Structure of PDB 1tkk Chain E Binding Site BS03
Receptor Information
>1tkk Chain E (length=359) Species:
1423
(Bacillus subtilis) [
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MKIIRIETSRIAVPLTKPFKTALRTVYTAESVIVRITYDSGAVGWGEAPP
TLVITGDSMDSIESAIHHVLKPALLGKSLAGYEAILHDIQHLLTGNMSAK
AAVEMALYDGWAQMCGLPLYQMLGGYRDTLETDYTVSVNSPEEMAADAEN
YLKQGFQTLKIKVGKDDIATDIARIQEIRKRVGSAVKLRLDANQGWRPKE
AVTAIRKMEDAGLGIELVEQPVHKDDLAGLKKVTDATDTPIMADESVFTP
RQAFEVLQTRSADLINIKLMKAGGISGAEKINAMAEACGVECMVGSMIET
KLGITAAAHFAASKRNITRFDFDAPLMLKTDVFNGGITYSGSTISMPGKP
GLGIIGAAL
Ligand information
Ligand ID
GLU
InChI
InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1
InChIKey
WHUUTDBJXJRKMK-VKHMYHEASA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)C(N)CCC(=O)O
OpenEye OEToolkits 1.7.0
C(CC(=O)O)C(C(=O)O)N
OpenEye OEToolkits 1.7.0
C(CC(=O)O)[C@@H](C(=O)O)N
CACTVS 3.370
N[C@@H](CCC(O)=O)C(O)=O
CACTVS 3.370
N[CH](CCC(O)=O)C(O)=O
Formula
C5 H9 N O4
Name
GLUTAMIC ACID
ChEMBL
CHEMBL575060
DrugBank
DB00142
ZINC
ZINC000001482113
PDB chain
1tkk Chain E Residue 2479 [
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Receptor-Ligand Complex Structure
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PDB
1tkk
Evolution of Enzymatic Activities in the Enolase Superfamily: Structure of a Substrate-Liganded Complex of the l-Ala-d/l-Glu Epimerase from Bacillus subtilis(,).
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
F19 R24 K268 S296 M297 I298
Binding residue
(residue number reindexed from 1)
F19 R24 K268 S296 M297 I298
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
F19 P50 V53 T135 K160 K162 L190 D191 A192 N193 E219 D244 E245 S246 N266 K268 G295 S296 M297 F320 D321 F322
Catalytic site (residue number reindexed from 1)
F19 P50 V53 T135 K160 K162 L190 D191 A192 N193 E219 D244 E245 S246 N266 K268 G295 S296 M297 F320 D321 F322
Enzyme Commision number
5.1.1.20
: L-Ala-D/L-Glu epimerase.
Gene Ontology
Molecular Function
GO:0016853
isomerase activity
GO:0016854
racemase and epimerase activity
GO:0016855
racemase and epimerase activity, acting on amino acids and derivatives
GO:0046872
metal ion binding
GO:0103031
L-Ala-D/L-Glu epimerase activity
Biological Process
GO:0016998
cell wall macromolecule catabolic process
GO:0071555
cell wall organization
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Molecular Function
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Biological Process
External links
PDB
RCSB:1tkk
,
PDBe:1tkk
,
PDBj:1tkk
PDBsum
1tkk
PubMed
15301535
UniProt
O34508
|AEEP_BACSU L-Ala-D/L-Glu epimerase (Gene Name=ykfB)
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