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. | yes | yes: 20 |
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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005840 | ribosome | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AHX6
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0031386 | protein tag | 1 | 1 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 1 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 1 |
GO:0003735 | structural constituent of ribosome | 2 | 1 |
GO:0005198 | structural molecule activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 538 | 542 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.320 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.270 |
DOC_MAPK_gen_1 | 148 | 157 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 224 | 233 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 300 | 309 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 452 | 461 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 528 | 537 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 604 | 613 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 72 | 81 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 145 | 157 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 221 | 233 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 297 | 309 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 373 | 385 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 449 | 461 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 525 | 537 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 601 | 613 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 69 | 81 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 139 | 147 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 148 | 157 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 215 | 223 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 224 | 233 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 291 | 299 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 367 | 375 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 376 | 385 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 443 | 451 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 452 | 461 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 519 | 527 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 528 | 537 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 595 | 603 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 604 | 613 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 63 | 71 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 671 | 679 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 116 | 122 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 192 | 198 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 268 | 274 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 344 | 350 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 40 | 46 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 420 | 426 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 496 | 502 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 572 | 578 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 648 | 654 | PF00149 | 0.520 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 181 | 185 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 257 | 261 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 29 | 33 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 333 | 337 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 409 | 413 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 561 | 565 | PF12436 | 0.520 |
DOC_USP7_UBL2_3 | 637 | 641 | PF12436 | 0.520 |
LIG_14-3-3_CanoR_1 | 130 | 137 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 206 | 213 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 282 | 289 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 358 | 365 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 434 | 441 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 510 | 517 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 54 | 61 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 586 | 593 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 662 | 669 | PF00244 | 0.520 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.520 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.533 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.520 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.520 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.520 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.520 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.553 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.520 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.520 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.520 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.520 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.520 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.520 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.520 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.520 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.520 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.520 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.520 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.520 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.558 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.604 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.520 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.520 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.520 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.520 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.574 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.520 |
LIG_GBD_Chelix_1 | 145 | 153 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 221 | 229 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 297 | 305 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 373 | 381 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 449 | 457 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 525 | 533 | PF00786 | 0.320 |
LIG_GBD_Chelix_1 | 601 | 609 | PF00786 | 0.320 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.374 |
LIG_SH2_STAT3 | 135 | 138 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 211 | 214 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 287 | 290 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 515 | 518 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 591 | 594 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 667 | 670 | PF00017 | 0.520 |
LIG_SUMO_SIM_par_1 | 11 | 16 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 163 | 168 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 239 | 244 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 315 | 320 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 391 | 396 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 467 | 472 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 543 | 548 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 619 | 624 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 87 | 92 | PF11976 | 0.520 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.558 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.520 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.574 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.520 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.520 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.520 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.520 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.520 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.520 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.579 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.520 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.520 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.520 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.520 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.520 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.520 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.520 |
MOD_Plk_1 | 671 | 677 | PF00069 | 0.520 |
MOD_Plk_2-3 | 128 | 134 | PF00069 | 0.520 |
MOD_Plk_2-3 | 204 | 210 | PF00069 | 0.520 |
MOD_Plk_2-3 | 280 | 286 | PF00069 | 0.520 |
MOD_Plk_2-3 | 356 | 362 | PF00069 | 0.520 |
MOD_Plk_2-3 | 432 | 438 | PF00069 | 0.520 |
MOD_Plk_2-3 | 508 | 514 | PF00069 | 0.520 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.520 |
MOD_Plk_2-3 | 584 | 590 | PF00069 | 0.520 |
MOD_Plk_2-3 | 660 | 666 | PF00069 | 0.520 |
TRG_DiLeu_BaEn_4 | 127 | 133 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 203 | 209 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 279 | 285 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 355 | 361 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 431 | 437 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 507 | 513 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 51 | 57 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 583 | 589 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 659 | 665 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 191 | 196 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 267 | 272 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 343 | 348 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 495 | 500 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 571 | 576 | PF01217 | 0.520 |
TRG_DiLeu_BaLyEn_6 | 647 | 652 | PF01217 | 0.520 |
TRG_ER_diArg_1 | 147 | 150 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 282 | 286 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 352 | 356 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 428 | 432 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 48 | 52 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 504 | 508 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 510 | 514 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 54 | 58 | PF00026 | 0.245 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 586 | 590 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 656 | 660 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.270 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HPM0 | Leishmania braziliensis | 99% | 100% |
A4HU11 | Leishmania infantum | 100% | 100% |
P0CG48 | Homo sapiens | 97% | 100% |
P0CG50 | Mus musculus | 97% | 93% |
P0CG61 | Pongo pygmaeus | 97% | 90% |
P0CG64 | Pan troglodytes | 97% | 90% |
P0CG66 | Gorilla gorilla gorilla | 97% | 100% |
P0CG68 | Sus scrofa | 97% | 100% |
P0CG69 | Drosophila melanogaster | 97% | 90% |
P0CG71 | Caenorhabditis elegans | 96% | 82% |
P0CG78 | Dictyostelium discoideum | 95% | 100% |
P0CG85 | Nicotiana sylvestris | 93% | 100% |
P0CH04 | Petroselinum crispum | 93% | 100% |
P0CH05 | Petroselinum crispum | 93% | 100% |
P0CH28 | Bos taurus | 97% | 99% |
P42740 | Aglaothamnion neglectum | 94% | 100% |
P59669 | Geodia cydonium | 96% | 100% |
P62976 | Cricetulus griseus | 96% | 100% |
Q39256 | Arabidopsis thaliana | 72% | 100% |
Q4Q165 | Leishmania major | 100% | 100% |
Q63429 | Rattus norvegicus | 97% | 84% |
Q8H159 | Arabidopsis thaliana | 93% | 100% |