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Proteintech
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Immunogen sequence: LTQGYNNWT NGLYGYSWDM MVHSRSHQHV KITYRDGRTG ELGYLNPGVF TQSRRWKDHA DMLKQYATCL SRLLPKYNVT EPQIYFDIWV SINDRFQQRI FDPRVDIVQA AWSPFQRTSW VQPLLMDLSP WRAKLQEIKS SLDNHTEVVF IADFPGLHLE NFVSEDLGNT SIQLLQGEVT VELVAEQKNQ TLREGEKMQL PAGEYHKVYT TSPSPSCYMY VYVNTTELAL EQDLAYLQEL KEKVENGSET GPLPPELQPL LEGEVKGGPE PTPLVQTFLR RQQRLQEIER RRNTPFHERF FRFLLRKLYV FRRSFLMTCI SLRNLILGRP SLEQLAQEVT YANLRPFEAV GELNPSNTDS SHSNPPESNP DPVHSEF (383-758 aa encoded by BC013979 )
GGCX (gamma-glutamyl carboxylase), also known as GC or VKCFD1 (Vitamin K-dependent gamma-carboxylase), is a 758 amino acid multi-pass membrane protein. Localized to the membrane of the endoplasmic reticulum, GGCX functions to mediate the vitamin K-dependent carboxylation of glutamate residues on target proteins, thereby producing calcium binding gamma-carboxyglutamate (Gla) residues on these proteins and simultaneously converting vitamin K to vitamin K epoxide. GGCX exists as a monomer and, via its ability to modify glutamate residues, it accomplishes the post-translational changes that are necessary for the activity of all vitamin K-dependent proteins (such as blood coagulation and bone matrix proteins). Defects in the gene encoding GGCX are the cause of combined deficiency of vitamin K-dependent clotting factors 1 (VKCFD1) and PXE-like disorder with multiple coagulation factor deficiency, both of which are characterized by abnormal skin, blood or bone function.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: FLJ26629; Gamma-glutamyl carboxylase; Peptidyl-glutamate 4-carboxylase; Vitamin K gamma glutamyl carboxylase; Vitamin K-dependent gamma-carboxylase
基因别名: GC; GGCX; VKCFD1
UniProt ID: (Human) P38435, (Rat) O88496, (Mouse) Q9QYC7
Entrez Gene ID: (Human) 2677, (Rat) 81716, (Mouse) 56316