1tg2 | pdb_00001tg2
From Proteopedia
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:[261600], Hyperphenylalaninemia, mild OMIM:[261600]
About this Structure
1TG2 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Correction of kinetic and stability defects by tetrahydrobiopterin in phenylketonuria patients with certain phenylalanine hydroxylase mutations., 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, 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 Sun Jul 27 13:42:16 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Phenylalanine 4-monooxygenase
- Single protein
- 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
