Structure of PDB 4ef8 Chain A Binding Site BS02
Receptor Information
>4ef8 Chain A (length=313) Species:
5664
(Leishmania major) [
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SMSLQVNLLNNTFANPFMNAAGVMCTTTEELVAMTESASGSLVSKSCTPA
LREGNPTPRYQALPLGSINSMGLPNNGFDFYLAYAAEQHDYGKKPLFLSM
SGLSMRENVEMCKRLAAVATEKGVILELNLSCPNVPGKPQVAYDFDAMRQ
CLTAVSEVYPHSFGVKMPPYFDFAHFDAAAEILNEFPKVQFITCINSIGN
GLVIDAETESVVIKPKQGFGGLGGRYVLPTALANINAFYRRCPGKLIFGC
GGVYTGEDAFLHVLAGASMVQVGTALQEEGPSIFERLTSELLGVMAKKRY
QTLDEFRGKVRTL
Ligand information
Ligand ID
0FI
InChI
InChI=1S/C7H7NS/c9-6-8-7-4-2-1-3-5-7/h1-6H,(H,8,9)
InChIKey
UNRRVOATHRPYDX-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1ccc(cc1)NC=S
ACDLabs 12.01
CACTVS 3.370
S=CNc1ccccc1
Formula
C7 H7 N S
Name
N-phenylthioformamide;
PHENYL ISOTHIOCYANATE, bound form
ChEMBL
DrugBank
ZINC
PDB chain
4ef8 Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4ef8
Target sites for the design of anti-trypanosomatid drugs based on the structure of dihydroorotate dehydrogenase.
Resolution
1.56 Å
Binding residue
(original residue number in PDB)
L102 S103 M104 N107 C131 V140 C150
Binding residue
(residue number reindexed from 1)
L103 S104 M105 N108 C132 V141 C151
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K44 N68 L72 C131 N133 V134 K165 I194
Catalytic site (residue number reindexed from 1)
K45 N69 L73 C132 N134 V135 K166 I195
Enzyme Commision number
1.3.98.1
: dihydroorotate oxidase (fumarate).
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004152
dihydroorotate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:1990663
dihydroorotate dehydrogenase (fumarate) activity
Biological Process
GO:0006106
fumarate metabolic process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0006222
UMP biosynthetic process
GO:0044205
'de novo' UMP biosynthetic process
Cellular Component
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0097014
ciliary plasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4ef8
,
PDBe:4ef8
,
PDBj:4ef8
PDBsum
4ef8
PubMed
23116399
UniProt
Q4QEW7
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