TY - JOUR
T1 - Structural organization of WrbA in apo- and holoprotein crystals
AU - Wolfova, Julie
AU - Smatanova, Ivana Kuta
AU - Brynda, Jiri
AU - Mesters, Jeroen R.
AU - Lapkouski, Mikalai
AU - Kuty, Michal
AU - Natalello, Antonino
AU - Chatterjee, Neal
AU - Chern, Sy Yeu
AU - Ebbel, Erin
AU - Ricci, Angela
AU - Grandori, Rita
AU - Ettrich, Rüdiger
AU - Carey, Jannette
N1 - Funding Information:
Catherine Lawson contributed valuable comments during the preparation of the manuscript. This research was supported by the U.S. National Science Foundation ( INT03-09049 to J.C.) and the Ministry of Education of the Czech Republic ( Kontakt ME09016, LC06010 and MSM6007665808 ) and by the Academy of Sciences of the Czech Republic ( AV0Z60870520 ). We thank the EMBL for access to the X12 beamline of DESY in Hamburg.
PY - 2009/9
Y1 - 2009/9
N2 - Two previously reported holoprotein crystal forms of the flavodoxin-like E. coli protein WrbA, diffracting to 2.6 and 2.0 Å resolution, and new crystals of WrbA apoprotein diffracting to 1.85 Å, are refined and analysed comparatively through the lens of flavodoxin structures. The results indicate that differences between apo- and holoWrbA crystal structures are manifested on many levels of protein organization as well as in the FMN-binding sites. Evaluation of the influence of crystal contacts by comparison of lattice packing reveals the protein's global response to FMN binding. Structural changes upon cofactor binding are compared with the monomeric flavodoxins. Topologically non-equivalent residues undergo remarkably similar local structural changes upon FMN binding to WrbA or to flavodoxin, despite differences in multimeric organization and residue types at the binding sites. Analysis of the three crystal structures described here, together with flavodoxin structures, rationalizes functional similarities and differences of the WrbAs relative to flavodoxins, leading to a new understanding of the defining features of WrbAs. The results suggest that WrbAs are not a remote and unusual branch of the flavodoxin family as previously thought but rather a central member with unifying structural features.
AB - Two previously reported holoprotein crystal forms of the flavodoxin-like E. coli protein WrbA, diffracting to 2.6 and 2.0 Å resolution, and new crystals of WrbA apoprotein diffracting to 1.85 Å, are refined and analysed comparatively through the lens of flavodoxin structures. The results indicate that differences between apo- and holoWrbA crystal structures are manifested on many levels of protein organization as well as in the FMN-binding sites. Evaluation of the influence of crystal contacts by comparison of lattice packing reveals the protein's global response to FMN binding. Structural changes upon cofactor binding are compared with the monomeric flavodoxins. Topologically non-equivalent residues undergo remarkably similar local structural changes upon FMN binding to WrbA or to flavodoxin, despite differences in multimeric organization and residue types at the binding sites. Analysis of the three crystal structures described here, together with flavodoxin structures, rationalizes functional similarities and differences of the WrbAs relative to flavodoxins, leading to a new understanding of the defining features of WrbAs. The results suggest that WrbAs are not a remote and unusual branch of the flavodoxin family as previously thought but rather a central member with unifying structural features.
KW - Diffraction resolution
KW - Dimerization
KW - Disulfide
KW - Electrostatic potential surface
KW - NAD(P)H:quinone oxidoreductase
KW - Trichloroacetic acid
KW - Twisted open-sheet fold
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U2 - 10.1016/j.bbapap.2009.08.001
DO - 10.1016/j.bbapap.2009.08.001
M3 - Article
C2 - 19665595
AN - SCOPUS:69249216528
SN - 1570-9639
VL - 1794
SP - 1288
EP - 1298
JO - Biochimica et Biophysica Acta - Proteins and Proteomics
JF - Biochimica et Biophysica Acta - Proteins and Proteomics
IS - 9
ER -