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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9B3W2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.589 |
CLV_PCSK_FUR_1 | 262 | 266 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.451 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.683 |
CLV_Separin_Metazoa | 121 | 125 | PF03568 | 0.353 |
DOC_ANK_TNKS_1 | 114 | 121 | PF00023 | 0.342 |
DOC_ANK_TNKS_1 | 123 | 130 | PF00023 | 0.332 |
DOC_MAPK_gen_1 | 236 | 246 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 254 | 263 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 254 | 263 | PF00069 | 0.649 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.406 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.614 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.550 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 27 | 32 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 289 | 297 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.366 |
LIG_Actin_WH2_2 | 119 | 136 | PF00022 | 0.409 |
LIG_AP2alpha_2 | 258 | 260 | PF02296 | 0.618 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.341 |
LIG_deltaCOP1_diTrp_1 | 258 | 266 | PF00928 | 0.621 |
LIG_eIF4E_1 | 217 | 223 | PF01652 | 0.419 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.355 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.427 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.415 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.572 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.382 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.374 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.405 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.409 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.603 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.386 |
LIG_LIR_Apic_2 | 299 | 305 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.625 |
LIG_LIR_LC3C_4 | 220 | 224 | PF02991 | 0.187 |
LIG_LIR_Nem_3 | 137 | 142 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.548 |
LIG_SH2_GRB2like | 209 | 212 | PF00017 | 0.449 |
LIG_SH2_SRC | 209 | 212 | PF00017 | 0.449 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.339 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 21 | 27 | PF11976 | 0.369 |
LIG_SUMO_SIM_anti_2 | 220 | 226 | PF11976 | 0.187 |
LIG_SUMO_SIM_anti_2 | 98 | 106 | PF11976 | 0.280 |
LIG_SUMO_SIM_par_1 | 43 | 48 | PF11976 | 0.495 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.616 |
LIG_UBA3_1 | 174 | 179 | PF00899 | 0.361 |
LIG_WW_1 | 167 | 170 | PF00397 | 0.288 |
LIG_WW_3 | 74 | 78 | PF00397 | 0.464 |
MOD_CDC14_SPxK_1 | 205 | 208 | PF00782 | 0.387 |
MOD_CDC14_SPxK_1 | 31 | 34 | PF00782 | 0.360 |
MOD_CDK_SPxK_1 | 202 | 208 | PF00069 | 0.390 |
MOD_CDK_SPxK_1 | 28 | 34 | PF00069 | 0.359 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.469 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.607 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.653 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.554 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.399 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.512 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.393 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.419 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.613 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.410 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.736 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.456 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.693 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.657 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.755 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.382 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.387 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.187 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.618 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.524 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.383 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.588 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.388 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.687 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.489 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.472 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.543 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.650 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.469 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.638 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.607 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.614 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.508 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.684 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.331 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.673 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.384 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.364 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.315 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.398 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.359 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.475 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.540 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4F7 | Leptomonas seymouri | 81% | 100% |
A0A0S4JAA8 | Bodo saltans | 56% | 100% |
A0A1X0P101 | Trypanosomatidae | 74% | 99% |
A0A3Q8IHR6 | Leishmania donovani | 92% | 100% |
A4HLI3 | Leishmania braziliensis | 88% | 100% |
A4I8Z3 | Leishmania infantum | 92% | 100% |
D0A4Z1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
Q4Q462 | Leishmania major | 92% | 100% |