PDBsum entry 5v5e

Viral protein / inhibitor

PDB id: 5v5e

Contents

Protein chains

188 a.a.

Ligands

8N4 ×3

Waters ×43

References listed in PDB file

Key reference

• Title: Allosteric inhibitors, Crystallography, And comparative analysis reveal network of coordinated movement across human herpesvirus proteases.
• Authors: T.M.Acker, J.E.Gable, M.F.Bohn, P.Jaishankar, M.C.Thompson, J.S.Fraser, A.R.Renslo, C.S.Craik.
• Ref.: J Am Chem Soc, 2017, 139, 11650-11653. [DOI no: 10.1021/jacs.7b04030]
• PubMed id: 28759216

Abstract

Targeting of cryptic binding sites represents an attractive but underexplored approach to modulating protein function with small molecules. Using the dimeric protease (Pr) from Kaposi's sarcoma-associated herpesvirus (KSHV) as a model system, we sought to dissect a putative allosteric network linking a cryptic site at the dimerization interface to enzyme function. Five cryogenic X-ray structures were solved of the monomeric protease with allosteric inhibitors bound to the dimer interface site. Distinct coordinated movements captured by the allosteric inhibitors were also revealed as alternative states in room-temperature X-ray data and comparative analyses of other dimeric herpesvirus proteases. A two-step mechanism was elucidated through detailed kinetic analyses and suggests an enzyme isomerization model of inhibition. Finally, a representative allosteric inhibitor from this class was shown to be efficacious in a cellular model of viral infectivity. These studies reveal a coordinated dynamic network of atomic communication linking cryptic binding site occupancy and allosteric inactivation of KHSV Pr that can be exploited to target other members of this clinically relevant family of enzymes.