2kbi
From Proteopedia
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===Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5=== | ===Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5=== | ||
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==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
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]. | 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]. | ||
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| + | ==Reference== | ||
| + | Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5., Chagot B, Potet F, Balser JR, Chazin WJ, J Biol Chem. 2008 Dec 11. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/19074138 19074138] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Balser, J R.]] | [[Category: Balser, J R.]] | ||
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[[Category: Voltage-gated channel]] | [[Category: Voltage-gated channel]] | ||
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Revision as of 07:05, 31 December 2008
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]
About this Structure
2KBI is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5., Chagot B, Potet F, Balser JR, Chazin WJ, J Biol Chem. 2008 Dec 11. PMID:19074138
Page seeded by OCA on Wed Dec 31 09:05:57 2008
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
