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Descriptor English: Tripeptidyl-Peptidase 1
Descriptor Spanish: Tripeptidil Peptidasa 1
Descriptor tripeptidil-peptidasa 1
Entry term(s) proteína CLN2
proteína TPP1
tripeptidil-aminopeptidasa I
tripeptidil-peptidasa I
tripeptidil-proteasa I
Scope note: Serina-proteasas lisosómicas que liberan un tripéptido aminoterminal de un polipéptido y escinden péptidos entre residuos hidrófobos. Enzima que en los seres humanos está codificada por el gen TPP1. Interviene en la degradación del colágeno óseo. Las mutaciones de este gen se asocian a LIPOFUSCINOSIS CEROIDE NEURONAL de tipo 2 y a ATAXIA ESPINOCEREBELOSA autosómica recesiva de tipo 7.
Descriptor Portuguese: Tripeptidil-Peptidase 1
Descriptor French: Tripeptidyl-peptidase-1
Entry term(s): 1, Tripeptidyl-Peptidase
CLN2 Protein
I, Tripeptidyl Peptidase
I, Tripeptidyl Protease
I, Tripeptidyl-Peptidase
Peptidase I, Tripeptidyl
Protein, CLN2
Protein, TPP1
TPP1 Protein
Tripeptidyl Aminopeptidase I
Tripeptidyl Peptidase I
Tripeptidyl Protease I
Tripeptidyl-Peptidase I
Tree number(s): D08.811.277.656.350.100.877
D08.811.277.656.350.350.843
D08.811.277.656.959.780
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000091346
Scope note: Lysosomal Serine proteases that release N-terminal tripeptide from a polypeptide and cleave peptides between hydrophobic residues. An enzyme that in humans encoded by the TPP1 gene. It is involved in the degradation of bone collagen. Mutations in this gene are associated with the CEROID LIPOFUSCINOSIS, NEURONAL, 2; and SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE CEROID LIPOFUSCINOSIS, NEURONAL, 2; AND SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Public MeSH Note: 2022; TRIPEPTIDYL-PEPTIDASES 1 was indexed under AMINOPEPTIDASES, DIPEPTIDYL-PEPTIDYL-PEPTIDASES and under SERINE PROTEASES 1995-2021
History Note: 2022 (1993)
DeCS ID: 59867
Unique ID: D000091346
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2022/01/01
Date of Entry: 2021/07/09
Revision Date: 2021/07/01
Tripeptidyl-Peptidase 1 - Preferred
Concept UI M000748625
Scope note Lysosomal Serine proteases that release N-terminal tripeptide from a polypeptide and cleave peptides between hydrophobic residues. An enzyme that in humans encoded by the TPP1 gene. It is involved in the degradation of bone collagen. Mutations in this gene are associated with the CEROID LIPOFUSCINOSIS, NEURONAL, 2; and SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE CEROID LIPOFUSCINOSIS, NEURONAL, 2; AND SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7.
Preferred term Tripeptidyl-Peptidase 1
Entry term(s) 1, Tripeptidyl-Peptidase
CLN2 Protein
I, Tripeptidyl Peptidase
I, Tripeptidyl Protease
I, Tripeptidyl-Peptidase
Peptidase I, Tripeptidyl
Protein, CLN2
Protein, TPP1
TPP1 Protein
Tripeptidyl Aminopeptidase I
Tripeptidyl Peptidase I
Tripeptidyl Protease I
Tripeptidyl-Peptidase I



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