Molecular basis for nuclear accumulation and targeting of the inhibitor of apoptosis BIRC2-Reference-Cited by-同舟云学术

Molecular basis for nuclear accumulation and targeting of the inhibitor of apoptosis BIRC2

Published:2023-07-31 Issue:9 Volume:30 Page:1265-1274
ISSN:1545-9993
Container-title:Nature Structural & Molecular Biology
language:en
Short-container-title:Nat Struct Mol Biol

Author:

Tencer Adam H.,Yu Yucong,Causse Sebastien Z.,Campbell Grant R.^ORCID,Klein Brianna J.^ORCID,Xuan Hongwen,Cartier Jessy,Miles Mark A.^ORCID,Gaurav Nitika,Zadoroznyj Aymeric,Holt Tina A.^ORCID,Wen Hong^ORCID,Hawkins Christine J.^ORCID,Spector Stephen A.^ORCID,Dubrez Laurence^ORCID,Shi Xiaobing^ORCID,Kutateladze Tatiana G.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Molecular Biology,Structural Biology

Link

https://www.nature.com/articles/s41594-023-01044-1.pdf

Reference53 articles.

1. Gyrd-Hansen, M. & Meier, P. IAPs: from caspase inhibitors to modulators of NF-kappaB, inflammation and cancer. Nat. Rev. Cancer 10, 561–574 (2010).

2. Estornes, Y. & Bertrand, M. J. IAPs, regulators of innate immunity and inflammation. Semin. Cell Dev. Biol. 39, 106–114 (2015).

3. Mehrotra, S. et al. IAP regulation of metastasis. Cancer Cell 17, 53–64 (2010).

4. Swingler, S., Mann, A. M., Zhou, J., Swingler, C. & Stevenson, M. Apoptotic killing of HIV-1-infected macrophages is subverted by the viral envelope glycoprotein. PLoS Pathog. 3, 1281–1290 (2007).

5. Wang, X., Ragupathy, V., Zhao, J. & Hewlett, I. Molecules from apoptotic pathways modulate HIV-1 replication in Jurkat cells. Biochem. Biophys. Res. Commun. 414, 20–24 (2011).

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