KEGG   Homo sapiens (human): 29895
Entry
29895             CDS       T01001                                 
Symbol
MYL11, DA1C, HUMMLC2B, MLC2B, MRLC2, MYLPF
Name
(RefSeq) myosin light chain 11
  KO
K12758  fast skeletal myosin light chain 2
Organism
hsa  Homo sapiens (human)
Pathway
hsa04510  Focal adhesion
hsa04520  Adherens junction
hsa04670  Leukocyte transendothelial migration
hsa04810  Regulation of actin cytoskeleton
hsa04814  Motor proteins
hsa04820  Cytoskeleton in muscle cells
hsa05131  Shigellosis
Network
nt06181  Salmonella
nt06182  Shigella
nt06539  Cytoskeleton in muscle cells
  Element
N01074  Shigella IpaA to ITGA/B-RhoGEF-RhoA signaling pathway
N01130  Salmonella SopB to RhoA signaling pathway
N01817  Myosin thick filament
Disease
H00811  Distal arthrogryposis
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04814 Motor proteins
    29895 (MYL11)
   04820 Cytoskeleton in muscle cells
    29895 (MYL11)
 09150 Organismal Systems
  09151 Immune system
   04670 Leukocyte transendothelial migration
    29895 (MYL11)
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05131 Shigellosis
    29895 (MYL11)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    29895 (MYL11)
   04147 Exosome [BR:hsa04147]
    29895 (MYL11)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Actin filaments / Microfilaments
   Actin-binding proteins
    Myosins
     29895 (MYL11)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of hepatic cells
   29895 (MYL11)
SSDB
Motif
Pfam: EF-hand_7 EF-hand_1 EF-hand_6 EF-hand_8 EF-hand_5 AIF-1
Other DBs
NCBI-GeneID: 29895
NCBI-ProteinID: NP_001311387
OMIM: 617378
HGNC: 29824
Ensembl: ENSG00000180209
Pharos: Q96A32(Tbio)
UniProt: Q96A32
LinkDB
Position
16:30370934..30377991
AA seq 169 aa
MAPKRAKRRTVEGGSSSVFSMFDQTQIQEFKEAFTVIDQNRDGIIDKEDLRDTFAAMGRL
NVKNEELDAMMKEASGPINFTVFLTMFGEKLKGADPEDVITGAFKVLDPEGKGTIKKKFL
EELLTTQCDRFSQEEIKNMWAAFPPDVGGNVDYKNICYVITHGDAKDQE
NT seq 510 nt   +upstreamnt  +downstreamnt
atggcacccaagagggccaagagaaggacagtagagggcggaagctccagcgtcttctcc
atgttcgaccagactcagatccaggagttcaaagaggccttcactgtgatcgaccagaac
cgtgatggtattatagacaaggaggaccttcgggacaccttcgcagccatgggccgcctc
aatgtgaagaatgaggagttggatgccatgatgaaggaagccagcggtcccatcaacttc
accgtcttcctgaccatgttcggggagaagctcaagggtgccgaccctgaggatgtgatc
accggagccttcaaggtcttggaccctgagggaaagggcaccatcaagaagaagttcctg
gaggagctgctgaccacgcagtgtgaccgcttctcccaggaggagatcaagaacatgtgg
gcggccttcccccccgacgtgggcggcaacgtcgactacaaaaacatctgctacgtcatc
acgcacggcgacgccaaggaccaggagtag

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