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: A4HNG8
Term | Name | Level | Count |
---|---|---|---|
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: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:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 290 | 294 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 297 | 301 | PF00656 | 0.594 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.323 |
CLV_PCSK_FUR_1 | 138 | 142 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 41 | 49 | PF00400 | 0.525 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.536 |
DEG_SPOP_SBC_1 | 192 | 196 | PF00917 | 0.553 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.569 |
DOC_MAPK_gen_1 | 466 | 474 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 475 | 484 | PF00069 | 0.508 |
DOC_MAPK_RevD_3 | 454 | 467 | PF00069 | 0.475 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.550 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.645 |
DOC_USP7_UBL2_3 | 136 | 140 | PF12436 | 0.544 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 211 | 220 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 254 | 261 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 346 | 355 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 448 | 458 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 481 | 491 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 3 | 20 | PF00022 | 0.289 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 85 | 89 | PF00533 | 0.671 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.523 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.486 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.376 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.513 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.761 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.508 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.432 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.806 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.471 |
LIG_LIR_Apic_2 | 240 | 244 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 173 | 181 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 350 | 357 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 401 | 409 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 452 | 461 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 490 | 498 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 350 | 356 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 436 | 440 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.453 |
LIG_PDZ_Class_3 | 509 | 514 | PF00595 | 0.320 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.671 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.357 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.440 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 402 | 406 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.390 |
LIG_SH3_1 | 18 | 24 | PF00018 | 0.356 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.369 |
LIG_SUMO_SIM_par_1 | 235 | 240 | PF11976 | 0.246 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.535 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.453 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.638 |
LIG_TRAF2_2 | 471 | 476 | PF00917 | 0.492 |
LIG_TRFH_1 | 454 | 458 | PF08558 | 0.409 |
MOD_CDC14_SPxK_1 | 285 | 288 | PF00782 | 0.470 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.573 |
MOD_CDK_SPxK_1 | 282 | 288 | PF00069 | 0.469 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.641 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.440 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.721 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.687 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.285 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.338 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.454 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.659 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.388 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.489 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.390 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.749 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.295 |
MOD_Cter_Amidation | 138 | 141 | PF01082 | 0.807 |
MOD_Cter_Amidation | 464 | 467 | PF01082 | 0.324 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.743 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.650 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.445 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.488 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.290 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.595 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.579 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.436 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.541 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.642 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.478 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.395 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.684 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.621 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.295 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.321 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.479 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.700 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.520 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.392 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.297 |
MOD_PKA_1 | 8 | 14 | PF00069 | 0.272 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.432 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.185 |
MOD_PKB_1 | 344 | 352 | PF00069 | 0.440 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.320 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.293 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.684 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.330 |
MOD_Plk_2-3 | 216 | 222 | PF00069 | 0.317 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.356 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.447 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.595 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.529 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.662 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.573 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.194 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.312 |
MOD_SUMO_for_1 | 278 | 281 | PF00179 | 0.607 |
MOD_SUMO_rev_2 | 4 | 11 | PF00179 | 0.427 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.277 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.293 |
TRG_NLS_Bipartite_1 | 126 | 141 | PF00514 | 0.776 |
TRG_NLS_MonoExtC_3 | 135 | 140 | PF00514 | 0.589 |
TRG_NLS_MonoExtN_4 | 136 | 141 | PF00514 | 0.754 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGL8 | Leptomonas seymouri | 59% | 99% |
A0A1X0P4S2 | Trypanosomatidae | 39% | 100% |
A0A3Q8IQ93 | Leishmania donovani | 73% | 100% |
A0A3S5IQY8 | Trypanosoma rangeli | 38% | 99% |
A4IC59 | Leishmania infantum | 74% | 100% |
C9ZYE4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AFX9 | Leishmania major | 74% | 100% |
E9B732 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
V5DQH4 | Trypanosoma cruzi | 41% | 100% |