2.5.1.63: adenosyl-fluoride synthase
This is an abbreviated version!
For detailed information about adenosyl-fluoride synthase, go to the full flat file.
Word Map on EC 2.5.1.63
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2.5.1.63
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cattleya
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fluorometabolite
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tomography
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positron
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fluoroacetate
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4-fluorothreonine
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synthesis
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transhalogenation
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halide
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chlorinase
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tropica
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organofluorine
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5'-chloro-5'-deoxyadenosine
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biotechnology
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radiosynthesis
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salinispora
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desolvation
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analysis
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bond-forming
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halogenase
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18f-fluoride
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carbon-fluorine
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pharmacology
- 2.5.1.63
- cattleya
-
fluorometabolite
-
tomography
-
positron
- fluoroacetate
-
4-fluorothreonine
- synthesis
-
transhalogenation
- halide
- chlorinase
- tropica
-
organofluorine
- 5'-chloro-5'-deoxyadenosine
- biotechnology
-
radiosynthesis
-
salinispora
-
desolvation
- analysis
-
bond-forming
- halogenase
-
18f-fluoride
-
carbon-fluorine
- pharmacology
Reaction
Synonyms
5'-deoxy-5'-fluoroadenosine synthase, 5'-FDA synthase, 5'-FDAS, 5'-fluoro-5'-deoxy adenosine synthetase, 5'-fluoro-5'-deoxyadenosine synthase, 5’-fluorodeoxyadenosine synthase, adenosyl-fluoride synthase, FDAS, flA, flA protein, FlA1, FlA4, fluorinase, fluorinase enzyme, fluorinase, S-adenosyl-L-methionine, fluorination enzyme, NobA, SAM fluorinase, SAMN04487820_1174
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Reaction
Reaction on EC 2.5.1.63 - adenosyl-fluoride synthase
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S-adenosyl-L-methionine + fluoride = 5'-deoxy-5'-fluoroadenosine + L-methionine
reaction mechanism, inversion of configuration consistent with a SN2 reaction mechanism
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S-adenosyl-L-methionine + fluoride = 5'-deoxy-5'-fluoroadenosine + L-methionine
substrate binding structure involving F156, S158, Y177, and T80, nucleophilic substitution reaction mechanism
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S-adenosyl-L-methionine + fluoride = 5'-deoxy-5'-fluoroadenosine + L-methionine
C-F bond formation, the enzyme catalyses an SN2 type reaction mechanism
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S-adenosyl-L-methionine + fluoride = 5'-deoxy-5'-fluoroadenosine + L-methionine
reaction mechanism, overview
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S-adenosyl-L-methionine + fluoride = 5'-deoxy-5'-fluoroadenosine + L-methionine
SN2 substitution reaction mechanism, where fluoride ion mediates a nucleophilic attack to the 5'-carbon of the ribose ring of S-adenosyl-L-methionine to give 5'-deoxy-5'-fluoroadenosine. The reaction proceeds with an inversion of configuration at the C-5'carbon