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ProteomicsOGDH/DHTKD1-DLST (E1o/E1a- E2o) CL-MS
human OGDH (E1o) and DHTKD1 (E1a) were cross-linked with DLST (E2o). The samples were analyzed by LC-MS/MS in order to elucidate the interaction sites between these two E1-E2 subcomplexes.
ORGANISM(S): Homo sapiens (Human) Escherichia coli 
2021-09-10 | PXD023525 | Pride
Dhtkd1 Ogdh 
ProteomicsCL-MS OF hE1a (DHTKD1) or G729R hE1a with hE2o
CL-MS OF hE1a (DHTKD1) or G729R hE1a with hE2o to identify the possible difference in the interactions between hE1a-hE2o and G729R hE1a-hE2o
ORGANISM(S): Homo sapiens (Human) 
2020-04-22 | PXD017792 | Pride
2-oxoadipate dehydrogenase Dhtkd1 
TranscriptomicsGene expression signature of DHTKD1 gene knock-out spinal cord
We employed whole genome microarray expression profiling as a discovery platform to identify gene expression changes after DHTKD1 knock-out RNAs of spinal cords of 8-weeks-old wild-type (n=3) and DHTKD1 knock-out mice (n=3) were used to identify gene expression.
ORGANISM(S): Mus musculus 
2022-09-12 | GSE81735 | GEO
UnknownDHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice.
Not available
S-EPMC6002691 | biostudies-literature
UnknownInhibition and Crystal Structure of the Human DHTKD1-Thiamin Diphosphate Complex.
Not available
S-EPMC7890914 | biostudies-literature
UnknownHeterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients.
Not available
S-EPMC8774751 | biostudies-literature
UnknownCrystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolism.
Not available
S-EPMC7340257 | biostudies-literature
UnknownWhole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis.
Not available
S-EPMC5931135 | biostudies-literature
UnknownA nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.
Not available
S-EPMC3516600 | biostudies-literature
Genomics
DHTKD1 exon deletion associated with sporadic cerebellar ataxia
PRJNA1434322 | ENA
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