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3'-Phosphoadenosine-5'-phosphosulfate

3'-Phosphoadenosine-5'-phosphosulfate (PAPS) is an activated sulfate donor molecule essential for biological sulfation reactions in various organisms, including eukaryotes and prokaryotes.^[1] Chemically, it is an adenosine-based nucleotide with phosphates at the 3' and 5' positions of the ribose ring, where the 5'-phosphate is linked to a sulfate group, giving it the molecular formula C₁₀H₁₅N₅O₁₃P₂S and a molar mass of 507.26 g/mol.^[2] PAPS is synthesized through a two-step enzymatic pathway that activates inorganic sulfate for transfer. In the first step, ATP sulfurylase (also known as sulfate adenylyltransferase) reacts ATP with sulfate to produce adenosine 5'-phosphosulfate (APS) and pyrophosphate (PPi). The second step involves APS kinase phosphorylating the 3'-hydroxyl group of APS using another ATP molecule to form PAPS and ADP. In humans and other mammals, these reactions are catalyzed by bifunctional enzymes called PAPS synthetases (PAPSS1 and PAPSS2), which contain distinct N-terminal APS kinase and C-terminal ATP sulfurylase domains connected by a flexible linker.^[1]^[3] As the universal sulfate donor, PAPS is utilized by sulfotransferase enzymes to transfer its sulfo group to a wide range of substrates, including proteins (e.g., tyrosine sulfation for signaling), carbohydrates (e.g., glycosaminoglycans in extracellular matrix), lipids, and small molecules like steroids and xenobiotics. This sulfation process is critical for detoxification, hormone bioactivation (such as estrogen sulfation), modulation of protein-protein interactions, and structural integrity of connective tissues. Dysregulation of PAPS biosynthesis, such as mutations in PAPSS genes, can lead to skeletal disorders and metabolic imbalances due to impaired sulfation.^[1]

Structure and properties

Chemical structure

3'-Phosphoadenosine-5'-phosphosulfate (PAPS) is a derivative of adenosine 5'-monophosphate (AMP), featuring an additional phosphate group linked via a phosphoester bond to the 3' position of the ribose moiety and a sulfate group attached to the 5'-phosphate through a mixed phosphoric-sulfuric anhydride bond.^[4]^[5] The systematic IUPAC name for PAPS is [({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]sulfonic acid.^[5] The molecular formula of PAPS is \ce{C10H15N5O13P2S}. Its core structure comprises an adenine nucleobase N-glycosidically bonded to the C1' of a β-D-ribofuranose sugar, with the 3'-phosphate forming a phosphoester to the C3' hydroxyl and the 5'-phosphosulfate consisting of the 5'-phosphate esterified to the sulfate via the anhydride linkage at the C5' methylene.^[4]^[6]

Physical and chemical properties

3'-Phosphoadenosine-5'-phosphosulfate (PAPS) has the molecular formula C₁₀H₁₅N₅O₁₃P₂S and a molar mass of 507.26 g/mol (free acid basis).^[7] In its isolated form, PAPS typically appears as an off-white crystalline powder.^[8] PAPS exhibits high solubility in water, dissolving at concentrations up to 50 mg/mL to form a clear, colorless to faintly yellow solution.^[9] This solubility arises from its ionic phosphate and sulfate groups, which confer polarity and hydrophilicity; conversely, it shows poor solubility in organic solvents due to these charged moieties.^[9] Regarding stability, PAPS is labile under acidic conditions, undergoing hydrolysis via elimination of sulfur trioxide to yield 3'-phosphoadenosine 5'-phosphate (PAP) and inorganic sulfate.^[10] It remains relatively stable at neutral pH, though non-enzymatic hydrolysis occurs gradually over time, necessitating storage of solutions at -70°C or below and preparation of fresh stocks for experimental use.^[9] The chemical reactivity of PAPS is dominated by its high-energy sulfate group, which functions as an activated sulfate donor in sulfation reactions.^[9] Spectral properties of PAPS include ultraviolet absorption at 259 nm with a molar extinction coefficient (ε) of 15.4 mM⁻¹ cm⁻¹ at pH 7.0, attributable to the adenine moiety and commonly exploited in quantitative assays.^[9]

Biosynthesis

Formation of adenosine 5'-phosphosulfate (APS)

The formation of adenosine 5'-phosphosulfate (APS) represents the primary activation of inorganic sulfate in sulfur metabolism, enabling its incorporation into biomolecules. This process is catalyzed by ATP sulfurylase (also termed sulfate adenylyltransferase), which transfers the adenylyl group from ATP to sulfate, yielding APS and inorganic pyrophosphate (PPi). The reaction is depicted as:

\ce{SO4^{2-} + ATP ⇌ APS + PPi}

This step creates a high-energy mixed anhydride bond in APS, facilitating subsequent sulfur transfer reactions. ATP sulfurylase is ubiquitous in sulfate-utilizing organisms, from prokaryotes to eukaryotes, underscoring its essential role in sulfur homeostasis.^[11] The enzymatic mechanism proceeds via an SN2-like nucleophilic substitution, where an oxygen atom from the sulfate ion performs an in-line attack on the α-phosphorus of ATP, resulting in inversion of configuration at that site and cleavage of the α-β phosphoanhydride bond. This transition state is stabilized by active-site residues that position the substrates, with no covalent enzyme intermediates formed. The reaction strictly requires Mg²⁺ as a cofactor, which binds to the β- and γ-phosphates of ATP, neutralizing their negative charges and promoting proper alignment for the attack while facilitating PPi release. In mammals, ATP sulfurylase comprises the C-terminal catalytic domain of bifunctional PAPS synthases (PAPSS1 and PAPSS2 in humans), integrating it with downstream APS phosphorylation. By contrast, prokaryotes and plants express it as a standalone enzyme, such as the heterodimeric CysD/CysN in Escherichia coli or the homotetrameric ATPS isoforms (e.g., ATPS1–4) in Arabidopsis thaliana, often localized to plastids or cytosol. In yeast such as Saccharomyces cerevisiae, it is a monofunctional enzyme encoded by the MET3 gene.^[12]^[13]^[14] Although thermodynamically reversible (with a free energy change near equilibrium), the forward reaction predominates in cellular contexts due to rapid PPi hydrolysis by inorganic pyrophosphatase, which irreversibly consumes PPi and pulls the equilibrium toward APS production. This coupling is critical for efficient sulfate activation, as uncoupled reactions favor ATP resynthesis. In animals, where dietary sulfur sources predominate over de novo assimilation, this step is particularly rate-limiting owing to low intracellular free sulfate concentrations (typically 0.1–0.3 mM), which constrain substrate availability and thus PAPS supply for sulfation pathways.^[15]^[3]

Formation of PAPS from APS

The formation of 3'-phosphoadenosine-5'-phosphosulfate (PAPS) represents the second and final step in the biosynthesis of this activated sulfate donor, where adenosine 5'-phosphosulfate (APS) is phosphorylated by adenosine triphosphate (ATP). This reaction, APS + ATP → PAPS + ADP, is catalyzed by APS kinase, also known as the APS kinase domain in bifunctional 3'-phosphoadenosine-5'-phosphosulfate synthases (PAPSS).^[3] In eukaryotes such as animals, APS kinase forms the N-terminal domain of bifunctional PAPSS enzymes, which integrate both APS formation and phosphorylation activities into a single polypeptide.^[3] In humans, two isoforms of the bifunctional PAPSS enzyme exist: PAPSS1 and PAPSS2. PAPSS1 is ubiquitously expressed, with particularly high levels in brain and skin, and exists primarily as a stable dimeric protein with an N-terminal APS kinase domain and a C-terminal ATP sulfurylase domain connected by a flexible linker.^[16]^[3] In contrast, PAPSS2 is predominantly expressed in liver, cartilage, and adrenal glands, where it supports sulfation processes critical for detoxification and skeletal development; it shares a similar dimeric structure but exhibits lower thermal stability, with a half-life of approximately 8 minutes at 37°C compared to over 8 minutes for PAPSS1.^[16]^[3] Both isoforms contain regulatory domains that influence activity, and their expression patterns reflect tissue-specific demands for PAPS in sulfotransferase reactions.^[17] The catalytic mechanism involves the ordered binding of substrates, with Mg²⁺-complexed ATP binding first to the enzyme's nucleotide-binding site, followed by APS. The γ-phosphate of ATP is then transferred to the 3'-hydroxyl group of the ribose in APS, facilitated by Mg²⁺ coordination of the active site residues (such as aspartates in the DGDN motif) and a water network that positions the 3'-OH for nucleophilic attack.^[18] This Mg²⁺-dependent phosphorylation yields PAPS and ADP, with product release occurring in the reverse order: PAPS first, then ADP-Mg²⁺.^[18] Crystal structures of APS kinase domains, including those from human PAPSS1, reveal a closed active-site conformation upon substrate binding, stabilizing the transition state.^[19] Regulation of APS kinase activity primarily occurs through product inhibition by PAPS, which acts as a competitive inhibitor with respect to APS (K_i values in the micromolar range) and non-competitive with ATP, thereby preventing overproduction of PAPS when sulfation demands are low.^[20] This feedback mechanism is complemented by tissue-specific expression, such as elevated PAPSS2 in the liver, where high PAPS levels support xenobiotic detoxification via sulfation.^[16] Additionally, substrate inhibition by excess APS can occur, binding to both ATP and APS sites to modulate activity based on cellular sulfate availability.^[21] Across organisms, the organization of APS kinase varies. In animals, it is integrated into bifunctional PAPSS enzymes, enabling coordinated sulfate activation.^[3] In bacteria, such as Escherichia coli, APS kinase is encoded by a separate gene, cysC, functioning as a monofunctional enzyme essential for sulfate assimilation into cysteine.^[22] Plants, including Arabidopsis thaliana, also feature monofunctional APS kinases (e.g., APK1 and APK2 isoforms), which are localized in plastids and cytosol to balance primary sulfate reduction and secondary sulfation pathways, with redox-sensitive cysteines providing additional regulation not seen in animal or bacterial counterparts.^[21]^[18]

Biological roles

Role in sulfation reactions

3'-Phosphoadenosine-5'-phosphosulfate (PAPS) serves as the universal sulfate donor in biological sulfation reactions, transferring its sulfate group to a variety of acceptor substrates in a process catalyzed by sulfotransferases.^[3] The general reaction involves PAPS reacting with an acceptor molecule, such as a tyrosine residue or a carbohydrate, to form a sulfated product and 3'-phosphoadenosine-5'-phosphate (PAP) as a by-product:

\text{PAPS} + \text{acceptor} \rightarrow \text{sulfated acceptor} + \text{PAP}

This sulfation is a key post-translational modification essential for modulating the function, localization, and stability of biomolecules.^[23]^[24] Sulfotransferases (SULTs) constitute a superfamily of enzymes that mediate these transfers, with over 40 isoforms identified across mammals, including 13 cytosolic isoforms in humans divided into families such as SULT1, SULT2, and SULT4.^[24]^[25] In mammals, specific isoforms exhibit distinct substrate preferences; for instance, human SULT1A1 primarily catalyzes the sulfation of small phenolic compounds, including environmental phenols and drugs like acetaminophen, while SULT2A1 targets steroid hormones such as dehydroepiandrosterone.^[26]^[27] Tyrosylprotein sulfotransferases (TPST1 and TPST2), which are Golgi-resident enzymes, specifically handle protein tyrosine sulfation using PAPS.^[28] Additionally, chondroitin 4-O-sulfotransferase and related enzymes utilize PAPS to sulfate glycosaminoglycans like chondroitin, contributing to extracellular matrix assembly.^[29] PAPS-dependent sulfation acts on diverse substrates, including proteins, carbohydrates, lipids, and small molecules, thereby influencing numerous physiological processes. In proteins, tyrosine sulfation enhances peptide-protein interactions critical for signaling pathways, such as in chemokine receptors and coagulation factors.^[30] Glycosaminoglycan sulfation, as in chondroitin sulfate, is vital for cartilage structure and tissue development.^[31] Lipid sulfation modulates membrane properties, while small molecule sulfation facilitates detoxification of xenobiotics and endogenous compounds like catecholamines.^[32] These reactions are biologically crucial for hormone regulation, neurotransmitter modulation, and xenobiotic clearance. For example, sulfation of thyroid hormones by SULT1A1 and SULT1C1 inactivates them, preventing excessive activity and aiding their excretion, which is essential for metabolic homeostasis.^[33]^[34] Neurotransmitter sulfation, such as of dopamine by SULT1A3, influences synaptic transmission and mood regulation.^[32] Defects in PAPS utilization or sulfotransferase activity lead to undersulfation, resulting in disorders like skeletal dysplasias (e.g., brachyolmia due to PAPSS2 mutations affecting PAPS supply) and impaired detoxification.^[35]^[36] The reaction product PAP acts as a potent inhibitor of sulfotransferases, binding to the enzyme's active site and reducing catalytic efficiency, which necessitates efficient PAPS regeneration pathways to sustain sulfation flux in cells.^[37] This inhibition underscores the importance of coupled biosynthetic systems that recycle PAP back to PAPS, preventing metabolic bottlenecks in sulfation-dependent processes.^[38]

Role in sulfate assimilation

In the reductive assimilation of sulfate, primarily occurring in plants, fungi, and bacteria, inorganic sulfate is activated and reduced to sulfite and subsequently sulfide, which is incorporated into organic sulfur compounds such as cysteine and methionine for protein synthesis and other metabolic needs.^[39] This pathway enables autotrophic organisms to acquire sulfur from environmental sources, contrasting with animals that lack it and rely on dietary sulfur-containing amino acids.^[40] While adenosine 5'-phosphosulfate (APS) serves as the primary activated intermediate in plants and some bacteria, 3'-phosphoadenosine-5'-phosphosulfate (PAPS) plays a central role in fungi and certain bacteria, where it undergoes reduction as part of the assimilatory process.^[41] The key step involving PAPS occurs in organisms such as fungi and enteric bacteria, where PAPS reductase catalyzes its reduction to sulfite, releasing 3'-phosphoadenosine-5'-phosphate (PAP) as a byproduct. This reaction is:

\text{PAPS} + 2e^- + 2H^+ \rightarrow \text{PAP} + \text{HSO}_3^-

^[42] The enzyme, often ferredoxin- or NADPH-dependent, transfers electrons to reduce the sulfate group in PAPS.^[43] In bacteria like Escherichia coli, this is mediated by the CysH protein, while in fungi such as Aspergillus terreus, it is encoded by genes like sAT.^[44] The resulting sulfite is then further reduced to sulfide (H₂S) by sulfite reductase, using ferredoxin or NADPH as electron donors, before sulfide combines with O-acetylserine to form cysteine via O-acetylserine(thiol)lyase.^[22] In plants, the assimilatory pathway predominantly utilizes APS reductase (APR), encoded by genes such as APR1, APR2, and APR3 in Arabidopsis thaliana, highlighting PAPS's more limited role in higher plants despite its structural suitability for reduction.^[40] This enzyme family shares sequence similarity with bacterial and fungal reductases but operates on APS to produce sulfite directly.^[45] The pathway is localized in plastids in photosynthetic organisms, ensuring efficient sulfur integration into primary metabolism.^[39] Variations exist across bacteria, where some species, including phototrophic ones, reduce APS directly using heterodimeric APS reductase complexes (AprA/B), bypassing PAPS phosphorylation.^[22] This assimilatory route contrasts with the dissimilatory sulfate reduction in anaerobic bacteria, which uses similar enzymes (e.g., AprBA) but generates H₂S for energy conservation rather than biosynthesis.^[46] In fungi, PAPS-dependent reduction remains essential for cytosolic sulfur assimilation, underscoring organism-specific adaptations to sulfur availability.^[44]

Metabolism

Reduction of PAPS

The reduction of 3'-phosphoadenosine-5'-phosphosulfate (PAPS) represents a pivotal enzymatic step in the assimilatory sulfate reduction pathway, primarily in bacteria such as Escherichia coli and certain archaea, where it facilitates the conversion of activated sulfate to sulfite for incorporation into sulfur-containing biomolecules like cysteine. This process is catalyzed by PAPS reductase, encoded by genes such as cysH in E. coli, which transforms PAPS into sulfite (SO₃²⁻) and adenosine 3',5'-bisphosphate (PAP). In some lower plants like mosses, analogous PAPS reductases contribute to sulfate assimilation, contrasting with the predominant use of APS reductase in higher plants.^[47]^[48] The primary reaction is a two-electron reduction, depicted as:

\text{PAPS} + 2e^- + 2H^+ \rightarrow \text{[PAP](/page/PAP)} + \text{HSO}_3^-

This is dependent on reduced thioredoxin (or glutaredoxin in some cases) as the immediate electron donor, with electrons ultimately derived from NADPH via thioredoxin reductase or from reduced ferredoxin in photosynthetic organisms. The mechanism proceeds via nucleophilic attack by a conserved active-site cysteine on the sulfur atom of PAPS, cleaving the S-O bond in the phosphosulfate moiety and forming a transient thiosulfonate or sulfocysteine intermediate. Subsequent electron transfer from thioredoxin reduces this intermediate, liberating sulfite and restoring the cysteine residue, often accompanied by conformational shifts in the enzyme between open and closed states to accommodate substrate binding and product release.^[49]^[50]^[51] PAPS reductases typically lack intrinsic iron-sulfur clusters, relying instead on external reductants, though related APS reductases in plants incorporate [4Fe-4S] clusters for direct ferredoxin interaction; the reaction exhibits pH dependence, with optimal activity around 8.0 in bacterial systems. This step integrates into the broader sulfate reduction pathway, enabling sulfur assimilation under nutrient-limited conditions. Gene expression of PAPS reductase is upregulated during sulfur limitation to boost pathway flux, ensuring adaptive responses to environmental sulfur availability.^[22]^[40]^[52]

Degradation pathways

The degradation of 3'-phosphoadenosine-5'-phosphosulfate (PAPS) primarily occurs through non-reductive hydrolysis, which cleaves phosphate bonds to regulate cellular levels of this activated sulfate donor and prevent toxic accumulation. In mammals, the enzyme 3'(2'),5'-bisphosphate nucleotidase 1 (BPNT1), a cytoplasmic 3'-nucleotidase, catalyzes the hydrolysis of PAPS to adenosine 5'-phosphosulfate (APS) and inorganic phosphate (Pi). This reaction reverses the final step of PAPS biosynthesis and is essential for sulfur homeostasis, with BPNT1 exhibiting specificity for the 3'-phosphate group on PAPS. Homologous enzymes in other organisms, such as CysQ in bacteria and SAL1 in plants, perform analogous functions, often with broader substrate specificity toward both PAPS and related nucleotides. In some species, nonspecific phosphatases contribute to this breakdown, ensuring efficient turnover under varying physiological conditions.^[53]^[54]^[55] The by-product of PAPS-dependent sulfation reactions, 3'-phosphoadenosine 5'-phosphate (PAP), undergoes further hydrolysis to AMP and Pi, facilitating adenosine recycling for nucleotide pools. This step is mediated by PAP phosphatases, including the cytoplasmic BPNT1 and the Golgi-localized IMPAD1 (also termed gPAPP or 3'(2'),5'-bisphosphate nucleotidase family member 1). IMPAD1 specifically targets PAP in the secretory pathway, preventing its buildup and supporting sulfation efficiency in glycosaminoglycan biosynthesis. These enzymatic activities ensure the complete salvage of the adenosine backbone, linking sulfate metabolism to broader purine nucleotide economy.^[56]^[54]^[57] In mammals, excess PAPS and its degradation products contribute to urinary sulfate excretion during sulfate overload, such as from high dietary sulfur intake, thereby maintaining systemic homeostasis. Daily urinary inorganic sulfate excretion is approximately 13 to 25 mmol per 24 hours in adults.^[58] Pathologically, degradation pathways are dysregulated in liver diseases; for example, in acetaminophen-induced acute liver failure, reduced PAPS synthesis due to decreased expression of PAPSS2 leads to PAPS depletion and undersulfation of proteins and lipids, exacerbating oxidative stress and tissue damage. Additionally, non-enzymatic hydrolysis of PAPS accelerates at low pH, as shown by pH-rate profiles indicating faster breakdown in acidic environments, which may occur in inflamed or ischemic tissues.^[59]^[60] Cellular regulation of PAPS levels involves nucleotide pyrophosphatase activity, which hydrolyzes pyrophosphate bonds in related nucleotides to limit PAPS buildup and coordinate with sulfate assimilation. Enzymes like those in the nucleotide pyrophosphatase/phosphodiesterase (NPP) family indirectly support this by degrading ATP-derived intermediates, ensuring balanced flux through the pathway without redox involvement.^[54]^[61]

Physiological and clinical significance

Occurrence and roles across organisms

3'-Phosphoadenosine-5'-phosphosulfate (PAPS) serves as the universal activated sulfate donor for sulfation reactions across diverse organisms, with its roles varying by kingdom due to evolutionary adaptations in sulfur metabolism.^[62] In animals, PAPS is synthesized in the cytosol by bifunctional PAPS synthases and subsequently transported into the Golgi lumen via specific transporters for sulfation processes.^[63] Its primary function is sulfation, including the modification of proteoglycans such as heparan sulfate, which is essential for extracellular matrix integrity in tissues like cartilage.^[63] In the liver, PAPS supports the conjugation of hormones, such as estrogens, by cytosolic sulfotransferases, facilitating detoxification and excretion of bioactive compounds.^[64] In plants, PAPS plays a dual role in both sulfation and sulfur assimilation pathways, with synthesis occurring predominantly in plastids, including chloroplasts.^[65] For sulfation, it donates sulfate to secondary metabolites like flavonoids, enhancing their solubility and potentially aiding in stress responses and pigmentation.^[66] In sulfur assimilation, adenosine 5'-phosphosulfate (APS) is the main intermediate reduced to sulfite in chloroplasts for cysteine biosynthesis.^[65] In bacteria and fungi, PAPS predominantly supports assimilatory sulfate reduction, where it is reduced to sulfite by PAPS reductases to provide reduced sulfur for cysteine and methionine synthesis.^[3] The PAPS synthesis pathway is evolutionarily conserved from bacteria to eukaryotes, reflecting its ancient origin in prokaryotic sulfur metabolism.^[67] However, animals have lost the genes for assimilatory sulfate reduction, such as those encoding PAPS reductases, shifting reliance to dietary sulfur amino acids while retaining PAPS exclusively for sulfation.^[67] In mammals, PAPS-related enzymes exhibit high expression in specific tissues, including the liver for detoxification of xenobiotics and hormones, the brain for neuromodulatory sulfation in signaling pathways, and gonads for steroid hormone metabolism.^[68]

Genetic deficiencies and diseases

Mutations in the PAPSS2 gene, which encodes 3'-phosphoadenosine-5'-phosphosulfate synthetase 2, lead to autosomal recessive disorders characterized by impaired sulfate activation and consequent undersulfation of biomolecules. Biallelic loss-of-function variants in PAPSS2 cause spondyloepimetaphyseal dysplasia (SEMD) or the related condition brachyolmia, manifesting as short-trunk short stature evident in childhood, platyspondyly with irregular vertebral endplates, precocious calcification of rib cartilage, and variable epiphyseal or metaphyseal changes in long bones such as shortened femoral necks and mild metacarpal shortening.^[69] Recent analyses indicate that skeletal abnormalities are invariably present in PAPSS2 deficiency, while androgen excess is observed less frequently.^[70] These skeletal abnormalities arise from deficient sulfation of cartilage proteoglycans, disrupting extracellular matrix integrity and bone development.^[69] Additionally, PAPSS2 mutations are associated with androgen excess due to impaired sulfation of dehydroepiandrosterone (DHEA), resulting in elevated levels of active androgens like androstenedione and testosterone, low dehydroepiandrosterone sulfate (DHEAS), premature pubarche, acne, hirsutism, and potential progression to polycystic ovary syndrome features in affected individuals.^[71]^[72] Variants in the PAPSS1 gene, encoding the ubiquitously expressed 3'-phosphoadenosine-5'-phosphosulfate synthetase 1 isoform, have been linked to altered sulfation pathways with clinical implications beyond skeletal effects. While PAPSS1 can partially compensate for PAPSS2 loss in some tissues, specific disruptions in PAPSS1 function contribute to androgen-related phenotypes through reduced DHEA sulfation, exacerbating conditions like acne and hyperandrogenism in contexts of hormonal imbalance.^[73] In oncology, knockdown of PAPSS1 in non-small cell lung cancer (NSCLC) cells sensitizes them to DNA-damaging agents such as cisplatin, radiation, and topoisomerase inhibitors by increasing DNA double-strand breaks, G1/S cell cycle arrest, and apoptosis, without affecting normal cells, suggesting a role in tumor resistance mechanisms via sulfation-dependent DNA repair or drug metabolism.^[74] Deficiencies in PAPSS1 and PAPSS2 also impair broader sulfation-dependent detoxification processes, as PAPS is essential for sulfonation of xenobiotics, hormones, and neurotransmitters by sulfotransferases, potentially leading to accumulation of unsulfated toxins and increased susceptibility to environmental or metabolic stressors.^[75] Diagnosis of PAPSS-related disorders typically involves genetic sequencing to identify biallelic variants in PAPSS1 or PAPSS2, complemented by biochemical assays showing low serum DHEAS, elevated urinary androsterone or other androgen metabolites, and increased plasma androgens.^[71]^[69] Treatment remains symptomatic, focusing on managing skeletal deformities through orthopedic interventions or androgen excess with anti-androgens, as inorganic sulfate supplementation fails to restore PAPS production due to the enzymatic block in sulfate activation.^[72]

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[36]
Sulfation of iodothyronines by human sulfotransferase 1C1 (SULT1C1)
Sulfation is an important component of human thyroid hormone metabolism. The role of the human sulfotransferase 1C1 (SULT1C1) is not known.
[37]
Skeletal Dysplasias Caused by Sulfation Defects - PMC
Apr 14, 2020 · PAPS represents the universal sulfate donor and is used by cytosolic sulfotransferases (SULTs) for hormone and xenobiotics sulfation or by Golgi ...
[38]
Bone and connective tissue disorders caused by defects in ...
Jul 8, 2019 · The defect causes PAPSS2 impairment leading to low intracellular levels of PAPS and consequently reduced sulfation of macromolecules. This ...
[39]
Phosphosulfate Allosterically Regulates Sulfotransferase Turnover
Oct 14, 2014 · ... structure responds to substrates and mediates their interactions. The binding of 3'-phosphoadenosine 5'-phosphosulfate (PAPS) gates access ...
[40]
[PDF] Regeneration of PAPS for the Enzymatic Synthesis of Sulfated ...
PAPS, the major obstacle to enzymatic synthesis with sulfotransferases is the complication of product inhibition by PAP, even in low micromolar concentrations.
[41]
Sulfate assimilation in eukaryotes: fusions, relocations and lateral ...
Feb 4, 2008 · The sulfate assimilation pathway is present in photosynthetic organisms, fungi, and many bacteria, providing reduced sulfur for the synthesis of cysteine and ...
[42]
Plant adenosine 5′-phosphosulphate reductase - Oxford Academic
Although, as discussed above, it was long believed that heterotrophic bacteria reduce sulphate via PAPS, an APS-dependent sulphate assimilation was confirmed ...
[43]
Control of sulfur partitioning between primary and secondary ...
Jul 18, 2012 · APS can either be reduced by APS reductase to sulfite in the primary sulfate assimilation pathway, or it can be phosphorylated by APS kinase to ...
[44]
Structural basis and evolution of redox regulation in plant adenosine-5
Dec 19, 2011 · In yeast, fungi, and enterobacteria, including Escherichia coli, sulfate is incorporated into adenosine-5′-phosphate (APS), then converted to 3′ ...
[45]
analysis of genes encoding ATP-sulfurylase and PAPS-reductase
Two genes for the sulfate assimilation pathway in Aspergillus terreus were cloned. The genes sAT (coding for PAPS-reductase) and sCT (coding for ATP-sulfur.<|separator|>
[46]
Molecular mechanisms of regulation of sulfate assimilation - Frontiers
APS is a branching point in sulfate assimilation, which can proceed by reduction to sulfite catalyzed by APS reductase or by phosphorylation to 3′- ...Abstract · Introduction · Control of Flux Through the... · Transcriptional Regulation
[47]
Assimilatory sulfate reduction in the marine methanogen ... - Nature
Jun 5, 2023 · A non-canonical PAP phosphatase then hydrolyses PAP. Finally, the F420-dependent sulfite reductase converts sulfite to sulfide for cellular ...
[48]
cysH - Phosphoadenosine 5'-phosphosulfate reductase | UniProtKB
The open, reduced form of PAPS reductase is able to bind PAPS, whereas the closed oxidized form cannot. A movement between the two monomers of the dimer may ...Missing: mechanism | Show results with:mechanism
[49]
Phosphoadenosine-5′-phosphosulfate Reductase Is a Novel Form ...
On the other hand, the PAPS-dependent activity of PpAPR-B showed a clear optimum at pH 8 (Fig. 7B). To test whether PpAPR or AtAPR might be capable of PAPS ...
[50]
3′-Phosphoadenosine-5′-phosphosulfate Reductase in Complex ...
Here we describe the structure of E. coli PAPS reductase in complex with E. coli Trx1, a key intermediate present during the catalytic cycle, at a resolution of ...
[51]
Reaction Mechanism of Thioredoxin: 3′‐Phospho‐adenylylsulfate ...
Properties of purified recombinant adenosine 3′-phosphate 5′-phosphosulfate (PAdoPS) reductase from Escherichia coli were investigated.
[52]
M-CSA Mechanism and Catalytic Site Atlas
Requiring thioredoxin as an electron donor, phosphoadenosine phosphosulphate reductase (CysH) catalyses the reduction of phosphoadenosine phosphosulphate (PAPS ...
[53]
Sulfur Regulation of the Sulfate Transporter Genes sutA and sutB in ...
The sulfate assimilation pathway catalyzes the uptake and reduction of sulfate, yielding sulfide that is incorporated into Cys. PAPS reductase reduces the ...
[54]
BPNT1 - 3'(2'),5'-bisphosphate nucleotidase 1 | UniProtKB - UniProt
Is also able to hydrolyze adenosine 3'-phosphate 5'-phosphosulfate (PAPS) to adenosine 5'-phosphosulfate (APS) (By similarity). Probably prevents the toxic ...
[55]
Roles for nucleotide phosphatases in sulfate assimilation and ... - NIH
In this review we provide an overview ... Sulfation and sulfotransferases 5: the importance of 3'-phosphoadenosine 5'-phosphosulfate (PAPS) in the regulation of ...
[56]
Sulfate/Sulfite Metabolism - SMPDB
APS is converted to phosphoadenylyl-sulfate (PAPS) via adenylylsulfate kinase. APS can also be regenerated from PAPS by 3'(2'), 5'-bisphosphate nucleotidase 1.
[57]
IMPAD1 hydrolyses PAP to AMP - Reactome
PAP is degraded to 5′-AMP (AMP) by 3′-nucleotidase family. Mammals encode two 3′-nucleotidases, the Golgi-resident inositol monophosphatase 3 (IMPAD3 aka PAP ...
[58]
Role for cytoplasmic nucleotide hydrolysis in hepatic function and ...
Mar 11, 2013 · In mice, Papps2 encodes a dual functional enzyme with both ATP sulfurylase and APS kinase activities that synthesize PAPS from sulfate and ATP.
[59]
[PDF] Test Definition: SULFU - Mayo Clinic Laboratories
Urinary sulfate is a reflection of dietary protein intake, particularly of meat, and thus can be used as an index of nutritional protein intake. It also is used ...Missing: excess mammals
[60]
Inhibition of p53 Sulfoconjugation Prevents Oxidative Hepatotoxicity ...
The expression of PAPSS2 is decreased in acetaminophen-induced acute liver failure. Knockout of Papss2 or inhibition of sulfation prevents acetaminophen ...
[61]
Adenosine-5'-phosphosulfate--a multifaceted modulator of ... - PubMed
For the APS kinase domain that phosphorylates APS to PAPS, APS is an uncompetitive substrate inhibitor that can bind both at the ATP/ADP-binding site and ...Missing: biosynthesis | Show results with:biosynthesis
[62]
Identification and Characterization of Inorganic Pyrophosphatase ...
In the latter reaction, PAPS enters the reductive sulfate assimilation pathway involving PAPS reductase ... The optimum pH was found to be 7.0, and the ...
[63]
Essential roles of 3'-phosphoadenosine 5'-phosphosulfate synthase ...
Apr 21, 2006 · All sulfation reactions in all organisms require activated sulfate, 3'-phosphoadenosine 5'-phosphosulfate (PAPS), as a universal donor.Missing: occurrence plants fungi evolution
[64]
Phosphosulfate Transporters Play Distinct Roles in Heparan Sulfate ...
For sulfation to occur, PAPS must pass through the Golgi membrane, which ... PAPS transporters transport PAPS from the cytosol into the Golgi lumen (16).Missing: hormones | Show results with:hormones
[65]
Sulfonation, an underexploited area: from skeletal development to ...
Aug 23, 2016 · Some, PAPSS2 mutations can lead to brachyolmia or more severe skeletal disorders such as spondyloepimetaphyseal dysplasia Pakisani type, ...
[66]
Chloroplastic Phosphoadenosine Phosphosulfate Metabolism ... - NIH
Chloroplasts are the sites of S reduction and the synthesis of Cys and subsequently GSH through a pathway that uses APS as a key intermediate (Kopriva, 2006).Missing: flavonoids | Show results with:flavonoids
[67]
Identification of a novel flavonoid glycoside sulfotransferase in ...
Sulfation of flavonoids is mediated by cytosolic sulfotransferases (SULTs), which utilize 3'-phosphoadenosine 5'-phosphosulfate (PAPS) as the sulfate donor.
[68]
Enzymatic basis for assimilatory and dissimilatory sulfate reduction
Assimilatory sulfate reducers reduced sulfate in the form of PAPS, and, with one exception, APS-reductase was found only in dissimilatory sulfate reducers. APS ...Missing: fungi: | Show results with:fungi:
[69]
Sulfation pathways from red to green - PMC - PubMed Central
These so-called PAPS synthases are strictly conserved within animal genomes with a single gene in invertebrates and a PAPSS1 and PAPSS2 gene pair in vertebrates ...
[70]
Sulfonation and Molecular Action | Endocrine Reviews
Sulfotransferases can be divided into two classes based upon whether they are soluble or membrane-associated proteins. Soluble or cytosolic sulfotransferases ...
[71]
PAPSS2 mutations cause autosomal recessive brachyolmia - PubMed
Jul 11, 2012 · PAPSS2 mutations have produced a skeletal dysplasia family, with a gradation of phenotypes ranging from brachyolmia to spondylo-epi-metaphyseal ...
[72]
Inactivating PAPSS2 Mutations in a Patient with Premature Pubarche
May 28, 2009 · ... DHEA sulfation increases the DHEA pool available for conversion to active androgens, thus causing androgen excess. These findings raise ...
[73]
PAPSS2 Deficiency Causes Androgen Excess via Impaired DHEA ...
Here we have studied the biochemical and clinical consequences of PAPSS2 deficiency in a family with two brothers compound heterozygous for two novel PAPSS2 ...
[74]
11-Oxygenated androgens in health and disease - PMC
Deficiency of PAPSS2 prevents DHEA sulfonation and leads to adrenal androgen excess ... acne, and they typically initiate around age 6–8 years in both boys ...
[75]
phosphosulfate synthase 1 (PAPSS1) knockdown sensitizes non ...
Jul 10, 2015 · Our study demonstrates for the first time that PAPSS1 could be targeted to improve the activity of multiple anticancer agents used to treat NSCLC.<|separator|>
[76]
The Role of Sulfotransferases in Liver Diseases - PubMed Central
This review is aimed to summarize the central role of major SULTs, including the SULT1 and SULT2 subfamilies, in the pathophysiology of liver and liver-related ...Missing: degradation undersulfation