Structure of PDB 3eca Chain A Binding Site BS01
Receptor Information
>3eca Chain A (length=326) Species:
562
(Escherichia coli) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
LPNITILATGGTIAGGGDSATKSNYTAGKVGVENLVNAVPQLKDIANVKG
EQVVNIGSQDMNDDVWLTLAKKINTDCDKTDGFVITHGTDTMEETAYFLD
LTVKCDKPVVMVGAMRPSTSMSADGPFNLYNAVVTAADKASANRGVLVVM
NDTVLDGRDVTKTNTTDVATFKSVNYGPLGYIHNGKIDYQRTPARKHTSD
TPFDVSKLNELPKVGIVYNYANASDLPAKALVDAGYDGIVSAGVGNGNLY
KTVFDTLATAAKNGTAVVRSSRVPTGATTQDAEVDDAKYGFVASGTLNPQ
KARVLLQLALTQTKDPQQIQQIFNQY
Ligand information
Ligand ID
ASP
InChI
InChI=1S/C4H7NO4/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H,6,7)(H,8,9)/t2-/m0/s1
InChIKey
CKLJMWTZIZZHCS-REOHCLBHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(C(=O)O)N)C(=O)O
OpenEye OEToolkits 1.7.0
C([C@@H](C(=O)O)N)C(=O)O
CACTVS 3.370
N[CH](CC(O)=O)C(O)=O
CACTVS 3.370
N[C@@H](CC(O)=O)C(O)=O
ACDLabs 12.01
O=C(O)CC(N)C(=O)O
Formula
C4 H7 N O4
Name
ASPARTIC ACID
ChEMBL
CHEMBL274323
DrugBank
DB00128
ZINC
ZINC000000895032
PDB chain
3eca Chain A Residue 401 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
3eca
Crystal structure of Escherichia coli L-asparaginase, an enzyme used in cancer therapy.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
T12 G57 S58 Q59 G88 T89 D90
Binding residue
(residue number reindexed from 1)
T12 G57 S58 Q59 G88 T89 D90
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
T12 Y25 T89 D90 K162 E283
Catalytic site (residue number reindexed from 1)
T12 Y25 T89 D90 K162 E283
Enzyme Commision number
3.5.1.1
: asparaginase.
Gene Ontology
Molecular Function
GO:0004067
asparaginase activity
GO:0016787
hydrolase activity
GO:0042802
identical protein binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0006528
asparagine metabolic process
GO:0006530
asparagine catabolic process
GO:0051289
protein homotetramerization
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
GO:0032991
protein-containing complex
GO:0042597
periplasmic space
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3eca
,
PDBe:3eca
,
PDBj:3eca
PDBsum
3eca
PubMed
8434007
UniProt
P00805
|ASPG2_ECOLI L-asparaginase 2 (Gene Name=ansB)
[
Back to BioLiP
]