EC 3.4.22.38 - cathepsin K
3D structures of EC 3.4.22.38 - cathepsin K in Protein Data Bank
updated: 6 January 2022, 2:15
In total: 67 PDB structures of EC 3.4.22.38 - cathepsin K:
- 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
- 1by8: The Crystal Structure of Human Procathepsin K
- 7pck: Crystal Structure of Wild Type Human Procathepsin K
- 3o1g: Cathepsin K Covalently Bound to a 2-cyano Pyrimidine Inhibitor with a Benzyl P3 Group.
- 1mem: Crystal Structure of Cathepsin K Complexed with a Potent Vinyl Sulfone Inhibitor
- 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
- 6ql8: Cathepsin-k in Complex with Miv-711
- 3kx1: Cathepsin K in Complex with a Selective 2-cyano-pyrimidine Inhibitor
- 3kwz: Cathepsin K in Complex with a Non-selective 2-cyano- Pyrimidine Inhibitor
- 3kwb: Structure of Catk Covalently Bound to a Dioxo-triazine Inhibitor
- 3kw9: X-ray Structure of Cathepsin K Covalently Bound to a Triazine Ligand
- 1q6k: Cathepsin K Complexed with T-butyl(1s)-1-cyclohexyl-2- Oxoethylcarbamate
- 3h7d: The Crystal Structure of The Cathepsin K Variant M5 in Complex with Chondroitin-4-sulfate
- 1snk: Cathepsin K Complexed with Carbamate Derivatized Norleucine Aldehyde
- 6qlm: Cathepsin-k in Complex with Miv-701
- 1tu6: Cathepsin K Complexed with a Ketoamide Inhibitor
- 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
- 3c9e: Crystal Structure of The Cathepsin K : Chondroitin Sulfate Complex.
- 1vsn: Crystal Structure of a Potent Small Molecule Inhibitor Bound to Cathepsin K
- 6qlw: Cathepsin-k in Complex with Miv-710
- 6qlx: Cathepsin-k in Complex with Fluoro-oxa-azabicyclo[3.3.0]octanyl Containing Inhibitor
- 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
- 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
- 2bdl: Cathepsin K Complexed with a Pyrrolidine Ketoamide-based Inhibitor
- 2r6n: Crystal Structure of a Pyrrolopyrimidine Inhibitor in Complex with Human Cathepsin K
- 6bki: Crystal Structure of T101A Variant Mouse Cathepsin K at 2.94 Angstrom Resolution.
- 6ash: Crystal Structure of Human Cathepsin K with a Non-active Site Inhibitor at 1.42 Angstrom Resolution
- 2f7d: A Mutant Rabbit Cathepsin K with a Nitrile Inhibitor
- 2ftd: Crystal Structure of Cathepsin K Complexed with 7-methyl- Substituted Azepan-3-one Compound
- 5z5o: Structure of Pycnonodysostosis Disease Related I249T Mutant of Human Cathepsin K
- 6pxf: Structure of Human Cathepsin K with an Ectosteric Inhibitor at 1.85 Angstrom Resolution
- 3ovz: Cathepsin K in Complex with a Covalent Inhibitor with a Ketoamide Warhead
- 3o0u: Cathepsin K Covalently Bound to a Cyano-pyrimidine Inhibitor with Improved Selectivity over Herg
- 6qbs: The Alkyne Moiety as a Latent Electrophile in Irreversible Covalent Small Molecule Inhibitors of Cathepsin K
- 4dmx: Cathepsin K Inhibitor
- 4dmy: Cathepsin K Inhibitor
- 6qm0: Cathepsin-k in Complex with Amino-oxaazabicyclo[3.3.0]octanyl Containing Inhibitor
- 6hgy: Crystal Structure of Cathepsin K with N-desmethyl Thalassospiramide C
- 4n79: Structure of Cathepsin K-dermatan Sulfate Complex
- 4n8w: Cathepsin K - Chondroitin Sulfate Complex
- 5tun: Crystal Structure of Uninhibited Human Cathepsin K at 1.62 Angstrom Resolution
- 5tdi: Crystal Structure of Cathepsin K with a Covalently-linked Inhibitor at 1.4 Angstrom Resolution.
- 5t6u: Crystal Structure of Mouse Cathepsin K at 2.9 Angstroms Resolution.
- 5jh3: Human Cathepsin K Mutant C25S
- 5ja7: Human Cathepsin K Mutant C25S in Complex with The Allosteric Effector Nsc94914
- 5j94: Human Cathepsin K Mutant C25S in Complex with The Allosteric Effector Nsc13345
- 4yva: Cathepsin K Co-crystallized with Actinomycetes Extract
- 4yv8: Crystal Structure of Cathepsin K Bound to The Covalent Inhibitor Lichostatinal
- 4x6h: Development of N-(functionalized Benzoyl)-homocycloleucyl- Glycinonitriles as Potent Cathepsin K Inhibitors.
- 4x6i: Development of N-(functionalized Benzoyl)-homocycloleucyl- Glycinonitriles as Potent Cathepsin K Inhibitors.
- 4x6j: Development of N-(functionalized Benzoyl)-homocycloleucyl- Glycinonitriles as Potent Cathepsin K Inhibitors.
- 7nxm: Structure of Human Cathepsin K in Complex with The Selective Activity- Based Probe Gu3416
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