A Disease-Causing Variant in PCNA Disrupts a Promiscuous Protein Binding Site
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文摘

Disease mutation causes large deformation of the binding pocket in PCNA.

Disrupts binding of some, but not all, interaction partners.

Binding site structure is pliable and accommodates ligands idiosyncratically.

Loss of interaction with RNase H2B suggests an RER defect in patients.

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