data_2NH # _chem_comp.id 2NH _chem_comp.name "N-ACETYL-S-[(2E,6E)-3,7,11-TRIMETHYLDODECA-2,6,10-TRIENYL]-L-CYSTEINYL-D-VALYL-L-ISOLEUCYL-L-METHIONINE" _chem_comp.type NON-POLYMER _chem_comp.pdbx_type HETAIN _chem_comp.formula "C36 H62 N4 O6 S2" _chem_comp.mon_nstd_parent_comp_id ? _chem_comp.pdbx_synonyms ? _chem_comp.pdbx_formal_charge 0 _chem_comp.pdbx_initial_date 2003-04-25 _chem_comp.pdbx_modified_date 2011-06-04 _chem_comp.pdbx_ambiguous_flag N _chem_comp.pdbx_release_status REL _chem_comp.pdbx_replaced_by ? _chem_comp.pdbx_replaces ? _chem_comp.formula_weight 711.031 _chem_comp.one_letter_code ? _chem_comp.three_letter_code 2NH _chem_comp.pdbx_model_coordinates_details ? _chem_comp.pdbx_model_coordinates_missing_flag N _chem_comp.pdbx_ideal_coordinates_details ? _chem_comp.pdbx_ideal_coordinates_missing_flag N _chem_comp.pdbx_model_coordinates_db_code 1O1T _chem_comp.pdbx_subcomponent_list ? _chem_comp.pdbx_processing_site RCSB # loop_ _chem_comp_atom.comp_id _chem_comp_atom.atom_id _chem_comp_atom.alt_atom_id _chem_comp_atom.type_symbol _chem_comp_atom.charge _chem_comp_atom.pdbx_align _chem_comp_atom.pdbx_aromatic_flag _chem_comp_atom.pdbx_leaving_atom_flag _chem_comp_atom.pdbx_stereo_config _chem_comp_atom.model_Cartn_x _chem_comp_atom.model_Cartn_y _chem_comp_atom.model_Cartn_z _chem_comp_atom.pdbx_model_Cartn_x_ideal _chem_comp_atom.pdbx_model_Cartn_y_ideal _chem_comp_atom.pdbx_model_Cartn_z_ideal _chem_comp_atom.pdbx_component_atom_id _chem_comp_atom.pdbx_component_comp_id _chem_comp_atom.pdbx_ordinal 2NH CD1 CD1 C 0 1 N N N 183.579 125.167 32.944 -1.967 3.588 -4.398 CD1 2NH 1 2NH CG4 CG4 C 0 1 N N N 184.545 125.787 31.942 -0.968 2.532 -4.878 CG4 2NH 2 2NH CB4 CB4 C 0 1 N N S 185.731 124.884 31.599 -1.603 1.144 -4.773 CB4 2NH 3 2NH CG3 CG3 C 0 1 N N N 186.593 124.620 32.836 -1.981 0.865 -3.317 CG3 2NH 4 2NH CA4 CA4 C 0 1 N N S 186.604 125.505 30.464 -0.605 0.089 -5.253 CA4 2NH 5 2NH N3 N3 N 0 1 N N N 187.010 126.863 30.812 0.597 0.140 -4.418 N3 2NH 6 2NH C19 C19 C 0 1 N N N 188.282 127.240 30.790 0.678 -0.615 -3.305 C19 2NH 7 2NH O20 O20 O 0 1 N N N 189.210 126.473 30.528 -0.271 -1.283 -2.956 O20 2NH 8 2NH CA3 CA3 C 0 1 N N S 188.541 128.683 31.184 1.948 -0.629 -2.494 CA3 2NH 9 2NH N2 N2 N 0 1 N N N 189.539 128.771 32.260 1.636 -0.971 -1.104 N2 2NH 10 2NH C17 C17 C 0 1 N N N 189.214 128.569 33.540 2.400 -0.489 -0.104 C17 2NH 11 2NH O18 O18 O 0 1 N N N 188.065 128.339 33.922 3.346 0.227 -0.354 O18 2NH 12 2NH CA2 CA2 C 0 1 N N R 190.348 128.689 34.550 2.079 -0.841 1.325 CA2 2NH 13 2NH CB2 CB2 C 0 1 N N N 190.097 127.774 35.765 1.117 0.198 1.903 CB2 2NH 14 2NH SG SG S 0 1 N N N 191.563 127.288 36.702 0.731 -0.225 3.624 SG 2NH 15 2NH C C C 0 1 N N N 192.222 125.986 35.618 -0.393 1.136 4.039 C 2NH 16 2NH C2 C2 C 0 1 N N N 191.404 124.716 35.649 -0.856 0.988 5.465 C2 2NH 17 2NH C1 C1 C 0 1 N N N 190.502 124.380 34.705 -0.544 1.899 6.353 C1 2NH 18 2NH C4 C4 C 0 1 N N N 190.234 125.281 33.535 0.117 3.181 5.917 C4 2NH 19 2NH C3 C3 C 0 1 N N N 189.737 123.073 34.815 -0.847 1.665 7.811 C3 2NH 20 2NH C5 C5 C 0 1 N N N 189.719 122.359 33.467 0.346 0.976 8.475 C5 2NH 21 2NH C7 C7 C 0 1 N N N 188.428 121.546 33.390 0.043 0.742 9.933 C7 2NH 22 2NH C6 C6 C 0 1 N N N 187.942 121.109 32.228 0.182 -0.454 10.447 C6 2NH 23 2NH C8 C8 C 0 1 N N N 188.634 121.377 30.917 0.809 -1.556 9.633 C8 2NH 24 2NH C9 C9 C 0 1 N N N 186.643 120.307 32.201 -0.285 -0.728 11.853 C9 2NH 25 2NH C10 C10 C 0 1 N N N 185.471 121.190 31.849 -1.744 -1.189 11.825 C10 2NH 26 2NH C11 C11 C 0 1 N N N 184.191 120.368 31.907 -2.211 -1.464 13.231 C11 2NH 27 2NH C12 C12 C 0 1 N N N 183.136 120.585 31.105 -3.313 -0.911 13.674 C12 2NH 28 2NH C13 C13 C 0 1 N N N 183.127 121.684 30.072 -3.685 -1.035 15.129 C13 2NH 29 2NH C14 C14 C 0 1 N N N 181.901 119.691 31.240 -4.208 -0.150 12.730 C14 2NH 30 2NH N N N 0 1 N N N 190.543 130.074 34.965 3.314 -0.855 2.114 N 2NH 31 2NH C15 C15 C 0 1 N N N 191.756 130.632 34.981 4.062 0.260 2.213 C15 2NH 32 2NH CA CA C 0 1 N N N 191.828 132.078 35.437 5.332 0.246 3.024 CA 2NH 33 2NH O16 O16 O 0 1 N N N 192.791 130.027 34.651 3.714 1.276 1.650 O16 2NH 34 2NH CB3 CB3 C 0 1 N N N 188.931 129.523 29.929 2.910 -1.669 -3.071 CB3 2NH 35 2NH CG1 CG1 C 0 1 N N N 189.093 130.992 30.306 2.211 -3.028 -3.141 CG1 2NH 36 2NH CG2 CG2 C 0 1 N N N 190.200 128.989 29.285 3.338 -1.243 -4.477 CG2 2NH 37 2NH C22 C22 C 0 1 N N N 185.899 125.457 29.101 -0.233 0.364 -6.687 C22 2NH 38 2NH O23 O23 O 0 1 N N N 185.304 124.448 28.723 0.922 0.581 -6.983 O23 2NH 39 2NH N4 N4 N 0 1 N N N 186.005 126.567 28.373 -1.185 0.369 -7.641 N4 2NH 40 2NH CA5 CA5 C 0 1 N N S 185.426 126.727 27.038 -0.824 0.636 -9.035 CA5 2NH 41 2NH CB5 CB5 C 0 1 N N N 183.875 126.648 27.065 -1.790 -0.102 -9.963 CB5 2NH 42 2NH CG CG C 0 1 N N N 183.113 127.949 27.331 -1.706 -1.605 -9.694 CG 2NH 43 2NH SD SD S 0 1 N N N 181.303 127.844 27.226 -2.852 -2.482 -10.794 SD 2NH 44 2NH CE CE C 0 1 N N N 181.006 128.470 25.569 -2.548 -4.191 -10.269 CE 2NH 45 2NH C24 C24 C 0 1 N N N 185.923 128.046 26.413 -0.907 2.118 -9.300 C24 2NH 46 2NH OT1 OT1 O 0 1 N N N 185.642 128.267 25.224 -0.184 2.625 -10.125 OT1 2NH 47 2NH OT2 OT2 O 0 1 N N N 186.622 128.828 27.101 -1.783 2.873 -8.620 OT2 2NH 48 2NH HD11 1HD1 H 0 0 N N N 182.714 125.825 33.194 -1.514 4.576 -4.473 HD11 2NH 49 2NH HD12 2HD1 H 0 0 N N N 183.226 124.170 32.588 -2.862 3.550 -5.019 HD12 2NH 50 2NH HD13 3HD1 H 0 0 N N N 184.117 124.853 33.869 -2.235 3.389 -3.361 HD13 2NH 51 2NH HG41 1HG4 H 0 0 N N N 184.007 126.100 31.017 -0.699 2.731 -5.915 HG41 2NH 52 2NH HG42 2HG4 H 0 0 N N N 184.897 126.783 32.297 -0.073 2.570 -4.257 HG42 2NH 53 2NH HB4 HB4 H 0 1 N N N 185.318 123.913 31.236 -2.498 1.106 -5.394 HB4 2NH 54 2NH HG31 1HG3 H 0 0 N N N 187.457 123.961 32.586 -1.085 0.903 -2.696 HG31 2NH 55 2NH HG32 2HG3 H 0 0 N N N 186.924 125.569 33.317 -2.692 1.617 -2.975 HG32 2NH 56 2NH HG33 3HG3 H 0 0 N N N 185.989 124.205 33.677 -2.433 -0.123 -3.242 HG33 2NH 57 2NH HA4 HA4 H 0 1 N N N 187.523 124.882 30.367 -1.057 -0.899 -5.178 HA4 2NH 58 2NH HN3 HN3 H 0 1 N N N 186.360 127.598 31.089 1.336 0.717 -4.667 HN3 2NH 59 2NH HA3 HA3 H 0 1 N N N 187.601 129.119 31.595 2.413 0.355 -2.530 HA3 2NH 60 2NH HN2 HN2 H 0 1 N N N 190.524 128.987 32.108 0.880 -1.545 -0.904 HN2 2NH 61 2NH HA2 HA2 H 0 1 N N N 191.287 128.352 34.052 1.614 -1.826 1.361 HA2 2NH 62 2NH HB21 1HB2 H 0 0 N N N 189.350 128.244 36.446 1.582 1.183 1.867 HB21 2NH 63 2NH HB22 2HB2 H 0 0 N N N 189.532 126.866 35.446 0.198 0.208 1.316 HB22 2NH 64 2NH H1 1H H 0 1 N N N 192.336 126.359 34.573 0.128 2.086 3.923 H1 2NH 65 2NH H2A 2H H 0 1 N N N 193.290 125.775 35.855 -1.255 1.111 3.372 H2A 2NH 66 2NH H2 H2 H 0 1 N N N 191.472 123.954 36.444 -1.445 0.130 5.755 H2 2NH 67 2NH H41 1H4 H 0 1 N N N 189.488 125.003 32.754 0.163 3.213 4.828 H41 2NH 68 2NH H42 2H4 H 0 1 N N N 189.963 126.288 33.929 -0.460 4.030 6.281 H42 2NH 69 2NH H43 3H4 H 0 1 N N N 191.205 125.487 33.027 1.126 3.226 6.325 H43 2NH 70 2NH H31 1H3 H 0 1 N N N 190.138 122.421 35.626 -1.033 2.621 8.301 H31 2NH 71 2NH H32 2H3 H 0 1 N N N 188.709 123.224 35.220 -1.729 1.032 7.902 H32 2NH 72 2NH H51 1H5 H 0 1 N N N 189.844 123.055 32.605 0.532 0.020 7.985 H51 2NH 73 2NH H52 2H5 H 0 1 N N N 190.630 121.742 33.291 1.228 1.609 8.384 H52 2NH 74 2NH H7 H7 H 0 1 N N N 187.794 121.250 34.243 -0.287 1.562 10.554 H7 2NH 75 2NH H81 1H8 H 0 1 N N N 188.227 121.011 29.945 1.179 -1.147 8.693 H81 2NH 76 2NH H82 2H8 H 0 1 N N N 188.779 122.479 30.830 1.638 -1.993 10.190 H82 2NH 77 2NH H83 3H8 H 0 1 N N N 189.682 121.008 31.005 0.064 -2.324 9.427 H83 2NH 78 2NH H91 1H9 H 0 1 N N N 186.715 119.428 31.518 0.333 -1.509 12.296 H91 2NH 79 2NH H92 2H9 H 0 1 N N N 186.475 119.763 33.159 -0.203 0.180 12.448 H92 2NH 80 2NH H101 1H10 H 0 0 N N N 185.419 122.100 32.490 -2.363 -0.409 11.382 H101 2NH 81 2NH H102 2H10 H 0 0 N N N 185.603 121.698 30.865 -1.826 -2.099 11.230 H102 2NH 82 2NH H11 H11 H 0 1 N N N 184.009 119.529 32.600 -1.638 -2.117 13.872 H11 2NH 83 2NH H131 1H13 H 0 0 N N N 182.251 121.864 29.406 -4.626 -0.516 15.309 H131 2NH 84 2NH H132 2H13 H 0 0 N N N 183.359 122.641 30.593 -3.797 -2.089 15.387 H132 2NH 85 2NH H133 3H13 H 0 0 N N N 184.023 121.547 29.423 -2.902 -0.592 15.744 H133 2NH 86 2NH H141 1H14 H 0 0 N N N 181.025 119.871 30.574 -3.748 -0.116 11.742 H141 2NH 87 2NH H142 2H14 H 0 0 N N N 182.216 118.626 31.136 -5.174 -0.650 12.664 H142 2NH 88 2NH H143 3H14 H 0 0 N N N 181.555 119.714 32.300 -4.348 0.864 13.101 H143 2NH 89 2NH HN HN H 0 1 N N N 189.785 130.689 35.261 3.593 -1.668 2.564 HN 2NH 90 2NH HA1 1HA H 0 1 N N N 192.840 132.543 35.450 5.797 1.231 2.988 HA1 2NH 91 2NH HA2A 2HA H 0 0 N N N 191.136 132.700 34.823 5.100 -0.008 4.058 HA2A 2NH 92 2NH HA3A 3HA H 0 0 N N N 191.354 132.179 36.441 6.018 -0.494 2.613 HA3A 2NH 93 2NH HB3 HB3 H 0 1 N N N 188.108 129.435 29.181 3.789 -1.745 -2.432 HB3 2NH 94 2NH HG11 1HG1 H 0 0 N N N 189.371 131.592 29.408 2.896 -3.769 -3.552 HG11 2NH 95 2NH HG12 2HG1 H 0 0 N N N 188.183 131.394 30.810 1.906 -3.331 -2.139 HG12 2NH 96 2NH HG13 3HG1 H 0 0 N N N 189.819 131.129 31.140 1.331 -2.952 -3.781 HG13 2NH 97 2NH HG21 1HG2 H 0 0 N N N 190.478 129.589 28.387 2.453 -1.089 -5.095 HG21 2NH 98 2NH HG22 2HG2 H 0 0 N N N 191.038 128.931 30.017 3.906 -0.314 -4.419 HG22 2NH 99 2NH HG23 3HG2 H 0 0 N N N 190.111 127.904 29.041 3.959 -2.021 -4.920 HG23 2NH 100 2NH HN4 HN4 H 0 1 N N N 186.534 127.301 28.842 -2.110 0.195 -7.404 HN4 2NH 101 2NH HA5 HA5 H 0 1 N N N 185.768 125.879 26.399 0.192 0.290 -9.220 HA5 2NH 102 2NH HB51 1HB5 H 0 0 N N N 183.510 126.192 26.114 -2.807 0.243 -9.779 HB51 2NH 103 2NH HB52 2HB5 H 0 0 N N N 183.556 125.874 27.801 -1.521 0.096 -11.001 HB52 2NH 104 2NH HG1 1HG H 0 1 N N N 183.411 128.367 28.320 -0.689 -1.951 -9.879 HG1 2NH 105 2NH HG2 2HG H 0 1 N N N 183.486 128.752 26.653 -1.975 -1.805 -8.657 HG2 2NH 106 2NH HE1 1HE H 0 1 N N N 179.894 128.405 25.504 -3.176 -4.867 -10.849 HE1 2NH 107 2NH HE2 2HE H 0 1 N N N 181.437 129.475 25.355 -1.499 -4.440 -10.432 HE2 2NH 108 2NH HE3 3HE H 0 1 N N N 181.561 127.947 24.755 -2.785 -4.293 -9.210 HE3 2NH 109 2NH HT2 HT2 H 0 1 N N N 186.928 129.640 26.715 -1.836 3.823 -8.790 HT2 2NH 110 # loop_ _chem_comp_bond.comp_id _chem_comp_bond.atom_id_1 _chem_comp_bond.atom_id_2 _chem_comp_bond.value_order _chem_comp_bond.pdbx_aromatic_flag _chem_comp_bond.pdbx_stereo_config _chem_comp_bond.pdbx_ordinal 2NH CD1 CG4 SING N N 1 2NH CD1 HD11 SING N N 2 2NH CD1 HD12 SING N N 3 2NH CD1 HD13 SING N N 4 2NH CG4 CB4 SING N N 5 2NH CG4 HG41 SING N N 6 2NH CG4 HG42 SING N N 7 2NH CB4 CG3 SING N N 8 2NH CB4 CA4 SING N N 9 2NH CB4 HB4 SING N N 10 2NH CG3 HG31 SING N N 11 2NH CG3 HG32 SING N N 12 2NH CG3 HG33 SING N N 13 2NH CA4 N3 SING N N 14 2NH CA4 C22 SING N N 15 2NH CA4 HA4 SING N N 16 2NH N3 C19 SING N N 17 2NH N3 HN3 SING N N 18 2NH C19 O20 DOUB N N 19 2NH C19 CA3 SING N N 20 2NH CA3 N2 SING N N 21 2NH CA3 CB3 SING N N 22 2NH CA3 HA3 SING N N 23 2NH N2 C17 SING N N 24 2NH N2 HN2 SING N N 25 2NH C17 O18 DOUB N N 26 2NH C17 CA2 SING N N 27 2NH CA2 CB2 SING N N 28 2NH CA2 N SING N N 29 2NH CA2 HA2 SING N N 30 2NH CB2 SG SING N N 31 2NH CB2 HB21 SING N N 32 2NH CB2 HB22 SING N N 33 2NH SG C SING N N 34 2NH C C2 SING N N 35 2NH C H1 SING N N 36 2NH C H2A SING N N 37 2NH C2 C1 DOUB N E 38 2NH C2 H2 SING N N 39 2NH C1 C4 SING N N 40 2NH C1 C3 SING N N 41 2NH C4 H41 SING N N 42 2NH C4 H42 SING N N 43 2NH C4 H43 SING N N 44 2NH C3 C5 SING N N 45 2NH C3 H31 SING N N 46 2NH C3 H32 SING N N 47 2NH C5 C7 SING N N 48 2NH C5 H51 SING N N 49 2NH C5 H52 SING N N 50 2NH C7 C6 DOUB N E 51 2NH C7 H7 SING N N 52 2NH C6 C8 SING N N 53 2NH C6 C9 SING N N 54 2NH C8 H81 SING N N 55 2NH C8 H82 SING N N 56 2NH C8 H83 SING N N 57 2NH C9 C10 SING N N 58 2NH C9 H91 SING N N 59 2NH C9 H92 SING N N 60 2NH C10 C11 SING N N 61 2NH C10 H101 SING N N 62 2NH C10 H102 SING N N 63 2NH C11 C12 DOUB N N 64 2NH C11 H11 SING N N 65 2NH C12 C13 SING N N 66 2NH C12 C14 SING N N 67 2NH C13 H131 SING N N 68 2NH C13 H132 SING N N 69 2NH C13 H133 SING N N 70 2NH C14 H141 SING N N 71 2NH C14 H142 SING N N 72 2NH C14 H143 SING N N 73 2NH N C15 SING N N 74 2NH N HN SING N N 75 2NH C15 CA SING N N 76 2NH C15 O16 DOUB N N 77 2NH CA HA1 SING N N 78 2NH CA HA2A SING N N 79 2NH CA HA3A SING N N 80 2NH CB3 CG1 SING N N 81 2NH CB3 CG2 SING N N 82 2NH CB3 HB3 SING N N 83 2NH CG1 HG11 SING N N 84 2NH CG1 HG12 SING N N 85 2NH CG1 HG13 SING N N 86 2NH CG2 HG21 SING N N 87 2NH CG2 HG22 SING N N 88 2NH CG2 HG23 SING N N 89 2NH C22 O23 DOUB N N 90 2NH C22 N4 SING N N 91 2NH N4 CA5 SING N N 92 2NH N4 HN4 SING N N 93 2NH CA5 CB5 SING N N 94 2NH CA5 C24 SING N N 95 2NH CA5 HA5 SING N N 96 2NH CB5 CG SING N N 97 2NH CB5 HB51 SING N N 98 2NH CB5 HB52 SING N N 99 2NH CG SD SING N N 100 2NH CG HG1 SING N N 101 2NH CG HG2 SING N N 102 2NH SD CE SING N N 103 2NH CE HE1 SING N N 104 2NH CE HE2 SING N N 105 2NH CE HE3 SING N N 106 2NH C24 OT1 DOUB N N 107 2NH C24 OT2 SING N N 108 2NH OT2 HT2 SING N N 109 # loop_ _pdbx_chem_comp_descriptor.comp_id _pdbx_chem_comp_descriptor.type _pdbx_chem_comp_descriptor.program _pdbx_chem_comp_descriptor.program_version _pdbx_chem_comp_descriptor.descriptor 2NH SMILES ACDLabs 10.04 "O=C(NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)O)CCSC)C(C)CC)C(C)C)CSC\C=C(/C)CC\C=C(/C)CC\C=C(/C)C)C" 2NH SMILES_CANONICAL CACTVS 3.341 "CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CSC\C=C(/C)CC\C=C(/C)CCC=C(C)C)NC(C)=O)C(C)C)C(=O)N[C@@H](CCSC)C(O)=O" 2NH SMILES CACTVS 3.341 "CC[CH](C)[CH](NC(=O)[CH](NC(=O)[CH](CSCC=C(C)CCC=C(C)CCC=C(C)C)NC(C)=O)C(C)C)C(=O)N[CH](CCSC)C(O)=O" 2NH SMILES_CANONICAL "OpenEye OEToolkits" 1.5.0 "CC[C@H](C)[C@@H](C(=O)N[C@@H](CCSC)C(=O)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CSC\C=C(/C)\CC\C=C(/C)\CCC=C(C)C)NC(=O)C" 2NH SMILES "OpenEye OEToolkits" 1.5.0 "CCC(C)C(C(=O)NC(CCSC)C(=O)O)NC(=O)C(C(C)C)NC(=O)C(CSCC=C(C)CCC=C(C)CCC=C(C)C)NC(=O)C" 2NH InChI InChI 1.03 ;InChI=1S/C36H62N4O6S2/c1-11-27(8)32(35(44)38-29(36(45)46)19-20-47-10)40-34(43)31(24(4)5)39-33(42)30(37-28(9)41)22-48-21-18-26(7)17-13-16-25(6)15-12-14-23(2)3/h14,16,18,24,27,29-32H,11-13,15,17,19-22H2,1-10H3,(H,37,41)(H,38,44)(H,39,42)(H,40,43)(H,45,46)/b25-16+,26-18+/t27-,29-,30-,31-,32-/m0/s1 ; 2NH InChIKey InChI 1.03 LZZSZMJTHYOSLN-UNXIWMFYSA-N # loop_ _pdbx_chem_comp_identifier.comp_id _pdbx_chem_comp_identifier.type _pdbx_chem_comp_identifier.program _pdbx_chem_comp_identifier.program_version _pdbx_chem_comp_identifier.identifier 2NH "SYSTEMATIC NAME" ACDLabs 10.04 "N-acetyl-S-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-L-cysteinyl-L-valyl-L-isoleucyl-L-methionine" 2NH "SYSTEMATIC NAME" "OpenEye OEToolkits" 1.5.0 "(2S)-2-[[(2S,3S)-2-[[(2S)-2-[[(2R)-2-acetamido-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanyl-propanoyl]amino]-3-methyl-butanoyl]amino]-3-methyl-pentanoyl]amino]-4-methylsulfanyl-butanoic acid" # loop_ _pdbx_chem_comp_audit.comp_id _pdbx_chem_comp_audit.action_type _pdbx_chem_comp_audit.date _pdbx_chem_comp_audit.processing_site 2NH "Create component" 2003-04-25 RCSB 2NH "Modify descriptor" 2011-06-04 RCSB #