6QKQ
NMR solution structure of LSR2-T112D binding domain.
Summary for 6QKQ
| Entry DOI | 10.2210/pdb6qkq/pdb |
| Related | 6QKP |
| NMR Information | BMRB: 34359 |
| Descriptor | Nucleoid-associated protein Lsr2 (1 entity in total) |
| Functional Keywords | tuberculosis, dna oraganisation, transcriptional regulator, pknb substrate, dna binding protein |
| Biological source | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) |
| Total number of polymer chains | 1 |
| Total formula weight | 5508.02 |
| Authors | Barthe, P.,Cohen-Gonsaud, M.,Mukamolova, G.V. (deposition date: 2019-01-30, release date: 2019-07-17, Last modification date: 2024-06-19) |
| Primary citation | Alqaseer, K.,Turapov, O.,Barthe, P.,Jagatia, H.,De Visch, A.,Roumestand, C.,Wegrzyn, M.,Bartek, I.L.,Voskuil, M.I.,O'Hare, H.M.,Ajuh, P.,Bottrill, A.R.,Witney, A.A.,Cohen-Gonsaud, M.,Waddell, S.J.,Mukamolova, G.V. Protein kinase B controls Mycobacterium tuberculosis growth via phosphorylation of the transcriptional regulator Lsr2 at threonine 112. Mol.Microbiol., 112:1847-1862, 2019 Cited by PubMed Abstract: Mycobacterium tuberculosis (Mtb) is able to persist in the body through months of multi-drug therapy. Mycobacteria possess a wide range of regulatory proteins, including the protein kinase B (PknB) which controls peptidoglycan biosynthesis during growth. Here, we observed that depletion of PknB resulted in specific transcriptional changes that are likely caused by reduced phosphorylation of the H-NS-like regulator Lsr2 at threonine 112. The activity of PknB towards this phosphosite was confirmed with purified proteins, and this site was required for adaptation of Mtb to hypoxic conditions, and growth on solid media. Like H-NS, Lsr2 binds DNA in sequence-dependent and non-specific modes. PknB phosphorylation of Lsr2 reduced DNA binding, measured by fluorescence anisotropy and electrophoretic mobility shift assays, and our NMR structure of phosphomimetic T112D Lsr2 suggests that this may be due to increased dynamics of the DNA-binding domain. Conversely, the phosphoablative T112A Lsr2 had increased binding to certain DNA sites in ChIP-sequencing, and Mtb containing this variant showed transcriptional changes that correspond with the change in DNA binding. In summary, PknB controls Mtb growth and adaptations to the changing host environment by phosphorylating the global transcriptional regulator Lsr2. PubMed: 31562654DOI: 10.1111/mmi.14398 PDB entries with the same primary citation |
| Experimental method | SOLUTION NMR |
Structure validation
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