1tg2
From Proteopedia
(Difference between revisions)
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==Disease== | ==Disease== | ||
| - | Known disease associated with this structure: Phenylketonuria OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id= | + | 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== | ||
| - | 1TG2 is a | + | 1TG2 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=1TG2 OCA]. |
==Reference== | ==Reference== | ||
| - | + | <ref group="xtra">PMID:15557004</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Phenylalanine 4-monooxygenase]] | [[Category: Phenylalanine 4-monooxygenase]] | ||
| - | [[Category: Single protein]] | ||
[[Category: Aguado, C.]] | [[Category: Aguado, C.]] | ||
[[Category: Desviat, L R.]] | [[Category: Desviat, L R.]] | ||
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[[Category: Phenylalanine hydroxylase phenylketonuria mutant a313t in complex with cofactor analogue 7,8-dihydrobiopterin]] | [[Category: Phenylalanine hydroxylase phenylketonuria mutant a313t in complex with cofactor analogue 7,8-dihydrobiopterin]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 11:39:01 2009'' |
Revision as of 09:39, 16 February 2009
Contents |
Crystal structure of phenylalanine hydroxylase A313T mutant with 7,8-dihydrobiopterin bound
Template:ABSTRACT PUBMED 15557004
Disease
Known disease associated with this structure: Phenylketonuria OMIM:[612349], Hyperphenylalaninemia, mild OMIM:[612349]
About this Structure
1TG2 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
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
Page seeded by OCA on Mon Feb 16 11:39:01 2009
Categories: Homo sapiens | Phenylalanine 4-monooxygenase | Aguado, C. | Desviat, L R. | Erlandsen, H. | Gamez, A. | Koch, R. | Martinez, A. | Matalon, R. | Perez, B. | Pey, A L. | Scriver, C R. | Stevens, R C. | Surendran, S. | Tyring, S. | Ugarte, M. | Phenylalanine hydroxylase phenylketonuria mutant a313t in complex with cofactor analogue 7,8-dihydrobiopterin
