2kbi
From Proteopedia
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==About this Structure== | ==About this Structure== | ||
- | 2KBI is a | + | 2KBI 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=2KBI OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:19074138</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: | + | [[Category: Balser, J R.]] |
- | [[Category: | + | [[Category: Chagot, B.]] |
+ | [[Category: Chazin, W J.]] | ||
+ | [[Category: Potet, F.]] | ||
[[Category: Brugada syndrome]] | [[Category: Brugada syndrome]] | ||
[[Category: Cardiomyopathy]] | [[Category: Cardiomyopathy]] | ||
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[[Category: Voltage-gated channel]] | [[Category: Voltage-gated channel]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 22 10:25:56 2009'' |
Revision as of 08:25, 22 March 2009
Contents |
Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5
Template:ABSTRACT PUBMED 19074138
Disease
Known disease associated with this structure: Brugada syndrome 1 OMIM:[600163], Cardiomyopathy, dilated, 1E OMIM:[600163], Heart block, nonprogressive OMIM:[600163], Heart block, progressive, type IA OMIM:[600163], Long QT syndrome-3 OMIM:[600163], Sick sinus syndrome 1 OMIM:[600163], Ventricular fibrillation, idiopathic OMIM:[600163], Sudden infant death syndrome, susceptibility to OMIM:[600163]
About this Structure
2KBI is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Chagot B, Potet F, Balser JR, Chazin WJ. Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5. J Biol Chem. 2009 Mar 6;284(10):6436-45. Epub 2008 Dec 11. PMID:19074138 doi:10.1074/jbc.M807747200
Page seeded by OCA on Sun Mar 22 10:25:56 2009
Categories: Homo sapiens | Balser, J R. | Chagot, B. | Chazin, W J. | Potet, F. | Brugada syndrome | Cardiomyopathy | Disease mutation | Ef-hand | Glycoprotein | Ion transport | Ionic channel | Long qt syndrome | Membrane | Metal binding protein | Phosphoprotein | Polymorphism | Protein | Sodium | Sodium channel | Sodium transport | Transmembrane | Transport | Ubl conjugation | Voltage-gated channel