Abstract

Filamentation induced by cAMP (Fic) domain proteins have been shown to catalyze the transfer of the AMP moiety from ATP onto a protein target. This type of post-translational modification was recently shown to play a crucial role in pathogenicity mediated by two bacterial virulence factors. Herein we characterize a novel Fic domain protein that we identified from the human pathogen Clostridium difficile The crystal structure shows that the protein adopts a classical all-helical Fic fold, which belongs to class II of Fic domain proteins characterized by an intrinsic N-terminal autoinhibitory α-helix. A conserved glutamate residue in the inhibitory helix motif was previously shown in other Fic domain proteins to prevent proper binding of the ATP γ-phosphate. However, here we demonstrate that both ATP binding and autoadenylylation activity of the C. difficile Fic domain protein are independent of the inhibitory motif. In support of this, the crystal structure of a mutant of this Fic protein in complex with ATP reveals that the γ-phosphate adopts a conformation unique among Fic domains that seems to override the effect of the inhibitory helix. These results provide important structural insight into the adenylylation reaction mechanism catalyzed by Fic domains. Our findings reveal the presence of a class II Fic domain protein in the human pathogen C. difficile that is not regulated by autoinhibition and challenge the current dogma that all class I-III Fic domain proteins are inhibited by the inhibitory α-helix.

Highlights

  • Clostridium difficile is a Gram-positive, anaerobic, and spore-forming pathogen recognized as the leading cause of healthcare-associated diarrhea [1,2,3]

  • Here we demonstrate that both ATP binding and autoadenylylation activity of the C. difficile filamentation induced by cAMP (Fic) domain protein are independent of the inhibitory motif

  • This is the first Fic domain protein identified with autoadenylylation activity incompatible with the proposed

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Summary

The abbreviations used are

Filamentation induced by cAMP; ␣inh, inhibitory ␣-helix; HYPE, huntingtin yeast interacting protein E; AU, asymmetric unit; SEC, size exclusion chromatography; DSF, differential scanning fluorimetry; EOM, ensemble optimization method; SAXS, small angle x-ray scattering; SE/AA, S31A/Einh35A; Cd, C. difficile; Nm, N. meningitides; Bt, B. thetaiotaomicron; Hp, H. pylori. It was shown that adenylylation activity of some Fic domains is controlled by a conserved mechanism of ATP binding site obstruction involving an intrinsic inhibitory ␣-helix (␣inh) containing a conserved (S/T)XXXEinh(G/N) inhibitory motif [21]. The conserved glutamate in this inhibitory motif, Gluinh, has been found to cause a steric hindrance of proper positioning of the ATP ␥-phosphate [21, 28] This autoinhibition was further supported by substitutions of Gluinh with either alanine or glycine, which resulted in increased levels of autoadenylylation as well as target adenylylation in vitro [15, 16, 21, 28]. The overall structural fold is similar to other Fic domains, we show that CdFic binds ATP as well as catalyzes autoadenylylation independently of the inhibitory motif

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