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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q4L3
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0006829 | zinc ion transport | 8 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0030001 | metal ion transport | 6 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071577 | zinc ion transmembrane transport | 6 | 2 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 2 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 2 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 3 |
GO:0005385 | zinc ion transmembrane transporter activity | 7 | 2 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 3 |
GO:0046915 | transition metal ion transmembrane transporter activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 30 | 34 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 28 | 34 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.419 |
DEG_SPOP_SBC_1 | 270 | 274 | PF00917 | 0.457 |
DOC_CKS1_1 | 228 | 233 | PF01111 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.480 |
DOC_MAPK_MEF2A_6 | 171 | 180 | PF00069 | 0.528 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.305 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.436 |
LIG_14-3-3_CanoR_1 | 32 | 40 | PF00244 | 0.645 |
LIG_Actin_WH2_2 | 288 | 306 | PF00022 | 0.368 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.610 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.639 |
LIG_BRCT_BRCA1_1 | 252 | 256 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.355 |
LIG_Clathr_ClatBox_1 | 150 | 154 | PF01394 | 0.584 |
LIG_CSL_BTD_1 | 6 | 9 | PF09270 | 0.597 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.743 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.620 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.567 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.479 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.699 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.521 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.355 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.656 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.364 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 233 | 243 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 287 | 298 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.562 |
LIG_NRBOX | 134 | 140 | PF00104 | 0.558 |
LIG_Pex14_1 | 7 | 11 | PF04695 | 0.633 |
LIG_Rb_LxCxE_1 | 296 | 314 | PF01857 | 0.285 |
LIG_REV1ctd_RIR_1 | 9 | 19 | PF16727 | 0.619 |
LIG_SH2_PTP2 | 292 | 295 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.523 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.574 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 131 | 139 | PF11976 | 0.597 |
LIG_SUMO_SIM_anti_2 | 271 | 280 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 60 | 65 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 112 | 119 | PF11976 | 0.771 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.659 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.480 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.393 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.486 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.668 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.513 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.587 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.416 |
MOD_GlcNHglycan | 154 | 158 | PF01048 | 0.402 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.396 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.365 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.710 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.379 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.334 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.661 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.715 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.789 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.617 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.480 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.504 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.419 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.324 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.610 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.463 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.595 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.580 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.423 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.524 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.592 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.268 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.678 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.668 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.659 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.672 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.675 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.556 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.461 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.423 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.321 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.212 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.389 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.610 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.677 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U6 | Leptomonas seymouri | 49% | 95% |
A0A1X0P3V2 | Trypanosomatidae | 30% | 75% |
A0A3R7MSD3 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X6D4 | Leishmania donovani | 88% | 100% |
A4HL46 | Leishmania braziliensis | 68% | 100% |
A4I8M5 | Leishmania infantum | 88% | 100% |
C9ZPV0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
E9B3I7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BAE0 | Trypanosoma cruzi | 38% | 92% |