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: Q4QHV1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 264 | 270 | PF00089 | 0.593 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.520 |
CLV_PCSK_FUR_1 | 542 | 546 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 544 | 546 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 578 | 580 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.632 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.681 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.602 |
DOC_CYCLIN_RxL_1 | 322 | 331 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 33 | 42 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 182 | 191 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 325 | 332 | PF00069 | 0.519 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 235 | 238 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 209 | 216 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 400 | 406 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 412 | 421 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 481 | 491 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 591 | 599 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 613 | 621 | PF00244 | 0.624 |
LIG_Actin_WH2_2 | 335 | 351 | PF00022 | 0.539 |
LIG_Actin_WH2_2 | 406 | 424 | PF00022 | 0.568 |
LIG_AP2alpha_1 | 282 | 286 | PF02296 | 0.600 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.584 |
LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.523 |
LIG_eIF4E_1 | 317 | 323 | PF01652 | 0.422 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.509 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.591 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.551 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.537 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.478 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.553 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.611 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.623 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.521 |
LIG_GBD_Chelix_1 | 293 | 301 | PF00786 | 0.587 |
LIG_GBD_Chelix_1 | 318 | 326 | PF00786 | 0.438 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 608 | 619 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 50 | 54 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.492 |
LIG_Pex14_2 | 282 | 286 | PF04695 | 0.648 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.443 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.541 |
LIG_SH2_PTP2 | 380 | 383 | PF00017 | 0.496 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 602 | 605 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.579 |
LIG_SH3_1 | 190 | 196 | PF00018 | 0.642 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.614 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.642 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.515 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.639 |
LIG_Sin3_3 | 319 | 326 | PF02671 | 0.437 |
LIG_SUMO_SIM_anti_2 | 382 | 387 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 326 | 331 | PF11976 | 0.513 |
LIG_TRAF2_1 | 287 | 290 | PF00917 | 0.522 |
LIG_TYR_ITIM | 322 | 327 | PF00017 | 0.431 |
LIG_TYR_ITIM | 49 | 54 | PF00017 | 0.482 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.658 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.645 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.516 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.612 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.578 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.386 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.565 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.610 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.686 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.524 |
MOD_CMANNOS | 174 | 177 | PF00535 | 0.481 |
MOD_Cter_Amidation | 576 | 579 | PF01082 | 0.614 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.598 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.524 |
MOD_GlcNHglycan | 27 | 31 | PF01048 | 0.511 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.670 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.533 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.543 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.540 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.627 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.661 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.710 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.735 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.578 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.627 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.729 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.713 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.674 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.565 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.468 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.835 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.594 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.632 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.538 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.518 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.670 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.543 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.461 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.602 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.408 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.536 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.701 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.670 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.614 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.664 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.555 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.569 |
MOD_NEK2_2 | 567 | 572 | PF00069 | 0.493 |
MOD_PIKK_1 | 590 | 596 | PF00454 | 0.550 |
MOD_PIKK_1 | 601 | 607 | PF00454 | 0.475 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.587 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.609 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.549 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.487 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.662 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.535 |
MOD_Plk_1 | 580 | 586 | PF00069 | 0.638 |
MOD_Plk_2-3 | 435 | 441 | PF00069 | 0.595 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.533 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.615 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.608 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.638 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.638 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.554 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.590 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.655 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.524 |
MOD_SUMO_for_1 | 416 | 419 | PF00179 | 0.556 |
TRG_DiLeu_BaEn_4 | 471 | 477 | PF01217 | 0.647 |
TRG_DiLeu_BaLyEn_6 | 343 | 348 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 487 | 492 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 600 | 603 | PF00928 | 0.706 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 481 | 484 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.524 |
TRG_NES_CRM1_1 | 376 | 390 | PF08389 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 164 | 169 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 346 | 350 | PF00026 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILV8 | Leptomonas seymouri | 38% | 100% |
A0A3S7WQR1 | Leishmania donovani | 90% | 100% |
A4H5Q4 | Leishmania braziliensis | 68% | 96% |
A4HTZ4 | Leishmania infantum | 90% | 100% |
E9AMS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |