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CAZyme Information: MGYG000003659_00145

You are here: Home > Sequence: MGYG000003659_00145

Basic Information | Genomic context | Full Sequence | Enzyme annotations |  CAZy signature domains |  CDD domains | CAZyme hits | PDB hits | Swiss-Prot hits | SignalP and Lipop annotations | TMHMM annotations

Basic Information help

Species CAG-594 sp900771805
Lineage Bacteria; Firmicutes; Bacilli; RF39; UBA660; CAG-594; CAG-594 sp900771805
CAZyme ID MGYG000003659_00145
CAZy Family GT0
CAZyme Description UDP-N-acetylglucosamine 2-epimerase
CAZyme Property
Protein Length CGC Molecular Weight Isoelectric Point
369 42037.11 4.9705
Genome Property
Genome Assembly ID Genome Size Genome Type Country Continent
MGYG000003659 1207824 MAG Peru South America
Gene Location Start: 75759;  End: 76868  Strand: +

Full Sequence      Download help

MIKVMSIFGT  RPEAIKMAPL  VKELESRKEI  ESIVCVTAQH  REMLDQVLET  FDIKPDYDLN60
IMKQGQTLAE  VTTRALLGLE  EVIKEVKPDI  VLVHGDTTTT  FAGALAAFYN  QVAIGHVEAG120
LRTYDKYSPF  PEEMNRQMVD  CMTDMYFAPT  NLSKSNLLKQ  NIEESKIYVT  GNTAIDAMKT180
TVDKDYSNEV  LDWVGNDRMI  LLTAHRRENL  GDPMRHIFKA  IKRIVDEFDD  IKVVYPIHMN240
PRVREVAKEI  FSNCDRIRLI  EPLEVFDFHN  FQNKSYIILS  DSGGIQEEAP  SLGKPVLVLR300
DTTERPEGIE  AGTLKLVGTN  EETIYKETKK  LLTDKAEYDR  MSKASNPYGD  GHTSERIADA360
IIEKFNKEY369

Enzyme Prediction      help

No EC number prediction in MGYG000003659_00145.

CDD Domains      download full data without filtering help

Created with Snap18365573921101291471661842022212392582762953133323501366WecB2361wecB3362GTB_UDP-GlcNAc_2-Epimerase22361Epimerase_279363GT28_Beta-DGS-like
Cdd ID Domain E-Value qStart qEnd sStart sEnd Domain Description
COG0381 WecB 0.0 1 366 3 373
UDP-N-acetylglucosamine 2-epimerase [Cell wall/membrane/envelope biogenesis].
TIGR00236 wecB 0.0 2 361 1 361
UDP-N-acetylglucosamine 2-epimerase. This cytosolic enzyme converts UDP-N-acetyl-D-glucosamine to UDP-N-acetyl-D-mannosamine. In E. coli, this is the first step in the pathway of enterobacterial common antigen biosynthesis.Members of this orthology group have many gene symbols, often reflecting the overall activity of the pathway and/or operon that includes it. Symbols include epsC (exopolysaccharide C) in Burkholderia solanacerum, cap8P (type 8 capsule P) in Staphylococcus aureus, and nfrC in an older designation based on the effects of deletion on phage N4 adsorption. Epimerase activity was also demonstrated in a bifunctional rat enzyme, for which the N-terminal domain appears to be orthologous. The set of proteins found above the suggested cutoff includes E. coli WecB in one of two deeply branched clusters and the rat UDP-N-acetylglucosamine 2-epimerase domain in the other. [Cell envelope, Biosynthesis and degradation of surface polysaccharides and lipopolysaccharides]
cd03786 GTB_UDP-GlcNAc_2-Epimerase 1.87e-168 3 362 1 365
UDP-N-acetylglucosamine 2-epimerase and similar proteins. Bacterial members of the UDP-N-Acetylglucosamine (GlcNAc) 2-Epimerase family (EC 5.1.3.14) are known to catalyze the reversible interconversion of UDP-GlcNAc and UDP-N-acetylmannosamine (UDP-ManNAc). The enzyme serves to produce an activated form of ManNAc residues (UDP-ManNAc) for use in the biosynthesis of a variety of cell surface polysaccharides; The mammalian enzyme is bifunctional, catalyzing both the inversion of stereochemistry at C-2 and the hydrolysis of the UDP-sugar linkage to generate free ManNAc. It also catalyzes the phosphorylation of ManNAc to generate ManNAc 6-phosphate, a precursor to salic acids. In mammals, sialic acids are found at the termini of oligosaccharides in a large variety of cell surface glycoconjugates and are key mediators of cell-cell recognition events. Mutations in human members of this family have been associated with Sialuria, a rare disease caused by the disorders of sialic acid metabolism. This family belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.
pfam02350 Epimerase_2 1.55e-159 22 361 1 335
UDP-N-acetylglucosamine 2-epimerase. This family consists of UDP-N-acetylglucosamine 2-epimerases EC:5.1.3.14 this enzyme catalyzes the production of UDP-ManNAc from UDP-GlcNAc. Note that some of the enzymes is this family are bifunctional, in these instances Pfam matches only the N-terminal half of the protein suggesting that the additional C-terminal part (when compared to mono-functional members of this family) is responsible for the UPD-N-acetylmannosamine kinase activity of these enzymes. This hypothesis is further supported by the assumption that the C-terminal part of rat Gne is the kinase domain.
cd17507 GT28_Beta-DGS-like 3.41e-05 79 363 89 361
beta-diglucosyldiacylglycerol synthase and similar proteins. beta-diglucosyldiacylglycerol synthase (processive diacylglycerol beta-glucosyltransferase EC 2.4.1.315) is involved in the biosynthesis of both the bilayer- and non-bilayer-forming membrane glucolipids. This family of glycosyltransferases also contains plant major galactolipid synthase (chloroplastic monogalactosyldiacylglycerol synthase 1 EC 2.4.1.46). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.

CAZyme Hits      help

Created with Snap18365573921101291471661842022212392582762953133323503361QLA08260.1|GT03361AUV68874.1|GT03361AUV66492.1|GT03361AMW24368.1|GT03361AVH46190.1|GT0
Hit ID E-Value Query Start Query End Hit Start Hit End
QLA08260.1 6.58e-177 3 361 3 361
AUV68874.1 1.26e-175 3 361 3 361
AUV66492.1 1.26e-175 3 361 3 361
AMW24368.1 7.24e-175 3 361 3 361
AVH46190.1 2.94e-174 3 361 3 361

PDB Hits      download full data without filtering help

Created with Snap183655739211012914716618420222123925827629531333235023624FKZ_A23673BEO_A23621O6C_A33615ENZ_A23673OT5_A
Hit ID E-Value Query Start Query End Hit Start Hit End Description
4FKZ_A 7.44e-183 2 362 4 364
Crystalstructure of Bacillus subtilis UDP-GlcNAc 2-epimerase in complex with UDP-GlcNAc and UDP [Bacillus subtilis subsp. subtilis str. 168],4FKZ_B Crystal structure of Bacillus subtilis UDP-GlcNAc 2-epimerase in complex with UDP-GlcNAc and UDP [Bacillus subtilis subsp. subtilis str. 168]
3BEO_A 2.69e-182 2 367 9 375
AStructural Basis for the allosteric regulation of non-hydrolyzing UDP-GlcNAc 2-epimerases [Bacillus anthracis],3BEO_B A Structural Basis for the allosteric regulation of non-hydrolyzing UDP-GlcNAc 2-epimerases [Bacillus anthracis]
1O6C_A 2.98e-175 2 362 4 364
Crystalstructure of UDP-N-acetylglucosamine 2-epimerase [Bacillus subtilis],1O6C_B Crystal structure of UDP-N-acetylglucosamine 2-epimerase [Bacillus subtilis]
5ENZ_A 2.77e-170 3 361 3 361
S.aureus MnaA-UDP co-structure [Staphylococcus aureus],5ENZ_B S. aureus MnaA-UDP co-structure [Staphylococcus aureus]
3OT5_A 1.08e-164 2 367 28 394
2.2Angstrom Resolution Crystal Structure of putative UDP-N-acetylglucosamine 2-epimerase from Listeria monocytogenes [Listeria monocytogenes EGD-e],3OT5_B 2.2 Angstrom Resolution Crystal Structure of putative UDP-N-acetylglucosamine 2-epimerase from Listeria monocytogenes [Listeria monocytogenes EGD-e],3OT5_C 2.2 Angstrom Resolution Crystal Structure of putative UDP-N-acetylglucosamine 2-epimerase from Listeria monocytogenes [Listeria monocytogenes EGD-e],3OT5_D 2.2 Angstrom Resolution Crystal Structure of putative UDP-N-acetylglucosamine 2-epimerase from Listeria monocytogenes [Listeria monocytogenes EGD-e]

Swiss-Prot Hits      download full data without filtering help

Created with Snap18365573921101291471661842022212392582762953133323502362sp|P39131|MNAA_BACSU1365sp|Q9X0C4|Y1034_THEMA2365sp|P45360|Y2874_CLOAB3361sp|Q8XAR8|WECB_ECO573361sp|P27828|WECB_ECOLI
Hit ID E-Value Query Start Query End Hit Start Hit End Description
P39131 3.06e-182 2 362 4 364
UDP-N-acetylglucosamine 2-epimerase OS=Bacillus subtilis (strain 168) OX=224308 GN=mnaA PE=1 SV=1
Q9X0C4 5.93e-158 1 365 1 368
Putative UDP-N-acetylglucosamine 2-epimerase OS=Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) OX=243274 GN=TM_1034 PE=3 SV=1
P45360 1.70e-149 2 365 4 371
Putative UDP-N-acetylglucosamine 2-epimerase OS=Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) OX=272562 GN=CA_C2874 PE=3 SV=2
Q8XAR8 5.63e-131 3 361 2 369
UDP-N-acetylglucosamine 2-epimerase OS=Escherichia coli O157:H7 OX=83334 GN=wecB PE=3 SV=1
P27828 1.13e-130 3 361 2 369
UDP-N-acetylglucosamine 2-epimerase OS=Escherichia coli (strain K12) OX=83333 GN=wecB PE=1 SV=2

SignalP and Lipop Annotations help

This protein is predicted as OTHER

Other SP_Sec_SPI LIPO_Sec_SPII TAT_Tat_SPI TATLIP_Sec_SPII PILIN_Sec_SPIII
1.000035 0.000000 0.000000 0.000000 0.000000 0.000000

TMHMM  Annotations      help

There is no transmembrane helices in MGYG000003659_00145.