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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q0J2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.456 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.658 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.542 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.501 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.606 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.671 |
DOC_CYCLIN_RxL_1 | 137 | 150 | PF00134 | 0.355 |
DOC_CYCLIN_yCln2_LP_2 | 246 | 249 | PF00134 | 0.435 |
DOC_MAPK_MEF2A_6 | 118 | 125 | PF00069 | 0.519 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.556 |
DOC_PP2B_LxvP_1 | 309 | 312 | PF13499 | 0.591 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.558 |
DOC_PP4_FxxP_1 | 295 | 298 | PF00568 | 0.591 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.619 |
DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.473 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.572 |
DOC_USP7_UBL2_3 | 54 | 58 | PF12436 | 0.492 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.682 |
LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.493 |
LIG_APCC_ABBA_1 | 161 | 166 | PF00400 | 0.523 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.483 |
LIG_LIR_Apic_2 | 284 | 289 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 150 | 157 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.553 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.539 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.620 |
LIG_SH2_SRC | 178 | 181 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.514 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.455 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.538 |
LIG_SUMO_SIM_par_1 | 121 | 128 | PF11976 | 0.474 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.637 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.589 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.494 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.419 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.637 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.469 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.602 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.589 |
MOD_LATS_1 | 50 | 56 | PF00433 | 0.580 |
MOD_LATS_1 | 83 | 89 | PF00433 | 0.504 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.394 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.630 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.515 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.426 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.558 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.451 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.389 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.523 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.466 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.613 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.680 |
MOD_SUMO_rev_2 | 236 | 244 | PF00179 | 0.701 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 264 | 268 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 43 | 47 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGJ4 | Leptomonas seymouri | 76% | 99% |
A0A0S4IS55 | Bodo saltans | 45% | 100% |
A0A1X0P0I2 | Trypanosomatidae | 59% | 100% |
A0A3R7M3K5 | Trypanosoma rangeli | 55% | 100% |
A0A3S7XBV5 | Leishmania donovani | 95% | 100% |
A4HQ85 | Leishmania braziliensis | 85% | 100% |
A4IDY3 | Leishmania infantum | 95% | 100% |
D0A426 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9AU03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |