6X44

High Resolution Crystal Structure Analysis of SERA5 proenzyme from plasmodium falciparum

6X44 の概要

• エントリーDOI: 10.2210/pdb6x44/pdb
• 分子名称: Serine repeat antigen 5, DI(HYDROXYETHYL)ETHER (3 entities in total)
• 機能のキーワード: malaria, prodomain, protease, hydrolase
• 由来する生物種: Plasmodium falciparum
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 101802.78

構造登録者

Clarke, O.B.,Smith, N.A.,Lee, M.,Smith, B.J. (登録日: 2020-05-22, 公開日: 2020-10-07, 最終更新日: 2024-11-13)

主引用文献

Smith, N.A.,Clarke, O.B.,Lee, M.,Hodder, A.N.,Smith, B.J.
Structure of the Plasmodium falciparum PfSERA5 pseudo-zymogen.
Protein Sci., 29:2245-2258, 2020

PubMed Abstract: PfSERA5, a significantly abundant protein present within the parasitophorous vacuole (PV) and essential for normal growth during the blood-stage life cycle of the malaria parasite Plasmodium falciparum, displays structural similarity to many other cysteine proteases. However, PfSERA5 does not exhibit any detectable protease activity and therefore the role of the PfSERA5 papain-like domain (PfSERA5E), thought to remain bound to its cognate prodomain, remains unknown. In this study, we present a revised structure of the central PfSERA5E domain at a resolution of 1.2 Å, and the first structure of the "zymogen" of this papain-like domain including its cognate prodomain (PfSERA5PE) to 2.2 Å resolution. PfSERA5PE is somewhat structurally similar to that of other known proenzymes, retaining the conserved overall folding and orientation of the prodomain through, and occluding, the archetypal papain-like catalytic triad "active-site" cleft, in the same reverse direction as conventional prodomains. Our findings are congruent with previously identified structures of PfSERA5E and of similar "zymogens" and provide a foundation for further investigation into the function of PfSERA5.

PubMed: 32955133
DOI: 10.1002/pro.3956

実験手法

X-RAY DIFFRACTION (2.19733954166 Å)