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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005778 | peroxisomal membrane | 6 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 3 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031903 | microbody membrane | 5 | 2 |
GO:0042579 | microbody | 5 | 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:0046860 | glycosome membrane | 7 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QDL4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007031 | peroxisome organization | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015919 | peroxisomal membrane transport | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0043574 | peroxisomal transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.344 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.634 |
CLV_PCSK_FUR_1 | 321 | 325 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.527 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.361 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.557 |
DEG_SPOP_SBC_1 | 31 | 35 | PF00917 | 0.217 |
DOC_CYCLIN_yCln2_LP_2 | 38 | 44 | PF00134 | 0.351 |
DOC_MAPK_gen_1 | 195 | 205 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 290 | 298 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 5 | 12 | PF00069 | 0.532 |
DOC_MAPK_MEF2A_6 | 292 | 300 | PF00069 | 0.343 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.543 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 238 | 248 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 347 | 355 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.534 |
LIG_Actin_WH2_1 | 202 | 220 | PF00022 | 0.311 |
LIG_Actin_WH2_2 | 205 | 220 | PF00022 | 0.412 |
LIG_BIR_III_4 | 331 | 335 | PF00653 | 0.728 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.217 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.195 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.556 |
LIG_DLG_GKlike_1 | 246 | 254 | PF00625 | 0.394 |
LIG_eIF4E_1 | 83 | 89 | PF01652 | 0.574 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.401 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.521 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.217 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.568 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.751 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.755 |
LIG_GBD_Chelix_1 | 205 | 213 | PF00786 | 0.659 |
LIG_IBAR_NPY_1 | 107 | 109 | PF08397 | 0.489 |
LIG_LIR_Apic_2 | 403 | 407 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 33 | 44 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.184 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.561 |
LIG_PDZ_Class_1 | 461 | 466 | PF00595 | 0.654 |
LIG_Pex14_1 | 370 | 374 | PF04695 | 0.742 |
LIG_Pex14_2 | 224 | 228 | PF04695 | 0.376 |
LIG_PTB_Apo_2 | 103 | 110 | PF02174 | 0.451 |
LIG_PTB_Phospho_1 | 103 | 109 | PF10480 | 0.422 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.766 |
LIG_SH2_CRK | 404 | 408 | PF00017 | 0.507 |
LIG_SH2_SRC | 427 | 430 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.732 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.561 |
LIG_SH2_STAT3 | 402 | 405 | PF00017 | 0.561 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.480 |
LIG_TRAF2_1 | 242 | 245 | PF00917 | 0.346 |
LIG_TYR_ITIM | 22 | 27 | PF00017 | 0.217 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.702 |
MOD_CDK_SPxxK_3 | 165 | 172 | PF00069 | 0.617 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.735 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.692 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.604 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.410 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.697 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.610 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.400 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.402 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.591 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.463 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.407 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.647 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.656 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.622 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.436 |
MOD_CMANNOS | 291 | 294 | PF00535 | 0.511 |
MOD_Cter_Amidation | 446 | 449 | PF01082 | 0.422 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.494 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.559 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.646 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.573 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.693 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.547 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.731 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.662 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.671 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.621 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.585 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.217 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.629 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.665 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.762 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.636 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.571 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.800 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.217 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.524 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.684 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.687 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.741 |
MOD_PIKK_1 | 264 | 270 | PF00454 | 0.716 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.716 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.742 |
MOD_PKA_1 | 323 | 329 | PF00069 | 0.591 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.405 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.620 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.668 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.750 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.624 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.411 |
MOD_PKB_1 | 321 | 329 | PF00069 | 0.596 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.762 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.635 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.676 |
MOD_Plk_2-3 | 362 | 368 | PF00069 | 0.632 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.631 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.489 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.552 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.609 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.746 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.505 |
MOD_SUMO_rev_2 | 8 | 18 | PF00179 | 0.387 |
TRG_DiLeu_BaEn_3 | 13 | 19 | PF01217 | 0.380 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.734 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 321 | 324 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.430 |
TRG_NES_CRM1_1 | 204 | 215 | PF08389 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.624 |
TRG_PTS1 | 463 | 466 | PF00515 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9X6 | Leptomonas seymouri | 70% | 100% |
A0A0S4J170 | Bodo saltans | 26% | 100% |
A0A1X0P6F7 | Trypanosomatidae | 36% | 100% |
A0A3S7WV91 | Leishmania donovani | 88% | 100% |
A0A422NCY3 | Trypanosoma rangeli | 31% | 100% |
A4H9W4 | Leishmania braziliensis | 78% | 100% |
E9AGQ9 | Leishmania infantum | 90% | 100% |
E9ARV8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |