NMR Restraints Grid |
Result table
image | mrblock_id | pdb_id | bmrb_id | cing | stage | program | type |
461645 | 2e7h | 11227 | cing | 1-original | MR format | comment |
*HEADER TRANSFERASE, SIGNALING PROTEIN 10-JAN-07 2E7H *TITLE SOLUTION STRUCTURE OF THE SECOND FN3 DOMAIN FROM HUMAN *TITLE 2 EPHRIN TYPE-B RECEPTOR 4 *COMPND MOL_ID: 1; *COMPND 2 MOLECULE: EPHRIN TYPE-B RECEPTOR 4; *COMPND 3 CHAIN: A; *COMPND 4 FRAGMENT: FN3 DOMAIN; *COMPND 5 SYNONYM: TYROSINE-PROTEIN KINASE RECEPTOR HTK; *COMPND 6 EC: 2.7.10.1; *COMPND 7 ENGINEERED: YES *SOURCE MOL_ID: 1; *SOURCE 2 ORGANISM_SCIENTIFIC: HOMO SAPIENS; *SOURCE 3 ORGANISM_COMMON: HUMAN; *SOURCE 4 ORGANISM_TAXID: 9606; *SOURCE 5 GENE: EPHB4, HTK; *SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID; *SOURCE 7 EXPRESSION_SYSTEM_PLASMID: P050919-21; *SOURCE 8 OTHER_DETAILS: CELL FREE PROTEIN SYNTHESIS *KEYWDS FN3 DOMAIN, EPHRIN TYPE-B RECEPTOR 4 PRECURSOR, TYROSINE- *KEYWDS 2 PROTEIN KINASE RECEPTOR HTK, STRUCTURAL GENOMICS, NPPSFA, *KEYWDS 3 NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL *KEYWDS 4 ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, *KEYWDS 5 RSGI, TRANSFERASE, SIGNALING PROTEIN *EXPDTA SOLUTION NMR *NUMMDL 20 *AUTHOR X.R.QIN, F.HAYASHI, S.YOKOYAMA, RIKEN STRUCTURAL *AUTHOR 2 GENOMICS/PROTEOMICS INITIATIVE (RSGI) *REVDAT 1 12-MAY-09 2E7H 0 ************************************************************** During the CYANA calculations automatic implicit swapping of restraints involving diastereotopic substitutents was applied for prochrial groups without stereospecific assignment. Diastereotopic substitents were swapped individually in each conformer to calculate the minimal target function and restraint violations. The optimal swapping for a given prochiral group may differ among the 20 conformers that represent the solution structure. The swapping is therefore performed implicitly in the program and is not reflected in the distance restraint file deposited in the PDB. **************************************************************
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