Rab escort protein

CHM

Identifiers

CHM, DXS540, GGTA, HSD-32, REP-1, TCD, Rab escort protein 1

External IDs

MGI: 892979 HomoloGene: 334 GeneCards: CHM

Gene ontology
Molecular function	• Rab geranylgeranyltransferase activity • oxidoreductase activity • Rab GTPase binding • GTPase activator activity • GDP-dissociation inhibitor activity
Cellular component	• cytoplasm • Rab-protein geranylgeranyltransferase complex • cytosol
Biological process	• positive regulation of GTPase activity • intracellular protein transport • protein geranylgeranylation • oxidation-reduction process • response to stimulus • visual perception • protein targeting to membrane • regulation of catalytic activity • small GTPase mediated signal transduction • regulation of apoptotic process
Sources:Amigo / QuickGO

RNA expression pattern

More reference expression data

Orthologs

Species

Human

Mouse

Entrez


1121


12662

Ensembl


ENSG00000188419


ENSMUSG00000025531

UniProt


P24386


Q9QXG2

RefSeq (mRNA)


NM_000390 NM_001037312 NM_001145414 NM_001320959


NM_018818

RefSeq (protein)


NP_000381.1 NP_001138886.1 NP_001307888.1


n/a

Location (UCSC)

Chr X: 85.86 – 86.05 Mb

Chr X: 113.04 – 113.19 Mb

PubMed search

^[1]

^[2]

Wikidata

View/Edit Human

View/Edit Mouse

Rab escort protein 1 (REP1) also known as rab proteins geranylgeranyltransferase component A 1 is an enzyme that in humans is encoded by the CHM gene.^[3]^[4]

Function

This gene encodes component A of the RAB geranylgeranyl transferase holoenzyme. In the dimeric holoenzyme, this subunit binds unprenylated Rab GTPases and then presents them to the catalytic Rab GGTase subunit for the geranylgeranyl transfer reaction. Rab GTPases need to be geranylgeranyled on either one or two cysteine residues in their C-terminus to localize to the correct intracellular membrane.^[4]

Interactions

CHM (gene) has been shown to interact with RAB1A,^[5] RAB7A^[6]^[7] and RAB3A.^[5]^[8]

Clinical significance

Mutations in this gene are a cause of choroideremia; also known as tapetochoroidal dystrophy (TCD). This X-linked disease is characterized by progressive dystrophy of the choroid, retinal pigment epithelium and retina.^[4]

References

↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Molloy CM, van de Pol TJ, Brohet RM, Ropers HH, Cremers FP (May 1992). "Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2". Nucleic Acids Res. 20 (6): 1434. doi:10.1093/nar/20.6.1434. PMC 312214. PMID 1373238.
1 2 3 "Entrez Gene: CHM choroideremia (Rab escort protein 1)".
1 2 Cremers FP, Armstrong SA, Seabra MC, Brown MS, Goldstein JL (Jan 1994). "REP-2, a Rab escort protein encoded by the choroideremia-like gene". J. Biol. Chem. 269 (3): 2111–7. PMID 8294464.
↑ Rak A, Pylypenko O, Niculae A, Goody RS, Alexandrov K (Jan 2003). "Crystallization and preliminary X-ray diffraction analysis of monoprenylated Rab7 GTPase in complex with Rab escort protein 1". J. Struct. Biol. 141 (1): 93–5. doi:10.1016/S1047-8477(02)00634-2. PMID 12576024.
↑ Alexandrov K, Simon I, Iakovenko A, Holz B, Goody RS, Scheidig AJ (Apr 1998). "Moderate discrimination of REP-1 between Rab7 x GDP and Rab7 x GTP arises from a difference of an order of magnitude in dissociation rates". FEBS Lett. 425 (3): 460–4. doi:10.1016/S0014-5793(98)00290-7. PMID 9563513.
↑ Pereira-Leal JB, Strom M, Godfrey RF, Seabra MC (Jan 2003). "Structural determinants of Rab and Rab Escort Protein interaction: Rab family motifs define a conserved binding surface". Biochem. Biophys. Res. Commun. 301 (1): 92–7. doi:10.1016/S0006-291X(02)02963-7. PMID 12535645.

Sankila EM, Tolvanen R, van den Hurk JA, Cremers FP, de la Chapelle A (1993). "Aberrant splicing of the CHM gene is a significant cause of choroideremia.". Nat. Genet. 1 (2): 109–13. doi:10.1038/ng0592-109. PMID 1302003.
Merry DE, Jänne PA, Landers JE, Lewis RA, Nussbaum RL (1992). "Isolation of a candidate gene for choroideremia.". Proc. Natl. Acad. Sci. U.S.A. 89 (6): 2135–9. doi:10.1073/pnas.89.6.2135. PMC 48611. PMID 1549574.
van den Hurk JA, van de Pol TJ, Molloy CM, Brunsmann F, Rüther K, Zrenner E, Pinckers AJ, Pawlowitzki IH, Bleeker-Wagemakers EM, Wieringa B (1992). "Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing.". Am. J. Hum. Genet. 50 (6): 1195–202. PMC 1682553. PMID 1598901.
Fodor E, Lee RT, O'Donnell JJ (1991). "Analysis of choroideraemia gene.". Nature. 351 (6328): 614. doi:10.1038/351614b0. PMID 1904992.
Cremers FP, van de Pol DJ, van Kerkhoff LP, Wieringa B, Ropers HH (1990). "Cloning of a gene that is rearranged in patients with choroideraemia.". Nature. 347 (6294): 674–7. doi:10.1038/347674a0. PMID 2215697.
Cremers FP, Sankila EM, Brunsmann F, Jay M, Jay B, Wright A, Pinckers AJ, Schwartz M, van de Pol DJ, Wieringa B (1990). "Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.". Am. J. Hum. Genet. 47 (4): 622–8. PMC 1683797. PMID 2220804.
Donnelly P, Menet H, Fouanon C, Herbert O, Moisan JP, Le Roux MG, Pascal O (1994). "Missense mutation in the choroideremia gene.". Hum. Mol. Genet. 3 (6): 1017. doi:10.1093/hmg/3.6.1017. PMID 7951216.
Alexandrov K, Horiuchi H, Steele-Mortimer O, Seabra MC, Zerial M (1994). "Rab escort protein-1 is a multifunctional protein that accompanies newly prenylated rab proteins to their target membranes.". EMBO J. 13 (22): 5262–73. PMC 395482. PMID 7957092.
van Bokhoven H, van den Hurk JA, Bogerd L, Philippe C, Gilgenkrantz S, de Jong P, Ropers HH, Cremers FP (1995). "Cloning and characterization of the human choroideremia gene.". Hum. Mol. Genet. 3 (7): 1041–6. doi:10.1093/hmg/3.7.1041. PMID 7981670.
Cremers FP, Armstrong SA, Seabra MC, Brown MS, Goldstein JL (1994). "REP-2, a Rab escort protein encoded by the choroideremia-like gene.". J. Biol. Chem. 269 (3): 2111–7. PMID 8294464.
Seabra MC, Brown MS, Goldstein JL (1993). "Retinal degeneration in choroideremia: deficiency of rab geranylgeranyl transferase.". Science. 259 (5093): 377–81. doi:10.1126/science.8380507. PMID 8380507.
Schwartz M, Rosenberg T, van den Hurk JA, van de Pol DJ, Cremers FP (1993). "Identification of mutations in Danish choroideremia families.". Hum. Mutat. 2 (1): 43–7. doi:10.1002/humu.1380020108. PMID 8477262.
Overmeyer JH, Wilson AL, Erdman RA, Maltese WA (1998). "The putative "switch 2" domain of the Ras-related GTPase, Rab1B, plays an essential role in the interaction with Rab escort protein.". Mol. Biol. Cell. 9 (1): 223–35. doi:10.1091/mbc.9.1.223. PMC 25245. PMID 9437002.
Alexandrov K, Simon I, Iakovenko A, Holz B, Goody RS, Scheidig AJ (1998). "Moderate discrimination of REP-1 between Rab7 x GDP and Rab7 x GTP arises from a difference of an order of magnitude in dissociation rates.". FEBS Lett. 425 (3): 460–4. doi:10.1016/S0014-5793(98)00290-7. PMID 9563513.
Raffaniello RD, Raufman JP (1999). "Cytosolic RAB3D is associated with RAB escort protein (REP), not RAB-GDP dissociation inhibitor (GDI), in dispersed chief cells from guinea pig stomach.". J. Cell. Biochem. 72 (4): 540–8. doi:10.1002/(SICI)1097-4644(19990315)72:4<540::AID-JCB9>3.0.CO;2-D. PMID 10022613.
Thomä NH, Iakovenko A, Kalinin A, Waldmann H, Goody RS, Alexandrov K (2001). "Allosteric regulation of substrate binding and product release in geranylgeranyltransferase type II.". Biochemistry. 40 (1): 268–74. doi:10.1021/bi002034p. PMID 11141079.
Syed N, Smith JE, John SK, Seabra MC, Aguirre GD, Milam AH (2001). "Evaluation of retinal photoreceptors and pigment epithelium in a female carrier of choroideremia.". Ophthalmology. 108 (4): 711–20. doi:10.1016/S0161-6420(00)00643-6. PMID 11297488.
Rak A, Reents R, Pylypenko O, Niculae A, Sidorovitch V, Thomä NH, Waldmann H, Schlichting I, Goody RS, Alexandrov K (2002). "Crystallization and preliminary X-ray diffraction analysis of the Rab escort protein-1 in complex with Rab geranylgeranyltransferase.". J. Struct. Biol. 136 (2): 158–61. doi:10.1006/jsbi.2001.4433. PMID 11886217.

External links

GeneReviews/NCBI/NIH/UW entry on Choroideremia
Rab escort protein 1, human at the US National Library of Medicine Medical Subject Headings (MeSH)

Cell signaling: carrier proteins: signal transducing adaptor proteins

JAK-STAT

see JAK-STAT signaling pathway

Growth factor receptor-bound protein

Other

14-3-3 YWHAE YWHAZ Caveolin Cortactin Death-inducing signaling complex Paxillin MYD88 SMAD TRAF TRAF1 TRAF2 TRAF3 TRAF4 TRAF5 TRAF6) BIN1 SH3BP2 LDB3

CHM CHML

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