Structure of PDB 4lyf Chain C Binding Site BS01
Receptor Information
>4lyf Chain C (length=154) Species:
9606
(Homo sapiens) [
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TEYKLVVVGACGVGKSALTIQLIQNHFVSYRKQVVIDGETSLLDILDTAG
QEEYRDQYMRTGEGFLLVFAINNTKSFEDIHHYREQIKRVKDSEDVPMVL
VGNKSDLPSRTVDTKQAQDLARSYGIPFIETSAKTRQGVDDAFYTLVREI
RKHK
Ligand information
Ligand ID
GDP
InChI
InChI=1S/C10H15N5O11P2/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(25-9)1-24-28(22,23)26-27(19,20)21/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
QGWNDRXFNXRZMB-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.385
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 12.01
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
Formula
C10 H15 N5 O11 P2
Name
GUANOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL384759
DrugBank
DB04315
ZINC
ZINC000008215481
PDB chain
4lyf Chain C Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
4lyf
K-Ras(G12C) inhibitors allosterically control GTP affinity and effector interactions.
Resolution
1.568 Å
Binding residue
(original residue number in PDB)
G13 G15 K16 S17 A18 N116 K117 D119 S145 A146 K147
Binding residue
(residue number reindexed from 1)
G12 G14 K15 S16 A17 N103 K104 D106 S132 A133 K134
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.6.5.2
: small monomeric GTPase.
Gene Ontology
Molecular Function
GO:0003924
GTPase activity
GO:0005525
GTP binding
Biological Process
GO:0007165
signal transduction
Cellular Component
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:4lyf
,
PDBe:4lyf
,
PDBj:4lyf
PDBsum
4lyf
PubMed
24256730
UniProt
P01116
|RASK_HUMAN GTPase KRas (Gene Name=KRAS)
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