Structure of PDB 2zt5 Chain A Binding Site BS01
Receptor Information
>2zt5 Chain A (length=530) Species:
9606
(Homo sapiens) [
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IVDRAKMEDTLKRRFFYDQAFAIYGGVSGLYDFGPVGCALKNNIIQTWRQ
HFIQEEQILEIDCTMLTPEPVLKTSGHVDKFADFMVKDVKNGECFRADHL
LKAHLQKLMSDKKCSVEKKSEMESVLAQLDNYGQQELADLFVNYNVKSPI
TGNDLSPPVSFNLMFKTFIGPGGNMPGYLRPETAQGIFLNFKRLLEFNQG
KLPFAAAQIGNSFRNEISPRSGLIRVREFTMAEIEHFVDPSEKDHPKFQN
VADLHLYLYSAKAQVSGQSARKMRLGDAVEQGVINNTVLGYFIGRIYLYL
TKVGISPDKLRFRQHMENEMAHYACDCWDAESKTSYGWIEIVGCADRSCY
DLSCHARATKVPLVAEKPYVEEVVPNVIEPSFGLGRIMYTVFEHTFHVRE
GDEQRTFFSFPAVVAPFKCSVLPLSQNQEFMPFVKELSEALTRHGVSHKV
DDSSGSIGRRYARTDEIGVAFGVTIDFDTVNKTPHTATLRDRDSMRQIRA
EISELPSIVQDLANGNITWADVEARYPLFE
Ligand information
Ligand ID
B4P
InChI
InChI=1S/C20H28N10O19P4/c21-15-9-17(25-3-23-15)29(5-27-9)19-13(33)11(31)7(45-19)1-43-50(35,36)47-52(39,40)49-53(41,42)48-51(37,38)44-2-8-12(32)14(34)20(46-8)30-6-28-10-16(22)24-4-26-18(10)30/h3-8,11-14,19-20,31-34H,1-2H2,(H,35,36)(H,37,38)(H,39,40)(H,41,42)(H2,21,23,25)(H2,22,24,26)/t7-,8-,11-,12-,13-,14-,19-,20-/m1/s1
InChIKey
YOAHKNVSNCMZGQ-XPWFQUROSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@](=O)(O)O[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)O[P@](O)(=O)O[P@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)[C@@H](O)[C@H]3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)[CH](O)[CH]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)N
Formula
C20 H28 N10 O19 P4
Name
BIS(ADENOSINE)-5'-TETRAPHOSPHATE
ChEMBL
CHEMBL339385
DrugBank
ZINC
ZINC000096014967
PDB chain
2zt5 Chain A Residue 1101 [
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Receptor-Ligand Complex Structure
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PDB
2zt5
Crystal structures and biochemical analyses suggest unique mechanism and role for human GlyRS in Ap4A homeostasis
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
D146 R159 D193 R277 E279 R288 V289 F292 E403 I404 G526 R529
Binding residue
(residue number reindexed from 1)
D83 R96 D130 R214 E216 R225 V226 F229 E340 I341 G383 R386
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.7.7.-
6.1.1.14
: glycine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004081
bis(5'-nucleosyl)-tetraphosphatase (asymmetrical) activity
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004820
glycine-tRNA ligase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016740
transferase activity
GO:0016787
hydrolase activity
GO:0042802
identical protein binding
GO:0046983
protein dimerization activity
GO:0141192
ATP:ATP adenylyltransferase activity
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006426
glycyl-tRNA aminoacylation
GO:0015966
diadenosine tetraphosphate biosynthetic process
GO:0070150
mitochondrial glycyl-tRNA aminoacylation
Cellular Component
GO:0005576
extracellular region
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0005829
cytosol
GO:0030141
secretory granule
GO:0030424
axon
GO:0042995
cell projection
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2zt5
,
PDBe:2zt5
,
PDBj:2zt5
PDBsum
2zt5
PubMed
UniProt
P41250
|GARS_HUMAN Glycine--tRNA ligase (Gene Name=GARS1)
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