Structure of PDB 2hse Chain C Binding Site BS02
Receptor Information
>2hse Chain C (length=310) Species:
562
(Escherichia coli) [
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ANPLYQKHIISINDLSRDDLNLVLATAAKLKANPQPELLKHKVIASCFFE
ASTRTRLSFETSMHRLGASVVGFSDSANTSLGKKGETLADTISVISTYVD
AIVMRHPQEGAARLATEFSGNVPVLNAGDGSNQHPTQTLLDLFTIQETQG
RLDNLHVAMVGDLKYGRTVHSLTQALAKFDGNRFYFIAPDALAMPQYILD
MLDEKGIAWSLHSSIEEVMAEVDILYMTRVQKERLAPSEYANVKAQFVLR
ASDLHNAKANMKVLHPLPRVDEIATDVDKTPHAWYFQQAGNGIFARQALL
ALVLNRDLVL
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
2hse Chain C Residue 912 [
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Receptor-Ligand Complex Structure
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PDB
2hse
The allosteric transition induced by the aspartate binding to Aspartate Transcarbamoylase
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
R167 R229 Q231 L267 P268
Binding residue
(residue number reindexed from 1)
R167 R229 Q231 L267 P268
Annotation score
5
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:2hse
,
PDBe:2hse
,
PDBj:2hse
PDBsum
2hse
PubMed
UniProt
P0A786
|PYRB_ECOLI Aspartate carbamoyltransferase catalytic subunit (Gene Name=pyrB)
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