2f16
From Proteopedia
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[[Category: Beta-sandwich flanked by helice]] | [[Category: Beta-sandwich flanked by helice]] | ||
[[Category: Complex structure covalently bound to the synthetic inihibtor bortezomib]] | [[Category: Complex structure covalently bound to the synthetic inihibtor bortezomib]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | [[Category: Hydrolase]] |
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Jun 5 10:00:52 2008'' | ||
Revision as of 07:00, 5 June 2008
Crystal structure of the yeast 20S proteasome in complex with bortezomib
Overview
The dipeptide boronic acid bortezomib, also termed VELCADE, is a proteasome inhibitor now in use for the treatment of multiple myeloma, and its use for the treatment of other malignancies is being explored. We determined the crystal structure of the yeast 20S proteasome in complex with bortezomib to establish the specificity and binding mode of bortezomib to the proteasome's different catalytically active sites. This structure should enable the rational design of new boronic acid derivatives with improved affinities and specificities for individual active subunits.
About this Structure
2F16 is a Protein complex structure of sequences from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.
Reference
Crystal structure of the boronic acid-based proteasome inhibitor bortezomib in complex with the yeast 20S proteasome., Groll M, Berkers CR, Ploegh HL, Ovaa H, Structure. 2006 Mar;14(3):451-6. PMID:16531229 Page seeded by OCA on Thu Jun 5 10:00:52 2008
