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PDBsum entry 4kv5

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protein Protein-protein interface(s) links
Immune system PDB id
4kv5

 

 

 

 

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Contents
Protein chains
112 a.a.
230 a.a.
PDB id:
4kv5
Name: Immune system
Title: Scfv gc1009 in complex with tgf-beta1.
Structure: Transforming growth factor beta-1 proprotein. Chain: c, d, a, b. Fragment: unp residues 279-390. Engineered: yes. Single-chain variable fragment gc1009. Chain: j, h, e, g. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: tgfb1, tgfb. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
3.00Å     R-factor:   0.233     R-free:   0.300
Authors: R.Wei,A.G.Moulin,M.Mathieu
Key ref: A.Moulin et al. (2014). Structures of a pan-specific antagonist antibody complexed to different isoforms of TGFβ reveal structural plasticity of antibody-antigen interactions. Protein Sci, 23, 1698-1707. PubMed id: 25209176 DOI: 10.1002/pro.2548
Date:
22-May-13     Release date:   24-Sep-14    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P01137  (TGFB1_HUMAN) -  Transforming growth factor beta-1 proprotein from Homo sapiens
Seq:
Struc:
390 a.a.
112 a.a.
Protein chains
No UniProt id for this chain
Struc: 230 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
DOI no: 10.1002/pro.2548 Protein Sci 23:1698-1707 (2014)
PubMed id: 25209176  
 
 
Structures of a pan-specific antagonist antibody complexed to different isoforms of TGFβ reveal structural plasticity of antibody-antigen interactions.
A.Moulin, M.Mathieu, C.Lawrence, R.Bigelow, M.Levine, C.Hamel, J.P.Marquette, J.Le Parc, C.Loux, P.Ferrari, C.Capdevila, J.Dumas, B.Dumas, A.Rak, J.Bird, H.Qiu, C.Q.Pan, T.Edmunds, R.R.Wei.
 
  ABSTRACT  
 
Various important biological pathways are modulated by TGFβ isoforms; as such they are potential targets for therapeutic intervention. Fresolimumab, also known as GC1008, is a pan-TGFβ neutralizing antibody that has been tested clinically for several indications including an ongoing trial for focal segmental glomerulosclerosis. The structure of the antigen-binding fragment of fresolimumab (GC1008 Fab) in complex with TGFβ3 has been reported previously, but the structural capacity of fresolimumab to accommodate tight interactions with TGFβ1 and TGFβ2 was insufficiently understood. We report the crystal structure of the single-chain variable fragment of fresolimumab (GC1008 scFv) in complex with target TGFβ1 to a resolution of 3.00 Å and the crystal structure of GC1008 Fab in complex with TGFβ2 to 2.83 Å. The structures provide further insight into the details of TGFβ recognition by fresolimumab, give a clear indication of the determinants of fresolimumab pan-specificity and provide potential starting points for the development of isoform-specific antibodies using a fresolimumab scaffold.
 

 

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