PRSS3 - serine protease 3 Gene

Also Known as T9; MTG; TRY3; TRY4; PRSS4

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 5646

About PRSS3

Cytogenetic location: 9p13.3 Genomic coordinates (GRCh38): 9:33,750,679-33,799,231 (from NCBI)

This gene has 7 transcripts (splice variants), 474 orthologues and 3 paralogues. Restricted expression toward pancreas (RPKM 3091.3).

Summary

This gene encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is expressed in the brain and pancreas and is resistant to common trypsin inhibitors. It is active on peptide linkages involving the carboxyl group of lysine or arginine. This gene is localized to the locus of T cell receptor beta variable orphans on chromosome 9. Four transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2010]

PRSS3 Products (4)

mRNA Protein Name
NM_001197097.3 NP_001184026.3 trypsin-3 isoform 3 preproprotein
NM_001197098.1 NP_001184027.1 trypsin-3 isoform 4 preproprotein
NM_002771.4 NP_002762.3 trypsin-3 isoform 2 preproprotein
NM_007343.4 NP_031369.3 trypsin-3 isoform 1 preproprotein
Molecular Function GO Annotation Evidence 参考文献 由来
enables calcium ion binding IDA
IDA: Inferred from direct assay
6698368 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
6698368 GOA
enables serine-type endopeptidase activity IDA
IDA: Inferred from direct assay
6698368 GOA
enables serine-type peptidase activity IDA
IDA: Inferred from direct assay
9099703 GOA
Biological Process GO Annotation Evidence 参考文献 由来
involved in endothelial cell migration IMP
IMP: Inferred from mutant phenotype
15313892 GOA
involved in proteolysis IDA
IDA: Inferred from direct assay
6698368 GOA
involved in zymogen activation IDA
IDA: Inferred from direct assay
6698368 GOA
Cellular Component GO Annotation Evidence 参考文献 由来
located in extracellular space IDA
IDA: Inferred from direct assay
6698368 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PRSS3 Protein Structure

Trypsin

Trypsin: Trypsin (81 - 296)

  • 0
  • 100
  • 200
  • 304 a.a.
Protein Preferred Names Protein Names

trypsin-3

  • brain trypsinogen

Recombinant PRSS3 Proteins

製品番号 製品名 アクセッション番号 純度
HY-P71456 PRSS3/Trypsin-3 Protein, Human (His) P35030-1 (I81-N303) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P75985 PRSS3/Trypsin-3 Protein, Human (HEK293, His) P35030-3 (V16-S247) ≥ 95%, as determined by reducing SDS-PAGE.

関連疾患

Diseases Alias
Thyroiditis
  • Inflammation Of Thyroid

  • Thyroiditis Nos

Hashimoto Thyroiditis
  • Autoimmune Thyroiditis

  • Hashimoto Struma

  • Hashimoto'S Thyroiditis

  • Chronic Lymphocytic Thyroiditis

  • Lymphocytic Thyroiditis

  • Hashimoto Disease

  • Ht

  • Hashimoto'S Disease

  • Hashimoto'S Syndrome

  • Hypothyroidism, Autoimmune

  • Autoimmune Chronic Lymphocytic Thyroiditis

  • Chronic Lymphocytic Thyroiditides

  • Hashimoto Syndrome

  • Hashimotos Thyroiditis

  • Hashimoto Thyroiditis, Susceptibility To

  • Thyroiditis, Autoimmune

  • Lymphomatous Thyroiditis

  • Lymphoid Thyroiditis

  • Chronic Lymphadenoid Thyroiditis

  • Autoimmune Lymphocytic Chronic Thyroiditis

  • Goitre Lymphomatosa

  • Hashitoxicosis

  • Hashimoto Hypothyroidism

  • Lymphadenoid Goitre

  • Struma Lymphomatosa

  • Hyperthyroidism With Hashimoto Disease

  • Hashimoto Thyrotoxicosis

  • Thyrotoxicosis Due To Hashimoto Thyroiditis

  • Struma Lymphomatosis

  • Lymphadenoid Struma

Pancreatitis
  • Mumps Pancreatitis

Pancreatitis, Hereditary
  • Hereditary Pancreatitis

  • Chronic Pancreatitis

  • Hereditary Chronic Pancreatitis

  • Hp

  • Pancreatitis, Chronic, Susceptibility To

  • PCTT

  • Hpc

  • Pancreatitis, Chronic

  • Pancreatitis, Chronic, Protection Against

  • Autosomal Dominant Hereditary Pancreatitis

  • Familial Pancreatitis

  • Cp

  • Pancreatitis Hereditary

Autoimmune Disease Of Endocrine System
Celiac Disease 1
  • Celiac Disease

  • Coeliac Disease

  • Celiac Sprue

  • Celiac Disease, Susceptibility To

  • Gluten-Sensitive Enteropathy

  • Nontropical Sprue

  • Sprue

  • CELIAC1

  • Celiac Disease, Susceptibility To, 1

  • Celiac Sprue 1

  • Celiac Sprue, Susceptibility To, 1

  • Gluten-Sensitive Enteropathy 1

  • Gluten-Sensitive Enteropathy, Susceptibility To, 1

  • Idiopathic Steatorrhea

  • Cœliac Disease

  • Gluten Intolerance

  • Gluten-Induced Enteropathy

  • Gluten Enteropathy

  • Celiac Disease, Susceptibility To, Type 1

  • Childhood Celiac Disease

  • Coeliac Rickets

  • Gee Disease

  • Gee-Herter Disease

  • Heubner-Herter Disease

  • Idiopathic Steatorrhoea

  • Thaysen'S Disease

  • Herter Gee Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

生物種 Symbol 由来 ID
Rattus norvegicus PRSS3 RGD RGD:1311446
Others PRSS3 NCBI