Literature DB >> 19519368

Red cell glycolytic enzyme disorders caused by mutations: an update.

Fernando Climent1, Feliu Roset, Ada Repiso, Pablo Pérez de la Ossa.   

Abstract

Glycolysis is one of the principle pathways of ATP generation in cells and is present in all cell tissues; in erythrocytes, glycolysis is the only pathway for ATP synthesis since mature red cells lack the internal structures necessary to produce the energy vital for life. Red cell deficiencies have been detected in all erythrocyte glycolytic pathways, although their frequencies differ owing to diverse causes, such as the affected enzyme and severity of clinical manifestations. The number of enzyme deficiencies known is endless. The most frequent glycolysis abnormality is pyruvate kinase deficiency, since around 500 cases are known, the first of which was reported in 1961. However, only approximately 200 cases were due to mutations. In contrast, only one case of phosphoglycerate mutase BB type mutation, described in 2003, has been detected. Most mutations are located in the coding sequences of genes, while others, missense, deletions, insertions, splice defects, premature stop codons and promoter mutations, are also frequent. Understanding of the crystal structure of enzymes permits molecular modelling studies which, in turn, reveal how mutations can affect enzyme structure and function.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19519368     DOI: 10.2174/187152909788488636

Source DB:  PubMed          Journal:  Cardiovasc Hematol Disord Drug Targets        ISSN: 1871-529X


  9 in total

1.  Incomplete and transitory decrease of glycolysis: a new paradigm for anti-angiogenic therapy?

Authors:  Sandra Schoors; Anna Rita Cantelmo; Maria Georgiadou; Peter Stapor; Xingwu Wang; Annelies Quaegebeur; Sandra Cauwenberghs; Brian W Wong; Francesco Bifari; Ilaria Decimo; Luc Schoonjans; Katrien De Bock; Mieke Dewerchin; Peter Carmeliet
Journal:  Cell Cycle       Date:  2013-12-13       Impact factor: 4.534

2.  An infant with chronic hemolytic anemia.

Authors:  Gülen Tüysüz; Gül Nihal Özdemir; Tiraje Celkan
Journal:  Turk Pediatri Ars       Date:  2014-09-01

3.  Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.

Authors:  Prashant Warang; Prabhakar Kedar; Kanjaksha Ghosh; Roshan B Colah
Journal:  Int J Hematol       Date:  2012-07-11       Impact factor: 2.490

4.  Deficiency of nicotinamide mononucleotide adenylyltransferase 3 (nmnat3) causes hemolytic anemia by altering the glycolytic flow in mature erythrocytes.

Authors:  Keisuke Hikosaka; Masashi Ikutani; Masayuki Shito; Kohei Kazuma; Maryam Gulshan; Yoshinori Nagai; Kiyoshi Takatsu; Katsuhiro Konno; Kazuyuki Tobe; Hitoshi Kanno; Takashi Nakagawa
Journal:  J Biol Chem       Date:  2014-04-16       Impact factor: 5.157

5.  SeqHBase: a big data toolset for family based sequencing data analysis.

Authors:  Min He; Thomas N Person; Scott J Hebbring; Ethan Heinzen; Zhan Ye; Steven J Schrodi; Elizabeth W McPherson; Simon M Lin; Peggy L Peissig; Murray H Brilliant; Jason O'Rawe; Reid J Robison; Gholson J Lyon; Kai Wang
Journal:  J Med Genet       Date:  2015-01-13       Impact factor: 6.318

6.  An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation.

Authors:  Gabriela Segerer; Kerstin Hadamek; Matthias Zundler; Agnes Fekete; Annegrit Seifried; Martin J Mueller; Frank Koentgen; Manfred Gessler; Elisabeth Jeanclos; Antje Gohla
Journal:  Sci Rep       Date:  2016-10-12       Impact factor: 4.379

Review 7.  Diagnostic approaches for inherited hemolytic anemia in the genetic era.

Authors:  Yonggoo Kim; Joonhong Park; Myungshin Kim
Journal:  Blood Res       Date:  2017-06-22

8.  Protein Stability, Folding and Misfolding in Human PGK1 Deficiency.

Authors:  Giovanna Valentini; Maristella Maggi; Angel L Pey
Journal:  Biomolecules       Date:  2013-12-18

9.  Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics.

Authors:  Bartholomew P Roland; Alison M Zeccola; Samantha B Larsen; Christopher G Amrich; Aaron D Talsma; Kimberly A Stuchul; Annie Heroux; Edwin S Levitan; Andrew P VanDemark; Michael J Palladino
Journal:  PLoS Genet       Date:  2016-03-31       Impact factor: 5.917

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.