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: A4H7E3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.765 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.766 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.709 |
CLV_PCSK_PC7_1 | 47 | 53 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.577 |
DEG_APCC_DBOX_1 | 236 | 244 | PF00400 | 0.493 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 181 | PF00134 | 0.793 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.801 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.668 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.637 |
DOC_PP4_FxxP_1 | 391 | 394 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.756 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.793 |
LIG_14-3-3_CanoR_1 | 315 | 325 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 355 | 365 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 41 | 49 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 410 | 416 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 419 | 428 | PF00244 | 0.457 |
LIG_14-3-3_CterR_2 | 485 | 488 | PF00244 | 0.810 |
LIG_Actin_WH2_2 | 75 | 92 | PF00022 | 0.516 |
LIG_APCC_ABBA_1 | 157 | 162 | PF00400 | 0.705 |
LIG_APCC_ABBA_1 | 204 | 209 | PF00400 | 0.616 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.553 |
LIG_Clathr_ClatBox_1 | 226 | 230 | PF01394 | 0.446 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.547 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.587 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.679 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.444 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.680 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.502 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.611 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.517 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.591 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.691 |
LIG_GBD_Chelix_1 | 227 | 235 | PF00786 | 0.550 |
LIG_KLC1_Yacidic_2 | 158 | 162 | PF13176 | 0.710 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.724 |
LIG_LIR_LC3C_4 | 223 | 228 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.665 |
LIG_MYND_1 | 87 | 91 | PF01753 | 0.531 |
LIG_NRBOX | 463 | 469 | PF00104 | 0.639 |
LIG_PDZ_Class_1 | 483 | 488 | PF00595 | 0.821 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.451 |
LIG_Rb_pABgroove_1 | 148 | 156 | PF01858 | 0.712 |
LIG_SH2_CRK | 21 | 25 | PF00017 | 0.616 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.744 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.719 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.744 |
LIG_SH2_STAT3 | 338 | 341 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.545 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.553 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.718 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.562 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.370 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 223 | 230 | PF11976 | 0.398 |
LIG_SUMO_SIM_anti_2 | 422 | 431 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 223 | 230 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 422 | 431 | PF11976 | 0.521 |
LIG_TRAF2_1 | 68 | 71 | PF00917 | 0.769 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.323 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.666 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.427 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.719 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.621 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.294 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.507 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.514 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.381 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.723 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.799 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.688 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.685 |
MOD_Cter_Amidation | 49 | 52 | PF01082 | 0.596 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.558 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.664 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.641 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.766 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.511 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.603 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.633 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.655 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.699 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.577 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.693 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.475 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.407 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.479 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.473 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.532 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.699 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.681 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.662 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.558 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.451 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.459 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.577 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.728 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.659 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.560 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.538 |
MOD_NEK2_2 | 382 | 387 | PF00069 | 0.801 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.719 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.562 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.548 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.663 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.594 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.533 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.632 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.648 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.702 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.766 |
MOD_Plk_2-3 | 9 | 15 | PF00069 | 0.506 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.670 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.269 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.783 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.494 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.553 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.646 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.528 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.579 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.689 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.789 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_1 | 463 | 468 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_4 | 61 | 67 | PF01217 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 84 | 89 | PF01217 | 0.756 |
TRG_DiLeu_LyEn_5 | 352 | 357 | PF01217 | 0.531 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.727 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 355 | 360 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.466 |
TRG_PTS1 | 485 | 488 | PF00515 | 0.730 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K4 | Leptomonas seymouri | 48% | 83% |
A0A3S7WSN4 | Leishmania donovani | 75% | 100% |
A4HVT3 | Leishmania infantum | 75% | 100% |
E9APH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QG00 | Leishmania major | 74% | 100% |