Structure of PDB 3x2f Chain A Binding Site BS01
Receptor Information
>3x2f Chain A (length=406) Species:
243274
(Thermotoga maritima MSB8) [
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NTGEMKINWVSRYMPLLNKIAEEYSREKPLSGFTVGMSIHLEAKTAYLAI
TLSKLGAKVVITGSNPLSTQDDVAEALRSKGITVYARRTHDESIYRENLM
KVLDERPDFIIDDGGDLTVISHTEREEVLENLKGVSEETTTGVRRLKALE
ETGKLRVPVIAVNDSKMKYLFDNRYGTGQSTWDAIMRNTNLLVAGKNVVV
AGYGWCGRGIALRAAGLGARVIVTEVDPVKAVEAIMDGFTVMPMKEAVKI
ADFVITASGNTDVLSKEDILSLKDGAVLANAGHFNVEIPVRVLEEIAVEK
FEARPNVTGYTLENGKTVFLLAEGRLVNLAAGDGHPVEIMDLSFALQIFA
VLYLLENHRKMSPKVYMLPDEIDERVARMKLDSLGVKIDELTEKQRRYLR
SWQHHH
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/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/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
3x2f Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3x2f
Crystal structures of S-adenosylhomocysteine hydrolase from the thermophilic bacterium Thermotoga maritima.
Resolution
2.04 Å
Binding residue
(original residue number in PDB)
T142 T143 D174 T179 G204 G206 W207 C208 T226 E227 V228 S260 G261 N262 A283 H285 N330 H337
Binding residue
(residue number reindexed from 1)
T140 T141 D172 T177 G202 G204 W205 C206 T224 E225 V226 S258 G259 N260 A281 H283 N328 H335
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
H42 G65 S70 D115 E140 N165 K170 D174 N175 T179 H285 H337 S345 Q349
Catalytic site (residue number reindexed from 1)
H40 G63 S68 D113 E138 N163 K168 D172 N173 T177 H283 H335 S343 Q347
Enzyme Commision number
3.13.2.1
: adenosylhomocysteinase.
Gene Ontology
Molecular Function
GO:0004013
adenosylhomocysteinase activity
GO:0016787
hydrolase activity
Biological Process
GO:0006730
one-carbon metabolic process
GO:0033353
S-adenosylmethionine cycle
GO:0071269
L-homocysteine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3x2f
,
PDBe:3x2f
,
PDBj:3x2f
PDBsum
3x2f
PubMed
25791616
UniProt
O51933
|SAHH_THEMA Adenosylhomocysteinase (Gene Name=ahcY)
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