FKRP encodes glycosyltransferase-like protein and is considered as a causative gene of limb-girdle muscular dystrophy. FKRP has homology to glycosyltransferase-like protein Fukutin (considered as a causative gene of Fukuyama congenital muscular dystrophy), and thus named as fukutin-related protein (FKRP). The gene-knockout mice exhibit glycan structure alteration of α−dystroglycan. FKRP synthesizes the Rbo5P structure (Rbo5P-Rbo5P-3GalNAcb1-3GlcNAcb1-4(phospho-6)Man-Ser/Thr), the second of the tandem repeats of ribitol 5-phosphate (Rbo5P) in the O-mannose glycan structure of α−dystroglycan. The substrate sugar nucleotide, cytidine diphosphate ribitol (CDP-Rbo) is synthesized by isoprenoid synthase domain-containing protein (ISPD), which is also known as a causative gene of muscular dystrophy.
Keyword:
Limb-Girdle muscular dystrophy
, glycosyltransferase
, ribitol 5-phosphate (Rbo5P)
, α−dystroglycan
Glycosyltransferase-like
GGDB Symbol |
FKRP
Alias
HGNC Symbol
|
: |
FKRP
|
clone name
|
: |
FLJ12576 MGC2991
|
related terminology
|
: |
LGMD2I MDC1C MDDGA5 MDDGB5 MDDGC5
|
allelic
|
: |
LGMD2I MDC1C MDDGA5 MDDGB5 MDDGC5
|
|
|
|
Designation | hFKRP |
Organism | Homo sapiens |
GeneID |
79147
|
HGNC |
FKRP
(17997)
|
mRNA |
NM_024301
|
map | 19q13.33 |
Protein |
NP_077277
|
EC# |
|
CAZy |
|
GlyCosmos Glycogenes |
FKRP
|
OMIM |
606596
|
Disease name |
Congenital muscular dystrophy type 1C
, LGMD2I
, Limb-girdle muscular dystrophy 2I
, MDC1C
|
GDGDB |
CON00381
CON00382
|
Human Protein Atlas |
ENSG00000181027
|
Neuromuscul. Disord. 2001-12-01 ;69(6):1198-209.
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.
Brockington M. et al.
PMID:11592034
Cell Rep 2001-12-01 ;10(25):2851-9.
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.
Brockington M. et al.
PMID:11741828
Cell Rep 2015-06-01 ;25(6):474-84.
Dystroglycanopathy muscles lacking functional glycosylation of alpha-dystroglycan retain regeneration capacity.
Awano H. et al.
PMID:25937147
Hum. Mol. Genet. 2015-07-01 ;185(7):2025-37.
Restoration of Functional Glycosylation of α-Dystroglycan in FKRP Mutant Mice Is Associated with Muscle Regeneration.
Awano H. et al.
PMID:25976249
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This page does not indicate all of the enzymatic reaction, and expression of "FKRP".