Structure of PDB 1d3g Chain A Binding Site BS02
Receptor Information
>1d3g Chain A (length=360) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MATGDERFYAEHLMPTLQGLLDPESAHRLAVRFTSLGLLPFQDSDMLEVR
VLGHKFRNPVGIAAGFDKHGEAVDGLYKMGFGFVEIGSVTPKPQEGNPRP
RVFRLPEDQAVINRYGFNSHGLSVVEHRLRARQQKQAKLTEDGLPLGVNL
GKNKTSVDAAEDYAEGVRVLGPLADYLVVNVSSPNTAGLGKAELRRLLTK
VLQERDGLRRVHRPAVLVKIAPDLTSQDKEDIASVVKELGIDGLIVTNTT
VSRPAGLQGALRSETGGLSGKPLRDLSTQTIREMYALTQGRVPIIGVGGV
SSGQDALEKIRAGASLVQLYTALTFWGPPVVGKVKRELEALLKEQGFGGV
TDAIGADHRR
Ligand information
Ligand ID
FMN
InChI
InChI=1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1
InChIKey
FVTCRASFADXXNN-SCRDCRAPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)O)O)O)O
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O
ACDLabs 12.01
N=2C(=O)NC(=O)C3=Nc1cc(C)c(C)cc1N(C=23)CC(O)C(O)C(O)COP(=O)(O)O
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(O)=O)c2cc1C
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P](O)(O)=O)c2cc1C
Formula
C17 H21 N4 O9 P
Name
FLAVIN MONONUCLEOTIDE;
RIBOFLAVIN MONOPHOSPHATE
ChEMBL
CHEMBL1201794
DrugBank
DB03247
ZINC
ZINC000003831425
PDB chain
1d3g Chain A Residue 398 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1d3g
Structures of human dihydroorotate dehydrogenase in complex with antiproliferative agents.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
A96 G97 K100 S120 N145 N181 N212 K255 N284 T285 S305 G306 V333 G334 G335 L355 Y356 T357
Binding residue
(residue number reindexed from 1)
A64 G65 K68 S88 N113 N149 N180 K219 N248 T249 S269 G270 V297 G298 G299 L319 Y320 T321
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G119 N145 F149 S215 N217 T218 K255 N284
Catalytic site (residue number reindexed from 1)
G87 N113 F117 S183 N185 T186 K219 N248
Enzyme Commision number
1.3.5.2
: dihydroorotate dehydrogenase (quinone).
Gene Ontology
Molecular Function
GO:0004151
dihydroorotase activity
GO:0004152
dihydroorotate dehydrogenase activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:0106430
dihydroorotate dehydrogenase (quinone) activity
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0006225
UDP biosynthetic process
GO:0009220
pyrimidine ribonucleotide biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005829
cytosol
GO:0016020
membrane
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1d3g
,
PDBe:1d3g
,
PDBj:1d3g
PDBsum
1d3g
PubMed
10673429
UniProt
Q02127
|PYRD_HUMAN Dihydroorotate dehydrogenase (quinone), mitochondrial (Gene Name=DHODH)
[
Back to BioLiP
]