1ufx: Difference between revisions
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[[Category: Ohara, O.]] | [[Category: Ohara, O.]] | ||
[[Category: Osanai, T.]] | [[Category: Osanai, T.]] | ||
[[Category: RSGI, RIKEN | [[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]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:24:03 2008'' |
Revision as of 16:24, 21 February 2008
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Solution structure of the third PDZ domain of human KIAA1526 protein
DiseaseDisease
Known diseases associated with this structure: Deafness, autosomal recessive 31 OMIM:[607928], Usher syndrome, type IID OMIM:[607928]
About this StructureAbout 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
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Aoki, M.
- Hirota, H.
- Inoue, M.
- Kigawa, T.
- Kikuno, R.
- Kobayashi, N.
- Koshiba, S.
- Matsuda, T.
- Matsuo, Y.
- Nagase, T.
- Nakayama, M.
- Ohara, O.
- Osanai, T.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Seki, E.
- Shirouzu, M.
- Tanaka, A.
- Terada, T.
- Tochio, N.
- Yabuki, T.
- Yokoyama, S.
- Yoshida, M.
- Pdz domain
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomics