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PDBsum entry 4fww

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protein ligands links
Transferase PDB id
4fww

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
513 a.a.
Ligands
NAG-NAG-BMA-BMA
SO4 ×2
ACT ×5
GOL ×4
EDO ×4
PEG
Waters ×358
PDB id:
4fww
Name: Transferase
Title: Crystal structure of the sema-psi extracellular domains of human ron receptor tyrosine kinase
Structure: Macrophage-stimulating protein receptor. Chain: a. Fragment: extracellular sema and psi domains (unp residues 42-568). Synonym: msp receptor, cdw136, protein-tyrosine kinase 8, p185-ron, macrophage-stimulating protein receptor alpha chain, macrophage- stimulating protein receptor beta chain. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: mst1r, ptk8, ron. Expressed in: drosophila melanogaster. Expression_system_taxid: 7227.
Resolution:
1.85Å     R-factor:   0.193     R-free:   0.232
Authors: K.L.Chao,O.Herzberg
Key ref: K.L.Chao et al. (2012). Crystal structure of the Sema-PSI extracellular domain of human RON receptor tyrosine kinase. Plos One, 7, e41912. PubMed id: 22848655
Date:
02-Jul-12     Release date:   08-Aug-12    
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.
513 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 = NAG)
matches with 41.38% similarity
+ ADP
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
Plos One 7:e41912 (2012)
PubMed id: 22848655  
 
 
Crystal structure of the Sema-PSI extracellular domain of human RON receptor tyrosine kinase.
K.L.Chao, I.W.Tsai, C.Chen, O.Herzberg.
 
  ABSTRACT  
 
No abstract given.

 

 

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