6i1z

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'''Unreleased structure'''
 
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The entry 6i1z is ON HOLD until Paper Publication
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==Outward facing structure of apo CST==
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<StructureSection load='6i1z' size='340' side='right'caption='[[6i1z]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6i1z]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6I1Z OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6I1Z FirstGlance]. <br>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6i1r|6i1r]]</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=6i1z FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6i1z OCA], [http://pdbe.org/6i1z PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6i1z RCSB], [http://www.ebi.ac.uk/pdbsum/6i1z PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6i1z ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The decoration of secretory glycoproteins and glycolipids with sialic acid is critical to many physiological and pathological processes. Sialyation is dependent on a continuous supply of sialic acid into Golgi organelles in the form of CMP-sialic acid. Translocation of CMP-sialic acid into Golgi is carried out by the CMP-sialic acid transporter (CST). Mutations in human CST are linked to glycosylation disorders, and CST is important for glycopathway engineering, as it is critical for sialyation efficiency of therapeutic glycoproteins. The mechanism of how CMP-sialic acid is recognized and translocated across Golgi membranes in exchange for CMP is poorly understood. Here we have determined the crystal structure of a Zea mays CST in complex with CMP. We conclude that the specificity of CST for CMP-sialic acid is established by the recognition of the nucleotide CMP to such an extent that they are mechanistically capable of both passive and coupled antiporter activity.
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Authors:
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Structural basis for the delivery of activated sialic acid into Golgi for sialyation.,Nji E, Gulati A, Qureshi AA, Coincon M, Drew D Nat Struct Mol Biol. 2019 May 27. pii: 10.1038/s41594-019-0225-y. doi:, 10.1038/s41594-019-0225-y. PMID:31133698<ref>PMID:31133698</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 6i1z" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Drew, D]]
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[[Category: Gulati, A]]
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[[Category: Nji, E]]
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[[Category: Qureshi, A A]]
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[[Category: Cmp-sialic acid transporter]]
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[[Category: Membrane protein]]
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[[Category: Nucleotide sugar transporter]]
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[[Category: Secondary active transporter]]
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[[Category: Slc35a1]]

Revision as of 22:46, 5 June 2019

Outward facing structure of apo CST

PDB ID 6i1z

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