1OAD

Glucose isomerase from Streptomyces rubiginosus in P21212 crystal form

1OAD の概要

• エントリーDOI: 10.2210/pdb1oad/pdb
• 関連するPDBエントリー: 1GW9 1MNZ 1O1H 1XIB 1XIC 1XID 1XIE 1XIF 1XIG 1XIH 1XII 1XIJ 1XIS 2XIS 3XIS 4XIS 8XIA 9XIA
• 分子名称: XYLOSE ISOMERASE, MANGANESE (II) ION, MAGNESIUM ION, ... (8 entities in total)
• 機能のキーワード: isomerase, glucose isomerase, xylose isomerase
• 由来する生物種: STREPTOMYCES RUBIGINOSUS
• 細胞内の位置: Cytoplasm: P24300
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 87472.07

構造登録者

Ramagopal, U.A.,Dauter, M.,Dauter, Z. (登録日: 2003-01-08, 公開日: 2003-01-30, 最終更新日: 2024-05-08)

主引用文献

Ramagopal, U.A.,Dauter, M.,Dauter, Z.
Sad Manganese in Two Crystal Forms of Glucose Isomerase
Acta Crystallogr.,Sect.D, 59:868-, 2003

PubMed Abstract: Glucose isomerase from Streptomyces rubiginosus was crystallized in two forms: I222, with one molecule of 44 kDa in the asymmetric unit, and P2(1)2(1)2, with two unique molecules. The I222 structure is known, but the P2(1)2(1)2 form has not been solved before. X-ray diffraction data for the P2(1)2(1)2 form were collected at a wavelength of 1.54 A and data for the I222 form were collected at three different wavelengths: 1.34, 1.07 and 0.98 A. The amount of anomalous signal from one Mn and eight S atoms in these data sets varies from 1.24% to as low as 0.56%. The dual-space direct-methods program SHELXD, run against the Bijvoet differences, gave a clear solution of all anomalous scatterers for all data sets. The Mn positions only were used for SAD phasing of all four data sets. The electron-density map after density modification, resulting from the phasing of a single-wavelength data set and based purely on the anomalous deltaf" contribution, was clearly interpretable; an almost complete model of the protein was built by wARP without human intervention in all four cases. As far as is known, this is the first time that an anomalous signal as low as 0.6% has successfully been used to determine the structure of a macromolecule.

PubMed: 12777803
DOI: 10.1107/S0907444903005663

実験手法

X-RAY DIFFRACTION (1.5 Å)