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PDBsum entry 4p5e

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protein ligands metals Protein-protein interface(s) links
Hydrolase PDB id
4p5e

 

 

 

 

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Contents
Protein chains
140 a.a.
Ligands
N6P ×2
Metals
_CA
Waters ×387
PDB id:
4p5e
Name: Hydrolase
Title: Crystal structure of human dnph1 (rcl) with 6-naphthyl-purine- riboside-monophosphate
Structure: 2'-deoxynucleoside 5'-phosphate n-hydrolase 1. Chain: a, b. Synonym: c-myc-responsive protein rcl. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: dnph1, c6orf108, rcl. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
1.35Å     R-factor:   0.156     R-free:   0.180
Authors: A.Padilla,G.Labesse,P.A.Kaminski
Key ref: C.Amiable et al. (2014). 6-(Hetero)Arylpurine nucleotides as inhibitors of the oncogenic target DNPH1: synthesis, structural studies and cytotoxic activities. Eur J Med Chem, 85, 418-437. PubMed id: 25108359 DOI: 10.1016/j.ejmech.2014.07.110
Date:
16-Mar-14     Release date:   20-Aug-14    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
O43598  (DNPH1_HUMAN) -  2'-deoxynucleoside 5'-phosphate N-hydrolase 1 from Homo sapiens
Seq:
Struc:
174 a.a.
140 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 3 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: E.C.3.2.2.-  - ?????
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

 
DOI no: 10.1016/j.ejmech.2014.07.110 Eur J Med Chem 85:418-437 (2014)
PubMed id: 25108359  
 
 
6-(Hetero)Arylpurine nucleotides as inhibitors of the oncogenic target DNPH1: synthesis, structural studies and cytotoxic activities.
C.Amiable, J.Paoletti, A.Haouz, A.Padilla, G.Labesse, P.A.Kaminski, S.Pochet.
 
  ABSTRACT  
 
No abstract given.

 

 

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