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: A0A3S7WSI1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.390 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 623 | 627 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.531 |
CLV_Separin_Metazoa | 148 | 152 | PF03568 | 0.413 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.541 |
DEG_SCF_FBW7_1 | 401 | 406 | PF00400 | 0.529 |
DEG_SCF_FBW7_1 | 603 | 610 | PF00400 | 0.429 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.742 |
DOC_CYCLIN_yCln2_LP_2 | 46 | 49 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.413 |
DOC_PP1_RVXF_1 | 302 | 309 | PF00149 | 0.366 |
DOC_PP1_RVXF_1 | 581 | 588 | PF00149 | 0.412 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.605 |
DOC_PP4_MxPP_1 | 509 | 512 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.688 |
DOC_USP7_UBL2_3 | 211 | 215 | PF12436 | 0.538 |
DOC_USP7_UBL2_3 | 461 | 465 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.748 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 256 | 266 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 452 | 460 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 88 | 97 | PF00244 | 0.537 |
LIG_AP2alpha_1 | 572 | 576 | PF02296 | 0.438 |
LIG_APCC_ABBA_1 | 372 | 377 | PF00400 | 0.579 |
LIG_APCC_ABBA_1 | 614 | 619 | PF00400 | 0.355 |
LIG_BIR_III_4 | 357 | 361 | PF00653 | 0.656 |
LIG_Clathr_ClatBox_1 | 522 | 526 | PF01394 | 0.360 |
LIG_EVH1_1 | 510 | 514 | PF00568 | 0.397 |
LIG_EVH1_2 | 530 | 534 | PF00568 | 0.367 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.587 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.621 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.631 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.569 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.551 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.569 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.646 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.559 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.385 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.531 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.272 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.633 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.511 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.589 |
LIG_GBD_Chelix_1 | 179 | 187 | PF00786 | 0.372 |
LIG_GBD_Chelix_1 | 569 | 577 | PF00786 | 0.486 |
LIG_LIR_Gen_1 | 500 | 510 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 549 | 560 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 571 | 580 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 571 | 575 | PF02991 | 0.427 |
LIG_Pex14_2 | 534 | 538 | PF04695 | 0.364 |
LIG_Pex14_2 | 572 | 576 | PF04695 | 0.541 |
LIG_REV1ctd_RIR_1 | 573 | 582 | PF16727 | 0.440 |
LIG_SH2_CRK | 542 | 546 | PF00017 | 0.381 |
LIG_SH2_GRB2like | 317 | 320 | PF00017 | 0.418 |
LIG_SH2_GRB2like | 548 | 551 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 552 | 556 | PF00017 | 0.394 |
LIG_SH2_PTP2 | 502 | 505 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.417 |
LIG_SH2_STAT3 | 617 | 620 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.673 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.420 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.363 |
LIG_SUMO_SIM_anti_2 | 260 | 267 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 524 | 529 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 521 | 526 | PF11976 | 0.359 |
LIG_SxIP_EBH_1 | 259 | 270 | PF03271 | 0.387 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.409 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.585 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.726 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.686 |
LIG_TYR_ITAM | 539 | 555 | PF00017 | 0.396 |
LIG_UBA3_1 | 276 | 284 | PF00899 | 0.369 |
LIG_UBA3_1 | 307 | 313 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 569 | 574 | PF05994 | 0.373 |
MOD_CDK_SPK_2 | 562 | 567 | PF00069 | 0.437 |
MOD_CDK_SPK_2 | 83 | 88 | PF00069 | 0.544 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.522 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.339 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.410 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.689 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.701 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.637 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.417 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.642 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.643 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.595 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.683 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.611 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.703 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.531 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.363 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.642 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.641 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.608 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.648 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.709 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.635 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.648 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.752 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.609 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.522 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.727 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.716 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.576 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.542 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.555 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.624 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.430 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.614 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.557 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.610 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.732 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.592 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.578 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.429 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.660 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.382 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.408 |
MOD_N-GLC_2 | 161 | 163 | PF02516 | 0.429 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.397 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.518 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.451 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.392 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.660 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.430 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.390 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.564 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.396 |
MOD_PIKK_1 | 601 | 607 | PF00454 | 0.539 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.578 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.594 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.614 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.687 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.403 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.426 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.526 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.458 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.389 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.334 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.529 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.600 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.471 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.402 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.782 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.421 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.524 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.613 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.439 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.434 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.747 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 214 | 219 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 298 | 306 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 63 | 71 | PF00179 | 0.604 |
TRG_DiLeu_BaEn_1 | 145 | 150 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_1 | 208 | 213 | PF01217 | 0.441 |
TRG_DiLeu_BaEn_2 | 387 | 393 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.377 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM83 | Leptomonas seymouri | 56% | 100% |
A4H785 | Leishmania braziliensis | 77% | 99% |
A4HVM5 | Leishmania infantum | 100% | 100% |
E9APC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 97% |
Q4QG57 | Leishmania major | 92% | 100% |