HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249950Generated: October 30, 2026
L-(+)-Cysteine → (2R)-2-Acetamido-3-({(2R,3S,4R)-3-hydroxy-2-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-5-oxopyrrolidine-2-carbonyl}sulfanyl)propanoic acidLactacystin
https://huagongshe.com/reaction/1249950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-(+)-Cysteine | HCID 5862 | — |
| Reactant | L-Methionine | HCID 6137 | — |
| Reactant | MG132 | HCID 462382 | — |
| Reactant | HCID 88195029 | HCID 88195029 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (2R)-2-Acetamido-3-({(2R,3S,4R)-3-hydroxy-2-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-5-oxopyrrolidine-2-carbonyl}sulfanyl)propanoic acidLactacystin | HCID 6610292 | — |
Reaction Steps
COS cells were plated onto 100 mm dishes, then, with DEAE-Destran, either mock transfected, or transfected with 3 μg of pcDNA plasmid containing the human p105 cDNA. Forty-eight hrs after transfection, cells were pretreated for 1 hour with 0.5% DMSO, 50 μM calpain inhibitor II, 50 μM MG132, or 10 μM β-lactone. Cells were then pulse labelled with 250 uCi/plate of 35S-methionine/cysteine for 15 minutes, and either harvested immediately or followed by a 2 hour chase with excess unlabelled methionine and cysteine. Cells were then lysed with SDS/Tris, and proteins were immunoprecipitated with anti-p50 antibodies (recognize the N-terminal half of the p105 protein). These proteins were then separated on a 10% SDS-polyacrylamide gel, which was then fixed, dried, and exposed to autoradiographic film.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06335358B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-124c243e3ae64adb81a7877faf9d4fab |
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| Source note | uspto-grants-2002_01 |
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