Side-Chains Configurations in Coiled Coils Revealed by the 5.15-Å Meridional Reflection on Hard α-Keratin X-Ray Diffraction Patterns - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Structural Biology Année : 1999

Side-Chains Configurations in Coiled Coils Revealed by the 5.15-Å Meridional Reflection on Hard α-Keratin X-Ray Diffraction Patterns

Résumé

The origin of the 5.15-Å meridional reflection on hard-keratin X-ray diffraction patterns is discussed in terms of side-chains conformations. We show it to reveal specific configurations of the side chains which are common to all two-stranded-heli-cal coiled coils. Combining literature data on cryst-allised coiled coil pieces and molecular dynamics results with our X-ray diffraction pattern simulations , we propose rules for the attribution of 1 torsion angles for coiled coils involved in fibres whose structure cannot be resolved at atomic resolution: in a (a b c d e f g) heptad repeat, a and d residues, respectively, adopt mean t and g configurations , whereas statistical rules are given for the other residues. 1999 Academic Press

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hal-02111152 , version 1 (13-05-2019)

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Bertrand Busson, Fatma Briki, Jean Doucet. Side-Chains Configurations in Coiled Coils Revealed by the 5.15-Å Meridional Reflection on Hard α-Keratin X-Ray Diffraction Patterns. Journal of Structural Biology, 1999, 125 (1), pp.1-10. ⟨10.1006/jsbi.1999.4082⟩. ⟨hal-02111152⟩
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