7B9T: 14-3-3 protein sigma

Cys-45-tethered stabilizer 5 of 14-3-3(sigma)/ERa PPI. Determined by X-ray diffraction at 1.15 Å resolution. Released 7 Jul 2021.

Method
X-ray diffraction
Resolution
1.15 Å
Organism
Homo sapiens
Chains
2
Atoms
2,370
Mol. weight
27.79 kDa
Ligands
T4Z, MG
Released
7 Jul 2021

Explore 7B9T in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7B9T contains 15 α-helices and 0 β-strands across 1 chain. 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: 15 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix3-1513
α-helix19-3113
α-helix35-373
α-helix38-6932
α-helix74-763
α-helix80-10223
α-helix103-1075
α-helix108-1103
α-helix114-13421
α-helix140-16122
α-helix167-17812
α-helix179-1835
α-helix187-20418
α-helix205-2073
α-helix210-23021

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
14-3-3 protein sigmaAprotein236Homo sapiensP31947 (AlphaFold model)
Estrogen receptorBprotein8Homo sapiensP03372 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>7B9T_1 14-3-3 protein sigma (chains A)
GAMGSMERASLIQKAKLAEQAERYEDMAAFMKGAVEKGEELSNEERNLLCVAYKNVVGGQ
RAAWRVLSSIEQKSNEEGSEEKGPEVREYREKVETELQGVCDTVLGLLDSHLIKEAGDAE
SRVFYLKMKGDYYRYLAEVATGDDKKRIIDSARSAYQEAMDISKKEMPPTNPIRLGLALN
FSVFHYEIANSPEEAISLAKTTFDEAMADLHTLSEDSYKDSTLIMQLLRDNLTLWT
Sequence of entity 2 (B), FASTA
>7B9T_2 Estrogen receptor (chains B)
AEGFPATV

Ligands and cofactors

IDNameFormulaCopies
T4Z2-(4-chlorophenyl)sulfanyl-~{N}-(3-sulfanylpropyl)ethanamideC11 H14 Cl N O S21
MGMagnesium ionMg3

Primary citation

Exploration of a 14-3-3 PPI Pocket by Covalent Fragments as Stabilizers. Sijbesma, E., Hallenbeck, K.K., Andrei, S.A. et al. ACS Med Chem Lett (2021) 12:976-982. DOI 10.1021/acsmedchemlett.1c00088 · PubMed

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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