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8BWD

Crystal structure of human Twisted gastrulation protein homolog 1 (TWSG1), crystal form 1

8BWD の概要
エントリーDOI10.2210/pdb8bwd/pdb
分子名称Twisted gastrulation protein homolog 1, SULFATE ION (3 entities in total)
機能のキーワードtwisted gastrulation protein homolog 1 (twsg1), transforming growth factor beta (tgf-beta) signalling pathway, extracellular protein, disulfide rich domains., signaling protein
由来する生物種Homo sapiens (human)
タンパク質・核酸の鎖数2
化学式量合計47235.58
構造登録者
主引用文献Malinauskas, T.,Moore, G.,Rudolf, A.F.,Eggington, H.,Belnoue-Davis, H.L.,El Omari, K.,Griffiths, S.C.,Woolley, R.E.,Duman, R.,Wagner, A.,Leedham, S.J.,Baldock, C.,Ashe, H.L.,Siebold, C.
Molecular mechanism of BMP signal control by Twisted gastrulation.
Nat Commun, 15:4976-4976, 2024
Cited by
PubMed Abstract: Twisted gastrulation (TWSG1) is an evolutionarily conserved secreted glycoprotein which controls signaling by Bone Morphogenetic Proteins (BMPs). TWSG1 binds BMPs and their antagonist Chordin to control BMP signaling during embryonic development, kidney regeneration and cancer. We report crystal structures of TWSG1 alone and in complex with a BMP ligand, Growth Differentiation Factor 5. TWSG1 is composed of two distinct, disulfide-rich domains. The TWSG1 N-terminal domain occupies the BMP type 1 receptor binding site on BMPs, whereas the C-terminal domain binds to a Chordin family member. We show that TWSG1 inhibits BMP function in cellular signaling assays and mouse colon organoids. This inhibitory function is abolished in a TWSG1 mutant that cannot bind BMPs. The same mutation in the Drosophila TWSG1 ortholog Tsg fails to mediate BMP gradient formation required for dorsal-ventral axis patterning of the early embryo. Our studies reveal the evolutionarily conserved mechanism of BMP signaling inhibition by TWSG1.
PubMed: 38862520
DOI: 10.1038/s41467-024-49065-8
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.63 Å)
構造検証レポート
Validation report summary of 8bwd
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2026-02-11に公開中

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