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AutoCAD® Civil 3D® software is a Building Information Modeling (BIM) solution for civil engineering design and documentation. Civil 3D is built for civil engineers, drafters, designers, and technicians working on transportation, land development, and water projects. Stay coordinated and explore design options, analyze project performance, and deliver more consistent, higher-quality documentation—all within a familiar AutoCAD® software environment. Features AutoCAD® Civil 3D® 2013 civil engineering software extends the value of your model with new workflows and productivity tools for civil infrastructure. With a focus on optimizing performance, the new features offer pressure pipe functionality, improved survey, base map creation, and new rail track design features. And, a host of transportation features have been enhanced, including corridor composition workflows, 3D navigation and interrogation, and surface boundary definition.
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Streamline your civil engineering projects with AutoCAD Civil 3D software. Pressure Networks AutoCAD Civil 3D 2013 features pressure pipe modeling tools, enabling you to: create and distribute pipe; add fitting and appurtenance content; model pressure networks in 2D and 3D; and leverage 3D pressure networks for interference checking. Survey AutoCAD Civil 3D 2013 features a number of new capabilities that streamline survey workflows for civil engineering projects resulting in greater flexibility. You can query survey data for the creation of Civil 3D surfaces, point groups, and drafted survey figures. Usability improvements enable you to label survey figures, label between two graphical points, and control linetype display. Transportation Beyond a variety of scalability and performance improvements for civil engineering projects, AutoCAD Civil 3D 2013 offers a streamlined workflow for creating corridor models. Enhancements include usability improvements for creating and editing corridor assemblies and the inclusion of Autodesk® Subasse.
The regulatory protein NsrR, a member of the Rrf2 family of transcription repressors, is specifically dedicated to sensing nitric oxide (NO) in a variety of pathogenic and non-pathogenic bacteria. It has been proposed that NO directly modulates NsrR activity by interacting with a predicted [Fe-S] cluster in the NsrR protein, but no experimental evidence has been published to support this hypothesis.
Here we report the purification of NsrR from the obligate aerobe Streptomyces coelicolor. We demonstrate using UV-visible, near UV CD and EPR spectroscopy that the protein contains an NO-sensitive [2Fe-2S] cluster when purified from E. Upon exposure of NsrR to NO, the cluster is nitrosylated, which results in the loss of DNA binding activity as detected by bandshift assays. Removal of the [2Fe-2S] cluster to generate apo-NsrR also resulted in loss of DNA binding activity. This is the first demonstration that NsrR contains an NO-sensitive [2Fe-2S] cluster that is required for DNA binding activity. Introduction Nitric oxide (NO) is a highly reactive and toxic free radical gas that can freely diffuse into cells and attack the redox centers of proteins. Human macrophages produce NO as a very early line of defense against invading bacterial pathogens.
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