A paradigm for drug discovery using a conformation from the crystal structure of a presentation scaffold
- 1 December 1995
- journal article
- research article
- Published by Springer Nature in Nature Structural & Molecular Biology
- Vol. 2 (12) , 1131-1137
- https://doi.org/10.1038/nsb1295-1131
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Solvent content of protein crystalsPublished by Elsevier ,2006
- Destabilizing loop swaps in the CDRs of an immunoglobulin VL domainProtein Science, 1995
- Crystal structure of the tenth type III cell adhesion module of human fibronectinJournal of Molecular Biology, 1994
- Presentation of a Viral T Cell Epitope Expressed in the CDR3 Region of a Self Immunoglobulin MoleculeScience, 1993
- Structure of a Fibronectin Type III Domain from Tenascin Phased by MAD Analysis of the Selenomethionyl ProteinScience, 1992
- Discovering peptide ligands using epitope librariesTrends in Biochemical Sciences, 1992
- Insertion of an elastase-binding loop into interleukin-1βProtein Engineering, Design and Selection, 1991
- Learning from the immune system: laboratory methods for creating and refining molecular diversity in polypeptidesProtein Engineering, Design and Selection, 1991
- The Growth and Preliminary Investigation of Protein and Nucleic Acid Crystals for X‐ray Diffraction AnalysisPublished by Wiley ,1976
- Crystal and Molecular Structure of a Dimer Composed of the Variable Portions of the Bence-Jones Protein REIEuropean Journal of Biochemistry, 1974