Flt3 ligand structure and unexpected commonalities of helical bundles and cystine knots.

Program in Biophysics, Cornell University, Ithaca, NY 14853, USA.
Human Flt3 ligand (Flt3L) stimulates early hematopoiesis by activating a type III tyrosine kinase receptor on primitive bone marrow stem cells. The crystal structure of soluble Flt3L reveals that it is a homodimer of two short chain alpha-helical bundles. Comparisons of structure-function relationships of Flt3L with the homologous hematopoietic cytokines macrophage colony stimulating factor (MCSF) and stem cell factor (SCF) suggest that they have a common receptor binding mode that is distinct from the paradigm derived from the complex of growth hormone with its receptor. Furthermore, we identify recognition features common to all helical and cystine-knot protein ligands that activate type III tyrosine kinase receptors, and the closely related type V tyrosine kinase receptors.
Mesh Terms:
Amino Acid Sequence, Binding Sites, Consensus Sequence, Crystallography, X-Ray, Cystine, Dimerization, Humans, Ligands, Macrophage Colony-Stimulating Factor, Membrane Proteins, Models, Molecular, Molecular Sequence Data, Mutation, Peptide Fragments, Protein Structure, Secondary, Protein Structure, Tertiary, Proto-Oncogene Proteins, Receptor Protein-Tyrosine Kinases, Receptors, Platelet-Derived Growth Factor, Sequence Alignment, Stem Cell Factor, Structure-Activity Relationship, fms-Like Tyrosine Kinase 3
Nat. Struct. Biol. Jun. 01, 2000; 7(6);486-91 [PUBMED:10881197]
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