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. | yes | yes: 15 |
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005657 | replication fork | 2 | 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 |
Related structures:
AlphaFold database: A4HBX5
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 13 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 13 |
GO:0006259 | DNA metabolic process | 4 | 13 |
GO:0006281 | DNA repair | 5 | 13 |
GO:0006310 | DNA recombination | 5 | 13 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0006950 | response to stress | 2 | 13 |
GO:0006974 | DNA damage response | 4 | 13 |
GO:0006996 | organelle organization | 4 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016043 | cellular component organization | 3 | 13 |
GO:0032200 | telomere organization | 6 | 13 |
GO:0033554 | cellular response to stress | 3 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0046483 | heterocycle metabolic process | 3 | 13 |
GO:0050896 | response to stimulus | 1 | 13 |
GO:0051276 | chromosome organization | 5 | 13 |
GO:0051716 | cellular response to stimulus | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:0071840 | cellular component organization or biogenesis | 2 | 13 |
GO:0090304 | nucleic acid metabolic process | 4 | 13 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 13 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003678 | DNA helicase activity | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 13 |
GO:0016462 | pyrophosphatase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 13 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 13 |
GO:0016887 | ATP hydrolysis activity | 7 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0000287 | magnesium ion binding | 5 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.727 |
CLV_MEL_PAP_1 | 503 | 509 | PF00089 | 0.533 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 634 | 636 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 634 | 636 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.717 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.465 |
DOC_MAPK_DCC_7 | 599 | 608 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 634 | 641 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 678 | 687 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 93 | 100 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 599 | 608 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 634 | 641 | PF00069 | 0.363 |
DOC_PP1_RVXF_1 | 244 | 250 | PF00149 | 0.584 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.304 |
DOC_SPAK_OSR1_1 | 506 | 510 | PF12202 | 0.520 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 697 | 701 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.716 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.510 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.370 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 318 | 327 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 397 | 401 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 408 | 418 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 539 | 548 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 607 | 615 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 629 | 633 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 382 | 399 | PF00022 | 0.333 |
LIG_Actin_WH2_2 | 550 | 568 | PF00022 | 0.475 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.468 |
LIG_APCC_ABBAyCdc20_2 | 21 | 27 | PF00400 | 0.476 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.628 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.474 |
LIG_BIR_III_4 | 749 | 753 | PF00653 | 0.492 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.367 |
LIG_BRCT_BRCA1_1 | 533 | 537 | PF00533 | 0.576 |
LIG_CtBP_PxDLS_1 | 759 | 763 | PF00389 | 0.534 |
LIG_DLG_GKlike_1 | 154 | 161 | PF00625 | 0.526 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.368 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.417 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.568 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.393 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.377 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.512 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.481 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.739 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.443 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.462 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.312 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.432 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.427 |
LIG_GBD_Chelix_1 | 392 | 400 | PF00786 | 0.210 |
LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 429 | 436 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 455 | 463 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 542 | 553 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.555 |
LIG_LIR_LC3C_4 | 587 | 592 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.770 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 705 | 709 | PF02991 | 0.480 |
LIG_MAD2 | 394 | 402 | PF02301 | 0.367 |
LIG_PDZ_Class_3 | 783 | 788 | PF00595 | 0.506 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.530 |
LIG_SH2_NCK_1 | 545 | 549 | PF00017 | 0.530 |
LIG_SH2_PTP2 | 673 | 676 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 524 | 527 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.730 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.352 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.682 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.553 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.469 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.483 |
LIG_SH3_3 | 773 | 779 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 371 | 377 | PF11976 | 0.367 |
LIG_SUMO_SIM_anti_2 | 691 | 696 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 371 | 377 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 423 | 429 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 570 | 576 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 758 | 764 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.501 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.480 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.449 |
LIG_TRAF2_1 | 502 | 505 | PF00917 | 0.559 |
LIG_UBA3_1 | 657 | 664 | PF00899 | 0.266 |
MOD_CDK_SPxxK_3 | 485 | 492 | PF00069 | 0.367 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.727 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.696 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.717 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.653 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.432 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.306 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.439 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.437 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.377 |
MOD_CK1_1 | 710 | 716 | PF00069 | 0.590 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.580 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.766 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.737 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.444 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.440 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.491 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.477 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.727 |
MOD_GlcNHglycan | 197 | 201 | PF01048 | 0.754 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.400 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.231 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.540 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.710 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.765 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.638 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.686 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.696 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.637 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.650 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.718 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.482 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.162 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.424 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.655 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.582 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.559 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.799 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.431 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.505 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.478 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.364 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.210 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.423 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.523 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.532 |
MOD_NEK2_1 | 685 | 690 | PF00069 | 0.497 |
MOD_NEK2_1 | 709 | 714 | PF00069 | 0.577 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.462 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.352 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.491 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.426 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.304 |
MOD_NEK2_2 | 561 | 566 | PF00069 | 0.329 |
MOD_NEK2_2 | 643 | 648 | PF00069 | 0.359 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.750 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.359 |
MOD_PK_1 | 94 | 100 | PF00069 | 0.552 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.533 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.808 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.562 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.333 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.419 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.462 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.429 |
MOD_PKA_2 | 628 | 634 | PF00069 | 0.602 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.497 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.387 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.510 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.458 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.462 |
MOD_Plk_1 | 662 | 668 | PF00069 | 0.533 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.498 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.689 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.534 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.210 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.386 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.421 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.526 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.435 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.448 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.595 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.364 |
MOD_SUMO_for_1 | 297 | 300 | PF00179 | 0.469 |
MOD_SUMO_for_1 | 783 | 786 | PF00179 | 0.747 |
TRG_DiLeu_BaEn_1 | 510 | 515 | PF01217 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 482 | 484 | PF00400 | 0.450 |
TRG_NES_CRM1_1 | 651 | 663 | PF08389 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 501 | 505 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JCS0 | Bodo saltans | 41% | 100% |
A0A1X0NZA2 | Trypanosomatidae | 39% | 92% |
A0A3Q8IBY0 | Leishmania donovani | 80% | 100% |
A0A3R7MKN4 | Trypanosoma rangeli | 30% | 82% |
A0A422NAK1 | Trypanosoma rangeli | 49% | 100% |
A4HZ95 | Leishmania infantum | 80% | 100% |
C9ZUJ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 79% |
D0A177 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 99% |
E9AVA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q38CE9 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 45% | 99% |
Q4QC77 | Leishmania major | 81% | 100% |
Q57YG0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 29% | 79% |
Q9UUA2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 98% |
V5B8C2 | Trypanosoma cruzi | 30% | 81% |
V5BE68 | Trypanosoma cruzi | 48% | 100% |