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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9AFX9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010033 | response to organic substance | 3 | 2 |
GO:0010243 | response to organonitrogen compound | 4 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 2 |
GO:0036503 | ERAD pathway | 5 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901698 | response to nitrogen compound | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.693 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.323 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.240 |
DEG_APCC_DBOX_1 | 41 | 49 | PF00400 | 0.520 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.565 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.545 |
DEG_SCF_FBW7_1 | 17 | 24 | PF00400 | 0.446 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.606 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.759 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.540 |
DOC_CKS1_1 | 204 | 209 | PF01111 | 0.392 |
DOC_CYCLIN_RxL_1 | 9 | 20 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.516 |
DOC_MAPK_DCC_7 | 468 | 476 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 468 | 476 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 477 | 486 | PF00069 | 0.508 |
DOC_MAPK_RevD_3 | 456 | 469 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 208 | 214 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.591 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.650 |
DOC_USP7_UBL2_3 | 124 | 128 | PF12436 | 0.660 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.543 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 22 | 26 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 450 | 460 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 483 | 493 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 505 | 509 | PF00244 | 0.583 |
LIG_14-3-3_CterR_2 | 519 | 522 | PF00244 | 0.501 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.571 |
LIG_BRCT_BRCA1_1 | 85 | 89 | PF00533 | 0.679 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.586 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.443 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.543 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.531 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.521 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.525 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.508 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.770 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.406 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.482 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.613 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.666 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.552 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.471 |
LIG_LIR_Gen_1 | 171 | 181 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 352 | 359 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 403 | 411 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 492 | 500 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 403 | 407 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 429 | 433 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 438 | 442 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.453 |
LIG_NRBOX | 13 | 19 | PF00104 | 0.389 |
LIG_PCNA_yPIPBox_3 | 199 | 212 | PF02747 | 0.513 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.679 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.376 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.440 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.516 |
LIG_SH2_NCK_1 | 404 | 408 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 442 | 446 | PF00017 | 0.535 |
LIG_SH2_STAT3 | 510 | 513 | PF00017 | 0.487 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.391 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.451 |
LIG_TRAF2_1 | 323 | 326 | PF00917 | 0.623 |
LIG_TRAF2_1 | 413 | 416 | PF00917 | 0.535 |
LIG_TRAF2_1 | 492 | 495 | PF00917 | 0.453 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.634 |
LIG_TRAF2_2 | 473 | 478 | PF00917 | 0.492 |
LIG_TRFH_1 | 456 | 460 | PF08558 | 0.535 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.540 |
MOD_CDK_SPK_2 | 281 | 286 | PF00069 | 0.636 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.544 |
MOD_CDK_SPxxK_3 | 203 | 210 | PF00069 | 0.385 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.638 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.716 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.765 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.446 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.498 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.463 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.756 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.624 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.363 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.406 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.716 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.453 |
MOD_Cter_Amidation | 466 | 469 | PF01082 | 0.275 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.694 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.591 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.762 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.435 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.521 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.688 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.436 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.535 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.742 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.453 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.346 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.411 |
MOD_PIKK_1 | 406 | 412 | PF00454 | 0.455 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.704 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.488 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.538 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.552 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.375 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.560 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.655 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.560 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.479 |
MOD_Plk_2-3 | 138 | 144 | PF00069 | 0.552 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.635 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.465 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.682 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.497 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.575 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.732 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.501 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.380 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.706 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.465 |
MOD_SUMO_for_1 | 198 | 201 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 4 | 11 | PF00179 | 0.428 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGL8 | Leptomonas seymouri | 63% | 100% |
A0A1X0P4S2 | Trypanosomatidae | 42% | 100% |
A0A3Q8IQ93 | Leishmania donovani | 91% | 100% |
A0A3S5IQY8 | Trypanosoma rangeli | 39% | 100% |
A4HNG8 | Leishmania braziliensis | 74% | 100% |
A4IC59 | Leishmania infantum | 92% | 100% |
C9ZYE4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9B732 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5DQH4 | Trypanosoma cruzi | 42% | 100% |