6YIB: 14-3-3 sigma

14-3-3 sigma in complex with SMAD3 pS423 peptide. Determined by X-ray diffraction at 1.7 Å resolution. Released 14 Apr 2021.

Method
X-ray diffraction
Resolution
1.7 Å
Organism
Homo sapiens
Chains
2
Atoms
2,387
Mol. weight
28.11 kDa
Ligands
MG, CA
Released
14 Apr 2021

Explore 6YIB in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6YIB contains 15 α-helices and 0 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 14 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix3-1513
α-helix19-3012
α-helix35-373
α-helix38-6932
α-helix80-10223
α-helix103-1075
α-helix108-1103
α-helix114-13421
α-helix140-16122
α-helix167-17812
α-helix179-1835
α-helix187-20216
α-helix205-2073
α-helix210-23021
Chain P: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix124-1263

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
14-3-3 protein sigmaAprotein236Homo sapiensP31947 (AlphaFold model)
SMAD3Pprotein11Homo sapiensP84022 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6YIB_1 14-3-3 protein sigma (chains A)
GAMGSMERASLIQKAKLAEQAERYEDMAAFMKGAVEKGEELSCEERNLLSVAYKNVVGGQ
RAAWRVLSSIEQKSNEEGSEEKGPEVREYREKVETELQGVCDTVLGLLDSHLIKEAGDAE
SRVFYLKMKGDYYRYLAEVATGDDKKRIIDSARSAYQEAMDISKKEMPPTNPIRLGLALN
FSVFHYEIANSPEEAISLAKTTFDEAMADLHTLSEDSYKDSTLIMQLLRDNLTLWT
Sequence of entity 2 (P), FASTA
>6YIB_2 SMAD3 (chains P)
XWPSIRCSSVS

Ligands and cofactors

IDNameFormulaCopies
MGMagnesium ionMg3
CACalcium ionCa1

Water and common crystallization additives (NA, GOL, CL) are not listed.

Primary citation

Identification and characterization of 14-3-3/SMAD protein-protein-interactions. Graf, S., Kiehstaller, S., Ottmann, C. et al. To be published.

Other PDB entries of the same protein (UniProt P31947 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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