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 |
Related structures:
AlphaFold database: A4HKV0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 769 | 773 | PF00656 | 0.727 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.537 |
CLV_PCSK_FUR_1 | 810 | 814 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 810 | 812 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.230 |
CLV_PCSK_PC1ET2_1 | 338 | 340 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 812 | 816 | PF00082 | 0.563 |
DEG_APCC_DBOX_1 | 448 | 456 | PF00400 | 0.383 |
DEG_APCC_DBOX_1 | 609 | 617 | PF00400 | 0.469 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.793 |
DEG_ODPH_VHL_1 | 540 | 553 | PF01847 | 0.419 |
DEG_SCF_FBW7_1 | 232 | 238 | PF00400 | 0.534 |
DEG_SPOP_SBC_1 | 236 | 240 | PF00917 | 0.767 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.768 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.343 |
DOC_CKS1_1 | 232 | 237 | PF01111 | 0.534 |
DOC_CKS1_1 | 415 | 420 | PF01111 | 0.496 |
DOC_CKS1_1 | 531 | 536 | PF01111 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 415 | 421 | PF00134 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 486 | 492 | PF00134 | 0.387 |
DOC_MAPK_DCC_7 | 46 | 56 | PF00069 | 0.655 |
DOC_MAPK_gen_1 | 538 | 545 | PF00069 | 0.400 |
DOC_MAPK_gen_1 | 547 | 555 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 569 | 579 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 608 | 615 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 547 | 555 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 452 | 458 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.619 |
DOC_PP1_RVXF_1 | 550 | 556 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 715 | 718 | PF13499 | 0.623 |
DOC_PP2B_LxvP_1 | 748 | 751 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.406 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 766 | 770 | PF00917 | 0.647 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 817 | 822 | PF00397 | 0.728 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 63 | 69 | PF00244 | 0.230 |
LIG_14-3-3_CanoR_1 | 667 | 671 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 719 | 725 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 97 | 104 | PF00244 | 0.426 |
LIG_APCC_ABBA_1 | 622 | 627 | PF00400 | 0.376 |
LIG_APCC_ABBAyCdc20_2 | 621 | 627 | PF00400 | 0.376 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.577 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 560 | 566 | PF00928 | 0.394 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.301 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.365 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.570 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.417 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.300 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.343 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.568 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.343 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.343 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.537 |
LIG_FHA_2 | 779 | 785 | PF00498 | 0.576 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.225 |
LIG_LIR_Apic_2 | 521 | 526 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 140 | 150 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 351 | 359 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 376 | 383 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 410 | 419 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 495 | 505 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 554 | 562 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 495 | 500 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 554 | 558 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.361 |
LIG_MYND_1 | 526 | 530 | PF01753 | 0.410 |
LIG_NRBOX | 654 | 660 | PF00104 | 0.488 |
LIG_PCNA_yPIPBox_3 | 2 | 15 | PF02747 | 0.523 |
LIG_PCNA_yPIPBox_3 | 565 | 574 | PF02747 | 0.436 |
LIG_Pex14_1 | 377 | 381 | PF04695 | 0.361 |
LIG_Pex14_2 | 142 | 146 | PF04695 | 0.343 |
LIG_Pex14_2 | 562 | 566 | PF04695 | 0.247 |
LIG_REV1ctd_RIR_1 | 86 | 93 | PF16727 | 0.401 |
LIG_SH2_CRK | 662 | 666 | PF00017 | 0.391 |
LIG_SH2_CRK | 752 | 756 | PF00017 | 0.564 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.523 |
LIG_SH2_SRC | 580 | 583 | PF00017 | 0.596 |
LIG_SH2_SRC | 71 | 74 | PF00017 | 0.399 |
LIG_SH2_SRC | 785 | 788 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.443 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 747 | 750 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.505 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.641 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.481 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.505 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.524 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 389 | 396 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 488 | 493 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 721 | 727 | PF11976 | 0.568 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.368 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.277 |
LIG_TRAF2_1 | 602 | 605 | PF00917 | 0.509 |
LIG_TRFH_1 | 555 | 559 | PF08558 | 0.365 |
LIG_TYR_ITIM | 69 | 74 | PF00017 | 0.399 |
LIG_UBA3_1 | 141 | 147 | PF00899 | 0.328 |
LIG_UBA3_1 | 300 | 309 | PF00899 | 0.476 |
LIG_UBA3_1 | 330 | 338 | PF00899 | 0.455 |
MOD_CDC14_SPxK_1 | 249 | 252 | PF00782 | 0.498 |
MOD_CDC14_SPxK_1 | 756 | 759 | PF00782 | 0.660 |
MOD_CDK_SPK_2 | 637 | 642 | PF00069 | 0.514 |
MOD_CDK_SPxK_1 | 246 | 252 | PF00069 | 0.514 |
MOD_CDK_SPxK_1 | 753 | 759 | PF00069 | 0.617 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.372 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.591 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.758 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.765 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.761 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.432 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.498 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.429 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.543 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.525 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.357 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.419 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.485 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.302 |
MOD_CK2_1 | 778 | 784 | PF00069 | 0.591 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.279 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.365 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.313 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.549 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.406 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.363 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.256 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.521 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.568 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.671 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.343 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.730 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.560 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.674 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.670 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.663 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.687 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.547 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.510 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.489 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.523 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.741 |
MOD_LATS_1 | 62 | 68 | PF00433 | 0.230 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.575 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.343 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.343 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.795 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.386 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.709 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.389 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.596 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.308 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.471 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.365 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.526 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.343 |
MOD_OFUCOSY | 735 | 741 | PF10250 | 0.520 |
MOD_PIKK_1 | 514 | 520 | PF00454 | 0.585 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.349 |
MOD_PIKK_1 | 672 | 678 | PF00454 | 0.324 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.564 |
MOD_PK_1 | 759 | 765 | PF00069 | 0.772 |
MOD_PKA_1 | 64 | 70 | PF00069 | 0.230 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.485 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.485 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.567 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.503 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.491 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.399 |
MOD_PKB_1 | 53 | 61 | PF00069 | 0.366 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.480 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.343 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.492 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.322 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.344 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.492 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.500 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.487 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.489 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.485 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.485 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.491 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.672 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.650 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.487 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.405 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.511 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.579 |
MOD_ProDKin_1 | 817 | 823 | PF00069 | 0.731 |
MOD_SUMO_rev_2 | 158 | 168 | PF00179 | 0.230 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.230 |
TRG_DiLeu_BaEn_1 | 389 | 394 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_1 | 482 | 487 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_1 | 496 | 501 | PF01217 | 0.538 |
TRG_DiLeu_BaEn_1 | 727 | 732 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_2 | 137 | 143 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 662 | 665 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 747 | 750 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 549 | 552 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 597 | 600 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 810 | 813 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 295 | 310 | PF08389 | 0.277 |
TRG_NLS_MonoExtC_3 | 337 | 342 | PF00514 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 170 | 174 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 290 | 295 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.278 |
TRG_Pf-PMV_PEXEL_1 | 813 | 817 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9V2 | Leptomonas seymouri | 77% | 82% |
A0A1X0NT83 | Trypanosomatidae | 51% | 82% |
A0A3S5H7S9 | Leishmania donovani | 89% | 100% |
A0A422NYM8 | Trypanosoma rangeli | 48% | 84% |
A4I8C9 | Leishmania infantum | 89% | 100% |
E9B388 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q4W7 | Leishmania major | 89% | 100% |
V5DM76 | Trypanosoma cruzi | 48% | 93% |