Solution structure of Ca-bound S100A4 in complex with non-muscle myosin IIA. Determined by solution NMR. Released 25 Apr 2012.
Explore 2LNK in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-18 | 15 | |
| β-strand | 29 | 1 | 1 |
| α-helix | 31-41 | 11 | |
| α-helix | 43-46 | 4 | |
| α-helix | 54-62 | 9 | |
| β-strand | 70 | 1 | 1 |
| α-helix | 72-88 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-18 | 15 | |
| β-strand | 29-30 | 2 | 2 |
| α-helix | 31-41 | 11 | |
| α-helix | 44-46 | 3 | |
| α-helix | 52-61 | 10 | |
| β-strand | 69-70 | 2 | 2 |
| α-helix | 72-86 | 15 | |
| α-helix | 87-92 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1899-1903 | 5 | |
| α-helix | 1905-1921 | 17 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Myosin heavy chain, non-muscle IIa | C | protein | 39 | Homo sapiens | P35579 (AlphaFold model) |
| Protein S100-A4 | A, B | protein | 113 | Homo sapiens | P26447 (AlphaFold model) |
>2LNK_1 Myosin heavy chain, non-muscle IIa (chains C) QRELEDATETADAMNREVSSLKNKLRRGDLPFVVPRRMA
>2LNK_2 Protein S100-A4 (chains A, B) MRGSHHHHHHGSMACPLEKALDVMVSTFHKYSGKEGDKFKLNKSELKELLTRELPSFLGK RTDEAAFQKLMSNLDSNRDNEVDFQEYCVFLSCIAMMCNEFFEGFPDKQPRKK
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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