EC Number | Application | Comment | Organism |
---|---|---|---|
3.4.11.7 | drug development | development of potent and selective APA inhibitors crossing the blood-brain barrier after oral administration for use as centrally-acting antihypertensive agents | Mus musculus |
EC Number | Cloned (Comment) | Organism |
---|---|---|
3.4.11.7 | recombinant expression of His-tagged wild-type and mutant enzymes in CHO-K1 cells | Mus musculus |
EC Number | Protein Variants | Comment | Organism |
---|---|---|---|
3.4.11.7 | additional information | Ca2+ activation profile of purified recombinant wild-type and mutated His-mAPAs, using an acidic substrate alpha-L-glutamyl-beta-naphthylamide, overview | Mus musculus |
3.4.11.7 | R878A | site-directed mutagenesis, the mutant shows decreased affinity for the acidic substrate, alpha-L-glutamyl-beta-naphthylamide, with a slight decrease in substrate hydrolysis velocity either with or without Ca2+ compared to the wild-type enzyme. Analysis of the 3D models of the Arg878 mutated APAs reveals a change in the volume of the S1 subsite, which may impair the binding and/or the optimal positioning of the substrate in the active site as well as its hydrolysis | Mus musculus |
3.4.11.7 | R878K | site-directed mutagenesis, the mutant shows decreased affinity for the acidic substrate, alpha-L-glutamyl-beta-naphthylamide, with a slight decrease in substrate hydrolysis velocity either with or without Ca2+ compared to the wild-type enzyme. Analysis of the 3D models of the Arg878 mutated APAs reveals a change in the volume of the S1 subsite, which may impair the binding and/or the optimal positioning of the substrate in the active site as well as its hydrolysis | Mus musculus |
EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
3.4.11.7 | (4R)-4-amino-5-sulfanylpentanoic acid | a linear competitive inhibitor | Mus musculus | |
3.4.11.7 | (S)-3-amino-4-mercapto-butyl sulfonic acid | i.e. EC33, a selective APA inhibitor, docking analysis in the presence of Ca2+, the ligand interacts with S1 subsite of Arg-878 in murine APA, three-dimensional structure modelling reavealing a change in the volume of the S1 subsite, which may impair the binding and/or the optimal positioning of the substrate in the active site as well as its hydrolysis, overview | Mus musculus | |
3.4.11.7 | 2,6-diaminohexane-1-thiol | a linear competitive inhibitor | Mus musculus | |
3.4.11.7 | 4-amino-4-phosphonobutyric acid | a specific and selective APA inhibitor, a linear competitive inhibitor | Mus musculus | |
3.4.11.7 | methionine-thiol | a linear competitive inhibitor | Mus musculus | |
3.4.11.7 | additional information | ligand docking study and molecular dynamics simulations with wild-type and mutant enzymes, overview | Mus musculus |
EC Number | KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
3.4.11.7 | additional information | - |
additional information | Michaelis-Menten kinetics | Mus musculus | |
3.4.11.7 | 0.0391 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.165 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme | Mus musculus | |
3.4.11.7 | 0.221 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.269 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 1.5 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 12.5 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
3.4.11.7 | membrane | membrane-bound | Mus musculus | 16020 | - |
EC Number | Metals/Ions | Comment | Organism | Structure |
---|---|---|---|---|
3.4.11.7 | Ca2+ | localized at the bottom of the S1 subsite, activates the enzyme and plays a key role of Arg878 together with Ca2 + in APA substrate specificity for N-terminal acidic amino acid residues by ensuring the optimal positioning of acidic substrates during catalysis. The Ca2+ atom interacts with the acidic side chains of Asp213 and Asp218, the carbonyl group of Glu215 and three water molecules, one of them being engaged in a hydrogen bond with the negatively charged carboxylate side chains of the inhibitors. Ca2+ activation profile of purified recombinant wild-type and mutated His-mAPAs, using an acidic substrate alpha-L-glutamyl-beta-naphthylamide, overview. Enzyme residue Arg878 does not contribute to Ca2+ binding in the S1 subsite | Mus musculus | |
3.4.11.7 | Zn2+ | a zinc metalloprotease, Zn2+ atom is coordinated by the two histidine residues, His385 and His389, of the HEXXH motif, a water molecule, Glu408 of the WLNEG motif and either by one of the oxygen atoms of the phosphate of GluPO3H2, three-dimensional structure modelling | Mus musculus |
EC Number | Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|---|
3.4.11.7 | 160000 | - |
- |
Mus musculus |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.4.11.7 | angiotensin II + H2O | Mus musculus | - |
angiotensin III + L-Asp | - |
? | |
3.4.11.7 | cholecystokinin-8 + H2O | Mus musculus | - |
? | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
3.4.11.7 | Mus musculus | P16406 | - |
- |
EC Number | Purification (Comment) | Organism |
---|---|---|
3.4.11.7 | recombinant His-tagged wild-type and mutant enzymes from CHO-K1 cells by Co2+ affinity chromatography | Mus musculus |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
3.4.11.7 | brain | - |
Mus musculus | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.4.11.7 | alpha-L-aspartate-beta-naphthylamide + H2O | high activity | Mus musculus | L-aspartate + beta-naphthylamine | - |
? | |
3.4.11.7 | alpha-L-glutamyl-beta-naphthylamide + H2O | best substrate | Mus musculus | L-glutamine + beta-naphthylamine | - |
? | |
3.4.11.7 | angiotensin II + H2O | - |
Mus musculus | angiotensin III + L-Asp | - |
? | |
3.4.11.7 | cholecystokinin-8 + H2O | - |
Mus musculus | ? | - |
? | |
3.4.11.7 | L-alanine-beta-naphthylamide + H2O | low activity | Mus musculus | L-alanine + beta-naphthylamine | - |
? | |
3.4.11.7 | L-lysine-beta-naphthylamide + H2O | low activity | Mus musculus | L-lysine + beta-naphthylamine | - |
? | |
3.4.11.7 | additional information | enzyme APA cleaves the N-terminal glutamyl or aspartyl residue from peptide substrates | Mus musculus | ? | - |
? |
EC Number | Subunits | Comment | Organism |
---|---|---|---|
3.4.11.7 | homodimer | 2 * 80000 | Mus musculus |
3.4.11.7 | More | aminopeptidase A (APA) is a 160 kDa homodimeric type II Zn2+ membrane-bound aminopeptidase | Mus musculus |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
3.4.11.7 | aminopeptidase A | - |
Mus musculus |
3.4.11.7 | APA | - |
Mus musculus |
3.4.11.7 | ENPEP | - |
Mus musculus |
3.4.11.7 | mAPA | - |
Mus musculus |
3.4.11.7 | type II Zn2+ membrane-bound aminopeptidase | - |
Mus musculus |
EC Number | Turnover Number Minimum [1/s] | Turnover Number Maximum [1/s] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
3.4.11.7 | 3.12 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus | |
3.4.11.7 | 4.95 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 13.9 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme | Mus musculus | |
3.4.11.7 | 22.4 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 81.7 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 135 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K, with 4 mM Ca2+ | Mus musculus |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
3.4.11.7 | 7.4 | - |
assay at | Mus musculus |
EC Number | Ki Value [mM] | Ki Value maximum [mM] | Inhibitor | Comment | Organism | Structure |
---|---|---|---|---|---|---|
3.4.11.7 | 0.000074 | - |
4-amino-4-phosphonobutyric acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.000118 | - |
2,6-diaminohexane-1-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 0.000268 | - |
(S)-3-amino-4-mercapto-butyl sulfonic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.000314 | - |
(4R)-4-amino-5-sulfanylpentanoic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.000317 | - |
2,6-diaminohexane-1-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme | Mus musculus | |
3.4.11.7 | 0.000378 | - |
2,6-diaminohexane-1-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus | |
3.4.11.7 | 0.000475 | - |
methionine-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 0.000619 | - |
4-amino-4-phosphonobutyric acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.00075 | - |
methionine-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme | Mus musculus | |
3.4.11.7 | 0.00125 | - |
methionine-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus | |
3.4.11.7 | 0.00152 | - |
(S)-3-amino-4-mercapto-butyl sulfonic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.00157 | - |
(4R)-4-amino-5-sulfanylpentanoic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme | Mus musculus | |
3.4.11.7 | 0.00172 | - |
(4R)-4-amino-5-sulfanylpentanoic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 0.002 | - |
(S)-3-amino-4-mercapto-butyl sulfonic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.00322 | - |
methionine-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 0.00514 | - |
methionine-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus | |
3.4.11.7 | 0.0065 | - |
4-amino-4-phosphonobutyric acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.00751 | - |
2,6-diaminohexane-1-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.00918 | - |
methionine-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.01 | - |
(4R)-4-amino-5-sulfanylpentanoic acid | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus | |
3.4.11.7 | 0.0134 | - |
2,6-diaminohexane-1-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 0.0139 | - |
2,6-diaminohexane-1-thiol | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K, with 4 mM Ca2+ | Mus musculus |
EC Number | General Information | Comment | Organism |
---|---|---|---|
3.4.11.7 | malfunction | mutagenic replacement of Arg-878 with an alanine or a lysine residue decreases the affinity of the recombinant enzymes for the acidic substrate, alpha-L-glutamyl-beta-naphthylamide, with a slight decrease in substrate hydrolysis velocity either with or without Ca2+. In the absence of Ca2+, the mutations modify the substrate specificity of enzyme APA for the acidic substrate. The mutated enzymes hydrolyse more efficiently basic and neutral substrates, although the addition of Ca2+ partially restores the acidic substrate specificity | Mus musculus |
3.4.11.7 | additional information | residue Arg878 together with Ca2+ is responsible in mouse aminopeptidase A for the substrate specificity for N-terminal acidic amino-acid residues by ensuring the optimal positioning of acidic substrates during catalysis. Docking and molecular dynamics simulations using the crystal structure of human aminopeptidase A complexed with Glu and Ca2+, PDB ID 4KXD, overview | Mus musculus |
3.4.11.7 | physiological function | aminopeptidase A (APA) is a membrane-bound zinc metalloprotease cleaving, in the brain, the N-terminal aspartyl residue of angiotensin II to generate angiotensin III, which exerts a tonic stimulatory effect on the control of blood pressure in hypertensive animals | Mus musculus |
EC Number | kcat/KM Value [1/mMs-1] | kcat/KM Value Maximum [1/mMs-1] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|---|
3.4.11.7 | 0.3 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K | Mus musculus | |
3.4.11.7 | 3.3 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A | Mus musculus | |
3.4.11.7 | 84.3 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme | Mus musculus | |
3.4.11.7 | 102 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878A, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 502 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged mutant R878K, with 4 mM Ca2+ | Mus musculus | |
3.4.11.7 | 2090 | - |
alpha-L-glutamyl-beta-naphthylamide | pH 7.4, temperature not specified in the publication, recombinant His-tagged wild-type enzyme, with 4 mM Ca2+ | Mus musculus |