| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| OHAAHJII_00001 | 1e-254 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
| OHAAHJII_00002 | 7.2e-198 | 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 | |
| OHAAHJII_00003 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
| OHAAHJII_00004 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
| OHAAHJII_00005 | 2e-103 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
| OHAAHJII_00006 | 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 | ||
| OHAAHJII_00007 | 6.3e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
| OHAAHJII_00008 | 3e-60 | divIC | D | Septum formation initiator | ||
| OHAAHJII_00010 | 4.5e-236 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
| OHAAHJII_00011 | 1.1e-236 | tilS | 2.4.2.8, 6.3.4.19 | D | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
| OHAAHJII_00012 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
| OHAAHJII_00013 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
| OHAAHJII_00026 | 2.6e-10 | |||||
| OHAAHJII_00032 | 9.2e-110 | mreC | M | Involved in formation and maintenance of cell shape | ||
| OHAAHJII_00033 | 4.2e-84 | mreD | M | rod shape-determining protein MreD | ||
| OHAAHJII_00034 | 2.2e-87 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
| OHAAHJII_00035 | 9.5e-175 | 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) | |
| OHAAHJII_00036 | 4.2e-217 | araT | 2.6.1.1 | E | Aminotransferase | |
| OHAAHJII_00037 | 4.7e-140 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
| OHAAHJII_00038 | 3.6e-180 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
| OHAAHJII_00039 | 4.8e-30 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
| OHAAHJII_00040 | 2.6e-129 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
| OHAAHJII_00041 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
| OHAAHJII_00042 | 2.4e-275 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
| OHAAHJII_00043 | 1.4e-189 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
| OHAAHJII_00044 | 6.8e-101 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
| OHAAHJII_00045 | 2.8e-293 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
| OHAAHJII_00046 | 6.6e-156 | S | CHAP domain | |||
| OHAAHJII_00047 | 1.4e-239 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
| OHAAHJII_00048 | 2.2e-79 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
| OHAAHJII_00049 | 2.3e-201 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
| OHAAHJII_00050 | 1.3e-139 | 1.1.1.169 | H | Ketopantoate reductase | ||
| OHAAHJII_00051 | 6.6e-34 | |||||
| OHAAHJII_00052 | 9.6e-135 | J | Domain of unknown function (DUF4041) | |||
| OHAAHJII_00053 | 2.5e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
| OHAAHJII_00054 | 0.0 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
| OHAAHJII_00055 | 3.1e-69 | argR | K | Regulates arginine biosynthesis genes | ||
| OHAAHJII_00056 | 3.3e-56 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
| OHAAHJII_00057 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
| OHAAHJII_00058 | 1.2e-79 | S | Protein of unknown function (DUF3021) | |||
| OHAAHJII_00059 | 5.3e-72 | K | LytTr DNA-binding domain | |||
| OHAAHJII_00061 | 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 | ||
| OHAAHJII_00063 | 5.9e-103 | 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 | |
| OHAAHJII_00064 | 2.2e-107 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
| OHAAHJII_00065 | 1.5e-231 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
| OHAAHJII_00066 | 6.1e-205 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
| OHAAHJII_00067 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
| OHAAHJII_00073 | 2.6e-10 | |||||
| OHAAHJII_00081 | 5e-199 | L | Belongs to the 'phage' integrase family | |||
| OHAAHJII_00082 | 3.5e-28 | S | Domain of unknown function (DUF3173) | |||
| OHAAHJII_00083 | 2e-67 | |||||
| OHAAHJII_00084 | 1.7e-226 | L | Replication initiation factor | |||
| OHAAHJII_00085 | 6.7e-73 | |||||
| OHAAHJII_00086 | 2.4e-75 | K | transcriptional | |||
| OHAAHJII_00087 | 8.4e-108 | S | Tetratricopeptide repeat | |||
| OHAAHJII_00089 | 2.3e-158 | |||||
| OHAAHJII_00091 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
| OHAAHJII_00092 | 3e-237 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
| OHAAHJII_00093 | 5.5e-36 | XK27_02060 | S | Transglycosylase associated protein | ||
| OHAAHJII_00094 | 3.9e-72 | badR | K | Transcriptional regulator, marr family | ||
| OHAAHJII_00095 | 3.2e-95 | S | reductase | |||
| OHAAHJII_00097 | 2.3e-287 | ahpF | O | alkyl hydroperoxide reductase | ||
| OHAAHJII_00098 | 1.1e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
| OHAAHJII_00099 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
| OHAAHJII_00100 | 1e-182 | 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 | ||
| OHAAHJII_00101 | 1.2e-82 | S | Putative small multi-drug export protein | |||
| OHAAHJII_00102 | 4.8e-76 | ctsR | K | Belongs to the CtsR family | ||
| OHAAHJII_00103 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
| OHAAHJII_00104 | 4.5e-233 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
| OHAAHJII_00105 | 1.1e-228 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
| OHAAHJII_00106 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
| OHAAHJII_00107 | 1e-139 | S | SseB protein N-terminal domain | |||
| OHAAHJII_00108 | 3.3e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
| OHAAHJII_00110 | 8.1e-257 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
| OHAAHJII_00111 | 2.7e-67 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
| OHAAHJII_00113 | 9.7e-135 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
| OHAAHJII_00114 | 2.7e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
| OHAAHJII_00115 | 4.1e-153 | degV | S | DegV family | ||
| OHAAHJII_00117 | 5.1e-22 | K | Transcriptional | |||
| OHAAHJII_00118 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
| OHAAHJII_00119 | 7.3e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
| OHAAHJII_00120 | 1.7e-89 | S | Protein conserved in bacteria | |||
| OHAAHJII_00121 | 6.7e-89 | H | Methyltransferase | |||
| OHAAHJII_00123 | 7.6e-101 | cadD | P | Cadmium resistance transporter | ||
| OHAAHJII_00124 | 4.5e-55 | cadX | K | transcriptional regulator, ArsR family | ||
| OHAAHJII_00125 | 1.6e-11 | |||||
| OHAAHJII_00126 | 1.3e-54 | yiiE | S | protein homotetramerization | ||
| OHAAHJII_00127 | 2.6e-18 | |||||
| OHAAHJII_00128 | 1.5e-29 | K | Helix-turn-helix domain | |||
| OHAAHJII_00129 | 6e-85 | |||||
| OHAAHJII_00130 | 8.5e-140 | srtB | 3.4.22.70 | S | sortase, SrtB family | |
| OHAAHJII_00131 | 2.5e-233 | capA | M | Bacterial capsule synthesis protein | ||
| OHAAHJII_00132 | 1e-38 | gcvR | T | UPF0237 protein | ||
| OHAAHJII_00133 | 2.3e-243 | XK27_08635 | S | UPF0210 protein | ||
| OHAAHJII_00134 | 5.6e-132 | ais | G | Phosphoglycerate mutase | ||
| OHAAHJII_00135 | 6.7e-142 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
| OHAAHJII_00136 | 1.2e-100 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
| OHAAHJII_00137 | 4.1e-184 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
| OHAAHJII_00138 | 8.2e-64 | 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 | ||
| OHAAHJII_00139 | 1.7e-302 | dnaK | O | Heat shock 70 kDa protein |
Showing 1 to 100 of 1,846 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)