A) NO activates guanylyl cyclase,which catalyzes the synthesis of cGMP,which acts as an intracellular messenger in a pathway leading to smooth muscle relaxation.
B) NO activates a protein kinase which catalyzes the synthesis of cGMP,which acts as an intracellular messenger in a pathway leading to smooth muscle relaxation.
C) NO inhibits guanylyl cyclase,which allows the build up of cGMP,which acts as an intracellular messenger in a pathway leading to smooth muscle relaxation.
D) NO activates cGMP,which catalyzes the synthesis of guanylyl cyclase,which acts as an intracellular messenger in a pathway leading to smooth muscle relaxation.
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Multiple Choice
A) The substrate will be phosphorylated normally in the presence of molecule X.
B) Less phosphorylation of the substrate will be seen in the presence of molecule X.
C) More phosphorylation of the substrate will be seen in the presence of molecule X.
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Multiple Choice
A) catalyze the conversion of ATP to cAMP.
B) cleave PIP2 into DAG and IP3.
C) directly activate protein kinase A (PKA) .
D) stimulate the release of calcium from the endoplasmic reticulum.
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Multiple Choice
A) chemical synapse.
B) neuron junction.
C) paracrine space.
D) gap junction.
E) plasmodesmata.
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Multiple Choice
A) GTP is not required for phosphorylation.
B) The substrate can undergo autophosphorylation.
C) The substrate is not required for phosphorylation.
D) The protein kinase is required for phosphorylation.
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Multiple Choice
A) MAP kinase
B) MAP kinase kinase
C) MAP kinase kinase kinase
D) MAP phosphatase
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Multiple Choice
A) Direct contact
B) Paracrine
C) Endocrine
D) Synaptic
E) Autocrine
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Multiple Choice
A) A protein kinase
B) A receptor tyrosine kinase
C) A G protein-coupled receptor
D) A tyrosine phosphatase
E) A phospholipase
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Multiple Choice
A) Direct contact
B) Paracrine
C) Endocrine
D) Synaptic
E) Autocrine
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Multiple Choice
A) signal amplification.
B) signal transduction.
C) signal dampening.
D) signal activation.
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Multiple Choice
A) Scaffold
B) Adapter protein
C) Second messenger
D) Enzyme
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Multiple Choice
A) Channel-linked receptor
B) Enzymatic receptor
C) G protein-coupled receptor
D) Steroid hormone receptor
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Multiple Choice
A) Channel-linked receptor
B) Enzymatic receptor
C) G protein-coupled receptor
D) Steroid hormone receptor
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Multiple Choice
A) The plasma membrane fraction
B) The extracellular fraction
C) The cytoplasmic fraction
D) The mitochondrial fraction
E) The ribosomal fraction
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Multiple Choice
A) DAG
B) cAMP
C) cGMP
D) Phospholipase C
E) G protein
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Multiple Choice
A) GTP would remain bound to Ras,thereby keeping Ras constitutively active.
B) GDP would remain bound to Ras,thereby preventing Ras activation.
C) Ras would be more likely to hydrolyze GTP to GDP.
D) There would be no effect.
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Multiple Choice
A) genes.
B) intracellular receptors.
C) second messengers.
D) first messengers.
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Multiple Choice
A) Ras is an enzyme and the G proteins bound to GPCRs are not enzymes.
B) Ras is a second messenger and the G proteins bound to GPCRs are not second messengers.
C) Ras is a small G protein and the G proteins bound to GPCRs are not small G proteins.
D) Ras can activate different effector molecules and the G proteins bound to GPCRs cannot activate different effector molecules.
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Multiple Choice
A) Phosphate groups are efficient second messengers
B) Protein kinases and phosphatases are abundant in most cells
C) The hydrolysis of bound GTP generates GDP,which can change the activity of proteins bound to GDP
D) The addition or removal of a phosphate group can expose or hide potential binding sites in proteins or change protein activity
Correct Answer
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Multiple Choice
A) Tamoxifen binds different parts of the estrogen receptor in different tissues.
B) The estrogen receptor is bound to different coactivators in different tissues.
C) Tamoxifen can only enter certain cell types.
D) Bone cells make use of a different type of estrogen receptor that does not bind to Tamoxifen.
Correct Answer
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