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Information on EC 7.3.2.3 - ABC-type sulfate transporter
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7.3.2.3 ABC-type sulfate transporterIUBMB Comments
An ATP-binding cassette (ABC) type transporter, characterized by the presence of two similar ATP-binding domains/proteins and two integral membrane domains/proteins. The enzyme from Escherichia coli can interact with either of two periplasmic binding proteins and mediates the high affinity uptake of sulfate and thiosulfate. May also be involved in the uptake of selenite, selenate and possibly molybdate. Does not undergo phosphorylation during the transport.
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Word Map
- 7.3.2.3
- chromatin
- sulfur
- vacuolar
- proteasome
- dysplasia
-
diastrophic
- nucleosome
-
chromatin-remodeling
- mtdnas
-
chondrodysplasias
-
epiphyseal
-
brahma-related
-
sulfurylase
- malk
- v-atpase
-
brahma
-
v-type
- selenate
-
anti-sigma
- clpx
- osteochondrodysplasias
-
undersulfation
-
male-sterile
- rpt6
-
smarca4
-
apocytochrome
-
terminase
-
na+-independent
The expected taxonomic range for this enzyme is: Bacteria, Eukaryota
Reaction Schemes
+
+
=
+
+
+
+
+
sulfate-[sulfate-binding protein][side 1]
=
+
+
+
[sulfate-binding protein][side 1]
Synonyms
atpase subunit, sulfate transporter, rv1739c, 
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SYNONYM 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
EC 3.6.3.25
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-
formerly
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Rv1739c
sulfate transporter
sulfate-transporting ATPase
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-
-
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REACTION
REACTION DIAGRAM
COMMENTARY
ORGANISM
UNIPROT
LITERATURE
ATP + H2O + sulfate-[sulfate-binding protein][side 1] = ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1]
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-
-
-
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REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
hydrolysis of phosphoric ester
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-
-
-
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PATHWAY SOURCE
PATHWAYS
KEGG
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SYSTEMATIC NAME
IUBMB Comments
ATP phosphohydrolase (ABC-type, sulfate-importing)
An ATP-binding cassette (ABC) type transporter, characterized by the presence of two similar ATP-binding domains/proteins and two integral membrane domains/proteins. The enzyme from Escherichia coli can interact with either of two periplasmic binding proteins and mediates the high affinity uptake of sulfate and thiosulfate. May also be involved in the uptake of selenite, selenate and possibly molybdate. Does not undergo phosphorylation during the transport.
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SUBSTRATE
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
ATP + H2O + sulfate-[sulfate-binding protein][side 1]
ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1] + H+
ATP + H2O + sulfate-[sulfate-binding protein][side 1]
ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1] + H+
-
-
-
-
?
ATP + H2O + sulfate-[sulfate-binding protein][side 1]
ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1] + H+
-
-
-
-
?
ATP + H2O + sulfate/out
ADP + phosphate + sulfate/in
-
-
-
-
?
ATP + H2O + sulfate/out
ADP + phosphate + sulfate/in
-
transport of sulfate and thiosulfate
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?
ATP + H2O + sulfate/out
ADP + phosphate + sulfate/in
-
facilitation of bacterial sulfate uptake by Rv1739c requires CysA and its associated sulfate permease activity, thus Rv1739c may be a CysTWA-dependent sulfate transporter
-
-
?
ATP + H2O + sulfate/out
ADP + phosphate + sulfate/in
-
facilitation of bacterial sulfate uptake by Rv1739c requires CysA and its associated sulfate permease activity, thus Rv1739c may be a CysTWA-dependent sulfate transporter
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-
?
ATP + H2O + thiosulfate/out
ADP + phosphate + thiosulfate/in
-
-
-
-
?
ATP + H2O + thiosulfate/out
ADP + phosphate + thiosulfate/in
-
transport of sulfate and thiosulfate
-
?
ATP + H2O + thiosulfate/out
ADP + phosphate + thiosulfate/in
-
thiosulfate can be transported by two permease systems. One of theses systems is the sulfate permease, while the other does not required cysT and cysW gene products but uses other integral membrane components
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-
?
additional information
?
-
-
facilitation of bacterial sulfate uptake by Rv1739c requires CysA and its associated sulfate permease activity, thus Rv1739c may be a CysTWA-dependent sulfate transporter
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-
?
additional information
?
-
-
facilitation of bacterial sulfate uptake by Rv1739c requires CysA and its associated sulfate permease activity, thus Rv1739c may be a CysTWA-dependent sulfate transporter
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-
?
additional information
?
-
-
Na+-independent sulfate uptake
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-
?
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NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
ATP + H2O + sulfate-[sulfate-binding protein][side 1]
ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1] + H+
ATP + H2O + sulfate/out
ADP + phosphate + sulfate/in
-
transport of sulfate and thiosulfate
-
?
ATP + H2O + thiosulfate/out
ADP + phosphate + thiosulfate/in
-
transport of sulfate and thiosulfate
-
?
ATP + H2O + sulfate-[sulfate-binding protein][side 1]
ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1] + H+
-
-
-
-
?
ATP + H2O + sulfate-[sulfate-binding protein][side 1]
ADP + phosphate + sulfate[side 2] + [sulfate-binding protein][side 1] + H+
-
-
-
-
?
additional information
?
-
-
facilitation of bacterial sulfate uptake by Rv1739c requires CysA and its associated sulfate permease activity, thus Rv1739c may be a CysTWA-dependent sulfate transporter
-
-
?
additional information
?
-
-
facilitation of bacterial sulfate uptake by Rv1739c requires CysA and its associated sulfate permease activity, thus Rv1739c may be a CysTWA-dependent sulfate transporter
-
-
?
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METALS and IONS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
additional information
-
no inhibition by bicarbonate, nitrate, or phosphate, or by the anion transport inhibitor NS3623
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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Adenocarcinoma
Loss of the SWI/SNF-ATPase subunit members SMARCF1 (ARID1A), SMARCA2 (BRM), SMARCA4 (BRG1) and SMARCB1 (INI1) in oesophageal adenocarcinoma.
Adenoma
Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea.
Bradycardia
ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia.
Carcinogenesis
BRG1 attenuates colonic inflammation and tumorigenesis through autophagy-dependent oxidative stress sequestration.
Carcinogenesis
BRG1 promotes the repair of DNA double-strand breaks by facilitating the replacement of RPA with RAD51.
Carcinoma
The ATPase subunit of ATP6V1C1 inhibits autophagy and enhances radiotherapy resistance in esophageal squamous cell carcinoma.
Cataract
Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress.
Choriocarcinoma
Altered mitochondrial gene expression in human gestational trophoblastic diseases.
Colonic Neoplasms
Epigenetic silencing of the sulfate transporter gene DTDST induces sialyl Lewisx expression and accelerates proliferation of colon cancer cells.
Colorectal Neoplasms
PRMT1-mediated H4R3me2a recruits SMARCA4 to promote colorectal cancer progression by enhancing EGFR signaling.
Cysts
Multilocus sequence analysis of Echinococcus granulosus strains isolated from humans and animals in Iran.
Deafness
Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress.
Dehydration
Drought-Enhanced Xylem Sap Sulfate Closes Stomata by Affecting ALMT12 and Guard Cell ABA Synthesis.
Dehydration
Re-examining the role of ABA as the primary long-distance signal produced by water-stressed roots.
Down Syndrome
Proteasome subunit proteins and neuropathology in tauopathies and synucleinopathies: Consequences for proteomic analyses.
Dystonia
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.
Esophageal Squamous Cell Carcinoma
The ATPase subunit of ATP6V1C1 inhibits autophagy and enhances radiotherapy resistance in esophageal squamous cell carcinoma.
Genetic Diseases, Inborn
Genetic Disorders of Membrane Transport III. Congenital chloride diarrhea.
Genetic Diseases, Inborn
Mitochondrial G8292A and C8794T mutations in patients with Niemann-Pick disease type C.
Gestational Trophoblastic Disease
Altered mitochondrial gene expression in human gestational trophoblastic diseases.
Hemiplegia
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.
Hepatoblastoma
Mitochondrial genome-encoded ATPase subunit 6+8 mRNA increases in human hepatoblastoma cells in response to nonfatal cold stress.
Hereditary Complement Deficiency Diseases
Identification and functional characterization of the sulfate transporter gene GmSULTR1;2b in soybean.
Hydatidiform Mole
Altered mitochondrial gene expression in human gestational trophoblastic diseases.
Hyperoxaluria
Absence of the sulfate transporter SAT-1 has no impact on oxalate handling by mouse intestine and does not cause hyperoxaluria or hyperoxalemia.
Ichthyosis, Lamellar
Keratinocyte ATP binding cassette transporter expression is regulated by ultraviolet light.
Infections
Analysis and identification of tyrosine phosphorylated proteins in hemocytes of Litopenaeus vannamei infected with WSSV.
Infertility, Male
Development of KASP marker for cytoplasmic male sterility in Nicotiana tabacum and utilization in trait introgression.
Infertility, Male
Genetic and cytological analysis of a new spontaneous male sterility in radish (Raphanus sativus L.)
Infertility, Male
Subunit 6 of the Fo-ATP synthase complex from cytoplasmic male-sterile radish: RNA editing and NH2-terminal protein sequencing.
Intestinal Volvulus
The mitochondrial genome of Onchocerca volvulus: sequence, structure and phylogenetic analysis.
Invasive Pulmonary Aspergillosis
Exploration of Sulfur Assimilation of Aspergillus fumigatus Reveals Biosynthesis of Sulfur-Containing Amino Acids as a Virulence Determinant.
Leukemia
Essential role of BRG, the ATPase subunit of BAF chromatin remodeling complexes, in leukemia maintenance.
Leukemia
Recombinant bovine interferon-? enhances in vitro development of bovine embryos by upregulating expression of connexin 43 and E-cadherin.
Leukemia
Role of SWI/SNF in acute leukemia maintenance and enhancer-mediated Myc regulation.
Lung Neoplasms
BRG1 Loss Predisposes Lung Cancers to Replicative Stress and ATR Dependency.
Mitochondrial Diseases
Reduced respiratory control with ADP and changed pattern of respiratory chain enzymes as a result of selective deficiency of the mitochondrial ATP synthase.
Movement Disorders
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.
Neoplasms
BRG1, the ATPase subunit of SWI/SNF chromatin remodeling complex, interacts with HDAC2 to modulate telomerase expression in human cancer cells.
Neoplasms
BRM: the core ATPase subunit of SWI/SNF chromatin-remodelling complex-a tumour suppressor or tumour-promoting factor?
Neoplasms
CHIP and BAP1 Act in Concert to Regulate INO80 Ubiquitination and Stability for DNA Replication.
Neoplasms
Epigenetic silencing of the sulfate transporter gene DTDST induces sialyl Lewisx expression and accelerates proliferation of colon cancer cells.
Neoplasms
Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.
Neoplasms
Inhibition of vacuolar ATPase subunit in tumor cells delays tumor growth by decreasing the essential macrophage population in the tumor microenvironment.
Neoplasms
Lactate inhibits ATP6V0d2 expression in tumor-associated macrophages to promote HIF-2?-mediated tumor progression.
Neoplasms
Lysosomotropic properties of weakly basic anticancer agents promote cancer cell selectivity in vitro.
Neoplasms
Manipulation of the ubiquitin-proteasome pathway in cachexia: pentoxifylline suppresses the activation of 20S and 26S proteasomes in muscles from tumor-bearing rats.
Neoplasms
Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression.
Neoplasms
Role of SWI/SNF in acute leukemia maintenance and enhancer-mediated Myc regulation.
Neoplasms
[Research Progress on the Role of Chromatin Remodeling Factor BRG1 in Acute Myeloid Leukemia].
Osteochondrodysplasias
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype.
Osteochondrodysplasias
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia.
Osteochondrodysplasias
Achondrogenesis type IB: agenesis of cartilage interterritorial matrix as the link between gene defect and pathological skeletal phenotype.
Osteochondrodysplasias
Autosomal recessive multiple epiphyseal dysplasia with homozygosity for C653S in the DTDST gene: double-layer patella as a reliable sign.
Osteochondrodysplasias
Diastrophic dysplasia: prenatal diagnosis and review of the literature.
Osteochondrodysplasias
Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans.
Osteochondrodysplasias
In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias.
Osteochondrodysplasias
Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed.
Osteochondrodysplasias
SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types.
Osteosarcoma
Identification of cellular proteins interacting with equine infectious anemia virus S2 protein.
Otosclerosis
Effect of 17 beta-estradiol on diastrophic dysplasia sulfate transporter activity in otosclerotic bone cell cultures and SaOS-2 cells.
Otosclerosis
Glucocorticoids inhibit diastrophic dysplasia sulfate transporter activity in otosclerosis by interleukin-6.
Otosclerosis
Increased activity of the diastrophic dysplasia sulfate transporter in otosclerosis and its inhibition by sodium fluoride.
Parkinsonian Disorders
Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.
Pediatric Obesity
Mitochondrial ATPase subunit 6 and cytochrome B gene variations in obese Turkish children.
Retinoblastoma
The crystal structure of gankyrin, an oncoprotein found in complexes with cyclin-dependent kinase 4, a 19 S proteasomal ATPase regulator, and the tumor suppressors Rb and p53.
Rhabdoid Tumor
Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.
Sarcoma
SMARCA4 inactivation defines a group of undifferentiated thoracic malignancies transcriptionally related to BAF-deficient sarcomas.
Seminoma
Reduced semen quality in patients with testicular cancer seminoma is associated with alterations in the expression of sperm proteins.
Skin Neoplasms
BRM and BRG1 subunits of the SWI/SNF chromatin remodelling complex are downregulated upon progression of benign skin lesions into invasive tumours.
Spondylolysis
Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene.
Starvation
Downregulation of ubiquitin-dependent proteolysis by eicosapentaenoic acid in acute starvation.
Starvation
Identification and functional characterization of a sulfate transporter induced by both sulfur starvation and mycorrhiza formation in Lotus japonicus.
Starvation
Regulation of sulfur assimilation in higher plants: a sulfate transporter induced in sulfate-starved roots plays a central role in Arabidopsis thaliana.
Tuberculosis
Guanine nucleotides differentially modulate backbone dynamics of the STAS domain of the SulP/SLC26 transport protein Rv1739c of Mycobacterium tuberculosis.
Tuberculosis
Increased sulfate uptake by E. coli overexpressing the SLC26-related SulP protein Rv1739c from Mycobacterium tuberculosis.
Tuberculosis
Induced Folding Under Membrane Mimetic and Acidic Conditions Implies Undiscovered Biological Roles of Prokaryotic Ubiquitin-Like Protein Pup.
Tuberculosis
NMR assignment and secondary structure of the STAS domain of Rv1739c, a putative sulfate transporter of Mycobacterium tuberculosis.
Tuberculosis
Solution Structure of the Guanine Nucleotide-binding STAS Domain of SLC26-related SulP Protein Rv1739c from Mycobacterium tuberculosis.
Ventricular Fibrillation
ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia.
Vitamin B 6 Deficiency
Effects of Pyridoxine Deficiency on Hippocampal Function and Its Possible Association with V-Type Proton ATPase Subunit B2 and Heat Shock Cognate Protein 70.
Wilms Tumor
BRG1-SWI/SNF-dependent regulation of the Wt1 transcriptional landscape mediates epicardial activity during heart development and disease.
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KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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pH RANGE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
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LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY
GeneOntology No.
LITERATURE
SOURCE
Show AA Sequence and Transmembrane Helices (5822 entries)
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SUBUNIT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
additional information
additional information
-
the ABC-transoprter consists of both the membrane components - the products of the genes cysT, cysW and cysA and the periplasmic binders - the products of the genes cysP and sbp
additional information
-
identification of the cysP gene product as a thiosulfate-binding protein
additional information
-
cysA encodes the membrane-associated ATP-binding protein, sbpA encodes the sulfate-binding protein, cysT and cysW encode proteins that may form a channel for the transport of sulfate across the cytoplasmic membrane, cysT encodes a polypeptide that has some homology to a family of prokaryotic regulatory proteins
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CRYSTALLIZATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
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PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
S129C/G46C
-
mutation in the periplasmic sulfate receptor, dissociation of sulfate from the mutant enzyme is very slow under oxidizing conditions and increases more than 200-fold when reducing agent is added. This effect is attributed to a loss of interdomain structural flexibility in the presence of the disulfide
additional information
additional information
-
mutation to serine of the three cysteine residues of Rv1739c does not affect magnitude, pH-dependence, or pharmacology of sulfate uptake
additional information
-
mutation to serine of the three cysteine residues of Rv1739c does not affect magnitude, pH-dependence, or pharmacology of sulfate uptake
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PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
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CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
inducible expression of Rv1739c in an Escherichia coli strain EWP44 lacking CysA does not increase sulfate uptake by intact cells. Expression of Rv1739c in a Mycobacterium bovis BCG strain lacking the ABC sulfate permease subunit CysA cannot complement sulfate auxotrophy. Induction of Rv1739c expression in Escherichia coli increases bacterial uptake of sulfate, but not Cl-, formate, or oxalate. Sulfate uptake is also increased by overexpression of the Rv1739c transmembrane domain, but not of the cytoplasmic C-terminal STAS domain
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REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Sirko, A.; Zatyka, M.; Sadowy, E.; Hulanicka, D.
Sulfate and thiosulfate transport in Escherichia coli K-12: evidence for a functional overlapping of sulfate- and thiosulfate-binding proteins
J. Bacteriol.
177
4134-4136
1995
Escherichia coli
brenda
Jacobson, B.L.; He, J.J.; Vermersch, P.S.; Lemon, D.D.; Quiocho, F.A.
Engineered interdomain disulfide in the perplasmic receptor for sulfate transport reduces flexibility. Site-directed mutagenesis and ligand-binding studies
J. Biol. Chem.
266
5220-5225
1991
Escherichia coli
brenda
Laudenbach, D.E.; Grossmann, A.R.
Characterization and mutagenesis of sulfur-regulated genes in a Cyanobacterium: evidence for function in sulfate transport
J. Bacteriol.
173
2739-2750
1991
Marchantia polymorpha, Synechococcus sp.
brenda
Hryniewicz, M.; Sirko, A.; Palucha, A.; Boeck, A.; Hulanicka, D.
Sulfate and thiosulfate transport in Escherichia coli K-12: identification of a gene encoding a novel protein involved in thiosulfate binding
J. Bacteriol.
172
3358-3366
1990
Escherichia coli
brenda
Scheffel, F.; Demmer, U.; Warkentin, E.; Huelsmann, A.; Schneider, E.; Ermler, U.
Structure of the ATPase subunit CysA of the putative sulfate ATP-binding cassette (ABC) transporter from Alicyclobacillus acidocaldarius
FEBS Lett.
579
2953-2958
2005
Alicyclobacillus acidocaldarius
brenda
Zolotarev, A.S.; Unnikrishnan, M.; Shmukler, B.E.; Clark, J.S.; Vandorpe, D.H.; Grigorieff, N.; Rubin, E.J.; Alper, S.L.
Increased sulfate uptake by E. coli overexpressing the SLC26-related SulP protein Rv1739c from Mycobacterium tuberculosis
Comp. Biochem. Physiol. A
149
255-266
2008
Mycobacterium tuberculosis, Mycobacterium tuberculosis H37Rv
brenda
Marietou, A.; Roy, H.; Jorgensen, B.B.; Kjeldsen, K.U.
Sulfate transporters in dissimilatory sulfate reducing microorganisms a comparative genomics analysis
Front. Microbiol.
9
309
2018
Bacillus subtilis, Corynebacterium glutamicum
brenda
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