Abstract

The atomic displacements of many of the atoms in a macromolecular structure can be modelled in terms of group motions described in the harmonic approximation by T, L and S tensors. Relevant groups may be planar side groups of protein chains, units of secondary structure such as α-helices or whole protein domains. For the TLS parameters to be interpreted, they must be related to the axes of inertia of the rigid groups and, in the case of the T and S tensors, must be calculated with respect to the centre of reaction of the rigid group. A program (TLSANL) is described that analyses these 21 TLS rigid-body displacement parameters and their relation with the principal axes of the rigid body, from the output of the segmented anisotropic refinement of a macromolecular structure, as produced by a program such as RESTRAIN [Haneef, Moss, Stanford & Borkakoti (1985). Acta Cryst. A41, 426–433; Driessen, Haneef, Harris, Howlin, Khan & Moss (1989). J. Appl. Cryst. 22, 510–516].

Keywords

MacromoleculeAnisotropyRigid bodyPlanarDisplacement (psychology)Principal axis theoremGroup (periodic table)CrystallographyMaterials sciencePhysicsChemistryGeometryClassical mechanicsMathematicsComputer scienceOpticsQuantum mechanics

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Publication Info

Year
1993
Type
article
Volume
26
Issue
4
Pages
622-624
Citations
103
Access
Closed

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Brendan J. Howlin, S. A. Butler, D. S. Moss et al. (1993). <i>TLSANL</i>: TLS parameter-analysis program for segmented anisotropic refinement of macromolecular structures. Journal of Applied Crystallography , 26 (4) , 622-624. https://doi.org/10.1107/s0021889893002729

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DOI
10.1107/s0021889893002729