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Three-dimensional NMR structure of the sixth ligand-binding module of the human LDL receptor: comparison of two adjacent modules with different ligand binding specificities
- Source :
- FEBS Letters. 479:118-122
- Publication Year :
- 2000
- Publisher :
- Wiley, 2000.
-
Abstract
- The sixth ligand-binding module of the low-density lipoprotein receptor contributes to the binding of apolipoprotein B100-containing lipoproteins. 1H NMR spectroscopy, DYANA and X-PLOR structure calculations were used to determine that this module has a well defined structure with a backbone conformation similar to other modules. Structures from calculations that simulated the presence of a calcium ion showed increased resolution without large increases in energy, increased deviations from idealised geometry or violations of experimental constraints. Investigation of the surface properties of this module indicates there are significant differences from the fifth module, which binds apolipoprotein E-containing lipoproteins in addition to apolipoprotein B100-containing lipoproteins.
- Subjects :
- Models, Molecular
Magnetic Resonance Spectroscopy
Apolipoprotein B
Molecular Sequence Data
Biophysics
Plasma protein binding
Ligands
Biochemistry
Protein Structure, Secondary
Protein structure
Structural Biology
Genetics
Humans
Amino Acid Sequence
Binding site
Molecular Biology
Peptide sequence
Ions
Binding Sites
Sequence Homology, Amino Acid
biology
Chemistry
Cell Biology
Nuclear magnetic resonance spectroscopy
Protein Structure, Tertiary
Crystallography
Models, Chemical
Receptors, LDL
LDL receptor
biology.protein
Calcium
lipids (amino acids, peptides, and proteins)
Algorithms
Protein Binding
Lipoprotein
Subjects
Details
- ISSN :
- 00145793
- Volume :
- 479
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....41808f01f4547690f21ca13dfec01e08
- Full Text :
- https://doi.org/10.1016/s0014-5793(00)01842-1