Structure of PDB 1za2 Chain C Binding Site BS01
Receptor Information
>1za2 Chain C (length=310) Species:
562
(Escherichia coli) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
ANPLYQKHIISINDLSRDDLNLVLATAAKLKANPQPELLKHKVIASCFFE
ASTRTRLSFETSMHRLGASVVGFSDSANTSLGKKGETLADTISVISTYVD
AIVMRHPQEGAARLATEFSGNVPVLNAGDGSNQHPTQTLLDLFTIQETQG
RLDNLHVAMVGDLKYGRTVHSLTQALAKFDGNRFYFIAPDALAMPQYILD
MLDEKGIAWSLHSSIEEVMAEVDILYMTRVQKERLDPSEYANVKAQFVLR
ASDLHNAKANMKVLHPLPRVDEIATDVDKTPHAWYFQQAGNGIFARQALL
ALVLNRDLVL
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
1za2 Chain C Residue 311 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1za2
Structural basis for ordered substrate binding and cooperativity in aspartate transcarbamoylase
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
S52 T53 R54 T55 R105
Binding residue
(residue number reindexed from 1)
S52 T53 R54 T55 R105
Annotation score
2
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
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1za2
,
PDBe:1za2
,
PDBj:1za2
PDBsum
1za2
PubMed
15951418
UniProt
P0A786
|PYRB_ECOLI Aspartate carbamoyltransferase catalytic subunit (Gene Name=pyrB)
[
Back to BioLiP
]