| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| FBNHIOJP_00001 | 2.7e-103 | |||||
| FBNHIOJP_00002 | 2.7e-129 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
| FBNHIOJP_00003 | 2.3e-98 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
| FBNHIOJP_00004 | 1.8e-187 | tsaD | 2.3.1.234 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
| FBNHIOJP_00005 | 3.6e-49 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | ||
| FBNHIOJP_00006 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
| FBNHIOJP_00007 | 4.2e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
| FBNHIOJP_00008 | 1e-60 | ytrA | K | helix_turn_helix gluconate operon transcriptional repressor | ||
| FBNHIOJP_00009 | 3e-159 | ytrB | V | ABC transporter | ||
| FBNHIOJP_00010 | 3.2e-187 | |||||
| FBNHIOJP_00011 | 1.1e-195 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
| FBNHIOJP_00012 | 4.2e-110 | ydiL | S | CAAX protease self-immunity | ||
| FBNHIOJP_00013 | 6.7e-44 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
| FBNHIOJP_00014 | 2.2e-293 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
| FBNHIOJP_00015 | 1.1e-56 | S | Domain of unknown function (DUF1827) | |||
| FBNHIOJP_00016 | 0.0 | ydaO | E | amino acid | ||
| FBNHIOJP_00017 | 4e-34 | L | Helix-turn-helix domain | |||
| FBNHIOJP_00018 | 2.2e-67 | L | hmm pf00665 | |||
| FBNHIOJP_00019 | 4.3e-64 | yugI | 5.3.1.9 | J | general stress protein | |
| FBNHIOJP_00020 | 1.7e-110 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
| FBNHIOJP_00021 | 4.7e-185 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
| FBNHIOJP_00022 | 1.5e-86 | pgpA | 3.1.3.27 | I | Phosphatidylglycerophosphatase A | |
| FBNHIOJP_00023 | 8.9e-116 | dedA | S | SNARE-like domain protein | ||
| FBNHIOJP_00024 | 7.3e-115 | S | Protein of unknown function (DUF1461) | |||
| FBNHIOJP_00025 | 1.7e-145 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
| FBNHIOJP_00026 | 2.6e-109 | yutD | S | Protein of unknown function (DUF1027) | ||
| FBNHIOJP_00027 | 1.3e-265 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
| FBNHIOJP_00028 | 5.3e-115 | S | Calcineurin-like phosphoesterase | |||
| FBNHIOJP_00029 | 5.9e-116 | yibF | S | overlaps another CDS with the same product name | ||
| FBNHIOJP_00030 | 1.9e-187 | yibE | S | overlaps another CDS with the same product name | ||
| FBNHIOJP_00031 | 6.1e-54 | |||||
| FBNHIOJP_00032 | 2.8e-257 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
| FBNHIOJP_00033 | 1.9e-272 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
| FBNHIOJP_00034 | 6.3e-134 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
| FBNHIOJP_00035 | 4e-127 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | HAD-hyrolase-like | |
| FBNHIOJP_00036 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | Penicillin binding protein transpeptidase domain |
| FBNHIOJP_00037 | 2.3e-179 | ccpA | K | catabolite control protein A | ||
| FBNHIOJP_00038 | 2.8e-215 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
| FBNHIOJP_00039 | 2.5e-92 | niaR | S | 3H domain | ||
| FBNHIOJP_00040 | 1.9e-78 | ytxH | S | YtxH-like protein | ||
| FBNHIOJP_00042 | 1.8e-156 | ykuT | M | mechanosensitive ion channel | ||
| FBNHIOJP_00043 | 2.7e-155 | XK27_00890 | S | Domain of unknown function (DUF368) | ||
| FBNHIOJP_00044 | 8.7e-84 | ykuL | S | CBS domain | ||
| FBNHIOJP_00045 | 5.2e-133 | gla | U | Major intrinsic protein | ||
| FBNHIOJP_00046 | 4.1e-95 | S | Phosphoesterase | |||
| FBNHIOJP_00047 | 5.3e-278 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
| FBNHIOJP_00048 | 1.2e-82 | yslB | S | Protein of unknown function (DUF2507) | ||
| FBNHIOJP_00049 | 5.5e-247 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
| FBNHIOJP_00050 | 1.2e-36 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
| FBNHIOJP_00051 | 4.5e-238 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
| FBNHIOJP_00052 | 1.2e-293 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
| FBNHIOJP_00053 | 6.6e-53 | trxA | O | Belongs to the thioredoxin family | ||
| FBNHIOJP_00054 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
| FBNHIOJP_00055 | 8.6e-93 | cvpA | S | Colicin V production protein | ||
| FBNHIOJP_00056 | 2e-36 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
| FBNHIOJP_00057 | 2.3e-53 | yrzB | S | Belongs to the UPF0473 family | ||
| FBNHIOJP_00058 | 2.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
| FBNHIOJP_00059 | 4e-43 | yrzL | S | Belongs to the UPF0297 family | ||
| FBNHIOJP_00060 | 3.9e-209 | |||||
| FBNHIOJP_00061 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
| FBNHIOJP_00062 | 4.3e-172 | |||||
| FBNHIOJP_00063 | 5.6e-250 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
| FBNHIOJP_00064 | 1.8e-178 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
| FBNHIOJP_00065 | 5.2e-240 | ytoI | K | DRTGG domain | ||
| FBNHIOJP_00066 | 3.1e-206 | 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 | |
| FBNHIOJP_00067 | 1.1e-289 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
| FBNHIOJP_00068 | 3.9e-116 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
| FBNHIOJP_00069 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
| FBNHIOJP_00070 | 1.4e-45 | yajC | U | Preprotein translocase | ||
| FBNHIOJP_00071 | 5.2e-228 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
| FBNHIOJP_00072 | 3.6e-207 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
| FBNHIOJP_00073 | 9e-195 | ruvB | 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 | |
| FBNHIOJP_00074 | 3.9e-102 | 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 | |
| FBNHIOJP_00075 | 3.5e-103 | yjbF | S | SNARE associated Golgi protein | ||
| FBNHIOJP_00076 | 1.6e-87 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
| FBNHIOJP_00077 | 2.7e-221 | yxjG | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | |
| FBNHIOJP_00078 | 7.6e-212 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
| FBNHIOJP_00079 | 1.4e-300 | frvR | K | Mga helix-turn-helix domain | ||
| FBNHIOJP_00080 | 2e-296 | frvR | K | Mga helix-turn-helix domain | ||
| FBNHIOJP_00081 | 9.4e-267 | lysP | E | amino acid | ||
| FBNHIOJP_00083 | 5.3e-130 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
| FBNHIOJP_00084 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
| FBNHIOJP_00085 | 1.6e-97 | |||||
| FBNHIOJP_00086 | 8.8e-98 | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | ||
| FBNHIOJP_00087 | 3.6e-188 | S | Bacterial protein of unknown function (DUF916) | |||
| FBNHIOJP_00088 | 9.9e-103 | |||||
| FBNHIOJP_00089 | 2e-18 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
| FBNHIOJP_00090 | 1.4e-156 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
| FBNHIOJP_00091 | 1.7e-156 | I | alpha/beta hydrolase fold | |||
| FBNHIOJP_00092 | 9.7e-48 | |||||
| FBNHIOJP_00093 | 2.5e-68 | |||||
| FBNHIOJP_00094 | 7.9e-46 | |||||
| FBNHIOJP_00095 | 1.5e-155 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
| FBNHIOJP_00096 | 7.2e-124 | citR | K | FCD | ||
| FBNHIOJP_00097 | 4.5e-266 | oadA | 2.1.3.1, 4.1.1.3, 6.4.1.1, 6.4.1.7 | C | Conserved carboxylase domain | |
| FBNHIOJP_00098 | 5.2e-101 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
| FBNHIOJP_00099 | 4.7e-285 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
| FBNHIOJP_00100 | 1.7e-154 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
| FBNHIOJP_00101 | 2.2e-48 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
| FBNHIOJP_00102 | 9.3e-181 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase |
Showing 1 to 100 of 2,560 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)