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: E9B3R8
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 | 200 | 202 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.425 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.328 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.562 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.423 |
DOC_CYCLIN_RxL_1 | 21 | 29 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 276 | 282 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 315 | 323 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 157 | 163 | PF00149 | 0.528 |
DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.486 |
DOC_PP2B_LxvP_1 | 82 | 85 | PF13499 | 0.528 |
DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.375 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.246 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 385 | 389 | PF12436 | 0.324 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 9 | 19 | PF00244 | 0.638 |
LIG_Actin_WH2_2 | 185 | 202 | PF00022 | 0.528 |
LIG_AP2alpha_1 | 125 | 129 | PF02296 | 0.375 |
LIG_APCC_ABBA_1 | 358 | 363 | PF00400 | 0.429 |
LIG_APCC_ABBAyCdc20_2 | 121 | 127 | PF00400 | 0.423 |
LIG_APCC_ABBAyCdc20_2 | 351 | 357 | PF00400 | 0.289 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.246 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.316 |
LIG_deltaCOP1_diTrp_1 | 267 | 275 | PF00928 | 0.480 |
LIG_EVH1_1 | 19 | 23 | PF00568 | 0.541 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.476 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.528 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.740 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.416 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.594 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.528 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.500 |
LIG_LIR_Apic_2 | 127 | 132 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 167 | 172 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 274 | 282 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 322 | 333 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 66 | 71 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 322 | 328 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.461 |
LIG_MYND_1 | 17 | 21 | PF01753 | 0.558 |
LIG_NRBOX | 330 | 336 | PF00104 | 0.394 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.375 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.468 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.498 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.453 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.706 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.486 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.524 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.539 |
LIG_SH3_CIN85_PxpxPR_1 | 116 | 121 | PF14604 | 0.423 |
LIG_Sin3_3 | 325 | 332 | PF02671 | 0.253 |
LIG_SUMO_SIM_anti_2 | 148 | 156 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 148 | 156 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 24 | 29 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 332 | 338 | PF11976 | 0.447 |
LIG_SxIP_EBH_1 | 24 | 37 | PF03271 | 0.445 |
LIG_UBA3_1 | 408 | 416 | PF00899 | 0.365 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.375 |
LIG_WRC_WIRS_1 | 336 | 341 | PF05994 | 0.469 |
LIG_WW_3 | 21 | 25 | PF00397 | 0.625 |
MOD_CDK_SPK_2 | 116 | 121 | PF00069 | 0.433 |
MOD_CDK_SPxxK_3 | 35 | 42 | PF00069 | 0.554 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.548 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.504 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.388 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.457 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.469 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.504 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.412 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.339 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.313 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.271 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.462 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.223 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.281 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.196 |
MOD_GlcNHglycan | 370 | 375 | PF01048 | 0.673 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.342 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.420 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.591 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.521 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.485 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.530 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.568 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.244 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.334 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.566 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.416 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.487 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.510 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.334 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.472 |
MOD_PKA_1 | 315 | 321 | PF00069 | 0.396 |
MOD_PKA_1 | 385 | 391 | PF00069 | 0.408 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.541 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.485 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.400 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.508 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.475 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.439 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.480 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.440 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.477 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.417 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.622 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.489 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.534 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.490 |
TRG_DiLeu_BaEn_4 | 155 | 161 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P304 | Leptomonas seymouri | 57% | 96% |
A0A0N0P958 | Leptomonas seymouri | 26% | 100% |
A0A0S4JG88 | Bodo saltans | 32% | 100% |
A0A1X0P126 | Trypanosomatidae | 34% | 100% |
A0A3Q8IGS5 | Leishmania donovani | 93% | 96% |
A0A3S7X466 | Leishmania donovani | 26% | 100% |
A4HJ26 | Leishmania braziliensis | 26% | 100% |
A4HLE0 | Leishmania braziliensis | 82% | 100% |
A4I6E8 | Leishmania infantum | 26% | 100% |
A4I8U9 | Leishmania infantum | 93% | 96% |
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) | 26% | 100% |
Q4Q4A6 | Leishmania major | 90% | 100% |
Q4Q6L5 | Leishmania major | 27% | 100% |
V5BPD5 | Trypanosoma cruzi | 35% | 100% |