about
(4-aminomethyl)phenylguanidine derivatives as nonpeptidic highly selective inhibitors of human urokinaseA gated channel into the proteasome core particleMutational studies on HslU and its docking mode with HslVStructural plasticity and noncovalent substrate binding in the GroEL apical domain. A study using electrospay ionization mass spectrometry and fluorescence binding studiesExpansion of the genetic code enables design of a novel "gold" class of green fluorescent proteinsSynthetic Biology of Proteins: Tuning GFPs Folding and Stability with FluoroprolineEvidence for a direct interaction between the penultimate aspartic acid of cholecystokinin and histidine 207, located in the second extracellular loop of the cholecystokinin B receptorIdentification of tyrosine 189 and asparagine 358 of the cholecystokinin 2 receptor in direct interaction with the crucial C-terminal amide of cholecystokinin by molecular modeling, site-directed mutagenesis, and structure/affinity studiesProteins with beta-(thienopyrrolyl)alanines as alternative chromophores and pharmaceutically active amino acidsStructural and spectral response of Aequorea victoria green fluorescent proteins to chromophore fluorination.Synthetic biology of protein folding.Photomodulation of conformational states. III. Water-soluble bis-cysteinyl-peptides with (4-aminomethyl) phenylazobenzoic acid as backbone constituent.Practical aspects of the 2D 15N-[1h]-NOE experiment.Micellar environments induce structuring of the N-terminal tail of the prion protein.A new method to determine the structure of the metal environment in metalloproteins: investigation of the prion protein octapeptide repeat Cu(2+) complex.Structure of cholecystokinin receptor binding sites and mechanism of activation/inactivation by agonists/antagonists.Copper binding and conformation of the N-terminal octarepeats of the prion protein in the presence of DPC micelles as membrane mimetic.Arginine 336 and asparagine 333 of the human cholecystokinin-A receptor binding site interact with the penultimate aspartic acid and the C-terminal amide of cholecystokinin.A photocontrolled beta-hairpin peptide.Degradation of cholecystokinin octapeptide, related fragments and analogs by human and rat plasma in vitro.Design and synthesis of heterotrimeric collagen peptides with a built-in cystine-knot. Models for collagen catabolism by matrix-metalloproteases.Identification of two amino acids of the human cholecystokinin-A receptor that interact with the N-terminal moiety of cholecystokinin.Synthetic heterotrimeric collagen peptides as mimics of cell adhesion sites of the basement membrane.Azobenzene as conformational switch in model peptides.Natural and artificial cystine knots for assembly of homo- and heterotrimeric collagen models.Design of anti- and pro-aggregation variants to assess the effects of methionine oxidation in human prion protein.Insulin-From its Discovery to the Industrial Synthesis of Modern Insulin Analogues.The configuration of the Cu(2+) binding region in full-length human prion protein compared with the isolated octapeptide.A new cell-permeable calpain inhibitor.Ultrafast conformational dynamics in cyclic azobenzene peptides of increased flexibility.Calpastatin exon 1B-derived peptide, a selective inhibitor of calpain: enhancing cell permeability by conjugation with penetratin.Peptide hormone-membrane interactions: the aggregational and conformational state of lipo-gastrin derivatives and their receptor binding affinity.Crystal structure of NS-134 in complex with bovine cathepsin B: a two-headed epoxysuccinyl inhibitor extends along the entire active-site cleft.Interaction of PHM, PHI and 24-glutamine PHI with human VIP receptors from colonic epithelium: comparison with rat intestinal receptors.The disulfide-coupled folding pathway of apamin as derived from diselenide-quenched analogs and intermediates.Pharmacological and biochemical evidence for the simultaneous expression of CCKB/gastrin and CCKA receptors in the pig pancreasSynthesis of human des-tryptophan-1,norleucine-12-minigastrin-II and its biological activities.1-(tert-butylthio)-1,2-hydrazinedicarboxylic acid derivatives. New reagents for the introduction of the S-tert-butylthio group into cysteine and cysteine derivatives.Evidence for a direct and functional interaction between the regulators of G protein signaling-2 and phosphorylated C terminus of cholecystokinin-2 receptor.Multiple loop conformations of peptides predicted by molecular dynamics simulations are compatible with nuclear magnetic resonance.
P50
Q27622497-AA55C2C0-62B6-427A-A359-99EE143AD552Q27627907-52555F5C-008C-449E-92CE-1EDCEA29F38BQ27628887-179D4431-62ED-43EB-9D00-B6A01D074173Q27639174-73FA468A-FCD7-4B6D-8FDB-4E9A797CF9B7Q27641115-3DF1077E-A14F-4A90-B52E-3453DEB01449Q27649939-B6F56810-2E52-4144-B98E-DE4A70AA3717Q28141454-694C6706-7201-4736-9B30-34DB13F092FBQ28191088-79D22C9F-E88B-4F82-A747-276C4AB257AEQ28367374-AF604424-B0D2-4AD2-877D-60C20F114B68Q30350324-02960144-2F9D-428D-A8A9-5468ECE2BD11Q30388062-FC275BAD-4F52-42A0-AF29-0AEB057D8B3DQ30683116-C1DFB5A0-4A36-46A9-ABF6-778C16067E62Q30697866-D5445685-111C-4778-9CC5-38D453D9936EQ30909287-4187D4A5-3F02-41E5-AF01-C52E5D48E5EDQ30966538-B1CE00C7-B260-49EE-AE91-7B02FDCFF833Q33186670-CD9D3656-66DD-456D-B5C7-94806972DF31Q33344720-741239DC-11CE-4701-98B6-93E66166A3CAQ33867566-36DB2754-532E-4D73-9731-82A2CE8F866DQ33991509-3F0B8EDB-3405-4C7F-BC1D-A2F3A8083CABQ34253816-3F9E73B7-D9B2-47F9-9D42-AA5174352122Q34409703-3A45B01F-D955-4657-9A89-C0F658C319D7Q34414258-5521B1C0-9CF9-48FE-95DA-586CDD716ED9Q35680922-ABE68249-DC2A-455F-B23C-1C5AC1E1D34AQ36461769-B2BBDF30-2743-41E8-A8FF-C7B553514A8CQ36981440-341A39E5-5E31-4438-A4FB-D4CC6F176435Q37172413-E21744A6-B5D0-4FC5-9966-CD6D98AD31FBQ39332512-0199FBB4-A75A-48D5-A59D-EDD1D3DE65E8Q40215947-B8C3A381-D261-4DF5-8D1D-612C0571991AQ40223788-85FBAD3A-0A3E-41D1-94C0-E8809F652DD0Q40278281-C7EB51E3-43C5-4764-8CDA-62DAD48F98F8Q40652159-E9243398-0B91-4C24-9D55-EE5F929D3ED3Q41595218-E90ADE2A-D814-43A6-AFA0-CB298A5ADCA5Q41845464-67A7848D-7A87-48C0-A08F-3C2F39CF3DE0Q41872532-3CF98EFB-5306-477B-BA88-1B2A3630226CQ41917718-1C9A745B-1B33-4587-BF18-9B2A2C4E3A02Q41965474-96C1B39C-8F3B-4E15-A0A5-33238BEABDB6Q42222250-85230443-3C0D-42AC-AA40-EE26F2DD196AQ42266022-A9AAC7D0-F0F0-4108-9659-C53B4F0D43EFQ42446135-9EF35683-99A1-485B-B6DF-CB2D0188E236Q42651256-DCC89467-FE2F-4ABB-B80F-E12BC0B894F5
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Luis Moroder
@ast
Luis Moroder
@en
Luis Moroder
@es
Luis Moroder
@nl
Luis Moroder
@sl
type
label
Luis Moroder
@ast
Luis Moroder
@en
Luis Moroder
@es
Luis Moroder
@nl
Luis Moroder
@sl
prefLabel
Luis Moroder
@ast
Luis Moroder
@en
Luis Moroder
@es
Luis Moroder
@nl
Luis Moroder
@sl
P106
P1153
7103123802
P21
P31
P496
0000-0001-9570-5713
P569
2000-01-01T00:00:00Z