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Volumn 111, Issue 13, 2007, Pages 3496-3507

Conformational preferences of proline analogues with different ring size

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CHEMICAL BONDS; CHLORINE COMPOUNDS; CONFORMATIONS; ISOMERIZATION; REACTION KINETICS;

EID: 34247483099     PISSN: 15206106     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp066835z     Document Type: Article
Times cited : (28)

References (80)
  • 1
    • 0000218162 scopus 로고
    • Fowden, L. Nature 1955, 176, 347.
    • (1955) Nature , vol.176 , pp. 347
    • Fowden, L.1
  • 49
    • 84906414282 scopus 로고    scopus 로고
    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Zakrzewski, V. G, Montgomery, J. A, Jr, Stratmann, R. E, Burant, J. C, Dapprich, S, Millam, J. M, Daniels, A. D, Kudin, K. N, Strain, M. C, Farkas, O, Tomasi, J, Barone, V, Cossi, M, Cammi, R, Mennucci, B, Pomelli, C, Adamo, C, Clifford, S, Ochterski, J, Petersson, G. A, Ayala, P. Y, Cui, Q, Morokuma, K, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Cioslowski, J, Ortiz, J. V, Baboul, A. G, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Gomperts, R, Martin, R. L, Fox, D. J, Keith, T, Al-Laham, M. A, Peng, C. Y, Nanayakkara, A, Gonzalez, C, Challacombe, M, Gill, P. M. W, Johnson, B, Chen, W, Wong, M. W, Andres, J. L, Gonzalez, C, Head-Gordon, M, Replogle, E. S, Pople, J. A. Gaussian 98, revision A.7; Gaussian, Inc, Pittsburgh, PA, 1998
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Zakrzewski, V. G.; Montgomery, J. A., Jr.; Stratmann, R. E.; Burant, J. C.; Dapprich, S.; Millam, J. M.; Daniels, A. D.; Kudin, K. N.; Strain, M. C.; Farkas, O.; Tomasi, J.; Barone, V.; Cossi, M.; Cammi, R.; Mennucci, B.; Pomelli, C.; Adamo, C.; Clifford, S.; Ochterski, J.; Petersson, G. A.; Ayala, P. Y.; Cui, Q.; Morokuma, K.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Cioslowski, J.; Ortiz, J. V.; Baboul, A. G.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Gomperts, R.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Gonzalez, C.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Andres, J. L.; Gonzalez, C.; Head-Gordon, M.; Replogle, E. S.; Pople, J. A. Gaussian 98, revision A.7; Gaussian, Inc.: Pittsburgh, PA, 1998.
  • 50
    • 84906414283 scopus 로고    scopus 로고
    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery, J. A, Jr, Vreven, T, Kudin, K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Kiene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuraa, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz, J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Martin, R. L, Fox, D. J, Keith, T, Al-L
    • Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery, J. A., Jr.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Kiene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuraa, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz, J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al-Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez, C.; Pople, J. A. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
  • 51
    • 84906399919 scopus 로고    scopus 로고
    • Zimmerman, S. S.; Pottle, M. S.; Nemethy, G.; Scheraga, H. A. Macromolecules 1977, 10, 1. Conformations A, C, and F are defined by the backbone torsion angle V with the backbone torsion angle θ in the range of -110° < θ < -40°: conformation A 1-90° < ψ < -10°; conformation C, 50° < ψ < 130°; conformation F, 130° < ψ < 180° or -180° < ψ < -140°. Conformation D is defined by -180° < 0 < -110° and 20° < ψ < 110°.
    • Zimmerman, S. S.; Pottle, M. S.; Nemethy, G.; Scheraga, H. A. Macromolecules 1977, 10, 1. Conformations A, C, and F are defined by the backbone torsion angle V with the backbone torsion angle θ in the range of -110° < θ < -40°: conformation A 1-90° < ψ < -10°; conformation C, 50° < ψ < 130°; conformation F, 130° < ψ < 180° or -180° < ψ < -140°. Conformation D is defined by -180° < 0 < -110° and 20° < ψ < 110°.
  • 55
    • 84906385690 scopus 로고    scopus 로고
    • CS Chem3D, revision 5.0; CambridgeSoft Co.: Cambridge, MA, 1998.
    • CS Chem3D, revision 5.0; CambridgeSoft Co.: Cambridge, MA, 1998.
  • 56
    • 84906385689 scopus 로고    scopus 로고
    • 57 and pyramidality at prolyl nitrogen for local minima and transition states of Pro, Aze, and Pip dipeptides are discussed in the Supporting Information.
    • 57 and pyramidality at prolyl nitrogen for local minima and transition states of Pro, Aze, and Pip dipeptides are discussed in the Supporting Information.
  • 59
    • 84906399916 scopus 로고    scopus 로고
    • Frisch, A, Frisch, M. J, Trucks, G. W. Gaussian 03 User's Reference, version 7.0; Gaussian, Inc, Pittsburgh, PA, 2003
    • Frisch, A.; Frisch, M. J.; Trucks, G. W. Gaussian 03 User's Reference, version 7.0; Gaussian, Inc.: Pittsburgh, PA, 2003.
  • 61
  • 71
  • 75
    • 0027817195 scopus 로고
    • and references therein
    • Stein, R. L. Adv. Protein Chem. 1993, 44, 1 and references therein.
    • (1993) Adv. Protein Chem , vol.44 , pp. 1
    • Stein, R.L.1
  • 77
    • 84906371568 scopus 로고    scopus 로고
    • It has been reported that the hydrogen bond distance between N-H and O-C of amides increases as the angle α(N-H⋯O) decreases.78 This may imply that the strength of a hydrogen bond becomes weaker as the angle α(N-H⋯O) becomes decreased from its linearity. In particular, the mean value of α(N-H⋯O) is appreciably smaller for the intramolecular hydrogen bonds (132.5°±15°) than for the intermolecular hydrogen bonds (161.2°±3°).78 However, the distance between the proton and its acceptor has been widely chosen as a criterion of hydrogen bonding.79 Although the angle α(N-H⋯N) for the transition states of Aze, Pro, and Pip dipeptides is calculated to be ∼108°, the distance r(H⋯N) is in the range of 2.25 Å to 2.32 Å, which can be classified as a weak hydrogen bond.79
    • 79


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