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==Overview==
==Overview==
The hepatitis C virus NS3 protein contains a serine protease domain with a, chymotrypsin-like fold, which is a target for development of therapeutics., We report the crystal structures of this domain complexed with NS4A, cofactor and with two potent, reversible covalent inhibitors spanning the, P1-P4 residues. Both inhibitors bind in an extended backbone conformation, forming an anti-parallel beta-sheet with one enzyme beta-strand. The P1, residue contributes most to the binding energy, whereas P2-P4 side chains, are partially solvent exposed. The structures do not show notable, rearrangements of the active site upon inhibitor binding. These results, are significant for the development of antivirals.
The hepatitis C virus NS3 protein contains a serine protease domain with a chymotrypsin-like fold, which is a target for development of therapeutics. We report the crystal structures of this domain complexed with NS4A cofactor and with two potent, reversible covalent inhibitors spanning the P1-P4 residues. Both inhibitors bind in an extended backbone conformation, forming an anti-parallel beta-sheet with one enzyme beta-strand. The P1 residue contributes most to the binding energy, whereas P2-P4 side chains are partially solvent exposed. The structures do not show notable rearrangements of the active site upon inhibitor binding. These results are significant for the development of antivirals.


==About this Structure==
==About this Structure==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Colarusso, S.]]
[[Category: Colarusso, S.]]
[[Category: Francesco, R.De.]]
[[Category: Francesco, R De.]]
[[Category: Marco, S.Di.]]
[[Category: Marco, S Di.]]
[[Category: Matassa, V.G.]]
[[Category: Matassa, V G.]]
[[Category: Narjes, F.]]
[[Category: Narjes, F.]]
[[Category: Rizzi, M.]]
[[Category: Rizzi, M.]]
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[[Category: serine protease]]
[[Category: serine protease]]


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