VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q39769935 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000316.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q39769935‏
024 ‎‡a 0000-0003-1979-5918‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q39769935‏
100 0 ‎‡a David A Robinson‏ ‎‡9 ast‏ ‎‡9 it‏ ‎‡9 sl‏ ‎‡9 es‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
400 0 ‎‡a ডেভিড এ রবিনসন‏ ‎‡c গবেষক‏ ‎‡9 bn‏
400 0 ‎‡a David A Robinson‏ ‎‡c researcher (ORCID 0000-0003-1979-5918)‏ ‎‡9 en‏
400 0 ‎‡a David A Robinson‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's A Molecular Hybridization Approach for the Design of Potent, Highly Selective, and Brain-Penetrant N-Myristoyltransferase Inhibitors‏
670 ‎‡a Author's Bisubstrate UDP–peptide conjugates as human O-GlcNAc transferase inhibitors‏
670 ‎‡a Author's Chemical Validation of Methionyl-tRNA Synthetase as a Druggable Target in Leishmania donovani‏
670 ‎‡a Author's Crystal structures of Helicobacter pylori type II dehydroquinase inhibitor complexes: new directions for inhibitor design‏
670 ‎‡a Author's Design and Synthesis of Brain Penetrant Trypanocidal N-Myristoyltransferase Inhibitors.‏
670 ‎‡a Author's Design, synthesis and biological evaluation of novel inhibitors of Trypanosoma brucei pteridine reductase 1.‏
670 ‎‡a Author's Development and validation of a cytochrome c-coupled assay for pteridine reductase 1 and dihydrofolate reductase‏
670 ‎‡a Author's Development of Small-Molecule Trypanosoma brucei N-Myristoyltransferase Inhibitors: Discovery and Optimisation of a Novel Binding Mode.‏
670 ‎‡a Author's Discovery of a Novel Class of Orally Active Trypanocidal N -Myristoyltransferase Inhibitors‏
670 ‎‡a Author's Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution‏
670 ‎‡a Author's Identification and structure solution of fragment hits against kinetoplastid N-myristoyltransferase‏
670 ‎‡a Author's Identification of inhibitors of an unconventional Trypanosoma brucei kinetochore kinase.‏
670 ‎‡a Author's Lead optimization of a pyrazole sulfonamide series of Trypanosoma brucei N-myristoyltransferase inhibitors: identification and evaluation of CNS penetrant compounds as potential treatments for stage 2 human African trypanosomiasis‏
670 ‎‡a Author's Lysyl-tRNA synthetase as a drug target in malaria and cryptosporidiosis‏
670 ‎‡a Author's Mechanism of Enzymatic Fluorination in Streptomyces c attleya‏
670 ‎‡a Author's N-myristoyltransferase inhibitors as new leads to treat sleeping sickness‏
670 ‎‡a Author's N-myristoyltransferase is a cell wall target in Aspergillus fumigatus‏
670 ‎‡a Author's Novel Ligands for a Purine Riboswitch Discovered by RNA-Ligand Docking‏
670 ‎‡a Author's O-GlcNAc transferase invokes nucleotide sugar pyrophosphate participation in catalysis‏
670 ‎‡a Author's One Scaffold, Three Binding Modes: Novel and Selective Pteridine Reductase 1 Inhibitors Derived from Fragment Hits Discovered by Virtual Screening‏
670 ‎‡a Author's Phosphorylation of Sli15 by Ipl1 is important for proper CPC localization and chromosome stability in Saccharomyces cerevisiae.‏
670 ‎‡a Author's Structure-guided design of Alpha -amino acid-derived Pin1 inhibitors‏
670 ‎‡a Author's Substrate specificity in enzymatic fluorination. The fluorinase from Streptomyces cattleya accepts 2'-deoxyadenosine substrates‏
670 ‎‡a Author's Targeting a critical step in fungal hexosamine biosynthesis‏
670 ‎‡a Author's The fluorinase from Streptomyces cattleya is also a chlorinase‏
670 ‎‡a Author's The histone chaperones Vps75 and Nap1 form ring-like, tetrameric structures in solution.‏
670 ‎‡a Author's Type II dehydroquinase: molecular replacement with many copies‏
909 ‎‡a (orcid) 0000000319795918‏ ‎‡9 1‏
919 ‎‡a molecularhybridizationapproachforthedesignofpotenthighlyselectiveandbrainpenetrantnmyristoyltransferaseinhibitors‏ ‎‡A A Molecular Hybridization Approach for the Design of Potent, Highly Selective, and Brain-Penetrant N-Myristoyltransferase Inhibitors‏ ‎‡9 1‏
919 ‎‡a bisubstrateudppeptideconjugatesashumanoglcnactransferaseinhibitors‏ ‎‡A Bisubstrate UDP–peptide conjugates as human O-GlcNAc transferase inhibitors‏ ‎‡9 1‏
919 ‎‡a chemicalvalidationofmethionyltrnasynthetaseasadruggabletargetinleishmaniadonovani‏ ‎‡A Chemical Validation of Methionyl-tRNA Synthetase as a Druggable Target in Leishmania donovani‏ ‎‡9 1‏
919 ‎‡a crystalstructuresofhelicobacterpyloritype2dehydroquinaseinhibitorcomplexesnewdirectionsforinhibitordesign‏ ‎‡A Crystal structures of Helicobacter pylori type II dehydroquinase inhibitor complexes: new directions for inhibitor design‏ ‎‡9 1‏
919 ‎‡a designandsynthesisofbrainpenetranttrypanocidalnmyristoyltransferaseinhibitors‏ ‎‡A Design and Synthesis of Brain Penetrant Trypanocidal N-Myristoyltransferase Inhibitors.‏ ‎‡9 1‏
919 ‎‡a designsynthesisandbiologicalevaluationofnovelinhibitorsoftrypanosomabruceipteridinereductase1‏ ‎‡A Design, synthesis and biological evaluation of novel inhibitors of Trypanosoma brucei pteridine reductase 1.‏ ‎‡9 1‏
919 ‎‡a developmentandvalidationofacytochrome100coupledassayforpteridinereductase1anddihydrofolatereductase‏ ‎‡A Development and validation of a cytochrome c-coupled assay for pteridine reductase 1 and dihydrofolate reductase‏ ‎‡9 1‏
919 ‎‡a developmentofsmallmoleculetrypanosomabruceinmyristoyltransferaseinhibitorsdiscoveryandoptimisationofanovelbindingmode‏ ‎‡A Development of Small-Molecule Trypanosoma brucei N-Myristoyltransferase Inhibitors: Discovery and Optimisation of a Novel Binding Mode.‏ ‎‡9 1‏
919 ‎‡a discoveryofanovelclassoforallyactivetrypanocidalnmyristoyltransferaseinhibitors‏ ‎‡A Discovery of a Novel Class of Orally Active Trypanocidal N -Myristoyltransferase Inhibitors‏ ‎‡9 1‏
919 ‎‡a discoveryofcellactivephenylimidazolepin1inhibitorsbystructureguidedfragmentevolution‏ ‎‡A Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution‏ ‎‡9 1‏
919 ‎‡a identificationandstructuresolutionoffragmenthitsagainstkinetoplastidnmyristoyltransferase‏ ‎‡A Identification and structure solution of fragment hits against kinetoplastid N-myristoyltransferase‏ ‎‡9 1‏
919 ‎‡a identificationofinhibitorsofanunconventionaltrypanosomabruceikinetochorekinase‏ ‎‡A Identification of inhibitors of an unconventional Trypanosoma brucei kinetochore kinase.‏ ‎‡9 1‏
919 ‎‡a leadoptimizationofapyrazolesulfonamideseriesoftrypanosomabruceinmyristoyltransferaseinhibitorsidentificationandevaluationofcnspenetrantcompoundsaspotentialtreatmentsforstage2humanafricantrypanosomiasis‏ ‎‡A Lead optimization of a pyrazole sulfonamide series of Trypanosoma brucei N-myristoyltransferase inhibitors: identification and evaluation of CNS penetrant compounds as potential treatments for stage 2 human African trypanosomiasis‏ ‎‡9 1‏
919 ‎‡a lysyltrnasynthetaseasadrugtargetinmalariaandcryptosporidiosis‏ ‎‡A Lysyl-tRNA synthetase as a drug target in malaria and cryptosporidiosis‏ ‎‡9 1‏
919 ‎‡a mechanismofenzymaticfluorinationinstreptomyces100attleya‏ ‎‡A Mechanism of Enzymatic Fluorination in Streptomyces c attleya‏ ‎‡9 1‏
919 ‎‡a nmyristoyltransferaseinhibitorsasnewleadstotreatsleepingsickness‏ ‎‡A N-myristoyltransferase inhibitors as new leads to treat sleeping sickness‏ ‎‡9 1‏
919 ‎‡a nmyristoyltransferaseisacellwalltargetinaspergillusfumigatus‏ ‎‡A N-myristoyltransferase is a cell wall target in Aspergillus fumigatus‏ ‎‡9 1‏
919 ‎‡a novelligandsforapurineriboswitchdiscoveredbyrnaliganddocking‏ ‎‡A Novel Ligands for a Purine Riboswitch Discovered by RNA-Ligand Docking‏ ‎‡9 1‏
919 ‎‡a glcnactransferaseinvokesnucleotidesugarpyrophosphateparticipationincatalysis‏ ‎‡A O-GlcNAc transferase invokes nucleotide sugar pyrophosphate participation in catalysis‏ ‎‡9 1‏
919 ‎‡a 1scaffold3bindingmodesnovelandselectivepteridinereductase1inhibitorsderivedfromfragmenthitsdiscoveredbyvirtualscreening‏ ‎‡A One Scaffold, Three Binding Modes: Novel and Selective Pteridine Reductase 1 Inhibitors Derived from Fragment Hits Discovered by Virtual Screening‏ ‎‡9 1‏
919 ‎‡a phosphorylationofsli15byipl1isimportantforpropercpclocalizationandchromosomestabilityinsaccharomycescerevisiae‏ ‎‡A Phosphorylation of Sli15 by Ipl1 is important for proper CPC localization and chromosome stability in Saccharomyces cerevisiae.‏ ‎‡9 1‏
919 ‎‡a structureguideddesignof Alpha aminoacidderivedpin1inhibitors‏ ‎‡A Structure-guided design of Alpha -amino acid-derived Pin1 inhibitors‏ ‎‡9 1‏
919 ‎‡a substratespecificityinenzymaticfluorinationthefluorinasefromstreptomycescattleyaaccepts2deoxyadenosinesubstrates‏ ‎‡A Substrate specificity in enzymatic fluorination. The fluorinase from Streptomyces cattleya accepts 2'-deoxyadenosine substrates‏ ‎‡9 1‏
919 ‎‡a targetingacriticalstepinfungalhexosaminebiosynthesis‏ ‎‡A Targeting a critical step in fungal hexosamine biosynthesis‏ ‎‡9 1‏
919 ‎‡a fluorinasefromstreptomycescattleyaisalsoachlorinase‏ ‎‡A The fluorinase from Streptomyces cattleya is also a chlorinase‏ ‎‡9 1‏
919 ‎‡a histonechaperonesvps75andnap1formringliketetramericstructuresinsolution‏ ‎‡A The histone chaperones Vps75 and Nap1 form ring-like, tetrameric structures in solution.‏ ‎‡9 1‏
919 ‎‡a type2dehydroquinasemolecularreplacementwithmanycopies‏ ‎‡A Type II dehydroquinase: molecular replacement with many copies‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
996 ‎‡2 ISNI|0000000067775290‏
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996 ‎‡2 NSK|000046870‏
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996 ‎‡2 J9U|987007424518505171‏
996 ‎‡2 LC|n 2007085367‏
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996 ‎‡2 NYNYRILM|394980‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏