3.2.2.6: ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase
This is an abbreviated version!
For detailed information about ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase, go to the full flat file.
Word Map on EC 3.2.2.6
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3.2.2.6
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cadpr
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ryanodine
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aplysia
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inositol
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naadp
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ectoenzyme
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ca2+-mobilizing
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californica
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gdp-ribose
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nadase
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beta-nad+
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urchin
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diphosphoribose
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calcium-mobilizing
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8-br-cadpr
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oxytocin
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ca2+-releasing
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anti-cd38
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trisphosphate
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8-bromo-cadpr
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ca2+-induced
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nad+-glycohydrolase
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ngd+
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ryanodine-sensitive
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cd38-deficient
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cadpr-mediated
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cadpr-induced
- 3.2.2.6
-
cadpr
-
ryanodine
- aplysia
- inositol
-
naadp
-
ectoenzyme
-
ca2+-mobilizing
- californica
- gdp-ribose
- nadase
- beta-nad+
-
urchin
- diphosphoribose
-
calcium-mobilizing
-
8-br-cadpr
- oxytocin
-
ca2+-releasing
-
anti-cd38
-
trisphosphate
-
8-bromo-cadpr
-
ca2+-induced
- nad+-glycohydrolase
- ngd+
-
ryanodine-sensitive
-
cd38-deficient
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cadpr-mediated
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cadpr-induced
Reaction
Synonyms
ADP-ribosyl cyclase, ADPR cyclase, bCD38, CD38, CD38/NAD+ glycohydrolase, NAD(P) nucleosidase, NAD(P)+ glycohydrolase, NAD(P)+-glycohydrolase, NAD(P)-glycohydrolase, NAD(P)ase, NAD+ glycohydrolase, NADase, nicotinamide adenine dinucleotide (phosphate) glycohydrolase, nicotinamide adenine dinucleotide (phosphate) nucleosidase, nucleosidase, nicotinamide adenine dinucleotide (phosphate), triphosphopyridine nucleotidase
ECTree
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Crystallization
Crystallization on EC 3.2.2.6 - ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase
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mono N-glycosylated forms of soluble enzyme ecto-domain (residues 32-278) and catalytic residue mutant Glu218Gln, in apo state or bound to 2'-fluorinated NAD+ derivatives aFNAD or rFNAD, hanging drop vapour diffusion method, from 20-30% PEG 4000, 50-250 mM ammonium sulfate and 100 mM sodium cacodylate, sodium acetate or MES, pH 6.0-6.5, room temperature, soaking of crystals in 1-3 mM ligand solution, X-ray diffraction structure determination and analysis at 1.8 A resolution, molecular replacement
enzyme in complex with inhibitors, hanging drop vapor diffusion method, mixing of 10 mg/ml protein in 20 mM HEPES with 5 mm ligands, with reservoir solution containing 0.1 M sodium acetate, pH 4.0, 0.2 M ammonium acetate, 3% 2-propanol, and 15% PEG 10000, X-ray diffraction structure determination and analysis, molecular replacement