Literature DB >> 27342751

Exploration of GGTase-I substrate requirements. Part 2: Synthesis and biochemical analysis of novel saturated geranylgeranyl diphosphate analogs.

Kayla J Temple1, Elia N Wright2, Carol A Fierke3, Richard A Gibbs4.   

Abstract

Protein prenylation is a type of post-translational modification that aids certain proteins in localizing to the plasma member where they activate cell signaling. To better understand the isoprenoid requirements and differences of FTase and GGTase-I, a series of saturated geranylgeranyl diphosphate analogs were synthesized and screened against both mammalian FTase and GGTase-I. Of our library of compounds, several analogs proved to be substrates of GGTase-I, with 11d having a krel=0.95 when compared to GGPP (krel=1.0).
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Farnesylation; Geranylgeranylation; Isoprenoid synthesis; Protein prenylation; Saturated GGPP analogs

Mesh:

Substances:

Year:  2016        PMID: 27342751      PMCID: PMC4955811          DOI: 10.1016/j.bmcl.2016.06.035

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  16 in total

Review 1.  Protein prenylation: a pivotal posttranslational process.

Authors:  Robert Roskoski
Journal:  Biochem Biophys Res Commun       Date:  2003-03-28       Impact factor: 3.575

Review 2.  Thematic review series: lipid posttranslational modifications. Structural biology of protein farnesyltransferase and geranylgeranyltransferase type I.

Authors:  Kimberly T Lane; Lorena S Beese
Journal:  J Lipid Res       Date:  2006-02-13       Impact factor: 5.922

3.  Kinetic mechanism of isoprenylated protein methyltransferase.

Authors:  Y Q Shi; R R Rando
Journal:  J Biol Chem       Date:  1992-05-15       Impact factor: 5.157

4.  Identification of novel peptide substrates for protein farnesyltransferase reveals two substrate classes with distinct sequence selectivities.

Authors:  James L Hougland; Katherine A Hicks; Heather L Hartman; Rebekah A Kelly; Terry J Watt; Carol A Fierke
Journal:  J Mol Biol       Date:  2009-10-28       Impact factor: 5.469

5.  A convenient and genuine equivalent to HZrCp2Cl generated in situ from ZrCp2Cl2-DIBAL-H.

Authors:  Zhihong Huang; Ei-ichi Negishi
Journal:  Org Lett       Date:  2006-08-17       Impact factor: 6.005

6.  Synthesis of Farnesol Analogues through Cu(I)-Mediated Displacements of Allylic THP Ethers by Grignard Reagents.

Authors:  Mark F. Mechelke; David F. Wiemer
Journal:  J Org Chem       Date:  1999-06-25       Impact factor: 4.354

Review 7.  Thematic review series: lipid posttranslational modifications. CAAX modification and membrane targeting of Ras.

Authors:  Latasha P Wright; Mark R Philips
Journal:  J Lipid Res       Date:  2006-03-16       Impact factor: 5.922

Review 8.  Use of synthetic isoprenoid analogues for understanding protein prenyltransferase mechanism and structure.

Authors:  Tamara A Kale; Shih-an J Hsieh; Matt W Rose; Mark D Distefano
Journal:  Curr Top Med Chem       Date:  2003       Impact factor: 3.295

9.  Structure of mammalian protein geranylgeranyltransferase type-I.

Authors:  Jeffrey S Taylor; T Scott Reid; Kimberly L Terry; Patrick J Casey; Lorena S Beese
Journal:  EMBO J       Date:  2003-11-17       Impact factor: 11.598

10.  Farnesyl diphosphate analogues with omega-bioorthogonal azide and alkyne functional groups for protein farnesyl transferase-catalyzed ligation reactions.

Authors:  Guillermo R Labadie; Rajesh Viswanathan; C Dale Poulter
Journal:  J Org Chem       Date:  2007-11-03       Impact factor: 4.354

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  3 in total

1.  Synthesis of Non-natural, Frame-Shifted Isoprenoid Diphosphate Analogues.

Authors:  Kayla J Temple; Elia N Wright; Carol A Fierke; Richard A Gibbs
Journal:  Org Lett       Date:  2016-11-14       Impact factor: 6.005

2.  Bishomoisoprenoid triazole bisphosphonates as inhibitors of geranylgeranyl diphosphate synthase.

Authors:  Veronica S Wills; Joseph I Metzger; Cheryl Allen; Michelle L Varney; David F Wiemer; Sarah A Holstein
Journal:  Bioorg Med Chem       Date:  2017-03-04       Impact factor: 3.641

3.  Amides as bioisosteres of triazole-based geranylgeranyl diphosphate synthase inhibitors.

Authors:  Daniel B Goetz; Michelle L Varney; David F Wiemer; Sarah A Holstein
Journal:  Bioorg Med Chem       Date:  2020-06-30       Impact factor: 3.641

  3 in total

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