2cqy: Difference between revisions
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{{STRUCTURE_2cqy| PDB=2cqy | SCENE= }} | {{STRUCTURE_2cqy| PDB=2cqy | SCENE= }} | ||
===Solution structure of B domain from human propionyl-CoA carboxylase alpha subunit=== | ===Solution structure of B domain from human propionyl-CoA carboxylase alpha subunit=== | ||
==Disease== | |||
[[http://www.uniprot.org/uniprot/PCCA_HUMAN PCCA_HUMAN]] Defects in PCCA are the cause of propionic acidemia type I (PA-1) [MIM:[http://omim.org/entry/606054 606054]]. PA-1 is a life-threatening disease characterized by episodic vomiting, lethargy and ketosis, neutropenia, periodic thrombocytopenia, hypogammaglobulinemia, developmental retardation, and intolerance to protein.<ref>PMID:10101253</ref><ref>PMID:12559849</ref><ref>PMID:15059621</ref><ref>PMID:10329019</ref> | |||
==About this Structure== | ==About this Structure== | ||
[[2cqy]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CQY OCA]. | [[2cqy]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CQY OCA]. | ||
==Reference== | |||
<references group="xtra"/><references/> | |||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Propionyl-CoA carboxylase]] | [[Category: Propionyl-CoA carboxylase]] | ||
