Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 7.2.2.9 extracted from

  • Pilankatta, R.; Lewis, D.; Adams, C.M.; Inesi, G.
    High yield heterologous expression of wild-type and mutant Cu+-ATPase (ATP7B, Wilson disease protein) for functional characterization of catalytic activity and serine residues undergoing copper-dependent phosphorylation (2009), J. Biol. Chem., 284, 21307-21316.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

Cloned (Comment) Organism
expression of wild-type and mutant myc-tagged ATP7Bs in COS1 cells using an adenoviral vector Homo sapiens

Protein Variants

Protein Variants Comment Organism
C983A/C985A site-directed mutagenesis of CXC copper binding motif in the transmembrane copper site TM6, absence of alkali labile phosphoenzyme formation Homo sapiens
D1027N site-directed mutagenesis of the P domain, absence of alkali labile phosphoenzyme formation Homo sapiens

Inhibitors

Inhibitors Comment Organism Structure
Bathocuproine disulfonate a copper chelator, reduced ATP7B activity Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
microsome
-
Homo sapiens
-
-

Metals/Ions

Metals/Ions Comment Organism Structure
Mg2+ required Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
ATP + H2O + Cu2+/in Homo sapiens
-
ADP + phosphate + Cu2+/out
-
?

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Posttranslational Modification

Posttranslational Modification Comment Organism
phosphoprotein ATP7B phosphorylation with ATP occurs with diphasic kinetics and is totally copper-dependent Homo sapiens

Purification (Commentary)

Purification (Comment) Organism
recombinant myc-tagged ATP7B is isolated from the microsomal fraction of COS-1 cell homogenates Homo sapiens

Specific Activity [micromol/min/mg]

Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
0.081
-
partially purifed recombinant ATP7B in microsomes, copper-dependent, steady-state ATPase, 37°C, pH 6.0, in presence of copper and copper chelator Homo sapiens
0.112
-
partially purifed recombinant ATP7B in microsomes, copper-dependent, steady-state ATPase, 37°C, pH 6.0 in presence of copper Homo sapiens

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
ATP + H2O + Cu2+/in
-
Homo sapiens ADP + phosphate + Cu2+/out
-
?
ATP + H2O + Cu2+/in ATP7B phosphorylation with ATP occurs with diphasic kinetics and is totally copper-dependent Homo sapiens ADP + phosphate + Cu2+/out
-
?

Synonyms

Synonyms Comment Organism
ATP7B
-
Homo sapiens
Cu+-ATPase
-
Homo sapiens
Wilson disease protein
-
Homo sapiens

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Homo sapiens

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
6
-
assay at Homo sapiens

General Information

General Information Comment Organism
physiological function ATP7B is a P-type ATPase required for copper homeostasis and related to Wilson disease of humans Homo sapiens