2k3t
From Proteopedia
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| + | {{STRUCTURE_2k3t| PDB=2k3t | SCENE= }} | ||
| - | + | ===Solution Structure of IG-Like Domain 23 from Human Filamin A=== | |
| - | Description: Solution Structure of IG-Like Domain 23 from Human Filamin A | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19293932}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19293932 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19293932}} | ||
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| + | ==About this Structure== | ||
| + | 2K3T 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=2K3T OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19293932</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Heikkinen, O K.]] | ||
| + | [[Category: Kilpelainen, I.]] | ||
| + | [[Category: Kupiainen, O.]] | ||
| + | [[Category: Ylanne, J.]] | ||
| + | [[Category: Acetylation]] | ||
| + | [[Category: Actin-binding]] | ||
| + | [[Category: Cytoplasm]] | ||
| + | [[Category: Cytoskeleton]] | ||
| + | [[Category: Disease mutation]] | ||
| + | [[Category: Filamin some]] | ||
| + | [[Category: Ig-like]] | ||
| + | [[Category: Immunoglobulin]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Structural protein]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Apr 2 15:29:24 2009'' | ||
Revision as of 12:29, 2 April 2009
Solution Structure of IG-Like Domain 23 from Human Filamin A
Template:ABSTRACT PUBMED 19293932
About this Structure
2K3T is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Nakamura F, Heikkinen O, Pentikainen OT, Osborn TM, Kasza KE, Weitz DA, Kupiainen O, Permi P, Kilpelainen I, Ylanne J, Hartwig JH, Stossel TP. Molecular basis of filamin A-FilGAP interaction and its impairment in congenital disorders associated with filamin A mutations. PLoS ONE. 2009;4(3):e4928. Epub 2009 Mar 18. PMID:19293932 doi:10.1371/journal.pone.0004928
Page seeded by OCA on Thu Apr 2 15:29:24 2009
