21fk: Difference between revisions
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==Cryo-EM structure of DddT G101D in substrate-free inward open conformation== | |||
<StructureSection load='21fk' size='340' side='right'caption='[[21fk]], [[Resolution|resolution]] 3.29Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[21fk]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Psychrobacter_sp._D2 Psychrobacter sp. D2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=21FK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=21FK FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.29Å</td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=21fk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=21fk OCA], [https://pdbe.org/21fk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=21fk RCSB], [https://www.ebi.ac.uk/pdbsum/21fk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=21fk ProSAT]</span></td></tr> | |||
</table> | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Dimethylsulfoniopropionate (DMSP) is a ubiquitous marine organosulfur compound central to microbial stress responses, chemotaxis, and nutrient cycling. Its catabolism produces dimethylsulfide (DMS), a climate-active gas, and plays a key role in the global sulfur cycle. However, the molecular basis of DMSP import, underpinning its microbial metabolism, remains poorly understood. Here, we identify and characterize the BCCT-family transporter DddT from Psychrobacter sp. D2, a marine gamma-proteobacterium that utilizes DMSP as a carbon source. DddT is essential for DMSP uptake and functions as a Na(+)-coupled symporter driven by the transmembrane sodium gradient. Using cryo-electron microscopy, we determined DddT structures in multiple conformational states, revealing its Na(+)-dependent transport mechanism involving two sodium ions, one coordinated by a previously uncharacterized binding site. Sequence analysis shows that DddT-like proteins with conserved sodium-binding features are widespread in marine bacteria, suggesting this Na(+)-coupled transport mechanism represents a broadly conserved feature of the BCCT family. Our findings provide mechanistic insights into sodium-driven substrate uptake and marine sulfur cycling. | |||
Structural insights into bacterial dimethylsulfoniopropionate import by BCCT-family transporters.,Zhang YZ, Zhu WJ, Li K, Ding HT, Hattori M, Liu S, Ge C, Qin QL, Teng ZJ, Liu NH, Cao HY, Li CY, Chen XL, Shen QT, Todd JD, Liu LN, Wang P EMBO J. 2026 May 8. doi: 10.1038/s44318-026-00798-w. PMID:42104083<ref>PMID:42104083</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
[[Category: | </div> | ||
<div class="pdbe-citations 21fk" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Large Structures]] | |||
[[Category: Psychrobacter sp. D2]] | |||
[[Category: Wang P]] | |||
[[Category: Zhu WJ]] | |||
Latest revision as of 11:23, 24 May 2026
Cryo-EM structure of DddT G101D in substrate-free inward open conformation
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