2edu
From Proteopedia
| Line 2: | Line 2: | ||
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== | ||
| Line 10: | Line 13: | ||
[[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]] | ||
| Line 23: | Line 26: | ||
[[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
|
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
Categories: 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
