Keratin, type II cytoskeletal 1 structure
P04264
K2C1_HUMAN
KRT1

Keratin, type II cytoskeletal 1

角蛋白,II 型细胞骨架 1

Homo sapiensTaxon: 9606

3D-structureCell membraneCitrullinationCoiled coilCytoplasmDirect protein sequencingDisease variantIchthyosisIntermediate filamentKeratinMembraneMethylation+4
序列长度

644

氨基酸

分子量

66.0 kDa

理论值

实验结构

3

PDB 条目

相关疾病

6

已记录

功能描述

May regulate the activity of kinases such as PKC and SRC via binding to integrin beta-1 (ITB1) and the receptor of activated protein C kinase 1 (RACK1). In complex with C1QBP is a high affinity receptor for kininogen-1/HMWK
可能通过与整合素 beta-1 (ITB1) 和活化蛋白 C 激酶 1 (RACK1) 受体结合来调节 PKC 和 SRC 等激酶的活性。 与 C1QBP 复合是激肽原-1/HMWK 的高亲和力受体
您所阅读的中文介绍为AI翻译机制自动翻译,并未经过人工审核,如有错漏,请以英文原文为准!

定位与分布

组织特异性

The source of this protein is neonatal foreskin. The 67-kDa type II keratins are expressed in terminally differentiating epidermis

相关疾病

Epidermolytic hyperkeratosis 1

A skin disorder characterized by widespread blistering and an ichthyotic erythroderma at birth that persist into adulthood. Histologically there is a diffuse epidermolytic degeneration in the lower spinous layer of the epidermis. Within a few weeks from birth, erythroderma and blister formation diminish and hyperkeratoses develop. EHK1 inheritance is autosomal dominant or autosomal recessive.

Ichthyosis hystrix, Curth-Macklin type

A genodermatosis with severe verrucous hyperkeratosis. Affected individuals manifest congenital verrucous black scale on the scalp, neck, and limbs with truncal erythema, palmoplantar keratoderma and keratoses on the lips, ears, nipples and buttocks.

Keratoderma, palmoplantar, non-epidermolytic

A dermatological disorder characterized by well-demarcated hyperkeratosis is present over the palms and soles. A red band is frequently present at the periphery of the keratosis. It is usually non-transgredient, with a sharp demarcation of the lesions at the wrists.

Ichthyosis, annular epidermolytic, 2

A form of annular epidermolytic ichthyosis, an autosomal dominant skin disorder characterized by polycyclic, migratory erythematous and scaly plaques. AEI2 patients manifest erythema and blistering of skin at birth that improves without scarring, as well as palmoplantar keratoderma.

Keratoderma, palmoplantar, striate 3

A dermatological disorder characterized by thickening of the stratum corneum and epidermal layers on palms and soles. There is no involvement of non-palmoplantar skin, and both hair and nails are normal.

Palmoplantar keratoderma, epidermolytic, 2

A form of epidermolytic palmoplantar keratoderma, a dermatological disorder characterized by diffuse thickening of the epidermis on the entire surface of palms and soles sharply bordered with erythematous margins. Some patients may present knuckle pads, thick pads of skin appearing over the proximal phalangeal joints. EPPK2 is an autosomal dominant form in which hyperkeratosis is restricted to palms and soles and is apparent from birth or childhood.

氨基酸序列

MSRQFSSRSGYRSGGGFSSGSAGIINYQRRTTSSSTRRSGGGGGRFSSCGGGGGSFGAGG
GFGSRSLVNLGGSKSISISVARGGGRGSGFGGGYGGGGFGGGGFGGGGFGGGGIGGGGFG
GFGSGGGGFGGGGFGGGGYGGGYGPVCPPGGIQEVTINQSLLQPLNVEIDPEIQKVKSRE
REQIKSLNNQFASFIDKVRFLEQQNQVLQTKWELLQQVDTSTRTHNLEPYFESFINNLRR

FASTA 格式 · 644 个氨基酸 · 分子量 66.0 kDa