Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Foamy Virus Capsids Require the Cognate Envelope Protein for Particle Export

1 Apr 1999

Abstract excerpt

Unlike other subclasses of the Retroviridae the Spumavirinae, its prototype member being the so-called human foamy virus (HFV), require the expression of the envelope (Env) glycoprotein for viral particle egress. Both the murine leukemia virus (MuLV) Env and the vesicular stomatitis virus G protein, which efficiently pseudotype other retrovirus capsids, were not able to support export of HFV particles. Analysis...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to HIV Research and Treatment
Share to Viral Infections and Immunology Research
Share to Virus-based gene therapy research

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10074106
DOI: 10.1128/jvi.73.4.2613-2621.1999

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Foamy Virus Capsids Require the Cognate Envelope Protein for Particle ExportPMID 10074106Read ↗

Foamy Virus Budding and ReleaseSemantic proximity Read ↗

Characterization of Prototype Foamy Virus Gag Late Assembly Domain Motifs and Their Role in Particle Egress and InfectivitySemantic proximity Read ↗

The Roles of Pol and Env in the Assembly Pathway of Human Foamy VirusSemantic proximity Read ↗

Efficient pseudotyping of murine leukemia virus particles with chimeric human foamy virus envelope proteins.Semantic proximity Read ↗

Mutations in the amino terminus of foamy virus Gag disrupt morphology and infectivity but do not target assembly.Semantic proximity Read ↗

Replication-competent hybrids between murine leukemia virus and foamy virus.Semantic proximity Read ↗

Structures of the Foamy virus fusion protein reveal an unexpected link with the F protein of paramyxo- and pneumovirusesSemantic proximity Read ↗

Correct capsid assembly mediated by a conserved YXXLGL motif in prototype foamy virus Gag is essential for infectivity and reverse transcription of the viral genome.Semantic proximity Read ↗

Human Foamy Virus Replication: A Pathway Distinct from That of Retroviruses and HepadnavirusesSemantic proximity Read ↗

Mutagenesis of N-terminal residues of feline foamy virus Gag reveals entirely distinct functions during capsid formation, particle assembly, Gag processing and budding.Semantic proximity Read ↗

Analysis of Prototype Foamy Virus particle-host cell interaction with autofluorescent retroviral particlesSemantic proximity Read ↗

Novel Functions of Prototype Foamy Virus Gag Glycine- Arginine-Rich Boxes in Reverse Transcription and Particle MorphogenesisSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.