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: E9AFG7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 489 | 493 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.472 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.594 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.379 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 56 | 58 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.663 |
DEG_APCC_DBOX_1 | 362 | 370 | PF00400 | 0.411 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.642 |
DOC_CDC14_PxL_1 | 322 | 330 | PF14671 | 0.375 |
DOC_CYCLIN_yCln2_LP_2 | 257 | 263 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 133 | 141 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 213 | 221 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 525 | 533 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 534 | 540 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 99 | 108 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 102 | 110 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 357 | 366 | PF00069 | 0.509 |
DOC_MIT_MIM_1 | 152 | 161 | PF04212 | 0.411 |
DOC_PP1_RVXF_1 | 218 | 224 | PF00149 | 0.507 |
DOC_PP1_SILK_1 | 359 | 364 | PF00149 | 0.515 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.513 |
DOC_USP7_UBL2_3 | 390 | 394 | PF12436 | 0.422 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 165 | 170 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 363 | 367 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 453 | 457 | PF00244 | 0.445 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.500 |
LIG_BRCT_BRCA1_1 | 545 | 549 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_2 | 50 | 56 | PF00533 | 0.492 |
LIG_deltaCOP1_diTrp_1 | 479 | 484 | PF00928 | 0.474 |
LIG_EH1_1 | 378 | 386 | PF00400 | 0.418 |
LIG_eIF4E_1 | 323 | 329 | PF01652 | 0.424 |
LIG_eIF4E_1 | 331 | 337 | PF01652 | 0.361 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.516 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.609 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.488 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.484 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.584 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.427 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.579 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.533 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.401 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.451 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.634 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.572 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 25 | 33 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 479 | 488 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 4 | 9 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 479 | 483 | PF02991 | 0.607 |
LIG_NRBOX | 267 | 273 | PF00104 | 0.518 |
LIG_NRBOX | 365 | 371 | PF00104 | 0.404 |
LIG_PDZ_Wminus1_1 | 584 | 586 | PF00595 | 0.540 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.427 |
LIG_SH2_SRC | 323 | 326 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.410 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.502 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.535 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.577 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.711 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.430 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 18 | 23 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 121 | 128 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 259 | 265 | PF11976 | 0.583 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 460 | 467 | PF11976 | 0.432 |
LIG_TRFH_1 | 278 | 282 | PF08558 | 0.550 |
LIG_TRFH_1 | 322 | 326 | PF08558 | 0.398 |
LIG_TYR_ITIM | 305 | 310 | PF00017 | 0.414 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.414 |
LIG_WRC_WIRS_1 | 537 | 542 | PF05994 | 0.488 |
MOD_CDK_SPK_2 | 397 | 402 | PF00069 | 0.608 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.645 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.566 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.606 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.465 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.550 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.502 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.729 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.472 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.490 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.588 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.524 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.509 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.461 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.694 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.515 |
MOD_GlcNHglycan | 33 | 37 | PF01048 | 0.598 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.561 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.453 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.351 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.530 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.531 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.602 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.641 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.551 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.368 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.553 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.614 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.496 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.583 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.427 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.480 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.681 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.634 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.381 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.521 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.598 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.523 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.609 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.590 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.522 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.392 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.549 |
MOD_LATS_1 | 351 | 357 | PF00433 | 0.564 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.439 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.522 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.501 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.650 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.525 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.503 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.458 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.457 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.621 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.397 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.354 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.655 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.497 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.398 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.590 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.479 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.598 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.488 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.642 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.504 |
MOD_PK_1 | 357 | 363 | PF00069 | 0.481 |
MOD_PK_1 | 525 | 531 | PF00069 | 0.440 |
MOD_PKA_1 | 165 | 171 | PF00069 | 0.484 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.623 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.479 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.586 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.656 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.530 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.422 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.518 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.565 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.426 |
MOD_PKB_1 | 517 | 525 | PF00069 | 0.569 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.482 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.578 |
MOD_Plk_2-3 | 536 | 542 | PF00069 | 0.494 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.615 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.524 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.503 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.412 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.569 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.502 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.565 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.539 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.664 |
MOD_SUMO_rev_2 | 382 | 391 | PF00179 | 0.440 |
TRG_DiLeu_BaEn_1 | 18 | 23 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_2 | 535 | 541 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 290 | 295 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 58 | 63 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 165 | 167 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 533 | 535 | PF00400 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V6 | Leptomonas seymouri | 34% | 99% |
A0A3Q8IVE9 | Leishmania donovani | 89% | 100% |
A4HN10 | Leishmania braziliensis | 69% | 100% |
A4IBN3 | Leishmania infantum | 90% | 100% |
E9B6M2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |