STRUCPER

Structural studies of peroxisomal machinery

 Coordinatore INSTITUTO DE BIOLOGIA MOLECULAR E CELULAR - IBMC 

 Organization address address: RUA DO CAMPO ALEGRE 823
city: PORTO
postcode: 4150 180

contact info
Titolo: Dr.
Nome: Suzana
Cognome: Machado
Email: send email
Telefono: -226074549
Fax: -226067711

 Nazionalità Coordinatore Portugal [PT]
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-IRG-2008
 Funding Scheme MC-IRG
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-09-01   -   2013-08-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    INSTITUTO DE BIOLOGIA MOLECULAR E CELULAR - IBMC

 Organization address address: RUA DO CAMPO ALEGRE 823
city: PORTO
postcode: 4150 180

contact info
Titolo: Dr.
Nome: Suzana
Cognome: Machado
Email: send email
Telefono: -226074549
Fax: -226067711

PT (PORTO) coordinator 100˙000.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

molecular    membrane    components    structures    proteins    import    insertion    organelles    protein   

 Obiettivo del progetto (Objective)

'Peroxisomes are organelles responsible for essential metabolic processes such as fatty acid oxidation. These organelles contain specialized machinery for protein import and membrane protein insertion. These systems have been well characterized at the genetic, cellular and biochemical level and there is a good understanding of the number and identity of the different components and their functional relationships. There is however a lack of structural information about the proteins that are involved in the two machineries, which is reflected in the relatively poor molecular detail of the respective mechanistic models. The general aim of this proposal is the determination of crystal structures of different proteins and protein complexes from the two systems. These structures will reveal molecular details about the different protein components and will provide new insights about the mechanisms of peroxisomal matrix import and membrane protein insertion.'

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