Structure of PDB 1hp1 Chain A Binding Site BS04
Receptor Information
>1hp1 Chain A (length=516) Species:
562
(Escherichia coli) [
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YEQDKTYKITVLHTNDHHGHFWRNEYGEYGLAAQKTLVDGIRKEVAAEGG
SVLLLSGGDINTGVPESDLQDAEPDFRGMNLVGYDAMAIGNHEFDNPLTV
LRQQEKWAKFPLLSANIYQKSTGERLFKPWALFKRQDLKIAVIGLTTDDT
AKIGNPEYFTDIEFRKPADEAKLVIQELQQTEKPDIIIAATHMGHYDNGE
HGSNAPGDVEMARALPAGSLAMIVGGHSQDPVCMAAENKKQVDYVPGTPC
KPDQQNGIWIVQAHEWGKYVGRADFEFRNGEMKMVNYQLIPVNLKKKRVL
YTPEIAENQQMISLLSPFQNKGKAQLEVKIGETNGRLEGDRDKVRFVQTN
MGRLILAAQMDRTGADFAVMSGGGIRDSIEAGDISYKNVLKVQPFGNVVV
YADMTGKEVIDYLTAVAQMKPDSGAYPQFANVSFVAKDGKLNDLKIKGEP
VDPAKTYRMATLNFNATGGDGYPRLDNKPGYVNTGFIDAEVLKAYIQKSS
PLDVSVYEPKGEVSWQ
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=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[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
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)OP(=O)(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)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
1hp1 Chain A Residue 606 [
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Receptor-Ligand Complex Structure
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PDB
1hp1
Mechanism of hydrolysis of phosphate esters by the dimetal center of 5'-nucleotidase based on crystal structures.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
R375 R379 G407 R410 F429 N431 G458 F498 D504
Binding residue
(residue number reindexed from 1)
R341 R345 G373 R376 F395 N397 G424 F464 D470
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D41 H43 D84 N116 H117 D120 H217 H252 Q254 R375 R379 R410
Catalytic site (residue number reindexed from 1)
D16 H18 D59 N91 H92 D95 H192 H227 Q229 R341 R345 R376
Enzyme Commision number
3.1.3.5
: 5'-nucleotidase.
3.6.1.45
: UDP-sugar diphosphatase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008252
nucleotidase activity
GO:0008253
5'-nucleotidase activity
GO:0008768
UDP-sugar diphosphatase activity
GO:0016787
hydrolase activity
GO:0016788
hydrolase activity, acting on ester bonds
GO:0046872
metal ion binding
GO:0106411
XMP 5'-nucleosidase activity
Biological Process
GO:0009166
nucleotide catabolic process
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1hp1
,
PDBe:1hp1
,
PDBj:1hp1
PDBsum
1hp1
PubMed
11491293
UniProt
P07024
|USHA_ECOLI Protein UshA (Gene Name=ushA)
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