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: A0A3S7X8E6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.439 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.373 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.283 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.582 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.420 |
DEG_SPOP_SBC_1 | 405 | 409 | PF00917 | 0.615 |
DOC_ANK_TNKS_1 | 324 | 331 | PF00023 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 182 | 185 | PF00134 | 0.355 |
DOC_MAPK_DCC_7 | 180 | 188 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 9 | 18 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 12 | 20 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 180 | 188 | PF00069 | 0.428 |
DOC_PP1_RVXF_1 | 234 | 241 | PF00149 | 0.425 |
DOC_PP1_RVXF_1 | 263 | 270 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 361 | 367 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.347 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.355 |
DOC_PP2B_LxvP_1 | 473 | 476 | PF13499 | 0.644 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.515 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 291 | 296 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 325 | 329 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 388 | 397 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.355 |
LIG_Actin_WH2_2 | 252 | 267 | PF00022 | 0.361 |
LIG_Actin_WH2_2 | 383 | 400 | PF00022 | 0.569 |
LIG_AP2alpha_1 | 307 | 311 | PF02296 | 0.357 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.409 |
LIG_Clathr_ClatBox_1 | 111 | 115 | PF01394 | 0.361 |
LIG_CtBP_PxDLS_1 | 439 | 443 | PF00389 | 0.579 |
LIG_deltaCOP1_diTrp_1 | 105 | 110 | PF00928 | 0.311 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.413 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.444 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.365 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.255 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.604 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.632 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.621 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.494 |
LIG_LIR_Gen_1 | 191 | 198 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 427 | 438 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 44 | 51 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 367 | 371 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.401 |
LIG_MLH1_MIPbox_1 | 307 | 311 | PF16413 | 0.412 |
LIG_MYND_3 | 380 | 384 | PF01753 | 0.562 |
LIG_Pex14_1 | 454 | 458 | PF04695 | 0.562 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.317 |
LIG_Pex14_2 | 307 | 311 | PF04695 | 0.357 |
LIG_REV1ctd_RIR_1 | 158 | 167 | PF16727 | 0.322 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.497 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.325 |
LIG_SUMO_SIM_par_1 | 115 | 123 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 27 | 32 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.294 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.650 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.380 |
LIG_UBA3_1 | 260 | 265 | PF00899 | 0.390 |
LIG_UBA3_1 | 38 | 47 | PF00899 | 0.378 |
LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.353 |
MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.408 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.370 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.379 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.392 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.525 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.649 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.503 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.478 |
MOD_CMANNOS | 107 | 110 | PF00535 | 0.504 |
MOD_CMANNOS | 365 | 368 | PF00535 | 0.369 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.672 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.589 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.649 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.541 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.570 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.301 |
MOD_GlcNHglycan | 416 | 420 | PF01048 | 0.498 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.374 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.601 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.730 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.451 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.388 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.293 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.377 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.248 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.599 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.681 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.647 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.471 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.601 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.299 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.393 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.369 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.432 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.517 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.350 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.335 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.383 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.293 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.353 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.327 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.293 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.340 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.406 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.499 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.383 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.562 |
MOD_Plk_2-3 | 27 | 33 | PF00069 | 0.438 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.343 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.282 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.571 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.361 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.385 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.408 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.511 |
TRG_DiLeu_BaEn_1 | 469 | 474 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 34 | 39 | PF01217 | 0.373 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.315 |
TRG_NES_CRM1_1 | 322 | 336 | PF08389 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P448 | Leptomonas seymouri | 33% | 96% |
A4HB48 | Leishmania braziliensis | 69% | 100% |
A4IA96 | Leishmania infantum | 99% | 100% |
E9B5B8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q2L5 | Leishmania major | 89% | 100% |