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. | no | yes: 0 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005635 | nuclear envelope | 4 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0031967 | organelle envelope | 3 | 2 |
GO:0031975 | envelope | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q9E4
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 2 |
GO:0006810 | transport | 3 | 4 |
GO:0006886 | intracellular protein transport | 4 | 4 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0008104 | protein localization | 4 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0015031 | protein transport | 4 | 4 |
GO:0033036 | macromolecule localization | 2 | 4 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0034504 | protein localization to nucleus | 6 | 2 |
GO:0045184 | establishment of protein localization | 3 | 4 |
GO:0046907 | intracellular transport | 3 | 4 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051170 | import into nucleus | 6 | 2 |
GO:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
GO:0051641 | cellular localization | 2 | 4 |
GO:0051649 | establishment of localization in cell | 3 | 4 |
GO:0070727 | cellular macromolecule localization | 3 | 4 |
GO:0071702 | organic substance transport | 4 | 4 |
GO:0071705 | nitrogen compound transport | 4 | 4 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0019899 | enzyme binding | 3 | 2 |
GO:0031267 | small GTPase binding | 5 | 2 |
GO:0051020 | GTPase binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.510 |
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.593 |
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.530 |
CLV_Separin_Metazoa | 18 | 22 | PF03568 | 0.475 |
DEG_APCC_DBOX_1 | 127 | 135 | PF00400 | 0.557 |
DEG_APCC_DBOX_1 | 486 | 494 | PF00400 | 0.499 |
DEG_APCC_DBOX_1 | 527 | 535 | PF00400 | 0.454 |
DEG_APCC_DBOX_1 | 64 | 72 | PF00400 | 0.477 |
DEG_SCF_FBW7_1 | 313 | 319 | PF00400 | 0.461 |
DEG_SPOP_SBC_1 | 387 | 391 | PF00917 | 0.587 |
DOC_CKS1_1 | 313 | 318 | PF01111 | 0.643 |
DOC_CYCLIN_RxL_1 | 259 | 268 | PF00134 | 0.449 |
DOC_CYCLIN_RxL_1 | 339 | 350 | PF00134 | 0.416 |
DOC_CYCLIN_RxL_1 | 486 | 495 | PF00134 | 0.445 |
DOC_CYCLIN_RxL_1 | 95 | 103 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 288 | 294 | PF00134 | 0.403 |
DOC_CYCLIN_yCln2_LP_2 | 493 | 499 | PF00134 | 0.470 |
DOC_MAPK_gen_1 | 112 | 120 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 160 | 168 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 284 | 292 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 546 | 554 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 747 | 756 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 879 | 888 | PF00069 | 0.325 |
DOC_MAPK_MEF2A_6 | 951 | 960 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 341 | 348 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 506 | 513 | PF00149 | 0.316 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.418 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.526 |
DOC_PP4_FxxP_1 | 623 | 626 | PF00568 | 0.493 |
DOC_PP4_FxxP_1 | 729 | 732 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 867 | 871 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 873 | 877 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 931 | 935 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 936 | 940 | PF00917 | 0.750 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.282 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 888 | 893 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 160 | 164 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 367 | 373 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 528 | 538 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 757 | 763 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 807 | 813 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 909 | 914 | PF00244 | 0.581 |
LIG_Actin_WH2_2 | 665 | 683 | PF00022 | 0.544 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 725 | 729 | PF00533 | 0.507 |
LIG_CtBP_PxDLS_1 | 61 | 65 | PF00389 | 0.310 |
LIG_deltaCOP1_diTrp_1 | 712 | 719 | PF00928 | 0.477 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.415 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.382 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.537 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.384 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.473 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.210 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.404 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.468 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.501 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.507 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.453 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.453 |
LIG_FHA_1 | 835 | 841 | PF00498 | 0.463 |
LIG_FHA_1 | 910 | 916 | PF00498 | 0.507 |
LIG_FHA_1 | 935 | 941 | PF00498 | 0.738 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.545 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.554 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.524 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.407 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.528 |
LIG_FHA_2 | 850 | 856 | PF00498 | 0.531 |
LIG_FHA_2 | 939 | 945 | PF00498 | 0.728 |
LIG_GBD_Chelix_1 | 405 | 413 | PF00786 | 0.628 |
LIG_LIR_Apic_2 | 370 | 376 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 726 | 732 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 14 | 24 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 162 | 171 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 424 | 435 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 479 | 490 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 713 | 722 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 874 | 885 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 479 | 485 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 713 | 719 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 746 | 752 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 874 | 880 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.408 |
LIG_MLH1_MIPbox_1 | 370 | 374 | PF16413 | 0.548 |
LIG_NRBOX | 489 | 495 | PF00104 | 0.301 |
LIG_NRBOX | 668 | 674 | PF00104 | 0.433 |
LIG_NRBOX | 899 | 905 | PF00104 | 0.420 |
LIG_NRBOX | 956 | 962 | PF00104 | 0.571 |
LIG_PCNA_PIPBox_1 | 379 | 388 | PF02747 | 0.499 |
LIG_PCNA_yPIPBox_3 | 139 | 151 | PF02747 | 0.538 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.385 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.469 |
LIG_SH2_CRK | 760 | 764 | PF00017 | 0.352 |
LIG_SH2_CRK | 877 | 881 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.495 |
LIG_SH2_PTP2 | 163 | 166 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 96 | 99 | PF00017 | 0.488 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 634 | 638 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 760 | 764 | PF00017 | 0.395 |
LIG_SH2_STAP1 | 877 | 881 | PF00017 | 0.536 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 760 | 763 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.396 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.447 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.610 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.505 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.560 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.346 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.543 |
LIG_SH3_3 | 693 | 699 | PF00018 | 0.407 |
LIG_SH3_3 | 770 | 776 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 761 | 766 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 882 | 889 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 550 | 558 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 842 | 847 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 882 | 889 | PF11976 | 0.391 |
LIG_TRAF2_1 | 582 | 585 | PF00917 | 0.561 |
LIG_TYR_ITIM | 161 | 166 | PF00017 | 0.475 |
LIG_TYR_ITIM | 758 | 763 | PF00017 | 0.458 |
LIG_UBA3_1 | 165 | 173 | PF00899 | 0.355 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.459 |
MOD_CDK_SPxxK_3 | 254 | 261 | PF00069 | 0.402 |
MOD_CDK_SPxxK_3 | 327 | 334 | PF00069 | 0.311 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.484 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.458 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.771 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.459 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.608 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.457 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.609 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.356 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.479 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.557 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.530 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.529 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.493 |
MOD_CK1_1 | 847 | 853 | PF00069 | 0.548 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.553 |
MOD_CK1_1 | 934 | 940 | PF00069 | 0.662 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.518 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.541 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.430 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.562 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.461 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.474 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.534 |
MOD_CK2_1 | 849 | 855 | PF00069 | 0.558 |
MOD_DYRK1A_RPxSP_1 | 589 | 593 | PF00069 | 0.590 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.401 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.747 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.766 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.463 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.464 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.512 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.533 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.588 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.532 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.592 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.548 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.448 |
MOD_GlcNHglycan | 808 | 811 | PF01048 | 0.332 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.377 |
MOD_GlcNHglycan | 849 | 852 | PF01048 | 0.536 |
MOD_GlcNHglycan | 873 | 876 | PF01048 | 0.641 |
MOD_GlcNHglycan | 933 | 936 | PF01048 | 0.569 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.501 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.463 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.386 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.686 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.414 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.722 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.604 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.308 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.432 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.533 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.436 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.582 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.470 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.421 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.368 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.503 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.361 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.437 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.471 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.519 |
MOD_GSK3_1 | 867 | 874 | PF00069 | 0.606 |
MOD_GSK3_1 | 890 | 897 | PF00069 | 0.467 |
MOD_GSK3_1 | 930 | 937 | PF00069 | 0.637 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.689 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.464 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.405 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.450 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.532 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.382 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.524 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.467 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.383 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.441 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.371 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.463 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.376 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.483 |
MOD_NEK2_1 | 844 | 849 | PF00069 | 0.458 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.511 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.325 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.491 |
MOD_NEK2_2 | 368 | 373 | PF00069 | 0.458 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.502 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.546 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.565 |
MOD_PIKK_1 | 720 | 726 | PF00454 | 0.259 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.499 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.515 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.528 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.564 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.410 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.514 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.397 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.455 |
MOD_PKA_2 | 786 | 792 | PF00069 | 0.574 |
MOD_PKA_2 | 806 | 812 | PF00069 | 0.239 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.500 |
MOD_PKA_2 | 908 | 914 | PF00069 | 0.596 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.469 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.483 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.480 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.555 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.400 |
MOD_Plk_2-3 | 478 | 484 | PF00069 | 0.333 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.439 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.457 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.419 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.452 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.466 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.448 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.479 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.369 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.492 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.395 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.377 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.391 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.494 |
MOD_Plk_4 | 891 | 897 | PF00069 | 0.509 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.515 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.629 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.769 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.630 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.296 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.538 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.440 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.450 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.479 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.557 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.562 |
MOD_ProDKin_1 | 888 | 894 | PF00069 | 0.418 |
TRG_DiLeu_BaEn_1 | 882 | 887 | PF01217 | 0.380 |
TRG_DiLeu_BaEn_2 | 62 | 68 | PF01217 | 0.326 |
TRG_DiLeu_BaEn_4 | 855 | 861 | PF01217 | 0.606 |
TRG_DiLeu_BaLyEn_6 | 262 | 267 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 319 | 324 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 373 | 378 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 899 | 904 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 760 | 763 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 877 | 880 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.343 |
TRG_NES_CRM1_1 | 63 | 77 | PF08389 | 0.484 |
TRG_NLS_MonoExtC_3 | 260 | 265 | PF00514 | 0.347 |
TRG_NLS_MonoExtN_4 | 258 | 265 | PF00514 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 37 | 41 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 98 | 103 | PF00026 | 0.538 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4A0 | Leptomonas seymouri | 60% | 99% |
A0A1X0NSG1 | Trypanosomatidae | 36% | 99% |
A0A3Q8INY0 | Leishmania donovani | 93% | 100% |
A0A3S5IS01 | Trypanosoma rangeli | 37% | 100% |
A4HEQ3 | Leishmania braziliensis | 81% | 100% |
A4I1Y2 | Leishmania infantum | 93% | 100% |
C9ZS36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AY29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 96% |
V5BUJ9 | Trypanosoma cruzi | 33% | 100% |