Protein modification, Uncharacterized
| 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: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: A4I479
| 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 | 3 |
| 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:0016874 | ligase activity | 2 | 3 |
| GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 1 |
| GO:0016881 | acid-amino acid ligase activity | 4 | 1 |
| 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 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.252 |
| CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.252 |
| CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.302 |
| CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.338 |
| CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.266 |
| CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.651 |
| CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.384 |
| CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.437 |
| CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.492 |
| CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.538 |
| CLV_PCSK_FUR_1 | 165 | 169 | PF00082 | 0.297 |
| CLV_PCSK_FUR_1 | 433 | 437 | PF00082 | 0.440 |
| CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.264 |
| CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.264 |
| CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.701 |
| CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.302 |
| CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.343 |
| CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.329 |
| CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.650 |
| CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.404 |
| CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.437 |
| CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.492 |
| CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.538 |
| CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.340 |
| CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.701 |
| CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.338 |
| CLV_PCSK_PC7_1 | 256 | 262 | PF00082 | 0.338 |
| CLV_PCSK_PC7_1 | 294 | 300 | PF00082 | 0.587 |
| CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.594 |
| CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.254 |
| CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.334 |
| CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.338 |
| CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.333 |
| CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.463 |
| CLV_Separin_Metazoa | 451 | 455 | PF03568 | 0.511 |
| DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.559 |
| DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.518 |
| DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.467 |
| DOC_CKS1_1 | 103 | 108 | PF01111 | 0.538 |
| DOC_CYCLIN_RxL_1 | 184 | 192 | PF00134 | 0.502 |
| DOC_CYCLIN_yCln2_LP_2 | 191 | 197 | PF00134 | 0.557 |
| DOC_CYCLIN_yCln2_LP_2 | 378 | 384 | PF00134 | 0.407 |
| DOC_MAPK_DCC_7 | 484 | 493 | PF00069 | 0.538 |
| DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.559 |
| DOC_MAPK_gen_1 | 256 | 267 | PF00069 | 0.519 |
| DOC_MAPK_gen_1 | 278 | 286 | PF00069 | 0.463 |
| DOC_MAPK_MEF2A_6 | 260 | 269 | PF00069 | 0.485 |
| DOC_MAPK_MEF2A_6 | 278 | 286 | PF00069 | 0.355 |
| DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.452 |
| DOC_MAPK_NFAT4_5 | 279 | 287 | PF00069 | 0.557 |
| DOC_PP1_RVXF_1 | 143 | 150 | PF00149 | 0.464 |
| DOC_PP1_RVXF_1 | 222 | 229 | PF00149 | 0.557 |
| DOC_PP1_RVXF_1 | 71 | 78 | PF00149 | 0.497 |
| DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.557 |
| DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.573 |
| DOC_PP2B_LxvP_1 | 425 | 428 | PF13499 | 0.474 |
| DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.502 |
| DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.723 |
| DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.755 |
| DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.499 |
| DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.538 |
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.519 |
| DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.585 |
| DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.499 |
| DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.466 |
| DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.765 |
| DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.641 |
| DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.452 |
| DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.557 |
| LIG_14-3-3_CanoR_1 | 157 | 166 | PF00244 | 0.420 |
| LIG_14-3-3_CanoR_1 | 242 | 247 | PF00244 | 0.538 |
| LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.766 |
| LIG_14-3-3_CanoR_1 | 374 | 379 | PF00244 | 0.524 |
| LIG_14-3-3_CanoR_1 | 433 | 439 | PF00244 | 0.430 |
| LIG_Actin_WH2_2 | 470 | 486 | PF00022 | 0.499 |
| LIG_Actin_WH2_2 | 504 | 519 | PF00022 | 0.515 |
| LIG_APCC_ABBA_1 | 265 | 270 | PF00400 | 0.538 |
| LIG_APCC_ABBA_1 | 337 | 342 | PF00400 | 0.452 |
| LIG_Clathr_ClatBox_1 | 476 | 480 | PF01394 | 0.452 |
| LIG_eIF4E_1 | 268 | 274 | PF01652 | 0.513 |
| LIG_EVH1_2 | 88 | 92 | PF00568 | 0.469 |
| LIG_FHA_1 | 373 | 379 | PF00498 | 0.550 |
| LIG_FHA_1 | 441 | 447 | PF00498 | 0.485 |
| LIG_FHA_1 | 517 | 523 | PF00498 | 0.538 |
| LIG_FHA_1 | 584 | 590 | PF00498 | 0.655 |
| LIG_FHA_2 | 232 | 238 | PF00498 | 0.538 |
| LIG_FHA_2 | 243 | 249 | PF00498 | 0.482 |
| LIG_FHA_2 | 250 | 256 | PF00498 | 0.376 |
| LIG_FHA_2 | 503 | 509 | PF00498 | 0.493 |
| LIG_FHA_2 | 561 | 567 | PF00498 | 0.573 |
| LIG_FHA_2 | 76 | 82 | PF00498 | 0.535 |
| LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.554 |
| LIG_LIR_Gen_1 | 196 | 203 | PF02991 | 0.513 |
| LIG_LIR_Gen_1 | 472 | 482 | PF02991 | 0.540 |
| LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.382 |
| LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.554 |
| LIG_LIR_Nem_3 | 196 | 200 | PF02991 | 0.513 |
| LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.538 |
| LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.457 |
| LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.394 |
| LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.410 |
| LIG_NRBOX | 283 | 289 | PF00104 | 0.557 |
| LIG_REV1ctd_RIR_1 | 225 | 231 | PF16727 | 0.493 |
| LIG_SH2_CRK | 130 | 134 | PF00017 | 0.538 |
| LIG_SH2_CRK | 352 | 356 | PF00017 | 0.452 |
| LIG_SH2_CRK | 65 | 69 | PF00017 | 0.344 |
| LIG_SH2_GRB2like | 322 | 325 | PF00017 | 0.479 |
| LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.452 |
| LIG_SH2_PTP2 | 285 | 288 | PF00017 | 0.523 |
| LIG_SH2_SRC | 379 | 382 | PF00017 | 0.563 |
| LIG_SH2_STAP1 | 540 | 544 | PF00017 | 0.559 |
| LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.455 |
| LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.452 |
| LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.500 |
| LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.563 |
| LIG_SH3_3 | 100 | 106 | PF00018 | 0.625 |
| LIG_SH3_3 | 163 | 169 | PF00018 | 0.510 |
| LIG_SH3_3 | 266 | 272 | PF00018 | 0.452 |
| LIG_SH3_3 | 37 | 43 | PF00018 | 0.553 |
| LIG_SH3_3 | 395 | 401 | PF00018 | 0.721 |
| LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.452 |
| LIG_SUMO_SIM_par_1 | 285 | 291 | PF11976 | 0.545 |
| LIG_SUMO_SIM_par_1 | 442 | 448 | PF11976 | 0.317 |
| LIG_SUMO_SIM_par_1 | 608 | 613 | PF11976 | 0.534 |
| LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.501 |
| LIG_TYR_ITSM | 61 | 68 | PF00017 | 0.399 |
| LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.474 |
| MOD_CDC14_SPxK_1 | 99 | 102 | PF00782 | 0.606 |
| MOD_CDK_SPxK_1 | 96 | 102 | PF00069 | 0.567 |
| MOD_CK1_1 | 196 | 202 | PF00069 | 0.457 |
| MOD_CK1_1 | 218 | 224 | PF00069 | 0.405 |
| MOD_CK1_1 | 297 | 303 | PF00069 | 0.729 |
| MOD_CK1_1 | 323 | 329 | PF00069 | 0.510 |
| MOD_CK1_1 | 96 | 102 | PF00069 | 0.660 |
| MOD_CK2_1 | 180 | 186 | PF00069 | 0.564 |
| MOD_CK2_1 | 231 | 237 | PF00069 | 0.560 |
| MOD_CK2_1 | 242 | 248 | PF00069 | 0.499 |
| MOD_CK2_1 | 249 | 255 | PF00069 | 0.396 |
| MOD_CK2_1 | 417 | 423 | PF00069 | 0.491 |
| MOD_CK2_1 | 434 | 440 | PF00069 | 0.421 |
| MOD_CK2_1 | 445 | 451 | PF00069 | 0.280 |
| MOD_CK2_1 | 469 | 475 | PF00069 | 0.557 |
| MOD_CK2_1 | 560 | 566 | PF00069 | 0.370 |
| MOD_CK2_1 | 79 | 85 | PF00069 | 0.514 |
| MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.313 |
| MOD_DYRK1A_RPxSP_1 | 102 | 106 | PF00069 | 0.571 |
| MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.316 |
| MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.730 |
| MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.324 |
| MOD_GlcNHglycan | 51 | 55 | PF01048 | 0.623 |
| MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.311 |
| MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.552 |
| MOD_GSK3_1 | 115 | 122 | PF00069 | 0.454 |
| MOD_GSK3_1 | 153 | 160 | PF00069 | 0.522 |
| MOD_GSK3_1 | 189 | 196 | PF00069 | 0.471 |
| MOD_GSK3_1 | 294 | 301 | PF00069 | 0.671 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.494 |
| MOD_GSK3_1 | 318 | 325 | PF00069 | 0.639 |
| MOD_GSK3_1 | 361 | 368 | PF00069 | 0.497 |
| MOD_GSK3_1 | 407 | 414 | PF00069 | 0.541 |
| MOD_GSK3_1 | 417 | 424 | PF00069 | 0.486 |
| MOD_GSK3_1 | 75 | 82 | PF00069 | 0.479 |
| MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.687 |
| MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.281 |
| MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.252 |
| MOD_NEK2_1 | 153 | 158 | PF00069 | 0.504 |
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.530 |
| MOD_NEK2_1 | 288 | 293 | PF00069 | 0.486 |
| MOD_NEK2_1 | 421 | 426 | PF00069 | 0.511 |
| MOD_NEK2_1 | 502 | 507 | PF00069 | 0.477 |
| MOD_NEK2_1 | 516 | 521 | PF00069 | 0.477 |
| MOD_NEK2_1 | 522 | 527 | PF00069 | 0.321 |
| MOD_NEK2_1 | 560 | 565 | PF00069 | 0.519 |
| MOD_PKA_1 | 298 | 304 | PF00069 | 0.766 |
| MOD_PKA_2 | 241 | 247 | PF00069 | 0.538 |
| MOD_PKA_2 | 297 | 303 | PF00069 | 0.751 |
| MOD_PKA_2 | 373 | 379 | PF00069 | 0.444 |
| MOD_PKA_2 | 434 | 440 | PF00069 | 0.420 |
| MOD_PKA_2 | 516 | 522 | PF00069 | 0.557 |
| MOD_PKA_2 | 560 | 566 | PF00069 | 0.552 |
| MOD_PKA_2 | 60 | 66 | PF00069 | 0.530 |
| MOD_Plk_1 | 115 | 121 | PF00069 | 0.394 |
| MOD_Plk_1 | 181 | 187 | PF00069 | 0.502 |
| MOD_Plk_1 | 318 | 324 | PF00069 | 0.554 |
| MOD_Plk_1 | 75 | 81 | PF00069 | 0.529 |
| MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.577 |
| MOD_Plk_4 | 115 | 121 | PF00069 | 0.394 |
| MOD_Plk_4 | 374 | 380 | PF00069 | 0.557 |
| MOD_Plk_4 | 417 | 423 | PF00069 | 0.487 |
| MOD_Plk_4 | 442 | 448 | PF00069 | 0.325 |
| MOD_Plk_4 | 497 | 503 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.517 |
| MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.499 |
| MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.466 |
| MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.765 |
| MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.635 |
| MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.567 |
| MOD_SUMO_rev_2 | 541 | 550 | PF00179 | 0.575 |
| TRG_DiLeu_BaEn_3 | 553 | 559 | PF01217 | 0.426 |
| TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.513 |
| TRG_DiLeu_BaLyEn_6 | 518 | 523 | PF01217 | 0.477 |
| TRG_DiLeu_BaLyEn_6 | 569 | 574 | PF01217 | 0.486 |
| TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.538 |
| TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.538 |
| TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.452 |
| TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.352 |
| TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.450 |
| TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.499 |
| TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.502 |
| TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.424 |
| TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.424 |
| TRG_ER_diArg_1 | 570 | 572 | PF00400 | 0.490 |
| TRG_ER_diArg_1 | 614 | 616 | PF00400 | 0.582 |
| TRG_NES_CRM1_1 | 440 | 456 | PF08389 | 0.487 |
| TRG_Pf-PMV_PEXEL_1 | 150 | 154 | PF00026 | 0.321 |
| TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.272 |
| TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.469 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IAP5 | Leptomonas seymouri | 25% | 83% |
| A0A0N1IH77 | Leptomonas seymouri | 56% | 100% |
| A0A0S4J7C9 | Bodo saltans | 25% | 93% |
| A0A0S4JH38 | Bodo saltans | 33% | 100% |
| A0A0S4KQK8 | Bodo saltans | 27% | 94% |
| A0A1X0P0Y5 | Trypanosomatidae | 37% | 100% |
| A0A1X0P6A0 | Trypanosomatidae | 26% | 93% |
| A0A3Q8IDL7 | Leishmania donovani | 23% | 100% |
| A0A3Q8III2 | Leishmania donovani | 27% | 85% |
| A0A3S7X261 | Leishmania donovani | 100% | 100% |
| A0A422N064 | Trypanosoma rangeli | 42% | 100% |
| A0A422N932 | Trypanosoma rangeli | 26% | 100% |
| A0A422P136 | Trypanosoma rangeli | 25% | 94% |
| A4HH59 | Leishmania braziliensis | 75% | 100% |
| A4HYN9 | Leishmania infantum | 23% | 100% |
| A4IC28 | Leishmania infantum | 27% | 85% |
| A4Q9E8 | Mus musculus | 26% | 75% |
| A4Q9F6 | Mus musculus | 24% | 77% |
| A6NNM8 | Homo sapiens | 25% | 76% |
| A8CVX7 | Danio rerio | 27% | 79% |
| B6DTF7 | Bodo saltans | 22% | 100% |
| C9ZI96 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 90% |
| C9ZKP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
| C9ZPR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
| C9ZYH1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 94% |
| D0A044 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
| E9ADM8 | Leishmania major | 92% | 100% |
| E9AFW7 | Leishmania major | 26% | 85% |
| E9AID0 | Leishmania braziliensis | 24% | 100% |
| E9AM52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
| E9B720 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 85% |
| Q8N841 | Homo sapiens | 25% | 73% |
| V5ARK1 | Trypanosoma cruzi | 26% | 100% |
| V5B4U2 | Trypanosoma cruzi | 42% | 100% |