3.5.1.85: (S)-N-acetyl-1-phenylethylamine hydrolase

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For detailed information about (S)-N-acetyl-1-phenylethylamine hydrolase, go to the full flat file.

Word Map on EC 3.5.1.85

3.5.1.85

meat

transl

tripolyphosphatase

minced

comminuted

adomet

diphosphatase

s-adenosylmethionine

rigor

barbituric

pyrimidine

synthesis

Reaction

Synonyms

(S)-N-acetyl-1-phenylethylamine amidohydrolase, (S)-specific acylase, (S)-specific N-acetyl-1-phenylethylamine amidohydrolase, hydrolase, (S)-N-acetyl-1-phenylethylamine

ECTree

3 Hydrolases

3.5 Acting on carbon-nitrogen bonds, other than peptide bonds

3.5.1 In linear amides

3.5.1.85 (S)-N-acetyl-1-phenylethylamine hydrolase

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Results	in table
1	Activating Compound
2	Application
1	CAS Registry Number
13	Inhibitors
1	KM Value [mM]
1	Metals/Ions
2	Molecular Weight [Da]
2	Organism
3	pH Optimum
3	pH Range
2	pH Stability
1	Purification (Commentary)
3	Reaction
1	Reaction Type
2	Reference
1	Specific Activity [micromol/min/mg]
10	Substrates and Products (Substrate)
2	Subunits
4	Synonyms
1	Systematic Name
1	Temperature Optimum [°C]
3	Temperature Stability [°C]

Inhibitors

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Inhibitors on EC 3.5.1.85 - (S)-N-acetyl-1-phenylethylamine hydrolase

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Ba2+

1 mM: 5% inhibition

Ca2+

1 mM: 10% inhibition

Cd2+

1 mM: 15% inhibition

Co2+

1 mM: 31% inhibition

Cu2+

1 mM: 12% inhibition

Mg2+

1 mM: 10% inhibition

Mn2+

1 mM: 13% inhibition

Ni2+

1 mM: 60% inhibition

Pb2+

1 mM: 5% inhibition

phenylmethylsulfonyl fluoride

Rhodococcus equi

strong inhibition, 0.1 mM: 95% inhibition, 0.01 mM: 84% inhibition

V3+

1 mM: 11% inhibition

Zn2+

1 mM: 32% inhibition

additional information

Rhodococcus equi

no inhibition by 10 mM chelating agents: EDTA, citrate and 10 mM thiol-reducing agents: dithiothreitol, mercaptoethanol, reduced glutathione; no inhibition by 1 mM Fe3+

209241