PDB ID: 1OD1
Hetero Atom Contents
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0QS | N~2~-[(2r)-2-benzyl-3-(tert-butylsulfonyl)propanoyl]-N-{(1r)-1-(cyclohexylmethyl)-3,3-difluoro-2,2-dihydroxy-4-[(2-morpholin-4-ylethyl)amino]-4-oxobutyl}-3-(1h-imidazol-3-ium-4-yl)-L-alaninamide | PoSSuM | |||
SO4 | Sulfate ion | PoSSuM |
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Download interaction data: 1OD1
Structure summary
Code : | 1OD1 PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE INHIBITOR | ||||||||||||
Title : | Endothiapepsin PD135,040 complex | ||||||||||||
Release Data : | 2003-06-12 | ||||||||||||
Compound : |
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Authors : | Coates, L., Erskine, P.T., Mall, S., Gill, R.S., Wood, S.P., Cooper, J.B. | ||||||||||||
Keywords : | ACID PROTEINASE, INHIBITOR, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.37 Å ) | ||||||||||||
Citation : |
The Structure of Endothiapepsin Complexed with the Gem-Diol Inhibitor Pd-135,040 at 1.37 A
Coates, L.,Erskine, P.T.,Mall, S.
et al.
PubMed: 12777758 |
Reaction
Chain : | A | ||||||||
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UniProt : | P11838 (CARP_CRYPA) | ||||||||
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