Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Adenoma
Somatic mutations of the ATP1A1 gene and aldosterone-producing adenomas.
Cardiomegaly
Effect of chronic renal failure on cardiac contractile function, calcium cycling, and gene expression of proteins important for calcium homeostasis in the rat.
Cardiovascular Diseases
Digoxin and membrane sodium potassium ATPase inhibition in cardiovascular disease.
Cardiovascular Diseases
The physiological and clinical importance of sodium potassium ATPase in cardiovascular diseases.
Cystic Fibrosis
Changes in ion transport in inflammatory disease.
Cystic Fibrosis
Tear Production After Bilateral Main Lacrimal Gland Resection in Rabbits.
Diabetes Mellitus
Comparison of Serum Levels of Fructosamine and Erythrocyte Sodium Potassium ATPase (Na+/K+ ATPase) in Gestational Diabetes Mellitus (GDM) and non-Gestational Diabetes Mellitus (non GDM) Patients.
Diabetes Mellitus
[Disorders of sorbitol and myoinositol metabolism and the activity of sodium, potassium ATPase in the pathogenesis of peripheral neuropathy in patients with diabetes mellitus]
Diabetes, Gestational
Comparison of Serum Levels of Fructosamine and Erythrocyte Sodium Potassium ATPase (Na+/K+ ATPase) in Gestational Diabetes Mellitus (GDM) and non-Gestational Diabetes Mellitus (non GDM) Patients.
Epilepsy, Benign Neonatal
Genetics of the epilepsies.
Essential Hypertension
Raised sodium pump activity and a circulating sodium transport inhibitor demonstrated on red blood cells of patients with untreated essential hypertension: correlation of pump activity with potassium permeability.
Gastrointestinal Diseases
Inhibition of gastric H(+),K(+)-ATPase and Helicobacter pylori growth by phenolic antioxidants of Curcuma amada.
Herpes Simplex
Inhibitors of the sodium potassium ATPase that impair herpes simplex virus replication identified via a chemical screening approach.
Herpes Zoster
Endothelin-1 stimulation of aldosterone and zona glomerulosa ouabain-sensitive sodium/potassium-ATPase.
Hyperaldosteronism
Somatic mutations of the ATP1A1 gene and aldosterone-producing adenomas.
Hyperglycemia
Biological Activity of c-Peptide in Microvascular Complications of Type 1 Diabetes-Time for Translational Studies or Back to the Basics?
Hypertension
Effect of chronic renal failure on cardiac contractile function, calcium cycling, and gene expression of proteins important for calcium homeostasis in the rat.
Hypertension
Is the circulating ouabain-like compound ouabain?
Hypertension
Raised sodium pump activity and a circulating sodium transport inhibitor demonstrated on red blood cells of patients with untreated essential hypertension: correlation of pump activity with potassium permeability.
Hypertension
[Cellular bases of hypertension in pregnancy. V. Study of sodium, potassium ATPase in erythrocyte ghosts]
Infections
Inhibition of gastric H(+),K(+)-ATPase and Helicobacter pylori growth by phenolic antioxidants of Curcuma amada.
Migraine Disorders
Genetics of the epilepsies.
Migraine with Aura
Genetics of the epilepsies.
Peripheral Nervous System Diseases
[Disorders of sorbitol and myoinositol metabolism and the activity of sodium, potassium ATPase in the pathogenesis of peripheral neuropathy in patients with diabetes mellitus]
Polycystic Kidney Diseases
Ontogeny of dexamethasone binding and sodium potassium ATPase activity in experimental murine polycystic kidney disease.
Pre-Eclampsia
Role of endogenous digitalis-like factors in the clinical manifestations of severe preeclampsia: a sytematic review.
Pulmonary Edema
Role of nitric oxide metabolites in reduction of sodium potassium ATPase dependent pulmonary edema clearance.
Renal Insufficiency
Sodium potassium ATPase activity in human rectal mucosa with and without renal insufficiency.
Seizures
Genetics of the epilepsies.
Starvation
A chimeric Anabaena/ Escherichia coli KdpD protein (Anacoli KdpD) functionally interacts with E. coli KdpE and activates kdp expression in E. coli.
Stomach Ulcer
Inhibition of gastric H(+),K(+)-ATPase and Helicobacter pylori growth by phenolic antioxidants of Curcuma amada.
Tuberculosis
Interaction of the sensor module of Mycobacterium tuberculosis H37Rv KdpD with members of the Lpr family.
Tuberculosis
Role of the kdpDE Regulatory Operon of Mycobacterium tuberculosis in Modulating Bacterial Growth in vitro.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
122200
calculated from sequence of cDNA
128400
calculated from sequence of cDNA
129500
Udotea petiolata
-
calculated from sequence of cDNA
150600
-
DNA-sequence analysis
16000
-
SDS-PAGE, KdpCsol cleavage product
20000
-
1 * 59000 + 1 * 72000 + 1 * 20000 + 1 * 3000, SDS-PAGE
20267
-
1 * 58189 + 1 * 72112 + 1 * 20267, DNA-sequence analysis
23500
-
1 * 70000 + 1 * 43500 + 1 * 23500, SDS-PAGE
350000
-
gel filtration, KdpFABC complex, a cross-linked preparation
43500
-
1 * 70000 + 1 * 43500 + 1 * 23500, SDS-PAGE
47000
-
1 * 47000 + 1 * 90000 + 1 * 22000, SDS-PAGE
58189
-
1 * 58189 + 1 * 72112 + 1 * 20267, DNA-sequence analysis
70000
-
1 * 70000 + 1 * 43500 + 1 * 23500, SDS-PAGE
72112
-
1 * 58189 + 1 * 72112 + 1 * 20267, DNA-sequence analysis
90000
-
1 * 47000 + 1 * 90000 + 1 * 22000, SDS-PAGE
21000
-
1 * 59000 + 1 * 72000 + 1 * 21000, SDS-PAGE
21000
-
1 * 59000 + 1 * 72000 + 1 * 21000 + 1 * 4000-6000, SDS-PAGE
22000
-
1 * 79000 + 1 * 74000 + 1 * 22000, SDS-PAGE
22000
-
1 * 79000 + 1 * 74000 + 1 * 22000, SDS-PAGE
22000
-
1 * 47000 + 1 * 90000 + 1 * 22000, SDS-PAGE
59000
-
1 * 59000 + 1 * 72000 + 1 * 21000, SDS-PAGE
59000
-
1 * 59000 + 1 * 72000 + 1 * 21000 + 1 * 4000-6000, SDS-PAGE
59000
-
1 * 59000 + 1 * 72000 + 1 * 20000 + 1 * 3000, SDS-PAGE
72000
-
1 * 59000 + 1 * 72000 + 1 * 21000, SDS-PAGE
72000
-
1 * 59000 + 1 * 72000 + 1 * 21000 + 1 * 4000-6000, SDS-PAGE
72000
-
1 * 59000 + 1 * 72000 + 1 * 20000 + 1 * 3000, SDS-PAGE
72000
-
2 * 72000, SDS-PAGE, functional and structural dimeric enzyme with a close vicinity of two KdpB subunits within the functional KdpFABC complex, a dissociation constant for a monomer/dimer equilibrium between 30 and 50 nM, structure, overview
74000
-
1 * 79000 + 1 * 74000 + 1 * 22000, SDS-PAGE
74000
-
1 * 79000 + 1 * 74000 + 1 * 22000, SDS-PAGE
79000
-
1 * 79000 + 1 * 74000 + 1 * 22000, SDS-PAGE
79000
-
1 * 79000 + 1 * 74000 + 1 * 22000, SDS-PAGE
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
DELTAkdpX
-
truncation of the kdpX gene leads to a less efficient K+-pump than wild-type
DELTAkdpY
-
truncation of the kdpY gene has a significant impact on the growth of the Escherichia coli mutant TK2205, which is unable to grow at low potassium concentrations
DELTAkdpZ
-
truncation of the kdpZ gene has a significant impact on the growth of the Escherichia coli mutant TK2205, which is unable to grow at low potassium concentrations
DELTAkdpZY
-
loss of K+ transport
A220F
-
lower affinity to K+ than wild-type
A220K
-
lower affinity to K+ than wild-type
A220P
-
lower affinity to K+ than wild-type
A220S
-
lower affinity to K+ than wild-type
A220Y
-
lower affinity to K+ than wild-type
A224H
-
lower affinity to K+ than wild-type
A224K
-
lower affinity to K+ than wild-type
A224Q
-
lower affinity to K+ than wild-type
A341K
-
lower affinity to K+ than wild-type
A342K
-
lower affinity to K+ than wild-type
A346K
-
lower affinity to K+ than wild-type
A346Y
-
lower affinity to K+ than wild-type
A459K
-
lower affinity to K+ than wild-type
A464H
-
lower affinity to K+ than wild-type
A464K
-
lower affinity to K+ than wild-type
A464L
-
lower affinity to K+ than wild-type
A464P
-
lower affinity to K+ than wild-type
A464Y
-
lower affinity to K+ than wild-type
C344K
-
lower affinity to K+ than wild-type
C344P
-
lower affinity to K+ than wild-type
D352K
-
lower affinity to K+ than wild-type
E223K
-
lower affinity to K+ than wild-type
E223P
-
lower affinity to K+ than wild-type
F235K
-
lower affinity to K+ than wild-type
F236K
-
lower affinity to K+ than wild-type
F335K
-
lower affinity to K+ than wild-type
F354G
-
lower affinity to K+ than wild-type
F471E
-
lower affinity to K+ than wild-type
F471K
-
lower affinity to K+ than wild-type
F471P
-
lower affinity to K+ than wild-type
F471Y
-
lower affinity to K+ than wild-type
G120K
-
lower affinity to K+ than wild-type
G217A
-
lower affinity to K+ than wild-type
G217K
-
lower affinity to K+ than wild-type
G229H
-
lower affinity to K+ than wild-type
G229K
-
lower affinity to K+ than wild-type
G232A
-
lower affinity to K+ than wild-type
G232C
-
lower affinity to K+ than wild-type
G232E
-
lower affinity to K+ than wild-type
G232H
-
lower affinity to K+ than wild-type
G232K
-
lower affinity to K+ than wild-type
G232L
-
lower affinity to K+ than wild-type
G232P
-
lower affinity to K+ than wild-type
G232Q
-
lower affinity to K+ than wild-type
G232S
-
lower affinity to K+ than wild-type
G232Y
-
lower affinity to K+ than wild-type
G233E
-
lower affinity to K+ than wild-type
G233K
-
lower affinity to K+ than wild-type
G233P
-
lower affinity to K+ than wild-type
G233Q
-
lower affinity to K+ than wild-type
G233Y
-
lower affinity to K+ than wild-type
G234K
-
lower affinity to K+ than wild-type
G234P
-
lower affinity to K+ than wild-type
G358K
-
lower affinity to K+ than wild-type
G468K
-
lower affinity to K+ than wild-type
I225K
-
lower affinity to K+ than wild-type
I348C
-
lower affinity to K+ than wild-type
I348F
-
lower affinity to K+ than wild-type
I348K
-
lower affinity to K+ than wild-type
I348P
-
lower affinity to K+ than wild-type
I348Y
-
lower affinity to K+ than wild-type
I367K
-
lower affinity to K+ than wild-type
K226P
-
lower affinity to K+ than wild-type
L228K
-
lower affinity to K+ than wild-type
L330K
-
lower affinity to K+ than wild-type
L365K
-
lower affinity to K+ than wild-type
M366K
-
lower affinity to K+ than wild-type
N112K
-
lower affinity to K+ than wild-type
N112P
-
lower affinity to K+ than wild-type
N114E
-
lower affinity to K+ than wild-type
N114F
-
lower affinity to K+ than wild-type
N114H
-
lower affinity to K+ than wild-type
N114K
-
lower affinity to K+ than wild-type
N114L
-
lower affinity to K+ than wild-type
N114P
-
lower affinity to K+ than wild-type
N114Q
-
lower affinity to K+ than wild-type
N114S
-
lower affinity to K+ than wild-type
N114Y
-
lower affinity to K+ than wild-type
N231K
-
lower affinity to K+ than wild-type
N231P
-
lower affinity to K+ than wild-type
N231Y
-
lower affinity to K+ than wild-type
N237K
-
lower affinity to K+ than wild-type
N239H
-
lower affinity to K+ than wild-type
N239K
-
lower affinity to K+ than wild-type
N465K
-
lower affinity to K+ than wild-type
N466K
-
lower affinity to K+ than wild-type
N467K
-
lower affinity to K+ than wild-type
P362K
-
lower affinity to K+ than wild-type
Q116H
-
lower affinity to K+ than wild-type
Q116K
-
lower affinity to K+ than wild-type
Q116P
-
lower affinity to K+ than wild-type
Q116R
-
mutant with reduced affinity for K+
Q140A
-
site-directed mutagenesis, the mutant is still able to tolerate extreme potassium limitations below 0.1 mM, but shows 38% reduced growth compared to the wild-type
Q140A/R143A/V144A/A145S/A147S/R148A/L150A
-
site-directed mutagenesis of the complete 140-QIPRVAKARNL-150 ATP binding motif in KdpC, the mutant cells comprising a complete exchange of the signature motif show no growth if the potassium concentration drops below 5 mM
Q140E
-
site-directed mutagenesis, the mutant is still able to tolerate extreme potassium limitations below 0.1 mM, but shows 38% reduced growth compared to the wild-type
Q140N
-
site-directed mutagenesis, the mutant is still able to tolerate extreme potassium limitations below 0.1 mM, but shows 12% reduced growth compared to the wild-type
Q222K
-
lower affinity to K+ than wild-type
S119K
-
lower affinity to K+ than wild-type
S221K
-
lower affinity to K+ than wild-type
S343F
-
lower affinity to K+ than wild-type
S343K
-
lower affinity to K+ than wild-type
S343L
-
lower affinity to K+ than wild-type
S343Y
-
lower affinity to K+ than wild-type
S461F
-
lower affinity to K+ than wild-type
S461K
-
lower affinity to K+ than wild-type
S461Y
-
lower affinity to K+ than wild-type
S469G
-
lower affinity to K+ than wild-type
S469H
-
lower affinity to K+ than wild-type
S469K
-
lower affinity to K+ than wild-type
S469L
-
lower affinity to K+ than wild-type
S469P
-
lower affinity to K+ than wild-type
S469Q
-
lower affinity to K+ than wild-type
S469Y
-
lower affinity to K+ than wild-type
T111G
-
lower affinity to K+ than wild-type
T111K
-
lower affinity to K+ than wild-type
T113F
-
lower affinity to K+ than wild-type
T113K
-
lower affinity to K+ than wild-type
T113P
-
lower affinity to K+ than wild-type
T113Y
-
lower affinity to K+ than wild-type
T230K
-
lower affinity to K+ than wild-type
T230Y
-
lower affinity to K+ than wild-type
T339H
-
lower affinity to K+ than wild-type
T339K
-
lower affinity to K+ than wild-type
T339Q
-
lower affinity to K+ than wild-type
T340F
-
lower affinity to K+ than wild-type
T340K
-
lower affinity to K+ than wild-type
T340Y
-
lower affinity to K+ than wild-type
T355A
-
lower affinity to K+ than wild-type
T355K
-
lower affinity to K+ than wild-type
V110K
-
lower affinity to K+ than wild-type
V331K
-
lower affinity to K+ than wild-type
V337K
-
lower affinity to K+ than wild-type
W115K
-
lower affinity to K+ than wild-type
Y458K
-
lower affinity to K+ than wild-type
Q116R
-
mutant with reduced affinity for K+
-
additional information
-
the 140-QIPRVAKARNL-150 ATP binding motif in KdpC is deleted completely, resulting in mutant DELTAQ-L, cells comprising a deletion of the signature motif showed no growth if the potassium concentration drops below 5 mM. The mutations generated result in different phenotypes with respect to tolerance of potassium limitation, overview
additional information
-
expression of plasmid-encoded kdpFABCcat3 is sufficient to complement the phenotype of a chromosomal kdpFABCcat3 deletion strain, whereas expression of only kdpFABC is not
additional information
-
expression of plasmid-encoded kdpFABCcat3 is sufficient to complement the phenotype of a chromosomal kdpFABCcat3 deletion strain, whereas expression of only kdpFABC is not
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Harvey, W.R.; Cioffi, M.; Dow, J.A.T.; Wolfersberger, M.G.
Potassium ion transport ATPase in insect epithelia
J. Exp. Biol.
106
91-117
1983
Schistocerca gregaria, Jamaicana flava, Locusta migratoria, Manduca sexta
brenda
Siebers, A.; Altendorf, K.
The K+-translocating Kdp-ATPase from Escherichia coli. Purification, enzymatic properties and production of complex- and subunit-specific antisera
Eur. J. Biochem.
178
131-140
1988
Escherichia coli, Escherichia coli TKA 1000
brenda
Hafer, J.; Siebers, A.; Bakker, E.P.
The high-affinity K+-translocating ATPase complex from Bacillus acidocaldarius consists of three subunits
Mol. Microbiol.
3
487-495
1989
Alicyclobacillus acidocaldarius
brenda
Siebers, A.; Altendorf, K.
Characterization of the phosphorylated intermediate of the K+-translocating Kdp-ATPase from Escherichia coli
J. Biol. Chem.
264
5831-5838
1989
Escherichia coli, Escherichia coli TKA 1000
brenda
Siebers, A.; Kollmann, R.; Dierkes, G.; Altendorf, K.
Rapid, high yield purification and characterization of the K+-translocating Kdp-ATPase from Escherichia coli
J. Biol. Chem.
257
12717-12721
1992
Escherichia coli, Escherichia coli TKA 1000
-
brenda
Abee, T.; Siebers, A.; Altendorf, K.; Konings, W.N.
Isolation and characterization of the high-affinity K+-translocating ATPase from Rhodobacter sphaeroides
J. Bacteriol.
174
6911-6917
1992
Cereibacter sphaeroides
brenda
Epstein, W.; Wieczorek, L.; Siebers, A.; Altendorf, K.
Potassium transport in Escherichia coli: genetic and biochemical characterization of the K+-transporting ATPase
Biochem. Soc. Trans.
12
235-236
1984
Escherichia coli
brenda
Kollmann, R.; Altendorf, K.
ATP-driven potassium transport in right-side-out membrane vesicles via the Kdp system of Escherichia coli
Biochim. Biophys. Acta
1143
62-66
1993
Escherichia coli, Escherichia coli TKA 1000
brenda
Fendler, K.; Drse, S.; Altendorf, K.; Bamberg, E.
Electrogenic K+ transport by the Kdp-ATPase of Escherichia coli
Biochemistry
35
8009-8017
1996
Escherichia coli, Escherichia coli TKA 1000
brenda
Iwane, A.H.; Ikeda, I.; Kimura, Y.; Fujiyoshi, Y.; Altendorf, K.; Epstein, W.
Two-dimensional crystals of the Kdp-ATPase of Escherichia coli
FEBS Lett.
396
172-176
1996
Escherichia coli, Escherichia coli TK 2242/pSR5
brenda
Gael, M.; Mllenkamp, T.; Puppe, W.; Altendorf, K.
The KdpF subunit is part of the K+-translocating Kdp complex of Escherichia coli and is responsible for stabilization of the complex in vitro
J. Biol. Chem.
274
37901-37907
1999
Escherichia coli, Escherichia coli TKW3205/pSR5
brenda
Fendler, K.; Drse, S.; Epstein, W.; Bamberg, E.; Altendorf, K.
The Kdp-ATPase of Escherichia coli mediates an ATP-dependent, K+-independent electrogenic partial reaction
Biochemistry
38
1850-1856
1999
Escherichia coli, Escherichia coli TKA 1000
brenda
Durell, S.R.; Bakker, E.P.; Guy, H.R.
Does the KdpA subunit from the high affinity K+-translocating P-type KDP-ATPase have a structure similar to that of K+ channels?
Biophys. J.
78
188-199
2000
Mycobacterium tuberculosis, Clostridium acetobutylicum (O32327), Escherichia coli (P03959), Synechocystis sp. PCC 6803 (P73866), Alicyclobacillus acidocaldarius (Q9XE11)
brenda
Behrens, M.; Schreiber, W.; Durre, P.
The high-affinity K-translocating ATPase complex from Clostridium acetobutylicum consists of six subunits
Anaerobe
7
159-169
2001
Clostridium acetobutylicum
-
brenda
Sebestian, J.; Petrmichlova, Z.; Sebestianova, S.; Naprstek, J.; Svobodova, J.
Osmoregulation in Bacillus subtilis under potassium limitation: a new inducible K+-stimulated, VO4(3-)-inhibited ATPase
Can. J. Microbiol.
47
1116-1125
2001
Bacillus subtilis
brenda
Gassel, M.; Altendorf, K.
Analysis of KdpC of the K+ -transporting KdpFABC complex of Escherichia coli
Eur. J. Biochem.
268
1772-1781
2001
Escherichia coli
brenda
Sardesai, A.A.; Gowrishankar, J.
Improvement in K+-limited growth rate associated with expression of the N-terminal fragment of one subunit (KdpA) of the multisubunit Kdp transporter in Escherichia coli
J. Bacteriol.
183
3515-3520
2001
Escherichia coli
brenda
Dorus, S.; Mimura, H.; Epstein, W.
Substrate-binding clusters of the K+-transporting Kdp ATPase of Escherichia coli investigated by amber suppression scanning mutagenesis
J. Biol. Chem.
276
9590-9598
2001
Escherichia coli
brenda
Ahnert, F.; Schmid, R.; Altendorf, K.; Greie, J.C.
ATP binding properties of the soluble part of the KdpC subunit from the Escherichia coli K(+)-transporting KdpFABC P-type ATPase
Biochemistry
45
11038-11046
2006
Escherichia coli
brenda
De Hertogh, B.; Lantin, A.; Baret, P.V.; Goffeau, A.
The Archaeal P-Type ATPases
J. Bioenerg. Biomembr.
36
135-142
2004
Halobacterium sp., Ferroplasma acidarmanus, Thermoplasma acidophilum (P57700), Thermoplasma volcanium (Q97BF6)
brenda
Barrero-Gil, J.; Garciadeblas, B.; Benito, B.
Sodium, potassium-atpases in algae and oomycetes
J. Bioenerg. Biomembr.
37
269-278
2005
Udotea petiolata, Pythium aphanidermatum (Q4LB39), Neopyropia yezoensis (Q4LB57), Pythium aphanidermatum 356128 (Q4LB39)
brenda
Heitkamp, T.; Kalinowski, R.; Boettcher, B.; Boersch, M.; Altendorf, K.; Greie, J.
K+-translocating KdpFABC P-type ATPase from Escherichia coli acts as a functional and structural dimer
Biochemistry
47
3564-3575
2008
Escherichia coli
brenda
Vagabov, V.M.; Ivanov, A.Y.; Kulakovskaya, T.V.; Kulakovskaya, E.V.; Petrov, V.V.; Kulaev, I.S.
Efflux of potassium ions from cells and spheroplasts of Saccharomyces cerevisiae yeast treated with silver and copper ions
Biochemistry (Moscow)
73
1224-1227
2008
Saccharomyces cerevisiae, Saccharomyces cerevisiae VKM Y-1173
brenda
Strahl, H.; Greie, J.C.
The extremely halophilic archaeon Halobacterium salinarum R1 responds to potassium limitation by expression of the K+-transporting KdpFABC P-type ATPase and by a decrease in intracellular K+
Extremophiles
12
741-752
2008
Halobacterium salinarum, Halobacterium salinarum R1
brenda
Irzik, K.; Pfroetzschner, J.; Goss, T.; Ahnert, F.; Haupt, M.; Greie, J.C.
The KdpC subunit of the Escherichia coli K+-transporting KdpB P-type ATPase acts as a catalytic chaperone
FEBS J.
278
3041-3053
2011
Escherichia coli
brenda
Stock, C.; Hielkema, L.; Tascon, I.; Wunnicke, D.; Oostergetel, G.; Azkargorta, M.; Paulino, C.; Haenelt, I.
Cryo-EM structures of KdpFABC suggest a K+ transport mechanism via two inter-subunit half-channels
Nat. Commun.
9
4971
2018
Escherichia coli (P03959 and P03960 and P03961 and P36937)
brenda
Dani, P.; Ujaoney, A.K.; Apte, S.K.; Basu, B.
Regulation of potassium dependent ATPase (kdp) operon of Deinococcus radiodurans
PLoS ONE
12
e0188998
2017
Deinococcus radiodurans (Q9RZN7 and Q9RZP0 and Q9RZN6), Deinococcus radiodurans DSM 20539 (Q9RZN7 and Q9RZP0 and Q9RZN6)
brenda