Trans-cinnamoyl-subtilisin in anhydrous acetonitrile. Determined by X-ray diffraction at 2.15 Å resolution. Released 14 Oct 1998.
Explore 1BE6 in 3D Show helices and sheets RCSB PDB PDBe
1BE6 contains 11 α-helices and 16 β-strands across 1 chain. 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 | 2 | 1 | 1 |
| α-helix | 7-10 | 4 | |
| α-helix | 13-17 | 5 | |
| β-strand | 27-32 | 6 | 2 |
| β-strand | 44-49 | 6 | 2 |
| α-helix | 64-73 | 10 | |
| β-strand | 80 | 1 | 1 |
| β-strand | 89-94 | 6 | 2 |
| α-helix | 104-116 | 13 | |
| β-strand | 121-124 | 4 | 2 |
| β-strand | 128 | 1 | 3 |
| α-helix | 133-144 | 12 | |
| β-strand | 148-152 | 5 | 2 |
| β-strand | 167 | 1 | 3 |
| β-strand | 175-180 | 6 | 2 |
| α-helix | 185 | 1 | |
| β-strand | 186 | 1 | 2 |
| α-helix | 187 | 1 | |
| β-strand | 196-201 | 6 | 2 |
| β-strand | 205-209 | 5 | 4 |
| β-strand | 213-217 | 5 | 4 |
| α-helix | 220-237 | 18 | |
| α-helix | 243-252 | 10 | |
| β-strand | 255 | 1 | 2 |
| α-helix | 260-263 | 4 | |
| β-strand | 267 | 1 | 2 |
| α-helix | 270-273 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Subtilisin carlsberg | A | protein | 274 | Bacillus licheniformis | P00780 (AlphaFold model) |
>1BE6_1 SUBTILISIN CARLSBERG (chains A) AQTVPYGIPLIKADKVQAQGFKGANVKVAVLDTGIQASHPDLNVVGGASFVAGEAYNTDG NGHGTHVAGTVAALDNTTGVLGVAPSVSLYAVKVLNSSGSGSYSGIVSGIEWATTNGMDV INMSLGGASGSTAMKQAVDNAYARGVVVVAAAGNSGNSGSTNTIGYPAKYDSVIAVGAVD SNSNRASFSSVGAELEVMAPGAGVYSTYPTNTYATLNGTSMASPHVAGAAALILSKHPNL SASQVRNRLSSTATYLGSSFYYGKGLINVEAAAQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| CCN | Acetonitrile | C2 H3 N | 12 |
| TCA | Phenylethylenecarboxylic acid | C9 H8 O2 | 1 |
| CA | Calcium ion | Ca | 1 |
Comparison of x-ray crystal structures of an acyl-enzyme intermediate of subtilisin Carlsberg formed in anhydrous acetonitrile and in water. Schmitke, J.L., Stern, L.J., Klibanov, A.M. Proc Natl Acad Sci U S A (1998) 95:12918-12923. DOI 10.1073/pnas.95.22.12918 · PubMed
Other PDB entries of the same protein (UniProt P00780 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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