Structural Analysis of the Mechanism of Inhibition and Allosteric Activation of the Kinase Domain of HER2 Protein
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Photo-activated psoralen binds the ErbB2 catalytic kinase domain, blocking ErbB2 signaling and triggering tumor cell apoptosisHER2 driven non-small cell lung cancer (NSCLC): potential therapeutic approachesQuantification of HER family receptors in breast cancerDesign, biological evaluation and 3D QSAR studies of novel dioxin-containing pyrazoline derivatives with thiourea skeleton as selective HER-2 inhibitors.A single ligand is sufficient to activate EGFR dimersActivating HER2 mutations in HER2 gene amplification negative breast cancerCollaborative enhancement of antibody binding to distinct PECAM-1 epitopes modulates endothelial targetingContribution of EGFR and ErbB-3 Heterodimerization to the EGFR Mutation-Induced Gefitinib- and Erlotinib-Resistance in Non-Small-Cell Lung Carcinoma TreatmentsStructure-based network analysis of activation mechanisms in the ErbB family of receptor tyrosine kinases: the regulatory spine residues are global mediators of structural stability and allosteric interactions.MuPIT interactive: webserver for mapping variant positions to annotated, interactive 3D structures.Computational modeling of allosteric communication reveals organizing principles of mutation-induced signaling in ABL and EGFR kinases.Verteporfin exhibits YAP-independent anti-proliferative and cytotoxic effects in endometrial cancer cellsComputational analyses of curcuminoid analogs against kinase domain of HER2Different epidermal growth factor (EGF) receptor ligands show distinct kinetics and biased or partial agonism for homodimer and heterodimer formation.Kinase activator-receiver preference in ErbB heterodimers is determined by intracellular regions and is not coupled to extracellular asymmetry.The ErbB4 CYT2 variant protects EGFR from ligand-induced degradation to enhance cancer cell motility.Phosphorylation of mutationally introduced tyrosine in the activation loop of HER2 confers gain-of-function activity.Regulation of the catalytic activity of the EGF receptor.A structural perspective on the regulation of the epidermal growth factor receptor.A systematic analysis of the resistance and sensitivity of HER2YVMA receptor tyrosine kinase mutant to tyrosine kinase inhibitors in HER2-positive lung cancer.Structure-Activity Relationship of Indole-Tethered Pyrimidine Derivatives that Concurrently Inhibit Epidermal Growth Factor Receptor and Other Angiokinases.ψ-Bufarenogin, a novel anti-tumor compound, suppresses liver cancer growth by inhibiting receptor tyrosine kinase-mediated signaling.Structural analysis of the EGFR/HER3 heterodimer reveals the molecular basis for activating HER3 mutationsPhase I first-in-human study of TAK-285, a novel investigational dual HER2/EGFR inhibitor, in cancer patients.Navigating into the binding pockets of the HER family protein kinases: discovery of novel EGFR inhibitor as antitumor agent.Combined 3D-QSAR modeling and molecular docking study on multi-acting quinazoline derivatives as HER2 kinase inhibitors.Structural Basis for the Non-catalytic Functions of Protein Kinases.Lapatinib and potential prognostic value of EGFR mutations in a Gynecologic Oncology Group phase II trial of persistent or recurrent endometrial cancerHER2 stabilizes EGFR and itself by altering autophosphorylation patterns in a manner that overcomes regulatory mechanisms and promotes proliferative and transformation signaling.Statistical analysis of EGFR structures' performance in virtual screening.Cancer Signature Investigation: ERBB2 (HER2)-Activating Mutation and Amplification-Positive Breast Carcinoma Mimicking Lung Primary.Activating Mutations in ERBB2 and Their Impact on Diagnostics and Treatment.Acquired substrate preference for GAB1 protein bestows transforming activity to ERBB2 kinase lung cancer mutants.Molecular basis for multimerization in the activation of the epidermal growth factor receptorAntitumor Activity of TAK-285, an Investigational, Non-Pgp Substrate HER2/EGFR Kinase Inhibitor, in Cultured Tumor Cells, Mouse and Rat Xenograft Tumors, and in an HER2-Positive Brain Metastasis Model.Carboxyl group footprinting mass spectrometry and molecular dynamics identify key interactions in the HER2-HER3 receptor tyrosine kinase interface.Destabilization of the epidermal growth factor receptor (EGFR) by a peptide that inhibits EGFR binding to heat shock protein 90 and receptor dimerization.Dynamic analysis of the epidermal growth factor (EGF) receptor-ErbB2-ErbB3 protein network by luciferase fragment complementation imagingCentrosomal kinase Nek2 cooperates with oncogenic pathways to promote metastasisDevelopment of novel HER2 inhibitors against gastric cancer derived from flavonoid source of Syzygium alternifolium through molecular dynamics and pharmacophore-based screening.
P2860
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P2860
Structural Analysis of the Mechanism of Inhibition and Allosteric Activation of the Kinase Domain of HER2 Protein
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@ast
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@en
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@nl
type
label
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@ast
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@en
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@nl
prefLabel
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@ast
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@en
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@nl
P2093
P2860
P3181
P356
P1476
Structural Analysis of the Mec ...... Kinase Domain of HER2 Protein
@en
P2093
Aki Hirokawa
Andy Jennings
Bi-Ching Sang
Gyorgy Snell
Hiroshi Miki
Jason Yano
Kathleen Aertgeerts
Keiji Iwamoto
Noriyuki Habuka
P2860
P304
P3181
P356
10.1074/JBC.M110.206193
P407
P577
2011-05-27T00:00:00Z