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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 9 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:1990904 | ribonucleoprotein complex | 2 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005868 | cytoplasmic dynein complex | 4 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0030286 | dynein complex | 3 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A4HF77
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 4 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0042073 | intraciliary transport | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0099111 | microtubule-based transport | 4 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 3 |
GO:0005515 | protein binding | 2 | 1 |
GO:0045503 | dynein light chain binding | 3 | 1 |
GO:0045504 | dynein heavy chain binding | 3 | 1 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0030515 | snoRNA binding | 5 | 2 |
GO:0034511 | U3 snoRNA binding | 6 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004672 | protein kinase activity | 3 | 1 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.320 |
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.683 |
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 599 | 603 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.475 |
CLV_PCSK_FUR_1 | 222 | 226 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 649 | 651 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 649 | 651 | PF00082 | 0.549 |
CLV_PCSK_PC7_1 | 538 | 544 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.557 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.291 |
DEG_SPOP_SBC_1 | 108 | 112 | PF00917 | 0.525 |
DOC_MAPK_gen_1 | 311 | 318 | PF00069 | 0.737 |
DOC_MAPK_gen_1 | 488 | 496 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 311 | 318 | PF00069 | 0.737 |
DOC_MAPK_RevD_3 | 209 | 225 | PF00069 | 0.603 |
DOC_PP1_RVXF_1 | 384 | 390 | PF00149 | 0.642 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.746 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.551 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.359 |
DOC_PP4_FxxP_1 | 210 | 213 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.583 |
DOC_USP7_UBL2_3 | 400 | 404 | PF12436 | 0.632 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.575 |
DOC_USP7_UBL2_3 | 514 | 518 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 151 | 156 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 311 | 315 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 408 | 412 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 425 | 434 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 440 | 449 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 58 | 67 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 623 | 629 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 658 | 662 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 476 | 493 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 501 | 516 | PF00022 | 0.618 |
LIG_APCC_ABBA_1 | 248 | 253 | PF00400 | 0.665 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.304 |
LIG_BRCT_BRCA1_1 | 444 | 448 | PF00533 | 0.539 |
LIG_CaM_IQ_9 | 473 | 489 | PF13499 | 0.355 |
LIG_EH1_1 | 114 | 122 | PF00400 | 0.531 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.597 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.501 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.490 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.698 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.412 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.782 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.441 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.416 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.447 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.638 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.495 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.735 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.544 |
LIG_LIR_Apic_2 | 189 | 195 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 317 | 326 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 681 | 691 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 626 | 631 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.547 |
LIG_PCNA_TLS_4 | 636 | 643 | PF02747 | 0.617 |
LIG_PDZ_Class_1 | 730 | 735 | PF00595 | 0.450 |
LIG_Pex14_1 | 188 | 192 | PF04695 | 0.555 |
LIG_PTB_Apo_2 | 682 | 689 | PF02174 | 0.579 |
LIG_PTB_Phospho_1 | 682 | 688 | PF10480 | 0.583 |
LIG_RPA_C_Fungi | 53 | 65 | PF08784 | 0.503 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.355 |
LIG_SH2_GRB2like | 13 | 16 | PF00017 | 0.393 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.672 |
LIG_SH2_NCK_1 | 39 | 43 | PF00017 | 0.355 |
LIG_SH2_NCK_1 | 497 | 501 | PF00017 | 0.566 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.678 |
LIG_SH2_SRC | 455 | 458 | PF00017 | 0.292 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.539 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.281 |
LIG_SH2_STAT3 | 716 | 719 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.269 |
LIG_SH3_1 | 224 | 230 | PF00018 | 0.712 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.524 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.671 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.495 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.685 |
LIG_SUMO_SIM_anti_2 | 143 | 148 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 164 | 169 | PF11976 | 0.272 |
LIG_SUMO_SIM_par_1 | 62 | 68 | PF11976 | 0.503 |
LIG_SxIP_EBH_1 | 211 | 225 | PF03271 | 0.609 |
LIG_TRAF2_1 | 644 | 647 | PF00917 | 0.581 |
MOD_CDC14_SPxK_1 | 308 | 311 | PF00782 | 0.515 |
MOD_CDK_SPxK_1 | 305 | 311 | PF00069 | 0.506 |
MOD_CDK_SPxxK_3 | 305 | 312 | PF00069 | 0.508 |
MOD_CDK_SPxxK_3 | 671 | 678 | PF00069 | 0.609 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.348 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.445 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.560 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.666 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.601 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.670 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.338 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.710 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.545 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.756 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.629 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.632 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.452 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.432 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.455 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.550 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.577 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.722 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.598 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.492 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.443 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.419 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.582 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.574 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.473 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.645 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.683 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.749 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.575 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.527 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.536 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.510 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.631 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.520 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.498 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.538 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.559 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.485 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.536 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.484 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.746 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.652 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.546 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.540 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.448 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.301 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.492 |
MOD_OFUCOSY | 262 | 267 | PF10250 | 0.296 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.675 |
MOD_PIKK_1 | 715 | 721 | PF00454 | 0.531 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.369 |
MOD_PKA_1 | 623 | 629 | PF00069 | 0.656 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.492 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.588 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.690 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.398 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.464 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.653 |
MOD_PKA_2 | 657 | 663 | PF00069 | 0.571 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.339 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.772 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.440 |
MOD_Plk_2-3 | 329 | 335 | PF00069 | 0.533 |
MOD_Plk_2-3 | 551 | 557 | PF00069 | 0.765 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.516 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.490 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.466 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.417 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.456 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.618 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.725 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.816 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.632 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.571 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.568 |
MOD_SUMO_rev_2 | 243 | 248 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 509 | 516 | PF00179 | 0.621 |
TRG_DiLeu_BaEn_1 | 322 | 327 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_4 | 562 | 568 | PF01217 | 0.697 |
TRG_DiLeu_BaEn_4 | 589 | 595 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 459 | 464 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 688 | 691 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 622 | 624 | PF00400 | 0.695 |
TRG_Pf-PMV_PEXEL_1 | 462 | 467 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 488 | 492 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 629 | 633 | PF00026 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTI6 | Leptomonas seymouri | 53% | 100% |
A0A3Q8IDU6 | Leishmania donovani | 79% | 100% |
A0A422P3R9 | Trypanosoma rangeli | 27% | 100% |
A4I2G0 | Leishmania infantum | 79% | 100% |
C9ZX37 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AYL3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q8V9 | Leishmania major | 73% | 99% |
V5ATI5 | Trypanosoma cruzi | 26% | 100% |