Tag | Content |
---|---|
UniProt Accession | ACM3_HUMAN; P20309; |
Entrez ID | 1131 |
GenBank Protein ID | NM_000740.3; NM_001347716.1; XM_005273032.3; XM_011544041.2; XM_011544043.2; XM_011544044.2; XM_011544046.2; XM_011544047.2; XM_017000152.1; XM_017000153.1; XM_017000154.1; XM_017000155.1; XM_017000156.1; XM_017000157.1; XM_017000158.1; XM_017000159.1; XM_017000160.1; XM_017000161.1; XM_017000162.1; XM_017000163.1; |
GenBank Nucleotide ID | NP_000731.1; NP_001334645.1; XP_005273089.1; XP_011542343.1; XP_011542345.1; XP_011542346.1; XP_011542348.1; XP_011542349.1; XP_016855641.1; XP_016855642.1; XP_016855643.1; XP_016855644.1; XP_016855645.1; XP_016855646.1; XP_016855647.1; XP_016855648.1; XP_016855649.1; XP_016855650.1; XP_016855651.1; XP_016855652.1; |
Protein Name | Muscarinic acetylcholine receptor M3 |
Gene Name | CHRM3 |
Organism | Homo sapiens |
NCBI Taxa ID | 9606 |
Functional Description | The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Primary transducing effect is Pi turnover. |
Sequence (Fasta) | MTLHNNSTTS PLFPNISSSW IHSPSDAGLP PGTVTHFGSY NVSRAAGNFS SPDGTTDDPL 60 GGHTVWQVVF IAFLTGILAL VTIIGNILVI VSFKVNKQLK TVNNYFLLSL ACADLIIGVI 120 SMNLFTTYII MNRWALGNLA CDLWLAIDYV ASNASVMNLL VISFDRYFSI TRPLTYRAKR 180 TTKRAGVMIG LAWVISFVLW APAILFWQYF VGKRTVPPGE CFIQFLSEPT ITFGTAIAAF 240 YMPVTIMTIL YWRIYKETEK RTKELAGLQA SGTEAETENF VHPTGSSRSC SSYELQQQSM 300 KRSNRRKYGR CHFWFTTKSW KPSSEQMDQD HSSSDSWNNN DAAASLENSA SSDEEDIGSE 360 TRAIYSIVLK LPGHSTILNS TKLPSSDNLQ VPEEELGMVD LERKADKLQA QKSVDDGGSF 420 PKSFSKLPIQ LESAVDTAKT SDVNSSVGKS TATLPLSFKE ATLAKRFALK TRSQITKRKR 480 MSLVKEKKAA QTLSAILLAF IITWTPYNIM VLVNTFCDSC IPKTFWNLGY WLCYINSTVN 540 PVCYALCNKT FRTTFKMLLL CQCDKKKRRK QQYQQRQSVI FHKRAPEQAL 591 |
|
Database | Annotation |
---|---|
CTD (Curated) (count: 6) | MESH:D001201
; Ascites MESH:D056486 ; Chemical and Drug Induced Liver Injury MESH:D003456 ; Cryptorchidism MESH:D008103 ; Liver Cirrhosis MESH:D011535 ; Prune Belly Syndrome MESH:D001745 ; Urinary Bladder Diseases |
DisGeNet (Curated) (count: 43) (view all) | C0003466; Anus, Imperforate
C0003962; Ascites C0005586; Bipolar Disorder C0005686; Urinary Bladder Diseases C0009081; Congenital clubfoot C0009806; Constipation |
HGMD (count: 1) | CR067509; Diabetes, type 2, increased risk, assoc. ?; Regulatory
|
GWASdb (count: 14) (view all) | rs10754677; Sudden cardiac arrest; coronary artery disease
rs1867266; Smoking initiation; nicotine dependence rs7523711; Multiple complex diseases; Null rs6694025; Multiple complex diseases; Null rs7527723; Multiple complex diseases; Null rs645248; Multiple complex diseases; Null |
PTM | Modification Sites |
---|---|
Phosphorylation (count: 3) | 291 TGSSRSCSSYELQQQ dbPAF
365 GSETRAIYSIVLKLP dbPAF 366 SETRAIYSIVLKLPG dbPAF |
Ubiquitination (count: 4) | 412 ADKLQAQKSVDDGGS PLMD
426 SFPKSFSKLPIQLES PLMD 439 ESAVDTAKTSDVNSS PLMD 449 DVNSSVGKSTATLPL PLMD |
Network | Interaction | ||
---|---|---|---|
A | B | Source | |