A small and unique family of kinetoplastid proteins. No relationship to amastins.
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4QAU6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.685 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.377 |
CLV_PCSK_FUR_1 | 169 | 173 | PF00082 | 0.426 |
CLV_PCSK_FUR_1 | 174 | 178 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.376 |
CLV_PCSK_PC7_1 | 172 | 178 | PF00082 | 0.349 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.584 |
DOC_PP2B_PxIxI_1 | 107 | 113 | PF00149 | 0.323 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.527 |
DOC_PP4_MxPP_1 | 218 | 221 | PF00568 | 0.611 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.574 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 133 | 143 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.696 |
LIG_BIR_III_4 | 254 | 258 | PF00653 | 0.668 |
LIG_deltaCOP1_diTrp_1 | 120 | 130 | PF00928 | 0.309 |
LIG_deltaCOP1_diTrp_1 | 168 | 175 | PF00928 | 0.624 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.701 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.498 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.552 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.716 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 229 | 238 | PF02991 | 0.686 |
LIG_LIR_Gen_1 | 34 | 44 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 48 | 56 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.214 |
LIG_Pex14_1 | 101 | 105 | PF04695 | 0.593 |
LIG_Pex14_1 | 20 | 24 | PF04695 | 0.621 |
LIG_Pex14_2 | 161 | 165 | PF04695 | 0.387 |
LIG_PTB_Apo_2 | 72 | 79 | PF02174 | 0.285 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.650 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.696 |
LIG_SH2_NCK_1 | 232 | 236 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.640 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.491 |
LIG_SUMO_SIM_par_1 | 108 | 114 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 209 | 214 | PF11976 | 0.686 |
LIG_SUMO_SIM_par_1 | 80 | 86 | PF11976 | 0.323 |
LIG_TYR_ITIM | 151 | 156 | PF00017 | 0.385 |
LIG_TYR_ITIM | 230 | 235 | PF00017 | 0.637 |
LIG_ULM_U2AF65_1 | 171 | 176 | PF00076 | 0.452 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.333 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.468 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.224 |
MOD_Cter_Amidation | 245 | 248 | PF01082 | 0.601 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.499 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.367 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.476 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.444 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.623 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.434 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.717 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.348 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.495 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.320 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.301 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.323 |
MOD_NEK2_2 | 31 | 36 | PF00069 | 0.401 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.434 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.512 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.588 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.650 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.669 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.470 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.661 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.455 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.673 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.420 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.319 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.361 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.641 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.323 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.673 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZY6 | Leptomonas seymouri | 57% | 100% |
A0A1X0NJ34 | Trypanosomatidae | 33% | 72% |
A0A3S5ISN9 | Trypanosoma rangeli | 28% | 91% |
A0A3S7WY31 | Leishmania donovani | 93% | 100% |
A4HD91 | Leishmania braziliensis | 73% | 91% |
D0A705 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AH46 | Leishmania infantum | 93% | 100% |
E9AWM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |