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IID90032
UniprotP04586
ProteinGag-Pol polyprotein
Genegag-pol
OrganismHuman immunodeficiency virus type 1 group M subtype D
Sequence LLPS PhaSepDB
PhaSePro
LLPSDB
DrLLPS
xml
Structure
Experiment
  :order   disorder   conflict   PDB cluster   ProS   Pfam Domain   SEG
148
 order/disorder by at least rule
     disorder by at least rule
     order by at least rule
 order/disorder by majority rule
Seq 80-130 Homo dimer :
 Evidence NMR 1ihw B Reference
       Region 1ihw B 80-130 order
 Evidence NMR 1ihw A Reference
       Region 1ihw A 80-130 order
 Evidence NMR 1ihv B Reference
       Region 1ihv B 80-130 order
 Evidence NMR 1ihv A Reference
       Region 1ihv A 80-130 order
 
Prediction
NeProc
Disorder 1-4,132-148
Order 5-73,81-131
ProS 1-4
AlphaFold
Disorder 131-148
Order 1-130
Pfam Hmmer
PF00552 80-130 9.4e-24
Function
Function in SwissProt
Integrase:Catalyzes viral DNA integration into the host chromosome, by performing a series of DNA cutting and joining reactions. This enzyme activity takes place after virion entry into a cell and reverse transcription of the RNA genome in dsDNA. The first step in the integration process is 3' processing. This step requires a complex comprising the viral genome, matrix protein, Vpr and integrase. This complex is called the pre-integration complex (PIC). The integrase protein removes 2 nucleotides from each 3' end of the viral DNA, leaving recessed CA OH's at the 3' ends. In the second step, the PIC enters cell nucleus. This process is mediated through integrase and Vpr proteins, and allows the virus to infect a non dividing cell. This ability to enter the nucleus is specific of lentiviruses, other retroviruses cannot and rely on cell division to access cell chromosomes. In the third step, termed strand transfer, the integrase protein joins the previously processed 3' ends to the 5' ends of strands of target cellular DNA at the site of integration. The 5'-ends are produced by integrase-catalyzed staggered cuts, 5 bp apart. A Y-shaped, gapped, recombination intermediate results, with the 5'-ends of the viral DNA strands and the 3' ends of target DNA strands remaining unjoined, flanking a gap of 5 bp. The last step is viral DNA integration into host chromosome. This involves host DNA repair synthesis in which the 5 bp gaps between the unjoined strands are filled in and then ligated. Since this process occurs at both cuts flanking the HIV genome, a 5 bp duplication of host DNA is produced at the ends of HIV-1 integration. Alternatively, Integrase may catalyze the excision of viral DNA just after strand transfer, this is termed disintegration.