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PDBsum entry 7fqh

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protein ligands Protein-protein interface(s) links
Hydrolase/inhibitor PDB id
7fqh

 

 

 

 

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Contents
Protein chains
262 a.a.
Ligands
WR9 ×3
EDO ×2
NAG ×2
Waters ×88
PDB id:
7fqh
Name: Hydrolase/inhibitor
Title: Crystal structure of human legumain in complex with (2s)-n-[(3s)-5- amino-5-oxopent-1-yn-3-yl]-1-[1-[4-(cyclopropylmethoxy) phenyl]cyclopropanecarbonyl]pyrrolidine-2-carboxamide
Structure: Legumain. Chain: a, b, d. Synonym: asparaginyl endopeptidase,protease,cysteine 1. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: lgmn, prsc1. Expressed in: drosophila melanogaster. Expression_system_taxid: 7215.
Resolution:
2.18Å     R-factor:   0.226     R-free:   0.272
Authors: A.Ehler,J.Benz,B.Bartels,S.Hewings-David,M.G.Rudolph
Key ref: B.Bartels et al. Crystal structure of a human legumain complex. To be published, .
Date:
05-Oct-22     Release date:   11-Oct-23    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q99538  (LGMN_HUMAN) -  Legumain from Homo sapiens
Seq:
Struc:
433 a.a.
262 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 2 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: E.C.3.4.22.34  - legumain.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Hydrolysis of proteins and small-molecule substrates at -Asn-|-Xaa- bonds.

 

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