1wsv: Difference between revisions
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{{STRUCTURE_1wsv| PDB=1wsv | SCENE= }} | {{STRUCTURE_1wsv| PDB=1wsv | SCENE= }} | ||
===Crystal Structure of Human T-protein of Glycine Cleavage System=== | |||
{{ABSTRACT_PUBMED_16051266}} | |||
=== | ==Disease== | ||
[[http://www.uniprot.org/uniprot/GCST_HUMAN GCST_HUMAN]] Defects in AMT are a cause of non-ketotic hyperglycinemia (NKH) [MIM:[http://omim.org/entry/605899 605899]]; also known as glycine encephalopathy (GCE). NKH is an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms.<ref>PMID:8005589</ref><ref>PMID:9600239</ref><ref>PMID:9621520</ref><ref>PMID:10873393</ref><ref>PMID:11286506</ref> | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/GCST_HUMAN GCST_HUMAN]] The glycine cleavage system catalyzes the degradation of glycine. | |||
==About this Structure== | ==About this Structure== | ||
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==Reference== | ==Reference== | ||
<ref group="xtra">PMID:016051266</ref><references group="xtra"/> | <ref group="xtra">PMID:016051266</ref><references group="xtra"/><references/> | ||
[[Category: Aminomethyltransferase]] | [[Category: Aminomethyltransferase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
