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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AT68
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 847 | 849 | PF00675 | 0.516 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 847 | 849 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 786 | 788 | PF00082 | 0.503 |
CLV_PCSK_PC7_1 | 575 | 581 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 665 | 669 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 789 | 793 | PF00082 | 0.501 |
CLV_Separin_Metazoa | 719 | 723 | PF03568 | 0.567 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.433 |
DEG_APCC_DBOX_1 | 786 | 794 | PF00400 | 0.514 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.420 |
DEG_SPOP_SBC_1 | 261 | 265 | PF00917 | 0.430 |
DEG_SPOP_SBC_1 | 553 | 557 | PF00917 | 0.519 |
DOC_CKS1_1 | 780 | 785 | PF01111 | 0.495 |
DOC_CYCLIN_RxL_1 | 133 | 144 | PF00134 | 0.594 |
DOC_CYCLIN_RxL_1 | 223 | 233 | PF00134 | 0.373 |
DOC_CYCLIN_RxL_1 | 662 | 672 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 579 | 587 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 785 | 793 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 126 | 134 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 323 | 331 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 347 | 354 | PF00069 | 0.432 |
DOC_MAPK_NFAT4_5 | 323 | 331 | PF00069 | 0.356 |
DOC_MAPK_RevD_3 | 834 | 848 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 119 | 125 | PF00149 | 0.463 |
DOC_PP1_RVXF_1 | 787 | 793 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.738 |
DOC_PP4_FxxP_1 | 828 | 831 | PF00568 | 0.446 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.477 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.502 |
DOC_USP7_UBL2_3 | 781 | 785 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 779 | 784 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 530 | 538 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 704 | 712 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 722 | 727 | PF00244 | 0.425 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 727 | 731 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 824 | 828 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.531 |
LIG_Clathr_ClatBox_1 | 372 | 376 | PF01394 | 0.420 |
LIG_Clathr_ClatBox_1 | 790 | 794 | PF01394 | 0.507 |
LIG_CSL_BTD_1 | 776 | 779 | PF09270 | 0.592 |
LIG_deltaCOP1_diTrp_1 | 57 | 64 | PF00928 | 0.542 |
LIG_eIF4E_1 | 321 | 327 | PF01652 | 0.503 |
LIG_eIF4E_1 | 348 | 354 | PF01652 | 0.291 |
LIG_FAT_LD_1 | 38 | 46 | PF03623 | 0.357 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.515 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.410 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.504 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.518 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.568 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.522 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.392 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.318 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.484 |
LIG_FHA_2 | 568 | 574 | PF00498 | 0.593 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.489 |
LIG_LIR_Apic_2 | 466 | 471 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 825 | 831 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 816 | 822 | PF02991 | 0.482 |
LIG_MLH1_MIPbox_1 | 727 | 731 | PF16413 | 0.548 |
LIG_NRBOX | 37 | 43 | PF00104 | 0.407 |
LIG_NRBOX | 71 | 77 | PF00104 | 0.349 |
LIG_NRBOX | 817 | 823 | PF00104 | 0.415 |
LIG_Rb_LxCxE_1 | 263 | 284 | PF01857 | 0.502 |
LIG_SH2_CRK | 468 | 472 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 597 | 601 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.348 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.527 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.574 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.549 |
LIG_Sin3_3 | 664 | 671 | PF02671 | 0.416 |
LIG_SUMO_SIM_anti_2 | 39 | 47 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 830 | 837 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 420 | 425 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 583 | 589 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 647 | 653 | PF11976 | 0.568 |
LIG_TRAF2_1 | 478 | 481 | PF00917 | 0.564 |
LIG_TYR_ITIM | 202 | 207 | PF00017 | 0.420 |
LIG_TYR_ITIM | 489 | 494 | PF00017 | 0.303 |
MOD_CDC14_SPxK_1 | 746 | 749 | PF00782 | 0.515 |
MOD_CDK_SPxK_1 | 743 | 749 | PF00069 | 0.519 |
MOD_CDK_SPxK_1 | 779 | 785 | PF00069 | 0.508 |
MOD_CDK_SPxxK_3 | 779 | 786 | PF00069 | 0.502 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.492 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.573 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.583 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.589 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.601 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.546 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.670 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.589 |
MOD_CK1_1 | 706 | 712 | PF00069 | 0.660 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.535 |
MOD_CK1_1 | 737 | 743 | PF00069 | 0.599 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.744 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.472 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.547 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.402 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.314 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.569 |
MOD_CK2_1 | 810 | 816 | PF00069 | 0.532 |
MOD_Cter_Amidation | 168 | 171 | PF01082 | 0.446 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.402 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.602 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.380 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.592 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.517 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.643 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.552 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.501 |
MOD_GlcNHglycan | 480 | 484 | PF01048 | 0.592 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.684 |
MOD_GlcNHglycan | 561 | 565 | PF01048 | 0.573 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.653 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.574 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.678 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.654 |
MOD_GlcNHglycan | 802 | 805 | PF01048 | 0.597 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.513 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.524 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.429 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.479 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.466 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.492 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.408 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.533 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.580 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.611 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.671 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.719 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.702 |
MOD_GSK3_1 | 722 | 729 | PF00069 | 0.586 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.518 |
MOD_LATS_1 | 524 | 530 | PF00433 | 0.635 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.693 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.497 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.370 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.471 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.526 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.666 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.619 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.446 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.573 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.670 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.533 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.510 |
MOD_NEK2_1 | 822 | 827 | PF00069 | 0.515 |
MOD_NEK2_2 | 640 | 645 | PF00069 | 0.651 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.562 |
MOD_PIKK_1 | 169 | 175 | PF00454 | 0.521 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.477 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.500 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.713 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.691 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.439 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.728 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.536 |
MOD_PIKK_1 | 834 | 840 | PF00454 | 0.584 |
MOD_PK_1 | 548 | 554 | PF00069 | 0.588 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.552 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.396 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.583 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.608 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.636 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.692 |
MOD_PKA_2 | 703 | 709 | PF00069 | 0.552 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.639 |
MOD_PKA_2 | 800 | 806 | PF00069 | 0.540 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.552 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.596 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.481 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.511 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.573 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.506 |
MOD_Plk_4 | 726 | 732 | PF00069 | 0.622 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.665 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.457 |
MOD_ProDKin_1 | 779 | 785 | PF00069 | 0.508 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.502 |
TRG_DiLeu_BaEn_1 | 368 | 373 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.451 |
TRG_DiLeu_BaEn_1 | 669 | 674 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_1 | 841 | 846 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_4 | 841 | 847 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 436 | 441 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 787 | 790 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 796 | 799 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 846 | 848 | PF00400 | 0.488 |
TRG_NLS_MonoExtC_3 | 784 | 789 | PF00514 | 0.527 |
TRG_NLS_MonoExtN_4 | 783 | 790 | PF00514 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 665 | 669 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 77 | 82 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P797 | Leptomonas seymouri | 46% | 100% |
A0A1X0NKL2 | Trypanosomatidae | 26% | 100% |
A0A3R7LZS8 | Trypanosoma rangeli | 27% | 100% |
A0A3S5H829 | Leishmania donovani | 90% | 95% |
A4HPF6 | Leishmania braziliensis | 76% | 100% |
A4ID78 | Leishmania infantum | 89% | 95% |
Q4Q1C9 | Leishmania major | 89% | 100% |
V5B0C2 | Trypanosoma cruzi | 26% | 100% |