Evidence mapPaperPMID 41537922Full record

ReviewThe protein journal2026

Structure, Mutation, Functional Domain Roles and Medical Implications of Glycerol Kinase.

Emmanuel Oluwadare Balogun, Israel Ogwuche Ogra, Uche Samuel Ndidi, Daniel Thakuma Tizhe, Okechukwu Kalu Iroha, Godwin Unekwuojo Ebiloma, Ghulam Jeelani, Tomoyoshi Nozaki, Jair Siqueira-Neto, Harry P De Koning and 1 more

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In one paragraph

Review in The protein journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Emmanuel Oluwadare BalogunDepartment of Biochemistry, Ahmadu Bello University, Zaria, Kaduna State, Nigeria.
Israel Ogwuche OgraDepartment of Biochemistry, Ahmadu Bello University, Zaria, Kaduna State, Nigeria.
Uche Samuel NdidiDepartment of Biochemistry, Ahmadu Bello University, Zaria, Kaduna State, Nigeria. usndidi@abu.edu.ng.
Daniel Thakuma TizheAdamawa State Post Primary Schools Management Board, P.M.B. 2260, Yola, 640230, Nigeria.
Okechukwu Kalu IrohaUNESCO International Centre for Biotechnology, Nsukka, 410001, Enugu State, Nigeria.
Godwin Unekwuojo EbilomaSchool of Science, Engineering and Environment, University of Salford, Manchester, M5 4NT, UK.
Ghulam JeelaniDepartment of Biomedical Chemistry, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Tomoyoshi NozakiDepartment of Biomedical Chemistry, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Jair Siqueira-NetoCenter for Discovery and Innovation in Parasitic Diseases, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, USA.
Harry P De KoningSchool of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G43 2DX, UK.
Tomoo ShibaGraduate School of Science and Technology, Kyoto Institute of Technology, Sakyo, Kyoto, 606-8585, Japan.

Funding

Tertiary Education Trust Fund TETF/DR&D/UNI/ZARIA/IBR/2024/BATCH 8/02
6 · The paper itself

Abstract

Glycerol kinase (GK) is a key part of glycerol metabolism. It connects the metabolic pathways for lipids and carbohydrates by phosphorylating glycerol to glycerol-3-phosphate in an ATP-dependent reaction. This is essential for maintaining carbohydrate homeostasis, plasma glycerol withdrawal, and the utilization of glycerol by different tissues. Together, these processes impact glucose uptake and lipid metabolism. This review discusses the structure of GK, highlights the implications of mutations in the primary sequence, and provides insights on the roles of the various functional domains in the GK-catalyzed reaction. It also discussed the roles of GK in glycerol metabolism, energy production, and its connections with various cellular pathways and disease conditions. The proper regulation of GK activity is crucial, reflecting its critical role in various important cellular processes. Therefore, its regulation has been analyzed from the gene level to posttranslational modification and has implications for GK-linked disease. Separately, the critical role of this enzyme in some disease-causing organisms made it a promising target for inhibitor development. We here explore the current state of GK inhibitor research and discuss strategies for their development. Challenges in GK inhibitor research are identified, and approaches such as high-throughput screening, structure-based drug design, and computational modelling for discovering novel inhibitors are reviewed. Finally, the review highlights critical areas for further research, including the role of GK in synthetic biology and tumour development, among others.

Indexed as

Enzyme InhibitorsGlycerol KinaseMutationAnimalsGlycerolHumansLipid MetabolismModels, MolecularProtein DomainsEnzyme InhibitorsGlycerolGlycerol KinaseEnzyme functionEnzyme regulationGlycerol kinaseGlycerol metabolismInhibitor developmentLipid metabolismStructure-based inhibitor design

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.