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 |
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: A4HZ62
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
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 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003684 | damaged DNA binding | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
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 | 342 | 346 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 563 | 567 | PF00656 | 0.584 |
CLV_C14_Caspase3-7 | 593 | 597 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 356 | 360 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.647 |
CLV_PCSK_PC7_1 | 353 | 359 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.605 |
CLV_Separin_Metazoa | 201 | 205 | PF03568 | 0.605 |
CLV_Separin_Metazoa | 424 | 428 | PF03568 | 0.496 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.605 |
DEG_SCF_FBW7_1 | 530 | 537 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.483 |
DEG_SPOP_SBC_1 | 667 | 671 | PF00917 | 0.460 |
DOC_CYCLIN_RxL_1 | 230 | 241 | PF00134 | 0.605 |
DOC_MAPK_gen_1 | 427 | 433 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 451 | 459 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 646 | 656 | PF00069 | 0.501 |
DOC_MAPK_RevD_3 | 167 | 181 | PF00069 | 0.503 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.454 |
DOC_PP2B_LxvP_1 | 723 | 726 | PF13499 | 0.660 |
DOC_PP2B_LxvP_1 | 728 | 731 | PF13499 | 0.591 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.605 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.564 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 289 | 298 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 451 | 456 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 551 | 556 | PF00244 | 0.623 |
LIG_APCC_ABBAyCdc20_2 | 248 | 254 | PF00400 | 0.495 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.587 |
LIG_BIR_III_4 | 348 | 352 | PF00653 | 0.690 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.605 |
LIG_BRCT_BRCA1_1 | 291 | 295 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.488 |
LIG_eIF4E_1 | 230 | 236 | PF01652 | 0.605 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.475 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.520 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.455 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.544 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.518 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.494 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.555 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.485 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.503 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.610 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.655 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.583 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.513 |
LIG_FHA_1 | 738 | 744 | PF00498 | 0.602 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.518 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.512 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 325 | 330 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 137 | 147 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 23 | 34 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 439 | 448 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 673 | 682 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 673 | 679 | PF02991 | 0.463 |
LIG_PCNA_PIPBox_1 | 553 | 562 | PF02747 | 0.541 |
LIG_PCNA_yPIPBox_3 | 547 | 560 | PF02747 | 0.590 |
LIG_PTB_Apo_2 | 458 | 465 | PF02174 | 0.549 |
LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 140 | 143 | PF00017 | 0.605 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.605 |
LIG_SH2_STAP1 | 257 | 261 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.403 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.488 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.579 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.488 |
LIG_SH3_3 | 712 | 718 | PF00018 | 0.781 |
LIG_SH3_3 | 729 | 735 | PF00018 | 0.474 |
LIG_SH3_4 | 278 | 285 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 624 | 631 | PF11976 | 0.685 |
LIG_SUMO_SIM_anti_2 | 740 | 746 | PF11976 | 0.634 |
LIG_SUMO_SIM_anti_2 | 753 | 760 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 41 | 46 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 429 | 436 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 473 | 479 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 624 | 631 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 739 | 746 | PF11976 | 0.603 |
LIG_SUMO_SIM_par_1 | 79 | 84 | PF11976 | 0.516 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.431 |
LIG_TRAF2_1 | 686 | 689 | PF00917 | 0.653 |
LIG_UBA3_1 | 675 | 684 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 556 | 561 | PF05994 | 0.624 |
LIG_WRC_WIRS_1 | 609 | 614 | PF05994 | 0.470 |
MOD_CDK_SPxxK_3 | 81 | 88 | PF00069 | 0.379 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.385 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.372 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.592 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.524 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.514 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.364 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.493 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.272 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.358 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.473 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.621 |
MOD_Cter_Amidation | 354 | 357 | PF01082 | 0.627 |
MOD_Cter_Amidation | 362 | 365 | PF01082 | 0.583 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.394 |
MOD_GlcNHglycan | 258 | 262 | PF01048 | 0.337 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.411 |
MOD_GlcNHglycan | 288 | 292 | PF01048 | 0.328 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.450 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.319 |
MOD_GlcNHglycan | 519 | 523 | PF01048 | 0.363 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.633 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.646 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.684 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.681 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.603 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.501 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.394 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.604 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.317 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.303 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.333 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.364 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.473 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.662 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.781 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.658 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.598 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.691 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.635 |
MOD_LATS_1 | 449 | 455 | PF00433 | 0.303 |
MOD_LATS_1 | 549 | 555 | PF00433 | 0.663 |
MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.228 |
MOD_N-GLC_1 | 597 | 602 | PF02516 | 0.785 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.303 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.462 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.343 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.303 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.374 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.647 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.650 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.527 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.242 |
MOD_OFUCOSY | 335 | 341 | PF10250 | 0.581 |
MOD_OGLYCOS | 657 | 662 | PF02709 | 0.558 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.325 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.265 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.457 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.318 |
MOD_PKA_1 | 64 | 70 | PF00069 | 0.364 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.501 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.389 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.318 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.376 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.450 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.379 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.228 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.272 |
MOD_Plk_2-3 | 754 | 760 | PF00069 | 0.676 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.397 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.417 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.268 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.501 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.541 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.657 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.694 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.504 |
MOD_Plk_4 | 754 | 760 | PF00069 | 0.658 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.318 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.489 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.501 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.582 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.724 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.634 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.585 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.640 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.403 |
TRG_AP2beta_CARGO_1 | 442 | 451 | PF09066 | 0.318 |
TRG_DiLeu_BaEn_1 | 232 | 237 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_4 | 442 | 448 | PF01217 | 0.318 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.298 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 391 | 394 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.513 |
TRG_NES_CRM1_1 | 479 | 493 | PF08389 | 0.379 |
TRG_NLS_MonoCore_2 | 355 | 360 | PF00514 | 0.645 |
TRG_NLS_MonoExtC_3 | 355 | 360 | PF00514 | 0.696 |
TRG_NLS_MonoExtN_4 | 353 | 360 | PF00514 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 175 | 179 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NXK7 | Trypanosomatidae | 42% | 100% |
A4HBR0 | Leishmania braziliensis | 78% | 100% |
D0A1I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E8NHQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QCF2 | Leishmania major | 93% | 100% |