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ANR27_HUMAN
ID   ANR27_HUMAN             Reviewed;        1050 AA.
AC   Q96NW4; Q71MF5; Q86UC3; Q8ND80; Q9H0I4;
DT   06-FEB-2007, integrated into UniProtKB/Swiss-Prot.
DT   06-FEB-2007, sequence version 2.
DT   03-AUG-2022, entry version 156.
DE   RecName: Full=Ankyrin repeat domain-containing protein 27;
DE   AltName: Full=VPS9 domain-containing protein;
GN   Name=ANKRD27; ORFNames=PP12899;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANTS GLY-657 AND ARG-761.
RC   TISSUE=Testis;
RX   PubMed=11230166; DOI=10.1101/gr.gr1547r;
RA   Wiemann S., Weil B., Wellenreuther R., Gassenhuber J., Glassl S.,
RA   Ansorge W., Boecher M., Bloecker H., Bauersachs S., Blum H., Lauber J.,
RA   Duesterhoeft A., Beyer A., Koehrer K., Strack N., Mewes H.-W.,
RA   Ottenwaelder B., Obermaier B., Tampe J., Heubner D., Wambutt R., Korn B.,
RA   Klein M., Poustka A.;
RT   "Towards a catalog of human genes and proteins: sequencing and analysis of
RT   500 novel complete protein coding human cDNAs.";
RL   Genome Res. 11:422-435(2001).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Spleen;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Testis;
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1-175.
RX   PubMed=15498874; DOI=10.1073/pnas.0404089101;
RA   Wan D., Gong Y., Qin W., Zhang P., Li J., Wei L., Zhou X., Li H., Qiu X.,
RA   Zhong F., He L., Yu J., Yao G., Jiang H., Qian L., Yu Y., Shu H., Chen X.,
RA   Xu H., Guo M., Pan Z., Chen Y., Ge C., Yang S., Gu J.;
RT   "Large-scale cDNA transfection screening for genes related to cancer
RT   development and progression.";
RL   Proc. Natl. Acad. Sci. U.S.A. 101:15724-15729(2004).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 644-1050.
RC   TISSUE=Testis;
RX   PubMed=17974005; DOI=10.1186/1471-2164-8-399;
RA   Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U.,
RA   Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D.,
RA   Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A.,
RA   Wiemann S., Schupp I.;
RT   "The full-ORF clone resource of the German cDNA consortium.";
RL   BMC Genomics 8:399-399(2007).
RN   [6]
RP   FUNCTION, INTERACTION WITH RAB21 AND RAB5A, AND SUBCELLULAR LOCATION.
RX   PubMed=16525121; DOI=10.1242/jcs.02810;
RA   Zhang X., He X., Fu X.-Y., Chang Z.;
RT   "Varp is a Rab21 guanine nucleotide exchange factor and regulates endosome
RT   dynamics.";
RL   J. Cell Sci. 119:1053-1062(2006).
RN   [7]
RP   FUNCTION, AND INTERACTION WITH RAB38 AND RAB21.
RX   PubMed=18477474; DOI=10.1016/j.bbrc.2008.05.017;
RA   Wang F., Zhang H., Zhang X., Wang Y., Ren F., Zhang X., Zhai Y., Chang Z.;
RT   "Varp interacts with Rab38 and functions as its potential effector.";
RL   Biochem. Biophys. Res. Commun. 372:162-167(2008).
RN   [8]
RP   PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-1023, AND IDENTIFICATION BY
RP   MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   TISSUE=Cervix carcinoma;
RX   PubMed=18220336; DOI=10.1021/pr0705441;
RA   Cantin G.T., Yi W., Lu B., Park S.K., Xu T., Lee J.-D., Yates J.R. III;
RT   "Combining protein-based IMAC, peptide-based IMAC, and MudPIT for efficient
RT   phosphoproteomic analysis.";
RL   J. Proteome Res. 7:1346-1351(2008).
RN   [9]
RP   FUNCTION, INTERACTION WITH RAB21 AND VAMP7, AND SUBCELLULAR LOCATION.
RX   PubMed=19745841; DOI=10.1038/embor.2009.186;
RA   Burgo A., Sotirakis E., Simmler M.C., Verraes A., Chamot C., Simpson J.C.,
RA   Lanzetti L., Proux-Gillardeaux V., Galli T.;
RT   "Role of Varp, a Rab21 exchange factor and TI-VAMP/VAMP7 partner, in
RT   neurite growth.";
RL   EMBO Rep. 10:1117-1124(2009).
RN   [10]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   TISSUE=Leukemic T-cell;
RX   PubMed=19690332; DOI=10.1126/scisignal.2000007;
RA   Mayya V., Lundgren D.H., Hwang S.-I., Rezaul K., Wu L., Eng J.K.,
RA   Rodionov V., Han D.K.;
RT   "Quantitative phosphoproteomic analysis of T cell receptor signaling
RT   reveals system-wide modulation of protein-protein interactions.";
RL   Sci. Signal. 2:RA46-RA46(2009).
RN   [11]
RP   INTERACTION WITH RAB32.
RX   PubMed=21808068; DOI=10.1074/jbc.m111.261115;
RA   Nottingham R.M., Ganley I.G., Barr F.A., Lambright D.G., Pfeffer S.R.;
RT   "RUTBC1 protein, a Rab9A effector that activates GTP hydrolysis by Rab32
RT   and Rab33B proteins.";
RL   J. Biol. Chem. 286:33213-33222(2011).
RN   [12]
RP   FUNCTION, AND INTERACTION WITH KIF5A; KIF5C AND GOLGA4.
RX   PubMed=22705394; DOI=10.1016/j.devcel.2012.04.019;
RA   Burgo A., Proux-Gillardeaux V., Sotirakis E., Bun P., Casano A.,
RA   Verraes A., Liem R.K., Formstecher E., Coppey-Moisan M., Galli T.;
RT   "A molecular network for the transport of the TI-VAMP/VAMP7 vesicles from
RT   cell center to periphery.";
RL   Dev. Cell 23:166-180(2012).
RN   [13]
RP   PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-962; SER-970 AND THR-1023,
RP   AND IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   TISSUE=Erythroleukemia;
RX   PubMed=23186163; DOI=10.1021/pr300630k;
RA   Zhou H., Di Palma S., Preisinger C., Peng M., Polat A.N., Heck A.J.,
RA   Mohammed S.;
RT   "Toward a comprehensive characterization of a human cancer cell
RT   phosphoproteome.";
RL   J. Proteome Res. 12:260-271(2013).
RN   [14]
RP   X-RAY CRYSTALLOGRAPHY (2.0 ANGSTROMS) OF 659-921 IN COMPLEX WITH VAMP7,
RP   SUBUNIT, FUNCTION, SUBCELLULAR LOCATION, AND MUTAGENESIS OF ASP-679;
RP   ASP-681; MET-684 AND TYR-687.
RX   PubMed=23104059; DOI=10.1038/nsmb.2414;
RA   Schafer I.B., Hesketh G.G., Bright N.A., Gray S.R., Pryor P.R., Evans P.R.,
RA   Luzio J.P., Owen D.J.;
RT   "The binding of Varp to VAMP7 traps VAMP7 in a closed, fusogenically
RT   inactive conformation.";
RL   Nat. Struct. Mol. Biol. 19:1300-1309(2012).
RN   [15]
RP   X-RAY CRYSTALLOGRAPHY (2.8 ANGSTROMS) OF 450-640 IN COMPLEX WITH RAB32,
RP   FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH VPS29, AND MUTAGENESIS OF
RP   HIS-432; LEU-434; GLN-509; LEU-513; LYS-546; TYR-550; HIS-712 AND LEU-714.
RX   PubMed=24856514; DOI=10.1016/j.devcel.2014.04.010;
RA   Hesketh G.G., Perez-Dorado I., Jackson L.P., Wartosch L., Schafer I.B.,
RA   Gray S.R., McCoy A.J., Zeldin O.B., Garman E.F., Harbour M.E., Evans P.R.,
RA   Seaman M.N., Luzio J.P., Owen D.J.;
RT   "VARP is recruited on to endosomes by direct interaction with retromer,
RT   where together they function in export to the cell surface.";
RL   Dev. Cell 29:591-606(2014).
CC   -!- FUNCTION: May be a guanine exchange factor (GEF) for Rab21, Rab32 and
CC       Rab38 and regulate endosome dynamics (PubMed:16525121,
CC       PubMed:18477474). May regulate the participation of VAMP7 in membrane
CC       fusion events; in vitro inhibits VAMP7-mediated SNARE complex formation
CC       by trapping VAMP7 in a closed, fusogenically inactive conformation
CC       (PubMed:23104059). Involved in peripheral melanosomal distribution of
CC       TYRP1 in melanocytes; the function, which probably is implicating
CC       vesicle-trafficking, includes cooperation with Rab32, Rab38 and VAMP7
CC       (By similarity). Involved in the regulation of neurite growth; the
CC       function seems to require its GEF activity, probably towards Rab21, and
CC       VAMP7 but not Rab32/38 (By similarity). Proposed to be involved in
CC       Golgi sorting of VAMP7 and transport of VAMP7 vesicles to the cell
CC       surface; the function seems to implicate kinesin heavy chain isoform 5
CC       proteins, GOLGA4, RAB21 and MACF1 (PubMed:22705394). Required for the
CC       colocalization of VAMP7 and Rab21, probably on TGN sites
CC       (PubMed:19745841). Involved in GLUT1 endosome-to-plasma membrane
CC       trafficking; the function is dependent of association with VPS29
CC       (PubMed:24856514). Regulates the proper trafficking of melanogenic
CC       enzymes TYR, TYRP1 and DCT/TYRP2 to melanosomes in melanocytes (By
CC       similarity). {ECO:0000250|UniProtKB:Q3UMR0,
CC       ECO:0000269|PubMed:23104059, ECO:0000269|PubMed:24856514,
CC       ECO:0000305|PubMed:16525121, ECO:0000305|PubMed:18477474,
CC       ECO:0000305|PubMed:22705394}.
CC   -!- SUBUNIT: Interacts with RAB21 (GDP-bound form), VPS29, RAB32 (GTP-bound
CC       form), RAB38 (GTP-bound form), VAMP7, KIF5A, KIF5C, GOLGA4. Interacts
CC       with low affinity with RAB5. ANKRD27:RAB32 heterodimers can
CC       homodimerize to form tetramers. Can interact with RAB38 or RAB32, VPS29
CC       and VAMP7 simultaneously (PubMed:16525121, PubMed:18477474,
CC       PubMed:19745841, PubMed:22705394, PubMed:23104059, PubMed:24856514,
CC       PubMed:21808068). A decreased interaction with RAB32 seen in the
CC       presence of SGSM2 (PubMed:21808068). {ECO:0000269|PubMed:16525121,
CC       ECO:0000269|PubMed:18477474, ECO:0000269|PubMed:19745841,
CC       ECO:0000269|PubMed:21808068, ECO:0000269|PubMed:22705394,
CC       ECO:0000269|PubMed:23104059, ECO:0000269|PubMed:24856514}.
CC   -!- INTERACTION:
CC       Q96NW4; Q13439: GOLGA4; NbExp=2; IntAct=EBI-6125599, EBI-1037845;
CC       Q96NW4; Q12840: KIF5A; NbExp=4; IntAct=EBI-6125599, EBI-713468;
CC       Q96NW4; P33175: Kif5a; Xeno; NbExp=2; IntAct=EBI-6125599, EBI-349710;
CC       Q96NW4; P70280: Vamp7; Xeno; NbExp=13; IntAct=EBI-6125599, EBI-6555653;
CC       Q96NW4; Q9JHW5: Vamp7; Xeno; NbExp=4; IntAct=EBI-6125599, EBI-919936;
CC   -!- SUBCELLULAR LOCATION: Early endosome {ECO:0000269|PubMed:16525121,
CC       ECO:0000269|PubMed:24856514}. Late endosome
CC       {ECO:0000269|PubMed:23104059}. Cytoplasmic vesicle membrane
CC       {ECO:0000269|PubMed:23104059}. Lysosome {ECO:0000269|PubMed:23104059}.
CC       Cell membrane {ECO:0000269|PubMed:23104059}. Melanosome
CC       {ECO:0000250|UniProtKB:Q3UMR0}. Note=Colocalizes with VAMP7 in
CC       transport vesicles in the shaft of hippocampal neurons (By similarity).
CC       {ECO:0000250|UniProtKB:Q3UMR0}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=BAB70755.1; Type=Erroneous initiation; Evidence={ECO:0000305};
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DR   EMBL; AL136784; CAB66718.1; -; mRNA.
DR   EMBL; AK054561; BAB70755.1; ALT_INIT; mRNA.
DR   EMBL; BC050529; AAH50529.1; -; mRNA.
DR   EMBL; AF447882; AAQ04657.1; -; mRNA.
DR   EMBL; AL834335; CAD39003.1; -; mRNA.
DR   CCDS; CCDS32986.1; -.
DR   RefSeq; NP_115515.2; NM_032139.2.
DR   RefSeq; XP_006723475.1; XM_006723412.2.
DR   PDB; 4B93; X-ray; 2.00 A; B=659-921.
DR   PDB; 4CYM; X-ray; 2.80 A; D/E/F=450-640.
DR   PDB; 4CZ2; X-ray; 2.97 A; D/E/F=450-640.
DR   PDB; 6TL0; NMR; -; B=692-746.
DR   PDBsum; 4B93; -.
DR   PDBsum; 4CYM; -.
DR   PDBsum; 4CZ2; -.
DR   PDBsum; 6TL0; -.
DR   AlphaFoldDB; Q96NW4; -.
DR   SMR; Q96NW4; -.
DR   BioGRID; 123874; 30.
DR   DIP; DIP-57614N; -.
DR   IntAct; Q96NW4; 21.
DR   MINT; Q96NW4; -.
DR   STRING; 9606.ENSP00000304292; -.
DR   iPTMnet; Q96NW4; -.
DR   PhosphoSitePlus; Q96NW4; -.
DR   BioMuta; ANKRD27; -.
DR   DMDM; 125987706; -.
DR   CPTAC; CPTAC-1175; -.
DR   CPTAC; CPTAC-1198; -.
DR   EPD; Q96NW4; -.
DR   jPOST; Q96NW4; -.
DR   MassIVE; Q96NW4; -.
DR   MaxQB; Q96NW4; -.
DR   PaxDb; Q96NW4; -.
DR   PeptideAtlas; Q96NW4; -.
DR   PRIDE; Q96NW4; -.
DR   ProteomicsDB; 77566; -.
DR   Antibodypedia; 47942; 86 antibodies from 23 providers.
DR   DNASU; 84079; -.
DR   Ensembl; ENST00000306065.9; ENSP00000304292.3; ENSG00000105186.16.
DR   GeneID; 84079; -.
DR   KEGG; hsa:84079; -.
DR   MANE-Select; ENST00000306065.9; ENSP00000304292.3; NM_032139.3; NP_115515.2.
DR   UCSC; uc002ntn.2; human.
DR   CTD; 84079; -.
DR   DisGeNET; 84079; -.
DR   GeneCards; ANKRD27; -.
DR   HGNC; HGNC:25310; ANKRD27.
DR   HPA; ENSG00000105186; Low tissue specificity.
DR   MIM; 618957; gene.
DR   neXtProt; NX_Q96NW4; -.
DR   OpenTargets; ENSG00000105186; -.
DR   PharmGKB; PA134893411; -.
DR   VEuPathDB; HostDB:ENSG00000105186; -.
DR   eggNOG; KOG2319; Eukaryota.
DR   GeneTree; ENSGT00940000157021; -.
DR   HOGENOM; CLU_010760_0_1_1; -.
DR   InParanoid; Q96NW4; -.
DR   OMA; LCHPLCT; -.
DR   OrthoDB; 871322at2759; -.
DR   PhylomeDB; Q96NW4; -.
DR   TreeFam; TF351261; -.
DR   PathwayCommons; Q96NW4; -.
DR   Reactome; R-HSA-8876198; RAB GEFs exchange GTP for GDP on RABs.
DR   SignaLink; Q96NW4; -.
DR   BioGRID-ORCS; 84079; 9 hits in 1076 CRISPR screens.
DR   ChiTaRS; ANKRD27; human.
DR   GeneWiki; ANKRD27; -.
DR   GenomeRNAi; 84079; -.
DR   Pharos; Q96NW4; Tbio.
DR   PRO; PR:Q96NW4; -.
DR   Proteomes; UP000005640; Chromosome 19.
DR   RNAct; Q96NW4; protein.
DR   Bgee; ENSG00000105186; Expressed in choroid plexus epithelium and 200 other tissues.
DR   ExpressionAtlas; Q96NW4; baseline and differential.
DR   Genevisible; Q96NW4; HS.
DR   GO; GO:0030659; C:cytoplasmic vesicle membrane; IEA:UniProtKB-SubCell.
DR   GO; GO:0005829; C:cytosol; IDA:HPA.
DR   GO; GO:0005769; C:early endosome; IDA:UniProtKB.
DR   GO; GO:0043231; C:intracellular membrane-bounded organelle; IDA:HPA.
DR   GO; GO:0005770; C:late endosome; IDA:UniProtKB.
DR   GO; GO:0005764; C:lysosome; IDA:UniProtKB.
DR   GO; GO:0042470; C:melanosome; IEA:UniProtKB-SubCell.
DR   GO; GO:0016020; C:membrane; HDA:UniProtKB.
DR   GO; GO:0043005; C:neuron projection; IBA:GO_Central.
DR   GO; GO:0005886; C:plasma membrane; IDA:UniProtKB.
DR   GO; GO:0030133; C:transport vesicle; IBA:GO_Central.
DR   GO; GO:0097422; C:tubular endosome; IDA:UniProtKB.
DR   GO; GO:0005096; F:GTPase activator activity; IEA:UniProtKB-KW.
DR   GO; GO:0005085; F:guanyl-nucleotide exchange factor activity; IDA:MGI.
DR   GO; GO:0031267; F:small GTPase binding; IDA:UniProtKB.
DR   GO; GO:0000149; F:SNARE binding; IBA:GO_Central.
DR   GO; GO:0045022; P:early endosome to late endosome transport; IDA:MGI.
DR   GO; GO:0032456; P:endocytic recycling; IMP:UniProtKB.
DR   GO; GO:0035646; P:endosome to melanosome transport; IEA:Ensembl.
DR   GO; GO:0035544; P:negative regulation of SNARE complex assembly; IDA:UniProtKB.
DR   GO; GO:0048812; P:neuron projection morphogenesis; IBA:GO_Central.
DR   GO; GO:0050775; P:positive regulation of dendrite morphogenesis; IEA:Ensembl.
DR   GO; GO:0010976; P:positive regulation of neuron projection development; IEA:Ensembl.
DR   GO; GO:0015031; P:protein transport; IEA:UniProtKB-KW.
DR   Gene3D; 1.20.1050.80; -; 1.
DR   Gene3D; 1.25.40.20; -; 2.
DR   InterPro; IPR002110; Ankyrin_rpt.
DR   InterPro; IPR036770; Ankyrin_rpt-contain_sf.
DR   InterPro; IPR003123; VPS9.
DR   InterPro; IPR037191; VPS9_dom_sf.
DR   Pfam; PF00023; Ank; 2.
DR   Pfam; PF12796; Ank_2; 2.
DR   Pfam; PF02204; VPS9; 1.
DR   PRINTS; PR01415; ANKYRIN.
DR   SMART; SM00248; ANK; 8.
DR   SMART; SM00167; VPS9; 1.
DR   SUPFAM; SSF109993; SSF109993; 1.
DR   SUPFAM; SSF48403; SSF48403; 2.
DR   PROSITE; PS50297; ANK_REP_REGION; 1.
DR   PROSITE; PS50088; ANK_REPEAT; 8.
DR   PROSITE; PS51205; VPS9; 1.
PE   1: Evidence at protein level;
KW   3D-structure; ANK repeat; Cell membrane; Cytoplasmic vesicle; Endosome;
KW   GTPase activation; Guanine-nucleotide releasing factor; Lysosome; Membrane;
KW   Phosphoprotein; Protein transport; Reference proteome; Repeat; Transport.
FT   CHAIN           1..1050
FT                   /note="Ankyrin repeat domain-containing protein 27"
FT                   /id="PRO_0000274556"
FT   DOMAIN          233..371
FT                   /note="VPS9"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00550"
FT   REPEAT          396..426
FT                   /note="ANK 1"
FT   REPEAT          462..491
FT                   /note="ANK 2"
FT   REPEAT          495..524
FT                   /note="ANK 3"
FT   REPEAT          528..560
FT                   /note="ANK 4"
FT   REPEAT          564..593
FT                   /note="ANK 5"
FT   REPEAT          597..627
FT                   /note="ANK 6"
FT   REPEAT          668..698
FT                   /note="ANK 7"
FT   REPEAT          743..772
FT                   /note="ANK 8"
FT   REPEAT          776..805
FT                   /note="ANK 9"
FT   REPEAT          809..838
FT                   /note="ANK 10"
FT   REPEAT          842..871
FT                   /note="ANK 11"
FT   REGION          1..372
FT                   /note="Sufficient for GEF activity towards RAB21"
FT                   /evidence="ECO:0000269|PubMed:16525121"
FT   REGION          396..460
FT                   /note="Sufficient for interaction with VPS29"
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   REGION          451..730
FT                   /note="Interaction with RAB32"
FT                   /evidence="ECO:0000250|UniProtKB:Q3UMR0"
FT   REGION          451..600
FT                   /note="Interaction with RAB38"
FT                   /evidence="ECO:0000250|UniProtKB:Q3UMR0,
FT                   ECO:0000269|PubMed:18477474"
FT   REGION          625..665
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          658..707
FT                   /note="Required for interaction with VAMP7"
FT                   /evidence="ECO:0000250|UniProtKB:Q3UMR0,
FT                   ECO:0000269|PubMed:19745841, ECO:0000269|PubMed:23104059"
FT   REGION          692..746
FT                   /note="Sufficient for interaction with VPS29"
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   REGION          987..1050
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        626..658
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   MOD_RES         962
FT                   /note="Phosphoserine"
FT                   /evidence="ECO:0007744|PubMed:23186163"
FT   MOD_RES         970
FT                   /note="Phosphoserine"
FT                   /evidence="ECO:0007744|PubMed:23186163"
FT   MOD_RES         1023
FT                   /note="Phosphothreonine"
FT                   /evidence="ECO:0007744|PubMed:18220336,
FT                   ECO:0007744|PubMed:23186163"
FT   VARIANT         657
FT                   /note="S -> G (in dbSNP:rs2287669)"
FT                   /evidence="ECO:0000269|PubMed:11230166"
FT                   /id="VAR_030317"
FT   VARIANT         761
FT                   /note="P -> R (in dbSNP:rs2302970)"
FT                   /evidence="ECO:0000269|PubMed:11230166"
FT                   /id="VAR_030318"
FT   MUTAGEN         432
FT                   /note="H->A: Disrupts interaction with VPS29; when
FT                   associated with A-434."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         434
FT                   /note="L->A: Disrupts interaction with VPS29; when
FT                   associated with A-432."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         509
FT                   /note="Q->A: Disrupts interaction with RAB32."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         513
FT                   /note="L->D: Disrupts interaction with RAB32."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         546
FT                   /note="K->D: Impairs interaction with RAB32."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         550
FT                   /note="Y->A: Impairs interaction with RAB32."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         679
FT                   /note="D->A: Disrupts interaction with VAMP7."
FT                   /evidence="ECO:0000269|PubMed:23104059"
FT   MUTAGEN         681
FT                   /note="D->A: Disrupts interaction with VAMP7."
FT                   /evidence="ECO:0000269|PubMed:23104059"
FT   MUTAGEN         684
FT                   /note="M->D: Disrupts interaction with VAMP7."
FT                   /evidence="ECO:0000269|PubMed:23104059"
FT   MUTAGEN         687
FT                   /note="Y->S: Disrupts interaction with VAMP7."
FT                   /evidence="ECO:0000269|PubMed:23104059"
FT   MUTAGEN         712
FT                   /note="H->A: Disrupts interaction with VPS29; when
FT                   associated with A-714."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   MUTAGEN         714
FT                   /note="L->A: Disrupts interaction with VPS29; when
FT                   associated with A-712."
FT                   /evidence="ECO:0000269|PubMed:24856514"
FT   CONFLICT        160..175
FT                   /note="HRTFRECERKSLRHHI -> LIEHSENARERASVTT (in Ref. 4;
FT                   AAQ04657)"
FT                   /evidence="ECO:0000305"
FT   HELIX           466..473
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           476..484
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           499..506
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           509..517
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           532..538
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           542..551
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   STRAND          552..554
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           568..574
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           578..586
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           601..604
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           608..615
FT                   /evidence="ECO:0007829|PDB:4CYM"
FT   HELIX           668..678
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           682..689
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   STRAND          734..736
FT                   /evidence="ECO:0007829|PDB:6TL0"
FT   TURN            744..746
FT                   /evidence="ECO:0007829|PDB:6TL0"
FT   HELIX           747..753
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           759..765
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           780..787
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           790..798
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           813..819
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           823..825
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           826..831
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           846..852
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           856..864
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           880..882
FT                   /evidence="ECO:0007829|PDB:4B93"
FT   HELIX           888..892
FT                   /evidence="ECO:0007829|PDB:4B93"
SQ   SEQUENCE   1050 AA;  116984 MW;  C47A96AA15E420F9 CRC64;
     MALYDEDLLK NPFYLALQKC RPDLCSKVAQ IHGIVLVPCK GSLSSSIQST CQFESYILIP
     VEEHFQTLNG KDVFIQGNRI KLGAGFACLL SVPILFEETF YNEKEESFSI LCIAHPLEKR
     ESSEEPLAPS DPFSLKTIED VREFLGRHSE RFDRNIASFH RTFRECERKS LRHHIDSANA
     LYTKCLQQLL RDSHLKMLAK QEAQMNLMKQ AVEIYVHHEI YNLIFKYVGT MEASEDAAFN
     KITRSLQDLQ QKDIGVKPEF SFNIPRAKRE LAQLNKCTSP QQKLVCLRKV VQLITQSPSQ
     RVNLETMCAD DLLSVLLYLL VKTEIPNWMA NLSYIKNFRF SSLAKDELGY CLTSFEAAIE
     YIRQGSLSAK PPESEGFGDR LFLKQRMSLL SQMTSSPTDC LFKHIASGNQ KEVERLLSQE
     DHDKDTVQKM CHPLCFCDDC EKLVSGRLND PSVVTPFSRD DRGHTPLHVA AVCGQASLID
     LLVSKGAMVN ATDYHGATPL HLACQKGYQS VTLLLLHYKA SAEVQDNNGN TPLHLACTYG
     HEDCVKALVY YDVESCRLDI GNEKGDTPLH IAARWGYQGV IETLLQNGAS TEIQNRLKET
     PLKCALNSKI LSVMEAYHLS FERRQKSSEA PVQSPQRSVD SISQESSTSS FSSMSASSRQ
     EETKKDYREV EKLLRAVADG DLEMVRYLLE WTEEDLEDAE DTVSAADPEF CHPLCQCPKC
     APAQKRLAKV PASGLGVNVT SQDGSSPLHV AALHGRADLI PLLLKHGANA GARNADQAVP
     LHLACQQGHF QVVKCLLDSN AKPNKKDLSG NTPLIYACSG GHHELVALLL QHGASINASN
     NKGNTALHEA VIEKHVFVVE LLLLHGASVQ VLNKRQRTAV DCAEQNSKIM ELLQVVPSCV
     ASLDDVAETD RKEYVTVKIR KKWNSKLYDL PDEPFTRQFY FVHSAGQFKG KTSREIMARD
     RSVPNLTEGS LHEPGRQSVT LRQNNLPAQS GSHAAEKGNS DWPERPGLTQ TGPGHRRMLR
     RHTVEDAVVS QGPEAAGPLS TPQEVSASRS
 
 
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