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Results and discussion Primary fragment screening by X-ray crystallography Due to its broad affinity detection range (nanomolar to millimolar) and unique ability to initiate rational drug design 30 , we carried out a crystallographic fragment screen against TRF1 TRFH at the XChem facility of the Diamond Light Source 30

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Therefore, this in silico mutational analysis reinforces the key role of the transient residue Gly 376 for maintaining the GTP-induced inhibition dynamics