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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
Related structures:
AlphaFold database: A0A3Q8ISH4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.839 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.446 |
CLV_PCSK_FUR_1 | 26 | 30 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 394 | 396 | PF00082 | 0.454 |
CLV_PCSK_PC7_1 | 24 | 30 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 330 | 336 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.587 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.486 |
DOC_MAPK_DCC_7 | 591 | 599 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 146 | 156 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 296 | 304 | PF00069 | 0.603 |
DOC_MAPK_MEF2A_6 | 149 | 158 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 499 | 506 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 591 | 599 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 77 | 86 | PF00069 | 0.318 |
DOC_PIKK_1 | 75 | 82 | PF02985 | 0.387 |
DOC_PP1_RVXF_1 | 501 | 507 | PF00149 | 0.280 |
DOC_PP1_RVXF_1 | 93 | 100 | PF00149 | 0.344 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.591 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.655 |
DOC_PP4_FxxP_1 | 316 | 319 | PF00568 | 0.604 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.503 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.393 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 503 | 509 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.352 |
LIG_Actin_WH2_2 | 75 | 93 | PF00022 | 0.441 |
LIG_APCC_ABBA_1 | 617 | 622 | PF00400 | 0.518 |
LIG_APCC_ABBAyCdc20_2 | 616 | 622 | PF00400 | 0.517 |
LIG_BH_BH3_1 | 441 | 457 | PF00452 | 0.346 |
LIG_BIR_III_4 | 556 | 560 | PF00653 | 0.283 |
LIG_BRCT_BRCA1_1 | 437 | 441 | PF00533 | 0.465 |
LIG_Clathr_ClatBox_1 | 129 | 133 | PF01394 | 0.292 |
LIG_eIF4E_1 | 113 | 119 | PF01652 | 0.370 |
LIG_eIF4E_1 | 612 | 618 | PF01652 | 0.529 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.372 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.494 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.564 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.432 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.336 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.432 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.417 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.368 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.577 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.735 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.742 |
LIG_GBD_Chelix_1 | 432 | 440 | PF00786 | 0.412 |
LIG_LIR_Apic_2 | 314 | 319 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 171 | 179 | PF02991 | 0.801 |
LIG_LIR_Gen_1 | 434 | 445 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 579 | 589 | PF02991 | 0.356 |
LIG_LIR_LC3C_4 | 517 | 521 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.796 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 607 | 612 | PF02991 | 0.357 |
LIG_MAD2 | 70 | 78 | PF02301 | 0.353 |
LIG_NRBOX | 435 | 441 | PF00104 | 0.277 |
LIG_PCNA_PIPBox_1 | 348 | 357 | PF02747 | 0.590 |
LIG_PCNA_yPIPBox_3 | 347 | 355 | PF02747 | 0.608 |
LIG_PCNA_yPIPBox_3 | 524 | 534 | PF02747 | 0.258 |
LIG_Pex14_2 | 312 | 316 | PF04695 | 0.572 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.413 |
LIG_Pex14_2 | 460 | 464 | PF04695 | 0.389 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.620 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.629 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.618 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.662 |
LIG_SH2_PTP2 | 115 | 118 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 531 | 535 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 582 | 586 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 609 | 613 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.467 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.500 |
LIG_SUMO_SIM_anti_2 | 517 | 523 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 532 | 537 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 600 | 607 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 447 | 454 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 491 | 496 | PF11976 | 0.632 |
LIG_SUMO_SIM_par_1 | 82 | 87 | PF11976 | 0.428 |
LIG_SxIP_EBH_1 | 416 | 426 | PF03271 | 0.519 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.674 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.698 |
LIG_TYR_ITSM | 109 | 116 | PF00017 | 0.371 |
LIG_UBA3_1 | 417 | 422 | PF00899 | 0.487 |
LIG_UBA3_1 | 515 | 524 | PF00899 | 0.318 |
LIG_WRC_WIRS_1 | 291 | 296 | PF05994 | 0.457 |
LIG_WRC_WIRS_1 | 457 | 462 | PF05994 | 0.541 |
LIG_WRC_WIRS_1 | 465 | 470 | PF05994 | 0.452 |
MOD_CDK_SPxxK_3 | 84 | 91 | PF00069 | 0.452 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.351 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.303 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.549 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.546 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.439 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.682 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.715 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.518 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.745 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.635 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.651 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.510 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.442 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.503 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.405 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.621 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.598 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.437 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.395 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.719 |
MOD_LATS_1 | 278 | 284 | PF00433 | 0.438 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.530 |
MOD_N-GLC_2 | 566 | 568 | PF02516 | 0.522 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.340 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.717 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.757 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.569 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.438 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.415 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.263 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.474 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.331 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.333 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.399 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.499 |
MOD_NEK2_2 | 424 | 429 | PF00069 | 0.492 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.677 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.289 |
MOD_PKA_1 | 280 | 286 | PF00069 | 0.496 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.501 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.598 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.588 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.504 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.532 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.471 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.309 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.534 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.479 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.372 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.455 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.366 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.379 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.357 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.421 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.613 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.713 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.473 |
MOD_SUMO_for_1 | 387 | 390 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 133 | 142 | PF00179 | 0.454 |
MOD_SUMO_rev_2 | 389 | 396 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 87 | 93 | PF00179 | 0.479 |
TRG_DiLeu_BaEn_1 | 376 | 381 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 489 | 494 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 26 | 29 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2M1 | Leptomonas seymouri | 39% | 100% |
A0A0N1HRT9 | Leptomonas seymouri | 36% | 100% |
A0A0N1P9A0 | Leptomonas seymouri | 33% | 100% |
A0A0N1PBU6 | Leptomonas seymouri | 37% | 100% |
A0A1X0P9W4 | Trypanosomatidae | 32% | 100% |
A0A3Q8IFF3 | Leishmania donovani | 70% | 99% |
A0A3S7X483 | Leishmania donovani | 50% | 97% |
A0A3S7X888 | Leishmania donovani | 33% | 99% |
A4HB26 | Leishmania braziliensis | 34% | 100% |
A4HJ59 | Leishmania braziliensis | 41% | 100% |
A4HJ60 | Leishmania braziliensis | 55% | 100% |
A4I6H4 | Leishmania infantum | 50% | 100% |
A4I6H5 | Leishmania infantum | 99% | 100% |
A4IA83 | Leishmania infantum | 33% | 100% |
C9ZM24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B1N2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9B1N3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9B596 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q4Q6I2 | Leishmania major | 90% | 100% |
Q4Q6I3 | Leishmania major | 51% | 100% |