Structure of PDB 1jg8 Chain B Binding Site BS02
Receptor Information
>1jg8 Chain B (length=343) Species:
2336
(Thermotoga maritima) [
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MIDLRSDTVTKPTEEMRKAMAQAEVGDDVYGEDPTINELERLAAETFGKE
AALFVPSGTMGNQVSIMAHTQRGDEVILEADSHIFWYEVGAMAVLSGVMP
HPVPGKNGAMDPDDVRKAIRPRNIHFPRTSLIAIENTHNRSGGRVVPLEN
IKEICTIAKEHGINVHIDGARIFNASIASGVPVKEYAGYADSVMFCLSKG
LCAPVGSVVVGDRDFIERARKARKMLGGGMRQAGVLAAAGIIALTKMVDR
LKEDHENARFLALKLKEIGYSVNPEDVKTNMVILRTDNLKVNAHGFIEAL
RNSGVLANAVSDTEIRLVTHKDVSRNDIEEALNIFEKLFRKFS
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1jg8 Chain B Residue 905 [
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Receptor-Ligand Complex Structure
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PDB
1jg8
Crystal Structure of Low-specificity Threonine Aldolase, a Key Enzyme in Glycine Biosynthesis
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
N330 E333
Binding residue
(residue number reindexed from 1)
N326 E329
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.1.2.5
: L-threonine aldolase.
Gene Ontology
Molecular Function
GO:0008732
L-allo-threonine aldolase activity
GO:0016829
lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0006545
glycine biosynthetic process
GO:0006567
threonine catabolic 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:1jg8
,
PDBe:1jg8
,
PDBj:1jg8
PDBsum
1jg8
PubMed
UniProt
Q9X266
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