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PDBsum entry 3utt

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

 

 

 

 

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Contents
Protein chains
275 a.a.
100 a.a.
199 a.a.
244 a.a.
Ligands
ALA-LEU-TRP-GLY-
PRO-ASP-PRO-ALA-
ALA-ALA
×2
Waters ×151
PDB id:
3utt
Name: Immune system
Title: 1e6-a 0201-Alwgpdpaaa complex, triclinic
Structure: Hla class i histocompatibility antigen, a-2 alpha chain. Chain: a, f. Fragment: unp residues 25-299. Synonym: mhc class i heavy chain, mhc class i antigen a 2. Engineered: yes. Beta-2-microglobulin. Chain: b, g. Fragment: unp residues 21-119. Engineered: yes.
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: hla-a, hlaa. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: b2m, cdabp0092, hdcma22p. Synthetic: yes.
Resolution:
2.60Å     R-factor:   0.199     R-free:   0.274
Authors: P.J.Rizkallah,D.K.Cole,A.K.Sewell,A.M.Bulek,J.Rossjohn,S.Gras
Key ref: A.M.Bulek et al. (2012). Structural basis for the killing of human beta cells by CD8(+) T cells in type 1 diabetes. Nat Immunol, 13, 283-289. PubMed id: 22245737
Date:
26-Nov-11     Release date:   25-Jan-12    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P04439  (1A03_HUMAN) -  HLA class I histocompatibility antigen, A alpha chain from Homo sapiens
Seq:
Struc:
365 a.a.
275 a.a.*
Protein chains
Pfam   ArchSchema ?
P61769  (B2MG_HUMAN) -  Beta-2-microglobulin from Homo sapiens
Seq:
Struc:
119 a.a.
100 a.a.*
Protein chains
No UniProt id for this chain
Struc: 199 a.a.
Protein chains
No UniProt id for this chain
Struc: 244 a.a.
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 20 residue positions (black crosses)

 

 
Nat Immunol 13:283-289 (2012)
PubMed id: 22245737  
 
 
Structural basis for the killing of human beta cells by CD8(+) T cells in type 1 diabetes.
A.M.Bulek, D.K.Cole, A.Skowera, G.Dolton, S.Gras, F.Madura, A.Fuller, J.J.Miles, E.Gostick, D.A.Price, J.W.Drijfhout, R.R.Knight, G.C.Huang, N.Lissin, P.E.Molloy, L.Wooldridge, B.K.Jakobsen, J.Rossjohn, M.Peakman, P.J.Rizkallah, A.K.Sewell.
 
  ABSTRACT  
 
No abstract given.

 

 

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