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8RIW

T2R-TTL-1-L01 complex

This is a non-PDB format compatible entry.
Summary for 8RIW
Entry DOI10.2210/pdb8riw/pdb
Related8RIV
DescriptorTubulin alpha-1B chain, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, (2-methyl-1~{H}-indol-5-yl) 3,4,5-trimethoxybenzenesulfonate, ... (14 entities in total)
Functional Keywordscell cycle, tubulin fold, cytoskeleton, microtubule
Biological sourceRattus norvegicus (Norway rat)
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Total number of polymer chains6
Total formula weight265543.49
Authors
Prota, A.E.P.,Boiarska, Z.,Homer, J.A.,Steinmetz, M.O.,Moses, J.E. (deposition date: 2023-12-19, release date: 2024-03-27)
Primary citationHomer, J.A.,Koelln, R.A.,Barrow, A.S.,Gialelis, T.L.,Boiarska, Z.,Steinohrt, N.S.,Lee, E.F.,Yang, W.H.,Johnson, R.M.,Chung, T.,Habowski, A.N.,Vishwakarma, D.S.,Bhunia, D.,Avanzi, C.,Moorhouse, A.D.,Jackson, M.,Tuveson, D.A.,Lyons, S.K.,Lukey, M.J.,Fairlie, W.D.,Haider, S.M.,Steinmetz, M.O.,Prota, A.E.,Moses, J.E.
Modular synthesis of functional libraries by accelerated SuFEx click chemistry.
Chem Sci, 15:3879-3892, 2024
Cited by
PubMed Abstract: Accelerated SuFEx Click Chemistry (ASCC) is a powerful method for coupling aryl and alkyl alcohols with SuFEx-compatible functional groups. With its hallmark favorable kinetics and exceptional product yields, ASCC streamlines the synthetic workflow, simplifies the purification process, and is ideally suited for discovering functional molecules. We showcase the versatility and practicality of the ASCC reaction as a tool for the late-stage derivatization of bioactive molecules and in the array synthesis of sulfonate-linked, high-potency, microtubule targeting agents (MTAs) that exhibit nanomolar anticancer activity against multidrug-resistant cancer cell lines. These findings underscore ASCC's promise as a robust platform for drug discovery.
PubMed: 38487227
DOI: 10.1039/d3sc05729a
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.57 Å)
Structure validation

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