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Literature summary extracted from

  • Yuan, H.; Chai, S.C.; Lam, C.K.; Howard Xu, H.; Ye, Q.Z.
    Two methionine aminopeptidases from Acinetobacter baumannii are functional enzymes (2011), Bioorg. Med. Chem. Lett., 21, 3395-3398.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

EC Number Cloned (Comment) Organism
3.4.11.18 His-tagged protein expressed in Escherichia coli BL21(DE3) Acinetobacter baumannii

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.4.11.18 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
-
Acinetobacter baumannii
3.4.11.18 4-(3-methylthiophen-2-yl)benzene-1,2-diol
-
Acinetobacter baumannii
3.4.11.18 5-(2,5-dichlorophenyl)furan-2-carboxylic acid
-
Acinetobacter baumannii
3.4.11.18 5-(2-chlorophenyl)furan-2-carboxylic acid
-
Acinetobacter baumannii
3.4.11.18 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
-
Acinetobacter baumannii
3.4.11.18 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
-
Acinetobacter baumannii
3.4.11.18 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
-
Acinetobacter baumannii

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
3.4.11.18 0.111
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.115
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.13
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.144
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.154
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.155
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.161
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.168
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
3.4.11.18 Fe2+ activator after removal of divalent metal ions with Chelex-100 Acinetobacter baumannii
3.4.11.18 Fe2+ activator after removal of divalent metal ions with EDTA Acinetobacter baumannii
3.4.11.18 Ni2+ activator after removal of divalent metal ions with Chelex-100 Acinetobacter baumannii
3.4.11.18 Ni2+ activator after removal of divalent metal ions with EDTA, less efficient than Fe2+ Acinetobacter baumannii

Organism

EC Number Organism UniProt Comment Textmining
3.4.11.18 Acinetobacter baumannii A0A1E3MBK2
-
-
3.4.11.18 Acinetobacter baumannii ATCC 17978 A0A1E3MBK2
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
3.4.11.18 immobilized metal ion affinity chromatography (Ni2+) Acinetobacter baumannii

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.4.11.18 Met-4-methylcoumaryl-7-amide + H2O
-
Acinetobacter baumannii Met + 7-amino-4-methylcoumarin
-
?
3.4.11.18 Met-4-methylcoumaryl-7-amide + H2O
-
Acinetobacter baumannii ATCC 17978 Met + 7-amino-4-methylcoumarin
-
?

Synonyms

EC Number Synonyms Comment Organism
3.4.11.18 methionine aminopeptidase AbMetAPx
-
Acinetobacter baumannii
3.4.11.18 methionine aminopeptidase AbMetAPy
-
Acinetobacter baumannii

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
3.4.11.18 0.0000508
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000055
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000137
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000159
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000263
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000305
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000312
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000449
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.4.11.18 0.00038
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.0004
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.00051
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.00064
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.00065
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.00078
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.00088
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.00092
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.00095
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.0021
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.0022
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.0038
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.0044
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.0049
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.0061
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2,5-dichlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.0071
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2,5-dichlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.013
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.014
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.021
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.022
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.023
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.024
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.027
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.03
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.032
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.033
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.034
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.034
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.039
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.044
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.055
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(3-methylthiophen-2-yl)benzene-1,2-diol
3.4.11.18 0.056
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.064
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.072
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.079
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 4-(2-methyl-1,3-thiazol-4-yl)benzene-1,2-diol
3.4.11.18 0.094
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.103
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.128
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(2,4-dichlorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.145
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-methylbenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.186
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.188
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.251
-
after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2,5-dichlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.286
-
after removal of divalent metal ions activated with 0.02 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2,5-dichlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.288
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.303
-
after removal of divalent metal ions activated with 0.02 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-[(4-fluorobenzyl)sulfanyl]-4H-1,2,4-triazol-3-amine
3.4.11.18 0.355
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2,5-dichlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.358
-
after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.381
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.394
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2-chlorophenyl)furan-2-carboxylic acid
3.4.11.18 0.494
-
after removal of divalent metal ions activated with 0.02 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii 5-(2,5-dichlorophenyl)furan-2-carboxylic acid

kcat/KM [mM/s]

EC Number kcat/KM Value [1/mMs-1] kcat/KM Value Maximum [1/mMs-1] Substrate Comment Organism Structure
3.4.11.18 0.00033
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000479
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Mn2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.000948
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.00105
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Co2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.0017
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.00217
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.020 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.00275
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.005 mM Ni2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii
3.4.11.18 0.00278
-
Met-4-methylcoumaryl-7-amide after removal of divalent metal ions activated with 0.0025 mM Fe2+, pH not specified in the publication, temperature not specified in the publication Acinetobacter baumannii