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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HQI5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.379 |
DOC_CDC14_PxL_1 | 14 | 22 | PF14671 | 0.569 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 191 | 198 | PF00069 | 0.686 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.689 |
DOC_MAPK_HePTP_8 | 72 | 84 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 341 | 348 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 75 | 84 | PF00069 | 0.731 |
DOC_MAPK_RevD_3 | 374 | 389 | PF00069 | 0.501 |
DOC_PP2B_LxvP_1 | 173 | 176 | PF13499 | 0.533 |
DOC_PP4_FxxP_1 | 142 | 145 | PF00568 | 0.497 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 341 | 345 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.673 |
LIG_Actin_WH2_2 | 283 | 298 | PF00022 | 0.556 |
LIG_Actin_WH2_2 | 58 | 76 | PF00022 | 0.440 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.501 |
LIG_BRCT_BRCA1_1 | 357 | 361 | PF00533 | 0.249 |
LIG_EH_1 | 180 | 184 | PF12763 | 0.712 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.385 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.459 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.469 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.697 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.728 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.726 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.716 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.297 |
LIG_NRBOX | 372 | 378 | PF00104 | 0.447 |
LIG_PDZ_Class_2 | 403 | 408 | PF00595 | 0.675 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.404 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.397 |
LIG_SH2_NCK_1 | 89 | 93 | PF00017 | 0.717 |
LIG_SH2_PTP2 | 162 | 165 | PF00017 | 0.249 |
LIG_SH2_PTP2 | 41 | 44 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.489 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.430 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.704 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.704 |
LIG_Sin3_3 | 36 | 43 | PF02671 | 0.229 |
LIG_SUMO_SIM_anti_2 | 112 | 117 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 345 | 350 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.249 |
LIG_TRFH_1 | 277 | 281 | PF08558 | 0.695 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.412 |
LIG_TYR_ITIM | 274 | 279 | PF00017 | 0.700 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.482 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.732 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.249 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.616 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.743 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.545 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.423 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.481 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.444 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.454 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.380 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.677 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.624 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.397 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.372 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.514 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.387 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.526 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.699 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.590 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.378 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.551 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.430 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.434 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.438 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.397 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.571 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.641 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.784 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.711 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.703 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.712 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.701 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I240 | Leptomonas seymouri | 48% | 100% |
A0A1X0NN35 | Trypanosomatidae | 22% | 100% |
A0A3S7XCE6 | Leishmania donovani | 74% | 100% |
E9AHZ4 | Leishmania infantum | 74% | 100% |
E9AU98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4Q093 | Leishmania major | 73% | 100% |