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PDBsum entry 4rv3

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protein ligands links
Lyase PDB id
4rv3

 

 

 

 

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JSmol PyMol  
Contents
Protein chain
302 a.a.
Ligands
ACT
INS
Waters ×161
PDB id:
4rv3
Name: Lyase
Title: Crystal structure of a pentafluoro-phe incorporated phosphatidylinositol-specific phospholipasE C (h258x)from staphylococcus aureus
Structure: 1-phosphatidylinositol phosphodiesterase. Chain: a. Engineered: yes. Mutation: yes
Source: Staphylococcus aureus. Organism_taxid: 426430. Strain: newman. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
2.00Å     R-factor:   0.183     R-free:   0.238
Authors: T.He,A.Gershenson,S.J.Eyles,J.Gao,M.F.Roberts
Key ref: T.He et al. (2015). Fluorinated Aromatic Amino Acids Distinguish Cation-π Interactions from Membrane Insertion. J Biol Chem, 290, 19334-19342. PubMed id: 26092728 DOI: 10.1074/jbc.M115.668343
Date:
24-Nov-14     Release date:   01-Jul-15    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P45723  (PLC_STAAE) -  1-phosphatidylinositol phosphodiesterase from Staphylococcus aureus (strain Newman)
Seq:
Struc:
312 a.a.
302 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.4.6.1.13  - phosphatidylinositol diacylglycerol-lyase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

      Pathway:
1-Phosphatidyl-myo-inositol Metabolism
      Reaction: a 1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol) = 1D-myo-inositol 1,2-cyclic phosphate + a 1,2-diacyl-sn-glycerol
1,2-diacyl-sn-glycero-3-phospho-(1D-myo-inositol)
=
1D-myo-inositol 1,2-cyclic phosphate
Bound ligand (Het Group name = INS)
matches with 80.00% similarity
+ 1,2-diacyl-sn-glycerol
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
DOI no: 10.1074/jbc.M115.668343 J Biol Chem 290:19334-19342 (2015)
PubMed id: 26092728  
 
 
Fluorinated Aromatic Amino Acids Distinguish Cation-π Interactions from Membrane Insertion.
T.He, A.Gershenson, S.J.Eyles, Y.J.Lee, W.R.Liu, J.Wang, J.Gao, M.F.Roberts.
 
  ABSTRACT  
 
No abstract given.

 

 

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