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In both complexes, tetracycline makes significant interactions with the GTPase active site of EF-Tu.



wander
Most of them are involved in stabilizing the structure, particularly loops. The lectin molecule is fairly rigid and does not appear to be affected by changes in temperature.
They are not visible to the user. They are not visible to the user.
Reports on new protein structures are particularly encouraged, as are papers on crystallographic binding studies, structural analysis of mutants and other structure-function studies. Papers on crystallographic methods should be oriented towards biological crystallography, and may include new approaches to any aspect of structure determination or analysis.
BugE has a bound ligand, identified as a glutamate.
The enzyme has two potential N-glycosylation sites.
BugE has a bound ligand, identified as a glutamate.
Some choose to be anonymous.
It adopts the Venus flytrap architecture of periplasmic binding proteins, with two domains separated by a deep cleft.
pertussis BugD, which is an aspartic acid transporter, has recently been reported.
Papers on the crystallization of biological molecules will be accepted providing that these focus on new methods or other features that are of general importance or applicability.
The latter phase requires the identification of the amino-acid side-chain type as well as fitting of the side-chain model into the observed electron density.
A modular and carefully organized suite of programs now handles the whole experimental environment from a single vantage point.
Papers on the crystallization of biological molecules will be accepted providing that these focus on new methods or other features that are of general importance or applicability.
It's fun, easy, inexpensive, and effective at helping students gain familiarity with. Validation of this database on an extensive number of experimental small-molecule crystal structures of varying quality and resolution shows that invariom modelling improves various figures of merit. The algorithm improves on the difficult situations that are commonly observed and poorly handled by the first-generation crystal-centring algorithms. Reports on new protein structures are particularly encouraged, as are papers on crystallographic binding studies, structural analysis of mutants and other structure-function studies.