Consists of a conserved FAD-binding domain. No TM segments are present.
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4Q5U2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.505 |
CLV_MEL_PAP_1 | 329 | 335 | PF00089 | 0.290 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.238 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.303 |
CLV_PCSK_PC7_1 | 88 | 94 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.317 |
DOC_MAPK_gen_1 | 159 | 168 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 69 | 77 | PF00069 | 0.485 |
DOC_MAPK_HePTP_8 | 219 | 231 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 222 | 231 | PF00069 | 0.577 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.232 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.468 |
DOC_SPAK_OSR1_1 | 330 | 334 | PF12202 | 0.488 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.407 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 159 | 168 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 19 | 27 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 281 | 289 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 93 | 103 | PF00244 | 0.510 |
LIG_Actin_WH2_2 | 154 | 169 | PF00022 | 0.488 |
LIG_Actin_WH2_2 | 286 | 303 | PF00022 | 0.543 |
LIG_AP2alpha_2 | 344 | 346 | PF02296 | 0.463 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.614 |
LIG_Clathr_ClatBox_1 | 230 | 234 | PF01394 | 0.556 |
LIG_Clathr_ClatBox_1 | 340 | 344 | PF01394 | 0.460 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.521 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.449 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.563 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.530 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.516 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.476 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.487 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.586 |
LIG_Integrin_RGD_1 | 349 | 351 | PF01839 | 0.270 |
LIG_Integrin_RGD_1 | 374 | 376 | PF01839 | 0.420 |
LIG_LIR_Gen_1 | 163 | 172 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 213 | 221 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.492 |
LIG_MYND_1 | 129 | 133 | PF01753 | 0.480 |
LIG_Rb_LxCxE_1 | 105 | 116 | PF01857 | 0.523 |
LIG_Rb_pABgroove_1 | 225 | 233 | PF01858 | 0.513 |
LIG_SH2_NCK_1 | 86 | 90 | PF00017 | 0.546 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.521 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.462 |
LIG_SUMO_SIM_anti_2 | 225 | 232 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 253 | 259 | PF11976 | 0.468 |
LIG_SUMO_SIM_anti_2 | 38 | 44 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 72 | 79 | PF11976 | 0.545 |
LIG_SUMO_SIM_par_1 | 20 | 28 | PF11976 | 0.489 |
LIG_UBA3_1 | 103 | 112 | PF00899 | 0.483 |
LIG_UBA3_1 | 206 | 211 | PF00899 | 0.533 |
MOD_CDK_SPxxK_3 | 318 | 325 | PF00069 | 0.511 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.517 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.452 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.562 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.186 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.548 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.493 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.545 |
MOD_Cter_Amidation | 368 | 371 | PF01082 | 0.337 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.346 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.328 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.352 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.338 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.343 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.232 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.417 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.544 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.609 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.531 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.578 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.495 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.614 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.377 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.507 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.679 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.270 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.625 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.213 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.616 |
MOD_PK_1 | 113 | 119 | PF00069 | 0.538 |
MOD_PK_1 | 243 | 249 | PF00069 | 0.534 |
MOD_PK_1 | 310 | 316 | PF00069 | 0.564 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.616 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.564 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.550 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.490 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.572 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.515 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.608 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.440 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.543 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.515 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.538 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.760 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.600 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.571 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.498 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.607 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.521 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.577 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.540 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.539 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.513 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.558 |
MOD_SUMO_for_1 | 324 | 327 | PF00179 | 0.547 |
MOD_SUMO_rev_2 | 106 | 115 | PF00179 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.579 |
TRG_DiLeu_BaLyEn_6 | 408 | 413 | PF01217 | 0.634 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 125 | 130 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 159 | 164 | PF00026 | 0.269 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.338 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ2 | Leptomonas seymouri | 71% | 100% |
A0A0S4IXP3 | Bodo saltans | 46% | 100% |
A0A1X0NIV3 | Trypanosomatidae | 55% | 100% |
A0A3S7X516 | Leishmania donovani | 96% | 100% |
A4HJV9 | Leishmania braziliensis | 88% | 100% |
A4I7C1 | Leishmania infantum | 96% | 100% |
C9ZMI3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
C9ZWI4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9B2B4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5B4U1 | Trypanosoma cruzi | 55% | 100% |