(Q27650729)

7

0 references

Mariusz Jaskólski

6

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Izabela Redzynia

1

object named as

Izabela Redzynia

0 references

Magnus Abrahamson

3

object named as

Magnus Abrahamson

0 references

Joanne C Krupa

5

object named as

Joanne C Krupa

0 references

author name string

Anna Ljunggren

2

0 references

John S Mort

Journal of Biological Chemistry

4

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language of work or name

English

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publication date

15 August 2008

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published in

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volume

283

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page(s)

22815-25

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issue

33

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cites work

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Crystal structure of porcine cathepsin H determined at 2.1 A resolution: location of the mini-chain C-terminal carboxyl group defines cathepsin H aminopeptidase function

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The crystal structure of human dipeptidyl peptidase I (cathepsin C) in complex with the inhibitor Gly-Phe-CHN2.

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Crystal structure of human procathepsin X: a cysteine protease with the proregion covalently linked to the active site cysteine

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Major increase in endopeptidase activity of human cathepsin B upon removal of occluding loop contacts.

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Structure of rat procathepsin B: model for inhibition of cysteine protease activity by the proregion

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Cystatin inhibition of cathepsin B requires dislocation of the proteinase occluding loop. Demonstration By release of loop anchoring through mutation of his110.

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Crystal structure of the parasite protease inhibitor chagasin in complex with a host target cysteine protease

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Solution structure and backbone dynamics of the Trypanosoma cruzi cysteine protease inhibitor chagasin

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The structure of chagasin in complex with a cysteine protease clarifies the binding mode and evolution of an inhibitor family

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The role of conserved residues of chagasin in the inhibition of cysteine peptidases

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Insect small nuclear RNA gene promoters evolve rapidly yet retain conserved features involved in determining promoter activity and RNA polymerase specificity.

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S2' substrate specificity and the role of His110 and His111 in the exopeptidase activity of human cathepsin B.

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The Purification of Papain by Affinity Chromatography

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Structural basis for the biological specificity of cystatin C. Identification of leucine 9 in the N-terminal binding region as a selectivity-conferring residue in the inhibition of mammalian cysteine peptidases

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A linear equation that describes the steady-state kinetics of enzymes and subcellular particles interacting with tightly bound inhibitors

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Processing of X-ray diffraction data collected in oscillation mode

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MOLREP: an Automated Program for Molecular Replacement

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Refinement of macromolecular structures by the maximum-likelihood method

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A graphical user interface to the CCP4 program suite

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Use of TLS parameters to model anisotropic displacements in macromolecular refinement

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Free R value: a novel statistical quantity for assessing the accuracy of crystal structures

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PROCHECK: a program to check the stereochemical quality of protein structures

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Crystal structures of human procathepsin B at 3.2 and 3.3 Angstroms resolution reveal an interaction motif between a papain-like cysteine protease and its propeptide

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Scaling and assessment of data quality

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