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| also known as adenylyl cyclase, an enzyme that catalyzes the conversion of ATP to cAMP |
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| q(adenosine monophosphate)consists of a phosphate group, a ribose, and the nucleoside andenosine, it can be produced during ATP synthesis orduring hydrolysis of ATP or ADP |
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| qg-protein receptor that stimulates phospholipase C activity. It is also refered to as the alpha adrenergic agonist receptor. |
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| a calcium binding protein, when calcium binds to the protein it can then associate with other proteins(enzymes) and modify their activities. |
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| a large, branched polysaccharide that is the storage form of glucose. It's breakdown is exergonic and releases energy while also incresing blood glucose levels. |
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| the breakdown of glycogen into glucose, takes place in muscle and liver tissues |
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| An inborn deficiency of muscle phosphorylase, causing an abnormal accumulation of glycogen in muscle tissue. (www.whonamedit.com McArdle's disease) |
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Term
| signal transduction system - |
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Definition
| starts with a signal to a receptor, and ends with a change in cell function |
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Term
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Definition
| Disease where the body cannot break down glycogen for energy (Type I glycogen storage disease (GSD I)). (medline plus) |
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Term
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Definition
| also known as adenylyl cyclase, an enzyme that catalyzes the conversion of ATP to cAMP |
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Term
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Definition
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Term
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Definition
| q(adenosine monophosphate)consists of a phosphate group, a ribose, and the nucleoside andenosine, it can be produced during ATP synthesis orduring hydrolysis of ATP or ADP |
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Term
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Definition
| qg-protein receptor that stimulates phospholipase C activity. It is also refered to as the alpha adrenergic agonist receptor. |
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Definition
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Definition
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Definition
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| a calcium binding protein, when calcium binds to the protein it can then associate with other proteins(enzymes) and modify their activities. |
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| cAMP-dependent protein kinase |
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| a large, branched polysaccharide that is the storage form of glucose. It's breakdown is exergonic and releases energy while also incresing blood glucose levels. |
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Definition
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| glycogen storage diseases |
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Definition
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Definition
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Definition
| the breakdown of glycogen into glucose, takes place in muscle and liver tissues |
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Definition
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| hepatic protein phosphatase-1 |
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| An inborn deficiency of muscle phosphorylase, causing an abnormal accumulation of glycogen in muscle tissue. (www.whonamedit.com McArdle's disease) |
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Definition
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| phosphatidyl inositol bisphosphate |
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| signal transduction system - |
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Definition
| starts with a signal to a receptor, and ends with a change in cell function |
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Definition
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Definition
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| UDP-glucose pyrophosphorylase |
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Definition
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Definition
| Disease where the body cannot break down glycogen for energy (Type I glycogen storage disease (GSD I)). (medline plus) |
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