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6ADI

Crystal Structures of IDH2 R140Q in complex with AG-881

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0004450molecular_functionisocitrate dehydrogenase (NADP+) activity
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0005777cellular_componentperoxisome
A0005829cellular_componentcytosol
A0005975biological_processcarbohydrate metabolic process
A0006097biological_processglyoxylate cycle
A0006099biological_processtricarboxylic acid cycle
A0006102biological_processisocitrate metabolic process
A0006103biological_process2-oxoglutarate metabolic process
A0006739biological_processNADP metabolic process
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0046872molecular_functionmetal ion binding
A0051287molecular_functionNAD binding
A0070062cellular_componentextracellular exosome
B0000287molecular_functionmagnesium ion binding
B0004450molecular_functionisocitrate dehydrogenase (NADP+) activity
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0005777cellular_componentperoxisome
B0005829cellular_componentcytosol
B0005975biological_processcarbohydrate metabolic process
B0006097biological_processglyoxylate cycle
B0006099biological_processtricarboxylic acid cycle
B0006102biological_processisocitrate metabolic process
B0006103biological_process2-oxoglutarate metabolic process
B0006739biological_processNADP metabolic process
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0046872molecular_functionmetal ion binding
B0051287molecular_functionNAD binding
B0070062cellular_componentextracellular exosome
Functional Information from PDB Data
site_idAC1
Number of Residues19
Detailsbinding site for residue NDP A 501
ChainResidue
ALYS112
ATHR350
AVAL351
ATHR352
AARG353
AHIS354
ATHR366
AASN367
AHOH617
AHOH651
AHOH673
ATHR115
AILE116
ATHR117
AARG122
AASN136
AGLU345
AHIS348
AGLY349

site_idAC2
Number of Residues17
Detailsbinding site for residue 9UO A 502
ChainResidue
ATRP164
AVAL294
AVAL297
AASP312
AVAL315
AGLN316
AILE319
ALEU320
BTRP164
BVAL294
BVAL297
BTRP306
BASP312
BVAL315
BGLN316
BILE319
BLEU320

site_idAC3
Number of Residues16
Detailsbinding site for residue NDP B 501
ChainResidue
BLYS112
BALA114
BTHR115
BILE116
BTHR117
BARG122
BASN136
BGLU345
BHIS348
BGLY349
BTHR350
BVAL351
BARG353
BHIS354
BASN367
BHOH614

Functional Information from PROSITE/UniProt
site_idPS00470
Number of Residues20
DetailsIDH_IMDH Isocitrate and isopropylmalate dehydrogenases signature. NYDGDVqSDilAqgf.GSLGL
ChainResidueDetails
AASN310-LEU329

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues10
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:O75874
ChainResidueDetails
ATHR115
BASN367
AARG122
ALYS299
AGLY349
AASN367
BTHR115
BARG122
BLYS299
BGLY349

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P33198
ChainResidueDetails
ATHR117
BARG172
BASP291
BASP314
ASER134
AARG149
AARG172
AASP291
AASP314
BTHR117
BSER134
BARG149

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: Critical for catalysis => ECO:0000250|UniProtKB:P33198
ChainResidueDetails
ATYR179
ALYS251
BTYR179
BLYS251

site_idSWS_FT_FI4
Number of Residues12
DetailsMOD_RES: N6-acetyllysine => ECO:0000250|UniProtKB:P54071
ChainResidueDetails
ALYS45
BLYS199
BLYS280
BLYS400
ALYS48
ALYS69
ALYS199
ALYS280
ALYS400
BLYS45
BLYS48
BLYS69

site_idSWS_FT_FI5
Number of Residues12
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS67
BLYS272
BLYS275
BLYS442
ALYS155
ALYS263
ALYS272
ALYS275
ALYS442
BLYS67
BLYS155
BLYS263

site_idSWS_FT_FI6
Number of Residues16
DetailsMOD_RES: N6-succinyllysine; alternate => ECO:0000250|UniProtKB:P54071
ChainResidueDetails
ALYS80
BLYS106
BLYS166
BLYS180
BLYS193
BLYS256
BLYS282
BLYS384
ALYS106
ALYS166
ALYS180
ALYS193
ALYS256
ALYS282
ALYS384
BLYS80

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: N6-acetyllysine => ECO:0000269|PubMed:22416140
ChainResidueDetails
ALYS413
BLYS413

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PDB entries from 2024-07-10

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