scholarly article | Q13442814 |
P2093 | author name string | Ullrich B | |
Polgár L | |||
Szeltner Z | |||
Fidy J | |||
Laberge M | |||
Tölgyesi F | |||
P2860 | cites work | Experimentally verifying molecular dynamics simulations through fluorescence anisotropy measurements | Q68189233 |
Confirmation that multiexponential fluorescence decay behavior of holoazurin originates from conformational heterogeneity | Q69215504 | ||
Molecular dynamics simulation of HIV-1 protease in a crystalline environment and in solution | Q70556978 | ||
Solute perturbation of protein fluorescence. Quenching of the tryptophyl fluorescence of model compounds and of lysozyme by iodide ion | Q70598973 | ||
Conformational stability and catalytic activity of HIV-1 protease are both enhanced at high salt concentration | Q71058497 | ||
Unfolding pathway of apomyoglobin. Simultaneous characterization of acidic conformational states by frequency domain fluorometry | Q72109482 | ||
A fluorescence study of tryptophan-histidine interactions in the peptide anantin and in solution | Q72156376 | ||
Intrinsic tryptophan fluorescence identifies specific conformational changes at the actomyosin interface upon actin binding and ADP release | Q73141706 | ||
Time-resolved fluorescence anisotropy of HIV-1 protease inhibitor complexes correlates with inhibitory activity | Q74252390 | ||
Studies of the fluorescence from tryptophan in melittin | Q93659185 | ||
Active human immunodeficiency virus protease is required for viral infectivity | Q24647696 | ||
Human immunodeficiency virus has an aspartic-type protease that can be inhibited by pepstatin A | Q24649411 | ||
X-ray structure and conformational dynamics of the HIV-1 protease in complex with the inhibitor SDZ283-910: agreement of time-resolved spectroscopy and molecular dynamics simulations | Q27639832 | ||
Crystallographic analysis of a complex between human immunodeficiency virus type 1 protease and acetyl-pepstatin at 2.0-A resolution | Q27675151 | ||
Conserved folding in retroviral proteases: crystal structure of a synthetic HIV-1 protease | Q27696384 | ||
Three-dimensional structure of aspartyl protease from human immunodeficiency virus HIV-1 | Q27702268 | ||
X-ray analysis of HIV-1 proteinase at 2.7 A resolution confirms structural homology among retroviral enzymes | Q27703747 | ||
Hydrophilic peptides derived from the transframe region of Gag-Pol inhibit the HIV-1 protease | Q27748879 | ||
The interpretation of protein structures: Estimation of static accessibility | Q27860750 | ||
The Protein Data Bank: a computer-based archival file for macromolecular structures | Q27860989 | ||
A step toward the prediction of the fluorescence lifetimes of tryptophan residues in proteins based on structural and spectral data. | Q30326440 | ||
Quenching-resolved emission anisotropy studies with single and multitryptophan-containing proteins | Q30447215 | ||
Thermodynamic linkage between the binding of protons and inhibitors to HIV-1 protease | Q30480872 | ||
Inhibitors of HIV-1 protease: a major success of structure-assisted drug design | Q32059371 | ||
Probing alpha-helical secondary structure at a specific site in model peptides via restriction of tryptophan side-chain rotamer conformation | Q34115328 | ||
Mapping hydration water molecules in the HIV-1 protease/DMP323 complex in solution by NMR spectroscopy. | Q36823608 | ||
Fluorescence quenching studies with proteins | Q40319392 | ||
Structure-based inhibitors of HIV-1 protease | Q40835286 | ||
1La and 1Lb transitions of tryptophan: applications of theory and experimental observations to fluorescence of proteins | Q41487320 | ||
HIV-protease inhibitors | Q41751665 | ||
Tryptophan dynamics of the FK506 binding protein: time-resolved fluorescence and simulations | Q42184486 | ||
Secondary structure and signal assignments of human-immunodeficiency-virus-1 protease complexed to a novel, structure-based inhibitor | Q42612484 | ||
Solution NMR evidence that the HIV-1 protease catalytic aspartyl groups have different ionization states in the complex formed with the asymmetric drug KNI-272. | Q43452863 | ||
Resolution of the fluorescence excitation spectrum of indole into the 1La and 1Lb excitation bands | Q43613421 | ||
Determination of kinetic rate constants for the binding of inhibitors to HIV-1 protease and for the association and dissociation of active homodimer | Q44660459 | ||
Flexibility and function in HIV-1 protease | Q44801403 | ||
Substrate-dependent mechanisms in the catalysis of human immunodeficiency virus protease | Q45780866 | ||
Effect of pH and nonphysiological salt concentrations on human immunodeficiency virus-1 protease dimerization | Q45784308 | ||
Regulation of autoproteolysis of the HIV-1 and HIV-2 proteases with engineered amino acid substitutions | Q46436480 | ||
Microperoxidase-11: molecular dynamics and Q-band excited resonance Raman of the oxidized, reduced and carbonyl forms. | Q47821451 | ||
Toward understanding tryptophan fluorescence in proteins | Q47839130 | ||
Time resolved fluorescence and phosphorescence properties of the individual tryptophan residues of barnase: evidence for protein-protein interactions. | Q50518253 | ||
Electrostatic effects in proteins: comparison of dielectric and charge models | Q52422371 | ||
Flap opening in HIV-1 protease simulated by 'activated' molecular dynamics. | Q53849991 | ||
Backbone dynamics of Tet repressor alpha8intersectionalpha9 loop. | Q54060204 | ||
The HIV-1 protease as enzyme and substrate: mutagenesis of autolysis sites and generation of a stable mutant with retained kinetic properties. | Q54197412 | ||
Quenching of tryptophan fluorescence by the active-site disulfide bridge in the DsbA protein from Escherichia coli. | Q54565539 | ||
Correlation of tryptophan fluorescence intensity decay parameters with proton NMR-determined rotamer conformations: [tryptophan2]oxytocin | Q67748090 | ||
P433 | issue | 11 | |
P921 | main subject | rotamer | Q67936600 |
P304 | page(s) | 2232-2245 | |
P577 | publication date | 2000-11-01 | |
P1433 | published in | Protein Science | Q7251445 |
P1476 | title | Trp42 rotamers report reduced flexibility when the inhibitor acetyl-pepstatin is bound to HIV-1 protease | |
P478 | volume | 9 |
Q33968760 | Co-lethality studied as an asset against viral drug escape: the HIV protease case |
Q42952886 | Insights into Intramolecular Trp and His Side‐Chain Orientation and Stereospecific π Interactions Surrounding Metal Centers: An Investigation Using Protein Metal‐Site Mimicry in Solution |
Q44535556 | Regulation of ACTH levels in anterior pituitary cells during stimulated secretion: evidence for aspartyl and cysteine proteases in the cellular metabolism of ACTH. |
Q34403331 | The analysis of time resolved protein fluorescence in multi-tryptophan proteins |
Search more.