A small folded protein with a long C-terminal TM segment. Very unclear topology.. Expanded on multiple lineages, especially Strigomonas.
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: 5, no: 12 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q4A6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 1 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.344 |
CLV_PCSK_FUR_1 | 24 | 28 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.350 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.540 |
DOC_CYCLIN_RxL_1 | 56 | 64 | PF00134 | 0.309 |
DOC_CYCLIN_yCln2_LP_2 | 311 | 317 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 24 | 34 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 350 | 358 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 223 | 231 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 24 | 32 | PF00069 | 0.399 |
DOC_MAPK_MEF2A_6 | 351 | 360 | PF00069 | 0.470 |
DOC_MAPK_NFAT4_5 | 27 | 35 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 192 | 198 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.512 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.438 |
DOC_USP7_UBL2_3 | 420 | 424 | PF12436 | 0.348 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.541 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 50 | 60 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.516 |
LIG_Actin_WH2_2 | 220 | 237 | PF00022 | 0.550 |
LIG_Actin_WH2_2 | 261 | 276 | PF00022 | 0.399 |
LIG_Actin_WH2_2 | 35 | 52 | PF00022 | 0.434 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.539 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.457 |
LIG_APCC_ABBAyCdc20_2 | 156 | 162 | PF00400 | 0.440 |
LIG_APCC_ABBAyCdc20_2 | 386 | 392 | PF00400 | 0.409 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.271 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.340 |
LIG_deltaCOP1_diTrp_1 | 302 | 310 | PF00928 | 0.506 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.598 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.500 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.550 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.471 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.550 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.525 |
LIG_GBD_Chelix_1 | 362 | 370 | PF00786 | 0.281 |
LIG_LIR_Apic_2 | 202 | 207 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 101 | 106 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 111 | 120 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 254 | 264 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 101 | 105 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 309 | 313 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.358 |
LIG_NRBOX | 365 | 371 | PF00104 | 0.425 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.494 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.519 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.478 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.512 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.544 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.550 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.242 |
LIG_SH3_CIN85_PxpxPR_1 | 151 | 156 | PF14604 | 0.440 |
LIG_SUMO_SIM_anti_2 | 183 | 191 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 183 | 191 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 59 | 64 | PF11976 | 0.372 |
LIG_SxIP_EBH_1 | 59 | 72 | PF03271 | 0.312 |
LIG_UBA3_1 | 443 | 451 | PF00899 | 0.382 |
LIG_Vh1_VBS_1 | 2 | 20 | PF01044 | 0.537 |
LIG_WRC_WIRS_1 | 371 | 376 | PF05994 | 0.500 |
LIG_WW_3 | 56 | 60 | PF00397 | 0.412 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.454 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.547 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.522 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.413 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.482 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.535 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.332 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.345 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.240 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.306 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.412 |
MOD_GlcNHglycan | 406 | 410 | PF01048 | 0.697 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.622 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.578 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.607 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.566 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.506 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.268 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.355 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.581 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.422 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.441 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.589 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.353 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.363 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.495 |
MOD_PKA_1 | 420 | 426 | PF00069 | 0.428 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.540 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.550 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.610 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.557 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.427 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.528 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.533 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.501 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.462 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.373 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.363 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.446 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.425 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.468 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 372 | 381 | PF00179 | 0.566 |
TRG_DiLeu_BaEn_4 | 190 | 196 | PF01217 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.278 |
TRG_DiLeu_BaLyEn_6 | 91 | 96 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P304 | Leptomonas seymouri | 56% | 100% |
A0A0N0P958 | Leptomonas seymouri | 26% | 100% |
A0A0S4JG88 | Bodo saltans | 31% | 100% |
A0A1X0P126 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGS5 | Leishmania donovani | 93% | 100% |
A0A3S7X466 | Leishmania donovani | 26% | 100% |
A4HJ26 | Leishmania braziliensis | 26% | 100% |
A4HLE0 | Leishmania braziliensis | 80% | 100% |
A4I6E8 | Leishmania infantum | 26% | 100% |
A4I8U9 | Leishmania infantum | 93% | 100% |
D0A4U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E8NHM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B1J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B3R8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q6L5 | Leishmania major | 26% | 95% |
V5BPD5 | Trypanosoma cruzi | 35% | 100% |