Showing results (11-20 of 37) with videos related to
Sort By:
Pageof 4
European Biophysics Journal : EBJ|May 26, 2006
Optimizing crystal volume for neutron diffraction: D-xylose isomeraseEdward H Snell, Mark J van der Woerd, Michael Damon, et al.Acta Crystallographica. Section D, Biological Crystallography|February 18, 2014
Neutron structure of the cyclic glucose-bound xylose isomerase E186Q mutantParthapratim Munshi, Edward H Snell, Mark J van der Woerd, et al.Biochemistry|May 17, 2014
Water channel in the binding site of a high affinity anti-methotrexate antibodySusan Gayda, Kenton L Longenecker, Sharmila Manoj, et al.Bioorganic & Medicinal Chemistry Letters|April 26, 2018
Targeting lysine specific demethylase 4A (KDM4A) tandem TUDOR domain - A fragment based approachAnup K Upadhyay, Russell A Judge, Leiming Li, et al.Bioorganic & Medicinal Chemistry Letters|March 26, 2016
Creation of a S1P Lyase bacterial surrogate for structure-based drug designMaria A Argiriadi, David Banach, Elzbieta Radziejewska, et al.Communications Chemistry|October 29, 2023
Cryo-EM structure of human PAPP-A2 and mechanism of substrate recognitionJanani Sridar, Amirhossein Mafi, Russell A Judge, et al.ACS Medicinal Chemistry Letters|December 21, 2016
Turning a Substrate Peptide into a Potent Inhibitor for the Histone Methyltransferase SETD8Russell A Judge, Haizhong Zhu, Anup K Upadhyay, et al.Journal of Biomolecular Screening|September 8, 2006
Kinase drug discovery by affinity selection/mass spectrometry (ASMS): application to DNA damage checkpoint kinase Chk1Kenneth M Comess, Jonathan D Trumbull, Chang Park, et al.Bioorganic & Medicinal Chemistry Letters|November 26, 2010
N-aryl-benzimidazolones as novel small molecule HSP90 inhibitorsMilan Bruncko, Stephen K Tahir, Xiaohong Song, et al.Bioorganic & Medicinal Chemistry|February 9, 2007
Discovery of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of potent and selective checkpoint kinase 1 inhibitorsYunsong Tong, Akiyo Claiborne, Kent D Stewart, et al.Pageof 4