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2X9L

Crystal structure of deacetylase-bog complex in biosynthesis pathway of teicoplanin.

Summary for 2X9L
Entry DOI10.2210/pdb2x9l/pdb
Related2XAD 3DFF 3DFK 3DFM
DescriptorN-ACYL GLM PEUDO-TEICOPLANIN DEACETYLASE, ZINC ION, octyl beta-D-glucopyranoside, ... (4 entities in total)
Functional Keywordshydrolase
Biological sourceACTINOPLANES TEICHOMYCETICUS
Total number of polymer chains1
Total formula weight30652.81
Authors
Chan, H.C.,Huang, Y.T.,Lyu, S.Y.,Huang, C.J.,Li, Y.S.,Liu, Y.C.,Chou, C.C.,Tsai, M.D.,Li, T.L. (deposition date: 2010-03-23, release date: 2011-02-09, Last modification date: 2024-11-13)
Primary citationChan, H.C.,Huang, Y.T.,Lyu, S.Y.,Huang, C.J.,Li, Y.S.,Liu, Y.C.,Chou, C.C.,Tsai, M.D.,Li, T.L.
Regioselective Deacetylation Based on Teicoplanin-Complexed Orf2 Crystal Structures.
Mol.Biosyst., 7:1224-, 2011
Cited by
PubMed Abstract: Lipoglycopeptide antibiotics are more effective than vancomycin against MRSA as they carry an extra aliphatic acyl side chain on glucosamine (Glm) at residue 4 (r4). The biosynthesis of the r4 N-acyl Glc moiety at teicoplanin (Tei) or A40926 has been elucidated, in which the primary amine nucleophile of Glm is freed from the r4 GlcNac pseudo-Tei precursor by Orf2* for the subsequent acylation reaction to occur. In this report, two Orf2* structures in complex with β-D-octyl glucoside or Tei were solved. Of the complexed structures, the substrate binding site and a previously unknown hydrophobic cavity were revealed, wherein r4 GlcNac acts as the key signature for molecular recognition and the cavity allows substrates carrying longer acyl side chains in addition to the acetyl group. On the basis of the complexed structures, a triple-mutation mutant S98A/V121A/F193Y is able to regioselectively deacetylate r6 GlcNac pseudo-Tei instead of that at r4. Thereby, novel analogs can be made at the r6 sugar moiety.
PubMed: 21267472
DOI: 10.1039/C0MB00320D
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.732 Å)
Structure validation

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