Structure of PDB 4rxd Chain A Binding Site BS02
Receptor Information
>4rxd Chain A (length=355) Species:
5691
(Trypanosoma brucei) [
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MQMFMQVYDEIQMFLLEELELKFDMDPNRVRYLRKMMDTTCLGGKYNRGL
TVIDVAESLLSDGARRKRVLHDACVCGWMIEFLQAHYLVEDDIMDNSVTR
RGKPCWYRHPDVTVQCAINDGLLLKSWTHMMAMHFFADRPFLQDLLCRFN
RVDYTTAVGQLYDVTSMFDSNKLDPDVSQPTTTDFAEFTLSNYKRIVKYK
TAYYTYLLPLVMGLIVSEALPTVDMGVTEELAMLMGEYFQVQDDVMDCFT
PPERLGKVGTDIQDAKCSWLAVTFLAKASSAQVAEFKANYGSGDSEKVAT
VRRLYEEADLQGDYVAYEAAVAEQVKELIEKLRLCSPGFAASVETLWGKT
YKRQK
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
4rxd Chain A Residue 1403 [
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Receptor-Ligand Complex Structure
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PDB
4rxd
Farnesyl diphosphate synthase inhibitors with unique ligand-binding geometries.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D103 D107
Binding residue
(residue number reindexed from 1)
D91 D95
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K47 H98 D103 D107 R112 D175 K212 F251 D255 D256
Catalytic site (residue number reindexed from 1)
K45 H86 D91 D95 R100 D163 K200 F239 D243 D244
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004161
dimethylallyltranstransferase activity
GO:0004337
geranyltranstransferase activity
GO:0004659
prenyltransferase activity
GO:0016740
transferase activity
GO:0016765
transferase activity, transferring alkyl or aryl (other than methyl) groups
GO:0046872
metal ion binding
Biological Process
GO:0008299
isoprenoid biosynthetic process
GO:0045337
farnesyl diphosphate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4rxd
,
PDBe:4rxd
,
PDBj:4rxd
PDBsum
4rxd
PubMed
25815158
UniProt
Q86C09
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