Fig. 3: Conformational flexibility of M. tuberculosis RNAP. | Nature Communications

Fig. 3: Conformational flexibility of M. tuberculosis RNAP.

From: Structural basis of the mycobacterial stress-response RNA polymerase auto-inhibition via oligomerization

Fig. 3

Motions of the RNAP flap (a) and clamp (b). RNAP is shown as a molecular surface with the core subunits in gray and σB in yellow. The flap (β flap, β subunit aa 808–832) and clamp (β‘ subunit aa 1–413, 1219–1245; β subunit aa 1117–1140) domains are shown as cartoons with cylindrical helices. Rotation angles were measured in PyMol as described by26. a The β flap position in EσB (in red) relative to its position in RbpA/σA-RPo (blue, PDB ID 6C04) and in the T. thermophilus gp39/EσA complex (pink, PDB ID 3WOD). b The clamp position in EσB (in red) relative to RbpA/σA-RPo (blue, PDB ID 6C04) and RbpA/EσA (orange, PDB ID 6C05). c Comparison of the σB and σA (PDB ID 6C05) structures. The σ subunits are shown as ribbons with domain σ1.1 in white, subregion R1.2 in red, NCR in yellow, R2 in goldenrod. d Motions of domain σ1.1. Superposition of σ1.1 in EσB (dark red), RbpA/EσA (light blue) and RbpA/CarD/EσA (green, PDB ID 6EDT). The RNAP core is shown as a molecular surface in gray. σA and σB are shown as ribbons; dwDNA (blue): downstream fragment of promoter DNA duplex.

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