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A0A0M4EJ20 | Maker763. (283 aa) | ||||
Dbus_chrXg1130 | AP-3 complex subunit beta; Belongs to the adaptor complexes large subunit family. (1149 aa) | ||||
Dbus_chrXg380 | AP-3 complex subunit delta; Belongs to the adaptor complexes large subunit family. (1080 aa) | ||||
Dbus_chrXg117 | Cm; Belongs to the adaptor complexes medium subunit family. (415 aa) | ||||
Dbus_chr3Lg740 | St. (672 aa) | ||||
A0A0M4F3Y7 | Kar. (569 aa) | ||||
A0A0M4EWU4 | Or. (191 aa) | ||||
A0A0M4EWA4 | Cd. (814 aa) | ||||
Dbus_chrXg1391 | Car; Belongs to the STXBP/unc-18/SEC1 family. (612 aa) | ||||
Dbus_chr2Rg549 | HPS4. (879 aa) | ||||
v | Tryptophan 2,3-dioxygenase; Heme-dependent dioxygenase that catalyzes the oxidative cleavage of the L-tryptophan (L-Trp) pyrrole ring and converts L- tryptophan to N-formyl-L-kynurenine. Catalyzes the oxidative cleavage of the indole moiety. (395 aa) | ||||
Dbus_chrXg53 | W. (451 aa) | ||||
Dbus_chr3Rg392 | Hermansky-Pudlak syndrome 5 protein homolog; Has a role in the biogenesis of eye pigment granules. Eye pigment granules are specialized forms of late endosomes or lysosomes. Biogenesis of pigment granules in the eye requires molecular components required for protein delivery to lysosomes. (851 aa) | ||||
A0A0M4EJ42 | St. (672 aa) | ||||
A0A0M3QV28 | Bw. (664 aa) | ||||
Dbus_chrXg29 | Dor. (1156 aa) | ||||
A0A0M4E3I5 | Vacuolar protein sorting-associated protein 41 homolog; Plays a role in vesicle-mediated protein trafficking to lysosomal compartments including the endocytic membrane transport pathways; Belongs to the VPS41 family. (843 aa) | ||||
A0A0M4EJ88 | Ca. (1879 aa) | ||||
A0A0M4EGK7 | Ltd. (702 aa) |