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2UZF

Crystal structure of Staphylococcus aureus 1,4-dihydroxy-2-naphthoyl CoA synthase (MenB) in complex with acetoacetyl CoA

Summary for 2UZF
Entry DOI10.2210/pdb2uzf/pdb
DescriptorNAPHTHOATE SYNTHASE, ACETOACETYL-COENZYME A (3 entities in total)
Functional Keywordslyase, menaquinone biosynthesis
Biological sourceSTAPHYLOCOCCUS AUREUS
Total number of polymer chains2
Total formula weight61776.77
Authors
Ulaganathan, V.,Buetow, L.,Hunter, W.N. (deposition date: 2007-04-27, release date: 2007-11-13, Last modification date: 2023-12-13)
Primary citationUlaganathan, V.,Agacan, M.F.,Buetow, L.,Tulloch, L.B.,Hunter, W.N.
Structure of Staphylococcus Aureus1,4-Dihydroxy-2-Naphthoyl-Coa Synthase (Menb) in Complex with Acetoacetyl-Coa.
Acta Crystallogr.,Sect.F, 63:908-, 2007
Cited by
PubMed Abstract: Vitamin K(2), or menaquinone, is an essential cofactor for many organisms and the enzymes involved in its biosynthesis are potential antimicrobial drug targets. One of these enzymes, 1,4-dihydroxy-2-naphthoyl-CoA synthase (MenB) from the pathogen Staphylococcus aureus, has been obtained in recombinant form and its quaternary structure has been analyzed in solution. Cubic crystals of the enzyme allowed a low-resolution structure (2.9 A) to be determined. The asymmetric unit consists of two subunits and a crystallographic threefold axis of symmetry generates a hexamer consistent with size-exclusion chromatography. Analytical ultracentrifugation indicates the presence of six states in solution, monomeric through to hexameric, with the dimer noted as being particularly stable. MenB displays the crotonase-family fold with distinct N- and C-terminal domains and a flexible segment of structure around the active site. The smaller C-terminal domain plays an important role in oligomerization and also in substrate binding. The presence of acetoacetyl-CoA in one of the two active sites present in the asymmetric unit indicates how part of the substrate binds and facilitates comparisons with the structure of Mycobacterium tuberculosis MenB.
PubMed: 18007038
DOI: 10.1107/S1744309107047720
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.9 Å)
Structure validation

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