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1ufx

From Proteopedia

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[[Category: Ohara, O.]]
[[Category: Ohara, O.]]
[[Category: Osanai, T.]]
[[Category: Osanai, T.]]
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[[Category: RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative.]]
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[[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]]
[[Category: Seki, E.]]
[[Category: Seki, E.]]
[[Category: Shirouzu, M.]]
[[Category: Shirouzu, M.]]
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[[Category: structural genomics]]
[[Category: structural genomics]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:01:44 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:24:03 2008''

Revision as of 13:24, 21 February 2008


1ufx

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Solution structure of the third PDZ domain of human KIAA1526 protein

Disease

Known diseases associated with this structure: Deafness, autosomal recessive 31 OMIM:[607928], Usher syndrome, type IID OMIM:[607928]

About this Structure

1UFX is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Page seeded by OCA on Thu Feb 21 15:24:03 2008

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