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: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 4 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q3U3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.633 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.696 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.598 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.721 |
DOC_MAPK_gen_1 | 465 | 473 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 98 | 108 | PF00069 | 0.584 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.719 |
DOC_USP7_UBL2_3 | 283 | 287 | PF12436 | 0.629 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.811 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 206 | 211 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 226 | 236 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 371 | 378 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 381 | 385 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 427 | 435 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 439 | 444 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 479 | 484 | PF00244 | 0.648 |
LIG_Actin_WH2_2 | 195 | 213 | PF00022 | 0.478 |
LIG_BIR_III_2 | 239 | 243 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.713 |
LIG_CtBP_PxDLS_1 | 489 | 493 | PF00389 | 0.547 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.759 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.510 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.638 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.593 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.651 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.799 |
LIG_LIR_Gen_1 | 420 | 426 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 482 | 492 | PF02991 | 0.666 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.671 |
LIG_LYPXL_SIV_4 | 168 | 176 | PF13949 | 0.498 |
LIG_MYND_3 | 111 | 115 | PF01753 | 0.488 |
LIG_PCNA_yPIPBox_3 | 188 | 199 | PF02747 | 0.553 |
LIG_PTB_Apo_2 | 163 | 170 | PF02174 | 0.381 |
LIG_PTB_Phospho_1 | 163 | 169 | PF10480 | 0.380 |
LIG_SH2_GRB2like | 384 | 387 | PF00017 | 0.724 |
LIG_SH2_SRC | 169 | 172 | PF00017 | 0.500 |
LIG_SH2_SRC | 384 | 387 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.587 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.581 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.600 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.570 |
LIG_TRAF2_1 | 215 | 218 | PF00917 | 0.637 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.655 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.631 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.679 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.614 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.612 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.565 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.675 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.670 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.662 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.728 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.621 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.613 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.593 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.462 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.687 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.767 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.540 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.626 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.646 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.590 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.791 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.511 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.649 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.666 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.711 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.682 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.807 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.739 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.711 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.575 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.761 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.728 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.632 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.579 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.594 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.584 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.734 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.769 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.676 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.654 |
MOD_PKA_1 | 427 | 433 | PF00069 | 0.705 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.569 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.719 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.626 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.635 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.711 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.634 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.561 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.580 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.689 |
MOD_Plk_2-3 | 43 | 49 | PF00069 | 0.707 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.714 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.762 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.801 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.812 |
MOD_SUMO_rev_2 | 238 | 248 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 350 | 354 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 99 | 106 | PF00179 | 0.624 |
TRG_DiLeu_BaEn_3 | 420 | 426 | PF01217 | 0.518 |
TRG_DiLeu_BaEn_4 | 185 | 191 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.706 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 2 | 6 | PF00026 | 0.673 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.644 |
TRG_Pf-PMV_PEXEL_1 | 98 | 102 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMH4 | Leptomonas seymouri | 66% | 100% |
A0A1X0P3T7 | Trypanosomatidae | 38% | 100% |
A0A3S7X729 | Leishmania donovani | 91% | 100% |
A0A422P039 | Trypanosoma rangeli | 36% | 100% |
A4HLV5 | Leishmania braziliensis | 57% | 99% |
E9AHR2 | Leishmania infantum | 91% | 100% |
E9B483 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |