A gold revision of the Golgi Dynamics (GOLD) domain structure and associated cell functionalities

FEBS Letters

article

Luis Felipe S. Mendes¹  Antonio J. Costa-Filho¹ 

[1] Laboratório de Biofísica Molecular, Departamento de Física, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo

关键词: ACBD3;    FYCO1;    GOLD domain;    protein-protein interaction;    SEC14-like proteins;    secretory pathway;    TMED/p24 proteins;    TRAM adaptor with GOLD domain;    β-sandwich-like fold;   

DOI  :  10.1002/1873-3468.14300

来源: John Wiley & Sons Ltd.

【 摘 要 】

The classical secretory pathway is the key membrane-based delivery system in eukaryotic cells. Several families of proteins involved in the secretory pathway, with functionalities going from cargo sorting receptors to the maintenance and dynamics of secretory organelles, share soluble globular domains predicted to mediate protein–protein interactions. One of them is the ‘Golgi Dynamics’ (GOLD) domain, named after its strong association with the Golgi apparatus. There are many GOLD-containing protein families, such as the transmembrane emp24 domain-containing proteins (TMED/p24 family), animal SEC14-like proteins, human Golgi resident protein ACBD3, a splice variant of TICAM2 called TRAM with GOLD domain, and FYCO1. Here, we critically review the state-of-the-art knowledge of the structures and functions of the main representatives of GOLD-containing proteins in vertebrates. We provide the first unified description of the GOLD domain structure across different families since the first high-resolution structure was determined. With a brand-new update on the definition of the GOLD domain, we also discuss how its tertiary structure fits the β-sandwich-like fold map and give exciting new directions for forthcoming studies.

【 授权许可】

Unknown