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 |
Related structures:
AlphaFold database: E9B5Q4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.264 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.616 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.538 |
DOC_CYCLIN_RxL_1 | 208 | 218 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.486 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.455 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.502 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.279 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.419 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.400 |
LIG_APCC_ABBA_1 | 119 | 124 | PF00400 | 0.167 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.375 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.609 |
LIG_Clathr_ClatBox_1 | 240 | 244 | PF01394 | 0.533 |
LIG_deltaCOP1_diTrp_1 | 244 | 249 | PF00928 | 0.655 |
LIG_EH_1 | 201 | 205 | PF12763 | 0.436 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.409 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.504 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.321 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.442 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.301 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.552 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.585 |
LIG_LIR_Apic_2 | 112 | 118 | PF02991 | 0.283 |
LIG_LIR_Apic_2 | 43 | 48 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 129 | 137 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 244 | 254 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 272 | 278 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.689 |
LIG_PCNA_yPIPBox_3 | 20 | 28 | PF02747 | 0.565 |
LIG_Pex14_2 | 115 | 119 | PF04695 | 0.264 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.557 |
LIG_REV1ctd_RIR_1 | 66 | 74 | PF16727 | 0.450 |
LIG_REV1ctd_RIR_1 | 94 | 103 | PF16727 | 0.264 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.559 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.614 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.584 |
LIG_SUMO_SIM_par_1 | 142 | 147 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 239 | 244 | PF11976 | 0.533 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.673 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.279 |
LIG_UBA3_1 | 3 | 9 | PF00899 | 0.382 |
MOD_CDK_SPxK_1 | 38 | 44 | PF00069 | 0.458 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.636 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.635 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.642 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.646 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.547 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.650 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.518 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.605 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.432 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.557 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.681 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.440 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.453 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.684 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.706 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.392 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.406 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.584 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.405 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.579 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.580 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.434 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.503 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.555 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.279 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.617 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.542 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P611 | Leptomonas seymouri | 64% | 85% |
A0A0S4JHS2 | Bodo saltans | 34% | 71% |
A0A1X0NJ57 | Trypanosomatidae | 45% | 90% |
A0A3R7LQI0 | Trypanosoma rangeli | 47% | 89% |
A0A3S7X8M8 | Leishmania donovani | 93% | 88% |
A4HM55 | Leishmania braziliensis | 86% | 100% |
A4IAR7 | Leishmania infantum | 93% | 88% |
D0A2E5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 90% |
E9AEJ3 | Leishmania major | 93% | 100% |
V5DJR0 | Trypanosoma cruzi | 48% | 89% |