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: E9AEJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.264 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.554 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.502 |
DOC_CYCLIN_RxL_1 | 208 | 218 | PF00134 | 0.420 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.515 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.279 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.380 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.364 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.279 |
LIG_14-3-3_CanoR_1 | 236 | 241 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 263 | 267 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 44 | 48 | PF00244 | 0.367 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.371 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.644 |
LIG_Clathr_ClatBox_1 | 240 | 244 | PF01394 | 0.528 |
LIG_deltaCOP1_diTrp_1 | 244 | 249 | PF00928 | 0.646 |
LIG_EH_1 | 201 | 205 | PF12763 | 0.412 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.424 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.496 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.401 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.546 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.573 |
LIG_LIR_Apic_2 | 112 | 118 | PF02991 | 0.283 |
LIG_LIR_Apic_2 | 43 | 48 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 129 | 137 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 244 | 254 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.689 |
LIG_PCNA_yPIPBox_3 | 20 | 28 | PF02747 | 0.567 |
LIG_Pex14_2 | 115 | 119 | PF04695 | 0.264 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.544 |
LIG_REV1ctd_RIR_1 | 66 | 74 | PF16727 | 0.427 |
LIG_REV1ctd_RIR_1 | 94 | 103 | PF16727 | 0.264 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.601 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.656 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.577 |
LIG_SUMO_SIM_par_1 | 142 | 147 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 239 | 244 | PF11976 | 0.526 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.665 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.279 |
LIG_UBA3_1 | 3 | 9 | PF00899 | 0.374 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.419 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.629 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.626 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.595 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.655 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.486 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.684 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.549 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.621 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.425 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.559 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.680 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.440 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.463 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.475 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.674 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.705 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.389 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.427 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.652 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.410 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.568 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.482 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.369 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.580 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.579 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.377 |
MOD_Plk_2-3 | 155 | 161 | PF00069 | 0.440 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.512 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.554 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.279 |
MOD_SUMO_rev_2 | 77 | 85 | PF00179 | 0.439 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P611 | Leptomonas seymouri | 62% | 85% |
A0A0S4JHS2 | Bodo saltans | 33% | 71% |
A0A1X0NJ57 | Trypanosomatidae | 43% | 90% |
A0A3R7LQI0 | Trypanosoma rangeli | 47% | 89% |
A0A3S7X8M8 | Leishmania donovani | 93% | 88% |
A4HM55 | Leishmania braziliensis | 85% | 100% |
A4IAR7 | Leishmania infantum | 93% | 88% |
D0A2E5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 90% |
E9B5Q4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5DJR0 | Trypanosoma cruzi | 49% | 89% |