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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
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We are analyzing https://link.springer.com/article/10.1007/s10822-008-9168-9.

Title:
Multiple protein structures and multiple ligands: effects on the apparent goodness of virtual screening results | Journal of Computer-Aided Molecular Design
Description:
As an extension to a previous published study (McGaughey et al., J Chem Inf Model 47:1504–1519, 2007) comparing 2D and 3D similarity methods to docking, we apply a subset of those virtual screening methods (TOPOSIM, SQW, ROCS-color, and Glide) to a set of protein/ligand pairs where the protein is the target for docking and the cocrystallized ligand is the target for the similarity methods. Each protein is represented by a maximum of five crystal structures. We search a diverse subset of the MDDR as well as a diverse small subset of the MCIDB, Merck’s proprietary database. It is seen that the relative effectiveness of virtual screening methods, as measured by the enrichment factor, is highly dependent on the particular crystal structure or ligand, and on the database being searched. 2D similarity methods appear very good for the MDDR, but poor for the MCIDB. However, ROCS-color (a 3D similarity method) does well for both databases.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Technology & Computing
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

The income method remains a mystery to us.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com might be cashing in, but we can't detect the method they're using.

Keywords {🔍}

article, chem, cas, google, scholar, screening, docking, virtual, molecular, inf, similarity, sheridan, model, methods, protein, med, search, privacy, cookies, content, journal, research, mcgaughey, access, comput, data, information, publish, design, multiple, effects, cornell, glide, scoring, sci, approach, log, computeraided, structures, goodness, published, robert, metrics, study, subset, ligand, database, databases, structurebased, discover,

Topics {✒️}

month download article/chapter fingerprint-based similarity search computer-aided hit discovery screening drug multiple protein structures protein/ligand pairs structure-based structure-activity studies 3d similarity methods 2d similarity methods 3d similarity method virtual screening results virtual screening methods molecular design shape-based tools full article pdf privacy choices/manage cookies crystal structure protein flexibility comparing 2d previous published study virtual screening related subjects merck research laboratories molecular docking screens topological similarity searches molecular docking accuracy chemical databases chem inf model high-throughput docking european economic area immuno oncology library electronic supplementary material instant access conditions privacy policy gaussian docking functions early recognition problem article sheridan protein rocs-color similarity methods check access article journal accepting optional cookies toposim sqw machine learning physiochemical property descriptors sq journal finder publish

Schema {🗺️}

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         description:As an extension to a previous published study (McGaughey et al., J Chem Inf Model 47:1504–1519, 2007) comparing 2D and 3D similarity methods to docking, we apply a subset of those virtual screening methods (TOPOSIM, SQW, ROCS-color, and Glide) to a set of protein/ligand pairs where the protein is the target for docking and the cocrystallized ligand is the target for the similarity methods. Each protein is represented by a maximum of five crystal structures. We search a diverse subset of the MDDR as well as a diverse small subset of the MCIDB, Merck’s proprietary database. It is seen that the relative effectiveness of virtual screening methods, as measured by the enrichment factor, is highly dependent on the particular crystal structure or ligand, and on the database being searched. 2D similarity methods appear very good for the MDDR, but poor for the MCIDB. However, ROCS-color (a 3D similarity method) does well for both databases.
         datePublished:2008-02-14T00:00:00Z
         dateModified:2008-02-14T00:00:00Z
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      description:As an extension to a previous published study (McGaughey et al., J Chem Inf Model 47:1504–1519, 2007) comparing 2D and 3D similarity methods to docking, we apply a subset of those virtual screening methods (TOPOSIM, SQW, ROCS-color, and Glide) to a set of protein/ligand pairs where the protein is the target for docking and the cocrystallized ligand is the target for the similarity methods. Each protein is represented by a maximum of five crystal structures. We search a diverse subset of the MDDR as well as a diverse small subset of the MCIDB, Merck’s proprietary database. It is seen that the relative effectiveness of virtual screening methods, as measured by the enrichment factor, is highly dependent on the particular crystal structure or ligand, and on the database being searched. 2D similarity methods appear very good for the MDDR, but poor for the MCIDB. However, ROCS-color (a 3D similarity method) does well for both databases.
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      dateModified:2008-02-14T00:00:00Z
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External Links {🔗}(69)

Analytics and Tracking {📊}

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