KEGG T01001: 4632

Homo sapiens (human): 4632

Entry

4632              CDS       T01001

Symbol

MYL1, CMYP14, MLC-1, MLC1, MLC1/3, MLC1F, MLC3F, MYOFTA

Name

(RefSeq) myosin light chain 1

K05738

myosin light chain 1

Organism

hsa Homo sapiens (human)

Pathway

hsa04814

Motor proteins

hsa04820

Cytoskeleton in muscle cells

Network

nt06539 Cytoskeleton in muscle cells

Element

N01817

Myosin thick filament

Disease

H01810

Congenital myopathy

Brite

KEGG Orthology (KO) [BR:hsa00001]
09140 Cellular Processes
  09142 Cell motility
   04814 Motor proteins
    4632 (MYL1)
   04820 Cytoskeleton in muscle cells
    4632 (MYL1)
09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    4632 (MYL1)
Cytoskeleton proteins [BR:hsa04812]
Eukaryotic cytoskeleton proteins
  Actin filaments / Microfilaments
   Actin-binding proteins
    Myosins
     4632 (MYL1)

SSDB

Motif

Pfam:

EF-hand_7 EF-hand_6 EF-hand_1 AIF-1 EF-hand_9 KfrA_N

Other DBs

NCBI-GeneID:

NCBI-ProteinID:

OMIM:

HGNC:

Ensembl:

UniProt:

LinkDB

Position

2:complement(210290150..210315174)

AA seq 194 aa
MAPKKDVKKPVAAAAAAPAPAPAPAPAPAPAKPKEEKIDLSAIKIEFSKEQQDEFKEAFL
LFDRTGDSKITLSQVGDVLRALGTNPTNAEVRKVLGNPSNEELNAKKIEFEQFLPMMQAI
SNNKDQATYEDFVEGLRVFDKEGNGTVMGAELRHVLATLGEKMKEEEVEALMAGQEDSNG
CINYEAFVKHIMSI

NT seq 585 nt +upstreamnt +downstreamnt
atggcaccaaagaaagacgtgaagaaacctgtggctgcggctgcggctgccccagccccg
gcaccggcacctgcacctgcccctgccccagccaaacccaaagaagaaaaaattgacctc
tctgccattaagatcgagttctctaaggaacagcaggatgaattcaaggaggcatttctc
ctgtttgacagaacaggtgattccaagatcaccttaagccaggtcggtgatgtccttcga
gctctgggcacaaatcccaccaatgcagaggtcaggaaagttctgggaaaccccagcaat
gaagagctgaatgccaagaaaattgagtttgaacaatttctgcctatgatgcaagccatt
tccaacaacaaggaccaggccacctatgaagactttgttgagggtctgcgtgtctttgac
aaggaaggcaatggcacagtcatgggtgctgaactccgccatgttctagccaccctgggt
gaaaagatgaaagaggaagaagtggaagccctgatggcaggtcaagaagactccaatggc
tgcatcaactacgaagcttttgtcaagcacatcatgtctatctga

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