2edu: Difference between revisions
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'''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'' | ||
Revision as of 15:08, 21 February 2008
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Solution structure of RSGI RUH-070, a C-terminal domain of kinesin-like protein KIF22 from human cDNA
Disease
Known diseases associated with this structure: Bart-Pumphrey syndrome OMIM:[121011], Deafness, autosomal dominant 3 OMIM:[121011], Deafness, autosomal recessive 1 OMIM:[121011], Hystrix-like ichthyosis with deafness OMIM:[121011], Keratitis-ichthyosis-deafness syndrome OMIM:[121011], Keratoderma, palmoplantar, with deafness OMIM:[121011], Vohwinkel syndrome OMIM:[121011]
About this Structure
2EDU 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 17:08:57 2008
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Single protein
- Abe, T.
- Hayashi, F.
- Hirota, H.
- RSGI, RIKEN Structural Genomics/Proteomics Initiative.
- Yokoyama, S.
- Helix turn helix motif
- Kinesin
- Kinesin-like 4
- Kinesin-like dna binding domain
- National project on protein structural and functional analyses
- Nppsfa
- Riken structural genomics/proteomics initiative
- Rsgi
- Structural genomics
- Transport protein
