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Signal, reception, transduction
Signal, reception, transduction

... • The G protein can also act as a GTPase enzyme and hydrolyzes the GTP, which activated it, to GDP. • This change turns the G protein off. ...
Principles of Biochemistry
Principles of Biochemistry

... •  The mitogen-activated protein kinase (MAPK) pathways are typically comprised of a three-member protein kinase cascade. •  Specificity of MAPK responses is achieved by activation of different three-kinase modules. •  There are at least three sets of mammalian MAPK modules. –  the extracellular-sig ...
Cell-Cell Interactions (Lectures 22-23)
Cell-Cell Interactions (Lectures 22-23)

... 1.) What general forces does the extracellular matrix of cells protect against? 2.) What is the primary cell wall composed of? What type of macromolecule is this? How is it packaged and arranged in the cell wall? What molecule fills the space between this cell wall material and what type of macromol ...
adrenegics
adrenegics

... 12. Why salbutamol is a catecholamine, however it has longer half-life in the body. Why? 13. How you can switch the selectivity of adrenaline analogues toward beta2-receptors? 14. How you can identify the compounds which produce their adrenergic effect without binding to adrenergic switch? Is it thr ...
DOC
DOC

... contributions to circuit rearrangements by presynaptic terminals have remained unclear. We used hippocampal slice cultures from mice expressing spectral variants of green fluorescent protein (GFP) that are targeted to the membrane and/or synaptic vesicles in neuronal subsets to image identified pres ...
SIGNAL TRANSDUCTION PATHWAYS Outline
SIGNAL TRANSDUCTION PATHWAYS Outline

... open. Calcium ions flow out of ER. Calcium levels in cytosol increase Calcium ions activate next protein in signal pathway. ...
SIGNAL TRANSDUCTION PATHWAYS Student Version Outline
SIGNAL TRANSDUCTION PATHWAYS Student Version Outline

... Calcium ions activate next protein in signal pathway. Calcium ions flow out of ER. IP3 binds to IP3 gated calcium channel receptors in ER, causing channel to open. Calcium levels in cytosol increase ...
PPT
PPT

... Ga in the off state has GDP bound and does not activate downstream signaling molecules. When a GPCR is activated by ligand, it stimulates Ga subunits to bind GTP instead of GDP and become active, dissociating from the receptor and from the b/g subunits to activate downstream signaling factors like t ...
File 07
File 07

... recognize DNA directly but are recruited by association with sequence-specific, DNA-binding proteins. HDAC cleaves the acetyl moiety from histone tails. Thyroid hormone receptor (TR) provides an example of a DNA binding protein that switches activity by changing its associated cofactor.In the absenc ...
44. a. Classify cholinergic receptors and subtypes, agonists and
44. a. Classify cholinergic receptors and subtypes, agonists and

... In addition to binding acetylcholine, also recognize nicotine and show only a weak affinity for muscarin e. The nicotinic receptor is composed of five s ubunits, and it functions as a ligand-gated ion channel . Binding of two acet ylcholine molecules elicits a conformational change that allows the e ...
Cell signaling by chemical messengers
Cell signaling by chemical messengers

... • Free catalytic subunit of PKA goes to nucleus, phosphorylates transcription factor CREB (CRE-binding protein). ...
The Cell, 5e
The Cell, 5e

... JAK-STAT receptors: tyrosine kinase-associated • Often for cytokine signaling – more direct to nucleus • JAK = Janus kinase (just another kinase); • STAT = signal transducer, activator of transcription ...
ch15 FA 11 - Cal State LA
ch15 FA 11 - Cal State LA

... – G-alpha-q increases activity of the effector Phospholipase C (PLC) • PI(4,5)P2 --> DAG + IP3 • DAG and IP3 are both 2nd messengers – G-alpha-12/13 is not well understood, but is linked to cancer ...
Chapter 34
Chapter 34

... The source of electrical potentials in neurons • Nerve impulses consist of electrical signals that are transient changes in the electrical potential differences (voltages) across neuron membrane • Difference between Nernst potential and actual potential ...
Chemical messengers 2007
Chemical messengers 2007

... with the receptor then bind with other proteins in a cascade – In each cascade, at some point, they all involve activation of proteins in the cytoplasm by phosphorylation. ...
The TNF and TNFR superfamilies
The TNF and TNFR superfamilies

... Tumor-necrosis factor (TNF) was discovered as a serum factor that was able to kill cancer cells in mice. The TNF receptor (TNFR) led to the discovery of a superfamily of transmembrane proteins. There are 18 ligands and 28 receptors many of which are being targeted for therapeutic purposes. TNFR sig ...
Unit 2 review sheets
Unit 2 review sheets

...  alpha 1 (eye and most blood vessels)  Beta (1 and 2; heart and lung, respectively)  Beta 3- found on adipose tissue  These receptors are metabotropic and would use the cAMP pathway ...
GABRA1 (gamma-aminobutyric acid (GABA) A receptor. alpha 1
GABRA1 (gamma-aminobutyric acid (GABA) A receptor. alpha 1

... GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors. which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GA Function: GABA, the major inhibitory neurotr ...
schiz drugs
schiz drugs

... which connect the prefrontal cortex with subcorticol areas, including the striatum, caudate, putmen and hippocampus.  The prefrontal cortical and limbic (hippocampus) link may represent the key vulnerability for development of schizophrenia, which has long been considered to be a disorder of cognit ...
Typical Signal Transduction Pathway
Typical Signal Transduction Pathway

... • Enduring Understanding 3.D Cells communicate by generating, transmitting and receiving chemical signals. • EK 3D2: Cells communicate with each other through direct contact with other cells or from a distance via chemical signaling c. Signals released by one cell type can travel long distances to ...
Mechanisms of cell communication
Mechanisms of cell communication

... activity of adenyl cyclase rather than decreasing the activity of phosphodiesterase. All receptors that act via cAMP are coupled to a stimulatory G protein (Gs), which activates adenyl cyclase. ...
SPA Receptor Binding Study Design
SPA Receptor Binding Study Design

... bead addition, T0 addition, or delayed addition. Pre-coupling affords the measure of “on” and “off” rates for receptor binding. The T0 addition format involves sequential addition of test samples, radio-ligand, membrane and bead as separate additions. The coupling of membrane to beads occurs simulta ...
Hole`s Human Anatomy and Physiology
Hole`s Human Anatomy and Physiology

... Temperature Senses • Two groups of free nerve endings located in the skin • Heat receptors respond to temperatures between 25 and 45 degrees C • Cold receptors respond between 10 and 20 degrees C • Outside of these ranges, pain receptors are stimulated ...
ch12a - TeacherWeb
ch12a - TeacherWeb

... Temperature Senses • Two groups of free nerve endings located in the skin • Heat receptors respond to temperatures between 25 and 45 degrees C • Cold receptors respond between 10 and 20 degrees C • Outside of these ranges, pain receptors are stimulated ...
Document
Document

... • Part of the GPCR C-terminus is tethered to the membrane by palmitoylation through a thioester linkage to a conserved Cys. • The G protein  subunit has myristate attached via an amide linkage to an N-terminal Gly to effect membrane association. • The G protein  subunit is incorporated into the me ...
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Cannabinoid receptor type 1

The cannabinoid receptor type 1, often abbreviated as CB1, is a G protein-coupled cannabinoid receptor located primarily in the central and peripheral nervous system. It is activated by the endocannabinoid neurotransmitters anandamide and 2-arachidonoylglycerol (2-AG); by plant cannabinoids, such as the compound THC, an active ingredient of the psychoactive drug cannabis; and by synthetic analogues of THC.
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