3.5.1.11: penicillin amidase
This is an abbreviated version!
For detailed information about penicillin amidase, go to the full flat file.
Word Map on EC 3.5.1.11
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3.5.1.11
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6-aminopenicillanic
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phenylacetic
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biocatalyst
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anandamide
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acylases
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cannabinoids
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cephalosporin
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synthesis
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binuclear
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alcaligenes
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cephalexin
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megaterium
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endocannabinoids
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semi-synthetic
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3.5.1.1
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kluyvera
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l-asparagine
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dihydroorotase
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phenylacetylated
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allantoinase
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dihydropyrimidinase
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lactonase
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amoxicillin
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rettgeri
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eupergit
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multipoint
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acyl-enzyme
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asparaginase
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hydantoinase
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phenoxyacetic
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aminoacylase
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7-aminocephalosporanic
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phosphotriesterase
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sphaericus
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hydantoin
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providencia
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n-acylethanolamines
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penicillanic
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dihydrouracil
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cleas
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pharmacology
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industry
- 3.5.1.11
-
6-aminopenicillanic
-
phenylacetic
-
biocatalyst
- anandamide
- acylases
- cannabinoids
- cephalosporin
- synthesis
-
binuclear
- alcaligenes
- cephalexin
- megaterium
-
endocannabinoids
-
semi-synthetic
-
3.5.1.1
-
kluyvera
- l-asparagine
- dihydroorotase
-
phenylacetylated
- allantoinase
- dihydropyrimidinase
- lactonase
- amoxicillin
- rettgeri
-
eupergit
-
multipoint
- acyl-enzyme
- asparaginase
- hydantoinase
-
phenoxyacetic
-
aminoacylase
-
7-aminocephalosporanic
- phosphotriesterase
- sphaericus
- hydantoin
- providencia
- n-acylethanolamines
-
penicillanic
- dihydrouracil
-
cleas
- pharmacology
- industry
Reaction
Synonyms
ACPGA001 PGA, AfPGA, alpha-acylamino-beta-lactam acylhydrolase, amidase, amidohydrolase, ampicillin acylase, AuAAC, benzylpenicillin acylase, BmPGA, Eca3205, KcPGA, maPGA, More, novozym 217, PA, PAC, penicillin acylase, penicillin amidase, Penicillin amidohydrolase, penicillin G acylase, Penicillin G amidase, Penicillin G amidohydrolase, penicillin V acylase, Penicillin V amidase, penicillin-G acylase, PGA, PGA650, PVA, semacylase, Sm-PVA, YxeI
ECTree
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Reaction
Reaction on EC 3.5.1.11 - penicillin amidase
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penicillin + H2O = a carboxylate + 6-aminopenicillanate
F24 in beta-subunit has a fixed position, whereas F146 of alpha-subunit acts as a flexible lid on the binding site
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penicillin + H2O = a carboxylate + 6-aminopenicillanate
structural model and catalytic mechanism, and energetics of the reaction, acylation is the rate-limiting step of hydrolysis. The collapse of the tetrahedral intermediate proceeds via synchronous bond breaking and formation, and the accumulation of charge on the amidic nitrogen due to the presence of a substituent is disfavored
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