P51667

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession MLRV_MOUSE; P51667;
Entrez ID 17906
GenBank Protein ID
GenBank Nucleotide ID
Protein Name Myosin regulatory light chain 2, ventricular/cardiac muscle isoform (MLC-2) (MLC-2v) (Myosin light chain 2, slow skeletal/ventricular muscle isoform) (MLC-2s/v)
Gene Name Myl2; Mylpc
Organism Mus musculus
NCBI Taxa ID 10090
Functional DescriptionContractile protein that plays a role in heart development and function (PubMed:10409661). Following phosphorylation, plays a role in cross-bridge cycling kinetics and cardiac muscle contraction by increasing myosin lever arm stiffness and promoting myosin head diffusion; as a consequence of the increase in maximum contraction force and calcium sensitivity of contraction force. These events altogether slow down myosin kinetics and prolong duty cycle resulting in accumulated myosins being cooperatively recruited to actin binding sites to sustain thin filament activation as a means to fine-tune myofilament calcium sensitivity to force (By similarity) (PubMed:22426213, PubMed:16908724, PubMed:10409661). During cardiogenesis plays an early role in cardiac contractility by promoting cardiac myofibril assembly (PubMed:9422794).
Sequence
(Fasta)
MAPKKAKKRI EGGSSNVFSM FEQTQIQEFK EAFTIMDQNR DGFIDKNDLR DTFAALGRVN 60
VKNEEIDEMI KEAPGPINFT VFLTMFGEKL KGADPEETIL NAFKVFDPEG KGSLKADYVR 120
EMLTTQAERF SKEEIDQMFA AFPPDVTGNL DYKNLVHIIT HGEEKD 167

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1Serine PhosphorylationDilated cardiomyopathyPS14/1522426213
[Reference]: Loss of Mlc2v Ser14/Ser15 phosphorylation in vivo predisposes mice to dilated cardiomyopathy, heart failure, and premature death
2Serine PhosphorylationHeart failurePS14/1522426213
[Reference]: Loss of Mlc2v Ser14/Ser15 phosphorylation in vivo predisposes mice to dilated cardiomyopathy, heart failure, and premature death

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 3)
MESH:C563865 ; Cardiomyopathy, Familial Hypertrophic, 10
MESH:D002312 ; Cardiomyopathy, Hypertrophic
MESH:D024741 ; Cardiomyopathy, Hypertrophic, Familial

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 8)
(view all)
113       FDPEGKGSLKADYVR     dbPAF
118       KGSLKADYVREMLTT     dbPAF
125       YVREMLTTQAERFSK     dbPAF
14        KKRIEGGSSNVFSMF     dbPAF
15        KRIEGGSSNVFSMFE     dbPAF
19        GGSSNVFSMFEQTQI     dbPAF
Ubiquitination
(count: 8)
(view all)
111       KVFDPEGKGSLKADY     PLMD
115       PEGKGSLKADYVREM     PLMD
132       TQAERFSKEEIDQMF     PLMD
165       IITHGEEKD******     PLMD
46        NRDGFIDKNDLRDTF     PLMD
62        ALGRVNVKNEEIDEM     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource