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: E9AE80
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.768 |
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.727 |
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.824 |
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.749 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.825 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.728 |
CLV_PCSK_FUR_1 | 197 | 201 | PF00082 | 0.814 |
CLV_PCSK_FUR_1 | 442 | 446 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.825 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.782 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 86 | 88 | PF00082 | 0.730 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.736 |
CLV_PCSK_PC7_1 | 196 | 202 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.714 |
DEG_APCC_DBOX_1 | 319 | 327 | PF00400 | 0.411 |
DEG_APCC_DBOX_1 | 446 | 454 | PF00400 | 0.436 |
DOC_CYCLIN_RxL_1 | 241 | 252 | PF00134 | 0.634 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.424 |
DOC_MAPK_JIP1_4 | 320 | 326 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 418 | 424 | PF00149 | 0.411 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.817 |
DOC_PP4_FxxP_1 | 335 | 338 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.842 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 381 | 388 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 47 | 63 | PF00022 | 0.583 |
LIG_BIR_III_4 | 216 | 220 | PF00653 | 0.594 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.836 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 62 | 66 | PF00533 | 0.686 |
LIG_deltaCOP1_diTrp_1 | 288 | 296 | PF00928 | 0.436 |
LIG_EH_1 | 332 | 336 | PF12763 | 0.411 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.700 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.606 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.593 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.642 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.732 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.706 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.763 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.741 |
LIG_LIR_Apic_2 | 137 | 143 | PF02991 | 0.823 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.372 |
LIG_MYND_1 | 334 | 338 | PF01753 | 0.411 |
LIG_REV1ctd_RIR_1 | 64 | 73 | PF16727 | 0.652 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.513 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.389 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.839 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.692 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.761 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.406 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.438 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.762 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.705 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.741 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.777 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.762 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.731 |
MOD_Cter_Amidation | 84 | 87 | PF01082 | 0.763 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.714 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.733 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.699 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.411 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.411 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.606 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.776 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.752 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.833 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.796 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.735 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.444 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.443 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.744 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.602 |
MOD_LATS_1 | 455 | 461 | PF00433 | 0.708 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.662 |
MOD_N-GLC_2 | 303 | 305 | PF02516 | 0.375 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.605 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.692 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.513 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.579 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.753 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.826 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.685 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.782 |
MOD_PKA_1 | 101 | 107 | PF00069 | 0.724 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.679 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.813 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.739 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.737 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.540 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.453 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.419 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.736 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.698 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.671 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.411 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.802 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.411 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.574 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.513 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.717 |
MOD_SUMO_for_1 | 336 | 339 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 19 | 28 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 339 | 348 | PF00179 | 0.395 |
MOD_SUMO_rev_2 | 410 | 419 | PF00179 | 0.389 |
TRG_DiLeu_BaEn_4 | 391 | 397 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.610 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 196 | 199 | PF00400 | 0.774 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.506 |
TRG_NLS_Bipartite_1 | 86 | 104 | PF00514 | 0.801 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKX8 | Leptomonas seymouri | 52% | 98% |
A0A3Q8IEK2 | Leishmania donovani | 89% | 100% |
A4HHL8 | Leishmania braziliensis | 73% | 95% |
A4I4S7 | Leishmania infantum | 89% | 100% |
E9ALK5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |