| UniProt ID | NDUV2_HUMAN | |
|---|---|---|
| UniProt AC | P19404 | |
| Protein Name | NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial | |
| Gene Name | NDUFV2 | |
| Organism | Homo sapiens (Human). | |
| Sequence Length | 249 | |
| Subcellular Localization | Mitochondrion inner membrane. | |
| Protein Description | Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity).. | |
| Protein Sequence | MFFSAALRARAAGLTAHWGRHVRNLHKTVMQNGAGGALFVHRDTPENNPDTPFDFTPENYKRIEAIVKNYPEGHKAAAVLPVLDLAQRQNGWLPISAMNKVAEVLQVPPMRVYEVATFYTMYNRKPVGKYHIQVCTTTPCMLRNSDSILEAIQKKLGIKVGETTPDKLFTLIEVECLGACVNAPMVQINDNYYEDLTAKDIEEIIDELKAGKIPKPGPRSGRFSCEPAGGLTSLTEPPKGPGFGVQAGL | |
| 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 |
|---|---|---|---|---|---|
| 15 | Phosphorylation | RARAAGLTAHWGRHV HHHHHCCHHHHHHHH | 18.63 | 27251275 | |
| 32 | Ubiquitination | LHKTVMQNGAGGALF HHHHHHHCCCCCEEE | 24.96 | 24816145 | |
| 51 | Phosphorylation | TPENNPDTPFDFTPE CCCCCCCCCCCCCHH | 27.41 | - | |
| 61 | Acetylation | DFTPENYKRIEAIVK CCCHHHHHHHHHHHH | 59.49 | 26051181 | |
| 61 | 2-Hydroxyisobutyrylation | DFTPENYKRIEAIVK CCCHHHHHHHHHHHH | 59.49 | - | |
| 61 | Ubiquitination | DFTPENYKRIEAIVK CCCHHHHHHHHHHHH | 59.49 | 24816145 | |
| 68 | Malonylation | KRIEAIVKNYPEGHK HHHHHHHHHCCCCHH | 44.65 | 26320211 | |
| 70 | Phosphorylation | IEAIVKNYPEGHKAA HHHHHHHCCCCHHCH | 9.28 | 29496907 | |
| 113 | Phosphorylation | QVPPMRVYEVATFYT CCCCCEEEEEEEEEE | 8.36 | 24043423 | |
| 117 | Phosphorylation | MRVYEVATFYTMYNR CEEEEEEEEEECCCC | 23.50 | 24043423 | |
| 119 | Phosphorylation | VYEVATFYTMYNRKP EEEEEEEEECCCCCC | 6.04 | 24043423 | |
| 120 | Phosphorylation | YEVATFYTMYNRKPV EEEEEEEECCCCCCC | 14.69 | 25599653 | |
| 122 | Phosphorylation | VATFYTMYNRKPVGK EEEEEECCCCCCCCE | 12.19 | 24043423 | |
| 129 | Acetylation | YNRKPVGKYHIQVCT CCCCCCCEEEEEEEC | 33.61 | 25038526 | |
| 147 | Phosphorylation | CMLRNSDSILEAIQK HHCCCCHHHHHHHHH | 28.97 | 27251275 | |
| 154 | Acetylation | SILEAIQKKLGIKVG HHHHHHHHHHCCCCC | 43.80 | 25953088 | |
| 154 | 2-Hydroxyisobutyrylation | SILEAIQKKLGIKVG HHHHHHHHHHCCCCC | 43.80 | - | |
| 163 | Phosphorylation | LGIKVGETTPDKLFT HCCCCCCCCHHHEEE | 37.39 | 20068231 | |
| 164 | Phosphorylation | GIKVGETTPDKLFTL CCCCCCCCHHHEEEE | 25.78 | 20068231 | |
| 193 | Phosphorylation | VQINDNYYEDLTAKD EEECCCHHHCCCHHH | 14.82 | 22823520 | |
| 209 | Acetylation | EEIIDELKAGKIPKP HHHHHHHHCCCCCCC | 53.71 | 25038526 | |
| 209 | 2-Hydroxyisobutyrylation | EEIIDELKAGKIPKP HHHHHHHHCCCCCCC | 53.71 | - | |
| 209 | Ubiquitination | EEIIDELKAGKIPKP HHHHHHHHCCCCCCC | 53.71 | 29967540 | |
| 215 | Acetylation | LKAGKIPKPGPRSGR HHCCCCCCCCCCCCC | 67.11 | 2380383 | |
| 220 | Phosphorylation | IPKPGPRSGRFSCEP CCCCCCCCCCEECCC | 37.14 | - | |
| 233 | Phosphorylation | EPAGGLTSLTEPPKG CCCCCCCCCCCCCCC | 38.03 | - |
| Modified Location | Modified Residue | Modification | Type of Upstream Proteins | Gene Name of Upstream Proteins | UniProt AC of Upstream Proteins | Sources |
|---|---|---|---|---|---|---|
| 193 | Y | Phosphorylation | Kinase | SRC | P12931 | Uniprot |
| Modified Location | Modified Residue | Modification | Function | Reference | ||
|---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of NDUV2_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 NDUV2_HUMAN !! | ||||||
| Kegg Disease | ||||||
|---|---|---|---|---|---|---|
| H00473 | Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency ( | |||||
| OMIM Disease | ||||||
| There are no disease associations of PTM sites. | ||||||
| Kegg Drug | ||||||
| There are no disease associations of PTM sites. | ||||||
| DrugBank | ||||||
| There are no disease associations of PTM sites. | ||||||
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