PDB code | Main view | Title | 1aec |  | CRYSTAL STRUCTURE OF ACTINIDIN-E-64 COMPLEX+ |
1aim |  | CRUZAIN INHIBITED BY BENZOYL-TYROSINE-ALANINE-FLUOROMETHYLKETONE |
1atk |  | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH THE COVALENT INHIBITOR E-64 |
1au0 |  | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC DIACYLAMINOMETHYL KETONE INHIBITOR |
1au2 |  | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PROPANONE INHIBITOR |
1au3 |  | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PYRROLIDINONE INHIBITOR |
1au4 |  | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PYRROLIDINONE INHIBITOR |
1ayu |  | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT SYMMETRIC BISCARBOHYDRAZIDE INHIBITOR |
1ayv |  | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT THIAZOLHYDRAZIDE INHIBITOR |
1ayw |  | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT BENZYLOXYBENZOYLCARBOHYDRAZIDE INHIBITOR |
1bgo |  | CRYSTAL STRUCTURE OF CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT PEPTIDOMIMETIC INHIBITOR |
1bp4 |  | USE OF PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS. CRYSTAL STRUCTURES OF TWO PAPAIN INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S'-SUBSITES. |
1bqi |  | USE OF PAPAIN AS A MODEL FOR THE STRUCTURE-BASED DESIGN OF CATHEPSIN K INHIBITORS. CRYSTAL STRUCTURES OF TWO PAPAIN INHIBITOR COMPLEXES DEMONSTRATE BINDING TO S'-SUBSITES. |
1by8 |  | THE CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN K |
1cjl |  | CRYSTAL STRUCTURE OF A CYSTEINE PROTEASE PROFORM |
1cpj |  | CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN |
1cqd |  | THE 2.1 ANGSTROM STRUCTURE OF A CYSTEINE PROTEASE WITH PROLINE SPECIFICITY FROM GINGER RHIZOME, ZINGIBER OFFICINALE |
1cs8 |  | CRYSTAL STRUCTURE OF PROCATHEPSIN L |
1csb |  | CRYSTAL STRUCTURE OF CATHEPSIN B INHIBITED WITH CA030 AT 2.1 ANGSTROMS RESOLUTION: A BASIS FOR THE DESIGN OF SPECIFIC EPOXYSUCCINYL INHIBITORS |
1cte |  | CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN |
1cvz |  | CRYSTAL STRUCTURE ANALYSIS OF PAPAIN WITH CLIK148(CATHEPSIN L SPECIFIC INHIBITOR) |
1deu |  | CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN X: A CYSTEINE PROTEASE WITH THE PROREGION COVALENTLY LINKED TO THE ACTIVE SITE CYSTEINE |
1ef7 |  | CRYSTAL STRUCTURE OF HUMAN CATHEPSIN X |
1ewl |  | CRYSTAL STRUCTURE OF CRUZAIN BOUND TO WRR-99 |
1ewm |  | THE CYSTEINE PROTEASE CRUZAIN BOUND TO WRR-112 |
1ewo |  | THE CYSTEINE PROTEASE CRUZAIN BOUND TO WRR-204 |
1ewp |  | CRUZAIN BOUND TO MOR-LEU-HPQ |
1f29 |  | CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO A VINYL SULFONE DERIVED INHIBITOR (I) |
1f2a |  | CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO A VINYL SULFONE DERIVED INHIBITOR (II) |
1f2b |  | CRYSTAL STRUCTURE ANALYSIS OF CRUZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (III) |
1f2c |  | CRYSTAL STRUCTURE ANALYSIS OF CRYZAIN BOUND TO VINYL SULFONE DERIVED INHIBITOR (IV) |
1fh0 |  | CRYSTAL STRUCTURE OF HUMAN CATHEPSIN V COMPLEXED WITH AN IRREVERSIBLE VINYL SULFONE INHIBITOR |
1gec |  | GLYCYL ENDOPEPTIDASE-COMPLEX WITH BENZYLOXYCARBONYL-LEUCINE-VALINE-GLYCINE-METHYLENE COVALENTLY BOUND TO CYSTEINE 25 |
1glo |  | Crystal Structure of Cys25Ser mutant of human cathepsin S |
1gmy |  | Cathepsin B complexed with dipeptidyl nitrile inhibitor |
1huc |  | THE REFINED 2.15 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF HUMAN LIVER CATHEPSIN B: THE STRUCTURAL BASIS FOR ITS SPECIFICITY |
1icf |  | CRYSTAL STRUCTURE OF MHC CLASS II ASSOCIATED P41 II FRAGMENT IN COMPLEX WITH CATHEPSIN L |
1ito |  | Crystal Structure Analysis of Bovine Spleen Cathepsin B-E64c complex |
1iwd |  | Proposed Amino Acid Sequence and the 1.63 Angstrom X-ray Crystal Structure of a Plant Cysteine Protease Ervatamin B: Insight into the Structural Basis of its Stability and Substrate Specificity. |
1jqp |  | dipeptidyl peptidase I (cathepsin C), a tetrameric cysteine protease of the papain family |
1k3b |  | Crystal Structure of Human Dipeptidyl Peptidase I (Cathepsin C): Exclusion Domain Added to an Endopeptidase Framework Creates the Machine for Activation of Granular Serine Proteases |
1khp |  | Monoclinic form of papain/ZLFG-DAM covalent complex |
1khq |  | ORTHORHOMBIC FORM OF PAPAIN/ZLFG-DAM COVALENT COMPLEX |
1m6d |  | Crystal structure of human cathepsin F |
1me3 |  | High Resolution Crystal Structure Analysis Of Cruzain non-covalently Bound To A Hydroxymethyl Ketone Inhibitor (II) |
1me4 |  | High Resolution Crystal Structure Analysis Of Cruzain non-covalently Bound To A Hydroxymethyl Ketone Inhibitor (I) |
1meg |  | CRYSTAL STRUCTURE OF A CARICAIN D158E MUTANT IN COMPLEX WITH E-64 |
1mem |  | CRYSTAL STRUCTURE OF CATHEPSIN K COMPLEXED WITH A POTENT VINYL SULFONE INHIBITOR |
1mhw |  | Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides |
1mir |  | RAT PROCATHEPSIN B |
1ms6 |  | Dipeptide Nitrile Inhibitor Bound to Cathepsin S. |
1nb3 |  | Crystal structure of stefin A in complex with cathepsin H: N-terminal residues of inhibitors can adapt to the active sites of endo-and exopeptidases |
1nb5 |  | Crystal structure of stefin A in complex with cathepsin H |
1nl6 |  | Crystal Structure Of The Cysteine Protease Human Cathepsin K In Complex With A Covalent Azepanone Inhibitor |
1nlj |  | CRYSTAL STRUCTURE OF THE CYSTEINE PROTEASE HUMAN CATHEPSIN K IN COMPLEX WITH A COVALENT AZEPANONE INHIBITOR |
1npz |  | Crystal structures of Cathepsin S inhibitor complexes |
1nqc |  | Crystal structures of Cathepsin S inhibitor complexes |
1o0e |  | 1.9 Angstrom Crystal Structure of a plant cysteine protease Ervatamin C |
1pad |  | BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN |
1pbh |  | CRYSTAL STRUCTURE OF HUMAN RECOMBINANT PROCATHEPSIN B AT 3.2 ANGSTROM RESOLUTION |
1pci |  | PROCARICAIN |
1pe6 |  | REFINED X-RAY STRUCTURE OF PAPAIN(DOT)E-64-C COMPLEX AT 2.1-ANGSTROMS RESOLUTION |
1pip |  | CRYSTAL STRUCTURE OF PAPAIN-SUCCINYL-GLN-VAL-VAL-ALA-ALA-P-NITROANILIDE COMPLEX AT 1.7 ANGSTROMS RESOLUTION: NONCOVALENT BINDING MODE OF A COMMON SEQUENCE OF ENDOGENOUS THIOL PROTEASE INHIBITORS |
1pop |  | X-RAY CRYSTALLOGRAPHIC STRUCTURE OF A PAPAIN-LEUPEPTIN COMPLEX |
1ppd |  | RESTRAINED LEAST-SQUARES REFINEMENT OF THE SULFHYDRYL PROTEASE PAPAIN TO 2.0 ANGSTROMS |
1ppn |  | STRUCTURE OF MONOCLINIC PAPAIN AT 1.60 ANGSTROMS RESOLUTION |
1ppo |  | DETERMINATION OF THE STRUCTURE OF PAPAYA PROTEASE OMEGA |
1ppp |  | CRYSTAL STRUCTURE OF PAPAIN-E64-C COMPLEX. BINDING DIVERSITY OF E64-C TO PAPAIN S2 AND S3 SUBSITES |
1q6k |  | Cathepsin K complexed with t-butyl(1S)-1-cyclohexyl-2-oxoethylcarbamate |
1qdq |  | X-RAY CRYSTAL STRUCTURE OF BOVINE CATHEPSIN B-CA074 COMPLEX |
1s4v |  | The 2.0 A crystal structure of the KDEL-tailed cysteine endopeptidase functioning in programmed cell death of Ricinus communis endosperm |
1snk |  | Cathepsin K complexed with carbamate derivatized norleucine aldehyde |
1sp4 |  | Crystal structure of NS-134 in complex with bovine cathepsin B: a two headed epoxysuccinyl inhibitor extends along the whole active site cleft |
1stf |  | THE REFINED 2.4 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF RECOMBINANT HUMAN STEFIN B IN COMPLEX WITH THE CYSTEINE PROTEINASE PAPAIN: A NOVEL TYPE OF PROTEINASE INHIBITOR INTERACTION |
1the |  | CRYSTAL STRUCTURES OF RECOMBINANT RAT CATHEPSIN B AND A CATHEPSIN B-INHIBITOR COMPLEX: IMPLICATIONS FOR STRUCTURE-BASED INHIBITOR DESIGN |
1tu6 |  | Cathepsin K complexed with a ketoamide inhibitor |
1u9q |  | Crystal structure of cruzain bound to an alpha-ketoester |
1u9v |  | Crystal Structure of the Cysteine Protease Human Cathepsin K in Complex with the Covalent Inhibitor NVP-ABE854 |
1u9w |  | Crystal Structure of the Cysteine Protease Human Cathepsin K in Complex with the Covalent Inhibitor NVP-ABI491 |
1u9x |  | Crystal Structure of the Cysteine Protease Human Cathepsin K in Complex with the Covalent Inhibitor NVP-ABJ688 |
1vsn |  | Crystal structure of a potent small molecule inhibitor bound to cathepsin K |
1xkg |  | Crystal structure of the major house dust mite allergen Der p 1 in its pro form at 1.61 A resolution |
1yal |  | CARICA PAPAYA CHYMOPAPAIN AT 1.7 ANGSTROMS RESOLUTION |
1yk7 |  | Cathepsin K complexed with a cyanopyrrolidine inhibitor |
1yk8 |  | Cathepsin K complexed with a cyanamide-based inhibitor |
1yt7 |  | Cathepsin K complexed with a constrained ketoamide inhibitor |
1yvb |  | the Plasmodium falciparum Cysteine Protease Falcipain-2 |
2act |  | CRYSTALLOGRAPHIC REFINEMENT OF THE STRUCTURE OF ACTINIDIN AT 1.7 ANGSTROMS RESOLUTION BY FAST FOURIER LEAST-SQUARES METHODS |
2aim |  | CRUZAIN INHIBITED WITH BENZOYL-ARGININE-ALANINE-FLUOROMETHYLKETONE |
2as8 |  | Crystal structure of mature and fully active Der p 1 allergen |
2ato |  | Crystal structure of Human Cathepsin K in complex with myocrisin |
2aux |  | Cathepsin K complexed with a semicarbazone inhibitor |
2auz |  | Cathepsin K complexed with a semicarbazone inhibitor |
2b1m |  | Crystal structure of a papain-fold protein without the catalytic cysteine from seeds of Pachyrhizus erosus |
2b1n |  | Crystal structure of a papain-fold protein without the catalytic cysteine from seeds of Pachyrhizus erosus |
2bdl |  | Cathepsin K complexed with a pyrrolidine ketoamide-based inhibitor |
2bdz |  | Mexicain from Jacaratia mexicana |
2c0y |  | THE CRYSTAL STRUCTURE OF A CYS25ALA MUTANT OF HUMAN PROCATHEPSIN S |
2cio |  | The high resolution x-ray structure of papain complexed with fragments of the Trypanosoma brucei cysteine protease inhibitor ICP. |
2dc6 |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA073 complex |
2dc7 |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA042 complex |
2dc8 |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA059 complex |
2dc9 |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA074Me complex |
2dca |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA075 complex |
2dcb |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA076 complex |
2dcc |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA077 complex |
2dcd |  | X-ray crystal structure analysis of bovine spleen cathepsin B-CA078 complex |
2djf |  | Crystal Structure of human dipeptidyl peptidase I (Cathepsin C) in complex with the inhibitor Gly-Phe-CHN2 |
2djg |  | Re-determination of the native structure of human dipeptidyl peptidase I (cathepsin C) |
2f1g |  | Cathepsin S in complex with non-covalent 2-(Benzoxazol-2-ylamino)-acetamide |
2f7d |  | A mutant rabbit cathepsin K with a nitrile inhibitor |
2fo5 |  | Crystal structure of recombinant barley cysteine endoprotease B isoform 2 (EP-B2) in complex with leupeptin |
2fq9 |  | Cathepsin S with nitrile inhibitor |
2fra |  | Human Cathepsin S with CRA-27934, a Nitrile Inhibitor |
2frq |  | Human Cathepsin S with Inhibitor CRA-26871 |
2ft2 |  | Human Cathepsin S with Inhibitor CRA-29728 |
2ftd |  | Crystal structure of Cathepsin K complexed with 7-Methyl-Substituted Azepan-3-one compound |
2fud |  | Human Cathepsin S with Inhibitor CRA-27566 |
2fye |  | Mutant Human Cathepsin S with irreversible inhibitor CRA-14013 |
2g6d |  | Human cathepsin S mutant with vinyl sulfone inhibitor CRA-14009 |
2g7y |  | Human Cathepsin S with inhibitor CRA-16981 |
2ghu |  | Crystal structure of falcipain-2 from Plasmodium falciparum |
2h7j |  | Crystal Structure of Cathepsin S in complex with a Nonpeptidic Inhibitor. |
2hh5 |  | Crystal Structure of Cathepsin S in complex with a Zinc mediated non-covalent arylaminoethyl amide |
2hhn |  | Cathepsin S in complex with non covalent arylaminoethyl amide. |
2hxz |  | Crystal Structure of Cathepsin S in complex with a Nonpeptidic Inhibitor (Hexagonal spacegroup) |
2ipp |  | Crystal Structure of the tetragonal form of human liver cathepsin B |
2nqd |  | Crystal structure of cysteine protease inhibitor, chagasin, in complex with human cathepsin L |
2o6x |  | Crystal Structure of ProCathepsin L1 from Fasciola hepatica |
2op3 |  | The structure of cathepsin S with a novel 2-arylphenoxyacetaldehyde inhibitor derived by the Substrate Activity Screening (SAS) method |
2oul |  | The Structure of Chagasin in Complex with a Cysteine Protease Clarifies the Binding Mode and Evolution of a New Inhibitor Family |
2oz2 |  | Crystal structure analysis of cruzain bound to vinyl sulfone derived inhibitor (K11777) |
2p7u |  | The crystal structure of rhodesain, the major cysteine protease of T. brucei rhodesiense, bound to inhibitor K777 |
2p86 |  | The high resolution crystal structure of rohedsain, the major cathepsin L protease from T. brucei rhodesiense, bound to inhibitor K11002 |
2pad |  | BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN |
2pbh |  | CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN B AT 3.3 ANGSTROM RESOLUTION |
2pns |  | 1.9 Angstrom resolution crystal structure of a plant cysteine protease Ervatamin-C refinement with cDNA derived amino acid sequence |
2pre |  | Crystal structure of plant cysteine protease Ervatamin-C complexed with irreversible inhibitor E-64 at 2.7 A resolution |
2r6n |  | Crystal structure of a pyrrolopyrimidine inhibitor in complex with human Cathepsin K |
2r9m |  | Cathepsin S complexed with Compound 15 |
2r9n |  | Cathepsin S complexed with Compound 26 |
2r9o |  | Cathepsin S complexed with Compound 8 |
2vhs |  | Cathsilicatein, a chimera |
2wbf |  | Crystal Structure Analysis of SERA5E from plasmodium falciparum with loop 690-700 ordered |
2xu1 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2xu3 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2xu4 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2xu5 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2yj2 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2yj8 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2yj9 |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2yjb |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
2yjc |  | CATHEPSIN L WITH A NITRILE INHIBITOR |
3ai8 |  | Cathepsin B in complex with the nitroxoline |
3bc3 |  | Exploring inhibitor binding at the S subsites of cathepsin L |
3bcn |  | Crystal structure of a papain-like cysteine protease Ervatamin-A complexed with irreversible inhibitor E-64 |
3bpf |  | Crystal Structure of Falcipain-2 with Its inhibitor, E64 |
3bpm |  | Crystal Structure of Falcipain-3 with Its inhibitor, Leupeptin |
3bwk |  | Crystal Structure of Falcipain-3 with Its inhibitor, K11017 |
3c9e |  | Crystal structure of the cathepsin K : chondroitin sulfate complex. |
3cbj |  | Chagasin-Cathepsin B complex |
3cbk |  | chagasin-cathepsin B |
3ch2 |  | Crystal Structure Analysis of SERA5E from plasmodium falciparum |
3ch3 |  | Crystal Structure Analysis of SERA5E from plasmodium falciparum |
3d6s |  | Crystal structure of mite allergen Der f 1 |
3e1z |  | Crystal structure of the parasite protesase inhibitor chagasin in complex with papain |
3f5v |  | C2 Crystal form of mite allergen DER P 1 |
3f75 |  | Activated Toxoplasma gondii cathepsin L (TgCPL) in complex with its propeptide |
3h6s |  | Strucure of clitocypin - cathepsin V complex |
3h7d |  | The crystal structure of the cathepsin K Variant M5 in complex with chondroitin-4-sulfate |
3h89 |  | A combined crystallographic and molecular dynamics study of cathepsin-L retro-binding inhibitors(compound 4) |
3h8b |  | A combined crystallographic and molecular dynamics study of cathepsin-L retro-binding inhibitors(compound 9) |
3h8c |  | A combined crystallographic and molecular dynamics study of cathepsin-L retro-binding inhibitors (compound 14) |
3hd3 |  | High resolution crystal structure of cruzain bound to the vinyl sulfone inhibitor SMDC-256047 |
3hha |  | Crystal structure of cathepsin L in complex with AZ12878478 |
3hhi |  | Crystal Structure of Cathepsin B from T. brucei in complex with CA074 |
3hwn |  | CATHEPSIN L with AZ13010160 |
3i06 |  | Crystal structure of cruzain covalently bound to a purine nitrile |
3iej |  | Pyrazole-based Cathepsin S Inhibitors with Arylalkynes as P1 Binding Elements |
3ima |  | Complex strcuture of tarocystatin and papain |
3ioq |  | Crystal structure of the Carica candamarcensis cysteine protease CMS1MS2 in complex with E-64. |
3iut |  | The Crystal Structure of Cruzain in Complex with a Tetrafluorophenoxymethyl Ketone Inhibitor |
3iv2 |  | Crystal structure of mature apo-Cathepsin L C25A mutant |
3k24 |  | Crystal structure of mature apo-Cathepsin L C25A mutant in complex with Gln-Leu-Ala peptide |
3k9m |  | Cathepsin B in complex with stefin A |
3kfq |  | Unreduced cathepsin V in complex with stefin A |
3kku |  | Cruzain in complex with a non-covalent ligand |
3kse |  | Unreduced cathepsin L in complex with stefin A |
3kw9 |  | X-ray structure of Cathepsin K covalently bound to a triazine ligand |
3kwb |  | Structure of CatK covalently bound to a dioxo-triazine inhibitor |
3kwn |  | Cathepsin S in complex with Thioether Acetamide P3 inhibitor |
3kwz |  | Cathepsin K in complex with a non-selective 2-cyano-pyrimidine inhibitor |
3kx1 |  | Cathepsin K in complex with a selective 2-cyano-pyrimidine inhibitor |
3lfy |  | CTD of Tarocystatin in complex with papain |
3lxs |  | Crystal structure analysis of cruzain bound to vinyl sulfone derived inhibitor (WRR483) |
3mor |  | Crystal structure of Cathepsin B from Trypanosoma Brucei |
3mpe |  | Crystal structure of human Cathepsin-S C25S mutant with bound drug |
3mpf |  | Crystal structure of human Cathepsin-S C25S mutant with bound drug |
3n3g |  | 4-(3-Trifluoromethylphenyl)-pyrimidine-2-carbonitrile as cathepsin S inhibitors: N3, not N1 is critically important |
3n4c |  | 6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors |
3o0u |  | Cathepsin K covalently bound to a cyano-pyrimidine inhibitor with improved selectivity over hERG |
3o1g |  | Cathepsin K covalently bound to a 2-cyano pyrimidine inhibitor with a benzyl P3 group. |
3of8 |  | Structural Basis for Reversible and Irreversible Inhibition of Human Cathepsin L by their Respective Dipeptidyl Glyoxal and Diazomethylketone Inhibitors |
3of9 |  | Structural Basis for Irreversible Inhibition of Human Cathepsin L by a Diazomethylketone Inhibitor |
3ois |  | Crystal Structure Xylellain, a cysteine protease from Xylella fastidiosa |
3ovx |  | Cathepsin S in complex with a covalent inhibitor with an aldehyde warhead |
3ovz |  | Cathepsin K in complex with a covalent inhibitor with a ketoamide warhead |
3p5u |  | Actinidin from Actinidia arguta planch (Sarusashi) |
3p5v |  | Actinidin from Actinidia arguta planch (Sarusashi) |
3p5w |  | Actinidin from Actinidia arguta planch (Sarusashi) |
3p5x |  | Actinidin from Actinidia arguta planch (Sarusashi) |
3pbh |  | REFINED CRYSTAL STRUCTURE OF HUMAN PROCATHEPSIN B AT 2.5 ANGSTROM RESOLUTION |
3pdf |  | Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C |
3pnr |  | Structure of PbICP-C in complex with falcipain-2 |
3qj3 |  | Structure of digestive procathepsin L2 proteinase from Tenebrio molitor larval midgut |
3qsd |  | Structure of cathepsin B1 from Schistosoma mansoni in complex with CA074 inhibitor |
3qt4 |  | Structure of digestive procathepsin L 3 of Tenebrio molitor larval midgut |
3rvv |  | Crystal structure of Der f 1 complexed with Fab 4C1 |
3rvw |  | Crystal structure of Der p 1 complexed with Fab 4C1 |
3rvx |  | Crystal structure of Der p 1 complexed with Fab 4C1 |
3s3q |  | Structure of cathepsin B1 from Schistosoma mansoni in complex with K11017 inhibitor |
3s3r |  | Structure of cathepsin B1 from Schistosoma mansoni in complex with K11777 inhibitor |
3tnx |  | Structure of the precursor of a thermostable variant of papain at 2.6 Angstroem resolution |
3u8e |  | Crystal Structure of Cysteine Protease from Bulbs of Crocus sativus at 1.3 A Resolution |
3usv |  | Structure of the precursor of a thermostable variant of papain at 3.8 A resolution from a crystal soaked at pH 4 |
4axl |  | HUMAN CATHEPSIN L APO FORM WITH ZN |
4axm |  | TRIAZINE CATHEPSIN INHIBITOR COMPLEX |
4bpv |  | 4BPV |
4bqv |  | 4BQV |
4bs5 |  | MOUSE CATHEPSIN S WITH COVALENT LIGAND |
4bs6 |  | 4BS6 |
4bsq |  | MOUSE CATHEPSIN S WITH COVALENT LIGAND |
4cdc |  | Human DPP1 in complex with (2S)-2-amino-N-((1S)-1-cyano-2-(4- phenylphenyl)ethyl)butanamide |
4cdd |  | Human DPP1 in complex with (2S)-N-((1S)-1-cyano-2-(4-(4-cyanophenyl) phenyl)ethyl)piperidine-2-carboxamide |
4cde |  | Human DPP1 in complex with 4-amino-N-((1S)-1-cyano-2-(4-(4- cyanophenyl)phenyl)ethyl)tetrahydropyran-4-carboxamide |
4cdf |  | Human DPP1 in complex with (2S,4S)-N-((1S)-1-cyano-2-(4-(4- cyanophenyl)phenyl)ethyl)-4-hydroxy-piperidine-2-carboxamide |
4ci7 |  | The crystal structure of the cysteine protease and lectin-like domains of Cwp84, a surface layer associated protein of Clostridium difficile |
4d59 |  | 4D59 |
4d5a |  | 4D5A |
4dmx |  | Cathepsin K inhibitor |
4dmy |  | Cathepsin K inhibitor |
4hwy |  | Trypanosoma brucei procathepsin B solved from 40 fs free-electron laser pulse data by serial femtosecond X-ray crystallography |
4i04 |  | Structure of zymogen of cathepsin B1 from Schistosoma mansoni |
4i05 |  | Structure of intermediate processing form of cathepsin B1 from Schistosoma mansoni |
4i07 |  | Structure of mature form of cathepsin B1 from Schistosoma mansoni |
4klb |  | Crystal Structure of Cruzain in complex with the non-covalent inhibitor Nequimed176 |
4kp9 |  | 4KP9 |
4mzo |  | 4MZO |
4mzs |  | 4MZS |
4n4z |  | Trypanosoma brucei procathepsin B structure solved by Serial Microcrystallography using synchrotron radiation |
4n79 |  | 4N79 |
4n8w |  | 4N8W |
4oel |  | 4OEL |
4oem |  | 4OEM |
4p6e |  | 4P6E |
4p6g |  | 4P6G |
4pad |  | BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN |
4pi3 |  | 4PI3 |
4pp1 |  | 4PP1 |
4pp2 |  | 4PP2 |
4qh6 |  | 4QH6 |
4qrg |  | 4QRG |
4qrv |  | 4QRV |
4qrx |  | 4QRX |
4w5b |  | 4W5B |
4w5c |  | 4W5C |
4x6h |  | 4X6H |
4x6i |  | 4X6I |
4x6j |  | 4X6J |
4xui |  | 4XUI |
4yv8 |  | 4YV8 |
4yva |  | 4YVA |
4yyq |  | 4YYQ |
4yyr |  | 4YYR |
4yys |  | 4YYS |
4yyu |  | 4YYU |
4yyv |  | 4YYV |
4yyw |  | 4YYW |
5a24 |  | 5A24 |
5ef4 |  | 5EF4 |
5egw |  | 5EGW |
5f02 |  | 5F02 |
5fpw |  | 5FPW |
5i4h |  | 5I4H |
5j94 |  | 5J94 |
5ja7 |  | 5JA7 |
5jh3 |  | 5JH3 |
5pad |  | BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN |
6pad |  | BINDING OF CHLOROMETHYL KETONE SUBSTRATE ANALOGUES TO CRYSTALLINE PAPAIN |
7pck |  | CRYSTAL STRUCTURE OF WILD TYPE HUMAN PROCATHEPSIN K |
8pch |  | CRYSTAL STRUCTURE OF PORCINE CATHEPSIN H DETERMINED AT 2.1 ANGSTROM RESOLUTION: LOCATION OF THE MINI-CHAIN C-TERMINAL CARBOXYL GROUP DEFINES CATHEPSIN H AMINOPEPTIDASE FUNCTION |
9pap |  | STRUCTURE OF PAPAIN REFINED AT 1.65 ANGSTROMS RESOLUTION |