AlphaFold predicted structure
ABCA4 · P78363

Mean pLDDT
75.7/ 100
Confident
2,273 residues
Confidence breakdown
- Very high(≥ 90)10%
- Confident(70–90)67%
- Low(50–70)15%
- Very low(< 50)8%
AlphaFold (Jumper et al., 2021) · CC BY 4.0
ATP binding cassette subfamily A member 4
Annotations refreshed 1 month ago.
Diagnostic Grade (Green)
Retinal disorders
BIALLELIC, autosomal or pseudoautosomalGlaucoma (developmental)
Structural eye disease
BOTH monoallelic and biallelic, autosomal or pseudoautosomalsevere early-childhood-onset retinal dystrophy
Stargardt disease
cone-rod dystrophy 3
retinitis pigmentosa 19
age-related macular degeneration
retinitis pigmentosa
Cone rod dystrophy
cone-rod dystrophy
ABCA4-related retinopathy
age related macular degeneration 2
Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.
Retinal-specific phospholipid-transporting ATPase ABCA4
Flippase that catalyzes in an ATP-dependent manner the transport of retinal-phosphatidylethanolamine conjugates like 11-cis and all-trans isomers of N-retinylidene-phosphatidylethanolamine (N-Ret-PE) from the lumen to the cytoplasmic leaflet of photoreceptor outer segment disk membranes, where 11-cis-retinylidene-phosphatidylethanolamine is then isomerized to its all-trans isomer and reduced by RDH8 to produce all-trans-retinol. This transport activity ensures that all-trans-retinal generated from photoexcitation and 11-cis-retinal not needed for the regeneration of rhodopsin and cone opsins are effectively cleared from the photoreceptors, therefore preventing their accumulation and the formation of toxic bisretinoid (PubMed:10075733, PubMed:20404325, PubMed:22735453, PubMed:23144455, PubMed:24097981, PubMed:29847635, PubMed:33375396). Displays ATPase activity in vitro in absence of retinal substrate (PubMed:33605212, PubMed:39128720, PubMed:29847635, PubMed:33375396). May display GTPase activity that is strongly influenced by the lipid environment and the presence of retinoid compounds (PubMed:22735453). Binds the unprotonated form of N-retinylidene-phosphatidylethanolamine with high affinity in the absence of ATP, and ATP binding and hydrolysis induce a protein conformational change that causes N-retinylidene-phosphatidylethanolamine release (By similarity)
Curated MONDO disease pages that list ABCA4 among their top associated genes.
ABCA4 · P78363

Mean pLDDT
75.7/ 100
Confident
2,273 residues
Confidence breakdown
AlphaFold (Jumper et al., 2021) · CC BY 4.0