spacer
spacer

PDBsum entry 3pmw

Go to PDB code: 
protein ligands links
Transport protein PDB id
3pmw

 

 

 

 

Loading ...

 
JSmol PyMol  
Contents
Protein chain
261 a.a. *
Ligands
GLU
SO4 ×7
GOL ×2
DMS
G69
Waters ×148
* Residue conservation analysis
PDB id:
3pmw
Name: Transport protein
Title: Ligand-binding domain of glua2 (flip) ionotropic glutamate receptor in complex with an allosteric modulator
Structure: Glutamate receptor 2. Chain: a. Fragment: ligand binding domain, residues 413 to 527 and 653 to 796. Synonym: glur-2, ampa-selective glutamate receptor 2, glur-b, glur- k2, glutamate receptor ionotropic, ampa 2, glua2. Engineered: yes. Mutation: yes. Other_details: s1-s2 fusion in which gly118 and thr119 replace a membrane-spanning region
Source: Rattus norvegicus. Brown rat,rat,rats. Organism_taxid: 10116. Gene: glur2, gria2. Expressed in: escherichia coli. Expression_system_taxid: 469008.
Resolution:
2.20Å     R-factor:   0.229     R-free:   0.313
Authors: J.K.F.Maclean,C.Jamieson,C.I.Brown,R.A.Campbell,K.J.Gillen, J.Gillespie,B.Kazemier,M.Kiczun,Y.Lamont,A.J.Lyons,E.M.Moir, J.A.Morrow,J.Pantling,Z.Rankovic,L.Smith
Key ref: C.Jamieson et al. (2011). Structure based evolution of a novel series of positive modulators of the AMPA receptor. Bioorg Med Chem Lett, 21, 805-811. PubMed id: 21190850
Date:
18-Nov-10     Release date:   12-Jan-11    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chain
Pfam   ArchSchema ?
P19491  (GRIA2_RAT) -  Glutamate receptor 2 from Rattus norvegicus
Seq:
Struc:
 
Seq:
Struc:
883 a.a.
261 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 7 residue positions (black crosses)

 

 
Bioorg Med Chem Lett 21:805-811 (2011)
PubMed id: 21190850  
 
 
Structure based evolution of a novel series of positive modulators of the AMPA receptor.
C.Jamieson, J.K.Maclean, C.I.Brown, R.A.Campbell, K.J.Gillen, J.Gillespie, B.Kazemier, M.Kiczun, Y.Lamont, A.J.Lyons, E.M.Moir, J.A.Morrow, J.Pantling, Z.Rankovic, L.Smith.
 
  ABSTRACT  
 
Starting from compound 1, we utilized biostructural data to successfully evolve an existing series into a new chemotype with a promising overall profile, exemplified by 19.
 

 

spacer

spacer