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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4IA93
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
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:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic 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: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:0051276 | chromosome organization | 5 | 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 | 446 | 450 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 698 | 702 | PF00656 | 0.701 |
CLV_MEL_PAP_1 | 654 | 660 | PF00089 | 0.512 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 487 | 489 | PF00082 | 0.478 |
CLV_PCSK_PC1ET2_1 | 592 | 594 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 733 | 735 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 772 | 774 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.559 |
CLV_Separin_Metazoa | 328 | 332 | PF03568 | 0.466 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.381 |
DEG_APCC_DBOX_1 | 735 | 743 | PF00400 | 0.444 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.689 |
DEG_SCF_FBW7_1 | 754 | 761 | PF00400 | 0.487 |
DEG_SPOP_SBC_1 | 746 | 750 | PF00917 | 0.558 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.368 |
DOC_CYCLIN_RxL_1 | 292 | 301 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 354 | 362 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 369 | 376 | PF00069 | 0.232 |
DOC_MAPK_MEF2A_6 | 297 | 304 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 369 | 376 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.288 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.506 |
DOC_PP2B_LxvP_1 | 606 | 609 | PF13499 | 0.442 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.333 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.334 |
DOC_PP4_FxxP_1 | 542 | 545 | PF00568 | 0.335 |
DOC_PP4_FxxP_1 | 625 | 628 | PF00568 | 0.442 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 756 | 760 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.505 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 776 | 781 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 252 | 256 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 439 | 445 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 501 | 508 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 607 | 616 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 666 | 671 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.280 |
LIG_BIR_III_2 | 378 | 382 | PF00653 | 0.485 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.338 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.469 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.386 |
LIG_CtBP_PxDLS_1 | 148 | 152 | PF00389 | 0.245 |
LIG_deltaCOP1_diTrp_1 | 240 | 245 | PF00928 | 0.398 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.300 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.416 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.579 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.461 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.583 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.589 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.569 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.745 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.543 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.543 |
LIG_Integrin_isoDGR_2 | 250 | 252 | PF01839 | 0.420 |
LIG_LIR_Apic_2 | 144 | 148 | PF02991 | 0.248 |
LIG_LIR_Apic_2 | 254 | 258 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 306 | 312 | PF02991 | 0.321 |
LIG_LIR_Apic_2 | 540 | 545 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 624 | 628 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 240 | 246 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 417 | 427 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 548 | 558 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 577 | 587 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 621 | 629 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 665 | 676 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 765 | 776 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 101 | 105 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 429 | 435 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 577 | 582 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 621 | 625 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 665 | 671 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 765 | 771 | PF02991 | 0.693 |
LIG_MYND_1 | 469 | 473 | PF01753 | 0.412 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.319 |
LIG_PCNA_yPIPBox_3 | 17 | 25 | PF02747 | 0.489 |
LIG_PCNA_yPIPBox_3 | 292 | 303 | PF02747 | 0.449 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.266 |
LIG_Pex14_2 | 316 | 320 | PF04695 | 0.463 |
LIG_Pex14_2 | 428 | 432 | PF04695 | 0.423 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.278 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.444 |
LIG_SH2_CRK | 419 | 423 | PF00017 | 0.432 |
LIG_SH2_CRK | 551 | 555 | PF00017 | 0.498 |
LIG_SH2_CRK | 579 | 583 | PF00017 | 0.535 |
LIG_SH2_PTP2 | 255 | 258 | PF00017 | 0.522 |
LIG_SH2_SRC | 255 | 258 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 579 | 583 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 643 | 647 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.360 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.485 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.449 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.382 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.497 |
LIG_SH3_3 | 710 | 716 | PF00018 | 0.562 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 301 | 306 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 580 | 586 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 301 | 306 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 36 | 41 | PF11976 | 0.242 |
LIG_SUMO_SIM_par_1 | 472 | 478 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 564 | 570 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 580 | 586 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 804 | 812 | PF11976 | 0.593 |
LIG_TRAF2_1 | 784 | 787 | PF00917 | 0.596 |
LIG_TYR_ITIM | 549 | 554 | PF00017 | 0.315 |
MOD_CDC14_SPxK_1 | 415 | 418 | PF00782 | 0.362 |
MOD_CDK_SPxK_1 | 412 | 418 | PF00069 | 0.336 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.277 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.475 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.431 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.605 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.694 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.611 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.669 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.617 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.531 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.582 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.628 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.529 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.447 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.361 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.703 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.422 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.399 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.624 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.629 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.760 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.720 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.589 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.704 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.605 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.643 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.627 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.235 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.262 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.391 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.350 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.298 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.546 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.631 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.677 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.334 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.571 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.628 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.682 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.659 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.650 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.513 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.385 |
MOD_N-GLC_1 | 523 | 528 | PF02516 | 0.587 |
MOD_N-GLC_2 | 209 | 211 | PF02516 | 0.314 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.412 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.343 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.368 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.454 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.325 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.582 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.516 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.507 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.631 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.564 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.645 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.414 |
MOD_PIKK_1 | 31 | 37 | PF00454 | 0.288 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.476 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.613 |
MOD_PK_1 | 666 | 672 | PF00069 | 0.676 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.277 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.459 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.462 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.427 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.585 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.657 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.544 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.655 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.668 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.576 |
MOD_PKB_1 | 486 | 494 | PF00069 | 0.487 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.402 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.298 |
MOD_Plk_2-3 | 529 | 535 | PF00069 | 0.497 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.305 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.379 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.330 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.308 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.537 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.352 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.284 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.273 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.489 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.591 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.389 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.366 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.466 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.584 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.636 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.525 |
MOD_ProDKin_1 | 776 | 782 | PF00069 | 0.775 |
TRG_DiLeu_BaEn_1 | 534 | 539 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_1 | 601 | 606 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_2 | 617 | 623 | PF01217 | 0.266 |
TRG_DiLeu_BaLyEn_6 | 201 | 206 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 486 | 489 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 652 | 655 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 731 | 734 | PF00400 | 0.710 |
TRG_NES_CRM1_1 | 662 | 677 | PF08389 | 0.518 |
TRG_NLS_MonoExtC_3 | 731 | 736 | PF00514 | 0.738 |
TRG_NLS_MonoExtN_4 | 732 | 737 | PF00514 | 0.758 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB91 | Leptomonas seymouri | 44% | 93% |
A0A0S4INP1 | Bodo saltans | 26% | 100% |
A0A1X0P9Y1 | Trypanosomatidae | 31% | 100% |
A0A3Q8IHR3 | Leishmania donovani | 99% | 100% |
A0A3R7MJM0 | Trypanosoma rangeli | 31% | 100% |
A4HB44 | Leishmania braziliensis | 66% | 98% |
C9ZM02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B5B5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q2L8 | Leishmania major | 90% | 100% |
V5BQH0 | Trypanosoma cruzi | 32% | 100% |