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: 12 |
NetGPI | no | yes: 0, no: 12 |
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: E9B720
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
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 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0004835 | tubulin-tyrosine ligase activity | 3 | 4 |
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:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 4 |
GO:0016881 | acid-amino acid ligase activity | 4 | 4 |
GO:0070739 | protein-glutamic acid ligase activity | 3 | 1 |
GO:0070740 | tubulin-glutamic acid ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 701 | 703 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 716 | 718 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 492 | 494 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 716 | 718 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 171 | 177 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 642 | 646 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.610 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.368 |
DEG_SCF_FBW7_1 | 50 | 57 | PF00400 | 0.614 |
DOC_CKS1_1 | 353 | 358 | PF01111 | 0.530 |
DOC_CYCLIN_RxL_1 | 171 | 180 | PF00134 | 0.567 |
DOC_CYCLIN_RxL_1 | 638 | 647 | PF00134 | 0.480 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 553 | 562 | PF00134 | 0.520 |
DOC_MAPK_FxFP_2 | 193 | 196 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 409 | 415 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 559 | 567 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 559 | 567 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 86 | 95 | PF00069 | 0.589 |
DOC_PP1_RVXF_1 | 506 | 512 | PF00149 | 0.454 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.636 |
DOC_PP2B_PxIxI_1 | 358 | 364 | PF00149 | 0.473 |
DOC_PP4_FxxP_1 | 107 | 110 | PF00568 | 0.668 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.733 |
DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 336 | 339 | PF00568 | 0.460 |
DOC_PP4_FxxP_1 | 648 | 651 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 78 | 82 | PF12436 | 0.424 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.659 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 225 | 231 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 268 | 276 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 283 | 287 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 493 | 503 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 584 | 593 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 642 | 651 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 81 | 86 | PF00244 | 0.590 |
LIG_Actin_RPEL_3 | 577 | 596 | PF02755 | 0.488 |
LIG_Actin_WH2_2 | 252 | 270 | PF00022 | 0.436 |
LIG_APCC_ABBA_1 | 427 | 432 | PF00400 | 0.449 |
LIG_APCC_ABBAyCdc20_2 | 426 | 432 | PF00400 | 0.439 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.699 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.650 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.473 |
LIG_Clathr_ClatBox_1 | 547 | 551 | PF01394 | 0.530 |
LIG_deltaCOP1_diTrp_1 | 483 | 491 | PF00928 | 0.488 |
LIG_eIF4E_1 | 399 | 405 | PF01652 | 0.488 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.461 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.471 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.747 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.744 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.460 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.571 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.655 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.321 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.451 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.613 |
LIG_FHA_2 | 418 | 424 | PF00498 | 0.449 |
LIG_LIR_Apic_2 | 106 | 110 | PF02991 | 0.655 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.725 |
LIG_LIR_Apic_2 | 192 | 196 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 208 | 212 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 335 | 339 | PF02991 | 0.440 |
LIG_LIR_Apic_2 | 646 | 651 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 229 | 240 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 326 | 337 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 520 | 529 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 678 | 682 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 7 | 11 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.605 |
LIG_LYPXL_yS_3 | 90 | 93 | PF13949 | 0.598 |
LIG_MLH1_MIPbox_1 | 191 | 195 | PF16413 | 0.368 |
LIG_MYND_1 | 58 | 62 | PF01753 | 0.582 |
LIG_PCNA_yPIPBox_3 | 657 | 667 | PF02747 | 0.242 |
LIG_Pex14_2 | 228 | 232 | PF04695 | 0.250 |
LIG_Pex14_2 | 276 | 280 | PF04695 | 0.335 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.439 |
LIG_PTB_Apo_2 | 106 | 113 | PF02174 | 0.613 |
LIG_PTB_Apo_2 | 628 | 635 | PF02174 | 0.502 |
LIG_PTB_Phospho_1 | 106 | 112 | PF10480 | 0.607 |
LIG_RPA_C_Fungi | 117 | 129 | PF08784 | 0.729 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.320 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.308 |
LIG_SH2_SRC | 112 | 115 | PF00017 | 0.715 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.188 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.144 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.547 |
LIG_SH3_1 | 379 | 385 | PF00018 | 0.338 |
LIG_SH3_2 | 353 | 358 | PF14604 | 0.418 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.429 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.406 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.320 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.477 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.533 |
LIG_SUMO_SIM_par_1 | 662 | 668 | PF11976 | 0.338 |
LIG_SxIP_EBH_1 | 24 | 34 | PF03271 | 0.452 |
LIG_TRAF2_2 | 445 | 450 | PF00917 | 0.418 |
LIG_UBA3_1 | 360 | 365 | PF00899 | 0.338 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.338 |
LIG_WRC_WIRS_1 | 518 | 523 | PF05994 | 0.418 |
LIG_WRC_WIRS_1 | 645 | 650 | PF05994 | 0.439 |
MOD_CDK_SPxK_1 | 352 | 358 | PF00069 | 0.418 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.696 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.442 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.657 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.370 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.517 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.661 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.387 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.523 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.293 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.407 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.536 |
MOD_CK2_1 | 656 | 662 | PF00069 | 0.401 |
MOD_Cter_Amidation | 307 | 310 | PF01082 | 0.291 |
MOD_Cter_Amidation | 407 | 410 | PF01082 | 0.320 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.705 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.565 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.406 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.454 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.697 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.399 |
MOD_GlcNHglycan | 538 | 542 | PF01048 | 0.362 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.588 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.402 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.686 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.590 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.631 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.600 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.457 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.317 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.645 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.414 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.501 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.488 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.508 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.291 |
MOD_N-GLC_1 | 606 | 611 | PF02516 | 0.605 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.263 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.699 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.594 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.457 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.500 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.372 |
MOD_NEK2_2 | 675 | 680 | PF00069 | 0.199 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.559 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.634 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.471 |
MOD_PKA_1 | 440 | 446 | PF00069 | 0.362 |
MOD_PKA_1 | 599 | 605 | PF00069 | 0.549 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.599 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.677 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.468 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.487 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.488 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.309 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.545 |
MOD_PKA_2 | 700 | 706 | PF00069 | 0.423 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.620 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.729 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.495 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.291 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.541 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.528 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.338 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.377 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.482 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.488 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.304 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.348 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.486 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.315 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.404 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.655 |
TRG_DiLeu_BaEn_4 | 165 | 171 | PF01217 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 400 | 405 | PF01217 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 558 | 563 | PF01217 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 640 | 645 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.598 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 598 | 600 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 700 | 702 | PF00400 | 0.428 |
TRG_NLS_MonoExtN_4 | 78 | 85 | PF00514 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAP5 | Leptomonas seymouri | 76% | 98% |
A0A0S4J7C9 | Bodo saltans | 50% | 100% |
A0A0S4KQK8 | Bodo saltans | 34% | 100% |
A0A1X0NXX8 | Trypanosomatidae | 30% | 100% |
A0A1X0P6A0 | Trypanosomatidae | 56% | 100% |
A0A3Q8III2 | Leishmania donovani | 96% | 100% |
A0A3S7X261 | Leishmania donovani | 27% | 100% |
A0A422NPL9 | Trypanosoma rangeli | 32% | 100% |
A0A422P136 | Trypanosoma rangeli | 54% | 100% |
A4HNF6 | Leishmania braziliensis | 87% | 99% |
A4I479 | Leishmania infantum | 27% | 100% |
A4IC28 | Leishmania infantum | 96% | 100% |
A4Q9E8 | Mus musculus | 32% | 88% |
C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ADM8 | Leishmania major | 27% | 100% |
E9AFW7 | Leishmania major | 94% | 100% |
E9AID0 | Leishmania braziliensis | 28% | 97% |
E9AM52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4QCW7 | Leishmania major | 26% | 100% |