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Structural and Biochemical Bases for the Inhibition of Autophagy and Apoptosis by Viral BCL-2 of Murine γ-Herpesvirus 68Structural studies of a bacterial condensin complex reveal ATP-dependent disruption of intersubunit interactionsCrystal structures and enzyme mechanisms of a dual fucose mutarotase/ribose pyranaseEvidence that inhibition of BAX activation by BCL-2 involves its tight and preferential interaction with the BH3 domain of BAXMolecular basis for unidirectional scaffold switching of human Plk4 in centriole biogenesisStructural basis for the dephosphorylating activity of PTPRQ towards phosphatidylinositide substratesStructural basis of intersubunit recognition in elongin BC-cullin 5-SOCS box ubiquitin-protein ligase complexesThe family-wide structure and function of human dual-specificity protein phosphatasesStructural analysis of the polo-box domain of human Polo-like kinase 2Crystal structure of SP-PTP, a low molecular weight protein tyrosine phosphatase from Streptococcus pyogenesIdentification of a Highly Conserved Hypothetical Protein TON_0340 as a Probable Manganese-Dependent PhosphataseMitochondrial Akt Regulation of Hypoxic Tumor ReprogrammingAutophagic and tumour suppressor activity of a novel Beclin1-binding protein UVRAGPhosphoinositides differentially regulate protrudin localization through the FYVE domainDownregulation of autophagy by Bcl-2 promotes MCF7 breast cancer cell growth independent of its inhibition of apoptosis.Identification of novel protein tyrosine phosphatase sigma inhibitors promoting neurite extension.Structural Study of the HD-PTP Bro1 Domain in a Complex with the Core Region of STAM2, a Subunit of ESCRT-0.Conversion of cell-survival activity of Akt into apoptotic death of cancer cells by two mutations on the BIM BH3 domain.Crystal structures of two forms of the Acanthamoeba polyphaga mimivirus Rab GTPase.Structural and biochemical analysis of atypically low dephosphorylating activity of human dual-specificity phosphatase 28.Methyl 3-(3-(4-(2,4,4-Trimethylpentan-2-yl)phenoxy)-propanamido)benzoate as a Novel and Dual Malate Dehydrogenase (MDH) 1/2 Inhibitor Targeting Cancer Metabolism.Two-track virtual screening approach to identify both competitive and allosteric inhibitors of human small C-terminal domain phosphatase 1.High-resolution crystal structure of the PDZ1 domain of human protein tyrosine phosphatase PTP-Bas.Structural study reveals the temperature-dependent conformational flexibility of Tk-PTP, a protein tyrosine phosphatase from Thermococcus kodakaraensis KOD1.Structural and Physiological Exploration of Typhi YfdX Uncovers Its Dual Function in Bacterial Antibiotic Stress and VirulenceRequirement of the Cep57-Cep63 interaction for proper Cep152 recruitment and centriole duplicationOligomer Model of PB1 Domain of p62/SQSTM1 Based on Crystal Structure of Homo-Dimer and Calculation of Helical CharacteristicsIdentification of N-(5-(phenoxymethyl)-1,3,4-thiadiazol-2-yl)acetamide derivatives as novel protein tyrosine phosphatase epsilon inhibitors exhibiting anti-osteoclastic activityStructural basis for recognition of the tumor suppressor protein PTPN14 by the oncoprotein E7 of human papillomavirusDisordered region of cereblon is required for efficient degradation by proteolysis-targeting chimera
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
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name
Bonsu Ku
@ast
Bonsu Ku
@en
Bonsu Ku
@es
Bonsu Ku
@nl
type
label
Bonsu Ku
@ast
Bonsu Ku
@en
Bonsu Ku
@es
Bonsu Ku
@nl
prefLabel
Bonsu Ku
@ast
Bonsu Ku
@en
Bonsu Ku
@es
Bonsu Ku
@nl
P108
P106
P1153
14033375100
P31
P496
0000-0003-1784-8975