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:0005634 | nucleus | 5 | 2 |
GO:0030896 | checkpoint clamp complex | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
Related structures:
AlphaFold database: Q4QF86
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 7 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 2 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 2 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009314 | response to radiation | 3 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010212 | response to ionizing radiation | 4 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 7 |
GO:0010948 | negative regulation of cell cycle process | 6 | 7 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 7 |
GO:0031573 | mitotic intra-S DNA damage checkpoint signaling | 7 | 2 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 2 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 2 |
GO:0045786 | negative regulation of cell cycle | 5 | 7 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
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:0051716 | cellular response to stimulus | 2 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 2 |
GO:0071478 | cellular response to radiation | 4 | 2 |
GO:0071479 | cellular response to ionizing radiation | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0104004 | cellular response to environmental stimulus | 3 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 7 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 7 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.667 |
CLV_C14_Caspase3-7 | 797 | 801 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 726 | 728 | PF00675 | 0.734 |
CLV_PCSK_FUR_1 | 64 | 68 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 519 | 521 | PF00082 | 0.536 |
CLV_PCSK_PC7_1 | 59 | 65 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.793 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.578 |
DEG_APCC_DBOX_1 | 115 | 123 | PF00400 | 0.460 |
DEG_Kelch_Keap1_1 | 634 | 639 | PF01344 | 0.763 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.450 |
DEG_SCF_FBW7_1 | 602 | 608 | PF00400 | 0.710 |
DEG_SCF_FBW7_1 | 763 | 770 | PF00400 | 0.699 |
DEG_SPOP_SBC_1 | 347 | 351 | PF00917 | 0.656 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.695 |
DOC_CKS1_1 | 602 | 607 | PF01111 | 0.708 |
DOC_CKS1_1 | 691 | 696 | PF01111 | 0.726 |
DOC_CYCLIN_yCln2_LP_2 | 65 | 71 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 83 | 91 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 150 | 158 | PF00069 | 0.479 |
DOC_MAPK_RevD_3 | 507 | 521 | PF00069 | 0.543 |
DOC_PP1_RVXF_1 | 726 | 733 | PF00149 | 0.727 |
DOC_PP2B_LxvP_1 | 168 | 171 | PF13499 | 0.627 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.608 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.721 |
DOC_PP2B_PxIxI_1 | 112 | 118 | PF00149 | 0.590 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.531 |
DOC_SPAK_OSR1_1 | 305 | 309 | PF12202 | 0.549 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 742 | 746 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 755 | 759 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 771 | 775 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 812 | 816 | PF00917 | 0.529 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.833 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 696 | 701 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 709 | 714 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 759 | 764 | PF00397 | 0.803 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 520 | 529 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 606 | 614 | PF00244 | 0.840 |
LIG_14-3-3_CanoR_1 | 727 | 731 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 785 | 793 | PF00244 | 0.566 |
LIG_APCC_ABBA_1 | 90 | 95 | PF00400 | 0.513 |
LIG_BIR_III_4 | 411 | 415 | PF00653 | 0.731 |
LIG_BIR_III_4 | 719 | 723 | PF00653 | 0.717 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 728 | 732 | PF00533 | 0.727 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.578 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.472 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.599 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.536 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.514 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.531 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.620 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.717 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.568 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.416 |
LIG_FHA_2 | 706 | 712 | PF00498 | 0.714 |
LIG_GBD_Chelix_1 | 488 | 496 | PF00786 | 0.490 |
LIG_LIR_Apic_2 | 689 | 694 | PF02991 | 0.779 |
LIG_LIR_Gen_1 | 295 | 306 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 392 | 403 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 779 | 787 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 295 | 301 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.722 |
LIG_LIR_Nem_3 | 562 | 566 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 779 | 783 | PF02991 | 0.508 |
LIG_MYND_1 | 88 | 92 | PF01753 | 0.509 |
LIG_Pex14_1 | 273 | 277 | PF04695 | 0.464 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.518 |
LIG_PROFILIN_1 | 435 | 441 | PF00235 | 0.560 |
LIG_SH2_CRK | 315 | 319 | PF00017 | 0.469 |
LIG_SH2_CRK | 691 | 695 | PF00017 | 0.718 |
LIG_SH2_NCK_1 | 787 | 791 | PF00017 | 0.634 |
LIG_SH2_STAP1 | 277 | 281 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 787 | 790 | PF00017 | 0.553 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.592 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.752 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.647 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.720 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.707 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.518 |
LIG_SH3_3 | 757 | 763 | PF00018 | 0.696 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.493 |
LIG_SUMO_SIM_anti_2 | 701 | 708 | PF11976 | 0.830 |
LIG_SUMO_SIM_par_1 | 117 | 123 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 701 | 708 | PF11976 | 0.732 |
LIG_TRAF2_1 | 500 | 503 | PF00917 | 0.570 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.446 |
MOD_CDC14_SPxK_1 | 147 | 150 | PF00782 | 0.633 |
MOD_CDC14_SPxK_1 | 447 | 450 | PF00782 | 0.771 |
MOD_CDK_SPK_2 | 444 | 449 | PF00069 | 0.769 |
MOD_CDK_SPK_2 | 601 | 606 | PF00069 | 0.732 |
MOD_CDK_SPK_2 | 690 | 695 | PF00069 | 0.729 |
MOD_CDK_SPxK_1 | 144 | 150 | PF00069 | 0.506 |
MOD_CDK_SPxK_1 | 444 | 450 | PF00069 | 0.772 |
MOD_CDK_SPxK_1 | 48 | 54 | PF00069 | 0.488 |
MOD_CDK_SPxxK_3 | 709 | 716 | PF00069 | 0.718 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.543 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.506 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.740 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.707 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.519 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.772 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.533 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.526 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.766 |
MOD_CK1_1 | 572 | 578 | PF00069 | 0.646 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.831 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.832 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.710 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.721 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.513 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.802 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.619 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.561 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.417 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.828 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.446 |
MOD_CK2_1 | 786 | 792 | PF00069 | 0.720 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.492 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.473 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.718 |
MOD_GlcNHglycan | 178 | 183 | PF01048 | 0.725 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.726 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.529 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.541 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.571 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.469 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.666 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.712 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.685 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.699 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.760 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.633 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.632 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.470 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.711 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.501 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.859 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.753 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.839 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.754 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.782 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.782 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.644 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.687 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.326 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.558 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.729 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.444 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.545 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.495 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.464 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.489 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.523 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.671 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.499 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.673 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.599 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.677 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.720 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.781 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.728 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.706 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.655 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.733 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.715 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.691 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.625 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.548 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.695 |
MOD_GSK3_1 | 763 | 770 | PF00069 | 0.624 |
MOD_GSK3_1 | 806 | 813 | PF00069 | 0.564 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.628 |
MOD_N-GLC_1 | 648 | 653 | PF02516 | 0.759 |
MOD_N-GLC_1 | 683 | 688 | PF02516 | 0.826 |
MOD_N-GLC_2 | 327 | 329 | PF02516 | 0.603 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.477 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.446 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.601 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.491 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.504 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.613 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.629 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.782 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.832 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.555 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.551 |
MOD_NEK2_2 | 771 | 776 | PF00069 | 0.767 |
MOD_PK_1 | 449 | 455 | PF00069 | 0.772 |
MOD_PKA_1 | 449 | 455 | PF00069 | 0.772 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.332 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.736 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.808 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.772 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.822 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.736 |
MOD_PKA_2 | 677 | 683 | PF00069 | 0.751 |
MOD_PKA_2 | 694 | 700 | PF00069 | 0.817 |
MOD_PKA_2 | 726 | 732 | PF00069 | 0.728 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.471 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.593 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.607 |
MOD_Plk_1 | 590 | 596 | PF00069 | 0.810 |
MOD_Plk_1 | 659 | 665 | PF00069 | 0.817 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.831 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.383 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.437 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.463 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.515 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.485 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.561 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.772 |
MOD_Plk_4 | 771 | 777 | PF00069 | 0.765 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.506 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.683 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.718 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.770 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.488 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.519 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.730 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.830 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.725 |
MOD_ProDKin_1 | 709 | 715 | PF00069 | 0.501 |
MOD_ProDKin_1 | 759 | 765 | PF00069 | 0.803 |
TRG_DiLeu_BaEn_2 | 801 | 807 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_3 | 502 | 508 | PF01217 | 0.526 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 612 | 617 | PF00026 | 0.767 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I126 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IIS7 | Leishmania donovani | 90% | 100% |
A4H871 | Leishmania braziliensis | 73% | 100% |
A4HWJ6 | Leishmania infantum | 86% | 95% |
E9AQ97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |