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2BXV

Dual binding mode of a novel series of DHODH inhibitors

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
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 A1397
ChainResidue
AARG245
AVAL247
AHIS248
AHOH2190
AHOH2191

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE ACT A1398
ChainResidue
AGLN315
AARG318
AHOH2192
ALYS307
APRO308
AASP311
ATHR314

site_idAC3
Number of Residues26
DetailsBINDING SITE FOR RESIDUE FMN A1399
ChainResidue
AALA95
AALA96
AGLY97
ALYS100
AGLY119
ASER120
AASN145
ATYR147
AASN181
AASN212
ALYS255
ATHR283
AASN284
ATHR285
ASER305
AGLY306
ALEU309
AVAL333
AGLY334
AGLY335
ALEU355
ATYR356
ATHR357
AORO1400
AHOH2170
AHOH2193

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE ORO A1400
ChainResidue
ALYS100
AASN145
ATYR147
AGLY148
APHE149
AASN212
ASER215
AASN217
AASN284
ATHR285
AFMN1399

site_idAC5
Number of Residues16
DetailsBINDING SITE FOR RESIDUE 3FT A1401
ChainResidue
ATYR38
ALEU42
ALEU46
AGLN47
AHIS56
AALA59
APHE62
ALEU67
ALEU68
APHE98
AARG136
ATYR356
ALEU359
ATHR360
APRO364
AHOH2062

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
ATHR32-ARG396

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Nucleophile
ChainResidueDetails
ASER215

site_idSWS_FT_FI3
Number of Residues9
DetailsBINDING: BINDING => ECO:0000269|PubMed:10673429, ECO:0000269|PubMed:16480261
ChainResidueDetails
AALA96
ASER120
AASN181
AASN212
ALYS255
ATHR283
AGLY306
AGLY335
ATYR356

site_idSWS_FT_FI4
Number of Residues3
DetailsBINDING:
ChainResidueDetails
ALYS100
AASN145
AASN284

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1h7x
ChainResidueDetails
ASER215
ATHR218
APHE149
ALYS255

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1h7x
ChainResidueDetails
ASER215

site_idMCSA1
Number of Residues7
DetailsM-CSA 109
ChainResidueDetails
AASN145electrostatic stabiliser
APHE149activator, electrostatic stabiliser, enhance reactivity, polar/non-polar interaction
ASER215electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, polar/non-polar interaction, proton acceptor, proton donor, proton relay
AASN217electrostatic stabiliser
ATHR218activator, electrostatic stabiliser, enhance reactivity, hydrogen bond acceptor
ALYS255electrostatic stabiliser, hydrogen bond donor
AASN284electrostatic stabiliser

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PDB entries from 2024-10-09

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