2LNK: Ca-bound S100A4

Solution structure of Ca-bound S100A4 in complex with non-muscle myosin IIA. Determined by solution NMR. Released 25 Apr 2012.

Method
Solution NMR
Organism
Homo sapiens
Chains
3
Atoms
1,952
Mol. weight
30.81 kDa
Released
25 Apr 2012

Explore 2LNK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2LNK contains 13 α-helices and 4 β-strands across 3 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: 5 helices, 2 β-strands

ElementResiduesLengthSheet
α-helix4-1815
β-strand2911
α-helix31-4111
α-helix43-464
α-helix54-629
β-strand7011
α-helix72-8817
Chain B: 6 helices, 2 β-strands
ElementResiduesLengthSheet
α-helix4-1815
β-strand29-3022
α-helix31-4111
α-helix44-463
α-helix52-6110
β-strand69-7022
α-helix72-8615
α-helix87-926
Chain C: 2 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix1899-19035
α-helix1905-192117

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Myosin heavy chain, non-muscle IIaCprotein39Homo sapiensP35579 (AlphaFold model)
Protein S100-A4A, Bprotein113Homo sapiensP26447 (AlphaFold model)
Sequence of entity 1 (C), FASTA
>2LNK_1 Myosin heavy chain, non-muscle IIa (chains C)
QRELEDATETADAMNREVSSLKNKLRRGDLPFVVPRRMA
Sequence of entity 2 (A, B), FASTA
>2LNK_2 Protein S100-A4 (chains A, B)
MRGSHHHHHHGSMACPLEKALDVMVSTFHKYSGKEGDKFKLNKSELKELLTRELPSFLGK
RTDEAAFQKLMSNLDSNRDNEVDFQEYCVFLSCIAMMCNEFFEGFPDKQPRKK

Primary citation

Asymmetric Mode of Ca(2+)-S100A4 Interaction with Nonmuscle Myosin IIA Generates Nanomolar Affinity Required for Filament Remodeling. Elliott, P.R., Irvine, A.F., Jung, H.S. et al. Structure (2012) 20:654-666. DOI 10.1016/j.str.2012.02.002 · PubMed

Other PDB entries of the same protein (UniProt P35579 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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