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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AE26
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005215 | transporter activity | 1 | 2 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0022804 | active transmembrane transporter activity | 3 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 2 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.466 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.422 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.329 |
DOC_CYCLIN_RxL_1 | 218 | 226 | PF00134 | 0.410 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.540 |
DOC_CYCLIN_yCln2_LP_2 | 414 | 420 | PF00134 | 0.605 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 218 | 227 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.385 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.329 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.597 |
DOC_PP2B_LxvP_1 | 414 | 417 | PF13499 | 0.600 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.719 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.746 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 288 | 297 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.759 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.604 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.590 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.691 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.329 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.329 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.420 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.426 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.315 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.536 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.536 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.329 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.687 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.561 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.531 |
LIG_Integrin_isoDGR_2 | 162 | 164 | PF01839 | 0.349 |
LIG_LIR_Apic_2 | 20 | 26 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 129 | 136 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.636 |
LIG_PTB_Apo_2 | 179 | 186 | PF02174 | 0.324 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.460 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.482 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.545 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.353 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 260 | 266 | PF11976 | 0.324 |
LIG_SUMO_SIM_anti_2 | 276 | 281 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 260 | 266 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 80 | 89 | PF11976 | 0.512 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.636 |
LIG_UBA3_1 | 208 | 215 | PF00899 | 0.418 |
LIG_UBA3_1 | 282 | 291 | PF00899 | 0.462 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.329 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.370 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.494 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.693 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.329 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.580 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.630 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.604 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.617 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.625 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.548 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.376 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.329 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.294 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.650 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.458 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.516 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.307 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.632 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.336 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.737 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.655 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.734 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.605 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.701 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.613 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.299 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.340 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.690 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.551 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.744 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.569 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.403 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.616 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.410 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.716 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.655 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.705 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.333 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.284 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.557 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.402 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.637 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.306 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.393 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.599 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.730 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.428 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.682 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.482 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.318 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.413 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.388 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.388 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.294 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.645 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.526 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.669 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.583 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.641 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.576 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.682 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.763 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.747 |
MOD_SUMO_rev_2 | 167 | 173 | PF00179 | 0.374 |
MOD_SUMO_rev_2 | 89 | 98 | PF00179 | 0.388 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.447 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8R4 | Leptomonas seymouri | 23% | 89% |
A0A0N1ICD4 | Leptomonas seymouri | 73% | 99% |
A0A0S4J9X9 | Bodo saltans | 57% | 100% |
A0A3S7X2I8 | Leishmania donovani | 89% | 100% |
A4HHH8 | Leishmania braziliensis | 68% | 100% |
A4I4M8 | Leishmania infantum | 89% | 100% |
E9ALQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |