Evidence map›Paper›PMID 36381187›Full record

ArticleBioMedicine2022

Preliminary Study of Structural Changes of Glucose-6-Phosphate Dehydrogenase Deficiency Variants.

Naveen E Louis, Muaawia A Hamza, Puteri Nsd Engku Baharuddin Baharuddin, Shamini Chandran, Nurriza A Latif, Mona A Alonazi, Khairul B A Halim, Arjumand Warsy, Syazwani I Amran

Abstract read
In one paragraph

Article in BioMedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Naveen E LouisDepartment of Biosciences, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysia.
Muaawia A HamzaFaculty of Medicine, King Fahad Medical City, Riyadh, Kingdom of Saudi Arabia.
Puteri Nsd Engku Baharuddin BaharuddinDepartment of Biosciences, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysia.
Shamini ChandranDepartment of Biosciences, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysia.
Nurriza A LatifDepartment of Biosciences, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysia.
Mona A AlonaziDepartment of Biochemistry, Science College, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Khairul B A HalimDepartment of Biotechnology, Kulliyyah of Science, International Islamic University Malaysia, 25200, Bandar Indera Mahkota Kuantan, Pahang, Malaysia.
Arjumand WarsyCentral Laboratory, Center Female Center for Scientific and Medical Studies, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Syazwani I AmranDepartment of Biosciences, Faculty of Science, Universiti Teknologi Malaysia, Johor Bahru, Johor, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency disorder affecting over 400 million individuals worldwide. G6PD protects red blood cells (RBC) from the harmful effects of oxidative substances. There are more than 400 G6PD mutations, of which 186 variants have shown to be linked to G6PD deficiency by decreasing the activity or stability of the enzyme. Different variants manifest different clinical phenotypes which complicate comprehending the mechanism of the disease. In order to carry out computational approaches to elucidate the structural changes of different G6PD variants that are common to the Asian population, a complete G6PD monomer-ligand complex was constructed using AutoDock 4.2, and the molecular dynamics simulation package GROMACS 4.6.7 was used to study the protein dynamics. The G410D and V291M variants were chosen to represent classes I and II respectively and were created by

Indexed as

G6PD deficiencyMolecular dynamics simulationProtein-ligand complex

Identifiers

PMID36381187
PMCPMC9629405

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.