1. signal molecule binds and activates receptor
2. GDP disassociates and GTP activates subunit and effector
hydrolysis of GTP by the subunit inactivates the subunit and causes it to disassociate from the target protein
As long as (a) and (by) subunits are free
1. cholera - bacterium produces toxin that enters intestinal cells and alters Ga subunit
2. cell is continuously active, prolonged secretion into the gut
3. cough, bacterium colonizes lung, produces pertussin toxin that enters cells and alters Ga subunit
4. prolonged, inappropriate signal that generates coughing
1. signal molecule binds to receptor and activates (a) subunit and (by) complex, ion channel opens
2. GTP -> GDP, inactive G protein causing closed ion channel
1. second messenger molecules diffuse to act on intracellular signalling proteins
1. adrenal cyclase are activated by second messenger molecules
2. cyclic shape turns it on, breaking cyclic shape turns it off
1. epinephrine acts via a GPCr that activates adenyl cyclase
yes it activates PKA that travels down a nuclear pore and activates transcription regulator
It is activated by GPCRs and helps activate PKC with inosital 1,4,5-triphosphate entering ER lumen opening Ca2+ ion channel and Ca2+ acts as a second messenger to activate PKC
1. It is a intracellular signal
2. concentrations in the cytoskeleta=on are very low compared to outside the cell
3. cytosolic Ca2+ can be rapidy increased
4. Binding of Ca2+ activates many different proteins
receptors are enzymes themselves or associated with enzymes
1. signal molecule in form of a dimer binds to RTK and stimulates the kinase activity
2. active RTK's cause the activation of downstream intracellular signaling pathways
1. the largest class of enzyme coupled receptors
2. signal proteins recruited to cytosolic tails of RTK activated other downstream signals
Ras
1. small monomeric G-protein bound to inner membrane by lipid tail
2. acts as a molecular switch
3. active when bound to GTP, turns off by hydrolyzing it to GDP
4. Sets off relay of signals
permanently activated proteins
cancer
Ras
a failure of cell commmunication