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Volumn 16, Issue 23, 1997, Pages 7078-7090

Structure of the human NF-κB p52 homodimer-DNA complex at 2.1 A resolution

Author keywords

Crystal structure; NF B p52; Protein DNA interaction; Rel protein; Transcription

Indexed keywords

CELL PROTEIN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; PROTEIN P52; TRANSCRIPTION FACTOR REL; UNCLASSIFIED DRUG;

EID: 0030723630     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (127)

References (55)
  • 1
    • 0030271387 scopus 로고    scopus 로고
    • NF-κB: Ten years after
    • Baeuerle, P.A. and Baltimore, D. (1996) NF-κB: ten years after. Cell, 87, 13-20.
    • (1996) Cell , vol.87 , pp. 13-20
    • Baeuerle, P.A.1    Baltimore, D.2
  • 2
    • 0028174061 scopus 로고
    • Function and activation of NF-κB in the immune system
    • Baeuerle, P.A. and Henkel, T. (1994) Function and activation of NF-κB in the immune system. Annu. Rev. Immunol., 12, 141-179.
    • (1994) Annu. Rev. Immunol. , vol.12 , pp. 141-179
    • Baeuerle, P.A.1    Henkel, T.2
  • 3
    • 0029874138 scopus 로고    scopus 로고
    • The NF-κB and IκB proteins: New discoveries and insights
    • Baldwin, A. (1996) The NF-κB and IκB proteins: new discoveries and insights. Annu. Rev. Immunol., 14, 649-681.
    • (1996) Annu. Rev. Immunol. , vol.14 , pp. 649-681
    • Baldwin, A.1
  • 4
    • 0023080580 scopus 로고
    • Binding of a nuclear factor to a regulatory sequence in the promoter of the mouse H-2 κB class I major histocompatibility gene
    • Baldwin, A., Jr and Sharp, P.A. (1987) Binding of a nuclear factor to a regulatory sequence in the promoter of the mouse H-2 κB class I major histocompatibility gene. Mol. Cell. Biol., 7, 305-313.
    • (1987) Mol. Cell. Biol. , vol.7 , pp. 305-313
    • Baldwin Jr., A.1    Sharp, P.A.2
  • 5
    • 1842287917 scopus 로고
    • Two transcription factors, NF-κB and H2TF1, interact with a single regulatory sequence in the class I major histocompatibility complex promoter
    • Baldwin, A., Jr and Sharp, P.A. (1988) Two transcription factors, NF-κB and H2TF1, interact with a single regulatory sequence in the class I major histocompatibility complex promoter. Proc. Natl Acad. Sci. USA, 85, 723-727.
    • (1988) Proc. Natl Acad. Sci. USA , vol.85 , pp. 723-727
    • Baldwin Jr., A.1    Sharp, P.A.2
  • 6
    • 0029841338 scopus 로고    scopus 로고
    • Immune factor Gambif1, a new rel family member from the human malaria vector, Anopheles gambiae
    • Barillas-Mury, C., Charlesworth, A., Gross, I., Richman, A., Hoffmann, J.A. and Kafatos, F.C. (1996) Immune factor Gambif1, a new rel family member from the human malaria vector, Anopheles gambiae. EMBO J., 15, 4691-4701.
    • (1996) EMBO J. , vol.15 , pp. 4691-4701
    • Barillas-Mury, C.1    Charlesworth, A.2    Gross, I.3    Richman, A.4    Hoffmann, J.A.5    Kafatos, F.C.6
  • 7
    • 0024286247 scopus 로고
    • Mutant Trp repressors with new DNA binding specificities
    • Bass, S., Sorrells, V. and Youderian, P. (1988) Mutant Trp repressors with new DNA binding specificities. Science, 242, 240-245.
    • (1988) Science , vol.242 , pp. 240-245
    • Bass, S.1    Sorrells, V.2    Youderian, P.3
  • 11
    • 0027446955 scopus 로고
    • The oncoprotein Bcl-3 directly transactivates through κB motifs via association with DNA binding p50B homodimers
    • Bours, V., Franzoso, G., Azarenko, V., Park, S., Kanno, T., Brown, K. and Siebenlist, U. (1993) The oncoprotein Bcl-3 directly transactivates through κB motifs via association with DNA binding p50B homodimers. Cell, 72, 729-739.
    • (1993) Cell , vol.72 , pp. 729-739
    • Bours, V.1    Franzoso, G.2    Azarenko, V.3    Park, S.4    Kanno, T.5    Brown, K.6    Siebenlist, U.7
  • 13
    • 0028103275 scopus 로고
    • The CCP4 suite: Programs for protein crystallography
    • Collaborative Computational Project Number 4
    • CCP4 (1994) Collaborative Computational Project Number 4. The CCP4 suite: Programs for protein crystallography. Acta Crystallogr., D50, 760-776.
    • (1994) Acta Crystallogr. , vol.D50 , pp. 760-776
  • 14
    • 0028006556 scopus 로고
    • Mechanism of expression and role in transcriptional control of the proto-oncogene NFKB-2/LYT-10
    • Chang, C.C., Zhang, J., Lombardi, L., Neri, A. and Dalla-Favera, R. (1994) Mechanism of expression and role in transcriptional control of the proto-oncogene NFKB-2/LYT-10. Oncogene, 9, 923-933.
    • (1994) Oncogene , vol.9 , pp. 923-933
    • Chang, C.C.1    Zhang, J.2    Lombardi, L.3    Neri, A.4    Dalla-Favera, R.5
  • 15
    • 0029863521 scopus 로고    scopus 로고
    • The Rel family of eukaryotic transcription factors
    • Chytil, M. and Verdine, G.L. (1996) The Rel family of eukaryotic transcription factors. Curr. Opin. Struct. Biol., 6, 91-100.
    • (1996) Curr. Opin. Struct. Biol. , vol.6 , pp. 91-100
    • Chytil, M.1    Verdine, G.L.2
  • 16
    • 0343907251 scopus 로고    scopus 로고
    • Engineering of diffraction-quality crystals of the NF-κB p52 homodimer-DNA complex
    • Cramer, P. and Müller, C.W. (1997) Engineering of diffraction-quality crystals of the NF-κB p52 homodimer-DNA complex. FEBS Lett., 405, 373-377.
    • (1997) FEBS Lett. , vol.405 , pp. 373-377
    • Cramer, P.1    Müller, C.W.2
  • 18
    • 0027406040 scopus 로고
    • Dimerization of NF-κB2 with RelA(p65) regulates DNA binding, transcriptional activation, and inhibition by an IκB-α (MAD- 3)
    • Duckett, C.S., Perkins, N.D., Kowalik, T.F., Schmid, R.M., Huang, E.S., Baldwin, A., Jr and Nabel, G.J. (1993) Dimerization of NF-κB2 with RelA(p65) regulates DNA binding, transcriptional activation, and inhibition by an IκB-α (MAD-3). Mol. Cell. Biol., 13, 1315-1322.
    • (1993) Mol. Cell. Biol. , vol.13 , pp. 1315-1322
    • Duckett, C.S.1    Perkins, N.D.2    Kowalik, T.F.3    Schmid, R.M.4    Huang, E.S.5    Baldwin Jr., A.6    Nabel, G.J.7
  • 19
    • 0027222103 scopus 로고
    • The oncoprotein Bcl-3 can facilitate NF-κB-mediated transactivation by removing inhibiting p50 homodimers from select κB sites
    • Franzoso, G., Bours, V., Azarenko, V., Park, S., Tomita-Yamaguchi, M., Kanno, T., Brown, K. and Siebenlist, U. (1993) The oncoprotein Bcl-3 can facilitate NF-κB-mediated transactivation by removing inhibiting p50 homodimers from select κB sites. EMBO J., 12, 3893-3901.
    • (1993) EMBO J. , vol.12 , pp. 3893-3901
    • Franzoso, G.1    Bours, V.2    Azarenko, V.3    Park, S.4    Tomita-Yamaguchi, M.5    Kanno, T.6    Brown, K.7    Siebenlist, U.8
  • 20
    • 0028979479 scopus 로고
    • Structure of NF-κB p50 homodimer bound to a κB site
    • Ghosh, G., van Duyne, G., Ghosh, S. and Sigler, P.B. (1995) Structure of NF-κB p50 homodimer bound to a κB site. Nature, 373, 303-310.
    • (1995) Nature , vol.373 , pp. 303-310
    • Ghosh, G.1    Van Duyne, G.2    Ghosh, S.3    Sigler, P.B.4
  • 21
    • 0027333044 scopus 로고
    • The IκB proteins: Members of a multifunctional family
    • Gilmore, T.D. and Morin, P.J. (1993) The IκB proteins: members of a multifunctional family. Trends Genet., 9, 427-433.
    • (1993) Trends Genet. , vol.9 , pp. 427-433
    • Gilmore, T.D.1    Morin, P.J.2
  • 22
    • 0028197265 scopus 로고
    • The bZIP transactivator of Epstein-Barr virus, BZLF1, functionally and physically interacts with the p65 subunit of NF-κB
    • Gutsch, D.E., Holley-Guthrie, E.A., Zhang, Q., Stein, B., Blanar, M.A., Baldwin, A.S. and Kenney, S.C. (1994) The bZIP transactivator of Epstein-Barr virus, BZLF1, functionally and physically interacts with the p65 subunit of NF-κB. Mol. Cell. Biol., 14, 1939-1948.
    • (1994) Mol. Cell. Biol. , vol.14 , pp. 1939-1948
    • Gutsch, D.E.1    Holley-Guthrie, E.A.2    Zhang, Q.3    Stein, B.4    Blanar, M.A.5    Baldwin, A.S.6    Kenney, S.C.7
  • 23
    • 0030003963 scopus 로고    scopus 로고
    • Propeller-twisting of base-pairs and the conformational mobility of dinucleotide steps in DNA
    • Hassan, M.A.E. and Calladine, C.R. (1996) Propeller-twisting of base-pairs and the conformational mobility of dinucleotide steps in DNA. J. Mol. Biol., 259, 95-103.
    • (1996) J. Mol. Biol. , vol.259 , pp. 95-103
    • Hassan, M.A.E.1    Calladine, C.R.2
  • 24
    • 0028157348 scopus 로고
    • Mutagenesis supports water mediated recognition in the trp repressor-operator system
    • Joachimiak, A., Haran, T.E. and Sigler, P.B. (1994) Mutagenesis supports water mediated recognition in the trp repressor-operator system. EMBO J., 13, 367-372.
    • (1994) EMBO J. , vol.13 , pp. 367-372
    • Joachimiak, A.1    Haran, T.E.2    Sigler, P.B.3
  • 25
    • 84889120137 scopus 로고
    • Improved methods for building protein models in electron density maps and the location of errors in these models
    • Jones, A.T., Zhou, J.-Y., Cowan, S.W. and Kjeldgaard, M. (1991) Improved methods for building protein models in electron density maps and the location of errors in these models. Acta Crystallogr., A47, 110-119.
    • (1991) Acta Crystallogr. , vol.A47 , pp. 110-119
    • Jones, A.T.1    Zhou, J.-Y.2    Cowan, S.W.3    Kjeldgaard, M.4
  • 26
    • 0026244229 scopus 로고
    • MOLSCRIPT: A program to produce both detailed and schematic plots of protein structures
    • Kraulis, P.J. (1991) MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures. J. Appl. Crystallogr., 24, 946-950.
    • (1991) J. Appl. Crystallogr. , vol.24 , pp. 946-950
    • Kraulis, P.J.1
  • 27
    • 0026652879 scopus 로고
    • The RxxRxRxxC motif conserved in all Rel/κB proteins is essential for the DNA binding activity and redox regulation of the v-Rel oncoprotein
    • Kumar, S., Rabson, A.B. and Gelinas, C. (1992) The RxxRxRxxC motif conserved in all Rel/κB proteins is essential for the DNA binding activity and redox regulation of the v-Rel oncoprotein. Mol. Cell. Biol., 12, 3094-3106.
    • (1992) Mol. Cell. Biol. , vol.12 , pp. 3094-3106
    • Kumar, S.1    Rabson, A.B.2    Gelinas, C.3
  • 28
    • 0031591393 scopus 로고    scopus 로고
    • Electrostatics and hydration at the homeodomain-DNA interface: Chemical probes of an interfacial water cavity
    • Labeots, L.A. and Weiss, M.A. (1997) Electrostatics and hydration at the homeodomain-DNA interface: chemical probes of an interfacial water cavity. J. Mol. Biol., 269, 113-128.
    • (1997) J. Mol. Biol. , vol.269 , pp. 113-128
    • Labeots, L.A.1    Weiss, M.A.2
  • 29
    • 0000243829 scopus 로고
    • PROCHECK: A program to check the stereochemical quality of protein structures
    • Laskowski, R.A., MacArthur, M.W., Moss, D.S. and Thornton, J.M. (1993) PROCHECK: a program to check the stereochemical quality of protein structures. J. Appl. Crystallogr., 26, 283-291.
    • (1993) J. Appl. Crystallogr. , vol.26 , pp. 283-291
    • Laskowski, R.A.1    MacArthur, M.W.2    Moss, D.S.3    Thornton, J.M.4
  • 30
    • 0024058085 scopus 로고
    • The definition of generalized helicoidal parameters and of axis curvature for irregular nucleic acids
    • Lavery, R. and Sklenar, H. (1988) The definition of generalized helicoidal parameters and of axis curvature for irregular nucleic acids. J. Biomol. Struct. Dynam., 6, 63-91.
    • (1988) J. Biomol. Struct. Dynam. , vol.6 , pp. 63-91
    • Lavery, R.1    Sklenar, H.2
  • 31
    • 0015222647 scopus 로고
    • The interpretation of protein structures: Estimation of static accessibility
    • Lee, B. and Richards, F.M. (1971) The interpretation of protein structures: estimation of static accessibility. J. Mol. Biol., 55, 379-400.
    • (1971) J. Mol. Biol. , vol.55 , pp. 379-400
    • Lee, B.1    Richards, F.M.2
  • 32
    • 0028854272 scopus 로고
    • Differential transcriptional activation in vitro by NF-κB/Rel proteins
    • Lin, R., Gewert, D. and Hiscott, J. (1995) Differential transcriptional activation in vitro by NF-κB/Rel proteins. J. Biol. Chem., 270, 3123-3131.
    • (1995) J. Biol. Chem. , vol.270 , pp. 3123-3131
    • Lin, R.1    Gewert, D.2    Hiscott, J.3
  • 33
    • 0014432781 scopus 로고
    • Solvent content of protein crystals
    • Matthews, B.W. (1968) Solvent content of protein crystals. J. Mol. Biol., 33, 491-497.
    • (1968) J. Mol. Biol. , vol.33 , pp. 491-497
    • Matthews, B.W.1
  • 34
    • 0028057108 scopus 로고
    • Raster3D Version 2.0-a program for photorealistic molecular graphics
    • Merritt, E.A. and Murphy, M.E.P. (1994) Raster3D Version 2.0-a program for photorealistic molecular graphics. Acta Crystallogr., D50, 869-873.
    • (1994) Acta Crystallogr. , vol.D50 , pp. 869-873
    • Merritt, E.A.1    Murphy, M.E.P.2
  • 36
    • 0030094490 scopus 로고    scopus 로고
    • Comparison of two different DNA-binding modes of the NF-κB p50 homodimer
    • Müller, C.W., Rey, F.A. and Harrison, S.C. (1996) Comparison of two different DNA-binding modes of the NF-κB p50 homodimer. Nature Struct. Biol., 3, 224-227.
    • (1996) Nature Struct. Biol. , vol.3 , pp. 224-227
    • Müller, C.W.1    Rey, F.A.2    Harrison, S.C.3
  • 37
    • 84920325457 scopus 로고
    • AMoRe: An automated program package for molecular replacement
    • Navaza, J. (1994) AMoRe: an automated program package for molecular replacement. Acta Crystallogr., A50, 157-163.
    • (1994) Acta Crystallogr. , vol.A50 , pp. 157-163
    • Navaza, J.1
  • 38
    • 0028245317 scopus 로고
    • NF-AT-AP-1 and Rel-bZIP: Hybrid vigor and binding under the influence
    • Nolan, G.P. (1994) NF-AT-AP-1 and Rel-bZIP: hybrid vigor and binding under the influence. Cell, 77, 795-798.
    • (1994) Cell , vol.77 , pp. 795-798
    • Nolan, G.P.1
  • 39
    • 0031059866 scopus 로고    scopus 로고
    • Processing of X-ray diffraction data collected in oscillation mode
    • Otwinowski, Z. and Minor, W. (1997) Processing of X-ray diffraction data collected in oscillation mode. Methods Enzymol., 276, 307-326.
    • (1997) Methods Enzymol. , vol.276 , pp. 307-326
    • Otwinowski, Z.1    Minor, W.2
  • 41
    • 0026546865 scopus 로고
    • Distinct combinations of NF-κB subunits determine the specificity of transcriptional activation
    • Perkins, N.D., Schmid, R.M., Duckett, C.S., Leung, K., Rice, N.R. and Nabel, G.J. (1992) Distinct combinations of NF-κB subunits determine the specificity of transcriptional activation. Proc. Natl Acad. Sci. USA, 89, 1529-1533.
    • (1992) Proc. Natl Acad. Sci. USA , vol.89 , pp. 1529-1533
    • Perkins, N.D.1    Schmid, R.M.2    Duckett, C.S.3    Leung, K.4    Rice, N.R.5    Nabel, G.J.6
  • 42
    • 12644271902 scopus 로고    scopus 로고
    • A critical arginine residue mediates cooperativity in the contact interface between transcription factors NFAT and AP-1
    • Peterson, B.R., Sun, L.J. and Verdine, G.L. (1996) A critical arginine residue mediates cooperativity in the contact interface between transcription factors NFAT and AP-1. Proc. Natl Acad. Sci. USA, 93, 13671-13676.
    • (1996) Proc. Natl Acad. Sci. USA , vol.93 , pp. 13671-13676
    • Peterson, B.R.1    Sun, L.J.2    Verdine, G.L.3
  • 43
    • 0027291015 scopus 로고
    • Prediction of protein secondary structure at better than 70% accuracy
    • Rost, B. and Sander, C. (1993) Prediction of protein secondary structure at better than 70% accuracy. J. Mol. Biol., 232, 584-599.
    • (1993) J. Mol. Biol. , vol.232 , pp. 584-599
    • Rost, B.1    Sander, C.2
  • 44
    • 0029889988 scopus 로고    scopus 로고
    • PHD: Predicting one-dimensional protein structure by profile-based neural networks
    • Rost, B. (1996) PHD: predicting one-dimensional protein structure by profile-based neural networks. Methods Enzymol., 266, 525-539.
    • (1996) Methods Enzymol. , vol.266 , pp. 525-539
    • Rost, B.1
  • 45
    • 0025738076 scopus 로고
    • Cloning of an NF-κB subunit which stimulates HIV transcription in synergy with p65
    • Schmid, R.M., Perkins, N.D., Duckett, C.S., Andrews, P.C. and Nabel, G.J. (1991) Cloning of an NF-κB subunit which stimulates HIV transcription in synergy with p65. Nature, 352, 733-736.
    • (1991) Nature , vol.352 , pp. 733-736
    • Schmid, R.M.1    Perkins, N.D.2    Duckett, C.S.3    Andrews, P.C.4    Nabel, G.J.5
  • 46
    • 0028579755 scopus 로고
    • Structural and functional analysis of NF-κB. Determinants of DNA binding specificity and protein interaction
    • Schmid, R.M., Liptay, S., Betts, J.C. and Nabel, G.J. (1994) Structural and functional analysis of NF-κB. Determinants of DNA binding specificity and protein interaction. J. Biol. Chem., 269, 32162-32167.
    • (1994) J. Biol. Chem. , vol.269 , pp. 32162-32167
    • Schmid, R.M.1    Liptay, S.2    Betts, J.C.3    Nabel, G.J.4
  • 47
    • 0031047683 scopus 로고    scopus 로고
    • The role of water in protein-DNA interactions
    • Schwabe, J.W. (1997) The role of water in protein-DNA interactions. Curr. Opin. Struct. Biol., 7, 126-134.
    • (1997) Curr. Opin. Struct. Biol. , vol.7 , pp. 126-134
    • Schwabe, J.W.1
  • 48
    • 0027379055 scopus 로고
    • Distinct mechanisms for regulation of the interleukin-8 gene involve synergism and cooperativity between C/EBP and NF-κB
    • Stein, B. and Baldwin, A., Jr (1993) Distinct mechanisms for regulation of the interleukin-8 gene involve synergism and cooperativity between C/EBP and NF-κB. Mol. Cell. Biol., 13, 7191-7198.
    • (1993) Mol. Cell. Biol. , vol.13 , pp. 7191-7198
    • Stein, B.1    Baldwin Jr., A.2
  • 49
    • 0027224017 scopus 로고
    • Cross-coupling of the NF-κB p65 and Fos/ Jun transcription factors produces potentiated biological function
    • Stein, B., Baldwin, A., Jr. Ballard, D.W., Greene, W.C., Angel, P. and Herrlich, P. (1993a) Cross-coupling of the NF-κB p65 and Fos/ Jun transcription factors produces potentiated biological function. EMBO J., 12, 3879-3891.
    • (1993) EMBO J. , vol.12 , pp. 3879-3891
    • Stein, B.1    Baldwin Jr., A.2    Ballard, D.W.3    Greene, W.C.4    Angel, P.5    Herrlich, P.6
  • 50
    • 0027316201 scopus 로고
    • Functional and physical associations between NF-κB and C/EBP family members: A Rel domain-bZIP interaction
    • Stein, B., Cogswell, P.C. and Baldwin, A., Jr (1993b) Functional and physical associations between NF-κB and C/EBP family members: a Rel domain-bZIP interaction. Mol. Cell. Biol., 13, 3964-3974.
    • (1993) Mol. Cell. Biol. , vol.13 , pp. 3964-3974
    • Stein, B.1    Cogswell, P.C.2    Baldwin Jr., A.3
  • 51
    • 0026489365 scopus 로고
    • The high mobility group protein HMG I(Y) is required for NF-κB-dependent virus induction of the human IFN-β gene
    • Thanos, D. and Maniatis, T. (1992) The high mobility group protein HMG I(Y) is required for NF-κB-dependent virus induction of the human IFN-β gene. Cell, 71, 777-789.
    • (1992) Cell , vol.71 , pp. 777-789
    • Thanos, D.1    Maniatis, T.2
  • 52
    • 0028986193 scopus 로고
    • NF-κB: A lesson in family values
    • Thanos, D. and Maniatis, T. (1995) NF-κB: a lesson in family values. Cell, 80, 529-532.
    • (1995) Cell , vol.80 , pp. 529-532
    • Thanos, D.1    Maniatis, T.2
  • 53
    • 0025398721 scopus 로고
    • WHAT IF: A molecular modeling and drug design program
    • Vriend, G. (1990) WHAT IF: a molecular modeling and drug design program. J. Mol. Graph., 8, 52-56.
    • (1990) J. Mol. Graph. , vol.8 , pp. 52-56
    • Vriend, G.1
  • 54
    • 0029160486 scopus 로고
    • High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA
    • Wilson, D.S., Guenther, B., Desplan, C. and Kuriyan, J. (1995) High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA. Cell, 82, 709-719.
    • (1995) Cell , vol.82 , pp. 709-719
    • Wilson, D.S.1    Guenther, B.2    Desplan, C.3    Kuriyan, J.4


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