1pwa
From Proteopedia
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{{STRUCTURE_1pwa| PDB=1pwa | SCENE= }} | {{STRUCTURE_1pwa| PDB=1pwa | SCENE= }} | ||
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===Crystal structure of Fibroblast Growth Factor 19=== | ===Crystal structure of Fibroblast Growth Factor 19=== | ||
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{{ABSTRACT_PUBMED_14730967}} | {{ABSTRACT_PUBMED_14730967}} | ||
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+ | ==Function== | ||
+ | [[http://www.uniprot.org/uniprot/FGF19_HUMAN FGF19_HUMAN]] Involved in the suppression of bile acid biosynthesis through down-regulation of CYP7A1 expression, following positive regulation of the JNK and ERK1/2 cascades. Stimulates glucose uptake in adipocytes. Activity requires the presence of KLB and FGFR4.<ref>PMID:12815072</ref> <ref>PMID:16597617</ref> <ref>PMID:17623664</ref> <ref>PMID:19085950</ref> | ||
==About this Structure== | ==About this Structure== | ||
- | [[1pwa]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/ | + | [[1pwa]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PWA OCA]. |
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+ | ==See Also== | ||
+ | *[[Fibroblast growth factor|Fibroblast growth factor]] | ||
==Reference== | ==Reference== | ||
- | <ref group="xtra">PMID:014730967</ref><references group="xtra"/> | + | <ref group="xtra">PMID:014730967</ref><references group="xtra"/><references/> |
- | [[Category: | + | [[Category: Human]] |
[[Category: Blundell, T L.]] | [[Category: Blundell, T L.]] | ||
[[Category: Chirgadze, D.]] | [[Category: Chirgadze, D.]] |
Revision as of 08:17, 16 April 2014
Contents |
Crystal structure of Fibroblast Growth Factor 19
Template:ABSTRACT PUBMED 14730967
Function
[FGF19_HUMAN] Involved in the suppression of bile acid biosynthesis through down-regulation of CYP7A1 expression, following positive regulation of the JNK and ERK1/2 cascades. Stimulates glucose uptake in adipocytes. Activity requires the presence of KLB and FGFR4.[1] [2] [3] [4]
About this Structure
1pwa is a 1 chain structure with sequence from Human. Full crystallographic information is available from OCA.
See Also
Reference
- Harmer NJ, Pellegrini L, Chirgadze D, Fernandez-Recio J, Blundell TL. The crystal structure of fibroblast growth factor (FGF) 19 reveals novel features of the FGF family and offers a structural basis for its unusual receptor affinity. Biochemistry. 2004 Jan 27;43(3):629-40. PMID:14730967 doi:10.1021/bi035320k
- ↑ Holt JA, Luo G, Billin AN, Bisi J, McNeill YY, Kozarsky KF, Donahee M, Wang DY, Mansfield TA, Kliewer SA, Goodwin B, Jones SA. Definition of a novel growth factor-dependent signal cascade for the suppression of bile acid biosynthesis. Genes Dev. 2003 Jul 1;17(13):1581-91. Epub 2003 Jun 18. PMID:12815072 doi:10.1101/gad.1083503
- ↑ Zhang X, Ibrahimi OA, Olsen SK, Umemori H, Mohammadi M, Ornitz DM. Receptor specificity of the fibroblast growth factor family. The complete mammalian FGF family. J Biol Chem. 2006 Jun 9;281(23):15694-700. Epub 2006 Apr 4. PMID:16597617 doi:10.1074/jbc.M601252200
- ↑ Kurosu H, Choi M, Ogawa Y, Dickson AS, Goetz R, Eliseenkova AV, Mohammadi M, Rosenblatt KP, Kliewer SA, Kuro-o M. Tissue-specific expression of betaKlotho and fibroblast growth factor (FGF) receptor isoforms determines metabolic activity of FGF19 and FGF21. J Biol Chem. 2007 Sep 14;282(37):26687-95. Epub 2007 Jul 10. PMID:17623664 doi:10.1074/jbc.M704165200
- ↑ Song KH, Li T, Owsley E, Strom S, Chiang JY. Bile acids activate fibroblast growth factor 19 signaling in human hepatocytes to inhibit cholesterol 7alpha-hydroxylase gene expression. Hepatology. 2009 Jan;49(1):297-305. doi: 10.1002/hep.22627. PMID:19085950 doi:http://dx.doi.org/10.1002/hep.22627