3.5.4.5: cytidine deaminase
This is an abbreviated version!
For detailed information about cytidine deaminase, go to the full flat file.
Word Map on EC 3.5.4.5
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3.5.4.5
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hypermutation
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immunoglobulin
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deamination
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ige
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b-cells
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lymphocyte
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leukemia
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lymphoma
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diversification
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class-switched
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apobec3g
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immunodeficiency
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deaminases
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uracil
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gemcitabine
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single-stranded
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uridine
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isotype
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virion
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arabinoside
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cytarabine
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retroviruses
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ssdna
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glycosylase
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lymphomagenesis
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deoxyuridine
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cd40l
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encapsidation
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1-beta-d-arabinofuranosylcytosine
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deoxycytidylate
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c-to-u
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blimp-1
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nickase
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mrna-editing
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capecitabine
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polypeptide-like
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uracil-dna
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microhomology
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abasic
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medicine
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5-aza-cdr
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drug development
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protospacer
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diagnostics
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5'-deoxy-5-fluorouridine
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5\'-dfur
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plasmablast
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retroelements
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zebularine
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ara-ctp
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t-independent
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anti-cd40
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unmutated
- 3.5.4.5
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hypermutation
- immunoglobulin
-
deamination
- ige
- b-cells
- lymphocyte
- leukemia
- lymphoma
-
diversification
-
class-switched
- apobec3g
- immunodeficiency
- deaminases
- uracil
- gemcitabine
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single-stranded
- uridine
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isotype
- virion
- arabinoside
- cytarabine
- retroviruses
- ssdna
- glycosylase
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lymphomagenesis
- deoxyuridine
- cd40l
-
encapsidation
- 1-beta-d-arabinofuranosylcytosine
- deoxycytidylate
-
c-to-u
-
blimp-1
-
nickase
-
mrna-editing
- capecitabine
-
polypeptide-like
-
uracil-dna
-
microhomology
-
abasic
- medicine
-
5-aza-cdr
- drug development
-
protospacer
- diagnostics
- 5'-deoxy-5-fluorouridine
-
5\'-dfur
-
plasmablast
-
retroelements
- zebularine
- ara-ctp
-
t-independent
-
anti-cd40
-
unmutated
Reaction
Synonyms
activation-induced cytidine deaminase, AICDA, canine hepatic cyd deaminase, CDA, CDABcald, CDABpsy, CDABsub, CDase, CDD, CR deaminase, cyd deaminase, Cytidine aminohydrolase, cytidine deaminase, cytidine/2'-deoxycytidine aminohydrolase, cytosine nucleoside deaminase, DCD, dCDA, deoxycytidine deaminase, EC 3.5.4.14, mammalian deminase, T-CDA, yeast cytidine deaminase
ECTree
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Crystallization
Crystallization on EC 3.5.4.5 - cytidine deaminase
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crystal structure of tetrameric cytidine deaminase at 2.0 A resolution, hanging drop vapour-diffusion method
hanging drop vapour diffusion method. R56A and R56Q crystallize in the same space group as the wild-type enzyme with two subunits in the asymmetric unit, whereas C53H/R56Q can not crystallize in this crystal form but is crystallized in another space group, P3(2)21, with a full tetramer in the asymmetric unit
comparison of theoretically predicited model and experimentally elucidated structure
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in complex with inhibitor diazepinone riboside. Inhibitor is able to establish a canonical pi/pi interaction with key active site residue F137
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to 2.07 A resolution. Two 1,4-dioxane moleules are present at the active site
in complex with tetrahydrouridine, 3-deazauridine, or cytidine. Two alternate conformations of R68 influence zinc-product interaction
purified recombinant CDA complexed with either tetrahydrouridine, 3-deazauridine, or cytidine, hanging drop vapor diffusion technique, 25°C, protein solution, containing 10-15 mg/ml protein in 20 mM Tris-HCl, pH 7.5, 1 mM DTT, and 5 mM ligand, is mixed with crystallization solution containing 2.0 M ammonium sulfate and 0.1 M Tris-HCl, pH 8.5, crystals appear after a few hours or several days, respectively, X-ray diffraction structure determination and analysis at 1.48-2.36 A resolutions, molecular replacement
purified CDA in complex with uridine and deoxyuridine, hanging drop vapor diffusion method, 0.002 ml of 12 mg/ml protein in 20 mM Tris-HCl pH 7.5 is mixed with 0.002 ml of reservoir solution containing 0.1 M HEPES, pH 7.5 and 4.3 M sodium chloride, ligands uridine and deoxyuridine are added by soaking method, X-ray diffractiuon structure determination and analysis at 2.4 and 1.9 A resolution,molecular dynamics simulation, structure modeling