Structure of PDB 4xz9 Chain B Binding Site BS02
Receptor Information
>4xz9 Chain B (length=217) Species:
273075
(Thermoplasma acidophilum DSM 1728) [
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MKIFLDTANIDEIRTGVNWGIVDGVTTNPTLISKEAVNGKKYGDIIREIL
KIVDGPVSVQVVSTKYEGMVEEARKIHGLGDNAVVKIPMTEDGLRAIKTL
SSEHINTNCTLVFNPIQALLAAKAGVTYVSPYVGRLDDIGEDGMQIIDMI
RTIFNNYIIKTQILVASIRNPIHVLRSAVIGADVVTVPFNVLKSLMKHPK
TDEGLAKFLEDWKKVSP
Ligand information
Ligand ID
G3P
InChI
InChI=1S/C3H9O6P/c4-1-3(5)2-9-10(6,7)8/h3-5H,1-2H2,(H2,6,7,8)/t3-/m1/s1
InChIKey
AWUCVROLDVIAJX-GSVOUGTGSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
C(C(COP(=O)(O)O)O)O
CACTVS 3.385
OC[C@@H](O)CO[P](O)(O)=O
ACDLabs 12.01
O=P(OCC(O)CO)(O)O
OpenEye OEToolkits 1.7.6
C([C@H](COP(=O)(O)O)O)O
CACTVS 3.385
OC[CH](O)CO[P](O)(O)=O
Formula
C3 H9 O6 P
Name
SN-GLYCEROL-3-PHOSPHATE
ChEMBL
CHEMBL1232920
DrugBank
DB02515
ZINC
ZINC000003830896
PDB chain
4xz9 Chain B Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
4xz9
Converting Transaldolase into Aldolase through Swapping of the Multifunctional Acid-Base Catalyst: Common and Divergent Catalytic Principles in F6P Aldolase and Transaldolase.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
D6 R135 S167 R169
Binding residue
(residue number reindexed from 1)
D6 R135 S167 R169
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
D6 Q60 K86 T110 Y132
Catalytic site (residue number reindexed from 1)
D6 Q60 K86 T110 Y132
Enzyme Commision number
2.2.1.2
: transaldolase.
Gene Ontology
Molecular Function
GO:0004801
transaldolase activity
GO:0016740
transferase activity
GO:0016832
aldehyde-lyase activity
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006098
pentose-phosphate shunt
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4xz9
,
PDBe:4xz9
,
PDBj:4xz9
PDBsum
4xz9
PubMed
26131847
UniProt
Q9HKI3
|TAL_THEAC Probable transaldolase (Gene Name=tal)
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