1TMH

MODULAR MUTAGENESIS OF A TIM-BARREL ENZYME: THE CRYSTAL STRUCTURE OF A CHIMERIC E. COLI TIM HAVING THE EIGHTH (BETA-ALPHA)-UNIT REPLACED BY THE EQUIVALENT UNIT OF CHICKEN TIM

1TMH の概要

• エントリーDOI: 10.2210/pdb1tmh/pdb
• 分子名称: TRIOSEPHOSPHATE ISOMERASE, SULFATE ION (2 entities in total)
• 機能のキーワード: isomerase(intramolecular oxidoreductase)
• 由来する生物種: Escherichia coli
• 細胞内の位置: Cytoplasm (Probable): P0A858
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 108859.64

構造登録者

Radha Kishan, K.V.,Zeelen, J.Ph.,Wierenga, R.K. (登録日: 1994-03-22, 公開日: 1994-06-22, 最終更新日: 2024-02-14)

主引用文献

Kishan, R.,Zeelen, J.P.,Noble, M.E.,Borchert, T.V.,Mainfroid, V.,Goraj, K.,Martial, J.A.,Wierenga, R.K.
Modular mutagenesis of a TIM-barrel enzyme: the crystal structure of a chimeric E. coli TIM having the eighth beta alpha-unit replaced by the equivalent unit of chicken TIM.
Protein Eng., 7:945-951, 1994

PubMed Abstract: The crystal structure of a hybrid Escherichia coli triosephosphate isomerase (TIM) has been determined at 2.8 A resolution. The hybrid TIM (ETIM8CHI) was constructed by replacing the eighth beta alpha-unit of E. coli TIM with the equivalent unit of chicken TIM. This replacement involves 10 sequence changes. One of the changes concerns the mutation of a buried alanine (Ala232 in strand 8) into a phenylalanine. The ETIM8CHI structure shows that the A232F sequence change can be incorporated by a side-chain rotation of Phe224 (in helix 7). No cavities or strained dihedrals are observed in ETIM8CHI in the region near position 232, which is in agreement with the observation that ETIM8CHI and E.coli TIM have similar stabilities. The largest CA (C-alpha atom) movements, approximately 3 A, are seen for the C-terminal end of helix 8 (associated with the outward rotation of Phe224) and for the residues in the loop after helix 1 (associated with sequence changes in helix 8). From the structure it is not clear why the kcat of ETIM8CHI is 10 times lower than in wild type E.coli TIM.

PubMed: 7809033
DOI: 10.1093/protein/7.8.945

実験手法

X-RAY DIFFRACTION (2.8 Å)