Structure of PDB 6jl4 Chain B Binding Site BS02
Receptor Information
>6jl4 Chain B (length=319) Species:
5693
(Trypanosoma cruzi) [
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SMLELPPVASLKGKSITSAEQFSRADIYALIHLASAMQRKIDAGEVLNLL
QGRIMTPLFFEDSSRTFSSFCAAMIRLGGSVVNFKVEASSINKGETLADT
IRTLDSYSDVLVMRHPRQDAIEEALSVAQHPILNAGNGAGEHPTQALLDT
LTIHSELGSVDGITIALIGDLKMGRTVHSLLKLLVRNFSIKCVFLVAPDA
LQMPQDVLEPLQHEIATKGVIIHRTHALTDEVMQKSDVLYTTRLQKDDAA
ALQSFAAKADITIDAARMRLAKEKMIVMHPLPRNDELSTTVDADPRAAYF
RQMRYGMFMRMAILWSVLA
Ligand information
Ligand ID
CP
InChI
InChI=1S/CH4NO5P/c2-1(3)7-8(4,5)6/h(H2,2,3)(H2,4,5,6)
InChIKey
FFQKYPRQEYGKAF-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)O[P](O)(O)=O
OpenEye OEToolkits 1.5.0
C(=O)(N)OP(=O)(O)O
Formula
C H4 N O5 P
Name
PHOSPHORIC ACID MONO(FORMAMIDE)ESTER
ChEMBL
CHEMBL369105
DrugBank
ZINC
ZINC000008383183
PDB chain
6jl4 Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
6jl4
Crystallographic snapshots of Trypanosoma cruzi aspartate transcarbamoylase revealed an ordered Bi-Bi reaction mechanism
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
S62 S63 R64 T65 R113 H141 Q144
Binding residue
(residue number reindexed from 1)
S63 S64 R65 T66 R114 H142 Q145
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
R113 H141 Q144 T241 P287 G313
Catalytic site (residue number reindexed from 1)
R114 H142 Q145 T242 P280 G306
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:6jl4
,
PDBe:6jl4
,
PDBj:6jl4
PDBsum
6jl4
PubMed
UniProt
O15636
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