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3W22

Structure of Trypanosoma cruzi dihydroorotate dehydrogenase in complex with MII-3-125

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 Residues13
DetailsBINDING SITE FOR RESIDUE 2RO A 401
ChainResidue
ALYS43
ASER195
AGOL405
AFMN407
AHOH708
AASN53
AASN67
ASER68
AMET69
AGLY70
ALEU71
AASN127
AASN194

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 402
ChainResidue
ACYS31
AALA34
ASER35
APRO279
AHOH531
BCYS31
BSER35
BPRO279
BHOH643

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 403
ChainResidue
AILE171
AARG239
AHOH589
BLYS214
BPHE217

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 404
ChainResidue
ALYS214
APHE217
AHOH549
BILE171
BARG238
BARG239

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE GOL A 405
ChainResidue
ASER129
AGLN138
AASN194
ASER195
AGLY197
A2RO401
AHOH529

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 406
ChainResidue
APHE61
AVAL201
AASP203
AHOH572
AHOH637

site_idAC7
Number of Residues23
DetailsBINDING SITE FOR RESIDUE FMN A 407
ChainResidue
AALA18
AALA19
AGLY20
ALYS43
ASER44
ATYR58
AASN67
AASN127
ALYS164
AVAL193
AASN194
AGLY221
AGLY222
AILE225
ACYS248
AGLY249
AGLY250
AGLY271
ATHR272
A2RO401
AHOH507
AHOH516
AHOH527

site_idAC8
Number of Residues8
DetailsBINDING SITE FOR RESIDUE NCO A 408
ChainResidue
AGLN275
AGLU276
AGLY278
AHOH635
AHOH679
BGLN275
BGLU276
BGLY278

site_idAC9
Number of Residues12
DetailsBINDING SITE FOR RESIDUE 2RO B 401
ChainResidue
BLYS43
BARG50
BASN67
BMET69
BGLY70
BLEU71
BLEU101
BASN127
BASN194
BSER195
BFMN403
BHOH695

site_idBC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL B 402
ChainResidue
BASN194
BSER195
BGLY197
BGLY219
BHOH514
BHOH695

site_idBC2
Number of Residues21
DetailsBINDING SITE FOR RESIDUE FMN B 403
ChainResidue
BASN67
BASN127
BLYS164
BVAL193
BASN194
BSER195
BGLY222
BCYS248
BGLY249
BGLY250
BGLY271
BTHR272
B2RO401
BHOH506
BHOH517
BHOH522
BALA18
BALA19
BGLY20
BLYS43
BSER44

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Nucleophile","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues14
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"18302934","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues16
DetailsBinding site: {}
ChainResidueDetails

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PDB entries from 2025-12-24

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