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AMP deaminase

AMP deaminase plays a critical role in energy metabolism.

Below are the list of possible AMP deaminase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.

AMP deaminase 1

Also known as AMP deaminase 1 (AMP deaminase isoform M) (Myoadenylate deaminase).
AMPD1: AMP deaminase plays a critical role in energy metabolism. Defects in AMPD1 are the cause of adenosine monophosphate deaminase deficiency muscle type (AMPDDM). AMPDDM is a metabolic disorder resulting in exercise-related myopathy. It is characterized by exercise-induced muscle aches, cramps, and early fatigue. Belongs to the adenosine and AMP deaminases family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 3.5.4.6; Hydrolase; Nucleotide Metabolism - purine

Molecular Function: AMP deaminase activity; myosin heavy chain binding

Biological Process: response to organic substance

AMP deaminase 2

Also known as AMP deaminase 2 (AMP deaminase isoform L).
AMPD2: AMP deaminase plays a critical role in energy metabolism. Belongs to the adenosine and AMP deaminases family. 4 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 3.5.4.6; Hydrolase; Nucleotide Metabolism - purine

Molecular Function: AMP deaminase activity

Biological Process: AMP metabolic process; ATP metabolic process; cholesterol homeostasis; GTP metabolic process; IMP biosynthetic process; nucleotide metabolic process

AMP deaminase 3

Also known as AMP deaminase 3 (AMP deaminase H-type) (AMP deaminase isoform E) (Heart-type AMPD).
AMPD3: AMP deaminase plays a critical role in energy metabolism. Defects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders. Belongs to the adenosine and AMP deaminases family. 6 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 3.5.4.6; Hydrolase; Nucleotide Metabolism - purine

Molecular Function: AMP deaminase activity

Biological Process: ADP metabolic process; AMP metabolic process; ATP metabolic process; erythrocyte homeostasis; GTP metabolic process; IMP biosynthetic process
Proteins Root Name Listing
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