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PDBsum entry 4tq7

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protein Protein-protein interface(s) links
Structural protein PDB id
4tq7

 

 

 

 

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Contents
Protein chains
140 a.a.
Waters ×84
PDB id:
4tq7
Name: Structural protein
Title: N-terminal domain of c. Reinhardtii sas-6 homolog bld12p q93e (nn10)
Structure: Centriole protein. Chain: a, b. Synonym: n-terminal domain of c. Reinhardtii sas-6 homolog bld12p q93e (nn10). Engineered: yes. Mutation: yes
Source: Chlamydomonas reinhardtii. Organism_taxid: 3055. Gene: crsas-6. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008
Resolution:
2.64Å     R-factor:   0.210     R-free:   0.258
Authors: M.Hilbert,S.H.W.Kraatz
Key ref: M.Hilbert et al. (2016). SAS-6 engineering reveals interdependence between cartwheel and microtubules in determining centriole architecture. Nat Cell Biol, 18, 393-403. PubMed id: 26999736 DOI: 10.1038/ncb3329
Date:
10-Jun-14     Release date:   24-Jun-15    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
A9CQL4  (A9CQL4_CHLRE) -  Centriole protein from Chlamydomonas reinhardtii
Seq:
Struc:
 
Seq:
Struc:
728 a.a.
140 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 1 residue position (black cross)

 

 
DOI no: 10.1038/ncb3329 Nat Cell Biol 18:393-403 (2016)
PubMed id: 26999736  
 
 
SAS-6 engineering reveals interdependence between cartwheel and microtubules in determining centriole architecture.
M.Hilbert, A.Noga, D.Frey, V.Hamel, P.Guichard, S.H.Kraatz, M.Pfreundschuh, S.Hosner, I.Flückiger, R.Jaussi, M.M.Wieser, K.M.Thieltges, X.Deupi, D.J.Müller, R.A.Kammerer, P.Gönczy, M.Hirono, M.O.Steinmetz.
 
  ABSTRACT  
 
Centrioles are critical for the formation of centrosomes, cilia and flagella in eukaryotes. They are thought to assemble around a nine-fold symmetric cartwheel structure established by SAS-6 proteins. Here, we have engineered Chlamydomonas reinhardtii SAS-6-based oligomers with symmetries ranging from five- to ten-fold. Expression of a SAS-6 mutant that forms six-fold symmetric cartwheel structures in vitro resulted in cartwheels and centrioles with eight- or nine-fold symmetries in vivo. In combination with Bld10 mutants that weaken cartwheel-microtubule interactions, this SAS-6 mutant produced six- to eight-fold symmetric cartwheels. Concurrently, the microtubule wall maintained eight- and nine-fold symmetries. Expressing SAS-6 with analogous mutations in human cells resulted in nine-fold symmetric centrioles that exhibited impaired length and organization. Together, our data suggest that the self-assembly properties of SAS-6 instruct cartwheel symmetry, and lead us to propose a model in which the cartwheel and the microtubule wall assemble in an interdependent manner to establish the native architecture of centrioles.
 

 

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