A Kinetoplastid-specific signal-anchored protein. Might be part of a bigger complex.
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S7XA27
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.591 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.604 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.379 |
CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.416 |
DEG_SCF_FBW7_1 | 307 | 312 | PF00400 | 0.354 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.529 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 43 | 52 | PF00134 | 0.330 |
DOC_MAPK_DCC_7 | 10 | 19 | PF00069 | 0.482 |
DOC_MAPK_DCC_7 | 275 | 283 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 275 | 283 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 275 | 283 | PF00069 | 0.340 |
DOC_PP4_FxxP_1 | 166 | 169 | PF00568 | 0.313 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.278 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.450 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.581 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.358 |
LIG_Actin_WH2_2 | 318 | 333 | PF00022 | 0.407 |
LIG_APCC_ABBA_1 | 229 | 234 | PF00400 | 0.322 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.579 |
LIG_BRCT_BRCA1_1 | 162 | 166 | PF00533 | 0.499 |
LIG_deltaCOP1_diTrp_1 | 298 | 304 | PF00928 | 0.387 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.412 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.381 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.319 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.402 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.559 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.419 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.467 |
LIG_LIR_Apic_2 | 163 | 169 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 64 | 69 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.343 |
LIG_PCNA_yPIPBox_3 | 133 | 141 | PF02747 | 0.335 |
LIG_Pex14_1 | 300 | 304 | PF04695 | 0.346 |
LIG_Pex14_2 | 19 | 23 | PF04695 | 0.319 |
LIG_Rb_LxCxE_1 | 328 | 342 | PF01857 | 0.450 |
LIG_REV1ctd_RIR_1 | 261 | 270 | PF16727 | 0.360 |
LIG_REV1ctd_RIR_1 | 6 | 14 | PF16727 | 0.585 |
LIG_RPA_C_Fungi | 208 | 220 | PF08784 | 0.334 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.533 |
LIG_SH3_1 | 141 | 147 | PF00018 | 0.513 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.507 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.593 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.489 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.326 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 226 | 234 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.533 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.531 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.363 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.376 |
LIG_UBA3_1 | 76 | 82 | PF00899 | 0.546 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.505 |
MOD_CDC14_SPxK_1 | 224 | 227 | PF00782 | 0.416 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.426 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.696 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.536 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.621 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.324 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.554 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.339 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.499 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.458 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.401 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.609 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.448 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.737 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.649 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.675 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.485 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.482 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.625 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.499 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.418 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.442 |
MOD_PK_1 | 72 | 78 | PF00069 | 0.410 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.462 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.500 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.343 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.497 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.383 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.475 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.397 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.506 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.444 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.516 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.639 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.622 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.470 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.537 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.481 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.537 |
TRG_DiLeu_BaEn_1 | 30 | 35 | PF01217 | 0.414 |
TRG_DiLeu_BaLyEn_6 | 276 | 281 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2I6 | Leptomonas seymouri | 62% | 97% |
A0A0S4J6X6 | Bodo saltans | 32% | 100% |
A0A0S4J7W0 | Bodo saltans | 32% | 100% |
A0A1X0P4T2 | Trypanosomatidae | 37% | 100% |
A0A3R7MCD3 | Trypanosoma rangeli | 42% | 100% |
A4HNG0 | Leishmania braziliensis | 79% | 100% |
A4IC71 | Leishmania infantum | 100% | 100% |
C9ZYG3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AFX1 | Leishmania major | 94% | 100% |
E9B724 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5B4K6 | Trypanosoma cruzi | 40% | 100% |