Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-(+)-Cysteine | HCID 5862 | — |
| Reactant | 5'-Atp | HCID 5957 | — |
| Reactant | D-1,4-Dithiothreitol | HCID 446094 | — |
| Reactant | HCID 46878468 | HCID 46878468 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Solvent | HCID 46878469 | HCID 46878469 | — |
| Product | N-Acetyl-L-Cysteine | HCID 12035 | — |
Reaction Steps
Incubation of 100 μM Cys and 50 μM GlcN-Ins with 1 mM ATP in phosphate buffer, pH 7.5, containing 1 DTT after addition of cell extract supernatant resulted in an increase in Cys-GlcN-Ins from <0.2 to 26 μM over 60 min while the MSH content declined from 15 to 13 μM, corresponding to the MSH content present in the undialyzed cell extract. A parallel experiment with 100 μM AcCys in place of Cys resulted in an increase from <0.2 to 20 μM Cys-GlcN-Ins, and no change in MSH content (15 μM); however, marked conversion of AcCys to Cys had occurred by 60 min ([Cys]/[AcCys]˜3). If the MSH had increased by as much as 2 μM (10% of the change in Cys-GlcN-Ins) the change would have been detected and this experiment therefore established that conversion of Cys to Cys-GlcN-Ins is at least an order of magnitude faster than conversion of AcCys to MSH under these conditions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06780418B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-6b162d157f7f4cd49d4eb75183358910 |
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| Source note | uspto-grants-2004_08 |
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