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Human aminolevulinate synthase structure reveals a eukaryotic-specific autoinhibitory loop regulating substrate binding and product release

Author

Listed:
  • Henry J. Bailey

    (Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford)

  • Gustavo A. Bezerra

    (Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford)

  • Jason R. Marcero

    (Department of Biochemistry and Molecular Biology, University of Georgia)

  • Siladitya Padhi

    (TCS Innovation Labs-Hyderabad (Life Sciences Division), Tata Consultancy Services Ltd)

  • William R. Foster

    (Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford)

  • Elzbieta Rembeza

    (Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford)

  • Arijit Roy

    (TCS Innovation Labs-Hyderabad (Life Sciences Division), Tata Consultancy Services Ltd)

  • David F. Bishop

    (Department of Genetics and Genomics Sciences, Icahn School of Medicine at Mount Sinai)

  • Robert J. Desnick

    (Department of Genetics and Genomics Sciences, Icahn School of Medicine at Mount Sinai)

  • Gopalakrishnan Bulusu

    (TCS Innovation Labs-Hyderabad (Life Sciences Division), Tata Consultancy Services Ltd)

  • Harry A. Dailey

    (Department of Biochemistry and Molecular Biology, University of Georgia)

  • Wyatt W. Yue

    (Structural Genomics Consortium, Nuffield Department of Medicine, University of Oxford)

Abstract

5′-aminolevulinate synthase (ALAS) catalyzes the first step in heme biosynthesis, generating 5′-aminolevulinate from glycine and succinyl-CoA. Inherited frameshift indel mutations of human erythroid-specific isozyme ALAS2, within a C-terminal (Ct) extension of its catalytic core that is only present in higher eukaryotes, lead to gain-of-function X-linked protoporphyria (XLP). Here, we report the human ALAS2 crystal structure, revealing that its Ct-extension folds onto the catalytic core, sits atop the active site, and precludes binding of substrate succinyl-CoA. The Ct-extension is therefore an autoinhibitory element that must re-orient during catalysis, as supported by molecular dynamics simulations. Our data explain how Ct deletions in XLP alleviate autoinhibition and increase enzyme activity. Crystallography-based fragment screening reveals a binding hotspot around the Ct-extension, where fragments interfere with the Ct conformational dynamics and inhibit ALAS2 activity. These fragments represent a starting point to develop ALAS2 inhibitors as substrate reduction therapy for porphyria disorders that accumulate toxic heme intermediates.

Suggested Citation

  • Henry J. Bailey & Gustavo A. Bezerra & Jason R. Marcero & Siladitya Padhi & William R. Foster & Elzbieta Rembeza & Arijit Roy & David F. Bishop & Robert J. Desnick & Gopalakrishnan Bulusu & Harry A. D, 2020. "Human aminolevulinate synthase structure reveals a eukaryotic-specific autoinhibitory loop regulating substrate binding and product release," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16586-x
    DOI: 10.1038/s41467-020-16586-x
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    Cited by:

    1. Deborah E. Daniels & Ivan Ferrer-Vicens & Joseph Hawksworth & Tatyana N. Andrienko & Elizabeth M. Finnie & Natalie S. Bretherton & Daniel C. J. Ferguson & A. Sofia. F. Oliveira & Jenn-Yeu A. Szeto & M, 2023. "Human cellular model systems of β-thalassemia enable in-depth analysis of disease phenotype," Nature Communications, Nature, vol. 14(1), pages 1-14, December.

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