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1D3H

HUMAN DIHYDROOROTATE DEHYDROGENASE COMPLEXED WITH ANTIPROLIFERATIVE AGENT A771726

Functional Information from GO Data
ChainGOidnamespacecontents
A0004151molecular_functiondihydroorotase activity
A0004152molecular_functiondihydroorotate dehydrogenase activity
A0005515molecular_functionprotein binding
A0005654cellular_componentnucleoplasm
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005743cellular_componentmitochondrial inner membrane
A0005829cellular_componentcytosol
A0005886cellular_componentplasma membrane
A0006207biological_process'de novo' pyrimidine nucleobase biosynthetic process
A0006221biological_processpyrimidine nucleotide biosynthetic process
A0006225biological_processUDP biosynthetic process
A0009220biological_processpyrimidine ribonucleotide biosynthetic process
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0016627molecular_functionoxidoreductase activity, acting on the CH-CH group of donors
A0044205biological_process'de novo' UMP biosynthetic process
A0106430molecular_functiondihydroorotate dehydrogenase (quinone) activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 400
ChainResidue
AARG245
AVAL247
AHIS248
AHOH660
AHOH703

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE ACT A 401
ChainResidue
AGLN315
AARG318
AHOH439
AHOH682
ALYS307
APRO308
AASP311
ATHR314

site_idAC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE A26 A 397
ChainResidue
AMET43
APRO52
AHIS56
AALA59
APHE98
AARG136
ATYR356
ALEU359
ATHR360
AGLY363
APRO364
AHOH516
AHOH603

site_idAC4
Number of Residues25
DetailsBINDING SITE FOR RESIDUE FMN A 398
ChainResidue
AALA95
AALA96
AGLY97
ALYS100
AGLY119
ASER120
AASN145
AASN181
AASN212
ALYS255
ATHR283
AASN284
ATHR285
ASER305
AGLY306
ALEU309
AVAL333
AGLY334
AGLY335
ALEU355
ATYR356
ATHR357
AORO399
AHOH402
AHOH410

site_idAC5
Number of Residues11
DetailsBINDING SITE FOR RESIDUE ORO A 399
ChainResidue
ALYS100
AASN145
ATYR147
AGLY148
APHE149
AASN212
ASER215
AASN217
AASN284
ATHR285
AFMN398

Functional Information from PROSITE/UniProt
site_idPS00911
Number of Residues20
DetailsDHODEHASE_1 Dihydroorotate dehydrogenase signature 1. GfveiGSVTpkpQeGNprPR
ChainResidueDetails
AGLY114-ARG133

site_idPS00912
Number of Residues21
DetailsDHODEHASE_2 Dihydroorotate dehydrogenase signature 2. IIGvGGVsSgqdAleKIrAGA
ChainResidueDetails
AILE330-ALA350

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues364
DetailsTOPO_DOM: Mitochondrial intermembrane => ECO:0000250
ChainResidueDetails
AALA31-ARG395

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Nucleophile
ChainResidueDetails
ASER214

site_idSWS_FT_FI3
Number of Residues9
DetailsBINDING: BINDING => ECO:0000269|PubMed:10673429, ECO:0000269|PubMed:16480261
ChainResidueDetails
AALA95
AGLY119
AVAL180
AVAL211
AVAL254
AVAL282
ASER305
AGLY334
ALEU355

site_idSWS_FT_FI4
Number of Residues3
DetailsBINDING:
ChainResidueDetails
AASP99
AILE144
ATHR283

Catalytic Information from CSA
site_idMCSA1
Number of Residues7
DetailsM-CSA 109
ChainResidueDetails
AILE144electrostatic stabiliser
AGLY148activator, electrostatic stabiliser, enhance reactivity, polar/non-polar interaction
ASER214electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar/non-polar interaction, proton acceptor, proton donor, proton relay
APRO216electrostatic stabiliser
AASN217activator, electrostatic stabiliser, enhance reactivity, hydrogen bond acceptor
AVAL254electrostatic stabiliser, hydrogen bond donor
ATHR283electrostatic stabiliser

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PDB entries from 2024-04-24

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