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: A4H7H8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.627 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.543 |
CLV_Separin_Metazoa | 385 | 389 | PF03568 | 0.504 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.441 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.521 |
DEG_SPOP_SBC_1 | 340 | 344 | PF00917 | 0.555 |
DOC_ANK_TNKS_1 | 257 | 264 | PF00023 | 0.389 |
DOC_CKS1_1 | 44 | 49 | PF01111 | 0.617 |
DOC_CYCLIN_yCln2_LP_2 | 228 | 234 | PF00134 | 0.359 |
DOC_MAPK_gen_1 | 207 | 216 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 29 | 37 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 395 | 402 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 196 | 203 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 29 | 37 | PF00069 | 0.482 |
DOC_MAPK_NFAT4_5 | 196 | 204 | PF00069 | 0.434 |
DOC_PP1_RVXF_1 | 304 | 310 | PF00149 | 0.459 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.646 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 338 | 346 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 388 | 394 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 417 | 423 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 6 | 11 | PF00244 | 0.581 |
LIG_Actin_WH2_2 | 163 | 181 | PF00022 | 0.319 |
LIG_Actin_WH2_2 | 199 | 214 | PF00022 | 0.269 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.511 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.447 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.432 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.510 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.486 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.692 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.364 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.594 |
LIG_FXI_DFP_1 | 191 | 195 | PF00024 | 0.522 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 347 | 356 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.396 |
LIG_MYND_1 | 47 | 51 | PF01753 | 0.661 |
LIG_NRBOX | 198 | 204 | PF00104 | 0.400 |
LIG_NRBOX | 351 | 357 | PF00104 | 0.347 |
LIG_PDZ_Class_3 | 463 | 468 | PF00595 | 0.561 |
LIG_Pex14_2 | 194 | 198 | PF04695 | 0.398 |
LIG_Rb_LxCxE_1 | 68 | 85 | PF01857 | 0.414 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.608 |
LIG_SH3_1 | 438 | 444 | PF00018 | 0.574 |
LIG_SH3_2 | 383 | 388 | PF14604 | 0.503 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.739 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.377 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.583 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.503 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.557 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.629 |
LIG_SUMO_SIM_anti_2 | 197 | 203 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 398 | 403 | PF11976 | 0.400 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.367 |
MOD_CDK_SPK_2 | 82 | 87 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.539 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.474 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.678 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.501 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.430 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.443 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.402 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.369 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.543 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.538 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.543 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.480 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.446 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.504 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.530 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.515 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.609 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.440 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.462 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.677 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.544 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.370 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.569 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.588 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.518 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.410 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.479 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.351 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.418 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.592 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.632 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.661 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.570 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.609 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.432 |
MOD_NEK2_2 | 251 | 256 | PF00069 | 0.306 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.361 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.695 |
MOD_PKA_1 | 417 | 423 | PF00069 | 0.433 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.347 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.498 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.420 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.544 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.320 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.430 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.467 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.305 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.518 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.543 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.464 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.553 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.559 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.453 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.771 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.626 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.723 |
TRG_DiLeu_BaEn_1 | 348 | 353 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_4 | 384 | 390 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 441 | 443 | PF00400 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 354 | 358 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B4 | Leptomonas seymouri | 43% | 69% |
A0A3Q8I8P4 | Leishmania donovani | 78% | 68% |
A4HVV9 | Leishmania infantum | 78% | 68% |
E9APL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 68% |
Q4QFW8 | Leishmania major | 77% | 100% |