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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 8 |
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: Q4Q5Z9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006820 | monoatomic anion transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015698 | inorganic anion 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:0098656 | monoatomic anion transmembrane transport | 4 | 2 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 2 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 2 |
GO:1903424 | fluoride transmembrane transport | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 8 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 8 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 8 |
GO:0015103 | inorganic anion transmembrane transporter activity | 4 | 8 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 8 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
GO:1903425 | fluoride transmembrane transporter activity | 5 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.677 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.351 |
DEG_APCC_DBOX_1 | 228 | 236 | PF00400 | 0.598 |
DEG_APCC_DBOX_1 | 9 | 17 | PF00400 | 0.635 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.732 |
DEG_ODPH_VHL_1 | 276 | 289 | PF01847 | 0.432 |
DOC_AGCK_PIF_1 | 122 | 127 | PF00069 | 0.240 |
DOC_CYCLIN_RxL_1 | 226 | 236 | PF00134 | 0.576 |
DOC_MAPK_MEF2A_6 | 284 | 291 | PF00069 | 0.417 |
DOC_PP1_RVXF_1 | 206 | 213 | PF00149 | 0.605 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.766 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.343 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 264 | 274 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 284 | 290 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 360 | 369 | PF00244 | 0.258 |
LIG_14-3-3_CterR_2 | 388 | 392 | PF00244 | 0.660 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.413 |
LIG_Clathr_ClatBox_2 | 220 | 225 | PF01394 | 0.624 |
LIG_deltaCOP1_diTrp_1 | 219 | 225 | PF00928 | 0.574 |
LIG_EH_1 | 118 | 122 | PF12763 | 0.307 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.414 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.674 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.361 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.408 |
LIG_GBD_Chelix_1 | 305 | 313 | PF00786 | 0.435 |
LIG_LIR_Apic_2 | 126 | 130 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 371 | 381 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.672 |
LIG_NRBOX | 309 | 315 | PF00104 | 0.413 |
LIG_Pex14_2 | 136 | 140 | PF04695 | 0.365 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.409 |
LIG_Pex14_2 | 240 | 244 | PF04695 | 0.334 |
LIG_PTB_Apo_2 | 116 | 123 | PF02174 | 0.336 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.390 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.365 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.540 |
LIG_SH2_GRB2like | 290 | 293 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 367 | 371 | PF00017 | 0.417 |
LIG_SH2_PTP2 | 127 | 130 | PF00017 | 0.402 |
LIG_SH2_SRC | 365 | 368 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.570 |
LIG_SH2_STAT3 | 65 | 68 | PF00017 | 0.821 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.655 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.340 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.456 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.651 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.337 |
LIG_SH3_3 | 378 | 384 | PF00018 | 0.413 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.782 |
LIG_SUMO_SIM_anti_2 | 141 | 146 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 89 | 94 | PF11976 | 0.421 |
LIG_Vh1_VBS_1 | 231 | 249 | PF01044 | 0.540 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.402 |
LIG_WRC_WIRS_1 | 166 | 171 | PF05994 | 0.351 |
LIG_WRC_WIRS_1 | 352 | 357 | PF05994 | 0.340 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.308 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.363 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.284 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.795 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.569 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.655 |
MOD_CMANNOS | 222 | 225 | PF00535 | 0.434 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.413 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.513 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.351 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.565 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.535 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.384 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.632 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.284 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.394 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.263 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.624 |
MOD_N-GLC_2 | 2 | 4 | PF02516 | 0.525 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.344 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.373 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.351 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.570 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.212 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.419 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.334 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.409 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.772 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.818 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.721 |
MOD_PKB_1 | 10 | 18 | PF00069 | 0.638 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.323 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.381 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.369 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.373 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.621 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.359 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.418 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.370 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.793 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.678 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.768 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.738 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.655 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.585 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.634 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P462 | Leptomonas seymouri | 61% | 100% |
A0A1X0NID7 | Trypanosomatidae | 35% | 100% |
A0A3Q8IGC8 | Leishmania donovani | 89% | 100% |
A0A422NPK8 | Trypanosoma rangeli | 35% | 100% |
A4HJQ0 | Leishmania braziliensis | 73% | 100% |
A4I767 | Leishmania infantum | 89% | 100% |