Protein basic information
| LiverAtlas Protein ID |
HuLPr15319 |
|
Uniprot ID |
|
|
Uniprot Acc |
Q9HAC7;A4D1W5;B4DR73;Q4KMW4;Q4KMZ0;Q8TE00;Q8TEY1; |
|
Protein name |
CaiB/baiF CoA-transferase family protein C7orf10 |
|
Comment |
ALTERNATIVE PRODUCTS:Event=Alternative splicing; Named isoforms=3; Name=1; IsoId=Q9HAC7-1; Sequence=Displayed; Name=2; IsoId=Q9HAC7-2; Sequence=VSP 014721, VSP 014722; Note=No experimental confirmation available; Name=3; IsoId=Q9HAC7-3; Sequence=VSP 014722;||TISSUE SPECIFICITY:Highly expressed in kidney. Intermediate expression in liver, skeletal muscle and pancreas. Little to no expression detected in other tissues examined.||DISEASE:Defects in C7orf10 are the cause of glutaric aciduria type 3 (GA3) [MIM:231690]. GA3 is a metabolic disorder due to peroxisomal glutaryl-CoA oxidase deficiency and characterized by the excretion of abnormal quantities of glutaric acid but low 3- hydroxyglutaric acid.||SIMILARITY:Belongs to the CaiB/BaiF CoA-transferase family. |
|
Gene name |
|
|
Protein sequence
|
MPSETHAMLATLARVAALRRTCLFSGRGGGRGLWTGRPQS DMNNIKPLEGVKILDLTRVLAGPFATMNLGDLGAEVIKV ERPGAGDDTRTWGPPFVGTESTYYLSVNRNKKSIAVNIK DPKGVKIIKELAAVCDVFVENYVPGKLSAMGLGYEDIDE IAPHIIYCSITGYGQTGPISQRAGYDAVASAVSGLMHIT GPENGDPVRPGVAMTDLATGLYAYGAIMAGLIQKYKTGK GLFIDCNLLSSQVACLSHIAANYLIGQKEAKRWGTAHGS IVPYQAFKTKDGYIVVGAGNNQQFATVCKILDLPELIDN SKYKTNHLRVHNRKELIKILSERFEEELTSKWLYLFEGS GVPYGPINNMKNVFAEPQVLHNGLVMEMEHPTVGKISVP GPAVRYSKFKMSEARPPPLLGQHTTHILKEVLRYDDRAI GELLSAGVVDQHETH |
|
Database cross reference |
RefSeq Protein accession:NP_001180240
|
Liver relevance
|
HLPP validation |
Yes/No |
Yes |
|
Project name |
Chinese Liver;Human Liver Organelles; |
Ontology annotation
|
GO-F |
GO:0016740;F:transferase activity;IEA:UniProtKB-KW. |
Post-translational modification
| LiverAtlas Protein ID |
MOD type1 |
Position1 |
Residue1 |
Source name1 |
source ID1 |
Source method |
HLPP validation1 (Yes/no) |
Quality score |
|
HuLPr15319 |
PHOSPHORYLATION |
278 |
Y |
PhosphoSitePlus |
HTP |
N |
 
|
