Detail Information for IndEnz0002011226
IED ID IndEnz0002011226
Enzyme Type ID protease011226
Protein Name Gag-Pol polyprotein
Pr160Gag-Pol

Cleaved into: Integrase
IN
EC 2.7.7.-
EC 3.1.-.-

Fragment
Gene Name gag-pol
Organism Human immunodeficiency virus type 1 group M subtype D (isolate Z6) (HIV-1)
Taxonomic Lineage Viruses Riboviria Pararnavirae Artverviricota Revtraviricetes Ortervirales Retroviridae Orthoretrovirinae Lentivirus Human immunodeficiency virus 1 HIV-1 unknown group Human immunodeficiency virus type 1 group M subtype D (isolate Z6) (HIV-1)
Enzyme Sequence IPYNPQSQGVVESMNKELKKIIGQVRDQAEHLKTAVQMAVFIHNFKRKGGIGGYSAGERIIDIIATDIQTKELQKQITKIQNFRVYYRDSRDPIWKGPAKLLWKGEGAVVIQDNSDIKVVPRRKVKIIRDYGKQMAGDDCVASRQDED
Enzyme Length 148
Uniprot Accession Number P04586
Absorption
Active Site
Activity Regulation
Binding Site
Calcium Binding
catalytic Activity
DNA Binding DNA_BIND 83..130; /note=Integrase-type; /evidence=ECO:0000255|PROSITE-ProRule:PRU00506
EC Number 2.7.7.-; 3.1.-.-
Enzyme Function FUNCTION: [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. {ECO:0000250|UniProtKB:P04585}.
Temperature Dependency
PH Dependency
Pathway
nucleotide Binding
Features Beta strand (4); Chain (2); DNA binding (1); Domain (1); Helix (1); Metal binding (1); Non-terminal residue (1)
Keywords 3D-structure;AIDS;DNA integration;DNA recombination;DNA-binding;Endonuclease;Eukaryotic host gene expression shutoff by virus;Eukaryotic host translation shutoff by virus;Host gene expression shutoff by virus;Host-virus interaction;Hydrolase;Lipid-binding;Magnesium;Metal-binding;Nuclease;Nucleotidyltransferase;Transferase;Viral genome integration;Virus entry into host cell
Interact With
Induction
Subcellular Location
Modified Residue
Post Translational Modification PTM: Specific enzymatic cleavages by the viral protease yield mature proteins. {ECO:0000250}.
Signal Peptide
Structure 3D NMR spectroscopy (2)
Cross Reference PDB 1IHV; 1IHW;
Mapped Pubmed ID -
Motif
Gene Encoded By
Mass 16,840
Kinetics
Metal Binding METAL 12; /note=Magnesium; catalytic; for integrase activity; /evidence=ECO:0000250|UniProtKB:P04585
Rhea ID
Cross Reference Brenda