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Open data
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Basic information
Entry | Database: PDB / ID: 1nk2 | ||||||
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Title | VND/NK-2 HOMEODOMAIN/DNA COMPLEX, NMR, 20 STRUCTURES | ||||||
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![]() | DNA BINDING PROTEIN/DNA / HOMEODOMAIN / HOMEOBOX / DNA-BINDING PROTEIN / EMBRYONIC DEVELOPMENT / COMPLEX (HOMEODOMAIN-DNA) / DNA BINDING PROTEIN-DNA COMPLEX | ||||||
Function / homology | ![]() neuroblast development / neuroblast fate determination / glial cell development / brain development / DNA-binding transcription factor binding / DNA-binding transcription factor activity, RNA polymerase II-specific / cell differentiation / RNA polymerase II cis-regulatory region sequence-specific DNA binding / negative regulation of gene expression / regulation of transcription by RNA polymerase II ...neuroblast development / neuroblast fate determination / glial cell development / brain development / DNA-binding transcription factor binding / DNA-binding transcription factor activity, RNA polymerase II-specific / cell differentiation / RNA polymerase II cis-regulatory region sequence-specific DNA binding / negative regulation of gene expression / regulation of transcription by RNA polymerase II / negative regulation of transcription by RNA polymerase II / positive regulation of transcription by RNA polymerase II / nucleus Similarity search - Function | ||||||
Biological species | ![]() ![]() | ||||||
Method | SOLUTION NMR / DISTANCE GEOMETRY, SIMULATED ANNEALING | ||||||
![]() | Gruschus, J.M. / Tsao, D.H.H. / Wang, L.-H. / Nirenberg, M. / Ferretti, J.A. | ||||||
![]() | ![]() Title: Interactions of the vnd/NK-2 homeodomain with DNA by nuclear magnetic resonance spectroscopy: basis of binding specificity. Authors: Gruschus, J.M. / Tsao, D.H. / Wang, L.H. / Nirenberg, M. / Ferretti, J.A. #1: ![]() Title: Interactions of the Vnd/Nk-2 Homeodomain with DNA by Nuclear Magnetic Resonance Spectroscopy: Basis of Binding Specificity Authors: Gruschus, J.M. / Tsao, D.H. / Wang, L.H. / Nirenberg, M. / Ferretti, J.A. #2: ![]() Title: The Three-Dimensional Solution Structure of the Nk-2 Homeodomain from Drosophila Authors: Tsao, D.H. / Gruschus, J.M. / Wang, L.H. / Nirenberg, M. / Ferretti, J.A. #3: ![]() Title: Elongation of Helix III of the Nk-2 Homeodomain Upon Binding to DNA: A Secondary Structure Study by NMR Authors: Tsao, D.H. / Gruschus, J.M. / Wang, L.H. / Nirenberg, M. / Ferretti, J.A. | ||||||
History |
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Structure visualization
Structure viewer | Molecule: ![]() ![]() |
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Downloads & links
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Download
PDBx/mmCIF format | ![]() | 927.6 KB | Display | ![]() |
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PDB format | ![]() | 770.8 KB | Display | ![]() |
PDBx/mmJSON format | ![]() | Tree view | ![]() | |
Others | ![]() |
-Validation report
Summary document | ![]() | 384.4 KB | Display | ![]() |
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Full document | ![]() | 799.4 KB | Display | |
Data in XML | ![]() | 81.1 KB | Display | |
Data in CIF | ![]() | 106.7 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
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Assembly
Deposited unit | ![]()
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NMR ensembles |
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Components
#1: DNA chain | Mass: 4960.211 Da / Num. of mol.: 1 / Source method: obtained synthetically |
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#2: DNA chain | Mass: 4836.171 Da / Num. of mol.: 1 / Source method: obtained synthetically |
#3: Protein | Mass: 9374.741 Da / Num. of mol.: 1 / Fragment: HOMEODOMAIN Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() ![]() ![]() ![]() |
-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR | ||||||||||||||||||||||||||||
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NMR experiment |
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NMR details | Text: THIS IS THE ENSEMBLE OF 20 STRUCTURES. |
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Sample preparation
Details | Contents: H2O |
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Sample conditions | Ionic strength: 60mM / pH: 6 / Pressure: 1 atm / Temperature: 308 K |
Crystal grow | *PLUS Method: other / Details: NMR |
-NMR measurement
NMR spectrometer | Type: Bruker AMX600 / Manufacturer: Bruker / Model: AMX600 / Field strength: 600 MHz |
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Processing
NMR software |
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Refinement | Method: DISTANCE GEOMETRY, SIMULATED ANNEALING / Software ordinal: 1 / Details: NMR REFINE/INSIGHT II 97 | |||||||||
NMR ensemble | Conformer selection criteria: LEAST RESTRAINT VIOLATION / Conformers calculated total number: 80 / Conformers submitted total number: 20 |