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Presence of pseudo-peptide bond in the crystal structure of n-(t-butoxycarbonyl)-ε-n′-benzyloxycarbony-l-lysyl-l-isoleucine (boc-lys(obzl)-ile)
The dipeptide Boc‐Lys(OBzl)‐Ile crystallizes in monoclinic space group P21 with cell parameters a = 5.003(1), b = 19.199(3), c = 15.270(2)Å, β =93.42(1)°, V = 1464.1(3)Å3, Z = 2, Dcal = 1.117 Mg/m3 at T = 293 K. The structure was solved by direct methods and refined by full‐matrix least‐squares proc...
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Published in: | Crystal research and technology (1979) 2004-04, Vol.39 (4), p.368-374 |
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container_end_page | 374 |
container_issue | 4 |
container_start_page | 368 |
container_title | Crystal research and technology (1979) |
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creator | Malathy Sony, S. M. Sukumar, N. Ponnuswamy, M. N. Jayakumar, R. |
description | The dipeptide Boc‐Lys(OBzl)‐Ile crystallizes in monoclinic space group P21 with cell parameters a = 5.003(1), b = 19.199(3), c = 15.270(2)Å, β =93.42(1)°, V = 1464.1(3)Å3, Z = 2, Dcal = 1.117 Mg/m3 at T = 293 K. The structure was solved by direct methods and refined by full‐matrix least‐squares procedure to a final R = 0.096 and wR = 0.101 using 1379 reflections. The peptide unit is in trans conformation and the molecule takes up an extended conformation. In the lysine side chain, delocalization of electrons and pseudo peptide bond formation is observed at the interaction site of benzyloxycarbonyl group. Both N‐H…O and main chain C‐H…O hydrogen bonds stabilize the molecules in the unit cell in a parallel β‐sheet fashion. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) |
doi_str_mv | 10.1002/crat.200310197 |
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M. ; Sukumar, N. ; Ponnuswamy, M. N. ; Jayakumar, R.</creator><creatorcontrib>Malathy Sony, S. M. ; Sukumar, N. ; Ponnuswamy, M. N. ; Jayakumar, R.</creatorcontrib><description>The dipeptide Boc‐Lys(OBzl)‐Ile crystallizes in monoclinic space group P21 with cell parameters a = 5.003(1), b = 19.199(3), c = 15.270(2)Å, β =93.42(1)°, V = 1464.1(3)Å3, Z = 2, Dcal = 1.117 Mg/m3 at T = 293 K. The structure was solved by direct methods and refined by full‐matrix least‐squares procedure to a final R = 0.096 and wR = 0.101 using 1379 reflections. The peptide unit is in trans conformation and the molecule takes up an extended conformation. In the lysine side chain, delocalization of electrons and pseudo peptide bond formation is observed at the interaction site of benzyloxycarbonyl group. Both N‐H…O and main chain C‐H…O hydrogen bonds stabilize the molecules in the unit cell in a parallel β‐sheet fashion. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)</description><identifier>ISSN: 0232-1300</identifier><identifier>EISSN: 1521-4079</identifier><identifier>DOI: 10.1002/crat.200310197</identifier><language>eng</language><publisher>Berlin: WILEY-VCH Verlag</publisher><subject>crystal ; dipeptide ; hydrogen bonds ; isoleucine ; lysine ; pseudo peptide bond</subject><ispartof>Crystal research and technology (1979), 2004-04, Vol.39 (4), p.368-374</ispartof><rights>Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2807-55995b5826a09e1cdc68687e3091d26abe8606e1f75bb2d3176cdf55c6fe9c013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Malathy Sony, S. 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In the lysine side chain, delocalization of electrons and pseudo peptide bond formation is observed at the interaction site of benzyloxycarbonyl group. Both N‐H…O and main chain C‐H…O hydrogen bonds stabilize the molecules in the unit cell in a parallel β‐sheet fashion. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)</description><subject>crystal</subject><subject>dipeptide</subject><subject>hydrogen bonds</subject><subject>isoleucine</subject><subject>lysine</subject><subject>pseudo peptide bond</subject><issn>0232-1300</issn><issn>1521-4079</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkM1KxDAUhYMoOP5sXXc5LjLepCZtljL4h7-IorgJTXqL1doOSYrWlc_gowi-hg_hk9hxRN25uRfOPd_lcAhZYzBiAHzDuiyMOEDMgKlkjgyY4IxuQqLmyQB4zCmLARbJkve3AKDkJh-Ql1OHHmuLUVNEE49t3tAJTkKZY2SaOo_KOgo3GFnX-ZBVkQ-utaF1X_6aDgM1bWgeO5u53t5V6_T9jdYfz6_UYP3UVb8nWtGq810_aembCltb1hgNTWOn-rAxTz1cVri-QhaKrPK4-r2XycXO9vl4jx6e7O6Ptw6p5SkkVAilhBEplxkoZDa3MpVpgjEolveiwVSCRFYkwhiexyyRNi-EsLJAZYHFy2Q0-2td473DQk9ceZ-5TjPQ00b1tFH902gPqBnw0Mfs_nHr8dnW-V-WztjSB3z8YTN3p2USJ0JfHu9qJq7O5PXRgT6OPwHGWY5z</recordid><startdate>200404</startdate><enddate>200404</enddate><creator>Malathy Sony, S. M.</creator><creator>Sukumar, N.</creator><creator>Ponnuswamy, M. N.</creator><creator>Jayakumar, R.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200404</creationdate><title>Presence of pseudo-peptide bond in the crystal structure of n-(t-butoxycarbonyl)-ε-n′-benzyloxycarbony-l-lysyl-l-isoleucine (boc-lys(obzl)-ile)</title><author>Malathy Sony, S. M. ; Sukumar, N. ; Ponnuswamy, M. N. ; Jayakumar, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2807-55995b5826a09e1cdc68687e3091d26abe8606e1f75bb2d3176cdf55c6fe9c013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>crystal</topic><topic>dipeptide</topic><topic>hydrogen bonds</topic><topic>isoleucine</topic><topic>lysine</topic><topic>pseudo peptide bond</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Malathy Sony, S. M.</creatorcontrib><creatorcontrib>Sukumar, N.</creatorcontrib><creatorcontrib>Ponnuswamy, M. N.</creatorcontrib><creatorcontrib>Jayakumar, R.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Crystal research and technology (1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Malathy Sony, S. M.</au><au>Sukumar, N.</au><au>Ponnuswamy, M. N.</au><au>Jayakumar, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presence of pseudo-peptide bond in the crystal structure of n-(t-butoxycarbonyl)-ε-n′-benzyloxycarbony-l-lysyl-l-isoleucine (boc-lys(obzl)-ile)</atitle><jtitle>Crystal research and technology (1979)</jtitle><addtitle>Cryst. Res. Technol</addtitle><date>2004-04</date><risdate>2004</risdate><volume>39</volume><issue>4</issue><spage>368</spage><epage>374</epage><pages>368-374</pages><issn>0232-1300</issn><eissn>1521-4079</eissn><abstract>The dipeptide Boc‐Lys(OBzl)‐Ile crystallizes in monoclinic space group P21 with cell parameters a = 5.003(1), b = 19.199(3), c = 15.270(2)Å, β =93.42(1)°, V = 1464.1(3)Å3, Z = 2, Dcal = 1.117 Mg/m3 at T = 293 K. The structure was solved by direct methods and refined by full‐matrix least‐squares procedure to a final R = 0.096 and wR = 0.101 using 1379 reflections. The peptide unit is in trans conformation and the molecule takes up an extended conformation. In the lysine side chain, delocalization of electrons and pseudo peptide bond formation is observed at the interaction site of benzyloxycarbonyl group. Both N‐H…O and main chain C‐H…O hydrogen bonds stabilize the molecules in the unit cell in a parallel β‐sheet fashion. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)</abstract><cop>Berlin</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/crat.200310197</doi><tpages>7</tpages></addata></record> |
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subjects | crystal dipeptide hydrogen bonds isoleucine lysine pseudo peptide bond |
title | Presence of pseudo-peptide bond in the crystal structure of n-(t-butoxycarbonyl)-ε-n′-benzyloxycarbony-l-lysyl-l-isoleucine (boc-lys(obzl)-ile) |
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