A family of very long coiled-coil proteins, likely performing cytoskeletal functions.. Two varieties have evolved, one with an N-terminal FYVE domain (Non-TM) and another with a C-terminal PDZ domain (might be TM)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0000795 | synaptonemal complex | 3 | 1 |
GO:0099086 | synaptonemal structure | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4H3R9
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0006810 | transport | 3 | 5 |
GO:0006869 | lipid transport | 5 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0042157 | lipoprotein metabolic process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0071702 | organic substance transport | 4 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007130 | synaptonemal complex assembly | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 1 |
GO:0070193 | synaptonemal complex organization | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 5 |
GO:0008289 | lipid binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043169 | cation binding | 3 | 3 |
GO:0046872 | metal ion binding | 4 | 3 |
GO:0003774 | cytoskeletal motor activity | 1 | 1 |
GO:0003777 | microtubule motor activity | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 904 | 906 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 960 | 962 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 904 | 906 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 960 | 962 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 1090 | 1094 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 963 | 967 | PF00082 | 0.498 |
DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.334 |
DEG_APCC_DBOX_1 | 923 | 931 | PF00400 | 0.298 |
DEG_APCC_DBOX_1 | 962 | 970 | PF00400 | 0.303 |
DEG_Nend_Nbox_1 | 1 | 2 | PF02207 | 0.576 |
DEG_SPOP_SBC_1 | 1121 | 1125 | PF00917 | 0.639 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.681 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.687 |
DOC_CKS1_1 | 40 | 45 | PF01111 | 0.541 |
DOC_MAPK_gen_1 | 1090 | 1099 | PF00069 | 0.492 |
DOC_USP7_MATH_1 | 1121 | 1125 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 1126 | 1130 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.865 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 1122 | 1127 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 1155 | 1160 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 1162 | 1167 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 1109 | 1115 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 1120 | 1126 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 174 | 183 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 252 | 261 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 291 | 300 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 330 | 339 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 369 | 378 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 408 | 417 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 447 | 456 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 486 | 495 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 525 | 534 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 564 | 573 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 603 | 612 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 642 | 651 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 681 | 690 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 720 | 729 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 759 | 768 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 798 | 807 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 837 | 846 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 876 | 885 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 904 | 910 | PF00244 | 0.378 |
LIG_Actin_WH2_2 | 1075 | 1092 | PF00022 | 0.547 |
LIG_Actin_WH2_2 | 92 | 109 | PF00022 | 0.331 |
LIG_Actin_WH2_2 | 948 | 965 | PF00022 | 0.298 |
LIG_FHA_1 | 1006 | 1012 | PF00498 | 0.318 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.362 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.627 |
LIG_FHA_2 | 1028 | 1034 | PF00498 | 0.564 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.314 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.314 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.314 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.314 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.314 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.277 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.277 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.277 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.314 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.277 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.314 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.616 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.314 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.314 |
LIG_FHA_2 | 666 | 672 | PF00498 | 0.314 |
LIG_FHA_2 | 705 | 711 | PF00498 | 0.314 |
LIG_FHA_2 | 744 | 750 | PF00498 | 0.314 |
LIG_FHA_2 | 783 | 789 | PF00498 | 0.314 |
LIG_FHA_2 | 822 | 828 | PF00498 | 0.314 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.364 |
LIG_LIR_Gen_1 | 1104 | 1114 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 1104 | 1110 | PF02991 | 0.528 |
LIG_PCNA_yPIPBox_3 | 892 | 903 | PF02747 | 0.298 |
LIG_SH2_STAP1 | 35 | 39 | PF00017 | 0.655 |
LIG_SH3_3 | 1115 | 1121 | PF00018 | 0.666 |
LIG_SH3_3 | 1138 | 1144 | PF00018 | 0.600 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.704 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.581 |
LIG_SH3_3 | 920 | 926 | PF00018 | 0.256 |
LIG_SUMO_SIM_par_1 | 1095 | 1101 | PF11976 | 0.494 |
LIG_TRAF2_1 | 1007 | 1010 | PF00917 | 0.338 |
LIG_TRAF2_1 | 1018 | 1021 | PF00917 | 0.557 |
LIG_TRAF2_1 | 1064 | 1067 | PF00917 | 0.582 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.725 |
MOD_CK1_1 | 1105 | 1111 | PF00069 | 0.630 |
MOD_CK1_1 | 1124 | 1130 | PF00069 | 0.589 |
MOD_CK1_1 | 1132 | 1138 | PF00069 | 0.590 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.640 |
MOD_CK2_1 | 1004 | 1010 | PF00069 | 0.253 |
MOD_CK2_1 | 1027 | 1033 | PF00069 | 0.582 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.298 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.304 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.250 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.301 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.237 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.298 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.231 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.304 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.250 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.301 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.237 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.259 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.235 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.259 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.235 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.259 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.235 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.298 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.218 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.271 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.283 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.301 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.237 |
MOD_CK2_1 | 587 | 593 | PF00069 | 0.298 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.231 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.302 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.218 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.304 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.250 |
MOD_CK2_1 | 704 | 710 | PF00069 | 0.301 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.237 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.301 |
MOD_CK2_1 | 759 | 765 | PF00069 | 0.237 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.301 |
MOD_CK2_1 | 798 | 804 | PF00069 | 0.237 |
MOD_CK2_1 | 821 | 827 | PF00069 | 0.298 |
MOD_CK2_1 | 837 | 843 | PF00069 | 0.314 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.301 |
MOD_CK2_1 | 876 | 882 | PF00069 | 0.336 |
MOD_CK2_1 | 985 | 991 | PF00069 | 0.307 |
MOD_GlcNHglycan | 1069 | 1072 | PF01048 | 0.488 |
MOD_GlcNHglycan | 1110 | 1113 | PF01048 | 0.698 |
MOD_GlcNHglycan | 1128 | 1131 | PF01048 | 0.563 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.737 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.472 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.634 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.737 |
MOD_GSK3_1 | 1097 | 1104 | PF00069 | 0.579 |
MOD_GSK3_1 | 1120 | 1127 | PF00069 | 0.673 |
MOD_GSK3_1 | 1129 | 1136 | PF00069 | 0.658 |
MOD_GSK3_1 | 1162 | 1169 | PF00069 | 0.583 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.298 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.298 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.298 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.732 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.298 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.298 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.653 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.256 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.256 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.256 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.256 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.298 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.298 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.298 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.298 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.298 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.298 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.298 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.298 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.298 |
MOD_GSK3_1 | 872 | 879 | PF00069 | 0.300 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.333 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.591 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.504 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.688 |
MOD_NEK2_1 | 1013 | 1018 | PF00069 | 0.554 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.350 |
MOD_NEK2_1 | 1110 | 1115 | PF00069 | 0.739 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.629 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.374 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.730 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.632 |
MOD_PKA_2 | 1067 | 1073 | PF00069 | 0.496 |
MOD_PKA_2 | 1108 | 1114 | PF00069 | 0.648 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.350 |
MOD_Plk_1 | 1132 | 1138 | PF00069 | 0.633 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.298 |
MOD_Plk_2-3 | 914 | 920 | PF00069 | 0.298 |
MOD_Plk_4 | 1102 | 1108 | PF00069 | 0.597 |
MOD_Plk_4 | 1133 | 1139 | PF00069 | 0.634 |
MOD_Plk_4 | 985 | 991 | PF00069 | 0.298 |
MOD_ProDKin_1 | 1122 | 1128 | PF00069 | 0.645 |
MOD_ProDKin_1 | 1155 | 1161 | PF00069 | 0.585 |
MOD_ProDKin_1 | 1162 | 1168 | PF00069 | 0.564 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.658 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.564 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.682 |
MOD_SUMO_for_1 | 1092 | 1095 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 80 | 85 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 942 | 950 | PF00179 | 0.339 |
TRG_DiLeu_BaEn_1 | 1035 | 1040 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_4 | 101 | 107 | PF01217 | 0.360 |
TRG_DiLeu_BaEn_4 | 957 | 963 | PF01217 | 0.318 |
TRG_ER_diArg_1 | 1000 | 1003 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 1014 | 1017 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 903 | 905 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 960 | 963 | PF00400 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 1017 | 1021 | PF00026 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 1052 | 1056 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 1059 | 1063 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 56 | 61 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 953 | 957 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 960 | 964 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 992 | 996 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H530 | Leishmania donovani | 61% | 74% |
A0A3S7X6W4 | Leishmania donovani | 33% | 100% |
A4H3J9 | Leishmania braziliensis | 94% | 81% |
C9ZSW5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AJR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 85% |
E9AKC9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q54G05 | Dictyostelium discoideum | 21% | 79% |