Target intelligence / Profile preview

Serine incorporator 3 (SERINC3)

Target
SERINC3
Molecular classification
Transporter, Multipass transmembrane protein, Lipid transporter, Other (restriction factor for retroviruses)
01

Overview

Serine incorporator 3 (SERINC3) is a multipass transmembrane protein and member of the SERINC family, which facilitates the incorporation of serine into membrane phospholipids and sphingolipids, and functions as a lipid transporter and membrane scramblase[1][3][5]. It is expressed in the plasma membrane, is involved in the innate immune response against viruses as a restriction factor (especially HIV-1, by inhibiting viral fusion and entry), and is part of core lipid metabolic processes[1][5]. SERINC3 has roles in tissue-specific gene regulation, is subject to extensive posttranslational modification, and exhibits sequence variation that can impact protein function and regulation[2]. Disease associations include hereditary neuropathies, Duane retraction syndrome, alterations in bone and metabolic biomarkers, and potential links to tumor biology[1][4][5]. No clinically approved drugs are known to specifically target SERINC3, but its antiviral properties are of growing research interest.

Other names
SERC3SERC3_HUMANQ13530SERINC family member 3
02

Mechanism of action

Restriction of viral infectivity (retroviruses) by impeding membrane fusion/viral entry, specifically for HIV-1 and other lentiviruses

03

Biological functions

Phospholipid scrambling (scramblase activity)L-serine transmembrane transportAntiviral innate immune responseCell membrane lipid composition regulationFacilitate synthesis of serine-derived lipids (phosphatidylserine, sphingolipids)Carbohydrate derivative metabolismCell differentiation
04

Disease associations

Viral restriction (notably HIV-1)Neurological disorders (Spastic paraplegia 50, Autosomal recessive; Duane Retraction Syndrome)Cardiometabolic (decreased bone mineral density, increased glycerol levels; potential role in diabetes and cardiovascular disease)Auditory dysfunction (abnormal auditory brainstem response)Cancer (differential expression in tumors)
05

Safety considerations

No direct therapeutic targeting or drugs known, but knockout or loss-of-function phenotypes suggest roles in metabolic, neurological, and auditory homeostasisVariants/mutations may alter regulatory function and protein stability, which could theoretically present challenges in therapeutic modulation
06

Biomarkers

Circulating glycerol levels (associated with diabetes risk and SERINC3 knockout)Bone mineral density/contentAuditory brainstem response abnormalities

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