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TargetCapsid scaffolding protein
LigandBDBM50133954
Substrate/Competitorn/a
Meas. Tech.ChEMBL_158964 (CHEMBL769610)
Ki 79±n/a nM
Citation Borthwick, ADDavies, DEErtl, PFExall, AMHaley, TMHart, GJJackson, DLParry, NRPatikis, ATrivedi, NWeingarten, GGWoolven, JM Design and synthesis of pyrrolidine-5,5'-trans-lactams (5-oxo-hexahydropyrrolo[3,2-b]pyrroles) as novel mechanism-based inhibitors of human cytomegalovirus protease. 4. Antiviral activity and plasma stability. J Med Chem46:4428-49 (2003) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Capsid scaffolding protein
Name:Capsid scaffolding protein
Synonyms:APNG | Assemblin | Assembly protein | Capsid protein P40 | Human cytomegalovirus protease (HCMV Pr) | Human herpes virus 5 capsid protein P40 | Protease precursor | SCAF_HCMVA | UL80 | pPR
Type:PROTEIN
Mol. Mass.:73854.16
Organism:Human cytomegalovirus (strain AD169) (HHV-5) (Human herpesvirus 5)
Description:ChEMBL_158958
Residue:708
Sequence:
MTMDEQQSQAVAPVYVGGFLARYDQSPDEAELLLPRDVVEHWLHAQGQGQPSLSVALPLN
INHDDTAVVGHVAAMQSVRDGLFCLGCVTSPRFLEIVRRASEKSELVSRGPVSPLQPDKV
VEFLSGSYAGLSLSSRRCDDVEAATSLSGSETTPFKHVALCSVGRRRGTLAVYGRDPEWV
TQRFPDLTAADRDGLRAQWQRCGSTAVDASGDPFRSDSYGLLGNSVDALYIRERLPKLRY
DKQLVGVTERESYVKASVSPEAACDIKAASAERSGDSRSQAATPAAGARVPSSSPSPPVE
PPSPVQPPALPASPSVLPAESPPSLSPSEPAEAASMSHPLSAAVPAATAPPGATVAGASP
AVSSLAWPHDGVYLPKDAFFSLLGASRSAVPVMYPGAVAAPPSASPAPLPLPSYPASYGA
PVVGYDQLAARHFADYVDPHYPGWGRRYEPAPSLHPSYPVPPPPSPAYYRRRDSPGGMDE
PPSGWERYDGGHRGQSQKQHRHGGSGGHNKRRKETAAASSSSSDEDLSFPGEAEHGRARK
RLKSHVNSDGGSGGHAGSNQQQQQRYDELRDAIHELKRDLFAARQSSTLLSAALPSAASS
SPTTTTVCTPTGELTSGGGETPTALLSGGAKVAERAQAGVVNASCRLATASGSEAATAGP
STAGSSSCPASVVLAAAAAQAAAASQSPPKDMVDLNRRIFVAALNKLE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50133954
n/a
NameBDBM50133954
Synonyms:(3S,3aR,6aS)-1-Cyclopropanecarbonyl-3-methyl-4-[(S)-1-(4-propoxy-benzoyl)-pyrrolidine-2-carbonyl]-hexahydro-pyrrolo[3,2-b]pyrrol-2-one | CHEMBL138211
TypeSmall organic molecule
Emp. Form.C26H33N3O5
Mol. Mass.467.5573
SMILESCCCOc1ccc(cc1)C(=O)N1CCC[C@H]1C(=O)N1CC[C@H]2[C@H]1[C@H](C)C(=O)N2C(=O)C1CC1
Structure
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