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© Institut Pasteur
Cells infected for 24 hrs with C. Trachomatis. The cell nuclei are labelled in blue, the bacteria appear yellow, within the inclusion lumen. A bacterial protein secreted out the inclusion into the host cytoplasm id labelled in red.
Publication : Acta crystallographica Section D : Structural biology [1993-...]

Insights into the inter-ring plasticity of caseinolytic proteases from the X-ray structure of Mycobacterium tuberculosis ClpP1.

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Acta crystallographica Section D : Structural biology [1993-...] - 01 Feb 2007

Henrik Ingvarsson, María J. Maté, Martin Högbom, Denis Portnoï, Nadia Benaroudj, Pedro Maria Alzari, Miguel Ortiz-Lombardía, Torsten Unge

Link to Pubmed [PMID] – 17242518

Link to HAL – hal-00167558

Link to DOI – 10.1107/S0907444906050530

Acta crystallographica Section D : Structural biology [1993-..], 2007, 63 (Pt 2), pp.249-59. ⟨10.1107/S0907444906050530⟩

Mycobacterium tuberculosis caseinolytic protease ClpP1 (Mt ClpP1) is a self-compartmentalized protease consisting of two heptameric rings stacked on top of each other, thus enclosing a catalytic chamber. Within the chamber, which can be reached through two axial pores, each of the 14 identical monomers possesses a serine protease active site. The unfolding and translocation of substrates into the chamber are mediated by associated hexameric ATPases covering the axial pores. Three crystal structures of Mt ClpP1, determined by molecular replacement, are presented in this study. Two of the models were refined to a resolution of 2.6 A and the third to 3.0 A. It was found that disorder in the handle domain affects the formation and configuration of the tetradecamer and results in condensed structures with larger equatorial pores when compared with ClpPs from other species. Additionally, this disorder accompanies conformational changes of the residues in the catalytic triad. The models also reveal structural differences within the N-terminal hairpin-loop domain, which possibly reflect the significant differences in amino-acid sequence between Mt ClpP1 and other ClpP homologues in this region.