Structure of PDB 8i1n Chain D Binding Site BS01
Receptor Information
>8i1n Chain D (length=196) Species:
9606
(Homo sapiens) [
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HHVSRNKRGQVVGTRGGFRGCTVWLTGLSGAGKTTISFALEEYLVSHAIP
CYSLDGDNVRHGLNRNLGFSPGDREENIRRIAEVAKLFADAGLVCITSFI
SPFAKDRENARKIHESAGLPFFEIFVDAPLNICESRDVKGLYKRARAGEI
KGFTGIDSDYEKPETPERVLKTNLSTVSDCVHQVVELLQEQNIVPY
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-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)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
8i1n Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
8i1n
Redox switching mechanism of the adenosine 5'-phosphosulfate kinase domain (APSK2) of human PAPS synthase 2.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
G52 A53 G54 K55 T56 T57 R158 T194
Binding residue
(residue number reindexed from 1)
G30 A31 G32 K33 T34 T35 R136 T172
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.7.1.25
: adenylyl-sulfate kinase.
2.7.7.4
: sulfate adenylyltransferase.
Gene Ontology
Molecular Function
GO:0004020
adenylylsulfate kinase activity
GO:0005524
ATP binding
Biological Process
GO:0000103
sulfate assimilation
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Molecular Function
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Biological Process
External links
PDB
RCSB:8i1n
,
PDBe:8i1n
,
PDBj:8i1n
PDBsum
8i1n
PubMed
37207644
UniProt
O95340
|PAPS2_HUMAN Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2 (Gene Name=PAPSS2)
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