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 | yes | yes: 8, no: 2 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q0L6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.669 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.588 |
CLV_PCSK_FUR_1 | 137 | 141 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 380 | 382 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.660 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.659 |
DOC_CYCLIN_RxL_1 | 235 | 246 | PF00134 | 0.632 |
DOC_CYCLIN_yClb1_LxF_4 | 262 | 268 | PF00134 | 0.476 |
DOC_MAPK_MEF2A_6 | 13 | 20 | PF00069 | 0.570 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.496 |
DOC_PP2B_LxvP_1 | 242 | 245 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.654 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.594 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 103 | 110 | PF00244 | 0.715 |
LIG_14-3-3_CanoR_1 | 184 | 194 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 381 | 387 | PF00244 | 0.523 |
LIG_BIR_III_4 | 98 | 102 | PF00653 | 0.520 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.519 |
LIG_deltaCOP1_diTrp_1 | 129 | 133 | PF00928 | 0.574 |
LIG_deltaCOP1_diTrp_1 | 358 | 367 | PF00928 | 0.448 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.596 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.640 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.473 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.576 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.689 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.498 |
LIG_GBD_Chelix_1 | 15 | 23 | PF00786 | 0.504 |
LIG_LIR_Apic_2 | 54 | 60 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 325 | 334 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.526 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.575 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.469 |
LIG_Pex14_1 | 313 | 317 | PF04695 | 0.341 |
LIG_PTB_Apo_2 | 281 | 288 | PF02174 | 0.555 |
LIG_PTB_Apo_2 | 304 | 311 | PF02174 | 0.460 |
LIG_PTB_Phospho_1 | 281 | 287 | PF10480 | 0.553 |
LIG_PTB_Phospho_1 | 304 | 310 | PF10480 | 0.457 |
LIG_RPA_C_Fungi | 173 | 185 | PF08784 | 0.578 |
LIG_SH2_CRK | 287 | 291 | PF00017 | 0.529 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.690 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.552 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.572 |
LIG_SH2_NCK_1 | 57 | 61 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.552 |
LIG_SH2_STAT3 | 231 | 234 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.523 |
LIG_SH3_2 | 244 | 249 | PF14604 | 0.619 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.561 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 14 | 20 | PF11976 | 0.507 |
LIG_SUMO_SIM_anti_2 | 39 | 44 | PF11976 | 0.462 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.638 |
LIG_TRFH_1 | 222 | 226 | PF08558 | 0.418 |
LIG_Vh1_VBS_1 | 7 | 25 | PF01044 | 0.424 |
LIG_WRC_WIRS_1 | 411 | 416 | PF05994 | 0.562 |
MOD_CDC14_SPxK_1 | 246 | 249 | PF00782 | 0.670 |
MOD_CDK_SPK_2 | 347 | 352 | PF00069 | 0.511 |
MOD_CDK_SPxK_1 | 243 | 249 | PF00069 | 0.645 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.628 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.476 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.633 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.538 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.762 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.587 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.684 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.544 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.442 |
MOD_CMANNOS | 130 | 133 | PF00535 | 0.573 |
MOD_CMANNOS | 313 | 316 | PF00535 | 0.466 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.489 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.625 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.526 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.485 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.446 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.658 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.636 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.603 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.653 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.667 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.568 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.676 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.447 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.435 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.560 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.588 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.533 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.669 |
MOD_N-GLC_1 | 375 | 380 | PF02516 | 0.628 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.570 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.701 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.543 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.602 |
MOD_NEK2_2 | 89 | 94 | PF00069 | 0.756 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.703 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.464 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.585 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.749 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.552 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.442 |
MOD_PKB_1 | 366 | 374 | PF00069 | 0.559 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.690 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.502 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.447 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.588 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.568 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.406 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.601 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.653 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.630 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.665 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.594 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.739 |
TRG_DiLeu_BaEn_1 | 154 | 159 | PF01217 | 0.614 |
TRG_DiLeu_BaEn_4 | 154 | 160 | PF01217 | 0.606 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.689 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.585 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 205 | 210 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 390 | 394 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.365 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P921 | Leptomonas seymouri | 57% | 100% |
A0A0S4JQR0 | Bodo saltans | 23% | 100% |
A0A1X0P090 | Trypanosomatidae | 29% | 100% |
A0A3Q8IRP6 | Leishmania donovani | 92% | 100% |
A0A422NKF7 | Trypanosoma rangeli | 32% | 100% |
A4HQ60 | Leishmania braziliensis | 76% | 98% |
A4IDV9 | Leishmania infantum | 92% | 100% |
D0A457 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ATY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |