The ligand interaction workflow allow a user to upload a PDB file and get an analysis of protein-ligand interactions in the complex.
Site search - manual
The site search tool allows a user to search a set of receptors for a sequence motif consisting of residue positions and chemical properties. Using the tools is a two step process.
The user is first presented with a receptor selection page. Receptors can be selected individually or by family. The user can select as many receptors as he/she wishes (WARNING: selecting a large number of receptors increases loading time).
After receptors have been selected, the user is presented with a sequence motif selection page. Site residues should be selected individually. Clicking the down arrow button next to a sequence segment will expand the residues within that segment. Chemical features (Hydrophobic, hydrogen bond donor, etc.) should then be selected for each motif residue. When a feature has been selected, a list of amino acids that match the feature will appear to the right of the residue.
The selected residues can be organised into separate interactions. An interaction can contain one or more residues. To add an interaction, click the 'Add interaction' button. Selected residues will be added to the currently active interaction (shown in bold text). To change the active interaction, click on the name of the interaction. Within an interaction, the number of residues required to match can be specified in the 'Min. match' selection box.
After completing these two steps, an alignment is displayed. The sequences of the selected receptors are split into "Matching sequences" and "Non-matching sequences", according to their match of the selected site. To display the sequence number of an aligned residue, as well as generic number indices, hover the mouse over it.
Site search - from pdb complex
This is a variant of the manual site search tool, where the user can upload a PDB structure and have protein-ligand interactions automatically detected and translated into a site search. After interactions have been detected, the user can edit the definition, and continue as in a manual search.
The tool is based on the following paper:
K Fidom, V Isberg, A Hauser, S Mordalski, T Lehto, AJ Bojarski, DE Gloriam, "A New Crystal Structure Fragment-Based Pharmacophore Method for G Protein-Coupled Receptors", 2015, Methods, 71, 104–112. 10.1016/j.ymeth.2014.09.009
We have developed a new method for the building of pharmacophores for G protein-coupled receptors, a major drug target family. The method is a combination of the ligand- and target-based pharmacophore methods and founded on the extraction of structural fragments, interacting ligand moiety and receptor residue pairs, from crystal structure complexes. We describe the procedure to collect a library with more than 250 fragments covering 29 residue positions within the generic transmembrane binding pocket. We describe how the library fragments are recombined and inferred to build pharmacophores for new targets. A validating retrospective virtual screening of histamine H1 and H3 receptor pharmacophores yielded area-under-the-curves of 0.88 and 0.82, respectively. The fragment-based method has the unique advantage that it can be applied to targets for which no (homologous) crystal structures or ligands are known. 47% of the class A G protein-coupled receptors can be targeted with at least four-element pharmacophores. The fragment libraries can also be used to grow known ligands or for rotamer refinement of homology models. Researchers can download the complete fragment library or a subset matching their receptor of interest using our new tool in GPCRdb.
Sodium ion site
In many GPCRs, a sodium ion acts as an allosteric modulator stabilising the inactive state. The sodium ion site involves a number of direct and indirect polar interactions. The receptor residues D2x50 and S3x39 are known to interact frequently and directly with the sodium ion, and mutation of these residues causes loss of G protein mediated signalling (White et al., Structure, 2018; 10.1016/j.str.2017.12.013). In the "Structure Browser" under the "Receptors" menu, users can find a "Sodium ion site" column section with two columns. The first shows whether D2x50 and S3x39 are present in the wild type sequence of the structure, the second shows whether there is a sodium ion interacting with the two residues in the given structure.