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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 8 |
GO:0042995 | cell projection | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 8 |
Related structures:
AlphaFold database: E9AD57
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.371 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.754 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.473 |
DOC_CYCLIN_RxL_1 | 197 | 208 | PF00134 | 0.427 |
DOC_CYCLIN_RxL_1 | 264 | 275 | PF00134 | 0.355 |
DOC_MAPK_MEF2A_6 | 213 | 220 | PF00069 | 0.460 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.426 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.783 |
LIG_14-3-3_CanoR_1 | 138 | 146 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 171 | 176 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 64 | 70 | PF00244 | 0.596 |
LIG_14-3-3_CterR_2 | 347 | 352 | PF00244 | 0.445 |
LIG_Actin_WH2_2 | 262 | 280 | PF00022 | 0.417 |
LIG_AP2alpha_1 | 262 | 266 | PF02296 | 0.341 |
LIG_Clathr_ClatBox_1 | 172 | 176 | PF01394 | 0.321 |
LIG_Clathr_ClatBox_1 | 217 | 221 | PF01394 | 0.385 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.505 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.388 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.545 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.501 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.552 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.406 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.359 |
LIG_GBD_Chelix_1 | 269 | 277 | PF00786 | 0.378 |
LIG_LIR_Gen_1 | 166 | 177 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.484 |
LIG_NRBOX | 200 | 206 | PF00104 | 0.403 |
LIG_Pex14_2 | 262 | 266 | PF04695 | 0.341 |
LIG_Rb_LxCxE_1 | 174 | 192 | PF01857 | 0.371 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.397 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 214 | 222 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 214 | 222 | PF11976 | 0.317 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.443 |
LIG_WW_3 | 61 | 65 | PF00397 | 0.573 |
MOD_CDC14_SPxK_1 | 152 | 155 | PF00782 | 0.454 |
MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.430 |
MOD_CDK_SPxK_1 | 58 | 64 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 58 | 65 | PF00069 | 0.712 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.593 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.534 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.767 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.650 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.418 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.537 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.710 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.712 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.650 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.511 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.447 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.543 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.631 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.553 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.492 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.399 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.509 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.398 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.426 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.488 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.495 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.445 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.255 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.388 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.395 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.542 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.520 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.501 |
MOD_NEK2_2 | 249 | 254 | PF00069 | 0.527 |
MOD_NEK2_2 | 311 | 316 | PF00069 | 0.313 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.544 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.526 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.388 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.654 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.358 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.783 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.446 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.422 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.395 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.433 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.388 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.356 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.480 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.549 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.507 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.786 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 200 | 205 | PF01217 | 0.298 |
TRG_DiLeu_LyEn_5 | 327 | 332 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.690 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0A7 | Leptomonas seymouri | 40% | 99% |
A0A1X0NS64 | Trypanosomatidae | 27% | 100% |
A0A3S7X0J8 | Leishmania donovani | 89% | 100% |
A4HFK3 | Leishmania braziliensis | 67% | 98% |
E9AHF2 | Leishmania infantum | 89% | 89% |
E9AYY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |