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Journal of Medicinal Chemistry|November 11, 2005
Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferaseQian Wu, Christine L Gee, Frank Lin, et al.
Nature Communications|March 25, 2026
Substrate-interacting pore loops of two ATPase subunits determine the degradation efficiency of the 26S proteasomeErika López-Alfonzo, Ayush Saurabh, Sahar Zarafshan, et al.
Journal of Medicinal Chemistry|September 12, 2007
Enzyme adaptation to inhibitor binding: a cryptic binding site in phenylethanolamine N-methyltransferaseChristine L Gee, Nyssa Drinkwater, Joel D A Tyndall, et al.
Structure (London, England : 1993)|April 18, 2007
Structural basis for selective inhibition of Mycobacterium tuberculosis protein tyrosine phosphatase PtpBChristoph Grundner, Dominique Perrin, Rob Hooft van Huijsduijnen, et al.
Nature Structural & Molecular Biology|April 11, 2025
NUB1 traps unfolded FAT10 for ubiquitin-independent degradation by the 26S proteasomeConnor Arkinson, Ken C Dong, Christine L Gee, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|June 8, 2007
Crystallization and preliminary X-ray diffraction of the Munc18c-syntaxin4 (1-29) complexCatherine F Latham, Shu Hong Hu, Christine L Gee, et al.
Biochimica Et Biophysica Acta|May 17, 2005
Disulfide-linked dimers of human adrenaline synthesizing enzyme PNMT are catalytically activeChristine L Gee, Amanda Nourse, A-Yen Hsin, et al.
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