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1YU0

Major Tropism Determinant P1 Variant

Summary for 1YU0
Entry DOI10.2210/pdb1yu0/pdb
Related1YU1 1YU2 1YU3 1YU4
DescriptorMajor Tropism Determinant (Mtd-P1), CALCIUM ION (3 entities in total)
Functional Keywordsc-type lectin, beta sandwich, beta prism, variability, diversity-generating retroelement, viral protein
Biological sourceBordetella phage BPP-1
Total number of polymer chains1
Total formula weight39637.64
Authors
McMahon, S.A.,Miller, J.L.,Lawton, J.A.,Ghosh, P. (deposition date: 2005-02-11, release date: 2005-09-20, Last modification date: 2024-02-14)
Primary citationMcMahon, S.A.,Miller, J.L.,Lawton, J.A.,Kerkow, D.E.,Hodes, A.,Marti-Renom, M.A.,Doulatov, S.,Narayanan, E.,Sali, A.,Miller, J.F.,Ghosh, P.
The C-type lectin fold as an evolutionary solution for massive sequence variation
Nat.Struct.Mol.Biol., 12:886-892, 2005
Cited by
PubMed Abstract: Only few instances are known of protein folds that tolerate massive sequence variation for the sake of binding diversity. The most extensively characterized is the immunoglobulin fold. We now add to this the C-type lectin (CLec) fold, as found in the major tropism determinant (Mtd), a retroelement-encoded receptor-binding protein of Bordetella bacteriophage. Variation in Mtd, with its approximately 10(13) possible sequences, enables phage adaptation to Bordetella spp. Mtd is an intertwined, pyramid-shaped trimer, with variable residues organized by its CLec fold into discrete receptor-binding sites. The CLec fold provides a highly static scaffold for combinatorial display of variable residues, probably reflecting a different evolutionary solution for balancing diversity against stability from that in the immunoglobulin fold. Mtd variants are biased toward the receptor pertactin, and there is evidence that the CLec fold is used broadly for sequence variation by related retroelements.
PubMed: 16170324
DOI: 10.1038/nsmb992
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.56 Å)
Structure validation

246031

数据于2025-12-10公开中

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