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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B1D2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0000245 | spliceosomal complex assembly | 7 | 1 |
GO:0007165 | signal transduction | 2 | 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:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0050684 | regulation of mRNA processing | 7 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl 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:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.767 |
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.665 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.733 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.279 |
DEG_SCF_FBW7_1 | 297 | 304 | PF00400 | 0.357 |
DOC_ANK_TNKS_1 | 107 | 114 | PF00023 | 0.667 |
DOC_CKS1_1 | 298 | 303 | PF01111 | 0.357 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.256 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 415 | 424 | PF00069 | 0.264 |
DOC_MAPK_HePTP_8 | 412 | 424 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 415 | 424 | PF00069 | 0.264 |
DOC_PP1_RVXF_1 | 162 | 169 | PF00149 | 0.264 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.724 |
DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.500 |
DOC_PP4_FxxP_1 | 530 | 533 | PF00568 | 0.264 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.599 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.624 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.677 |
DOC_USP7_UBL2_3 | 329 | 333 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.629 |
DOC_USP7_UBL2_3 | 521 | 525 | PF12436 | 0.280 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.267 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 320 | 328 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 671 | 680 | PF00244 | 0.547 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.279 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.669 |
LIG_Clathr_ClatBox_1 | 275 | 279 | PF01394 | 0.279 |
LIG_CtBP_PxDLS_1 | 477 | 481 | PF00389 | 0.279 |
LIG_deltaCOP1_diTrp_1 | 382 | 390 | PF00928 | 0.593 |
LIG_deltaCOP1_diTrp_1 | 433 | 442 | PF00928 | 0.314 |
LIG_EH1_1 | 302 | 310 | PF00400 | 0.430 |
LIG_eIF4E_1 | 202 | 208 | PF01652 | 0.264 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.264 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.609 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.264 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.604 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.616 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.491 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.640 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.558 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.266 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.698 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.515 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.417 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.468 |
LIG_FHA_2 | 734 | 740 | PF00498 | 0.661 |
LIG_Integrin_RGD_1 | 362 | 364 | PF01839 | 0.645 |
LIG_LIR_Apic_2 | 414 | 420 | PF02991 | 0.264 |
LIG_LIR_Apic_2 | 426 | 431 | PF02991 | 0.264 |
LIG_LIR_Apic_2 | 529 | 533 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 183 | 190 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 199 | 208 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 404 | 408 | PF02991 | 0.188 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 503 | 509 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.432 |
LIG_MAD2 | 715 | 723 | PF02301 | 0.538 |
LIG_MYND_3 | 532 | 536 | PF01753 | 0.256 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.264 |
LIG_PTB_Apo_2 | 154 | 161 | PF02174 | 0.420 |
LIG_PTB_Apo_2 | 631 | 638 | PF02174 | 0.549 |
LIG_PTB_Phospho_1 | 154 | 160 | PF10480 | 0.424 |
LIG_PTB_Phospho_1 | 631 | 637 | PF10480 | 0.554 |
LIG_Rb_pABgroove_1 | 237 | 245 | PF01858 | 0.326 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.330 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.264 |
LIG_SH2_CRK | 340 | 344 | PF00017 | 0.426 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.256 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.546 |
LIG_SH2_GRB2like | 491 | 494 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 197 | 201 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 598 | 602 | PF00017 | 0.710 |
LIG_SH2_SRC | 202 | 205 | PF00017 | 0.264 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.525 |
LIG_SUMO_SIM_anti_2 | 283 | 290 | PF11976 | 0.279 |
LIG_SUMO_SIM_anti_2 | 304 | 310 | PF11976 | 0.485 |
LIG_SUMO_SIM_anti_2 | 462 | 471 | PF11976 | 0.264 |
LIG_SUMO_SIM_par_1 | 248 | 255 | PF11976 | 0.264 |
LIG_SUMO_SIM_par_1 | 429 | 436 | PF11976 | 0.256 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.583 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.459 |
LIG_TRAF2_1 | 736 | 739 | PF00917 | 0.623 |
LIG_TYR_ITIM | 504 | 509 | PF00017 | 0.409 |
LIG_UBA3_1 | 305 | 310 | PF00899 | 0.402 |
MOD_CDK_SPK_2 | 297 | 302 | PF00069 | 0.279 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.483 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.409 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.521 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.654 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.717 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.264 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.659 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.707 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.624 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.574 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.714 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.543 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.628 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.409 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.281 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.597 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.303 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.588 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.643 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.551 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.514 |
MOD_CK2_1 | 733 | 739 | PF00069 | 0.661 |
MOD_CMANNOS | 175 | 178 | PF00535 | 0.264 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.507 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.264 |
MOD_GlcNHglycan | 570 | 575 | PF01048 | 0.639 |
MOD_GlcNHglycan | 576 | 581 | PF01048 | 0.652 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.682 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.735 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.736 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.393 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.689 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.534 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.681 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.668 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.579 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.713 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.327 |
MOD_N-GLC_1 | 633 | 638 | PF02516 | 0.547 |
MOD_N-GLC_2 | 219 | 221 | PF02516 | 0.390 |
MOD_N-GLC_2 | 400 | 402 | PF02516 | 0.264 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.725 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.302 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.459 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.264 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.547 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.661 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.474 |
MOD_PIKK_1 | 592 | 598 | PF00454 | 0.615 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.517 |
MOD_PIKK_1 | 704 | 710 | PF00454 | 0.755 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.764 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.704 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.660 |
MOD_PKA_2 | 517 | 523 | PF00069 | 0.167 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.687 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.501 |
MOD_Plk_2-3 | 578 | 584 | PF00069 | 0.608 |
MOD_Plk_2-3 | 586 | 592 | PF00069 | 0.817 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.264 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.280 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.455 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.540 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.593 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.324 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.267 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.426 |
MOD_SUMO_for_1 | 291 | 294 | PF00179 | 0.264 |
MOD_SUMO_rev_2 | 198 | 208 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 285 | 293 | PF00179 | 0.279 |
MOD_SUMO_rev_2 | 325 | 331 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 346 | 351 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 354 | 361 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 55 | 63 | PF00179 | 0.666 |
MOD_SUMO_rev_2 | 599 | 608 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_1 | 347 | 352 | PF01217 | 0.595 |
TRG_DiLeu_BaEn_1 | 668 | 673 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_2 | 525 | 531 | PF01217 | 0.279 |
TRG_DiLeu_BaEn_4 | 628 | 634 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_4 | 675 | 681 | PF01217 | 0.656 |
TRG_DiLeu_LyEn_5 | 668 | 673 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.198 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.167 |
TRG_NLS_Bipartite_1 | 16 | 30 | PF00514 | 0.688 |
TRG_NLS_MonoExtC_3 | 24 | 29 | PF00514 | 0.680 |
TRG_NLS_MonoExtC_3 | 520 | 525 | PF00514 | 0.322 |
TRG_NLS_MonoExtN_4 | 23 | 30 | PF00514 | 0.684 |
TRG_NLS_MonoExtN_4 | 518 | 525 | PF00514 | 0.322 |
TRG_NLS_MonoExtN_4 | 607 | 613 | PF00514 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 499 | 503 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 612 | 617 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 671 | 675 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1H8 | Leptomonas seymouri | 82% | 100% |
A0A0S4JMD1 | Bodo saltans | 55% | 97% |
A0A1X0P1B0 | Trypanosomatidae | 58% | 100% |
A0A3R7KF70 | Trypanosoma rangeli | 59% | 100% |
A0A3S7X404 | Leishmania donovani | 92% | 100% |
A4HIU4 | Leishmania braziliensis | 83% | 99% |
A4I649 | Leishmania infantum | 92% | 100% |
C9ZRG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
Q4Q6T0 | Leishmania major | 94% | 100% |
V5B752 | Trypanosoma cruzi | 61% | 100% |