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SummaryStructural detailsExperimental detailsFunctional detailsSequence NeighborHistoryDownloads

22VT

Structure of human MCM2-7 single hexamer with MCM3-WHD attached to MCM2-CTD, containing Meier-Gorlin Syndrome mutation (MCM3-Q761L)

Chains
EntityAsym IDsNumber of Exact matches
1A46
2B
3C20
4D35
5E35
6F29
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256158

PDB entries from 2026-07-08

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