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: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: E9B5Z3
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 500 | 504 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 636 | 640 | PF00656 | 0.314 |
CLV_MEL_PAP_1 | 545 | 551 | PF00089 | 0.254 |
CLV_MEL_PAP_1 | 805 | 811 | PF00089 | 0.474 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 819 | 821 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 522 | 524 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 819 | 821 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 820 | 824 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 830 | 834 | PF00082 | 0.500 |
CLV_Separin_Metazoa | 329 | 333 | PF03568 | 0.285 |
DEG_SCF_FBW7_1 | 560 | 566 | PF00400 | 0.213 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.474 |
DOC_AGCK_PIF_1 | 411 | 416 | PF00069 | 0.225 |
DOC_AGCK_PIF_2 | 108 | 113 | PF00069 | 0.294 |
DOC_CKS1_1 | 560 | 565 | PF01111 | 0.225 |
DOC_CYCLIN_RxL_1 | 377 | 387 | PF00134 | 0.255 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.255 |
DOC_MAPK_gen_1 | 228 | 237 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 332 | 339 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 435 | 444 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 542 | 551 | PF00069 | 0.611 |
DOC_PP1_RVXF_1 | 581 | 587 | PF00149 | 0.395 |
DOC_PP1_RVXF_1 | 615 | 622 | PF00149 | 0.303 |
DOC_PP1_RVXF_1 | 806 | 812 | PF00149 | 0.288 |
DOC_PP2B_LxvP_1 | 365 | 368 | PF13499 | 0.207 |
DOC_PP4_FxxP_1 | 579 | 582 | PF00568 | 0.385 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.280 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.364 |
DOC_USP7_UBL2_3 | 402 | 406 | PF12436 | 0.156 |
DOC_USP7_UBL2_3 | 830 | 834 | PF12436 | 0.299 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 683 | 688 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.325 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 23 | 28 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 274 | 278 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 283 | 288 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 401 | 405 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 523 | 533 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 571 | 579 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 634 | 638 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 691 | 697 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 725 | 729 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 808 | 812 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 820 | 825 | PF00244 | 0.387 |
LIG_Actin_WH2_2 | 51 | 69 | PF00022 | 0.202 |
LIG_Actin_WH2_2 | 533 | 550 | PF00022 | 0.494 |
LIG_Actin_WH2_2 | 595 | 611 | PF00022 | 0.268 |
LIG_AP2alpha_2 | 88 | 90 | PF02296 | 0.280 |
LIG_BRCT_BRCA1_1 | 104 | 108 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.565 |
LIG_CSL_BTD_1 | 418 | 421 | PF09270 | 0.160 |
LIG_deltaCOP1_diTrp_1 | 480 | 489 | PF00928 | 0.584 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.367 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.307 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.492 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.313 |
LIG_FHA_1 | 736 | 742 | PF00498 | 0.392 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.248 |
LIG_FHA_2 | 821 | 827 | PF00498 | 0.345 |
LIG_LIR_Apic_2 | 487 | 492 | PF02991 | 0.553 |
LIG_LIR_Apic_2 | 578 | 582 | PF02991 | 0.390 |
LIG_LIR_Apic_2 | 716 | 720 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 788 | 792 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 101 | 111 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 190 | 199 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 219 | 227 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 480 | 490 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 603 | 613 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 671 | 677 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 695 | 705 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 746 | 756 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 810 | 817 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 480 | 486 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 671 | 675 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 695 | 700 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 746 | 751 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 753 | 759 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 810 | 814 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.280 |
LIG_LYPXL_yS_3 | 128 | 131 | PF13949 | 0.376 |
LIG_MLH1_MIPbox_1 | 104 | 108 | PF16413 | 0.381 |
LIG_NRBOX | 312 | 318 | PF00104 | 0.378 |
LIG_PDZ_Class_1 | 833 | 838 | PF00595 | 0.320 |
LIG_Pex14_1 | 104 | 108 | PF04695 | 0.280 |
LIG_Pex14_1 | 564 | 568 | PF04695 | 0.276 |
LIG_Pex14_1 | 622 | 626 | PF04695 | 0.292 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.216 |
LIG_Pex14_2 | 410 | 414 | PF04695 | 0.386 |
LIG_Pex14_2 | 87 | 91 | PF04695 | 0.259 |
LIG_PTB_Apo_2 | 691 | 698 | PF02174 | 0.324 |
LIG_PTB_Phospho_1 | 691 | 697 | PF10480 | 0.320 |
LIG_SH2_CRK | 717 | 721 | PF00017 | 0.379 |
LIG_SH2_CRK | 756 | 760 | PF00017 | 0.293 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.294 |
LIG_SH2_NCK_1 | 445 | 449 | PF00017 | 0.195 |
LIG_SH2_PTP2 | 253 | 256 | PF00017 | 0.352 |
LIG_SH2_PTP2 | 672 | 675 | PF00017 | 0.284 |
LIG_SH2_SRC | 601 | 604 | PF00017 | 0.300 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.203 |
LIG_SH2_STAP1 | 416 | 420 | PF00017 | 0.194 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.237 |
LIG_SH2_STAP1 | 752 | 756 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 624 | 627 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 828 | 831 | PF00017 | 0.284 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.376 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.415 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.478 |
LIG_SH3_3 | 699 | 705 | PF00018 | 0.412 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.359 |
LIG_SH3_3 | 779 | 785 | PF00018 | 0.363 |
LIG_SUMO_SIM_anti_2 | 457 | 463 | PF11976 | 0.209 |
LIG_SUMO_SIM_par_1 | 167 | 174 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.218 |
LIG_SUMO_SIM_par_1 | 554 | 559 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 73 | 79 | PF11976 | 0.314 |
LIG_SxIP_EBH_1 | 187 | 200 | PF03271 | 0.350 |
LIG_TRAF2_1 | 592 | 595 | PF00917 | 0.250 |
LIG_TYR_ITSM | 217 | 224 | PF00017 | 0.317 |
LIG_UBA3_1 | 59 | 67 | PF00899 | 0.299 |
LIG_UBA3_1 | 728 | 737 | PF00899 | 0.394 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.317 |
LIG_WRC_WIRS_1 | 59 | 64 | PF05994 | 0.483 |
MOD_CDC14_SPxK_1 | 305 | 308 | PF00782 | 0.381 |
MOD_CDK_SPK_2 | 401 | 406 | PF00069 | 0.178 |
MOD_CDK_SPK_2 | 609 | 614 | PF00069 | 0.245 |
MOD_CDK_SPxK_1 | 302 | 308 | PF00069 | 0.280 |
MOD_CDK_SPxxK_3 | 718 | 725 | PF00069 | 0.373 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.298 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.352 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.720 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.662 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.225 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.709 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.668 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.348 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.284 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.332 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.541 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.247 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.403 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.699 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.318 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.391 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.570 |
MOD_GlcNHglycan | 176 | 180 | PF01048 | 0.498 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.349 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.505 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.379 |
MOD_GlcNHglycan | 506 | 510 | PF01048 | 0.568 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.575 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.421 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.585 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.566 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.528 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.343 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.699 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.522 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.298 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.643 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.590 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.274 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.628 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.640 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.747 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.283 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.331 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.277 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.344 |
MOD_N-GLC_1 | 632 | 637 | PF02516 | 0.508 |
MOD_N-GLC_1 | 765 | 770 | PF02516 | 0.527 |
MOD_N-GLC_2 | 208 | 210 | PF02516 | 0.280 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.333 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.363 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.356 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.214 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.250 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.310 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.661 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.330 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.341 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.289 |
MOD_NEK2_1 | 724 | 729 | PF00069 | 0.319 |
MOD_NEK2_2 | 223 | 228 | PF00069 | 0.317 |
MOD_NEK2_2 | 38 | 43 | PF00069 | 0.531 |
MOD_NEK2_2 | 532 | 537 | PF00069 | 0.522 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.569 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.799 |
MOD_PIKK_1 | 563 | 569 | PF00454 | 0.333 |
MOD_PK_1 | 73 | 79 | PF00069 | 0.315 |
MOD_PKA_1 | 820 | 826 | PF00069 | 0.323 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.579 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.316 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.532 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.247 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.478 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.294 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.313 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.365 |
MOD_PKA_2 | 807 | 813 | PF00069 | 0.318 |
MOD_PKB_1 | 348 | 356 | PF00069 | 0.513 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.232 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.319 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.280 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.317 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.424 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.424 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.317 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.321 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.364 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.310 |
MOD_Plk_4 | 724 | 730 | PF00069 | 0.358 |
MOD_Plk_4 | 743 | 749 | PF00069 | 0.269 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.365 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.280 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.233 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.511 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.474 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.328 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.313 |
MOD_ProDKin_1 | 683 | 689 | PF00069 | 0.341 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.320 |
MOD_SUMO_rev_2 | 826 | 835 | PF00179 | 0.297 |
TRG_DiLeu_BaEn_1 | 661 | 666 | PF01217 | 0.322 |
TRG_DiLeu_BaEn_2 | 436 | 442 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 70 | 75 | PF01217 | 0.267 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 756 | 759 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.294 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.412 |
TRG_NES_CRM1_1 | 311 | 326 | PF08389 | 0.381 |
TRG_NLS_MonoExtN_4 | 816 | 823 | PF00514 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 380 | 385 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 52% | 100% |
A0A1X0NFU7 | Trypanosomatidae | 55% | 99% |
A0A3Q8IHT0 | Leishmania donovani | 70% | 97% |
A0A3Q8II34 | Leishmania donovani | 57% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 88% | 100% |
A0A3Q8IV37 | Leishmania donovani | 74% | 100% |
A0A422MX14 | Trypanosoma rangeli | 57% | 100% |
A4HFF9 | Leishmania braziliensis | 69% | 100% |
A4HMD5 | Leishmania braziliensis | 80% | 100% |
A4HMD6 | Leishmania braziliensis | 55% | 100% |
A4HMD7 | Leishmania braziliensis | 71% | 100% |
A4IB08 | Leishmania infantum | 71% | 97% |
A4IB09 | Leishmania infantum | 88% | 100% |
A4IB10 | Leishmania infantum | 57% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E2RG47 | Canis lupus familiaris | 30% | 100% |
E9AET6 | Leishmania major | 75% | 100% |
E9AET7 | Leishmania major | 89% | 100% |
E9AET8 | Leishmania major | 57% | 100% |
E9AET9 | Leishmania major | 74% | 100% |
E9AHU4 | Leishmania infantum | 74% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 98% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P46975 | Caenorhabditis elegans | 30% | 100% |
P46977 | Homo sapiens | 30% | 100% |
P46978 | Mus musculus | 30% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 30% | 100% |
Q54NM9 | Dictyostelium discoideum | 30% | 100% |
Q5RCE2 | Pongo abelii | 30% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 30% | 100% |
Q93ZY3 | Arabidopsis thaliana | 32% | 100% |
Q9FX21 | Arabidopsis thaliana | 32% | 100% |
V5BDM6 | Trypanosoma cruzi | 57% | 100% |