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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALN3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.593 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.745 |
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.694 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 374 | 378 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.732 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.500 |
CLV_PCSK_PC7_1 | 374 | 380 | PF00082 | 0.429 |
CLV_PCSK_PC7_1 | 66 | 72 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.462 |
CLV_Separin_Metazoa | 371 | 375 | PF03568 | 0.487 |
DOC_CYCLIN_RxL_1 | 10 | 24 | PF00134 | 0.326 |
DOC_CYCLIN_yCln2_LP_2 | 178 | 184 | PF00134 | 0.357 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 95 | 101 | PF00069 | 0.791 |
DOC_PP1_RVXF_1 | 14 | 21 | PF00149 | 0.316 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.385 |
DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.525 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.478 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 400 | 404 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.495 |
LIG_14-3-3_CanoR_1 | 100 | 110 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 324 | 332 | PF00244 | 0.799 |
LIG_14-3-3_CanoR_1 | 377 | 385 | PF00244 | 0.457 |
LIG_Actin_WH2_2 | 159 | 177 | PF00022 | 0.439 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.534 |
LIG_deltaCOP1_diTrp_1 | 282 | 288 | PF00928 | 0.430 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.404 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.646 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.472 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.396 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.365 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.424 |
LIG_LIR_Apic_2 | 255 | 261 | PF02991 | 0.497 |
LIG_LIR_Apic_2 | 38 | 44 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 282 | 288 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.443 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.435 |
LIG_SH2_NCK_1 | 394 | 398 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.413 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.726 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.554 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.346 |
LIG_SUMO_SIM_par_1 | 443 | 449 | PF11976 | 0.400 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.612 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.460 |
LIG_WRC_WIRS_1 | 285 | 290 | PF05994 | 0.436 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.709 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.680 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.584 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.438 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.750 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.719 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.607 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.417 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.367 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.427 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.523 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.545 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.527 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.759 |
MOD_GlcNHglycan | 299 | 305 | PF01048 | 0.737 |
MOD_GlcNHglycan | 312 | 316 | PF01048 | 0.735 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.584 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.558 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.518 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.710 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.675 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.679 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.529 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.515 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.529 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.657 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.603 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.624 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.473 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.513 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.667 |
MOD_NEK2_2 | 443 | 448 | PF00069 | 0.405 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.806 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.406 |
MOD_PKA_1 | 322 | 328 | PF00069 | 0.774 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.441 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.605 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.406 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.789 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.484 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.539 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.484 |
MOD_PKB_1 | 322 | 330 | PF00069 | 0.682 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.729 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.622 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.600 |
MOD_Plk_2-3 | 119 | 125 | PF00069 | 0.480 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.501 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.464 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.393 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.487 |
MOD_SUMO_rev_2 | 212 | 217 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 318 | 325 | PF00179 | 0.748 |
TRG_DiLeu_BaEn_1 | 398 | 403 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.390 |
TRG_DiLeu_BaEn_2 | 413 | 419 | PF01217 | 0.595 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.531 |
TRG_ER_FFAT_1 | 413 | 424 | PF00635 | 0.378 |
TRG_NLS_MonoExtC_3 | 322 | 328 | PF00514 | 0.706 |
TRG_NLS_MonoExtC_3 | 376 | 382 | PF00514 | 0.413 |
TRG_NLS_MonoExtN_4 | 322 | 327 | PF00514 | 0.787 |
TRG_NLS_MonoExtN_4 | 374 | 381 | PF00514 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 359 | 363 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 70 | 75 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB34 | Leptomonas seymouri | 49% | 87% |
A0A0S4JH57 | Bodo saltans | 27% | 85% |
A0A1X0P158 | Trypanosomatidae | 32% | 100% |
A0A3R7MJJ2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7X2K3 | Leishmania donovani | 91% | 98% |
A4HHJ1 | Leishmania braziliensis | 75% | 100% |
A4I4P9 | Leishmania infantum | 91% | 98% |
C9ZLD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AE52 | Leishmania major | 88% | 100% |
V5BGH3 | Trypanosoma cruzi | 30% | 100% |