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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7WYL9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 72 | 76 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.715 |
CLV_PCSK_PC7_1 | 294 | 300 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.440 |
DOC_CKS1_1 | 235 | 240 | PF01111 | 0.740 |
DOC_MAPK_DCC_7 | 279 | 288 | PF00069 | 0.698 |
DOC_MAPK_gen_1 | 279 | 288 | PF00069 | 0.698 |
DOC_MAPK_MEF2A_6 | 279 | 288 | PF00069 | 0.698 |
DOC_MAPK_MEF2A_6 | 91 | 100 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.704 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.743 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.771 |
LIG_14-3-3_CanoR_1 | 121 | 126 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 208 | 217 | PF00244 | 0.711 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.597 |
LIG_Clathr_ClatBox_1 | 125 | 129 | PF01394 | 0.544 |
LIG_eIF4E_1 | 84 | 90 | PF01652 | 0.373 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.678 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.560 |
LIG_Integrin_isoDGR_2 | 242 | 244 | PF01839 | 0.668 |
LIG_LIR_Apic_2 | 232 | 238 | PF02991 | 0.732 |
LIG_LIR_Gen_1 | 134 | 143 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 187 | 195 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 59 | 69 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 187 | 192 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.438 |
LIG_NRBOX | 159 | 165 | PF00104 | 0.606 |
LIG_PALB2_WD40_1 | 123 | 131 | PF16756 | 0.537 |
LIG_PTAP_UEV_1 | 226 | 231 | PF05743 | 0.597 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.526 |
LIG_SH2_CRK | 235 | 239 | PF00017 | 0.770 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.594 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.380 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.676 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.615 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.797 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 213 | 220 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 213 | 220 | PF11976 | 0.544 |
LIG_TYR_ITIM | 28 | 33 | PF00017 | 0.531 |
MOD_CDK_SPK_2 | 12 | 17 | PF00069 | 0.715 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.760 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.464 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.510 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.482 |
MOD_Cter_Amidation | 296 | 299 | PF01082 | 0.762 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.440 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.414 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.389 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.721 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.784 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.754 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.643 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.452 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.558 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.736 |
MOD_LATS_1 | 206 | 212 | PF00433 | 0.606 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.487 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.523 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.718 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.782 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.522 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.620 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.491 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.558 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.697 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.658 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.661 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.796 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.544 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.770 |
MOD_SUMO_rev_2 | 218 | 224 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_1 | 159 | 164 | PF01217 | 0.605 |
TRG_DiLeu_BaLyEn_6 | 101 | 106 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.527 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.612 |
TRG_NES_CRM1_1 | 123 | 136 | PF08389 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R9 | Leptomonas seymouri | 65% | 100% |
A0A1X0NWE2 | Trypanosomatidae | 39% | 100% |
A0A3R7MR43 | Trypanosoma rangeli | 38% | 100% |
A4HDS1 | Leishmania braziliensis | 86% | 100% |
A4I119 | Leishmania infantum | 99% | 100% |
C9ZW91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AX56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QAC0 | Leishmania major | 95% | 100% |
V5AV25 | Trypanosoma cruzi | 41% | 100% |