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: 3 |
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: 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:0005814 | centriole | 5 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0005929 | cilium | 4 | 12 |
GO:0030990 | intraciliary transport particle | 2 | 2 |
GO:0031514 | motile cilium | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0097546 | ciliary base | 2 | 2 |
GO:0097730 | non-motile cilium | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AD91
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007018 | microtubule-based movement | 3 | 2 |
GO:0007163 | establishment or maintenance of cell polarity | 2 | 2 |
GO:0008361 | regulation of cell size | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010970 | transport along microtubule | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030010 | establishment of cell polarity | 3 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0031503 | protein-containing complex localization | 2 | 2 |
GO:0032535 | regulation of cellular component size | 4 | 2 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 2 |
GO:0042073 | intraciliary transport | 3 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090066 | regulation of anatomical structure size | 3 | 2 |
GO:0099111 | microtubule-based transport | 4 | 2 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
GO:1905515 | non-motile cilium assembly | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
GO:0019894 | kinesin binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 780 | 784 | PF00656 | 0.708 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 673 | 675 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 745 | 747 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 760 | 762 | PF00675 | 0.524 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 656 | 658 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 665 | 667 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.752 |
CLV_PCSK_KEX2_1 | 760 | 762 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 792 | 794 | PF00082 | 0.755 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 318 | 320 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 535 | 537 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 665 | 667 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 792 | 794 | PF00082 | 0.755 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 795 | 799 | PF00082 | 0.738 |
DEG_Kelch_Keap1_1 | 458 | 463 | PF01344 | 0.360 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.729 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.681 |
DOC_CDC14_PxL_1 | 113 | 121 | PF14671 | 0.591 |
DOC_CKS1_1 | 12 | 17 | PF01111 | 0.673 |
DOC_CYCLIN_RxL_1 | 519 | 529 | PF00134 | 0.287 |
DOC_CYCLIN_yCln2_LP_2 | 374 | 380 | PF00134 | 0.453 |
DOC_MAPK_gen_1 | 343 | 349 | PF00069 | 0.607 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 627 | 634 | PF00149 | 0.360 |
DOC_PP1_RVXF_1 | 82 | 89 | PF00149 | 0.605 |
DOC_PP2B_LxvP_1 | 374 | 377 | PF13499 | 0.320 |
DOC_PP4_FxxP_1 | 12 | 15 | PF00568 | 0.663 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.738 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 797 | 801 | PF00917 | 0.668 |
DOC_USP7_UBL2_3 | 136 | 140 | PF12436 | 0.415 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.379 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.434 |
DOC_USP7_UBL2_3 | 432 | 436 | PF12436 | 0.402 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.407 |
DOC_USP7_UBL2_3 | 703 | 707 | PF12436 | 0.432 |
DOC_USP7_UBL2_3 | 792 | 796 | PF12436 | 0.778 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.321 |
LIG_14-3-3_CanoR_1 | 636 | 642 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 744 | 753 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 78 | 86 | PF00244 | 0.606 |
LIG_APCC_ABBA_1 | 524 | 529 | PF00400 | 0.287 |
LIG_APCC_ABBA_1 | 774 | 779 | PF00400 | 0.447 |
LIG_APCC_ABBAyCdc20_2 | 523 | 529 | PF00400 | 0.302 |
LIG_EH_1 | 26 | 30 | PF12763 | 0.732 |
LIG_eIF4E_1 | 465 | 471 | PF01652 | 0.437 |
LIG_eIF4E_1 | 475 | 481 | PF01652 | 0.341 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.704 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.346 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.360 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.394 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.526 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.477 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.372 |
LIG_GBD_Chelix_1 | 180 | 188 | PF00786 | 0.431 |
LIG_Integrin_RGD_1 | 658 | 660 | PF01839 | 0.344 |
LIG_LIR_Apic_2 | 26 | 32 | PF02991 | 0.762 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 212 | 220 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 287 | 292 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 301 | 310 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 320 | 329 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 463 | 472 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 564 | 574 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 6 | 17 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 644 | 652 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 320 | 324 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 602 | 607 | PF02991 | 0.360 |
LIG_PALB2_WD40_1 | 561 | 569 | PF16756 | 0.343 |
LIG_PCNA_yPIPBox_3 | 605 | 617 | PF02747 | 0.340 |
LIG_Pex14_1 | 383 | 387 | PF04695 | 0.330 |
LIG_Pex14_1 | 616 | 620 | PF04695 | 0.313 |
LIG_PTB_Apo_2 | 216 | 223 | PF02174 | 0.398 |
LIG_PTB_Apo_2 | 621 | 628 | PF02174 | 0.349 |
LIG_PTB_Phospho_1 | 621 | 627 | PF10480 | 0.345 |
LIG_REV1ctd_RIR_1 | 631 | 640 | PF16727 | 0.356 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.353 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.434 |
LIG_SH2_CRK | 387 | 391 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 200 | 203 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 459 | 462 | PF00017 | 0.470 |
LIG_SH2_SRC | 200 | 203 | PF00017 | 0.375 |
LIG_SH2_SRC | 387 | 390 | PF00017 | 0.453 |
LIG_SH2_SRC | 424 | 427 | PF00017 | 0.493 |
LIG_SH2_SRC | 459 | 462 | PF00017 | 0.470 |
LIG_SH2_SRC | 527 | 530 | PF00017 | 0.287 |
LIG_SH2_SRC | 548 | 551 | PF00017 | 0.322 |
LIG_SH2_SRC | 600 | 603 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.321 |
LIG_SH2_STAT3 | 684 | 687 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.156 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 661 | 664 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.339 |
LIG_SH3_2 | 115 | 120 | PF14604 | 0.592 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.582 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.529 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.380 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.316 |
LIG_SUMO_SIM_anti_2 | 466 | 472 | PF11976 | 0.441 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.507 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.781 |
LIG_TYR_ITIM | 306 | 311 | PF00017 | 0.321 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.420 |
LIG_UBA3_1 | 147 | 152 | PF00899 | 0.452 |
LIG_UBA3_1 | 243 | 251 | PF00899 | 0.287 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.645 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.407 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.378 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.613 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.701 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.579 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.523 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.354 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.363 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.637 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.729 |
MOD_CK2_1 | 799 | 805 | PF00069 | 0.692 |
MOD_Cter_Amidation | 758 | 761 | PF01082 | 0.652 |
MOD_GlcNHglycan | 143 | 147 | PF01048 | 0.370 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.620 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.687 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.679 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.688 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.642 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.412 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.347 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.592 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.600 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.547 |
MOD_LATS_1 | 742 | 748 | PF00433 | 0.757 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.434 |
MOD_N-GLC_1 | 484 | 489 | PF02516 | 0.474 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.494 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.381 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.287 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.486 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.672 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.490 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.726 |
MOD_PK_1 | 770 | 776 | PF00069 | 0.624 |
MOD_PKA_1 | 120 | 126 | PF00069 | 0.685 |
MOD_PKA_1 | 744 | 750 | PF00069 | 0.769 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.284 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.382 |
MOD_PKA_2 | 744 | 750 | PF00069 | 0.731 |
MOD_PKB_1 | 442 | 450 | PF00069 | 0.328 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.376 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.533 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.274 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.434 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.502 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.554 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.365 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.483 |
MOD_Plk_1 | 729 | 735 | PF00069 | 0.722 |
MOD_Plk_1 | 770 | 776 | PF00069 | 0.679 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.372 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.441 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.384 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.632 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.321 |
MOD_SUMO_for_1 | 622 | 625 | PF00179 | 0.358 |
MOD_SUMO_rev_2 | 778 | 786 | PF00179 | 0.718 |
TRG_DiLeu_BaEn_4 | 143 | 149 | PF01217 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.324 |
TRG_DiLeu_BaLyEn_6 | 565 | 570 | PF01217 | 0.377 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.103 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.544 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 360 | 363 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 441 | 444 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 656 | 658 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 673 | 675 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 744 | 746 | PF00400 | 0.773 |
TRG_NES_CRM1_1 | 187 | 201 | PF08389 | 0.341 |
TRG_NES_CRM1_1 | 677 | 691 | PF08389 | 0.349 |
TRG_NLS_MonoExtC_3 | 791 | 796 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 792 | 799 | PF00514 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 665 | 669 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBZ3 | Leptomonas seymouri | 81% | 99% |
A0A0S4JJR3 | Bodo saltans | 67% | 100% |
A0A1X0P453 | Trypanosomatidae | 66% | 100% |
A0A3Q8IDD3 | Leishmania donovani | 98% | 100% |
A0A3R7M723 | Trypanosoma rangeli | 65% | 100% |
A4HFN8 | Leishmania braziliensis | 92% | 100% |
A4I2R4 | Leishmania infantum | 98% | 100% |
D0A5X0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
E9AZ16 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q13099 | Homo sapiens | 43% | 98% |
Q61371 | Mus musculus | 42% | 98% |
V5B8M5 | Trypanosoma cruzi | 67% | 93% |