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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QAX3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.429 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.577 |
CLV_PCSK_FUR_1 | 342 | 346 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 344 | 346 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 388 | 394 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.758 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.548 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.523 |
DOC_CYCLIN_RxL_1 | 211 | 222 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 313 | 323 | PF00069 | 0.334 |
DOC_MAPK_gen_1 | 411 | 418 | PF00069 | 0.607 |
DOC_MAPK_MEF2A_6 | 411 | 418 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 57 | 64 | PF00069 | 0.358 |
DOC_MAPK_NFAT4_5 | 411 | 419 | PF00069 | 0.624 |
DOC_MAPK_RevD_3 | 60 | 75 | PF00069 | 0.368 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.627 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.459 |
LIG_14-3-3_CanoR_1 | 130 | 139 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 392 | 398 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 74 | 78 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.344 |
LIG_Actin_WH2_2 | 174 | 190 | PF00022 | 0.440 |
LIG_APCC_ABBA_1 | 333 | 338 | PF00400 | 0.378 |
LIG_BIR_III_4 | 79 | 83 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.263 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.477 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.455 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.585 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.442 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.246 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.427 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.595 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.565 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.427 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.396 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.644 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.581 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.395 |
LIG_LIR_Gen_1 | 24 | 29 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 320 | 329 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 85 | 94 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 43 | 47 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.331 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.350 |
LIG_Pex14_2 | 380 | 384 | PF04695 | 0.606 |
LIG_SH2_PTP2 | 136 | 139 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 334 | 337 | PF00017 | 0.363 |
LIG_SH2_SRC | 126 | 129 | PF00017 | 0.429 |
LIG_SH2_SRC | 136 | 139 | PF00017 | 0.436 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.314 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 372 | 375 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.338 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.507 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.366 |
LIG_SUMO_SIM_anti_2 | 277 | 284 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 325 | 331 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.380 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.550 |
LIG_TYR_ITIM | 332 | 337 | PF00017 | 0.363 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.348 |
LIG_TYR_ITIM | 92 | 97 | PF00017 | 0.347 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.485 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.559 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.402 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.458 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.595 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.578 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.439 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.683 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.624 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.741 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.783 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.491 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.553 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.519 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.695 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.709 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.644 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.470 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.507 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.397 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.378 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.364 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.363 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.453 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.430 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.600 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.544 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.481 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.540 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.630 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.622 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.387 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.345 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.590 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.296 |
MOD_Plk_2-3 | 284 | 290 | PF00069 | 0.491 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.434 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.296 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.355 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.641 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.433 |
MOD_SUMO_for_1 | 315 | 318 | PF00179 | 0.461 |
MOD_SUMO_for_1 | 40 | 43 | PF00179 | 0.492 |
MOD_SUMO_rev_2 | 104 | 111 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 196 | 200 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 310 | 315 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 409 | 419 | PF00179 | 0.658 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_2 | 212 | 218 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.652 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N9 | Leptomonas seymouri | 77% | 99% |
A0A0S4IV95 | Bodo saltans | 54% | 100% |
A0A1X0NKJ2 | Trypanosomatidae | 64% | 99% |
A0A3Q8ICV4 | Leishmania donovani | 93% | 100% |
A4HD65 | Leishmania braziliensis | 82% | 100% |
A4I0N0 | Leishmania infantum | 94% | 100% |
D0A6X8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 99% |
E9AWJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BW05 | Trypanosoma cruzi | 64% | 94% |