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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: Q4QIE3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.660 |
CLV_PCSK_FUR_1 | 142 | 146 | PF00082 | 0.562 |
CLV_PCSK_FUR_1 | 328 | 332 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.775 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.617 |
DEG_APCC_DBOX_1 | 159 | 167 | PF00400 | 0.561 |
DEG_APCC_DBOX_1 | 27 | 35 | PF00400 | 0.657 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.668 |
DEG_SCF_FBW7_1 | 279 | 284 | PF00400 | 0.535 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.630 |
DOC_ANK_TNKS_1 | 425 | 432 | PF00023 | 0.465 |
DOC_CYCLIN_RxL_1 | 408 | 419 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 408 | 418 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 301 | 304 | PF13499 | 0.659 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.637 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.705 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 195 | 203 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 267 | 274 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 333 | 338 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 49 | 58 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 90 | 97 | PF00244 | 0.706 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.657 |
LIG_Clathr_ClatBox_1 | 415 | 419 | PF01394 | 0.500 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.654 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.660 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.532 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.639 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.581 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.544 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.651 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.497 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.452 |
LIG_NRBOX | 411 | 417 | PF00104 | 0.511 |
LIG_PDZ_Class_2 | 433 | 438 | PF00595 | 0.533 |
LIG_RPA_C_Fungi | 334 | 346 | PF08784 | 0.542 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.530 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.531 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.664 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.648 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.702 |
LIG_SUMO_SIM_par_1 | 414 | 419 | PF11976 | 0.505 |
LIG_WRPW_2 | 107 | 110 | PF00400 | 0.562 |
LIG_WW_3 | 235 | 239 | PF00397 | 0.668 |
LIG_WW_3 | 245 | 249 | PF00397 | 0.551 |
LIG_WW_3 | 264 | 268 | PF00397 | 0.501 |
LIG_WW_3 | 303 | 307 | PF00397 | 0.644 |
MOD_CDC14_SPxK_1 | 8 | 11 | PF00782 | 0.661 |
MOD_CDK_SPxK_1 | 5 | 11 | PF00069 | 0.660 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.668 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.564 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.615 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.790 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.825 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.578 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.520 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.730 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.638 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.579 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.674 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.536 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.495 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.668 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.740 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.592 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.721 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.664 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.753 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.743 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.659 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.646 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.618 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.518 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.666 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.624 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.680 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.544 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.742 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.729 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.675 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.601 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.553 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.661 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.570 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.613 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.689 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.610 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.606 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.761 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.705 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.492 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.546 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.582 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.682 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.644 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.722 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.505 |
MOD_PKB_1 | 331 | 339 | PF00069 | 0.593 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.505 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.666 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.541 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.690 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.568 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.608 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.636 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.640 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.687 |
MOD_SUMO_rev_2 | 168 | 175 | PF00179 | 0.500 |
TRG_DiLeu_BaEn_1 | 27 | 32 | PF01217 | 0.655 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.646 |
TRG_NLS_Bipartite_1 | 328 | 348 | PF00514 | 0.547 |
TRG_NLS_MonoCore_2 | 343 | 348 | PF00514 | 0.561 |
TRG_NLS_MonoExtC_3 | 343 | 348 | PF00514 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 414 | 419 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H638 | Leishmania donovani | 89% | 100% |
A4HTH7 | Leishmania infantum | 89% | 100% |
E9AMA5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |