Crystal Structure of Porcine pancreatic trypsin with tripeptide inhibitor, TRE, at pH 7. Determined by X-ray diffraction at 1.8 Å resolution. Released 28 Mar 2018.
Explore 5XWJ in 3D Show helices and sheets RCSB PDB PDBe
5XWJ contains 18 α-helices and 40 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 |
|---|---|---|---|
| β-strand | 10 | 1 | 1 |
| β-strand | 13-14 | 2 | 2 |
| α-helix | 15-16 | 2 | |
| β-strand | 23-27 | 5 | 3 |
| β-strand | 31-39 | 9 | 3 |
| β-strand | 42-45 | 4 | 3 |
| α-helix | 47-49 | 3 | |
| β-strand | 55-58 | 4 | 3 |
| β-strand | 62 | 1 | 4 |
| β-strand | 71-80 | 10 | 3 |
| β-strand | 94-98 | 5 | 3 |
| α-helix | 101-104 | 4 | |
| β-strand | 112 | 1 | 2 |
| α-helix | 113-114 | 2 | |
| α-helix | 117-119 | 3 | |
| β-strand | 123-128 | 6 | 2 |
| β-strand | 142 | 1 | 4 |
| β-strand | 144-150 | 7 | 2 |
| α-helix | 151-152 | 2 | |
| α-helix | 153-159 | 7 | |
| β-strand | 168-171 | 4 | 2 |
| β-strand | 179 | 1 | 1 |
| β-strand | 188-191 | 4 | 2 |
| β-strand | 194-201 | 8 | 2 |
| β-strand | 207 | 1 | 5 |
| β-strand | 210 | 1 | 5 |
| β-strand | 212-216 | 5 | 2 |
| α-helix | 217-219 | 3 | |
| α-helix | 221-230 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Trypsin | A, B | protein | 231 | Sus scrofa | P00761 (AlphaFold model) |
| Acetylated-THR-ARG-GLU Inhibitor | C, D | protein | 4 | Capsicum annuum |
>5XWJ_1 Trypsin (chains A, B) FPTDDDDKIVGGYTCAANSIPYQVSLNSGSHFCGGSLINSQWVVSAAHCYKSRIQVRLGE HNIDVLEGNEQFINAAKIITHPNFNGNTLDNDIMLIKLSSPATLNSRVATVSLPRSCAAA GTECLISGWGNTKSSGSSYPSLLQCLKAPVLSDSSCKSSYPGQITGNMICVGFLEGGKDS CQGDSGGPVVCNGQLQGIVSWGYGCAQKNKPGVYTKVCNYVNWIQQTIAAN
>5XWJ_2 Acetylated-THR-ARG-GLU Inhibitor (chains C, D) XTRE
| ID | Name | Formula | Copies |
|---|---|---|---|
| CA | Calcium ion | Ca | 2 |
Water and common crystallization additives (MPD) are not listed.
Tripeptides derived from reactive centre loop of potato type II protease inhibitors preferentially inhibit midgut proteases of Helicoverpa armigera. Saikhedkar, N.S., Joshi, R.S., Bhoite, A.S. et al. Insect Biochem Mol Biol (2018) 95:17-25. DOI 10.1016/j.ibmb.2018.02.001 · PubMed
Other PDB entries of the same protein (UniProt P00761 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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