| 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: A4H815
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.717 |
| CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.717 |
| CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.583 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.630 |
| DEG_SCF_FBW7_1 | 244 | 249 | PF00400 | 0.555 |
| DEG_SPOP_SBC_1 | 236 | 240 | PF00917 | 0.584 |
| DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.671 |
| DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.699 |
| DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.604 |
| DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.677 |
| DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.626 |
| DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.695 |
| DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.656 |
| DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.599 |
| DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.699 |
| DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.547 |
| LIG_14-3-3_CanoR_1 | 130 | 138 | PF00244 | 0.733 |
| LIG_14-3-3_CanoR_1 | 256 | 262 | PF00244 | 0.549 |
| LIG_eIF4E_1 | 4 | 10 | PF01652 | 0.652 |
| LIG_FHA_1 | 124 | 130 | PF00498 | 0.667 |
| LIG_FHA_1 | 15 | 21 | PF00498 | 0.650 |
| LIG_FHA_1 | 199 | 205 | PF00498 | 0.809 |
| LIG_FHA_1 | 211 | 217 | PF00498 | 0.634 |
| LIG_FHA_1 | 255 | 261 | PF00498 | 0.768 |
| LIG_FHA_1 | 277 | 283 | PF00498 | 0.538 |
| LIG_FHA_1 | 55 | 61 | PF00498 | 0.797 |
| LIG_FHA_1 | 99 | 105 | PF00498 | 0.797 |
| LIG_FHA_2 | 268 | 274 | PF00498 | 0.734 |
| LIG_FHA_2 | 284 | 290 | PF00498 | 0.478 |
| LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.627 |
| LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.538 |
| LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.702 |
| LIG_PDZ_Class_1 | 311 | 316 | PF00595 | 0.502 |
| LIG_SH2_CRK | 80 | 84 | PF00017 | 0.558 |
| LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.672 |
| LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.657 |
| LIG_SH3_1 | 170 | 176 | PF00018 | 0.777 |
| LIG_SH3_3 | 170 | 176 | PF00018 | 0.724 |
| LIG_SH3_3 | 215 | 221 | PF00018 | 0.573 |
| LIG_SH3_3 | 89 | 95 | PF00018 | 0.708 |
| LIG_SUMO_SIM_anti_2 | 103 | 109 | PF11976 | 0.696 |
| MOD_CDK_SPxxK_3 | 217 | 224 | PF00069 | 0.571 |
| MOD_CK1_1 | 108 | 114 | PF00069 | 0.736 |
| MOD_CK1_1 | 12 | 18 | PF00069 | 0.527 |
| MOD_CK1_1 | 240 | 246 | PF00069 | 0.700 |
| MOD_CK1_1 | 267 | 273 | PF00069 | 0.644 |
| MOD_CK2_1 | 267 | 273 | PF00069 | 0.644 |
| MOD_CK2_1 | 283 | 289 | PF00069 | 0.601 |
| MOD_CK2_1 | 56 | 62 | PF00069 | 0.573 |
| MOD_CK2_1 | 90 | 96 | PF00069 | 0.700 |
| MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.579 |
| MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.718 |
| MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.754 |
| MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.721 |
| MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.803 |
| MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.635 |
| MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.701 |
| MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.742 |
| MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.699 |
| MOD_GSK3_1 | 14 | 21 | PF00069 | 0.767 |
| MOD_GSK3_1 | 176 | 183 | PF00069 | 0.547 |
| MOD_GSK3_1 | 196 | 203 | PF00069 | 0.726 |
| MOD_GSK3_1 | 231 | 238 | PF00069 | 0.712 |
| MOD_GSK3_1 | 240 | 247 | PF00069 | 0.719 |
| MOD_GSK3_1 | 260 | 267 | PF00069 | 0.606 |
| MOD_GSK3_1 | 307 | 314 | PF00069 | 0.696 |
| MOD_GSK3_1 | 54 | 61 | PF00069 | 0.716 |
| MOD_GSK3_1 | 82 | 89 | PF00069 | 0.677 |
| MOD_GSK3_1 | 90 | 97 | PF00069 | 0.717 |
| MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.689 |
| MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.808 |
| MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.713 |
| MOD_N-GLC_2 | 156 | 158 | PF02516 | 0.664 |
| MOD_NEK2_1 | 116 | 121 | PF00069 | 0.651 |
| MOD_NEK2_1 | 200 | 205 | PF00069 | 0.769 |
| MOD_NEK2_1 | 235 | 240 | PF00069 | 0.725 |
| MOD_NEK2_1 | 260 | 265 | PF00069 | 0.527 |
| MOD_NEK2_1 | 283 | 288 | PF00069 | 0.593 |
| MOD_NEK2_1 | 307 | 312 | PF00069 | 0.707 |
| MOD_NEK2_1 | 9 | 14 | PF00069 | 0.711 |
| MOD_PK_1 | 27 | 33 | PF00069 | 0.424 |
| MOD_PKA_2 | 255 | 261 | PF00069 | 0.550 |
| MOD_Plk_1 | 288 | 294 | PF00069 | 0.754 |
| MOD_Plk_4 | 27 | 33 | PF00069 | 0.424 |
| MOD_Plk_4 | 86 | 92 | PF00069 | 0.691 |
| MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.648 |
| MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.600 |
| MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.699 |
| MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.549 |
| MOD_SUMO_rev_2 | 219 | 227 | PF00179 | 0.574 |
| TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.433 |
| TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.639 |
| TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.585 |
| TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.578 |
| TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.559 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HU81 | Leptomonas seymouri | 46% | 100% |
| A0A3S5H6U3 | Leishmania donovani | 69% | 92% |
| A4HWE5 | Leishmania infantum | 69% | 92% |
| E9AQ45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 91% |
| Q4QFD7 | Leishmania major | 67% | 100% |