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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AQS7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.683 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 418 | 420 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.721 |
CLV_Separin_Metazoa | 21 | 25 | PF03568 | 0.605 |
DEG_APCC_DBOX_1 | 235 | 243 | PF00400 | 0.646 |
DEG_APCC_DBOX_1 | 400 | 408 | PF00400 | 0.496 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.718 |
DOC_CKS1_1 | 213 | 218 | PF01111 | 0.580 |
DOC_CYCLIN_RxL_1 | 233 | 243 | PF00134 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.583 |
DOC_MAPK_DCC_7 | 205 | 213 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 418 | 426 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 205 | 213 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 397 | 404 | PF00069 | 0.613 |
DOC_MAPK_NFAT4_5 | 397 | 405 | PF00069 | 0.617 |
DOC_MAPK_RevD_3 | 405 | 419 | PF00069 | 0.452 |
DOC_MAPK_RevD_3 | 470 | 485 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.745 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.733 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.606 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.773 |
LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 332 | 339 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 352 | 357 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.493 |
LIG_APCC_ABBA_1 | 23 | 28 | PF00400 | 0.626 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.673 |
LIG_eIF4E_1 | 111 | 117 | PF01652 | 0.535 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.703 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.719 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.626 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.521 |
LIG_IRF3_LxIS_1 | 188 | 195 | PF10401 | 0.481 |
LIG_LIR_Apic_2 | 90 | 96 | PF02991 | 0.743 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 340 | 351 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.532 |
LIG_NRBOX | 112 | 118 | PF00104 | 0.535 |
LIG_PCNA_yPIPBox_3 | 19 | 27 | PF02747 | 0.609 |
LIG_PTAP_UEV_1 | 6 | 11 | PF05743 | 0.569 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.640 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.724 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.725 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.595 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.716 |
LIG_SUMO_SIM_anti_2 | 248 | 253 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 422 | 432 | PF11976 | 0.451 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.703 |
LIG_UBA3_1 | 250 | 259 | PF00899 | 0.630 |
LIG_WW_2 | 378 | 381 | PF00397 | 0.480 |
MOD_CDK_SPK_2 | 200 | 205 | PF00069 | 0.524 |
MOD_CDK_SPK_2 | 362 | 367 | PF00069 | 0.644 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.556 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.661 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.540 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.620 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.760 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.611 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.520 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.784 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.587 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.662 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.510 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.687 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.734 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.766 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.651 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.574 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.555 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.676 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.646 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.553 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.739 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.627 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.659 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.569 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.698 |
MOD_N-GLC_2 | 170 | 172 | PF02516 | 0.609 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.474 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.681 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.515 |
MOD_PIKK_1 | 145 | 151 | PF00454 | 0.605 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.627 |
MOD_PK_1 | 299 | 305 | PF00069 | 0.517 |
MOD_PK_1 | 439 | 445 | PF00069 | 0.490 |
MOD_PKA_1 | 372 | 378 | PF00069 | 0.699 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.605 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.768 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.718 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.699 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.621 |
MOD_PKB_1 | 437 | 445 | PF00069 | 0.670 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.508 |
MOD_Plk_2-3 | 134 | 140 | PF00069 | 0.783 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.701 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.447 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.640 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.662 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.691 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.728 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.572 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.696 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.687 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.579 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.772 |
TRG_DiLeu_BaEn_1 | 38 | 43 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.643 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.703 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.695 |
TRG_NLS_Bipartite_1 | 418 | 440 | PF00514 | 0.528 |
TRG_NLS_MonoCore_2 | 435 | 440 | PF00514 | 0.744 |
TRG_NLS_MonoExtC_3 | 435 | 441 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 433 | 440 | PF00514 | 0.739 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q0 | Leptomonas seymouri | 32% | 100% |
A0A3Q8IAM2 | Leishmania donovani | 88% | 100% |
A4H8P3 | Leishmania braziliensis | 74% | 100% |
A4HX13 | Leishmania infantum | 88% | 100% |
Q4QEQ1 | Leishmania major | 86% | 100% |