| 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 |
Showing 1 to 100 of 1,332 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)