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: 4, no: 7 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HJ26
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 | 181 | 183 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.326 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.331 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.525 |
DOC_CYCLIN_RxL_1 | 8 | 16 | PF00134 | 0.327 |
DOC_MAPK_gen_1 | 131 | 140 | PF00069 | 0.219 |
DOC_MAPK_gen_1 | 236 | 245 | PF00069 | 0.217 |
DOC_MAPK_gen_1 | 375 | 382 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.217 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.281 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.327 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.308 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 126 | 132 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 354 | 358 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 39 | 43 | PF00244 | 0.318 |
LIG_Actin_WH2_2 | 24 | 41 | PF00022 | 0.288 |
LIG_APCC_ABBA_1 | 243 | 248 | PF00400 | 0.305 |
LIG_BIR_III_4 | 148 | 152 | PF00653 | 0.290 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.326 |
LIG_CaM_IQ_9 | 117 | 133 | PF13499 | 0.288 |
LIG_deltaCOP1_diTrp_1 | 266 | 274 | PF00928 | 0.331 |
LIG_DLG_GKlike_1 | 3 | 10 | PF00625 | 0.362 |
LIG_eIF4E_1 | 95 | 101 | PF01652 | 0.288 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.219 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.275 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.335 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.391 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.326 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.540 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.457 |
LIG_GBD_Chelix_1 | 316 | 324 | PF00786 | 0.362 |
LIG_IRF3_LxIS_1 | 117 | 123 | PF10401 | 0.326 |
LIG_LIR_Gen_1 | 133 | 144 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 72 | 80 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 94 | 101 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.502 |
LIG_MAD2 | 11 | 19 | PF02301 | 0.302 |
LIG_PCNA_yPIPBox_3 | 131 | 144 | PF02747 | 0.264 |
LIG_PDZ_Class_1 | 390 | 395 | PF00595 | 0.470 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.288 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.428 |
LIG_PTAP_UEV_1 | 279 | 284 | PF05743 | 0.219 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.288 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.288 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.303 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.293 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.190 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.343 |
LIG_SH3_1 | 277 | 283 | PF00018 | 0.288 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.326 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.314 |
LIG_SUMO_SIM_anti_2 | 96 | 105 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 96 | 105 | PF11976 | 0.329 |
LIG_WRC_WIRS_1 | 271 | 276 | PF05994 | 0.250 |
MOD_CDK_SPxxK_3 | 22 | 29 | PF00069 | 0.308 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.334 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.340 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.448 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.456 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.219 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.513 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.523 |
MOD_GlcNHglycan | 148 | 152 | PF01048 | 0.271 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.296 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.290 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.359 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.232 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.574 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.219 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.326 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.361 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.301 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.325 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.345 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.467 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.551 |
MOD_N-GLC_2 | 385 | 387 | PF02516 | 0.467 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.326 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.459 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.379 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.336 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.288 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.460 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.331 |
MOD_NEK2_2 | 246 | 251 | PF00069 | 0.326 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.299 |
MOD_PKA_1 | 125 | 131 | PF00069 | 0.299 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.299 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.348 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.262 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.469 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.416 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.542 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.288 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.340 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.386 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.250 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.501 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.266 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.308 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.308 |
MOD_SUMO_rev_2 | 55 | 63 | PF00179 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.269 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.303 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.322 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P958 | Leptomonas seymouri | 59% | 100% |
A0A3Q8IGS5 | Leishmania donovani | 28% | 91% |
A0A3S7X466 | Leishmania donovani | 80% | 100% |
A4I6E8 | Leishmania infantum | 80% | 100% |
A4I8U9 | Leishmania infantum | 28% | 91% |
E8NHM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9B1J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9B3R8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 95% |
Q4Q4A6 | Leishmania major | 26% | 100% |
Q4Q6L5 | Leishmania major | 78% | 100% |