A BPTI-[5,55] variant with C14GA38I mutations. Determined by X-ray diffraction at 1.38 Å resolution. Released 4 Jul 2018.
Explore 5XX5 in 3D Show helices and sheets RCSB PDB PDBe
5XX5 contains 6 α-helices and 6 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 | 3-6 | 4 | |
| α-helix | 8-9 | 2 | |
| β-strand | 18-24 | 7 | 1 |
| β-strand | 29-35 | 7 | 1 |
| β-strand | 45 | 1 | 1 |
| α-helix | 48-55 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Pancreatic trypsin inhibitor | A, B | protein | 58 | Bos taurus | P00974 (AlphaFold model) |
>5XX5_1 Pancreatic trypsin inhibitor (chains A, B) RPDFCLEPPYTGPGKARIIRYFYNAKAGLAQTFVYGGIRAKRNNFKSAEDALRTCGGA
Hydrophobic surface residues can stabilize a protein through improved water-protein interactions. Islam, M.M., Kobayashi, K., Kidokoro, S.I. et al. FEBS J (2019). DOI 10.1111/febs.14941 · PubMed
Other PDB entries of the same protein (UniProt P00974 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 5XX5 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.