Properdin
| GO Term |
|---|
| extracellular region |
| extracellular space |
| specific granule lumen |
| cytoplasmic side of Golgi membrane |
| tertiary granule lumen |
| endoplasmic reticulum lumen |
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 83 | C-linked (Man) tryptophan |
|
||
| 86 | C-linked (Man) tryptophan |
|
||
| 92 | O-linked (Fuc...) threonine |
|
||
| 139 | C-linked (Man) tryptophan |
|
||
| 142 | C-linked (Man) tryptophan |
|
||
| 145 | C-linked (Man) tryptophan |
|
||
| 151 | O-linked (Fuc...) threonine |
|
||
| 196 | C-linked (Man) tryptophan |
|
||
| 199 | C-linked (Man) tryptophan |
|
||
| 202 | C-linked (Man) tryptophan |
|
| Pathway Name | Organism |
|---|---|
| Defective B3GALTL causes PpS | Homo sapiens |
| Neutrophil degranulation | Homo sapiens |
| O-glycosylation of TSR domain-containing proteins | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0111768 | X-linked properdin deficiency |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 8, 2025