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PDBsum entry 5ml2

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protein ligands links
Lipid binding protein PDB id
5ml2

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
144 a.a.
Ligands
NH6
Waters ×131
PDB id:
5ml2
Name: Lipid binding protein
Title: The crystal structure of pde6d in complex with inhibitor-3
Structure: Retinal rod rhodopsin-sensitive cgmp 3',5'-cyclic phosphodiesterase subunit delta. Chain: b. Synonym: gmp-pde delta,protein p17. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: pde6d, pded. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
1.60Å     R-factor:   0.204     R-free:   0.227
Authors: E.K.Fansa,P.Martin-Gago,H.Waldmann,A.Wittinghofer
Key ref: P.Martín-Gago et al. (2017). A PDE6δ-KRas Inhibitor Chemotype with up to Seven H-Bonds and Picomolar Affinity that Prevents Efficient Inhibitor Release by Arl2. Angew Chem Int Ed Engl, 56, 2423-2428. PubMed id: 28106325 DOI: 10.1002/anie.201610957
Date:
06-Dec-16     Release date:   01-Feb-17    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
O43924  (PDE6D_HUMAN) -  Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta from Homo sapiens
Seq:
Struc:
150 a.a.
144 a.a.
Key:    PfamA domain  Secondary structure

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

 

 
DOI no: 10.1002/anie.201610957 Angew Chem Int Ed Engl 56:2423-2428 (2017)
PubMed id: 28106325  
 
 
A PDE6δ-KRas Inhibitor Chemotype with up to Seven H-Bonds and Picomolar Affinity that Prevents Efficient Inhibitor Release by Arl2.
P.Martín-Gago, E.K.Fansa, C.H.Klein, S.Murarka, P.Janning, M.Schürmann, M.Metz, S.Ismail, C.Schultz-Fademrecht, M.Baumann, P.I.Bastiaens, A.Wittinghofer, H.Waldmann.
 
  ABSTRACT  
 
No abstract given.

 

 

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