| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3Q8IF96
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.701 |
| CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.526 |
| CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.732 |
| CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.539 |
| CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.632 |
| CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.618 |
| CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.596 |
| CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.732 |
| CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.529 |
| CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.542 |
| CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.630 |
| CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.552 |
| CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.649 |
| CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.735 |
| DEG_COP1_1 | 165 | 176 | PF00400 | 0.583 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.750 |
| DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.693 |
| DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.691 |
| DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.663 |
| DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.477 |
| DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.821 |
| DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.605 |
| DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.636 |
| DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.738 |
| DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.710 |
| LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.591 |
| LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.704 |
| LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.626 |
| LIG_14-3-3_CterR_2 | 223 | 226 | PF00244 | 0.679 |
| LIG_APCC_ABBA_1 | 118 | 123 | PF00400 | 0.710 |
| LIG_FHA_1 | 168 | 174 | PF00498 | 0.652 |
| LIG_FHA_1 | 38 | 44 | PF00498 | 0.570 |
| LIG_FHA_2 | 104 | 110 | PF00498 | 0.686 |
| LIG_FHA_2 | 55 | 61 | PF00498 | 0.644 |
| LIG_LIR_Gen_1 | 133 | 143 | PF02991 | 0.644 |
| LIG_LIR_Gen_1 | 192 | 203 | PF02991 | 0.582 |
| LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.660 |
| LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.579 |
| LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.531 |
| LIG_SH2_CRK | 135 | 139 | PF00017 | 0.651 |
| LIG_SH2_CRK | 68 | 72 | PF00017 | 0.702 |
| LIG_SH2_NCK_1 | 68 | 72 | PF00017 | 0.702 |
| LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.623 |
| LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.650 |
| LIG_SH3_3 | 111 | 117 | PF00018 | 0.639 |
| LIG_SH3_3 | 200 | 206 | PF00018 | 0.672 |
| LIG_SH3_3 | 22 | 28 | PF00018 | 0.696 |
| LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.599 |
| MOD_CK1_1 | 112 | 118 | PF00069 | 0.665 |
| MOD_CK1_1 | 127 | 133 | PF00069 | 0.700 |
| MOD_CK1_1 | 159 | 165 | PF00069 | 0.708 |
| MOD_CK1_1 | 172 | 178 | PF00069 | 0.609 |
| MOD_CK2_1 | 127 | 133 | PF00069 | 0.571 |
| MOD_CK2_1 | 159 | 165 | PF00069 | 0.789 |
| MOD_CK2_1 | 178 | 184 | PF00069 | 0.611 |
| MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.751 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.680 |
| MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.710 |
| MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.808 |
| MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.675 |
| MOD_GSK3_1 | 109 | 116 | PF00069 | 0.694 |
| MOD_GSK3_1 | 124 | 131 | PF00069 | 0.654 |
| MOD_GSK3_1 | 172 | 179 | PF00069 | 0.607 |
| MOD_GSK3_1 | 189 | 196 | PF00069 | 0.650 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.705 |
| MOD_GSK3_1 | 86 | 93 | PF00069 | 0.751 |
| MOD_LATS_1 | 92 | 98 | PF00433 | 0.677 |
| MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.694 |
| MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.747 |
| MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.627 |
| MOD_NEK2_1 | 157 | 162 | PF00069 | 0.578 |
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.752 |
| MOD_NEK2_1 | 29 | 34 | PF00069 | 0.737 |
| MOD_NEK2_1 | 43 | 48 | PF00069 | 0.556 |
| MOD_NEK2_1 | 54 | 59 | PF00069 | 0.595 |
| MOD_PIKK_1 | 43 | 49 | PF00454 | 0.567 |
| MOD_PK_1 | 169 | 175 | PF00069 | 0.728 |
| MOD_PKA_1 | 149 | 155 | PF00069 | 0.598 |
| MOD_PKA_2 | 131 | 137 | PF00069 | 0.696 |
| MOD_PKA_2 | 176 | 182 | PF00069 | 0.537 |
| MOD_PKA_2 | 3 | 9 | PF00069 | 0.705 |
| MOD_PKA_2 | 66 | 72 | PF00069 | 0.633 |
| MOD_Plk_1 | 29 | 35 | PF00069 | 0.594 |
| MOD_Plk_4 | 20 | 26 | PF00069 | 0.611 |
| MOD_Plk_4 | 71 | 77 | PF00069 | 0.798 |
| MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.634 |
| MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.741 |
| MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.709 |
| TRG_DiLeu_BaEn_1 | 210 | 215 | PF01217 | 0.664 |
| TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.635 |
| TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.717 |
| TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.607 |
| TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.594 |
| TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.762 |
| TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.625 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I154 | Leptomonas seymouri | 41% | 99% |
| A4HH80 | Leishmania braziliensis | 62% | 100% |
| A4I4C6 | Leishmania infantum | 98% | 100% |
| E9ADS5 | Leishmania major | 86% | 100% |
| E9AM05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |