UniProt ID | NDUBB_HUMAN | |
---|---|---|
UniProt AC | Q9NX14 | |
Protein Name | NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial | |
Gene Name | NDUFB11 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 153 | |
Subcellular Localization |
Mitochondrion inner membrane Single-pass membrane protein . |
|
Protein Description | Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in 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.. | |
Protein Sequence | MAAGLFGLSARRLLAAAATRGLPAARVRWESSFSRTVVAPSAVAGKRPPEPTTPWQEDPEPEDENLYEKNPDSHGYDKDPVLDVWNMRLVFFFGVSIILVLGSTFVAYLPDYRMKEWSRREAERLVKYREANGLPIMESNCFDPSKIQLPEDE | |
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 |
---|---|---|---|---|---|
9 | O-linked_Glycosylation | AAGLFGLSARRLLAA CCCHHHHHHHHHHHH | 21.80 | 30379171 | |
12 | Dimethylation | LFGLSARRLLAAAAT HHHHHHHHHHHHHHH | 33.50 | - | |
12 | Methylation | LFGLSARRLLAAAAT HHHHHHHHHHHHHHH | 33.50 | 24377053 | |
36 | O-linked_Glycosylation | WESSFSRTVVAPSAV ECCCCCCEEECCHHH | 20.38 | OGP | |
36 | Phosphorylation | WESSFSRTVVAPSAV ECCCCCCEEECCHHH | 20.38 | 26437602 | |
41 | O-linked_Glycosylation | SRTVVAPSAVAGKRP CCEEECCHHHCCCCC | 26.15 | OGP | |
41 | Phosphorylation | SRTVVAPSAVAGKRP CCEEECCHHHCCCCC | 26.15 | 26437602 | |
46 | Ubiquitination | APSAVAGKRPPEPTT CCHHHCCCCCCCCCC | 52.58 | 22817900 | |
46 (in isoform 2) | Ubiquitination | - | 52.58 | 21890473 | |
51 (in isoform 1) | Ubiquitination | - | 47.55 | 21890473 | |
52 | Phosphorylation | GKRPPEPTTPWQEDP CCCCCCCCCCCCCCC | 43.77 | - | |
53 | Phosphorylation | KRPPEPTTPWQEDPE CCCCCCCCCCCCCCC | 32.99 | - | |
115 | Ubiquitination | YLPDYRMKEWSRREA HCCCHHCHHHHHHHH | 47.21 | - | |
125 (in isoform 2) | Ubiquitination | - | 2.68 | - | |
128 | Phosphorylation | EAERLVKYREANGLP HHHHHHHHHHHCCCC | 13.25 | 24927040 | |
139 | Phosphorylation | NGLPIMESNCFDPSK CCCCCEECCCCCHHH | 22.86 | 20833797 | |
145 | Phosphorylation | ESNCFDPSKIQLPED ECCCCCHHHCCCCCC | 44.21 | 29759185 | |
146 | Acetylation | SNCFDPSKIQLPEDE CCCCCHHHCCCCCCC | 39.60 | 26051181 |
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 NDUBB_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of NDUBB_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 NDUBB_HUMAN !! |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
300952 | Linear skin defects with multiple congenital anomalies 3 (LSDMCA3) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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