Galactosylceramidase
From Proteopedia
(Difference between revisions)
Line 3: | Line 3: | ||
==Structure== | ==Structure== | ||
+ | X-ray diffraction data (<scene name='58/587874/Galactosylceramidase/1'>default scene</scene>) from mouse models indicates that GALC is an estimated 77 kDa protein consisting of 656 residues, which form a secondary structure containing 12 α-helices and 41 β-strands. Each β-strand contains three to eleven residues. | ||
== Function == | == Function == | ||
Line 8: | Line 9: | ||
== Disease == | == Disease == | ||
Defects in this enzyme cause the disease known in humans as Krabbe disease. Krabbe disease is a neurodegenerative disorder characterized by widespread demyelination caused by reduced or mutated function of GALC<ref name=Deane>PMID: 21876145</ref>. | Defects in this enzyme cause the disease known in humans as Krabbe disease. Krabbe disease is a neurodegenerative disorder characterized by widespread demyelination caused by reduced or mutated function of GALC<ref name=Deane>PMID: 21876145</ref>. | ||
+ | |||
== Relevance == | == Relevance == | ||
Revision as of 01:06, 3 June 2014
|
References
- ↑ doi: https://dx.doi.org/10.2210/pdb3zr5/pdb
- ↑ 2.0 2.1 Deane JE, Graham SC, Kim NN, Stein PE, McNair R, Cachon-Gonzalez MB, Cox TM, Read RJ. Insights into Krabbe disease from structures of galactocerebrosidase. Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15169-73. Epub 2011 Aug 29. PMID:21876145 doi:10.1073/pnas.1105639108
Proteopedia Page Contributors and Editors (what is this?)
Alison Stivers, Michal Harel, Dillon Shapiro, Angel Herraez, Joel L. Sussman