6VSX

X-ray crystal structure of the C-terminal domain of Bacillus subtilis RNA polymerase binding helicase HelD


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.00 Å
  • R-Value Free: 0.202 
  • R-Value Work: 0.172 
  • R-Value Observed: 0.175 

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This is version 1.2 of the entry. See complete history


Literature

Mycobacterial HelD is a nucleic acids-clearing factor for RNA polymerase.

Kouba, T.Koval', T.Sudzinova, P.Pospisil, J.Brezovska, B.Hnilicova, J.Sanderova, H.Janouskova, M.Sikova, M.Halada, P.Sykora, M.Barvik, I.Novacek, J.Trundova, M.Duskova, J.Skalova, T.Chon, U.Murakami, K.S.Dohnalek, J.Krasny, L.

(2020) Nat Commun 11: 6419-6419

  • DOI: https://doi.org/10.1038/s41467-020-20158-4
  • Primary Citation of Related Structures:  
    6VSX, 6YXU, 6YYS

  • PubMed Abstract: 

    RNA synthesis is central to life, and RNA polymerase (RNAP) depends on accessory factors for recovery from stalled states and adaptation to environmental changes. Here, we investigated the mechanism by which a helicase-like factor HelD recycles RNAP. We report a cryo-EM structure of a complex between the Mycobacterium smegmatis RNAP and HelD. The crescent-shaped HelD simultaneously penetrates deep into two RNAP channels that are responsible for nucleic acids binding and substrate delivery to the active site, thereby locking RNAP in an inactive state. We show that HelD prevents non-specific interactions between RNAP and DNA and dissociates stalled transcription elongation complexes. The liberated RNAP can either stay dormant, sequestered by HelD, or upon HelD release, restart transcription. Our results provide insights into the architecture and regulation of the highly medically-relevant mycobacterial transcription machinery and define HelD as a clearing factor that releases RNAP from nonfunctional complexes with nucleic acids.


  • Organizational Affiliation

    EMBL Grenoble, 71 Avenue des Martyrs, Grenoble, France. tkouba@embl.fr.


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
DNA helicase188Bacillus subtilisMutation(s): 0 
Gene Names: B4417_3167
EC: 3.6.4.12
UniProt
Find proteins for O32215 (Bacillus subtilis (strain 168))
Explore O32215 
Go to UniProtKB:  O32215
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupO32215
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 1 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
PO4 (Subject of Investigation/LOI)
Query on PO4

Download Ideal Coordinates CCD File 
B [auth A]PHOSPHATE ION
O4 P
NBIIXXVUZAFLBC-UHFFFAOYSA-K
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.00 Å
  • R-Value Free: 0.202 
  • R-Value Work: 0.172 
  • R-Value Observed: 0.175 
  • Space Group: C 1 2 1
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 106.963α = 90
b = 38.813β = 101.448
c = 44.427γ = 90
Software Package:
Software NamePurpose
PHENIXrefinement
HKL-2000data reduction
HKL-2000data scaling
PHENIXphasing
PHENIXmodel building

Structure Validation

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Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)United StatesGM131860

Revision History  (Full details and data files)

  • Version 1.0: 2020-06-10
    Type: Initial release
  • Version 1.1: 2021-01-13
    Changes: Database references
  • Version 1.2: 2024-03-06
    Changes: Data collection, Database references