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Jonathan M Elkins

Showing results (51-60 of 78) with videos related to

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Journal of Medicinal Chemistry|August 31, 2021
Discovery of a Potent Dual SLK/STK10 Inhibitor Based on a Maleimide ScaffoldRicardo A M Serafim, Fiona J Sorrell, Benedict-Tilman Berger, et al.
Journal of Medicinal Chemistry|October 7, 2022
Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular ActivityRoss Collins, Hyunah Lee, D Heulyn Jones, et al.
Communications Biology|July 24, 2024
A ligand discovery toolbox for the WWE domain family of human E3 ligasesLena Münzker, Serah W Kimani, Milan M Fowkes, et al.
Nature Communications|May 11, 2026
Structural insights into cobalamin loading and reactivation of human methionine synthaseDouglas S M Ferreira, Katie McLennan, Calum Diamond, et al.
Journal of Medicinal Chemistry|August 3, 2021
Discovery and Characterization of Selective and Ligand-Efficient DYRK InhibitorsScott H Henderson, Fiona Sorrell, James Bennett, et al.
Cell Chemical Biology|January 26, 2021
Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2Benedict-Tilman Berger, Marta Amaral, Daria B Kokh, et al.
Nucleic Acids Research|June 16, 2023
Updated protein domain annotation of the PARP protein family sheds new light on biological functionMarcin J Suskiewicz, Deeksha Munnur, Øyvind Strømland, et al.
European Journal of Medicinal Chemistry|November 19, 2013
Structural determinants for ERK5 (MAPK7) and leucine rich repeat kinase 2 activities of benzo[e]pyrimido-[5,4-b]diazepine-6(11H)-onesXianming Deng, Jonathan M Elkins, Jinwei Zhang, et al.
Journal of Medicinal Chemistry|September 25, 2012
Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine BTania Tahtouh, Jonathan M Elkins, Panagis Filippakopoulos, et al.
The Journal of Biological Chemistry|June 4, 2002
Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural familyKirsty S Hewitson, Luke A McNeill, Madeline V Riordan, et al.
Pageof 8

Showing results (51-60 of 78) with videos related to

Sort By:
Pageof 8
Journal of Medicinal Chemistry|August 31, 2021
Discovery of a Potent Dual SLK/STK10 Inhibitor Based on a Maleimide ScaffoldRicardo A M Serafim, Fiona J Sorrell, Benedict-Tilman Berger, et al.
Journal of Medicinal Chemistry|October 7, 2022
Comparative Analysis of Small-Molecule LIMK1/2 Inhibitors: Chemical Synthesis, Biochemistry, and Cellular ActivityRoss Collins, Hyunah Lee, D Heulyn Jones, et al.
Communications Biology|July 24, 2024
A ligand discovery toolbox for the WWE domain family of human E3 ligasesLena Münzker, Serah W Kimani, Milan M Fowkes, et al.
Nature Communications|May 11, 2026
Structural insights into cobalamin loading and reactivation of human methionine synthaseDouglas S M Ferreira, Katie McLennan, Calum Diamond, et al.
Journal of Medicinal Chemistry|August 3, 2021
Discovery and Characterization of Selective and Ligand-Efficient DYRK InhibitorsScott H Henderson, Fiona Sorrell, James Bennett, et al.
Cell Chemical Biology|January 26, 2021
Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2Benedict-Tilman Berger, Marta Amaral, Daria B Kokh, et al.
Nucleic Acids Research|June 16, 2023
Updated protein domain annotation of the PARP protein family sheds new light on biological functionMarcin J Suskiewicz, Deeksha Munnur, Øyvind Strømland, et al.
European Journal of Medicinal Chemistry|November 19, 2013
Structural determinants for ERK5 (MAPK7) and leucine rich repeat kinase 2 activities of benzo[e]pyrimido-[5,4-b]diazepine-6(11H)-onesXianming Deng, Jonathan M Elkins, Jinwei Zhang, et al.
Journal of Medicinal Chemistry|September 25, 2012
Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine BTania Tahtouh, Jonathan M Elkins, Panagis Filippakopoulos, et al.
The Journal of Biological Chemistry|June 4, 2002
Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural familyKirsty S Hewitson, Luke A McNeill, Madeline V Riordan, et al.
Pageof 8