1rg6: Difference between revisions
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[[Image:1rg6.gif|left|200px]] | [[Image:1rg6.gif|left|200px]] | ||
'''Solution structure of the C-terminal domain of p63''' | {{Structure | ||
|PDB= 1rg6 |SIZE=350|CAPTION= <scene name='initialview01'>1rg6</scene> | |||
|SITE= | |||
|LIGAND= | |||
|ACTIVITY= | |||
|GENE= p63 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]) | |||
}} | |||
'''Solution structure of the C-terminal domain of p63''' | |||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
1RG6 is a [ | 1RG6 is a [[Single protein]] 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=1RG6 OCA]. | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: p73 sam-like domain]] | [[Category: p73 sam-like domain]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 13:51:09 2008'' | ||
Revision as of 14:51, 20 March 2008
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| Gene: | p63 (Homo sapiens) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Solution structure of the C-terminal domain of p63
DiseaseDisease
Known diseases associated with this structure: ADULT syndrome OMIM:[603273], Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 OMIM:[603273], Hay-Wells syndrome OMIM:[603273], Limb-mammary syndrome OMIM:[603273], Orofacial cleft 8 OMIM:[603273], Rapp-Hodgkin syndrome OMIM:[603273], Split-hand/foot malformation, type 4 OMIM:[603273]
About this StructureAbout this Structure
1RG6 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Mar 20 13:51:09 2008