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Ligands
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Non-standard Residues
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9E7 N~6~-(sulfanylmethyl)-L-lysine
Glycosylation
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Modification
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ACE Acetyl group
NH2 Amino group
Code : 5VK1   PDBj   RCSB PDB   PDBe
Header : SIGNALING PROTEIN/INHIBITOR
Title : Crystal structure of human MDM4 in complex with a 12-mer lysine-cysteine side chain dithiocarbamate stapled peptide inhibitor PMI
Release Data : 2018-04-25
Compound :
mol_id molecule chains synonym
1 Protein Mdm4 A,C,E,G,I,K,M,O Double minute 4 protein,Mdm2-like p53-binding protein,Protein Mdmx,p53-binding protein Mdm4
fragment: residues 24-108
mutation: Q68A, Q69A, E70A
mol_id molecule chains
2 Lysine-cysteine side chain dithiocarbamate stapled peptide inhibitor PMI B,D,F,H,J,L,N,P
Source :
mol_id organism_scientific organism_common
1 Homo sapiens  (taxid:9606) Human
synthetic: yes
mol_id organism_scientific
2 Synthetic construct  (taxid:32630)
synthetic: yes
Authors : Tolbert, W.D., Gohain, N., Pazgier, M.
Keywords : MDMX, MDMX-PEPTIDE INHIBITOR COMPLEX, ONCOPROTEIN, METAL-BINDING, NUCLEUS, ZINC-FINGER, stapled peptide, SIGNALING PROTEIN-INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 2.69 Å )
Citation :

Dithiocarbamate-inspired side chain stapling chemistry for peptide drug design.

Li, X.,Tolbert, W.D.,Hu, H.G.  et al.
(2019)  Chem Sci  10 : 1522 - 1530

PubMed: 30809370
DOI: 10.1039/c8sc03275k

Chain : A, C, E, G, I, K, M, O
UniProt : O15151 (MDM4_HUMAN)
Reaction : -