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2E6D

Crystal structure of Trypanosoma cruzi dihydroorotate dehydrogenase in complex with fumarate

Functional Information from GO Data
ChainGOidnamespacecontents
A0004152molecular_functiondihydroorotate dehydrogenase activity
A0005737cellular_componentcytoplasm
A0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
A0006221biological_processpyrimidine nucleotide biosynthetic process
A0006222biological_processUMP biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0016627molecular_functionoxidoreductase activity, acting on the CH-CH group of donors
A0044205biological_process'de novo' UMP biosynthetic process
A1990663molecular_functiondihydroorotate dehydrogenase (fumarate) activity
B0004152molecular_functiondihydroorotate dehydrogenase activity
B0005737cellular_componentcytoplasm
B0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
B0006221biological_processpyrimidine nucleotide biosynthetic process
B0006222biological_processUMP biosynthetic process
B0016491molecular_functionoxidoreductase activity
B0016627molecular_functionoxidoreductase activity, acting on the CH-CH group of donors
B0044205biological_process'de novo' UMP biosynthetic process
B1990663molecular_functiondihydroorotate dehydrogenase (fumarate) activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE NCO A 1351
ChainResidue
AGLN275
AGLU276
AGLY278
BGLN275
BGLU276

site_idAC2
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FMN A 1350
ChainResidue
ASER44
AASN67
AASN127
ALYS164
AVAL193
AASN194
AGLY221
AGLY222
AILE225
ACYS248
AGLY249
AGLY250
AGLY271
ATHR272
AFUM1352
AHOH1380
AHOH1389
AHOH1405
AHOH1406
AALA18
AALA19
AGLY20
ALYS43

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE FUM A 1352
ChainResidue
ALYS43
AMET69
AGLY70
ALEU71
AASN127
ACYS130
APRO131
AASN132
AASN194
AFMN1350
AHOH1421

site_idAC4
Number of Residues24
DetailsBINDING SITE FOR RESIDUE FMN B 2350
ChainResidue
BALA18
BALA19
BGLY20
BLYS43
BSER44
BASN67
BASN127
BLYS164
BVAL193
BASN194
BSER195
BGLY221
BGLY222
BILE225
BCYS248
BGLY249
BGLY250
BGLY271
BTHR272
BFUM2352
BHOH2369
BHOH2372
BHOH2376
BHOH2382

site_idAC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE FUM B 2352
ChainResidue
BLYS43
BMET69
BGLY70
BLEU71
BASN127
BCYS130
BPRO131
BASN132
BASN194
BFMN2350
BHOH2433

site_idAC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 1361
ChainResidue
ACYS31
AALA34
ASER35
AHOH1492
BCYS31
BSER35
BHOH2475

site_idAC7
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GOL A 1363
ChainResidue
ALYS214
AGLN215
APHE217
AHOH1441
AHOH1474
AHOH1562
AHOH1601
BILE171
BARG238
BARG239

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 1364
ChainResidue
ATHR176
BLEU80
BARG112
BHOH2383
BHOH2404

site_idAC9
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 1362
ChainResidue
BGLN215
BPHE217
BHOH2520
BHOH2570
AILE171
AARG239
BLYS214

site_idBC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL B 1365
ChainResidue
ALEU80
AARG112
AHOH1388
AHOH1407
BASP175
BTHR176
BHOH2380

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Nucleophile => ECO:0000250
ChainResidueDetails
ACYS130
BCYS130

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:18302934
ChainResidueDetails
AALA19
BGLY222
BGLY249
BGLY271
ALYS164
AVAL193
AGLY222
AGLY249
AGLY271
BALA19
BLYS164
BVAL193

site_idSWS_FT_FI3
Number of Residues10
DetailsBINDING:
ChainResidueDetails
ALYS43
BASN194
AASN67
AASN127
AASN132
AASN194
BLYS43
BASN67
BASN127
BASN132

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PDB entries from 2024-04-24

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