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: 20 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000139 | Golgi membrane | 5 | 12 |
GO:0005840 | ribosome | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0030117 | membrane coat | 3 | 12 |
GO:0030120 | vesicle coat | 4 | 12 |
GO:0030126 | COPI vesicle coat | 5 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0098588 | bounding membrane of organelle | 4 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
Related structures:
AlphaFold database: A4HBF3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0048193 | Golgi vesicle transport | 5 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 1 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 844 | 848 | PF00656 | 0.501 |
CLV_C14_Caspase3-7 | 898 | 902 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 1101 | 1103 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.284 |
CLV_PCSK_KEX2_1 | 1101 | 1103 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.207 |
CLV_PCSK_PC1ET2_1 | 499 | 501 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 857 | 859 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 1009 | 1013 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 1091 | 1095 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 1101 | 1105 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.266 |
DEG_APCC_DBOX_1 | 1172 | 1180 | PF00400 | 0.407 |
DEG_APCC_DBOX_1 | 574 | 582 | PF00400 | 0.524 |
DEG_APCC_DBOX_1 | 594 | 602 | PF00400 | 0.372 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.427 |
DEG_SCF_SKP2-CKS1_1 | 928 | 935 | PF00560 | 0.524 |
DOC_CYCLIN_RxL_1 | 1098 | 1107 | PF00134 | 0.467 |
DOC_CYCLIN_RxL_1 | 496 | 506 | PF00134 | 0.487 |
DOC_CYCLIN_RxL_1 | 81 | 90 | PF00134 | 0.304 |
DOC_MAPK_gen_1 | 1070 | 1080 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 168 | 176 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 575 | 583 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 8 | 17 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 988 | 997 | PF00069 | 0.568 |
DOC_MAPK_HePTP_8 | 573 | 585 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 1009 | 1016 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 1041 | 1049 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 1073 | 1080 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 576 | 585 | PF00069 | 0.568 |
DOC_MAPK_NFAT4_5 | 1009 | 1017 | PF00069 | 0.524 |
DOC_MAPK_NFAT4_5 | 1073 | 1081 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 195 | 202 | PF00149 | 0.466 |
DOC_PP4_FxxP_1 | 351 | 354 | PF00568 | 0.568 |
DOC_PP4_FxxP_1 | 440 | 443 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 1168 | 1172 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 881 | 885 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 911 | 915 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 944 | 948 | PF00917 | 0.457 |
DOC_USP7_UBL2_3 | 1149 | 1153 | PF12436 | 0.568 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.568 |
DOC_USP7_UBL2_3 | 481 | 485 | PF12436 | 0.491 |
DOC_WW_Pin1_4 | 1154 | 1159 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 1163 | 1168 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 929 | 934 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 1050 | 1057 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 1073 | 1079 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 1160 | 1164 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 221 | 226 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 97 | 101 | PF00244 | 0.468 |
LIG_Actin_WH2_2 | 975 | 992 | PF00022 | 0.491 |
LIG_APCC_ABBA_1 | 143 | 148 | PF00400 | 0.568 |
LIG_BIR_III_4 | 724 | 728 | PF00653 | 0.407 |
LIG_BIR_III_4 | 875 | 879 | PF00653 | 0.461 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.497 |
LIG_BRCT_BRCA1_1 | 232 | 236 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 436 | 440 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 515 | 519 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 955 | 959 | PF00533 | 0.408 |
LIG_CaM_IQ_9 | 446 | 461 | PF13499 | 0.524 |
LIG_EH_1 | 1138 | 1142 | PF12763 | 0.466 |
LIG_eIF4E_1 | 249 | 255 | PF01652 | 0.509 |
LIG_eIF4E_1 | 686 | 692 | PF01652 | 0.568 |
LIG_FHA_1 | 1038 | 1044 | PF00498 | 0.566 |
LIG_FHA_1 | 1075 | 1081 | PF00498 | 0.492 |
LIG_FHA_1 | 1126 | 1132 | PF00498 | 0.533 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.491 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.466 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.568 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.427 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.429 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.480 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.471 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.466 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.588 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.544 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.516 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.596 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.536 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.498 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.594 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.568 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.568 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.554 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.539 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.496 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.406 |
LIG_FHA_2 | 1026 | 1032 | PF00498 | 0.481 |
LIG_FHA_2 | 1093 | 1099 | PF00498 | 0.524 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.494 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.533 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.479 |
LIG_FHA_2 | 896 | 902 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 437 | 443 | PF02991 | 0.568 |
LIG_LIR_Apic_2 | 883 | 889 | PF02991 | 0.557 |
LIG_LIR_Apic_2 | 900 | 906 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 480 | 490 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 797 | 807 | PF02991 | 0.475 |
LIG_LIR_LC3C_4 | 148 | 151 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 1006 | 1011 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 593 | 597 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 659 | 663 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 668 | 673 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 787 | 793 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 797 | 803 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 891 | 895 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 980 | 984 | PF02991 | 0.466 |
LIG_LYPXL_yS_3 | 892 | 895 | PF13949 | 0.407 |
LIG_NRBOX | 690 | 696 | PF00104 | 0.568 |
LIG_Pex14_1 | 479 | 483 | PF04695 | 0.466 |
LIG_Pex14_1 | 899 | 903 | PF04695 | 0.491 |
LIG_PTB_Apo_2 | 549 | 556 | PF02174 | 0.491 |
LIG_PTB_Phospho_1 | 549 | 555 | PF10480 | 0.491 |
LIG_SH2_CRK | 1152 | 1156 | PF00017 | 0.568 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.496 |
LIG_SH2_CRK | 903 | 907 | PF00017 | 0.506 |
LIG_SH2_GRB2like | 721 | 724 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 903 | 907 | PF00017 | 0.491 |
LIG_SH2_PTP2 | 410 | 413 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 886 | 889 | PF00017 | 0.477 |
LIG_SH2_SRC | 410 | 413 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 1039 | 1043 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.568 |
LIG_SH2_STAT3 | 326 | 329 | PF00017 | 0.452 |
LIG_SH2_STAT3 | 937 | 940 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 1039 | 1042 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 1065 | 1068 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 1163 | 1166 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 721 | 724 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 886 | 889 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 903 | 906 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.466 |
LIG_SH2_STAT6 | 992 | 996 | PF00017 | 0.568 |
LIG_SH3_3 | 1152 | 1158 | PF00018 | 0.518 |
LIG_SH3_3 | 1164 | 1170 | PF00018 | 0.434 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.514 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.568 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.403 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.539 |
LIG_SH3_3 | 930 | 936 | PF00018 | 0.477 |
LIG_SH3_3 | 970 | 976 | PF00018 | 0.500 |
LIG_SH3_4 | 1149 | 1156 | PF00018 | 0.568 |
LIG_SH3_4 | 424 | 431 | PF00018 | 0.407 |
LIG_SUMO_SIM_anti_2 | 484 | 490 | PF11976 | 0.564 |
LIG_SUMO_SIM_anti_2 | 493 | 498 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 1076 | 1081 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 492 | 498 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 689 | 696 | PF11976 | 0.494 |
LIG_TRFH_1 | 1163 | 1167 | PF08558 | 0.512 |
LIG_TYR_ITIM | 408 | 413 | PF00017 | 0.524 |
LIG_TYR_ITIM | 534 | 539 | PF00017 | 0.496 |
LIG_UBA3_1 | 597 | 605 | PF00899 | 0.568 |
LIG_WRC_WIRS_1 | 274 | 279 | PF05994 | 0.539 |
MOD_CDC14_SPxK_1 | 1157 | 1160 | PF00782 | 0.506 |
MOD_CDK_SPxK_1 | 1154 | 1160 | PF00069 | 0.524 |
MOD_CDK_SPxK_1 | 929 | 935 | PF00069 | 0.524 |
MOD_CK1_1 | 1015 | 1021 | PF00069 | 0.524 |
MOD_CK1_1 | 1053 | 1059 | PF00069 | 0.496 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.397 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.555 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.491 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.515 |
MOD_CK1_1 | 798 | 804 | PF00069 | 0.434 |
MOD_CK1_1 | 914 | 920 | PF00069 | 0.466 |
MOD_CK2_1 | 1025 | 1031 | PF00069 | 0.475 |
MOD_CK2_1 | 1052 | 1058 | PF00069 | 0.487 |
MOD_CK2_1 | 1092 | 1098 | PF00069 | 0.524 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.466 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.509 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.509 |
MOD_CK2_1 | 965 | 971 | PF00069 | 0.524 |
MOD_GlcNHglycan | 1052 | 1055 | PF01048 | 0.331 |
MOD_GlcNHglycan | 1144 | 1147 | PF01048 | 0.324 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.272 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.381 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.516 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.266 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.418 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.571 |
MOD_GlcNHglycan | 509 | 513 | PF01048 | 0.284 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.249 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.368 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.339 |
MOD_GlcNHglycan | 868 | 872 | PF01048 | 0.385 |
MOD_GlcNHglycan | 883 | 886 | PF01048 | 0.339 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.368 |
MOD_GSK3_1 | 1048 | 1055 | PF00069 | 0.479 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.511 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.489 |
MOD_GSK3_1 | 1159 | 1166 | PF00069 | 0.509 |
MOD_GSK3_1 | 1168 | 1175 | PF00069 | 0.509 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.466 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.581 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.461 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.488 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.512 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.580 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.479 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.491 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.491 |
MOD_GSK3_1 | 893 | 900 | PF00069 | 0.422 |
MOD_N-GLC_1 | 319 | 324 | PF02516 | 0.494 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.207 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.384 |
MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.291 |
MOD_N-GLC_2 | 946 | 948 | PF02516 | 0.368 |
MOD_NEK2_1 | 1012 | 1017 | PF00069 | 0.564 |
MOD_NEK2_1 | 1052 | 1057 | PF00069 | 0.482 |
MOD_NEK2_1 | 1064 | 1069 | PF00069 | 0.466 |
MOD_NEK2_1 | 1078 | 1083 | PF00069 | 0.470 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.469 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.462 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.393 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.495 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.344 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.411 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.469 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.480 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.484 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.547 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.600 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.547 |
MOD_NEK2_1 | 959 | 964 | PF00069 | 0.585 |
MOD_NEK2_2 | 288 | 293 | PF00069 | 0.544 |
MOD_NEK2_2 | 944 | 949 | PF00069 | 0.407 |
MOD_NEK2_2 | 954 | 959 | PF00069 | 0.390 |
MOD_PIKK_1 | 1078 | 1084 | PF00454 | 0.480 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.506 |
MOD_PIKK_1 | 893 | 899 | PF00454 | 0.411 |
MOD_PIKK_1 | 960 | 966 | PF00454 | 0.425 |
MOD_PKA_2 | 1159 | 1165 | PF00069 | 0.497 |
MOD_PKA_2 | 1172 | 1178 | PF00069 | 0.509 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.425 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.528 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.461 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.486 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.466 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.466 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.523 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.466 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.488 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.568 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.477 |
MOD_Plk_1 | 71 | 77 | PF00069 | 0.568 |
MOD_Plk_1 | 795 | 801 | PF00069 | 0.489 |
MOD_Plk_4 | 1012 | 1018 | PF00069 | 0.512 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.510 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.519 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.471 |
MOD_Plk_4 | 795 | 801 | PF00069 | 0.474 |
MOD_Plk_4 | 954 | 960 | PF00069 | 0.467 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.477 |
MOD_ProDKin_1 | 1154 | 1160 | PF00069 | 0.528 |
MOD_ProDKin_1 | 1163 | 1169 | PF00069 | 0.455 |
MOD_ProDKin_1 | 929 | 935 | PF00069 | 0.524 |
MOD_SUMO_rev_2 | 451 | 456 | PF00179 | 0.479 |
TRG_DiLeu_BaEn_2 | 1136 | 1142 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 1099 | 1104 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 799 | 804 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 1148 | 1151 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 1152 | 1155 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 892 | 895 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 993 | 996 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 1101 | 1103 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.397 |
TRG_NES_CRM1_1 | 577 | 591 | PF08389 | 0.533 |
TRG_NES_CRM1_1 | 980 | 994 | PF08389 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 1041 | 1046 | PF00026 | 0.277 |
TRG_Pf-PMV_PEXEL_1 | 1101 | 1105 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 572 | 577 | PF00026 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.207 |
TRG_Pf-PMV_PEXEL_1 | 661 | 665 | PF00026 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 802 | 806 | PF00026 | 0.479 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2R6 | Leptomonas seymouri | 80% | 100% |
A0A0S4IPS1 | Bodo saltans | 48% | 99% |
A0A1X0PA85 | Trypanosomatidae | 58% | 100% |
A0A3Q8IGV8 | Leishmania donovani | 23% | 100% |
A0A3R7KSI4 | Trypanosoma rangeli | 57% | 100% |
A0A3S7X8J8 | Leishmania donovani | 89% | 100% |
A4HM28 | Leishmania braziliensis | 23% | 100% |
A4I9G2 | Leishmania infantum | 23% | 100% |
A4IAK2 | Leishmania infantum | 89% | 100% |
C9ZLN9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9B4G0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B5M6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
P41811 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P53621 | Homo sapiens | 38% | 98% |
P53622 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q0J3D9 | Oryza sativa subsp. japonica | 39% | 98% |
Q20168 | Caenorhabditis elegans | 23% | 100% |
Q27954 | Bos taurus | 38% | 98% |
Q4Q2B0 | Leishmania major | 89% | 100% |
Q4Q3L5 | Leishmania major | 23% | 100% |
Q55FR9 | Dictyostelium discoideum | 35% | 98% |
Q5VQ78 | Oryza sativa subsp. japonica | 24% | 100% |
Q6H8D5 | Oryza sativa subsp. japonica | 23% | 100% |
Q8CIE6 | Mus musculus | 38% | 98% |
Q8L828 | Arabidopsis thaliana | 24% | 100% |
Q94A40 | Arabidopsis thaliana | 39% | 98% |
Q96WV5 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 99% |
Q9AUR7 | Oryza sativa subsp. japonica | 39% | 98% |
Q9AUR8 | Oryza sativa subsp. japonica | 39% | 98% |
Q9C827 | Arabidopsis thaliana | 24% | 100% |
Q9SJT9 | Arabidopsis thaliana | 40% | 98% |
V5AUU0 | Trypanosoma cruzi | 24% | 100% |
V5DMR8 | Trypanosoma cruzi | 57% | 100% |