about
Cyclic Peptides Arising by Evolutionary Parallelism via Asparaginyl-Endopeptidase-Mediated BiosynthesisThe Arabidopsis B3 Domain Protein VERNALIZATION1 (VRN1) Is Involved in Processes Essential for Development, with Structural and Mutational Studies Revealing Its DNA-binding SurfaceEvolutionary Origins of a Bioactive Peptide Buried within PreproalbuminNatural structural diversity within a conserved cyclic peptide scaffoldDiverse cyclic seed peptides in the Mexican zinnia (Zinnia haageana).The alpine violet, Viola biflora, is a rich source of cyclotides with potent cytotoxicity.Identification of candidates for cyclotide biosynthesis and cyclisation by expressed sequence tag analysis of Oldenlandia affinisCycloquest: identification of cyclopeptides via database search of their mass spectra against genome databases.Vernalization requires epigenetic silencing of FLC by histone methylation.Cyclotides associate with leaf vasculature and are the products of a novel precursor in petunia (Solanaceae)Multiple pathways in the decision to flower: enabling, promoting, and resetting.Cyclotide isolation and characterization.Next generation sequencing and de novo transcriptomics to study gene evolution.LHP1, the Arabidopsis homologue of HETEROCHROMATIN PROTEIN1, is required for epigenetic silencing of FLCCircular proteins from Melicytus (Violaceae) refine the conserved protein and gene architecture of cyclotides.The evolution of Momordica cyclic peptides.Epigenetic regulation in the control of flowering.Cyclotides: macrocyclic peptides with applications in drug design and agriculture.Herbicidal properties of antimalarial drugs.Cyclotides as a basis for drug design.DNA Gyrase Is the Target for the Quinolone Drug Ciprofloxacin in Arabidopsis thaliana.An interactive database to explore herbicide physicochemical properties.A tripartite approach identifies the major sunflower seed albumins.Orientation and Location of the Cyclotide Kalata B1 in Lipid Bilayers Revealed by Solid-State NMR.Macrocyclization by asparaginyl endopeptidases.Peptide macrocyclization by a bifunctional endoprotease.Physical clustering of FLC alleles during Polycomb-mediated epigenetic silencing in vernalization.Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis.Expression, purification and preliminary X-ray diffraction studies of VERNALIZATION1(208-341) from Arabidopsis thaliana.Albumins and their processing machinery are hijacked for cyclic peptides in sunflower.ARABIDOPSIS TRITHORAX1 dynamically regulates FLOWERING LOCUS C activation via histone 3 lysine 4 trimethylation.Evidence for Ancient Origins of Bowman-Birk Inhibitors from Selaginella moellendorffii.Structural basis of ribosomal peptide macrocyclization in plants.Exploiting the Evolutionary Relationship between Malarial Parasites and Plants To Develop New Herbicides.A herbicide structure-activity analysis of the antimalarial lead compound MMV007978 against Arabidopsis thaliana.Developing ciprofloxacin analogues against plant DNA gyrase: a novel herbicide mode of action.Two proteins for the price of one: Structural studies of the dual-destiny protein preproalbumin with sunflower trypsin inhibitor-1.Cyclotides are a component of the innate defense of Oldenlandia affinis.Discovery of cyclotide-like protein sequences in graminaceous crop plants: ancestral precursors of circular proteins?Buried treasure: biosynthesis, structures and applications of cyclic peptides hidden in seed storage albumins.
P50
Q27670873-31A7B34D-6B87-412F-B50A-E6C45F5875AAQ27675549-605B058E-70B0-4EA7-8314-742E049199D2Q27682640-D5605D97-D15E-4FB4-9BB6-E1D37A5EE95DQ27728164-6FD9E166-AFD3-4CEB-9C84-58AE0063EA15Q31111152-DB3B84F3-AD3B-4A5E-93B7-EE48E6E708AFQ33314505-AE70BFAB-2AC7-491D-BE8B-B500D50EE204Q33531558-A0E21832-7F7F-4EB3-A166-5BEA6048AFD4Q33995951-24331DB2-F6BA-4E48-B6AC-A41C75469F40Q34288707-95B95674-86F9-4E42-80A4-39DE07E01CDAQ34304827-19E5028F-6073-4179-8B21-1278EEE35B57Q34307942-8A172F60-414F-4928-829A-C38F8648E6B1Q34433160-94C5840C-D82C-425B-AA8F-FEEAD4670A40Q34436510-65CAE75B-5B55-4752-8A9E-D20A073C395FQ34596813-DF957CBD-1205-4B7F-897B-B1C4EB02C81FQ34982528-863F2BB8-D5B6-46FC-A0F3-19409AFFAC12Q35400491-701BF632-C847-499F-A396-FF10398A0539Q36238660-8BA5B7D0-5F16-4674-B4E2-AA9E69CBCF6FQ37606347-90D5EA34-9EAC-4E89-8988-E3C91D679FD3Q37731378-0AF35E67-7909-4BD9-BBDD-12638CEB6E9BQ37999102-459BC04B-29F5-4592-BC9B-3AA92564AB49Q38377745-480A60FC-4FB8-411C-AA71-29565D0653EEQ38431382-513A6CC3-28C6-4F94-A9E7-17ACACC4D2C0Q38920769-EF44B9F7-AB6D-4C63-8058-719A68BA6716Q38931542-3BC592E8-6AFA-4840-A958-CAF6A87E86DEQ39189556-90B38E37-373F-4FF2-8714-9F2910B578ACQ40954576-CA401B2D-D211-4895-9F61-7BC401772695Q42641564-B487D768-09FC-46E9-AB51-6154DCFBA2A7Q42709448-6401CEAF-2938-4A62-A018-E6BCE85D96ABQ43170018-1D6AE1D0-E11E-4EC3-95DF-6FD8DAE7B349Q43418019-6A69DD16-700C-4D01-825E-E4A681D3CED0Q46674697-B963CAD3-4702-4F3C-96E5-A317AE6789EDQ47227488-78FFF800-3E13-4993-A1AD-D603CFC82C7BQ47694554-6A7B7BD7-58DB-4E12-A753-F1C308739A3EQ47998477-8A24624B-81AB-4A7E-96E2-D283914D1431Q48023693-99FDEF01-7C7C-491F-9ED6-C06DD9E5598DQ48042581-F50FFF1C-1EBA-47D3-8A39-E6FC463729AEQ48061034-473F0FE9-9B58-46F4-BC4C-9E1741B6BC88Q48064334-36F58AD8-4AAC-4181-AD80-75A22CBF6F93Q48085095-0CF1BF40-D2C9-4FFC-891E-D503F3F55D99Q48145790-4D322A78-C520-4EC7-AFCB-4F9837F1A059
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Joshua S. Mylne
@ast
Joshua S. Mylne
@en
Joshua S. Mylne
@es
Joshua S. Mylne
@nl
Joshua S. Mylne
@sl
type
label
Joshua S. Mylne
@ast
Joshua S. Mylne
@en
Joshua S. Mylne
@es
Joshua S. Mylne
@nl
Joshua S. Mylne
@sl
altLabel
Joshua S Mylne
@en
prefLabel
Joshua S. Mylne
@ast
Joshua S. Mylne
@en
Joshua S. Mylne
@es
Joshua S. Mylne
@nl
Joshua S. Mylne
@sl
P1053
A-5581-2009
P106
P1153
6507037056
P21
P31
P3829
P496
0000-0003-4957-6388