Structure of PDB 1l7e Chain D Binding Site BS01
Receptor Information
>1l7e Chain D (length=367) Species:
1085
(Rhodospirillum rubrum) [
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MKIAIPKERRPGEDRVAISPEVVKKLVGLGFEVIVEQGAGVGASITDDAL
TAAGATIASTAAQALSQADVVWKVQRPMTAEEGTDEVALIKEGAVLMCHL
GALTNRPVVEALTKRKITAYAMELMPRISRAQSMDILSSQSNLAGYRAVI
DGAYEFARAFPMMMTAAGTVPPARVLVFGVGVAGLQAIATAKRLGAVVMA
TDVRAATKEQVESLGGKFITVDGGYAKEMGEEFRKKQAEAVLKELVKTDI
AITTALIPGKPAPVLITEEMVTKMKPGSVIIDLAVEAGGNCPLSEPGKIV
VKHGVKIVGHTNVPSRVAADASPLFAKNLLNFLTPHVDKDTKTLVMKLED
ETVSGTCVTRDGAIVHP
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
1l7e Chain D Residue 702 [
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Receptor-Ligand Complex Structure
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PDB
1l7e
Crystal Structures of Transhydrogenase Domain I with and without Bound NADH
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
R1327 I1328 Q1332 D1335 S1338 G1381 D1402 R1404 A1436 Q1447 A1465 L1466 P1473 L1475
Binding residue
(residue number reindexed from 1)
R127 I128 Q132 D135 S138 G181 D202 R204 A226 Q237 A255 L256 P263 L265
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R1215 Q1275 H1299 G1301 E1323 R1327 Q1332 D1335 S1338 Y1435 E1496
Catalytic site (residue number reindexed from 1)
R15 Q75 H99 G101 E123 R127 Q132 D135 S138 Y225 E286
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1l7e
,
PDBe:1l7e
,
PDBj:1l7e
PDBsum
1l7e
PubMed
12379117
UniProt
Q2RSB2
|PNTAA_RHORT NAD(P) transhydrogenase subunit alpha part 1 (Gene Name=pntAA)
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