Structure of PDB 6jl5 Chain A Binding Site BS01
Receptor Information
>6jl5 Chain A (length=317) Species:
5693
(Trypanosoma cruzi) [
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GSMLELPPVASLKGKSITSAEQFSRADIYALIHLASAMQRKIDAGEVLNL
LQGRIMTPLFFEDSSRTFSSFCAAMIRLGGSVVNFKVEASSINKGETLAD
TIRTLDSYSDVLVMRHPRQDAIEEALSVAQHPILNAGNGAGEHPTQALLD
TLTIHSELGSVDGITIALIGDLKMGRTVHSLLKLLVRNFSIKCVFLVAPD
ALQMPQDVLEPLQHEIATKGVIIHRTHALTDEVMQKSDVLYTTRLQAAAL
QSFAAKADITIDAARMRLAKEKMIVMHPLPRNDELSTTVDADPRAAYFRQ
MRYGMFMRMAILWSVLA
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
6jl5 Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6jl5
Crystallographic snapshots of Trypanosoma cruzi aspartate transcarbamoylase revealed an ordered Bi-Bi reaction mechanism
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
R113 R174 R242 L288 P289
Binding residue
(residue number reindexed from 1)
R115 R176 R244 L279 P280
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
R113 H141 Q144 T241 P287 G313
Catalytic site (residue number reindexed from 1)
R115 H143 Q146 T243 P278 G304
Enzyme Commision number
2.1.3.2
: aspartate carbamoyltransferase.
Gene Ontology
Molecular Function
GO:0004070
aspartate carbamoyltransferase activity
GO:0016597
amino acid binding
GO:0016740
transferase activity
GO:0016743
carboxyl- or carbamoyltransferase activity
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0006520
amino acid metabolic process
GO:0044205
'de novo' UMP biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:6jl5
,
PDBe:6jl5
,
PDBj:6jl5
PDBsum
6jl5
PubMed
UniProt
O15636
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