2KVC

Solution structure of the Mycobacterium tuberculosis protein Rv0543c, a member of the DUF3349 superfamily. Seattle Structural Genomics Center for Infectious Disease target MytuD.17112.a

2KVC の概要

• エントリーDOI: 10.2210/pdb2kvc/pdb
• NMR情報: BMRB: 16774
• 分子名称: Putative uncharacterized protein (1 entity in total)
• 機能のキーワード: tuberculosis, structural genomics, seattle structural genomics center for infectious disease, ssgcid, unknown function
• 由来する生物種: Mycobacterium tuberculosis
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 11608.07

構造登録者

Buchko, G.W.,Kim, C.Y.,Terwilliger, T.C.,Seattle Structural Genomics Center for Infectious Disease (SSGCID) (登録日: 2010-03-12, 公開日: 2010-03-23, 最終更新日: 2024-05-01)

主引用文献

Buchko, G.W.,Phan, I.,Myler, P.J.,Terwilliger, T.C.,Kim, C.Y.
Inaugural structure from the DUF3349 superfamily of proteins, Mycobacterium tuberculosis Rv0543c.
Arch.Biochem.Biophys., 506:150-156, 2011

PubMed Abstract: The first structure for a member of the DUF3349 (PF11829) family of proteins, Rv0543c from Mycobacterium tuberculosis, has been determined using NMR-based methods and some of its biophysical properties characterized. Rv0543c is a 100 residue, 11.3 kDa protein that both size exclusion chromatography and NMR spectroscopy show to be a monomer in solution. The structure of the protein consists of a bundle of five α-helices, α1 (M1-Y16), α2 (P21-C33), α3 (S37-G52), α4 (G58-H65) and α5 (S72-G87), held together by a largely conserved group of hydrophobic amino acid side chains. Heteronuclear steady-state {¹H}-¹⁵N NOE, T₁, and T₂ values are similar through-out the sequence indicating that the backbones of the five helices are in a single motional regime. The thermal stability of Rv0543c, characterized by circular dichroism spectroscopy, indicates that Rv0543c irreversibly unfolds upon heating with an estimated melting temperature of 62.5 °C. While the biological function of Rv0543c is still unknown, the presence of DUF3349 proteins predominantly in Mycobacterium and Rhodococcus bacterial species suggests that Rv0543 may have a biological function unique to these bacteria, and consequently, may prove to be an attractive drug target to combat tuberculosis.

PubMed: 21144816
DOI: 10.1016/j.abb.2010.12.001

実験手法

SOLUTION NMR