a measure of the promiscuity of proteins and characteristics of residues in the vicinity of the catalytic site that regulate promiscuity蛋白质的滥交和附近的残留特征调节滥交的催化部位.pdfVIP
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a measure of the promiscuity of proteins and characteristics of residues in the vicinity of the catalytic site that regulate promiscuity蛋白质的滥交和附近的残留特征调节滥交的催化部位
A Measure of the Promiscuity of Proteins and
Characteristics of Residues in the Vicinity of the Catalytic
Site That Regulate Promiscuity
Sandeep Chakraborty, Basuthkar J. Rao*
Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India,
Abstract
Promiscuity, the basis for the evolution of new functions through ‘tinkering’ of residues in the vicinity of the catalytic site, is
yet to be quantitatively defined. We present a computational method Promiscuity Indices Estimator (PROMISE) - based on
signatures derived from the spatial and electrostatic properties of the catalytic residues, to estimate the promiscuity
(PromIndex) of proteins with known active site residues and 3D structure. PromIndex reflects the number of different active
site signatures that have congruent matches in close proximity of its native catalytic site, the quality of the matches and
difference in the enzymatic activity. Promiscuity in proteins is observed to follow a lognormal distribution (m = 0.28, s = 1.1
reduced chi-square = 3.0E-5). The PROMISE predicted promiscuous functions in any protein can serve as the starting point
for directed evolution experiments. PROMISE ranks carboxypeptidase A and ribonuclease A amongst the more promiscuous
proteins. We have also investigated the properties of the residues in the vicinity of the catalytic site that regulates its
promiscuity. Linear regression establishes a weak correlation (R2 ,0.1) between certain properties of the residues (charge,
polar, etc) in the neighborhood of the catalytic residues and PromIndex. A stronger relationship states that most proteins
˚
with high pro
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