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4AT6

Fab fragment of antiporphyrin antibody 14H7

Summary for 4AT6
Entry DOI10.2210/pdb4at6/pdb
DescriptorFAB 14H7 HEAVY CHAIN, FAB 14H7 LIGHT CHAIN (3 entities in total)
Functional Keywordsimmune system, metalloporphyrin, catalytic antibody, peroxidase
Biological sourceMUS MUSCULUS (HOUSE MOUSE)
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Total number of polymer chains16
Total formula weight365085.94
Authors
Golinelli-Pimpaneau, B.,Mahy, J.P. (deposition date: 2012-05-04, release date: 2012-10-31, Last modification date: 2023-12-20)
Primary citationMunoz Robles, V.,Marechal, J.,Bahloul, A.,Sari, M.,Mahy, J.,Golinelli-Pimpaneau, B.
Crystal Structure of Two Anti-Porphyrin Antibodies with Peroxidase Activity.
Plos One, 7:51128-, 2012
Cited by
PubMed Abstract: We report the crystal structures at 2.05 and 2.45 Å resolution of two antibodies, 13G10 and 14H7, directed against an iron(III)-αααβ-carboxyphenylporphyrin, which display some peroxidase activity. Although these two antibodies differ by only one amino acid in their variable λ-light chain and display 86% sequence identity in their variable heavy chain, their complementary determining regions (CDR) CDRH1 and CDRH3 adopt very different conformations. The presence of Met or Leu residues at positions preceding residue H101 in CDRH3 in 13G10 and 14H7, respectively, yields to shallow combining sites pockets with different shapes that are mainly hydrophobic. The hapten and other carboxyphenyl-derivatized iron(III)-porphyrins have been modeled in the active sites of both antibodies using protein ligand docking with the program GOLD. The hapten is maintained in the antibody pockets of 13G10 and 14H7 by a strong network of hydrogen bonds with two or three carboxylates of the carboxyphenyl substituents of the porphyrin, respectively, as well as numerous stacking and van der Waals interactions with the very hydrophobic CDRH3. However, no amino acid residue was found to chelate the iron. Modeling also allows us to rationalize the recognition of alternative porphyrinic cofactors by the 13G10 and 14H7 antibodies and the effect of imidazole binding on the peroxidase activity of the 13G10/porphyrin complexes.
PubMed: 23240001
DOI: 10.1371/JOURNAL.PONE.0051128
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.549 Å)
Structure validation

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건을2024-11-06부터공개중

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