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 |
Related structures:
AlphaFold database: Q4QG05
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0031848 | protection from non-homologous end joining at telomere | 6 | 2 |
GO:0032200 | telomere organization | 6 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0036297 | interstrand cross-link repair | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043247 | telomere maintenance in response to DNA damage | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003684 | damaged DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004518 | nuclease activity | 4 | 2 |
GO:0004527 | exonuclease activity | 5 | 2 |
GO:0004529 | DNA exonuclease activity | 5 | 2 |
GO:0004536 | DNA nuclease activity | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0035312 | 5'-3' DNA exonuclease activity | 7 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.487 |
CLV_C14_Caspase3-7 | 768 | 772 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.671 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.721 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 705 | 707 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.693 |
CLV_Separin_Metazoa | 412 | 416 | PF03568 | 0.404 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.445 |
DEG_SCF_FBW7_1 | 251 | 256 | PF00400 | 0.649 |
DEG_SPOP_SBC_1 | 253 | 257 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 643 | 647 | PF00917 | 0.694 |
DOC_ANK_TNKS_1 | 671 | 678 | PF00023 | 0.645 |
DOC_CKS1_1 | 126 | 131 | PF01111 | 0.453 |
DOC_CYCLIN_RxL_1 | 58 | 69 | PF00134 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 112 | 118 | PF00134 | 0.350 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.385 |
DOC_MAPK_DCC_7 | 403 | 413 | PF00069 | 0.645 |
DOC_MAPK_gen_1 | 598 | 606 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 672 | 680 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 705 | 711 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 72 | 80 | PF00069 | 0.376 |
DOC_MAPK_HePTP_8 | 500 | 512 | PF00069 | 0.556 |
DOC_MAPK_JIP1_4 | 600 | 606 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 268 | 277 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.639 |
DOC_MAPK_MEF2A_6 | 503 | 512 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 705 | 713 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 72 | 80 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 748 | 755 | PF00069 | 0.620 |
DOC_PP2B_LxvP_1 | 508 | 511 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 604 | 607 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.479 |
DOC_PP2B_PxIxI_1 | 408 | 414 | PF00149 | 0.531 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.358 |
DOC_PP4_FxxP_1 | 638 | 641 | PF00568 | 0.731 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.331 |
LIG_14-3-3_CanoR_1 | 307 | 312 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 447 | 455 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 483 | 488 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 679 | 684 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 725 | 733 | PF00244 | 0.721 |
LIG_Actin_WH2_2 | 666 | 681 | PF00022 | 0.553 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 635 | 639 | PF00533 | 0.633 |
LIG_eIF4E_1 | 545 | 551 | PF01652 | 0.469 |
LIG_EVH1_2 | 593 | 597 | PF00568 | 0.545 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.497 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.447 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.593 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.319 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.658 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.703 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.713 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.394 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.448 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.489 |
LIG_FHA_2 | 729 | 735 | PF00498 | 0.562 |
LIG_HCF-1_HBM_1 | 162 | 165 | PF13415 | 0.357 |
LIG_KLC1_Yacidic_2 | 162 | 167 | PF13176 | 0.356 |
LIG_LIR_Apic_2 | 636 | 641 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 477 | 485 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 11 | 16 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 180 | 184 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 443 | 448 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 477 | 481 | PF02991 | 0.434 |
LIG_LYPXL_SIV_4 | 544 | 552 | PF13949 | 0.347 |
LIG_MLH1_MIPbox_1 | 635 | 639 | PF16413 | 0.633 |
LIG_NRBOX | 204 | 210 | PF00104 | 0.576 |
LIG_PCNA_PIPBox_1 | 149 | 158 | PF02747 | 0.436 |
LIG_PDZ_Class_2 | 770 | 775 | PF00595 | 0.699 |
LIG_Pex14_2 | 33 | 37 | PF04695 | 0.471 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.469 |
LIG_SH2_CRK | 438 | 442 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.359 |
LIG_SH2_SRC | 545 | 548 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.469 |
LIG_SH2_STAT3 | 227 | 230 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.732 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.644 |
LIG_SH3_1 | 541 | 547 | PF00018 | 0.518 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.425 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.684 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.567 |
LIG_Sin3_3 | 548 | 555 | PF02671 | 0.383 |
LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 307 | 313 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 483 | 488 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 5 | 12 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 760 | 768 | PF11976 | 0.618 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.479 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.499 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.487 |
LIG_TRAF2_1 | 588 | 591 | PF00917 | 0.733 |
LIG_TYR_ITSM | 433 | 440 | PF00017 | 0.581 |
LIG_WRC_WIRS_1 | 152 | 157 | PF05994 | 0.465 |
LIG_WW_3 | 592 | 596 | PF00397 | 0.541 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.440 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.328 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.638 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.715 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.469 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.703 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.801 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.577 |
MOD_CK1_1 | 757 | 763 | PF00069 | 0.665 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.552 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.452 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.527 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.480 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.458 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.590 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.666 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.560 |
MOD_CMANNOS | 379 | 382 | PF00535 | 0.487 |
MOD_Cter_Amidation | 221 | 224 | PF01082 | 0.482 |
MOD_Cter_Amidation | 703 | 706 | PF01082 | 0.760 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.410 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.496 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.629 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.620 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.742 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.579 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.595 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.468 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.623 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.413 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.592 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.258 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.736 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.668 |
MOD_GlcNHglycan | 656 | 660 | PF01048 | 0.827 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.738 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.790 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.693 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.519 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.444 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.545 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.653 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.448 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.511 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.729 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.615 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.286 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.747 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.413 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.460 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.693 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.413 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.621 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.662 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.690 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.574 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.755 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.656 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.611 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.600 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.671 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.420 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.592 |
MOD_LATS_1 | 41 | 47 | PF00433 | 0.514 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.754 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.461 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.520 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.226 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.414 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.389 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.443 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.505 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.699 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.559 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.700 |
MOD_NEK2_2 | 398 | 403 | PF00069 | 0.663 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.602 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.557 |
MOD_PIKK_1 | 447 | 453 | PF00454 | 0.671 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.589 |
MOD_PIKK_1 | 690 | 696 | PF00454 | 0.694 |
MOD_PK_1 | 483 | 489 | PF00069 | 0.361 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.491 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.651 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.542 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.667 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.559 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.394 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.725 |
MOD_Plk_1 | 665 | 671 | PF00069 | 0.663 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.383 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.411 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.384 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.525 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.634 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.763 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.723 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.530 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.565 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.446 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.726 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.693 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.694 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.594 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.429 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.409 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.652 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.329 |
MOD_SUMO_rev_2 | 587 | 594 | PF00179 | 0.755 |
TRG_DiLeu_BaEn_2 | 473 | 479 | PF01217 | 0.519 |
TRG_DiLeu_BaEn_4 | 317 | 323 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.403 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 597 | 600 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 229 | 234 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAX7 | Leptomonas seymouri | 47% | 100% |
A0A3S5H6Q1 | Leishmania donovani | 89% | 100% |
A0A422P493 | Trypanosoma rangeli | 37% | 100% |
A4H7D0 | Leishmania braziliensis | 73% | 96% |
A4HVS7 | Leishmania infantum | 89% | 100% |
E9APH3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |