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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QG55
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.791 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.768 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.752 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.808 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.608 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.809 |
CLV_PCSK_FUR_1 | 468 | 472 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.752 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.556 |
CLV_PCSK_PC7_1 | 396 | 402 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 68 | 74 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.647 |
DOC_ANK_TNKS_1 | 309 | 316 | PF00023 | 0.699 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.789 |
DOC_MAPK_gen_1 | 323 | 330 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 425 | 432 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 245 | 251 | PF00149 | 0.452 |
DOC_PP1_RVXF_1 | 324 | 331 | PF00149 | 0.648 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.710 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.684 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.643 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.532 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.651 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 383 | 390 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 461 | 467 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 72 | 77 | PF00244 | 0.526 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.624 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.701 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.635 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.584 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.743 |
LIG_Integrin_RGD_1 | 310 | 312 | PF01839 | 0.701 |
LIG_LIR_Gen_1 | 357 | 367 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.639 |
LIG_PDZ_Class_2 | 485 | 490 | PF00595 | 0.620 |
LIG_SH2_NCK_1 | 359 | 363 | PF00017 | 0.650 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.533 |
LIG_SH3_2 | 128 | 133 | PF14604 | 0.708 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.718 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.733 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.773 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 360 | 366 | PF11976 | 0.564 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.646 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.566 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.447 |
LIG_UBA3_1 | 58 | 65 | PF00899 | 0.669 |
MOD_CDK_SPxxK_3 | 21 | 28 | PF00069 | 0.564 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.687 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.644 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.809 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.693 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.690 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.582 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.601 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.474 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.642 |
MOD_GlcNHglycan | 142 | 147 | PF01048 | 0.682 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.629 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.780 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.569 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.540 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.725 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.713 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.714 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.727 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.644 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.570 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.645 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.694 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.688 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.649 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.609 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.543 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.714 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.457 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.758 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.636 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.656 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.619 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.576 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.651 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.635 |
MOD_PKB_1 | 292 | 300 | PF00069 | 0.765 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.627 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.564 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.796 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.567 |
MOD_SUMO_for_1 | 482 | 485 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 24 | 33 | PF00179 | 0.653 |
MOD_SUMO_rev_2 | 450 | 458 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 473 | 480 | PF00179 | 0.694 |
TRG_DiLeu_BaEn_1 | 410 | 415 | PF01217 | 0.594 |
TRG_DiLeu_BaEn_4 | 453 | 459 | PF01217 | 0.432 |
TRG_DiLeu_LyEn_5 | 410 | 415 | PF01217 | 0.626 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.645 |
TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.650 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.597 |
TRG_NLS_Bipartite_1 | 3 | 20 | PF00514 | 0.672 |
TRG_NLS_MonoCore_2 | 128 | 133 | PF00514 | 0.708 |
TRG_NLS_MonoCore_2 | 289 | 294 | PF00514 | 0.807 |
TRG_NLS_MonoExtC_3 | 128 | 133 | PF00514 | 0.735 |
TRG_NLS_MonoExtC_3 | 223 | 228 | PF00514 | 0.630 |
TRG_NLS_MonoExtC_3 | 289 | 294 | PF00514 | 0.749 |
TRG_NLS_MonoExtC_3 | 346 | 352 | PF00514 | 0.664 |
TRG_NLS_MonoExtN_4 | 128 | 133 | PF00514 | 0.729 |
TRG_NLS_MonoExtN_4 | 224 | 231 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 28 | 35 | PF00514 | 0.612 |
TRG_NLS_MonoExtN_4 | 345 | 351 | PF00514 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 456 | 460 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE43 | Leptomonas seymouri | 54% | 97% |
A0A3S7WSJ6 | Leishmania donovani | 90% | 100% |
A0A422NGB0 | Trypanosoma rangeli | 37% | 100% |
A4H787 | Leishmania braziliensis | 69% | 98% |
A4HVM7 | Leishmania infantum | 90% | 100% |
D0A6M7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9APC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5AVQ1 | Trypanosoma cruzi | 34% | 100% |