2RG3: Covalent complex structure of elastase

Covalent complex structure of elastase. Determined by X-ray diffraction at 1.8 Å resolution. Released 1 Jul 2008.

Method
X-ray diffraction
Resolution
1.8 Å
Organism
Homo sapiens
Chains
1
Atoms
1,823
Mol. weight
24.33 kDa
Released
1 Jul 2008

Explore 2RG3 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2RG3 contains 7 α-helices and 21 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: 7 helices, 21 β-strands

ElementResiduesLengthSheet
β-strand1711
β-strand20-2122
α-helix22-232
β-strand30-3563
β-strand39-48103
β-strand51-5443
α-helix56-594
α-helix63A-63C3
β-strand65-6843
β-strand7214
β-strand81-90103
β-strand9515
β-strand10015
β-strand104-10853
α-helix120-1223
β-strand135-14062
β-strand14316
β-strand15116
β-strand15414
β-strand156-16382
β-strand181-18442
β-strand18911
β-strand198-20142
β-strand208-21582
α-helix2251
β-strand226-23052
α-helix231-2344
α-helix235-2428

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Leukocyte elastaseAprotein218Homo sapiensP08246 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>2RG3_1 Leukocyte elastase (chains A)
IVGGRRARPHAWPFMVSLQLRGGHFCGATLIAPNFVMSAAHCVANVNVRAVRVVLGAHNL
SRREPTRQVFAVQRIFENGYDPVNLLNDIVILQLNGSATINANVQVAQLPAQGRRLGNGV
QCLAMGWGLLGRNRGIASVLQELNVTVVTSLCRRSNVCTLVRGRQAGVCFGDSGSPLVCN
GLIHGIASFVRGGCASGLYPDAFAPVAQFVNWIDSIIQ

Primary citation

X-ray snapshot of the mechanism of inactivation of human neutrophil elastase by 1,2,5-thiadiazolidin-3-one 1,1-dioxide derivatives. Huang, W., Yamamoto, Y., Li, Y. et al. J Med Chem (2008) 51:2003-2008. DOI 10.1021/jm700966p · PubMed

Other PDB entries of the same protein (UniProt P08246 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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