Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

6OBY

The nucleotide-binding protein AF_226 in complex with ADP from Archaeoglobus fulgidus with Co found by PIXE. Based on 3KB1.

Summary for 6OBY
Entry DOI10.2210/pdb6oby/pdb
DescriptorIron-sulfur cluster carrier protein, ADENOSINE-5'-DIPHOSPHATE, COBALT (II) ION, ... (4 entities in total)
Functional Keywordsalpha-beta protein, pixe, metal transport
Biological sourceArchaeoglobus fulgidus
Total number of polymer chains2
Total formula weight59839.28
Authors
Snell, E.H.,Garman, E.F.,Lowe, E.D. (deposition date: 2019-03-21, release date: 2019-12-25, Last modification date: 2020-01-22)
Primary citationGrime, G.W.,Zeldin, O.B.,Snell, M.E.,Lowe, E.D.,Hunt, J.F.,Montelione, G.T.,Tong, L.,Snell, E.H.,Garman, E.F.
High-Throughput PIXE as an Essential Quantitative Assay for Accurate Metalloprotein Structural Analysis: Development and Application.
J.Am.Chem.Soc., 142:185-197, 2020
Cited by
PubMed Abstract: Metalloproteins comprise over one-third of proteins, with approximately half of all enzymes requiring metal to function. Accurate identification of these metal atoms and their environment is a prerequisite to understanding biological mechanism. Using ion beam analysis through particle induced X-ray emission (PIXE), we have quantitatively identified the metal atoms in 30 previously structurally characterized proteins using minimal sample volume and a high-throughput approach. Over half of these metals had been misidentified in the deposited structural models. Some of the PIXE detected metals not seen in the models were explainable as artifacts from promiscuous crystallization reagents. For others, using the correct metal improved the structural models. For multinuclear sites, anomalous diffraction signals enabled the positioning of the correct metals to reveal previously obscured biological information. PIXE is insensitive to the chemical environment, but coupled with experimental diffraction data deposited alongside the structural model it enables validation and potential remediation of metalloprotein models, improving structural and, more importantly, mechanistic knowledge.
PubMed: 31794207
DOI: 10.1021/jacs.9b09186
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.87 Å)
Structure validation

226707

건을2024-10-30부터공개중

PDB statisticsPDBj update infoContact PDBjnumon