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: A4HM55
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.269 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.287 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.662 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.454 |
DOC_CYCLIN_RxL_1 | 185 | 195 | PF00134 | 0.552 |
DOC_PP2B_LxvP_1 | 231 | 234 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 24 | 27 | PF13499 | 0.577 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.287 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.287 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 240 | 244 | PF00244 | 0.626 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.644 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.402 |
LIG_Clathr_ClatBox_1 | 217 | 221 | PF01394 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 221 | 226 | PF00928 | 0.624 |
LIG_EH_1 | 178 | 182 | PF12763 | 0.507 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.496 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.647 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.554 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.570 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.652 |
LIG_LIR_Apic_2 | 20 | 25 | PF02991 | 0.603 |
LIG_LIR_Apic_2 | 89 | 95 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 213 | 220 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.656 |
LIG_Pex14_2 | 4 | 8 | PF04695 | 0.671 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.269 |
LIG_REV1ctd_RIR_1 | 43 | 51 | PF16727 | 0.585 |
LIG_REV1ctd_RIR_1 | 71 | 80 | PF16727 | 0.269 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.654 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.627 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.638 |
LIG_SUMO_SIM_par_1 | 117 | 124 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 216 | 221 | PF11976 | 0.500 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.698 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.269 |
MOD_CDK_SPxK_1 | 15 | 21 | PF00069 | 0.551 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.434 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.445 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.559 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.675 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.698 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.419 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.670 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.680 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.553 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.533 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.540 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.515 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.649 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.561 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.530 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.662 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.424 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.555 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.712 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.504 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.617 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.582 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.415 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.558 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.539 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.603 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.655 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.518 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.576 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.566 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.287 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P611 | Leptomonas seymouri | 64% | 78% |
A0A1X0NJ57 | Trypanosomatidae | 47% | 82% |
A0A3R7LQI0 | Trypanosoma rangeli | 47% | 82% |
A0A3S7X8M8 | Leishmania donovani | 86% | 81% |
A4IAR7 | Leishmania infantum | 86% | 81% |
D0A2E5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 83% |
E9AEJ3 | Leishmania major | 85% | 100% |
E9B5Q4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 92% |
V5DJR0 | Trypanosoma cruzi | 49% | 82% |