1tdw
From Proteopedia
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===Crystal structure of double truncated human phenylalanine hydroxylase BH4-responsive PKU mutant A313T.=== | ===Crystal structure of double truncated human phenylalanine hydroxylase BH4-responsive PKU mutant A313T.=== | ||
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{{ABSTRACT_PUBMED_15557004}} | {{ABSTRACT_PUBMED_15557004}} | ||
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| - | ==Disease== | ||
| - | Known disease associated with this structure: Phenylketonuria OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=612349 612349]], Hyperphenylalaninemia, mild OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=612349 612349]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1tdw]] is a 1 chain structure of [[Phenylalanine hydroxylase]] with 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=1TDW OCA]. | |
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| + | ==See Also== | ||
| + | *[[Phenylalanine hydroxylase|Phenylalanine hydroxylase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015557004</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Phenylalanine 4-monooxygenase]] | [[Category: Phenylalanine 4-monooxygenase]] | ||
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[[Category: Tyring, S.]] | [[Category: Tyring, S.]] | ||
[[Category: Ugarte, M.]] | [[Category: Ugarte, M.]] | ||
| + | [[Category: Oxidoreductase]] | ||
[[Category: Phenylalanine catabolism]] | [[Category: Phenylalanine catabolism]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 00:44:43 2009'' | ||
Revision as of 08:06, 27 July 2012
Contents |
Crystal structure of double truncated human phenylalanine hydroxylase BH4-responsive PKU mutant A313T.
Template:ABSTRACT PUBMED 15557004
About this Structure
1tdw is a 1 chain structure of Phenylalanine hydroxylase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Erlandsen H, Pey AL, Gamez A, Perez B, Desviat LR, Aguado C, Koch R, Surendran S, Tyring S, Matalon R, Scriver CR, Ugarte M, Martinez A, Stevens RC. Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations. Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16903-8. Epub 2004 Nov 19. PMID:15557004
