Structure Alignment in Polynomial Time Rachel Kolodny Stanford University Nati Linial The Hebrew University of Jerusalem

Problem Statement 2 structures in R 3 A={a 1,a 2,…,a n }, B={b 1,b 2,…,b m } Find subsequences s a and s b s.t the substructures {a s a (1),a s a (2),…, a s a (l) },{b s b (1),b s b (2),…, b s b (l) } are similar

Motivation Structure is better conserved than amino acid sequence –Structure similarity can give hints to common functionality/origin Allows automatic classification of protein structure

Correspondence  Position Given a correspondence the rotation and translation that minimize the cRMS distance can be calculated Kabsch, W. (1978).

Position  Correspondence Given a rotation and translation one can calculate the alignment that optimizes a (separable) score –Using dynamic programming –Essentially similar to sequence alignment Example score

Score  cRMS We want to give “bonus points” for longer correspondences –e.g. corresponding ONE atom from each structure has 0 cRMS Even better scores ? –vary gap penalty depending on position in structure –Incorporate sequence information

Score  cRMS A specific correspondence

Previous Work Distance MatricesHeuristics in rotation and translation space DALI [Holm and Sander 93] CONGENEAL [Yee & Dill 93] SSAP [Taylor & Orengo 89] Nussinov-Wolfson [89,93] Godzik [93] … STRUCTAL [Subibiah et al 93] COMPARER [Sali & Blundell 90] LOCK [Singh & Brutlag 97] CE [Shindyalov & Bourne 98] Taylor (??) [93] Zu-Kang & Sipppl 96 (?) … *most data taken from Orengo 94

“…It can be proved that, for these reasons, finding an optimal structural alignment between two protein structures is an NP hard problem and thus there are no fast structural alignment algorithms that are guaranteed to be optimal within any given similarity measure…” Adam Godzik ‘The structural alignment between two proteins: Is there a unique answer’ 1996 “There is no exact solution to the protein structure alignment problem, only the best solution for the heuristics used in the calculation.” Shindyalov & Bourne ‘Protein Structure Alignment by Incremental Combinatorial (CE) of the Optimal Path’ 1998

Exponentially many Focus on Scoring Functions

Exponentially many Focus on Scoring Functions

Exponentially many All Maxima are interesting Noisy data !!

Good scoring functions Each of the functions is well-behaved –Satisfies Lipschitz condition Thus, the maximum over a finite set is well-behaved In each dimension two points at distance  have function values that vary by O(n  ) Need O(n) samples in every dimension

Sampling is Sufficient

Polynomial Algorithm Sample in rotation and translation space –compute best score (and alignment) for each sample point Return maximum score Need O(n 6 n 2 ) time and O(n 2 ) space

Internal Distance Matrices Invariant to position and rotation of structures  can be compared directly Find largest common sub-matrices (LCM) whose distances are roughly the same

LCM is NP-complete Harder than MAX- CLIQUE Matrices encode distances that are positive, symmetric and obey triangle inequality

Example 1dme 28 amino acids 1jjd 51 amino acids Best STRUCTAL score 149 Best score found by exhaustive search 197

Heuristic Consider only translations that positions an atom from protein A on an atom of protein B O(m*n) instead of O((n+m) 3 )