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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H394
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.803 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.796 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 381 | 385 | PF00917 | 0.789 |
DEG_SPOP_SBC_1 | 77 | 81 | PF00917 | 0.570 |
DOC_MAPK_gen_1 | 275 | 284 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 344 | 351 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 448 | 455 | PF00069 | 0.643 |
DOC_PP1_RVXF_1 | 452 | 458 | PF00149 | 0.639 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.758 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 17 | 21 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 382 | 392 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 419 | 426 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.579 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.543 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.543 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.543 |
LIG_BIR_III_4 | 352 | 356 | PF00653 | 0.703 |
LIG_CtBP_PxDLS_1 | 213 | 217 | PF00389 | 0.556 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.540 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.595 |
LIG_FHA_1 | 473 | 479 | PF00498 | 0.581 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 431 | 435 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 132 | 140 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 410 | 414 | PF02991 | 0.623 |
LIG_SH2_GRB2like | 411 | 414 | PF00017 | 0.726 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.477 |
LIG_SH2_SRC | 261 | 264 | PF00017 | 0.427 |
LIG_SH2_SRC | 432 | 435 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.555 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.576 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.573 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.529 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.563 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.702 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.614 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.639 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.649 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.558 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.533 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.801 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.572 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.694 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.552 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.752 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.735 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.633 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.605 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.453 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.669 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.647 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.782 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.810 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.678 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.546 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.667 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.626 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.681 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.716 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.713 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.699 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.618 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.534 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.502 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.706 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.656 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.669 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.647 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.577 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.464 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.588 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.709 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.762 |
MOD_N-GLC_2 | 413 | 415 | PF02516 | 0.548 |
MOD_N-GLC_2 | 421 | 423 | PF02516 | 0.521 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.465 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.556 |
MOD_NEK2_2 | 436 | 441 | PF00069 | 0.476 |
MOD_OFUCOSY | 417 | 423 | PF10250 | 0.744 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.529 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.557 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.573 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.800 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.600 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.589 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.800 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.597 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.782 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.791 |
MOD_PKB_1 | 474 | 482 | PF00069 | 0.579 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.494 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.570 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.677 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.670 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.405 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.702 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.532 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.626 |
MOD_SUMO_for_1 | 211 | 214 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_1 | 451 | 456 | PF01217 | 0.631 |
TRG_DiLeu_LyEn_5 | 451 | 456 | PF01217 | 0.631 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.803 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 473 | 476 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 175 | 179 | PF00026 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 454 | 459 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCB0 | Leptomonas seymouri | 43% | 93% |
A0A451EJD3 | Leishmania donovani | 61% | 94% |
A4HRK2 | Leishmania infantum | 61% | 94% |
E9AC70 | Leishmania major | 57% | 99% |
E9AJG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 97% |