5MAE: CATHEPSIN L

CATHEPSIN L IN COMPLEX WITH (2S,4R)-4-(2-Chloro-4-methoxy-benzenesulfonyl)-1-[3-(5-chloro-pyridin-2-yl)-azetidine-3-carbonyl]-pyrrolidine-2-car boxylic acid (1-cyano-cyclopropyl)-amide. Determined by X-ray diffraction at 1.0 Å resolution. Released 11 Jan 2017.

Method
X-ray diffraction
Resolution
1.0 Å
Organism
Homo sapiens
Chains
1
Atoms
2,154
Mol. weight
24.81 kDa
Ligands
7KN
Released
11 Jan 2017

Explore 5MAE in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5MAE contains 11 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: 11 helices, 17 β-strands

ElementResiduesLengthSheet
β-strand5-621
α-helix7-104
α-helix14-163
β-strand1812
β-strand2313
α-helix25-4218
β-strand4814
α-helix50-567
α-helix58-603
β-strand6613
α-helix70-8011
β-strand83-8425
β-strand8514
α-helix102-1043
β-strand105-10735
β-strand111-11441
α-helix115-1162
α-helix119-12911
β-strand132-13651
α-helix141-1444
β-strand150-15121
β-strand163-173111
β-strand180-18671
β-strand18912
β-strand19511
β-strand198-20251
α-helix208-2103
β-strand216-21941

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Cathepsin L1Aprotein220Homo sapiensP07711 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5MAE_1 Cathepsin L1 (chains A)
APRSVDWREKGYVTPVKNQGQCGSCWAFSATGALEGQMFRKTGRLISLSEQNLVDCSGPQ
GNEGCNGGLMDYAFQYVQDNGGLDSEESYPYEATEESCKYNPKYSVANDTGFVDIPKQEK
ALMKAVATVGPISVAIDAGHESFLFYKEGIYFEPDCSSEDMDHGVLVVGYGFESTESDNN
KYWLVKNSWGEEWGMGGYVKMAKDRRNHCGIASAASYPTV

Ligands and cofactors

IDNameFormulaCopies
7KN[4-[cyclopentyl(pyrazin-2-ylmethyl)amino]-6-morpholin-4-yl-1,3,5-triazin-2-yl]m…C18 H23 N8 O1

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

Primary citation

Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: AmideHeteroarene pi-Stacking Interactions and Chalcogen Bonding in the S3 Pocket. Giroud, M., Ivkovic, J., Martignoni, M. et al. ChemMedChem (2017) 12:257-270. DOI 10.1002/cmdc.201600563 · PubMed

Other PDB entries of the same protein (UniProt P07711 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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