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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HNF6
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 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:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018095 | protein polyglutamylation | 7 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018200 | peptidyl-glutamic acid modification | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 5 |
GO:0016874 | ligase activity | 2 | 11 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 5 |
GO:0016881 | acid-amino acid ligase activity | 4 | 5 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 5 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 1 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.620 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.243 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 696 | 698 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.687 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.689 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.408 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.399 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.470 |
DOC_CKS1_1 | 348 | 353 | PF01111 | 0.531 |
DOC_CYCLIN_RxL_1 | 168 | 175 | PF00134 | 0.575 |
DOC_CYCLIN_RxL_1 | 633 | 642 | PF00134 | 0.496 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 548 | 557 | PF00134 | 0.520 |
DOC_MAPK_FxFP_2 | 188 | 191 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 170 | 176 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 404 | 410 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 554 | 562 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 220 | 227 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 554 | 562 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 626 | 634 | PF00069 | 0.327 |
DOC_MAPK_NFAT4_5 | 220 | 228 | PF00069 | 0.448 |
DOC_PP2B_LxvP_1 | 44 | 47 | PF13499 | 0.639 |
DOC_PP2B_PxIxI_1 | 353 | 359 | PF00149 | 0.470 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.658 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.728 |
DOC_PP4_FxxP_1 | 188 | 191 | PF00568 | 0.461 |
DOC_PP4_FxxP_1 | 331 | 334 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 643 | 646 | PF00568 | 0.490 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.561 |
DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.508 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 263 | 271 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 278 | 282 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 488 | 498 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 503 | 512 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 637 | 646 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 76 | 81 | PF00244 | 0.660 |
LIG_Actin_RPEL_3 | 572 | 591 | PF02755 | 0.486 |
LIG_Actin_WH2_2 | 247 | 265 | PF00022 | 0.461 |
LIG_APCC_ABBA_1 | 422 | 427 | PF00400 | 0.445 |
LIG_APCC_ABBAyCdc20_2 | 421 | 427 | PF00400 | 0.445 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.695 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.394 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.501 |
LIG_Clathr_ClatBox_1 | 542 | 546 | PF01394 | 0.531 |
LIG_deltaCOP1_diTrp_1 | 478 | 486 | PF00928 | 0.486 |
LIG_eIF4E_1 | 394 | 400 | PF01652 | 0.506 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.652 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.573 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.605 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.485 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.744 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.470 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.646 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.445 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.592 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.650 |
LIG_LIR_Apic_2 | 101 | 105 | PF02991 | 0.650 |
LIG_LIR_Apic_2 | 13 | 18 | PF02991 | 0.712 |
LIG_LIR_Apic_2 | 187 | 191 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 330 | 334 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 641 | 646 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 321 | 332 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 515 | 524 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 515 | 519 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 685 | 690 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.626 |
LIG_LYPXL_yS_3 | 85 | 88 | PF13949 | 0.617 |
LIG_MLH1_MIPbox_1 | 186 | 190 | PF16413 | 0.412 |
LIG_MYND_1 | 53 | 57 | PF01753 | 0.689 |
LIG_NRBOX | 580 | 586 | PF00104 | 0.384 |
LIG_Pex14_1 | 81 | 85 | PF04695 | 0.405 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.337 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.445 |
LIG_RPA_C_Fungi | 112 | 124 | PF08784 | 0.718 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.313 |
LIG_SH2_CRK | 411 | 415 | PF00017 | 0.313 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.722 |
LIG_SH2_SRC | 194 | 197 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 664 | 668 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 502 | 505 | PF00017 | 0.192 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.604 |
LIG_SH3_1 | 374 | 380 | PF00018 | 0.332 |
LIG_SH3_2 | 348 | 353 | PF14604 | 0.418 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.467 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.405 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.313 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.629 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.605 |
LIG_SUMO_SIM_par_1 | 129 | 134 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 657 | 663 | PF11976 | 0.342 |
LIG_TRAF2_2 | 440 | 445 | PF00917 | 0.418 |
LIG_UBA3_1 | 355 | 360 | PF00899 | 0.332 |
LIG_WRC_WIRS_1 | 414 | 419 | PF05994 | 0.332 |
LIG_WRC_WIRS_1 | 513 | 518 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 640 | 645 | PF05994 | 0.487 |
MOD_CDK_SPxK_1 | 347 | 353 | PF00069 | 0.418 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.706 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.500 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.589 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.655 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.414 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.719 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.516 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.563 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.418 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.610 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.313 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.439 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.573 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.367 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.312 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.438 |
MOD_Cter_Amidation | 302 | 305 | PF01082 | 0.298 |
MOD_Cter_Amidation | 402 | 405 | PF01082 | 0.313 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.698 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.464 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.469 |
MOD_GlcNHglycan | 533 | 537 | PF01048 | 0.360 |
MOD_GlcNHglycan | 703 | 706 | PF01048 | 0.412 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.649 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.446 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.596 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.605 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.645 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.508 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.553 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.323 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.659 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.259 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.580 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.538 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.536 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.298 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.696 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.192 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.537 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.387 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.602 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.632 |
MOD_PKA_1 | 277 | 283 | PF00069 | 0.473 |
MOD_PKA_1 | 594 | 600 | PF00069 | 0.622 |
MOD_PKA_1 | 76 | 82 | PF00069 | 0.657 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.676 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.376 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.507 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.325 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.486 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.622 |
MOD_PKA_2 | 695 | 701 | PF00069 | 0.463 |
MOD_PKB_1 | 115 | 123 | PF00069 | 0.716 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.690 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.524 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.307 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.267 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.540 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.557 |
MOD_Plk_2-3 | 470 | 476 | PF00069 | 0.332 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.400 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.418 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.519 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.491 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.298 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.568 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.393 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.343 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.304 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.524 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.445 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.403 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.645 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 553 | 558 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 635 | 640 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.617 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 593 | 595 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 695 | 697 | PF00400 | 0.431 |
TRG_NLS_MonoExtN_4 | 73 | 80 | PF00514 | 0.615 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAP5 | Leptomonas seymouri | 75% | 97% |
A0A0S4J7C9 | Bodo saltans | 51% | 100% |
A0A0S4KQK8 | Bodo saltans | 35% | 100% |
A0A1X0NXX8 | Trypanosomatidae | 30% | 99% |
A0A1X0P6A0 | Trypanosomatidae | 55% | 100% |
A0A3Q8III2 | Leishmania donovani | 86% | 99% |
A0A422NPL9 | Trypanosoma rangeli | 32% | 100% |
A0A422P136 | Trypanosoma rangeli | 55% | 100% |
A4IC28 | Leishmania infantum | 86% | 99% |
A4Q9E8 | Mus musculus | 33% | 88% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AFW7 | Leishmania major | 85% | 100% |
E9AID0 | Leishmania braziliensis | 28% | 96% |
E9AM52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B720 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4QCW7 | Leishmania major | 27% | 100% |
Q8N841 | Homo sapiens | 31% | 85% |
V5BVF5 | Trypanosoma cruzi | 30% | 100% |