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: E9B3I6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 563 | 567 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.467 |
CLV_PCSK_PC7_1 | 381 | 387 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.284 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.385 |
DEG_APCC_DBOX_1 | 456 | 464 | PF00400 | 0.398 |
DEG_SCF_FBW7_1 | 539 | 546 | PF00400 | 0.538 |
DEG_SPOP_SBC_1 | 176 | 180 | PF00917 | 0.446 |
DOC_ANK_TNKS_1 | 187 | 194 | PF00023 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 568 | 574 | PF00134 | 0.540 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 227 | 235 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 569 | 576 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 588 | 597 | PF00069 | 0.287 |
DOC_PP2B_LxvP_1 | 568 | 571 | PF13499 | 0.568 |
DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.328 |
DOC_SPAK_OSR1_1 | 140 | 144 | PF12202 | 0.265 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.619 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.346 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 123 | 132 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 252 | 257 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 300 | 307 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 335 | 343 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 482 | 487 | PF00244 | 0.445 |
LIG_Actin_WH2_2 | 307 | 323 | PF00022 | 0.362 |
LIG_Actin_WH2_2 | 376 | 391 | PF00022 | 0.414 |
LIG_Actin_WH2_2 | 466 | 484 | PF00022 | 0.415 |
LIG_APCC_ABBA_1 | 367 | 372 | PF00400 | 0.441 |
LIG_APCC_ABBAyCdc20_2 | 165 | 171 | PF00400 | 0.372 |
LIG_BRCT_BRCA1_1 | 178 | 182 | PF00533 | 0.390 |
LIG_Clathr_ClatBox_1 | 436 | 440 | PF01394 | 0.278 |
LIG_deltaCOP1_diTrp_1 | 251 | 256 | PF00928 | 0.399 |
LIG_deltaCOP1_diTrp_1 | 605 | 610 | PF00928 | 0.468 |
LIG_eIF4E_1 | 229 | 235 | PF01652 | 0.328 |
LIG_EVH1_1 | 207 | 211 | PF00568 | 0.391 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.532 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.310 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.328 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.453 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.603 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.384 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.665 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.395 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.415 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.627 |
LIG_GBD_Chelix_1 | 466 | 474 | PF00786 | 0.275 |
LIG_LIR_Apic_2 | 179 | 185 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 281 | 287 | PF02991 | 0.320 |
LIG_LIR_Apic_2 | 38 | 43 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 432 | 441 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 445 | 456 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 489 | 499 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 445 | 451 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.443 |
LIG_MAD2 | 123 | 131 | PF02301 | 0.456 |
LIG_NRBOX | 465 | 471 | PF00104 | 0.364 |
LIG_PCNA_yPIPBox_3 | 292 | 304 | PF02747 | 0.402 |
LIG_PCNA_yPIPBox_3 | 55 | 69 | PF02747 | 0.384 |
LIG_Pex14_1 | 434 | 438 | PF04695 | 0.339 |
LIG_Pex14_2 | 444 | 448 | PF04695 | 0.416 |
LIG_PTB_Apo_2 | 88 | 95 | PF02174 | 0.385 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.331 |
LIG_SH2_PTP2 | 40 | 43 | PF00017 | 0.325 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 591 | 595 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.364 |
LIG_SH3_2 | 208 | 213 | PF14604 | 0.367 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.412 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.472 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.389 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.441 |
LIG_SUMO_SIM_anti_2 | 230 | 237 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 596 | 601 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 230 | 237 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 465 | 471 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 513 | 520 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 594 | 601 | PF11976 | 0.368 |
LIG_UBA3_1 | 50 | 55 | PF00899 | 0.429 |
MOD_CDK_SPxxK_3 | 71 | 78 | PF00069 | 0.345 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.409 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.538 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.431 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.498 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.428 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.351 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.468 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.451 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.431 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.408 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.404 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.348 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.557 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.368 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.450 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.498 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.314 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.418 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.289 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.404 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.584 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.531 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.399 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.445 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.397 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.567 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.426 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.486 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.628 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.656 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.624 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.286 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.450 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.362 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.436 |
MOD_N-GLC_2 | 21 | 23 | PF02516 | 0.481 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.544 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.415 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.474 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.399 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.459 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.567 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.528 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.581 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.426 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.449 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.427 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.383 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.438 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.427 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.605 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.368 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.483 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.304 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.595 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.367 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.390 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.414 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.430 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.466 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.493 |
MOD_Plk_1 | 591 | 597 | PF00069 | 0.392 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.452 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.349 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.376 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.342 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.467 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.424 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.394 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.292 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.576 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.416 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.603 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.605 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.473 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.346 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 110 | 115 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 283 | 288 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 386 | 390 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P687 | Leptomonas seymouri | 43% | 67% |
A0A3S7X6C3 | Leishmania donovani | 85% | 100% |
A4HL45 | Leishmania braziliensis | 74% | 100% |
A4I8M4 | Leishmania infantum | 85% | 100% |
Q4Q4L4 | Leishmania major | 86% | 100% |