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

Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.

Journal of virology - 1 May 2002

Kuo Lili, Masters Paul S

Abstract excerpt

The coronavirus membrane (M) protein is the most abundant virion protein and the key component in viral assembly and morphogenesis. The M protein of mouse hepatitis virus (MHV) is an integral membrane protein with a short ectodomain, three transmembrane segments, and a large carboxy-terminal endodomain facing the interior of the viral envelope. The carboxy terminus of MHV M has previously been shown to be...

Read the complete abstract on PubMed

Topics

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

Share to Membrane Glycoproteins
Share to Murine hepatitis virus
Share to Nucleocapsid

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

Share to Nucleocapsid Proteins

Share to Spike Glycoprotein, Coronavirus

Share to Viral Envelope Proteins

Share to Viral Matrix Proteins

Share to Virus Replication

Source

Open in PubMed Open full text

Identifiers

PMID: 11967315
DOI: 10.1128/jvi.76.10.4987-4999.2002
PMCID: PMC136159

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

Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.PMID 11967315Read ↗

A major determinant for membrane protein interaction localizes to the carboxy-terminal domain of the mouse coronavirus nucleocapsid protein.Semantic proximity Read ↗

Analyses of Coronavirus Assembly Interactions with Interspecies Membrane and Nucleocapsid Protein Chimeras.Semantic proximity Read ↗

Analysis of second-site revertants of a murine coronavirus nucleocapsid protein deletion mutant and construction of nucleocapsid protein mutants by targeted RNA recombination.Semantic proximity Read ↗

Construction of murine coronavirus mutants containing interspecies chimeric nucleocapsid proteins.Semantic proximity Read ↗

Analysis of constructed E gene mutants of mouse hepatitis virus confirms a pivotal role for E protein in coronavirus assembly.Semantic proximity Read ↗

Identification of functionally important negatively charged residues in the carboxy end of mouse hepatitis coronavirus A59 nucleocapsid protein.Semantic proximity Read ↗

Repair and mutagenesis of the genome of a deletion mutant of the coronavirus mouse hepatitis virus by targeted RNA recombination.Semantic proximity Read ↗

The Small Envelope Protein E Is Not Essential for Murine Coronavirus ReplicationSemantic proximity Read ↗

Evolved variants of the membrane protein can partially replace the envelope protein in murine coronavirus assembly.Semantic proximity Read ↗

Coronavirus defective-interfering RNA as an expression vector: the generation of a pseudorecombinant mouse hepatitis virus expressing hemagglutinin-esterase.Semantic proximity Read ↗

Identification of in vivo-interacting domains of the murine coronavirus nucleocapsid protein.Semantic proximity Read ↗

A Hypervariable Region within the 3′ <i>cis</i> -Acting Element of the Murine Coronavirus Genome Is Nonessential for RNA Synthesis but Affects PathogenesisSemantic proximity Read ↗

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