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CrysPINs SIGNED

Crystal structures of PIN proteins - CrysPINs

Total Cost €

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EC-Contrib. €

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Partnership

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Project "CrysPINs" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF WARWICK 

Organization address
address: Kirby Corner Road - University House
city: COVENTRY
postcode: CV4 8UW
website: www.warwick.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-08-01   to  2020-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF WARWICK UK (COVENTRY) coordinator 183˙454.00

Map

 Project objective

The main goal of the “CrysPINS” project is to derive a model for the structure of PIN1 protein, starting with a loopless version (PIN1loopless), and optionally other PIN proteins, using techniques of molecular biology, biochemistry and crystallography. Members of PIN family are plant-specific auxin transporters, which play crucial role in plant morphogenesis, development and responses to the environment. Although it is well known that PIN proteins drive polar auxin transport, till nowadays the auxin research community is missing detailed functional and mechanistic models of these enigmatic transporters. My considerable experience from studying auxin metabolism and transport on the cellular and plant level, combined with the expertise at the University of Warwick in auxin recognition and the structural biology of mammalian membrane transporter proteins, makes it timely to move the science forward by a project focussed on the structure of PINs. My vision is that we will be able to develop a detailed molecular map of PINs together with associated pharmacophoric map for their substrates and inhibitors, a goal that will offer me an ideal system for further research focused on PINs auxin substrate specificity and transport capacity. On the way I will expect to reveal how the PINs are energized, and create links with the auxin herbicide industries to explore opportunities for collaborations on agro-pharmaceutical compound design.

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The information about "CRYSPINS" are provided by the European Opendata Portal: CORDIS opendata.

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