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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0034045 | phagophore assembly site membrane | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000407 | phagophore assembly site | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005776 | autophagosome | 6 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0000502 | proteasome complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
GO:1905369 | endopeptidase complex | 4 | 2 |
Related structures:
AlphaFold database: E9AIS5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006869 | lipid transport | 5 | 12 |
GO:0006914 | autophagy | 3 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0000422 | autophagy of mitochondrion | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007005 | mitochondrion organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0034497 | protein localization to phagophore assembly site | 5 | 1 |
GO:0044804 | autophagy of nucleus | 4 | 1 |
GO:0044805 | late nucleophagy | 5 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0061726 | mitochondrion disassembly | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1903008 | organelle disassembly | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 529 | 533 | PF00656 | 0.673 |
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.639 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.194 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.194 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 567 | 569 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.473 |
CLV_Separin_Metazoa | 124 | 128 | PF03568 | 0.459 |
DEG_APCC_DBOX_1 | 639 | 647 | PF00400 | 0.564 |
DOC_CDC14_PxL_1 | 413 | 421 | PF14671 | 0.403 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 477 | 483 | PF00134 | 0.277 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.276 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 463 | 470 | PF00069 | 0.251 |
DOC_MAPK_gen_1 | 567 | 576 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 613 | 619 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 463 | 470 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 488 | 496 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 567 | 576 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.258 |
DOC_PP2B_LxvP_1 | 94 | 97 | PF13499 | 0.313 |
DOC_PP4_FxxP_1 | 151 | 154 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.707 |
DOC_USP7_MATH_2 | 528 | 534 | PF00917 | 0.619 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.275 |
DOC_USP7_UBL2_3 | 567 | 571 | PF12436 | 0.535 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.579 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 157 | 161 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 322 | 332 | PF00244 | 0.242 |
LIG_14-3-3_CanoR_1 | 361 | 370 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 372 | 380 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.665 |
LIG_Actin_WH2_2 | 2 | 20 | PF00022 | 0.623 |
LIG_Actin_WH2_2 | 575 | 591 | PF00022 | 0.588 |
LIG_Actin_WH2_2 | 690 | 707 | PF00022 | 0.454 |
LIG_APCC_ABBA_1 | 332 | 337 | PF00400 | 0.210 |
LIG_APCC_ABBAyCdc20_2 | 331 | 337 | PF00400 | 0.313 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.669 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.516 |
LIG_CaM_NSCaTE_8 | 45 | 52 | PF13499 | 0.357 |
LIG_Clathr_ClatBox_1 | 225 | 229 | PF01394 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 327 | 332 | PF00928 | 0.265 |
LIG_eIF4E_1 | 289 | 295 | PF01652 | 0.363 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.396 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.367 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.447 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.434 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.494 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.497 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.272 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.313 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.363 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.700 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.701 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.254 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.513 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.718 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.679 |
LIG_FHA_2 | 655 | 661 | PF00498 | 0.761 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.603 |
LIG_HP1_1 | 480 | 484 | PF01393 | 0.170 |
LIG_IRF3_LxIS_1 | 387 | 394 | PF10401 | 0.241 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 206 | 212 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 385 | 389 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 120 | 129 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 259 | 268 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.212 |
LIG_LIR_Gen_1 | 578 | 583 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.424 |
LIG_MYND_1 | 417 | 421 | PF01753 | 0.157 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.254 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.606 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.282 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.357 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.213 |
LIG_Rb_pABgroove_1 | 256 | 264 | PF01858 | 0.410 |
LIG_REV1ctd_RIR_1 | 459 | 469 | PF16727 | 0.313 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.306 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.275 |
LIG_SH2_NCK_1 | 335 | 339 | PF00017 | 0.220 |
LIG_SH2_NCK_1 | 413 | 417 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.360 |
LIG_SH2_NCK_1 | 454 | 458 | PF00017 | 0.267 |
LIG_SH2_PTP2 | 248 | 251 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 299 | 302 | PF00017 | 0.389 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.484 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 132 | 135 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.313 |
LIG_SH3_2 | 215 | 220 | PF14604 | 0.513 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.513 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.592 |
LIG_SUMO_SIM_anti_2 | 407 | 412 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 491 | 497 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 695 | 701 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 181 | 187 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.513 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.614 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.389 |
LIG_UBA3_1 | 301 | 307 | PF00899 | 0.189 |
LIG_Vh1_VBS_1 | 111 | 129 | PF01044 | 0.170 |
LIG_WRC_WIRS_1 | 383 | 388 | PF05994 | 0.277 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.305 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.291 |
MOD_CDK_SPxxK_3 | 150 | 157 | PF00069 | 0.258 |
MOD_CDK_SPxxK_3 | 596 | 603 | PF00069 | 0.461 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.277 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.421 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.718 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.293 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.414 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.664 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.677 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.653 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.674 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.484 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.277 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.434 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.571 |
MOD_CK2_1 | 654 | 660 | PF00069 | 0.614 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.534 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.386 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.286 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.389 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.451 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.365 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.181 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.244 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.389 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.707 |
MOD_GlcNHglycan | 549 | 553 | PF01048 | 0.447 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.636 |
MOD_GlcNHglycan | 672 | 676 | PF01048 | 0.629 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.344 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.318 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.234 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.389 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.262 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.633 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.611 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.603 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.651 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.664 |
MOD_N-GLC_1 | 536 | 541 | PF02516 | 0.693 |
MOD_N-GLC_2 | 375 | 377 | PF02516 | 0.170 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.302 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.186 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.255 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.526 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.356 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.365 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.201 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.312 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.327 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.451 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.273 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.217 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.340 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.534 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.357 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.272 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.354 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.412 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.416 |
MOD_NEK2_2 | 398 | 403 | PF00069 | 0.170 |
MOD_NEK2_2 | 645 | 650 | PF00069 | 0.743 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.305 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.412 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.322 |
MOD_PIKK_1 | 622 | 628 | PF00454 | 0.456 |
MOD_PIKK_1 | 692 | 698 | PF00454 | 0.443 |
MOD_PK_1 | 203 | 209 | PF00069 | 0.389 |
MOD_PK_1 | 488 | 494 | PF00069 | 0.254 |
MOD_PK_1 | 613 | 619 | PF00069 | 0.284 |
MOD_PKA_1 | 613 | 619 | PF00069 | 0.284 |
MOD_PKA_1 | 653 | 659 | PF00069 | 0.488 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.383 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.554 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.329 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.389 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.397 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.599 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.548 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.683 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.648 |
MOD_PKA_2 | 704 | 710 | PF00069 | 0.601 |
MOD_PKA_2 | 716 | 722 | PF00069 | 0.672 |
MOD_Plk_1 | 516 | 522 | PF00069 | 0.533 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.464 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.576 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.307 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.371 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.327 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.283 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.293 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.376 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.310 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.277 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.313 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.329 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.614 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.334 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.265 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.697 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.393 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.244 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.305 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.629 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.481 |
TRG_DiLeu_BaEn_2 | 123 | 129 | PF01217 | 0.258 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.203 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.225 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.140 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.290 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.185 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.217 |
TRG_ER_diArg_1 | 465 | 468 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.625 |
TRG_NES_CRM1_1 | 217 | 229 | PF08389 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 467 | 472 | PF00026 | 0.170 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5S4 | Leptomonas seymouri | 65% | 100% |
A0A0S4JRE4 | Bodo saltans | 28% | 92% |
A0A1X0P5B9 | Trypanosomatidae | 35% | 100% |
A0A3S5H7H3 | Leishmania donovani | 83% | 99% |
A0A422NTE4 | Trypanosoma rangeli | 35% | 100% |
D0A5N9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AD16 | Leishmania major | 81% | 100% |
E9AHC0 | Leishmania infantum | 83% | 99% |
E9AYU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
P0CM40 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 20% | 83% |
P0CM41 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 20% | 83% |
Q8RUS5 | Arabidopsis thaliana | 21% | 84% |
V5B7I2 | Trypanosoma cruzi | 34% | 100% |