Features Interactions Isoform Disease Linear motifs Fingerprint Network All partners

ACTN4_HUMAN

F-actin cross-linking protein which is thought to anchor actin to a variety of intracellular structures. This is a bundling protein (Probable). Probably involved in vesicular trafficking via its association with the CART complex. The CART complex is necessary for efficient transferrin receptor recycling but not for EGFR degradation (PubMed). Involved in tight junction assembly in epithelial cells probably through interaction with MICALL2. Links MICALL2 to the actin cytoskeleton and recruits it to the tight junctions . May also function as a transcriptional coactivator, stimulating transcription mediated by the nuclear hormone receptors PPARG and RARA (PubMed). [View more on UniProt]

0100200300400500600700800900
Transmembrane
Phase separation
ELM
Phosphorylation
PFAM
Coiled coil
Anchor
Disordered
Interacting regions
Sequence
LOADING 64%

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0100200300400500600700800900
ACTN4_HUMAN
LOADING 67%
01002003004005006007008009001,0001,100
ACTN4_HUMAN
LOADING 67%

ACTN4_HUMAN has binary interactions with 50 proteins

ACTN4_HUMAN1433G_HUMANPP1B_HUMANSTAT1_HUMANHS71B_HUMANACTN4_HUMANHS71A_HUMANKCC2A_HUMANMYO5C_HUMANLRRC7_HUMANMARE1_HUMANDREB_HUMANSRC8_HUMANHGS_HUMANSYNPO_HUMANCAZA2_HUMANIMA1_HUMANDAPK1_HUMANACTN1_HUMANIQGA1_HUMANODPA_HUMANHSPB1_HUMANDLDH_HUMANCTNB1_HUMANMY18A_HUMANZO1_HUMANLIMA1_HUMANCTBP1_HUMANLNX1_HUMANTFR1_HUMANHSP7C_HUMANMYH9_HUMANSRC_HUMANKCC2B_HUMANPDLI7_HUMANSACS_HUMANDNM1L_HUMANKPCZ_HUMANMYO1C_HUMANACTN3_HUMANVINC_HUMANRS27_HUMANCAPZB_HUMANPRKN_HUMANACTB_HUMANFLNA_HUMANTRIM3_HUMANRAB13_HUMANCADH1_HUMANPRIO_HUMANTPM1_HUMANACTN4_HUMAN1433G_HUMANPP1B_HUMANSTAT1_HUMANHS71B_HUMANACTN4_HUMANHS71A_HUMANKCC2A_HUMANMYO5C_HUMANLRRC7_HUMANMARE1_HUMANDREB_HUMANSRC8_HUMANHGS_HUMANSYNPO_HUMANCAZA2_HUMANIMA1_HUMANDAPK1_HUMANACTN1_HUMANIQGA1_HUMANODPA_HUMANHSPB1_HUMANDLDH_HUMANCTNB1_HUMANMY18A_HUMANZO1_HUMANLIMA1_HUMANCTBP1_HUMANLNX1_HUMANTFR1_HUMANHSP7C_HUMANMYH9_HUMANSRC_HUMANKCC2B_HUMANPDLI7_HUMANSACS_HUMANDNM1L_HUMANKPCZ_HUMANMYO1C_HUMANACTN3_HUMANVINC_HUMANRS27_HUMANCAPZB_HUMANPRKN_HUMANACTB_HUMANFLNA_HUMANTRIM3_HUMANRAB13_HUMANCADH1_HUMANPRIO_HUMANTPM1_HUMAN
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0100200300400500600700800900
Interacting regions
Canonical [ACTN4_HUMAN]
Isoform [H7C144] alignment
Isoform [A0A8V8TL71] alignment
Isoform [K7EP19] alignment
Isoform [O43707-2] alignment
Isoform [O43707-3] alignment
Isoform [F5GXS2] alignment
LOADING 47%
Position Amino acid Mutation Disease Overlap with binding region
255 Lys Glu Focalsegmentalglomerulosclerosis1(FSGS1) -
259 Thr Ile Focalsegmentalglomerulosclerosis1(FSGS1) -
262 Ser Pro Focalsegmentalglomerulosclerosis1(FSGS1) -
262 Ser Phe Focalsegmentalglomerulosclerosis1(FSGS1) -
427 Ala Thr Focalsegmentalglomerulosclerosis1(FSGS1) -
748 Asn Asp Focalsegmentalglomerulosclerosis1(FSGS1) -
59 Trp Arg Focalsegmentalglomerulosclerosis1(FSGS1) -
72 Glu Gln Focalsegmentalglomerulosclerosis1(FSGS1) -

No annotated instance was found. To search for linear motifs, use the ELM prediction server.

Molecular function

Biological process

Disease

No data found.

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