作者
Hirokazu Satoh, Yoshimi Nakano, Hideki Shibata, Masatoshi Maki
发表日期
2002/11/4
期刊
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics
卷号
1600
期号
1-2
页码范围
61-67
出版商
Elsevier
简介
The apoptosis-linked protein ALG-2 is a Ca2+-binding protein that belongs to the penta-EF-hand (PEF) protein family. ALG-2 forms a homodimer, a heterodimer with another PEF protein, peflin, and a complex with its interacting protein, named Alix or AIP1. We previously identified annexin XI as a novel ALG-2-binding partner. Both the N-terminal regulatory domain of annexin XI (Anx11N) and the ALG-2-binding domain of Alix/AIP1 are rich in Pro, Gly, Ala, Tyr and Gln. This PGAYQ-biased amino acid composition is also found in the N-terminal extension of annexin VII (Anx7N). Using recombinant ALG-2 proteins and the glutathione S-transferase (GST) fusion proteins of Anx7N and Anx11N, the direct Ca2+-dependent interaction was analyzed by a biotin-tagged ALG-2 overlay assay and by a real-time interaction analysis with a surface plasmon resonance (SPR) biosensor. Both GST–Anx7N and GST–Anx11N …
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