OXALOPEPTIDES AS CORE MOTIFS FOR PROTEIN DESIGN

被引:12
作者
RANGANATHAN, D [1 ]
VAISH, NK [1 ]
SHAH, K [1 ]
ROY, R [1 ]
MADHUSUDANAN, KP [1 ]
机构
[1] CENT DRUG RES INST,LUCKNOW 226001,UTTAR PRADESH,INDIA
关键词
D O I
10.1039/c39930000092
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxalopeptides are demonstrated to be useful core motifs for bi-directional chain elongation leading to peptide homologues with interesting folding behaviour, thus constituting a useful strategy for protein backbone modification.
引用
收藏
页码:92 / 94
页数:3
相关论文
共 6 条
[1]  
Bornwater JT, 1912, RECL TRAV CH PAYS-BA, V31, P105
[2]   STEREOISOMERISM OF N,N'-OXALYLBIS-(ALANINE) DERIVATIVES [J].
HEARN, WR ;
HENDRY, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1957, 79 (19) :5213-5217
[3]   L-PROLINE-N-OXALIC ANHYDRIDE [J].
HEARN, WR ;
WORTHINGTON, RE .
JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (12) :4072-+
[4]   TRANSFORMATION OF C-TERMINAL SERINE AND THREONINE EXTENDED PRECURSORS INTO C-TERMINAL ALPHA-AMIDATED PEPTIDES - A POSSIBLE CHEMICAL-MODEL FOR THE ALPHA-AMIDATING ACTION OF PITUITARY ENZYMES [J].
RANGANATHAN, D ;
SAINI, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (03) :1042-1044
[5]  
SPATOLA AF, 1983, CHEM BIOCH AMINO ACI, V7, P268
[6]   CHIRAL (MACROCYCLIC) SULFIDE-CONTAINING AND SULFIDE/ALKYLAMINO-CONTAINING LIGANDS FOR NICKEL-CATALYZED GRIGNARD CROSS-COUPLING REACTIONS [J].
VRIESEMA, BK ;
LEMAIRE, M ;
BUTER, J ;
KELLOGG, RM .
JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (26) :5169-5177