3hy8
From Proteopedia
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| + | [[Image:3hy8.png|left|200px]] | ||
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| + | {{STRUCTURE_3hy8| PDB=3hy8 | SCENE= }} | ||
| - | + | ===Crystal Structure of Human Pyridoxine 5'-Phosphate Oxidase R229W Mutant=== | |
| - | Description: Crystal Structure of Human Pyridoxine 5'-Phosphate Oxidase R229W Mutant | ||
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| + | {{ABSTRACT_PUBMED_19759001}} | ||
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| + | ==Disease== | ||
| + | Known disease associated with this structure: Pyridoxamine 5 -phosphate oxidase deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603287 603287]] | ||
| + | |||
| + | ==About this Structure== | ||
| + | 3HY8 is a 1 chain structure of sequence 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=3HY8 OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19759001</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Pyridoxal 5'-phosphate synthase]] | ||
| + | [[Category: Musayev, F N.]] | ||
| + | [[Category: Saavedra, M K.]] | ||
| + | [[Category: Safo, M K.]] | ||
| + | [[Category: Salvo, M L.Di.]] | ||
| + | [[Category: Schirch, V.]] | ||
| + | [[Category: Disease mutation]] | ||
| + | [[Category: Epilepsy]] | ||
| + | [[Category: Flavoprotein]] | ||
| + | [[Category: Fmn]] | ||
| + | [[Category: Fmn binding protein]] | ||
| + | [[Category: Oxidase]] | ||
| + | [[Category: Oxidoreductase]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Pyridoxal phosphate]] | ||
| + | [[Category: Pyridoxine biosynthesis]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 16 11:08:14 2009'' | ||
Revision as of 09:08, 16 December 2009
Contents |
Crystal Structure of Human Pyridoxine 5'-Phosphate Oxidase R229W Mutant
Template:ABSTRACT PUBMED 19759001
Disease
Known disease associated with this structure: Pyridoxamine 5 -phosphate oxidase deficiency OMIM:[603287]
About this Structure
3HY8 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Musayev FN, Di Salvo ML, Saavedra MA, Contestabile R, Ghatge MS, Haynes A, Schirch V, Safo MK. Molecular basis of reduced pyridoxine 5'-phosphate oxidase catalytic activity in neonatal epileptic encephalopathy disorder. J Biol Chem. 2009 Nov 6;284(45):30949-56. Epub 2009 Sep 15. PMID:19759001 doi:10.1074/jbc.M109.038372
Page seeded by OCA on Wed Dec 16 11:08:14 2009
Categories: Homo sapiens | Pyridoxal 5'-phosphate synthase | Musayev, F N. | Saavedra, M K. | Safo, M K. | Salvo, M L.Di. | Schirch, V. | Disease mutation | Epilepsy | Flavoprotein | Fmn | Fmn binding protein | Oxidase | Oxidoreductase | Phosphoprotein | Polymorphism | Pyridoxal phosphate | Pyridoxine biosynthesis
