Rab19
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Official Full Name
RAB19, member RAS oncogene family -
Synonyms
RAB19;RAB19, member RAS oncogene family;ras-related protein Rab-19;RAB19B;GTP-binding protein RAB19B;OTTHUMP00000212106;OTTHUMP00000212107
Recombinant Proteins
- Mouse
- Rhesus macaque
- Rat
- Chicken
- Human
- E.coli
- Mammalian Cells
- HEK293
- GST
- His
- Non
- His&Fc&Avi
Involved Pathway
Rab19 involved in several pathways and played different roles in them. We selected most pathways Rab19 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with Rab19 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
Rab19 has several biochemical functions, for example, GTP binding,GTPase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by Rab19 itself. We selected most functions Rab19 had, and list some proteins which have the same functions with Rab19. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| GTP binding | NUDT2,LSG1,DIRAS1A,GLUD2,GTPBP6,RAB36,RAB7L1,RAB3AA,GFM2,TUBA1L2 |
| GTPase activity | GNL3,TUBB,RRAS,TUBD1,TUBA8L2,RRAD,ARF4,MX1,EEF1A1A,ARF6 |
Interacting Protein
Rab19 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with Rab19 here. Most of them are supplied by our site. Hope this information will be useful for your research of Rab19.
pi3p
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References
- Gillingham, AK; Sinka, R; et al. Toward a Comprehensive Map of the Effectors of Rab GTPases. DEVELOPMENTAL CELL 31:358-373(2014).
- Schluth-Bolard, C; Labalme, A; et al. Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations. JOURNAL OF MEDICAL GENETICS 50:144-150(2013).
