6FSM: TCE-treated Thermolysin

Crystal structure of TCE-treated Thermolysin. Determined by X-ray diffraction at 1.39 Å resolution. Released 2 May 2018.

Method
X-ray diffraction
Resolution
1.39 Å
Organism
Geobacillus stearothermophilus
Chains
1
Atoms
2,885
Mol. weight
35.22 kDa
Ligands
LYS, VAL, PO4, CA
Released
2 May 2018

Explore 6FSM in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6FSM contains 13 α-helices and 17 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 A: 13 helices, 17 β-strands

ElementResiduesLengthSheet
β-strand4-1181
β-strand17-2591
β-strand27-2931
β-strand31-3222
β-strand39-4352
β-strand53-5422
β-strand56-5721
β-strand61-6221
α-helix65-673
α-helix68-8821
α-helix98-992
β-strand100-10672
β-strand113-11532
β-strand120-12342
β-strand13013
α-helix133-1353
α-helix137-15014
α-helix159-18022
β-strand187-18824
β-strand19313
β-strand203-20424
α-helix208-2114
α-helix217-2193
α-helix225-2295
α-helix234-24613
β-strand248-25035
β-strand253-25535
α-helix260-27314
α-helix281-29616
α-helix301-31212

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
ThermolysinAprotein316Geobacillus stearothermophilusP43133 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6FSM_1 Thermolysin (chains A)
ITGTSTVGVGRGVLGDQKNINTTYSTYYYLQDNTRGDGIFTYDAKYRTTLPGSLWADADN
QFFASYDAPAVDAHYYAGVTYDYYKNVHNRLSYDGNNAAIRSSVHYSQGYNNAFWNGSEM
VYGDGDGQTFIPLSGGIDVVAHELTHAVTDYTAGLIYQNESGAINEAISDIFGTLVEFYA
NKNPDWEIGEDVYTPGISGDSLRSMSDPAKYGDPDHYSKRYTGTQDNGGVHINSGIINKA
AYLISQGGTHYGVSVVGIGRDKLGKIFYRALTQYLTPTSNFSQLRAAAVQSATDLYGSTS
QEVASVKQAFDAVGVK

Ligands and cofactors

IDNameFormulaCopies
LYSLysineC6 H15 N2 O21
VALValineC5 H11 N O21
PO4Phosphate ionO4 P1
CACalcium ionCa4
ZNZinc ionZn1

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

Primary citation

Improved protein-crystal identification by using 2,2,2-trichloroethanol as a fluorescence enhancer. Pichlo, C., Toelzer, C., Chojnacki, K. et al. Acta Crystallogr F Struct Biol Commun (2018) 74:307-314. DOI 10.1107/S2053230X18005253 · PubMed

Other PDB entries of the same protein (UniProt P43133 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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