ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
HHLLMEFB_00001 | 3.2e-214 | arcT | 2.6.1.1 | E | Aminotransferase | |
HHLLMEFB_00002 | 1.3e-76 | argR | K | Regulates arginine biosynthesis genes | ||
HHLLMEFB_00003 | 2.5e-11 | |||||
HHLLMEFB_00004 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
HHLLMEFB_00005 | 1e-54 | yheA | S | Belongs to the UPF0342 family | ||
HHLLMEFB_00006 | 4.1e-231 | yhaO | L | Ser Thr phosphatase family protein | ||
HHLLMEFB_00007 | 0.0 | L | AAA domain | |||
HHLLMEFB_00008 | 3.2e-186 | yhaM | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
HHLLMEFB_00009 | 3.3e-214 | |||||
HHLLMEFB_00010 | 3.6e-182 | 3.4.21.102 | M | Peptidase family S41 | ||
HHLLMEFB_00011 | 4.5e-177 | K | LysR substrate binding domain | |||
HHLLMEFB_00012 | 2.1e-111 | 1.3.5.4 | S | NADPH-dependent FMN reductase | ||
HHLLMEFB_00013 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
HHLLMEFB_00014 | 1.7e-99 | |||||
HHLLMEFB_00015 | 3.5e-76 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
HHLLMEFB_00016 | 8.4e-60 | M | domain protein | |||
HHLLMEFB_00017 | 1.2e-22 | M | domain protein | |||
HHLLMEFB_00018 | 1.4e-72 | M | domain protein | |||
HHLLMEFB_00019 | 5.7e-23 | M | domain protein | |||
HHLLMEFB_00021 | 3.9e-213 | ltrA_1 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | ||
HHLLMEFB_00022 | 0.0 | 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | ||
HHLLMEFB_00023 | 7.4e-199 | 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 | |
HHLLMEFB_00024 | 7.9e-272 | mutS | L | ATPase domain of DNA mismatch repair MUTS family | ||
HHLLMEFB_00025 | 7.3e-228 | mutS | L | MutS domain V | ||
HHLLMEFB_00026 | 6.1e-185 | ykoT | GT2 | M | Glycosyl transferase family 2 | |
HHLLMEFB_00027 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
HHLLMEFB_00028 | 1.7e-19 | S | NUDIX domain | |||
HHLLMEFB_00029 | 0.0 | S | membrane | |||
HHLLMEFB_00030 | 1.7e-143 | 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 | |
HHLLMEFB_00031 | 1.8e-86 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
HHLLMEFB_00032 | 6.9e-223 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
HHLLMEFB_00033 | 1.4e-81 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
HHLLMEFB_00034 | 9.3e-106 | GBS0088 | S | Nucleotidyltransferase | ||
HHLLMEFB_00035 | 1.4e-106 | |||||
HHLLMEFB_00036 | 5.1e-116 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
HHLLMEFB_00037 | 3.5e-93 | K | Bacterial regulatory proteins, tetR family | |||
HHLLMEFB_00038 | 5.2e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
HHLLMEFB_00039 | 0.0 | |||||
HHLLMEFB_00040 | 3.5e-61 | |||||
HHLLMEFB_00041 | 1.4e-192 | S | Fn3-like domain | |||
HHLLMEFB_00042 | 2e-102 | S | WxL domain surface cell wall-binding | |||
HHLLMEFB_00043 | 3.5e-78 | S | WxL domain surface cell wall-binding | |||
HHLLMEFB_00044 | 2.5e-119 | draG | 3.2.2.24 | O | ADP-ribosylglycohydrolase | |
HHLLMEFB_00045 | 3.3e-129 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
HHLLMEFB_00046 | 2e-42 | |||||
HHLLMEFB_00047 | 9.9e-82 | hit | FG | histidine triad | ||
HHLLMEFB_00048 | 1.6e-134 | ecsA | V | ABC transporter, ATP-binding protein | ||
HHLLMEFB_00049 | 2.1e-224 | ecsB | U | ABC transporter | ||
HHLLMEFB_00050 | 3.2e-152 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
HHLLMEFB_00051 | 9e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
HHLLMEFB_00052 | 1.6e-54 | ytzB | S | Peptidase propeptide and YPEB domain | ||
HHLLMEFB_00053 | 5.3e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
HHLLMEFB_00054 | 0.0 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
HHLLMEFB_00055 | 1.1e-253 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
HHLLMEFB_00056 | 7.9e-21 | S | Virus attachment protein p12 family | |||
HHLLMEFB_00057 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
HHLLMEFB_00058 | 1.3e-34 | feoA | P | FeoA domain | ||
HHLLMEFB_00059 | 4.2e-144 | sufC | O | FeS assembly ATPase SufC | ||
HHLLMEFB_00060 | 2.6e-244 | sufD | O | FeS assembly protein SufD | ||
HHLLMEFB_00061 | 8e-235 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
HHLLMEFB_00062 | 7.1e-83 | nifU | C | SUF system FeS assembly protein, NifU family | ||
HHLLMEFB_00063 | 1.4e-272 | sufB | O | assembly protein SufB | ||
HHLLMEFB_00064 | 5.5e-45 | yitW | S | Iron-sulfur cluster assembly protein | ||
HHLLMEFB_00065 | 3.1e-111 | hipB | K | Helix-turn-helix | ||
HHLLMEFB_00066 | 4.5e-121 | ybhL | S | Belongs to the BI1 family | ||
HHLLMEFB_00067 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
HHLLMEFB_00068 | 1.5e-157 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
HHLLMEFB_00069 | 2.7e-103 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
HHLLMEFB_00070 | 4.6e-91 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
HHLLMEFB_00071 | 2.2e-244 | dnaB | L | replication initiation and membrane attachment | ||
HHLLMEFB_00072 | 1.1e-170 | dnaI | L | Primosomal protein DnaI | ||
HHLLMEFB_00073 | 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) | |
HHLLMEFB_00074 | 1.8e-84 | 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 | ||
HHLLMEFB_00075 | 1.9e-26 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
HHLLMEFB_00076 | 7.3e-56 | 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 | ||
HHLLMEFB_00077 | 1.1e-55 | |||||
HHLLMEFB_00078 | 5e-240 | yrvN | L | AAA C-terminal domain | ||
HHLLMEFB_00079 | 1.6e-196 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
HHLLMEFB_00080 | 1e-62 | hxlR | K | Transcriptional regulator, HxlR family | ||
HHLLMEFB_00081 | 1.5e-135 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
HHLLMEFB_00082 | 1e-248 | pgaC | GT2 | M | Glycosyl transferase | |
HHLLMEFB_00083 | 3.7e-79 | |||||
HHLLMEFB_00084 | 1.4e-98 | yqeG | S | HAD phosphatase, family IIIA | ||
HHLLMEFB_00085 | 4.5e-216 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
HHLLMEFB_00086 | 1.1e-50 | yhbY | J | RNA-binding protein | ||
HHLLMEFB_00087 | 1.4e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
HHLLMEFB_00088 | 3.2e-115 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
HHLLMEFB_00089 | 2.1e-58 | 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 | ||
HHLLMEFB_00090 | 5.8e-140 | yqeM | Q | Methyltransferase | ||
HHLLMEFB_00091 | 1.7e-218 | ylbM | S | Belongs to the UPF0348 family | ||
HHLLMEFB_00092 | 1.6e-97 | yceD | S | Uncharacterized ACR, COG1399 | ||
HHLLMEFB_00093 | 1.4e-88 | S | Peptidase propeptide and YPEB domain | |||
HHLLMEFB_00094 | 1.1e-167 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
HHLLMEFB_00095 | 3.9e-273 | 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 | |
HHLLMEFB_00096 | 1.6e-244 | rarA | L | recombination factor protein RarA | ||
HHLLMEFB_00097 | 4.3e-121 | K | response regulator | |||
HHLLMEFB_00098 | 8e-307 | arlS | 2.7.13.3 | T | Histidine kinase | |
HHLLMEFB_00099 | 3.8e-171 | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | ||
HHLLMEFB_00100 | 0.0 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
HHLLMEFB_00101 | 5e-226 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)