Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0034399 | nuclear periphery | 2 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0097165 | nuclear stress granule | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4HPB9
Term | Name | Level | Count |
---|---|---|---|
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902775 | mitochondrial large ribosomal subunit assembly | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 22 |
GO:0003676 | nucleic acid binding | 3 | 22 |
GO:0003824 | catalytic activity | 1 | 22 |
GO:0004386 | helicase activity | 2 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0005524 | ATP binding | 5 | 22 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0030554 | adenyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 22 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
GO:0003724 | RNA helicase activity | 3 | 5 |
GO:0003743 | translation initiation factor activity | 4 | 4 |
GO:0008135 | translation factor activity, RNA binding | 3 | 4 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 5 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0045182 | translation regulator activity | 1 | 4 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 4 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0003723 | RNA binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.798 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.714 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 97 | 99 | PF00082 | 0.742 |
CLV_PCSK_PC7_1 | 280 | 286 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 639 | 643 | PF00082 | 0.358 |
DEG_APCC_DBOX_1 | 339 | 347 | PF00400 | 0.485 |
DEG_APCC_DBOX_1 | 434 | 442 | PF00400 | 0.398 |
DEG_APCC_DBOX_1 | 492 | 500 | PF00400 | 0.527 |
DEG_SPOP_SBC_1 | 214 | 218 | PF00917 | 0.381 |
DOC_CYCLIN_RxL_1 | 407 | 416 | PF00134 | 0.439 |
DOC_CYCLIN_RxL_1 | 425 | 433 | PF00134 | 0.572 |
DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 15 | 21 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 654 | 657 | PF00134 | 0.409 |
DOC_MAPK_gen_1 | 280 | 289 | PF00069 | 0.467 |
DOC_MAPK_JIP1_4 | 407 | 413 | PF00069 | 0.444 |
DOC_PP1_RVXF_1 | 495 | 502 | PF00149 | 0.434 |
DOC_PP1_RVXF_1 | 509 | 515 | PF00149 | 0.293 |
DOC_PP1_RVXF_1 | 524 | 531 | PF00149 | 0.515 |
DOC_PP1_RVXF_1 | 586 | 593 | PF00149 | 0.433 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 654 | 657 | PF13499 | 0.409 |
DOC_PP4_FxxP_1 | 265 | 268 | PF00568 | 0.503 |
DOC_PP4_FxxP_1 | 632 | 635 | PF00568 | 0.331 |
DOC_PP4_FxxP_1 | 676 | 679 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 573 | 581 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 626 | 631 | PF00244 | 0.311 |
LIG_Actin_WH2_2 | 66 | 84 | PF00022 | 0.515 |
LIG_AP2alpha_1 | 667 | 671 | PF02296 | 0.531 |
LIG_APCC_ABBA_1 | 246 | 251 | PF00400 | 0.528 |
LIG_BIR_III_4 | 120 | 124 | PF00653 | 0.542 |
LIG_BIR_III_4 | 50 | 54 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.372 |
LIG_EH1_1 | 324 | 332 | PF00400 | 0.431 |
LIG_eIF4E_1 | 194 | 200 | PF01652 | 0.528 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.411 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.465 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.484 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.463 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.471 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.692 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.520 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.381 |
LIG_Integrin_RGD_1 | 619 | 621 | PF01839 | 0.181 |
LIG_IRF3_LxIS_1 | 248 | 255 | PF10401 | 0.389 |
LIG_LIR_Apic_2 | 263 | 268 | PF02991 | 0.503 |
LIG_LIR_Apic_2 | 629 | 635 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 674 | 679 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 433 | 441 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 629 | 638 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 666 | 675 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 9 | 20 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 176 | 180 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.739 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 591 | 595 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 629 | 633 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 666 | 670 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.499 |
LIG_NRBOX | 198 | 204 | PF00104 | 0.485 |
LIG_OCRL_FandH_1 | 317 | 329 | PF00620 | 0.431 |
LIG_PCNA_PIPBox_1 | 707 | 716 | PF02747 | 0.549 |
LIG_PCNA_yPIPBox_3 | 148 | 161 | PF02747 | 0.319 |
LIG_Pex14_2 | 667 | 671 | PF04695 | 0.531 |
LIG_PTB_Apo_2 | 670 | 677 | PF02174 | 0.547 |
LIG_SH2_CRK | 114 | 118 | PF00017 | 0.481 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.569 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.489 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.328 |
LIG_SH2_CRK | 601 | 605 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 601 | 605 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 628 | 632 | PF00017 | 0.242 |
LIG_SH2_STAT3 | 647 | 650 | PF00017 | 0.458 |
LIG_SH2_STAT3 | 662 | 665 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.554 |
LIG_SH3_1 | 41 | 47 | PF00018 | 0.519 |
LIG_SH3_2 | 679 | 684 | PF14604 | 0.579 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.382 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.557 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.539 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.474 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.499 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.549 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.549 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.519 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.702 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.535 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.683 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.587 |
LIG_SUMO_SIM_par_1 | 115 | 120 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 437 | 443 | PF11976 | 0.381 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.445 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.528 |
LIG_TYR_ITIM | 420 | 425 | PF00017 | 0.422 |
LIG_UBA3_1 | 199 | 205 | PF00899 | 0.528 |
LIG_UBA3_1 | 360 | 368 | PF00899 | 0.444 |
LIG_UBA3_1 | 397 | 403 | PF00899 | 0.424 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.431 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.464 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.431 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.827 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.626 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.435 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.668 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.513 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.485 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.507 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.453 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.441 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.448 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.579 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.431 |
MOD_GlcNHglycan | 222 | 226 | PF01048 | 0.302 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.277 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.724 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.580 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.550 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.506 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.481 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.477 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.491 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.792 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.677 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.598 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.698 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.437 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.487 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.490 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.328 |
MOD_N-GLC_1 | 671 | 676 | PF02516 | 0.515 |
MOD_N-GLC_1 | 689 | 694 | PF02516 | 0.552 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.440 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.494 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.475 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.417 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.543 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.527 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.474 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.457 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.537 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.480 |
MOD_NEK2_2 | 628 | 633 | PF00069 | 0.314 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.695 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.372 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.437 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.392 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.431 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.719 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.540 |
MOD_PK_1 | 98 | 104 | PF00069 | 0.563 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.563 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.381 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.472 |
MOD_PKA_2 | 696 | 702 | PF00069 | 0.652 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.589 |
MOD_PKB_1 | 624 | 632 | PF00069 | 0.289 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.509 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.507 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.426 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.490 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.521 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.515 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.431 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.439 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.511 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.360 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.479 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.475 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.514 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.338 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.484 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.747 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.684 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.508 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.441 |
TRG_DiLeu_BaEn_1 | 298 | 303 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 407 | 412 | PF01217 | 0.436 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 700 | 702 | PF00400 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 319 | 324 | PF00026 | 0.341 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I458 | Leptomonas seymouri | 73% | 100% |
A0A0N1I5R1 | Leptomonas seymouri | 20% | 90% |
A0A0S4IX79 | Bodo saltans | 23% | 98% |
A0A0S4JPF4 | Bodo saltans | 38% | 100% |
A0A1X0P7J3 | Trypanosomatidae | 56% | 100% |
A0A3Q8ID91 | Leishmania donovani | 26% | 100% |
A0A3Q8IF94 | Leishmania donovani | 24% | 100% |
A0A3Q8IG57 | Leishmania donovani | 86% | 92% |
A4HGR1 | Leishmania braziliensis | 26% | 100% |
A4I3T6 | Leishmania infantum | 26% | 100% |
A4I7K4 | Leishmania infantum | 24% | 100% |
A4ICF9 | Leishmania infantum | 88% | 100% |
D0A3C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AT30 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B2G1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q1G8 | Leishmania major | 87% | 100% |
Q4Q5P5 | Leishmania major | 24% | 100% |
Q4Q858 | Leishmania major | 26% | 100% |
V5D8J9 | Trypanosoma cruzi | 56% | 100% |