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: E9AWT2
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 | 315 | 319 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 790 | 792 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 784 | 786 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 784 | 786 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 749 | 753 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 794 | 798 | PF00082 | 0.525 |
CLV_Separin_Metazoa | 248 | 252 | PF03568 | 0.453 |
DEG_APCC_DBOX_1 | 694 | 702 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 793 | 801 | PF00400 | 0.545 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.650 |
DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.539 |
DOC_CYCLIN_RxL_1 | 111 | 121 | PF00134 | 0.613 |
DOC_CYCLIN_RxL_1 | 628 | 635 | PF00134 | 0.539 |
DOC_CYCLIN_RxL_1 | 94 | 104 | PF00134 | 0.466 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 62 | 71 | PF00134 | 0.453 |
DOC_MAPK_DCC_7 | 419 | 429 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 214 | 223 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 378 | 386 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 475 | 484 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 122 | 130 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 378 | 386 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 399 | 406 | PF00069 | 0.464 |
DOC_PP2B_PxIxI_1 | 673 | 679 | PF00149 | 0.453 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 721 | 725 | PF00917 | 0.272 |
DOC_USP7_MATH_2 | 344 | 350 | PF00917 | 0.425 |
DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.513 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.464 |
LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 618 | 625 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 760 | 768 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 791 | 797 | PF00244 | 0.461 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.481 |
LIG_Clathr_ClatBox_1 | 222 | 226 | PF01394 | 0.464 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.428 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.450 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.436 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.453 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.453 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.453 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.701 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.453 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.305 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.464 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.459 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.518 |
LIG_HP1_1 | 219 | 223 | PF01393 | 0.513 |
LIG_IBAR_NPY_1 | 218 | 220 | PF08397 | 0.453 |
LIG_Integrin_RGD_1 | 399 | 401 | PF01839 | 0.264 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 635 | 644 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 635 | 640 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.490 |
LIG_NRP_CendR_1 | 799 | 801 | PF00754 | 0.448 |
LIG_PCNA_PIPBox_1 | 630 | 639 | PF02747 | 0.453 |
LIG_PCNA_yPIPBox_3 | 140 | 151 | PF02747 | 0.453 |
LIG_Pex14_2 | 47 | 51 | PF04695 | 0.453 |
LIG_Pex14_2 | 541 | 545 | PF04695 | 0.453 |
LIG_RPA_C_Fungi | 502 | 514 | PF08784 | 0.305 |
LIG_RPA_C_Fungi | 699 | 711 | PF08784 | 0.321 |
LIG_RPA_C_Fungi | 755 | 767 | PF08784 | 0.446 |
LIG_SH2_CRK | 521 | 525 | PF00017 | 0.321 |
LIG_SH2_CRK | 780 | 784 | PF00017 | 0.441 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.340 |
LIG_SH2_NCK_1 | 616 | 620 | PF00017 | 0.297 |
LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.390 |
LIG_SH2_PTP2 | 637 | 640 | PF00017 | 0.321 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 229 | 232 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.425 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.390 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.305 |
LIG_SUMO_SIM_par_1 | 149 | 154 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 253 | 258 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.305 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.432 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.544 |
LIG_TRFH_1 | 220 | 224 | PF08558 | 0.321 |
LIG_UBA3_1 | 371 | 379 | PF00899 | 0.305 |
MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.305 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.476 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.373 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.187 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.305 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.600 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.306 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.305 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.305 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.721 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.452 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.380 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.305 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.425 |
MOD_Cter_Amidation | 574 | 577 | PF01082 | 0.746 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.686 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.308 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.699 |
MOD_GlcNHglycan | 197 | 201 | PF01048 | 0.452 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.335 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.719 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.403 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.305 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.305 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.535 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.589 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.565 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.614 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.679 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.314 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.295 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.384 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.468 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.227 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.529 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.716 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.305 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.596 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.481 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.534 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.704 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.305 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.300 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.305 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.321 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.365 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.639 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.308 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.340 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.265 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.497 |
MOD_LATS_1 | 758 | 764 | PF00433 | 0.493 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.661 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.518 |
MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.305 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.675 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.423 |
MOD_N-GLC_1 | 658 | 663 | PF02516 | 0.451 |
MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.375 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.641 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.438 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.414 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.321 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.305 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.305 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.293 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.607 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.361 |
MOD_NEK2_2 | 617 | 622 | PF00069 | 0.390 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.581 |
MOD_PIKK_1 | 412 | 418 | PF00454 | 0.321 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.413 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.444 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.581 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.658 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.305 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.305 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.305 |
MOD_PKB_1 | 333 | 341 | PF00069 | 0.561 |
MOD_PKB_1 | 390 | 398 | PF00069 | 0.362 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.390 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.305 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.317 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.305 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.305 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.305 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.305 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.295 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.301 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.305 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.321 |
MOD_SUMO_for_1 | 783 | 786 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 109 | 117 | PF00179 | 0.321 |
MOD_SUMO_rev_2 | 375 | 380 | PF00179 | 0.340 |
TRG_DiLeu_BaEn_1 | 757 | 762 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.544 |
TRG_DiLeu_LyEn_5 | 757 | 762 | PF01217 | 0.423 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 695 | 698 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 746 | 749 | PF00400 | 0.418 |
TRG_NES_CRM1_1 | 628 | 643 | PF08389 | 0.321 |
TRG_NLS_Bipartite_1 | 378 | 394 | PF00514 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 41 | 46 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 760 | 764 | PF00026 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P686 | Leptomonas seymouri | 34% | 93% |
A0A0N0P860 | Leptomonas seymouri | 30% | 81% |
A0A0N0P9H0 | Leptomonas seymouri | 28% | 87% |
A0A0N1I2J6 | Leptomonas seymouri | 28% | 90% |
A0A0N1I371 | Leptomonas seymouri | 31% | 100% |
A0A0N1I383 | Leptomonas seymouri | 31% | 78% |
A0A0N1PC47 | Leptomonas seymouri | 88% | 100% |
A0A0S4IVB8 | Bodo saltans | 30% | 92% |
A0A0S4IW18 | Bodo saltans | 31% | 99% |
A0A0S4IYQ3 | Bodo saltans | 60% | 100% |
A0A0S4J5X8 | Bodo saltans | 29% | 100% |
A0A1X0NNF6 | Trypanosomatidae | 31% | 88% |
A0A1X0NQM5 | Trypanosomatidae | 30% | 90% |
A0A1X0NT66 | Trypanosomatidae | 30% | 100% |
A0A1X0NVE7 | Trypanosomatidae | 72% | 100% |
A0A1X0NZT6 | Trypanosomatidae | 31% | 85% |
A0A1X0P1Q1 | Trypanosomatidae | 27% | 100% |
A0A1X0P4W1 | Trypanosomatidae | 27% | 100% |
A0A3Q8IAX4 | Leishmania donovani | 30% | 82% |
A0A3R7MUG3 | Trypanosoma rangeli | 28% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 31% | 84% |
A0A3S5H7J9 | Leishmania donovani | 30% | 91% |
A0A3S5H7S8 | Leishmania donovani | 31% | 100% |
A0A3S7WQI8 | Leishmania donovani | 30% | 89% |
A0A3S7WY81 | Leishmania donovani | 98% | 100% |
A0A3S7X726 | Leishmania donovani | 33% | 91% |
A0A422N694 | Trypanosoma rangeli | 30% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 31% | 92% |
A0A422NDR0 | Trypanosoma rangeli | 26% | 100% |
A0A422NHH5 | Trypanosoma rangeli | 70% | 100% |
A0A422NZW3 | Trypanosoma rangeli | 30% | 100% |
A4FUD9 | Bos taurus | 33% | 99% |
A4H5K0 | Leishmania braziliensis | 30% | 87% |
A4HDE7 | Leishmania braziliensis | 93% | 100% |
A4HGC9 | Leishmania braziliensis | 30% | 82% |
A4HGU2 | Leishmania braziliensis | 29% | 100% |
A4HKT9 | Leishmania braziliensis | 30% | 100% |
A4HNF5 | Leishmania braziliensis | 26% | 87% |
A4HTX2 | Leishmania infantum | 30% | 89% |
A4I0T0 | Leishmania infantum | 98% | 100% |
A4I3G2 | Leishmania infantum | 30% | 82% |
A4I3W9 | Leishmania infantum | 30% | 91% |
A4I8B8 | Leishmania infantum | 31% | 100% |
A4I9B0 | Leishmania infantum | 33% | 91% |
B8AEH3 | Oryza sativa subsp. indica | 40% | 100% |
B8AZ14 | Oryza sativa subsp. indica | 31% | 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 | 32% | 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) | 28% | 100% |
D0A759 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 84% |
D0A936 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 92% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 96% |
D0AAI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D3ZVK1 | Rattus norvegicus | 31% | 97% |
E1BPX4 | Bos taurus | 31% | 98% |
E9AFW6 | Leishmania major | 27% | 88% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 89% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 82% |
E9B059 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 91% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 92% |
E9B719 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 88% |
F1M5F3 | Rattus norvegicus | 29% | 71% |
F1N2W9 | Bos taurus | 28% | 70% |
F1QDI9 | Danio rerio | 29% | 71% |
F4IFF3 | Arabidopsis thaliana | 28% | 100% |
F4KAB8 | Arabidopsis thaliana | 32% | 96% |
F6RIX4 | Xenopus tropicalis | 29% | 72% |
I0IUP3 | Gallus gallus | 31% | 97% |
I0IUP4 | Gallus gallus | 27% | 69% |
O75001 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
O80786 | Arabidopsis thaliana | 40% | 100% |
P24279 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 82% |
P25205 | Homo sapiens | 33% | 99% |
P25206 | Mus musculus | 33% | 99% |
P29458 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 86% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 92% |
P29496 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 100% |
P30664 | Xenopus laevis | 31% | 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 | 32% | 100% |
P34647 | Caenorhabditis elegans | 30% | 99% |
P38132 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 95% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 97% |
P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P43299 | Arabidopsis thaliana | 32% | 100% |
P49717 | Mus musculus | 31% | 93% |
P49718 | Mus musculus | 39% | 100% |
P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 90% |
P49735 | Drosophila melanogaster | 30% | 90% |
P49736 | Homo sapiens | 30% | 89% |
P49739 | Xenopus laevis | 34% | 99% |
P53091 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 79% |
P55861 | Xenopus laevis | 31% | 90% |
P55862 | Xenopus laevis | 38% | 100% |
P97310 | Mus musculus | 30% | 89% |
P97311 | Mus musculus | 31% | 98% |
Q0DHC4 | Oryza sativa subsp. japonica | 33% | 100% |
Q0V8B7 | Bos taurus | 39% | 100% |
Q0V9Q6 | Xenopus tropicalis | 31% | 95% |
Q0WVF5 | Arabidopsis thaliana | 31% | 95% |
Q14566 | Homo sapiens | 30% | 98% |
Q21902 | Caenorhabditis elegans | 39% | 100% |
Q24849 | Entamoeba histolytica | 30% | 100% |
Q26454 | Drosophila melanogaster | 30% | 92% |
Q28BS0 | Xenopus tropicalis | 34% | 99% |
Q28CM3 | Xenopus tropicalis | 31% | 98% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 32% | 98% |
Q2KHI9 | Mus musculus | 27% | 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% |
Q4Q3R6 | Leishmania major | 34% | 91% |
Q4Q826 | Leishmania major | 29% | 100% |
Q4Q8I2 | Leishmania major | 30% | 83% |
Q4QAP2 | Leishmania major | 98% | 100% |
Q4QI01 | Leishmania major | 30% | 89% |
Q54CP4 | Dictyostelium discoideum | 40% | 100% |
Q561P5 | Xenopus tropicalis | 38% | 100% |
Q58884 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 25% | 100% |
Q5F310 | Xenopus laevis | 29% | 96% |
Q5FWY4 | Xenopus laevis | 31% | 98% |
Q5JKB0 | Oryza sativa subsp. japonica | 32% | 93% |
Q5R8G6 | Pongo abelii | 33% | 99% |
Q5XK83 | Xenopus laevis | 31% | 93% |
Q5ZMN2 | Gallus gallus | 32% | 99% |
Q61881 | Mus musculus | 32% | 100% |
Q61J08 | Caenorhabditis briggsae | 29% | 99% |
Q69QA6 | Oryza sativa subsp. japonica | 29% | 100% |
Q6DIH3 | Xenopus tropicalis | 30% | 91% |
Q6F353 | Oryza sativa subsp. japonica | 32% | 97% |
Q6GL41 | Xenopus tropicalis | 31% | 93% |
Q6KAJ4 | Oryza sativa subsp. japonica | 40% | 100% |
Q6NRM6 | Xenopus laevis | 29% | 70% |
Q6NX31 | Xenopus tropicalis | 29% | 100% |
Q6P1V8 | Xenopus tropicalis | 30% | 97% |
Q6PCI7 | Xenopus laevis | 38% | 100% |
Q7Q0Q1 | Anopheles gambiae | 30% | 98% |
Q7ZXB1 | Xenopus laevis | 30% | 100% |
Q7ZXZ0 | Xenopus laevis | 33% | 99% |
Q7ZY18 | Xenopus laevis | 30% | 97% |
Q86B14 | Dictyostelium discoideum | 31% | 92% |
Q91876 | Xenopus laevis | 30% | 100% |
Q95XQ8 | Caenorhabditis elegans | 31% | 97% |
Q9CWV1 | Mus musculus | 30% | 96% |
Q9FL33 | Arabidopsis thaliana | 31% | 100% |
Q9LPD9 | Arabidopsis thaliana | 31% | 86% |
Q9NXL9 | Homo sapiens | 28% | 70% |
Q9SF37 | Arabidopsis thaliana | 30% | 100% |
Q9SX03 | Zea mays | 33% | 100% |
Q9SX04 | Zea mays | 33% | 100% |
Q9U1E0 | Leishmania major | 30% | 100% |
Q9UJA3 | Homo sapiens | 31% | 95% |
Q9UXG1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 30% | 100% |
Q9V461 | Drosophila melanogaster | 30% | 98% |
Q9VF30 | Drosophila melanogaster | 23% | 91% |
Q9VGW6 | Drosophila melanogaster | 40% | 100% |
Q9XYU0 | Drosophila melanogaster | 31% | 100% |
Q9XYU1 | Drosophila melanogaster | 34% | 98% |
V5B8T3 | Trypanosoma cruzi | 27% | 100% |
V5BGQ5 | Trypanosoma cruzi | 29% | 94% |
V5BQA9 | Trypanosoma cruzi | 31% | 100% |
V5BSG2 | Trypanosoma cruzi | 33% | 92% |
V5C0K6 | Trypanosoma cruzi | 71% | 100% |