메뉴 건너뛰기




Volumn 347, Issue 3, 2005, Pages 623-635

The crystal structure of human PAPS synthetase 1 reveals asymmetry in substrate binding

Author keywords

Adenosine phosphosulfate; Asymmetric homodimer; P loop; Phosphoadenosine phosphosulfate

Indexed keywords

ADENOSINE 3' PHOSPHATE 5' PHOSPHOSULFATE; ADENOSINE DIPHOSPHATE; ADENYLYLSULFATE KINASE; SYNTHETASE;

EID: 14744300141     PISSN: 00222836     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmb.2005.01.005     Document Type: Article
Times cited : (43)

References (36)
  • 1
    • 0042855800 scopus 로고    scopus 로고
    • Tyrosine sulfation of human antibodies contributes to recognition of the CCR5 binding region of HIV-1 gp120
    • H. Choe, W. Li, P. Wright, N. Vasilieva, M. Venturi, and C. Huang Tyrosine sulfation of human antibodies contributes to recognition of the CCR5 binding region of HIV-1 gp120 Cell 114 2003 161 170
    • (2003) Cell , vol.114 , pp. 161-170
    • Choe, H.1    Li, W.2    Wright, P.3    Vasilieva, N.4    Venturi, M.5    Huang, C.6
  • 2
    • 0030996250 scopus 로고    scopus 로고
    • Enzymology of human cytosolic sulfotransferases
    • C. Falany Enzymology of human cytosolic sulfotransferases FASEB J. 11 1997 206 216
    • (1997) FASEB J. , vol.11 , pp. 206-216
    • Falany, C.1
  • 3
    • 0031136606 scopus 로고    scopus 로고
    • The importance of 3′-phosphoadenosine 5′-phosphosulfate (PAPS) in the regulation of sulfation
    • C. Klaassen, and J. Boles The importance of 3′-phosphoadenosine 5′-phosphosulfate (PAPS) in the regulation of sulfation FASEB J. 11 1997 404 418
    • (1997) FASEB J. , vol.11 , pp. 404-418
    • Klaassen, C.1    Boles, J.2
  • 4
    • 17344364658 scopus 로고    scopus 로고
    • Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse
    • M. Faiyaz ul Haque, L. King, D. Krakow, R. Cantor, M. Rusiniak, and R. Swank Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse Nature Genet. 20 1998 157 162
    • (1998) Nature Genet. , vol.20 , pp. 157-162
    • Faiyaz Ul Haque, M.1    King, L.2    Krakow, D.3    Cantor, R.4    Rusiniak, M.5    Swank, R.6
  • 5
    • 0035253851 scopus 로고    scopus 로고
    • Crystal structure of ATP sulfurylase from Saccharomyces cerevisiae, a key enzyme in sulfate activation
    • T. Ullrich, M. Blaesse, and R. Huber Crystal structure of ATP sulfurylase from Saccharomyces cerevisiae, a key enzyme in sulfate activation EMBO J. 20 2001 316 329
    • (2001) EMBO J. , vol.20 , pp. 316-329
    • Ullrich, T.1    Blaesse, M.2    Huber, R.3
  • 6
    • 0035849582 scopus 로고    scopus 로고
    • Crystal structure of ATP sulfurylase from Penicillium chrysogenum: Insights into the allosteric regulation of sulfate assimilation
    • I. MacRae, I. Segel, and A. Fisher Crystal structure of ATP sulfurylase from Penicillium chrysogenum: insights into the allosteric regulation of sulfate assimilation Biochemistry 40 2001 6795 6804
    • (2001) Biochemistry , vol.40 , pp. 6795-6804
    • MacRae, I.1    Segel, I.2    Fisher, A.3
  • 7
    • 0036897415 scopus 로고    scopus 로고
    • Allosteric inhibition via R-state destabilization in ATP sulfurylase from Penicillium chrysogenum
    • I. MacRae, I. Segel, and A. Fisher Allosteric inhibition via R-state destabilization in ATP sulfurylase from Penicillium chrysogenum Nature Struct. Biol. 9 2002 945 949
    • (2002) Nature Struct. Biol. , vol.9 , pp. 945-949
    • MacRae, I.1    Segel, I.2    Fisher, A.3
  • 8
    • 0034701013 scopus 로고    scopus 로고
    • Crystal structure of adenosine 5′-phosphosulfate kinase from Penicillium chrysogenum
    • I. MacRae, I. Segel, and A. Fischer Crystal structure of adenosine 5′-phosphosulfate kinase from Penicillium chrysogenum Biochemistry 39 2000 1613 1621
    • (2000) Biochemistry , vol.39 , pp. 1613-1621
    • MacRae, I.1    Segel, I.2    Fischer, A.3
  • 9
    • 0037137184 scopus 로고    scopus 로고
    • Ligand-induced structural changes in adenosine 5′-phosphosulfate kinase from Penicillium chrysogenum
    • E. Lansdon, I. Segel, and A. Fischer Ligand-induced structural changes in adenosine 5′-phosphosulfate kinase from Penicillium chrysogenum Biochemistry 41 2002 13672 13680
    • (2002) Biochemistry , vol.41 , pp. 13672-13680
    • Lansdon, E.1    Segel, I.2    Fischer, A.3
  • 10
    • 0028335104 scopus 로고
    • Intermediate channeling between atp sulfurylase and adenosine 5′-phosphosulfate kinase from rat chondrosarcoma
    • S. Lyle, D. Ozeran, J. Stanczak, J. Westley, and N. Schwartz Intermediate channeling between atp sulfurylase and adenosine 5′-phosphosulfate kinase from rat chondrosarcoma Biochemistry 33 1994 6822 6827
    • (1994) Biochemistry , vol.33 , pp. 6822-6827
    • Lyle, S.1    Ozeran, D.2    Stanczak, J.3    Westley, J.4    Schwartz, N.5
  • 11
    • 0028865615 scopus 로고
    • A multifunctional Urechis caupo protein, PAPS synthetase, has both ATP sulfurylase and APS kinase activities
    • E. Rosenthal, and T. Leustek A multifunctional Urechis caupo protein, PAPS synthetase, has both ATP sulfurylase and APS kinase activities Gene 165 1995 243 248
    • (1995) Gene , vol.165 , pp. 243-248
    • Rosenthal, E.1    Leustek, T.2
  • 12
    • 0037101780 scopus 로고    scopus 로고
    • Characterization and expression of human bifunctional 3′-phophoadenosine 5′-phosphosulfate synthase isoforms
    • H. Fuda, C. Shimizu, Y. Lee, H. Akita, and C. Strott Characterization and expression of human bifunctional 3′-phophoadenosine 5′- phosphosulfate synthase isoforms Biochem. J. 365 2002 497 504
    • (2002) Biochem. J. , vol.365 , pp. 497-504
    • Fuda, H.1    Shimizu, C.2    Lee, Y.3    Akita, H.4    Strott, C.5
  • 13
    • 4644332108 scopus 로고    scopus 로고
    • Expression, purification and crystallization of human 3′-phospho-adenosine-5′-phosphosulfate synthetase 1
    • S. Harjes, A. Scheidig, and P. Bayer Expression, purification and crystallization of human 3′-phospho-adenosine-5′-phosphosulfate synthetase 1 Acta Crystallog. sect. D 60 2004 350 352
    • (2004) Acta Crystallog. Sect. D , vol.60 , pp. 350-352
    • Harjes, S.1    Scheidig, A.2    Bayer, P.3
  • 14
    • 1842583797 scopus 로고    scopus 로고
    • Human 3′-phosphoadenosine 5′-phosphosulfate synthetase (isoform 1, brain): Kinetic properties of the adenosine triphosphate sulfurylase and adenosine 5′-phosphosulfate kinase domains
    • E. Lansdon, A. Fischer, and I. Segel Human 3′-phosphoadenosine 5′-phosphosulfate synthetase (isoform 1, brain): kinetic properties of the adenosine triphosphate sulfurylase and adenosine 5′-phosphosulfate kinase domains Biochemistry 43 2004 4356 4365
    • (2004) Biochemistry , vol.43 , pp. 4356-4365
    • Lansdon, E.1    Fischer, A.2    Segel, I.3
  • 15
    • 0017411710 scopus 로고
    • The protein data bank: A computer-based archival file for macromolecular structures
    • F. Bernstein, T. Koetzle, G. Williams, E. Meyer Jr., and M. Brice The protein data bank: a computer-based archival file for macromolecular structures J. Mol. Biol. 112 1977 535 542
    • (1977) J. Mol. Biol. , vol.112 , pp. 535-542
    • Bernstein, F.1    Koetzle, T.2    Williams, G.3    Meyer Jr., E.4    Brice, M.5
  • 16
    • 0027440362 scopus 로고
    • Protein structure comparison by alignment of distance matices
    • L. Holm, and C. Sander Protein structure comparison by alignment of distance matices J. Mol. Biol. 233 1993 123 138
    • (1993) J. Mol. Biol. , vol.233 , pp. 123-138
    • Holm, L.1    Sander, C.2
  • 17
    • 0030587517 scopus 로고    scopus 로고
    • The crystal structure of the bifunctional enzyme 6-phosphofructo-2- kinase/fructose-2,6-bisphosphatase reveals distinct domain homologies
    • C. Hasemann, E. Istvan, K. Uyeda, and J. Deisenhofer The crystal structure of the bifunctional enzyme 6-phosphofructo-2-kinase/fructose-2,6- bisphosphatase reveals distinct domain homologies Structure 4 1996 1017 1029
    • (1996) Structure , vol.4 , pp. 1017-1029
    • Hasemann, C.1    Istvan, E.2    Uyeda, K.3    Deisenhofer, J.4
  • 18
    • 0033613863 scopus 로고    scopus 로고
    • Site-selected mutagenesis of a conserved nucleotide binding HXGH motif located in the ATP sulfurylase domain of human bifunctional 3′- phosphoadenosine-5′-phosphosulfate synthetase
    • K. Venkatachalam, H. Fuda, E. Koonin, and C. Strott Site-selected mutagenesis of a conserved nucleotide binding HXGH motif located in the ATP sulfurylase domain of human bifunctional 3′-phosphoadenosine-5′- phosphosulfate synthetase J. Biol. Chem. 274 1999 2601 2604
    • (1999) J. Biol. Chem. , vol.274 , pp. 2601-2604
    • Venkatachalam, K.1    Fuda, H.2    Koonin, E.3    Strott, C.4
  • 19
    • 0033574417 scopus 로고    scopus 로고
    • Activity and stability of recombinant bifunctional rearranged and monofunctional domains of ATP-sulfurylase and adenosine 5′-phosphosulfate kinase
    • A. Deyrup, S. Krishnan, B. Singh, and N. Schwartz Activity and stability of recombinant bifunctional rearranged and monofunctional domains of ATP-sulfurylase and adenosine 5′-phosphosulfate kinase J. Biol. Chem. 274 1999 10751 10757
    • (1999) J. Biol. Chem. , vol.274 , pp. 10751-10757
    • Deyrup, A.1    Krishnan, S.2    Singh, B.3    Schwartz, N.4
  • 20
    • 0032582503 scopus 로고    scopus 로고
    • Adenosine 5′-phosphosulfate kinase from Penicillium chrysogenum
    • I. MacRae, A. Rose, and I. Segel Adenosine 5′-phosphosulfate kinase from Penicillium chrysogenum J. Biol. Chem. 273 1998 28583 28589
    • (1998) J. Biol. Chem. , vol.273 , pp. 28583-28589
    • MacRae, I.1    Rose, A.2    Segel, I.3
  • 21
    • 0032540236 scopus 로고    scopus 로고
    • Deletion and site-directed mutagenesis of the ATP-binding motif in the bifunctional murine ATP-sulfurylase/adenosine 5′-phosphosulfate kinase enzyme
    • A. Deyrup, S. Krishnan, B. Cockburn, and N. Schwartz Deletion and site-directed mutagenesis of the ATP-binding motif in the bifunctional murine ATP-sulfurylase/adenosine 5′-phosphosulfate kinase enzyme J. Biol. Chem. 273 1998 9450 9456
    • (1998) J. Biol. Chem. , vol.273 , pp. 9450-9456
    • Deyrup, A.1    Krishnan, S.2    Cockburn, B.3    Schwartz, N.4
  • 22
    • 0000243829 scopus 로고
    • Procheck - A program to check the stereochemical quality of protein structures
    • R. Laskowski, M. MacArthur, and D.M.J. Thornton Procheck - a program to check the stereochemical quality of protein structures J. Appl. Crystallog. 26 1993 283 291
    • (1993) J. Appl. Crystallog. , vol.26 , pp. 283-291
    • Laskowski, R.1    MacArthur, M.2    Thornton, D.M.J.3
  • 23
    • 0037414823 scopus 로고    scopus 로고
    • Identification and functional characterization of the novel BM-motif in the murine phosphoadenosine phosphosulfate (PAPS) synthetase
    • B. Singh, and N. Schwartz Identification and functional characterization of the novel BM-motif in the murine phosphoadenosine phosphosulfate (PAPS) synthetase J. Biol. Chem. 278 2003 71 75
    • (2003) J. Biol. Chem. , vol.278 , pp. 71-75
    • Singh, B.1    Schwartz, N.2
  • 25
    • 0000560808 scopus 로고    scopus 로고
    • Molrep: An automated program for molecular replacement
    • A. Vagin, and A. Teplyakov Molrep: an automated program for molecular replacement J. Appl. Crystallog. 30 1997 1022 1025
    • (1997) J. Appl. Crystallog. , vol.30 , pp. 1022-1025
    • Vagin, A.1    Teplyakov, A.2
  • 26
    • 0031473847 scopus 로고    scopus 로고
    • SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling
    • N. Guex, and M. Peitsch SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling Electrophoresis 18 1997 27142723
    • (1997) Electrophoresis , vol.18 , pp. 27142723
    • Guex, N.1    Peitsch, M.2
  • 28
    • 0032790081 scopus 로고    scopus 로고
    • Xtalview/Xfit - A versatile program to manipulate atomic coordinates and electron density
    • D. McRee Xtalview/Xfit - a versatile program to manipulate atomic coordinates and electron density J. Struct. Biol. 125 1999 156 165
    • (1999) J. Struct. Biol. , vol.125 , pp. 156-165
    • McRee, D.1
  • 29
    • 0032964481 scopus 로고    scopus 로고
    • Automated protein model building combined with iterative structure refinement
    • A. Perrakis, R. Morris, and V. Lamzin Automated protein model building combined with iterative structure refinement Nature Struct. Biol. 6 1999 458 463
    • (1999) Nature Struct. Biol. , vol.6 , pp. 458-463
    • Perrakis, A.1    Morris, R.2    Lamzin, V.3
  • 30
    • 0030924992 scopus 로고    scopus 로고
    • Refinement of macromolecular structures by the maximum-likelihood method
    • G. Murshudov, A.A. Vagin, and E.J. Dodson Refinement of macromolecular structures by the maximum-likelihood method Acta Crystallog. sect. D 53 1997 240 255
    • (1997) Acta Crystallog. Sect. D , vol.53 , pp. 240-255
    • Murshudov, G.1    Vagin, A.A.2    Dodson, E.J.3
  • 31
    • 0028103275 scopus 로고
    • CCP4 suite: Programs for protein crystallography
    • CCP4
    • CCP4 CCP4 suite: programs for protein crystallography Acta Crystallog. sect. D 50 1994 760 763
    • (1994) Acta Crystallog. Sect. D , vol.50 , pp. 760-763
  • 32
    • 0037495965 scopus 로고    scopus 로고
    • Development of polyphosphate parameters for use with the amber force field
    • K. Meagher, L. Redman, and H. Carlson Development of polyphosphate parameters for use with the amber force field J. Comput. Chem. 24 2003 1016 1025
    • (2003) J. Comput. Chem. , vol.24 , pp. 1016-1025
    • Meagher, K.1    Redman, L.2    Carlson, H.3
  • 33
    • 0027879008 scopus 로고
    • Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants
    • W. Kabsch Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants J. Appl. Crystallog. 26 1993 795 800
    • (1993) J. Appl. Crystallog. , vol.26 , pp. 795-800
    • Kabsch, W.1
  • 34
    • 0032563290 scopus 로고    scopus 로고
    • Molecular cloning, expression, and characterization of human bifunctional 3′-phosphoadenosine 5′-phosphosulfate synthase and its functional domains
    • K. Venkatachalam, H. Akita, and C. Strott Molecular cloning, expression, and characterization of human bifunctional 3′-phosphoadenosine 5′-phosphosulfate synthase and its functional domains J. Biol. Chem. 273 1998 19311 19320
    • (1998) J. Biol. Chem. , vol.273 , pp. 19311-19320
    • Venkatachalam, K.1    Akita, H.2    Strott, C.3
  • 35
    • 0020997912 scopus 로고
    • Dictionary of protein secondary structure: Pattern recognition of hydrogen-bonded and geometrical features
    • W. Kabsch, and C. Sander Dictionary of protein secondary structure: Pattern recognition of hydrogen-bonded and geometrical features Biopolymers 22 1983 2577 2637
    • (1983) Biopolymers , vol.22 , pp. 2577-2637
    • Kabsch, W.1    Sander, C.2
  • 36
    • 0032961270 scopus 로고    scopus 로고
    • ESPript: Multiple sequence alignments in postscript
    • P. Gouet, E. Courcelle, D. Stuart, and F. Metoz ESPript: multiple sequence alignments in postscript Bioinformatics 15 1999 305 308
    • (1999) Bioinformatics , vol.15 , pp. 305-308
    • Gouet, P.1    Courcelle, E.2    Stuart, D.3    Metoz, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.