Structure of PDB 4lnb Chain B Binding Site BS01
Receptor Information
>4lnb Chain B (length=447) Species:
330879
(Aspergillus fumigatus Af293) [
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VHPGIPALFREPPLIHDLLSTETTELQSETVNKCLPLLKGIHNSQKGPFN
KYGIPALQRKDHLEYLYDSLEDYPASFVALDASRPWMVYWALAGLCLLGE
DVTRFRERVISTFTAAQNSTGGIGGGHGQMSHVASSYAAVLSIAMVGGEE
AFKLIDRKAMWKWLGKLKQPDGGFTVCEGGEEDVRGAYCAMVVHALLDLP
LALPPEAEARQNGLETFTDGLPEYLSRCQTYEGGISGSPGSEAHGAYAFC
ALACLCLLGRPEVVVPRYMNIATLLPWLSARQYAPEGGFSGRTNKLVDGC
YSHWVGNCWPLVQAALDGTQPLARSSVGNLYSREGLTRYILSCCQCKLGG
LRDKPGKHPDSYHTCYALTGLSTVQYYHYCTDSSVSSKFSSAFSWKHDPN
FASDGQGSDIGVFTENDRLVPFHPIFVIPHKSAEDIRVWFENQSFDL
Ligand information
Ligand ID
FPP
InChI
InChI=1S/C15H28O7P2/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-21-24(19,20)22-23(16,17)18/h7,9,11H,5-6,8,10,12H2,1-4H3,(H,19,20)(H2,16,17,18)/b14-9+,15-11+
InChIKey
VWFJDQUYCIWHTN-YFVJMOTDSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(C)=CCCC(C)=CCCC(C)=CCO[P](O)(=O)O[P](O)(O)=O
ACDLabs 10.04
O=P(OC/C=C(/CC\C=C(/C)CC\C=C(/C)C)C)(OP(=O)(O)O)O
OpenEye OEToolkits 1.5.0
CC(=CCC/C(=C/CC/C(=C/CO[P@@](=O)(O)OP(=O)(O)O)/C)/C)C
CACTVS 3.341
CC(C)=CCCC(/C)=C/CCC(/C)=C/CO[P@](O)(=O)O[P](O)(O)=O
OpenEye OEToolkits 1.5.0
CC(=CCCC(=CCCC(=CCOP(=O)(O)OP(=O)(O)O)C)C)C
Formula
C15 H28 O7 P2
Name
FARNESYL DIPHOSPHATE
ChEMBL
CHEMBL69330
DrugBank
DB07780
ZINC
ZINC000012494625
PDB chain
4lnb Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
4lnb
Crystal structures of the fungal pathogen Aspergillus fumigatus protein farnesyltransferase complexed with substrates and inhibitors reveal features for antifungal drug design.
Resolution
1.752 Å
Binding residue
(original residue number in PDB)
R274 Y277 H333 A335 R381 K384 Y390 W393
Binding residue
(residue number reindexed from 1)
R185 Y188 H244 A246 R292 K295 Y301 W304
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H333 R381 K384 D387 C389 Y390 D445 D452 H455
Catalytic site (residue number reindexed from 1)
H244 R292 K295 D298 C300 Y301 D353 D360 H363
Enzyme Commision number
2.5.1.58
: protein farnesyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004659
prenyltransferase activity
GO:0004660
protein farnesyltransferase activity
GO:0008270
zinc ion binding
GO:0008318
protein prenyltransferase activity
GO:0016853
isomerase activity
GO:0046872
metal ion binding
Biological Process
GO:0018343
protein farnesylation
GO:0097354
prenylation
Cellular Component
GO:0005965
protein farnesyltransferase complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4lnb
,
PDBe:4lnb
,
PDBj:4lnb
PDBsum
4lnb
PubMed
24347326
UniProt
Q4WPS9
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