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:0005643 | nuclear pore | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0140513 | nuclear protein-containing complex | 2 | 10 |
GO:0031080 | nuclear pore outer ring | 3 | 4 |
GO:0016020 | membrane | 2 | 3 |
GO:0031090 | organelle membrane | 3 | 3 |
GO:0031965 | nuclear membrane | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HLR6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0008104 | protein localization | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0015031 | protein transport | 4 | 10 |
GO:0015931 | nucleobase-containing compound transport | 5 | 10 |
GO:0033036 | macromolecule localization | 2 | 10 |
GO:0045184 | establishment of protein localization | 3 | 10 |
GO:0050657 | nucleic acid transport | 6 | 10 |
GO:0050658 | RNA transport | 4 | 10 |
GO:0051028 | mRNA transport | 5 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
GO:0051236 | establishment of RNA localization | 3 | 10 |
GO:0051641 | cellular localization | 2 | 10 |
GO:0070727 | cellular macromolecule localization | 3 | 10 |
GO:0071702 | organic substance transport | 4 | 10 |
GO:0071705 | nitrogen compound transport | 4 | 10 |
GO:0000972 | transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery | 6 | 1 |
GO:0000973 | post-transcriptional tethering of RNA polymerase II gene DNA at nuclear periphery | 7 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006405 | RNA export from nucleus | 5 | 4 |
GO:0006406 | mRNA export from nucleus | 6 | 4 |
GO:0006606 | protein import into nucleus | 5 | 4 |
GO:0006886 | intracellular protein transport | 4 | 4 |
GO:0006913 | nucleocytoplasmic transport | 5 | 4 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0033365 | protein localization to organelle | 5 | 4 |
GO:0034504 | protein localization to nucleus | 6 | 4 |
GO:0046907 | intracellular transport | 3 | 4 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051168 | nuclear export | 6 | 4 |
GO:0051169 | nuclear transport | 4 | 4 |
GO:0051170 | import into nucleus | 6 | 4 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 4 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 4 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 10 |
GO:0017056 | structural constituent of nuclear pore | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.448 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 757 | 759 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.355 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.350 |
DEG_APCC_DBOX_1 | 543 | 551 | PF00400 | 0.480 |
DEG_APCC_DBOX_1 | 666 | 674 | PF00400 | 0.479 |
DEG_APCC_DBOX_1 | 704 | 712 | PF00400 | 0.470 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.603 |
DOC_CYCLIN_RxL_1 | 78 | 86 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 544 | 550 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 224 | 231 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 390 | 397 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 408 | 417 | PF00069 | 0.298 |
DOC_MAPK_RevD_3 | 530 | 545 | PF00069 | 0.493 |
DOC_PIKK_1 | 149 | 156 | PF02985 | 0.393 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.238 |
DOC_PP1_RVXF_1 | 493 | 499 | PF00149 | 0.476 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 733 | 737 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.663 |
DOC_USP7_MATH_2 | 345 | 351 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.470 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.638 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 354 | 362 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 408 | 417 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 514 | 524 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 568 | 577 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 600 | 609 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 667 | 677 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 678 | 686 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 748 | 752 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.407 |
LIG_Actin_WH2_2 | 35 | 51 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 76 | 91 | PF00022 | 0.391 |
LIG_APCC_ABBA_1 | 131 | 136 | PF00400 | 0.337 |
LIG_BIR_III_4 | 17 | 21 | PF00653 | 0.552 |
LIG_deltaCOP1_diTrp_1 | 270 | 276 | PF00928 | 0.529 |
LIG_eIF4E_1 | 222 | 228 | PF01652 | 0.437 |
LIG_eIF4E_1 | 726 | 732 | PF01652 | 0.416 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.424 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.375 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.337 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.479 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.515 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.475 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.434 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.443 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.359 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.336 |
LIG_FHA_1 | 773 | 779 | PF00498 | 0.457 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.426 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.446 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.533 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.544 |
LIG_FHA_2 | 581 | 587 | PF00498 | 0.473 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.433 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.471 |
LIG_FHA_2 | 769 | 775 | PF00498 | 0.427 |
LIG_GBD_Chelix_1 | 280 | 288 | PF00786 | 0.391 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 217 | 228 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 33 | 42 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 338 | 345 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 425 | 434 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 507 | 517 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 738 | 749 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 507 | 512 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 738 | 744 | PF02991 | 0.394 |
LIG_MYND_1 | 729 | 733 | PF01753 | 0.418 |
LIG_NRBOX | 644 | 650 | PF00104 | 0.281 |
LIG_PCNA_yPIPBox_3 | 480 | 491 | PF02747 | 0.310 |
LIG_Pex14_1 | 272 | 276 | PF04695 | 0.455 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.639 |
LIG_SH2_SRC | 137 | 140 | PF00017 | 0.547 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.389 |
LIG_SH2_SRC | 5 | 8 | PF00017 | 0.523 |
LIG_SH2_SRC | 726 | 729 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 103 | 107 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 427 | 431 | PF00017 | 0.343 |
LIG_SH2_STAT3 | 437 | 440 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.420 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.470 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.589 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.432 |
LIG_SH3_3 | 727 | 733 | PF00018 | 0.318 |
LIG_Sin3_3 | 190 | 197 | PF02671 | 0.465 |
LIG_SUMO_SIM_anti_2 | 357 | 364 | PF11976 | 0.368 |
LIG_SUMO_SIM_anti_2 | 507 | 514 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 357 | 364 | PF11976 | 0.368 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.457 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.453 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.381 |
MOD_CDK_SPxxK_3 | 698 | 705 | PF00069 | 0.564 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.622 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.635 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.344 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.371 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.489 |
MOD_CK1_1 | 573 | 579 | PF00069 | 0.705 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.534 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.420 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.525 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.509 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.398 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.433 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.430 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.488 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.575 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.517 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.516 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.479 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.420 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.356 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.647 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.619 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.694 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.529 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.526 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.735 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.427 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.436 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.464 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.442 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.607 |
MOD_GlcNHglycan | 735 | 738 | PF01048 | 0.371 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.517 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.351 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.327 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.622 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.469 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.496 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.529 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.456 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.439 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.663 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.557 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.479 |
MOD_GSK3_1 | 678 | 685 | PF00069 | 0.416 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.461 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.524 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.379 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.533 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.535 |
MOD_N-GLC_1 | 629 | 634 | PF02516 | 0.559 |
MOD_N-GLC_1 | 768 | 773 | PF02516 | 0.401 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.581 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.431 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.700 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.385 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.393 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.280 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.506 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.440 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.511 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.587 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.367 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.456 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.540 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.508 |
MOD_PIKK_1 | 649 | 655 | PF00454 | 0.391 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.371 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.493 |
MOD_PKA_2 | 747 | 753 | PF00069 | 0.495 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.378 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.433 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.502 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.371 |
MOD_Plk_1 | 536 | 542 | PF00069 | 0.403 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.421 |
MOD_Plk_1 | 588 | 594 | PF00069 | 0.466 |
MOD_Plk_1 | 629 | 635 | PF00069 | 0.449 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.501 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.433 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.616 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.369 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.418 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.369 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.304 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.480 |
MOD_Plk_4 | 672 | 678 | PF00069 | 0.329 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.403 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.442 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.605 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.538 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.673 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.635 |
MOD_SUMO_rev_2 | 342 | 350 | PF00179 | 0.328 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.381 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.379 |
TRG_DiLeu_BaEn_4 | 75 | 81 | PF01217 | 0.466 |
TRG_DiLeu_LyEn_5 | 351 | 356 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 415 | 418 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 48 | 50 | PF00400 | 0.190 |
TRG_ER_diArg_1 | 513 | 515 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 764 | 767 | PF00400 | 0.585 |
TRG_NES_CRM1_1 | 405 | 419 | PF08389 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 545 | 549 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 631 | 636 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 678 | 682 | PF00026 | 0.355 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAQ9 | Leptomonas seymouri | 75% | 88% |
A0A0S4J8I7 | Bodo saltans | 31% | 100% |
A0A1X0P3M8 | Trypanosomatidae | 44% | 100% |
A0A3Q8IMG5 | Leishmania donovani | 89% | 100% |
A0A422N462 | Trypanosoma rangeli | 44% | 99% |
A4I942 | Leishmania infantum | 89% | 100% |
D0A6A9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
E9B442 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q3Y3 | Leishmania major | 89% | 100% |