Erratum: Rv0100, a proposed acyl carrier protein in Mycobacterium tuberculosis: Expression, purification and crystallization (Acta Crystallographica Section F: Structural Biology Communications (2019) F75 (646-651) DOI: 10.1107/S2053230X19012652)

As described in the article by Bondoc et al. (2019), attempts to solve the crystal structure (2 monomers per a.u. in the H3 cell), using existing structural homologs of Rv0100 Mycobacterium tuberculosis from the Protein Data Bank failed. Structural models obtained from the amino-acid sequence using the I-THASSER protein prediction server also failed. Refinement of tentative solutions obtained by MOLREP and PHASER stalled at Rw = 0.44, Rf = 0.51, even when assuming a lower symmetry P1 lattice with nearly H3 pseudo-symmetry. Detailed examination of the PDB entries related to proteins from Mycobacterium smegmatis, the organism that was used as an expression strain, revealed the existence of entry 3gwm corresponding to the crystal structure of the holo-[acyl-carrierprotein] synthase (ACPS). This structure was released in 2010 (Poulsen, C., Wilmanns, M. & Song, Y. H., unpublished work). The crystallographic parameters for this deposition (space group H3, a = 67.45, b = 67.45, c = 86.06 Å , α = β = 90, γ = 120°) strongly suggested that it was the same protein as the one we had crystallized. Using the protein structure from entry 3gwm, a molecular replacement solution was readily found and was further refined to Rw = 0.19, Rf = 0.25 following standard protocols using the previously reported crystallographic data to 2.0 Å resolution. The amino-acid sequence of the refined protein was fully consistent with the sequence in the ACPS entry, and significant structural differences were found only in the proximity of the three SO4 anions bound in 3gwm but not in the serendipitously found structure, since there was no sulfate in our crystallization media. The r.m.s.d. between 128 ISSN 2053-230X equivalent Cα carbons in the two structures was 0.58 Å (mean deviation 0.33 Å ). We hypothesize that our expression in the M. smegmatis strain resulted in the co-purification of ACPS protein from M. smegmatis, as a minor contaminant. This is consistent with the fact that only two very small (10-20 mm) crystals were observed in the crystallization droplet and it took about nine months for these crystals to appear. We are certain that the predominant purified protein is Rv0100 from M. tuberculosis confirmed through both mass spectrometry and the fact that the histidine tag was used to isolate the protein. We are confident that the ACPS protein (MW ' 14 000 Da) was a minor contaminant that co-purified alongside Rv0100 whose molecular weight is significantly different (11 122 Da).