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: Q4QEJ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.281 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.242 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.418 |
DOC_CYCLIN_RxL_1 | 205 | 216 | PF00134 | 0.539 |
DOC_MAPK_DCC_7 | 120 | 128 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 205 | 212 | PF00069 | 0.648 |
DOC_MAPK_MEF2A_6 | 120 | 128 | PF00069 | 0.355 |
DOC_MAPK_RevD_3 | 128 | 143 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 31 | 38 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.675 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.309 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.630 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.232 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.448 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.315 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.474 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.230 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 7 | 18 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.203 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.258 |
LIG_PCNA_PIPBox_1 | 23 | 32 | PF02747 | 0.465 |
LIG_PDZ_Class_2 | 220 | 225 | PF00595 | 0.616 |
LIG_Pex14_1 | 117 | 121 | PF04695 | 0.249 |
LIG_Rb_LxCxE_1 | 84 | 98 | PF01857 | 0.335 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.273 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.282 |
LIG_SH2_PTP2 | 102 | 105 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.294 |
LIG_SUMO_SIM_anti_2 | 216 | 223 | PF11976 | 0.598 |
LIG_SUMO_SIM_anti_2 | 47 | 52 | PF11976 | 0.183 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.307 |
LIG_TRFH_1 | 197 | 201 | PF08558 | 0.280 |
LIG_TYR_ITIM | 100 | 105 | PF00017 | 0.307 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.161 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.435 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.319 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.431 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.349 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.173 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.353 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.287 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.171 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.676 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.372 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.642 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.665 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.325 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.236 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.312 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.279 |
MOD_SUMO_rev_2 | 6 | 11 | PF00179 | 0.283 |
TRG_DiLeu_BaEn_1 | 92 | 97 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_2 | 58 | 64 | PF01217 | 0.218 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.181 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.233 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.481 |
TRG_NES_CRM1_1 | 98 | 113 | PF08389 | 0.420 |
TRG_NLS_MonoExtN_4 | 205 | 210 | PF00514 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 33 | 38 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1L8 | Leptomonas seymouri | 59% | 100% |
A0A0N1IHQ2 | Leptomonas seymouri | 36% | 100% |
A0A0S4J3W8 | Bodo saltans | 36% | 100% |
A0A0S4J4A1 | Bodo saltans | 36% | 100% |
A0A1X0NUH8 | Trypanosomatidae | 41% | 100% |
A0A1X0NUR6 | Trypanosomatidae | 35% | 100% |
A0A3Q8ICP7 | Leishmania donovani | 34% | 100% |
A0A3R7NKX5 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H6Z5 | Leishmania donovani | 96% | 100% |
A4H8U8 | Leishmania braziliensis | 34% | 100% |
A4HX66 | Leishmania infantum | 34% | 100% |
A4HX67 | Leishmania infantum | 96% | 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) | 28% | 100% |
E9ARC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ARC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QEJ7 | Leishmania major | 34% | 100% |
V5ASR1 | Trypanosoma cruzi | 33% | 100% |
V5BCQ2 | Trypanosoma cruzi | 40% | 100% |