sameAs
Strictosidine synthase: mechanism of a Pictet-Spengler catalyzing enzymeNew developments in engineering plant metabolic pathwaysDevelopment of transcriptomic resources for interrogating the biosynthesis of monoterpene indole alkaloids in medicinal plant speciesAn old yellow enzyme gene controls the branch point between Aspergillus fumigatus and Claviceps purpurea ergot alkaloid pathways.A stereoselective hydroxylation step of alkaloid biosynthesis by a unique cytochrome P450 in Catharanthus roseus.Differential iridoid production as revealed by a diversity panel of 84 cultivated and wild blueberry species.The evolution of function in strictosidine synthase-like proteins.The impact of structural biology on alkaloid biosynthesis research.A three enzyme system to generate the Strychnos alkaloid scaffold from a central biosynthetic intermediate.Opportunities in metabolic engineering to facilitate scalable alkaloid production.Genome-guided investigation of plant natural product biosynthesis.Dual Catalytic Activity of a Cytochrome P450 Controls Bifurcation at a Metabolic Branch Point of Alkaloid Biosynthesis in Rauwolfia serpentina.Conversion of substrate analogs suggests a Michael cyclization in iridoid biosynthesis.A pair of tabersonine 16-hydroxylases initiates the synthesis of vindoline in an organ-dependent manner in Catharanthus roseus.Structural characterization of EasH (Aspergillus japonicus) - an oxidase involved in cycloclavine biosynthesis.Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity.Discovery and reconstitution of the cycloclavine biosynthetic pathway--enzymatic formation of a cyclopropyl group.Bypassing stereoselectivity in the early steps of alkaloid biosynthesis.Discovery of a short chain dehydrogenase from Catharanthus roseus that produces a novel monoterpene indole alkaloid.Redesign of a central enzyme in alkaloid biosynthesis.Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle.Cytochrome P450 and -methyltransferase catalyze the final steps in the biosynthesis of the anti-addictive alkaloid ibogaine fromSarpagan bridge enzyme has substrate-controlled cyclization and aromatization modesUncoupled activation and cyclization in catmint reductive terpenoid biosynthesis.Structural basis of cycloaddition in biosynthesis of iboga and aspidosperma alkaloidsBiocatalytic Strategies towards [4+2] CycloadditionsBeyond the semi-synthetic artemisinin: metabolic engineering of plant-derived anti-cancer drugsBiosynthesis of an Anti-Addiction Agent from the Iboga PlantThe evolutionary origins of the cat attractant nepetalactone in catnip
P50
Q24612814-CC5D8367-00B1-4556-8369-2182B3F4D6FFQ26748799-7E583A85-584B-4562-91EC-2F5820A1DF6DQ28484564-DCBBD1CE-D27E-4019-A083-C00DD769DF5BQ33946536-C9EA1C8E-92C3-4373-81A2-FA5131E2AB1FQ34947534-BE975815-366E-4239-BBD3-C30F9D6DA29DQ36400466-3FE9F222-DE93-449B-8A82-ED7BE10B26E9Q36580708-2D426FA8-2F12-4E01-A1BF-7673A0DFD444Q38036168-CDD01379-43A2-47F4-AF04-E09D057025DCQ38615215-AE1E8C27-05BA-43A6-BB3A-211FDF10064EQ39859222-7DB03352-A562-4EFC-BD1F-F372AE172240Q41378077-8D0DFCA7-8BEE-4454-8015-4BE091A10F10Q41602091-005378D3-F1B4-43D9-ABFB-1C42C31C3359Q42095945-3AACFCE2-F5E0-4E38-A1C9-A96770240939Q42263792-E98793E7-F28E-47E1-BFE3-C8D20F7DB5C8Q42320671-A6248521-D643-434A-BA8A-4C45C2754DECQ42416822-0466B76E-E6B8-43A5-AD03-D566B26F2627Q42425709-3F8FBCD7-05D8-4B40-B0AA-2061A7EB58BCQ42571491-3515C764-497E-4B02-9002-00AF939E1853Q50100612-D0119F4E-B88C-4DAD-A7BD-248408EEE13CQ51102596-10EE9A6A-9D73-4BE8-A352-36B493365945Q53686373-61B5353C-DD35-4714-992B-D337E0E2172DQ59339903-7A134859-421E-47AF-8167-A9510CCDA2DAQ59339911-8A262038-4433-4FDD-8C1A-2278094CF4DDQ64990657-367C26EB-A040-427D-9751-EF41F95821ADQ89748678-8CF6CA23-AE7D-457A-BEB9-15EFA30A44EBQ91140234-CB20B47B-E38B-42F7-A845-6F11530B7692Q92008828-78C9A16B-1C8F-455F-9894-737611C060BAQ92307708-82938569-B6C4-40EE-89A3-70E8C569CC33Q95279994-7A3DE439-F5B3-4DCB-B0D2-9C28B70E79AA
P50
description
American molecular biologist
@en
Amerikaans onderzoekster
@nl
US-amerikanische Naturstoffchemikerin
@de
bióloga molecular estadounidense
@es
հետազոտող
@hy
name
Sarah O'Connor
@en
Sarah O'Connor
@es
Sarah O'Connor
@nl
Sarah O'Connor
@sl
Sarah O’Connor
@de
سارة أوكونور
@ar
type
label
Sarah O'Connor
@en
Sarah O'Connor
@es
Sarah O'Connor
@nl
Sarah O'Connor
@sl
Sarah O’Connor
@de
سارة أوكونور
@ar
altLabel
Sarah E. O'Connor
@en
Sarah E. O'Connor
@nl
Sarah E. O’Connor
@de
prefLabel
Sarah O'Connor
@en
Sarah O'Connor
@es
Sarah O'Connor
@nl
Sarah O'Connor
@sl
Sarah O’Connor
@de
سارة أوكونور
@ar
P1053
O-5850-2016
P106
P166
P2080
P21
P31
P3829
P496
0000-0003-0356-6213
P569
1950-01-01T00:00:00Z