Pregled bibliografske jedinice broj: 1153550
Adenylosuccinate Synthetase from Helicobacter pylori: Characterization of Active Site Using X- ray Diffraction and Molecular Dynamics Simulations
Adenylosuccinate Synthetase from Helicobacter pylori: Characterization of Active Site Using X- ray Diffraction and Molecular Dynamics Simulations // 27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts / Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2021. str. 194-194 (poster, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 1153550 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Adenylosuccinate Synthetase from Helicobacter
pylori: Characterization of Active Site Using X-
ray Diffraction and Molecular Dynamics Simulations
Autori
Bubić, Ante ; Štefanić, Zoran ; Bertoša, Branimir ; Leščić Ašler, Ivana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts
/ Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna - Zagreb : Hrvatsko kemijsko društvo, 2021, 194-194
Skup
27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI)
Mjesto i datum
Veli Lošinj, Hrvatska, 05.10.2021. - 08.10.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
Helicobacter pylori ; adenylosuccinate synthetase ; enzyme active site ; X-ray structure ; molecular dynamics simulations
Sažetak
Helicobacter pylori is pathogenic bacterium which colonizes the gastric epithelia.[1] It is categorized as number one carcinogen inducer for gastric carcinoma.[2] Since H. pylori lacks the genes for de novo synthesis of purines, to maintain its viability, the pathogen uses purines from recycling pathway.[3] Adenylosuccinate synthetase (AdSS) is an essential enzyme in the purine synthesis and it operates in both purine de novo synthesis and purine recycling pathway. AdSS utilizes L-aspartate and IMP along with GTP and magnesium ions to form S-AMP which can be converted into AMP by adenylosuccinate lyase in the further step. As one of the steps on the path to decipher and describe the catalytic mechanism of this enzyme, we obtained the crystals and solved the structure of AdSS complexed with substrates (IMP and GTP-Mg) and inhibitor hadacidin. Analysis of the active site showed the presence of stable intermediate 6’-phosphoryl-IMP. Molecular dynamics’ simulations showed differences in conformation of the GTP binding loop depending on the presence of IMP in the active site. [1] S. Nishiumi, M. Yoshida, T. Azuma, Microb. Pathog. 2017, 109, 78–85. [2] U: IARC Monogr. Eval. Carcinog. Risks Hum.: 1994. [3] K. M. Sanders, T. A. Stern, P. T. O’gara, T. S. Field, S. L. Rauch, R. E. Lipson, K. A. Eagle, Psychosomatics 1992, 33, 35–44.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Projekti:
IP-2013-11-7423 - Enzimi purinskog reciklirajućeg ciklusa iz Helicobacter pylori i Escherichie coli (PSPE) (Luić, Marija, HRZZ - 2013-11) ( CroRIS)
HRZZ-IP-2019-04-6764 - Alosterički komunikacijski putevi u oligomernim enzimima (ALOKOMP/ALOCOMP) (Štefanić, Zoran, HRZZ - 2019-04) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Branimir Bertoša (autor)
Ante Bubić (autor)
Ivana Leščić Ašler (autor)
Zoran Štefanić (autor)