cAMP-specific 3',5'-cyclic phosphodiesterase 7B (PDE7B)
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Function
- hydrolyzes the second messenger cAMP
- may be involved in the control of cAMP-mediated neural activity & cAMP metabolism in the brain
- purine metabolism; 3',5'-cyclic AMP degradation; AMP from 3',5'-cyclic AMP: step 1/1
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 (putative)
Inhibition:
- inhibited by dipyridamole, IBMX & SCH 51866
- insensitive to zaprinast, rolipram, & milrinone
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
Expression
- highly expressed in brain
- also expressed in heart, liver, skeletal muscle & pancreas