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PDBsum entry 2xae

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protein ligands metals Protein-protein interface(s) links
Cell cycle PDB id
2xae

 

 

 

 

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Contents
Protein chains
328 a.a.
Ligands
2XA ×3
ADP ×3
SO4 ×3
Metals
_CL
_MG ×3
Waters ×366
PDB id:
2xae
Name: Cell cycle
Title: Crystal structure of human kinesin eg5 in complex with (r)-2-amino-3- ((s)-2-methyl-1,1-diphenylbutylthio)propanoic acid
Structure: Kinesin-like protein kif11. Chain: a, b, c. Fragment: motor domain, residues 1-368. Synonym: eg5, kinesin-related motor protein eg5, kinesin-like spindle protein hksp, thyroid receptor-interacting protein 5, tr-interacting protein 5, trip-5, kinesin-like protein 1. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Expressed in: escherichia coli. Expression_system_taxid: 469008. Expression_system_variant: plyss
Resolution:
2.60Å     R-factor:   0.185     R-free:   0.257
Authors: H.Y.K.Kaan,J.Weiss,D.Menger,V.Ulaganathan,K.Tkocz,C.Laggner, F.Popowycz,B.Joseph,F.Kozielski
Key ref: H.Y.Kaan et al. (2011). Structure-activity relationship and multidrug resistance study of new S-trityl-L-cysteine derivatives as inhibitors of Eg5. J Med Chem, 54, 1576-1586. PubMed id: 21344920
Date:
31-Mar-10     Release date:   30-Mar-11    
PROCHECK
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 Headers
 References

Protein chains
Pfam   ArchSchema ?
P52732  (KIF11_HUMAN) -  Kinesin-like protein KIF11 from Homo sapiens
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1056 a.a.
328 a.a.
Key:    PfamA domain  Secondary structure  CATH domain

 

 
J Med Chem 54:1576-1586 (2011)
PubMed id: 21344920  
 
 
Structure-activity relationship and multidrug resistance study of new S-trityl-L-cysteine derivatives as inhibitors of Eg5.
H.Y.Kaan, J.Weiss, D.Menger, V.Ulaganathan, K.Tkocz, C.Laggner, F.Popowycz, B.Joseph, F.Kozielski.
 
  ABSTRACT  
 
No abstract given.

 

 

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