Structure of PDB 1xnj Chain A Binding Site BS01
Receptor Information
>1xnj Chain A (length=562) Species:
9606
(Homo sapiens) [
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HVSRNKRGQVVGTRGGFRGCTVWLTGLSGAGKTTVSMALEEYLVCHGIPC
YTLDGDNIRQGLNKNLGFSPEDREENVRRIAEVAKLFADAGLVCITSFIS
PYTQDRNNARQIHEGASLPFFEVFVDAPEYEKPEAPELVLKTDSCDVNDC
VQQVVELLQERDIVPVDASYEVKELYVPENKLHLAKTDAETLPALKINKV
DMQWVQVLAEGWATPLNGFMREREYLQCLHFDCLLDGGVINLSVPIVLTA
THEDKERLDGCTAFALMYEGRRVAILRNPEFFEHRKEERCARQWGTTCKN
HPYIKMVMEQGDWLIGGDLQVLDRVYWNDGLDQYRLTPTELKQKFKDMNA
DAVSAFQLRNPVHNGHALLMQDTHKQLLERGYRRPVLLLHPLGGWTKDDD
VPLMWRMKQHAAVLEEGVLNPETTVVAIFPSPMMYAGPTEVQWHCRARMV
AGANFYIVGRDPAGMPHPETGKDLYEPSHGAKVLTMAPGLITLEIVPFRV
AAYNKKKKRMDYYDSEHHEDFEFISGTRMRKLAREGQKPPEGFMAPKAWT
VLTEYYKSLEKA
Ligand information
Ligand ID
ADX
InChI
InChI=1S/C10H14N5O10PS/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-26(18,19)25-27(20,21)22/h2-4,6-7,10,16-17H,1H2,(H,18,19)(H2,11,12,13)(H,20,21,22)/t4-,6-,7-,10-/m1/s1
InChIKey
IRLPACMLTUPBCL-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)OS(=O)(=O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[S](O)(=O)=O)[CH](O)[CH]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OS(=O)(=O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[S](O)(=O)=O)[C@@H](O)[C@H]3O
ACDLabs 10.04
O=S(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C10 H14 N5 O10 P S
Name
ADENOSINE-5'-PHOSPHOSULFATE
ChEMBL
CHEMBL572546
DrugBank
DB03708
ZINC
ZINC000004228246
PDB chain
1xnj Chain A Residue 2900 [
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Receptor-Ligand Complex Structure
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PDB
1xnj
The crystal structure of human PAPS synthetase 1 reveals asymmetry in substrate binding
Resolution
1.98 Å
Binding residue
(original residue number in PDB)
F418 Q419 L420 R421 N422 H428 G521 R522 P524 A525 V562 A563
Binding residue
(residue number reindexed from 1)
F356 Q357 L358 R359 N360 H366 G459 R460 P462 A463 V500 A501
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
L420 R421 H425 H428 R522
Catalytic site (residue number reindexed from 1)
L358 R359 H363 H366 R460
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:0004781
sulfate adenylyltransferase (ATP) activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016779
nucleotidyltransferase activity
GO:0042803
protein homodimerization activity
Biological Process
GO:0000103
sulfate assimilation
GO:0001501
skeletal system development
GO:0006790
sulfur compound metabolic process
GO:0009152
purine ribonucleotide biosynthetic process
GO:0016310
phosphorylation
GO:0034030
ribonucleoside bisphosphate biosynthetic process
GO:0034033
purine nucleoside bisphosphate biosynthetic process
GO:0050428
3'-phosphoadenosine 5'-phosphosulfate biosynthetic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1xnj
,
PDBe:1xnj
,
PDBj:1xnj
PDBsum
1xnj
PubMed
15755455
UniProt
O43252
|PAPS1_HUMAN Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1 (Gene Name=PAPSS1)
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