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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4Q3H4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016462 | pyrophosphatase activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 7 |
GO:0016887 | ATP hydrolysis activity | 7 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 606 | 610 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 636 | 640 | PF00656 | 0.713 |
CLV_C14_Caspase3-7 | 641 | 645 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 793 | 797 | PF00656 | 0.631 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.376 |
CLV_PCSK_FUR_1 | 189 | 193 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.366 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.619 |
DEG_APCC_DBOX_1 | 508 | 516 | PF00400 | 0.469 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.493 |
DOC_ANK_TNKS_1 | 474 | 481 | PF00023 | 0.573 |
DOC_CDC14_PxL_1 | 348 | 356 | PF14671 | 0.660 |
DOC_MAPK_gen_1 | 342 | 350 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 447 | 456 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 506 | 515 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 544 | 553 | PF00069 | 0.649 |
DOC_MAPK_MEF2A_6 | 509 | 517 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 482 | 488 | PF00149 | 0.515 |
DOC_PP2B_LxvP_1 | 678 | 681 | PF13499 | 0.586 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.717 |
DOC_PP4_FxxP_1 | 476 | 479 | PF00568 | 0.595 |
DOC_SPAK_OSR1_1 | 475 | 479 | PF12202 | 0.565 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 616 | 620 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.600 |
DOC_USP7_UBL2_3 | 409 | 413 | PF12436 | 0.642 |
DOC_WD40_RPTOR_TOS_1 | 533 | 539 | PF00400 | 0.611 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.737 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 131 | 141 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 447 | 452 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 484 | 488 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 788 | 793 | PF00244 | 0.610 |
LIG_Actin_WH2_2 | 522 | 540 | PF00022 | 0.592 |
LIG_AP2alpha_1 | 671 | 675 | PF02296 | 0.527 |
LIG_APCC_ABBA_1 | 372 | 377 | PF00400 | 0.643 |
LIG_APCC_ABBA_1 | 559 | 564 | PF00400 | 0.512 |
LIG_APCC_ABBAyCdc20_2 | 110 | 116 | PF00400 | 0.654 |
LIG_BIR_III_4 | 566 | 570 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.642 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.633 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.588 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.761 |
LIG_BRCT_BRCA1_1 | 402 | 406 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_2 | 104 | 110 | PF00533 | 0.621 |
LIG_CaM_IQ_9 | 575 | 591 | PF13499 | 0.609 |
LIG_CAP-Gly_1 | 793 | 801 | PF01302 | 0.655 |
LIG_CtBP_PxDLS_1 | 658 | 662 | PF00389 | 0.609 |
LIG_deltaCOP1_diTrp_1 | 115 | 125 | PF00928 | 0.678 |
LIG_eIF4E_1 | 102 | 108 | PF01652 | 0.659 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.530 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.563 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.427 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.672 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.518 |
LIG_FHA_1 | 784 | 790 | PF00498 | 0.531 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.707 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.469 |
LIG_FXI_DFP_1 | 562 | 566 | PF00024 | 0.316 |
LIG_GBD_Chelix_1 | 504 | 512 | PF00786 | 0.269 |
LIG_HCF-1_HBM_1 | 725 | 728 | PF13415 | 0.584 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.822 |
LIG_LIR_Apic_2 | 288 | 292 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 101 | 108 | PF02991 | 0.611 |
LIG_LIR_Gen_1 | 450 | 457 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 563 | 571 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 669 | 678 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 682 | 688 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 450 | 454 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 563 | 568 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 570 | 575 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 669 | 674 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 682 | 687 | PF02991 | 0.528 |
LIG_LYPXL_L_2 | 350 | 359 | PF13949 | 0.592 |
LIG_LYPXL_S_1 | 350 | 354 | PF13949 | 0.461 |
LIG_LYPXL_yS_3 | 351 | 354 | PF13949 | 0.662 |
LIG_MLH1_MIPbox_1 | 269 | 273 | PF16413 | 0.730 |
LIG_MLH1_MIPbox_1 | 452 | 456 | PF16413 | 0.527 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.325 |
LIG_PDZ_Class_3 | 796 | 801 | PF00595 | 0.715 |
LIG_Pex14_1 | 37 | 41 | PF04695 | 0.545 |
LIG_Pex14_1 | 44 | 48 | PF04695 | 0.534 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.630 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.615 |
LIG_Pex14_2 | 30 | 34 | PF04695 | 0.296 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.574 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.530 |
LIG_Pex14_2 | 671 | 675 | PF04695 | 0.527 |
LIG_Pex14_2 | 684 | 688 | PF04695 | 0.513 |
LIG_REV1ctd_RIR_1 | 38 | 47 | PF16727 | 0.548 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.618 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.641 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.516 |
LIG_SH2_PTP2 | 371 | 374 | PF00017 | 0.613 |
LIG_SH2_SRC | 102 | 105 | PF00017 | 0.605 |
LIG_SH2_SRC | 371 | 374 | PF00017 | 0.598 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 728 | 732 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.592 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.431 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.584 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.827 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.710 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.660 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 281 | 288 | PF11976 | 0.702 |
LIG_SUMO_SIM_par_1 | 281 | 288 | PF11976 | 0.702 |
LIG_SUMO_SIM_par_1 | 511 | 516 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 518 | 525 | PF11976 | 0.469 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.654 |
LIG_TYR_ITIM | 349 | 354 | PF00017 | 0.662 |
LIG_UBA3_1 | 355 | 361 | PF00899 | 0.593 |
MOD_CDK_SPK_2 | 119 | 124 | PF00069 | 0.585 |
MOD_CDK_SPxxK_3 | 119 | 126 | PF00069 | 0.583 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.723 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.728 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.696 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.719 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.660 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.684 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.670 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.655 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.411 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.768 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.787 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.626 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.708 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.469 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.633 |
MOD_CK2_1 | 745 | 751 | PF00069 | 0.495 |
MOD_Cter_Amidation | 189 | 192 | PF01082 | 0.537 |
MOD_Cter_Amidation | 740 | 743 | PF01082 | 0.387 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.472 |
MOD_GlcNHglycan | 377 | 381 | PF01048 | 0.418 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.433 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.411 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.511 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.623 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.625 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.312 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.611 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.702 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.697 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.725 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.675 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.692 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.602 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.477 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.469 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.516 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.613 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.712 |
MOD_GSK3_1 | 761 | 768 | PF00069 | 0.572 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.601 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.480 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.459 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.636 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.672 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.620 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.655 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.733 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.548 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.603 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.527 |
MOD_NEK2_2 | 404 | 409 | PF00069 | 0.642 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.555 |
MOD_NEK2_2 | 555 | 560 | PF00069 | 0.527 |
MOD_PIKK_1 | 177 | 183 | PF00454 | 0.723 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.829 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.645 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.570 |
MOD_PIKK_1 | 610 | 616 | PF00454 | 0.734 |
MOD_PIKK_1 | 718 | 724 | PF00454 | 0.571 |
MOD_PIKK_1 | 745 | 751 | PF00454 | 0.525 |
MOD_PK_1 | 743 | 749 | PF00069 | 0.601 |
MOD_PK_1 | 788 | 794 | PF00069 | 0.618 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.723 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.553 |
MOD_PKA_2 | 602 | 608 | PF00069 | 0.815 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.673 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.598 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.706 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.624 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.674 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.539 |
MOD_Plk_1 | 733 | 739 | PF00069 | 0.698 |
MOD_Plk_2-3 | 519 | 525 | PF00069 | 0.455 |
MOD_Plk_2-3 | 635 | 641 | PF00069 | 0.692 |
MOD_Plk_2-3 | 664 | 670 | PF00069 | 0.599 |
MOD_Plk_2-3 | 733 | 739 | PF00069 | 0.569 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.598 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.692 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.698 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.612 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.654 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.623 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.528 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.525 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.584 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.476 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.525 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.673 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.533 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.618 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.263 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.583 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.394 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.619 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.735 |
MOD_SUMO_rev_2 | 269 | 279 | PF00179 | 0.701 |
TRG_DiLeu_BaEn_2 | 151 | 157 | PF01217 | 0.628 |
TRG_DiLeu_BaLyEn_6 | 695 | 700 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.662 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.594 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.645 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 291 | 296 | PF00026 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDZ4 | Leptomonas seymouri | 50% | 97% |
A0A3Q8IUC9 | Leishmania donovani | 91% | 100% |
A4HAE8 | Leishmania braziliensis | 67% | 100% |
A4I9K4 | Leishmania infantum | 91% | 100% |
E9B4K2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |