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P15834 (VIF_HV2D2) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 67. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (1) | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein namesRecommended name:
Virion infectivity factor

Short name=Vif
Alternative name(s):
Q protein
SOR protein
Gene names
Name:vif
OrganismHuman immunodeficiency virus type 2 subtype B (isolate D205) (HIV-2)
Taxonomic identifier11716 [NCBI]
Taxonomic lineageVirusesRetro-transcribing virusesRetroviridaeOrthoretrovirinaeLentivirusPrimate lentivirus group
Virus hostHomo sapiens (Human) [TaxID: 9606]

Protein attributes

Sequence length216 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Counteracts the innate antiviral activity of APOBEC3G. Forms a complex with host APOBEC3G thus preventing the entry of this lethally hypermutating enzyme into progeny virions. Functions as an adapter molecule, recruiting APOBEC3G to the ubiquitin-proteasome machinery. Targets APOBEC3G for degradation through the assembly with elongin BC complex, CUL5 and RBX1. Binds viral RNA and affects the stability of viral nucleoprotein core. May play a role in viral morphology By similarity.

Subunit structure

Homomultimer; in vitro and presumably in vivo. Interacts with viral Pr55Gag precursor and human APOBEC3G. The interaction between Vif and APOBEC3G is species-specific, which may play a role in restricting the replication of HIV to humans. Forms an E3 ligase complex by interacting with human CUL5 and elongin BC complex (TCEB1 and TCEB2) By similarity.

Subcellular location

Host cytoplasm By similarity. Host cell membrane; Peripheral membrane protein; Cytoplasmic side By similarity. Virion By similarity. Note: In the cytoplasm, seems to colocalize with intermediate filament vimentin. A fraction is associated with the cytoplasmic side of cellular membranes, presumably via the interaction with Pr55Gag precursor By similarity.

Induction

Expressed late during infection in a Rev-dependent manner.

Domain

The BC-like-box motif mediates the interaction with elongin BC complex By similarity.

The HCCH motif (H-x(5)-C-x(18)-C-x(5)-H) mediates the interaction with CUL5 By similarity.

Post-translational modification

Processed in virion by the viral protease By similarity.

Highly phosphorylated on serines and threonines residues By similarity.

Polyubiquitinated and degraded by the proteasome in the presence of APOBEC3G By similarity.

Miscellaneous

Required for replication in 'nonpermissive' cells, including primary T-cells, macrophages and certain T-cell lines, but is dispensable for replication in 'permissive' cell lines, such as 293T cells. In nonpermissive cells, Vif-defective viruses can produce virions, but they fail to complete reverse transcription and cannot successfully infect new cells.

Vif-defective viruses show catastrophic failure in reverse transcription due to APOBEC-induced mutations that initiate a DNA base repair pathway and compromise the structural integrity of the ssDNA. In the absence of Vif, the virion is morphologically abnormal.

Sequence similarities

Belongs to the primate lentivirus group Vif protein family.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 216216Virion infectivity factor
PRO_0000085319

Regions

Region154 – 16714Multimerization By similarity
Motif110 – 14132HCCH motif By similarity
Motif147 – 15610BC-box-like motif By similarity

Amino acid modifications

Modified residue981Phosphothreonine; by host MAP4K1 By similarity
Modified residue1471Phosphoserine; by host By similarity

Sequences

Sequence LengthMass (Da)Tools
P15834 [UniParc].

Last modified April 1, 1990. Version 1.
Checksum: AA4624F121CB6BE6

FASTA21625,165
        10         20         30         40         50         60 
MEEEKDWIVV PTWRIPGRLE RWHSLIKYLK YRTGELQQVS YVPHHKVGWA WWTCSRIIFP 

        70         80         90        100        110        120 
LNKGAWLEVQ GYWNLTPERG FLSSYAVRLT WYERNFYTDV TPDVADQLLH GSYFSCFSAN 

       130        140        150        160        170        180 
EVRRAIRGEK ILSYCNYPSA HEGQVPSLQF LALRVVQEGK NGSQGESATR KQRRRNSRRS 

       190        200        210 
IRLARKNNNR AQQGSGQPFA PRTYFPGLAE VLGILA 

« Hide

References

[1]"A highly divergent HIV-2-related isolate."
Dietrich U., Adamski M., Kreutz R., Seipp A., Kuehnel H., Ruebsamen-Waigmann H.
Nature 342:948-950(1989) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
X61240 Genomic DNA. No translation available.
PIRS08437.

3D structure databases

ModBaseSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Family and domain databases

InterProIPR000475. Viral_infect.
[Graphical view]
PfamPF00559. Vif. 1 hit.
[Graphical view]
PRINTSPR00349. VIRIONINFFCT.
ProtoNetSearch...

Entry information

Entry nameVIF_HV2D2
AccessionPrimary (citable) accession number: P15834
Entry history
Integrated into UniProtKB/Swiss-Prot: April 1, 1990
Last sequence update: April 1, 1990
Last modified: April 3, 2013
This is version 67 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programViral Protein Annotation Program

Relevant documents

SIMILARITY comments

Index of protein domains and families