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PDBsum entry 5dnx

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protein ligands metals Protein-protein interface(s) links
Lyase PDB id
5dnx

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
176 a.a.
Ligands
5LD ×3
Metals
_MN ×6
Waters ×322
PDB id:
5dnx
Name: Lyase
Title: Crystal structure of igpd from pyrococcus furiosus in complex with (r)-c348
Structure: Imidazoleglycerol-phosphate dehydratase. Chain: a, c, b. Synonym: igpd. Engineered: yes
Source: Pyrococcus furiosus. Organism_taxid: 2261. Gene: hisb, pf1660. Expressed in: escherichia coli. Expression_system_taxid: 562
Resolution:
1.80Å     R-factor:   0.132     R-free:   0.158
Authors: C.Bisson,K.L.Britton,S.E.Sedelnikova,H.F.Rodgers,T.C.Eadsforth, R.C.Viner,T.R.Hawkes,P.J.Baker,D.W.Rice
Key ref: C.Bisson et al. (2016). Mirror-Image Packing Provides a Molecular Basis for the Nanomolar Equipotency of Enantiomers of an Experimental Herbicide. Angew Chem Int Ed Engl, 55, 13485-13489. PubMed id: 27717128 DOI: 10.1002/anie.201607185
Date:
10-Sep-15     Release date:   05-Oct-16    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P58880  (HIS7_PYRFU) -  Imidazoleglycerol-phosphate dehydratase from Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1)
Seq:
Struc:
176 a.a.
176 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 Enzyme reactions 
   Enzyme class: E.C.4.2.1.19  - imidazoleglycerol-phosphate dehydratase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

      Pathway:
Histidine Biosynthesis (late stages)
      Reaction: D-erythro-1-(imidazol-4-yl)glycerol 3-phosphate = 3-(imidazol-4-yl)-2- oxopropyl phosphate + H2O
D-erythro-1-(imidazol-4-yl)glycerol 3-phosphate
Bound ligand (Het Group name = 5LD)
matches with 40.00% similarity
= 3-(imidazol-4-yl)-2- oxopropyl phosphate
+ H2O
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
DOI no: 10.1002/anie.201607185 Angew Chem Int Ed Engl 55:13485-13489 (2016)
PubMed id: 27717128  
 
 
Mirror-Image Packing Provides a Molecular Basis for the Nanomolar Equipotency of Enantiomers of an Experimental Herbicide.
C.Bisson, K.L.Britton, S.E.Sedelnikova, H.F.Rodgers, T.C.Eadsforth, R.C.Viner, T.R.Hawkes, P.J.Baker, D.W.Rice.
 
  ABSTRACT  
 
No abstract given.

 

 

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