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5STM

PanDDA analysis group deposition -- Aar2/RNaseH in complex with fragment P03A03 from the F2X-Universal Library

Summary for 5STM
Entry DOI10.2210/pdb5stm/pdb
Group depositionPanDDA analysis group deposition (G_1002241)
DescriptorPre-mRNA-splicing factor 8, A1 cistron-splicing factor AAR2, 5-bromo-2-hydrazinylpyridine, ... (4 entities in total)
Functional Keywordsfragmax, fragmaxapp, fragment screening, rnaseh like domain, u5 snrnp assembly, splicing
Biological sourceSaccharomyces cerevisiae S288C
More
Total number of polymer chains2
Total formula weight66087.00
Authors
Barthel, T.,Wollenhaupt, J.,Lima, G.M.A.,Wahl, M.C.,Weiss, M.S. (deposition date: 2022-08-26, release date: 2022-11-02, Last modification date: 2024-05-22)
Primary citationBarthel, T.,Wollenhaupt, J.,Lima, G.M.A.,Wahl, M.C.,Weiss, M.S.
Large-Scale Crystallographic Fragment Screening Expedites Compound Optimization and Identifies Putative Protein-Protein Interaction Sites.
J.Med.Chem., 65:14630-14641, 2022
Cited by
PubMed Abstract: The identification of starting points for compound development is one of the key steps in early-stage drug discovery. Information-rich techniques such as crystallographic fragment screening can potentially increase the efficiency of this step by providing the structural information of the binding mode of the ligands in addition to the mere binding information. Here, we present the crystallographic screening of our 1000-plus-compound F2X-Universal Library against the complex of the yeast spliceosomal Prp8 RNaseH-like domain and the snRNP assembly factor Aar2. The observed 269 hits are distributed over 10 distinct binding sites on the surface of the protein-protein complex. Our work shows that hit clusters from large-scale crystallographic fragment screening campaigns identify known interaction sites with other proteins and suggest putative additional interaction sites. Furthermore, the inherent binding pose validation within the hit clusters may accelerate downstream compound optimization.
PubMed: 36260741
DOI: 10.1021/acs.jmedchem.2c01165
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.65 Å)
Structure validation

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