Table 1 Assignment of the infrared bands distinguishable in the second derivatives of Clr-11/monomeric NKR-P1BSD/dimeric NKR-P1BSD/NKR-P1BWAG receptors FTIR spectra shown in Fig. 7 (ν corresponds to stretching, δ to bending, as to anti-symmetrical, and s to symmetrical vibrations).

From: Production of recombinant soluble dimeric C-type lectin-like receptors of rat natural killer cells

Frequency (cm−1)

Assignment

References

1227/—/—/—

β-sheet (amide III)/His

39,54,55,56

1242/1236/1236/1236

β-sheet (amide III)/Tyr–OH

39,54,55,56

1265/1246/1246/1244

coil (amide III)/Tyr–OH

39,54,55,56

1290/1292/1292/1288

β-turns (amide III)

54,55

1317/1315/1315/1315

α-helix (amide III)

54,55

1362/1350/1350/1342

Trp

39,56

1400/1400/1400/1398

Asp/Glu (νsCOO)

39,56

—/—/—/1419

Trp/Pro?

39,56

1439/1439/1439/1440

δCH2, Pro (νCN), His(δCH & δCN)

39,56

1456/1458/1460/1460

δCH2, δCH3/Tyr/Trp?

39,56

1489/—/1490/1489

Trp? (νCC ring & δCH)

39,56

—/1499/1500/1499

Phe/Tyr–O (νCC ring)?

39,56

1518/1519/1516/1516

Tyr–OH (νCC ring & δCH)

39,56

—/—/—/1533

amide II

40,56

—/—/—/1545

amide II

40,56

1549/1551/1550/—

amide II

40,56

—/—/—/1555

amide II

40,56

1568/—/1568/1568

Asp/Glu (νasCOO)

39,56

1597/1587/1583/1582

Tyr (νCC ring)

39,56

—/1601/—/—

Tyr–O (νCC ring)?

39,56

—/—/1610/1610

Tyr (νCC ring)

39,56

1637/1639/1639/1639

β-sheet (amide I)

40,57

1661/1652/1659/1657

α-helix/coil/turns (amide I)

40,57

1689/1688/1689/1689

β-sheet antiparallel/ turns (amide I)

40,57

—/—/1726/1726

Asp/Glu (νC=O)

39,54,56

—/1741/1745/1747

Asp/Glu (νC=O)

39,54,56