CRYSTAL STRUCTURE OF CATALYTIC CORE FRAGMENT OF ROUS SARCOMA VIRUS INTEGRASE

我们收集了植酸酶的数据(1483个氨基酸残基)。在……里面 自闭症。单位，大麦天冬氨酸蛋白酶)在2.3A分辨率下， 10-甲酰基四氢叶酸酶(FDH)的N-末端结构域，(620 瑞斯。用阿西姆语。单位)在3.0A重新解决和N端子上的MAD数据 STAT4的结构域(496分辨率用阿西姆语。通过使用这些数据，我们 解决了植酸酶的结构，现在最终的提纯工作在 进步。外佣的结构还没有解决。STAT4 MAD数据 事实证明这是没有用的，因为斐氏轴线下滑到了2度。在.期间 在我们使用光束反转的同时进行数据收集。问题在于 斐氏斧头已经报告给国际象棋工程师了，据我所知，现在 它已经修好了。

We have collected data on phytepsin (1483 amino acid res. in assym. unit, barley aspartic protease) at 2.3 A resolution, N-terminal domain of 10-formyltetrahydrofolate enzyme (FDH), ( 620 res. in assym. unit) at 3.0 A re-solution and MAD data on N-terminal domain of STAT4 (496 res. in assym. unit) By using these data we solved structure of phytepsin and now the final refine-ment is in progress. FDH structure has not been solved yet. STAT4 MAD data proved to be useless, since Phi axes was slipping up to 2 deg. during data collection while we were using beam inversion. The problem with the Phi axes had been reported to CHESS engineers, and as I know, now it has been fixed.