Structure of PDB 4eei Chain A Binding Site BS01
Receptor Information
>4eei Chain A (length=414) Species:
177416
(Francisella tularensis subsp. tularensis SCHU S4) [
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MIKRYDVAEISKIWADENKYAKMLEVELAILEALEDRMVPKGTAAEIRAR
AQIRPERVDEIEKVTKHDIIAFCTSIAEQFTAETGKFFHFGVTSSDIIDS
ALSLQIRDSMSYVIKDLEALCDSLLTKAEETKEIITMGRSHGMFAEPMSF
GQKFLGAYVEFKRRLKDLKDFQKDGLTVQFSGAVGNYCILTTEDEKKAAD
ILGLPVEEVSTQVIPRDRIAKLISIHGLIASAIERLAVEIRHLHRSDVFE
VYEGFKKNPISTENLTGMARMLRSHVSIALENCVLWHERDISHSSAERFY
LPDNFGIMVYALRRMKNTIDNLVVQRDIIEDRVRSTSAYLSSFYLHFLVA
NTPFMREDCYKIVQQVESFSKKLQKVMHDEHNIILDIPEMDFEGIKKTYL
KEIDHVFDRSVKAR
Ligand information
Ligand ID
AMP
InChI
InChI=1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(22-10)1-21-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
UDMBCSSLTHHNCD-KQYNXXCUSA-N
SMILES
Software
SMILES
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(O)=O)[CH](O)[CH]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N
ACDLabs 12.01
O=P(O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)O)O)O)N
Formula
C10 H14 N5 O7 P
Name
ADENOSINE MONOPHOSPHATE
ChEMBL
CHEMBL752
DrugBank
DB00131
ZINC
ZINC000003860156
PDB chain
4eei Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
4eei
Crystal Structure of Adenylosuccinate Lyase from Francisella tularensis Complexed with AMP and Succinate
Resolution
1.921 Å
Binding residue
(original residue number in PDB)
K66 H67 D68 Q212 R301 I303 S306 R310
Binding residue
(residue number reindexed from 1)
K66 H67 D68 Q212 R289 I291 S294 R298
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H67 S140 H141 K268 E275
Catalytic site (residue number reindexed from 1)
H67 S140 H141 K256 E263
Enzyme Commision number
4.3.2.2
: adenylosuccinate lyase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003824
catalytic activity
GO:0004018
N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity
GO:0016829
lyase activity
GO:0070626
(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity
Biological Process
GO:0006164
purine nucleotide biosynthetic process
GO:0006189
'de novo' IMP biosynthetic process
GO:0009152
purine ribonucleotide biosynthetic process
GO:0044208
'de novo' AMP biosynthetic process
GO:0044281
small molecule metabolic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4eei
,
PDBe:4eei
,
PDBj:4eei
PDBsum
4eei
PubMed
UniProt
Q5NIQ1
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