2b9a: Difference between revisions
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<StructureSection load='2b9a' size='340' side='right' caption='[[2b9a]], [[Resolution|resolution]] 1.54Å' scene=''> | <StructureSection load='2b9a' size='340' side='right' caption='[[2b9a]], [[Resolution|resolution]] 1.54Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2b9a]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B9A OCA]. <br> | <table><tr><td colspan='2'>[[2b9a]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2B9A OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2B9A FirstGlance]. <br> | ||
</td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FBC:3,5-DIFLUOROBIPHENYL-4-CARBOXYLIC+ACID'>FBC</scene><br> | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=FBC:3,5-DIFLUOROBIPHENYL-4-CARBOXYLIC+ACID'>FBC</scene><br> | ||
<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=2b9a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2b9a OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2b9a RCSB], [http://www.ebi.ac.uk/pdbsum/2b9a PDBsum]</span></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=2b9a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2b9a OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2b9a RCSB], [http://www.ebi.ac.uk/pdbsum/2b9a PDBsum]</span></td></tr> | ||
<table> | <table> | ||
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Diflunisal analogues stabilize the native state of transthyretin. Potent inhibition of amyloidogenesis.,Adamski-Werner SL, Palaninathan SK, Sacchettini JC, Kelly JW J Med Chem. 2004 Jan 15;47(2):355-74. PMID:14711308<ref>PMID:14711308</ref> | Diflunisal analogues stabilize the native state of transthyretin. Potent inhibition of amyloidogenesis.,Adamski-Werner SL, Palaninathan SK, Sacchettini JC, Kelly JW J Med Chem. 2004 Jan 15;47(2):355-74. PMID:14711308<ref>PMID:14711308</ref> | ||
From | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
==See Also== | |||
*[[Transthyretin|Transthyretin]] | |||
== References == | == References == | ||
<references/> | <references/> | ||