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Yorodumi- PDB-2hbd: HIGH RESOLUTION X-RAY STRUCTURES OF MYOGLOBIN-AND HEMOGLOBIN-ALKY... -
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-Basic information
Entry | Database: PDB / ID: 2hbd | ||||||
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Title | HIGH RESOLUTION X-RAY STRUCTURES OF MYOGLOBIN-AND HEMOGLOBIN-ALKYL ISOCYANIDE COMPLEXES | ||||||
Components |
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Keywords | OXYGEN TRANSPORT | ||||||
Function / homology | Function and homology information nitric oxide transport / hemoglobin alpha binding / cellular oxidant detoxification / hemoglobin binding / haptoglobin-hemoglobin complex / renal absorption / organic acid binding / hemoglobin complex / oxygen transport / Scavenging of heme from plasma ...nitric oxide transport / hemoglobin alpha binding / cellular oxidant detoxification / hemoglobin binding / haptoglobin-hemoglobin complex / renal absorption / organic acid binding / hemoglobin complex / oxygen transport / Scavenging of heme from plasma / endocytic vesicle lumen / blood vessel diameter maintenance / hydrogen peroxide catabolic process / oxygen carrier activity / carbon dioxide transport / Late endosomal microautophagy / Heme signaling / Erythrocytes take up oxygen and release carbon dioxide / Erythrocytes take up carbon dioxide and release oxygen / response to hydrogen peroxide / Cytoprotection by HMOX1 / platelet aggregation / oxygen binding / regulation of blood pressure / Chaperone Mediated Autophagy / positive regulation of nitric oxide biosynthetic process / tertiary granule lumen / Factors involved in megakaryocyte development and platelet production / blood microparticle / ficolin-1-rich granule lumen / iron ion binding / heme binding / Neutrophil degranulation / extracellular space / extracellular exosome / extracellular region / membrane / metal ion binding / cytosol Similarity search - Function | ||||||
Biological species | Homo sapiens (human) | ||||||
Method | X-RAY DIFFRACTION / Resolution: 2.2 Å | ||||||
Authors | Johnson, K.A. / Olson, J.S. / Phillips Jr., G.N. | ||||||
Citation | Journal: Thesis / Year: 1993 Title: High Resolution X-Ray Structures of Myoglobin-and Hemoglobin-Alkyl Isocyanide Complexes Authors: Johnson, K.A. #1: Journal: J.Mol.Biol. / Year: 1989 Title: Structure of Myoglobin-Ethyl Isocyanide: Histidine as a Swinging Door for Ligand Entry Authors: Johnson, K.A. / Olson, J.S. / Phillips Jr., G.N. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 2hbd.cif.gz | 70.2 KB | Display | PDBx/mmCIF format |
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PDB format | pdb2hbd.ent.gz | 53.7 KB | Display | PDB format |
PDBx/mmJSON format | 2hbd.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 2hbd_validation.pdf.gz | 547.2 KB | Display | wwPDB validaton report |
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Full document | 2hbd_full_validation.pdf.gz | 560.7 KB | Display | |
Data in XML | 2hbd_validation.xml.gz | 9.9 KB | Display | |
Data in CIF | 2hbd_validation.cif.gz | 13.6 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/hb/2hbd ftp://data.pdbj.org/pub/pdb/validation_reports/hb/2hbd | HTTPS FTP |
-Related structure data
Similar structure data |
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-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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-Components
#1: Protein | Mass: 15150.353 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Organ: SEED / References: UniProt: P69905 | ||||
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#2: Protein | Mass: 15890.198 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Organ: SEED / References: UniProt: P68871 | ||||
#3: Chemical | #4: Chemical | #5: Water | ChemComp-HOH / | |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION |
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-Sample preparation
Crystal | Density Matthews: 2.28 Å3/Da / Density % sol: 46.03 % |
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-Processing
Software |
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Refinement | Resolution: 2.2→5 Å / Rfactor Rwork: 0.176 / Rfactor obs: 0.176 / σ(F): 0 Details: REFINEMENT. THE STARTING MODEL WAS THE ETHYL ISOCYANIDE - HEMOGLOBIN (1HBC) COMPLEX WITH THE LIGAND REMOVED AND THE METHYL ISOCYANIDE LIGAND MODELED INTO INITIAL DIFFERENCE MAP (FO-FC) ...Details: REFINEMENT. THE STARTING MODEL WAS THE ETHYL ISOCYANIDE - HEMOGLOBIN (1HBC) COMPLEX WITH THE LIGAND REMOVED AND THE METHYL ISOCYANIDE LIGAND MODELED INTO INITIAL DIFFERENCE MAP (FO-FC) ELECTRON DENSITY. THE PROGRAM X-PLOR WAS USED TO ACHIEVE A FINAL CONVENTIONAL R- FACTOR OF 17.6%. THE REFINEMENT PROCESS INCLUDED SIMULATED ANNEALING FOLLOWED BY POSITION AND TEMPERATURE FACTOR REFINEMENT. AN ITERATIVE PROCESS OF MANUAL REFITTING OF SIDE CHAINS AND PLACEMENT OF WATERS WAS PERFORMED UNTIL THE R-FACTOR CONVERGED. THE WEIGHTING OF PSEUDO-ENERGY X-RAY TERM WAS ADJUSTED TO GIVE A BOND RMS OF 0.020 ANGSTROMS IN THE LAST FEW STEPS OF POSITIONAL REFINEMENT. WATERS (N=109) WERE RETAINED FROM THE STARTING STRUCTURE OF OXYHEMOGLOBIN (1HHO). ADDITIONAL WATERS WERE ADDED IF THEY LAY IN 3.5 - 4.O SIGMA PEAKS IN FO-FC ELECTRON DENSITY MAPS AND 1 SIGMA PEAKS IN 2FO-FC MAPS. CONCURRENTLY, A WATER WOULD BE DELETED IF ITS OCCUPANCY (Q) AND TEMPERATURE FACTOR (B) COMBINED TO MAKE THE VALUE (Q*EXP(- B/36)*100%) FALL BELOW 10%. A PEAK NUMBER OF 104 WATERS WAS REACHED. THIS WAS REDUCED TO 66 WATERS OVER THE LAST FEW REFINEMENT CYCLES BY DELETING WATERS WHICH FELL BELOW A 20% THRESHOLD. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refinement step | Cycle: LAST / Resolution: 2.2→5 Å
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Refine LS restraints |
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