Structure of PDB 2oo5 Chain A Binding Site BS01
Receptor Information
>2oo5 Chain A (length=380) Species:
1085
(Rhodospirillum rubrum) [
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MKIAIPKERRPGEDRVAISPEVVKKLVGLGFEVIVEQGAGVGASITDDAL
TAAGATIASTAAQALSQADVVWKVQRPMTAEEGTDEVALIKEGAVLMCHL
GALTNRPVVEALTKRKITAYAMELMPRISRAQSMDILSSQSNLAGYRAVI
DGAYEFARAFPMMMTAAGTVPPARVLVFGVGVAGLQAIATAKRLGAVVMA
TDVRAATKEQVESLGGKFITVDDEAMKTAETAGGYAKEMGEEFRKKQAEA
VLKELVKTDIAITTALIPGKPAPVLITEEMVTKMKPGSVIIDLAVEAGGN
CPLSEPGKIVVKHGVKIVGHTNVPSRVAADASPLFAKNLLNFLTPHVDKD
TKTLVMKLEDETVSGTCVTRDGAIVHPALT
Ligand information
Ligand ID
TXD
InChI
InChI=1S/C21H31N7O14P2/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/h1-2,7-11,13-16,20-21,29-32H,3-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t9?,10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
GFDCQHGWOHYWLP-BFAIWXBASA-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)N5CC=CC(C5)C(=O)N)O)O)O)O)N
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)N5CC=CC(C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)[CH]1CN(CC=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
CACTVS 3.341
NC(=O)[C@H]1CN(CC=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
Formula
C21 H31 N7 O14 P2
Name
1,4,5,6-TETRAHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE
ChEMBL
DrugBank
ZINC
PDB chain
2oo5 Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
2oo5
Structures of the dI(2)dIII(1) Complex of Proton-Translocating Transhydrogenase with Bound, Inactive Analogues of NADH and NADPH Reveal Active Site Geometries
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
R127 I128 Q132 D135 D202 V203 R204 G234 A236 Q247 A265 L266 L275
Binding residue
(residue number reindexed from 1)
R127 I128 Q132 D135 D202 V203 R204 G234 A236 Q247 A265 L266 L275
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
R15 Q75 H99 G101 E123 R127 Q132 D135 S138 Y235 E296
Catalytic site (residue number reindexed from 1)
R15 Q75 H99 G101 E123 R127 Q132 D135 S138 Y235 E296
Enzyme Commision number
7.1.1.1
: proton-translocating NAD(P)(+) transhydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003957
NAD(P)+ transhydrogenase (Si-specific) activity
GO:0005515
protein binding
GO:0008750
proton-translocating NAD(P)+ transhydrogenase activity
GO:0016491
oxidoreductase activity
GO:0046983
protein dimerization activity
GO:0050661
NADP binding
GO:0051287
NAD binding
GO:0070403
NAD+ binding
GO:0070404
NADH binding
Biological Process
GO:0006740
NADPH regeneration
GO:1902600
proton transmembrane transport
Cellular Component
GO:0005886
plasma membrane
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2oo5
,
PDBe:2oo5
,
PDBj:2oo5
PDBsum
2oo5
PubMed
17323922
UniProt
Q2RSB2
|PNTAA_RHORT NAD(P) transhydrogenase subunit alpha part 1 (Gene Name=pntAA)
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