GO Term |
---|
endopeptidase activity |
exopeptidase activity |
tripeptidyl-peptidase activity |
actin binding |
carboxypeptidase activity |
metalloendopeptidase activity |
metallopeptidase activity |
calmodulin binding |
peptidyl-dipeptidase activity |
zinc ion binding |
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:0060303 | complement component 9 deficiency | |
DOID:0060319 | cardiac arrest | |
DOID:0060444 | granular corneal dystrophy 2 | |
DOID:0060550 | ablepharon macrostomia syndrome | |
DOID:0060600 | obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum | |
DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | |
DOID:0060656 | autosomal recessive congenital ichthyosis 1 | |
DOID:0060672 | Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | |
DOID:0060674 | catecholaminergic polymorphic ventricular tachycardia | |
DOID:0060675 | catecholaminergic polymorphic ventricular tachycardia 1 |
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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