Structure of PDB 1ije Chain A Binding Site BS01
Receptor Information
>1ije Chain A (length=438) Species:
4932
(Saccharomyces cerevisiae) [
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EKSHINVVVIGHVDSGKSTTTGHLIYKCGGIDKRTIEKFEKEAAELGKGS
FKYAWVLDKLKAERERGITIDIALWKFETPKYQVTVIDAPGHRDFIKNMI
TGTSQADCAILIIAGGVGEFEAGISKDGQTREHALLAFTLGVRQLIVAVN
KMDSVKWDESRFQEIVKETSNFIKKVGYNPKTVPFVPISGWNGDNMIEAT
TNAPWYKGWEKETKAGVVKGKTLLEAIDAIEQPSRPTDKPLRLPLQDVYK
IGGIGTVPVGRVETGVIKPGMVVTFAPAGVTTEVKSVEMHHEQLEQGVPG
DNVGFNVKNVSVKEIRRGNVCGDAKNDPPKGCASFNATVIVLNHPGQISA
GYSPVLDCHTAHIACRFDELLEKNDRRSGKKLEDHPKFLKSGDAALVKFV
PSKPMCVEAFSEYPPLGRFAVRDMRQTVAVGVIKSVDK
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
1ije Chain A Residue 507 [
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Receptor-Ligand Complex Structure
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PDB
1ije
Crystal structures of nucleotide exchange intermediates in the eEF1A-eEF1Balpha complex.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
G19 S21 T22 N153 K154 D156 S192 W194
Binding residue
(residue number reindexed from 1)
G16 S18 T19 N150 K151 D153 S189 W191
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D17 K20 S21 T72 H95
Catalytic site (residue number reindexed from 1)
D14 K17 S18 T69 H92
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0003746
translation elongation factor activity
GO:0003779
actin binding
GO:0003924
GTPase activity
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0019003
GDP binding
GO:0019901
protein kinase binding
GO:0043022
ribosome binding
GO:0051015
actin filament binding
GO:1904408
melatonin binding
Biological Process
GO:0001933
negative regulation of protein phosphorylation
GO:0006409
tRNA export from nucleus
GO:0006412
translation
GO:0006414
translational elongation
GO:0006417
regulation of translation
GO:0006469
negative regulation of protein kinase activity
GO:0034198
cellular response to amino acid starvation
GO:0051017
actin filament bundle assembly
Cellular Component
GO:0000329
fungal-type vacuole membrane
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0005840
ribosome
GO:0005853
eukaryotic translation elongation factor 1 complex
GO:0005856
cytoskeleton
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1ije
,
PDBe:1ije
,
PDBj:1ije
PDBsum
1ije
PubMed
11373622
UniProt
P02994
|EF1A_YEAST Elongation factor 1-alpha (Gene Name=TEF1)
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