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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4H5W5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.462 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.534 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.499 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.554 |
DEG_SCF_FBW7_1 | 518 | 525 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.506 |
DEG_SPOP_SBC_1 | 435 | 439 | PF00917 | 0.466 |
DEG_SPOP_SBC_1 | 44 | 48 | PF00917 | 0.655 |
DOC_CYCLIN_RxL_1 | 422 | 434 | PF00134 | 0.611 |
DOC_CYCLIN_RxL_1 | 459 | 468 | PF00134 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 257 | 263 | PF00134 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 303 | 309 | PF00134 | 0.315 |
DOC_MAPK_DCC_7 | 251 | 261 | PF00069 | 0.518 |
DOC_MAPK_HePTP_8 | 348 | 360 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 351 | 360 | PF00069 | 0.501 |
DOC_MAPK_NFAT4_5 | 351 | 359 | PF00069 | 0.543 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.579 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.361 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.575 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 209 | 218 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 381 | 389 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 568 | 573 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.607 |
LIG_Actin_WH2_2 | 113 | 130 | PF00022 | 0.545 |
LIG_APCC_ABBA_1 | 547 | 552 | PF00400 | 0.399 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.576 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 65 | 69 | PF00533 | 0.579 |
LIG_CaM_NSCaTE_8 | 452 | 459 | PF13499 | 0.549 |
LIG_Clathr_ClatBox_1 | 394 | 398 | PF01394 | 0.396 |
LIG_Clathr_ClatBox_1 | 464 | 468 | PF01394 | 0.410 |
LIG_EH1_1 | 423 | 431 | PF00400 | 0.599 |
LIG_EVH1_2 | 276 | 280 | PF00568 | 0.405 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.555 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.601 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.697 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.485 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.578 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.379 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.514 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.568 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 321 | 327 | PF02991 | 0.580 |
LIG_LIR_Apic_2 | 391 | 396 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 116 | 123 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 193 | 204 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 490 | 495 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 116 | 120 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.554 |
LIG_NRBOX | 245 | 251 | PF00104 | 0.497 |
LIG_PAM2_1 | 314 | 326 | PF00658 | 0.344 |
LIG_PCNA_yPIPBox_3 | 240 | 250 | PF02747 | 0.599 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 340 | 344 | PF00017 | 0.607 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.698 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 362 | 365 | PF00017 | 0.559 |
LIG_SH2_STAT3 | 457 | 460 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.698 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 503 | 509 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 462 | 468 | PF11976 | 0.460 |
LIG_TRAF2_1 | 571 | 574 | PF00917 | 0.499 |
LIG_TYR_ITIM | 307 | 312 | PF00017 | 0.517 |
LIG_UBA3_1 | 463 | 469 | PF00899 | 0.509 |
LIG_UBA3_1 | 506 | 514 | PF00899 | 0.544 |
MOD_CDK_SPxK_1 | 518 | 524 | PF00069 | 0.594 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.659 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.688 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.676 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.697 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.687 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.581 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.588 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.678 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.630 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.518 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.450 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.536 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.500 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.618 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.605 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.701 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.489 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.446 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.698 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.516 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.524 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.437 |
MOD_GlcNHglycan | 451 | 455 | PF01048 | 0.475 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.470 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.713 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.596 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.529 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.603 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.642 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.736 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.683 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.600 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.600 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.699 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.510 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.589 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.737 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.513 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.597 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.461 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.433 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.578 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.600 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.678 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.473 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.613 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.521 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.591 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.692 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.467 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.536 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.647 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.501 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.494 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.494 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.613 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.479 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.692 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.608 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.569 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.608 |
MOD_PK_1 | 568 | 574 | PF00069 | 0.490 |
MOD_PKA_1 | 28 | 34 | PF00069 | 0.573 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.639 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.664 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.602 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.539 |
MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.664 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.561 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.713 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.334 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.477 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.288 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.518 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.527 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.506 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.681 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.618 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.594 |
TRG_DiLeu_BaEn_1 | 512 | 517 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 425 | 430 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 459 | 464 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2L4 | Leptomonas seymouri | 54% | 96% |
A0A3Q8I8N5 | Leishmania donovani | 81% | 100% |
A0A3R7NSE1 | Trypanosoma rangeli | 29% | 100% |
A4HU60 | Leishmania infantum | 81% | 100% |
D0A9P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AMZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QHN7 | Leishmania major | 82% | 100% |
V5BMK0 | Trypanosoma cruzi | 28% | 100% |