Cited by 110Protein Kinase Regulation and GTPase SignalingCalcium signaling and nucleotide metabolismPI3K/AKT/mTOR signaling in cancer

Mammalian inositol polyphosphate multikinase synthesizes inositol 1,4,5-trisphosphate and an inositol pyrophosphate

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Saiardi, Adolfo, Nagata, Eiichiro, Luo, Hongbo R., Sawa, Akira, Luo, Xiaojiang, Snowman, Adele M., Snyder, Solomon H.·2001·Proceedings of the National Academy of Sciences

Abstract

Using a consensus sequence in inositol phosphate kinase, we have identified and cloned a 44-kDa mammalian inositol phosphate kinase with broader catalytic capacities than any other member of the family and which we designate mammalian inositol phosphate multikinase (mIPMK). By phosphorylating inositol 4,5-bisphosphate, mIPMK provides an alternative biosynthesis for inositol 1,4,5-trisphosphate [Ins(1,4,5) P 3 ]. mIPMK also can form the pyrophosphate disphosphoinositol tetrakisphosphate (PP-Ins P 4 ) from Ins P 5 . Additionally, mIPMK forms Ins P 4 from Ins(1,4,5) P 3 and Ins P 5 from Ins(1,3,4,5) P 4 .

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Crossref · 10.1073/pnas.041614598

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  • IPMK, the mammalian homologue of Arg82, has been reported to phosphorylate Ins(1,4,5)P3 to form Ins(1,3,4,5,6)P4 and then Ins(1,3,4,5,6)P5.

    “IPMK, the mammalian homologue of Arg82, has been reported to phosphorylate Ins(1,4,5)P3 to form Ins(1,3,4,5,6)P4 and then Ins(1,3,4,5,6)P540,41.”

    From Structure of Hdac3 Bound to Co-Repressor and Inositol Tetraphosphate (2012) · cites this paper as [40]

    The Results (page unavailable) show that mammalian IPMK converts Ins(1,4,5)P3 to Ins(1,3,4,5)P4 and then to Ins(1,3,4,5,6)P5. The cited sentence gives the intermediate as Ins(1,3,4,5,6)P4, which is not the intermediate reported in the paper. (LLM, conf=0.90)

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Research works printed but not linked: 7

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Authors
Saiardi, A., Nagata, E., Luo, H. R., Sawa, A., Luo, X., Snowman, A. M., & Snyder, S. H.
Affiliations
Johns Hopkins University (US)
Corresponding author
Snyder, Solomon H.
Venue
Proceedings of the National Academy of Sciences
Published
2001-02-13
Volume
98
Issue
5
Pages
2306-2311
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W1997739014
Cited by
110
References
35
Citations by year
2026: 3 · 2025: 2 · 2024: 2 · 2022: 4 · 2021: 1 · 2020: 4 · 2019: 5 · 2018: 3 · 2017: 3 · 2016: 5 · 2015: 4 · 2014: 3 · 2013: 5 · 2012: 3
FWCI
2.56
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • UCL Discovery (University College London) (submittedVersion)
Funders
  • U.S. Public Health Service (MH‐18501, DA-00074)
  • National Institute of Mental Health (R01MH018501, R37MH018501, MH-18501)
  • National Institute on Drug Abuse (DA 00074, K05DA000074)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
Keywords
inositol polyphosphate multikinase, inositol 1,4,5-trisphosphate, inositol pyrophosphates, inositol 1,3,4,5-tetrakisphosphate, enzyme cloning, mammalian enzymes
MeSH terms
Amino Acid Sequence, Animals, Base Sequence, Cloning, Molecular, Male, Molecular Sequence Data, Inositol 1,4,5-Trisphosphate, Rats, Sprague-Dawley, Sequence Homology, Amino Acid, In Situ Hybridization, Phosphotransferases (Alcohol Group Acceptor), DNA Primers, Rats

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