{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":1,"total":34,"mapped":1},"pagination":{"has_next":false},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"P07949","source":"P07949|Proto-oncogene tyrosine-protein kinase receptor Ret","targets":["2IVS|Crystal structure of non-phosphorylated RET tyrosine kinase domain|X-RAY DIFFRACTION|2|HOMO SAPIENS|0|TRANSFERASE","2IVT|Crystal structure of phosphorylated RET tyrosine kinase domain|X-RAY DIFFRACTION|2.6|HOMO SAPIENS|0|TRANSFERASE","2IVU|Crystal structure of phosphorylated RET tyrosine kinase domain complexed with the inhibitor ZD6474|X-RAY DIFFRACTION|2.5|HOMO SAPIENS|0|TRANSFERASE","2IVV|Crystal structure of phosphorylated RET tyrosine kinase domain complexed with the inhibitor PP1|X-RAY DIFFRACTION|2.25|HOMO SAPIENS|0|TRANSFERASE","2X2K|Crystal Structure of phosphorylated RET tyrosine kinase domain with inhibitor|X-RAY DIFFRACTION|2.6|HOMO SAPIENS|0|TRANSFERASE","2X2L|Crystal Structure of phosphorylated RET tyrosine kinase domain with inhibitor|X-RAY DIFFRACTION|2|HOMO SAPIENS|0|TRANSFERASE","2X2M|Crystal Structure of phosphorylated RET tyrosine kinase domain with inhibitor|X-RAY DIFFRACTION|2.5|HOMO SAPIENS|0|TRANSFERASE","2X2U|First two Cadherin-like domains from Human RET|X-RAY DIFFRACTION|2|HOMO SAPIENS|0|TRANSFERASE","4CKI|Crystal Structure of oncogenic RET tyrosine kinase M918T bound to adenosine|X-RAY DIFFRACTION|2.116|HOMO SAPIENS|0|TRANSFERASE","4CKJ|Crystal structure of RET tyrosine kinase domain bound to adenosine|X-RAY DIFFRACTION|1.65|HOMO SAPIENS|0|TRANSFERASE","4UX8|RET recognition of GDNF-GFRalpha1 ligand by a composite binding site promotes membrane-proximal self-association|ELECTRON MICROSCOPY|24.0|HOMO SAPIENS; RATTUS NORVEGICUS|0|SIGNALING PROTEIN","5AMN|The Discovery of 2-Substituted Phenol Quinazolines as Potent and Selective RET Kinase Inhibitors|X-RAY DIFFRACTION|2.57|HOMO SAPIENS|0|TRANSFERASE","5FM2|Crystal structure of hyper-phosphorylated RET kinase domain with (proximal) juxtamembrane segment|X-RAY DIFFRACTION|3.3|HOMO SAPIENS|0|TRANSFERASE","5FM3|Crystal structure of hyper-phosphorylated RET kinase domain with (proximal) juxtamembrane segment|X-RAY DIFFRACTION|2.95|HOMO SAPIENS|0|TRANSFERASE","6FEK|Oncogenic point mutation of RET receptor tyrosine kinase|X-RAY DIFFRACTION|2.3|Homo sapiens|0|ONCOPROTEIN","6GL7|Neurturin-GFRa2-RET extracellular complex|ELECTRON MICROSCOPY|6.3|Homo sapiens|0|SIGNALING PROTEIN","6I82|Crystal structure of partially phosphorylated RET V804M tyrosine kinase domain complexed with PDD00018412|X-RAY DIFFRACTION|2.05|Homo sapiens|0|ONCOPROTEIN","6I83|Crystal structure of phosphorylated RET V804M tyrosine kinase domain complexed with PDD00018366|X-RAY DIFFRACTION|1.88|Homo sapiens|0|ONCOPROTEIN","6NE7|Structure of G810A mutant of RET protein tyrosine kinase domain.|X-RAY DIFFRACTION|1.99|Homo sapiens|0|TRANSFERASE","6NEC|STRUCTURE OF RET PROTEIN TYROSINE KINASE DOMAIN IN COMPLEX WITH NINTEDANIB|X-RAY DIFFRACTION|1.87|Homo sapiens|0|TRANSFERASE","6NJA|Structure of WT RET protein tyrosine kinase domain at 1.92A resolution.|X-RAY DIFFRACTION|1.92|Homo sapiens|0|TRANSFERASE","6Q2J|Cryo-EM structure of extracellular dimeric complex of RET/GFRAL/GDF15|ELECTRON MICROSCOPY|4.1|Homo sapiens|0|SIGNALING PROTEIN","6Q2N|Cryo-EM structure of RET/GFRa1/GDNF extracellular complex|ELECTRON MICROSCOPY|4.4|Homo sapiens|0|SIGNALING PROTEIN","6Q2O|Cryo-EM structure of RET/GFRa2/NRTN extracellular complex. The 3D refinement was applied with C2 symmetry.|ELECTRON MICROSCOPY|3.65|Homo sapiens|0|SIGNALING PROTEIN","6Q2R|Cryo-EM structure of RET/GFRa2/NRTN extracellular complex in the tetrameric form|ELECTRON MICROSCOPY|4.3|Homo sapiens|0|SIGNALING PROTEIN","6Q2S|Cryo-EM structure of RET/GFRa3/ARTN extracellular complex. The 3D refinement was applied with C2 symmetry.|ELECTRON MICROSCOPY|3.8|Homo sapiens; Saccharomyces cerevisiae|0|SIGNALING PROTEIN","6VHG|Crystal structure of phosphorylated RET tyrosine kinase domain complexed with a pyrazolo[1,5-a]pyrimidine inhibitor|X-RAY DIFFRACTION|2.303|Homo sapiens|0|Transferase/Transferase Inhibitor","7DU8|Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with Selpercatinib|X-RAY DIFFRACTION|2.75|Homo sapiens|0|TRANSFERASE","7DU9|Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with Pralsetinib|X-RAY DIFFRACTION|2.31|Homo sapiens|0|TRANSFERASE","7DUA|Crystal structure of human Proto-oncogene tyrosine-protein kinase receptor Ret in complex with 4-amino-7-(1-methylcyclopropyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[2,3-d]pyrimidine-5-carboxamide|X-RAY DIFFRACTION|1.64|Homo sapiens|0|TRANSFERASE","7JU5|Structure of RET protein tyrosine kinase in complex with pralsetinib|X-RAY DIFFRACTION|1.9|Homo sapiens|0|Transferase/Transferase inhibitor","7JU6|Structure of RET protein tyrosine kinase in complex with selpercatinib|X-RAY DIFFRACTION|2.06|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","7NZN|Structure of RET kinase domain bound to inhibitor JB-48|X-RAY DIFFRACTION|2.39|Homo sapiens|0|TRANSFERASE","7RUN|Crystal structure of phosphorylated RET tyrosine kinase domain complexed with a pyrrolo[2,3-d]pyrimidine inhibitor.|X-RAY DIFFRACTION|3.51|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR"]}]}