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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9B5A4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.449 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.436 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.724 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.741 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.499 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.598 |
DEG_SCF_FBW7_1 | 35 | 41 | PF00400 | 0.472 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.435 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.465 |
DOC_CYCLIN_RxL_1 | 303 | 315 | PF00134 | 0.358 |
DOC_CYCLIN_RxL_1 | 331 | 343 | PF00134 | 0.279 |
DOC_CYCLIN_RxL_1 | 84 | 97 | PF00134 | 0.295 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 198 | 205 | PF00134 | 0.277 |
DOC_MAPK_FxFP_2 | 187 | 190 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 196 | 205 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 304 | 312 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 377 | 385 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 282 | 291 | PF00069 | 0.479 |
DOC_PP2B_PxIxI_1 | 174 | 180 | PF00149 | 0.430 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.329 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.410 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 168 | 177 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 263 | 268 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 353 | 363 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 63 | 72 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.460 |
LIG_BIR_III_2 | 147 | 151 | PF00653 | 0.343 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 399 | 403 | PF00533 | 0.374 |
LIG_deltaCOP1_diTrp_1 | 262 | 268 | PF00928 | 0.330 |
LIG_eIF4E_1 | 204 | 210 | PF01652 | 0.482 |
LIG_EVH1_1 | 34 | 38 | PF00568 | 0.399 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.330 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.293 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.319 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.620 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.574 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 315 | 320 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.428 |
LIG_PDZ_Class_2 | 421 | 426 | PF00595 | 0.661 |
LIG_Pex14_1 | 184 | 188 | PF04695 | 0.325 |
LIG_Pex14_1 | 264 | 268 | PF04695 | 0.514 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.378 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.501 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 382 | 385 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.252 |
LIG_SH2_STAT3 | 141 | 144 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.401 |
LIG_SH3_1 | 317 | 323 | PF00018 | 0.401 |
LIG_SH3_1 | 32 | 38 | PF00018 | 0.414 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.583 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.384 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.401 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.385 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.407 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 336 | 343 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 336 | 343 | PF11976 | 0.273 |
LIG_TYR_ITIM | 267 | 272 | PF00017 | 0.387 |
MOD_CDK_SPK_2 | 316 | 321 | PF00069 | 0.405 |
MOD_CDK_SPxK_1 | 257 | 263 | PF00069 | 0.413 |
MOD_CDK_SPxxK_3 | 171 | 178 | PF00069 | 0.517 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.540 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.553 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.520 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.387 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.570 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.488 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.310 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.742 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.585 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.763 |
MOD_GlcNHglycan | 392 | 396 | PF01048 | 0.665 |
MOD_GlcNHglycan | 53 | 57 | PF01048 | 0.751 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.659 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.679 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.824 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.531 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.376 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.519 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.508 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.349 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.456 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.485 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.438 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.608 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.432 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.552 |
MOD_N-GLC_2 | 131 | 133 | PF02516 | 0.688 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.484 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.381 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.540 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.424 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.408 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.510 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.397 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.503 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.439 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.485 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.349 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.515 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.517 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.414 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.421 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.290 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.499 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.520 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.413 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.386 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.403 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.390 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.410 |
MOD_SUMO_rev_2 | 343 | 350 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 366 | 373 | PF00179 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.287 |
TRG_DiLeu_LyEn_5 | 172 | 177 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 135 | 138 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.352 |
TRG_NLS_MonoExtN_4 | 304 | 310 | PF00514 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.672 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHK0 | Leptomonas seymouri | 49% | 96% |
A0A3S7X898 | Leishmania donovani | 86% | 100% |
A4HB34 | Leishmania braziliensis | 71% | 100% |
A4IAN5 | Leishmania infantum | 86% | 100% |
Q4Q2M9 | Leishmania major | 85% | 100% |