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PDBsum entry 5swl

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protein ligands Protein-protein interface(s) links
Hydrolase PDB id
5swl

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
336 a.a.
Ligands
SO4 ×2
Waters ×106
PDB id:
5swl
Name: Hydrolase
Title: Crystal structure of atpase delta1-79 spa47 e188a
Structure: Probable atp synthase spal/mxib. Chain: a, b. Fragment: unp residues 80-430. Synonym: spa47. Engineered: yes. Mutation: yes
Source: Shigella flexneri. Organism_taxid: 623. Strain: 2457t. Gene: spal, mxib, spa47, cp0149. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.70Å     R-factor:   0.203     R-free:   0.259
Authors: Y.Morales,S.J.Johnson,J.L.Burgess,R.A.Burgess,N.E.Dickenson
Key ref: J.L.Burgess et al. (2016). Structural and Biochemical Characterization of Spa47 Provides Mechanistic Insight into Type III Secretion System ATPase Activation and Shigella Virulence Regulation. J Biol Chem, 291, 25837-25852. PubMed id: 27770024 DOI: 10.1074/jbc.M116.755256
Date:
08-Aug-16     Release date:   02-Nov-16    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
P0A1C1  (SPAL_SHIFL) -  Type 3 secretion system ATPase from Shigella flexneri
Seq:
Struc:
430 a.a.
336 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.7.4.2.8  - protein-secreting ATPase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: ATP + H2O + cellular proteinSide 1 = ADP + phosphate + cellular proteinSide 2
ATP
+ H2O
+ cellular proteinSide 1
= ADP
+ phosphate
+ cellular proteinSide 2
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
DOI no: 10.1074/jbc.M116.755256 J Biol Chem 291:25837-25852 (2016)
PubMed id: 27770024  
 
 
Structural and Biochemical Characterization of Spa47 Provides Mechanistic Insight into Type III Secretion System ATPase Activation and Shigella Virulence Regulation.
J.L.Burgess, R.A.Burgess, Y.Morales, J.M.Bouvang, S.J.Johnson, N.E.Dickenson.
 
  ABSTRACT  
 
No abstract given.

 

 

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