The structure of active serpin 1K from Manduca sexta (Q27618619)

2

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B Canagarajah

3

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H Jiang

4

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M Kanost

5

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E J Goldsmith

Human plasma proteinase inhibitors

6

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publication date

15 January 1999

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published in

Structure

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volume

7

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issue

1

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page(s)

103-9

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cites work

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Implications of the three-dimensional structure of alpha 1-antitrypsin for structure and function of serpins

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The structural puzzle of how serpin serine proteinase inhibitors work

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Crystal structure of plakalbumin, a proteolytically nicked form of ovalbumin. Its relationship to the structure of cleaved alpha-1-proteinase inhibitor

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Human alpha 1-proteinase inhibitor. Crystal structure analysis of two crystal modifications, molecular model and preliminary analysis of the implications for function

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Structural basis of latency in plasminogen activator inhibitor-1

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Kinetically controlled folding of the serpin plasminogen activator inhibitor 1

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An atlas of serpin conformations.

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Crystal structure of an uncleaved serpin reveals the conformation of an inhibitory reactive loop

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Crystal structure of ovalbumin as a model for the reactive centre of serpins

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Inhibitory conformation of the reactive loop of alpha 1-antitrypsin

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The native strains in the hydrophobic core and flexible reactive loop of a serine protease inhibitor: crystal structure of an uncleaved alpha1-antitrypsin at 2.7 A

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Crystallographic refinement of Japanese quail ovomucoid, a Kazal-type inhibitor, and model building studies of complexes with serine proteases

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Serpin-resistant mutants of human tissue-type plasminogen activator

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Effects of mutations in the hinge region of serpins

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The intact and cleaved human antithrombin III complex as a model for serpin–proteinase interactions

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Biological implications of a 3 A structure of dimeric antithrombin

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Mobile reactive centre of serpins and the control of thrombosis

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Immunologic evidence for insertion of the reactive-bond loop of antithrombin into the A beta-sheet of the inhibitor during trapping of target proteinases

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Analysis of the plasma elimination kinetics and conformational stabilities of native, proteinase-complexed, and reactive site cleaved serpins: comparison of alpha 1-proteinase inhibitor, alpha 1-antichymotrypsin, antithrombin III, alpha 2-antiplasmi

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Structural insights into serpin-protease complexes reveal the inhibitory mechanism of serpins

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Major proteinase movement upon stable serpin-proteinase complex formation

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Serpin-protease complexes are trapped as stable acyl-enzyme intermediates

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Characterization and functional analysis of 12 naturally occurring reactive site variants of serpin-1 from Manduca sexta

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Serpin tertiary structure transformation

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Role of the catalytic serine in the interactions of serine proteinases with protein inhibitors of the serpin family. Contribution of a covalent interaction to the binding energy of serpin-proteinase complexes.

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Distortion of the active site of chymotrypsin complexed with a serpin

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Expression and characterization of recombinant Manduca sexta serpin-1B and site-directed mutants that change its inhibitory selectivity

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AMoRe: an automated package for molecular replacement

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Improved Fourier coefficients for maps using phases from partial structures with errors

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The CCP4 suite: programs for protein crystallography

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Protein folding and association: insights from the interfacial and thermodynamic properties of hydrocarbons

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