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44NI

Crystal structure of a reduced form of mouse MsrA

This is a non-PDB format compatible entry.
Summary for 44NI
Entry DOI10.2210/pdb44ni/pdb
DescriptorMitochondrial peptide methionine sulfoxide reductase (1 entity in total)
Functional Keywordsreduced form, oxidoreductase
Biological sourceMus musculus (house mouse)
Total number of polymer chains1
Total formula weight26023.40
Authors
Primary citationShin, B.,Hawkes, H.K.,Park, S.,Ki, H.,Kim, S.,Shah, F.,Di Trapani, G.,Tonissen, K.F.,Hwang, K.Y.
Structural basis for cysteine-linked redox-state plasticity in mammalian methionine sulfoxide reductase A.
Redox Biol, 97:104436-104436, 2026
Cited by
PubMed Abstract: Methionine sulfoxide reductase A (MsrA) protects proteins from oxidative damage through cysteine-based redox cycling, but how mammalian MsrA is structurally regulated during oxidation and reductive recycling has remained unclear. We report three crystal structures of mouse MsrA (mMsrA) that capture distinct redox states - reduced (3.0 Å), BME-trapped intermediate-like (BTIL; 1.6 Å), and oxidized (1.9 Å) - and reveal an unrecognized layer of regulation centered on Cys107. The BTIL structure visualizes catalytic Cys72 as a mixed disulfide with β-mercaptoethanol (BME) alongside a sulfenic acid at Cys107, a configuration not previously observed. The oxidized structure resolves the canonical Cys72-Cys218 disulfide together with an unexpected Cys107-Cys227 pairing that locks a C-terminal loop into a cap over the active site. LC-MS/MS mapping, MD simulations, activity assays, and thioredoxin (Trx)-trapping experiments converge on a model in which Cys72 drives catalysis, while Cys107-mediated disulfide rearrangement and Cys227-directed Trx entry gate substrate access and enzymatic regeneration - defining a noncanonical oxidized state that expands the mechanistic repertoire of mammalian MsrA under oxidative stress.
PubMed: 42860110
DOI: 10.1016/j.redox.2026.104436
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3 Å)
Structure validation

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PDB entries from 2026-10-28

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