| UniProt ID | NDUF5_HUMAN | |
|---|---|---|
| UniProt AC | Q5TEU4 | |
| Protein Name | Arginine-hydroxylase NDUFAF5, mitochondrial {ECO:0000305} | |
| Gene Name | NDUFAF5 {ECO:0000312|HGNC:HGNC:15899} | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 345 | |
| Subcellular Localization | Mitochondrion inner membrane . Peripherally localized on the matrix face of the mitochondrial inner membrane. | |
| Protein Description | Arginine hydroxylase involved in the assembly of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I, MT-ND1) at early stages. [PubMed: 18940309] | |
| Protein Sequence | MLRPAGLWRLCRRPWAARVPAENLGRREVTSGVSPRGSTSPRTLNIFDRDLKRKQKNWAARQPEPTKFDYLKEEVGSRIADRVYDIPRNFPLALDLGCGRGYIAQYLNKETIGKFFQADIAENALKNSSETEIPTVSVLADEEFLPFKENTFDLVVSSLSLHWVNDLPRALEQIHYILKPDGVFIGAMFGGDTLYELRCSLQLAETEREGGFSPHISPFTAVNDLGHLLGRAGFNTLTVDTDEIQVNYPGMFELMEDLQGMGESNCAWNRKALLHRDTMLAAAAVYREMYRNEDGSVPATYQIYYMIGWKYHESQARPAERGSATVSFGELGKINNLMPPGKKSQ | |
| Overview of Protein Modification Sites with Functional and Structural Information | ||
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* ASA = Accessible Surface Area
| Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
|---|---|---|---|---|---|
| 30 | Phosphorylation | NLGRREVTSGVSPRG HCCCCCCCCCCCCCC | 18.27 | - | |
| 31 | Phosphorylation | LGRREVTSGVSPRGS CCCCCCCCCCCCCCC | 42.23 | 22817900 | |
| 34 | Phosphorylation | REVTSGVSPRGSTSP CCCCCCCCCCCCCCC | 16.65 | 22817900 | |
| 67 | Acetylation | ARQPEPTKFDYLKEE HCCCCCCCHHHHHHH | 47.13 | 7683747 | |
| 72 | Ubiquitination | PTKFDYLKEEVGSRI CCCHHHHHHHHHHHH | 45.67 | 24816145 | |
| 77 | Phosphorylation | YLKEEVGSRIADRVY HHHHHHHHHHHHHHC | 26.20 | - | |
| 84 | Phosphorylation | SRIADRVYDIPRNFP HHHHHHHCCCCCCCC | 14.73 | 25839225 | |
| 109 | Ubiquitination | YIAQYLNKETIGKFF HHHHHCCHHHHHHHH | 54.35 | 22817900 | |
| 109 (in isoform 1) | Ubiquitination | - | 54.35 | 21890473 | |
| 114 | Ubiquitination | LNKETIGKFFQADIA CCHHHHHHHHHHHHH | 38.87 | 22817900 | |
| 286 | Phosphorylation | MLAAAAVYREMYRNE HHHHHHHHHHHHHCC | 8.98 | - | |
| 290 | Phosphorylation | AAVYREMYRNEDGSV HHHHHHHHHCCCCCC | 12.92 | - |
| 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 NDUF5_HUMAN !! | ||||||
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of NDUF5_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 NDUF5_HUMAN !! | ||||||
| Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
|---|---|---|---|---|
| PPM1E_HUMAN | PPM1E | physical | 26186194 | |
| XRCC2_HUMAN | XRCC2 | physical | 26186194 | |
| RA51D_HUMAN | RAD51D | physical | 26186194 | |
| HBB_HUMAN | HBB | physical | 26186194 | |
| NDUF5_HUMAN | NDUFAF5 | physical | 27499296 | |
| BOLA3_HUMAN | BOLA3 | physical | 27499296 | |
| NDUF8_HUMAN | C17orf89 | physical | 27499296 | |
| STAR7_HUMAN | STARD7 | physical | 27499296 | |
| ECH1_HUMAN | ECH1 | physical | 27499296 | |
| ATP5E_HUMAN | ATP5E | physical | 27499296 | |
| ACPM_HUMAN | NDUFAB1 | physical | 27499296 | |
| ATPG_HUMAN | ATP5C1 | physical | 27499296 | |
| XRCC2_HUMAN | XRCC2 | physical | 28514442 | |
| HBB_HUMAN | HBB | physical | 28514442 | |
| RA51D_HUMAN | RAD51D | physical | 28514442 | |
| PPM1E_HUMAN | PPM1E | physical | 28514442 | |
| FPPS_HUMAN | FDPS | physical | 28514442 | |
| CGL_HUMAN | CTH | physical | 28514442 |
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| H00473 | Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency ( | |||||
| OMIM Disease | ||||||
| 252010 | Mitochondrial complex I deficiency (MT-C1D) | |||||
| 256000 | Leigh syndrome (LS) | |||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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