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: 3 |
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: Q4Q2L5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.485 |
CLV_MEL_PAP_1 | 267 | 273 | PF00089 | 0.572 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.675 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.563 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.472 |
DOC_ANK_TNKS_1 | 324 | 331 | PF00023 | 0.403 |
DOC_CYCLIN_yCln2_LP_2 | 182 | 185 | PF00134 | 0.362 |
DOC_MAPK_DCC_7 | 180 | 188 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 180 | 188 | PF00069 | 0.451 |
DOC_MAPK_RevD_3 | 7 | 22 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 234 | 241 | PF00149 | 0.501 |
DOC_PP1_RVXF_1 | 263 | 270 | PF00149 | 0.432 |
DOC_PP1_RVXF_1 | 361 | 367 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.413 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.362 |
DOC_PP2B_LxvP_1 | 473 | 476 | PF13499 | 0.680 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.521 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 291 | 296 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 304 | 311 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 325 | 329 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 348 | 358 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 388 | 397 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 460 | 468 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.377 |
LIG_Actin_WH2_2 | 252 | 267 | PF00022 | 0.377 |
LIG_Actin_WH2_2 | 383 | 400 | PF00022 | 0.624 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.480 |
LIG_Clathr_ClatBox_1 | 111 | 115 | PF01394 | 0.436 |
LIG_CtBP_PxDLS_1 | 439 | 443 | PF00389 | 0.639 |
LIG_deltaCOP1_diTrp_1 | 105 | 110 | PF00928 | 0.354 |
LIG_deltaCOP1_diTrp_1 | 420 | 430 | PF00928 | 0.553 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.406 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.527 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.417 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.624 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.612 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.338 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.689 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.479 |
LIG_LIR_Gen_1 | 190 | 198 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 427 | 438 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.686 |
LIG_MLH1_MIPbox_1 | 307 | 311 | PF16413 | 0.469 |
LIG_MYND_3 | 380 | 384 | PF01753 | 0.619 |
LIG_Pex14_1 | 454 | 458 | PF04695 | 0.589 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.366 |
LIG_Pex14_2 | 285 | 289 | PF04695 | 0.273 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.480 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.393 |
LIG_SUMO_SIM_par_1 | 115 | 123 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 184 | 191 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 27 | 32 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.325 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.674 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.447 |
LIG_UBA3_1 | 111 | 117 | PF00899 | 0.302 |
LIG_UBA3_1 | 260 | 265 | PF00899 | 0.383 |
LIG_UBA3_1 | 38 | 47 | PF00899 | 0.459 |
LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.418 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.403 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.494 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.355 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.475 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.546 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.719 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.459 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.435 |
MOD_CMANNOS | 107 | 110 | PF00535 | 0.541 |
MOD_CMANNOS | 365 | 368 | PF00535 | 0.453 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.697 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.638 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.520 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.601 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.677 |
MOD_GlcNHglycan | 416 | 420 | PF01048 | 0.553 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.447 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.632 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.716 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.483 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.446 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.482 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.741 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.666 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.406 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.476 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.521 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.319 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.408 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.517 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.435 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.621 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.428 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.417 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.436 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.401 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.471 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.346 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.591 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.365 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.525 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.621 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.610 |
MOD_Plk_2-3 | 27 | 33 | PF00069 | 0.472 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.397 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.502 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.646 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.380 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.391 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.412 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.523 |
TRG_DiLeu_BaEn_1 | 469 | 474 | PF01217 | 0.654 |
TRG_DiLeu_BaLyEn_6 | 34 | 39 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.420 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.342 |
TRG_NES_CRM1_1 | 322 | 336 | PF08389 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P448 | Leptomonas seymouri | 32% | 96% |
A0A3S7X8E6 | Leishmania donovani | 89% | 100% |
A4HB48 | Leishmania braziliensis | 68% | 100% |
A4IA96 | Leishmania infantum | 88% | 100% |
E9B5B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |