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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005657 | replication fork | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0035861 | site of double-strand break | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0090734 | site of DNA damage | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBQ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0042276 | error-prone translesion synthesis | 8 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0003684 | damaged DNA binding | 5 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0034061 | DNA polymerase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 526 | 530 | PF00656 | 0.702 |
CLV_MEL_PAP_1 | 426 | 432 | PF00089 | 0.371 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.718 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 620 | 622 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 620 | 622 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 693 | 695 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.778 |
CLV_Separin_Metazoa | 189 | 193 | PF03568 | 0.548 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.621 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.579 |
DEG_COP1_1 | 521 | 530 | PF00400 | 0.576 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.323 |
DOC_CKS1_1 | 451 | 456 | PF01111 | 0.521 |
DOC_CYCLIN_RxL_1 | 218 | 229 | PF00134 | 0.548 |
DOC_CYCLIN_RxL_1 | 545 | 553 | PF00134 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 681 | 687 | PF00134 | 0.572 |
DOC_MAPK_DCC_7 | 61 | 69 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 439 | 448 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 633 | 643 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 439 | 448 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 636 | 643 | PF00069 | 0.637 |
DOC_MAPK_RevD_3 | 153 | 169 | PF00069 | 0.541 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.474 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.548 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.758 |
DOC_USP7_UBL2_3 | 693 | 697 | PF12436 | 0.781 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 429 | 437 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 702 | 706 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 723 | 729 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 89 | 97 | PF00244 | 0.510 |
LIG_AP2alpha_2 | 698 | 700 | PF02296 | 0.579 |
LIG_APCC_ABBAyCdc20_2 | 236 | 242 | PF00400 | 0.548 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 401 | 405 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 671 | 675 | PF00533 | 0.702 |
LIG_deltaCOP1_diTrp_1 | 425 | 430 | PF00928 | 0.379 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.548 |
LIG_EVH1_2 | 545 | 549 | PF00568 | 0.344 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.524 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.475 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.592 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.578 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.575 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.575 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.708 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.474 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.575 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.664 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.615 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.608 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.455 |
LIG_FHA_2 | 693 | 699 | PF00498 | 0.731 |
LIG_LIR_Apic_2 | 280 | 286 | PF02991 | 0.465 |
LIG_LIR_Apic_2 | 313 | 318 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 450 | 454 | PF02991 | 0.428 |
LIG_LIR_Apic_2 | 79 | 85 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 10 | 21 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 425 | 433 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 489 | 497 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 590 | 599 | PF02991 | 0.651 |
LIG_LIR_LC3C_4 | 443 | 446 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.643 |
LIG_REV1ctd_RIR_1 | 673 | 682 | PF16727 | 0.546 |
LIG_SH2_GRB2like | 349 | 352 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.548 |
LIG_SH2_PTP2 | 128 | 131 | PF00017 | 0.548 |
LIG_SH2_PTP2 | 451 | 454 | PF00017 | 0.514 |
LIG_SH2_SRC | 128 | 131 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 433 | 437 | PF00017 | 0.594 |
LIG_SH2_STAT3 | 466 | 469 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.579 |
LIG_SH3_1 | 558 | 564 | PF00018 | 0.492 |
LIG_SH3_1 | 82 | 88 | PF00018 | 0.537 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.548 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.548 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.544 |
LIG_SH3_3 | 525 | 531 | PF00018 | 0.789 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.729 |
LIG_SH3_3 | 734 | 740 | PF00018 | 0.703 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.537 |
LIG_SH3_4 | 266 | 273 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.517 |
LIG_SUMO_SIM_anti_2 | 551 | 556 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 638 | 645 | PF11976 | 0.681 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.433 |
LIG_TRFH_1 | 53 | 57 | PF08558 | 0.457 |
MOD_CDK_SPxxK_3 | 686 | 693 | PF00069 | 0.608 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.551 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.593 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.729 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.704 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.590 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.644 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.398 |
MOD_CK2_1 | 707 | 713 | PF00069 | 0.812 |
MOD_CK2_1 | 743 | 749 | PF00069 | 0.697 |
MOD_GlcNHglycan | 246 | 250 | PF01048 | 0.414 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.488 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.455 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.496 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.419 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.458 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.579 |
MOD_GlcNHglycan | 540 | 544 | PF01048 | 0.664 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.716 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.615 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.704 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.637 |
MOD_GlcNHglycan | 708 | 712 | PF01048 | 0.738 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.745 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.662 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.590 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.698 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.740 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.784 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.593 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.457 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.782 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.739 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.414 |
MOD_N-GLC_1 | 597 | 602 | PF02516 | 0.540 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.516 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.408 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.426 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.386 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.761 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.547 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.542 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.759 |
MOD_PKA_1 | 353 | 359 | PF00069 | 0.642 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.414 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.633 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.418 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.557 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.711 |
MOD_PKB_1 | 619 | 627 | PF00069 | 0.724 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.368 |
MOD_Plk_1 | 539 | 545 | PF00069 | 0.517 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.433 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.546 |
MOD_Plk_1 | 733 | 739 | PF00069 | 0.509 |
MOD_Plk_2-3 | 648 | 654 | PF00069 | 0.697 |
MOD_Plk_2-3 | 749 | 755 | PF00069 | 0.668 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.476 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.329 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.558 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.473 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.551 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.414 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.525 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.687 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.402 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.758 |
MOD_SUMO_rev_2 | 366 | 372 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 500 | 508 | PF00179 | 0.518 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 440 | 445 | PF01217 | 0.538 |
TRG_DiLeu_BaEn_1 | 489 | 494 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 160 | 165 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 557 | 560 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.724 |
TRG_NLS_MonoExtC_3 | 618 | 623 | PF00514 | 0.712 |
TRG_NLS_MonoExtN_4 | 619 | 624 | PF00514 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 633 | 637 | PF00026 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 694 | 698 | PF00026 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU7 | Leptomonas seymouri | 52% | 95% |
A0A3S5H795 | Leishmania donovani | 74% | 99% |
A4HZ61 | Leishmania infantum | 80% | 96% |
E8NHQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
E9AV29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 98% |
Q4QCF3 | Leishmania major | 79% | 100% |