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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: A0A3S7X888
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.774 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.475 |
CLV_PCSK_PC7_1 | 338 | 344 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.283 |
DEG_APCC_DBOX_1 | 381 | 389 | PF00400 | 0.560 |
DOC_CYCLIN_RxL_1 | 532 | 545 | PF00134 | 0.269 |
DOC_CYCLIN_yCln2_LP_2 | 104 | 110 | PF00134 | 0.528 |
DOC_MAPK_DCC_7 | 599 | 607 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 152 | 160 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 599 | 607 | PF00069 | 0.287 |
DOC_MAPK_RevD_3 | 386 | 402 | PF00069 | 0.502 |
DOC_PP1_RVXF_1 | 122 | 129 | PF00149 | 0.531 |
DOC_PP1_RVXF_1 | 307 | 313 | PF00149 | 0.613 |
DOC_PP1_RVXF_1 | 535 | 542 | PF00149 | 0.266 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.587 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.242 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.769 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.553 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 360 | 370 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.736 |
LIG_14-3-3_CanoR_1 | 496 | 500 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 537 | 542 | PF00244 | 0.287 |
LIG_Actin_WH2_2 | 104 | 122 | PF00022 | 0.645 |
LIG_Clathr_ClatBox_1 | 388 | 392 | PF01394 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 27 | 30 | PF00928 | 0.614 |
LIG_EH1_1 | 625 | 633 | PF00400 | 0.581 |
LIG_eIF4E_1 | 596 | 602 | PF01652 | 0.268 |
LIG_eIF4E_1 | 620 | 626 | PF01652 | 0.524 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.546 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.629 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.554 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.486 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.234 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.165 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.408 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.698 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.552 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.652 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.685 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.567 |
LIG_GBD_Chelix_1 | 628 | 636 | PF00786 | 0.421 |
LIG_LIR_Apic_2 | 322 | 327 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 318 | 327 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 534 | 542 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 618 | 628 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 534 | 538 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.350 |
LIG_LYPXL_S_1 | 472 | 476 | PF13949 | 0.377 |
LIG_LYPXL_yS_3 | 473 | 476 | PF13949 | 0.377 |
LIG_PCNA_yPIPBox_3 | 590 | 599 | PF02747 | 0.260 |
LIG_Pex14_2 | 248 | 252 | PF04695 | 0.615 |
LIG_Pex14_2 | 320 | 324 | PF04695 | 0.560 |
LIG_Pex14_2 | 612 | 616 | PF04695 | 0.454 |
LIG_PTAP_UEV_1 | 76 | 81 | PF05743 | 0.642 |
LIG_SH2_CRK | 413 | 417 | PF00017 | 0.624 |
LIG_SH2_GRB2like | 221 | 224 | PF00017 | 0.704 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 535 | 539 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 555 | 558 | PF00017 | 0.361 |
LIG_SH2_STAT3 | 587 | 590 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.521 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.639 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.364 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.706 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.688 |
LIG_SUMO_SIM_anti_2 | 153 | 159 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 437 | 442 | PF11976 | 0.276 |
LIG_SUMO_SIM_anti_2 | 446 | 452 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 478 | 483 | PF11976 | 0.270 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.665 |
LIG_TRAF2_1 | 381 | 384 | PF00917 | 0.498 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.567 |
LIG_UBA3_1 | 146 | 152 | PF00899 | 0.458 |
LIG_UBA3_1 | 388 | 396 | PF00899 | 0.526 |
LIG_WRC_WIRS_1 | 299 | 304 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 44 | 49 | PF05994 | 0.628 |
LIG_WRC_WIRS_1 | 538 | 543 | PF05994 | 0.378 |
LIG_WRC_WIRS_1 | 612 | 617 | PF05994 | 0.274 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.522 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.789 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.352 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.567 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.693 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.716 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.688 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.562 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.369 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.538 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.559 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.428 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.528 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.524 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.490 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.507 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.590 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.662 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.568 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.541 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.399 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.367 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.366 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.685 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.367 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.323 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.368 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.528 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.407 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.543 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.742 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.761 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.569 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.509 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.491 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.558 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.540 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.325 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.316 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.548 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.369 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.397 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.545 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.607 |
MOD_NEK2_2 | 488 | 493 | PF00069 | 0.287 |
MOD_NEK2_2 | 566 | 571 | PF00069 | 0.452 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.681 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.520 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.545 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.622 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.525 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.601 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.355 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.552 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.777 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.681 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.567 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.515 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.518 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.358 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.333 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.291 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.337 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.367 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.357 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.350 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.588 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.596 |
MOD_SUMO_rev_2 | 115 | 122 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 392 | 398 | PF00179 | 0.601 |
TRG_DiLeu_BaEn_1 | 153 | 158 | PF01217 | 0.587 |
TRG_DiLeu_BaEn_1 | 264 | 269 | PF01217 | 0.710 |
TRG_DiLeu_BaEn_1 | 384 | 389 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_4 | 165 | 171 | PF01217 | 0.623 |
TRG_DiLeu_BaEn_4 | 86 | 92 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 534 | 539 | PF01217 | 0.269 |
TRG_DiLeu_LyEn_5 | 109 | 114 | PF01217 | 0.567 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.511 |
TRG_NLS_MonoExtC_3 | 395 | 400 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 393 | 400 | PF00514 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2M1 | Leptomonas seymouri | 31% | 100% |
A0A0N1HRT9 | Leptomonas seymouri | 31% | 100% |
A0A0N1P9A0 | Leptomonas seymouri | 30% | 100% |
A0A0N1PBU6 | Leptomonas seymouri | 54% | 100% |
A0A1X0P9W4 | Trypanosomatidae | 37% | 100% |
A0A3Q8IFF3 | Leishmania donovani | 32% | 98% |
A0A3Q8ISH4 | Leishmania donovani | 33% | 100% |
A0A3R7KFP4 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X483 | Leishmania donovani | 32% | 98% |
A4HB26 | Leishmania braziliensis | 67% | 99% |
A4HJ59 | Leishmania braziliensis | 30% | 100% |
A4HJ60 | Leishmania braziliensis | 31% | 100% |
A4I6H4 | Leishmania infantum | 32% | 98% |
A4I6H5 | Leishmania infantum | 33% | 100% |
A4IA83 | Leishmania infantum | 99% | 100% |
C9ZM24 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B1N2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1N3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B596 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q6I2 | Leishmania major | 34% | 100% |
Q4Q6I3 | Leishmania major | 31% | 99% |
V5B5A9 | Trypanosoma cruzi | 37% | 100% |