3bic
From Proteopedia
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[[Image:3bic.jpg|left|200px]] | [[Image:3bic.jpg|left|200px]] | ||
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| - | | | + | {{STRUCTURE_3bic| PDB=3bic | SCENE= }} |
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'''Crystal structure of human methylmalonyl-CoA mutase''' | '''Crystal structure of human methylmalonyl-CoA mutase''' | ||
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[[Category: Ugochukwu, E.]] | [[Category: Ugochukwu, E.]] | ||
[[Category: Weigelt, J.]] | [[Category: Weigelt, J.]] | ||
| - | [[Category: | + | [[Category: Cobalamin]] |
| - | [[Category: | + | [[Category: Cobalt]] |
| - | [[Category: | + | [[Category: Disease mutation]] |
| - | [[Category: | + | [[Category: Isomerase]] |
| - | [[Category: | + | [[Category: Metabolic disease]] |
| - | [[Category: | + | [[Category: Metal-binding]] |
| - | [[Category: | + | [[Category: Methylmalonyl coa mutase deficiency]] |
| - | [[Category: | + | [[Category: Mitochondrion]] |
| - | [[Category: | + | [[Category: Organic aciduria]] |
| - | [[Category: | + | [[Category: Polymorphism]] |
| - | [[Category: | + | [[Category: Sgc]] |
| - | [[Category: | + | [[Category: Structural genomic]] |
| - | [[Category: | + | [[Category: Structural genomics consortium]] |
| - | [[Category: | + | [[Category: Transit peptide]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 20:48:11 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 17:48, 4 May 2008
Crystal structure of human methylmalonyl-CoA mutase
Disease
Known disease associated with this structure: Methylmalonic aciduria, mut(0) type OMIM:[609058]
About this Structure
3BIC is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA. Page seeded by OCA on Sun May 4 20:48:11 2008
Categories: Homo sapiens | Methylmalonyl-CoA mutase | Single protein | Arrowsmith, C H. | Delft, F von. | Edwards, A M. | Gileadi, O. | Kochan, G. | Oppermann, U. | Pantic, N. | Parizotto, E. | Pike, A C.W. | Pilka, E S. | SGC, Structural Genomics Consortium. | Ugochukwu, E. | Weigelt, J. | Cobalamin | Cobalt | Disease mutation | Isomerase | Metabolic disease | Metal-binding | Methylmalonyl coa mutase deficiency | Mitochondrion | Organic aciduria | Polymorphism | Sgc | Structural genomic | Structural genomics consortium | Transit peptide
