4xwh | pdb_00004xwh
From Proteopedia
Crystal structure of the human N-acetyl-alpha-glucosaminidase
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Structural highlights
Disease[ANAG_HUMAN] Sanfilippo syndrome type B. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Function[ANAG_HUMAN] Involved in the degradation of heparan sulfate. Contents | ||||||||||||||||||||||
This page was last modified 15:50, 3 February 2016.