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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9ALV6
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.665 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.508 |
CLV_MEL_PAP_1 | 140 | 146 | PF00089 | 0.628 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.631 |
CLV_PCSK_FUR_1 | 158 | 162 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.454 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.619 |
DEG_SPOP_SBC_1 | 169 | 173 | PF00917 | 0.589 |
DOC_AGCK_PIF_1 | 350 | 355 | PF00069 | 0.365 |
DOC_CKS1_1 | 272 | 277 | PF01111 | 0.574 |
DOC_MAPK_gen_1 | 31 | 38 | PF00069 | 0.406 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.638 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.569 |
DOC_USP7_MATH_2 | 46 | 52 | PF00917 | 0.468 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 158 | 168 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 188 | 194 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 98 | 107 | PF00244 | 0.445 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.637 |
LIG_CaM_IQ_9 | 50 | 66 | PF13499 | 0.503 |
LIG_Clathr_ClatBox_1 | 44 | 48 | PF01394 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 345 | 353 | PF00928 | 0.374 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.605 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.625 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.599 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.344 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.487 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.606 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.618 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.304 |
LIG_LIR_Apic_2 | 78 | 83 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 297 | 304 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 345 | 355 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 39 | 47 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 351 | 356 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.724 |
LIG_NRBOX | 123 | 129 | PF00104 | 0.444 |
LIG_PALB2_WD40_1 | 294 | 302 | PF16756 | 0.420 |
LIG_PTAP_UEV_1 | 238 | 243 | PF05743 | 0.582 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.503 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.539 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.606 |
LIG_SH2_GRB2like | 226 | 229 | PF00017 | 0.448 |
LIG_SH2_GRB2like | 80 | 83 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 226 | 230 | PF00017 | 0.451 |
LIG_SH2_SRC | 226 | 229 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.484 |
LIG_SH3_2 | 239 | 244 | PF14604 | 0.622 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.668 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.471 |
LIG_SUMO_SIM_par_1 | 308 | 314 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 333 | 338 | PF11976 | 0.412 |
LIG_SxIP_EBH_1 | 170 | 182 | PF03271 | 0.468 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.602 |
LIG_TRAF2_1 | 291 | 294 | PF00917 | 0.497 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.240 |
LIG_TRAF2_1 | 87 | 90 | PF00917 | 0.345 |
LIG_UBA3_1 | 22 | 31 | PF00899 | 0.404 |
MOD_CDK_SPK_2 | 205 | 210 | PF00069 | 0.620 |
MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.438 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.759 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.718 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.649 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.602 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.587 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.696 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.474 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.440 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.614 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.706 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.673 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.667 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.324 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.553 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.661 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.662 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.624 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.596 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.697 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.598 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.626 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.395 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.510 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.561 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.768 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.479 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.741 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.608 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.458 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.468 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.594 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.647 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.615 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.648 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.451 |
MOD_PKB_1 | 158 | 166 | PF00069 | 0.566 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.498 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.547 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.666 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.465 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.447 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.311 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.442 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.616 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.637 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.671 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 192 | 201 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_2 | 350 | 356 | PF01217 | 0.228 |
TRG_DiLeu_BaEn_2 | 47 | 53 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.592 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7W0 | Leptomonas seymouri | 47% | 100% |
A0A1X0NZT2 | Trypanosomatidae | 31% | 100% |
A0A3Q8IRA6 | Leishmania donovani | 86% | 98% |
A0A3R7NQI4 | Trypanosoma rangeli | 30% | 100% |
A4HHC9 | Leishmania braziliensis | 70% | 100% |
A4I4H4 | Leishmania infantum | 86% | 98% |
E9ADX5 | Leishmania major | 85% | 100% |