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Structure paper

TitleStructure-based design of covalent siah inhibitors.
Journal, issue, pagesChem. Biol., Vol. 20, Page 973-982, Year 2013
Publish dateNov 30, 2012 (structure data deposition date)
AuthorsStebbins, J.L. / Santelli, E. / Feng, Y. / De, S.K. / Purves, A. / Motamedchaboki, K. / Wu, B. / Ronai, Z.A. / Liddington, R.C. / Pellecchia, M.
External linksChem. Biol. / PubMed:23891150
MethodsX-ray diffraction
Resolution2.4 - 3 Å
Structure data

PDB-4i7b:
Siah1 bound to synthetic peptide (ACE)KLRPV(ABA)MVRPTVR
Method: X-RAY DIFFRACTION / Resolution: 3 Å

PDB-4i7c:
Siah1 mutant bound to synthetic peptide (ACE)KLRPV(23P)MVRPWVR
Method: X-RAY DIFFRACTION / Resolution: 2.8 Å

PDB-4i7d:
Siah1 bound to synthetic peptide (ACE)KLRPVAMVRP(PRK)VR
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-HOH:
WATER

ChemComp-MPD:
(4S)-2-METHYL-2,4-PENTANEDIOL / precipitant*YM

Source
  • homo sapiens (human)
  • drosophila melanogaster (fruit fly)
KeywordsLIGASE/LIGASE INHIBITOR / Sina / beta sandwich / zinc finger / ubiquitin ligase / LIGASE-LIGASE INHIBITOR complex / covalent inhibitor

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