Human mesotrypsin-S39Y complexed with bovine pancreatic trypsin inhibitor (BPTI). Determined by X-ray diffraction at 1.4 Å resolution. Released 12 Sept 2012.
Explore 4DG4 in 3D Show helices and sheets RCSB PDB PDBe
4DG4 contains 44 α-helices and 100 β-strands across 8 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 | 17 | 1 | 1 |
| β-strand | 20-21 | 2 | 2 |
| α-helix | 22-23 | 2 | |
| β-strand | 30-34 | 5 | 3 |
| β-strand | 40-46 | 7 | 3 |
| β-strand | 51-54 | 4 | 3 |
| α-helix | 56-58 | 3 | |
| β-strand | 64-67 | 4 | 3 |
| β-strand | 72 | 1 | 4 |
| β-strand | 75 | 1 | 4 |
| β-strand | 81-90 | 10 | 3 |
| β-strand | 104-108 | 5 | 3 |
| α-helix | 111-114 | 4 | |
| β-strand | 122 | 1 | 2 |
| α-helix | 123-124 | 2 | |
| β-strand | 135-140 | 6 | 2 |
| β-strand | 146 | 1 | 5 |
| β-strand | 148 | 1 | 5 |
| β-strand | 154 | 1 | 4 |
| β-strand | 156-162 | 7 | 2 |
| α-helix | 163-164 | 2 | |
| α-helix | 165-171 | 7 | |
| β-strand | 180-183 | 4 | 2 |
| β-strand | 189 | 1 | 1 |
| β-strand | 198-201 | 4 | 2 |
| β-strand | 204-215 | 8 | 2 |
| β-strand | 226-230 | 5 | 2 |
| α-helix | 231-234 | 4 | |
| α-helix | 235-244 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 17 | 1 | 7 |
| β-strand | 20-21 | 2 | 8 |
| α-helix | 22-23 | 2 | |
| β-strand | 30-34 | 5 | 9 |
| β-strand | 40-48 | 9 | 9 |
| β-strand | 51-54 | 4 | 9 |
| α-helix | 56-58 | 3 | |
| β-strand | 64-67 | 4 | 9 |
| β-strand | 72 | 1 | 10 |
| β-strand | 75 | 1 | 10 |
| β-strand | 81-90 | 10 | 9 |
| β-strand | 104-108 | 5 | 9 |
| α-helix | 111-114 | 4 | |
| β-strand | 122 | 1 | 8 |
| α-helix | 123-124 | 2 | |
| α-helix | 128-130 | 3 | |
| β-strand | 135-140 | 6 | 8 |
| β-strand | 146 | 1 | 11 |
| β-strand | 148 | 1 | 11 |
| β-strand | 154 | 1 | 10 |
| β-strand | 156-162 | 7 | 8 |
| α-helix | 163-164 | 2 | |
| α-helix | 165-171 | 7 | |
| β-strand | 180-183 | 4 | 8 |
| β-strand | 189 | 1 | 7 |
| β-strand | 198-201 | 4 | 8 |
| β-strand | 204-215 | 8 | 8 |
| β-strand | 226-230 | 5 | 8 |
| α-helix | 231-234 | 4 | |
| α-helix | 235-244 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3-6 | 4 | |
| α-helix | 8-9 | 2 | |
| β-strand | 14 | 1 | 8 |
| β-strand | 18-24 | 7 | 12 |
| β-strand | 29-35 | 7 | 12 |
| β-strand | 45 | 1 | 12 |
| α-helix | 48-55 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 17 | 1 | 13 |
| β-strand | 20-21 | 2 | 14 |
| α-helix | 22-23 | 2 | |
| β-strand | 30-34 | 5 | 15 |
| β-strand | 40-46 | 7 | 15 |
| β-strand | 51-54 | 4 | 15 |
| α-helix | 56-58 | 3 | |
| β-strand | 64-67 | 4 | 15 |
| β-strand | 72 | 1 | 16 |
| β-strand | 75 | 1 | 10 |
| β-strand | 81-90 | 10 | 15 |
| β-strand | 104-108 | 5 | 15 |
| β-strand | 122 | 1 | 14 |
| α-helix | 123-124 | 2 | |
| β-strand | 135-140 | 6 | 14 |
| β-strand | 146 | 1 | 17 |
| β-strand | 148 | 1 | 17 |
| β-strand | 154 | 1 | 16 |
| β-strand | 156-162 | 7 | 14 |
| α-helix | 163-164 | 2 | |
| α-helix | 165-171 | 7 | |
| β-strand | 180-183 | 4 | 14 |
| β-strand | 189 | 1 | 13 |
| β-strand | 198-201 | 4 | 14 |
| β-strand | 204-215 | 8 | 14 |
| β-strand | 226-230 | 5 | 14 |
| α-helix | 231-234 | 4 | |
| α-helix | 235-244 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 17 | 1 | 19 |
| β-strand | 20-21 | 2 | 20 |
| α-helix | 22-23 | 2 | |
| β-strand | 30-34 | 5 | 21 |
| β-strand | 40-48 | 9 | 21 |
| β-strand | 51-54 | 4 | 21 |
| α-helix | 56-58 | 3 | |
| β-strand | 64-67 | 4 | 21 |
| β-strand | 72 | 1 | 22 |
| β-strand | 75 | 1 | 4 |
| β-strand | 81-90 | 10 | 21 |
| β-strand | 104-108 | 5 | 21 |
| α-helix | 111-114 | 4 | |
| β-strand | 122 | 1 | 20 |
| α-helix | 123-124 | 2 | |
| β-strand | 135-140 | 6 | 20 |
| β-strand | 146 | 1 | 23 |
| β-strand | 148 | 1 | 23 |
| β-strand | 154 | 1 | 22 |
| β-strand | 156-162 | 7 | 20 |
| α-helix | 163-164 | 2 | |
| α-helix | 165-171 | 7 | |
| β-strand | 180-183 | 4 | 20 |
| β-strand | 189 | 1 | 19 |
| β-strand | 198-201 | 4 | 20 |
| β-strand | 204-215 | 8 | 20 |
| β-strand | 226-230 | 5 | 20 |
| α-helix | 231-234 | 4 | |
| α-helix | 235-244 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| PRSS3 protein | A, B, D, G | protein | 224 | Homo sapiens | P35030 (AlphaFold model) |
| Pancreatic trypsin inhibitor | C, E, F, H | protein | 58 | Bos taurus | P00974 (AlphaFold model) |
>4DG4_1 PRSS3 protein (chains A, B, D, G) IVGGYTCEENSLPYQVSLNSGYHFCGGSLISEQWVVSAAHCYKTRIQVRLGEHNIKVLEG NEQFINAAKIIRHPKYNRDTLDNDIMLIKLSSPAVINARVSTISLPTAPPAAGTECLISG WGNTLSFGADYPDELKCLDAPVLTQAECKASYPGKITNSMFCVGFLEGGKDSCQRDAGGP VVCNGQLQGVVSWGHGCAWKNRPGVYTKVYNYVDWIKDTIAANS
>4DG4_2 Pancreatic trypsin inhibitor (chains C, E, F, H) RPDFCLEPPYTGPCKARIIRYFYNAKAGLCQTFVYGGCRAKRNNFKSAEDCMRTCGGA
| ID | Name | Formula | Copies |
|---|---|---|---|
| CA | Calcium ion | Ca | 1 |
Water and common crystallization additives (SO4) are not listed.
Presence versus absence of hydrogen bond donor Tyr-39 influences interactions of cationic trypsin and mesotrypsin with protein protease inhibitors. Salameh, M.A., Soares, A.S., Alloy, A. et al. Protein Sci (2012) 21:1103-1112. DOI 10.1002/pro.2097 · PubMed
Other PDB entries of the same protein (UniProt P35030 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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