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Crystal Structure of the MerTK Kinase Domain in Complex with Inhibitor MIPS15692[SIGNALING PROTEIN/INHIBITOR]
View in iCn3D PubMedProteinsConserved DomainsPubChem Compound
CRYSTAL STRUCTURE OF AP2 ASSOCIATED KINASE 1 COMPLEXED WITH (5P)-3-({(8R)-5-[(4-aminopiperidin-1-yl)methyl]pyrrolo[2,1-f][1,2,4]triazin-4-yl}amino)-5-[2-(propan-2-yl)-2H-tetrazol-5-yl]phenol[TRANSFERA...
View in iCn3D Similar StructuresPubMedProteinsPubChem Compound
CRYSTAL STRUCTURE OF AP2 ASSOCIATED KINASE 1 COMPLEXED WITH 5-[(4-aminopiperidin-1-yl)methyl]-N-{3-[5-(propan-2-yl)-1,3,4-thiadiazol-2-yl]phenyl}pyrrolo[2,1-f][1,2,4]triazin-4-amine[TRANSFERASE]
Crystal structure of AcAChBP in complex with anatoxin[SIGNALING PROTEIN]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Crystal structure of AcAChBP in complex with hosieine[SIGNALING PROTEIN]
Crystal structure of rat cyclophilin D in complex with a potent nonimmunosuppressive inhibitor[ISOMERASE/ISOMERASE Inhibitor]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
THE STRUCTURE OF OMPF PORIN IN A TETRAGONAL CRYSTAL FORM[MEMBRANE PROTEIN]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
Gly156Asp mutant of Human UroD, human uroporphyrinogen III decarboxylase[LYASE]
Phe232Leu mutant of human UROD, human uroporphyrinogen III decarboxylase[LYASE]
Ile260Thr mutant of Human UroD, human uroporphyrinogen III decarboxylase[LYASE]
BRD4-D1 in complex with BET inhibitor[GENE REGULATION/INHIBITOR]
BRD4-D1 in complex with BET inhibitor[GENE REGULATION]
Structure of the beta-ketoacyl reductase domain of human fatty acid synthase bound to a spiro-imidazolone inhibitor[OXIDOREDUCTASE/OXIDOREDUCTASE Inhibitor]
Structure Of Bace Bound To (R)-5-Cyclopropyl-2-Imino-3-Methyl-5-(3-(5- (Prop-1-Yn-1-Yl)pyridin-3-Yl)phenyl)imidazolidin-4-One[HydrolaseHYDROLASE INHIBITOR, EC: 3.4.23.46]
Structure Of Bace Bound To 5-(3-(5-Chloropyridin-3-Yl)phenyl)-5- Cyclopropyl-2-Imino-3-Methylimidazolidin-4-One[HydrolaseHYDROLASE INHIBITOR, EC: 3.4.23.46]
Structure Of Bace Bound To 2-Imino-3-Methyl-5-Phenyl-5-(3-(Pyridin-3- Yl)phenyl)imidazolidin-4-One[HydrolaseHYDROLASE INHIBITOR, EC: 3.4.23.46]
Structure of BACE Bound to 2-imino-5-(3'-methoxy-[1,1'-biphenyl]-3-yl)-3-methyl-5-phenylimidazolidin-4-one[HYDROLASE/HYDROLASE INHIBITOR]
Structure Of Bace Bound To 2-Imino-3-Methyl-5,5-Diphenylimidazolidin- 4-One[HydrolaseHYDROLASE INHIBITOR, EC: 3.4.23.46]
Solution Structure of GIP(1-30)amide in TFE/Water[HORMONE/GROWTH FACTOR]
View in iCn3D PubMedProteinsConserved Domains
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