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:0005635 | nuclear envelope | 4 | 5 |
GO:0005783 | endoplasmic reticulum | 5 | 5 |
GO:0016020 | membrane | 2 | 27 |
GO:0031967 | organelle envelope | 3 | 5 |
GO:0031975 | envelope | 2 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
Related structures:
AlphaFold database: E9AET7
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 | 582 | 586 | PF00656 | 0.312 |
CLV_MEL_PAP_1 | 491 | 497 | PF00089 | 0.250 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.296 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.602 |
CLV_Separin_Metazoa | 275 | 279 | PF03568 | 0.284 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.279 |
DEG_ODPH_VHL_1 | 312 | 325 | PF01847 | 0.367 |
DEG_SCF_FBW7_1 | 506 | 512 | PF00400 | 0.213 |
DEG_SPOP_SBC_1 | 69 | 73 | PF00917 | 0.474 |
DOC_AGCK_PIF_1 | 357 | 362 | PF00069 | 0.224 |
DOC_AGCK_PIF_2 | 54 | 59 | PF00069 | 0.293 |
DOC_CKS1_1 | 506 | 511 | PF01111 | 0.224 |
DOC_CYCLIN_RxL_1 | 323 | 333 | PF00134 | 0.254 |
DOC_CYCLIN_yCln2_LP_2 | 408 | 414 | PF00134 | 0.254 |
DOC_MAPK_DCC_7 | 483 | 493 | PF00069 | 0.530 |
DOC_MAPK_FxFP_2 | 360 | 363 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 278 | 285 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 286 | 295 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 381 | 390 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 480 | 488 | PF00069 | 0.639 |
DOC_MAPK_HePTP_8 | 285 | 297 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 288 | 297 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 494 | 501 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 527 | 533 | PF00149 | 0.385 |
DOC_PP1_RVXF_1 | 561 | 568 | PF00149 | 0.303 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.440 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.375 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.279 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.338 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 174 | 180 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.279 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 229 | 234 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 347 | 351 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 517 | 525 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 580 | 584 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 637 | 643 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 671 | 675 | PF00244 | 0.372 |
LIG_Actin_WH2_2 | 479 | 496 | PF00022 | 0.493 |
LIG_Actin_WH2_2 | 5 | 21 | PF00022 | 0.212 |
LIG_Actin_WH2_2 | 541 | 557 | PF00022 | 0.265 |
LIG_AP2alpha_2 | 34 | 36 | PF02296 | 0.279 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.380 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.264 |
LIG_deltaCOP1_diTrp_1 | 426 | 435 | PF00928 | 0.584 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.366 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.435 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.307 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.491 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.311 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.397 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.311 |
LIG_IRF3_LxIS_1 | 304 | 310 | PF10401 | 0.224 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 359 | 363 | PF02991 | 0.201 |
LIG_LIR_Apic_2 | 433 | 438 | PF02991 | 0.544 |
LIG_LIR_Apic_2 | 524 | 528 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 662 | 666 | PF02991 | 0.381 |
LIG_LIR_Apic_2 | 734 | 738 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 549 | 559 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 617 | 623 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 641 | 651 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 692 | 702 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 617 | 621 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 641 | 646 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 692 | 697 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 699 | 705 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.250 |
LIG_LYPXL_yS_3 | 74 | 77 | PF13949 | 0.375 |
LIG_MLH1_MIPbox_1 | 50 | 54 | PF16413 | 0.380 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.377 |
LIG_PCNA_PIPBox_1 | 541 | 550 | PF02747 | 0.288 |
LIG_PCNA_yPIPBox_3 | 541 | 555 | PF02747 | 0.276 |
LIG_Pex14_1 | 50 | 54 | PF04695 | 0.279 |
LIG_Pex14_1 | 568 | 572 | PF04695 | 0.293 |
LIG_Pex14_2 | 33 | 37 | PF04695 | 0.258 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.385 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.215 |
LIG_PTB_Apo_2 | 637 | 644 | PF02174 | 0.320 |
LIG_PTB_Phospho_1 | 637 | 643 | PF10480 | 0.315 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.293 |
LIG_SH2_CRK | 663 | 667 | PF00017 | 0.382 |
LIG_SH2_CRK | 702 | 706 | PF00017 | 0.293 |
LIG_SH2_NCK_1 | 663 | 667 | PF00017 | 0.339 |
LIG_SH2_PTP2 | 199 | 202 | PF00017 | 0.351 |
LIG_SH2_PTP2 | 618 | 621 | PF00017 | 0.282 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.313 |
LIG_SH2_SRC | 547 | 550 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.202 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 698 | 702 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 510 | 513 | PF00017 | 0.468 |
LIG_SH2_STAT3 | 570 | 573 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.282 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.414 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.343 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.477 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.411 |
LIG_SH3_3 | 718 | 724 | PF00018 | 0.361 |
LIG_SH3_3 | 725 | 731 | PF00018 | 0.364 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.375 |
LIG_SUMO_SIM_anti_2 | 115 | 120 | PF11976 | 0.409 |
LIG_SUMO_SIM_anti_2 | 403 | 409 | PF11976 | 0.209 |
LIG_SUMO_SIM_par_1 | 113 | 120 | PF11976 | 0.259 |
LIG_SUMO_SIM_par_1 | 500 | 505 | PF11976 | 0.389 |
LIG_SxIP_EBH_1 | 133 | 146 | PF03271 | 0.349 |
LIG_TYR_ITSM | 163 | 170 | PF00017 | 0.316 |
LIG_UBA3_1 | 674 | 683 | PF00899 | 0.398 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.449 |
MOD_CDC14_SPxK_1 | 251 | 254 | PF00782 | 0.380 |
MOD_CDK_SPK_2 | 347 | 352 | PF00069 | 0.177 |
MOD_CDK_SPxK_1 | 248 | 254 | PF00069 | 0.279 |
MOD_CDK_SPxxK_3 | 664 | 671 | PF00069 | 0.376 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.351 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.224 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.338 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.333 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.334 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.247 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.402 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.278 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.497 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.370 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.420 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.570 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.565 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.582 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.569 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.342 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.521 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.297 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.621 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.634 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.343 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.738 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.282 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.505 |
MOD_N-GLC_1 | 711 | 716 | PF02516 | 0.531 |
MOD_N-GLC_2 | 154 | 156 | PF02516 | 0.279 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.435 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.295 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.362 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.355 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.214 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.290 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.249 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.309 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.299 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.456 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.346 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.329 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.290 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.321 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.332 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.316 |
MOD_NEK2_2 | 478 | 483 | PF00069 | 0.522 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.773 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.308 |
MOD_PK_1 | 19 | 25 | PF00069 | 0.314 |
MOD_PK_1 | 296 | 302 | PF00069 | 0.417 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.315 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.531 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.247 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.477 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.295 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.310 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.367 |
MOD_PKB_1 | 294 | 302 | PF00069 | 0.513 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.231 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.317 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.316 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.423 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.423 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.342 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.320 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.279 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.362 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.305 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.360 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.274 |
MOD_Plk_4 | 731 | 737 | PF00069 | 0.366 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.279 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.232 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.495 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.473 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.329 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.311 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.338 |
MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.323 |
TRG_DiLeu_BaEn_1 | 607 | 612 | PF01217 | 0.320 |
TRG_DiLeu_BaEn_2 | 382 | 388 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.283 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.257 |
TRG_NES_CRM1_1 | 257 | 272 | PF08389 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 326 | 331 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 52% | 94% |
A0A1X0NFU7 | Trypanosomatidae | 59% | 91% |
A0A3Q8IHT0 | Leishmania donovani | 77% | 90% |
A0A3Q8II34 | Leishmania donovani | 58% | 97% |
A0A3Q8ILY7 | Leishmania donovani | 92% | 99% |
A0A3Q8IV37 | Leishmania donovani | 75% | 92% |
A0A422MX14 | Trypanosoma rangeli | 58% | 93% |
A4HFF9 | Leishmania braziliensis | 69% | 90% |
A4HMD5 | Leishmania braziliensis | 82% | 100% |
A4HMD6 | Leishmania braziliensis | 57% | 94% |
A4HMD7 | Leishmania braziliensis | 71% | 91% |
A4IB08 | Leishmania infantum | 77% | 90% |
A4IB09 | Leishmania infantum | 93% | 99% |
A4IB10 | Leishmania infantum | 58% | 97% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 94% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E2RG47 | Canis lupus familiaris | 30% | 94% |
E9AET6 | Leishmania major | 79% | 100% |
E9AET8 | Leishmania major | 59% | 98% |
E9AET9 | Leishmania major | 76% | 90% |
E9AHU4 | Leishmania infantum | 75% | 92% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 90% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 92% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 97% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 91% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P46975 | Caenorhabditis elegans | 31% | 100% |
P46977 | Homo sapiens | 29% | 100% |
P46978 | Mus musculus | 29% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 31% | 94% |
Q54NM9 | Dictyostelium discoideum | 31% | 100% |
Q5RCE2 | Pongo abelii | 29% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 31% | 94% |
Q93ZY3 | Arabidopsis thaliana | 32% | 99% |
Q9FX21 | Arabidopsis thaliana | 30% | 100% |
V5BDM6 | Trypanosoma cruzi | 57% | 93% |