2nsx Summary

pdbe.org/2nsx
spacer

Structure of acid-beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease

The structure was published by Lieberman, R.L., Wustman, B.A., Huertas, P., et al., Schlossmacher, M.G., Ringe, D., and Petsko, G.A., in 2007 in a paper entitled "Structure of acid beta-glucosidase with pharmacological chaperone provides insight into Gaucher disease." (abstract).

This crystal structure was determined using X-ray diffraction at a resolution of 2.11 Å and deposited in 2006.

The experimental data on which the structure is based was also deposited.

This PDB entry contains multiple copies of the structure of Glucosylceramidase.

It also contains one or more heterogenic compounds (e.g., ligands, co-factors, ions, modified amino acids, etc.); see here for a complete list.

The molecule has more than one probable quaternary state observed. For more details see the quaternary structure page.

The following tables show cross-reference information to other databases (to obtain a list of all PDB entries sharing the same property or classification, click on the magnifying glass icon):


Chain Name UniProt Name of source organism % of UniProt sequence present in the sample Residues in the sample molecules % of residues observed
A Glucosylceramidase P04062 (40-536) (GLCM_HUMAN)search Homo sapienssearch 96% 497 100%
B Glucosylceramidase P04062 (40-536) (GLCM_HUMAN)search Homo sapienssearch 96% 497 100%
C Glucosylceramidase P04062 (40-536) (GLCM_HUMAN)search Homo sapienssearch 96% 497 100%
D Glucosylceramidase P04062 (40-536) (GLCM_HUMAN)search Homo sapienssearch 96% 497 100%


This entry contains 1 unique UniProt protein:

UniProt accession Name Organism PDB
P04062 (40 - 536) Glucosylceramidase Homo sapiens

Chain Structural classification (SCOP) Structural classification (CATH) Sequence family (Pfam)
A, B, C, D (P04062) Composite domain of glycosyl hydrolase families 5, 30, 39 and 51search, beta-glycanasessearch Glycosidasessearch, Golgi alpha-mannosidase IIsearch PF02055: O-Glycosyl hydrolase family 30search

Chain ID Cellular component (GO) Molecular function (GO) Biological process (GO)
A, B, C, D (P04062) lysosomesearch lysosomal membranesearch extracellular vesicular exosomesearch lysosomal lumensearch membranesearch protein bindingsearch hydrolase activitysearch glucosylceramidase activitysearch receptor bindingsearch hydrolase activity, acting on glycosyl bondssearch sphingolipid metabolic processsearch termination of signal transductionsearch response to thyroid hormonesearch response to pHsearch sphingosine biosynthetic processsearch response to testosteronesearch metabolic processsearch carbohydrate metabolic processsearch glucosylceramide catabolic processsearch negative regulation of interleukin-6 productionsearch ceramide biosynthetic processsearch response to estrogensearch lipid metabolic processsearch positive regulation of protein dephosphorylationsearch regulation of water loss via skinsearch skin morphogenesissearch response to glucocorticoidsearch small molecule metabolic processsearch cellular response to tumor necrosis factorsearch negative regulation of inflammatory responsesearch glycosphingolipid metabolic processsearch negative regulation of MAP kinase activitysearch

Chain InterPro annotation
A, B, C, D Glycoside hydrolase, family 30search Glycosyl hydrolase, family 13, all-betasearch Glycoside hydrolase, catalytic domainsearch Glycoside hydrolase superfamilysearch