Homo sapiens Protein: ALG13 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-240909.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | ALG13 | ||||||||||||||||||
Protein Name | asparagine-linked glycosylation 13 homolog (S. cerevisiae) | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000378260 | ||||||||||||||||||
InnateDB Gene | IDBG-82767 (ALG13) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Isoform 1: Possible multifunctional enzyme with both glycosyltransferase and deubiquitinase activities.Isoform 2: May be involved in protein N-glycosylation, second step of the dolichol-linked oligosaccharide pathway. | ||||||||||||||||||
Subcellular Localization | Isoform 2: Endoplasmic reticulum {ECO:0000305}. Note=Could be recruited to the cytosolic face of the endoplasmic reticulum membrane through its interaction with ALG14. | ||||||||||||||||||
Disease Associations | Congenital disorder of glycosylation 1S (CDG1S) [MIM:300884]: A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N- glycoproteins during embryonic development, differentiation, and maintenance of cell functions. {ECO:0000269PubMed:22492991}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | |||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR002999
Tudor domain IPR003323 Ovarian tumour, otubain IPR007235 Glycosyl transferase, family 28, C-terminal |
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PFAM |
PF00567
PF02338 PF04101 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00333
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9NP73 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9NP73 | ||||||||||||||||||
TrEMBL | D6RE84 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 79868 | ||||||||||||||||||
UniGene | Hs.443061 | ||||||||||||||||||
RefSeq | NP_001093392 | ||||||||||||||||||
HUGO | HGNC:30881 | ||||||||||||||||||
OMIM | 300776 | ||||||||||||||||||
CCDS | CCDS55477 | ||||||||||||||||||
HPRD | 06542 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AF220051 AK026671 AK223154 AK300394 AK302729 AK302890 AK304712 AK312229 AK316306 AK316522 AL049563 AL096764 BC005336 BC117377 BC117379 CH471120 | ||||||||||||||||||
GenPept | AAF67644 AAH05336 AAI17378 AAI17380 BAB15521 BAD96874 BAG35162 BAH13276 BAH13790 BAH13833 BAH14244 BAH14677 BAH14893 CAB89277 CAI43016 CAM28218 CAM28219 CAM28289 EAX02635 | ||||||||||||||||||