Identification of Ser/Thr kinase and forkhead associated domains in Mycobacterium ulcerans: characterization of novel association between protein kinase Q and MupFHA

• Published in: PLoS neglected tropical diseases 2014-11, Vol.8 (11), p.e3315-e3315
• Main Authors: Arora, Gunjan, Sajid, Andaleeb, Singhal, Anshika, Joshi, Jayadev, Virmani, Richa, Gupta, Meetu, Verma, Nupur, Maji, Abhijit, Misra, Richa, Baronian, Grégory, Pandey, Amit K, Molle, Virginie, Singh, Yogendra
• Format: Article
• Language: English
• Subjects: Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; Bacteriology; Binding sites; Biology and Life Sciences; Buruli ulcer; Cell division; Cloning; Computational Biology; Drug resistance; Forkhead Transcription Factors - chemistry; Forkhead Transcription Factors - metabolism; Genetic aspects; Kinases; Life Sciences; Medicine and Health Sciences; Microbiological research; Microbiology and Parasitology; Molecular Dynamics Simulation; Mycobacteria; Mycobacterium; Mycobacterium marinum; Mycobacterium tuberculosis; Mycobacterium ulcerans; Mycobacterium ulcerans - chemistry; Mycobacterium ulcerans - enzymology; Mycobacterium ulcerans - metabolism; Pathogenesis; Peptides; Phosphatase; Phosphorylation; Protein Binding; Protein kinases; Protein Structure, Tertiary; Protein-Serine-Threonine Kinases - chemistry; Protein-Serine-Threonine Kinases - metabolism; Proteins; Studies; Tuberculosis; Ulcers
• ISSN: 1935-2735; 1935-2727; 1935-2735
• DOI: 10.1371/journal.pntd.0003315

Mycobacterium ulcerans, the causative agent of Buruli ulcer in humans, is unique among the members of Mycobacterium genus due to the presence of the virulence determinant megaplasmid pMUM001. This plasmid encodes multiple virulence-associated genes, including mup011, which is an uncharacterized Ser/Thr protein kinase (STPK) PknQ. In this study, we have characterized PknQ and explored its interaction with MupFHA (Mup018c), a FHA domain containing protein also encoded by pMUM001. MupFHA was found to interact with PknQ and suppress its autophosphorylation. Subsequent protein-protein docking and molecular dynamic simulation analyses showed that this interaction involves the FHA domain of MupFHA and PknQ activation loop residues Ser170 and Thr174. FHA domains are known to recognize phosphothreonine residues, and therefore, MupFHA may be acting as one of the few unusual FHA-domain having overlapping specificity. Additionally, we elucidated the PknQ-dependent regulation of MupDivIVA (Mup012c), which is a DivIVA domain containing protein encoded by pMUM001. MupDivIVA interacts with MupFHA and this interaction may also involve phospho-threonine/serine residues of MupDivIVA. Together, these results describe novel signaling mechanisms in M. ulcerans and show a three-way regulation of PknQ, MupFHA, and MupDivIVA. FHA domains have been considered to be only pThr specific and our results indicate a novel mechanism of pSer as well as pThr interaction exhibited by MupFHA. These results signify the need of further re-evaluating the FHA domain -pThr/pSer interaction model. MupFHA may serve as the ideal candidate for structural studies on this unique class of modular enzymes.