ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
NPJHOEFD_00001 | 1.6e-43 | S | aldo-keto reductase (NADP) activity | |||
NPJHOEFD_00002 | 6.2e-96 | sip | L | Belongs to the 'phage' integrase family | ||
NPJHOEFD_00005 | 1.6e-15 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_00006 | 6.6e-11 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_00009 | 1.2e-09 | |||||
NPJHOEFD_00010 | 7.5e-08 | K | DNA-binding helix-turn-helix protein | |||
NPJHOEFD_00014 | 8.9e-55 | S | Protein of unknown function (DUF1351) | |||
NPJHOEFD_00015 | 4.9e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
NPJHOEFD_00016 | 1.8e-200 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
NPJHOEFD_00017 | 4.2e-92 | S | SNARE associated Golgi protein | |||
NPJHOEFD_00018 | 2.9e-156 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
NPJHOEFD_00019 | 1.4e-159 | 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) | |
NPJHOEFD_00020 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
NPJHOEFD_00021 | 2.8e-102 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
NPJHOEFD_00022 | 6.7e-37 | |||||
NPJHOEFD_00023 | 3.7e-90 | gluC | P | ABC transporter permease | ||
NPJHOEFD_00024 | 1.2e-146 | glnH | ET | ABC transporter substrate-binding protein | ||
NPJHOEFD_00025 | 4.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NPJHOEFD_00026 | 3.8e-46 | udk | 2.7.1.48 | F | Zeta toxin | |
NPJHOEFD_00027 | 9.8e-39 | udk | 2.7.1.48 | F | Zeta toxin | |
NPJHOEFD_00028 | 1e-246 | G | MFS/sugar transport protein | |||
NPJHOEFD_00029 | 1.6e-100 | S | ABC-type cobalt transport system, permease component | |||
NPJHOEFD_00030 | 7.3e-112 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NPJHOEFD_00031 | 1.3e-125 | gntR1 | K | UTRA | ||
NPJHOEFD_00032 | 5.1e-71 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
NPJHOEFD_00033 | 2.1e-134 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
NPJHOEFD_00034 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
NPJHOEFD_00035 | 2e-157 | S | reductase | |||
NPJHOEFD_00036 | 9.3e-35 | |||||
NPJHOEFD_00037 | 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 | |
NPJHOEFD_00038 | 6e-76 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
NPJHOEFD_00039 | 3.5e-142 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
NPJHOEFD_00040 | 6.6e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
NPJHOEFD_00041 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NPJHOEFD_00042 | 2.6e-208 | frdC | 1.3.5.4 | C | FAD binding domain | |
NPJHOEFD_00043 | 2e-178 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
NPJHOEFD_00045 | 1.8e-24 | srtA | 3.4.22.70 | M | sortase family | |
NPJHOEFD_00046 | 3e-270 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
NPJHOEFD_00047 | 1e-24 | |||||
NPJHOEFD_00048 | 9.5e-26 | |||||
NPJHOEFD_00049 | 2.5e-33 | |||||
NPJHOEFD_00050 | 1.4e-53 | S | Enterocin A Immunity | |||
NPJHOEFD_00051 | 8e-145 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
NPJHOEFD_00052 | 5.5e-305 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
NPJHOEFD_00053 | 7.7e-191 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
NPJHOEFD_00054 | 1.4e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
NPJHOEFD_00055 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
NPJHOEFD_00056 | 5.9e-117 | L | COG2826 Transposase and inactivated derivatives, IS30 family | |||
NPJHOEFD_00057 | 4.7e-88 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
NPJHOEFD_00058 | 8.3e-106 | S | Repeat protein | |||
NPJHOEFD_00059 | 1.6e-108 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
NPJHOEFD_00060 | 5.1e-220 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
NPJHOEFD_00061 | 5.4e-56 | XK27_04120 | S | Putative amino acid metabolism | ||
NPJHOEFD_00062 | 1.5e-144 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
NPJHOEFD_00064 | 4.1e-09 | S | Arc-like DNA binding domain | |||
NPJHOEFD_00066 | 1.3e-30 | K | Helix-turn-helix domain | |||
NPJHOEFD_00067 | 1.3e-20 | XK27_07105 | K | Helix-turn-helix XRE-family like proteins | ||
NPJHOEFD_00068 | 3.9e-15 | K | Cro/C1-type HTH DNA-binding domain | |||
NPJHOEFD_00070 | 2.6e-09 | S | Pfam:DUF955 | |||
NPJHOEFD_00071 | 3.8e-43 | L | Belongs to the 'phage' integrase family | |||
NPJHOEFD_00072 | 3.8e-220 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
NPJHOEFD_00073 | 4.4e-272 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
NPJHOEFD_00075 | 3.3e-208 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
NPJHOEFD_00076 | 2.1e-35 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
NPJHOEFD_00077 | 1.7e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
NPJHOEFD_00078 | 3.2e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
NPJHOEFD_00079 | 7e-45 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
NPJHOEFD_00080 | 3e-11 | ybhL | S | Belongs to the BI1 family | ||
NPJHOEFD_00081 | 6.8e-226 | I | Protein of unknown function (DUF2974) | |||
NPJHOEFD_00082 | 1.9e-116 | yhiD | S | MgtC family | ||
NPJHOEFD_00084 | 1.7e-148 | S | haloacid dehalogenase-like hydrolase | |||
NPJHOEFD_00085 | 7e-50 | |||||
NPJHOEFD_00086 | 7.1e-144 | 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 | |
NPJHOEFD_00087 | 5.4e-209 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NPJHOEFD_00088 | 4.8e-88 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NPJHOEFD_00089 | 1.8e-113 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
NPJHOEFD_00090 | 8e-210 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
NPJHOEFD_00091 | 1.4e-104 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
NPJHOEFD_00092 | 1.7e-232 | 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 | ||
NPJHOEFD_00093 | 5.8e-215 | 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 | ||
NPJHOEFD_00094 | 1.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
NPJHOEFD_00095 | 1.3e-148 | |||||
NPJHOEFD_00097 | 1.4e-43 | asnB | 6.3.5.4 | E | Asparagine synthase | |
NPJHOEFD_00098 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
NPJHOEFD_00099 | 4.9e-273 | S | Calcineurin-like phosphoesterase | |||
NPJHOEFD_00100 | 3.9e-84 | |||||
NPJHOEFD_00101 | 2.7e-120 | S | CAAX protease self-immunity | |||
NPJHOEFD_00102 | 5.6e-38 | ropB | K | Transcriptional regulator | ||
NPJHOEFD_00103 | 7.5e-52 | ropB | K | Transcriptional regulator | ||
NPJHOEFD_00104 | 6e-55 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
NPJHOEFD_00105 | 4.9e-228 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
NPJHOEFD_00106 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
NPJHOEFD_00107 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
NPJHOEFD_00108 | 9e-113 | 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 | ||
NPJHOEFD_00109 | 2.1e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
NPJHOEFD_00110 | 3.1e-47 | 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 | ||
NPJHOEFD_00111 | 3.6e-154 | 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 | ||
NPJHOEFD_00112 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
NPJHOEFD_00113 | 4e-54 | 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 | ||
NPJHOEFD_00114 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
NPJHOEFD_00115 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
NPJHOEFD_00116 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
NPJHOEFD_00117 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
NPJHOEFD_00118 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
NPJHOEFD_00119 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
NPJHOEFD_00120 | 5.7e-99 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
NPJHOEFD_00121 | 1.9e-259 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
NPJHOEFD_00122 | 3.3e-107 | |||||
NPJHOEFD_00123 | 5.8e-186 | XK27_05540 | S | DUF218 domain | ||
NPJHOEFD_00124 | 6.8e-170 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
NPJHOEFD_00125 | 3.4e-106 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NPJHOEFD_00126 | 6.6e-53 | cjaA | ET | ABC transporter substrate-binding protein | ||
NPJHOEFD_00127 | 8.1e-91 | cjaA | ET | ABC transporter substrate-binding protein | ||
NPJHOEFD_00128 | 2.3e-62 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
NPJHOEFD_00129 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
NPJHOEFD_00130 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
NPJHOEFD_00131 | 4.9e-75 | S | Peptidase propeptide and YPEB domain | |||
NPJHOEFD_00132 | 5.2e-187 | T | GHKL domain | |||
NPJHOEFD_00133 | 3.1e-130 | T | Transcriptional regulatory protein, C terminal | |||
NPJHOEFD_00134 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
NPJHOEFD_00135 | 2.9e-277 | V | ABC transporter transmembrane region | |||
NPJHOEFD_00136 | 6.4e-224 | S | Cysteine-rich secretory protein family | |||
NPJHOEFD_00137 | 2.6e-132 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NPJHOEFD_00138 | 1.3e-258 | glnPH2 | P | ABC transporter permease | ||
NPJHOEFD_00139 | 8e-68 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
NPJHOEFD_00140 | 8.3e-108 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
NPJHOEFD_00141 | 2.1e-134 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
NPJHOEFD_00142 | 2.8e-290 | |||||
NPJHOEFD_00144 | 3.3e-189 | cggR | K | Putative sugar-binding domain | ||
NPJHOEFD_00145 | 3.7e-174 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NPJHOEFD_00146 | 3e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
NPJHOEFD_00147 | 1.7e-142 | 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) | |
NPJHOEFD_00148 | 5.1e-17 | |||||
NPJHOEFD_00149 | 4.6e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
NPJHOEFD_00150 | 2.1e-55 | 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 | ||
NPJHOEFD_00151 | 1e-54 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NPJHOEFD_00152 | 6.4e-128 | K | UTRA domain | |||
NPJHOEFD_00153 | 1.3e-44 | ypsA | S | Belongs to the UPF0398 family | ||
NPJHOEFD_00154 | 1.1e-68 | 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 | ||
NPJHOEFD_00155 | 3.6e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
NPJHOEFD_00156 | 1e-242 | cpdA | S | Calcineurin-like phosphoesterase | ||
NPJHOEFD_00157 | 1.6e-155 | V | FtsX-like permease family | |||
NPJHOEFD_00158 | 4.7e-126 | yfnA | E | amino acid | ||
NPJHOEFD_00159 | 1.3e-273 | pipD | E | Dipeptidase | ||
NPJHOEFD_00160 | 1.1e-45 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
NPJHOEFD_00161 | 8.4e-287 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
NPJHOEFD_00162 | 1.7e-34 | |||||
NPJHOEFD_00163 | 1.2e-94 | sigH | K | Belongs to the sigma-70 factor family | ||
NPJHOEFD_00164 | 1.6e-60 | 3.6.1.55 | F | NUDIX domain | ||
NPJHOEFD_00165 | 1e-79 | S | AAA domain | |||
NPJHOEFD_00166 | 2.8e-115 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
NPJHOEFD_00167 | 1.9e-25 | |||||
NPJHOEFD_00168 | 0.0 | mco | Q | Multicopper oxidase | ||
NPJHOEFD_00169 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
NPJHOEFD_00170 | 2e-239 | oppA | E | ABC transporter | ||
NPJHOEFD_00171 | 6.1e-60 | oppA | E | ABC transporter | ||
NPJHOEFD_00172 | 2.2e-120 | lsa | S | ABC transporter | ||
NPJHOEFD_00173 | 4.3e-200 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
NPJHOEFD_00174 | 5.5e-155 | tilS | 2.4.2.8, 6.3.4.19 | J | 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 | |
NPJHOEFD_00175 | 1.3e-38 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
NPJHOEFD_00176 | 3.3e-161 | nusA | K | Participates in both transcription termination and antitermination | ||
NPJHOEFD_00178 | 1.5e-43 | ylxR | K | Protein of unknown function (DUF448) | ||
NPJHOEFD_00179 | 3.2e-47 | rplGA | J | ribosomal protein | ||
NPJHOEFD_00180 | 9.9e-82 | C | Flavodoxin | |||
NPJHOEFD_00181 | 0.0 | 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 | |
NPJHOEFD_00182 | 0.0 | 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 | |
NPJHOEFD_00183 | 1.6e-155 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
NPJHOEFD_00184 | 1.1e-59 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
NPJHOEFD_00185 | 2.2e-160 | 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 | ||
NPJHOEFD_00186 | 1.4e-87 | 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 | ||
NPJHOEFD_00187 | 6.7e-110 | rfbP | M | Bacterial sugar transferase | ||
NPJHOEFD_00188 | 1.4e-144 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NPJHOEFD_00189 | 1e-77 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
NPJHOEFD_00190 | 1.7e-23 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
NPJHOEFD_00191 | 1e-29 | epsB | M | biosynthesis protein | ||
NPJHOEFD_00192 | 1.1e-85 | epsB | M | biosynthesis protein | ||
NPJHOEFD_00193 | 1.6e-65 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NPJHOEFD_00194 | 4.7e-131 | V | ABC transporter transmembrane region | |||
NPJHOEFD_00195 | 1.4e-37 | S | Putative adhesin | |||
NPJHOEFD_00196 | 3.2e-101 | 3.6.1.27 | I | Acid phosphatase homologues | ||
NPJHOEFD_00197 | 2.5e-147 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
NPJHOEFD_00198 | 5.8e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
NPJHOEFD_00199 | 6.3e-33 | S | Domain of unknown function (DUF4767) | |||
NPJHOEFD_00200 | 7.6e-91 | F | Nucleoside 2-deoxyribosyltransferase | |||
NPJHOEFD_00201 | 5.2e-118 | |||||
NPJHOEFD_00204 | 3.6e-63 | |||||
NPJHOEFD_00205 | 2.3e-87 | S | Protein of unknown function (DUF805) | |||
NPJHOEFD_00206 | 2e-49 | O | OsmC-like protein | |||
NPJHOEFD_00207 | 9.4e-209 | EGP | Major facilitator Superfamily | |||
NPJHOEFD_00208 | 2.3e-99 | sptS | 2.7.13.3 | T | Histidine kinase | |
NPJHOEFD_00209 | 4.5e-94 | sptS | 2.7.13.3 | T | Histidine kinase | |
NPJHOEFD_00210 | 2.1e-23 | K | response regulator | |||
NPJHOEFD_00211 | 2.1e-255 | S | Archaea bacterial proteins of unknown function | |||
NPJHOEFD_00212 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
NPJHOEFD_00213 | 3.2e-131 | pepF | E | oligoendopeptidase F | ||
NPJHOEFD_00214 | 8.7e-197 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NPJHOEFD_00215 | 1.8e-111 | S | Protein of unknown function (DUF554) | |||
NPJHOEFD_00216 | 1.2e-30 | |||||
NPJHOEFD_00217 | 4.7e-120 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
NPJHOEFD_00218 | 3.4e-53 | |||||
NPJHOEFD_00220 | 4.6e-257 | pepC | 3.4.22.40 | E | aminopeptidase | |
NPJHOEFD_00221 | 1.1e-155 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_00222 | 3.7e-59 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
NPJHOEFD_00223 | 6.8e-31 | |||||
NPJHOEFD_00224 | 2.3e-78 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
NPJHOEFD_00225 | 3.2e-28 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
NPJHOEFD_00226 | 1e-218 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
NPJHOEFD_00227 | 2.1e-79 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
NPJHOEFD_00228 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NPJHOEFD_00229 | 2.3e-215 | mtlR | K | Mga helix-turn-helix domain | ||
NPJHOEFD_00230 | 2e-106 | K | Transcriptional regulator, AbiEi antitoxin | |||
NPJHOEFD_00231 | 7.6e-163 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
NPJHOEFD_00232 | 5.3e-189 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NPJHOEFD_00233 | 3.5e-145 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
NPJHOEFD_00234 | 9.4e-43 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
NPJHOEFD_00235 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NPJHOEFD_00236 | 6e-148 | |||||
NPJHOEFD_00237 | 1.9e-169 | |||||
NPJHOEFD_00238 | 3.7e-204 | glnA | 6.3.1.2 | E | glutamine synthetase | |
NPJHOEFD_00239 | 2e-226 | 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 | |
NPJHOEFD_00240 | 0.0 | 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 | |
NPJHOEFD_00241 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
NPJHOEFD_00242 | 1e-70 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
NPJHOEFD_00243 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
NPJHOEFD_00244 | 1.9e-46 | araD | 4.1.2.17, 5.1.3.4 | G | links the arabinose metabolic pathway to the pentose phosphate pathway and allows the bacteria to use arabinose as an energy source | |
NPJHOEFD_00245 | 5.2e-68 | L | haloacid dehalogenase-like hydrolase | |||
NPJHOEFD_00246 | 8.1e-38 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
NPJHOEFD_00247 | 5.7e-272 | P | Sodium:sulfate symporter transmembrane region | |||
NPJHOEFD_00248 | 5.8e-70 | hxlA | 6.2.1.3 | H | Aldolase/RraA | |
NPJHOEFD_00250 | 9.4e-33 | M | Peptidase family M23 | |||
NPJHOEFD_00251 | 1.2e-39 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
NPJHOEFD_00252 | 3.3e-127 | L | PFAM transposase IS116 IS110 IS902 | |||
NPJHOEFD_00253 | 1.3e-33 | C | 2Fe-2S iron-sulfur cluster binding domain | |||
NPJHOEFD_00254 | 5.1e-125 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00255 | 3e-37 | |||||
NPJHOEFD_00256 | 2.4e-110 | K | WHG domain | |||
NPJHOEFD_00257 | 6.4e-96 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
NPJHOEFD_00258 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
NPJHOEFD_00259 | 4e-175 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
NPJHOEFD_00260 | 2e-196 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
NPJHOEFD_00261 | 5.5e-36 | |||||
NPJHOEFD_00262 | 2.3e-130 | nadK | 2.7.1.23 | F | 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 | |
NPJHOEFD_00263 | 1e-170 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NPJHOEFD_00264 | 2.4e-84 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
NPJHOEFD_00265 | 7.2e-95 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NPJHOEFD_00266 | 3.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
NPJHOEFD_00267 | 5.7e-244 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
NPJHOEFD_00268 | 6.4e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
NPJHOEFD_00269 | 3.1e-107 | K | Transcriptional regulatory protein, C terminal | |||
NPJHOEFD_00270 | 1.1e-65 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
NPJHOEFD_00271 | 1.5e-102 | srtA | 3.4.22.70 | M | sortase family | |
NPJHOEFD_00272 | 2.5e-35 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
NPJHOEFD_00273 | 5.9e-24 | |||||
NPJHOEFD_00274 | 6.7e-146 | M | Glycosyl hydrolases family 25 | |||
NPJHOEFD_00275 | 6.9e-116 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
NPJHOEFD_00276 | 9.7e-52 | S | Iron-sulfur cluster assembly protein | |||
NPJHOEFD_00277 | 3.3e-130 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
NPJHOEFD_00278 | 1.3e-293 | fhaB | M | Rib/alpha-like repeat | ||
NPJHOEFD_00279 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
NPJHOEFD_00280 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
NPJHOEFD_00281 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
NPJHOEFD_00282 | 3.9e-81 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
NPJHOEFD_00283 | 9e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
NPJHOEFD_00284 | 6e-112 | |||||
NPJHOEFD_00286 | 1.7e-110 | E | Belongs to the SOS response-associated peptidase family | |||
NPJHOEFD_00287 | 3.7e-193 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NPJHOEFD_00288 | 4e-89 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
NPJHOEFD_00289 | 6.8e-96 | S | TPM domain | |||
NPJHOEFD_00290 | 5e-15 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NPJHOEFD_00291 | 3.4e-45 | oppA2 | E | ABC transporter, substratebinding protein | ||
NPJHOEFD_00292 | 6.5e-159 | oppA2 | E | ABC transporter, substratebinding protein | ||
NPJHOEFD_00293 | 2e-225 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
NPJHOEFD_00294 | 1.8e-212 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
NPJHOEFD_00295 | 3.8e-291 | 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 | ||
NPJHOEFD_00296 | 1.4e-110 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
NPJHOEFD_00298 | 2.4e-62 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
NPJHOEFD_00299 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
NPJHOEFD_00300 | 5e-22 | K | Acetyltransferase (GNAT) domain | |||
NPJHOEFD_00301 | 1.1e-223 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NPJHOEFD_00302 | 3.3e-275 | yjeM | E | Amino Acid | ||
NPJHOEFD_00303 | 5.8e-83 | S | Fic/DOC family | |||
NPJHOEFD_00304 | 5.2e-113 | |||||
NPJHOEFD_00305 | 5.7e-77 | K | LysR substrate binding domain | |||
NPJHOEFD_00306 | 8.4e-16 | |||||
NPJHOEFD_00307 | 1.1e-214 | S | Sterol carrier protein domain | |||
NPJHOEFD_00308 | 4.1e-133 | oppA | E | ABC transporter, substratebinding protein | ||
NPJHOEFD_00309 | 4.3e-64 | yrvN | L | AAA C-terminal domain | ||
NPJHOEFD_00310 | 1.7e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NPJHOEFD_00312 | 2.8e-47 | U | TraM recognition site of TraD and TraG | |||
NPJHOEFD_00313 | 8.3e-93 | sip | L | Belongs to the 'phage' integrase family | ||
NPJHOEFD_00314 | 6.2e-12 | |||||
NPJHOEFD_00315 | 5.6e-08 | M | Host cell surface-exposed lipoprotein | |||
NPJHOEFD_00317 | 8.8e-22 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_00318 | 1.4e-17 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_00319 | 2.2e-94 | S | DNA binding | |||
NPJHOEFD_00324 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
NPJHOEFD_00325 | 2.7e-61 | 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 | |
NPJHOEFD_00326 | 1.2e-144 | 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 | ||
NPJHOEFD_00327 | 2.1e-252 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
NPJHOEFD_00328 | 3.4e-91 | oppD | P | Belongs to the ABC transporter superfamily | ||
NPJHOEFD_00329 | 9.4e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
NPJHOEFD_00330 | 2e-238 | 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 | ||
NPJHOEFD_00331 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
NPJHOEFD_00332 | 9.7e-59 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
NPJHOEFD_00333 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
NPJHOEFD_00334 | 6.6e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
NPJHOEFD_00335 | 1.1e-110 | 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 | |
NPJHOEFD_00336 | 7.7e-30 | ropB | K | Helix-turn-helix domain | ||
NPJHOEFD_00337 | 9.7e-225 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NPJHOEFD_00338 | 2.2e-165 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NPJHOEFD_00339 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
NPJHOEFD_00340 | 4.3e-115 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NPJHOEFD_00341 | 9.7e-234 | cycA | E | Amino acid permease | ||
NPJHOEFD_00342 | 9.2e-248 | yifK | E | Amino acid permease | ||
NPJHOEFD_00343 | 6.4e-135 | S | PFAM Archaeal ATPase | |||
NPJHOEFD_00344 | 2.4e-172 | V | HNH endonuclease | |||
NPJHOEFD_00346 | 2e-137 | puuD | S | peptidase C26 | ||
NPJHOEFD_00347 | 1.8e-230 | steT_1 | E | amino acid | ||
NPJHOEFD_00348 | 3.2e-189 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
NPJHOEFD_00349 | 3.9e-206 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
NPJHOEFD_00352 | 7.7e-188 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
NPJHOEFD_00353 | 6.4e-251 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
NPJHOEFD_00354 | 6.2e-246 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
NPJHOEFD_00355 | 1e-105 | glnQ | 3.6.3.21 | E | ABC transporter | |
NPJHOEFD_00356 | 1.5e-107 | glnP | P | ABC transporter permease | ||
NPJHOEFD_00357 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
NPJHOEFD_00358 | 2.7e-124 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
NPJHOEFD_00359 | 2.5e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
NPJHOEFD_00360 | 5.7e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00361 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
NPJHOEFD_00362 | 1e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
NPJHOEFD_00363 | 1.6e-161 | htrA | 3.4.21.107 | O | serine protease | |
NPJHOEFD_00364 | 4.1e-147 | vicX | 3.1.26.11 | S | domain protein | |
NPJHOEFD_00365 | 3.4e-149 | yycI | S | YycH protein | ||
NPJHOEFD_00366 | 1.6e-257 | yycH | S | YycH protein | ||
NPJHOEFD_00367 | 1e-99 | 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 | |
NPJHOEFD_00368 | 8e-93 | tatD | L | hydrolase, TatD family | ||
NPJHOEFD_00369 | 5.8e-28 | tatD | L | hydrolase, TatD family | ||
NPJHOEFD_00370 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
NPJHOEFD_00371 | 1.8e-232 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NPJHOEFD_00372 | 3.8e-58 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NPJHOEFD_00373 | 1.9e-43 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NPJHOEFD_00374 | 5.5e-12 | qmcA | O | COG0330 Membrane protease subunits, stomatin prohibitin homologs | ||
NPJHOEFD_00375 | 3.5e-25 | qmcA | O | prohibitin homologues | ||
NPJHOEFD_00376 | 1.3e-34 | L | An automated process has identified a potential problem with this gene model | |||
NPJHOEFD_00377 | 1.5e-203 | pbg6 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NPJHOEFD_00378 | 2.2e-54 | V | ABC transporter | |||
NPJHOEFD_00380 | 9.6e-121 | K | response regulator | |||
NPJHOEFD_00381 | 2.1e-95 | oppA | E | ABC transporter substrate-binding protein | ||
NPJHOEFD_00382 | 1.2e-232 | oppA | E | ABC transporter substrate-binding protein | ||
NPJHOEFD_00383 | 2e-116 | isp2 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | ||
NPJHOEFD_00384 | 3.8e-191 | ftsZ | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
NPJHOEFD_00385 | 2.7e-111 | S | SLAP domain | |||
NPJHOEFD_00386 | 9.4e-177 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
NPJHOEFD_00387 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
NPJHOEFD_00388 | 8.7e-141 | 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 | |
NPJHOEFD_00389 | 2.1e-103 | S | Iron-sulfur cluster assembly protein | |||
NPJHOEFD_00390 | 1.5e-230 | XK27_04775 | S | PAS domain | ||
NPJHOEFD_00391 | 3e-210 | yttB | EGP | Major facilitator Superfamily | ||
NPJHOEFD_00392 | 1.3e-235 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NPJHOEFD_00393 | 2.9e-81 | D | Alpha beta | |||
NPJHOEFD_00394 | 2.7e-25 | D | Alpha beta | |||
NPJHOEFD_00395 | 1.8e-38 | D | Alpha beta | |||
NPJHOEFD_00396 | 8.8e-209 | M | Peptidase family M1 domain | |||
NPJHOEFD_00397 | 4e-30 | M | Peptidase family M1 domain | |||
NPJHOEFD_00398 | 1.2e-67 | S | Bacteriocin helveticin-J | |||
NPJHOEFD_00399 | 8.2e-96 | S | Bacteriocin helveticin-J | |||
NPJHOEFD_00400 | 8e-51 | L | RelB antitoxin | |||
NPJHOEFD_00401 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
NPJHOEFD_00402 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
NPJHOEFD_00403 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
NPJHOEFD_00404 | 1.1e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NPJHOEFD_00405 | 9.2e-158 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
NPJHOEFD_00406 | 2.9e-10 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
NPJHOEFD_00407 | 2e-104 | G | Transmembrane secretion effector | |||
NPJHOEFD_00408 | 4.5e-15 | G | Transmembrane secretion effector | |||
NPJHOEFD_00409 | 1.5e-144 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NPJHOEFD_00410 | 5.1e-292 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
NPJHOEFD_00411 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
NPJHOEFD_00412 | 9.4e-132 | comFC | S | Competence protein | ||
NPJHOEFD_00413 | 4.7e-246 | comFA | L | Helicase C-terminal domain protein | ||
NPJHOEFD_00414 | 5.1e-119 | yvyE | 3.4.13.9 | S | YigZ family | |
NPJHOEFD_00415 | 3e-207 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
NPJHOEFD_00416 | 7.4e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
NPJHOEFD_00417 | 4.2e-195 | 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 | ||
NPJHOEFD_00418 | 4.8e-63 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NPJHOEFD_00419 | 1.6e-208 | S | Tetratricopeptide repeat protein | |||
NPJHOEFD_00420 | 2.3e-41 | 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 | ||
NPJHOEFD_00421 | 6.6e-47 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
NPJHOEFD_00422 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
NPJHOEFD_00423 | 7.2e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
NPJHOEFD_00424 | 2e-121 | yjjP | S | Putative threonine/serine exporter | ||
NPJHOEFD_00426 | 5.7e-37 | M | domain protein | |||
NPJHOEFD_00427 | 1.1e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
NPJHOEFD_00428 | 2.9e-16 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
NPJHOEFD_00429 | 3.2e-77 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
NPJHOEFD_00430 | 1.1e-77 | 6.3.3.2 | S | ASCH | ||
NPJHOEFD_00431 | 7.5e-133 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NPJHOEFD_00432 | 4.1e-136 | |||||
NPJHOEFD_00433 | 1.9e-72 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
NPJHOEFD_00434 | 4.3e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
NPJHOEFD_00435 | 2e-13 | |||||
NPJHOEFD_00436 | 1.1e-39 | K | acetyltransferase | |||
NPJHOEFD_00437 | 5.7e-285 | pipD | E | Dipeptidase | ||
NPJHOEFD_00438 | 3.7e-156 | msmR | K | AraC-like ligand binding domain | ||
NPJHOEFD_00439 | 1.5e-223 | pbuX | F | xanthine permease | ||
NPJHOEFD_00440 | 9e-104 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
NPJHOEFD_00441 | 2.4e-43 | K | Helix-turn-helix | |||
NPJHOEFD_00442 | 7.8e-304 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
NPJHOEFD_00444 | 4.9e-99 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
NPJHOEFD_00445 | 1e-34 | clpE | O | Belongs to the ClpA ClpB family | ||
NPJHOEFD_00446 | 3.1e-262 | clpE | O | Belongs to the ClpA ClpB family | ||
NPJHOEFD_00447 | 1e-63 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
NPJHOEFD_00449 | 6.6e-61 | psiE | S | Phosphate-starvation-inducible E | ||
NPJHOEFD_00450 | 6.5e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
NPJHOEFD_00451 | 1.4e-18 | S | Iron-sulphur cluster biosynthesis | |||
NPJHOEFD_00452 | 1.1e-22 | K | AI-2E family transporter | |||
NPJHOEFD_00453 | 1.8e-59 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
NPJHOEFD_00454 | 4.1e-18 | |||||
NPJHOEFD_00455 | 4.1e-245 | G | Major Facilitator | |||
NPJHOEFD_00456 | 1.3e-79 | E | Zn peptidase | |||
NPJHOEFD_00457 | 1.2e-41 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
NPJHOEFD_00458 | 9.4e-30 | |||||
NPJHOEFD_00459 | 4.5e-66 | S | Bacteriocin helveticin-J | |||
NPJHOEFD_00460 | 1.7e-66 | S | SLAP domain | |||
NPJHOEFD_00461 | 5.8e-45 | |||||
NPJHOEFD_00462 | 2.4e-136 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00463 | 5.6e-121 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
NPJHOEFD_00464 | 1.7e-174 | ABC-SBP | S | ABC transporter | ||
NPJHOEFD_00465 | 5.6e-132 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
NPJHOEFD_00466 | 1.6e-48 | P | CorA-like Mg2+ transporter protein | |||
NPJHOEFD_00467 | 2.3e-257 | xylG | 3.6.3.17 | S | ABC transporter | |
NPJHOEFD_00468 | 4.7e-38 | |||||
NPJHOEFD_00469 | 3.3e-183 | 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) | |
NPJHOEFD_00470 | 8.4e-125 | luxT | K | Bacterial regulatory proteins, tetR family | ||
NPJHOEFD_00471 | 2.8e-135 | |||||
NPJHOEFD_00472 | 8.7e-138 | EGP | Major facilitator Superfamily | |||
NPJHOEFD_00473 | 1.5e-48 | |||||
NPJHOEFD_00474 | 2.6e-155 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
NPJHOEFD_00475 | 1.2e-40 | rusA | 3.1.22.4 | L | Endodeoxyribonuclease RusA | |
NPJHOEFD_00482 | 8.7e-34 | S | Transposase C of IS166 homeodomain | |||
NPJHOEFD_00483 | 9.3e-64 | L | PFAM IS66 Orf2 family protein | |||
NPJHOEFD_00484 | 7.7e-22 | |||||
NPJHOEFD_00485 | 7e-43 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
NPJHOEFD_00486 | 6.6e-182 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
NPJHOEFD_00487 | 9.7e-18 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
NPJHOEFD_00488 | 3.6e-229 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
NPJHOEFD_00489 | 2.2e-85 | uup | S | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00490 | 1.5e-201 | lctP | C | L-lactate permease | ||
NPJHOEFD_00491 | 3.1e-148 | glcU | U | sugar transport | ||
NPJHOEFD_00492 | 7.1e-46 | |||||
NPJHOEFD_00493 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
NPJHOEFD_00494 | 1e-43 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
NPJHOEFD_00495 | 5.4e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
NPJHOEFD_00496 | 2e-200 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
NPJHOEFD_00497 | 2.8e-199 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
NPJHOEFD_00499 | 1.4e-77 | Q | Imidazolonepropionase and related amidohydrolases | |||
NPJHOEFD_00500 | 8.5e-96 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
NPJHOEFD_00501 | 3e-53 | cvpA | S | Colicin V production protein | ||
NPJHOEFD_00503 | 7.5e-51 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
NPJHOEFD_00504 | 8.4e-265 | S | Fibronectin type III domain | |||
NPJHOEFD_00505 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00506 | 6.2e-276 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
NPJHOEFD_00507 | 9.5e-31 | |||||
NPJHOEFD_00508 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
NPJHOEFD_00509 | 6.4e-151 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
NPJHOEFD_00510 | 7.3e-208 | potD | P | ABC transporter | ||
NPJHOEFD_00511 | 1.2e-125 | potC | P | ABC transporter permease | ||
NPJHOEFD_00513 | 6.5e-18 | 2.7.1.200 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
NPJHOEFD_00514 | 1.1e-198 | gatC | G | PTS system sugar-specific permease component | ||
NPJHOEFD_00515 | 1.2e-24 | 2.7.1.200, 2.7.1.202 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system EIIA 2 | ||
NPJHOEFD_00517 | 5.6e-53 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
NPJHOEFD_00518 | 1.8e-73 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
NPJHOEFD_00519 | 3.6e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NPJHOEFD_00520 | 8.1e-175 | ulaG | S | Beta-lactamase superfamily domain | ||
NPJHOEFD_00521 | 1.5e-61 | cmtB | 2.7.1.194, 2.7.1.197, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
NPJHOEFD_00522 | 6.3e-52 | ulaA | S | PTS system sugar-specific permease component | ||
NPJHOEFD_00523 | 3e-99 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NPJHOEFD_00524 | 3.4e-73 | metI | P | ABC transporter permease | ||
NPJHOEFD_00525 | 1.6e-81 | EGP | Major facilitator Superfamily | |||
NPJHOEFD_00526 | 4e-150 | 3.1.3.102, 3.1.3.104 | S | haloacid dehalogenase-like hydrolase | ||
NPJHOEFD_00527 | 0.0 | tetP | J | elongation factor G | ||
NPJHOEFD_00528 | 3.5e-160 | yvgN | C | Aldo keto reductase | ||
NPJHOEFD_00529 | 2.8e-134 | G | Bacterial extracellular solute-binding protein | |||
NPJHOEFD_00530 | 6.3e-178 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NPJHOEFD_00531 | 3.5e-27 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NPJHOEFD_00532 | 5.6e-86 | |||||
NPJHOEFD_00533 | 1.9e-156 | S | Protein of unknown function (DUF2974) | |||
NPJHOEFD_00534 | 2.4e-84 | glnP | P | ABC transporter permease | ||
NPJHOEFD_00535 | 9.3e-86 | |||||
NPJHOEFD_00536 | 2.5e-283 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NPJHOEFD_00537 | 8.5e-181 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NPJHOEFD_00538 | 3e-147 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NPJHOEFD_00539 | 4.4e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
NPJHOEFD_00540 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
NPJHOEFD_00541 | 1.2e-54 | oppA | E | ABC transporter, substratebinding protein | ||
NPJHOEFD_00542 | 3.1e-209 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
NPJHOEFD_00543 | 1.1e-146 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NPJHOEFD_00544 | 8e-188 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NPJHOEFD_00545 | 1.6e-79 | |||||
NPJHOEFD_00546 | 3.4e-155 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
NPJHOEFD_00547 | 9.7e-137 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
NPJHOEFD_00548 | 1.6e-36 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
NPJHOEFD_00549 | 1.2e-189 | ytgP | S | Polysaccharide biosynthesis protein | ||
NPJHOEFD_00550 | 1.9e-36 | |||||
NPJHOEFD_00551 | 1.2e-203 | XK27_06780 | V | ABC transporter permease | ||
NPJHOEFD_00552 | 5.3e-90 | ecfT | U | Transmembrane (T) component of an 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 | ||
NPJHOEFD_00553 | 4.8e-148 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
NPJHOEFD_00554 | 6.5e-78 | 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 | ||
NPJHOEFD_00555 | 5.1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
NPJHOEFD_00556 | 8.9e-133 | L | Phage integrase family | |||
NPJHOEFD_00557 | 1.3e-42 | |||||
NPJHOEFD_00558 | 1.9e-75 | M | LysM domain | |||
NPJHOEFD_00559 | 3.5e-199 | pbpX | V | Beta-lactamase | ||
NPJHOEFD_00560 | 2.7e-252 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NPJHOEFD_00561 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
NPJHOEFD_00569 | 1.2e-256 | emrY | EGP | Major facilitator Superfamily | ||
NPJHOEFD_00570 | 1.8e-158 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
NPJHOEFD_00573 | 5.2e-61 | S | cog cog0433 | |||
NPJHOEFD_00574 | 1.1e-14 | mrr | L | restriction endonuclease | ||
NPJHOEFD_00575 | 1.9e-110 | F | DNA/RNA non-specific endonuclease | |||
NPJHOEFD_00576 | 2.7e-34 | S | YSIRK type signal peptide | |||
NPJHOEFD_00578 | 5.5e-53 | |||||
NPJHOEFD_00579 | 1.1e-116 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
NPJHOEFD_00580 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
NPJHOEFD_00581 | 1.1e-103 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
NPJHOEFD_00582 | 1.3e-54 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
NPJHOEFD_00583 | 4.7e-25 | S | Protein conserved in bacteria | |||
NPJHOEFD_00584 | 3.9e-57 | |||||
NPJHOEFD_00585 | 4.7e-85 | |||||
NPJHOEFD_00586 | 4.6e-88 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
NPJHOEFD_00587 | 1.7e-48 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
NPJHOEFD_00588 | 2.2e-171 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
NPJHOEFD_00589 | 2.2e-24 | yeaE | S | Aldo/keto reductase family | ||
NPJHOEFD_00590 | 2.4e-167 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
NPJHOEFD_00591 | 1.2e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
NPJHOEFD_00592 | 6.9e-195 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
NPJHOEFD_00593 | 1.8e-95 | ydjP | I | Alpha/beta hydrolase family | ||
NPJHOEFD_00594 | 7.1e-138 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NPJHOEFD_00595 | 5.8e-35 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
NPJHOEFD_00596 | 1.4e-78 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
NPJHOEFD_00597 | 2.2e-85 | S | PFAM Archaeal ATPase | |||
NPJHOEFD_00598 | 5.7e-84 | S | PFAM Archaeal ATPase | |||
NPJHOEFD_00599 | 7.7e-26 | |||||
NPJHOEFD_00600 | 2.3e-43 | ybhL | S | Belongs to the BI1 family | ||
NPJHOEFD_00601 | 1.2e-210 | S | Bacterial protein of unknown function (DUF871) | |||
NPJHOEFD_00602 | 9.9e-217 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
NPJHOEFD_00603 | 1.3e-46 | lysR5 | K | LysR substrate binding domain | ||
NPJHOEFD_00604 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
NPJHOEFD_00605 | 2.9e-262 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NPJHOEFD_00607 | 1.2e-92 | S | AntA/AntB antirepressor | |||
NPJHOEFD_00608 | 4.3e-15 | |||||
NPJHOEFD_00610 | 3e-10 | |||||
NPJHOEFD_00612 | 4.7e-45 | 3.4.21.88 | K | Peptidase S24-like | ||
NPJHOEFD_00616 | 1.6e-20 | S | YjcQ protein | |||
NPJHOEFD_00617 | 1.2e-171 | sip | L | Belongs to the 'phage' integrase family | ||
NPJHOEFD_00618 | 8.1e-126 | S | PAS domain | |||
NPJHOEFD_00619 | 6e-11 | |||||
NPJHOEFD_00621 | 4.2e-308 | E | Amino acid permease | |||
NPJHOEFD_00622 | 8.2e-48 | 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 | ||
NPJHOEFD_00623 | 3.5e-179 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
NPJHOEFD_00627 | 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 | ||
NPJHOEFD_00628 | 1.3e-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 | ||
NPJHOEFD_00629 | 7.8e-70 | 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 | ||
NPJHOEFD_00630 | 1.2e-115 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
NPJHOEFD_00631 | 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 | |
NPJHOEFD_00632 | 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 | |
NPJHOEFD_00633 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
NPJHOEFD_00634 | 3.5e-75 | |||||
NPJHOEFD_00635 | 2.3e-181 | M | CHAP domain | |||
NPJHOEFD_00636 | 6.3e-304 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
NPJHOEFD_00637 | 1.7e-304 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
NPJHOEFD_00638 | 1.6e-182 | 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 | |
NPJHOEFD_00639 | 1.9e-104 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NPJHOEFD_00640 | 1.3e-36 | |||||
NPJHOEFD_00641 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
NPJHOEFD_00642 | 2.8e-162 | M | NlpC/P60 family | |||
NPJHOEFD_00643 | 6.5e-91 | G | Peptidase_C39 like family | |||
NPJHOEFD_00644 | 1.7e-173 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
NPJHOEFD_00645 | 2.8e-77 | P | Cobalt transport protein | |||
NPJHOEFD_00646 | 4.8e-249 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00647 | 7.9e-174 | K | helix_turn_helix, arabinose operon control protein | |||
NPJHOEFD_00648 | 8.3e-157 | htpX | O | Belongs to the peptidase M48B family | ||
NPJHOEFD_00649 | 5.1e-96 | lemA | S | LemA family | ||
NPJHOEFD_00650 | 7.5e-192 | ybiR | P | Citrate transporter | ||
NPJHOEFD_00651 | 2.9e-29 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
NPJHOEFD_00652 | 1.3e-12 | L | TIGRFAM transposase, IS605 OrfB family | |||
NPJHOEFD_00653 | 1.2e-11 | S | Transposase C of IS166 homeodomain | |||
NPJHOEFD_00654 | 1.4e-59 | XK27_01125 | L | IS66 Orf2 like protein | ||
NPJHOEFD_00655 | 4.4e-169 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
NPJHOEFD_00656 | 1.6e-70 | K | Transcriptional regulator | |||
NPJHOEFD_00657 | 4.5e-117 | 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 | ||
NPJHOEFD_00658 | 2.2e-89 | |||||
NPJHOEFD_00659 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
NPJHOEFD_00660 | 6.3e-123 | M | Iron Transport-associated domain | |||
NPJHOEFD_00661 | 8.7e-159 | isdE | P | Periplasmic binding protein | ||
NPJHOEFD_00662 | 9.5e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NPJHOEFD_00663 | 6.7e-139 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
NPJHOEFD_00664 | 6.7e-44 | 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 | ||
NPJHOEFD_00665 | 1e-50 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
NPJHOEFD_00666 | 1.3e-38 | S | RelB antitoxin | |||
NPJHOEFD_00667 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
NPJHOEFD_00668 | 1.8e-206 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
NPJHOEFD_00669 | 1.8e-98 | murB | 1.3.1.98 | M | Cell wall formation | |
NPJHOEFD_00670 | 2.8e-41 | murB | 1.3.1.98 | M | Cell wall formation | |
NPJHOEFD_00671 | 1.7e-37 | L | Transposase and inactivated derivatives, IS30 family | |||
NPJHOEFD_00672 | 4.6e-171 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
NPJHOEFD_00673 | 7.3e-294 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
NPJHOEFD_00674 | 3.2e-23 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
NPJHOEFD_00675 | 1.6e-08 | |||||
NPJHOEFD_00676 | 1.4e-83 | K | FR47-like protein | |||
NPJHOEFD_00677 | 1.1e-297 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NPJHOEFD_00678 | 2e-194 | 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 | ||
NPJHOEFD_00679 | 9.7e-166 | 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 | ||
NPJHOEFD_00680 | 2.4e-34 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NPJHOEFD_00681 | 1.1e-161 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
NPJHOEFD_00682 | 2.4e-231 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
NPJHOEFD_00683 | 6.2e-43 | 1.3.5.4 | C | FAD binding domain | ||
NPJHOEFD_00684 | 8.8e-84 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NPJHOEFD_00685 | 2.8e-168 | K | LysR substrate binding domain | |||
NPJHOEFD_00686 | 1.1e-121 | 3.6.1.27 | I | Acid phosphatase homologues | ||
NPJHOEFD_00687 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NPJHOEFD_00688 | 1.8e-62 | yabR | J | S1 RNA binding domain | ||
NPJHOEFD_00689 | 5.6e-57 | divIC | D | Septum formation initiator | ||
NPJHOEFD_00690 | 1.6e-33 | yabO | J | S4 domain protein | ||
NPJHOEFD_00691 | 1.2e-294 | 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 | ||
NPJHOEFD_00692 | 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 | ||
NPJHOEFD_00693 | 5.1e-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 | |
NPJHOEFD_00694 | 1.5e-183 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NPJHOEFD_00699 | 1.8e-07 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_00700 | 7.2e-10 | |||||
NPJHOEFD_00702 | 7.8e-178 | M | Glycosyl hydrolases family 25 | |||
NPJHOEFD_00703 | 3.3e-259 | lmrB | EGP | Major facilitator Superfamily | ||
NPJHOEFD_00704 | 4e-251 | I | Protein of unknown function (DUF2974) | |||
NPJHOEFD_00705 | 4e-177 | G | Glycosyl hydrolases family 8 | |||
NPJHOEFD_00706 | 4.5e-189 | ydaM | M | Glycosyl transferase | ||
NPJHOEFD_00707 | 1.1e-07 | S | Uncharacterised protein family (UPF0236) | |||
NPJHOEFD_00708 | 1.2e-17 | |||||
NPJHOEFD_00709 | 7.2e-83 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
NPJHOEFD_00710 | 7.8e-38 | |||||
NPJHOEFD_00711 | 2e-32 | |||||
NPJHOEFD_00712 | 7.9e-135 | EG | EamA-like transporter family | |||
NPJHOEFD_00713 | 2.6e-61 | M | Glycosyl hydrolases family 25 | |||
NPJHOEFD_00714 | 1.3e-61 | M | Glycosyl hydrolases family 25 | |||
NPJHOEFD_00715 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
NPJHOEFD_00716 | 4.7e-249 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NPJHOEFD_00718 | 9.2e-65 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
NPJHOEFD_00719 | 2.8e-100 | S | ECF transporter, substrate-specific component | |||
NPJHOEFD_00720 | 2.4e-79 | npr | 1.11.1.1 | C | NADH oxidase | |
NPJHOEFD_00721 | 6.6e-11 | |||||
NPJHOEFD_00722 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
NPJHOEFD_00723 | 5.3e-167 | slpX | S | SLAP domain | ||
NPJHOEFD_00724 | 4.8e-44 | slpX | S | SLAP domain | ||
NPJHOEFD_00725 | 3.7e-143 | K | SIS domain | |||
NPJHOEFD_00726 | 8.1e-120 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
NPJHOEFD_00727 | 2.7e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
NPJHOEFD_00728 | 6.5e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
NPJHOEFD_00729 | 4.7e-117 | S | Protein of unknown function (DUF1351) | |||
NPJHOEFD_00730 | 4.6e-45 | |||||
NPJHOEFD_00732 | 5.5e-18 | |||||
NPJHOEFD_00733 | 5.1e-27 | S | Helix-turn-helix domain | |||
NPJHOEFD_00734 | 1.9e-253 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
NPJHOEFD_00735 | 5.7e-69 | rplI | J | Binds to the 23S rRNA | ||
NPJHOEFD_00736 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
NPJHOEFD_00737 | 1.5e-50 | |||||
NPJHOEFD_00738 | 5.5e-09 | |||||
NPJHOEFD_00739 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
NPJHOEFD_00740 | 1.5e-95 | S | UPF0397 protein | |||
NPJHOEFD_00741 | 4.1e-90 | S | Short repeat of unknown function (DUF308) | |||
NPJHOEFD_00742 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
NPJHOEFD_00743 | 9.7e-186 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
NPJHOEFD_00744 | 2.1e-171 | whiA | K | May be required for sporulation | ||
NPJHOEFD_00745 | 2.3e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
NPJHOEFD_00746 | 0.0 | S | SH3-like domain | |||
NPJHOEFD_00747 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00748 | 2.4e-190 | pts23C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NPJHOEFD_00749 | 1.5e-31 | lacE | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NPJHOEFD_00751 | 8.4e-31 | |||||
NPJHOEFD_00752 | 3e-21 | |||||
NPJHOEFD_00753 | 3.7e-83 | |||||
NPJHOEFD_00754 | 8.2e-31 | yozG | K | Transcriptional regulator | ||
NPJHOEFD_00755 | 2e-23 | |||||
NPJHOEFD_00756 | 1.7e-67 | |||||
NPJHOEFD_00757 | 1.7e-19 | |||||
NPJHOEFD_00758 | 5.6e-258 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NPJHOEFD_00759 | 2.7e-74 | K | Helix-turn-helix domain | |||
NPJHOEFD_00760 | 1.5e-25 | S | CAAX protease self-immunity | |||
NPJHOEFD_00761 | 1.4e-22 | S | CAAX protease self-immunity | |||
NPJHOEFD_00762 | 7.6e-26 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
NPJHOEFD_00764 | 1.6e-96 | ybaT | E | Amino acid permease | ||
NPJHOEFD_00765 | 1.7e-07 | S | LPXTG cell wall anchor motif | |||
NPJHOEFD_00766 | 4.4e-146 | S | Putative ABC-transporter type IV | |||
NPJHOEFD_00770 | 2.2e-82 | uspA | T | universal stress protein | ||
NPJHOEFD_00771 | 7.5e-149 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
NPJHOEFD_00772 | 8.6e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NPJHOEFD_00773 | 3.1e-29 | ntd | 2.4.2.6 | F | Nucleoside | |
NPJHOEFD_00774 | 5.2e-08 | |||||
NPJHOEFD_00775 | 1.4e-245 | P | P-loop Domain of unknown function (DUF2791) | |||
NPJHOEFD_00776 | 2.6e-138 | S | TerB-C domain | |||
NPJHOEFD_00777 | 6.4e-232 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
NPJHOEFD_00778 | 2.1e-42 | |||||
NPJHOEFD_00779 | 1.4e-51 | |||||
NPJHOEFD_00780 | 1.4e-184 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
NPJHOEFD_00781 | 4.8e-51 | L | HNH nucleases | |||
NPJHOEFD_00782 | 6.9e-132 | S | Protein of unknown function (DUF805) | |||
NPJHOEFD_00783 | 3.4e-135 | glnQ | E | ABC transporter, ATP-binding protein | ||
NPJHOEFD_00784 | 6.7e-290 | glnP | P | ABC transporter permease | ||
NPJHOEFD_00785 | 4e-121 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
NPJHOEFD_00786 | 5.8e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
NPJHOEFD_00787 | 8.2e-104 | terC | P | Integral membrane protein TerC family | ||
NPJHOEFD_00788 | 9.2e-92 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
NPJHOEFD_00789 | 2.8e-69 | cobB | K | SIR2 family | ||
NPJHOEFD_00790 | 2.5e-68 | |||||
NPJHOEFD_00791 | 2.7e-134 | yvpB | S | Peptidase_C39 like family | ||
NPJHOEFD_00792 | 1.1e-83 | S | Threonine/Serine exporter, ThrE | |||
NPJHOEFD_00793 | 2.4e-136 | thrE | S | Putative threonine/serine exporter | ||
NPJHOEFD_00794 | 8.9e-292 | S | ABC transporter | |||
NPJHOEFD_00795 | 8.3e-58 | |||||
NPJHOEFD_00796 | 5e-72 | rimL | J | Acetyltransferase (GNAT) domain | ||
NPJHOEFD_00797 | 9.7e-55 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
NPJHOEFD_00798 | 1.4e-30 | |||||
NPJHOEFD_00799 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
NPJHOEFD_00800 | 4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
NPJHOEFD_00801 | 4.2e-303 | yloV | S | DAK2 domain fusion protein YloV | ||
NPJHOEFD_00802 | 0.0 | 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) | |
NPJHOEFD_00803 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
NPJHOEFD_00804 | 3.3e-240 | 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 | |
NPJHOEFD_00805 | 8.9e-173 | 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 | ||
NPJHOEFD_00806 | 6.8e-150 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
NPJHOEFD_00807 | 7.3e-44 | |||||
NPJHOEFD_00808 | 5.4e-183 | S | AAA domain | |||
NPJHOEFD_00809 | 2.6e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NPJHOEFD_00810 | 1.4e-23 | |||||
NPJHOEFD_00811 | 7.3e-161 | czcD | P | cation diffusion facilitator family transporter | ||
NPJHOEFD_00812 | 1.1e-98 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
NPJHOEFD_00814 | 2.8e-154 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
NPJHOEFD_00815 | 1.3e-240 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NPJHOEFD_00817 | 4.7e-46 | pspC | KT | PspC domain | ||
NPJHOEFD_00818 | 1.8e-224 | L | COG2963 Transposase and inactivated derivatives | |||
NPJHOEFD_00819 | 2.9e-116 | plsC | 2.3.1.51 | I | Acyltransferase | |
NPJHOEFD_00820 | 7.2e-217 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
NPJHOEFD_00821 | 2.1e-75 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
NPJHOEFD_00822 | 1.3e-70 | rplO | J | Binds to the 23S rRNA | ||
NPJHOEFD_00823 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
NPJHOEFD_00824 | 4.1e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
NPJHOEFD_00825 | 3.6e-55 | 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 | ||
NPJHOEFD_00826 | 1.1e-50 | 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 | ||
NPJHOEFD_00827 | 4.3e-86 | 3.4.21.96 | S | SLAP domain | ||
NPJHOEFD_00828 | 9.7e-158 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
NPJHOEFD_00829 | 1.1e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
NPJHOEFD_00830 | 9.1e-30 | hlyIII | S | protein, hemolysin III | ||
NPJHOEFD_00831 | 5.9e-62 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
NPJHOEFD_00832 | 6.8e-22 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
NPJHOEFD_00833 | 2.7e-255 | 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 | ||
NPJHOEFD_00834 | 3.2e-286 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
NPJHOEFD_00835 | 1.5e-25 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
NPJHOEFD_00836 | 5.5e-41 | |||||
NPJHOEFD_00837 | 2.1e-161 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NPJHOEFD_00838 | 1.7e-106 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
NPJHOEFD_00839 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
NPJHOEFD_00840 | 6.5e-180 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
NPJHOEFD_00841 | 5.4e-215 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
NPJHOEFD_00843 | 2.2e-134 | 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 | ||
NPJHOEFD_00844 | 7.3e-74 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
NPJHOEFD_00845 | 1.7e-45 | yggT | S | YGGT family | ||
NPJHOEFD_00846 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
NPJHOEFD_00847 | 5.8e-52 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
NPJHOEFD_00848 | 8.7e-253 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
NPJHOEFD_00849 | 2.6e-157 | S | Sucrose-6F-phosphate phosphohydrolase | |||
NPJHOEFD_00850 | 3.2e-55 | ybeC | E | amino acid | ||
NPJHOEFD_00851 | 7.5e-231 | pbuG | S | permease | ||
NPJHOEFD_00852 | 2.5e-119 | K | helix_turn_helix, mercury resistance | |||
NPJHOEFD_00853 | 3.3e-37 | |||||
NPJHOEFD_00854 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
NPJHOEFD_00855 | 1.9e-65 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
NPJHOEFD_00856 | 8.3e-131 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
NPJHOEFD_00857 | 1.4e-158 | coiA | 3.6.4.12 | S | Competence protein | |
NPJHOEFD_00858 | 4.6e-114 | yjbH | Q | Thioredoxin | ||
NPJHOEFD_00859 | 1.7e-108 | yjbK | S | CYTH | ||
NPJHOEFD_00860 | 2.5e-37 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
NPJHOEFD_00861 | 1.9e-116 | potE | E | amino acid | ||
NPJHOEFD_00862 | 9.6e-76 | potE | E | amino acid | ||
NPJHOEFD_00863 | 1.6e-111 | plsY | 2.3.1.15 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
NPJHOEFD_00864 | 2.7e-202 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NPJHOEFD_00865 | 1.4e-98 | G | Aldose 1-epimerase | |||
NPJHOEFD_00866 | 5e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NPJHOEFD_00867 | 2.1e-116 | |||||
NPJHOEFD_00868 | 9.9e-129 | potA11 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
NPJHOEFD_00869 | 4.1e-15 | M | Lysin motif | |||
NPJHOEFD_00870 | 2.2e-114 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
NPJHOEFD_00871 | 1.4e-147 | S | hydrolase | |||
NPJHOEFD_00872 | 3.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
NPJHOEFD_00873 | 8.7e-125 | ybbR | S | YbbR-like protein | ||
NPJHOEFD_00874 | 0.0 | typA | T | GTP-binding protein TypA | ||
NPJHOEFD_00875 | 1.3e-72 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
NPJHOEFD_00876 | 7e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
NPJHOEFD_00877 | 4.4e-135 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
NPJHOEFD_00878 | 2.7e-114 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
NPJHOEFD_00879 | 8.7e-42 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
NPJHOEFD_00880 | 1e-235 | G | Bacterial extracellular solute-binding protein | |||
NPJHOEFD_00881 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
NPJHOEFD_00882 | 2.1e-174 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
NPJHOEFD_00884 | 3.5e-84 | lacR | K | Transcriptional regulator | ||
NPJHOEFD_00885 | 3e-58 | lacR | K | Transcriptional regulator | ||
NPJHOEFD_00886 | 5.8e-68 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
NPJHOEFD_00887 | 1.1e-139 | stp | 3.1.3.16 | T | phosphatase | |
NPJHOEFD_00889 | 4.2e-43 | |||||
NPJHOEFD_00890 | 2e-94 | S | Protein of unknown function (DUF3990) | |||
NPJHOEFD_00891 | 4.4e-121 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
NPJHOEFD_00892 | 4.9e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
NPJHOEFD_00893 | 3e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
NPJHOEFD_00894 | 1.3e-47 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
NPJHOEFD_00895 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
NPJHOEFD_00896 | 3.7e-151 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
NPJHOEFD_00897 | 7.8e-255 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NPJHOEFD_00899 | 7.8e-270 | S | Predicted membrane protein (DUF2207) | |||
NPJHOEFD_00900 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
NPJHOEFD_00901 | 4.5e-92 | dnaI | L | Primosomal protein DnaI | ||
NPJHOEFD_00902 | 4.4e-62 | dnaI | L | Primosomal protein DnaI | ||
NPJHOEFD_00903 | 9.2e-107 | dnaB | L | Replication initiation and membrane attachment | ||
NPJHOEFD_00904 | 8.5e-134 | dnaB | L | Replication initiation and membrane attachment | ||
NPJHOEFD_00905 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
NPJHOEFD_00906 | 2.8e-216 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
NPJHOEFD_00907 | 4.8e-34 | S | reductase | |||
NPJHOEFD_00908 | 4.4e-39 | S | reductase | |||
NPJHOEFD_00909 | 2.7e-32 | S | reductase | |||
NPJHOEFD_00910 | 9.6e-135 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
NPJHOEFD_00911 | 5e-141 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
NPJHOEFD_00912 | 1.9e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
NPJHOEFD_00913 | 1.9e-34 | yitW | S | Iron-sulfur cluster assembly protein | ||
NPJHOEFD_00914 | 7.5e-247 | sufB | O | assembly protein SufB | ||
NPJHOEFD_00915 | 1.4e-53 | nifU | C | SUF system FeS assembly protein, NifU family | ||
NPJHOEFD_00916 | 3e-112 | L | PFAM transposase IS116 IS110 IS902 | |||
NPJHOEFD_00917 | 2.3e-48 | S | SLAP domain | |||
NPJHOEFD_00918 | 2.9e-130 | S | SLAP domain | |||
NPJHOEFD_00919 | 9.4e-130 | |||||
NPJHOEFD_00920 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
NPJHOEFD_00921 | 2e-160 | rssA | S | Phospholipase, patatin family | ||
NPJHOEFD_00922 | 5.4e-147 | S | hydrolase | |||
NPJHOEFD_00923 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
NPJHOEFD_00924 | 3.3e-147 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NPJHOEFD_00925 | 1.6e-80 | |||||
NPJHOEFD_00926 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
NPJHOEFD_00927 | 2.1e-39 | |||||
NPJHOEFD_00928 | 1.9e-118 | C | nitroreductase | |||
NPJHOEFD_00929 | 1.7e-213 | 1.3.5.4 | C | FAD binding domain | ||
NPJHOEFD_00930 | 1.2e-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 | ||
NPJHOEFD_00931 | 4.5e-78 | 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 | ||
NPJHOEFD_00932 | 9.4e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
NPJHOEFD_00933 | 0.0 | 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 | |
NPJHOEFD_00934 | 1.5e-46 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
NPJHOEFD_00935 | 4e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
NPJHOEFD_00936 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
NPJHOEFD_00937 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
NPJHOEFD_00938 | 1.5e-167 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
NPJHOEFD_00939 | 2.9e-224 | ynbB | 4.4.1.1 | P | aluminum resistance | |
NPJHOEFD_00940 | 4.2e-53 | K | LytTr DNA-binding domain | |||
NPJHOEFD_00941 | 7.7e-39 | S | Protein of unknown function (DUF3021) | |||
NPJHOEFD_00942 | 6.1e-269 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NPJHOEFD_00943 | 1.2e-127 | K | LytTr DNA-binding domain | |||
NPJHOEFD_00944 | 5.6e-134 | 2.7.13.3 | T | GHKL domain | ||
NPJHOEFD_00945 | 2.6e-169 | nhaC | C | Na H antiporter NhaC | ||
NPJHOEFD_00946 | 1.4e-147 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
NPJHOEFD_00947 | 2.6e-57 | |||||
NPJHOEFD_00948 | 6.4e-153 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
NPJHOEFD_00949 | 1.5e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
NPJHOEFD_00951 | 1.3e-21 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
NPJHOEFD_00954 | 2e-26 | S | Domain of unknown function (DUF771) | |||
NPJHOEFD_00956 | 4.3e-52 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
NPJHOEFD_00957 | 6.7e-48 | pbuG | S | permease | ||
NPJHOEFD_00958 | 3.5e-56 | S | ABC-2 family transporter protein | |||
NPJHOEFD_00959 | 4.7e-60 | S | ABC-2 family transporter protein | |||
NPJHOEFD_00960 | 2.4e-92 | V | ABC transporter, ATP-binding protein | |||
NPJHOEFD_00961 | 4e-98 | rihB | 3.2.2.1 | F | Nucleoside | |
NPJHOEFD_00962 | 3.2e-72 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
NPJHOEFD_00963 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
NPJHOEFD_00964 | 3e-57 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
NPJHOEFD_00965 | 6.9e-152 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
NPJHOEFD_00966 | 8.1e-183 | tnpB | L | Putative transposase DNA-binding domain | ||
NPJHOEFD_00967 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
NPJHOEFD_00968 | 4.4e-200 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
NPJHOEFD_00969 | 4.4e-123 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
NPJHOEFD_00970 | 4.3e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
NPJHOEFD_00971 | 5.3e-59 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
NPJHOEFD_00972 | 1.7e-215 | ylbM | S | Belongs to the UPF0348 family | ||
NPJHOEFD_00973 | 3e-96 | yceD | S | Uncharacterized ACR, COG1399 | ||
NPJHOEFD_00974 | 1.2e-126 | K | response regulator | |||
NPJHOEFD_00975 | 3.4e-68 | aatB | ET | ABC transporter substrate-binding protein | ||
NPJHOEFD_00976 | 7.5e-74 | yjcF | S | Acetyltransferase (GNAT) domain | ||
NPJHOEFD_00977 | 7.1e-98 | E | GDSL-like Lipase/Acylhydrolase | |||
NPJHOEFD_00978 | 2.5e-169 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NPJHOEFD_00979 | 3.9e-139 | 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 | |
NPJHOEFD_00980 | 3.3e-135 | 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 | |
NPJHOEFD_00981 | 1.8e-151 | pstA | P | Phosphate transport system permease protein PstA | ||
NPJHOEFD_00982 | 1.9e-162 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
NPJHOEFD_00983 | 2.8e-157 | pstS | P | Phosphate | ||
NPJHOEFD_00984 | 1.6e-67 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
NPJHOEFD_00985 | 7.2e-77 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
NPJHOEFD_00986 | 5.2e-148 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
NPJHOEFD_00987 | 2.2e-76 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
NPJHOEFD_00988 | 1.5e-95 | mepA | V | MATE efflux family protein | ||
NPJHOEFD_00989 | 6.4e-176 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
NPJHOEFD_00990 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
NPJHOEFD_00991 | 3.4e-103 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NPJHOEFD_00992 | 1.8e-167 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
NPJHOEFD_00993 | 1.1e-135 | V | ABC transporter transmembrane region | |||
NPJHOEFD_00994 | 5.2e-170 | degV | S | DegV family | ||
NPJHOEFD_00995 | 9.6e-164 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
NPJHOEFD_00996 | 8.6e-24 | ywzB | S | Protein of unknown function (DUF1146) | ||
NPJHOEFD_00997 | 1.2e-177 | mbl | D | Cell shape determining protein MreB Mrl | ||
NPJHOEFD_00998 | 1e-50 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
NPJHOEFD_00999 | 2.8e-28 | S | Protein of unknown function (DUF2969) | |||
NPJHOEFD_01000 | 4.7e-216 | rodA | D | Belongs to the SEDS family | ||
NPJHOEFD_01001 | 1.8e-78 | usp6 | T | universal stress protein | ||
NPJHOEFD_01002 | 8.4e-39 | |||||
NPJHOEFD_01003 | 3.5e-106 | rarA | L | recombination factor protein RarA | ||
NPJHOEFD_01004 | 4.2e-108 | rarA | L | recombination factor protein RarA | ||
NPJHOEFD_01005 | 5.7e-172 | 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 | |
NPJHOEFD_01006 | 5.6e-55 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
NPJHOEFD_01007 | 1.6e-36 | |||||
NPJHOEFD_01008 | 1.1e-08 | |||||
NPJHOEFD_01009 | 5.6e-61 | Z012_12235 | S | Baseplate J-like protein | ||
NPJHOEFD_01010 | 4.1e-83 | ydcK | S | Belongs to the SprT family | ||
NPJHOEFD_01012 | 3.5e-73 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
NPJHOEFD_01013 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
NPJHOEFD_01014 | 3.3e-29 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NPJHOEFD_01015 | 5.8e-203 | camS | S | sex pheromone | ||
NPJHOEFD_01016 | 1.5e-49 | 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) | |
NPJHOEFD_01017 | 2.9e-268 | 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) | |
NPJHOEFD_01018 | 2.9e-97 | D | VirC1 protein | |||
NPJHOEFD_01020 | 5e-39 | relB | L | RelB antitoxin | ||
NPJHOEFD_01021 | 1.6e-35 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
NPJHOEFD_01022 | 6.6e-87 | bcgIB | 2.1.1.72, 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
NPJHOEFD_01023 | 5.6e-241 | V | N-6 DNA Methylase | |||
NPJHOEFD_01024 | 6e-85 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
NPJHOEFD_01025 | 2.7e-216 | aspC | 2.6.1.1 | E | Aminotransferase | |
NPJHOEFD_01026 | 1.7e-260 | V | ABC-type multidrug transport system, ATPase and permease components | |||
NPJHOEFD_01027 | 1.1e-51 | yifK | E | Amino acid permease | ||
NPJHOEFD_01028 | 6.4e-93 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NPJHOEFD_01029 | 5.6e-214 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
NPJHOEFD_01030 | 2.8e-49 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
NPJHOEFD_01031 | 2.9e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
NPJHOEFD_01033 | 3.8e-216 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
NPJHOEFD_01034 | 3.5e-175 | S | Cysteine-rich secretory protein family | |||
NPJHOEFD_01035 | 1.6e-41 | |||||
NPJHOEFD_01036 | 2.6e-118 | M | NlpC/P60 family | |||
NPJHOEFD_01037 | 1.4e-136 | M | NlpC P60 family protein | |||
NPJHOEFD_01038 | 7.5e-35 | M | NlpC/P60 family | |||
NPJHOEFD_01039 | 2.9e-30 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NPJHOEFD_01040 | 1.4e-31 | O | OsmC-like protein | |||
NPJHOEFD_01042 | 6.7e-173 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NPJHOEFD_01043 | 4.3e-24 | S | SLAP domain | |||
NPJHOEFD_01044 | 3.8e-144 | S | SLAP domain | |||
NPJHOEFD_01045 | 1.5e-217 | natB | CP | ABC-2 family transporter protein | ||
NPJHOEFD_01046 | 1.8e-136 | fruR | K | DeoR C terminal sensor domain | ||
NPJHOEFD_01047 | 2.2e-168 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
NPJHOEFD_01048 | 3.7e-250 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
NPJHOEFD_01049 | 9.2e-95 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
NPJHOEFD_01050 | 2e-105 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
NPJHOEFD_01051 | 4.3e-66 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
NPJHOEFD_01052 | 1.1e-90 | 3.6.3.8 | P | P-type ATPase | ||
NPJHOEFD_01053 | 7.3e-44 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NPJHOEFD_01054 | 6.6e-59 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
NPJHOEFD_01055 | 5.8e-112 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
NPJHOEFD_01056 | 5.2e-59 | S | Iron-sulphur cluster biosynthesis | |||
NPJHOEFD_01057 | 4.4e-135 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
NPJHOEFD_01058 | 8.7e-130 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
NPJHOEFD_01059 | 4.3e-199 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NPJHOEFD_01060 | 1.6e-182 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NPJHOEFD_01061 | 1.2e-241 | S | response to antibiotic | |||
NPJHOEFD_01062 | 4.9e-125 | |||||
NPJHOEFD_01063 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
NPJHOEFD_01064 | 9.8e-23 | 2.7.1.191 | G | PTS system fructose IIA component | ||
NPJHOEFD_01065 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
NPJHOEFD_01066 | 8.5e-154 | spo0J | K | Belongs to the ParB family | ||
NPJHOEFD_01067 | 9.6e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
NPJHOEFD_01068 | 1.7e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NPJHOEFD_01069 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
NPJHOEFD_01070 | 3.1e-21 | S | Protein of unknown function (DUF805) | |||
NPJHOEFD_01072 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
NPJHOEFD_01073 | 1.4e-113 | ecsB | U | ABC transporter | ||
NPJHOEFD_01074 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
NPJHOEFD_01075 | 8.7e-245 | ynbB | 4.4.1.1 | P | aluminum resistance | |
NPJHOEFD_01076 | 4.1e-50 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NPJHOEFD_01077 | 1.4e-217 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NPJHOEFD_01078 | 2.6e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
NPJHOEFD_01079 | 2.4e-286 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
NPJHOEFD_01080 | 1.3e-28 | csaB | M | Glycosyl transferases group 1 | ||
NPJHOEFD_01081 | 9.5e-33 | |||||
NPJHOEFD_01082 | 1.2e-48 | |||||
NPJHOEFD_01083 | 8.6e-11 | |||||
NPJHOEFD_01084 | 1.1e-62 | |||||
NPJHOEFD_01085 | 2.2e-30 | |||||
NPJHOEFD_01086 | 5.7e-205 | pepF | E | oligoendopeptidase F | ||
NPJHOEFD_01087 | 2.9e-90 | msmX | P | Belongs to the ABC transporter superfamily | ||
NPJHOEFD_01088 | 1.3e-213 | malE | G | Bacterial extracellular solute-binding protein | ||
NPJHOEFD_01089 | 1.1e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
NPJHOEFD_01090 | 3.3e-147 | malG | P | ABC transporter permease | ||
NPJHOEFD_01091 | 4.3e-67 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_01094 | 3.1e-27 | |||||
NPJHOEFD_01095 | 2.1e-24 | |||||
NPJHOEFD_01096 | 2.8e-202 | steT | E | amino acid | ||
NPJHOEFD_01097 | 2.4e-26 | steT | E | amino acid | ||
NPJHOEFD_01098 | 8.6e-243 | steT | E | amino acid | ||
NPJHOEFD_01099 | 1.9e-129 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
NPJHOEFD_01100 | 1.9e-147 | glnH | ET | ABC transporter | ||
NPJHOEFD_01101 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
NPJHOEFD_01102 | 6.9e-309 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
NPJHOEFD_01103 | 1.4e-25 | V | ABC transporter transmembrane region | |||
NPJHOEFD_01104 | 1.3e-174 | |||||
NPJHOEFD_01105 | 2.8e-47 | lysM | M | LysM domain | ||
NPJHOEFD_01106 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
NPJHOEFD_01107 | 1.3e-250 | dtpT | U | amino acid peptide transporter | ||
NPJHOEFD_01108 | 1.2e-18 | S | Sugar efflux transporter for intercellular exchange | |||
NPJHOEFD_01109 | 6.6e-70 | XK27_02470 | K | LytTr DNA-binding domain | ||
NPJHOEFD_01110 | 2.1e-92 | liaI | S | membrane | ||
NPJHOEFD_01111 | 4e-16 | |||||
NPJHOEFD_01112 | 3.9e-186 | S | Putative peptidoglycan binding domain | |||
NPJHOEFD_01113 | 1.9e-157 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
NPJHOEFD_01114 | 9e-121 | |||||
NPJHOEFD_01115 | 1.7e-53 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
NPJHOEFD_01116 | 3.7e-207 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
NPJHOEFD_01117 | 4.8e-94 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
NPJHOEFD_01118 | 5.1e-72 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
NPJHOEFD_01119 | 1.9e-118 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
NPJHOEFD_01120 | 1.5e-102 | GM | NmrA-like family | |||
NPJHOEFD_01121 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
NPJHOEFD_01122 | 1.5e-189 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
NPJHOEFD_01123 | 6.7e-127 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NPJHOEFD_01124 | 2.2e-27 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NPJHOEFD_01125 | 2.3e-78 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
NPJHOEFD_01126 | 4.7e-71 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
NPJHOEFD_01127 | 9.5e-83 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
NPJHOEFD_01128 | 6.7e-43 | yhjH | 3.1.4.52 | T | Putative diguanylate phosphodiesterase | |
NPJHOEFD_01129 | 1.1e-130 | D | Alpha beta | |||
NPJHOEFD_01130 | 1e-297 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
NPJHOEFD_01131 | 3.2e-156 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NPJHOEFD_01132 | 6.1e-136 | V | ABC transporter transmembrane region | |||
NPJHOEFD_01133 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
NPJHOEFD_01134 | 3.6e-24 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
NPJHOEFD_01135 | 1.2e-100 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
NPJHOEFD_01136 | 6.3e-39 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NPJHOEFD_01137 | 5.4e-231 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
NPJHOEFD_01138 | 6.8e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
NPJHOEFD_01139 | 1e-128 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
NPJHOEFD_01140 | 3.5e-27 | 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 | ||
NPJHOEFD_01141 | 4.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
NPJHOEFD_01142 | 1.3e-91 | 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 | ||
NPJHOEFD_01143 | 2.2e-12 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
NPJHOEFD_01144 | 1.5e-11 | GT2,GT4 | M | family 8 | ||
NPJHOEFD_01145 | 7e-84 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
NPJHOEFD_01146 | 1.8e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
NPJHOEFD_01147 | 8.7e-140 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
NPJHOEFD_01148 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
NPJHOEFD_01149 | 9e-26 | |||||
NPJHOEFD_01150 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
NPJHOEFD_01151 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NPJHOEFD_01152 | 5.7e-106 | 2.4.1.58 | GT8 | M | family 8 | |
NPJHOEFD_01153 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
NPJHOEFD_01154 | 8.2e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
NPJHOEFD_01155 | 1.6e-108 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
NPJHOEFD_01156 | 4.9e-25 | M | domain protein | |||
NPJHOEFD_01157 | 8e-45 | K | Penicillinase repressor | |||
NPJHOEFD_01158 | 1.6e-118 | |||||
NPJHOEFD_01159 | 2.1e-84 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
NPJHOEFD_01160 | 3.8e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NPJHOEFD_01161 | 1.7e-129 | licT | K | CAT RNA binding domain | ||
NPJHOEFD_01162 | 1.2e-154 | S | hydrolase | |||
NPJHOEFD_01163 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
NPJHOEFD_01164 | 9.1e-175 | rihB | 3.2.2.1 | F | Nucleoside | |
NPJHOEFD_01165 | 5.3e-62 | kup | P | Transport of potassium into the cell | ||
NPJHOEFD_01166 | 4.9e-230 | kup | P | Transport of potassium into the cell | ||
NPJHOEFD_01167 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
NPJHOEFD_01168 | 7.6e-94 | S | VanZ like family | |||
NPJHOEFD_01169 | 3.5e-101 | ylbE | GM | NAD(P)H-binding | ||
NPJHOEFD_01170 | 3.7e-27 | 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 | ||
NPJHOEFD_01171 | 1.9e-53 | L | Transposase and inactivated derivatives | |||
NPJHOEFD_01172 | 3.1e-240 | oppA | E | ABC transporter substrate-binding protein | ||
NPJHOEFD_01173 | 4.1e-133 | cysA | V | ABC transporter, ATP-binding protein | ||
NPJHOEFD_01174 | 3.4e-23 | |||||
NPJHOEFD_01176 | 6e-177 | 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) | |
NPJHOEFD_01177 | 1e-291 | S | SLAP domain | |||
NPJHOEFD_01178 | 5.3e-80 | |||||
NPJHOEFD_01179 | 2.6e-173 | 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 | |
NPJHOEFD_01180 | 1.5e-147 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
NPJHOEFD_01181 | 4.5e-39 | veg | S | Biofilm formation stimulator VEG | ||
NPJHOEFD_01182 | 1.8e-38 | 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 | |
NPJHOEFD_01183 | 4.6e-103 | mdlB | V | ABC transporter | ||
NPJHOEFD_01184 | 8.4e-60 | 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 | |
NPJHOEFD_01185 | 4e-249 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
NPJHOEFD_01186 | 2.8e-134 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
NPJHOEFD_01187 | 7.9e-149 | lctP | C | L-lactate permease | ||
NPJHOEFD_01188 | 6.7e-89 | 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) | |
NPJHOEFD_01189 | 1.5e-216 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
NPJHOEFD_01190 | 2e-11 | |||||
NPJHOEFD_01191 | 8.4e-28 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_01193 | 9.2e-57 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
NPJHOEFD_01194 | 1.8e-44 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
NPJHOEFD_01195 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
NPJHOEFD_01196 | 8.2e-114 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
NPJHOEFD_01197 | 1.2e-105 | |||||
NPJHOEFD_01198 | 6.9e-173 | EGP | Sugar (and other) transporter | |||
NPJHOEFD_01199 | 1.2e-55 | 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 | |
NPJHOEFD_01200 | 9.6e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NPJHOEFD_01201 | 3.1e-09 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
NPJHOEFD_01202 | 3.8e-137 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
NPJHOEFD_01203 | 1.2e-145 | V | ABC transporter, ATP-binding protein | |||
NPJHOEFD_01204 | 4.2e-144 | V | ABC transporter, ATP-binding protein | |||
NPJHOEFD_01206 | 5.3e-41 | |||||
NPJHOEFD_01207 | 1.4e-76 | K | DNA-templated transcription, initiation | |||
NPJHOEFD_01208 | 1.1e-25 | |||||
NPJHOEFD_01209 | 2.2e-103 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NPJHOEFD_01211 | 6.7e-19 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NPJHOEFD_01212 | 7.5e-101 | S | SLAP domain | |||
NPJHOEFD_01213 | 4.3e-40 | S | Protein of unknown function (DUF2922) | |||
NPJHOEFD_01214 | 5.5e-30 | |||||
NPJHOEFD_01216 | 1.4e-60 | 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 | |
NPJHOEFD_01217 | 2.2e-49 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
NPJHOEFD_01218 | 9.2e-61 | fabZ | 3.5.1.108, 4.2.1.59 | I | FabA-like domain | |
NPJHOEFD_01219 | 9.6e-237 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
NPJHOEFD_01220 | 3.3e-139 | 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 | |
NPJHOEFD_01221 | 1.1e-128 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
NPJHOEFD_01222 | 1.9e-122 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
NPJHOEFD_01223 | 1.1e-79 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
NPJHOEFD_01224 | 2.3e-173 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NPJHOEFD_01225 | 8.7e-154 | V | ABC transporter transmembrane region | |||
NPJHOEFD_01226 | 5.6e-40 | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | |||
NPJHOEFD_01227 | 1.2e-46 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
NPJHOEFD_01228 | 6.3e-205 | napA | P | Sodium/hydrogen exchanger family | ||
NPJHOEFD_01229 | 0.0 | cadA | P | P-type ATPase | ||
NPJHOEFD_01230 | 1.5e-80 | ykuL | S | (CBS) domain | ||
NPJHOEFD_01231 | 1e-207 | ywhK | S | Membrane | ||
NPJHOEFD_01232 | 4.1e-44 | |||||
NPJHOEFD_01233 | 1.2e-18 | S | D-Ala-teichoic acid biosynthesis protein | |||
NPJHOEFD_01234 | 2.1e-285 | 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 | |
NPJHOEFD_01235 | 1.9e-236 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
NPJHOEFD_01236 | 1.7e-35 | 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 | |
NPJHOEFD_01237 | 7.3e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
NPJHOEFD_01238 | 7.6e-177 | pbpX2 | V | Beta-lactamase | ||
NPJHOEFD_01239 | 2.3e-133 | S | Protein of unknown function (DUF975) | |||
NPJHOEFD_01240 | 2.7e-137 | lysA2 | M | Glycosyl hydrolases family 25 | ||
NPJHOEFD_01241 | 2.8e-60 | G | Belongs to the glycosyl hydrolase 31 family | |||
NPJHOEFD_01242 | 2.5e-144 | I | alpha/beta hydrolase fold | |||
NPJHOEFD_01243 | 4.9e-129 | yibF | S | overlaps another CDS with the same product name | ||
NPJHOEFD_01244 | 6.3e-202 | yibE | S | overlaps another CDS with the same product name | ||
NPJHOEFD_01245 | 1.6e-26 | ftsL | D | Cell division protein FtsL | ||
NPJHOEFD_01246 | 2.3e-159 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
NPJHOEFD_01247 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
NPJHOEFD_01248 | 4.6e-89 | 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 | ||
NPJHOEFD_01249 | 5.4e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
NPJHOEFD_01250 | 8.4e-140 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
NPJHOEFD_01251 | 1.7e-145 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
NPJHOEFD_01252 | 2.9e-35 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
NPJHOEFD_01253 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NPJHOEFD_01254 | 4.3e-55 | |||||
NPJHOEFD_01255 | 5.8e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
NPJHOEFD_01256 | 2.1e-92 | yutD | S | Protein of unknown function (DUF1027) | ||
NPJHOEFD_01257 | 3.4e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
NPJHOEFD_01258 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
NPJHOEFD_01259 | 6.8e-116 | dedA | S | SNARE-like domain protein | ||
NPJHOEFD_01260 | 7.5e-183 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
NPJHOEFD_01261 | 2e-110 | P | ABC transporter permease | |||
NPJHOEFD_01262 | 9.6e-110 | papP | P | ABC transporter, permease protein | ||
NPJHOEFD_01264 | 8.8e-62 | yodB | K | Transcriptional regulator, HxlR family | ||
NPJHOEFD_01265 | 5e-134 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NPJHOEFD_01266 | 1.9e-158 | endA | F | DNA RNA non-specific endonuclease | ||
NPJHOEFD_01267 | 8e-182 | dnaQ | 2.7.7.7 | L | EXOIII | |
NPJHOEFD_01268 | 9e-158 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
NPJHOEFD_01269 | 3.8e-87 | yviA | S | Protein of unknown function (DUF421) | ||
NPJHOEFD_01270 | 9.2e-21 | comGA | NU | Type II IV secretion system protein | ||
NPJHOEFD_01271 | 1.7e-171 | comGB | NU | type II secretion system | ||
NPJHOEFD_01272 | 3.1e-43 | comGC | U | competence protein ComGC | ||
NPJHOEFD_01273 | 1.8e-69 | |||||
NPJHOEFD_01274 | 2.3e-41 | |||||
NPJHOEFD_01275 | 3.8e-77 | comGF | U | Putative Competence protein ComGF | ||
NPJHOEFD_01276 | 1.6e-21 | |||||
NPJHOEFD_01277 | 1.9e-186 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
NPJHOEFD_01278 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
NPJHOEFD_01279 | 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 | ||
NPJHOEFD_01280 | 1.7e-102 | 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 | |
NPJHOEFD_01281 | 1.5e-186 | 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 | |
NPJHOEFD_01282 | 9.6e-41 | yajC | U | Preprotein translocase | ||
NPJHOEFD_01283 | 9.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
NPJHOEFD_01284 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
NPJHOEFD_01285 | 5.9e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
NPJHOEFD_01286 | 1.9e-22 | K | Putative DNA-binding domain | |||
NPJHOEFD_01287 | 2.2e-238 | pyrP | F | Permease | ||
NPJHOEFD_01288 | 8.8e-90 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NPJHOEFD_01289 | 2.9e-12 | |||||
NPJHOEFD_01290 | 2e-18 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
NPJHOEFD_01291 | 1.7e-29 | M | Protein of unknown function (DUF3737) | |||
NPJHOEFD_01292 | 3.6e-51 | L | Belongs to the 'phage' integrase family | |||
NPJHOEFD_01293 | 3.9e-246 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
NPJHOEFD_01294 | 3.3e-176 | hrtB | V | ABC transporter permease | ||
NPJHOEFD_01295 | 3.2e-92 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
NPJHOEFD_01296 | 3.5e-111 | G | phosphoglycerate mutase | |||
NPJHOEFD_01297 | 1.3e-115 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NPJHOEFD_01298 | 6.6e-119 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
NPJHOEFD_01299 | 2.6e-89 | G | Histidine phosphatase superfamily (branch 1) | |||
NPJHOEFD_01300 | 1.2e-105 | G | Phosphoglycerate mutase family | |||
NPJHOEFD_01301 | 4.7e-159 | D | nuclear chromosome segregation | |||
NPJHOEFD_01302 | 5.8e-78 | M | LysM domain protein | |||
NPJHOEFD_01304 | 1e-44 | S | PFAM Archaeal ATPase | |||
NPJHOEFD_01305 | 6.8e-181 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NPJHOEFD_01306 | 2.9e-23 | yxeH | S | hydrolase | ||
NPJHOEFD_01307 | 3.1e-16 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
NPJHOEFD_01308 | 1.8e-48 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | ||
NPJHOEFD_01309 | 2.6e-23 | 1.1.1.100 | S | KR domain | ||
NPJHOEFD_01310 | 6.4e-16 | ymfI | 1.1.1.100, 1.3.1.28 | S | oxidoreductase activity | |
NPJHOEFD_01312 | 1.9e-83 | K | Transcriptional regulator | |||
NPJHOEFD_01313 | 6.1e-61 | K | Transcriptional regulator | |||
NPJHOEFD_01314 | 2e-225 | S | cog cog1373 | |||
NPJHOEFD_01315 | 9.7e-146 | S | haloacid dehalogenase-like hydrolase | |||
NPJHOEFD_01316 | 3.3e-140 | repB | EP | Plasmid replication protein | ||
NPJHOEFD_01317 | 1e-33 | S | helix_turn_helix, Deoxyribose operon repressor | |||
NPJHOEFD_01318 | 4.1e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
NPJHOEFD_01319 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
NPJHOEFD_01320 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
NPJHOEFD_01321 | 2e-267 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
NPJHOEFD_01322 | 5.3e-11 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
NPJHOEFD_01323 | 2.7e-67 | treR | K | UTRA | ||
NPJHOEFD_01324 | 2.2e-21 | treR | K | UTRA | ||
NPJHOEFD_01325 | 1.7e-51 | blpT | ||||
NPJHOEFD_01327 | 4.7e-117 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
NPJHOEFD_01328 | 1.4e-152 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
NPJHOEFD_01329 | 6.4e-240 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NPJHOEFD_01330 | 3e-60 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
NPJHOEFD_01331 | 2.4e-36 | |||||
NPJHOEFD_01334 | 1.8e-31 | |||||
NPJHOEFD_01335 | 6.5e-114 | |||||
NPJHOEFD_01336 | 4.6e-268 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
NPJHOEFD_01337 | 8.1e-112 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NPJHOEFD_01338 | 3e-184 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
NPJHOEFD_01339 | 5.8e-73 | S | domain protein | |||
NPJHOEFD_01341 | 5.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
NPJHOEFD_01342 | 1.3e-15 | topA2 | 5.99.1.2 | G | Topoisomerase IA | |
NPJHOEFD_01343 | 1.8e-43 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
NPJHOEFD_01344 | 2.2e-90 | 2.7.7.65 | T | GGDEF domain | ||
NPJHOEFD_01345 | 8.2e-36 | |||||
NPJHOEFD_01346 | 4.2e-56 | 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 | ||
NPJHOEFD_01347 | 3e-63 | 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 | ||
NPJHOEFD_01348 | 1.1e-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 | |
NPJHOEFD_01349 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
NPJHOEFD_01350 | 1.4e-153 | ecfA1 | P | ATP-binding (A) component of a common 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 | ||
NPJHOEFD_01351 | 3.5e-157 | ecfA | 3.6.3.55 | P | ATP-binding (A) component of a common 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 | |
NPJHOEFD_01352 | 1.8e-81 | M | NlpC/P60 family | |||
NPJHOEFD_01353 | 2.1e-131 | cobQ | S | glutamine amidotransferase | ||
NPJHOEFD_01354 | 5.1e-70 | yeaL | S | Protein of unknown function (DUF441) | ||
NPJHOEFD_01355 | 3.5e-21 | |||||
NPJHOEFD_01356 | 1.1e-104 | cbiQ | P | cobalt transport | ||
NPJHOEFD_01357 | 2.3e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NPJHOEFD_01358 | 1.6e-235 | S | Peptidase M16 | |||
NPJHOEFD_01359 | 6.7e-122 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
NPJHOEFD_01360 | 7e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
NPJHOEFD_01361 | 7.7e-162 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
NPJHOEFD_01362 | 1e-165 | 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 | |
NPJHOEFD_01363 | 1e-125 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
NPJHOEFD_01367 | 3.4e-52 | S | COG0790 FOG TPR repeat, SEL1 subfamily | |||
NPJHOEFD_01368 | 1.7e-39 | L | Protein of unknown function (DUF3991) | |||
NPJHOEFD_01369 | 4.6e-111 | S | Fic/DOC family | |||
NPJHOEFD_01370 | 1.5e-47 | L | Psort location Cytoplasmic, score | |||
NPJHOEFD_01371 | 2.2e-23 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
NPJHOEFD_01372 | 9.6e-18 | S | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
NPJHOEFD_01373 | 6.8e-214 | 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) | |
NPJHOEFD_01374 | 1.3e-18 | 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) | |
NPJHOEFD_01375 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
NPJHOEFD_01376 | 1.4e-110 | yjbF | S | SNARE associated Golgi protein | ||
NPJHOEFD_01377 | 6e-151 | I | alpha/beta hydrolase fold | |||
NPJHOEFD_01378 | 1.2e-62 | hipB | K | Helix-turn-helix | ||
NPJHOEFD_01379 | 1.1e-104 | vanZ | V | VanZ like family | ||
NPJHOEFD_01380 | 2.7e-189 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
NPJHOEFD_01381 | 9.3e-86 | 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 | |
NPJHOEFD_01382 | 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 | |
NPJHOEFD_01383 | 1.1e-209 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
NPJHOEFD_01384 | 2.6e-35 | yaaA | S | S4 domain protein YaaA | ||
NPJHOEFD_01385 | 3.8e-199 | 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 | |
NPJHOEFD_01386 | 4.7e-182 | pepA | E | M42 glutamyl aminopeptidase | ||
NPJHOEFD_01387 | 2.2e-311 | ybiT | S | ABC transporter, ATP-binding protein | ||
NPJHOEFD_01388 | 5.9e-174 | S | Aldo keto reductase | |||
NPJHOEFD_01389 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
NPJHOEFD_01390 | 1.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
NPJHOEFD_01391 | 8.9e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
NPJHOEFD_01392 | 2.8e-154 | holB | 2.7.7.7 | L | DNA polymerase III | |
NPJHOEFD_01393 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
NPJHOEFD_01394 | 5.1e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
NPJHOEFD_01395 | 1.4e-130 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
NPJHOEFD_01396 | 2.2e-85 | S | ECF transporter, substrate-specific component | |||
NPJHOEFD_01397 | 2.4e-133 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
NPJHOEFD_01398 | 1.1e-86 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
NPJHOEFD_01399 | 5.8e-84 | tsaD | 2.3.1.234 | J | 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 | |
NPJHOEFD_01400 | 2.7e-76 | tsaD | 2.3.1.234 | J | 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 | |
NPJHOEFD_01401 | 1e-88 | L | Transposase IS66 family | |||
NPJHOEFD_01402 | 1.7e-40 | recN | L | May be involved in recombinational repair of damaged DNA | ||
NPJHOEFD_01403 | 8.1e-151 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
NPJHOEFD_01404 | 1e-159 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NPJHOEFD_01405 | 5.8e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
NPJHOEFD_01406 | 3.6e-34 | S | Phage derived protein Gp49-like (DUF891) | |||
NPJHOEFD_01407 | 7.1e-35 | K | Helix-turn-helix XRE-family like proteins | |||
NPJHOEFD_01408 | 1.1e-188 | L | N-6 DNA Methylase | |||
NPJHOEFD_01409 | 2.2e-26 | S | Type I restriction modification DNA specificity domain | |||
NPJHOEFD_01410 | 2.4e-51 | S | Domain of unknown function DUF1829 | |||
NPJHOEFD_01411 | 2.9e-23 | |||||
NPJHOEFD_01412 | 2.7e-134 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NPJHOEFD_01413 | 1.3e-176 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
NPJHOEFD_01414 | 3.7e-36 | |||||
NPJHOEFD_01415 | 2.3e-38 | C | FMN_bind | |||
NPJHOEFD_01416 | 2.3e-56 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
NPJHOEFD_01417 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
NPJHOEFD_01418 | 7.1e-98 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
NPJHOEFD_01419 | 5.4e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NPJHOEFD_01420 | 1.6e-147 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NPJHOEFD_01421 | 1.6e-117 | fhuC | P | ABC transporter | ||
NPJHOEFD_01422 | 5e-129 | znuB | U | ABC 3 transport family | ||
NPJHOEFD_01423 | 1e-92 | S | PFAM Archaeal ATPase | |||
NPJHOEFD_01424 | 4.5e-192 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
NPJHOEFD_01425 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
NPJHOEFD_01426 | 8.9e-132 | |||||
NPJHOEFD_01427 | 4.6e-160 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
NPJHOEFD_01428 | 2.3e-30 | |||||
NPJHOEFD_01429 | 2.4e-121 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
NPJHOEFD_01430 | 5.5e-35 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
NPJHOEFD_01431 | 6.2e-12 | |||||
NPJHOEFD_01432 | 1.5e-16 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NPJHOEFD_01433 | 4.1e-78 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
NPJHOEFD_01435 | 1.3e-212 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
NPJHOEFD_01436 | 1.8e-119 | S | Putative esterase | |||
NPJHOEFD_01437 | 5.1e-66 | clcA | P | chloride | ||
NPJHOEFD_01438 | 4e-32 | E | Zn peptidase | |||
NPJHOEFD_01439 | 3.7e-58 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
NPJHOEFD_01440 | 1.2e-44 | |||||
NPJHOEFD_01441 | 8.4e-55 | S | Bacteriocin helveticin-J | |||
NPJHOEFD_01442 | 2.8e-42 | S | Bacteriocin helveticin-J |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)