1l3k
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1l3k]] is a 1 chain structure with 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=1L3K OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1L3K FirstGlance]. <br> | <table><tr><td colspan='2'>[[1l3k]] is a 1 chain structure with 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=1L3K OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1L3K FirstGlance]. <br> | ||
| - | </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=1l3k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1l3k OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1l3k RCSB], [http://www.ebi.ac.uk/pdbsum/1l3k PDBsum]</span></td></tr> | + | </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=1l3k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1l3k OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1l3k RCSB], [http://www.ebi.ac.uk/pdbsum/1l3k PDBsum]</span></td></tr> |
| - | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/ROA1_HUMAN ROA1_HUMAN]] Amyotrophic lateral sclerosis;Inclusion body myopathy with Paget disease of bone and frontotemporal dementia. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref> | [[http://www.uniprot.org/uniprot/ROA1_HUMAN ROA1_HUMAN]] Amyotrophic lateral sclerosis;Inclusion body myopathy with Paget disease of bone and frontotemporal dementia. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:23455423</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Ding, J | + | [[Category: Ding, J]] |
| - | [[Category: Jiang, J | + | [[Category: Jiang, J]] |
| - | [[Category: Krainer, A R | + | [[Category: Krainer, A R]] |
| - | [[Category: Vitali, J | + | [[Category: Vitali, J]] |
| - | [[Category: Xu, R M | + | [[Category: Xu, R M]] |
| - | [[Category: Zhang, Y | + | [[Category: Zhang, Y]] |
[[Category: Nuclear protein hnrnp a1]] | [[Category: Nuclear protein hnrnp a1]] | ||
[[Category: Rna binding protein]] | [[Category: Rna binding protein]] | ||
Revision as of 16:27, 5 January 2015
UP1, THE TWO RNA-RECOGNITION MOTIF DOMAIN OF HNRNP A1
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