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{{STRUCTURE_3knb| PDB=3knb | SCENE= }} | |||
===Crystal structure of the titin C-terminus in complex with obscurin-like 1=== | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | ==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== | |||
3KNB is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=3irg 3irg]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3KNB OCA]. | |||
[[Category: Homo sapiens]] | |||
[[Category: Non-specific serine/threonine protein kinase]] | |||
[[Category: F., Sauer.]] | |||
[[Category: J., Vahokoski.]] | |||
[[Category: M., Wilmanns.]] | |||
[[Category: Alternative splicing]] | |||
[[Category: Atp-binding]] | |||
[[Category: Calcium]] | |||
[[Category: Calmodulin-binding]] | |||
[[Category: Cardiomyopathy]] | |||
[[Category: Cytoplasm]] | |||
[[Category: Disease mutation]] | |||
[[Category: Ig-like]] | |||
[[Category: Immunoglobulin domain]] | |||
[[Category: Kinase]] | |||
[[Category: Limb-girdle muscular dystrophy]] | |||
[[Category: Magnesium]] | |||
[[Category: Nucleotide-binding]] | |||
[[Category: Nucleus]] | |||
[[Category: Obscurin]] | |||
[[Category: Obsl1]] | |||
[[Category: Phosphoprotein]] | |||
[[Category: Polymorphism]] | |||
[[Category: Serine/threonine-protein kinase]] | |||
[[Category: Titin]] | |||
[[Category: Transferase]] | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 2 09:48:26 2009'' |
Revision as of 10:48, 2 December 2009
Crystal structure of the titin C-terminus in complex with obscurin-like 1Crystal structure of the titin C-terminus in complex with obscurin-like 1
DiseaseDisease
Known disease associated with this structure: Cardiomyopathy, dilated, 1G OMIM:[188840], Cardiomyopathy, familial hypertrophic OMIM:[188840], Muscular dystrophy, limb-girdle, type 2J OMIM:[188840], Myopathy, early-onset, with fatal cardiomyopathy OMIM:[188840], Myopathy, proximal, with early respiratory muscle involvement OMIM:[188840], Tibial muscular dystrophy, tardive OMIM:[188840]
About this StructureAbout this Structure
3KNB is a 2 chains structure of sequences from Homo sapiens. This structure supersedes the now removed PDB entry 3irg. Full crystallographic information is available from OCA.
Page seeded by OCA on Wed Dec 2 09:48:26 2009
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- Homo sapiens
- Non-specific serine/threonine protein kinase
- F., Sauer.
- J., Vahokoski.
- M., Wilmanns.
- Alternative splicing
- Atp-binding
- Calcium
- Calmodulin-binding
- Cardiomyopathy
- Cytoplasm
- Disease mutation
- Ig-like
- Immunoglobulin domain
- Kinase
- Limb-girdle muscular dystrophy
- Magnesium
- Nucleotide-binding
- Nucleus
- Obscurin
- Obsl1
- Phosphoprotein
- Polymorphism
- Serine/threonine-protein kinase
- Titin
- Transferase