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: A4HHY1
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:0009987 | cellular process | 1 | 12 |
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: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:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0010165 | response to X-ray | 5 | 1 |
GO:0010212 | response to ionizing radiation | 4 | 1 |
GO:0010332 | response to gamma radiation | 5 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071478 | cellular response to radiation | 4 | 1 |
GO:0071479 | cellular response to ionizing radiation | 5 | 1 |
GO:0071480 | cellular response to gamma radiation | 6 | 1 |
GO:0071481 | cellular response to X-ray | 6 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
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 | 0.559 |
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 743 | 747 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 786 | 790 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.194 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 743 | 745 | PF00675 | 0.359 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.302 |
CLV_PCSK_PC7_1 | 126 | 132 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.308 |
DEG_SCF_FBW7_1 | 572 | 577 | PF00400 | 0.458 |
DOC_CKS1_1 | 290 | 295 | PF01111 | 0.379 |
DOC_CYCLIN_RxL_1 | 481 | 492 | PF00134 | 0.329 |
DOC_CYCLIN_yCln2_LP_2 | 223 | 229 | PF00134 | 0.535 |
DOC_MAPK_DCC_7 | 416 | 425 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 130 | 138 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 305 | 313 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 332 | 342 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 305 | 313 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 65 | 73 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 775 | 784 | PF00069 | 0.577 |
DOC_MAPK_NFAT4_5 | 775 | 783 | PF00069 | 0.319 |
DOC_PIKK_1 | 446 | 453 | PF02985 | 0.532 |
DOC_PP1_RVXF_1 | 428 | 435 | PF00149 | 0.536 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.505 |
DOC_PP4_FxxP_1 | 736 | 739 | PF00568 | 0.559 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.379 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.737 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 570 | 575 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 104 | 113 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 257 | 265 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 29 | 37 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 433 | 440 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 514 | 521 | PF00244 | 0.519 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 516 | 520 | PF00533 | 0.489 |
LIG_Clathr_ClatBox_1 | 153 | 157 | PF01394 | 0.287 |
LIG_CSL_BTD_1 | 736 | 739 | PF09270 | 0.476 |
LIG_eIF4E_1 | 715 | 721 | PF01652 | 0.515 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.270 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.452 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.540 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.464 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.342 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.535 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.521 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.528 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.533 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.481 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.601 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.525 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.476 |
LIG_FHA_2 | 752 | 758 | PF00498 | 0.479 |
LIG_FHA_2 | 765 | 771 | PF00498 | 0.479 |
LIG_FHA_2 | 786 | 792 | PF00498 | 0.654 |
LIG_GBD_Chelix_1 | 600 | 608 | PF00786 | 0.475 |
LIG_LIR_Apic_2 | 287 | 293 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 733 | 739 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 107 | 118 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 525 | 533 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 567 | 574 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 654 | 663 | PF02991 | 0.515 |
LIG_LIR_LC3C_4 | 165 | 168 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 107 | 113 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 567 | 572 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 735 | 740 | PF02991 | 0.540 |
LIG_LYPXL_yS_3 | 437 | 440 | PF13949 | 0.673 |
LIG_MYND_1 | 507 | 511 | PF01753 | 0.625 |
LIG_NBox_RRM_1 | 112 | 122 | PF00076 | 0.540 |
LIG_PCNA_yPIPBox_3 | 371 | 381 | PF02747 | 0.533 |
LIG_PCNA_yPIPBox_3 | 471 | 484 | PF02747 | 0.460 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.404 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.418 |
LIG_SH2_NCK_1 | 528 | 532 | PF00017 | 0.561 |
LIG_SH2_PTP2 | 290 | 293 | PF00017 | 0.559 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 716 | 720 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 740 | 743 | PF00017 | 0.559 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.571 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.467 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.536 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.463 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.559 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.421 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.402 |
LIG_Sin3_3 | 373 | 380 | PF02671 | 0.559 |
LIG_SUMO_SIM_anti_2 | 162 | 168 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 231 | 237 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 6 | 11 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 4 | 11 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.379 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.531 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.379 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.479 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.559 |
LIG_TRAF2_1 | 546 | 549 | PF00917 | 0.482 |
LIG_TRAF2_1 | 754 | 757 | PF00917 | 0.555 |
LIG_UBA3_1 | 604 | 609 | PF00899 | 0.474 |
LIG_WRC_WIRS_1 | 652 | 657 | PF05994 | 0.479 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.521 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.524 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.696 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.620 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.650 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.478 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.505 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.511 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.481 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.497 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.502 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.479 |
MOD_CK2_1 | 764 | 770 | PF00069 | 0.479 |
MOD_GlcNHglycan | 193 | 197 | PF01048 | 0.649 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.252 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.341 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.501 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.533 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.321 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.552 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.722 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.308 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.629 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.591 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.659 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.719 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.314 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.251 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.733 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.446 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.445 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.474 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.433 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.479 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.555 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.465 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.500 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.557 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.723 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.671 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.459 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.626 |
MOD_N-GLC_1 | 615 | 620 | PF02516 | 0.484 |
MOD_N-GLC_2 | 133 | 135 | PF02516 | 0.324 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.436 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.477 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.540 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.540 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.540 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.482 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.576 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.486 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.531 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.710 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.513 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.323 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.760 |
MOD_PIKK_1 | 706 | 712 | PF00454 | 0.476 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.515 |
MOD_PKA_1 | 744 | 750 | PF00069 | 0.490 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.559 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.314 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.498 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.531 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.531 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.427 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.536 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.453 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.595 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.445 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.426 |
MOD_Plk_2-3 | 455 | 461 | PF00069 | 0.494 |
MOD_Plk_2-3 | 523 | 529 | PF00069 | 0.584 |
MOD_Plk_2-3 | 785 | 791 | PF00069 | 0.603 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.466 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.466 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.289 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.498 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.413 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.545 |
MOD_Plk_4 | 574 | 580 | PF00069 | 0.692 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.537 |
MOD_Plk_4 | 768 | 774 | PF00069 | 0.379 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.504 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.457 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.475 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.508 |
MOD_ProDKin_1 | 570 | 576 | PF00069 | 0.658 |
MOD_SUMO_for_1 | 304 | 307 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 195 | 204 | PF00179 | 0.618 |
MOD_SUMO_rev_2 | 322 | 331 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 491 | 495 | PF00179 | 0.568 |
TRG_DiLeu_BaEn_1 | 349 | 354 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_1 | 550 | 555 | PF01217 | 0.680 |
TRG_DiLeu_BaEn_2 | 107 | 113 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_2 | 149 | 155 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_2 | 337 | 343 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_4 | 21 | 27 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 396 | 401 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 508 | 513 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.559 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.551 |
TRG_NES_CRM1_1 | 111 | 124 | PF08389 | 0.540 |
TRG_NES_CRM1_1 | 447 | 460 | PF08389 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 301 | 306 | PF00026 | 0.179 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUA9 | Leptomonas seymouri | 56% | 100% |
A0A0S4JHV4 | Bodo saltans | 27% | 96% |
A0A1X0P2Y5 | Trypanosomatidae | 29% | 94% |
A0A3Q8IRQ2 | Leishmania donovani | 78% | 99% |
A0A422NMK3 | Trypanosoma rangeli | 33% | 100% |
A4I561 | Leishmania infantum | 78% | 99% |
C9ZQI7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9B0F8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |
P27641 | Mus musculus | 24% | 100% |
Q2H6C5 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 23% | 100% |
Q4Q7S5 | Leishmania major | 77% | 100% |
Q54LY5 | Dictyostelium discoideum | 22% | 99% |
V5BGZ6 | Trypanosoma cruzi | 33% | 100% |