1YN3
| Crystal Structures of EAP Domains from Staphylococcus aureus Reveal an Unexpected Homology to Bacterial Superantigens | Descriptor: | truncated cell surface protein map-w | Authors: | Geisbrecht, B.V, Hamaoka, B.Y, Perman, B, Zemla, A, Leahy, D.J. | Deposit date: | 2005-01-23 | Release date: | 2005-03-01 | Last modified: | 2023-08-23 | Method: | X-RAY DIFFRACTION (1.35 Å) | Cite: | The Crystal Structures of EAP Domains from Staphylococcus aureus Reveal an Unexpected Homology to Bacterial Superantigens. J.Biol.Chem., 280, 2005
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1YN4
| Crystal Structures of EAP Domains from Staphylococcus aureus Reveal an Unexpected Homology to Bacterial Superantigens | Descriptor: | EapH1, ZINC ION | Authors: | Geisbrecht, B.V, Hamaoka, B.Y, Perman, B, Zemla, A, Leahy, D.J. | Deposit date: | 2005-01-23 | Release date: | 2005-03-01 | Last modified: | 2024-02-14 | Method: | X-RAY DIFFRACTION (1.8 Å) | Cite: | The Crystal Structures of EAP Domains from Staphylococcus aureus Reveal an Unexpected Homology to Bacterial Superantigens. J.Biol.Chem., 280, 2005
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1YN5
| Crystal Structures of EAP Domains from Staphylococcus aureus Reveal an Unexpected Homology to Bacterial Superantigens | Descriptor: | EapH2 | Authors: | Geisbrecht, B.V, Hamaoka, B.Y, Perman, B, Zemla, A, Leahy, D.J. | Deposit date: | 2005-01-23 | Release date: | 2005-03-01 | Last modified: | 2023-08-23 | Method: | X-RAY DIFFRACTION (2.2 Å) | Cite: | The Crystal Structures of EAP Domains from Staphylococcus aureus Reveal an Unexpected Homology to Bacterial Superantigens. J.Biol.Chem., 280, 2005
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7TE3
| Crystal Structure of a Double Loop Deletion Mutant in gC1qR/C1qBP/HABP-1 | Descriptor: | Complement component 1 Q subcomponent-binding protein, mitochondrial | Authors: | Geisbrecht, B.V. | Deposit date: | 2022-01-04 | Release date: | 2022-06-01 | Last modified: | 2023-10-25 | Method: | X-RAY DIFFRACTION (2.2 Å) | Cite: | gC1qR/C1qBP/HABP-1: Structural Analysis of the Trimeric Core Region, Interactions With a Novel Panel of Monoclonal Antibodies, and Their Influence on Binding to FXII. Front Immunol, 13, 2022
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3D5R
| Crystal Structure of Efb-C (N138A) / C3d Complex | Descriptor: | Complement C3, Fibrinogen-binding protein | Authors: | Geisbrecht, B.V. | Deposit date: | 2008-05-16 | Release date: | 2008-09-09 | Last modified: | 2024-10-16 | Method: | X-RAY DIFFRACTION (2.1 Å) | Cite: | Electrostatic contributions drive the interaction between Staphylococcus aureus protein Efb-C and its complement target C3d. Protein Sci., 17, 2008
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3D5S
| Crystal Structure of Efb-C (R131A) / C3d Complex | Descriptor: | Complement C3, Fibrinogen-binding protein | Authors: | Geisbrecht, B.V. | Deposit date: | 2008-05-16 | Release date: | 2008-09-16 | Last modified: | 2024-10-30 | Method: | X-RAY DIFFRACTION (2.3 Å) | Cite: | Electrostatic contributions drive the interaction between Staphylococcus aureus protein Efb-C and its complement target C3d. Protein Sci., 17, 2008
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8TYP
| Complement Protease C1s Inhibited by 6-(4-phenylpiperazin-1-yl)pyridine-3-carboximidamide | Descriptor: | 6-(4-phenylpiperazin-1-yl)pyridine-3-carboximidamide, Complement C1s subcomponent, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose | Authors: | Geisbrecht, B.V. | Deposit date: | 2023-08-25 | Release date: | 2023-11-29 | Last modified: | 2024-02-14 | Method: | X-RAY DIFFRACTION (1.8 Å) | Cite: | Inhibition of the C1s Protease and the Classical Complement Pathway by 6-(4-Phenylpiperazin-1-yl)Pyridine-3-Carboximidamide and Chemical Analogs. J Immunol., 212, 2024
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3KS2
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3L5N
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3L3O
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3NMS
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3OHX
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9BD0
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6D69
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8D7I
| Bifunctional Inhibition of Neutrophil Elastase and Cathepsin G by Eap1 from S. aureus | Descriptor: | Cathepsin G, C-terminal truncated form, Extracellular Adherence Protein, ... | Authors: | Gido, C.D, Herdendorf, T.J, Geisbrecht, B.V. | Deposit date: | 2022-06-07 | Release date: | 2023-06-14 | Last modified: | 2024-10-23 | Method: | X-RAY DIFFRACTION (3.63 Å) | Cite: | S. aureus Eap is a polyvalent inhibitor of neutrophil serine proteases. J.Biol.Chem., 300, 2024
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8D7K
| Bifunctional Inhibition of Neutrophil Elastase and Cathepsin G by Eap2 from S. aureus | Descriptor: | Cathepsin G, C-terminal truncated form, Extracellular Adherence Protein, ... | Authors: | Gido, C.D, Herdendorf, T.J, Geisbrecht, B.V. | Deposit date: | 2022-06-07 | Release date: | 2023-06-14 | Last modified: | 2024-10-23 | Method: | X-RAY DIFFRACTION (3.1 Å) | Cite: | S. aureus Eap is a polyvalent inhibitor of neutrophil serine proteases. J.Biol.Chem., 300, 2024
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2HHI
| The solution structure of antigen MPT64 from Mycobacterium tuberculosis defines a novel class of beta-grasp proteins | Descriptor: | Immunogenic protein MPT64 | Authors: | Wang, Z, Potter, B.M, Gray, A.M, Sacksteder, K.A, Geisbrecht, B.V, Laity, J.H. | Deposit date: | 2006-06-28 | Release date: | 2006-12-05 | Last modified: | 2011-07-13 | Method: | SOLUTION NMR | Cite: | The Solution Structure of Antigen MPT64 from Mycobacterium tuberculosis Defines a New Family of Beta-Grasp Proteins. J.Mol.Biol., 366, 2007
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6AZP
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6VTM
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9ATK
| BIFUNCTIONAL INHIBITION OF NEUTROPHIL ELASTASE AND CATHEPSIN G by Eap4 of S. aureus | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, Cathepsin-G, ... | Authors: | Mishra, N.B, Herdendorf, T.J, Geisbrecht, B.V. | Deposit date: | 2024-02-27 | Release date: | 2024-06-12 | Last modified: | 2024-10-23 | Method: | X-RAY DIFFRACTION (2.11 Å) | Cite: | S. aureus Eap is a polyvalent inhibitor of neutrophil serine proteases. J.Biol.Chem., 300, 2024
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9ASS
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9ASX
| BIFUNCTIONAL INHIBITION OF NEUTROPHIL ELASTASE AND CATHEPSIN G by Eap3 of S. aureus | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, Cathepsin-G, ... | Authors: | Mishra, N.B, Herdendorf, T.J, Geisbrecht, B.V. | Deposit date: | 2024-02-26 | Release date: | 2024-06-12 | Last modified: | 2024-10-23 | Method: | X-RAY DIFFRACTION (1.96 Å) | Cite: | S. aureus Eap is a polyvalent inhibitor of neutrophil serine proteases. J.Biol.Chem., 300, 2024
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9ATU
| Bifunctional Inhibition of Neutrophil Elastase by Eap4 from S. aureus | Descriptor: | 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, Extracellular Adherence Protein, Neutrophil elastase, ... | Authors: | Mishra, N.B, Herdendorf, T.J, Geisbrecht, B.V. | Deposit date: | 2024-02-27 | Release date: | 2024-06-12 | Last modified: | 2024-10-23 | Method: | X-RAY DIFFRACTION (2.05 Å) | Cite: | S. aureus Eap is a polyvalent inhibitor of neutrophil serine proteases. J.Biol.Chem., 300, 2024
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5JXU
| Structural basis for the catalytic activity of Thermomonospora curvata heme-containing DyP-type peroxidase. | Descriptor: | Dyp-type peroxidase family, PROTOPORPHYRIN IX CONTAINING FE | Authors: | Ramyar, K.X, Carlson, E.A, Li, P, Geisbrecht, B.V. | Deposit date: | 2016-05-13 | Release date: | 2016-10-19 | Last modified: | 2023-09-27 | Method: | X-RAY DIFFRACTION (1.751 Å) | Cite: | Identification of Surface-Exposed Protein Radicals and A Substrate Oxidation Site in A-Class Dye-Decolorizing Peroxidase from Thermomonospora curvata. ACS Catal, 6, 2016
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1FCH
| CRYSTAL STRUCTURE OF THE PTS1 COMPLEXED TO THE TPR REGION OF HUMAN PEX5 | Descriptor: | PEROXISOMAL TARGETING SIGNAL 1 RECEPTOR, PTS1-CONTAINING PEPTIDE | Authors: | Gatto Jr, G.J, Geisbrecht, B.V, Gould, S.J, Berg, J.M. | Deposit date: | 2000-07-18 | Release date: | 2000-12-06 | Last modified: | 2024-02-07 | Method: | X-RAY DIFFRACTION (2.2 Å) | Cite: | Peroxisomal targeting signal-1 recognition by the TPR domains of human PEX5. Nat.Struct.Biol., 7, 2000
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