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:0032991 | protein-containing complex | 1 | 12 |
GO:0043564 | Ku70:Ku80 complex | 3 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0005694 | chromosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q7S5
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006302 | double-strand break repair | 6 | 12 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 12 |
GO:0006310 | DNA recombination | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009314 | response to radiation | 3 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010165 | response to X-ray | 5 | 2 |
GO:0010212 | response to ionizing radiation | 4 | 2 |
GO:0010332 | response to gamma radiation | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0032200 | telomere organization | 6 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 2 |
GO:0071478 | cellular response to radiation | 4 | 2 |
GO:0071479 | cellular response to ionizing radiation | 5 | 2 |
GO:0071480 | cellular response to gamma radiation | 6 | 2 |
GO:0071481 | cellular response to X-ray | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:0104004 | cellular response to environmental stimulus | 3 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003684 | damaged DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042162 | telomeric DNA binding | 6 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043565 | sequence-specific DNA binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 623 | 627 | PF00656 | 0.681 |
CLV_C14_Caspase3-7 | 687 | 691 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 743 | 747 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.361 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 770 | 774 | PF00082 | 0.303 |
CLV_Separin_Metazoa | 682 | 686 | PF03568 | 0.572 |
DEG_APCC_DBOX_1 | 481 | 489 | PF00400 | 0.485 |
DEG_COP1_1 | 188 | 196 | PF00400 | 0.457 |
DEG_ODPH_VHL_1 | 83 | 95 | PF01847 | 0.505 |
DOC_CDC14_PxL_1 | 434 | 442 | PF14671 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 223 | 229 | PF00134 | 0.540 |
DOC_MAPK_DCC_7 | 416 | 425 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 130 | 138 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 239 | 249 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 332 | 342 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 384 | 391 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 482 | 490 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 775 | 784 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 161 | 168 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 384 | 391 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 775 | 784 | PF00069 | 0.661 |
DOC_PIKK_1 | 446 | 453 | PF02985 | 0.614 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.572 |
DOC_PP1_RVXF_1 | 428 | 435 | PF00149 | 0.542 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.491 |
DOC_PP4_FxxP_1 | 736 | 739 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.380 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.734 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 257 | 265 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 29 | 37 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 390 | 399 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 433 | 440 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 482 | 490 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 514 | 521 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 672 | 687 | PF00022 | 0.472 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.427 |
LIG_BIR_III_2 | 396 | 400 | PF00653 | 0.504 |
LIG_BRCT_BRCA1_1 | 516 | 520 | PF00533 | 0.499 |
LIG_Clathr_ClatBox_1 | 720 | 724 | PF01394 | 0.505 |
LIG_CSL_BTD_1 | 736 | 739 | PF09270 | 0.478 |
LIG_DLG_GKlike_1 | 270 | 278 | PF00625 | 0.505 |
LIG_eIF4E_1 | 715 | 721 | PF01652 | 0.517 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.683 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.542 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.685 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.502 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.672 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.611 |
LIG_FHA_2 | 621 | 627 | PF00498 | 0.772 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.519 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.478 |
LIG_FHA_2 | 752 | 758 | PF00498 | 0.481 |
LIG_FHA_2 | 785 | 791 | PF00498 | 0.624 |
LIG_GBD_Chelix_1 | 6 | 14 | PF00786 | 0.395 |
LIG_LIR_Apic_2 | 733 | 739 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 172 | 180 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 525 | 533 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 654 | 663 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 678 | 688 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 678 | 684 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 735 | 740 | PF02991 | 0.541 |
LIG_LYPXL_yS_3 | 437 | 440 | PF13949 | 0.561 |
LIG_MYND_1 | 507 | 511 | PF01753 | 0.620 |
LIG_NBox_RRM_1 | 112 | 122 | PF00076 | 0.542 |
LIG_PCNA_yPIPBox_3 | 471 | 484 | PF02747 | 0.460 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.406 |
LIG_SH2_GRB2like | 715 | 718 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 528 | 532 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 290 | 293 | PF00017 | 0.561 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.539 |
LIG_SH2_SRC | 569 | 572 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.598 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 740 | 743 | PF00017 | 0.561 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.569 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.538 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.464 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.561 |
LIG_SH3_4 | 566 | 573 | PF00018 | 0.619 |
LIG_Sin3_3 | 373 | 380 | PF02671 | 0.561 |
LIG_SUMO_SIM_anti_2 | 150 | 157 | PF11976 | 0.580 |
LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 232 | 237 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 40 | 47 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 5 | 11 | PF11976 | 0.379 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.481 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.561 |
LIG_TRAF2_1 | 444 | 447 | PF00917 | 0.484 |
LIG_TRAF2_1 | 754 | 757 | PF00917 | 0.557 |
LIG_TYR_ITIM | 288 | 293 | PF00017 | 0.533 |
LIG_WRC_WIRS_1 | 652 | 657 | PF05994 | 0.481 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.519 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.713 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.620 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.505 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.636 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.486 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.510 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.525 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.495 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.655 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.481 |
MOD_Cter_Amidation | 561 | 564 | PF01082 | 0.497 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.618 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.357 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.305 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.503 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.525 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.499 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.538 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.322 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.651 |
MOD_GlcNHglycan | 615 | 620 | PF01048 | 0.703 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.670 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.253 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.686 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.444 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.481 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.452 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.464 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.536 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.479 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.633 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.528 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.469 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.745 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.667 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.505 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.675 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.595 |
MOD_N-GLC_2 | 133 | 135 | PF02516 | 0.326 |
MOD_N-GLC_2 | 25 | 27 | PF02516 | 0.299 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.427 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.734 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.481 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.542 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.525 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.554 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.515 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.493 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.575 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.487 |
MOD_NEK2_2 | 477 | 482 | PF00069 | 0.440 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.533 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.713 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.512 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.564 |
MOD_PIKK_1 | 706 | 712 | PF00454 | 0.478 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.517 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.505 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.561 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.499 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.535 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.533 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.528 |
MOD_PKA_2 | 684 | 690 | PF00069 | 0.464 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.444 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.647 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.490 |
MOD_Plk_1 | 459 | 465 | PF00069 | 0.472 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.335 |
MOD_Plk_2-3 | 151 | 157 | PF00069 | 0.457 |
MOD_Plk_2-3 | 455 | 461 | PF00069 | 0.494 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.391 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.597 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.454 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.443 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.458 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.498 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.695 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.513 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.615 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.668 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.705 |
MOD_SUMO_for_1 | 304 | 307 | PF00179 | 0.561 |
MOD_SUMO_for_1 | 721 | 724 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 195 | 204 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_1 | 550 | 555 | PF01217 | 0.675 |
TRG_DiLeu_BaEn_2 | 107 | 113 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_2 | 337 | 343 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.561 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 111 | 124 | PF08389 | 0.542 |
TRG_NES_CRM1_1 | 447 | 461 | PF08389 | 0.580 |
TRG_NLS_MonoExtC_3 | 562 | 567 | PF00514 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.343 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUA9 | Leptomonas seymouri | 57% | 100% |
A0A0S4JHV4 | Bodo saltans | 27% | 97% |
A0A1X0P2Y5 | Trypanosomatidae | 30% | 95% |
A0A3Q8IRQ2 | Leishmania donovani | 92% | 100% |
A0A422NMK3 | Trypanosoma rangeli | 35% | 100% |
A4HHY1 | Leishmania braziliensis | 77% | 100% |
A4I561 | Leishmania infantum | 92% | 100% |
C9ZQI7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9B0F8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q54LY5 | Dictyostelium discoideum | 20% | 100% |
Q75IP6 | Oryza sativa subsp. japonica | 22% | 100% |
Q7RX73 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 20% | 100% |
V5BGZ6 | Trypanosoma cruzi | 34% | 100% |