Decoding P4-ATPase substrate interactions
Author:
Affiliation:
1. Department of Biological Sciences, Vanderbilt University, 1161 21st Ave South, Nashville, TN, USA
Funder
National Institute of General Medical Sciences
Publisher
Informa UK Limited
Subject
Molecular Biology,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10409238.2016.1237934
Reference102 articles.
1. Loss of P4 ATPases Drs2p and Dnf3p Disrupts Aminophospholipid Transport and Asymmetry in Yeast Post-Golgi Secretory Vesicles
2. Viral apoptotic mimicry
3. P4-ATPases as Phospholipid Flippases—Structure, Function, and Enigmas
4. ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia
5. Evolution of Substrate Specificities in the P-Type ATPase Superfamily
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