UniProt ID | ECHD2_HUMAN | |
---|---|---|
UniProt AC | Q86YB7 | |
Protein Name | Enoyl-CoA hydratase domain-containing protein 2, mitochondrial | |
Gene Name | ECHDC2 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 292 | |
Subcellular Localization | Mitochondrion . | |
Protein Description | ||
Protein Sequence | MLRVLCLLRPWRPLRARGCASDGAAGGSEIQVRALAGPDQGITEILMNRPSARNALGNVFVSELLETLAQLREDRQVRVLLFRSGVKGVFCAGADLKEREQMSEAEVGVFVQRLRGLMNDIAAFPAPTIAAMDGFALGGGLELALACDLRVAASSAVMGLIETTRGLLPGAGGTQRLPRCLGVALAKELIFTGRRLSGTEAHVLGLVNHAVAQNEEGDAAYQRARALAQEILPQAPIAVRLGKVAIDRGTEVDIASGMAIEGMCYAQNIPTRDRLEGMAAFREKRTPKFVGK | |
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 |
---|---|---|---|---|---|
97 | Acetylation | FCAGADLKEREQMSE EECCCCHHHHHHHCH | 56.10 | - | |
97 | Succinylation | FCAGADLKEREQMSE EECCCCHHHHHHHCH | 56.10 | - | |
97 | Succinylation | FCAGADLKEREQMSE EECCCCHHHHHHHCH | 56.10 | - | |
103 | Phosphorylation | LKEREQMSEAEVGVF HHHHHHHCHHHHHHH | 33.09 | 28509920 | |
197 | Phosphorylation | IFTGRRLSGTEAHVL HHCCCCCCCCHHHHH | 41.69 | 20166139 | |
199 | Phosphorylation | TGRRLSGTEAHVLGL CCCCCCCCHHHHHHH | 26.99 | 20166139 |
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 ECHD2_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of ECHD2_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 ECHD2_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
A4_HUMAN | APP | physical | 21832049 | |
LSM8_HUMAN | LSM8 | physical | 21988832 | |
AUHM_HUMAN | AUH | physical | 26186194 | |
SLIRP_HUMAN | SLIRP | physical | 26186194 | |
TOP3A_HUMAN | TOP3A | physical | 26186194 | |
UQCC1_HUMAN | UQCC1 | physical | 26186194 | |
NDUS6_HUMAN | NDUFS6 | physical | 26186194 | |
CAF17_HUMAN | IBA57 | physical | 26186194 | |
CTU1_HUMAN | CTU1 | physical | 26186194 | |
DNLZ_HUMAN | DNLZ | physical | 26186194 | |
AUHM_HUMAN | AUH | physical | 28514442 | |
NDUS6_HUMAN | NDUFS6 | physical | 28514442 | |
HEM1_HUMAN | ALAS1 | physical | 28514442 | |
DNLZ_HUMAN | DNLZ | physical | 28514442 | |
SLIRP_HUMAN | SLIRP | physical | 28514442 | |
MMAB_HUMAN | MMAB | physical | 28514442 | |
CTU1_HUMAN | CTU1 | physical | 28514442 | |
TOP3A_HUMAN | TOP3A | physical | 28514442 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
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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