2edu: Difference between revisions
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caption="2edu" /> | caption="2edu" /> | ||
'''Solution structure of RSGI RUH-070, a C-terminal domain of kinesin-like protein KIF22 from human cDNA'''<br /> | '''Solution structure of RSGI RUH-070, a C-terminal domain of kinesin-like protein KIF22 from human cDNA'''<br /> | ||
==Disease== | |||
Known diseases associated with this structure: Bart-Pumphrey syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Deafness, autosomal dominant 3 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Deafness, autosomal recessive 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Hystrix-like ichthyosis with deafness OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Keratitis-ichthyosis-deafness syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Keratoderma, palmoplantar, with deafness OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]], Vohwinkel syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011 121011]] | |||
==About this Structure== | ==About this Structure== | ||
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[[Category: Hayashi, F.]] | [[Category: Hayashi, F.]] | ||
[[Category: Hirota, H.]] | [[Category: Hirota, H.]] | ||
[[Category: RSGI, RIKEN | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] | ||
[[Category: Yokoyama, S.]] | [[Category: Yokoyama, S.]] | ||
[[Category: helix turn helix motif]] | [[Category: helix turn helix motif]] | ||
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[[Category: transport protein]] | [[Category: transport protein]] | ||
''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 17:08:57 2008'' | ||
