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Glycoside Hydrolase Family 89

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Glycoside Hydrolase Family GH89
Clan none
Mechanism Retaining
Active site residues known
CAZy DB link
http://www.cazy.org/fam/GH89.html

Substrate specificities

The family 89 glycoside hydrolases are active as α-N-acetylglucosaminidases. The human lysosomal enzyme, NAGLU, is involved in the degradation of heparan sulfate. Mutations in this enzyme can cause a devastating disease called Sanfilippo syndrome type B which is also called mucopolysaccharidosis IIIB.

Kinetics and Mechanism

Mechanistic and structural data is available on CpGH89, a family 89 glycoside hydrolase produced by Clostridium perfringens. CpGH89 uses a double displacement mechanism to hydrolyze the glycosidic bond which results in retention of stereochemistry at the anomeric carbon.

Catalytic Residues

Two catalytically important glutamate residues have been identified in CpGH89, Glu483 and Glu601. These residues are between 6.1-6.7 Normal 0 false false false EN-CA X-NONE X-NONE MicrosoftInternetExplorer4 Å apart which is consistent with a retaining catalytic mechanism. Mutation of Glu601 to an Alanine results in an apparent abolishment of activity suggesting this residue is active as the catalytic nucleophile. Mutation of Glu483 to Alanine results in much less severe impairments in catalysis suggesting this residue is active as the catalytic acid/base residue. Glu483 is ~3.6Å from C1 and appears to be positioned in such a way that it is capable of forming a hydrogen bond with the glycosidic oxygen of the substrate.

Three-dimensional structures

Family Firsts

First sterochemistry determination
Cite some reference here, with a short explanation [1].
First catalytic nucleophile identification
First general acid/base residue identification
First 3-D structure

References

  1. Ficko-Blean E, Stubbs KA, Nemirovsky O, Vocadlo DJ, and Boraston AB. (2008). Structural and mechanistic insight into the basis of mucopolysaccharidosis IIIB. Proc Natl Acad Sci U S A. 2008;105(18):6560-5. DOI:10.1073/pnas.0711491105 | PubMed ID:18443291 [1]