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: 5 |
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 | yes | yes: 3, no: 2 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HVZ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 119 | 123 | PF00656 | 0.411 |
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.415 |
CLV_MEL_PAP_1 | 156 | 162 | PF00089 | 0.576 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.603 |
DEG_SPOP_SBC_1 | 259 | 263 | PF00917 | 0.386 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.460 |
DOC_CYCLIN_RxL_1 | 201 | 212 | PF00134 | 0.419 |
DOC_CYCLIN_RxL_1 | 304 | 318 | PF00134 | 0.599 |
DOC_MAPK_gen_1 | 308 | 317 | PF00069 | 0.596 |
DOC_MAPK_HePTP_8 | 307 | 319 | PF00069 | 0.571 |
DOC_MAPK_HePTP_8 | 9 | 21 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 12 | 21 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 310 | 319 | PF00069 | 0.593 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.443 |
DOC_PP2B_PxIxI_1 | 304 | 310 | PF00149 | 0.583 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 209 | 214 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 243 | 252 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 324 | 332 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.375 |
LIG_Actin_WH2_2 | 153 | 168 | PF00022 | 0.402 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.509 |
LIG_BIR_III_4 | 219 | 223 | PF00653 | 0.475 |
LIG_Clathr_ClatBox_1 | 314 | 318 | PF01394 | 0.589 |
LIG_deltaCOP1_diTrp_1 | 223 | 226 | PF00928 | 0.373 |
LIG_DLG_GKlike_1 | 209 | 216 | PF00625 | 0.370 |
LIG_FAT_LD_1 | 282 | 290 | PF03623 | 0.305 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.464 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.374 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.335 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.595 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.447 |
LIG_GBD_Chelix_1 | 95 | 103 | PF00786 | 0.580 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.352 |
LIG_LYPXL_yS_3 | 83 | 86 | PF13949 | 0.369 |
LIG_NRBOX | 16 | 22 | PF00104 | 0.573 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.422 |
LIG_Pex14_2 | 188 | 192 | PF04695 | 0.486 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.277 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.491 |
LIG_SH2_SRC | 196 | 199 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.356 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.480 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.305 |
LIG_Sin3_3 | 16 | 23 | PF02671 | 0.482 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 283 | 289 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 316 | 321 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 313 | 318 | PF11976 | 0.589 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.630 |
LIG_TYR_ITSM | 79 | 86 | PF00017 | 0.391 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.458 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.479 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.554 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.808 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.463 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.452 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.642 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.591 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.618 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.633 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.459 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.523 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.627 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.619 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.568 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.415 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.416 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.368 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.386 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.544 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.640 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.718 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.386 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.420 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.639 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.695 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.707 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.619 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.595 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.530 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.402 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.510 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.448 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.432 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.408 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.382 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.415 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.420 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.599 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.601 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.405 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.385 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.601 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.736 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.489 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.693 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.441 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.386 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.562 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.469 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.433 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.426 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.493 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.559 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.400 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.442 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.537 |
MOD_SUMO_rev_2 | 119 | 125 | PF00179 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.369 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.776 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I9R5 | Leishmania donovani | 100% | 100% |
A4H7L3 | Leishmania braziliensis | 28% | 74% |
E9APP9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9APQ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 74% |