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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ADE9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005215 | transporter activity | 1 | 4 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0022804 | active transmembrane transporter activity | 3 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 4 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0140359 | ABC-type transporter activity | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 175 | 179 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.382 |
CLV_PCSK_FUR_1 | 166 | 170 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.456 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.481 |
DEG_APCC_DBOX_1 | 232 | 240 | PF00400 | 0.561 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.356 |
DOC_CYCLIN_yCln2_LP_2 | 252 | 258 | PF00134 | 0.536 |
DOC_MAPK_gen_1 | 210 | 218 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 233 | 239 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 395 | 404 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 499 | 507 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 521 | 529 | PF00069 | 0.325 |
DOC_MAPK_NFAT4_5 | 234 | 242 | PF00069 | 0.573 |
DOC_PP1_RVXF_1 | 396 | 402 | PF00149 | 0.543 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.358 |
DOC_PP1_SILK_1 | 585 | 590 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.604 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.632 |
DOC_SPAK_OSR1_1 | 197 | 201 | PF12202 | 0.554 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.746 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 601 | 606 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 620 | 630 | PF00244 | 0.362 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 601 | 605 | PF00533 | 0.258 |
LIG_CaM_IQ_9 | 261 | 277 | PF13499 | 0.541 |
LIG_EH1_1 | 424 | 432 | PF00400 | 0.318 |
LIG_EH1_1 | 491 | 499 | PF00400 | 0.507 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.591 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.543 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.656 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.567 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.403 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.404 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.589 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.522 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.501 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.562 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.592 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.637 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.587 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.800 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.361 |
LIG_GBD_Chelix_1 | 426 | 434 | PF00786 | 0.338 |
LIG_HP1_1 | 247 | 251 | PF01393 | 0.572 |
LIG_IRF3_LxIS_1 | 481 | 488 | PF10401 | 0.600 |
LIG_LIR_Gen_1 | 185 | 193 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 326 | 337 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.695 |
LIG_MYND_1 | 23 | 27 | PF01753 | 0.678 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.426 |
LIG_PCNA_yPIPBox_3 | 469 | 481 | PF02747 | 0.522 |
LIG_Pex14_1 | 359 | 363 | PF04695 | 0.435 |
LIG_Pex14_1 | 421 | 425 | PF04695 | 0.279 |
LIG_Pex14_1 | 548 | 552 | PF04695 | 0.619 |
LIG_PTAP_UEV_1 | 631 | 636 | PF05743 | 0.317 |
LIG_PTB_Apo_2 | 186 | 193 | PF02174 | 0.554 |
LIG_PTB_Apo_2 | 357 | 364 | PF02174 | 0.597 |
LIG_PTB_Apo_2 | 556 | 563 | PF02174 | 0.310 |
LIG_PTB_Phospho_1 | 357 | 363 | PF10480 | 0.600 |
LIG_PTB_Phospho_1 | 556 | 562 | PF10480 | 0.310 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.327 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.283 |
LIG_SH2_PTP2 | 486 | 489 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.599 |
LIG_SH2_STAT3 | 637 | 640 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 486 | 489 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.310 |
LIG_SH3_2 | 23 | 28 | PF14604 | 0.713 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.743 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.797 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.480 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.356 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.335 |
LIG_Sin3_3 | 138 | 145 | PF02671 | 0.420 |
LIG_SUMO_SIM_anti_2 | 246 | 254 | PF11976 | 0.559 |
LIG_SUMO_SIM_anti_2 | 299 | 307 | PF11976 | 0.500 |
LIG_SUMO_SIM_anti_2 | 656 | 662 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 246 | 254 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 659 | 664 | PF11976 | 0.331 |
LIG_SxIP_EBH_1 | 571 | 580 | PF03271 | 0.527 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.794 |
LIG_TYR_ITIM | 590 | 595 | PF00017 | 0.440 |
LIG_TYR_ITSM | 217 | 224 | PF00017 | 0.510 |
LIG_UBA3_1 | 477 | 483 | PF00899 | 0.402 |
LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.381 |
LIG_WW_1 | 393 | 396 | PF00397 | 0.558 |
LIG_WW_3 | 25 | 29 | PF00397 | 0.673 |
LIG_WW_3 | 392 | 396 | PF00397 | 0.470 |
MOD_CDC14_SPxK_1 | 230 | 233 | PF00782 | 0.264 |
MOD_CDK_SPxK_1 | 227 | 233 | PF00069 | 0.271 |
MOD_CDK_SPxxK_3 | 227 | 234 | PF00069 | 0.270 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.448 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.723 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.271 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.394 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.391 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.776 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.576 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.550 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.443 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.584 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.589 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.770 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.432 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.578 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.660 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.761 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.331 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.480 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.382 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.721 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.351 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.633 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.624 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.624 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.619 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.526 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.656 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.501 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.274 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.495 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.442 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.363 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.549 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.471 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.302 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.635 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.583 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.416 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.298 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.446 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.525 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.735 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.767 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.506 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.390 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.365 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.768 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.337 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.485 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.350 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.334 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.325 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.305 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.769 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.355 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.457 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.415 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.551 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.785 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.769 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.483 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.787 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.482 |
MOD_PKB_1 | 275 | 283 | PF00069 | 0.457 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.378 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.721 |
MOD_Plk_1 | 649 | 655 | PF00069 | 0.488 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.439 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.783 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.454 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.503 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.428 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.509 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.152 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.437 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.665 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.331 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.308 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.359 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.288 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.570 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.333 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.335 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.489 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.757 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.598 |
MOD_SUMO_for_1 | 468 | 471 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_1 | 246 | 251 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_2 | 324 | 330 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 554 | 557 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.637 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 600 | 603 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 395 | 400 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I194 | Leptomonas seymouri | 54% | 83% |
A0A0S4IZ09 | Bodo saltans | 36% | 100% |
A0A1X0P4K0 | Trypanosomatidae | 32% | 100% |
A0A3Q8IDI3 | Leishmania donovani | 91% | 100% |
A0A3R7MIF6 | Trypanosoma rangeli | 32% | 100% |
A4HFU5 | Leishmania braziliensis | 75% | 100% |
A4I2W2 | Leishmania infantum | 91% | 100% |
P45843 | Drosophila melanogaster | 24% | 100% |
Q4GZT4 | Bos taurus | 21% | 100% |
Q5MB13 | Macaca mulatta | 22% | 100% |
Q7TMS5 | Mus musculus | 21% | 100% |
Q80W57 | Rattus norvegicus | 21% | 100% |
Q8MIB3 | Sus scrofa | 22% | 100% |
Q99P81 | Mus musculus | 23% | 100% |
Q9UNQ0 | Homo sapiens | 21% | 100% |
V5B0X3 | Trypanosoma cruzi | 35% | 100% |
V5BLN9 | Trypanosoma cruzi | 24% | 99% |