Intracellular protein trafficking, GTP-binding
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4I9C0
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003746 | translation elongation factor activity | 4 | 8 |
GO:0008135 | translation factor activity, RNA binding | 3 | 8 |
GO:0045182 | translation regulator activity | 1 | 8 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.473 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 713 | 715 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 827 | 829 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.580 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 709 | 711 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 709 | 711 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 796 | 800 | PF00082 | 0.306 |
CLV_Separin_Metazoa | 770 | 774 | PF03568 | 0.437 |
DEG_SCF_TRCP1_1 | 250 | 256 | PF00400 | 0.335 |
DEG_SCF_TRCP1_1 | 366 | 371 | PF00400 | 0.437 |
DEG_SPOP_SBC_1 | 329 | 333 | PF00917 | 0.650 |
DOC_ANK_TNKS_1 | 802 | 809 | PF00023 | 0.448 |
DOC_CKS1_1 | 472 | 477 | PF01111 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 537 | 543 | PF00134 | 0.437 |
DOC_CYCLIN_yCln2_LP_2 | 835 | 841 | PF00134 | 0.544 |
DOC_MAPK_gen_1 | 525 | 535 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 580 | 587 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 714 | 720 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 800 | 809 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 528 | 537 | PF00069 | 0.437 |
DOC_MAPK_NFAT4_5 | 528 | 536 | PF00069 | 0.448 |
DOC_MAPK_RevD_3 | 609 | 625 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 794 | 800 | PF00149 | 0.554 |
DOC_PP2B_LxvP_1 | 537 | 540 | PF13499 | 0.460 |
DOC_PP2B_LxvP_1 | 567 | 570 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 835 | 838 | PF13499 | 0.533 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.414 |
DOC_USP7_UBL2_3 | 826 | 830 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.675 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 496 | 505 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 759 | 767 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 484 | 501 | PF00022 | 0.437 |
LIG_Actin_WH2_2 | 760 | 775 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 105 | 110 | PF00400 | 0.372 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.542 |
LIG_BIR_III_2 | 549 | 553 | PF00653 | 0.523 |
LIG_BRCT_BRCA1_1 | 640 | 644 | PF00533 | 0.389 |
LIG_EVH1_2 | 725 | 729 | PF00568 | 0.339 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.574 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.451 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.623 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.438 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.450 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.546 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.437 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.546 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.376 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.363 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.382 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.437 |
LIG_FHA_1 | 809 | 815 | PF00498 | 0.437 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.556 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.485 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.392 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.437 |
LIG_FHA_2 | 621 | 627 | PF00498 | 0.440 |
LIG_GBD_Chelix_1 | 166 | 174 | PF00786 | 0.437 |
LIG_GBD_Chelix_1 | 531 | 539 | PF00786 | 0.339 |
LIG_LIR_Gen_1 | 511 | 519 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 511 | 515 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 672 | 677 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 728 | 732 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 746 | 752 | PF02991 | 0.562 |
LIG_MLH1_MIPbox_1 | 640 | 644 | PF16413 | 0.389 |
LIG_PCNA_yPIPBox_3 | 92 | 104 | PF02747 | 0.406 |
LIG_Rb_pABgroove_1 | 483 | 491 | PF01858 | 0.437 |
LIG_SH2_CRK | 423 | 427 | PF00017 | 0.504 |
LIG_SH2_CRK | 512 | 516 | PF00017 | 0.440 |
LIG_SH2_CRK | 594 | 598 | PF00017 | 0.483 |
LIG_SH2_NCK_1 | 196 | 200 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 489 | 493 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 594 | 598 | PF00017 | 0.483 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.628 |
LIG_SH2_SRC | 749 | 752 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 594 | 598 | PF00017 | 0.396 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 766 | 769 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.462 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.642 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 141 | 147 | PF11976 | 0.522 |
LIG_SUMO_SIM_anti_2 | 735 | 740 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 482 | 490 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 678 | 684 | PF11976 | 0.478 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.418 |
LIG_TRAF2_2 | 48 | 53 | PF00917 | 0.515 |
LIG_TYR_ITIM | 421 | 426 | PF00017 | 0.417 |
LIG_TYR_ITIM | 592 | 597 | PF00017 | 0.339 |
LIG_UBA3_1 | 566 | 574 | PF00899 | 0.312 |
MOD_CDK_SPK_2 | 471 | 476 | PF00069 | 0.326 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.697 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.683 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.298 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.297 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.296 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.347 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.651 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.296 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.651 |
MOD_CK2_1 | 403 | 409 | PF00069 | 0.292 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.384 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.481 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.610 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.640 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.552 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.593 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.423 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.580 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.600 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.309 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.428 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.390 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.376 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.315 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.235 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.314 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.672 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.322 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.399 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.700 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.640 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.580 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.718 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.718 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.324 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.277 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.367 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.291 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.624 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.414 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.391 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.303 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.290 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.724 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.681 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.288 |
MOD_N-GLC_1 | 604 | 609 | PF02516 | 0.289 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.434 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.388 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.410 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.293 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.312 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.472 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.529 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.297 |
MOD_NEK2_2 | 466 | 471 | PF00069 | 0.302 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.502 |
MOD_PIKK_1 | 654 | 660 | PF00454 | 0.337 |
MOD_PK_1 | 403 | 409 | PF00069 | 0.278 |
MOD_PK_1 | 709 | 715 | PF00069 | 0.505 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.531 |
MOD_PKA_1 | 709 | 715 | PF00069 | 0.424 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.570 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.410 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.295 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.372 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.302 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.464 |
MOD_PKA_2 | 758 | 764 | PF00069 | 0.274 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.598 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.527 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.323 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.368 |
MOD_Plk_1 | 583 | 589 | PF00069 | 0.410 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.364 |
MOD_Plk_1 | 663 | 669 | PF00069 | 0.429 |
MOD_Plk_1 | 775 | 781 | PF00069 | 0.294 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.553 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.627 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.519 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.619 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.289 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.358 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.293 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.254 |
MOD_Plk_4 | 639 | 645 | PF00069 | 0.404 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.344 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.426 |
MOD_Plk_4 | 725 | 731 | PF00069 | 0.324 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.646 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.763 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.788 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.652 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.427 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.274 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.663 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.447 |
MOD_SUMO_for_1 | 705 | 708 | PF00179 | 0.395 |
TRG_DiLeu_BaEn_1 | 255 | 260 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 793 | 798 | PF01217 | 0.350 |
TRG_DiLeu_BaEn_1 | 816 | 821 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.549 |
TRG_DiLeu_LyEn_5 | 793 | 798 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 749 | 752 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 579 | 581 | PF00400 | 0.295 |
TRG_NLS_Bipartite_1 | 153 | 175 | PF00514 | 0.434 |
TRG_NLS_MonoExtC_3 | 827 | 833 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 826 | 832 | PF00514 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K5 | Leptomonas seymouri | 68% | 100% |
A0A0S4JM58 | Bodo saltans | 52% | 100% |
A0A1X0NRK6 | Trypanosomatidae | 47% | 97% |
A0A3R7MHD3 | Trypanosoma rangeli | 50% | 100% |
A0A3S7X775 | Leishmania donovani | 100% | 100% |
A4HLZ0 | Leishmania braziliensis | 84% | 100% |
C9ZJA2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9B4B9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
Q4Q3Q6 | Leishmania major | 93% | 100% |
V5BF52 | Trypanosoma cruzi | 50% | 99% |