Structure of PDB 1g8m Chain A Binding Site BS01
Receptor Information
>1g8m Chain A (length=590) Species:
9031
(Gallus gallus) [
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RQQLALLSVSEKAGLVEFARSLNALGLGLIASGGTATALRDAGLPVRDVS
DLTGFPEMLGGRVKTLHPAVHAGILARNIPEDNADMNKQDFSLVRVVVCN
LYPFVKTVSSPGVTVPEAVEKIDIGGVALLRAAAKNHARVTVVCDPADYS
SVAKEMAASKDKDTSVETRRHLALKAFTHTAQYDAAISDYFRKEYSKGVS
QLPLRYGMNPHQSPAQLYTTRPKLPLTVVNGSPGFINLCDALNAWQLVKE
LKQALGIPAAASFKHVSPAGAAVGIPLSEEEAQVCMVHDLHKTLTPLASA
YARSRGADRMSSFGDFIALSDICDVPTAKIISREVSDGVVAPGYEEEALK
ILSKKKNGGYCVLQMDPNYEPDDNEIRTLYGLQLMQKRNNAVIDRSLFKN
IVTKNKTLPESAVRDLIVASIAVKYTQSNSVCYAKDGQVIGIGAGQQSRI
HCTRLAGDKANSWWLRHHPRVLSMKFKAGVKRAEVSNAIDQYVTGTIGED
EDLVKWQAMFEEVPAQLTEAEKKQWIAKLTAVSLSSDAFFPFRDNVDRAK
RIGVQFIVAPSGSAADEVVIEACNELGITLIHTNLRLFHH
Ligand information
Ligand ID
G
InChI
InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(23-9)1-22-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
RQFCJASXJCIDSX-UUOKFMHZSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=C1c2ncn(c2N=C(N)N1)C3OC(C(O)C3O)COP(=O)(O)O
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)O)O)O)N=C(NC2=O)N
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N=C(NC2=O)N
Formula
C10 H14 N5 O8 P
Name
GUANOSINE-5'-MONOPHOSPHATE
ChEMBL
CHEMBL283807
DrugBank
DB01972
ZINC
ZINC000002159505
PDB chain
1g8m Chain A Residue 2001 [
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Receptor-Ligand Complex Structure
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PDB
1g8m
Crystal structure of a bifunctional transformylase and cyclohydrolase enzyme in purine biosynthesis.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
S11 V12 S13 S35 G37 T38 R65 K67 T68 L69 N103 L104 Y105 D126 I127 G128 G129
Binding residue
(residue number reindexed from 1)
S8 V9 S10 S32 G34 T35 R62 K64 T65 L66 N100 L101 Y102 D123 I124 G125 G126
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
K267 H268 N432 H593
Catalytic site (residue number reindexed from 1)
K264 H265 N429 H590
Enzyme Commision number
2.1.2.3
: phosphoribosylaminoimidazolecarboxamide formyltransferase.
3.5.4.10
: IMP cyclohydrolase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003937
IMP cyclohydrolase activity
GO:0004643
phosphoribosylaminoimidazolecarboxamide formyltransferase activity
GO:0016740
transferase activity
GO:0016787
hydrolase activity
GO:0042803
protein homodimerization activity
Biological Process
GO:0006164
purine nucleotide biosynthetic process
GO:0006189
'de novo' IMP biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1g8m
,
PDBe:1g8m
,
PDBj:1g8m
PDBsum
1g8m
PubMed
11323713
UniProt
P31335
|PUR9_CHICK Bifunctional purine biosynthesis protein ATIC (Gene Name=ATIC)
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