Structure of PDB 5fr2 Chain B Binding Site BS01
Receptor Information
>5fr2 Chain B (length=178) Species:
9913
(Bos taurus) [
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VNYKPPAQKSIQEIQELDKDDESLRKYKEALLGRVSADPNVPNVVVTRLT
LVCSTAPGPLELDLTGDLESFKKQSFVLKEGVEYRIKISFRVNREIVSGM
KYIQHTYRKGVKIDKTDYMVGSYGPRAEEYEFLTPMEEAPKGMLARGSYN
IKSRFTDDDRTDHLSWEWNLTIKKEWKD
Ligand information
Ligand ID
FAR
InChI
InChI=1S/C15H26/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9,12H,7-8,10-11H2,1-5H3/b14-6+,15-12+
InChIKey
JXBSHSBNOVLGHF-BUJBXKITSA-N
SMILES
Software
SMILES
CACTVS 3.341
OpenEye OEToolkits 1.5.0
CC=C(C)CCC=C(C)CCC=C(C)C
OpenEye OEToolkits 1.5.0
C\C=C(/C)\CC\C=C(/C)\CCC=C(C)C
CACTVS 3.341
C\C=C(C)\CC\C=C(C)\CCC=C(C)C
ACDLabs 10.04
C(=C/C)(\CC/C=C(/CC/C=C(\C)C)C)C
Formula
C15 H26
Name
FARNESYL
ChEMBL
DrugBank
ZINC
PDB chain
5fr2 Chain A Residue 1190 [
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Receptor-Ligand Complex Structure
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PDB
5fr2
Structural and Mechanistic Insights Into the Regulation of the Fundamental Rho-Regulator Rhogdi Alpha by Lysine Acetylation.
Resolution
3.35 Å
Binding residue
(original residue number in PDB)
L77 L86 E87 F102 Y110 I112 Q130
Binding residue
(residue number reindexed from 1)
L51 L60 E61 F76 Y84 I86 Q104
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005094
Rho GDP-dissociation inhibitor activity
GO:0005096
GTPase activator activity
Biological Process
GO:0007266
Rho protein signal transduction
GO:0071526
semaphorin-plexin signaling pathway
Cellular Component
GO:0001772
immunological synapse
GO:0005737
cytoplasm
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:5fr2
,
PDBe:5fr2
,
PDBj:5fr2
PDBsum
5fr2
PubMed
26719334
UniProt
P19803
|GDIR1_BOVIN Rho GDP-dissociation inhibitor 1 (Gene Name=ARHGDIA)
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