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Pregled bibliografske jedinice broj: 836239

Bacteroides thetaiotaomicron dipeptidyl peptidase III complexes with synthetic substrates


Tomin, Marko; Tomić, Sanja; Sabljić, Igor
Bacteroides thetaiotaomicron dipeptidyl peptidase III complexes with synthetic substrates // ECS3 Book of Abstracts / Jasminka Popović, Aleksandar Višnjevac (ur.).
Zagreb: Croatian Association of Crystallographers, Bijenička 54, HR - 10000 Zagreb, Croatia, VAT: HR47378791658, 2016. str. 14-14 (poster, međunarodna recenzija, sažetak, znanstveni)


Naslov
Bacteroides thetaiotaomicron dipeptidyl peptidase III complexes with synthetic substrates

Autori
Tomin, Marko ; Tomić, Sanja ; Sabljić, Igor

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
ECS3 Book of Abstracts / Jasminka Popović, Aleksandar Višnjevac - Zagreb : Croatian Association of Crystallographers, Bijenička 54, HR - 10000 Zagreb, Croatia, VAT: HR47378791658, 2016, 14-14

Skup
3rd European Crystallography School

Mjesto i datum
Bol, Hrvatska, 25.09.-02.10.2016

Vrsta sudjelovanja
Poster

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
Dipeptidyl peptidase III ; docking ; molecular dynamics ; peptidase

Sažetak
Dipeptidyl peptidase III isolated from Bacteroides thetaiotaomicron is a two-domain zinc exopeptidase from the M49 family. Members of this family, characterized by HEXXGH and EEXR(K)AE(D) motifs, cleave dipeptidyl residues from the N-terminus of their substrates. This conserved region contains two His residues that coordinate the Zn ion along with Glu449 and Glu476. The BtDPP3 crystal structure shows two domains separated by a cleft, strongly resembling the human DPP3 despite the low sequence identity (~23%). In this work we performed docking of synthetic substrates Arg-Arg-2-naphtylamide and Lys-Ala-2-naphtylamide in the wild-type DPPIII and its C450S mutant in order to understand enzyme-ligand interactions. The starting structures were prepared from the human DPPIII-RRNA complex used in previous studies. Complex simulations were performed over the course of 200 ns using ff12sb and ff14sb force fields. These force fields were selected based on their good performance in conformational studies of both human and bacterial DPPIII. Special emphasis has been placed on the zinc ion coordination flexibility, since the existing data for human DPP3 suggests the high plasticity of the Zn2+ coordination. Our results are in qualitative agreement with available kinetic data4 and represent a good starting point for further QM/MM studies necessary to elucidate the mechanism of the bacterial DPPIII.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
HRZZ-IP-2013-11-7235 - Povezanost fleksibilnosti, aktivnosti i strukture u porodici dipeptidil-peptidaza III (Sanja Tomić, )

Ustanove
Institut "Ruđer Bošković", Zagreb