Structure of PDB 1r0c Chain G Binding Site BS02
Receptor Information
>1r0c Chain G (length=310) Species:
562
(Escherichia coli) [
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ANPLYQKHIISINDLSRDDLNLVLATAAKLKANPQPELLKHKVIASCFFE
ASTRTRLSFETSMHRLGASVVGFSDSANTSLGKKGETLADTISVISTYVD
AIVMRHPQEGAARLATEFSGNVPVLNAGDGSNQHPTQTLLDLFTIQETQG
RLDNLHVAMVGDLKYGRTVHSLTQALAKFDGNRFYFIAPDALAMPQYILD
MLDEKGIAWSLHSSIEEVMAEVDILYMTRVQKERLDPSEYANVKAQFVLR
ASDLHNAKANMKVLHPLPRVDEIATDVDKTPHAWYFQQAGNGIFARQALL
ALVLNRDLVL
Ligand information
Ligand ID
NCD
InChI
InChI=1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12)/t2-/m0/s1
InChIKey
HLKXYZVTANABHZ-REOHCLBHSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)N[C@@H](CC(O)=O)C(O)=O
OpenEye OEToolkits 1.5.0
C([C@@H](C(=O)O)NC(=O)N)C(=O)O
ACDLabs 10.04
O=C(O)C(NC(=O)N)CC(=O)O
OpenEye OEToolkits 1.5.0
C(C(C(=O)O)NC(=O)N)C(=O)O
CACTVS 3.341
NC(=O)N[CH](CC(O)=O)C(O)=O
Formula
C5 H8 N2 O5
Name
N-CARBAMOYL-L-ASPARTATE
ChEMBL
DrugBank
DB04252
ZINC
ZINC000000895230
PDB chain
1r0c Chain G Residue 2002 [
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Receptor-Ligand Complex Structure
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PDB
1r0c
Products in the T-State of Aspartate Transcarbamylase: Crystal Structure of the Phosphate and N-Carbamyl-l-aspartate Ligated Enzyme
Resolution
2.37 Å
Binding residue
(original residue number in PDB)
S52 R54
Binding residue
(residue number reindexed from 1)
S52 R54
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
T228 P266 G292
Catalytic site (residue number reindexed from 1)
T228 P266 G292
Enzyme Commision number
2.1.3.2
: aspartate carbamoyltransferase.
Gene Ontology
Molecular Function
GO:0004070
aspartate carbamoyltransferase activity
GO:0004088
carbamoyl-phosphate synthase (glutamine-hydrolyzing) activity
GO:0005515
protein binding
GO:0016597
amino acid binding
GO:0016740
transferase activity
GO:0016743
carboxyl- or carbamoyltransferase activity
GO:0042802
identical protein binding
Biological Process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006221
pyrimidine nucleotide biosynthetic process
GO:0006520
amino acid metabolic process
GO:0006541
glutamine metabolic process
GO:0044205
'de novo' UMP biosynthetic process
GO:0070207
protein homotrimerization
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0009347
aspartate carbamoyltransferase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1r0c
,
PDBe:1r0c
,
PDBj:1r0c
PDBsum
1r0c
PubMed
15157076
UniProt
P0A786
|PYRB_ECOLI Aspartate carbamoyltransferase catalytic subunit (Gene Name=pyrB)
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