Structure of PDB 1ahx Chain A Binding Site BS02
Receptor Information
>1ahx Chain A (length=396) Species:
562
(Escherichia coli) [
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MFENITAAPADPILGLADLFRADERPGKINLGIGLYYDETGKIPVLTSVK
KAEQYLLENETTKLYLGIDGIPEFGRCTQELLFGKGSALINDKRARTAQT
PGGSGALRVAADFLAKNTSVKRVWVSNPSWPNHKSVFNSAGLEVREYAYY
DAENHTLDFDALINSLNEAQAGDVVLFHGCCHNPTGIDPTLEQWQTLAQL
SVEKGWLPLFDFAYQGFARGLEEDAEGLRAFAAMHKELIVASSYSKNFGL
YNERVGACTLVAADSETVDRAFSQMKAAIRANYSSPPAHGASVVATILSN
DALRAIWEQELTDMRQRIQRMRQLFVNTLQEKGANRDFSFIIKQNGMFSF
SGLTKEQVLRLREEFGVYAVASGRVNVAGMTPDNMAPLCEAIVAVL
Ligand information
Ligand ID
HCI
InChI
InChI=1S/C9H10O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)
InChIKey
XMIIGOLPHOKFCH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)CCc1ccccc1
OpenEye OEToolkits 1.7.6
c1ccc(cc1)CCC(=O)O
CACTVS 3.370
OC(=O)CCc1ccccc1
Formula
C9 H10 O2
Name
HYDROCINNAMIC ACID;
3PP;
3-PHENYLPROPIONIC ACID
ChEMBL
CHEMBL851
DrugBank
DB02024
ZINC
ZINC000000154564
PDB chain
1ahx Chain A Residue 411 [
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Receptor-Ligand Complex Structure
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PDB
1ahx
Alternating arginine-modulated substrate specificity in an engineered tyrosine aminotransferase.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
I17 L18 G38 W140 K258 R386
Binding residue
(residue number reindexed from 1)
I13 L14 G34 W130 K246 R374
Annotation score
1
Binding affinity
MOAD
: Kd=120uM
PDBbind-CN
: -logKd/Ki=3.92,Kd=120uM
Enzymatic activity
Catalytic site (original residue number in PDB)
W140 D222 A224 K258
Catalytic site (residue number reindexed from 1)
W130 D211 A213 K246
Enzyme Commision number
2.6.1.1
: aspartate transaminase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004069
L-aspartate:2-oxoglutarate aminotransferase activity
GO:0004838
L-tyrosine-2-oxoglutarate transaminase activity
GO:0008483
transaminase activity
GO:0030170
pyridoxal phosphate binding
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
Biological Process
GO:0006520
amino acid metabolic process
GO:0009058
biosynthetic process
GO:0009094
L-phenylalanine biosynthetic process
GO:0033585
L-phenylalanine biosynthetic process from chorismate via phenylpyruvate
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1ahx
,
PDBe:1ahx
,
PDBj:1ahx
PDBsum
1ahx
PubMed
7664122
UniProt
P00509
|AAT_ECOLI Aspartate aminotransferase (Gene Name=aspC)
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