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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IAH5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.736 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.748 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.414 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.335 |
DEG_APCC_DBOX_1 | 25 | 33 | PF00400 | 0.516 |
DEG_APCC_DBOX_1 | 288 | 296 | PF00400 | 0.395 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.662 |
DEG_SCF_FBW7_2 | 332 | 337 | PF00400 | 0.520 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.408 |
DOC_MAPK_DCC_7 | 286 | 296 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 160 | 166 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 286 | 296 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 319 | 329 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.457 |
DOC_MAPK_NFAT4_5 | 289 | 297 | PF00069 | 0.498 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.463 |
DOC_PP2B_LxvP_1 | 164 | 167 | PF13499 | 0.467 |
DOC_PP4_FxxP_1 | 82 | 85 | PF00568 | 0.536 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.721 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 141 | 151 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 324 | 328 | PF00244 | 0.500 |
LIG_Actin_WH2_2 | 114 | 130 | PF00022 | 0.517 |
LIG_BRCT_BRCA1_1 | 325 | 329 | PF00533 | 0.422 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.416 |
LIG_CaM_NSCaTE_8 | 28 | 35 | PF13499 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 73 | 82 | PF00928 | 0.508 |
LIG_EVH1_1 | 164 | 168 | PF00568 | 0.515 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.521 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.453 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.547 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.550 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.499 |
LIG_LIR_Apic_2 | 79 | 85 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.434 |
LIG_LIR_LC3C_4 | 185 | 189 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.470 |
LIG_MLH1_MIPbox_1 | 78 | 82 | PF16413 | 0.416 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.496 |
LIG_PCNA_yPIPBox_3 | 141 | 155 | PF02747 | 0.369 |
LIG_SH2_PTP2 | 267 | 270 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.440 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.452 |
LIG_SUMO_SIM_anti_2 | 123 | 128 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 144 | 153 | PF11976 | 0.522 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 292 | 297 | PF11976 | 0.493 |
LIG_WRC_WIRS_1 | 6 | 11 | PF05994 | 0.589 |
MOD_CDK_SPK_2 | 254 | 259 | PF00069 | 0.511 |
MOD_CDK_SPK_2 | 55 | 60 | PF00069 | 0.751 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.424 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.724 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.301 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.429 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.507 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.522 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.496 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.599 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.458 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.672 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.552 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.540 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.484 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.596 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.419 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.657 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.664 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.478 |
MOD_N-GLC_2 | 138 | 140 | PF02516 | 0.388 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.617 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.502 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.464 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.538 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.468 |
MOD_PKA_1 | 41 | 47 | PF00069 | 0.679 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.488 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.516 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.732 |
MOD_PKB_1 | 141 | 149 | PF00069 | 0.487 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.620 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.651 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.640 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.426 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.508 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.424 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.750 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.464 |
MOD_SUMO_for_1 | 117 | 120 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 147 | 152 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_1 | 229 | 234 | PF01217 | 0.398 |
TRG_DiLeu_BaEn_1 | 287 | 292 | PF01217 | 0.379 |
TRG_DiLeu_BaLyEn_6 | 290 | 295 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 63 | 66 | PF00400 | 0.702 |
TRG_NES_CRM1_1 | 107 | 123 | PF08389 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P703 | Leptomonas seymouri | 60% | 80% |
A0A0S4KKR7 | Bodo saltans | 32% | 66% |
A0A1X0PA52 | Trypanosomatidae | 46% | 84% |
A0A3S7X8N4 | Leishmania donovani | 100% | 100% |
A0A422NVD0 | Trypanosoma rangeli | 44% | 90% |
A4HBC7 | Leishmania braziliensis | 82% | 100% |
C9ZLR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 89% |
E9B5J9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q2D7 | Leishmania major | 91% | 100% |
V5BW32 | Trypanosoma cruzi | 41% | 89% |