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 | 10 |
GO:0020016 | ciliary pocket | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q8C7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.737 |
CLV_C14_Caspase3-7 | 253 | 257 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 76 | 78 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.417 |
DEG_MDM2_SWIB_1 | 141 | 149 | PF02201 | 0.419 |
DOC_CKS1_1 | 69 | 74 | PF01111 | 0.719 |
DOC_CYCLIN_RxL_1 | 50 | 60 | PF00134 | 0.619 |
DOC_MAPK_gen_1 | 275 | 282 | PF00069 | 0.572 |
DOC_MAPK_HePTP_8 | 127 | 139 | PF00069 | 0.623 |
DOC_MAPK_MEF2A_6 | 130 | 139 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 275 | 284 | PF00069 | 0.560 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.741 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 36 | 42 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 64 | 69 | PF00244 | 0.762 |
LIG_Actin_WH2_2 | 215 | 230 | PF00022 | 0.406 |
LIG_CaM_IQ_9 | 186 | 202 | PF13499 | 0.324 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.681 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.500 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.316 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.688 |
LIG_GBD_Chelix_1 | 282 | 290 | PF00786 | 0.437 |
LIG_Integrin_isoDGR_2 | 260 | 262 | PF01839 | 0.229 |
LIG_Integrin_RGD_1 | 77 | 79 | PF01839 | 0.530 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 326 | 336 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.279 |
LIG_PALB2_WD40_1 | 324 | 332 | PF16756 | 0.253 |
LIG_PDZ_Class_1 | 337 | 342 | PF00595 | 0.441 |
LIG_Pex14_2 | 141 | 145 | PF04695 | 0.390 |
LIG_SH2_GRB2like | 240 | 243 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 33 | 37 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.437 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.510 |
LIG_SUMO_SIM_anti_2 | 158 | 164 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 206 | 213 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.229 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.713 |
LIG_WW_3 | 40 | 44 | PF00397 | 0.636 |
MOD_CDC14_SPxK_1 | 236 | 239 | PF00782 | 0.523 |
MOD_CDC14_SPxK_1 | 73 | 76 | PF00782 | 0.704 |
MOD_CDK_SPxK_1 | 233 | 239 | PF00069 | 0.523 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.751 |
MOD_CDK_SPxxK_3 | 70 | 77 | PF00069 | 0.752 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.424 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.385 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.359 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.735 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.730 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.698 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.687 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.509 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.476 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.606 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.587 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.382 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.548 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.454 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.648 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.679 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.813 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.363 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.310 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.395 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.750 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.319 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.780 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.768 |
MOD_LATS_1 | 233 | 239 | PF00433 | 0.500 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.327 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.382 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.310 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.334 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.633 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.743 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.336 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.753 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.618 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.366 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.798 |
MOD_PKB_1 | 119 | 127 | PF00069 | 0.685 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.788 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.477 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.529 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.289 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.405 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.564 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.739 |
MOD_SUMO_for_1 | 57 | 60 | PF00179 | 0.720 |
TRG_DiLeu_BaLyEn_6 | 51 | 56 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.702 |
TRG_NLS_Bipartite_1 | 76 | 98 | PF00514 | 0.725 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7I8 | Leptomonas seymouri | 44% | 100% |
A0A1X0NYN9 | Trypanosomatidae | 41% | 100% |
A0A3S7X1H6 | Leishmania donovani | 92% | 100% |
A4HDI3 | Leishmania braziliensis | 26% | 100% |
A4HGJ1 | Leishmania braziliensis | 63% | 100% |
A4I0W6 | Leishmania infantum | 24% | 100% |
A4I3L8 | Leishmania infantum | 92% | 100% |
E9AZV8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
V5AQB9 | Trypanosoma cruzi | 36% | 100% |