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PDBsum entry 2x5h

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protein ligands Protein-protein interface(s) links
Viral protein PDB id
2x5h

 

 

 

 

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Contents
Protein chains
92 a.a.
Ligands
SO4
Waters ×380
PDB id:
2x5h
Name: Viral protein
Title: Crystal structure of the orf131 l26m l51m double mutant from sulfolobus islandicus rudivirus 1
Structure: Orf 131. Chain: a, b, c, d. Fragment: truncated version, residues 1-96. Synonym: uncharacterized protein 131, cag38830. Engineered: yes. Mutation: yes
Source: Sulfolobus islandicus rudivirus 1. Organism_taxid: 282066. Variant: xx. Expressed in: escherichia coli. Expression_system_taxid: 511693. Expression_system_variant: bl21.
Resolution:
1.80Å     R-factor:   0.203     R-free:   0.257
Authors: M.Oke,L.G.Carter,K.A.Johnson,H.Liu,S.A.Mcmahon,J.H.Naismith,M.F.White
Key ref: M.Oke et al. (2010). The Scottish Structural Proteomics Facility: targets, methods and outputs. J Struct Funct Genomics, 11, 167-180. PubMed id: 20419351
Date:
08-Feb-10     Release date:   21-Jul-10    
PROCHECK
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 Headers
 References

Protein chains
Q8QL44  (Y131_SIRV1) -  Uncharacterized protein 131 from Sulfolobus islandicus rod-shaped virus 1
Seq:
Struc:
131 a.a.
92 a.a.*
Key:    Secondary structure  CATH domain
* PDB and UniProt seqs differ at 2 residue positions (black crosses)

 

 
J Struct Funct Genomics 11:167-180 (2010)
PubMed id: 20419351  
 
 
The Scottish Structural Proteomics Facility: targets, methods and outputs.
M.Oke, L.G.Carter, K.A.Johnson, H.Liu, S.A.McMahon, X.Yan, M.Kerou, N.D.Weikart, N.Kadi, M.A.Sheikh, S.Schmelz, M.Dorward, M.Zawadzki, C.Cozens, H.Falconer, H.Powers, I.M.Overton, C.A.van Niekerk, X.Peng, P.Patel, R.A.Garrett, D.Prangishvili, C.H.Botting, P.J.Coote, D.T.Dryden, G.J.Barton, U.Schwarz-Linek, G.L.Challis, G.L.Taylor, M.F.White, J.H.Naismith.
 
  ABSTRACT  
 
The Scottish Structural Proteomics Facility was funded to develop a laboratory scale approach to high throughput structure determination. The effort was successful in that over 40 structures were determined. These structures and the methods harnessed to obtain them are reported here. This report reflects on the value of automation but also on the continued requirement for a high degree of scientific and technical expertise. The efficiency of the process poses challenges to the current paradigm of structural analysis and publication. In the 5 year period we published ten peer-reviewed papers reporting structural data arising from the pipeline. Nevertheless, the number of structures solved exceeded our ability to analyse and publish each new finding. By reporting the experimental details and depositing the structures we hope to maximize the impact of the project by allowing others to follow up the relevant biology.
 

Literature references that cite this PDB file's key reference

  PubMed id Reference
22993091 G.Hagelueken, H.Huang, K.Harlos, B.R.Clarke, C.Whitfield, and J.H.Naismith (2012).
Crystallization, dehydration and experimental phasing of WbdD, a bifunctional kinase and methyltransferase from Escherichia coli O9a.
  Acta Crystallogr D Biol Crystallogr, 68, 1371-1379.
PDB code: 4ax8
21055949 H.J.Kang, and E.N.Baker (2011).
Intramolecular isopeptide bonds: protein crosslinks built for stress?
  Trends Biochem Sci, 36, 229-237.  
21342472 V.H.Tierrafría, H.E.Ramos-Aboites, G.Gosset, and F.Barona-Gómez (2011).
Disruption of the siderophore-binding desE receptor gene in Streptomyces coelicolor A3(2) results in impaired growth in spite of multiple iron-siderophore transport systems.
  Microb Biotechnol, 4, 275-285.  
21371926 Y.S.Choong, T.S.Lim, A.L.Chew, I.Aziah, and A.Ismail (2011).
Structural and functional studies of a 50 kDa antigenic protein from Salmonella enterica serovar Typhi.
  J Mol Graph Model, 29, 834-842.  
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 code is shown on the right.

 

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