Structure of PDB 1hoo Chain A Binding Site BS01
Receptor Information
>1hoo Chain A (length=431) Species:
562
(Escherichia coli) [
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GNNVVVLGTQWGDEGKGKIVDLLTERAKYVVRYQGGHNAGHTLVINGEKT
VLHLIPSGILRENVTSIIGNGVVLSPAALMKEMKELEDRGIPVRERLLLS
EACPLILDYHVALDNAREKARGAKAIGTTGRGIGPAYEDKVARRGLRVGD
LFDKETFAEKLKEVMEYHNFQLVNYYKAEAVDYQKVLDDTMAVADILTSM
VVDVSDLLDQARQRGDFVMFEGAQGTLLDIDHGTYPYVTSSNTTAGGVAT
GSGLGPRYVDYVLGILKAYSTRVGAGPFPTELFDETGEFLCKQGNEFGAT
TGRRRRTGWLDTVAVRRAVQLNSLSGFCLTKLDVLDGLKEVKLCVAYRMP
DGREVTTTPLAADDWKGVEPIYETMPGWSESTFGVKDRSGLPQAALNYIK
RIEELTGVPIDIISTGPDRTETMILRDPFDA
Ligand information
Ligand ID
GNH
InChI
InChI=1S/C10H16N6O10P2/c11-10-14-7-4(8(19)15-10)13-2-16(7)9-6(18)5(17)3(25-9)1-24-28(22,23)26-27(12,20)21/h2-3,5-6,9,17-18H,1H2,(H,22,23)(H3,12,20,21)(H3,11,14,15,19)/t3-,5-,6-,9-/m1/s1
InChIKey
ZGPDMUBRWRJAQQ-UUOKFMHZSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](N)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](N)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(N)O)O)O)N=C(NC2=O)N
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(N)O)O)O)N=C(NC2=O)N
Formula
C10 H16 N6 O10 P2
Name
AMINOPHOSPHONIC ACID-GUANYLATE ESTER
ChEMBL
DrugBank
DB02623
ZINC
PDB chain
1hoo Chain A Residue 432A [
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Receptor-Ligand Complex Structure
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PDB
1hoo
Refined crystal structures of guanine nucleotide complexes of adenylosuccinate synthetase from Escherichia coli.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
G15 G17 G40 T300 K331 D333 S414 G416 P417
Binding residue
(residue number reindexed from 1)
G15 G17 G40 T300 K331 D333 S414 G416 P417
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
D13 K16 G40 H41 Q224
Catalytic site (residue number reindexed from 1)
D13 K16 G40 H41 Q224
Enzyme Commision number
6.3.4.4
: adenylosuccinate synthase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0000287
magnesium ion binding
GO:0004019
adenylosuccinate synthase activity
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0016874
ligase activity
GO:0046872
metal ion binding
GO:0097216
guanosine tetraphosphate binding
Biological Process
GO:0006164
purine nucleotide biosynthetic process
GO:0006974
DNA damage response
GO:0015949
nucleobase-containing small molecule interconversion
GO:0044208
'de novo' AMP biosynthetic process
GO:0046040
IMP metabolic process
GO:0046086
adenosine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1hoo
,
PDBe:1hoo
,
PDBj:1hoo
PDBsum
1hoo
PubMed
8663109
UniProt
P0A7D4
|PURA_ECOLI Adenylosuccinate synthetase (Gene Name=purA)
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