sameAs
P688
The Wilson disease protein ATP7B resides in the late endosomes with Rab7 and the Niemann-Pick C1 proteinCopper-induced trafficking of the cU-ATPases: a key mechanism for copper homeostasisThe distinct functional properties of the nucleotide-binding domain of ATP7B, the human copper-transporting ATPase: analysis of the Wilson disease mutations E1064A, H1069Q, R1151H, and C1104FMetallochaperone Atox1 transfers copper to the NH2-terminal domain of the Wilson's disease protein and regulates its catalytic activitySignals regulating trafficking of Menkes (MNK; ATP7A) copper-translocating P-type ATPase in polarized MDCK cellsCopper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B)Functional properties of the human copper-transporting ATPase ATP7B (the Wilson's disease protein) and regulation by metallochaperone Atox1Binding of copper(I) by the Wilson disease protein and its copper chaperoneATP7B mediates vesicular sequestration of copper: insight into biliary copper excretionCopper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7ASolution structure of the N-domain of Wilson disease protein: distinct nucleotide-binding environment and effects of disease mutationsThe Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease geneFunctional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.
P921
Q24293217-EB453114-82B8-4C3C-B494-B2E468A9EFDEQ24294303-DAE441B5-C4E8-41DE-9891-5210D120BDCEQ24297174-A04534D0-E69A-4F1F-9F47-431D2A9CDC18Q24298103-2DBD9FC5-C282-4E70-9D72-4D72197F74D5Q24299890-DF597AC9-3F06-41C6-9F55-2E2977DFD1BCQ24300903-D8F6769B-3FCE-4C6B-9D63-7483EDFD5C04Q24302394-2F0543AC-FFE8-4D72-A2D8-118AA9D21BBDQ24304146-E14C1658-EED0-4EB7-B33B-C275A4077070Q24304281-5FCA9343-A237-43DE-9444-73AB4045FE78Q24309611-A2938618-A748-4A4B-A34C-BE325C6455E5Q24310820-A9E43CE6-B6D2-411B-A43C-A34A880C79AFQ24336948-1347B38C-9808-485F-AA31-C24B6696DCD8Q28118944-DDD22F84-0504-4A72-8B73-9D37FBBBE3B5Q29346870-0159CFCB-B78B-4A8C-96D5-3A9DDF8F00E1
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in ATPase copper transporting beta
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
ATP-aza7B
@pl
ATP7B
@ca
ATP7B
@cy
ATP7B
@es
ATP7B
@pt
ATP7B
@pt-br
ATP7B
@ru
ATP7B
@uk
ATPase copper transporting beta
@en
ATPase copper transporting beta
@nl
type
label
ATP-aza7B
@pl
ATP7B
@ca
ATP7B
@cy
ATP7B
@es
ATP7B
@pt
ATP7B
@pt-br
ATP7B
@ru
ATP7B
@uk
ATPase copper transporting beta
@en
ATPase copper transporting beta
@nl
altLabel
ATP7B
@de
ATP7B
@en
ATP7B
@pl
ATPase, Cu(2+)- transporting, beta polypeptide
@en
ATPase, Cu++ transporting, beta polypeptide
@en
Gen de la malaltia de Wilson
@ca
Wilson disease-associated protein
@en
copper pump 2
@en
copper-transporting ATPase 2
@en
copper-transporting protein ATP7B
@en
prefLabel
ATP-aza7B
@pl
ATP7B
@ca
ATP7B
@cy
ATP7B
@es
ATP7B
@pt
ATP7B
@pt-br
ATP7B
@ru
ATP7B
@uk
ATPase copper transporting beta
@en
ATPase copper transporting beta
@nl
P361
P527
P637
P638
P680
P681
P682
P705
P352
P6366
P637
P646
P2888
P31
P352
P361
P527
P6366
2777614572
2910782815
P637
NP_001005918
NP_001230111
NP_001317507
NP_001317508
XP_005266480
XP_005266481
XP_005266487
XP_005266488
XP_006719900
P638
P646
/m/02qxkgm
P680
P681
P682
P702
P703
P705
ENSP00000242839
ENSP00000342559
ENSP00000383217
ENSP00000383221
ENSP00000393343
ENSP00000416738
ENSP00000489234
ENSP00000489398
ENSP00000489512
ENSP00000500964