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9FOI

Structure of human KCTD1

9FOI の概要
エントリーDOI10.2210/pdb9foi/pdb
分子名称BTB/POZ domain-containing protein KCTD1, IODIDE ION, SODIUM ION, ... (6 entities in total)
機能のキーワードkctd1, potassium channel tetramerization domain containing 1, btb, ligase
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数5
化学式量合計148610.61
構造登録者
主引用文献Pinkas, D.M.,Bufton, J.C.,Hunt, A.E.,Manning, C.E.,Richardson, W.,Bullock, A.N.
A BTB extension and ion-binding domain contribute to the pentameric structure and TFAP2A binding of KCTD1.
Structure, 32:1586-1593.e4, 2024
Cited by
PubMed Abstract: KCTD family proteins typically assemble into cullin-RING E3 ligases. KCTD1 is an atypical member that functions instead as a transcriptional repressor. Mutations in KCTD1 cause developmental abnormalities and kidney fibrosis in scalp-ear-nipple syndrome. Here, we present unexpected mechanistic insights from the structure of human KCTD1. Disease-causing mutation P20S maps to an unrecognized extension of the BTB domain that contributes to both its pentameric structure and TFAP2A binding. The C-terminal domain (CTD) shares its fold and pentameric assembly with the GTP cyclohydrolase I feedback regulatory protein (GFRP) despite lacking discernible sequence similarity. Most surprisingly, the KCTD1 CTD establishes a central channel occupied by alternating sodium and iodide ions that restrict TFAP2A dissociation. The elucidation of the structure redefines the KCTD1 BTB domain fold and identifies an unexpected ion-binding site for future study of KCTD1's function in the ectoderm, neural crest, and kidney.
PubMed: 39191250
DOI: 10.1016/j.str.2024.07.023
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.71 Å)
構造検証レポート
Validation report summary of 9foi
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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