Gene Details: GPI


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General Information

Gene Name: GPI (Glucose-6-phosphate isomerase)
Synonym:
Short Names: GPI;
Alternative Names: Autocrine motility factor;Neuroleukin;Phosphoglucose isomerase;Phosphohexose isomerase;Sperm antigen 36;

Notes:


Description from Dr.Glyco-GPT:

Write a 100-350 word essay about the enzyme human GPI. Provide information related to enzyme: i) function, ii) reaction pathways, ii) Location, and iv) diseases. In writing include these four subheadings

### Function
Human GPI, or glucose-6-phosphate isomerase, is a multifunctional enzyme that plays a crucial role in both glycolysis and gluconeogenesis. GPI catalyzes the reversible isomerization of glucose-6-phosphate to fructose-6-phosphate, a critical step in glycolysis for energy production and in gluconeogenesis for glucose synthesis. Additionally, GPI has roles outside of metabolism, functioning as a cytokine (neuroleukin), a growth factor (autocrine motility factor), and a lymphokine, influencing various biological processes, including cell motility and immune response.

### Reaction Pathways
GPI functions primarily within the glycolysis pathway, where it converts glucose-6-phosphate into fructose-6-phosphate, facilitating the continuation of glycolysis to produce energy in the form of ATP. In gluconeogenesis, the enzyme operates in reverse, contributing to glucose production from non-carbohydrate precursors. Beyond its metabolic roles, GPI is involved in signaling pathways where it acts as a cytokine or growth factor, influencing cell proliferation, differentiation, and migration.

### Location
GPI is predominantly located in the cytoplasm, where it carries out its metabolic functions in glycolysis and gluconeogenesis. However, GPI can also be secreted extracellularly, where it acts as a cytokine or growth factor, influencing immune responses and cell motility. The enzyme’s ability to function in multiple cellular compartments underscores its importance in both metabolic processes and cell signaling.

### Diseases
Mutations in the GPI gene are associated with a rare genetic disorder known as GPI deficiency, which can lead to a form of hereditary nonspherocytic hemolytic anemia. This condition is characterized by chronic hemolysis due to the inability of red blood cells to generate sufficient energy, as GPI deficiency impairs glycolysis. Patients with GPI deficiency may also experience neurological symptoms, such as intellectual disability and motor dysfunction, due to the enzyme’s role in neural cells. Additionally, abnormal GPI activity has been implicated in cancer, where its role as a growth factor can promote tumor progression and metastasis. Understanding the diverse functions of GPI is crucial for diagnosing and developing treatments for these conditions.

Catalytic Activity

Reaction Image

Reaction and Disease Links

EC # (IUBMB): 5.3.1.9
Brenda: 5.3.1.9
OMIM: 172400 613470
KEGG: 2821
Rhea: 11816
Reactome : R-HSA-5628897 R-HSA-6798695 R-HSA-70171 R-HSA-70263

Transcript levels (Cell lines and Single cell data) URL


CRISPR-knockout

CRISPR-activation

CRISPR-inactivation


Top 10 TFs

TF Score
HNRNPK 1.685818
SON 1.655635
RBM39 1.642061
PCBP1 1.623585
XRCC5 1.617330
TCF25 1.616342
SRSF3 1.613420
SUMO2 1.604995
PCBP2 1.589988
SFPQ 1.570208


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