The Structure–Function Linkage Database

Autor: Shoshana D. Brown, John H. Morris, Patricia C. Babbitt, Alexandra M. Schnoes, Ashley F. Custer, Gemma L. Holliday, Susan T. Mashiyama, Jeffrey M. Yunes, Alan E. Barber, Florian Lauck, Michael A. Hicks, Doug Stryke, Thomas E. Ferrin, Elaine C. Meng, Eyal Akiva, Sunil Ojha, Conrad C. Huang, David Mischel, Daniel Almonacid
Přispěvatelé: Massachusetts Institute of Technology. Department of Chemical Engineering, Hicks, Michael A.
Rok vydání: 2013
Předmět:
Zdroj: Nucleic Acids Research
Akiva, E; Brown, S; Almonacid, DE; Barber, AE; Custer, AF; Hicks, MA; et al.(2014). The Structure-Function Linkage Database. Nucleic Acids Research, 42(D1), D521-D530. doi: 10.1093/nar/gkt1130. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/3bf997bt
Nucleic acids research, vol 42, iss Database issue
Oxford University Press
ISSN: 1362-4962
0305-1048
DOI: 10.1093/nar/gkt1130
Popis: The Structure-Function Linkage Database (SFLD, http://sfld.rbvi.ucsf.edu/) is a manually curated classification resource describing structure-function relationships for functionally diverse enzyme superfamilies. Members of such superfamilies are diverse in their overall reactions yet share a common ancestor and some conserved active site features associated with conserved functional attributes such as a partial reaction. Thus, despite their different functions, members of these superfamilies 'look alike', making them easy to misannotate. To address this complexity and enable rational transfer of functional features to unknowns only for those members for which we have sufficient functional information, we subdivide superfamily members into subgroups using sequence information, and lastly into families, sets of enzymes known to catalyze the same reaction using the same mechanistic strategy. Browsing and searching options in the SFLD provide access to all of these levels. The SFLD offers manually curated as well as automatically classified superfamily sets, both accompanied by search and download options for all hierarchical levels. Additional information includes multiple sequence alignments, tab-separated files of functional and other attributes, and sequence similarity networks. The latter provide a new and intuitively powerful way to visualize functional trends mapped to the context of sequence similarity. © 2013 The Author(s). Published by Oxford University Press.
Databáze: OpenAIRE