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Classification: understanding the diversity and principles of. protein structure and function. Tool: structure comparison. MCSG 2001 structures. Why compare protein structures?. Learn about – structure-function relationships – evolution – common building blocks – motifs
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Classification: understanding the diversity and principles of protein structure and function Tool: structure comparison MCSG 2001 structures
Why compare protein structures? • Learn about – structure-function relationships – evolution – common building blocks – motifs • Make order out of the universe of protein structures • Help structure prediction Inge Jonassen
Structure Comparison Growth factor Cytokine • Evolutionary relationship • Structure classification
9% sequence identity Shapiro & Harris, 2000
Strategies • Bottom Up find local matches first, then solve the combinatorial problem to identify the largest cluster of matching substructures (e.g., Dali, CE, etc.) • Top Down find a rough global alignment first, then use a refinement procedure to identify details of local matches (e.g., 3D look-up, subgraph isomorphism, etc.)
Types of substructure used • Atom/atom group • Residue • Fragment • Secondary structure element (SSE) • Structure described by elements of the chosen type (e.g. molecular surface)
3D Lookup Holm & Sander (1995)
Structure Comparison Tools • DALI ( http://www2.ebi.ac.uk/dali/ ) • CE ( http://cl.sdsc.edu/ ) • VAST (http://www.ncbi.nlm.nih.gov/Structure/VAST/vast.html ) • Prosup ( http://www.came.sbg.ac.at ) • FLASH (http://thr.ibms.sinica.edu.tw/flash/)
Results of different methods on the comparison of Azurin (1azc:A) vs plastocyanin (1plc)
Circular Permutation (CP) B N A C B A C N C D C D ..A..B..C..D.. ..C..D..A..B..
A real example of CP C N N C 1nls (Concanavalin) 1led (Lectin)
FLASH’s algorithm SSE matching: Angle-distance map:
Greedy selection of distinct alignment solutions (1) g - f’ d - c’f - e’ e - d’ b - a’ c - b’ (2) c - e’ b - d’d - f’ (3) e - a’ f - b’g - c’ Optimal: Alternative:
N C’ C N’ N C A B C D N’ C’ A D C B Scrambled Protein Pair “…few, if any, are able to detect permutations directly.” - Robert B. Russell (2002)
Unique Capabilities: • alternative alignments allowing sub-domain motif (structural building block) discovery • permutation detection at all levels of complexity