Structure of PDB 3hk5 Chain B Binding Site BS01
Receptor Information
>3hk5 Chain B (length=410) Species:
272558
(Halalkalibacterium halodurans C-125) [
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SREVLAEKVKNAVNNQPVTDMHTHLFSPNFGEILLWDIDELLTYHYLVAE
VMRWTDVSIEAFWAMSKREQADLIWEELFIKRSPVSEACRGVLTCLQGLG
LDPATRDLQVYREYFAKKTSEEQVDTVLQLANVSDVVMTNDPFDDNERIS
WLEGKQPDSRFHAALRLDPLLNEYEQTKHRLRDWGYKVNDEWNEGSIQEV
KRFLTDWIERMDPVYMAVSLPPTFSFPEESNRGRIIRDCLLPVAEKHNIP
FAMMIGVKKRVHPALGDAGDFVGKASMDGVEHLLREYPNNKFLVTMLSRE
NQHELVVLARKFSNLMIFGCWWFMNNPEIINEMTRMRMEMLGTSFIPQHS
DARVLEQLIYKWHHSKSIIAEVLIDKYDDILQAGWEVTEEEIKRDVADLF
SRNFWRFVGR
Ligand information
Ligand ID
RAT
InChI
InChI=1S/C5H8O7/c6-1(2(7)4(9)10)3(8)5(11)12/h1-3,6-8H,(H,9,10)(H,11,12)/t2-,3-/m0/s1
InChIKey
NPTTZSYLTYJCPR-HRFVKAFMSA-N
SMILES
Software
SMILES
CACTVS 3.341
O[C@@H]([C@H](O)C(O)=O)[C@H](O)C(O)=O
OpenEye OEToolkits 1.5.0
C([C@@H](C(=O)O)O)([C@@H](C(=O)O)O)O
CACTVS 3.341
O[CH]([CH](O)C(O)=O)[CH](O)C(O)=O
ACDLabs 10.04
O=C(O)C(O)C(O)C(O)C(=O)O
OpenEye OEToolkits 1.5.0
C(C(C(=O)O)O)(C(C(=O)O)O)O
Formula
C5 H8 O7
Name
D-arabinaric acid;
D-arabinarate
ChEMBL
DrugBank
ZINC
ZINC000001564966
PDB chain
3hk5 Chain B Residue 428 [
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Receptor-Ligand Complex Structure
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PDB
3hk5
The mechanism of the reaction catalyzed by uronate isomerase illustrates how an isomerase may have evolved from a hydrolase within the amidohydrolase superfamily.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
H28 H49 Y50 R170 M258 W325 W326 D355 R357
Binding residue
(residue number reindexed from 1)
H24 H45 Y46 R166 M254 W321 W322 D351 R353
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:3hk5
,
PDBe:3hk5
,
PDBj:3hk5
PDBsum
3hk5
PubMed
19678710
UniProt
Q9KFI6
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