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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0030870 | Mre11 complex | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
Related structures:
AlphaFold database: Q4QJ51
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 7 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 7 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006302 | double-strand break repair | 6 | 7 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 7 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 7 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 7 |
GO:0010564 | regulation of cell cycle process | 5 | 7 |
GO:0010948 | negative regulation of cell cycle process | 6 | 7 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 7 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 7 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 7 |
GO:0032392 | DNA geometric change | 7 | 2 |
GO:0032508 | DNA duplex unwinding | 8 | 2 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 7 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 7 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 7 |
GO:0045786 | negative regulation of cell cycle | 5 | 7 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0048519 | negative regulation of biological process | 3 | 7 |
GO:0048523 | negative regulation of cellular process | 4 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051276 | chromosome organization | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071103 | DNA conformation change | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 7 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 7 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 7 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 7 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 7 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 7 |
GO:1903047 | mitotic cell cycle process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003684 | damaged DNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.347 |
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.388 |
CLV_MEL_PAP_1 | 539 | 545 | PF00089 | 0.352 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 604 | 606 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 765 | 767 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 771 | 773 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.619 |
CLV_PCSK_FUR_1 | 705 | 709 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 764 | 766 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 771 | 773 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 775 | 777 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.672 |
CLV_PCSK_PC7_1 | 771 | 777 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 689 | 693 | PF00082 | 0.562 |
DEG_APCC_DBOX_1 | 347 | 355 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.458 |
DEG_COP1_1 | 713 | 722 | PF00400 | 0.635 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.325 |
DEG_SCF_FBW7_1 | 254 | 261 | PF00400 | 0.655 |
DEG_SCF_FBW7_1 | 375 | 380 | PF00400 | 0.476 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.517 |
DOC_CKS1_1 | 314 | 319 | PF01111 | 0.395 |
DOC_CYCLIN_RxL_1 | 405 | 416 | PF00134 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 449 | 455 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 648 | 654 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 21 | 31 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 282 | 292 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 473 | 481 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 326 | 333 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 39 | 48 | PF00069 | 0.392 |
DOC_PP1_RVXF_1 | 182 | 188 | PF00149 | 0.347 |
DOC_PP1_RVXF_1 | 436 | 442 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.472 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.443 |
DOC_PP2B_LxvP_1 | 692 | 695 | PF13499 | 0.566 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.343 |
DOC_PP4_FxxP_1 | 617 | 620 | PF00568 | 0.665 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 826 | 830 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 839 | 843 | PF00917 | 0.555 |
DOC_USP7_UBL2_3 | 685 | 689 | PF12436 | 0.584 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 783 | 788 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 138 | 148 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 238 | 246 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 498 | 504 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 542 | 550 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 573 | 581 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 619 | 624 | PF00244 | 0.569 |
LIG_Actin_WH2_2 | 169 | 186 | PF00022 | 0.371 |
LIG_APCC_ABBA_1 | 3 | 8 | PF00400 | 0.377 |
LIG_APCC_ABBA_1 | 478 | 483 | PF00400 | 0.351 |
LIG_BIR_III_2 | 576 | 580 | PF00653 | 0.661 |
LIG_BRCT_BRCA1_1 | 747 | 751 | PF00533 | 0.576 |
LIG_BRCT_BRCA1_1 | 841 | 845 | PF00533 | 0.585 |
LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.353 |
LIG_Clathr_ClatBox_1 | 698 | 702 | PF01394 | 0.578 |
LIG_CtBP_PxDLS_1 | 245 | 251 | PF00389 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 612 | 617 | PF00928 | 0.674 |
LIG_EVH1_1 | 521 | 525 | PF00568 | 0.455 |
LIG_EVH1_1 | 654 | 658 | PF00568 | 0.561 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.419 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.475 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.605 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.365 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.406 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.377 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.402 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.444 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.480 |
LIG_FHA_1 | 642 | 648 | PF00498 | 0.550 |
LIG_FHA_1 | 714 | 720 | PF00498 | 0.629 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.435 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.384 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.424 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.574 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.633 |
LIG_LIR_Apic_2 | 157 | 163 | PF02991 | 0.404 |
LIG_LIR_Apic_2 | 337 | 342 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 616 | 620 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 416 | 425 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 535 | 543 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 612 | 621 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 748 | 758 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 842 | 853 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 416 | 420 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 535 | 539 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 612 | 617 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 748 | 754 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 842 | 848 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.423 |
LIG_OCRL_FandH_1 | 469 | 481 | PF00620 | 0.359 |
LIG_Pex14_1 | 2 | 6 | PF04695 | 0.326 |
LIG_Pex14_1 | 346 | 350 | PF04695 | 0.373 |
LIG_REV1ctd_RIR_1 | 468 | 477 | PF16727 | 0.369 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.431 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.336 |
LIG_SH2_CRK | 652 | 656 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 287 | 291 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 652 | 656 | PF00017 | 0.561 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.532 |
LIG_SH2_SRC | 339 | 342 | PF00017 | 0.460 |
LIG_SH2_SRC | 425 | 428 | PF00017 | 0.335 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.352 |
LIG_SH3_1 | 326 | 332 | PF00018 | 0.418 |
LIG_SH3_1 | 519 | 525 | PF00018 | 0.451 |
LIG_SH3_1 | 652 | 658 | PF00018 | 0.562 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.418 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.486 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.451 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.591 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.562 |
LIG_SH3_3 | 691 | 697 | PF00018 | 0.562 |
LIG_SUMO_SIM_anti_2 | 644 | 649 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 63 | 72 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 696 | 703 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 806 | 816 | PF11976 | 0.585 |
LIG_TRAF2_1 | 535 | 538 | PF00917 | 0.432 |
LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.618 |
LIG_TRAF2_1 | 561 | 564 | PF00917 | 0.613 |
LIG_TRFH_1 | 373 | 377 | PF08558 | 0.473 |
LIG_TRFH_1 | 652 | 656 | PF08558 | 0.561 |
LIG_TYR_ITIM | 506 | 511 | PF00017 | 0.339 |
LIG_WRC_WIRS_1 | 467 | 472 | PF05994 | 0.341 |
MOD_CDK_SPxxK_3 | 783 | 790 | PF00069 | 0.630 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.589 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.535 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.507 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.411 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.526 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.408 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.389 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.632 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.643 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.520 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.342 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.432 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.569 |
MOD_Cter_Amidation | 571 | 574 | PF01082 | 0.608 |
MOD_Cter_Amidation | 773 | 776 | PF01082 | 0.551 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.748 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.781 |
MOD_GlcNHglycan | 189 | 193 | PF01048 | 0.363 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.513 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.604 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.600 |
MOD_GlcNHglycan | 242 | 246 | PF01048 | 0.413 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.547 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.585 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.582 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.499 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.428 |
MOD_GlcNHglycan | 442 | 446 | PF01048 | 0.450 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.482 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.357 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.619 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.616 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.585 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.500 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.573 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.616 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.684 |
MOD_GlcNHglycan | 837 | 840 | PF01048 | 0.564 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.513 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.644 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.455 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.560 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.686 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.370 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.394 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.727 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.494 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.460 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.564 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.428 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.565 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.662 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.485 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.647 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.453 |
MOD_N-GLC_1 | 636 | 641 | PF02516 | 0.621 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.409 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.503 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.367 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.381 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.345 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.561 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.485 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.462 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.607 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.373 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.546 |
MOD_NEK2_1 | 822 | 827 | PF00069 | 0.639 |
MOD_NEK2_2 | 466 | 471 | PF00069 | 0.342 |
MOD_NEK2_2 | 514 | 519 | PF00069 | 0.424 |
MOD_NEK2_2 | 638 | 643 | PF00069 | 0.524 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.600 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.586 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.483 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.646 |
MOD_PKA_1 | 765 | 771 | PF00069 | 0.612 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.464 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.487 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.392 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.605 |
MOD_PKA_2 | 597 | 603 | PF00069 | 0.627 |
MOD_PKA_2 | 765 | 771 | PF00069 | 0.612 |
MOD_PKB_1 | 134 | 142 | PF00069 | 0.636 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.367 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.393 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.557 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.381 |
MOD_Plk_1 | 839 | 845 | PF00069 | 0.506 |
MOD_Plk_2-3 | 427 | 433 | PF00069 | 0.339 |
MOD_Plk_2-3 | 507 | 513 | PF00069 | 0.386 |
MOD_Plk_2-3 | 86 | 92 | PF00069 | 0.598 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.514 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.355 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.346 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.451 |
MOD_Plk_4 | 710 | 716 | PF00069 | 0.550 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.649 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.590 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.328 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.497 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.522 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.480 |
MOD_ProDKin_1 | 783 | 789 | PF00069 | 0.591 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.656 |
MOD_SUMO_rev_2 | 631 | 636 | PF00179 | 0.632 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.339 |
TRG_DiLeu_LyEn_5 | 483 | 488 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.572 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 604 | 607 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 705 | 708 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 764 | 766 | PF00400 | 0.638 |
TRG_NES_CRM1_1 | 410 | 421 | PF08389 | 0.324 |
TRG_NLS_MonoExtC_3 | 133 | 138 | PF00514 | 0.661 |
TRG_NLS_MonoExtN_4 | 133 | 139 | PF00514 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6V8 | Leptomonas seymouri | 46% | 95% |
A0A3S5H5P2 | Leishmania donovani | 92% | 100% |
A4H4J4 | Leishmania braziliensis | 73% | 100% |
A4HSR9 | Leishmania infantum | 92% | 100% |
E9AKQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |