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UniProt Q15796

Mothers against decapentaplegic homolog 2 (Q15796)

Mothers against decapentaplegic homolog 2 (UniProt Q15796): 16 experimental structures on GenesisL1, 1 ligand bound, 8 pockets. Binding sites, pockets, druggability and 3D structures in GL1X.

UniProt
Q15796
Protein
Mothers against decapentaplegic homolog 2
Experimental structures
16
Predicted models
0
Ligands
1
Pockets
8 · 1 record with a druggable one

Structures

16 records of Q15796 in the MolNFT archive: 16 experimental, 0 predicted.

EntryTitleMethodChainsLigandsPockets
1DEVCrystal structure of SMAD2 MH2 domain bound to the smad-binding domain of sarax-ray diffractionA, C——
1DEVCrystal structure of SMAD2 MH2 domain bound to the smad-binding domain of sarax-ray diffractionA, C——
1KHXCrystal structure of a phosphorylated Smad2x-ray diffractionA——
1KHXCrystal structure of a phosphorylated SMAD2x-ray diffractionA——
1U7VCrystal Structure of the phosphorylated Smad2/Smad4 heterotrimeric complexx-ray diffractionA, C——
1U7VCrystal structure of the phosphorylated SMAD2/SMAD4 heterotrimeric complexx-ray diffractionA, C——
2LB3Structure of the WW domain of PIN1 in complex with a human phosphorylated Smad3 derived peptidesolution nmrB——
2LB3Structure of the ww domain of PIN1 in complex with a human phosphorylated SMAD3 derived peptidesolution nmrB——
5XODCrystal structure of human SMAD2-ski complexx-ray diffractionA——
5ZOJCrystal structure of human SMAD2-MAN1 complexx-ray diffractionA, B, C—7 (best 0.84)
5ZOJCrystal structure of human SMAD2-MAN1 complexx-ray diffractionA, B, C——
6M64Crystal structure of SMAD2 in complex with cbpx-ray diffractionA, C, E——
6ZVQComplex between SMAD2 MH2 domain and peptide from Ski corepressorx-ray diffractionASO41 (best 0.27)
6ZVQComplex between SMAD2 MH2 domain and peptide from ski corepressorx-ray diffractionASO4—
7CO1Crystal structure of SMAD2 in complex with wild-type cbp———
Q15796AlphaFold monomer V2.0 prediction for mothers against decapentaplegic homolog 2 (Q15796)———

Ligands

  • SO4 · Sulfate ion · in 2 records

Elsewhere

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