+Search query
-Structure paper
Title | Design of potent selective zinc-mediated serine protease inhibitors. |
---|---|
Journal, issue, pages | Nature, Vol. 391, Page 608-612, Year 1998 |
Publish date | Jul 21, 1999 (structure data deposition date) |
Authors | Katz, B.A. / Clark, J.M. / Finer-Moore, J.S. / Jenkins, T.E. / Johnson, C.R. / Ross, M.J. / Luong, C. / Moore, W.R. / Stroud, R.M. |
External links | Nature / PubMed:9468142 |
Methods | X-ray diffraction |
Resolution | 1.37 - 2.2 Å |
Structure data | PDB-1c1n: PDB-1c1o: PDB-1c1p: PDB-1c1q: PDB-1c1r: PDB-1c1t: PDB-1c1u: PDB-1c1v: PDB-1c1w: PDB-1c2d: PDB-1c2e: PDB-1c2f: PDB-1c2g: PDB-1c2h: PDB-1c2i: PDB-1c2j: PDB-1c2k: PDB-1c2l: PDB-1c2m: PDB-1xuf: PDB-1xug: PDB-1xuh: PDB-1xui: PDB-1xuj: PDB-1xuk: |
Chemicals | ChemComp-CA: ChemComp-ZN: ChemComp-SO4: ChemComp-BEN: ChemComp-HOH: ChemComp-MG: ChemComp-BAI: ChemComp-DMS: ChemComp-BAB: ChemComp-NA: ChemComp-BAH: ChemComp-BAK: ChemComp-CL: ChemComp-ABI: ChemComp-BAZ: ChemComp-CO: ChemComp-BAO: ChemComp-BOZ: |
Source |
|
Keywords | HYDROLASE/HYDROLASE INHIBITOR / ZN(II)-MEDIATED SERINE PROTEASE INHIBITORS / PH DEPENDENCE / ZN(II) AFFINITY STUCTURE-BASED DRUG DESIGN / SERINE PROTEASE / HYDROLASE-HYDROLASE INHIBITOR COMPLEX / SERINE PROTEASE SERINE PROTEASE/INHIBITOR / SERINE PROTEASE/INHIBITOR / BLOOD CLOTTING/HYDROLASE INHIBITOR / BLOOD CLOTTING-HYDROLASE INHIBITOR COMPLEX / BLOOD CLOTTING / COMPLEX / TRYPSIN-ZN+2-SMALL MOLECULE LIGAND / DESIGNED SMALL MOLECULE LIGAND WITH NANOMOLAR AFFINITY / TRYPSIN-COBALT-SMALL MOLECULE LIGAND / DESIGNED SMALL MOLECULE LIGAND WITH MICROMOLAR AFFINITY / TRYPSIN-SMALL MOLECULE LIGAND / TRYPSIN-SULFATE-SMALL MOLECULE LIGAND |