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: A4HNG0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.670 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.663 |
CLV_PCSK_PC7_1 | 212 | 218 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.414 |
CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.437 |
DEG_SCF_FBW7_1 | 306 | 311 | PF00400 | 0.457 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.512 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 43 | 52 | PF00134 | 0.371 |
DOC_MAPK_DCC_7 | 10 | 19 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 7 | 19 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.522 |
DOC_MAPK_RevD_3 | 320 | 336 | PF00069 | 0.269 |
DOC_PP1_RVXF_1 | 4 | 10 | PF00149 | 0.583 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.406 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.392 |
LIG_Actin_WH2_2 | 314 | 332 | PF00022 | 0.429 |
LIG_APCC_ABBA_1 | 228 | 233 | PF00400 | 0.358 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.629 |
LIG_deltaCOP1_diTrp_1 | 297 | 303 | PF00928 | 0.408 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.514 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.428 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.420 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.430 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.404 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.450 |
LIG_LIR_Apic_2 | 64 | 69 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 130 | 139 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 166 | 171 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 94 | 103 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.369 |
LIG_PCNA_yPIPBox_3 | 133 | 141 | PF02747 | 0.423 |
LIG_Pex14_1 | 299 | 303 | PF04695 | 0.383 |
LIG_Pex14_2 | 19 | 23 | PF04695 | 0.337 |
LIG_Rb_LxCxE_1 | 327 | 344 | PF01857 | 0.473 |
LIG_REV1ctd_RIR_1 | 260 | 269 | PF16727 | 0.379 |
LIG_REV1ctd_RIR_1 | 6 | 14 | PF16727 | 0.617 |
LIG_RPA_C_Fungi | 207 | 219 | PF08784 | 0.406 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.580 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.612 |
LIG_SH2_NCK_1 | 4 | 8 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.565 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.517 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.657 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.381 |
LIG_SUMO_SIM_anti_2 | 75 | 81 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.564 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.559 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.464 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.422 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.522 |
MOD_CDC14_SPxK_1 | 223 | 226 | PF00782 | 0.542 |
MOD_CDK_SPxK_1 | 220 | 226 | PF00069 | 0.556 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.511 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.561 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.391 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.514 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.448 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.620 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.350 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.544 |
MOD_GlcNHglycan | 30 | 34 | PF01048 | 0.558 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.642 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.680 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.608 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.535 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.564 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.543 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.670 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.538 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.551 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.519 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.417 |
MOD_NEK2_2 | 257 | 262 | PF00069 | 0.252 |
MOD_NEK2_2 | 69 | 74 | PF00069 | 0.496 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.688 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.576 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.555 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.443 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.520 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.397 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.535 |
MOD_Plk_2-3 | 113 | 119 | PF00069 | 0.437 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.522 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.631 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.546 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.473 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.476 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.554 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.663 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.504 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.572 |
TRG_DiLeu_BaEn_1 | 30 | 35 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.390 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.581 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.548 |
TRG_NES_CRM1_1 | 323 | 338 | PF08389 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2I6 | Leptomonas seymouri | 60% | 99% |
A0A0S4J6X6 | Bodo saltans | 32% | 100% |
A0A0S4J7W0 | Bodo saltans | 33% | 100% |
A0A1X0P4T2 | Trypanosomatidae | 38% | 100% |
A0A3R7MCD3 | Trypanosoma rangeli | 39% | 100% |
A0A3S7XA27 | Leishmania donovani | 79% | 100% |
A4IC71 | Leishmania infantum | 79% | 100% |
C9ZYG3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AFX1 | Leishmania major | 79% | 100% |
E9B724 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
V5B4K6 | Trypanosoma cruzi | 39% | 100% |