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: E9AKC0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.690 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.588 |
DEG_SPOP_SBC_1 | 229 | 233 | PF00917 | 0.647 |
DOC_MAPK_gen_1 | 441 | 448 | PF00069 | 0.599 |
DOC_MAPK_MEF2A_6 | 441 | 448 | PF00069 | 0.552 |
DOC_PP1_RVXF_1 | 280 | 287 | PF00149 | 0.543 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.761 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.751 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.785 |
LIG_14-3-3_CanoR_1 | 151 | 156 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 261 | 269 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 392 | 399 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 67 | 74 | PF00244 | 0.477 |
LIG_APCC_ABBAyCdc20_2 | 5 | 11 | PF00400 | 0.716 |
LIG_DLG_GKlike_1 | 282 | 289 | PF00625 | 0.436 |
LIG_eIF4E_1 | 198 | 204 | PF01652 | 0.584 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.675 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.418 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.591 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.563 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.588 |
LIG_FXI_DFP_1 | 270 | 274 | PF00024 | 0.388 |
LIG_LIR_Gen_1 | 272 | 279 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 285 | 291 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 285 | 289 | PF02991 | 0.551 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.717 |
LIG_SH3_1 | 223 | 229 | PF00018 | 0.690 |
LIG_SH3_2 | 164 | 169 | PF14604 | 0.752 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.788 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.740 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.722 |
LIG_Sin3_3 | 315 | 322 | PF02671 | 0.470 |
LIG_SUMO_SIM_anti_2 | 285 | 291 | PF11976 | 0.649 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.753 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.675 |
LIG_TRAF2_1 | 383 | 386 | PF00917 | 0.629 |
LIG_WRC_WIRS_1 | 152 | 157 | PF05994 | 0.536 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.545 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.689 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.678 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.747 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.816 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.620 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.489 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.695 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.656 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.781 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.694 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.670 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.616 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.591 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.657 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.737 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.832 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.630 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.645 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.713 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.538 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.599 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.496 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.785 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.689 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.639 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.683 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.626 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.724 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.689 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.652 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.583 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.621 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.542 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.625 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.671 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.708 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.686 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.834 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.664 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.561 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.671 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.557 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.585 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.753 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.544 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.563 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.519 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.668 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.726 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.718 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.647 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.719 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.575 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.397 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.439 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.353 |
MOD_PIKK_1 | 391 | 397 | PF00454 | 0.542 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.549 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.661 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.542 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.507 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.756 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.717 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.721 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.664 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.781 |
MOD_SUMO_rev_2 | 54 | 62 | PF00179 | 0.605 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.467 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 299 | 303 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.687 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKE8 | Leptomonas seymouri | 40% | 97% |
A0A3S7WNZ9 | Leishmania donovani | 83% | 100% |
A4H462 | Leishmania braziliensis | 72% | 100% |
A4HSD1 | Leishmania infantum | 83% | 100% |
Q4QJI7 | Leishmania major | 83% | 100% |