Galactosylceramidase
From Proteopedia
(Difference between revisions)
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<StructureSection load='3zr5' size='340' side='right' caption='Galactosylceramidase scene=''> | <StructureSection load='3zr5' size='340' side='right' caption='Galactosylceramidase scene=''> | ||
- | Galactosylceramidase (GALC) is a hydrolase <ref>DOI:10.2210/pdb3zr5/pdb</ref> ('''fix reference''') that removes galactose from ceramide derivatives ('''reference'''). Galactosylceramidase in humans is encoded by the gene GALC, and mutations in this gene are associated with Krabbe disease, or globoid cell leukodystrophy <ref>PMID: 21876145</ref>. | + | Galactosylceramidase (GALC) is a hydrolase <ref>DOI:10.2210/pdb3zr5/pdb</ref> ('''fix reference''') that removes galactose from ceramide derivatives ('''reference'''). Galactosylceramidase in humans is encoded by the gene GALC, and mutations in this gene are associated with Krabbe disease, or globoid cell leukodystrophy <ref name=Deane>PMID: 21876145</ref>. |
==Structure== | ==Structure== | ||
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== 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>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 22:51, 2 June 2014
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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
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