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: A4HTZ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 263 | 269 | PF00089 | 0.583 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.614 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 577 | 579 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.544 |
DEG_APCC_DBOX_1 | 369 | 377 | PF00400 | 0.407 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.671 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.528 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.570 |
DOC_CYCLIN_RxL_1 | 321 | 330 | PF00134 | 0.445 |
DOC_MAPK_gen_1 | 33 | 42 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 71 | 78 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 324 | 331 | PF00069 | 0.512 |
DOC_PP4_FxxP_1 | 234 | 237 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.549 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 208 | 215 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 399 | 405 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 411 | 420 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 482 | 488 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 590 | 598 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 612 | 620 | PF00244 | 0.587 |
LIG_Actin_WH2_2 | 334 | 350 | PF00022 | 0.530 |
LIG_Actin_WH2_2 | 405 | 423 | PF00022 | 0.517 |
LIG_AP2alpha_1 | 281 | 285 | PF02296 | 0.521 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.563 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.500 |
LIG_Clathr_ClatBox_1 | 212 | 216 | PF01394 | 0.498 |
LIG_eIF4E_1 | 316 | 322 | PF01652 | 0.418 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.485 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.539 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.550 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.634 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.473 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.484 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.512 |
LIG_GBD_Chelix_1 | 292 | 300 | PF00786 | 0.527 |
LIG_GBD_Chelix_1 | 317 | 325 | PF00786 | 0.436 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 607 | 618 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 343 | 347 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 50 | 54 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 607 | 613 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.486 |
LIG_Pex14_2 | 281 | 285 | PF04695 | 0.521 |
LIG_PTAP_UEV_1 | 555 | 560 | PF05743 | 0.565 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.450 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.528 |
LIG_SH2_PTP2 | 379 | 382 | PF00017 | 0.473 |
LIG_SH2_SRC | 379 | 382 | PF00017 | 0.421 |
LIG_SH2_STAT3 | 601 | 604 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.558 |
LIG_SH3_1 | 189 | 195 | PF00018 | 0.619 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.570 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.619 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.494 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.627 |
LIG_Sin3_3 | 318 | 325 | PF02671 | 0.438 |
LIG_SUMO_SIM_anti_2 | 381 | 386 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 246 | 253 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 325 | 330 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 508 | 513 | PF11976 | 0.563 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.475 |
LIG_TYR_ITIM | 321 | 326 | PF00017 | 0.439 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.468 |
MOD_CDK_SPK_2 | 233 | 238 | PF00069 | 0.480 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.598 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.616 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.485 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.579 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.521 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.387 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.531 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.671 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.512 |
MOD_CMANNOS | 173 | 176 | PF00535 | 0.515 |
MOD_Cter_Amidation | 575 | 578 | PF01082 | 0.741 |
MOD_DYRK1A_RPxSP_1 | 191 | 195 | PF00069 | 0.545 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.582 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.500 |
MOD_GlcNHglycan | 27 | 31 | PF01048 | 0.443 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.682 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.456 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.535 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.604 |
MOD_GlcNHglycan | 462 | 466 | PF01048 | 0.593 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.573 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.650 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.646 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.705 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.644 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.539 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.589 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.655 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.592 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.571 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.552 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.430 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.771 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.679 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.623 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.504 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.501 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.659 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.502 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.477 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.459 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.685 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.520 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.587 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.574 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.570 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.647 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.544 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.585 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.515 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.409 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.584 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.544 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.457 |
MOD_PK_1 | 72 | 78 | PF00069 | 0.476 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.476 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.536 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.595 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.472 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.636 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.472 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.522 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.629 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.483 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.576 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.556 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.608 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.629 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.524 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.546 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.499 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.644 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.507 |
MOD_SUMO_for_1 | 415 | 418 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 511 | 520 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 66 | 74 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_4 | 470 | 476 | PF01217 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 342 | 347 | PF01217 | 0.446 |
TRG_DiLeu_BaLyEn_6 | 486 | 491 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.611 |
TRG_NES_CRM1_1 | 375 | 389 | PF08389 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 324 | 328 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILV8 | Leptomonas seymouri | 38% | 100% |
A0A3S7WQR1 | Leishmania donovani | 100% | 100% |
A4H5Q4 | Leishmania braziliensis | 69% | 100% |
E9AMS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QHV1 | Leishmania major | 90% | 100% |