6S4L

Structure of human KCTD1

6S4L の概要

• エントリーDOI: 10.2210/pdb6s4l/pdb
• 分子名称: BTB/POZ domain-containing protein KCTD1, SODIUM ION, IODIDE ION, ... (4 entities in total)
• 機能のキーワード: kctd1, signaling protein
• 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: 134157.36

構造登録者

Pinkas, D.M.,Bufton, J.C.,Fox, A.E.,Pike, A.C.W.,Newman, J.A.,Krojer, T.,Shrestha, L.,Burgess-Brown, N.A.,von Delft, F.,Arrowsmith, C.,Edwards, A.,Bountra, C.,Bullock, A.N. (登録日: 2019-06-28, 公開日: 2020-07-15, 最終更新日: 2025-06-25)

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

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

実験手法

X-RAY DIFFRACTION (2.42 Å)