| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q9GN98
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.478 |
| CLV_C14_Caspase3-7 | 199 | 203 | PF00656 | 0.428 |
| CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.626 |
| CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.486 |
| CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.590 |
| CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.439 |
| CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.672 |
| CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.490 |
| CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.377 |
| CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.637 |
| CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.650 |
| CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.520 |
| CLV_PCSK_PC7_1 | 209 | 215 | PF00082 | 0.497 |
| CLV_PCSK_PC7_1 | 243 | 249 | PF00082 | 0.634 |
| CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.533 |
| DEG_SCF_TRCP1_1 | 232 | 238 | PF00400 | 0.584 |
| DOC_CYCLIN_RxL_1 | 156 | 167 | PF00134 | 0.543 |
| DOC_PP2B_PxIxI_1 | 12 | 18 | PF00149 | 0.430 |
| DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.694 |
| DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.751 |
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.693 |
| DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.564 |
| DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.716 |
| DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.608 |
| LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.742 |
| LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.487 |
| LIG_14-3-3_CanoR_1 | 37 | 41 | PF00244 | 0.452 |
| LIG_14-3-3_CterR_2 | 246 | 249 | PF00244 | 0.604 |
| LIG_Actin_WH2_2 | 185 | 203 | PF00022 | 0.538 |
| LIG_FHA_1 | 12 | 18 | PF00498 | 0.383 |
| LIG_FHA_1 | 158 | 164 | PF00498 | 0.528 |
| LIG_FHA_1 | 37 | 43 | PF00498 | 0.431 |
| LIG_FHA_2 | 110 | 116 | PF00498 | 0.575 |
| LIG_LIR_Apic_2 | 107 | 111 | PF02991 | 0.510 |
| LIG_MYND_1 | 83 | 87 | PF01753 | 0.553 |
| LIG_Pex14_2 | 104 | 108 | PF04695 | 0.417 |
| LIG_PTB_Apo_2 | 27 | 34 | PF02174 | 0.468 |
| LIG_REV1ctd_RIR_1 | 31 | 41 | PF16727 | 0.484 |
| LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.335 |
| LIG_SH3_1 | 84 | 90 | PF00018 | 0.541 |
| LIG_SH3_3 | 80 | 86 | PF00018 | 0.524 |
| LIG_SxIP_EBH_1 | 234 | 248 | PF03271 | 0.447 |
| LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.587 |
| MOD_CDK_SPK_2 | 79 | 84 | PF00069 | 0.627 |
| MOD_CK1_1 | 123 | 129 | PF00069 | 0.617 |
| MOD_CK1_1 | 54 | 60 | PF00069 | 0.704 |
| MOD_CK1_1 | 6 | 12 | PF00069 | 0.420 |
| MOD_CK1_1 | 79 | 85 | PF00069 | 0.426 |
| MOD_CK2_1 | 109 | 115 | PF00069 | 0.520 |
| MOD_CK2_1 | 21 | 27 | PF00069 | 0.406 |
| MOD_CK2_1 | 62 | 68 | PF00069 | 0.694 |
| MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.720 |
| MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.513 |
| MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.518 |
| MOD_GlcNHglycan | 218 | 223 | PF01048 | 0.541 |
| MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.722 |
| MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.599 |
| MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.667 |
| MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.693 |
| MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.747 |
| MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.635 |
| MOD_GSK3_1 | 120 | 127 | PF00069 | 0.636 |
| MOD_GSK3_1 | 218 | 225 | PF00069 | 0.598 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.636 |
| MOD_GSK3_1 | 63 | 70 | PF00069 | 0.744 |
| MOD_NEK2_1 | 96 | 101 | PF00069 | 0.377 |
| MOD_PIKK_1 | 141 | 147 | PF00454 | 0.736 |
| MOD_PKA_2 | 146 | 152 | PF00069 | 0.481 |
| MOD_PKA_2 | 230 | 236 | PF00069 | 0.595 |
| MOD_PKA_2 | 36 | 42 | PF00069 | 0.429 |
| MOD_PKA_2 | 96 | 102 | PF00069 | 0.534 |
| MOD_Plk_1 | 157 | 163 | PF00069 | 0.499 |
| MOD_Plk_4 | 11 | 17 | PF00069 | 0.390 |
| MOD_Plk_4 | 187 | 193 | PF00069 | 0.608 |
| MOD_Plk_4 | 236 | 242 | PF00069 | 0.476 |
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.690 |
| MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.569 |
| MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.717 |
| TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.344 |
| TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.587 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5V4 | Leptomonas seymouri | 51% | 100% |
| A0A1X0NIU6 | Trypanosomatidae | 32% | 100% |
| A0A3R7JUY0 | Trypanosoma rangeli | 30% | 100% |
| A0A3S7X907 | Leishmania donovani | 93% | 100% |
| A4HMF1 | Leishmania braziliensis | 72% | 100% |
| A4IB23 | Leishmania infantum | 92% | 100% |
| C9ZNL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| E9B608 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |