about
De novo design, synthesis and solution conformational study of two didehydroundecapeptides: effect of nature and number of amino acids interspersed between ΔPhe residues.Spectroscopically labeled peptaibiotic analogs: the 4-nitrophenylalanine infrared absorption probe inserted at different positions into trichogin GA IV.An Ancestral Tryptophanyl-tRNA Synthetase Precursor Achieves High Catalytic Rate Enhancement without Ordered Ground-State Tertiary Structures.A peptide template as an allosteric supramolecular catalyst for the cleavage of phosphate esters.Facile biofunctionalization of silver nanoparticles for enhanced antibacterial properties, endotoxin removal, and biofilm control.Diffusion NMR spectroscopy: folding and aggregation of domains in p53.The rational search for selective anticancer derivatives of the peptide Trichogin GA IV: a multi-technique biophysical approach.Insights into peptide-membrane interactions of newly synthesized, nitroxide-containing analogs of the peptaibiotic trichogin GA IV using EPR.Chain length, temperature and solvent effects on the structural properties of α-aminoisobutyric acid homooligopeptides.4-Cyano-α-methyl-l-phenylalanine as a spectroscopic marker for the investigation of peptaibiotic-membrane interactions.An improved AMBER force field for α,α-dialkylated peptides: intrinsic and solvent-induced conformational preferences of model systems.C-terminal octylation rescues an inactive T20 mutant: implications for the mechanism of HIV/SIMIAN immunodeficiency virus-induced membrane fusion.New tools for the control of peptide conformation and supramolecular chemistry: crown-carrier, C(alpha)-methyl L-DOPA amino acids.Deracemization and the first CD spectrum of a 3(10)-helical peptide made of achiral α-amino-isobutyric acid residues in a chiral membrane mimetic environment.Solution synthesis, conformational analysis, and antimicrobial activity of three alamethicin F50/5 analogs bearing a trifluoroacetyl label.Synthesis, preferred conformation, protease stability, and membrane activity of heptaibin, a medium-length peptaibiotic.Synthesis and conformational properties of a TOAC doubly spin-labeled analog of the medium-length, membrane active peptaibiotic ampullosporin A as revealed by CD, fluorescence, and EPR spectroscopies.N-terminal diproline and charge group effects on the stabilization of helical conformation in alanine-based short peptides: CD studies with water and methanol as solvent.Stereocontrolled Synthesis of Quaternary β,γ-Unsaturated Amino Acids: Chain Extension of D- & L- α-(2-Tributylstannyl)Vinyl Amino Acids.Isovaline in naturally occurring peptides: A nondestructive methodology for configurational assignmentDiscriminating 310- from ?-helices: Vibrational and electronic CD and IR absorption study of related Aib-containing oligopeptides
P2860
Q30408143-2530D154-C02F-4002-A3A5-0D19DCD2B229Q30583903-B91B5792-E245-4D7E-8A34-ABEFA68661AEQ33770718-1A468A63-17F9-48EF-9098-7E6BE1DC8DC1Q34023672-44EAA801-6CFE-42E2-A7B9-304E3F957DFDQ35209785-5E1F382C-52F1-40FF-A540-3C6A4F230F43Q36247152-1F9CE4D4-D847-4CB5-ABE1-4A622E9A73ADQ38781250-7CA63F90-7104-4A0D-91E2-76FFB8154FB5Q39395882-6F2BCCC7-3B39-4246-89F0-2B1F0B3BD17FQ39612191-C20FBCC7-7A97-400F-B0AA-A22F0D91AE64Q41065597-308A66CF-AB15-4DD2-92DA-67BE6B8ACFBDQ44366449-A94FBFE2-9180-4DAE-AFF5-4D2E075BC08EQ44368570-B921C502-6F7A-4277-A18E-DC7E02F046AFQ44781096-56E4A697-26C2-45DE-8476-E369F704112BQ45399410-A2F9C9BA-9297-4D1B-AB9E-3417A6CC6C5CQ45881924-173C7706-1A6E-4496-AE1C-F8BA5F9EFD69Q46361123-6532674A-5A5F-4EB6-9331-9D91B4E5FD95Q47907234-3954B913-F9A2-403B-BA61-E34BC1CC5DA9Q48255419-59B2F3C6-F8A4-42C6-877E-4B6D32CCF43EQ55493799-913C25DF-4953-4AE2-AF82-29347B8221DCQ58440550-D2DB73C5-1B3D-44BF-B12B-E76A9C1E21A8Q58440903-BD8630A3-B563-4D4C-BBDC-6A38DA8A945F
P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
The first water-soluble 3(10)-helical peptides.
@ast
The first water-soluble 3(10)-helical peptides.
@en
type
label
The first water-soluble 3(10)-helical peptides.
@ast
The first water-soluble 3(10)-helical peptides.
@en
prefLabel
The first water-soluble 3(10)-helical peptides.
@ast
The first water-soluble 3(10)-helical peptides.
@en
P2093
P1476
The first water-soluble 3(10)-helical peptides.
@en
P2093
Broxterman QB
Formaggio F
Kamphuis J
P304
P356
10.1002/1521-3765(20001215)6:24<4498::AID-CHEM4498>3.0.CO;2-4
P407
P577
2000-12-01T00:00:00Z