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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q8E8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.588 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.717 |
DOC_CYCLIN_RxL_1 | 64 | 73 | PF00134 | 0.603 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.595 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.521 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 107 | 113 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 40 | 49 | PF00244 | 0.569 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BIR_III_2 | 204 | 208 | PF00653 | 0.594 |
LIG_BRCT_MDC1_1 | 222 | 226 | PF00533 | 0.556 |
LIG_eIF4E_1 | 64 | 70 | PF01652 | 0.579 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.571 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.645 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.603 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.621 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.499 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.694 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.613 |
LIG_LIR_Apic_2 | 168 | 173 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.734 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.527 |
LIG_REV1ctd_RIR_1 | 34 | 44 | PF16727 | 0.718 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.656 |
LIG_SH2_GRB2like | 9 | 12 | PF00017 | 0.601 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.538 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.668 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.635 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.710 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.681 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.734 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.580 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.513 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.591 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.661 |
MOD_GlcNHglycan | 12 | 16 | PF01048 | 0.697 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.661 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.666 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.582 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.689 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.667 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.630 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.549 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.543 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.596 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.492 |
MOD_N-GLC_1 | 51 | 56 | PF02516 | 0.623 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.627 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.604 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.530 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.653 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.649 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.647 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.535 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.572 |
MOD_NEK2_2 | 32 | 37 | PF00069 | 0.622 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.600 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.581 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.658 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.524 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.593 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.580 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.563 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.637 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.493 |
MOD_Plk_2-3 | 131 | 137 | PF00069 | 0.578 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.518 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.548 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.531 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.670 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.724 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.660 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.608 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.730 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.596 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.623 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYM4 | Trypanosomatidae | 43% | 94% |
A0A3Q8IDW1 | Leishmania donovani | 95% | 100% |
A0A422N2Z7 | Trypanosoma rangeli | 37% | 89% |
A4HGG5 | Leishmania braziliensis | 83% | 100% |
A4I3J7 | Leishmania infantum | 95% | 100% |
D0A7U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 91% |
E9AZT7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |