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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HZ39
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 14 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 14 |
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0009056 | catabolic process | 2 | 14 |
GO:0009057 | macromolecule catabolic process | 4 | 14 |
GO:0009987 | cellular process | 1 | 14 |
GO:0016579 | protein deubiquitination | 6 | 14 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 14 |
GO:0036211 | protein modification process | 4 | 14 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0043412 | macromolecule modification | 4 | 14 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 14 |
GO:0044237 | cellular metabolic process | 2 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0044248 | cellular catabolic process | 3 | 14 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 14 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 14 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 14 |
GO:0070646 | protein modification by small protein removal | 5 | 14 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 14 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
GO:1901575 | organic substance catabolic process | 3 | 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 14 |
GO:0008233 | peptidase activity | 3 | 14 |
GO:0008234 | cysteine-type peptidase activity | 4 | 14 |
GO:0016787 | hydrolase activity | 2 | 14 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 14 |
GO:0101005 | deubiquitinase activity | 5 | 14 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 14 |
GO:0004175 | endopeptidase activity | 4 | 2 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.414 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.463 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 636 | 638 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 636 | 638 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.298 |
DEG_APCC_DBOX_1 | 635 | 643 | PF00400 | 0.391 |
DEG_APCC_KENBOX_2 | 418 | 422 | PF00400 | 0.264 |
DEG_SCF_FBW7_1 | 94 | 101 | PF00400 | 0.547 |
DEG_SPOP_SBC_1 | 601 | 605 | PF00917 | 0.384 |
DEG_SPOP_SBC_1 | 621 | 625 | PF00917 | 0.223 |
DEG_SPOP_SBC_1 | 707 | 711 | PF00917 | 0.309 |
DOC_MAPK_gen_1 | 396 | 403 | PF00069 | 0.264 |
DOC_MAPK_gen_1 | 559 | 566 | PF00069 | 0.267 |
DOC_MAPK_HePTP_8 | 477 | 489 | PF00069 | 0.391 |
DOC_MAPK_HePTP_8 | 556 | 568 | PF00069 | 0.280 |
DOC_MAPK_MEF2A_6 | 113 | 121 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 480 | 489 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 559 | 568 | PF00069 | 0.344 |
DOC_MAPK_RevD_3 | 531 | 547 | PF00069 | 0.306 |
DOC_PP4_FxxP_1 | 504 | 507 | PF00568 | 0.298 |
DOC_PP4_FxxP_1 | 698 | 701 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 100 | 105 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 188 | 193 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.527 |
LIG_APCC_ABBAyCdc20_2 | 480 | 486 | PF00400 | 0.391 |
LIG_BIR_III_4 | 703 | 707 | PF00653 | 0.391 |
LIG_BRCT_BRCA1_1 | 399 | 403 | PF00533 | 0.374 |
LIG_CaM_IQ_9 | 545 | 561 | PF13499 | 0.363 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.713 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.509 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.333 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.331 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.383 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.383 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.814 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.391 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.282 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.523 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.655 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.374 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.335 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.391 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.308 |
LIG_LIR_Apic_2 | 502 | 507 | PF02991 | 0.358 |
LIG_LIR_Apic_2 | 88 | 94 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 250 | 260 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 362 | 371 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 481 | 492 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 710 | 721 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 481 | 487 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 710 | 716 | PF02991 | 0.288 |
LIG_PCNA_PIPBox_1 | 569 | 578 | PF02747 | 0.391 |
LIG_PTB_Apo_2 | 264 | 271 | PF02174 | 0.294 |
LIG_PTB_Phospho_1 | 264 | 270 | PF10480 | 0.255 |
LIG_SH2_CRK | 539 | 543 | PF00017 | 0.275 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 717 | 721 | PF00017 | 0.306 |
LIG_SH2_PTP2 | 713 | 716 | PF00017 | 0.298 |
LIG_SH2_SRC | 83 | 86 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 717 | 721 | PF00017 | 0.323 |
LIG_SH2_STAT3 | 673 | 676 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.207 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.663 |
LIG_SH3_2 | 144 | 149 | PF14604 | 0.596 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.648 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.696 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.565 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 315 | 321 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 54 | 60 | PF11976 | 0.516 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.249 |
LIG_TYR_ITIM | 715 | 720 | PF00017 | 0.298 |
LIG_UBA3_1 | 316 | 322 | PF00899 | 0.275 |
LIG_UBA3_1 | 541 | 546 | PF00899 | 0.270 |
MOD_CDC14_SPxK_1 | 146 | 149 | PF00782 | 0.597 |
MOD_CDK_SPxK_1 | 143 | 149 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 94 | 100 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 143 | 150 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.424 |
MOD_CDK_SPxxK_3 | 60 | 67 | PF00069 | 0.562 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.666 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.686 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.596 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.613 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.453 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.628 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.674 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.561 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.368 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.401 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.597 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.665 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.583 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.305 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.370 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.635 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.629 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.720 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.308 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.386 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.375 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.377 |
MOD_CK2_1 | 685 | 691 | PF00069 | 0.310 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.744 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.645 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.724 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.632 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.654 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.445 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.280 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.341 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.667 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.375 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.396 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.387 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.330 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.630 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.666 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.610 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.528 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.462 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.608 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.539 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.568 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.708 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.650 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.428 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.308 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.291 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.734 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.373 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.316 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.399 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.414 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.718 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.540 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.591 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.583 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.502 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.585 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.391 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.333 |
MOD_N-GLC_1 | 608 | 613 | PF02516 | 0.475 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.306 |
MOD_N-GLC_2 | 267 | 269 | PF02516 | 0.294 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.594 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.770 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.496 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.439 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.737 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.492 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.377 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.374 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.347 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.216 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.281 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.715 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.544 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.275 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.373 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.564 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.716 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.690 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.720 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.335 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.516 |
MOD_PKA_1 | 397 | 403 | PF00069 | 0.374 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.646 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.491 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.289 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.365 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.428 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.294 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.474 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.324 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.562 |
MOD_Plk_2-3 | 574 | 580 | PF00069 | 0.391 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.391 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.275 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.282 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.298 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.641 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.542 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.660 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.614 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.440 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.586 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.569 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.558 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.658 |
MOD_ProDKin_1 | 452 | 458 | PF00069 | 0.298 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.684 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.547 |
MOD_SUMO_for_1 | 347 | 350 | PF00179 | 0.264 |
MOD_SUMO_for_1 | 389 | 392 | PF00179 | 0.264 |
MOD_SUMO_rev_2 | 519 | 524 | PF00179 | 0.445 |
MOD_SUMO_rev_2 | 79 | 89 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_2 | 361 | 367 | PF01217 | 0.275 |
TRG_DiLeu_BaEn_2 | 649 | 655 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 713 | 716 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 717 | 720 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 635 | 637 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.391 |
TRG_NLS_MonoExtN_4 | 636 | 641 | PF00514 | 0.296 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Z2 | Leptomonas seymouri | 24% | 90% |
A0A0N0P852 | Leptomonas seymouri | 63% | 95% |
A0A3Q8IB18 | Leishmania donovani | 99% | 100% |
A0A422MZT5 | Trypanosoma rangeli | 41% | 100% |
A4HBN8 | Leishmania braziliensis | 74% | 99% |
A4HDC0 | Leishmania braziliensis | 22% | 89% |
A4IBF1 | Leishmania infantum | 24% | 100% |
D0A1P0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AV07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QAS1 | Leishmania major | 22% | 89% |
Q4QCH5 | Leishmania major | 95% | 100% |
V5DGZ8 | Trypanosoma cruzi | 40% | 100% |