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PDBsum entry 3d9c

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protein ligands links
Hydrolase PDB id
3d9c

 

 

 

 

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Contents
Protein chain
282 a.a. *
Ligands
ZYZ
Waters ×47
* Residue conservation analysis
PDB id:
3d9c
Name: Hydrolase
Title: Crystal structure ptp1b complex with aryl seleninic acid
Structure: Tyrosine-protein phosphatase non-receptor type 1. Chain: a. Fragment: unp residues 1-283. Synonym: protein-tyrosine phosphatase 1b, ptp-1b. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: ptpn1, ptp1b. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.30Å     R-factor:   0.218     R-free:   0.274
Authors: M.Abdo,S.Liu,B.Zhou,C.D.Walls,S.Knapp,Z.-Y.Zhang
Key ref: M.Abdo et al. (2008). Seleninate in place of phosphate: irreversible inhibition of protein tyrosine phosphatases. J Am Chem Soc, 130, 13196-13197. PubMed id: 18781746
Date:
27-May-08     Release date:   23-Sep-08    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P18031  (PTN1_HUMAN) -  Tyrosine-protein phosphatase non-receptor type 1 from Homo sapiens
Seq:
Struc:
435 a.a.
282 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.3.1.3.48  - protein-tyrosine-phosphatase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: O-phospho-L-tyrosyl-[protein] + H2O = L-tyrosyl-[protein] + phosphate
O-phospho-L-tyrosyl-[protein]
+ H2O
= L-tyrosyl-[protein]
+ phosphate
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Key reference    
 
 
J Am Chem Soc 130:13196-13197 (2008)
PubMed id: 18781746  
 
 
Seleninate in place of phosphate: irreversible inhibition of protein tyrosine phosphatases.
M.Abdo, S.Liu, B.Zhou, C.D.Walls, L.Wu, S.Knapp, Z.Y.Zhang.
 
  ABSTRACT  
 
A homotyrosine based seleninic acid irreversibly inhibits protein tyrosine phosphatases by forming a covalent selenosulfide linkage with the active site cysteine sulfhydryl specifically. The details of the event are revealed by model synthetic studies and by kinetic, mass spectrometric, and crystallographic characterization.
 

 

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