sameAs
The Spirodela polyrhiza genome reveals insights into its neotenous reduction fast growth and aquatic lifestyleAzide and acetate complexes plus two iron-depleted crystal structures of the di-iron enzyme delta9 stearoyl-acyl carrier protein desaturase. Implications for oxygen activation and catalytic intermediatesThe crystal structure of the ivy Delta4-16:0-ACP desaturase reveals structural details of the oxidized active site and potential determinants of regioselectivityRemote control of regioselectivity in acyl-acyl carrier protein-desaturasesA family of metal-dependent phosphatases implicated in metabolite damage-controlResonance Raman evidence for an Fe-O-Fe center in stearoyl-ACP desaturase. Primary sequence identity with other diiron-oxo proteinsDESATURATION AND RELATED MODIFICATIONS OF FATTY ACIDS1Modification of the fatty acid composition of Escherichia coli by coexpression of a plant acyl-acyl carrier protein desaturase and ferredoxinEight histidine residues are catalytically essential in a membrane-associated iron enzyme, stearoyl-CoA desaturase, and are conserved in alkane hydroxylase and xylene monooxygenaseSurvey of the total fatty acid and triacylglycerol composition and content of 30 duckweed species and cloning of a Δ6-desaturase responsible for the production of γ-linolenic and stearidonic acids in Lemna gibbaCoexpressing Escherichia coli cyclopropane synthase with Sterculia foetida Lysophosphatidic acid acyltransferase enhances cyclopropane fatty acid accumulationFusing catalase to an alkane-producing enzyme maintains enzymatic activity by converting the inhibitory byproduct H2O2 to the cosubstrate O2Defective pollen wall is required for anther and microspore development in rice and encodes a fatty acyl carrier protein reductaseMale Sterile2 encodes a plastid-localized fatty acyl carrier protein reductase required for pollen exine development in ArabidopsisIdentification of amino acid residues involved in substrate specificity of plant acyl-ACP thioesterases using a bioinformatics-guided approachEvidence that the yeast desaturase Ole1p exists as a dimer in vivoCharacterization and analysis of the cotton cyclopropane fatty acid synthase family and their contribution to cyclopropane fatty acid synthesisA fatty acid desaturase modulates the activation of defense signaling pathways in plantsFAD2 and FAD3 desaturases form heterodimers that facilitate metabolic channeling in vivo.Red light-induced formation of ubiquitin-phytochrome conjugates: Identification of possible intermediates of phytochrome degradation.Efficient transformation and artificial miRNA gene silencing in Lemna minor.Modulating seed beta-ketoacyl-acyl carrier protein synthase II level converts the composition of a temperate seed oil to that of a palm-like tropical oilA single mutation in the castor Delta9-18:0-desaturase changes reaction partitioning from desaturation to oxidase chemistry.Engineering a monolignol 4-O-methyltransferase with high selectivity for the condensed lignin precursor coniferyl alcoholConjugated fatty acid synthesis: residues 111 and 115 influence product partitioning of Momordica charantia conjugaseFeedback regulation of plastidic acetyl-CoA carboxylase by 18:1-acyl carrier protein in Brassica napus.Mössbauer studies of alkane omega-hydroxylase: evidence for a diiron cluster in an integral-membrane enzymeParallel and competitive pathways for substrate desaturation, hydroxylation, and radical rearrangement by the non-heme diiron hydroxylase AlkB.Revealing the catalytic potential of an acyl-ACP desaturase: tandem selective oxidation of saturated fatty acids.Desaturases: emerging models for understanding functional diversification of diiron-containing enzymes.50 years of Arabidopsis research: highlights and future directions.Triacylglycerol Metabolism, Function, and Accumulation in Plant Vegetative Tissues.Cellular Organization of Triacylglycerol Biosynthesis in Microalgae.Expression of a functional monocotyledonous phytochrome in transgenic tobacco.Ubiquitin-phytochrome conjugates. Pool dynamics during in vivo phytochrome degradation.Metabolic engineering of seeds can achieve levels of omega-7 fatty acids comparable with the highest levels found in natural plant sources.Stereochemistry of 10-sulfoxidation catalyzed by a soluble Delta9 desaturase.Evidence linking the Pseudomonas oleovorans alkane omega-hydroxylase, an integral membrane diiron enzyme, and the fatty acid desaturase family.Immunochemically detectable phytochrome is present at normal levels but is photochemically nonfunctional in the hy 1 and hy 2 long hypocotyl mutants of Arabidopsis.A structural model of the plant acyl-acyl carrier protein thioesterase FatB comprises two helix/4-stranded sheet domains, the N-terminal domain containing residues that affect specificity and the C-terminal domain containing catalytic residues.
P50
Q22122095-DFEBD98D-9049-47A3-B710-ED05DF319240Q27641015-E98EA7EB-CA60-4023-A870-328F4C553838Q27644620-0EAAB8F1-75A7-4BD7-82E1-2946CD6EC481Q27674208-CE9917E8-833E-408C-8BBD-BCCD6A6C36B2Q27711952-B0056387-34B3-46DC-861E-612234200DAFQ28239823-DCE7B39F-416A-4663-A180-20EFA0EA8955Q28249518-8A1A5454-FFAF-4C03-A78E-DBECBF8A4C85Q28272559-5BB85BC4-C8AE-4FED-B6E4-0A9E87EA33F2Q28564292-9A131177-19AF-44EB-A496-CDBDC636D803Q28660888-FA1F1BC1-DF03-4F90-AA94-D354C6C0FA2CQ28660934-3C1266A8-740B-47BD-AC9D-9775CA93C2C4Q28706328-93A13851-C37D-4696-A7DE-40CCAFDC463BQ28741141-5A7D17A3-14D7-4EE5-8009-2538552AF473Q28743926-5802C1ED-48A1-4E42-9143-67AE2301102EQ33268095-48FBBBEE-EA1E-4E33-BF4B-833D59D3B315Q33911379-DFEB8769-4D53-42E9-9A58-0907C0E3D65EQ33911882-B2A703A4-ADC1-47F6-A7DC-6EF3F4EFBB6FQ33931488-F7AF69FA-66DE-4895-B2DD-D7463290577AQ34073870-802C830F-AE50-4FC3-B981-92F868372996Q34587835-BDF356AD-41AE-424E-BB9C-BD796040C151Q35690658-722C50EA-6F54-46E9-9875-6CB1E907B8AEQ35721808-FD2A255E-0176-482C-ADEA-3AE4B88FAB90Q35768543-01DF8118-F08E-4DE9-A008-1009E9085B70Q35778080-151FC267-CA0D-475C-A93A-C01FFAB0CDFEQ35956796-E5304AC9-07A4-413F-98E2-C0DB5290F3C8Q36056606-4E07C77A-ACAE-41EF-AAE2-E94FEDA3B824Q36073433-2EF8F153-4116-4A6A-9F66-A4E6BCF395C8Q36493437-247CFFA8-CD31-4BA9-97CA-0E572F10BDA9Q36936233-19418B6A-C7A9-44A8-A346-91D9322B84A9Q37254049-3915B795-1C91-4F47-9E6A-AB4164B13A44Q38606784-0457315E-1404-4AC3-81A6-69B9E88693EAQ38723112-D00670E9-3529-4BDE-ACE2-B788B7C27FFBQ38792248-E6D64288-286C-4FF2-9A38-CCD181AF07AAQ40817557-9EAD18DE-2867-4F6F-9EE8-E39FD1DDE0EDQ41268928-E4063F62-45DB-49AB-8C56-DE9BE35E51C8Q42859944-5D547AEA-3620-4880-90FC-CD0CB76E0577Q43142391-9B8C4D8A-7BBD-40C5-B3A4-9C85DA6F1294Q44476884-E699DD07-6E1B-4423-B125-73BBFF9CF8F8Q44895702-0DCAA449-4DC2-4513-967D-C6E1CAE3A376Q45142930-ADEEE3CD-62C8-47A8-A8D9-F490E4D61DA3
P50
description
biologist, and researcher
@en
bioloog
@nl
հետազոտող
@hy
name
John Shanklin
@ast
John Shanklin
@en
John Shanklin
@es
John Shanklin
@nl
John Shanklin
@sl
type
label
John Shanklin
@ast
John Shanklin
@en
John Shanklin
@es
John Shanklin
@nl
John Shanklin
@sl
prefLabel
John Shanklin
@ast
John Shanklin
@en
John Shanklin
@es
John Shanklin
@nl
John Shanklin
@sl
P69
P1153
7005779182
P21
P31
P496
0000-0002-6774-8043