Solution structure of human Ca2+-loaded S100A4 cys-free mutant. Determined by solution NMR. Released 8 Jul 2015.
Explore 2MRD in 3D Show helices and sheets RCSB PDB PDBe
2MRD contains 8 α-helices and 4 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 4-20 | 17 | |
| β-strand | 28-30 | 3 | 1 |
| α-helix | 31-41 | 11 | |
| α-helix | 52-62 | 11 | |
| β-strand | 69-71 | 3 | 1 |
| α-helix | 72-88 | 17 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Protein S100-A4 | A, B | protein | 101 | Homo sapiens | P26447 (AlphaFold model) |
>2MRD_1 Protein S100-A4 (chains A, B) MASPLEKALDVMVSTFHKYSGKEGDKFKLNKSELKELLTRELPSFLGKRTDEAAFQKLMS NLDSNRDNEVDFQEYSVFLSSIAMMSNEFFEGFPDKQPRKK
The solution structure of human calcium-bound S100A4 mutated at four cysteine loci. Cho, C.C., Hung, K.W., Gorja, D.R. et al. J Biomol NMR (2015) 62:233-238. DOI 10.1007/s10858-015-9927-6 · PubMed
Other PDB entries of the same protein (UniProt P26447 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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