{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]P08581,1,P08581,12,2]["},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"P08581","source":"P08581|Hepatocyte growth factor receptor","targets":["1FYR|DIMER FORMATION THROUGH DOMAIN SWAPPING IN THE CRYSTAL STRUCTURE OF THE GRB2-SH2 AC-PYVNV COMPLEX|X-RAY DIFFRACTION|2.4|Homo sapiens; SYNTHETIC CONSTRUCT|0|HORMONE/GROWTH FACTOR","1R0P|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-Met in complex with the microbial alkaloid K-252a|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE","1R1W|CRYSTAL STRUCTURE OF THE TYROSINE KINASE DOMAIN OF THE HEPATOCYTE GROWTH FACTOR RECEPTOR C-MET|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE","1SHY|The Crystal Structure of HGF beta-chain in Complex with the Sema Domain of the Met Receptor.|X-RAY DIFFRACTION|3.22|Homo sapiens|0|GROWTH FACTOR/GROWTH FACTOR RECEPTOR","1SSL|Solution structure of the PSI domain from the Met receptor|SOLUTION NMR||Homo sapiens|0|STRUCTURAL PROTEIN","2G15|Structural Characterization of autoinhibited c-Met kinase|X-RAY DIFFRACTION|2.15|Homo sapiens|0|TRANSFERASE","2RFN|x-ray structure of c-Met with inhibitor.|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE","2RFS|X-ray structure of SU11274 bound to c-Met|X-RAY DIFFRACTION|2.2|Homo sapiens|0|TRANSFERASE","2UZX|Structure of the human receptor tyrosine kinase Met in complex with the Listeria monocytogenes invasion protein InlB: Crystal form I|X-RAY DIFFRACTION|2.8|HOMO SAPIENS; LISTERIA MONOCYTOGENES|0|SIGNALING PROTEIN/RECEPTOR","2UZY|Structure of the human receptor tyrosine kinase Met in complex with the Listeria monocytogenes invasion protein inlb: low resolution, Crystal form II|X-RAY DIFFRACTION|4|HOMO SAPIENS; LISTERIA MONOCYTOGENES|0|SIGNALING PROTEIN/RECEPTOR","2WD1|Human c-Met Kinase in complex with azaindole inhibitor|X-RAY DIFFRACTION|2|HOMO SAPIENS|0|TRANSFERASE","2WGJ|X-ray Structure of PF-02341066 bound to the kinase domain of c-Met|X-RAY DIFFRACTION|2|HOMO SAPIENS|0|TRANSFERASE","2WKM|X-ray Structure of PHA-00665752 bound to the kinase domain of c-Met|X-RAY DIFFRACTION|2.2|HOMO SAPIENS|0|TRANSFERASE","3A4P|human c-MET kinase domain complexed with 6-benzyloxyquinoline inhibitor|X-RAY DIFFRACTION|2.54|Homo sapiens|0|TRANSFERASE","3BUX|Crystal structure of c-Cbl-TKB domain complexed with its binding motif in c-Met|X-RAY DIFFRACTION|1.35|Homo sapiens; SYNTHETIC CONSTRUCT|0|LIGASE/SIGNALING PROTEIN","3C1X|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-MET in complex with a Pyrrolotriazine based inhibitor|X-RAY DIFFRACTION|2.17|Homo sapiens|0|TRANSFERASE","3CCN|X-ray structure of c-Met with triazolopyridazine inhibitor.|X-RAY DIFFRACTION|1.9|Homo sapiens|0|TRANSFERASE","3CD8|X-ray Structure of c-Met with triazolopyridazine Inhibitor.|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE","3CE3|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor C-MET in complex with a Pyrrolopyridinepyridone based inhibitor|X-RAY DIFFRACTION|2.4|Homo sapiens|0|TRANSFERASE","3CTH|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a aminopyridine based inhibitor|X-RAY DIFFRACTION|2.3|Homo sapiens|0|TRANSFERASE","3CTJ|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor c-met in complex with a aminopyridine based inhibitor|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE","3DKC|Structure of MET receptor tyrosine kinase in complex with ATP|X-RAY DIFFRACTION|1.52|Homo sapiens|0|ONCOPROTEIN","3DKF|Structure of MET receptor tyrosine kinase in complex with inhibitor SGX-523|X-RAY DIFFRACTION|1.8|Homo sapiens|0|ONCOPROTEIN","3DKG|Structure of Mutant(Y1248L) MET receptor tyrosine kinase in complex with inhibitor SGX-523|X-RAY DIFFRACTION|1.91|Homo sapiens|0|ONCOPROTEIN","3EFJ|Structure of c-Met with pyrimidone inhibitor 7|X-RAY DIFFRACTION|2.6|Homo sapiens|0|TRANSFERASE","3EFK|Structure of c-Met with pyrimidone inhibitor 50|X-RAY DIFFRACTION|2.2|Homo sapiens|0|TRANSFERASE","3F66|Human c-Met Kinase in complex with quinoxaline inhibitor|X-RAY DIFFRACTION|1.4|Homo sapiens|0|TRANSFERASE","3F82|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor C-MET in complex with N-(4-(2-amino-3-chloropyridin-4-yloxy)-3-fluorophenyl)-4-ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE","3I5N|Crystal structure of c-Met with triazolopyridazine inhibitor 13|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE","3L8V|Crystal structure of the tyrosine kinase domain of the hepatocyte growth factor receptor C-MET in complex with a biarylamine based inhibitor|X-RAY DIFFRACTION|2.4|Homo sapiens|0|TRANSFERASE","3LQ8|Structure of the kinase domain of c-Met bound to XL880 (GSK1363089)|X-RAY DIFFRACTION|2.02|Homo sapiens|0|TRANSFERASE","3Q6U|Structure of the apo MET receptor kinase in the dually-phosphorylated, activated state|X-RAY DIFFRACTION|1.6|Homo sapiens|0|TRANSFERASE","3Q6W|Structure of dually-phosphorylated MET receptor kinase in complex with an MK-2461 analog with specificity for the activated receptor|X-RAY DIFFRACTION|1.75|Homo sapiens|0|transferase/transferase inhibitor","3QTI|c-Met Kinase in Complex with NVP-BVU972|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3R7O|Structure of dually phosphorylated c-MET receptor kinase in complex with an MK-2461 analog|X-RAY DIFFRACTION|2.3|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3RHK|Crystal structure of the catalytic domain of c-Met kinase in complex with ARQ 197|X-RAY DIFFRACTION|1.94|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3U6H|Crystal structure of c-Met in complex with pyrazolone inhibitor 26|X-RAY DIFFRACTION|2|Homo sapiens|0|transferase/transferase inhibitor","3U6I|Crystal structure of c-Met in complex with pyrazolone inhibitor 58a|X-RAY DIFFRACTION|2.1|Homo sapiens|0|transferase/transferase inhibitor","3VW8|Crystal structure of human c-Met kinase domain with its inhibitor|X-RAY DIFFRACTION|2.1|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3ZBX|X-ray Structure of c-Met kinase in complex with inhibitor 6-((6-(4- fluorophenyl)-(1,2,4)triazolo(4,3-b)(1,2,4)triazin-3-yl)methyl) quinoline.|X-RAY DIFFRACTION|2.2|HOMO SAPIENS|0|TRANSFERASE","3ZC5|X-ray Structure of c-Met kinase in complex with inhibitor (S)-6-(1-(6- (1-methyl-1H-pyrazol-4-yl)-(1,2,4)triazolo(4,3-b)pyridazin-3-yl)ethyl) quinoline.|X-RAY DIFFRACTION|2.2|HOMO SAPIENS|0|TRANSFERASE","3ZCL|X-ray Structure of c-Met kinase in complex with inhibitor (S)-3-(1-(1H-pyrrolo(2,3-b)pyridin-3-yl)ethyl)-N-isopropyl-(1,2,4)triazolo(4,3- b)pyridazin-6-amine|X-RAY DIFFRACTION|1.4|HOMO SAPIENS|0|TRANSFERASE","3ZXZ|X-ray Structure of PF-04217903 bound to the kinase domain of c-Met|X-RAY DIFFRACTION|1.8|HOMO SAPIENS|0|TRANSFERASE","3ZZE|Crystal structure of C-MET kinase domain in complex with N'-((3Z)-4- chloro-7-methyl-2-oxo-1,2-dihydro-3H-indol-3-ylidene)-2-(4- hydroxyphenyl)propanohydrazide|X-RAY DIFFRACTION|1.87|HOMO SAPIENS|0|TRANSFERASE","4AOI|Crystal structure of C-MET kinase domain in complex with 4-(3-((1H- pyrrolo(2,3-b)pyridin-3-yl)methyl)-(1,2,4)triazolo(4,3-b)(1,2,4) triazin-6-yl)benzonitrile|X-RAY DIFFRACTION|1.9|HOMO SAPIENS|0|TRANSFERASE","4AP7|Crystal structure of C-MET kinase domain in complex with 4-((6-(4- fluorophenyl)-(1,2,4)triazolo(4,3-b)(1,2,4)triazin-3-yl)methyl)phenol|X-RAY DIFFRACTION|1.8|HOMO SAPIENS|0|TRANSFERASE","4DEG|Crystal structure of c-Met in complex with triazolopyridazine inhibitor 2|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4DEH|Crystal structure of c-Met in complex with triazolopyridinone inhibitor 3|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4DEI|Crystal structure of c-Met in complex with triazolopyridinone inhibitor 24|X-RAY DIFFRACTION|2.05|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4EEV|Crystal structure of c-Met in complex with LY2801653|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4GG5|Crystal structure of CMET in complex with novel inhibitor|X-RAY DIFFRACTION|2.423|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4GG7|Crystal structure of cMET in complex with novel inhibitor|X-RAY DIFFRACTION|2.27|Homo sapiens|0|Transferase/Transferase inhibitor","4IWD|Structure of dually phosphorylated c-MET receptor kinase in complex with an MK-8033 analog|X-RAY DIFFRACTION|1.99|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4K3J|Crystal structure of Onartuzumab Fab in complex with MET and HGF-beta|X-RAY DIFFRACTION|2.8|Homo sapiens; Mus musculus, Homo sapiens|0|Transferase/Immune System/Growth Factor","4KNB|C-Met in complex with OSI ligand|X-RAY DIFFRACTION|2.4|Homo sapiens|0|TRANSFERASE","4MXC|Crystal structure of CMET in complex with novel inhibitor|X-RAY DIFFRACTION|1.632|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4O3T|Zymogen HGF-beta/MET with Zymogen Activator Peptide ZAP.14|X-RAY DIFFRACTION|2.99|Homo sapiens; SYNTHETIC CONSTRUCT|0|transferase/growth factor","4O3U|Zymogen HGF-beta/MET with Zymogen Activator Peptide ZAP2.3|X-RAY DIFFRACTION|3.04|Homo sapiens; SYNTHETIC CONSTRUCT|0|transferase/growth factor","4R1V|Identification and optimization of pyridazinones as potent and selective c-Met kinase inhibitors|X-RAY DIFFRACTION|1.2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4R1Y|Identification and optimization of pyridazinones as potent and selective c-Met kinase inhibitor|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4XMO|Crystal structure of c-Met in complex with (R)-5-(8-fluoro-3-(1-fluoro-1-(3-methoxyquinolin-6-yl)ethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-3-methylisoxazole|X-RAY DIFFRACTION|1.75|Homo sapiens|0|Transferase/transferase inhibitor","4XYF|Crystal structure of c-Met in complex with (S)-5-(8-fluoro-3-(1-(3-(2-methoxyethoxy)quinolin-6-yl)ethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-3-methylisoxazole|X-RAY DIFFRACTION|1.85|Homo sapiens|0|TRANSFERASE/TRANSFERASE Inhibitor","5DG5|CRYSTAL STRUCTURE OF THE TYROSINE KINASE DOMAIN OF THE HEPATOCYTE GROWTH FACTOR RECEPTOR C-MET IN COMPLEX WITH ALTIRATINIB ANALOG DP-4157|X-RAY DIFFRACTION|2.6|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5EOB|Crystal structure of CMET in complex with novel inhibitor|X-RAY DIFFRACTION|1.75|Homo sapiens|0|TRANSFERASE","5EYC|Crystal structure of c-Met in complex with naphthyridinone inhibitor 5|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5EYD|Crystal structure of c-Met in complex with AMG 337|X-RAY DIFFRACTION|1.85|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5HLW|Crystal structure of c-Met mutant Y1230H in complex with compound 14|X-RAY DIFFRACTION|1.97|Homo sapiens|0|TRANSFERASE","5HNI|CRYSTAL STRUCTURE OF CMET WT with compound 3|X-RAY DIFFRACTION|1.71|Homo sapiens|0|TRANSFERASE","5HO6|CRYSTAL STRUCTURE OF CMET IN COMPLEX WITH CMPD.|X-RAY DIFFRACTION|1.97|Homo sapiens|0|TRANSFERASE","5HOA|Crystal structure of c-Met L1195V in complex with SAR125844|X-RAY DIFFRACTION|2.14|Homo sapiens|0|TRANSFERASE","5HOR|Crystal structure of c-Met-M1250T in complex with SAR125844.|X-RAY DIFFRACTION|2.2|Homo sapiens|0|TRANSFERASE","5HTI|Crystal structure of c-Met kinase domain in complex with LXM108|X-RAY DIFFRACTION|1.66|Homo sapiens|0|TRANSFERASE","5LSP|107_A07 Fab in complex with fragment of the Met receptor|X-RAY DIFFRACTION|2.605|Homo sapiens|0|TRANSFERASE","5T3Q|Crystal structure of the c-Met kinase domain in complex with a pyrazolone inhibitor|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5UAB|MET Tyrosine Kinase Inhibition Enhances the Antitumor Efficacy of an HGF Antibody|X-RAY DIFFRACTION|1.9|Homo sapiens|0|TRANSFERASE/INHIBITOR","5UAD|MET Tyrosine Kinase Inhibition Enhances the Antitumor Efficacy of an HGF Antibody|X-RAY DIFFRACTION|2.25|Homo sapiens|0|TRANSFERASE/INHIBITOR","5YA5|CRYSTAL STRUCTURE OF c-MET IN COMPLEX WITH NOVEL INHIBITOR|X-RAY DIFFRACTION|1.89|Homo sapiens|0|TRANSFERASE/INHIBITOR","6GCU|MET receptor in complex with InlB internalin domain and DARPin A3A|X-RAY DIFFRACTION|6.001|Homo sapiens; Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e); synthetic construct|0|SIGNALING PROTEIN","6I04|Crystal structure of Sema domain of the Met receptor in complex with FAB|X-RAY DIFFRACTION|3.1|Homo sapiens|0|IMMUNE SYSTEM","6SD9|Crystal structure of wild-type cMET bound by foretinib|X-RAY DIFFRACTION|2.35|Homo sapiens|0|TRANSFERASE","6SDC|Crystal structure of D1228V cMET bound by foretinib|X-RAY DIFFRACTION|1.67|Homo sapiens|0|TRANSFERASE","6SDD|Crystal structure of D1228V cMET bound by BMS-777607|X-RAY DIFFRACTION|1.93|Homo sapiens|0|TRANSFERASE","6SDE|Crystal structure of wild-type cMET bound by savolitinib|X-RAY DIFFRACTION|2.49|Homo sapiens|0|TRANSFERASE","6UBW|MET Tyrosine Kinase Inhibition Enhances the Antitumor Efficacy of an HGF Antibody|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE-TRANSFERASE INHIBITOR","6WVZ|Crystal structure of anti-MET Fab arm of amivantamab in complex with human MET|X-RAY DIFFRACTION|3.1|Homo sapiens|0|Transferase/Immune System","7B3Q|Crystal structure of c-MET bound by compound 1|X-RAY DIFFRACTION|1.75|Homo sapiens|0|TRANSFERASE","7B3T|Crystal structure of c-MET bound by compound 2|X-RAY DIFFRACTION|2.23|Homo sapiens|0|TRANSFERASE","7B3V|Crystal structure of c-MET bound by compound 3|X-RAY DIFFRACTION|1.93|Homo sapiens|0|TRANSFERASE","7B3W|Crystal structure of c-MET bound by compound 4|X-RAY DIFFRACTION|2.02|Homo sapiens|0|TRANSFERASE","7B3Z|Crystal structure of c-MET bound by compound 5|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE","7B40|Crystal structure of c-MET bound by compound 6|X-RAY DIFFRACTION|1.76|Homo sapiens|0|TRANSFERASE","7B41|Crystal structure of c-MET bound by compound 7|X-RAY DIFFRACTION|1.97|Homo sapiens|0|TRANSFERASE","7B42|Crystal structure of c-MET bound by compound 8|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE","7B43|Crystal structure of c-MET bound by compound 9|X-RAY DIFFRACTION|1.87|Homo sapiens|0|TRANSFERASE","7B44|Crystal structure of c-MET bound by compound S1|X-RAY DIFFRACTION|1.76|Homo sapiens|0|TRANSFERASE","7MO7|Cryo-EM structure of 2:2 c-MET/HGF holo-complex|ELECTRON MICROSCOPY|4.8|Homo sapiens|0|SIGNALING PROTEIN","7MO8|Cryo-EM structure of 1:1 c-MET I/HGF I complex after focused 3D refinement of holo-complex|ELECTRON MICROSCOPY|4.5|Homo sapiens|0|SIGNALING PROTEIN","7MO9|Cryo-EM map of the c-MET II/HGF I/HGF II (K4 and SPH) sub-complex|ELECTRON MICROSCOPY|4.0|Homo sapiens|0|SIGNALING PROTEIN","7MOA|Cryo-EM structure of the c-MET II/HGF I complex bound with HGF II in a rigid conformation|ELECTRON MICROSCOPY|4.9|Homo sapiens|0|SIGNALING PROTEIN","7MOB|Cryo-EM structure of 2:2 c-MET/NK1 complex|ELECTRON MICROSCOPY|5.0|Homo sapiens|0|SIGNALING PROTEIN"]}]}