| URL: | http://www.idrtech.com/PDB-Ligand/ |
| Full name: | |
| Description: | PDB-Ligand is a three-dimensional structure database of small molecular ligands that are bound to larger biomolecules deposited in the Protein Data Bank (PDB). |
| Year founded: | 2005 |
| Last update: | 2005-01-01 |
| Version: | |
| Accessibility: |
Unaccessible
|
| Country/Region: | Korea, Republic of |
| Data type: | |
| Data object: |
|
| Database category: | |
| Major species: |
|
| Keywords: |
| University/Institution: | IDR Tech. |
| Address: | IDR Tech. B-3003 Tripolis, 210 KumGok-Dong, BunDang-Ku, SungNam-Shi, KyungKi-Do, Republic of Korea |
| City: | KyungKi-Do |
| Province/State: | |
| Country/Region: | Korea, Republic of |
| Contact name (PI/Team): | Jae-Min Shin |
| Contact email (PI/Helpdesk): | jms@idrtech.com |
|
PDB-Ligand: a ligand database based on PDB for the automated and customized classification of ligand-binding structures. [PMID: 15608186]
PDB-Ligand (http://www.idrtech.com/PDB-Ligand/) is a three-dimensional structure database of small molecular ligands that are bound to larger biomolecules deposited in the Protein Data Bank (PDB). It is also a database tool that allows one to browse, classify, superimpose and visualize these structures. As of May 2004, there are about 4870 types of small molecular ligands, experimentally determined as a complex with protein or DNA in the PDB. The proteins that a given ligand binds are often homologous and present the same binding structure to the ligand. However, there are also many instances wherein a given ligand binds to two or more unrelated proteins, or to the same or homologous protein in different binding environments. PDB-Ligand serves as an interactive structural analysis and clustering tool for all the ligand-binding structures in the PDB. PDB-Ligand also provides an easier way to obtain a number of different structure alignments of many related ligand-binding structures based on a simple and flexible ligand clustering method. PDB-Ligand will be a good resource for both a better interpretation of ligand-binding structures and the development of better scoring functions to be used in many drug discovery applications. |