1qgp: Difference between revisions
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1qgp]] 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=1QGP OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1QGP FirstGlance]. <br> | <table><tr><td colspan='2'>[[1qgp]] 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=1QGP OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1QGP 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=1qgp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1qgp OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1qgp RCSB], [http://www.ebi.ac.uk/pdbsum/1qgp 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=1qgp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1qgp OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1qgp RCSB], [http://www.ebi.ac.uk/pdbsum/1qgp PDBsum]</span></td></tr> | ||
<table> | </table> | ||
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/DSRAD_HUMAN DSRAD_HUMAN]] Defects in ADAR are a cause of dyschromatosis symmetrical hereditaria (DSH) [MIM:[http://omim.org/entry/127400 127400]]; also known as reticulate acropigmentation of Dohi. DSH is a pigmentary genodermatosis of autosomal dominant inheritance characterized by a mixture of hyperpigmented and hypopigmented macules distributed on the dorsal parts of the hands and feet.<ref>PMID:12916015</ref> <ref>PMID:15146470</ref> <ref>PMID:15659327</ref> | [[http://www.uniprot.org/uniprot/DSRAD_HUMAN DSRAD_HUMAN]] Defects in ADAR are a cause of dyschromatosis symmetrical hereditaria (DSH) [MIM:[http://omim.org/entry/127400 127400]]; also known as reticulate acropigmentation of Dohi. DSH is a pigmentary genodermatosis of autosomal dominant inheritance characterized by a mixture of hyperpigmented and hypopigmented macules distributed on the dorsal parts of the hands and feet.<ref>PMID:12916015</ref> <ref>PMID:15146470</ref> <ref>PMID:15659327</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Herbert, A | [[Category: Herbert, A]] | ||
[[Category: Kuehne, R | [[Category: Kuehne, R]] | ||
[[Category: Lowenhaupt, K | [[Category: Lowenhaupt, K]] | ||
[[Category: Oschkinat, H | [[Category: Oschkinat, H]] | ||
[[Category: Rich, A | [[Category: Rich, A]] | ||
[[Category: Schade, M | [[Category: Schade, M]] | ||
[[Category: Schmieder, P | [[Category: Schmieder, P]] | ||
[[Category: Turner, C J | [[Category: Turner, C J]] | ||
[[Category: Adar1]] | [[Category: Adar1]] | ||
[[Category: Helix- turn-helix]] | [[Category: Helix- turn-helix]] | ||
