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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Dipeptidase 1
Summary
- UniProt ID
- P16444
- Gene Symbol
-
- DPEP1
- MDP
- RDP
- Organism
- Homo sapiens (human)
External Links
- GlycoProtDB
- GPDB0011574
- GlyConnect
- GlyGen
- P16444
- PubChem
- P16444
- The Human Metabolome Database
- HMDBP02684
- The O-GlcNAc Database
- P16444
- RaftProt
- P16444
Annotation
- Keyword
-
- 3D-structure
- Cell membrane
- Cell projection
- Dipeptidase
- Direct protein sequencing
- Disulfide bond
- GPI-anchor
- Lipid metabolism
- Metal-binding
- Metalloprotease
- Reference proteome
- Signal
- Zinc
- Gene Ontology (GO)
| GO Term |
|---|
| negative regulation of cysteine-type endopeptidase activity involved in apoptotic process |
| glutathione catabolic process |
| cellular response to xenobiotic stimulus |
| lactam catabolic process |
| leukotriene D4 catabolic process |
| GO Term |
|---|
| extracellular space |
| plasma membrane |
| cell junction |
| extracellular exosome |
| apical plasma membrane |
| microvillus membrane |
| apical part of cell |
| nucleoplasm |
| side of membrane |
Sequence
MWSGWWLWPLVAVCTADFFRDEAERIMRDSPVIDGHNDLPWQLLDMFNNRLQDERANLTTLAGTHTNIPKLRAGFVGGQFWSVYTPCDTQNKDAVRRTLEQMDVVHRMCRMYPETFLYVTSSAGIRQAFREGKVASLIGVEGGHSIDSSLGVLRALYQLGMRYLTLTHSCNTPWADNWLVDTGDSEPQSQGLSPFGQRVVKELNRLGVLIDLAHVSVATMKATLQLSRAPVIFSHSSAYSVCASRRNVPDDVLRLVKQTDSLVMVNFYNNYISCTNKANLSQVADHLDHIKEVAGARAVGFGGDFDGVPRVPEGLEDVSKYPDLIAELLRRNWTEAEVKGALADNLLRVFEAVEQASNLTQAPEEEPIPLDQLGGSCRTHYGYSSGASSLHRHWGLLLASLAPLVLCLSLL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 332 |
|
|
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Aflatoxin activation and detoxification | Homo sapiens |
| LTC4-CYSLTR mediated IL4 production | Homo sapiens |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | |
| DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R | |
| DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S | |
| DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | |
| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | |
| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | |
| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | |
| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | |
| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K |
