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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QHE8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 33 | 39 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.539 |
DOC_MAPK_FxFP_2 | 13 | 16 | PF00069 | 0.740 |
DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.765 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.676 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.765 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.816 |
DOC_USP7_UBL2_3 | 106 | 110 | PF12436 | 0.711 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.712 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.675 |
LIG_Clathr_ClatBox_1 | 257 | 261 | PF01394 | 0.438 |
LIG_CSL_BTD_1 | 6 | 9 | PF09270 | 0.628 |
LIG_deltaCOP1_diTrp_1 | 160 | 168 | PF00928 | 0.322 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.388 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.770 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.324 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.802 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.722 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 186 | 197 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 277 | 282 | PF02991 | 0.529 |
LIG_Pex14_1 | 231 | 235 | PF04695 | 0.385 |
LIG_PTB_Apo_2 | 231 | 238 | PF02174 | 0.519 |
LIG_PTB_Phospho_1 | 231 | 237 | PF10480 | 0.519 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.557 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.663 |
LIG_SH2_NCK_1 | 136 | 140 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.547 |
LIG_SUMO_SIM_anti_2 | 268 | 275 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 268 | 275 | PF11976 | 0.304 |
LIG_TRFH_1 | 265 | 269 | PF08558 | 0.382 |
LIG_TYR_ITIM | 52 | 57 | PF00017 | 0.606 |
LIG_WRC_WIRS_1 | 181 | 186 | PF05994 | 0.324 |
LIG_WRC_WIRS_1 | 273 | 278 | PF05994 | 0.515 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.614 |
MOD_CDK_SPxK_1 | 5 | 11 | PF00069 | 0.605 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.438 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.441 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.763 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.440 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.587 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.689 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.816 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.438 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.735 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.716 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.316 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.424 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.433 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.539 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.438 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.766 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.302 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.494 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.742 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.492 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.815 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.710 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.306 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.329 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.279 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.204 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.440 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.594 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.691 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.634 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.759 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.350 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.260 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.510 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.750 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.723 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.321 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.733 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.763 |
TRG_DiLeu_BaEn_4 | 160 | 166 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.685 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.762 |
TRG_Pf-PMV_PEXEL_1 | 123 | 127 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILE4 | Leptomonas seymouri | 58% | 84% |
A0A0S4ILW7 | Bodo saltans | 49% | 93% |
A0A1X0NQ98 | Trypanosomatidae | 60% | 100% |
A0A3S5IS56 | Trypanosoma rangeli | 57% | 100% |
A0A3S7WR67 | Leishmania donovani | 92% | 100% |
A4H659 | Leishmania braziliensis | 78% | 85% |
A4HUH9 | Leishmania infantum | 92% | 100% |
C9ZVK4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AN77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BP48 | Trypanosoma cruzi | 53% | 100% |