1k1b

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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[1k1b]] 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=1K1B OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1K1B FirstGlance]. <br>
<table><tr><td colspan='2'>[[1k1b]] 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=1K1B OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1K1B FirstGlance]. <br>
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</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1k1a|1k1a]]</td></tr>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1k1a|1k1a]]</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=1k1b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1k1b OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1k1b RCSB], [http://www.ebi.ac.uk/pdbsum/1k1b 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=1k1b FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1k1b OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1k1b RCSB], [http://www.ebi.ac.uk/pdbsum/1k1b PDBsum]</span></td></tr>
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<table>
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</table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/BCL3_HUMAN BCL3_HUMAN]] Note=A chromosomal aberration involving BCL3 may be a cause of B-cell chronic lymphocytic leukemia (B-CLL). Translocation t(14;19)(q32;q13.1) with immunoglobulin gene regions.
[[http://www.uniprot.org/uniprot/BCL3_HUMAN BCL3_HUMAN]] Note=A chromosomal aberration involving BCL3 may be a cause of B-cell chronic lymphocytic leukemia (B-CLL). Translocation t(14;19)(q32;q13.1) with immunoglobulin gene regions.
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</StructureSection>
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Cramer, P.]]
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[[Category: Cramer, P]]
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[[Category: Michel, F.]]
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[[Category: Michel, F]]
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[[Category: Mueller, C W.]]
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[[Category: Mueller, C W]]
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[[Category: Petosa, C.]]
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[[Category: Petosa, C]]
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[[Category: Siebenlist, U.]]
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[[Category: Siebenlist, U]]
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[[Category: Soler-Lopez, M.]]
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[[Category: Soler-Lopez, M]]
[[Category: Bcl-3]]
[[Category: Bcl-3]]
[[Category: Ikappab protein]]
[[Category: Ikappab protein]]
[[Category: Nf-kappab transcription factor]]
[[Category: Nf-kappab transcription factor]]
[[Category: Transcription]]
[[Category: Transcription]]

Revision as of 15:39, 5 January 2015

Crystal structure of the ankyrin repeat domain of Bcl-3: a unique member of the IkappaB protein family

1k1b, resolution 1.90Å

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