1tg2: Difference between revisions

Line 20:

==Disease==

Known disease associated with this structure: Phenylketonuria OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=~~261600 261600~~]], Hyperphenylalaninemia, mild OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=~~261600 261600~~]]

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==

1TG2 is a ~~[[Single protein]]~~ 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].

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==

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:~~[http:~~//~~www.ncbi.nlm.nih.gov/pubmed/15557004 15557004]~~

[[Category: Homo sapiens]]

[[Category: Phenylalanine 4-monooxygenase]]

~~[[Category: Single protein]]~~

[[Category: Aguado, C.]]

[[Category: Desviat, L R.]]

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[[Category: Phenylalanine hydroxylase phenylketonuria mutant a313t in complex with cofactor analogue 7,8-dihydrobiopterin]]

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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 11:39:01 2009''

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@@ Line 20: / Line 20: @@
 ==Disease==
-Known disease associated with this structure: Phenylketonuria OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261600 261600]], Hyperphenylalaninemia, mild OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261600 261600]]
+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==
-TG2 is a [[Single protein]] 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].
+TG2 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==
-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:[http://www.ncbi.nlm.nih.gov/pubmed/15557004 15557004]
+<ref group="xtra">PMID:15557004</ref><references group="xtra"/>
 [[Category: Homo sapiens]]
 [[Category: Phenylalanine 4-monooxygenase]]
-[[Category: Single protein]]
 [[Category: Aguado, C.]]
 [[Category: Desviat, L R.]]
@@ Line 46: / Line 45: @@
 [[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 Sun Jul 27 13:42:16 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 11:39:01 2009''