
Rhodopsin
视紫质
Homo sapiensTaxon: 9606
348
氨基酸
38.9 kDa
理论值
4
PDB 条目
2
已记录
功能描述
定位与分布
组织特异性
Rod shaped photoreceptor cells which mediate vision in dim light
相关疾病
Retinitis pigmentosa 4
A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
Night blindness, congenital stationary, autosomal dominant 1
A non-progressive retinal disorder characterized by impaired night vision, often associated with nystagmus and myopia.
氨基酸序列
MNGTEGPNFYVPFSNATGVVRSPFEYPQYYLAEPWQFSMLAAYMFLLIVLGFPINFLTLY VTVQHKKLRTPLNYILLNLAVADLFMVLGGFTSTLYTSLHGYFVFGPTGCNLEGFFATLG GEIALWSLVVLAIERYVVVCKPMSNFRFGENHAIMGVAFTWVMALACAAPPLAGWSRYIP EGLQCSCGIDYYTLKPEVNNESFVIYMFVVHFTIPMIIIFFCYGQLVFTVKEAAAQQQES
FASTA 格式 · 348 个氨基酸 · 分子量 38.9 kDa
实验结构
4 PDB 条目翻译后修饰
- •Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region (By similarity). After activation by light, phosphorylated by GRK1 (in vitro) (PubMed:28524165)
- •Contains one covalently linked retinal chromophore. Upon light absorption, the covalently bound 11-cis-retinal is converted to all-trans-retinal. After hydrolysis of the Schiff base and release of the covalently bound all-trans-retinal, active rhodopsin is regenerated by binding of a fresh molecule of 11-cis-retinal (PubMed:12566452)