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TitleStructures of ligand-occupied beta-Klotho complexes reveal a molecular mechanism underlying endocrine FGF specificity and activity.
Journal, issue, pagesProc. Natl. Acad. Sci. U.S.A., Vol. 116, Page 7819-7824, Year 2019
Publish dateDec 20, 2018 (structure data deposition date)
AuthorsKuzina, E.S. / Ung, P.M. / Mohanty, J. / Tome, F. / Choi, J. / Pardon, E. / Steyaert, J. / Lax, I. / Schlessinger, A. / Schlessinger, J. / Lee, S.
External linksProc. Natl. Acad. Sci. U.S.A. / PubMed:30944224
MethodsX-ray diffraction
Resolution3.19 Å
Structure data

PDB-6nfj:
Structure of Beta-Klotho in Complex with FGF19 C-terminal peptide
Method: X-RAY DIFFRACTION / Resolution: 3.19 Å

Source
  • homo sapiens (human)
  • lama glama (llama)
KeywordsSIGNALING PROTEIN / Klotho / FGF19 / Nanobody / receptor tyrosine kinase / signaling

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