Výsledky vyhledávání - "T A, Makhmudova"

Spatial Structure of BAM-12P Dodecapeptide and Its Analogues

Autor: N.A. Akhmedov, Z. H. Tagiev, T. A. Makhmudova, E. M. Hasanov

Publikováno v: Russian Journal of Bioorganic Chemistry. 31:216-220

Theoretical conformational analysis was used to study the spatial structure and conformational properties of the bovine adrenal medulla dodecapeptide BAM-12P (Tyr1-Gly2-Gly3-Phe4-Met5-Arg6-Arg7-Val8-Gly9-Arg10-Pro11-Glu12). Twenty-three low-energy co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d39cf6b127b670a24da2a96f03b2b48
https://doi.org/10.1007/s11171-005-0030-8

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[Structural organization of rimorphin and its synthetic analogs]

Autor: N A, Akhmedov, T A, Makhmudova, R I, Khalilov, N M, Zeĭnalova

Publikováno v: Bioorganicheskaia khimiia. 21(8)

The spatial structure and conformations of rimorphin were investigated using theoretical conformational analysis. The spatial organization of the peptide can be described by a set of 11 low-energy conformations of the backbone. By solving the reverse

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::34483c72073a7a23a6dff05404f95fb0
https://pubmed.ncbi.nlm.nih.gov/8540899

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[Approach to the study of natural peptides from structure to functions. III. Structural organization of an adrenorphin molecule and its synthetic analogs]

Autor: N A, Akhmedov, T A, Makhmudova, E M, Popov

Publikováno v: Bioorganicheskaia khimiia. 19(6)

Spatial structure of the peptide hormone adrenorphin was investigated by the theoretical conformational method. A solution of the "reverse conformational problem" for adrenorphin made it possible to predict a series of the modified synthetic analogue

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9169aa0dab7338736a45915b1119202b
https://pubmed.ncbi.nlm.nih.gov/8363653

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[Approach to studying the structure-activity relationship of native peptides. I. Structural organization of the opioid peptide Tyr-Glu-Gly-Phe-Met-Arg-Gly-Leu and its artificial analogs]

Autor: E M, Popov, N A, Akhmedov, T A, Makhmudova

Publikováno v: Bioorganicheskaia khimiia. 18(12)

Theoretical conformational analysis was carried out for the octapeptide Tyr1-Gly2-Gly3-Phe4-Met5-Arg6-Gly7-Leu8. Possible structure of the opioid peptide under physiological conditions may be described by a set of low-energy conformations belonging t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::27853b88e9440d70af00a63d36413ae4
https://pubmed.ncbi.nlm.nih.gov/1300997

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