Tag | Content |
---|---|
UniProt Accession | TNNT2_HUMAN; P45379; |
Entrez ID | 7139 |
GenBank Protein ID | NM_000364.3; NM_001001430.2; NM_001001431.2; NM_001001432.2; NM_001276345.1; NM_001276346.1; NM_001276347.1; XM_006711508.3; XM_011509938.2; XM_011509939.1; XM_011509940.2; XM_011509942.2; XM_011509943.2; XM_017002217.1; |
GenBank Nucleotide ID | NP_000355.2; NP_001001430.1; NP_001001431.1; NP_001001432.1; NP_001263274.1; NP_001263275.1; NP_001263276.1; XP_006711571.1; XP_011508240.1; XP_011508241.1; XP_011508242.1; XP_011508244.1; XP_011508245.1; XP_016857706.1; |
Protein Name | Troponin T, cardiac muscle (TnTc) (Cardiac muscle troponin T) (cTnT) |
Gene Name | TNNT2 |
Organism | Homo sapiens |
NCBI Taxa ID | 9606 |
Functional Description | Troponin T is the tropomyosin-binding subunit of troponin, the thin filament regulatory complex which confers calcium-sensitivity to striated muscle actomyosin ATPase activity. |
Sequence (Fasta) | MSDIEEVVEE YEEEEQEEAA VEEEEDWRED EDEQEEAAEE DAEAEAETEE TRAEEDEEEE 60 EAKEAEDGPM EESKPKPRSF MPNLVPPKIP DGERVDFDDI HRKRMEKDLN ELQALIEAHF 120 ENRKKEEEEL VSLKDRIERR RAERAEQQRI RNEREKERQN RLAEERARRE EEENRRKAED 180 EARKKKALSN MMHFGGYIQK QAQTERKSGK RQTEREKKKK ILAERRKVLA IDHLNEDQLR 240 EKAKELWQSI YNLEAEKFDL QEKFKQQKYE INVLRNRIND NQKVSKTRGK AKVTGRWK 299 |
|
Database | Annotation |
---|---|
CTD (Curated) (count: 20) (view all) | MESH:D054058
; Acute Coronary Syndrome MESH:D006332 ; Cardiomegaly MESH:D009202 ; Cardiomyopathies MESH:D002311 ; Cardiomyopathy, Dilated MESH:C563306 ; Cardiomyopathy, Dilated, 1D MESH:C566171 ; Cardiomyopathy, Familial Hypertrophic, 2 |
GWASdb (count: 8) (view all) | rs2275863; Alcoholism (heaviness of drinking); alcohol dependence
rs3729842; Type 2 diabetes; type 2 diabetes mellitus rs6427901; Amyotrophic lateral sclerosis (sporadic); amyotrophic lateral sclerosis rs868407; Coronary heart disease; coronary artery disease rs6663175; Triglycerides; coronary artery disease|lipid metabolism disorder|arteriosclerosis rs3020556; Cardiac Troponin-T levels; congestive heart failure|coronary artery disease |
PTM | Modification Sites |
---|---|
Phosphorylation (count: 9) (view all) | 189 ARKKKALSNMMHFGG dbPAF
197 NMMHFGGYIQKQAQT dbPAF 2 ******MSDIEEVVE dbPAF 204 YIQKQAQTERKSGKR dbPAF 208 QAQTERKSGKRQTER dbPAF 213 RKSGKRQTEREKKKK dbPAF |
Glycation (count: 2) | 185 AEDEARKKKALSNMM PLMD
186 EDEARKKKALSNMMH PLMD |
Network | Interaction | ||
---|---|---|---|
A | B | Source | |