Disease Specific Interactions between Host Protein and DME (HOSPPI) |
Drug co-metabolism |
Cometabolized drug: Riboflavin |
Click to Show/Hide the Full List of HOSPPI: 7 HOSPPI
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Acid phosphatase-like protein 1 (ACP6) |
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DME ID |
DME0231
DME Info
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Uniprot ID |
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Interaction Name |
ACP6-nfrA1 interaction |
[1], [2] |
Description |
The interaction, between human Acid phosphatase-like protein 1 and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Cytochrome P450 1A1 (CYP1A1) |
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DME ID |
DME0006
DME Info
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Uniprot ID |
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Interaction Name |
CYP1A1-nfrA1 interaction |
[1], [3] |
Description |
The interaction, between human Cytochrome P450 1A1 and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Eosinophil peroxidase (EPX) |
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DME ID |
DME0244
DME Info
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Uniprot ID |
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Interaction Name |
EPX-nfrA1 interaction |
[1], [2] |
Description |
The interaction, between human Eosinophil peroxidase and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Prostatic acid phosphatase (ACP3) |
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DME ID |
DME0232
DME Info
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Uniprot ID |
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Interaction Name |
ACP3-nfrA1 interaction |
[1], [2] |
Description |
The interaction, between human Prostatic acid phosphatase and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Tartrate-resistant acid ATPase (ACP5) |
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DME ID |
DME0230
DME Info
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Uniprot ID |
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Interaction Name |
ACP5-nfrA1 interaction |
[1], [2] |
Description |
The interaction, between human Tartrate-resistant acid ATPase and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Testicular acid phosphatase (ACP4) |
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DME ID |
DME0229
DME Info
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Uniprot ID |
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Interaction Name |
ACP4-nfrA1 interaction |
[1], [2] |
Description |
The interaction, between human Testicular acid phosphatase and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Xylosyl phosphatase (PXYLP1) |
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DME ID |
DME0250
DME Info
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Uniprot ID |
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Interaction Name |
PXYLP1-nfrA1 interaction |
[1], [2] |
Description |
The interaction, between human Xylosyl phosphatase and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Riboflavin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Cometabolized drug: Nitrofural |
Click to Show/Hide the Full List of HOSPPI: 1 HOSPPI
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Cytochrome P450 2D6 (CYP2D6) |
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DME ID |
DME0009
DME Info
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Uniprot ID |
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Interaction Name |
CYP2D6-nfrA1 interaction |
[1], [4], [5] |
Description |
The interaction, between human Cytochrome P450 2D6 and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Nitrofural, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
Cometabolized drug: Nitrofurantoin |
Click to Show/Hide the Full List of HOSPPI: 1 HOSPPI
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NADPH-cytochrome P450 reductase (CPR) |
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DME ID |
DME0076
DME Info
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Uniprot ID |
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Interaction Name |
CPR-nfrA1 interaction |
[1], [4], [6] |
Description |
The interaction, between human NADPH-cytochrome P450 reductase and NADPH-dependent nitroreductase from Bacillus subtilis which collectively metabolize the drug Nitrofurantoin, is reported to affect the efficacy, safety or bioavailability of this drug via interfering with it metabolism. |
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