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6CIL

PRE-REACTION COMPLEX, RAG1(E962Q)/2-INTACT/INTACT 12/23RSS COMPLEX IN MN2+

Summary for 6CIL
Entry DOI10.2210/pdb6cil/pdb
Related4WWX 5ZDZ 5ZE0 5ZE1 5ZE2 6CG0 6CIJ 6CIK 6CIM
DescriptorV(D)J recombination-activating protein 1, V(D)J recombination-activating protein 2, High mobility group protein B1, ... (9 entities in total)
Functional Keywordsvdj recombination, rss, rag1/2, recombination, recombination-dna complex, recombination/dna
Biological sourceMus musculus (Mouse)
More
Total number of polymer chains9
Total formula weight301161.41
Authors
Chuenchor, W.,Chen, X.,Kim, M.S.,Gellert, M.,Yang, W. (deposition date: 2018-02-24, release date: 2018-04-25, Last modification date: 2023-10-04)
Primary citationKim, M.S.,Chuenchor, W.,Chen, X.,Cui, Y.,Zhang, X.,Zhou, Z.H.,Gellert, M.,Yang, W.
Cracking the DNA Code for V(D)J Recombination.
Mol. Cell, 70:358-370.e4, 2018
Cited by
PubMed Abstract: To initiate V(D)J recombination for generating the adaptive immune response of vertebrates, RAG1/2 recombinase cleaves DNA at a pair of recombination signal sequences, the 12- and 23-RSS. We have determined crystal and cryo-EM structures of RAG1/2 with DNA in the pre-reaction and hairpin-forming complexes up to 2.75 Å resolution. Both protein and DNA exhibit structural plasticity and undergo dramatic conformational changes. Coding-flank DNAs extensively rotate, shift, and deform for nicking and hairpin formation. Two intertwined RAG1 subunits crisscross four times between the asymmetric pair of severely bent 12/23-RSS DNAs. Location-sensitive bending of 60° and 150° in 12- and 23-RSS spacers, respectively, must occur for RAG1/2 to capture the nonamers and pair the heptamers for symmetric double-strand breakage. DNA pairing is thus sequence-context dependent and structure specific, which partly explains the "beyond 12/23" restriction. Finally, catalysis in crystallo reveals the process of DNA hairpin formation and its stabilization by interleaved base stacking.
PubMed: 29628308
DOI: 10.1016/j.molcel.2018.03.008
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (4.15 Å)
Structure validation

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