| 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: A0A3S7X1G1
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.787 | 
| CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.660 | 
| CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.649 | 
| CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.757 | 
| CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.641 | 
| CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.772 | 
| CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.799 | 
| CLV_NRD_NRD_1 | 350 | 352 | PF00675 | 0.718 | 
| CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.566 | 
| CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.675 | 
| CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.755 | 
| CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.660 | 
| CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.689 | 
| CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.756 | 
| CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.616 | 
| CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.676 | 
| CLV_PCSK_KEX2_1 | 350 | 352 | PF00082 | 0.718 | 
| CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.566 | 
| CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.678 | 
| CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.717 | 
| CLV_PCSK_PC7_1 | 15 | 21 | PF00082 | 0.691 | 
| CLV_PCSK_PC7_1 | 239 | 245 | PF00082 | 0.603 | 
| DEG_COP1_1 | 130 | 137 | PF00400 | 0.712 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.668 | 
| DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.748 | 
| DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.791 | 
| DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.653 | 
| DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.815 | 
| DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.734 | 
| DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.740 | 
| DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.831 | 
| DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.765 | 
| DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.716 | 
| DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.724 | 
| DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.814 | 
| LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.752 | 
| LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.735 | 
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.658 | 
| LIG_FHA_1 | 176 | 182 | PF00498 | 0.832 | 
| LIG_FHA_1 | 5 | 11 | PF00498 | 0.757 | 
| LIG_FHA_2 | 134 | 140 | PF00498 | 0.670 | 
| LIG_LIR_Apic_2 | 255 | 261 | PF02991 | 0.730 | 
| LIG_LIR_Gen_1 | 154 | 163 | PF02991 | 0.670 | 
| LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.661 | 
| LIG_SH2_GRB2like | 302 | 305 | PF00017 | 0.718 | 
| LIG_SH2_SRC | 302 | 305 | PF00017 | 0.718 | 
| LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.739 | 
| LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.726 | 
| LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.681 | 
| LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.669 | 
| LIG_SH3_1 | 201 | 207 | PF00018 | 0.693 | 
| LIG_SH3_3 | 201 | 207 | PF00018 | 0.695 | 
| LIG_SH3_3 | 42 | 48 | PF00018 | 0.756 | 
| LIG_SH3_4 | 284 | 291 | PF00018 | 0.738 | 
| LIG_WW_1 | 293 | 296 | PF00397 | 0.623 | 
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.750 | 
| MOD_CK1_1 | 289 | 295 | PF00069 | 0.636 | 
| MOD_CK2_1 | 220 | 226 | PF00069 | 0.810 | 
| MOD_CK2_1 | 306 | 312 | PF00069 | 0.606 | 
| MOD_CK2_1 | 374 | 380 | PF00069 | 0.735 | 
| MOD_Cter_Amidation | 208 | 211 | PF01082 | 0.755 | 
| MOD_Cter_Amidation | 22 | 25 | PF01082 | 0.629 | 
| MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.739 | 
| MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.798 | 
| MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.769 | 
| MOD_GlcNHglycan | 226 | 230 | PF01048 | 0.814 | 
| MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.652 | 
| MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.718 | 
| MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.776 | 
| MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.586 | 
| MOD_GSK3_1 | 147 | 154 | PF00069 | 0.677 | 
| MOD_GSK3_1 | 175 | 182 | PF00069 | 0.832 | 
| MOD_GSK3_1 | 215 | 222 | PF00069 | 0.765 | 
| MOD_GSK3_1 | 306 | 313 | PF00069 | 0.673 | 
| MOD_GSK3_1 | 78 | 85 | PF00069 | 0.816 | 
| MOD_GSK3_1 | 97 | 104 | PF00069 | 0.507 | 
| MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.656 | 
| MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.760 | 
| MOD_NEK2_1 | 195 | 200 | PF00069 | 0.608 | 
| MOD_NEK2_1 | 34 | 39 | PF00069 | 0.573 | 
| MOD_NEK2_1 | 361 | 366 | PF00069 | 0.735 | 
| MOD_PIKK_1 | 122 | 128 | PF00454 | 0.750 | 
| MOD_PKA_1 | 19 | 25 | PF00069 | 0.643 | 
| MOD_PKA_1 | 87 | 93 | PF00069 | 0.725 | 
| MOD_PKA_2 | 122 | 128 | PF00069 | 0.744 | 
| MOD_PKA_2 | 19 | 25 | PF00069 | 0.636 | 
| MOD_PKA_2 | 305 | 311 | PF00069 | 0.782 | 
| MOD_PKA_2 | 87 | 93 | PF00069 | 0.684 | 
| MOD_Plk_1 | 219 | 225 | PF00069 | 0.735 | 
| MOD_Plk_1 | 362 | 368 | PF00069 | 0.701 | 
| MOD_Plk_4 | 63 | 69 | PF00069 | 0.617 | 
| MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.833 | 
| MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.766 | 
| MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.716 | 
| MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.725 | 
| MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.813 | 
| TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.770 | 
| TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.612 | 
| TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.825 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P454 | Leptomonas seymouri | 40% | 100% | 
| A4HGF0 | Leishmania braziliensis | 61% | 100% | 
| A4I3I1 | Leishmania infantum | 99% | 100% | 
| E9AZS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% | 
| Q4Q8G1 | Leishmania major | 91% | 100% |