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: Q4Q1A5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.620 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.594 |
DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.649 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 126 | 136 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 181 | 188 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 60 | 68 | PF00244 | 0.663 |
LIG_Actin_WH2_2 | 6 | 24 | PF00022 | 0.612 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.662 |
LIG_BIR_III_2 | 162 | 166 | PF00653 | 0.659 |
LIG_BRCT_BRCA1_1 | 163 | 167 | PF00533 | 0.644 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.695 |
LIG_deltaCOP1_diTrp_1 | 201 | 205 | PF00928 | 0.507 |
LIG_deltaCOP1_diTrp_1 | 211 | 217 | PF00928 | 0.523 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.615 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.650 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.547 |
LIG_IRF3_LxIS_1 | 228 | 235 | PF10401 | 0.450 |
LIG_LIR_Gen_1 | 211 | 219 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.515 |
LIG_PDZ_Class_3 | 244 | 249 | PF00595 | 0.596 |
LIG_SH2_PTP2 | 67 | 70 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.491 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.652 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.551 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.633 |
LIG_SUMO_SIM_anti_2 | 66 | 72 | PF11976 | 0.569 |
LIG_SUMO_SIM_par_1 | 145 | 153 | PF11976 | 0.651 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.516 |
MOD_CDK_SPxxK_3 | 37 | 44 | PF00069 | 0.641 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.591 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.554 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.616 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.712 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.628 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.552 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.505 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.623 |
MOD_CMANNOS | 202 | 205 | PF00535 | 0.489 |
MOD_DYRK1A_RPxSP_1 | 37 | 41 | PF00069 | 0.516 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.608 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.602 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.473 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.727 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.624 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.727 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.703 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.623 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.597 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.572 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.636 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.603 |
MOD_NEK2_2 | 121 | 126 | PF00069 | 0.435 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.644 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.748 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.663 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.637 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.600 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.697 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.645 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.482 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.573 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.637 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.617 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.608 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.705 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.721 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.611 |
TRG_DiLeu_BaEn_4 | 238 | 244 | PF01217 | 0.506 |
TRG_DiLeu_BaLyEn_6 | 108 | 113 | PF01217 | 0.597 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.661 |
TRG_DiLeu_BaLyEn_6 | 223 | 228 | PF01217 | 0.565 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.491 |
TRG_NLS_MonoExtN_4 | 105 | 112 | PF00514 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.600 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1D7 | Leptomonas seymouri | 51% | 100% |
A0A1X0P4K6 | Trypanosomatidae | 29% | 100% |
A0A3Q8IW55 | Leishmania donovani | 92% | 100% |
A0A3R7NG27 | Trypanosoma rangeli | 32% | 100% |
A4HPI0 | Leishmania braziliensis | 82% | 100% |
A4IDA2 | Leishmania infantum | 92% | 100% |
D0A8E2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AT92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DA52 | Trypanosoma cruzi | 33% | 100% |