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: 15 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: E9B512
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0008380 | RNA splicing | 7 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003676 | nucleic acid binding | 3 | 14 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004386 | helicase activity | 2 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003724 | RNA helicase activity | 3 | 8 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 8 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 603 | 607 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 713 | 717 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 779 | 783 | PF00656 | 0.401 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 790 | 792 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.148 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 790 | 792 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.226 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 627 | 629 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.710 |
CLV_PCSK_PC1ET2_1 | 805 | 807 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 240 | 246 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 679 | 683 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 715 | 719 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 486 | 490 | PF03568 | 0.333 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.373 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.545 |
DEG_SPOP_SBC_1 | 73 | 77 | PF00917 | 0.572 |
DOC_CKS1_1 | 691 | 696 | PF01111 | 0.454 |
DOC_CYCLIN_RxL_1 | 236 | 243 | PF00134 | 0.527 |
DOC_CYCLIN_RxL_1 | 555 | 564 | PF00134 | 0.425 |
DOC_CYCLIN_RxL_1 | 90 | 98 | PF00134 | 0.426 |
DOC_CYCLIN_yCln2_LP_2 | 366 | 372 | PF00134 | 0.459 |
DOC_MAPK_DCC_7 | 545 | 554 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 156 | 163 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 17 | 24 | PF00069 | 0.270 |
DOC_MAPK_gen_1 | 214 | 221 | PF00069 | 0.364 |
DOC_MAPK_gen_1 | 244 | 252 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 368 | 378 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 4 | 12 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 651 | 659 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 66 | 73 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 712 | 722 | PF00069 | 0.425 |
DOC_MAPK_HePTP_8 | 163 | 175 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 116 | 124 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 166 | 175 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 371 | 380 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 652 | 661 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 66 | 73 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 715 | 722 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 657 | 660 | PF13499 | 0.500 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 512 | 515 | PF00568 | 0.341 |
DOC_PP4_FxxP_1 | 585 | 588 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 691 | 694 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 795 | 799 | PF00917 | 0.575 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 469 | 479 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 636 | 641 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 709 | 715 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 724 | 728 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 757 | 766 | PF00244 | 0.429 |
LIG_Actin_WH2_2 | 191 | 207 | PF00022 | 0.415 |
LIG_BIR_III_4 | 604 | 608 | PF00653 | 0.349 |
LIG_BRCT_BRCA1_1 | 472 | 476 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 521 | 525 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 751 | 755 | PF00533 | 0.454 |
LIG_deltaCOP1_diTrp_1 | 763 | 773 | PF00928 | 0.458 |
LIG_eIF4E_1 | 105 | 111 | PF01652 | 0.265 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.312 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.363 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.499 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.447 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.423 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.527 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.688 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.414 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.421 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.394 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.332 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.673 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.500 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.441 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.527 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.499 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.499 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.648 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.369 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.315 |
LIG_FHA_2 | 711 | 717 | PF00498 | 0.421 |
LIG_GBD_Chelix_1 | 233 | 241 | PF00786 | 0.327 |
LIG_LIR_Apic_2 | 282 | 287 | PF02991 | 0.450 |
LIG_LIR_Apic_2 | 440 | 444 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 509 | 515 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 473 | 480 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 523 | 534 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 683 | 694 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 739 | 748 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 771 | 781 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 144 | 149 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 683 | 689 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 708 | 714 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 739 | 743 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 771 | 777 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.397 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.527 |
LIG_PCNA_TLS_4 | 679 | 686 | PF02747 | 0.471 |
LIG_PDZ_Class_3 | 804 | 809 | PF00595 | 0.703 |
LIG_Pex14_2 | 616 | 620 | PF04695 | 0.323 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.460 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.415 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.497 |
LIG_SH2_CRK | 647 | 651 | PF00017 | 0.360 |
LIG_SH2_CRK | 711 | 715 | PF00017 | 0.458 |
LIG_SH2_CRK | 92 | 96 | PF00017 | 0.370 |
LIG_SH2_GRB2like | 631 | 634 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 471 | 475 | PF00017 | 0.204 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.329 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 631 | 635 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 285 | 288 | PF00017 | 0.257 |
LIG_SH2_STAT3 | 427 | 430 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.397 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.383 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.478 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.533 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.336 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.360 |
LIG_SH3_3 | 691 | 697 | PF00018 | 0.479 |
LIG_SH3_5 | 289 | 293 | PF00018 | 0.392 |
LIG_Sin3_3 | 248 | 255 | PF02671 | 0.505 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 354 | 362 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 373 | 379 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 495 | 501 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 120 | 127 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 495 | 501 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 766 | 772 | PF11976 | 0.463 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.493 |
LIG_UBA3_1 | 38 | 42 | PF00899 | 0.553 |
LIG_UBA3_1 | 559 | 565 | PF00899 | 0.416 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.258 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.384 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.258 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.524 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.338 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.354 |
MOD_CK2_1 | 757 | 763 | PF00069 | 0.335 |
MOD_Cter_Amidation | 543 | 546 | PF01082 | 0.358 |
MOD_Cter_Amidation | 625 | 628 | PF01082 | 0.466 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.258 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.258 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.491 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.334 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.571 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.625 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.258 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.388 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.313 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.372 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.570 |
MOD_GlcNHglycan | 796 | 800 | PF01048 | 0.544 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.508 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.396 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.193 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.687 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.303 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.367 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.573 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.422 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.423 |
MOD_LATS_1 | 182 | 188 | PF00433 | 0.358 |
MOD_N-GLC_1 | 718 | 723 | PF02516 | 0.381 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.297 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.534 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.409 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.319 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.412 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.709 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.219 |
MOD_NEK2_1 | 718 | 723 | PF00069 | 0.392 |
MOD_NEK2_1 | 728 | 733 | PF00069 | 0.388 |
MOD_NEK2_1 | 755 | 760 | PF00069 | 0.416 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.470 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.342 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.258 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.258 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.657 |
MOD_PIKK_1 | 684 | 690 | PF00454 | 0.303 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.310 |
MOD_PK_1 | 214 | 220 | PF00069 | 0.187 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.187 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.514 |
MOD_PKA_2 | 723 | 729 | PF00069 | 0.348 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.319 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.268 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.394 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.469 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.258 |
MOD_Plk_1 | 718 | 724 | PF00069 | 0.138 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.358 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.421 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.306 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.319 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.461 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.580 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.278 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.324 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.598 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.524 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.274 |
MOD_Plk_4 | 736 | 742 | PF00069 | 0.239 |
MOD_Plk_4 | 751 | 757 | PF00069 | 0.319 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.520 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.401 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.390 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.507 |
MOD_SUMO_for_1 | 804 | 807 | PF00179 | 0.419 |
TRG_DiLeu_BaEn_1 | 106 | 111 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_1 | 763 | 768 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.299 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 155 | 157 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 545 | 547 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 650 | 652 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 789 | 791 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.485 |
TRG_NES_CRM1_1 | 539 | 553 | PF08389 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 108 | 112 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 651 | 656 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V0 | Leptomonas seymouri | 41% | 100% |
A0A0N0P8Y1 | Leptomonas seymouri | 75% | 100% |
A0A0N0P9D2 | Leptomonas seymouri | 38% | 100% |
A0A0N1I0Z0 | Leptomonas seymouri | 34% | 74% |
A0A0N1IKA7 | Leptomonas seymouri | 34% | 89% |
A0A0N1PEU4 | Leptomonas seymouri | 36% | 85% |
A0A0S4IQ76 | Bodo saltans | 48% | 100% |
A0A0S4IR78 | Bodo saltans | 37% | 92% |
A0A0S4IS51 | Bodo saltans | 36% | 100% |
A0A0S4ITR4 | Bodo saltans | 34% | 75% |
A0A0S4IWU8 | Bodo saltans | 37% | 95% |
A0A0S4J157 | Bodo saltans | 43% | 100% |
A0A0S4JCY8 | Bodo saltans | 37% | 79% |
A0A1X0NJ46 | Trypanosomatidae | 43% | 100% |
A0A1X0NKY7 | Trypanosomatidae | 34% | 76% |
A0A1X0NVG5 | Trypanosomatidae | 36% | 76% |
A0A1X0P0D7 | Trypanosomatidae | 38% | 100% |
A0A1X0P872 | Trypanosomatidae | 38% | 91% |
A0A1X0P9K6 | Trypanosomatidae | 57% | 100% |
A0A3Q8IEC9 | Leishmania donovani | 33% | 74% |
A0A3Q8II71 | Leishmania donovani | 94% | 100% |
A0A3Q8IJ24 | Leishmania donovani | 36% | 86% |
A0A3Q8IWG4 | Leishmania donovani | 32% | 100% |
A0A3R7MA90 | Trypanosoma rangeli | 44% | 100% |
A0A3R7MM88 | Trypanosoma rangeli | 33% | 100% |
A0A3R7NT42 | Trypanosoma rangeli | 57% | 100% |
A0A3S7WYA1 | Leishmania donovani | 36% | 74% |
A0A3S7X8Z5 | Leishmania donovani | 42% | 100% |
A0A3S7XB01 | Leishmania donovani | 34% | 74% |
A0A422MXB1 | Trypanosoma rangeli | 34% | 76% |
A0A422N8L3 | Trypanosoma rangeli | 35% | 79% |
A4HAT8 | Leishmania braziliensis | 88% | 100% |
A4HDG6 | Leishmania braziliensis | 35% | 74% |
A4HME2 | Leishmania braziliensis | 42% | 96% |
A4HNU7 | Leishmania braziliensis | 36% | 100% |
A4HPE9 | Leishmania braziliensis | 33% | 75% |
A4HQ83 | Leishmania braziliensis | 36% | 100% |
A4I009 | Leishmania infantum | 32% | 74% |
A4I0U7 | Leishmania infantum | 36% | 74% |
A4IA06 | Leishmania infantum | 95% | 100% |
A4IB14 | Leishmania infantum | 42% | 100% |
A4ICJ0 | Leishmania infantum | 34% | 74% |
A4ICP7 | Leishmania infantum | 36% | 86% |
A4IDY1 | Leishmania infantum | 32% | 100% |
C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 92% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 76% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 77% |
D4A2Z8 | Rattus norvegicus | 29% | 81% |
E9AEU3 | Leishmania major | 41% | 94% |
E9AIQ7 | Leishmania braziliensis | 32% | 75% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 74% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 94% |
E9AVY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 74% |
E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 99% |
F4HYJ7 | Arabidopsis thaliana | 31% | 68% |
F4IE66 | Arabidopsis thaliana | 33% | 100% |
F4IJV4 | Arabidopsis thaliana | 38% | 77% |
F4ILR7 | Arabidopsis thaliana | 35% | 81% |
F4IM84 | Arabidopsis thaliana | 33% | 73% |
F4JMJ3 | Arabidopsis thaliana | 38% | 92% |
F4JRJ6 | Arabidopsis thaliana | 38% | 100% |
O22899 | Arabidopsis thaliana | 43% | 100% |
O35286 | Mus musculus | 41% | 100% |
O42643 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 69% |
O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 43% | 100% |
O43143 | Homo sapiens | 41% | 100% |
O45244 | Caenorhabditis elegans | 39% | 80% |
O51767 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 30% | 98% |
O60231 | Homo sapiens | 39% | 78% |
P0C9A4 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 27% | 84% |
P15938 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 76% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 92% |
P24384 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 71% |
P34305 | Caenorhabditis elegans | 33% | 70% |
P34498 | Caenorhabditis elegans | 35% | 72% |
P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 42% | 100% |
Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
Q05B79 | Bos taurus | 30% | 80% |
Q09530 | Caenorhabditis elegans | 38% | 67% |
Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 77% |
Q14147 | Homo sapiens | 37% | 71% |
Q14562 | Homo sapiens | 38% | 66% |
Q20875 | Caenorhabditis elegans | 41% | 100% |
Q2NKY8 | Bos taurus | 29% | 66% |
Q38953 | Arabidopsis thaliana | 39% | 69% |
Q3ZBE0 | Bos taurus | 32% | 100% |
Q4Q0J4 | Leishmania major | 33% | 94% |
Q4Q1D7 | Leishmania major | 34% | 74% |
Q4Q1Y9 | Leishmania major | 37% | 100% |
Q4Q2X4 | Leishmania major | 93% | 100% |
Q4QAM3 | Leishmania major | 36% | 71% |
Q4QBJ7 | Leishmania major | 33% | 74% |
Q54F05 | Dictyostelium discoideum | 38% | 70% |
Q54MH3 | Dictyostelium discoideum | 39% | 73% |
Q54NJ4 | Dictyostelium discoideum | 41% | 100% |
Q5BJS0 | Rattus norvegicus | 29% | 68% |
Q5R607 | Pongo abelii | 28% | 68% |
Q5R864 | Pongo abelii | 35% | 100% |
Q5RAZ4 | Pongo abelii | 41% | 100% |
Q5RBD4 | Pongo abelii | 38% | 100% |
Q5UQ96 | Acanthamoeba polyphaga mimivirus | 27% | 100% |
Q5XH12 | Xenopus laevis | 28% | 100% |
Q5XI69 | Rattus norvegicus | 35% | 100% |
Q6PE54 | Mus musculus | 34% | 100% |
Q767K6 | Sus scrofa | 40% | 77% |
Q7K3M5 | Drosophila melanogaster | 41% | 100% |
Q7L2E3 | Homo sapiens | 29% | 68% |
Q7L7V1 | Homo sapiens | 28% | 100% |
Q7YR39 | Pan troglodytes | 39% | 77% |
Q80VY9 | Mus musculus | 36% | 100% |
Q8BZS9 | Mus musculus | 28% | 100% |
Q8IX18 | Homo sapiens | 35% | 100% |
Q8TE96 | Homo sapiens | 30% | 100% |
Q8VHK9 | Mus musculus | 29% | 81% |
Q8VY00 | Arabidopsis thaliana | 38% | 77% |
Q924H9 | Mus musculus | 31% | 100% |
Q93Y16 | Arabidopsis thaliana | 36% | 100% |
Q99PU8 | Mus musculus | 29% | 66% |
Q9BKQ8 | Caenorhabditis elegans | 36% | 100% |
Q9DBV3 | Mus musculus | 35% | 71% |
Q9H2U1 | Homo sapiens | 29% | 80% |
Q9H5Z1 | Homo sapiens | 38% | 100% |
Q9H6R0 | Homo sapiens | 36% | 100% |
Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 68% |
Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q9LZQ9 | Arabidopsis thaliana | 42% | 100% |
Q9P774 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 69% |
V5B3L7 | Trypanosoma cruzi | 36% | 100% |
V5B7H6 | Trypanosoma cruzi | 31% | 74% |
V5BKH2 | Trypanosoma cruzi | 57% | 100% |
V5BPV3 | Trypanosoma cruzi | 34% | 77% |
V5BV22 | Trypanosoma cruzi | 39% | 91% |
V5C0I9 | Trypanosoma cruzi | 35% | 100% |
V5D886 | Trypanosoma cruzi | 43% | 100% |