UniProt ID | NDUS8_HUMAN | |
---|---|---|
UniProt AC | O00217 | |
Protein Name | NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial | |
Gene Name | NDUFS8 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 210 | |
Subcellular Localization | Mitochondrion . | |
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). May donate electrons to ubiquinone.. | |
Protein Sequence | MRCLTTPMLLRALAQAARAGPPGGRSLHSSAVAATYKYVNMQDPEMDMKSVTDRAARTLLWTELFRGLGMTLSYLFREPATINYPFEKGPLSPRFRGEHALRRYPSGEERCIACKLCEAICPAQAITIEAEPRADGSRRTTRYDIDMTKCIYCGFCQEACPVDAIVEGPNFEFSTETHEELLYNKEKLLNNGDKWEAEIAANIQADYLYR | |
Overview of Protein Modification Sites with Functional and Structural Information | ||
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
5 | Phosphorylation | ---MRCLTTPMLLRA ---CCCCCHHHHHHH | 32.26 | 24043423 | |
6 | Phosphorylation | --MRCLTTPMLLRAL --CCCCCHHHHHHHH | 8.18 | 24043423 | |
38 | Phosphorylation | AVAATYKYVNMQDPE HHHHHHEECCCCCCC | 6.14 | - | |
49 | Ubiquitination | QDPEMDMKSVTDRAA CCCCCCHHHHHHHHH | 37.19 | 21906983 | |
49 | Methylation | QDPEMDMKSVTDRAA CCCCCCHHHHHHHHH | 37.19 | 23748837 | |
49 | 2-Hydroxyisobutyrylation | QDPEMDMKSVTDRAA CCCCCCHHHHHHHHH | 37.19 | - | |
52 | Phosphorylation | EMDMKSVTDRAARTL CCCHHHHHHHHHHHH | 27.19 | - | |
71 | Phosphorylation | LFRGLGMTLSYLFRE HHHHHCCHHHHHHCC | 15.68 | 20068231 | |
73 | Phosphorylation | RGLGMTLSYLFREPA HHHCCHHHHHHCCCC | 15.60 | 20068231 | |
74 | Phosphorylation | GLGMTLSYLFREPAT HHCCHHHHHHCCCCE | 16.99 | 20068231 | |
88 | Ubiquitination | TINYPFEKGPLSPRF EECCCCCCCCCCCCC | 67.23 | 22817900 | |
92 | Phosphorylation | PFEKGPLSPRFRGEH CCCCCCCCCCCCCHH | 19.70 | 24719451 | |
96 | Methylation | GPLSPRFRGEHALRR CCCCCCCCCHHHHHH | 51.36 | 115919197 | |
106 | Phosphorylation | HALRRYPSGEERCIA HHHHHCCCCCCCHHH | 50.32 | 26471730 | |
121 | Glutathionylation | CKLCEAICPAQAITI HHHHHHHCCCCCEEE | 2.70 | 22555962 | |
133 | Dimethylation | ITIEAEPRADGSRRT EEEEEECCCCCCCCC | 36.49 | - | |
133 | Methylation | ITIEAEPRADGSRRT EEEEEECCCCCCCCC | 36.49 | 24377269 |
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 NDUS8_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of NDUS8_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 NDUS8_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
NDUV1_HUMAN | NDUFV1 | physical | 22939629 | |
NDUV2_HUMAN | NDUFV2 | physical | 22939629 | |
SURF1_HUMAN | SURF1 | physical | 22939629 | |
SAM50_HUMAN | SAMM50 | physical | 22939629 | |
PYRD_HUMAN | DHODH | physical | 22939629 | |
OPA1_HUMAN | OPA1 | physical | 22939629 | |
RLA0_HUMAN | RPLP0 | physical | 22939629 | |
PSN1_HUMAN | PSEN1 | physical | 22939629 | |
RAB5B_HUMAN | RAB5B | physical | 22939629 | |
AFG32_HUMAN | AFG3L2 | physical | 26344197 | |
CY1_HUMAN | CYC1 | physical | 26344197 | |
NDUAC_HUMAN | NDUFA12 | physical | 26344197 | |
NDUS3_HUMAN | NDUFS3 | physical | 26344197 | |
PHB2_HUMAN | PHB2 | physical | 26344197 | |
RAB1A_HUMAN | RAB1A | physical | 26344197 | |
RAB1B_HUMAN | RAB1B | physical | 26344197 | |
SDHB_HUMAN | SDHB | physical | 26344197 | |
QCR2_HUMAN | UQCRC2 | physical | 26344197 | |
QCR8_HUMAN | UQCRQ | physical | 26344197 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
256000 | Leigh syndrome (LS) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
loading...