1z9e

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1z9e]] 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=1Z9E OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1Z9E FirstGlance]. <br>
<table><tr><td colspan='2'>[[1z9e]] 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=1Z9E OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1Z9E FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">PSIP1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr>
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</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">PSIP1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr>
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<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=1z9e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1z9e OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1z9e RCSB], [http://www.ebi.ac.uk/pdbsum/1z9e PDBsum]</span></td></tr>
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<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=1z9e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1z9e OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1z9e RCSB], [http://www.ebi.ac.uk/pdbsum/1z9e PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/PSIP1_HUMAN PSIP1_HUMAN]] Note=A chromosomal aberration involving PSIP1 is associated with pediatric acute myeloid leukemia (AML) with intermediate characteristics between M2-M3 French-American-British (FAB) subtypes. Translocation t(9;11)(p22;p15) with NUP98. The chimeric transcript is an in-frame fusion of NUP98 exon 8 to PSIP1/LEDGF exon 4.
[[http://www.uniprot.org/uniprot/PSIP1_HUMAN PSIP1_HUMAN]] Note=A chromosomal aberration involving PSIP1 is associated with pediatric acute myeloid leukemia (AML) with intermediate characteristics between M2-M3 French-American-British (FAB) subtypes. Translocation t(9;11)(p22;p15) with NUP98. The chimeric transcript is an in-frame fusion of NUP98 exon 8 to PSIP1/LEDGF exon 4.
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Cherepanov, P.]]
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[[Category: Cherepanov, P]]
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[[Category: Engelman, A.]]
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[[Category: Engelman, A]]
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[[Category: Maertens, G.]]
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[[Category: Maertens, G]]
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[[Category: Rahman, S.]]
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[[Category: Rahman, S]]
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[[Category: Sun, Z Y.J.]]
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[[Category: Sun, Z Y.J]]
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[[Category: Wagner, G.]]
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[[Category: Wagner, G]]
[[Category: Heat repeat-like]]
[[Category: Heat repeat-like]]
[[Category: Ledgf]]
[[Category: Ledgf]]
[[Category: Protein binding-transcription complex]]
[[Category: Protein binding-transcription complex]]

Revision as of 10:27, 8 January 2015

Solution structure of the HIV-1 integrase-binding domain in LEDGF/p75

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