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5UE9

WT DHODB with orotate bound

Functional Information from GO Data
ChainGOidnamespacecontents
A0004152molecular_functiondihydroorotate dehydrogenase activity
A0004589molecular_functiondihydroorotate dehydrogenase (NAD+) 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
B0006221biological_processpyrimidine nucleotide biosynthetic process
B0009055molecular_functionelectron transfer activity
B0016491molecular_functionoxidoreductase activity
B0044205biological_process'de novo' UMP biosynthetic process
B0046872molecular_functionmetal ion binding
B0050660molecular_functionflavin adenine dinucleotide binding
B0051537molecular_function2 iron, 2 sulfur cluster binding
C0004152molecular_functiondihydroorotate dehydrogenase activity
C0004589molecular_functiondihydroorotate dehydrogenase (NAD+) activity
C0005737cellular_componentcytoplasm
C0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
C0006221biological_processpyrimidine nucleotide biosynthetic process
C0006222biological_processUMP biosynthetic process
C0016491molecular_functionoxidoreductase activity
C0016627molecular_functionoxidoreductase activity, acting on the CH-CH group of donors
C0044205biological_process'de novo' UMP biosynthetic process
D0006221biological_processpyrimidine nucleotide biosynthetic process
D0009055molecular_functionelectron transfer activity
D0016491molecular_functionoxidoreductase activity
D0044205biological_process'de novo' UMP biosynthetic process
D0046872molecular_functionmetal ion binding
D0050660molecular_functionflavin adenine dinucleotide binding
D0051537molecular_function2 iron, 2 sulfur cluster binding
Functional Information from PDB Data
site_idAC1
Number of Residues20
Detailsbinding site for residue FMN A 401
ChainResidue
ASER24
AASN197
ATHR198
ASER221
AGLY222
AMET247
AGLY248
AGLY249
AGLY270
ATHR271
AORO402
AGLY25
AHOH507
ALYS48
AALA49
AASN72
AASN104
AASN132
ALYS170
AILE196

site_idAC2
Number of Residues10
Detailsbinding site for residue ORO A 402
ChainResidue
ALYS48
AASN72
AALA73
AILE74
AGLY75
ALEU76
AASN132
AASN197
ATHR198
AFMN401

site_idAC3
Number of Residues3
Detailsbinding site for residue CL A 403
ChainResidue
ATHR51
AHIS53
AARG55

site_idAC4
Number of Residues16
Detailsbinding site for residue FAD B 301
ChainResidue
BARG53
BPRO54
BILE55
BSER56
BLEU70
BTYR71
BARG72
BSER78
BGLY79
BTHR80
BILE120
BGLU221
BSER222
BARG223
BMET224
BHOH407

site_idAC5
Number of Residues9
Detailsbinding site for residue FES B 302
ChainResidue
BALA225
BCYS226
BGLY227
BGLY229
BCYS231
BTYR232
BALA233
BCYS234
BCYS249

site_idAC6
Number of Residues6
Detailsbinding site for residue GOL B 303
ChainResidue
BGLY144
BPHE145
BASP170
BGLY178
BHIS179
BVAL180

site_idAC7
Number of Residues15
Detailsbinding site for residue FAD D 301
ChainResidue
DARG53
DPRO54
DILE55
DSER56
DLEU70
DTYR71
DARG72
DSER78
DGLY79
DTHR80
DILE120
DGLU221
DSER222
DARG223
DMET224

site_idAC8
Number of Residues9
Detailsbinding site for residue FES D 302
ChainResidue
DALA225
DCYS226
DGLY227
DGLY229
DALA230
DCYS231
DTYR232
DCYS234
DCYS249

site_idAC9
Number of Residues21
Detailsbinding site for residue FMN C 401
ChainResidue
CTHR198
CSER221
CGLY222
CMET247
CGLY248
CGLY249
CGLY270
CTHR271
CORO402
CHOH505
CALA23
CSER24
CGLY25
CLYS48
CALA49
CASN72
CASN104
CASN132
CLYS170
CILE196
CASN197

site_idAD1
Number of Residues8
Detailsbinding site for residue ORO C 402
ChainResidue
CASN72
CILE74
CGLY75
CLEU76
CASN132
CASN197
CTHR198
CFMN401

site_idAD2
Number of Residues7
Detailsbinding site for residue GOL C 403
ChainResidue
CARG55
CASN78
CPRO79
CHOH515
DASN243
DHIS244
DALA245

Functional Information from PROSITE/UniProt
site_idPS00911
Number of Residues20
DetailsDHODEHASE_1 Dihydroorotate dehydrogenase signature 1. GsimvKATTlhpRfGNptPR
ChainResidueDetails
AGLY43-ARG62

site_idPS00912
Number of Residues21
DetailsDHODEHASE_2 Dihydroorotate dehydrogenase signature 2. IIGmGGVeSaqdVleMYmAGA
ChainResidueDetails
AILE244-ALA264

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01211
ChainResidueDetails
BARG53
DGLY79
DCYS226
DCYS231
DCYS234
DCYS249
BLEU70
BGLY79
BCYS226
BCYS231
BCYS234
BCYS249
DARG53
DLEU70

site_idSWS_FT_FI2
Number of Residues22
DetailsBINDING: BINDING => ECO:0000250
ChainResidueDetails
ASER24
AGLY248
AGLY270
CSER24
CLYS48
CASN72
CASN104
CASN132
CLYS170
CILE196
CASN197
ALYS48
CGLY222
CGLY248
CGLY270
AASN72
AASN104
AASN132
ALYS170
AILE196
AASN197
AGLY222

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PDB entries from 2024-07-24

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