Disease-causing Mutations in the Cellular Retinaldehyde Binding Protein Tighten and Abolish Ligand Interactions
Open Access
- 1 April 2003
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 278 (14) , 12397-12402
- https://doi.org/10.1074/jbc.m207300200
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Mapping the Ligand Binding Pocket in the Cellular Retinaldehyde Binding ProteinJournal of Biological Chemistry, 2003
- Newfoundland Rod-Cone Dystrophy, an Early-Onset Retinal Dystrophy, Is Caused by Splice-Junction Mutations in RLBP1American Journal of Human Genetics, 2002
- Fundus albipunctatus and retinitis punctata albescens in a pedigree with an R150Q mutation in RLBP1Clinical Genetics, 2001
- Localization of the RAR interaction domain of cellular retinoic acid binding protein-IIJournal of Molecular Biology, 2001
- Amino Acid AnalysisCurrent Protocols in Protein Science, 1997
- Retinoids and the Visual ProcessPhotochemistry and Photobiology, 1996
- NMRPipe: A multidimensional spectral processing system based on UNIX pipesJournal of Biomolecular NMR, 1995
- Control of substrate flow at a branch in the visual cycleBiochemistry, 1994
- A common sense approach to peak picking in two-, three-, and four-dimensional spectra using automatic computer analysis of contour diagramsJournal of Magnetic Resonance (1969), 1991
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976