{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]P00533,1,P00533,16,3]["},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"P00533","source":"P00533|Epidermal growth factor receptor","targets":["1IVO|Crystal Structure of the Complex of Human Epidermal Growth Factor and Receptor Extracellular Domains.|X-RAY DIFFRACTION|3.3|Homo sapiens|0|TRANSFERASE/SIGNALING PROTEIN","1M14|Tyrosine Kinase Domain from Epidermal Growth Factor Receptor|X-RAY DIFFRACTION|2.6|Homo sapiens|0|TRANSFERASE","1M17|Epidermal Growth Factor Receptor tyrosine kinase domain with 4-anilinoquinazoline inhibitor erlotinib|X-RAY DIFFRACTION|2.6|Homo sapiens|0|TRANSFERASE","1MOX|Crystal Structure of Human Epidermal Growth Factor Receptor (residues 1-501) in complex with TGF-alpha|X-RAY DIFFRACTION|2.5|Homo sapiens|0|transferase/growth factor","1NQL|Structure of the extracellular domain of human epidermal growth factor (EGF) receptor in an inactive (low pH) complex with EGF.|X-RAY DIFFRACTION|2.8|Homo sapiens|0|HORMONE/GROWTH FACTOR RECEPTOR","1XKK|EGFR kinase domain complexed with a quinazoline inhibitor- GW572016|X-RAY DIFFRACTION|2.4|Homo sapiens|0|TRANSFERASE","1YY9|Structure of the extracellular domain of the epidermal growth factor receptor in complex with the Fab fragment of cetuximab/Erbitux/IMC-C225|X-RAY DIFFRACTION|2.605|Homo sapiens; Mus musculus, Homo sapiens|0|IMMUNE SYSTEM/Transferase","1Z9I|A Structural Model for the Membrane-Bound Form of the Juxtamembrane Domain of the Epidermal Growth Factor Receptor|SOLUTION NMR||Homo sapiens|0|TRANSFERASE","2EB2|Crystal structure of mutated EGFR kinase domain (G719S)|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE","2EB3|Crystal structure of mutated EGFR kinase domain (L858R) in complex with AMPPNP|X-RAY DIFFRACTION|2.84|Homo sapiens|0|TRANSFERASE","2GS2|Crystal Structure of the active EGFR kinase domain|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE","2GS6|Crystal Structure of the active EGFR kinase domain in complex with an ATP analog-peptide conjugate|X-RAY DIFFRACTION|2.6|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSFERASE","2GS7|Crystal Structure of the inactive EGFR kinase domain in complex with AMP-PNP|X-RAY DIFFRACTION|2.6|Homo sapiens|0|TRANSFERASE","2ITN|Crystal structure of EGFR kinase domain G719S mutation in complex with AMP-PNP|X-RAY DIFFRACTION|2.47|HOMO SAPIENS|0|TRANSFERASE","2ITO|Crystal structure of EGFR kinase domain G719S mutation in complex with Iressa|X-RAY DIFFRACTION|3.25|HOMO SAPIENS|0|TRANSFERASE","2ITP|Crystal structure of EGFR kinase domain G719S mutation in complex with AEE788|X-RAY DIFFRACTION|2.74|HOMO SAPIENS|0|TRANSFERASE","2ITQ|Crystal structure of EGFR kinase domain G719S mutation in complex with AFN941|X-RAY DIFFRACTION|2.68|HOMO SAPIENS|0|TRANSFERASE","2ITT|Crystal structure of EGFR kinase domain L858R mutation in complex with AEE788|X-RAY DIFFRACTION|2.73|HOMO SAPIENS|0|TRANSFERASE","2ITU|Crystal structure of EGFR kinase domain L858R mutation in complex with AFN941|X-RAY DIFFRACTION|2.8|HOMO SAPIENS|0|TRANSFERASE","2ITV|Crystal structure of EGFR kinase domain L858R mutation in complex with AMP-PNP|X-RAY DIFFRACTION|2.47|HOMO SAPIENS|0|TRANSFERASE","2ITW|Crystal structure of EGFR kinase domain in complex with AFN941|X-RAY DIFFRACTION|2.88|HOMO SAPIENS|0|TRANSFERASE","2ITX|Crystal structure of EGFR kinase domain in complex with AMP-PNP|X-RAY DIFFRACTION|2.98|HOMO SAPIENS|0|TRANSFERASE","2ITY|Crystal structure of EGFR kinase domain in complex with Iressa|X-RAY DIFFRACTION|3.42|HOMO SAPIENS|0|TRANSFERASE","2ITZ|Crystal structure of EGFR kinase domain L858R mutation in complex with Iressa|X-RAY DIFFRACTION|2.8|HOMO SAPIENS|0|TRANSFERASE","2J5E|Crystal structure of EGFR kinase domain in complex with an irreversible inhibitor 13-jab|X-RAY DIFFRACTION|3.1|HOMO SAPIENS|0|TRANSFERASE","2J5F|Crystal structure of EGFR kinase domain in complex with an irreversible inhibitor 34-jab|X-RAY DIFFRACTION|3|HOMO SAPIENS|0|TRANSFERASE","2J6M|Crystal structure of EGFR kinase domain in complex with AEE788|X-RAY DIFFRACTION|3.1|HOMO SAPIENS|0|TRANSFERASE","2JIT|Crystal structure of EGFR kinase domain T790M mutation|X-RAY DIFFRACTION|3.1|HOMO SAPIENS|0|TRANSFERASE","2JIU|Crystal structure of EGFR kinase domain T790M mutation in complex with AEE788|X-RAY DIFFRACTION|3.05|HOMO SAPIENS|0|TRANSFERASE","2JIV|Crystal structure of EGFR kinase domain T790M mutation in compex with HKI-272|X-RAY DIFFRACTION|3.5|HOMO SAPIENS|0|TRANSFERASE","2KS1|Heterodimeric association of Transmembrane domains of ErbB1 and ErbB2 receptors Enabling Kinase Activation|SOLUTION NMR||Homo sapiens|0|TRANSFERASE","2M0B|Homodimeric transmembrane domain of the human receptor tyrosine kinase ErbB1 (EGFR, HER1) in micelles|SOLUTION NMR||Homo sapiens|0|MEMBRANE PROTEIN","2M20|EGFR transmembrane - juxtamembrane (TM-JM) segment in bicelles: MD guided NMR refined structure.|SOLUTION NMR||Homo sapiens|0|SIGNALING PROTEIN","2N5S|Spatial structure of EGFR transmembrane and juxtamembrane domains in DPC micelles|SOLUTION NMR||Homo sapiens|0|TRANSFERASE","2RF9|Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide|X-RAY DIFFRACTION|3.5|Homo sapiens|0|TRANSFERASE","2RFD|Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide|X-RAY DIFFRACTION|3.6|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSFERASE","2RFE|Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide|X-RAY DIFFRACTION|2.9|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSFERASE","2RGP|Structure of EGFR in complex with hydrazone, a potent dual inhibitor|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE","3B2U|Crystal structure of isolated domain III of the extracellular region of the epidermal growth factor receptor in complex with the Fab fragment of IMC-11F8|X-RAY DIFFRACTION|2.58|Homo sapiens|0|IMMUNE SYSTEM/TRANSFERASE","3B2V|Crystal structure of the extracellular region of the epidermal growth factor receptor in complex with the Fab fragment of IMC-11F8|X-RAY DIFFRACTION|3.3|Homo sapiens|0|IMMUNE SYSTEM/TRANSFERASE","3BEL|X-ray structure of EGFR in complex with oxime inhibitor|X-RAY DIFFRACTION|2.3|Homo sapiens|0|TRANSFERASE","3BUO|Crystal structure of c-Cbl-TKB domain complexed with its binding motif in EGF receptor'|X-RAY DIFFRACTION|2.6|Homo sapiens; SYNTHETIC CONSTRUCT|0|LIGASE/SIGNALING PROTEIN","3C09|Crystal structure the Fab fragment of matuzumab (Fab72000) in complex with domain III of the extracellular region of EGFR|X-RAY DIFFRACTION|3.2|Homo sapiens; Mus musculus|0|IMMUNE SYSTEM/TRANSFERASE","3G5V|Antibodies Specifically Targeting a Locally Misfolded Region of Tumor Associated EGFR|X-RAY DIFFRACTION|2.001|Mus musculus; SYNTHETIC CONSTRUCT|0|IMMUNE SYSTEM","3G5Y|Antibodies Specifically Targeting a Locally Misfolded Region of Tumor Associated EGFR|X-RAY DIFFRACTION|1.59|Mus musculus; SYNTHETIC CONSTRUCT|0|IMMUNE SYSTEM","3GOP|Crystal structure of the EGF receptor juxtamembrane and kinase domains|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE","3GT8|Crystal structure of the inactive EGFR kinase domain in complex with AMP-PNP|X-RAY DIFFRACTION|2.955|Homo sapiens|0|TRANSFERASE","3IKA|Crystal Structure of EGFR 696-1022 T790M Mutant Covalently Binding to WZ4002|X-RAY DIFFRACTION|2.9|Homo sapiens|0|TRANSFERASE","3LZB|EGFR kinase domain complexed with an imidazo[2,1-b]thiazole inhibitor|X-RAY DIFFRACTION|2.7|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3NJP|The Extracellular and Transmembrane Domain Interfaces in Epidermal Growth Factor Receptor Signaling|X-RAY DIFFRACTION|3.304|Homo sapiens|0|TRANSFERASE","3OB2|Crystal structure of c-Cbl TKB domain in complex with double phosphorylated EGFR peptide|X-RAY DIFFRACTION|2.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|Ligase/signaling Protein","3OP0|Crystal structure of Cbl-c (Cbl-3) TKB domain in complex with EGFR pY1069 peptide|X-RAY DIFFRACTION|2.52|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN/SIGNALING PROTEIN REGULATOR","3P0Y|anti-EGFR/HER3 Fab DL11 in complex with domain III of EGFR extracellular region|X-RAY DIFFRACTION|1.8|Homo sapiens|0|IMMUNE SYSTEM","3PFV|Crystal structure of Cbl-b TKB domain in complex with EGFR pY1069 peptide|X-RAY DIFFRACTION|2.27|Homo sapiens; SYNTHETIC CONSTRUCT|0|LIGASE/PROTEIN BINDING","3POZ|EGFR Kinase domain complexed with tak-285|X-RAY DIFFRACTION|1.5|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3QWQ|Crystal structure of the extracellular domain of the epidermal growth factor receptor in complex with an adnectin|X-RAY DIFFRACTION|2.75|Homo sapiens|0|PROTEIN BINDING/SIGNALING PROTEIN","3UG1|Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in the apo form|X-RAY DIFFRACTION|2.75|Homo sapiens|0|TRANSFERASE","3UG2|Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in complex with gefitinib|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3VJN|Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in complex with AMPPNP.|X-RAY DIFFRACTION|2.34|Homo sapiens|0|TRANSFERASE","3VJO|Crystal structure of the wild-type EGFR kinase domain in complex with AMPPNP.|X-RAY DIFFRACTION|2.64|Homo sapiens|0|TRANSFERASE","3VRP|Crystal structure of the tyrosine kinase binding domain of Cbl-c in complex with phospho-EGFR peptide|X-RAY DIFFRACTION|1.52|Homo sapiens; SYNTHETIC CONSTRUCT|0|PROTEIN BINDING/Transferase","3VRR|Crystal structure of the tyrosine kinase binding domain of Cbl-c (PL mutant) in complex with phospho-EGFR peptide|X-RAY DIFFRACTION|2|Homo sapiens; SYNTHETIC CONSTRUCT|0|PROTEIN BINDING/TRANSFERASE","3W2O|EGFR Kinase domain T790M/L858R Mutant with TAK-285|X-RAY DIFFRACTION|2.35|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3W2P|EGFR Kinase domain T790M/L858R mutant with compound 2|X-RAY DIFFRACTION|2.05|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3W2Q|EGFR kinase domain T790M/L858R mutant with HKI-272|X-RAY DIFFRACTION|2.2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3W2R|EGFR Kinase domain T790M/L858R mutant with compound 4|X-RAY DIFFRACTION|2.05|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3W2S|EGFR kinase domain with compound4|X-RAY DIFFRACTION|1.9|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3W32|EGFR kinase domain complexed with compound 20a|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3W33|EGFR kinase domain complexed with compound 19b|X-RAY DIFFRACTION|1.7|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4G5J|Crystal structure of EGFR kinase in complex with BIBW2992|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4G5P|Crystal structure of EGFR kinase T790M in complex with BIBW2992|X-RAY DIFFRACTION|3.17|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4HJO|Crystal structure of the inactive EGFR tyrosine kinase domain with erlotinib|X-RAY DIFFRACTION|2.75|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4I1Z|Crystal structure of the monomeric (V948R) form of the gefitinib/erlotinib resistant EGFR kinase domain L858R+T790M|X-RAY DIFFRACTION|3|Homo sapiens|0|TRANSFERASE","4I20|Crystal structure of monomeric (V948R) primary oncogenic mutant L858R EGFR kinase domain|X-RAY DIFFRACTION|3.34|Homo sapiens|0|TRANSFERASE","4I21|Crystal structure of L858R + T790M EGFR kinase domain in complex with MIG6 peptide|X-RAY DIFFRACTION|3.37|Homo sapiens|0|Transferase/Transferase Inhibitor","4I22|Structure of the monomeric (V948R)gefitinib/erlotinib resistant double mutant (L858R+T790M) EGFR kinase domain co-crystallized with gefitinib|X-RAY DIFFRACTION|1.71|Homo sapiens|0|TRANSFERASE","4I23|Crystal structure of the wild-type EGFR kinase domain in complex with dacomitinib (soaked)|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE","4I24|Structure of T790M EGFR kinase domain co-crystallized with dacomitinib|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE","4JQ7|Crystal structure of EGFR kinase domain in complex with compound 2a|X-RAY DIFFRACTION|2.73|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4JQ8|Crystal structure of EGFR kinase domain in complex with compound 4b|X-RAY DIFFRACTION|2.83|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4JR3|Crystal structure of EGFR kinase domain in complex with compound 3g|X-RAY DIFFRACTION|2.7|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4JRV|Crystal structure of EGFR kinase domain in complex with compound 4c|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4KRL|Nanobody/VHH domain 7D12 in complex with domain III of the extracellular region of EGFR, pH 6.0|X-RAY DIFFRACTION|2.849|Homo sapiens; Lama glama|0|TRANSFERASE/IMMUNE SYSTEM","4KRM|Nanobody/VHH domain 7D12 in complex with domain III of the extracellular region of EGFR, pH 3.5|X-RAY DIFFRACTION|2.655|Homo sapiens; Lama glama|0|TRANSFERASE/IMMUNE SYSTEM","4KRO|Nanobody/VHH domain EgA1 in complex with the extracellular region of EGFR|X-RAY DIFFRACTION|3.054|Homo sapiens; Lama glama; Mus musculus, Homo sapiens|0|TRANSFERASE/IMMUNE SYSTEM","4KRP|Nanobody/VHH domain 9G8 in complex with the extracellular region of EGFR|X-RAY DIFFRACTION|2.823|Homo sapiens; Lama glama; Mus musculus, Homo sapiens|0|TRANSFERASE/IMMUNE SYSTEM","4LI5|EGFR-K IN COMPLEX WITH N-[3-[[5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl]amino]-4-methoxy-phenyl] Prop-2-enamide|X-RAY DIFFRACTION|2.64|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4LL0|EGFR L858R/T790M in complex with PD168393|X-RAY DIFFRACTION|4|Homo sapiens|0|transferase/transferase inhibitor","4LQM|EGFR L858R in complex with PD168393|X-RAY DIFFRACTION|2.5|Homo sapiens|0|transferase/transferase inhibitor","4LRM|EGFR D770_N771insNPG in complex with PD168393|X-RAY DIFFRACTION|3.526|Homo sapiens|0|transferase/transferase inhibitor","4R3P|Crystal structures of EGFR in complex with Mig6|X-RAY DIFFRACTION|2.905|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSFERASE","4R3R|Crystal structures of EGFR in complex with Mig6|X-RAY DIFFRACTION|3.25|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSFERASE","4R5S|Crystal structure of EGFR 696-1022 L858R in complex with FIIN-3|X-RAY DIFFRACTION|3.001|Homo sapiens|0|TRANSFERASE","4RIW|Crystal structure of an EGFR/HER3 kinase domain heterodimer|X-RAY DIFFRACTION|3.1|Homo sapiens|0|TRANSFERASE","4RIX|Crystal structure of an EGFR/HER3 kinase domain heterodimer containing the cancer-associated HER3-Q790R mutation|X-RAY DIFFRACTION|3.1|Homo sapiens|0|TRANSFERASE","4RIY|Crystal structure of an EGFR/HER3 kinase domain heterodimer containing the cancer-associated HER3-E909G mutation|X-RAY DIFFRACTION|2.981|Homo sapiens|0|TRANSFERASE","4RJ4|EGFR kinase (T790M/L858R) with inhibitor compound 6|X-RAY DIFFRACTION|2.78|Homo sapiens|0|Transferase/transferase inhibitor","4RJ5|EGFR kinase (T790M/L858R) with inhibitor compound 5|X-RAY DIFFRACTION|3.1|Homo sapiens|0|Transferase/Transferase inhibitor","4RJ6|EGFR kinase (T790M/L858R) with inhibitor compound 4|X-RAY DIFFRACTION|2.7|Homo sapiens|0|Transferase/Transferase inhibitor","4RJ7|EGFR kinase (T790M/L858R) with inhibitor compound 1|X-RAY DIFFRACTION|2.55|Homo sapiens|0|Transferase/Transferase inhibitor"]}]}