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Promiscuous scaffolds in proteins - non-native, non-additive and non-trivial

Promiscuous scaffolds in proteins - non-native, non-additive and non-trivial


Title: Promiscuous scaffolds in proteins - non-native, non-additive and non-trivial
Author: Chakraborty, Sandeep
Ásgeirsson, Bjarni   orcid.org/0000-0002-4275-2732
Dutta, Mouparna
Ghosh, Anindya S.
Oda, Masataka
Rendón, Adela
Goñi, Felix
Frere, Jean-Marie
Venkatramani, Ravindra
Dandekar, Abhaya M.
... 1 more authors Show all authors
Date: 2014-01-20
Language: English
University/Institute: Háskóli Íslands
University of Iceland
School: Verkfræði- og náttúruvísindasvið (HÍ)
School of Engineering and Natural Sciences (UI)
Department: Raunvísindadeild (HÍ)
Faculty of Physical Sciences (UI)
Raunvísindastofnun (HÍ)
Science Institute (UI)
Series: F1000Research;2(260)
ISSN: 2046-1402
DOI: 10.12688/f1000research.2-260.v2
URI: https://hdl.handle.net/20.500.11815/2016

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Citation:

Chakraborty S, Asgeirsson B, Dutta M et al. Promiscuous scaffolds in proteins - non-native, non-additive and non-trivial [version 2; peer review: 1 approved with reservations, 2 not approved]. F1000Research 2014, 2:260 (https://doi.org/10.12688/f1000research.2-260.v2)

Abstract:

Promiscuity, the ability of an enzyme to catalyze diverse activities using the same active site, sets up the stage for the evolution of complex organisms through gene duplication and specialization. The detection of promiscuous motifs is crucial to understand the physiological relevance of a protein, or for any endeavor that intends to rationally modify these latent capabilities to design new proteins under laboratory conditions. We have established a methodology for identifying catalytic residues based on spatial and electrostatic congruence with known active site configurations. Here, we discuss insights gained in several initiatives using our method on different enzymes.

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Rights:

© 2014 Chakraborty S et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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