Details of Host Protein-DME Interaction (HOSPPI)
General Information of Drug-Metabolizing Enzyme (DME ID: DME0087) | |||||
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DME Name | Aldo-keto reductase 1B1 (AKR1B1), Homo sapiens | DME Info | |||
UniProt ID | |||||
EC Number | EC: 1.1.1.21 (Click to Show/Hide the Complete EC Tree) | ||||
Lineage | Species: Homo sapiens (Click to Show/Hide the Complete Species Lineage) | ||||
Interactome |
Disease Specific Interactions between Host Protein and DME (HOSPPI) | |||||
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ICD Disease Classification 02 Neoplasms | |||||
ICD-11: 2C12 Liver cancer | Click to Show/Hide the Full List of HOSPPI: 1 HOSPPI | ||||
DNA methylation | |||||
DNA methyltransferase (DNMT) | Liver cancer | Moderate hypermethylation | |||
Interaction Name | DNMT-AKR1B1 interaction | ||||
The Methylation Level of Disease Section Compare with the Healthy Individual Tissue | Moderate hypermethylation p-value: 2.63E-03; delta-beta: 2.84E-01 | ||||
Description | DNA methyltransferase (DNMT) is reported to moderatly hyper-methylate the AKR1B1 gene, which leads to a moderatly decreased expression of the drug-metabolizing enzyme Aldo-keto reductase 1B1. As a result, the interaction between DNMT and AKR1B1 can moderatly affect the drug-metabolizing process of Aldo-keto reductase 1B1. | ||||
The Methylation Level of Disease Section Compare with the Adjacent Tissue | Moderate hypermethylation p-value: 1.15E-06; delta-beta: 2.62E-01 | ||||
Description | DNA methyltransferase (DNMT) is reported to moderatly hyper-methylate the AKR1B1 gene, which leads to a moderatly decreased expression of the drug-metabolizing enzyme Aldo-keto reductase 1B1. As a result, the interaction between DNMT and AKR1B1 can moderatly affect the drug-metabolizing process of Aldo-keto reductase 1B1. | ||||
DME methylation in the diseased tissue of patients
DME methylation in the normal tissue adjacent to the diseased tissue of patients
DME methylation in the normal tissue of healthy individuals
DME methylation in tissue other than the diseased tissue of patients
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Violin Diagram of DME Disease-specific Methylation Level | Click to View the Clearer Original Diagram | ||||
ICD-11: 2C82 Prostate cancer | Click to Show/Hide the Full List of HOSPPI: 1 HOSPPI | ||||
DNA methylation | |||||
DNA methyltransferase (DNMT) | Prostate cancer | Moderate hypermethylation | |||
Interaction Name | DNMT-AKR1B1 interaction | ||||
The Methylation Level of Disease Section Compare with the Healthy Individual Tissue | Moderate hypermethylation p-value: 1.04E-73; delta-beta: 2.16E-01 | ||||
Description | DNA methyltransferase (DNMT) is reported to moderatly hyper-methylate the AKR1B1 gene, which leads to a moderatly decreased expression of the drug-metabolizing enzyme Aldo-keto reductase 1B1. As a result, the interaction between DNMT and AKR1B1 can moderatly affect the drug-metabolizing process of Aldo-keto reductase 1B1. | ||||
DME methylation in the diseased tissue of patients
DME methylation in the normal tissue of healthy individuals
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Violin Diagram of DME Disease-specific Methylation Level | Click to View the Clearer Original Diagram | ||||
ICD-11: 2E06 Prostate cancer metastasis | Click to Show/Hide the Full List of HOSPPI: 1 HOSPPI | ||||
DNA methylation | |||||
DNA methyltransferase (DNMT) | Prostate cancer metastasis | Significant hypermethylation | |||
Interaction Name | DNMT-AKR1B1 interaction | ||||
The Methylation Level of Disease Section Compare with the Healthy Individual Tissue | Significant hypermethylation p-value: 2.90E-03; delta-beta: 3.92E-01 | ||||
Description | DNA methyltransferase (DNMT) is reported to significantly hyper-methylate the AKR1B1 gene, which leads to a significantly decreased expression of the drug-metabolizing enzyme Aldo-keto reductase 1B1. As a result, the interaction between DNMT and AKR1B1 can significantly affect the drug-metabolizing process of Aldo-keto reductase 1B1. | ||||
DME methylation in the diseased tissue of patients
DME methylation in the normal tissue of healthy individuals
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Violin Diagram of DME Disease-specific Methylation Level | Click to View the Clearer Original Diagram | ||||
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