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 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X2I8
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 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
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 | 24 | 28 | PF00656 | 0.597 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.292 |
DOC_CYCLIN_RxL_1 | 178 | 189 | PF00134 | 0.266 |
DOC_CYCLIN_RxL_1 | 218 | 226 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 413 | 419 | PF00134 | 0.603 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 218 | 227 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.292 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.716 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.710 |
DOC_USP7_UBL2_3 | 211 | 215 | PF12436 | 0.296 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.525 |
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 | 0.378 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.769 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.583 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.683 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.292 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.297 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.328 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.382 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.361 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.361 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.520 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.292 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.648 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.462 |
LIG_Integrin_isoDGR_2 | 162 | 164 | PF01839 | 0.335 |
LIG_LIR_Apic_2 | 20 | 26 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 129 | 136 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 347 | 355 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.559 |
LIG_LYPXL_yS_3 | 75 | 78 | PF13949 | 0.355 |
LIG_PTB_Apo_2 | 179 | 186 | PF02174 | 0.313 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.439 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.432 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.497 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.292 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.585 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.534 |
LIG_SUMO_SIM_anti_2 | 260 | 266 | PF11976 | 0.292 |
LIG_SUMO_SIM_anti_2 | 276 | 281 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 260 | 266 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 80 | 89 | PF11976 | 0.468 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.620 |
LIG_UBA3_1 | 208 | 215 | PF00899 | 0.351 |
LIG_UBA3_1 | 282 | 291 | PF00899 | 0.427 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.292 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.336 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.472 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.686 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.292 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.548 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.783 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.573 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.545 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.600 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.342 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.295 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.331 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.633 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.556 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.460 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.443 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.292 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.605 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.291 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.292 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.792 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.599 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.503 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.561 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.641 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.518 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.604 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.292 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.621 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.746 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.543 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.574 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.603 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.490 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.590 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.292 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.597 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.658 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.630 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.292 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.375 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.642 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.400 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.534 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.650 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.451 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.292 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.404 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.351 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.351 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.339 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.600 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.563 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.621 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.527 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.746 |
MOD_SUMO_rev_2 | 167 | 173 | PF00179 | 0.337 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.292 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.292 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ICD4 | Leptomonas seymouri | 76% | 99% |
A0A0S4J9X9 | Bodo saltans | 58% | 100% |
A4HHH8 | Leishmania braziliensis | 68% | 96% |
A4I4M8 | Leishmania infantum | 99% | 100% |
E9AE26 | Leishmania major | 89% | 100% |
E9ALQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |