MODBASE, a database of annotated comparative protein structure models and associated resources
Open Access
- 1 January 2009
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 37 (Database), D347-D354
- https://doi.org/10.1093/nar/gkn791
Abstract
MODBASE (http://salilab.org/modbase) is a database of annotated comparative protein structure models. The models are calculated by MODPIPE, an automated modeling pipeline that relies primarily on MODELLER for fold assignment, sequence-structure alignment, model building and model assessment (http:/salilab.org/modeller). MODBASE currently contains 5 152 695 reliable models for domains in 1 593 209 unique protein sequences; only models based on statistically significant alignments and/or models assessed to have the correct fold are included. MODBASE also allows users to calculate comparative models on demand, through an interface to the MODWEB modeling server (http://salilab.org/modweb). Other resources integrated with MODBASE include databases of multiple protein structure alignments (DBAli), structurally defined ligand binding sites (LIGBASE), predicted ligand binding sites (AnnoLyze), structurally defined binary domain interfaces (PIBASE) and annotated single nucleotide polymorphisms and somatic mutations found in human proteins (LS-SNP, LS-Mut). MODBASE models are also available through the Protein Model Portal (http://www.proteinmodelportal.org/).This publication has 62 references indexed in Scilit:
- Global Sequencing of Proteolytic Cleavage Sites in Apoptosis by Specific Labeling of Protein N TerminiCell, 2008
- Database resources of the National Center for Biotechnology InformationNucleic Acids Research, 2007
- Structure-based activity prediction for an enzyme of unknown functionNature, 2007
- The Universal Protein Resource (UniProt)Nucleic Acids Research, 2006
- Protein complex compositions predicted by structural similarityNucleic Acids Research, 2006
- UCSF Chimera—A visualization system for exploratory research and analysisJournal of Computational Chemistry, 2004
- Statistical potentials for fold assessmentProtein Science, 2002
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Comparative Protein Modelling by Satisfaction of Spatial RestraintsJournal of Molecular Biology, 1993
- Dictionary of protein secondary structure: Pattern recognition of hydrogen‐bonded and geometrical featuresBiopolymers, 1983