Datasets from the Buschiazzo Laboratory



X-Ray Diffraction data from Leptospira interrogans Flagellar-coiling protein B (FcpB), source of 6NQZ structure

iodide + magic triangle soaking, SAD data set (@1.5418 angstroms wavelength) These data were used to refine the structure (but not for structure solution, for which a separate data set was used, and deposited under #694)

X-Ray Diffraction data from Leptospira interrogans Flagellar-coiling protein B (FcpB), source of 6NQZ structure

iodide + magic triangle soaking, SAD data set (@1.5418 angstroms wavelength) These data were used to solve the structure by direct methods using the iodine atoms as anomalous scatterers (but not for final refinement, for which a separate data set has been used and deposited)

X-Ray Diffraction data from Leptospira biflexa Flagellar-coiling protein A (FcpA), source of 6NQW structure

native data set (hexagonal P622 form of FcpA from L. biflexa)

X-Ray Diffraction data from Leptospira biflexa Flagellar-coiling protein A (FcpA), source of 6NQY structure

Iodine quick-soak - SAD data set (monoclinic C2 form of FcpA from L. biflexa)

X-Ray Diffraction data from Leptospira biflexa Flagellar-coiling protein A (FcpA), source of 6NQX structure

Native data set (monoclinic form of FcpA from L. biflexa)

X-Ray Diffraction data from FasR transcription factor from Mycobacterium tuberculosis in complex with DNA, source of 6O6P structure

Native dataset ; low resolution, but best data so far with these orthorhombic crystals

X-Ray Diffraction data from FasR transcription factor from Mycobacterium tuberculosis, source of 6O6O structure

Native data; the protein was not co-crystallized or soaked with any ligand, but turned out to contain myristic acid bound, coming from the expression system

X-Ray Diffraction data from FasR transcription factor from Mycobacterium tuberculosis in complex with C20-CoA, source of 6O6N structure

Native data, phased ab-initio using Arcimboldo

X-Ray Diffraction data from Catalase HPII from E. coli, source of 6BY0 structure

Native dataset

X-Ray Diffraction data from Complex DesKC:DesR-REC (B. subtilis) - phosphotransferase state, high Mg2+ & BeF3-, source of 5IUL structure

native dataset

X-Ray Diffraction data from Phosphorylated DesKC (B. subtilis), source of 5IUM structure

Native dataset

X-Ray Diffraction data from Complex DesKC:DesR-REC (B. subtilis) - phosphotransferase state, high Mg2+, source of 5IUK structure

Native dataset

X-Ray Diffraction data from Complex DesKC:DesR-REC (B. subtilis) - phosphatase state, source of 5IUN structure

Native dataset

X-Ray Diffraction data from Complex DesKC:DesR-REC (B. subtilis) - phosphotransferase state, low Mg2+, source of 5IUJ structure

Native dataset

X-Ray Diffraction data from capsid protein (N-terminal domain) from Bovine Leukemia Virus, source of 4PH3 structure

immature NTD domain (one extra residue at the N-terminus, before the mature Pro) / SAD dataset (quick iodide soak) collected at Cu Ka wavelength

X-Ray Diffraction data from capsid protein (C-terminal domain) from Bovine Leukemia Virus, source of 4PH1 structure

native data set

X-Ray Diffraction data from capsid protein (N-terminal domain) from Bovine Leukemia Virus, source of 4PH2 structure

mature NTD domain / native data

X-Ray Diffraction data from capsid protein from Bovine Leukemia Virus, source of 4PH0 structure

native (non-engineered) construct of full-length capsid