Structural proteomics defines a sequential priming mechanism for the progesterone receptor

Structural proteomics defines a sequential priming mechanism for the progesterone receptor

Abstract The progesterone receptor (PR) is a steroid-responsive nuclear receptor with two isoforms: PR-A and PR-B. Disruption of PR-A:PR-B signaling is associated with breast cancer through interactions with oncogenic co-regulatory proteins (CoRs). However, molecular details of isoform-specific PR-C...

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Main Authors: Matthew D. Mann, Min Wang, Josephine C. Ferreon, Phoebe S. Tsoi, Michael P. Suess, Antrix Jain, Anna Malovannaya, Roberto Vera Alvarez, Bruce D. Pascal, Raj Kumar, Dean P. Edwards, Patrick R. Griffin
Format: Article
Language:English
Published: Nature Portfolio 2025-05-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-59458-y
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https://doi.org/10.1038/s41467-025-59458-y

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