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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 5 |
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: E9B261
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 5 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 5 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 5 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 5 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 5 |
GO:0022857 | transmembrane transporter activity | 2 | 5 |
GO:1903425 | fluoride transmembrane transporter activity | 5 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.415 |
DEG_APCC_DBOX_1 | 222 | 230 | PF00400 | 0.297 |
DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.575 |
DEG_ODPH_VHL_1 | 139 | 152 | PF01847 | 0.377 |
DOC_CYCLIN_RxL_1 | 89 | 99 | PF00134 | 0.635 |
DOC_MAPK_MEF2A_6 | 147 | 154 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 96 | 105 | PF00069 | 0.503 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.374 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 127 | 137 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 147 | 153 | PF00244 | 0.447 |
LIG_14-3-3_CterR_2 | 252 | 255 | PF00244 | 0.646 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.414 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.336 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.447 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.641 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.367 |
LIG_GBD_Chelix_1 | 168 | 176 | PF00786 | 0.391 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 17 | 21 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.447 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.447 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.368 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.285 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.463 |
LIG_SH2_GRB2like | 120 | 123 | PF00017 | 0.373 |
LIG_SH2_GRB2like | 153 | 156 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 230 | 234 | PF00017 | 0.377 |
LIG_SH2_SRC | 228 | 231 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.301 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.263 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.447 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.574 |
LIG_SUMO_SIM_anti_2 | 4 | 9 | PF11976 | 0.615 |
LIG_TYR_ITIM | 16 | 21 | PF00017 | 0.563 |
LIG_Vh1_VBS_1 | 94 | 112 | PF01044 | 0.547 |
LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.285 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.405 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.244 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.319 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.422 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.660 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.505 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.470 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.338 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.244 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.225 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.330 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.334 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.662 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.534 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.173 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.363 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.285 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.297 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.356 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.568 |
MOD_OFUCOSY | 26 | 32 | PF10250 | 0.447 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.338 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.447 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.240 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.536 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.328 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.660 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P462 | Leptomonas seymouri | 58% | 91% |
A0A1X0NID7 | Trypanosomatidae | 34% | 76% |
A0A422NPK8 | Trypanosoma rangeli | 34% | 69% |
P0CU19 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 82% |
P0CU20 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 82% |