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PDBsum entry 3pls

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protein ligands metals links
Transferase PDB id
3pls

 

 

 

 

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Contents
Protein chain
298 a.a. *
Ligands
ANP
Metals
_MG
Waters ×50
* Residue conservation analysis
PDB id:
3pls
Name: Transferase
Title: Ron in complex with ligand amp-pnp
Structure: Macrophage-stimulating protein receptor. Chain: a. Fragment: ron kinase domain residues 1060-1357. Synonym: msp receptor, cdw136, protein-tyrosine kinase 8, p185-ron, macrophage-stimulating protein receptor beta chain. Engineered: yes. Mutation: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: mst1r, ptk8, ron. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108.
Resolution:
2.24Å     R-factor:   0.235     R-free:   0.290
Authors: J.Wang,S.Steinbacher,M.Augustin,P.Schreiner,D.Epstein,M.J.Mulvihill, A.P.Crew
Key ref: J.Wang et al. (2010). The crystal structure of a constitutively active mutant RON kinase suggests an intramolecular autophosphorylation hypothesis. Biochemistry, 49, 7972-7974. PubMed id: 20726546
Date:
15-Nov-10     Release date:   24-Nov-10    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
Q04912  (RON_HUMAN) -  Macrophage-stimulating protein receptor from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1400 a.a.
298 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.2.7.10.1  - receptor 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]
Bound ligand (Het Group name = ANP)
matches with 81.25% similarity
+ ADP
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
Biochemistry 49:7972-7974 (2010)
PubMed id: 20726546  
 
 
The crystal structure of a constitutively active mutant RON kinase suggests an intramolecular autophosphorylation hypothesis.
J.Wang, S.Steinbacher, M.Augustin, P.Schreiner, D.Epstein, M.J.Mulvihill, A.P.Crew.
 
  ABSTRACT  
 
No abstract given.

 

 

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