Brand  (β version)

  The number of atoms exceeds 100,000.
  So, it can not be displayed here.

Select unit:

Select hetatm:   

close
information
centroid:
interaction residue:

Select chain:   Sequence  

Data format:   

Color scheme of protein:

Ligands
Code Name Style Show Link
DMS Dimethyl sulfoxide
EDO 1,2-ethanediol
FNV 4-methyl-1-{[(2r)-5-oxomorpholin-2-yl]methyl}-5-[(4-{[6-(2,2,2-trifluoroethyl)thieno[2,3-D]pyrimidin-4-yl]amino}piperidin-1-yl)methyl]-1h-indole-2-carbonitrile
PG4 Tetraethylene glycol
SO4 Sulfate ion
Non-standard Residues
Code Name Show
Glycosylation
Code Name Emphasize
Modification
Code Name Show
Code : 6BY8   PDBj   RCSB PDB   PDBe
Header : PROTEIN BINDING
Title : Menin in complex with MI-1482
Release Data : 2018-11-28
Compound :
mol_id molecule chains
1 Menin A
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: MEN1, SCG2
Authors : Borkin, T., Klossowski, S., Pollock, J., Linhares, B., Cierpicki, T., Grembecka, J.
Keywords : Protein binding, inhibitor
Exp. method : X-RAY DIFFRACTION ( 1.9 Å )
Citation :

Complexity of Blocking Bivalent Protein-Protein Interactions: Development of a Highly Potent Inhibitor of the Menin-Mixed-Lineage Leukemia Interaction.

Borkin, D.,Klossowski, S.,Pollock, J.  et al.
(2018)  J.Med.Chem.  61 : 4832 - 4850

PubMed: 29738674
DOI: 10.1021/acs.jmedchem.8b00071

Chain : A
UniProt : O00255 (MEN1_HUMAN)
Reaction : -