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2KMO
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2kmo
SOLUTION STRUCTURE OF NATIVE LEECH-DERIVED TRYPTASE INHIBITOR, LDTI
Descriptor:Leech-derived tryptase inhibitor C
Authors:Pantoja-Uceda, D., Santoro, J.
Deposit date:2009-08-03
Release date:2009-11-10
Modification date:2011-08-10
Method:SOLUTION NMR
Cite:Deciphering the structural basis that guides the oxidative folding of leech-derived tryptase inhibitor.
J.Biol.Chem., 284, 2009
2KMP
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2kmp
SOLUTION STRUCTURE OF INTERMEIDATE IIA OF LEECK-DERIVED TRYPTASE INHIBITOR, LDTI.
Descriptor:Leech-derived tryptase inhibitor C
Authors:Pantoja-Uceda, D., Santoro, J.
Deposit date:2009-08-03
Release date:2009-11-10
Modification date:2011-08-10
Method:SOLUTION NMR
Cite:Deciphering the structural basis that guides the oxidative folding of leech-derived tryptase inhibitor.
J.Biol.Chem., 284, 2009
2KMQ
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2kmq
SOLUTION STRUCTURE OF INTERMEDIATE IIB OF LEECH-DERIVED TRYPTASE INHIBITOR, LDTI.
Descriptor:Leech-derived tryptase inhibitor C
Authors:Pantoja-Uceda, D., Santoro, J.
Deposit date:2009-08-03
Release date:2009-11-10
Modification date:2011-08-10
Method:SOLUTION NMR
Cite:Deciphering the structural basis that guides the oxidative folding of leech-derived tryptase inhibitor.
J.Biol.Chem., 284, 2009
2KMR
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2kmr
SOLUTION STRUCTURE OF INTERMEDIATE IIC OF LEECH-DERIVED TRYPTASE INHIBITOR, LDTI.
Descriptor:Leech-derived tryptase inhibitor C
Authors:Pantoja-Uceda, D., Santoro, J.
Deposit date:2009-08-03
Release date:2009-11-10
Modification date:2011-08-10
Method:SOLUTION NMR
Cite:Deciphering the structural basis that guides the oxidative folding of leech-derived tryptase inhibitor.
J.Biol.Chem., 284, 2009
3PIS
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3pis
CRYSTAL STRUCTURE OF CARCINOSCORPIUS ROTUNDICAUDA SERINE PROTEASE INHIBITOR DOMAIN 1
Descriptor:Kazal-type serine protease inhibitor SPI-1
Authors:Giri, P.K., Tang, X.H., Sivaraman, J.
Deposit date:2010-11-08
Release date:2010-12-08
Method:X-RAY DIFFRACTION (2 Å)
Cite:Modifying the Substrate Specificity of Carcinoscorpius rotundicauda Serine Protease Inhibitor Domain 1 to Target Thrombin
To be Published
1AN1
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1an1
LEECH-DERIVED TRYPTASE INHIBITOR/TRYPSIN COMPLEX
Descriptor:TRYPTASE INHIBITOR, TRYPSIN
Authors:Priestle, J.P., Di Marco, S.
Deposit date:1997-06-26
Release date:1998-07-01
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.03 Å)
Cite:Structure of the complex of leech-derived tryptase inhibitor (LDTI) with trypsin and modeling of the LDTI-tryptase system.
Structure, 5, 1997
1BMO
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1bmo
BM-40, FS/EC DOMAIN PAIR
Descriptor:BM-40
Authors:Hohenester, E., Maurer, P., Timpl, R.
Deposit date:1997-03-25
Release date:1997-10-15
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (3.1 Å)
Cite:Crystal structure of a pair of follistatin-like and EF-hand calcium-binding domains in BM-40.
EMBO J., 16, 1997
1BUS
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1bus
SOLUTION CONFORMATION OF PROTEINASE INHIBITOR IIA FROM BULL SEMINAL PLASMA BY 1H NUCLEAR MAGNETIC RESONANCE AND DISTANCE GEOMETRY
Descriptor:PROTEINASE INHIBITOR IIA (BUSI IIA) (NMR, 5 DISTANCE CONSTRAINED STRUCTURES)
Authors:Guntert, P., Williamson, M.P., Havel, T.F., Wuthrich, K.
Deposit date:1990-05-14
Release date:1991-04-15
Modification date:2009-02-24
Method:SOLUTION NMR
Cite:Solution conformation of proteinase inhibitor IIA from bull seminal plasma by 1H nuclear magnetic resonance and distance geometry.
J.Mol.Biol., 182, 1985
1CGI
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1cgi
THREE-DIMENSIONAL STRUCTURE OF THE COMPLEXES BETWEEN BOVINE CHYMOTRYPSINOGEN*A AND TWO RECOMBINANT VARIANTS OF HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL-TYPE)
Descriptor:ALPHA-CHYMOTRYPSINOGEN COMPLEX WITH HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR VARIANT 3
Authors:Hecht, H.J., Szardenings, M., Collins, J., Schomburg, D.
Deposit date:1991-10-08
Release date:1993-10-31
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Three-dimensional structure of the complexes between bovine chymotrypsinogen A and two recombinant variants of human pancreatic secretory trypsin inhibitor (Kazal-type).
J.Mol.Biol., 220, 1991
1CGJ
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1cgj
THREE-DIMENSIONAL STRUCTURE OF THE COMPLEXES BETWEEN BOVINE CHYMOTRYPSINOGEN*A AND TWO RECOMBINANT VARIANTS OF HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL-TYPE)
Descriptor:ALPHA-CHYMOTRYPSINOGEN COMPLEX WITH HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR VARIANT 4
Authors:Hecht, H.J., Szardenings, M., Collins, J., Schomburg, D.
Deposit date:1991-10-08
Release date:1993-10-31
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Three-dimensional structure of the complexes between bovine chymotrypsinogen A and two recombinant variants of human pancreatic secretory trypsin inhibitor (Kazal-type).
J.Mol.Biol., 220, 1991
1CHO
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1cho
CRYSTAL AND MOLECULAR STRUCTURES OF THE COMPLEX OF ALPHA-*CHYMOTRYPSIN WITH ITS INHIBITOR TURKEY OVOMUCOID THIRD DOMAIN AT 1.8 ANGSTROMS RESOLUTION
Descriptor:PROTEIN
Authors:Fujinaga, M., Sielecki, A.R., Read, R.J., Ardelt, W., Laskowskijunior, M., James, M.N.G.
Deposit date:1988-03-04
Release date:1988-07-16
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Crystal and molecular structures of the complex of alpha-chymotrypsin with its inhibitor turkey ovomucoid third domain at 1.8 A resolution.
J.Mol.Biol., 195, 1987
1CSO
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1cso
CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-ILE18I IN COMPLEX WITH SGPB
Descriptor:PROTEINASE B (SGPB)/TURKEY OVOMUCOID INHIBITOR
Authors:Bateman, K.S., Anderson, S., Lu, W., Qasim, M.A., Laskowski Jr., M., James, M.N.G.
Deposit date:1999-08-18
Release date:2000-01-12
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Deleterious effects of beta-branched residues in the S1 specificity pocket of Streptomyces griseus proteinase B (SGPB): crystal structures of the turkey ovomucoid third domain variants Ile18I, Val18I, Thr18I, and Ser18I in complex with SGPB.
Protein Sci., 9, 2000
1CT0
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1ct0
CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-SER18I IN COMPLEX WITH SGPB
Descriptor:PROTEINASE B (SBPB)/TURKEY OVOMUCOID INHIBITOR
Authors:Bateman, K.S., Anderson, S., Lu, W., Qasim, M.A., Laskowski Jr., M., James, M.N.G.
Deposit date:1999-08-18
Release date:2000-01-12
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.8 Å)
Cite:Deleterious effects of beta-branched residues in the S1 specificity pocket of Streptomyces griseus proteinase B (SGPB): crystal structures of the turkey ovomucoid third domain variants Ile18I, Val18I, Thr18I, and Ser18I in complex with SGPB.
Protein Sci., 9, 2000
1CT2
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1ct2
CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-THR18I IN COMPLEX WITH SGPB
Descriptor:PROTEINASE B (SGPB)/TURKEY OVOMUCOID INHIBITOR
Authors:Bateman, K.S., Anderson, S., Lu, W., Qasim, M.A., Laskowski Jr., M., James, M.N.
Deposit date:1999-08-18
Release date:2000-01-12
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.65 Å)
Cite:Deleterious effects of beta-branched residues in the S1 specificity pocket of Streptomyces griseus proteinase B (SGPB): crystal structures of the turkey ovomucoid third domain variants Ile18I, Val18I, Thr18I, and Ser18I in complex with SGPB.
Protein Sci., 9, 2000
1CT4
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1ct4
CRYSTAL STRUCTURE OF THE OMTKY3 P1 VARIANT OMTKY3-VAL18I IN COMPLEX WITH SGPB
Descriptor:PROTEINASE B (SGPB)/TURKEY OVOMUCOID INHIBITOR
Authors:Bateman, K.S., Anderson, S., Lu, W., Qasim, M.A., Laskowski Jr., M., James, M.N.G.
Deposit date:1999-08-18
Release date:2000-01-12
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.6 Å)
Cite:Deleterious effects of beta-branched residues in the S1 specificity pocket of Streptomyces griseus proteinase B (SGPB): crystal structures of the turkey ovomucoid third domain variants Ile18I, Val18I, Thr18I, and Ser18I in complex with SGPB.
Protein Sci., 9, 2000
1DS2
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1ds2
CRYSTAL STRUCTURE OF SGPB:OMTKY3-COO-LEU18I
Descriptor:CRYSTAL STRUCTURE OF SGPB:OMTKY3-COO-LEU18I
Authors:Bateman, K.S., Huang, K., Anderson, S., Lu, W., Qasim, M.A., Laskowski Jr., M., James, M.N.G.
Deposit date:2000-01-06
Release date:2001-01-31
Modification date:2011-07-13
Method:X-RAY DIFFRACTION (1.7 Å)
Cite:Contribution of peptide bonds to inhibitor-protease binding: crystal structures of the turkey ovomucoid third domain backbone variants OMTKY3-Pro18I and OMTKY3-psi[COO]-Leu18I in complex with Streptomyces griseus proteinase B (SGPB) and the structure of the free inhibitor, OMTKY-3-psi[CH2NH2+]-Asp19I
J.Mol.Biol., 305, 2001
1DS3
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1ds3
CRYSTAL STRUCTURE OF OMTKY3-CH2-ASP19I
Descriptor:CRYSTAL STRUCTURE OF OMTKY3-CH2-ASP19I
Authors:Bateman, K.S., Huang, K., Anderson, S., Lu, W., Qasim, M.A., Laskowski Jr., M., James, M.N.G.
Deposit date:2000-01-06
Release date:2001-01-31
Modification date:2011-08-17
Method:X-RAY DIFFRACTION (1.65 Å)
Cite:Contribution of peptide bonds to inhibitor-protease binding: crystal structures of the turkey ovomucoid third domain backbone variants OMTKY3-Pro18I and OMTKY3-psi[COO]-Leu18I in complex with Streptomyces griseus proteinase B (SGPB) and the structure of the free inhibitor, OMTKY-3-psi[CH2NH2+]-Asp19I
J.Mol.Biol., 305, 2001
1H0Z
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1h0z
LEKTI DOMAIN SIX
Descriptor:SERINE PROTEASE INHIBITOR KAZAL-TYPE 5, CONTAINS HEMOFILTRATE PEPTIDE HF6478, HEMOFILTRATE PEPTIDE HF7665
Authors:Lauber, T., Roesch, P., Marx, U.C.
Deposit date:2002-07-01
Release date:2003-06-26
Modification date:2009-02-24
Method:SOLUTION NMR
Cite:Homologous Proteins with Different Folds: The Three-Dimensional Structures of Domains 1 and 6 of the Multiple Kazal-Type Inhibitor Lekti
J.Mol.Biol., 328, 2003
1HJA
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1hja
LYS 18 VARIANT OF TURKEY OVOMUCOID INHIBITOR THIRD DOMAIN COMPLEXED WITH ALPHA-CHYMOTRYPSIN
Descriptor:ALPHA-CHYMOTRYPSIN, OVOMUCOID INHIBITOR
Authors:Ding, J.-H., James, M.N.G.
Deposit date:1997-07-09
Release date:1998-01-14
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Crystal Structure of Lys18 Variant of Turkey Ovomucoid Inhibitor Third Domain Complexed with Alpha-Chymotrypsin at 2.3 A
To be Published
1HPT
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1hpt
THREE-DIMENSIONAL STRUCTURE OF A RECOMBINANT VARIANT OF HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR (KAZAL TYPE)
Descriptor:HUMAN PANCREATIC SECRETORY TRYPSIN INHIBITOR VARIANT 3
Authors:Hecht, H.J., Szardenings, M., Collins, J., Schomburg, D.
Deposit date:1992-03-27
Release date:1993-10-31
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Three-dimensional structure of a recombinant variant of human pancreatic secretory trypsin inhibitor (Kazal type).
J.Mol.Biol., 225, 1992
1IY5
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1iy5
SOLUTION STRUCTURE OF WILD TYPE OMSVP3
Descriptor:Ovomucoid
Authors:Hemmi, H., Kumazaki, T., Yamazaki, T., Kojima, S., Yoshida, T., Kyogoku, Y., Katsu, M., Yokosawa, H., Miura, K., Kobayashi, Y.
Deposit date:2002-07-23
Release date:2003-03-11
Modification date:2009-02-24
Method:SOLUTION NMR
Cite:Inhibitory Specificity Change of Ovomucoid Third Domain of the Silver Pheasant upon Introduction of an Engineered Cys14-Cys39 Bond
BIOCHEMISTRY, 42, 2003
1IY6
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1iy6
SOLUTION STRUCTURE OF OMSVP3 VARIANT, P14C/N39C
Descriptor:Ovomucoid
Authors:Hemmi, H., Kumazaki, T., Yamazaki, T., Kojima, S., Yoshida, T., Kyogoku, Y., Katsu, M., Yokosawa, H., Miura, K., Kobayashi, Y.
Deposit date:2002-07-23
Release date:2003-03-11
Modification date:2009-02-24
Method:SOLUTION NMR
Cite:Inhibitory Specificity Change of Ovomucoid Third Domain of the Silver Pheasant upon Introduction of an Engineered Cys14-Cys39 Bond
BIOCHEMISTRY, 42, 2003
1KMA
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1kma
NMR STRUCTURE OF THE DOMAIN-I OF THE KAZAL-TYPE THROMBIN INHIBITOR DIPETALIN
Descriptor:DIPETALIN
Authors:Schlott, B., Wohnert, J., Icke, C., Hartmann, M., Ramachandran, R., Guhrs, K.-H., Glusa, E., Flemming, J., Gorlach, M., Grosse, F., Ohlenschlager, O.
Deposit date:2001-12-14
Release date:2002-05-15
Modification date:2009-02-24
Method:SOLUTION NMR
Cite:Interaction of Kazal-type inhibitor domains with serine proteinases: biochemical and structural studies.
J.Mol.Biol., 318, 2002
1LDT
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1ldt
COMPLEX OF LEECH-DERIVED TRYPTASE INHIBITOR WITH PORCINE TRYPSIN
Descriptor:TRYPSIN, TRYPTASE INHIBITOR
Authors:Stubbs, M.T.
Deposit date:1997-05-15
Release date:1998-05-20
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:The three-dimensional structure of recombinant leech-derived tryptase inhibitor in complex with trypsin. Implications for the structure of human mast cell tryptase and its inhibition.
J.Biol.Chem., 272, 1997
1LR7
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1lr7
CRYSTAL STRUCTURE OF FS1, THE HEPARIN-BINDING DOMAIN OF FOLLISTATIN, COMPLEXED WITH THE HEPARIN ANALOGUE SUCROSE OCTASULPHATE (SOS)
Descriptor:follistatin
Authors:Innis, C.A., Hyvonen, M.
Deposit date:2002-05-15
Release date:2003-07-29
Modification date:2009-02-24
Method:X-RAY DIFFRACTION (1.5 Å)
Cite:Crystal Structures of the Heparan Sulfate-binding Domain of Follistatin: Insights into ligand binding.
J.Biol.Chem., 278, 2003
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