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:0030896 | checkpoint clamp complex | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HWJ6
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 7 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0007165 | signal transduction | 2 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010564 | regulation of cell cycle process | 5 | 7 |
GO:0010948 | negative regulation of cell cycle process | 6 | 7 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 7 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 7 |
GO:0045786 | negative regulation of cell cycle | 5 | 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:0051716 | cellular response to stimulus | 2 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 7 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 7 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0010212 | response to ionizing radiation | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031573 | mitotic intra-S DNA damage checkpoint signaling | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071478 | cellular response to radiation | 4 | 1 |
GO:0071479 | cellular response to ionizing radiation | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 448 | 452 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 723 | 727 | PF00656 | 0.628 |
CLV_C14_Caspase3-7 | 837 | 841 | PF00656 | 0.604 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 559 | 561 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 733 | 735 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.717 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 558 | 560 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 733 | 735 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 558 | 560 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.809 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.744 |
CLV_PCSK_SKI1_1 | 844 | 848 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.699 |
DEG_APCC_DBOX_1 | 156 | 164 | PF00400 | 0.454 |
DEG_Kelch_Keap1_1 | 672 | 677 | PF01344 | 0.738 |
DEG_SCF_FBW7_1 | 640 | 646 | PF00400 | 0.641 |
DEG_SCF_FBW7_1 | 799 | 806 | PF00400 | 0.669 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.451 |
DOC_CKS1_1 | 467 | 472 | PF01111 | 0.699 |
DOC_CKS1_1 | 640 | 645 | PF01111 | 0.645 |
DOC_CKS1_1 | 729 | 734 | PF01111 | 0.707 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 141 | 149 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 141 | 149 | PF00069 | 0.316 |
DOC_MAPK_MEF2A_6 | 191 | 199 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 44 | 53 | PF00069 | 0.463 |
DOC_MAPK_RevD_3 | 546 | 560 | PF00069 | 0.542 |
DOC_PP1_RVXF_1 | 764 | 771 | PF00149 | 0.716 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 373 | 376 | PF13499 | 0.601 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.684 |
DOC_PP2B_PxIxI_1 | 153 | 159 | PF00149 | 0.583 |
DOC_SPAK_OSR1_1 | 347 | 351 | PF12202 | 0.545 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 807 | 811 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 852 | 856 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.479 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 728 | 733 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 747 | 752 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 799 | 804 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 144 | 148 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 157 | 163 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 488 | 493 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 644 | 652 | PF00244 | 0.798 |
LIG_14-3-3_CanoR_1 | 733 | 739 | PF00244 | 0.771 |
LIG_14-3-3_CanoR_1 | 765 | 769 | PF00244 | 0.765 |
LIG_APCC_ABBA_1 | 131 | 136 | PF00400 | 0.450 |
LIG_BIR_III_4 | 451 | 455 | PF00653 | 0.718 |
LIG_BIR_III_4 | 757 | 761 | PF00653 | 0.687 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 766 | 770 | PF00533 | 0.715 |
LIG_DLG_GKlike_1 | 734 | 741 | PF00625 | 0.502 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.487 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.485 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.592 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.532 |
LIG_FHA_1 | 733 | 739 | PF00498 | 0.543 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.565 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.522 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.592 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.697 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.556 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.423 |
LIG_FHA_2 | 744 | 750 | PF00498 | 0.669 |
LIG_GBD_Chelix_1 | 527 | 535 | PF00786 | 0.480 |
LIG_LIR_Apic_2 | 726 | 732 | PF02991 | 0.750 |
LIG_LIR_Gen_1 | 201 | 212 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 337 | 348 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 432 | 441 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 596 | 606 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 815 | 823 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 596 | 601 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 76 | 80 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 815 | 819 | PF02991 | 0.555 |
LIG_MYND_1 | 129 | 133 | PF01753 | 0.471 |
LIG_Pex14_1 | 315 | 319 | PF04695 | 0.464 |
LIG_Pex14_2 | 431 | 435 | PF04695 | 0.509 |
LIG_REV1ctd_RIR_1 | 438 | 446 | PF16727 | 0.450 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.466 |
LIG_SH2_CRK | 729 | 733 | PF00017 | 0.730 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.484 |
LIG_SH2_NCK_1 | 823 | 827 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 295 | 299 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 823 | 826 | PF00017 | 0.578 |
LIG_SH3_1 | 21 | 27 | PF00018 | 0.478 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.492 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.583 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.478 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.744 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.644 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.709 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.667 |
LIG_SH3_3 | 777 | 783 | PF00018 | 0.720 |
LIG_SUMO_SIM_anti_2 | 739 | 746 | PF11976 | 0.775 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 207 | 213 | PF11976 | 0.540 |
LIG_SUMO_SIM_par_1 | 541 | 550 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 739 | 746 | PF11976 | 0.677 |
LIG_TRAF2_1 | 539 | 542 | PF00917 | 0.559 |
LIG_TRAF2_1 | 552 | 555 | PF00917 | 0.441 |
LIG_TRAF2_1 | 833 | 836 | PF00917 | 0.678 |
LIG_WRC_WIRS_1 | 598 | 603 | PF05994 | 0.462 |
MOD_CDC14_SPxK_1 | 188 | 191 | PF00782 | 0.621 |
MOD_CDC14_SPxK_1 | 486 | 489 | PF00782 | 0.752 |
MOD_CDK_SPK_2 | 483 | 488 | PF00069 | 0.746 |
MOD_CDK_SPK_2 | 639 | 644 | PF00069 | 0.675 |
MOD_CDK_SPK_2 | 728 | 733 | PF00069 | 0.706 |
MOD_CDK_SPxK_1 | 185 | 191 | PF00069 | 0.496 |
MOD_CDK_SPxK_1 | 483 | 489 | PF00069 | 0.747 |
MOD_CDK_SPxK_1 | 728 | 734 | PF00069 | 0.595 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.465 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.540 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.496 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.717 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.714 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.511 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.739 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.520 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.657 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.732 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.625 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.643 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.620 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.831 |
MOD_CK1_1 | 685 | 691 | PF00069 | 0.819 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.685 |
MOD_CK1_1 | 718 | 724 | PF00069 | 0.689 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.482 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.507 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.771 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.552 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.546 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.424 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.802 |
MOD_CK2_1 | 734 | 740 | PF00069 | 0.698 |
MOD_CK2_1 | 822 | 828 | PF00069 | 0.693 |
MOD_DYRK1A_RPxSP_1 | 443 | 447 | PF00069 | 0.515 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.456 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.432 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.454 |
MOD_GlcNHglycan | 183 | 187 | PF01048 | 0.463 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.662 |
MOD_GlcNHglycan | 219 | 224 | PF01048 | 0.676 |
MOD_GlcNHglycan | 236 | 241 | PF01048 | 0.685 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.699 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.486 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.472 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.607 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.682 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.646 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.684 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.671 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.676 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.616 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.723 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.617 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.596 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.718 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.500 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.475 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.698 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.487 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.831 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.726 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.484 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.531 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.818 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.743 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.745 |
MOD_GlcNHglycan | 824 | 827 | PF01048 | 0.620 |
MOD_GlcNHglycan | 94 | 98 | PF01048 | 0.480 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.342 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.729 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.420 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.492 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.539 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.465 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.458 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.392 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.514 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.666 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.562 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.541 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.660 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.706 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.374 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.755 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.699 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.566 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.724 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.684 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.817 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.691 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.459 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.739 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.648 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.500 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.717 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.464 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.674 |
MOD_GSK3_1 | 803 | 810 | PF00069 | 0.694 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.548 |
MOD_LATS_1 | 63 | 69 | PF00433 | 0.454 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.670 |
MOD_N-GLC_1 | 686 | 691 | PF02516 | 0.743 |
MOD_N-GLC_1 | 721 | 726 | PF02516 | 0.796 |
MOD_N-GLC_2 | 369 | 371 | PF02516 | 0.601 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.466 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.556 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.475 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.585 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.487 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.607 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.756 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.789 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.776 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.484 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.562 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.544 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.632 |
MOD_NEK2_2 | 807 | 812 | PF00069 | 0.737 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.485 |
MOD_PK_1 | 488 | 494 | PF00069 | 0.743 |
MOD_PKA_1 | 488 | 494 | PF00069 | 0.743 |
MOD_PKA_1 | 559 | 565 | PF00069 | 0.504 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.316 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.631 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.511 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.785 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.743 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.604 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.816 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.456 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.675 |
MOD_PKA_2 | 715 | 721 | PF00069 | 0.712 |
MOD_PKA_2 | 732 | 738 | PF00069 | 0.799 |
MOD_PKA_2 | 764 | 770 | PF00069 | 0.715 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.462 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.601 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.535 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.384 |
MOD_Plk_1 | 628 | 634 | PF00069 | 0.807 |
MOD_Plk_1 | 697 | 703 | PF00069 | 0.794 |
MOD_Plk_1 | 721 | 727 | PF00069 | 0.799 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.438 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.477 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.480 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.509 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.481 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.550 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.743 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.457 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.580 |
MOD_Plk_4 | 807 | 813 | PF00069 | 0.741 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.454 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.666 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.720 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.746 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.514 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.672 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.814 |
MOD_ProDKin_1 | 728 | 734 | PF00069 | 0.707 |
MOD_ProDKin_1 | 747 | 753 | PF00069 | 0.471 |
MOD_ProDKin_1 | 799 | 805 | PF00069 | 0.707 |
MOD_SUMO_rev_2 | 71 | 80 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_2 | 841 | 847 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_3 | 541 | 547 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 487 | 489 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 732 | 734 | PF00400 | 0.591 |
TRG_NLS_MonoExtC_3 | 106 | 111 | PF00514 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 650 | 655 | PF00026 | 0.742 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I126 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IIS7 | Leishmania donovani | 99% | 100% |
A4H871 | Leishmania braziliensis | 73% | 96% |
E9AQ97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4QF86 | Leishmania major | 86% | 100% |