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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B621
Term | Name | Level | Count |
---|---|---|---|
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016560 | protein import into peroxisome matrix, docking | 5 | 1 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0006810 | transport | 3 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000268 | peroxisome targeting sequence binding | 5 | 1 |
GO:0005048 | signal sequence binding | 4 | 1 |
GO:0005052 | peroxisome matrix targeting signal-1 binding | 6 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0042277 | peptide binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.324 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.316 |
DEG_APCC_DBOX_1 | 594 | 602 | PF00400 | 0.305 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.523 |
DOC_MAPK_DCC_7 | 152 | 161 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 152 | 161 | PF00069 | 0.505 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.471 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.637 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.508 |
DOC_PP4_FxxP_1 | 450 | 453 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.207 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.466 |
DOC_USP7_UBL2_3 | 509 | 513 | PF12436 | 0.293 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 595 | 599 | PF00244 | 0.328 |
LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.442 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.396 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.477 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.646 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.304 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.500 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.414 |
LIG_FXI_DFP_1 | 326 | 330 | PF00024 | 0.377 |
LIG_IBAR_NPY_1 | 322 | 324 | PF08397 | 0.326 |
LIG_LIR_Apic_2 | 188 | 192 | PF02991 | 0.639 |
LIG_LIR_Apic_2 | 259 | 265 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 447 | 453 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 299 | 307 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 361 | 372 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 427 | 436 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.487 |
LIG_Pex14_1 | 179 | 183 | PF04695 | 0.511 |
LIG_Pex14_1 | 296 | 300 | PF04695 | 0.474 |
LIG_Pex14_1 | 53 | 57 | PF04695 | 0.467 |
LIG_Pex14_2 | 618 | 622 | PF04695 | 0.308 |
LIG_PTB_Apo_2 | 535 | 542 | PF02174 | 0.234 |
LIG_PTB_Phospho_1 | 535 | 541 | PF10480 | 0.234 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.609 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.650 |
LIG_SH2_GRB2like | 552 | 555 | PF00017 | 0.308 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.539 |
LIG_SH2_NCK_1 | 558 | 562 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 463 | 467 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 558 | 562 | PF00017 | 0.208 |
LIG_SH2_STAT3 | 611 | 614 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.257 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.469 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.493 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.524 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.383 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.443 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.468 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 377 | 383 | PF11976 | 0.324 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.475 |
LIG_TYR_ITSM | 179 | 186 | PF00017 | 0.646 |
LIG_UBA3_1 | 381 | 389 | PF00899 | 0.423 |
LIG_WRC_WIRS_1 | 186 | 191 | PF05994 | 0.635 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.555 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.542 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.426 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.483 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.747 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.398 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.254 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.443 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.485 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.640 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.602 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.531 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.671 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.621 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.624 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.513 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.569 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.617 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.735 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.588 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.473 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.440 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.376 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.440 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.452 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.660 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.408 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.411 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.577 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.312 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.307 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.234 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.327 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.512 |
MOD_NEK2_2 | 414 | 419 | PF00069 | 0.354 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.640 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.678 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.647 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.651 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.309 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.380 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.402 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.338 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.699 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.328 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.697 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.599 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.426 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.412 |
MOD_Plk_2-3 | 195 | 201 | PF00069 | 0.560 |
MOD_Plk_2-3 | 458 | 464 | PF00069 | 0.530 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.686 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.580 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.395 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.549 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.450 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.585 |
MOD_SUMO_for_1 | 622 | 625 | PF00179 | 0.225 |
MOD_SUMO_rev_2 | 190 | 199 | PF00179 | 0.614 |
MOD_SUMO_rev_2 | 506 | 510 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 616 | 624 | PF00179 | 0.333 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_1 | 32 | 37 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_2 | 206 | 212 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.723 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.308 |
TRG_NES_CRM1_1 | 613 | 625 | PF08389 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT5 | Leptomonas seymouri | 81% | 100% |
A0A0S4KFV0 | Bodo saltans | 46% | 100% |
A0A1X0NH73 | Trypanosomatidae | 51% | 96% |
A0A3S7X906 | Leishmania donovani | 95% | 100% |
A0A422N9P3 | Trypanosoma rangeli | 58% | 96% |
A4HMG4 | Leishmania braziliensis | 85% | 100% |
A4IB35 | Leishmania infantum | 95% | 100% |
C9ZNN6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 96% |
E9AEW5 | Leishmania major | 93% | 100% |
O70525 | Cavia porcellus | 32% | 98% |
Q9FMA3 | Arabidopsis thaliana | 34% | 86% |
V5B7T1 | Trypanosoma cruzi | 48% | 94% |