Homo sapiens Protein: MYO5B | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-3290.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | MYO5B | ||||||||||||||||||
Protein Name | myosin VB | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000285039 | ||||||||||||||||||
InnateDB Gene | IDBG-3288 (MYO5B) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | May be involved in vesicular trafficking via its association with the CART complex. The CART complex is necessary for efficient transferrin receptor recycling but not for EGFR degradation. Required in a complex with RAB11A and RAB11FIP2 for the transport of NPC1L1 to the plasma membrane. Together with RAB11A participates in CFTR trafficking to the plasma membrane and TF (transferrin) recycling in nonpolarized cells. Together with RAB11A and RAB8A participates in epithelial cell polarization. Together with RAB25 regulates transcytosis (By similarity). {ECO:0000250}. | ||||||||||||||||||
Subcellular Localization | |||||||||||||||||||
Disease Associations | Diarrhea 2, with microvillus atrophy (DIAR2) [MIM:251850]: A disease characterized by onset of intractable life-threatening watery diarrhea during infancy. Two forms are recognized: early-onset microvillus inclusion disease with diarrhea beginning in the neonatal period, and late-onset, with first symptoms appearing after 3 or 4 months of life. {ECO:0000269PubMed:18724368}. 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 14 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 |
IPR000048
IQ motif, EF-hand binding site IPR001609 Myosin head, motor domain IPR002710 Dilute IPR009053 Prefoldin IPR018444 Dil domain IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00612
PF00063 PF01843 |
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PRINTS |
PR00193
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PIRSF | |||||||||||||||||||
SMART |
SM00015
SM00242 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9ULV0 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9ULV0 | ||||||||||||||||||
TrEMBL | Q14782 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 4645 | ||||||||||||||||||
UniGene | Hs.720076 | ||||||||||||||||||
RefSeq | NP_001073936 | ||||||||||||||||||
HUGO | HGNC:7603 | ||||||||||||||||||
OMIM | 606540 | ||||||||||||||||||
CCDS | CCDS42436 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB032945 AB290160 AC090227 AC091044 AC092705 AC105224 BC033527 CH471096 L29143 | ||||||||||||||||||
GenPept | AAA20906 AAH33527 BAA86433 BAG06714 EAW62953 EAW62956 | ||||||||||||||||||