5QUA: Swapped human Nck SH3.1 domain, 1.5A, C2221

Crystal Structure of swapped human Nck SH3.1 domain, 1.5A, C2221. Determined by X-ray diffraction at 1.51 Å resolution. Released 12 Feb 2020.

Method
X-ray diffraction
Resolution
1.51 Å
Organism
Homo sapiens
Chains
2
Atoms
1,016
Mol. weight
20.6 kDa
Released
12 Feb 2020

Explore 5QUA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5QUA contains 3 α-helices and 15 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: 2 helices, 7 β-strands

ElementResiduesLengthSheet
β-strand4-741
β-strand1112
α-helix19-202
β-strand2112
β-strand26-2941
β-strand36-4051
β-strand46-5051
α-helix51-533
β-strand54-5521
Chain B: 1 helix, 8 β-strands
ElementResiduesLengthSheet
β-strand3-751
β-strand1113
β-strand1811
β-strand2113
β-strand26-2941
β-strand36-4051
β-strand46-5051
α-helix51-533
β-strand54-5521

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Cytoplasmic protein NCK1A, Bprotein87Homo sapiensP16333 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5QUA_1 Cytoplasmic protein NCK1 (chains A, B)
SGGLNDIFEAQKIEWHEGSENLYFQSMAEEVVVVAKFDYVAQQEQELDIKKNERLWLLDD
SKSWWRVRNSMNKTGFVPSNYVERKNS

Primary citation

Small molecule AX-024 reduces T cell proliferation independently of CD3ε/Nck1 interaction, which is governed by a domain swap in the Nck1-SH3.1 domain. Richter, K., Rufer, A.C., Muller, M. et al. J Biol Chem (2020) 295:7849-7864. DOI 10.1074/jbc.RA120.012788 · PubMed

Other PDB entries of the same protein (UniProt P16333 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

About this viewer

MolViewer shows 5QUA directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.