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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9ANI0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.649 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.608 |
DEG_SCF_FBW7_2 | 359 | 364 | PF00400 | 0.535 |
DEG_SIAH_1 | 474 | 482 | PF03145 | 0.638 |
DOC_CDC14_PxL_1 | 161 | 169 | PF14671 | 0.481 |
DOC_CKS1_1 | 134 | 139 | PF01111 | 0.724 |
DOC_CYCLIN_yClb1_LxF_4 | 430 | 435 | PF00134 | 0.550 |
DOC_PP1_RVXF_1 | 299 | 306 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 430 | 436 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.665 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.656 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.618 |
DOC_USP7_UBL2_3 | 390 | 394 | PF12436 | 0.601 |
DOC_USP7_UBL2_3 | 4 | 8 | PF12436 | 0.677 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 142 | 146 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 355 | 360 | PF00244 | 0.640 |
LIG_Actin_WH2_2 | 196 | 212 | PF00022 | 0.628 |
LIG_Actin_WH2_2 | 311 | 328 | PF00022 | 0.611 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.413 |
LIG_BIR_III_2 | 437 | 441 | PF00653 | 0.567 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.675 |
LIG_EVH1_2 | 440 | 444 | PF00568 | 0.492 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.687 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.649 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.527 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.680 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.666 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.716 |
LIG_GBD_Chelix_1 | 185 | 193 | PF00786 | 0.619 |
LIG_HP1_1 | 481 | 485 | PF01393 | 0.680 |
LIG_LIR_Apic_2 | 128 | 134 | PF02991 | 0.512 |
LIG_LIR_Apic_2 | 302 | 308 | PF02991 | 0.601 |
LIG_LIR_Gen_1 | 313 | 321 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.715 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.684 |
LIG_LYPXL_SIV_4 | 449 | 457 | PF13949 | 0.453 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.691 |
LIG_SH2_CRK | 446 | 450 | PF00017 | 0.613 |
LIG_SH2_NCK_1 | 131 | 135 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.605 |
LIG_SH3_1 | 131 | 137 | PF00018 | 0.686 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.783 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.652 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.640 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.609 |
LIG_SUMO_SIM_anti_2 | 480 | 486 | PF11976 | 0.607 |
LIG_SUMO_SIM_par_1 | 267 | 273 | PF11976 | 0.622 |
LIG_TRFH_1 | 262 | 266 | PF08558 | 0.632 |
LIG_TRFH_1 | 304 | 308 | PF08558 | 0.593 |
LIG_WW_3 | 328 | 332 | PF00397 | 0.638 |
MOD_CDK_SPK_2 | 401 | 406 | PF00069 | 0.750 |
MOD_CDK_SPxK_1 | 426 | 432 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.693 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.784 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.687 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.711 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.578 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.655 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.782 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.546 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.631 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.690 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.717 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.783 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.627 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.615 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.823 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.555 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.679 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.731 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.626 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.568 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.742 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.547 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.545 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.588 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.750 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.733 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.633 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.577 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.654 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.656 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.693 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.576 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.541 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.723 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.611 |
MOD_OFUCOSY | 163 | 170 | PF10250 | 0.621 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.609 |
MOD_PK_1 | 355 | 361 | PF00069 | 0.592 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.705 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.562 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.693 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.763 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.612 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.673 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.650 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.618 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.568 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.727 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.738 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.654 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.552 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.662 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.751 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.636 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.745 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.546 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.660 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.659 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.553 |
TRG_NLS_MonoCore_2 | 3 | 8 | PF00514 | 0.651 |
TRG_NLS_MonoExtC_3 | 3 | 8 | PF00514 | 0.611 |
TRG_NLS_MonoExtC_3 | 393 | 398 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 392 | 398 | PF00514 | 0.643 |
TRG_NLS_MonoExtN_4 | 4 | 10 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 340 | 345 | PF00026 | 0.654 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I8Z9 | Leishmania donovani | 78% | 100% |
A4H6F1 | Leishmania braziliensis | 65% | 96% |
A4HUU5 | Leishmania infantum | 76% | 100% |
Q4QH46 | Leishmania major | 78% | 99% |