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Intracellular signal transduction
The process in which a signal is passed on to downstream
components within the cell, which become activated themselves to further propagate the signal and finally trigger a change in the function or state of the cell.
MAPK is exploited by:
Bacterial toxins. Effector proteins. One of the key causes of anthrax virulence is the production of three specific toxins, derived from three genes lethal factor LF, protective antigen PA and edema factor EF. PA which is a cellular receptor recognizes toxins. LF and EF protein binds to the PA pre pore.In the endosomal compartment the acidic pH causes conformation change that insert PA fragment and releases LF and EF into the cytoplasm. LF acts as a protease that cleaves MAP kinase (MAPK1 & MAPK2) Type III secreted protein YOPJ of Yersinia pestis
Inhibits the activation of MAPK signaling pathway by
covalently modify key serine and threonine residues of MAP kinase.
Functions as acetyl transferase (addition of acetyl CoA).
Inability of upstream kinases to transphosphorylase the downstream kinase.
Prevent MAPK-mediated cytokine transcriptional response to
Yersinia infection ii) Salmonella, AvrA
Harbor acetyl transferase activity
Inhibit MAPK4& MAPK7(c-Jun NH2-terminal kinase) signaling pathway. Prevent the transcription of prosurvival genes
New era of anti-innate immune signaling research
Mass spectrometry analysis OspF catalyzes a b elimination reaction of phosphothreonine Produces b-methyldehydroalanine Permanent inactivity of MAPK cascade Inhibit inflammatory activation.