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6AKO

Crystal Structure of FOXC2 DBD Bound to DBE2 DNA

Summary for 6AKO
Entry DOI10.2210/pdb6ako/pdb
DescriptorDNA (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 Keywordsfoxc; dna binding domain; dna recognition; crystal structure; lymphoedema distichiasis syndrome, dna binding protein-dna complex, dna binding protein/dna
Biological sourceHomo sapiens
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Total number of polymer chains3
Total formula weight22146.90
Authors
Chen, X.,Wei, H.,Li, J.,Liang, X.,Dai, S.,Jiang, L.,Guo, M.,Chen, Y. (deposition date: 2018-09-03, release date: 2019-02-06, Last modification date: 2023-11-22)
Primary citationChen, 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: 30722065
DOI: 10.1093/nar/gkz077
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.396 Å)
Structure validation

226707

数据于2024-10-30公开中

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