1rg6
From Proteopedia
(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 11:51, 20 March 2008
| |||||||
| Gene: | p63 (Homo sapiens) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
Solution structure of the C-terminal domain of p63
Disease
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 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
