GO Term |
---|
peptidase activity |
heterocyclic compound binding |
chloride ion binding |
endopeptidase activity |
exopeptidase activity |
tripeptidyl-peptidase activity |
actin binding |
carboxypeptidase activity |
metalloendopeptidase activity |
metallopeptidase activity |
Position | Description |
---|---|
523 | Not glycosylated |
1225 | Not glycosylated |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
368 | N-linked (GlcNAc...) asparagine |
|
||
445 | N-linked (GlcNAc...) asparagine | |||
509 | N-linked (GlcNAc...) asparagine | |||
523 |
|
|||
617 | N-linked (GlcNAc...) asparagine |
|
||
625 |
|
|
||
677 | N-linked (GlcNAc...) asparagine | |||
695 | N-linked (GlcNAc...) (complex) asparagine |
|
||
714 | N-linked (GlcNAc...) (complex) asparagine | |||
760 | N-linked (GlcNAc...) asparagine; partial |
|
Pathway Name | Organism |
---|---|
Metabolism of Angiotensinogen to Angiotensins | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | |
DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | |
DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | |
DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G | |
DOID:0110282 | autosomal recessive limb-girdle muscular dystrophy type 2H | |
DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | |
DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024