Structure of PDB 1z7e Chain F Binding Site BS01
Receptor Information
>1z7e Chain F (length=639) Species:
562
(Escherichia coli) [
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MKTVVFAYHDMGCLGIEALLAAGYEISAIFTHTDGSVARLAAERGIPVYA
PDNVNHPLWVERIAQLSPDVIFSFYYRHLIYDEILQLAPAGAFNLHGSLL
PKYRGRAPLNWVLVNGETETGVTLHRMVKRADAGAIVAQLRIAIAPDDIA
ITLHHKLCHAARQLLEQTLPAIKHGNILEIAQRENEATCFGRRTPDDSFL
EWHKPASVLHNMVRAVADPWPGAFSYVGNQKFTVWSSRVHPHASKAQPGS
VISVAPLLIACGDGALEIVTGQAGDGITMQGSQLAQTLGLVQGSRLRRTR
VLILGVNGFIGNHLTERLLREDHYEVYGLDIGSDAISRFLNHPHFHFVEG
DISIHSEWIEYHVKKCDVVLPLVAIATPIEYTRNPLRVFELDFEENLRII
RYCVKYRKRIIFPSTSEVYGMCSDKYFDEDHSNLIVGPVNKPRWIYSVSK
QLLDRVIWAYGEKEGLQFTLFRPFNWMGPRLDNLNAARIGSSRAITQLIL
NLVEGSPIKLIDGGKQKRCFTDIRDGIEALYRIIENAGNRCDGEIINIGN
PENEASIEELGEMLLASFEKHPLRHHFPPFAGFRVVESSSYYGKGYQDVE
HRKPSIRNAHRCLDWEPKIDMQETIDETLDFFLRTVDLT
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
1z7e Chain F Residue 1006 [
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Receptor-Ligand Complex Structure
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PDB
1z7e
Structure and Mechanism of ArnA: Conformational Change Implies Ordered Dehydrogenase Mechanism in Key Enzyme for Polymyxin Resistance
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
G325 F326 I327 D347 I348 D368 I369 V390 R510
Binding residue
(residue number reindexed from 1)
G308 F309 I310 D330 I331 D351 I352 V373 R493
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
H104 D140
Catalytic site (residue number reindexed from 1)
H96 D132
Enzyme Commision number
1.1.1.305
: UDP-glucuronic acid oxidase (UDP-4-keto-hexauronic acid decarboxylating).
2.1.2.13
: UDP-4-amino-4-deoxy-L-arabinose formyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0016740
transferase activity
GO:0016742
hydroxymethyl-, formyl- and related transferase activity
GO:0016831
carboxy-lyase activity
GO:0042802
identical protein binding
GO:0048040
UDP-glucuronate decarboxylase activity
GO:0070403
NAD+ binding
GO:0099618
UDP-glucuronic acid dehydrogenase activity
GO:0099619
UDP-4-amino-4-deoxy-L-arabinose formyltransferase activity
Biological Process
GO:0009058
biosynthetic process
GO:0009103
lipopolysaccharide biosynthetic process
GO:0009245
lipid A biosynthetic process
GO:0033320
UDP-D-xylose biosynthetic process
GO:0046493
lipid A metabolic process
GO:0046677
response to antibiotic
GO:2001315
UDP-4-deoxy-4-formamido-beta-L-arabinopyranose biosynthetic process
Cellular Component
GO:0032991
protein-containing complex
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Cellular Component
External links
PDB
RCSB:1z7e
,
PDBe:1z7e
,
PDBj:1z7e
PDBsum
1z7e
PubMed
15939024
UniProt
P77398
|ARNA_ECOLI Bifunctional polymyxin resistance protein ArnA (Gene Name=arnA)
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