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1x5n
From Proteopedia
(New page: 200px<br /> <applet load="1x5n" size="450" color="white" frame="true" align="right" spinBox="true" caption="1x5n" /> '''Solution structure of the second PDZ domain...) |
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| - | [[Image:1x5n.gif|left|200px]]<br /> | + | [[Image:1x5n.gif|left|200px]]<br /><applet load="1x5n" size="350" color="white" frame="true" align="right" spinBox="true" |
| - | <applet load="1x5n" size=" | + | |
caption="1x5n" /> | caption="1x5n" /> | ||
'''Solution structure of the second PDZ domain of harmonin protein'''<br /> | '''Solution structure of the second PDZ domain of harmonin protein'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1X5N is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http:// | + | 1X5N is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1X5N OCA]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Hayashi, F.]] | [[Category: Hayashi, F.]] | ||
| - | [[Category: Qin, X | + | [[Category: Qin, X R.]] |
| - | [[Category: RSGI, RIKEN | + | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] |
[[Category: Yokoyama, S.]] | [[Category: Yokoyama, S.]] | ||
[[Category: antigen ny-co-38/ny-co-37]] | [[Category: antigen ny-co-38/ny-co-37]] | ||
| Line 27: | Line 26: | ||
[[Category: usher syndrome 1c protein]] | [[Category: usher syndrome 1c protein]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:51:16 2008'' |
Revision as of 13:51, 21 February 2008
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Solution structure of the second PDZ domain of harmonin protein
Disease
Known diseases associated with this structure: Deafness, autosomal recessive 18 OMIM:[605242], Usher syndrome, type 1C OMIM:[605242]
About this Structure
1X5N 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 15:51:16 2008
Categories: Homo sapiens | Single protein | Hayashi, F. | Qin, X R. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Yokoyama, S. | Antigen ny-co-38/ny-co-37 | Autoimmune enteropathy-related antigen aie-75 | Harmonin | National project on protein structural and functional analyses | Nppsfa | Pdz domain | Pdz-73 protein | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics | Usher syndrome 1c protein
