PDB ID: 3HIW
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Code | Name | Style | Show | Link | |
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C2X | 9,9'-{(2r,3r,3ar,5s,7ar,9r,10r,10ar,12s,23r,25ar,27r,28r,28ar,30s,32ar,35ar,37s,39ar)-9-(6-amino-9h-purin-9-yl)-34-[(4-amino-5h-pyrrolo[3,2-D]pyrimidin-7-yl)methyl]-5,12,23,30,37-pentahydroxy-3,10,28-trimethoxy-5,12,23,30,37-pentaoxidotetracosahydro-2h,7h,25h-trifuro[3,2-f:3',2'-L:3'',2''-x]pyrrolo[3,4-R][1,3,5,9,11,15,17,21,23,27,29,2,4,10,16,22,28]undecaoxazapentaphosphacyclopentatriacontine-2,27-diyl}bis(2-amino-3,9-dihydro-6h-purin-6-one) | PoSSuM |
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Download interaction data: 3HIW
Structure summary
Code : | 3HIW PDBj RCSB PDB PDBe | ||||||||
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Header : | Hydrolase/Hydrolase inhibitor | ||||||||
Title : | Crystal structure of Saporin-L1 in complex with the cyclic tetranucleotide inhibitor, a transition state analogue | ||||||||
Release Data : | 2009-12-08 | ||||||||
Compound : |
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Authors : | Ho, M., Sturm, M.B., Almo, S.C., Schramm, V.L. | ||||||||
Keywords : | transition state, ribosome inactivating proteins, RIPs, Hydrolase, Plant defense, Protein synthesis inhibitor, Toxin, Hydrolase-Hydrolase inhibitor COMPLEX | ||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.800 Å ) | ||||||||
Citation : |
Transition state analogues in structures of ricin and saporin ribosome-inactivating proteins.
Ho, M.C.,Sturm, M.B.,Almo, S.C.
et al.
PubMed: 19920175 |
Reaction
Chain : | A, B | ||||||||
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UniProt : | Q2QEH4 (Q2QEH4_SAPOF) | ||||||||
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