2og6: Difference between revisions
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{{STRUCTURE_2og6| PDB=2og6 | SCENE= }} | |||
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'''Crystal structure of asparagine oxygenase in complex with Fe(II)''' | '''Crystal structure of asparagine oxygenase in complex with Fe(II)''' | ||
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[[Category: Essen, L O.]] | [[Category: Essen, L O.]] | ||
[[Category: Strieker, M.]] | [[Category: Strieker, M.]] | ||
[[Category: | [[Category: Alpha-ketoglutarate oxygenase]] | ||
[[Category: | [[Category: Beta-hydroxylated amino acid]] | ||
[[Category: | [[Category: Nonribosomal peptide synthesis]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 10:50:31 2008'' | |||
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Revision as of 07:50, 4 May 2008
Crystal structure of asparagine oxygenase in complex with Fe(II)
Overview
Non-ribosomally synthesized lipopeptide antibiotics of the daptomycin type are known to contain unnatural beta-modified amino acids, which are essential for bioactivity. Here we present the biochemical and structural basis for the incorporation of 3-hydroxyasparagine at position 9 in the 11-residue acidic lipopeptide lactone calcium-dependent antibiotic (CDA). Direct hydroxylation of l-asparagine by AsnO, a non-heme Fe(2+)/alpha-ketoglutarate-dependent oxygenase encoded by the CDA biosynthesis gene cluster, was validated by Fmoc derivatization of the reaction product and LC/MS analysis. The 1.45, 1.92, and 1.66 A crystal structures of AsnO as apoprotein, Fe(2+) complex, and product complex, respectively, with (2S,3S)-3-hydroxyasparagine and succinate revealed the stereoselectivity and substrate specificity of AsnO. The comparison of native and product-complex structures of AsnO showed a lid-like region (residues F208-E223) that seals the active site upon substrate binding and shields it from sterically demanding peptide substrates. Accordingly, beta-hydroxylated asparagine is synthesized prior to its incorporation into the growing CDA peptide. The AsnO structure could serve as a template for engineering novel enzymes for the synthesis of beta-hydroxylated amino acids.
About this Structure
2OG6 is a Single protein structure of sequence from Bacteria. Full crystallographic information is available from OCA.
Reference
Mechanistic and structural basis of stereospecific Cbeta-hydroxylation in calcium-dependent antibiotic, a daptomycin-type lipopeptide., Strieker M, Kopp F, Mahlert C, Essen LO, Marahiel MA, ACS Chem Biol. 2007 Mar 20;2(3):187-96. PMID:17373765 Page seeded by OCA on Sun May 4 10:50:31 2008
