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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HGW7
Term | Name | Level | Count |
---|---|---|---|
GO:0006777 | Mo-molybdopterin cofactor biosynthetic process | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0018130 | heterocycle biosynthetic process | 4 | 6 |
GO:0019637 | organophosphate metabolic process | 3 | 6 |
GO:0019720 | Mo-molybdopterin cofactor metabolic process | 4 | 6 |
GO:0032324 | molybdopterin cofactor biosynthetic process | 4 | 6 |
GO:0043545 | molybdopterin cofactor metabolic process | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0051189 | prosthetic group metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090407 | organophosphate biosynthetic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016829 | lyase activity | 2 | 1 |
GO:0016830 | carbon-carbon lyase activity | 3 | 1 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 1 |
GO:0061798 | GTP 3',8'-cyclase activity | 4 | 1 |
GO:0061799 | cyclic pyranopterin monophosphate synthase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 528 | 530 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 674 | 676 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.415 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.748 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 694 | 696 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 738 | 740 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 750 | 752 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.729 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 738 | 740 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 745 | 747 | PF00082 | 0.718 |
CLV_PCSK_PC1ET2_1 | 750 | 752 | PF00082 | 0.663 |
CLV_PCSK_PC7_1 | 741 | 747 | PF00082 | 0.690 |
CLV_PCSK_PC7_1 | 91 | 97 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 742 | 746 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.253 |
DEG_APCC_DBOX_1 | 432 | 440 | PF00400 | 0.559 |
DEG_APCC_DBOX_1 | 527 | 535 | PF00400 | 0.553 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.670 |
DEG_SCF_FBW7_1 | 7 | 13 | PF00400 | 0.708 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.562 |
DEG_SPOP_SBC_1 | 471 | 475 | PF00917 | 0.739 |
DOC_CKS1_1 | 361 | 366 | PF01111 | 0.535 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.728 |
DOC_CKS1_1 | 628 | 633 | PF01111 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.721 |
DOC_MAPK_gen_1 | 582 | 591 | PF00069 | 0.661 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.415 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.624 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 582 | 586 | PF12436 | 0.584 |
DOC_USP7_UBL2_3 | 663 | 667 | PF12436 | 0.740 |
DOC_USP7_UBL2_3 | 738 | 742 | PF12436 | 0.741 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 583 | 592 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 69 | 75 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.415 |
LIG_BIR_III_4 | 231 | 235 | PF00653 | 0.659 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.691 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 686 | 692 | PF00928 | 0.737 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.240 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.627 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.560 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.699 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.415 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.415 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.647 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.556 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.537 |
LIG_FHA_2 | 716 | 722 | PF00498 | 0.699 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 173 | 182 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.604 |
LIG_NRP_CendR_1 | 750 | 752 | PF00754 | 0.731 |
LIG_Pex14_1 | 688 | 692 | PF04695 | 0.745 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.415 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.415 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.240 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.731 |
LIG_SH3_1 | 521 | 527 | PF00018 | 0.551 |
LIG_SH3_2 | 101 | 106 | PF14604 | 0.240 |
LIG_SH3_2 | 524 | 529 | PF14604 | 0.548 |
LIG_SH3_2 | 733 | 738 | PF14604 | 0.714 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.763 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.542 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.675 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.577 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.570 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.697 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.447 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.242 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.641 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.780 |
LIG_TRAF2_1 | 482 | 485 | PF00917 | 0.617 |
LIG_TRAF2_1 | 554 | 557 | PF00917 | 0.650 |
LIG_TRAF2_1 | 711 | 714 | PF00917 | 0.656 |
LIG_WW_3 | 734 | 738 | PF00397 | 0.693 |
LIG_WW_3 | 81 | 85 | PF00397 | 0.415 |
MOD_CDC14_SPxK_1 | 430 | 433 | PF00782 | 0.604 |
MOD_CDC14_SPxK_1 | 734 | 737 | PF00782 | 0.548 |
MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.613 |
MOD_CDK_SPxK_1 | 731 | 737 | PF00069 | 0.548 |
MOD_CDK_SPxxK_3 | 514 | 521 | PF00069 | 0.572 |
MOD_CDK_SPxxK_3 | 627 | 634 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 731 | 738 | PF00069 | 0.548 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.725 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.533 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.659 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.789 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.579 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.685 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.415 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.640 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.648 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.551 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.561 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.700 |
MOD_Cter_Amidation | 519 | 522 | PF01082 | 0.745 |
MOD_Cter_Amidation | 580 | 583 | PF01082 | 0.729 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.731 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.697 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.726 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.709 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.647 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.712 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.798 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.649 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.675 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.736 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.579 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.661 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.688 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.619 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.676 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.709 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.547 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.821 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.623 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.717 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.746 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.572 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.653 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.631 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.579 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.704 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.841 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.809 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.605 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.611 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.710 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.555 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.725 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.729 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.555 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.561 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.415 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.415 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.559 |
MOD_NEK2_2 | 70 | 75 | PF00069 | 0.415 |
MOD_PK_1 | 496 | 502 | PF00069 | 0.558 |
MOD_PKA_1 | 242 | 248 | PF00069 | 0.565 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.723 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.415 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.610 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.723 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.727 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.415 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.669 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.415 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.415 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.567 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.726 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.567 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.544 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.415 |
MOD_Plk_2-3 | 256 | 262 | PF00069 | 0.592 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.421 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.490 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.640 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.633 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.687 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.625 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.415 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.801 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.568 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.765 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.740 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.544 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.618 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.594 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.434 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.561 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.605 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.286 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.827 |
TRG_ER_diArg_1 | 527 | 529 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 694 | 697 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 736 | 739 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 94 | 97 | PF00400 | 0.415 |
TRG_NES_CRM1_1 | 130 | 144 | PF08389 | 0.415 |
TRG_NLS_Bipartite_1 | 601 | 615 | PF00514 | 0.733 |
TRG_NLS_MonoCore_2 | 494 | 499 | PF00514 | 0.723 |
TRG_NLS_MonoExtC_3 | 736 | 741 | PF00514 | 0.737 |
TRG_NLS_MonoExtN_4 | 494 | 500 | PF00514 | 0.716 |
TRG_NLS_MonoExtN_4 | 610 | 615 | PF00514 | 0.727 |
TRG_NLS_MonoExtN_4 | 735 | 742 | PF00514 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.694 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 529 | 533 | PF00026 | 0.718 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDC7 | Leishmania donovani | 69% | 99% |
A4I3Z7 | Leishmania infantum | 69% | 84% |
E9B087 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 99% |
Q4Q7Z8 | Leishmania major | 67% | 100% |