Crystal packing of Bmlp6.

<p>The asymmetric unit of Bmlp6 (shown with unit cell outline) is composed of five protein molecules, A–E, represented by different colors.</p

Electron density maps of Bmlp6.

<p>(A, B) <i>Fo-Fc</i> and <i>2Fo-Fc</i> electron density maps (contour 5.0 σ and 1.0 σ, respectively), unequivocally demonstrate that residue 217 of Bmlp6 (green) is not Tyr but Asn. (C) <i>2Fo-Fc</i> electron density map (contour 1.0 σ) of a loop (residues 161–170) containing disulfide bridge is presented to illustrate that electron density maps were of a very good quality also at the loop regions. For both fragments the molecule A was arbitrary chosen.</p

Potential binding sites of the Bmlp6 protein.

<p>Potential binding sites of the Bmlp6 protein.</p

Electrostatic surface potential of Bmlp6, Bmlp7 and Bmlp3 at pH 6.5.

<p>Electrostatic surface potential of Bmlp6, Bmlp7 and Bmlp3 was calculated using the <i>APBS</i> algorithm <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0108761#pone.0108761-Baker1" target="_blank">[52]</a> and the <i>PDB2PQR</i> program <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0108761#pone.0108761-Dolinsky1" target="_blank">[53]</a>, <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0108761#pone.0108761-Dolinsky2" target="_blank">[54]</a> at pH 6.5, which is the physiological pH of silkworm hemolymph. The protein surfaces are shown in the same orientation, in two different views for each protein. The positive and negative charges are colored blue and red, respectively, according to the scale. The <i>APBS</i> writes out the electrostatic potential in dimensionless units of k_bTe_c⁻¹ where k_b is Boltzmann's constant, T is the temperature of calculation and e_c is the charge of an electron <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0108761#pone.0108761-Baker1" target="_blank">[52]</a>.</p

Potential binding sites of Bmlp3 and Bmlp6.

<p>Potential binding sites of Bmlp3 (blue/pink) and of Bmlp6 (green/yellow) were marked as No. 1–4 and Po.1–2, respectively. Two different views of Bmlp6 are shown to present both cavities.</p

Alignment of sequences corresponding to Bmlp6.

<p>Amino acid sequence alignment of Bmlp6 (UniProt: A7LIK7; NCBI-Protein: NP_001095198), PBMHPC-23 (UniProt: P09338), PBMHPC-12 (UniPtot: P09335) and Bmlp6_SilkDB (SilkDB: BGIBMGA004457) calculated in ClustalW (<a href="http://www.ebi.ac.uk/Tools/msa/clustalw2/" target="_blank">http://www.ebi.ac.uk/Tools/msa/clustalw2/</a>). The alignment is colored according to identity (dark blue) and similarity (light blue) using Jalview (<a href="http://www.jalview.org/" target="_blank">http://www.jalview.org/</a>) <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0108761#pone.0108761-Waterhouse1" target="_blank">[60]</a>. The evident sequencing error at the C-terminus of Bmlp6_SilkDB (highlighted in dark red, starting from position 194) has been disregarded in sequence similarity calculations. The only discrepancy between Bmlp6 (UniProt: A7LIK7) and the amino acid sequence determined by X-ray crystallography is indicated by white font, at position 217. The N-terminal sequence of Bmlp6 established by Edman degradation is boxed. The displayed sequences correspond to mature proteins without signal peptides.</p

Diffraction data collection and refinement statistics.

a<p>Values in parentheses are for the highest resolution shell.</p>b<p><i>R_merge</i> =  ∑_h∑_j | I_hj - h> |/∑_h∑_j I_hj, where I_hj is the intensity of observation j of reflection h.</p>c<p><i>R_work</i> =  ∑_h | | F_o| - | F_c| |/∑_h | F_o| for all reflections, where F_o and F_c are observed and calculated structure factors, respectively. <i>R_free</i> is calculated analogously for the test reflections, randomly selected and excluded from the refinement.</p><p>Diffraction data collection and refinement statistics.</p