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Two bifunctional inositol pyrophosphate kinases/phosphatases control plant phosphate homeostasis

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/anie.201301092openalex-snapshot

Synthesis of Unsymmetric Diphospho‐Inositol Polyphosphates

inferredcites →https://doi.org/10.1002/bimj.200810425openalex-snapshot

Simultaneous Inference in General Parametric Models

inferredcites →https://doi.org/10.1002/jcp.26017openalex-snapshot

Intimate connections: Inositol pyrophosphates at the interface of metabolic regulation and cell signaling

inferredcites →https://doi.org/10.1002/sim.6048openalex-snapshot

Testing for qualitative interaction using ratios of treatment differences

inferredcites →https://doi.org/10.1016/0003-2697(88)90484-8openalex-snapshot

A malachite green procedure for orthophosphate determination and its use in alkaline phosphatase-based enzyme immunoassay

inferredcites →https://doi.org/10.1016/0076-6879(66)08014-5openalex-snapshot

[10] Assay of inorganic phosphate, total phosphate and phosphatases

inferredcites →https://doi.org/10.1016/j.copbio.2017.08.012openalex-snapshot

Control of plant phosphate homeostasis by inositol pyrophosphates and the SPX domain

inferredcites →https://doi.org/10.1016/j.jbior.2016.10.003openalex-snapshot

The significance of the 1-kinase/1-phosphatase activities of the PPIP5K family

inferredcites →https://doi.org/10.1016/j.jmb.2017.12.007openalex-snapshot

A Completely Reimplemented MPI Bioinformatics Toolkit with a New HHpred Server at its Core

inferredcites →https://doi.org/10.1016/j.pbi.2017.05.007openalex-snapshot

Novel signals in the regulation of Pi starvation responses in plants: facts and promises

inferredcites →https://doi.org/10.1016/j.tibs.2016.10.008openalex-snapshot

Eukaryotic Phosphate Homeostasis: The Inositol Pyrophosphate Perspective

inferredcites →https://doi.org/10.1016/s0960-9822(00)80055-xopenalex-snapshot

Synthesis of diphosphoinositol pentakisphosphate by a newly identified family of higher inositol polyphosphate kinases

inferredcites →https://doi.org/10.1021/acs.biochem.5b00532openalex-snapshot

Asp1 from Schizosaccharomyces pombe Binds a [2Fe-2S]2+ Cluster Which Inhibits Inositol Pyrophosphate 1-Phosphatase Activity

inferredcites →https://doi.org/10.1021/acschembio.7b00026openalex-snapshot

Inositol Pyrophosphate Specificity of the SPX-Dependent Polyphosphate Polymerase VTC

inferredcites →https://doi.org/10.1038/nature05731openalex-snapshot

Mechanism of auxin perception by the TIR1 ubiquitin ligase

inferredcites →https://doi.org/10.1038/nature09430openalex-snapshot

Jasmonate perception by inositol-phosphate-potentiated COI1–JAZ co-receptor

inferredcites →https://doi.org/10.1038/nchembio.733openalex-snapshot

Structural basis for an inositol pyrophosphate kinase surmounting phosphate crowding

inferredcites →https://doi.org/10.1038/ncomms11095openalex-snapshot

Identification of plant vacuolar transporters mediating phosphate storage

inferredcites →https://doi.org/10.1038/ng.3289openalex-snapshot

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

inferredcites →https://doi.org/10.1039/c2sc21553eopenalex-snapshot

Synthesis and characterization of non-hydrolysable diphosphoinositol polyphosphate messengers

inferredcites →https://doi.org/10.1042/bcj20170522openalex-snapshot

AtSPX1 affects the AtPHR1–DNA-binding equilibrium by binding monomeric AtPHR1 in solution

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot

Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana

inferredcites →https://doi.org/10.1073/pnas.1404654111openalex-snapshot

SPX1 is a phosphate-dependent inhibitor of PHOSPHATE STARVATION RESPONSE 1 in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.1404680111openalex-snapshot

Rice SPX1 and SPX2 inhibit phosphate starvation responses through interacting with PHR2 in a phosphate-dependent manner

inferredcites →https://doi.org/10.1073/pnas.1514598112openalex-snapshot

A vacuolar phosphate transporter essential for phosphate homeostasis in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.1606853113openalex-snapshot

Inositol polyphosphates intersect with signaling and metabolic networks via two distinct mechanisms

inferredcites →https://doi.org/10.1073/pnas.1702370114openalex-snapshot

KO of 5-InsP 7 kinase activity transforms the HCT116 colon cancer cell line into a hypermetabolic, growth-inhibited phenotype

inferredcites →https://doi.org/10.1074/jbc.m111.266320openalex-snapshot

Identification of an Evolutionarily Conserved Family of Inorganic Polyphosphate Endopolyphosphatases

inferredcites →https://doi.org/10.1074/jbc.m116.765743openalex-snapshot

The Significance of the Bifunctional Kinase/Phosphatase Activities of Diphosphoinositol Pentakisphosphate Kinases (PPIP5Ks) for Coupling Inositol Pyrophosphate Cell Signaling to Cellular Phosphate Homeostasis

inferredcites →https://doi.org/10.1074/jbc.m704655200openalex-snapshot

Purification, Sequencing, and Molecular Identification of a Mammalian PP-InsP5 Kinase That Is Activated When Cells Are Exposed to Hyperosmotic Stress

inferredcites →https://doi.org/10.1074/jbc.m704656200openalex-snapshot

Cloning and Characterization of Two Human VIP1-like Inositol Hexakisphosphate and Diphosphoinositol Pentakisphosphate Kinases

inferredcites →https://doi.org/10.1074/jbc.m805686200openalex-snapshot

Structural Analysis and Detection of Biological Inositol Pyrophosphates Reveal That the Family of VIP/Diphosphoinositol Pentakisphosphate Kinases Are 1/3-Kinases

inferredcites →https://doi.org/10.1074/jbc.ra118.005884openalex-snapshot

5-Diphosphoinositol pentakisphosphate (5-IP7) regulates phosphate release from acidocalcisomes and yeast vacuoles

inferredcites →https://doi.org/10.1080/01621459.1955.10501294openalex-snapshot

A Multiple Comparison Procedure for Comparing Several Treatments with a Control

inferredcites →https://doi.org/10.1101/gad.204401openalex-snapshot

A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae

inferredcites →https://doi.org/10.1104/pp.103.027979openalex-snapshot

A Gateway Cloning Vector Set for High-Throughput Functional Analysis of Genes in Planta

inferredcites →https://doi.org/10.1104/pp.15.01336openalex-snapshot

Arabidopsis PHL2 and PHR1 Act Redundantly as the Key Components of the Central Regulatory System Controlling Transcriptional Responses to Phosphate Starvation

inferredcites →https://doi.org/10.1104/pp.16.00694openalex-snapshot

Inositol Polyphosphate Binding Specificity of the Jasmonate Receptor Complex

inferredcites →https://doi.org/10.1105/tpc.000745openalex-snapshot

Identification and Characterization of the Arabidopsis PHO1 Gene Involved in Phosphate Loading to the Xylem

inferredcites →https://doi.org/10.1105/tpc.113.120311openalex-snapshot

NITROGEN LIMITATION ADAPTATION Recruits PHOSPHATE2 to Target the Phosphate Transporter PT2 for Degradation during the Regulation of Arabidopsis Phosphate Homeostasis

inferredcites →https://doi.org/10.1105/tpc.114.135160openalex-snapshot

VIH2 Regulates the Synthesis of Inositol Pyrophosphate InsP8 and Jasmonate-Dependent Defenses in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.16.00351openalex-snapshot

Synergism between Inositol Polyphosphates and TOR Kinase Signaling in Nutrient Sensing, Growth Control, and Lipid Metabolism in Chlamydomonas

inferredcites →https://doi.org/10.1111/j.1365-313x.2008.03460.xopenalex-snapshot

Characterization of a sub‐family of Arabidopsis genes with the SPX domain reveals their diverse functions in plant tolerance to phosphorus starvation

inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04480.xopenalex-snapshot

Jasmonic acid perception by COI1 involves inositol polyphosphates in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1469-8137.2011.04002.xopenalex-snapshot

The emerging importance of the SPX domain‐containing proteins in phosphate homeostasis

inferredcites →https://doi.org/10.1111/tpj.12650openalex-snapshot

Arabidopsis inositol pentakisphosphate 2‐kinase, A t IPK 1, is required for growth and modulates phosphate homeostasis at the transcriptional level

inferredcites →https://doi.org/10.1111/tpj.12669openalex-snapshot

Two inositol hexakisphosphate kinases drive inositol pyrophosphate synthesis in plants

inferredcites →https://doi.org/10.1111/tpj.13974openalex-snapshot

Arabidopsis inositol phosphate kinases IPK 1 and ITPK 1 constitute a metabolic pathway in maintaining phosphate homeostasis

inferredcites →https://doi.org/10.1126/science.1139099openalex-snapshot

A Conserved Family of Enzymes That Phosphorylate Inositol Hexakisphosphate

inferredcites →https://doi.org/10.1126/science.1168120openalex-snapshot

Catalytic Core of a Membrane-Associated Eukaryotic Polyphosphate Polymerase

inferredcites →https://doi.org/10.1126/science.aad9858openalex-snapshot

Control of eukaryotic phosphate homeostasis by inositol polyphosphate sensor domains

inferredcites →https://doi.org/10.1128/mcb.00047-18openalex-snapshot

Asp1 Bifunctional Activity Modulates Spindle Function via Controlling Cellular Inositol Pyrophosphate Levels in Schizosaccharomyces pombe

inferredcites →https://doi.org/10.1371/journal.pgen.1001102openalex-snapshot

A Central Regulatory System Largely Controls Transcriptional Activation and Repression Responses to Phosphate Starvation in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.pone.0005580openalex-snapshot

Inositol Pyrophosphates and Their Unique Metabolic Complexity: Analysis by Gel Electrophoresis

inferredcites →https://doi.org/10.1371/journal.pone.0009788openalex-snapshot

A Robust Procedure for Comparing Multiple Means under Heteroscedasticity in Unbalanced Designs

inferredcites →https://doi.org/10.1371/journal.pone.0176085openalex-snapshot

A systematic genetic screen for genes involved in sensing inorganic phosphate availability in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.2307/2528930openalex-snapshot

A Test for Differences between Treatment Means When Several Dose Levels are Compared with a Zero Dose Control

inferredcites →https://doi.org/10.2307/2530666openalex-snapshot

Testing the Statistical Certainty of a Response to Increasing Doses of a Drug

inferredcites →https://doi.org/10.3389/fpls.2018.01432openalex-snapshot

Functional Characterization of Arabidopsis PHL4 in Plant Response to Phosphate Starvation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4766567openalex-extracted

Egphl7, Egphr1 and Egphr2 Bind to P1bs and a Unique Motif, Agatwc, for Phosphate Starvation Transcriptional Regulation in Oil Palm

inferred← citeshttps://doi.org/10.1016/j.jbiotec.2020.10.001openalex-snapshot

Transcriptional regulators of nitrate metabolism: Key players in improving nitrogen use in crops

inferred← citeshttps://doi.org/10.1016/j.jgg.2025.08.008openalex-snapshot

The interplay between phosphorus nutrition and abiotic stresses in plants

inferred← citeshttps://doi.org/10.1038/s41467-022-29275-8openalex-snapshot

Mechanistic insights into the regulation of plant phosphate homeostasis by the rice SPX2 – PHR2 complex

inferred← citeshttps://doi.org/10.1038/s41467-025-59331-yopenalex-snapshot

N 6-methyladenosine modifications stabilize phosphate starvation response–related mRNAs in plant adaptation to nutrient-deficient stress

inferred← citeshttps://doi.org/10.1038/s41598-020-72985-6openalex-snapshot

Systemic induction of phosphatidylinositol-based signaling in leaves of arbuscular mycorrhizal rice plants

inferred← citeshttps://doi.org/10.1038/s41598-022-13709-wopenalex-snapshot

Comparative transcriptome analysis reveals a rapid response to phosphorus deficiency in a phosphorus-efficient rice genotype

inferred← citeshttps://doi.org/10.1111/tpj.14642openalex-snapshot

A genetically validated approach for detecting inorganic polyphosphates in plants

inferred← citeshttps://doi.org/10.1371/journal.pgen.1011838openalex-snapshot

Conservation of heat stress acclimation by the IPK2-type kinases that control the synthesis of the inositol pyrophosphate 4/6-InsP7 in land plants

inferred← citeshttps://doi.org/10.20944/preprints202306.0686.v1openalex-snapshot

Molecular Regulation for Maintenance of Plant Phosphate Homeostasis in Crop Plants as Basis for Precision Genome Engineering

inferred← citeshttps://doi.org/10.3410/f.738775517.793583087openalex-snapshot

Faculty Opinions recommendation of Spatial profiles of phosphate in roots indicate developmental control of uptake, recycling, and sequestration.

inferred← citeshttps://doi.org/10.7554/elife.87956.2openalex-snapshot

Inositol Pyrophosphate Dynamics Reveals Control of the Yeast Phosphate Starvation Program Through 1,5-IP8 and the SPX Domain of Pho81

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