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Disulfide Connectivity of Velaglucerase
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<applet load='1ogs' size='[450,338]' frame='true' align='right' | <applet load='1ogs' size='[450,338]' frame='true' align='right' | ||
| - | caption='Human beta-glucocerebrosidase (1ogs)' scene='User:Adriana_Kita/Sandbox_1/Gcase_whole/5'/> | + | caption='Human beta-glucocerebrosidase (1ogs)<ref>FDvir H, Harel M, McCarthy AA, Toker L, Silman I, Futerman AH, Sussman JL, EMBO Rep. 2003 Jul;4(7):704-9. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/14764885 12792654]</ref>' scene='User:Adriana_Kita/Sandbox_1/Gcase_whole/5'/> |
Human beta-glucocerebrosidase, also known as glucoceremidase, GCase, and velaglucerase, is an enzyme that is commonly found to be deficient in patients with Gaucher's disease. | Human beta-glucocerebrosidase, also known as glucoceremidase, GCase, and velaglucerase, is an enzyme that is commonly found to be deficient in patients with Gaucher's disease. | ||
Revision as of 08:56, 1 May 2010
Human beta-glucocerebrosidase
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Proteopedia Page Contributors and Editors (what is this?)
Joel L. Sussman, Michal Harel, Wayne Decatur, Adriana Kita, David Canner
Categories: Glucosylceramidase | Single protein | Dvir, H. | Futerman, A H. | Harel, M. | ISPC, Israel Structural Proteomics Center. | Mccarthy, A A. | Silman, I. | Sussman, J L. | Toker, L. | Alternative initiation | Cerezyme hydrolase | Disease mutati polymorphism | Gaucher disease | Glucocerebrosidase | Glucosidase | Glycoprote lysosome | Glycosidase | ISPC | Israel Structural Proteomics Center | Membrane | Pharmaceutical | Signal | Sphingolipid metabolism | Structural genomic
