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Human Dyrk1aHARMINE COMPLEX[TransferaseTRANSFERASE INHIBITOR, EC: 2.7.12.1]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
human DYRK1A/inhibitor complex[TRANSFERASE/TRANSFERASE INHIBITOR]
Crystal structure of human CLK1 in complex with 10Z-Hymenialdisine[TRANSFERASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsBioAssay
Crystal structure of di-phosphorylated human CLK1 in complex with a novel substituted indole inhibitor[TRANSFERASE]
Crystal structure of SR protein kinase 1 complexed to its substrate ASF/SF2[Transferase/Splicing]
Structure of human serine-arginine-rich protein-specific kinase 2 (SRPK2) bound to purvalanol B[TRANSFERASE]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
JNK3 bound to piperazine amide inhibitor, SR2774[TRANSFERASE]
Crystal structure of JNK3 with indazole inhibitor, SR-3737[TRANSFERASE]
Crystal Structure of JNK2[TRANSFERASE]
JNK3 bound to aminopyrimidine inhibitor, SR-3562[TRANSFERASE]
Crystal structure of JNK3 with amino-pyrazole inhibitor, SR-3451[TRANSFERASE]
c-Jun N-terminal Kinase 3 with 3,5-Disubstituted Quinoline inhibitor[SIGNALING PROTEIN, TRANSFERASE]
Crystal structure of JNK2 complexed with BIRB796[TRANSFERASE/TRANSFERASE INHIBITOR]
JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-styrylindolin-2-one[TRANSFERASE]
JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-phenylindolin-2-one[TRANSFERASE]
JNK-3 bound to (Z)-5-fluoro-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)indolin-2-one[TRANSFERASE]
IRAK-4 Inhibitors (Part II)- A structure based assessment of imidazo[1,2 a]pyridine binding[TRANSFERASE]
Synthesis and SAR of Aminopyrimidines as Novel c-Jun N-Terminal Kinase (JNK) Inhibitors[TRANSFERASE]
Crystal structure of JNK3 bound to N-benzyl-4-(4-(3-chlorophenyl)-1H-pyrazol-3-yl)-1H-pyrrole-2-carboxamide[TRANSFERASE]
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