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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4ICP2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 9 |
GO:0004519 | endonuclease activity | 5 | 9 |
GO:0004521 | RNA endonuclease activity | 5 | 9 |
GO:0004525 | ribonuclease III activity | 6 | 9 |
GO:0004540 | RNA nuclease activity | 4 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 9 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 9 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
GO:0004129 | cytochrome-c oxidase activity | 4 | 1 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 1 |
GO:0009055 | electron transfer activity | 3 | 1 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 1 |
GO:0015078 | proton transmembrane transporter activity | 5 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0015453 | oxidoreduction-driven active transmembrane transporter activity | 5 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
GO:0016675 | oxidoreductase activity, acting on a heme group of donors | 3 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.705 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 111 | 113 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.418 |
DEG_APCC_DBOX_1 | 549 | 557 | PF00400 | 0.505 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.559 |
DOC_CYCLIN_RxL_1 | 150 | 164 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 183 | 189 | PF00069 | 0.659 |
DOC_MAPK_gen_1 | 203 | 213 | PF00069 | 0.261 |
DOC_MAPK_gen_1 | 433 | 440 | PF00069 | 0.641 |
DOC_MAPK_gen_1 | 441 | 447 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 76 | 83 | PF00069 | 0.453 |
DOC_MAPK_HePTP_8 | 158 | 170 | PF00069 | 0.273 |
DOC_MAPK_MEF2A_6 | 161 | 170 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 433 | 440 | PF00069 | 0.631 |
DOC_MAPK_MEF2A_6 | 76 | 85 | PF00069 | 0.456 |
DOC_PP1_RVXF_1 | 327 | 334 | PF00149 | 0.396 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.541 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.553 |
DOC_USP7_MATH_2 | 98 | 104 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 184 | 190 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 25 | 33 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 265 | 270 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 435 | 441 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 451 | 460 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 554 | 564 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 565 | 569 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 573 | 577 | PF00244 | 0.638 |
LIG_Actin_WH2_2 | 373 | 391 | PF00022 | 0.439 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.543 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.492 |
LIG_eIF4E_1 | 136 | 142 | PF01652 | 0.513 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.374 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.596 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.760 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.481 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.466 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.344 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.433 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.432 |
LIG_HP1_1 | 70 | 74 | PF01393 | 0.356 |
LIG_LIR_Apic_2 | 342 | 347 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 162 | 170 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 245 | 253 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 162 | 166 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.479 |
LIG_MAD2 | 25 | 33 | PF02301 | 0.417 |
LIG_MYND_1 | 93 | 97 | PF01753 | 0.513 |
LIG_NRBOX | 327 | 333 | PF00104 | 0.391 |
LIG_Pex14_1 | 205 | 209 | PF04695 | 0.353 |
LIG_Pex14_1 | 339 | 343 | PF04695 | 0.502 |
LIG_PTAP_UEV_1 | 539 | 544 | PF05743 | 0.527 |
LIG_REV1ctd_RIR_1 | 254 | 262 | PF16727 | 0.357 |
LIG_RPA_C_Fungi | 199 | 211 | PF08784 | 0.371 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.422 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.338 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.482 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.551 |
LIG_SH2_NCK_1 | 105 | 109 | PF00017 | 0.770 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.482 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.513 |
LIG_SH3_1 | 421 | 427 | PF00018 | 0.544 |
LIG_SH3_2 | 460 | 465 | PF14604 | 0.583 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.543 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.544 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.633 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.612 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.543 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.585 |
LIG_SUMO_SIM_anti_2 | 164 | 170 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 156 | 162 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 190 | 199 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.390 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.340 |
LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.513 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.510 |
LIG_TRAF2_2 | 97 | 102 | PF00917 | 0.509 |
LIG_UBA3_1 | 210 | 215 | PF00899 | 0.343 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.412 |
LIG_WW_3 | 180 | 184 | PF00397 | 0.455 |
MOD_CDK_SPxK_1 | 259 | 265 | PF00069 | 0.369 |
MOD_CDK_SPxxK_3 | 233 | 240 | PF00069 | 0.442 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.534 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.645 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.376 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.443 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.707 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.678 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.554 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.567 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.490 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.396 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.416 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.535 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.345 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.379 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.423 |
MOD_Cter_Amidation | 35 | 38 | PF01082 | 0.390 |
MOD_Cter_Amidation | 484 | 487 | PF01082 | 0.499 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.512 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.537 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.588 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.483 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.584 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.572 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.643 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.492 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.802 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.545 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.668 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.561 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.489 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.472 |
MOD_N-GLC_1 | 523 | 528 | PF02516 | 0.550 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.659 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.666 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.528 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.374 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.481 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.331 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.277 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.555 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.457 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.468 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.414 |
MOD_NEK2_2 | 173 | 178 | PF00069 | 0.420 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.508 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.507 |
MOD_PKA_1 | 111 | 117 | PF00069 | 0.494 |
MOD_PKA_1 | 183 | 189 | PF00069 | 0.498 |
MOD_PKA_1 | 404 | 410 | PF00069 | 0.530 |
MOD_PKA_1 | 487 | 493 | PF00069 | 0.469 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.605 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.498 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.489 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.530 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.578 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.663 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.592 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.703 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.377 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.355 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.495 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.358 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.513 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.377 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.447 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.369 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.612 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.612 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.542 |
MOD_SUMO_rev_2 | 322 | 331 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 63 | 70 | PF00179 | 0.355 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.387 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 424 | 429 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 566 | 571 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.552 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 202 | 204 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 464 | 466 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 578 | 580 | PF00400 | 0.694 |
TRG_NLS_Bipartite_1 | 433 | 454 | PF00514 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7V7 | Leptomonas seymouri | 39% | 93% |
A0A1X0P8F1 | Trypanosomatidae | 34% | 90% |
A0A3S7XAF0 | Leishmania donovani | 100% | 100% |
A0A422MWV0 | Trypanosoma rangeli | 35% | 98% |
E9AIX5 | Leishmania braziliensis | 77% | 100% |
E9ASL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q1Y4 | Leishmania major | 93% | 100% |