5i66
From Proteopedia
(Difference between revisions)
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- | '''Unreleased structure''' | ||
- | + | ==X-ray structure of the Fab fragment of 8B6, a murine monoclonal antibody specific for the human serotonin transporter== | |
+ | <StructureSection load='5i66' size='340' side='right' caption='[[5i66]], [[Resolution|resolution]] 1.62Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[5i66]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5I66 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5I66 FirstGlance]. <br> | ||
+ | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5i6x|5i6x]], [[5i6z|5i6z]], [[5i71|5i71]], [[5i73|5i73]], [[5i74|5i74]], [[5i75|5i75]]</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=5i66 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5i66 OCA], [http://pdbe.org/5i66 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5i66 RCSB], [http://www.ebi.ac.uk/pdbsum/5i66 PDBsum]</span></td></tr> | ||
+ | </table> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | The serotonin transporter (SERT) terminates serotonergic signalling through the sodium- and chloride-dependent reuptake of neurotransmitter into presynaptic neurons. SERT is a target for antidepressant and psychostimulant drugs, which block reuptake and prolong neurotransmitter signalling. Here we report X-ray crystallographic structures of human SERT at 3.15 A resolution bound to the antidepressants (S)-citalopram or paroxetine. Antidepressants lock SERT in an outward-open conformation by lodging in the central binding site, located between transmembrane helices 1, 3, 6, 8 and 10, directly blocking serotonin binding. We further identify the location of an allosteric site in the complex as residing at the periphery of the extracellular vestibule, interposed between extracellular loops 4 and 6 and transmembrane helices 1, 6, 10 and 11. Occupancy of the allosteric site sterically hinders ligand unbinding from the central site, providing an explanation for the action of (S)-citalopram as an allosteric ligand. These structures define the mechanism of antidepressant action in SERT, and provide blueprints for future drug design. | ||
- | + | X-ray structures and mechanism of the human serotonin transporter.,Coleman JA, Green EM, Gouaux E Nature. 2016 Apr 21;532(7599):334-9. doi: 10.1038/nature17629. Epub 2016 Apr 6. PMID:27049939<ref>PMID:27049939</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | [[Category: | + | </div> |
+ | <div class="pdbe-citations 5i66" style="background-color:#fffaf0;"></div> | ||
+ | == References == | ||
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Coleman, J A]] | ||
[[Category: Gouaux, E]] | [[Category: Gouaux, E]] | ||
- | [[Category: Green, E | + | [[Category: Green, E M]] |
- | [[Category: | + | [[Category: Immune system]] |
+ | [[Category: Immunoglobulin fold]] |
Revision as of 17:37, 10 May 2016
X-ray structure of the Fab fragment of 8B6, a murine monoclonal antibody specific for the human serotonin transporter
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