high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A; HCP1; TM22 (PDE7A)
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Function
- hydrolyzes the second messenger cAMP
- may have a role in muscle signal transduction
- purine metabolism; 3',5'-cyclic AMP degradation; AMP from 3',5'-cyclic AMP: step 1/1
- interacts with CBFA2T3
adenosine 3',5'-cyclic phosphate + H2O = adenosine 5'-phosphate
- binds 2 divalent metal cations per subunit
- site 1 may preferentially bind Zn+2
- site 2 has a preference for Mg+2 &/or Mn+2
Inhibition:
- insensitive to all selective PDE inhibitors
Structure
- composed of a C-terminal catalytic domain containing two putative divalent metal sites & an N-terminal regulatory domain
- belongs to the cyclic nucleotide phosphodiesterase family, PDE7 subfamily
Compartment
Alternative splicing
named isoforms=3; PDE7A1, PDE7A2, PDE7A3
Expression
- PDE7A1
- high expression in skeletal muscle
- low expression in brain & heart
- expressed as well in two T-cell lines
- PDE7A2
- high expression in skeletal muscle
- low expression in heart
- developmentally regulated
- PDE7A1 & PDE7A2 are found in several fetal tissues
- expression is reduced throughout development
- persists strongly only in adult skeletal muscle