4Z2A image
Deposition Date 2015-03-29
Release Date 2016-05-04
Last Version Date 2026-02-11
Entry Detail
PDB ID:
4Z2A
Keywords:
Title:
Crystal structure of unglycosylated apo human furin @1.89A
Biological Source:
Source Organism(s):
Homo sapiens (Taxon ID: 9606)
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.89 Å
R-Value Free:
0.18
R-Value Work:
0.14
R-Value Observed:
0.14
Space Group:
C 1 2 1
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Furin
Gene (Uniprot):FURIN
Mutagens:N387D, N440D
Chain IDs:A
Chain Length:465
Number of Molecules:1
Biological Source:Homo sapiens
Primary Citation
BacMam production and crystal structure of nonglycosylated apo human furin at 1.89 angstrom resolution.
Acta Crystallogr.,Sect.F 75 239 245 (2019)
PMID: 30950824 DOI: 10.1107/S2053230X19001419

Abstact

Furin, also called proprotein convertase subtilisin/kexin 3 (PCSK3), is a calcium-dependent serine endoprotease that processes a wide variety of proproteins involved in cell function and homeostasis. Dysregulation of furin has been implicated in numerous disease states, including cancer and fibrosis. Mammalian cell expression of the furin ectodomain typically produces a highly glycosylated, heterogeneous protein, which can make crystallographic studies difficult. Here, the expression and purification of nonglycosylated human furin using the BacMam technology and site-directed mutagenesis of the glycosylation sites is reported. Nonglycosylated furin produced using this system retains full proteolytic activity indistinguishable from that of the glycosylated protein. Importantly, the nonglycosylated furin protein reliably forms extremely durable apo crystals that diffract to high resolution. These crystals can be soaked with a wide variety of inhibitors to enable a structure-guided drug-discovery campaign.

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Primary Citation of related structures
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