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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8IDU9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 547 | 549 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.456 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 307 | PF00134 | 0.389 |
DOC_MAPK_DCC_7 | 265 | 275 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 98 | 106 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 286 | 294 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 378 | 386 | PF00069 | 0.443 |
DOC_PP1_SILK_1 | 292 | 297 | PF00149 | 0.450 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.389 |
DOC_PP4_FxxP_1 | 556 | 559 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.407 |
DOC_USP7_MATH_2 | 211 | 217 | PF00917 | 0.566 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 360 | 366 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 459 | 464 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 141 | 156 | PF00022 | 0.457 |
LIG_APCC_ABBA_1 | 549 | 554 | PF00400 | 0.436 |
LIG_APCC_ABBAyCdc20_2 | 548 | 554 | PF00400 | 0.459 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_1 | 622 | 626 | PF00533 | 0.638 |
LIG_deltaCOP1_diTrp_1 | 486 | 490 | PF00928 | 0.393 |
LIG_eIF4E_1 | 506 | 512 | PF01652 | 0.445 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.381 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.390 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.340 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.660 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.623 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.423 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.602 |
LIG_FHA_2 | 620 | 626 | PF00498 | 0.526 |
LIG_LIR_Apic_2 | 401 | 405 | PF02991 | 0.324 |
LIG_LIR_Apic_2 | 553 | 559 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 252 | 261 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 385 | 395 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 417 | 425 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 449 | 458 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 504 | 513 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 417 | 422 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 520 | 525 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.485 |
LIG_Pex14_1 | 415 | 419 | PF04695 | 0.438 |
LIG_SH2_CRK | 522 | 526 | PF00017 | 0.438 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 87 | 90 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 613 | 617 | PF00017 | 0.581 |
LIG_SH2_STAT3 | 318 | 321 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.400 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.517 |
LIG_SUMO_SIM_anti_2 | 469 | 474 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.410 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.654 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.649 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.427 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.360 |
LIG_TRAF2_1 | 356 | 359 | PF00917 | 0.379 |
LIG_TRFH_1 | 556 | 560 | PF08558 | 0.447 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.344 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.392 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.703 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.701 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.692 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.814 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.696 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.394 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.343 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.365 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.414 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.677 |
MOD_Cter_Amidation | 161 | 164 | PF01082 | 0.500 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.672 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.750 |
MOD_GlcNHglycan | 353 | 358 | PF01048 | 0.409 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.632 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.504 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.554 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.734 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.578 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.449 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.484 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.511 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.436 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.601 |
MOD_LATS_1 | 134 | 140 | PF00433 | 0.532 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.552 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.475 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.450 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.435 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.411 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.317 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.448 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.637 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.369 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.509 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.376 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.731 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.436 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.342 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.434 |
MOD_PIKK_1 | 533 | 539 | PF00454 | 0.445 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.611 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.510 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.689 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.491 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.529 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.360 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.384 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.451 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.442 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.374 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.436 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.455 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.671 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.546 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.395 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.657 |
MOD_SUMO_rev_2 | 539 | 549 | PF00179 | 0.536 |
TRG_AP2beta_CARGO_1 | 417 | 426 | PF09066 | 0.452 |
TRG_DiLeu_BaEn_4 | 252 | 258 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_4 | 553 | 559 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 507 | 512 | PF01217 | 0.378 |
TRG_DiLeu_LyEn_5 | 269 | 274 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.384 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 540 | 542 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 19 | 24 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 500 | 504 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 510 | 514 | PF00026 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P278 | Leptomonas seymouri | 66% | 100% |
A0A0S4IQ65 | Bodo saltans | 31% | 88% |
A0A1X0NYR6 | Trypanosomatidae | 46% | 100% |
A4HGE6 | Leishmania braziliensis | 85% | 100% |
A4I3J2 | Leishmania infantum | 99% | 100% |
E9AZR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q8G5 | Leishmania major | 95% | 100% |