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: E9AHI3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.593 |
CLV_PCSK_PC7_1 | 200 | 206 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.621 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.675 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.746 |
DOC_CKS1_1 | 404 | 409 | PF01111 | 0.760 |
DOC_CYCLIN_RxL_1 | 353 | 365 | PF00134 | 0.697 |
DOC_MAPK_MEF2A_6 | 88 | 97 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 364 | 371 | PF00149 | 0.739 |
DOC_PP2B_LxvP_1 | 361 | 364 | PF13499 | 0.746 |
DOC_PP2B_LxvP_1 | 412 | 415 | PF13499 | 0.643 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.599 |
DOC_SPAK_OSR1_1 | 290 | 294 | PF12202 | 0.440 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 427 | 431 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.775 |
LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.573 |
LIG_Actin_WH2_2 | 2 | 20 | PF00022 | 0.681 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 427 | 431 | PF00533 | 0.508 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.663 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.533 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.628 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.586 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.489 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.724 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.601 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.727 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.402 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.632 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.741 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.552 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.745 |
LIG_LIR_Gen_1 | 282 | 291 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.425 |
LIG_MYND_1 | 411 | 415 | PF01753 | 0.568 |
LIG_RPA_C_Fungi | 285 | 297 | PF08784 | 0.507 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.551 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.622 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.636 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.666 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 320 | 326 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 320 | 326 | PF11976 | 0.627 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.614 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.525 |
MOD_CDK_SPK_2 | 231 | 236 | PF00069 | 0.706 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.551 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.638 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.618 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.589 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.657 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.592 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.770 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.484 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.601 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.742 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.552 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.790 |
MOD_DYRK1A_RPxSP_1 | 297 | 301 | PF00069 | 0.614 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.703 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.769 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.367 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.621 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.478 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.527 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.733 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.593 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.763 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.642 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.611 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.536 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.556 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.622 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.674 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.578 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.658 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.595 |
MOD_N-GLC_2 | 246 | 248 | PF02516 | 0.592 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.457 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.650 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.660 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.509 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.595 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.583 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.436 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.477 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.509 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.443 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.712 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.749 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.593 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.698 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.532 |
MOD_PKB_1 | 44 | 52 | PF00069 | 0.611 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.482 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.417 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.607 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.684 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.711 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.527 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.411 |
MOD_Plk_2-3 | 79 | 85 | PF00069 | 0.689 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.451 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.533 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.680 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.742 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.539 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.714 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.690 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.631 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.759 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.589 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.608 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.523 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.673 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.772 |
TRG_DiLeu_BaLyEn_6 | 225 | 230 | PF01217 | 0.669 |
TRG_DiLeu_BaLyEn_6 | 408 | 413 | PF01217 | 0.640 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I162 | Leptomonas seymouri | 44% | 73% |
A0A3Q8IR74 | Leishmania donovani | 99% | 100% |
E9ADT9 | Leishmania major | 89% | 100% |
E9AIT6 | Leishmania braziliensis | 70% | 100% |
E9ALZ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |