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 |
Related structures:
AlphaFold database: E9AHY4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.594 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.646 |
CLV_PCSK_FUR_1 | 384 | 388 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.645 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 384 | 390 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.508 |
DEG_APCC_DBOX_1 | 177 | 185 | PF00400 | 0.463 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.533 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.478 |
DEG_SCF_FBW7_2 | 35 | 42 | PF00400 | 0.544 |
DEG_SPOP_SBC_1 | 200 | 204 | PF00917 | 0.649 |
DOC_CYCLIN_RxL_1 | 264 | 271 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 142 | 149 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.470 |
DOC_PP2B_LxvP_1 | 227 | 230 | PF13499 | 0.555 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.506 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.585 |
DOC_USP7_UBL2_3 | 377 | 381 | PF12436 | 0.722 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.461 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 186 | 194 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.544 |
LIG_Actin_WH2_2 | 406 | 424 | PF00022 | 0.513 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.670 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.399 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.680 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.599 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.543 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.501 |
LIG_LYPXL_SIV_4 | 300 | 308 | PF13949 | 0.484 |
LIG_NBox_RRM_1 | 331 | 341 | PF00076 | 0.454 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.537 |
LIG_NRBOX | 340 | 346 | PF00104 | 0.477 |
LIG_PCNA_yPIPBox_3 | 425 | 439 | PF02747 | 0.355 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.578 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.519 |
LIG_SUMO_SIM_anti_2 | 121 | 126 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.504 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.537 |
LIG_TYR_ITIM | 15 | 20 | PF00017 | 0.569 |
MOD_CDC14_SPxK_1 | 130 | 133 | PF00782 | 0.546 |
MOD_CDK_SPxK_1 | 127 | 133 | PF00069 | 0.549 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.648 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.682 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.615 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.610 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.448 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.417 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.504 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.646 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.478 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.626 |
MOD_Cter_Amidation | 384 | 387 | PF01082 | 0.667 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.645 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.719 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.698 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.468 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.489 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.545 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.698 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.361 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.606 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.673 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.644 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.538 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.589 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.648 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.584 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.609 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.668 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.702 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.370 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.714 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.516 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.448 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.619 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.605 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.482 |
MOD_PK_1 | 120 | 126 | PF00069 | 0.533 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.559 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.538 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.428 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.749 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.546 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.569 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.554 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.687 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.623 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.428 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.538 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.632 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.539 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.701 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.688 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.450 |
MOD_SUMO_rev_2 | 368 | 376 | PF00179 | 0.596 |
TRG_DiLeu_BaEn_1 | 419 | 424 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEF3 | Leptomonas seymouri | 45% | 84% |
A0A1X0NLI7 | Trypanosomatidae | 29% | 100% |
A0A3Q8IPS4 | Leishmania donovani | 100% | 100% |
A0A3R7NLX1 | Trypanosoma rangeli | 27% | 100% |
A4HQ97 | Leishmania braziliensis | 71% | 100% |
D0A414 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AU15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q0I0 | Leishmania major | 89% | 100% |