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A0A443HVB1 | Guanine nucleotide binding protein alpha subunit. (353 aa) | ||||
A0A443HZJ3 | Dynein light chain; Acts as one of several non-catalytic accessory components of the cytoplasmic dynein complex that are thought to be involved in linking dynein to cargos and to adapter proteins that regulate dynein function. Cytoplasmic dynein acts as a motor for the intracellular retrograde motility of vesicles and organelles along microtubules. May play a role in changing or maintaining the spatial distribution of cytoskeletal structures. (94 aa) | ||||
A0A443I0A3 | Putative phosphatidylinositol transporter. (344 aa) | ||||
A0A443I0A6 | Peroxin/Ferlin domain-containing protein. (480 aa) | ||||
A0A443I0V1 | Putative bZIP transcription factor. (639 aa) | ||||
A0A443I3N1 | Pterin-4-alpha-carbinolamine dehydratase family protein. (166 aa) | ||||
A0A443I3B7 | Tubulin alpha chain; Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. (452 aa) | ||||
A0A443I1N4 | Dynein heavy chain. (4346 aa) | ||||
A0A443I148 | Putative ubiquitin conjugating enzyme. (333 aa) | ||||
A0A443I8J7 | Putative SNF2 family helicase/ATPase. (1844 aa) | ||||
A0A443I8C4 | Putative COP9 signalosome subunit 6. (415 aa) | ||||
A0A443I7Z8 | Uncharacterized protein. (277 aa) | ||||
A0A443I7J3 | Putative COP9 signalosome subunit 1. (486 aa) | ||||
A0A443I795 | Chitin synthase F. (1199 aa) | ||||
A0A443I773 | DNA mismatch repair protein; Component of the post-replicative DNA mismatch repair system (MMR). (1126 aa) | ||||
A0A443I6P3 | Phosphatidyl-N-methylethanolamine N-methyltransferase; Catalyzes the second two steps of the methylation pathway of phosphatidylcholine biosynthesis, the SAM-dependent methylation of phosphatidylmonomethylethanolamine (PMME) to phosphatidyldimethylethanolamine (PDME) and of PDME to phosphatidylcholine (PC). (201 aa) | ||||
A0A443I6E7 | PITH domain-containing protein. (224 aa) | ||||
A0A443I4S7 | Uncharacterized protein. (1774 aa) | ||||
A0A443I4F8 | Putative histone-lysine N-methyltransferase. (833 aa) | ||||
A0A443I4D0 | Phosphatidylinositol-4-phosphate 5-kinase its3. (876 aa) | ||||
A0A443I4A0 | Phospholipase. (1752 aa) | ||||
A0A443I495 | Putative COP9 signalosome subunit 2. (494 aa) | ||||
A0A443I110 | Phospholipase. (866 aa) | ||||
MAT1-1-1 | Mating-type protein MAT alpha 1. (365 aa) | ||||
A0A443HHJ8 | Putative two-component histidine kinase Fos-1. (720 aa) | ||||
A0A443HHP9 | COP9 signalosome complex subunit 3. (503 aa) | ||||
A0A443HIE3 | Eisosome component PIL1-domain-containing protein. (320 aa) | ||||
A0A443HIL3 | Actin-related protein 2; ATP-binding component of the Arp2/3 complex, a multiprotein complex that mediates actin polymerization upon stimulation by nucleation-promoting factor (NPF). The Arp2/3 complex mediates the formation of branched actin networks in the cytoplasm, providing the force for cell motility. Seems to contact the pointed end of the daughter actin filament. (388 aa) | ||||
A0A443HJ36 | Uncharacterized protein. (294 aa) | ||||
A0A443HJD6 | Cell-cycle nuclear protein. (831 aa) | ||||
A0A443HJS2 | RRM domain-containing protein. (399 aa) | ||||
A0A443HJS4 | Uncharacterized protein. (218 aa) | ||||
A0A443HJT7 | Uncharacterized protein. (251 aa) | ||||
A0A443HKX1 | Sexual development transcription factor SteA. (692 aa) | ||||
A0A443HLS5 | Trehalose-6-phosphate synthase. (511 aa) | ||||
A0A443HML1 | Cytochrome P450 monooxygenase; Belongs to the cytochrome P450 family. (515 aa) | ||||
A0A443HN83 | PCI domain-containing protein. (329 aa) | ||||
A0A443HQZ1 | Trehalose-6-phosphate synthase. (482 aa) | ||||
A0A443HR08 | Uncharacterized protein. (606 aa) | ||||
A0A443HS01 | Putative leucine zipper transcription factor. (1866 aa) | ||||
A0A443HS83 | Putative cullin binding protein CanA. (1337 aa) | ||||
A0A443HSW8 | 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. (266 aa) | ||||
A0A443HTB5 | Phospholipase. (841 aa) | ||||
A0A443HTZ7 | PIPK domain-containing protein. (350 aa) | ||||
A0A443HUH3 | Rtf2 RING-finger-domain-containing protein. (311 aa) | ||||
A0A443HV08 | TATA element modulatory factor 1 TATA binding-domain-containing protein. (863 aa) |