDEPFJ_00048 | 3.2e-95 | S | reductase | |||
HNLDEPFJ_00049 | 3.9e-72 | badR | K | Transcriptional regulator, marr family | ||
HNLDEPFJ_00050 | 5.5e-36 | XK27_02060 | S | Transglycosylase associated protein | ||
HNLDEPFJ_00051 | 5.6e-236 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
HNLDEPFJ_00052 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
HNLDEPFJ_00053 | 7.5e-14 | |||||
HNLDEPFJ_00054 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
HNLDEPFJ_00055 | 8.3e-296 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
HNLDEPFJ_00056 | 3.2e-44 | yrzB | S | Belongs to the UPF0473 family | ||
HNLDEPFJ_00057 | 1.8e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
HNLDEPFJ_00058 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
HNLDEPFJ_00059 | 4.2e-217 | araT | 2.6.1.1 | E | Aminotransferase | |
HNLDEPFJ_00060 | 2.7e-140 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
HNLDEPFJ_00061 | 4.6e-183 | 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 | |
HNLDEPFJ_00062 | 8.1e-30 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
HNLDEPFJ_00063 | 8.9e-130 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
HNLDEPFJ_00064 | 5.7e-183 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
HNLDEPFJ_00065 | 2.5e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
HNLDEPFJ_00066 | 3.3e-33 | |||||
HNLDEPFJ_00067 | 1.6e-174 | 1.1.1.169 | H | Ketopantoate reductase | ||
HNLDEPFJ_00068 | 2e-135 | 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) | |
HNLDEPFJ_00069 | 3.3e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
HNLDEPFJ_00070 | 2.3e-139 | S | SseB protein N-terminal domain | |||
HNLDEPFJ_00071 | 1.2e-236 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
HNLDEPFJ_00072 | 8.2e-116 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
HNLDEPFJ_00073 | 1.6e-123 | yaaA | S | Belongs to the UPF0246 family | ||
HNLDEPFJ_00074 | 3.2e-167 | XK27_01785 | S | cog cog1284 | ||
HNLDEPFJ_00075 | 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) | |
HNLDEPFJ_00077 | 8.1e-85 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
HNLDEPFJ_00078 | 1.5e-236 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
HNLDEPFJ_00079 | 3.3e-112 | 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 | |
HNLDEPFJ_00080 | 1.3e-111 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
HNLDEPFJ_00081 | 1.4e-193 | yhjX | P | Major Facilitator | ||
HNLDEPFJ_00082 | 4.8e-85 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
HNLDEPFJ_00083 | 5.1e-205 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
HNLDEPFJ_00084 | 1.7e-134 | parB | K | Belongs to the ParB family | ||
HNLDEPFJ_00085 | 9.6e-23 | |||||
HNLDEPFJ_00086 | 2.3e-256 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HNLDEPFJ_00087 | 2e-88 | XK27_09675 | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
HNLDEPFJ_00088 | 4.3e-158 | 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 | ||
HNLDEPFJ_00089 | 2.8e-182 | 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 | ||
HNLDEPFJ_00090 | 3.5e-71 | adcR | K | transcriptional | ||
HNLDEPFJ_00091 | 8.3e-136 | adcC | P | ABC transporter, ATP-binding protein | ||
HNLDEPFJ_00092 | 8.7e-129 | adcB | P | ABC transporter (Permease | ||
HNLDEPFJ_00093 | 1.6e-230 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
HNLDEPFJ_00094 | 1.6e-143 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
HNLDEPFJ_00095 | 5.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
HNLDEPFJ_00096 | 7.7e-47 | yajC | U | protein transport | ||
HNLDEPFJ_00097 | 1.9e-66 | yeeN | K | transcriptional regulatory protein | ||
HNLDEPFJ_00098 | 1.9e-23 | rpmD | J | Ribosomal protein L30p/L7e | ||
HNLDEPFJ_00099 | 1.3e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
HNLDEPFJ_00100 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
HNLDEPFJ_00101 | 6.6e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
HNLDEPFJ_00102 | 1.2e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
HNLDEPFJ_00103 | 1.5e-28 | 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 | ||
HNLDEPFJ_00104 | 1.3e-80 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
HNLDEPFJ_00105 | 1.1e-50 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HNLDEPFJ_00106 | 1.7e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
HNLDEPFJ_00107 | 1.7e-205 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
HNLDEPFJ_00108 | 5.9e-82 | nrdI | F | Belongs to the NrdI family | ||
HNLDEPFJ_00109 | 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 | |
HNLDEPFJ_00111 | 7.2e-221 | 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 | |
HNLDEPFJ_00112 | 1.1e-184 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
HNLDEPFJ_00113 | 1e-27 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
HNLDEPFJ_00114 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
HNLDEPFJ_00116 | 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 | ||
HNLDEPFJ_00117 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
HNLDEPFJ_00118 | 1e-204 | tilS | 2.4.2.8, 6.3.4.19 | D | 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 | |
HNLDEPFJ_00119 | 1.1e-272 | 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) | |
HNLDEPFJ_00120 | 2.8e-263 | 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) | |
HNLDEPFJ_00121 | 1.5e-46 | 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) | |
HNLDEPFJ_00122 | 1.2e-40 | tagE | 2.4.1.52 | GT4 | M | transferase activity, transferring glycosyl groups |
HNLDEPFJ_00123 | 4.2e-17 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
HNLDEPFJ_00124 | 1.5e-91 | 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 | ||
HNLDEPFJ_00125 | 2.4e-142 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNLDEPFJ_00126 | 7e-238 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNLDEPFJ_00127 | 1.1e-214 | pepC | 3.4.22.40 | E | aminopeptidase | |
HNLDEPFJ_00128 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
HNLDEPFJ_00129 | 3.9e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
HNLDEPFJ_00130 | 3e-69 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
HNLDEPFJ_00131 | 7.8e-52 | purR | 2.4.2.22, 2.4.2.7 | F | operon repressor | |
HNLDEPFJ_00132 | 1.8e-21 | 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 | ||
HNLDEPFJ_00133 | 2.4e-220 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
HNLDEPFJ_00134 | 6.4e-91 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
HNLDEPFJ_00135 | 1.4e-174 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
HNLDEPFJ_00136 | 1.1e-84 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
HNLDEPFJ_00137 | 6.1e-83 | mreD | M | rod shape-determining protein MreD | ||
HNLDEPFJ_00138 | 6.6e-92 | mreC | M | Involved in formation and maintenance of cell shape | ||
HNLDEPFJ_00139 | 4.9e-27 | S | membrane | |||
HNLDEPFJ_00140 | 3.7e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
HNLDEPFJ_00141 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
HNLDEPFJ_00142 | 4.7e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
HNLDEPFJ_00143 | 2.4e-207 | rny | D | Endoribonuclease that initiates mRNA decay | ||
HNLDEPFJ_00144 | 9.1e-125 | fruR | K | transcriptional | ||
HNLDEPFJ_00145 | 5.4e-60 | D | nuclear chromosome segregation | |||
HNLDEPFJ_00146 | 2.2e-123 | glnQ | E | abc transporter atp-binding protein | ||
HNLDEPFJ_00147 | 4.2e-273 | glnP | P | ABC transporter | ||
HNLDEPFJ_00148 | 1.1e-42 | ygaC | J | Belongs to the UPF0374 family | ||
HNLDEPFJ_00149 | 2.9e-54 | ygaC | J | Belongs to the UPF0374 family | ||
HNLDEPFJ_00150 | 2.2e-137 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
HNLDEPFJ_00151 | 7.7e-247 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
HNLDEPFJ_00152 | 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 | |
HNLDEPFJ_00153 | 6.1e-140 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
HNLDEPFJ_00154 | 3.8e-134 | 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) | |
HNLDEPFJ_00155 | 7.7e-91 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
HNLDEPFJ_00156 | 3.6e-160 | rsgA | 3.1.3.100 | G | 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 | |
HNLDEPFJ_00158 | 1.2e-155 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
HNLDEPFJ_00159 | 1.1e-98 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
HNLDEPFJ_00160 | 9.4e-89 | tatD | L | Hydrolase, tatd | ||
HNLDEPFJ_00161 | 3.1e-178 | cbf | S | 3'-5' exoribonuclease yhaM | ||
HNLDEPFJ_00162 | 1.4e-170 | rmuC | S | RmuC domain protein | ||
HNLDEPFJ_00163 | 2.9e-116 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
HNLDEPFJ_00164 | 1.1e-58 | rplO | J | binds to the 23S rRNA | ||
HNLDEPFJ_00165 | 2.1e-230 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
HNLDEPFJ_00166 | 7.3e-118 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
HNLDEPFJ_00167 | 2.7e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
HNLDEPFJ_00168 | 7.8e-15 | rpmJ | J | Ribosomal protein L36 | ||
HNLDEPFJ_00169 | 1.4e-96 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
HNLDEPFJ_00170 | 3.7e-185 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
HNLDEPFJ_00171 | 1.5e-225 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
HNLDEPFJ_00172 | 7.3e-141 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
HNLDEPFJ_00173 | 2.4e-100 | S | CAAX amino terminal protease family protein | |||
HNLDEPFJ_00174 | 5.2e-131 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
HNLDEPFJ_00175 | 1.8e-203 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
HNLDEPFJ_00176 | 3.5e-08 | XK27_10305 | S | Domain of unknown function (DUF4651) | ||
HNLDEPFJ_00177 | 1.4e-41 | ylxQ | J | ribosomal protein | ||
HNLDEPFJ_00178 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
HNLDEPFJ_00179 | 8.4e-81 | nusA | K | Participates in both transcription termination and antitermination | ||
HNLDEPFJ_00180 | 1.4e-83 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
HNLDEPFJ_00181 | 1.7e-309 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
HNLDEPFJ_00182 | 1.3e-70 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
HNLDEPFJ_00183 | 5.9e-09 | 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 | ||
HNLDEPFJ_00184 | 2.4e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HNLDEPFJ_00185 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HNLDEPFJ_00186 | 7e-110 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
HNLDEPFJ_00187 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
HNLDEPFJ_00188 | 3.3e-118 | 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 | |
HNLDEPFJ_00189 | 1.3e-287 | ahpF | O | alkyl hydroperoxide reductase | ||
HNLDEPFJ_00190 | 2.4e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
HNLDEPFJ_00191 | 8.2e-123 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
HNLDEPFJ_00192 | 7.9e-230 | L | Transposase | |||
HNLDEPFJ_00193 | 1.4e-256 | rnjA | S | 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 | ||
HNLDEPFJ_00194 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
HNLDEPFJ_00195 | 3.5e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
HNLDEPFJ_00196 | 1.1e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
HNLDEPFJ_00197 | 1.6e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
HNLDEPFJ_00198 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
HNLDEPFJ_00199 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
HNLDEPFJ_00200 | 6.3e-131 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
HNLDEPFJ_00201 | 3.6e-168 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
HNLDEPFJ_00202 | 2.4e-119 | 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 | |
HNLDEPFJ_00203 | 5.5e-301 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
HNLDEPFJ_00204 | 6.6e-81 | smpB | O | 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 | ||
HNLDEPFJ_00205 | 7.1e-175 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
HNLDEPFJ_00206 | 1.7e-143 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
HNLDEPFJ_00207 | 2.2e-43 | comGC | U | Required for transformation and DNA binding | ||
HNLDEPFJ_00208 | 2.4e-69 | cglD | NU | Competence protein | ||
HNLDEPFJ_00209 | 5.3e-15 | NU | Type II secretory pathway pseudopilin | |||
HNLDEPFJ_00212 | 2e-89 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
HNLDEPFJ_00213 | 1.8e-223 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
HNLDEPFJ_00214 | 1.8e-61 | yutD | J | protein conserved in bacteria | ||
HNLDEPFJ_00215 | 8.7e-85 | 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 | ||
HNLDEPFJ_00216 | 1.6e-77 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
HNLDEPFJ_00217 | 4e-122 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
HNLDEPFJ_00218 | 2.4e-16 | 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 | ||
HNLDEPFJ_00220 | 5.8e-163 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
HNLDEPFJ_00222 | 3.9e-96 | ywlG | S | Belongs to the UPF0340 family | ||
HNLDEPFJ_00224 | 3.4e-72 | S | QueT transporter | |||
HNLDEPFJ_00225 | 5.3e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
HNLDEPFJ_00226 | 1.1e-242 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
HNLDEPFJ_00227 | 1.8e-90 | K | transcriptional regulator | |||
HNLDEPFJ_00228 | 1.6e-36 | yneF | S | UPF0154 protein | ||
HNLDEPFJ_00229 | 7.9e-154 | fhuR | K | transcriptional regulator (lysR family) | ||
HNLDEPFJ_00230 | 4.4e-77 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
HNLDEPFJ_00231 | 9.4e-161 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
HNLDEPFJ_00232 | 4.8e-88 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
HNLDEPFJ_00234 | 8.7e-140 | ykuT | M | mechanosensitive ion channel | ||
HNLDEPFJ_00235 | 3.9e-87 | sigH | K | DNA-templated transcription, initiation | ||
HNLDEPFJ_00236 | 1.2e-135 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
HNLDEPFJ_00237 | 3e-114 | papP | P | ABC transporter (Permease | ||
HNLDEPFJ_00238 | 4.6e-107 | P | ABC transporter (Permease | |||
HNLDEPFJ_00239 | 5.3e-254 | yfmR | S | abc transporter atp-binding protein | ||
HNLDEPFJ_00240 | 1.3e-26 | U | response to pH | |||
HNLDEPFJ_00241 | 3.5e-118 | 3.6.1.13, 3.6.1.55 | F | AdP-ribose pyrophosphatase | ||
HNLDEPFJ_00242 | 8.7e-139 | 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 | |
HNLDEPFJ_00243 | 1.4e-245 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
HNLDEPFJ_00244 | 5.9e-202 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
HNLDEPFJ_00245 | 6.4e-218 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
HNLDEPFJ_00246 | 1.9e-96 | yloV | S | kinase related to dihydroxyacetone kinase | ||
HNLDEPFJ_00247 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HNLDEPFJ_00248 | 3.1e-26 | dmpI | 5.3.2.6 | G | Tautomerase enzyme | |
HNLDEPFJ_00249 | 2e-107 | S | Putative adhesin | |||
HNLDEPFJ_00250 | 5.4e-110 | XK27_06930 | V | domain protein | ||
HNLDEPFJ_00251 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HNLDEPFJ_00252 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
HNLDEPFJ_00253 | 1.4e-31 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
HNLDEPFJ_00254 | 1.6e-61 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
HNLDEPFJ_00255 | 2.4e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNLDEPFJ_00256 | 4.4e-62 | rplQ | J | ribosomal protein l17 | ||
HNLDEPFJ_00257 | 8e-61 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNLDEPFJ_00258 | 1.4e-158 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
HNLDEPFJ_00259 | 1.6e-252 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
HNLDEPFJ_00260 | 1.6e-123 | sip | M | LysM domain protein | ||
HNLDEPFJ_00261 | 3.7e-34 | yozE | S | Belongs to the UPF0346 family | ||
HNLDEPFJ_00262 | 7.3e-29 | cvfB | S | Protein conserved in bacteria | ||
HNLDEPFJ_00263 | 7.9e-70 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
HNLDEPFJ_00264 | 1.4e-173 | 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 | |
HNLDEPFJ_00265 | 9.3e-211 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
HNLDEPFJ_00266 | 1.3e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
HNLDEPFJ_00267 | 1.5e-26 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
HNLDEPFJ_00268 | 6e-186 | ylbL | T | Belongs to the peptidase S16 family | ||
HNLDEPFJ_00269 | 5.4e-183 | yhcC | S | radical SAM protein | ||
HNLDEPFJ_00270 | 5.8e-247 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
HNLDEPFJ_00271 | 4.7e-58 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
HNLDEPFJ_00272 | 1e-84 | endA | F | DNA RNA non-specific endonuclease | ||
HNLDEPFJ_00273 | 2.9e-111 | tcyB_2 | P | ABC transporter (permease) | ||
HNLDEPFJ_00274 | 1.9e-116 | gltJ | P | ABC transporter (Permease | ||
HNLDEPFJ_00275 | 3e-105 | peb1A | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
HNLDEPFJ_00277 | 3.9e-99 | thiT | S | Thiamine transporter | ||
HNLDEPFJ_00278 | 1.2e-238 | 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 | ||
HNLDEPFJ_00279 | 0.0 | scrA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNLDEPFJ_00280 | 7.3e-115 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HNLDEPFJ_00281 | 5e-54 | S | HAD hydrolase, family IA, variant | |||
HNLDEPFJ_00282 | 5.3e-58 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
HNLDEPFJ_00283 | 1.1e-219 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
HNLDEPFJ_00284 | 1.5e-225 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
HNLDEPFJ_00285 | 0.0 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
HNLDEPFJ_00286 | 2.5e-203 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
HNLDEPFJ_00287 | 1.1e-189 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
HNLDEPFJ_00288 | 1.2e-218 | metE | 2.1.1.14 | E | Methionine synthase | |
HNLDEPFJ_00289 | 1.5e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
HNLDEPFJ_00290 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
HNLDEPFJ_00291 | 3e-145 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
HNLDEPFJ_00292 | 1.6e-49 | |||||
HNLDEPFJ_00293 | 1.7e-32 | |||||
HNLDEPFJ_00294 | 5.3e-73 | |||||
HNLDEPFJ_00295 | 2.3e-240 | O | MreB/Mbl protein | |||
HNLDEPFJ_00297 | 5.3e-265 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
HNLDEPFJ_00298 | 3.9e-136 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNLDEPFJ_00299 | 1.9e-176 | ecsB | U | Bacterial ABC transporter protein EcsB | ||
HNLDEPFJ_00300 | 4.4e-140 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
HNLDEPFJ_00301 | 1.5e-29 | K | Helix-turn-helix domain | |||
HNLDEPFJ_00302 | 1.2e-18 | |||||
HNLDEPFJ_00303 | 1.2e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
HNLDEPFJ_00304 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
HNLDEPFJ_00305 | 5.1e-22 | K | Transcriptional | |||
HNLDEPFJ_00306 | 6.3e-108 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
HNLDEPFJ_00307 | 4e-75 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
HNLDEPFJ_00308 | 1.1e-75 | 3.5.1.19 | Q | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | ||
HNLDEPFJ_00309 | 0.0 | V | ABC transporter (Permease | |||
HNLDEPFJ_00310 | 7.7e-118 | 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 | |
HNLDEPFJ_00311 | 2e-26 | |||||
HNLDEPFJ_00312 | 7.7e-97 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
HNLDEPFJ_00313 | 3.6e-60 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
HNLDEPFJ_00314 | 3e-38 | ptsH | G | phosphocarrier protein Hpr | ||
HNLDEPFJ_00315 | 1.6e-297 | V | abc transporter atp-binding protein | |||
HNLDEPFJ_00316 | 3.9e-98 | XK27_09740 | S | Phosphoesterase | ||
HNLDEPFJ_00317 | 1.7e-184 | 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 | |
HNLDEPFJ_00318 | 1.1e-113 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
HNLDEPFJ_00319 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
HNLDEPFJ_00320 | 2.4e-195 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
HNLDEPFJ_00321 | 3.9e-139 | V | ABC-type multidrug transport system ATPase and permease | |||
HNLDEPFJ_00322 | 5.7e-127 | 3.5.1.28 | M | domain protein | ||
HNLDEPFJ_00323 | 2.7e-89 | maa | 2.3.1.79 | GK | Maltose O-acetyltransferase | |
HNLDEPFJ_00324 | 6.2e-67 | rmaI | K | Transcriptional regulator, MarR family | ||
HNLDEPFJ_00325 | 2.8e-93 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
HNLDEPFJ_00326 | 2.3e-50 | nadK | 2.7.1.23 | H | 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 | |
HNLDEPFJ_00327 | 6e-91 | nadK | 2.7.1.23 | H | 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 | |
HNLDEPFJ_00328 | 8.8e-119 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
HNLDEPFJ_00329 | 1.7e-69 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
HNLDEPFJ_00330 | 9.7e-36 | XK27_09805 | S | MORN repeat protein | ||
HNLDEPFJ_00331 | 1.5e-55 | S | Psort location Cytoplasmic, score 8.87 | |||
HNLDEPFJ_00332 | 2.6e-87 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
HNLDEPFJ_00333 | 7.1e-217 | ydaO | E | amino acid | ||
HNLDEPFJ_00334 | 1.3e-294 | copA | 3.6.3.54 | P | P-type ATPase | |
HNLDEPFJ_00335 | 2.7e-31 | copZ | 2.7.7.77 | P | Heavy metal-associated domain protein | |
HNLDEPFJ_00336 | 2.6e-123 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
HNLDEPFJ_00337 | 6e-149 | corA | P | COG0598 Mg2 and Co2 transporters | ||
HNLDEPFJ_00338 | 3.3e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
HNLDEPFJ_00339 | 1.8e-187 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
HNLDEPFJ_00340 | 5.6e-124 | |||||
HNLDEPFJ_00341 | 7.5e-21 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
HNLDEPFJ_00342 | 2.3e-267 | pepD | E | Dipeptidase | ||
HNLDEPFJ_00343 | 4.1e-110 | XK27_10720 | D | peptidase activity | ||
HNLDEPFJ_00344 | 6.6e-122 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
HNLDEPFJ_00345 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
HNLDEPFJ_00346 | 1.2e-141 | cmpC | S | abc transporter atp-binding protein | ||
HNLDEPFJ_00347 | 2.3e-132 | WQ51_06230 | S | ABC transporter | ||
HNLDEPFJ_00348 | 2.9e-151 | degV | S | DegV family | ||
HNLDEPFJ_00349 | 1.2e-82 | yacP | S | RNA-binding protein containing a PIN domain | ||
HNLDEPFJ_00350 | 1.1e-22 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
HNLDEPFJ_00351 | 1.4e-62 | S | MORN repeat variant | |||
HNLDEPFJ_00353 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
HNLDEPFJ_00354 | 6.1e-205 | 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 | ||
HNLDEPFJ_00355 | 2.3e-54 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
HNLDEPFJ_00356 | 1.9e-53 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
HNLDEPFJ_00357 | 1.7e-243 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
HNLDEPFJ_00358 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
HNLDEPFJ_00359 | 3.6e-45 | speD | 2.5.1.16, 4.1.1.50 | H | Catalyzes the decarboxylation of S-adenosylmethionine to S-adenosylmethioninamine (dcAdoMet), the propylamine donor required for the synthesis of the polyamines spermine and spermidine from the diamine putrescine | |
HNLDEPFJ_00362 | 4.8e-143 | 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 | ||
HNLDEPFJ_00363 | 5.1e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
HNLDEPFJ_00364 | 5.8e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
HNLDEPFJ_00365 | 1.3e-68 | lysA | 4.1.1.20 | E | Psort location Cytoplasmic, score 8.87 | |
HNLDEPFJ_00366 | 4.9e-164 | EGP | Major facilitator Superfamily | |||
HNLDEPFJ_00367 | 1.8e-72 | copY | K | negative regulation of transcription, DNA-templated | ||
HNLDEPFJ_00368 | 9.2e-116 | 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 | ||
HNLDEPFJ_00369 | 8.6e-57 | 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 | ||
HNLDEPFJ_00370 | 1e-99 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
HNLDEPFJ_00371 | 5.1e-15 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
HNLDEPFJ_00372 | 5.7e-252 | glnA | 6.3.1.2 | E | glutamine synthetase | |
HNLDEPFJ_00373 | 8.8e-27 | lanR | K | sequence-specific DNA binding | ||
HNLDEPFJ_00374 | 2.9e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
HNLDEPFJ_00375 | 2.4e-49 | L | COG1943 Transposase and inactivated derivatives | |||
HNLDEPFJ_00376 | 3.6e-31 | L | Integrase core domain protein | |||
HNLDEPFJ_00377 | 1.3e-114 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
HNLDEPFJ_00378 | 2e-71 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
HNLDEPFJ_00379 | 7.3e-234 | 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 | ||
HNLDEPFJ_00380 | 3.9e-215 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HNLDEPFJ_00381 | 2.8e-24 | secE | U | Belongs to the SecE SEC61-gamma family | ||
HNLDEPFJ_00382 | 1.6e-109 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
HNLDEPFJ_00383 | 1e-104 | wecD | M | Acetyltransferase (GNAT) domain | ||
HNLDEPFJ_00384 | 3.5e-137 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
HNLDEPFJ_00385 | 1.3e-105 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
HNLDEPFJ_00386 | 8.4e-17 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
HNLDEPFJ_00387 | 2e-158 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
HNLDEPFJ_00388 | 4e-84 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
HNLDEPFJ_00389 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
HNLDEPFJ_00390 | 9.2e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
HNLDEPFJ_00391 | 7.7e-166 | 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 | ||
HNLDEPFJ_00392 | 9.6e-261 | 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 | |
HNLDEPFJ_00393 | 9.4e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HNLDEPFJ_00394 | 9.9e-73 | sufB | O | assembly protein SufB | ||
HNLDEPFJ_00395 | 7.7e-92 | lemA | S | LemA family | ||
HNLDEPFJ_00396 | 9.1e-16 | 2.4.1.21 | GT5 | M | Right handed beta helix region | |
HNLDEPFJ_00398 | 3.5e-56 | lrgA | S | Effector of murein hydrolase LrgA | ||
HNLDEPFJ_00399 | 3.2e-116 | lrgB | M | Inhibits the expression or activity of extracellular murein hydrolases by interacting, possibly with LrgA, with the holin-like proteins CidA and or CidB. The LrgAB and CidAB proteins may affect the proton motive force of the membrane. May be involved in programmed cell death (PCD), possibly triggering PCD in response to antibiotics and environmental stresses | ||
HNLDEPFJ_00400 | 2.1e-140 | fnt | P | Formate nitrite transporter | ||
HNLDEPFJ_00401 | 1.8e-96 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
HNLDEPFJ_00402 | 2.5e-56 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
HNLDEPFJ_00403 | 3.1e-69 | argR | K | Regulates arginine biosynthesis genes | ||
HNLDEPFJ_00404 | 5.9e-105 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
HNLDEPFJ_00405 | 3.1e-145 | G | Domain of Unknown Function (DUF1080) | |||
HNLDEPFJ_00406 | 1.9e-98 | U | protein secretion | |||
HNLDEPFJ_00407 | 3.2e-192 | zmpB | M | signal peptide protein, YSIRK family | ||
HNLDEPFJ_00408 | 6.7e-80 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
HNLDEPFJ_00409 | 5.2e-303 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
HNLDEPFJ_00410 | 1.6e-152 | corA | P | CorA-like protein | ||
HNLDEPFJ_00411 | 3.7e-149 | rarD | S | Transporter | ||
HNLDEPFJ_00412 | 9.8e-16 | T | peptidase | |||
HNLDEPFJ_00413 | 4.6e-183 | amt | P | Ammonium Transporter | ||
HNLDEPFJ_00414 | 3.1e-34 | amt | P | Ammonium Transporter | ||
HNLDEPFJ_00415 | 1.1e-53 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
HNLDEPFJ_00416 | 3.6e-73 | yccU | S | CoA-binding protein | ||
HNLDEPFJ_00417 | 2.4e-50 | trxA | O | Belongs to the thioredoxin family | ||
HNLDEPFJ_00418 | 6e-143 | S | Macro domain protein | |||
HNLDEPFJ_00419 | 9.3e-79 | treB | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
HNLDEPFJ_00420 | 3.4e-28 | 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 | |
HNLDEPFJ_00421 | 6.6e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
HNLDEPFJ_00422 | 2.3e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
HNLDEPFJ_00423 | 2.5e-81 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
HNLDEPFJ_00424 | 1.7e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
HNLDEPFJ_00425 | 6.3e-213 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
HNLDEPFJ_00426 | 1.7e-163 | fruA | 2.7.1.202 | G | phosphotransferase system | |
HNLDEPFJ_00427 | 9.6e-74 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
HNLDEPFJ_00428 | 6e-269 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
HNLDEPFJ_00429 | 7.1e-153 | yvjA | S | membrane | ||
HNLDEPFJ_00430 | 5.6e-155 | rrmA | 2.1.1.187 | Q | methyltransferase | |
HNLDEPFJ_00431 | 4.2e-69 | ytxH | S | General stress protein | ||
HNLDEPFJ_00432 | 3.7e-08 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
HNLDEPFJ_00433 | 8e-108 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
HNLDEPFJ_00434 | 2.5e-34 | ylmH | S | conserved protein, contains S4-like domain | ||
HNLDEPFJ_00435 | 8.4e-138 | divIVA | D | Cell division initiation protein | ||
HNLDEPFJ_00436 | 1.9e-88 | L | COG1943 Transposase and inactivated derivatives | |||
HNLDEPFJ_00437 | 1.2e-64 | tsaD | 2.3.1.234 | O | 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 | |
HNLDEPFJ_00438 | 1.8e-114 | azlC | E | AzlC protein | ||
HNLDEPFJ_00439 | 4.8e-46 | azlD | S | branched-chain amino acid | ||
HNLDEPFJ_00440 | 4.2e-156 | 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 | ||
HNLDEPFJ_00441 | 1.9e-110 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
HNLDEPFJ_00442 | 1.8e-90 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
HNLDEPFJ_00443 | 1.2e-211 | 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 | ||
HNLDEPFJ_00444 | 7e-218 | pyrP | F | uracil Permease | ||
HNLDEPFJ_00446 | 8.6e-171 | yfjR | K | regulation of single-species biofilm formation | ||
HNLDEPFJ_00447 | 4e-284 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
HNLDEPFJ_00448 | 7.3e-74 | L | Transposase IS116/IS110/IS902 family | |||
HNLDEPFJ_00449 | 1.1e-155 | S | CHAP domain | |||
HNLDEPFJ_00450 | 1.9e-170 | vraS | 2.7.13.3 | T | Histidine kinase | |
HNLDEPFJ_00451 | 1.5e-83 | yvqF | S | Membrane | ||
HNLDEPFJ_00452 | 3.6e-85 | pelG | M | Putative exopolysaccharide Exporter (EPS-E) | ||
HNLDEPFJ_00453 | 4.1e-83 | 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 | |
HNLDEPFJ_00454 | 1.3e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
HNLDEPFJ_00455 | 1.1e-119 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
HNLDEPFJ_00456 | 7.6e-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 | ||
HNLDEPFJ_00457 | 1.9e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
HNLDEPFJ_00458 | 5.1e-57 | yhcA | V | abc transporter atp-binding protein | ||
HNLDEPFJ_00459 | 1e-37 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
HNLDEPFJ_00460 | 1e-80 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
HNLDEPFJ_00461 | 9.8e-28 | 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 | ||
HNLDEPFJ_00462 | 2.4e-63 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
HNLDEPFJ_00463 | 4.5e-52 | U | protein secretion | |||
HNLDEPFJ_00464 | 5.9e-109 | yvyE | 3.4.13.9 | S | YigZ family | |
HNLDEPFJ_00465 | 2.8e-246 | L | Reverse transcriptase (RNA-dependent DNA polymerase) | |||
HNLDEPFJ_00466 | 6.4e-265 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
HNLDEPFJ_00467 | 5.1e-165 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination | |
HNLDEPFJ_00468 | 3.7e-160 | dcuS | 2.7.13.3 | T | protein histidine kinase activity | |
HNLDEPFJ_00469 | 1.1e-223 | 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) | |
HNLDEPFJ_00470 | 2.9e-158 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
HNLDEPFJ_00471 | 3.9e-81 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
HNLDEPFJ_00472 | 1.5e-89 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
HNLDEPFJ_00473 | 3.9e-114 | S | VIT family | |||
HNLDEPFJ_00474 | 8.2e-97 | 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 | |
HNLDEPFJ_00475 | 1.5e-96 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18 | GH23 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
HNLDEPFJ_00476 | 3.1e-77 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
HNLDEPFJ_00479 | 3.5e-154 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
HNLDEPFJ_00480 | 2.2e-199 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
HNLDEPFJ_00481 | 2.3e-142 | 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 | |
HNLDEPFJ_00482 | 4.2e-141 | L | PFAM transposase IS116 IS110 IS902 family | |||
HNLDEPFJ_00483 | 7.2e-65 | L | Transposase (IS116 IS110 IS902 family) | |||
HNLDEPFJ_00484 | 1.7e-116 | S | double-stranded DNA endodeoxyribonuclease activity | |||
HNLDEPFJ_00485 | 2e-236 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
HNLDEPFJ_00486 | 1.5e-104 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HNLDEPFJ_00489 | 9e-181 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
HNLDEPFJ_00490 | 3.2e-144 | 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 | ||
HNLDEPFJ_00491 | 2.8e-88 | malF | P | ABC transporter (Permease | ||
HNLDEPFJ_00492 | 5.4e-76 | malG | P | ABC transporter (Permease | ||
HNLDEPFJ_00493 | 1.5e-52 | malG | P | ABC transporter (Permease | ||
HNLDEPFJ_00494 | 2.5e-239 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
HNLDEPFJ_00495 | 1.5e-194 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
HNLDEPFJ_00496 | 6.1e-154 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
HNLDEPFJ_00497 | 5.7e-92 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
HNLDEPFJ_00498 | 6.4e-37 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
HNLDEPFJ_00499 | 1.3e-144 | |||||
HNLDEPFJ_00500 | 2e-98 | XK27_00765 | ||||
HNLDEPFJ_00501 | 5.8e-109 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
HNLDEPFJ_00502 | 5.1e-46 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
HNLDEPFJ_00503 | 2.4e-176 | 3.6.3.8 | P | cation transport ATPase | ||
HNLDEPFJ_00504 | 5.5e-196 | 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) | |
HNLDEPFJ_00505 | 6.1e-93 | XK27_05000 | S | metal cluster binding | ||
HNLDEPFJ_00506 | 2.2e-29 | liaI | KT | membrane | ||
HNLDEPFJ_00507 | 9e-16 | S | dextransucrase activity | |||
HNLDEPFJ_00508 | 1.2e-50 | S | Protein of unknown function (DUF3397) | |||
HNLDEPFJ_00509 | 9.2e-89 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
HNLDEPFJ_00510 | 8.6e-23 | 2.7.13.3 | T | GHKL domain | ||
HNLDEPFJ_00511 | 1.3e-116 | yyaQ | S | YjbR | ||
HNLDEPFJ_00512 | 6e-73 | cbiQ | P | cobalt transport | ||
HNLDEPFJ_00513 | 9.4e-121 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
HNLDEPFJ_00514 | 6.6e-193 | 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) | ||
HNLDEPFJ_00515 | 1.5e-117 | nudL | L | hydrolase | ||
HNLDEPFJ_00516 | 6.3e-54 | K | transcriptional regulator, PadR family | |||
HNLDEPFJ_00517 | 4.9e-174 | manL | 2.7.1.191 | G | pts system | |
HNLDEPFJ_00518 | 4.4e-71 | S | abc transporter atp-binding protein | |||
HNLDEPFJ_00519 | 6.2e-48 | yxjI | S | LURP-one-related | ||
HNLDEPFJ_00520 | 2.4e-93 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
HNLDEPFJ_00523 | 4.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
HNLDEPFJ_00524 | 1.4e-187 | tcsA | S | membrane | ||
HNLDEPFJ_00525 | 3.5e-213 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
HNLDEPFJ_00526 | 1.6e-227 | pacL | 3.6.3.8 | P | cation transport ATPase | |
HNLDEPFJ_00527 | 2.4e-106 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HNLDEPFJ_00528 | 3.7e-116 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
HNLDEPFJ_00529 | 3.2e-209 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
HNLDEPFJ_00530 | 1.2e-117 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HNLDEPFJ_00531 | 2.9e-48 | yhbY | J | RNA-binding protein | ||
HNLDEPFJ_00532 | 2.3e-22 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNLDEPFJ_00533 | 1.3e-117 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
HNLDEPFJ_00534 | 3.6e-16 | S | Accessory secretory protein Sec, Asp5 | |||
HNLDEPFJ_00535 | 5.9e-155 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HNLDEPFJ_00536 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
HNLDEPFJ_00537 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
HNLDEPFJ_00538 | 2.1e-135 | cycA | E | permease | ||
HNLDEPFJ_00539 | 5e-40 | K | Acetyltransferase (GNAT) family | |||
HNLDEPFJ_00540 | 7.4e-112 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
HNLDEPFJ_00541 | 4.7e-143 | G | COG0457 FOG TPR repeat | |||
HNLDEPFJ_00543 | 4.2e-156 | XK27_03015 | S | permease | ||
HNLDEPFJ_00544 | 9.4e-77 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
HNLDEPFJ_00545 | 8.7e-90 | XK27_05885 | 2.3.1.82 | M | phosphinothricin N-acetyltransferase activity | |
HNLDEPFJ_00546 | 4.3e-33 | ykuJ | S | protein conserved in bacteria | ||
HNLDEPFJ_00547 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
HNLDEPFJ_00548 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
HNLDEPFJ_00549 | 2.3e-35 | vgrG | S | Rhs Element Vgr Protein | ||
HNLDEPFJ_00550 | 2.7e-106 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
HNLDEPFJ_00551 | 3e-215 | L | Transposase | |||
HNLDEPFJ_00552 | 4.5e-76 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
HNLDEPFJ_00553 | 2e-100 | pncA | Q | isochorismatase | ||
HNLDEPFJ_00554 | 4.4e-80 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
HNLDEPFJ_00555 | 9e-197 | yceA | S | Belongs to the UPF0176 family | ||
HNLDEPFJ_00556 | 7.9e-39 | ccl | S | cog cog4708 | ||
HNLDEPFJ_00557 | 6e-105 | nodB3 | G | deacetylase | ||
HNLDEPFJ_00558 | 3.2e-104 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
HNLDEPFJ_00559 | 5.1e-41 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
HNLDEPFJ_00560 | 3.5e-157 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
HNLDEPFJ_00561 | 1.1e-169 | 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 | |
HNLDEPFJ_00562 | 1.1e-195 | ylbM | S | Belongs to the UPF0348 family | ||
HNLDEPFJ_00563 | 7.1e-33 | S | RloB-like protein | |||
HNLDEPFJ_00564 | 7.5e-39 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
HNLDEPFJ_00565 | 3.8e-23 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
HNLDEPFJ_00566 | 3.3e-11 | divIC | D | Septum formation initiator | ||
HNLDEPFJ_00567 | 1.9e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
HNLDEPFJ_00568 | 8.7e-41 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
HNLDEPFJ_00572 | 5.3e-184 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
HNLDEPFJ_00573 | 2e-101 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
HNLDEPFJ_00574 | 1e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
HNLDEPFJ_00576 | 8.3e-54 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
HNLDEPFJ_00577 | 2.7e-111 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
HNLDEPFJ_00578 | 1.1e-40 | pspC | KT | PspC domain | ||
HNLDEPFJ_00579 | 6.8e-16 | pspC | KT | PspC domain protein | ||
HNLDEPFJ_00580 | 5.2e-119 | yqfA | K | protein, Hemolysin III | ||
HNLDEPFJ_00581 | 2.1e-166 | yjcE | P | NhaP-type Na H and K H antiporters | ||
HNLDEPFJ_00582 | 1.9e-07 | |||||
HNLDEPFJ_00583 | 2.5e-95 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HNLDEPFJ_00584 | 6.5e-134 | GK | ROK family | |||
HNLDEPFJ_00585 | 2.8e-79 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
HNLDEPFJ_00586 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
HNLDEPFJ_00587 | 7.1e-167 | dnaB | L | Replication initiation and membrane attachment | ||
HNLDEPFJ_00588 | 9e-72 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
HNLDEPFJ_00589 | 6.4e-176 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
HNLDEPFJ_00590 | 4.6e-88 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
HNLDEPFJ_00591 | 1.5e-172 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
HNLDEPFJ_00592 | 9.7e-22 | |||||
HNLDEPFJ_00593 | 8.4e-78 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
HNLDEPFJ_00594 | 1e-66 | DegV | S | DegV family | ||
HNLDEPFJ_00595 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
HNLDEPFJ_00596 | 7.8e-45 | 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 | |
HNLDEPFJ_00598 | 1.2e-39 | era | M | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HNLDEPFJ_00599 | 2e-107 | era | M | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
HNLDEPFJ_00600 | 3.6e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HNLDEPFJ_00601 | 8.7e-34 | T | PhoQ Sensor | |||
HNLDEPFJ_00602 | 6.1e-82 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
HNLDEPFJ_00603 | 1.5e-36 | ylqC | L | Belongs to the UPF0109 family | ||
HNLDEPFJ_00604 | 1.5e-138 | 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) | |
HNLDEPFJ_00605 | 1.1e-33 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HNLDEPFJ_00606 | 8.3e-37 | mtsC | P | ABC-type Mn2 Zn2 transport systems, permease components | ||
HNLDEPFJ_00607 | 4.6e-177 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
HNLDEPFJ_00608 | 9.1e-158 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
HNLDEPFJ_00609 | 1.4e-160 | S | dextransucrase activity | |||
HNLDEPFJ_00610 | 3.7e-120 | 2.7.7.7 | L | the current gene model (or a revised gene model) may contain a frame shift | ||
HNLDEPFJ_00612 | 9.1e-175 | potD | P | spermidine putrescine ABC transporter | ||
HNLDEPFJ_00613 | 8.3e-75 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
HNLDEPFJ_00614 | 2.6e-140 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
HNLDEPFJ_00615 | 1.2e-132 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
HNLDEPFJ_00616 | 3.8e-198 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
HNLDEPFJ_00617 | 1.1e-37 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
HNLDEPFJ_00618 | 1.5e-64 | pheS | 6.1.1.20 | J | Aminoacyl tRNA synthetase class II, N-terminal domain | |
HNLDEPFJ_00619 | 1.9e-37 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
HNLDEPFJ_00620 | 1.5e-45 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
HNLDEPFJ_00621 | 1.1e-167 | XK27_09615 | C | reductase | ||
HNLDEPFJ_00622 | 8.9e-153 | yitS | S | EDD domain protein, DegV family | ||
HNLDEPFJ_00623 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
HNLDEPFJ_00624 | 8.7e-13 | |||||
HNLDEPFJ_00625 | 3e-133 | S | hydrolase | |||
HNLDEPFJ_00626 | 5.6e-19 | fruA | 2.7.1.202 | G | phosphotransferase system | |
HNLDEPFJ_00627 | 4.8e-99 | 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 | |
HNLDEPFJ_00628 | 2.1e-13 | rplD | J | Forms part of the polypeptide exit tunnel | ||
HNLDEPFJ_00629 | 9.2e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
HNLDEPFJ_00630 | 6.8e-116 | K | Response regulator receiver domain protein | |||
HNLDEPFJ_00631 | 5.3e-189 | yegQ | O | Peptidase U32 | ||
HNLDEPFJ_00632 | 4.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
HNLDEPFJ_00633 | 8.7e-198 | 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 | ||
HNLDEPFJ_00634 | 9.6e-142 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
HNLDEPFJ_00635 | 7e-28 | M | Putative cell wall binding repeat | |||
HNLDEPFJ_00636 | 2.6e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
HNLDEPFJ_00637 | 7.5e-89 | S | unusual protein kinase | |||
HNLDEPFJ_00638 | 1.8e-133 | 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 | |
HNLDEPFJ_00639 | 6.4e-38 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
HNLDEPFJ_00642 | 2.2e-27 | XK27_05745 | ||||
HNLDEPFJ_00643 | 1.4e-84 | E | Alpha beta hydrolase | |||
HNLDEPFJ_00644 | 7e-71 | yaeR | E | COG0346 Lactoylglutathione lyase and related lyases | ||
HNLDEPFJ_00645 | 3e-84 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
HNLDEPFJ_00646 | 5.7e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
HNLDEPFJ_00647 | 2.7e-91 | niaR | S | small molecule binding protein (contains 3H domain) | ||
HNLDEPFJ_00648 | 3.6e-111 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
HNLDEPFJ_00649 | 2e-143 | oppD | P | Belongs to the ABC transporter superfamily | ||
HNLDEPFJ_00650 | 5.8e-141 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
HNLDEPFJ_00651 | 2.6e-97 | dltB | M | Membrane protein involved in D-alanine export | ||
HNLDEPFJ_00652 | 2.2e-35 | dltC | 6.1.1.13 | IQ | 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 | |
HNLDEPFJ_00653 | 5.8e-55 | mprF | 2.3.2.3 | J | 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 | |
HNLDEPFJ_00654 | 1.4e-63 | XK27_00115 | 2.3.1.128 | K | Acetyltransferase GNAT family | |
HNLDEPFJ_00655 | 7.7e-67 | ywiB | S | Domain of unknown function (DUF1934) | ||
HNLDEPFJ_00656 | 4.4e-132 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
HNLDEPFJ_00657 | 1.9e-90 | 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 | ||
HNLDEPFJ_00658 | 3.3e-71 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
HNLDEPFJ_00659 | 3.7e-108 | yeaB | K | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
HNLDEPFJ_00660 | 2.7e-62 | norN | V | Mate efflux family protein | ||
HNLDEPFJ_00661 | 9.5e-38 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
HNLDEPFJ_00662 | 1.7e-75 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HNLDEPFJ_00663 | 3.1e-157 | 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 | ||
HNLDEPFJ_00664 | 2.6e-75 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
HNLDEPFJ_00665 | 1.3e-39 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
HNLDEPFJ_00666 | 3.1e-101 | M | domain protein | |||
HNLDEPFJ_00667 | 9.1e-42 | WQ51_02910 | S | Protein of unknown function, DUF536 | ||
HNLDEPFJ_00668 | 1.2e-43 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
HNLDEPFJ_00670 | 2.8e-18 | 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 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)