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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S7X062
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.653 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.364 |
CLV_PCSK_FUR_1 | 38 | 42 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 40 | 42 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.454 |
CLV_Separin_Metazoa | 75 | 79 | PF03568 | 0.499 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.351 |
DOC_MAPK_DCC_7 | 193 | 202 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 193 | 202 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 222 | 229 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 193 | 202 | PF00069 | 0.525 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.426 |
DOC_USP7_UBL2_3 | 136 | 140 | PF12436 | 0.606 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.523 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 209 | 218 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 222 | 231 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 99 | 106 | PF00244 | 0.502 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.543 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.539 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.647 |
LIG_LIR_Apic_2 | 192 | 198 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 216 | 221 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.624 |
LIG_PCNA_yPIPBox_3 | 25 | 39 | PF02747 | 0.526 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.680 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.428 |
LIG_SH2_GRB2like | 67 | 70 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.466 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.481 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.554 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 187 | 190 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.440 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.537 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.564 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.458 |
LIG_TYR_ITIM | 31 | 36 | PF00017 | 0.547 |
MOD_CDK_SPK_2 | 161 | 166 | PF00069 | 0.780 |
MOD_CDK_SPK_2 | 94 | 99 | PF00069 | 0.556 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.773 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.537 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.517 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.502 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.713 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.677 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.602 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.596 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.522 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.749 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.403 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.619 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.572 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.514 |
MOD_N-GLC_2 | 186 | 188 | PF02516 | 0.470 |
MOD_N-GLC_2 | 69 | 71 | PF02516 | 0.423 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.618 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.452 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.637 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.627 |
MOD_PK_1 | 196 | 202 | PF00069 | 0.534 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.656 |
MOD_PKA_1 | 222 | 228 | PF00069 | 0.607 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.683 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.609 |
MOD_PKB_1 | 230 | 238 | PF00069 | 0.654 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.663 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.573 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.520 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.660 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.404 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.739 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.421 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.603 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.561 |
MOD_SUMO_for_1 | 141 | 144 | PF00179 | 0.640 |
TRG_DiLeu_BaEn_3 | 95 | 101 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_4 | 263 | 269 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.657 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.537 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.450 |
TRG_NLS_MonoExtN_4 | 272 | 279 | PF00514 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 209 | 214 | PF00026 | 0.647 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P3 | Leptomonas seymouri | 65% | 100% |
A0A0S4J034 | Bodo saltans | 27% | 100% |
A0A1X0P7J6 | Trypanosomatidae | 35% | 100% |
A0A3R7NVA4 | Trypanosoma rangeli | 32% | 100% |
A4HF76 | Leishmania braziliensis | 85% | 100% |
A4I2F9 | Leishmania infantum | 100% | 100% |
C9ZX38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AYL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q8W0 | Leishmania major | 95% | 100% |
V5D9J1 | Trypanosoma cruzi | 34% | 100% |