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: A4HCK7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.566 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.434 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 564 | 566 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 604 | 606 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 584 | 588 | PF00082 | 0.297 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.486 |
DEG_APCC_DBOX_1 | 604 | 612 | PF00400 | 0.339 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.654 |
DEG_SPOP_SBC_1 | 186 | 190 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 504 | 508 | PF00917 | 0.444 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.283 |
DOC_CYCLIN_RxL_1 | 414 | 422 | PF00134 | 0.496 |
DOC_MAPK_gen_1 | 321 | 330 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 343 | 353 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 417 | 425 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 346 | 353 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 232 | 239 | PF00149 | 0.387 |
DOC_PP1_RVXF_1 | 516 | 523 | PF00149 | 0.361 |
DOC_PP2B_LxvP_1 | 126 | 129 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.543 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 178 | 186 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 386 | 390 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 418 | 424 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 436 | 440 | PF00244 | 0.218 |
LIG_14-3-3_CanoR_1 | 502 | 510 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 528 | 536 | PF00244 | 0.378 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.501 |
LIG_APCC_ABBA_1 | 304 | 309 | PF00400 | 0.398 |
LIG_APCC_ABBA_1 | 519 | 524 | PF00400 | 0.425 |
LIG_APCC_ABBAyCdc20_2 | 518 | 524 | PF00400 | 0.270 |
LIG_CaM_IQ_9 | 260 | 275 | PF13499 | 0.417 |
LIG_Clathr_ClatBox_1 | 423 | 427 | PF01394 | 0.391 |
LIG_deltaCOP1_diTrp_1 | 427 | 435 | PF00928 | 0.293 |
LIG_FAT_LD_1 | 13 | 21 | PF03623 | 0.398 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.454 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.556 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.498 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.435 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.414 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.423 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.497 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.400 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.341 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.311 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.533 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.379 |
LIG_GBD_Chelix_1 | 228 | 236 | PF00786 | 0.260 |
LIG_IBAR_NPY_1 | 23 | 25 | PF08397 | 0.510 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 335 | 344 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 427 | 434 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 465 | 472 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 335 | 339 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 398 | 402 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 465 | 469 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 598 | 602 | PF02991 | 0.369 |
LIG_NRBOX | 12 | 18 | PF00104 | 0.404 |
LIG_NRBOX | 419 | 425 | PF00104 | 0.499 |
LIG_PDZ_Class_2 | 612 | 617 | PF00595 | 0.490 |
LIG_Pex14_1 | 385 | 389 | PF04695 | 0.470 |
LIG_SH2_PTP2 | 162 | 165 | PF00017 | 0.384 |
LIG_SH2_PTP2 | 325 | 328 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.266 |
LIG_SH2_STAT3 | 577 | 580 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.217 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.450 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.547 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.402 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.507 |
LIG_SUMO_SIM_anti_2 | 118 | 125 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 188 | 197 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 42 | 49 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 422 | 427 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 422 | 427 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 89 | 97 | PF11976 | 0.388 |
LIG_UBA3_1 | 443 | 452 | PF00899 | 0.281 |
LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.316 |
MOD_CDK_SPxxK_3 | 589 | 596 | PF00069 | 0.476 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.519 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.448 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.587 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.626 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.526 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.451 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.572 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.563 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.297 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.499 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.374 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.467 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.497 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.558 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.429 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.691 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.448 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.536 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.452 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.324 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.417 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.382 |
MOD_GlcNHglycan | 495 | 499 | PF01048 | 0.538 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.438 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.494 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.419 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.603 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.581 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.643 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.506 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.425 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.519 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.612 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.569 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.305 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.552 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.306 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.308 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.496 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.372 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.481 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.503 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.518 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.573 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.325 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.252 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.451 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.420 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.666 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.324 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.535 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.540 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.522 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.668 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.385 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.529 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.377 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.584 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.468 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.415 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.519 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.667 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.320 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.258 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.453 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.471 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.469 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.481 |
MOD_SUMO_rev_2 | 590 | 597 | PF00179 | 0.532 |
TRG_DiLeu_BaEn_1 | 532 | 537 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_4 | 359 | 365 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 415 | 420 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 515 | 520 | PF01217 | 0.262 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.233 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.322 |
TRG_NES_CRM1_1 | 231 | 245 | PF08389 | 0.309 |
TRG_Pf-PMV_PEXEL_1 | 576 | 580 | PF00026 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 584 | 588 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDK4 | Leptomonas seymouri | 45% | 100% |
A0A1X0NU19 | Trypanosomatidae | 28% | 100% |
A0A3R7K6E0 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H7B4 | Leishmania donovani | 76% | 100% |
A4I025 | Leishmania infantum | 76% | 100% |
E9AVZ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QBI1 | Leishmania major | 76% | 100% |