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 |
Related structures:
AlphaFold database: E9APH3
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 | 580 | 584 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 764 | 768 | PF00656 | 0.588 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 753 | 755 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.476 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.409 |
DEG_SPOP_SBC_1 | 251 | 255 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 723 | 727 | PF00917 | 0.526 |
DOC_CKS1_1 | 122 | 127 | PF01111 | 0.441 |
DOC_CYCLIN_RxL_1 | 54 | 65 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.321 |
DOC_CYCLIN_yCln2_LP_2 | 477 | 483 | PF00134 | 0.363 |
DOC_MAPK_DCC_7 | 400 | 409 | PF00069 | 0.508 |
DOC_MAPK_DCC_7 | 590 | 600 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 590 | 600 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 68 | 76 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 701 | 707 | PF00069 | 0.569 |
DOC_MAPK_HePTP_8 | 496 | 508 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 499 | 508 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 701 | 709 | PF00069 | 0.569 |
DOC_MAPK_RevD_3 | 4 | 20 | PF00069 | 0.378 |
DOC_PP2B_LxvP_1 | 504 | 507 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.403 |
DOC_PP2B_PxIxI_1 | 404 | 410 | PF00149 | 0.398 |
DOC_PP4_FxxP_1 | 112 | 115 | PF00568 | 0.326 |
DOC_PP4_FxxP_1 | 634 | 637 | PF00568 | 0.656 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.777 |
DOC_USP7_UBL2_3 | 730 | 734 | PF12436 | 0.526 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.359 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.313 |
LIG_14-3-3_CanoR_1 | 303 | 308 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 443 | 451 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 479 | 484 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 675 | 680 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 753 | 762 | PF00244 | 0.528 |
LIG_BIR_III_4 | 239 | 243 | PF00653 | 0.525 |
LIG_BRCT_BRCA1_1 | 631 | 635 | PF00533 | 0.588 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.374 |
LIG_eIF4E_1 | 541 | 547 | PF01652 | 0.416 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.534 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.367 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.434 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.545 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.305 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.353 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.582 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.504 |
LIG_FHA_1 | 754 | 760 | PF00498 | 0.660 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.351 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.364 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.377 |
LIG_HCF-1_HBM_1 | 158 | 161 | PF13415 | 0.336 |
LIG_KLC1_Yacidic_2 | 158 | 163 | PF13176 | 0.333 |
LIG_LIR_Apic_2 | 621 | 625 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 632 | 637 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 163 | 174 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 473 | 481 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 544 | 551 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 11 | 16 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 163 | 169 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 544 | 548 | PF02991 | 0.328 |
LIG_MLH1_MIPbox_1 | 631 | 635 | PF16413 | 0.588 |
LIG_NRBOX | 200 | 206 | PF00104 | 0.439 |
LIG_PDZ_Class_2 | 766 | 771 | PF00595 | 0.635 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.396 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.365 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.356 |
LIG_SH2_CRK | 622 | 626 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 622 | 626 | PF00017 | 0.462 |
LIG_SH2_PTP2 | 105 | 108 | PF00017 | 0.304 |
LIG_SH2_SRC | 622 | 625 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 223 | 226 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.561 |
LIG_SH3_1 | 537 | 543 | PF00018 | 0.444 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.375 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.499 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.629 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.530 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.509 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.502 |
LIG_SUMO_SIM_anti_2 | 473 | 479 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 303 | 309 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 405 | 412 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 479 | 484 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 5 | 12 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 756 | 764 | PF11976 | 0.584 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.384 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.418 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.392 |
LIG_TRAF2_1 | 584 | 587 | PF00917 | 0.663 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.343 |
LIG_TYR_ITIM | 299 | 304 | PF00017 | 0.299 |
LIG_TYR_ITSM | 429 | 436 | PF00017 | 0.445 |
LIG_WRC_WIRS_1 | 148 | 153 | PF05994 | 0.380 |
LIG_WRC_WIRS_1 | 360 | 365 | PF05994 | 0.392 |
MOD_CDC14_SPxK_1 | 146 | 149 | PF00782 | 0.341 |
MOD_CDK_SPxK_1 | 143 | 149 | PF00069 | 0.362 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.363 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.610 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.496 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.397 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.482 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.457 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.627 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.749 |
MOD_CK1_1 | 691 | 697 | PF00069 | 0.565 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.474 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.476 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.366 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.445 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.395 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.384 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.471 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.542 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.624 |
MOD_Cter_Amidation | 17 | 20 | PF01082 | 0.498 |
MOD_Cter_Amidation | 217 | 220 | PF01082 | 0.409 |
MOD_Cter_Amidation | 699 | 702 | PF01082 | 0.685 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.321 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.398 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.528 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.501 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.654 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.467 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.538 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.374 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.633 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.544 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.402 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.529 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.616 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.522 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.628 |
MOD_GlcNHglycan | 662 | 666 | PF01048 | 0.552 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.567 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.627 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.716 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.480 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.557 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.360 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.388 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.545 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.602 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.277 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.397 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.340 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.397 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.308 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.573 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.641 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.564 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.573 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.803 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.486 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.524 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.590 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.629 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.347 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.545 |
MOD_LATS_1 | 37 | 43 | PF00433 | 0.441 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.640 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.482 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.380 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.343 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.332 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.394 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.369 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.418 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.614 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.518 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.345 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.379 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.518 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.397 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.596 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.509 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.611 |
MOD_PK_1 | 479 | 485 | PF00069 | 0.341 |
MOD_PKA_1 | 753 | 759 | PF00069 | 0.497 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.460 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.395 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.556 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.450 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.521 |
MOD_PKA_2 | 674 | 680 | PF00069 | 0.611 |
MOD_PKA_2 | 753 | 759 | PF00069 | 0.625 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.471 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.349 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.339 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.363 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.349 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.430 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.312 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.661 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.626 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.498 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.433 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.362 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.638 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.601 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.495 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.384 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.370 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.607 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.312 |
MOD_SUMO_rev_2 | 580 | 589 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 731 | 739 | PF00179 | 0.517 |
TRG_DiLeu_BaEn_1 | 314 | 319 | PF01217 | 0.334 |
TRG_DiLeu_BaEn_2 | 469 | 475 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 402 | 407 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 593 | 596 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 225 | 230 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAX7 | Leptomonas seymouri | 48% | 100% |
A0A3S5H6Q1 | Leishmania donovani | 86% | 100% |
A4H7D0 | Leishmania braziliensis | 72% | 100% |
A4HVS7 | Leishmania infantum | 86% | 100% |
Q4QG05 | Leishmania major | 85% | 100% |