2Q8H
Structure of pyruvate dehydrogenase kinase isoform 1 in complex with dichloroacetate (DCA)
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0004672 | molecular_function | protein kinase activity |
A | 0004740 | molecular_function | pyruvate dehydrogenase (acetyl-transferring) kinase activity |
A | 0005515 | molecular_function | protein binding |
A | 0005524 | molecular_function | ATP binding |
A | 0005739 | cellular_component | mitochondrion |
A | 0005759 | cellular_component | mitochondrial matrix |
A | 0006006 | biological_process | glucose metabolic process |
A | 0008283 | biological_process | cell population proliferation |
A | 0008631 | biological_process | intrinsic apoptotic signaling pathway in response to oxidative stress |
A | 0010510 | biological_process | regulation of pyruvate decarboxylation to acetyl-CoA |
A | 0010906 | biological_process | regulation of glucose metabolic process |
A | 0016301 | molecular_function | kinase activity |
A | 0016740 | molecular_function | transferase activity |
A | 0033554 | biological_process | cellular response to stress |
A | 0045254 | cellular_component | pyruvate dehydrogenase complex |
A | 0097411 | biological_process | hypoxia-inducible factor-1alpha signaling pathway |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE K A 437 |
Chain | Residue |
A | ALA50 |
A | ARG51 |
A | PHE52 |
A | ASN89 |
A | VAL402 |
A | TYR403 |
A | HOH526 |
site_id | AC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE TF4 A 438 |
Chain | Residue |
A | ARG188 |
A | ILE191 |
A | LEU87 |
A | TYR114 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 14 |
Details | Binding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | Modified residue: {"description":"Phosphotyrosine; by FGFR1","evidences":[{"source":"PubMed","id":"22195962","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphotyrosine; by FGFR1, ABL1, FLT3 and JAK2","evidences":[{"source":"PubMed","id":"22195962","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 1 |
Details | Modified residue: {"description":"Phosphothreonine","evidences":[{"source":"PubMed","id":"26942675","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 1 |
Details | Modified residue: {"description":"N6-succinyllysine","evidences":[{"source":"UniProtKB","id":"Q8BFP9","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1jm6 |
Chain | Residue | Details |
A | GLU279 | |
A | HIS275 |