Maintance Thur 2026 Nov 12

The SBDB will be undergoing infrastructure maintance Thur 2026 Nov 12 between 10AM and 6PM ET. Dataset registrations, dataset depositions, and dataset downloads from the primary location will be unavailable; API access will also be impacted.




Datasets from the Buschiazzo Laboratory




X-Ray Diffraction data from Legionella pneumophila DOT1L methyltransferase, source of structure

Native data of LpDot1 in complex with S-adenosyl homocysteine


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