Structure of PDB 1r0b Chain D Binding Site BS01
Receptor Information
>1r0b Chain D (length=310) Species:
562
(Escherichia coli) [
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ANPLYQKHIISINDLSRDDLNLVLATAAKLKANPQPELLKHKVIASCFFE
ASTRTRLSFETSMHRLGASVVGFSDSANTSLGKKGETLADTISVISTYVD
AIVMRHPQEGAARLATEFSGNVPVLNAGDGSNQHPTQTLLDLFTIQETQG
RLDNLHVAMVGDLKYGRTVHSLTQALAKFDGNRFYFIAPDALAMPQYILD
MLDEKGIAWSLHSSIEEVMAEVDILYMTRVQKERLDPSEYANVKAQFVLR
ASDLHNAKANMKVLHPLPRVDEIATDVDKTPHAWYFQQAGNGIFARQALL
ALVLNRDLVL
Ligand information
Ligand ID
FLC
InChI
InChI=1S/C6H8O7/c7-3(8)1-6(13,5(11)12)2-4(9)10/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/p-3
InChIKey
KRKNYBCHXYNGOX-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
OC(CC([O-])=O)(CC([O-])=O)C([O-])=O
OpenEye OEToolkits 1.5.0
C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O
ACDLabs 10.04
O=C([O-])CC(O)(C([O-])=O)CC(=O)[O-]
Formula
C6 H5 O7
Name
CITRATE ANION
ChEMBL
DrugBank
ZINC
PDB chain
1r0b Chain D Residue 2004 [
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Receptor-Ligand Complex Structure
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PDB
1r0b
Aspartate Transcarbamylase (ATCase) of Escherichia coli: A New Crystalline R-State Bound to PALA, or to Product Analogues Citrate and Phosphate
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
T55 R105 H134 Q137 R167 T168 Q231 P266
Binding residue
(residue number reindexed from 1)
T55 R105 H134 Q137 R167 T168 Q231 P266
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R54 T55 K84 R105 H134 Q137 T228 P266 G292
Catalytic site (residue number reindexed from 1)
R54 T55 K84 R105 H134 Q137 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:1r0b
,
PDBe:1r0b
,
PDBj:1r0b
PDBsum
1r0b
PubMed
15157075
UniProt
P0A786
|PYRB_ECOLI Aspartate carbamoyltransferase catalytic subunit (Gene Name=pyrB)
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