RANGAP1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRANGAP1, Fug1, RANGAP, SD, Ran GTPase activating protein 1
External IDsOMIM: 602362; MGI: 103071; HomoloGene: 55700; GeneCards: RANGAP1; OMA:RANGAP1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001278651
NM_002883
NM_001317930

NM_001146174
NM_011241
NM_001358622

RefSeq (protein)

NP_001265580
NP_001304859
NP_002874

NP_001139646
NP_035371
NP_001345551

Location (UCSC)Chr 22: 41.24 – 41.29 MbChr 15: 81.59 – 81.63 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Ran GTPase-activating protein 1 is an enzyme that in humans is encoded by the RANGAP1 gene.[5][6]

Function

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RanGAP1, is a homodimeric 65-kD polypeptide that specifically induces the GTPase activity of RAN, but not of RAS by over 1,000-fold. RanGAP1 is the immediate antagonist of RCC1, a regulator molecule that keeps RAN in the active, GTP-bound state. The RANGAP1 gene encodes a 587-amino acid polypeptide. The sequence is unrelated to that of GTPase activators for other RAS-related proteins, but is 88% identical to Rangap1 (Fug1), the murine homolog of yeast Rna1p. RanGAP1 and RCC1 control RAN-dependent transport between the nucleus and cytoplasm. RanGAP1 is a key regulator of the RAN GTP/GDP cycle.[6]

Interactions

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RanGAP1 is a trafficking protein which helps transport other proteins from the cytoplasm to the nucleus. Small ubiquitin-related modifier needs to be associated with it before it can be localized at the nuclear pore.[7]

RANGAP1 has been shown to interact with:

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000100401Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022391Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Bischoff FR, Krebber H, Kempf T, Hermes I, Ponstingl H (Apr 1995). "Human RanGTPase-activating protein RanGAP1 is a homologue of yeast Rna1p involved in mRNA processing and transport". Proc Natl Acad Sci U S A. 92 (5): 1749–53. Bibcode:1995PNAS...92.1749B. doi:10.1073/pnas.92.5.1749. PMC 42597. PMID 7878053.
  6. ^ a b "Entrez Gene: RANGAP1 Ran GTPase activating protein 1".
  7. ^ Hochstrasser M (2000). "Biochemistry. All in the ubiquitin family". Science. 289 (5479): 563–4. doi:10.1126/science.289.5479.563. PMID 10939967. S2CID 32469429.
  8. ^ Hillig RC, Renault L, Vetter IR, Drell T, Wittinghofer A, Becker J (Jun 1999). "The crystal structure of rna1p: a new fold for a GTPase-activating protein". Mol. Cell. 3 (6): 781–91. doi:10.1016/S1097-2765(01)80010-1. PMID 10394366.
  9. ^ Becker J, Melchior F, Gerke V, Bischoff FR, Ponstingl H, Wittinghofer A (May 1995). "RNA1 encodes a GTPase-activating protein specific for Gsp1p, the Ran/TC4 homologue of Saccharomyces cerevisiae". J. Biol. Chem. 270 (20): 11860–5. doi:10.1074/jbc.270.20.11860. PMID 7744835.
  10. ^ Bischoff FR, Klebe C, Kretschmer J, Wittinghofer A, Ponstingl H (Mar 1994). "RanGAP1 induces GTPase activity of nuclear Ras-related Ran". Proc. Natl. Acad. Sci. U.S.A. 91 (7): 2587–91. Bibcode:1994PNAS...91.2587B. doi:10.1073/pnas.91.7.2587. PMC 43414. PMID 8146159.
  11. ^ Ewing RM, Chu P, Elisma F, Li H, Taylor P, Climie S, McBroom-Cerajewski L, Robinson MD, O'Connor L, Li M, Taylor R, Dharsee M, Ho Y, Heilbut A, Moore L, Zhang S, Ornatsky O, Bukhman YV, Ethier M, Sheng Y, Vasilescu J, Abu-Farha M, Lambert JP, Duewel HS, Stewart II, Kuehl B, Hogue K, Colwill K, Gladwish K, Muskat B, Kinach R, Adams SL, Moran MF, Morin GB, Topaloglou T, Figeys D (2007). "Large-scale mapping of human protein-protein interactions by mass spectrometry". Mol. Syst. Biol. 3: 89. doi:10.1038/msb4100134. PMC 1847948. PMID 17353931.
  12. ^ Tatham MH, Kim S, Yu B, Jaffray E, Song J, Zheng J, Rodriguez MS, Hay RT, Chen Y (Aug 2003). "Role of an N-terminal site of Ubc9 in SUMO-1, -2, and -3 binding and conjugation". Biochemistry. 42 (33): 9959–69. doi:10.1021/bi0345283. PMID 12924945.
  13. ^ Knipscheer P, Flotho A, Klug H, Olsen JV, van Dijk WJ, Fish A, Johnson ES, Mann M, Sixma TK, Pichler A (Aug 2008). "Ubc9 sumoylation regulates SUMO target discrimination". Mol. Cell. 31 (3): 371–82. doi:10.1016/j.molcel.2008.05.022. PMID 18691969.

Further reading

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📚 Artikel Terkait di Wikipedia

UBE2I

ETS1, FHIT, IPO13, MAP3K1 and MITF, P53, PIAS1, PIAS2, RAD51, RANBP2, RANGAP1, SAE2, SALL1, SUMO1, TCF3, TNFRSF1A, TOP1, and WT1. GRCh38: Ensembl release

SUMO1

modification modulates the partitioning of the Ran-GTPase-activating protein RanGAP1 between the cytosol and the nuclear pore complex". The Journal of Cell

SUMO protein

altered localization and binding partners. The SUMO-1 modification of RanGAP1 (the first identified SUMO substrate) leads to its trafficking from cytosol

P53

conjugation revealed by a complex between ubiquitin-conjugating enzyme Ubc9 and RanGAP1". Cell. 108 (3): 345–56. Bibcode:2002Cell..108..345B. doi:10.1016/S0092-8674(02)00630-X

22q13 deletion syndrome

C22orf46 NHP2L1 XRCC6 DESI1 PMM1 CSDC2 POLR3H ACO2 PHF5A TOB2 TEF ZC3H7B RANGAP1 CHADL L3MBTL2 EP300 RBX1 DNAJB7 XPNPEP3 ST13 SLC25A17 MCHR1 MKL1 SGSM3

FAM76A

(January 1997). "A small ubiquitin-related polypeptide involved in targeting RanGAP1 to nuclear pore complex protein RanBP2". Cell. 88 (1): 97–107. doi:10

Kinetochore

anchor, other components such as EB1, APC and proteins in the Ran pathway (RanGap1 and RanBP2) associate to kinetochores only when MTs are anchored. This

List of human protein-coding genes 6

13404 RANBP10 HGNC:29285; Q6VN20 13405 RANBP17 HGNC:14428; Q9H2T7 13406 RANGAP1 HGNC:9854; P46060 13407 RANGRF HGNC:17679; Q9HD47 13408 RAP1A HGNC:9855;