Structure of PDB 1gax Chain B Binding Site BS04
Receptor Information
>1gax Chain B (length=862) Species:
274
(Thermus thermophilus) [
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MDLPKAYDPKSVEPKWAEKWAKNPFVANPKSGKPPFVIFMPPPNVTGSLH
MGHALDNSLQDALIRYKRMRGFEAVWLPGTDHAGIATQVVVERLLLKEGK
TRHDLGREKFLERVWQWKEESGGTILKQLKRLGASADWSREAFTMDEKRS
RAVRYAFSRYYHEGLAYRAPRLVNWCPRCETTLSDLEVETEPTPGKLYTL
RYEVEGGGFIEIATVRPETVFADQAIAVHPEDERYRHLLGKRARIPLTEV
WIPILADPAVEKDFGTGALKVTPAHDPLDYEIGERHGLKPVSVINLEGRM
EGERVPEALRGLDRFEARRKAVELFREAGHLVKEEDYTIALATCSRCGTP
IEYAIFPQWWLRMRPLAEEVLKGLRRGDIAFVPERWKKVNMDWLENVKDW
NISRQLWWGHQIPAWYCEDCQAVNVPRPERYLEDPTSCEACGSPRLKRDE
DVFDTWFSSALWPLSTLGWPEETEDLKAFYPGDVLVTGYDILFLWVSRME
VSGYHFMGERPFKTVLLHGLVLDEKGQKMSKSKGNVIDPLEMVERYGADA
LRFALIYLATGGQDIRLDLRWLEMARNFANKLYNAARFVLLSREGFQAKE
DTPTLADRFMRSRLSRGVEEITALYEALDLAQAAREVYELVWSEFCDWYL
EAAKPALKAGNAHTLRTLEEVLAVLLKLLHPMMPFLTSELYQALTGKEEL
ALEAWPEPGGRDEEAERAFEALKQAVTAVRALKAEAGLPPAQEVRVYLEG
ETAPVEENLEVFRFLSRADLLPERPAKALVKAMPRVTARMPLEGLLDVEE
WRRRQEKRLKELLALAERSQRKLASPGFREKAPKEVVEAEEARLKENLEQ
AERIREALSQIG
Ligand information
Ligand ID
VAA
InChI
InChI=1S/C15H24N8O6S/c1-6(2)8(16)14(26)22-30(27,28)21-3-7-10(24)11(25)15(29-7)23-5-20-9-12(17)18-4-19-13(9)23/h4-8,10-11,15,21,24-25H,3,16H2,1-2H3,(H,22,26)(H2,17,18,19)/t7-,8+,10-,11-,15-/m1/s1
InChIKey
ILBDFTSSTCBHRF-CYUGOOACSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(C)[C@H](N)C(=O)N[S](=O)(=O)NC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
ACDLabs 10.04
O=C(NS(=O)(=O)NCC3OC(n2cnc1c(ncnc12)N)C(O)C3O)C(N)C(C)C
OpenEye OEToolkits 1.5.0
CC(C)[C@@H](C(=O)NS(=O)(=O)NC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O)N
OpenEye OEToolkits 1.5.0
CC(C)C(C(=O)NS(=O)(=O)NCC1C(C(C(O1)n2cnc3c2ncnc3N)O)O)N
CACTVS 3.341
CC(C)[CH](N)C(=O)N[S](=O)(=O)NC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
Formula
C15 H24 N8 O6 S
Name
N-[VALINYL]-N'-[ADENOSYL]-DIAMINOSUFONE
ChEMBL
DrugBank
ZINC
ZINC000031976707
PDB chain
1gax Chain B Residue 1990 [
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Receptor-Ligand Complex Structure
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PDB
1gax
Structural basis for double-sieve discrimination of L-valine from L-isoleucine and L-threonine by the complex of tRNA(Val) and valyl-tRNA synthetase.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
P41 P42 N44 H50 G52 H53 D81 W456 S459 T487 G488 D490 I491 W495 L520 V521
Binding residue
(residue number reindexed from 1)
P41 P42 N44 H50 G52 H53 D81 W456 S459 T487 G488 D490 I491 W495 L520 V521
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
C176 C179 C344 C347 W456 I491 W495 K528 K531
Catalytic site (residue number reindexed from 1)
C176 C179 C344 C347 W456 I491 W495 K528 K531
Enzyme Commision number
6.1.1.9
: valine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0002161
aminoacyl-tRNA editing activity
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004832
valine-tRNA ligase activity
GO:0005524
ATP binding
GO:0046872
metal ion binding
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006438
valyl-tRNA aminoacylation
GO:0106074
aminoacyl-tRNA metabolism involved in translational fidelity
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1gax
,
PDBe:1gax
,
PDBj:1gax
PDBsum
1gax
PubMed
11114335
UniProt
P96142
|SYV_THETH Valine--tRNA ligase (Gene Name=valS)
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