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: A0A3S5H6Q1
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031848 | protection from non-homologous end joining at telomere | 6 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0036297 | interstrand cross-link repair | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043247 | telomere maintenance in response to DNA damage | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0035312 | 5'-3' DNA exonuclease activity | 7 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.681 |
CLV_C14_Caspase3-7 | 580 | 584 | PF00656 | 0.759 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 765 | 769 | PF00656 | 0.700 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.717 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.712 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.734 |
DEG_APCC_DBOX_1 | 556 | 564 | PF00400 | 0.519 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.514 |
DEG_SCF_FBW7_1 | 249 | 254 | PF00400 | 0.691 |
DEG_SPOP_SBC_1 | 251 | 255 | PF00917 | 0.729 |
DEG_SPOP_SBC_1 | 639 | 643 | PF00917 | 0.702 |
DOC_ANK_TNKS_1 | 667 | 674 | PF00023 | 0.690 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.504 |
DOC_CYCLIN_RxL_1 | 56 | 67 | PF00134 | 0.477 |
DOC_CYCLIN_yCln2_LP_2 | 110 | 116 | PF00134 | 0.391 |
DOC_CYCLIN_yCln2_LP_2 | 478 | 484 | PF00134 | 0.441 |
DOC_MAPK_DCC_7 | 400 | 410 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 70 | 78 | PF00069 | 0.417 |
DOC_MAPK_HePTP_8 | 497 | 509 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 266 | 275 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 401 | 410 | PF00069 | 0.627 |
DOC_MAPK_MEF2A_6 | 500 | 509 | PF00069 | 0.624 |
DOC_MAPK_MEF2A_6 | 70 | 78 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 744 | 751 | PF00069 | 0.653 |
DOC_MAPK_RevD_3 | 6 | 20 | PF00069 | 0.443 |
DOC_PP2B_LxvP_1 | 505 | 508 | PF13499 | 0.646 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.531 |
DOC_PP2B_PxIxI_1 | 405 | 411 | PF00149 | 0.520 |
DOC_PP4_FxxP_1 | 114 | 117 | PF00568 | 0.395 |
DOC_PP4_FxxP_1 | 634 | 637 | PF00568 | 0.795 |
DOC_PP4_MxPP_1 | 600 | 603 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.683 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 305 | 310 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 444 | 452 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 480 | 485 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 675 | 680 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 721 | 729 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 81 | 85 | PF00244 | 0.440 |
LIG_BIR_III_4 | 241 | 245 | PF00653 | 0.573 |
LIG_eIF4E_1 | 542 | 548 | PF01652 | 0.520 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.494 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.397 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.677 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.603 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.706 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.747 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.682 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.786 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.444 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.601 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.454 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.498 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.706 |
LIG_HCF-1_HBM_1 | 160 | 163 | PF13415 | 0.410 |
LIG_Integrin_isoDGR_2 | 381 | 383 | PF01839 | 0.518 |
LIG_KLC1_Yacidic_2 | 160 | 165 | PF13176 | 0.406 |
LIG_LIR_Gen_1 | 165 | 176 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 300 | 310 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 474 | 482 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 11 | 16 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 474 | 478 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 682 | 686 | PF02991 | 0.469 |
LIG_NRBOX | 202 | 208 | PF00104 | 0.565 |
LIG_NRBOX | 564 | 570 | PF00104 | 0.464 |
LIG_PCNA_PIPBox_1 | 147 | 156 | PF02747 | 0.477 |
LIG_PDZ_Class_2 | 767 | 772 | PF00595 | 0.773 |
LIG_Pex14_1 | 47 | 51 | PF04695 | 0.354 |
LIG_Pex14_2 | 31 | 35 | PF04695 | 0.537 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.494 |
LIG_SH2_CRK | 435 | 439 | PF00017 | 0.426 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.434 |
LIG_SH2_SRC | 542 | 545 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.494 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.642 |
LIG_SH3_1 | 538 | 544 | PF00018 | 0.580 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.713 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.582 |
LIG_SUMO_SIM_anti_2 | 474 | 480 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 562 | 567 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 305 | 311 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 4 | 12 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 480 | 485 | PF11976 | 0.485 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.508 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.541 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.511 |
LIG_TRAF2_1 | 584 | 587 | PF00917 | 0.706 |
LIG_TYR_ITIM | 105 | 110 | PF00017 | 0.440 |
LIG_TYR_ITSM | 430 | 437 | PF00017 | 0.576 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.507 |
LIG_WRC_WIRS_1 | 362 | 367 | PF05994 | 0.473 |
MOD_CDC14_SPxK_1 | 148 | 151 | PF00782 | 0.467 |
MOD_CDC14_SPxK_1 | 327 | 330 | PF00782 | 0.628 |
MOD_CDK_SPK_2 | 635 | 640 | PF00069 | 0.583 |
MOD_CDK_SPxK_1 | 145 | 151 | PF00069 | 0.487 |
MOD_CDK_SPxK_1 | 324 | 330 | PF00069 | 0.606 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.474 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.731 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.597 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.505 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.455 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.758 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.815 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.680 |
MOD_CK1_1 | 752 | 758 | PF00069 | 0.737 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.464 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.600 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.591 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.454 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.577 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.516 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.478 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.570 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.723 |
MOD_Cter_Amidation | 17 | 20 | PF01082 | 0.565 |
MOD_Cter_Amidation | 219 | 222 | PF01082 | 0.453 |
MOD_Cter_Amidation | 699 | 702 | PF01082 | 0.828 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.415 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.442 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.659 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.632 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.793 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.614 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.496 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.680 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.591 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.366 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.584 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.722 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.721 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.729 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.790 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.749 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.541 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.452 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.387 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.653 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.754 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.676 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.404 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.724 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.366 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.460 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.460 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.453 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.736 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.649 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.702 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.728 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.828 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.553 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.632 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.725 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.466 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.630 |
MOD_LATS_1 | 39 | 45 | PF00433 | 0.568 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.766 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.485 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.492 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.334 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.456 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.288 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.392 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.698 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.551 |
MOD_NEK2_1 | 750 | 755 | PF00069 | 0.749 |
MOD_NEK2_2 | 149 | 154 | PF00069 | 0.469 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.632 |
MOD_NEK2_2 | 723 | 728 | PF00069 | 0.594 |
MOD_OFUCOSY | 687 | 692 | PF10250 | 0.507 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.601 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.507 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.729 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.586 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.716 |
MOD_PK_1 | 480 | 486 | PF00069 | 0.427 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.450 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.698 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.516 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.620 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.576 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.696 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.405 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.418 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.706 |
MOD_Plk_1 | 661 | 667 | PF00069 | 0.702 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.431 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.466 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.401 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.564 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.649 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.723 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.334 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.487 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.439 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.773 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.721 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.681 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.548 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.451 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.462 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.709 |
MOD_SUMO_for_1 | 727 | 730 | PF00179 | 0.669 |
MOD_SUMO_rev_2 | 314 | 323 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 580 | 589 | PF00179 | 0.734 |
TRG_DiLeu_BaEn_2 | 470 | 476 | PF01217 | 0.566 |
TRG_DiLeu_BaEn_4 | 315 | 321 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 302 | 307 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.613 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.787 |
TRG_ER_diArg_1 | 593 | 596 | PF00400 | 0.784 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 227 | 232 | PF00026 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 295 | 299 | PF00026 | 0.560 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAX7 | Leptomonas seymouri | 49% | 100% |
A0A422P493 | Trypanosoma rangeli | 37% | 100% |
A4H7D0 | Leishmania braziliensis | 74% | 100% |
A4HVS7 | Leishmania infantum | 100% | 100% |
E9APH3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QG05 | Leishmania major | 89% | 100% |