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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HHH8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0005215 | transporter activity | 1 | 1 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 1 |
GO:0022804 | active transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.351 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.459 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.258 |
DEG_COP1_1 | 411 | 420 | PF00400 | 0.466 |
DOC_CYCLIN_RxL_1 | 162 | 173 | PF00134 | 0.241 |
DOC_CYCLIN_RxL_1 | 202 | 210 | PF00134 | 0.328 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.472 |
DOC_MAPK_gen_1 | 110 | 117 | PF00069 | 0.268 |
DOC_MAPK_gen_1 | 202 | 211 | PF00069 | 0.264 |
DOC_MAPK_gen_1 | 272 | 281 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 99 | 106 | PF00069 | 0.410 |
DOC_MAPK_NFAT4_5 | 99 | 107 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 163 | 170 | PF00149 | 0.281 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.532 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.477 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.624 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.169 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 163 | 168 | PF00244 | 0.252 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 27 | 34 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 272 | 281 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 389 | 395 | PF00244 | 0.460 |
LIG_APCC_ABBA_1 | 424 | 429 | PF00400 | 0.479 |
LIG_BIR_III_2 | 31 | 35 | PF00653 | 0.431 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.214 |
LIG_Clathr_ClatBox_1 | 245 | 249 | PF01394 | 0.180 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.237 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.281 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.237 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.383 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.362 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.353 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.433 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.638 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.237 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.466 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.443 |
LIG_Integrin_isoDGR_2 | 146 | 148 | PF01839 | 0.261 |
LIG_LIR_Gen_1 | 113 | 120 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 173 | 182 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 360 | 369 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.527 |
LIG_SH2_GRB2like | 363 | 366 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 290 | 294 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.320 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.405 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.477 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.281 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.594 |
LIG_SUMO_SIM_anti_2 | 244 | 250 | PF11976 | 0.268 |
LIG_SUMO_SIM_anti_2 | 260 | 265 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.237 |
LIG_SUMO_SIM_par_1 | 256 | 265 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 63 | 73 | PF11976 | 0.465 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.482 |
LIG_UBA3_1 | 192 | 199 | PF00899 | 0.268 |
LIG_UBA3_1 | 266 | 275 | PF00899 | 0.343 |
LIG_WRC_WIRS_1 | 171 | 176 | PF05994 | 0.281 |
MOD_CDK_SPK_2 | 194 | 199 | PF00069 | 0.169 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.210 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.281 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.513 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.545 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.532 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.357 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.521 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.238 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.304 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.427 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.660 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.540 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.511 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.569 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.285 |
MOD_GlcNHglycan | 224 | 228 | PF01048 | 0.291 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.467 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.600 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.433 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.251 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.488 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.541 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.668 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.548 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.223 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.459 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.476 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.429 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.237 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.338 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.490 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.616 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.449 |
MOD_PK_1 | 90 | 96 | PF00069 | 0.423 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.295 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.314 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.539 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.434 |
MOD_Plk_2-3 | 339 | 345 | PF00069 | 0.435 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.298 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.273 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.340 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.268 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.399 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.169 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.495 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.557 |
TRG_DiLeu_BaEn_1 | 262 | 267 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.268 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.237 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.237 |
TRG_ER_KDEL_1 | 434 | 437 | PF00810 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ICD4 | Leptomonas seymouri | 59% | 93% |
A0A0S4J9X9 | Bodo saltans | 57% | 100% |
A0A3S7X2I8 | Leishmania donovani | 68% | 94% |
A4H4H6 | Leishmania braziliensis | 30% | 66% |
A4I4M8 | Leishmania infantum | 68% | 94% |
E9AE26 | Leishmania major | 68% | 100% |
E9ALQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 94% |
E9ANF0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
Q134N9 | Rhodopseudomonas palustris (strain BisB5) | 34% | 100% |
Q21BU8 | Rhodopseudomonas palustris (strain BisB18) | 31% | 100% |
Q6N9W0 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 31% | 100% |
Q8G5P8 | Bifidobacterium longum (strain NCC 2705) | 30% | 100% |
V5D9U5 | Trypanosoma cruzi | 63% | 100% |