Structure of PDB 7ocp Chain A Binding Site BS02
Receptor Information
>7ocp Chain A (length=688) Species:
575584
(Acinetobacter baumannii ATCC 19606 = CIP 70.34 = JCM 6841) [
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VLIFHGKPVHGAIFDMDGTMFDTERLRFQTLQQASQELIGQEFSHEYLMQ
CLGLSATTAEKLAQRLYGVDVPYKEIRKRADEMELEHIRKHGVPIKKGLV
QVLERLRKSGLRMAVATSSRRAIAEEYLINANVYKFFDVITCGDEVEQGK
PHPEIFLKAASQLHLDANQCLMFEDSENGLTSAHTSKGLTILLKDIKEPN
DEMLEKAHFYYDQMYDFLTDLDQFIPVMDMPEMQEPFPQSLNQLTVGIHG
FGAIGGGYIAQILSHWDGYTKPKRIIASTRNSLFREAVNAFGTYSIRYGQ
FSYDERIENMSIVDSDNEQQMLEMYTHSSLIALCLPEQAIESESKIIAKG
LYARFNSQLIEPLTFLIILNKVGAKYLVMKHLKEALLELTNDEDVTEHIL
KEHYFCDTVVNRMVSKLSNQNLYRQLRIKHNFLEQHLEDVEQEDQIEIED
CNKLTPDQLNQASIYVDNMRRNFQPGHILQSMDLILFHSETDMPIYVEKG
SPLLEKLRQVVLVDQITDIQLIKNRLWNGVHAMLAWYASLMGYESIGVAM
GDHLVKAFAENLIAEVKQGLAIVLPNYAKDLDRMSQSFLDSCEYAFKDPC
QRVARDPLRKLNHNERVMASIAVNIRHDLPYKNLLKGAALGYAYAIQFLE
IEETKAVEHLQQQIQNLDLSTAQRRQLEAELVQLIQYL
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-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)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=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[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
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[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
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)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
7ocp Chain A Residue 804 [
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Receptor-Ligand Complex Structure
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PDB
7ocp
Unidirectional mannitol synthesis of Acinetobacter baumannii MtlD is facilitated by the helix-loop-helix-mediated dimer formation.
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
G251 F252 A254 I255 T280 R281 C335 L336 P337 A340 L373 N374
Binding residue
(residue number reindexed from 1)
G250 F251 A253 I254 T279 R280 C334 L335 P336 A339 L369 N370
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:7ocp
,
PDBe:7ocp
,
PDBj:7ocp
PDBsum
7ocp
PubMed
35363566
UniProt
D0C7J2
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