THE STRUCTURE OF A SYNTHETIC PEPSIN INHIBITOR COMPLEXED WITH ENDOTHIAPEPSIN

被引：54

作者：

COOPER, J

FOUNDLING, S

HEMMINGS, A

BLUNDELL, T

JONES, DM

HALLETT, A

SZELKE, M

机构：

[1] UNIV LONDON BIRKBECK COLL, DEPT CRYSTALLOG, MOLEC BIOL LAB, MALET ST, LONDON WC1E 7HX, ENGLAND

[2] ROYAL POSTGRAD MED SCH, DEPT CHEM PATHOL, LONDON W12 0HS, ENGLAND

来源：

EUROPEAN JOURNAL OF BIOCHEMISTRY | 1987年 / 169卷 / 01期

关键词：

D O I：

10.1111/j.1432-1033.1987.tb13600.x

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：215 / 221

页数：7

共 37 条

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[7] THE SYNTHESIS, PURIFICATION, AND EVALUATION OF A CHROMOPHORIC SUBSTRATE FOR PEPSIN AND OTHER ASPARTYL PROTEASES - DESIGN OF A SUBSTRATE BASED ON SUBSITE PREFERENCES
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[8] HIGH-RESOLUTION X-RAY ANALYSES OF RENIN INHIBITOR-ASPARTIC PROTEINASE COMPLEXES
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COOPER, J
WATSON, FE
CLEASBY, A
PEARL, LH
SIBANDA, BL
HEMMINGS, A
WOOD, SP
BLUNDELL, TL
VALLER, MJ
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SZELKE, M
[J]. NATURE, 1987, 327 (6120) : 349 - 352
[9] FRUTON JS, 1976, ADV ENZYMOL RAMB, V44, P1
[10] HALLETT A, 1985, ASPARTIC PROTEINASES, P467

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