Structure of PDB 4pb4 Chain B Binding Site BS01
Receptor Information
>4pb4 Chain B (length=389) Species:
518882
(Delftia sp. HT23) [
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HHHHHHAMSMQDTLLTLDTPAAVIDLDRMQRNIARMQQRMDAQGVRLRPH
VKTSKSVPVAAAQRAAGASGITVSTLKEAEQFFAAGTTDILYAVSMAPHR
LPQALQLRRRGCDLKLIVDSVAAAQAIAAFGREQGEAFEVWIEIDTDGHR
SGVGADDTPLLLAIGRTLHDGGMRLGGVLTHAGSSYELDTPEALQALAER
ERAGCVQAAEALRAAGLPCPVVSVGSTPTALAASRLDGVTEVRAGVYVFF
DLVMRNIGVCAAEDVALSVLATVIGHQADKGWAIVDAGWMAMSRDRGTAR
QKQDFGYGQVCDLQGRVMPGFVLTGANQEHGILARADGAAEADIATRFPL
GTRLRILPNAACATGAQFPAYQALAADGSVQTWERLHGW
Ligand information
Ligand ID
2KZ
InChI
InChI=1S/C4H5NO4/c5-2(4(8)9)1-3(6)7/h1H,5H2,(H,6,7)(H,8,9)/b2-1+
InChIKey
ABZHGLSYGDUSDL-OWOJBTEDSA-N
SMILES
Software
SMILES
CACTVS 3.385
N/C(=C/C(O)=O)C(O)=O
ACDLabs 12.01
O=C(O)\C=C(\N)C(=O)O
OpenEye OEToolkits 1.9.2
C(=C(\C(=O)O)/N)\C(=O)O
OpenEye OEToolkits 1.9.2
C(=C(C(=O)O)N)C(=O)O
CACTVS 3.385
NC(=CC(O)=O)C(O)=O
Formula
C4 H5 N O4
Name
2-amino maleic acid;
(2E)-2-aminobut-2-enedioic acid
ChEMBL
DrugBank
ZINC
ZINC000167586219
PDB chain
4pb4 Chain A Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
4pb4
Structural insights into the substrate stereospecificity of D-threo-3-hydroxyaspartate dehydratase from Delftia sp. HT23: a useful enzyme for the synthesis of optically pure L-threo- and D-erythro-3-hydroxyaspartate.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
N318 Q319
Binding residue
(residue number reindexed from 1)
N327 Q328
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.3.1.27
: threo-3-hydroxy-D-aspartate ammonia-lyase.
Gene Ontology
Molecular Function
GO:0008721
D-serine ammonia-lyase activity
GO:0016829
lyase activity
GO:0016841
ammonia-lyase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0036088
D-serine catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:4pb4
,
PDBe:4pb4
,
PDBj:4pb4
PDBsum
4pb4
PubMed
25715785
UniProt
B2DFG5
|DTHAD_DELSH D-threo-3-hydroxyaspartate dehydratase (Gene Name=dthadh)
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