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| A0A2L2TY33 | Adenylyl cyclase-associated protein; Belongs to the CAP family. (565 aa) | ||||
| A0A2L2TVP0 | Zn(2)-C6 fungal-type domain-containing protein. (435 aa) | ||||
| A0A2L2TV95 | Actin-related protein 2/3 complex subunit; Functions as component of the Arp2/3 complex which is involved in regulation of actin polymerization and together with an activating nucleation-promoting factor (NPF) mediates the formation of branched actin networks; Belongs to the WD repeat ARPC1 family. (363 aa) | ||||
| A0A2L2TUM4 | Zn(2)-C6 fungal-type domain-containing protein. (452 aa) | ||||
| A0A2L2TP07 | Zn(2)-C6 fungal-type domain-containing protein. (465 aa) | ||||
| A0A2L2TL05 | Uncharacterized protein; Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Myosin family. (1221 aa) | ||||
| A0A2L2TKJ1 | 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. (282 aa) | ||||
| A0A2L2TIN5 | Profilin; Binds to actin and affects the structure of the cytoskeleton. At high concentrations, profilin prevents the polymerization of actin, whereas it enhances it at low concentrations. (131 aa) | ||||
| A0A2L2TG86 | Uncharacterized protein. (618 aa) | ||||
| A0A2L2TDY0 | Uncharacterized protein. (332 aa) | ||||
| A0A2L2TDB4 | Uncharacterized protein. (1755 aa) | ||||
| A0A2L2TD69 | Uncharacterized protein. (143 aa) | ||||
| A0A2L2TAE4 | WD_REPEATS_REGION domain-containing protein. (610 aa) | ||||
| A0A2L2T9N8 | Uncharacterized protein. (332 aa) | ||||
| A0A2L2T9L3 | Uncharacterized protein. (265 aa) | ||||
| A0A2L2T9J0 | Zn(2)-C6 fungal-type domain-containing protein. (406 aa) | ||||
| A0A2L2T5H4 | Zn(2)-C6 fungal-type domain-containing protein. (434 aa) | ||||
| A0A2L2T3U7 | Actin-related protein 2/3 complex subunit 3; Functions as component of the Arp2/3 complex which is involved in regulation of actin polymerization and together with an activating nucleation-promoting factor (NPF) mediates the formation of branched actin networks. (192 aa) | ||||
| A0A2L2T3P7 | C2H2-type domain-containing protein. (629 aa) | ||||
| A0A2L2T331 | Uncharacterized protein. (832 aa) | ||||
| A0A2L2T1Z9 | Arp2/3 complex 34 kDa subunit; Functions as actin-binding component of the Arp2/3 complex which is involved in regulation of actin polymerization and together with an activating nucleation-promoting factor (NPF) mediates the formation of branched actin networks. (323 aa) | ||||
| A0A2L2T1P7 | Actin-related protein 2/3 complex subunit 5; Functions as component of the Arp2/3 complex which is involved in regulation of actin polymerization and together with an activating nucleation-promoting factor (NPF) mediates the formation of branched actin networks. Arp2/3 complex plays a critical role in the control of cell morphogenesis via the modulation of cell polarity development. (202 aa) | ||||
| A0A2L2T0U0 | DUF4045 domain-containing protein. (1558 aa) | ||||
| A0A2L2SW74 | Uncharacterized protein. (396 aa) | ||||
| A0A2L2SW04 | 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. (273 aa) | ||||
| A0A2L2SUL0 | Actin-related protein 2/3 complex subunit 4; Functions as actin-binding component of the Arp2/3 complex which is involved in regulation of actin polymerization and together with an activating nucleation-promoting factor (NPF) mediates the formation of branched actin networks. Seems to contact the mother actin filament; Belongs to the ARPC4 family. (169 aa) | ||||
| A0A2L2SUK8 | Uncharacterized protein. (656 aa) | ||||
| A0A2L2SSY6 | ADF-H domain-containing protein. (146 aa) | ||||
| A0A2L2SND3 | Uncharacterized protein. (1200 aa) | ||||