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A0A0M3QY84 | Rdx. (882 aa) | ||||
Dbus_chrXg787 | Pvf1; Belongs to the PDGF/VEGF growth factor family. (337 aa) | ||||
A0A0M5JBM8 | Ptp61F. (551 aa) | ||||
Dbus_chrXg1392 | Tao. (1011 aa) | ||||
A0A0M5JA71 | Ave. (117 aa) | ||||
A0A0M5J959 | CYLD. (550 aa) | ||||
Dbus_chr2Lg566 | Smt3. (135 aa) | ||||
Dbus_chrXg612 | Hep. (850 aa) | ||||
A0A0M5J706 | Serine/threonine-protein phosphatase. (303 aa) | ||||
Dbus_chr2Rg240 | Hppy. (1050 aa) | ||||
Dbus_chrXg1824 | Small ubiquitin-related modifier. (96 aa) | ||||
Dbus_chrXg880 | MKP-4. (386 aa) | ||||
A0A0M5J5A4 | Pk92B. (1341 aa) | ||||
Dbus_chr3Rg406 | InR. (2083 aa) | ||||
A0A0M5J458 | Aos. (448 aa) | ||||
Dbus_chr3Lg2 | Ptp61F. (426 aa) | ||||
A0A0M5J245 | Nf-YB. (150 aa) | ||||
A0A0M5J170 | RBR-type E3 ubiquitin transferase. (353 aa) | ||||
Dbus_chr3Lg352 | Ras85D. (184 aa) | ||||
Dbus_chr3Rg18 | Lkb1. (541 aa) | ||||
A0A0M5IZ97 | DopEcR. (339 aa) | ||||
A0A0M5IYQ0 | Aos. (446 aa) | ||||
A0A0M5IYI2 | Maker480. (394 aa) | ||||
A0A0M5IWD9 | XNP. (1907 aa) | ||||
Dbus_chrXg1831 | Non-specific serine/threonine protein kinase. (622 aa) | ||||
Dbus_chrXg1326 | Dual specificity protein phosphatase; Dual specificity phosphatase able to dephosphorylate phosphotyrosine, phosphoserine and phosphothreonine residues, with a preference for phosphotyrosine as a substrate. Belongs to the protein-tyrosine phosphatase family. Non- receptor class dual specificity subfamily. (226 aa) | ||||
Dbus_chrXg526 | Traf4. (144 aa) | ||||
Dbus_chrXg531 | Slpr. (1174 aa) | ||||
Dbus_chrXg138 | Rala. (201 aa) | ||||
A0A0M4F655 | XNP. (1344 aa) | ||||
A0A0M4F575 | Cno. (2600 aa) | ||||
Dbus_chr3Rg820 | ATP synthase subunit d, mitochondrial; Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the cent [...] (178 aa) | ||||
Dbus_chr3Rg500 | ALiX. (833 aa) | ||||
Dbus_chr3Rg387 | Spg; Belongs to the DOCK family. (1927 aa) | ||||
A0A0M4EZQ6 | Sac1. (603 aa) | ||||
Dbus_chr3Lg273 | Ubiquitin carboxyl-terminal hydrolase. (818 aa) | ||||
Dbus_chrXg436 | 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma; Mediates the production of the second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3). Plays an important role in the regulation of intracellular signaling cascades. (1229 aa) | ||||
A0A0M4EWK8 | Jeb. (558 aa) | ||||
Dbus_chrXg1691 | UbcD6; Belongs to the ubiquitin-conjugating enzyme family. (177 aa) | ||||
Dbus_chrXg1441 | Vav. (953 aa) | ||||
A0A0M4EVI6 | Lkb1. (541 aa) | ||||
Dbus_chrXg1078 | Serine/threonine-protein phosphatase. (303 aa) | ||||
Dbus_chrXg1066 | CG8184. (5172 aa) | ||||
A0A0M4EU56 | LIM domain-containing protein. (348 aa) | ||||
Dbus_chrXg820 | Phl. (435 aa) | ||||
Dbus_chr3Rg142 | UbcD6; Belongs to the ubiquitin-conjugating enzyme family. (151 aa) | ||||
A0A0M4ES49 | Step. (775 aa) | ||||
A0A0M4ERU5 | CG6108. (1343 aa) | ||||
A0A0M4ER09 | Crc. (337 aa) | ||||
A0A0M4ER08 | Ics. (282 aa) | ||||
A0A0M4EQV2 | CG5604. (2682 aa) | ||||
Dbus_chr2Lg742 | Cka. (749 aa) | ||||
Dbus_chr3Rg935 | Alph. (371 aa) | ||||
A0A0M4EPM2 | CG17917. (217 aa) | ||||
Dbus_chr2Lg672 | Mnn1. (703 aa) | ||||
A0A0M4ENY2 | PSR. (409 aa) | ||||
Dbus_chr3Rg372 | Puc; Belongs to the protein-tyrosine phosphatase family. Non- receptor class dual specificity subfamily. (458 aa) | ||||
A0A0M4ENM2 | Pebp1. (176 aa) | ||||
Dbus_chr2Lg55 | F-actin-capping protein subunit beta; F-actin-capping proteins bind in a Ca(2+)-independent manner to the fast growing ends of actin filaments (barbed end) thereby blocking the exchange of subunits at these ends. Unlike other capping proteins (such as gelsolin and severin), these proteins do not sever actin filaments. (276 aa) | ||||
Dbus_chr3Lg508 | Msn. (1163 aa) | ||||
A0A0M4EN75 | Non-specific serine/threonine protein kinase. (802 aa) | ||||
A0A0M4EMY2 | Dual specificity protein phosphatase; Belongs to the protein-tyrosine phosphatase family. Non- receptor class dual specificity subfamily. (454 aa) | ||||
A0A0M4EMC1 | Arr1. (476 aa) | ||||
Dbus_chrXg527 | Traf6. (470 aa) | ||||
Dbus_chrXg352 | RhoGAP5A. (485 aa) | ||||
Dbus_chrXg340 | Peb. (1632 aa) | ||||
Dbus_chr3Rg765 | CG5073. (210 aa) | ||||
A0A0M4EKP5 | Battenin. (423 aa) | ||||
Dbus_chrXg1772 | Sgg. (1216 aa) | ||||
A0A0M4EKB3 | Mbc; Belongs to the DOCK family. (1971 aa) | ||||
Dbus_chr3Rg227 | Mekk1. (1571 aa) | ||||
A0A0M4EK43 | Lnk. (715 aa) | ||||
Dbus_chrXg1422 | Cdc42. (191 aa) | ||||
A0A0M4EIS7 | Ksr. (1053 aa) | ||||
A0A0M4EIA0 | CG7530. (350 aa) | ||||
Dbus_chr3Lg604 | Cbl. (796 aa) | ||||
A0A0M4EGS3 | Pde8; Belongs to the cyclic nucleotide phosphodiesterase family. (343 aa) | ||||
A0A0M4EGE4 | CG11539. (204 aa) | ||||
A0A0M4EG25 | CG7054. (156 aa) | ||||
A0A0M4EFN5 | Tum. (628 aa) | ||||
A0A0M4EFG3 | Alk. (1422 aa) | ||||
A0A0M4EF83 | Cbl. (845 aa) | ||||
A0A0M4EEW8 | Egfr. (780 aa) | ||||
Dbus_chr2Lg827 | Traf4. (486 aa) | ||||
Dbus_chr2Lg602 | Rbbp5. (80 aa) | ||||
Dbus_chr3Rg691 | PEK. (1074 aa) | ||||
Dbus_chr2Rg630 | POSH. (820 aa) | ||||
Dbus_chr3Lg750 | Aplip1. (473 aa) | ||||
Dbus_chr3Lg112 | Mtl. (192 aa) | ||||
Dbus_chr2Rg669 | Cnk. (1589 aa) | ||||
Dbus_chr2Lg982 | Pvr. (1104 aa) | ||||
A0A0M4EAC7 | PTP-ER. (1324 aa) | ||||
A0A0M4EA95 | CG10176. (180 aa) | ||||
A0A0M4E5A9 | Autophagy-related protein 9; Involved in autophagy and cytoplasm to vacuole transport (Cvt) vesicle formation. Plays a key role in the organization of the preautophagosomal structure/phagophore assembly site (PAS), the nucleating site for formation of the sequestering vesicle. Belongs to the ATG9 family. (850 aa) | ||||
Dbus_chr2Rg420 | CG11107. (731 aa) | ||||
A0A0M4E138 | Raw. (783 aa) | ||||
Dbus_chr2Lg601 | Ebi. (707 aa) | ||||
Dbus_chr2Lg116 | Maker379. (226 aa) | ||||
Dbus_chrXg1615 | Rab3-GEF. (2086 aa) | ||||
Dbus_chrXg1015 | Traf-like. (475 aa) | ||||
Dbus_chrXg285 | MAPk-Ak2; Belongs to the protein kinase superfamily. (349 aa) | ||||
Dbus_chr4g7 | Crk. (303 aa) | ||||
A0A0M3QYN7 | Alg-2. (145 aa) | ||||
A0A0M3QY59 | RuvB-like helicase; Proposed core component of the chromatin remodeling Ino80 complex which is involved in transcriptional regulation, DNA replication and probably DNA repair. (456 aa) | ||||
A0A0M3QY01 | CG10298. (194 aa) | ||||
Dbus_chr3Rg673 | Non-specific serine/threonine protein kinase. (568 aa) | ||||
A0A0M3QX42 | sNPF-R; Belongs to the G-protein coupled receptor 1 family. (595 aa) | ||||
A0A0M3QX40 | CG14184. (113 aa) | ||||
A0A0M3QX04 | Rpr. (69 aa) | ||||
Dbus_chr3Lg905 | CG11526. (898 aa) | ||||
Dbus_chr3Lg425 | Th. (412 aa) | ||||
Dbus_chr3Lg259 | Uev1A. (145 aa) | ||||
A0A0M3QVN9 | Hpo. (670 aa) | ||||
A0A0M3QVI0 | CG17765. (170 aa) | ||||
A0A0M3QVH1 | Slim. (588 aa) | ||||
A0A0M3QV48 | Spred. (426 aa) | ||||
A0A0M3QV39 | CG42241. (771 aa) | ||||
A0A0M3QV23 | Drk. (187 aa) | ||||
A0A0M3QUY8 | Mos; Belongs to the protein kinase superfamily. (399 aa) | ||||
A0A0M3QUY7 | Protein Wnt; Ligand for members of the frizzled family of seven transmembrane receptors; Belongs to the Wnt family. (358 aa) | ||||
Dbus_chr2Rg78 | F-actin-capping protein subunit alpha; F-actin-capping proteins bind in a Ca(2+)-independent manner to the fast growing ends of actin filaments (barbed end) thereby blocking the exchange of subunits at these ends. Unlike other capping proteins (such as gelsolin and severin), these proteins do not sever actin filaments. (286 aa) | ||||
A0A0M3QU37 | CG6043. (956 aa) | ||||
A0A0M3QU08 | C-cup. (224 aa) | ||||
Dbus_chr2Lg814 | Poe. (5355 aa) | ||||
Dbus_chr2Lg148 | Ced-12. (725 aa) |