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PDBsum entry 4obj

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protein ligands Protein-protein interface(s) links
Hydrolase PDB id
4obj

 

 

 

 

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JSmol PyMol  
Contents
Protein chains
99 a.a.
Ligands
ARG-PRO-GLY-ASN-
PHE-LEU-GLN-ASN-
ARG-PRO
GOL ×3
ACT ×3
EDO ×6
Waters ×160
PDB id:
4obj
Name: Hydrolase
Title: Crystal structure of inactive HIV-1 protease in complex with the p1-p6 substrate variant (s451n)
Structure: HIV-1 protease. Chain: a, b. Synonym: pr, retropepsin. Engineered: yes. Mutation: yes. P1-p6 peptide. Chain: c. Fragment: unp residues 446-455. Engineered: yes.
Source: Human immunodeficiency virus type 1. HIV-1. Organism_taxid: 11685. Strain: group m subtype b (isolate arv2/sf2). Gene: gag-pol. Expressed in: escherichia coli. Expression_system_taxid: 562. Synthetic: yes. Human immunodeficiency virus 1.
Resolution:
1.75Å     R-factor:   0.145     R-free:   0.183
Authors: M.Kolli
Key ref: M.Kolli et al. (2014). HIV-1 protease-substrate coevolution in nelfinavir resistance. J Virol, 88, 7145-7154. PubMed id: 24719428 DOI: 10.1128/JVI.00266-14
Date:
07-Jan-14     Release date:   26-Nov-14    
PROCHECK
Go to PROCHECK summary
 Headers
 References

Protein chains
Pfam   ArchSchema ?
P03369  (POL_HV1A2) -  Gag-Pol polyprotein from Human immunodeficiency virus type 1 group M subtype B (isolate ARV2/SF2)
Seq:
Struc:
 
Seq:
Struc:
 
Seq:
Struc:
1437 a.a.
99 a.a.*
Key:    PfamA domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 3 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class 1: E.C.2.7.7.-  - ?????
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
   Enzyme class 2: E.C.2.7.7.49  - RNA-directed Dna polymerase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: DNA(n) + a 2'-deoxyribonucleoside 5'-triphosphate = DNA(n+1) + diphosphate
DNA(n)
+ 2'-deoxyribonucleoside 5'-triphosphate
= DNA(n+1)
+ diphosphate
   Enzyme class 3: E.C.2.7.7.7  - DNA-directed Dna polymerase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: DNA(n) + a 2'-deoxyribonucleoside 5'-triphosphate = DNA(n+1) + diphosphate
DNA(n)
+ 2'-deoxyribonucleoside 5'-triphosphate
= DNA(n+1)
+ diphosphate
   Enzyme class 4: E.C.3.1.-.-
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
   Enzyme class 5: E.C.3.1.13.2  - exoribonuclease H.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Exonucleolytic cleavage to 5'-phosphomonoester oligonucleotides in both 5'- to 3'- and 3'- to 5'-directions.
   Enzyme class 6: E.C.3.1.26.13  - retroviral ribonuclease H.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
   Enzyme class 7: E.C.3.4.23.16  - HIV-1 retropepsin.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: Specific for a P1 residue that is hydrophobic, and P1' variable, but often Pro.
Note, where more than one E.C. class is given (as above), each may correspond to a different protein domain or, in the case of polyprotein precursors, to a different mature protein.
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
DOI no: 10.1128/JVI.00266-14 J Virol 88:7145-7154 (2014)
PubMed id: 24719428  
 
 
HIV-1 protease-substrate coevolution in nelfinavir resistance.
M.Kolli, A.Ozen, N.Kurt-Yilmaz, C.A.Schiffer.
 
  ABSTRACT  
 
No abstract given.

 

 

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