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GH12488

 B4JJG8_DROGR            Unreviewed;      2768 AA.
B4JJG8;
23-SEP-2008, integrated into UniProtKB/TrEMBL.
23-SEP-2008, sequence version 1.
25-OCT-2017, entry version 78.
SubName: Full=GH12488 {ECO:0000313|EMBL:EDV99720.1};
Name=Dgri\GH12488 {ECO:0000313|EMBL:EDV99720.1};
ORFNames=Dgri_GH12488 {ECO:0000313|EMBL:EDV99720.1},
GH12488 {ECO:0000313|FlyBase:FBgn0119967};
Drosophila grimshawi (Fruit fly) (Idiomyia grimshawi).
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta;
Pterygota; Neoptera; Holometabola; Diptera; Brachycera; Muscomorpha;
Ephydroidea; Drosophilidae; Drosophila; Hawaiian Drosophila.
NCBI_TaxID=7222 {ECO:0000313|Proteomes:UP000001070};
[1] {ECO:0000313|EMBL:EDV99720.1, ECO:0000313|Proteomes:UP000001070}
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
STRAIN=Tucson 15287-2541.00 {ECO:0000313|Proteomes:UP000001070};
PubMed=17994087; DOI=10.1038/nature06341;
Drosophila 12 Genomes Consortium;
Clark A.G., Eisen M.B., Smith D.R., Bergman C.M., Oliver B.,
Markow T.A., Kaufman T.C., Kellis M., Gelbart W., Iyer V.N.,
Pollard D.A., Sackton T.B., Larracuente A.M., Singh N.D., Abad J.P.,
Abt D.N., Adryan B., Aguade M., Akashi H., Anderson W.W.,
Aquadro C.F., Ardell D.H., Arguello R., Artieri C.G., Barbash D.A.,
Barker D., Barsanti P., Batterham P., Batzoglou S., Begun D.,
Bhutkar A., Blanco E., Bosak S.A., Bradley R.K., Brand A.D.,
Brent M.R., Brooks A.N., Brown R.H., Butlin R.K., Caggese C.,
Calvi B.R., Bernardo de Carvalho A., Caspi A., Castrezana S.,
Celniker S.E., Chang J.L., Chapple C., Chatterji S., Chinwalla A.,
Civetta A., Clifton S.W., Comeron J.M., Costello J.C., Coyne J.A.,
Daub J., David R.G., Delcher A.L., Delehaunty K., Do C.B., Ebling H.,
Edwards K., Eickbush T., Evans J.D., Filipski A., Findeiss S.,
Freyhult E., Fulton L., Fulton R., Garcia A.C., Gardiner A.,
Garfield D.A., Garvin B.E., Gibson G., Gilbert D., Gnerre S.,
Godfrey J., Good R., Gotea V., Gravely B., Greenberg A.J.,
Griffiths-Jones S., Gross S., Guigo R., Gustafson E.A., Haerty W.,
Hahn M.W., Halligan D.L., Halpern A.L., Halter G.M., Han M.V.,
Heger A., Hillier L., Hinrichs A.S., Holmes I., Hoskins R.A.,
Hubisz M.J., Hultmark D., Huntley M.A., Jaffe D.B., Jagadeeshan S.,
Jeck W.R., Johnson J., Jones C.D., Jordan W.C., Karpen G.H.,
Kataoka E., Keightley P.D., Kheradpour P., Kirkness E.F.,
Koerich L.B., Kristiansen K., Kudrna D., Kulathinal R.J., Kumar S.,
Kwok R., Lander E., Langley C.H., Lapoint R., Lazzaro B.P., Lee S.J.,
Levesque L., Li R., Lin C.F., Lin M.F., Lindblad-Toh K., Llopart A.,
Long M., Low L., Lozovsky E., Lu J., Luo M., Machado C.A.,
Makalowski W., Marzo M., Matsuda M., Matzkin L., McAllister B.,
McBride C.S., McKernan B., McKernan K., Mendez-Lago M., Minx P.,
Mollenhauer M.U., Montooth K., Mount S.M., Mu X., Myers E., Negre B.,
Newfeld S., Nielsen R., Noor M.A., O'Grady P., Pachter L.,
Papaceit M., Parisi M.J., Parisi M., Parts L., Pedersen J.S.,
Pesole G., Phillippy A.M., Ponting C.P., Pop M., Porcelli D.,
Powell J.R., Prohaska S., Pruitt K., Puig M., Quesneville H.,
Ram K.R., Rand D., Rasmussen M.D., Reed L.K., Reenan R., Reily A.,
Remington K.A., Rieger T.T., Ritchie M.G., Robin C., Rogers Y.H.,
Rohde C., Rozas J., Rubenfield M.J., Ruiz A., Russo S., Salzberg S.L.,
Sanchez-Gracia A., Saranga D.J., Sato H., Schaeffer S.W., Schatz M.C.,
Schlenke T., Schwartz R., Segarra C., Singh R.S., Sirot L., Sirota M.,
Sisneros N.B., Smith C.D., Smith T.F., Spieth J., Stage D.E.,
Stark A., Stephan W., Strausberg R.L., Strempel S., Sturgill D.,
Sutton G., Sutton G.G., Tao W., Teichmann S., Tobari Y.N.,
Tomimura Y., Tsolas J.M., Valente V.L., Venter E., Venter J.C.,
Vicario S., Vieira F.G., Vilella A.J., Villasante A., Walenz B.,
Wang J., Wasserman M., Watts T., Wilson D., Wilson R.K., Wing R.A.,
Wolfner M.F., Wong A., Wong G.K., Wu C.I., Wu G., Yamamoto D.,
Yang H.P., Yang S.P., Yorke J.A., Yoshida K., Zdobnov E., Zhang P.,
Zhang Y., Zimin A.V., Baldwin J., Abdouelleil A., Abdulkadir J.,
Abebe A., Abera B., Abreu J., Acer S.C., Aftuck L., Alexander A.,
An P., Anderson E., Anderson S., Arachi H., Azer M., Bachantsang P.,
Barry A., Bayul T., Berlin A., Bessette D., Bloom T., Blye J.,
Boguslavskiy L., Bonnet C., Boukhgalter B., Bourzgui I., Brown A.,
Cahill P., Channer S., Cheshatsang Y., Chuda L., Citroen M.,
Collymore A., Cooke P., Costello M., D'Aco K., Daza R., De Haan G.,
DeGray S., DeMaso C., Dhargay N., Dooley K., Dooley E., Doricent M.,
Dorje P., Dorjee K., Dupes A., Elong R., Falk J., Farina A., Faro S.,
Ferguson D., Fisher S., Foley C.D., Franke A., Friedrich D.,
Gadbois L., Gearin G., Gearin C.R., Giannoukos G., Goode T.,
Graham J., Grandbois E., Grewal S., Gyaltsen K., Hafez N., Hagos B.,
Hall J., Henson C., Hollinger A., Honan T., Huard M.D., Hughes L.,
Hurhula B., Husby M.E., Kamat A., Kanga B., Kashin S., Khazanovich D.,
Kisner P., Lance K., Lara M., Lee W., Lennon N., Letendre F.,
LeVine R., Lipovsky A., Liu X., Liu J., Liu S., Lokyitsang T.,
Lokyitsang Y., Lubonja R., Lui A., MacDonald P., Magnisalis V.,
Maru K., Matthews C., McCusker W., McDonough S., Mehta T., Meldrim J.,
Meneus L., Mihai O., Mihalev A., Mihova T., Mittelman R., Mlenga V.,
Montmayeur A., Mulrain L., Navidi A., Naylor J., Negash T., Nguyen T.,
Nguyen N., Nicol R., Norbu C., Norbu N., Novod N., O'Neill B.,
Osman S., Markiewicz E., Oyono O.L., Patti C., Phunkhang P.,
Pierre F., Priest M., Raghuraman S., Rege F., Reyes R., Rise C.,
Rogov P., Ross K., Ryan E., Settipalli S., Shea T., Sherpa N., Shi L.,
Shih D., Sparrow T., Spaulding J., Stalker J., Stange-Thomann N.,
Stavropoulos S., Stone C., Strader C., Tesfaye S., Thomson T.,
Thoulutsang Y., Thoulutsang D., Topham K., Topping I., Tsamla T.,
Vassiliev H., Vo A., Wangchuk T., Wangdi T., Weiand M., Wilkinson J.,
Wilson A., Yadav S., Young G., Yu Q., Zembek L., Zhong D., Zimmer A.,
Zwirko Z., Jaffe D.B., Alvarez P., Brockman W., Butler J., Chin C.,
Gnerre S., Grabherr M., Kleber M., Mauceli E., MacCallum I.;
"Evolution of genes and genomes on the Drosophila phylogeny.";
Nature 450:203-218(2007).
-!- CAUTION: Lacks conserved residue(s) required for the propagation
of feature annotation. {ECO:0000256|PROSITE-ProRule:PRU00076}.
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EMBL; CH916370; EDV99720.1; -; Genomic_DNA.
RefSeq; XP_001991096.1; XM_001991060.1.
ProteinModelPortal; B4JJG8; -.
STRING; 7222.FBpp0146394; -.
EnsemblMetazoa; FBtr0147902; FBpp0146394; FBgn0119967.
GeneID; 6564692; -.
KEGG; dgr:Dgri_GH12488; -.
FlyBase; FBgn0119967; Dgri\GH12488.
eggNOG; KOG1217; Eukaryota.
eggNOG; COG0666; LUCA.
InParanoid; B4JJG8; -.
KO; K02599; -.
OMA; QYVNSYT; -.
OrthoDB; EOG091G01NU; -.
PhylomeDB; B4JJG8; -.
Proteomes; UP000001070; Unassembled WGS sequence.
GO; GO:0005912; C:adherens junction; IEA:EnsemblMetazoa.
GO; GO:0009986; C:cell surface; IEA:EnsemblMetazoa.
GO; GO:0030139; C:endocytic vesicle; IEA:EnsemblMetazoa.
GO; GO:0016021; C:integral component of membrane; IEA:InterPro.
GO; GO:0005770; C:late endosome; IEA:EnsemblMetazoa.
GO; GO:0005764; C:lysosome; IEA:EnsemblMetazoa.
GO; GO:0005634; C:nucleus; IEA:EnsemblMetazoa.
GO; GO:0043234; C:protein complex; IEA:EnsemblMetazoa.
GO; GO:0035003; C:subapical complex; IEA:EnsemblMetazoa.
GO; GO:0005509; F:calcium ion binding; IEA:InterPro.
GO; GO:0003682; F:chromatin binding; IEA:EnsemblMetazoa.
GO; GO:0007015; P:actin filament organization; IEA:EnsemblMetazoa.
GO; GO:0007298; P:border follicle cell migration; IEA:EnsemblMetazoa.
GO; GO:0043697; P:cell dedifferentiation; IEA:EnsemblMetazoa.
GO; GO:0008407; P:chaeta morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0042688; P:crystal cell differentiation; IEA:EnsemblMetazoa.
GO; GO:0002213; P:defense response to insect; IEA:EnsemblMetazoa.
GO; GO:0008340; P:determination of adult lifespan; IEA:EnsemblMetazoa.
GO; GO:0046843; P:dorsal appendage formation; IEA:EnsemblMetazoa.
GO; GO:0009950; P:dorsal/ventral axis specification; IEA:EnsemblMetazoa.
GO; GO:0035162; P:embryonic hemopoiesis; IEA:EnsemblMetazoa.
GO; GO:0061331; P:epithelial cell proliferation involved in Malpighian tubule morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0035153; P:epithelial cell type specification, open tracheal system; IEA:EnsemblMetazoa.
GO; GO:0035214; P:eye-antennal disc development; IEA:EnsemblMetazoa.
GO; GO:0036099; P:female germ-line stem cell population maintenance; IEA:EnsemblMetazoa.
GO; GO:0007440; P:foregut morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0060288; P:formation of a compartment boundary; IEA:EnsemblMetazoa.
GO; GO:0060250; P:germ-line stem-cell niche homeostasis; IEA:EnsemblMetazoa.
GO; GO:0007403; P:glial cell fate determination; IEA:EnsemblMetazoa.
GO; GO:0008347; P:glial cell migration; IEA:EnsemblMetazoa.
GO; GO:0035172; P:hemocyte proliferation; IEA:EnsemblMetazoa.
GO; GO:0007157; P:heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules; IEA:EnsemblMetazoa.
GO; GO:0016348; P:imaginal disc-derived leg joint morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0048803; P:imaginal disc-derived male genitalia morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0008587; P:imaginal disc-derived wing margin morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0007474; P:imaginal disc-derived wing vein specification; IEA:EnsemblMetazoa.
GO; GO:0036335; P:intestinal stem cell homeostasis; IEA:EnsemblMetazoa.
GO; GO:0035171; P:lamellocyte differentiation; IEA:EnsemblMetazoa.
GO; GO:0046331; P:lateral inhibition; IEA:EnsemblMetazoa.
GO; GO:0007616; P:long-term memory; IEA:EnsemblMetazoa.
GO; GO:0061382; P:Malpighian tubule tip cell differentiation; IEA:EnsemblMetazoa.
GO; GO:0007498; P:mesoderm development; IEA:EnsemblMetazoa.
GO; GO:0008045; P:motor neuron axon guidance; IEA:EnsemblMetazoa.
GO; GO:0007521; P:muscle cell fate determination; IEA:EnsemblMetazoa.
GO; GO:2000048; P:negative regulation of cell-cell adhesion mediated by cadherin; IEA:EnsemblMetazoa.
GO; GO:0045316; P:negative regulation of compound eye photoreceptor development; IEA:EnsemblMetazoa.
GO; GO:0010629; P:negative regulation of gene expression; IEA:EnsemblMetazoa.
GO; GO:0035204; P:negative regulation of lamellocyte differentiation; IEA:EnsemblMetazoa.
GO; GO:0014019; P:neuroblast development; IEA:EnsemblMetazoa.
GO; GO:0007400; P:neuroblast fate determination; IEA:EnsemblMetazoa.
GO; GO:0097150; P:neuronal stem cell population maintenance; IEA:EnsemblMetazoa.
GO; GO:0007219; P:Notch signaling pathway; IEA:InterPro.
GO; GO:0030720; P:oocyte localization involved in germarium-derived egg chamber formation; IEA:EnsemblMetazoa.
GO; GO:0030713; P:ovarian follicle cell stalk formation; IEA:EnsemblMetazoa.
GO; GO:0007422; P:peripheral nervous system development; IEA:EnsemblMetazoa.
GO; GO:0008284; P:positive regulation of cell proliferation; IEA:EnsemblMetazoa.
GO; GO:0042691; P:positive regulation of crystal cell differentiation; IEA:EnsemblMetazoa.
GO; GO:1900087; P:positive regulation of G1/S transition of mitotic cell cycle; IEA:EnsemblMetazoa.
GO; GO:0043525; P:positive regulation of neuron apoptotic process; IEA:EnsemblMetazoa.
GO; GO:0045747; P:positive regulation of Notch signaling pathway; IEA:EnsemblMetazoa.
GO; GO:0045944; P:positive regulation of transcription from RNA polymerase II promoter; IEA:EnsemblMetazoa.
GO; GO:0048052; P:R1/R6 cell differentiation; IEA:EnsemblMetazoa.
GO; GO:0045466; P:R7 cell differentiation; IEA:EnsemblMetazoa.
GO; GO:0042686; P:regulation of cardioblast cell fate specification; IEA:EnsemblMetazoa.
GO; GO:0051489; P:regulation of filopodium assembly; IEA:EnsemblMetazoa.
GO; GO:0010906; P:regulation of glucose metabolic process; IEA:EnsemblMetazoa.
GO; GO:0006110; P:regulation of glycolytic process; IEA:EnsemblMetazoa.
GO; GO:0040008; P:regulation of growth; IEA:EnsemblMetazoa.
GO; GO:1902692; P:regulation of neuroblast proliferation; IEA:EnsemblMetazoa.
GO; GO:0009608; P:response to symbiont; IEA:EnsemblMetazoa.
GO; GO:0016330; P:second mitotic wave involved in compound eye morphogenesis; IEA:EnsemblMetazoa.
GO; GO:0016360; P:sensory organ precursor cell fate determination; IEA:EnsemblMetazoa.
GO; GO:0007519; P:skeletal muscle tissue development; IEA:EnsemblMetazoa.
GO; GO:0048190; P:wing disc dorsal/ventral pattern formation; IEA:EnsemblMetazoa.
CDD; cd00204; ANK; 2.
Gene3D; 1.25.40.20; -; 3.
Gene3D; 2.130.10.10; -; 1.
InterPro; IPR002110; Ankyrin_rpt.
InterPro; IPR020683; Ankyrin_rpt-contain_dom.
InterPro; IPR036770; Ankyrin_rpt-contain_sf.
InterPro; IPR024600; DUF3454_notch.
InterPro; IPR001881; EGF-like_Ca-bd_dom.
InterPro; IPR013032; EGF-like_CS.
InterPro; IPR000742; EGF-like_dom.
InterPro; IPR000152; EGF-type_Asp/Asn_hydroxyl_site.
InterPro; IPR018097; EGF_Ca-bd_CS.
InterPro; IPR009030; Growth_fac_rcpt_.
InterPro; IPR008297; Notch.
InterPro; IPR000800; Notch_dom.
InterPro; IPR035993; Notch_dom_like.
InterPro; IPR010660; Notch_NOD_dom.
InterPro; IPR011656; Notch_NODP_dom.
InterPro; IPR015943; WD40/YVTN_repeat-like_dom.
Pfam; PF12796; Ank_2; 2.
Pfam; PF11936; DUF3454; 1.
Pfam; PF00008; EGF; 24.
Pfam; PF07645; EGF_CA; 4.
Pfam; PF12661; hEGF; 2.
Pfam; PF06816; NOD; 1.
Pfam; PF07684; NODP; 1.
Pfam; PF00066; Notch; 3.
PIRSF; PIRSF002279; Notch; 1.
PRINTS; PR01452; LNOTCHREPEAT.
SMART; SM00248; ANK; 7.
SMART; SM01334; DUF3454; 1.
SMART; SM00181; EGF; 36.
SMART; SM00179; EGF_CA; 34.
SMART; SM00004; NL; 3.
SMART; SM01338; NOD; 1.
SMART; SM01339; NODP; 1.
SUPFAM; SSF48403; SSF48403; 1.
SUPFAM; SSF57184; SSF57184; 6.
SUPFAM; SSF90193; SSF90193; 3.
PROSITE; PS50297; ANK_REP_REGION; 1.
PROSITE; PS50088; ANK_REPEAT; 5.
PROSITE; PS00010; ASX_HYDROXYL; 22.
PROSITE; PS00022; EGF_1; 33.
PROSITE; PS01186; EGF_2; 27.
PROSITE; PS50026; EGF_3; 36.
PROSITE; PS01187; EGF_CA; 10.
PROSITE; PS50258; LNR; 3.
4: Predicted;
ANK repeat {ECO:0000256|PROSITE-ProRule:PRU00023};
Calcium {ECO:0000256|PIRSR:PIRSR002279-1};
Coiled coil {ECO:0000256|SAM:Coils};
Complete proteome {ECO:0000313|Proteomes:UP000001070};
Disulfide bond {ECO:0000256|PIRSR:PIRSR002279-2, ECO:0000256|PROSITE-
ProRule:PRU00076, ECO:0000256|SAAS:SAAS00601599};
EGF-like domain {ECO:0000256|PROSITE-ProRule:PRU00076,
ECO:0000256|SAAS:SAAS00032677};
Metal-binding {ECO:0000256|PIRSR:PIRSR002279-1};
Reference proteome {ECO:0000313|Proteomes:UP000001070};
Repeat {ECO:0000256|SAAS:SAAS00594563};
Signal {ECO:0000256|SAM:SignalP}.
SIGNAL 1 41 {ECO:0000256|SAM:SignalP}.
CHAIN 42 2768 {ECO:0000256|SAM:SignalP}.
/FTId=PRO_5002812246.
DOMAIN 56 93 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 94 136 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 139 176 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 177 215 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 217 253 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 255 291 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 293 329 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 331 369 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 371 407 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 408 446 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 448 485 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 487 523 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 525 561 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 563 599 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 601 636 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 638 674 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 676 712 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 714 750 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 752 788 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 790 826 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 828 864 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 866 904 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 906 943 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 945 981 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 983 1019 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1021 1057 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1059 1095 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1097 1133 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1150 1180 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1182 1218 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1220 1256 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1258 1294 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1296 1334 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1336 1372 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1374 1410 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1413 1449 EGF-like. {ECO:0000259|PROSITE:PS50026}.
DOMAIN 1521 1560 LNR. {ECO:0000259|PROSITE:PS50258}.
DOMAIN 1561 1596 LNR. {ECO:0000259|PROSITE:PS50258}.
DOMAIN 1598 1638 LNR. {ECO:0000259|PROSITE:PS50258}.
DOMAIN 1952 2194 ANK_REP_REGION.
{ECO:0000259|PROSITE:PS50297}.
REPEAT 2008 2040 ANK. {ECO:0000256|PROSITE-
ProRule:PRU00023}.
REPEAT 2041 2066 ANK. {ECO:0000256|PROSITE-
ProRule:PRU00023}.
REPEAT 2075 2107 ANK. {ECO:0000256|PROSITE-
ProRule:PRU00023}.
REPEAT 2108 2140 ANK. {ECO:0000256|PROSITE-
ProRule:PRU00023}.
REPEAT 2141 2173 ANK. {ECO:0000256|PROSITE-
ProRule:PRU00023}.
COILED 2580 2633 {ECO:0000256|SAM:Coils}.
METAL 467 467 Calcium 1; via carbonyl oxygen.
{ECO:0000256|PIRSR:PIRSR002279-1}.
METAL 470 470 Calcium 1; via amide nitrogen.
{ECO:0000256|PIRSR:PIRSR002279-1}.
METAL 490 490 Calcium 2.
{ECO:0000256|PIRSR:PIRSR002279-1}.
METAL 504 504 Calcium 2.
{ECO:0000256|PIRSR:PIRSR002279-1}.
METAL 528 528 Calcium 3.
{ECO:0000256|PIRSR:PIRSR002279-1}.
METAL 542 542 Calcium 3.
{ECO:0000256|PIRSR:PIRSR002279-1}.
METAL 543 543 Calcium 3; via carbonyl oxygen.
{ECO:0000256|PIRSR:PIRSR002279-1}.
DISULFID 83 92 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 126 135 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 166 175 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 186 203 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 205 214 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 243 252 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 281 290 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 319 328 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 359 368 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 397 406 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 417 434 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 436 445 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 452 464 {ECO:0000256|PIRSR:PIRSR002279-2}.
DISULFID 458 473 {ECO:0000256|PIRSR:PIRSR002279-2}.
DISULFID 475 484 {ECO:0000256|PIRSR:PIRSR002279-2,
ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 491 502 {ECO:0000256|PIRSR:PIRSR002279-2}.
DISULFID 496 511 {ECO:0000256|PIRSR:PIRSR002279-2}.
DISULFID 513 522 {ECO:0000256|PIRSR:PIRSR002279-2,
ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 529 540 {ECO:0000256|PIRSR:PIRSR002279-2}.
DISULFID 534 549 {ECO:0000256|PIRSR:PIRSR002279-2}.
DISULFID 551 560 {ECO:0000256|PIRSR:PIRSR002279-2,
ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 589 598 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 605 615 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 626 635 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 664 673 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 702 711 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 740 749 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 778 787 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 816 825 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 854 863 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 875 892 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 894 903 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 933 942 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 971 980 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1009 1018 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1047 1056 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1085 1094 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1123 1132 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1170 1179 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1208 1217 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1246 1255 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1284 1293 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1305 1322 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1324 1333 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1362 1371 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1378 1388 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1400 1409 {ECO:0000256|PROSITE-ProRule:PRU00076}.
DISULFID 1439 1448 {ECO:0000256|PROSITE-ProRule:PRU00076}.
SEQUENCE 2768 AA; 295187 MW; E9FBD6FD6E068032 CRC64;
MQLQRSRRRC RAHTIWINEM LAGVALLLPL LALATFSSAH ATGKCKDWQK SSSSSLAISC
TTLGCKNGGT CITQTNGKSY CACDTRYVGD YCEHRNPCLT GHGRCQNGGT CQVAFRNGRP
GISCLCPLGF EESLCEIAVP NACDQARCFN GGTCQLKTLQ EYSCICANGY TGEHCQTQNL
CASSPCRNGG TCSAMAGSSS FSCNCPPGFT GHTCSEDVEE CQSNPCQYGG TCVNTHGSYQ
CMCPAGYTGK DCDTKYKPCS PSPCQNGGTC RANGLTYDCK CPRGFEGKNC DQNIDDCPGN
LCQNGGTCVD GINDYRCNCP PNFTGRYCDV DVDECALRPS VCQNGATCTN THGTYSCICV
NGWAGSDCSE NIDDCVQAAC FYGATCIDGV GSFYCRCTPG KTGLLCHLDD ACTSNPCHAD
AICDTSPING SYACSCATGY KGVDCSEDID ECDQGSPCEH NGICVNTPGS FMCNCSQGFT
GPRCETNINE CESHPCQNEG SCLDDPGTFR CVCMPGFTGT QCEIDIDECQ SSPCLNDGIC
HDKINGFKCS CALGFTDVRC QINIDDCQSQ PCRNNGICRD SVAGYSCECA PGYTGASCEI
NINDCDSSPC HRGKCIDGDN SFKCACDPGF TGYLCQKQIN ECESNPCQFG GHCVDRVGSY
LCHCLPGTSG KNCEINVNEC HSNPCNNGAS CIDGINSYSC SCVPGFTGQH CELNVDECAS
NPCANNGVCM DLVNGYKCEC PRGFYDARCL SDVDECASSP CVNDGRCEDG INEFICHCPP
GYAGKRCEQD IDECASNPCQ HGGSCFDKLN AFSCQCMPGY TGHKCETNID DCLSNPCANG
GTCIDKVNGY KCVCKVPYTG LNCESQLDPC ASNRCRNEAK CTPSHNFLDF SCTCKLGYTG
RYCDEDINEC AFSSPCRNGA SCVNVPGSYR CLCTKGYEGR DCAINTDDCA SFPCQNGGTC
LDGIGDYSCL CVDGFDGKHC ETDINECLSM PCQNGATCHQ YVNSYTCTCP LGFSGINCQT
NDEDCTESSC LNGGSCVDGI NGYNCSCLVD YSGANCQYKL NKCDSGPCSN GGTCHEQRDG
YTCHCPSGYT GKQCSDYVDW CAQSPCENGA SCSQLKHQFN CKCAAGWTGK LCDVQTISCQ
DAAQRKGLSV KQLCNNGTCK NHGNSHVCYC SQGYAGSYCQ QDIDECASQP CQNGGTCRDL
VGAYECSCRQ GFQGQNCELN IDDCAPNPCQ NGGTCHDLVQ RFSCSCPPGT LGILCELNHD
DCVPGACHNN GSCIDRVGGF ECSCPPGFVG ARCEGDINEC LSNPCSNAGT LDCVQLVNNY
HCNCRPGHMG RHCEHKVNFC AQSPCQNGGA CSTKQSGHHC VCADGYYGKN CEFSGQDCDS
NPCRAGNCII DDAGGYRCEC SRGTAGQHCE IDTLDECQPN PCLQGAACDN LLGDYDCLCP
SKWTGKRCEI YDASYAGWSG NSNGNGGINS NGILINGNNN NGNGNNNNGN GNNIGNGNNG
NNNNGAAGIY AADLEQQRAM CEKRGCPEKQ SNGVCDSECN TYACNFDGND CSLGINPWAN
CTAPECWRVF MDGQCNEDCN NAACLYDGRD CEQKLKRCAA IYDAYCQKHY GDGYCDYGCN
NAECSWDGLD CEKSEQSPQL AEGAMSVVML MDVRQFRAEQ AQFLREMSHV LRTTVRVKKD
ALGNDMIFSW KGASRMPDIQ DSEFGRKHKI LYTHRNGQTG IQIYLEIDNR KCTECFNRAT
EAAEFLAASA AKHTFANRYP IYSVRGVQSP GEGEGAESPA NVKYVITGIV LVLILFAFFG
MVLSTHRKRA HGVTWFPEGF RAPAAAVMSR RRRDPHGQEM RNLNKQVGLS QSQAHQLPGG
VGSVAGGGVG SHWSDDESDM PQPKRQRGDQ LSSQLVGGSV AGLTSVGYAS DHTMISEYEE
ADQRVWSQAH LDVADVRAIM TPPAHQDGNK HDVDARGPCG LTPLMIAAVR GGGLDSGEDI
ENNEDSTAQV ISDLLAQGAE LNATMDKTGE TSLHLAARYA RADAAKRLLD AGADANCQDN
TGRTPLHAAV AADAMGVFQI LLRNRATNLN ARMHDGTTPL ILAARLAIEG MVEDLITADA
DINAADNSGK TALHWAAAVN NTEAVNILLM HHANRDAQDD KDETPLFLAA REGSYEACKA
LLDNFANREI TDHMDRLPRD VASERLHHDI VRLLDEHVPR SPQMISMTPQ AMIGSPPPGQ
QPQLITQPTV IAAGGAAGKQ SSQAAKQKAA KKAKLIEGNS PDNGLDTPGG SLRRKASSKK
GNNNNNNSSS NSAASKKAGM NGMNAASQLL LTASSVAAAQ AAICTDLDSP PPPQQTAAAA
AAAAAAATQA GNNGNLVNLN LPSPYDTSSM YSNAMAAPPN NNNNNGAKQP PSYEDCIKNA
QSLQSLPANS LDMIKLENYG YSMGSPFQQE MLNGQAMGLS GGRSTNTLCG LGGGLMPNGG
HEQGLSPPYS NQSPPHSVQS SLALSPHAYL GSPSPAKSRP SLPTSPTHIQ AMRHATQQKQ
FGSNLNSLLG GGNGSMGPQS SPVSLGIISP TGSDMGIMLA PQSSNNAKSS AIMQTLSPQL
QQQQQQQQQQ QQQHQQQQQQ QQQQQQQQQQ QQQQQQQQQQ QQQQQQQQQQ QQQAIGGLEF
GSAGLDLNGF CGSPDSFHSG QMNPPSIQSS MSGSSPSTNM LSPSSQHNQA FYQYLTPPSQ
HSGGHTPQHL VQTLDSYPTP SPESPGHWSS SSPRSNSDWS EGVQSPAANN LYISGGHQAN
KGSEAIYI


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