Structure of PDB 3kzn Chain A Binding Site BS01
Receptor Information
>3kzn Chain A (length=332) Species:
190485
(Xanthomonas campestris pv. campestris str. ATCC 33913) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
LKHFLNTQDWSRAELDALLTQAALFKRNKLGSELKGKSIALVFFNPSMRT
RTSFELGAFQLGGHAVVLQPGKDAWPIEFNLGTVMDGDTEEHIAEVARVL
GRYVDLIGVRAFPKFVDWSKDREDQVLKSFAKYSPVPVINMETITHPCQE
LAHALALQEHFGTPDLRGKKYVLTWTYHPKPLNTAVANSALTIATRMGMD
VTLLCPTPDYILDERYMDWAAQNVAESGGSLQVSHDIDSAYAGADVVYAK
SWGALPFFGNWEPEKPIRDQYQHFIVDERKMALTNNGVFSHCLPLRRNVK
ATDAVMDSPNCIAIDEAENRLHVQKAIMAALV
Ligand information
Ligand ID
AOR
InChI
InChI=1S/C7H14N2O3/c1-5(10)9-6(7(11)12)3-2-4-8/h6H,2-4,8H2,1H3,(H,9,10)(H,11,12)/t6-/m0/s1
InChIKey
JRLGPAXAGHMNOL-LURJTMIESA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)N[C@@H](CCCN)C(=O)O
CACTVS 3.341
CC(=O)N[CH](CCCN)C(O)=O
OpenEye OEToolkits 1.5.0
CC(=O)NC(CCCN)C(=O)O
ACDLabs 10.04
O=C(NC(C(=O)O)CCCN)C
CACTVS 3.341
CC(=O)N[C@@H](CCCN)C(O)=O
Formula
C7 H14 N2 O3
Name
N~2~-ACETYL-L-ORNITHINE
ChEMBL
DrugBank
ZINC
ZINC000001532657
PDB chain
3kzn Chain A Residue 345 [
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
3kzn
Structures of N-acetylornithine transcarbamoylase from Xanthomonas campestris complexed with substrates and substrate analogs imply mechanisms for substrate binding and catalysis.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
F114 E144 L184 K252 C294 L295
Binding residue
(residue number reindexed from 1)
F112 E142 L182 K250 C292 L293
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
R112 H148 Q151 K252 C294 R322
Catalytic site (residue number reindexed from 1)
R110 H146 Q149 K250 C292 R320
Enzyme Commision number
2.1.3.9
: N-acetylornithine carbamoyltransferase.
Gene Ontology
Molecular Function
GO:0004585
ornithine carbamoyltransferase activity
GO:0016597
amino acid binding
GO:0016740
transferase activity
GO:0016743
carboxyl- or carbamoyltransferase activity
GO:0043857
N-acetylornithine carbamoyltransferase activity
Biological Process
GO:0006520
amino acid metabolic process
GO:0006526
L-arginine biosynthetic process
GO:0019240
citrulline biosynthetic process
GO:0042450
arginine biosynthetic process via ornithine
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3kzn
,
PDBe:3kzn
,
PDBj:3kzn
PDBsum
3kzn
PubMed
16741992
UniProt
Q8P8J2
|AOTC_XANCP N-acetylornithine carbamoyltransferase (Gene Name=argF')
[
Back to BioLiP
]