7JXV

ANTH domain of CALM (clathrin-assembly lymphoid myeloid leukemia protein) bound to ubiquitin

7JXV の概要

• エントリーDOI: 10.2210/pdb7jxv/pdb
• 分子名称: Phosphatidylinositol-binding clathrin assembly protein, Ubiquitin (3 entities in total)
• 機能のキーワード: complex, endocytosis
• 由来する生物種: Rattus norvegicus (Rat); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 41898.00

構造登録者

Pashkova, N.,Gakhar, L.,Schnicker, N.J.,Piper, R.C. (登録日: 2020-08-28, 公開日: 2021-08-04, 最終更新日: 2023-10-18)

主引用文献

Pashkova, N.,Gakhar, L.,Yu, L.,Schnicker, N.J.,Minard, A.Y.,Winistorfer, S.,Johnson, I.E.,Piper, R.C.
ANTH domains within CALM, HIP1R, and Sla2 recognize ubiquitin internalization signals.
Elife, 10:-, 2021

PubMed Abstract: Attachment of ubiquitin (Ub) to cell surface proteins serves as a signal for internalization via clathrin-mediated endocytosis (CME). How ubiquitinated membrane proteins engage the internalization apparatus remains unclear. The internalization apparatus contains proteins such as Epsin and Eps15, which bind Ub, potentially acting as adaptors for Ub-based internalization signals. Here, we show that additional components of the endocytic machinery including CALM, HIP1R, and Sla2 bind Ub via their N-terminal ANTH domain, a domain belonging to the superfamily of ENTH and VHS domains. Structural studies revealed that Ub binds with µM affinity to a unique C-terminal region within the ANTH domain not found in ENTH domains. Functional studies showed that combined loss of Ub-binding by ANTH-domain proteins and other Ub-binding domains within the yeast internalization apparatus caused defects in the Ub-dependent internalization of the GPCR Ste2 that was engineered to rely exclusively on Ub as an internalization signal. In contrast, these mutations had no effect on the internalization of Ste2 engineered to use an alternate Ub-independent internalization signal. These studies define new components of the internalization machinery that work collectively with Epsin and Eps15 to specify recognition of Ub as an internalization signal.

PubMed: 34821552
DOI: 10.7554/eLife.72583

実験手法

X-RAY DIFFRACTION (2.35 Å)