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: E9B724
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.677 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.642 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.427 |
CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.440 |
DEG_SCF_FBW7_1 | 307 | 312 | PF00400 | 0.453 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.569 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 43 | 52 | PF00134 | 0.378 |
DOC_MAPK_DCC_7 | 10 | 19 | PF00069 | 0.520 |
DOC_MAPK_DCC_7 | 275 | 283 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 275 | 283 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 275 | 283 | PF00069 | 0.370 |
DOC_MAPK_RevD_3 | 260 | 276 | PF00069 | 0.273 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.392 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.629 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.448 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 293 | 300 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 336 | 342 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 318 | 333 | PF00022 | 0.418 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.639 |
LIG_deltaCOP1_diTrp_1 | 298 | 304 | PF00928 | 0.408 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.524 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.415 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.355 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.425 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.431 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.591 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.450 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.473 |
LIG_LIR_Apic_2 | 64 | 69 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 185 | 196 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.372 |
LIG_PCNA_yPIPBox_3 | 133 | 141 | PF02747 | 0.432 |
LIG_Pex14_1 | 300 | 304 | PF04695 | 0.379 |
LIG_Pex14_2 | 19 | 23 | PF04695 | 0.337 |
LIG_Rb_LxCxE_1 | 328 | 348 | PF01857 | 0.477 |
LIG_REV1ctd_RIR_1 | 261 | 270 | PF16727 | 0.377 |
LIG_REV1ctd_RIR_1 | 6 | 14 | PF16727 | 0.632 |
LIG_RPA_C_Fungi | 208 | 220 | PF08784 | 0.406 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.565 |
LIG_SH3_1 | 141 | 147 | PF00018 | 0.625 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.577 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.643 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.509 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.558 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.567 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.445 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.438 |
LIG_UBA3_1 | 76 | 82 | PF00899 | 0.568 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.539 |
MOD_CDC14_SPxK_1 | 224 | 227 | PF00782 | 0.541 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.555 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.690 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.380 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.690 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.423 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.559 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.391 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.538 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.525 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.449 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.618 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.637 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.768 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.752 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.684 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.698 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.710 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.528 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.530 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.636 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.511 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.525 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.416 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.577 |
MOD_PK_1 | 72 | 78 | PF00069 | 0.500 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.273 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.553 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.518 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.397 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.520 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.522 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.506 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.551 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.468 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.566 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.704 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.656 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.503 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.565 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.564 |
TRG_DiLeu_BaEn_1 | 30 | 35 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 276 | 281 | PF01217 | 0.649 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 74 | 78 | PF00026 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2I6 | Leptomonas seymouri | 61% | 99% |
A0A0S4J6X6 | Bodo saltans | 34% | 100% |
A0A0S4J7W0 | Bodo saltans | 32% | 100% |
A0A1X0P4T2 | Trypanosomatidae | 38% | 100% |
A0A3R7MCD3 | Trypanosoma rangeli | 41% | 100% |
A0A3S7XA27 | Leishmania donovani | 92% | 100% |
A4HNG0 | Leishmania braziliensis | 78% | 100% |
A4IC71 | Leishmania infantum | 92% | 100% |
C9ZYG3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AFX1 | Leishmania major | 91% | 100% |
V5B4K6 | Trypanosoma cruzi | 40% | 100% |