ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
GFPNIMHD_00001 | 2.2e-165 | L | Transposase | |||
GFPNIMHD_00002 | 4.8e-274 | yjeM | E | Amino Acid | ||
GFPNIMHD_00003 | 3.4e-280 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
GFPNIMHD_00004 | 1.4e-186 | 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 | |
GFPNIMHD_00005 | 6.4e-90 | 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 | |
GFPNIMHD_00006 | 2.5e-13 | G | Major Facilitator | |||
GFPNIMHD_00007 | 4.2e-228 | G | Major Facilitator | |||
GFPNIMHD_00008 | 0.0 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
GFPNIMHD_00009 | 9e-153 | lysR5 | K | LysR substrate binding domain | ||
GFPNIMHD_00011 | 1.5e-101 | 3.6.1.27 | I | Acid phosphatase homologues | ||
GFPNIMHD_00012 | 6.2e-246 | 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 | |
GFPNIMHD_00013 | 3.7e-18 | S | Sugar efflux transporter for intercellular exchange | |||
GFPNIMHD_00014 | 8.7e-306 | ybiT | S | ABC transporter, ATP-binding protein | ||
GFPNIMHD_00015 | 2.6e-180 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
GFPNIMHD_00016 | 8.9e-227 | pbuG | S | permease | ||
GFPNIMHD_00017 | 6.4e-45 | I | bis(5'-adenosyl)-triphosphatase activity | |||
GFPNIMHD_00018 | 1.2e-231 | pbuG | S | permease | ||
GFPNIMHD_00019 | 3e-45 | K | helix_turn_helix, mercury resistance | |||
GFPNIMHD_00020 | 5.1e-69 | K | helix_turn_helix, mercury resistance | |||
GFPNIMHD_00021 | 3e-232 | pbuG | S | permease | ||
GFPNIMHD_00022 | 8.9e-234 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
GFPNIMHD_00023 | 2.4e-124 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
GFPNIMHD_00024 | 2.5e-118 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
GFPNIMHD_00025 | 5.1e-133 | 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 | |
GFPNIMHD_00026 | 3.2e-158 | yeaE | S | Aldo/keto reductase family | ||
GFPNIMHD_00027 | 6.2e-129 | S | membrane transporter protein | |||
GFPNIMHD_00028 | 1.2e-131 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
GFPNIMHD_00029 | 1.8e-96 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
GFPNIMHD_00030 | 1.9e-160 | ykfB | 5.1.1.20 | M | Belongs to the mandelate racemase muconate lactonizing enzyme family | |
GFPNIMHD_00031 | 9.7e-85 | blaA6 | V | Beta-lactamase | ||
GFPNIMHD_00032 | 1.9e-51 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
GFPNIMHD_00033 | 7e-121 | G | PTS system mannose/fructose/sorbose family IID component | |||
GFPNIMHD_00034 | 3.8e-95 | G | PTS system sorbose-specific iic component | |||
GFPNIMHD_00035 | 1.8e-243 | cycA | E | Amino acid permease | ||
GFPNIMHD_00036 | 6.9e-215 | lmrP | E | Major Facilitator Superfamily | ||
GFPNIMHD_00037 | 7.8e-38 | |||||
GFPNIMHD_00038 | 5.2e-232 | 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 | ||
GFPNIMHD_00039 | 1.1e-169 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
GFPNIMHD_00040 | 2.3e-132 | L | An automated process has identified a potential problem with this gene model | |||
GFPNIMHD_00041 | 1.8e-12 | |||||
GFPNIMHD_00042 | 6.7e-116 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
GFPNIMHD_00043 | 1e-57 | 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 | ||
GFPNIMHD_00044 | 2.5e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
GFPNIMHD_00045 | 3.1e-95 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
GFPNIMHD_00046 | 6.4e-44 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
GFPNIMHD_00047 | 1.1e-227 | 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 | |
GFPNIMHD_00048 | 4.9e-57 | 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 | ||
GFPNIMHD_00049 | 2e-285 | pipD | E | Dipeptidase | ||
GFPNIMHD_00050 | 5e-166 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
GFPNIMHD_00051 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
GFPNIMHD_00052 | 7.8e-123 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
GFPNIMHD_00053 | 6.6e-133 | oppA | E | ABC transporter substrate-binding protein | ||
GFPNIMHD_00054 | 9e-264 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
GFPNIMHD_00055 | 1.7e-51 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
GFPNIMHD_00056 | 6.3e-224 | L | COG3547 Transposase and inactivated derivatives | |||
GFPNIMHD_00057 | 5.3e-167 | yjjC | V | ABC transporter | ||
GFPNIMHD_00058 | 7.4e-289 | M | Exporter of polyketide antibiotics | |||
GFPNIMHD_00059 | 3.6e-114 | K | Transcriptional regulator | |||
GFPNIMHD_00060 | 7.1e-289 | 1.3.5.4 | C | FMN_bind | ||
GFPNIMHD_00061 | 1.2e-20 | 1.3.5.4 | C | FMN_bind | ||
GFPNIMHD_00062 | 1.1e-50 | |||||
GFPNIMHD_00064 | 1.3e-104 | speG | J | Acetyltransferase (GNAT) domain | ||
GFPNIMHD_00065 | 3.3e-56 | |||||
GFPNIMHD_00066 | 1.9e-69 | K | Acetyltransferase (GNAT) domain | |||
GFPNIMHD_00067 | 4.1e-83 | FG | HIT domain | |||
GFPNIMHD_00068 | 3.4e-46 | S | MazG-like family | |||
GFPNIMHD_00069 | 7.7e-61 | |||||
GFPNIMHD_00070 | 1.6e-224 | 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 | |
GFPNIMHD_00071 | 2.1e-160 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
GFPNIMHD_00072 | 1.2e-62 | 2.5.1.74 | H | UbiA prenyltransferase family | ||
GFPNIMHD_00073 | 9.1e-146 | mrr | L | restriction endonuclease | ||
GFPNIMHD_00074 | 4.4e-59 | L | restriction endonuclease | |||
GFPNIMHD_00076 | 2.5e-15 | S | the current gene model (or a revised gene model) may contain one or more premature stops and or frameshifts | |||
GFPNIMHD_00077 | 6e-51 | M | Rib/alpha-like repeat | |||
GFPNIMHD_00078 | 4e-47 | arbZ | I | Acyltransferase | ||
GFPNIMHD_00079 | 6.8e-63 | arbZ | I | Acyltransferase | ||
GFPNIMHD_00080 | 4.1e-81 | S | Sterol carrier protein domain | |||
GFPNIMHD_00081 | 3.3e-46 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
GFPNIMHD_00082 | 2.7e-08 | |||||
GFPNIMHD_00083 | 9.4e-145 | G | Transmembrane secretion effector | |||
GFPNIMHD_00084 | 3.3e-47 | K | Helix-turn-helix domain | |||
GFPNIMHD_00085 | 4.4e-139 | F | DNA/RNA non-specific endonuclease | |||
GFPNIMHD_00086 | 5.1e-53 | L | nuclease | |||
GFPNIMHD_00087 | 2.8e-154 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
GFPNIMHD_00088 | 3.8e-185 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
GFPNIMHD_00089 | 1.8e-66 | metI | P | ABC transporter permease | ||
GFPNIMHD_00090 | 1e-265 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
GFPNIMHD_00091 | 1.7e-257 | frdC | 1.3.5.4 | C | FAD binding domain | |
GFPNIMHD_00092 | 1.4e-167 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
GFPNIMHD_00093 | 7.3e-245 | yjjP | S | Putative threonine/serine exporter | ||
GFPNIMHD_00094 | 5.5e-189 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
GFPNIMHD_00095 | 0.0 | aha1 | P | E1-E2 ATPase | ||
GFPNIMHD_00096 | 8.2e-307 | S | Bacterial membrane protein, YfhO | |||
GFPNIMHD_00097 | 3.4e-67 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
GFPNIMHD_00098 | 1.4e-170 | prmA | J | Ribosomal protein L11 methyltransferase | ||
GFPNIMHD_00099 | 3e-63 | |||||
GFPNIMHD_00100 | 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 | |
GFPNIMHD_00101 | 1.3e-73 | 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 | ||
GFPNIMHD_00102 | 3.1e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
GFPNIMHD_00103 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)