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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QE53
Term | Name | Level | Count |
---|---|---|---|
GO:0000054 | ribosomal subunit export from nucleus | 3 | 9 |
GO:0000055 | ribosomal large subunit export from nucleus | 4 | 9 |
GO:0006810 | transport | 3 | 9 |
GO:0006913 | nucleocytoplasmic transport | 5 | 9 |
GO:0006996 | organelle organization | 4 | 9 |
GO:0007010 | cytoskeleton organization | 5 | 9 |
GO:0008104 | protein localization | 4 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0015031 | protein transport | 4 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 9 |
GO:0030029 | actin filament-based process | 2 | 9 |
GO:0030036 | actin cytoskeleton organization | 3 | 9 |
GO:0031503 | protein-containing complex localization | 2 | 9 |
GO:0033036 | macromolecule localization | 2 | 9 |
GO:0033750 | ribosome localization | 3 | 9 |
GO:0042273 | ribosomal large subunit biogenesis | 5 | 9 |
GO:0044085 | cellular component biogenesis | 3 | 9 |
GO:0045184 | establishment of protein localization | 3 | 9 |
GO:0046907 | intracellular transport | 3 | 9 |
GO:0051168 | nuclear export | 6 | 9 |
GO:0051169 | nuclear transport | 4 | 9 |
GO:0051179 | localization | 1 | 9 |
GO:0051234 | establishment of localization | 2 | 9 |
GO:0051640 | organelle localization | 2 | 9 |
GO:0051641 | cellular localization | 2 | 9 |
GO:0051649 | establishment of localization in cell | 3 | 9 |
GO:0051656 | establishment of organelle localization | 3 | 9 |
GO:0070727 | cellular macromolecule localization | 3 | 9 |
GO:0071702 | organic substance transport | 4 | 9 |
GO:0071705 | nitrogen compound transport | 4 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.448 |
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.369 |
CLV_C14_Caspase3-7 | 523 | 527 | PF00656 | 0.306 |
CLV_C14_Caspase3-7 | 532 | 536 | PF00656 | 0.260 |
CLV_C14_Caspase3-7 | 540 | 544 | PF00656 | 0.223 |
CLV_C14_Caspase3-7 | 571 | 575 | PF00656 | 0.451 |
CLV_C14_Caspase3-7 | 605 | 609 | PF00656 | 0.360 |
CLV_C14_Caspase3-7 | 612 | 616 | PF00656 | 0.361 |
CLV_C14_Caspase3-7 | 683 | 687 | PF00656 | 0.329 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 792 | 794 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.302 |
CLV_PCSK_FUR_1 | 16 | 20 | PF00082 | 0.441 |
CLV_PCSK_FUR_1 | 741 | 745 | PF00082 | 0.459 |
CLV_PCSK_FUR_1 | 858 | 862 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.132 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 743 | 745 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 827 | 829 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 860 | 862 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 743 | 745 | PF00082 | 0.375 |
CLV_PCSK_PC1ET2_1 | 753 | 755 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 777 | 779 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 818 | 820 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 827 | 829 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 860 | 862 | PF00082 | 0.408 |
CLV_PCSK_PC7_1 | 408 | 414 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.320 |
CLV_Separin_Metazoa | 79 | 83 | PF03568 | 0.462 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.403 |
DEG_APCC_DBOX_1 | 6 | 14 | PF00400 | 0.430 |
DEG_APCC_DBOX_1 | 818 | 826 | PF00400 | 0.327 |
DEG_Kelch_Keap1_1 | 515 | 520 | PF01344 | 0.392 |
DEG_SPOP_SBC_1 | 514 | 518 | PF00917 | 0.385 |
DEG_SPOP_SBC_1 | 707 | 711 | PF00917 | 0.423 |
DOC_ANK_TNKS_1 | 571 | 578 | PF00023 | 0.385 |
DOC_CDC14_PxL_1 | 483 | 491 | PF14671 | 0.322 |
DOC_CYCLIN_RxL_1 | 126 | 136 | PF00134 | 0.468 |
DOC_MAPK_DCC_7 | 290 | 298 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 126 | 135 | PF00069 | 0.401 |
DOC_MAPK_HePTP_8 | 174 | 186 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 177 | 186 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 851 | 858 | PF00149 | 0.327 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.444 |
DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.549 |
DOC_PP4_MxPP_1 | 373 | 376 | PF00568 | 0.394 |
DOC_SPAK_OSR1_1 | 319 | 323 | PF12202 | 0.412 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.320 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.481 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.488 |
DOC_USP7_UBL2_3 | 255 | 259 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 794 | 798 | PF12436 | 0.345 |
DOC_USP7_UBL2_3 | 804 | 808 | PF12436 | 0.309 |
DOC_USP7_UBL2_3 | 848 | 852 | PF12436 | 0.328 |
DOC_USP7_UBL2_3 | 856 | 860 | PF12436 | 0.329 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.268 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 315 | 322 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 36 | 43 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 717 | 724 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 793 | 801 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 69 | 84 | PF00022 | 0.408 |
LIG_APCC_ABBA_1 | 116 | 121 | PF00400 | 0.398 |
LIG_APCC_ABBA_1 | 446 | 451 | PF00400 | 0.360 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.550 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.550 |
LIG_BIR_III_4 | 574 | 578 | PF00653 | 0.385 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 795 | 799 | PF00533 | 0.408 |
LIG_CtBP_PxDLS_1 | 664 | 668 | PF00389 | 0.229 |
LIG_CtBP_PxDLS_1 | 90 | 94 | PF00389 | 0.346 |
LIG_FAT_LD_1 | 306 | 314 | PF03623 | 0.396 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.477 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.465 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.374 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.384 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.410 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.385 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.357 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.438 |
LIG_FHA_1 | 708 | 714 | PF00498 | 0.346 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.432 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.546 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.394 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.381 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.458 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.455 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.430 |
LIG_FHA_2 | 718 | 724 | PF00498 | 0.360 |
LIG_FHA_2 | 810 | 816 | PF00498 | 0.327 |
LIG_GBD_Chelix_1 | 305 | 313 | PF00786 | 0.301 |
LIG_Integrin_RGD_1 | 433 | 435 | PF01839 | 0.327 |
LIG_LIR_Apic_2 | 349 | 354 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 490 | 500 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 535 | 546 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 637 | 647 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 679 | 688 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 721 | 730 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 679 | 684 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 721 | 727 | PF02991 | 0.327 |
LIG_LRP6_Inhibitor_1 | 402 | 408 | PF00058 | 0.382 |
LIG_LYPXL_S_1 | 452 | 456 | PF13949 | 0.327 |
LIG_LYPXL_yS_3 | 453 | 456 | PF13949 | 0.327 |
LIG_MYND_1 | 454 | 458 | PF01753 | 0.327 |
LIG_MYND_1 | 557 | 561 | PF01753 | 0.408 |
LIG_PALB2_WD40_1 | 676 | 684 | PF16756 | 0.462 |
LIG_PCNA_yPIPBox_3 | 297 | 310 | PF02747 | 0.317 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.379 |
LIG_PTB_Apo_2 | 46 | 53 | PF02174 | 0.422 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 483 | 487 | PF00017 | 0.322 |
LIG_SH2_SRC | 326 | 329 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.346 |
LIG_SUMO_SIM_anti_2 | 100 | 105 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 197 | 202 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 180 | 185 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 193 | 202 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 360 | 366 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 590 | 596 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 661 | 668 | PF11976 | 0.325 |
LIG_TRAF2_1 | 545 | 548 | PF00917 | 0.462 |
LIG_TRAF2_1 | 656 | 659 | PF00917 | 0.344 |
LIG_TYR_ITIM | 324 | 329 | PF00017 | 0.405 |
LIG_TYR_ITIM | 491 | 496 | PF00017 | 0.423 |
LIG_UBA3_1 | 101 | 107 | PF00899 | 0.403 |
LIG_UBA3_1 | 422 | 430 | PF00899 | 0.327 |
LIG_UBA3_1 | 822 | 827 | PF00899 | 0.327 |
MOD_CDK_SPK_2 | 693 | 698 | PF00069 | 0.268 |
MOD_CDK_SPxxK_3 | 207 | 214 | PF00069 | 0.537 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.402 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.500 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.470 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.357 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.373 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.284 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.387 |
MOD_CK1_1 | 708 | 714 | PF00069 | 0.438 |
MOD_CK1_1 | 736 | 742 | PF00069 | 0.360 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.579 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.375 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.381 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.426 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.299 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.396 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.175 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.392 |
MOD_CK2_1 | 641 | 647 | PF00069 | 0.379 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.352 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.327 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.327 |
MOD_Cter_Amidation | 741 | 744 | PF01082 | 0.385 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.461 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.497 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.556 |
MOD_GlcNHglycan | 502 | 507 | PF01048 | 0.380 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.319 |
MOD_GlcNHglycan | 543 | 547 | PF01048 | 0.456 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.371 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.283 |
MOD_GlcNHglycan | 604 | 608 | PF01048 | 0.428 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.359 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.437 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.419 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.387 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.439 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.423 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.339 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.444 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.362 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.317 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.355 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.332 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.346 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.327 |
MOD_LATS_1 | 34 | 40 | PF00433 | 0.405 |
MOD_N-GLC_1 | 14 | 19 | PF02516 | 0.436 |
MOD_N-GLC_1 | 691 | 696 | PF02516 | 0.362 |
MOD_N-GLC_1 | 809 | 814 | PF02516 | 0.327 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.419 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.428 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.599 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.408 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.423 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.385 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.383 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.359 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.422 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.462 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.229 |
MOD_NEK2_1 | 809 | 814 | PF00069 | 0.355 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.359 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.327 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.285 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.296 |
MOD_NEK2_2 | 403 | 408 | PF00069 | 0.379 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.429 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.511 |
MOD_PIKK_1 | 593 | 599 | PF00454 | 0.411 |
MOD_PIKK_1 | 729 | 735 | PF00454 | 0.385 |
MOD_PIKK_1 | 826 | 832 | PF00454 | 0.324 |
MOD_PK_1 | 226 | 232 | PF00069 | 0.624 |
MOD_PK_1 | 698 | 704 | PF00069 | 0.401 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.499 |
MOD_PKA_1 | 777 | 783 | PF00069 | 0.346 |
MOD_PKA_1 | 793 | 799 | PF00069 | 0.358 |
MOD_PKA_1 | 804 | 810 | PF00069 | 0.275 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.568 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.371 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.463 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.568 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.345 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.438 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.376 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.401 |
MOD_PKA_2 | 842 | 848 | PF00069 | 0.408 |
MOD_PKB_1 | 188 | 196 | PF00069 | 0.492 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.400 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.410 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.404 |
MOD_Plk_2-3 | 194 | 200 | PF00069 | 0.437 |
MOD_Plk_2-3 | 20 | 26 | PF00069 | 0.535 |
MOD_Plk_2-3 | 520 | 526 | PF00069 | 0.408 |
MOD_Plk_2-3 | 549 | 555 | PF00069 | 0.417 |
MOD_Plk_2-3 | 641 | 647 | PF00069 | 0.417 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.459 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.438 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.408 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.552 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.268 |
MOD_SUMO_for_1 | 784 | 787 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 849 | 857 | PF00179 | 0.327 |
TRG_DiLeu_BaLyEn_6 | 294 | 299 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 714 | 719 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.186 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.295 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 801 | 803 | PF00400 | 0.359 |
TRG_NLS_Bipartite_1 | 793 | 809 | PF00514 | 0.341 |
TRG_NLS_MonoCore_2 | 802 | 807 | PF00514 | 0.319 |
TRG_NLS_MonoExtC_3 | 581 | 587 | PF00514 | 0.359 |
TRG_NLS_MonoExtC_3 | 803 | 808 | PF00514 | 0.322 |
TRG_NLS_MonoExtN_4 | 580 | 586 | PF00514 | 0.411 |
TRG_NLS_MonoExtN_4 | 802 | 809 | PF00514 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 443 | 447 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 717 | 721 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7R9 | Leptomonas seymouri | 73% | 100% |
A0A1X0NT40 | Trypanosomatidae | 70% | 100% |
A0A3S5H720 | Leishmania donovani | 94% | 99% |
A4H993 | Leishmania braziliensis | 84% | 100% |
A4HXL4 | Leishmania infantum | 94% | 99% |
C9ZPA8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9ARB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P53313 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |