Structure of PDB 6veb Chain A Binding Site BS02
Receptor Information
>6veb Chain A (length=451) Species:
59201
(Salmonella enterica subsp. enterica) [
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MDHLPIFCQLRDRDCLIVGGGDVAERKARLLLEAGARLTVNALTFIPQFT
VWANEGMLTLVEGPFDETLLDSCWLAIAATDDDTVNQRVSDAAESRRIFC
NVVDAPKAASFIMPSIIDRSPLMVAVSAGGTSPVLARLLREKLESLLPQH
LGQVARYAGQLRARVKKQFATMGERRRFWEKFFVNDRLAQSLANADEKAV
NATTERLFSEPLDHRGEVVLVGAGPGDAGLLTLKGLQQIQQADIVVYDRL
VSDDIMNLVRRDADRVFVGKVPQEEINQILLREAQKGKRVVRLKGGDPFI
FGRGGEELETLCHAGIPFSVVPGITAASGCSAYSGIPLTHRDYAQSVRLV
TGHLKTGGELDWENLAAEKQTLVFYMGLNQAATIQEKLIAFGMQADMPVA
LVENGTSVKQRVVHGVLTQLGELAQQVESPALIIVGRVVALRDKLNWFSN
H
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
6veb Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6veb
Siroheme synthase orients substrates for dehydrogenase and chelatase activities in a common active site.
Resolution
2.55 Å
Binding residue
(original residue number in PDB)
G20 G21 D22 V23 A42 L43 T44 T80 D81 V85
Binding residue
(residue number reindexed from 1)
G20 G21 D22 V23 A42 L43 T44 T80 D81 V85
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.3.1.76
: precorrin-2 dehydrogenase.
2.1.1.107
: uroporphyrinogen-III C-methyltransferase.
4.99.1.4
: sirohydrochlorin ferrochelatase.
Gene Ontology
Molecular Function
GO:0004325
ferrochelatase activity
GO:0004851
uroporphyrin-III C-methyltransferase activity
GO:0008168
methyltransferase activity
GO:0016491
oxidoreductase activity
GO:0016829
lyase activity
GO:0043115
precorrin-2 dehydrogenase activity
GO:0051266
sirohydrochlorin ferrochelatase activity
GO:0051287
NAD binding
Biological Process
GO:0006779
porphyrin-containing compound biosynthetic process
GO:0009236
cobalamin biosynthetic process
GO:0019354
siroheme biosynthetic process
GO:0032259
methylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6veb
,
PDBe:6veb
,
PDBj:6veb
PDBsum
6veb
PubMed
32054833
UniProt
P25924
|CYSG_SALTY Siroheme synthase (Gene Name=cysG)
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