2cur

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|PDB= 2cur |SIZE=350|CAPTION= <scene name='initialview01'>2cur</scene>
|PDB= 2cur |SIZE=350|CAPTION= <scene name='initialview01'>2cur</scene>
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=ZN:ZINC ION'>ZN</scene>
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|LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
|ACTIVITY=
|ACTIVITY=
|GENE= FHL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= FHL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
 +
|DOMAIN=
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2cur FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cur OCA], [http://www.ebi.ac.uk/pdbsum/2cur PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2cur RCSB]</span>
}}
}}
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==Disease==
==Disease==
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Known diseases associated with this structure: Hemophagocytic lymphohistiocytosis, familial OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=267700 267700]], Myopathy, X-linked, with postural muscle atrophy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]], Scapuloperoneal myopathy, X-linked dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]]
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Known disease associated with this structure: Hemophagocytic lymphohistiocytosis, familial OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=267700 267700]], Myopathy, X-linked, with postural muscle atrophy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]], Scapuloperoneal myopathy, X-linked dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300163 300163]]
==About this Structure==
==About this Structure==
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[[Category: Tomizawa, T.]]
[[Category: Tomizawa, T.]]
[[Category: Yokoyama, S.]]
[[Category: Yokoyama, S.]]
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[[Category: ZN]]
 
[[Category: four and a half lim domains protein 1]]
[[Category: four and a half lim domains protein 1]]
[[Category: lim]]
[[Category: lim]]
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[[Category: structural genomic]]
[[Category: structural genomic]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:20:01 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:26:39 2008''

Revision as of 23:26, 30 March 2008

Image:2cur.gif


PDB ID 2cur

Drag the structure with the mouse to rotate
Ligands:
Gene: FHL1 (Homo sapiens)
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Solution structure of Skeletal muscle LIM-protein 1


Disease

Known disease associated with this structure: Hemophagocytic lymphohistiocytosis, familial OMIM:[267700], Myopathy, X-linked, with postural muscle atrophy OMIM:[300163], Scapuloperoneal myopathy, X-linked dominant OMIM:[300163]

About this Structure

2CUR is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Mon Mar 31 02:26:39 2008

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