Record updated: Sept. 27, 2016, 11:28 a.m. by The FAIRsharing Team.

Edits to 'https://fairsharing.org/FAIRsharing.etqbej' by 'The FAIRsharing Team' at 11:28, 27 Sep 2016 (approved):

	'description' has been modified:
		Before: POcket Similarity Search Using Multiple-Sketches  (PoSSuM) includes all the discovered protein-small molecule binding site pairs with annotations of various types (e.g., UniProt, CATH, SCOP, SCOPe, EC number and Gene ontology). PoSSuM enables rapid exploration of similar binding sites among structures with different global folds as well as similar folds. Moreover, PoSSuM is useful for predicting the binding ligand for unbound structures. 
		After: POcket Similarity Search Using Multiple-Sketches (PoSSuM) includes all the discovered protein-small molecule binding site pairs with annotations of various types (e.g., UniProt, CATH, SCOP, SCOPe, EC number and Gene ontology). PoSSuM enables rapid exploration of similar binding sites among structures with different global folds as well as similar folds. Moreover, PoSSuM is useful for predicting the binding ligand for unbound structures. 

            

Edits to 'https://fairsharing.org/FAIRsharing.etqbej' by 'The FAIRsharing Team' at 14:28, 26 Sep 2016 (approved):

	'description' has been modified:
		Before: POcket Similarity Search Using Multiple-Sketches Pocket Similarity Search using Multiple-Sketches (PoSSuM) includes all the discovered protein-small molecule binding site pairs with annotations of various types (e.g., UniProt, CATH, SCOP, SCOPe, EC number and Gene ontology). PoSSuM enables rapid exploration of similar binding sites among structures with different global folds as well as similar folds. Moreover, PoSSuM is useful for predicting the binding ligand for unbound structures. 
		After: POcket Similarity Search Using Multiple-Sketches  (PoSSuM) includes all the discovered protein-small molecule binding site pairs with annotations of various types (e.g., UniProt, CATH, SCOP, SCOPe, EC number and Gene ontology). PoSSuM enables rapid exploration of similar binding sites among structures with different global folds as well as similar folds. Moreover, PoSSuM is useful for predicting the binding ligand for unbound structures.