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UniProt functional annotation for Q9QYJ6 | ||
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| UniProt code: Q9QYJ6. |
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| Organism: | |
Rattus norvegicus (Rat). |
| Taxonomy: | |
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus. |
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| Function: | |
Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. Can hydrolyze both cAMP and cGMP, but has higher affinity for cAMP and is more efficient with cAMP as substrate. {ECO:0000269|PubMed:10583409}. |
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| Catalytic activity: | |
Reaction=a nucleoside 3',5'-cyclic phosphate + H2O = a nucleoside 5'- phosphate + H(+); Xref=Rhea:RHEA:14653, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:57867, ChEBI:CHEBI:58464; EC=3.1.4.17; Evidence={ECO:0000269|PubMed:10583409, ECO:0000269|PubMed:14752115}; |
| Catalytic activity: | |
Reaction=3',5'-cyclic AMP + H2O = AMP + H(+); Xref=Rhea:RHEA:25277, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:58165, ChEBI:CHEBI:456215; Evidence={ECO:0000269|PubMed:10583409}; |
| Catalytic activity: | |
Reaction=3',5'-cyclic GMP + H2O = GMP + H(+); Xref=Rhea:RHEA:16957, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:57746, ChEBI:CHEBI:58115; Evidence={ECO:0000269|PubMed:10583409, ECO:0000269|PubMed:14752115}; |
| Cofactor: | |
Name=a divalent metal cation; Xref=ChEBI:CHEBI:60240; Note=Binds 2 divalent metal cations per subunit. Site 1 may preferentially bind zinc ions, while site 2 has a preference for magnesium and/or manganese ions.; |
| Activity regulation: | |
Inhibited by dipyridamole and moderately by IBMX, zaprinast and rolipram. {ECO:0000269|PubMed:10583409}. |
| Biophysicochemical properties: | |
Kinetic parameters: KM=0.26 uM for cAMP {ECO:0000269|PubMed:10583409}; KM=9.3 uM for cGMP {ECO:0000269|PubMed:10583409}; |
| Pathway: | |
Purine metabolism; 3',5'-cyclic AMP degradation; AMP from 3',5'-cyclic AMP: step 1/1. |
| Pathway: | |
Purine metabolism; 3',5'-cyclic GMP degradation; GMP from 3',5'-cyclic GMP: step 1/1. |
| Subunit: | |
Homodimer. {ECO:0000250}. |
| Subcellular location: | |
Cytoplasm {ECO:0000269|PubMed:10583409}. |
| Tissue specificity: | |
Detected in striatum and testis (at protein level). Detected in whole brain, hippocampus, olfactory bulb, striatum neurons and testis. {ECO:0000269|PubMed:10583409, ECO:0000269|PubMed:14752115}. |
| Induction: | |
Up-regulated in brain after seizures. Up-regulated in the hippocampus one hour after induction of long-term potentiation. {ECO:0000269|PubMed:14752115}. |
| Domain: | |
The tandem GAF domains bind cAMP, and regulate enzyme activity. The binding of cAMP stimulates enzyme activity. |
| Domain: | |
Composed of a C-terminal catalytic domain containing two divalent metal sites and an N-terminal regulatory domain which contains one cyclic nucleotide-binding region. |
| Similarity: | |
Belongs to the cyclic nucleotide phosphodiesterase family. {ECO:0000305}. |
Annotations taken from UniProtKB at the EBI.