+ |
COX4I1 | up-regulates
|
Oxidative_phosphorylation |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253101 |
|
|
Mus musculus |
|
pmid |
sentence |
23021218 |
PGC1a is known to drive the expression of many genes involved in mitochondrial oxidative phosphorylation, including cytochrome c (CytC) and the cyto- chrome C oxidative (COX) subunits (CoxIII, Cox4il, Cox5b, Cox7a, and Cox8b). |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
PPARGC1A | up-regulates quantity by expression
transcriptional regulation
|
COX4I1 |
0.41 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253098 |
|
|
Mus musculus |
Adipocyte |
pmid |
sentence |
23021218 |
PGC1a is known to drive the expression of many genes involved in mitochondrial oxidative phosphorylation, including cytochrome c (CytC) and the cyto- chrome C oxidative (COX) subunits (CoxIII, Cox4il, Cox5b, Cox7a, and Cox8b). |
|
Publications: |
1 |
Organism: |
Mus Musculus |
+ |
COX4I1 | form complex
binding
|
Mitochondrial respiratory chain complex IV |
0.745 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-267744 |
|
|
|
|
pmid |
sentence |
30030361 |
Complex IV (EC 1.9.31) or cytochrome c oxidase (COX) catalyses the oxidation of cytochrome c and the reduction of oxygen to water, coupled to proton translocation [108]. Mammalian cIV contains 13 or 14 subunits |
|
Publications: |
1 |
+ |
MITRAC complex | up-regulates quantity
relocalization
|
COX4I1 |
0.364 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-272487 |
|
|
|
|
pmid |
sentence |
23260140 |
Each association relies on the supply of subunits from either the cytosol or the mitochondrial matrix, suggesting that human TIM21 ushers nuclear-encoded proteins to assembly intermediates. In agreement with this, assembly of the early cytochrome c oxidase subunit COX4-1 requires TIM21, whereas it is dispensable for late-assembling subunits. The finding that TIM21 also interacts with complex I intermediates points to a more general role of TIM21 in respiratory-chain assembly. Furthermore, TIM21 appears to be tightly connected to MITRAC15, which, in contrast to TIM23 and MITRAC12, coimmunoprecipitates with TIM21 under all tested conditions. MITRAC15 associates with MITRAC and is required for complex IV but also complex I assembly. |
|
Publications: |
1 |
+ |
FASTKD5 | up-regulates quantity by expression
transcriptional regulation
|
COX4I1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-261223 |
|
|
Homo sapiens |
|
pmid |
sentence |
25683715 |
FASTKD5 is required for maturing precursor mRNAs that are not flanked by tRNAs and that therefore cannot be processed by the canonical mRNA maturation pathway. Silencing FASTKD5 rendered mature COX I mRNA almost undetectable, which severely reduced the synthesis of COX I, resulting in a complex IV assembly defect. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |