Galactosylceramidase

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==Structure==
==Structure==
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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 ==
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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 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>.
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== Relevance ==
== Relevance ==

Revision as of 01:06, 3 June 2014

PDB ID 3zr5

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References

  1. doi: https://dx.doi.org/10.2210/pdb3zr5/pdb
  2. 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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Alison Stivers, Michal Harel, Dillon Shapiro, Angel Herraez, Joel L. Sussman

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