3exf
From Proteopedia
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===Crystal structure of the pyruvate dehydrogenase (E1p) component of human pyruvate dehydrogenase complex=== | ===Crystal structure of the pyruvate dehydrogenase (E1p) component of human pyruvate dehydrogenase complex=== | ||
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==About this Structure== | ==About this Structure== | ||
3EXF is a 8 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3EXF OCA]. | 3EXF is a 8 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3EXF OCA]. | ||
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| + | ==Reference== | ||
| + | Structural basis for inactivation of the human pyruvate dehydrogenase complex by phosphorylation: role of disordered phosphorylation loops., Kato M, Wynn RM, Chuang JL, Tso SC, Machius M, Li J, Chuang DT, Structure. 2008 Dec 12;16(12):1849-59. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/19081061 19081061] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Chuang, D T.]] | [[Category: Chuang, D T.]] | ||
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[[Category: Transit peptide]] | [[Category: Transit peptide]] | ||
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Revision as of 10:51, 14 January 2009
Crystal structure of the pyruvate dehydrogenase (E1p) component of human pyruvate dehydrogenase complex
Template:ABSTRACT PUBMED 19081061
About this Structure
3EXF is a 8 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Structural basis for inactivation of the human pyruvate dehydrogenase complex by phosphorylation: role of disordered phosphorylation loops., Kato M, Wynn RM, Chuang JL, Tso SC, Machius M, Li J, Chuang DT, Structure. 2008 Dec 12;16(12):1849-59. PMID:19081061
Page seeded by OCA on Wed Jan 14 12:51:08 2009
Categories: Homo sapiens | Chuang, D T. | Chuang, J L. | Kato, M. | Li, J. | Machius, M. | Tso, S C. | Wynn, R M. | Alternative splicing | Disease mutation | Glycolysis | Heterotetramer | Leigh syndrome | Mitochondrion | Oxidoreductase | Phosphoprotein | Polymorphism | Pyruvate | Thiamine diphosphate-dependent enzyme | Thiamine pyrophosphate | Transit peptide
