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Crystal Structure of the mammalian 20S proteasome at 2.75 A resolution[HYDROLASE]
View in iCn3D Similar StructuresPubMedProteinsConserved DomainsPubChem Compound
Yeast 20S proteasome in complex with PR-957 (epoxide)[HYDROLASE/HYDROLASE INHIBTIOR]
Yeast 20S proteasome in complex with PR-957 (morpholine)[HYDROLASE/HYDROLASE INHIBITOR]
Crystal structure of the yeast 20S proteasome in complex with ligand 2c[hydrolase/hydrolase inhibitor]
View in iCn3D Similar StructuresProteinsConserved DomainsPubChem Compound
Crystal structure of the yeast 20S proteasome in complex with 2b[hydrolase/hydrolase inhibitor]
Crystal structure of yeast 20S proteasome in complex with ligand 2a[hydrolase/hydrolase inhibitor]
Crystal structure of the 20s proteasome from yeast in complex with the proteasome activator PA26 from Trypanosome brucei at 3.2 angstroms resolution[HYDROLASE/HYDROLASE ACTIVATOR]
View in iCn3D Similar StructuresPubMedProteinsConserved Domains
yeast 20S proteasome:glidobactin A-complex[HYDROLASE]
yeast 20S proteasome:syringolin A-complex[HYDROLASE]
CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST IN COMPLEX WITH THE PROTEASOME ACTIVATOR PA26 FROM TRYPANOSOME BRUCEI AT 3.2 ANGSTROMS RESOLUTION[HYDROLASE/HYDROLASE ACTIVATOR]
Structure of yeast 20S open-gate proteasome with Compound 16[HYDROLASE]
Structure of yeast 20S open-gate proteasome with Compound 8[HYDROLASE]
Structure of yeast 20S open-gate proteasome with Compound 6[HYDROLASE]
A GATED CHANNEL INTO THE PROTEASOME CORE PARTICLE[HYDROLASE]
Structure of yeast 20S open-gate proteasome with Compound 25[Hydrolase/Hydrolase Inhibitor]
Structure of yeast 20S open-gate proteasome with Compound 24[Hydrolase/Hydrolase Inhibitor]
Crystal structure of epoxomicin:20s proteasome reveals a molecular basis for selectivity of alpha,beta-epoxyketone proteasome inhibitors[HYDROLASE/HYDROLASE inhibitor]
Proteasome in complex with hydroxyurea derivative HU10[HYDROLASE/HYDROLASE INHIBITOR]
Crystal structure of yeast CP in complex with Belactosin C[HYDROLASE/HYDROLASE INHIBITOR]
Alpha-keto-aldehyde binding mechanism reveals a novel lead structure motif for proteasome inhibition[HYDROLASE/HYDROLASE INHIBITOR]
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