1emo: Difference between revisions

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|PDB= 1emo |SIZE=350|CAPTION= <scene name='initialview01'>1emo</scene>
|PDB= 1emo |SIZE=350|CAPTION= <scene name='initialview01'>1emo</scene>
|SITE= <scene name='pdbsite=CA1:Ca+Binding+Site+For+Egf-Like+Domain+32'>CA1</scene> and <scene name='pdbsite=CA2:Ca+Binding+Site+For+Egf-Like+Domain+33'>CA2</scene>
|SITE= <scene name='pdbsite=CA1:Ca+Binding+Site+For+Egf-Like+Domain+32'>CA1</scene> and <scene name='pdbsite=CA2:Ca+Binding+Site+For+Egf-Like+Domain+33'>CA2</scene>
|LIGAND= <scene name='pdbligand=CA:CALCIUM ION'>CA</scene>
|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>
|ACTIVITY=  
|ACTIVITY=  
|GENE= FBN1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= FBN1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=[[1emn|1EMN]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1emo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1emo OCA], [http://www.ebi.ac.uk/pdbsum/1emo PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1emo RCSB]</span>
}}
}}


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==Disease==
==Disease==
Known diseases associated with this structure: Aortic aneurysm, ascending, and dissection OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Ectopia lentis, familial OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], MASS syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Marfan syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Shprintzen-Goldberg syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Weill-Marchesani syndrome, dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]]
Known disease associated with this structure: Aortic aneurysm, ascending, and dissection OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Ectopia lentis, familial OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], MASS syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Marfan syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Shprintzen-Goldberg syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]], Weill-Marchesani syndrome, dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797 134797]]


==About this Structure==
==About this Structure==
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[[Category: Downing, A K.]]
[[Category: Downing, A K.]]
[[Category: Handford, P A.]]
[[Category: Handford, P A.]]
[[Category: CA]]
[[Category: calcium-binding]]
[[Category: calcium-binding]]
[[Category: disease mutation]]
[[Category: disease mutation]]
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[[Category: signal]]
[[Category: signal]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:57:37 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:05:36 2008''
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