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

p62cdc23 of Saccharomyces cerevisiae: a nuclear tetratricopeptide repeat protein with two mutable domains.

Molecular and cellular biology - 1 Feb 1993

Sikorski R S, Michaud W A, Hieter P

Abstract excerpt

CDC23 is required in Saccharomyces cerevisiae for cell cycle progression through the G2/M transition. The CDC23 gene product contains tandem, imperfect repeats, termed tetratricopeptide repeats, (TPR) units common to a protein family that includes several other nuclear division CDC genes. In this report we have used mutagenesis to probe the functional significance of the TPR units within CDC23. Analysis of...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Base Sequence
Share to Fungal Proteins

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

Share to Genetic Complementation Test

Share to Immunohistochemistry

Share to Molecular Sequence Data

Share to Phenotype

Share to Saccharomyces cerevisiae

Source

Open in PubMed Open full text

Identifiers

PMID: 8423787
DOI: 10.1128/mcb.13.2.1212-1221.1993
PMCID: PMC359006

Genes

CDC23
TPR

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

p62cdc23 of Saccharomyces cerevisiae: a nuclear tetratricopeptide repeat protein with two mutable domains.PMID 8423787Read ↗

Rad24 truncation, coupled with altered telomere structure, promotes cdc13-1 suppression in S. cerevisiae.Semantic proximity Read ↗

Genetic analysis reveals essential and non-essential amino acids within the telomeric DNA-binding interface of Cdc13p.Semantic proximity Read ↗

A genomic screen identifies Dsk2p and Rad23p as essential components of ER-associated degradation.Semantic proximity Read ↗

Identification of the single-strand telomeric DNA binding domain of the Saccharomyces cerevisiae Cdc13 protein.Semantic proximity Read ↗

A double-strand break repair component is essential for S phase completion in fission yeast cell cycling.Semantic proximity Read ↗

Characterization of the Saccharomyces cerevisiae cdc42-1ts allele and new temperature-conditional-lethal cdc42 alleles.Semantic proximity Read ↗

The essential schizosaccharomyces pombe cdc23 DNA replication gene shares structural and functional homology with the Saccharomyces cerevisiae DNA43 (MCM10) gene.Semantic proximity Read ↗

Human CDC23: cDNA cloning, mapping to 5q31, genomic structure, and evaluation as a candidate tumor suppressor gene in myeloid leukemias.Semantic proximity Read ↗

Single site suppressors of a fission yeast temperature-sensitive mutant in cdc48 identified by whole genome sequencing.Semantic proximity Read ↗

Allele-specific suppression of temperature-sensitive mutations of the Saccharomyces cerevisiae RAD52 gene.Semantic proximity Read ↗

Involvement of rhp23, a Schizosaccharomyces pombe homolog of the human HHR23A and Saccharomyces cerevisiae RAD23 nucleotide excision repair genes, in cell cycle control and protein ubiquitination.Semantic proximity Read ↗

Identification of regions critical for the integrity of the TSC1-TSC2-TBC1D7 complex.Semantic proximity Read ↗

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