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InterPro: IPR011496 Beta-N-acetylglucosaminidase

Protein matchesHelp
UniProtKB
Matches:
196 proteins
AccessionHelp IPR011496 Beta-N-acetylglucosaminidase
TypeHelp Family
SignaturesHelp
InterPro annotation
BioMart Logo Entry Details in BioMart
AbstractHelp

This family consists of both eukaryotic and prokaryotic hyaluronidases. Human Q9HAR0 is expressed during meningioma [1]. Clostridium perfringens, P26831, is involved in pathogenesis and is likely to act on connectivity tissue during gas gangrene [2]. It catalyses the random hydrolysis of 1->4-linkages between N-acetyl-beta-D-glucosamine and D-glucuronate residues in hyaluronate.

Structural linksHelp
SCOP: c.1.8.10
Database linksHelp
Enzyme: EC:3.2.1.52
PANDIT: PF07555

Taxonomic coverageHelp

Example proteinsHelp
O60502 Bifunctional protein NCOAT

P26831 Hyaluronoglucosaminidase

Q8VIJ5 Bifunctional protein NCOAT

Q9EQQ9 Bifunctional protein NCOAT

More proteins


Example Proteins Key


InterPro entry accession number/name and structure databases Colour code
IPR016134 Cellulosome enzyme, dockerin type I
IPR018247 EF-Hand 1, calcium-binding site
IPR000421 Coagulation factor 5/8 type, C-terminal
IPR011490 Extracellular matrix-binding protein, Ebh
IPR008979 Galactose-binding domain-like
IPR016181 Acyl-CoA N-acyltransferase
IPR011496 Beta-N-acetylglucosaminidase
SWISS-MODEL
PDB Chain
ModBase

PublicationsHelp
1. Heckel D, Comtesse N, Brass N, Blin N, Zang KD, Meese E.
Novel immunogenic antigen homologous to hyaluronidase in meningioma.
Hum. Mol. Genet. 7 1859-72 1998 [PubMed: 9811929]
http://hmg.oxfordjournals.org/cgi/content/abstract/7/12/1859
2. Canard B, Garnier T, Saint-Joanis B, Cole ST.
Molecular genetic analysis of the nagH gene encoding a hyaluronidase of Clostridium perfringens.
Mol. Gen. Genet. 243 215-24 1994 [PubMed: 8177218]

Additional ReadingHelp
Whitworth GE, Macauley MS, Stubbs KA, Dennis RJ, Taylor EJ, Davies GJ, Greig IR, Vocadlo DJ.
Analysis of PUGNAc and NAG-thiazoline as transition state analogues for human O-GlcNAcase: mechanistic and structural insights into inhibitor selectivity and transition state poise.
J. Am. Chem. Soc. 129 2007 635-44 [PubMed: 17227027]
http://dx.doi.org/10.1021/ja065697o
Sheldon WL, Macauley MS, Taylor EJ, Robinson CE, Charnock SJ, Davies GJ, Vocadlo DJ, Black GW.
Functional analysis of a group A streptococcal glycoside hydrolase Spy1600 from family 84 reveals it is a beta-N-acetylglucosaminidase and not a hyaluronidase.
Biochem. J. 399 2006 241-7 [PubMed: 16822234]
http://dx.doi.org/10.1042/BJ20060307
Scaffidi A, Stubbs KA, Dennis RJ, Taylor EJ, Davies GJ, Vocadlo DJ, Stick RV.
A 1-acetamido derivative of 6-epi-valienamine: an inhibitor of a diverse group of beta-N-acetylglucosaminidases.
Org. Biomol. Chem. 5 2007 3013-9 [PubMed: 17728868]
http://dx.doi.org/10.1039/b709681j
Rao FV, Dorfmueller HC, Villa F, Allwood M, Eggleston IM, van Aalten DM.
Structural insights into the mechanism and inhibition of eukaryotic O-GlcNAc hydrolysis.
EMBO J. 25 2006 1569-78 [PubMed: 16541109]
http://dx.doi.org/10.1038/sj.emboj.7601026
Macauley MS, Bubb AK, Martinez-Fleites C, Davies GJ, Vocadlo DJ.
Elevation of global O-GlcNAc levels in 3T3-L1 adipocytes by selective inhibition of O-GlcNAcase does not induce insulin resistance.
J. Biol. Chem. 283 2008 34687-95 [PubMed: 18842583]
http://dx.doi.org/10.1074/jbc.M804525200
Yuzwa SA, Macauley MS, Heinonen JE, Shan X, Dennis RJ, He Y, Whitworth GE, Stubbs KA, McEachern EJ, Davies GJ, Vocadlo DJ.
A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo.
Nat. Chem. Biol. 4 2008 483-90 [PubMed: 18587388]
http://dx.doi.org/10.1038/nchembio.96
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InterPro 23.1