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:0005634 | nucleus | 5 | 1 |
GO:0016592 | mediator complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HFW9
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0000086 | G2/M transition of mitotic cell cycle | 5 | 1 |
GO:0000365 | mRNA trans splicing, via spliceosome | 9 | 1 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044839 | cell cycle G2/M phase transition | 4 | 1 |
GO:0045291 | mRNA trans splicing, SL addition | 10 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004693 | cyclin-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0008353 | RNA polymerase II CTD heptapeptide repeat kinase activity | 5 | 1 |
GO:0097472 | cyclin-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 901 | 905 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.647 |
CLV_C14_Caspase3-7 | 931 | 935 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 936 | 940 | PF00656 | 0.626 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 922 | 924 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 922 | 924 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.773 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 759 | 763 | PF00082 | 0.242 |
CLV_Separin_Metazoa | 772 | 776 | PF03568 | 0.413 |
DEG_COP1_1 | 33 | 42 | PF00400 | 0.532 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.648 |
DEG_ODPH_VHL_1 | 907 | 919 | PF01847 | 0.481 |
DEG_SPOP_SBC_1 | 400 | 404 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.605 |
DEG_SPOP_SBC_1 | 528 | 532 | PF00917 | 0.407 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.697 |
DOC_CDC14_PxL_1 | 618 | 626 | PF14671 | 0.291 |
DOC_CYCLIN_RxL_1 | 648 | 658 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 649 | 655 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 578 | 587 | PF00069 | 0.291 |
DOC_MAPK_MEF2A_6 | 352 | 360 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 491 | 499 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 800 | 808 | PF00069 | 0.504 |
DOC_MAPK_RevD_3 | 635 | 651 | PF00069 | 0.385 |
DOC_PP1_RVXF_1 | 563 | 570 | PF00149 | 0.385 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.582 |
DOC_PP2B_LxvP_1 | 670 | 673 | PF13499 | 0.367 |
DOC_PP2B_PxIxI_1 | 803 | 809 | PF00149 | 0.508 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.603 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 717 | 721 | PF00917 | 0.210 |
DOC_USP7_MATH_1 | 820 | 824 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.691 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.422 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 867 | 872 | PF00397 | 0.635 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 279 | 287 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 290 | 297 | PF00244 | 0.345 |
LIG_14-3-3_CanoR_1 | 381 | 386 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 390 | 395 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 696 | 706 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 759 | 767 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 922 | 929 | PF00244 | 0.511 |
LIG_BIR_III_2 | 811 | 815 | PF00653 | 0.580 |
LIG_BIR_III_4 | 58 | 62 | PF00653 | 0.508 |
LIG_Clathr_ClatBox_1 | 371 | 375 | PF01394 | 0.532 |
LIG_deltaCOP1_diTrp_1 | 636 | 644 | PF00928 | 0.367 |
LIG_DLG_GKlike_1 | 390 | 398 | PF00625 | 0.549 |
LIG_EVH1_2 | 80 | 84 | PF00568 | 0.691 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.758 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.724 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.699 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.291 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.367 |
LIG_FHA_1 | 940 | 946 | PF00498 | 0.572 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.544 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.458 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.807 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.718 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.626 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.727 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.501 |
LIG_GBD_Chelix_1 | 111 | 119 | PF00786 | 0.392 |
LIG_LIR_Apic_2 | 616 | 622 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 494 | 504 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 558 | 569 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 589 | 600 | PF02991 | 0.385 |
LIG_LIR_LC3C_4 | 184 | 189 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 675 | 681 | PF02991 | 0.315 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.562 |
LIG_Pex14_2 | 644 | 648 | PF04695 | 0.367 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.417 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.336 |
LIG_SH2_CRK | 561 | 565 | PF00017 | 0.367 |
LIG_SH2_CRK | 682 | 686 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 274 | 278 | PF00017 | 0.472 |
LIG_SH2_PTP2 | 592 | 595 | PF00017 | 0.385 |
LIG_SH2_SRC | 891 | 894 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 513 | 517 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 631 | 635 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 297 | 300 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.357 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.483 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.691 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.428 |
LIG_SH3_CIN85_PxpxPR_1 | 376 | 381 | PF14604 | 0.660 |
LIG_SUMO_SIM_anti_2 | 353 | 358 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 370 | 375 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 613 | 619 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 733 | 740 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 370 | 375 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 662 | 668 | PF11976 | 0.385 |
LIG_TRAF2_1 | 673 | 676 | PF00917 | 0.363 |
LIG_TRAF2_1 | 908 | 911 | PF00917 | 0.496 |
LIG_TYR_ITIM | 559 | 564 | PF00017 | 0.367 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.612 |
MOD_CDC14_SPxK_1 | 385 | 388 | PF00782 | 0.640 |
MOD_CDK_SPK_2 | 537 | 542 | PF00069 | 0.508 |
MOD_CDK_SPxK_1 | 382 | 388 | PF00069 | 0.639 |
MOD_CDK_SPxxK_3 | 374 | 381 | PF00069 | 0.632 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.694 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.674 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.512 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.544 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.698 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.774 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.821 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.550 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.385 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.629 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.577 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.624 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.548 |
MOD_CK1_1 | 865 | 871 | PF00069 | 0.576 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.770 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.631 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.676 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.747 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.612 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.491 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.325 |
MOD_Cter_Amidation | 176 | 179 | PF01082 | 0.545 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.704 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.713 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.652 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.622 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.629 |
MOD_GlcNHglycan | 259 | 263 | PF01048 | 0.400 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.652 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.654 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.615 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.540 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.525 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.340 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.206 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.767 |
MOD_GlcNHglycan | 822 | 825 | PF01048 | 0.802 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.716 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.702 |
MOD_GlcNHglycan | 867 | 870 | PF01048 | 0.645 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.699 |
MOD_GlcNHglycan | 899 | 903 | PF01048 | 0.687 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.447 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.514 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.471 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.619 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.566 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.590 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.676 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.630 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.548 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.669 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.561 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.669 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.684 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.717 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.666 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.704 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.702 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.408 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.706 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.695 |
MOD_GSK3_1 | 874 | 881 | PF00069 | 0.728 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.606 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.688 |
MOD_LATS_1 | 920 | 926 | PF00433 | 0.602 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.681 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.706 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.715 |
MOD_N-GLC_1 | 697 | 702 | PF02516 | 0.454 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.455 |
MOD_N-GLC_2 | 500 | 502 | PF02516 | 0.273 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.412 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.569 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.540 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.645 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.412 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.281 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.319 |
MOD_NEK2_1 | 737 | 742 | PF00069 | 0.367 |
MOD_NEK2_1 | 883 | 888 | PF00069 | 0.683 |
MOD_OFUCOSY | 103 | 108 | PF10250 | 0.565 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.714 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.507 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.477 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.530 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.692 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.362 |
MOD_PIKK_1 | 657 | 663 | PF00454 | 0.210 |
MOD_PIKK_1 | 806 | 812 | PF00454 | 0.674 |
MOD_PK_1 | 555 | 561 | PF00069 | 0.385 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.512 |
MOD_PKA_1 | 381 | 387 | PF00069 | 0.539 |
MOD_PKA_1 | 511 | 517 | PF00069 | 0.329 |
MOD_PKA_1 | 748 | 754 | PF00069 | 0.385 |
MOD_PKA_1 | 922 | 928 | PF00069 | 0.599 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.772 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.692 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.489 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.753 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.594 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.602 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.690 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.335 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.443 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.385 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.291 |
MOD_PKA_2 | 921 | 927 | PF00069 | 0.620 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.589 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.291 |
MOD_Plk_2-3 | 416 | 422 | PF00069 | 0.634 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.486 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.631 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.567 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.532 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.392 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.547 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.405 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.300 |
MOD_Plk_4 | 702 | 708 | PF00069 | 0.341 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.447 |
MOD_Plk_4 | 878 | 884 | PF00069 | 0.552 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.642 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.503 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.622 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.717 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.558 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.627 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.503 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.385 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.601 |
MOD_ProDKin_1 | 867 | 873 | PF00069 | 0.635 |
MOD_SUMO_rev_2 | 518 | 528 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 573 | 583 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_4 | 912 | 918 | PF01217 | 0.601 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 649 | 651 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 746 | 749 | PF00400 | 0.385 |
TRG_NES_CRM1_1 | 661 | 676 | PF08389 | 0.210 |
TRG_NLS_Bipartite_1 | 426 | 446 | PF00514 | 0.677 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.592 |
TRG_NLS_MonoExtC_3 | 441 | 447 | PF00514 | 0.682 |
TRG_NLS_MonoExtN_4 | 440 | 446 | PF00514 | 0.540 |
TRG_NLS_MonoExtN_4 | 9 | 15 | PF00514 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 574 | 579 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 950 | 955 | PF00026 | 0.728 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6G8 | Leptomonas seymouri | 50% | 100% |
A0A3R7KFZ3 | Trypanosoma rangeli | 36% | 100% |
A0A3S5H7I2 | Leishmania donovani | 77% | 100% |
A4I302 | Leishmania infantum | 77% | 100% |
C9ZJF3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ADH4 | Leishmania major | 77% | 99% |
E9AZ98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |