Site Lookup:
Government Agency Domains
Select domain(s) that contain a specific agency name(s) in the URL
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Title: |
Decontamination and Decommissioning (D&D;) of Nuclear Facilities [Safe and cost-effective decommissioning of surplus, radiologically
contaminated facilities]
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Archival URL:
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http://eot.us.archive.org/eot/20170131194524/http://dd.anl.gov/ |
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Live URL: |
http://dd.anl.gov/ |
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Coverage: |
December 21, 2016 - January 31, 2017 |
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Description: |
The Decontamination and Decommissioning (D&D) Operations of the Argonne NE Division conducts the safe and cost-effective decommissioning
of surplus, radioactively contaminated facilities. This work involves project identification, design, planning, budgeting,
and project execution including disassembly, size reduction, waste packaging, demolition and decontamination. Knowledge gained
through successful project completions is shared with others in the DOE complex and the nuclear community at large through
topical presentations, training, and exchange of lessons learned.
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Title: |
General Automated Atomic Model Parameterization
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Archival URL:
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http://eot.us.archive.org/eot/20161118004241/http://gaamp.lcrc.anl.gov/ |
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Live URL: |
http://gaamp.lcrc.anl.gov/ |
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Coverage: |
November 18, 2016 - November 18, 2016 |
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Description: |
One of the key concepts in the design of the present Consortium is out ability to rationalize through computational means
a vast amount of static and dynamics structural data with functional information. The computational Core is designed to generate,
implement, validate and distribute state-of-the-art “tools” required for the studies of complex membrane protein systems.
This includes expertise and services of well-established tools, novel methods and technologies that will support the experimental
studies, such as methods for analysis of spectroscopic data, and ground work on basic computational staples like force fields
and biomolecular simulations. All the computational methodologies will be readily made available to the broader scientific
community through our website. From the outset, Cores will have pre-set interactions with the different projects as depicted
in Figure 4. By design, two Cores will necessarily have a direct impact in the development of all bridging (and pilot) projects.
These are Core D1 (Protein expression and purification), which will have a hand in securing purified material and mutants
for biophysical measurements and functional reconstitution, and Core D4 (Computational and Modeling resource), which will
help to put into mechanistic and energetic perspective the vast amounts of data we expect to collect. Roux, Bahar, Schulten,
Tajkhorshid, Weinstein Figure Caption: Pseudo-atoms representing the spin label attached to each residue, are shown for
one subunit and color coded as follows: red particles represent buried residues, blue cles represent aqueous residues, yellow
particles represent residues facing the membrane, and green particles represent residues at the water-membrane interface.
Red les are shown for each Cα atom representing PROT particles attached to each residue. Inset shows protein residues in thin
licorice representation and pseudospin probes in CPK representation. Unbounded particles in red and blue represent O2 and
NiEdda virtual environment particles, respectively. View of the NH2-terminal model after pseudoatom-driven solvent accessibility
refinement is shown on the right panel. Residues 1 to 28 are shown in gray; resultant vectors for NiEdda and O2 accessibilities
are shown in blue and red, respectively. Taken from Vasquez et al. J Mol Biol 378:55-70, 2008).
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