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: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: A4HMD7
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.266 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 833 | 835 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 846 | 848 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 846 | 848 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.382 |
DEG_SPOP_SBC_1 | 139 | 143 | PF00917 | 0.380 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.680 |
DOC_AGCK_PIF_2 | 124 | 129 | PF00069 | 0.293 |
DOC_CYCLIN_RxL_1 | 393 | 403 | PF00134 | 0.254 |
DOC_CYCLIN_RxL_1 | 470 | 478 | PF00134 | 0.254 |
DOC_MAPK_gen_1 | 244 | 253 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 348 | 355 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 587 | 596 | PF00069 | 0.228 |
DOC_PP1_RVXF_1 | 452 | 458 | PF00149 | 0.496 |
DOC_PP1_RVXF_1 | 630 | 637 | PF00149 | 0.279 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.517 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.495 |
DOC_SPAK_OSR1_1 | 67 | 71 | PF12202 | 0.385 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.392 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.372 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.189 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 669 | 674 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.344 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 290 | 294 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 546 | 551 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 587 | 595 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.250 |
LIG_14-3-3_CanoR_1 | 649 | 653 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 706 | 712 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 740 | 744 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.279 |
LIG_AP2alpha_2 | 104 | 106 | PF02296 | 0.279 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.380 |
LIG_deltaCOP1_diTrp_1 | 422 | 427 | PF00928 | 0.223 |
LIG_eIF4E_1 | 450 | 456 | PF01652 | 0.384 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.366 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.276 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.606 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.383 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.427 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.416 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.206 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.313 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.601 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.551 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.277 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.430 |
LIG_LIR_Apic_2 | 385 | 390 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 803 | 807 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 121 | 130 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 206 | 215 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 235 | 243 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 422 | 433 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 619 | 628 | PF02991 | 0.252 |
LIG_LIR_Gen_1 | 686 | 692 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 710 | 720 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 761 | 771 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.216 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 619 | 623 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 686 | 690 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 710 | 715 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 761 | 766 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 768 | 774 | PF02991 | 0.300 |
LIG_LYPXL_yS_3 | 144 | 147 | PF13949 | 0.310 |
LIG_MLH1_MIPbox_1 | 120 | 124 | PF16413 | 0.380 |
LIG_NRBOX | 331 | 337 | PF00104 | 0.382 |
LIG_NRBOX | 442 | 448 | PF00104 | 0.173 |
LIG_PCNA_PIPBox_1 | 610 | 619 | PF02747 | 0.244 |
LIG_PCNA_yPIPBox_3 | 603 | 617 | PF02747 | 0.248 |
LIG_PCNA_yPIPBox_3 | 624 | 637 | PF02747 | 0.165 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.279 |
LIG_Pex14_1 | 637 | 641 | PF04695 | 0.268 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.477 |
LIG_Pex14_2 | 103 | 107 | PF04695 | 0.258 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.215 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.625 |
LIG_PTB_Apo_2 | 706 | 713 | PF02174 | 0.317 |
LIG_PTB_Phospho_1 | 706 | 712 | PF10480 | 0.313 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.189 |
LIG_SH2_CRK | 771 | 775 | PF00017 | 0.290 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.293 |
LIG_SH2_PTP2 | 269 | 272 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 687 | 690 | PF00017 | 0.283 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 767 | 771 | PF00017 | 0.361 |
LIG_SH2_STAT3 | 639 | 642 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 616 | 619 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.345 |
LIG_SH3_2 | 62 | 67 | PF14604 | 0.460 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.375 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.569 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.343 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.202 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.480 |
LIG_SH3_3 | 714 | 720 | PF00018 | 0.395 |
LIG_SH3_3 | 787 | 793 | PF00018 | 0.364 |
LIG_SH3_3 | 794 | 800 | PF00018 | 0.380 |
LIG_SUMO_SIM_anti_2 | 439 | 445 | PF11976 | 0.165 |
LIG_SUMO_SIM_anti_2 | 472 | 478 | PF11976 | 0.208 |
LIG_SUMO_SIM_par_1 | 439 | 445 | PF11976 | 0.224 |
LIG_SUMO_SIM_par_1 | 472 | 478 | PF11976 | 0.208 |
LIG_SxIP_EBH_1 | 203 | 216 | PF03271 | 0.349 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.490 |
LIG_TYR_ITSM | 233 | 240 | PF00017 | 0.316 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.185 |
LIG_WRC_WIRS_1 | 829 | 834 | PF05994 | 0.331 |
MOD_CDC14_SPxK_1 | 321 | 324 | PF00782 | 0.380 |
MOD_CDK_SPK_2 | 624 | 629 | PF00069 | 0.185 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.279 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.493 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.492 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.547 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.355 |
MOD_CK1_1 | 783 | 789 | PF00069 | 0.334 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.606 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.246 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.517 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.406 |
MOD_CK2_1 | 836 | 842 | PF00069 | 0.382 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.528 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.532 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.569 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.293 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.302 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.610 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.568 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.422 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.349 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.521 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.211 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.297 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.249 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.554 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.288 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.273 |
MOD_N-GLC_1 | 647 | 652 | PF02516 | 0.466 |
MOD_N-GLC_1 | 780 | 785 | PF02516 | 0.529 |
MOD_N-GLC_2 | 169 | 171 | PF02516 | 0.435 |
MOD_N-GLC_2 | 224 | 226 | PF02516 | 0.479 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.279 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.362 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.355 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.213 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.276 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.249 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.296 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.324 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.205 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.389 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.384 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.381 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.409 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.325 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.305 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.316 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.762 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.461 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.192 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.417 |
MOD_PK_1 | 89 | 95 | PF00069 | 0.314 |
MOD_PKA_1 | 524 | 530 | PF00069 | 0.408 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.515 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.531 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.477 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.464 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.235 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.294 |
MOD_PKA_2 | 648 | 654 | PF00069 | 0.268 |
MOD_PKA_2 | 739 | 745 | PF00069 | 0.370 |
MOD_PKB_1 | 364 | 372 | PF00069 | 0.512 |
MOD_Plk_1 | 647 | 653 | PF00069 | 0.277 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.279 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.316 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.423 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.423 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.342 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.339 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.274 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.270 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.276 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.364 |
MOD_Plk_4 | 707 | 713 | PF00069 | 0.303 |
MOD_Plk_4 | 739 | 745 | PF00069 | 0.362 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.270 |
MOD_Plk_4 | 800 | 806 | PF00069 | 0.403 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.279 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.189 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.232 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.268 |
MOD_ProDKin_1 | 669 | 675 | PF00069 | 0.313 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.340 |
TRG_DiLeu_BaEn_1 | 676 | 681 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.282 |
TRG_DiLeu_BaLyEn_6 | 589 | 594 | PF01217 | 0.160 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.189 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 712 | 715 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.293 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 355 | 358 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 732 | 735 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 845 | 847 | PF00400 | 0.365 |
TRG_NES_CRM1_1 | 327 | 342 | PF08389 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 539 | 543 | PF00026 | 0.177 |
TRG_Pf-PMV_PEXEL_1 | 89 | 94 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 50% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 55% | 100% |
A0A3Q8IHT0 | Leishmania donovani | 71% | 99% |
A0A3Q8II34 | Leishmania donovani | 55% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 71% | 100% |
A0A3Q8IV37 | Leishmania donovani | 81% | 100% |
A0A422MX14 | Trypanosoma rangeli | 56% | 100% |
A4HFF9 | Leishmania braziliensis | 70% | 99% |
A4HMD5 | Leishmania braziliensis | 74% | 99% |
A4HMD6 | Leishmania braziliensis | 58% | 100% |
A4IB08 | Leishmania infantum | 70% | 99% |
A4IB09 | Leishmania infantum | 71% | 100% |
A4IB10 | Leishmania infantum | 55% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E2RG47 | Canis lupus familiaris | 29% | 100% |
E9AET6 | Leishmania major | 66% | 99% |
E9AET7 | Leishmania major | 71% | 100% |
E9AET8 | Leishmania major | 55% | 100% |
E9AET9 | Leishmania major | 80% | 100% |
E9AHU4 | Leishmania infantum | 81% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 99% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P46975 | Caenorhabditis elegans | 31% | 100% |
P46977 | Homo sapiens | 29% | 100% |
P46978 | Mus musculus | 29% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 29% | 100% |
Q54NM9 | Dictyostelium discoideum | 30% | 100% |
Q5RCE2 | Pongo abelii | 29% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 29% | 100% |
Q93ZY3 | Arabidopsis thaliana | 31% | 100% |
Q9FX21 | Arabidopsis thaliana | 30% | 100% |
V5BDM6 | Trypanosoma cruzi | 57% | 100% |