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7KZT

Structure of the human fanconi anaemia Core-UBE2T-ID-DNA complex in intermediate state

This is a non-PDB format compatible entry.
Summary for 7KZT
Entry DOI10.2210/pdb7kzt/pdb
EMDB information23089
DescriptorFanconi anemia group A protein, Ubiquitin-conjugating enzyme E2 T, Fanconi anemia, complementation group I, ... (15 entities in total)
Functional Keywordscomplex, ligase, ligase-dna complex, ligase/dna
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains19
Total formula weight1506427.30
Authors
Wang, S.L.,Pavletich, N.P. (deposition date: 2020-12-10, release date: 2021-03-10, Last modification date: 2024-10-23)
Primary citationWang, S.,Wang, R.,Peralta, C.,Yaseen, A.,Pavletich, N.P.
Structure of the FA core ubiquitin ligase closing the ID clamp on DNA.
Nat.Struct.Mol.Biol., 28:300-309, 2021
Cited by
PubMed Abstract: The Fanconi anemia (FA) pathway is essential for the repair of DNA interstrand crosslinks. Central to the pathway is the FA core complex, a ubiquitin ligase of nine subunits that monoubiquitinates the FANCI-FANCD2 (ID) DNA clamp. The 3.1 Å structure of the 1.1-MDa human FA core complex, described here, reveals an asymmetric assembly with two copies of all but the FANCC, FANCE and FANCF subunits. The asymmetry is crucial, as it prevents the binding of a second FANCC-FANCE-FANCF subcomplex that inhibits the recruitment of the UBE2T ubiquitin conjugating enzyme, and instead creates an ID binding site. A single active site then ubiquitinates FANCD2 and FANCI sequentially. We also present the 4.2-Å structures of the human core-UBE2T-ID-DNA complex in three conformations captured during monoubiquitination. They reveal the core-UBE2T complex remodeling the ID-DNA complex, closing the clamp on the DNA before ubiquitination. Monoubiquitination then prevents clamp opening after release from the core.
PubMed: 33686268
DOI: 10.1038/s41594-021-00568-8
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.2 Å)
Structure validation

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