Structure of PDB 3k2v Chain A Binding Site BS02
Receptor Information
>3k2v Chain A (length=130) Species:
272620
(Klebsiella pneumoniae subsp. pneumoniae MGH 78578) [
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GALGRKLLLRVNDIMHTGDEIPHVGLQATLRDALLEITRKNLGMTAICDD
DMNIIGIFTDGDLRRVFDTGVDMRDASIADVMTRGGIRIRPGTLAVDALN
LMQSRHITCVLVADGDHLLGVVHMHDLLRA
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
3k2v Chain B Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
3k2v
Structure of the CBS pair of a putative D-arabinose 5-phosphate isomerase from Klebsiella pneumoniae subsp. pneumoniae.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
N242 G244 D261 H326
Binding residue
(residue number reindexed from 1)
N41 G43 D60 H125
Annotation score
1
Enzymatic activity
Enzyme Commision number
5.3.1.13
: arabinose-5-phosphate isomerase.
External links
PDB
RCSB:3k2v
,
PDBe:3k2v
,
PDBj:3k2v
PDBsum
3k2v
PubMed
UniProt
A6TEL6
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