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PDBsum entry 2b60

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protein ligands Protein-protein interface(s) links
Hydrolase/hydrolase inhibitor PDB id
2b60

 

 

 

 

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Contents
Protein chains
99 a.a. *
Ligands
GOL
RIT
Waters ×75
* Residue conservation analysis
PDB id:
2b60
Name: Hydrolase/hydrolase inhibitor
Title: Structure of HIV-1 protease mutant bound to ritonavir
Structure: Gag-pol polyprotein. Chain: a, b. Fragment: protease. Engineered: yes. Mutation: yes
Source: Human immunodeficiency virus 1. Organism_taxid: 11676. Expressed in: escherichia coli. Expression_system_taxid: 562.
Biol. unit: Dimer (from PQS)
Resolution:
2.20Å     R-factor:   0.216     R-free:   0.245
Authors: J.C.Clemente,L.R.Stow,L.K.Janka,J.A.Jeung,K.A.Desai,L.Govindasamy, M.Agbandje-Mckenna,R.Mckenna,M.M.Goodenow,B.M.Dunn
Key ref: J.C.Clemente et al. In vivo, Kinetic, And structural analysis of the development of ritonavir resistance. To be published, .
Date:
29-Sep-05     Release date:   14-Nov-06    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
Q7SMT3  (Q7SMT3_9HIV1) -  Pol polyprotein (Fragment) from Human immunodeficiency virus 1
Seq:
Struc:
358 a.a.
99 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 4 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: E.C.?
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

 

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