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. 2013 Dec 2;8(12):e80562. doi: 10.1371/journal.pone.0080562

Table 2. Compressed sensing (CS), mutual information (MI), and ensemble classifier predictions of HIV-1 Env positions constituting bnMAb epitopes for PGT 127, 128, and 130.

bnMAb CS classifier MI classifier Ensemble classifier Experiment
nCS position residue nMI nCS position residue nMI
PGT-127 18 136 Ser 2 332 2 332 4 301
169 Lys 334 334 303
188 Asn 332
230 Asn 334
290 Arg
297 Thr
322 Ile
330 His
332 Asn
334 Asn
334 Ser
373 Thr
442 Glu
674 Asn
792 Ala
815 Val
817 Ala
843 Val
PGT-128 23 82 Arg 2 332 2 332 1 303
133 Lys 334 334
151 Gln
152 Glu
153 Gln
229 Arg
230 Asn
289 Val
297 Thr
306 Arg
323 Ile
326 Ile
332 Thr
334 Ser
347 Asp
373 Thr
442 Glu
500 Glu
520 Leu
754 Pro
792 Ala
815 Val
817 Thr
PGT-130 18 49 Asp 2 471 1 792 7 301
151 Asp 792 303
230 Asn 307
297 Thr 309
300 Ser 324
360 Val 325
373 Met 423
395 Cys
455 Glu
465 Thr
500 Glu
520 Leu
644 Asp
746 Ser
792 Ala
792 Leu
817 Thr
841 Leu

The experimentally identified positions are defined as those at which alanine point mutations were observed to increase the measured IC50 of the mutant by more than 30-fold relative to that of the wild type JR-CSF. Alanine scans were performed as part of the present work for PGT 143 and 145; data for PGT 121–135 were taken from Ref. [51].

Footnote: See footnote to Table 1.