5WXO

Crystal structure of uPA in complex with upain-2-2-W3A

Summary for 5WXO

• Entry DOI: 10.2210/pdb5wxo/pdb
• Related: 5WXF 5WXP 5WXQ 5WXR 5WXS 5WXT
• Descriptor: Urokinase-type plasminogen activator chain B, upain-2-2-W3A peptide (3 entities in total)
• Functional Keywords: serine proteases, upa, pepetide inhibitors, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 2
• Total formula weight: 29688.77

Authors

Jiang, L.,Huang, M. (deposition date: 2017-01-08, release date: 2018-07-11, Last modification date: 2023-11-22)

Primary citation

Jiang, L.,Oldenburg, E.,Kromann-Hansen, T.,Xu, P.,Jensen, J.K.,Andreasen, P.A.,Huang, M.
Cleavage of peptidic inhibitors by target protease is caused by peptide conformational transition.
Biochim. Biophys. Acta, 1862:2017-2023, 2018

PubMed Abstract: Some peptide sequences can behave as either substrates or inhibitors of serine proteases. Working with a cyclic peptidic inhibitor of the serine protease urokinase-type plasminogen activator (uPA), we have now demonstrated a new mechanism for an inhibitor-to-substrate switch. The peptide, CSWRGLENHAAC (upain-2), is a competitive inhibitor of human uPA, but is also slowly converted to a substrate in which the bond between Arg and Gly (the P1-P1' bond) is cleaved. Substituting the P2 residue Trp to an Ala or substituting the P1 Arg residue with 4-guanidino-phenylalanine strongly increased the substrate cleavage rate. We studied the structural basis for the inhibitor-to-substrate switch by determining the crystal structures of the various peptide variants in complex with the catalytic domain of uPA. While the slowly cleaved peptides bound clearly in inhibitory mode, with the oxyanion hole blocked by the side chain of the P3' residue Glu, peptides behaving essentially as substrates with a much accelerated rate of cleavage was observed to be bound to the enzyme in substrate mode. Our analysis reveals that the inhibitor-to-substrate switch was associated with a 7 Å translocation of the P2 residue, and we conclude that the inhibitor-to-substrate switch of upain-2 is a result of a major conformational change in the enzyme-bound state of the peptide. This conclusion is in contrast to findings with so-called standard mechanism inhibitors in which the inhibitor-to-substrate switch is linked to minor conformational changes in the backbone of the inhibitory peptide stretch.

PubMed: 29959058
DOI: 10.1016/j.bbagen.2018.06.016

Experimental method

X-RAY DIFFRACTION (1.64 Å)