6AKO
Crystal Structure of FOXC2 DBD Bound to DBE2 DNA
Summary for 6AKO
Entry DOI | 10.2210/pdb6ako/pdb |
Descriptor | DNA (5'-D(CP*AP*AP*AP*AP*TP*GP*TP*AP*AP*AP*CP*AP*AP*GP*A)-3'), DNA (5'-D(TP*CP*TP*TP*GP*TP*TP*TP*AP*CP*AP*TP*TP*TP*TP*G)-3'), Forkhead box protein C2, ... (5 entities in total) |
Functional Keywords | foxc; dna binding domain; dna recognition; crystal structure; lymphoedema distichiasis syndrome, dna binding protein-dna complex, dna binding protein/dna |
Biological source | Homo sapiens More |
Total number of polymer chains | 3 |
Total formula weight | 22146.90 |
Authors | |
Primary citation | Chen, X.,Wei, H.,Li, J.,Liang, X.,Dai, S.,Jiang, L.,Guo, M.,Qu, L.,Chen, Z.,Chen, L.,Chen, Y. Structural basis for DNA recognition by FOXC2. Nucleic Acids Res., 47:3752-3764, 2019 Cited by PubMed Abstract: The FOXC family of transcription factors (FOXC1 and FOXC2) plays essential roles in the regulation of embryonic, ocular, and cardiac development. Mutations and abnormal expression of FOXC proteins are implicated in genetic diseases as well as cancer. In this study, we determined two crystal structures of the DNA-binding domain (DBD) of human FOXC2 protein, in complex with different DNA sites. The FOXC2-DBD adopts the winged-helix fold with helix H3 contributing to all the base specific contacts, while the N-terminus, wing 1, and the C-terminus of FOXC2-DBD all make additional contacts with the phosphate groups of DNA. Our structural, biochemical, and bioinformatics analyses allow us to revise the previously proposed DNA recognition mechanism and provide a model of DNA binding for the FOXC proteins. In addition, our structural analysis and accompanying biochemical assays provide a molecular basis for understanding disease-causing mutations in FOXC1 and FOXC2. PubMed: 30722065DOI: 10.1093/nar/gkz077 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.396 Å) |
Structure validation
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