Literature DB >> 3493920

The only inositol tetrakisphosphate detectable in avian erythrocytes is the isomer lacking phosphate at position 3: a NMR study.

G W Mayr, W Dietrich.   

Abstract

Avian red blood cells contain a millimolar amount of inositol polyphosphate which plays a role as an allosteric effector of hemoglobin. We confirmed the structure of this substance by NMR techniques as purely myo-inositol 1,3,4,5,6-pentakisphosphate. Based on present knowledge this effector is synthesized from inositol trisphosphate by successive phosphorylation. In a search for biosynthetic and degradative intermediates of inositol pentakisphosphate we found only one inositol tetrakisphosphate isomer. Its structure was unambiguously assigned by proton, 13C- and 31P-NMR to myo-inositol 1,4,5,6-tetrakisphosphate. As in mammalian cells the major inositol tetrakisphosphate isomer is myo-inositol 1,3,4,5-tetrakisphosphate, there seem to be differences between avian red blood cells and mammalian cells in the routes of inositol polyphosphate formation and/or degradation.

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Year:  1987        PMID: 3493920     DOI: 10.1016/0014-5793(87)81505-3

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  8 in total

1.  A high-affinity inositol 1,3,4,5-tetrakisphosphate receptor protein from brain is specifically labelled by a newly synthesized photoaffinity analogue, N-(4-azidosalicyl)aminoethanol(1)-1-phospho-D-myo-inositol 3,4,5-trisphosphate.

Authors:  G Reiser; R Schäfer; F Donié; E Hülser; M Nehls-Sahabandu; G W Mayr
Journal:  Biochem J       Date:  1991-12-01       Impact factor: 3.857

2.  Asymmetric phosphorylation through catalytic P(III) phosphoramidite transfer: enantioselective synthesis of D-myo-inositol-6-phosphate.

Authors:  Peter A Jordan; Katherine J Kayser-Bricker; Scott J Miller
Journal:  Proc Natl Acad Sci U S A       Date:  2010-05-03       Impact factor: 11.205

3.  A novel metal-dye detection system permits picomolar-range h.p.l.c. analysis of inositol polyphosphates from non-radioactively labelled cell or tissue specimens.

Authors:  G W Mayr
Journal:  Biochem J       Date:  1988-09-01       Impact factor: 3.857

4.  L-myo-inositol 1,4,5,6-tetrakisphosphate is present in both mammalian and avian cells.

Authors:  L Stephens; P T Hawkins; N Carter; S B Chahwala; A J Morris; A D Whetton; P C Downes
Journal:  Biochem J       Date:  1988-01-01       Impact factor: 3.857

5.  The quantitative spectrum of inositol phosphate metabolites in avian erythrocytes, analysed by proton n.m.r. and h.p.l.c. with direct isomer detection.

Authors:  T Radenberg; P Scholz; G Bergmann; G W Mayr
Journal:  Biochem J       Date:  1989-12-01       Impact factor: 3.857

6.  Inositol 1,4-bisphosphate is an allosteric activator of muscle-type 6-phosphofructo-1-kinase.

Authors:  G W Mayr
Journal:  Biochem J       Date:  1989-04-15       Impact factor: 3.857

7.  Catalyst-Dependent Syntheses of Phosphatidylinositol-5 Phosphate-DiC8 and its Enantiomer.

Authors:  Katherine J Kayser-Bricker; Peter A Jordan; Scott J Miller
Journal:  Tetrahedron       Date:  2008-07-14       Impact factor: 2.457

8.  myo-inositol pentakisphosphates. Structure, biological occurrence and phosphorylation to myo-inositol hexakisphosphate.

Authors:  L R Stephens; P T Hawkins; A F Stanley; T Moore; D R Poyner; P J Morris; M R Hanley; R R Kay; R F Irvine
Journal:  Biochem J       Date:  1991-04-15       Impact factor: 3.857

  8 in total

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