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8-hydroxyquinoline
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0.1 mM at pH 10, 5 mM at pH 7
Ac-Val-Leu-Lys-4-mercaptoanilide
-
pH 7.8, 37°C, 0.2 mM 69% inhibition, 0.3 mM complete inhibition
alkaline protease inhibitor
-
-
-
antipain
-
only Serratia marcescens MW 56000 enzyme
APRin protein
-
slow binding inhibition, reversible inhibition. and truncated mutants
-
benzalkonium chloride
-
-
benzyloxycarbonyl-D-Ala-Leu-Ala
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competitive to benzyloxycarbonyl-Ala-Phe-Gly-Ala
Benzyloxycarbonyl-Gly-Leu-D-Ala
-
benzyloxycarbonyl-Ala-Phe-Gly-Ala as substrate
Benzyloxycarbonyl-Gly-Leu-Gly
-
benzyloxycarbonyl-Ala-Phe-Gly-Ala as substrate
Benzyloxycarbonyl-Gly-Leu-NH2
-
benzyloxycarbonyl-Ala-Phe-Gly-Ala as substrate
Benzyloxycarbonyl-Phe-D-Leu-Ala
-
competitive to benzyloxycarbonyl-Ala-Phe-Gly-Ala
Bovine pancreatic trypsin inhibitor
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0.01 mM, 5% inhibition at pH 5.5
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captopril
-
0.001 mM, 82% residual activity
Cd2+
-
at pH 10, not at pH 7
chymostatin
-
0.1 mM, 18% inhibition at pH 8.0
diisopropylfluorophosphate
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1 mM, weak inhibition at pH 5.5 and pH 8.0 with and without addition of 1 mM Co2+
dithiothreitol
5 mM, 5% residual activity
DTNB
-
reversible, synergism with pyridoxal 5'-phosphate or phenylglyoxal
E-64
-
0.0056 mM, 91% residual activity
Elastatinal
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0.1 mM, 11% inhibition at pH 8.0 and without 1 mM Co2+ addition
Guanidine-HCl
-
enhanced by EDTA
HgCl2
-
complete inhibition
L-trans-epoxysuccinyl-leucyl-amido-(4-guanido)butane
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0.1 mM, 26% inhibition at pH 8.0 and 1 mM Co2+ addition, 26% inhibition at pH 5.5 without addition of 1 mM Co2+
L3A SmaPI
-
mutant inhibitor
-
L3D SmaPI
-
mutant inhibitor
-
L3F SmaPI
-
mutant inhibitor
-
L3G SmaPI
-
mutant inhibitor
-
L3I SmaPI
-
mutant inhibitor
-
L3K SmaPI
-
mutant inhibitor
-
L3P SmaPI
-
mutant inhibitor
-
Mg2+
-
10 mM, 93% residual activity
N-tosyl-L-phenylalanine chloromethyl ketone
-
0.1 mM, 18% inhibition at pH 8.0
Ni2+
-
at pH 10, not at pH 7
p-hydroxymercuribenzoate
-
0.002 mM, 71% residual activity
Periplasmic endogen inhibitor peptide of Serratia marcescens
-
Phenanthroline
-
strong inhibition with 4.65% residual activity at 10 mM
phenyl-methanesulfonyl fluoride
-
1 mM, 14-17% inhibition at pH 5.5 and pH 8.0 with and without addition of 1 mM Co2+
Phenylglyoxal
-
synergism with DTNB
phenylmethylsulfonyl fluoride
phosphoramidon
-
0.1 mM, no inhibition at pH 8.0 and 1 mM Co2+ addition, 25% inhibition at pH 8.0 and 5.5 without addition of 1 mM Co2+
pyridoxal 5'-phosphate
-
synergism with DTNB
SmaPI
-
Serratia marcescens metalloprotease inhibitor, wild-type
-
SmaPIAddA
-
mutant inhibitor
-
SmaPIDelG
-
mutant inhibitor
-
SmaPIDelG1-L3
-
mutant inhibitor
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SmaPIDelG1-S2
-
mutant inhibitor
-
Sn2+
-
59.07% residual activity at 5 mM
Soybean trypsin inhibitor
-
0.01 mM, 9% inhibition at pH 5.5
-
Tetraethylenepentamine
-
zinc-specific chelator
Tetramethylenepentamine
-
Serratia marcescens
1,10-phenanthroline
-
1 mM
1,10-phenanthroline
-
complete inhibition
1,10-phenanthroline
-
10 mM; strong
1,10-phenanthroline
-
30 min, room temperature, pH 7.5, complete and irreversible inhibition in a concentration range below 1 mM
1,10-phenanthroline
-
pH 7.8, 37°C, 1 mM 66% inhibition, 3mM 90% inhibition
1,10-phenanthroline
-
10 mM, strong inhibition at pH 5.5 and pH 8.0 with and without addition of 1 mM Co2+
1,10-phenanthroline
-
reversible by dialysis, Mg2+ or Co2+ partially restores; strong
1,10-phenanthroline
-
neither Ca2+, Zn2+ nor Fe2+ restores
1,10-phenanthroline
-
Serratia marcescens enzyme
1,10-phenanthroline
-
activity can be restored with the addition of Mn2+, Cu2+ and Co2+ up to 90-200% of its original value, while Zn2+ is inefficient
2,2'-bipyridyl
-
5 mM
Ca2+
-
inhibitory above 0.1 mM
Ca2+
-
10 mM, 90% residual activity
Co2+
-
inhibitory above 5 mM
Cu2+
-
-
Cu2+
-
10 mM, 58% residual activity
Cysteine hydrochloride
-
not Serratia marcescens enzyme
Cysteine hydrochloride
-
not Serratia marcescens enzyme
Cysteine hydrochloride
-
not Serratia marcescens enzyme
Cysteine hydrochloride
-
not Serratia marcescens enzyme
Cysteine hydrochloride
-
not Serratia marcescens enzyme
Cysteine hydrochloride
-
weak
Cysteine hydrochloride
-
not Serratia marcescens enzyme
Cysteine hydrochloride
-
not Serratia marcescens enzyme
DTT
-
weak, Serratia marcescens
DTT
-
weak, Serratia marcescens
DTT
-
weak, Serratia marcescens
DTT
-
weak, Serratia marcescens
DTT
-
weak, Serratia marcescens
DTT
-
weak, Serratia marcescens
DTT
-
weak, Serratia marcescens
EDTA
-
0.1 mM at pH 10, 5 mM at pH 7
EDTA
-
complete inhibition
EDTA
-
Co2+; Mn2+; strong, 5 mM
EDTA
-
30 min, room temperature, pH 7.5, complete inhibition in a concentration range below 1 mM
EDTA
-
1 mmol, pH 8.1, no inactivation by 0.1 M EDTA
EDTA
-
10 mM, almost complete inactivation at pH 5.5 and pH 8.0 with and without addition of 1 mM Co2+
EDTA
5 mM, 23% residual activity
EDTA
-
10 mM, pH 8, strong inhibition
EDTA
-
Ca2+ (partially); Cu2+ restores partially; more effective at acidic pH; partially reversible by dialysis
EDTA
-
Ca2+ (not) restores; Fe2+ (not); Zn2+ (not)
EDTA
-
Ca2+ (MW 56000 and MW 60000 enzyme); Ca2+ (partially); Co2+ (Serratia sp. E-16 enzyme); Cu2+ (not); Fe2+ (only MW 56000 enzyme); Mg2+ (not); Serratia enzymes; Zn2+ (MW 56000 and MW 60000 enzyme)
EDTA
-
Ca2+ (restored activity higher than native activity); enhances inhibition by guanidine-HCl; Fe2+ (partially); Mg2+; Mn2+ (restored activity higher than native activity); no reactivation by K+; Zn2+ (restored activity higher than native activity)
EDTA
-
strong inhibition with 2.6% residual activity at 10 mM, enzyme activity can be regained by the addition of Co2+, Cu2+, Fe2+, Mg2+, and Zn2+ ions after chelation of ions with EDTA
EDTA
-
10 mM, 42% residual activity
EDTA
-
10 mM, 3% residual activity
EDTA
-
inhibits the activity only partially even either after long incubation or in excess amount
EGTA
-
complete inhibition
EGTA
5 mM, 33% residual activity
EGTA
-
10 mM, pH 8, strong inhibition
Fe2+
-
strong
Fe2+
-
68.66% residual activity at 5 mM
Hg2+
-
-
Hg2+
-
10 mM, 5.5% residual activity
iodoacetamide
-
0.1 mM, 72% residual activity
iodoacetamide
-
10 mM, 96% residual activity
KCN
-
at pH 10, no inhibition at pH 7.5
KMnO4
-
-
leupeptin
-
0.1 mM, 10% inhibition at pH 8.0 and 1 mM Co2+ addition, 7% inhibition at pH 8.0 without 1 mM Co2+ addition
leupeptin
-
weak, only Serratia marcescens MW 56000 enzyme
N-bromosuccinimide
-
strong
N-bromosuccinimide
-
strong
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
N-ethylmaleimide
-
0.1 mM, 14% inhibition at pH 8.0 and 1 mM Co2+ addition
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
N-ethylmaleimide
-
not (Serratia marcescens enzyme)
NaCl
1 M, 56% residual activity
NaCl
-
inhibitory effect depends on substrate
o-phenanthroline
0.5 mM, 10% residual activity
o-phenanthroline
-
2 mM, no residual activity
Pb2+
-
-
Periplasmic endogen inhibitor peptide of Serratia marcescens
-
-
-
Periplasmic endogen inhibitor peptide of Serratia marcescens
-
recombinant and native form, pH- and heat-stable protein, inhibition at 1:1 molar ratio, highly specific for Serratia marcescens proteinase, mechanism
-
phenylmethylsulfonyl fluoride
-
0.5 mM, 81% residual activity
phenylmethylsulfonyl fluoride
-
10 mM, 97% residual activity
PMSF
-
not
PMSF
-
weak, Serratia marcescens
Sodium thioglycolate
-
1 mM, at pH 10, no inhibition at pH 7.5
Sodium thioglycolate
-
not
Sodium thioglycolate
-
weak
Zn2+
-
inhibitory above 0.025 mM
Zn2+
-
both the Zn2+ inhibition of protease B activity and its resistance to EDTA inhibition might be caused by an Asp in position 191 where most of the serralysins contain Asn
additional information
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2-mercaptoethanol; diisopropyl phosphofluoridate; iodine, ovomucoid; monoiodoacetic acid; PCMB; potato inhibitor; soybean trypsin inhibitor
-
additional information
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-
-
additional information
-
not inhibitory: PMSF, E-64 and pepstatin
-
additional information
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diisopropyl phosphofluoridate; PCMB; potato inhibitor; soybean trypsin inhibitor; tosyl-L-Phe chloromethyl ketone or tosyl-L-Lys chloromethyl ketone
-
additional information
-
-
-
additional information
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citrate, NaF, oxalate; diisopropyl phosphofluoridate; monoiodoacetic acid; PCMB; potato inhibitor; soybean trypsin inhibitor
-
additional information
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not inhibited by chloromethylketone or hydroxamate
-
additional information
-
not inhibited by dithiothreitol, PMSF and DFP
-
additional information
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Lima bean, human pancreatic or egg white trypsin inhibitor, human alpha1-antitrypsin; no inhibition by Mg2+, Mn2+, Ca2+, Ba2+, NaCN, NaN3, sodium arsenite, p-hydroxymercuribenzoate; soybean trypsin inhibitor
-
additional information
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-
-
additional information
-
2-mercaptoethanol (Serratia marcescens); diisopropyl phosphofluoridate (Serratia marcescens); GSH, EGTA (Serratia marcescens), phosphoramidon, zincov (i.e. 2-(N-hydroxycarboxamido)-4-methylpentanoyl-L-Ala-glycinamide, thermolysin inhibitor); monoiodoacetic acid (Serratia marcescens)
-
additional information
-
IAA; PCMB
-
additional information
-
PCMB
-
additional information
-
not inhibited by iodoacetic acid and phenylmethylsulfonyl fluoride
-
additional information
-
not inhibitory: pepstatin (0.0015 mM), tosyllysyl chloromethyl ketone (0.05 mM), tosylphenylalanyl chloromethyl ketone (0.05 mM), tiorphan (0.004 mM), Triton X-100 and Tween up to 0.1% (v/v)
-