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2rq8
From Proteopedia
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| - | + | [[Image:2rq8.png|left|200px]] | |
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{{ABSTRACT_PUBMED_20095049}} | {{ABSTRACT_PUBMED_20095049}} | ||
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| - | ==Disease== | ||
| - | Known disease associated with this structure: Cardiomyopathy, dilated, 1G OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188840 188840]], Cardiomyopathy, familial hypertrophic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188840 188840]], Muscular dystrophy, limb-girdle, type 2J OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188840 188840]], Myopathy, early-onset, with fatal cardiomyopathy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188840 188840]], Myopathy, proximal, with early respiratory muscle involvement OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188840 188840]], Tibial muscular dystrophy, tardive OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188840 188840]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[2rq8]] is a 1 chain structure of [[Titin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2RQ8 OCA]. | |
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| + | ==See Also== | ||
| + | *[[Titin]] | ||
==Reference== | ==Reference== | ||
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[[Category: Ubl conjugation]] | [[Category: Ubl conjugation]] | ||
[[Category: Wd repeat]] | [[Category: Wd repeat]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 3 09:45:41 2010'' | ||
Revision as of 20:46, 26 December 2010
Contents |
Solution NMR structure of titin I27 domain mutant
Template:ABSTRACT PUBMED 20095049
About this Structure
2rq8 is a 1 chain structure of Titin with sequence from Homo sapiens. Full experimental information is available from OCA.
See Also
Reference
- Yagawa K, Yamano K, Oguro T, Maeda M, Sato T, Momose T, Kawano S, Endo T. Structural basis for unfolding pathway-dependent stability of proteins: Vectorial unfolding vs. global unfolding. Protein Sci. 2010 Jan 21. PMID:20095049 doi:10.1002/pro.346
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Endo, T. | Kawano, S. | Momose, T. | Oguro, T. | Sato, T. | Yagawa, K. | Alternative splicing | Atp-binding | Beta-sandwich | Calcium | Calmodulin-binding | Cardiomyopathy | Coiled coil | Cytoplasm | Disease mutation | Disulfide bond | Immunoglobulin domain | Immunoglobulin-like domain | Isopeptide bond | Kelch repeat | Kinase | Limb-girdle muscular dystrophy | Magnesium | Metal-binding | Nucleotide-binding | Nucleus | Phosphoprotein | Polymorphism | Serine/threonine-protein kinase | Tpr repeat | Transferase | Ubl conjugation | Wd repeat
