UniProt ID | CLCN2_HUMAN | |
---|---|---|
UniProt AC | P51788 | |
Protein Name | Chloride channel protein 2 | |
Gene Name | CLCN2 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 898 | |
Subcellular Localization |
Cell membrane Multi-pass membrane protein. |
|
Protein Description | Voltage-gated chloride channel. Chloride channels have several functions including the regulation of cell volume; membrane potential stabilization, signal transduction and transepithelial transport.. | |
Protein Sequence | MAAAAAEEGMEPRALQYEQTLMYGRYTQDLGAFAKEEAARIRLGGPEPWKGPPSSRAAPELLEYGRSRCARCRVCSVRCHKFLVSRVGEDWIFLVLLGLLMALVSWVMDYAIAACLQAQQWMSRGLNTSILLQYLAWVTYPVVLITFSAGFTQILAPQAVGSGIPEMKTILRGVVLKEYLTLKTFIAKVIGLTCALGSGMPLGKEGPFVHIASMCAALLSKFLSLFGGIYENESRNTEMLAAACAVGVGCCFAAPIGGVLFSIEVTSTFFAVRNYWRGFFAATFSAFIFRVLAVWNRDEETITALFKTRFRLDFPFDLQELPAFAVIGIASGFGGALFVYLNRKIVQVMRKQKTINRFLMRKRLLFPALVTLLISTLTFPPGFGQFMAGQLSQKETLVTLFDNRTWVRQGLVEELEPPSTSQAWNPPRANVFLTLVIFILMKFWMSALATTIPVPCGAFMPVFVIGAAFGRLVGESMAAWFPDGIHTDSSTYRIVPGGYAVVGAAALAGAVTHTVSTAVIVFELTGQIAHILPVMIAVILANAVAQSLQPSLYDSIIRIKKLPYLPELGWGRHQQYRVRVEDIMVRDVPHVALSCTFRDLRLALHRTKGRMLALVESPESMILLGSIERSQVVALLGAQLSPARRRQHMQERRATQTSPLSDQEGPPTPEASVCFQVNTEDSAFPAARGETHKPLKPALKRGPSVTRNLGESPTGSAESAGIALRSLFCGSPPPEAASEKLESCEKRKLKRVRISLASDADLEGEMSPEEILEWEEQQLDEPVNFSDCKIDPAPFQLVERTSLHKTHTIFSLLGVDHAYVTSIGRLIGIVTLKELRKAIEGSVTAQGVKVRPPLASFRDSATSSSDTETTEVHALWGPHSRHGLPREGSPSDSDDKCQ | |
Overview of Protein Modification Sites with Functional and Structural Information | ||
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
2 | Acetylation | ------MAAAAAEEG ------CCHHHHHCC | 13.05 | 22814378 | |
20 | Phosphorylation | RALQYEQTLMYGRYT CHHHHHHHHHHCCCC | 11.10 | 25159151 | |
23 | Phosphorylation | QYEQTLMYGRYTQDL HHHHHHHHCCCCCCH | 11.10 | 28857561 | |
35 (in isoform 3) | Ubiquitination | - | 50.03 | 21906983 | |
35 (in isoform 1) | Ubiquitination | - | 50.03 | 21906983 | |
35 | Ubiquitination | QDLGAFAKEEAARIR CCHHHHHHHHHHHHC | 50.03 | 22817900 | |
76 | Phosphorylation | CARCRVCSVRCHKFL CCCCCCCCCCCHHHH | 15.11 | 22817900 | |
134 | Phosphorylation | NTSILLQYLAWVTYP CHHHHHHHHHHHCCC | 9.80 | 30257219 | |
146 | Phosphorylation | TYPVVLITFSAGFTQ CCCCCEEEECCCHHH | 13.84 | 30257219 | |
148 | Phosphorylation | PVVLITFSAGFTQIL CCCEEEECCCHHHHH | 20.87 | 30257219 | |
193 | Phosphorylation | IAKVIGLTCALGSGM HHHHHHHHHHHCCCC | 7.19 | - | |
308 | Phosphorylation | TITALFKTRFRLDFP HHHHHEEEEEECCCC | 27.92 | - | |
555 | Phosphorylation | LQPSLYDSIIRIKKL CCHHHHHHHHHHHCC | 13.32 | 24719451 | |
564 | Phosphorylation | IRIKKLPYLPELGWG HHHHCCCCCCCCCCC | 45.37 | 30576142 | |
607 | Phosphorylation | LRLALHRTKGRMLAL HHHHHHHCCCCEEEE | 27.40 | 24719451 | |
617 | Phosphorylation | RMLALVESPESMILL CEEEEEECCCCEEEE | 26.87 | - | |
641 | Phosphorylation | ALLGAQLSPARRRQH HHHCCCCCHHHHHHH | 12.39 | 29214152 | |
693 | Acetylation | AARGETHKPLKPALK CCCCCCCCCCCHHHH | 60.51 | 18603625 | |
696 | Acetylation | GETHKPLKPALKRGP CCCCCCCCHHHHCCC | 36.45 | 18603633 | |
704 | Phosphorylation | PALKRGPSVTRNLGE HHHHCCCCCCCCCCC | 38.66 | 28985074 | |
706 | Phosphorylation | LKRGPSVTRNLGESP HHCCCCCCCCCCCCC | 20.41 | 27794612 | |
712 | Phosphorylation | VTRNLGESPTGSAES CCCCCCCCCCCCHHH | 26.43 | 29255136 | |
714 | Phosphorylation | RNLGESPTGSAESAG CCCCCCCCCCHHHHC | 53.71 | 29255136 | |
716 | Phosphorylation | LGESPTGSAESAGIA CCCCCCCCHHHHCHH | 31.20 | 29255136 | |
719 | Phosphorylation | SPTGSAESAGIALRS CCCCCHHHHCHHHHH | 31.35 | 25159151 | |
726 | Phosphorylation | SAGIALRSLFCGSPP HHCHHHHHHHCCCCC | 27.01 | 21712546 | |
731 | Phosphorylation | LRSLFCGSPPPEAAS HHHHHCCCCCHHHHH | 35.10 | 21815630 | |
738 | Phosphorylation | SPPPEAASEKLESCE CCCHHHHHHHHHHHH | 42.17 | 21712546 | |
743 | Phosphorylation | AASEKLESCEKRKLK HHHHHHHHHHHHCCC | 37.70 | 21712546 | |
758 | Phosphorylation | RVRISLASDADLEGE CEEEECCCCCCCCCC | 38.33 | - | |
801 | Phosphorylation | PFQLVERTSLHKTHT CCEEEECCCCCCCHH | 23.33 | 22210691 | |
802 | Phosphorylation | FQLVERTSLHKTHTI CEEEECCCCCCCHHH | 34.40 | 22210691 | |
831 | Phosphorylation | GRLIGIVTLKELRKA HHHHEEEEHHHHHHH | 30.14 | 22210691 | |
856 | Phosphorylation | KVRPPLASFRDSATS EECCCCHHCCCCCCC | 28.62 | 24719451 | |
860 | Phosphorylation | PLASFRDSATSSSDT CCHHCCCCCCCCCCC | 29.23 | 30576142 | |
863 | Phosphorylation | SFRDSATSSSDTETT HCCCCCCCCCCCCCE | 27.79 | 30576142 | |
865 | Phosphorylation | RDSATSSSDTETTEV CCCCCCCCCCCCEEE | 48.60 | 28985074 | |
869 | Phosphorylation | TSSSDTETTEVHALW CCCCCCCCEEEEECC | 30.28 | 30576142 | |
889 | Phosphorylation | HGLPREGSPSDSDDK CCCCCCCCCCCCCCC | 19.24 | 28102081 | |
891 | Phosphorylation | LPREGSPSDSDDKCQ CCCCCCCCCCCCCCC | 51.98 | 28102081 | |
893 | Phosphorylation | REGSPSDSDDKCQ-- CCCCCCCCCCCCC-- | 52.63 | 28102081 |
Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
---|---|---|---|---|---|---|
Oops, there are no upstream regulatory protein records of CLCN2_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of CLCN2_HUMAN !! |
* Distance = the distance between SAP position and PTM sites.
Modified Location | Modification | Variant Position (Distance <= 10) |
Residue Change | SAP | Related Disease | Reference |
---|---|---|---|---|---|---|
Oops, there are no SNP-PTM records of CLCN2_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
IF4G1_HUMAN | EIF4G1 | physical | 26496610 | |
NVL_HUMAN | NVL | physical | 26496610 | |
PEX10_HUMAN | PEX10 | physical | 26496610 | |
SRP14_HUMAN | SRP14 | physical | 26496610 | |
SRSF8_HUMAN | SRSF8 | physical | 26496610 | |
RFIP2_HUMAN | RAB11FIP2 | physical | 26496610 | |
KLDC2_HUMAN | KLHDC2 | physical | 26496610 | |
GPKOW_HUMAN | GPKOW | physical | 26496610 | |
ZCH10_HUMAN | ZCCHC10 | physical | 26496610 | |
CCD94_HUMAN | CCDC94 | physical | 26496610 | |
MUC13_HUMAN | MUC13 | physical | 26496610 | |
SNIP1_HUMAN | SNIP1 | physical | 26496610 | |
ZN668_HUMAN | ZNF668 | physical | 26496610 | |
F192A_HUMAN | FAM192A | physical | 26496610 | |
TOE1_HUMAN | TOE1 | physical | 26496610 | |
TDIF1_HUMAN | DNTTIP1 | physical | 26496610 | |
CA052_HUMAN | C1orf52 | physical | 26496610 |
Kegg Disease | |
---|---|
H00808 | Idiopathic generalized epilepsies (IGEs), including: Childhood absence epilepsy (CAE); Juvenile abse |
OMIM Disease | |
607628 | Epilepsy, idiopathic generalized 11 (EIG11) |
607628 | Juvenile absence epilepsy 2 (JAE2) |
607628 | Juvenile myoclonic epilepsy 8 (EJM8) |
615651 | Leukoencephalopathy with ataxia (LKPAT) |
Kegg Drug | |
There are no disease associations of PTM sites. | |
DrugBank | |
DB01046 | Lubiprostone |
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