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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X0F2
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0042026 | protein refolding | 3 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.744 |
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.618 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 230 | 234 | PF00082 | 0.398 |
CLV_PCSK_FUR_1 | 366 | 370 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.353 |
CLV_PCSK_PC7_1 | 369 | 375 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.506 |
DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.345 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.633 |
DOC_CKS1_1 | 16 | 21 | PF01111 | 0.328 |
DOC_CYCLIN_RxL_1 | 193 | 202 | PF00134 | 0.505 |
DOC_CYCLIN_RxL_1 | 99 | 111 | PF00134 | 0.558 |
DOC_MAPK_gen_1 | 31 | 39 | PF00069 | 0.176 |
DOC_PP1_RVXF_1 | 31 | 37 | PF00149 | 0.439 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.744 |
DOC_SPAK_OSR1_1 | 369 | 373 | PF12202 | 0.696 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.680 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.497 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 131 | 137 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.644 |
LIG_BRCT_BRCA1_1 | 125 | 129 | PF00533 | 0.716 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 2 | 6 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.775 |
LIG_BRCT_BRCA1_1 | 408 | 412 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.428 |
LIG_EVH1_1 | 15 | 19 | PF00568 | 0.324 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.682 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.371 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.560 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.684 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.670 |
LIG_LIR_Apic_2 | 409 | 415 | PF02991 | 0.747 |
LIG_LIR_Gen_1 | 176 | 185 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 21 | 30 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 21 | 25 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.719 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.544 |
LIG_NRBOX | 446 | 452 | PF00104 | 0.438 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.763 |
LIG_Pex14_2 | 290 | 294 | PF04695 | 0.588 |
LIG_Pex14_2 | 335 | 339 | PF04695 | 0.695 |
LIG_PTB_Apo_2 | 70 | 77 | PF02174 | 0.534 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.480 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.345 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 224 | 228 | PF00017 | 0.525 |
LIG_SH2_PTP2 | 178 | 181 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 81 | 84 | PF00017 | 0.577 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.706 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.169 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.705 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.577 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.322 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.531 |
LIG_SUMO_SIM_anti_2 | 467 | 473 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.438 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.626 |
LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.419 |
LIG_WRPW_2 | 335 | 338 | PF00400 | 0.634 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.674 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.513 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.656 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.357 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.525 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.646 |
MOD_Cter_Amidation | 366 | 369 | PF01082 | 0.705 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.675 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.691 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.430 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.703 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.576 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.668 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.391 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.727 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.486 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.652 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.649 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.626 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.425 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.434 |
MOD_N-GLC_1 | 380 | 385 | PF02516 | 0.603 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.661 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.704 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.694 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.616 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.519 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.397 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.181 |
MOD_NEK2_2 | 123 | 128 | PF00069 | 0.594 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.422 |
MOD_PIKK_1 | 407 | 413 | PF00454 | 0.716 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.639 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.440 |
MOD_PK_1 | 216 | 222 | PF00069 | 0.492 |
MOD_PKA_1 | 368 | 374 | PF00069 | 0.650 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.687 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.603 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.535 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.444 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.537 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.635 |
MOD_Plk_2-3 | 358 | 364 | PF00069 | 0.603 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.357 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.357 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.357 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.478 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.396 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.594 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.433 |
MOD_SUMO_rev_2 | 186 | 195 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_4 | 307 | 313 | PF01217 | 0.601 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.747 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.478 |
TRG_NES_CRM1_1 | 287 | 300 | PF08389 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD75 | Leptomonas seymouri | 70% | 100% |
A0A0S4JV26 | Bodo saltans | 41% | 100% |
A4HFG5 | Leishmania braziliensis | 82% | 100% |
A4I2M7 | Leishmania infantum | 100% | 100% |
E9AD18 | Leishmania major | 95% | 100% |
E9AYU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BN28 | Trypanosoma cruzi | 48% | 100% |