Structure of PDB 4ls0 Chain A Binding Site BS02
Receptor Information
>4ls0 Chain A (length=364) Species:
9606
(Homo sapiens) [
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GDERFYAEHLMPTLQGLLDPESAHRLAVRFTSLGLLPRARFQDSDMLEVR
VLGHKFRNPVGIAAGFDKHGEAVDGLYKMGFGFVEIGSVTPKPQEGNPRP
RVFRLPEDQAVINRYGFNSHGLSVVEHRLRARQQKQAKLTEDGLPLGVNL
GKNKTSVDAAEDYAEGVRVLGPLADYLVVNVSSPNTAGLRSLQGKAELRR
LLTKVLQERDGLRRVHRPAVLVKIAPDLTSQDKEDIASVVKELGIDGLIV
TNTTVSRPAGLQGALRSETGGLSGKPLRDLSTQTIREMYALTQGRVPIIG
VGGVSSGQDALEKIRAGASLVQLYTALTFWGPPVVGKVKRELEALLKEQG
FGGVTDAIGADHRR
Ligand information
Ligand ID
B3B
InChI
InChI=1S/C17H13N3OS/c21-11-15-9-5-4-8-14(15)10-18-20-17-19-16(12-22-17)13-6-2-1-3-7-13/h1-12H,(H,19,20)/b18-10+
InChIKey
IGARVLMWRSOJOY-VCHYOVAHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1ccc(cc1)c2csc(n2)NN=Cc3ccccc3C=O
OpenEye OEToolkits 1.7.6
c1ccc(cc1)c2csc(n2)N/N=C/c3ccccc3C=O
CACTVS 3.385
O=Cc1ccccc1C=NNc2scc(n2)c3ccccc3
CACTVS 3.385
O=Cc1ccccc1/C=N/Nc2scc(n2)c3ccccc3
ACDLabs 12.01
O=Cc3c(/C=N/Nc1nc(cs1)c2ccccc2)cccc3
Formula
C17 H13 N3 O S
Name
2-{(E)-[2-(4-phenyl-1,3-thiazol-2-yl)hydrazinylidene]methyl}benzaldehyde
ChEMBL
CHEMBL2178104
DrugBank
ZINC
ZINC000004087469
PDB chain
4ls0 Chain A Residue 413 [
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Receptor-Ligand Complex Structure
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PDB
4ls0
Crystal structure of human dihydroorotate dehydrogenase (DHODH) with DHO1B0033
Resolution
2.07 Å
Binding residue
(original residue number in PDB)
M43 P52 H56 A59 R136 Y356 L359 T360 P364
Binding residue
(residue number reindexed from 1)
M11 P20 H24 A27 R104 Y324 L327 T328 P332
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 K223 N252
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4ls0
,
PDBe:4ls0
,
PDBj:4ls0
PDBsum
4ls0
PubMed
UniProt
Q02127
|PYRD_HUMAN Dihydroorotate dehydrogenase (quinone), mitochondrial (Gene Name=DHODH)
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