NUFIP2
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Official Full Name
nuclear fragile X mental retardation protein interacting protein 2 -
Overview
Nuclear fragile X mental retardation-interacting protein 2 is a protein that in humans is encoded by the NUFIP2 gene. -
Synonyms
NUFIP2;nuclear fragile X mental retardation protein interacting protein 2;nuclear fragile X mental retardation-interacting protein 2;82 FIP;182 FIP;FIP 82;KIAA1321;MGC117262;PIG1;FMRP-interacting protein 2;proliferation-inducing gene 1;82-kD FM
Recombinant Proteins
- Mouse
- Rhesus macaque
- Human
- Mammalian Cells
- HEK293
- E.coli
- His
- Non
- His&Fc&Avi
- Myc&DDK
- GST
Involved Pathway
NUFIP2 involved in several pathways and played different roles in them. We selected most pathways NUFIP2 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with NUFIP2 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
Pathway Name | Pathway Related Protein |
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Protein Function
NUFIP2 has several biochemical functions, for example, RNA binding,poly(A) RNA binding,protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by NUFIP2 itself. We selected most functions NUFIP2 had, and list some proteins which have the same functions with NUFIP2. You can find most of the proteins on our site.
Function | Related Protein |
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poly(A) RNA binding | RBM8A,PARP1,FAM103A1,RPLP0,PNO1,ZCRB1,ALDH6A1,MAP4,LIN28B,HSPD1 |
RNA binding | NSUN5B,RBMS3,DHX36,RBM3,HSP90B1,RPL7,NUFIP1,EIF3BA,CWC15,NABP1 |
protein binding | EIF4EBP3,GYPB,CHD2,NFE2L2,DAG1,SETD6,COMMD10,LMX1B,S100A10,ZHX2 |
Interacting Protein
NUFIP2 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 NUFIP2 here. Most of them are supplied by our site. Hope this information will be useful for your research of NUFIP2.
STAT3;CRK;G3BP1;G3BP2;ssdna_dt;RPL10;SUMO3;YBX1;PPP2R2B;IFI16
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References
- Oldenburg, AR; Delbarre, E; et al. Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes. HUMAN MOLECULAR GENETICS 23:1151-1162(2014).
- Davidovic, L; Navratil, V; et al. A metabolomic and systems biology perspective on the brain of the Fragile X syndrome mouse model. GENOME RESEARCH 21:2190-2202(2011).