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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 |
|---|
| glutathione metabolic process |
| antibiotic metabolic process |
| homocysteine metabolic process |
| negative regulation of cysteine-type endopeptidase activity involved in apoptotic process |
| glutathione catabolic process |
| GO Term |
|---|
| cell junction |
| extracellular exosome |
| apical plasma membrane |
| microvillus membrane |
| apical part of cell |
| nucleoplasm |
| extracellular space |
| plasma membrane |
| 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:0050424 | familial adenomatous polyposis | |
| DOID:0050557 | congenital muscular dystrophy | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050819 | obsolete Matthew-Wood syndrome | |
| DOID:0050835 | generalized dystonia | |
| DOID:0050841 | focal hand dystonia | |
| DOID:0060178 | familial hemiplegic migraine | |
| DOID:0060192 | Crohn's colitis | |
| DOID:0060255 | rippling muscle disease 2 | |
| DOID:0060706 | X-linked lymphoproliferative syndrome 2 |
