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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4HBE1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.504 |
CLV_PCSK_FUR_1 | 460 | 464 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 370 | 378 | PF00400 | 0.518 |
DEG_SCF_FBW7_1 | 109 | 115 | PF00400 | 0.527 |
DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.521 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.742 |
DOC_CKS1_1 | 109 | 114 | PF01111 | 0.684 |
DOC_CYCLIN_RxL_1 | 129 | 138 | PF00134 | 0.285 |
DOC_CYCLIN_yCln2_LP_2 | 344 | 350 | PF00134 | 0.413 |
DOC_MAPK_gen_1 | 266 | 276 | PF00069 | 0.232 |
DOC_MAPK_gen_1 | 504 | 510 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 269 | 278 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 8 | 16 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 344 | 347 | PF13499 | 0.407 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.689 |
DOC_PP4_FxxP_1 | 530 | 533 | PF00568 | 0.411 |
DOC_SPAK_OSR1_1 | 299 | 303 | PF12202 | 0.505 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.731 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.459 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 189 | 194 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 269 | 275 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 319 | 326 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 460 | 469 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 521 | 530 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 78 | 82 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.775 |
LIG_Actin_WH2_2 | 271 | 286 | PF00022 | 0.397 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.405 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 255 | 261 | PF00928 | 0.474 |
LIG_EH1_1 | 234 | 242 | PF00400 | 0.249 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.286 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.755 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.492 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.284 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.787 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.655 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.489 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.625 |
LIG_LIR_Apic_2 | 42 | 48 | PF02991 | 0.585 |
LIG_LIR_Apic_2 | 528 | 533 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 154 | 162 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 272 | 283 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 341 | 350 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 384 | 390 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 464 | 472 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 534 | 541 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 254 | 259 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 443 | 448 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 464 | 469 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 534 | 538 | PF02991 | 0.511 |
LIG_MYND_1 | 119 | 123 | PF01753 | 0.636 |
LIG_MYND_1 | 58 | 62 | PF01753 | 0.743 |
LIG_Pex14_1 | 257 | 261 | PF04695 | 0.474 |
LIG_Pex14_1 | 296 | 300 | PF04695 | 0.399 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.419 |
LIG_Pex14_2 | 445 | 449 | PF04695 | 0.457 |
LIG_PTB_Apo_2 | 305 | 312 | PF02174 | 0.489 |
LIG_PTB_Apo_2 | 444 | 451 | PF02174 | 0.519 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.513 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.435 |
LIG_SH2_CRK | 535 | 539 | PF00017 | 0.557 |
LIG_SH2_GRB2like | 306 | 309 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 250 | 254 | PF00017 | 0.471 |
LIG_SH2_SRC | 359 | 362 | PF00017 | 0.494 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.422 |
LIG_SH2_SRC | 515 | 518 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.760 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.505 |
LIG_SH3_1 | 147 | 153 | PF00018 | 0.567 |
LIG_SH3_1 | 38 | 44 | PF00018 | 0.480 |
LIG_SH3_2 | 150 | 155 | PF14604 | 0.599 |
LIG_SH3_2 | 73 | 78 | PF14604 | 0.744 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.503 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.489 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.731 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.359 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.722 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.771 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.751 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.718 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.749 |
LIG_TYR_ITIM | 280 | 285 | PF00017 | 0.416 |
LIG_TYR_ITIM | 287 | 292 | PF00017 | 0.435 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.413 |
LIG_WW_2 | 23 | 26 | PF00397 | 0.519 |
LIG_WW_3 | 75 | 79 | PF00397 | 0.750 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.470 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.450 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.479 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.448 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.491 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.704 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.347 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.447 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.443 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.469 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.713 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.697 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.526 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.674 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.672 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.672 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.355 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.479 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.528 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.412 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.688 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.665 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.556 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.465 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.791 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.488 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.525 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.366 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.412 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.399 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.376 |
MOD_PKA_1 | 319 | 325 | PF00069 | 0.269 |
MOD_PKA_1 | 462 | 468 | PF00069 | 0.421 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.596 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.330 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.743 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.697 |
MOD_PKB_1 | 460 | 468 | PF00069 | 0.401 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.529 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.504 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.410 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.497 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.426 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.521 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.588 |
MOD_Plk_2-3 | 528 | 534 | PF00069 | 0.482 |
MOD_Plk_2-3 | 543 | 549 | PF00069 | 0.580 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.445 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.368 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.422 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.418 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.373 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.373 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.402 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.439 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.657 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.691 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.641 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.414 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.731 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.659 |
MOD_SUMO_rev_2 | 138 | 146 | PF00179 | 0.504 |
TRG_DiLeu_BaEn_4 | 542 | 548 | PF01217 | 0.585 |
TRG_DiLeu_BaLyEn_6 | 478 | 483 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.521 |
TRG_NES_CRM1_1 | 125 | 138 | PF08389 | 0.546 |
TRG_NES_CRM1_1 | 379 | 394 | PF08389 | 0.407 |
TRG_NLS_Bipartite_1 | 356 | 374 | PF00514 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 35 | 39 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.270 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5V7 | Leptomonas seymouri | 68% | 95% |
A0A0S4IP10 | Bodo saltans | 26% | 100% |
A0A0S4J2A0 | Bodo saltans | 28% | 67% |
A0A0S4KMJ1 | Bodo saltans | 48% | 100% |
A0A1X0NU11 | Trypanosomatidae | 26% | 100% |
A0A1X0PB74 | Trypanosomatidae | 57% | 100% |
A0A3S5IRZ3 | Trypanosoma rangeli | 52% | 100% |
A0A3S7X8K5 | Leishmania donovani | 82% | 95% |
A4IAI9 | Leishmania infantum | 82% | 95% |
C9ZLP9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZS63 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 85% |
E9B5L3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 95% |
Q4Q2C3 | Leishmania major | 82% | 100% |
V5BQ23 | Trypanosoma cruzi | 24% | 100% |
V5BRE4 | Trypanosoma cruzi | 56% | 100% |