4B3B

Humanised monomeric RadA in complex with FHTA tetrapeptide

Summary for 4B3B

• Entry DOI: 10.2210/pdb4b3b/pdb
• Related: 1PZN 4A6P 4A6X 4A74 4A7O 4B2I 4B2L 4B2P 4B32 4B33 4B34 4B35 4B3C 4B3D
• Descriptor: DNA REPAIR AND RECOMBINATION PROTEIN RADA, FHTA TETRAPEPTIDE, PHOSPHATE ION, ... (4 entities in total)
• Functional Keywords: hydrolase-peptide complex, recombinase, thermostable, humanised, peptide-binding, hydrolase/peptide
• Biological source: PYROCOCCUS FURIOSUS; More
• Total number of polymer chains: 2
• Total formula weight: 26096.68

Authors

Scott, D.E.,Ehebauer, M.T.,Pukala, T.,Marsh, M.,Blundell, T.L.,Venkitaraman, A.R.,Abell, C.,Hyvonen, M. (deposition date: 2012-07-23, release date: 2013-02-27, Last modification date: 2024-10-16)

Primary citation

Scott, D.E.,Ehebauer, M.T.,Pukala, T.,Marsh, M.,Blundell, T.L.,Venkitaraman, A.R.,Abell, C.,Hyvonen, M.
Using a Fragment-Based Approach to Target Protein-Protein Interactions.
Chembiochem, 14:332-, 2013

PubMed Abstract: The ability to identify inhibitors of protein-protein interactions represents a major challenge in modern drug discovery and in the development of tools for chemical biology. In recent years, fragment-based approaches have emerged as a new methodology in drug discovery; however, few examples of small molecules that are active against chemotherapeutic targets have been published. Herein, we describe the fragment-based approach of targeting the interaction between the tumour suppressor BRCA2 and the recombination enzyme RAD51; it makes use of a screening pipeline of biophysical techniques that we expect to be more generally applicable to similar targets. Disruption of this interaction in vivo is hypothesised to give rise to cellular hypersensitivity to radiation and genotoxic drugs. We have used protein engineering to create a monomeric form of RAD51 by humanising a thermostable archaeal orthologue, RadA, and used this protein for fragment screening. The initial fragment hits were thoroughly validated biophysically by isothermal titration calorimetry (ITC) and NMR techniques and observed by X-ray crystallography to bind in a shallow surface pocket that is occupied in the native complex by the side chain of a phenylalanine from the conserved FxxA interaction motif found in BRCA2. This represents the first report of fragments or any small molecule binding at this protein-protein interaction site.

PubMed: 23344974
DOI: 10.1002/CBIC.201200521

Experimental method

X-RAY DIFFRACTION (1.193 Å)