| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| HGHAFENF_00001 | 7.7e-107 | mltD | CBM50 | M | NlpC P60 family protein | |
| HGHAFENF_00002 | 8.3e-195 | L | PFAM transposase, IS204 IS1001 IS1096 IS1165 family protein | |||
| HGHAFENF_00003 | 3.7e-28 | |||||
| HGHAFENF_00004 | 1.7e-187 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| HGHAFENF_00005 | 0.0 | rnjA | 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 | ||
| HGHAFENF_00006 | 3.1e-33 | ykzG | S | Belongs to the UPF0356 family | ||
| HGHAFENF_00007 | 1.6e-85 | |||||
| HGHAFENF_00008 | 1.2e-100 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
| HGHAFENF_00009 | 1.6e-210 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
| HGHAFENF_00010 | 4.5e-180 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
| HGHAFENF_00011 | 1.8e-208 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
| HGHAFENF_00012 | 2.6e-266 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
| HGHAFENF_00013 | 1.4e-162 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
| HGHAFENF_00014 | 3.6e-45 | yktA | S | Belongs to the UPF0223 family | ||
| HGHAFENF_00015 | 7e-136 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
| HGHAFENF_00016 | 0.0 | typA | T | GTP-binding protein TypA | ||
| HGHAFENF_00017 | 6e-120 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
| HGHAFENF_00018 | 1.3e-260 | |||||
| HGHAFENF_00019 | 1.6e-205 | ftsW | D | Belongs to the SEDS family | ||
| HGHAFENF_00020 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
| HGHAFENF_00021 | 1.5e-49 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
| HGHAFENF_00022 | 1.7e-102 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
| HGHAFENF_00023 | 2.1e-85 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
| HGHAFENF_00024 | 9.6e-197 | ylbL | T | Belongs to the peptidase S16 family | ||
| HGHAFENF_00025 | 1.2e-121 | comEA | L | Competence protein ComEA | ||
| HGHAFENF_00026 | 6.4e-79 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
| HGHAFENF_00027 | 0.0 | comEC | S | Competence protein ComEC | ||
| HGHAFENF_00028 | 4.1e-187 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
| HGHAFENF_00029 | 1.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
| HGHAFENF_00030 | 6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
| HGHAFENF_00031 | 6.3e-192 | mdtG | EGP | Major Facilitator Superfamily | ||
| HGHAFENF_00032 | 6.2e-157 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
| HGHAFENF_00033 | 0.0 | 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 | ||
| HGHAFENF_00034 | 1.1e-159 | S | Tetratricopeptide repeat | |||
| HGHAFENF_00035 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
| HGHAFENF_00036 | 4.1e-213 | 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 | ||
| HGHAFENF_00037 | 3.3e-236 | 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 | ||
| HGHAFENF_00038 | 5.1e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
| HGHAFENF_00039 | 2.2e-49 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
| HGHAFENF_00040 | 9.9e-73 | S | Iron-sulphur cluster biosynthesis | |||
| HGHAFENF_00041 | 4.3e-22 | |||||
| HGHAFENF_00042 | 9.2e-270 | glnPH2 | P | ABC transporter permease | ||
| HGHAFENF_00043 | 1.3e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
| HGHAFENF_00044 | 0.0 | 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 | ||
| HGHAFENF_00045 | 2.9e-126 | epsB | M | biosynthesis protein | ||
| HGHAFENF_00046 | 7.3e-124 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
| HGHAFENF_00047 | 3.5e-146 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
| HGHAFENF_00048 | 9.6e-180 | cps4D | 5.1.3.2 | M | RmlD substrate binding domain | |
| HGHAFENF_00049 | 1.8e-127 | tuaA | M | Bacterial sugar transferase | ||
| HGHAFENF_00050 | 1.2e-202 | cps4F | 2.4.1.21, 2.4.1.306 | GT4,GT5 | M | Glycosyl transferases group 1 |
| HGHAFENF_00051 | 1.1e-184 | cps4G | M | Glycosyltransferase Family 4 | ||
| HGHAFENF_00052 | 5.6e-231 | |||||
| HGHAFENF_00053 | 4.3e-175 | cps4I | M | Glycosyltransferase like family 2 | ||
| HGHAFENF_00054 | 1.4e-262 | cps4J | S | Polysaccharide biosynthesis protein | ||
| HGHAFENF_00055 | 5.4e-253 | cpdA | S | Calcineurin-like phosphoesterase | ||
| HGHAFENF_00056 | 6.7e-292 | fruA | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GT | Phosphotransferase System | |
| HGHAFENF_00057 | 5.1e-170 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
| HGHAFENF_00058 | 1.5e-135 | fruR | K | DeoR C terminal sensor domain | ||
| HGHAFENF_00059 | 2.4e-245 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
| HGHAFENF_00060 | 3.2e-46 | |||||
| HGHAFENF_00061 | 2.8e-179 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
| HGHAFENF_00062 | 5.6e-141 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
| HGHAFENF_00063 | 2e-50 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
| HGHAFENF_00064 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
| HGHAFENF_00065 | 2.9e-93 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
| HGHAFENF_00066 | 1.5e-103 | K | Helix-turn-helix domain | |||
| HGHAFENF_00067 | 7.2e-212 | EGP | Major facilitator Superfamily | |||
| HGHAFENF_00068 | 8.5e-57 | ybjQ | S | Belongs to the UPF0145 family | ||
| HGHAFENF_00069 | 2.1e-140 | Q | Methyltransferase | |||
| HGHAFENF_00070 | 1.6e-31 | |||||
| HGHAFENF_00073 | 4e-50 | L | Belongs to the 'phage' integrase family | |||
| HGHAFENF_00075 | 4.9e-43 | L | HTH-like domain | |||
| HGHAFENF_00077 | 2.7e-26 | S | Short C-terminal domain | |||
| HGHAFENF_00078 | 1.9e-17 | S | Short C-terminal domain | |||
| HGHAFENF_00081 | 3.4e-177 | csbB | 2.4.1.83 | GT2 | M | Glycosyltransferase like family 2 |
| HGHAFENF_00082 | 3.5e-67 | |||||
| HGHAFENF_00083 | 1.1e-76 | |||||
| HGHAFENF_00084 | 1.3e-215 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
| HGHAFENF_00085 | 3.2e-86 | |||||
| HGHAFENF_00086 | 5.6e-115 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
| HGHAFENF_00087 | 2.9e-36 | ynzC | S | UPF0291 protein | ||
| HGHAFENF_00088 | 4.3e-33 | yneF | S | Uncharacterised protein family (UPF0154) | ||
| HGHAFENF_00089 | 1.2e-117 | plsC | 2.3.1.51 | I | Acyltransferase | |
| HGHAFENF_00090 | 4.2e-133 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
| HGHAFENF_00091 | 2e-49 | yazA | L | GIY-YIG catalytic domain protein | ||
| HGHAFENF_00092 | 2.3e-187 | ldhA | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
| HGHAFENF_00093 | 4.7e-134 | S | Haloacid dehalogenase-like hydrolase | |||
| HGHAFENF_00094 | 6.5e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
| HGHAFENF_00095 | 3.9e-151 | 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 | ||
| HGHAFENF_00096 | 2.2e-128 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
| HGHAFENF_00097 | 2.5e-82 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
| HGHAFENF_00098 | 1.8e-147 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
| HGHAFENF_00099 | 8.4e-137 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
| HGHAFENF_00100 | 9.5e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
| HGHAFENF_00101 | 0.0 | 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 | |
| HGHAFENF_00102 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
| HGHAFENF_00103 | 4.2e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
| HGHAFENF_00104 | 3.3e-217 | nusA | K | Participates in both transcription termination and antitermination | ||
| HGHAFENF_00105 | 9.5e-49 | ylxR | K | Protein of unknown function (DUF448) | ||
| HGHAFENF_00106 | 1.1e-47 | ylxQ | J | ribosomal protein |
Showing 1 to 100 of 2,778 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)