Very distantly similar to animal TMEM8 and MMD2 proteins. Its function is obscure, although gene fusions with lipid hydrolases suggest a related function
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: 1, no: 20 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 22 |
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: A0A3S5H6Z5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.303 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.266 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.444 |
DOC_CYCLIN_RxL_1 | 205 | 216 | PF00134 | 0.682 |
DOC_MAPK_DCC_7 | 120 | 128 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 205 | 212 | PF00069 | 0.659 |
DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.365 |
DOC_MAPK_RevD_3 | 128 | 143 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 31 | 38 | PF00149 | 0.444 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.694 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.558 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.342 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.625 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.262 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.465 |
LIG_BIR_III_4 | 217 | 221 | PF00653 | 0.505 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.347 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.486 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 7 | 18 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.142 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.305 |
LIG_PCNA_PIPBox_1 | 23 | 32 | PF02747 | 0.473 |
LIG_PDZ_Class_2 | 220 | 225 | PF00595 | 0.575 |
LIG_Pex14_1 | 117 | 121 | PF04695 | 0.266 |
LIG_Rb_LxCxE_1 | 84 | 98 | PF01857 | 0.367 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.305 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.322 |
LIG_SH2_PTP2 | 102 | 105 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.299 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.340 |
LIG_TRFH_1 | 197 | 201 | PF08558 | 0.322 |
LIG_TYR_ITIM | 100 | 105 | PF00017 | 0.344 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.169 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.437 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.330 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.444 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.339 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.380 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.371 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.290 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.673 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.364 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.648 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.667 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.311 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.258 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.318 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.261 |
MOD_SUMO_rev_2 | 6 | 11 | PF00179 | 0.315 |
TRG_DiLeu_BaEn_1 | 92 | 97 | PF01217 | 0.547 |
TRG_DiLeu_BaEn_2 | 58 | 64 | PF01217 | 0.244 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.196 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.259 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.504 |
TRG_NES_CRM1_1 | 98 | 113 | PF08389 | 0.439 |
TRG_NLS_MonoExtN_4 | 205 | 210 | PF00514 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 33 | 38 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1L8 | Leptomonas seymouri | 60% | 100% |
A0A0N1IHQ2 | Leptomonas seymouri | 37% | 100% |
A0A0S4J3W8 | Bodo saltans | 37% | 100% |
A0A0S4J4A1 | Bodo saltans | 36% | 100% |
A0A1X0NUH8 | Trypanosomatidae | 42% | 100% |
A0A1X0NUR6 | Trypanosomatidae | 34% | 100% |
A0A3Q8ICP7 | Leishmania donovani | 33% | 100% |
A0A3R7NKX5 | Trypanosoma rangeli | 32% | 100% |
A4H8U8 | Leishmania braziliensis | 35% | 100% |
A4HX66 | Leishmania infantum | 33% | 100% |
A4HX67 | Leishmania infantum | 100% | 100% |
C9ZTT2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZTT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ARC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9ARC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QEJ6 | Leishmania major | 96% | 100% |
Q4QEJ7 | Leishmania major | 33% | 100% |
V5ASR1 | Trypanosoma cruzi | 33% | 100% |
V5BCQ2 | Trypanosoma cruzi | 40% | 100% |