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 |
Related structures:
AlphaFold database: Q4QAH2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.654 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.762 |
CLV_PCSK_FUR_1 | 181 | 185 | PF00082 | 0.494 |
CLV_PCSK_FUR_1 | 378 | 382 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.733 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.726 |
CLV_PCSK_PC7_1 | 373 | 379 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.564 |
CLV_Separin_Metazoa | 162 | 166 | PF03568 | 0.455 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.558 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.483 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.509 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 521 | 527 | PF00134 | 0.565 |
DOC_MAPK_DCC_7 | 357 | 366 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 143 | 152 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 143 | 152 | PF00069 | 0.450 |
DOC_MAPK_NFAT4_5 | 143 | 151 | PF00069 | 0.451 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.543 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.684 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.583 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 122 | 131 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 357 | 362 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 543 | 549 | PF00244 | 0.490 |
LIG_Actin_WH2_2 | 360 | 375 | PF00022 | 0.666 |
LIG_Actin_WH2_2 | 8 | 26 | PF00022 | 0.545 |
LIG_BIR_III_4 | 396 | 400 | PF00653 | 0.671 |
LIG_deltaCOP1_diTrp_1 | 205 | 210 | PF00928 | 0.472 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.630 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.703 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.638 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.454 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.471 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.554 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.603 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.706 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.579 |
LIG_FHA_2 | 545 | 551 | PF00498 | 0.517 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.558 |
LIG_GBD_Chelix_1 | 50 | 58 | PF00786 | 0.503 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.501 |
LIG_LYPXL_yS_3 | 19 | 22 | PF13949 | 0.585 |
LIG_MYND_1 | 309 | 313 | PF01753 | 0.599 |
LIG_MYND_1 | 514 | 518 | PF01753 | 0.573 |
LIG_NRBOX | 11 | 17 | PF00104 | 0.491 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.607 |
LIG_SH2_STAT3 | 256 | 259 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.597 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.488 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.649 |
LIG_SUMO_SIM_anti_2 | 192 | 198 | PF11976 | 0.477 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.446 |
LIG_TRAF2_1 | 392 | 395 | PF00917 | 0.602 |
LIG_TYR_ITSM | 15 | 22 | PF00017 | 0.393 |
MOD_CDC14_SPxK_1 | 503 | 506 | PF00782 | 0.599 |
MOD_CDK_SPK_2 | 305 | 310 | PF00069 | 0.575 |
MOD_CDK_SPxK_1 | 500 | 506 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 399 | 406 | PF00069 | 0.664 |
MOD_CDK_SPxxK_3 | 492 | 499 | PF00069 | 0.608 |
MOD_CDK_SPxxK_3 | 514 | 521 | PF00069 | 0.588 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.579 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.566 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.709 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.739 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.784 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.668 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.553 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.709 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.572 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.751 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.655 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.578 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.448 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.547 |
MOD_CMANNOS | 528 | 531 | PF00535 | 0.601 |
MOD_Cter_Amidation | 181 | 184 | PF01082 | 0.489 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.428 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.617 |
MOD_GlcNHglycan | 247 | 252 | PF01048 | 0.592 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.616 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.502 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.589 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.596 |
MOD_GlcNHglycan | 46 | 50 | PF01048 | 0.579 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.562 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.641 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.494 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.700 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.716 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.617 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.777 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.536 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.635 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.645 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.511 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.459 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.587 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.718 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.706 |
MOD_N-GLC_1 | 504 | 509 | PF02516 | 0.674 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.428 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.309 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.426 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.596 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.624 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.470 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.603 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.593 |
MOD_PK_1 | 63 | 69 | PF00069 | 0.467 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.421 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.617 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.448 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.536 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.474 |
MOD_PKB_1 | 379 | 387 | PF00069 | 0.734 |
MOD_PKB_1 | 43 | 51 | PF00069 | 0.449 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.650 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.715 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.549 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.652 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.343 |
MOD_Plk_2-3 | 324 | 330 | PF00069 | 0.565 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.422 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.495 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.591 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.720 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.619 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.692 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.757 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.693 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.658 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.566 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.533 |
MOD_SUMO_rev_2 | 400 | 407 | PF00179 | 0.661 |
TRG_DiLeu_BaEn_2 | 361 | 367 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.597 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.760 |
TRG_ER_diArg_1 | 543 | 546 | PF00400 | 0.538 |
TRG_NES_CRM1_1 | 317 | 329 | PF08389 | 0.665 |
TRG_NES_CRM1_1 | 56 | 71 | PF08389 | 0.398 |
TRG_NLS_MonoCore_2 | 375 | 380 | PF00514 | 0.726 |
TRG_NLS_MonoExtC_3 | 375 | 380 | PF00514 | 0.726 |
TRG_NLS_MonoExtN_4 | 373 | 380 | PF00514 | 0.727 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WYG0 | Leishmania donovani | 87% | 100% |
A4HDL9 | Leishmania braziliensis | 66% | 99% |
E9AH66 | Leishmania infantum | 87% | 100% |
E9AX04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |