scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0969-2126(00)00108-8 |
P698 | PubMed publication ID | 10745011 |
P2093 | author name string | V Turk | |
D Turk | |||
B Turk | |||
L Juliano | |||
G Guncar | |||
A Karaoglanovic-Carmona | |||
I Klemencic | |||
P2860 | cites work | Design of potent and selective human cathepsin K inhibitors that span the active site | Q24651743 |
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Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice | Q36791739 | ||
Cathepsin K, but not cathepsins B, L, or S, is abundantly expressed in human osteoclasts | Q36800896 | ||
Modulation of invasive properties of murine squamous carcinoma cells by heterologous expression of cathepsin B and cystatin C. | Q40925415 | ||
Exocytosis of active cathepsin B enzyme activity at pH 7.0, inhibition and molecular mass | Q40935441 | ||
Invariant chain structure and MHC class II function | Q40968427 | ||
Revised definition of substrate binding sites of papain-like cysteine proteases | Q41730414 | ||
Human cathepsin O2, a matrix protein-degrading cysteine protease expressed in osteoclasts. Functional expression of human cathepsin O2 in Spodoptera frugiperda and characterization of the enzyme | Q42064898 | ||
Accurate bond and angle parameters for X-ray protein structure refinement | Q56485700 | ||
Structure of actinidin, after refinement at 1.7 A resolution | Q67247280 | ||
CA074 methyl ester: a proinhibitor for intracellular cathepsin B | Q67587602 | ||
Novel epoxysuccinyl peptides. A selective inhibitor of cathepsin B, in vivo | Q70136102 | ||
Evidence for extracellularly acting cathepsins mediating thyroid hormone liberation in thyroid epithelial cells | Q71033250 | ||
Extracellular presence of the lysosomal proteinase cathepsin B in rheumatoid synovium and its activity at neutral pH | Q71347962 | ||
Role of the occluding loop in cathepsin B activity | Q71973705 | ||
Structure based development of novel specific inhibitors for cathepsin L and cathepsin S in vitro and in vivo | Q73077056 | ||
E-64 analogues as inhibitors of cathepsin B. On the role of the absolute configuration of the epoxysuccinyl group | Q73837899 | ||
Substrate/propeptide-derived endo-epoxysuccinyl peptides as highly potent and selective cathepsin B inhibitors | Q74173020 | ||
Impaired invariant chain degradation and antigen presentation and diminished collagen-induced arthritis in cathepsin S null mice | Q74595052 | ||
Intracellular proteolytic cleavage of 9-cis-retinoic acid receptor alpha by cathepsin L-type protease is a potential mechanism for modulating thyroid hormone action | Q77630871 | ||
Crystal structure of MHC class II-associated p41 Ii fragment bound to cathepsin L reveals the structural basis for differentiation between cathepsins L and S. | Q27617244 | ||
The refined 2.15 A X-ray crystal structure of human liver cathepsin B: the structural basis for its specificity | Q27651464 | ||
Structure of papain refined at 1.65 A resolution | Q27729147 | ||
Crystal structure of cathepsin B inhibited with CA030 at 2.0-A resolution: A basis for the design of specific epoxysuccinyl inhibitors | Q27730182 | ||
Crystal structure of the wild-type human procathepsin B at 2.5 A resolution reveals the native active site of a papain-like cysteine protease zymogen | Q27743415 | ||
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 | Q27748903 | ||
Rapid automated molecular replacement by evolutionary search | Q27860711 | ||
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency | Q28284581 | ||
Emerging roles for cysteine proteases in human biology | Q28306260 | ||
Cathepsin S required for normal MHC class II peptide loading and germinal center development | Q28611850 | ||
Cathepsin L: critical role in Ii degradation and CD4 T cell selection in the thymus | Q28613227 | ||
Human cathepsin X: a novel cysteine protease of the papain family with a very short proregion and unique insertions | Q32021129 | ||
Enzymatically active lysosomal proteases are associated with amyloid deposits in Alzheimer brain | Q33590450 | ||
The lysosomal cysteine proteases | Q33689936 | ||
Lysosomal cysteine proteases: more than scavengers | Q33857460 | ||
Human cathepsin X: A cysteine protease with unique carboxypeptidase activity | Q33875510 | ||
Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo | Q35558255 | ||
P433 | issue | 3 | |
P921 | main subject | crystal structure | Q895901 |
P304 | page(s) | 305-13 | |
P577 | publication date | 2000-03-15 | |
P1433 | published in | Structure | Q15709970 |
P1476 | title | Crystal structure of cathepsin X: a flip-flop of the ring of His23 allows carboxy-monopeptidase and carboxy-dipeptidase activity of the protease | |
P478 | volume | 8 |
Q35683586 | 6. Cathepsin K inhibitors: their potential as anti-osteoporosis agents |
Q37323524 | Averaged kick maps: less noise, more signal... and probably less bias |
Q83993707 | Carboxypeptidase cathepsin X mediates beta2-integrin-dependent adhesion of differentiated U-937 cells |
Q40426125 | Carboxypeptidases cathepsins X and B display distinct protein profile in human cells and tissues |
Q43716338 | Cathepsins X and B display distinct activity profiles that can be exploited for inhibitor design |
Q44935351 | Comprehensive search for cysteine cathepsins in the human genome |
Q44949896 | Cyclic, linear, cycloretro-isomer, and cycloretro-inverso peptides derived from the C-terminal sequence of bradykinin as substrates or inhibitors of serine and cysteine proteases |
Q26860406 | Cysteine cathepsins: from structure, function and regulation to new frontiers |
Q91690107 | Cysteine-type cathepsins promote the effector phase of acute cutaneous delayed-type hypersensitivity reactions |
Q35053426 | Development of activity-based probes for cathepsin X. |
Q31444536 | Epoxysuccinyl peptide-derived affinity labels for cathepsin B. |
Q35167690 | FEM: feature-enhanced map. |
Q24791513 | Importance of lysosomal cysteine proteases in lung disease |
Q36790438 | Interpretation of ensembles created by multiple iterative rebuilding of macromolecular models |
Q36713744 | Iterative-build OMIT maps: map improvement by iterative model building and refinement without model bias |
Q37907192 | LFA-1 fine-tuning by cathepsin X. |
Q26749121 | Lysosomal cathepsins and their regulation in aging and neurodegeneration |
Q44068250 | Lysosomal cathepsins: structure, role in antigen processing and presentation, and cancer |
Q42156127 | MAIN software for density averaging, model building, structure refinement and validation. |
Q53347423 | Molecular cloning, expression, and enzymatic analysis of cathepsin X from starfish (Asterina pectinifera). |
Q30389896 | Novel proteases from the genome of the carnivorous plant Drosera capensis: Structural prediction and comparative analysis |
Q24654617 | PHENIX: a comprehensive Python-based system for macromolecular structure solution |
Q79079855 | Phylogeny of Antigen‐Processing Enzymes: Cathepsins of a Cephalochordate, an Agnathan and a Bony Fish |
Q37631800 | Polder maps: improving OMIT maps by excluding bulk solvent. |
Q46286189 | Purification and characterization of cathepsin B-like cysteine protease from cotyledons of daikon radish, Raphanus sativus |
Q46819743 | Recombinant human cathepsin X is a carboxymonopeptidase only: a comparison with cathepsins B and L. |
Q42157735 | S2' substrate specificity and the role of His110 and His111 in the exopeptidase activity of human cathepsin B. |
Q27664635 | Stefin A displaces the occluding loop of cathepsin B only by as much as required to bind to the active site cleft |
Q48031305 | Structural and functional characterization of Falcipain-2, a hemoglobinase from the malarial parasite Plasmodium falciparum |
Q27636471 | Structure of human dipeptidyl peptidase I (cathepsin C): exclusion domain added to an endopeptidase framework creates the machine for activation of granular serine proteases |
Q30163955 | Structures of sortase B from Staphylococcus aureus and Bacillus anthracis reveal catalytic amino acid triad in the active site |
Q47069564 | The Caenorhabditis elegans cathepsin Z-like cysteine protease, Ce-CPZ-1, has a multifunctional role during the worms' development |
Q27639638 | The crystal structure of human cathepsin F and its implications for the development of novel immunomodulators |
Q34956890 | The role of cathepsin X in cell signaling |
Q27860678 | Towards automated crystallographic structure refinement with phenix.refine |
Q27679343 | Ultrahigh and High Resolution Structures and Mutational Analysis of Monomeric Streptococcus pyogenes SpeB Reveal a Functional Role for the Glycine-rich C-terminal Loop |
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