Structure of PDB 1hpu Chain B Binding Site BS03
Receptor Information
>1hpu Chain B (length=525) Species:
562
(Escherichia coli) [
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YEQDKTYKITVLHTNDHHGHFWRNEYGEYGLAAQKTLVDGIRKEVAAEGG
SVLLLSGGDINTGVPESDLQDAEPDFRGMNLVGYDAMAIGNHEFDNPLTV
LRQQEKWAKFPLLSANIYQKSTGERLFKPWALFKRQDLKIAVIGLTTDDT
AKIGNPEYFTDIEFRKPADEAKLVIQELQQTEKPDIIIAATHMGHYDNGE
HGSNAPGDVEMARALPAGSLAMIVGGHSQDPVCMAAENKKQVDYVPGTPC
KPDQQNGIWIVQAHEWGKYVGRADFEFRNGEMKMVNYQLIPVNLKKKVTW
EDGKSERVLYTPEIAENQQMISLLSPFQNKGKAQLEVKIGETNGRLEGDR
DKVRFVQTNMGRLILAAQMDRTGADFAVMSGGGIRDSIEAGDISYKNVLK
VQPFGNVVVYADMTGKEVIDYLTAVAQMKPDSGAYPQFANVSFVAKDGKL
NDLKIKGEPVDPAKTYRMATLNFNATGGDGYPRLDNKPGYVNTGFIDAEV
LKAYIQKSSPLDVSVYEPKGEVSWQ
Ligand information
Ligand ID
A12
InChI
InChI=1S/C11H17N5O9P2/c12-9-6-10(14-2-13-9)16(3-15-6)11-8(18)7(17)5(25-11)1-24-27(22,23)4-26(19,20)21/h2-3,5,7-8,11,17-18H,1,4H2,(H,22,23)(H2,12,13,14)(H2,19,20,21)/t5-,7-,8-,11-/m1/s1
InChIKey
OLCWZBFDIYXLAA-IOSLPCCCSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(CP(=O)(O)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)C[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)CP(=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)(CP(=O)(O)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)C[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C11 H17 N5 O9 P2
Name
PHOSPHOMETHYLPHOSPHONIC ACID ADENOSYL ESTER;
ALPHA,BETA-METHYLENEADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL583969
DrugBank
DB03148
ZINC
ZINC000013527614
PDB chain
1hpu Chain B Residue 1603 [
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Receptor-Ligand Complex Structure
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PDB
1hpu
Mechanism of hydrolysis of phosphate esters by the dimetal center of 5'-nucleotidase based on crystal structures.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
N116 H117 D120 I178 H252 R375 R379 G407 R410 F429 N431 F498 D504
Binding residue
(residue number reindexed from 1)
N91 H92 D95 I153 H227 R350 R354 G382 R385 F404 N406 F473 D479
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 R350 R354 R385
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:1hpu
,
PDBe:1hpu
,
PDBj:1hpu
PDBsum
1hpu
PubMed
11491293
UniProt
P07024
|USHA_ECOLI Protein UshA (Gene Name=ushA)
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