 |
PDBsum entry 6ev0
|
|
|
|
 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
 |
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
|
|
|
|
|
|
|
|
|
|
DNA binding protein
|
PDB id
|
|
|
|
6ev0
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
References listed in PDB file
|
 |
|
Key reference
|
 |
|
Title
|
 |
Structure-Based design of inhibitors targeting prfa, The master virulence regulator of listeria monocytogenes.
|
 |
|
Authors
|
 |
M.Kulén,
M.Lindgren,
S.Hansen,
A.G.Cairns,
C.Grundström,
A.Begum,
I.Van der lingen,
K.Brännström,
M.Hall,
U.H.Sauer,
J.Johansson,
A.E.Sauer-Eriksson,
F.Almqvist.
|
 |
|
Ref.
|
 |
J Med Chem, 2018,
61,
4165-4175.
[DOI no: ]
|
 |
|
PubMed id
|
 |
|
 |
 |
|
Abstract
|
 |
|
Listeria monocytogenes is a bacterial pathogen that controls much of its
virulence through the transcriptional regulator PrfA. In this study, we describe
structure-guided design and synthesis of a set of PrfA inhibitors based on
ring-fused 2-pyridone heterocycles. Our most effective compound decreased
virulence factor expression, reduced bacterial uptake into eukaryotic cells, and
improved survival of chicken embryos infected with L. monocytogenes compared to
previously identified compounds. Crystal structures identified an intraprotein
"tunnel" as the main inhibitor binding site (AI), where the
compounds participate in an extensive hydrophobic network that restricts the
protein's ability to form functional DNA-binding helix-turn-helix (HTH) motifs.
Our studies also revealed a hitherto unsuspected structural plasticity of the
HTH motif. In conclusion, we have designed 2-pyridone analogues that function as
site-AI selective PrfA inhibitors with potent antivirulence
properties.
|
 |
|
Secondary reference #1
|
 |
|
Title
|
 |
Attenuating listeria monocytogenes virulence by targeting the regulatory protein prfa.
|
 |
|
Authors
|
 |
J.A.Good,
C.Andersson,
S.Hansen,
J.Wall,
K.S.Krishnan,
A.Begum,
C.Grundström,
M.S.Niemiec,
K.Vaitkevicius,
E.Chorell,
P.Wittung-Stafshede,
U.H.Sauer,
A.E.Sauer-Eriksson,
F.Almqvist,
J.Johansson.
|
 |
|
Ref.
|
 |
Cell Chem Biol, 2016,
23,
404-414.
[DOI no: ]
|
 |
|
PubMed id
|
 |
|
 |
 |
|
|
 |
|
|
|
|
 |