Structure of PDB 5irp Chain B Binding Site BS02
Receptor Information
>5irp Chain B (length=386) Species:
224308
(Bacillus subtilis subsp. subtilis str. 168) [
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MIKLCREVWIEVNLDAVKKNLRAIRRHIPHKSKIMAVVKANGYGHGSIEV
ARHALEHGASELAVASVEEGIVLRKAGITAPILVLGFTSLSCVKKSAAWN
ITLSAFQVDWMKEANEILEKEASANRLAIHINVDTGMGRLGVRTKEELLE
VVKALKASKFLRWTGIFTHFSTADEPDTTLTKLQHEKFISFLSFLKKQGI
ELPTVHMCNTAAAIAFPEFSADMIRLGIGLYGLYPSAYIKQLNLVKLEPA
LSLKARIAYVKTMRTEPRTVSYGATYIAEPNEVIATLPIGYADGYSRALS
NRGFVLHRGKRVPVAGRVTMDMIMVSLGENGEGKQGDEVVIYGKQKGAEI
SVDEVAEMLNTINYEVVSTLSRRIPRFYIRDGEIFK
Ligand information
Ligand ID
TRS
InChI
InChI=1S/C4H11NO3/c5-4(1-6,2-7)3-8/h6-8H,1-3,5H2/p+1
InChIKey
LENZDBCJOHFCAS-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
[NH3+]C(CO)(CO)CO
ACDLabs 10.04
OCC([NH3+])(CO)CO
OpenEye OEToolkits 1.5.0
C(C(CO)(CO)[NH3+])O
Formula
C4 H12 N O3
Name
2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL;
TRIS BUFFER
ChEMBL
DrugBank
ZINC
PDB chain
5irp Chain B Residue 404 [
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Receptor-Ligand Complex Structure
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PDB
5irp
Cold-induced aldimine bond cleavage by Tris in Bacillus subtilis alanine racemase.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
D174 P235 Y364
Binding residue
(residue number reindexed from 1)
D174 P235 Y364
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K39 R139 H169 R225 Y272 T319 D321
Catalytic site (residue number reindexed from 1)
K39 R139 H169 R225 Y272 T319 D321
Enzyme Commision number
5.1.1.1
: alanine racemase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008784
alanine racemase activity
GO:0016853
isomerase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0006522
alanine metabolic process
GO:0009252
peptidoglycan biosynthetic process
GO:0030632
D-alanine biosynthetic 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:5irp
,
PDBe:5irp
,
PDBj:5irp
PDBsum
5irp
PubMed
30977502
UniProt
P94494
|ALR2_BACSU Alanine racemase 2 (Gene Name=alr2)
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