Uncharacterized Protein, Uncharacterized
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IAH6
Term | Name | Level | Count |
---|---|---|---|
GO:0044145 | modulation of formation of structure involved in a symbiotic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.678 |
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.775 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.541 |
CLV_PCSK_FUR_1 | 27 | 31 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 639 | 641 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.693 |
CLV_Separin_Metazoa | 197 | 201 | PF03568 | 0.373 |
DEG_APCC_DBOX_1 | 432 | 440 | PF00400 | 0.727 |
DEG_APCC_DBOX_1 | 484 | 492 | PF00400 | 0.483 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.662 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.710 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.711 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.578 |
DOC_MAPK_gen_1 | 102 | 110 | PF00069 | 0.616 |
DOC_MAPK_gen_1 | 432 | 438 | PF00069 | 0.634 |
DOC_MAPK_gen_1 | 609 | 615 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 624 | 632 | PF00069 | 0.660 |
DOC_MAPK_MEF2A_6 | 286 | 293 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 353 | 360 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 624 | 632 | PF00069 | 0.623 |
DOC_MAPK_NFAT4_5 | 286 | 294 | PF00069 | 0.455 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.519 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.644 |
DOC_PP4_FxxP_1 | 593 | 596 | PF00568 | 0.743 |
DOC_PP4_FxxP_1 | 670 | 673 | PF00568 | 0.692 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.644 |
DOC_USP7_UBL2_3 | 660 | 664 | PF12436 | 0.765 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 582 | 587 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 600 | 606 | PF00244 | 0.647 |
LIG_Actin_WH2_2 | 196 | 213 | PF00022 | 0.455 |
LIG_Actin_WH2_2 | 474 | 491 | PF00022 | 0.497 |
LIG_BRCT_BRCA1_1 | 447 | 451 | PF00533 | 0.666 |
LIG_BRCT_BRCA1_1 | 589 | 593 | PF00533 | 0.755 |
LIG_CaM_IQ_9 | 561 | 576 | PF13499 | 0.574 |
LIG_EH1_1 | 481 | 489 | PF00400 | 0.559 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.680 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.446 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.573 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.614 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.520 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.451 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.710 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.512 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.621 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.481 |
LIG_GBD_Chelix_1 | 343 | 351 | PF00786 | 0.517 |
LIG_LIR_Apic_2 | 590 | 596 | PF02991 | 0.718 |
LIG_LIR_Apic_2 | 81 | 86 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 116 | 123 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.515 |
LIG_NRBOX | 189 | 195 | PF00104 | 0.460 |
LIG_NRBOX | 71 | 77 | PF00104 | 0.568 |
LIG_PDZ_Class_2 | 671 | 676 | PF00595 | 0.701 |
LIG_Pex14_2 | 670 | 674 | PF04695 | 0.687 |
LIG_Rb_LxCxE_1 | 238 | 259 | PF01857 | 0.621 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 218 | 221 | PF00017 | 0.497 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.676 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.544 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.503 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.649 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.668 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.742 |
LIG_SH3_4 | 660 | 667 | PF00018 | 0.626 |
LIG_SUMO_SIM_anti_2 | 180 | 189 | PF11976 | 0.518 |
LIG_SUMO_SIM_anti_2 | 228 | 235 | PF11976 | 0.512 |
LIG_SUMO_SIM_anti_2 | 57 | 63 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 89 | 94 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.645 |
LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 531 | 539 | PF11976 | 0.610 |
LIG_TRAF2_1 | 476 | 479 | PF00917 | 0.558 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.570 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.740 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.557 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.717 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.703 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.688 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.519 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.532 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.567 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.505 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.671 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.573 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.644 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.513 |
MOD_Cter_Amidation | 129 | 132 | PF01082 | 0.567 |
MOD_Cter_Amidation | 430 | 433 | PF01082 | 0.733 |
MOD_Cter_Amidation | 637 | 640 | PF01082 | 0.698 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.496 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.576 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.730 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.732 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.432 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.512 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.625 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.700 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.682 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.682 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.455 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.650 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.692 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.527 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.658 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.668 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.723 |
MOD_LATS_1 | 580 | 586 | PF00433 | 0.609 |
MOD_LATS_1 | 95 | 101 | PF00433 | 0.410 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.637 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.631 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.569 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.418 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.346 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.411 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.553 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.589 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.682 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.469 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.505 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.525 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.617 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.696 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.565 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.409 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.605 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.661 |
MOD_PK_1 | 156 | 162 | PF00069 | 0.693 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.623 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.644 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.599 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.647 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.739 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.510 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.596 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.712 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.622 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.629 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.597 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.606 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.538 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.568 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.696 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.769 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.559 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.666 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.655 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.570 |
TRG_DiLeu_BaEn_1 | 181 | 186 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.540 |
TRG_DiLeu_BaEn_2 | 105 | 111 | PF01217 | 0.624 |
TRG_DiLeu_BaEn_2 | 610 | 616 | PF01217 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 482 | 487 | PF01217 | 0.571 |
TRG_DiLeu_LyEn_5 | 71 | 76 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.643 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.709 |
TRG_NES_CRM1_1 | 181 | 195 | PF08389 | 0.458 |
TRG_NLS_MonoExtC_3 | 35 | 41 | PF00514 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 614 | 618 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E6 | Leptomonas seymouri | 49% | 100% |
A0A0S4KLZ0 | Bodo saltans | 27% | 85% |
A0A1X0PAG6 | Trypanosomatidae | 35% | 100% |
A0A3Q8IIY0 | Leishmania donovani | 100% | 100% |
A0A422NVB5 | Trypanosoma rangeli | 32% | 100% |
A4HBC8 | Leishmania braziliensis | 73% | 100% |
C9ZLR4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B5K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q2D6 | Leishmania major | 90% | 98% |
V5BRF7 | Trypanosoma cruzi | 33% | 100% |