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5J5Z

Crystal structure of the D444V disease-causing mutant of the human dihydrolipoamide dehydrogenase

Functional Information from GO Data
ChainGOidnamespacecontents
A0001669cellular_componentacrosomal vesicle
A0004148molecular_functiondihydrolipoyl dehydrogenase activity
A0005515molecular_functionprotein binding
A0005634cellular_componentnucleus
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0005929cellular_componentcilium
A0005967cellular_componentobsolete mitochondrial pyruvate dehydrogenase complex
A0006086biological_processacetyl-CoA biosynthetic process from pyruvate
A0006120biological_processmitochondrial electron transport, NADH to ubiquinone
A0006508biological_processproteolysis
A0007369biological_processgastrulation
A0009083biological_processbranched-chain amino acid catabolic process
A0016491molecular_functionoxidoreductase activity
A0016668molecular_functionoxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
A0031410cellular_componentcytoplasmic vesicle
A0031514cellular_componentmotile cilium
A0034604molecular_functionpyruvate dehydrogenase (NAD+) activity
A0042391biological_processregulation of membrane potential
A0042995cellular_componentcell projection
A0043159cellular_componentacrosomal matrix
A0045240cellular_componentalpha-ketoacid dehydrogenase complex
A0045252cellular_componentoxoglutarate dehydrogenase complex
A0045254cellular_componentpyruvate dehydrogenase complex
A0047101molecular_functionbranched-chain alpha-keto acid dehydrogenase activity
A0048240biological_processsperm capacitation
A0050660molecular_functionflavin adenine dinucleotide binding
A0106077biological_processobsolete histone succinylation
A1902493cellular_componentacetyltransferase complex
B0001669cellular_componentacrosomal vesicle
B0004148molecular_functiondihydrolipoyl dehydrogenase activity
B0005515molecular_functionprotein binding
B0005634cellular_componentnucleus
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0005929cellular_componentcilium
B0005967cellular_componentobsolete mitochondrial pyruvate dehydrogenase complex
B0006086biological_processacetyl-CoA biosynthetic process from pyruvate
B0006120biological_processmitochondrial electron transport, NADH to ubiquinone
B0006508biological_processproteolysis
B0007369biological_processgastrulation
B0009083biological_processbranched-chain amino acid catabolic process
B0016491molecular_functionoxidoreductase activity
B0016668molecular_functionoxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
B0031410cellular_componentcytoplasmic vesicle
B0031514cellular_componentmotile cilium
B0034604molecular_functionpyruvate dehydrogenase (NAD+) activity
B0042391biological_processregulation of membrane potential
B0042995cellular_componentcell projection
B0043159cellular_componentacrosomal matrix
B0045240cellular_componentalpha-ketoacid dehydrogenase complex
B0045252cellular_componentoxoglutarate dehydrogenase complex
B0045254cellular_componentpyruvate dehydrogenase complex
B0047101molecular_functionbranched-chain alpha-keto acid dehydrogenase activity
B0048240biological_processsperm capacitation
B0050660molecular_functionflavin adenine dinucleotide binding
B0106077biological_processobsolete histone succinylation
B1902493cellular_componentacetyltransferase complex
Functional Information from PDB Data
site_idAC1
Number of Residues38
Detailsbinding site for residue FAD A 501
ChainResidue
AILE12
ATHR44
ACYS45
AVAL48
AGLY49
ACYS50
ALYS54
AGLY117
ATYR118
AGLY119
AALA147
AGLY13
ATHR148
AGLY149
ASER150
AILE189
AARG280
APHE283
AGLY319
AASP320
AMET326
ALEU327
AGLY15
AALA328
AHIS329
ATYR359
AHOH649
AHOH667
AHOH668
AHOH696
AHOH788
BHIS452
APRO16
AGLY17
AGLU36
ALYS37
AASN38
AGLY43

site_idAC2
Number of Residues6
Detailsbinding site for residue PO4 A 502
ChainResidue
AARG299
AARG301
AGLY324
AGOL504
AHOH622
AHOH797

site_idAC3
Number of Residues10
Detailsbinding site for residue GOL A 503
ChainResidue
ATHR284
AASN286
ALEU287
AGLY288
ALEU289
AGLU290
AGLU291
AHOH616
AHOH642
AHOH769

site_idAC4
Number of Residues8
Detailsbinding site for residue GOL A 504
ChainResidue
AARG301
AGLN409
ASER411
APO4502
AHOH644
AHOH658
AHOH676
AHOH845

site_idAC5
Number of Residues9
Detailsbinding site for residue GOL A 505
ChainResidue
AASP333
AHIS348
AASP350
ACYS353
AGLU437
AHOH601
AHOH621
AHOH624
BARG447

site_idAC6
Number of Residues39
Detailsbinding site for residue FAD B 501
ChainResidue
BASP320
BMET326
BLEU327
BALA328
BHIS329
BTYR359
BHOH605
BHOH628
BHOH655
BHOH656
BHOH721
AHIS452
BILE12
BGLY13
BGLY15
BPRO16
BGLY17
BILE35
BGLU36
BLYS37
BASN38
BGLY43
BTHR44
BCYS45
BVAL48
BGLY49
BCYS50
BLYS54
BGLY117
BTYR118
BGLY119
BALA147
BTHR148
BGLY149
BSER150
BILE189
BARG280
BPHE283
BGLY319

site_idAC7
Number of Residues4
Detailsbinding site for residue PO4 B 502
ChainResidue
BARG299
BARG301
BALA323
BGLY324

Functional Information from PROSITE/UniProt
site_idPS00076
Number of Residues11
DetailsPYRIDINE_REDOX_1 Pyridine nucleotide-disulphide oxidoreductases class-I active site. GGtCLnvGCIP
ChainResidueDetails
AGLY42-PRO52

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000250|UniProtKB:P09624
ChainResidueDetails
AHIS452
BHIS452

site_idSWS_FT_FI2
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:15946682
ChainResidueDetails
AGLU36
AMET326
BGLU36
BLYS54
BGLY119
BTHR148
BGLY185
BGLU208
BVAL243
BGLY279
BASP320
ALYS54
BMET326
AGLY119
ATHR148
AGLY185
AGLU208
AVAL243
AGLY279
AASP320

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: Important for interaction with PDHX and activity of multienzyme pyruvate dehydrogenase complex => ECO:0000269|PubMed:20385101
ChainResidueDetails
AASP413
ATYR438
BASP413
BTYR438

site_idSWS_FT_FI4
Number of Residues14
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:O08749
ChainResidueDetails
ALYS31
BLYS87
BLYS97
BLYS108
BLYS375
BLYS470
ALYS69
ALYS87
ALYS97
ALYS108
ALYS375
ALYS470
BLYS31
BLYS69

site_idSWS_FT_FI5
Number of Residues10
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:O08749
ChainResidueDetails
ALYS124
BLYS395
ALYS131
ALYS238
ALYS242
ALYS395
BLYS124
BLYS131
BLYS238
BLYS242

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:O08749
ChainResidueDetails
ASER250
BSER250

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q6P6R2
ChainResidueDetails
ASER262
BSER262

site_idSWS_FT_FI8
Number of Residues4
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:O08749
ChainResidueDetails
ALYS311
ALYS385
BLYS311
BLYS385

site_idSWS_FT_FI9
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS382
BLYS382

site_idSWS_FT_FI10
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163
ChainResidueDetails
ASER467
BSER467

218853

PDB entries from 2024-04-24

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