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searching for ATPase 323 found (1581 total)

alternate case: aTPase

Sodium-calcium exchanger (2,223 words) [view diff] exact match in snippet view article find links to article

transmembrane pump that exports calcium from the cell is the plasma membrane Ca2+ ATPase (PMCA), which has a much higher affinity but a much lower capacity. Since

Probable cation-transporting ATPase 13A2 is an enzyme that in humans is encoded by the ATP13A2 gene that is involved in the transport of divalent transition

P-type H+-exporting transporter * EC 7.1.2.2: H+-transporting two-sector ATPase * * No Wikipedia article EC 7.1.3.1: H+-exporting diphosphatase * EC 7.1

cell death. Bafilomycin A1 specifically targets the vacuolar-type H+ -ATPase (V-ATPase) enzyme, a membrane-spanning proton pump that acidifies either the

Probable cation-transporting ATPase 13A3 is an enzyme that in humans is encoded by the ATP13A3 gene. GRCh38: Ensembl release 89: ENSG00000133657 – Ensembl

decrease its rate of contractions by inhibiting the cellular sodium-potassium ATPase pump. Their beneficial medical uses include treatments for congestive heart

N-terminal ATPase domain of gyrase and yeast topoisomerase II have been solved in complex with AMPPNP (an ATP analogue), showing that two ATPase domains

AAA (ATPases Associated with diverse cellular Activities) proteins (speak: tripple-A ATPases) are a large group of protein family sharing a common conserved

active transport into the stomach. The enzyme hydrogen potassium ATPase (H+/K+ ATPase) is unique to the parietal cells and transports the H+ against a

Proton pump inhibitors (PPIs) block the gastric hydrogen potassium ATPase (H+/K+ ATPase) and inhibit gastric acid secretion. These drugs have emerged as

proton ATPase 21 kDa proteolipid subunit is an enzyme that in humans is encoded by the ATP6V0B gene. This gene encodes a component of vacuolar ATPase (V-ATPase)

Proton pump inhibitors (PPIs) block the gastric hydrogen potassium ATPase (H+/K+ ATPase) and inhibit gastric acid secretion. These drugs have emerged as

proton ATPase 116 kDa subunit a isoform 1 is an enzyme that in humans is encoded by the ATP6V0A1 gene. This gene encodes a component of vacuolar ATPase (V-ATPase)

organelles. Vacuolar ATPase (V-ATPase) is composed of a cytosolic, V1, (site of the ATP catalytic site) and a transmembrane, V0, domain. V-ATPase dependent organelle

microtubule-severing ATPase EC 5.6.1.2: dynein ATPase EC 5.6.1.3: plus-end-directed kinesin ATPase EC 5.6.1.4: minus-end-directed kinesin ATPase EC 5.6.1.5: proteasome

proton ATPase subunit B, brain isoform is an enzyme that in humans is encoded by the ATP6V1B2 gene. This gene encodes a component of vacuolar ATPase (V-ATPase)

proton ATPase catalytic subunit A is an enzyme that in humans is encoded by the ATP6V1A gene. This gene encodes a component of vacuolar ATPase (V-ATPase),

Probable phospholipid-transporting ATPase IIA is a protein that in humans is encoded by the ATP9A gene. GRCh38: Ensembl release 89: ENSG00000054793 – Ensembl

proton ATPase subunit D is an enzyme that in humans is encoded by the ATP6V1D gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

proton ATPase subunit C 1 is an enzyme that in humans is encoded by the ATP6V1C1 gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

THE ATPASE ACTIVE SITE 1hx1: CRYSTAL STRUCTURE OF A BAG DOMAIN IN COMPLEX WITH THE HSC70 ATPASE DOMAIN 1kax: 70KD HEAT SHOCK COGNATE PROTEIN ATPASE DOMAIN

many leaderless mRNAs probably initiated by scanning. The process of ABCE1 ATPase-based recycling is also shared with eukaryotes. Being a prokaryote without

proton ATPase subunit B, kidney isoform is an enzyme that in humans is encoded by the ATP6V1B1 gene. This gene encodes a component of vacuolar ATPase (V-ATPase)

proton ATPase subunit G 1 is an enzyme that in humans is encoded by the ATP6V1G1 gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

show that this particle is correlated with ATPase activity in uncoupled mitochondria and with the ATPase activity in submitochondrial particles created

proton ATPase subunit C 2 is an enzyme that in humans is encoded by the ATP6V1C2 gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

Cardenolides are toxic to animals through inhibition of the enzyme Na+/K+‐ATPase, which is responsible for maintaining the sodium and potassium ion gradients

1016/S0163-4453(05)80037-4. PMID 1602151. Ohta S, Kagawa Y (1986). "Human F1-ATPase: molecular cloning of cDNA for the beta subunit". J. Biochem. 99 (1): 135–41

Leslie AG, Lutter R, Walker JE (1994). "Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria". Nature. 370 (6491): 621–8. Bibcode:1994Natur

proton ATPase subunit G 2 is an enzyme that in humans is encoded by the ATP6V1G2 gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

channel-conductance-controlling ATPase - chaperone protein - chlordecone reductase - chloroplast protein-transporting ATPase - cholestanetriol 26-monooxygenase

proton ATPase subunit F is an enzyme that in humans is encoded by the ATP6V1F gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

instance, ATPase fiber type is related to contraction speed, because high ATPase activity allows faster crossbridge cycling. While ATPase activity is

26S protease regulatory subunit 6A, also known as 26S proteasome AAA-ATPase subunit Rpt5, is an enzyme that in humans is encoded by the PSMC3 gene. This

26S protease regulatory subunit 7, also known as 26S proteasome AAA-ATPase subunit Rpt1, is an enzyme that in humans is encoded by the PSMC2 gene This

proton ATPase subunit d 1 is an enzyme that in humans is encoded by the ATP6V0D1 gene. This gene encodes a component of vacuolar ATPase (V-ATPase), a multisubunit

proton ATPase 116 kDa subunit a isoform 4 is an enzyme that in humans is encoded by the ATP6V0A4 gene. This gene encodes a component of vacuolar ATPase (V-ATPase)

V-type proton ATPase subunit E 2 is an enzyme that in humans is encoded by the ATP6V1E2 gene. GRCh38: Ensembl release 89: ENSG00000250565 – Ensembl, May

Ca2+-ATPase (SERCA2) which transports calcium from cytosol into the sarcoplasmic reticulum. When phosphorylated (by PKA) - disinhibition of Ca2+-ATPase of

26S protease regulatory subunit 8, also known as 26S proteasome AAA-ATPase subunit Rpt6, is an enzyme that in humans is encoded by the PSMC5 gene. This

26S protease regulatory subunit S10B, also known as 26S proteasome AAA-ATPase subunit Rpt4, is an enzyme that in humans is encoded by the PSMC6 gene. This

26S protease regulatory subunit 6B, also known as 26S proteasome AAA-ATPase subunit Rpt3, is an enzyme that in humans is encoded by the PSMC4 gene. This

ATPase, H+ transporting, lysosomal 38kDa, V0 subunit d2 is a protein in humans that is encoded by the ATP6V0D2 gene. It is part of proton pumps in the

mammalian mitochondrial DNA: coding portions of genes for 2 subunits of ATPase overlap. DNA encodes protein sequence by a series of three-nucleotide codons

this gene is a member of kinesin-like protein family, and contains common ATPase site structures such as the P-loop, Switch 1, and Switch 2. Most proteins

cascade, which activates H+-ATPase, a pump responsible for pumping H+ ions out of the cell. The phosphorylated H+-ATPase allows the binding of a 14-3-3

FO complex E subunit appears to play an important role in supporting F-ATPase dimerisation. This subunit is anchored to the inner mitochondrial membrane

at the N-terminal region exerts higher calcium sensitivity of actomyosin ATPase activity and myofilament force production, compared with the adult cardiac

26S protease regulatory subunit 4, also known as 26S proteasome AAA-ATPase subunit Rpt2, is an enzyme that in humans is encoded by the PSMC1 gene. This

accounts for less than 25% of cases, is caused by mutations in the Na+ /K+ -ATPase gene ATP1A2. FHM3 is a rare subtype of FHM and is caused by mutations in

that serves as a toxin due to its ability to inhibit calcium-dependent ATPases found in the endoplasmic and sarcoplasmic reticulum. This inhibition disrupts

in the human stomach lumen, a level maintained by the proton pump H+/K+ ATPase. The parietal cell releases bicarbonate into the bloodstream in the process

ejecting or restructuring nucleosomes. These protein complexes have a common ATPase domain and energy from the hydrolysis of ATP allows these remodeling complexes

TRPV5, TRPV6, TRPA1, mCa1, mCa2, CALHM1) TRPP3, a plant ion channel, Ca2+-ATPase, mitochondrial Ca2+ uniporter, tubulin, myosin light-chain phosphatase,

delta, mitochondrial, also known as ATP synthase F1 subunit delta or F-ATPase delta subunit is an enzyme that in humans is encoded by the ATP5F1D (formerly

encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane

stimulates the RNA polymerase II C-terminal domain kinase and DNA-dependent ATPase activities of TFIIH. Both TFIIH and TFIIE are required for promoter clearance

bloodstream. Potassium is not in fact lost from the body, but increased Na+/K+-ATPase activity (the enzyme that moves potassium into cells and keeps sodium in

26S proteasome non-ATPase regulatory subunit 2, also as known as 26S Proteasome Regulatory Subunit Rpn1 (systematic nomenclature), is an enzyme that in

member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have

26S proteasome non-ATPase regulatory subunit 5 is an enzyme that in humans is encoded by the PSMD5 gene. The 26S proteasome is a multicatalytic proteinase

26S proteasome non-ATPase regulatory subunit 8 is an enzyme that in humans is encoded by the PSMD8 gene. The 26S proteasome is a multicatalytic proteinase

26S proteasome non-ATPase regulatory subunit 10 or gankyrin is an enzyme that in humans is encoded by the PSMD10 gene. First isolated in 1998 by Tanaka

segment and introduction of 2 negative supercoils. N-gates are formed by ATPase domains of GyrB subunits. Binding of 2 ATP molecules leads to dimerization

26S proteasome non-ATPase regulatory subunit 14, also known as 26S proteasome non-ATPase subunit Rpn11, is an enzyme that in humans is encoded by the

encoded by the ATP11C gene. ATP11C encodes a member of the Type IV P-type ATPase family that is thought to transport or 'flip' aminophospholipids. The corresponding

26S proteasome non-ATPase regulatory subunit 4, also as known as 26S Proteasome Regulatory Subunit Rpn10 (systematic nomenclature), is an enzyme that in

s-like protein ATPase ASNA1: encoding enzyme ATPase ASNA1 also known as arsenical pump-driving ATPase and arsenite-stimulated ATPase BTBD14B: encoding

acid substitutions at well-defined positions of the α-subunit of Na+,K+-ATPase (ATPalpha). Variation in ATPalpha has been surveyed in various CTS-adapted

protein that in humans is encoded by the MYL1 gene. Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable

26S proteasome non-ATPase regulatory subunit 3 is an enzyme that in humans is encoded by the PSMD3 gene. The 26S proteasome is a multicatalytic proteinase

on among other things the content of myoglobin, mitochondria, and myosin ATPase etc.[citation needed] The word muscle comes from Latin musculus, diminutive

26S proteasome non-ATPase regulatory subunit 1, also as known as 26S Proteasome Regulatory Subunit Rpn2 (systematic nomenclature), is a protein that in

Homo sapiens ATPase, H+ transporting, lysosomal interacting protein 1 (ATP6IP1), ATP6V0A2 NM_012463 ATP6V0B NM_004047 Homo sapiens ATPase, H+ transporting

Acetylcholine transport utilizes a proton gradient established by a vacuolar ATPase. PET imaging of the VAChT may provide insights into early diagnosis of Alzheimer's

Homo sapiens ATPase, H+ transporting, lysosomal interacting protein 1 (ATP6IP1), ATP6V0A2 NM_012463 ATP6V0B NM_004047 Homo sapiens ATPase, H+ transporting

removed from the cell quickly enough. a. Plasma membrane Calcium ATPase (Ca ATPase) this primary active transporter pumps calcium out of the myocyte

26S proteasome non-ATPase regulatory subunit 12 is an enzyme that in humans is encoded by the PSMD12 gene. The 26S proteasome is a multicatalytic proteinase

pupylation. It is then recognized by the protein Mycobacterium proteasomal ATPase (Mpa), in a mechanism that induces folding of Pup. Mpa delivers the substrate

Activator of 90 kDa heat shock protein ATPase homolog 1 is an enzyme that in humans is encoded by the AHSA1 gene. AHSA1 has been shown to interact with

26S proteasome non-ATPase regulatory subunit 9 is an enzyme that in humans is encoded by the PSMD9 gene. The 26S proteasome is a multicatalytic proteinase

generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F1 - containing the extramembraneous

another protein embedded in their membrane: vacuolar-type H+-ATPase or V-ATPase. This ATPase pumps H+ ions into the vesicle lumen, lowering its pH with

thus leads to secretion. One example is gastrin, which stimulates the H/K ATPase in the parietal cells (increased gastric acid production by the stomach)

Sodium/potassium-transporting ATPase gamma chain is a protein that in humans is encoded by the FXYD2 gene. This gene encodes a member of a family of small

ATP-dependent processes, e.g. ATPases, such as acto-myosin ATPase and calcium ATPase involved in muscle contraction, and sodium/potassium ATPase involved in sodium

is a protein that in humans is encoded by the PEX6 gene. PEX6 is an AAA ATPase that localizes to the peroxisome. PEX6 forms a hexamer with PEX1 and is

26S proteasome non-ATPase regulatory subunit 11 is an enzyme that in humans is encoded by the PSMD11 gene. The 26S proteasome is a multicatalytic proteinase

subunit composition between mitochondrial, chloroplast and bacterial F-ATPases. In mitochondria, the peripheral stalk is composed of one copy each of

ATPase ASNA1 also known as arsenical pump-driving ATPase and arsenite-stimulated ATPase is an enzyme that in humans is encoded by the ASNA1 gene. ASNA1

26S proteasome non-ATPase regulatory subunit 13 is an enzyme that in humans is encoded by the PSMD13 gene. The 26S proteasome is a multicatalytic proteinase

Katanin p60 ATPase-containing subunit A1 is an enzyme that in humans is encoded by the KATNA1 gene. Microtubules, polymers of alpha and beta tubulin subunits

DNA-dependent ATPase, abbreviated Dda and also known as Dda helicase and Dda DNA helicase, is the 439-amino acid 49,897-atomic mass unit protein coded

dodecamer with RUVBL2 protein. Possesses single-stranded DNA-stimulated ATPase and ATP-dependent DNA helicase (3' to 5') activity; hexamerization is thought

Na+/K+-ATPase. However, in experiments with patients where the Na+/K+-ATPase had been blocked in the underarm by infusion of the Na+/K+-ATPase-blocker

Calponin is a calcium binding protein. Calponin tonically inhibits the ATPase activity of myosin in smooth muscle. Phosphorylation of calponin by a protein

page in the UCSC Genome Browser. Kinosita K, Yasuda R, Noji H (2003). "F1-ATPase: a highly efficient rotary ATP machine". Essays in Biochemistry. 35: 3–18

awarded to Danish chemist Jens Christian Skou for his discovery of the Na+/K+-ATPase. Boyer was born in Provo, Utah, and grew up in a nonpracticing Mormon family

It was here that Racker demonstrated that glycolysis was dependent on ATPase and the continuous regeneration of ADP and phosphate. Maynard E. Pullam

histamines in enterochromaffin-like cells, and it induces the insertion of K+/H+ ATPase pumps into the apical membrane of parietal cells (which in turn increases

luminal sodium channels. Aldosterone also increases the number of Na⁺/K⁺-ATPase pumps : 949  that allow increased sodium reabsorption and potassium excretion

possess an F-type ATPase (unusual for archaea, but common for bacteria, mitochondria and chloroplasts) along with an A-type ATPase. The fusaro strain

The ATPase assay is a membrane assay that indirectly measures the activity of efflux transporters. ATP Binding Cassette or efflux transporters mediate

research focuses on two proteins: the Ca2+-ATPase of muscle sarcoplasmic reticulum, and the Na+, K+-ATPase expressed in all animal cells. He is a professor

subunit of the bacterial Sec export pathway and of a protein-secreting ATPase complex, also known as a SecYEG translocon. Homologs of the SecYEG complex

kinase, and Na+/K+-ATPase (synaptosomal membrane). Melittin blocks transport pumps such as the Na+-K+-ATPase and the H+-K+-ATPase. Melittin is the main

a result of sodium transport from the lumen into the blood by the Na+/K+ATPase in the basolateral membrane of the epithelial cells. Thus, the glomerular

water in the presence of extracellular sodium and is driven by the NA+/K+-ATPase pump. In the roots of plants, the H+/K+ symporters are only one member of

26S proteasome non-ATPase regulatory subunit 6 is an enzyme that in humans is encoded by the PSMD6 gene. The proteasome and its subunits are of clinical

pregnancy and breastfeeding is of unclear safety. It works by blocking H+/K+-ATPase in the parietal cells of the stomach. Dexlansoprazole was approved for medical

Hsp70 and Hsp90. They are particularly essential in stimulation of the ATPase activity of these chaperone proteins. There are a great number of different

possess an F-type ATPase (unusual for archaea, but common for bacteria, mitochondria and chloroplasts) along with an A-type ATPase. M. acetivorans has

The term was introduced by Chetverin to make nomenclature in the Na/K-ATPase enzyme unambiguous. This enzyme is composed of two subunits: a large, catalytic

Failure to do so is one cause of muscle cramps. The plasma membrane Ca2+ ATPase and the sodium-calcium exchanger are together the main regulators of cytoplasmic

they are neither cytotoxic nor fluorescent. Blebbistatin inhibits myosin ATPase activity and this way acto-myosin based motility. It binds halfway between

Ouabain and digitoxin. It specifically inhibits the membrane protein Na+/ K+ ATPase in muscle tissue (heart) which can lead to Ca2+ overload, diastolic dysfunction

and transcription. The ALC1 comprises ATPase domain and macro domain. On the basis of homology within the ATPase domain, ALC1 belongs to Snf2 family. It

the Na,K-ATPase. Each of these auxiliary subunits produces a distinct functional effect on the transport characteristics of the Na,K-ATPase that is adjusted

pregnancy and breastfeeding is of unclear safety. It works by blocking H+/K+-ATPase in the parietal cells of the stomach. Lansoprazole was patented in 1984

together with TPR (ERCC6L)domain and Stimulates the ERCC6L translocase and ATPase activities. Rampalli S, Pavithra L, Bhatt A, Kundu TK, Chattopadhyay S (October

environment of the early endosome, generated by a vacuolar membrane proton pump V-ATPase. On the other hand, epidermal growth factor (EGF) and the EGF receptor have

endosomes of PTCs where it co-localizes with the electrogenic vacuolar H+‐ATPase (V‐ATPase). ClC-5 in this compartment contributes to the maintenance of intra-endosomal

ATPase WRNIP1 is an enzyme that is encoded by the WRNIP1 gene in humans. The protein is a member of AAA ATPase family. Werner's syndrome is a rare autosomal

required for normal levels of sodium-calcium exchanger, sodium potassium ATPase and inositol triphosphate receptor in cardiomyocytes, and is regulated by

that is needed for the secretion of gastric acid. It is a specific H+/K+ATPase inhibitor. This is the enzyme needed for the final step in the secretion

that in humans is encoded by the SLN gene. Sarcoplasmic reticulum Ca2+-ATPases are transmembrane proteins that catalyze the ATP-dependent transport of

presence. Low(er) myosin ATPase, sensitive to alkali. IIa (Fast oxidative/glycolytic, FOG) — High glycolytic, oxidative and myosin ATPase presence, sensitive

Mi-2/NuRD was the only known protein complex that couples chromatin remodeling ATPase and chromatin deacetylation enzymatic functions. In 1998, several independent

amongst all members of the order, albeit only at the amino-acid level, is the ATPase subunit of the DNA terminase; the latter is involved in the packaging of

that decreases gastric acid secretion. It works by inactivating (H+/K+)-ATPase function in the stomach. Study of pantoprazole began in 1985, and it came

In molecular biology, ATP10 protein (mitochondrial ATPase complex subunit ATP10) is an ATP synthase assembly factor. It is essential for the assembly of

[citation needed] An example of active transport of ions is the Na+-K+-ATPase (NKA). NKA is powered by the hydrolysis of ATP into ADP and an inorganic

potassium channels, and/or the electrogenic response of the sodium-potassium ATPase. Depending on neuron type and stimulus used for induction, slow afterhyperpolarisations

Obg-like ATPase 1 is an enzyme that in humans is encoded by the OLA1 gene. Ola1 belongs to the protein family of Obg-like GTPases but defines an exceptional

Kotenyova T, Moche M, Schüler H (11 January 2010). "Crystal structures of the ATPase domains of four human Hsp70 isoforms: HSPA1L/Hsp70-hom, HSPA2/Hsp70-2, HSPA6/Hsp70B'

(also known as F1Fo ATPase, or H(+)-transporting two-sector ATPase) (EC 3.6.3.14) are composed of two linked complexes: the F1 ATPase complex is the catalytic

regulation TOR (target of rapamycin) Others API5 (Apoptosis inhibitor 5) V-type ATPase H subunit Cho, Uhn Soo; Xu, Wenqing (1 November 2006). "Crystal structure

protein that in humans is encoded by the MDN1 gene. Midasin is a member AAA ATPase family. ENSG00000288121 GRCh38: Ensembl release 89: ENSG00000112159, ENSG00000288121

Calcium-ATPases decreases intracellular calcium concentration by pumping calcium ions to the outside of the cell (this allows for the H+-ATPase to be reactivated

regulation TOR (target of rapamycin) Others API5 (Apoptosis inhibitor 5) V-type ATPase H subunit Cho, Uhn Soo; Xu, Wenqing (1 November 2006). "Crystal structure

currently unknown. There is no counterpart in chloroplast or bacterial F-ATPases identified so far. GRCh38: Ensembl release 89: ENSG00000167283 – Ensembl

N-terminal globular head that harbors the catalytically active, magnesium(Mg)-ATPase. The C-terminal rod domain is an alpha helical coiled-coil that can multimerize

phosphorylation. F-type ATPases (Adenylpyrophosphatase ) typically use protons as the sole coupling ion, but the F1F0 ATPase of Propionigenium modestum

the Na+/K+-ATPase function. The Na+/K+-ATPase activity has been shown to be significantly reduced during estivation. As the Na+/K+-ATPase pump uses quite

Another example of the importance of reaction intermediates is seen with AAA-ATPase p97, a protein that used in a variety of cellular metabolic processes. p97

function ATPase-coupled transmembrane transporter activity nucleotide binding ATPase activity hydrolase activity ATP binding transporter activity ATPase-coupled

(common, via Na+/K+-ATPase, increased by aldosterone), or reabsorption (rare, hydrogen potassium ATPase) Calcium Uses calcium ATPase, sodium-calcium exchanger

transmembrane transporter activity ATPase activity ATP binding ATPase-coupled inorganic anion transmembrane transporter activity ATPase-coupled transmembrane transporter

organelles during interphase. Katanin is a heterodimer that consists of a 60 kDa ATPase (p60 subunit A 1) and an 80 kDa accessory protein (p80 subunit B 1). The

luminal domain of LAP1 interacts with Torsin A and is necessary for the ATPase activity of Torsin A. LAP1 plays a critical role in skeletal and heart muscle

the ENTPD5 gene. ENTPD5 is similar to E-type nucleotidases (NTPases)/ecto-ATPase/apyrases. NTPases, such as CD39, mediate catabolism of extracellular nucleotides

and a central AAA-ATPase domain. The MIT domain is responsible for the interaction of Vps4 with the MIM domain of Vps2. The AAA-ATPase domain hydrolyzes

derived from striated muscle to study the kinetic mechanism of the actomyosin ATPase cycle. The main focus was to determine how the hydrolysis of ATP by enzymes

In marine teleost fish, by expending energy to power the enzyme Na+/K+-ATPase and in coordination with other protein transporters, ionocytes pump excessive

transferase activity nucleotide binding protein kinase activity ATPase binding ATPase regulator activity metal ion binding kinase activity protein kinase

Molecular function ATPase binding misfolded protein binding Hsp70 protein binding protein binding oxidoreductase activity chaperone binding ATPase activator activity

ATPase Domain 3B (ATAD3B) is a protein that in humans is encoded by the ATAD3B gene. [citation needed] ATAD3 is part of the AAA protein family. The function

"Characterization of the macrocyclic carbon suboxide factors as potent Na,K-ATPase and SR Ca-ATPase inhibitors". Biochimica et Biophysica Acta (BBA) - Biomembranes

function nucleotide binding ATPase activity ATP binding ATPase-coupled inorganic anion transmembrane transporter activity ATPase-coupled transmembrane transporter

between mitochondrial, chloroplast and bacterial F-ATPases. In bacterial and chloroplast F-ATPases, the peripheral stalk is composed of one copy of the

Molecular function nucleotide binding ATPase activity ATP binding 15-hydroxyprostaglandin dehydrogenase (NAD+) activity ATPase-coupled inorganic anion transmembrane

function nucleotide binding microtubule motor activity tubulin-dependent ATPase activity microtubule binding microtubule plus-end binding protein binding

ontology Molecular function ATPase-coupled transmembrane transporter activity nucleotide binding ATPase activity ATP binding ATPase-coupled inorganic anion

convoluted tubule possess the ATP-powered sodium-potassium antiporter (Na+/K+-ATPase), which uses energy from ATP to transfer three sodium ions out from the

exon junction core complex is locked onto RNA by inhibition of eIF4AIII ATPase activity". Nat. Struct. Mol. Biol. 12 (10): 861–9. doi:10.1038/nsmb990.

characterization has been performed for ArlI, a Type II/IV secretion system ATPase super-family member and PibD/ArlK. ArlI forms a hexamer which hydrolyses

AHSA2 also known as AHA1, activator of heat shock 90kDa protein ATPase homolog 2 (yeast) is a human gene which encodes a protein which acts as co-chaperone

Molecular function ATPase-coupled transmembrane transporter activity nucleotide binding organic anion transmembrane transporter activity ATPase activity ATP

less specifically the S-isomer) of omeprazole. It works by blocking H+/K+-ATPase in the parietal cells of the stomach. It was patented in 1993 and approved

TEA, but also its ability to inhibit Na,K-ATPase. Acting on the extracellular vestibule of the Na,K-ATPase, inhibiting K+ access similar to ouabain, TEA

protein, ATOX1 is responsible for shuttling copper from the cytosol to ATPase transporters ATP7A and ATP7B that move copper to the trans-Golgi network

receptor activity ATPase activity ATP binding ATPase-coupled inorganic anion transmembrane transporter activity potassium channel activity ATPase-coupled transmembrane

where the hydrolysis of ATP to ADP and an inorganic phosphate at the P-type ATPase moves 3 potassium ions back out of the cell and 2 sodium ions into the cell

K+-ATPase in congestive heart failure or arrythmias, which causes an inotropic effect, same as many other digitalis like compounds. The Na+,K+-ATPase creates

composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed

Gene ontology Molecular function nucleotide binding ATPase activity ATP binding ATPase-coupled transmembrane transporter activity lipid transporter activity

exon junction core complex is locked onto RNA by inhibition of eIF4AIII ATPase activity". Nat. Struct. Mol. Biol. 12 (10): 861–9. doi:10.1038/nsmb990.

Hydrogen ATPase commonly refers to: Hydrogen potassium ATPase, the gastric proton pump. V-ATPase, the synaptic vesicle transporter. This set index page

inhibits adenosine 5’-triphosphate (ATP)-hydrolytic action of myocardial Na+K+ATPase in-vitro in a concentration dependent manner. The mode of action and the

characterization has been performed for ArlI, a Type II/IV secretion system ATPase super-family member and PibD/ArlK. ArlI forms a hexamer which hydrolyses

Proteasomal ATPase-associated factor 1 is an enzyme that in humans is encoded by the PAAF1 gene. PAAF1 has been shown to interact with PSMD10. GRCh38:

The inhibition of Na+/K+ -ATPase is due to increased compression due to pressure. The rate-limiting step of the Na+/K+ -ATPase reaction induces an expansion

by the Na+/K+-ATPase in the basolateral membrane of the epithelial cells. Sodium reabsorption is primarily driven by this P-type ATPase – 60–70% of the

proteins encoded by the minB operon and also a part of the ParA family of ATPases. It is required to generate pole to pole oscillations prior to bacterial

synthase delta/epsilon subunit is a part of the ATP synthase and the F-ATPase family in general. It is known as the delta subunit in mitochondrial ATP

Fo complex subunit s (factor B) Kinosita K, Yasuda R, Noji H (2003). "F1-ATPase: a highly efficient rotary ATP machine". Essays Biochem. 35: 3–18. doi:10

page in the UCSC Genome Browser. Kinosita K, Yasuda R, Noji H (2003). "F1-ATPase: a highly efficient rotary ATP machine". Essays Biochem. 35: 3–18. doi:10

composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed

family of ecto-nucleosidases that hydrolyze 5'-triphosphates. This ecto-ATPase is an integral membrane protein. Alternative splicing of this gene results

with the 36 and 40 kDa subunits. The core complex possesses DNA-dependent ATPase activity, which was found to be stimulated by PCNA in an in vitro system

repair of DNA. This protein binds to double-stranded DNA, and displays ATPase activity in the presence of DNA. This gene is highly expressed in testis

ontology Molecular function ATPase-coupled transmembrane transporter activity apolipoprotein binding nucleotide binding ATPase binding apolipoprotein A-I

Tatishchev S, Kurtz I (March 2003). "The COOH termini of NBC3 and the 56-kDa H+-ATPase subunit are PDZ motifs involved in their interaction". Am. J. Physiol.,

budding yeast, the analog for TRIP13 is PCH2. TRIP13 is a member of the AAA+ ATPase family, a family known for mechanical forces derived from ATP hydrolase

composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed

"Human liver cDNA clones encoding proteolipid subunit 9 of the mitochondrial ATPase complex". Biochem. Biophys. Res. Commun. 144 (3): 1257–64. doi:10

RNF213 is a 591kDa cytosolic E3 ubiquitin ligase with RING finger and AAA+ ATPase domains. Chromosome-wide linkage analysis found that moyamoya disease locus

subunit of the F1Fo ATPase, also known as Complex V, which consists of 14 nuclear- and 2 mitochondrial-encoded subunits. F-type ATPases consist of two structural

triphosphatase (H+/K+ ATPase) acid pump. The term "proton pump inhibitor" comes from the recognition of hydrogen cations as a single proton. H+/K+ ATPase pumps, found

is involved in Notch signalling by regulating the vacuolar proton pump V-ATPase. DmX is a highly conserved gene and is widely found in insects and mammals

apolipoprotein A-I receptor binding ATPase activity protein binding signaling receptor binding ATP binding ATPase-coupled lipid transmembrane transporter

responsible for muscle contraction, transport in the cell, energy generation (F1-ATPase), DNA replication and transcription (polymerases), DNA unknotting and unwinding

hereditary causes include mutations of subunits of the apical proton pump vH+-ATPase, which are transmitted in an autosomal recessive fashion, and may be associated

AFG3 ATPase family gene 3-like 2 (S. cerevisiae) is a protein that in humans is encoded by the AFG3L2 gene. This gene encodes a protein localized in mitochondria

protein binding ATPase activity protein binding MHC class I protein binding TAP1 binding ATP binding peptide antigen binding ADP binding ATPase-coupled transmembrane

pregnancy and breastfeeding is of unclear safety. It works by blocking H+/K+-ATPase in the parietal cells of the stomach. Rabeprazole was patented in 1986,

composed of a base, which contains 6 ATPase subunits and 2 non-ATPase subunits, and a lid, which contains up to 10 non-ATPase subunits. Proteasomes are distributed

radiation striking a surface which is reflected off it.), and increased Na+/K+-ATPase in the gills. A number of mechanisms assist with osmoregulation. Nichols

according to simulation, would facilitate its binding with the Na+/K+-ATPase. Some of the organisms that contain palytoxin or its close analogues are

to the endoplasmic reticulum and contiguous perinuclear space, where its ATPase activity is activated by either LULL1 or LAP1, respectively. The protein

5×10−3 0.10 0.037 Yes (e.g. Na+/K+-ATPase) Hypernatremia 1 17 Chlorine 1.5×10−3 0.095 0.024 Yes (e.g. Cl-transporting ATPase) Hyperchloremia 17 12 Magnesium

nucleotide binding ATPase activity protein binding ATP binding cholesterol transfer activity protein heterodimerization activity ATPase-coupled transmembrane

hypothermia, ATPase activity is markedly reduced at 10 °C. There are, however, tissue and species differences in the cold sensitivity of this ATPase which may

with the 38 and 40 kDa subunits. The core complex possesses DNA-dependent ATPase activity, which was found to be stimulated by PCNA in an in vitro system

sometimes associated with the outer mitochondrial membrane, has a weak ATPase activity and contains 6 TPR repeats. GRCh38: Ensembl release 89: ENSG00000025772

TREK). Temperature also modulates the activity of the Na+/K+-ATPase. The Na+/K+-ATPase is a P-type pump that extrudes 3Na+ ions in exchange for 2K+ ions

Folliculin-interacting protein 1 (FNIP1) functions as a co-chaperone which inhibits the ATPase activity of the chaperone Hsp90 (heat shock protein-90) and decelerates

domain is a protein domain found in AAA ATPases including cell division protein 48 (CDC48), VCP-like ATPase and N-ethylmaleimide sensitive fusion protein

DNA polymerase accessory protein. Replication factor C is a DNA-dependent ATPase that is required for eukaryotic DNA replication and repair. The protein

protein. The actions of the Na-K-ATPase enzyme relate with the creation of calcium-signaling microdomains. Na-K-ATPase is a protein that pumps Na+ and

PXK gene. PXK binds to the Na⁺/K⁺-ATPase beta-1 (ATP1B1) and beta-3 (ATP1B3) subunits and modulates both Na⁺/K⁺-ATPase enzymatic and ion pump activities

The protein encoded by this gene is a member of the AAA protein family (ATPases associated with diverse cellular activities), and is the homolog of the

the cell membrane. Osmolyte Myo-Inositol Taurine and Taurine-transporting ATPase Creatine Betaines Trimethylglycine – A Betaine and metabolite of Choline

function nucleotide binding heme transmembrane transporter activity ATPase activity ATPase-coupled transmembrane transporter activity ATP binding Cellular

twitch muscles. Although slower, the sarco/endoplasmic reticulum calcium-ATPase (SERCA) actively pumps Ca2+ back into the sarcoplasmic reticulum, resulting

Perrault syndrome and cause a variety of molecular defects, from the loss of ATPase docking, to the activation or inhibition of peptidase activity. Endopeptidase

TREK). Temperature also modulates the activity of the Na+/K+-ATPase. The Na+/K+-ATPase is a P-type pump that extrudes 3Na+ ions in exchange for 2K+ ions

CLPX gene. This protein is a member of the family of AAA Proteins (AAA+ ATPase) and is to form the protein complex of Clp protease (Endopeptidase Clp)

S, Wiederhold T, Marshansky V, et al. (2000). "The B1 subunit of the H+ATPase is a PDZ domain-binding protein. Colocalization with NHE-RF in renal B-intercalated

primarily on the type of NTPases: Type I : Walker type P-loop ATPase Type II : Actin-like ATPase Type III : tubulin-like GTPase Type IV : No NTPase This system

tubule of a nephron and stimulation of aldosterone that activates Na+/K+-ATPase at collecting duct. Inhibition of sodium-chloride symporter increases availability

Water uptake. This follows the osmotic gradient established by Na+/K+ ATPase on the basolateral surface. This can occur transcellularly or paracellularly

interactions. The encoded protein has been shown to have dsDNA-dependent ATPase activity and RNA polymerase II termination activity. This protein interacts

FtsH-homology protease domain as well as an AAA+ homology ATPase domain. The protein is thought to use ATPase-driven conformational changes to the AAA-domain in

aldosterone increases activity of basolateral membrane sodium-potassium ATPase and apical epithelial sodium channels, ENaC, as well as potassium channels

1hjo: HEAT-SHOCK 70KD PROTEIN 42KD ATPASE N-TERMINAL DOMAIN 1s3x: The crystal structure of the human Hsp70 ATPase domain 1xqs: Crystal structure of the

animal model of hypertension. It modulates the effects of the enzyme Na+/K+-ATPase, which maintains sodium and potassium ion gradients across plasma membranes

noting "an ATPase most similar to the mimivirus homologue" and a major capsid protein phylogeny that is "not compatible with that of the ATPase phylogeny"

subunit of Escherichia coli F1-ATPase enzyme. In her graduate work, Rao discovered that three catalytic sites in the ATPase enzyme needed to interact to

(RFC) and identification of an RFC subcomplex possessing DNA-dependent ATPase activity". The Journal of Biological Chemistry. 273 (10): 5979–87. doi:10

(Related to Ion Channel). FXYD2, also known as the gamma subunit of the Na,K-ATPase, regulates the properties of that enzyme. FXYD1 (phospholemman), FXYD2 (gamma)

F-type may refer to: F-type asteroid, a type of carbonaceous asteroid F-ATPase, a membrane protein F-type main-sequence star, a hydrogen-fusing star F-type

Kisilevsky et al., 2008). Direct interaction of D1 and D2 receptors and Na+-K+-ATPase has also been demonstrated (Hazelwood et al., 2008; Blom et al., 2012).

includes the expression of the calcium ATPase, regulation of ion channels, oxidative phosphorylation, increased Na-K-ATPase activity, increased carbohydrate

synchronizes an array of biological processes, (such as Ca2+, Na+, K+ -ATPase) thus maintaining membrane potential and controlling intracellular pH and

creatures, V-ATPase is a necessary component for life but Nelson discovered that yeast can overcome the constraints of non-function V-ATPase when living

Sodium/potassium transporting ATPase interacting 1 is a protein that in humans is encoded by the NKAIN1 gene. NKAIN1 is a member of a family of mammalian

well as contractive responses of smooth muscles and inhibition of Na/K-ATPase (NaKATPase). Furthermore, in vitro activity against Mycobacterium tuberculosis

are secreted via both H+-K+ATPases and H+ ATP-ases on the apical/luminal surface of the cell. By definition, the H+-K+ATPase reabsorbs one potassium ion

by a "pushing" ATPase known as SecA, sometimes assisted by the SecDF complex on the other side responsible for pulling. The SecA ATPase uses a "push-and-slide"

calmodulin binding protein. Like calponin, caldesmon tonically inhibits the ATPase activity of myosin in smooth muscle. This gene encodes a calmodulin- and

later stages of life. Tight regulation of Na/K-ATPase and an overall decrease in expression of H-ATPase assists in regulating the lamprey's internal fluid

calmodulin binding protein. Like calponin, caldesmon tonically inhibits the ATPase activity of myosin in smooth muscle. This gene encodes a calmodulin- and

later stages of life. Tight regulation of Na/K-ATPase and an overall decrease in expression of H-ATPase assists in regulating the lamprey's internal fluid

gastric parietal cell M3 receptors, causing insertion of hydrogen potassium ATPase vesicles into the apical plasma membrane. The end result is increased secretion

D; Jacinto, António; Certal, Ana C; Rodríguez-León, Joaquín (2014). "V-ATPase Proton Pumping Activity is Required for Adult Zebrafish Appendage Regeneration"

Gene ontology Molecular function ATPase activity protein binding ATP binding ATPase-coupled transmembrane transporter activity metal ion binding cholesterol

membrane. MinD localizes to the membrane only at cell poles and contains an ATPase and an ATP-binding domain. MinD is only able to bind to the membrane when

cyclobutyl dimer formation. Two UvrA proteins form a dimer and they both have ATPase/GTPase activity. The UvrA dimer binds with a UvrB dimer and forms a complex

PfATPase6, is a calcium ATPase gene encoded by the malaria parasite Plasmodium falciparum. The protein is thought to be a P-type ATPase involved in calcium

well as contractive responses of smooth muscles and inhibition of Na/K-ATPase (NaKATPase). Furthermore, in vitro activity against Mycobacterium tuberculosis

binding phosphatidylinositol-3,4,5-trisphosphate binding lipid binding ATPase activity Cellular component cytoplasm endosome early endosome membrane membrane

protein homodimerization activity transporter activity ATPase activity protein binding ATP binding ATPase-coupled transmembrane transporter activity cholesterol

mTOR complex 1. The LAMTOR subunits form a complex with Rag GTPase and v-ATPase, which sits on the cell’s lysosomes and detects the availability of amino

Molecular function nucleotide binding ATPase activity ATP binding ABC-type xenobiotic transporter activity ATPase-coupled transmembrane transporter activity

Sigala B, Saibil H, Tsaneva IR (Feb 2007). "Dodecameric structure and ATPase activity of the human TIP48/TIP49 complex". Journal of Molecular Biology

is dependent on concentrations of Ca2+ in the cytosol, either via Ca,Mg-ATPase from the sarcoplasmic reticulum or voltage-gated calcium channels from the

simultaneously for reduction to occur. ArsA and ArsB form an anion-translocating ATPase. The ArsB protein is distinguished by its overall hydrophobic character

2008). "A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes". EMBO Rep. 9 (7): 648–54

the mitochondrial genome. His landmark crystallographic studies of the F1-ATPase, the catalytic region of the ATP synthase (done in collaboration with crystallographer

Alternative oxidase Cytochrome bc1 complex Cytochrome c Cytochrome c oxidase F-ATPase ATP–ADP translocase ATP-binding cassette transporter Cholesterol side-chain

Sanguinarine is a toxin that kills animal cells through its action on the Na+/K+-ATPase transmembrane protein. Epidemic dropsy is a disease that results from ingesting

gene ATP1A3, among other genes that are not ion transporters. Template: ATPase disorders (ion pumps) Kim JB (January 2014). "Channelopathies". Korean Journal

Vacuolar ATPase (vATPase) maintains the acidic pH in lysosomes and it has been shown that TMEM106B interacts with accessory proteins of vATPase. When TMEM106B

SH (August 2001). "Atp11p and Atp12p are assembly factors for the F(1)-ATPase in human mitochondria". J. Biol. Chem. 276 (33): 30773–8. doi:10.1074/jbc

reason for the high sensitivity of fish is the effect of bifenthrin as ATPase-inhibitor. The gills need ATP to control the osmotic balance of oxygen.

Gene ontology Molecular function ATPase-coupled transmembrane transporter activity nucleotide binding ATPase activity ATP binding transporter activity

crystallography) by John Kendrew and colleagues in England. The discovery of Na+/K+-ATPase, the first antiporter enzyme identified, is published by Jens Christian

Program [1] Garg LC, Narang N (1989). "Suppression of ouabain-insensitive K-ATPase activity in rabbit nephron segments during chronic hyperkalemia". Renal

Gene ontology Molecular function nucleotide binding microtubule binding ATPase activity ATP binding microtubule motor activity minus-end-directed microtubule

function microtubule motor activity nucleotide binding microtubule binding ATPase activity protein binding ATP binding Cellular component cytoplasm endosome

member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes

actin attachment time as that of β. It is the enzymatic activity of the ATPase in the myosin head that cyclically hydrolyzes ATP, fueling the myosin power

"Human liver cDNA clones encoding proteolipid subunit 9 of the mitochondrial ATPase complex". Biochemical and Biophysical Research Communications. 144 (3):

inhibition of sodium/potassium adenosine triphosphatase (Na+/K+ ATPase). Na+/K+ ATPase inhibition increases intracellular sodium levels, which reverses

to produce VP2 and VP4. Other cleavage products include 3B (VPg), 2C (an ATPase), and 3D (the RNA polymerase). Genomic RNAs of picornaviruses possess multiple

with certain mutant proteins or complexes. Mutations in genes affecting V-ATPase synthesis and assembly, vesicle transport machinery, and protein sorting

family. The encoded protein is required for the activity of a vacuolar ATPase, which is responsible for proton pumping occurring in the acidification

superfamily are unified by the presence of the eponymous type IV pilin, an AAA+ ATPase, an integral (cytoplasmic) membrane (IM) platform, and (with the exception

to produce VP2 and VP4. Other cleavage products include 3B (VPg), 2C (an ATPase), and 3D (the RNA polymerase). Genomic RNAs of picornaviruses possess multiple

AMPK-activating effects. PEN2-metformin in turn binds to ATP6AP1 to inhibit v-ATPase activity. GRCh38: Ensembl release 89: ENSG00000205155 – Ensembl, May 2017

binding microtubule binding minus-end-directed microtubule motor activity ATPase activity protein binding ATP binding Cellular component cytoplasm centrosome

The net influx of Na+ ions and the compensatory activation of Na+ /K+ -ATPase to maintain ionic equilibrium within the RBC results in a steady decline

function microtubule binding microtubule motor activity nucleotide binding ATPase activity ATP binding minus-end-directed microtubule motor activity Cellular

plus-end-directed microtubule motor activity microtubule motor activity ATPase activity Cellular component nuclear matrix cytoplasm cytosol microtubule

Gene ontology Molecular function ATPase-coupled transmembrane transporter activity nucleotide binding ATPase activity protein binding ATP binding protein

ontology Molecular function microtubule motor activity nucleotide binding ATPase activity cytoskeletal motor activity ATP binding minus-end-directed microtubule

function microtubule binding microtubule motor activity nucleotide binding ATPase activity protein binding ATP binding identical protein binding Cellular

Molecular function unfolded protein binding ATPase binding Hsp70 protein binding chaperone binding protein binding ATPase activator activity transcription corepressor

function microtubule binding microtubule motor activity nucleotide binding ATPase activity ATP binding molecular function Cellular component cytoplasm microtubule

(May 2003). "The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes". Nature Cell Biology. 5 (5): 454–60. doi:10.1038/ncb982

microtubule motor activity plus-end-directed microtubule motor activity ATPase activity Cellular component cytoplasm cell projection cilium microtubule

Gene ontology Molecular function ATPase activity nucleotide binding ATP binding ATPase-coupled transmembrane transporter activity Cellular component membrane

tropomyosin, and troponin I which has an inhibitory action annulating the S1 ATPase activity in the presence of tropomyosin and troponin and absence of Ca2+)

Arenobufagin inhibits the sodium-potassium adenosine triphosphatase (Na+/K+-ATPase) . It is one of the most potent blockers that are known to science, along

function microtubule binding microtubule motor activity nucleotide binding ATPase activity plus-end-directed microtubule motor activity ATP binding Cellular

shared a haplotype with each other using several mitochondrial gene markers (ATPase 6, ND2, and ND5), while the octopuses in the southern provinces shared different

share the existence of an ATPase motor which facilitates chromatin sliding on DNA through the binding and hydrolysis of ATP. ATPase has an open and closed

7554/eLife.41444. PMC 6447362. PMID 30907728. "UPF1 UPF1 RNA helicase and ATPase [ Homo sapiens (human) ]". Lykke-Andersen J (2002). "Identification of a

focusing in immobilized pH gradients. Its effects on dog kidney Na+/K+-ATPase and rat brain GABA receptors have also been studied. ADA does, however,

The protein encoded by this gene is a member of the AAA protein family (ATPases associated with diverse cellular activities), and is the homolog of the

transmembrane transporter activity ATPase activity ATP binding purine nucleotide transmembrane transporter activity ATPase-coupled inorganic anion transmembrane

Gene ontology Molecular function nucleotide binding ATPase activity protein homodimerization activity transmembrane transporter activity ABC-type oligopeptide

structural characteristics: an ATP-binding cassette-like 'head' domain with ATPase activity (formed by the interaction of the N- and C- terminals) and a hinge

metal binding. The fourth HMA domain of the Menke's copper transporting ATPase shows a well-defined structure comprising a four-stranded antiparallel beta-sheet

subunit of 19S proteasome complex. The gene ADRM1 encodes one of the non-ATPase subunits of the 19S regulator base, subunit Rpn13. The human PSMD4 gene

Ballar Petek; Apostolou Andria; Agami Reuven; Fang Shengyun (Oct 2004). "AAA ATPase p97/valosin-containing protein interacts with gp78, a ubiquitin ligase for

function ATPase-coupled transmembrane transporter activity nucleotide binding protein homodimerization activity transporter activity ATPase activity protein

of the MJ1267 ATP binding cassette reveal an induced-fit effect at the ATPase active site of an ABC transporter". Structure. 9 (7): 571–86. doi:10

Gene ontology Molecular function ATPase-coupled transmembrane transporter activity nucleotide binding heme transmembrane transporter activity ABC-type

modulating: 1) chaperone-substrate affinity and specificity 2) chaperone ATPase and therefore its refolding activity 3) chaperone localization 4) chaperone-co-chaperone

microtubule motor activity microtubule binding ATP binding protein binding ATPase activity Cellular component spindle cytoplasm kinesin complex nucleus membrane

proteins (Trk) and V-type sodium ATP synthase subunit J or translocating ATPase J (EC). These proteins are involved in active sodium uptake utilizing ATP