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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H6Z1
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0035966 | response to topologically incorrect protein | 3 | 1 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0051788 | response to misfolded protein | 4 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071218 | cellular response to misfolded protein | 5 | 1 |
GO:0071310 | cellular response to organic substance | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0030544 | Hsp70 protein binding | 4 | 1 |
GO:0031072 | heat shock protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.430 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 727 | 729 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 261 | 265 | PF00082 | 0.522 |
CLV_PCSK_FUR_1 | 553 | 557 | PF00082 | 0.526 |
CLV_PCSK_FUR_1 | 630 | 634 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 555 | 557 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.220 |
CLV_PCSK_PC1ET2_1 | 555 | 557 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 487 | 491 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.444 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.465 |
DEG_SPOP_SBC_1 | 163 | 167 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 313 | 317 | PF00917 | 0.502 |
DEG_SPOP_SBC_1 | 488 | 492 | PF00917 | 0.558 |
DEG_SPOP_SBC_1 | 684 | 688 | PF00917 | 0.546 |
DOC_CKS1_1 | 716 | 721 | PF01111 | 0.467 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.420 |
DOC_CYCLIN_RxL_1 | 115 | 128 | PF00134 | 0.400 |
DOC_CYCLIN_RxL_1 | 200 | 209 | PF00134 | 0.465 |
DOC_CYCLIN_RxL_1 | 630 | 640 | PF00134 | 0.335 |
DOC_CYCLIN_yClb1_LxF_4 | 68 | 73 | PF00134 | 0.515 |
DOC_MAPK_gen_1 | 115 | 125 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 382 | 390 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 630 | 637 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 631 | 638 | PF00149 | 0.341 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.438 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.371 |
DOC_USP7_MATH_2 | 335 | 341 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 461 | 465 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 540 | 545 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 665 | 670 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 305 | 313 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 634 | 644 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 697 | 707 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 98 | 104 | PF00244 | 0.359 |
LIG_APCC_ABBA_1 | 123 | 128 | PF00400 | 0.309 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.664 |
LIG_BRCT_BRCA1_1 | 415 | 419 | PF00533 | 0.490 |
LIG_eIF4E_1 | 118 | 124 | PF01652 | 0.308 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.423 |
LIG_EVH1_1 | 32 | 36 | PF00568 | 0.435 |
LIG_EVH1_1 | 71 | 75 | PF00568 | 0.497 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.379 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.450 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.539 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.674 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.678 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.514 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.594 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.618 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.588 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.511 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.427 |
LIG_Integrin_RGD_1 | 234 | 236 | PF01839 | 0.553 |
LIG_LIR_Gen_1 | 25 | 35 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 603 | 614 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 676 | 684 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 574 | 578 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 676 | 681 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.308 |
LIG_NRBOX | 721 | 727 | PF00104 | 0.460 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.308 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.427 |
LIG_SH2_SRC | 144 | 147 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.347 |
LIG_SH3_1 | 666 | 672 | PF00018 | 0.541 |
LIG_SH3_1 | 713 | 719 | PF00018 | 0.478 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.650 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.521 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.610 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.567 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.567 |
LIG_SH3_3 | 713 | 719 | PF00018 | 0.504 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.427 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.489 |
LIG_TYR_ITSM | 23 | 30 | PF00017 | 0.416 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.412 |
LIG_WRC_WIRS_1 | 49 | 54 | PF05994 | 0.438 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.619 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.646 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.572 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.690 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.655 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.607 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.613 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.627 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.759 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.464 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.650 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.496 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.527 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.577 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.512 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.534 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.566 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.633 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.600 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.771 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.544 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.591 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.456 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.434 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.387 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.773 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.442 |
MOD_DYRK1A_RPxSP_1 | 62 | 66 | PF00069 | 0.522 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.548 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.555 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.782 |
MOD_GlcNHglycan | 276 | 280 | PF01048 | 0.648 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.572 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.572 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.573 |
MOD_GlcNHglycan | 396 | 400 | PF01048 | 0.626 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.683 |
MOD_GlcNHglycan | 497 | 502 | PF01048 | 0.691 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.621 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.507 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.577 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.492 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.518 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.428 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.608 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.493 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.656 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.452 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.528 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.646 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.573 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.577 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.684 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.559 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.537 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.564 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.628 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.578 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.562 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.544 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.521 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.675 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.564 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.522 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.495 |
MOD_LATS_1 | 303 | 309 | PF00433 | 0.531 |
MOD_LATS_1 | 408 | 414 | PF00433 | 0.473 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.500 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.397 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.560 |
MOD_N-GLC_2 | 245 | 247 | PF02516 | 0.657 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.435 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.683 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.612 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.702 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.430 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.502 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.461 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.660 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.616 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.545 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.543 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.378 |
MOD_PKA_1 | 464 | 470 | PF00069 | 0.625 |
MOD_PKA_1 | 55 | 61 | PF00069 | 0.506 |
MOD_PKA_1 | 555 | 561 | PF00069 | 0.411 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.611 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.710 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.541 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.519 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.426 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.522 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.691 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.443 |
MOD_Plk_2-3 | 238 | 244 | PF00069 | 0.594 |
MOD_Plk_2-3 | 337 | 343 | PF00069 | 0.705 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.491 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.462 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.507 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.671 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.607 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.698 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.541 |
MOD_ProDKin_1 | 540 | 546 | PF00069 | 0.517 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.575 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.615 |
MOD_ProDKin_1 | 665 | 671 | PF00069 | 0.598 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.527 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 453 | 456 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 455 | 463 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 77 | 86 | PF00179 | 0.482 |
TRG_DiLeu_BaEn_1 | 135 | 140 | PF01217 | 0.225 |
TRG_DiLeu_BaLyEn_6 | 566 | 571 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.381 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 629 | 632 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 633 | 635 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 726 | 728 | PF00400 | 0.451 |
TRG_NLS_MonoExtN_4 | 116 | 123 | PF00514 | 0.225 |
TRG_Pf-PMV_PEXEL_1 | 568 | 572 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC79 | Leptomonas seymouri | 38% | 100% |
A0A3S7WS81 | Leishmania donovani | 61% | 100% |
E9AGH2 | Leishmania infantum | 61% | 100% |
E9AP11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
Q4QGH8 | Leishmania major | 60% | 100% |