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  1. 研究論文

Two alternative conformational states of α,α-dialkylglycyl-L- prolyl sequences governed by presence/absence of an NH group directly following the proline residue. X-ray crystal and molecular structures of Boc-D-Iva-L-Pro-NHBzl and Boc-L-Iva-L-Pro-NHBzl

https://nitech.repo.nii.ac.jp/records/4316
https://nitech.repo.nii.ac.jp/records/4316
f97584a1-53e3-44c6-9d5d-a835c0b70643
名前 / ファイル ライセンス アクション
JCSP 本文_fulltext (1.0 MB)
J. CHEM. SOC. PERKIN TRANS. I 1995, 2215-2122 - Reproduced by permission of The Royal Society of Chemistry (RSC)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2012-11-06
タイトル
タイトル Two alternative conformational states of α,α-dialkylglycyl-L- prolyl sequences governed by presence/absence of an NH group directly following the proline residue. X-ray crystal and molecular structures of Boc-D-Iva-L-Pro-NHBzl and Boc-L-Iva-L-Pro-NHBzl
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Kawai, Masao

× Kawai, Masao

en Kawai, Masao

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Omori, Yoshimasa

× Omori, Yoshimasa

en Omori, Yoshimasa

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Yamamura, Hatsuo

× Yamamura, Hatsuo

en Yamamura, Hatsuo

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Butsugan, Yasuo

× Butsugan, Yasuo

en Butsugan, Yasuo

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Taga, Toru

× Taga, Toru

en Taga, Toru

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Miwa, Yoshihisa

× Miwa, Yoshihisa

en Miwa, Yoshihisa

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著者別名
姓名 山村, 初雄
書誌情報 en : Journal of the Chemical Society. Perkin transactions 1

巻 1995, 号 17, p. 2115-2122, 発行日 1995-01-01
出版者
出版者 Royal Society of Chemistry
言語 en
ISSN
収録物識別子タイプ ISSN
収録物識別子 0300-922X
item_10001_source_id_32
収録物識別子タイプ NCID
収録物識別子 AA00695134
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
item_10001_relation_34
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1039/P19950002115
関連名称 10.1039/P19950002115
内容記述
内容記述タイプ Other
内容記述 The crystal structures of the isovaline-containing dipeptides, Boc-D-Iva-L-Pro-NHBzl 4 and Boc-L-Iva-L-Pro-NHBzl 5 were determined by X-ray diffraction. The diastereoisomeric peptides adopt intramolecular hydrogen-bonded β-turn conformations closely similar to each other (4:φIva-51°, ψIva-38°, φPro-70° and ψPro-17° and 5: φIva-53°, ψIva-35°, φPro-72° and ψPro-14°). The Pro ring of each peptide is in Cγ-exo conformation. These conformations are essentially the same as those in the reported crystal structures of the Aib-L-Pro sequence possessing an NH group directly attached to the carbonyl of the L-Pro, indicating that replacement of either one of the two methyl groups of the Aib moiety with an ethyl group does not cause any significant change in the β-turn conformation of the Aib-L-Pro sequence in the crystalline state.CD spectral analysis of the terminal chromophoric group-carrying peptides Dnp-Gly-X-L-Pro-Gly-pNA (X = Aib 6 and D/L-Iva 7/8) has shown that these three tetrapeptides in CHCl3 and THF solutions also adopt a β-turn-type conformation. CD spectra of glycolic acid residue-containing analogues in place of the fourth Gly residue revealed a lack of β-turn tendency in these analogues, indicating the importance of intramolecular hydrogen bonding for the β-turn conformation of the central dipeptide moieties. The results are consistent with the reported unturned crystal structures of Aib-L-Pro arid D/L-Iva-L-Pro sequence-containing peptides lacking the NH group which directly follows the Pro residue available for intramolecular hydrogen bonding.
言語 en
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