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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030870 | Mre11 complex | 3 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0140513 | nuclear protein-containing complex | 2 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H4J4
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 9 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006259 | DNA metabolic process | 4 | 9 |
GO:0006281 | DNA repair | 5 | 9 |
GO:0006302 | double-strand break repair | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0006950 | response to stress | 2 | 9 |
GO:0006974 | DNA damage response | 4 | 9 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 9 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 9 |
GO:0007165 | signal transduction | 2 | 9 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 9 |
GO:0010564 | regulation of cell cycle process | 5 | 9 |
GO:0010948 | negative regulation of cell cycle process | 6 | 9 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 9 |
GO:0022402 | cell cycle process | 2 | 9 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 9 |
GO:0033554 | cellular response to stress | 3 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0035556 | intracellular signal transduction | 3 | 9 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 9 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 9 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 9 |
GO:0045786 | negative regulation of cell cycle | 5 | 9 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0048519 | negative regulation of biological process | 3 | 9 |
GO:0048523 | negative regulation of cellular process | 4 | 9 |
GO:0050789 | regulation of biological process | 2 | 9 |
GO:0050794 | regulation of cellular process | 3 | 9 |
GO:0050896 | response to stimulus | 1 | 9 |
GO:0051716 | cellular response to stimulus | 2 | 9 |
GO:0051726 | regulation of cell cycle | 4 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 9 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 9 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 9 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 9 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 9 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 9 |
GO:1903047 | mitotic cell cycle process | 3 | 9 |
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 | 507 | 511 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 620 | 624 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.438 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 717 | 719 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 781 | 783 | PF00675 | 0.586 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 717 | 719 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 781 | 783 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 700 | 704 | PF00082 | 0.628 |
DEG_APCC_DBOX_1 | 457 | 465 | PF00400 | 0.461 |
DEG_COP1_1 | 723 | 732 | PF00400 | 0.618 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.308 |
DEG_SCF_FBW7_1 | 249 | 256 | PF00400 | 0.591 |
DOC_CDC14_PxL_1 | 332 | 340 | PF14671 | 0.279 |
DOC_CKS1_1 | 250 | 255 | PF01111 | 0.502 |
DOC_CKS1_1 | 309 | 314 | PF01111 | 0.510 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.292 |
DOC_CYCLIN_RxL_1 | 403 | 413 | PF00134 | 0.418 |
DOC_CYCLIN_RxL_1 | 513 | 521 | PF00134 | 0.315 |
DOC_CYCLIN_yCln2_LP_2 | 254 | 260 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 328 | 334 | PF00134 | 0.297 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 470 | 478 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 145 | 152 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 182 | 190 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 321 | 328 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 39 | 48 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 717 | 724 | PF00069 | 0.458 |
DOC_MAPK_NFAT4_5 | 145 | 153 | PF00069 | 0.358 |
DOC_PP1_RVXF_1 | 180 | 186 | PF00149 | 0.365 |
DOC_PP1_RVXF_1 | 433 | 439 | PF00149 | 0.435 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.497 |
DOC_PP2B_PxIxI_1 | 294 | 300 | PF00149 | 0.241 |
DOC_PP4_FxxP_1 | 158 | 161 | PF00568 | 0.329 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.501 |
DOC_PP4_FxxP_1 | 628 | 631 | PF00568 | 0.701 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 813 | 817 | PF00917 | 0.609 |
DOC_USP7_UBL2_3 | 696 | 700 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.270 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.771 |
LIG_14-3-3_CanoR_1 | 145 | 151 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 164 | 168 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 495 | 501 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 572 | 580 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 630 | 635 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 802 | 807 | PF00244 | 0.481 |
LIG_Actin_WH2_2 | 167 | 184 | PF00022 | 0.451 |
LIG_APCC_ABBA_1 | 475 | 480 | PF00400 | 0.438 |
LIG_BIR_III_2 | 575 | 579 | PF00653 | 0.686 |
LIG_BIR_III_4 | 362 | 366 | PF00653 | 0.498 |
LIG_BIR_III_4 | 733 | 737 | PF00653 | 0.493 |
LIG_BRCT_BRCA1_1 | 757 | 761 | PF00533 | 0.548 |
LIG_Clathr_ClatBox_1 | 183 | 187 | PF01394 | 0.424 |
LIG_Clathr_ClatBox_1 | 709 | 713 | PF01394 | 0.644 |
LIG_CtBP_PxDLS_1 | 240 | 246 | PF00389 | 0.453 |
LIG_deltaCOP1_diTrp_1 | 623 | 628 | PF00928 | 0.647 |
LIG_EVH1_1 | 665 | 669 | PF00568 | 0.644 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.456 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.439 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.480 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.316 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.379 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.399 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.535 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.469 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.496 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.688 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.574 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.416 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.476 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.440 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 155 | 161 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.562 |
LIG_LIR_Apic_2 | 373 | 378 | PF02991 | 0.503 |
LIG_LIR_Apic_2 | 611 | 617 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 627 | 631 | PF02991 | 0.686 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 339 | 350 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 413 | 422 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 623 | 632 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 758 | 768 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 842 | 853 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 413 | 417 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 623 | 628 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 758 | 764 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 842 | 848 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.430 |
LIG_MYND_1 | 336 | 340 | PF01753 | 0.314 |
LIG_OCRL_FandH_1 | 466 | 478 | PF00620 | 0.394 |
LIG_Pex14_1 | 2 | 6 | PF04695 | 0.313 |
LIG_Pex14_1 | 341 | 345 | PF04695 | 0.441 |
LIG_REV1ctd_RIR_1 | 465 | 474 | PF16727 | 0.469 |
LIG_SH2_CRK | 282 | 286 | PF00017 | 0.423 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.360 |
LIG_SH2_CRK | 614 | 618 | PF00017 | 0.500 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.645 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 282 | 286 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 663 | 667 | PF00017 | 0.645 |
LIG_SH2_SRC | 121 | 124 | PF00017 | 0.575 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.406 |
LIG_SH2_SRC | 428 | 431 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.379 |
LIG_SH3_1 | 321 | 327 | PF00018 | 0.417 |
LIG_SH3_1 | 334 | 340 | PF00018 | 0.376 |
LIG_SH3_1 | 663 | 669 | PF00018 | 0.646 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.386 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.332 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.426 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.487 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.682 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.685 |
LIG_SH3_3 | 663 | 669 | PF00018 | 0.556 |
LIG_SH3_3 | 791 | 797 | PF00018 | 0.559 |
LIG_SH3_4 | 696 | 703 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 187 | 194 | PF11976 | 0.309 |
LIG_SUMO_SIM_anti_2 | 296 | 301 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 63 | 72 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 707 | 713 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 821 | 830 | PF11976 | 0.654 |
LIG_TRAF2_1 | 532 | 535 | PF00917 | 0.503 |
LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.603 |
LIG_TRFH_1 | 663 | 667 | PF08558 | 0.645 |
LIG_TYR_ITIM | 503 | 508 | PF00017 | 0.330 |
LIG_TYR_ITIM | 603 | 608 | PF00017 | 0.500 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.610 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.541 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.574 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.579 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.405 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.635 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.510 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.561 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.516 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.557 |
MOD_CK1_1 | 723 | 729 | PF00069 | 0.616 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.481 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.619 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.648 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.631 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.747 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.369 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.541 |
MOD_Cter_Amidation | 22 | 25 | PF01082 | 0.280 |
MOD_Cter_Amidation | 570 | 573 | PF01082 | 0.659 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.496 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.692 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.726 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.607 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.660 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.620 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.563 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.703 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.587 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.425 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.530 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.577 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.614 |
MOD_GlcNHglycan | 680 | 684 | PF01048 | 0.563 |
MOD_GlcNHglycan | 757 | 760 | PF01048 | 0.639 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.619 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.563 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.536 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.692 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.519 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.635 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.695 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.422 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.307 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.471 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.580 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.632 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.545 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.554 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.522 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.426 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.563 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.693 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.745 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.454 |
MOD_N-GLC_1 | 802 | 807 | PF02516 | 0.481 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.525 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.526 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.397 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.411 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.413 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.435 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.589 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.503 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.446 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.383 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.623 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.539 |
MOD_NEK2_2 | 511 | 516 | PF00069 | 0.406 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.620 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.565 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.508 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.738 |
MOD_PKA_1 | 775 | 781 | PF00069 | 0.630 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.450 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.605 |
MOD_PKA_2 | 775 | 781 | PF00069 | 0.630 |
MOD_PKB_1 | 133 | 141 | PF00069 | 0.682 |
MOD_PKB_1 | 800 | 808 | PF00069 | 0.477 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.409 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.378 |
MOD_Plk_1 | 609 | 615 | PF00069 | 0.768 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.453 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.479 |
MOD_Plk_2-3 | 504 | 510 | PF00069 | 0.374 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.301 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.350 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.428 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.407 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.516 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.461 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.633 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.325 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.456 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.619 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.393 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.414 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.266 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.630 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.430 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.773 |
TRG_DiLeu_BaEn_1 | 504 | 509 | PF01217 | 0.364 |
TRG_DiLeu_LyEn_5 | 480 | 485 | PF01217 | 0.523 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 668 | 671 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 614 | 616 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 774 | 776 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 810 | 813 | PF00400 | 0.555 |
TRG_NES_CRM1_1 | 460 | 472 | PF08389 | 0.297 |
TRG_NLS_MonoExtC_3 | 132 | 137 | PF00514 | 0.614 |
TRG_NLS_MonoExtN_4 | 133 | 138 | PF00514 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.279 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6V8 | Leptomonas seymouri | 46% | 95% |
A0A0S4JDA4 | Bodo saltans | 28% | 100% |
A0A3S5H5P2 | Leishmania donovani | 73% | 100% |
A4HSR9 | Leishmania infantum | 73% | 100% |
E9AKQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QJ51 | Leishmania major | 73% | 98% |
V5B5S6 | Trypanosoma cruzi | 29% | 100% |