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Journal of Molecular Modeling (Record no. 1501)

MARC details
000 -LEADER
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001 - CONTROL NUMBER
control field 0948-5023
003 - CONTROL NUMBER IDENTIFIER
control field DE-He213
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260610082450.0
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
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008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
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022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0948-5023
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/894.0948-5023
Source of number or code doi
210 10 - ABBREVIATED TITLE
Abbreviated title J Mol Model
245 10 - TITLE STATEMENT
Title Journal of Molecular Modeling
Medium [electronic resource] :
Remainder of title Computational Chemistry - Life Science - Advanced Materials - New Methods /
Statement of responsibility, etc. edited by Timothy Clark.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Berlin/Heidelberg :
Name of producer, publisher, distributor, manufacturer Springer Berlin Heidelberg :
-- Imprint: Springer.
300 ## - online resource
Other physical details online resource.
520 ## - SUMMARY, ETC.
Summary, etc. The Journal of Molecular Modeling publishes high quality specialized 3D molecular modeling studies that pass peer review and fall within the scope of the journal. Because of the number of manuscripts submitted to the journal and the high rejection rate, the following guidelines are provided to help assess your own work: Computer-Aided Drug Design Computer-aided molecular design, rational drug design, de novo ligand design, receptor modeling and docking, molecular-dynamics simulations used for drug design. Manuscripts that report new methodology are welcome, as are those that report new techniques and their validation. Extensive validation on a number of diverse datasets is necessary. Studies that use commercially available techniques or web services for docking, ADMET evaluation or MD simulations are discouraged. Protein structures used for docking studies must be equilibrated adequately using MD simulations of at least 500 ns. At least 3 different conformations of the target (from multiple crystal structures or generated using an MD simulation of at least 500ns) must be used to generate consensus poses for docking studies. Docked poses must again be proved stable using at least three MD simulations, each of at least 300 ns, or a single simulation of at least 500ns. MD simulations should be analyzed to identify key interactions and provide a binding model for predictive drug design. Simply testing the short-term stability of the docked pose using RSMD or radius of gyration is discouraged. Life Science Modeling Homology modeling Homology models are welcome if they are validated by adequate MD simulations (at least 500 ns). Simulation of proteins, DNA, carbohydrates and other biopolymers Manuscripts that provide mechanistic insights or offer novel interpretation of the experimental data are welcome. Molecular-dynamics simulations must be run for at least 500ns and in triplicate (or correspondingly longer single simulations) and sampling convergence demonstrated. Modeling biological reaction mechanisms Modeling studies of biological reaction mechanisms are welcome. Protein flexibility must be taken into account. Combined experimental/computational studies in which calculations play a dominant role Manuscripts that place the main emphasis on the calculations and use them to provide information not available from experiment are welcome. Manuscripts in which standard calculations are used as an adjunct to an otherwise experimental study are discouraged. Please do not hesitate to contact the editorial office if you are in doubt as to whether your work falls within the scope of the Journal.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chemistry—Data processing.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Medicine—Research.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Biology—Research.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Bioinformatics.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Materials—Analysis.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chemistry, Physical and theoretical.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Computational Chemistry.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Biomedical Research.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Computational and Systems Biology.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Characterization and Analytical Technique.
650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Theoretical Chemistry.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Clark, Timothy.
Relator term editor.
Relationship edt
-- http://id.loc.gov/vocabulary/relators/edt
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element SpringerLink (Online service)
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Printed version:
International Standard Serial Number 1610-2940
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1007/894.0948-5023">https://doi.org/10.1007/894.0948-5023</a>
Public note Hybrid

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