1TCD

TRYPANOSOMA CRUZI TRIOSEPHOSPHATE ISOMERASE

1TCD の概要

• エントリーDOI: 10.2210/pdb1tcd/pdb
• 分子名称: TRIOSEPHOSPHATE ISOMERASE (2 entities in total)
• 機能のキーワード: isomerase, intramolecular oxidoreductase, glycolysis, isomerization between glyceraldehyde 3-phosphate and dihydroxyacetone, alpha-beta barrel
• 由来する生物種: Trypanosoma cruzi
• 細胞内の位置: Glycosome: P52270
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 54316.33

構造登録者

Maldonado, E.,Soriano-Garcia, M.,Cabrera, N.,Garza-Ramos, G.,Tuena De Gomez-Puyou, M.,Gomez-Puyou, A.,Perez-Montfort, R. (登録日: 1998-01-29, 公開日: 1999-01-13, 最終更新日: 2024-05-22)

主引用文献

Maldonado, E.,Soriano-Garcia, M.,Moreno, A.,Cabrera, N.,Garza-Ramos, G.,de Gomez-Puyou, M.,Gomez-Puyou, A.,Perez-Montfort, R.
Differences in the intersubunit contacts in triosephosphate isomerase from two closely related pathogenic trypanosomes.
J.Mol.Biol., 283:193-203, 1998

PubMed Abstract: The aligned amino acid sequences of TIM from Trypanosoma cruzi (TcTIM) and Trypanosoma brucei (TbTIM) have a positional identity of 68%. The two enzymes have markedly similar catalytic properties. Agents that interact with their interface Cys inhibit TcTIM and TbTIM; and those TIMs that lack this Cys (such as human TIM) are largely or completely insensitive to these agents. The susceptibility of TcTIM to the agents is approximately 100 times higher than that of TbTIM. To ascertain the cause of this large difference, the crystal structure of TcTIM was solved at 1.83 A resolution. The two enzymes are very similar homodimers. In TcTIM and TbTIM their respective Cys, 15 or 14, forms part of the dimer interface. In both, the contacts of the Cys with residues of the other subunit are almost identical. Nevertheless, there are noteworthy differences between the two; the existence of glutamine 18 in TbTIM instead of glutamic acid in TcTIM at the beginning of helix 1 decreases the contacts between this portion of the protein and helix 3 of the other subunit. In addition, TcTIM has proline at position 24 in the first helix of the TIM barrel; this is absent in the other TIM. Pro24 disrupts the regular helix arrangement, making the pitch of this helix 1.2 A longer than in TbTIM. When Pro24 of TcTIM was substituted for Glu, the sensitivity of TcTIM to sulfhydryl reagents increased about fivefold, possibly as a consequence of an increase in the space between the first portion of helix 1 and helix 3 of the other subunit. Therefore, it may be concluded that the geometry of the latter region is central in the accessibility to agents that perturb the interface Cys. In human TIM this region is more compact.

PubMed: 9761683
DOI: 10.1006/jmbi.1998.2094

実験手法

X-RAY DIFFRACTION (1.83 Å)