2css
From Proteopedia
(Difference between revisions)
| Line 3: | Line 3: | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2css]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CSS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2CSS FirstGlance]. <br> | <table><tr><td colspan='2'>[[2css]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CSS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2CSS FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">KAZUSA cDNA hg01396 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> | + | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">KAZUSA cDNA hg01396 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> |
| - | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2css FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2css OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2css RCSB], [http://www.ebi.ac.uk/pdbsum/2css PDBsum], [http://www.topsan.org/Proteins/RSGI/2css TOPSAN]</span></td></tr> | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2css FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2css OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2css RCSB], [http://www.ebi.ac.uk/pdbsum/2css PDBsum], [http://www.topsan.org/Proteins/RSGI/2css TOPSAN]</span></td></tr> |
| - | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/RIMS1_HUMAN RIMS1_HUMAN]] Defects in RIMS1 may be a cause of cone-rod dystrophy type 7 (CORD7) [MIM:[http://omim.org/entry/603649 603649]]. CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa.<ref>PMID:12659814</ref> | [[http://www.uniprot.org/uniprot/RIMS1_HUMAN RIMS1_HUMAN]] Defects in RIMS1 may be a cause of cone-rod dystrophy type 7 (CORD7) [MIM:[http://omim.org/entry/603649 603649]]. CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa.<ref>PMID:12659814</ref> | ||
| Line 25: | Line 25: | ||
</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Hayashi, F | + | [[Category: Hayashi, F]] |
| - | [[Category: Inoue, K | + | [[Category: Inoue, K]] |
| - | [[Category: Qin, X R | + | [[Category: Qin, X R]] |
| - | [[Category: | + | [[Category: Structural genomic]] |
| - | [[Category: Yokoyama, S | + | [[Category: Yokoyama, S]] |
[[Category: Endocytosis-exocytosis complex]] | [[Category: Endocytosis-exocytosis complex]] | ||
[[Category: National project on protein structural and functional analyse]] | [[Category: National project on protein structural and functional analyse]] | ||
| Line 36: | Line 36: | ||
[[Category: Rab3-interacting molecule 1]] | [[Category: Rab3-interacting molecule 1]] | ||
[[Category: Regulating synaptic membrane exocytosis protein 1]] | [[Category: Regulating synaptic membrane exocytosis protein 1]] | ||
| - | [[Category: Riken structural genomics/proteomics initiative]] | ||
[[Category: Rim 1]] | [[Category: Rim 1]] | ||
[[Category: Rsgi]] | [[Category: Rsgi]] | ||
| - | [[Category: Structural genomic]] | ||
Revision as of 18:28, 15 January 2015
Solution structure of the PDZ domain of human KIAA0340 protein
| |||||||||||
Categories: Homo sapiens | Hayashi, F | Inoue, K | Qin, X R | Structural genomic | Yokoyama, S | Endocytosis-exocytosis complex | National project on protein structural and functional analyse | Nppsfa | Pdz domain | Rab3-interacting molecule 1 | Regulating synaptic membrane exocytosis protein 1 | Rim 1 | Rsgi
