Homo sapiens Protein: LRSAM1 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-85981.7 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | LRSAM1 | ||||||||||||||||||||||
Protein Name | leucine rich repeat and sterile alpha motif containing 1 | ||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000362421 | ||||||||||||||||||||||
InnateDB Gene | IDBG-85979 (LRSAM1) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | E3 ubiquitin-protein ligase that mediates monoubiquitination of TSG101 at multiple sites, leading to inactivate the ability of TSG101 to sort endocytic (EGF receptors) and exocytic (HIV-1 viral proteins) cargos. {ECO:0000269PubMed:15256501}. | ||||||||||||||||||||||
Subcellular Localization | Cytoplasm {ECO:0000269PubMed:15256501}. Note=Displays a punctuate distribution and localizes to a submembranal ring. | ||||||||||||||||||||||
Disease Associations | Charcot-Marie-Tooth disease 2P (CMT2P) [MIM:614436]: An axonal form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies (designated CMT1 when they are dominantly inherited) and primary peripheral axonal neuropathies (CMT2). Neuropathies of the CMT2 group are characterized by signs of axonal degeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy. Nerve conduction velocities are normal or slightly reduced. {ECO:0000269PubMed:20865121, ECO:0000269PubMed:22012984}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | Highly expressed in adult spinal cord motoneurons as well as in fetal spinal cord and muscle tissue. {ECO:0000269PubMed:22012984}. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 51 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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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 |
IPR001611
Leucine-rich repeat IPR001660 Sterile alpha motif domain IPR001841 Zinc finger, RING-type IPR003591 Leucine-rich repeat, typical subtype IPR008731 Phosphotransferase system, enzyme I N-terminal IPR011510 Sterile alpha motif, type 2 IPR013761 Sterile alpha motif/pointed domain IPR021129 Sterile alpha motif, type 1 |
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PFAM |
PF00560
PF13504 PF13855 PF13639 PF14634 PF05524 PF07647 PF00536 |
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PRINTS | |||||||||||||||||||||||
PIRSF | |||||||||||||||||||||||
SMART |
SM00454
SM00184 SM00369 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | Q6UWE0 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-Q6UWE0 | ||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 90678 | ||||||||||||||||||||||
UniGene | Hs.495188 | ||||||||||||||||||||||
RefSeq | NP_001177652 | ||||||||||||||||||||||
HUGO | HGNC:25135 | ||||||||||||||||||||||
OMIM | 610933 | ||||||||||||||||||||||
CCDS | CCDS55347 | ||||||||||||||||||||||
HPRD | 14325 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AK056203 AK056305 AK091589 AL445222 AY358830 BC009239 | ||||||||||||||||||||||
GenPept | AAH09239 AAQ89189 BAB71119 BAB71144 BAC03703 CAH72930 CAH72931 | ||||||||||||||||||||||