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PDBsum entry 3scm

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protein ligands Protein-protein interface(s) links
Immune system PDB id
3scm

 

 

 

 

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Contents
Protein chains
289 a.a.
99 a.a.
191 a.a.
239 a.a.
Ligands
NAG-NAG
NAG ×2
LGN
Waters ×129
PDB id:
3scm
Name: Immune system
Title: Crystal structure of autoreactive-valpha14-vbeta6 nkt tcr in complex with cd1d-isoglobotrihexosylceramide
Structure: Antigen-presenting glycoprotein cd1d1. Chain: a. Fragment: extracellular domain, unp residues 19-297. Engineered: yes. Beta-2-microglobulin. Chain: b. Fragment: extracellular domain, unp residues 21-119. Engineered: yes. Nkt tcr valpha14 chain.
Source: Mus musculus. Mouse. Organism_taxid: 10090. Gene: cd1d1, cd1.1. Expressed in: trichoplusia ni. Expression_system_taxid: 7111. Expression_system_cell_line: hi5. Gene: b2m. Mus musculus , homo sapiens.
Resolution:
2.50Å     R-factor:   0.275     R-free:   0.318
Authors: A.J.Clarke,J.Rossjohn
Key ref: D.G.Pellicci et al. (2011). Recognition of β-linked self glycolipids mediated by natural killer T cell antigen receptors. Nat Immunol, 12, 827-833. PubMed id: 21804559
Date:
08-Jun-11     Release date:   05-Oct-11    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P11609  (CD1D1_MOUSE) -  Antigen-presenting glycoprotein CD1d1 from Mus musculus
Seq:
Struc:
336 a.a.
289 a.a.*
Protein chain
Pfam   ArchSchema ?
P01887  (B2MG_MOUSE) -  Beta-2-microglobulin from Mus musculus
Seq:
Struc:
119 a.a.
99 a.a.
Protein chain
Pfam   ArchSchema ?
P01848  (TCA_HUMAN) -  T cell receptor alpha chain constant from Homo sapiens
Seq:
Struc:
140 a.a.
191 a.a.*
Protein chain
No UniProt id for this chain
Struc: 239 a.a.
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 18 residue positions (black crosses)

 

 
Nat Immunol 12:827-833 (2011)
PubMed id: 21804559  
 
 
Recognition of β-linked self glycolipids mediated by natural killer T cell antigen receptors.
D.G.Pellicci, A.J.Clarke, O.Patel, T.Mallevaey, T.Beddoe, J.Le Nours, A.P.Uldrich, J.McCluskey, G.S.Besra, S.A.Porcelli, L.Gapin, D.I.Godfrey, J.Rossjohn.
 
  ABSTRACT  
 
No abstract given.

 

 

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