2kbi: Difference between revisions
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==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: Pdbx_ordinal=, <PDBx:audit_author.]] | |||
[[Category: | |||
[[Category: Brugada syndrome]] | [[Category: Brugada syndrome]] | ||
[[Category: Cardiomyopathy]] | [[Category: Cardiomyopathy]] | ||
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[[Category: Voltage-gated channel]] | [[Category: Voltage-gated channel]] | ||
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Revision as of 21:14, 18 March 2009
Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5Solution NMR structure of the C-terminal EF-hand domain of human cardiac sodium channel NaV1.5
Template:ABSTRACT PUBMED 19074138
DiseaseDisease
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 StructureAbout this Structure
2KBI is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
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.]]
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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCA- Pages with broken file links
- 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