TY - JOUR

T1 - Estimating the probability for a protein to have a new fold

T2 - A statistical computational model

AU - Portugaly, Elon

AU - Linial, Michal

PY - 2000/5/9

Y1 - 2000/5/9

N2 - Structural genomics aims to solve a large number of protein structures that represent the protein space. Currently an exhaustive solution for all structures seems prohibitively expensive, so the challenge is to define a relatively small set of proteins with new, currently unknown folds. This paper presents a method that assigns each protein with a probability of having an unsolved fold. The method makes extensive use of PROTOMAP, a sequence-based classification, and SCOP, a structure-based classification. According to PROTOMAP, the protein space encodes the relationship among proteins as a graph whose vertices correspond to 13,354 clusters of proteins. A representative fold for a cluster with at least one solved protein is determined after superposition of all SCOP (release 1.37) folds onto PROTOMAP clusters. Distances within the PROTOMAP graph are computed from each representative fold to the neighboring folds. The distribution of these distances is used to create a statistical model for distances among those folds that are already known and those that have yet to be discovered. The distribution of distances for solved/unsolved proteins is significantly different. This difference makes it possible to use Bayes' rule to derive a statistical estimate that any protein has a yet undetermined fold. Proteins that score the highest probability to represent a new fold constitute the target list for structural determination. Our predicted probabilities for unsolved proteins correlate very well with the proportion of new folds among recently solved structures (new SCOP 1.39 records) that are disjoint from our original training set.

AB - Structural genomics aims to solve a large number of protein structures that represent the protein space. Currently an exhaustive solution for all structures seems prohibitively expensive, so the challenge is to define a relatively small set of proteins with new, currently unknown folds. This paper presents a method that assigns each protein with a probability of having an unsolved fold. The method makes extensive use of PROTOMAP, a sequence-based classification, and SCOP, a structure-based classification. According to PROTOMAP, the protein space encodes the relationship among proteins as a graph whose vertices correspond to 13,354 clusters of proteins. A representative fold for a cluster with at least one solved protein is determined after superposition of all SCOP (release 1.37) folds onto PROTOMAP clusters. Distances within the PROTOMAP graph are computed from each representative fold to the neighboring folds. The distribution of these distances is used to create a statistical model for distances among those folds that are already known and those that have yet to be discovered. The distribution of distances for solved/unsolved proteins is significantly different. This difference makes it possible to use Bayes' rule to derive a statistical estimate that any protein has a yet undetermined fold. Proteins that score the highest probability to represent a new fold constitute the target list for structural determination. Our predicted probabilities for unsolved proteins correlate very well with the proportion of new folds among recently solved structures (new SCOP 1.39 records) that are disjoint from our original training set.

UR - http://www.scopus.com/inward/record.url?scp=0034625049&partnerID=8YFLogxK

U2 - 10.1073/pnas.090559497

DO - 10.1073/pnas.090559497

M3 - Article

C2 - 10792051

AN - SCOPUS:0034625049

SN - 0027-8424

VL - 97

SP - 5161

EP - 5166

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

IS - 10

ER -