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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Xylosyltransferase 2
Summary
- UniProt ID
- Q9H1B5
- Gene Symbol
-
- XYLT2
- XT2
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q9H1B5
- The Human Metabolome Database
- HMDBP03144
- RaftProt
- Q9H1B5
Annotation
- Keyword
-
- Alternative splicing
- Disease variant
- Disulfide bond
- Glycoprotein
- Glycosyltransferase
- Golgi apparatus
- Magnesium
- Manganese
- Metal-binding
- Reference proteome
- Secreted
- Signal-anchor
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| Golgi membrane |
| extracellular space |
| GO Term |
|---|
| manganese ion binding |
| protein xylosyltransferase activity |
| magnesium ion binding |
Sequence
MVASARVQKLVRRYKLAIATALAILLLQGLVVWSFSGLEEDEAGEKGRQRKPRPLDPGEGSKDTDSSAGRRGSTGRRHGRWRGRAESPGVPVAKVVRAVTSRQRASRRVPPAPPPEAPGRQNLSGAAAGEALVGAAGFPPHGDTGSVEGAPQPTDNGFTPKCEIVGKDALSALARASTKQCQQEIANVVCLHQAGSLMPKAVPRHCQLTGKMSPGIQWDESQAQQPMDGPPVRIAYMLVVHGRAIRQLKRLLKAVYHEQHFFYIHVDKRSDYLHREVVELAQGYDNVRVTPWRMVTIWGGASLLRMYLRSMRDLLEVPGWAWDFFINLSATDYPTRTNEELVAFLSKNRDKNFLKSHGRDNSRFIKKQGLDRLFHECDSHMWRLGERQIPAGIVVDGGSDWFVLTRSFVEYVVYTDDPLVAQLRQFYTYTLLPAESFFHTVLENSLACETLVDNNLRVTNWNRKLGCKCQYKHIVDWCGCSPNDFKPQDFLRLQQVSRPTFFARKFESTVNQEVLEILDFHLYGSYPPGTPALKAYWENTYDAADGPSGLSDVMLTAYTAFARLSLHHAATAAPPMGTPLCRFEPRGLPSSVHLYFYDDHFQGYLVTQAVQPSAQGPAETLEMWLMPQGSLKLLGRSDQASRLQSLEVGTDWDPKERLFRNFGGLLGPLDEPVAVQRWARGPNLTATVVWIDPTYVVATSYDITVDTETEVTQYKPPLSRPLRPGPWTVRLLQFWEPLGETRFLVLPLTFNRKLPLRKDDASWLHAGPPHNEYMEQSFQGLSSILNLPQPELAEEAAQRHTQLTGPALEAWTDRELSSFWSVAGLCAIGPSPCPSLEPCRLTSWSSLSPDPKSELGPVKADGRLR
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 327 | N-linked (GlcNAc...) asparagine |
|
||
| 564 |
|
|||
| 565 |
|
|||
| 567 |
|
|||
| 571 |
|
|||
| 683 | N-linked (GlcNAc...) asparagine |
|
||
| 777 |
|
|||
| 782 |
|
|||
| 783 |
|
G57321FI
G43417UB
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110844 | xeroderma pigmentosum group C | |
| DOID:0110845 | xeroderma pigmentosum group D | |
| DOID:0110846 | xeroderma pigmentosum group E | |
| DOID:0110847 | xeroderma pigmentosum variant type | |
| DOID:0110848 | xeroderma pigmentosum group F | |
| DOID:0110849 | xeroderma pigmentosum group G | |
| DOID:0110850 | xeroderma pigmentosum group B | |
| DOID:0111135 | congenital generalized lipodystrophy type 1 | |
| DOID:0111136 | congenital generalized lipodystrophy type 2 | |
| DOID:0111137 | congenital generalized lipodystrophy type 3 |
