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PDBsum entry 5dc9

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protein ligands Protein-protein interface(s) links
Protein binding PDB id
5dc9

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
100 a.a.
94 a.a.
Ligands
GOL ×5
IMD ×2
Waters ×232
PDB id:
5dc9
Name: Protein binding
Title: Crystal structure of monobody as25/abl1 sh2 domain complex, crystal b
Structure: Tyrosine-protein kinase abl1. Chain: a. Synonym: abelson murine leukemia viral oncogene homolog 1,abelson tyrosine-protein kinase 1,proto-oncogenE C-abl,p150. Engineered: yes. As25 monobody. Chain: b. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: abl1, abl, jtk7. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
1.56Å     R-factor:   0.138     R-free:   0.171
Authors: J.B.Wojcik,A.Koide,S.Koide
Key ref: J.Wojcik et al. (2016). Allosteric Inhibition of Bcr-Abl Kinase by High Affinity Monobody Inhibitors Directed to the Src Homology 2 (SH2)-Kinase Interface. J Biol Chem, 291, 8836-8847. PubMed id: 26912659 DOI: 10.1074/jbc.M115.707901
Date:
23-Aug-15     Release date:   02-Mar-16    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P00519  (ABL1_HUMAN) -  Tyrosine-protein kinase ABL1 from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1130 a.a.
100 a.a.
Protein chain
Pfam   ArchSchema ?
P02751  (FINC_HUMAN) -  Fibronectin from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
2477 a.a.
94 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 20 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: Chain A: E.C.2.7.10.2  - non-specific protein-tyrosine kinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H+
L-tyrosyl-[protein]
+ ATP
= O-phospho-L-tyrosyl-[protein]
+ ADP
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
DOI no: 10.1074/jbc.M115.707901 J Biol Chem 291:8836-8847 (2016)
PubMed id: 26912659  
 
 
Allosteric Inhibition of Bcr-Abl Kinase by High Affinity Monobody Inhibitors Directed to the Src Homology 2 (SH2)-Kinase Interface.
J.Wojcik, A.J.Lamontanara, G.Grabe, A.Koide, L.Akin, B.Gerig, O.Hantschel, S.Koide.
 
  ABSTRACT  
 
No abstract given.

 

 

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