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: A0A3Q8IGS5
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 | 218 | 220 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.345 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.352 |
DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.423 |
DOC_CYCLIN_RxL_1 | 39 | 47 | PF00134 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 294 | 300 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 5 | 11 | PF00134 | 0.194 |
DOC_MAPK_FxFP_2 | 13 | 16 | PF00069 | 0.194 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 333 | 341 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 206 | 214 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 334 | 343 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 175 | 181 | PF00149 | 0.528 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 294 | 297 | PF13499 | 0.486 |
DOC_PP2B_LxvP_1 | 36 | 39 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.194 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.194 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.414 |
DOC_USP7_UBL2_3 | 403 | 407 | PF12436 | 0.322 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.493 |
LIG_Actin_WH2_2 | 203 | 220 | PF00022 | 0.528 |
LIG_APCC_ABBA_1 | 376 | 381 | PF00400 | 0.433 |
LIG_APCC_ABBAyCdc20_2 | 139 | 145 | PF00400 | 0.423 |
LIG_APCC_ABBAyCdc20_2 | 369 | 375 | PF00400 | 0.293 |
LIG_BRCT_BRCA1_1 | 405 | 409 | PF00533 | 0.314 |
LIG_deltaCOP1_diTrp_1 | 285 | 293 | PF00928 | 0.480 |
LIG_EVH1_1 | 36 | 40 | PF00568 | 0.525 |
LIG_EVH1_2 | 10 | 14 | PF00568 | 0.194 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.590 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.480 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.528 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.693 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.421 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.528 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.500 |
LIG_GBD_Chelix_1 | 345 | 353 | PF00786 | 0.258 |
LIG_LIR_Apic_2 | 185 | 190 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 153 | 164 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 237 | 247 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 358 | 368 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 84 | 89 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 96 | 103 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 285 | 290 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.461 |
LIG_MAD2 | 42 | 50 | PF02301 | 0.446 |
LIG_MYND_1 | 34 | 38 | PF01753 | 0.534 |
LIG_NRBOX | 348 | 354 | PF00104 | 0.394 |
LIG_Pex14_2 | 13 | 17 | PF04695 | 0.194 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.468 |
LIG_SH3_2 | 37 | 42 | PF14604 | 0.580 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.499 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.453 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.486 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.531 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.528 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.675 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.220 |
LIG_SH3_CIN85_PxpxPR_1 | 134 | 139 | PF14604 | 0.423 |
LIG_SH3_CIN85_PxpxPR_1 | 37 | 42 | PF14604 | 0.496 |
LIG_SUMO_SIM_anti_2 | 166 | 174 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 166 | 174 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 350 | 356 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.486 |
LIG_SxIP_EBH_1 | 42 | 55 | PF03271 | 0.445 |
LIG_UBA3_1 | 426 | 434 | PF00899 | 0.366 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.465 |
LIG_WW_2 | 34 | 37 | PF00397 | 0.541 |
LIG_WW_3 | 39 | 43 | PF00397 | 0.599 |
MOD_CDK_SPK_2 | 134 | 139 | PF00069 | 0.433 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.554 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.528 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.388 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.456 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.507 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.317 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.222 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.236 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.297 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.468 |
MOD_GlcNHglycan | 389 | 393 | PF01048 | 0.673 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.595 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.442 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.593 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.393 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.493 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.248 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.334 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.566 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.416 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.578 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.343 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.494 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.469 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.363 |
MOD_PKA_1 | 333 | 339 | PF00069 | 0.407 |
MOD_PKA_1 | 403 | 409 | PF00069 | 0.404 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.552 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.456 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.277 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.399 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.505 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.490 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.497 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.481 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.453 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.419 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.444 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.594 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.482 |
TRG_DiLeu_BaEn_4 | 173 | 179 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P304 | Leptomonas seymouri | 56% | 100% |
A0A0N0P958 | Leptomonas seymouri | 26% | 100% |
A0A0S4JG88 | Bodo saltans | 32% | 100% |
A0A1X0P126 | Trypanosomatidae | 33% | 100% |
A0A3S7X466 | Leishmania donovani | 26% | 100% |
A4HJ26 | Leishmania braziliensis | 28% | 100% |
A4HLE0 | Leishmania braziliensis | 82% | 100% |
A4I6E8 | Leishmania infantum | 28% | 100% |
A4I8U9 | Leishmania infantum | 100% | 100% |
D0A4U6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E8NHM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B1J8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B3R8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q4A6 | Leishmania major | 93% | 100% |
Q4Q6L5 | Leishmania major | 25% | 92% |
V5BPD5 | Trypanosoma cruzi | 35% | 100% |