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6M4W

Crystal structure of MBP fused split FKBP-FRB T2098L mutant in complex with rapamycin

Summary for 6M4W
Entry DOI10.2210/pdb6m4w/pdb
Related PRD IDPRD_900001
Descriptorchimera of Maltose/maltodextrin-binding periplasmic protein and Peptidyl-prolyl cis-trans isomerase FKBP1A, Peptidyl-prolyl cis-trans isomerase FKBP1A, Serine/threonine-protein kinase mTOR, ... (7 entities in total)
Functional Keywordsrapamycin, complex, kinase, isomerase
Biological sourceEscherichia coli K-12
More
Total number of polymer chains9
Total formula weight195887.56
Authors
Kikuchi, M.,Wu, D.,Inoue, T.,Umehara, T. (deposition date: 2020-03-09, release date: 2020-08-26, Last modification date: 2023-11-29)
Primary citationWu, H.D.,Kikuchi, M.,Dagliyan, O.,Aragaki, A.K.,Nakamura, H.,Dokholyan, N.V.,Umehara, T.,Inoue, T.
Rational design and implementation of a chemically inducible heterotrimerization system.
Nat.Methods, 17:928-936, 2020
Cited by
PubMed Abstract: Chemically inducible dimerization (CID) uses a small molecule to induce binding of two different proteins. CID tools such as the FK506-binding protein-FKBP-rapamycin-binding- (FKBP-FRB)-rapamycin system have been widely used to probe molecular events inside and outside cells. While various CID tools are available, chemically inducible trimerization (CIT) does not exist, due to inherent challenges in designing a chemical that simultaneously binds three proteins with high affinity and specificity. Here, we developed CIT by rationally splitting FRB and FKBP. Cellular and structural datasets showed efficient trimerization of split pairs of FRB or FKBP with full-length FKBP or FRB, respectively, by rapamycin. CIT rapidly induced tri-organellar junctions and perturbed intended membrane lipids exclusively at select membrane contact sites. By conferring one additional condition to what is achievable with CID, CIT expands the types of manipulation in single live cells to address cell biology questions otherwise intractable and engineer cell functions for future synthetic biology applications.
PubMed: 32747768
DOI: 10.1038/s41592-020-0913-x
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.11 Å)
Structure validation

229380

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