2kbi
From Proteopedia
| Line 23: | Line 23: | ||
==About this Structure== | ==About this Structure== | ||
| - | 2KBI is a | + | 2KBI 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=2KBI OCA]. |
==Reference== | ==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: | + | [[Category: Single protein]] |
| - | [[Category: | + | [[Category: Pdbx_ordinal=, <PDBx:audit_author.]] |
| - | + | ||
| - | + | ||
[[Category: Brugada syndrome]] | [[Category: Brugada syndrome]] | ||
[[Category: Cardiomyopathy]] | [[Category: Cardiomyopathy]] | ||
| Line 53: | Line 51: | ||
[[Category: Voltage-gated channel]] | [[Category: Voltage-gated channel]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 18 20: | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Mar 18 20:14:15 2009'' |
Revision as of 18:14, 18 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 Single protein 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[[Category: Pdbx_ordinal=, <PDBx:audit_author.]]
Page seeded by OCA on Wed Mar 18 20:14:15 2009
Categories: Homo sapiens | Single protein | 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
