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F1SF13_PIG | Cobl domain-containing protein. (406 aa) | ||||
CATIP | Uncharacterized protein. (398 aa) | ||||
LMOD2 | Leiomodin 2. (550 aa) | ||||
VIL1 | Villin-1; Epithelial cell-specific Ca(2+)-regulated actin-modifying protein that modulates the reorganization of microvillar actin filaments. Plays a role in the actin nucleation, actin filament bundle assembly, actin filament capping and severing. Binds phosphatidylinositol 4,5-bisphosphate (PIP2) and lysophosphatidic acid (LPA); binds LPA with higher affinity than PIP2. Binding to LPA increases its phosphorylation by SRC and inhibits all actin-modifying activities. Binding to PIP2 inhibits actin-capping and -severing activities but enhances actin-bundling activity. Regulates the inte [...] (826 aa) | ||||
DLG1 | Discs large MAGUK scaffold protein 1; Belongs to the MAGUK family. (939 aa) | ||||
ARPC4 | Actin related protein 2/3 complex subunit 4. (231 aa) | ||||
AIF1 | Allograft inflammatory factor 1; Actin-binding protein that enhances membrane ruffling and RAC activation. Enhances the actin-bundling activity of LCP1. Binds calcium. Plays a role in RAC signaling and in phagocytosis. May play a role in macrophage activation and function. Promotes the proliferation of vascular smooth muscle cells and of T-lymphocytes. Enhances lymphocyte migration. Plays a role in vascular inflammation (By similarity). Has a dual influence on glucose-induced insulin secretion: inhibition at low concentration and stimulation at high concentrations. (147 aa) | ||||
ARPC2 | 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. (273 aa) | ||||
MSRB1 | Methionine-R-sulfoxide reductase B1; Methionine-sulfoxide reductase that specifically reduces methionine (R)-sulfoxide back to methionine. While in many cases, methionine oxidation is the result of random oxidation following oxidative stress, methionine oxidation is also a post-translational modification that takes place on specific residue. Acts as a regulator of actin assembly by reducing methionine (R)-sulfoxide mediated by MICALs (MICAL1, MICAL2 or MICAL3) on actin, thereby promoting filament repolymerization. Plays a role in innate immunity by reducing oxidized actin, leading to a [...] (94 aa) | ||||
LOC100513346 | Coronin; Belongs to the WD repeat coronin family. (962 aa) | ||||
GSN | Gelsolin; Calcium-regulated, actin-modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. Plays a role in ciliogenesis (By similarity). Belongs to the villin/gelsolin family. (780 aa) | ||||
SPIRE1 | Spire type actin nucleation factor 1. (802 aa) | ||||
A0A287A9Q1_PIG | Uncharacterized protein. (136 aa) | ||||
GAS7 | Growth arrest specific 7. (519 aa) | ||||
WASHC3 | WASH complex subunit 3. (194 aa) | ||||
WAS | WASP actin nucleation promoting factor. (500 aa) | ||||
FHDC1 | FH2 domain containing 1. (1001 aa) | ||||
ATP5F1A | ATP synthase subunit alpha, 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 [...] (737 aa) | ||||
WASL | WASP like actin nucleation promoting factor. (511 aa) | ||||
DLG2 | Discs large MAGUK scaffold protein 2. (1012 aa) | ||||
PSTPIP1 | Proline-serine-threonine phosphatase interacting protein 1. (443 aa) | ||||
DIAPH1 | Diaphanous related formin 1. (817 aa) | ||||
CTTN | Cortactin. (685 aa) | ||||
HCLS1 | Hematopoietic cell-specific Lyn substrate 1. (525 aa) | ||||
SPIRE2 | Spire type actin nucleation factor 2. (763 aa) | ||||
WASHC5 | WASH complex subunit 5 isoform X1. (1159 aa) | ||||
MICALL2 | MICAL-like protein 2 isoform X1. (887 aa) | ||||
DIAPH3 | Diaphanous related formin 3. (1138 aa) | ||||
MSRB2 | Peptide-methionine (R)-S-oxide reductase; Methionine-sulfoxide reductase that specifically reduces methionine (R)-sulfoxide back to methionine. While in many cases methionine oxidation is the result of random oxidation following oxidative stress, methionine oxidation is also a post-translational modification that takes place on specific residues. (182 aa) | ||||
TTC17 | Tetratricopeptide repeat domain 17. (1141 aa) |