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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030870 | Mre11 complex | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0140513 | nuclear protein-containing complex | 2 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AKQ6
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 8 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006302 | double-strand break repair | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 8 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 8 |
GO:0007165 | signal transduction | 2 | 8 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 8 |
GO:0010564 | regulation of cell cycle process | 5 | 8 |
GO:0010948 | negative regulation of cell cycle process | 6 | 8 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 8 |
GO:0022402 | cell cycle process | 2 | 8 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0035556 | intracellular signal transduction | 3 | 8 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 8 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 8 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 8 |
GO:0045786 | negative regulation of cell cycle | 5 | 8 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0048519 | negative regulation of biological process | 3 | 8 |
GO:0048523 | negative regulation of cellular process | 4 | 8 |
GO:0050789 | regulation of biological process | 2 | 8 |
GO:0050794 | regulation of cellular process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0051726 | regulation of cell cycle | 4 | 8 |
GO:0065007 | biological regulation | 1 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 8 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 8 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 8 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 8 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 8 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 8 |
GO:1903047 | mitotic cell cycle process | 3 | 8 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003684 | damaged DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 610 | 614 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.419 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 766 | 768 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 772 | 774 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.553 |
CLV_PCSK_FUR_1 | 706 | 710 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 708 | 710 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 765 | 767 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 803 | 805 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.702 |
CLV_PCSK_PC7_1 | 799 | 805 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 683 | 687 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.529 |
DEG_APCC_DBOX_1 | 347 | 355 | PF00400 | 0.413 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.462 |
DEG_COP1_1 | 714 | 723 | PF00400 | 0.620 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.310 |
DEG_SCF_FBW7_1 | 254 | 261 | PF00400 | 0.631 |
DEG_SPOP_SBC_1 | 377 | 381 | PF00917 | 0.469 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.522 |
DOC_CKS1_1 | 314 | 319 | PF01111 | 0.376 |
DOC_CYCLIN_RxL_1 | 405 | 416 | PF00134 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 449 | 455 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 649 | 655 | PF00134 | 0.574 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 282 | 292 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 473 | 481 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 326 | 333 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 39 | 48 | PF00069 | 0.365 |
DOC_PP1_RVXF_1 | 182 | 188 | PF00149 | 0.331 |
DOC_PP1_RVXF_1 | 436 | 442 | PF00149 | 0.438 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.436 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.478 |
DOC_PP4_FxxP_1 | 618 | 621 | PF00568 | 0.660 |
DOC_PP4_FxxP_1 | 661 | 664 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 836 | 840 | PF00917 | 0.557 |
DOC_USP7_UBL2_3 | 686 | 690 | PF12436 | 0.553 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 784 | 789 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.738 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 447 | 452 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 454 | 464 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 498 | 504 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 574 | 582 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 672 | 679 | PF00244 | 0.472 |
LIG_Actin_WH2_2 | 169 | 186 | PF00022 | 0.419 |
LIG_APCC_ABBA_1 | 3 | 8 | PF00400 | 0.366 |
LIG_APCC_ABBA_1 | 478 | 483 | PF00400 | 0.404 |
LIG_BIR_III_2 | 577 | 581 | PF00653 | 0.645 |
LIG_BRCT_BRCA1_1 | 748 | 752 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 838 | 842 | PF00533 | 0.559 |
LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.393 |
LIG_Clathr_ClatBox_1 | 699 | 703 | PF01394 | 0.614 |
LIG_deltaCOP1_diTrp_1 | 613 | 618 | PF00928 | 0.660 |
LIG_EVH1_1 | 521 | 525 | PF00568 | 0.450 |
LIG_EVH1_1 | 655 | 659 | PF00568 | 0.551 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.473 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.513 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.582 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.335 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.330 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.409 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.396 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.550 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.636 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.589 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.423 |
LIG_FHA_1 | 818 | 824 | PF00498 | 0.522 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.483 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.596 |
LIG_FHA_2 | 785 | 791 | PF00498 | 0.508 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.583 |
LIG_Integrin_RGD_1 | 595 | 597 | PF01839 | 0.555 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 337 | 342 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 373 | 378 | PF02991 | 0.484 |
LIG_LIR_Apic_2 | 617 | 621 | PF02991 | 0.621 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 416 | 425 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 535 | 544 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 613 | 622 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 749 | 759 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 839 | 850 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 535 | 539 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 749 | 755 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 839 | 845 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.402 |
LIG_OCRL_FandH_1 | 469 | 481 | PF00620 | 0.417 |
LIG_Pex14_1 | 2 | 6 | PF04695 | 0.312 |
LIG_Pex14_1 | 346 | 350 | PF04695 | 0.425 |
LIG_REV1ctd_RIR_1 | 468 | 477 | PF16727 | 0.430 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.416 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.390 |
LIG_SH2_CRK | 653 | 657 | PF00017 | 0.609 |
LIG_SH2_GRB2like | 431 | 434 | PF00017 | 0.248 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.554 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 653 | 657 | PF00017 | 0.609 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.550 |
LIG_SH2_SRC | 339 | 342 | PF00017 | 0.425 |
LIG_SH2_SRC | 425 | 428 | PF00017 | 0.324 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.406 |
LIG_SH3_1 | 326 | 332 | PF00018 | 0.394 |
LIG_SH3_1 | 519 | 525 | PF00018 | 0.445 |
LIG_SH3_1 | 653 | 659 | PF00018 | 0.611 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.394 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.365 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.481 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.485 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.480 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.604 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.567 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.599 |
LIG_SUMO_SIM_anti_2 | 645 | 650 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 63 | 72 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 697 | 703 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 808 | 817 | PF11976 | 0.644 |
LIG_TRAF2_1 | 535 | 538 | PF00917 | 0.489 |
LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.638 |
LIG_TRAF2_1 | 561 | 564 | PF00917 | 0.624 |
LIG_TRFH_1 | 653 | 657 | PF08558 | 0.609 |
LIG_TYR_ITIM | 506 | 511 | PF00017 | 0.329 |
LIG_WRC_WIRS_1 | 467 | 472 | PF05994 | 0.414 |
MOD_CDK_SPxxK_3 | 784 | 791 | PF00069 | 0.629 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.628 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.581 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.559 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.623 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.416 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.603 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.417 |
MOD_CK1_1 | 632 | 638 | PF00069 | 0.536 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.753 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.616 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.495 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.589 |
MOD_Cter_Amidation | 572 | 575 | PF01082 | 0.681 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.736 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.769 |
MOD_GlcNHglycan | 189 | 193 | PF01048 | 0.348 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.577 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.605 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.552 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.626 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.518 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.420 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.521 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.405 |
MOD_GlcNHglycan | 639 | 642 | PF01048 | 0.600 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.553 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.673 |
MOD_GlcNHglycan | 835 | 839 | PF01048 | 0.586 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.683 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.502 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.582 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.478 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.713 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.350 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.327 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.376 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.614 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.668 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.496 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.528 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.520 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.669 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.404 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.581 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.527 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.757 |
MOD_LATS_1 | 134 | 140 | PF00433 | 0.489 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.252 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.461 |
MOD_N-GLC_1 | 637 | 642 | PF02516 | 0.598 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.500 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.544 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.377 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.413 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.356 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.639 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.519 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.637 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.420 |
MOD_NEK2_1 | 711 | 716 | PF00069 | 0.547 |
MOD_NEK2_2 | 466 | 471 | PF00069 | 0.403 |
MOD_NEK2_2 | 514 | 519 | PF00069 | 0.424 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.576 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.542 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.517 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.706 |
MOD_PKA_1 | 766 | 772 | PF00069 | 0.666 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.460 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.396 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.594 |
MOD_PKA_2 | 671 | 677 | PF00069 | 0.498 |
MOD_PKA_2 | 766 | 772 | PF00069 | 0.666 |
MOD_PKB_1 | 136 | 144 | PF00069 | 0.673 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.378 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.428 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.378 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.377 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.566 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.428 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.269 |
MOD_Plk_2-3 | 86 | 92 | PF00069 | 0.583 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.305 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.396 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.411 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.539 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.447 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.623 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.363 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.390 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.661 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.432 |
MOD_ProDKin_1 | 784 | 790 | PF00069 | 0.593 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.740 |
MOD_SUMO_rev_2 | 632 | 637 | PF00179 | 0.715 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.336 |
TRG_DiLeu_LyEn_5 | 483 | 488 | PF01217 | 0.481 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 605 | 608 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 706 | 709 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 765 | 767 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 803 | 805 | PF00400 | 0.594 |
TRG_NES_CRM1_1 | 410 | 421 | PF08389 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6V8 | Leptomonas seymouri | 46% | 95% |
A0A3S5H5P2 | Leishmania donovani | 88% | 100% |
A0A422NE28 | Trypanosoma rangeli | 30% | 100% |
A4H4J4 | Leishmania braziliensis | 73% | 98% |
A4HSR9 | Leishmania infantum | 88% | 100% |
Q4QJ51 | Leishmania major | 88% | 100% |