P00338

GPTKB entity

Statements (53)
Predicate Object
gptkbp:instanceOf gptkb:protein
gptkbp:alternativeName gptkb:COX2
Cytochrome c oxidase polypeptide II
gptkbp:component Cytochrome c oxidase complex
gptkbp:encodedBy gptkb:MT-CO2
gptkbp:Entrez_Gene_ID 4513
gptkbp:enzymeCommissionNumber 1.9.3.1
gptkbp:function Electron transfer in mitochondrial respiratory chain
gptkbp:GO gptkb:GO:0008137
gptkb:GO:0004129
gptkb:GO:0005739
GO:0005743
GO:0006119
GO:0045275
GO:0045277
gptkbp:hasDiseaseAssociation gptkb:Leigh_syndrome
cardiomyopathy
Mitochondrial complex IV deficiency
gptkbp:hasEnsembl ENSG00000198712
gptkbp:hasPfam PF00116
gptkbp:hasReactome R-HSA-163200
gptkbp:hasRefSeqID NP_001859.1
gptkbp:hasSubunitInteraction Interacts with cytochrome c oxidase subunit 1
Interacts with cytochrome c oxidase subunit 3
gptkbp:HGNC_ID 7412
https://www.w3.org/2000/01/rdf-schema#label P00338
gptkbp:InterPro IPR002429
gptkbp:isEssential true
gptkbp:isMitochondrial true
gptkbp:KEGGID hsa:4513
gptkbp:length 227 amino acids
gptkbp:locatedOnChromosome MT
Mitochondrial DNA
gptkbp:molecularWeight 25,603 Da
gptkbp:OMIM 516040
gptkbp:organism gptkb:Bos_taurus
gptkb:Mus_musculus
gptkb:Homo_sapiens
gptkbp:PDB gptkb:5B1A
1OCC
2OCC
gptkbp:postTranslationalModification Phosphorylation
Acetylation
gptkbp:reviewedBy true
gptkbp:subcellularLocation gptkb:Mitochondrion_inner_membrane
gptkbp:UniProt_entry_name Cytochrome c oxidase subunit 2
gptkbp:UniProtID gptkb:P00338
gptkbp:bfsParent gptkb:EC_1.1.1.27
gptkb:1I10_(human_LDHA)
gptkb:LDH-A
gptkb:LDHA
gptkb:P00338_(human_LDHA)
gptkbp:bfsLayer 7