Structure of PDB 5izm Chain A Binding Site BS02
Receptor Information
>5izm Chain A (length=460) Species:
9606
(Homo sapiens) [
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GRRVNVNVGVLGHIDSGKTALARALSTTAITLDLGFSCFSVPLPARLRSS
PLLQVTLVDCPGHASLIRTIIGGAQIIDLMMLVIDVTKGMQTQSAECLVI
GQIACQKLVVVLNKIDLLPEGKRQAAIDKMTKKMQKTLENTKFRGAPIIP
VAAKPGGAPQGIPELIELLTSQISIPTRDPSGPFLMSVDHCFSIGTVMTG
TILSGSISLGDSVEIPALKVVKKVKSMQMFHMPITSAMQGDRLGICVTQF
DPKLLERGLVCAPESLHTVHAALISVEKIPYFRGPLQTKAKFHITVGHET
VMGRLMFFSPAPDNFDQEPILDSFNFSQEYLFQEQYLSPRQQWALVEFEK
PVTCPRLCLVIGSRLDADIHTNTCRLAFHGILLHGLEDRNYADSFLPRLK
VYKLKHKDDYSVQLFVGLKVHLSTGELGIIDSFKIHIPGGLLSLTFKRYV
FDTHKRMVQS
Ligand information
Ligand ID
GNP
InChI
InChI=1S/C10H17N6O13P3/c11-10-13-7-4(8(19)14-10)12-2-16(7)9-6(18)5(17)3(28-9)1-27-32(25,26)29-31(23,24)15-30(20,21)22/h2-3,5-6,9,17-18H,1H2,(H,25,26)(H3,11,13,14,19)(H4,15,20,21,22,23,24)/t3-,5-,6-,9-/m1/s1
InChIKey
UQABYHGXWYXDTK-UUOKFMHZSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=P(O)(O)NP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(NP(=O)(O)O)O)O)O)N=C(NC2=O)N
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(NP(=O)(O)O)O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)N[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[CH](O)[CH]3O
Formula
C10 H17 N6 O13 P3
Name
PHOSPHOAMINOPHOSPHONIC ACID-GUANYLATE ESTER
ChEMBL
CHEMBL1233085
DrugBank
DB02082
ZINC
ZINC000037868676
PDB chain
5izm Chain A Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
5izm
Crystal structures of the human elongation factor eEFSec suggest a non-canonical mechanism for selenocysteine incorporation.
Resolution
3.4 Å
Binding residue
(original residue number in PDB)
D17 G19 K20 T21 A22 T48 N146 K147 D149 L150 A185 A186 K187
Binding residue
(residue number reindexed from 1)
D15 G17 K18 T19 A20 T31 N113 K114 D116 L117 A152 A153 K154
Annotation score
3
Binding affinity
PDBbind-CN
: -logKd/Ki=5.92,Kd=1.2uM
Enzymatic activity
Catalytic site (original residue number in PDB)
D17 K20 T21 T48 H96
Catalytic site (residue number reindexed from 1)
D15 K18 T19 T31 H63
Enzyme Commision number
3.6.5.-
Gene Ontology
Molecular Function
GO:0000049
tRNA binding
GO:0003746
translation elongation factor activity
GO:0003924
GTPase activity
GO:0005525
GTP binding
GO:0016787
hydrolase activity
GO:0035368
selenocysteine insertion sequence binding
GO:0043021
ribonucleoprotein complex binding
Biological Process
GO:0001514
selenocysteine incorporation
GO:0006412
translation
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:1990904
ribonucleoprotein complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5izm
,
PDBe:5izm
,
PDBj:5izm
PDBsum
5izm
PubMed
27708257
UniProt
P57772
|SELB_HUMAN Selenocysteine-specific elongation factor (Gene Name=EEFSEC)
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