0 STRAND A (B.) (A.) (C.) (D.) (E.) (F.) (G.) (H.) O o 0 o 0 o (1.) 0 O 0 O HN" CHC-NHCHC NH CHANCIC NHẠCH CA NHẠCH CNCH

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0 STRAND A (B.) (A.) (C.) (D.) (E.) (F.) (G.) (H.) O o 0 o 0 o (1.) 0 O 0 O HN" CHC-NHCHC NH CHANCIC NHẠCH CA NHẠCH CNCH c NACHINE CIC 0 1 1 1 / 1 1 1 CH, CH, CH, CH 1 , CH2 CH CH, CH2 CH CH-CH, 1 1 1 1 / 1 1 1 co 1 с CH, CH CH SH с с CH, 1 / W 1 11 1 1 1 NH, HN CH с CH, CH, 0 0 HC CH CH 1 / | 1 I HC- NH O O HC CH // с 1 OH H2N NH2+ NHa* с 1 CH2 NH CH: 0 0 1 | 1 CH2 CH2 S с ! 1 1 OH CH2 CH2 CH2 SH CH2 OH HC CH 1 I 1 1 1 1 1 CH CH CH CH2 CH CH2 CH2 HCCH CH 1 1 1 1 HN+ CH -NH-CH=C NHẠCH CẨNHẠCH CẠNH CHỮ NHẠCH CẠNH-CH=C_NH_CH CNH-CH=C-0- 0 | 0 o o O O 0 o 0 O 0 (A.) (B.) (C.) (D.) (E.) (F.) (G.) (H.) (L.) STRAND B 1. Which three sidechain locations on the above polypeptide would be good places for hydrophobic pockets? 2. Which one of the sidechain locations on STRAND A would be a good place for attaching a heme group? 3. Which two sidechain locations on the above polypeptide would be good places for hydrogen bonding? 4. Which one of the sidechain locations on the above polypeptide would be a good location for an ion bridge? 5. Which sidechain location would be a good place for forming a covalent bond linking Strand A and Strand B? 6. Which two sidechain locations on the above polypeptide would be good places for forming a coordination bridge incorporating a metal ion? 7. What is the name of the amino acid occupying the “N-Terminal" of Strand A? 8. What is the name of the amino acid occupying the “C-Terminal” of Strand B? 9. Which one of the labeled positions on Strand A contains an amino acid side chain with a chiral carbon atom? 10. What is the name of the amino with the chiral carbon atom in question #9? 11. Which one of the labeled positions on Strand B could be used for the carbamination of a CO2 molecule? 12. What is the name of the amino acid identified in question #11?