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: A4HH66
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.529 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.554 |
DEG_SPOP_SBC_1 | 371 | 375 | PF00917 | 0.512 |
DEG_SPOP_SBC_1 | 389 | 393 | PF00917 | 0.711 |
DOC_MAPK_gen_1 | 113 | 121 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 184 | 195 | PF00069 | 0.531 |
DOC_MAPK_RevD_3 | 417 | 431 | PF00069 | 0.556 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.512 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 284 | 288 | PF12436 | 0.566 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 226 | 233 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 369 | 379 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 472 | 479 | PF00244 | 0.557 |
LIG_eIF4E_1 | 171 | 177 | PF01652 | 0.517 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.593 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.676 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.378 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.552 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.665 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.552 |
LIG_GBD_Chelix_1 | 452 | 460 | PF00786 | 0.525 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 415 | 419 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.569 |
LIG_MYND_1 | 190 | 194 | PF01753 | 0.501 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.587 |
LIG_SH2_NCK_1 | 94 | 98 | PF00017 | 0.447 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.555 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.600 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.580 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.447 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 343 | 349 | PF11976 | 0.486 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.648 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.629 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.536 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.708 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.501 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.648 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.660 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.686 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.677 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.541 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.713 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.624 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.464 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.592 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.805 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.574 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.552 |
MOD_Cter_Amidation | 123 | 126 | PF01082 | 0.353 |
MOD_Cter_Amidation | 284 | 287 | PF01082 | 0.550 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.743 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.744 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.656 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.556 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.598 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.689 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.709 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.495 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.490 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.674 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.802 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.706 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.504 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.687 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.655 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.517 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.612 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.584 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.524 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.543 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.604 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.600 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.517 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.588 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.500 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.565 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.601 |
MOD_PKB_1 | 115 | 123 | PF00069 | 0.387 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.531 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.535 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.654 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.628 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.549 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.408 |
MOD_Plk_2-3 | 435 | 441 | PF00069 | 0.628 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.385 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.511 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.534 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.506 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.740 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.631 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.509 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.677 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.668 |
MOD_SUMO_rev_2 | 312 | 322 | PF00179 | 0.627 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.614 |
TRG_NLS_Bipartite_1 | 131 | 149 | PF00514 | 0.348 |
TRG_NLS_MonoCore_2 | 395 | 400 | PF00514 | 0.550 |
TRG_NLS_MonoExtC_3 | 395 | 400 | PF00514 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 430 | 434 | PF00026 | 0.572 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCW8 | Leptomonas seymouri | 38% | 97% |
A0A3Q8IF08 | Leishmania donovani | 65% | 99% |
A4I4B0 | Leishmania infantum | 64% | 99% |
E9ADR0 | Leishmania major | 64% | 100% |
E9AM20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 63% | 100% |