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: 32 |
NetGPI | no | yes: 0, no: 32 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
Related structures:
AlphaFold database: Q4Q310
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.740 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.620 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.664 |
CLV_Separin_Metazoa | 125 | 129 | PF03568 | 0.672 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.560 |
DEG_APCC_DBOX_1 | 383 | 391 | PF00400 | 0.429 |
DOC_CYCLIN_RxL_1 | 211 | 219 | PF00134 | 0.625 |
DOC_CYCLIN_yCln2_LP_2 | 506 | 512 | PF00134 | 0.329 |
DOC_CYCLIN_yCln2_LP_2 | 640 | 646 | PF00134 | 0.364 |
DOC_MAPK_DCC_7 | 467 | 477 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 14 | 22 | PF00069 | 0.700 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 413 | 423 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 195 | 202 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 237 | 246 | PF00069 | 0.574 |
DOC_PP1_RVXF_1 | 519 | 526 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 506 | 509 | PF13499 | 0.393 |
DOC_PP2B_LxvP_1 | 596 | 599 | PF13499 | 0.481 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.720 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.681 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 38 | 42 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 462 | 467 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 559 | 566 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 608 | 614 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 95 | 103 | PF00244 | 0.770 |
LIG_Actin_WH2_2 | 421 | 438 | PF00022 | 0.367 |
LIG_BIR_III_4 | 622 | 626 | PF00653 | 0.429 |
LIG_BRCT_BRCA1_1 | 611 | 615 | PF00533 | 0.441 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.634 |
LIG_Clathr_ClatBox_1 | 423 | 427 | PF01394 | 0.346 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.658 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.592 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.528 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.734 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.412 |
LIG_Integrin_RGD_1 | 140 | 142 | PF01839 | 0.494 |
LIG_LIR_Apic_2 | 524 | 529 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 188 | 193 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 579 | 588 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 7 | 18 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 524 | 528 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 579 | 583 | PF02991 | 0.420 |
LIG_PDZ_Class_2 | 659 | 664 | PF00595 | 0.417 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.589 |
LIG_SH2_CRK | 526 | 530 | PF00017 | 0.388 |
LIG_SH2_CRK | 580 | 584 | PF00017 | 0.454 |
LIG_SH2_CRK | 641 | 645 | PF00017 | 0.409 |
LIG_SH2_NCK_1 | 641 | 645 | PF00017 | 0.404 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.558 |
LIG_SH2_SRC | 539 | 542 | PF00017 | 0.498 |
LIG_SH2_SRC | 641 | 644 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 580 | 584 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 336 | 339 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.356 |
LIG_SH3_2 | 599 | 604 | PF14604 | 0.387 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.673 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.411 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.392 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.676 |
LIG_Sin3_3 | 144 | 151 | PF02671 | 0.634 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.699 |
LIG_SUMO_SIM_anti_2 | 240 | 246 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 260 | 266 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 419 | 425 | PF11976 | 0.341 |
LIG_SUMO_SIM_anti_2 | 491 | 498 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 545 | 551 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.678 |
LIG_SUMO_SIM_par_1 | 491 | 498 | PF11976 | 0.327 |
LIG_TYR_ITIM | 578 | 583 | PF00017 | 0.526 |
LIG_TYR_ITIM | 639 | 644 | PF00017 | 0.460 |
LIG_UBA3_1 | 190 | 195 | PF00899 | 0.583 |
MOD_CAAXbox | 661 | 664 | PF01239 | 0.520 |
MOD_CDC14_SPxK_1 | 601 | 604 | PF00782 | 0.445 |
MOD_CDC14_SPxK_1 | 79 | 82 | PF00782 | 0.592 |
MOD_CDK_SPK_2 | 76 | 81 | PF00069 | 0.593 |
MOD_CDK_SPxK_1 | 598 | 604 | PF00069 | 0.475 |
MOD_CDK_SPxK_1 | 76 | 82 | PF00069 | 0.596 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.661 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.650 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.512 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.610 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.490 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.507 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.477 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.510 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.411 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.651 |
MOD_Cter_Amidation | 129 | 132 | PF01082 | 0.619 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.804 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.678 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.624 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.494 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.666 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.652 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.595 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.514 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.520 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.589 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.636 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.638 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.485 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.527 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.621 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.594 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.687 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.496 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.413 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.508 |
MOD_OFUCOSY | 37 | 44 | PF10250 | 0.561 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.545 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.663 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.569 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.570 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.591 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.654 |
MOD_PKB_1 | 478 | 486 | PF00069 | 0.438 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.546 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.510 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.533 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.508 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.444 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.534 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.419 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.597 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.592 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.589 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.751 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.455 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.475 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.605 |
TRG_DiLeu_BaEn_1 | 240 | 245 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.474 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_1 | 419 | 424 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_1 | 491 | 496 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 641 | 644 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.625 |
TRG_NES_CRM1_1 | 263 | 276 | PF08389 | 0.542 |
TRG_NES_CRM1_1 | 433 | 448 | PF08389 | 0.434 |
TRG_NLS_MonoExtN_4 | 212 | 217 | PF00514 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 63% | 100% |
A0A0N1PB02 | Leptomonas seymouri | 40% | 100% |
A0A0S4J6C6 | Bodo saltans | 37% | 100% |
A0A1X0P9A6 | Trypanosomatidae | 36% | 97% |
A0A3Q8IHH1 | Leishmania donovani | 83% | 91% |
A0A3R7K2Y9 | Trypanosoma rangeli | 39% | 97% |
A0A3S5H668 | Leishmania donovani | 38% | 100% |
A0A3S5H669 | Leishmania donovani | 38% | 100% |
A0A3S7X835 | Leishmania donovani | 41% | 100% |
A4H5C9 | Leishmania braziliensis | 38% | 100% |
A4H5D0 | Leishmania braziliensis | 40% | 100% |
A4HAZ7 | Leishmania braziliensis | 41% | 100% |
A4HAZ9 | Leishmania braziliensis | 42% | 100% |
A4HB01 | Leishmania braziliensis | 43% | 100% |
A4HTM0 | Leishmania infantum | 38% | 100% |
A4HTM1 | Leishmania infantum | 38% | 100% |
A4IA57 | Leishmania infantum | 41% | 100% |
C6K3V8 | Leptomonas seymouri | 38% | 100% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 98% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4Q1U8 | Leishmania major | 99% | 100% |
Q4Q2R4 | Leishmania major | 40% | 100% |
Q4Q312 | Leishmania major | 100% | 100% |
Q4Q340 | Leishmania major | 100% | 100% |
Q4Q342 | Leishmania major | 100% | 100% |
Q4QI90 | Leishmania major | 38% | 100% |
Q4QI91 | Leishmania major | 37% | 100% |