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Updated: Jul 11, 2026

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
Published on: November 29, 2014
Structure determination of the O-methyltransferase NovP using the 'free lunch algorithm' as implemented in SHELXE
Isabel Usón1, Clare E M Stevenson, David M Lawson
1Institució Catalana de Recerca i Estudis Avançats at Instituto de Biología Molecular de Barcelona (IBMB-CSIC), Jordi Girona 18-26, 08034 Barcelona, Spain. uson@ibmb.csic.es
Abstract:
NovP is an S-adenosyl-L-methionine-dependent O-methyltransferase from Streptomyces spheroides (subunit MW = 29 967 Da). Recombinant N-terminally His-tagged NovP crystallizes in space group P2, with approximate unit-cell parameters a = 51.81, b = 46.04, c = 61.22 A, beta = 105.0 degrees , giving a solvent content of 44% for a single copy of the His-tagged protomer per asymmetric unit. Native synchrotron data to a resolution of 1.35 A were combined with three other native data sets collected at lower resolution (both in-house and at the synchrotron) for the sake of completeness and better scaling. Data to 2.45 A resolution were subsequently recorded in-house from a single mercury derivative. Three partial mercury sites could be located with SHELXD, but the resulting phases had a mean error of about 81 degrees and in our hands did not yield an interpretable map using standard automated software. Nevertheless, the structure of NovP could be solved by first tracing a small part of the structure by hand and then extrapolating within and beyond the experimental resolution limit using the ;free lunch algorithm' in SHELXE. The resulting phases have a mean phase error of 17 degrees relative to a refined model.
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