Gene Gene information from NCBI Gene database.
Entrez ID 3416
Gene name Insulin degrading enzyme
Gene symbol IDE
Synonyms (NCBI Gene)
INSULYSIN
Chromosome 10
Chromosome location 10q23.33
Summary This gene encodes a zinc metallopeptidase that degrades intracellular insulin, and thereby terminates insulins activity, as well as participating in intercellular peptide signalling by degrading diverse peptides such as glucagon, amylin, bradykinin, and k
miRNA miRNA information provided by mirtarbase database.
446
miRTarBase ID miRNA Experiments Reference
MIRT025720 hsa-miR-7-5p Microarray 17612493
MIRT025720 hsa-miR-7-5p Microarray 19073608
MIRT675952 hsa-miR-3529-3p HITS-CLIP 23824327
MIRT623645 hsa-miR-6890-3p HITS-CLIP 23824327
MIRT623644 hsa-miR-6736-3p HITS-CLIP 23824327
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
NRF1 Activation 22870279
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
94
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0001540 Function Amyloid-beta binding IEA
GO:0001618 Function Virus receptor activity IEA
GO:0003824 Function Catalytic activity IEA
GO:0004175 Function Endopeptidase activity IDA 20364150
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
146680 5381 ENSG00000119912
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P14735
Protein name Insulin-degrading enzyme (EC 3.4.24.56) (Abeta-degrading protease) (Insulin protease) (Insulinase) (Insulysin)
Protein function Plays a role in the cellular breakdown of insulin, APP peptides, IAPP peptides, natriuretic peptides, glucagon, bradykinin, kallidin, and other peptides, and thereby plays a role in intercellular peptide signaling (PubMed:10684867, PubMed:170512
PDB 2G47 , 2G48 , 2G49 , 2G54 , 2G56 , 2JBU , 2JG4 , 2WBY , 2WC0 , 2WK3 , 2YPU , 3CWW , 3E4A , 3E4Z , 3E50 , 3H44 , 3HGZ , 3N56 , 3N57 , 3OFI , 3QZ2 , 4DTT , 4DWK , 4GS8 , 4GSC , 4GSF , 4IFH , 4IOF , 4LTE , 4M1C , 4NXO , 4PES , 4PF7 , 4PF9 , 4PFC , 4QIA , 4RAL , 4RE9 , 5CJO , 5UOE , 5WOB , 6B3Q , 6B70 , 6B7Y , 6B7Z , 6BF6 , 6BF7 , 6BF8 , 6BF9 , 6BFC , 6BYZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00675 Peptidase_M16 74 212 Insulinase (Peptidase family M16) Family
PF05193 Peptidase_M16_C 237 417 Peptidase M16 inactive domain Domain
PF16187 Peptidase_M16_M 422 703 Middle or third domain of peptidase_M16 Family
PF05193 Peptidase_M16_C 706 889 Peptidase M16 inactive domain Domain
Tissue specificity TISSUE SPECIFICITY: Detected in brain and in cerebrospinal fluid (at protein level). {ECO:0000269|PubMed:9830016}.
Sequence
MRYRLAWLLHPALPSTFRSVLGARLPPPERLCGFQKKTYSKMNNPAIKRIGNHITKSPED
KREYRGLELANGIKVLLISDPTTDKSSAALDVHIGSLSDPPNIAGLSHFCEHMLFLGTKK
YPKENEYSQFLSEHAGSSNAFTSGEHTNYYFDVSHEHLEGALDRFAQFFLCPLFDESCKD
REVNAVDSEHEKNVMNDAWRLFQLEKATGNPK
HPFSKFGTGNKYTLETRPNQEGIDVRQE
LLKFHSAYYSSNLMAVCVLGRESLDDLTNLVVKLFSEVENKNVPLPEFPEHPFQEEHLKQ
LYKIVPIKDIRNLYVTFPIPDLQKYYKSNPGHYLGHLIGHEGPGSLLSELKSKGWVNTLV
GGQKEGARGFMFFIINVDLTEEGLLHVEDIILHMFQYIQKLRAEGPQEWVFQECKDL
NAV
AFRFKDKERPRGYTSKIAGILHYYPLEEVLTAEYLLEEFRPDLIEMVLDKLRPENVRVAI
VSKSFEGKTDRTEEWYGTQYKQEAIPDEVIKKWQNADLNGKFKLPTKNEFIPTNFEILPL
EKEATPYPALIKDTAMSKLWFKQDDKFFLPKACLNFEFFSPFAYVDPLHCNMAYLYLELL
KDSLNEYAYAAELAGLSYDLQNTIYGMYLSVKGYNDKQPILLKKIIEKMATFEIDEKRFE
IIKEAYMRSLNNFRAEQPHQHAMYYLRLLMTEVAWTKDELKEA
LDDVTLPRLKAFIPQLL
SRLHIEALLHGNITKQAALGIMQMVEDTLIEHAHTKPLLPSQLVRYREVQLPDRGWFVYQ
QRNEVHNNCGIEIYYQTDMQSTSENMFLELFCQIISEPCFNTLRTKEQLGYIVFSGPRRA
NGIQGLRFIIQSEKPPHYLESRVEAFLITMEKSIEDMTEEAFQKHIQAL
AIRRLDKPKKL
SAECAKYWGEIISQQYNFDRDNTEVAYLKTLTKEDIIKFYKEMLAVDAPRRHKVSVHVLA
REMDSCPVVGEFPCQNDINLSQAPALPQPEVIQNMTEFKRGLPLFPLVKPHINFMAAKL
Sequence length 1019
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Virion - Herpesvirus
Alzheimer disease
  Ub-specific processing proteases
Peroxisomal protein import
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Likely benign rs201349668 RCV005928964
Sarcoma Likely benign rs201349668 RCV005928965
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
AA amyloidosis Associate 17653279, 18317569, 33865867
Alzheimer Disease Inhibit 12507914
Alzheimer Disease Associate 17244626, 17496198, 17613531, 18813847, 19019493, 19896952, 20098734, 20142614, 20663017, 20724036, 21185309, 21731745, 21992747, 22107728, 23036584
View all (12 more)
Amyloid angiopathy Associate 19019493
Amyotrophic Lateral Sclerosis Associate 27244217
Brain Infarction Associate 23076436
Breast Neoplasms Associate 18813847
Carcinogenesis Associate 25945652
Central Nervous System Neoplasms Stimulate 23188819
Cognition Disorders Associate 24660790, 28050343