Protein Structures

The following table showcases the protein structures discovered and characterized by the CQMED team in collaboration with our partners. These structures have provided valuable insights into kinase biology and have the potential to inform the development of new therapeutic strategies.

YearPDB CodeDescription
20248V42Structure of Human Vaccinia-related Kinase 1 (VRK1) Bound to ACH000400
20227S6ULeishmania infantum Glycogen Synthase Kinase 3 beta bound to AZD5438
20227S6VLeishmania infantum Glycogen Synthase Kinase 3 beta bound to CGP60474
20227LQDStructure of Human MPS1 (TTK) covalently bound to RMS-07 inhibitor
20217NAACrystal structure of Mycobacterium tuberculosis H37Rv PknF kinase domain
20216VXUStructure of Human Vaccinia-related Kinase 1 (VRK1) bound to ACH471
20206W3ZCrystal Structure of Brugia malayi Deoxyhypusine synthase (DHPS)
20206VXRStructure of Maternal embryonic leucine zipper kinase bound to LDSM276
20206VXHStructure of ABCG2 bound to imatinib
20196PJJHuman PRPF4B bound to benzothiophene inhibitor 224
20196PK6Human PRPF4B bound to benzothiophene inhibitor 329
20196PCWHuman PIM1 bound to benzothiophene inhibitor 213
20196PDIHuman PIM1 bound to benzothiophene inhibitor 224
20196PDNHuman PIM1 bound to benzothiophene inhibitor 292
20196PDOHuman PIM1 bound to benzothiophene inhibitor 354
20196PDPHuman PIM1 bound to benzothiophene inhibitor 379
20196NPNCrystal Structure of the Human vaccinia-related kinase bound to a N,N-dipropynyl-dihydropteridine-3-hydroxyindazole inhibitor
20196NCGCrystal Structure of Human Vaccinia-related kinase 2 (VRK-2) bound to pyridin-benzenesulfonamide inhibitor
20186EASCo-crystal of pseudokinase DRIK1 (drought responsive inactive kinase 1) bound to ENMD-2076
20185WAXCrystal Structure of Sugarcane SAPK10 (serine/threonine-protein kinase 10)
20186DD4Crystal Structure of the Human vaccinia-related kinase bound to a N,N-dipropyl-dihydropteridine inhibitor
20186CTHCrystal Structure of Pathogenesis-related Protein 1G (PR-1G) Kinase Domain from Cacao
20186CNXCrystal Structure of the Human vaccinia-related kinase 1 (VRK1) bound to an N-propynyl-N-isopentyl-dihydropteridin inhibitor
20186CPYStructure of apo GRMZM2G135359 pseudokinase
20186CSWCrystal Structure of the Human vaccinia-related kinase bound to a N-methyl-N-propyl-dihydropteridine inhibitor
20186CNHHuman PRPF4B in complex with Rebastinib
20186CMMCrystal Structure of the Human vaccinia-related kinase bound to a N,N-dipropynyl-dihydropteridine inhibitor
20186CQHCrystal Structure of the Human vaccinia-related kinase bound to a N-propynyl-N-ethyl-dihydropteridine inhibitor
20186CQHCrystal Structure of the Human vaccinia-related kinase bound to a N-propynyl-N-ethyl-dihydropteridine inhibitor.
20186CCFCrystal Structure of the Human CAMKK1A in complex with Hesperadin.
20186CD6Crystal Structure of the Human CAMKK1A in complex with GSK650394.
20186CFMCrystal Structure of the Human vaccinia-related kinase bound to a propynyl-pteridinone inhibitor.
20176BTWCrystal Structure of the Human vaccinia-related kinase bound to a phenyl-pteridinone inhibitor.
20176BU6Crystal Structure of the Human vaccinia-related kinase bound to a bis-difluorophenol-aminopyridine inhibitor.
20176BQLCrystal Structure of the Human CAMKK2B in complex with TAE-226.
20176BQPCrystal Structure of the Human CAMKK2B in complex with Crenolanib.
20176BQQCrystal Structure of the Human CAMKK2B in complex with BI2526.
20176BRCCrystal Structure of the Human CAMKK2B in complex with AP26113-analog (ALK-IN-1).
20176BRUCrystal Structure of the Human vaccinia-related kinase bound to a (S)-2-phenylaminopteridinone inhibitor.
20176BP0Crystal Structure of the Human vaccinia-related kinase 1 bound to (R)-2-phenylaminopteridinone inhibitor.
20176BKUCrystal Structure of the Human CAMKK2B bound to GSK650394.
20176BLECrystal Structure of the Human CAMKK2B in complex with CP673451.
20175VT1Crystal Structure of the Human CAMKK2B bound to a thiadiazinone benzamide inhibitor.