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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 6 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q661
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.681 |
CLV_C14_Caspase3-7 | 396 | 400 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.709 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.550 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.703 |
DEG_SPOP_SBC_1 | 308 | 312 | PF00917 | 0.746 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.701 |
DOC_CKS1_1 | 144 | 149 | PF01111 | 0.749 |
DOC_CKS1_1 | 540 | 545 | PF01111 | 0.741 |
DOC_MAPK_MEF2A_6 | 432 | 441 | PF00069 | 0.660 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.689 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.728 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.745 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.728 |
LIG_14-3-3_CanoR_1 | 234 | 244 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.675 |
LIG_deltaCOP1_diTrp_1 | 232 | 240 | PF00928 | 0.695 |
LIG_DLG_GKlike_1 | 534 | 542 | PF00625 | 0.702 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.825 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.822 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.715 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.768 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.653 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.657 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.853 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.740 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.697 |
LIG_NRBOX | 226 | 232 | PF00104 | 0.694 |
LIG_PTAP_UEV_1 | 485 | 490 | PF05743 | 0.633 |
LIG_REV1ctd_RIR_1 | 357 | 366 | PF16727 | 0.733 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.701 |
LIG_SH2_STAP1 | 465 | 469 | PF00017 | 0.679 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.694 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.650 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.746 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.648 |
LIG_SH3_3 | 540 | 546 | PF00018 | 0.738 |
LIG_SUMO_SIM_anti_2 | 592 | 598 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 330 | 335 | PF11976 | 0.697 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.653 |
LIG_TRAF2_1 | 567 | 570 | PF00917 | 0.666 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.720 |
MOD_CDK_SPK_2 | 539 | 544 | PF00069 | 0.745 |
MOD_CDK_SPxK_1 | 143 | 149 | PF00069 | 0.678 |
MOD_CDK_SPxxK_3 | 143 | 150 | PF00069 | 0.720 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.721 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.645 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.718 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.711 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.678 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.707 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.756 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.753 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.726 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.731 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.681 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.727 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.714 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.737 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.710 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.686 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.854 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.776 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.709 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.684 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.484 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.566 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.516 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.460 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.454 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.542 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.502 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.496 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.559 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.529 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.429 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.457 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.544 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.471 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.482 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.452 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.495 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.460 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.521 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.369 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.488 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.698 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.700 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.820 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.712 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.731 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.803 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.622 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.708 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.744 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.768 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.726 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.662 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.677 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.647 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.711 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.670 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.723 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.640 |
MOD_LATS_1 | 532 | 538 | PF00433 | 0.700 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.476 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.483 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.503 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.513 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.680 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.705 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.707 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.789 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.700 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.648 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.676 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.630 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.730 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.644 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.735 |
MOD_PIKK_1 | 348 | 354 | PF00454 | 0.751 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.714 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.716 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.706 |
MOD_PIKK_1 | 536 | 542 | PF00454 | 0.723 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.729 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.695 |
MOD_PKB_1 | 420 | 428 | PF00069 | 0.664 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.719 |
MOD_Plk_1 | 518 | 524 | PF00069 | 0.715 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.672 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.695 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.641 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.712 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.722 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.645 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.802 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.770 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.756 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.720 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.733 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.710 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.745 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.702 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.738 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.701 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.743 |
MOD_SUMO_rev_2 | 565 | 573 | PF00179 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 69 | 74 | PF01217 | 0.714 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.694 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.700 |
TRG_ER_diArg_1 | 147 | 150 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 549 | 552 | PF00400 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4Q2 | Leishmania donovani | 89% | 100% |
A4HJI3 | Leishmania braziliensis | 54% | 99% |
A4I732 | Leishmania infantum | 89% | 85% |
E9B200 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |