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: E9AE69
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 312 | 316 | PF00656 | 0.660 |
CLV_MEL_PAP_1 | 256 | 262 | PF00089 | 0.503 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.551 |
CLV_PCSK_FUR_1 | 217 | 221 | PF00082 | 0.698 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.630 |
CLV_PCSK_FUR_1 | 296 | 300 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.637 |
CLV_PCSK_PC7_1 | 292 | 298 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.676 |
DEG_SPOP_SBC_1 | 369 | 373 | PF00917 | 0.657 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.685 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.573 |
DOC_CYCLIN_yCln2_LP_2 | 3 | 9 | PF00134 | 0.514 |
DOC_MAPK_DCC_7 | 37 | 46 | PF00069 | 0.738 |
DOC_MAPK_gen_1 | 243 | 253 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 190 | 199 | PF00069 | 0.624 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.738 |
DOC_PP4_FxxP_1 | 435 | 438 | PF00568 | 0.692 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.660 |
DOC_USP7_UBL2_3 | 279 | 283 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 378 | 382 | PF12436 | 0.720 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 159 | 163 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 390 | 398 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 425 | 430 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 43 | 52 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.707 |
LIG_BIR_III_4 | 327 | 331 | PF00653 | 0.697 |
LIG_FAT_LD_1 | 128 | 136 | PF03623 | 0.549 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.508 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.610 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.568 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.741 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.734 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.558 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.632 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.729 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.677 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.727 |
LIG_Integrin_isoDGR_2 | 364 | 366 | PF01839 | 0.602 |
LIG_IRF3_LxIS_1 | 197 | 204 | PF10401 | 0.613 |
LIG_LIR_Apic_2 | 351 | 356 | PF02991 | 0.796 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.724 |
LIG_MAD2 | 16 | 24 | PF02301 | 0.687 |
LIG_NRBOX | 90 | 96 | PF00104 | 0.636 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.637 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.621 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.590 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.797 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.700 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.669 |
LIG_SH3_4 | 378 | 385 | PF00018 | 0.720 |
LIG_SUMO_SIM_anti_2 | 168 | 173 | PF11976 | 0.628 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.737 |
LIG_SUMO_SIM_par_1 | 249 | 255 | PF11976 | 0.481 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.746 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.730 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.636 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.643 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.779 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.693 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.734 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.733 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.734 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.708 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.719 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.750 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.800 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.743 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.708 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.713 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.617 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.651 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.710 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.796 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.663 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.792 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.530 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.521 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.638 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.702 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.695 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.700 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.596 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.531 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.628 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.514 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.608 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.621 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.728 |
MOD_NEK2_2 | 381 | 386 | PF00069 | 0.646 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.594 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.799 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.618 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.720 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.426 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.718 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.670 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.516 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.726 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.523 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.790 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.839 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.751 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.766 |
MOD_PKB_1 | 299 | 307 | PF00069 | 0.624 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.762 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.636 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.517 |
MOD_Plk_2-3 | 111 | 117 | PF00069 | 0.762 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.761 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.695 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.758 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.809 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.747 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.686 |
TRG_DiLeu_BaLyEn_6 | 86 | 91 | PF01217 | 0.656 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.726 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.802 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.686 |
TRG_NES_CRM1_1 | 134 | 147 | PF08389 | 0.456 |
TRG_NLS_MonoCore_2 | 376 | 381 | PF00514 | 0.718 |
TRG_NLS_MonoExtC_3 | 278 | 283 | PF00514 | 0.692 |
TRG_NLS_MonoExtN_4 | 279 | 284 | PF00514 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 285 | 289 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW7 | Leptomonas seymouri | 29% | 100% |
A0A3Q8IRH8 | Leishmania donovani | 84% | 99% |
A4HHK6 | Leishmania braziliensis | 53% | 100% |
A4I4R7 | Leishmania infantum | 84% | 99% |
E9ALL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |