8CHQ
The FK1 domain of FKBP51 in complex with (1S,5S,6R)-10-((S)-3,5-dichloro-N-methylphenylsulfonimidoyl)-3-(pyridin-2-ylmethyl)-5-vinyl-3,10-diazabicyclo[4.3.1]decan-2-one
Summary for 8CHQ
Entry DOI | 10.2210/pdb8chq/pdb |
Descriptor | Peptidyl-prolyl cis-trans isomerase FKBP5, (1S,5S,6R)-10-[S-[3,5-bis(chloranyl)phenyl]-N-methyl-sulfonimidoyl]-5-ethenyl-3-(pyridin-2-ylmethyl)-3,10-diazabicyclo[4.3.1]decan-2-one (3 entities in total) |
Functional Keywords | fkbp51, inhibitor, isomerase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 14497.48 |
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 citation | Purder, 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: 37772190DOI: 10.1021/jacsau.3c00241 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.01 Å) |
Structure validation
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