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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
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: E9B5B5
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031848 | protection from non-homologous end joining at telomere | 6 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0036297 | interstrand cross-link repair | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043247 | telomere maintenance in response to DNA damage | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0035312 | 5'-3' DNA exonuclease activity | 7 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.441 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.584 |
CLV_C14_Caspase3-7 | 556 | 560 | PF00656 | 0.527 |
CLV_MEL_PAP_1 | 512 | 518 | PF00089 | 0.509 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 540 | 542 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 589 | 591 | PF00675 | 0.674 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 591 | 593 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 630 | 632 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.233 |
CLV_Separin_Metazoa | 186 | 190 | PF03568 | 0.464 |
DEG_APCC_DBOX_1 | 154 | 162 | PF00400 | 0.386 |
DEG_APCC_DBOX_1 | 639 | 647 | PF00400 | 0.708 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.348 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.463 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.366 |
DOC_CYCLIN_RxL_1 | 150 | 159 | PF00134 | 0.389 |
DOC_MAPK_gen_1 | 211 | 220 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 227 | 234 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 155 | 162 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.581 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.436 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.346 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.347 |
DOC_PP4_FxxP_1 | 483 | 486 | PF00568 | 0.436 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.332 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.749 |
DOC_USP7_UBL2_3 | 542 | 546 | PF12436 | 0.715 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 634 | 639 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.391 |
LIG_14-3-3_CanoR_1 | 104 | 108 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 265 | 269 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 465 | 474 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 524 | 529 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 580 | 586 | PF00244 | 0.483 |
LIG_BIR_III_2 | 236 | 240 | PF00653 | 0.473 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.336 |
LIG_deltaCOP1_diTrp_1 | 92 | 97 | PF00928 | 0.401 |
LIG_EH1_1 | 52 | 60 | PF00400 | 0.214 |
LIG_EVH1_2 | 134 | 138 | PF00568 | 0.267 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.378 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.436 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.588 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.610 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.714 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.670 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.531 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.543 |
LIG_Integrin_isoDGR_2 | 102 | 104 | PF01839 | 0.380 |
LIG_LIR_Apic_2 | 106 | 110 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 164 | 170 | PF02991 | 0.329 |
LIG_LIR_Apic_2 | 398 | 403 | PF02991 | 0.389 |
LIG_LIR_Apic_2 | 482 | 486 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 435 | 445 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 458 | 468 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 479 | 487 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 523 | 534 | PF02991 | 0.659 |
LIG_LIR_Gen_1 | 623 | 634 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 92 | 98 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 479 | 483 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.489 |
LIG_MYND_1 | 327 | 331 | PF01753 | 0.419 |
LIG_NRBOX | 157 | 163 | PF00104 | 0.323 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.238 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.467 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.416 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.442 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.432 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.492 |
LIG_SH2_CRK | 437 | 441 | PF00017 | 0.531 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.504 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 501 | 505 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.302 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.529 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.466 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.501 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.467 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.583 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.370 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.571 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.579 |
LIG_SUMO_SIM_anti_2 | 159 | 164 | PF11976 | 0.319 |
LIG_SUMO_SIM_anti_2 | 438 | 444 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 159 | 164 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 330 | 336 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 438 | 444 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 662 | 670 | PF11976 | 0.581 |
LIG_TRAF2_1 | 570 | 573 | PF00917 | 0.507 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.335 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.230 |
LIG_WW_2 | 109 | 112 | PF00397 | 0.411 |
MOD_CDC14_SPxK_1 | 273 | 276 | PF00782 | 0.355 |
MOD_CDC14_SPxK_1 | 637 | 640 | PF00782 | 0.579 |
MOD_CDK_SPxK_1 | 270 | 276 | PF00069 | 0.329 |
MOD_CDK_SPxK_1 | 634 | 640 | PF00069 | 0.578 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.489 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.656 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.631 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.637 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.671 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.630 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.676 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.471 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.353 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.696 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.393 |
MOD_Cter_Amidation | 538 | 541 | PF01082 | 0.482 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.779 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.712 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.573 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.657 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.379 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.369 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.714 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.690 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.641 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.345 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.510 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.660 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.673 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.620 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.319 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.590 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.596 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.416 |
MOD_N-GLC_2 | 14 | 16 | PF02516 | 0.270 |
MOD_N-GLC_2 | 61 | 63 | PF02516 | 0.344 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.298 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.232 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.545 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.520 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.331 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.681 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.620 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.382 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.454 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.471 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.635 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.189 |
MOD_PIKK_1 | 592 | 598 | PF00454 | 0.516 |
MOD_PK_1 | 524 | 530 | PF00069 | 0.642 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.322 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.560 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.731 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.544 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.421 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.450 |
MOD_PKB_1 | 590 | 598 | PF00069 | 0.468 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.546 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.296 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.486 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.527 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.324 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.363 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.273 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.481 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.333 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.474 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.358 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.747 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.512 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.730 |
MOD_ProDKin_1 | 634 | 640 | PF00069 | 0.777 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.395 |
MOD_SUMO_rev_2 | 543 | 548 | PF00179 | 0.577 |
TRG_DiLeu_BaEn_1 | 392 | 397 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_2 | 475 | 481 | PF01217 | 0.271 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 510 | 513 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 640 | 643 | PF00400 | 0.538 |
TRG_NLS_MonoExtC_3 | 589 | 594 | PF00514 | 0.782 |
TRG_NLS_MonoExtN_4 | 590 | 595 | PF00514 | 0.780 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB91 | Leptomonas seymouri | 42% | 77% |
A0A1X0P9Y1 | Trypanosomatidae | 32% | 90% |
A0A3Q8IHR3 | Leishmania donovani | 85% | 100% |
A0A3R7MJM0 | Trypanosoma rangeli | 31% | 94% |
A4HB44 | Leishmania braziliensis | 66% | 98% |
A4IA93 | Leishmania infantum | 85% | 83% |
C9ZM02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 93% |
Q4Q2L8 | Leishmania major | 85% | 99% |
V5BQH0 | Trypanosoma cruzi | 34% | 94% |