| 2GS7 |
2.6 |
Crystal Structure of the inactive EGFR kinase domain in complex with AMP-PNP |
| 2EB3 |
2.84 |
Crystal structure of mutated EGFR kinase domain (L858R) in complex with AMPPNP |
| 6B3S |
2.8 |
Crystal structure of the Fab fragment of necitumumab (Fab11F8) in complex with domain III from a cetuximab resistant variant of EGFR (sEGFRd3-S468R) |
| 5HCY |
2.46 |
EGFR kinase domain mutant TMLR with 3-carboxamide azaindole compound 13 |
| 3QWQ |
2.75 |
Crystal structure of the extracellular domain of the epidermal growth factor receptor in complex with an adnectin |
| 8A2D |
1.11 |
EGFR kinase domain (L858R/V948R) in complex with 2-[4-(difluoromethyl)-6-[2-[4-[[4-(hydroxymethyl)-1-piperidyl]methyl]phenyl]ethynyl]-7-methyl-indazol-2-yl]-2-spiro[6,7-dihydropyrrolo[1,2-c]imidazole-5,1'-cyclopropane]-1-yl-N-thiazol-2-yl-acetamide |
| 3W2P |
2.05 |
EGFR Kinase domain T790M/L858R mutant with compound 2 |
| 5GTZ |
2.999 |
Crystal structure of EGFR 696-1022 T790M in complex with JTS-1-39 |
| 7SZ0 |
3.3 |
Cryo-EM structure of the extracellular module of the full-length EGFR L834R bound to EGF. tips-juxtaposed conformation |
| 7KY0 |
3.1 |
Inactive conformation of EGFR (T790M/V948R) kinase in complex with BI-4020 |
| 5SX4 |
2.8 |
Crystal Structure of panitumumab in complex with epidermal growth factor receptor domain 3. |
| 4TKS |
3.2017 |
Native-SAD phasing for human EGFR kinase domain. |
| 7SZ7 |
3.4 |
Cryo-EM structure of the extracellular module of the full-length EGFR bound to TGF-alpha. tips-juxtaposed conformation |
| 3GT8 |
2.955 |
Crystal structure of the inactive EGFR kinase domain in complex with AMP-PNP |
| 2ITT |
2.73 |
Crystal structure of EGFR kinase domain L858R mutation in complex with AEE788 |
| 6TFU |
2.0 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 14d |
| 7T4J |
2.2 |
Crystal Structure of EGFR_D770_N771insNPG/V948R in complex with TAK-788 |
| 6LUB |
2.315 |
Crystal Structure of EGFR(L858R/T790M/C797S) in complex with CH7233163 |
| 3G5V |
2.001 |
Antibodies Specifically Targeting a Locally Misfolded Region of Tumor Associated EGFR |
| 5CAV |
2.73 |
EGFR kinase domain with compound 41a |
| 7JXL |
2.4 |
EGFR kinase (T790M/V948R) in complex with AZ5104 |
| 4RJ8 |
2.5 |
EGFR kinase (T790M/L858R) with inhibitor compound 8 |
| 3LZB |
2.7 |
EGFR kinase domain complexed with an imidazo[2,1-b]thiazole inhibitor |
| 1IVO |
3.3 |
Crystal Structure of the Complex of Human Epidermal Growth Factor and Receptor Extracellular Domains. |
| 7SYE |
3.3 |
Cryo-EM structure of the extracellular module of the full-length EGFR bound to EGF. tips-separated conformation |
| 6S8A |
2.6 |
Crystal Structure of EGFR-T790M/C797S in Complex with Covalent Pyrrolopyrimidine 19h |
| 3VRP |
1.52 |
Crystal structure of the tyrosine kinase binding domain of Cbl-c in complex with phospho-EGFR peptide |
| 4I20 |
3.34 |
Crystal structure of monomeric (V948R) primary oncogenic mutant L858R EGFR kinase domain |
| 7VRE |
2.507 |
The crystal structure of EGFR T790M/C797S with the inhibitor HCD2892 |
| 2ITV |
2.47 |
Crystal structure of EGFR kinase domain L858R mutation in complex with AMP-PNP |
| 3P0Y |
1.8 |
anti-EGFR/HER3 Fab DL11 in complex with domain III of EGFR extracellular region |
| 6S9D |
2.67 |
EGFR-KINASE IN COMPLEX WITH COMPOUND 6 |
| 5CNO |
1.55 |
Crystal structure of the EGFR kinase domain mutant V924R |
| 5HIC |
2.6 |
EGFR kinase domain mutant TMLR with a imidazopyridinyl-aminopyrimidine inhibitor |
| 4WKQ |
1.85 |
1.85 angstrom structure of EGFR kinase domain with gefitinib |
| 3GOP |
2.8 |
Crystal structure of the EGF receptor juxtamembrane and kinase domains |
| 8A2A |
1.43 |
EGFR kinase domain in complex with 2-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-1-yl)-2-[6-[2-[4-[[4-(hydroxymethyl)-1-piperidyl]methyl]phenyl]ethynyl]-1-oxo-4-(trifluoromethyl)isoindolin-2-yl]-N-thiazol-2-yl-acetamide (form 2) |
| 7JXQ |
1.83 |
EGFR kinase (T790M/V948R) in complex with allosteric inhibitor JBJ-09-063 |
| 7LFR |
3.2 |
Crystal structure of the epidermal growth factor receptor extracellular region with R84K mutation in complex with epiregulin crystallized with spermine |
| 4JR3 |
2.7 |
Crystal structure of EGFR kinase domain in complex with compound 3g |
| 3W2O |
2.35 |
EGFR Kinase domain T790M/L858R Mutant with TAK-285 |
| 7TVD |
2.96 |
Crystal structure of the kinase domain of EGFR exon-19 (del-747-749) mutant |
| 6Z4D |
2.0 |
Crystal Structure of EGFR-T790M/V948R in Complex with Mavelertinib and EAI001 |
| 6TG0 |
1.5 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 21a |
| 5X2A |
1.85 |
Crystal structure of EGFR 696-1022 T790M/V948R in complex with SKLB(3) |
| 5Y25 |
3.102 |
EGFR kinase domain mutant (T790M/L858R) with covalent ligand NS-062 |
| 7SZ5 |
3.6 |
Cryo-EM structure of the extracellular module of the full-length EGFR bound to TGF-alpha tips-separated conformation |
| 7SZ1 |
3.4 |
Cryo-EM structure of the extracellular module of the full-length EGFR L834R bound to EGF. tips-separated conformation |
| 5X2F |
2.2 |
Crystal structure of EGFR 696-1022 T790M/V948R in complex with SKLB(6) |
| 3OB2 |
2.1 |
Crystal structure of c-Cbl TKB domain in complex with double phosphorylated EGFR peptide |
| 6LUD |
2.05 |
Crystal Structure of EGFR(L858R/T790M/C797S) in complex with Osimertinib |
| 5XWD |
2.894 |
Crystal structure of the complex of 059-152-Fv and EGFR-ECD |
| 5X28 |
2.952 |
Crystal structure of EGFR 696-1022 L858R in complex with SKLB(6) |
| 3VJO |
2.64 |
Crystal structure of the wild-type EGFR kinase domain in complex with AMPPNP. |
| 3UG1 |
2.75 |
Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in the apo form |
| 7U98 |
3.42 |
EGFR(T790M/V948R) in complex with a macrocyclic inhibitor |
| 6JX4 |
2.531 |
Crystal structure of EGFR 696-1022 T790M in complex with AZD9291 prepared by soaking |
| 3NJP |
3.304 |
The Extracellular and Transmembrane Domain Interfaces in Epidermal Growth Factor Receptor Signaling |
| 4ZAU |
2.8 |
AZD9291 complex with wild type EGFR |
| 6V66 |
1.79 |
EGFR(T790M/V948R) in complex with LN2899 |
| 5CZI |
2.6 |
EGFR L858R MUTANT IN COMPLEX WITH A SHC PEPTIDE SUBSTRATE |
| 6V6K |
2.2 |
EGFR(T790M/V948R) in complex with LN2057 |
| 7JXK |
3.1 |
EGFR kinase (T790M/V948R) in complex with PF-06747775 and JBJ-04-125-02 |
| 2JIT |
3.1 |
Crystal structure of EGFR kinase domain T790M mutation |
| 3W33 |
1.7 |
EGFR kinase domain complexed with compound 19b |
| 4WRG |
1.9 |
1.9 angstrom structure of EGFR kinase domain |
| 7JXW |
2.5 |
EGFR kinase (T790M/V948R) in complex with osimertinib and JBJ-09-063 |
| 7LFS |
3.5 |
Crystal structure of the epidermal growth factor receptor extracellular region with A265V mutation in complex with epiregulin |
| 5HG8 |
1.42 |
EGFR (L858R, T790M, V948R) in complex with N-[3-({2-[(1-methyl-1H-pyrazol-4-yl)amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}oxy)phenyl]prop-2-enamide |
| 4RJ6 |
2.7 |
EGFR kinase (T790M/L858R) with inhibitor compound 4 |
| 6V5N |
2.4 |
EGFR(T790M/V948R) in complex with LN2084 |
| 4RJ5 |
3.1 |
EGFR kinase (T790M/L858R) with inhibitor compound 5 |
| 7U99 |
2.5 |
EGFR kinase in complex with a macrocyclic inhibitor |
| 6JWL |
2.551 |
Crystal structure of EGFR 696-1022 L858R in complex with AZD9291 |
| 5XGM |
2.952 |
Crystal structure of EGFR 696-1022 T790M in complex with Go6976 |
| 4RJ4 |
2.78 |
EGFR kinase (T790M/L858R) with inhibitor compound 6 |
| 5EDR |
2.6 |
EGFR kinase (T790M/L858R) with inhibitor compound 27: ~{N}-(1~{H}-indazol-3-yl)-7,7-dimethyl-2-(2-methylpyrazol-3-yl)-5~{H}-furo[3,4-d]pyrimidin-4-amine |
| 5CAS |
2.1 |
EGFR kinase domain mutant TMLR with compound 41a |
| 4LRM |
3.526 |
EGFR D770_N771insNPG in complex with PD168393 |
| 6V5P |
2.3 |
EGFR(T790M/V948R) in complex with LN2725 |
| 6TG1 |
1.6 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 21b |
| 7K1H |
2.602 |
EGFR L858R/V948R in complex with osimertinib and allosteric inhibitor JBJ-09-063 |
| 4KRM |
2.655 |
Nanobody/VHH domain 7D12 in complex with domain III of the extracellular region of EGFR, pH 3.5 |
| 3UG2 |
2.5 |
Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in complex with gefitinib |
| 6S9C |
2.73 |
EGFR-KINASE IN COMPLEX WITH COMPOUND 5 |
| 5SX5 |
2.5 |
Crystal Structure of panitumumab in complex with epidermal growth factor receptor domain 3 mutant S468R. |
| 4I21 |
3.37 |
Crystal structure of L858R + T790M EGFR kinase domain in complex with MIG6 peptide |
| 3BEL |
2.3 |
X-ray structure of EGFR in complex with oxime inhibitor |
| 7ER2 |
2.662 |
Crystal structure of EGFR 696-1022 T790M/C797S in complex with LS_2_40 |
| 5CZH |
2.8 |
EGFR L858R MUTANT IN COMPLEX WITH AN OPTIMAL PEPTIDE SUBSTRATE |
| 5HG7 |
1.85 |
EGFR (L858R, T790M, V948R) in complex with 1-{(3R,4R)-3-[5-Chloro-2-(1-methyl-1H-pyrazol-4-ylamino)-7H-pyrrolo[2,3-d]pyrimidin-4-yloxymethyl]-4-methoxy-pyrrolidin-1-yl}propenone (PF-06459988) |
| 7A6K |
2.0 |
Crystal Structure of EGFR-T790M/V948R in Complex with TAK-788 |
| 5CAL |
2.7 |
EGFR kinase domain mutant TMLR with compound 24 |
| 8HGO |
3.31 |
The EGF-bound EGFR/HER2 ectodomain complex |
| 5EDQ |
2.8 |
EGFR kinase (T790M/L858R) with inhibitor compound 15: ~{N}-(7-chloranyl-1~{H}-indazol-3-yl)-7,7-dimethyl-2-(1~{H}-pyrazol-4-yl)-5~{H}-furo[3,4-d]pyrimidin-4-amine |
| 3C09 |
3.2 |
Crystal structure the Fab fragment of matuzumab (Fab72000) in complex with domain III of the extracellular region of EGFR |
| 7SI1 |
1.6 |
Crystal structure of apo EGFR kinase domain |
| 4R5S |
3.001 |
Crystal structure of EGFR 696-1022 L858R in complex with FIIN-3 |
| 7LEN |
2.9 |
Crystal structure of the epidermal growth factor receptor extracellular region with R84K mutation in complex with epiregulin crystallized with trehalose |
| 6WAK |
2.4 |
A crystal structure of EGFR(T790M/V948R) in complex with LN3754 |
| 5FEE |
2.7 |
EGFR kinase domain T790M mutant in complex with a covalent aminobenzimidazole inhibitor. |
| 7OM4 |
6.05 |
Nanobody EgB4 bound to the full extracellular EGFR-EGF complex |
| 5YU9 |
1.95 |
Crystal structure of EGFR 696-1022 T790M in complex with Ibrutinib |
| 6WXN |
1.76 |
EGFR(T790M/V948R) in complex with LN3844 |
| 6JXT |
2.307 |
Crystal structure of EGFR 696-1022 WT in complex with AZD9291 prepared by cocrystallization |
| 5EM7 |
2.81 |
EGFR kinase domain mutant TMLR with pyridone compound 13: 4-[(2-methoxyphenyl)amino]-~{N}-[4-(4-methylpiperazin-1-yl)phenyl]-2-oxidanylidene-1~{H}-pyridine-3-carboxamide |
| 4JQ7 |
2.73 |
Crystal structure of EGFR kinase domain in complex with compound 2a |
| 3VJN |
2.34 |
Crystal structure of the mutated EGFR kinase domain (G719S/T790M) in complex with AMPPNP. |
| 1XKK |
2.4 |
EGFR kinase domain complexed with a quinazoline inhibitor- GW572016 |
| 6TFV |
1.5 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 18b |
| 5WB7 |
2.941 |
Crystal structure of the epidermal growth factor receptor extracellular region in complex with epiregulin |
| 8A2B |
1.69 |
EGFR kinase domain (L858R/V948R) in complex with 2-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-1-yl)-2-[6-[2-[4-[[4-(hydroxymethyl)-1-piperidyl]methyl]phenyl]ethynyl]-1-oxo-4-(trifluoromethyl)isoindolin-2-yl]-N-thiazol-2-yl-acetamide |
| 5HG5 |
1.52 |
EGFR (L858R, T790M, V948R) in complex with N-{3-[(2-{[4-(4-methylpiperazin-1-yl)phenyl]amino}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy]phenyl}prop-2-enamide |
| 6JRX |
2.201 |
EGFR T790M/C797S in complex with compound 6i |
| 2EB2 |
2.5 |
Crystal structure of mutated EGFR kinase domain (G719S) |
| 5HCX |
2.6 |
EGFR kinase domain mutant TMLR with azabenzimidazole compound 7 |
| 1Z9I |
|
A Structural Model for the Membrane-Bound Form of the Juxtamembrane Domain of the Epidermal Growth Factor Receptor |
| 7LGS |
3.1 |
Structure of EGFR_D770_N771insNPG/V948R in complex with covalent inhibitor Osimertinib. |
| 5Y9T |
3.25 |
Crystal Structure of EGFR T790M mutant in complex with naquotinib |
| 5CAQ |
2.5 |
EGFR kinase domain mutant TMLR with compound 33 |
| 5XGN |
3.0 |
Crystal structure of EGFR 696-1022 T790M/C797S in complex with Go6976 |
| 5X2C |
2.05 |
Crystal structure of EGFR 696-1022 T790M/V948R in complex with SKLB(5) |
| 4HJO |
2.75 |
Crystal structure of the inactive EGFR tyrosine kinase domain with erlotinib |
| 5EM6 |
2.78 |
EGFR kinase domain mutant TMLR with pyridone compound 19: 4-[(2-azanylpyrimidin-4-yl)amino]-~{N}-[4-(4-methylpiperazin-1-yl)phenyl]-2-oxidanylidene-1~{H}-pyridine-3-carboxamide |
| 5X26 |
2.951 |
Crystal structure of EGFR 696-1022 L858R in complex with SKLB(3) |
| 2ITP |
2.74 |
Crystal structure of EGFR kinase domain G719S mutation in complex with AEE788 |
| 2ITY |
3.42 |
Crystal structure of EGFR kinase domain in complex with Iressa |
| 5UGC |
1.58 |
Crystal structure of the EGFR kinase domain (L858R, T790M, V948R) in complex with a covalent inhibitor N-[(3R,4R)-4-fluoro-1-{6-[(3-methoxy-1-methyl-1H-pyrazol-4-yl)amino]-9-methyl-9H-purin-2-yl}pyrrolidin-3-yl]propanamide |
| 7UKW |
2.6 |
EGFR(T790M/V948R) in complex with Lazertinib (YH25448) |
| 3W2Q |
2.2 |
EGFR kinase domain T790M/L858R mutant with HKI-272 |
| 2ITQ |
2.68 |
Crystal structure of EGFR kinase domain G719S mutation in complex with AFN941 |
| 7T4I |
2.61 |
Crystal Structure of wild type EGFR in complex with TAK-788 |
| 8D76 |
2.4 |
Crystal Structure of EGFR LRTM with compound 24 |
| 6JX0 |
2.53 |
Crystal structure of EGFR 696-1022 T790M in complex with AZD9291 prepared by co-crystallization |
| 7K1I |
3.202 |
EGFR kinase (L858R/V948R) in complex with allosteric inhibitor JBJ-09-063 |
| 7U9A |
2.6 |
EGFR in complex with a macrocyclic inhibitor |
| 2GS6 |
2.6 |
Crystal Structure of the active EGFR kinase domain in complex with an ATP analog-peptide conjugate |
| 5C8N |
2.401 |
EGFR kinase domain mutant TMLR with compound 23 |
| 8A27 |
1.07 |
EGFR kinase domain in complex with 2-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-1-yl)-2-[6-[2-[4-[[4-(hydroxymethyl)-1-piperidyl]methyl]phenyl]ethynyl]-1-oxo-4-(trifluoromethyl)isoindolin-2-yl]-N-thiazol-2-yl-acetamide |
| 6WA2 |
2.4 |
Crystal structure of EGFR(T790M/V948R) in complex with LN3753 |
| 3POZ |
1.5 |
EGFR Kinase domain complexed with tak-285 |
| 7JXM |
2.192 |
EGFR kinase (T790M/V948R) in complex with osimertinib and EAI045 |
| 5GTY |
3.14 |
Crystal structure of EGFR 696-1022 T790M in complex with LXX-6-26 |
| 5UWD |
3.06 |
Crystal structure of EGFR kinase domain (L858R, T790M, V948R) in complex with the covalent inhibitor CO-1686 |
| 5JEB |
3.298 |
Crystal structure of EGFR tyrosine kinase domain with novel inhibitor of active state of HER2 |
| 2RGP |
2.0 |
Structure of EGFR in complex with hydrazone, a potent dual inhibitor |
| 6XL4 |
2.06 |
EGFR(T790M/V948R) in complex with AZD9291 and DDC4002 |
| 5CNN |
1.9 |
Crystal structure of the EGFR kinase domain mutant I682Q |
| 1MOX |
2.5 |
Crystal Structure of Human Epidermal Growth Factor Receptor (residues 1-501) in complex with TGF-alpha |
| 4G5P |
3.17 |
Crystal structure of EGFR kinase T790M in complex with BIBW2992 |
| 4ZJV |
2.7 |
crystal structure of EGFR kinase domain in complex with Mitogen-inducible gene 6 protein |
| 4RJ7 |
2.55 |
EGFR kinase (T790M/L858R) with inhibitor compound 1 |
| 7A6J |
2.0 |
Crystal Structure of EGFR-T790M/V948R in Complex with Poziotinib |
| 2RF9 |
3.5 |
Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide |
| 4JQ8 |
2.83 |
Crystal structure of EGFR kinase domain in complex with compound 4b |
| 2J5E |
3.1 |
Crystal structure of EGFR kinase domain in complex with an irreversible inhibitor 13-jab |
| 5WB8 |
3.0 |
Crystal structure of the epidermal growth factor receptor extracellular region in complex with epigen |
| 5HIB |
2.85 |
EGFR kinase domain mutant TMLR with a pyrazolopyrimidine inhibitor |
| 5CAU |
2.25 |
EGFR kinase domain mutant TMLR with compound 41b |
| 5UG8 |
1.46 |
Crystal structure of the EGFR kinase domain (L858R, T790M, V948R) in complex with a covalent inhibitor N-[(3R,4R)-4-fluoro-1-{6-[(1-methyl-1H-pyrazol-4-yl)amino]-9-(propan-2-yl)-9H-purin-2-yl}pyrrolidin-3-yl]propanamide |
| 4RIY |
2.981 |
Crystal structure of an EGFR/HER3 kinase domain heterodimer containing the cancer-associated HER3-E909G mutation |
| 6S89 |
2.701 |
Crystal Structure of EGFR-T790M/C797S in Complex with Covalent Pyrrolopyrimidine 19g |
| 2ITU |
2.8 |
Crystal structure of EGFR kinase domain L858R mutation in complex with AFN941 |
| 5C8M |
2.9 |
EGFR kinase domain mutant TMLR with compound 17 |
| 4I1Z |
3.0 |
Crystal structure of the monomeric (V948R) form of the gefitinib/erlotinib resistant EGFR kinase domain L858R+T790M |
| 7VRA |
2.41 |
The crystal structure of EGFR T790M/C797S with the inhibitor HC5476 |
| 2GS2 |
2.8 |
Crystal Structure of the active EGFR kinase domain |
| 6DUK |
2.2 |
EGFR with an allosteric inhibitor |
| 6VHN |
2.4 |
Wild type EGFR in complex with LN2057 |
| 3W32 |
1.8 |
EGFR kinase domain complexed with compound 20a |
| 2ITO |
3.25 |
Crystal structure of EGFR kinase domain G719S mutation in complex with Iressa |
| 6V6O |
2.1 |
EGFR(T790M/V948R) in complex with LN2380 |
| 4LI5 |
2.64 |
EGFR-K IN COMPLEX WITH N-[3-[[5-chloro-4-(1H-indol-3-yl)pyrimidin-2-yl]amino]-4-methoxy-phenyl] Prop-2-enamide |
| 6TFY |
1.7 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 18c |
| 5HCZ |
2.62 |
EGFR kinase domain mutant TMLR with 3-azetidinyl azaindazole compound 21 |
| 6JRJ |
2.943 |
The structure of co-crystals of 8r-B-EGFR T790M/C797S complex |
| 6TFW |
2.0 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 18d |
| 2ITW |
2.88 |
Crystal structure of EGFR kinase domain in complex with AFN941 |
| 5XDL |
2.7 |
Crystal structure of EGFR 696-1022 L858R in complex with CO-1686 |
| 1M14 |
2.6 |
Tyrosine Kinase Domain from Epidermal Growth Factor Receptor |
| 4UV7 |
2.1 |
The complex structure of extracellular domain of EGFR and GC1118A |
| 3BUO |
2.6 |
Crystal structure of c-Cbl-TKB domain complexed with its binding motif in EGF receptor' |
| 1NQL |
2.8 |
Structure of the extracellular domain of human epidermal growth factor (EGF) receptor in an inactive (low pH) complex with EGF. |
| 6S9B |
3.25 |
EGFR-KINASE IN COMPLEX WITH COMPOUND 1 |
| 7A6I |
2.4 |
Crystal Structure of EGFR-T790M/V948R in Complex with LDC8201 |
| 2RFE |
2.9 |
Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide |
| 2ITX |
2.98 |
Crystal structure of EGFR kinase domain in complex with AMP-PNP |
| 6P8Q |
1.9 |
EGFR in complex with a dihydrodibenzodiazepinone allosteric inhibitor. |
| 5J9Y |
2.8 |
EGFR-T790M in complex with pyrazolopyrimidine inhibitor 1b |
| 3VRR |
2.0 |
Crystal structure of the tyrosine kinase binding domain of Cbl-c (PL mutant) in complex with phospho-EGFR peptide |
| 5UGB |
2.53 |
Crystal structure of the EGFR kinase domain in complex with 4-(4-{[2-{[(3S)-1-acetylpyrrolidin-3-yl]amino}-9-(propan-2-yl)-9H-purin-6-yl]amino}phenyl)-1-methylpiperazin-1-ium |
| 5UG9 |
1.33 |
Crystal structure of the EGFR kinase domain (L858R, T790M, V948R) in complex with a covalent inhibitor N-[(3R,4R)-4-fluoro-1-{6-[(3-methoxy-1-methyl-1H-pyrazol-4-yl)amino]-9-(propan-2-yl)-9H-purin-2-yl}pyrrolidin-3-yl]propanamide |
| 5UGA |
1.82 |
Crystal structure of the EGFR kinase domain (L858R, T790M, V948R) in complex with 4-(4-{[2-{[(3S)-1-acetylpyrrolidin-3-yl]amino}-9-(propan-2-yl)-9H-purin-6-yl]amino}phenyl)-1-methylpiperazin-1-ium |
| 5X2K |
3.201 |
Crystal structure of EGFR 696-1022 T790M in complex with WZ4003 |
| 5CAN |
2.8 |
EGFR kinase domain mutant TMLR with compound 27 |
| 4ZSE |
1.97 |
Crystal structure of EGFR 696-1022 T790M/V948R, crystal form II |
| 4RIX |
3.1 |
Crystal structure of an EGFR/HER3 kinase domain heterodimer containing the cancer-associated HER3-Q790R mutation |
| 7OXB |
2.56 |
Crystal structure of EGFR double mutant (T790M/L858R) in complex with compound 6. |
| 7LTX |
2.3 |
EGFR (T790M/V948R) in complex with quinazolinone allosteric inhibitor |
| 5LV6 |
|
N-terminal motif dimerization of EGFR transmembrane domain in bicellar environment |
| 5CAO |
2.6 |
EGFR kinase domain mutant TMLR with compound 29 |
| 2ITN |
2.47 |
Crystal structure of EGFR kinase domain G719S mutation in complex with AMP-PNP |
| 6P1D |
2.4 |
Crystal structure of EGFR with mutant-selective dihydrodibenzodiazepinone allosteric inhibitor |
| 5ZWJ |
2.9 |
Crystal structure of EGFR 675-1022 T790M/C797S/V948R in complex with EAI045 |
| 2RFD |
3.6 |
Crystal structure of the complex between the EGFR kinase domain and a Mig6 peptide |
| 6D8E |
2.537 |
Discovery of a Highly Potent and Broadly Effective EGFR and HER2 Exon 20 Insertion Mutant Inhibitor |
| 4I24 |
1.8 |
Structure of T790M EGFR kinase domain co-crystallized with dacomitinib |
| 5ZTO |
2.649 |
Crystal structure of EGFR 696-1022 T790M/C797S in complex with D3003 |
| 7LG8 |
2.93 |
EGFR (T79M/V948R) in complex with naquotinib and an allosteric inhibitor |
| 5CAP |
2.4 |
EGFR kinase domain mutant TMLR with compound 30 |
| 3G5Y |
1.59 |
Antibodies Specifically Targeting a Locally Misfolded Region of Tumor Associated EGFR |
| 2ITZ |
2.8 |
Crystal structure of EGFR kinase domain L858R mutation in complex with Iressa |
| 5GMP |
2.797 |
Crystal structure of EGFR 696-1022 T790M in complex with XTF-262 |
| 4LL0 |
4.0 |
EGFR L858R/T790M in complex with PD168393 |
| 3B2U |
2.58 |
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 |
| 6VHP |
3.6 |
Wild type EGFR in complex with LN2899 |
| 7SYD |
3.1 |
Cryo-EM structure of the extracellular module of the full-length EGFR bound to EGF tips-juxtaposed conformation |
| 7B85 |
2.5 |
Crystal Structure of EGFR-WT in Complex with TAK-788 |
| 6P1L |
2.8 |
Crystal structure of EGFR in complex with EAI045 |
| 2JIV |
3.5 |
Crystal structure of EGFR kinase domain T790M mutation in compex with HKI-272 |
| 4R3P |
2.905 |
Crystal structures of EGFR in complex with Mig6 |
| 7JXP |
2.16 |
EGFR kinase (T790M/V948R) in complex with osimertinib and JBJ-04-125-02 |
| 5GNK |
1.796 |
Crystal structure of EGFR 696-988 T790M in complex with LXX-6-34 |
| 6TFZ |
1.8 |
Crystal Structure of EGFR T790M/V948R in Complex with Covalent Pyrrolopyrimidine 19 |
| 5EM8 |
2.8 |
EGFR kinase domain with pyridone compound 13: 4-[(2-methoxyphenyl)amino]-~{N}-[4-(4-methylpiperazin-1-yl)phenyl]-2-oxidanylidene-1~{H}-pyridine-3-carboxamide |
| 7AEI |
2.65 |
Studies Towards a Reversible EGFR C797S Triple Mutant Inhibitor Series |
| 2M20 |
|
EGFR transmembrane - juxtamembrane (TM-JM) segment in bicelles: MD guided NMR refined structure. |
| 4I22 |
1.71 |
Structure of the monomeric (V948R)gefitinib/erlotinib resistant double mutant (L858R+T790M) EGFR kinase domain co-crystallized with gefitinib |
| 5U8L |
1.6 |
Crystal structure of EGFR kinase domain in complex with a sulfonyl fluoride probe XO44 |
| 4WD5 |
3.3 |
Crystal structure of EGFR 696-1022 T790M in complex with QL-X138 |
| 4KRO |
3.054 |
Nanobody/VHH domain EgA1 in complex with the extracellular region of EGFR |
| 3W2S |
1.9 |
EGFR kinase domain with compound4 |
| 7UKV |
2.4 |
Wild type EGFR in complex with Lazertinib (YH25448) |
| 2J5F |
3.0 |
Crystal structure of EGFR kinase domain in complex with an irreversible inhibitor 34-jab |
| 1YY9 |
2.605 |
Structure of the extracellular domain of the epidermal growth factor receptor in complex with the Fab fragment of cetuximab/Erbitux/IMC-C225 |
| 6JRK |
2.796 |
The structure of co-crystals of 8r-B-EGFR WT complex |
| 4UIP |
2.95 |
The complex structure of extracellular domain of EGFR with Repebody (rAC1). |
| 4RIW |
3.1 |
Crystal structure of an EGFR/HER3 kinase domain heterodimer |
| 2M0B |
|
Homodimeric transmembrane domain of the human receptor tyrosine kinase ErbB1 (EGFR, HER1) in micelles |
| 5X27 |
2.952 |
Crystal structure of EGFR 696-1022 L858R in complex with SKLB(5) |
| 3W2R |
2.05 |
EGFR Kinase domain T790M/L858R mutant with compound 4 |
| 4KRL |
2.849 |
Nanobody/VHH domain 7D12 in complex with domain III of the extracellular region of EGFR, pH 6.0 |
| 8D73 |
2.17 |
Crystal Structure of EGFR LRTM with compound 7 |
| 5HG9 |
2.15 |
EGFR (L858R, T790M, V948R) in complex with 1-[(3R,4R)-3-[({2-[(1-methyl-1H-pyrazol-4-yl)amino]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}oxy)methyl]-4-(trifluoromethyl)pyrrolidin-1-yl]prop-2-en-1-one |
| 2J6M |
3.1 |
Crystal structure of EGFR kinase domain in complex with AEE788 |
| 7AEM |
2.65 |
Studies Towards a Reversible EGFR C797S Triple Mutant Inhibitor Series |
| 8HGS |
3.81 |
The EGF-bound EGFR ectodomain homodimer |
| 5C8K |
3.0 |
EGFR kinase domain mutant TMLR with compound 1 |
| 7KXZ |
2.4 |
Active conformation of EGFR kinase in complex with BI-4020 |
| 7JXI |
3.0 |
EGFR kinase (T790M/V948R) in complex with PF-06747775 |
| 5FEQ |
3.4 |
EGFR KINASE DOMAIN IN COMPLEX WITH A COVALENT AMINOBENZIMIDAZOLE |
| 8HGP |
4.53 |
The EREG-bound EGFR/HER2 ectodomain complex |
| 4G5J |
2.8 |
Crystal structure of EGFR kinase in complex with BIBW2992 |
| 2N5S |
|
Spatial structure of EGFR transmembrane and juxtamembrane domains in DPC micelles |
| 5J9Z |
2.5 |
EGFR-T790M in complex with pyrazolopyrimidine inhibitor 1a |
| 4KRP |
2.823 |
Nanobody/VHH domain 9G8 in complex with the extracellular region of EGFR |
| 3IKA |
2.9 |
Crystal Structure of EGFR 696-1022 T790M Mutant Covalently Binding to WZ4002 |
| 3B2V |
3.3 |
Crystal structure of the extracellular region of the epidermal growth factor receptor in complex with the Fab fragment of IMC-11F8 |
| 1M17 |
2.6 |
Epidermal Growth Factor Receptor tyrosine kinase domain with 4-anilinoquinazoline inhibitor erlotinib |
| 6JZ0 |
2.86 |
Crystal structure of EGFR kinase domain in complex with compound 78 |
| 5EDP |
2.9 |
EGFR kinase (T790M/L858R) apo |
| 3PFV |
2.27 |
Crystal structure of Cbl-b TKB domain in complex with EGFR pY1069 peptide |
| 2JIU |
3.05 |
Crystal structure of EGFR kinase domain T790M mutation in complex with AEE788 |
| 5FED |
2.651 |
EGFR kinase domain in complex with a covalent aminobenzimidazole inhibitor. |
| 5EM5 |
2.65 |
EGFR kinase domain mutant TMLR with pyridone compound 2: 4-[2-(4-chlorophenyl)ethylamino]-~{N}-[4-(4-methylpiperazin-1-yl)phenyl]-2-oxidanylidene-1~{H}-pyridine-3-carboxamide |
| 6Z4B |
2.5 |
Crystal Structure of EGFR-T790M/V948R in Complex with Osimertinib and EAI045 |
| 5XDK |
2.346 |
Crystal structure of EGFR 696-1022 T790M in complex with CO-1686 |
| 3OP0 |
2.52 |
Crystal structure of Cbl-c (Cbl-3) TKB domain in complex with EGFR pY1069 peptide |
| 5D41 |
2.31 |
EGFR kinase domain in complex with mutant selective allosteric inhibitor |
| 4LQM |
2.5 |
EGFR L858R in complex with PD168393 |
| 2KS1 |
|
Heterodimeric association of Transmembrane domains of ErbB1 and ErbB2 receptors Enabling Kinase Activation |
| 6ARU |
3.2 |
Structure of Cetuximab Fab mutant in complex with EGFR extracellular domain |
| 7A2A |
1.9 |
Crystal Structure of EGFR-T790M/V948R in Complex with Spebrutinib and EAI001 |
| 4JRV |
2.8 |
Crystal structure of EGFR kinase domain in complex with compound 4c |
| 4I23 |
2.8 |
Crystal structure of the wild-type EGFR kinase domain in complex with dacomitinib (soaked) |
| 6VH4 |
2.8 |
Wild type EGFR in complex with LN2380 |
| 4R3R |
3.25 |
Crystal structures of EGFR in complex with Mig6 |