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 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALQ7
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 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
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: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:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
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 | 0.665 |
CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.485 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.491 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.498 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.346 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.500 |
DOC_CYCLIN_RxL_1 | 178 | 189 | PF00134 | 0.316 |
DOC_CYCLIN_RxL_1 | 218 | 226 | PF00134 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 118 | 124 | PF00134 | 0.565 |
DOC_CYCLIN_yCln2_LP_2 | 413 | 419 | PF00134 | 0.638 |
DOC_MAPK_gen_1 | 126 | 133 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 218 | 227 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.406 |
DOC_PP1_RVXF_1 | 179 | 186 | PF00149 | 0.346 |
DOC_PP2B_LxvP_1 | 118 | 121 | PF13499 | 0.622 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.634 |
DOC_PP4_MxPP_1 | 399 | 402 | PF00568 | 0.501 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.686 |
DOC_USP7_UBL2_3 | 211 | 215 | PF12436 | 0.340 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 288 | 297 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.769 |
LIG_APCC_ABBAyCdc20_2 | 41 | 47 | PF00400 | 0.493 |
LIG_Clathr_ClatBox_1 | 261 | 265 | PF01394 | 0.260 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.346 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.346 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.346 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.445 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.419 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.416 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.613 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.488 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.513 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.333 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.489 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.722 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.498 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.559 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.513 |
LIG_LIR_Gen_1 | 129 | 136 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 189 | 198 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 129 | 133 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.446 |
LIG_PTB_Apo_2 | 179 | 186 | PF02174 | 0.360 |
LIG_SH2_STAP1 | 306 | 310 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 335 | 339 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.440 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.504 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.569 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.319 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.563 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.491 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 260 | 266 | PF11976 | 0.350 |
LIG_SUMO_SIM_anti_2 | 276 | 281 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 19 | 27 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 260 | 266 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 80 | 89 | PF11976 | 0.471 |
LIG_TRAF2_1 | 103 | 106 | PF00917 | 0.554 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.695 |
LIG_UBA3_1 | 208 | 215 | PF00899 | 0.403 |
LIG_UBA3_1 | 282 | 291 | PF00899 | 0.481 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.346 |
MOD_CDC14_SPxK_1 | 123 | 126 | PF00782 | 0.268 |
MOD_CDK_SPxK_1 | 120 | 126 | PF00069 | 0.304 |
MOD_CDK_SPxxK_3 | 120 | 127 | PF00069 | 0.306 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.355 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.512 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.346 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.702 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.617 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.646 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.555 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.652 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.631 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.490 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.392 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.346 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.311 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.712 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.567 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.486 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.495 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.326 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.660 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.340 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.342 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.598 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.624 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.723 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.354 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.646 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.725 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.607 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.671 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.665 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.547 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.337 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.629 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.567 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.702 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.585 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.643 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.346 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.431 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.765 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.613 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.714 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.490 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.311 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.391 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.403 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.403 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.362 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.557 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.436 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.668 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.612 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.502 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.750 |
MOD_SUMO_for_1 | 330 | 333 | PF00179 | 0.289 |
MOD_SUMO_rev_2 | 167 | 173 | PF00179 | 0.391 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.465 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.329 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ICD4 | Leptomonas seymouri | 74% | 99% |
A0A0S4J9X9 | Bodo saltans | 58% | 100% |
A0A3S7X2I8 | Leishmania donovani | 86% | 100% |
A4HHH8 | Leishmania braziliensis | 70% | 96% |
A4I4M8 | Leishmania infantum | 85% | 100% |
C9ZQV0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 89% |
E9AE26 | Leishmania major | 83% | 100% |