1SCN: Subtilisin carlsberg

Inactivation of subtilisin carlsberg by N-(tert-butoxycarbonyl-alanyl-prolyl-phenylalanyl)-O-benzol hydroxylamine: formation of covalent enzyme-inhibitor linkage in the form of a carbamate derivative. Determined by X-ray diffraction at 1.9 Å resolution. Released 31 Aug 1994.

Method
X-ray diffraction
Resolution
1.9 Å
Organism
Bacillus licheniformis
Chains
1
Atoms
2,094
Mol. weight
28.03 kDa
Ligands
0EF, CA
Released
31 Aug 1994

Explore 1SCN in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1SCN 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.

Chain E: 11 helices, 16 β-strands

ElementResiduesLengthSheet
α-helix7-104
α-helix13-175
β-strand27-3261
β-strand44-4961
α-helix64-7310
β-strand89-9461
α-helix104-11613
β-strand121-12441
β-strand12812
α-helix133-14412
β-strand148-15251
β-strand15913
β-strand16213
β-strand16712
β-strand175-18061
β-strand18611
β-strand198-20141
β-strand205-20954
β-strand213-21754
α-helix220-23718
α-helix243-25210
α-helix2541
β-strand25511
α-helix2561
α-helix260-2634
β-strand26711
α-helix270-2734

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Subtilisin carlsbergEprotein276Bacillus licheniformisP00780 (AlphaFold model)
Sequence of entity 1 (E), FASTA
>1SCN_1 SUBTILISIN CARLSBERG (chains E)
AQTVPYGIPLIKADKVQAQGFKGANVKVAVLDTGIQASHPDLNVVGGASFVAGEAYNTDG
NGHGTHVAGTVAALDNTTGVLGVAPSVSLYAVKVLNSSGSGSYSGIVSGIEWATTNGMDV
INMSLGGASGSTAMKQAVDNAYARGVVVVAAAGNSGNSGSTNTIGYPAKYDSVIAVGAVD
SNSNRASFSSVGAELEVMAPGAGVYSTYPTNTYATLNGTSMASPHVAGAAALILSKHPNL
SASQVRNRLSSTATYLGSSFYYGKGLINVEAAAQAP

Ligands and cofactors

IDNameFormulaCopies
0EFN-(tert-butoxycarbonyl)-L-alanyl-N-[(1R)-1-(carboxyamino)-2-phenylethyl]-L-prol…C22 H32 N4 O61
CACalcium ionCa2

Water and common crystallization additives (NA) are not listed.

Primary citation

Inactivation of subtilisin Carlsberg by N-((tert-butoxycarbonyl)alanylprolylphenylalanyl)-O-benzolhydroxyl- amine: formation of a covalent enzyme-inhibitor linkage in the form of a carbamate derivative. Steinmetz, A.C., Demuth, H.U., Ringe, D. Biochemistry (1994) 33:10535-10544. DOI 10.1021/bi00200a040 · PubMed

Other PDB entries of the same protein (UniProt P00780 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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