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: 2, no: 4 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AMT9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.786 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.721 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.631 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 452 | 454 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.595 |
CLV_PCSK_PC7_1 | 427 | 433 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.748 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.565 |
DOC_CYCLIN_yCln2_LP_2 | 302 | 308 | PF00134 | 0.638 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.643 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.829 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 319 | 323 | PF12436 | 0.600 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.629 |
DOC_USP7_UBL2_3 | 448 | 452 | PF12436 | 0.596 |
DOC_USP7_UBL2_3 | 455 | 459 | PF12436 | 0.608 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.636 |
DOC_USP7_UBL2_3 | 471 | 475 | PF12436 | 0.540 |
DOC_USP7_UBL2_3 | 499 | 503 | PF12436 | 0.618 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 240 | 247 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 263 | 269 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 325 | 334 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 432 | 436 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 477 | 485 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 486 | 495 | PF00244 | 0.640 |
LIG_Clathr_ClatBox_1 | 86 | 90 | PF01394 | 0.621 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.473 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.518 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.750 |
LIG_LIR_LC3C_4 | 83 | 88 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.538 |
LIG_NRP_CendR_1 | 514 | 515 | PF00754 | 0.656 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.527 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.542 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.499 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.711 |
LIG_SH3_4 | 464 | 471 | PF00018 | 0.698 |
LIG_SH3_4 | 499 | 506 | PF00018 | 0.502 |
LIG_SH3_CIN85_PxpxPR_1 | 357 | 362 | PF14604 | 0.526 |
LIG_SUMO_SIM_par_1 | 85 | 92 | PF11976 | 0.616 |
MOD_CDK_SPK_2 | 353 | 358 | PF00069 | 0.656 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.656 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.594 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.553 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.447 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.692 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.685 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.674 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.493 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.441 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.653 |
MOD_DYRK1A_RPxSP_1 | 363 | 367 | PF00069 | 0.532 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.641 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.544 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.677 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.596 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.504 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.649 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.490 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.509 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.621 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.550 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.561 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.622 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.519 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.641 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.650 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.687 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.598 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.638 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.453 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.434 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.480 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.656 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.586 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.483 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.695 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.459 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.434 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.465 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.692 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.478 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.457 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.620 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.509 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.640 |
MOD_PIKK_1 | 64 | 70 | PF00454 | 0.492 |
MOD_PK_1 | 431 | 437 | PF00069 | 0.517 |
MOD_PK_1 | 481 | 487 | PF00069 | 0.654 |
MOD_PKA_1 | 325 | 331 | PF00069 | 0.454 |
MOD_PKA_1 | 373 | 379 | PF00069 | 0.648 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.525 |
MOD_PKA_1 | 471 | 477 | PF00069 | 0.588 |
MOD_PKA_1 | 504 | 510 | PF00069 | 0.584 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.434 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.640 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.527 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.716 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.712 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.624 |
MOD_PKB_1 | 183 | 191 | PF00069 | 0.548 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.677 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.436 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.530 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.653 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.526 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.604 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.562 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.484 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.638 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.644 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 434 | 440 | PF00179 | 0.515 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.627 |
TRG_NLS_Bipartite_1 | 325 | 343 | PF00514 | 0.460 |
TRG_NLS_MonoCore_2 | 429 | 434 | PF00514 | 0.508 |
TRG_NLS_MonoExtC_3 | 337 | 342 | PF00514 | 0.513 |
TRG_NLS_MonoExtC_3 | 430 | 436 | PF00514 | 0.539 |
TRG_NLS_MonoExtN_4 | 338 | 343 | PF00514 | 0.506 |
TRG_NLS_MonoExtN_4 | 427 | 434 | PF00514 | 0.570 |
TRG_NLS_MonoExtN_4 | 500 | 507 | PF00514 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW1 | Leptomonas seymouri | 43% | 100% |
A0A3Q8I7H5 | Leishmania donovani | 80% | 100% |
A4H5N7 | Leishmania braziliensis | 67% | 100% |
A4HU09 | Leishmania infantum | 80% | 100% |
Q4QHT6 | Leishmania major | 80% | 94% |