Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.11.13 (
protein kinase C
)
49,245
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The cell wall integrity signaling (CWIS) pathway is involved in fungal cell wall biogenesis. This pathway is composed of sensor proteins,
protein kinase C
(
PKC
), and the mitogen-activated protein kinase (MAPK) pathway, and it controls the transcription of many cell wall-related genes.
PKC
plays a pivotal role in this pathway; deficiencies in PkcA in the model filamentous fungus
Aspergillus nidulans
and in MgPkc1p in the rice blast fungus
Magnaporthe grisea
are lethal. This suggests that
PKC
in filamentous fungi is a potential target for antifungal agents. In the present study, to search for MgPkc1p inhibitors, we carried out
in silico
screening by three-dimensional (3D) structural modeling and performed growth inhibition tests for
M. grisea
on agar plates. From approximately 800,000 candidate compounds, we selected Z-705 and evaluated its inhibitory activity against chimeric
PKC
expressed in
Saccharomyces cerevisiae
cells in which the kinase domain of native
S. cerevisiae
PKC
was replaced with those of PKCs of filamentous fungi. Transcriptional analysis of
MLP1
, which encodes a downstream factor of
PKC
in
S. cerevisiae
, and phosphorylation analysis of the mitogen-activated protein kinase (MAPK) Mpk1p, which is activated downstream of
PKC
, revealed that Z-705 specifically inhibited PKCs of filamentous fungi. Moreover, the inhibitory activity of Z-705 was similar to that of a well-known
PKC
inhibitor, staurosporine. Interestingly, Z-705 inhibited melanization induced by cell wall stress in
M. grisea
We discuss the relationships between
PKC
and melanin biosynthesis.
IMPORTANCE
A candidate inhibitor of filamentous fungal
protein kinase C
(
PKC
), Z-705, was identified by
in silico
screening. A screening system to evaluate the effects of fungal
PKC
inhibitors was constructed in
Saccharomyces cerevisiae
Using this system, we found that Z-705 is highly selective for filamentous fungal
PKC
in comparison with
S. cerevisiae
PKC
. Analysis of the
AGS1
mRNA level, which is regulated by Mps1p mitogen-activated protein kinase (MAPK) via
PKC
, in the rice blast fungus
Magnaporthe grisea
revealed that Z-705 had a
PKC
inhibitory effect comparable to that of staurosporine.
Micafungin
induced hyphal melanization in
M. grisea
, and this melanization, which is required for pathogenicity of
M. grisea
, was inhibited by
PKC
inhibition by both Z-705 and staurosporine. The mRNA levels of
4HNR
,
3HNR
, and
SCD1
, which are essential for melanization in
M. grisea
, were suppressed by both
PKC
inhibitors.
...
PMID:Novel Antifungal Compound Z-705 Specifically Inhibits Protein Kinase C of Filamentous Fungi. 3090 53