spacer
spacer

PDBsum entry 2x9c

Go to PDB code: 
protein Protein-protein interface(s) links
Protein transport PDB id
2x9c

 

 

 

 

Loading ...

 
JSmol PyMol  
Contents
Protein chains
62 a.a. *
Waters ×9
* Residue conservation analysis
PDB id:
2x9c
Name: Protein transport
Title: Crystal structure of a soluble prgi mutant from salmonella typhimurium
Structure: Protein prgi. Chain: a, b. Synonym: prgi. Engineered: yes. Mutation: yes
Source: Salmonella typhimurium. Organism_taxid: 216597. Strain: sl1344. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
2.45Å     R-factor:   0.225     R-free:   0.239
Authors: O.Poyraz,H.Schmidt,K.Seidel,F.Delissen,C.Ader,H.Tenenboim,C.Goosmann, B.Laube,A.F.Thuenemann,A.Zychlinsky,M.Baldus,A.Lange,C.Griesinger, M.Kolbe
Key ref: O.Poyraz et al. (2010). Protein refolding is required for assembly of the type three secretion needle. Nat Struct Biol, 17, 788-792. PubMed id: 20543831
Date:
15-Mar-10     Release date:   16-Jun-10    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
P41784  (PRGI_SALTY) -  SPI-1 type 3 secretion system needle filament protein from Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720)
Seq:
Struc:
80 a.a.
62 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 2 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: E.C.?
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
Nat Struct Biol 17:788-792 (2010)
PubMed id: 20543831  
 
 
Protein refolding is required for assembly of the type three secretion needle.
O.Poyraz, H.Schmidt, K.Seidel, F.Delissen, C.Ader, H.Tenenboim, C.Goosmann, B.Laube, A.F.Thünemann, A.Zychlinsky, M.Baldus, A.Lange, C.Griesinger, M.Kolbe.
 
  ABSTRACT  
 
Pathogenic Gram-negative bacteria use a type three secretion system (TTSS) to deliver virulence factors into host cells. Although the order in which proteins incorporate into the growing TTSS is well described, the underlying assembly mechanisms are still unclear. Here we show that the TTSS needle protomer refolds spontaneously to extend the needle from the distal end. We developed a functional mutant of the needle protomer from Shigella flexneri and Salmonella typhimurium to study its assembly in vitro. We show that the protomer partially refolds from alpha-helix into beta-strand conformation to form the TTSS needle. Reconstitution experiments show that needle growth does not require ATP. Thus, like the structurally related flagellar systems, the needle elongates by subunit polymerization at the distal end but requires protomer refolding. Our studies provide a starting point to understand the molecular assembly mechanisms and the structure of the TTSS at atomic level.
 

Literature references that cite this PDB file's key reference

  PubMed id Reference
21112241 L.J.Worrall, E.Lameignere, and N.C.Strynadka (2011).
Structural overview of the bacterial injectisome.
  Curr Opin Microbiol, 14, 3-8.  
21031487 S.Chatterjee, D.Zhong, B.A.Nordhues, K.P.Battaile, S.Lovell, and R.N.De Guzman (2011).
The crystal structures of the Salmonella type III secretion system tip protein SipD in complex with deoxycholate and chenodeoxycholate.
  Protein Sci, 20, 75-86.
PDB codes: 3nzz 3o00 3o01 3o02
The most recent references are shown first. Citation data come partly from CiteXplore and partly from an automated harvesting procedure. Note that this is likely to be only a partial list as not all journals are covered by either method. However, we are continually building up the citation data so more and more references will be included with time. Where a reference describes a PDB structure, the PDB codes are shown on the right.

 

spacer

spacer