Structure of PDB 4o9k Chain A Binding Site BS01
Receptor Information
>4o9k Chain A (length=130) Species:
243233
(Methylococcus capsulatus str. Bath) [
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GRRLLTFVRDIMHTGDDTPVIGLEASVRDALLEMTAKKLGMTAIVDGAGT
IQGVFTDGDLRRLLEKAQDIHATPITAVMTRSCVTVEGSLLAAEAVRIME
QKRINALPVVENGRLIGAINMHDLLRAGVL
Ligand information
Ligand ID
CMK
InChI
InChI=1S/C17H26N3O15P/c18-9-1-2-20(16(29)19-9)14-12(26)11(25)8(33-14)5-32-36(30,31)35-17(15(27)28)3-6(22)10(24)13(34-17)7(23)4-21/h1-2,6-8,10-14,21-26H,3-5H2,(H,27,28)(H,30,31)(H2,18,19,29)/t6-,7-,8-,10-,11-,12-,13-,14-,17-/m1/s1
InChIKey
YWWJKULNWGRYAS-UOVSKDHASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1[C@H]([C@H]([C@H](O[C@@]1(C(=O)O)O[P@@](=O)(O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=NC3=O)N)O)O)[C@@H](CO)O)O)O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[C@]3(C[C@@H](O)[C@@H](O)[C@H](O3)[C@H](O)CO)C(O)=O)[C@@H](O)[C@H]2O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[CH]2O[CH](CO[P](O)(=O)O[C]3(C[CH](O)[CH](O)[CH](O3)[CH](O)CO)C(O)=O)[CH](O)[CH]2O
ACDLabs 10.04
O=C(O)C1(OC(C(O)CO)C(O)C(O)C1)OP(=O)(O)OCC3OC(N2C(=O)N=C(N)C=C2)C(O)C3O
OpenEye OEToolkits 1.5.0
C1C(C(C(OC1(C(=O)O)OP(=O)(O)OCC2C(C(C(O2)N3C=CC(=NC3=O)N)O)O)C(CO)O)O)O
Formula
C17 H26 N3 O15 P
Name
CYTIDINE 5'-MONOPHOSPHATE 3-DEOXY-BETA-D-GULO-OCT-2-ULO-PYRANOSONIC ACID;
CMP-2-KETO-3-DEOXY-OCTULOSONIC ACID
ChEMBL
DrugBank
DB04482
ZINC
ZINC000030725157
PDB chain
4o9k Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4o9k
Crystal structure and kinetic properties of D-arabinose 5-phosphate isomerase from Methylococcus capsulatus
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
V254 T256 D259 R262 T280 C283 V284 I304 N305 A306
Binding residue
(residue number reindexed from 1)
V54 T56 D59 R62 T80 C83 V84 I104 N105 A106
Annotation score
1
Enzymatic activity
Enzyme Commision number
5.3.1.13
: arabinose-5-phosphate isomerase.
External links
PDB
RCSB:4o9k
,
PDBe:4o9k
,
PDBj:4o9k
PDBsum
4o9k
PubMed
UniProt
Q60AU8
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