1u1k: Difference between revisions

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1u1k]] is a 2 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=1U1K OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1U1K FirstGlance]. <br>
<table><tr><td colspan='2'>[[1u1k]] is a 2 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=1U1K OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1U1K FirstGlance]. <br>
</td></tr><tr><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=7DA:7-DEAZA-2-DEOXYADENOSINE-5-MONOPHOSPHATE'>7DA</scene></td></tr>
</td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=7DA:7-DEAZA-2-DEOXYADENOSINE-5-MONOPHOSPHATE'>7DA</scene></td></tr>
<tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2up1|2up1]], [[1pgz|1pgz]], [[1po6|1po6]], [[1u1l|1u1l]], [[1u1m|1u1m]], [[1u1n|1u1n]], [[1u1o|1u1o]], [[1u1p|1u1p]], [[1u1q|1u1q]], [[1u1r|1u1r]]</td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2up1|2up1]], [[1pgz|1pgz]], [[1po6|1po6]], [[1u1l|1u1l]], [[1u1m|1u1m]], [[1u1n|1u1n]], [[1u1o|1u1o]], [[1u1p|1u1p]], [[1u1q|1u1q]], [[1u1r|1u1r]]</td></tr>
<tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">HNRPA1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">HNRPA1 ([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=1u1k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1u1k OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1u1k RCSB], [http://www.ebi.ac.uk/pdbsum/1u1k PDBsum]</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=1u1k FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1u1k OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1u1k RCSB], [http://www.ebi.ac.uk/pdbsum/1u1k 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: Myers, J C.]]
[[Category: Myers, J C]]
[[Category: Shamoo, Y.]]
[[Category: Shamoo, Y]]
[[Category: 7-deaza-adenine]]
[[Category: 7-deaza-adenine]]
[[Category: 7da]]
[[Category: Hnrnp a1]]
[[Category: Hnrnp a1]]
[[Category: Htr]]
[[Category: Htr]]

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