TCDB is operated by the Saier Lab Bioinformatics Group
« See all members of the family


1.A.36.1.1
The intracellular chloride channel, CLIC-like, Clcc1 (Mid1-related chloride [anion] channel, MCLC), of 551 aas. Its loss results in endoplasmic reticular (ER) stress, misfolded protein accumulation, and neurodegeneration (Jia et al. 2015).

Accession Number:Q96S66
Protein Name:MCLC aka HMCLC-1 aka KIAA0761
Length:551
Molecular Weight:62023.00
Species:Homo sapiens (Human) [9606]
Number of TMSs:3
Location1 / Topology2 / Orientation3: Membrane1 / Multi-pass membrane protein2
Substrate chloride

Cross database links:

RefSeq: NP_001041675.1    NP_055942.1   
Entrez Gene ID: 23155   
Pfam: PF05934   
KEGG: hsa:23155   

Gene Ontology

GO:0005783 C:endoplasmic reticulum
GO:0005794 C:Golgi apparatus
GO:0016021 C:integral to membrane
GO:0005634 C:nucleus

References (9)

[1] “Identification of a novel chloride channel expressed in the endoplasmic reticulum, Golgi apparatus, and nucleus.”  Nagasawa M.et.al.   11279057
[2] “Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.”  Nagase T.et.al.   9872452
[3] “The DNA sequence and biological annotation of human chromosome 1.”  Gregory S.G.et.al.   16710414
[4] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).”  The MGC Project Teamet.al.   15489334
[5] “Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.”  Olsen J.V.et.al.   17081983
[6] “Improved titanium dioxide enrichment of phosphopeptides from HeLa cells and high confident phosphopeptide identification by cross-validation of MS/MS and MS/MS/MS spectra.”  Yu L.-R.et.al.   17924679
[7] “Kinase-selective enrichment enables quantitative phosphoproteomics of the kinome across the cell cycle.”  Daub H.et.al.   18691976
[8] “A quantitative atlas of mitotic phosphorylation.”  Dephoure N.et.al.   18669648
[9] “Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.”  Gauci S.et.al.   19413330

External Searches:

Analyze:

Predict TMSs (Predict number of transmembrane segments)
Window Size: Angle:  
FASTA formatted sequence
1:	MLCSLLLCEC LLLVAGYAHD DDWIDPTDML NYDAASGTMR KSQAKYGISG EKDVSPDLSC 
61:	ADEISECYHK LDSLTYKIDE CEKKKREDYE SQSNPVFRRY LNKILIEAGK LGLPDENKGD 
121:	MHYDAEIILK RETLLEIQKF LNGEDWKPGA LDDALSDILI NFKFHDFETW KWRFEDSFGV 
181:	DPYNVLMVLL CLLCIVVLVA TELWTYVRWY TQLRRVLIIS FLFSLGWNWM YLYKLAFAQH 
241:	QAEVAKMEPL NNVCAKKMDW TGSIWEWFRS SWTYKDDPCQ KYYELLLVNP IWLVPPTKAL 
301:	AVTFTTFVTE PLKHIGKGTG EFIKALMKEI PALLHLPVLI IMALAILSFC YGAGKSVHVL 
361:	RHIGGPESEP PQALRPRDRR RQEEIDYRPD GGAGDADFHY RGQMGPTEQG PYAKTYEGRR 
421:	EILRERDVDL RFQTGNKSPE VLRAFDVPDA EAREHPTVVP SHKSPVLDTK PKETGGILGE 
481:	GTPKESSTES SQSAKPVSGQ DTSGNTEGSP AAEKAQLKSE AAGSPDQGST YSPARGVAGP 
541:	RGQDPVSSPC G