𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Side-chain conformation angles of amino acids: effect of temperature factor cut-off

✍ Scribed by G Ramya Bhargavi; S.S Sheik; D Velmurugan; K Sekar


Book ID
116696518
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
171 KB
Volume
143
Category
Article
ISSN
1047-8477

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Modeling of the Amino Acid Side Chain Ef
✍ Katrin Sak; Mati Karelson; Jaak JΓ€rv πŸ“‚ Article πŸ“… 1999 πŸ› Elsevier Science 🌐 English βš– 76 KB

Semiempirical AM1 calculations were carried out for quantum-chemically optimized minimum energy conformations of peptides (Ala) 4 -X-(Ala) 4 , where X stands for different L-␣amino acids (Ala,

Conformational constraints of amino acid
✍ Lucjan Piela; George Nemethy; Harold A. Scheraga πŸ“‚ Article πŸ“… 1987 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 678 KB

The conformational freedom of amino acid side chains is strongly reduced when the side chains occur on an a-helix. A quantitative evaluation of this freedom has been carried out by means of conformational energy computations for all naturally occurring amino acids and for a-aminobutyric acid when th

Backbone and side-chain conformations of
✍ V. Sasisekharan; P. K. Ponnuswamy πŸ“‚ Article πŸ“… 1970 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 198 KB πŸ‘ 2 views

Although the conformations of two linked peptide units both with glycyl and alanyl residues have been extensively studied,'-$ no systematic investigation of the energies of conformations of two linked peptide units with side chains beyond the CB atom and a comparison with the available crystallograp

Design of serine protease inhibitors wit
✍ Yasuyuki Shimohigashi; Takeru Nose; Yasuko Yamauchi; Iori Maeda πŸ“‚ Article πŸ“… 1999 πŸ› Wiley (John Wiley & Sons) 🌐 English βš– 232 KB πŸ‘ 1 views

A novel type of conformationally restricted peptides with the structure of H-D-Xaa-Phe-NH-CH 2 -C 6 H 5 has been developed as inhibitors of serine proteinase chymotrypsin. The D-Xaa-alkyl and Phe-phenyl groups resulted in a formation of the hydrophobic core due to the side-chain-side-chain CH/ inter