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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALC9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.655 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.550 |
CLV_PCSK_FUR_1 | 69 | 73 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 293 | 299 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.515 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.723 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.722 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 94 | 104 | PF00244 | 0.644 |
LIG_Actin_WH2_2 | 55 | 73 | PF00022 | 0.615 |
LIG_BIR_III_4 | 200 | 204 | PF00653 | 0.601 |
LIG_CaM_NSCaTE_8 | 235 | 242 | PF13499 | 0.555 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.627 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.662 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.676 |
LIG_GBD_Chelix_1 | 129 | 137 | PF00786 | 0.637 |
LIG_LIR_Apic_2 | 147 | 151 | PF02991 | 0.591 |
LIG_PTB_Apo_2 | 138 | 145 | PF02174 | 0.504 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.425 |
LIG_SUMO_SIM_par_1 | 55 | 60 | PF11976 | 0.632 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.622 |
LIG_WRC_WIRS_1 | 250 | 255 | PF05994 | 0.405 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.660 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.619 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.611 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.417 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.564 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.672 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.663 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.601 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.679 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.644 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.610 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.594 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.425 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.647 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.542 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.561 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.600 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.507 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.640 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.677 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.582 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.552 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.764 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.615 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.670 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.539 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.610 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.478 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.683 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.565 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.678 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.775 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.564 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.545 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.591 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.726 |
MOD_SUMO_rev_2 | 198 | 206 | PF00179 | 0.612 |
MOD_SUMO_rev_2 | 261 | 268 | PF00179 | 0.626 |
TRG_ER_diArg_1 | 172 | 174 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.549 |
TRG_NLS_Bipartite_1 | 173 | 188 | PF00514 | 0.743 |
TRG_NLS_MonoExtN_4 | 181 | 188 | PF00514 | 0.744 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.711 |
TRG_Pf-PMV_PEXEL_1 | 72 | 76 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3L7 | Leptomonas seymouri | 57% | 100% |
A0A1X0NPM5 | Trypanosomatidae | 29% | 91% |
A0A3R7LS50 | Trypanosoma rangeli | 34% | 100% |
A0A3S5H619 | Leishmania donovani | 87% | 100% |
A4H559 | Leishmania braziliensis | 73% | 100% |
A4HTD6 | Leishmania infantum | 87% | 100% |
C9ZUH8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4QIH6 | Leishmania major | 86% | 100% |
V5BYD2 | Trypanosoma cruzi | 34% | 90% |