Structure of PDB 3w3s Chain A Binding Site BS03
Receptor Information
>3w3s Chain A (length=527) Species:
190192
(Methanopyrus kandleri AV19) [
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MELKFSAEVELTLSREVDPAEIEPTVEEFVKEANEDLLQRGVPTGKEGAK
IESYYVLYDTIYMEITGTRYLRPHEAAMRVRKRLAERLGRKHRVGVRDLK
IPRYEVVLRFDREVTYDYVGYVPVADDVVVEDGTVRLTFQDVDEEMLRRH
VIDRVIRLVAWAVEERSELVERVTKVEPGTVVDESGPRRIRFRGDVTEEA
RRRGWVKEFPGRGQWIYTPPMAALFEVLRDFLLERVTRKLGFEPALFPKL
IPLETMFRMRYLHGLPDGMYYVCPPKRDPELFDDFKRELYVWGELNERTL
GSLKEKLRDPGYVLAPAQCEPFYELLRDEVVDPERLPIKLYDCSGWTYRW
EGGAAKGLERVNEFQRIEHVWIAEPEEAYRIRRELLEATKRVAEELELEW
KVVVSDDPFYLEGRLLEDRDIELPDVPSYEFEVYLPFKGERSSEEAWISV
GSFNVHGEHFVDGFNVKEKSGRTLFTGCAGLGVTRWVVGLLAQHGFYPYE
WPEPILERIDEKFGGLPEVPKTLTWPE
Ligand information
Ligand ID
SSA
InChI
InChI=1S/C13H19N7O8S/c14-5(1-21)12(24)19-29(25,26)27-2-6-8(22)9(23)13(28-6)20-4-18-7-10(15)16-3-17-11(7)20/h3-6,8-9,13,21-23H,1-2,14H2,(H,19,24)(H2,15,16,17)/t5-,6+,8+,9+,13+/m0/s1
InChIKey
HQXFJGONGJPTLZ-YTMOPEAISA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COS(=O)(=O)NC(=O)[C@H](CO)N)O)O)N
CACTVS 3.341
N[CH](CO)C(=O)N[S](=O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
CACTVS 3.341
N[C@@H](CO)C(=O)N[S](=O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
ACDLabs 10.04
O=C(NS(=O)(=O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O)C(N)CO
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COS(=O)(=O)NC(=O)C(CO)N)O)O)N
Formula
C13 H19 N7 O8 S
Name
5'-O-(N-(L-SERYL)-SULFAMOYL)ADENOSINE
ChEMBL
CHEMBL1163070
DrugBank
DB03869
ZINC
ZINC000013542770
PDB chain
3w3s Chain A Residue 2002 [
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Receptor-Ligand Complex Structure
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PDB
3w3s
Tertiary structure of bacterial selenocysteine tRNA
Resolution
3.095 Å
Binding residue
(original residue number in PDB)
A317 R349 E351 V361 F364 R366 E368 F409 S449 V450 G451 S452 C478 G482 R485
Binding residue
(residue number reindexed from 1)
A317 R349 E351 V361 F364 R366 E368 F409 S449 V450 G451 S452 C478 G482 R485
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
C319 R349 E351 R360 E368 E430 S449 S452 C478 R485
Catalytic site (residue number reindexed from 1)
C319 R349 E351 R360 E368 E430 S449 S452 C478 R485
Enzyme Commision number
6.1.1.11
: serine--tRNA ligase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004812
aminoacyl-tRNA ligase activity
GO:0004828
serine-tRNA ligase activity
GO:0005524
ATP binding
GO:0008270
zinc ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006412
translation
GO:0006418
tRNA aminoacylation for protein translation
GO:0006434
seryl-tRNA aminoacylation
GO:0016260
selenocysteine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3w3s
,
PDBe:3w3s
,
PDBj:3w3s
PDBsum
3w3s
PubMed
23649835
UniProt
Q8TVD2
|SYS2_METKA Type-2 serine--tRNA ligase (Gene Name=serS)
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