4bwq

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<StructureSection load='4bwq' size='340' side='right' caption='[[4bwq]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
<StructureSection load='4bwq' size='340' side='right' caption='[[4bwq]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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[[4bwq]] is a 8 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BWQ OCA]. <br>
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<table><tr><td colspan='2'>[[4bwq]] is a 8 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4BWQ OCA]. <br>
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<b>[[Related_structure|Related:]]</b> [[4bws|4bws]]<br>
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</td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4bws|4bws]]</td></tr>
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<b>Activity:</b> <span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span><br>
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<tr><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Glucokinase Glucokinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.1.2 2.7.1.2] </span></td></tr>
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<b>Resources:</b> <span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4bwq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bwq OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4bwq RCSB], [http://www.ebi.ac.uk/pdbsum/4bwq PDBsum]</span><br>
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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=4bwq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4bwq OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4bwq RCSB], [http://www.ebi.ac.uk/pdbsum/4bwq PDBsum]</span></td></tr>
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<table>
== Disease ==
== Disease ==
[[http://www.uniprot.org/uniprot/PQBP1_HUMAN PQBP1_HUMAN]] X-linked intellectual deficit, Sutherland-Haan type;X-linked intellectual deficit, Golabi-Ito-Hall type;X-linked intellectual deficit, Porteous type;Hamel cerebro-palato-cardiac syndrome. The disease is caused by mutations affecting the gene represented in this entry.
[[http://www.uniprot.org/uniprot/PQBP1_HUMAN PQBP1_HUMAN]] X-linked intellectual deficit, Sutherland-Haan type;X-linked intellectual deficit, Golabi-Ito-Hall type;X-linked intellectual deficit, Porteous type;Hamel cerebro-palato-cardiac syndrome. The disease is caused by mutations affecting the gene represented in this entry.

Revision as of 09:19, 1 May 2014

Crystal structure of U5-15kD in a complex with PQBP1

4bwq, resolution 2.10Å

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