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| Title | Synthesis, evaluation, and crystallographic analysis of L-371,912: A potent and selective active-site thrombin inhibitor. |
|---|---|
| Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 7, Page 67-72, Year 1997 |
| Publish date | Dec 6, 1996 (structure data deposition date) |
Authors | Lyle, T.A. / Chen, Z.G. / Appleby, S.D. / Freidinger, R.M. / Gardell, S.J. / Lewis, S.D. / Li, Y. / Lyle, E.A. / Lynch, J.J. / Mulichak, A.M. ...Lyle, T.A. / Chen, Z.G. / Appleby, S.D. / Freidinger, R.M. / Gardell, S.J. / Lewis, S.D. / Li, Y. / Lyle, E.A. / Lynch, J.J. / Mulichak, A.M. / Ng, A.S. / NaylorOlsen, A.M. / Sanders, W.M. |
External links | Search PubMed |
| Methods | X-ray diffraction |
| Resolution | 1.8 Å |
| Structure data | ![]() PDB-1tom: |
| Chemicals | ![]() ChemComp-MIN: ![]() ChemComp-HOH: |
| Source |
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Keywords | BLOOD COAGULATION/HYDROLASE INHIBITOR / HYDROLASE / SERINE PROTEASE / KRINGLE / DISEASE MUTATION / COMPLEX (HYDROLASE-INHIBITOR) / HYDROLASE-HYDROLASE INHIBITOR COMPLEX / BLOOD COAGULATION-HYDROLASE INHIBITOR complex |
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hirudo medicinalis (medicinal leech)
homo sapiens (human)
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