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PDBsum entry 3am4

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protein ligands Protein-protein interface(s) links
Oxidoreductase/oxidoreductase inhibitor PDB id
3am4

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
287 a.a.
Ligands
NAD ×2
FT1 ×2
Waters ×212
PDB id:
3am4
Name: Oxidoreductase/oxidoreductase inhibitor
Title: A372m mutant of enoyl-acp reductase from plasmodium falciparum (pfenr) in complex with triclosan variant t1
Structure: Enoyl-acp reductase. Chain: a, b. Fragment: residues 96-424. Synonym: pfenr. Engineered: yes. Mutation: yes
Source: Plasmodium falciparum. Organism_taxid: 5833. Gene: fabi. Expressed in: escherichia coli. Expression_system_taxid: 562.
Resolution:
2.30Å     R-factor:   0.211     R-free:   0.261
Authors: K.Maity,T.Banerjee,P.Narayanappa,N.Surolia,A.Surolia,K.Suguna
Key ref: K.Maity et al. (2011). Effect of substrate binding loop mutations on the structure, kinetics, and inhibition of enoyl acyl carrier protein reductase from Plasmodium falciparum. Iubmb Life, 63, 30-41. PubMed id: 21280175
Date:
14-Aug-10     Release date:   16-Mar-11    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q9BJJ9  (Q9BJJ9_PLAFA) -  Enoyl-ACP reductase (Fragment) from Plasmodium falciparum
Seq:
Struc:
432 a.a.
287 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.1.3.1.9  - enoyl-[acyl-carrier-protein] reductase (NADH).
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: a 2,3-saturated acyl-[ACP] + NAD+ = a (2E)-enoyl-[ACP] + NADH + H+
2,3-saturated acyl-[ACP]
+
NAD(+)
Bound ligand (Het Group name = NAD)
corresponds exactly
= (2E)-enoyl-[ACP]
+ NADH
+ H(+)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
Iubmb Life 63:30-41 (2011)
PubMed id: 21280175  
 
 
Effect of substrate binding loop mutations on the structure, kinetics, and inhibition of enoyl acyl carrier protein reductase from Plasmodium falciparum.
K.Maity, T.Banerjee, N.Prabakaran, N.Surolia, A.Surolia, K.Suguna.
 
  ABSTRACT  
 
No abstract given.

 

 

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