## Abstract The program Generate, aimed at generating 3‐D structures for peptides and peptidomimetics, is presented. The algorithm is based on a build‐up procedure, using a library of conformations of amino acid residues. This library is built from conformational analysis of amino acids placed in a
Generic shapes for the conformation analysis of macrocyclic structures
✍ Scribed by Paul R. Gerber; Klaus Gubernator; Klaus Müller
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- German
- Weight
- 895 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
~~ ~~~
A new algorithm for the systematic generation of conformations of macrocyclic systems is presented. The procedure is based on the concept of generic shapes that are found in such structures. These shapes are characterized by a selection of harmonics which occur in an approximate Fourier representation of the atomic coordinates of the rings. Following a fixed protocol, a limited set of in-plane and out-of-plane circular harmonics is used to define an ensemble of generic ring shapes. These generic shapes are used as start structures for energy minimizations by a given force-field method. To account for the possibility of having several final conformations originating from the same generic shape, the corresponding initial structure is taken several times and subjected to a randomization step before minimization. The resulting conformations that fall within a preset low-energy band are collected and screened for duplicates and enantiomers. The efficiency of this procedure (ratio between the number of accepted conformations and the total number of energy minimizations) depends on the flexibility of the macrocyclic system. The efficiency is generally quite high for very flexible rings. According to the proposed protocol, the number of generic shapes used as start structures grows as the square of N(lnN), where Nis the ring size. The algorithm lends itself to conformational analyses of medium-size and large rings as well as of loops spanned between fixed structural units.
📜 SIMILAR VOLUMES
## Abstract The parameters for the OPLS–AA potential energy function have been extended to include some functional groups that are present in macrocyclic polyketides. Existing OPLS–AA torsional parameters for alkanes, alcohols, ethers, hemiacetals, esters, and ketoamides were improved based on MP2/
## Abstract A small number of macrocyclic dilactones of type **3**, __i.e.__, **9, 10, 11**, and epi‐**11**, comprising a 3,4‐dihydroxypentanoic acid unit, the pharmacophore of aplysiatoxin, and a conformationally preorganized __ω__‐hydroxynonanoic acid unit were synthesized. Conformational analysi
It has been about 25 years since Staab prepared a hexameric phenyl-ethynyl macrocycle by the statistical cyclization of the copper salt of m-iodo-phenylacetylene in 4.6% yield. Since that time, different methodologies have been investigated that allow not only the preparation of selec-tively functio
An updated Lagrangian formulation of the generalized conforming ¯at shell element with drilling degrees of freedom is derived based on the incremental equation of virtual work of a three-dimensional (3D) continuum for a purely geometric non-linear analysis of the space structure. While solving the n