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8CHP

The FK1 domain of FKBP51 in complex with (1S,5S,6R)-10-((S)-(3,5-dichlorophenyl)sulfinyl)-3-(pyridin-2-ylmethyl)-5-vinyl-3,10-diazabicyclo[4.3.1]decan-2-one

Summary for 8CHP
Entry DOI10.2210/pdb8chp/pdb
DescriptorPeptidyl-prolyl cis-trans isomerase FKBP5, (1~{S},5~{S},6~{R})-10-[3,5-bis(chloranyl)phenyl]sulfinyl-5-ethenyl-3-(pyridin-2-ylmethyl)-3,10-diazabicyclo[4.3.1]decan-2-one (3 entities in total)
Functional Keywordsfkbp51, inhibitor, isomerase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight14468.43
Authors
Meyners, C.,Purder, P.L.,Hausch, F. (deposition date: 2023-02-08, release date: 2023-09-06, Last modification date: 2023-10-11)
Primary citationPurder, P.L.,Meyners, C.,Sugiarto, W.O.,Kolos, J.,Lohr, F.,Gebel, J.,Nehls, T.,Dotsch, V.,Lermyte, F.,Hausch, F.
Deconstructing Protein Binding of Sulfonamides and Sulfonamide Analogues.
Jacs Au, 3:2478-2486, 2023
Cited by
PubMed Abstract: Sulfonamides are one of the most important pharmacophores in medicinal chemistry, and sulfonamide analogues have gained substantial interest in recent years. However, the protein interactions of sulfonamides and especially of their analogues are underexplored. Using FKBP12 as a model system, we describe the synthesis of optically pure sulfenamide, sulfinamide, and sulfonimidamide analogues of a well characterized sulfonamide ligand. This allowed us to precisely determine the binding contributions of each sulfonamide oxygen atom and the consequences of nitrogen replacements. We also present high-resolution cocrystal structures of sulfonamide analogues buried in the pocket of a protein target. This revealed intimate contacts with the protein including an unprecedented hydrogen bond acceptor of sulfonimidamides. The use of sulfonamide analogues enabled new exit vectors that allowed remodeling of a subpocket in FKBP12. Our results illuminate the protein interaction potential of sulfonamides/sulfonamide analogues and will aid in their rational design.
PubMed: 37772190
DOI: 10.1021/jacsau.3c00241
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1 Å)
Structure validation

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数据于2024-11-06公开中

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