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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042555 | MCM complex | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HDE7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006270 | DNA replication initiation | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0007049 | cell cycle | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003688 | DNA replication origin binding | 7 | 12 |
GO:0003690 | double-stranded DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043565 | sequence-specific DNA binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 12 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 704 | 708 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.442 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 785 | 787 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 785 | 787 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 713 | 717 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 749 | 753 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 795 | 799 | PF00082 | 0.530 |
CLV_Separin_Metazoa | 253 | 257 | PF03568 | 0.453 |
DEG_APCC_DBOX_1 | 695 | 703 | PF00400 | 0.478 |
DEG_APCC_DBOX_1 | 794 | 802 | PF00400 | 0.550 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.659 |
DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.539 |
DOC_ANK_TNKS_1 | 26 | 33 | PF00023 | 0.474 |
DOC_CYCLIN_RxL_1 | 111 | 121 | PF00134 | 0.618 |
DOC_CYCLIN_RxL_1 | 633 | 640 | PF00134 | 0.539 |
DOC_CYCLIN_RxL_1 | 94 | 104 | PF00134 | 0.467 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 500 | 509 | PF00134 | 0.374 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 62 | 71 | PF00134 | 0.453 |
DOC_MAPK_DCC_7 | 424 | 434 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 299 | 306 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 480 | 489 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 122 | 130 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 219 | 228 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 404 | 411 | PF00069 | 0.465 |
DOC_PP2B_PxIxI_1 | 674 | 680 | PF00149 | 0.453 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.289 |
DOC_USP7_MATH_2 | 349 | 355 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.514 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.465 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 299 | 306 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 367 | 374 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 512 | 516 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 623 | 630 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 689 | 697 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 748 | 754 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 761 | 769 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 792 | 798 | PF00244 | 0.465 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.482 |
LIG_APCC_ABBAyCdc20_2 | 50 | 56 | PF00400 | 0.408 |
LIG_Clathr_ClatBox_1 | 227 | 231 | PF01394 | 0.465 |
LIG_CtBP_PxDLS_1 | 136 | 140 | PF00389 | 0.278 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.432 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.451 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.437 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.381 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.453 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.453 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.719 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.453 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.453 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.453 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.465 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.450 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.460 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.521 |
LIG_FHA_2 | 729 | 735 | PF00498 | 0.543 |
LIG_HP1_1 | 224 | 228 | PF01393 | 0.514 |
LIG_IBAR_NPY_1 | 223 | 225 | PF08397 | 0.453 |
LIG_Integrin_isoDGR_2 | 25 | 27 | PF01839 | 0.498 |
LIG_Integrin_isoDGR_2 | 578 | 580 | PF01839 | 0.472 |
LIG_Integrin_RGD_1 | 404 | 406 | PF01839 | 0.265 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 544 | 553 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 640 | 649 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 525 | 529 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 544 | 549 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 616 | 621 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 640 | 645 | PF02991 | 0.453 |
LIG_NRP_CendR_1 | 800 | 802 | PF00754 | 0.457 |
LIG_PCNA_PIPBox_1 | 635 | 644 | PF02747 | 0.453 |
LIG_PCNA_yPIPBox_3 | 140 | 151 | PF02747 | 0.453 |
LIG_Pex14_2 | 47 | 51 | PF04695 | 0.453 |
LIG_Pex14_2 | 546 | 550 | PF04695 | 0.453 |
LIG_REV1ctd_RIR_1 | 612 | 621 | PF16727 | 0.295 |
LIG_RPA_C_Fungi | 507 | 519 | PF08784 | 0.306 |
LIG_RPA_C_Fungi | 700 | 712 | PF08784 | 0.322 |
LIG_RPA_C_Fungi | 756 | 768 | PF08784 | 0.452 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.322 |
LIG_SH2_CRK | 781 | 785 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.340 |
LIG_SH2_PTP2 | 225 | 228 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 642 | 645 | PF00017 | 0.322 |
LIG_SH2_PTP2 | 73 | 76 | PF00017 | 0.335 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 234 | 237 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.426 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.391 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.306 |
LIG_SUMO_SIM_par_1 | 258 | 263 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.306 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.432 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.542 |
LIG_TRFH_1 | 225 | 229 | PF08558 | 0.322 |
LIG_TYR_ITIM | 71 | 76 | PF00017 | 0.335 |
LIG_UBA3_1 | 376 | 384 | PF00899 | 0.306 |
MOD_CDK_SPxxK_3 | 268 | 275 | PF00069 | 0.306 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.481 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.373 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.188 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.306 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.597 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.306 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.306 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.306 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.719 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.453 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.381 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.200 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.306 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.676 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.426 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.494 |
MOD_Cter_Amidation | 578 | 581 | PF01082 | 0.717 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.309 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.714 |
MOD_GlcNHglycan | 197 | 201 | PF01048 | 0.453 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.369 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.336 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.404 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.364 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.306 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.306 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.540 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.568 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.611 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.678 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.336 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.299 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.385 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.492 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.228 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.536 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.728 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.306 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.369 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.602 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.522 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.364 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.720 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.306 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.301 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.306 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.322 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.638 |
MOD_GSK3_1 | 613 | 620 | PF00069 | 0.308 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.332 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.266 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.517 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.256 |
MOD_LATS_1 | 759 | 765 | PF00433 | 0.499 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.509 |
MOD_N-GLC_1 | 503 | 508 | PF02516 | 0.306 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.424 |
MOD_N-GLC_1 | 659 | 664 | PF02516 | 0.452 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.439 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.414 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.322 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.306 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.306 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.294 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.612 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.362 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.286 |
MOD_NEK2_2 | 622 | 627 | PF00069 | 0.391 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.584 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.322 |
MOD_PKA_1 | 395 | 401 | PF00069 | 0.200 |
MOD_PKA_1 | 749 | 755 | PF00069 | 0.333 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.449 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.581 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.584 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.655 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.200 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.306 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.306 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.306 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.333 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.555 |
MOD_PKB_1 | 395 | 403 | PF00069 | 0.363 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.534 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.391 |
MOD_Plk_1 | 503 | 509 | PF00069 | 0.306 |
MOD_Plk_1 | 728 | 734 | PF00069 | 0.404 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.318 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.306 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.306 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.306 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.306 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.296 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.302 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.306 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.322 |
MOD_SUMO_for_1 | 784 | 787 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 109 | 117 | PF00179 | 0.322 |
MOD_SUMO_rev_2 | 380 | 385 | PF00179 | 0.340 |
TRG_DiLeu_BaEn_1 | 758 | 763 | PF01217 | 0.414 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.543 |
TRG_DiLeu_LyEn_5 | 758 | 763 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 781 | 784 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 645 | 647 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 696 | 699 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 747 | 750 | PF00400 | 0.425 |
TRG_NES_CRM1_1 | 633 | 648 | PF08389 | 0.322 |
TRG_NLS_Bipartite_1 | 383 | 399 | PF00514 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.306 |
TRG_Pf-PMV_PEXEL_1 | 41 | 46 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 761 | 765 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P686 | Leptomonas seymouri | 35% | 93% |
A0A0N0P860 | Leptomonas seymouri | 31% | 81% |
A0A0N1I2J6 | Leptomonas seymouri | 29% | 90% |
A0A0N1I371 | Leptomonas seymouri | 30% | 100% |
A0A0N1I383 | Leptomonas seymouri | 32% | 78% |
A0A0N1PC47 | Leptomonas seymouri | 88% | 100% |
A0A0S4IVB8 | Bodo saltans | 29% | 92% |
A0A0S4IW18 | Bodo saltans | 30% | 100% |
A0A0S4IYQ3 | Bodo saltans | 61% | 100% |
A0A0S4J5X8 | Bodo saltans | 29% | 100% |
A0A1X0NNF6 | Trypanosomatidae | 30% | 88% |
A0A1X0NQM5 | Trypanosomatidae | 30% | 90% |
A0A1X0NT66 | Trypanosomatidae | 30% | 100% |
A0A1X0NVE7 | Trypanosomatidae | 73% | 100% |
A0A1X0NZT6 | Trypanosomatidae | 31% | 85% |
A0A1X0P1Q1 | Trypanosomatidae | 27% | 100% |
A0A3Q8IAX4 | Leishmania donovani | 31% | 83% |
A0A3R7NBN0 | Trypanosoma rangeli | 30% | 84% |
A0A3S5H7J9 | Leishmania donovani | 29% | 91% |
A0A3S5H7S8 | Leishmania donovani | 30% | 100% |
A0A3S7WQI8 | Leishmania donovani | 30% | 90% |
A0A3S7WY81 | Leishmania donovani | 93% | 100% |
A0A422N694 | Trypanosoma rangeli | 30% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 31% | 92% |
A0A422NDR0 | Trypanosoma rangeli | 27% | 100% |
A0A422NHH5 | Trypanosoma rangeli | 71% | 100% |
A0A422NZW3 | Trypanosoma rangeli | 30% | 100% |
A4FUD9 | Bos taurus | 33% | 99% |
A4HGC9 | Leishmania braziliensis | 31% | 83% |
A4HGU2 | Leishmania braziliensis | 29% | 91% |
A4HKT9 | Leishmania braziliensis | 30% | 100% |
A4HNF5 | Leishmania braziliensis | 26% | 88% |
A4HTX2 | Leishmania infantum | 29% | 90% |
A4I0T0 | Leishmania infantum | 93% | 100% |
A4I3G2 | Leishmania infantum | 31% | 83% |
A4I3W9 | Leishmania infantum | 29% | 91% |
A4I8B8 | Leishmania infantum | 30% | 100% |
B8AEH3 | Oryza sativa subsp. indica | 41% | 100% |
B8AZ14 | Oryza sativa subsp. indica | 32% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 33% | 100% |
B8AZX3 | Oryza sativa subsp. indica | 31% | 97% |
B8B406 | Oryza sativa subsp. indica | 29% | 100% |
B8BKI8 | Oryza sativa subsp. indica | 31% | 83% |
B8BMI1 | Oryza sativa subsp. indica | 31% | 100% |
B9FKM7 | Oryza sativa subsp. japonica | 32% | 100% |
C9ZYH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A4I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A759 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 85% |
D0A936 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 92% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 96% |
D0AAI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D3ZVK1 | Rattus norvegicus | 31% | 97% |
E1BPX4 | Bos taurus | 30% | 98% |
E9AFW6 | Leishmania major | 26% | 100% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 90% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 83% |
E9B059 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
F1M5F3 | Rattus norvegicus | 30% | 71% |
F1QDI9 | Danio rerio | 28% | 71% |
F4KAB8 | Arabidopsis thaliana | 32% | 97% |
I0IUP3 | Gallus gallus | 31% | 97% |
I0IUP4 | Gallus gallus | 27% | 69% |
O75001 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
O80786 | Arabidopsis thaliana | 39% | 100% |
P24279 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 83% |
P25205 | Homo sapiens | 33% | 99% |
P25206 | Mus musculus | 32% | 99% |
P29458 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 86% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 92% |
P29496 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 100% |
P30664 | Xenopus laevis | 32% | 93% |
P30665 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 86% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 91% |
P33991 | Homo sapiens | 31% | 93% |
P33992 | Homo sapiens | 39% | 100% |
P33993 | Homo sapiens | 31% | 100% |
P34647 | Caenorhabditis elegans | 31% | 99% |
P38132 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 95% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 97% |
P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P43299 | Arabidopsis thaliana | 31% | 100% |
P49717 | Mus musculus | 31% | 93% |
P49718 | Mus musculus | 38% | 100% |
P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 90% |
P49735 | Drosophila melanogaster | 29% | 90% |
P49736 | Homo sapiens | 29% | 89% |
P49739 | Xenopus laevis | 35% | 99% |
P53091 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 79% |
P55861 | Xenopus laevis | 30% | 91% |
P55862 | Xenopus laevis | 37% | 100% |
P97310 | Mus musculus | 29% | 89% |
P97311 | Mus musculus | 30% | 98% |
Q0DHC4 | Oryza sativa subsp. japonica | 33% | 100% |
Q0V8B7 | Bos taurus | 39% | 100% |
Q0V9Q6 | Xenopus tropicalis | 30% | 95% |
Q0WVF5 | Arabidopsis thaliana | 32% | 95% |
Q14566 | Homo sapiens | 29% | 98% |
Q21902 | Caenorhabditis elegans | 38% | 100% |
Q24849 | Entamoeba histolytica | 31% | 100% |
Q26454 | Drosophila melanogaster | 29% | 93% |
Q28BS0 | Xenopus tropicalis | 33% | 99% |
Q28CM3 | Xenopus tropicalis | 31% | 98% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 29% | 98% |
Q2KHI9 | Mus musculus | 29% | 71% |
Q2KIZ8 | Bos taurus | 30% | 98% |
Q2QNM1 | Oryza sativa subsp. japonica | 31% | 100% |
Q2R482 | Oryza sativa subsp. japonica | 31% | 83% |
Q3ZBH9 | Bos taurus | 31% | 100% |
Q43704 | Zea mays | 33% | 100% |
Q498J7 | Xenopus laevis | 31% | 97% |
Q4Q826 | Leishmania major | 28% | 100% |
Q4Q8I2 | Leishmania major | 30% | 83% |
Q4QAP2 | Leishmania major | 92% | 99% |
Q4QI01 | Leishmania major | 29% | 90% |
Q54CP4 | Dictyostelium discoideum | 40% | 100% |
Q561P5 | Xenopus tropicalis | 37% | 100% |
Q58884 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 24% | 100% |
Q5F310 | Xenopus laevis | 30% | 97% |
Q5FWY4 | Xenopus laevis | 31% | 98% |
Q5JKB0 | Oryza sativa subsp. japonica | 33% | 93% |
Q5R8G6 | Pongo abelii | 33% | 99% |
Q5XK83 | Xenopus laevis | 32% | 93% |
Q5ZMN2 | Gallus gallus | 32% | 99% |
Q61881 | Mus musculus | 31% | 100% |
Q61J08 | Caenorhabditis briggsae | 30% | 99% |
Q69QA6 | Oryza sativa subsp. japonica | 29% | 100% |
Q6DIH3 | Xenopus tropicalis | 30% | 91% |
Q6F353 | Oryza sativa subsp. japonica | 31% | 97% |
Q6GL41 | Xenopus tropicalis | 31% | 93% |
Q6KAJ4 | Oryza sativa subsp. japonica | 41% | 100% |
Q6NX31 | Xenopus tropicalis | 30% | 100% |
Q6P1V8 | Xenopus tropicalis | 30% | 97% |
Q6PCI7 | Xenopus laevis | 37% | 100% |
Q7Q0Q1 | Anopheles gambiae | 30% | 99% |
Q7ZXB1 | Xenopus laevis | 31% | 100% |
Q7ZXZ0 | Xenopus laevis | 33% | 100% |
Q7ZY18 | Xenopus laevis | 30% | 97% |
Q86B14 | Dictyostelium discoideum | 32% | 93% |
Q91876 | Xenopus laevis | 30% | 100% |
Q95XQ8 | Caenorhabditis elegans | 30% | 97% |
Q9CWV1 | Mus musculus | 31% | 96% |
Q9FL33 | Arabidopsis thaliana | 31% | 100% |
Q9LPD9 | Arabidopsis thaliana | 30% | 86% |
Q9SF37 | Arabidopsis thaliana | 30% | 100% |
Q9SX03 | Zea mays | 33% | 100% |
Q9SX04 | Zea mays | 33% | 100% |
Q9U1E0 | Leishmania major | 30% | 100% |
Q9UJA3 | Homo sapiens | 30% | 95% |
Q9UXG1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 32% | 100% |
Q9V461 | Drosophila melanogaster | 29% | 98% |
Q9VF30 | Drosophila melanogaster | 23% | 91% |
Q9VGW6 | Drosophila melanogaster | 39% | 100% |
Q9XYU0 | Drosophila melanogaster | 30% | 100% |
Q9XYU1 | Drosophila melanogaster | 35% | 98% |
V5B8T3 | Trypanosoma cruzi | 26% | 100% |
V5BGQ5 | Trypanosoma cruzi | 28% | 94% |
V5BHZ8 | Trypanosoma cruzi | 31% | 100% |
V5BQA9 | Trypanosoma cruzi | 31% | 100% |
V5BSG2 | Trypanosoma cruzi | 31% | 92% |
V5C0K6 | Trypanosoma cruzi | 71% | 100% |