X-Ray Structures and Analysis of 11 Cyclosporin Derivatives Complexed with Cyclophilin A.
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Summary
Eight new X-ray structures of different cyclophilin A/cyclosporin-derivative complexes are presented and provide a useful structural database for the analysis of protein-ligand interactions.
- Type
- article
- Published
- 1998-10-01
- Cited by
- 69
- References
- 49
- OpenAlex
- https://openalex.org/W9769216
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:29912825
Keywords
Medicine
References
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- LUDI: rule-based automatic design of new substituents for enzyme inhibitor leads
- Similarities and differences between human cyclophilin A and other beta-barrel structures. Structural refinement at 1.63 A resolution.
- The development of a simple empirical scoring function to estimate the binding constant for a protein-ligand complex of known three-dimensional structure
- Determination of the NMR solution structure of the cyclophilin A-cyclosporin A complex
- Modification of Cyclosporin A (CS): Generation of an enolate at the sarcosine residue and reactions with electrophiles
- Hydrogen bonding in globular proteins.
- Cyclosporine and analogues: structural requirements for immunosuppressive activity.
- Crystallization of the complex between cyclophilin A and cyclosporin derivatives: the use of cross-seeding.
- Crystal structures of human calcineurin and the human FKBP12–FK506–calcineurin complex
- Peptidylproline cis-trans-isomerases: immunophilins.
- Conformation of cyclosporin A in polar solvents.
- Peptide conformations. Part 31. The conformation of cyclosporin a in the crystal and in solution
- The X‐ray structure of a tetrapeptide bound to the active site of human cyclophilin A
- Energetic origins of specificity of ligand binding in an interior nonpolar cavity of T4 lysozyme.
- Crystal orientation and X-ray pattern prediction routines for area-detector diffractometer systems in macromolecular crystallography
- The role of water molecules in the structure-based design of (5-hydroxynorvaline)-2-cyclosporin: synthesis, biological activity, and crystallographic analysis with cyclophilin A.
- A Kinetic Analysis of the Folding of Human Carbonic Anhydrase II and Its Catalysis by Cyclophilin (*)
- Is cyclophilin involved in the immunosuppressive and nephrotoxic mechanism of action of cyclosporin A?
Cited by
- X-ray structure of alisporivir in complex with cyclophilin A at 1.5 Å resolution.
- Using Molecular Dynamics to Elucidate the Mechanism of Cyclophilin
- Probing protein-ligand interactions via solution phase hydrogen exchange mass spectrometry
- Effects of ligand binding on the rigidity and mobility of proteins : a computational and experimental approach
- Two structures of cyclophilin 40: folding and fidelity in the TPR domains.
- Synthesis and characterization of constrained cyclosporin A derivatives containing a pseudo-proline group
- Exo‐Mechanism Proximity‐Accelerated Alkylations: Investigations of Linkers, Electrophiles and Surface Mutations in Engineered Cyclophilin–Cyclosporin Systems
- Two new cyclosporin folds observed in the structures of the immunosuppressant cyclosporin G and the formyl peptide receptor antagonist cyclosporin H at ultra-high resolution.
- Immunophilins and HIV-1 V3 Loop For Structure-Based Anti-AIDS Drug Design
- Thermodynamics of the cyclophilin-A/cyclosporin-A interaction: a direct comparison of parameters determined by surface plasmon resonance using Biacore T100 and isothermal titration calorimetry.
- Structure of a bacterial cytoplasmic cyclophilin A in complex with a tetrapeptide.
- Equilibrium unfolding of cyclophilin from Leishmania donovani: characterization of intermediate states.
- Immunophilins: Switched on protein binding domains?
- 1.88 A crystal structure of the C domain of hCyP33: a novel domain of peptidyl-prolyl cis-trans isomerase.
- Computational Model of the HIV-1 Subtype A V3 Loop: Study on the Conformational Mobility for Structure-Based Anti-AIDS Drug Design
- The three-dimensional structure of a Plasmodium falciparum cyclophilin in complex with the potent anti-malarial cyclosporin A.
- Structural and Biochemical Characterization of the Human Cyclophilin Family of Peptidyl-Prolyl Isomerases
- Preparation, Characterization and Refolding in Vitro of a Recombinant Human Cyclophilin A Mutant: Effect of a Single Pro/Ser Substitution on Cyclophilin A Structure and Properties
- Structural basis for the non-immunosuppressive character of the cyclosporin A analogue Debio 025.
- Enzymatic and structural characterization of non-peptide ligand-cyclophilin complexes.
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