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

Human pepsin 3b peptide map sequence analysis, genotype and hydrophobic nature.

Journal of chromatography - 27 Aug 1993

Jones A T, Keen J N, Roberts N B

Abstract excerpt

Peptides from a Staphylococcus aureus (V8) proteinase digest of human pepsin 3b have been identified by amino acid sequence analysis. Only 137 out of 326 expected residues were detected from the C and N terminal regions of the molecule. Comparison with amino acid sequences derived from nucleotide analysis of three different pepsinogen A genes, identified 2 out of 4 possible substitutions. The presence of valine...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Chemical Phenomena
Share to Chromatography, High Pressure Liquid

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

Share to Genotype

Share to Molecular Sequence Data

Share to Peptide Mapping

Share to Protein Denaturation

Share to Serine Endopeptidases

Source

Identifiers

PMID: 8408429
DOI: 10.1016/s0021-9673(99)87022-8

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.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Human pepsin 3b peptide map sequence analysis, genotype and hydrophobic nature.PMID 8408429Read ↗

Genetic Analysis of Human Chymotrypsin-Like Elastases 3A and 3B (CELA3A and CELA3B) to Assess the Role of Complex Formation between Proelastases and Procarboxypeptidases in Chronic Pancreatitis.Semantic proximity Read ↗

A highly informative polymorphism of the pepsinogen C gene detected by polymerase chain reaction.Semantic proximity Read ↗

Hereditary Carboxypeptidase N deficiency, a clinical situation presenting with urticaria and angioedemaSemantic proximity Read ↗

Haptoglobin polymorphism: a novel genetic risk factor for celiac disease development and its clinical manifestations.Semantic proximity Read ↗

A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.Semantic proximity Read ↗

Absence of pepsinogen A3 gene expression in the gastric mucosa of patients with gastric cancer.Semantic proximity Read ↗

DNA polymorphism and mutations in CPN1, including the genomic basis of carboxypeptidase N deficiency.Semantic proximity Read ↗

Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship.Semantic proximity Read ↗

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