Structure of PDB 7b2e Chain D Binding Site BS03
Receptor Information
>7b2e Chain D (length=548) Species:
272630
(Methylorubrum extorquens AM1) [
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PELTDGFHLVIDALKLNGIETIYNVPGIPITDLGRLAQAEGLRVISFRHE
QNAGNAAAIAGFLTKKPGICLTVSAPGFLNGLTALANATTNCFPMILISG
SSEREIVDLQQGDYGEMDQLAIAKPLCKAAFRVLHAADIGIGVARAIRAA
VSGRPGGVYLDLPAKLFSQVIDADLGARSLVKVIDAAPAQLPAPAAIARA
LDVLKSAERPLIILGKGAAYAQADEAVRALVEESGIPYVPMSMAKGLLPD
THPLSAGAARSTALKDSDVVLLVGARLNWLLSHGKGKTWGEPGSKRFIQI
DIEPREMDSNVEIVAPVVGDIGSCVEALLDGIRKDWKGAPSNWLETLRGK
REANIAKMAPKLMKNSSPMCFHSALGALRTVIKERPDAILVNEGCNTLDL
ARGIIDMYQPRKRLDVGTWGVMGIGMGFAVAAAVETGKPVLAVEGDSAFG
FSGMEVETICRYELPVCIVIFNNNGIFRGTDTDPTGRDPGTTVFVKNSRY
DKMMEAFGGVGVNVTTPDELKRAVDEAMNSGKPTLINAEIDPAAGSEG
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=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)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
7b2e Chain D Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
7b2e
Engineering a Highly Efficient Carboligase for Synthetic One-Carbon Metabolism.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
C112 R174 K236 G237 M261 G294 R296 D321 I322 D340 I341
Binding residue
(residue number reindexed from 1)
C92 R154 K216 G217 M241 G274 R276 D301 I302 D320 I321
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
V45 G47 I48 P49 I50 E70 V93 Y134 G135 A184 L301 G414 G440 M442 I496 R498 G499 T502
Catalytic site (residue number reindexed from 1)
V25 G27 I28 P29 I30 E50 V73 Y114 G115 A164 L281 G394 G420 M422 I476 R478 G479 T482
Enzyme Commision number
4.1.1.8
: oxalyl-CoA decarboxylase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0008949
oxalyl-CoA decarboxylase activity
GO:0016829
lyase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
Biological Process
GO:0001561
fatty acid alpha-oxidation
GO:0019752
carboxylic acid metabolic process
GO:0033611
oxalate catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:7b2e
,
PDBe:7b2e
,
PDBj:7b2e
PDBsum
7b2e
PubMed
34484855
UniProt
C5AX46
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